| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs9688173 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203921 | cggggcctgtcaggg[G/T]gtagggggctagggg | 23092 |
| rs9715951 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958925 | aaaaaaaaaaGAAAA[A/G]AAAAAAGAAAGGAAA | 23092 |
| rs9763697 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988680 | tgtcccagagattct[A/G]gtatgttgtgtcttt | 23092 |
| rs9918291 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152185 | tgcatttgtcaaaac[C/T]catagaacacaaaga | 23092 |
| rs10035861 | snp | A/G | 0.340784 | 0.232934 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105513 | GAAGCATTTTATTGC[A/G]TAAGTTTTCTTCTGT | 23092 |
| rs10036154 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163726 | aaagtgctgggatta[C/T]aggcatgagccacca | 23092 |
| rs10036365 | snp | A/G | 0.20511 | 0.245937 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844257 | ggtttcgccatatcg[A/G]ccaggctggtctcaa | 23092 |
| rs10038512 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220415 | GCCTGGCTCTGTGCC[A/G]AGTGCTTTATCCACA | 23092 |
| rs10039856 | snp | C/T | 0.443464 | 0.15834 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872984 | ACCTAGGGGAAATTA[C/T]TGTTGAGTCAGACTT | 23092 |
| rs10039984 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029690 | ctgagattacagttg[A/G]gagccagggtgctca | 23092 |
| rs10040804 | snp | C/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862160 | ACAGGGAGGTGACAG[C/G]CCTTGGCTTCTCTTT | 23092 |
| rs10042004 | snp | C/G | 0.240478 | 0.249819 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941283 | CATCTGTTATTTTTT[C/G]ACTTTTTAGTAATAG | 23092 |
| rs10042057 | snp | C/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169632 | taaccaatctttgtg[C/G]ccaggggtataagtg | 23092 |
| rs10042074 | snp | C/T | 0.479984 | 0.0980171 | intron-variant, splice-donor-variant | ARHGAP26 | GRCh38.p7 | 5:142771377 | CCCCTTGGGAAAAGG[C/T]GGGTTGTGACTGCTT | 23092 |
| rs10042662 | snp | G/T | 0.109461 | 0.206758 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794347 | GGATGATTTCCCAGA[G/T]GAATACTGGGGTGCT | 23092 |
| rs10042753 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212867 | atactgatgcctggc[C/T]gggcgcggtggctca | 23092 |
| rs10042944 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978685 | actttccacctcttg[A/G]acaccctataaatgt | 23092 |
| rs10043021 | snp | C/G | 0.316485 | 0.240998 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812118 | ACTGCCTTTTCCCCC[C/G]AGTGCTTCCTCTTCG | 23092 |
| rs10044036 | snp | C/T | 0.40263 | 0.198 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858554 | TATCATTCTTCTGAC[C/T]GAACTCTTAAAAAAG | 23092 |
| rs10044668 | snp | A/G | 0.123452 | 0.215605 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102863 | TGCTTTGTCCTTACA[A/G]CATCCCAGTGCCTCT | 23092 |
| rs10044789 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103312 | GATGCTGGAGAGGAT[A/G]TGGAGAAATAGGAAC | 23092 |
| rs10045128 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041088 | TGGGCCTGGAACTAA[C/T]AGGAGAAAAATCATT | 23092 |
| rs10045187 | snp | A/G | 0.191147 | 0.242974 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837920 | CTTTCATTTTTCCCT[A/G]CAGGGATATTGGCAG | 23092 |
| rs10045199 | snp | C/T | 0.377187 | 0.215229 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121263 | CTTACACTGTCATGA[C/T]GATGAAGTTGCTGGT | 23092 |
| rs10045315 | snp | A/G | 0.348794 | 0.229651 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109161 | GGTAGCAGGTAACTC[A/G]CACCTAGAAGCTCTT | 23092 |
| rs10045391 | snp | A/G | 0.306679 | 0.24349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038578 | TACAAAATCAGAAAC[A/G]GGCCAAATGTCTCAA | 23092 |
| rs10045402 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815260 | tggccaggctggtct[C/T]aaactcctgacctta | 23092 |
| rs10045807 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939314 | AAGTAGAGTTACTCT[G/T]CTGTGGCTACTGCAG | 23092 |
| rs10050379 | snp | A/G | 0.335788 | 0.23482 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013152 | AGTACCAATTAAGCT[A/G]AATATCAACCTCTCT | 23092 |
| rs10051655 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910405 | TGTCTTCTCGATTGT[A/G]TAGAGGAATCATGTG | 23092 |
| rs10051682 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048918 | actccatctcaaaaa[A/G]gaaaaaaaaaaaaaa | 23092 |
| rs10052788 | snp | C/T | 0.235273 | 0.249566 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993324 | acaggcgcccgccac[C/T]gcgcccggctaattt | 23092 |
| rs10053874 | snp | A/G | 0.151001 | 0.229563 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840638 | GTGGTAGTTGTCATC[A/G]TCTTATTTGAGCCTA | 23092 |
| rs10054044 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810836 | TAAGTAACCATAAGC[A/G]TTGATATGTAAACTC | 23092 |
| rs10054425 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220751 | CTTTGGAGGCCAACT[A/G]ATAGATGTTTAACCT | 23092 |
| rs10054462 | snp | A/G | 0.256061 | 0.249927 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984943 | aaaaagcggtcagac[A/G]gccttaaacaagacc | 23092 |
| rs10056044 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047513 | gatgttgaattgctg[A/G]gtcaaggtatgtacg | 23092 |
| rs10056296 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794491 | TAGCATGGTTGTTAC[C/T]CACATTTGAAAATTA | 23092 |
| rs10056505 | snp | A/G | 0.235854 | 0.249599 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018122 | tctattcataggcct[A/G]ttagtttactgggtt | 23092 |
| rs10056531 | snp | C/T | 0.246769 | 0.249979 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899529 | TTGCCCCGTGGACAG[C/T]TGACCCCTCTTATTT | 23092 |
| rs10057627 | snp | A/T | 0.298905 | 0.24517 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845363 | GATGAGGAAGCTGAG[A/T]CTCAGAGCAGTTAAG | 23092 |
| rs10057800 | snp | A/G | 0.414741 | 0.188044 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058657 | TATAGTCCATACTTT[A/G]CTATGCCATTAGGGT | 23092 |
| rs10057931 | snp | C/T | 0.215446 | 0.2476 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961406 | CTGAGGTGGGAGGAT[C/T]GATCGAGGTTGGGAG | 23092 |
| rs10058485 | snp | A/G | 0.45692 | 0.1403 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048919 | CTCCATCTCAAAAAA[A/G]AAAAAAAAAAAAAAA | 23092 |
| rs10058887 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222995 | TAAAACACTGTTTAT[A/G]TAAGATCCAATCTCT | 23092 |
| rs10058923 | snp | A/G | 0.155987 | 0.23165 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097807 | AGCCTGGGTGACAGA[A/G]CGAGACTCCAACTCA | 23092 |
| rs10059193 | snp | A/C | 0.258843 | 0.249844 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916632 | CAAAACAAAACAAAA[A/C]AAAATTCAGGCTCCT | 23092 |
| rs10060327 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097531 | ATGTGAAAATTGCCT[C/T]ATGCAATggccgggc | 23092 |
| rs10061846 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832187 | GTGTTATCTGTTTCC[C/T]TCTAATAAAtgctat | 23092 |
| rs10062064 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832503 | catcttgtcttccag[C/T]ctccagaactgtgag | 23092 |
| rs10062088 | snp | A/T | 0.495095 | 0.0492773 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928248 | TTTTTTTTTTTTTTT[A/T]AAAACTCATTGCCTT | 23092 |
| rs10062094 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215932 | tgtgtgtaggttttt[A/G]tgagggcgtaggttt | 23092 |
| rs10062481 | snp | C/T | 0.215446 | 0.2476 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972765 | CCTATATATTTGCTA[C/T]GTTGTGTCCTTTGAC | 23092 |
| rs10062886 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845323 | aatgcttccgggtgg[A/G]tatttgttatcaccc | 23092 |
| rs10063491 | snp | A/G | 0.089084 | 0.191327 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070228 | TACATTTCCCTTCAT[A/G]ATAGAACTGCCACTT | 23092 |
| rs10064205 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091760 | tagtgctttaagaaa[G/T]acctgttgtgctttt | 23092 |
| rs10065158 | snp | A/G | 0.084728 | 0.187577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829829 | TTTTCCACTCATGAC[A/G]CTGAGGATGGTGTCA | 23092 |
| rs10065564 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830504 | TCAGTCTGTTTTTCC[A/G]TAATTGTGATGACCT | 23092 |
| rs10065814 | snp | C/T | 0.105924 | 0.204309 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110417 | ACCTTGCACTTTCTT[C/T]GTTGGGTAGAAAGTC | 23092 |
| rs10068940 | snp | C/T | 0.240478 | 0.249819 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940892 | ccatcctggctaaca[C/T]ggtgaaacctggtct | 23092 |
| rs10070792 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218251 | TTCCCGTCACAGGGC[C/T]GTTGTACTTGCACTA | 23092 |
| rs10071641 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811794 | TATGATACTCTTGTG[C/T]GCAGCCTTGCACCAG | 23092 |
| rs10071771 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201351 | TCATCTGCTAAAATT[A/G]TAGTTATAAAATCAT | 23092 |
| rs10072246 | snp | A/G | 0.084728 | 0.187577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830351 | TTAGTGCAATTGAGA[A/G]TGACTATGGCAATGA | 23092 |
| rs10072257 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070999 | ggaccacaaaagacc[A/G]tgaatagcaaaagca | 23092 |
| rs10072911 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832590 | CTTATTTCAGGTCTT[C/T]TGTGTGCCTGGCACA | 23092 |
| rs10074183 | snp | A/G | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227007 | GTCTTGACTGCAGAG[A/G]CTCCAAAAGCATTCA | 23092 |
| rs10074187 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131989 | AAACTTGTTTTTTGG[A/G]GTTCCAGCTGCTCGG | 23092 |
| rs10075062 | snp | C/T | 0.487933 | 0.0767327 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134566 | TCTTTTACTCCACCT[C/T]TCATGGTGCCTGGCA | 23092 |
| rs10075783 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843846 | tatggtgatgaagag[A/C]ctgagctttggcttc | 23092 |
| rs10076583 | snp | A/G | 0.033725 | 0.1254 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073244 | TAAAAAAGTTTAAAG[A/G]TAAGTTCCAAAGCAA | 23092 |
| rs10077444 | snp | C/T | 0.00211907 | 0.0324814 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120977 | GTACCTTTTCTTTTC[C/T]TTCCTCCCAGTGTTG | 23092 |
| rs10077909 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844935 | TTCCTCCCCTGCTCT[C/T]TGATGCCTGCTGAAC | 23092 |
| rs10078709 | snp | G/T | 0.0970103 | 0.197722 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810720 | TGATGTAATACCTAT[G/T]TCATTGTTGACCTAA | 23092 |
| rs10079523 | snp | A/C | 0.328382 | 0.237395 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112929 | TAAAAATGGGTGTAC[A/C]AATACTTCTTTGAGA | 23092 |
| rs10080138 | snp | C/T | 0.0368353 | 0.130617 | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961601 | ATATCAGCCTGTCAC[C/T]TGACCTATGGGTATT | 23092 |
| rs10085017 | snp | G/T | 0.0744748 | 0.178019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842756 | gaaattccctcaaca[G/T]ttcatttggaggagg | 23092 |
| rs10085147 | snp | A/C | 0.139903 | 0.224452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840451 | TGTTGTTGTTTTTTG[A/C]CTATTGTTAAATAGG | 23092 |
| rs10155562 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098901 | ttttaaacatgactt[C/T]gtgaaagtatagtat | 23092 |
| rs10213741 | snp | A/C | 0.0898077 | 0.191933 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060446 | ATTCAGAGGGGAAAA[A/C]AAGTATTGGGTGGGG | 23092 |
| rs10214187 | snp | A/G | 0.235564 | 0.249583 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933277 | GTTGAGCACATTTTT[A/G]CATGTTAGGCACAGG | 23092 |
| rs10214217 | snp | C/T | 0.106278 | 0.204558 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113376 | GTGTTTCCCCAGAAG[C/T]AGAGAACACTTTGCT | 23092 |
| rs10214251 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833700 | ATGTTTGGCTTTGGC[A/G]TTAGGGGCGGAGGCC | 23092 |
| rs10447227 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053335 | GGTTGCTCTCCAACT[A/C]AAAATGAGGTGCTAT | 23092 |
| rs10452526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016680 | tgcactccatcctgg[A/G]caatagactgagact | 23092 |
| rs10452527 | snp | A/G | 0.180064 | 0.240019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031489 | attgagggacttggt[A/G]ataatttggaatggg | 23092 |
| rs10452528 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031609 | CTGGGAGGAGCCAGT[G/T]AAAAGTATCTCAGAT | 23092 |
| rs10452529 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151803 | tctactaaaaatgca[A/G]aaaaattagctgggc | 23092 |
| rs10463357 | snp | G/T | 0.214843 | 0.247516 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073333 | GTGTTCTTTGGGATT[G/T]GACAGCTTGTTGAAA | 23092 |
| rs10476845 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804482 | AGCATAGGTTTGAAC[A/G]GAttttattttttat | 23092 |
| rs10476846 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823965 | CAGTGGTTTATAGAC[A/G]AATAACAAAGCAATG | 23092 |
| rs10477196 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818287 | AGGCTCCACTGGGCC[C/T]TGTTCTGGCCAGCCA | 23092 |
| rs10477197 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818467 | TTTTGGTGGCTGCAC[C/T]GTCTGCTGTCACTCT | 23092 |
| rs10477198 | snp | C/T | 0.084364 | 0.187256 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821200 | AGAGCGGGTGAATTA[C/T]TCACACATGGGCCAA | 23092 |
| rs10477199 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056717 | GCAGAAAGATTCTCT[A/C]TCAGATTTAAATCCA | 23092 |
| rs10477200 | snp | C/G/T | 0.0803491 | 0.183626 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071404 | tcaataaatggtact[C/G/T]ggaaaactggataat | 23092 |
| rs10477201 | snp | C/T | 0.105924 | 0.204309 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109517 | tggagtgcagtggtg[C/T]gatctcagctcactg | 23092 |
| rs10477202 | snp | G/T | 0.0879971 | 0.190408 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128966 | CACACATTACAGGGA[G/T]ACTCCTAATCCTTTT | 23092 |
| rs10477203 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184035 | TGAATAAAGGGGTAA[A/G]GTATTTAGATTCTGA | 23092 |
| rs10515517 | snp | A/G | 0.154661 | 0.231107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877348 | TTTTCTTAACATCCA[A/G]TTCGTGCTTCTGATC | 23092 |
| rs10515518 | snp | A/C | 0.125528 | 0.21681 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878026 | TCTGAAATAAGTGAT[A/C]TCCAAATTGAGAAAA | 23092 |
| rs10515519 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133544 | TTTAAGAAAGTTGTG[A/T]AGTAATTGTTAAGAA | 23092 |
| rs10515520 | snp | A/G | 0.272511 | 0.248984 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206727 | AAAATGCAAACAGGA[A/G]ATTATTTTCTCACCG | 23092 |
| rs10531678 | in-del | -/TAAT | 0.264906 | 0.249555 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189587 | TTTCCATTAGGATAA[-/TAAT]TAAAATATTATCAAA | 23092 |
| rs10543021 | in-del | -/GT | 0.479583 | 0.0989539 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896005 | ACCTAACTTCCAGCA[-/GT]GTGGTTTCAGTCAAG | 23092 |
| rs10550663 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779434 | AGGGTGGTGTGTGTG[-/TG]TGTGTGTGTGTTTTC | 23092 |
| rs10551710 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027176 | TCATGATTTTTTGTG[-/T]TTTTTTTTTTTTTGA | 23092 |
| rs10552247 | in-del | -/TA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948421 | TTAAATATATATATA[-/TA]TAATATGTATTTTAA | 23092 |
| rs10555676 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795048 | TCATATCTTCTTCTT[-/C]TTTTTTTTTAAAAAA | 23092 |
| rs10571226 | in-del | -/AC | 0.487368 | 0.0784625 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898176 | TATACACACACACAT[-/AC]ACACACACACACACA | 23092 |
| rs10571955 | in-del | -/ACAA | 0.356597 | 0.226135 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158875 | AAGATGTTATTGTCC[-/ACAA]ACAAACAAACAAACA | 23092 |
| rs10587181 | in-del | -/TA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948423 | AAATATATATATATA[-/TA]ATATGTATTTTAATT | 23092 |
| rs10597676 | in-del | -/GG | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190028 | TGGAGGACAGAAGGA[-/GG]GGGGGGAAAAAAAAA | 23092 |
| rs10610584 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168476 | TTTTTTTTTTTTTTT[-/T]GCTCAAATTTTCTTC | 23092 |
| rs10650559 | in-del | -/AAAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154169 | AATATTAAAAAAAAA[-/AAAAA]AAAAGAGTTTCTGCT | 23092 |
| rs10655807 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787996 | TTATTAACCAATTCT[-/T]TTTTTTTTTTTTTTT | 23092 |
| rs10667047 | in-del | -/AAA/AAAA | 0.444 | 0.157683 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904525 | AAGAAAAAAAAAAAA[-/AAA/AAAA]GAGCCAAGAATACTC | 23092 |
| rs10672936 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056340 | TTTTTTTTTTTTTTT[-/T]GAGGGGAGGAGGATG | 23092 |
| rs10711586 | in-del | -/A | 0.427575 | 0.175975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076911 | CTTAGAGTTGTTTCT[-/A]AAGTTTTTAACATTA | 23092 |
| rs10718611 | in-del | -/A | 0.26078 | 0.249767 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142500 | TTTTAAGATTTTTTT[-/A]AAAAAAAAACATTGT | 23092 |
| rs10783184 | snp | G/T | 0.463989 | 0.129263 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020857 | GTGTTAGCCAGGATG[G/T]TCTCGATCTGCTGAC | 23092 |
| rs10875598 | snp | C/T | 0.46974 | 0.119223 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011593 | GCCGCTATGCCCTTC[C/T]TCAATAGCCACATGA | 23092 |
| rs10875599 | snp | C/T | 0.429538 | 0.173972 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020840 | AGAGACAGGGTTTCA[C/T]CGTGTTAGCCAGGAT | 23092 |
| rs10875600 | snp | A/G | 0.448323 | 0.15221 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105811 | CACCGGGGCGTTATG[A/G]GAAAGTAACGTGTAG | 23092 |
| rs10875601 | snp | A/G | 0.422944 | 0.180528 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109736 | caagccgccacaccc[A/G]gccATATCTCTCTCT | 23092 |
| rs10875602 | snp | G/T | 0.490119 | 0.0695896 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220148 | CTCAACTTGGAGCTT[G/T]GCTATAAAGCGGGAG | 23092 |
| rs11167792 | snp | G/T | 0.393619 | 0.204631 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797925 | CAAGCTCCAGTTGAT[G/T]TTCATGCTGCTGAGT | 23092 |
| rs11167795 | snp | G/T | 0.464096 | 0.129085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991902 | TTATCTTTGAAGCTT[G/T]CTCTTCATGAAGACT | 23092 |
| rs11167796 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006318 | TTTAGTGTTTTTTCT[G/T]TTTTTTTTTTTTTTT | 23092 |
| rs11167797 | snp | A/G | 0.46845 | 0.121572 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008630 | CAAATTTCCTTATGA[A/G]CCTATTTCCCCAGCA | 23092 |
| rs11167798 | snp | A/G | 0.463989 | 0.129263 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008660 | ATCTTTATTTTGTCC[A/G]GATTTTGATCCAAAG | 23092 |
| rs11167799 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076913 | TAGAGTTGTTTCTAA[A/G]GTTTTTAACATTATA | 23092 |
| rs11167800 | snp | A/G | 0.455144 | 0.142885 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090356 | gtttaacgtgtgaat[A/G]gaatatttgatccat | 23092 |
| rs11167801 | snp | C/T | 0.459801 | 0.135955 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090769 | ttcattcttgctctt[C/T]agtggtccgcagaac | 23092 |
| rs11167802 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092188 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCCCTCTCG | 23092 |
| rs11167803 | snp | C/T | 0.104149 | 0.203046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092544 | TTTTACATAAATTCT[C/T]CCCCCCCCACCTTTT | 23092 |
| rs11167804 | snp | G/T | 0.355096 | 0.226837 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122624 | agctgagcagaggag[G/T]ttggctttatagaca | 23092 |
| rs11167805 | snp | A/C/T | 0.137527 | 0.223271 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180636 | acatgtcttatatgg[A/C/T]ggcaggctagagaag | 23092 |
| rs11167806 | snp | A/G | 0.138886 | 0.22395 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180662 | agaagtgttaggagc[A/G]aagagggaagagtcc | 23092 |
| rs11167807 | snp | A/G | 0.361263 | 0.223876 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200342 | tcaggaatttatgct[A/G]aggaaacaattgaga | 23092 |
| rs11286150 | in-del | -/A | 0.497933 | 0.032082 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928889 | TCTGATATTTACTCC[-/A]ATTTCTCTTTCATTG | 23092 |
| rs11295663 | in-del | -/A | 0.443732 | 0.158012 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925092 | AACAGTTTAAAACTG[-/A]AAAAAATCTTTAACT | 23092 |
| rs11300501 | in-del | -/C | 0.00914312 | 0.0669923 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216413 | GAATTACTTACAAGG[-/C]CCTCCAGGGCCCAGT | 23092 |
| rs11313040 | in-del | -/G | 0.387832 | 0.208572 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014524 | ACGGTCTCGCTCAAA[-/G]GACTGGAGAGGCAAT | 23092 |
| rs11317162 | in-del | -/C | 0.487746 | 0.0773096 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964547 | TCTCTGTTTAAAACA[-/C]ACACACACACACACA | 23092 |
| rs11326621 | in-del | -/G | 0.0681886 | 0.171594 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051801 | ATTAGTTTGCTAAAT[-/G]TGGTTCATGCAACAG | 23092 |
| rs11331959 | in-del | -/T | 0.479984 | 0.0980171 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210897 | GTCTGAAGGGCACTG[-/T]TGACAGGAGCAGCCG | 23092 |
| rs11331984 | in-del | -/T | 0.491051 | 0.0662916 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213424 | GTCTATTCCCTCCCC[-/T]GGGGGTTGGAGAGCT | 23092 |
| rs11332182 | in-del | -/T | 0.449473 | 0.150701 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781365 | TTTGATATGGTTAAC[-/T]TTTTTTTTCTAAATA | 23092 |
| rs11338660 | in-del | -/T | 0.47852 | 0.101384 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905392 | ATGGGGATACAGCAC[-/T]TTTTTTTTAATTTTA | 23092 |
| rs11339754 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132878 | AAAAAAAAAAAAAAA[-/A]CTGTTATCTTCTGAA | 23092 |
| rs11347785 | in-del | -/T | 0.492966 | 0.0588865 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224108 | TACTGTATCTTTTAC[-/T]TTTTTTTTTTTGAAA | 23092 |
| rs11357774 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020656 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 23092 |
| rs11361288 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161027 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCTT | 23092 |
| rs11369150 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949232 | AGAGGAGAGAGAGAG[-/A]GAGAGAGAGAGAGAG | 23092 |
| rs11372661 | in-del | -/T | 0.328616 | 0.237317 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185347 | TGCCTGTTGTTTTTT[-/T]AACAATAAGTATGAA | 23092 |
| rs11373777 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088471 | TTGGACCAAATTGTT[-/A]AAAAAAAAAAAGTGG | 23092 |
| rs11375975 | in-del | -/T | 0.493013 | 0.058691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978748 | TTTTTTTTTTTTTTT[-/T]GTAAAAATTGAAAAT | 23092 |
| rs11388554 | snp | A/G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923880 | TTTTTTTTTTTTTTT[A/G/T]ATACGGAGTCCTGCT | 23092 |
| rs11389284 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923857 | ATTAGGATCAGATCC[-/T]TTTTTTTTTTTTTTT | 23092 |
| rs11397426 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791942 | GCAAAACCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 23092 |
| rs11408187 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118943 | TAAAAGTATAATAAT[-/A]AAAAAAAAAAAAAGA | 23092 |
| rs11419144 | in-del | -/A | 0.48818 | 0.0759629 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955125 | CACACACACACACAC[-/A]CCCCCATCTCTGCAC | 23092 |
| rs11422372 | in-del | -/C | 0.451732 | 0.147663 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891612 | AAGCTCTTAAGATGT[-/C]CAAGTAGCATATTGT | 23092 |
| rs11422894 | in-del | -/T/TT | 0.498481 | 0.027514 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160475 | TGTTGCTTTTGGTGG[-/T/TT]TTTTTTTTTCTTTCT | 23092 |
| rs11429323 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204075 | GTATAATTAAAAAAA[-/A]AAAAAATCACAGAAG | 23092 |
| rs11441015 | in-del | -/T/TC/TT | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160484 | TGGTGGTTTTTTTTT[-/T/TC/TT]CTTTCTTTTTTTTTC | 23092 |
| rs11462785 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022091 | GTTTTATTTCATTTA[-/T]TTTTTTTGAGACCCC | 23092 |
| rs11548701 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227858 | ATCGCTTTTTTTTTT[C/T]TCCTCAGTAAGCATA | 23092 |
| rs11738496 | snp | A/C | 0.0700422 | 0.173537 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782820 | ATGCTTAGCAGTGTA[A/C]GCAGGCCTGTGGTAA | 23092 |
| rs11738668 | snp | C/T | 0.463234 | 0.130503 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013181 | CTTAAAAAAAACTTA[C/T]TCTTCTGATTAGTAG | 23092 |
| rs11738817 | snp | C/T | 0.464203 | 0.128908 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992576 | GGGACTACAGGTACC[C/T]GCCACCATGCCCGGC | 23092 |
| rs11738829 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858673 | ATGAACAAAACAGTC[A/C]CGGCTACTGCCTGCC | 23092 |
| rs11738878 | snp | G/T | 0.201418 | 0.245234 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787692 | CCAAAAACCTGTATT[G/T]TTTCTTAGATAACAT | 23092 |
| rs11739101 | snp | G/T | 0.436123 | 0.166908 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076136 | TAACTAGGACTACAG[G/T]TGTGCGCCACCAGAC | 23092 |
| rs11739631 | snp | C/G | 0.156735 | 0.231952 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780815 | TGGTCTAGGGGACAC[C/G]TTGCCTATCATAGAA | 23092 |
| rs11740100 | snp | G/T | 0.0715223 | 0.175059 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114634 | TTGACTGCAGCTTAG[G/T]TACCCACCCACTTAC | 23092 |
| rs11740320 | snp | A/G | 0.424503 | 0.179021 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061494 | CAGCTGGTTTTCCCA[A/G]AATACTTATTGAGAA | 23092 |
| rs11742036 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167717 | TTTTGTTTTAACTGG[G/T]GCTGGGTTAAGAATT | 23092 |
| rs11742230 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031986 | GGCATCCTCTTCCCA[C/T]GTCTGTGGTTTTCCC | 23092 |
| rs11743602 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070234 | TCCCTTCATAATAGA[A/C]CTGCCACTTAAACTG | 23092 |
| rs11744069 | snp | C/T | 0.475259 | 0.108435 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003646 | AAGAGATCAAAGAAA[C/T]GAGAGATTAAGGTTG | 23092 |
| rs11744705 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134728 | GTTCTTTGCAATGAT[C/G]AGGTACTGACCCCTA | 23092 |
| rs11745299 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963200 | tatatatatatatat[A/G]tgtgtgtgtgtgtgt | 23092 |
| rs11746282 | snp | C/T | 0.100231 | 0.200173 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780722 | TATCTTTGTGCGGTG[C/T]GTGTAACATTCAGGA | 23092 |
| rs11746557 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829253 | TGACCAAATGTCCTA[A/G]GTCACACCTGCTATC | 23092 |
| rs11747151 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088063 | tgggatgtggcactt[C/T]taaaaggtctcacat | 23092 |
| rs11747798 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180323 | tagagacggggtttc[A/C]ccatgttggccagga | 23092 |
| rs11748220 | snp | A/G | 0.109814 | 0.206997 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172365 | ATTAACAAAGGCTGA[A/G]AGAGGAAGAGAGTAA | 23092 |
| rs11749472 | snp | C/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972624 | agacagattaacata[C/G]tgatcatctcacagt | 23092 |
| rs11749540 | snp | G/T | 0.182296 | 0.240658 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780302 | CCATTGCAAGTAATG[G/T]TGTTGTGAACATCCT | 23092 |
| rs11749756 | snp | C/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185953 | TCCTAAAGGAGCCAT[C/G]CTATTTAAAGAGCCA | 23092 |
| rs11750326 | snp | A/C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141767 | CTGTCTTGTGAGTAA[A/C/T]ACAGTGTCCATTTAA | 23092 |
| rs11750569 | snp | C/T | 0.123798 | 0.215808 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082451 | AATAATAAAATTAGT[C/T]TGAATTTGTTGAAAA | 23092 |
| rs11750827 | snp | C/T | 0.468349 | 0.121752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006506 | CCATCAACTATATTT[C/T]TATTGGTTTCACATT | 23092 |
| rs11948197 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016783 | GGTATTGATTGATTT[A/C]TAAGCTGGCAAACCA | 23092 |
| rs11950522 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987699 | tattgagagttttta[A/G]catgaagagctgttg | 23092 |
| rs11950635 | snp | G/T | 0.0715223 | 0.175059 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120542 | AAAATTATGTCTATT[G/T]AATGCTTATGTTTGC | 23092 |
| rs11950750 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885104 | CTGGTCTTGTCCTGG[G/T]TGGTGCCTCTCTGCT | 23092 |
| rs11951301 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812632 | catgagccaccacgc[A/G]cagcttcaatcctcc | 23092 |
| rs11951777 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217437 | GGAAAGAGAAATAGC[A/T]CATATTCTCAGGAAC | 23092 |
| rs11952702 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093155 | ctttttgcttttttt[A/T]tttttggacttaggg | 23092 |
| rs11954679 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946698 | GTTGTTTGCTTTGTG[A/G]TGAGGTGTGAAACAG | 23092 |
| rs11955858 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094148 | tcccgactaaggaat[A/G]ctttaccgcccctgc | 23092 |
| rs11956057 | snp | C/T | 0.26271 | 0.249677 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036424 | TTTCTGGGTGAGAAT[C/T]CTGTCACCACTTGCT | 23092 |
| rs11956059 | snp | C/T | 0.262159 | 0.249704 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036440 | CTGTCACCACTTGCT[C/T]ATTTCCCCCTAGAGG | 23092 |
| rs11956107 | snp | C/G | 0.455926 | 0.141755 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868841 | ATCCATGTCTCAGCT[C/G]TCTGTCATGGGTCCT | 23092 |
| rs11956297 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826157 | GAGGGGGATATGATA[C/T]GTGATCAAATTGTCT | 23092 |
| rs11956857 | snp | G/T | 0.107341 | 0.205301 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030300 | CTTGACCCTCATTTA[G/T]ATGGCCGAGTTAGTG | 23092 |
| rs11959109 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801698 | CCCACCCCTCCCCCA[A/G]CCCCCGCCTTTGGCT | 23092 |
| rs11960127 | snp | A/G | 0.441295 | 0.160954 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103913 | cagcacattctgcac[A/G]tgtatcccagaactt | 23092 |
| rs11960157 | snp | A/G | 0.264632 | 0.249571 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039046 | GCTCAGTATGAGCCC[A/G]TTCTGGGAGCAGTGG | 23092 |
| rs11960805 | snp | C/T | 0.105569 | 0.204058 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036550 | TCTTCTTTTATTCTT[C/T]GTTCTATTTTTCCTT | 23092 |
| rs12108818 | snp | C/G | 0.264906 | 0.249555 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163699 | ctggtgatccatcca[C/G]ctcggtctcccaaag | 23092 |
| rs12108933 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144719 | ggctCATTTTCTCCT[C/T]ATTTCCTAATTGACT | 23092 |
| rs12108936 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144880 | TCAGCCTTTTGGCTT[C/T]GATCTTCTACCTAGA | 23092 |
| rs12109255 | snp | C/T | 0.213333 | 0.247296 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786671 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTGAGATGG | 23092 |
| rs12109590 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205795 | TTTGTGGGCTTGTTG[C/T]GTGGGTAAATGAGAC | 23092 |
| rs12109619 | snp | C/G | 0.264358 | 0.249587 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163824 | CTCAGACCCTACCAA[C/G]CTATGTCCCCAATTT | 23092 |
| rs12109718 | snp | G/T | 0.324382 | 0.238678 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194661 | TATTTGGTTTTGAAG[G/T]ACAAGAACTAGAAGA | 23092 |
| rs12110264 | snp | A/G | 0.103082 | 0.202275 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142871 | TAACAAGTAGGAGAA[A/G]GTACACCTCTCTCCT | 23092 |
| rs12153264 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833644 | ttgGGGACATCCTAC[C/T]TACCGCTGATATTTG | 23092 |
| rs12186402 | snp | C/T | 0.346147 | 0.230772 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192585 | tatttactttatggc[C/T]ccttaagaaaaagtt | 23092 |
| rs12187464 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922411 | TACACCTTGTATACA[C/T]TGACAGAAGAgtgtg | 23092 |
| rs12187598 | snp | C/T | 0.49949 | 0.0159663 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023104 | GGGTCAGACCCTTAG[C/T]GTGGCCCACCACTCT | 23092 |
| rs12188243 | snp | C/T | 0.412249 | 0.190198 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026195 | TCGGCTCCTTGTGTT[C/T]TCAGCTGGTGAAAAC | 23092 |
| rs12189299 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076969 | caaacatccttttgc[A/T]catgtgtgagtttta | 23092 |
| rs12234019 | snp | A/G | 0.398894 | 0.200825 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201799 | GACATGCATCTTTGC[A/G]GTACATAAAATGTGC | 23092 |
| rs12332305 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046500 | TCATAGCAAGTGCAG[C/T]GTGGCTTTGTACTAG | 23092 |
| rs12332695 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138279 | ATAAGACAGCAAGTC[A/G]CTCCTCATATCATAG | 23092 |
| rs12374576 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950221 | TGGGGAGGGGCAGGA[C/T]AGGCAGAAAGCTGAA | 23092 |
| rs12513442 | snp | A/T | 0.452842 | 0.146134 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858096 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 23092 |
| rs12513586 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118448 | AGGAAAGGTATGCTG[A/T]TTTATAAGAGTTCAG | 23092 |
| rs12513965 | snp | C/T | 0.404907 | 0.196224 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857921 | TAAAAAGGCATACTT[C/T]CAGATGTATTTTCCA | 23092 |
| rs12513994 | snp | A/T | 0.330249 | 0.23677 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858094 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 23092 |
| rs12514082 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918854 | AAACTTGCTTGGATC[A/G]AGGTATCATGTCAGT | 23092 |
| rs12514104 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081268 | gctctacagcattta[G/T]aagtgggaagaggag | 23092 |
| rs12514539 | snp | C/T | 0.462909 | 0.131034 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989422 | gatgggtcttgactc[C/T]ttatccagtttgcaa | 23092 |
| rs12517199 | snp | G/T | 0.103438 | 0.202533 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859723 | tgctccaccttcagc[G/T]tacgatgtgtgagga | 23092 |
| rs12517479 | snp | A/G | 0.180383 | 0.240111 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820277 | TTAGGATTGTTGTGC[A/G]GTGGTTAAAACTTTC | 23092 |
| rs12517748 | snp | A/G | 0.498693 | 0.0255257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991191 | cccagccttgctgcc[A/G]ccttgcagttcgatc | 23092 |
| rs12517878 | snp | C/T | 0.344815 | 0.231323 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853341 | GACTGCAGGCATGTG[C/T]CACCACATCCAGCTA | 23092 |
| rs12518131 | snp | C/T | 0.410568 | 0.191619 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039352 | AACTGGCATTACAGG[C/T]GCCTGCCACCATGCC | 23092 |
| rs12518512 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955310 | tgtctcaaaaaaaaa[A/T]TTTTTTTTTAAAGCC | 23092 |
| rs12518688 | snp | C/T | 0.480697 | 0.0963277 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039510 | CTGTGCACGGTCTAA[C/T]TTTCAACAGGAGTTT | 23092 |
| rs12519015 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123344 | TTCAGGCCTAGCCTG[A/G]TATGAAGTAAGGAGA | 23092 |
| rs12519983 | snp | A/G | 0.0998734 | 0.199905 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869137 | CCAATCCTGTTGCAA[A/G]TTCTAACCTCAATGA | 23092 |
| rs12520023 | snp | C/T | 0.182933 | 0.240836 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796005 | TTTCTATAGTACTTA[C/T]CTTGTTTTAACATGC | 23092 |
| rs12520307 | snp | A/G | 0.461259 | 0.133677 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094681 | tcttatccctgacac[A/G]tgtggcccctgctgc | 23092 |
| rs12520828 | snp | A/G | 0.392325 | 0.205532 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864712 | AGCAAGGCAGGGCCG[A/G]GGGCATCCCTGTCCT | 23092 |
| rs12522327 | snp | C/G | 0.432944 | 0.170387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990355 | tagttagctatttgt[C/G]taatcttttttcaag | 23092 |
| rs12522841 | snp | A/G | 0.380724 | 0.213099 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139110 | AGCTGGGCATCTGCC[A/G]GTAAAATGCTGAGGG | 23092 |
| rs12523120 | snp | C/G | 0.143959 | 0.226396 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803426 | TTCAAATAGGATGCA[C/G]AGGTATGATTTTATT | 23092 |
| rs12523539 | snp | A/T | 0.411914 | 0.190483 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036543 | TCATTTTTCTTCTTT[A/T]ATTCTTTGTTCTATT | 23092 |
| rs12653185 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820462 | AAAAAAACAAACAAA[A/C]AAAACCCACCTAAGG | 23092 |
| rs12654050 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114104 | AGGAGACACTGTGTA[A/G]AAGTACCCACCATAA | 23092 |
| rs12654456 | snp | A/G | 0.3744 | 0.216852 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022673 | GTTTTGAGAGGGAGC[A/G]TGAAAGTGTCACACG | 23092 |
| rs12654475 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897653 | CAAAGGAAGAACATG[A/G]AATAACAATTGATGA | 23092 |
| rs12655791 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225622 | TTTGGCCCCAGCTTC[A/C]CTGCTTGGAAGCATG | 23092 |
| rs12655882 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925348 | GCAAAAGAAAAAACC[A/T]AGAGCAACATAAGAC | 23092 |
| rs12656904 | snp | C/T | 0.214239 | 0.247429 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071745 | aaaccccatctctac[C/T]acaaaaaaattagcc | 23092 |
| rs12657060 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176722 | GGGCTTAACGTAAAC[C/T]TAAGTAGCAGACCAT | 23092 |
| rs12657072 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081785 | CTGGGAGGCCGAGGC[C/T]GGCGGATCACAAGGT | 23092 |
| rs12657977 | snp | C/G | 0.123452 | 0.215605 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888315 | GGATGTTGAGGCTCT[C/G]TTGCCTGCTGACCAT | 23092 |
| rs12658072 | snp | C/T | 0.236724 | 0.249647 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833084 | TTTTGAGGTGGAGTT[C/T]CACTTTTGTTGCCCA | 23092 |
| rs12658588 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160183 | tcctgcctcagcctc[C/T]tgaatagctgggact | 23092 |
| rs12658615 | snp | C/T | 0.215446 | 0.2476 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883608 | AGCTTGTTAGGGCTC[C/T]GGGTGATGGCTTCTG | 23092 |
| rs12659189 | snp | C/G | 0.122411 | 0.214991 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860474 | TGGCTCTCCAGCTGC[C/G]TCTTCTGTGGGAAGC | 23092 |
| rs12659987 | snp | C/G | 0.0908922 | 0.192833 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815764 | ACTTTCCCCGGCTAG[C/G]CTTCCTGGTCCATCT | 23092 |
| rs13153145 | snp | A/G | 0.176413 | 0.242186 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861571 | GAGGAGGGCGAGAGG[A/G]AGTCAAAGTGGTAGG | 23092 |
| rs13153374 | snp | A/T | 0.159292 | 0.232964 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854687 | CCTAGGATCTGAATT[A/T]CTTTAACTTCGTTAC | 23092 |
| rs13153983 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128059 | CCTTGTTAGGGTTCA[A/G]AAGCAAGCTAGATTT | 23092 |
| rs13154796 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994953 | atttaataaatggtg[C/T]tgggaaaactggcta | 23092 |
| rs13154804 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034735 | aaacttatggtatat[C/G]aagtatataccaaga | 23092 |
| rs13155105 | snp | A/G | 0.105569 | 0.204058 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034933 | GCCATAATTTGCAGA[A/G]CAAATACTTTATTTA | 23092 |
| rs13155258 | snp | A/C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128118 | CCACAGGGCTATTTT[A/C/T]TTTTTTTAGTGACAA | 23092 |
| rs13155844 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988359 | tatcattttttattg[G/T]ttctagtttattctt | 23092 |
| rs13157165 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948356 | atatgtgtgcatatg[A/T]gaatatgtatatata | 23092 |
| rs13157734 | snp | A/G | 0.0452528 | 0.143452 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963202 | tatatatatatatgt[A/G]tgtgtgtgtgtgtgt | 23092 |
| rs13158233 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168539 | CACAAGATCTTACGA[C/T]ATTCTGCATCATCCT | 23092 |
| rs13158374 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168634 | TCTTCTGTGTTGCAA[A/C]CCAAGACTAAGCACA | 23092 |
| rs13158961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805189 | ctcactgcaacctcc[A/G]cctctcgggttcaag | 23092 |
| rs13159551 | snp | C/T | 0.159951 | 0.233219 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862574 | GTCTTTTGATAACTC[C/T]CTGGTAGAAGTGGTG | 23092 |
| rs13159761 | snp | A/G | 0.26271 | 0.249677 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035532 | atggactttggggac[A/G]tgggggaaaggatgg | 23092 |
| rs13159941 | snp | A/G | 0.105214 | 0.203807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184983 | attaatgagaggtct[A/G]tgcaacagtgagtgg | 23092 |
| rs13160342 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097388 | aaaaaaaaaAAGAGC[A/T]TATCTGACTGTAAAG | 23092 |
| rs13160714 | snp | C/T | | | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143069058 | tgctATGCCCCAGGA[C/T]TCTGTCCTTCAGGCC | 23092 |
| rs13160715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143069060 | ctATGCCCCAGGACT[C/T]TGTCCTTCAGGCCTC | 23092 |
| rs13160845 | snp | C/T | | | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143069103 | CCCTCCTGCCATCCT[C/T]TCTCCTTCCCAATGA | 23092 |
| rs13160847 | snp | C/T | | | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143069105 | CTCCTGCCATCCTCT[C/T]Tccttcccaatgagg | 23092 |
| rs13161500 | snp | A/G | 0.234692 | 0.249531 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999296 | CTGAAAATTAGCCTC[A/G]AGCATATAGATCTTT | 23092 |
| rs13162212 | snp | A/G | 0.486266 | 0.0817214 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997448 | gggttttgctctgtc[A/G]cccaggctggagggc | 23092 |
| rs13162227 | snp | C/T | 0.26271 | 0.249677 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036333 | TAGGGAATTTCCAGC[C/T]TTGTTGTCAGGTTAG | 23092 |
| rs13162252 | snp | C/G | 0.107341 | 0.205301 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023841 | GAGGACAGACACTCT[C/G]CCTCCCTCCCTTGCC | 23092 |
| rs13163572 | snp | C/T | 0.193028 | 0.243422 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875962 | TACCCAGGCTGATCT[C/T]GAACTCCAAACCTTA | 23092 |
| rs13163604 | snp | A/G | 0.274393 | 0.248807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038093 | CCGCTGAGAAAAGCT[A/G]TTAACCATCTTTCCA | 23092 |
| rs13163960 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103291 | tttaaaagtcaggaa[A/G]caacagatgctggag | 23092 |
| rs13164093 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103305 | aacaacagatgctgg[A/T]gaggatgtggagaaa | 23092 |
| rs13164444 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869208 | TTCTTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs13164564 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217844 | CTTCTTCACATAGCA[A/G]CAAGAGTCATCTTTG | 23092 |
| rs13164657 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130092 | CGTGTAGCTGTAGGT[A/G]TTGCTGCCCACTGAA | 23092 |
| rs13165485 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908067 | CATATATACAATATC[A/G]AGCGTATCAAATATT | 23092 |
| rs13165650 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057275 | ATTTGTTTATCACTT[C/T]ACAAGTGCATAAAGT | 23092 |
| rs13166709 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044609 | GGGGTGGGGACGGGG[G/T]TAGTCCCTGAAACCC | 23092 |
| rs13167638 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929796 | GCCCCTGAGACCTTG[A/G]TATGTAGACAGCTCT | 23092 |
| rs13167916 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103168 | CTTCTTTACCTGTTC[C/T]TTTGATTTGCTTTGC | 23092 |
| rs13167928 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103197 | GCTGCAGACTAATTG[G/T]GCCTGGGACCTTAAA | 23092 |
| rs13167954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794411 | GCAACGCAGTTACTC[C/T]ACACTGGCATAAGTA | 23092 |
| rs13169129 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012519 | AGAGTAGCCATTAGA[A/G/T]TCACTGGAGGGatat | 23092 |
| rs13169445 | snp | A/G | 0.339203 | 0.233544 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192155 | CAATGTAGCATCAAG[A/G]CGGGAAGAAAAACAC | 23092 |
| rs13169865 | snp | A/G | 0.266819 | 0.249434 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925125 | TGATCATGCCTTCCC[A/G]CATGCCAGCTACCGG | 23092 |
| rs13170271 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012548 | atatttatatacata[C/T]atacatatatatata | 23092 |
| rs13170546 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973812 | AAGTAGGTCAGCAAC[A/C]CAACCAGAAAAAGAC | 23092 |
| rs13170806 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886205 | TATGTTTGCCAAAAG[A/T]GGCTACCGTGGCTTC | 23092 |
| rs13172530 | snp | C/T | 0.454664 | 0.143571 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985846 | ccaactcatcctttt[C/T]tatggctgcatagta | 23092 |
| rs13172596 | snp | C/G | 0.193653 | 0.243567 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855303 | GTTTACAGAGGAGGT[C/G]GAATACCAGATGCAT | 23092 |
| rs13172701 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816424 | GGTATCATAGAGAAC[A/C]CAATTAAATAGTGCC | 23092 |
| rs13172733 | snp | A/G | 0.463774 | 0.129618 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992115 | TTTTCTCCTTTTGCA[A/G]TTAGTTTATCCTTTG | 23092 |
| rs13174511 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128060 | CTTGTTAGGGTTCAG[A/G]AGCAAGCTAGATTTA | 23092 |
| rs13174527 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128091 | CTTGGGTGTTGAGCT[A/C]GAATGCTTCTGCCAC | 23092 |
| rs13174827 | snp | G/T | 0.105924 | 0.204309 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034249 | tgccactcctaggtg[G/T]atactcaaaagaaat | 23092 |
| rs13175350 | snp | C/T | 0.462909 | 0.131034 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210236 | GAGGAGGAAGTCACG[C/T]CTTTCATGGATGGCG | 23092 |
| rs13175463 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014248 | TTCCCGAGTGCAGTG[A/G]GACATGCCTCCACCC | 23092 |
| rs13175511 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800596 | tctaactcctgacct[C/T]aggtgatccacccac | 23092 |
| rs13176749 | snp | A/G | 0.364193 | 0.222396 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883883 | TAGAACATTTCTACC[A/G]TGAGGGTTGGGACCA | 23092 |
| rs13177971 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168679 | ACACCTTCAGCTTTT[A/T]GCAAAGGCTGTTTGG | 23092 |
| rs13178831 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128099 | TTGAGCTAGAATGCT[C/T]CTGCCACAGGGCTAT | 23092 |
| rs13179648 | snp | A/G | 0.353587 | 0.22753 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193885 | AAACATAGTATATAC[A/G]TAGTTTGGTACTATC | 23092 |
| rs13179771 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173305 | cctcccaaagcacta[G/T]gattacgagcatgag | 23092 |
| rs13179954 | snp | A/T | 0.350982 | 0.228698 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194049 | CCTGCCCTGCAGTGA[A/T]ATCAGCAGGACACTG | 23092 |
| rs13180681 | snp | G/T | 0.263809 | 0.249618 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037980 | AGATCAAGGAGGCTG[G/T]TTCATCCTGATGGTC | 23092 |
| rs13181197 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103270 | ACTCTTCAAAGAAAT[A/G]AAACTtttaaaagtc | 23092 |
| rs13181333 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103304 | aaacaacagatgctg[C/G]agaggatgtggagaa | 23092 |
| rs13181851 | snp | A/G | 0.173965 | 0.238157 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789598 | TAAGTATCTGTTGTA[A/G]TACTTAACAAAAAGT | 23092 |
| rs13181982 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168606 | AAATAGGTTCAAAAA[C/T]AAGCTGTATTCCTCT | 23092 |
| rs13182153 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832368 | ataaaaagagacaac[C/T]gagagcaggctctct | 23092 |
| rs13182178 | snp | C/T | 0.274393 | 0.248807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038109 | TTAACCATCTTTCCA[C/T]TGGATTTGATTTGAA | 23092 |
| rs13182241 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103167 | TCTTCTTTACCTGTT[A/C]TTTTGATTTGCTTTG | 23092 |
| rs13182415 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103292 | ttaaaagtcaggaaa[A/C]aacagatgctggaga | 23092 |
| rs13183774 | snp | C/T | 0.35207 | 0.228214 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193891 | AGTATATACATAGTT[C/T]GGTACTATCCACGGT | 23092 |
| rs13183877 | snp | A/G | 0.031825 | 0.122064 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929331 | ACATGAATTAAATTG[A/G]CATCCTGTAAGAGAA | 23092 |
| rs13184088 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850414 | CTGCTTTTTCTTTTT[C/T]TTGCAACCAGCATTA | 23092 |
| rs13185255 | snp | A/G | 0.391769 | 0.205917 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864010 | CCCCACCATTCTTAG[A/G]CCTCTATCTCCCTCT | 23092 |
| rs13185496 | snp | C/T | 0.447291 | 0.153545 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108863 | CTGCAATGAGATTTA[C/T]ATCTCTTGGGAAGTG | 23092 |
| rs13186446 | snp | G/T | 0.234692 | 0.249531 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951325 | TCGACCTCCCAAAGT[G/T]CTGGGATTACAGGCA | 23092 |
| rs13186593 | snp | A/G | 0.400147 | 0.19989 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094794 | gagtggtttgggggg[A/G]aaatggctatgacag | 23092 |
| rs13186660 | snp | A/G | 0.0962929 | 0.197165 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192178 | AAAAACACAGCCCTT[A/G]AAGATTCCAAGGAGA | 23092 |
| rs13186673 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009249 | CAAGTTCTTCCTTCC[A/G]GTGATTCACCTGCCC | 23092 |
| rs13186856 | snp | C/T | 0.212728 | 0.247206 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038764 | gcagtaatgcagtct[C/T]ggttcactgcaaact | 23092 |
| rs13186877 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861336 | GTGTGGCTTTGTTCA[A/G]AATGGCTAGGTCCGT | 23092 |
| rs13187932 | snp | A/G | 0.229429 | 0.249152 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908980 | TTATTTTCTTCCTTT[A/G]ATATTCTACATTTCA | 23092 |
| rs13187956 | snp | A/G | 0.262985 | 0.249663 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034135 | gaaattggaaccctc[A/G]tacattgcgggtagg | 23092 |
| rs13188048 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886206 | ATGTTTGCCAAAAGA[A/G]GCTACCGTGGCTTCC | 23092 |
| rs13188062 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869209 | TCTTTTTCTTTTTTC[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs13188339 | snp | C/T | 0.338976 | 0.23363 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192461 | CCAGGTGCCTGCTTG[C/T]TCTATGGCTTGTGAG | 23092 |
| rs13188405 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938610 | TAGAATTTCTACCAG[C/T]CCATCATCATTGCCA | 23092 |
| rs13188969 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791004 | CCACTTGACTTTTTT[A/C]TAGAAGCAACTCTAA | 23092 |
| rs13189135 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894051 | TATGTATTTAAGTTG[G/T]ATAATATGATGTTTC | 23092 |
| rs13189151 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894084 | TATATTTTTGCATAG[G/T]GAAATAGTTACTATA | 23092 |
| rs13189276 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894115 | GTTATTCTTCTTCTG[G/T]GTAATGCTATTTGAT | 23092 |
| rs13189916 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012616 | TTCTATACCTACAGA[A/C]CCTTAATGACCAAAG | 23092 |
| rs13189966 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012494 | GGGTTAAATAAGTGG[G/T]TCTCAACTGAGAGTA | 23092 |
| rs13328193 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065881 | GAGCTGAGTATCTCA[A/G]AAGCAATTGTTCAAC | 23092 |
| rs13340374 | snp | C/T | 0.143284 | 0.226079 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074821 | gcagctgttatatca[C/T]atgcctacagcatgc | 23092 |
| rs13354474 | snp | C/T | 0.292008 | 0.246445 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928016 | GTTCATTTTTTCTTA[C/T]TCACTTGTAGGCATT | 23092 |
| rs13354582 | snp | C/G | 0.0154538 | 0.0865337 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229458 | CAGGCCAAGCCAGAT[C/G]ACTGAGTCTTCGCAT | 23092 |
| rs13355926 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784783 | atggcttttagtata[C/T]gcacaggattttgca | 23092 |
| rs13356063 | snp | A/G | 0.106633 | 0.204807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118976 | GAAGAAAGAAAAACA[A/G]TGGGGCCCACTACAG | 23092 |
| rs13356911 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098280 | TGTTAAATGGTATTT[A/T]AAAAAGCCAATTCCT | 23092 |
| rs13357476 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785076 | gctgggtctacaggc[A/G]cccaccaccatgccc | 23092 |
| rs13357498 | snp | C/T | 0.351635 | 0.228408 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194205 | ACATTCGTTAAGTAA[C/T]GAGAAATTTATGAGC | 23092 |
| rs13436025 | snp | A/G | 0.20511 | 0.245937 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783962 | CCCCTGCTGTGGACA[A/G]TATGTCATTGTGGAG | 23092 |
| rs13436658 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781961 | acttcgtgatctgcc[C/T]gccttggcctcccag | 23092 |
| rs13436659 | snp | A/C/T | 0.0345262 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782006 | aggcatgagccactg[A/C/T]gcctggccGATTCAT | 23092 |
| rs17096377 | snp | C/T | 0.105924 | 0.204309 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973304 | TGGAGTCCTGTGCAG[C/T]ATTTTCTATGTGATG | 23092 |
| rs17099475 | snp | C/T | 0.461259 | 0.133677 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779034 | TAGCCCTGGAACTGC[C/T]TGATATGCTTTCTGA | 23092 |
| rs17099517 | snp | C/G | 0.45692 | 0.1403 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797801 | CTCCAAAGACCAGTT[C/G]CCACTCTGTTGGGGG | 23092 |
| rs17099520 | snp | A/G | 0.0105817 | 0.0719645 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801789 | AAAGTACCTTGTCTT[A/G]AACTTTTGTGGTTAG | 23092 |
| rs17099585 | snp | A/G | 0.44755 | 0.153212 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825794 | ACTCCAGATCAGAGA[A/G]CAGGAAACTTTTCCT | 23092 |
| rs17099608 | snp | C/T | 0.240765 | 0.249829 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848492 | CTGTGGTCAGATTCT[C/T]ACCATAGGTGGTTCT | 23092 |
| rs17099616 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855172 | AACATAAATGCTCTC[A/C]GTGGTGGAGAAAGAC | 23092 |
| rs17099620 | snp | C/T | 0.264906 | 0.249555 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855813 | GACTGACTTATATAC[C/T]CTCACTTGTAATGCC | 23092 |
| rs17099633 | snp | C/T | 0.100231 | 0.200173 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870340 | CCAATCTTACTGGAT[C/T]GAAATTGGCAAGAAG | 23092 |
| rs17099643 | snp | G/T | 0.130008 | 0.219321 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882998 | AGGTGAAAACCATCT[G/T]GTGTCCTGAGTAATG | 23092 |
| rs17099647 | snp | A/G | 0.248471 | 0.249995 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883414 | AAATTTGAAGGAGTA[A/G]TGTGTCCTCAGGCTT | 23092 |
| rs17099651 | snp | G/T | 0.364193 | 0.222396 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883570 | TGAGCATGTACCAGA[G/T]GAGTGGTATTCTGAC | 23092 |
| rs17099688 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911037 | GATTATTTTCCTTTA[A/G]AAGTACCCACTGTTC | 23092 |
| rs17099693 | snp | A/G | 0.215747 | 0.247642 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911197 | CCCAAAACCGATCCT[A/G]TCCCTTCTTTTGATT | 23092 |
| rs17099698 | snp | C/G | 0.0685596 | 0.171987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914202 | GCCTGGGGTTGCACT[C/G]CCTTCTTCTGGCAGG | 23092 |
| rs17099709 | snp | A/G | 0.290977 | 0.246619 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928343 | CCAGTTATTCTGGAC[A/G]CTATTGAATTCTTGT | 23092 |
| rs17099768 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975906 | TAACAAGAATATAAT[G/T]TGGCCTCTGAACACC | 23092 |
| rs17099770 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982814 | AAGATGGACCAGAAA[C/T]TGATGTGAGGCCCTG | 23092 |
| rs17099779 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994239 | ATTGAAGGATGTTCA[C/T]GGGCAGAGATGCATA | 23092 |
| rs17099782 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998399 | TTGTGCGTTCATCTG[C/T]CATGCTCTCAAGACA | 23092 |
| rs17099783 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999523 | GTGAGTTTCAAATCT[A/G]GGTTATGACTCAGAA | 23092 |
| rs17099784 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002204 | GACTCACTCTCTGCC[C/T]GTTGTTTCTCCTGGG | 23092 |
| rs17099823 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049901 | CTCATGTTTCTTCTA[C/T]GGCTCTCCTTCTGAT | 23092 |
| rs17099836 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052868 | GAACAGCTTTCTTCA[C/T]TGATGTCCCAGAATT | 23092 |
| rs17099850 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073514 | GGCACTGACTTATCT[A/G]TGAGGCTAATTATTT | 23092 |
| rs17099857 | snp | A/G | 0.103794 | 0.20279 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077212 | TATTTCCCATTTACC[A/G]TGAACTGTAAAAGAG | 23092 |
| rs17099858 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083926 | AAGTCATTATATTAC[C/G]TGTCATAAAAATTAA | 23092 |
| rs17099984 | snp | A/G | 0.223225 | 0.248562 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110438 | GTAGAAAGTCCCAAA[A/G]CAATGTCTCCATGGC | 23092 |
| rs17100033 | snp | A/G | 0.225301 | 0.248777 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128997 | AAATTGCAGGCGCAT[A/G]TGACAGATGGGATTG | 23092 |
| rs17100039 | snp | C/G | 0.257176 | 0.249897 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139854 | AGGTACTGACACACA[C/G]GCTGTGCTTTTTCTG | 23092 |
| rs17100090 | snp | A/G | 0.260504 | 0.249779 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168056 | CTTTGAACTGGGATG[A/G]TCAAGGAAGGCTTTG | 23092 |
| rs17100104 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173786 | GTTCTGAGTCATGCT[C/G]TGTGGAAGGGAGAGG | 23092 |
| rs17100126 | snp | A/G | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192260 | CTGAGGAAGGAGGTC[A/G]CATTTGAAATGGGCT | 23092 |
| rs17100139 | snp | C/T | 0.103794 | 0.20279 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195376 | TAGTTACTCCTTTGT[C/T]TTCAGCAGTGGACAT | 23092 |
| rs17100142 | snp | A/G | 0.429688 | 0.173817 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197731 | CCTTCAGTTTCTGGA[A/G]TTATTTCTTCTAAAA | 23092 |
| rs17100148 | snp | A/G | 0.107694 | 0.205546 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205089 | AGACTGCACAGTAGA[A/G]AGGAGTTGACACTTT | 23092 |
| rs17100149 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205447 | GATTTTGTTGGAATT[C/T]AGAATATGTTGAGTC | 23092 |
| rs17100157 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214349 | CCACTGTAAATGAGA[C/T]TGTGCCTGCAAAAGA | 23092 |
| rs17100165 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220963 | AAAACAAGCTCAGGA[A/G]GTCATTTAATTAGCC | 23092 |
| rs17100167 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222057 | GAGCTTCAGAAAATC[C/T]GTGAAACCCCTAAAA | 23092 |
| rs17100171 | snp | C/T | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224196 | TATTCTTTAAGTTAG[C/T]TGCTCACACACTTAG | 23092 |
| rs17100180 | snp | A/G | 0.029116 | 0.117091 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226885 | CCAAGGCACTTGCCC[A/G]GAGCTGCAGAGTTGT | 23092 |
| rs17100182 | snp | C/T | 0.0174175 | 0.0916809 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227325 | GCCAAAGGAGTTATC[C/T]ATCATCTCTGGCAAA | 23092 |
| rs17208943 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877553 | ACCATCTGCAATTGC[C/T]CATTTGACAGATGAG | 23092 |
| rs17208950 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883160 | TCTTAAACATGGAAT[A/G]TGGAGGCACAAGTTG | 23092 |
| rs17208964 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898398 | AATTGAAGGTTGGCT[A/C]GTGCCCCAGAGAACT | 23092 |
| rs17208999 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915929 | AGACTCCTGTACTTT[C/T]CTTTTTCACCAATGT | 23092 |
| rs17209076 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113082 | AGAACAGTCAGAAGC[C/T]TTTGGTAGATTTTAA | 23092 |
| rs17209132 | snp | C/T | 0.115438 | 0.210697 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167936 | TGAGTTACAGGGGAT[C/T]GTGCCCTTCACGATG | 23092 |
| rs17209139 | snp | C/T | 0.108755 | 0.206276 | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143172961 | CTTGTCTCCATAGGG[C/T]TCATGCGAGTTCAGC | 23092 |
| rs17209167 | snp | C/G | 0.194902 | 0.243853 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194295 | AGGTGTTTGTACTTA[C/G]AGTGCACAGTAGGAT | 23092 |
| rs17287483 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901102 | ATGTAAGCTCCGAGA[A/G]GAAAGACCACAGGAA | 23092 |
| rs17287545 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944986 | ACAGAGGGTGTGGCA[A/G]CCAAATGTGCACTCC | 23092 |
| rs17287559 | snp | A/G | 0.0622301 | 0.165053 | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961614 | ACCTGACCTATGGGT[A/G]TTACTGGCTATGAAT | 23092 |
| rs17287593 | snp | C/T | 0.14933 | 0.228835 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121863 | GCTTCTCAGAACTTG[C/T]GCAGGGTTCCCTAAA | 23092 |
| rs17287613 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145662 | TTTCTCTTTGTTGTC[A/G]TTTCTGTTCAAAAAC | 23092 |
| rs17287627 | snp | C/G | 0.211516 | 0.24702 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152489 | TGAAACTTGGGAGCA[C/G]ATGATACTCTCTGGT | 23092 |
| rs17287634 | snp | A/T | 0.102726 | 0.202016 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153924 | CTGGAATTCAAAGGA[A/T]AAACAAGGCCTGCGT | 23092 |
| rs17287641 | snp | A/G | 0.205417 | 0.245993 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164590 | AGCAGCTCTTCTTCC[A/G]CCTCCAGGAGTTTAT | 23092 |
| rs17287647 | snp | A/G | 0.186421 | 0.24178 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175606 | TAAACAGCCCTTCTC[A/G]GTTGGTACAGACTTC | 23092 |
| rs17541029 | snp | C/T | 0.412416 | 0.190055 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025456 | CTCTGTTTGAAACAC[C/T]TCCACCCTCAGAAAG | 23092 |
| rs17541386 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069414 | GGTAGCCCTTTTCAA[A/G]CACTACCTTTATGAT | 23092 |
| rs17541441 | snp | C/T | 0.284733 | 0.247575 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074907 | GGAGGGAGGAGCTCA[C/T]AGCCTAGAGGGTAGC | 23092 |
| rs17541504 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086155 | ATGATAAGAAAAATG[A/T]TGGAAGAATGTTTTT | 23092 |
| rs17613566 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088073 | CACTTCTAAAAGGTC[C/T]CACATAAAGCTGGTG | 23092 |
| rs17650464 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023408 | AGGCTTGAAAACTGT[A/G]GGGAAAGCCTTGATG | 23092 |
| rs17650511 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031122 | GGAGAAAGCATGGTT[A/G]GTTGAATGTTCTTGA | 23092 |
| rs17650523 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031555 | TTTGTTATAATTTTC[C/T]GACCACCTACACACC | 23092 |
| rs17650659 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056531 | CATTTATATAACTTC[A/G]CAGTCCTCTTTTCCA | 23092 |
| rs17650820 | snp | C/T | 0.273856 | 0.248859 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075397 | AATAGACTTTTAGGT[C/T]AAAATAGCAATTTTC | 23092 |
| rs17706955 | snp | C/T | 0.274393 | 0.248807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024789 | ACTGATCAGAGTTGT[C/T]AGAGCCTGCAGCTCA | 23092 |
| rs17707048 | snp | A/G | 0.1652 | 0.235179 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037929 | CAGGCCCATGTTCAC[A/G]CTGATCTTTCCCAGG | 23092 |
| rs17707117 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056572 | CATTTACAGCTTCTG[A/G]TCATTCTTCAACTAC | 23092 |
| rs17707291 | snp | C/T | 0.275197 | 0.248727 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084103 | TGGTCAAAACTATAA[C/T]TGAGTGGGAATTTAA | 23092 |
| rs17707332 | snp | A/C | 0.295343 | 0.245854 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094007 | CCATGGGGATTTCTC[A/C]CCTGTTTTTGAGATT | 23092 |
| rs28369449 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796357 | ATCTCTTAGGACCGT[A/G]GTTCTCTTATCTTTA | 23092 |
| rs28376507 | snp | C/T | 0.216649 | 0.247765 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768558 | CAAGCCTTTGGCTTC[C/T]CTAAATTTCTAACCC | 23092 |
| rs28376515 | snp | A/G | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224826 | GGTATAGATTGTGCC[A/G]TCATAGCTTTACAGG | 23092 |
| rs28422940 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820944 | TGTCCCTCCACCTCC[A/G]CTAGAAATCAAATTA | 23092 |
| rs28523610 | snp | A/G | 0.257454 | 0.249889 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918976 | AAATAAATGTAACTT[A/G]TAGTAGTTGTGTGGT | 23092 |
| rs28576687 | snp | A/C | 0.0170251 | 0.090679 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768505 | CATCCACTCCTCCAG[A/C]TCCTGTCACCATCCA | 23092 |
| rs28593769 | snp | C/T | 0.00301129 | 0.0386856 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222333 | AATGCCATCTCTTCT[C/T]GCTTTCTCTCCCCTT | 23092 |
| rs28617582 | snp | G/T | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142770165 | CGGGGTCTGCAACGC[G/T]GGGAGGGCAAGAGGA | 23092 |
| rs28626979 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123982 | ACACACACACACACA[A/C]AAACACACAATGTCT | 23092 |
| rs28657831 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963198 | TATATATATATATAT[A/G]TGTGTGTGTGTGTGT | 23092 |
| rs28657913 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216913 | ATGCTTACACAGACC[C/G]TCTTCCTCCCCACTC | 23092 |
| rs28670416 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176120 | CTGTGTCTCAAATAA[A/G]TAAATAAATAAATAA | 23092 |
| rs28685829 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956422 | CTCTACTAAAAATTT[A/T]AAAAATTAGCCAAGT | 23092 |
| rs28688005 | snp | C/T | 0.106633 | 0.204807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104660 | ATAAAATATTGGAAA[C/T]AATCTGACTGTCCAA | 23092 |
| rs28700591 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872660 | GACTTTTTAATGATA[A/G]GGGCTCTTGAGAGTT | 23092 |
| rs28702714 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214906 | AAGCACTGTCCTTAA[A/G]CCTTTGCTCCATTAA | 23092 |
| rs28719071 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821189 | GGACCAAGAGAAGAG[C/T]GGGTGAATTACTCAC | 23092 |
| rs33921825 | in-del | -/C | 0.423257 | 0.180228 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163532 | CTTGGCTCACTGCAA[-/C]CTTTGCCTCCTGGGT | 23092 |
| rs33932686 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167518 | AAAAAAAAAAAAAAA[-/A]GAAATCCATTGTTTG | 23092 |
| rs33954372 | in-del | -/C | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226325 | TCTCTACTAAAAATA[-/C]AAAAAATTAGCCGGG | 23092 |
| rs33977810 | in-del | -/C/CAAA | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820461 | AAAAAAACAAACAAA[-/C/CAAA]AAAAACCCACCTAAG | 23092 |
| rs33982471 | in-del | -/GT/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922423 | CATTGACAGAAGAGT[-/GT/TG]GTGTGTGTGTGTGTG | 23092 |
| rs33986453 | in-del | -/TTT | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020654 | TTTTTTTTTTTTTTT[-/TTT]GAGATGGAGTCTTGC | 23092 |
| rs34007921 | in-del | -/A/AA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016720 | AAAAAAAAAAAAAAA[-/A/AA]AATTGGCCACTTTTT | 23092 |
| rs34008745 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036650 | CTAGAGCAAGTCTCC[-/C]ATGTATTGGCTCTGC | 23092 |
| rs34027680 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990207 | TTTCATTCATTTGAT[-/A]CTTCAATCACTGATA | 23092 |
| rs34052309 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781196 | ATCGAGCCCAAGGGG[-/G]CAGTGTGGTCACTAA | 23092 |
| rs34052372 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120885 | TTCTGGCTCCTACAG[-/C]ATGAGGAGTCTATAA | 23092 |
| rs34069423 | snp | A/G | 0.101658 | 0.201233 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842629 | TTGATCTAAAAGTGC[A/G]TAGTAGTAGAGCATG | 23092 |
| rs34070136 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218414 | AGCACGTGGTAGGTG[-/G]CTCAGTAAACATTTG | 23092 |
| rs34070305 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043368 | TATTTTTGCTGTTCC[-/C]ATGTATTAATAGTTC | 23092 |
| rs34070437 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944809 | ATACCCATTGTTTTA[C/T]TCAGTTCTGCTTCTA | 23092 |
| rs34079622 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206879 | AGGCTGGTGATAGCA[C/T]GTGGGTGTGGGAACT | 23092 |
| rs34091570 | snp | C/T | 0.0295035 | 0.117819 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222907 | TAGGCACTCTCTCTA[C/T]CCCACCTCTCAGTAC | 23092 |
| rs34092817 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936107 | TAGAAAATCCCAAGG[-/G]AACACACACACACAC | 23092 |
| rs34094030 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880700 | ACGCCACCTGCAGGG[-/G]CTTTTGGGCAACACC | 23092 |
| rs34095184 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171927 | TTTTTTTTTGTTTCC[-/C]TTCCTTTTATTTCTT | 23092 |
| rs34102649 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940210 | CTTTCTTTGTTAAAA[-/A]TAAGTGATTGAAAGA | 23092 |
| rs34104218 | snp | A/G | 0.104149 | 0.203046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835353 | GGTTCTAGATACCCC[A/G]TGTAAGAGAGTATTC | 23092 |
| rs34112524 | in-del | -/G | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007940 | TACATTGCCAACAAG[-/G]ACCAATGCCACAGGG | 23092 |
| rs34114847 | in-del | -/CCTA | 0.306182 | 0.243605 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857640 | TAATTAATGACCCTA[-/CCTA]GCAAACAATGGCTTA | 23092 |
| rs34116635 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996936 | GGCTATGGAACTCTC[A/G]TAATGTACTGCTGGT | 23092 |
| rs34119763 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818658 | AAATGAGGAAAATGA[C/T]ATTACCACCTTCATG | 23092 |
| rs34120826 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096030 | CAAGTGGTAATTTTT[-/T]AAAAAAATTATTACA | 23092 |
| rs34122289 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844069 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 23092 |
| rs34124664 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209470 | TTGGACACCCTTTAG[-/G]AAGCTGCCCTCTTGA | 23092 |
| rs34130538 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027363 | CTTTTTTTTTTTTTT[-/T]AGTAGAGACAGGATT | 23092 |
| rs34131224 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015760 | ATGGAGACCTCCCCC[-/C]TACACCAGCCAGAAG | 23092 |
| rs34147023 | in-del | -/T | 0.420733 | 0.18262 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937799 | AGTCTCAAAAAAAAA[-/T]ATACTTTAATTTTGT | 23092 |
| rs34148027 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831811 | AGCAATTTCTCATGG[-/G]ATTCAACCTTGATGA | 23092 |
| rs34154406 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006338 | TTTTTTTTTTTTTTT[-/T]TAATTGCAGTTTCTC | 23092 |
| rs34164499 | snp | G/T | 0.125182 | 0.216612 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768769 | AAGAACAATTGTTTT[G/T]GGGTTGTAATTATCT | 23092 |
| rs34178998 | snp | A/G | 0.106633 | 0.204807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834167 | AAACTATTTAAATGT[A/G]AGCTTAGCATGTATC | 23092 |
| rs34179083 | in-del | -/TGTG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806474 | TTATAGGCAATGAAA[-/TGTG]TGTGTGTGTGTGTGT | 23092 |
| rs34190521 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207273 | TCCAGCCCTATGCCC[-/C]ACCTCATCCACGTCC | 23092 |
| rs34191523 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815613 | TCTAGCACCTTCCCC[-/C]TGCTTCCTTTGCAGT | 23092 |
| rs34197001 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110558 | ACTTGGTAACACCAG[-/T]ACTGGCATACACATG | 23092 |
| rs34200638 | in-del | -/GT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922442 | TGTGTGTGTGTGTGT[-/GT]TTTCTGTAGAAAAAA | 23092 |
| rs34209932 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821009 | GTAGCTTTTGCTCTG[-/G]CTTAGAGCAGACAGG | 23092 |
| rs34217434 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130793 | TAAACAACAGTCACT[-/T]GGGGAATGATTTTCC | 23092 |
| rs34227125 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132005 | TTCCAGCTGCTCGGG[-/C]AAGTTAGGAGTTTTT | 23092 |
| rs34237669 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179898 | TTACCATGACCTCCC[-/C]TGTCAAACCTCATGA | 23092 |
| rs34240649 | snp | G/T | 0.46875 | 0.121031 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209654 | GGCATGGTGGTGGGC[G/T]CCTGTAATCCCAGCT | 23092 |
| rs34253008 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793742 | CAGATGTGCGCCACC[-/C]ATGCCTAGCTAATTT | 23092 |
| rs34256924 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783784 | GGTGTCACCACCAGG[-/G]AAATTAGTGCTGCTT | 23092 |
| rs34267203 | snp | A/G | 0.202343 | 0.245416 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840935 | GCAGACAGTAAACAC[A/G]TGGAATTTATGTGTT | 23092 |
| rs34270371 | snp | C/T | 0.48 | 0.0979796 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213279 | AACATTCAACGGACA[C/T]GAGAAAAGCAAAAAC | 23092 |
| rs34288815 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091007 | TAAATGCAATAGTTT[-/T]GAGGCAAAATTGACT | 23092 |
| rs34289461 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158166 | TGTTGATTTCTTTCC[-/C]GTGGTGGCAGTGGAT | 23092 |
| rs34295120 | in-del | -/A/AA | 0.498323 | 0.0289051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041741 | AAAAAAAAAAAAAAA[-/A/AA]AGTGCATTTGGCTGG | 23092 |
| rs34312079 | in-del | -/AAAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154161 | GATTTAAAAATATTA[-/AAAAA]AAAAAAAAAAAAGAG | 23092 |
| rs34312216 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055542 | TGTTTATATCATACC[-/C]TAATGTTAGGGGTTC | 23092 |
| rs34318771 | in-del | -/GCTGAACCTGAG | 0.324145 | 0.238752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032268 | TGTACACTGAGCAGA[-/GCTGAACCTGAG]GCTGAGGGAGGGAAG | 23092 |
| rs34338113 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922905 | GGTCTCAATGCCATG[-/C]ACATTTCAGGCAGGA | 23092 |
| rs34348540 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010275 | TTGGAACATCCTTTT[-/T]AGAGGCAAGATAGAA | 23092 |
| rs34362516 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823827 | GCAGTCTTTCCTTAG[-/G]CTACTTCTGTCTACC | 23092 |
| rs34365485 | in-del | -/AATA | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105379 | ATAAATAAATAAATA[-/AATA]TAAAAATAGGTCTAA | 23092 |
| rs34375638 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017471 | TTCATCACACTCCCC[-/C]TGTTCATGGCACATT | 23092 |
| rs34377952 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078681 | AATTTAAACCTGTCC[-/C]TAGAACTTAAATTAT | 23092 |
| rs34379935 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218339 | ATTGCTTGATTGTCC[-/C]TGCCGAGCAAAATCT | 23092 |
| rs34387315 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802246 | CGTTTTCATTTTATT[-/T]CTGAGCATTCTTTAA | 23092 |
| rs34395064 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997597 | TTTTTTTTTTTTTTT[-/T]AGTAGAGACAAGGTC | 23092 |
| rs34404870 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094413 | TTGATTTCTCACCCC[-/C]TGAGGCTGCCACAAG | 23092 |
| rs34419606 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983052 | GCCCGCCACAAGGGG[-/G]TTGCCCTTTGTTGGC | 23092 |
| rs34444242 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975184 | TAGCATCTGCTTCCC[-/C]TTGTGCTGCTAAACG | 23092 |
| rs34447196 | snp | A/G | 0.137187 | 0.223099 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206930 | ATTTGTCGCCAATGT[A/G]CATGATCGAAGAAGC | 23092 |
| rs34448037 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796316 | ACTCTGCCACAAATT[A/G]CCTCTGTCTTTGAGC | 23092 |
| rs34450175 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074599 | TATTGGAACAGAGCC[-/C]ATGCTCATTTATTTA | 23092 |
| rs34452961 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951959 | ATGCTCCCTCCAGGG[-/G]AAGAATCCTTCCTCA | 23092 |
| rs34455030 | snp | A/T | 0.491051 | 0.0662916 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213236 | AATGCTCCCCAGGTG[A/T]TTCGGATGCACAGTG | 23092 |
| rs34459266 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214789 | TCTCCCAGGTCACAC[-/C]TCAACCCTTGGCCTT | 23092 |
| rs34466756 | snp | C/G | 0.102014 | 0.201495 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835902 | AATCATCACAAAACC[C/G]TCTAAGATTAGTTTT | 23092 |
| rs34469762 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993479 | CGGCCCAATTTTTGT[A/G]TTTTTAATAAAGATG | 23092 |
| rs34501737 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952215 | GGGTGAGGACATGGA[-/A]CCTGTCCTTTTGTGG | 23092 |
| rs34527854 | in-del | -/CACA | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123983 | ACACACACACACACA[-/CACA]AACACACAATGTCTA | 23092 |
| rs34531791 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066958 | AAATGCTCTGTGGGG[-/G]TGGTGCACCTGTTTG | 23092 |
| rs34546007 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812398 | GAGGAGTGTAGTGGC[A/G]TAATCTTGGCTCAGT | 23092 |
| rs34554238 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121295 | TGGTAGTGATGGTGG[-/G]TGATGATAATGTAAG | 23092 |
| rs34558632 | in-del | -/C | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964807 | CGGTGGGCTTCTCCC[-/C]TGTGTGCGGCGACGA | 23092 |
| rs34577770 | in-del | -/ACACACACACACAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162285 | CCCAAACACACACAT[-/ACACACACACACAC]ACACACACACACACG | 23092 |
| rs34590976 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189423 | TCCAAATTACACCCA[-/A]CACACCCTCCCCACC | 23092 |
| rs34602049 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007216 | AAAAAAAAAAAAAAA[-/A]GTTCCTAAATTTAGC | 23092 |
| rs34615747 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895411 | ATTTTTGTATTTTTT[-/T]AGTAGAGACGGGGTT | 23092 |
| rs34622152 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805923 | TAGCAATGCTCCCCC[-/C]TTCTAGAGCATCAAT | 23092 |
| rs34633220 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143058229 | CTTTCTATTCCTTAG[-/T]TTCCCCATCTGTCTA | 23092 |
| rs34645093 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779449 | TGTGTGTGTGTGTTT[-/T]CTTTGCCAGATAGAC | 23092 |
| rs34646838 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853645 | ATGAATAATATCTTT[-/T]GAAAGCACTTGGGGG | 23092 |
| rs34655884 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109146 | GGTGGCTATTAGCTG[A/G]GTAGCAGGTAACTCG | 23092 |
| rs34670227 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821069 | AACTCAAGTGGAAGA[A/T]GAGTAAACTATATCT | 23092 |
| rs34683596 | snp | C/T | 0.238749 | 0.249747 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167474 | CATGACAGAGCAAGA[C/T]TCCATCTCAAAAAAA | 23092 |
| rs34688813 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111295 | ACAGGATATGTATTG[G/T]ATCTCTCCCTCTGTC | 23092 |
| rs34695950 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134544 | GGTGGGACCTTGTAC[A/G]GCTTGATCTTTTACT | 23092 |
| rs34698486 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167308 | CCTCATCTCTACTTT[A/T]AAAAAAAAAAAAAAA | 23092 |
| rs34701807 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102472 | AATCTTTTTCCTCCC[-/T]CTAACTCAGAATGCT | 23092 |
| rs34704039 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812942 | CTTTTTTTTTCTTTC[-/T]TTTTTTTTTTTTTGA | 23092 |
| rs34709127 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857411 | GTGGGCCAGCAGCTG[A/C]TAGGATTCCTGTCTC | 23092 |
| rs34710759 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910011 | GTCATTGGGTAGTGA[-/C]AGAGGTTTATGTGAA | 23092 |
| rs34715200 | in-del | -/C | | | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216373 | AATGGCATTAAAGCC[-/C]TTCAGTGGCCTCCCA | 23092 |
| rs34717549 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072060 | ATACAAGGAACTCAA[-/C]ACATCTCAACAGGAA | 23092 |
| rs34719010 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210245 | TCACGTCTTTCATGG[-/C]ATGGCGGCAGGCAAA | 23092 |
| rs34722383 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038545 | CATAAGGATGTTTAC[A/C]CCGTGGTGATGTTAA | 23092 |
| rs34727882 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873946 | ACCATATAAATTCAA[-/A]TTTATAATCTAAAAT | 23092 |
| rs34756959 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170383 | GCTTTGCAAAAGTCT[C/T]CAACTTGTTGTGACA | 23092 |
| rs34758908 | in-del | -/ATTG | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007823 | CTATTTTTATGTTTG[-/ATTG]CTGTTTTAAAAAAGA | 23092 |
| rs34781991 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150151 | CCTCAGCTTGACTCC[-/C]TGAAGTAGCCATCTC | 23092 |
| rs34784897 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144233 | ATCAGTGACTCAGGG[-/G]AAGTCTAGCTATGTT | 23092 |
| rs34793430 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165245 | TCAGGGCCCCTAGGG[-/G]CCCTGCACTGGTTTT | 23092 |
| rs34797589 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008720 | GTGTGAAAGGGAAAA[-/A]GTTAGATTGTTTTGT | 23092 |
| rs34814057 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851398 | GCTGCGCCCAGCCGG[-/G]AAAATACATTTTTGA | 23092 |
| rs34824730 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119410 | AGAGGAGCTGATGTT[-/G]AAAGTAGTGATGTTA | 23092 |
| rs34833108 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206866 | TGCCTCAGAACAAGG[-/G]CTGGTGATAGCACGT | 23092 |
| rs34843524 | in-del | -/AAAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876798 | AAAAAAAAAAAAAAA[-/AAAAA]GGATTTCTTTAAAAC | 23092 |
| rs34846420 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847363 | GAGATGTCTTTTTTT[-/T]TTTTTGAGACGGAGT | 23092 |
| rs34856554 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883396 | TTGCCTGTACCCTCC[-/C]TCAAATTTGAAGGAG | 23092 |
| rs34878312 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827339 | TCTCCTGAACGTGGG[-/G]CTCAGGTCCTGGCTC | 23092 |
| rs34880113 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945315 | AAGAGATGGAAGATG[C/G]CTGCCACTCACTATA | 23092 |
| rs34891094 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917011 | GAGCCTGTTCCAGGG[-/G]CACATTGGTGCCTCA | 23092 |
| rs34897624 | in-del | -/AA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958931 | AAGAAAAGAAAAAAA[-/AA]GAAAGGAAAATATAT | 23092 |
| rs34897725 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031064 | AGGGTAATGTGAGTT[-/T]GGGAGCCAAAGGCTC | 23092 |
| rs34906170 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974733 | ATACTGAAAGTATTT[-/T]GGCAAGCTGAGCTTC | 23092 |
| rs34907127 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224114 | ATCTTTTACTTTTTT[-/T]TTTTTTGAAAAGATA | 23092 |
| rs34920794 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942654 | CTCACTTCTTCATTT[-/G]CTTTGCAAATATATT | 23092 |
| rs34955772 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114698 | ACCCCAGCACCTGCC[-/C]TGTGTTCTGCAGAAG | 23092 |
| rs34957587 | in-del | -/G | | | intron-variant, frameshift-variant | ARHGAP26 | GRCh38.p7 | 5:143166038 | CAGGCACTGGGGATT[-/G]TGGAATGTGTTTGGA | 23092 |
| rs34964714 | in-del | -/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869384 | GGCTATTTTATTTTA[-/T]TTTTTTTTGTATTTT | 23092 |
| rs34965826 | in-del | -/CTTA | 0.203267 | 0.245593 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880721 | GGGCAACACCACCCT[-/CTTA]CTTTGTGTGGATTTT | 23092 |
| rs34972684 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131821 | ATAGTAGCCATTTTT[-/T]AAATGTCAATGATAA | 23092 |
| rs34973760 | snp | C/T | 0.188 | 0.24219 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869115 | TGAACTTTAGGCAGC[C/T]ATGAGGCCAATCCTG | 23092 |
| rs34979649 | in-del | -/G | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768901 | TAGAGATGGGGGGGG[-/G]TCTCGCTGTGTTGCC | 23092 |
| rs34986992 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858836 | AGGAGACTGCTTCCC[-/C]TGAGGAAGTGACCCT | 23092 |
| rs34988983 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838101 | CCGTCTACTAAAAAT[-/A]CGAAAATTAGCTGGG | 23092 |
| rs34997791 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065801 | GGCATTCACACACGG[-/G]ATACGCTGGGACAAG | 23092 |
| rs34998175 | snp | A/G | 0.235564 | 0.249583 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932829 | GTCAGGCTGGATAAT[A/G]CCAGCTGATTTGTGT | 23092 |
| rs35004108 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162721 | AACTGTTGAATATTT[-/T]GCTACTGTAGCCTAA | 23092 |
| rs35009928 | in-del | -/A | 0.375 | 0.216506 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818232 | TAAAAAAAAAAAAAA[-/A]GTCACTCTGGTTTAA | 23092 |
| rs35015063 | snp | C/T | 0.00685413 | 0.0581385 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143121021 | ACCAAGGTTTGCCAC[C/T]GTCATCAAATTCTGC | 23092 |
| rs35021956 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187415 | TTTATGAGATCATGG[-/C]AATGGCATTTCACCT | 23092 |
| rs35025097 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836257 | GCTTTTCACTTAATC[-/C]TGTGGTTCATTCTTC | 23092 |
| rs35034042 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112154 | GTATATTTATAATTC[-/C]AGTAAGTACCAGAAA | 23092 |
| rs35041379 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188236 | GCATTCACACTTCCC[-/C]AGTCATTTCCAGAGC | 23092 |
| rs35041428 | snp | C/T | 0.237014 | 0.249662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991534 | ATCACCTGTCTTCTG[C/T]GTCACTCACACTGGG | 23092 |
| rs35059079 | in-del | -/AAAT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176141 | AATAAATAAATAAAT[-/AAAT]GAAATATGACACGTG | 23092 |
| rs35066109 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814824 | TTACCACACTGGTTG[G/T]TGTGACAATCAGATG | 23092 |
| rs35072420 | in-del | -/A | | | intron-variant, frameshift-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143172981 | CGAGTTCAGCAAGCA[-/A]GTTACCATGTCTACG | 23092 |
| rs35079428 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219509 | ATGAATACTATGTGG[-/G]AATGTACTATGAGCA | 23092 |
| rs35079527 | in-del | -/C | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970403 | ATTCCAGAAGTAGCC[-/C]TTTGACTCTTTCTGT | 23092 |
| rs35091741 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121497 | TGAACCTCATTTTGG[-/T]AAACATGCTTTGCCC | 23092 |
| rs35099513 | in-del | -/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224119 | TTACTTTTTTTTTTT[-/T]GAAAAGATAAACTTG | 23092 |
| rs35100845 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834623 | ACAGGGCCCCTCCCC[-/C]ATGTAGTCTTTCATC | 23092 |
| rs35120620 | snp | C/T | 0.105924 | 0.204309 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840855 | CTTTTTCTTGCCTTC[C/T]TCCTCCAAAGAAAGG | 23092 |
| rs35130858 | snp | A/C | 0.125528 | 0.21681 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931887 | GGGCCATCCTTTCTG[A/C]GAGTAGAAGGTGGCT | 23092 |
| rs35136598 | snp | A/G | 0.164873 | 0.23506 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866549 | AAGGTGAGTTTGGGT[A/G]GCCCAAATTATTTTT | 23092 |
| rs35136715 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815972 | TTGTTTTTTTTTTTT[-/T]AATTTTTGTAGAGAT | 23092 |
| rs35139280 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124785 | GGTGGGAGGAGCAGT[-/T]GTGTGCACACAGGCG | 23092 |
| rs35142931 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167308 | AAAAAAAAAAAAAAA[-/A]TTAGCTGGGCCTGAT | 23092 |
| rs35165195 | in-del | -/T | 0.431621 | 0.171796 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931636 | GGATATTTTCTCCTC[-/T]TTTTTTTATCTTGAG | 23092 |
| rs35178883 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928232 | TTTGTGTGTGTGTGT[-/G]TTTTTTTTTTTTTTT | 23092 |
| rs35190505 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059958 | AGGATATGAATGAGC[-/C]AGTGTTGAATCCAGT | 23092 |
| rs35195724 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948425 | ATATATATATATATA[-/A]TATGTATTTTAATTT | 23092 |
| rs35196407 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997695 | TGCTGGGATTAGAGG[-/G]TGGGAGATACTGCAC | 23092 |
| rs35201189 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087659 | TTTTTTTTTTTTTTT[-/T]TTTGAGACGGAGTTT | 23092 |
| rs35202203 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948001 | GGCCACTGCACTCCA[-/A]GCCTGGGCAACATAA | 23092 |
| rs35205167 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083840 | ATATATCTTTCTCCC[-/C]ATCTTATATCTCAGA | 23092 |
| rs35219898 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224399 | GTTTTTAAGCATCCC[-/C]TTGGGCTTTGGATTT | 23092 |
| rs35225426 | snp | A/G | 0.0995161 | 0.199636 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191982 | CCTTCCCTGTCTGCC[A/G]GCAGTCTTACCCTTG | 23092 |
| rs35230004 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025895 | TTTTGTTTCTGTTCC[-/C]TGCTACCTATTTTAC | 23092 |
| rs35233031 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170933 | ATCAGATGCTGGGGG[-/G]AGTTTGGGGAGACAA | 23092 |
| rs35236196 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835052 | CTAGTAGGGGATGTA[-/A]TTGTCTCCATCTGAT | 23092 |
| rs35237495 | snp | A/G | 0.215747 | 0.247642 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967548 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 23092 |
| rs35240572 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074197 | ATTAGTGACCTTTCC[-/C]TGTTATATAGAACTG | 23092 |
| rs35244313 | in-del | -/AGGA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221947 | GGAAGGAAGGAAGGA[-/AGGA]TGGAAGGATGGATAC | 23092 |
| rs35250313 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083625 | GCCTCAGCCTTCCAA[-/A]GTAGCTGTGATTACA | 23092 |
| rs35251228 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164283 | AAGAGAGACTGTGCC[-/C]TTGCCATGGGTCAGG | 23092 |
| rs35253881 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178905 | AAGGAGTCTCACTCT[-/T]ATCACCCAGGGTGGA | 23092 |
| rs35256152 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144149 | AGCCTATAATTTTTT[-/T]CCTTCAGCAACATAA | 23092 |
| rs35258938 | in-del | -/CCTCTCT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949336 | AATATGTTCCTCTCT[-/CCTCTCT]ATGAACAGGCTCAGG | 23092 |
| rs35266419 | in-del | -/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007194 | CAAGACTCTGTCTCC[-/G]AAAAAAAAAAAAAAA | 23092 |
| rs35267021 | in-del | -/ATTTT | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980401 | ATTTTATTTTATTTT[-/ATTTT]TGAGATGGAATCTTG | 23092 |
| rs35268594 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020834 | TTAGTAGAGACGGGG[-/G]TTTCACCGTGTTAGC | 23092 |
| rs35285852 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827893 | ATTCTCCTGGCATCC[-/G]GGGAAGTGTAGATAC | 23092 |
| rs35292825 | in-del | -/T | 0.430732 | 0.172731 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928262 | TTAAAACTCATTGCC[-/T]TTTCCATCTCTTGAG | 23092 |
| rs35293378 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935051 | TCTTCCTACAATAAG[-/T]CATTATGGATTTTAT | 23092 |
| rs35309894 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045644 | ATGTGCCAGGTACTG[G/T]GTAAGATTTGGTTTA | 23092 |
| rs35312246 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108075 | TAAGAGGAACTGTTG[-/G]TATCCCTTAGGCTTG | 23092 |
| rs35315311 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784924 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 23092 |
| rs35319504 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023213 | TCAGAGCAAACTCCC[-/C]TGATGGCGTTTTATT | 23092 |
| rs35325569 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181151 | GGCTCATTCTCTACT[-/A]CTGAAACCTGTGGGA | 23092 |
| rs35331648 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785162 | TGTCGATCTCCTGAT[-/G]CTCGTGATCCGCCCA | 23092 |
| rs35343514 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797835 | CTTTTCAAACTTTAA[-/A]TGTGCATCCAGATTG | 23092 |
| rs35345843 | in-del | -/CA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122449 | TAAAATTATAATCCC[-/CA]AACTTCCTGCATTCC | 23092 |
| rs35357118 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975421 | TGGGGTTTCACATTC[-/C]AATTTTTATCTGTCT | 23092 |
| rs35368170 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002040 | CTGCCTCTCCAAGGG[-/G]CATTGTGGGGATGAA | 23092 |
| rs35369919 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108643 | GTGAAAGTACATTCC[-/C]ATTTCAAAAATATGC | 23092 |
| rs35370819 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092564 | CCCACCTTTTTTTTT[-/T]CTCAAAAATGATAAC | 23092 |
| rs35370982 | in-del | -/AT | 0.49987 | 0.00805196 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948410 | ACTTGTGTGTATTAA[-/AT]ATATATATATATAAT | 23092 |
| rs35376912 | in-del | -/A | 0.4776 | 0.103433 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927331 | CCCATATCTCTTTTC[-/A]AAAAAAAAAAAAAAA | 23092 |
| rs35382497 | in-del | -/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178889 | ATTTTTTTTTTTTTC[-/C]AAGGAGTCTCACTCT | 23092 |
| rs35405373 | in-del | -/C | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865074 | TGAGGGAGTTTTTCC[-/C]TGTGGTGACCTTCTG | 23092 |
| rs35421636 | snp | A/G | 0.127599 | 0.217986 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141108 | TTCCTGTTGTCACAC[A/G]GGCTGCAGAAGGTGT | 23092 |
| rs35426739 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026295 | TCTCATGGAGCATAT[A/C]CAATGAAAAGAAATT | 23092 |
| rs35435469 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000839 | AGTGAGAACACATGG[-/G]ACACAGGGAGGGGAA | 23092 |
| rs35441728 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976082 | AAATTCTCACTCTAT[-/A]CTGGATTTTGCCTTA | 23092 |
| rs35442053 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850337 | TCCTTTCAGTGGGGG[-/G]CAGTTTCTCCTCTGA | 23092 |
| rs35472528 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806676 | CGACATCACAGTGAA[-/A]GATTAGTGCAACGAA | 23092 |
| rs35486323 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908687 | GGGGGAGGAGGTAGA[-/G]CCCTGCCTCTCCATG | 23092 |
| rs35487324 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930039 | TCCCAGGCACAGCCC[-/C]AGTTCAGATTGAGTA | 23092 |
| rs35488201 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083557 | GGCTGAAGTGCAGGG[-/G]ACACAATCTTGGCTC | 23092 |
| rs35498070 | snp | A/G | 0.125182 | 0.216612 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849094 | TTATCAAATGTGTTT[A/G]TTACCCTCTTCTCTG | 23092 |
| rs35502317 | in-del | -/T | 0.392511 | 0.205404 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855882 | CTCTCCAGTGACTTA[-/T]TACCAGGAATGTAGG | 23092 |
| rs35506670 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075332 | TATAAATATAATTTT[-/T]ATTAAAAATATGTAT | 23092 |
| rs35508295 | in-del | -/C | 0.179425 | 0.239831 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153791 | TTCCGTCTTAACACA[-/C]ACGCTCATGCATTTC | 23092 |
| rs35510766 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091579 | TCCTGTATGACTTTT[-/T]ATACCAGATAAACTA | 23092 |
| rs35518380 | snp | C/T | 0.109461 | 0.206758 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836076 | GGAATGGAATCTTCA[C/T]GTACATTGACTTGGT | 23092 |
| rs35518665 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917665 | TGTTCCATGAATGGT[A/T]TTTTGGTTTCTGTAC | 23092 |
| rs35520934 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198529 | GCCCATTTAACCTTT[-/G]CTGACCCTTTCCCTT | 23092 |
| rs35522066 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793225 | AGAAGCAGGAGAATT[-/G]TGCCCACTGATTGTT | 23092 |
| rs35524868 | snp | C/T | 0.491368 | 0.0651254 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213187 | TGTATAATATCTGCA[C/T]ATCTGGGTAGAACCT | 23092 |
| rs35532623 | snp | A/G | 0.130351 | 0.219509 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912746 | GCAGTTTCAGCTATG[A/G]TCAGTGCTGTGATGG | 23092 |
| rs35543343 | snp | A/G | 4.99621e-05 | 0.00499786 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143147368 | ACAGTGAGTTGGGCC[A/G]GGTGGGTTTGACCAC | 23092 |
| rs35546646 | snp | A/G | 0.121717 | 0.214577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814994 | CATCATATTACTTAC[A/G]GAATTACATGATTTT | 23092 |
| rs35548612 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872403 | TTTCCCTCCCTTGGG[-/G]CATTTGGACATAATG | 23092 |
| rs35548690 | snp | A/C | 0.497829 | 0.0328757 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076921 | TTTCTAAAGTTTTTA[A/C]CATTATAAGCAATGC | 23092 |
| rs35568901 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784239 | GGTTCCCCAGCAGGG[-/G]AAGCTCTGCTCCATT | 23092 |
| rs35596823 | snp | A/C/G | 0.112058 | 0.210126 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182739 | TCCCTTGCTCTATGT[A/C/G]TGTGGTGGCCTGGCC | 23092 |
| rs35601213 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022379 | GCCTGGCCAATCCCC[-/C]TGATTTTACAAATGT | 23092 |
| rs35603609 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083145 | CTTCCTTTTTCTTTT[-/T]CCCATTAGTCACAGG | 23092 |
| rs35617606 | in-del | -/T | 0.439918 | 0.162576 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786148 | GCTAATTAAAAAACA[-/T]TTTTTTTTTTTTTTG | 23092 |
| rs35632331 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189770 | GATATTTTTCTCCTC[C/T]ACCAGCCTGTGTTCT | 23092 |
| rs35639847 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833411 | CATGTTCATGTACTT[-/G]TTAAATGTGTACTGT | 23092 |
| rs35642579 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813135 | TTTAGTAGAGATGGG[A/G]TTTCACCGTGTTAAC | 23092 |
| rs35645150 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878544 | GTGTGTGTGCACGCA[-/TG]TGTGTGTGTGTGTAT | 23092 |
| rs35677404 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013176 | CTCTCTTAAAAAAAA[-/A]CTTATTCTTCTGATT | 23092 |
| rs35679838 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199042 | TAAAATGCATTTCCC[-/C]TATTATTGTTAAGAC | 23092 |
| rs35680556 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095994 | TGGATATTCTTTTTT[-/T]AAAACTCTACCAACA | 23092 |
| rs35702862 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220058 | CCCAGTACCTGTGCT[-/T]GTGGGTGAACAGCTA | 23092 |
| rs35711054 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091482 | TCCTTGGTACCTTTT[-/T]ACTGAGAAATTTCCT | 23092 |
| rs35718935 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109475 | TGTATTTTTTTTTTT[-/T]AGACAGCGTCTTGCT | 23092 |
| rs35722079 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105988 | TTGAATCCTGACTTT[-/T]CGCAGAGTAGCAGGA | 23092 |
| rs35724160 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111934 | TGACGTGTTTAACCC[-/C]AGGTACCTAGTGCAG | 23092 |
| rs35744364 | snp | A/G | 0.395635 | 0.2032 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868875 | TGGAGACTCTCAGGT[A/G]TTCCACCTGTAAGCC | 23092 |
| rs35745002 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876320 | TGCATTTTCTATTTT[-/T]AACCCCCATGATGAC | 23092 |
| rs35750293 | multinucleotide-polymorphism | GA/TT | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026992 | GTGGTGTGTGAATTG[GA/TT]TATAGGGTGTGAGAG | 23092 |
| rs35752172 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020599 | TAGTCCTTTCTTTCC[-/C]TTGTGGTTTGTTTTT | 23092 |
| rs35754059 | in-del | -/CA | 0.375 | 0.216506 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898191 | ACACACACACACACA[-/CA]TATATACACACACAT | 23092 |
| rs35754063 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044616 | GACGGGGTTAGTCCC[-/C]TGAAACCCAGTGGAC | 23092 |
| rs35757589 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144169 | AGCAACATAATTGCC[-/C]ATCAGTCCTTCTTAT | 23092 |
| rs35764289 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945001 | CCAAATGTGCACTCC[-/C]TTACCTCTCACCTGG | 23092 |
| rs35765170 | in-del | -/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869543 | AAAACATTTCAAGGG[-/G]TAGTTAATACACAAT | 23092 |
| rs35771003 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786523 | GGCTGGTCTCAAATT[-/A]CCTGGCCTCAAATGA | 23092 |
| rs35776414 | snp | A/G | 0.170704 | 0.237936 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858827 | AGGGAATGCGAGGAG[A/G]CTGCTTCCCTGAGGA | 23092 |
| rs35783443 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142919198 | CGATATTACCATTGT[-/G]CCTTGTAAAAAGGGG | 23092 |
| rs35800463 | snp | A/G | 0.046775 | 0.145601 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167416 | GAACCCGGGGGGGAA[A/G]AGGTTACAGTGAGCT | 23092 |
| rs35803857 | in-del | -/AA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097822 | CGAGACTCCAACTCA[-/AA]AAAAAAAAAAAAAAA | 23092 |
| rs35805895 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131152 | GAGTGAACTTCTCCC[-/C]TTGTTTGTTACCATG | 23092 |
| rs35809279 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896468 | AAACCTCATACAACA[A/G]TAGATGTTTACTTCT | 23092 |
| rs35809624 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858791 | CTGGGGAGCTATGAG[-/T]AGTGTACCCCTGGGG | 23092 |
| rs35809781 | in-del | -/C | | | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859436 | TTCTGGTTTCTTTCC[-/C]TGATGTGTGGTGGTA | 23092 |
| rs35832241 | in-del | -/GA | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226787 | CGAGTGCTTTTCGGT[-/GA]GAGGCAAAGAGAAAG | 23092 |
| rs35870752 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869101 | ACTTTGGTATTCTTG[-/C]AACTTTAGGCAGCCA | 23092 |
| rs35901802 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871018 | AGGTGAGTTCCTTTT[-/T]CAGGTCCATTCATCA | 23092 |
| rs35902121 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124130 | CAAGCCCTACTACAG[A/G]GCTAAAGTATATACC | 23092 |
| rs35905534 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185247 | TGTATGGATACATAT[-/A]TACACAAAGAAAGGT | 23092 |
| rs35906058 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127518 | ATCGGTGCCCCTTTT[-/T]AATGTGTTAACTTTC | 23092 |
| rs35908298 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207527 | CAAAGCTGGCCAGGG[-/G]ACAACAGGGGGCTGC | 23092 |
| rs35912852 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113602 | GCCAGCTATAAATGG[-/G]AATGCCATCATATTT | 23092 |
| rs35921990 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917057 | TTTTTTTTTTTTTTT[-/TT]AGATGGAGTCTTGCT | 23092 |
| rs35932484 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975848 | TGAGGTGTACCATAC[A/C]TGTATTTATCTTACA | 23092 |
| rs35940573 | snp | A/C | 0.486725 | 0.0803809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213273 | ATTGTAAACATTCAA[A/C]GGACATGAGAAAAGC | 23092 |
| rs35945833 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009978 | TCTCAAGAGGCTTAC[C/T]TGAAAGCATATAAAT | 23092 |
| rs35950662 | in-del | -/TTT | 0.5 | 0 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865499 | TTTTTTTTTTTTTTT[-/TTT]GAATCCCTTATAACT | 23092 |
| rs35958777 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123473 | TTTGTATAAACTCCC[-/C]TGCCAATAGAACTTA | 23092 |
| rs35965009 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090257 | ATGCAGCCCATGCCC[-/C]GGTTGACTGGAGGAC | 23092 |
| rs35967916 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170655 | ATTTAATCAACATAA[-/A]TGCCGGAGGTACTGT | 23092 |
| rs35995107 | snp | A/G | 0.0626037 | 0.165477 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216388 | CTTCAGTGGCCTCCC[A/G]TTGCTCTGAGAATTA | 23092 |
| rs36015018 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126663 | CTTCCTAAGGGGAAA[C/T]ACTAGCTCATAGCAT | 23092 |
| rs36019923 | in-del | -/A | 0.402277 | 0.198272 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778960 | AAAAAAAAAAAACTT[-/A]GTGTGTGTGTATGTG | 23092 |
| rs36019985 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011989 | AGTTAGTCAGAAAAA[-/A]CCTATCATCGCCCAC | 23092 |
| rs36025229 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798273 | CAACAGGACCCTTTT[-/T]CTGCTCCCTTTGATG | 23092 |
| rs36039558 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815411 | CACTTTAGTCTTTTT[-/T]AGAGAACAGCAGTTA | 23092 |
| rs36045118 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119304 | TTGTTGATTCACTTG[-/G]CACACGGGACTTTTG | 23092 |
| rs36049761 | in-del | -/A | 0.473451 | 0.112115 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880518 | CAAGACTCCATGTCC[-/A]AAAAAAAAAAAATCA | 23092 |
| rs36055427 | snp | A/G | 0.225597 | 0.248806 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128800 | TCAGTCTCATTTCTC[A/G]TATAAACCTTTCTGT | 23092 |
| rs36081768 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077868 | AGCTGTTGGTGCCTA[A/G]GCTCTTCTTTTCTGG | 23092 |
| rs36091019 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107198 | TTTAGGAACAGACAG[-/C]AAGGCCAGGGTAGTT | 23092 |
| rs36097516 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141824 | ATTCATCAGAGGCCC[-/C]ATTCCTCCTTTGCGG | 23092 |
| rs36220244 | in-del | -/AGGGT | 0.482979 | 0.0906686 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907595 | TTCTAACATAGTTTA[-/AGGGT]AGGGTAGATGAGCAT | 23092 |
| rs41290619 | snp | A/G | 0.0503692 | 0.150491 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121188 | TGAAGAATGTACCTG[A/G]GGGGAAGCTGCATTG | 23092 |
| rs41517244 | snp | A/C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166796 | TTGGCAGTCTTCGAA[A/C/T]GTGCTCTACCTTCAG | 23092 |
| rs55634781 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859949 | ATGGTAGGTGTAACC[C/T]CTCAGGGCTGTCAGC | 23092 |
| rs55651637 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819259 | TAATTACAAATTCCC[A/C/T]TGAAGAAAAGCAGAT | 23092 |
| rs55662035 | snp | A/G | 0.262435 | 0.249691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124832 | CGTTATCTCTGCAGG[A/G]GATCTATGGTACCCA | 23092 |
| rs55674118 | snp | A/T | 0.0535932 | 0.154675 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115218 | TGCACCTGTAATCCC[A/T]GCTACTCCGGAGGCT | 23092 |
| rs55675814 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884882 | CTTAGTCTAGACTTG[G/T]CTCATTCAAGCTGTG | 23092 |
| rs55680810 | snp | C/T | 0.125528 | 0.21681 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024578 | TTCCCCCACTGCCAC[C/T]GAGTACAGGCTTCCA | 23092 |
| rs55691649 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814296 | CTGTTCTTCCTGTTA[C/G]ATGTGCTGTAAACAG | 23092 |
| rs55703682 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813157 | CGTGTTAACCAGGAT[A/G]GTCTTGATCTCCTGA | 23092 |
| rs55740726 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197494 | GCACAGAAAGGTTGA[A/G]TGCCTTTTCTTTTGG | 23092 |
| rs55760974 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962046 | CTGCTGTGTTTGGTA[C/T]TGAGACTGAGTTAAT | 23092 |
| rs55774021 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843973 | TGATAACTGTCTCCT[C/T]CCATTGTTGTGGGGA | 23092 |
| rs55774141 | snp | A/G | 0.375996 | 0.215928 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209660 | GTGGTGGGCGCCTGT[A/G]ATCCCAGCTACTCAG | 23092 |
| rs55795909 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783071 | GACCACACATTAGGT[C/T]TAAATAGGTCAGCAG | 23092 |
| rs55844249 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846689 | AGAGACTTACATTTT[A/G]TGCTGTCCTGTGAGA | 23092 |
| rs55877614 | in-del | -/A | 0.455024 | 0.143057 | intron-variant, downstream-variant-500B | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142972181 | AGCGAGATTCCATCT[-/A]AAAAAAAAAAAAAAG | 23092 |
| rs55936057 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933616 | CAGTCATTGCCATTT[-/T]CCAGCCAGAAAATGA | 23092 |
| rs55937424 | snp | A/G | 0.100588 | 0.200439 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061989 | GATTATTTTCCACCC[A/G]ACAAGATTTATCTGA | 23092 |
| rs55943714 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963274 | TTGATGGGCATTTAG[A/G]TTGATTCCGTGACTT | 23092 |
| rs55961768 | snp | G/T | 0.473909 | 0.111197 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813496 | TGTGTGTATTAATCT[G/T]CTAGGGCTACCATAA | 23092 |
| rs55977204 | snp | C/T | 0.295088 | 0.245901 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121530 | TTCTTACTTGATTGT[C/T]TTCTTATGAATTTAT | 23092 |
| rs56009134 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939794 | ATTGTGATAATAATA[A/G]CCCCTACCTCATAAG | 23092 |
| rs56048610 | snp | A/G | 0.231775 | 0.249335 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983799 | TCATTATGTGTTTAT[A/G]TATATCTAGACACAC | 23092 |
| rs56059604 | snp | A/G/T | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142770205 | TGCGCTGCGGACCTA[A/G/T]GCGTTGGCGAGGGCC | 23092 |
| rs56092934 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870246 | GTGTGTTAGATTCCT[A/G]TGTGCATCAGAGGGA | 23092 |
| rs56099057 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865214 | TTCATCGGAGATCCA[A/G]TGCTGACTAACTCAC | 23092 |
| rs56114785 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221444 | AAAAAAAAAAAAAAA[-/A]CCCCAGAAAATTTGC | 23092 |
| rs56116431 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097383 | AAAAAAAAAAAAAAA[-/A]GAGCATATCTGACTG | 23092 |
| rs56117738 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196177 | ATTTAGTAACCACCC[C/T]CTCACCCCCCACTGG | 23092 |
| rs56121326 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850283 | CCTTGGTCAATTCCT[C/T]TGTGACCAGTTTAAC | 23092 |
| rs56160167 | snp | G/T | 0.180064 | 0.240019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031157 | CAGCCAGTGTGGCTA[G/T]GTGCTCAGAGCTGGC | 23092 |
| rs56182620 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974162 | GACTTTGGTCATTCC[A/G]TTGCTATCCTGTTCC | 23092 |
| rs56211069 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893003 | GCTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 23092 |
| rs56237402 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043401 | TTTTATTGCTGAGTA[-/A]TATTCCATTGTATGG | 23092 |
| rs56238527 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156874 | CTTTCCATCTCCCCC[C/G]AAAAGCCCAGTCAGC | 23092 |
| rs56244122 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177683 | CAGAGCCACTTGAAA[-/A]CAGTTTGCAGAGTGT | 23092 |
| rs56274884 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021518 | GATCATTCTCTTTGG[G/T]TAGATTCCGCCACGT | 23092 |
| rs56276411 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202729 | GTACCAAAACAGATA[C/T]ATAGATCAATGGAAC | 23092 |
| rs56288427 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204475 | GTTGCAGTGAGCCAA[A/G]ATTGTGCCATTGCAC | 23092 |
| rs56305476 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108686 | TTATTTCCCTCATTT[A/T]AAAAATCCCCACAAA | 23092 |
| rs56345019 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116001 | GATAAAAATAGAATC[-/A]GACAGGATAAGATGG | 23092 |
| rs56376127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122487 | TTTTATTCCACTTAG[C/T]CTGTTTTCATATCAA | 23092 |
| rs56383536 | snp | C/G | 0.125874 | 0.217008 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025336 | CCTGCCCTTCGCTGC[C/G]TCAGAGTTTGTTGTG | 23092 |
| rs56394028 | snp | C/T | 0.265727 | 0.249505 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089767 | GCAGCTATTTTATTT[C/T]GGGCTTGAAATTGTT | 23092 |
| rs56394878 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999926 | ATAAAACTCAGTAAT[A/C]AAAAGAAGAACCTAA | 23092 |
| rs56404805 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012364 | AGTGACACAAAGCAG[A/C]TGAAGGGCCAAGTGG | 23092 |
| rs56660252 | snp | A/G | 0.115438 | 0.210697 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862007 | GCTCCAGGTTCTGCC[A/G]TCTGTGACTTTCCGA | 23092 |
| rs56712199 | in-del | -/AGGAAGGA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221950 | GGAAGGAAGGAAGGA[-/AGGAAGGA]TGGAAGGATGGATAC | 23092 |
| rs56737096 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996396 | TACTTAGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 23092 |
| rs56740224 | in-del | -/TTTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157188 | TTTTTTTTTTTTTTT[-/TTTT]CTCGAGACAGAGTCT | 23092 |
| rs56806338 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062122 | ACAGAGAGTATTAAG[A/T]CTATTGCATGGTGTG | 23092 |
| rs56809185 | snp | A/G | 0.222035 | 0.248431 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093771 | AGGGGAGGGACCAGC[A/G]GGAGTGGAGCTACTC | 23092 |
| rs56852430 | in-del | -/AAAAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085062 | AAAAAAAAAAAAAAA[-/AAAAAA]GAAACGCTTTCTGCA | 23092 |
| rs56868024 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133931 | TCTTCCCAGTCCACA[A/G]ATGTGAGTAACCTTG | 23092 |
| rs56868806 | snp | A/C | 0.0299026 | 0.118636 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196109 | TGAAATATAAATGTA[A/C]GTCTTAACAAATTAT | 23092 |
| rs56883765 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005732 | AAAGTTTATTTTTCT[A/C]TTCATCATCATTGTT | 23092 |
| rs56893894 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202275 | TGCTTTTTTTTTTTT[-/T]CCATTTGCTTGGTAA | 23092 |
| rs56895767 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839242 | TTATGCTGTAATTAA[C/G]ATTTGATTTTCACAG | 23092 |
| rs56928930 | snp | G/T | 0.106633 | 0.204807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026991 | GTGGTGTGTGAATTG[G/T]ATATAGGGTGTGAGA | 23092 |
| rs56930910 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224695 | TTAAAGAACCAGCTT[C/G]TTAGAATGTTCAGTT | 23092 |
| rs56941301 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793274 | TTTTTTTTTTTTTTT[-/T]AATCTATCTTTCTTT | 23092 |
| rs56962078 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928219 | TATGATTAGGACTTT[G/T]TGTGTGTGTGTGTTT | 23092 |
| rs56967719 | snp | C/T | 0.234401 | 0.249513 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089923 | GAAAGGGATAGCCAA[C/T]TGGACTAAAGCATAA | 23092 |
| rs56968663 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808463 | TTTTTCTCATCAGTT[A/T]AACATTTGCCATAGT | 23092 |
| rs56994836 | in-del | -/TATACATACATA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012543 | GGATATATTTATATA[-/TATACATACATA]CATACATACATATAT | 23092 |
| rs57064036 | snp | A/G | 0.213937 | 0.247385 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065806 | TTCACACACGGATAC[A/G]CTGGGACAAGGGGAA | 23092 |
| rs57064748 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050823 | TCTGGGAGCTAGCAA[C/T]ACGGCTACTAATCAC | 23092 |
| rs57078655 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054746 | CTGAGTGATTTAGGA[A/G]ACTTTGTTCTATATG | 23092 |
| rs57170643 | snp | A/G | 0.241053 | 0.24984 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938164 | ATAGTTTTAAAAGAT[A/G]GTATCATTGGATTAT | 23092 |
| rs57175122 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062538 | ATGTTGTAGCTTGGG[-/T]TTTTTTTTTTTTTTT | 23092 |
| rs57236342 | snp | C/T | 0.117537 | 0.212022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062007 | AAGATTTATCTGAGC[C/T]ACTTGTGGGAGGATT | 23092 |
| rs57253759 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951000 | TCCTCTTTCCCTTTC[C/T]CTTTCCCTTTCCCTT | 23092 |
| rs57310752 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124016 | GGTGACTCTTCTTCT[A/G]TCTAGTCTTAGTGTC | 23092 |
| rs57325229 | snp | A/G | 0.118584 | 0.212673 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189368 | CTTTGTTGAGATCTC[A/G]GCTCAGATGTCACCC | 23092 |
| rs57388408 | in-del | -/TAG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907460 | AAGACCCACTGGATG[-/TAG]CATCAATGGGAAACA | 23092 |
| rs57389427 | snp | A/C | 0.105924 | 0.204309 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841605 | CCCCAGGTCTGATGG[A/C]AACTGTAGATTTCTT | 23092 |
| rs57426420 | snp | C/G | 0.499897 | 0.00718776 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040589 | TAATCAAATAACAAA[C/G]ATAATTTCAGATATT | 23092 |
| rs57433366 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082884 | CCTTTTCTACAGAAC[A/G]TCACGGGTTTTTGAG | 23092 |
| rs57453637 | snp | G/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867332 | GTGTGTGTGTGTTTT[G/T]TTTGTTTTTGCTAGT | 23092 |
| rs57462040 | in-del | -/T | | | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193265 | TTTTTTTTTTTTTTT[-/T]GAGGCAGAGTCTCGC | 23092 |
| rs57464790 | snp | A/G | 0.116138 | 0.211142 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066375 | AAGCGATGCGTGACT[A/G]TACTTCAAGTCTCTT | 23092 |
| rs57549608 | in-del | -/CT/TC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898619 | TCTCTCTCTCTCTCT[-/CT/TC]TTTGCCAAGAAGCTC | 23092 |
| rs57552092 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097221 | GTGCGTGCCTGTAAT[C/T]TGGGGTGGGGCAGGG | 23092 |
| rs57605274 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985448 | ATTGACTCTCCCAGA[A/G]CAACTTCCAGTCCTG | 23092 |
| rs57615257 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132561 | GAATGAGGAAATACT[A/G]TATAATGTTAGATGA | 23092 |
| rs57638651 | in-del | -/T/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923098 | GGAGTTTTTTTTTTT[-/T/TT]CTTTTAATTAAATGA | 23092 |
| rs57666289 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769962 | TTTGAGTGTAAAATC[A/G/T]GTTGCCCCGCAGTGC | 23092 |
| rs57706003 | snp | A/G | 0.33533 | 0.234987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124747 | AGCCAGATTCAAGGC[A/G]GGGGGAGCTAGATGC | 23092 |
| rs57707307 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032304 | GGGAAGTAAACCAGC[C/T]GAAGCCTCAACTGCA | 23092 |
| rs57707373 | snp | A/G | 0.312104 | 0.242163 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040590 | AATCAAATAACAAAC[A/G]TAATTTCAGATATTG | 23092 |
| rs57733343 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142898 | TCCTGACCACAGCAC[A/G]GGAAAGCCTCTGGGT | 23092 |
| rs57777709 | snp | A/T | 0.327914 | 0.237549 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085012 | ATCGCGCCACTGCAC[A/T]CCAGCCTGGGCAACA | 23092 |
| rs57787106 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951010 | CTTTCTCTTTCCCTT[C/T]CCCTTTCCCTTTCTC | 23092 |
| rs57835905 | snp | C/T | 0.122411 | 0.214991 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806450 | AACGGTTGTACATGG[C/T]ATAATAAGTTATAGG | 23092 |
| rs57882388 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190035 | CAGAAGGAGGGGGGG[A/G]AAAAAAAAAAAAAGA | 23092 |
| rs57919462 | snp | A/G | 0.379158 | 0.214052 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205870 | GACACTGGATATTTT[A/G]GACACTGGATATACA | 23092 |
| rs57937559 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912075 | TTAGATAAAAAAGAT[-/T]GACAGAGGCAGGAGA | 23092 |
| rs57949069 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012556 | ATACATACATACATA[C/T]ATATATATATATATA | 23092 |
| rs57985646 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784989 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 23092 |
| rs58029071 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876863 | GCCCTACGGAAAGAC[C/G]ACTTTCTCTTGATTG | 23092 |
| rs58036254 | snp | A/T | 0.093417 | 0.194889 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789049 | TAATGCCAACCCTTT[A/T]GCGTGGAACTATTGT | 23092 |
| rs58042104 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857170 | ATTGGATTTAGGACC[C/G]GTCCTAGTCCTATAT | 23092 |
| rs58052627 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929901 | CAGAAAGGAGGGTAA[C/T]TTTGCTCTCTAGGGC | 23092 |
| rs58066344 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800773 | GTGAACCTGGCAGCA[C/T]GTTCTCTTGTGCTCA | 23092 |
| rs58096008 | snp | A/T | 0.106633 | 0.204807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026992 | TGGTGTGTGAATTGG[A/T]TATAGGGTGTGAGAG | 23092 |
| rs58120046 | snp | C/T | 0.134802 | 0.221877 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048050 | GTCAAGGTTTCACCA[C/T]GTTGGCCAGGCTAGT | 23092 |
| rs58170825 | snp | A/G | 0.274124 | 0.248833 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100381 | TACATTGTGTGGGAA[A/G]TAGCGAAGGAACATC | 23092 |
| rs58179804 | snp | A/G | 0.170408 | 0.236992 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196984 | TGTATATATCCCTAA[A/G]TGCAACATTTTATTG | 23092 |
| rs58232229 | snp | A/G | 0.116138 | 0.211142 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177182 | TATATACAATCTAGA[A/G]TAAATGATAACACTT | 23092 |
| rs58252516 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799192 | GTGGGTTTTTTTTTT[-/T]GGAGGCATATTGTAA | 23092 |
| rs58269107 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158378 | GTTTACACAAAGAGC[A/G]TTGGTCAAAGCCCCC | 23092 |
| rs58337098 | snp | A/G | 0.149665 | 0.228982 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181828 | TTTAGCAATGCCTCC[A/G]ATTCAGGAATTTGTT | 23092 |
| rs58390522 | in-del | -/TGTGTGTG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858097 | GTGTGTGTGTGTGAG[-/TGTGTGTG]AGAGAGAGAGAGAGG | 23092 |
| rs58417688 | snp | C/G | 0.115088 | 0.210473 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066566 | AGAAAGAAGATGATA[C/G]AGCTGGTTTTAGGGT | 23092 |
| rs58436709 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092552 | AAATTCTCCCCCCCC[C/G]ACCTTTTTTTTTCTC | 23092 |
| rs58498824 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097383 | AAAAAAAAAAAAAAA[-/A]GAGCATATCTGACTG | 23092 |
| rs58502249 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854433 | TGTAGGTTTGGGGAA[C/T]GTAAGGACTATGTCA | 23092 |
| rs58550799 | in-del | -/AAAAAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808270 | AAAAAAAAAAAAAAA[-/AAAAAAA]TGTTGTATTTTAGGA | 23092 |
| rs58556479 | snp | C/G | 0.146985 | 0.227789 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831130 | TCTGTTTCTTTCTTG[C/G]TTTCTGTGGTTCCCT | 23092 |
| rs58576577 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963198 | TATATATATATATAT[-/AT]GTGTGTGTGTGTGTG | 23092 |
| rs58581074 | snp | A/G | 0.123452 | 0.215605 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157566 | ACATTTCCTAAATAC[A/G]TTGACCATAGTACAT | 23092 |
| rs58666775 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092264 | CGCCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT | 23092 |
| rs58681445 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987941 | ATATTCATCAGGGAT[A/G]TTGGCCTAAAATACT | 23092 |
| rs58693212 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079451 | AGGCAGGCAGGGAGA[A/T]CACCCAGGAAGCTCC | 23092 |
| rs58704906 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856914 | ATGAACTGGGTGGCA[C/T]AAAACAACAGAAATG | 23092 |
| rs58714071 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783234 | GGGTTTCAGAAGCGT[A/G]AAAGTTCTAGCAGCT | 23092 |
| rs58728915 | snp | C/T | 0.192715 | 0.243348 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831199 | GGATTCCACTGATCA[C/T]GATGGAGCCAGATCC | 23092 |
| rs58766330 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045024 | GAAAAGAAATATGAC[A/G]TTTTAGACTGGTTTG | 23092 |
| rs58800196 | snp | G/T | 0.0256215 | 0.110247 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867858 | TTGTCCTAACTTACC[G/T]GCTTTTTTTTTCACA | 23092 |
| rs58817012 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022294 | GCCAGGCTGGTCTCG[A/G]ACTCCTGACCTCAGG | 23092 |
| rs58831129 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800860 | CAGGGTGGGAGGAAA[A/G]CGGAGGCCGTGGCAG | 23092 |
| rs58841045 | in-del | -/TTT | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011324 | TTTTTTTTTTTTTTT[-/TTT]ACTTTCTCCAATGTA | 23092 |
| rs58889669 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035333 | AGAAACTTTGGTGTA[C/T]ATATATGATGGATTA | 23092 |
| rs58902362 | in-del | -/A/AA | 0.404209 | 0.196773 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016721 | AAAAAAAAAAAAAAA[-/A/AA]TTGGCCACTTTTTCA | 23092 |
| rs58956055 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077585 | TCATAAAAGGCTCAC[C/T]GTAGATGACTAGGAC | 23092 |
| rs58977665 | snp | G/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867325 | TGTGTGTGTGTGTGT[G/T]TGTTTTGTTTGTTTT | 23092 |
| rs58994031 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854940 | TTCAAAGGACCCCCC[-/C]AGTCCCTTTTGTTCT | 23092 |
| rs59037822 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776360 | TTTAGAACATTTTTA[A/G]CACCCCGAAAAGCTT | 23092 |
| rs59068659 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780665 | GAATGTAGGATCCCA[G/T]AGACCTTGTTTGTGT | 23092 |
| rs59134351 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943612 | CACATGAAATTTTTT[-/T]GGGGGAAGGCACACA | 23092 |
| rs59168054 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209781 | GCTAGACTCCATCTC[-/A]AAAAAAAAAAAAATA | 23092 |
| rs59186727 | snp | A/G | 0.0607341 | 0.163335 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143166595 | CTTTGGATTGCCATG[A/G]CCCCTGACAGCCCCA | 23092 |
| rs59203827 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216950 | CTCTACAGGAGAAAA[C/T]GAGGCATTACAGAAC | 23092 |
| rs59218126 | in-del | -/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867330 | TGTGTGTGTGTGTTT[-/G]TGTTTGTTTTTGCTA | 23092 |
| rs59232070 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769145 | TTATCGCTTGTTTGC[A/T]TCCATCTCACCTAAT | 23092 |
| rs59243502 | in-del | -/ACCTGAGGCTGA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032273 | ACTGAGCAGAGCTGA[-/ACCTGAGGCTGA]GGGAGGGAAGTAAAC | 23092 |
| rs59294958 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858875 | AATCTAATGGGCTAA[A/G]GGGCAGTAACTAGGT | 23092 |
| rs59303052 | in-del | -/TGTGTGTG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858095 | GTGTGTGTGTGTGTG[-/TGTGTGTG]AGAGAGAGAGAGAGA | 23092 |
| rs59330774 | snp | C/T | 0.318896 | 0.240319 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026709 | GTGAAGAGAAGTCAC[C/T]GGAGAGTTGTGATCA | 23092 |
| rs59464424 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092552 | AATTCTCCCCCCCCC[-/C]ACCTTTTTTTTTCTC | 23092 |
| rs59498324 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006317 | TTTAGTGTTTTTTCT[-/G]TTTTTTTTTTTTTTT | 23092 |
| rs59504374 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114132 | TAAGCATTCAATTAA[C/T]TATTTCAGGCTTCCT | 23092 |
| rs59608802 | in-del | -/CTTTTTTTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168458 | TCTTTTTTTTTTTTT[-/CTTTTTTTT]TTTTTTTTTTTTTTT | 23092 |
| rs59669579 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901179 | GAGGGGACATTAATA[A/G]TTTTTAAGTATATGA | 23092 |
| rs59672579 | snp | C/T | 0.287085 | 0.247234 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866576 | TTTTAAGGGGTATTT[C/T]ATCTAAATAGAATTA | 23092 |
| rs59710342 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876509 | GGCCAGGTGTGGTGG[C/T]TCATGCCTGTAATCC | 23092 |
| rs59744740 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140813 | TTAACTAGCTGCTGA[G/T]ATTATAGCTCTGAAT | 23092 |
| rs59748832 | in-del | -/T | 0.177802 | 0.239348 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029572 | ACCATGCCCAGCAAA[-/T]TTTTTTTTAACCTTT | 23092 |
| rs59774766 | snp | A/T | 0.109108 | 0.206518 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148055 | CCCACATTGCTTCAC[A/T]TGCTTCCTTAGACTA | 23092 |
| rs59808603 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801339 | AATAGAAATTGATGA[C/T]GCCCTATGTGCCAGA | 23092 |
| rs59835326 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900430 | AGAATCTAAGGGGAT[A/G]GATGGGCCGGGGACA | 23092 |
| rs59861739 | snp | A/T | 0.133435 | 0.221162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858092 | GTGTGTGTGTGTGTG[A/T]GTGAGAGAGAGAGAG | 23092 |
| rs59869860 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196226 | CTGGTGTCCACATCT[C/T]TTGCTTTCTCCTCCC | 23092 |
| rs59877334 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187671 | AGGCGGAGCACCAGC[A/G]CTTTCTGGCTCTTAG | 23092 |
| rs59889381 | snp | C/T | 0.408017 | 0.193729 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859423 | CTGTTTTCTTTCTTT[C/T]CTGGTTTCTTTCCTG | 23092 |
| rs59900779 | snp | C/T | 0.193653 | 0.243567 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190833 | AGAACATGGTGTCCA[C/T]AGAATGGAATAGAAT | 23092 |
| rs59922477 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788834 | GACAACTGCAGTAGA[A/G]TATCTCCACCATTTA | 23092 |
| rs59962768 | snp | C/G | 0.327914 | 0.237549 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085014 | CGCGCCACTGCACTC[C/G]AGCCTGGGCAACAGA | 23092 |
| rs59997098 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185463 | ATCCCTCCTTTTTTT[-/T]CTTTTACCAAAAACG | 23092 |
| rs60030682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863059 | AGATACTTTGGGAGG[A/G]ATCTTAGAGCTACGG | 23092 |
| rs60038561 | in-del | -/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923880 | TTTTTTTTTTTTTTT[-/G]ATACGGAGTCCTGCT | 23092 |
| rs60048104 | in-del | -/A | 0.329317 | 0.237084 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103571 | AATGTTAGACTGGAT[-/A]AAAAAAAAAATGTGG | 23092 |
| rs60064238 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084021 | TTTAAAGCATCTGCA[C/G]GCTCTCGCCGTCCAC | 23092 |
| rs60095874 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156512 | TCAGGCCTCACCCTA[G/T]ACCTATAGGATCAGC | 23092 |
| rs60101980 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210276 | AAGAGAGTTTGTGCA[C/G]GGAAACTCCCGTTTT | 23092 |
| rs60139914 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828202 | ACAATACTCAGGGGA[C/T]GAAGTATCTGTTAAA | 23092 |
| rs60166212 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950986 | CTTTCCCTTTCCCTT[C/T]CTCTTTCCCTTTCTC | 23092 |
| rs60171496 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784944 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 23092 |
| rs60196587 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869140 | ATCCTGTTGCAAGTT[C/T]TAACCTCAATGATGG | 23092 |
| rs60257351 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063092 | TGCCAGTGCAGGATT[A/G]CTTGGCCGCTGGGCC | 23092 |
| rs60259893 | snp | C/T | 0.138546 | 0.223781 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974801 | TCAACTATTTAGCAT[C/T]GTGAATAGTTTCCCC | 23092 |
| rs60269567 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027649 | TAAAAGTATAACTGA[A/G]AAATGTTTGTGAACC | 23092 |
| rs60278493 | snp | A/G | 0.179425 | 0.239831 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029771 | CCATTTCTCCCACAA[A/G]AAAGGTTTGGTTTGT | 23092 |
| rs60337511 | snp | C/T | 0.0490153 | 0.148678 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789044 | TGATCTAATGCCAAC[C/T]CTTTTGCGTGGAACT | 23092 |
| rs60428049 | in-del | -/TTTTT | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038710 | TTTTTTTTTTTTTTT[-/TTTTT]GAGACAGAGTCTCTT | 23092 |
| rs60428325 | in-del | -/ATT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202271 | CCCCTGCTTTTTTTT[-/ATT]TTTTCCATTTGCTTG | 23092 |
| rs60473595 | snp | A/T | 0.0962929 | 0.197165 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097176 | AAACCCCGTCTCTAC[A/T]AAAAATACAAAAATT | 23092 |
| rs60477396 | snp | A/C | 0.106278 | 0.204558 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106766 | GCATGAGCCACTGCA[A/C]CCAGCCTGGGCTTCA | 23092 |
| rs60569693 | in-del | -/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867323 | TGTGTGTGTGTGTGT[-/G]TGTGTTTTGTTTGTT | 23092 |
| rs60604891 | in-del | -/AA | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097837 | AAAAAAAAAAAAAAA[-/AA]GAAAATTACCCCACG | 23092 |
| rs60663530 | in-del | -/TTAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189590 | CCATTAGGATAATAA[-/TTAA]AATATTATCAAAAAG | 23092 |
| rs60683606 | snp | C/T | 0.231189 | 0.249291 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022157 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGCTCAG | 23092 |
| rs60790038 | snp | A/G | 0.146985 | 0.227789 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829307 | CCCTTTCTCGAAACC[A/G]TCTGTTTGGATCTGG | 23092 |
| rs60795239 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876747 | GAACCATTGCACTCC[A/G]GCCTGGGCAACAGAG | 23092 |
| rs60821175 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882040 | AGTTTCTATTTCCAA[A/G]TTTGAGGAAATTATT | 23092 |
| rs60873577 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997596 | TTTTTTTTTTTTTTT[-/TT]AGTAGAGACAAGGTC | 23092 |
| rs60882886 | snp | C/T | 0.209135 | 0.246638 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951012 | TTCTCTTTCCCTTTC[C/T]CTTTCCCTTTCTCTT | 23092 |
| rs60889944 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911562 | GTTTAAGTGATATCC[A/G]CGTCCCCCACTTTTT | 23092 |
| rs60891090 | in-del | -/TCAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876572 | CTTGAGCCTGGGAGT[-/TCAA]GACCAGTCTGGAGGC | 23092 |
| rs60905948 | snp | G/T | 0.454784 | 0.1434 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080247 | GTCTTAGAGCTTAAA[G/T]TTAAATTGAGGCAAG | 23092 |
| rs60940468 | snp | A/G | 0.198014 | 0.244535 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194666 | GGTTTTGAAGGACAA[A/G]AACTAGAAGAGAATA | 23092 |
| rs60985630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863173 | TGGAGTGCTATGGCA[C/T]GATCTCGGCTCACTG | 23092 |
| rs60996619 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092447 | GGGATTACAGGCGTG[A/G]GCCACTGCACCCGGC | 23092 |
| rs61027802 | snp | A/G | 0.142272 | 0.225598 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180147 | TTGTTTTGTTTTGAG[A/G]TGGAGTTGCACTCTG | 23092 |
| rs61095248 | snp | A/G | 0.152001 | 0.229992 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867756 | CTTCCTCAATGGACA[A/G]CATGAAGGGAGGTGG | 23092 |
| rs61108358 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157577 | ATACGTTGACCATAG[C/T]ACATGATTTCTACAG | 23092 |
| rs61130977 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071006 | AAAAGACCGTGAATA[A/G]CAAAAGCAGTCCTAA | 23092 |
| rs61222912 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181182 | TTGTTCTACCATGCA[A/C]GCTTGAACACAGCAC | 23092 |
| rs61255687 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092443 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 23092 |
| rs61259621 | snp | C/T | 0.133093 | 0.220981 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066486 | TCTTAGAAGAGTGCC[C/T]GGCACATAATACACC | 23092 |
| rs61287676 | snp | A/G | 0.106633 | 0.204807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107853 | TGGTAGCAGAATTCA[A/G]TGAGTTTCCAGCTTT | 23092 |
| rs61349814 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004038 | AAAAAAAAAAAAAAA[-/A]GGAAAGTGACGTACG | 23092 |
| rs61469217 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208195 | TTTGGGAAAAAAAAA[-/A]GAGCTCTTTACAACC | 23092 |
| rs61502472 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115378 | GAAAGAAAAGACGTA[C/T]TATTATGATTTGGGG | 23092 |
| rs61522982 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127774 | ACAAAATGTACATTA[A/G]TTAATATAGTTGGTT | 23092 |
| rs61561102 | snp | A/C | 0.122411 | 0.214991 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973074 | TTTAGATTGGTAATT[A/C]CCCCTAGTCCAGTTG | 23092 |
| rs61610880 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025976 | AACAATGAAAAAAAA[-/A]TAGATGCCTTTGTAT | 23092 |
| rs61656898 | in-del | -/AAATAGCCATA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202486 | ATGAAAATAGCCATA[-/AAATAGCCATA]CTGCCCAAAGTAATT | 23092 |
| rs61662259 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917586 | TTCAGAAAGTCCTCC[C/T]GTGACTAAATTAAAA | 23092 |
| rs61663792 | in-del | -/AA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876801 | AAAAAAAAAAAAAAA[-/AA]GGATTTCTTTAAAAC | 23092 |
| rs61689235 | in-del | -/GTG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012580 | TATATATATATTATG[-/GTG]ATCAGGTTCACCTTA | 23092 |
| rs61697081 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950994 | TTCCCTTCCTCTTTC[C/T]CTTTCTCTTTCCCTT | 23092 |
| rs61711290 | snp | A/G | 0.189261 | 0.242509 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788623 | ATTATTCCCTTAACA[A/G]TACAGTACAACAACT | 23092 |
| rs61749638 | snp | C/T | 0.0016488 | 0.028665 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143147340 | CATGAACTCCAGTGA[C/T]CCAGACCTGGCTGTG | 23092 |
| rs62374604 | snp | A/C | 0.110519 | 0.207473 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052746 | ATGAGTATTTGGCCT[A/C]TTTCTATTTGGATGA | 23092 |
| rs62374605 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075496 | TACCATAGTAGGGAC[A/G]TTTGGTTTTTGTATA | 23092 |
| rs62374624 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081576 | CCAGAAAATTACCTA[C/T]CATCCGAAGACGGTG | 23092 |
| rs62374625 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092963 | GGAGGAACCATCTAT[C/T]GTCCTGTCCTGAAGG | 23092 |
| rs62374626 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116591 | TGACAGCCTGGGGGT[C/T]TCTGCCTTACAAGCC | 23092 |
| rs62376069 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133256 | AATAAAACCTAAATG[A/C]TAACAGTGGTTATCT | 23092 |
| rs62376070 | snp | C/G | 0.181659 | 0.240478 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163500 | CTGTTGCCCAGGCTC[C/G]AGTGCAATGGTGCGA | 23092 |
| rs62376071 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169731 | AAGGCACACGGACTC[G/T]GCGGATGGAGAAGGG | 23092 |
| rs62376072 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191937 | TGTACCGTTTTATGA[C/T]ATCAGATAATTCTGA | 23092 |
| rs62376103 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212852 | GAGAGCTTTTTTAAA[A/T]TACTGATGCCTGGCC | 23092 |
| rs62376104 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222275 | CACACACACACACAC[A/C]CACACACACCCCACA | 23092 |
| rs62382764 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006338 | TTTTTTTTTTTTTTT[A/T]AATTGCAGTTTCTCT | 23092 |
| rs62382767 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031590 | TTTTTTTTTTTTTTA[A/T]TAGCTGGGAGGAGCC | 23092 |
| rs62383265 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768998 | GGATTACAGGTGTGA[A/G/T]CCACCATGCTCCATT | 23092 |
| rs62383266 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777646 | TTCGTTCAGGAAATA[C/T]GGAGACCCTGCTCTG | 23092 |
| rs62383267 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788996 | TTAAGTGTCTTAGAC[A/C]ACTAAAAAGTGCTGT | 23092 |
| rs62383268 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794513 | TGAAAATTACTTTGG[A/G]CGATCAGGCTGTGGT | 23092 |
| rs62383269 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806169 | ACAAAGACGGCTCAC[C/T]GGAGCCTTGACCTTC | 23092 |
| rs62383270 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809375 | GACTTTGAGCTTCTT[A/G]GAAGAAGGGGTCAGA | 23092 |
| rs62383271 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849155 | AGGGATGGGAGTCAA[G/T]GTCAGCAGTTTTGAC | 23092 |
| rs62383272 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851114 | TTTTTTTTTTTTTTC[C/T]TGAGACAGAGTCTCA | 23092 |
| rs62383273 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893939 | AATGGTATTATTTGT[G/T]GGTTTTTTTTTTTTC | 23092 |
| rs62383286 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915813 | TTCTGTTTTTTTTCC[C/T]TCAATATTTAGAAGG | 23092 |
| rs62383287 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920180 | GAGAGGATTTAGTGT[A/T]AAATTTCTGGGTTAA | 23092 |
| rs62383288 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936106 | TGTAGAAAATCCCAA[C/G]GAACACACACACACA | 23092 |
| rs62383289 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946460 | TTTTTTTTTCTTTGT[G/T]GGAAATGCAATTTGC | 23092 |
| rs62383325 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962973 | TCCACTCTCAAGTAG[G/T]CTCCAGTGTCTGTTG | 23092 |
| rs62383326 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974221 | TTTTTTTTTTTTTAA[A/T]TATCTGAATAATTCA | 23092 |
| rs62794561 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822240 | GCAGTTTAGTCTTAA[-/C]TTTGCTCAGAGTGCT | 23092 |
| rs66463225 | in-del | -/ACAC | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222281 | CACACACACACACAC[-/ACAC]CCCACACACACATCT | 23092 |
| rs66480874 | in-del | -/T/TA | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928248 | AAGGCAATGAGTTTT[-/T/TA]AAAAAAAAAAAAAAA | 23092 |
| rs66521053 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214859 | ATGTGGGCGTCTGAG[C/T]CTGCATTCCCTTTTA | 23092 |
| rs66542758 | snp | A/T | 0.436976 | 0.165952 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853196 | TTTAATTTTATTATT[A/T]TTTTTTGAGACAGGG | 23092 |
| rs66608674 | snp | A/G | 0.353587 | 0.22753 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193540 | CAGGCGTGAGCCACC[A/G]TGCCCCGGCCTACAG | 23092 |
| rs66767211 | snp | A/G | 0.215747 | 0.247642 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970552 | CATACTTCTTCCCCT[A/G]TTGTTCCAATAGAAG | 23092 |
| rs66790725 | in-del | -/GAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115359 | ACAACAACAAAAAAC[-/GAAA]GAAAGAAAAGACGTA | 23092 |
| rs66938169 | in-del | -/ACACACACACACACACACACACACACACATAT | 0 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963199 | CACACACACACACAC[lengthTooLong]ATATATATATATATA | 23092 |
| rs66941766 | in-del | G/TGT | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955126 | TGTGCAGAGATGGGG[G/TGT]GTGTGTGTGTGTGTG | 23092 |
| rs66972670 | snp | A/G | 0.189576 | 0.242588 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869233 | TTTTTTTGAGACAGC[A/G]TCTCACACTGTCGCC | 23092 |
| rs67054994 | in-del | -/AAAAAAA | 0.375 | 0.216506 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866042 | GGGGCTTCCAAAAAA[-/AAAAAAA]GAAAAAAGAAAAAGA | 23092 |
| rs67151250 | snp | C/T | 0.239902 | 0.249796 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787866 | GTATCATTAACTACT[C/T]TCTAAGATGGTTTTT | 23092 |
| rs67257383 | multinucleotide-polymorphism | CAT/TAG | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899966 | GATTTATCCTTCACT[CAT/TAG]AGTAAACAGAGCCTC | 23092 |
| rs67285333 | multinucleotide-polymorphism | AAAA/GGGG | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190032 | GGACAGAAGGAGGGG[AAAA/GGGG]AAAAAAAAAAAAAGA | 23092 |
| rs67285334 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190035 | CAGAAGGAGGGGGGG[-/G]AAAAAAAAAAAAAGA | 23092 |
| rs67333369 | in-del | -/TG | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806474 | TTATAGGCAATGAAA[-/TG]TGTGTGTGTGTGTGT | 23092 |
| rs67423184 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893947 | ATTTGTGGGTTTTTT[-/T]TTTTTTCTGTTGAGT | 23092 |
| rs67462099 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132862 | AAAGGAATCTGGGGT[-/A]AAAAAAAAAAAAAAA | 23092 |
| rs67677895 | in-del | -/G | 0.472147 | 0.114677 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949232 | GAGAGGAGAGAGAGA[-/G]GAGAGAGAGAGAGAG | 23092 |
| rs67682062 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886722 | AAAAACCTAAAAAAT[-/A]AAAAAAAAAAATCTT | 23092 |
| rs67688642 | snp | A/G | 0.17461 | 0.238362 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775413 | ATCTTCTTTGGTGAG[A/G]GGTCTTCAGATCTTT | 23092 |
| rs67881734 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993842 | CTTTTCTTTTCTTTT[C/T]TTTTTTTAAGTAGAG | 23092 |
| rs67922441 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941064 | TGGGCGACTGAGAGC[A/G]ACTCCATCTCAAAAA | 23092 |
| rs68003115 | multinucleotide-polymorphism | CT/TC | 0 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869208 | TTCTTTTTCTTTTTT[CT/TC]TTTTTTTTTTTTTTT | 23092 |
| rs70991779 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786655 | AAAAAAAAAAAAAAA[-/A]TTCTAGAACTCCAGA | 23092 |
| rs70991780 | in-del | -/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807962 | AGGCGTGAGCCACCA[-/C]CACCCTGCCAAAATA | 23092 |
| rs70991781 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861362 | TCTGGAAGAAAAAAG[-/A]AAAAAAAAAAAACGG | 23092 |
| rs70991782 | in-del | -/ACACACACACACACACACACAC | 0 | 0 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867307 | GCAAAAACAAACAAA[-/ACACACACACACACACACACAC]ACACACACACACACA | 23092 |
| rs70991783 | in-del | -/AAGT | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880724 | AGCAAAATCCACACA[-/AAGT]AAGAGGGTGGTGTTG | 23092 |
| rs70991784 | in-del | -/G | 0.465052 | 0.127485 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889960 | TTAATAGAGATGGGG[-/G]TTTCTCCACGTTGGT | 23092 |
| rs70991785 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890197 | ATGCAATGCACTTTC[-/A]TATATATATATATAT | 23092 |
| rs70991787 | in-del | -/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936149 | CTACTAATTATAGAA[-/G]GGGGTGTGTGTGTGT | 23092 |
| rs70991788 | in-del | -/C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941100 | ATGGAATATAGATTC[-/C/T]TTTTTTTTTTTTTTT | 23092 |
| rs70991789 | in-del | -/CTCTCTCTCTCTCTCTCTCTC | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949201 | TCTCTCTCTCTCTCT[-/CTCTCTCTCTCTCTCTCTCTC]CTCTCTCTCTCTCTC | 23092 |
| rs70991792 | in-del | -/A | 0.0670745 | 0.170406 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092170 | GGGAGACTCCGTCTC[-/A]AAAAAAAAAAAAACA | 23092 |
| rs70991793 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106480 | TTGAGACATCACCTC[-/A]AAAAAAAAAAAAAAA | 23092 |
| rs70991796 | in-del | -/AA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161026 | AAGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 23092 |
| rs70991797 | in-del | -/AAAC | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163464 | GACTCCATCTTAAAA[-/AAAC]AAACAAACAAACAAA | 23092 |
| rs70991799 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183074 | TGAGGATTTTTTTTC[-/T]TTTTTTTTTTTTTTT | 23092 |
| rs70991800 | in-del | -/G | 0 | 0 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193244 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAT | 23092 |
| rs71276308 | in-del | -/GT | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162312 | GGGAAAGGGGATTGC[-/GT]GTGTGTGTGTGTGTG | 23092 |
| rs71276311 | in-del | -/C/CT/TCTC | 0.75 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949199 | TCTCTCTCTCTCTCT[-/C/CT/TCTC]CTCTCTCTCTCTCTC | 23092 |
| rs71576155 | in-del | -/TT | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785991 | TATTTTTTTTTTTTT[-/TT]AAATAGACAGAGTCT | 23092 |
| rs71576156 | in-del | -/T/TTTTTT | 0.286825 | 0.247273 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787995 | ATTATTAACCAATTC[-/T/TTTTTT]TTTTTTTTTTTTTTT | 23092 |
| rs71576157 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821301 | CCTAAGGTAGAGTGG[-/TT]TTTTTTTTTTTTTTT | 23092 |
| rs71576158 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949221 | GAGAGAGAGAGAGAG[-/A]GAGAGAGAGAGGAGA | 23092 |
| rs71576162 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082018 | AAAAAAAAAAAAAAA[-/A]TGGTAGCTTTTGTCT | 23092 |
| rs71576164 | in-del | -/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163611 | TGCACCACCACACCC[-/C]AGCTAATTTTTGTAT | 23092 |
| rs71576165 | in-del | -/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175838 | GCACAATAGGCCAGG[-/G]CACAGTGGCTCACGC | 23092 |
| rs71576166 | in-del | -/GAAG | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221941 | AAGGAAGGAAGGAAG[-/GAAG]GAAGGATGGAAGGAT | 23092 |
| rs71576167 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221968 | GAAGGATGGATACAT[G/T]TATGGATGGACCAGG | 23092 |
| rs71587236 | snp | C/T | 0.375 | 0.216506 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775461 | GTTATTTCTCTTTGT[C/T]GAGGTTTGTTTGTTG | 23092 |
| rs71587237 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807661 | TGTTGATACATTCCC[A/G]GAATGTTCAAGTTCA | 23092 |
| rs71587238 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815276 | AAACTCCTGACCTTA[A/G]GTGATCTGCATGCCT | 23092 |
| rs71590916 | snp | A/G | 0.115088 | 0.210473 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817313 | GCAAGGGACAGTGGC[A/G]AGTGCCACCTTCACA | 23092 |
| rs71590917 | snp | G/T | 0.118584 | 0.212673 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823223 | CTCGTGCTAAACACA[G/T]GAGCATTTAATTCTC | 23092 |
| rs71590918 | snp | A/C/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830093 | TTAAGTCATTTCCCT[A/C/G]GAATGTTGGCCAAGC | 23092 |
| rs71590919 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836301 | GGAGCTGGCTTCCTT[A/T]AAGCCTGACAGCTTT | 23092 |
| rs71590920 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844054 | AGCTAAAAGTGAGTT[G/T]TTTTTTTTTTTTTTT | 23092 |
| rs71590921 | snp | C/G/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848876 | GGCAGCTCTTTCTTT[C/G/T]CCGCCTACTTGGTTT | 23092 |
| rs71590922 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871986 | TGGGAGGGCAGTCCA[A/G]GAGCAGGAGCTGCAG | 23092 |
| rs71590923 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903170 | TCATGGCAGCTGGAG[A/G]AATGAACGCCTAGGT | 23092 |
| rs71590924 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951016 | CTTTCCCTTTCCCTT[C/T]CCCTTCCCCTTCCCC | 23092 |
| rs71590925 | snp | C/T | 0.030278 | 0.119257 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971308 | TAAATAAAACTAGCA[C/T]GCTTTTGAAGAGAAT | 23092 |
| rs71590926 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977873 | GTGTTTCTCTGTTCG[G/T]ACCACTACTGCTTTC | 23092 |
| rs71590928 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013902 | CACACACTTAAGAAC[A/G]GCTAAAGTAAATACT | 23092 |
| rs71590929 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016198 | AAATTAGGCTATAGA[A/C]CAACATACATAATAA | 23092 |
| rs71590930 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046748 | TATACTTGTTCAGTG[G/T]ATGTCTATCTCTCTT | 23092 |
| rs71590931 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097313 | TTGTACCACTGTACT[C/T]TGCACTCCAGCCTGG | 23092 |
| rs71590932 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097558 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23092 |
| rs71590933 | snp | A/T | 0.0788843 | 0.182262 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124835 | TATCTCTGCAGGGGA[A/T]CTATGGTACCCAGCA | 23092 |
| rs71590934 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167301 | GTTGAAACCTCATCT[C/T]TACTTTAAAAAAAAA | 23092 |
| rs71590935 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167601 | TTCATCAATGATGTA[A/G]ATTGTGTATCACAAT | 23092 |
| rs71590936 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167630 | ATTCCTTAAGACCTA[A/G]AGATGGTAATAGTAT | 23092 |
| rs71590937 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167747 | TTGTCTTGCCTACCA[A/G]AATATCCAGCAGCCG | 23092 |
| rs71590938 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181779 | GGATTTTTTGTTTTG[G/T]TTTTGTTTTTTAATT | 23092 |
| rs71592149 | snp | A/G | 0.122411 | 0.214991 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973323 | TTCTATGTGATGCAG[A/G]TCTGTGTGTCCTTTT | 23092 |
| rs71592151 | snp | C/G | 0.148661 | 0.22854 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139796 | CCAAGTTTCCACACA[C/G]ATACACCATCCAGCA | 23092 |
| rs71614924 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067031 | GGAGGGGGAGGGGCA[G/T]AGGAGGGGGAGGGGG | 23092 |
| rs71741022 | in-del | -/T | 0.461148 | 0.133852 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211579 | TATTTACCTACTTAC[-/T]TTTTTTTTTTTTTTG | 23092 |
| rs71796008 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917058 | TTTTTTTTTTTTTTT[-/T]AGATGGAGTCTTGCT | 23092 |
| rs71821935 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974217 | TCAGTTTTTTTTTTT[-/TT]AAATATCTGAATAAT | 23092 |
| rs71847924 | in-del | -/TTTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087659 | TTTTTTTTTTTTTTT[-/TTTT]TTTGAGACGGAGTTT | 23092 |
| rs71890315 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796055 | ACTAAGGTGTTTTTC[-/TG]TGTGTGTGTGTGTGT | 23092 |
| rs71992474 | in-del | -/TAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105386 | ATCTCAAAAATAAAT[-/TAAA]AAATAAATAAATAAA | 23092 |
| rs72045077 | in-del | -/TT | 0.499104 | 0.0211472 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062520 | ATGTTGTAGCTTGGG[-/TT]TTTTTTTTTTTTTTT | 23092 |
| rs72108928 | in-del | -/AAAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820451 | TTAAAAAAACAAAAA[-/AAAC]AACAAACAAAAAAAA | 23092 |
| rs72141550 | in-del | -/GT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858115 | AGAGAGAGAGAGGGA[-/GT]GTGTGTGTGTGTGTG | 23092 |
| rs72182999 | in-del | -/TACAATG | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867353 | TTTGCTAGTACAATG[-/TACAATG]CCAGGAGTCTGGGCT | 23092 |
| rs72213383 | in-del | -/AC | 0.199679 | 0.244883 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123965 | GTAATAGAAACACAC[-/AC]ACACACACACAAACA | 23092 |
| rs72277170 | in-del | -/GAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958923 | AAAAAAAAAAARARA[-/GAA]AAAAAAAAGAAAGGA | 23092 |
| rs72399054 | in-del | -/ACACACACACAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222247 | CCAAGCTTCCTTCAT[-/ACACACACACAC]ACACACACACACACA | 23092 |
| rs72796649 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774954 | ATATTCTGTTATCTA[C/G]ATGTGCCATAGTTTA | 23092 |
| rs72796653 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795627 | TTCCAGCCCCAAATT[C/T]CCTCCGTATCCACTT | 23092 |
| rs72799069 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859339 | CGTGCCCAGGACTGG[A/G]TACTTAATCTGTGGG | 23092 |
| rs72799070 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886306 | AAGTTCATATGAGGA[C/T]AGTAGAGTCAGAGGT | 23092 |
| rs72799071 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902218 | GTGGTTCTGAGTTAG[A/G]CCATCATCCTCTTCT | 23092 |
| rs72799072 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906654 | GTCCAAGATACAGTG[C/G]TTTGGGAATCTTTGT | 23092 |
| rs72799075 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934452 | TCCTAAAGAGAGAGA[G/T]AAATATAGACAAATG | 23092 |
| rs72799076 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936676 | ACAGAGGGATAGACA[C/T]GTAGATCAATGGAAC | 23092 |
| rs72799077 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938366 | GTCACTGTTGCAACT[C/T]CATAAGCTTTTGTTT | 23092 |
| rs72799079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954255 | GAGAATTTTTTGTAA[C/T]GTTCACTCAATGCAG | 23092 |
| rs72799084 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992397 | AAGATGATTTAAGAA[A/G]TGCAGCAGTGATTTT | 23092 |
| rs72799089 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001623 | TGTTCTGGCTGGCCT[A/C]AGTCACACTATTCCT | 23092 |
| rs72799090 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002535 | ATCCACTTTTTAATG[A/T]TGCATCAGCCTGAAG | 23092 |
| rs72799099 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022985 | GGGCCATCCCATATT[C/T]CTTCTTAGTGCACCA | 23092 |
| rs72799970 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128753 | TCCCACATTACTAGG[A/G]ACCCTGGTACATTTG | 23092 |
| rs72799971 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131267 | GTTACTCTTTTTTGT[G/T]TCTCCAGCATTTACT | 23092 |
| rs72799976 | snp | A/T | 0.131723 | 0.220251 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144992 | TGCCAGGTTTCTGGG[A/T]TTTCTTGTCATATGG | 23092 |
| rs72799980 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149882 | TTCACTCCTTTATTT[C/T]ACTATTTTTCATAAT | 23092 |
| rs72799981 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150821 | AAACTGTAAAACCTC[C/T]AGAAGATAACATAGG | 23092 |
| rs72799982 | snp | C/T | 0.177503 | 0.239258 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152120 | AGGGTATTTTTTTCG[C/T]GGTGAGACTATTCTG | 23092 |
| rs72799988 | snp | C/G | 0.21695 | 0.247806 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156873 | ACTTTCCATCTCCCC[C/G]CAAAAGCCCAGTCAG | 23092 |
| rs72799989 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162298 | ATACACACACACACA[C/T]ACACACACACACACG | 23092 |
| rs72799992 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170892 | TTCTTCTTTTTCTTG[C/G]CCTCCATTCTCTGGT | 23092 |
| rs72799993 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175676 | GGGGTGTGGGAATTA[C/T]TGTTTGTTTAGTATT | 23092 |
| rs72800001 | snp | C/T | 0.188316 | 0.242271 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197268 | CAAGGGAATGGTATC[C/T]TCACCTTTGCTAGAT | 23092 |
| rs72801205 | snp | A/C | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036251 | CTTGTCCACTGTCCT[A/C]AGAAGGTCAAAGATG | 23092 |
| rs72801208 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043278 | CATTTCAAGATTATT[A/G]TTTAAATGGAATTAT | 23092 |
| rs72801212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065288 | TGGATAAATTGATTC[A/G]CTCACACTGTTTTGG | 23092 |
| rs72801219 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098436 | AAAACCAGTTCTTGG[A/G]AATAATTAGTATGGG | 23092 |
| rs73284442 | snp | A/T | 0.18325 | 0.240924 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782495 | GGGCATGGGACATTT[A/T]AAAAACTCCCCAGGT | 23092 |
| rs73286416 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790749 | TCTTACTGTTCCTCT[A/G]GAATGCCTTTGCTAC | 23092 |
| rs73286421 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794268 | ATAATCCCTGAAGCC[A/G]ACCTGACCCAGCCCC | 23092 |
| rs73286423 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824710 | TGCAGCTGTGTCTCT[A/G]TGGGACTTAAGAACA | 23092 |
| rs73286427 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837678 | TGAAATCAGTATTGA[A/G]TATTTCGTAAGATCC | 23092 |
| rs73286454 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864730 | GCATCCCTGTCCTCT[C/G]TCTTCCAGAACATGT | 23092 |
| rs73286462 | snp | A/G | 0.152001 | 0.229992 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868177 | GTTTGGCCTGATTAG[A/G]GAAGTCAGGGAAGGC | 23092 |
| rs73286468 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871093 | TACTGACTCCATACC[A/G]GCAGTCATTACCTAA | 23092 |
| rs73286481 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875333 | TGAAGGCTTTTGTAA[A/C]TATTAAAGGATTACT | 23092 |
| rs73286489 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882289 | TTATGAAGAAGAAGT[C/G]AGTGAACTCCTATCA | 23092 |
| rs73288116 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109124 | ATTAATATTGGTGCT[A/G]ATCATGGGTGGCTAT | 23092 |
| rs73288119 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110318 | ATCTCCAGCACTTAA[A/G]GCAGTCCCTGGCACA | 23092 |
| rs73288134 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114900 | TGGGCTTTGTATGGT[A/C/G]GGGGAGAACTTGCTG | 23092 |
| rs73288142 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119211 | TGTGGAGAAGCCTGA[C/T]GGGGAAAAATGATCA | 23092 |
| rs73288151 | snp | A/C/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120573 | AAATGTATTAAAGCC[A/C/G]TCAAGAGGTTTTACA | 23092 |
| rs73288412 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889323 | CTTTATATTCTAGTA[A/G]TCTAGTAGGCCAGGC | 23092 |
| rs73288450 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906865 | TGCTAATTCTCTTTA[C/T]GTTTAAACAATTTTT | 23092 |
| rs73288460 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915864 | AAGGCATTTTCATGC[A/G]CTGGGTAGCTGCATC | 23092 |
| rs73290136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145257 | GAGAAATGTGAGCAA[C/T]AGTTATGCTCTTCTG | 23092 |
| rs73290137 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149661 | CAATCACCTGAGACG[A/C]CTTGGGTCTCAGCCT | 23092 |
| rs73290152 | snp | C/T | 0.172351 | 0.237636 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164220 | GGAAAGTTTTGAGAA[C/T]GAGTAGTTCTTTAAA | 23092 |
| rs73290156 | snp | C/G | 0.132409 | 0.220618 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166944 | AAGTTAATAATTGCT[C/G]ATGAGGCAAAGTCCA | 23092 |
| rs73290433 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942557 | ATTTGAAGGAAACAA[C/T]AAATTTAGAAGTTAA | 23092 |
| rs73290498 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945630 | GGCTTGGTTGTGTGT[A/G/T]TGTGTTTGCATTAGC | 23092 |
| rs73290501 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947412 | TGCTGAGATGAATGT[C/T]ATCTTTCTCCTACAG | 23092 |
| rs73292273 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201571 | CTGCCGTTGTCATTT[G/T]TAAGTAACCTACAGC | 23092 |
| rs73294158 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210309 | AAAATCATCAGATCT[C/T]GTGAGACCCATTCAG | 23092 |
| rs73294164 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213368 | TACAGGTGCACGTGT[C/G]TGCTCATGCACACAC | 23092 |
| rs73294320 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980104 | CTGACTTATATTGCC[A/G]TTGATTAGTTTCCCT | 23092 |
| rs73294337 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994499 | CAGAGCTGTGGCCAC[A/G]TGAAGGGTATGCAGT | 23092 |
| rs73298554 | snp | C/T | 0.113685 | 0.209567 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043791 | AGGGTGAAATATGTG[C/T]GTATATGAAAGCTGT | 23092 |
| rs73298556 | snp | C/G | 0.0554779 | 0.157039 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044446 | TTCTTGACCATGTTG[C/G]CAGAAGGCTCCAGCG | 23092 |
| rs73298584 | snp | C/T | 0.117886 | 0.21224 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056742 | AATCCAGCATGAATC[C/T]TCACAGTATTATTAT | 23092 |
| rs73298593 | snp | A/G | 0.0908922 | 0.192833 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068277 | AGCAACCTCAAGGGC[A/G]CTTGTGGTACCTGGC | 23092 |
| rs73298598 | snp | C/T | 0.115438 | 0.210697 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073932 | CAGGACAGTCAATCC[C/T]TGGTTATTCGGAAAC | 23092 |
| rs73298600 | snp | A/C | 0.100231 | 0.200173 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074244 | AAATAATAATAACAA[A/C]CTGTATTATTTTGTG | 23092 |
| rs73300571 | snp | A/G | 0.308908 | 0.242961 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090455 | TACGATAGCTATCTC[A/G]GTCGTGTCATTAGAT | 23092 |
| rs73300580 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096382 | TCATTGCAACAAATA[C/T]TACTGTTTTCCTTAA | 23092 |
| rs73300582 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096622 | TATTATATAAAAGGT[A/G]TGCTAAAGGGTCAGG | 23092 |
| rs73300591 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097997 | GAATTCCAATTTTTA[A/G]AAAGTTGTAGTTCTG | 23092 |
| rs73300598 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099188 | GTTTGATATCTATCT[C/T]TGCAGAAGCTGAGTC | 23092 |
| rs73300601 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099662 | GTGTTATTTAGGATT[C/T]CCATAAGTGAAGTTC | 23092 |
| rs73302478 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105584 | ATGCATCCGGGTAGA[C/T]GTTTGTGTGTGGACA | 23092 |
| rs73795905 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769314 | GCTGGTTCCTAGACA[A/T]AGAGATAATTTATTC | 23092 |
| rs73795909 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783488 | TTCACATTTTTTTTT[C/T]CTTTAAAAACATTCA | 23092 |
| rs73795910 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784809 | TTGCATTCATCTTCA[A/C]GATTAATATTAGCAT | 23092 |
| rs73795922 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787523 | TGAGACGTGGATAAG[A/T]TGGATGGCTTACATC | 23092 |
| rs73795923 | snp | A/G | 0.105569 | 0.204058 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789624 | AAAGTTGCCTTATTT[A/G]TATAATTGTTTGTGT | 23092 |
| rs73795926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816839 | GTTAGTGTGATCAGC[A/T]CTGTGCTCAAGAAGA | 23092 |
| rs73795932 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838744 | CTTGTGTCTAGTAGT[C/T]ATGTTGTGGGATCAA | 23092 |
| rs73796530 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045264 | GCAGCTGCCTCTGCC[A/T]GGAGGACATTACAGA | 23092 |
| rs73796531 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045377 | CCATGATTCTCCCTA[C/T]GAGTTAAATAAGTTT | 23092 |
| rs73796534 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053104 | GGGTTGTCGGACTTT[C/G]AGGCTCTGTGTGGTG | 23092 |
| rs73796535 | snp | A/T | 0.0693013 | 0.172766 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053726 | TTAAAGCAATTTTTT[A/T]AAAAATACAAAAGTA | 23092 |
| rs73796539 | snp | C/G | 0.117537 | 0.212022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057152 | TCTTTCTAGCAGGCT[C/G]GTTGTCATATGTGAC | 23092 |
| rs73796540 | snp | G/T | 0.117537 | 0.212022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057153 | CTTTCTAGCAGGCTG[G/T]TTGTCATATGTGACT | 23092 |
| rs73796547 | snp | A/G | 0.095934 | 0.196885 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063191 | CCCTCACTGACTCCC[A/G]CCGGGAACTCAGAGT | 23092 |
| rs73796549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073826 | TTAAAAAGTTGTAAT[C/T]ATTTTTTAATGAGAG | 23092 |
| rs73796610 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908138 | ACTGATTCAGTCCCA[C/T]TCCCACTTGATACCT | 23092 |
| rs73796612 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922174 | TCAAGAAGAAACTGT[A/G]TTAATTTTAAATTAA | 23092 |
| rs73796675 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935864 | TTGAAACTTGGCCAA[A/G]GGGGGAAATGCCAAG | 23092 |
| rs73796678 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945329 | GCCTGCCACTCACTA[C/T]ACCTATTCTATTCTA | 23092 |
| rs73796679 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945801 | TCAGACCTGGAAATT[A/G]ACACTGATACAATAT | 23092 |
| rs73796680 | snp | A/G | 0.375 | 0.216506 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958920 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAGAAA | 23092 |
| rs73796681 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966877 | TATGGTATGACAACC[C/G]TCTGAATGCTTATAC | 23092 |
| rs73796697 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978766 | TTTTTTTTTTTTTTT[G/T]TAAAAATTGAAAATT | 23092 |
| rs73796700 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003851 | TTATCTAAGGGCGCA[G/T]AGTTCAAAAGTGGTA | 23092 |
| rs73796803 | snp | C/G | 0.255503 | 0.249939 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113961 | GCAGACTTCATTCCC[C/G]TCCTGACTTTGCCCG | 23092 |
| rs73796896 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134650 | AATACCTTACTTGTT[C/T]CAAATACCAGTGTGT | 23092 |
| rs73796897 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142101 | CATCTTTCATGTACT[A/G]TGATCAAAACAACAG | 23092 |
| rs73796898 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142124 | AACAACAGATTGACT[C/T]TACTTTTCACTTTTT | 23092 |
| rs73796899 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147861 | CTTCACATCCTCAAA[C/T]CTTAGCATGACTATG | 23092 |
| rs73796900 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149769 | GATGCAGATGAAAAT[A/G]AAGAACAAAGGTGGG | 23092 |
| rs73796901 | snp | G/T | 0.170408 | 0.236992 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150613 | GGGAGGAGGGAGCTG[G/T]AATTCCTCTGGTACC | 23092 |
| rs73796981 | snp | A/T | 0.0520825 | 0.152737 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188919 | GTTACACAGAAGAAG[A/T]GAAGTCCCTGGGCTG | 23092 |
| rs73796982 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188920 | TTACACAGAAGAAGA[C/G]AAGTCCCTGGGCTGT | 23092 |
| rs73796984 | snp | A/G | 0.0520825 | 0.152737 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190504 | ACAAAGCTGTCCACC[A/G]AGAATTTTATGATCA | 23092 |
| rs73796985 | snp | A/G | 0.0524604 | 0.153226 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190815 | AAATCTTACTACTCA[A/G]TAAGAACATGGTGTC | 23092 |
| rs73796986 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194742 | ACTCTTTTTCTCCAG[C/T]GGAAAGGGTGATTTT | 23092 |
| rs73796989 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197755 | TCTAAAATCTTTATT[C/G]TTTGCCTTTGGCATT | 23092 |
| rs73796990 | snp | A/C | 0.0520825 | 0.152737 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197783 | ATTTAGGTCTATAAT[A/C]CATCTGGAACACATT | 23092 |
| rs73796991 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204989 | GGCCTTGCCTACTAG[A/G]TCATTGTCTGGTGGG | 23092 |
| rs73796994 | snp | C/T | 0.00520357 | 0.0507416 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216237 | GCCACACCGAAGCTC[C/T]GGGCACCTCCACCTC | 23092 |
| rs73798503 | snp | A/G | 0.163236 | 0.234461 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152278 | AGTTGTAACCAGTGT[A/G]TCGCGTTAATGCAAG | 23092 |
| rs73798505 | snp | A/G | 0.321053 | 0.23969 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152281 | TGTAACCAGTGTATC[A/G]CGTTAATGCAAGATG | 23092 |
| rs73799006 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852754 | TGGAACTCTGTCATC[A/G]TGATAACATGATCTC | 23092 |
| rs73799007 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863924 | CCTCCTATCTGCGCA[C/T]CTGCTTGGTGTTGAG | 23092 |
| rs73799010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865676 | GTAGGTGTCTCCAAC[A/G]AAGTTCTGGGCCAGC | 23092 |
| rs73799013 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871965 | GGACCGTGTCATCAC[A/T]GCGTGTGGGAGGGCA | 23092 |
| rs73799014 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874194 | GTTGCTTCACTCTTC[A/G]CCATCACCTGCCTTG | 23092 |
| rs73799015 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874328 | CTCCATTAAATGAGC[A/G]AGAATTGAGAAAGTT | 23092 |
| rs73799019 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881195 | GCAGTGGCTTCCGGG[G/T]GTTATGCAGAGCTTG | 23092 |
| rs73799020 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881512 | CCCCTCATGCATATT[A/C]TATTCTCCTATTCAT | 23092 |
| rs73799021 | snp | C/G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883210 | CAGTGACTCATGTTC[C/G/T]CTGGCCTTTTCTCAC | 23092 |
| rs73799023 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883517 | GGAAATGAGTATGTG[C/T]CAGCTAAAATGGATA | 23092 |
| rs73799025 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892799 | ATCAGTCACCTCGAA[A/C]ATTTATCATTTCTTT | 23092 |
| rs73799027 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895849 | CAAAAAAAGATTACA[A/G]TCGGCTTTGGAACCT | 23092 |
| rs73799514 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026218 | GTGAAAACATGGATT[G/T]TATTTATTCTTTCAG | 23092 |
| rs73799515 | snp | A/C | 0.114036 | 0.209795 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026570 | GAGGTGACGTGAGCT[A/C]CTTGTGTTCTAGGAA | 23092 |
| rs73799517 | snp | A/G | 0.176861 | 0.239062 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031446 | TGATGAAGAAATTGG[A/G]CAAAATTGAGAGGCA | 23092 |
| rs73799523 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038537 | GATTGAGCCATAAGG[A/G]TGTTTACACCGTGGT | 23092 |
| rs73799911 | snp | C/T | 0.234692 | 0.249531 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090705 | GGAGGGCTGTCCCTC[C/T]AGTAAAATGAATGTA | 23092 |
| rs73799913 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102175 | TCTCACAGAGAACCC[A/G]TACAGTGCGCGCCTG | 23092 |
| rs74292667 | snp | C/G | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964588 | AAACAACAACAGCAG[C/G]AAAAAAAACCGATGT | 23092 |
| rs74292668 | snp | A/G | 0.245916 | 0.249967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052144 | CTGTGATAGAACTCT[A/G]TGGAATTTACTGTTC | 23092 |
| rs74292672 | snp | G/T | 0.241053 | 0.24984 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106457 | TCCTTTGGAATACAA[G/T]GCATTGGGCTTTTTT | 23092 |
| rs74292677 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215449 | GTGCAGCCTTCTTCC[A/G]TTTTTTAACGGTTTA | 23092 |
| rs74321934 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222198 | GTTTAAACTTCTAGA[A/G]TGATGTAACTTAATA | 23092 |
| rs74331207 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844411 | TTAGCAGTTTTAAAG[C/T]TTTTTTTTTTTTCTT | 23092 |
| rs74338999 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944668 | CTTTTCTCATGTTTA[C/T]TGGCCGTTTCTATTT | 23092 |
| rs74344283 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227762 | AAAAGTGTTGGATGC[A/T]AAGTAACACCAGGAC | 23092 |
| rs74351748 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989920 | CCAAGACACATAATT[A/G]TCAGATTCACCAACG | 23092 |
| rs74354828 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122203 | TTTCATACATTTGCC[C/T]ACATAGTCTCTGTCC | 23092 |
| rs74356283 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100502 | TTACACCAACATCCC[A/G]TAGATGTGGGATTTA | 23092 |
| rs74356728 | snp | A/C | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155588 | GGTTTCTTTCCCAAG[A/C]ACCAGGGACCCATCG | 23092 |
| rs74357866 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045568 | CCTTCCCCTGAGATG[A/G]CTGGGCCGAGTGAAC | 23092 |
| rs74359612 | snp | C/T | 0.116838 | 0.211584 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841200 | GGCTTCCTACCTTCA[C/T]GTAGGCAGACAAAGA | 23092 |
| rs74382769 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187857 | GCAGGACTTCGTGTT[C/G]TTGCTATGTCTTGCC | 23092 |
| rs74397029 | snp | C/G/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846410 | CTCCCAGGGGAATGT[C/G/T]TTTTGGTGTGGCCCA | 23092 |
| rs74407191 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946162 | TAAAGCCTCTCTGAC[A/G]TATATTCAATCTCAG | 23092 |
| rs74410052 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945291 | TCTACCTGTGCTTCT[A/G]TCTCAGAGAAGAGAT | 23092 |
| rs74413307 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934507 | CTAGGCTTAATTTTG[G/T]CTCCCATTGCTGAAA | 23092 |
| rs74414101 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905741 | ATTATGGTTTTTGCC[A/G]TTAAAAGTAATAGCT | 23092 |
| rs74415635 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152040 | GCAAAATTATGGAAT[C/T]AATAAGAAGATCAGT | 23092 |
| rs74418853 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068298 | GGTACCTGGCATCCT[A/C]CTACATTTCTCTAGG | 23092 |
| rs74428029 | snp | C/T | 0.046775 | 0.145601 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143166151 | TCAATTAAAGAATAA[C/T]ACACGCCCTTCCCCT | 23092 |
| rs74428657 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178708 | AGCTTCACATTTCCT[C/T]ACGATTGCCCCAGGA | 23092 |
| rs74453932 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099487 | ATTGAAAGGATGGAC[A/G]AGATAAAAAATCTAC | 23092 |
| rs74456421 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989921 | CCCAAGACACATAAT[C/T]GTCAGATTCACCAAC | 23092 |
| rs74459912 | snp | A/G | 0.109461 | 0.206758 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050771 | AAAGATGACAGGACC[A/G]GAAGATGATAGACTA | 23092 |
| rs74466917 | snp | C/T | 0.100588 | 0.200439 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780995 | TCCAGCTCCTGTTGA[C/T]GTAGAAGGCTACATT | 23092 |
| rs74485704 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961105 | AGAGTGGCATTCCTT[A/G]AATTAGACCTTATCT | 23092 |
| rs74488324 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133269 | TGCTAACAGTGGTTA[C/T]CTCTAGGTGGTAAAA | 23092 |
| rs74490493 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029997 | GGCATGGGGTCGTTT[G/T]GGGGCATGTCCTAGT | 23092 |
| rs74496342 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970730 | CAAGGTGTTGTTACC[A/C]GAAGTGGGAATGGAT | 23092 |
| rs74507305 | snp | A/C | 0.111224 | 0.207945 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863577 | ATTCATTCATTCCTC[A/C]AATATATATTGAGGT | 23092 |
| rs74509616 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108501 | ACCGTGACAGGACAT[A/G]TAGGTTTGTCAATTC | 23092 |
| rs74512065 | snp | A/G | 0.213333 | 0.247296 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053817 | CTTTCAGCCTTGTTC[A/G]TATAAAAAGTTCATA | 23092 |
| rs74534318 | snp | C/G/T | 0.0174554 | 0.0920832 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981954 | ACATAGAAGAGGCCT[C/G/T]GTGCAGGCTTTCATT | 23092 |
| rs74536216 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001215 | GGAGGTCTGAGGGAA[C/G]TATCTGAGCTGATGT | 23092 |
| rs74536582 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032594 | CAGCTTGGTGGTGAT[A/G]GTGTTCTAAACCTTT | 23092 |
| rs74561598 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812192 | GCAGTTGCTGTAAGG[A/C]TCTTTTTAACCCAGT | 23092 |
| rs74571666 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026013 | GGCTAGGGAAGAAAA[A/G]TCTGACTAGCAGTAT | 23092 |
| rs74573525 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099083 | AGGGCAATAAAACCT[A/C]AACTTTTGAGATTAT | 23092 |
| rs74596044 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074542 | AATACTTCATGACAC[A/G]TGAACATTATATGAA | 23092 |
| rs74597655 | in-del | -/CT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132879 | AAAAAAAAAAAAAAA[-/CT]GTTATCTTCTGAAAT | 23092 |
| rs74599970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993801 | CAGGTGCATGCCATC[A/G]TGCCCAGCTAATTTC | 23092 |
| rs74600590 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804800 | CCCGGGCTGAACAGA[A/T]TTTTTTTTTTAAACT | 23092 |
| rs74602121 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815959 | ACCACCATGCTTATT[G/T]TTTTTTTTTTTTTAA | 23092 |
| rs74602892 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880519 | AAGACTCCATGTCCA[A/C]AAAAAAAAAAATCAC | 23092 |
| rs74608543 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817543 | GGGCTGTTGGTGGCC[C/T]GTGGGTGGGATTGGG | 23092 |
| rs74615623 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997785 | TTGTGGTTTCTTTTG[A/G]TGATTTTGCTAAAGT | 23092 |
| rs74618937 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975174 | GCAAGGAGATGTAGC[A/G]TCTGCTTCCCTTGTG | 23092 |
| rs74628507 | snp | A/G | 0.0098053 | 0.069329 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901928 | TGCCTTTCTTCCTTC[A/G]TTACAGCTGCTGGCC | 23092 |
| rs74649023 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155587 | GGGTTTCTTTCCCAA[A/G]CACCAGGGACCCATC | 23092 |
| rs74658119 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787993 | ATGATTATTAACCAA[A/T]TCTTTTTTTTTTTTT | 23092 |
| rs74659287 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802064 | GGCCGTGAGAGTTGA[A/G]ATGAGAGAAACTATT | 23092 |
| rs74665602 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923965 | CCCCCGGGTTCGTGC[A/C/T]GTTCTCCTGCCTCAG | 23092 |
| rs74671249 | snp | A/G | 0.039522 | 0.134904 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832992 | TTTGAAAAGTATAAT[A/G]TGGAAAATTTGTAAA | 23092 |
| rs74687218 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178875 | CCACTTAACTATATG[A/T]TTTTTTTTTTTTTCC | 23092 |
| rs74688471 | in-del | -/AAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997098 | TAGCTGTTTTCCAAA[-/AAA]CTTTATATATATGCA | 23092 |
| rs74691290 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777634 | CAGAAGAAGAGTTTC[G/T]TTCAGGAAATACGGA | 23092 |
| rs74702486 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843532 | TTTGCACATTTTGCC[G/T]CCTTTTAATCTCAGT | 23092 |
| rs74719160 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142771477 | CGATTCCTTGGAGTA[C/T]TGGCAGCCAGTAATC | 23092 |
| rs74723727 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210924 | GCCGAAAACTACCCC[A/G]GGCCCTCTGTATCCA | 23092 |
| rs74725044 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106012 | AGCAGGACTCCCTGA[A/G]CTGTGTTTCTTCCTC | 23092 |
| rs74725486 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921331 | AAGAACATTTTATGC[A/C]GCTTTTAATACAGTA | 23092 |
| rs74735889 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102245 | CTCTTCTCTTCACTT[C/T]CTGCCTTCCAGGCCT | 23092 |
| rs74748391 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984922 | ACCCCTTCTACTTAT[A/T]AAAAAAAAAAGCGGT | 23092 |
| rs74752082 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907055 | GACTGCATGGCACCT[C/T]CCTCTTGAGGTGACA | 23092 |
| rs74758655 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103041 | TTTTCTTCCCCATGA[A/G]AATTTGTGAAAGATA | 23092 |
| rs74760129 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962598 | CAGGCCTGAATGGTG[A/T]AAGGTTTTTTTTTGG | 23092 |
| rs74781390 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048938 | AAAAAAAAAAAAAAC[C/T]TTACCCAATCTAGAA | 23092 |
| rs74783873 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006337 | TTTTTTTTTTTTTTT[A/T]TAATTGCAGTTTCTC | 23092 |
| rs74790770 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067803 | GGGCACCCTAGGCCT[A/C]AAAAATCAGTTTGTA | 23092 |
| rs74791430 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978631 | TAGAGTTCTCAGTGC[A/G]TTTGAATGAGATAAT | 23092 |
| rs74801671 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010986 | AAGGTTAGTGAATGC[C/T]GGTCAGCATGGATTG | 23092 |
| rs74801894 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097275 | GCTTGAACCTGGGAC[A/G]TGGAGGTTGCAGTGA | 23092 |
| rs74804076 | snp | A/C | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114114 | GTGTAGAAGTACCCA[A/C]CATAAGCATTCAATT | 23092 |
| rs74809949 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779231 | GGTTTACACATTTTT[C/G]TAGCACCTCAGAATG | 23092 |
| rs74833613 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899801 | AAGGAGTCATTTCCC[A/G]TAAAAAAATGGACAA | 23092 |
| rs74840895 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810809 | AGAACAAGTATAATT[C/T]GCCCAAAATAGTAAG | 23092 |
| rs74848340 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068184 | AATAAAATAAAAAAT[A/G]AAAGGAATAAAATTT | 23092 |
| rs74849868 | snp | A/G | 0.0244538 | 0.107838 | intron-variant, synonymous-codon | ARHGAP26 | GRCh38.p7 | 5:142919292 | CGAGGTGATGCACCT[A/G]CAAGCCAATGAACAC | 23092 |
| rs74853574 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908928 | GCCACATGCATTTCT[A/G]TGGAGGTGACCTGTC | 23092 |
| rs74859757 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008631 | AAATTTCCTTATGAA[C/T]CTATTTCCCCAGCAT | 23092 |
| rs74871546 | snp | C/G | 0.0952156 | 0.196321 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790017 | AGGTCTTTATTAATC[C/G]AGTCAACAAATGTTT | 23092 |
| rs74874436 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173833 | TGCACCCTAGGCTTC[C/T]CTATACCTAAAAAAT | 23092 |
| rs74882417 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984539 | AAGAAACAGATCTGT[G/T]CATTCATCTCTCAGT | 23092 |
| rs74894199 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993723 | CACAGCACATTGCAG[C/T]CCCAACCTCTTGGGG | 23092 |
| rs74894836 | snp | A/C | 0.5 | 0 | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142771318 | CTCAGCCTTGAGTGC[A/C]CAACCGTGAGAATGG | 23092 |
| rs74897084 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863106 | TGGTTTTCAAGTGAG[G/T]TTTTTTTTTTTTTTT | 23092 |
| rs74901105 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974332 | GGCAGGAAGGGCTCT[C/G]GTTCTCGATGGTGTA | 23092 |
| rs74934115 | snp | G/T | 0.0696718 | 0.173152 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775468 | CTCTTTGTCGAGGTT[G/T]GTTTGTTGTAAAATA | 23092 |
| rs74936428 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038715 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCTTT | 23092 |
| rs74946676 | snp | C/G | 0.0861826 | 0.188849 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899557 | TTTGATAACCAGGTG[C/G]GACTGCAGCAAGCTC | 23092 |
| rs74964274 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121403 | TTGATTGAGCATTAT[G/T]TGCCAGGAACTGTGT | 23092 |
| rs74964572 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173832 | CTGCACCCTAGGCTT[A/C]CCTATACCTAAAAAA | 23092 |
| rs74966869 | snp | A/G | 0.123452 | 0.215605 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985399 | GTATTGTGCAGTAAT[A/G]TCTTAGGCCTTCATG | 23092 |
| rs74970761 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009574 | CATGGCAGGGGTTTT[G/T]TCATCATCATCATTA | 23092 |
| rs74977124 | snp | C/G | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887162 | AGATCCATTCTCTCC[C/G]TGGTCAAATATTGCA | 23092 |
| rs74986361 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166883 | CCATCCAGTATTTTG[A/G]GAGTAACAGTCATAC | 23092 |
| rs75015715 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105952 | TGATTTTTTTTTTTG[G/T]TCATTTTTATAATGA | 23092 |
| rs75032414 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997766 | ACTTTTTTTTTTTTT[C/T]ATTTTGTGGTTTCTT | 23092 |
| rs75032782 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001088 | TAAAAGAATATATAT[A/G]ATGTAAGTCTGTTTG | 23092 |
| rs75042256 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169746 | TGCGGATGGAGAAGG[A/G]GTGGTCCTCAGAGAA | 23092 |
| rs75051822 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857252 | CACATTCTGAGGTTC[C/T]GGGTAGACATCAATT | 23092 |
| rs75055128 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943201 | TTGCCAAATCTTTAG[A/G]TAAACCTAGGGAATA | 23092 |
| rs75063083 | snp | G/T | 0.00199529 | 0.0315338 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217770 | ACCTCTCACCTGGGC[G/T]CTTCCACTGGCCGCC | 23092 |
| rs75067605 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863677 | GAGTCCAAACCCTTG[C/T]CTTGGAGGGTGTGGT | 23092 |
| rs75069129 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958919 | TAAAAAAAAAAAAAA[A/G]GAAAAAAAAAAAGAA | 23092 |
| rs75083379 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814829 | ACACTGGTTGTTGTG[A/G]CAATCAGATGAGATA | 23092 |
| rs75087664 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777509 | AGCCAGTGGAGGAAT[A/G]CTAACCTAGCAGTCA | 23092 |
| rs75091251 | snp | A/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859987 | CTTACTCAGTCGTAG[A/G]TATAAGACACTTACC | 23092 |
| rs75093635 | snp | A/T | 0.309894 | 0.242719 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054312 | TTAATAGGTAAAAAA[A/T]ATACTTGTCATTTTT | 23092 |
| rs75094417 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933525 | AGTGTATTTCTCTCT[C/T]AGAGCCGAGAAGGGA | 23092 |
| rs75112433 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033622 | TTTTTCAAAACTTTT[A/G]TCGATGTTCAGAGGG | 23092 |
| rs75113682 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936837 | GGAAAAAAAAAAAAA[A/G]CCTTGACTTAAACCT | 23092 |
| rs75116629 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197869 | AGTTAGTCTAGCACC[A/G]TGTATAAAAGAGCAC | 23092 |
| rs75119897 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183867 | GAGAATATAGTAGAA[A/G]GGACTTGGGGAAGGA | 23092 |
| rs75124177 | in-del | -/TTC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997091 | ATGAGCATAGCTGTT[-/TTC]CAAAAAACTTTATAT | 23092 |
| rs75149182 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811427 | TAGAGTAGAAGCTGA[G/T]AGTGTGGGCTCTGGA | 23092 |
| rs75150017 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206826 | CCCACAAGAGTGGAA[A/G]CTGAAGGCTCGCTAT | 23092 |
| rs75158915 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797365 | GATTGATGAATGTTG[C/T]AAGTAGTTTTGTTCA | 23092 |
| rs75178014 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811429 | GAGTAGAAGCTGAGA[G/T]TGTGGGCTCTGGACG | 23092 |
| rs75182529 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801194 | TCCTCTGGGTTTGAG[C/T]TGTGGAATTGCTGTA | 23092 |
| rs75183439 | snp | A/G | 0.213937 | 0.247385 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064268 | CCTACCTGCCTGGCC[A/G]TGTTGTAGGCATTTG | 23092 |
| rs75188187 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169804 | GACCTTTCTTATGGG[A/G]ACTTCGTGAAGGATT | 23092 |
| rs75190259 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129389 | TGGGACTTTTTACAG[A/G]TAAGGTCTCTGAAGG | 23092 |
| rs75202803 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803259 | AAATTTTCAGAATAA[A/G]TATGTCCCAATATAA | 23092 |
| rs75211289 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149165 | CCCAGAGGGACTGTT[C/G]CCTGCCTGGTACAGA | 23092 |
| rs75239101 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849278 | TGTGTTCTCACTCTT[A/G]GGTAAGACAGGTTCT | 23092 |
| rs75259696 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183613 | CTTCCCTGCCCACAC[A/G]TACTGTGAGTTGCCA | 23092 |
| rs75267578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854516 | GTGCTCAATGAAGAG[A/T]TAAAGGATGAATGGG | 23092 |
| rs75273437 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076892 | CTAAGTGCACTGATA[G/T]GTGCTTAGAGTTGTT | 23092 |
| rs75276279 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004890 | GCAATAGAAGAAGAA[G/T]TGGGGATGAGGAATA | 23092 |
| rs75289392 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815547 | TTGCTAAGTGATGAG[A/G]GTCATGGATTCTTAT | 23092 |
| rs75290588 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178888 | TGATTTTTTTTTTTT[C/T]CCAAGGAGTCTCACT | 23092 |
| rs75305010 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891765 | TCTGACTGTGTCATT[A/T]CTAAGGAAAACAGTG | 23092 |
| rs75311150 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796824 | TGTTCCTTCTGCCTG[A/G]TGTCTCTGGTACCAT | 23092 |
| rs75324589 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934779 | GATTTTTTTTTTTTT[G/T]GGAGGGGGTTAATTT | 23092 |
| rs75328516 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829604 | GTATTTATCTCTGTG[A/G]CCTGCTTGCCGCACT | 23092 |
| rs75329923 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035823 | TGCCTGTAATCCCAG[C/T]TACTAGAGAAGCTGA | 23092 |
| rs75344003 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185939 | CTCTAGGCCTGTCTT[C/T]CTAAAGGAGCCATCC | 23092 |
| rs75346312 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121921 | ATCTAATAAAAAATG[C/G]TGTTTCTCTTAAATA | 23092 |
| rs75351618 | in-del | -/AT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154851 | GTGATAATTCATAGC[-/AT]ATTTTTTTTTTTAAA | 23092 |
| rs75353036 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785861 | TTGCTTTCCTCCCTT[C/G]TTTTTCTTTCCCTTC | 23092 |
| rs75358383 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183809 | TCAGCAGTGTCTCTG[C/T]GCCTGTCTCTGTCGT | 23092 |
| rs75363447 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212354 | TTCCCAGCCTCTCAA[A/G]AAAAAAAAAAAAAAA | 23092 |
| rs75375661 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058523 | CTAACCTTCCGTTGA[C/T]TTTGATGGTATGTTC | 23092 |
| rs75384577 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940408 | TATATGGTTGACAAA[A/G]TAATCTATACAACAA | 23092 |
| rs75400461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211537 | TTGAGAAAAAAACAA[A/G]GCCCTTTCTTGGCTT | 23092 |
| rs75408998 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126635 | GATTCTTAATTTGTT[C/T]CTTTTTGCCAGACTT | 23092 |
| rs75416705 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004319 | TTTAGTTTGCTTTAA[C/T]ACAGACCTTAATGCC | 23092 |
| rs75425201 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852706 | AGGAGACAATGGGAA[C/G]GTTCTTTGATCCAGA | 23092 |
| rs75428136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790516 | TTTAGAAGTCATAAA[C/T]CTTATTCCACTCTTT | 23092 |
| rs75448826 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910348 | CACTATTTCCTCAGC[C/T]TTAGGGTGAAGGAAA | 23092 |
| rs75460438 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882445 | CCTGCTCTGTGCCAG[C/T]ACTGTTCTGTGCCCT | 23092 |
| rs75460593 | snp | A/T | 0.0839998 | 0.186933 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228796 | AATCTGTGACTAGAA[A/T]AGACCTTTGTCCCTG | 23092 |
| rs75470142 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950398 | AAACTAGTGGTGGGA[A/T]TTTTTTTTTTTAAGT | 23092 |
| rs75477474 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226490 | CGTCTCAAAGGAAAA[A/G]AAAAAAAAAAAAAAA | 23092 |
| rs75477691 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957656 | ACTGTTTTTATTCTC[C/T]GCTACCGTGTGCCAG | 23092 |
| rs75481953 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064554 | GGGATTCTCAAAGGA[C/G]CTTCTCCAGCTATTT | 23092 |
| rs75484139 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816569 | AGAGGAGTTGAGTCA[G/T]AAGAAATAGGAAGAA | 23092 |
| rs75489537 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817603 | CATCTTTGTTACTCA[C/T]GTTCCCTGACCACAG | 23092 |
| rs75492071 | snp | G/T | 0.031825 | 0.122064 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098181 | TCTTGTTCTACAGCT[G/T]TGCTTGACATATTTG | 23092 |
| rs75503645 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983083 | TGGTGGTGTGGAGGA[A/G]GACAGGTCCCCTGAC | 23092 |
| rs75541643 | in-del | -/TTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853196 | TTAATTTTATTATTA[-/TTT]TTTTTTGAGACAGGG | 23092 |
| rs75554783 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799290 | GTTACAACTCAGACT[A/G]TAAGATCCCCTTAGA | 23092 |
| rs75559619 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159411 | GCCTAAATAAATAGT[A/G]GAGTTGAGTACTATC | 23092 |
| rs75563587 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832319 | AAATGGGGTTATATG[G/T]GTGAGGCCCTGATAT | 23092 |
| rs75566327 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873662 | TCGGAGCTTGGGGCT[A/T]CTCTGGTCTTCTCGA | 23092 |
| rs75569356 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222272 | ACACACACACACACA[A/C]ACACACACACACCCC | 23092 |
| rs75579803 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950928 | AGGTTGGTAGATCTT[C/T]GAGAAGTGAGAATAA | 23092 |
| rs75585175 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188904 | CTAGAGATGTGGCAG[G/T]TTACACAGAAGAAGA | 23092 |
| rs75588388 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918003 | TGACACATAAGTCCT[A/G]CAGAAAACTGTTGTC | 23092 |
| rs75588609 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906922 | TCTCCATAAGCACCT[A/G]AAACTAGTATTGGTT | 23092 |
| rs75594575 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025562 | TGTGTAATTCATTCT[C/T]AGAATGTCCAGATCC | 23092 |
| rs75599377 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011602 | CCCTTCCTCAATAGC[C/T]ACATGAGTAAAATGG | 23092 |
| rs75601443 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998751 | AAAAAGAACAAAAAA[A/G]AAGAAAAAGGAAAAG | 23092 |
| rs75609650 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818231 | GTAAAAAAAAAAAAA[A/T]AGTCACTCTGGTTTA | 23092 |
| rs75618096 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832433 | ATGTGAGTGTAGAGC[C/T]GGAAGGCAAGCCAGG | 23092 |
| rs75621483 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875418 | TTTAAGGTCTTTTCA[G/T]AAGGTGTATGACTTA | 23092 |
| rs75642464 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050435 | AGTGCTGTAAAGCAC[A/G]GAATTATAGTAGCAT | 23092 |
| rs75646501 | snp | G/T | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072356 | GTATGGAGGTTTCTT[G/T]AAAAACTGAAAATAC | 23092 |
| rs75654033 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079643 | AAATATATTTACCTT[A/G]TTCAGGTCTTGGAGC | 23092 |
| rs75662573 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896609 | CTTCCTTCCTTCTTT[C/T]TTGAGAAAAGAAATC | 23092 |
| rs75668842 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151590 | ATGCTATATTATTCA[A/G]TGATTTTAAAAAGTG | 23092 |
| rs75669160 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788606 | GATGTTTTTTCCTTG[A/C]CATTATTCCCTTAAC | 23092 |
| rs75671958 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086828 | AGTTGATATGGAGGG[A/G]GGCCACTGGACATGA | 23092 |
| rs75680391 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936836 | AGGAAAAAAAAAAAA[A/G]GCCTTGACTTAAACC | 23092 |
| rs75685210 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815812 | TTCTTCTTATTTTTT[G/T]GAGACCAGGTCTCAC | 23092 |
| rs75725510 | snp | C/T | 0.106633 | 0.204807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104651 | GTGGAAACAATAAAA[C/T]ATTGGAAACAATCTG | 23092 |
| rs75736082 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851847 | TGACTTTATTTCTGC[A/C]TATTAATTTCACACT | 23092 |
| rs75742510 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819623 | TACCTGAACAGGAAG[A/G]GTAGTCATATATAGG | 23092 |
| rs75783524 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167868 | TTTTTTTAACTCTCT[C/T]TGCCATTCAACAGAT | 23092 |
| rs75785753 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154462 | AATTAATAGTATTAT[C/T]TTGGAGGGCTCCCCC | 23092 |
| rs75796156 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980184 | TGTGGCTCCTTTTAT[G/T]CAGTATAATACCTGT | 23092 |
| rs75798601 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936491 | TTCCTATTAGAATCA[C/T]AGCAAGATTTCTTAT | 23092 |
| rs75800490 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897909 | GGGAAAGAAACCAGC[A/C]AGAAGTCTATTGAAC | 23092 |
| rs75802859 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938774 | CCTTAGCTGTGATTA[C/G]TGGTGTCTTTCTGCA | 23092 |
| rs75808051 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874875 | CAGGAACAGGCAGAT[C/G]TTTTCCTTGAAGAAA | 23092 |
| rs75834081 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857524 | TGCCTCTGGCTCAGG[G/T]TCACCTCGTCCCTCC | 23092 |
| rs75838315 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000492 | GATGAATATTAAAAA[C/T]TTTATGCTGAGTGCA | 23092 |
| rs75839346 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178158 | GTGCATGCCACCATG[C/G]CCGGCTAATTTTTGT | 23092 |
| rs75843424 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020157 | TTCAGTGAATGCCTC[C/T]AGAAGTTCTTGGACT | 23092 |
| rs75843807 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152655 | ACCCTTTGACTTATT[C/T]TGGCCAATAGAATGT | 23092 |
| rs75862471 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222018 | AAGAGTAGGAATCTG[C/T]CACTTCTTTGTAGTT | 23092 |
| rs75862597 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152447 | TTCTTTTGAAGTGTC[A/G]GAAGAGTTGGTTACA | 23092 |
| rs75882742 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013678 | GATAATAACAGCTCC[A/T]GCCCAACAGAATTGT | 23092 |
| rs75894110 | snp | C/T | 0.0528381 | 0.153711 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194233 | AGCAGGAAAATGCTC[C/T]TCATTCAACAACATT | 23092 |
| rs75900378 | snp | C/T | 0.0532157 | 0.154195 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224777 | TTCACCTCCAATTCC[C/T]GTGATCCCAAAAGAA | 23092 |
| rs75902122 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163328 | GCAATTGTAGGCAGG[A/G]TTTCCAATAATTTCC | 23092 |
| rs75902370 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953064 | TGTCATGGAGAGGAT[A/G]TAACTTATAACACCT | 23092 |
| rs75903547 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004692 | TGTCACATCACTGCC[C/G]TTTGAGAATCTGAAG | 23092 |
| rs75926611 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826718 | CCCCATCACCAGGTG[C/T]GATCTAGTTTTCAGC | 23092 |
| rs75936527 | snp | A/T | 0.030278 | 0.119257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809892 | ACAGCATGAATAAGA[A/T]AAGGCCCTTCTCTCA | 23092 |
| rs75946914 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787514 | CATAAACAATGAGAC[A/G]TGGATAAGATGGATG | 23092 |
| rs75953463 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067865 | CAACTGTGGTTAATT[C/T]AAAACATAAAAACAG | 23092 |
| rs75955615 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024221 | GTTTGATGAGACCCT[G/T]GCCCCCAAAGCTATG | 23092 |
| rs75966927 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189435 | CCCACACACCCTCCC[C/T]ACCCAGGCACCTGCT | 23092 |
| rs75992399 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001082 | TAGCTATAAAAGAAT[A/T]TATATGATGTAAGTC | 23092 |
| rs75993342 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216066 | CCATTTTACCATTTT[A/G]TGTTCCTACCTTCTT | 23092 |
| rs76001141 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142771032 | CGGTACACTGGGGGA[C/T]GGGTGTCGACGCCTC | 23092 |
| rs76004702 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844856 | TGAGACTGCGTCTCA[A/C]AAAAAAAAAAAAAAA | 23092 |
| rs76009912 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851112 | TTTTTTTTTTTTTTT[C/T]CCTGAGACAGAGTCT | 23092 |
| rs76010624 | snp | A/G | 0.187053 | 0.241946 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152712 | CAGGCCCAGGCCACA[A/G]TGCCTCACAGCTTTC | 23092 |
| rs76018778 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020410 | ATGGCCCAATTACAT[C/T]GTGTGGGTGTATGTC | 23092 |
| rs76035766 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807511 | GGATTCTGCAGGCCA[G/T]GCTTAGCAAAACCTC | 23092 |
| rs76047082 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912391 | GAAAGCAGATTCAGC[A/G]ATTGCTTGGGGATGT | 23092 |
| rs76062669 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934950 | TAAATCATACTTTTT[A/T]AATACACAGTCATAT | 23092 |
| rs76071293 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102129 | TGAGTGATATAGACA[C/G]CAGGACCGTGAGTAA | 23092 |
| rs76071565 | snp | C/T | 0.128258 | 0.218355 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054396 | CTTATTTATTAGTTC[C/T]ATTTTATGCTGTGCT | 23092 |
| rs76073855 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801625 | GGGTTTTTTTTTTTT[-/TT]AACTGTTACCAAGGA | 23092 |
| rs76075781 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898175 | ATATACACACACACA[C/T]ACACACACACACACA | 23092 |
| rs76083598 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017520 | ATTCATTCATTCTTT[C/T]GTTTCATTTTATTTA | 23092 |
| rs76091169 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160474 | GTTGTTGCTTTTGGT[G/T]GTTTTTTTTTCTTTC | 23092 |
| rs76101848 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177114 | GTATAAATTTAATTG[C/T]GCCTTTCTGCTTCAA | 23092 |
| rs76134582 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132436 | GGAGGGAGGAGACCA[A/G]CTTCAAAGAATAAGA | 23092 |
| rs76134729 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168228 | CTGTAATATTACAAT[A/T]GTTTTGTTTTCTTGT | 23092 |
| rs76149280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812463 | GTGCCTCAGCCACCC[A/G]AGTAGCTGGGATTAC | 23092 |
| rs76152195 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797066 | TAGGTGACACAGTGA[A/G]GAGTCTTTGTTCAGT | 23092 |
| rs76167081 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014851 | GCTGCAAGAGTACAA[A/G]GGAAATCCTGTCACC | 23092 |
| rs76171948 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796960 | GAAGCTCACTAGCTA[C/T]AGCGTGGTGTCAGAA | 23092 |
| rs76179093 | in-del | -/A | 0.268724 | 0.249298 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040422 | TGTGTTTTGGCCCCC[-/A]AGTATTTTATACTGG | 23092 |
| rs76179606 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060698 | TGGTTAGAATAACCC[C/G]GGGCGCTTGTTTACA | 23092 |
| rs76181518 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783998 | GGCAGGCACTGGAGG[C/T]GAGTGCCTCAGCATC | 23092 |
| rs76203576 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821741 | TTTGGTGACAATTTC[C/T]AGTGCCAACTCTGTG | 23092 |
| rs76209509 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082195 | CATAGTGATAATGCC[A/G]TGATTGCTTCAGCCT | 23092 |
| rs76220539 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778944 | CAACCAAGGGATAGA[A/G]AAAAAAAAAAAACTT | 23092 |
| rs76224493 | snp | A/C | 0.0685596 | 0.171987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138980 | GTGGGATGGTTCCCC[A/C]GGAGATGCATTCTTT | 23092 |
| rs76231341 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151317 | ACTCTCACTCATTAC[C/T]GGTGGGAATACAAAG | 23092 |
| rs76245298 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185463 | CATCCCTCCTTTTTT[C/T]CTTTTACCAAAAACG | 23092 |
| rs76249035 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006106 | TTTTGATAGCCTTGA[A/G]TTAAGCCAAATAAGA | 23092 |
| rs76252208 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840499 | GGTTTGTGAACAAGA[C/T]AGCCAAGGTTCTACT | 23092 |
| rs76252752 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811428 | AGAGTAGAAGCTGAG[A/T]GTGTGGGCTCTGGAC | 23092 |
| rs76272712 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220929 | TTCTGTAGCAGTGTC[A/G]GAGCGGAAATGCTTT | 23092 |
| rs76280036 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897219 | AAAAGTATAACCATC[A/G]TAGTGTGCAGATGTT | 23092 |
| rs76292735 | snp | C/T | 0.106278 | 0.204558 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772323 | CCTGAAACATATGAA[C/T]AGACCCTTCCTTTGT | 23092 |
| rs76301525 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117876 | AATTGTTTTAGGCCT[A/G]CTCAGAAACTCTCCT | 23092 |
| rs76330895 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147985 | GTTGTCTAGCCCTCC[A/G]CAGAAACTAGGTCTA | 23092 |
| rs76333893 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127178 | TAGTTTTGGTTCAAC[A/G]TGAAATTTCAGGCTA | 23092 |
| rs76346875 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780413 | TTTAATAAGTATTTC[A/G]TAACAGTGTTTCTGA | 23092 |
| rs76351042 | snp | A/G | 0.375 | 0.216506 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990015 | TGCCTTGCTAGATTG[A/G]GGAAGTTCTCCTGGA | 23092 |
| rs76353277 | snp | A/T | 0.0811548 | 0.184367 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163129 | TAAAAAGAAAAAGAA[A/T]AAGACACTATTCGAG | 23092 |
| rs76370725 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992067 | TTAGGACTTTTTTTT[G/T]TTTTTGAATATTCCC | 23092 |
| rs76372622 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815813 | TCTTCTTATTTTTTT[G/T]AGACCAGGTCTCACT | 23092 |
| rs76389746 | snp | C/G | 0.10237 | 0.201756 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776927 | TCCTCGCCAATACTT[C/G]TTGTTGTCTTTCTTT | 23092 |
| rs76413541 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998532 | TGGTTGCTCAGGTCC[A/G]GTGTGCTTTTGTTCT | 23092 |
| rs76427442 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934952 | AATCATACTTTTTTA[A/G]TACACAGTCATATCC | 23092 |
| rs76432021 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882285 | GTTATTATGAAGAAG[A/G]AGTGAGTGAACTCCT | 23092 |
| rs76434261 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786911 | TGGCCTCCCAAAGTG[C/G]TGAGATTACAGGCAT | 23092 |
| rs76439586 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115362 | ACAACAAAAAACGAA[A/C]GAAAGAAAAGACGTA | 23092 |
| rs76441026 | snp | A/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085261 | CAGTAGGTGCTTCAT[A/T]GAACATCCTCTGGTG | 23092 |
| rs76442802 | snp | A/T | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912642 | CCCAGGAGACAAAAG[A/T]AAGCAAAATTTGACC | 23092 |
| rs76448152 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866618 | TTGGAAAGAGGAGCA[C/T]GTCTTTATTCTACTT | 23092 |
| rs76455460 | snp | A/T | 0.0267878 | 0.112589 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966659 | AATGTATTCCAAGTC[A/T]GTAATTGAGAAGAAG | 23092 |
| rs76475610 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212029 | CCCTGTTTTGTCCCA[G/T]TATCCTTGTTTAGTG | 23092 |
| rs76487206 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214161 | ATAAATAACTGGCAT[C/T]TTCAAAGCTCCTCCC | 23092 |
| rs76492132 | snp | C/T | 0.105924 | 0.204309 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973424 | AGGATGTTTATGAAG[C/T]CTGTGCACATGCTCT | 23092 |
| rs76495449 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100945 | AAAAAATTGAAAAAC[C/T]AGCTGAGTGTGGTGA | 23092 |
| rs76496603 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097822 | ACGAGACTCCAACTC[A/C]AAAAAAAAAAAAAAA | 23092 |
| rs76497232 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176148 | TAAATAAATGAAATA[C/T]GACACGTGACAATGA | 23092 |
| rs76512341 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012537 | ACTGGAGGGATATAT[A/T]TATATACATACATAC | 23092 |
| rs76556046 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015741 | GGGGGAGGAGAGGCA[C/T]GTGAATGGAGACCTC | 23092 |
| rs76559484 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039612 | AAATGGAGCCAAAAG[C/T]GAGTCTAAAAAAAAA | 23092 |
| rs76565435 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812215 | AACCCAGTTCTTTAC[A/G/T]GGAAAACTCACTGTA | 23092 |
| rs76566185 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013629 | GACATTAGTTAACCC[C/T]TCTAGGCTTCATATT | 23092 |
| rs76566830 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937790 | AAAAAGGCCAGTCTC[A/C]AAAAAAAATATACTT | 23092 |
| rs76569531 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997096 | CATAGCTGTTTTCCA[A/T]AAAACTTTATATATA | 23092 |
| rs76600669 | snp | G/T | | | intron-variant, synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143172968 | CCATAGGGTTCATGC[G/T]AGTTCAGCAAGCAGT | 23092 |
| rs76600861 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939678 | TATGGTGGTTAAGAA[C/T]GTGCACTCACACAGC | 23092 |
| rs76602135 | snp | G/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991720 | ACATGCTGTATAGGT[G/T]TATCTCCTAGGAACA | 23092 |
| rs76602257 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789120 | TTCTGTTTTCTCATT[A/T]ACAAAATGGAGACAC | 23092 |
| rs76606311 | snp | A/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157990 | ATAATAATACCTACT[A/T]TCAAGGTTATAAGAT | 23092 |
| rs76607338 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997765 | TACTTTTTTTTTTTT[C/T]CATTTTGTGGTTTCT | 23092 |
| rs76615573 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142859075 | TTGGATTTATTTTGA[G/T]TGGGGTGGGAAGAGT | 23092 |
| rs76616697 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129618 | ACCTTGGACAAATCA[A/G]TGAATCTCAAGGAGT | 23092 |
| rs76620329 | snp | A/G | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962094 | AAGCAGGAGAAATGC[A/G]AGTGGCGAAAAAATG | 23092 |
| rs76623534 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945805 | ACCTGGAAATTAACA[C/T]TGATACAATATTATT | 23092 |
| rs76628414 | snp | C/T | 0.0271762 | 0.113356 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968173 | CTCTATGAGGTAGGT[C/T]GTATTTCCCTCAGTT | 23092 |
| rs76663320 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160476 | TGTTGCTTTTGGTGG[G/T]TTTTTTTTCTTTCTT | 23092 |
| rs76670768 | snp | C/G | 0.196064 | 0.244113 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197322 | GATTGTAGCAATTTA[C/G]ACCCCTCCTGCAGCA | 23092 |
| rs76674890 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126311 | TGTGGGTTGTTAGCA[A/T]GTAGTGGGTGATGAT | 23092 |
| rs76676503 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972588 | AAGATACATATATGT[A/G]GTAAAGCAGTTACTA | 23092 |
| rs76679117 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132287 | TGTTTCCTACACATC[A/G]GCTTTTGAGTTCTGT | 23092 |
| rs76680941 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164514 | TCATCATTTCAAAGA[A/C]TGAGACTCTTTTTGC | 23092 |
| rs76690214 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773060 | GTATTCTACCACTAC[C/T]AACTACTACTTGATC | 23092 |
| rs76704517 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221424 | CAAAATGACAGCAAC[A/C]AAAAAAAAAAAAAAA | 23092 |
| rs76717396 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039529 | CAACAGGAGTTTTAA[A/T]TTTTTTTTTTAAATT | 23092 |
| rs76718142 | snp | A/T | 0.125528 | 0.21681 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876739 | CTGTGATTGAACCAT[A/T]GCACTCCAGCCTGGG | 23092 |
| rs76718759 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985349 | TTTAAATAACTTTAG[C/T]GTAGCCTAAGTGTAC | 23092 |
| rs76722416 | snp | C/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164985 | TTGTATGCTGCCACA[C/G]CCCTATGCTTTGCTT | 23092 |
| rs76723248 | snp | G/T | 0.152334 | 0.230133 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800361 | AAGGCTGAGGTCTTT[G/T]TCTTTGTCTTTTTTT | 23092 |
| rs76733352 | snp | C/T | 0.131723 | 0.220251 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167396 | CTGAGACATGAGAAT[C/T]ACTTGAACCCGGGGG | 23092 |
| rs76738633 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045603 | CATTAACTATTTCTT[C/T]ATTATACATTCATTG | 23092 |
| rs76752703 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993995 | GAATCTAAGATGTGC[A/G]TTGACAACATTTTAG | 23092 |
| rs76754794 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821206 | GGTGAATTACTCACA[C/T]ATGGGCCAAAGTGAT | 23092 |
| rs76755977 | snp | A/G | 0.0337553 | 0.125452 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963940 | ATTAAAGATTAAAAA[A/G]TAACCAGAATTCACG | 23092 |
| rs76756561 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009563 | GATGTCTGGCACATG[A/G]CAGGGGTTTTGTCAT | 23092 |
| rs76760527 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810124 | GGTGAAGAGAAGGCA[A/G]TATTTGGCTGATGAA | 23092 |
| rs76764976 | snp | A/G | 0.172674 | 0.237741 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163233 | GGGAGCATTGCTGCC[A/G]ATGCAAGATACATTT | 23092 |
| rs76782892 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101555 | TTTCCCTCTCCTTTC[C/T]TTAACATCCAACCAG | 23092 |
| rs76784036 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184935 | GCTTATATTTTGACT[C/T]AGCCACTGCACCCCT | 23092 |
| rs76789770 | snp | C/G | 0.0640965 | 0.167152 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816153 | AGCATAGAGATATTG[C/G]TAACTGTACACTCAT | 23092 |
| rs76793483 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839207 | AGTCGTTTGAGTTTA[C/G]TGGGTTTGAGTCTCT | 23092 |
| rs76799167 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948653 | ACTTTCCTTAGCTCT[C/T]TTTTTTTTTTAAGAA | 23092 |
| rs76800666 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217157 | TTTGTGTGTTTCAGG[A/T]TTAAGAAGAATGAAT | 23092 |
| rs76800673 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126312 | GTGGGTTGTTAGCAA[C/G]TAGTGGGTGATGATG | 23092 |
| rs76814169 | snp | A/C | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889711 | ATGAAAGCCTCTCCT[A/C]AAGAGGTAACATTTA | 23092 |
| rs76821520 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110761 | AGTAATTTTCCAGGA[A/G]GAAAGGCTTTCTGAG | 23092 |
| rs76825369 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948451 | AATTTCTTGCCATCT[G/T]CTGGCTTTCTTTGAA | 23092 |
| rs76832821 | snp | A/G | 0.188 | 0.24219 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154503 | CCTTACTTTTTCTCC[A/G]GTCCCTCAGCCATGG | 23092 |
| rs76840405 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805119 | TTCTTTTTTTTTTTT[G/T]TGAGATGGAGTTTCA | 23092 |
| rs76858632 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885925 | TTTTGTGCTTTGGTA[A/G]TGTTGTTTCAAGAAA | 23092 |
| rs76860775 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193786 | TTCATTATATTGTTA[C/T]AATTGTTTTATCATT | 23092 |
| rs76863574 | snp | A/G | 0.00611549 | 0.0549577 | synonymous-codon, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143214060 | TGACTCAGAACTTTC[A/G]TTCACAGCAGGCACG | 23092 |
| rs76866295 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789859 | CTTTCCTTATGTATC[C/T]AGGACCAGGGCACTC | 23092 |
| rs76869088 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144952 | CTTTCTTCTACAAAA[C/T]TGTAGTCGTTTTATA | 23092 |
| rs76878904 | snp | G/T | 0.0825414 | 0.185628 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974442 | GAAAATTACAGGCAA[G/T]GGCCCTCTTTACATG | 23092 |
| rs76889300 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061408 | TGTAGATTTATTACC[A/G]TGTATGCAGTGAGGA | 23092 |
| rs76892635 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942774 | ATTGTGATTGTGGTG[G/T]GTTTTTGTTGTTGTT | 23092 |
| rs76894761 | snp | A/G | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768927 | CGCTGTGTTGCCCAA[A/G]ATGGTCTTGAACTCT | 23092 |
| rs76910075 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132657 | CTGGAATAATTCATA[C/T]AAAGCATTTAACTTA | 23092 |
| rs76910416 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957908 | TTCTCAATCTGCAAA[C/G]GTACTTGAACTGGGC | 23092 |
| rs76910677 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005793 | TTTTATTCACCAGCA[A/G]GAACGCTTCCGGGGC | 23092 |
| rs76916215 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147943 | AGCATTGAGCACCCA[C/T]AGTCAGGACAATTAG | 23092 |
| rs76922282 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054152 | TCAAAGGGTATAAAC[A/G]TTTTTAAGACTTTGA | 23092 |
| rs76924204 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218546 | TGCTCCCTGTCCATG[C/G]TGAGTGAAGGAGGGC | 23092 |
| rs76927615 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861171 | GGAGCCTGGGGATTT[C/T]GTGGGCACCTATGAG | 23092 |
| rs76939797 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886227 | CGTGGCTTCCAGGCC[A/G]GCCCTTTTTTTAAAA | 23092 |
| rs76976733 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171703 | TCCTCCTACATTTGC[A/C]CATTTCTGCCATTAA | 23092 |
| rs76994815 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220077 | GGTGAACAGCTAGCC[A/G]GGAAAAGGAGAAAGG | 23092 |
| rs76994992 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006319 | TTAGTGTTTTTTCTT[G/T]TTTTTTTTTTTTTTT | 23092 |
| rs76998611 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015272 | AGAACACTTGAAGTC[A/G]ACTCTGACTAACTGA | 23092 |
| rs77003549 | snp | C/G | 0.29789 | 0.24537 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813844 | TTAGGGGCCTCAATT[C/G]AGCCCTTGACAGTGT | 23092 |
| rs77003723 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820927 | CAAGATGACTAGCCT[C/T]CTGTCCCTCCACCTC | 23092 |
| rs77021125 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183791 | TGTGAGTCCTGTGGC[C/T]CCTCAGCAGTGTCTC | 23092 |
| rs77028777 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794261 | CCTTGAGATAATCCC[C/T]GAAGCCGACCTGACC | 23092 |
| rs77038604 | snp | C/T | 0.0592355 | 0.161582 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860129 | TTCCTGTCTCCTCTG[C/T]GCACACATGCTCCAC | 23092 |
| rs77044214 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070397 | TATGTTATTAATATA[A/T]AGTGACTCTTGACAT | 23092 |
| rs77047605 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896804 | AAGTTATTTCTCTGA[C/G]CCTTACTTTCCCCAT | 23092 |
| rs77048644 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840497 | GGGGTTTGTGAACAA[C/G]ACAGCCAAGGTTCTA | 23092 |
| rs77049538 | snp | A/C | 0.172028 | 0.23753 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197209 | AGTGTACACATAACA[A/C]ACCTTTCTCTGGGGT | 23092 |
| rs77056093 | snp | C/G | 0.196771 | 0.244268 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151149 | AGGACATACAGGTGT[C/G]AAGTAAGCATATAAA | 23092 |
| rs77066422 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077190 | GCCTCAGGTATGTGG[G/T]CGCCAGTATTTCCCA | 23092 |
| rs77066915 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095103 | GGTTCTAAGATAATA[C/T]ATTCTTACATATATA | 23092 |
| rs77069906 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967722 | ACCAGAAGCATTTAG[C/T]TGGGTAAATAGAAGG | 23092 |
| rs77088209 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906200 | TGCCCCTCAGTGGTG[A/G]TGTAAATTTTGATCA | 23092 |
| rs77104676 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148093 | AATCTTGTCAACTAG[C/T]GCCTTTGCAGAAAGA | 23092 |
| rs77114590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206310 | CACTATTTGTGATGT[A/G]TGATTTCACAGAGTT | 23092 |
| rs77149245 | snp | C/G | 0.000445776 | 0.0149228 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142903632 | CAAGACCATCAGTCC[C/G]TACACCATGGAGGGA | 23092 |
| rs77153832 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911694 | ATTTGGTGATCCTTT[A/G]TATATCCCTATTCCC | 23092 |
| rs77161814 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882441 | AGAGCCTGCTCTGTG[C/T]CAGCACTGTTCTGTG | 23092 |
| rs77186330 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133414 | GCATCACAGATAACA[C/T]GGAGCTGCTGAACTA | 23092 |
| rs77196950 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001087 | ATAAAAGAATATATA[G/T]GATGTAAGTCTGTTT | 23092 |
| rs77197935 | snp | A/G | 0.115438 | 0.210697 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856716 | ACAACGATTTACATA[A/G]CATTTACATTGTATT | 23092 |
| rs77200203 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059021 | TGTTTAAAATAATGG[G/T]AACTGGGCTTTAAAA | 23092 |
| rs77218874 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011658 | GGTCTTAGCTTCTCT[C/T]CAACCCCTTTGTTTG | 23092 |
| rs77220877 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979517 | TCTGGCAAACATAGA[C/T]GTATCTCTTGAGGGC | 23092 |
| rs77226084 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134842 | TAGGAAGTTATGCGA[A/C]TTAAATGAAATTATG | 23092 |
| rs77230183 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801108 | GCTATGTGGTTTTAG[C/T]TGGTTGGAGCACAGG | 23092 |
| rs77243725 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082225 | TTGACACTTGTCCCA[A/C]CCCCCAAGACAATAA | 23092 |
| rs77250192 | snp | C/G | 0.00993419 | 0.0697739 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222788 | AGAAAGAGGAAGTCA[C/G]ATAGAAATAGTCCCT | 23092 |
| rs77257270 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024220 | TGTTTGATGAGACCC[G/T]GGCCCCCAAAGCTAT | 23092 |
| rs77257658 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956795 | CCTCACAATTATGGC[A/G]GAGGGTGAAAGGCAC | 23092 |
| rs77265288 | snp | G/T | 0.030278 | 0.119257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817791 | TGATGGTGGAGAGTG[G/T]TTGTATCAGCATTAT | 23092 |
| rs77283673 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025169 | TCTTTAAAGTTCCTC[C/T]GGGCATTGCCTTATT | 23092 |
| rs77293676 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088444 | GCCATGATGATCATA[A/G]AACTCAGGGGTTTGG | 23092 |
| rs77302670 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172538 | TGAATCTCTATATTA[A/C]TGATTTTGAATAGCT | 23092 |
| rs77303350 | snp | C/T | 0.281528 | 0.248004 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108352 | TTTTTCACCTTTTAC[C/T]GTATGAATTGACCTC | 23092 |
| rs77316838 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985119 | AATGTTTGTGTTTGC[A/G]TCTTGGTTTTTTAAC | 23092 |
| rs77317774 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008671 | GTCCAGATTTTGATC[C/G]AAAGTGTGGTATGGC | 23092 |
| rs77321512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842910 | TTCTTGTGGGACAAA[C/T]TCATGAAAATTATCC | 23092 |
| rs77322034 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170118 | TAGAGAACAAATGGC[A/G]AACACCGGTGTGCTG | 23092 |
| rs77323293 | snp | A/C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806286 | TATTTTTTGTAGAAA[A/C/T]GGAATCTCACTATGT | 23092 |
| rs77332850 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195329 | CAGGGTTACCTGTAA[A/G]CTGAAATGCCTTGGG | 23092 |
| rs77336466 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086316 | TTTTCTAGAATTTTG[A/G]CTGTGGGGGAAATAA | 23092 |
| rs77336616 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903761 | GCCTACCTTACTGTA[A/G]ATACATGCTTGGATA | 23092 |
| rs77337189 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778444 | TTGTCCTTTTTCTGC[A/G]TGTTTTTTTCATAAA | 23092 |
| rs77337572 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916999 | CTGAGGTTCTCAGGA[A/G]CCTGTTCCAGGGCAC | 23092 |
| rs77342998 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805121 | CTTTTTTTTTTTTTT[G/T]AGATGGAGTTTCACC | 23092 |
| rs77347326 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907633 | GAATTATGGGTTGTG[G/T]TTTTTCCAGCTCATG | 23092 |
| rs77356148 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780041 | CACTTCTTCCTCTGG[A/C]GGCATTTTATTGGTT | 23092 |
| rs77399089 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102185 | AACCCGTACAGTGCG[C/T]GCCTGGCTGGGGAGA | 23092 |
| rs77400155 | snp | C/T | 0.140908 | 0.224942 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079190 | TCAGTTTGGAAATGG[C/T]AGAGGGATGGGAGGG | 23092 |
| rs77410138 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, missense | ARHGAP26 | GRCh38.p7 | 5:142919392 | GGAGGAACCCTTGAT[C/T]TTGAACTTTTAGCCT | 23092 |
| rs77442646 | snp | A/G | 0.0505692 | 0.150756 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008565 | TCATAGAGTTTGGAT[A/G]TGCATTTGGGTAAAG | 23092 |
| rs77453584 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951946 | GTGTTGGCAGGGCCA[C/T]GTTCCCTCCAGGGAA | 23092 |
| rs77489172 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030666 | TCTCAGAGGGTTTAT[A/G]TCAGTTGAAATTGAA | 23092 |
| rs77489757 | snp | C/T | 0.0471551 | 0.14613 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970835 | AGGAAGAGGATGTGA[C/T]GGTCACTCTAGAAAG | 23092 |
| rs77506353 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003853 | ATCTAAGGGCGCATA[G/T]TTCAAAAGTGGTAGA | 23092 |
| rs77517434 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821544 | TTTATTGCTGGGCCA[C/T]GGCTGGGAATTATCA | 23092 |
| rs77519018 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900477 | AAGGGCCATATTGTC[A/G]TAATCTGGGTTTTAT | 23092 |
| rs77529614 | snp | A/C | 0.039522 | 0.134904 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189332 | CACTTGGGCTTAAGA[A/C]AGTGAGCCCTCAGCA | 23092 |
| rs77531664 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210598 | TGCTCACCCCTCCCC[A/C]AAAAAAGCCGATAGC | 23092 |
| rs77533971 | snp | A/G | 0.079617 | 0.182947 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146618 | AGCCCATTACAGAGC[A/G]ATTTATCAAAGAATT | 23092 |
| rs77538363 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778596 | TGTGGATATGCCATA[C/G]TTGGTATTTACTCAG | 23092 |
| rs77538438 | snp | A/C/T | 0.0146857 | 0.0845856 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790894 | TCTATCTCATTACCC[A/C/T]GTTTAGTAGTCTTTA | 23092 |
| rs77540246 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809000 | GCCCCTTTTTATAAG[A/G]TAAGTGCCTGTATGG | 23092 |
| rs77541730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083293 | CATACATCGCAGTAA[C/G]CGGCCTAATGATCAG | 23092 |
| rs77545201 | snp | G/T | 0.0715223 | 0.175059 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853938 | GGAACGAATGAAGCT[G/T]TGAGCAGGCCAAGAA | 23092 |
| rs77552961 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896289 | CTTTATATATACTTC[A/G]ATTAATATTATTCCA | 23092 |
| rs77576301 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774539 | TAACATCCTGCATTA[A/G]CATAGTACAGTTGTT | 23092 |
| rs77578848 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890572 | GAAGATATTCTGGCT[C/T]CTGTGTGCAGAGTGG | 23092 |
| rs77593706 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803691 | GCAGTTCACCCTGGA[A/G]CAGTTAGAGGTCAGC | 23092 |
| rs77598190 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935282 | CAGAGTGGTGAGATG[C/T]TTCCTTACTATTCAT | 23092 |
| rs77601594 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923525 | CCCATCAGTGAATAA[C/T]GCCTTGTCCTTGTGC | 23092 |
| rs77615836 | snp | G/T | 0.115788 | 0.21092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831129 | GTCTGTTTCTTTCTT[G/T]CTTTCTGTGGTTCCC | 23092 |
| rs77621399 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205627 | AGTCCTGCTATGTCA[A/G]AGGGAGTACGCTGGC | 23092 |
| rs77626864 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107054 | TACTGATGTATCTGT[A/G]TGTTATTTGCCGTCG | 23092 |
| rs77627403 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991716 | GGTAACATGCTGTAT[A/T]GGTTTATCTCCTAGG | 23092 |
| rs77632858 | snp | G/T | 0.0916144 | 0.193427 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211862 | GCCTAGTTTGTTATT[G/T]TTTAACGTACTATGT | 23092 |
| rs77643113 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148938 | AACTAGTGGTCTGTA[A/G]TTTTCTTTTCAGTGG | 23092 |
| rs77661754 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031588 | TTTTTTTTTTTTTTT[A/T]AATAGCTGGGAGGAG | 23092 |
| rs77666711 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804313 | TTACACATAACTTGC[C/T]GAGGCTGACTAGGGT | 23092 |
| rs77675655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198448 | GAGAGGCTACACTTA[A/G]GTTCAACAGGAAAGA | 23092 |
| rs77703403 | snp | C/T | 0.375 | 0.216506 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989873 | AATGTTAAGGGCAGC[C/T]AGAGAGAAAGGTCGG | 23092 |
| rs77705183 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135409 | TATTATAACTCGTTT[C/T]TGTGAGGTACAGTAA | 23092 |
| rs77707099 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114180 | ATAACCATTCCCAGG[A/G]AGATGTTAAATGTGT | 23092 |
| rs77713773 | snp | C/T | 0.139225 | 0.224118 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803877 | CCTGGTCCTTGATCA[C/T]TGAGGAGTGTATAGT | 23092 |
| rs77717014 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970934 | GCCATCTTTCAGGAC[A/G]TAGGATTCTTTCATA | 23092 |
| rs77725846 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972651 | CAGTTAACCATTCTC[C/T]ACCCCCCAAGAACAG | 23092 |
| rs77730303 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126371 | AAGGGTCCTGAAAAC[C/T]ATAGGAAAAGGTTTT | 23092 |
| rs77741826 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905071 | ATGTAGCTACTTCAG[C/T]TGTGTGTTTTGTATA | 23092 |
| rs77759354 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220990 | AGCCCAGGAAGGGAA[A/T]AGGGGAAAATCTATT | 23092 |
| rs77766318 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114808 | TGGGATTGACCGTGA[C/T]GTATCTCTTAGAGGA | 23092 |
| rs77777956 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783563 | TCAGGATCTGGGGAG[A/G]GGAGGAGAGAGACTG | 23092 |
| rs77819462 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064556 | GATTCTCAAAGGACC[A/T]TCTCCAGCTATTTTT | 23092 |
| rs77822751 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840350 | ATGGAGGAATAATAC[A/G]TTGGTTATTTTTTTC | 23092 |
| rs77827606 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058517 | TGTGTTCTAACCTTC[C/T]GTTGACTTTGATGGT | 23092 |
| rs77839677 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174207 | AATCTATTGTTCAGT[A/G]TTAAGGATCCGGTTG | 23092 |
| rs77846768 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973151 | TGGGCTAGAACAAAT[C/G]CCAGAACTACAGGTA | 23092 |
| rs77847297 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979525 | ACATAGACGTATCTC[C/T]TGAGGGCTAGGAGTG | 23092 |
| rs77849504 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848926 | GACTGTCAGAGGACA[A/C]ACATGGGTGTGTTAG | 23092 |
| rs77850082 | snp | C/T | 0.111224 | 0.207945 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864956 | TGTGTGATATTTGTA[C/T]TTGAGCTGCCTGGAA | 23092 |
| rs77853475 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905674 | GAGTATTTTCTAAGA[A/T]TAAAAGATATTCTTT | 23092 |
| rs77870698 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162966 | CTATTAAAAAAAAAA[A/G]GTTAGCTGAGTGTGG | 23092 |
| rs77872103 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102028 | GGAGCCTGCAGCATG[G/T]TTTTTTTGTAGTAAT | 23092 |
| rs77873398 | snp | G/T | 0.0525012 | 0.153278 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195041 | ACATGTTTAGACTAC[G/T]AAATAAGCACCAGAA | 23092 |
| rs77896271 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205460 | TTTAGAATATGTTGA[A/G]TCTTATTGTGATTCT | 23092 |
| rs77913522 | in-del | -/C | 0.0603597 | 0.1629 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093793 | GAGCTACTCTTTCTT[-/C]CTCTGAGAAGAAAGG | 23092 |
| rs77915904 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923859 | TTAGGATCAGATCCT[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs77917430 | in-del | -/A | 0.300421 | 0.244863 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803994 | GTCATAGTAATCCTT[-/A]ACAGCAGCCCTGTGA | 23092 |
| rs77921866 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778943 | ACAACCAAGGGATAG[A/G]AAAAAAAAAAAAACT | 23092 |
| rs77921975 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159894 | GGAACACTGCCTTTT[C/T]ATTTTAACACTACCC | 23092 |
| rs77931976 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226491 | GTCTCAAAGGAAAAA[A/G]AAAAAAAAAAAAAAA | 23092 |
| rs77932615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858296 | TCTTTTATCATTTGC[C/T]TAGTGGCAAAGTGGT | 23092 |
| rs77936057 | snp | G/T | 0.0486741 | 0.148216 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791840 | ATGGTGGCACGCGCC[G/T]GTAGTTCCAGCTATC | 23092 |
| rs77946574 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102131 | AGTGATATAGACAGC[A/G]GGACCGTGAGTAAGG | 23092 |
| rs77946854 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178898 | TTTTTTCCAAGGAGT[C/T]TCACTCTATCACCCA | 23092 |
| rs77949467 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132501 | TCAATATATAGTGGG[A/G]GTGTTATGCAGCCAT | 23092 |
| rs77954292 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803064 | TGTCATAAAGTATGG[A/G]AACCTTATCTTTCTG | 23092 |
| rs77955364 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812379 | CTCTTTTTTTTTTTT[G/T]ACAGAGGAGTGTAGT | 23092 |
| rs77962048 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868256 | ATGTGGTGGCAGGTA[A/G]GAGTTGGGCATGCCC | 23092 |
| rs77970351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030530 | CTAGGTGGCATGCCT[A/G]TATTGATACAGGAAG | 23092 |
| rs77988459 | snp | C/T | 0.0215218 | 0.101478 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056004 | TTATTATTAAGCTGA[C/T]TAGCCTATCTCCTTT | 23092 |
| rs77997209 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840496 | AGGGGTTTGTGAACA[A/C]GACAGCCAAGGTTCT | 23092 |
| rs78014518 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177751 | TGGCATACTGTACTA[A/T]AGTTGCCCATTTTCT | 23092 |
| rs78017767 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810986 | TGAATAAATCTACCC[C/G]CTTCCAGTCCTTTCC | 23092 |
| rs78020438 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175933 | AGCCTGGCAAACATG[C/G]TGAAACCCCTTCTCT | 23092 |
| rs78026899 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882264 | TAATAAAACTTGCCT[C/T]GTAGAGTTATTATGA | 23092 |
| rs78049623 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227859 | ATGCTTACTGAGGAG[A/G]AAAAAAAAAGCGATC | 23092 |
| rs78058122 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785198 | GCCTCCCAAAGTGCC[A/G]GGATTCCTTAGGATT | 23092 |
| rs78058772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914917 | AAGTACAGCCACCTG[G/T]GATGCTCATCAAATG | 23092 |
| rs78071775 | snp | G/T | 0.0607341 | 0.163335 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966598 | GCCATGAAAGACTTT[G/T]TTGTTTATTTAATAG | 23092 |
| rs78091336 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957909 | TCTCAATCTGCAAAC[A/G]TACTTGAACTGGGCA | 23092 |
| rs78107458 | snp | A/C | 0.241053 | 0.24984 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985968 | GCCGCAATAAACATA[A/C]GTGTGTATGTGTTTT | 23092 |
| rs78112827 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898005 | AGGGACCTCTATGCA[A/G]ATCGACCGTGTTCAT | 23092 |
| rs78118756 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912107 | ACAGAAACCCTAACA[A/G]ATTCCTAAGTGACAG | 23092 |
| rs78120786 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211014 | TTTTTATTTTATTTT[C/T]TTATCAGAGCCAAAG | 23092 |
| rs78122023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142859037 | GTGGGGTGTGCAGAC[A/G]AGGTAGATTTTGTAG | 23092 |
| rs78132217 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840498 | GGGTTTGTGAACAAG[A/C]CAGCCAAGGTTCTAC | 23092 |
| rs78147773 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118340 | CTTCTTCTTTTTTTT[A/G]AAGATGAGGAACCCA | 23092 |
| rs78165592 | snp | A/T | 0.0685596 | 0.171987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835415 | TGCAATCTTTATCAA[A/T]GTGAAATAGTCAAGG | 23092 |
| rs78178247 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220455 | TTCATATTTGCAAGA[A/G]CCCAGTAAAGGGAAG | 23092 |
| rs78182761 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876316 | CAAGATGCATTTTCT[A/G]TTTTAACCCCCATGA | 23092 |
| rs78192964 | snp | A/T | 0.0763149 | 0.179815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997706 | AGAGGTGGGAGATAC[A/T]GCACCTAGCCCAATA | 23092 |
| rs78194221 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022640 | TTTTTAAAATTAGTC[G/T]AAATGGGATGGCATG | 23092 |
| rs78197492 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801390 | TGTCATTCAGTCATC[A/G]GAACTTTATAATGTA | 23092 |
| rs78211674 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126310 | CTGTGGGTTGTTAGC[A/G]AGTAGTGGGTGATGA | 23092 |
| rs78214892 | snp | C/G | 0.341501 | 0.232653 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795107 | CATTCCTAACTCACA[C/G]GTCATACAAACACAA | 23092 |
| rs78220310 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177327 | TCAAATGAAGGAATC[A/G]GCTTCTCAGGCTGCA | 23092 |
| rs78220836 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077733 | AAATGTCTGACTGTT[C/G]TGAGCAATTTCTAAA | 23092 |
| rs78228644 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957834 | GCGCTCTCTCTTTTT[C/G]TCTCTTACCCCTTCC | 23092 |
| rs78242151 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998400 | TGTGCGTTCATCTGT[C/T]ATGCTCTCAAGACAG | 23092 |
| rs78247602 | snp | A/T | 0.0528381 | 0.153711 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935320 | TTACATCTTATTATT[A/T]AAAACATGGGTCAGT | 23092 |
| rs78252289 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828498 | ATTTAAAAGAAAAAC[A/G]TGGAGAAGGAAATTA | 23092 |
| rs78267734 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105950 | AGTGATTTTTTTTTT[G/T]GGTCATTTTTATAAT | 23092 |
| rs78270006 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939451 | CGTCTTTGTGGACTT[C/T]GGGGCTGAACAAAAT | 23092 |
| rs78270877 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905789 | CTTGCCATTAAAAGT[A/C]ATGGCTAAAATCGCA | 23092 |
| rs78275762 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818635 | GAGTCTTCATTTCCT[C/T]ATGTATAAAATGAGG | 23092 |
| rs78278066 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133347 | AATTGTCCATAGTAC[A/G]TGTGTGGGTGTGTGT | 23092 |
| rs78292831 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014524 | ACGGTCTCGCTCAAA[A/G]GACTGGAGAGGCAAT | 23092 |
| rs78305987 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062031 | GAGGATTGGATATCA[A/G]AATAAAGGCAGAGCT | 23092 |
| rs78313723 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076041 | CTCTCACTCTGTCAC[C/G]CAGGCTGGAATACAG | 23092 |
| rs78322458 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198662 | AGTGAGAAAAGATTC[A/G]GATTATTGACTTGGG | 23092 |
| rs78323251 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902332 | TCAGGATTTCCTTTG[A/G]CGGTGGAAATCCCAG | 23092 |
| rs78328071 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212372 | AAAAAAAAAAAAAAA[A/T]TGCCTCTTATATTCC | 23092 |
| rs78334573 | in-del | -/AGTAACTG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039341 | CCTCCTGAGTAACTG[-/AGTAACTG]GCATTACAGGCGCCT | 23092 |
| rs78342603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884122 | AGCAAATTTGATCCC[A/G]TTTATCAGCCAAGTG | 23092 |
| rs78358791 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073398 | GCATCTCTGATTAAG[C/G]TGGCTCAGACTGAGC | 23092 |
| rs78375105 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169066 | AAAGTGACTGTTGGG[A/G]CCTTTGCTTTTGCAA | 23092 |
| rs78383543 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189406 | GTTGCCCTAGCCACA[G/T]AATCCAAATTACACC | 23092 |
| rs78393627 | snp | A/T | 0.14933 | 0.228835 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795057 | CTTCTTCTTTTTTTT[A/T]AAAAAAATTTATAGC | 23092 |
| rs78411527 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834990 | AGACTCTGTTCCACC[A/T]GGTTCACGTGTGAAC | 23092 |
| rs78412167 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891457 | CTTTCGGGGTGTTTT[A/C]TAACATAATGTGTTT | 23092 |
| rs78414514 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145811 | GGGGCTTTATCTAGG[A/G]CATTAAGGATTTGCT | 23092 |
| rs78421437 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957156 | GAGTGATTTGAATCA[A/G]AAGAATGAGGATGGA | 23092 |
| rs78421530 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997097 | ATAGCTGTTTTCCAA[A/G]AAACTTTATATATAT | 23092 |
| rs78426208 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867860 | GTCCTAACTTACCTG[C/T]TTTTTTTTTCACATG | 23092 |
| rs78429185 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809633 | GGAGTCCCATTATTT[A/G]TACAGTTGCTAGCTT | 23092 |
| rs78439501 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928234 | TTGTGTGTGTGTGTT[G/T]TTTTTTTTTTTTTTA | 23092 |
| rs78440174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026608 | AAGAACAGTGGTGCC[C/T]GGATGGGAGGAGGCC | 23092 |
| rs78444006 | snp | C/T | 0.326976 | 0.237854 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027542 | CTTACTGGTTTTAAA[C/T]CAATTCATCCATTTT | 23092 |
| rs78445257 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962611 | TGAAAGGTTTTTTTT[G/T]GGTTGTTTACTTGTT | 23092 |
| rs78448109 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050360 | CTTCTTTTTTTTTTT[-/TT]AAACCACATTTAAAG | 23092 |
| rs78450620 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794178 | ATTGGTGGGATGACT[C/T]GGCCAAGATTTTGAA | 23092 |
| rs78454473 | snp | A/G | 0.107694 | 0.205546 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862298 | GTAGAACTTATAGAC[A/G]TTGAGTTTTCCATTC | 23092 |
| rs78466069 | snp | C/G | 0.0607341 | 0.163335 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105698 | GGCATCTGTCTGCAT[C/G]TCTGAAAATGCCACG | 23092 |
| rs78473051 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806536 | GGTTGTTGAAATTCC[A/C]AAATCTGGGGACTAC | 23092 |
| rs78475688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150241 | TTAGCAACTGTGGCT[A/G]AACCTATTTTATGCC | 23092 |
| rs78501271 | snp | C/T | 0.125874 | 0.217008 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880094 | CAACCTGGAGATCAC[C/T]GTTTGTTATCACTGA | 23092 |
| rs78512891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205268 | GGGACCTTGGCAAAT[A/G]TCATTTATTGTATTG | 23092 |
| rs78525582 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154374 | GTAAAATAGTGTGAT[C/T]ATAACCTCCTCAAAT | 23092 |
| rs78527286 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105676 | GCACTGTGTTCCTGG[C/T]GGGAGTGGCATCTGT | 23092 |
| rs78528446 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096830 | CCCCTGAAGGGTGTT[A/G]GAAACCTCCCCGTAG | 23092 |
| rs78535024 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922031 | AAATACAGGTGCATT[C/T]GGGTTATATGTGCAA | 23092 |
| rs78537179 | snp | C/G | 0.030665 | 0.119967 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861256 | TCCCCTGAGGTATAG[C/G]AGAAAAGTGACTAAT | 23092 |
| rs78565198 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975284 | GGACTAGAGAACTGC[A/G]TCTACAGTAGTGATT | 23092 |
| rs78571813 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206375 | AAAGGGCTAACACAA[C/T]CAATTAAAATCCACA | 23092 |
| rs78576774 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846043 | ATTTTGTGCACCGCA[C/G]TGAAACTGGCTACCT | 23092 |
| rs78582191 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015790 | GTTTACTTTTAACTT[A/G]TGACCTTATGAACCT | 23092 |
| rs78583368 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874047 | GTTGGCTGAGCTATG[C/T]GTCTGCCACTGCCTT | 23092 |
| rs78587073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165396 | ATGGACTTTCTTGTA[C/T]ACGGTGCATAATGTG | 23092 |
| rs78593726 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775496 | ATATACATAACACAA[C/T]GGTTACCACTTTAGT | 23092 |
| rs78598378 | snp | C/G | 0.0718919 | 0.175435 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184302 | AATATTCAGGCCTCC[C/G]CCTAACCTGAATTAA | 23092 |
| rs78614390 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182685 | ACAATTGATTTTTAT[A/G]TACTCATAGCCCTGA | 23092 |
| rs78621882 | snp | A/G | 0.124837 | 0.216412 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871211 | CCAGTGGACAAGGAA[A/G]TCAGGTCACCTGCTG | 23092 |
| rs78628087 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164924 | ATATAATCAGTGTGT[C/T]GGGCCTCAAAAGAGA | 23092 |
| rs78629028 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140494 | CAGTATATATAAAGT[A/G]CTTGACATTGGGCCT | 23092 |
| rs78631158 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101339 | TTCACTTTCAGTGCT[A/G]GGGACCAACAGGTCT | 23092 |
| rs78637848 | snp | C/G | 0.031825 | 0.122064 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925656 | ACTCTTCTTGCAAGT[C/G]GATGGCAGCTGATGC | 23092 |
| rs78649786 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163330 | AATTGTAGGCAGGGT[C/T]TCCAATAATTTCCCT | 23092 |
| rs78654192 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178159 | TGCATGCCACCATGC[C/T]CGGCTAATTTTTGTA | 23092 |
| rs78661332 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098025 | CTGCCTTGGAATCTT[C/T]TCAGAATTCCATACA | 23092 |
| rs78669622 | snp | A/G | 0.02016 | 0.0983543 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069472 | TTGTGAATCTGCTGC[A/G]GGTTAACATTCCTAG | 23092 |
| rs78675696 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191933 | GAGCTGTACCGTTTT[A/C]TGACATCAGATAATT | 23092 |
| rs78677163 | snp | C/G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213424 | GTCTATTCCCTCCCC[C/G/T]GGGGGTTGGAGAGCT | 23092 |
| rs78689620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864629 | GGTAATTAAGATTCT[C/T]CTTTGGTTGATTCTC | 23092 |
| rs78700460 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178890 | ATTTTTTTTTTTTTC[C/T]AAGGAGTCTCACTCT | 23092 |
| rs78702923 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206462 | CCGTCAAGGAACAAA[A/G]TGAACAAATTGAAGG | 23092 |
| rs78719557 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924559 | GTTAGCACATAATAA[A/C]CACTCAGTAAATCTA | 23092 |
| rs78741455 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812378 | CCTCTTTTTTTTTTT[G/T]GACAGAGGAGTGTAG | 23092 |
| rs78751685 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129283 | CCAGTTATTTCCCTT[A/C]TTGTGTGTCTCCTTT | 23092 |
| rs78763341 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100505 | CACCAACATCCCGTA[A/G]ATGTGGGATTTACAA | 23092 |
| rs78764418 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216856 | CACTTTCTCAATTGG[A/G]TTAGCTCAAAATATG | 23092 |
| rs78780040 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984540 | AGAAACAGATCTGTG[C/T]ATTCATCTCTCAGTG | 23092 |
| rs78792241 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936444 | TAGTAAAGATGTCAA[G/T]TCTCCCCAAAGTGAT | 23092 |
| rs78795251 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031128 | AGCATGGTTAGTTGA[A/C]TGTTCTTGAAAGACA | 23092 |
| rs78795545 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013948 | ATTGAATGGGTTCAT[A/G]TTTGGGAGCCAGAAA | 23092 |
| rs78798867 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906962 | TGCAGGCTGACTAAT[A/G]CCTTCTTCCTTTAAT | 23092 |
| rs78802686 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776553 | GTGTTTGAGGCTCAT[C/T]GTGTTGTAGCATGTA | 23092 |
| rs78826490 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222273 | CACACACACACACAC[A/C]CACACACACACCCCA | 23092 |
| rs78840653 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921153 | CCCAACCTAGCATTT[C/T]ACATCCACTGTCAAC | 23092 |
| rs78845401 | in-del | -/TA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976659 | AAAAGATATTTTTTT[-/TA]ACATGCCAAAAATAC | 23092 |
| rs78846184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997902 | TGAACTTTGTTCAAG[C/G]ATAAATTATAATGCA | 23092 |
| rs78859980 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146735 | AGTCGTAAGGACATT[A/G]GTGGCTAAATAGTAG | 23092 |
| rs78881628 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006497 | TGGGAAGTGCCATCA[A/G]CTATATTTTTATTGG | 23092 |
| rs78888476 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927896 | TGTGGTTTTAATCAC[A/G]TTTCCCTCATAAGTA | 23092 |
| rs78902576 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781242 | AGGGTACCTCTGTTA[C/T]TTTTGCCCCACCTCA | 23092 |
| rs78925358 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840816 | GCTAGATTAAGCAAC[A/C]CTTCCATATCTACTC | 23092 |
| rs78932435 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852378 | CATTGCTGAGTTCTT[C/T]ACTAGTGCTGGCTAA | 23092 |
| rs78940562 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863330 | GCCAGGCTGGTCTTG[A/G]ACTCCTGACCTCGTG | 23092 |
| rs78940713 | snp | A/G | 0.125528 | 0.21681 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780214 | ATTGCATTGTATTCT[A/G]TTGTATGAATTAAAT | 23092 |
| rs78950172 | snp | A/T | 0.0603597 | 0.1629 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109043 | GGATCTGGTTTCAGA[A/T]GACTGCTGTTTATTT | 23092 |
| rs78956095 | snp | A/G | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192286 | GGGCTTTGAGTGGCG[A/G]ATGAGCAGTGGTTAC | 23092 |
| rs78962621 | snp | A/C/G | 0.0543475 | 0.155628 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228385 | CACAAGAGAGGCTGT[A/C/G]GATGGCCTATTAAAA | 23092 |
| rs78964652 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848049 | CAGTTGTTCAATCCA[A/G]TTGAATGGCAGTGTC | 23092 |
| rs78967852 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868427 | GGTATTGACACAACT[A/G]GGTGGAGAACTGATT | 23092 |
| rs78971228 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070913 | CTTGACACTATCGCA[A/G]AAAAAAAAACAACAA | 23092 |
| rs78976485 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853808 | TGAGTCCACACTGGC[A/T]GGAGGCTACAAGCTT | 23092 |
| rs78979879 | snp | C/G | 0.0799831 | 0.183287 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146713 | GGTCAGGAATTTAGA[C/G]TGGTGGAGTCGTAAG | 23092 |
| rs78991591 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935330 | TTATTAAAAACATGG[G/T]TCAGTAACCTTTTTC | 23092 |
| rs79020874 | snp | A/C | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887406 | CTACTTATGTTATAC[A/C]TGAGAAGGCAAATAT | 23092 |
| rs79035689 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015846 | CAATAGATTTGAAGG[A/G]CAACCATGGTTCTAG | 23092 |
| rs79037913 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012402 | TGACCAGCCATTCTC[C/T]GTCATATTTCTTAAG | 23092 |
| rs79042882 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140338 | GCAGTCAGACTGAGA[A/T]GTTTTAATGTCATCT | 23092 |
| rs79059056 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143208640 | ACTAAATGAGAGCCA[A/G]TCCAGAATTCAGGAC | 23092 |
| rs79067280 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910354 | TTCCTCAGCTTTAGG[A/G]TGAAGGAAATATGAG | 23092 |
| rs79070308 | snp | C/G | 0.0811548 | 0.184367 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198545 | CTGACCCTTTCCCTT[C/G]AGGTTTTTCTGTACA | 23092 |
| rs79074406 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862732 | TTTGTCCTGAATTCC[A/G]TTTATTGGCAAGGCC | 23092 |
| rs79094425 | in-del | -/AAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048934 | GAAAAAAAAAAAAAA[-/AAA]CCTTACCCAATCTAG | 23092 |
| rs79095015 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916724 | ATTTCTGGTCTCTGA[A/G]ACAGATTACTTGACC | 23092 |
| rs79095189 | snp | C/T | 0.120674 | 0.21395 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878406 | GCAGCCAATCAAGAA[C/T]TAATCCATTCATTCA | 23092 |
| rs79097406 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926923 | ACACTTTGAAATGCC[A/G]CATACACTTCTCATA | 23092 |
| rs79102884 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776809 | TGTTTAAGTTTAATT[C/T]AAACTTGTGTTTATT | 23092 |
| rs79108842 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865887 | CTGCTTTTTCTGGGT[A/G]GGTTCTGCATTTCGC | 23092 |
| rs79124534 | snp | G/T | 0.0232847 | 0.105357 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227817 | ATCCTAAGGAGCTTT[G/T]GATACTTTTTTAGAA | 23092 |
| rs79126871 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195221 | CTTAATCATCCTGGA[C/T]ATTGTCCTTGCAGAA | 23092 |
| rs79128277 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898177 | ATACACACACACATA[C/T]ACACACACACACACA | 23092 |
| rs79130633 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061773 | TCCTGCTCAGCCAGC[A/G]TCTTGTGTTGGCTAG | 23092 |
| rs79135501 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019270 | TGTTTCTTCTTAAGC[C/T]TTTTTTTTTGAGGAA | 23092 |
| rs79138482 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118944 | TAAAAGTATAATAAT[A/T]AAAAAAAAAAAAGAA | 23092 |
| rs79156081 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827113 | CTTCTGTTTTTTTTT[-/TT]AAATCCTATTTTTTT | 23092 |
| rs79170492 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841924 | CCTCTCTTGTGAGCT[C/G]TGCTCTTGGTTTAGG | 23092 |
| rs79173497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954833 | TTTTTCTTTGTTTAG[A/G]AATGTGCAGTATACC | 23092 |
| rs79178223 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196053 | AGGTACTTACTGTTC[A/G]TATGTTTTAAGATAG | 23092 |
| rs79179963 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992129 | AATTAGTTTATCCTT[C/T]GTACATTTTTTTTCT | 23092 |
| rs79184079 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973338 | GTCTGTGTGTCCTTT[A/T]AAGAAAAGCACTGTG | 23092 |
| rs79184836 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046460 | GTACTGATCAGGATT[C/T]CTTAAGAAAGCTTGC | 23092 |
| rs79185896 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102130 | GAGTGATATAGACAG[A/C]AGGACCGTGAGTAAG | 23092 |
| rs79199045 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016022 | TAAATTTGTTGGGGC[A/G]TTGGTGATAATAGCA | 23092 |
| rs79208980 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008658 | GCATCTTTATTTTGT[C/G]CAGATTTTGATCCAA | 23092 |
| rs79211537 | snp | C/G | 0.0832709 | 0.186283 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865812 | GGCATACAGGTCCTT[C/G]CATGGTTTGATTCTA | 23092 |
| rs79250424 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167136 | TGATATATTCTGTCT[A/T]TGAAGGTAGAAAAAT | 23092 |
| rs79252204 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143058309 | GTTACATGCATTAAA[A/G]CCTTTGAAGAAGTAT | 23092 |
| rs79264172 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118110 | ACAGAAAGGAATGGG[A/C]CATTTGAGCTGAGCC | 23092 |
| rs79267974 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774675 | AATGACATATAAACA[C/T]CATCATAGTAACATA | 23092 |
| rs79274557 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897148 | CTAGTCAAGATAGCA[A/G]GCAGTTCAGTGACAG | 23092 |
| rs79280768 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835796 | TGGTTAGCCACCAAC[A/G]CCAAGAGATGGATAA | 23092 |
| rs79311241 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001089 | AAAAGAATATATATG[A/C]TGTAAGTCTGTTTGT | 23092 |
| rs79320283 | snp | C/G | 0.0663309 | 0.169604 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080627 | CCCTGGGCGTGGTCA[C/G]GGAACAGTAAGATCT | 23092 |
| rs79327659 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166766 | TGAACTGGGTTACCA[A/G]CCTTTCAGCAGGAAC | 23092 |
| rs79344774 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923763 | AGACTATTATTATTG[C/G]TATGATCCTAATTAT | 23092 |
| rs79350054 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012051 | AGATGAAGTTACCAA[C/T]GGGGAAGCCCAGGCC | 23092 |
| rs79352209 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947264 | CAAACTAAGGAAATC[A/G]TCAACATTCTTGGGG | 23092 |
| rs79352592 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855414 | ACTTAAGGAGGCTCT[C/T]GTATCTTTTGCACTT | 23092 |
| rs79362932 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078231 | ACCAAAATGATGTGT[C/T]AGCAGGGCTGGGCCT | 23092 |
| rs79387184 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097821 | AACGAGACTCCAACT[A/C]AAAAAAAAAAAAAAA | 23092 |
| rs79395813 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903251 | GCTTATCGTAAAACA[C/T]ACTTTTTGGCATCCA | 23092 |
| rs79397871 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818230 | TGTAAAAAAAAAAAA[A/G]AAGTCACTCTGGTTT | 23092 |
| rs79410613 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824988 | AATGAAAATGGATCA[A/G]CAACTCTTTTCATTC | 23092 |
| rs79415907 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786011 | TAGACAGAGTCTTGT[C/T]TTGTCACCCAGTGTG | 23092 |
| rs79443505 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984709 | ATGGAGCTAAAAAAT[A/T]CCTATCTCTTAGTGC | 23092 |
| rs79443686 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083075 | TAATACAGCAGTCGA[A/G]GGCAGTCTCTATGTA | 23092 |
| rs79448481 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162575 | GCATTATCCCAAGAG[A/T]AGACTACAAACATTT | 23092 |
| rs79451134 | snp | A/G | 0.106278 | 0.204558 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106164 | CTGGTACATAGCAAC[A/G]GGATTGTGGTGTGGC | 23092 |
| rs79456981 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178157 | GGTGCATGCCACCAT[G/T]CCCGGCTAATTTTTG | 23092 |
| rs79461622 | snp | A/C | 0.135143 | 0.222054 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773555 | ATCCCGTAAAGGAGA[A/C]ACATGCAGCAGGTGC | 23092 |
| rs79475527 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212373 | AAAAAAAAAAAAAAA[A/T]GCCTCTTATATTCCT | 23092 |
| rs79479832 | snp | A/C | 0.311123 | 0.242413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097445 | AGTACATTCAGGTAA[A/C]TTTACCTAATTCTAT | 23092 |
| rs79491693 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855526 | TTGACTGCCTGTTAT[A/G]CACTAGGCCTATATC | 23092 |
| rs79495897 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794378 | ATAAATACAGAAGGA[C/G]GGGGGACAGAGGCCA | 23092 |
| rs79497754 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913800 | CCAGGAAAGACACCA[A/G]ACCACTCGTGAAATC | 23092 |
| rs79499365 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786669 | ATTTTTTTTTTTTTT[C/T]TTTTTTTTTTGAGAT | 23092 |
| rs79500802 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984931 | CTTATWAAAAAAAAA[-/A]AGCGGTCAGACAGCC | 23092 |
| rs79503222 | snp | A/G | 0.0014816 | 0.0271773 | synonymous-codon, intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207255 | GCCCATGTTCTCGGC[A/G]CCATCCAGCCCTATG | 23092 |
| rs79504133 | snp | A/G | 0.101658 | 0.201233 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778735 | AGATGGATTCCTTCA[A/G]GTGGAATGGTTGCTG | 23092 |
| rs79517572 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003002 | TATCCTGATTTGAGG[C/T]TGAATTTTTCTTAAG | 23092 |
| rs79522923 | snp | A/G | 0.0654984 | 0.168698 | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142771109 | TGAAGAGAGAGACCC[A/G]TCGCTCCGCCTTTTG | 23092 |
| rs79527602 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957131 | TGATGACTTGATGGG[C/T]ACTTGAAAAGAGTGA | 23092 |
| rs79533287 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213572 | TTCTTTTTGACTCAC[G/T]GAGCATTGCCAGCTT | 23092 |
| rs79554021 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838953 | ACTTATTTGGTCTAG[A/G]TATGTATACCAGCAT | 23092 |
| rs79559038 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933927 | ATTTAAAATTGCCTT[C/T]GAAAAATTCTCAGTT | 23092 |
| rs79566746 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922442 | TGTGTGTGTGTGTGT[C/G/T]TTTTCTGTAGAAAAA | 23092 |
| rs79585907 | in-del | -/AAGAA | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226505 | AAAAAAAAAAAAAAA[-/AAGAA]TGCCATGCCAGGAGA | 23092 |
| rs79603583 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787422 | GAAACCTATTTGGGG[A/C]GGTCAGGAAACTGGG | 23092 |
| rs79605230 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003097 | AGTCACGGGGTAGCG[A/G]AGGAGAAGCACCCAC | 23092 |
| rs79607308 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776192 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGGTCTCA | 23092 |
| rs79615303 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044699 | TGCTGTTAGCTTTTT[A/T]AAAAAAGTATATCTA | 23092 |
| rs79625518 | snp | C/T | 0.106278 | 0.204558 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772328 | AACATATGAACAGAC[C/T]CTTCCTTTGTCAATA | 23092 |
| rs79628159 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210275 | AAGGAGGAGTTTCCC[G/T]GCACAAGCTCTCTTC | 23092 |
| rs79628172 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174260 | CAATGGCATGCTACA[C/T]AGCCACTAAGAAAGA | 23092 |
| rs79657897 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016940 | TACAATTTAATGCAA[A/G]CCCCCCATAAGGCTC | 23092 |
| rs79658016 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957235 | TCTTTTTGATAGTGC[G/T]GTAATAAAGCCAAAC | 23092 |
| rs79659165 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944573 | GTAGGTGTATTTATA[G/T]GTGTGTGTATCAACC | 23092 |
| rs79662482 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851420 | CATTTTTGACATTAG[C/T]TAAGATAACATCAGG | 23092 |
| rs79672149 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999972 | AAGACTTGAAGAAAC[A/G]CCGGACAAAAGATGG | 23092 |
| rs79681372 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227225 | GTTTTGTGAGCAACC[A/G]TGTTCCCCAAGTAGG | 23092 |
| rs79687497 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927909 | ACATTTCCCTCATAA[C/G]TAATCAGTTTGGGCT | 23092 |
| rs79711448 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873694 | TTTTGGGATTGCCTC[A/C]CCCTCCAGCATGCAG | 23092 |
| rs79712739 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813935 | GGCCTCTGAGGGCCA[A/G]CAGGGAAGACAAGGT | 23092 |
| rs79734368 | snp | A/C | 0.101301 | 0.200969 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864089 | AGTGAGTGGGTCTGA[A/C]TTGTGTGGTCTCCTC | 23092 |
| rs79736646 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984558 | TCATCTCTCAGTGGG[A/C]TGCTATACATGATTC | 23092 |
| rs79739443 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045576 | TGAGATGGCTGGGCC[A/G]AGTGAACCTTTCATT | 23092 |
| rs79743722 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815960 | CCACCATGCTTATTG[G/T]TTTTTTTTTTTTAAT | 23092 |
| rs79745224 | snp | A/G | 0.0322114 | 0.122752 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009462 | GACCTAACTTCTCTA[A/G]TGCCTCAGTTTTCTC | 23092 |
| rs79749107 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219754 | TGTGAGCTAGTGAAA[A/G]TACAGGTTCCTGTGT | 23092 |
| rs79750693 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102467 | AGAGGCAATCTTTTT[A/C]CTCCCCTAACTCAGA | 23092 |
| rs79773516 | snp | C/T | 0.0614824 | 0.164198 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970487 | GCCATCCACTTCTGG[C/T]GGCTCCAACCTCATA | 23092 |
| rs79776789 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040100 | GATTGTGTAAAGTCC[C/T]GGGAAAGCACAAGGA | 23092 |
| rs79781437 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142959172 | ATTTTATGCTCCATT[A/G]TGTCATGCTATTATG | 23092 |
| rs79782519 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206256 | GGAGTGGCAAGTGGT[A/G]GTGTGGCTGAACTGG | 23092 |
| rs79811155 | snp | C/T | 0.0495547 | 0.149404 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806136 | TCTTGCTGTTTTGCC[C/T]AGGCTGGAATGCAAG | 23092 |
| rs79816488 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054313 | TAATAGGTAAAAAAA[A/T]TACTTGTCATTTTTG | 23092 |
| rs79828359 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790534 | TATTCCACTCTTTCT[C/T]ATCCAGAATTTCCCA | 23092 |
| rs79840374 | snp | A/G | 0.46137 | 0.133501 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985951 | ttgttattgtgaata[A/G]tgccgcaataaacat | 23092 |
| rs79840578 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193266 | TTTTTTTTTTTTTTT[G/T]AGGCAGAGTCTCGCT | 23092 |
| rs79842337 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168687 | AGCTTTTAGCAAAGG[C/T]TGTTTGGTTGCCTTG | 23092 |
| rs79860414 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143999 | CAAACATGTTTGAGG[C/T]GGGCAAGCATTCTCA | 23092 |
| rs79876844 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198862 | ACAGGTTTGTTCCAT[G/T]GGTATATTGTGTGAT | 23092 |
| rs79884721 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957575 | ACAGTAGGTTTGATA[C/T]AGATTTCTAGATCCT | 23092 |
| rs79888714 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064558 | TTCTCAAAGGACCTT[C/T]TCCAGCTATTTTTGG | 23092 |
| rs79889923 | in-del | -/GAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190035 | CAGAAGGAGGGGGGG[-/GAAA]AAAAAAAAAAGACCT | 23092 |
| rs79893397 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769232 | TAGTGCCTGCACATA[A/G]CAGACCTATTTAAAA | 23092 |
| rs79894856 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131375 | TGTAATTGGGTAAGG[A/G]TCTCATTTTCAGTAA | 23092 |
| rs79899354 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161524 | TTCCTTTGAAAGCTC[C/T]ATTTTAAAGCAGAAT | 23092 |
| rs79909520 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888781 | AAATACTCACTGGAC[G/T]CTTCTGTAAAAGTCT | 23092 |
| rs79920660 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939277 | GGAAGTCACAGTTGA[A/G]TGGTATCAACCTTTA | 23092 |
| rs79927150 | snp | C/T | 0.078151 | 0.181571 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178597 | GGTGCCACTATTCAG[C/T]GCTACTACAATAGCT | 23092 |
| rs79934145 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007038 | AGTTCGGTGAAACCC[A/C]ATCTCTACTAAAATA | 23092 |
| rs79938406 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905349 | ATGAGGACACTTTTT[A/T]GTTCCCTAACACAGT | 23092 |
| rs79964990 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876148 | GGAATGAAGTCCCCT[A/G]CTGACTTGAAGTCCC | 23092 |
| rs79967740 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818534 | TAATATCATTTAAAA[A/C]AGCAAGGTAGTGAGA | 23092 |
| rs79977846 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126314 | GGGTTGTTAGCAAGT[A/C]GTGGGTGATGATGCC | 23092 |
| rs79987803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066542 | CTGTTGGAGAAATCC[A/G]GGAACGGGAGAAAGA | 23092 |
| rs79990650 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064555 | GGATTCTCAAAGGAC[C/G]TTCTCCAGCTATTTT | 23092 |
| rs79993317 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807000 | GCCCTCAGGCTTGCT[A/G]TACTGTGCCCGTCCT | 23092 |
| rs79994957 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831783 | CTTTTTCTATCTCCC[A/G]TTATCCAGTGGGTAG | 23092 |
| rs80017270 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073490 | ATATTAAGTAATTGC[C/T]ATGGAAAAGGCACTG | 23092 |
| rs80020232 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792749 | AGCAGCGTTGGAGGA[G/T]TTGAAAAAATCCTGG | 23092 |
| rs80026949 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926956 | ACCTTCCCAGCATGC[C/T]CTGAGGTGTAATCCT | 23092 |
| rs80030092 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132875 | GTAAAAAAAAAAAAA[A/C]AAACTGTTATCTTCT | 23092 |
| rs80050933 | snp | A/G | 0.0399052 | 0.1355 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971666 | TGCCAAAAAAGTCTC[A/G]TGTATTGTTTCTTGA | 23092 |
| rs80051791 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113738 | AATGCTCTTTCTCTC[C/T]TTTGTTTTTACTTCT | 23092 |
| rs80070081 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917747 | CATGTTGCCTAGGCT[A/G]GAGTTGAACTCCTGG | 23092 |
| rs80071036 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938189 | GATTATGGGGGGGGA[A/G]GTAGGGCAAAAGAGT | 23092 |
| rs80075453 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920436 | AGATGTAAGTGACAC[A/G]TGGATATTTTCTCTC | 23092 |
| rs80078050 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081050 | CCTGGGTTTTTGGCC[C/T]TCACTGGGGGAGAAA | 23092 |
| rs80078723 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904826 | TTTGTGTTCTTTCAT[A/G]TCCTGCTCTTCATGT | 23092 |
| rs80095256 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118956 | AATAAAAAAAAAAAA[A/G]GAAAGAAGAAAGAAA | 23092 |
| rs80104351 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120586 | CCATCAAGAGGTTTT[A/G]CATTTGCCATGGAGA | 23092 |
| rs80112785 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801072 | TCCTGTTCTTGAGGC[A/G]TCTTTAACTGCATGA | 23092 |
| rs80116612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979534 | TATCTCTTGAGGGCT[A/G]GGAGTGCCACTGATG | 23092 |
| rs80142346 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929473 | AGGTAAATATGGAAA[G/T]AAAGTTATTGTTTTA | 23092 |
| rs80147845 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906877 | TTATGTTTAAACAAT[A/T]TTTTTTTTTTAACAA | 23092 |
| rs80149041 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880785 | CCTACAACACACACA[A/C]CCCTGAGTGCATCTG | 23092 |
| rs80174462 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867861 | TCCTAACTTACCTGC[C/T]TTTTTTTTCACATGT | 23092 |
| rs80184688 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142112 | TACTATGATCAAAAC[A/C]ACAGATTGACTCTAC | 23092 |
| rs80196457 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154561 | TCCCAGGCTGTCCCA[C/T]TCACCTTCCCCCACC | 23092 |
| rs80204110 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794391 | GAGGGGGGACAGAGG[C/T]CAAGGCAACGCAGTT | 23092 |
| rs80217030 | snp | C/T | 0.0410537 | 0.137264 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069542 | ACATCTGTACTAAGG[C/T]GGTAGTTGGGGACTC | 23092 |
| rs80221093 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129295 | CTTCTTGTGTGTCTC[C/T]TTTTTTATTGACTAC | 23092 |
| rs80234440 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807423 | TTTCTACACCAGATT[A/G]TATTCCCAGAGGCCC | 23092 |
| rs80237760 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999700 | CATAGGACAAAATCT[A/G]TGCGATCTGGGATTG | 23092 |
| rs80237872 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969278 | CGTTTAGTTTGTTTC[C/T]TCTTCTCCACTAGTA | 23092 |
| rs80239622 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129971 | AACCCTACTCTGTCT[A/G]GCTCCAAAGCCTGTT | 23092 |
| rs80246029 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024219 | TTGTTTGATGAGACC[A/C]TGGCCCCCAAAGCTA | 23092 |
| rs80268184 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952414 | GAGTCAGAGGTACTC[C/T]CATCTGTTTTGGTGT | 23092 |
| rs80278365 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087293 | TGCCACTTGTGCTAT[A/G]AGAACTTGGTTCTTT | 23092 |
| rs80285904 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819283 | AGCAGATTGGCCCCA[A/G]TAGGTCAGAGGTCAA | 23092 |
| rs80288163 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038711 | TTTTTTTTTTTTTTT[G/T]TTTGAGACAGAGTCT | 23092 |
| rs80297819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188830 | GAAAGTGAGGGTAAC[C/T]TAGAAAAAGGAGGTG | 23092 |
| rs80300479 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921152 | TCCCAACCTAGCATT[C/T]CACATCCACTGTCAA | 23092 |
| rs80306750 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075100 | AGCTGCATGTTTTCT[G/T]TGCTGGTTACTTTTT | 23092 |
| rs80317864 | snp | A/C | 0.130008 | 0.219321 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892375 | CAGGACAGAAATCCC[A/C]GCTCTGCCGTATACT | 23092 |
| rs80320505 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146723 | TTAGACTGGTGGAGT[C/T]GTAAGGACATTGGTG | 23092 |
| rs111254964 | snp | A/G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211520 | GTCAGTTGCCTATCA[A/G/T]CTTGAGAAAAAAACA | 23092 |
| rs111255704 | snp | C/T | 0.5 | 0 | intron-variant, synonymous-codon, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207462 | AGAAGAAGCGGTACA[C/T]GAAGACTCCAGGTAA | 23092 |
| rs111257134 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940770 | TGAACATATGCATGT[A/G]TATGTCTTTATGGTT | 23092 |
| rs111259878 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953132 | GCTTGACAAAATGAA[C/T]GCCCACACCAACCAG | 23092 |
| rs111297065 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857175 | ATTTAGGACCCGTCC[C/T]AGTCCTATATGACCT | 23092 |
| rs111303163 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903918 | TTGCTCTTCTCTCTC[A/T]AATGTTACTCTACTC | 23092 |
| rs111305684 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907247 | GATGTCTGTGCACAG[A/T]GTCACAGAGCAGCTG | 23092 |
| rs111308376 | snp | G/T | 0.0494327 | 0.149241 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844397 | TTTCCATGAATGAGT[G/T]AGCAGTTTTAAAGCT | 23092 |
| rs111324855 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948881 | AGGCCTAGGCGGATG[G/T]ATCACCTGAGGTCAG | 23092 |
| rs111379266 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833039 | CACTCATAATCTTAC[C/T]ACAGAGAACTTTTAT | 23092 |
| rs111390231 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047951 | TCCCAGGTTCCAGTG[A/G]TTCTCATGCTTCAGC | 23092 |
| rs111406086 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128687 | CATGAGAAGGAGTGA[C/G]CTGTGCTCAACTGTT | 23092 |
| rs111409332 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958219 | TTTAAACAAGTTTTA[A/G]GATTATGTTAACTCA | 23092 |
| rs111414988 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879156 | TTAAATAATCAGTAT[C/T]AATCATGCATGGGAG | 23092 |
| rs111425658 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205637 | TGTCAGAGGGAGTAC[A/G]CTGGCTGCAGGAGCC | 23092 |
| rs111428683 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992679 | TGATCCGCCTGCCTC[A/G]CCTCCCAAAGTGCTA | 23092 |
| rs111459103 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815960 | CCACCATGCTTATTG[-/T]TTTTTTTTTTTTAAT | 23092 |
| rs111477549 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838369 | TCCTCCTTATAGCCA[A/G]GCTTTCATTGTTCTT | 23092 |
| rs111480881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115171 | AACCCCGTCTCTGCT[A/G]AAAATACAAAAGTTA | 23092 |
| rs111483788 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114280 | GGGCAGTCCTGCAAG[A/C]TGTGTTCATGGCCCT | 23092 |
| rs111504019 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149097 | TTTTTTAGGTGTCTA[A/G]ATACGATTTATTTTC | 23092 |
| rs111505843 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178457 | GAAAGATGGGAGACT[A/G]CAGTTCCTTCCACAT | 23092 |
| rs111510621 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879578 | CAGAAAATCTTAGGC[A/C]GAAAACTCTATAGAG | 23092 |
| rs111530938 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198297 | CAATTGTTACCATAT[A/G]AACACTTTATAATGC | 23092 |
| rs111531002 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097347 | ACAGAGAGAGACTCC[A/G]TCTCAAAAAAAAGAA | 23092 |
| rs111541718 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850406 | GGTGCTTACTGCTTT[C/T]TCTTTTTCTTGCAAC | 23092 |
| rs111556779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184637 | CTCCTGTCTCTCATC[A/G]GCCCCCTTGTTCTGA | 23092 |
| rs111560206 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781143 | AAGGGCCTCTGGGGG[A/G]GGGAGCAGAGGCCTG | 23092 |
| rs111567775 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964191 | CCTGAAGGATATAAC[-/A]GTTATGTTGAGGAGA | 23092 |
| rs111579376 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147706 | TTACAAACGTCCAGG[G/T]ACTGTAGCAGCTCTG | 23092 |
| rs111584282 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821449 | TCTTACATTTTTCTA[G/T]GTGGTAGAGTCCTTG | 23092 |
| rs111586444 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139806 | ACACAGATACACCAT[C/T]CAGCAGAGACTGTAC | 23092 |
| rs111588214 | in-del | -/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824408 | CAGAGCTGGAAGTGT[-/G]TGGTCCCCAAGGCTC | 23092 |
| rs111596425 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121219 | GAATTGACCTTCAGA[A/G]TTGGCTCAGATTTGC | 23092 |
| rs111614576 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799456 | CATCTTTCAACAGTC[C/T]CAAGAGTGGATGCTT | 23092 |
| rs111618546 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884972 | GCCCCCAACCCCTGG[C/T]TGCCTTCTGGCCTTG | 23092 |
| rs111651378 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093742 | CTGTTCTCCCCTCTC[C/T]TTCCCCTTCCCCTAG | 23092 |
| rs111652919 | snp | C/G/T | 1.64787e-05 | 0.00287038 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913187 | TCTTGATAGTCTGTG[C/G/T]GTTCCCACTAGGGAG | 23092 |
| rs111657247 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864103 | ACTTGTGTGGTCTCC[C/T]CTTAATTCACCACCC | 23092 |
| rs111661719 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123984 | ACACACACACACACA[A/C]ACACACAATGTCTAG | 23092 |
| rs111662577 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038718 | TTTTTTTTTTTTGAG[A/T]CAGAGTCTCTTTCTG | 23092 |
| rs111673462 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109891 | CTCACTCAGTCAAGA[A/T]CAAAGCTTTTACAGT | 23092 |
| rs111676637 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790580 | ATTCGTCATACAGTT[-/C]GGACACCTTACCATG | 23092 |
| rs111681821 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199755 | ACTGCCTGGCAGAGA[C/T]GTGCAAATGCCAATT | 23092 |
| rs111691642 | snp | A/G | 0.5 | 0 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229313 | ATTCTTCCTAAATTT[A/G]ACTTTCTAATCACCT | 23092 |
| rs111692969 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215846 | ATAGCACATTTTATG[C/T]AAGCTTATTCATCAG | 23092 |
| rs111694351 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956897 | CTCATGAGACTTACT[A/G]TCATAAGAATAAGAT | 23092 |
| rs111707470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796687 | CCTGTGGACTCTGGC[C/G]CCTGCCAGCTCCTCC | 23092 |
| rs111707959 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991815 | TCTATGATGTTTGTA[C/G]GGCAACAAAATTGCC | 23092 |
| rs111720559 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220895 | TTCTTGCGTCTTTCC[C/T]TACAAACTGAAACTA | 23092 |
| rs111724163 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091421 | TAATTTCTAAGAAAC[C/T]GATCTTTTGTTTTAA | 23092 |
| rs111752655 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835300 | CTTAACCCATCAGAG[A/G]TAGAATTTATGGTAT | 23092 |
| rs111770258 | in-del | -/ACTGGCT | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178573 | CTGCCCTGCCCCTTG[-/ACTGGCT]TAGGTGCCACTATTC | 23092 |
| rs111784689 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045827 | ACATGGTGAAACCCC[A/T]TCTCTACTGAAAATA | 23092 |
| rs111802038 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855947 | AAATGAGTGGTCTTT[A/G]TGGCATAGTCTACTC | 23092 |
| rs111809738 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976588 | TCAATGAATAAAAGC[A/G]CACCTAAGTAAGACT | 23092 |
| rs111810969 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155030 | TTTGTGGAGAAGGAT[C/G]TTTCCTTTTAGATGG | 23092 |
| rs111838033 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922445 | GTGTGTGTGTGTGTT[C/T]TCTGTAGAAAAAAAT | 23092 |
| rs111848133 | snp | C/T | 0.00319074 | 0.0398324 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092843 | TGCAAACAGCTCCCA[C/T]GTCTGAGCAGACCAA | 23092 |
| rs111859783 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953645 | TGGGACTTGCCAAAA[A/T]TAAGGCAGCCTGTCC | 23092 |
| rs111914637 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790482 | GAATCCATTTCTTAC[A/G]TGGCAGGCAGACCAA | 23092 |
| rs111924046 | snp | A/T | 0.0287284 | 0.116357 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227567 | CACAGCCCCACAGCA[A/T]GCCTGAGACAAGACT | 23092 |
| rs111932482 | in-del | -/A | 0.381113 | 0.21286 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984922 | TTATTAAAAAAAAAA[-/A]GCGGTCAGACAGCCT | 23092 |
| rs111970483 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129856 | CAGTAGCTCTGCAAG[A/G]CAGGTATTAGATCCT | 23092 |
| rs111990321 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070667 | ATAATCCCAGCACTT[C/T]GGGAGGCCGAGATGG | 23092 |
| rs111990933 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839106 | TGCATTTTAACAAAC[A/G]TTTCAGACGATTCTT | 23092 |
| rs111995762 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890339 | AACACCAGGTGAAAA[G/T]GTTGTGGGAAAGAAA | 23092 |
| rs112001557 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120665 | AATTAAGAGGGATTA[A/G]CAGTTACCTGGACTT | 23092 |
| rs112003239 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103225 | AAAAGTCACTGGATC[A/G]GTAGACATGGGAAAA | 23092 |
| rs112036538 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901870 | TGTTGGGAGCTCAGA[C/T]ACAGCTACATAATAC | 23092 |
| rs112054489 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123479 | ATAAACTCCCTGCCA[A/G]TAGAACTTAACTTTA | 23092 |
| rs112062581 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811457 | ACGCCGACAGCATGG[C/G]TTCCAATCCTGGCCT | 23092 |
| rs112085259 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907466 | CACTGGATGTAGCAT[C/T]AATGGGAAACAGTCT | 23092 |
| rs112088559 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084523 | GATTTGGAGGGAGGC[A/G]TGTTTTTAACCAAAA | 23092 |
| rs112097461 | in-del | -/AG | 0.13446 | 0.221699 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813464 | AGGGAACTGGGTGAC[-/AG]GGGTGACTTGGACAG | 23092 |
| rs112107489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209987 | ACTTCCAGAGCATGA[A/C]GCTTCAGATTTCCTT | 23092 |
| rs112110519 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081142 | AAAAGTTCTACTGAG[A/G]GCTCTCAGCATACAG | 23092 |
| rs112111674 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129387 | CCTGGGACTTTTTAC[A/G]GATAAGGTCTCTGAA | 23092 |
| rs112126213 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209780 | GCTAGACTCCATCTC[-/A]CAAAAAAAAAAAAAA | 23092 |
| rs112151160 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774333 | CTTAGTTGGACTGAA[A/G]AAATTTGCATCCAGT | 23092 |
| rs112157947 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073558 | CGGTAGGGGAGAGCA[C/T]TGGCCCAGCAGGCAA | 23092 |
| rs112160289 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074597 | TTTTATTGGAACAGA[A/G]CCATGCTCATTTATT | 23092 |
| rs112162505 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107550 | ATGACAGCAACTAAG[A/G]TGTCAGGCTGTGATG | 23092 |
| rs112163591 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016450 | TGGCTCACGCCTGTA[A/G]TCCCAGCACTTTGGG | 23092 |
| rs112166201 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845128 | TGAGGGAGGCTGCTA[C/T]GAGAGCAGGGAAAAT | 23092 |
| rs112178817 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829573 | GGAGAGGGTGAGGTG[C/T]AGTGTGATATAATTG | 23092 |
| rs112182498 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903417 | AAGGGAGTATTTGGC[C/G]AGTTCCTGGAAGGTT | 23092 |
| rs112185790 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935964 | GGTGTTTGCTGTCAC[C/G]ACTCTTACTCAGCAG | 23092 |
| rs112188905 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827232 | TGTTGGCTGGCCTCC[A/T]TGGTTGGTTGTGGCA | 23092 |
| rs112208446 | snp | G/T | 0.0441095 | 0.141807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871002 | TCCTCTATCAAGCCT[G/T]AGGTGAGTTCCTTTT | 23092 |
| rs112210647 | snp | A/G | 0.067446 | 0.170804 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177315 | ACATAGTGCTTGTCA[A/G]ATGAAGGAATCAGCT | 23092 |
| rs112217181 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973185 | GTGTTTGTTGCAGCA[C/T]TGGTGGAAAAGCTAA | 23092 |
| rs112235151 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991671 | ATACAGAAATACTAT[C/T]GTGTGTCAGTTGCCT | 23092 |
| rs112254353 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106712 | TCCTGACCTCAGGTG[A/T]TCCACCCACCTCGGC | 23092 |
| rs112258555 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134906 | GCAAGGGCCAATTAC[C/T]GAGAGCAGCTACTAC | 23092 |
| rs112273760 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121742 | TTTCCTCATCCCCCA[A/G]TTTGAAGAATATTAA | 23092 |
| rs112293866 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843306 | CACTCCTGGGAGCCA[A/G]ATTGAGGCCTGTGTC | 23092 |
| rs112298497 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819207 | AACATTCCTCAGTTT[C/G]CTTGTCTAACGTCAA | 23092 |
| rs112316174 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010361 | TCTCAGGTTCCATAT[C/T]TCTAAAATGTGAATA | 23092 |
| rs112335246 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938278 | TTAGCTATTCAGATA[G/T]TCAGATAAAGCTTTG | 23092 |
| rs112339104 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083125 | GGAGACTTTTTCTTC[A/G]TCTTCTTCCTTTTTC | 23092 |
| rs112353380 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101963 | AGGGGCTGTGGTGGC[A/G]CTGATAGAACTGGAG | 23092 |
| rs112359629 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833901 | TATCTTGACCTTGGC[A/G]TTGGTAAATTTTCTG | 23092 |
| rs112363966 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157707 | TGGATGGCATTACTA[C/T]GGTAGAGATCCTTTC | 23092 |
| rs112405784 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824353 | TAGTTCCTGAGGGTC[A/G]TCCCTATCAAACACC | 23092 |
| rs112414594 | in-del | -/AG | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173989 | GGGCAGCATCAAAAC[-/AG]AGAAGTGTTGTATCT | 23092 |
| rs112436250 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189367 | ACTTTGTTGAGATCT[C/T]GGCTCAGATGTCACC | 23092 |
| rs112450008 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109908 | AAAGCTTTTACAGTG[A/G]CCTGCAAAGTTTTCC | 23092 |
| rs112451345 | snp | C/T | 0.155656 | 0.231515 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847337 | GCTTAGGTCACACAG[C/T]GAATACAGCAAAGGA | 23092 |
| rs112461961 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143808 | CATGTCCCTGCCCTC[A/G]GGTAGTTTGCATCCT | 23092 |
| rs112466523 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176556 | ACATAGAAGTCCTTT[C/T]ACCACTGAATGTAAA | 23092 |
| rs112468664 | in-del | -/TGTG | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796055 | ACTAAGGTGTTTTTC[-/TGTG]TGTGTGTGTGTGTGT | 23092 |
| rs112471095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202608 | AACCAAAAAAGAGCC[C/T]GTATAGCCAAGACAA | 23092 |
| rs112485559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221792 | CCTCCCAAGGTACTG[A/G]CATTACAGGCGTGAA | 23092 |
| rs112485632 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882788 | GGGTGTTCTTATTTT[-/T]ATTTTGTTATATGGT | 23092 |
| rs112491217 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818388 | GCTGTGCCCATAGGT[A/G]TGGCATTGCTGGCTG | 23092 |
| rs112492540 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796984 | GTCAGAAACTGACTA[A/G]CCTGGTTGGCTATAT | 23092 |
| rs112497280 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221059 | ACATTAAGAGTAAAT[A/G]TCCTGCCTCACTGCA | 23092 |
| rs112513206 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037786 | TTAGTGAAGATAAAG[A/G]TGTAATTGTTTTCCT | 23092 |
| rs112528197 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948833 | AAACAGGTCGGGTAC[A/G]GTGACTCATGCCTAT | 23092 |
| rs112528269 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903854 | ACCTTTGTTTTTCTT[C/T]ATGAATGGGAATTCC | 23092 |
| rs112540925 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799796 | ACTCACTCCCATGAT[C/T]ACAGCATTGATTCAT | 23092 |
| rs112575041 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206397 | AAATCCACAAGCCAC[A/G]TTTCAGTGAGTAATT | 23092 |
| rs112618936 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066266 | GTGTGCAGCAGGCTC[A/G]ACCATCTATCTGGGT | 23092 |
| rs112623056 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795094 | ATAATGTAAAAACCA[C/T]TCCTAACTCACAGGT | 23092 |
| rs112625612 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889542 | AGAATCACTTGAACC[C/T]AGGAGGCGGAGTTTG | 23092 |
| rs112630382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128564 | AATTTGGCTTCTTAA[C/T]AGTTACAATACATAA | 23092 |
| rs112638740 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835468 | AAGAAGAGTCTCTGA[C/T]TCATCAAAAACATCC | 23092 |
| rs112646868 | in-del | -/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181767 | TTGAGATGTTAAGGA[-/C]TTTTTGTTTTGTTTT | 23092 |
| rs112664710 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851389 | GGCGTGAGCCGCTGC[A/G]CCCAGCCGGAAAATA | 23092 |
| rs112680659 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024065 | GCTGTGGTGCATTGA[A/G]CTTGAATTACATTTA | 23092 |
| rs112713873 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785023 | GCTCCGCCTCCCTCC[A/T]GAGTTCATGCCATTC | 23092 |
| rs112719121 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102611 | CCCCTGTGCCTGTTG[C/T]GTCGCCCATCCGGGC | 23092 |
| rs112732210 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139897 | AGGGGGAGCCAGAAG[A/G]ATTGAAGGGAGCCAG | 23092 |
| rs112739189 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986895 | CAGTACCATGCTGTT[C/T]GGTTACTGTAGCTTT | 23092 |
| rs112751519 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902466 | CTCAAAGGATGTTCT[C/G]TTGTCCAACTCTTAG | 23092 |
| rs112756665 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999468 | AGAGGAGAGTGAGGC[A/G]GGTTAAGGCTACTTT | 23092 |
| rs112767667 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026227 | TGGATTGTATTTATT[A/C]TTTCAGGACATATTT | 23092 |
| rs112768583 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071877 | TCCACTGCACTCCAG[C/T]CTGGGCAACAGAACG | 23092 |
| rs112770897 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010903 | AAATGCAGGGATCAA[A/G]GATGGCTGAAGAAAA | 23092 |
| rs112770960 | in-del | -/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038259 | ATACACTTTTTTTTC[-/C]ATAAGGACTGTGAGG | 23092 |
| rs112789133 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095234 | TGAAATTCACTTAAC[A/G]TAAATTAGCCATTTT | 23092 |
| rs112802614 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867225 | GGCCACAGGTAAGAC[C/T]GTGTGTCACGGAAAC | 23092 |
| rs112803309 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071678 | TTTGGGAGGCTGAGG[C/T]GGGCAGATTGCCTGA | 23092 |
| rs112812729 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822880 | CCTGGTGCCAGGCAC[A/G]TGGGAGACCAGTCAG | 23092 |
| rs112824459 | in-del | -/AAAC | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820450 | CTTAAAAAAACAAAA[-/AAAC]AAACAAACAAAAAAA | 23092 |
| rs112824497 | snp | G/T | 0.0766824 | 0.180169 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983268 | CTGGAGTACAGTGGC[G/T]CAATCTCTGCTCATT | 23092 |
| rs112845750 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213100 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 23092 |
| rs112863100 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225886 | AGCTACAAAACTGGA[C/T]AAACTTCAGAATATG | 23092 |
| rs112891877 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882514 | CTCATGAAGTAGCTG[A/G]GGTGAAAGACATCAG | 23092 |
| rs112894785 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088614 | ATAAAGTTTCGGTGC[C/T]GCAAAAGGAATAGCA | 23092 |
| rs112902627 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837006 | ACCCCATTGATGTGT[A/C]CTTCAGGCACCCTTT | 23092 |
| rs112905698 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007194 | CAAGACTCTGTCTCC[A/G]AAAAAAAAAAAAAAA | 23092 |
| rs112912765 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149886 | CTCCTTTATTTCACT[A/G]TTTTTCATAATGACT | 23092 |
| rs112915201 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935100 | TTATTTTAATTCAAA[A/T]GTGGGAAACTCAATT | 23092 |
| rs112915260 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793668 | TCTCGGCTCACTGCA[A/G]CCTCCACCTCCCGAG | 23092 |
| rs112918861 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097813 | GGTGACAGAACGAGA[C/T]TCCAACTCAAAAAAA | 23092 |
| rs112919594 | snp | C/T | 0.00019999 | 0.00999775 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143121141 | CCTAATAGAAAACCA[C/T]GAAAAGGTAATATGT | 23092 |
| rs112919812 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794401 | AGAGGCCAAGGCAAC[A/G]CAGTTACTCCACACT | 23092 |
| rs112951021 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182247 | GGAACACAAAGCACT[C/T]GGCTTTGGTGCTAAC | 23092 |
| rs112951894 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834702 | CAAAGGTGGAAGCTC[C/T]GGGCCTCTTGAGGCC | 23092 |
| rs112967551 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906846 | TTGATAATTATTAAA[C/T]GTCTGCTAATTCTCT | 23092 |
| rs112975979 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115106 | GGGAGGCTGAGGCAG[A/G]TGGATCACCTGAGGT | 23092 |
| rs112988858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937324 | TATCATTAGCCATTA[A/G]GGAAATGCAATCTAA | 23092 |
| rs112989790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140789 | GGGCCTTGTTTTACA[C/T]GGATCATGTTAACTA | 23092 |
| rs113015203 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841776 | GAAGAGGGTAGAGAC[A/T]AGGAAAGTAGAGTAG | 23092 |
| rs113023822 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221951 | GGAAGGAAGGAAGGA[A/T]GGAAGGATGGATACA | 23092 |
| rs113027541 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142714 | ATTCCAAGCTTCCCA[C/T]GTACTTGGGTATTTC | 23092 |
| rs113036086 | in-del | -/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036633 | AGTTTGATGGTATGG[-/G]CTCTAGAGCAAGTCT | 23092 |
| rs113037196 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809010 | ATAAGATAAGTGCCT[A/G]TATGGCTGGCTGTTC | 23092 |
| rs113053407 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956748 | AAGAAAGAGGTTTAA[C/T]TGGATTTACAGTTCC | 23092 |
| rs113055432 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215395 | AACTATCAAAAGTTA[C/T]GTATATGCTTCTGTC | 23092 |
| rs113065735 | snp | C/T | 0.151001 | 0.229563 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163601 | GATTACAGGGGTGCA[C/T]CACCACACCCAGCTA | 23092 |
| rs113071834 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912190 | CTATGAGATGAAATT[A/G]TCACATTCAGTTGAA | 23092 |
| rs113079404 | snp | A/C/G | 4.94934e-05 | 0.0049744 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014125 | GAAGGGAGTAAGTAC[A/C/G]ATGCTTGGGTAACCT | 23092 |
| rs113080032 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123275 | ATTCATAGGGTTTGT[C/T]GTCTTTGTGAGAGCA | 23092 |
| rs113089872 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853322 | CTGCCTCCCAAGTAG[C/T]GGGGACTGCAGGCAT | 23092 |
| rs113097930 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204937 | CCTGGTTCTGCTTGG[G/T]TTCCTGGGCTGGGCT | 23092 |
| rs113100143 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869224 | TTTTTTTTTTTTTTT[G/T]GAGACAGCGTCTCAC | 23092 |
| rs113101142 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196092 | GTGTATTAAAAAGTA[C/T]ATGAAATATAAATGT | 23092 |
| rs113104484 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851151 | TGCCCAGGCTGGAGT[A/G]CAGTGCATGATCTCG | 23092 |
| rs113118027 | in-del | -/TCT | 0.334871 | 0.235153 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795038 | AGTGTCTCTGTCATA[-/TCT]TCTTCTTCTTTTTTT | 23092 |
| rs113118179 | in-del | -/GT | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844107 | CCAGGCTAGAGTGTA[-/GT]GTGGCACGATCTCGG | 23092 |
| rs113118273 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220321 | TGGTTTTACTAGGTC[A/G]CTACTAGGAGGGGGT | 23092 |
| rs113122550 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119563 | ATTCTGGGTAGAATG[A/G]AAAACATAAGTAAAA | 23092 |
| rs113122616 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970085 | TACTGTTAGTCATGT[G/T]AAGCAGATGAACAGG | 23092 |
| rs113145359 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200252 | CAGCAGTAGAACCTT[G/T]CTGGAAAGCTATTTG | 23092 |
| rs113148194 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069634 | AAGGAAAAATTGGAT[A/G]CCATCATTCAAAAGA | 23092 |
| rs113149440 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996453 | AGCCAAGATCACGCC[A/G]CTGCACTCCAACCTG | 23092 |
| rs113161367 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090258 | ATGCAGCCCATGCCC[A/G]GTTGACTGGAGGACC | 23092 |
| rs113162184 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876780 | AGACCCTGTGTCAAA[A/C]AAAAAAAAAAAAAAA | 23092 |
| rs113189153 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092277 | CACGCCATTCTCCTG[C/T]CTCGGCCTCCTGAGC | 23092 |
| rs113191756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202666 | GAACATGCTACCTGG[A/G]TTCAAACTATATTAC | 23092 |
| rs113192312 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042403 | TTCTAGATTTCAACC[A/G]AATACCTGTCACTTG | 23092 |
| rs113198198 | snp | C/T | 0.0581099 | 0.160244 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225193 | TTTTTATTTGTGTTT[C/T]TGTTTGTTTTTTGAG | 23092 |
| rs113199273 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097623 | CAAGAGATTGAGACC[A/G]CCCTGGCTAACACGG | 23092 |
| rs113203689 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094297 | TCTGTGCACAGAGTC[A/G]TTGCCACAGTATGTG | 23092 |
| rs113207295 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774474 | AGTGGGAAGTGTAGA[A/G]AGTTCCCACATAGCG | 23092 |
| rs113220285 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854935 | GTGCTGTTCAAAGGA[A/C]CCCCCAGTCCCTTTT | 23092 |
| rs113221731 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997594 | TTTTTTTTTTTTTTT[A/T]TTTAGTAGAGACAAG | 23092 |
| rs113239042 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120511 | TGGTTTTAAATATCC[A/G]GATCTGCCCATTTAA | 23092 |
| rs113241445 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100386 | TGTGTGGGAAATAGC[A/G]AAGGAACATCCAGTC | 23092 |
| rs113251776 | snp | C/T | 0.320335 | 0.239902 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097678 | ACAAAAAAAATTAGC[C/T]GGATGTGGTGGCAGG | 23092 |
| rs113265006 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193245 | ATTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs113275343 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157719 | CTATGGTAGAGATCC[C/T]TTCAGAGAACAGAGA | 23092 |
| rs113308385 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904525 | CCCTGTCTCTTAAAA[A/G]AAAAAAAAAAAAGAG | 23092 |
| rs113309292 | snp | A/C/T | 0.0766824 | 0.180169 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991491 | GCCCCACTGAGATGA[A/C/T]CCCACTACCTCAGCT | 23092 |
| rs113321021 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083742 | GAACTCAGGTGATCC[A/G]TCCACCTCTGCCTCC | 23092 |
| rs113325656 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880623 | TCAATGAAAGCAAAA[A/G]GATTTCCAACGTTTT | 23092 |
| rs113328024 | snp | A/G | 0.095934 | 0.196885 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202522 | TAATTGATAGATTCA[A/G]TGCTATCCCCATCAA | 23092 |
| rs113328439 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066952 | GTGATTCAAATGCTC[A/T]GTGGGGTGGTGCACC | 23092 |
| rs113330253 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835748 | ATTAGGTAACCCATG[A/G]TTAGCACATGATACA | 23092 |
| rs113335980 | in-del | -/T | 0.120674 | 0.21395 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190557 | AAAGTGAAATAAAGA[-/T]ATTCCCAGACAATTT | 23092 |
| rs113337848 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104489 | GCACTCCAGTCTGGG[C/T]GAGAGAGTGAGAACC | 23092 |
| rs113348018 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118802 | TGTGGGGTGGGGAGA[A/G]GGGGGAGGGATAGCA | 23092 |
| rs113354249 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785544 | AGCGTGTTATTTCTG[C/T]TTGAGAATGGGTACC | 23092 |
| rs113355545 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081569 | GGGACCTCCAGAAAA[C/T]TACCTACCATCCGAA | 23092 |
| rs113357672 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896482 | AATAGATGTTTACTT[C/T]TCACACATCTGTGAG | 23092 |
| rs113366325 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176803 | GAAAATTTCCACCAT[A/G]AAAGAGACTCGGGTG | 23092 |
| rs113369455 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196616 | ACACACATTTTCTCT[A/G]TAAGGCACATTACAA | 23092 |
| rs113371099 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208734 | GTGCAGCTCCCAGCC[A/C]AGAGCCTGACTTGCT | 23092 |
| rs113380754 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822998 | TGATGTTGATAATAG[A/C]AGCTATCATTTATTG | 23092 |
| rs113385105 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800966 | TCCTGTTCCTCCCTG[A/T]TGGGGAACATCAGGT | 23092 |
| rs113396242 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153332 | GACCTGAGCATGCCC[A/G]CTACCACCATCTTCC | 23092 |
| rs113401251 | snp | G/T | 0.123452 | 0.215605 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985249 | TTAAGCTAAATGTTA[G/T]TACAAGAATCAAAAA | 23092 |
| rs113406277 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942533 | CTGTGGTGTGTTGCC[C/T]GCATTCATATTTGAA | 23092 |
| rs113413294 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858112 | GAGAGAGAGAGAGAG[A/G]GAGTGTGTGTGTGTG | 23092 |
| rs113446846 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099683 | AGTGAAGTTCCTCTG[C/T]TGATAAGTCCAAAAT | 23092 |
| rs113452371 | snp | A/C/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143232 | GAGCCAGACCTGTTC[A/C/G]GGCCTGCCAAGACGT | 23092 |
| rs113453963 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044193 | GAATAGTTTACAAGG[-/A]AAAAAAAAGCATCTA | 23092 |
| rs113488506 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791727 | CCAGCACTTTGGGAG[A/G]CCAAGGCGGGTGGAT | 23092 |
| rs113510930 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092549 | CATAAATTCTCCCCC[C/T]CCCACCTTTTTTTTT | 23092 |
| rs113530584 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873161 | GCCTTTAGAAAGTAG[A/G]GATAGAACTTAAATT | 23092 |
| rs113537864 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814257 | AACACCATGGCTAGA[A/G]CCTTCCGGTAATCTG | 23092 |
| rs113545108 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158161 | CCCTAGTGTTGATTT[C/T]TTTCCGTGGTGGCAG | 23092 |
| rs113557943 | in-del | -/TAACTCACACC | 0.474723 | 0.109542 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109154 | TAGCTGGGTAGCAGG[-/TAACTCACACC]TAACTCGCACCTAGA | 23092 |
| rs113558059 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770614 | TTGCGCGCCGGCGGA[C/T]ACCGCGCGCGGAGTG | 23092 |
| rs113567052 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784176 | CAAGATGGGTTTCTC[G/T]CTGGAAAGAAAGCCT | 23092 |
| rs113571413 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185010 | GTGGATTTTTACCCC[C/T]GTATTATTTACTATA | 23092 |
| rs113573068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138945 | ACACTGTTAACCAGT[C/T]GTTATTTTGCTTTCA | 23092 |
| rs113575873 | snp | G/T | 0.0829062 | 0.185956 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176053 | CAGGAGGTGGAGGTT[G/T]CAGTGAGCTGAGATG | 23092 |
| rs113579833 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904596 | GAATGCCAGGTGCTG[C/T]TAACATGGACATTTT | 23092 |
| rs113581802 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207568 | CTGTGGTTCCATCCT[A/G]AGAGACCAGAGCTAA | 23092 |
| rs113583642 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085994 | TTAATAATTTTTTTC[A/G]CAAAGAAACAAGGCA | 23092 |
| rs113584136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036722 | TTCATCTGTAATATG[A/G]GCTAGTGATAATGTC | 23092 |
| rs113594227 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880677 | AGTCAATTCAGCTGC[G/T]GTCTCTTACGCCACC | 23092 |
| rs113596864 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903979 | ATGTACCATACCCTG[A/G]GCATAGCAGCCTTGG | 23092 |
| rs113597612 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912354 | TAAAATTATAGACTA[C/T]GCAAACTAATCAATA | 23092 |
| rs113603692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149858 | CAGGAAGCTATCTGT[C/T]CTTTTTATTTCACTC | 23092 |
| rs113610515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215237 | TTGAGAGATTCCTAC[A/G]TTGACAGGTGAATCC | 23092 |
| rs113632964 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142879396 | ATGCCAGCGAGGTGC[C/T]CATCACTCCCTTGGA | 23092 |
| rs113636186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911122 | AGACCCTGTGTGTGA[C/T]GGAAGAATTTCCCTG | 23092 |
| rs113665226 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141183 | CTGAAAACCACGTTG[A/G]TAATGTGGCTATTAA | 23092 |
| rs113667931 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893397 | CTGTGCCTTCACTTG[A/T]CATAATGACCTCCAG | 23092 |
| rs113668758 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195901 | GCACAAAAACTTTGC[A/G]TATGGGAACAAGGGA | 23092 |
| rs113670211 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788030 | ATGGAGTCTTACTCT[A/G]TTGCCCAGGCTGGAG | 23092 |
| rs113709160 | snp | A/G/T | 0.0811548 | 0.184367 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205492 | TATCACTGTATTGTC[A/G/T]TTTTCCCTTGCAAAT | 23092 |
| rs113719524 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120416 | ATTTCTGTTTATGCC[A/C]TGTTTCACTTAATGT | 23092 |
| rs113720028 | snp | A/G | 0.039522 | 0.134904 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128742 | AAACAAACCAATCCC[A/G]CATTACTAGGGACCC | 23092 |
| rs113725731 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045795 | CTGAGGTCAGGAGGT[C/T]GAGAGCAGCCAGGCC | 23092 |
| rs113728752 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199986 | TCTCTTTATCCATCA[G/T]CCTGTCTCCTTCCCC | 23092 |
| rs113734228 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788254 | GATCCACCCACCTTG[C/G]CCTCCCAAAGTGCTG | 23092 |
| rs113737695 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014923 | CCTACTGTGAATTCC[A/G]GTTGTGTTAGGAAAA | 23092 |
| rs113757832 | in-del | -/GTG | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080919 | TGGACTAGGGTAGTA[-/GTG]GTGGAAATGCTGAAC | 23092 |
| rs113766287 | snp | A/T | 0.0759472 | 0.179459 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985952 | TGTTATTGTGAATAG[A/T]GCCGCAATAAACATA | 23092 |
| rs113771839 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823884 | TCTCATAAGGCCTGT[C/T]GTGACAGAATTTTCA | 23092 |
| rs113776868 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073188 | CAACTGAATTCCTAA[C/T]AAACTAATCCATAAA | 23092 |
| rs113801037 | snp | C/T | 0.0768335 | 0.180315 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120947 | GTATCTCTGTGTACA[C/T]GATTTGTCTCATTGG | 23092 |
| rs113812591 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130786 | AGTTAAATAAACAAC[A/G]GTCACTTGGGGAATG | 23092 |
| rs113815637 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851257 | GTGTGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 23092 |
| rs113816080 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900570 | GCTATATACTTTTGT[G/T]CTTACTATTCCTGCT | 23092 |
| rs113820719 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203450 | AGGATGTGGAGAAAC[A/G]GGAATGCTTTTACAC | 23092 |
| rs113829940 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019530 | GACTATGAGAATTGG[C/T]TCATTTTTCTTTGTA | 23092 |
| rs113837276 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811491 | CGTCACGTGTAGTTG[A/G]TAAGTACCTTATCTT | 23092 |
| rs113842165 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895493 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 23092 |
| rs113843694 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147627 | TACTGTCCTGCTGAG[A/G]TGGCTTTGGTGATAG | 23092 |
| rs113845723 | in-del | -/AAAC/ACAC | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123964 | TTTTCTGTAATAGAA[-/AAAC/ACAC]ACACACACACACACA | 23092 |
| rs113852297 | snp | A/G | 0.0119091 | 0.0762411 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222564 | ACTGACTCTGTTGCT[A/G]CCTGTCAACATGAAT | 23092 |
| rs113884211 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994974 | AAACTGGCTAGCCAT[A/C]TGGAGAAAACTGAAA | 23092 |
| rs113885013 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869184 | AATCACTTTCTTTTC[-/T]TTTTCTTTTTCTTTT | 23092 |
| rs113911961 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206064 | TAATTAGGGCTATTA[C/T]TGGGTCTCATGTTTG | 23092 |
| rs113916834 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957198 | TTGATGAGGCTCTCA[A/G]TTGCTTTTGCAAGAA | 23092 |
| rs113917981 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816536 | GGAGATGCCATGTGC[A/G]CCCTGGGCCTTGGAG | 23092 |
| rs113929160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114714 | TGTGTTCTGCAGAAG[A/T]TGCATTCCAAGGTCA | 23092 |
| rs113942653 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782083 | AGTCAGCAGCATAGT[C/G]CCTGAGGAAGGGATG | 23092 |
| rs113952767 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817294 | AAGAGCAGGAGCAGA[A/G]TTGGCAAGGGACAGT | 23092 |
| rs113954817 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890327 | TTGGGCAGAATGAAC[A/G]CCAGGTGAAAAGGTT | 23092 |
| rs113983657 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903533 | AATAAAATTATTTTC[A/G]TCCTAGACAAGAAAT | 23092 |
| rs113998075 | snp | A/C/G | 0.0103333 | 0.0711729 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086749 | AAATTTTCTTGTCCA[A/C/G]CCTAAGTCCACATCT | 23092 |
| rs114002840 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863491 | TGCACAAGGAGACAC[A/G]CCATTTCTGGTTCTT | 23092 |
| rs114016711 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975730 | ACTTTATTACCCAGC[A/G]TCCCTGAGATTACTT | 23092 |
| rs114024337 | snp | G/T | 0.0573587 | 0.15934 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089516 | GGTGGTGTTTTGGGA[G/T]GAAGGTACAACACTG | 23092 |
| rs114025034 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905507 | TTACCCAGTGCATCA[A/G]TTTTTAACATTTAGC | 23092 |
| rs114032607 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031669 | TGACCTTATGGTTGT[A/G]TAGCAGTGGCAGTTA | 23092 |
| rs114038105 | snp | C/G | 0.0763149 | 0.179815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991071 | CAGAGGTGGAGTCTA[C/G]AAAGGCAGGCAGGCA | 23092 |
| rs114057962 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192147 | CTGCAATTCAATGTA[A/G]CATCAAGACGGGAAG | 23092 |
| rs114071890 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141552 | TTAAGTTATTAAAAA[A/C]AAAACTCCCTAATTG | 23092 |
| rs114071943 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016676 | CTATTGCACTCCATC[C/T]TGGGCAATAGACTGA | 23092 |
| rs114072890 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107493 | GCTGCCATCAGCTTG[A/G]CCTTCTTCACCCACC | 23092 |
| rs114082682 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132353 | AGAAAGACTGATGTG[C/T]CTAGGGCCACTCATG | 23092 |
| rs114084938 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792784 | GAAACGTAAGCTGGC[A/C]TGTGTTTCCCTGATG | 23092 |
| rs114084983 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198751 | AATTACTTACCATTC[C/T]TACTCACCCCATCTA | 23092 |
| rs114088250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777038 | TGAGCACCTTTTCAT[A/G]TGTTTGTTGGCCATT | 23092 |
| rs114090122 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815440 | TACACTGAAGGAGGA[C/T]ATTTCTTTTAAATGG | 23092 |
| rs114093824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185590 | CAAAAGCAAAAAATG[G/T]CTGCACACACCCTAA | 23092 |
| rs114107301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994740 | AAGATAATGATTATT[A/G]GCTGCTGTTTACTGA | 23092 |
| rs114108602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967947 | CTACTATTAAAGGCA[G/T]TGTTCAAAGAAGGGC | 23092 |
| rs114117367 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795244 | CAGAAACTCAGTTGC[C/T]TCAGTTTTCTCATCT | 23092 |
| rs114121229 | snp | A/G | 0.106987 | 0.205054 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103947 | GTATAATAAAAATAT[A/G]TATATATACACACAA | 23092 |
| rs114125012 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830125 | TCAGGAACATAGCAC[A/G]TGGGGATGTTATTCA | 23092 |
| rs114126903 | snp | A/C | 0.030665 | 0.119967 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862700 | CAATTTCCTCATCTG[A/C]TTGACTTCTCTGGCT | 23092 |
| rs114127587 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812160 | ATGAGGGTTGTTCGG[C/G]CAGACATCCTGACCT | 23092 |
| rs114129574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850250 | CCTCTTCCCATAGGG[C/G]TTATTCTCCCCATCT | 23092 |
| rs114134670 | snp | G/T | 0.0225045 | 0.103662 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058506 | CTACTTGTGTGTGTG[G/T]TCTAACCTTCCGTTG | 23092 |
| rs114137830 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079225 | AAGGATCTATAGAGT[A/T]GGGCAACCAAACAAG | 23092 |
| rs114142640 | snp | C/G | 0.00216981 | 0.0328664 | intron-variant, synonymous-codon | ARHGAP26 | GRCh38.p7 | 5:143057975 | ATGCAACCAGGCCAC[C/G]AAGCAGAGTTTTCAG | 23092 |
| rs114155640 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125080 | CATAAATATCTAAAA[C/T]TGGAAAAACATTTTT | 23092 |
| rs114164165 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883277 | CTTTTGGAGTTGCTG[A/G]TAAGGCTGGTGGGAG | 23092 |
| rs114190454 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151619 | TGAACTCTCCAGCCA[C/T]GAAAAGACATGGAGG | 23092 |
| rs114195571 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801322 | GAGTTATAGTCATAG[C/T]GAATAGAAATTGATG | 23092 |
| rs114200225 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821584 | CAGCACCATCAACAT[C/T]GTCTGGGAATTTGTT | 23092 |
| rs114200250 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876454 | AGTCTGGGTTCAAAC[C/T]CAAGTCTGCATTATA | 23092 |
| rs114201339 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902730 | GCCTGGAGGTTACAT[A/G]GTAGTCAGTGTTGTC | 23092 |
| rs114202519 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921142 | TCTGATCTAGTCCCA[A/G]CCTAGCATTTCACAT | 23092 |
| rs114208796 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048583 | AATTTTTATGATGTC[C/G]AGTCTGTTATCTTTT | 23092 |
| rs114217038 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013108 | CAAACAAATATCTAT[A/G]ATTGACTTTATAAGG | 23092 |
| rs114221382 | snp | A/G | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960501 | TGTCCAGTGCTGTCT[A/G]TCCATTAGTCACCTA | 23092 |
| rs114242834 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910428 | ATCATGTGATGTTGT[G/T]GTATATATTTTTTAA | 23092 |
| rs114257760 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177300 | TGGCTTTTGTTTGCT[A/G]CATAGTGCTTGTCAA | 23092 |
| rs114278974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218260 | CAGGGCCGTTGTACT[C/T]GCACTACCCACTGCT | 23092 |
| rs114280031 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920558 | GTTTACACTGGGGAA[A/G]GGAAATGATTACTTT | 23092 |
| rs114290057 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796686 | CCCTGTGGACTCTGG[C/G]CCCTGCCAGCTCCTC | 23092 |
| rs114291000 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859726 | TCCACCTTCAGCGTA[C/T]GATGTGTGAGGAGGG | 23092 |
| rs114291381 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028566 | ATATTGGTAATACTA[A/G]GTAATATTGGTCATG | 23092 |
| rs114310053 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167418 | ACCCGGGGGGGAAGA[G/T]GTTACAGTGAGCTGA | 23092 |
| rs114311721 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091481 | GTCCTTGGTACCTTT[C/T]TACTGAGAAATTTCC | 23092 |
| rs114319655 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941604 | ATTTAGGTGGACTTC[A/G]TAATAGGTGCATATG | 23092 |
| rs114328030 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211713 | CCTGGACTCCACACG[A/T]GTCCCATCATGCCTG | 23092 |
| rs114336844 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871825 | ATTTTGGTAAGGACC[A/G]TTCTGTGAAAGTGAC | 23092 |
| rs114341532 | snp | C/T | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009045 | TCAGAATTGCAGTGC[C/T]CTGTGATTTGTATCA | 23092 |
| rs114345162 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974585 | TTAACTCATGTAAAG[C/T]GTTTGTGGTTCTCAT | 23092 |
| rs114353172 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931335 | GTCTCTTTTTCTTGC[A/G]GAGTACCATTTGTGA | 23092 |
| rs114362328 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824434 | GGCTCAGTACTTACT[G/T]GTTTAGCTGACATCC | 23092 |
| rs114363252 | snp | A/G | 0.084364 | 0.187256 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159597 | ATTACCAACATCTAG[A/G]CCCCTTCCCTGGAGC | 23092 |
| rs114366415 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168073 | CAAGGAAGGCTTTGT[A/G]ATCAAATTGGCACTT | 23092 |
| rs114368038 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214881 | TCCCTTTTATCGTTC[C/T]CAAAGCCTCAAGCAC | 23092 |
| rs114374231 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154746 | AAGATTTGGAAACCT[C/G]TGAATCCCACAGGGT | 23092 |
| rs114377552 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179369 | AAGAGAGCTGTGGGA[G/T]CCCAAGTGAAAACAG | 23092 |
| rs114398359 | snp | C/T | 0.0236746 | 0.106192 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:142920034 | ATCACTTTTTTTATT[C/T]TTTAATGAAGCAGCA | 23092 |
| rs114401870 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918064 | AAATTAAGTGTTAAT[C/T]CAGGCCAATGGGATT | 23092 |
| rs114403209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792638 | AAATCTCTATCCCCA[C/T]TGACTTCTCAGTTGG | 23092 |
| rs114406431 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888110 | TGGGTATGGTGTTAA[G/T]CACTTTACATGGAAT | 23092 |
| rs114412111 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101838 | GGAGAAGGGAAAGTT[C/T]GTCATATGACATAAA | 23092 |
| rs114414184 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089485 | GTAATGCCTTTGTTA[C/T]ACTTCCATCAGGGGT | 23092 |
| rs114425063 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011278 | GAGAGGCATTTCCTC[A/G]CCTAAAGTCCACAAT | 23092 |
| rs114430889 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964795 | AGCCTCACAGGGTCG[A/G]TGGGCTTCTCCCTGT | 23092 |
| rs114431829 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014329 | AGGCTGTAGTGTAGT[C/G]ACACCTTGCATTGAA | 23092 |
| rs114443659 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137125 | AAGAACACGACTTCA[A/G]TGGTCTCACTGTATT | 23092 |
| rs114454031 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956968 | GTCCCTCCCACAACA[C/T]GTGAGAATTTTGGGA | 23092 |
| rs114459915 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101140 | GTTCTGAAGCCATTC[C/T]TCACTTGAGAAGCAT | 23092 |
| rs114489839 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952648 | TTTACTCTTTGGGAG[A/G]TCAGTCATCCCATTA | 23092 |
| rs114534769 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799724 | CAAAGAGAGGATGAG[A/G]GAGGCAAAAGGGAGC | 23092 |
| rs114543421 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877060 | GTGGGGGTGTGGCAA[A/G]CAAATCACCATGAAT | 23092 |
| rs114543599 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979923 | CCTTCAGAGAGGAAT[A/G]TCACCTGGAGTGGAT | 23092 |
| rs114544220 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843066 | AGGTGGACCTACCCC[A/G]CCTTTGGCAACTTCT | 23092 |
| rs114544610 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779730 | GAGACTTCAGATAGA[A/T]CTCCAAGCTGACTGA | 23092 |
| rs114545010 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820512 | TCCTGGAGCTGAAGG[C/T]GGTAGAATAACTTCA | 23092 |
| rs114551836 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769722 | GCTAGATGCAGAGCA[A/G]GAAAATAACAGGCGG | 23092 |
| rs114560480 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201560 | TTTATTTTTGTCTGC[C/T]GTTGTCATTTTTAAG | 23092 |
| rs114560726 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219677 | TCCTCTATTAGTAAA[C/T]GACAATTTGCATTTT | 23092 |
| rs114566472 | snp | A/G | 0.00213521 | 0.0326044 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772827 | GGACTTGTGTTTTCT[A/G]TTTTGGCATTGAATC | 23092 |
| rs114567022 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165042 | GAATTTGTAGTAAGT[A/G]AGAGAAAGAAAACAC | 23092 |
| rs114567471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804144 | TATCAAATATTGCAA[A/G]TATAGGTTGAATCAT | 23092 |
| rs114570127 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791079 | GGTTTATTTTGCTTT[A/G/T]AAGTTTTTTTTTTTT | 23092 |
| rs114573137 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893858 | TGAACGTTTTTTAAT[A/G]TACCCTTTGGCTATT | 23092 |
| rs114575943 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081241 | GGAGAGGAGCCAGGA[A/C]AGAGTCCTGGGGCTC | 23092 |
| rs114579776 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034637 | GGGAGGAGGGCAAAA[A/G]TGTTCTGGAGTTAGA | 23092 |
| rs114583860 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909583 | TGAATCAAAGCAATA[A/G]CAAAGCCCTTTTTAT | 23092 |
| rs114591033 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147705 | TTTACAAACGTCCAG[A/G]GACTGTAGCAGCTCT | 23092 |
| rs114597961 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809358 | GAAGCCAGGATGTGA[A/G]GGACTTTGAGCTTCT | 23092 |
| rs114598058 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201239 | ATTGGGCCTAGATGT[A/G]GGGGCCTGGCAGGAC | 23092 |
| rs114606458 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010220 | CTGGAGTGACTTGGT[A/G]GTGATATACATTTGC | 23092 |
| rs114607566 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053252 | AGGCACTGAGTCCAG[A/T]GAGTTGATATACTTT | 23092 |
| rs114620272 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855070 | GCACTAGATAAAAGA[A/G]GAATCACAAAAATAA | 23092 |
| rs114641556 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220730 | TAGTGATCTGAAATT[A/G]GCCAACTTTGGAGGC | 23092 |
| rs114654708 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903131 | TAAGGAGGGACTCAT[A/C]TGTGAGCCATCAGCA | 23092 |
| rs114655308 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173247 | GAAAATAAATATGGA[A/G]TGCCCTCGAACTCTT | 23092 |
| rs114658936 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943494 | TCTCTGGAGCTTCTT[C/T]TATGAGGGCACCCAT | 23092 |
| rs114660918 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159548 | TCTCAGTCCAGATGG[C/T]ACATCAGCACCACAT | 23092 |
| rs114681191 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055530 | AGCAGGTAAAATTTG[A/T]TTATATCATACCTAA | 23092 |
| rs114683575 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221005 | TAGGGGAAAATCTAT[C/T]CTCTCCAAATAATCT | 23092 |
| rs114695984 | snp | C/T | 0.0134861 | 0.0810011 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223459 | TGCAACTGATGTTTG[C/T]TTTTTAAAGGGTAAG | 23092 |
| rs114710470 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065232 | ATTGGCCTTGGGAGC[A/G]TGTTCTTCATGAAAT | 23092 |
| rs114712195 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825848 | GTGTCCTTGGCGGAA[C/T]CCCTCAGAACACAGT | 23092 |
| rs114721979 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082316 | TCTGGACTGTCACAA[A/G]AATATGGAGTTGTGT | 23092 |
| rs114722592 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199287 | AGGTTAGGACTTATA[C/T]AGGATTTCTTTGTTG | 23092 |
| rs114730480 | snp | A/G | 0.202343 | 0.245416 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012578 | ATATATATATATATT[A/G]TGATCAGGTTCACCT | 23092 |
| rs114738784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868588 | GACTTGGGAATGGAC[A/G]TGGCACATGAGGGAG | 23092 |
| rs114742987 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931029 | TACTCAGACAGGAAT[C/T]GGACTTTAGTTCTTG | 23092 |
| rs114760932 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124959 | GCTTTTCCGCCTCCT[C/G]TCTGCATTGCCATTT | 23092 |
| rs114763769 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089669 | TAGTGTAGTTAGTAA[A/G]TCACTGTTGGTTGTA | 23092 |
| rs114765533 | snp | A/C | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228518 | GCAAGAAAGATCAAA[A/C]CCATGAATGCTTAGT | 23092 |
| rs114782187 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056923 | GAGCGAAGATGGTGT[G/T]TATGTCATTTCTTTC | 23092 |
| rs114782343 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034398 | TGATATATCTGGACC[A/G]TGGAATATTATTTAA | 23092 |
| rs114783012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876303 | GAACACTATTCACCA[A/G]GATGCATTTTCTATT | 23092 |
| rs114783994 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902415 | GTGGAGTGTGTGTTC[C/T]GGGAATGGGGGCTGG | 23092 |
| rs114811941 | snp | A/C/G | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785466 | GGCCTCTGGTTTCAC[A/C/G]CTTCTTTTGTCTTGT | 23092 |
| rs114817633 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157100 | TAGAGATGTCTAAAT[C/T]AGCATTTCCCAAACT | 23092 |
| rs114825108 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181434 | CCTTTCCTGCTTCCC[C/T]CTCCTTACACCTTCC | 23092 |
| rs114828471 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215907 | TGCTTGAATAATGCT[G/T]CTGTGAACATGTGTG | 23092 |
| rs114835505 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853011 | CAAGCTTGCCTTTAT[C/T]GAGCTCCAAAGGTGG | 23092 |
| rs114838556 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915896 | CTGGGAACTCTGCCC[A/G]GAATCCTTTTCTCTC | 23092 |
| rs114844534 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983028 | TGCCTGGGATTGCTG[C/T]GCTTGCCCAGCCCGC | 23092 |
| rs114850719 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803616 | CCTCACGCTATTGCC[A/G]AACATGCGACAAGGA | 23092 |
| rs114893238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871845 | GTGAAAGTGACTGAA[C/T]GAGGGAGAGATCGGA | 23092 |
| rs114895301 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849502 | CATTGACAGTGTGCT[C/T]TCCATGCTTCATTCA | 23092 |
| rs114896692 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066369 | ATTGTTAAGCGATGC[A/G]TGACTATACTTCAAG | 23092 |
| rs114904279 | snp | A/T | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960776 | CAGACCTCTGGTGTG[A/T]TCAGAAAGGCAGCCC | 23092 |
| rs114932767 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081513 | GTCCTGGAGTCAAAC[A/T]GACCTGAGTTCAAAT | 23092 |
| rs114938849 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006965 | CTGGGCACAGTGGCT[C/T]ATGCCTGTAATCCTA | 23092 |
| rs114940327 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062635 | AGAAACAGTGAATTG[A/G]GTTCATATACAAATG | 23092 |
| rs114942661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820748 | TCATAAAGGCCATAA[C/T]AATAAAACATAAGAA | 23092 |
| rs114946262 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028636 | ATTTCATTTGACCCT[C/T]GTAGCATCCTGTTGA | 23092 |
| rs114950378 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211042 | AAGCCTACAAATACA[A/G]TCTCTCTGCCAACAG | 23092 |
| rs114955589 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889792 | AGGTTGTGAGTGTGT[C/T]GCAAAATCACAGTTT | 23092 |
| rs114957877 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910879 | CATACATGTTTGAAC[A/G]GAGCTCTCCTAGGAG | 23092 |
| rs114959473 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962985 | TAGGCTCCAGTGTCT[G/T]TTGTTCCCCTCTGCG | 23092 |
| rs114960720 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858748 | CACACTCAAAGAGAT[A/T]ACCAATTGAAGGGAT | 23092 |
| rs114962638 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931317 | GGTCGTTTTTATGGC[A/G]CAGTCTCTTTTTCTT | 23092 |
| rs114979802 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852575 | GGCTTGTAACAGTCG[A/G]GATTTCTGTTCACAT | 23092 |
| rs114983287 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980807 | TAGTAAATATTGCCA[C/G]ATAGTCTTGCAAAGA | 23092 |
| rs114986288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778742 | TTCCTTCAAGTGGAA[C/T]GGTTGCTGGCTCCAG | 23092 |
| rs114990292 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939182 | TAATTGGTTGATCTC[A/G]GATAGATGATTCAGG | 23092 |
| rs114995052 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201463 | CCAGGAGTGAAATTG[A/G]CCATTTTGAAATTTG | 23092 |
| rs115002220 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211246 | TTGGATGGTAGATAA[A/G]CAACAAAAATTTTTT | 23092 |
| rs115011009 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115564 | GGCAGGATACCAAGC[A/G]AAACTACCAACTAAC | 23092 |
| rs115030773 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998044 | GGAACCAGAAGCTTG[A/C]AGGAACCTAACTGTG | 23092 |
| rs115038875 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832895 | TCTTTCAGCTCAACA[C/T]AGTTCAGTTTTTTTC | 23092 |
| rs115041910 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973520 | ATAGAGAATTTTAAC[C/T]TTCCATTTTTAAACT | 23092 |
| rs115043490 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800445 | CGTGATCTCGGCTTA[C/T]TGCAACCTCCGGGTT | 23092 |
| rs115056565 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878162 | TTTCATTGCAGTGGA[C/T]ATGCATGTGGTTTAG | 23092 |
| rs115065252 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142959202 | GTGGACATTTGTACA[A/G]ATGATAGAACAAAAG | 23092 |
| rs115068781 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871455 | TGGGGGAGGCACAGG[A/G]TTGTCGGGTGGGTAG | 23092 |
| rs115069354 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210730 | GTGCCATATGATGGC[A/G]AATGGGTCATCATTT | 23092 |
| rs115073033 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944061 | TCTTTGTCATTGGCA[C/T]TAGTTGCAATTATGT | 23092 |
| rs115074551 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035341 | TGGTGTATATATATG[A/T]TGGATTACTACTGAG | 23092 |
| rs115077265 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061862 | AGCAGAAAAGGCATT[A/G]TTTCTTCTCTGAGTC | 23092 |
| rs115078521 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002059 | TGTGGGGATGAAGGC[A/G]ATCATGAACGTGCTT | 23092 |
| rs115090545 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153281 | TAGGTTTTAGTTCTG[A/G]CATCGACATTGCCTG | 23092 |
| rs115091056 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889212 | CAATTCATTCATTCT[G/T]CATGCATCTGTTGAA | 23092 |
| rs115093089 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853471 | GCTAGGATTATAGAC[A/G]TGAGCCACTATGCCC | 23092 |
| rs115094409 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099184 | CTTAGTTTGATATCT[A/G]TCTTTGCAGAAGCTG | 23092 |
| rs115110998 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166651 | AGAATTTCACCTGCT[A/G]CTTTGCTAAATTCTC | 23092 |
| rs115111223 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857689 | TTCTTCTCTCCTCTG[A/G]GAACAGTTTCCTGCT | 23092 |
| rs115112054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833531 | AAAGAATATGATGGA[C/T]ATTTTTGTATGTACT | 23092 |
| rs115132962 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052979 | GTAAAAAGACGGAAA[A/T]CCTGACCTCACCTGG | 23092 |
| rs115137146 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016433 | CACTTTTGCCAGCAC[A/G]GTGGCTCACGCCTGT | 23092 |
| rs115138151 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198618 | CCAATCTGGAATTTT[C/T]CCCTCTACCTCATAT | 23092 |
| rs115140719 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086748 | TAAATTTTCTTGTCC[A/C]GCCTAAGTCCACATC | 23092 |
| rs115153046 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110408 | TGCTGGGTCACCTTG[A/C]ACTTTCTTCGTTGGG | 23092 |
| rs115153987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150162 | ACTCCTGAAGTAGCC[A/G]TCTCTCCTGAAGAAC | 23092 |
| rs115158762 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142919079 | TCCCTGCCAAAATCA[C/T]ATGCTGAAGTCCTAA | 23092 |
| rs115159237 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053313 | CCCCTGGAAAAAGTA[A/T]GAAAAGGGTTGCTCT | 23092 |
| rs115198172 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773322 | TATAGCTCTAAACTT[C/T]TGTGGCTTTATTTTA | 23092 |
| rs115202362 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997152 | ATATTGTATGTGCAT[A/G]TATATATATATACAC | 23092 |
| rs115209447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921044 | GACTTTCTTAACAGA[A/C]CTCATCTGATTTTCT | 23092 |
| rs115221728 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067325 | TGTGAAAACGGCCCT[C/T]TTGACCTTCCAGTTT | 23092 |
| rs115233191 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896288 | TCTTTATATATACTT[C/T]GATTAATATTATTCC | 23092 |
| rs115252728 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030322 | GAGTTAGTGTAATAT[A/G]GAGAAGCCCTCCTCT | 23092 |
| rs115253654 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131475 | AACCAGGCCTATCGC[C/T]AACTCTGAATTCATT | 23092 |
| rs115254590 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055107 | GTTATTGACCAGCTG[C/T]CTGCATCTTAGTTTC | 23092 |
| rs115258970 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012114 | AGCGTTTAGGTATAT[G/T]CATTGATGCCTTTTC | 23092 |
| rs115265291 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835905 | CATCACAAAACCCTC[C/T]AAGATTAGTTTTAGT | 23092 |
| rs115270716 | snp | A/C | 0.0333238 | 0.124705 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199631 | ACCACCTAACAGTCT[A/C]ACCTGGAAGGGGAAC | 23092 |
| rs115279892 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026763 | TGTTTTTAAAAGATG[A/G]CTCTGGCTGCTGGTG | 23092 |
| rs115279937 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783963 | CCCTGCTGTGGACAA[C/T]ATGTCATTGTGGAGG | 23092 |
| rs115290105 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813530 | GGTCCCACAGACAGG[A/G]CAGTTTCAATAACAA | 23092 |
| rs115291866 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926093 | GTTGTGATTCTGTTT[C/G]CTCTTGGCTGGTGAG | 23092 |
| rs115293134 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789757 | CAGACTCGAACACTT[A/G]GGCGGTTCTGGGGTA | 23092 |
| rs115305253 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193649 | TGCTAAAGAGAAGCC[A/G]TAAAGTGCTTCCTGT | 23092 |
| rs115320914 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950600 | TTGTTATCAGAATGT[C/T]ATGTTTCCTACAGCG | 23092 |
| rs115322093 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855028 | TAGAGTCAGCTCTGG[G/T]TCCCTCAGAGAAAAG | 23092 |
| rs115335236 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897353 | ATGCTGAGAGGCTGG[A/G]TATAGGATTCAGATG | 23092 |
| rs115356299 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884943 | ATAGGTACCCCCACT[A/G]CTGCTGCTCCCCAGC | 23092 |
| rs115359613 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921103 | GCAAGCTTTCCATGA[A/G]TAGGTAAAGGGCAGT | 23092 |
| rs115365072 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907438 | ACCTTTACTTCCGTT[A/G]TATTTTAAGACCCAC | 23092 |
| rs115371922 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949540 | GTAGGCTGTTTCCTT[G/T]GATAGGTATCAGTAT | 23092 |
| rs115377971 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197273 | GAATGGTATCTTCAC[C/T]TTTGCTAGATAATGC | 23092 |
| rs115378222 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067884 | ACATAAAAACAGGGT[C/T]CAAGAGCAGTGGCTC | 23092 |
| rs115379190 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181646 | AACATTTATTTATAC[A/G]TGACATGAATGAGTA | 23092 |
| rs115386119 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215916 | AATGCTGCTGTGAAC[A/G]TGTGTGTAGGTTTTT | 23092 |
| rs115390691 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813077 | TGAGTAGCTGGGACT[A/G]TAGGTGCCGGCTACC | 23092 |
| rs115401506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825321 | GAGGAAGAGGGTAGT[G/T]GGGAGCCCACTCAGG | 23092 |
| rs115402280 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865156 | GTACCTCAGTTCTCT[G/T]TGCCAGGGCTGAGCT | 23092 |
| rs115411016 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891277 | AGTAAAGATTCATCA[A/G]TGCTCAGATATCTCC | 23092 |
| rs115416869 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878565 | TGTGTGTGTATAAAT[A/G]TGTAGTGTGTAGTGG | 23092 |
| rs115418783 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931568 | CTTCTCCATGTCTGA[A/G]GCAGTTTAGAAGCAG | 23092 |
| rs115419735 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939107 | AAGAAGCAAGCCCAC[A/G]CGTAAGTCAATATCA | 23092 |
| rs115446993 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075090 | GATAGCCTAAAGCTG[A/C]ATGTTTTCTGTGCTG | 23092 |
| rs115451042 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165160 | TTTTTACACATCACC[A/G]TGGGGCTGGCCTGGT | 23092 |
| rs115453336 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081003 | AATGAGCTAGATGTG[A/G]TATGTGTAGGGAAGG | 23092 |
| rs115455454 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825202 | GGTTATGTATTGAAA[A/G]TGCTTACAACAGTAC | 23092 |
| rs115455783 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775655 | TCCCCTCCCCCAACC[C/T]TAGTAACCTCTATTC | 23092 |
| rs115468685 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168709 | GTTGCCTTGGAGTTA[A/G]GCTATATCTCTAGGA | 23092 |
| rs115472900 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051510 | AAATGACGTCTCTGT[A/G]GCATATTCAGATGCC | 23092 |
| rs115473737 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951598 | GGGTGGTAGTATGTC[C/T]GTCTTGAGGATCTTA | 23092 |
| rs115473945 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212547 | TGGTGAATACTAAGG[A/G]CTCTTCTTTCCTTTG | 23092 |
| rs115479954 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033923 | AAAACGTAATTCCCC[A/G]TCTGACAAATGCTTT | 23092 |
| rs115480080 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014400 | TCTCCTTTAATCGTA[C/G]GTCTTAAGACTATAG | 23092 |
| rs115480376 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119643 | GTGGACCAGAAACAG[A/G]CCACTCTCCCTGCTG | 23092 |
| rs115496167 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173524 | TTTTATTAGTAAGAG[G/T]CAACATTTCCGAATT | 23092 |
| rs115516571 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122678 | AAAAGCAGATTAATT[A/G]TTTTGAAGTTACTTT | 23092 |
| rs115520132 | snp | C/T | 0.11228 | 0.208646 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022364 | AGGCATGAGCCACTG[C/T]GCCTGGCCAATCCCC | 23092 |
| rs115528776 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007774 | TGGTGTTTGGCACAT[A/G]ATTGATAGTGAAAAA | 23092 |
| rs115531078 | snp | C/T | 0.0115144 | 0.0749975 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229101 | AAAGGTCACAAGTCT[C/T]GGCTCCTGCGGTTTT | 23092 |
| rs115531551 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981644 | CTTGGCTCCTTTCCT[A/G]CAGAGCAGAATTATC | 23092 |
| rs115531612 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888607 | GCAGGGTTCTGCACG[A/G]AATGCTTTTAAATTC | 23092 |
| rs115533095 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165493 | CAGTATTAAGAGCTT[A/G]GGTTCTGGGGGCAGA | 23092 |
| rs115533323 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201811 | TGCAGTACATAAAAT[A/G]TGCAGTAGTATTGTT | 23092 |
| rs115533402 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947620 | CTGTGAAACATAATA[A/G]GCACCTATTACTCAC | 23092 |
| rs115542403 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027937 | GTGCACTCTTGTTCA[C/T]TGGAGTTGAGAGCCG | 23092 |
| rs115564855 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898380 | TGTTGCCTGAGTTTT[C/T]GTAATTGAAGGTTGG | 23092 |
| rs115566115 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862254 | ACCCTGGAAGAGGCA[G/T]GCCTAAGGATGTGGA | 23092 |
| rs115573619 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080953 | GTGGGCACATTTGGG[A/C]TATATTTTTAAAGAT | 23092 |
| rs115574572 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962240 | TGAATTTTACCTTGA[C/G]AAATTTGAAATTGTG | 23092 |
| rs115575466 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790381 | GTATTTTTTCCCATC[A/G]TATTTCTCCTGTTTT | 23092 |
| rs115589333 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190471 | ATACATTGAATTTTC[A/G]AAGTGCTTAAGGAAA | 23092 |
| rs115594710 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225877 | CTTCCTATTAGCTAC[A/G]AAACTGGATAAACTT | 23092 |
| rs115620986 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828965 | TGTTTCACCTGTTAA[A/G]GTGTTTCTGTGTGCT | 23092 |
| rs115623018 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849517 | CTCCATGCTTCATTC[A/G]TCCCCTTCTGAACGT | 23092 |
| rs115638139 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205941 | GTTCTAAAAATATAC[A/G]TAATGGAATTTAATA | 23092 |
| rs115653794 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808744 | TGTTTGGGACTAGGG[G/T]TGAGCTCCAAGATGG | 23092 |
| rs115654052 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889481 | AAATTAGCTAGATGT[G/T]GTGGCACGCGCCTGT | 23092 |
| rs115663005 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868640 | ATGTACTGGTGACTT[A/G]TGCGGCAGGGTGAAT | 23092 |
| rs115665811 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120090 | CAGGTGATTTAGGGA[A/T]GCTCTTGATATTGTC | 23092 |
| rs115667759 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814591 | TCTTCAGTACAACAA[C/G]GTGAGATAAACAAGT | 23092 |
| rs115668148 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778374 | GTATACAGTGTAAAA[A/G]CACCCCCTTTTCCTA | 23092 |
| rs115670685 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191450 | AAAAGGATTAGTGGC[C/T]GAGAACAGAAATTTC | 23092 |
| rs115677074 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852171 | AGTGAGGTATGCAGC[C/T]GCCGGCAAAGCATCA | 23092 |
| rs115683216 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940226 | TAAGTGATTGAAAGA[A/G]TATGGATAGTTAGGA | 23092 |
| rs115688610 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226915 | TGTGTGCCATACCTG[C/T]GGCTCAAAGGGAAGG | 23092 |
| rs115689786 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973218 | TAGATAGAAGAGATC[A/G]TTAAAAAGGCATTGC | 23092 |
| rs115697407 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793836 | CAAGCGATCTGCCTG[C/T]TTCGACCTCTCAGTG | 23092 |
| rs115697432 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861923 | ATACCTTGTTTTTCT[C/T]TTGATTGCCCTCAAA | 23092 |
| rs115698250 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777022 | TGGTGACCAATGAGG[A/T]TGAGCACCTTTTCAT | 23092 |
| rs115701788 | snp | A/G/T | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874513 | TGGCTCAAGGGTCTC[A/G/T]AGTATCCTCAGGGCC | 23092 |
| rs115702281 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912434 | GATGGATTGCCAGGG[G/T]ATACAAGGAAACTTT | 23092 |
| rs115714515 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031082 | GAGCCAAAGGCTCCC[A/G]TGCGAAATCCACAGT | 23092 |
| rs115733799 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924217 | CTTCCTCCCTCCCTC[C/T]TCTTTCCAACTCTCC | 23092 |
| rs115735591 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958168 | ATTTCCCTTCCCCCC[A/G]TTTCTCCTCCCCCTG | 23092 |
| rs115736212 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930244 | GGTCTTTAGAGAAAG[G/T]TGGAAGGGTGGAATC | 23092 |
| rs115807751 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152152 | ATGATGCTGGAATGG[C/G]ATATACACAAGACAT | 23092 |
| rs115808418 | snp | C/T | 0.096524 | 0.197345 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768389 | ATGTTCACACTGGAG[C/T]CTTAAGGCTGCCATA | 23092 |
| rs115813255 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807698 | TGTTGCAACCCTGGC[C/T]CCTAAGCCTGAGGAC | 23092 |
| rs115813769 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112776 | TCATCCATGTCATAG[C/T]ATATGCTAGAATTCC | 23092 |
| rs115815346 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108310 | TACTATACCAGTAAT[C/T]TTCATGGATGTTAGA | 23092 |
| rs115816201 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794874 | GTCTCTTTCTCTTTA[C/T]GATATTTACATTTTG | 23092 |
| rs115833345 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196026 | CACCCAGGGAATGCT[A/G]CTAATATGTTAAGGT | 23092 |
| rs115834907 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188903 | GCTAGAGATGTGGCA[A/G]GTTACACAGAAGAAG | 23092 |
| rs115841406 | snp | C/G/T | 0.00337514 | 0.0409523 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222511 | TGCTGATTCCAGTGT[C/G/T]GAGGCCATTTCTCTT | 23092 |
| rs115844879 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816431 | TAGAGAACACAATTA[A/T]ATAGTGCCATAGGAG | 23092 |
| rs115850993 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179374 | AGCTGTGGGAGCCCA[A/G]GTGAAAACAGGGACT | 23092 |
| rs115857047 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023655 | GAGGCTGCCAGGCCT[C/T]TGCTGGTCGGTGGCT | 23092 |
| rs115868694 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178319 | TGGCAGTCTTAACCT[A/G]TAAGCTCCTGTTCAA | 23092 |
| rs115871725 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183713 | GTTATGGGCGAAGGC[A/G]TACCAGGGGAATGGC | 23092 |
| rs115877287 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863771 | CTGCTGGATCACATG[A/G]GAATTTTGACAAGAT | 23092 |
| rs115880460 | snp | C/T | 0.000614174 | 0.0175131 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054436 | GTCTTTTCTTCATTT[C/T]AGACCCCAAGACTGC | 23092 |
| rs115886842 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975112 | TCTTACACATGGGGT[A/G]GTCGAGGAGGGGAGG | 23092 |
| rs115891491 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010006 | AATTTGAGATTGCTA[A/G]TCATAAGACAAAGCT | 23092 |
| rs115907260 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115923 | TTGCACTTTATACCT[C/T]TATAGCAGTATTTCT | 23092 |
| rs115910851 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896326 | CTTGCTTTTGATGAG[A/T]TTTTTTTGTAATTGG | 23092 |
| rs115926027 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979672 | AGAAGTGGAGGCCCC[A/G]GCTTCTGTTCTGGCT | 23092 |
| rs115930485 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777720 | TTTGGATGGAGGTAA[A/C]CAATGTAGGAGTCAT | 23092 |
| rs115952801 | snp | A/T | 0.0513262 | 0.151752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983514 | ACCAGCCTGGTCCTT[A/T]GTTTCTATTGTTTTC | 23092 |
| rs115959038 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152399 | TAAAAAATAGAGTCT[A/G]TTAACACATCTTTTT | 23092 |
| rs115979745 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227025 | CCAAAAGCATTCACA[A/G]TTGAGGGGGAGAAAG | 23092 |
| rs115983253 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072496 | AACCAAAATATGGTA[C/T]CAACCTATGTGTCCA | 23092 |
| rs115989904 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105650 | CTTGGTACAGGTCTC[A/G]TAGCCTTGCAGCACT | 23092 |
| rs116009054 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832969 | AAACTACCTGTATCT[A/G]TAGAATATTTGAAAA | 23092 |
| rs116017741 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912604 | TTTATTGAGGAGCTA[C/T]TCTTTTCTAGGATCC | 23092 |
| rs116020813 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069382 | TGAATGAGTGGAAAA[C/T]ATCCAGGTAACTCAT | 23092 |
| rs116022158 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091057 | ATGGTCAGCAATAGA[C/G]CGAGTAAAGAAAAAA | 23092 |
| rs116022278 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060155 | GTTTAGACTTACCCT[A/T]GGCTATGCCTGAGCT | 23092 |
| rs116028299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033995 | TCCTCCCTGCACATG[A/G]AAAGATTCCCAACAT | 23092 |
| rs116028318 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975225 | GGAAAAGCTGCTCAC[C/T]CCTCCTAGGCCTGTG | 23092 |
| rs116028946 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783002 | AATTTCCTATACCCC[C/T]GCCCCCACTCCCTTC | 23092 |
| rs116034297 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908582 | GTAGACACTGCATTG[C/T]CTTTTCATGACTTAA | 23092 |
| rs116035556 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813747 | AATGACCTCATTTGC[A/C]TTAATTACCTCTTTA | 23092 |
| rs116044894 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160489 | GGTTTTTTTTTCTTT[C/T]TTTTTTTTTCTTTTT | 23092 |
| rs116065810 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787296 | CAAAGTAGGTCAATA[A/G]TTTATATTTCAAGAA | 23092 |
| rs116066988 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826385 | TGTTAGGAATTGTCA[C/T]ACTACCCATTTTGCA | 23092 |
| rs116067848 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860148 | CACATGCTCCACTGT[C/T]GCACTGGATCTCACT | 23092 |
| rs116068783 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884742 | AACAAATGTGTGTGA[A/G]GATAATATTGTTGTT | 23092 |
| rs116071147 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923203 | GGTGATTGAGGCAAC[C/T]CTATTTTTACTCTTT | 23092 |
| rs116088779 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003635 | GTAGGAGCAGTAAGA[A/G]ATCAAAGAAACGAGA | 23092 |
| rs116101547 | snp | C/T | 0.00166265 | 0.0287847 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879367 | TTACTCTGTTGTTCT[C/T]CACCAGATTGAGAAT | 23092 |
| rs116115299 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220393 | CTGTACTGAGCATTT[C/G]CTCTGTGCCTGGCTC | 23092 |
| rs116122557 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215621 | TAGCAGTCATGCCCC[A/C]CTTACCACAACCCAT | 23092 |
| rs116124038 | snp | G/T | 0.0115288 | 0.0751856 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830817 | ACTCAGCCAGACTGC[G/T]CCGTATCCCCCTCTC | 23092 |
| rs116138083 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191706 | GTTTGGGCGCCACCA[C/T]CCAGTAGCCAGGAGC | 23092 |
| rs116141049 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158435 | AGCCAACTGGAAACT[A/T]CGCTGATTAGGCTAG | 23092 |
| rs116143930 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131291 | ATTTACTACAGTTCT[C/T]AGGAAATAGTAAAAG | 23092 |
| rs116158289 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802173 | ATTTTGCCCCATCCT[A/G]TTATCATTGGTGATG | 23092 |
| rs116178229 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001807 | TGGGGATACCCTTTA[C/T]TGCCAGCTCAAAGCA | 23092 |
| rs116183241 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772672 | TTACCTCTGAGTCAC[A/G]CAGCTCTAGCAGCAG | 23092 |
| rs116200657 | snp | A/G | 0.039522 | 0.134904 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794312 | CAGTGGGTAAAATAA[A/G]TGTTCTGAAAGTCAG | 23092 |
| rs116219707 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812423 | CTCAGTGCAACCTCT[A/G]CCTCCTTGGGTTCAA | 23092 |
| rs116225661 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926803 | CTGCCCTTCTGCAGC[C/T]GTAATTTTAACCTTA | 23092 |
| rs116227684 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219127 | GTTAAATAGAGGCCT[A/G]ATACAGTGGGAAGGG | 23092 |
| rs116232609 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058603 | CTAAATTATTAAACC[C/G]TACATTCTATTGAAC | 23092 |
| rs116235218 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142647 | TGGCTTGGCATGTCA[C/T]TATTATCAGGAACAA | 23092 |
| rs116253715 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943516 | GGCACCCATCCCATT[C/T]ATGAGGGCTCTGCTG | 23092 |
| rs116258002 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055163 | GGACTTGAAGGACAG[G/T]AATACCATAGTTCTT | 23092 |
| rs116259204 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115743 | TCAAGTTTACAAGCT[A/G]CAAGCTACATATTAT | 23092 |
| rs116282729 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864900 | TTGCGCAGCCAATGC[A/G]CGTCATACGCCTCTG | 23092 |
| rs116286517 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039502 | ATGAGCCACTGTGCA[C/T]GGTCTAACTTTCAAC | 23092 |
| rs116296283 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871110 | CAGTCATTACCTAAT[C/T]GTCTATCGGGGGATC | 23092 |
| rs116300342 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921953 | GTGAGCCTGCTTTTT[C/G]TCTTAATGGTGCTCC | 23092 |
| rs116308181 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197907 | TAGTAGCATAAAATC[A/G]TATAGGCCCATGATA | 23092 |
| rs116311421 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809668 | GCAGATAGAGAGAAA[A/G]TAATCTTACAGTCAT | 23092 |
| rs116312825 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814587 | TAAATCTTCAGTACA[A/T]CAAGGTGAGATAAAC | 23092 |
| rs116313512 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778167 | AAGTCTAGAATGATT[C/T]AGATATTTTTGGCCT | 23092 |
| rs116319276 | snp | A/G | 0.0644444 | 0.167538 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034502 | TAGACATAAAAGACC[A/G]CATCGTGTATGATTC | 23092 |
| rs116320430 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934735 | ACTTCTATCTCAGTT[G/T]TTCTTTGATGGATTA | 23092 |
| rs116322396 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908051 | ATATTTTTGTATTTC[A/G]CATATATACAATATC | 23092 |
| rs116329953 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822899 | GAGACCAGTCAGTAA[A/G]TAGTTGCTGAGTGAT | 23092 |
| rs116331823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867579 | CTCTTCCTTAAACCA[C/T]TTTAACTGCAACCTG | 23092 |
| rs116336830 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973062 | ATTTGGGGTTGTTTT[A/G]GATTGGTAATTCCCC | 23092 |
| rs116336834 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946242 | TCTACCCTATCTACT[C/T]ACATCATATATTCTT | 23092 |
| rs116360586 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130896 | AGAATGTGTAATAGT[A/G]ATTATGATAATCACA | 23092 |
| rs116385721 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143958 | TCTTGTTTTCTGTGA[C/T]TGATACAAAGACAGA | 23092 |
| rs116389069 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072504 | TATGGTACCAACCTA[C/T]GTGTCCAGCAGCAGA | 23092 |
| rs116397065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865686 | CCAACAAAGTTCTGG[G/T]CCAGCTCCTTAGTAA | 23092 |
| rs116400434 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099960 | AACATAGCTGATGCA[A/G]TAAATATCAGACTAA | 23092 |
| rs116404063 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811997 | TCACCTCCTGAAATA[A/T]GCTTACTCATCACCT | 23092 |
| rs116406456 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780207 | TTGTTAGATTGCATT[G/T]TATTCTATTGTATGA | 23092 |
| rs116413682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035511 | CGAAGGCACAAGAAT[A/G]ACACAATGGACTTTG | 23092 |
| rs116415685 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910748 | CATCTCAAAAAAAGA[A/G]AAAAAGAAGAAATAG | 23092 |
| rs116419617 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017606 | TGTTCTTGATAAATG[A/G]TGTGTGTTAATAAAT | 23092 |
| rs116420047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148206 | CTAAGTGAAAATACA[C/T]TGAGGTTCAGCCACA | 23092 |
| rs116426460 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144673 | TTGGCCTCTGAAGGC[A/C/G]ATGGGATTACAGGCA | 23092 |
| rs116426566 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916367 | TTGTGAGTTGATTAC[C/T]GTACATCAACGTATT | 23092 |
| rs116434891 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201255 | GGGGCCTGGCAGGAC[C/G]CCAGGAATATTTAGG | 23092 |
| rs116435599 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816229 | CCCATGAGGGTAGGA[A/G]CCATGTCTTTTTTTG | 23092 |
| rs116442354 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926147 | GTGGTCCCAGGATCC[C/T]GAATGTGTTGCTAAA | 23092 |
| rs116442908 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939424 | CTCCATTTTAAAGAT[A/G]TCTTCTGTTTTCGTC | 23092 |
| rs116461606 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088765 | TATCCCTGACATATG[C/T]GATCCCTGCCGCTGT | 23092 |
| rs116467820 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177937 | TTTCTAAATGAGGGA[C/T]ACTGAGGCTCAGAGG | 23092 |
| rs116470042 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210562 | AGACACATTCCCTCC[A/G]TATTTCCCTTTTCTT | 23092 |
| rs116473366 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111651 | AAGAAAAGGAGAGAT[A/G]GGAGACACTGTCTTA | 23092 |
| rs116478745 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797286 | AAGGACTGATTTTCA[A/G]CATCATAGGAAAGCA | 23092 |
| rs116485064 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065254 | TCATGAAATGCCTCT[C/T]TTTTTGGCTGAGTGG | 23092 |
| rs116497563 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776445 | GATCTACTACTTTCT[A/G]TCTCTATAGATTTCT | 23092 |
| rs116500885 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854421 | TCTCCAGTAGGTTGT[A/G]GGTTTGGGGAACGTA | 23092 |
| rs116527516 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143695 | CTTATAACCATTCAC[A/G]GAGCCTTAGTGTCAG | 23092 |
| rs116535692 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928387 | GTTGCCTAGAGTAGC[A/G]TTGTAAGCCCTCATA | 23092 |
| rs116538943 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018691 | TTATTCAGGTTTTTT[A/G]TGTAGCTGTTTTTGT | 23092 |
| rs116546640 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090826 | TTACATTGGGGAGCA[A/C]GACTCCTGGTTGATA | 23092 |
| rs116560626 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117637 | GAATTATGCTGGGTA[A/G]CCTCAAGCTTATTTA | 23092 |
| rs116572939 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809390 | AGAAGAAGGGGTCAG[A/G]TCAGCTGGTGCAATT | 23092 |
| rs116576247 | snp | C/T | 0.0341408 | 0.126114 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229473 | CACTGAGTCTTCGCA[C/T]TCATCATGTCCCTTC | 23092 |
| rs116594265 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856663 | TGAACATGTACAGAC[G/T]TTTTTTTCTTTTTTC | 23092 |
| rs116611449 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912845 | TGGAGAAGTGATGAC[A/C]AACCCAAGATCATAG | 23092 |
| rs116612571 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146227 | GGTGGATGCTGGTAC[C/T]ATTTAGCTAAATTAT | 23092 |
| rs116615112 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963495 | AGCATTTTCTTTTCT[C/T]CACAACCTTACCAGC | 23092 |
| rs116645830 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119702 | ATCCTCTTTCTAACT[G/T]GGCTGTGCCACAGTT | 23092 |
| rs116648438 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042218 | ATAGCTTATGACTCC[C/T]TCCGTTCTCTTTTGG | 23092 |
| rs116649477 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012970 | ATTTTTTTCTTTTCT[A/C]AAGTAGAGGTTTCAT | 23092 |
| rs116660451 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007110 | GGAGACAGGTGAATC[G/T]CTTGAACCCAGGAGG | 23092 |
| rs116678487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884797 | CCTGCATGTGATATT[A/G]AGTGTCAAGAGATAT | 23092 |
| rs116691047 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210980 | GGAAGCCAAAGAACC[A/G]ATGATGCCTGGTGGA | 23092 |
| rs116699251 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039896 | TATTTTAACTTCTAC[A/G]AAAGTCTTCATTGAG | 23092 |
| rs116703403 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040445 | TATACTGGCCTTGAT[A/G]GAGTATAATCTCGTG | 23092 |
| rs116703718 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224810 | GGAAGACTCCAGGAG[A/G]GGTATAGATTGTGCC | 23092 |
| rs116708266 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167655 | TAGTATGGGGGCAAG[C/T]GCATGACTAAGCCAG | 23092 |
| rs116708468 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200784 | TCAGCTTACTCCTCC[A/G]GTTACAGAACCTCTC | 23092 |
| rs116711193 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774024 | TCTCAAAGGATGTTC[A/G]ATGCCAACCTGCTTT | 23092 |
| rs116712763 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837177 | GTTTGGAGGCAAGAA[A/G]GCCTGGGATTAGGTT | 23092 |
| rs116713315 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101111 | AAACAAACAAACAAA[C/G]AAAAAACCAAAGAGT | 23092 |
| rs116714376 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769386 | AGACACCCTGTGGGA[C/T]CCAGCCTGACAAGTG | 23092 |
| rs116714550 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813333 | GAAAGGCAATACCAG[A/G]TCAGTCTCCATTGAC | 23092 |
| rs116720714 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026872 | TCCAGGCAAAGGATG[A/G]TGGCAGCTTGGATCA | 23092 |
| rs116735057 | snp | G/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911914 | GACAATAGGTATAAG[G/T]CCTGTGAATATAAAC | 23092 |
| rs116761063 | snp | G/T | 0.0547245 | 0.156101 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122568 | TGCGATTCTAGAATT[G/T]GGCAACACCTCATTC | 23092 |
| rs116770437 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093925 | TTCATGGGGATTACT[C/T]GCCTCTTTTTGAGGT | 23092 |
| rs116770933 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909143 | CCTCCTTCCCATTCT[A/G]TTGTCTCCCTCTGGA | 23092 |
| rs116770940 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052631 | GACCCTTTCCTCTCT[C/T]ATAACCCAGTATGTG | 23092 |
| rs116783653 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860852 | TTACTGGTACTTAGT[A/C]TTAGATGTTCTGAAG | 23092 |
| rs116787713 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006669 | ACCACTCAGACCATG[G/T]TGATGAGAGTCACAT | 23092 |
| rs116795029 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884944 | TAGGTACCCCCACTG[A/C]TGCTGCTCCCCAGCC | 23092 |
| rs116797388 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139642 | CAACTACACAGAGAG[C/T]GATATGTGTTGAATG | 23092 |
| rs116800043 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105094 | AAAATAGGCCTAATC[A/G]GCTGGGTGTGGTGGC | 23092 |
| rs116805162 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030258 | TGTTTTCCAGGGGCT[C/G]TCTTGACCCTCAGGC | 23092 |
| rs116810738 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855412 | CCACTTAAGGAGGCT[C/T]TCGTATCTTTTGCAC | 23092 |
| rs116812297 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905156 | GTTTTAGGTCTACTT[A/G]AAAATATAAATTTTT | 23092 |
| rs116812868 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939162 | CACTGCCTAAAAAAG[A/G]CTGGTAATTGGTTGA | 23092 |
| rs116818604 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055253 | AAGTCTCTGTGCAGA[G/T]TTTTTGAAGATGGAA | 23092 |
| rs116819028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143795 | TATGGCCAGACAGCA[C/T]GTCCCTGCCCTCGGG | 23092 |
| rs116887043 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056161 | GAGTCAGTATCCCAA[A/T]ATAAATATTACCTAA | 23092 |
| rs116911710 | snp | C/T | 0.011527 | 0.0750375 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166010 | CGTAATTATGGTCAT[C/T]GTTGCTCTTTTAACA | 23092 |
| rs116927643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114363 | TCACCGAGTCCAGGT[A/G]GTATTCAGGCAACAC | 23092 |
| rs116931274 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122148 | AATGTTAAGCCAGAT[A/G]GTATCAGTTTTCTCC | 23092 |
| rs116940773 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128709 | TCAACTGTTGTAGGT[C/G]TACTTTCCTAATGCG | 23092 |
| rs116942464 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093278 | GCTACAGGTTGAATG[C/T]ATTTGGGCCATCTGC | 23092 |
| rs116959266 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182007 | CTTATTCTTGTCCCC[A/G]TACAAAGCACATCCA | 23092 |
| rs116960202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993871 | AGGCTAGGACTCCTT[A/T]TGTTGCCCAGATCAG | 23092 |
| rs116969290 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199502 | CAAGGAAGAAGAATT[C/G]AATGAAATGGGATTA | 23092 |
| rs116975327 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997554 | GCTGGGACTACAGGT[C/G]CATGCCACCCATGCC | 23092 |
| rs117000519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801379 | CTTGTATGTACTGTC[A/G]TTCAGTCATCAGAAC | 23092 |
| rs117003583 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812332 | AGTCATGGCTCACTG[C/T]ATCCTTAAACTTCTA | 23092 |
| rs117035912 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221609 | GCCTCGACCTGCTGA[A/G]CCCAAGCGATCCTCC | 23092 |
| rs117041546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208153 | TGCTTTTGTGACTTC[C/T]GCACTTAAGTTTTTT | 23092 |
| rs117084726 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009843 | CTTAGCTTCAGTTGG[A/G]TTGTTGAAGGTGCAT | 23092 |
| rs117103394 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870300 | GCTGCTCCATATCCA[A/G]GGTGAAAATCTACAT | 23092 |
| rs117104029 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837605 | ACTTTGTGCAGCTGC[A/G]GAGCTTAAGGGTGAG | 23092 |
| rs117110005 | snp | A/C | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815775 | CTAGCCTTCCTGGTC[A/C]ATCTGTGCTACTGCT | 23092 |
| rs117115522 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142641 | TTAGTGTGGCTTGGC[A/G]TGTCACTATTATCAG | 23092 |
| rs117142668 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915327 | GAGATTTCAGTCATG[A/G]TTCAGTTGAGGGGGC | 23092 |
| rs117146924 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951049 | TCCCTTTCCCTTCCC[C/G]TTCCCCTTCCCCCTC | 23092 |
| rs117171988 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030510 | CCCATTCTTGGGCTT[C/T]GCTGCTAGGTGGCAT | 23092 |
| rs117190482 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833752 | GAGATGTGGCCACTA[A/C]CCCTACAGAGTCTGT | 23092 |
| rs117219572 | snp | C/G/T | 0.0165278 | 0.0893908 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004499 | AGCCCAGGAATGCCC[C/G/T]GGATGCCTTCTAGAC | 23092 |
| rs117220888 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171247 | CATTTTACAGATGGG[G/T]AAACTGGGTTTCAGG | 23092 |
| rs117221124 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032821 | AGTGGAAATCAAGCT[C/T]TTTGTGTGTGTGCAT | 23092 |
| rs117223977 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149918 | GGATATCATTATGAC[C/G]AGAGAGAAATCATAG | 23092 |
| rs117297545 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846082 | CATGTGTGAAAGCCA[C/T]GCATTAGTTTCAAGG | 23092 |
| rs117308761 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985377 | TACAGTGTTTATAAA[A/G]TCTACAGTATTGTGC | 23092 |
| rs117321021 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146114 | GATGTTTAAGTGAAT[A/T]AATTTTCAGAAATAT | 23092 |
| rs117331853 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916371 | GAGTTGATTACCGTA[C/T]ATCAACGTATTTTAC | 23092 |
| rs117342265 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913819 | ACTCGTGAAATCACA[A/G]TTTTTTGGAGAGAGA | 23092 |
| rs117365138 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142985 | TTCGCTCTGTCTGGT[A/G]ACTCCCTTTTCTCCT | 23092 |
| rs117377093 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040004 | TTGCAGTGTGTGTAT[A/G]TGCATACGTATTTAT | 23092 |
| rs117393109 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193382 | CCTCTTGAATAGCTG[C/T]GATCACAGGTATACA | 23092 |
| rs117419993 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064621 | TTGCACAGAGCACAA[C/T]GACATATTTTAAAGC | 23092 |
| rs117467591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086906 | AAAGTTTTGGATCCT[C/T]CCCGCCTACCCCCTA | 23092 |
| rs117490166 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041385 | CATTCTTACACCTCC[A/G]TATTTTCATTTTTTG | 23092 |
| rs117527772 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102892 | CTATGAAATAGACCA[A/G]GGAAGAGGCAGCACA | 23092 |
| rs117539789 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892384 | AATCCCAGCTCTGCC[A/G]TATACTAGCTGTGTC | 23092 |
| rs117553552 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196252 | CTCCCCCATCACAGT[A/C]CTCTTCTTCCCCACA | 23092 |
| rs117576564 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031936 | TAACCTGCCTCCAGC[C/T]TCCCGGGGTTCATAT | 23092 |
| rs117621687 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043056 | TGTGTACCACTTACT[C/T]AGTCTCCTCTAAAGG | 23092 |
| rs117634534 | snp | A/G | 0.0327778 | 0.123752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818543 | TTAAAAAAGCAAGGT[A/G]GTGAGATGGCTCAGA | 23092 |
| rs117660855 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883629 | ATGGCTTCTGGCTCC[A/G]AGTGTCCTGCCCCAG | 23092 |
| rs117730609 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847081 | TTGCTCTCGGTGCAC[C/T]TTGGGCAAATCACTG | 23092 |
| rs117752823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995962 | GTTGTGTTCTCACAA[C/T]TCCCACTCCCATAAG | 23092 |
| rs117758129 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146935 | AGTCAAAAGAAGATG[C/T]AATTTATGGTGCCAT | 23092 |
| rs117762306 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094318 | ACAGTATGTGAGGAT[C/T]CTTTAAGCTAGGTTG | 23092 |
| rs117768878 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810834 | AGTAAGTAACCATAA[A/G]CGTTGATATGTAAAC | 23092 |
| rs117770276 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846252 | TCTGGTATTATCTCA[C/T]GGGCCTGAGACCTTT | 23092 |
| rs117782528 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923739 | TGTGGTTGGTGATAC[C/T]TACTTTTTAGACTAT | 23092 |
| rs117785724 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007292 | TCTGCCACAGAGTCT[C/T]TGGCAACCCTGGCCA | 23092 |
| rs117800216 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083911 | CAAAGGTTGAGTTTC[A/G]AGTCATTATATTACG | 23092 |
| rs117819807 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180482 | ATCAGCAACATATCT[A/G]TGTTGGTGCATTTTG | 23092 |
| rs117823110 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127489 | GAGCTGTTAATTCTC[A/G]GAAATCCCCAAAGAT | 23092 |
| rs117827044 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865149 | AAATACAGTACCTCA[A/G]TTCTCTGTGCCAGGG | 23092 |
| rs117842955 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859796 | TGTCCTAGGTTACCA[G/T]GATCAGTGTCAGTGG | 23092 |
| rs117844324 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000408 | TTGATAAAACTATGG[C/T]ATATTCAAACATTAA | 23092 |
| rs117848107 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054690 | GTCAAACCAATCGTA[A/C]ATCATCCATAGTTGA | 23092 |
| rs117858431 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098511 | AATCTACCCTCAAAA[A/G]CTAGTGTAATTTTAA | 23092 |
| rs117868161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187761 | GCAGGACTGTTGGGA[C/T]GAGTCAGTGACAGGG | 23092 |
| rs117883707 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211343 | CTGCCATCCAAATCT[A/G]ACTAGGTGTCCTGTA | 23092 |
| rs117906723 | snp | C/G | 0.0644444 | 0.167538 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147050 | AATTTCGAGTCACCT[C/G]TTCCCCCTTGACTCT | 23092 |
| rs117922592 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928943 | CCATATTATCCTCCT[C/T]CTTTTTTTATTTTGA | 23092 |
| rs117941844 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791203 | CCTGCCTCAGCCTTT[A/T]GTCTTGGATAAACCA | 23092 |
| rs117963758 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204520 | CAAGAGCAAAACTCC[A/G]TCTCCAGAAGAAAAA | 23092 |
| rs118002193 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206837 | GGAAGCTGAAGGCTC[C/G]CTATAAGCTAGCCCT | 23092 |
| rs118022167 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033871 | CACCTGACTATTGAA[C/T]CGTAGTTATAAACAT | 23092 |
| rs118042096 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803510 | TTCACGAAAGGTCCC[A/G]TCATCTATTAAAACA | 23092 |
| rs118045963 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812912 | CTGCATGTTAATTCT[A/G]TATAATTTCTTTTTC | 23092 |
| rs118104082 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823424 | TCTCTTCTTCCCTGC[A/G]GAAATAAAGCCACAG | 23092 |
| rs118113359 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085137 | AATTGTGGTCCCGGC[C/T]CCGGAAACTCTTGAT | 23092 |
| rs118125147 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195130 | CTTTTCATCAAAGTT[C/G]ATCTCTCTTTCTCTC | 23092 |
| rs118134771 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876701 | AGGATCGCTTGTGCC[A/T]GGGAGGTCAAGGCTG | 23092 |
| rs118140154 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827893 | GATTCTCCTGGCATC[C/T]GGGAAGTGTAGATAC | 23092 |
| rs118174779 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197968 | TGTCTAGTCCATATC[C/T]GTACATCCAGTTCCC | 23092 |
| rs118184223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831215 | GATGGAGCCAGATCC[C/T]AATACTCTGTGCTCA | 23092 |
| rs121918546 | snp | A/C/G | 2.89901e-05 | 0.00380713 | ARHGAP26 | 5 | allele_origin=G(somatic)/A(germline) | 5:143041855 | GAATTGTGGGTGTCA[A/C/G]CTCCAGAGTGCAGAA | 23092 |
| rs137862790 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072446 | CATTGAAGAGACATC[G/T]GCACACTAATGTTTC | 23092 |
| rs137865055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023788 | AGTGCAGCATCCCCT[C/T]CAGCTTTCTCTCCAG | 23092 |
| rs137865321 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996209 | AAATGAAAATAGGTT[C/T]GTGGCTGGGTGCAGT | 23092 |
| rs137874641 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920916 | ACAGGGGACGATGGC[A/G]TGACTGGAATACGCT | 23092 |
| rs137886514 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955794 | GATGTTAGTCTTGTT[A/G]TGGCCTCTTTGGCCA | 23092 |
| rs137889056 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852357 | GGAATTGGCCCTCCT[C/T]ACAGGCATTGCTGAG | 23092 |
| rs137889264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881728 | ACAAACAAGCAAACA[A/G]CAGATCCACTTCTAG | 23092 |
| rs137889973 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892274 | AAGAATCTGTCTCCC[A/G]TGGAACCCAGGTTGT | 23092 |
| rs137897465 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823324 | AACATGATCAGTATA[C/T]GCAGATTACAAATGT | 23092 |
| rs137899464 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778358 | ATCAAAGAGTATAGA[C/T]GTATACAGTGTAAAA | 23092 |
| rs137919940 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174033 | AGCAGGAAGGGTGAC[A/T]TCTGTTTCTTCCAAT | 23092 |
| rs137924037 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107671 | TGACTCTTGCTGAGA[A/G]TGTGAATGTTGGGTG | 23092 |
| rs137924876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810980 | GTCAGATGAATAAAT[C/G]TACCCGCTTCCAGTC | 23092 |
| rs137935050 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783272 | ATGTCAGCCAGTGTG[A/G]CTCCACGCCTGGGAT | 23092 |
| rs137938690 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177832 | CTTGTTCACTATTGT[C/T]TCCCCAGCACTTGAG | 23092 |
| rs137948920 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112537 | TTCAGTGGTGGTGTA[C/T]AGTCACCAACACCAT | 23092 |
| rs137949532 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143068706 | TTCTCAATCCCATAT[A/C]CCCTTTTAGGTACTA | 23092 |
| rs137952267 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165661 | CTTCTAATGTACCCA[C/T]CACCCAATAATGAAC | 23092 |
| rs137962553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793065 | TTCTGCCAGCTTTGT[A/G]GAACAGCATGAATCC | 23092 |
| rs137964086 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817794 | TGGTGGAGAGTGGTT[G/T]TATCAGCATTATTTT | 23092 |
| rs137980552 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082667 | CTTGAGCCTATTTTG[C/T]TCTCACTATACTGTA | 23092 |
| rs137984477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137488 | TGCCACAGAGCAGAT[A/G]CCTGGTTGGAGGGAT | 23092 |
| rs137986521 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201645 | AGTCTTGGGCCATAA[C/T]AACCATCCCTGTGCG | 23092 |
| rs137997602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038099 | AGAAAAGCTATTAAC[C/T]ATCTTTCCACTGGAT | 23092 |
| rs137999982 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965592 | AGGTTATGATTATAG[A/G]GCGAGGATTATTATA | 23092 |
| rs138006748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003769 | TTAAATTCTGTTAAT[A/G]CTCTCATAAGTATTA | 23092 |
| rs138011735 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095102 | GGGTTCTAAGATAAT[A/G]TATTCTTACATATAT | 23092 |
| rs138011882 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847099 | GGGCAAATCACTGTG[A/C]CTCTCTCACCTTCTG | 23092 |
| rs138014820 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992085 | TTTGAATATTCCCTA[C/T]GGTTATTGAATTCTT | 23092 |
| rs138018183 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217794 | GGCCGCCTGACACAT[C/T]TTGTCACTGGCTTCC | 23092 |
| rs138018413 | snp | A/G | 0.00188445 | 0.0306378 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142770922 | CGCTCAAGAGTGAGT[A/G]TCCCGAGCCCCTCGG | 23092 |
| rs138023791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915548 | TATTTTTAGTGGAGA[C/T]GGAATTTCACCGTGT | 23092 |
| rs138042282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877616 | GTAGTATGGCTGGGC[A/G]AAGGACTTGGGGGTC | 23092 |
| rs138046358 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806581 | TTTTGGGAAGGCATT[A/G]GTTAACATCTTTGTA | 23092 |
| rs138048108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187108 | CTTTAATTATCACCA[A/G]TCCTATGAGGTGTAA | 23092 |
| rs138058740 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889992 | AATACAAAATTGGCC[C/G]GGCATGGTGGTGCAT | 23092 |
| rs138059494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220808 | GTGTACCCAAAGTTG[A/G]CTGACACTGATCTTC | 23092 |
| rs138059667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777058 | TGTTGGCCATTGGTG[C/T]GTCATCTTTGCTGAA | 23092 |
| rs138072692 | snp | A/G/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018477 | TTATGAGTGTGTCTT[A/G/T]CACATTTAAGTTTCT | 23092 |
| rs138073070 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067943 | CCAAAGCAGGCAGAT[C/T]ACTTGAGGCCGGGAG | 23092 |
| rs138078958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945593 | GGAAGATGATATTTT[A/G]GCAAGTCAAGAATTT | 23092 |
| rs138079878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162255 | TTCTTCTGGAGGAGA[A/G]ACAGACACTCTACTC | 23092 |
| rs138093609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196831 | AATGTGCCGTTGGGC[C/G]ACTCAAGGTTTTTGC | 23092 |
| rs138117585 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902800 | ACAAAGCATGGCTTC[C/G]CCTTAGGCCAGGTTT | 23092 |
| rs138137101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158436 | GCCAACTGGAAACTA[C/T]GCTGATTAGGCTAGA | 23092 |
| rs138157096 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905136 | TGAGAAGATCCCTGC[A/C]AAAGGTTTTAGGTCT | 23092 |
| rs138165221 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142959838 | AGGGAAACCTCAGGG[G/T]AGCTATTTTTAGAAT | 23092 |
| rs138169840 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884787 | AGCTTAAAGACCTGC[A/G]TGTGATATTAAGTGT | 23092 |
| rs138170028 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844812 | GTGAGCCGAGATCAC[A/G]CCACTGCACTACAGC | 23092 |
| rs138177350 | snp | A/G | 0.0178098 | 0.0926698 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228094 | TGGAGCAGTCCTGGA[A/G]AGGTTAAGACATTCT | 23092 |
| rs138179488 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051454 | AGCAGTGGTCAAGGG[A/G]CATGGTGGAGAGAAG | 23092 |
| rs138182141 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982442 | GGGTGTCTTGTAGTG[A/G]GAGGGTGTCTTGTCC | 23092 |
| rs138191124 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169221 | ACAGACAGTTCTATT[C/G]AAGACCCTGTATGTC | 23092 |
| rs138201954 | snp | C/G | 8.25389e-05 | 0.0064236 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143134003 | ATGCCTCTCACCAAT[C/G]CCCAGCTGCACCTGT | 23092 |
| rs138206830 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015076 | AGTTTTGTATGAAAT[A/G]TTAAATAATTTGGAA | 23092 |
| rs138216148 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133233 | TCCAAAAAAAAAGCT[C/T]ATAAATAAATAAAAC | 23092 |
| rs138216234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938437 | ACTTTTCATATTAAA[C/T]TGGACACGGAAACCT | 23092 |
| rs138217810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063168 | TTCTCCAGTCCTATC[A/G]GGCTTTTCCCTCACT | 23092 |
| rs138261454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856649 | TATTGCATCAGTACT[C/G]AACATGTACAGACTT | 23092 |
| rs138269761 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975448 | GTCTGTCTATTTTTG[A/T]TAAAAGATATTCTGT | 23092 |
| rs138275948 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876994 | TGCTGGTGCCTAAGA[A/G]AGGGAAATGATTCTT | 23092 |
| rs138281058 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769737 | GGAAAATAACAGGCG[C/G]CTGAAATTCTAGTAA | 23092 |
| rs138296560 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091583 | TGTATGACTTTTATA[C/T]CAGATAAACTAAATT | 23092 |
| rs138300898 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158203 | TCAATGTTTACTTTT[A/G]TTTATTTGTTTGATC | 23092 |
| rs138304171 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797851 | TGTGCATCCAGATTG[C/T]CTGGGGACCTTGTTA | 23092 |
| rs138308169 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178972 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCTTCA | 23092 |
| rs138323262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162064 | ACTTTGACTTGCGCA[A/G]TGCTGCTGGAAGGTT | 23092 |
| rs138326683 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009236 | TTCTGACTCAGGGCA[A/G]GTTCTTCCTTCCGGT | 23092 |
| rs138327920 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143246 | CGGGCCTGCCAAGAC[A/G]TGTGAATTTGGCTTG | 23092 |
| rs138333559 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094714 | TGTCATTCCCCTATT[A/G]GCTAGGGTTAGACAG | 23092 |
| rs138347768 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978434 | TGGCTGGTGCTGCTC[C/T]CATCATTGACATAAC | 23092 |
| rs138348103 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971754 | AAGAGGCCATACCCT[C/T]AACTTTTTCAATTTA | 23092 |
| rs138350432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893717 | TACATTCCCACCATC[A/C]GTTCCCTTTTCTCCC | 23092 |
| rs138350751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803732 | TCTGGTGGCATCTGG[A/G]GATGTGTTCTTGGGC | 23092 |
| rs138356541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064188 | CAGGGTGTGCCTTCT[C/T]CAGTTTGCCTTAGTT | 23092 |
| rs138357050 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874540 | GGCCATTGCACGTAA[-/T]GCTTATTGCTTTTAT | 23092 |
| rs138367804 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885063 | CTTGGCTTTGCCACC[A/G]TTAGATATTCGTATT | 23092 |
| rs138395837 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772160 | CAGGTGCCTGAGATG[A/T]CATTTTGTCAGCTTG | 23092 |
| rs138404707 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830700 | TCCCAAGCAGTTCTT[A/G]TGGGAGAGACAGACA | 23092 |
| rs138406499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204654 | CGTGTAGTTCTGGCC[A/G]AAAACCACTTAGATA | 23092 |
| rs138421320 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829293 | TTATTAACAGTGCCC[C/T]CTTTCTCGAAACCGT | 23092 |
| rs138431578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115490 | AGAAGTCTTTGAAAC[A/G]TAAGTGGAGAAGATG | 23092 |
| rs138438275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170475 | GCTGGAAAATTCCAC[C/T]TCAGTTTGATCTTCC | 23092 |
| rs138439268 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872504 | TGCACATGGAATTAA[A/G]TTAAGCACATTTGTC | 23092 |
| rs138439662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207135 | TGGCCTCCCATGACC[C/T]CCTGTGCTCCCATTG | 23092 |
| rs138443467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045324 | AGAGCTGCAAGATGA[C/T]CACAGTGTAACATCT | 23092 |
| rs138453302 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824591 | GGCAGCATGGAGCTC[A/G]GCAGGATTAAAAGGA | 23092 |
| rs138453659 | snp | C/T | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868970 | GTCCGAGGCACTCTT[C/T]GTGCATTGTGACATG | 23092 |
| rs138456934 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929769 | GCCATGAAGTTGATG[G/T]AATATATGTGAGCCC | 23092 |
| rs138471770 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169805 | ACCTTTCTTATGGGG[A/T]CTTCGTGAAGGATTT | 23092 |
| rs138484319 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932778 | TGTGCAAGGAAGAAG[G/T]AGGCCATGGGCTCCA | 23092 |
| rs138506688 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032539 | GGACAGCCGCCTCCA[A/T]CTGGCGAGCCACTCA | 23092 |
| rs138514825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960210 | GTTTACATACTTCTG[C/T]CCTTCCCCTGATGAC | 23092 |
| rs138520266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214851 | AGAACTGCATGTGGG[C/T]GTCTGAGTCTGCATT | 23092 |
| rs138532001 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153926 | GGAATTCAAAGGATA[A/G]ACAAGGCCTGCGTCC | 23092 |
| rs138532527 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916203 | AGATACAAATACATG[G/T]TGAAGTGTGAAGTAT | 23092 |
| rs138534031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848058 | AATCCAATTGAATGG[C/T]AGTGTCTGAAGGTGG | 23092 |
| rs138549214 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000131 | GATTGGCAAGTGCTG[G/T]TGAGGATGTGAAGCA | 23092 |
| rs138558649 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058456 | CTTGACCCTTTCACA[A/G]ATGGCATTGCTGACT | 23092 |
| rs138560463 | snp | C/T | 0.000384235 | 0.0138553 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143041823 | TTCCTCAGGGATCAA[C/T]GAGCAAGGGCTGTAT | 23092 |
| rs138564541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115637 | TCATCAGCACTACCT[C/T]GACAGCCACCATGAC | 23092 |
| rs138574447 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073650 | GCCTTCAGTTTCTTC[A/G]TCTACAAAATGAAAG | 23092 |
| rs138576476 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142946 | CTATTTTTTTTAATA[C/T]AAATCTCCTTGTCTT | 23092 |
| rs138589979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942744 | CTATTTGATTAATGT[C/G]TGTCTGCCTGCTGGA | 23092 |
| rs138603045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079318 | TCTCCTTTGGAGACT[A/G]CTAGAGCAGAAACCT | 23092 |
| rs138604179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145565 | TTATGTAATCTTAGC[A/G]TTGTTTTTCTTTCTG | 23092 |
| rs138604362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028141 | TTAACCTGACTGAGC[A/G]TAGGTTTCCTATCTA | 23092 |
| rs138608058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215564 | TGCCACTATATAATT[C/T]CAGAATATTTTCATC | 23092 |
| rs138608375 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951022 | CTTTCCCTTTCCCTT[C/T]CTCTTTCCCTTTCCC | 23092 |
| rs138611806 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128607 | CTTGCCTGGCTTCCA[C/T]TGTGAAGGTGCTGGG | 23092 |
| rs138617448 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956700 | ATTTTTACACTGCTG[A/G]TAAAGACATAGTTGA | 23092 |
| rs138620429 | snp | C/T | 8.29029e-05 | 0.00643775 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142873412 | TAGATTTGTCTTCAG[C/T]GAAGCGGAAGTTTGC | 23092 |
| rs138644599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859644 | CATTCTTCCAAGAAC[A/G]GTGGAAATGTTGCAC | 23092 |
| rs138644995 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164988 | TATGCTGCCACAGCC[C/G]TATGCTTTGCTTTAC | 23092 |
| rs138646692 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813782 | CTCTATTTCCAAATA[C/G]AGTCCCATTCTGAGG | 23092 |
| rs138646848 | snp | A/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228871 | GTGTCACCAAATATA[A/T]CTATAAAGAAAACAA | 23092 |
| rs138650282 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224294 | CACTGTCCCCGCTTC[A/G]GCCTGAAGGAAAGAG | 23092 |
| rs138652030 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881514 | CCTCATGCATATTCT[A/G/T]TTCTCCTATTCATTA | 23092 |
| rs138660667 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810168 | GATACTTTAGTTTTG[A/T]CTGGGAGGGGCAGGG | 23092 |
| rs138666352 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995799 | TGGATGAAGAAAATA[C/T]GGCACATATACACCA | 23092 |
| rs138682779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817209 | CAGGCAGAGAAGCAG[A/T]TGGGAGGGGAGGGGG | 23092 |
| rs138685953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197388 | ATTCTCATAAACCTC[C/T]GGTATTTCCAGCATT | 23092 |
| rs138695046 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133849 | ACTGCCAGTGGTCTT[C/T]TCGGATCTTTTCTTG | 23092 |
| rs138696196 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225672 | CTCTGATTTGAAATC[A/G]GGAGAAACAGAGCTG | 23092 |
| rs138699511 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997032 | GACTGTTGAAACTAC[-/T]GAACTCTATTGTAGC | 23092 |
| rs138719363 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193874 | ATACATATAAAAAAC[A/G]TAGTATATACATAGT | 23092 |
| rs138722907 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041480 | TTAATTTTAAAAATT[G/T]GTTAAATATGACATA | 23092 |
| rs138725861 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806736 | CACTACTTAGACATC[C/T]AACTCTGTGTTAATA | 23092 |
| rs138763700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190659 | AAAAGAAAAAAATTA[A/G]CAAATTGAACTTGAC | 23092 |
| rs138780896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920492 | AACCATGTGAAAAAT[A/G]ATAAAACTTTTTCTG | 23092 |
| rs138791101 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090536 | GGAAGGTGCAGGTGG[C/T]GGGGGATCAAAGAAA | 23092 |
| rs138793406 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025924 | ACTTTACTCTATGTC[A/T]CTTTCAGCTTATTTT | 23092 |
| rs138795557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906049 | GAACAACACAGTCCA[A/G]TTCCTTTATACAGTT | 23092 |
| rs138795795 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014793 | ATGTTTGGGCTGATT[A/T]TCTCCTTGGTGTATA | 23092 |
| rs138798405 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051982 | GGATGGGGAGGGAAA[A/G]AGGTCATGCAAAGCA | 23092 |
| rs138800587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982613 | ACCCAGTGTGAGCCA[A/G]TTCCAGCCTCGCTAT | 23092 |
| rs138815313 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977188 | GAAAGAACAGATGTT[C/T]CTCATAATGAGCAAT | 23092 |
| rs138816437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897515 | CTCAGTGTTAGACAT[A/G]CACATTCTCAGGCTT | 23092 |
| rs138834264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990269 | GAAGCTTGTGATTGC[A/G]TCATGTAGTTCTTGT | 23092 |
| rs138835559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911371 | CCAAGCCTATGTGGA[C/T]CCTGACCCCAGGGCC | 23092 |
| rs138870105 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949202 | GAGAGAGAGAGAGAG[-/A]GAGAGAGAGAGAGAG | 23092 |
| rs138884501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128385 | TTACCCAAGCTGTCT[A/G]TATATACCCTCAGTT | 23092 |
| rs138891270 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201172 | AGTTGAATCCAAACC[A/G]GACCAGCAAATGTTC | 23092 |
| rs138892627 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009404 | ACCGTGGGAGTTCCT[C/G]TCTGGACTCTGCCCA | 23092 |
| rs138915071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095918 | ATACAAAAATCAGTC[C/T]TAGCATATGCATATA | 23092 |
| rs138926742 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146745 | ACATTGGTGGCTAAA[C/T]AGTAGATCTTCTCTG | 23092 |
| rs138930924 | snp | A/C/G | 0.000164731 | 0.00907422 | intron-variant, missense, synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207346 | TTTTCTGTTGCTGCC[A/C/G]TTGTTCTCTCATTGG | 23092 |
| rs138938983 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046072 | CCGGGAGGCGGAGGT[G/T]GCAGTGAGCCAGGAC | 23092 |
| rs138948443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864867 | TGGGAAGTGAGAGAC[C/T]GGGATTTAAGCTGAT | 23092 |
| rs138953318 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098928 | GTATAGAATAAACAC[A/G]TCAAAGGTCTATGAG | 23092 |
| rs138958633 | snp | C/T | 0.126219 | 0.217206 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793629 | GTCTCACTCTGTCAC[C/T]CAAGCTGGAGTGCAG | 23092 |
| rs138958848 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022817 | CCCTAGCCTGCCTCA[C/T]TGCCAGGGTCATTTT | 23092 |
| rs138966150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933609 | ATTGCTCCAGTCATT[C/G]CCATTTTCCAGCCAG | 23092 |
| rs138978030 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796773 | ATTTTTTCTAATGGA[C/T]AATGGGTTTCCCAGC | 23092 |
| rs138986844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178443 | TTGCAAGAAACATAG[A/G]AAGATGGGAGACTGC | 23092 |
| rs138992221 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789643 | AATTGTTTGTGTTAA[C/G]GACTGATCTCCATTC | 23092 |
| rs139023168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798998 | CCTGGGCATGGAAAC[A/T]GCCCTGTTTAGGTGA | 23092 |
| rs139025211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843498 | CTCCGTGCCAGACAT[G/T]CCAGGCAAACCCACG | 23092 |
| rs139034002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982105 | GCCCTGTGACCAAAT[A/G]TTTAGCAGGCTGTTC | 23092 |
| rs139034376 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221487 | AGCAGGGGGTAAGGA[C/T]TTGAAGGAAAGTAAG | 23092 |
| rs139040167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901561 | CTGGTCTTTGGTTTC[A/T]GAGGAAATGATGTTC | 23092 |
| rs139058232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191271 | TGTTTTTATTATTCT[A/G]TAGGTAGTGTAGACA | 23092 |
| rs139060525 | snp | A/C/T | 0.0075629 | 0.0610735 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952475 | CAACATCCTATGTAC[A/C/T]GTAGTGTGTCTGCAA | 23092 |
| rs139063905 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802590 | ATCGACGATGTTAAG[C/T]GGGGATTCCATGTAA | 23092 |
| rs139064400 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125464 | GGTCAGATAGAGTGC[A/G]CTAACGACATGCTTA | 23092 |
| rs139065675 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217089 | TGTGTAGTTGTCAGA[A/T]TAAATGATCAAACCA | 23092 |
| rs139066564 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878744 | ATAGCCAAATGCTAC[A/G]GCCCTGAGGTGGGAC | 23092 |
| rs139066603 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837056 | TTTGGAAACCAAAAC[A/G]GTTTTTGTCTAAAAT | 23092 |
| rs139067532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182605 | AACCCTGTCATTAAC[A/G]TGGAAGATGCACAAG | 23092 |
| rs139079833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116105 | TGCCTGTCTGTTTAT[A/G]TATGTGTGTATTGCT | 23092 |
| rs139086223 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016773 | GTTTTTTTAGGGTAT[C/T]GATTGATTTCTAAGC | 23092 |
| rs139091419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912641 | GCCCAGGAGACAAAA[A/G]TAAGCAAAATTTGAC | 23092 |
| rs139091960 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839493 | TGTGTCTGATGCTGA[A/C]ACCCATGTGGGATAG | 23092 |
| rs139104981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841211 | TTCATGTAGGCAGAC[A/G]AAGAAGAAAGCAATG | 23092 |
| rs139107351 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210971 | TGGAGAATAGGAAGC[C/G]AAAGAACCAATGATG | 23092 |
| rs139121133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152773 | GTAAAGAAGCCTGTT[C/G]TAGCCTCCTTAAAGA | 23092 |
| rs139126795 | in-del | -/T | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972470 | CCTTTTTTTGTTTTG[-/T]TTTTTTAATACAGGC | 23092 |
| rs139167165 | in-del | -/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162995 | GGTATGCGCCTGTGG[-/G]TCCCATCTACTTGGG | 23092 |
| rs139176027 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181148 | TACTGGCTCATTCTC[C/T]ACTCTGAAACCTGTG | 23092 |
| rs139181948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905780 | AATTGAACTCTTGCC[A/G]TTAAAAGTAATGGCT | 23092 |
| rs139184943 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065561 | GCATGTGAATTATTT[A/C]TCTCTGCCTGAGTTT | 23092 |
| rs139188845 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990972 | CCGTGTTGGGAGAAC[C/G]ACTACTCTCTTCAAA | 23092 |
| rs139191269 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087625 | CCTCATCTAATTAAC[C/T]CTGGCCCATTCTTTT | 23092 |
| rs139191372 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011900 | AGTAGAGTCCAAAGC[A/G]CTTGCATTGTGTTGT | 23092 |
| rs139209898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974676 | CAGGGCTCCGCTCCC[A/G]CCTGAGCTTTTCCTT | 23092 |
| rs139220454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869854 | AGAAAAGAAGGGCAC[C/T]TCCTCTAGTCCCTGA | 23092 |
| rs139226742 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800126 | AGAAAGAAATACCTG[C/T]GTAATAAGTAACTAT | 23092 |
| rs139229094 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947221 | TAGTTAGTTTTCACT[A/G]TAAATCTAAAGAGAG | 23092 |
| rs139235573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888290 | CTTTTCTACGTCTCT[A/G]TCTGGGGAGGGATGT | 23092 |
| rs139237055 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874677 | AGATGTGGCTTCCAA[C/T]GCCAGCAGCATTGTT | 23092 |
| rs139248144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171862 | GCATCTACTGATTAC[A/G]TTTCCCATTTACTGT | 23092 |
| rs139256229 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850042 | TTGGATCTTTCCTTC[C/T]CTTCCTCTGTGGAGA | 23092 |
| rs139256654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001836 | CAACAGAATAAAAGA[A/G]TGAATATTCTCAGAA | 23092 |
| rs139257077 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047927 | GCAGTGAGGTAGGAA[C/T]CTCCTACCTCCCAGG | 23092 |
| rs139260686 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931312 | CCCAAGGTCGTTTTT[A/G]TGGCGCAGTCTCTTT | 23092 |
| rs139312833 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106048 | ACAAGTTTACCAAGC[A/C]CAAAGGGTCTTTTTA | 23092 |
| rs139314433 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185854 | CCCAGCCACACTCTG[A/C]CTGCACTACCCCTCC | 23092 |
| rs139316966 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081067 | CACTGGGGGAGAAAC[A/G]GAGGTCTTGTCTTGT | 23092 |
| rs139317256 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001480 | ATATGTGATAAGGCA[A/G]ATATAGCAAAATATG | 23092 |
| rs139322929 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120312 | ACTCACAGGGTCAGC[A/G]ACTGTTGACCCTGTG | 23092 |
| rs139324792 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080826 | ACACCCAGTTGCTCT[A/G]TGGCAAATGAGCTGA | 23092 |
| rs139327280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898250 | TATATATGTATATGT[A/T]TGTATATATTTGCAC | 23092 |
| rs139332396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832001 | TTGGCCATATCATAT[A/C]CACCCCCAAATCTTC | 23092 |
| rs139336775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956903 | AGACTTACTATCATA[A/C]GAATAAGATGGGAAA | 23092 |
| rs139338939 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167519 | AAAAAAAAAAAAAAA[-/G]AAATCCATTGTTTGT | 23092 |
| rs139351997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784224 | CAGCATGCTTGTAAT[C/T]GGTTCCCCAGCAGGG | 23092 |
| rs139354316 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167022 | GGATAAAGAACTAGC[A/T]ACCCTTCAAATCCAG | 23092 |
| rs139356223 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121680 | GTGTCTTTATGGTCT[G/T]TCTTTTCTTTTGGGG | 23092 |
| rs139357845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216001 | GGGTCATATTAATTC[C/T]GTGTTTAAGTGTTTG | 23092 |
| rs139358671 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226589 | GCTCAAGACAGAAGA[C/T]CTTTTCTCCTGTTTT | 23092 |
| rs139362496 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845796 | TGACCCCTCACATCT[C/T]TCTTCTTGATAGACT | 23092 |
| rs139374406 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130221 | GGTATTTATGGATCT[C/G]CTAATTCCACTTACA | 23092 |
| rs139377014 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005007 | GACAGCACAGTTTCT[C/T]GTTCAACTTTGTTGC | 23092 |
| rs139382102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156439 | ACTGGTTCTCAGAGT[A/G]TGGTCCTGGGACCAG | 23092 |
| rs139391817 | snp | C/T | 0.000181236 | 0.00951761 | ARHGAP26 | 5 | allele_origin=T(germline)/C(germline) | 5:142932125 | GGATGGCCGGGAACC[C/T]GTAAGTAACAATTCA | 23092 |
| rs139413467 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983643 | AAAAATAAACTATAT[A/T]TTTTGACTGAAAGAA | 23092 |
| rs139417859 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141237 | GGCAGGAAAAAAGTT[-/A]CCAGCTAGACCCATT | 23092 |
| rs139422132 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075648 | GGGAACTACTGCTAA[A/G]GACAATATTGATTAA | 23092 |
| rs139422261 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118292 | ATTTAATCTGTACAA[C/T]ATTCACATGAAGTAG | 23092 |
| rs139437409 | in-del | -/TC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957833 | AGCGCTCTCTCTTTT[-/TC]TCTCTTACCCCTTCC | 23092 |
| rs139465573 | snp | C/T | 4.94181e-05 | 0.00497057 | synonymous-codon, intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207294 | ATCCACGTCCAGCGA[C/T]TCATCCCCCGTCAGG | 23092 |
| rs139478386 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934105 | ACTACTGTCTCTCCC[C/G/T]CTGCCTCCAATAAGC | 23092 |
| rs139479138 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159910 | ATTTTAACACTACCC[A/T]CTTGTGGTATGGGAT | 23092 |
| rs139481130 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026987 | GATGTGGTGTGTGAA[-/T]TTGGATATAGGGTGT | 23092 |
| rs139482044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218241 | GCCCAGCTTTTTCCC[A/G]TCACAGGGCCGTTGT | 23092 |
| rs139483888 | in-del | -/GGAAGGAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221923 | GGTGGGTGGATGGAT[-/GGAAGGAA]GGAAGGAAGGAAGGA | 23092 |
| rs139491070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861619 | GTCCTTTCATTTTTA[C/T]GCAGAAACAAATCAG | 23092 |
| rs139491117 | snp | A/G/T | 0.00358938 | 0.0422398 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815546 | TTTGCTAAGTGATGA[A/G/T]GGTCATGGATTCTTA | 23092 |
| rs139503133 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054091 | AACTTTTCTCGTGCC[G/T]TATCTTATTTTCTGA | 23092 |
| rs139503908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055491 | AAAAACCCTCAAGTT[C/T]ATGGTTAAACATACT | 23092 |
| rs139506787 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985180 | ATAAATACAAAAAAA[A/G]CTTGTTGAATAAGGA | 23092 |
| rs139526221 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092714 | GAAAACCTTTTAAGT[C/T]TGGGATTTCAATTAT | 23092 |
| rs139529017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160690 | GGGTCTTGCTATGTC[A/G]CCCAGGCTAGTCCCC | 23092 |
| rs139530030 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820933 | GACTAGCCTTCTGTC[A/C]CTCCACCTCCGCTAG | 23092 |
| rs139531853 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198973 | CTAGAAAACAGAACC[A/G]CTGCATTGTAAACTA | 23092 |
| rs139544039 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135469 | TGCCTTGAAGAGGAG[A/C]GGCTTCATATCTGGA | 23092 |
| rs139563690 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096533 | TTCAGCTTGCAACTC[A/T]GTCGCACAACTGCTT | 23092 |
| rs139565568 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162989 | GAGTGTGGTGGTATG[C/T]GCCTGTGGTCCCATC | 23092 |
| rs139565714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048617 | TAAACGAATTATGCC[A/G]TAGAAGACCTTCCCC | 23092 |
| rs139601518 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208424 | ATAATTTATGAAGCC[A/G]AGTTTCACTTTTAGA | 23092 |
| rs139605111 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043317 | GAACCTTTTGGGATT[A/G]GCATTGTTTTTCAAT | 23092 |
| rs139615323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048258 | GTGCATTTGTTTTTG[C/T]TGTCTTATGACTATT | 23092 |
| rs139618733 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946500 | TTCTTATAAGAGTGA[A/G]ACTTTGTTCATTTGA | 23092 |
| rs139635328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899427 | AATAGGTTTTGCTTA[G/T]GGTTATTCTTTTAGG | 23092 |
| rs139639308 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930644 | CTCCCTTCTCTTGCT[C/T]GTTTGCATGCTTTCC | 23092 |
| rs139639567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832621 | GGACATCTAGGGAAG[C/T]GTGGCCCCCTGATGT | 23092 |
| rs139642413 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007248 | TGTATTAGTGTTTGC[C/T]GAGCATTCTAATGTG | 23092 |
| rs139645587 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857559 | GCAAGGGAAGCATGT[C/T]AGGGTTTCTTTCTCA | 23092 |
| rs139659582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206229 | AATAGTTCAGCAGTC[C/T]GCTGAGATTCAGGAG | 23092 |
| rs139664108 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836428 | AGGCAGGAGCTCAAA[G/T]CCCTTTACCTGGGCT | 23092 |
| rs139668383 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951034 | CTTTCTCTTTCCCTT[C/T]CCCTTTCCCTTCCCC | 23092 |
| rs139674536 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924979 | TAATGATGACCTAGG[A/G]TGAAGCTCAGATAGA | 23092 |
| rs139677935 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835930 | TTTAGTATTACACCC[A/G]TTTTATATATTAGGA | 23092 |
| rs139678452 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853463 | CCCAACGTGCTAGGA[A/T]TATAGACGTGAGCCA | 23092 |
| rs139679794 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791141 | TGGAGTGTAGTGGCA[C/T]GATCTCGGCTTACTG | 23092 |
| rs139682298 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825868 | CAGAACACAGTTCTC[C/G]AATCTGCCTGTAACA | 23092 |
| rs139691218 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202767 | AGGCCTCAGAAATGA[C/T]GCCACACATCTACAA | 23092 |
| rs139697420 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812016 | TACTCATCACCTAGC[A/T]GCTGTGATGAGTTGG | 23092 |
| rs139699743 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207972 | AATTGCTCACGGCTT[A/T]TGCCTCGTTGTCCCC | 23092 |
| rs139718635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102317 | GTACCAGAGTGTGAG[A/T]CTCCCCTGGCAGGTC | 23092 |
| rs139726346 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103848 | ACCTAATGTAGATGA[C/T]GGGTTGATGGGTGCA | 23092 |
| rs139739056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152170 | ATACACAAGACATTA[C/T]GCATTTGTCAAAACC | 23092 |
| rs139740515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140163 | ATCTATATTTTTAAA[A/G]CACCCTAGTGATACT | 23092 |
| rs139748651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059506 | GTAGATCTTGAACAG[C/T]TGAACTTGTTCATCT | 23092 |
| rs139759612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101668 | ATTTCCCTGAAACAG[A/G]CACACACACTGTTGC | 23092 |
| rs139765809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939230 | CTGTGCTATTTTTGC[A/G]CAACACACAAAAAAT | 23092 |
| rs139784463 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140384 | CTGAGACCTGGAGTA[C/T]GTTACTTTCCTTTTC | 23092 |
| rs139786686 | in-del | -/A | 0.0607341 | 0.163335 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215496 | ACATACAATTTACCC[-/A]TTTAAAATGTACAAT | 23092 |
| rs139789386 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015532 | GGTCCACCCAGGGAA[A/G]AACTGTACATTTTGA | 23092 |
| rs139798853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912412 | TTGGGGATGTACTAG[A/G]AGGAGGGATGGATTG | 23092 |
| rs139801306 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800907 | TGCCAGGTTCATTTT[A/T]TGTTCCAGTCTAAGA | 23092 |
| rs139803583 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942911 | TCAGCCTCTGAGTAG[A/C]TGGTATTACAGGCAC | 23092 |
| rs139806441 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969017 | GCTCATTGTAGCCTT[A/G]ACCTCCCAGGCTCAA | 23092 |
| rs139808025 | in-del | -/GTACAAT | 0.152001 | 0.229992 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867345 | TGTTTGTTTTTGCTA[-/GTACAAT]GTACAATGCCAGGAG | 23092 |
| rs139811544 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938679 | TGCTATGGAAAAGAT[A/G]GCTCAGGAAGCCAGG | 23092 |
| rs139820010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866453 | ATGGTTGTGAGGATG[A/G]AGGGATTTAAAGTAC | 23092 |
| rs139824875 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034566 | CATAGAAAAGGAATT[C/T]TTCCCACAGCTGGGG | 23092 |
| rs139829859 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184296 | ATTACAAATATTCAG[A/G]CCTCCCCCTAACCTG | 23092 |
| rs139843424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918240 | CACCATCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 23092 |
| rs139860747 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207707 | TCCTGAACCAGACTC[G/T]GGTTTTGATGGCTCT | 23092 |
| rs139864033 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820187 | GTTCTCAGACCTCAC[A/G]TTGAGGAACACTGCT | 23092 |
| rs139865394 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953320 | CAAGCAAACAGATTG[A/G]TCACCTGCACTTATG | 23092 |
| rs139871897 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198493 | AAGTATTGTGAGCCA[C/T]GGTGCACAATAGAAG | 23092 |
| rs139884770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909005 | ATTTCATTATGATAG[A/C]CCTAGCTTTGATTTT | 23092 |
| rs139886587 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878966 | CAGAGGTGTTTCTTT[C/G]TTTATTTGTTTTTAA | 23092 |
| rs139888686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842086 | TTTAAATGGGAACAT[A/T]TGGTTCAGATTATTT | 23092 |
| rs139897729 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969519 | GCTTGATTTTATGTT[G/T]GCCTGTTCTTTAGAG | 23092 |
| rs139904086 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779455 | TGTGTGTTTTCTTTG[C/T]CAGATAGACAAAGGT | 23092 |
| rs139907602 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824139 | AGTATGTTGTGTGTA[-/TG]TGTGTGTGTGTGTAC | 23092 |
| rs139921203 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108758 | CTTCTTTATCAGTCT[G/T]TCCATCTCTCTGTAA | 23092 |
| rs139932235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096966 | GAAGCATGTCTGGGC[C/T]GGGTGCGGTGGCTCA | 23092 |
| rs139940891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087136 | ATTCAGAGTGTAGTC[A/G]CTACCTCTTTAGAGT | 23092 |
| rs139943980 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040231 | TTTGAAGTTTTTGAC[C/T]AGGGACTCCTAGTCC | 23092 |
| rs139949946 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143835 | TCCTTAAGGACCAAG[C/T]TCACATGCAGTTTGT | 23092 |
| rs139956452 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187536 | GCTTGTGGAGGAGGC[A/G]TGTGGAAGCTTTTTT | 23092 |
| rs139974213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084372 | GCTGATTGATTGGCA[A/G]TGGCTCATAGAAATG | 23092 |
| rs139976684 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152354 | TGTGTAAAACTTTCA[C/T]GCAATTTTTCTGTAA | 23092 |
| rs139991663 | snp | A/G | 0.00137897 | 0.0262218 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147410 | CCAGCTGCCTACCCC[A/G]CAAGGGCTTTGGTCA | 23092 |
| rs139992599 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108538 | CTTTGGTAGACTGGC[A/C]CTTGAAATAAAGCTA | 23092 |
| rs140011211 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894440 | CTCTAAGTTGTTGAT[G/T]AAGAGGTTGAGCAGC | 23092 |
| rs140011352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034467 | TAGGGCTTGAAAACA[C/T]TATGTTAAGTAAAAG | 23092 |
| rs140014255 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781678 | CAATTTGAATATTCA[A/G]ATAAACACTGATAAG | 23092 |
| rs140033531 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226956 | CCTGAGTTTCTATCA[C/G]CTGAAAATGGCAACT | 23092 |
| rs140053068 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882935 | GGAATAAATTTTAGG[A/T]TTCTAACTCAATCCT | 23092 |
| rs140063715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811614 | CAGAATCATGCCTTT[A/G]CGGAGCTTATATTCT | 23092 |
| rs140068435 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792570 | CCTCCAGGGTACTGA[C/T]CGTGCAGGGATCTAG | 23092 |
| rs140073672 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006938 | CAGGGGTGTTATTAA[A/C]AGTTCCTAAGCCTGG | 23092 |
| rs140074418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934350 | TTAAACACAAAATAA[C/T]TTTGTTTCTAAACAT | 23092 |
| rs140090684 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886250 | TTTTAAAATTTTAAT[A/G/T]CTTTTTGAACAGATA | 23092 |
| rs140097237 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890774 | GGTTTACATCATTTG[A/G]CCCATTTTCTCTTGG | 23092 |
| rs140099120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814378 | CCTAAGGAGATTCAT[C/T]GGTTTCCAATTCCTG | 23092 |
| rs140099149 | in-del | -/AC | 0.0607341 | 0.163335 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168864 | TTATTTTTACTCCTT[-/AC]ACAGAGTTGTTTTGT | 23092 |
| rs140099614 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821688 | ATTTATCTACACATT[A/G]AAATTTGAGAAACAC | 23092 |
| rs140109913 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949367 | ACCCGAGCCATATCA[C/T]TCACCAGTTCCAGTA | 23092 |
| rs140118147 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195984 | TCTAAAAAAATAAAG[A/C]TATTTAAAAGTTACC | 23092 |
| rs140133264 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142903650 | CACCATGGAGGGATA[C/T]CTCTACGTGCAGGAG | 23092 |
| rs140145944 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184898 | ACCTTTCTGGCAATA[A/C]GTGTTGTAAGCCTTA | 23092 |
| rs140151829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069778 | TTTAACTCTGTGATG[A/G]ATCTTGTAAGTGCCT | 23092 |
| rs140153485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138618 | TGAGTAGCAGTGGGC[A/G]GCTCTTGTCTGTAGA | 23092 |
| rs140166818 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119017 | GTCATTATCAGAACA[A/G]TTAAACAATAAAAGC | 23092 |
| rs140168335 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170829 | GGGTATTGGCAAGCT[A/T]CAGAAGCTGGGTGTG | 23092 |
| rs140171685 | in-del | -/GTTAGT | 0.0448719 | 0.142907 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098855 | CATTCAATAAATAGG[-/GTTAGT]GTTAAAGTATAACTT | 23092 |
| rs140181994 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994451 | GCTGTTAAGGGGTGA[C/T]GCAACCATAAAGGAT | 23092 |
| rs140183681 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950310 | TTTCCATGTTGGATT[-/A]AAACTGATTATATTT | 23092 |
| rs140184538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065859 | ACCTTTGGCCAGTGG[A/G]AGAAGGGAGCTGAGT | 23092 |
| rs140184844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944128 | CTCTAATGTGAGGGA[G/T]AAGTCCCTCTCTAGA | 23092 |
| rs140186570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134983 | CATTCATGCAGCTGA[C/T]GTTTACACGACACCT | 23092 |
| rs140205060 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003604 | TGGAAGTATTAAATT[C/T]TGTAGAATATAGACT | 23092 |
| rs140207306 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082249 | ACAATAATTATGTCA[C/T]CCTGGAGGTGTTAGG | 23092 |
| rs140224095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, splice-donor-variant | ARHGAP26 | GRCh38.p7 | 5:143208693 | CTTTCCTCCAAACAC[A/G]TGGGTAACCCCAACT | 23092 |
| rs140225755 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879731 | TAGAAACCACACCTC[A/G]TTTGTGTTATTATAA | 23092 |
| rs140226632 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900638 | ATGAGATTCCTTTAC[C/T]GTCACTTATTATAGC | 23092 |
| rs140236715 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834180 | GTAAGCTTAGCATGT[A/G]TCCAGAAAAGTACAC | 23092 |
| rs140248712 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111525 | ATTGAGGGAGTGGTT[A/G]TCCCTGGCTCACAGT | 23092 |
| rs140249988 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016178 | TAATGATTGAAATTT[A/T]AAAAAAATTAGGCTA | 23092 |
| rs140252097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142959330 | GATTAGCTTAAAACA[A/G]CCTCCATTTATGAGC | 23092 |
| rs140256373 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036779 | TGAGAAAATCTATTT[A/T]AAGCACTTACCCAAC | 23092 |
| rs140263300 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145924 | TTTACATACATGACT[C/T]GTGCAAAGGGAAAAG | 23092 |
| rs140275712 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786121 | AACTACTGGCTTTTG[C/T]CACTATGCCTGGCTA | 23092 |
| rs140287127 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144315 | GCTGCCTGTTCTTGT[A/G]CGCTTCTGTCAGGAG | 23092 |
| rs140288221 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195182 | GGTATCCGGACCAAG[C/G]TTCGTGCATTTGCAA | 23092 |
| rs140311051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207040 | GGACGTGGAGATTTG[A/G]TCTGGAGGAATGTGA | 23092 |
| rs140320627 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884163 | TCCAGCTTCCTTGCC[G/T]GCTCTCCCCGTTGGA | 23092 |
| rs140337614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031516 | TGGGAGGTAAGAAGT[C/G]GTGCCAAGGGTGATA | 23092 |
| rs140345117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816113 | CCTCTGTGCTTCTGT[A/G]GGACTCTGATTCTTT | 23092 |
| rs140345280 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142770275 | TTGGATCAAGACCGC[A/G]GAAGGGCCGGGCGTC | 23092 |
| rs140352973 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191674 | AAACGTCATGAAGGT[G/T]GGACACTCATGACTG | 23092 |
| rs140362436 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127346 | TGTGTGTGTTCATGT[A/G]TTATGTACCACAGGC | 23092 |
| rs140371844 | in-del | -/TTTCT | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869176 | CTGAGCTGTAATCAC[-/TTTCT]TTTCTTTTCTTTTTC | 23092 |
| rs140375292 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115078 | TGGCTTATGCCTGTA[A/C]TTCCAGCACTTTGGG | 23092 |
| rs140382439 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995830 | TGGAATACTATGCAG[C/T]CATAAAAAAGAATGC | 23092 |
| rs140382803 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040680 | TTGCATTAGATTGAA[A/G]CGGTTGCATTTAAGC | 23092 |
| rs140386849 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920710 | GCAAGGATATTTAGT[G/T]CTGGAGTTGTAATAA | 23092 |
| rs140393309 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078461 | TTCCCTCGGCTGTGG[A/G]CACTGATGGACCGTG | 23092 |
| rs140402247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088156 | CCATTTTATGTGCTT[C/T]TGAGATTATATATCT | 23092 |
| rs140422845 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991430 | TAAGGTGATGCCTTG[C/G]CCTGCTTAGGCTCAC | 23092 |
| rs140427923 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927010 | TGAACTGCTCTATGC[C/T]ACTGTTCTTTAAAAC | 23092 |
| rs140453479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775497 | TATACATAACACAAC[A/G]GTTACCACTTTAGTC | 23092 |
| rs140455783 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220217 | CTTTATTCTTTCTAC[A/G]TTTTTATTTTGGAGA | 23092 |
| rs140465926 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066562 | CGGGAGAAAGAAGAT[A/G]ATAGAGCTGGTTTTA | 23092 |
| rs140478116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866806 | TGCATGTTATGTAAC[A/G]TACCGTGGCTGATGT | 23092 |
| rs140487561 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795605 | GTAGAATATGTACTT[A/G]TTTTGCTTCCAGCCC | 23092 |
| rs140496809 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881421 | TACTGTCCCCCGGGG[C/T]GGCGGCTGGGGGGTG | 23092 |
| rs140498812 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131906 | AGCTTCTTAGAGGTT[C/G]CAGTCCTTGAGCTTT | 23092 |
| rs140506936 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196442 | AGAGTGAGCTTCCTG[C/T]AAGCCCCTGGTCACA | 23092 |
| rs140508759 | in-del | -/TATC | 0.0146672 | 0.084371 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768780 | TTTTTGGGTTGTAAT[-/TATC]TATCAGATAGCTGTC | 23092 |
| rs140516115 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843589 | AATCCCTGTTTTTCT[G/T]CAAGGAAGCTGAGGG | 23092 |
| rs140517398 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869433 | ACTATGTTGGCCAGA[C/G]TGGTCTCGAACTCCT | 23092 |
| rs140539165 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094252 | ACCAAGGAAATACCT[A/T]ACTGCCTCCCGTGGC | 23092 |
| rs140551119 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017531 | CTTTCGTTTCATTTT[A/G]TTTATTCATCCATTC | 23092 |
| rs140559694 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216542 | AATCCAACCTGCCAC[C/T]TGTCACCTAACAATT | 23092 |
| rs140567669 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128540 | AAACCTCTGCAGTTA[C/T]AGCCTCTGAATTTGG | 23092 |
| rs140571225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193530 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 23092 |
| rs140588319 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123505 | CTTTAACCATCAAAT[A/C]CAGAGCAATTTTATG | 23092 |
| rs140589439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050689 | TGAAGACTGGAGCCT[A/G]CTGGAGTAGGGGAAC | 23092 |
| rs140595453 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975447 | TGTCTGTCTATTTTT[G/T]ATAAAAGATATTCTG | 23092 |
| rs140598877 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949586 | AGACTTTTCAGTACA[A/G]TGTTCTAAACTCCAG | 23092 |
| rs140600387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018842 | TTCTGTATAAATTCT[A/G]TAATAAGTTTAAGAA | 23092 |
| rs140602470 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979654 | AAGGAAAAAGGAAAA[C/T]GCAGAAGTGGAGGCC | 23092 |
| rs140605394 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925395 | GGATTAAAGAATTTC[A/T]TATCCAGTTTCCCTA | 23092 |
| rs140612062 | snp | A/C/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009077 | AGAGCTACTCTCCCC[A/C/G]CCTGGTGTTTATCGT | 23092 |
| rs140639149 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838571 | TTTTGCTTTTATCAT[A/C]TTGGACAATAATGCC | 23092 |
| rs140642076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983160 | TGATCTCTGAGCCTT[A/G]TCTTCCCTTGCTACC | 23092 |
| rs140644087 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903288 | CTGAATTGATCTGTA[A/G]GAGTGAGGGCTGGGC | 23092 |
| rs140644967 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868760 | GAGTTTTGTTTTGAG[C/T]GTGTTGAGTTTGACC | 23092 |
| rs140649805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797054 | TTGCAGAAGGTTTAG[A/G]TGACACAGTGAAGAG | 23092 |
| rs140653642 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928203 | TTCAATATTTTTTCT[G/T]TATGATTAGGACTTT | 23092 |
| rs140662422 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997308 | GTGGTGAAACATTTT[A/G]ATCATCCACTGTGCA | 23092 |
| rs140673908 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828801 | AGTTGCCACCTGGCC[C/T]ATCTGTAGAGTGGCC | 23092 |
| rs140698637 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097067 | ATACAGACCATGCGC[A/G]GTGGCTCATGCGTGT | 23092 |
| rs140704199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021532 | GGTAGATTCCGCCAC[A/G]TGGATTAGAGAGAGG | 23092 |
| rs140704675 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982184 | CACCTCCCCATCCCC[C/T]AAGGCAAAGGTGGAA | 23092 |
| rs140706061 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142118 | GATCAAAACAACAGA[C/T]TGACTCTACTTTTCA | 23092 |
| rs140710866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901802 | CCTGGCACACAATTG[A/G]TGCTCTTTAAATGTC | 23092 |
| rs140732846 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904955 | TTTGTTTGGACTTAA[G/T]TTTCCTGGTAACTGG | 23092 |
| rs140749961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999038 | TCAGGACCTAAAGGG[G/T]TTCATTCATGATGGT | 23092 |
| rs140781205 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109317 | ACACAGATATATAGG[C/T]GCAAAGGCACAGGGC | 23092 |
| rs140782907 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041430 | ATAAAGTGTCTTTTT[C/G]TGTTGTATGAATTTT | 23092 |
| rs140785303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176154 | AATGAAATATGACAC[A/G]TGACAATGAAACAGA | 23092 |
| rs140788641 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940041 | TGGAAAATGTGATTT[C/T]GTTTAGCAGTCAGTG | 23092 |
| rs140794309 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115299 | GATCACGCCATTGCA[C/T]TCCAGCCTGCACGAC | 23092 |
| rs140794466 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181679 | CAAATGAATTACACC[A/G]GAATAGATTTCTGGA | 23092 |
| rs140809131 | in-del | -/T | 0.0689305 | 0.172377 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972866 | ATTTGACCTTTATTC[-/T]TTTTTTTTTTCAGAT | 23092 |
| rs140810210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891217 | AGCCACACGATGCAG[A/G]GGGTGGTGGTGGTGA | 23092 |
| rs140811918 | in-del | -/A | 0.179744 | 0.239925 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030601 | CCTTTATATCATCAC[-/A]AAAAAAAATGAGAAA | 23092 |
| rs140815765 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822027 | CTGTTAAACATACTC[C/G]AATCCCCCATAAAGC | 23092 |
| rs140819500 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113443 | CAGTACAGCCTGGAT[C/G]AATGCATATATGGCC | 23092 |
| rs140821394 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070953 | GACATTCTTCACAAA[C/T]ATAGAAATAAAAAGT | 23092 |
| rs140826444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179233 | AGCTTTCCCCCACTG[A/G]ACTGCACACTCCTCA | 23092 |
| rs140831664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078968 | GATATCTTGATTGTG[C/G]TCTGCAAATGCAGAG | 23092 |
| rs140839324 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164311 | AGGGGAAGTTTTACT[A/G]TCAAATTTTCATGCA | 23092 |
| rs140849632 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098214 | CATAAGTTCTAATGT[G/T]AGGGTTCAGACCATG | 23092 |
| rs140854815 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995456 | GCAAATCAAAACCAC[A/C]GTGAGATACCATCTC | 23092 |
| rs140858071 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112580 | CTAATCTTGTAAAAC[C/T]GAAGCTCTGTATCCA | 23092 |
| rs140864428 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178161 | CATGCCACCATGCCC[G/T]GCTAATTTTTGTATT | 23092 |
| rs140864580 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212823 | CAACCCTCACTGCAC[A/G/T]TTGGAATTACTTGGA | 23092 |
| rs140895707 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849314 | CAAAAAGACCCAAGA[C/T]TTCAGAGCAGGGGAG | 23092 |
| rs140897412 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219517 | CTATGTGGAATGTAC[C/T]ATGAGCATTTTAGGT | 23092 |
| rs140903672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774867 | TGGCTTTTTTTCACT[C/T]AGCAATGTGTACTGA | 23092 |
| rs140931093 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852737 | GGAGGTCTGTGTTTC[C/T]CTGGAACTCTGTCAT | 23092 |
| rs140935168 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221682 | CACGCTCCATCAAAC[C/T]TAGGTAGTTTTTGTA | 23092 |
| rs140942877 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192516 | ATTTTAAATGGTTAT[A/G]TAAGTAGCTAAATAA | 23092 |
| rs140962124 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025197 | ATTTGATTTTCACAA[C/T]ACCTGCATCTTATAT | 23092 |
| rs140965860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920425 | AAATTTCTCACAGAT[A/G]TAAGTGACACGTGGA | 23092 |
| rs140986575 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914588 | TTTGCTAATAGCTTA[C/T]CCTGCGTGCTCCTCA | 23092 |
| rs140988712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847065 | ATCTCAGCTCTGTTG[C/T]TTGCTCTCGGTGCAC | 23092 |
| rs141010445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805622 | GAAAAATGAGTTTAT[A/G]TGAAGGCCCAAAAGT | 23092 |
| rs141011038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854235 | TTATTTCTCTGTTGC[C/T]GATAAACCACTTCCA | 23092 |
| rs141011174 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810017 | GAGTAAAAGTGTTTA[C/T]CTCTCCCTGGAGCAG | 23092 |
| rs141011957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957749 | CCATGACCCAGAGTT[C/T]AGCTTAAGTACAGAG | 23092 |
| rs141033574 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224007 | AGCCCCTTGGATGGC[A/G]GCGTTGCTTCAGAGT | 23092 |
| rs141047042 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962919 | CTAAGCCTAGTACCC[A/C]ATAGTTATTTTTTTC | 23092 |
| rs141071415 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157507 | TTGACTAGAGAACTT[C/T]TGAGCCTTTAATATG | 23092 |
| rs141082130 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936005 | GTCCTAGTCAGTGCA[A/G]TAGGGCAAGAAATTA | 23092 |
| rs141090121 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863920 | ACTGCCTCCTATCTG[C/T]GCACCTGCTTGGTGT | 23092 |
| rs141092685 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910330 | TTATACTTCCCATGA[C/T]GTCACTATTTCCTCA | 23092 |
| rs141099038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045378 | CATGATTCTCCCTAC[A/G]AGTTAAATAAGTTTG | 23092 |
| rs141099476 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142959977 | GATTGGTCTGTTTTT[A/G]TATTCCAAGGGCCCA | 23092 |
| rs141106396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976541 | GAGTCTTTAACATCC[A/G]TACATAATAGATGTA | 23092 |
| rs141113007 | in-del | -/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785530 | GTAATTGGAACGAGA[-/G]CGTGTTATTTCTGCT | 23092 |
| rs141114086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871115 | ATTACCTAATCGTCT[A/G]TCGGGGGATCGGCCT | 23092 |
| rs141119428 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801927 | AGAGTTGCCTTCTGT[C/T]TGGTGAGACTGGAGT | 23092 |
| rs141123015 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035921 | AGCTTGAGCGACAGA[A/G]TAAGACCTTGTCTCA | 23092 |
| rs141131459 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822612 | TGATATATATGTATA[A/T]GTATAATATATATAC | 23092 |
| rs141146179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201320 | ACTCTGAGGGTTGTA[A/G]GAATGCCTTTAGCAG | 23092 |
| rs141152198 | in-del | -/AATA | 0.0256519 | 0.110308 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901175 | CAGGGAGGGGACATT[-/AATA]GTTTTTAAGTATATG | 23092 |
| rs141152666 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220942 | TCGGAGCGGAAATGC[C/T]TTTCTAAAACAAGCT | 23092 |
| rs141152725 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778135 | GCACAGCATATGGGC[G/T]ATGAGAGAAAAGAAA | 23092 |
| rs141161030 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162937 | ACCAGCCTGGACAAC[A/G]TGACATACCATCTCT | 23092 |
| rs141169946 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068078 | CTGAGGTACGAGAAT[C/T]GCTTGAGCCCAGGGA | 23092 |
| rs141196602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882087 | GTACATTTGGAATGC[C/T]GGACTCTAGAATAAG | 23092 |
| rs141197496 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045093 | AGCAAAAGAGTGGTT[A/C]TGAAAGGATCTTGTT | 23092 |
| rs141198691 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222906 | ATAGGCACTCTCTCT[A/G]CCCCACCTCTCAGTA | 23092 |
| rs141215550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975171 | TGAGCAAGGAGATGT[A/G]GCATCTGCTTCCCTT | 23092 |
| rs141216321 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163702 | GTGATCCATCCACCT[C/T]GGTCTCCCAAAGTGC | 23092 |
| rs141237190 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799995 | CTGATGTAGTGGGAC[A/G]CACAGTGTTAAACGA | 23092 |
| rs141250885 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980964 | GTAGTTGTCATTGTC[A/G]TTGTAGTGTCACACT | 23092 |
| rs141252856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932654 | AAGGTTGCAGAAATT[G/T]TAAGAGTACAGTCTA | 23092 |
| rs141255779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127943 | GAAGCTAATCTTGTC[C/G]TGTGGTCATGGCTTT | 23092 |
| rs141258686 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217473 | TCATCTTGAAGCAGC[A/G]TGATTCGTGATACCT | 23092 |
| rs141259424 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085068 | AAAAAAAAAAAAAAA[-/G]AAACGCTTTCTGCAC | 23092 |
| rs141260850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859857 | GAAGGCTATGATAGG[G/T]TTCCTGGGCCGTTCA | 23092 |
| rs141261873 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057155 | TTCTAGCAGGCTGGT[G/T]GTCATATGTGACTTG | 23092 |
| rs141277017 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162071 | CTTGCGCAATGCTGC[G/T]GGAAGGTTGGTAAAT | 23092 |
| rs141277545 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143054444 | TTCATTTTAGACCCC[A/G]AGACTGCTTCTGAGA | 23092 |
| rs141297355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889117 | TTTCCTTTGGGAATG[C/T]ATTGAGTTATGCATT | 23092 |
| rs141302843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053766 | AATCATACCACAGTC[C/T]ACCACTTTAACCCAA | 23092 |
| rs141303121 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125178 | TCTTTTTCAATAGAA[A/G]GTAAGAGACCTCTGT | 23092 |
| rs141320466 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776351 | TAGTCCTGTTTTAGA[A/G]CATTTTTAGCACCCC | 23092 |
| rs141322736 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023447 | TGGGCCACTATTTTT[A/G]AAAGACATCTAAAGC | 23092 |
| rs141324688 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951510 | AAGGAGGATCAGTCT[A/G]GGATTTGGGCTGGGG | 23092 |
| rs141325657 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102772 | CTGTTTAAATTAGTT[C/T]TCCTCCTCCTTCTCC | 23092 |
| rs141327251 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901484 | CACTTCCTTTTCTGC[C/T]TTCCTCTTCTGTGTA | 23092 |
| rs141327941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169081 | GCCTTTGCTTTTGCA[A/G]TGTTTGCATTTCTCT | 23092 |
| rs141332341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834278 | CAAGCAATAAAAATG[A/G]TTAGCATCCTGGAAA | 23092 |
| rs141343217 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851776 | CCAGCCACATGGTCT[A/T]GTGCACCTGGTGCTC | 23092 |
| rs141353395 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837932 | CCTGCAGGGATATTG[G/T]CAGATAGCAATCTGA | 23092 |
| rs141361386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906104 | GTTTCTTCATGATTA[A/G]ATTTGGATTATGCAT | 23092 |
| rs141362717 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209315 | CTGTTTTTCCTTCCT[A/G]CTTCTTCCTACCTCC | 23092 |
| rs141368386 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172676 | GCTGAAGTATTGAAA[G/T]GTTGTTTTTACTATG | 23092 |
| rs141373215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840428 | TACATAATCACTGTT[G/T]TTGTTGTTGTTGTTG | 23092 |
| rs141393543 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203568 | CCAGCAATCCCACTA[C/G]TGTGTATACACCCAA | 23092 |
| rs141394821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831866 | TTTCTCTCTCTGCTC[C/G]TTGCAACATAGCTAC | 23092 |
| rs141398585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130613 | TTTGATTCTCTTGAA[A/G]TCATCCCTTCCAAAA | 23092 |
| rs141406794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061011 | AGTTTTGACTTTCCA[A/G]GTCTTTGCAATTTGA | 23092 |
| rs141406822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014511 | TGTTGCCTCCAGCAC[A/G]GTCTCGCTCAAAGGA | 23092 |
| rs141412022 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116124 | GTGTGTATTGCTTGG[C/T]AAAATATACTTCCTA | 23092 |
| rs141412357 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042987 | AAAATTAAACTTTTC[A/G]TTTTGAGATAATTGT | 23092 |
| rs141432758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001105 | TGTAAGTCTGTTTGT[A/G]TAGTGATCTAGAATA | 23092 |
| rs141445118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017214 | AATGTTCTGAAGGAG[C/G]AGTTAACAAAAGGGA | 23092 |
| rs141445476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154515 | TCCAGTCCCTCAGCC[A/G]TGGTATGTATTTTTC | 23092 |
| rs141448092 | in-del | -/C | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184345 | TATCCTTTTGTCTCT[-/C]CCGTAAAAACATGTA | 23092 |
| rs141448715 | snp | A/G | 0.0015105 | 0.0274402 | intron-variant, missense | ARHGAP26 | GRCh38.p7 | 5:143057913 | TTGCAGTGGAGAACA[A/G]CAGCAAATGCCAGAT | 23092 |
| rs141449724 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917725 | TAGAGGTGGGTGGGG[-/G]TCTCCTCATGTTGCC | 23092 |
| rs141453005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944557 | TGCATTTGATGAGCC[C/T]GTAGGTGTATTTATA | 23092 |
| rs141471522 | in-del | -/CTT | 0.202959 | 0.245534 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033791 | TTCTCTCCCAGACTT[-/CTT]TGATTCTCATTGCTA | 23092 |
| rs141480403 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869300 | CAGCCTCAGCCTCCC[A/G]GGTTCACGCGATTCT | 23092 |
| rs141482301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828163 | ACCTCCCTGGGAGCC[A/G]CTGGCAGATTGTATG | 23092 |
| rs141492662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215366 | CTCCTGATCTCAGGG[A/G]CAGAATTGTTTTAAA | 23092 |
| rs141497396 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893357 | AGCACCTACATATGA[A/T]TAAGAAGATGTGATA | 23092 |
| rs141499941 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913994 | AAGCTTATTTGAGCT[G/T]CCTGTTCAAGATCAG | 23092 |
| rs141501740 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824063 | CATGCACATTTGGGG[A/C]CCAGCTCCACAATGG | 23092 |
| rs141506501 | in-del | -/T | 0.304438 | 0.244001 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087563 | AGACATGCTCTCCTC[-/T]CTCTGACCCTAGGGC | 23092 |
| rs141513058 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202219 | TCTTTTTTCATCTTT[A/G]TTGGTTTTAAGTGTT | 23092 |
| rs141517756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107538 | AGGCAAAGCAAGATG[A/G]CAGCAACTAAGATGT | 23092 |
| rs141520247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112863 | TCTGTTCATCCATCA[A/G]TAGACATTTGGGTTG | 23092 |
| rs141522172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783871 | TTTTCTTGCATTTGT[A/G]TCTGACTAGTGCACT | 23092 |
| rs141541115 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074340 | ATTATAGAACTTTCT[A/C]TTCTCTTTTACTTCT | 23092 |
| rs141545063 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996473 | ACTCCAACCTGGGTG[A/G]CAGAGCAAGACTCTG | 23092 |
| rs141549779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805434 | TTCTCCAGTTCATAG[A/G]CATTTGGATCATTTT | 23092 |
| rs141558472 | in-del | -/A | 0.0614824 | 0.164198 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933357 | GAAATAAGTGCTGTG[-/A]TTCCATTTTATAGAT | 23092 |
| rs141573103 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993106 | CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGTTAC | 23092 |
| rs141579433 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916274 | ATACATTTATCCTTT[A/T]TACTTAATGCTGATA | 23092 |
| rs141583833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937774 | AGCATTATGCTAAAT[C/G]AAAAAGGCCAGTCTC | 23092 |
| rs141585440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103714 | AAAACCAAACACTGC[A/G]TGTTCTCACTCGTAA | 23092 |
| rs141597951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028288 | GTTGTTACCACTTAA[C/T]GTGAGTCTGGCTTTC | 23092 |
| rs141627465 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983225 | TATGCTGGTTCGTTG[-/T]TTTTTTTTTGAGATG | 23092 |
| rs141627550 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025671 | ATTCTGATTTGGAAT[A/T]TTAAGGTGGACTAGG | 23092 |
| rs141631142 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194789 | AAGTTTTTTCCAGTC[A/G]AGTCAATAAGCTCCT | 23092 |
| rs141631212 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954784 | AGATCTAGCCCTTTG[C/T]CCTTATGGAGACACT | 23092 |
| rs141641205 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990864 | TGTATCAGTTGTCAG[A/T]CGGCCCCTACTGAGT | 23092 |
| rs141641273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032595 | AGCTTGGTGGTGATA[A/G]TGTTCTAAACCTTTT | 23092 |
| rs141646560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027491 | ACCTGGCTGACTTTT[A/T]AAATATATACATATA | 23092 |
| rs141653937 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183092 | AAAAAAAAAAAAAAA[-/G]AAAAAAAAACCTCAT | 23092 |
| rs141655558 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912421 | TACTAGGAGGAGGGA[C/T]GGATTGCCAGGGGAT | 23092 |
| rs141664876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031148 | CTTGAAAGACAGCCA[A/G]TGTGGCTAGGTGCTC | 23092 |
| rs141668512 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911057 | ACCCACTGTTCTCAT[A/T]GCTTCAGATCTGGAG | 23092 |
| rs141670264 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917468 | ATTGGCACCCTGTCA[C/G]TTGCATTTGGCATTG | 23092 |
| rs141677310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849264 | TAGGTGTGGACTCTT[G/T]TGTTCTCACTCTTGG | 23092 |
| rs141681559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817868 | CTTAAAATTCCTGGA[C/G]AGAACCTGAAATCTA | 23092 |
| rs141719534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155868 | GCCCTGACATACACA[G/T]TACATGCTTAAAGCT | 23092 |
| rs141729262 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194052 | GCCCTGCAGTGAAAT[C/T]AGCAGGACACTGGAC | 23092 |
| rs141737730 | in-del | -/AG | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136428 | ATGACCGGAGCATAC[-/AG]ATATGCTCAGATATT | 23092 |
| rs141741560 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087234 | TCAAATTAAGGTGTT[G/T]TAAGCCTCCCCTGTT | 23092 |
| rs141749997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153647 | GATTGAAAGAAAGCT[A/G]GGAGGGCTGGGATGA | 23092 |
| rs141750011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191900 | ATATGTGGAGCTGTC[A/G]TGACAACACCAGAAT | 23092 |
| rs141771018 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990568 | TTTCAGCTTTTCTGC[C/T]CTGGTTTCTCCCCAT | 23092 |
| rs141780029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912249 | AAATAAGCCCTTGAT[A/T]TGCACAACAATGTGG | 23092 |
| rs141781741 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091586 | ATGACTTTTATACCA[A/G]ATAAACTAAATTTCA | 23092 |
| rs141782931 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089113 | TAAATTTAAAACTTA[C/T]ATCTAACAATCCCTC | 23092 |
| rs141783390 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884855 | TGGGACAGTATTAAG[G/T]CTGGATCTAGCCTTA | 23092 |
| rs141786309 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813656 | CCCAGTATCTTCACA[C/T]GGTCTTTTCTCTGCT | 23092 |
| rs141797534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041542 | CTCTTCAGATGCTGC[C/T]TTTGGCAAGAGAAAG | 23092 |
| rs141798024 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873805 | CTTCAACCATAGTAC[G/T]AAGAGCTTAGAGCAT | 23092 |
| rs141802352 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804407 | TCATTCACTCACCCA[C/T]TCACTCATTGGCTCA | 23092 |
| rs141809309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158554 | TCATTATGGCAAAAG[A/G]GAAAAGAGCTTCTGA | 23092 |
| rs141816030 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189297 | GTTTTAATCCTAAAT[A/G]TTTAACCATAAAAAA | 23092 |
| rs141821635 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793775 | GTATTTTAAGTAGAT[A/G]CGGGGTTTCTCCATG | 23092 |
| rs141835204 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878326 | ACAATTCAGCCCACT[C/T]GTTTTGCAGATGACG | 23092 |
| rs141846274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806741 | CTTAGACATCTAACT[C/G]TGTGTTAATATATGC | 23092 |
| rs141857508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876602 | AGGCAACATAGTGAG[A/T]CCCCATCTCAACAAA | 23092 |
| rs141862779 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968224 | CACAGAGAGATTAAG[C/T]ATTTTACCTAAATTC | 23092 |
| rs141865369 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085443 | GGGAAGAGAGTTCCA[C/G]TTAATGGCATGTGTG | 23092 |
| rs141872257 | snp | A/G | 0.000693149 | 0.0186036 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143121118 | TTTCAGAACATTGTC[A/G]TTGAGATCCTAATAG | 23092 |
| rs141874731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881522 | ATATTCTATTCTCCT[A/G]TTCATTAAACCATGA | 23092 |
| rs141877410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017943 | TGTATTGTTCTCCAG[A/G]GTGGTCGATCCGCAG | 23092 |
| rs141887162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810595 | ATGGCATACCTGAGT[A/G]GACAGGCAAGTTGCA | 23092 |
| rs141893898 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005804 | AGCAAGAACGCTTCC[A/G]GGGCTGTTAAAAGAC | 23092 |
| rs141895291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982531 | ACCATTGTACAGCCT[A/G]GCAGTCCTGTGGAAT | 23092 |
| rs141896465 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190753 | CTGGGAAAATATATT[G/T]GCAAATATTATCACT | 23092 |
| rs141903444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902263 | CCCTATTTATGTTCT[C/T]GGAAGTGCTGCTGCT | 23092 |
| rs141903840 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809296 | GAGAGAGAGGAAAAG[A/G]AAAGAAAAAAATATA | 23092 |
| rs141912085 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974929 | TCTCATACTTTTCAT[C/T]CCACCTGAAGAGTGG | 23092 |
| rs141914570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186864 | TTTTCTCTCTTTCCA[C/T]TTGGTTGCATGATGA | 23092 |
| rs141921082 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933334 | GTTTATTTCTCTTAG[C/G]ACTTAATGAAATAAG | 23092 |
| rs141924468 | snp | A/C | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860701 | TGTTTCCTCCTCCCA[A/C]CCCTGCTGTCACCTA | 23092 |
| rs141927975 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229270 | CTTCACATTTCTAAC[A/G]TTCTTCTCTTAGAAT | 23092 |
| rs141940546 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080565 | CCAGGAAGAGGGAAC[A/T]GCAAGTGCAAAAACC | 23092 |
| rs141943486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146558 | ATGACTGCTGGGACT[A/G]TGGACTCAAGTGTTT | 23092 |
| rs141946058 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198347 | TTTCTTACAAATAAA[A/T]TCACATATTGTGAAA | 23092 |
| rs141949572 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090857 | CTGGGGTCTTTATCG[A/T]AATCTCCCCAGATTA | 23092 |
| rs141957043 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134849 | TTATGCGAATTAAAT[G/T]AAATTATGCATTTCA | 23092 |
| rs141959771 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228110 | AGGTTAAGACATTCT[A/G]TACTGTTCTACGTCA | 23092 |
| rs141964978 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033661 | TAGCCTTTGTCTAGG[C/G]CAGAAGTTCGTCAAT | 23092 |
| rs141967991 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961278 | GGAGGATTGCTTGAG[C/G]CCAGGAGTTCCAGAC | 23092 |
| rs141969621 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787578 | ACAGCTGACAAAGCC[A/G]CTGACAAAGCCAGCA | 23092 |
| rs141977348 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182349 | TTGCAGATGATGAAC[G/T]GGGAAACTCCATAGG | 23092 |
| rs141989002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977961 | TCAGCCCATGGCTGG[A/G]ATGGTTGACAGATCA | 23092 |
| rs141996566 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086483 | ATCTTTATTTTTAGT[A/G]TATCATGTAAGCAAG | 23092 |
| rs142014577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010293 | AGGCAAGATAGAATA[A/G]TACACCACTGACCAG | 23092 |
| rs142034437 | in-del | -/A | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213299 | AAGCAAAAACAAACC[-/A]AAAAAAAATGCCTCA | 23092 |
| rs142035911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833664 | GCTGATATTTGCGCT[C/T]TTTCTGTGTGAGCAA | 23092 |
| rs142040376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008461 | TGTTGTTTTAAGATG[C/T]TGACACATTGCCTTA | 23092 |
| rs142041417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014809 | TCTCCTTGGTGTATA[G/T]GAGAAAAAACAAAAT | 23092 |
| rs142052977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118738 | GATCATGCCACTGCA[C/T]TCCAGCCTGGATGAC | 23092 |
| rs142053664 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894473 | TGACACTGTCCCTTC[C/T]GTAAGTATCAGTGCT | 23092 |
| rs142057997 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044829 | GGTTGTAATAGATCA[A/G]GCAAGGCAAACCCTA | 23092 |
| rs142093137 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060507 | AAATGATTACCAGGG[C/T]ACATCCAAATCACAG | 23092 |
| rs142115396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943570 | GCCCTACTTTCTGTT[A/G]TCATCACATTAATTA | 23092 |
| rs142119976 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138886 | ACGCTCAGGGTTACA[C/T]GGCAACAACGTAGAT | 23092 |
| rs142124555 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845337 | GGTATTTGTTATCAC[C/G]CTGCTTCACAGATGA | 23092 |
| rs142129688 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216399 | TCCCATTGCTCTGAG[A/T]ATTACTTACAAGGCC | 23092 |
| rs142139828 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156864 | CAGGGCTGCACTTTC[C/T]ATCTCCCCCCAAAAG | 23092 |
| rs142146804 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204482 | TGAGCCAAGATTGTG[C/G]CATTGCACTCCAGCC | 23092 |
| rs142149250 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180345 | TGGCCAGGATGGTCT[C/T]GATCTCTTGACCTCG | 23092 |
| rs142153162 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114500 | TTAACAGCCCTGGAA[A/T]CTAAACTTGTCTGGT | 23092 |
| rs142158613 | snp | A/C | 4.98484e-05 | 0.00499216 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143147363 | TGGCTGTGGTCAAAC[A/C]CACCCGGCCCAACTC | 23092 |
| rs142158861 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143118 | TCTTAGGCACCATGG[A/G]AAGTTGGGATATTAG | 23092 |
| rs142163294 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011804 | AATTACACAACCTCT[A/G]TGTCAGCCTCCACCT | 23092 |
| rs142168181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136853 | GTTTGGCATTAAAGT[A/G]CAGGTAACGATTATG | 23092 |
| rs142172254 | snp | A/G | 4.95389e-05 | 0.00497664 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143121008 | CTAACAACCACAAGC[A/G]GAATTTGATGACGGT | 23092 |
| rs142173566 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077674 | CACAGATGACAGGGC[A/G]CTGCCAGCGTCTTTG | 23092 |
| rs142180371 | in-del | -/TCC | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881861 | GCTAAAATTACTTTT[-/TCC]TCCTCCTCCACTCTC | 23092 |
| rs142180649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997828 | TAATGCTGATATCGT[A/G]TCTAAGTGAAAGAAG | 23092 |
| rs142190778 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895198 | GTACAAATAAGATTC[A/T]CTACCTAGATTTAAG | 23092 |
| rs142197039 | in-del | -/T | 0.0618563 | 0.164627 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962736 | GAGCCATGTGAACTG[-/T]GGGTAGAACAGAGGG | 23092 |
| rs142205773 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141191 | CACGTTGATAATGTG[C/G]CTATTAAAAAATGAT | 23092 |
| rs142210981 | in-del | -/TTGA | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894126 | TCTGTGTAATGCTAT[-/TTGA]TTTGTTTTTGAAAAT | 23092 |
| rs142215820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071275 | ACTGGCATAAAAGCA[G/T]GCCCATAGACCAATG | 23092 |
| rs142223178 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173045 | CGTGTACGTGAGACC[A/T]GCACCCAGGTTTCTT | 23092 |
| rs142226656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939085 | CCATTCATAGCTGTG[A/G]AGCAGGAAGAAGCAA | 23092 |
| rs142234271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861306 | AGTGAAACCAATTTC[C/T]GGGAATGTTATTAGG | 23092 |
| rs142235985 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210380 | CAATCATCTCCCACC[A/G]AGTCTCTCCCACAAC | 23092 |
| rs142244436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790135 | GTTTTTGTGGGCAGA[C/G]AAACAAGTAAACAAG | 23092 |
| rs142256382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205401 | TCTGCTATATGAATC[C/T]GCCAGACCGAACACT | 23092 |
| rs142274179 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864883 | GGGATTTAAGCTGAT[A/G]TTTGCGCAGCCAATG | 23092 |
| rs142298275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930455 | GAGAAGAGTTATTCC[A/G]TCTTCTGAGTCATCT | 23092 |
| rs142303319 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995005 | CTTACACCTTATACA[A/G]AAATTAACTCCAGAT | 23092 |
| rs142303938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881956 | AGGAAGATTCTTGGG[C/T]ATTCTTATGCTAATG | 23092 |
| rs142312895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791661 | TCCTCCCTACCCCTC[G/T]CATTTAAAAGGTGTT | 23092 |
| rs142316424 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954583 | TCATCCAGCATCTCT[A/G]CACCCTCCCCTCTGG | 23092 |
| rs142316827 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:142919453 | ATTAAGCCAGCCAGT[C/T]TGTGGCACTTTGTTA | 23092 |
| rs142323545 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975450 | CTGTCTATTTTTGAT[A/T]AAAGATATTCTGTAC | 23092 |
| rs142330610 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821791 | GAAAAGCCATCTTTC[C/G]TTACAGCTTTGTTTA | 23092 |
| rs142342390 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843331 | TGTGTCTTTCTGACA[C/T]TGAGTGGAGTTCAGG | 23092 |
| rs142345602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072711 | TCTCATAGAAGTAAA[A/G]AGTAGAAGAGAATAC | 23092 |
| rs142353733 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214907 | AGCACTGTCCTTAAG[C/G]CTTTGCTCCATTAAC | 23092 |
| rs142364270 | in-del | -/TTAC | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003785 | CTCTCATAAGTATTA[-/TTAC]TTAGCTCTACTTTGC | 23092 |
| rs142383125 | in-del | -/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827916 | CTGCTTTTATTTTTT[-/T]AAATACTGTTGTTTA | 23092 |
| rs142402862 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067624 | TTCCAATTTGGTATT[A/T]TAAGTCACTATTCTT | 23092 |
| rs142404253 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956482 | CTCGGGAAGCTGAGG[C/T]GGGAGGATTGCTTGA | 23092 |
| rs142407247 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991914 | CTTGCTCTTCATGAA[G/T]ACTGTGCCAATTTAT | 23092 |
| rs142412588 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101053 | AACAAACATTGTGTC[A/C/G]CTACACTCCAGCCTG | 23092 |
| rs142423711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143069243 | TTTGATTTGTTTACT[C/T]GTTGTTTTCTTCTCC | 23092 |
| rs142430415 | in-del | -/G | 0.0463947 | 0.145069 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812535 | TAGAGGTGGGGTTTT[-/G]CCATGTTGGCCAGGC | 23092 |
| rs142439316 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991315 | AGACCTTTGGAAAAG[C/T]GCAGTATTAGGGTGG | 23092 |
| rs142460633 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949520 | AGATCAATTTTACCC[A/T]GAAGGTAGGCTGTTT | 23092 |
| rs142462235 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877051 | TATTTGGGGGTGGGG[G/T]TGTGGCAAGCAAATC | 23092 |
| rs142463726 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875897 | AGGTGTGCACCACTG[C/T]GCCTAGCTAATTTAT | 23092 |
| rs142467613 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952953 | TGACCTTGTGATCCT[A/C]CCACCTTGGCCTCCC | 23092 |
| rs142472218 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775000 | AAGGACATTTTGGTC[A/G]TTTCCAAGTTTTATC | 23092 |
| rs142479132 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093102 | CTTTTTCTAACAGAA[G/T]AGCTTTATATGTTAA | 23092 |
| rs142482271 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161272 | CCGTCTTGGCCTCCC[A/C]AAGTGCAGGGATTAC | 23092 |
| rs142487256 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796656 | AGTTCAGACGTCTTG[A/G]TAGGGCTTTCTGAGC | 23092 |
| rs142492665 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152787 | TGTAGCCTCCTTAAA[A/G]ATGACGGATTACTGG | 23092 |
| rs142522691 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041011 | CTACTGGTTGAAGAA[G/T]GGACATCAGAGGAAT | 23092 |
| rs142529043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119837 | TGATATGGTATTTCA[A/G]TAAAGGCTCAGTTTA | 23092 |
| rs142534296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868099 | AATTACCTGAACAAA[C/T]ATAAAATTGCTCTGA | 23092 |
| rs142540020 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121721 | CCTAGTCTTTCTTTC[A/G]AAGGTTTTCCTCATC | 23092 |
| rs142542059 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187184 | ACAGAGGTTAAGTTG[C/T]CCAGGGTGACACAGC | 23092 |
| rs142546098 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220887 | GGTTTCTGTTCTTGC[A/G]TCTTTCCCTACAAAC | 23092 |
| rs142546543 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020505 | GAGTGAGCTACACTT[C/G]AAAAATGGAAATTTC | 23092 |
| rs142553917 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188581 | GCTGGGTGACAATGT[C/T]GGAAGAAGGAAGAGC | 23092 |
| rs142565415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984142 | ACCTCCTGGCCTCAC[A/G]TCTGTGGTTCAGGCA | 23092 |
| rs142568008 | in-del | -/A | 0.0611083 | 0.163768 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133229 | AAAAGCCCCTCCTCC[-/A]AAAAAAAAGCTTATA | 23092 |
| rs142569655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903825 | AGAAAGATGATGTCC[A/G]CAGAATCTTGTCTAC | 23092 |
| rs142577757 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124342 | AGAGCCATGAGATGT[G/T]TTAATTTTCTATTGC | 23092 |
| rs142578569 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188121 | GCTTACACATATTTC[C/T]AGAGCCAAAAAGAAT | 23092 |
| rs142581934 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189786 | ACCAGCCTGTGTTCT[C/T]GCCCACCCTACCTTG | 23092 |
| rs142607553 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148103 | ACTAGCGCCTTTGCA[A/G]AAAGAATGTGAGGCC | 23092 |
| rs142642491 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863235 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGTGATTA | 23092 |
| rs142657452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844901 | GATTGTAGGATGGTA[A/G]CCCCCGTTTTGCAGG | 23092 |
| rs142664338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846080 | TCCATGTGTGAAAGC[C/T]ACGCATTAGTTTCAA | 23092 |
| rs142664404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216845 | AAACGTTAGTACACT[C/T]TCTCAATTGGGTTAG | 23092 |
| rs142668704 | snp | A/G | 0 | 0 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769303 | GAAGGAGGGCTGCTG[A/G]TTCCTAGACATAGAG | 23092 |
| rs142679333 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817525 | TAGAGGTGAAGGATA[A/G]GAGGGCTGTTGGTGG | 23092 |
| rs142688093 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197647 | AGGCTGCCTTTTTAC[C/T]CTTTTAATATTGTTT | 23092 |
| rs142692869 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979228 | GTTTGTCTTTTTAAT[A/G]TTTCTACTTTCTGCC | 23092 |
| rs142693672 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847329 | CTGCCTCAGCTTAGG[A/T]CACACAGCGAATACA | 23092 |
| rs142708584 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096181 | TGCTCATTTAGAAAA[C/T]ATTAGTAAACTGCGT | 23092 |
| rs142713073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218016 | TTGCAGGCCTTCTTT[A/G]TGTTCTCAAGTAAGG | 23092 |
| rs142719570 | snp | C/G/T | 0.000214419 | 0.0103521 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143134053 | CTCCAAGCCCCCGTC[C/G/T]TGCAGCGAGAGGCCC | 23092 |
| rs142733082 | in-del | -/AGATA | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172558 | TTTGAATAGCTCAAT[-/AGATA]ATATCTTCCAAAGCA | 23092 |
| rs142745125 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929185 | CTCATGGTCCGCCCA[A/C]CTCGGCCTCCCAGAG | 23092 |
| rs142747062 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856282 | TTCCTGGAGGGCCAG[G/T]TGGCAGTCGGTTGGT | 23092 |
| rs142775987 | snp | A/C | 0.0115144 | 0.0749975 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228892 | AAGAAAACAAAATTT[A/C]TGTTCAGAGGCCTCT | 23092 |
| rs142778857 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175971 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGTGTGC | 23092 |
| rs142778977 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195185 | ATCCGGACCAAGGTT[C/T]GTGCATTTGCAAGAG | 23092 |
| rs142782050 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869801 | TTGGGTTAAATTCTC[G/T]TAAATCCGGTGCAGA | 23092 |
| rs142802764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058660 | AGTCCATACTTTGCT[A/G]TGCCATTAGGGTATT | 23092 |
| rs142805079 | in-del | -/T | 0.393987 | 0.204372 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093148 | AAGCTACCTTTTTGC[-/T]TTTTTTTTTTTTGGA | 23092 |
| rs142808538 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009304 | ATCATCGTCAGCATC[A/G]TCATCGTCGTCATTG | 23092 |
| rs142812128 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938444 | ATATTAAATTGGACA[C/T]GGAAACCTTAGTTCA | 23092 |
| rs142813459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070314 | TACAAGGTCATTCTC[C/G]CCAGCCCTAACCAGA | 23092 |
| rs142815639 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140204 | CAATTTAGAGAAGTA[C/T]TGGCTTGGGAAGGTG | 23092 |
| rs142829651 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047854 | ATTATTATTCCGCTC[C/T]GTTGCCCAGGCTGGA | 23092 |
| rs142837036 | snp | C/T | 1.65059e-05 | 0.00287275 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142902039 | CATTAGCATACAGAA[C/T]GTGAGTGGGCATAGG | 23092 |
| rs142839663 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942804 | TGTTGTTTTGGAGAC[A/G]GAGTCTCACTCTGTT | 23092 |
| rs142841405 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990288 | TGTAGTTCTTGTGCC[A/G]TGGTTTTCAGCTCCA | 23092 |
| rs142843405 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890726 | GGTGACAGCAACCAC[C/T]GACATGCACGGGACA | 23092 |
| rs142845091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099223 | TTCATAGTAAATAGC[A/G]TAAGTTAAGCAAAAC | 23092 |
| rs142847256 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165015 | TTACTTCGGATTCAT[A/G]TAGAAATCCAAGAAT | 23092 |
| rs142851962 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958143 | TTTAAGTCATGTGTT[C/T]AGATAAACCATTTCC | 23092 |
| rs142858138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051740 | TCCTCTCTAATGTTA[C/T]GCAATATTCCTATGG | 23092 |
| rs142860402 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934210 | TTGTTCTCTGTCTGC[A/G]TATAATTGGTCTTCT | 23092 |
| rs142866162 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227240 | ATGTTCCCCAAGTAG[A/G]TAGCCAGCGCTGCAG | 23092 |
| rs142866899 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951028 | CTTTCCCTTTCTCTT[C/T]CCCTTTCCCTTTCCC | 23092 |
| rs142867006 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785354 | ACACCAGGATGTTCC[A/G/T]ACCTGGCACTGTTCT | 23092 |
| rs142922455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788805 | CTGGAACCAATGCCC[C/T]ACAGATACTAAGGGA | 23092 |
| rs142942884 | snp | G/T | 6.71411e-05 | 0.00579362 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207194 | TGGTTGTTATGTCTT[G/T]CAGCCCCCCGAATCC | 23092 |
| rs142942927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170633 | AGGCATTTTACATGT[A/G]TGTACTTATTTAATC | 23092 |
| rs142949893 | snp | A/T | 0.106633 | 0.204807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104422 | AGACAGAGGCAGGAG[A/T]ATCGCTTGAGCCTGG | 23092 |
| rs142954275 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024711 | CTAGATACTATTATT[A/G]ACCCCATTTACAGAT | 23092 |
| rs142961369 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954091 | GCTGTACAAATATTA[C/T]GCGTTCTAACCCCAC | 23092 |
| rs142967156 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803472 | GCTCCTGTCCTTTGT[C/T]GTTGCTAATAGAAAC | 23092 |
| rs142971904 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780628 | TTCCCTAAACTGAGA[C/G]AGCTGTACCTAGAAA | 23092 |
| rs142973666 | snp | A/G | 3.29516e-05 | 0.00405891 | synonymous-codon, intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207285 | GCCCACCTCATCCAC[A/G]TCCAGCGACTCATCC | 23092 |
| rs142976820 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910035 | ATGTGAATTAGTATA[A/T]AAAAATTTTTTGGAA | 23092 |
| rs142981356 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174237 | GGGTATGTTGTTGTA[C/T]ATCTCCACAATGGCA | 23092 |
| rs142982134 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843214 | TAGTTGGCTCTGGGA[C/T]CCAGGCATGCTCCCA | 23092 |
| rs142984669 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182717 | ATTTCCTGGCTATAA[A/G]GACAAATCCCTTGCT | 23092 |
| rs142988294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192254 | AGAAGCCTGAGGAAG[A/G]AGGTCGCATTTGAAA | 23092 |
| rs142989272 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107781 | AATGATAGTTGGTTT[C/G]CTCACCTTGGATCTC | 23092 |
| rs143000962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127817 | GGTGTTTAGAAGTCG[C/T]ATTTTATTTCTTTGA | 23092 |
| rs143003165 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206769 | TGGCCCAGAAGAAAA[A/C]AAACATGGTCATTTC | 23092 |
| rs143028179 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107068 | TGTGTTATTTGCCGT[C/T]GGAATGAAAGCAGGG | 23092 |
| rs143034710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081018 | ATATGTGTAGGGAAG[A/G]GGGATAAAGGATGAC | 23092 |
| rs143043349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003490 | ATATATGCAAACATT[G/T]AGATGCCGCATAGAT | 23092 |
| rs143046940 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893794 | TAACTGGCTTGAGAT[G/T]ATATCTCATTTTGAT | 23092 |
| rs143047239 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932334 | TTGGCCTCTCTGTCC[G/T]AAGGCATGGCTTCTG | 23092 |
| rs143054285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825636 | TATTGTAATTCCTTA[A/G]CGGGACGATACATTC | 23092 |
| rs143067646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823554 | CTCTGTTACTCTGCC[A/G]TTTGCTGGTGTTATG | 23092 |
| rs143086806 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897413 | TGTCTCTGCACATCA[C/G]CTTCTAGGCAGGTCA | 23092 |
| rs143091071 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830732 | ACAGATACACACACA[A/G]AATATGTAGCCTCTG | 23092 |
| rs143091891 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905798 | AAAAGTAATGGCTAA[A/G]ATCGCAATTGAACTC | 23092 |
| rs143094858 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784245 | CCCAGCAGGGAAGCT[C/G]TGCTCCATTGCATAG | 23092 |
| rs143112189 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204715 | CATTGTGTTCACAGA[A/G]TATGTTCCAAACTAT | 23092 |
| rs143122370 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804717 | GGCTGGTCTCAAACT[C/G]CTGACCTCAGGTGAT | 23092 |
| rs143125172 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951216 | AGGCATGTACCACCA[C/T]GCCCAGCAAATTTTT | 23092 |
| rs143126751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184558 | TCAGCTTGCTGACTG[A/G]TGGACTGGGGGAAGC | 23092 |
| rs143134743 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155509 | TTGGTTATTAGTGGT[-/G]GGTTCTTCTTTTTTA | 23092 |
| rs143135516 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168941 | TTTATTTTCATTTGG[A/C/T]TGGGTAGCATCCCTT | 23092 |
| rs143144818 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799069 | GTGTTCCACATTAAA[C/T]CTAACAGACATCGCT | 23092 |
| rs143159784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179672 | TTTCTTGGGCCTTTT[C/G]TTGTCTGAAGTAATT | 23092 |
| rs143164983 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852900 | CATGTCCTGTTGAAG[C/T]ACCATGACATTGAGC | 23092 |
| rs143166072 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149194 | GATCTGGGGGGCTTT[A/C]CTGGGGAAGGGAGGG | 23092 |
| rs143168078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187904 | TTTTGCTCTTGACAC[C/T]GATTGTCCCTTCTCA | 23092 |
| rs143169003 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889367 | CCTGTAATCCCAGCA[C/G]TTTGGTAGGCCAAGG | 23092 |
| rs143175748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816946 | GAAGAAGAGGGCTTA[C/T]GGAGAAACCTACAAG | 23092 |
| rs143181147 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173249 | AAATAAATATGGAGT[A/G]CCCTCGAACTCTTTG | 23092 |
| rs143184548 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197236 | GGGTGTATGTCTAGC[A/G]ATGGAACTACTGGGT | 23092 |
| rs143191009 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082065 | GAGTAACTCTTTCTC[C/T]GGATCTGTTGCTGGG | 23092 |
| rs143194542 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777774 | TTTGGGGGCCAGTGG[C/T]GCGGCCAGTTGTGAC | 23092 |
| rs143210841 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067978 | AGACCAGCCTGGCCA[A/G]CATGGTGAAACCCCA | 23092 |
| rs143219468 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225729 | CCCTCCCTAGCTTCC[A/G]TGTGTCTGTGCAGTG | 23092 |
| rs143220966 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086339 | GGAAATAAACTTGGG[A/C]CTCCATCTTTATTTT | 23092 |
| rs143222099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154411 | CATGAAAATTAAGAT[C/T]ATCTTTTACTTACGT | 23092 |
| rs143233610 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986862 | CTGTTCAATTGGTCT[C/G]TATCTCTGTTTTGGT | 23092 |
| rs143241383 | in-del | -/T | 0.0360663 | 0.129354 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185456 | ATGGGGCATCCCTCC[-/T]TTTTTTTCTTTTACC | 23092 |
| rs143255783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869149 | CAAGTTCTAACCTCA[A/G]TGATGGCCTTTCTGA | 23092 |
| rs143259264 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922356 | TTGTGTATGTATTAG[C/T]AACTATTAGAAGGTC | 23092 |
| rs143261813 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798551 | CTCAAATGGAGTATT[G/T]TGTAGCATTTTAGGA | 23092 |
| rs143263644 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971036 | TCTACAAATTTTTTA[C/G]GTGGCATTGGAGGTT | 23092 |
| rs143264971 | snp | C/T | 0.121369 | 0.214369 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022230 | GTGCCTGCTACCACA[C/T]CTGGCTAATTTTTTT | 23092 |
| rs143277806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150445 | GAGTGCACACACTAG[A/G]TCGAAGTAGTGGAAA | 23092 |
| rs143283855 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034501 | CTAGACATAAAAGAC[C/G]GCATCGTGTATGATT | 23092 |
| rs143284951 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870574 | AGTTATTCATGCTTA[A/C]CTTTCCTGGTTCCTC | 23092 |
| rs143285870 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083115 | AGCTAGAGCTGGAGA[A/C]TTTTTCTTCGTCTTC | 23092 |
| rs143293441 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801078 | TCTTGAGGCATCTTT[A/C]ACTGCATGATGGTGG | 23092 |
| rs143293956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880849 | AAGATGATGTTTAGT[C/T]AGGGTCTTTCAGAGG | 23092 |
| rs143298610 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809722 | CCAGTCCTGCTGGAG[C/T]CATCCACTCCTTCAT | 23092 |
| rs143301561 | in-del | -/TTGA | 0.491732 | 0.0637633 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007820 | TGGCTATTTTTATGT[-/TTGA]TTGCTGTTTTAAAAA | 23092 |
| rs143306137 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189739 | ATCAGATATTTAAAA[A/T]GCCAATAGGAGCTTT | 23092 |
| rs143315910 | in-del | -/AGAG | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968212 | TGGAAACTGAGACAC[-/AGAG]AGATTAAGTATTTTA | 23092 |
| rs143316029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209564 | GGTGGGGAGATCACC[C/T]GAGGTGAGGAGTTCA | 23092 |
| rs143324784 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967924 | AGCTTCTGGAGAGGT[A/G]GTCCTTGCTACTATT | 23092 |
| rs143333376 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049907 | TTTCTTCTACGGCTC[G/T]CCTTCTGATTCACTT | 23092 |
| rs143348422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112612 | TAAACAAAAGCTCCC[A/G]ATTCCCCTTTCATCT | 23092 |
| rs143350579 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038359 | CAAAACAGTTGTAAT[G/T]TATGGAAACATTTTT | 23092 |
| rs143356277 | in-del | -/T | 0.0275645 | 0.114116 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784418 | CTTGGGATTTTGTGC[-/T]TGAAACCGTACGTAA | 23092 |
| rs143361733 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864563 | TTTAGTAGTTCACAA[C/G]AATGGGGTTGATCTG | 23092 |
| rs143365270 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040247 | AGGGACTCCTAGTCC[G/T]TGAATCATGCAGAAT | 23092 |
| rs143367829 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838214 | AGTGAGCTGAGATCC[C/T]ACCACTGCACTCCAG | 23092 |
| rs143371264 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969520 | CTTGATTTTATGTTG[G/T]CCTGTTCTTTAGAGA | 23092 |
| rs143382612 | snp | A/G | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225249 | CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCACT | 23092 |
| rs143396280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165679 | CCCAATAATGAACGT[C/T]GTACCCAATGGGTAA | 23092 |
| rs143409293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043482 | TTTCCAGTTTGGGGC[A/G]ATTATGATAAAGCTT | 23092 |
| rs143414658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974275 | TGAAACTTTTCTCGA[C/G]CTACCTGGTTACGAT | 23092 |
| rs143414760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925596 | TCATTTTCCCAGTAG[C/T]ACTTTAGAAACAAAG | 23092 |
| rs143416313 | in-del | -/TGAG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858092 | TGTGTGTGTGTGTGT[-/TGAG]GTGAGAGAGAGAGAG | 23092 |
| rs143432162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129803 | ATGCCTACTCTTTGC[C/T]ACATACTGCACTGAG | 23092 |
| rs143432470 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169772 | GAGAAGAGACAGCCA[C/G]AGATGTCACTACACT | 23092 |
| rs143432663 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177519 | TACATGTATTTGATA[C/T]GCATGCTCACCCATA | 23092 |
| rs143441289 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084522 | AGATTTGGAGGGAGG[C/T]GTGTTTTTAACCAAA | 23092 |
| rs143446689 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059818 | TCAAGAAATCTACCT[G/T]TAGACAAGCTCTCAT | 23092 |
| rs143451054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141612 | TTGCTGTGAGTCATG[A/G]TATAAAAGTAGGTGT | 23092 |
| rs143460300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970123 | TAAAGTGTTTGTTGA[A/G]CATGAGAGTTGGTTG | 23092 |
| rs143513726 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889993 | ATACAAAATTGGCCG[A/G]GCATGGTGGTGCATG | 23092 |
| rs143515205 | in-del | -/TT | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861777 | GGAGGCAGGTTTCCC[-/TT]TTTAGTGCCTTTTCA | 23092 |
| rs143525315 | in-del | -/C | 0.118584 | 0.212673 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849925 | CAGTTAGTCCCCAAA[-/C]CCCACGGGTGTTCTT | 23092 |
| rs143537406 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821637 | CATCTGGTAGCTGCA[A/G]AATTGGAACTGGCAT | 23092 |
| rs143546669 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785098 | ACCATGCCCGGCTAA[G/T]TTTTTGTATTTTTAG | 23092 |
| rs143551103 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911714 | TCCCTATTCCCTCCC[A/G]TTTCTCTGGGACACC | 23092 |
| rs143551504 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136511 | CAAGTCTGTGTGTTC[G/T]TTAACTGCAATTTAT | 23092 |
| rs143552927 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167819 | AATGTGCAAAGAGAA[A/G]CTGACAAGAGATAGT | 23092 |
| rs143553624 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852606 | CTCACATGCATTCTC[A/G]CATGTTGATGCATTT | 23092 |
| rs143553838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221523 | GACAAGAAGCTGGAT[G/T]GATTGATTGAGACAG | 23092 |
| rs143559074 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227036 | CACAGTTGAGGGGGA[A/G]AAAGACAGAAAGAAG | 23092 |
| rs143561845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778682 | TGCAGTGATTATTTG[C/T]ACACCTGCTTTTGTG | 23092 |
| rs143583279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955440 | GATGGGCCTAGAGGA[C/G]TGAATAGGAAAATTA | 23092 |
| rs143583768 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836164 | GTTTAATTCTGGGTC[C/T]AGGCATCCTGGGCAG | 23092 |
| rs143584443 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927423 | GGAGTCACACAGTCA[C/T]ATAATCTTTTGTGTC | 23092 |
| rs143591652 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225117 | AGGGGATGTGCATTC[A/G]CATACTATTACGCTT | 23092 |
| rs143591758 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855612 | TATGTACTAGACACT[A/G]TTCCTTCCTTCTATC | 23092 |
| rs143606476 | snp | A/G | 1.67248e-05 | 0.00289173 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222404 | GGGGACTCTGAACGG[A/G]AAGACTGGCCTCATC | 23092 |
| rs143609737 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813206 | TTGGCCTCCCAGAGT[A/G]CGGGGATTACAGGCG | 23092 |
| rs143611483 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194716 | ATTTGTTTTTATTCA[C/T]AGATGGTGAAACTCT | 23092 |
| rs143615415 | snp | A/C | 0.030278 | 0.119257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061327 | TCATGGTAATTTCCT[A/C]ATGTTTACATATTAT | 23092 |
| rs143636904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120762 | GTTCTAGGCAAAATG[A/G]AAATGATAAAGCGTG | 23092 |
| rs143646283 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017652 | TTTATTTCTTACTTT[G/T]TGCCCTCATCATTGT | 23092 |
| rs143654517 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945164 | TACCCCATCCCATCT[C/T]AAGGAGCCACAGGAG | 23092 |
| rs143667168 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969049 | TGATCCTCCTGCCTC[A/T]GCCTCCCAATTAGCT | 23092 |
| rs143674357 | snp | A/C | 0.0053932 | 0.051648 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902050 | AGAACGTGAGTGGGC[A/C]TAGGGACAGGCTTCT | 23092 |
| rs143675124 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891020 | TCCCCCTCCACTTGC[A/T]GTGTCAGTTGGCAAG | 23092 |
| rs143675987 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902853 | CGAGATTGACATGCA[C/G]TGGGCTTACTGGAGG | 23092 |
| rs143679460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834956 | AAGTTTATTGTTAAT[A/G]CAGAGCTCTATAATA | 23092 |
| rs143681862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133386 | TTTATCAAGATAAAC[A/G]AGGAAAAGCTCAGCA | 23092 |
| rs143694586 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015834 | TGGGATAAATCCCAA[C/T]AGATTTGAAGGACAA | 23092 |
| rs143695106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883846 | TGATTATTTGTTTAC[C/T]GGTTAATCATGGTTC | 23092 |
| rs143696512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063451 | TAAAAAAACTTCAAA[A/G]GCAGCTTCCCCATTG | 23092 |
| rs143714757 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853586 | CCTTTTGTAAAAGGG[A/G]TTTAAACAATAGTAT | 23092 |
| rs143715353 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846313 | GCTCAGAGGGGTGCC[A/G]AGGTATATGTGTCGG | 23092 |
| rs143715674 | in-del | -/A | 0.0807149 | 0.183963 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083056 | CAAGAATCTCAGCCG[-/A]GTATAATACAGCAGT | 23092 |
| rs143717344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217221 | GAAAGTCTGTTGTTT[C/T]GTAATGATTAATCTT | 23092 |
| rs143721289 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769670 | GTGTAGCGAAGGATG[A/G]CAGGCAGTAGACTGT | 23092 |
| rs143724428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158126 | TGCTCTCAGACTGCT[C/T]CCCCTACCAATGAAC | 23092 |
| rs143733700 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018525 | CCACTGTATGAGATG[A/T]TCCATGAAGATCCAT | 23092 |
| rs143734303 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061889 | AGTCCCTTTTTAAGG[G/T]CTAGGATGATACTTT | 23092 |
| rs143735069 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132012 | CTGCTCGGGAAGTTA[C/G]GAGTTTTTTCTTGCT | 23092 |
| rs143747741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181989 | GGCTTGTACGCTCCT[C/G]TGCTTATTCTTGTCC | 23092 |
| rs143750962 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142907743 | AGCACTACTGTACAT[A/G]TCAACGGGATTCCAA | 23092 |
| rs143756806 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089316 | TGTGACACAGCACCC[A/G]ACAAGAATAAGTACA | 23092 |
| rs143758866 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013968 | GGAGCCAGAAATTAC[C/G]TTCCACTTCATGGTG | 23092 |
| rs143765674 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079931 | CCCTCTTTAAAAGAC[C/T]AAGCCAGCTGTCACA | 23092 |
| rs143771529 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000368 | TACAGACAGGGAACC[A/C]CCTAGGTGTCCATCA | 23092 |
| rs143773080 | snp | C/T | 1.67072e-05 | 0.00289021 | missense, upstream-variant-2KB, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770834 | GAGACGCTCAAGTCG[C/T]ACGAAGCAGAGCTGG | 23092 |
| rs143780679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975967 | TAAACCACCGTATGG[A/G]GGAAAAACTCTCCGT | 23092 |
| rs143784204 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896574 | CTCCTTCTTCTCCTT[C/T]TTTTGTCTCTCCTCC | 23092 |
| rs143796300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838932 | TGGTCTTTTTATGCC[A/G]TCATGACTTATTTGG | 23092 |
| rs143818085 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210040 | TAAATATTGAATTAG[A/T]TCTAATCAGTGGTCC | 23092 |
| rs143826002 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024409 | TCAGTGATGTGGGCT[C/G]TGTACTGACAGCAGG | 23092 |
| rs143837873 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213895 | ACTTCCCACGAGAGG[A/G]GACTAGGTAGCTTAC | 23092 |
| rs143838874 | in-del | -/TTTTC | 0.282895 | 0.247826 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993818 | GCCCAGCTAATTTCT[-/TTTTC]TTTTCTTTTCTTTTC | 23092 |
| rs143843685 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904673 | TGATGGGGCCGTGCC[A/G]TTTAGGATAGCACAT | 23092 |
| rs143848083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154201 | TCATGGATTTTATAT[C/T]CTAGTGGAGACAGGA | 23092 |
| rs143850414 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113234 | AAGACAAATCCTTTT[C/T]CCTTTTCTCTAAACA | 23092 |
| rs143850911 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156595 | ATTCTGATACATGCT[C/T]AAGTCTGAGAGCCAT | 23092 |
| rs143851317 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065951 | GTTAGTGCTTGAACC[A/C]GGTGGGGTCTAGCTT | 23092 |
| rs143860114 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987897 | GCTGGATTCGGTTTG[C/G]CAGTATTTTATTGAG | 23092 |
| rs143872535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881974 | TCTTATGCTAATGTG[C/T]TACTCTGGAGTAGGG | 23092 |
| rs143880412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943250 | GGCATGACTTCCTAT[C/T]TGAGACTGGTTCCTG | 23092 |
| rs143907745 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873115 | TCCTTTGGCAAGTGG[A/T]TTCCCACATGTCAAA | 23092 |
| rs143909975 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832180 | GAGTGAAGTGTTATC[A/T]GTTTCCCTCTAATAA | 23092 |
| rs143917831 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921820 | AGGTGGAACACACTA[A/G]TATTCCCCTCTGATG | 23092 |
| rs143927631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835314 | GATAGAATTTATGGT[A/G]TAGAGATGTCTTCTT | 23092 |
| rs143937347 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207732 | GGCTCTCTCAATTTC[A/G]TGTGCTCTCTGCACT | 23092 |
| rs143943050 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886446 | AATAAGTATTTAATC[C/T]AGTTTTTAGAGTAGT | 23092 |
| rs143949424 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201902 | ATTTAAAAAATCACA[C/G]AAGTGAAGAGTGCTG | 23092 |
| rs143955743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841338 | AGGAGGTGGCCACAG[A/G]TTTCAAGTCTCACGG | 23092 |
| rs143964388 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191429 | CACACTTTTACAAGA[G/T]GGTATAAAAGGATTA | 23092 |
| rs143967480 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100032 | AGACAATTTGCCAGA[A/G]TGCAGTCCAGGGAAA | 23092 |
| rs143973142 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211271 | TTTTTTCATATATGT[A/G]TGTCCCATGCAATAT | 23092 |
| rs143985990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152314 | AATAATTAAGGAAAC[G/T]CAGAATGTAGAAATA | 23092 |
| rs143995745 | snp | C/T | 0.00114273 | 0.0238759 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216182 | CAAGTCCTTTTTTTC[C/T]CCAGCAGAGTGTCCT | 23092 |
| rs144018050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053108 | TGTCGGACTTTCAGG[C/T]TCTGTGTGGTGGCAC | 23092 |
| rs144028504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947263 | CCAAACTAAGGAAAT[C/T]ATCAACATTCTTGGG | 23092 |
| rs144030666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874736 | TGGGTTCTGACGCAA[C/T]GCCATGACAAAGGTT | 23092 |
| rs144035316 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004474 | AACCCCAAATGCAGC[A/G]AAATTAATCAGCCCA | 23092 |
| rs144049219 | in-del | -/CT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832392 | ACAACCGAGAGCAGG[-/CT]CTCTCTCTCTCTCTG | 23092 |
| rs144050915 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837717 | TCTTGTTCCTTTTTG[A/G]GCATCATGGTTTATG | 23092 |
| rs144050972 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878910 | GTCTTGGTAGAGCAA[C/T]ACAAAATCAAGCTTG | 23092 |
| rs144057466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042515 | ATGAGTCCATGAGCC[A/G]AATTTGCTTAGGCTG | 23092 |
| rs144058530 | in-del | -/AAAAAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004018 | AACAAATTTATAGAC[-/AAAAAAA]AAAAAAAAAAAAAAG | 23092 |
| rs144064733 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938955 | TAGGTGGAATTAGAT[G/T]AAGAAGGTAAGAAAC | 23092 |
| rs144069758 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839901 | GAGAGAGAGGAGGGG[A/G]GGGGAGGGGAGGGGA | 23092 |
| rs144079246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839988 | CTTTTGGTTGAGGCA[A/G]TTGCAGTGGTCCAGC | 23092 |
| rs144081300 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210367 | GTCCCCAGTGATTCA[A/G]TCATCTCCCACCGAG | 23092 |
| rs144095965 | in-del | -/C | 0.312348 | 0.242101 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040589 | TAATCAAATAACAAA[-/C]ATAATTTCAGATATT | 23092 |
| rs144096451 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000794 | AAAAAACCAAATACT[A/G]CATGTTCTCACTCAT | 23092 |
| rs144097046 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002011 | TCTGTGTTGGATAAC[A/G]TAACATTCACCTTCT | 23092 |
| rs144114022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929844 | CTGGTGAGCCACTAG[C/T]AGGAAACGAACTAGA | 23092 |
| rs144115538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964214 | TGAGGAGATGAAGAC[A/G]TAAAAAAGATAAGCA | 23092 |
| rs144116660 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007045 | TGAAACCCCATCTCT[A/G]CTAAAATACAAAAAA | 23092 |
| rs144117286 | in-del | -/GTATATATGT | 0.494855 | 0.0504572 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963164 | GTGTAGTATTCCATG[-/GTATATATGT]ATATATATATATATA | 23092 |
| rs144146598 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877922 | GTGGAGAAGACTTCA[G/T]TGAACCAATTAAGTA | 23092 |
| rs144172530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118498 | CGGGCAGGCCAGGCA[C/T]AGTGGCTCACGCCTA | 23092 |
| rs144172767 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184242 | CTTCCTGCCCATTAG[C/G/T]GGGTAGAGAATGCCT | 23092 |
| rs144179779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821128 | TTCTGTTTTTATTTT[C/G]CTTTTATTATCCCCT | 23092 |
| rs144183147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162352 | TTGATCCTTTGCGTG[G/T]AAGTAGAATTAGAGG | 23092 |
| rs144187973 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199110 | CCGAACTCTGTCATT[G/T]TTTAAATAAAAATGC | 23092 |
| rs144202759 | in-del | -/TA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928247 | TTTTTTTTTTTTTTT[-/TA]TAAAACTCATTGCCT | 23092 |
| rs144237918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042712 | GGGACAGTTCTTGTG[C/T]TAGTATTTGTAATTT | 23092 |
| rs144240558 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980211 | CTGTGAGACTCATCC[A/G]TGTTTCCATGTAGCA | 23092 |
| rs144242497 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121379 | GGTGGTGGCAGTGGT[-/G]GGGTAAAATTGATTG | 23092 |
| rs144246044 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971878 | TTCCTATGTGATACA[C/T]GGAGTTTAAGATACA | 23092 |
| rs144246533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899892 | GGAGCACTTGCGGGT[A/G]TGCCCAGGTGGCATC | 23092 |
| rs144261200 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088243 | TGATTAATGTTCATC[A/G]TTTACACTAAACTGT | 23092 |
| rs144265200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013322 | TGATTTTGCCTCTTG[A/G]CCCACAAAGCATAAA | 23092 |
| rs144267731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862590 | CTGGTAGAAGTGGTG[A/G]TACTCAGATTTCTAA | 23092 |
| rs144270958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790682 | CTCACTGTGTTTAAG[C/T]TTGGCTGACCTCAGA | 23092 |
| rs144276326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857951 | AGAATTTCTGATCCC[A/G]TAAGTCTGGGGCAGT | 23092 |
| rs144285952 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148003 | GAAACTAGGTCTACT[C/T]TGCTAGGATCAGAAA | 23092 |
| rs144299188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811476 | CAATCCTGGCCTGTC[C/T]GTCACGTGTAGTTGG | 23092 |
| rs144300118 | in-del | -/TGTGTGTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796085 | GTGTGTGTGTGTGTG[-/TGTGTGTT]ACGTCTCTCCTACTA | 23092 |
| rs144314712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815831 | ACCAGGTCTCACTCT[A/G]TCACCCAGGTTGGAG | 23092 |
| rs144350586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130080 | GATGGTGAGGTCCGT[A/G]TAGCTGTAGGTGTTG | 23092 |
| rs144369486 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929923 | CTCTAGGGCAGGGGG[A/T]ACAGGAAGGAAAAGA | 23092 |
| rs144373356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856910 | TACCATGAACTGGGT[A/G]GCATAAAACAACAGA | 23092 |
| rs144374308 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125374 | TAGAAACACCCTCTC[A/C]CCCCAACCCAGAGAA | 23092 |
| rs144383874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143502 | TACTCATGTTTTTCC[A/G]TTCCTGATTTGTACA | 23092 |
| rs144392671 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060683 | ATGTGCCTCAAAGCA[C/T]GGTTAGAATAACCCG | 23092 |
| rs144393507 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815069 | GGGGTGGCATGATCT[C/T]GGCTCACTGCAACCT | 23092 |
| rs144412491 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143861 | TTTGTCACTCCTTAT[A/G]GAACATATGTTTGTG | 23092 |
| rs144412690 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029594 | TTAACCTTTTTGTAG[A/T]GATGAGGTTTCACCA | 23092 |
| rs144420990 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187975 | AATGGAAAATGAGAG[C/T]ATTCCATCTCACAGG | 23092 |
| rs144431765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019556 | TTGTAATGAGTCCAG[A/G]TTGGAAGCAGGATGA | 23092 |
| rs144432823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946679 | TAGAAAGTCTGCAAA[G/T]TAGGTTGTTTGCTTT | 23092 |
| rs144434066 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065722 | TCCTGCAAGTGCAGC[C/T]TGGTAGCCTGGAGCC | 23092 |
| rs144434279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944224 | TAGAAATAAACCCTT[C/T]TGTTGTGTAGCATTT | 23092 |
| rs144444543 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870890 | AAGTGGAGAAGGGAG[G/T]TTCTCCAAAACAAGC | 23092 |
| rs144445944 | in-del | -/AC/ACAC/ACACAC/ACACACACAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955095 | TAGTGAGACCTGTCT[-/AC/ACAC/ACACAC/ACACACACAC]ACACACACACACACA | 23092 |
| rs144452311 | snp | A/C/T | 8.25179e-05 | 0.00642288 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142903608 | GATGAAGGAGAATCC[A/C/T]CTTGAGCACAAGACC | 23092 |
| rs144462684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101787 | CTGCTGCATGTTCTA[C/T]ACAAAATTTAACTGG | 23092 |
| rs144469783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961008 | CTTGCCTCTTCCCCA[C/T]CTCTAGAAGCTTCTA | 23092 |
| rs144476329 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885795 | GAAATGTTAGCATCT[C/T]AAACACTTTGGTTAT | 23092 |
| rs144485418 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229146 | GTGCTTATTTCTGAT[G/T]AGCTCTGAGAAGCTT | 23092 |
| rs144490130 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983318 | TTCAAGCGACCCTCC[C/T]GCCTCAGCCTTGTGA | 23092 |
| rs144494244 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863342 | TTGAACTCCTGACCT[C/T]GTGATCCGCCCACCT | 23092 |
| rs144494416 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170354 | CAGTGGGGCAGCCAG[C/G]ATCCACCTCACGAGC | 23092 |
| rs144495770 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848771 | AGTCTACAAAATTGG[A/T]AGTTCCTTAAGACAG | 23092 |
| rs144507711 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218587 | AGTTGTGTACACAGG[C/G]ATGTATGGTGTACAT | 23092 |
| rs144517387 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065217 | TTAGATTTCTTATAC[A/G]TTGGCCTTGGGAGCG | 23092 |
| rs144527723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183669 | TGGAAATTCCCCCGG[A/G]GCCTCCTCGGACGCC | 23092 |
| rs144534067 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867397 | TACAAGGGACTGTAA[C/T]TTGCTTTTCTTATAA | 23092 |
| rs144536333 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015345 | GTATGGTAGCTCATA[A/G]TAAGGTCAGAGGAGC | 23092 |
| rs144554815 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978894 | TTACCACATTTATTT[C/T]TGAAAAAGGAATTAA | 23092 |
| rs144562958 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898768 | GAGTTAAAGGGAGTT[A/G]TGTGGCTTAGCCCCC | 23092 |
| rs144571196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803888 | ATCACTGAGGAGTGT[A/G]TAGTTCCAGAGAGGG | 23092 |
| rs144577747 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145400 | GTTGAAGCCCAGGGA[A/G]CCGTCCTCACTCTCT | 23092 |
| rs144605351 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143756 | GGCTAATGGTGACCT[C/G]ACCTGCCACGTTAAT | 23092 |
| rs144610019 | in-del | -/CTGAGTAA | 0.307176 | 0.243374 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039330 | TCCTACCTCAGCCTC[-/CTGAGTAA]CTGAGTAACTGGCAT | 23092 |
| rs144612629 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844603 | GGCGTAGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 23092 |
| rs144615470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077236 | AAAAGAGTGGAGCAG[A/G]TTAGCTAAGCTACAG | 23092 |
| rs144619495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142959999 | AAGGGCCCAGTAATA[A/G]AAATGGCCTCTAGGC | 23092 |
| rs144634163 | in-del | -/GTGCCTATC | 0.0322114 | 0.122752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826764 | AGTCTGCTGTCCTCT[-/GTGCCTATC]TCCACCAAGCCCTCC | 23092 |
| rs144637865 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129205 | TGCAAAGAACAGTAA[C/T]TATATTTACACTTAT | 23092 |
| rs144648262 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030138 | TTTCTGAATACTGAA[A/G]GTTGGAGTTGAGCAA | 23092 |
| rs144655258 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207611 | GCATGAATCAGCATG[C/G]CATTTTTCACACCCT | 23092 |
| rs144661167 | snp | C/T | 0.00256747 | 0.0357372 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142879388 | GATTGAGAATGCCAG[C/T]GAGGTGCTCATCACT | 23092 |
| rs144661932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178439 | AACTTTGCAAGAAAC[A/G]TAGAAAGATGGGAGA | 23092 |
| rs144667066 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046872 | GAAAATAACAGTTCT[A/G]TATACTAGAGTTAAC | 23092 |
| rs144678476 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070998 | GGGACCACAAAAGAC[C/T]GTGAATAGCAAAAGC | 23092 |
| rs144687412 | snp | A/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005053 | ACTCTAGAGTTCCCT[A/G/T]TAAAGCACAAGTAGG | 23092 |
| rs144700557 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181910 | TCTCATGGTCTACAT[A/G]GTCAGCCATTGTTTA | 23092 |
| rs144700671 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142432 | AGCATGAGCCACTGC[A/G]CCCGGCCTACTTTTC | 23092 |
| rs144715502 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825913 | GTGCTGTGTGCTGGC[G/T]TGGGAATTGTGGAAT | 23092 |
| rs144719736 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185662 | TCAGCAAGTATCAAT[C/T]CTTGCCATTCTGTCA | 23092 |
| rs144727299 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113787 | GAAGTGAATGAGGGA[G/T]AGGCCCTCTTTTTCC | 23092 |
| rs144766330 | in-del | -/AAAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158881 | TTATTGTCCACAAAC[-/AAAC]AAACAAACAAAGGCA | 23092 |
| rs144775639 | in-del | -/ACAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162284 | CCCAAACACACACAT[-/ACAC]ACACACACACACACA | 23092 |
| rs144778569 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808415 | AGTAATTTCTGCATT[C/T]CCTTTTCTTTCCTTT | 23092 |
| rs144793233 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221770 | TAAAGCAATTCACCT[G/T]CCTCAGCCTCCCAAG | 23092 |
| rs144797020 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188712 | CTGAAGGGAACTGAA[A/T]GAGCTTGTACCACTG | 23092 |
| rs144818872 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890569 | AAGGAAGATATTCTG[A/G]CTCCTGTGTGCAGAG | 23092 |
| rs144826844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810093 | GCCCTGCAACCTGAT[A/C]ATCTCCAACAGGGAA | 23092 |
| rs144829132 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793712 | TGTGCCTCAGCTTCT[C/T]GAGTAGCTGGGATTA | 23092 |
| rs144833017 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036290 | CTTAAAGATTATCAC[C/T]GGGTAACCAAAACAT | 23092 |
| rs144834118 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191698 | ATGACTGAGTTTGGG[C/T]GCCACCACCCAGTAG | 23092 |
| rs144836258 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108574 | TTCAACTTCAGCCTC[C/T]CAGTGTTTTTTCAGA | 23092 |
| rs144842330 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127395 | TTTTGATGCCTATTA[A/G]TGTTTGACAAAATAA | 23092 |
| rs144843586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779758 | TGAGTTGAACTTTGG[C/T]TGTTTCTGTGCCAAG | 23092 |
| rs144849107 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965178 | AAGGCAGAGCCAGGT[A/G]TACAGGATGGAACAT | 23092 |
| rs144855613 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847584 | CTGGTCTCAAACTCC[A/G]GACCTCAGGTGATCC | 23092 |
| rs144855854 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143069987 | CATGTCTTCAGATGT[A/C]CCCTGGGCCCAGAAT | 23092 |
| rs144864749 | in-del | -/CA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162294 | CACATACACACACAC[-/CA]ACACACACACACACA | 23092 |
| rs144866190 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994242 | GAAGGATGTTCACGG[G/T]CAGAGATGCATAGAA | 23092 |
| rs144877352 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088089 | CACATAAAGCTGGTG[C/G]TACTGTTCCTCACGG | 23092 |
| rs144885487 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943077 | GAGCCACTGCACCTG[-/T]TCCTGGATTGTGATC | 23092 |
| rs144886894 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920426 | AATTTCTCACAGATG[C/T]AAGTGACACGTGGAT | 23092 |
| rs144891140 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851532 | ATGAACAGCTTGGCA[C/T]TTTGCCCCTCATAGG | 23092 |
| rs144895876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044452 | ACCATGTTGGCAGAA[A/G]GCTCCAGCGAGGACT | 23092 |
| rs144896264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963000 | GTTGTTCCCCTCTGC[A/G]TTCATGAGTTCTCAT | 23092 |
| rs144896339 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913615 | ATCTCCAGGAGATTG[A/C]GTAGTAGACTTTTAA | 23092 |
| rs144901276 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220911 | TACAAACTGAAACTA[A/G]AATTCTGTAGCAGTG | 23092 |
| rs144921528 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864328 | ATAGCACTGTTTCCC[C/T]GGTGCATTTAAAAGG | 23092 |
| rs144932873 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918302 | CAGGCATGCACCACC[C/T]CGTCTGGCTAATTTT | 23092 |
| rs144939960 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149660 | ACAATCACCTGAGAC[A/G]ACTTGGGTCTCAGCC | 23092 |
| rs144940451 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046644 | CTGTGTGTCTGGGGG[-/T]TTTCCCCCCTGAATA | 23092 |
| rs144946744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849783 | GTGCCTCAATCCTGC[C/T]GTGTTTCTGTCCTCT | 23092 |
| rs144951995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128351 | TCTGGAGATATGGAA[A/G]ATCACAGCTCTCCAT | 23092 |
| rs144959128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220167 | ATAAAGCGGGAGGGC[C/G]TGGTTTTTGTTTTTT | 23092 |
| rs144973531 | snp | C/T | 6.66856e-05 | 0.00577394 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057597 | AACCTTAAAGTTGTT[C/T]AGCTGTGACACTGAT | 23092 |
| rs144980456 | snp | A/G/T | 0.000164724 | 0.00907396 | missense, intron-variant, synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207304 | AGCGACTCATCCCCC[A/G/T]TCAGGTCTGTTGCAG | 23092 |
| rs144996605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816771 | GGCAAGTCATTTGGG[C/G]TTGGTTCGGAGGAAA | 23092 |
| rs145001608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040011 | GTGTGTATGTGCATA[C/T]GTATTTATGGTGATC | 23092 |
| rs145005019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127133 | TTAAGAAGGACAACC[A/G]TATCAAGAAAACAAA | 23092 |
| rs145011750 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014598 | TCTTGTGGGAGGAAA[C/G]AATGGAGATGAATTC | 23092 |
| rs145014916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008427 | AGATGAGATGATATT[C/T]GATGGTGTAGAACCA | 23092 |
| rs145016370 | snp | A/G | 0.0123927 | 0.0777351 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054404 | TTAGTTCCATTTTAT[A/G]CTGTGCTTTATGTAT | 23092 |
| rs145017685 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941159 | TCGAATGGTAGTTCT[A/G]TTTTAAGTTCTTTGA | 23092 |
| rs145019936 | in-del | -/AAAG | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131404 | AACTCATTAGAAAAA[-/AAAG]AGACAAAATTTGGAG | 23092 |
| rs145043022 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858821 | GTGGATAGGGAATGC[G/T]AGGAGACTGCTTCCC | 23092 |
| rs145048479 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776944 | TGTTGTCTTTCTTTT[C/T]GATTGTAGCCACTCT | 23092 |
| rs145049642 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162214 | AGACCTCATGGTAGC[A/G]TGGTAGGAGCTCCAT | 23092 |
| rs145052990 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832959 | AAAGAAGTGAAAACT[A/G]CCTGTATCTGTAGAA | 23092 |
| rs145054435 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220785 | CTTTTCCTAAGGAGG[C/G]ACTCAAGGTGTACCC | 23092 |
| rs145057152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012167 | AGTACAGAAACCTGT[C/T]CTCTTTATACTCATC | 23092 |
| rs145070942 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124207 | TATAAGGTATTTACT[G/T]TGTGCTTCGGAATAA | 23092 |
| rs145074095 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223083 | ATGCACGGGAACACA[A/C]ACACCCTGCGTTTCT | 23092 |
| rs145080688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049055 | TCCATATAATGAGTC[A/G]TCTTACCCCTTTCCA | 23092 |
| rs145081423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051744 | CTCTAATGTTACGCA[A/G]TATTCCTATGGTTAC | 23092 |
| rs145108078 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106692 | TGGTCAGGCTGCTCT[C/T]GAACTCCTGACCTCA | 23092 |
| rs145120354 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032003 | TCTGTGGTTTTCCCT[A/G]AGATTCTTCAAGGTT | 23092 |
| rs145127944 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773227 | TTTATTATATCTATA[A/T]ACAGAAGTGTTTTCC | 23092 |
| rs145135401 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793545 | GACAGTGAAGGCAGT[A/G]CTAGTTATCACCATT | 23092 |
| rs145136305 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017227 | AGCAGTTAACAAAAG[A/G]GAATTTCTGAATTCG | 23092 |
| rs145142531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897500 | ATGAGATCAGTGATT[C/G]TCAGTGTTAGACATG | 23092 |
| rs145161350 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022077 | CCCTGATTTTATTTT[A/G]TTTTATTTCATTTAT | 23092 |
| rs145162945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901485 | ACTTCCTTTTCTGCC[C/T]TCCTCTTCTGTGTAA | 23092 |
| rs145167309 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834528 | CAATAGTGTTTATTT[A/C]TTGTGACTCAGTGGA | 23092 |
| rs145172749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123008 | ACCTCTTCAAGCATG[C/T]GTGCTTCAGGAAAGC | 23092 |
| rs145175667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950170 | TTTTAGGTATGGGTA[A/G]GGTGTGTGTGTCTGT | 23092 |
| rs145182236 | in-del | -/AAG | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824719 | GTCTCTGTGGGACTT[-/AAG]AACATATAGGGAATG | 23092 |
| rs145183801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918615 | TCACATCTCCTCTAA[C/T]TTCTTTTCTCTAGTG | 23092 |
| rs145189705 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850701 | TAGTAGGTCCTCTAT[G/T]AGTCCTATTTCTACC | 23092 |
| rs145192320 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791555 | CTAGAAGAAATGGAC[A/T]GATGGCTGACTCTTA | 23092 |
| rs145200035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208357 | TTGGGCTTTGGGAGT[A/G]TTTTCCCTTCTGTCT | 23092 |
| rs145200107 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172677 | CTGAAGTATTGAAAG[A/G]TTGTTTTTACTATGG | 23092 |
| rs145210336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809537 | AGGCAGTGAGTCCCG[C/G]TGGTTCAGGGGCCAA | 23092 |
| rs145216282 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906887 | CAATTTTTTTTTTTT[-/T]AACAATTTCTGCTGT | 23092 |
| rs145223638 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111880 | CAACCACGTCCCCCA[A/C]CTGCCCCCAGCTTGG | 23092 |
| rs145225872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037979 | AAGATCAAGGAGGCT[A/G]GTTCATCCTGATGGT | 23092 |
| rs145234539 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172349 | GAGAATAAAAAATAA[A/G]ATTAACAAAGGCTGA | 23092 |
| rs145236293 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176692 | GGAGCCTGCGGAAGG[A/T]ATTACTTTAGTTAAG | 23092 |
| rs145250954 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220332 | GGTCGCTACTAGGAG[C/G]GGGTCTTGCTGAGCA | 23092 |
| rs145266966 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996158 | AACAAACCTGCACTT[C/T]CTGCACATGTATCCC | 23092 |
| rs145269411 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067215 | TTGTGATCTTTGAGA[A/T]GTTTCCCTTTGTGGG | 23092 |
| rs145274308 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920909 | CATTCTTACAGGGGA[C/T]GATGGCATGACTGGA | 23092 |
| rs145281163 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943060 | TTCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 23092 |
| rs145287201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828616 | TACTGTGTGTCTTTG[A/G]AATAATTTAAGAAGA | 23092 |
| rs145293156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963796 | TTATAATTCCTCTCC[C/G]TCCTTTAGAATGGCA | 23092 |
| rs145302017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899638 | CATCTCTGGAGTCCC[A/G]TGGGCTTCATCCTGC | 23092 |
| rs145307148 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832928 | GTTTTTTACTTAAAA[A/T]TTTTTTTTGATTATA | 23092 |
| rs145325821 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834245 | CAGTGAATACACTTA[C/T]GTAATGGCAACCCAG | 23092 |
| rs145332937 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913080 | TCCACTGCCCATGGT[C/T]ATGAGCACTCAGATT | 23092 |
| rs145338576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109070 | ATTTTAACTAATTAA[A/G]GATTGTTACAATGGT | 23092 |
| rs145344534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207044 | GTGGAGATTTGGTCT[A/G]GAGGAATGTGACATG | 23092 |
| rs145349913 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034582 | TTCCCACAGCTGGGG[A/G]AAGGGAAGACATGGC | 23092 |
| rs145358466 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981204 | CTTTGCTGCCCGACA[A/G]CAGGAGTTCAAGTCC | 23092 |
| rs145362778 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901065 | GAAGGGGCCAGGAAA[A/G]CATAACAACAGTGAG | 23092 |
| rs145365010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874740 | TTCTGACGCAACGCC[A/G]TGACAAAGGTTGAGG | 23092 |
| rs145369816 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804868 | TGAATTCTGCTCTCA[C/T]CATCATGCAACCACT | 23092 |
| rs145374103 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185503 | GAAAGTAAGCTGGCT[C/T]TGAATATTTGAATTA | 23092 |
| rs145382351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994452 | CTGTTAAGGGGTGAC[A/G]CAACCATAAAGGATT | 23092 |
| rs145389853 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918561 | CTCTCATCTCTGTGT[A/C]CACACCCTTTTGTAT | 23092 |
| rs145394739 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107628 | CTTCCCCTTTGAAAA[A/G]TATCTGTTTAGGTTT | 23092 |
| rs145394869 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149430 | AGCCATGTCAAAGTC[C/G]CCCATAAGCTCTGCA | 23092 |
| rs145395088 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032871 | TGAAAAAGAAGAGAC[A/C]AAGAGAGATGGGGGT | 23092 |
| rs145410315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031214 | GCCAGGCAGGGCCCC[A/G]TCACACACAGCTTTG | 23092 |
| rs145415969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130578 | CAGTGATTCTTCTCT[A/G]CAGACTGAAGAAAAC | 23092 |
| rs145418145 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196142 | TTTAGCAAACACCCC[C/T]TAAATAATACTAAAT | 23092 |
| rs145423385 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839365 | TAACAATCCTTTGAA[A/G]GTTTTTTTTTTTATT | 23092 |
| rs145436941 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122231 | TCCTTTTACTGTTAC[A/T]ACCTGATCTCGTCTC | 23092 |
| rs145453074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142959630 | TGTTGAATCCACCCT[A/G]TGCTTCACATCACTC | 23092 |
| rs145461597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008162 | CTGTGTTGAATATTG[C/T]ATATCTATGATTCCA | 23092 |
| rs145478046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836778 | AAACCTTTGGATCAG[A/C]TACCATACTAGGCAT | 23092 |
| rs145485108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143208591 | GGAAAAAGAAAACTA[A/C]AACACAGGGAGGTGA | 23092 |
| rs145491792 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106066 | AAGGGTCTTTTTAAA[A/G]GGTGACTTTTTCTTT | 23092 |
| rs145493704 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147772 | GTTTCCCTCCCCACT[A/G]ACTATGTTGGAAATG | 23092 |
| rs145500651 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847079 | GCTTGCTCTCGGTGC[A/G]CCTTGGGCAAATCAC | 23092 |
| rs145516000 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157412 | TGAACTCCTGACCTC[A/G]AGTGATCCACCTGCC | 23092 |
| rs145518906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998689 | TGATCGAGCCACTGC[C/T]CTACAGCCTGGGTGA | 23092 |
| rs145525312 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881721 | AGAGACAACAAACAA[A/G]CAAACAACAGATCCA | 23092 |
| rs145525645 | snp | A/C | 0.495855 | 0.045338 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986946 | gtagtgtgatgcctc[A/C]agctttgttcttttg | 23092 |
| rs145538144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896350 | TAATTGGCCCATCCA[A/G]CTTTTTTGAGGTGAG | 23092 |
| rs145551988 | in-del | -/GCTGTT | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783526 | TAATGAGCTGGTTGA[-/GCTGTT]GCACAGCAAGGGGAA | 23092 |
| rs145556721 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160740 | CACCTCGGCATCCCA[A/G]AGTGCTGGGATTACA | 23092 |
| rs145557943 | in-del | -/A | 0.0345262 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785616 | AAAAAAATTGCCAGT[-/A]ACTATCCTGATTTGG | 23092 |
| rs145558910 | snp | A/C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854708 | ACTTCGTTACTGATA[A/C/T]GAGACCGAGTAGACC | 23092 |
| rs145564131 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782279 | CTGTGGGAAGCACAA[G/T]TCTGGAACTCTGGAG | 23092 |
| rs145567832 | in-del | -/A | 0.0260105 | 0.111035 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939154 | GAGGGAACACTGCCT[-/A]AAAAAAGGCTGGTAA | 23092 |
| rs145613835 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084873 | AACGTGGTGAAACTC[C/T]GTCTCTACTAAAAAT | 23092 |
| rs145617932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111519 | GAGATAATTGAGGGA[A/G]TGGTTATCCCTGGCT | 23092 |
| rs145620132 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162060 | CAGCACTTTGACTTG[A/C/T]GCAATGCTGCTGGAA | 23092 |
| rs145620730 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070913 | TTGACACTATCGCAG[-/A]AAAAAAAAACAACAA | 23092 |
| rs145630322 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094485 | CCCCCAGAGGGGAAC[A/G]TAATCCCAGAGCAGC | 23092 |
| rs145635276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880065 | GTCAAAAAATGACAT[A/C]TGCAGGCCTGCTTCA | 23092 |
| rs145641233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924528 | TGATAATACAAGTAA[A/G]GTCCTTAGCACAGTG | 23092 |
| rs145646824 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050912 | CACCATCACCTTTGC[C/T]TGTTGGGATGCTTCA | 23092 |
| rs145649252 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809469 | CAAGACAGAAGTTGG[A/G]GTGTCTGAATATGTC | 23092 |
| rs145649811 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982418 | GGCTTCCCTCTGGGG[C/T]AGGACAGGGGGTGTC | 23092 |
| rs145651820 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821483 | TCCATTATAGTCTCA[A/G]AGTCATCTGTAACCC | 23092 |
| rs145675600 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882969 | CTTAACTACCCCACA[A/G]TAGACTCTCTGGAAG | 23092 |
| rs145685554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811706 | AGTTTAAGTGAGCCA[A/G]TGCATACAGAGCCTG | 23092 |
| rs145686145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193820 | GTTGTTCATCTCTTA[C/T]TATGCTTAAATGTAT | 23092 |
| rs145703831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883410 | CCTCAAATTTGAAGG[A/T]GTAATGTGTCCTCAG | 23092 |
| rs145706857 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812098 | TCCCCCTCCCCACCC[C/G]GTCTACTGCCTTTTC | 23092 |
| rs145716305 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787712 | TTAGATAACATGATT[A/T]TATAGACAATACATG | 23092 |
| rs145718417 | in-del | -/C | 0.170733 | 0.237101 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813836 | TAGGAATTTTAGGGG[-/C]CTCAATTCAGCCCTT | 23092 |
| rs145721403 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196463 | CCTGGTCACAACATT[G/T]TCATCACCTGATCAG | 23092 |
| rs145722567 | snp | C/T | 0.0162398 | 0.0886349 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228232 | GTTGATTCTAAAGTA[C/T]ATTTATGTGTGTGTG | 23092 |
| rs145727067 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769534 | TTATCAATCACCGTA[A/G]CACACACAGCACATA | 23092 |
| rs145740105 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091201 | GTGATGAGTCCATCC[A/G]CTTTCCGCTGTATGA | 23092 |
| rs145754691 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202885 | CATATGCAGAAAACT[A/G]AAACTGGACCCCTTC | 23092 |
| rs145764127 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785166 | CGATCTCCTGATCTC[A/G]TGATCCGCCCACCTC | 23092 |
| rs145765615 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975036 | TTGTCTGACGTGGTA[A/C/T]ATCCAACTTCAATCG | 23092 |
| rs145770989 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102473 | AATCTTTTTCCTCCC[C/T]TAACTCAGAATGCTG | 23092 |
| rs145774031 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167974 | ACAGAAACATAAAGT[A/G]CTTGTATTGAATGGT | 23092 |
| rs145775701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133659 | CAGACAGTGGCTTCT[A/G]TTGAGCACAGCTGCT | 23092 |
| rs145782298 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 5:142997807 | TGCTAAAGTGGTCCC[C/G]AGATGTAATGCTGAT | 23092 |
| rs145788293 | snp | A/G | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 5:143127439 | CTTCCCTAGTCCATC[A/G]GTTAGCTTTGGAAGA | 23092 |
| rs145790944 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940704 | TCCAGCCTGCTATTG[A/T]TGGGCATTTAGGTTG | 23092 |
| rs145795756 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055920 | TGTTTCCCTGTGATC[G/T]TTGTCTTCGAGAAAT | 23092 |
| rs145805319 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146040 | AGACTGTACTCTGAG[A/G]GATATATTGTAACAT | 23092 |
| rs145805595 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953825 | GTAGGTCTCTCCACC[A/G]TCTGCCTGAGATAGG | 23092 |
| rs145809449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859161 | ATAGGTTGTTCTGGG[C/G]AGCTGAGTGACAAAT | 23092 |
| rs145809831 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879614 | CTCATCGGTTCTTTA[C/T]GGGTGACTGAAGTAC | 23092 |
| rs145815883 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013326 | TTTGCCTCTTGGCCC[A/G]CAAAGCATAAAATGT | 23092 |
| rs145817891 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940473 | CCTCTCCCTCCTCCC[A/G]CCCTCCACTGTCAAG | 23092 |
| rs145826764 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970744 | CAGAAGTGGGAATGG[A/C]TGTGGGGCAAGTAGA | 23092 |
| rs145830255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842659 | GGGATTTAGAAATCT[C/G]TCTTGTCACCTATCA | 23092 |
| rs145835612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893265 | ATAGGCATGAACCAC[A/G]GCACCTGACTCCCAC | 23092 |
| rs145836777 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153280 | CTAGGTTTTAGTTCT[A/G]GCATCGACATTGCCT | 23092 |
| rs145839187 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213363 | CCCCATACAGGTGCA[C/T]GTGTGTGCTCATGCA | 23092 |
| rs145842828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829809 | TCCACCATATTGGCC[C/T]AATGTTTTCCACTCA | 23092 |
| rs145872099 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864965 | TTTGTACTTGAGCTG[C/G]CTGGAATTACCCTCT | 23092 |
| rs145875267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856048 | TGAAGAGTGAGGGAC[A/G]TCTCTTTATGTTATT | 23092 |
| rs145886662 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783670 | GCAACTCATTTCTGG[C/T]AAATACTGCTGTCTC | 23092 |
| rs145900701 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868783 | GTTTGACCTAGGAAT[G/T]GGGGTGTGGGCTAAA | 23092 |
| rs145917341 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141344 | ATGTGAGTCTGCTTC[A/G]TTAAAAAAGTACATG | 23092 |
| rs145917361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098809 | TATAACACATATTAA[G/T]AAATTAACACATTGC | 23092 |
| rs145926292 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022466 | TTATTTTTATAGGAG[C/T]ATTCAACTCCGCTAT | 23092 |
| rs145932590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027502 | TTTTTAAATATATAC[A/G]TATACTACTTTTATT | 23092 |
| rs145934808 | in-del | -/AATG | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196956 | AAGGAATATGGAAAT[-/AATG]AGGATAGACTGTATA | 23092 |
| rs145936986 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956569 | GTGACAGAGAGCCTG[C/T]CTCAAACAAAACAAA | 23092 |
| rs145939786 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841413 | CAGGACATCATTGCC[A/G]TTACGTTTACGGTGT | 23092 |
| rs145948711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912259 | TTGATATGCACAACA[A/G]TGTGGATGAATAGCA | 23092 |
| rs145950460 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845106 | TATCCTGAGGAGCTG[A/C]AGCTCTTGAGGGAGG | 23092 |
| rs145952236 | snp | C/T | 0.000134057 | 0.008186 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216315 | CTCTTGCTGCCATAA[C/T]CCCCTCTTTACAGAG | 23092 |
| rs145956119 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953091 | ACCTTGCACTAGCTA[G/T]TCCATGTAAGTTGTT | 23092 |
| rs145966339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102664 | CATTGCACAGCTCAT[A/G]AAATACCAGAGGAGA | 23092 |
| rs145967136 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137742 | CAGTCCGCAGTTGAA[A/G]TGCTTAGTGGGGTTG | 23092 |
| rs145981010 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024082 | TTGAATTACATTTAG[A/T]TGAGCTGTAATACCC | 23092 |
| rs145985120 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189787 | CCAGCCTGTGTTCTC[A/G/T]CCCACCCTACCTTGA | 23092 |
| rs145991515 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083906 | ATTTGCAAAGGTTGA[A/G]TTTCAAGTCATTATA | 23092 |
| rs145991618 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124444 | CAGAAATTTGAGAAG[A/G]GCTTATGTGTGCCCC | 23092 |
| rs145993863 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007114 | ACAGGTGAATCGCTT[A/G]AACCCAGGAGGCAGA | 23092 |
| rs146002111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010870 | TCCCTTGGATAGAAT[A/G]TTTGAATTTACTAGG | 23092 |
| rs146002835 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087055 | TGTTTGCCAGGGTCC[C/T]TGGCATTGTGACTCA | 23092 |
| rs146003189 | in-del | -/CACT | 0.125182 | 0.216612 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770467 | GGGAGGCGGCGTCTG[-/CACT]CGCTCGCCCGCTCGC | 23092 |
| rs146006656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025677 | ATTTGGAATTTTAAG[A/G]TGGACTAGGAGATTG | 23092 |
| rs146006794 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986984 | ATTGTTTTGGCAATG[C/T]GGCTCTTTTTTGGTT | 23092 |
| rs146022507 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804467 | CCAAGCATATTATTA[A/C]GCATAGGTTTGAACA | 23092 |
| rs146024762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218127 | ATGCCTTTGTGTCTG[C/T]GTGTTATCTGTGGCA | 23092 |
| rs146033795 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806662 | GAGTGATGCCTGGAC[A/G]ACATCACAGTGAAAG | 23092 |
| rs146034563 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187245 | TATCTGACCCTAAAC[C/T]CCTGCACTTAACTGT | 23092 |
| rs146037782 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027173 | CCTTCATGATTTTTT[G/T]TGTTTTTTTTTTTTT | 23092 |
| rs146040789 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121764 | GAATATTAACGCAGA[A/G]CTGCCCTTGTAAAAC | 23092 |
| rs146056187 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009381 | AAGTGCTTGGGCTCT[A/G]GAGACAGACCGTGGG | 23092 |
| rs146056291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938493 | GCTCAGGAAAATTTT[A/G]GAGACAGCAGAGTTT | 23092 |
| rs146058127 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890735 | AACCACCGACATGCA[C/T]GGGACACTTTCCAGT | 23092 |
| rs146062313 | in-del | -/ATTT | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104907 | AAAACATTGAATAAC[-/ATTT]AGTTATTTCTGGATG | 23092 |
| rs146070333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894053 | TGTATTTAAGTTGTA[C/T]AATATGATGTTTCAG | 23092 |
| rs146072851 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825855 | TGGCGGAATCCCTCA[C/G]AACACAGTTCTCGAA | 23092 |
| rs146074352 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202754 | TGGAACAGAACAGAG[G/T]CCTCAGAAATGACGC | 23092 |
| rs146089456 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121226 | CCTTCAGAGTTGGCT[C/G]AGATTTGCATTGCTA | 23092 |
| rs146106500 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005905 | GCCTAGTCTTGAGAT[A/G]CCTCTGATTGTGTAG | 23092 |
| rs146108546 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174508 | TGGAGAGGGAAGGAA[A/G]AGTTATTTTTCCTGT | 23092 |
| rs146114263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065744 | CCTGGAGCCTCATGC[C/G]TGCGTTTCTTACCTC | 23092 |
| rs146123155 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069680 | AATGTCAGCTGTTTA[C/T]AGGAGTTGTGCTTGC | 23092 |
| rs146144669 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830942 | TTTTCAGACAGGCAA[A/G]TATGACCTTGCAGAT | 23092 |
| rs146147322 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204739 | AAACTATGCCATTAG[C/T]CAAAGGCATAATTCT | 23092 |
| rs146158503 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170647 | TGTGTACTTATTTAA[C/T]CAACATAATGCCGGA | 23092 |
| rs146180094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916377 | ATTACCGTACATCAA[C/T]GTATTTTACTGTGGT | 23092 |
| rs146181678 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874377 | CATCAAATGCTTATT[A/G]AGTTCCTGTTGCCAT | 23092 |
| rs146191180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878743 | AATAGCCAAATGCTA[C/T]GGCCCTGAGGTGGGA | 23092 |
| rs146194327 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193610 | CCCCAAAGTCCAAGA[-/G]TGGTAATGCTGGCAA | 23092 |
| rs146194800 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806988 | AGTGTGAAGGGAGCC[C/T]TCAGGCTTGCTATAC | 23092 |
| rs146201035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912422 | ACTAGGAGGAGGGAT[A/G]GATTGCCAGGGGATA | 23092 |
| rs146219226 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136953 | ACACACCTAGCTCAG[G/T]GCTTCCCAAATGCCA | 23092 |
| rs146227230 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990902 | CCCAGTTAGGCTACT[C/T]GGGGGTCAGGGACCC | 23092 |
| rs146230146 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118203 | ATATGGACAAAGGCA[A/G]AGAGGTGTGGAAGTG | 23092 |
| rs146235085 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043517 | AAATTTTCATATATA[A/G]TTTCTGTGTGAGCAT | 23092 |
| rs146238471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200317 | AGCCTTTGACCCACT[A/G]ATTTTACTTTCAGGA | 23092 |
| rs146246369 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047872 | TGCCCAGGCTGGAGT[A/G]CAGTGGCTAAGTGTT | 23092 |
| rs146268741 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210610 | CCCCAAAAAAGCCGA[C/T]AGCCCCAAACCCGTA | 23092 |
| rs146278425 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156143 | ATTGTTTCTACCTCT[A/G]TGTATTTAATCTGAG | 23092 |
| rs146281937 | in-del | -/T/TGG | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768900 | ATTTTTTGTAGAGAT[-/T/TGG]GGGGGGGGTCTCGCT | 23092 |
| rs146288263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215141 | TTGCAGAAGACAAAC[C/G]AGAATGGGCTGCGTT | 23092 |
| rs146296865 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978022 | CCTCTTGACTCCTCT[C/G]ACTTATTTTCAGTGA | 23092 |
| rs146309036 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933975 | CACTCACTCCCTTGA[A/G]TGATTCTTCAACTCA | 23092 |
| rs146311983 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861317 | TTTCTGGGAATGTTA[C/T]TAGGTGTGGCTTTGT | 23092 |
| rs146315141 | in-del | -/AGGTAGT | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110484 | ACAATGTTAGCTTAA[-/AGGTAGT]AGGTTGTGTGGTTGA | 23092 |
| rs146319464 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894560 | CAATGGAGATAGAGC[A/G]TCCAGCAGTCATTCC | 23092 |
| rs146346061 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973493 | AATCGTTGAAATGTT[C/T]GGGGAGCGAGAATAG | 23092 |
| rs146350904 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204519 | ACAAGAGCAAAACTC[C/T]GTCTCCAGAAGAAAA | 23092 |
| rs146353428 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189346 | CAGTGAGCCCTCAGC[-/A]AGTCTACTTTGTTGA | 23092 |
| rs146354666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101306 | AGTGTGTCATTTCTC[C/T]TTCTCATAATTTTTT | 23092 |
| rs146354784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024660 | TCACTGCTTGATATA[C/T]GTTATGTCATTTGAT | 23092 |
| rs146355381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954684 | TGCAGTACATGTTGT[A/G]TAAGCATATGAAACT | 23092 |
| rs146355456 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143167 | CCCATGCATGGGGGG[A/G]AACCTCCCGCAAATG | 23092 |
| rs146366614 | snp | C/G | 0.0603597 | 0.1629 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103736 | CACTCGTAAGTGGGA[C/G]TTGAACAGTGAGAAC | 23092 |
| rs146366824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028779 | AGCTCATTCAGTTTC[C/T]ACTACCTACAATTCT | 23092 |
| rs146385452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820398 | TTTTCCCTGATCAGT[A/C]ATTTTGTGGTTGGGT | 23092 |
| rs146395501 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824476 | CTGCAGCCCTAGCAT[C/T]AGCAGCTGTATAAGC | 23092 |
| rs146403439 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140103 | AGATGCTTGGTCTCC[C/T]ACCCAGGATATTCTG | 23092 |
| rs146419133 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988841 | TCTAGTTTGATTGCA[C/T]TGTGGTCTGAGAGAC | 23092 |
| rs146423271 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796675 | GGCTTTCTGAGCCCT[C/G]TGGACTCTGGCCCCT | 23092 |
| rs146424336 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998830 | CTGTGCAACACGAGA[C/T]GGTGAGCTAGTCTGA | 23092 |
| rs146433704 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800759 | CCACAACTATTCTCG[C/T]GAACCTGGCAGCACG | 23092 |
| rs146435083 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181526 | GTGGGGCACTTATCA[A/G]TGTGTTGTCATCACC | 23092 |
| rs146441695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837880 | AGAATAGTTATTTAT[A/G]TACATAATTTCACAG | 23092 |
| rs146444461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208829 | AATTCTTTTTTTTCT[C/T]ACTCTATAAATAAGG | 23092 |
| rs146453822 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211984 | TTTTATTTCTGGCTG[C/T]CAAATACCCCTGCTG | 23092 |
| rs146460865 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843455 | ATTGTCATGATTACA[A/G]TGATGCCTACCATTC | 23092 |
| rs146469647 | in-del | -/GTGTGTGTGTGTGTGTGTGT | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867309 | TAAGATTTGCACAGG[-/GTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 23092 |
| rs146470193 | in-del | -/GT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947094 | TCTTTATTTTTAAAA[-/GT]AAAAAAAAAAAAAAA | 23092 |
| rs146481229 | in-del | -/T | 0.0554779 | 0.157039 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962602 | CTGAATGGTGAAAGG[-/T]TTTTTTTTTGGTTGT | 23092 |
| rs146482451 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889340 | CTAGTAGGCCAGGCA[C/T]GGTGGCTCATGCCTG | 23092 |
| rs146490678 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969058 | TGCCTCAGCCTCCCA[A/G]TTAGCTAGGACCACA | 23092 |
| rs146491406 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891101 | ATCTCTCCGTGTAAG[C/T]GTGTTGGATTTGCGC | 23092 |
| rs146493195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851258 | TGTGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 23092 |
| rs146495581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877580 | TGAGAAAACAGGTCT[C/T]ATTAAGGCTGATAGC | 23092 |
| rs146510328 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184284 | GCTGAAATACTCATT[A/G]CAAATATTCAGGCCT | 23092 |
| rs146516692 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118652 | TGGCGCATGCCTGTA[C/G]TCCTAGCTACTCAGG | 23092 |
| rs146516702 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078811 | TGGAAAAATCAACTT[C/T]AGAGACTTTCTTAGC | 23092 |
| rs146530306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002483 | TGGTCTCTCCTCTCA[C/T]CATGAAAACGGCATG | 23092 |
| rs146532911 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097600 | TCGAGGCGGGTGGAT[A/C]ATGAGGTCAAGAGAT | 23092 |
| rs146563118 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839093 | ATAACCAGGGATCTG[C/T]ATTTTAACAAACATT | 23092 |
| rs146563849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888807 | AGTCTGTCCAGGCAC[C/T]GGGTGTTTTGTAGAA | 23092 |
| rs146566095 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816040 | TGGGCTGAAGCCGTC[C/T]ACCCGCCTGGGCCTT | 23092 |
| rs146567449 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196473 | ACATTTTCATCACCT[C/G]ATCAGTACACCACCC | 23092 |
| rs146577686 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775971 | GGAATTGACATACCA[A/G]TTGATCATGGTTGTC | 23092 |
| rs146578365 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199144 | TTAAATTATATTAGA[G/T]GAGGGGAAATAATCT | 23092 |
| rs146599494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944325 | TTTGATGACATCATT[A/G]TGAACAACGGCTTGG | 23092 |
| rs146612239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947663 | GAGGCAATAAATTGA[A/G]TGGTTTTCTGTTAAC | 23092 |
| rs146613634 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834257 | TTATGTAATGGCAAC[C/G]CAGGCCAAGCAATAA | 23092 |
| rs146635091 | in-del | -/AAG | 0.435119 | 0.16802 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958922 | AAAAAAAAAAAAGAA[-/AAG]AAAAAAAAAGAAAGG | 23092 |
| rs146646425 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060757 | TCAGTCAGGCTCGCT[G/T]CCTGGGAATCTGCAT | 23092 |
| rs146652790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149366 | TCCTGAGGTAGAAGC[A/T]GTACCAGCATCAGCC | 23092 |
| rs146676871 | in-del | -/TA | 0.0622301 | 0.165053 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962534 | AATCTTTTCCCAGGT[-/TA]TATAGGCTGCCAACC | 23092 |
| rs146682997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870624 | TGAGGAAAGAATAGC[C/T]CAGCTATACCTAGAA | 23092 |
| rs146685523 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801158 | TTTTTAACATTTTTT[C/G]TGGGCATAGCTTTGA | 23092 |
| rs146690142 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181911 | CTCATGGTCTACATG[C/G]TCAGCCATTGTTTAC | 23092 |
| rs146701290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184833 | GAGGAGGGAAGGAAC[A/G]TGTGTGAGGCCAAAT | 23092 |
| rs146719153 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926833 | ACCCCATACTTACCA[G/T]CCTGTTCCTGCTCAC | 23092 |
| rs146728696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123346 | CAGGCCTAGCCTGGT[A/G]TGAAGTAAGGAGATG | 23092 |
| rs146730094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931290 | TAGAGGGCTTTCAGC[C/T]GCTTCTCCCAAGGTC | 23092 |
| rs146730694 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884000 | TGTCTGAGCTTCTTT[A/G]TTTGGCCAGAAAATA | 23092 |
| rs146732241 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083086 | TCGAAGGCAGTCTCT[A/G]TGTATCTTGGGGAAG | 23092 |
| rs146732386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004558 | GGATGCTGGGTCAGC[C/G]TCCTGCTTTAGTGGA | 23092 |
| rs146755236 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152705 | GCCTTCCCAGGCCCA[C/G]GCCACAATGCCTCAC | 23092 |
| rs146755427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036608 | CTTAACTCAGGGACA[C/T]GTTTAAGGCAGTTTG | 23092 |
| rs146756341 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200484 | TACCATACAATAGAA[-/C]CAGCCTGTAGCCATT | 23092 |
| rs146757095 | in-del | -/TT | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943899 | TTAACCTTTGGGGAA[-/TT]TAGGATTAGTTGTGA | 23092 |
| rs146765883 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114845 | TTGGTATGGCCTCCA[A/G]TGGTCAGTGGAGTGC | 23092 |
| rs146766496 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040262 | GTGAATCATGCAGAA[C/T]GATGTACATGATTTT | 23092 |
| rs146774922 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131768 | GCATCATGGGATGCA[C/T]CTGCCTAGCATAGTG | 23092 |
| rs146798883 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196395 | AAACACGGAATTACT[A/G]AATACTAAGCCATTG | 23092 |
| rs146799249 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873065 | CAGGCTGTGGACACT[-/A]AATGTTGGCTCTGAT | 23092 |
| rs146804065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853860 | GTTTCTGTTTGTAGT[A/G]TAATGGGAAACACTA | 23092 |
| rs146806843 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781804 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 23092 |
| rs146811949 | in-del | -/TT | 0.179105 | 0.239737 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785978 | GACTGATCCCTGGTA[-/TT]TTTTTTTTTTTTTTA | 23092 |
| rs146815966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967616 | GAAACCCCATCTCTA[C/T]TAAAAATACATCAGT | 23092 |
| rs146816165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085269 | GCTTCATAGAACATC[C/T]TCTGGTGGCAGATAG | 23092 |
| rs146816518 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193127 | TGAAGTCCTGCTCCC[C/T]GGGACAGGAATCATC | 23092 |
| rs146817549 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227116 | CTGGCTTCTGCTCCC[A/G]AAAGCAAGTCTGGAT | 23092 |
| rs146843007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904879 | TCCTAATAGCTTTCC[A/G]ATGGGATAGAATAGA | 23092 |
| rs146849542 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988448 | AAAAACTAGCTGCTG[A/G]ATTCATTGATTTTTT | 23092 |
| rs146853951 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868683 | CGTTACACTGGGGAT[G/T]CAGGAAGAGGCCCTC | 23092 |
| rs146854421 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909395 | AGTAGGGGTTAAAAG[C/T]GCTGGCTTTGCTCTC | 23092 |
| rs146860881 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858114 | GAGAGAGAGAGAGGG[A/G]GTGTGTGTGTGTGTG | 23092 |
| rs146871851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198718 | ATTCCAAAATCTTGA[A/G]TTTTGTTTAAATCAT | 23092 |
| rs146876900 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017277 | TTCTCTCAGGGCATA[C/T]GGTGCCTGTGGAGTA | 23092 |
| rs146877015 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135101 | AGTCAGCATCACAGC[A/T]GCTTCATTAGAGATA | 23092 |
| rs146888522 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097064 | CAAATACAGACCATG[C/T]GCGGTGGCTCATGCG | 23092 |
| rs146899082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802462 | GGCTTTAAGTAAAAT[A/G]GATTCTTGAATAATG | 23092 |
| rs146903334 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216924 | GACCCTCTTCCTCCC[C/G]ACTCCTTCACCTCTA | 23092 |
| rs146903683 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182528 | TTTGTTAAGTGAATC[C/T]GTTTTAGTTTAAAAA | 23092 |
| rs146909805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805019 | TGAAGCATGTGTCAC[A/G]AGCTTATTCCTTTTT | 23092 |
| rs146913669 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185820 | TGTCACAAGGCTGGC[A/G]AGCAGAGGAGTGAAG | 23092 |
| rs146916883 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120256 | GATACATCTTTTGAG[C/T]AGTTGTTTATTCAAA | 23092 |
| rs146941331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892028 | CAATTGTACCCGCTC[G/T]TGGGCCTGTCCTGGA | 23092 |
| rs146944215 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003719 | GAAAAGGGAAATAAC[A/G]TTTTTGAGCACCTCC | 23092 |
| rs146948830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932673 | GAGTACAGTCTAACT[A/G]TGTGCCACCAACAAA | 23092 |
| rs146954969 | snp | A/G | 0.000131996 | 0.00812284 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143054469 | CTGAGACAGAAACAG[A/G]TATCTGTGCTGAATG | 23092 |
| rs146957791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889761 | GAGCTAATGAAAGGC[C/T]AGGACAATCTTCTTC | 23092 |
| rs146959960 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817759 | TCGCCAAATTGCACT[A/G]TTTGCCCCTGCTGCA | 23092 |
| rs146963763 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097360 | CCGTCTCAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 23092 |
| rs146977743 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063034 | CATACACCCTGGCTC[C/T]GGAACCTTTGTTCTC | 23092 |
| rs146981622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990340 | CTACACAGTTTATTC[C/T]AGTTAGCTATTTGTC | 23092 |
| rs146987723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067927 | CCAGCACTTGGGGAG[A/G]CCAAAGCAGGCAGAT | 23092 |
| rs146988938 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991967 | AATATCCATTTCCCT[A/G]AGCCTACATCTATAC | 23092 |
| rs146993105 | in-del | -/CT | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222554 | ATGCAGCGTGACTGA[-/CT]CTGTTGCTACCTGTC | 23092 |
| rs147006812 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165612 | TGTGTAGGTTTGTTA[C/T]GTGGGTATATTGTGT | 23092 |
| rs147017334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169148 | TCCTGTCTTCCTCAC[A/T]TGTTTCTGAAAACTG | 23092 |
| rs147022805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102939 | TGTGGTAGCCACAAA[C/T]GTTTATATAATGCCT | 23092 |
| rs147024489 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186363 | CCCTGTCCCCACTCC[A/G]TCTCCACATGGGGCT | 23092 |
| rs147048948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805582 | TTTGTATTTTACTTT[C/T]AGCAGGTTTTTGAGG | 23092 |
| rs147052697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911190 | GGAGCAGCCCAAAAC[C/T]GATCCTATCCCTTCT | 23092 |
| rs147062379 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914121 | CAAGCCAGTACTCAC[A/C]CCTCCCTGGGAAGTT | 23092 |
| rs147063891 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872126 | TGTATCCAGTGCCCC[C/G]ACTCCCACCGCCCCC | 23092 |
| rs147088736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119229 | GGAAAAATGATCATC[A/G]TCCAAACCGTGTATT | 23092 |
| rs147112426 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150717 | GAACAACTGGACATC[C/G]ATATACACAAAAATG | 23092 |
| rs147112474 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189318 | CCATAAAAAAGATGC[A/G]CTTGGGCTTAAGACA | 23092 |
| rs147122011 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153683 | GCAATGATGGAACCC[A/G]ACCTTGGAGTTCTCT | 23092 |
| rs147127025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085807 | GAGGAAGGAAACAAA[C/T]CTCCTTAACCGAAAG | 23092 |
| rs147132237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129806 | CCTACTCTTTGCCAC[A/G]TACTGCACTGAGCAT | 23092 |
| rs147132754 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059825 | ATCTACCTGTAGACA[A/G]GCTCTCATGCTGTAA | 23092 |
| rs147142462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016117 | AGCCTTTAGAAAGAA[C/G]CAGAGAGGGCTGGAT | 23092 |
| rs147160560 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779207 | ATTTTTACAAATTAT[A/G]GTGACTGGGGTTTAC | 23092 |
| rs147162133 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221616 | CCTGCTGAGCCCAAG[C/T]GATCCTCCCGCTTCG | 23092 |
| rs147171803 | snp | A/C | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225440 | GTGATCTGCCCACTT[A/C]AGACCCCCAAAGTGC | 23092 |
| rs147174860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127156 | AAAACAAACTGCTTG[C/G]TTTTCATAGTTTTGG | 23092 |
| rs147175416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143166192 | GAACAACCCCATGTA[C/T]GTAGCTGGCAGTGAA | 23092 |
| rs147189267 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982808 | GGGAGGAAGATGGAC[C/T]AGAAATTGATGTGAG | 23092 |
| rs147189956 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902953 | GCTGTGATGCAGATG[C/T]AGCAGAGGTCTCAGT | 23092 |
| rs147199508 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905842 | ATATCAAATTTAACA[C/T]TGGTGCAATATTTAA | 23092 |
| rs147202501 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794981 | GCAAGCTTTTTCTGT[A/G]AAGGGCCAGTTAGTA | 23092 |
| rs147221601 | snp | C/T | 4.98575e-05 | 0.00499262 | missense, upstream-variant-2KB, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770901 | ACGGGAAGTCACTCA[C/T]AAGCGCGCTCAAGAG | 23092 |
| rs147222722 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848516 | TGGTTCTCCAGCCTT[-/G]GCACATCAGCTGAGT | 23092 |
| rs147230593 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095713 | GGGTAGCAGGGATTA[A/C]AGGCACCCGCCACCA | 23092 |
| rs147231579 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018722 | CCCAATACCTCTCTG[C/G/T]TTTTAATAATAACTT | 23092 |
| rs147232594 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179113 | GACCTTAGCGATCCA[C/T]CTGCCTCAGCCTCCC | 23092 |
| rs147247259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997218 | TTTGTGAATTCATCT[A/G]CTCACCAAAATTTAT | 23092 |
| rs147247925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076348 | GCACTTTTTAAAATT[C/G]TCTAAGACAATGTAA | 23092 |
| rs147247940 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115904 | TGCAAATTGGAGAGA[A/G]TATTTGCACTTTATA | 23092 |
| rs147263967 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835921 | AAGATTAGTTTTAGT[A/C]TTACACCCATTTTAT | 23092 |
| rs147266474 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207810 | CCTTTTCTTTTCTCA[C/T]GTTTATCAGGCAGCG | 23092 |
| rs147276557 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210078 | TTCTGAATGATGTCT[C/T]CTCTGGAAATTGCTT | 23092 |
| rs147294228 | snp | A/G | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961307 | ACTAGCCTGGGCAAC[A/G]TGGTGAAACCCCATC | 23092 |
| rs147297964 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887169 | TTCTCTCCGTGGTCA[A/G]ATATTGCAGACTTGG | 23092 |
| rs147310143 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774561 | ACAGTTGTTATAGTT[C/G]ATGAACCAATATCAA | 23092 |
| rs147330234 | in-del | -/C | 0.0577344 | 0.159793 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769967 | GTGTAAAATCGGTTG[-/C]CCCGCAGTGCAGGGC | 23092 |
| rs147337660 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001007 | TATGTAACAAACCTG[C/T]ATGTTCTGCACATGT | 23092 |
| rs147338151 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080768 | GAGGGTTCTGAGGGT[A/G]TGAATGGCACAATCT | 23092 |
| rs147338315 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957453 | CCTCCAAGACCATCA[C/T]TGGACCATAAGATAT | 23092 |
| rs147339532 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162947 | ACAACATGACATACC[A/G]TCTCTATTAAAAAAA | 23092 |
| rs147352744 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053991 | AATCATTCTTCTATC[A/G]TTGGACATTTAGGTT | 23092 |
| rs147355051 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099345 | AATATAGAATTGCCA[G/T]TGTTGGTTAACTTGG | 23092 |
| rs147356602 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983515 | CCAGCCTGGTCCTTT[C/G]TTTCTATTGTTTTCA | 23092 |
| rs147358069 | in-del | -/GGG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190028 | TGGAGGACAGAAGGA[-/GGG]GGGGGAAAAAAAAAA | 23092 |
| rs147365011 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778170 | TCTAGAATGATTCAG[A/T]TATTTTTGGCCTGAG | 23092 |
| rs147371276 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814297 | TGTTCTTCCTGTTAG[A/G]TGTGCTGTAAACAGC | 23092 |
| rs147381321 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772474 | TCTCTGCTTCACTCA[C/G]CAAACTTTTGGTGTG | 23092 |
| rs147382025 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197965 | GAATGTCTAGTCCAT[A/G]TCTGTACATCCAGTT | 23092 |
| rs147383123 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160564 | ATCACAGCTCACTGC[A/G]GCCTCAACCTCTTAG | 23092 |
| rs147403414 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869852 | CAAGAAAAGAAGGGC[A/G]CTTCCTCTAGTCCCT | 23092 |
| rs147412531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945394 | TTAACGCTACACACA[A/G]TTTTATATTTTCTGG | 23092 |
| rs147413152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873142 | CAAACGGAGATGACA[A/G]GTTGCCTTTAGAAAG | 23092 |
| rs147413554 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832594 | TTTCAGGTCTTTTGT[A/G/T]TGCCTGGCACAGGAC | 23092 |
| rs147419128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939185 | TTGGTTGATCTCGGA[C/T]AGATGATTCAGGTCT | 23092 |
| rs147441481 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143058871 | CAAAGCCACAGTTGC[A/T]CCATTATTGACCAAC | 23092 |
| rs147445127 | snp | C/T | 0.00172802 | 0.0293432 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147402 | TATGATGTCCAGCTG[C/T]CTACCCCACAAGGGC | 23092 |
| rs147447746 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081066 | TCACTGGGGGAGAAA[A/C]GGAGGTCTTGTCTTG | 23092 |
| rs147460297 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034507 | ATAAAAGACCGCATC[A/G]TGTATGATTCCCATT | 23092 |
| rs147474987 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869421 | AGATGAGGTTTCACT[A/G]TGTTGGCCAGACTGG | 23092 |
| rs147477294 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799543 | GTAGGAATGACATGT[A/G]CCTTAGTTCGTTTTG | 23092 |
| rs147478151 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179813 | CTACTCTTAAAACTA[A/G]ATATAGGAATGCCTC | 23092 |
| rs147487764 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182733 | GACAAATCCCTTGCT[C/G]TATGTGTGTGGTGGC | 23092 |
| rs147488161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143832 | GCATCCTTAAGGACC[A/C]AGTTCACATGCAGTT | 23092 |
| rs147509624 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853191 | TATTTTTTAATTTTA[C/T]TATTATTTTTTGAGA | 23092 |
| rs147518141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929289 | GCCCTGCCCATTTTT[C/T]GCTATGAAGAACCAC | 23092 |
| rs147524757 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968048 | ATCCGGAGCAGCTTT[A/G]CTTCTTGCTTCTCCT | 23092 |
| rs147558491 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939503 | TACCGTGCCCGAGCT[C/G]TAACCCCCTAGTCCT | 23092 |
| rs147569180 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828739 | TCATGTAGGGGATTG[A/T]CTCTATATTTTGAGG | 23092 |
| rs147578261 | snp | A/T | 3.2969e-05 | 0.00405998 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143056040 | CAGAATGCTTCCAGG[A/T]CCACTCATGATGTAC | 23092 |
| rs147587546 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049801 | CATTGATTTTTCCTG[A/G]TTTTGGTATTTGGTC | 23092 |
| rs147587728 | snp | A/G | 0.027192 | 0.11349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123101 | CCAGCCTCCAAAATG[A/G]CTCCCAGTGATCCTG | 23092 |
| rs147594828 | snp | G/T | 3.29468e-05 | 0.00405861 | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207323 | GGTCTGTTGCAGGGT[G/T]TGTTTGGTTTTCTGT | 23092 |
| rs147597506 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008428 | GATGAGATGATATTC[A/G]ATGGTGTAGAACCAG | 23092 |
| rs147597562 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055210 | CCTAGTCTTAAAAGG[A/G]GAGGGGAATGGTCAT | 23092 |
| rs147601000 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936176 | GTAGGTGAGTTCAGC[A/G]AGGTCACAGGATACA | 23092 |
| rs147603682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136763 | CTGTGAAGTTTTCAC[A/G]CACTTCACCTTTCTC | 23092 |
| rs147625969 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176753 | TAGGCAGAGGTCTAC[A/C]TTTGGCATTGAAACT | 23092 |
| rs147629187 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899747 | AGGTGCTGGGAGGAG[A/G]GAAGCAAGGGGGAAG | 23092 |
| rs147631906 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787257 | ATCATTGGGGTGGGA[A/G]AGTGCCATTAAAATG | 23092 |
| rs147641980 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791634 | AGATTTTGAATATTA[G/T]AGTATATATTCTCCT | 23092 |
| rs147646763 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143172967 | TCCATAGGGTTCATG[C/T]GAGTTCAGCAAGCAG | 23092 |
| rs147652266 | in-del | -/CA | 0.0425829 | 0.139564 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881665 | TCCTTTGCATCACTC[-/CA]CACACACATACATTT | 23092 |
| rs147658032 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096697 | GGCTTTTTTTTTTTT[-/T]AATCTGTGAGTGTGT | 23092 |
| rs147660235 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070445 | CGCATAAATTTAACT[A/G]AGACGATTGAAAACT | 23092 |
| rs147669646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954093 | TGTACAAATATTATG[C/T]GTTCTAACCCCACAG | 23092 |
| rs147672714 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880269 | TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 23092 |
| rs147693085 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106346 | GTTCGCATCATTGTG[C/T]GGGTAACCACATGGT | 23092 |
| rs147694055 | in-del | -/TCCTGGAGAGTTGAG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009925 | GTCCGCTTGGGTTGC[-/TCCTGGAGAGTTGAG]TTCTATTGTATTAAG | 23092 |
| rs147704654 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991766 | TAGCCTAGTTGTGTA[G/T]TAGGCTATACCATCT | 23092 |
| rs147708349 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161139 | GCCTCAGCCTCATGA[A/G]TAGCTGGGATTACAG | 23092 |
| rs147708573 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119292 | ATAAAAAAATAGCTT[C/G]TTGATTCACTTGCAC | 23092 |
| rs147718577 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845950 | TGTTTCCTCACCCAC[A/G]CTTCACTCACATGCC | 23092 |
| rs147731462 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219161 | TGGTCTCTGGAGTCA[A/G]ACAAGCTGGGTTCAA | 23092 |
| rs147734162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843271 | CTTCCCAAGCATGCA[C/G]CTGAGGCAAAGAGTG | 23092 |
| rs147734537 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883101 | TTCTCAGGACAGAAA[C/T]GGCTTCCCTTTCTCC | 23092 |
| rs147746184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216778 | CCAAATTGAACCTGA[A/G]AGAAAACACCTCTCA | 23092 |
| rs147761771 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048606 | TATCTTTTTTCTAAA[C/T]GAATTATGCCATAGA | 23092 |
| rs147766518 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980483 | AACCTCCGTTTCCTG[A/G]GTTTAAGCAATTCTC | 23092 |
| rs147766528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932520 | TGGCCTCAGCTGGGT[A/G]ATGTAATCTTGTAGT | 23092 |
| rs147776267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935986 | ACTCAGCAGAGGACT[A/G]GAAGTCCTAGTCAGT | 23092 |
| rs147792635 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157042 | AATAGCTCTCAGGCT[A/G]TGTGATACTGAAGGT | 23092 |
| rs147794688 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088510 | TATTATTTTCAAGGT[A/G]AGGACCTCCTATAAC | 23092 |
| rs147804608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044985 | TTTCAAAGATGACAG[A/G]TTATTATGTAAGATG | 23092 |
| rs147807718 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092659 | GAAGTTAGGATAATA[C/T]ATGTTACACTGTTAA | 23092 |
| rs147809086 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975146 | GTTTGTAATGGAAAT[A/G]ATGGTAGACTGAGCA | 23092 |
| rs147813570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143899 | TGCCAATGCATGCTT[A/G]CCATTATTTGGGGAT | 23092 |
| rs147814049 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102677 | ATGAAATACCAGAGG[A/G]GAAAGCTTGCTTTCT | 23092 |
| rs147823864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826992 | TTTTCATTTTCTTTC[C/T]TTGTGTCACTTGTCA | 23092 |
| rs147834311 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205841 | GTAATGATTTGTTAA[A/G]TATAGTACCTACAGA | 23092 |
| rs147839723 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822320 | TGATTATATGTTTTC[C/T]GGTGACATACATGCT | 23092 |
| rs147840389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867849 | TTGGAGAGTTTGTCC[C/T]AACTTACCTGCTTTT | 23092 |
| rs147866000 | in-del | -/ACAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222247 | CCAAGCTTCCTTCAT[-/ACAC]ACACACACACACACA | 23092 |
| rs147869460 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030242 | TAGCGGAGAATACTT[A/G]TGTTTTCCAGGGGCT | 23092 |
| rs147870133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957919 | CAAACGTACTTGAAC[A/T]GGGCATAAGCCTTTG | 23092 |
| rs147880261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913862 | ATTCCTCGAGATTTA[C/T]AGAGTCTCTCATTAA | 23092 |
| rs147883902 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846158 | TGCTCACATTTATAG[C/G]TGACTCATGTTGAGT | 23092 |
| rs147891891 | in-del | -/CT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850373 | TTCTTATTACAGATG[-/CT]CTCTCTCTCTCTCTA | 23092 |
| rs147898126 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140970 | TATTCAAAGGCTTAC[A/G]TAATGCCTTTCTCTG | 23092 |
| rs147900661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071147 | AACAGAATAGAGAAC[C/G]CCTAAATTAATCTGA | 23092 |
| rs147905979 | in-del | -/C/CCC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222271 | ACACACACACACACA[-/C/CCC]CACACACACACACCC | 23092 |
| rs147910537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077511 | CTCTTAACCCTCTGC[C/G]ACAAGCCTCCCTAAA | 23092 |
| rs147912936 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025485 | AGCTGATGATGATCT[C/G]TTTCGGTTGAGAAAT | 23092 |
| rs147913562 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954707 | ATGAAACTTGACTAG[C/T]GTCCAGTGGTGATAT | 23092 |
| rs147916914 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085271 | TTCATAGAACATCCT[C/T]TGGTGGCAGATAGTA | 23092 |
| rs147929930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808939 | ACTTATTAAGCTTGT[C/G]TCCTTGTCCTTTCTA | 23092 |
| rs147935644 | in-del | -/GATGAT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028166 | TATCTACAAAATACG[-/GATGAT]GATGATGATGATGAT | 23092 |
| rs147940618 | in-del | -/CC | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154114 | AACTCCTACTGTGGG[-/CC]CCTGGTGGTGGTCTG | 23092 |
| rs147941706 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191790 | CCAAGTTTATGCCCA[A/G]TGTGCCTGTCTCCCT | 23092 |
| rs147943503 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918353 | GGTTTCACCATGTTG[A/G]CCAGGCTGGTATCAA | 23092 |
| rs147946226 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849823 | TCTGCTTCACCTCCC[A/G]TGCTCCCTGTTTCTG | 23092 |
| rs147947107 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805252 | GGATTACAAGCATGT[A/G]CCACCACACCTGGCT | 23092 |
| rs147958400 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188980 | CCAAAATGGAACAAG[C/T]GACATACTCTTTTAA | 23092 |
| rs147983433 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927782 | TATTCTCCCATCAGC[A/T]ATGTATGAGAGTCCC | 23092 |
| rs147986767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855873 | TACTGTTGTCTCTCC[A/G]GTGACTTATTACCAG | 23092 |
| rs147990085 | snp | C/G | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225222 | AGATGGAGTCTCACT[C/G]TGTGGCCCAGGCTGG | 23092 |
| rs147992284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141746 | AGTCTCACATAGAAA[A/G]GAGGGCTGTCTTGTG | 23092 |
| rs148005328 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033414 | GTATTTGGAAGCGTC[C/T]ATTTTATTCTTTTCC | 23092 |
| rs148006491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961053 | TATCTTCTGTACAGC[C/T]TACTATGTTTTCTTG | 23092 |
| rs148027867 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873300 | ACTCAGGAACAAATC[C/T]GCCTCCTAAGATATT | 23092 |
| rs148034109 | in-del | -/TCGG | 0.230896 | 0.249269 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090452 | TCTACGATAGCTATC[-/TCGG]TCAGTCGTGTCATTA | 23092 |
| rs148049304 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813217 | GAGTGCGGGGATTAC[A/G]GGCGTGAGCCACCAA | 23092 |
| rs148054764 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103018 | GGGATCTGACATCTC[C/G]CAACTATTTTTCTTC | 23092 |
| rs148055592 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129343 | ACTGAATGTCAAACT[G/T]TATTAGGCGTGTCAG | 23092 |
| rs148057250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026897 | GGATCAAGGTATTAG[C/T]AATGGATATGGTGAA | 23092 |
| rs148071726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911755 | TTTCAAAGTGGAAGC[A/T]GGTCCATAGCCATTA | 23092 |
| rs148075357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083205 | TACATTATTAGGCCA[C/T]GGATCACTTCCTCTG | 23092 |
| rs148076523 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005101 | TAAAAAAAAAATTAC[C/T]ACAACCCTTGTCTGT | 23092 |
| rs148083189 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835303 | AACCCATCAGAGATA[G/T]AATTTATGGTATAGA | 23092 |
| rs148085229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805621 | CGAAAAATGAGTTTA[C/T]ATGAAGGCCCAAAAG | 23092 |
| rs148092916 | snp | A/T | 0.125874 | 0.217008 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793744 | AGATGTGCGCCACCA[A/T]GCCTAGCTAATTTTT | 23092 |
| rs148101173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846933 | GCTAAGGACTTTTCA[C/T]GTCTTATCTCAGAAC | 23092 |
| rs148105567 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217379 | CCCTGGCCAATCTAC[G/T]GGGAAACTGTCCATT | 23092 |
| rs148107684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132284 | TTTTGTTTCCTACAC[A/G]TCGGCTTTTGAGTTC | 23092 |
| rs148110734 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061959 | TGGTCCAGAGCAGTC[A/G]TTGAGGACCACCATG | 23092 |
| rs148114388 | in-del | -/T | 0.105214 | 0.203807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790368 | CTCTGCTGGATAGTA[-/T]TTTTTTCCCATCGTA | 23092 |
| rs148116848 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186687 | ACAGGTAATTTGATA[C/T]CTGTGGACCTATTTG | 23092 |
| rs148129381 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080308 | CCTACTCCGGATTTA[C/T]GACCTGTGAATACAG | 23092 |
| rs148135077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896898 | TATCCATGTGAGGTG[C/T]TTAGAACAGAACCTG | 23092 |
| rs148144867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860614 | AGGCTTCAGAATAAG[A/G]AGACATGATTGAGAA | 23092 |
| rs148146633 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788331 | TTAAAACCAGCTCCC[A/G]TTTCTCTGCTTGCTT | 23092 |
| rs148150108 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229235 | ATATTAAACAATTGA[A/G]CCCGAAGAGTCATAG | 23092 |
| rs148150772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146480 | GGCCACATAGCCAGT[C/T]AGGGCTTGAAGAGAA | 23092 |
| rs148167758 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182242 | CTGGAGGAACACAAA[A/G]CACTCGGCTTTGGTG | 23092 |
| rs148176817 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014477 | GGAGAGCCTTATCCT[C/G]TGGGAAAGCCAAAGT | 23092 |
| rs148182653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107283 | GGCAGGGGCTGGATC[A/G]TATAGGCCACGATGA | 23092 |
| rs148194198 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965371 | CGGTCTGCTAAGTAG[A/C]GGGTATTGTTCCTTG | 23092 |
| rs148209244 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783776 | TGATCCCAGGGTGTC[A/G]CCACCAGGAAATTAG | 23092 |
| rs148220089 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996454 | GCCAAGATCACGCCA[C/T]TGCACTCCAACCTGG | 23092 |
| rs148242079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840157 | ACTGTTGCTAAATAG[A/G]TTCATTCAAGGACTG | 23092 |
| rs148259581 | in-del | -/AGC | 0.0376037 | 0.131863 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779179 | GAGAACAACAGCATT[-/AGC]AGCCAGAGGAATTTT | 23092 |
| rs148259938 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851674 | TCCTTTAGGCCCTAT[A/G]TGGCCGCCCCCTCCC | 23092 |
| rs148262898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777882 | TAGAGTTTTATTCTA[A/G]GTGTGATGGGCAGCC | 23092 |
| rs148264362 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162865 | ATTCCAGGGTACAGT[G/T]GCCCACACCTGTAAT | 23092 |
| rs148265842 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220933 | GTAGCAGTGTCGGAG[A/C/T]GGAAATGCTTTTCTA | 23092 |
| rs148270895 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068071 | TGGGAGGCTGAGGTA[C/T]GAGAATCGCTTGAGC | 23092 |
| rs148277580 | snp | C/T | 0.000659391 | 0.0181455 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143121099 | AGCCATCATGGACAT[C/T]AAATTTCAGAACATT | 23092 |
| rs148285049 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877975 | ACAAAATCAAACAAA[G/T]TAACACCGCAACACT | 23092 |
| rs148286589 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042785 | GAAATCTCTTCTCTC[A/G]TGTTGGCCAGAATGA | 23092 |
| rs148292431 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941202 | CTGCTTTCCACAATG[A/G]TTGAACTAATTTACA | 23092 |
| rs148293646 | snp | C/T | 0.0532157 | 0.154195 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869299 | GCAGCCTCAGCCTCC[C/T]GGGTTCACGCGATTC | 23092 |
| rs148299486 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839367 | ACAATCCTTTGAAGG[G/T]TTTTTTTTTTATTTC | 23092 |
| rs148302443 | in-del | -/TCAAGACCAGTCTGGAGGC | 0.0937726 | 0.195174 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876572 | CTTGAGCCTGGGAGT[-/TCAAGACCAGTCTGGAGGC]AACATAGTGAGACCC | 23092 |
| rs148303139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831453 | TTAGGTTTTATCAGC[C/T]GTCTGATTTACGTCT | 23092 |
| rs148314809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809768 | TCCATCCATCCAATC[A/G]CTCATTCATTCATTC | 23092 |
| rs148315650 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189766 | CTTTGATATTTTTCT[C/T]CTCCACCAGCCTGTG | 23092 |
| rs148323475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098067 | ACAGAAGAACTCTTC[C/T]TTTATAATAGCGCTG | 23092 |
| rs148325125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154424 | ATCATCTTTTACTTA[C/T]GTATTTTAGTACTGT | 23092 |
| rs148330981 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086393 | TGCCAGCACACTTGG[A/T]TGGGTTCCTGAAGAG | 23092 |
| rs148333076 | snp | A/C | 0.000785854 | 0.0198068 | intron-variant, synonymous-codon | ARHGAP26 | GRCh38.p7 | 5:143057907 | TGTTCATTGCAGTGG[A/C]GAACAGCAGCAAATG | 23092 |
| rs148340977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038528 | TATGGGCCAGATTGA[A/G]CCATAAGGATGTTTA | 23092 |
| rs148341755 | snp | A/T | 0.0505692 | 0.150756 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008765 | ACTTATGTCTTTAAT[A/T]TCTACATTTGAAAAA | 23092 |
| rs148353482 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893295 | CCCCTTTCTTAGCCT[C/T]TGATAACTCTCATTC | 23092 |
| rs148356479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823942 | AAAACTGAAAAGATC[C/T]TTTCTTTCAGTGGTT | 23092 |
| rs148362059 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112792 | ATATGCTAGAATTCC[C/T]TTCCTGTTTAAGGCT | 23092 |
| rs148377618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150107 | TACCTGTGCCAGGGC[A/G]AGGCTGCTGGGTTTA | 23092 |
| rs148398627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807659 | TTTGTTGATACATTC[C/T]CAGAATGTTCAAGTT | 23092 |
| rs148400250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188100 | TATTAATTCAGTGGA[A/T]AAGAAGCTTACACAT | 23092 |
| rs148404340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868058 | TATAGAATGTACTAG[C/T]TGGGGAGGCATTACT | 23092 |
| rs148416930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218884 | CTTGGTCTCTGATTC[A/G]TTTTCATTGTCTACC | 23092 |
| rs148420900 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134748 | ACTGACCCCTAAAAT[A/G]TACAGTATTGTTTCA | 23092 |
| rs148429010 | in-del | -/CTGCGCCAGCCATTGTGG | 0.0463947 | 0.145069 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194873 | TTCCTCCATGGCAGC[-/CTGCGCCAGCCATTGTGG]AGGGCCAGCGGGAAC | 23092 |
| rs148435767 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020239 | AGGCATGAGCCACCA[C/T]GCCCAGCCTTCTGGG | 23092 |
| rs148437981 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917453 | AATCTGGGAAGTGCT[A/G]TTGGCACCCTGTCAG | 23092 |
| rs148444203 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979065 | GCAATTATACAAAGA[A/C]CTTTTTGAGGCCATT | 23092 |
| rs148451458 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804291 | ATAACTTGCTATTCC[A/G]TAACTATTACACATA | 23092 |
| rs148453610 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183793 | TGAGTCCTGTGGCTC[A/C]TCAGCAGTGTCTCTG | 23092 |
| rs148463270 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148038 | TCCCTCATGGTTTCA[A/G]CCCCACATTGCTTCA | 23092 |
| rs148468470 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081588 | CTACCATCCGAAGAC[A/G]GTGAAAACAGAGGTG | 23092 |
| rs148487036 | snp | C/T | 0.252421 | 0.249988 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092272 | AGGTTCACGCCATTC[C/T]CCTGCCTCGGCCTCC | 23092 |
| rs148495379 | in-del | -/AGAA | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060921 | GCGAATATTAGAATT[-/AGAA]AGAAGAAGCTCAAAG | 23092 |
| rs148509257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890624 | GAAGACAGAGAGACC[A/G]GTTAGGAGAGAAGTG | 23092 |
| rs148514657 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175821 | TTCCTCATCTGAAAT[A/G]TGGCACAATAGGCCA | 23092 |
| rs148529611 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077627 | GCTTAAGCAGGTCAC[C/T]GTGGCTATGGGGTGC | 23092 |
| rs148529797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997822 | CAGATGTAATGCTGA[C/T]ATCGTGTCTAAGTGA | 23092 |
| rs148543665 | snp | A/C/G/T | 0.000164832 | 0.00907709 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142902001 | CTGGCCAAGGATTTC[A/C/G/T]GGGACTTCAAGACAC | 23092 |
| rs148546503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785256 | TCTCCTATCTGCTTC[A/G]TCTCTTGATCTTGTG | 23092 |
| rs148573344 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780575 | TTCCAGTTTGTGTGT[A/G]TTGTTAATTCTGGGA | 23092 |
| rs148582068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070202 | TCTTGCCATTTTGCT[A/G]CTTTAAGAACTACAT | 23092 |
| rs148585562 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968131 | CATCATCCCTTTTAT[C/T]ATTAGCTCATTTAAT | 23092 |
| rs148589516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024664 | TGCTTGATATACGTT[A/G]TGTCATTTGATCCTC | 23092 |
| rs148592957 | snp | C/T | 3.29473e-05 | 0.00405864 | missense, intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207254 | GGCCCATGTTCTCGG[C/T]GCCATCCAGCCCTAT | 23092 |
| rs148593422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953890 | ACTTCCCACAGAACC[G/T]TGGTTGACATCGTCC | 23092 |
| rs148596465 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853299 | AAGTGATCCCCCTAC[C/T]CCTACCTCTGCCTCC | 23092 |
| rs148600795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943331 | AAACTGGGTAGTATA[A/G]AAATATGTATTTATT | 23092 |
| rs148604145 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870482 | AGGATCTCAGTTCAC[A/G]GGACTTAAGTCACAG | 23092 |
| rs148610029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156624 | ATAGTGCATAGTGAT[C/T]TAGTGCGTTAAGCTC | 23092 |
| rs148611502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216355 | TGATCTTTGAAAAAC[A/G]GAAATGGCATTAAAG | 23092 |
| rs148618759 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176421 | GCAGGCTTGGCAGGC[-/G]GAACCCTTTGGGCAG | 23092 |
| rs148619231 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118725 | TGCAGTGATCTATGA[C/T]CATGCCACTGCACTC | 23092 |
| rs148628594 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143166534 | TTCTTTCCCACCATT[C/T]TGTGCCTGGGCTTTA | 23092 |
| rs148642255 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060490 | CTCCAAACCTCTAAA[A/G]CAAATGATTACCAGG | 23092 |
| rs148650832 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811469 | TGGCTTCCAATCCTG[G/T]CCTGTCCGTCACGTG | 23092 |
| rs148651628 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011465 | CCCCAGCACCTGGAA[C/T]GTTGCCTGACCATTA | 23092 |
| rs148655831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939051 | AAAAATAGCCAGATA[C/T]TGGCAATTTCTTATG | 23092 |
| rs148663880 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210379 | TCAATCATCTCCCAC[C/T]GAGTCTCTCCCACAA | 23092 |
| rs148664792 | snp | A/G/T | 0.00835572 | 0.0641442 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895121 | CAATTTAAAACTCTC[A/G/T]CAGACCATGGATTTT | 23092 |
| rs148667624 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826016 | ACCTAGATTTTCTTA[C/T]CGATTTGCTGGTTAA | 23092 |
| rs148673495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179893 | CCAAGGTTACCATGA[C/T]CTCCCTGTCAAACCT | 23092 |
| rs148675969 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113881 | AGAATGCCTTTTTAG[C/T]GTAGGTTGGACTTGC | 23092 |
| rs148718156 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930402 | GAGAATGAGAATTTC[A/T]GAGAAGAGGAGGGAG | 23092 |
| rs148719126 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857082 | TCACTTCAGTTTCTC[C/T]CTCCATCTTCACAGG | 23092 |
| rs148725117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143625 | AAACTACCCCTTTCT[A/G]TTCCAGCAGCATAAA | 23092 |
| rs148735327 | in-del | -/CCCCC | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227494 | CGGCTGGGTGCTGAA[-/CCCCC]CCGCCTCTCTGTAAT | 23092 |
| rs148737125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035408 | CTGGATGAGACTGGA[A/G]ACTATTATTCTAAGT | 23092 |
| rs148774469 | in-del | -/TC | 0.102014 | 0.201495 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898618 | ACACGTCAGTCTGAT[-/TC]TCTCTCTCTCTCTCT | 23092 |
| rs148788711 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105232 | AATACAAAAAATTAG[C/G]TAGGCATGGTGGCAC | 23092 |
| rs148793078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030045 | TATATATATGTGTCC[A/G]TCAGTCAACTTATAG | 23092 |
| rs148795750 | in-del | -/TT | 0.494526 | 0.0520291 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027176 | TCATGATTTTTTGTG[-/TT]TTTTTTTTTTTTGAG | 23092 |
| rs148804416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913355 | CTATATCTTACTTTT[C/T]CTTTCCAGTCAAACC | 23092 |
| rs148809453 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815120 | ATTCCCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 23092 |
| rs148826723 | in-del | -/C | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966572 | TAAAACCCTTCAGAA[-/C]CAGCCATATAGCCAT | 23092 |
| rs148826923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796453 | CGCTGGTTAAAAGAG[A/G]TGATGTACTGCTATT | 23092 |
| rs148828812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177437 | ATCGAATGCCAAGAC[A/G]CTCAGTCATGGTTGA | 23092 |
| rs148835701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008335 | TTACTACAAATCTGT[C/T]GCCACTGACAGACAC | 23092 |
| rs148836304 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084922 | TGGTGGCGCGTGCCT[A/G]TAATCCCAGCTACTC | 23092 |
| rs148843291 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079573 | ACCAGCCTGGTATTG[C/T]CGGCCCCATACAAAC | 23092 |
| rs148890870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141608 | CATTTTGCTGTGAGT[C/G]ATGGTATAAAAGTAG | 23092 |
| rs148898677 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970056 | AACAGCCCACACCAG[C/G]GACTTTTTGTAGATA | 23092 |
| rs148907706 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821609 | TTTGTTAGAAATTCA[A/G]AATCTTGGGCCCCAT | 23092 |
| rs148911776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855595 | TCCTGCTGGCTGCCC[A/G]TTATGTACTAGACAC | 23092 |
| rs148913604 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782704 | ATTTGACCTTTGGAG[A/T]TGAAACTGGAGAAAA | 23092 |
| rs148916009 | snp | C/T | 8.36561e-05 | 0.00646692 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222401 | GGAGGGGACTCTGAA[C/T]GGAAAGACTGGCCTC | 23092 |
| rs148917437 | snp | A/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945047 | CAGGCTGTGTGATTC[A/G/T]ACAGGGAACCCACTG | 23092 |
| rs148918918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871976 | TCACAGCGTGTGGGA[A/G]GGCAGTCCAGGAGCA | 23092 |
| rs148920414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846185 | GAGTTATATGCCAGA[C/T]GCTGGCTTTGTGTAT | 23092 |
| rs148922970 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769567 | AAGTGCTCAATATCT[C/G]TTATTAAATGCCAGC | 23092 |
| rs148928036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157818 | TCACGTGAAAAGCAT[C/T]GGTAAGCTTTAGAAT | 23092 |
| rs148942315 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168725 | GCTATATCTCTAGGA[A/G]ATTAGCTCTAGGCTC | 23092 |
| rs148948523 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102633 | CATCCGGGCTCTAGG[A/G]AGACAGAGACTCTTT | 23092 |
| rs148960325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958095 | GGCCCCCAAACCTAT[A/G]TGGTCATTTTTGTCA | 23092 |
| rs148962481 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883783 | GAATCTCTGTGACTG[C/T]GCCCTGTTTATTTCC | 23092 |
| rs148968448 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940540 | CCACTTATAAGTGAG[A/T]ATATGGGATATCTGG | 23092 |
| rs148972231 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909994 | AGAGTTACTAGAAAG[C/T]ATGTCATTGGGTAGT | 23092 |
| rs148973363 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842806 | GCAATAGGCTTAGAA[C/T]GTAATTGTTTAATAA | 23092 |
| rs148979088 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127581 | CATGGATGACCCCCA[C/T]TTAACACCTGGACTA | 23092 |
| rs148983214 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801187 | GACTCTTTCCTCTGG[C/G]TTTGAGCTGTGGAAT | 23092 |
| rs148984850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181982 | CCTCCCTGGCTTGTA[C/T]GCTCCTGTGCTTATT | 23092 |
| rs148990000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115525 | CTCTTGCCCCAAGCA[A/G]AAGCAGGCCACTAGG | 23092 |
| rs148993370 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013624 | TGTGAGACATTAGTT[A/T]ACCCCTCTAGGCTTC | 23092 |
| rs149009767 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056298 | GAATTTACAGCAGAG[G/T]ACAGAAACTTCAGAA | 23092 |
| rs149041792 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145330 | TTTAAGCTTCTCAAA[C/T]TAAAGTTAATACAAC | 23092 |
| rs149045754 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044619 | CGGGGTTAGTCCCTG[A/G]AACCCAGTGGACTGA | 23092 |
| rs149056881 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936523 | GATACAGACAAGCTT[C/G]TTCTAAAATTTATAT | 23092 |
| rs149057927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864349 | ATTTAAAAGGCACGA[C/G]TTGAGCTTAATAAAC | 23092 |
| rs149068187 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823338 | ATGCAGATTACAAAT[A/G]TTGGCTACCCCAGTG | 23092 |
| rs149079060 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777425 | TGTTATCACCATTGA[A/G]CTACTGGGGAAAGCA | 23092 |
| rs149089090 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203030 | GTCAAAGACTTCATG[A/G]CTAAAACACCAAAAG | 23092 |
| rs149103902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032207 | GGATATTTGGTGCAA[A/G]CTCTGCCAGCATTCA | 23092 |
| rs149108727 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932306 | GCTTCTGTATAGATG[C/T]AGTTCTTGAGCTTTG | 23092 |
| rs149113595 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992378 | AACTGATTCGAAAGG[C/G/T]TCCAAGATGATTTAA | 23092 |
| rs149120056 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889353 | CACGGTGGCTCATGC[C/T]TGTAATCCCAGCACT | 23092 |
| rs149121597 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816873 | TGTCCAGTGTGGTTT[G/T]CATGGAGTGTGGAGG | 23092 |
| rs149125908 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905153 | AAGGTTTTAGGTCTA[C/T]TTGAAAATATAAATT | 23092 |
| rs149131124 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809602 | GGCTGTGAAAAGAGA[A/C]AAATAGTCCTCCTTT | 23092 |
| rs149156751 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135963 | TGGCCTCACTCACAC[A/C]TGCTGAATGAATGAG | 23092 |
| rs149163023 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964119 | AGACTGTCTGTTTCT[A/G]TATAGGATACCTGGC | 23092 |
| rs149176486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220721 | CCTGAAGCTTAGTGA[A/T]CTGAAATTGGCCAAC | 23092 |
| rs149179400 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981928 | TCTGCATTTTACTCT[C/G]TAATTTATTGACATA | 23092 |
| rs149182671 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875772 | GACAGAGAGGGTCTC[A/T]CTCTGTCACCCAGGC | 23092 |
| rs149184979 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804942 | AATGGAATCATTCAA[C/T]GTATGATTGTTTGTG | 23092 |
| rs149185901 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185812 | GGCAGAGTTGTCACA[A/T]GGCTGGCGAGCAGAG | 23092 |
| rs149188321 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161159 | TGGGATTACAGGCAC[A/G]CAGCACCACACCTGG | 23092 |
| rs149198894 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082992 | AAAGATTGTCACTGT[A/G]GAGTGACATTTTGCA | 23092 |
| rs149233842 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848437 | TGGTTTTCCCAGTCC[C/T]ATTTTCCTCCTTTAC | 23092 |
| rs149236241 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218508 | TGGGGACAGTCAGCC[A/G]TTAGAGACCTTAGTC | 23092 |
| rs149236592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772441 | TTTTGATTGAACCTC[A/G]GGCTGGCTTTAGTGA | 23092 |
| rs149239813 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134388 | CTGCTCCTACACAAT[A/G]AGAGCTGAGCTCAGG | 23092 |
| rs149244572 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065079 | ATTAAGGGAGGAGTG[A/G]GAGGAAGACACTCTG | 23092 |
| rs149254121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018994 | TATTCAGACCACCAG[C/T]GTTTTTTATTAGGAT | 23092 |
| rs149254927 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946577 | ATTCTCCAAAAACCA[C/G]AAAGTGGTAATATTT | 23092 |
| rs149266010 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000344 | CCTTTGGACCAGCTT[C/T]ATGATAGCTACAGAC | 23092 |
| rs149275746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960245 | CACCAAATAGTAATC[A/T]TGAGCCTAAATTGAC | 23092 |
| rs149276423 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885608 | GTAGCCTTCCCGCCT[G/T]TCAAGGTGGAAGACA | 23092 |
| rs149282474 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170276 | AACAGTGGCTCAGCA[G/T]CTCTGAGAGCTCCTC | 23092 |
| rs149286163 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911588 | TTTTTAAAGCAATCA[A/G]TAGTTGAACAGACCA | 23092 |
| rs149287289 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844459 | AGACTTTGAAATATG[A/G]TGAAAGTTCAGGACA | 23092 |
| rs149288099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215807 | GTCAGAACCTTCTTC[A/C]TTTTTATGTGCGATG | 23092 |
| rs149296580 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128657 | CACCACGCAGTCCTC[A/G]GTCCCATTGTCTGTC | 23092 |
| rs149298935 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183667 | AGTGGAAATTCCCCC[A/G]GGGCCTCCTCGGACG | 23092 |
| rs149301215 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117024 | AGGAAGCCTGTAGAA[C/T]TGGCAGTTCTTTCAA | 23092 |
| rs149306091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015149 | AAAAATGTTCCCCTC[C/T]ACCTCCAAAAAAAAT | 23092 |
| rs149328773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955279 | GCTCTCCAGACTGGG[C/T]GACAGAGTGAGACCC | 23092 |
| rs149336932 | in-del | -/AAAT/AAATAAAT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105378 | GAAGCTCCATCTCAA[-/AAAT/AAATAAAT]AAATAAATAAATAAA | 23092 |
| rs149359015 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120716 | TTCAAAGGTTAGTAA[C/T]TTGGCAGATAGTTGC | 23092 |
| rs149359747 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046389 | CTCTTAATACATTGG[A/G]GGACTTTGGGTTGGA | 23092 |
| rs149372057 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938680 | GCTATGGAAAAGATG[C/G]CTCAGGAAGCCAGGG | 23092 |
| rs149373384 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866773 | CCTCAGGAAAAGCAC[A/G]CAGATGTATGATCAG | 23092 |
| rs149394406 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779707 | AAATATGAACTGCCT[A/C]CTCCTCTGAGACTTC | 23092 |
| rs149403595 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143069950 | AGCTAGCACTTCCCA[A/G]AGGCCTGGGCTCCCT | 23092 |
| rs149420699 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108539 | TTTGGTAGACTGGCC[C/T]TTGAAATAAAGCTAA | 23092 |
| rs149423081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005013 | ACAGTTTCTCGTTCA[A/C]CTTTGTTGCACATTT | 23092 |
| rs149425002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933951 | CTCAGTTCATTTTTA[C/T]AGTACTTTCACTCAC | 23092 |
| rs149430716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834625 | CAGGGCCCCTCCCCA[C/T]GTAGTCTTTCATCCT | 23092 |
| rs149435298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890526 | GAAGTCCTTGAAGGG[A/G]ACCATGAGACCATCT | 23092 |
| rs149438300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820249 | GAATTCAGTTCTGAG[C/T]CATCCCAACTTCTTA | 23092 |
| rs149441320 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174962 | AGAGATAAGGAAGCT[G/T]AAGTGTAAATCTGTG | 23092 |
| rs149447938 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811443 | AGTGTGGGCTCTGGA[C/T]GCCGACAGCATGGCT | 23092 |
| rs149456157 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024048 | GCCTGTGCAACACAG[A/C/T]TGCTGTGGTGCATTG | 23092 |
| rs149456793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099854 | GTTTCAAAAATAAAA[A/G]CAATAATAAGGGATT | 23092 |
| rs149466388 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987796 | TATATGCTGGATTAC[A/G]TTTATTGATTTGTGT | 23092 |
| rs149473573 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137683 | TTCATTGATGCACTT[G/T]CAAGTTAATGTTTAT | 23092 |
| rs149474514 | in-del | -/AAAATAGCCAT | 0.287867 | 0.247116 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202474 | AGAATCAGTATCATG[-/AAAATAGCCAT]AAAATAGCCATACTG | 23092 |
| rs149475501 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118017 | TAGGGATGACAACAC[-/TG]TGTAATAAATGCAGG | 23092 |
| rs149476981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038182 | GCCTACCAGCCCTTT[C/T]TAAGTAGTGGAAAGA | 23092 |
| rs149477577 | snp | A/C | 0.0256215 | 0.110247 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967187 | AAGTAAGATTCAGGG[A/C]AGGGAAAACAGAACG | 23092 |
| rs149487547 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921302 | TGTCTCAGGTGATTT[G/T]CTTCCAGAGGCAGAA | 23092 |
| rs149494206 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201872 | AAATAAACAAAAGGC[A/T]TAATTCCTTTAGTCA | 23092 |
| rs149499176 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877903 | AGAGACTTGCAGATG[G/T]TTTGTGGAGAAGACT | 23092 |
| rs149501375 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806639 | TTATTGTGTAGTGTG[G/T]GCATCTAGAGTGATG | 23092 |
| rs149506925 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095664 | ACCTCCACCTCCCAG[C/G]TGGGTTCAAGCAGTT | 23092 |
| rs149512674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210351 | CAGTACAGGAAAGAC[C/T]GTCCCCAGTGATTCA | 23092 |
| rs149515320 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152241 | TTTAATAATAATGAA[C/G]CAATATAAATATTGG | 23092 |
| rs149521420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982680 | TATACCTTTCTTCTT[G/T]AGAGGTTTTGAAATG | 23092 |
| rs149536983 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951024 | TTCCCTTTCCCTTTC[C/T]CTTTCCCTTTCCCTT | 23092 |
| rs149542620 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915707 | GACCGTCCTAGGAAA[C/T]ACCTCCTCTCAGTTT | 23092 |
| rs149547791 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196971 | AATGAGGATAGACTG[C/T]ATATATCCCTAAATG | 23092 |
| rs149563364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798352 | GATGCAGCATTCCTC[C/T]GCTTCCCTTCACCTC | 23092 |
| rs149568283 | snp | A/C | 0.0962929 | 0.197165 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179022 | TTACAGGCACCTGCC[A/C]CCACACCTGGCTAAT | 23092 |
| rs149584316 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898704 | TGAATTAATCTTCAC[C/T]GCAACTCTGTGCAAT | 23092 |
| rs149588542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803788 | CTGTGGAGGAGTCCA[G/T]CAGTGAACATCCCAT | 23092 |
| rs149604271 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814993 | ACATCATATTACTTA[C/T]GGAATTACATGATTT | 23092 |
| rs149628408 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075765 | GTGCAGTGGCGTGAT[A/C]TGAGCTAACTACAAC | 23092 |
| rs149629424 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143257 | AGACGTGTGAATTTG[C/G]CTTGGCTCTGTGAGT | 23092 |
| rs149634866 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971844 | AGGAAGCTGACATTA[A/G]GGATGAGGTTGATTT | 23092 |
| rs149638117 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869032 | CAAATACAAGGTGAT[A/G]AGGCACAGAGAGTAA | 23092 |
| rs149644778 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127203 | AGGCTACTTAGTGTA[-/TG]TGTGTGTGTGTCCCC | 23092 |
| rs149667758 | in-del | -/A | 0.0298908 | 0.118541 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821144 | CTTTTATTATCCCCT[-/A]TCTTTAAGGCATCTT | 23092 |
| rs149671565 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048471 | TCATCATGTTGCCCA[A/G]GCTGGTCTCAAACTC | 23092 |
| rs149672739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122030 | ATGTTGTAAGCCACC[A/G]CTACCTCTTGTCTGA | 23092 |
| rs149675399 | snp | A/G | 3.3066e-05 | 0.00406595 | synonymous-codon, nc-transcript-variant, intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037200 | TGCTCTTTCAGCTGC[A/G]CAGTTGGACAGCATT | 23092 |
| rs149683236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940301 | CTCAGTCCTTTCTGA[A/G]CTTTCTTTTTATTTA | 23092 |
| rs149689187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842302 | CGGCATGTTTCTTGA[A/T]ATTGTTCTTGAAAAG | 23092 |
| rs149709838 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986881 | CTCTGTTTTGGTACC[A/T]GTACCATGCTGTTTG | 23092 |
| rs149734129 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007587 | GTTGTATGAAGTTGT[C/G]GCTGAGTACAGACTC | 23092 |
| rs149738499 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935333 | TTAAAAACATGGGTC[A/T]GTAACCTTTTTCTGT | 23092 |
| rs149739096 | snp | A/G | 0.00158008 | 0.0280632 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903521 | TTCTTTGATTTGAAT[A/G]AAATTATTTTCATCC | 23092 |
| rs149742656 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836760 | CACCCTTCCCAATTT[A/G]GAAAACCTTTGGATC | 23092 |
| rs149743186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208466 | CCCCATGCTATTTAT[A/G]TATATACAGATACAT | 23092 |
| rs149747287 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891237 | GGTGGTGGTGAGAAG[C/T]AGGACCTTCTGAAAC | 23092 |
| rs149749529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822263 | AGAGTGCTGCCTGAT[A/G]ACTCAGACTCACAGT | 23092 |
| rs149752249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795652 | CCACTTTTTCATTAC[A/G]TTACAATTTATCGCC | 23092 |
| rs149752843 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177204 | ATAACACTTCATCAT[A/G]TTAGTTTCCCAAGTG | 23092 |
| rs149755502 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111190 | TTGCTTTCAAATTAT[C/T]CTTGTAAAAATAATC | 23092 |
| rs149759843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812025 | CCTAGCTGCTGTGAT[A/G]AGTTGGCATTCTCAT | 23092 |
| rs149765477 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102353 | AGAAATGCCACCTCC[A/G]TTTCTTTCAGAGGTT | 23092 |
| rs149770980 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997417 | TTTTTCTTTTCTTGA[A/G]GGGTTGGTGGGGACA | 23092 |
| rs149784345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883292 | ATAAGGCTGGTGGGA[A/G]CGGATACATGTGAGC | 23092 |
| rs149787444 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039382 | CCAGCTAATTTTTGT[A/G]CTTTTAGTAGAGATG | 23092 |
| rs149787626 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113467 | TATGGCCATAATTAT[C/T]TCCTTTTTGGACTAC | 23092 |
| rs149801277 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925118 | TAACTGCTGATCATG[A/C/G]CTTCCCGCATGCCAG | 23092 |
| rs149804938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825881 | TCGAATCTGCCTGTA[A/G]CAATGTTGCCTTTCC | 23092 |
| rs149808834 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140601 | TGACTAAGGAAATAT[C/G]CTTCCCTTTGGAGCC | 23092 |
| rs149820550 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163513 | TCGAGTGCAATGGTG[C/T]GATCTTGGCTCACTG | 23092 |
| rs149831000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055876 | GGTGAAATCTCAGAA[C/T]GCTTGCAATAGGGAA | 23092 |
| rs149832368 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985182 | AAATACAAAAAAAAC[G/T]TGTTGAATAAGGAAA | 23092 |
| rs149836026 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953674 | CCTGTATGGACAAGA[A/C]TGTCCTTTTATTCTT | 23092 |
| rs149838329 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879072 | GTAACTTAGACCCCA[C/G]TCTTTTACCAGTTCC | 23092 |
| rs149849380 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769315 | CTGGTTCCTAGACAT[A/G]GAGATAATTTATTCA | 23092 |
| rs149853395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994111 | GTCACCTTGCATTTC[A/G]GAGTGAAAAACATCA | 23092 |
| rs149863823 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912098 | CAGGAGAAACAGAAA[-/T]CCCTAACAAATTCCT | 23092 |
| rs149864179 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198665 | GAGAAAAGATTCGGA[C/T]TATTGACTTGGGGAA | 23092 |
| rs149869234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191420 | AATATATGCCACACT[G/T]TTACAAGAGGGTATA | 23092 |
| rs149879300 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156552 | AAGGAGGGCCCTGCA[A/G]TCTGTGTTTTACCAA | 23092 |
| rs149881415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181457 | CACCTTCCTCCTCCA[C/T]GCTCCCTAAACTTGA | 23092 |
| rs149882151 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087705 | GGCTGGAGTGCAATG[G/T]TGCGATCTCGGCTCA | 23092 |
| rs149891468 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906830 | CAGTCATGCCATACC[A/G]TTGATAATTATTAAA | 23092 |
| rs149895913 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980966 | AGTTGTCATTGTCGT[C/T]GTAGTGTCACACTTG | 23092 |
| rs149919795 | in-del | -/ACAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936109 | AGAAAATCCCAAGGA[-/ACAC]ACACACACACACACA | 23092 |
| rs149947103 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044403 | TCTGCAGTCCTTGGA[G/T]CCTGTGGTCACTGAG | 23092 |
| rs149947767 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974699 | TTTTCCTTCCATCCT[C/G/T]GCTTGTCTTCACATC | 23092 |
| rs149952949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870185 | TGGCATGCACCCAGC[A/G]CCAGTGCCAGCCTCT | 23092 |
| rs149955731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800702 | ATTTGTGCTTTGTTA[A/G]TAGACCTGCTTATGG | 23092 |
| rs149957787 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931315 | AAGGTCGTTTTTATG[C/G]CGCAGTCTCTTTTTC | 23092 |
| rs149969923 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144548 | GTACATGGGACCACA[G/T]GTGTGTACCACCAGG | 23092 |
| rs149972366 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775693 | TGTATGAATTTACCT[A/G]TTCTGTGTACTTCTT | 23092 |
| rs149996613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081190 | ATCAACCACAGGACT[C/G]ATGAGATCACTGAGG | 23092 |
| rs150001015 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001481 | TATGTGATAAGGCAA[A/G]TATAGCAAAATATGA | 23092 |
| rs150010853 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963283 | ATTTAGATTGATTCC[A/G]TGACTTTGCTATTGA | 23092 |
| rs150012311 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888432 | TTATGAGGGAACTGA[A/G]TTTCTCGTAGGGGTC | 23092 |
| rs150015411 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861952 | AATTCACGTTAGCTG[C/T]TGGTAGGAACAGTGC | 23092 |
| rs150017314 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790589 | ACAGTTCGGACACCT[C/T]ACCATGGTTCATGCG | 23092 |
| rs150021236 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172099 | GCTAAAACTGAGGCA[A/G]CATTTTCAAGAATGC | 23092 |
| rs150022846 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845844 | AGAGACCTGCCTCTA[C/G]TTCCTCCCCAAGCTC | 23092 |
| rs150028606 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216615 | CTATAGGTATTGTTG[A/G]GAGCAGGAGGAAAGT | 23092 |
| rs150032553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130309 | CAATTTTATTCCCCA[A/G]TAGCTTCCAGAAGGC | 23092 |
| rs150042087 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092833 | CTTGACTGAGTGCAA[A/G]CAGCTCCCACGTCTG | 23092 |
| rs150043900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016997 | TGGGTCTTGATTGTT[C/T]TGCAACACTCCTTCT | 23092 |
| rs150046234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913035 | GTAAGCTGCATGAGG[C/G]TTTGTCCTGGAAAGG | 23092 |
| rs150060149 | in-del | -/A | 0.326976 | 0.237854 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027538 | CTTACTGGTTTTAAA[-/A]CCAATTCATCCATTT | 23092 |
| rs150062135 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957332 | AGTCTTTGTGATTTC[A/G]TACACAGTTGAAATA | 23092 |
| rs150069646 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226860 | GAGCCATACTAGTGA[C/T]AAGGGCATCCCAAGG | 23092 |
| rs150078655 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103391 | GACAGTGTGGCAATT[C/G]TTCAAGGATCCAGAG | 23092 |
| rs150080241 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169788 | AGATGTCACTACACT[A/G]GACCTTTCTTATGGG | 23092 |
| rs150086010 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999884 | ATATATCTGACAAAG[A/G]ACATATCCAGAATGT | 23092 |
| rs150099240 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813699 | TAATCTTCTTTTCTT[A/G]TAAGGTCACCATATT | 23092 |
| rs150107960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868657 | GCGGCAGGGTGAATG[A/G]TGGTGCCCTTCGTTA | 23092 |
| rs150117523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829066 | AATAGGTTAGTAAGT[G/T]CTGGTTAGGCATGTG | 23092 |
| rs150123185 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204088 | AAAAAAAAATCACAG[A/T]AGTACTATGGAGTAT | 23092 |
| rs150127199 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115380 | AAGAAAAGACGTACT[A/G]TTATGATTTGGGGTT | 23092 |
| rs150128283 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224269 | AGGCAAAGCTGAAGA[A/G]AGTCAAGGTCACTGT | 23092 |
| rs150133671 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164889 | GACAGAAACCTAAGA[A/C]CCTCATCTAGAATCT | 23092 |
| rs150134277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071608 | AAAGCACAGTCAGTA[A/G]AAGCAAAAATAAATG | 23092 |
| rs150137869 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995683 | ATCCAAAGGATTACA[A/G]ATCATTCTACTATAA | 23092 |
| rs150142239 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143058107 | CAAGAACAAACAAAA[A/G]TATGTTGTGGGTTTA | 23092 |
| rs150147470 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954859 | ATACCTTTTACTGAG[A/G]TATTTGGTGTAGGGC | 23092 |
| rs150150241 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143214071 | TTTCGTTCACAGCAG[A/G]CACGGTCTTCGATAA | 23092 |
| rs150165417 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821389 | TGATGGCCCATAGTA[A/G]AGTTTGGAAATTTTG | 23092 |
| rs150165972 | in-del | -/A | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840180 | AGGACTGGGTAGTTT[-/A]TTGAGGTCCTTTATC | 23092 |
| rs150185264 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192807 | CCAAATTATCATTTT[G/T]CTTGGCTCTTCTTCC | 23092 |
| rs150194144 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090059 | AAATTCTTAAGCTCA[C/G]TGCATCCTTTCAGGT | 23092 |
| rs150195763 | in-del | -/ATAT | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963180 | ATATATGTATATATA[-/ATAT]TATATATATATATAT | 23092 |
| rs150200702 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989027 | TGGTGCAGAGCTGAG[A/T]TCAATTCCTGGATAT | 23092 |
| rs150201776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910399 | AGGTGATGTCTTCTC[A/G]ATTGTGTAGAGGAAT | 23092 |
| rs150213715 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805940 | TCTAGAGCATCAATT[C/T]CCTAATGTGGAAATC | 23092 |
| rs150244439 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933561 | CCATGCCTAGTAGGG[A/T]CATTCTGCTATCCTC | 23092 |
| rs150260775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976994 | GGCTCTTTCATTGGC[C/G]TGGGCCAGGTTCTGT | 23092 |
| rs150264066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871678 | CTGCCTTCCTGCCCA[C/T]GGTGTTCTGGCTTTT | 23092 |
| rs150289745 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137450 | GTCCTGGTTTGATGC[A/G]ACCTTACCTTTCTTC | 23092 |
| rs150307728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852230 | GAGCGGTCAGAGGTA[A/G]TTTAGAAGGGACAGA | 23092 |
| rs150316837 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900900 | TCAGCCTTCAGAAGC[C/T]GAAGTTAATGGGATA | 23092 |
| rs150333341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173939 | TTTTGGCAAAACTAA[A/G]TAGCTCCTCTTCCCA | 23092 |
| rs150334331 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082274 | GTTAGGAAAAATTCT[G/T]CTAGGATGAATGAAT | 23092 |
| rs150337198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816234 | GAGGGTAGGAACCAT[A/G]TCTTTTTTTGTTTAC | 23092 |
| rs150338067 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196624 | TTTCTCTATAAGGCA[C/T]ATTACAACCTTCTTG | 23092 |
| rs150340158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133195 | TTTTTAGCATGAACT[C/T]TTAGAAGAATAAAAG | 23092 |
| rs150350125 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095030 | AATAGACTCATGTCT[C/T]TTGGTTTTAATTCTG | 23092 |
| rs150353653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018279 | GTTTAAATATGTTCT[C/T]ATCTTGTCATCTGTC | 23092 |
| rs150359604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915120 | GGCGATTAAAGCTCA[C/T]TGTGGCACCTCCATC | 23092 |
| rs150380207 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227894 | AAAAATTTCACAGCT[A/G]ATATTTTTACAAAAG | 23092 |
| rs150387755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078772 | TGGTGAAATAAGACA[C/G]GTGGGTTTGATTGGC | 23092 |
| rs150405728 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123621 | TTTTGGGAGGCTAAG[A/G]TGGGAGGATCATTTG | 23092 |
| rs150408399 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022011 | ATTACCATCTAGACT[C/T]CTGTATTTATTTTGA | 23092 |
| rs150412231 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949601 | ATGTTCTAAACTCCA[G/T]CTACCATGTAGTTGA | 23092 |
| rs150423023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843770 | CTCTACCTTCTTTCC[C/T]TCCACTTTTCCTTTT | 23092 |
| rs150441267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014849 | TTGCTGCAAGAGTAC[A/G]AAGGAAATCCTGTCA | 23092 |
| rs150458468 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185011 | TGGATTTTTACCCCT[A/G]TATTATTTACTATAG | 23092 |
| rs150470697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009081 | CTACTCTCCCCCCCT[A/G]GTGTTTATCGTCAGG | 23092 |
| rs150475542 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905073 | GTAGCTACTTCAGCT[A/G]TGTGTTTTGTATATG | 23092 |
| rs150476613 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838667 | CTGTATATAGTGGGG[C/T]TTATATATTATTGTT | 23092 |
| rs150486824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797332 | GTTTTTATAATTAGA[C/T]AGAATTGTGATCTGT | 23092 |
| rs150491475 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178496 | CTTCCCCTACCTACA[C/T]TTGCTAACATCTGCT | 23092 |
| rs150499446 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194956 | GAAGGAGCAGGGCCA[G/T]GTGTGGAAGATATAA | 23092 |
| rs150511315 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092375 | TTCACCATGTTAGCC[A/G]GGATGGTCTCGATCT | 23092 |
| rs150512268 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063815 | TCCTGCCACAAGTGC[C/G]CTCTTGCTTTCCTGA | 23092 |
| rs150513061 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990678 | GTTAGTTTTCCTTCT[A/G]ACAGTTAGGACTCTC | 23092 |
| rs150525986 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878965 | CCAGAGGTGTTTCTT[C/T]GTTTATTTGTTTTTA | 23092 |
| rs150528189 | snp | A/C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808051 | CCATCCTGGCTAATA[A/C/T]GGTGAAACCCCGTTT | 23092 |
| rs150534056 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096928 | AGAGAACATAATATC[A/C]TCATTCTAGCCACCT | 23092 |
| rs150564234 | in-del | -/TC | 0.251859 | 0.249993 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093497 | TCTTTACTATTTCTA[-/TC]TCTCTCTCTTTCTTT | 23092 |
| rs150576434 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945950 | TCTCATTTAACCTGG[A/C]ACAGTTAGAGGCTTG | 23092 |
| rs150579571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873891 | GCTGAGATGAGAACA[C/T]AGCCCAGTTTTCTTT | 23092 |
| rs150584008 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142771630 | AGAATGTACATATCC[C/T]AACTCTCTCCCTCTC | 23092 |
| rs150588959 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159792 | TGGGTGGGTGTAATA[A/T]CTGTAATATTTCTGG | 23092 |
| rs150589735 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836325 | CAGCTTTTTTCCCCG[A/G]TGATGAACCAGTCAT | 23092 |
| rs150600242 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048107 | ACCCACCTTGGCCTC[C/T]CAAAGTGCTGGGATT | 23092 |
| rs150601668 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979560 | TGATGGGGCCACATT[A/G]TCAATCCCTGCAGAA | 23092 |
| rs150607209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039072 | AGTGGGGAGAGGAGT[A/G]GTCATATTGCACAGG | 23092 |
| rs150611710 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968763 | TGAGGTCTGGCCATG[C/T]TAATGAGTTTAGGTG | 23092 |
| rs150614416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866009 | AGGTTCAGCTCAAAC[A/G]CTACTCCCTGTTCTT | 23092 |
| rs150621263 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924923 | GACAGGCATCCTTCA[A/T]TGTTGGTCTTAATGC | 23092 |
| rs150628399 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982564 | GCTGAATAGCGGAAG[G/T]AAGGAATCTGAAAAG | 23092 |
| rs150630518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902301 | TTTCAAATTTGTAGC[A/G]TCTGTAGCATTGGAG | 23092 |
| rs150639553 | snp | A/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187048 | CATTTAGTAAACACT[A/G/T]TATGCCAGGCTTTAA | 23092 |
| rs150643108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793776 | TATTTTAAGTAGATA[C/T]GGGGTTTCTCCATGT | 23092 |
| rs150645697 | snp | A/C | 0.0127132 | 0.078853 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887285 | AAGAGGATACCTTGC[A/C]TCAAAACCTTCTCTG | 23092 |
| rs150649118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083295 | TACATCGCAGTAACC[A/G]GCCTAATGATCAGTT | 23092 |
| rs150649655 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152060 | AGAAGATCAGTGATT[G/T]CCAGGGATTCTGGGG | 23092 |
| rs150655136 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134965 | AGATAACCAAGGATG[G/T]TTCATTCATGCAGCT | 23092 |
| rs150656264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198417 | TTGTGCCTGAAATGC[A/G]GTATTGGAAAAGATT | 23092 |
| rs150660351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108427 | AAACTTTTCTGGACA[C/T]CATACATTACTGTTT | 23092 |
| rs150661836 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034190 | GAAAACAGTTTGGCA[A/G]TTCCTCAAAAAGTTA | 23092 |
| rs150671218 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993512 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCGAA | 23092 |
| rs150677189 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818375 | CTTGTTTCTTGGTGC[C/T]GTGCCCATAGGTGTG | 23092 |
| rs150693216 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861056 | CCTCTCTCATTCTGT[A/G]GTGGTCTGCAGTGGC | 23092 |
| rs150699053 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229353 | AACCTCATGAACACA[A/G]GGATGGAATCATCAG | 23092 |
| rs150702076 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146731 | GTGGAGTCGTAAGGA[C/T]ATTGGTGGCTAAATA | 23092 |
| rs150708300 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221419 | CTATTCAAAATGACA[A/G]CAACCAAAAAAAAAA | 23092 |
| rs150713760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068209 | AAATTTATTGAAAGG[C/T]TCCTGGGTCAATCAC | 23092 |
| rs150723379 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023454 | CTATTTTTAAAAGAC[A/T]TCTAAAGCCTTCAGC | 23092 |
| rs150723987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951865 | TCACAACTTCCACCA[A/G]CTGGGTGGGTTACAA | 23092 |
| rs150735430 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845731 | CAGATAACTGGCGGC[C/G]CTGTCTTCTGGCTGG | 23092 |
| rs150746776 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176418 | CCTGCAGGCTTGGCA[-/G]GGCGAACCCTTTGGG | 23092 |
| rs150786480 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906179 | TGGACACATGTGGTG[A/T]CGACCTGCCCCTCAG | 23092 |
| rs150789138 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841099 | GCTTGATTTCCTTTC[C/T]TCATCTTACCCCACC | 23092 |
| rs150795236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125359 | TAGTACCTGCAAGTC[C/T]AGAAACACCCTCTCC | 23092 |
| rs150797121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190881 | TTGACTACTTATACA[C/T]GCCAGAACATGGGTG | 23092 |
| rs150805346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087511 | ACTGTGCTCCCCATA[C/T]CCTCTCCATTGCAGC | 23092 |
| rs150808242 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011827 | CTCCACCTAGACTTC[A/G]TGGTGACTTTTGCCC | 23092 |
| rs150813217 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171556 | GACACCTCCTTACTT[C/G]CCAAGTTTCAAACTT | 23092 |
| rs150818589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001387 | GTTCTGAAATGTTTA[A/G]AAGTGCTGATATCTG | 23092 |
| rs150823418 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898223 | ACATATACATATATA[C/T]GTATGTGCATATATA | 23092 |
| rs150830529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888283 | CAGTTTGCTTTTCTA[C/T]GTCTCTATCTGGGGA | 23092 |
| rs150835459 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790287 | GCTGAATGACCTTCC[A/G]TTCTGGGCCTATAGT | 23092 |
| rs150841026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942131 | GAGGATGACCAAAAT[C/T]GTTTCTTAGGGAATT | 23092 |
| rs150844966 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215377 | AGGGGCAGAATTGTT[G/T]TAAACTATCAAAAGT | 23092 |
| rs150848635 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154640 | TTAAGTGATCAGTGA[A/G]GAGGAGGAAGGAACT | 23092 |
| rs150852794 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831892 | GCTACCTACATAGCC[A/G]CTTGACTGACTCTTG | 23092 |
| rs150856375 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205443 | TGGGGATTTTGTTGG[A/G]ATTTAGAATATGTTG | 23092 |
| rs150857969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116249 | AAGTCTAAAATGCTC[C/T]GTAAGCCTAAGTTCC | 23092 |
| rs150862036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043031 | GTTGTAAGAAATAAT[A/G]TAGAGATCCTGTGTA | 23092 |
| rs150867367 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166619 | AGCCCCAGTGCTTTC[A/T]TAGCCTCATTCTCCT | 23092 |
| rs150874246 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996740 | CAGTTAGAAATGGAG[A/G]TCTGCTCCAAAGAAA | 23092 |
| rs150879080 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060525 | ATCCAAATCACAGAG[A/C]TGTTGGATTTGTTTC | 23092 |
| rs150887382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856619 | GAGTTCAGTCAACTG[C/T]GGATGGAGAATATTT | 23092 |
| rs150888121 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225927 | TAGGAAGGAACTTGA[A/G]GACTAAAGATTTTAC | 23092 |
| rs150890051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784118 | CCAGAGCTCAGTGTG[C/T]AAGGTCAGCAGACTA | 23092 |
| rs150912458 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112864 | CTGTTCATCCATCAG[C/T]AGACATTTGGGTTGC | 23092 |
| rs150913551 | in-del | -/TGTGTG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796055 | ACTAAGGTGTTTTTC[-/TGTGTG]TGTGTGTGTGTGTGT | 23092 |
| rs150928136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868272 | GAGTTGGGCATGCCC[C/T]GGGAACTGGCAGAGG | 23092 |
| rs150953521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188475 | GTAATAGTCCTTCCC[A/G]GAGGGGAGTCTCCCT | 23092 |
| rs150958830 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132862 | AAAGGAATCTGGGGT[A/T]AAAAAAAAAAAAAAA | 23092 |
| rs150963563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152789 | TAGCCTCCTTAAAGA[C/T]GACGGATTACTGGAG | 23092 |
| rs150970347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984522 | TGTAACATTTTGTAT[A/G]TAAGAAACAGATCTG | 23092 |
| rs150971605 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109827 | AGTCTACAGAGAGGA[A/T]GACTAATACTGTTAC | 23092 |
| rs150980450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935200 | CTCATCCGAATCTGG[A/G]AACTTACATAATATT | 23092 |
| rs150981773 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863263 | TTACAGGTGCCCACC[A/G]CCAAGCCCAGCTAAT | 23092 |
| rs150983877 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995159 | CAAAAAGCAAAATTG[G/T]CAAATGGGATCTAAT | 23092 |
| rs150988193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:142920048 | TCTTTAATGAAGCAG[C/T]ATTCTTGGGTGCTTT | 23092 |
| rs150991876 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821857 | CATCTTTGCCCCTTA[C/T]GTATTGGTGCTCAGC | 23092 |
| rs150996658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200089 | GGAATTGTATTCATT[C/T]GTACATCACTGAAAA | 23092 |
| rs151010910 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208423 | AATAATTTATGAAGC[C/T]GAGTTTCACTTTTAG | 23092 |
| rs151013576 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148747 | CCTTCTCAGGTTCTC[C/T]TATACCCACTTTCCT | 23092 |
| rs151023472 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140277 | CTCTTTGAATCACTG[A/T]TGGAGTTTGGAGCAC | 23092 |
| rs151026622 | in-del | -/GA | 0.124837 | 0.216412 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778028 | TGTAATAGTTGAGGT[-/GA]GAGATGATGGCACCG | 23092 |
| rs151037214 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024912 | AGAATTACTGAGTGT[C/G]TGATTTTGAGAAATT | 23092 |
| rs151044779 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853356 | TCACCACATCCAGCT[A/G]ATTTTTGTATTTTTA | 23092 |
| rs151051681 | in-del | -/A | 0.379354 | 0.213933 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200597 | GTAGTATAATTCTCC[-/A]AAAAAAAAGCGAGGA | 23092 |
| rs151089012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801772 | TGCAAGGAATAGGGA[C/T]GAAAGTACCTTGTCT | 23092 |
| rs151091728 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786655 | TCTGGAGTTCTAGAA[-/TT]TTTTTTTTTTTTTTT | 23092 |
| rs151096038 | in-del | -/TC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111317 | CCCTCTGTCTGTCAG[-/TC]TCTCTCTCTCTCTGC | 23092 |
| rs151107337 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811742 | TAGCACAATGCCTGG[C/T]GTGCAGCTATTACTT | 23092 |
| rs151111269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127934 | CCTGCTCAGGAAGCT[A/G]ATCTTGTCCTGTGGT | 23092 |
| rs151121130 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089560 | ATACAAACTCTTCCT[C/G]TTTTTGCTACTATCA | 23092 |
| rs151128902 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910048 | TATAAAAATTTTTTG[A/G]AACAAATCCTGACAC | 23092 |
| rs151130911 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082153 | GCTATTTATAACTTC[C/T]GTTTAGTATCTGTTG | 23092 |
| rs151133517 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003498 | AAACATTTAGATGCC[C/G]CATAGATCACTTCCC | 23092 |
| rs151139515 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900044 | GTTATTCTCAAGTCA[G/T]GGGTAGTGTCATGCC | 23092 |
| rs151142122 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833858 | TCTTTCTGAAACAAC[A/T]CAAAAATTTCAAACT | 23092 |
| rs151151808 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792159 | GGAACCACATCTCTT[G/T]TTCTTCCAGTAGATA | 23092 |
| rs151153991 | snp | C/T | 0.000214138 | 0.0103452 | synonymous-codon, intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207291 | CTCATCCACGTCCAG[C/T]GACTCATCCCCCGTC | 23092 |
| rs151165641 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216406 | GCTCTGAGAATTACT[C/T]ACAAGGCCCTCCAGG | 23092 |
| rs151172013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206849 | CTCGCTATAAGCTAG[C/T]CCTGCCTCAGAACAA | 23092 |
| rs151172914 | in-del | -/A | 0.0364509 | 0.129988 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785189 | CCACCTCGGCCTCCC[-/A]AAAGTGCCGGGATTC | 23092 |
| rs151180134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016658 | CAGTGAGCCAAGATC[A/G]TGCTATTGCACTCCA | 23092 |
| rs151181123 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943660 | CCACCTACCTTTAAG[A/G]ATATTTAGAAATCCA | 23092 |
| rs151187567 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078394 | CTGGATTTCAATTCG[A/G]ATTTTGGTTTTTTAT | 23092 |
| rs151189853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974339 | AGGGCTCTGGTTCTC[A/G]ATGGTGTATTATTGT | 23092 |
| rs151192833 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895222 | ATTTAAGAAAGGATA[A/C]TTTTCTTTTTTCTTT | 23092 |
| rs151198671 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958179 | CCCCATTTCTCCTCC[A/C]CCTGGTTTGGCACCC | 23092 |
| rs151202988 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227296 | GACTTTAAAAGGAAT[G/T]ACCTAGGTGTTCTGC | 23092 |
| rs151204802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785661 | GGGTTTCAGCTTTAA[A/C]CATTTTAGGGACTAT | 23092 |
| rs151228129 | in-del | -/TGTGTGTG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806474 | TTATAGGCAATGAAA[-/TGTGTGTG]TGTGTGTGTGTGTGT | 23092 |
| rs151228489 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180360 | CGATCTCTTGACCTC[A/G]TGATCTGCCCACCTC | 23092 |
| rs151251422 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991325 | AAAAGCGCAGTATTA[A/G]GGTGGGAGTGTCTCG | 23092 |
| rs151256888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815490 | TATATTTTGTGTTTT[A/G]TTATAAATCTAAGGT | 23092 |
| rs151270953 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164030 | AAGAGACTTTATCTT[C/T]AGGTTGTATTTGTTC | 23092 |
| rs151298456 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838250 | GCAAGAGAGTGAGAC[A/T]CCATCTAAAAGAAAA | 23092 |
| rs151314439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876277 | CTTCCCATGCTAACA[A/G]TTGGTAGTTCGAACA | 23092 |
| rs151316794 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220216 | GCTTTATTCTTTCTA[C/T]GTTTTTATTTTGGAG | 23092 |
| rs151318478 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775047 | GATATAAACATTTGC[A/G]TGCAGTTTATATGTG | 23092 |
| rs151320274 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161321 | CCGGCCTCAGATTTC[C/T]TATTAAAATTAGGGA | 23092 |
| rs151324789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066408 | TTCTGGAAAACCTAA[A/G]GTAATACAGTAATAG | 23092 |
| rs151329647 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123480 | TAAACTCCCTGCCAA[C/T]AGAACTTAACTTTAA | 23092 |
| rs151331335 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142913200 | TGTGTTCCCACTAGG[A/G]AGAAGATGAATCAGT | 23092 |
| rs151333331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050120 | TTGTTGGTGGGCAGA[A/G]GGCCACCACCTATCA | 23092 |
| rs151338316 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949575 | TCTTTGGCTCAAGAC[G/T]TTTCAGTACAATGTT | 23092 |
| rs180670923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217198 | AAAAGGGAGGGGCCC[A/G]TGGAGGGGAAAGTCT | 23092 |
| rs180672995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790016 | AAGGTCTTTATTAAT[C/G]CAGTCAACAAATGTT | 23092 |
| rs180682771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808627 | TGCTTTCCTTGTTAT[C/T]ACTTTGTGGAGCAGG | 23092 |
| rs180698615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159599 | TACCAACATCTAGGC[C/T]CCTTCCCTGGAGCCT | 23092 |
| rs180703745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200030 | GTCAAAATGCCCTTT[A/G]GAAAATTAAACATTG | 23092 |
| rs180708650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826128 | AGTGTTGAATCTGGG[A/T]ATTATTTTTCAAGGA | 23092 |
| rs180709567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181487 | ATGGGAGAACTCTCG[C/T]GTGTTAGGGAAGCAT | 23092 |
| rs180713589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837180 | TGGAGGCAAGAAGGC[C/T]TGGGATTAGGTTCCT | 23092 |
| rs180716376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819523 | CTGGAGTTTGCCAGA[A/G]TAGACAGCCTTCTGC | 23092 |
| rs180716413 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224954 | AAGCGAGACACTACC[A/G]TTGAATCAGGGAATG | 23092 |
| rs180719383 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779856 | GTGGGTCAGGGGTAG[A/G]CAATGAATATTAGTC | 23092 |
| rs180721134 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850149 | CCTCTCCTGCTCTGC[A/C]TATGGCTTGTCCCCT | 23092 |
| rs180724742 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143283 | TGAGTGCTTTCCTGG[C/T]CTCGCCTCTGGGTTC | 23092 |
| rs180729110 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122546 | AAGATGTTAATTGAC[G/T]TTTATTTGCGATTCT | 23092 |
| rs180729501 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151421 | CAATCATGTTCTTTG[C/G]TATTTACCCAAATGA | 23092 |
| rs180733296 | snp | G/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865532 | CTTTCCTTATCTCCT[G/T]GCTGACCAATGGTCT | 23092 |
| rs180734723 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886038 | GGAGCCATCGCAGCC[A/G]TGGAGCTGTGACCAT | 23092 |
| rs180738854 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104382 | TGCAGGTAGTGGCAC[A/G]CACCTGTAATCCCAG | 23092 |
| rs180741214 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905794 | CATTAAAAGTAATGG[C/G]TAAAATCGCAATTGA | 23092 |
| rs180741782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188401 | TTCTTGCTAATGTTA[A/G]GACTTGCCATTTTGT | 23092 |
| rs180748360 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859868 | TAGGGTTCCTGGGCC[A/G]TTCATGTTTCTTTGG | 23092 |
| rs180749335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167955 | CCCTTCACGATGAGA[A/G]ATAACAGAAACATAA | 23092 |
| rs180753299 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924039 | GCTAATTTTTTTGTA[C/T]TTTTAGTAGAGACGG | 23092 |
| rs180755549 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876743 | GATTGAACCATTGCA[C/T]TCCAGCCTGGGCAAC | 23092 |
| rs180759634 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895843 | TAAAAACAAAAAAAG[A/T]TTACAATCGGCTTTG | 23092 |
| rs180760991 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087958 | CTGGCCTATCCTGGC[C/G]CATTCTTTAGAAGAG | 23092 |
| rs180764256 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916080 | ATGTGGAAGTGAAAG[A/G]GGGGATGGTTATATT | 23092 |
| rs180766109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094544 | GCCACAAAAGGAATA[A/G]CACTTGAATATAAAA | 23092 |
| rs180766267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130986 | GAATAGCCCTATCAG[C/T]GGTCTTCAGGAGCCT | 23092 |
| rs180770455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065231 | CATTGGCCTTGGGAG[C/T]GTGTTCTTCATGAAA | 23092 |
| rs180777207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044182 | AAGACAATTCAGAAT[A/G]GTTTACAAGGAAAAA | 23092 |
| rs180782820 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112923 | CTACAATAAAAATGG[G/T]TGTACAAATACTTCT | 23092 |
| rs180869923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880657 | CCTGTTTTTCTGGAA[C/T]TGTGAGTCAATTCAG | 23092 |
| rs180880773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921483 | TAGTTGCTATTTAAA[C/T]TAAACTTTTAGCAGG | 23092 |
| rs180910183 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900753 | ATAATAAGTAATGTT[A/T]AACAGGTTAAAAAAA | 23092 |
| rs180913761 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961711 | GTCTATCCTCCTGTG[C/T]CCTTGATGTTTTCAG | 23092 |
| rs180936699 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940347 | CTTTTAGGTTCAGGG[A/G]TACATGTGCAGGTTT | 23092 |
| rs180949172 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221803 | ACTGGCATTACAGGC[A/G]TGAACCACCAGGCCC | 23092 |
| rs180970069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077825 | GACCACCTAGAGGGT[C/T]CGAAGGCCAAGAGTA | 23092 |
| rs180978443 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785899 | CCCACACACCCCCAT[A/C]ATTTGTTCACTGTGT | 23092 |
| rs180981790 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053865 | ACATATCTTGTTTTT[C/T]TTTATTTGACATTAT | 23092 |
| rs180981965 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032844 | GTGTGCATGCATGCA[C/T]ATGTGTGTGTGTGAA | 23092 |
| rs180983193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024325 | AATCTACCCTCTCTC[C/T]CAGCTAGCTTTAGAC | 23092 |
| rs180987075 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203106 | TAAAAAGCTTCTGCA[C/T]AGCAGAAGAAACTAT | 23092 |
| rs180988447 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813097 | TGCCGGCTACCATGC[C/T]CGGCTAACTTTTTTT | 23092 |
| rs180992742 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015251 | TTAATTAGGTAAGAT[C/T]GTTTTAGAACACTTG | 23092 |
| rs180993141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989957 | TTTTCTCGAGCAGTA[C/T]CTTTGTGGCTTTCTC | 23092 |
| rs180994863 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995585 | TAAATTAGTTCAACC[A/G]TTGTGGAAGACAGTG | 23092 |
| rs181001175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804582 | CTGCAACCTCTGCCT[C/T]CTGGGTTCAAGCAAT | 23092 |
| rs181003360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980285 | ACATATCACTAATTA[C/T]TCATTCTTCGATTGA | 23092 |
| rs181004070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772661 | TGGGGGAAGCATTAC[C/T]TCTGAGTCACACAGC | 23092 |
| rs181005429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830685 | GTTTTGTATTTTTTC[A/T]CCCAAGCAGTTCTTG | 23092 |
| rs181010053 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871043 | TCATCAGGATTCTCG[C/T]TCTACCCAGCTTTCC | 23092 |
| rs181010942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007440 | GAATTCCTGTTATGC[C/T]TAAATTGGGTGGAAA | 23092 |
| rs181031196 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794375 | GCTATAAATACAGAA[A/G]GAGGGGGGACAGAGG | 23092 |
| rs181071266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823609 | CATAAGCAAGTACTA[C/T]AAGAAAAAAAAAATC | 23092 |
| rs181077281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976129 | CCTAACACCCAAGTA[A/G]AGATATGGTATCATC | 23092 |
| rs181081227 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863145 | AGAAGGAGTCTTGCT[C/T]TGTCACACAGGCTGG | 23092 |
| rs181097871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000687 | ATACACCATGGAATA[C/T]TATGCAGCCATAAAA | 23092 |
| rs181107538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985654 | ATGCTATCCCTCCCC[C/G]CTCCCCCCCACCCTA | 23092 |
| rs181108113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809208 | TTATTTGTGTGTTTT[A/T]TCAGTCTTAGACATT | 23092 |
| rs181117646 | snp | G/T | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966067 | TGTAGCATGCAGAAT[G/T]GGAATGATTCTATAA | 23092 |
| rs181117918 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851701 | TCCCTCCCGTTTTAC[A/C]CTGGTCTCACCACCC | 23092 |
| rs181127343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826741 | TTTTCAGCCTTAAAG[A/C]CCAGGTCAGTCTGCT | 23092 |
| rs181141031 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866356 | CCACTCATTCCCTGC[A/G]TGATCTTGGGCACGT | 23092 |
| rs181144493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886623 | TGAAGATCTTGTGCC[C/T]GAGTAGGGAAAAAGA | 23092 |
| rs181147925 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906586 | TATGGGTTCCTCTTT[G/T]GTTCAGGAGGCTATA | 23092 |
| rs181159456 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924731 | TATTACATCAGAGCA[C/T]GCATAGTAGTGCAGA | 23092 |
| rs181193602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164242 | TTCTTTAAACCCTGA[A/G]TCAATGTAACCAGGA | 23092 |
| rs181196329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154756 | AACCTCTGAATCCCA[C/T]AGGGTACCTGATAAT | 23092 |
| rs181198614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147763 | GTTGTCTCGGTTTCC[C/T]TCCCCACTGACTATG | 23092 |
| rs181201614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136344 | CAGATGGTAGACAGG[A/G]GATGCAAAAGGAGAA | 23092 |
| rs181202498 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184694 | CCTCTTAGAGCTTTC[A/G]TTTCTTTTGGAGGGA | 23092 |
| rs181206397 | snp | A/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175019 | GGAGCTACAGGAAGG[A/G/T]TGCCAGAGAGAACCT | 23092 |
| rs181216469 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071757 | TACTACAAAAAAATT[A/G]GCCAGGCGTGGTGGC | 23092 |
| rs181226385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117286 | TGCTGGACCGGCTCC[A/G]CAGTGCTCTGCCAGC | 23092 |
| rs181232809 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109072 | TTTAACTAATTAAAG[A/T]TTGTTACAATGGTGA | 23092 |
| rs181233965 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127058 | TATTTATTACAAGGT[C/T]TTCCCTTTACTTAGT | 23092 |
| rs181241211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090681 | AATTACACTGGGTTA[A/G]CTGATGGGGGAGGGC | 23092 |
| rs181248117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042978 | GTTTTTGTAAAAATT[A/G]AACTTTTCATTTTGA | 23092 |
| rs181250253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081478 | TGTAATTGGAAATGG[C/T]ACAGTTTTGAAGAGT | 23092 |
| rs181251373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023129 | CACTCTCCCACAGGG[A/G]TTTGGCAACACAACA | 23092 |
| rs181253971 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050114 | GCTATGTTGTTGGTG[A/G]GCAGAGGGCCACCAC | 23092 |
| rs181255449 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097661 | CCGTCTCTACTAAAA[A/T]TACAAAAAAAATTAG | 23092 |
| rs181257737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935440 | AAAAGCTGCCATGGA[C/G]AATATGTAAATGAAT | 23092 |
| rs181260246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005996 | CCCAGTGGTACCATA[C/G]GCTTCAAAACTATTA | 23092 |
| rs181262055 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028241 | GCAATGTAGTCTGTG[C/T]TCAGTAAGTGTTAGC | 23092 |
| rs181264982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791165 | CTTACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 23092 |
| rs181266765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988913 | GCTTTACTTCCAACT[A/G]TGTGGTTAATTTTGG | 23092 |
| rs181269444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011998 | AGAAAAACCTATCAT[C/T]GCCCACATTTTATAG | 23092 |
| rs181270256 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037823 | GTTCACAGACACCCT[A/G]AATTTTCTCTGGCAG | 23092 |
| rs181272125 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970657 | TTGGCCAGGGTGTAA[C/T]AGACAGGGGAGCCAT | 23092 |
| rs181274273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955859 | CTGTCTCCATGTTGC[A/C]CTCTCAGAGTGAATC | 23092 |
| rs181275173 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992436 | TTATTTTATTTTATT[A/T]TTTATTTTTTTTTTT | 23092 |
| rs181282048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114427 | GGCAGTGAGGATTCC[C/G]CCCGCCATCCTCTGT | 23092 |
| rs181289829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946084 | CACTATCCTCCCTTC[A/G]TCTAGGTAATAATTC | 23092 |
| rs181293853 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094858 | GTAATGGGAATGAGT[C/T]GGGGTGGAGCAGGTA | 23092 |
| rs181300736 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055091 | CATTATTAAAGGTTG[G/T]GTTATTGACCAGCTG | 23092 |
| rs181303176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078170 | AATCATGTTACGCTA[A/C]CTCAATAAAAAATGA | 23092 |
| rs181305029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217385 | CCAATCTACTGGGAA[A/G]CTGTCCATTTCAACA | 23092 |
| rs181315237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057496 | TAGTCATGCTGGCCA[C/T]GCAGTATGCACACAA | 23092 |
| rs181322093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084691 | CTTTGGGAATAACCA[A/G]CTGCTTGTAGGGCAC | 23092 |
| rs181326600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016343 | AGTTGCTTGCCTTGG[A/G]TGTCTAATGATTCTT | 23092 |
| rs181329352 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778530 | CTTGAAGACCTTCCA[C/T]GTCAGTACATGCATG | 23092 |
| rs181337347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980443 | GCCCAGGCTGGAGTG[C/T]GGTGGTGCGATCTAG | 23092 |
| rs181360404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818590 | CTTTATTTATTAGCT[A/G]TATCACCTTGGAGAT | 23092 |
| rs181363962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018711 | GCTGTTTTTGTCCCA[A/G]TACCTCTCTGTTTTT | 23092 |
| rs181387265 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940842 | AGCACTTTGGGAAGC[A/C]GAGGTGGGCAGATAA | 23092 |
| rs181397011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102849 | TCACCTCCCTTGCTT[G/T]CTTTGTCCTTACAGC | 23092 |
| rs181400711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188834 | GTGAGGGTAACCTAG[A/G]AAAAGGAGGTGTAAT | 23092 |
| rs181404717 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033646 | CAGAGGGTAAAGAAA[C/T]AGCCTTTGTCTAGGG | 23092 |
| rs181408219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064175 | ACACCCTATCCCCCA[A/G]GGTGTGCCTTCTCCA | 23092 |
| rs181419350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152119 | CAGGGTATTTTTTTC[A/G]CGGTGAGACTATTCT | 23092 |
| rs181426961 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131570 | TAGAAGACACTGTTA[C/G]GTTGAAACACATCCT | 23092 |
| rs181433485 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168802 | TGGTGGGATTAATAA[C/G]GAGAGGATATAGATA | 23092 |
| rs181434199 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910476 | GGATGTGGTGGCTCA[C/T]GCCTGTTAATCCCAG | 23092 |
| rs181437215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880777 | TCCTCACCCCTACAA[C/T]ACACACACCCCTGAG | 23092 |
| rs181439099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863414 | GCCCGGCCTCAAGTG[A/G]GTTCTTTTAAGGCCG | 23092 |
| rs181441533 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226182 | TACTAACAAAATTTC[A/G]TAGCTAAAGAATGCC | 23092 |
| rs181441775 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928299 | AAGACAGATAAAACA[C/T]GGAGAACCACTTCTA | 23092 |
| rs181448187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995852 | AAAGAATGCATTCAT[G/T]TCCTTTGTAGGGACA | 23092 |
| rs181449166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951141 | CTCAGCTCACTGCAA[A/C]CTCCACCTCCCAGGT | 23092 |
| rs181451256 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901198 | TTAAGTATATGAAGC[C/T]GTGTGGTGAGCATTG | 23092 |
| rs181458917 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195135 | CATCAAAGTTCATCT[C/G]TCTTTCTCTCTCTGT | 23092 |
| rs181464162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176855 | ATTTTCAGCTCATAA[C/T]CTCAGAATCCGTAAA | 23092 |
| rs181469395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203523 | GTGTGGCGATTTTTC[A/C]AGGATCTAGAGCCAG | 23092 |
| rs181472686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184980 | GGAATTAATGAGAGG[C/T]CTATGCAACAGTGAG | 23092 |
| rs181472967 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798625 | CTGGAAGGGTGGTGA[G/T]GGTGCAAGTACACTT | 23092 |
| rs181475444 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165767 | TTTCTATCTTTATGT[A/G]CATGATGTGTATTAT | 23092 |
| rs181480239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212941 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 23092 |
| rs181499980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794760 | CAAAATGATGTATGA[C/G]AACTATTAAGTAATG | 23092 |
| rs181500735 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922065 | GCCTGCTAGGGTAAG[A/G]TTCCATTTTCAAACT | 23092 |
| rs181503094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831080 | AATTCCGATCACAAT[A/G]CCTGGCATGCACATA | 23092 |
| rs181514588 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137399 | TGCCGTTCATGTCAG[G/T]TTCCTGCTGTGCCCT | 23092 |
| rs181521370 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961929 | GTTAGACAAAAATGA[A/C]GACAGATCCATTTCC | 23092 |
| rs181526510 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871364 | GCTTTTCAGGTGTGT[C/G]CTGGGAGCTTTCCCG | 23092 |
| rs181531665 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098079 | TTCCTTTATAATAGC[C/G/T]CTGCCTCAATTTTGT | 23092 |
| rs181560928 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207597 | AAAAGGGACCATTTG[A/C]ATGAATCAGCATGGC | 23092 |
| rs181569218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906976 | TGCCTTCTTCCTTTA[A/G]TAGTGCTTTGTTTTC | 23092 |
| rs181574491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925473 | CATAAACAGACATGG[A/C]AAAGGTGTCATTCTC | 23092 |
| rs181580325 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946490 | CAAAAGAAAGTTCTT[A/G]TAAGAGTGAGACTTT | 23092 |
| rs181609405 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773550 | TCTAGATCCCGTAAA[G/T]GAGAAACATGCAGCA | 23092 |
| rs181614132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222224 | TAATAAGTGATTGTA[C/T]TCATTGTCCAAGCTT | 23092 |
| rs181623939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813981 | TTGGGTGTGGACTTG[G/T]TGGCCACCATTACTA | 23092 |
| rs181638571 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019152 | GAATGTCAGGAATCT[A/G]TATCAGTGACACCAG | 23092 |
| rs181645271 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001682 | GTGATGGAGGTGGGG[G/T]ACCCACACAGAGTGC | 23092 |
| rs181645507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048771 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGTGCAC | 23092 |
| rs181657414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966547 | TGTTGATTGTAGGTG[C/G]ATTTAATTGTTAAAA | 23092 |
| rs181661174 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855150 | AAGAGTGAAGTCACC[A/G]TTTTAGAACATAAAT | 23092 |
| rs181661640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190368 | TGAATAGTGCTGCAC[A/G]GGGCAGGGTGCTTGC | 23092 |
| rs181666008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155069 | GTTTCTCACCCACCT[C/T]CAAGCAGAAAAGATC | 23092 |
| rs181668885 | snp | A/C | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890935 | AGTCAATTCTGTTTT[A/C]CTTATAGGGATTTCC | 23092 |
| rs181676288 | snp | A/G | 0.0170251 | 0.090679 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226476 | ACAGAGCCAGACTCC[A/G]TCTCAAAGGAAAAAA | 23092 |
| rs181676659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208324 | TTGTAGAGCCCAGTT[A/G]TAAGCATCAGAAGCG | 23092 |
| rs181697710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117554 | TCCCACCCAAAAAAA[A/C]GTTTCCTAAGACTTA | 23092 |
| rs181705567 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081752 | GGAGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 23092 |
| rs181720988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799048 | GGTATACCTCGAAGA[C/G]ATAATGTGTTCCACA | 23092 |
| rs181728010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851796 | ACCTGGTGCTCTTTC[A/G]GCATGGCCTTCTCTT | 23092 |
| rs181730374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779176 | GGTGAGAACAACAGC[A/G]TTAGCAGCCAGAGGA | 23092 |
| rs181734330 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915265 | AGTGGGCTTGCGAGT[C/T]GATTGCTCCTGAGTT | 23092 |
| rs181742381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887556 | TCTGTATTTCAGTGG[A/G]TGTTTTCCATTATGC | 23092 |
| rs181745094 | snp | C/T | | | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859464 | GTATTTTTAATCTGC[C/T]CATGTTCTTCTAAAA | 23092 |
| rs181745215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835956 | TAGGAAATTCAGGTA[C/T]GCAGAGTTGAAGCAA | 23092 |
| rs181746949 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954198 | TATCTCATTCTTTCC[A/G]TGAAATATAAGAATG | 23092 |
| rs181762252 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876059 | TATTCTGATATAGTT[C/T]AGCATTAGCAGATAA | 23092 |
| rs181785575 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980106 | GACTTATATTGCCAT[G/T]GATTAGTTTCCCTGT | 23092 |
| rs181802116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216793 | AAGAAAACACCTCTC[A/G]GTGTTGACTGAGTTG | 23092 |
| rs181833641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122194 | GGCTTCCCATTTCAT[A/G]CATTTGCCCACATAG | 23092 |
| rs181835002 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142500 | TTTTAAGATTTTTTT[A/T]AAAAAAAAACATTGT | 23092 |
| rs181839007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143058996 | GGTGTCAAAGAATCC[C/T]GATGAAGCATGTTTA | 23092 |
| rs181841729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086257 | TAGAAAACTTCCAGT[C/T]CCCTCTGGCATTACT | 23092 |
| rs181844073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795327 | CTCAGAAAGTGTTGG[C/T]TCTTTGGAATGATAT | 23092 |
| rs181847265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103495 | AAGACACATGCACAC[A/G]TATGTTTATTGCAGC | 23092 |
| rs181848025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064604 | ATCTATTTAAAGGGA[C/T]ATTGCACAGAGCACA | 23092 |
| rs181857084 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862996 | GTGTGCCTTGCTGTA[G/T]GAATATCCAGTATAT | 23092 |
| rs181859701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169579 | TACAGGCTGAGCCTA[A/G]TTTCTGTTGGTCCAC | 23092 |
| rs181860453 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023850 | CACTCTGCCTCCCTC[C/T]CTTGCCTGCGTTCCT | 23092 |
| rs181861985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043560 | CTGGGATAAATGTCC[A/G]AGTGTGCAAATTGCT | 23092 |
| rs181863128 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814689 | TACAGGCTCCGGAGT[C/G]CCACTAACCCGCATT | 23092 |
| rs181871470 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855511 | ATCTGCCCATCATTA[C/T]TGACTGCCTGTTATG | 23092 |
| rs181873008 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880024 | GTTGGCAAATAATTT[A/T]AAAATATATATTACC | 23092 |
| rs181873684 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006421 | TAGTTACTGAACCCC[C/G]TTTATGTATAATTCT | 23092 |
| rs181876431 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831382 | TGCTCTTTGGTCTCC[C/T]TTTTTCTCCTTGTTG | 23092 |
| rs181876515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900212 | AAAGGAAAGGTATGG[G/T]TCTTCCTCTCAGAAA | 23092 |
| rs181876866 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126569 | GTTCTAAACTTGCAG[C/T]TCAGATAGTGTCACC | 23092 |
| rs181884886 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098553 | TGAATTATTTTATCT[A/G]GAAAAGAGAAAGACC | 23092 |
| rs181885944 | snp | C/T | 0.02016 | 0.0983543 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:142919958 | AGTGAGCTGAGATCG[C/T]GCCACCACACTCCAG | 23092 |
| rs181889810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146950 | CAATTTATGGTGCCA[C/T]AGTAGGGCCACTCTT | 23092 |
| rs181891309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060162 | CTTACCCTAGGCTAT[A/G]CCTGAGCTATTGTTC | 23092 |
| rs181891585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809917 | CTCTCATGGATCTTA[C/T]ATTGGACTGGTGCAG | 23092 |
| rs181893453 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940115 | GCCTCCTTTGCTATG[A/G/T]TGCATCCCAGGCCTA | 23092 |
| rs181894361 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081964 | GCAGTGAGCCGAGAT[A/C/T]GCGCCACTGCGCTCC | 23092 |
| rs181897126 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038852 | GGGCACACACCACCA[C/T]GTCCAGCTAATTTTT | 23092 |
| rs181899797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142959966 | CAACTATATGGGATT[A/G]GTCTGTTTTTGTATT | 23092 |
| rs181918171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895120 | TCAATTTAAAACTCT[C/T]GCAGACCATGGATTT | 23092 |
| rs181927221 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867165 | TGTTGTTTAAATTAG[C/T]TGCTTGGTCAAGGTG | 23092 |
| rs181928406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971220 | TATCACTGATCATTT[A/G]TAAGGGACTATGCTT | 23092 |
| rs181933179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995199 | GAGCTCCTGCACAGC[A/C]AAAGAAACTATCACT | 23092 |
| rs181938866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934437 | GTGTGCTTTTTAGTT[G/T]CCTAAAGAGAGAGAT | 23092 |
| rs181982441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975362 | GAAAGAAACCTTTCT[A/C]CCAGCTTCTTCCAGA | 23092 |
| rs181987197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774759 | CCTCCCCACTAACCC[C/T]GGGCAACCACTAATC | 23092 |
| rs181997574 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180955 | CACCTGTGTGTCTCC[C/G]TGTTTCCATGAATTC | 23092 |
| rs181999796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934658 | GCTCTTTCTCTAGTC[A/G]GTGTTAGTGTCGTTG | 23092 |
| rs182004773 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823210 | TCTGGCATGGAAGCT[C/G/T]GTGCTAAACACATGA | 23092 |
| rs182005052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955369 | CTGATTGCAGAAAAA[G/T]AGGTGTTTGAGAAAC | 23092 |
| rs182008776 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221251 | ATGTCACAAAAGTAG[A/G]TATATATTCTTTGGA | 23092 |
| rs182020028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152283 | TAACCAGTGTATCGC[A/G]TTAATGCAAGATGTT | 23092 |
| rs182027578 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163781 | TGATCCATCTTTTTT[C/T]TCTTGTTCTCCAGGA | 23092 |
| rs182031422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115051 | GAAAATAAGTACTAT[A/G]GCCAGGTGTAGTGGC | 23092 |
| rs182032891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118608 | AGACTCTGTCTCTAC[A/G]GAAAAATTTAAAAAC | 23092 |
| rs182035510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202825 | AAACAAGCAATGGGG[A/G]AAGGATTTCCTATTT | 23092 |
| rs182037025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184250 | CCATTAGGGGGTAGA[A/G]AATGCCTCTTTTGGA | 23092 |
| rs182049648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891308 | TTTCCCTGATTGGAA[A/G]TCTTAGAAAATGCCC | 23092 |
| rs182072304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928744 | GATGTAGCTGTGAAG[A/G]GTGGGTGAATTAATT | 23092 |
| rs182074438 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115638 | CATCAGCACTACCTC[A/G]ACAGCCACCATGACA | 23092 |
| rs182084479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095923 | AAAATCAGTCCTAGC[A/G]TATGCATATAGTCGG | 23092 |
| rs182086153 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038601 | TGTCTCAAAAATGGG[C/T]TAAATCAACAGTGGT | 23092 |
| rs182094389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145402 | TGAAGCCCAGGGAAC[C/T]GTCCTCACTCTCTCT | 23092 |
| rs182098251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055667 | AGCCGCTGGGAAGAT[C/G]AAGACTTGCAAATAT | 23092 |
| rs182103128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079642 | TAAATATATTTACCT[C/T]GTTCAGGTCTTGGAG | 23092 |
| rs182109472 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162093 | TTGGTAAATCCAAAG[C/G]TGAAGCACAAGAGAG | 23092 |
| rs182110620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034731 | GGGTAAACTTATGGT[A/G]TATGAAGTATATACC | 23092 |
| rs182111697 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017749 | GGTACACAGCACTTT[A/C/G]TATCTGTTTTTGTAG | 23092 |
| rs182119086 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769015 | CACCATGCTCCATTT[A/G]TGAATTTAATACATT | 23092 |
| rs182121256 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010910 | GGGATCAAGGATGGC[C/T]GAAGAAAAATACTTG | 23092 |
| rs182139651 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792242 | TTGCAGGATTTAATA[C/T]CAGTTCATTTGGATA | 23092 |
| rs182144507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974341 | GGCTCTGGTTCTCGA[C/T]GGTGTATTATTGTTC | 23092 |
| rs182145773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828209 | TCAGGGGATGAAGTA[C/T]CTGTTAAAAATTACG | 23092 |
| rs182151354 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810504 | ATCTCTTTCTTTTTT[G/T]TGTGTGTAGTCATTT | 23092 |
| rs182156076 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852886 | AGCTGCTGTCTCTGC[A/C]TGTCCTGTTGAAGCA | 23092 |
| rs182157398 | snp | C/G | 0.00688381 | 0.0582625 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090452 | TTCTACGATAGCTAT[C/G]TCAGTCGTGTCATTA | 23092 |
| rs182163022 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049200 | GTAATTCTCAATCTT[C/T]TAAACACACCAACAT | 23092 |
| rs182187470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011693 | GGTGCTGTGTGGCTC[A/G]ATTTGGAAACCATGA | 23092 |
| rs182201282 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989502 | TATTGTTATGCATGA[A/G]TTTGATCCTATCATG | 23092 |
| rs182216845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785435 | TAATGCACACTCACT[G/T]CCGAGGGGGCCTTTA | 23092 |
| rs182246914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214282 | AGCAGCAGGACTTCC[A/G]GAGACATTGTGAAGA | 23092 |
| rs182267110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177619 | GGCTGGCACTGCTGT[A/C]AGGAATAACAATAAT | 23092 |
| rs182270328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156432 | TCTGTGCACTGGTTC[G/T]CAGAGTGTGGTCCTG | 23092 |
| rs182273381 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196475 | ATTTTCATCACCTGA[C/T]CAGTACACCACCCTG | 23092 |
| rs182279450 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201974 | GTCCTGAATATCCTT[A/G/T]TTAATTTTCTATCTT | 23092 |
| rs182282409 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182650 | ACTCTAGCTAATTGG[C/T]CTAGGAGATAATTCA | 23092 |
| rs182282851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997826 | TGTAATGCTGATATC[A/G]TGTCTAAGTGAAAGA | 23092 |
| rs182288907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843733 | TGAATTATAAGTCAG[A/G]TTCTAACCAATCTCT | 23092 |
| rs182290519 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982994 | GTTGGTGGTTATTTC[A/G]TGCAGGTGACCTGAG | 23092 |
| rs182291115 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132187 | GACTGATTTAACCAG[C/T]TGGCTGGCATCATTG | 23092 |
| rs182296098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219069 | GCCACCTGGCATGTG[C/T]TCAACATGTTATCAT | 23092 |
| rs182298193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807161 | TAATAACAGTGAATG[C/G]ATTGAGCCAACATCA | 23092 |
| rs182305664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199514 | ATTCAATGAAATGGG[A/G]TTAGATTAGATAGGA | 23092 |
| rs182306679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832449 | GGAAGGCAAGCCAGG[A/C]GGAGAGCCTGCAGCA | 23092 |
| rs182311967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196122 | TACGTCTTAACAAAT[C/T]ATTATTTAGCAAACA | 23092 |
| rs182313045 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788569 | TGGGTTGGGAAAAGA[A/G]CATCATTACTGAACA | 23092 |
| rs182313197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872659 | TGACTTTTTAATGAT[A/T]AGGGCTCTTGAGAGT | 23092 |
| rs182316491 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856291 | GGCCAGGTGGCAGTC[A/G/T]GTTGGTTGTGTTGGT | 23092 |
| rs182325539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159170 | GGGACACAGCCAGAC[C/T]TTTCAGAAATGGAAT | 23092 |
| rs182331231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891863 | TGAAATATGCTTTCA[A/G]TGTAATTATCTGCTT | 23092 |
| rs182331500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156169 | CTGAGGGATCTTATT[C/T]GTAGATTCAGATTCT | 23092 |
| rs182332736 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872111 | ACTGGGGATTGGATT[A/T]GTATCCAGTGCCCCC | 23092 |
| rs182336206 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912092 | ACAGAGGCAGGAGAA[A/G]CAGAAACCCTAACAA | 23092 |
| rs182338122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929225 | TGATGTTAGTCACTG[C/T]GCCCGGCCTATCCTC | 23092 |
| rs182344647 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952361 | ACTGGGGAGGTTTCT[C/T]TTCTGGGAGTGTTGT | 23092 |
| rs182353841 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911304 | AAAGTCTTCTTCTTT[C/G]TACTTTCCCTCACTC | 23092 |
| rs182357895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171988 | TTAGACTGGTTTCAA[C/T]AGATTTATTAAGTGA | 23092 |
| rs182359829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209237 | CTCTGAGATTTGGGG[C/T]CCTGTTTCTTGTCAA | 23092 |
| rs182374420 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951442 | AAGAGGAAGCACCAA[C/T]ATTTATTGCTTATTT | 23092 |
| rs182375387 | snp | A/C | 0.125182 | 0.216612 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132876 | TAAAAAAAAAAAAAA[A/C]AACTGTTATCTTCTG | 23092 |
| rs182379364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106932 | GGGCTCAGCTCACAG[G/T]TCTCTTCCCTAGAGA | 23092 |
| rs182412107 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108537 | ACTTTGGTAGACTGG[A/C]CCTTGAAATAAAGCT | 23092 |
| rs182422057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070991 | CTTATATGGGACCAC[A/G]AAAGACCGTGAATAG | 23092 |
| rs182439073 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028006 | CCACAGCCCCCAGTT[C/G]CTTTCTGACTGTCTC | 23092 |
| rs182454087 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803208 | AGATAAAATATGGGA[C/T]ACCCAGTAAAATTTG | 23092 |
| rs182455502 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100086 | GATACATGAAAGGCA[A/G]TATGAGAAGGTCCAA | 23092 |
| rs182459457 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139005 | TTCTTTTAGGGTTAG[A/C]TGTTGTGACCTAGTC | 23092 |
| rs182460853 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992194 | TTCTGTATTAAGGCT[A/G]TGAGATACTTTATGC | 23092 |
| rs182461166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118985 | AAAACAGTGGGGCCC[A/C]CTACAGGTTTACAGT | 23092 |
| rs182462015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840628 | CCCATGGCAAGTGGT[A/T]GTTGTCATCGTCTTA | 23092 |
| rs182462790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074075 | ATGGTGGTAAAACTT[C/T]TTATCTTAAAAAGGT | 23092 |
| rs182462968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780792 | TCTGTGACCGGAGAC[C/T]GTGACTCTGGTCTAG | 23092 |
| rs182465930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868189 | TAGAGAAGTCAGGGA[A/G]GGCTTCCTGGAGGAA | 23092 |
| rs182473530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052486 | AAAAAAAAAGAAAAA[A/G]AAATTATGCTCTTTA | 23092 |
| rs182473681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030306 | CCTCATTTAGATGGC[C/T]GAGTTAGTGTAATAT | 23092 |
| rs182481540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804439 | TCACTGAATGGAAAC[G/T]TACTGAATTCTTCCA | 23092 |
| rs182498713 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948129 | ATGCGGCACTTTAGA[C/T]GTGGCACTTTCAAGC | 23092 |
| rs182559130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177011 | TGGCTCTGGCACTCA[C/T]CTGTCATTACTTTGA | 23092 |
| rs182566788 | snp | C/G | 2.71065e-05 | 0.00368138 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143214059 | ATGACTCAGAACTTT[C/G]GTTCACAGCAGGCAC | 23092 |
| rs182601890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138038 | GTGTGTCTTATTTGC[C/T]AGAAGGGGTTTTTCC | 23092 |
| rs182602870 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223549 | CATCTCTGCTCCCAC[C/T]CTTGCCTGCCTCTAA | 23092 |
| rs182607866 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190727 | GAAAAAATGAGAGGA[C/G]AAGCCACACACTGGG | 23092 |
| rs182611056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846832 | TATGTATTGATTAGT[A/G]TGCTTAAAGCATACA | 23092 |
| rs182617709 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125217 | TAGCTAAGGCATACA[A/G]TCTTTTCTCTCTTTG | 23092 |
| rs182620772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882857 | CATCCTCAATTTATA[A/G]TTGAGGAAATTGAGT | 23092 |
| rs182622922 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812103 | CTCCCCACCCCGTCT[A/G]CTGCCTTTTCCCCCC | 23092 |
| rs182623707 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186522 | CTCTCTTTGATAACA[C/T]CAGCTTTTCTTTGAG | 23092 |
| rs182625045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209322 | TCCTTCCTACTTCTT[A/C]CTACCTCCCAAAGTA | 23092 |
| rs182634053 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922864 | TAATATTTTATTTTG[A/C]CTTCCTGCTGGTTGG | 23092 |
| rs182634369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853332 | AGTAGCGGGGACTGC[A/G]GGCATGTGTCACCAC | 23092 |
| rs182642810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173246 | AGAAAATAAATATGG[A/T]GTGCCCTCGAACTCT | 23092 |
| rs182647649 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828386 | ACCACAAAATGAGTC[A/T]TTATGACTTAAGTTT | 23092 |
| rs182649584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152751 | TCTCTTGGAACCCAG[C/T]CACCATGTAAAGAAG | 23092 |
| rs182650217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869064 | TGGCGTCCAGGAAAG[A/G]AAGAGATTAACAAGG | 23092 |
| rs182657543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089703 | GATCTAGTTTATCCA[A/G]TCTACATTTTTATTA | 23092 |
| rs182662188 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192057 | CCTGTGGAGTCTTTC[A/T]TAAAAATACAGTCTT | 23092 |
| rs182663291 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888292 | TTTCTACGTCTCTAT[C/G]TGGGGAGGGATGTTG | 23092 |
| rs182666015 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782875 | TTAGAGTGTCCTTGT[A/G]AGATAGTGGTTCTTA | 23092 |
| rs182666570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150062 | AATGTAATGCTAAAT[C/T]AGGCATCAAAATTAG | 23092 |
| rs182671658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907634 | AATTATGGGTTGTGG[C/T]TTTTCCAGCTCATGA | 23092 |
| rs182674993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926271 | GTTTTCTCCATGGCT[C/T]CTGCAGTGTGAGAGG | 23092 |
| rs182681390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153089 | TAGAAAGGTATGGAA[C/G]AGTCTCACTATAGTA | 23092 |
| rs182682470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065456 | TCTACGTATATGAAG[G/T]TAATCCATGGGGCAT | 23092 |
| rs182684559 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116168 | TCAGAAAGTTTGAGC[A/G]CTACTATTATAGAGT | 23092 |
| rs182686164 | snp | A/G | 0.000546091 | 0.0165151 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143134087 | ACGCTCTTCCACACC[A/G]TTCAGTCAACAGAGA | 23092 |
| rs182688759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964241 | AGCATGAAATGTAAG[C/T]AGGCTTAATGCAGTT | 23092 |
| rs182689733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045403 | AGTTTGAATCTCTCA[A/G]TTACGGAATCACCAG | 23092 |
| rs182699855 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096327 | GGTGCAGATCCAGAT[A/T]TTCTAAAATTATGAC | 23092 |
| rs182703581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025020 | ATAAATGAGATTAGG[A/T]TGGACATCCTTTGCT | 23092 |
| rs182707701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008274 | ATAACTGATGTGCAT[G/T]TTAGCCAATAAACAG | 23092 |
| rs182711413 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888190 | TTACACATGAGGAAA[C/G]TGAGGCTCAGATAGG | 23092 |
| rs182713903 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821557 | CATGGCTGGGAATTA[C/T]CATTCCTGGACCAGC | 23092 |
| rs182718044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990396 | TCTTTGTGATGGGTT[C/T]GAGCATCCTCCTTTA | 23092 |
| rs182722762 | snp | C/G | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971930 | CTCACGCCTATAATC[C/G]CAGCATTTTGGGAGG | 23092 |
| rs182737773 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786490 | TGTTTTTAGAGATAG[A/G]ATCTTGCTGTGTTGC | 23092 |
| rs182754227 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824075 | GGGACCAGCTCCACA[A/G]TGGGTTTCACACCAT | 23092 |
| rs182761908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775031 | AATTATGAATAGAGC[A/C]GATATAAACATTTGC | 23092 |
| rs182762677 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805393 | AGGTGTGACCCACCA[C/T]GCCTGGCCCACATTT | 23092 |
| rs182763800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815738 | ACCACTTTCAGACTC[A/T]TTCGAGCCTCACTTT | 23092 |
| rs182767153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844582 | AATAAGAACTCTTTT[A/G]GGCTGGGCGTAGTGG | 23092 |
| rs182771402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775926 | TTTTTCTTTCCATTT[C/T]GTTTCCCTTCAGTAT | 23092 |
| rs182793220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929686 | CCAAGGCCAAGTGGC[C/T]CACCCTTCACAGCCT | 23092 |
| rs182799388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953008 | GTCACAGCACCCGGC[C/T]CCAACTGTGCTTTTT | 23092 |
| rs182830496 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226784 | CACCGAGTGCTTTTC[A/G]GTGAGAGGCAAAGAG | 23092 |
| rs182875516 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214553 | TTTTTCCTCACTTTT[A/G/T]TCTGGGCAGTGGGTG | 23092 |
| rs182881230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148744 | TGACCTTCTCAGGTT[C/T]TCCTATACCCACTTT | 23092 |
| rs182890682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820932 | TGACTAGCCTTCTGT[C/T]CCTCCACCTCCGCTA | 23092 |
| rs182895982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110532 | GTAACAACAGGAACC[A/G]GCATTTGCAGCACTT | 23092 |
| rs182899011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109461 | GTTTGTTTTTGTTTT[C/T]GTATTTTTTTTTTTA | 23092 |
| rs182900388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902736 | AGGTTACATAGTAGT[C/T]AGTGTTGTCTCAGAG | 23092 |
| rs182904936 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839425 | AGAGCGGTCATATAA[C/T]TTGCCCAAGGTCATC | 23092 |
| rs182907972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166753 | TCTGTAGCCACAGTG[A/T]ACTGGGTTACCAACC | 23092 |
| rs182910177 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128556 | AGCCTCTGAATTTGG[C/T]TTCTTAACAGTTACA | 23092 |
| rs182911195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860714 | CACCCCTGCTGTCAC[C/T]TAGCTTTCTTCTACC | 23092 |
| rs182911345 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082186 | GGCTCTTAGCATAGT[G/T]ATAATGCCGTGATTG | 23092 |
| rs182911505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792739 | CTGTGGAATGAGCAG[C/T]GTTGGAGGATTTGAA | 23092 |
| rs182912685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877627 | GGGCGAAGGACTTGG[A/G]GGTCCTGATTCCCAG | 23092 |
| rs182914913 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209700 | GCAGGAGGATTGCTT[C/G]AACCTGGGAGGCAAA | 23092 |
| rs182916527 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091526 | TTATTAGTTTCTAGA[C/G]CAAAGAAAGCCAAAC | 23092 |
| rs182917123 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897556 | CTGAAATTTAAGGGA[A/G]GGGCCCAGTAGCCTG | 23092 |
| rs182917511 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820181 | CAGGTGGTTCTCAGA[C/T]CTCACATTGAGGAAC | 23092 |
| rs182921841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040867 | GAGGTAGTCAGTGCT[C/T]GATAGTATAGGCCTT | 23092 |
| rs182922315 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229192 | AAGAGGTCAGATGCT[A/G]GGAAACTTGAGAATT | 23092 |
| rs182922693 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860284 | ACTGGTTGAATGCCC[A/G]TGAAGCCGCCCTGCC | 23092 |
| rs182924280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942823 | TCTCACTCTGTTGCC[C/T]ATGCTGGAGTGCAGT | 23092 |
| rs182926480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204619 | CCTGCATTCCAGCCG[C/T]ACCCCCAGATAATTT | 23092 |
| rs182927263 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021481 | TTATTGGCCTTGTAC[A/G]TCAGCCTTTGTACGT | 23092 |
| rs182929335 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051502 | AAGAGTGTAAATGAC[A/G]TCTCTGTGGCATATT | 23092 |
| rs182931082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072671 | ACTGCATATTCTCAC[G/T]CATGTGGAAACTAAA | 23092 |
| rs182938883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004260 | GGTTACAGTTAGTCC[A/G]CAAGGACTCAGATAT | 23092 |
| rs182944531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039854 | ACAAGTTCCTCTTCC[C/G]CCTCTAAAATGAAAA | 23092 |
| rs182945289 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986854 | GCTCTGTTCTGTTCA[A/C/G]TTGGTCTGTATCTCT | 23092 |
| rs182945862 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129598 | CTGCACTCCTTATCT[A/G]TGTGACCTTGGACAA | 23092 |
| rs182961874 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003370 | ATAATTTGCTCATCA[A/G]GGTCATCATGACCTG | 23092 |
| rs182963032 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896663 | CCTGGCATCCTGTTG[C/T]AGTGTGTCCATGTCT | 23092 |
| rs182982651 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971451 | TCACTGAAGCCCTGG[A/G]TTAGCTGCTATCTCC | 23092 |
| rs182984349 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967868 | GAGGTGGGTAAACTG[A/T]TAAAATCAGTGATGA | 23092 |
| rs183008628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018212 | CTTTTCTTTTTGATA[C/T]GTAAAAAGTTCCTAC | 23092 |
| rs183008687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088551 | CATGTGAAGCAGAAA[A/G]AACCCAAGATAATCT | 23092 |
| rs183034089 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983299 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGACCC | 23092 |
| rs183041230 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781917 | AGATGGGGTTTCACC[A/G]TGTTACTCAGGATGG | 23092 |
| rs183052692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795502 | GTGCCAATCTCAGTT[C/T]CATTTCTGGTGTGTT | 23092 |
| rs183054424 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802053 | GAAGCTCCAGAGGCC[C/G]TGAGAGTTGAGATGA | 23092 |
| rs183101481 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926601 | TAGGCCACTTTGTTG[C/T]GTTACTCAGGAGGAG | 23092 |
| rs183105159 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144814 | TGGTCTTATTCTCTA[A/C]TCTTTCCCTGGAATA | 23092 |
| rs183108702 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949032 | ATCGCTTGAACCTGG[C/G]GGGCGGAGGTTGCAG | 23092 |
| rs183115249 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873008 | CAGACTTGTGGGGGA[A/G]ACTGCACTGACTGTG | 23092 |
| rs183115570 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228108 | AGAGGTTAAGACATT[C/T]TATACTGTTCTACGT | 23092 |
| rs183118943 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160382 | TCTTTTTAACCTTAA[A/C]CTTTTTTGTGTTACC | 23092 |
| rs183123847 | snp | A/G | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968438 | TTGTTTTTGTATGAT[A/G]TATTTCAAAAAATTT | 23092 |
| rs183125865 | snp | A/C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912792 | GTGCTTTGTGAACAC[A/C/G]TTCTGGGGATATTTG | 23092 |
| rs183133088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200463 | AATGGTTACAGAAAT[C/T]AGAGTATACCATACA | 23092 |
| rs183166791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159879 | TGATCTGTGGCGGAA[A/G]GAACACTGCCTTTTC | 23092 |
| rs183187681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801040 | AATTCAGTCATCAGC[G/T]TACTGCAGGTGCCGT | 23092 |
| rs183199078 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838518 | TAGCCACGCTTATTG[G/T]CTGTGTCACCTCAGA | 23092 |
| rs183205651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882372 | GGTCATGTAGTCATT[C/T]AATGTTAGTGATTAT | 23092 |
| rs183209185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857011 | GAAGGCTCTAGGGAA[G/T]AATCATTCCTGGCCT | 23092 |
| rs183210144 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769451 | CGAACAGAGGGACTA[A/C]AGGGCAACGCACTGG | 23092 |
| rs183211412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833680 | TTTCTGTGTGAGCAA[A/G]GGTCATGTTTGGCTT | 23092 |
| rs183213599 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017268 | TCTCGAAGTTTCTCT[C/T]AGGGCATACGGTGCC | 23092 |
| rs183214689 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874535 | CTCAGGGCCATTGCA[C/G]GTAATGCTTATTGCT | 23092 |
| rs183215408 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055821 | CAATGAAACATAGTT[G/T]TGTCTATTCATTTAA | 23092 |
| rs183217326 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997026 | ACAACAGACTGTTGA[A/G]ACTACTGAACTCTAT | 23092 |
| rs183218528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901469 | AGACTCAGGACACCC[C/G]ACTTCCTTTTCTGCC | 23092 |
| rs183225533 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922621 | TCTGTTTAAACATTA[C/T]CCTTTACCTGGCTCT | 23092 |
| rs183225725 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060738 | CTGGGCTCTGTGGGT[C/T]TACTCAGTCAGGCTC | 23092 |
| rs183227645 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877276 | CTCAGCAAGCAAAGC[C/T]GCACCTTCTCTGGGA | 23092 |
| rs183228341 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981012 | TCCTGGGTGAGTAAT[G/T]ATGTTTGGATATCTT | 23092 |
| rs183230438 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942054 | CCAGCACAGTGGCTG[G/T]CAGAGTAAGCATTCA | 23092 |
| rs183232221 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020809 | ACGCCCGGCTAATTT[G/T]TTTGTAGTTTTTAGT | 23092 |
| rs183242297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916221 | AAGTGTGAAGTATGT[A/G]ACTTAGAATATGGGA | 23092 |
| rs183244768 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179026 | AGGCACCTGCCACCA[C/T]ACCTGGCTAATTTTT | 23092 |
| rs183253546 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986349 | GCCCACTTTTTGATG[A/G]GGTTGTTTGATTTTT | 23092 |
| rs183260098 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139207 | CATCTAATAATAACA[A/G]TAAAAATAAAAATAA | 23092 |
| rs183260249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100688 | GACTCTGCTGGCTTT[A/G]TGGGCAGGAAATGAA | 23092 |
| rs183271361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993465 | TGAGCCACCACGCCC[A/G]GCCCAATTTTTGTGT | 23092 |
| rs183277664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977265 | TGGGTAAAGAAAATT[A/G]TATAAAAGTAACACC | 23092 |
| rs183278518 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035663 | CATGTAGGCCAGGTG[C/T]GGTGGCTCACGCCTG | 23092 |
| rs183279224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020115 | CCGGATGAAACTGCA[C/G]GAGTCCAGGCTTCCT | 23092 |
| rs183280712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002366 | GCTGTATAACTATTT[A/C]CAAAAACACTGGGTT | 23092 |
| rs183291916 | snp | C/T | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965716 | TCTTATATTTTATTA[C/T]ACTGGAACAGCTCGT | 23092 |
| rs183291972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998824 | TATGGCCTGTGCAAC[A/T]CGAGACGGTGAGCTA | 23092 |
| rs183293955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062061 | TTTGACAGAATAAAG[A/G]CAGCCCACGGTGTCT | 23092 |
| rs183297460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124414 | AATTATTTTATTACT[C/G]TCAATTCTGTGAGTC | 23092 |
| rs183300652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089005 | ATGAGTCAGGGTGGA[A/G]CAGGTAATTGAAAAA | 23092 |
| rs183306321 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965056 | CCCTTCCCTGCCTGG[C/T]AGCCAAGGCAGAGAG | 23092 |
| rs183306784 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106432 | AATTCCCATGGAAAA[A/G]GAAGTGAACTCCTTT | 23092 |
| rs183306856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796331 | GCCTCTGTCTTTGAG[C/T]AAATTATTTAATCTC | 23092 |
| rs183314513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833460 | AGATAATTTTCTTAC[C/T]TCTTAACTTTAAACA | 23092 |
| rs183315827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067582 | AGTTTTTCTTCCAGC[A/G]GTTTAGCATCCTGAT | 23092 |
| rs183322961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045909 | GAGGTCAAGGTGAGC[A/G]ATCACCTGAAGTCAG | 23092 |
| rs183327826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028467 | CCCTATGGGGTTATC[A/T]TAAAGATAACATGAA | 23092 |
| rs183375203 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892379 | ACAGAAATCCCAGCT[C/T]TGCCGTATACTAGCT | 23092 |
| rs183389720 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878306 | CCATAGAATCTTAGC[A/G]ATGGACAATTCAGCC | 23092 |
| rs183391883 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898012 | TCTATGCAAATCGAC[C/T]GTGTTCATTTGTTTC | 23092 |
| rs183402477 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917980 | CAGTTTGTTAATCCT[C/T]AAATCCCTGACACAT | 23092 |
| rs183409953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937281 | ACCAAAGAGAATATG[A/G]CGAATAAGCACAGGA | 23092 |
| rs183416215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956929 | GGAAATACCGGCCCT[C/T]GTGATTCAATTATCT | 23092 |
| rs183436531 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181915 | TGGTCTACATGGTCA[A/G]CCATTGTTTACCTGA | 23092 |
| rs183444040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080082 | TGAGTCCTGGTCACT[C/T]TTTTGCCTATAAGAT | 23092 |
| rs183454156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144011 | AGGCGGGCAAGCATT[C/T]TCACTGACTTCAACC | 23092 |
| rs183461841 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105189 | GAGACCAGCTTGACC[A/G]ACATGGAGAAACCCT | 23092 |
| rs183468934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157034 | GACAGAAAAATAGCT[C/T]TCAGGCTATGTGATA | 23092 |
| rs183480038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197282 | CTTCACCTTTGCTAG[A/T]TAATGCTACACTATT | 23092 |
| rs183486546 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119808 | AAAAGTACACATCTG[C/T]TAATAAAATTGGTTG | 23092 |
| rs183501386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217782 | GGCGCTTCCACTGGC[C/T]GCCTGACACATCTTG | 23092 |
| rs183514183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157730 | ATCCTTTCAGAGAAC[A/G]GAGATTTTGTTTATA | 23092 |
| rs183514880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956427 | CTAAAAATTTTAAAA[A/G]TTAGCCAAGTGTGGT | 23092 |
| rs183520429 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186030 | GTTAAGAGGCCATGG[C/T]TCAGAAGGAAAAGGA | 23092 |
| rs183525412 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991178 | TGGATGCCCCTCCCC[C/G]AGCCTTGCTGCCGCC | 23092 |
| rs183526264 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203906 | GGGAACATCACACAC[C/T]GGGGCCTGTCAGGGG | 23092 |
| rs183527925 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222554 | ATGCAGCGTGACTGA[C/T]TCTGTTGCTACCTGT | 23092 |
| rs183529670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794260 | TCCTTGAGATAATCC[C/G]TGAAGCCGACCTGAC | 23092 |
| rs183531048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149378 | AGCAGTACCAGCATC[A/C]GCCCTGATACCAGCG | 23092 |
| rs183531351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973043 | TAATTGTTAATAAGG[A/G]TTGATTTGGGGTTGT | 23092 |
| rs183531970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182201 | CTTACTACTCTTACT[A/G]CTGTTAACTCATCTC | 23092 |
| rs183534157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772346 | TCCTTTGTCAATAAT[C/T]AAGGCCATTCTTGGT | 23092 |
| rs183538341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083128 | GACTTTTTCTTCGTC[G/T]TCTTCCTTTTTCTTT | 23092 |
| rs183544984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165909 | GTATCTACCTCCTAG[C/G]GTTGTTAGGATGAAA | 23092 |
| rs183553524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816339 | GATATCATTTTGATG[C/T]AAAGAGTGTTAGGTA | 23092 |
| rs183557702 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856683 | TTTCTTTTTTCTACT[C/T]TCAAGCAATACAGTA | 23092 |
| rs183558299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992772 | CAAAGATCAGCTGCC[A/G]TACAGAGACCATATG | 23092 |
| rs183574293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202963 | TGTAAGACCTAAAGC[C/T]GTAAAAACTCTAGAA | 23092 |
| rs183575446 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221555 | GTCTTGCTCTGTCGC[C/T]CAGGCTGGAGTGCAG | 23092 |
| rs183599444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117088 | AGGGATCTGAAAAGC[A/G]TGTGTCAAAGACTCC | 23092 |
| rs183601664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184313 | CTCCCCCTAACCTGA[A/G]TTAATGTATTATTGC | 23092 |
| rs183610794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136000 | GGCTATGGGGTAATG[C/T]GCTTCTCAGGTTTCC | 23092 |
| rs183618325 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097547 | ATGCAATGGCCGGGC[A/G]CGGTGGCTCACGCCT | 23092 |
| rs183625024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056780 | ACTTGTGTCTCTCCC[A/G]GGTTCCTTTCAGCCT | 23092 |
| rs183631620 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081157 | AGCTCTCAGCATACA[A/G]ATTATTCTTTCTTGT | 23092 |
| rs183637315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036640 | TGGTATGGGCTCTAG[A/G]GCAAGTCTCCATGTA | 23092 |
| rs183645409 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930552 | CACCATCATCAACAC[A/G]CCCACTCATCTAGCT | 23092 |
| rs183657930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018637 | TGCCAGTGTTCTTGC[A/G]TTTTAGGTTTGCATA | 23092 |
| rs183659673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826447 | ATAAGTTTAAAGAGG[A/G]GTAAATAAGTTGCCC | 23092 |
| rs183664623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874892 | TTTCCTTGAAGAAAT[A/C]ATTCCCTAGCTAGAG | 23092 |
| rs183667838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857993 | GAAATTCAAAAGCCA[A/G]ATCAAGAAACACGTC | 23092 |
| rs183670833 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851385 | TACAGGCGTGAGCCG[C/T]TGCGCCCAGCCGGAA | 23092 |
| rs183679480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894085 | ATATTTTTGCATAGT[C/G]AAATAGTTACTATAG | 23092 |
| rs183696121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932518 | GCTGGCCTCAGCTGG[A/G]TGATGTAATCTTGTA | 23092 |
| rs183733659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936913 | TGTAAAATGTAACAC[C/T]TGAAAACTTTTAGAA | 23092 |
| rs183735662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201517 | AGGGGCAGGAGGGAG[C/G]AAGATTTTTATTTTG | 23092 |
| rs183769566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012297 | GACCTTCTTGGGCGA[C/T]TCCTTCAGTTTATGG | 23092 |
| rs183783347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787220 | AATGGGACCTGATGA[C/T]AGTGTCAAGTGTCTC | 23092 |
| rs183785531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977079 | CCCTGGGGTTAGCTC[C/T]GCCCAACCACACAGA | 23092 |
| rs183805943 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871125 | CGTCTATCGGGGGAT[C/T]GGCCTGTCCTTCAGC | 23092 |
| rs183806967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079031 | TGGCTGTGGGAAAAG[C/T]GCTAGGATTATTACT | 23092 |
| rs183809697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854945 | AAGGACCCCCCAGTC[C/T]CTTTTGTTCTCCTTC | 23092 |
| rs183811039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824183 | TCGCGTTCCCATGCT[C/G]TGTGTCTTAACAGCT | 23092 |
| rs183812863 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890903 | GAGCTTGCACTTGGG[A/C]AGCTCTCTGATGTGG | 23092 |
| rs183817262 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863845 | GCTGCAGAGGAAAAG[C/G]CATTCCAGAAACAAA | 23092 |
| rs183821151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198421 | GCCTGAAATGCGGTA[C/T]TGGAAAAGATTGAGA | 23092 |
| rs183825132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008871 | ATGACTCTGTGTATT[C/T]TCTGTTAATTCTGTA | 23092 |
| rs183828157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910020 | GTAGTGAAGAGGTTT[A/G]TGTGAATTAGTATAT | 23092 |
| rs183831644 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215616 | CCTTTTAGCAGTCAT[A/G]CCCCACTTACCACAA | 23092 |
| rs183834382 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034174 | CTGGTGCAGCTGCTT[A/G]GAAAACAGTTTGGCA | 23092 |
| rs183840459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113361 | CTGAAATGTAGCCAT[A/G]TGTTTCCCCAGAAGC | 23092 |
| rs183841348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142972138 | AGTGAGCCGAAATTG[C/T]GCCACTGCACTCCAT | 23092 |
| rs183841924 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950301 | ATCATGGGGTTTCCA[A/T]GTTGGATTAAAACTG | 23092 |
| rs183845734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141705 | TCAACTGTAAGTTAA[C/T]GGGAAACCAACTTTT | 23092 |
| rs183846791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791453 | TTTCTAAATATCTTT[C/T]ATAAGTAGCACTATG | 23092 |
| rs183855400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131207 | AATATTGTCTTGGAA[A/G]CAATTTTTCACGCAT | 23092 |
| rs183856761 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179768 | CATTTGTTATTGTGG[A/G]GAAAGTCCTGTGCTG | 23092 |
| rs183858637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158001 | TACTTTCAAGGTTAT[A/C]AGATAATGCCTTCCT | 23092 |
| rs183859127 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893227 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 23092 |
| rs183871302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953319 | ACAAGCAAACAGATT[C/G]GTCACCTGCACTTAT | 23092 |
| rs183873494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121531 | TCTTACTTGATTGTT[C/T]TCTTATGAATTTATG | 23092 |
| rs183875964 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051923 | CAGTAACATTTGTCT[C/T]ACATCCAGGAACCAT | 23092 |
| rs183908349 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013094 | AAGCATCATATTTAC[A/G]AACAAATATCTATAA | 23092 |
| rs183939755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969645 | TGAAATATTAGAAAT[A/G]CTTATTGTACCCTTT | 23092 |
| rs183940668 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013348 | ATAAAATGTTAATGT[C/T]TGACCCGTTGCAGGA | 23092 |
| rs183942765 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993936 | TCACTTCCCAAAGTG[A/C]TGGGATTATAGGCAA | 23092 |
| rs183943121 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985981 | TACGTGTGTATGTGT[C/T]TTTATAGCAGCATGA | 23092 |
| rs183951502 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977931 | GAAACTGGAGCAGCA[C/T]CTTGAGAGGTTTCAT | 23092 |
| rs183987066 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806721 | AGTTATGTACCCCCC[A/C/T]ACTACTTAGACATCT | 23092 |
| rs183997025 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973571 | ACTCCATGCACAAGT[A/G]TTAGTTTTATTTTTA | 23092 |
| rs183999985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845107 | ATCCTGAGGAGCTGC[A/C]GCTCTTGAGGGAGGC | 23092 |
| rs184002777 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197988 | ATCCAGTTCCCCACT[C/G]TCAACCCCCTGAGGC | 23092 |
| rs184003682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025490 | ATGATGATCTCTTTC[C/G]GTTGAGAAATCAGTG | 23092 |
| rs184007802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907106 | GTCCTTAGAGGTTAC[A/T]TGTGGGCATTGACAG | 23092 |
| rs184014652 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055566 | GGGGTTCTAGCATTC[C/T]GGAGCAATACTCCAT | 23092 |
| rs184017703 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990627 | TGATGATGGTGACGT[A/T]CAGATGGGGTTTTGG | 23092 |
| rs184025690 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946833 | GTGTTCCCCAAAATC[A/C]TGCCCCATGACCTTT | 23092 |
| rs184048280 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913421 | TCCTTTCCTTCTCCC[C/G]CTGCCTCCTTCCTTT | 23092 |
| rs184050203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194933 | TCAGGTTTGTGAATG[A/G]TCACGCTGAAGGAGC | 23092 |
| rs184061311 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211350 | CCAAATCTAACTAGG[C/T]GTCCTGTATTTTATC | 23092 |
| rs184065438 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029339 | TGCTCACAGCAACTC[A/G]ACAATTTCCTGTATC | 23092 |
| rs184069687 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128971 | ATTACAGGGAGACTC[C/T]TAATCCTTTTAAATT | 23092 |
| rs184097229 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092027 | CAATAGTTTTACATT[C/T]AGGAGGCCTAATTAC | 23092 |
| rs184112902 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967004 | TGTGTATATAGTGCA[C/T]ATTGTACATATGTAT | 23092 |
| rs184116112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803746 | GGGATGTGTTCTTGG[A/G]CTTTAATAGCAGGTA | 23092 |
| rs184125332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089919 | GGGTGAAAGGGATAG[C/T]CAATTGGACTAAAGC | 23092 |
| rs184133678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143069906 | TTACACAGCTTGGTT[C/T]CCCAGAAGCCTGATT | 23092 |
| rs184139202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783249 | AAAAGTTCTAGCAGC[C/T]TGAGAACATGTCAGC | 23092 |
| rs184143219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954068 | AGCAAAGGCGTTTTT[A/C]AGCGAGAGCTGTACA | 23092 |
| rs184145248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822044 | ATCCCCCATAAAGCT[C/G]TTCTTCTAAGAGTTC | 23092 |
| rs184149956 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048032 | TTGTATCTTTTTAGT[A/G]GAGTCAAGGTTTCAC | 23092 |
| rs184155760 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026965 | TGACAGGATTGGTTA[A/T]TGGATTGGATGTGGT | 23092 |
| rs184158164 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214746 | TACAGGTAGACAAAA[C/G]GGGGAACAAGGCACA | 23092 |
| rs184162562 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861282 | CTAATTAAAGAGGGG[A/G]TAAAAGAAAGTGAAA | 23092 |
| rs184164949 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143068828 | ACCTCAGGCTTTTTA[A/T]GCACACTAGTCCACT | 23092 |
| rs184166559 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000514 | CTGAGTGCAATCCCA[C/T]TACTGGGTATATACC | 23092 |
| rs184167271 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010586 | ATTTCAAAACTCATT[C/T]TCTTTGGCTCATTAA | 23092 |
| rs184168143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025793 | CTGTCACCCTGGATG[C/T]CTGTCTTTTGCCAAG | 23092 |
| rs184181116 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064249 | GCCTACTTCATTCAG[G/T]TCTCCTACCTGCCTG | 23092 |
| rs184181117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111064 | TTACAGCAAAAGTAT[C/T]ATTCTTCTTGGGTTC | 23092 |
| rs184182843 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150527 | GGATGAAGAGCATTC[C/T]AGGTAAGAAGGATGA | 23092 |
| rs184183290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965994 | TTTGTTTTCTCTCTC[C/T]CACTCCTTTTCCCCT | 23092 |
| rs184186662 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179159 | CAGGCGTGAGCCACC[A/G]CGCCCAGCCATTTAT | 23092 |
| rs184189336 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130077 | AGTGATGGTGAGGTC[C/T]GTGTAGCTGTAGGTG | 23092 |
| rs184194921 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093293 | CATTTGGGCCATCTG[C/T]GGGTTACTAGGTTAA | 23092 |
| rs184198009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043118 | CAACCAAAATATTGG[C/T]ATTAATTTAGTCAAG | 23092 |
| rs184203276 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023201 | TTTAGGCCGTCATTC[A/T]GAGCAAACTCCCTGA | 23092 |
| rs184206286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006158 | CTTAGGAAGGCCTGA[A/G]TTGTCTGTTTCCACT | 23092 |
| rs184206478 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074391 | TCTGGTATCCTGGCC[G/T]TTTTCCATTAATCTC | 23092 |
| rs184220722 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924524 | TGAATGATAATACAA[A/G]TAAAGTCCTTAGCAC | 23092 |
| rs184231997 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110183 | ACTCCCCATCCCTTT[C/G]ATGCTGGCTGTTTCA | 23092 |
| rs184241354 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073543 | TTATTTCCCTATTGG[C/T]GGTAGGGGAGAGCAT | 23092 |
| rs184268219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847652 | GTGAGCCACCGTGCC[C/T]GGCCAGGATGATGAT | 23092 |
| rs184271233 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798783 | GCTTCTCCTTTTTCT[A/C]CTGGTCTTGTCATTT | 23092 |
| rs184272848 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136432 | CCGGAGCATACAGAT[A/C]TGCTCAGATATTTGT | 23092 |
| rs184274407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825217 | GTGCTTACAACAGTA[C/G]CTAGCACACAGTACA | 23092 |
| rs184280150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175100 | CCCCACATAAAAGGA[C/G]CCCAAATGTTCTCTC | 23092 |
| rs184283258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154846 | AGACAAGTGATAATT[A/C]ATAGCATTTTTTTTT | 23092 |
| rs184284529 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864552 | TCAGGTGTGTTTTTA[A/G]TAGTTCACAAGAATG | 23092 |
| rs184287917 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884449 | TACGGCTAATAATTT[C/G]TTAAAGAGAAGAGAA | 23092 |
| rs184290532 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902949 | TAGAGCTGTGATGCA[A/G]ATGCAGCAGAGGTCT | 23092 |
| rs184292286 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117330 | ATCTGTAAATTCATC[A/G]AGCTATAATGGATGG | 23092 |
| rs184298167 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047501 | GACTTATTTTAAGAT[A/G]TTGAATTGCTGGGTC | 23092 |
| rs184301276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210608 | TCCCCCAAAAAAGCC[A/G]ATAGCCCCAAACCCG | 23092 |
| rs184302892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923686 | TTCCCGATGTTTTAC[A/G]ACTTCAGTCTCTCAT | 23092 |
| rs184317436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166958 | TGATGAGGCAAAGTC[C/T]AGAAGAACTTTTTCT | 23092 |
| rs184321537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984524 | TAACATTTTGTATAT[A/G]AGAAACAGATCTGTG | 23092 |
| rs184327767 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187275 | TTAATTCAGTATTCT[C/T]AAGAATATTGTTTTC | 23092 |
| rs184330316 | snp | C/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009557 | TGGCATGATGTCTGG[C/G]ACATGGCAGGGGTTT | 23092 |
| rs184346663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174277 | GCCACTAAGAAAGAA[C/T]GAGGAGGCAACTTTT | 23092 |
| rs184353615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777791 | CGGCCAGTTGTGACT[G/T]TAGCAGAGTGAAGGC | 23092 |
| rs184363078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184231 | GCCAGCTGTCCCTTC[C/T]TGCCCATTAGGGGGT | 23092 |
| rs184363949 | snp | C/T | 0.031825 | 0.122064 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225248 | GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTCAC | 23092 |
| rs184369517 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163640 | ATTTTCAGTAGAGAC[A/G]GGGTTTCACCATGTT | 23092 |
| rs184376436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945508 | TTGAAGGTTTCTATC[A/G]CCAGCTGGTTGCTCA | 23092 |
| rs184378070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817224 | ATGGGAGGGGAGGGG[A/G]AAGGTGGAGGTGCTG | 23092 |
| rs184380106 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151579 | GCACGCAGACAATGC[C/T]ATATTATTCAATGAT | 23092 |
| rs184388922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188474 | TGTAATAGTCCTTCC[C/T]GGAGGGGAGTCTCCC | 23092 |
| rs184392203 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107929 | TGAAGTAAGAACTTT[A/G]TTGGCTTCATTCCCT | 23092 |
| rs184392387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193028 | CTGAAAATATTAAAT[A/G]AAAAATTATAAAAAC | 23092 |
| rs184394874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146213 | TTTGCTACAGTAATG[G/T]TGGATGCTGGTACCA | 23092 |
| rs184398737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125963 | CAAGCTATTAAAATC[C/T]ACTCTAGTTAATCTC | 23092 |
| rs184404320 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090287 | CCACCCTAGTGGAAA[A/G]GGGACAGTCTGGGCC | 23092 |
| rs184420971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070843 | CTTAAACTGGGGACG[C/T]GGAGGTTGCAGTGAG | 23092 |
| rs184424611 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778998 | GAAAGAGAGATGACA[A/G]TTAATTGGATGTGTC | 23092 |
| rs184430494 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194202 | TCTACATTCGTTAAG[C/T]AATGAGAAATTTATG | 23092 |
| rs184434469 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807990 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 23092 |
| rs184438490 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084502 | TTTATGGCCTGAGTT[C/T]CCACAGATTTGGAGG | 23092 |
| rs184453589 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154096 | ATTCCACAAATGTCA[A/G]TTGAACTCCTACTGT | 23092 |
| rs184478142 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant, missense, synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207391 | CATGCAGTGTTCAGC[C/T]TCCTCGTCAACTTTG | 23092 |
| rs184510727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798332 | TGGTACATGCAGTGC[C/T]CTCTGATGCAGCATT | 23092 |
| rs184524337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168000 | ATGGTCTAGGTGCTA[C/T]AGGATAAAGTGCTGC | 23092 |
| rs184552266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898957 | AAGTCTGAAGTCAAG[C/G]TTTTGGCACCAAGAT | 23092 |
| rs184564535 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865620 | ATGCCCCTTGGCTGT[A/C/G]GTTGCACATTCTCAT | 23092 |
| rs184567887 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937644 | AACTGGAAGTACTAC[A/G]GATGTCCTTTAATGG | 23092 |
| rs184570221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822534 | GGTACTGGAGATACA[C/T]ACACAAATACACACA | 23092 |
| rs184575006 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784613 | CTCATATCTCTTAAT[C/G]TGCCGTCTCAATCAG | 23092 |
| rs184575996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905805 | ATGGCTAAAATCGCA[A/G]TTGAACTCTTGCACC | 23092 |
| rs184579512 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804210 | AAAAACGACAGTTTT[A/G]TATGGTTCAACTTCA | 23092 |
| rs184584982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843629 | ACCACTACACTTCCT[G/T]ATGGCGTGTTTTTTT | 23092 |
| rs184594268 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224507 | AAATAAGTGGGGTCA[A/G]GCATTCGAGTTTTTG | 23092 |
| rs184596439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206963 | CTATCACCTGAAAAG[C/T]AGTTGTTCTGCAGGG | 23092 |
| rs184602803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879547 | ATGTCTTCAGAAAAT[C/T]GAAGCCCACCTTCTT | 23092 |
| rs184603232 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862779 | ACCTCTTCCAAGAAG[G/T]TCTGGCTTTCACTGT | 23092 |
| rs184618011 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899475 | GGAGGCACAGGGAGG[C/G/T]GGGAAAGATCTTTCC | 23092 |
| rs184624402 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, missense | ARHGAP26 | GRCh38.p7 | 5:142919278 | ATGAAGGCAGAAGTC[A/G]AGGTGATGCACCTAC | 23092 |
| rs184634792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777016 | TTATCCTGGTGACCA[A/G]TGAGGATGAGCACCT | 23092 |
| rs184649206 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796829 | CTTCTGCCTGGTGTC[G/T]CTGGTACCATCCCTG | 23092 |
| rs184654435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042904 | AACTATGATTATTTG[C/T]GAGGTACTCTAGCAA | 23092 |
| rs184666313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816824 | GTCCTTGAGCAGAGG[G/T]TTAGTGTGATCAGCA | 23092 |
| rs184674882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005991 | AACTCCCCAGTGGTA[C/T]CATAGGCTTCAAAAC | 23092 |
| rs184692817 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918929 | TGAAATTCAGTTTAA[A/G]GACTCTAGCATTAAT | 23092 |
| rs184711078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794437 | AAGTAAATTGAGCAC[A/G]GTCATCTGTGGAAGA | 23092 |
| rs184712040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957621 | TCTCTTACGTAGTTT[A/G]ATCTAGATTTCCATG | 23092 |
| rs184735939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861843 | GATGGGATTTTGAAC[A/G]CTGGGAGTCTGTTAA | 23092 |
| rs184738151 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905271 | TGTTTTTTTGCACTC[C/T]CATGTCACACACTTT | 23092 |
| rs184740529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923942 | TCTCCGCTCACTGCA[A/G]GCTCCGCCCCCCGGG | 23092 |
| rs184756441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830710 | TTCTTGTGGGAGAGA[C/G]AGACAGACAGATACA | 23092 |
| rs184797659 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813000 | TGGAGTGCAGTGGCG[C/G]GATCTCGGCTCACTG | 23092 |
| rs184801825 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854107 | AAAAGCTTGTCACAC[A/C]AAAAACTGCATGTGT | 23092 |
| rs184801976 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188215 | CTACTAAGTACAATA[C/T]GTGGGGGCATTCACA | 23092 |
| rs184802284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063751 | CCAAAGGCTACCTCA[C/T]TCTTCTAGCTTCAGC | 23092 |
| rs184808476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829465 | AATTAGCAAGAAAGA[A/G]CAGTTCTGTGAATAG | 23092 |
| rs184813578 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022623 | CTTAACACAAGGCTA[A/C]GTTTTTAAAATTAGT | 23092 |
| rs184819611 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870705 | TCCCTGCCTAACCCA[C/T]GGGCTGACAGCCTCC | 23092 |
| rs184843957 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773153 | TCCGATATCATGAGA[C/T]GCTTGCTGCGTGGTA | 23092 |
| rs184848337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018303 | ATCTGTCTGTTAATA[C/T]GTGGTATCCTTCTTT | 23092 |
| rs184860075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999463 | GAGAAAGAGGAGAGT[C/G]AGGCGGGTTAAGGCT | 23092 |
| rs184864993 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983952 | AATTGAAAATCCAAC[A/G]AACAATGGCTTAAAG | 23092 |
| rs184865618 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813700 | AATCTTCTTTTCTTA[A/T]AAGGTCACCATATTG | 23092 |
| rs184867728 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842940 | CTCCTTGAAGAATCA[A/C/T]ATCAGTTAGATCGAC | 23092 |
| rs184873044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965387 | GGGTATTGTTCCTTG[A/G]CACTTTTTGATACCG | 23092 |
| rs184882387 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039354 | CTGGCATTACAGGCG[C/T]CTGCCACCATGCCCA | 23092 |
| rs184883657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878906 | TCCTGTCTTGGTAGA[A/G]CAACACAAAATCAAG | 23092 |
| rs184892984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835227 | TTGAAGTTAATGCTT[C/T]AACAACATGAAAACA | 23092 |
| rs184899198 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202466 | GGATAGGAAGAATCA[C/G]TATCATGAAAATAGC | 23092 |
| rs184913881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163209 | GGGAGATCAGATCTA[C/T]GTATGTGGGGGAGCA | 23092 |
| rs184915546 | snp | C/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875636 | CCCAGTAAACAGGTA[C/G/T]TTTGTAATGAAGGTA | 23092 |
| rs184917129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980168 | CCATCTACTCTTTGT[A/G]TGTGGCTCCTTTTAT | 23092 |
| rs184917988 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125738 | GAAATAATAATGATG[A/T]TAGTAATAGCTAACT | 23092 |
| rs184919187 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022355 | TGGGATTACAGGCAT[G/T]AGCCACTGCGCCTGG | 23092 |
| rs184923695 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097754 | ATGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 23092 |
| rs184928270 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943898 | GCTTAACCTTTGGGG[A/T]ATAGGATTAGTTGTG | 23092 |
| rs184932584 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915184 | TTCCCTCCTTTATGA[C/G]TCCCACAACAGCTGT | 23092 |
| rs184938594 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143058236 | TTCCTTAGTTTCCCC[A/C]TCTGTCTAATATGGA | 23092 |
| rs184982230 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103150 | CCTTGCCTGGTATGT[C/T]GTCTTCTTTACCTGT | 23092 |
| rs184986583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183388 | GATAATGAGAGCCGT[A/G]TGCTCCGTGACCTGC | 23092 |
| rs185003662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220109 | CTGAAGGAGATGGAC[C/T]CAGTGCATCCAGTAG | 23092 |
| rs185003803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818893 | CCTTCCCTGACCCTA[C/T]GATAAGGTTCAAGCC | 23092 |
| rs185011936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859204 | ATCAGGAGGGAAGCG[A/G]GGAGGCCAATTAGGA | 23092 |
| rs185021546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081582 | AATTACCTACCATCC[A/G]AAGACGGTGAAAACA | 23092 |
| rs185025470 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030701 | CATTTTGACACACTG[C/T]CCCTCGGCAACTCTC | 23092 |
| rs185031110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145727 | GGCATCAATTCAATC[C/T]ACTTTTTCCAAATCT | 23092 |
| rs185036778 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163804 | CTCCAGGAGGCTTCC[C/T]ACCTCTCAGACCCTA | 23092 |
| rs185039220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894636 | AGAGTGGAAATGGGA[A/G]TCCAGAGGGGAGGGG | 23092 |
| rs185044160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107515 | TCACCCACCTTTTCT[A/G]TTGAGCCAGGCAAAG | 23092 |
| rs185044864 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156170 | TGAGGGATCTTATTC[A/G]TAGATTCAGATTCTA | 23092 |
| rs185047388 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994537 | AAGGCAGAGAGTAAC[C/T]ATTGTGAAGGCATTC | 23092 |
| rs185049011 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118636 | AACTAGCCAGGTGTG[A/G]TGGCGCATGCCTGTA | 23092 |
| rs185050245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933816 | AGGAGAAAGGATACT[A/G]TGAATAGTTGGCAGT | 23092 |
| rs185053954 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138278 | TATAAGACAGCAAGT[C/G/T]GCTCCTCATATCATA | 23092 |
| rs185057789 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082000 | GGGTAACAGAGGGAG[A/T]CTCCATCTCAAAAAA | 23092 |
| rs185065382 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099594 | TTCAAATTCATTTTC[G/T]CAGTGTCACTCAGTG | 23092 |
| rs185068815 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120876 | ATGACCCAAGTTCTG[G/T]CTCCTACAGATGAGG | 23092 |
| rs185069322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060313 | TTCTGGTTCAAAGGC[A/G]AGCATTTTGTATTGT | 23092 |
| rs185079306 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900487 | TTGTCATAATCTGGG[G/T]TTTATCTTCACAGGG | 23092 |
| rs185079329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083846 | TCTTTCTCCCATCTT[A/G]TATCTCAGACTTATC | 23092 |
| rs185080650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142959429 | TGTTGGTTAGCTGTG[C/T]TTTCACCTGGACTTG | 23092 |
| rs185081363 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920755 | ATAAACTTATCTTCA[A/T]GGAGCTTACCTTTGA | 23092 |
| rs185085482 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101678 | AACAGACACACACAC[C/T]GTTGCCTTGAACAAT | 23092 |
| rs185087932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062839 | CAAATCTAGAAGATA[A/G]GATTTAACTTACCAA | 23092 |
| rs185088372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159639 | CTGATCTGATGTAGG[G/T]TCTGAGTGGTGGTAT | 23092 |
| rs185092932 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940189 | TGCGGCTGACACTTG[C/G/T]GTTTTCCTTTCTTTG | 23092 |
| rs185094039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200173 | TCTAATTTTTTTCTA[A/G]TGATCATGCTCAATG | 23092 |
| rs185095333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015128 | GAGGCCTTTATGAGA[A/T]GAAAAAAAAATGTTC | 23092 |
| rs185097975 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181603 | GTATCTCCTCAGTGC[A/C]AAGCACAGTGGCTGG | 23092 |
| rs185103047 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084824 | GGCCGAGGTGGAAAG[A/G]TCACGTGGTCAGGAG | 23092 |
| rs185103719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960697 | AAGGCTAAGCTTAAT[G/T]TATTGAGAAAAGTAG | 23092 |
| rs185103908 | snp | A/G/T | 0.000922084 | 0.0214544 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041779 | GACTTGTGTTCTGAC[A/G/T]TGCCTCTAATTAAAT | 23092 |
| rs185105761 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995356 | AGTGGATGAAGGATA[C/T]GGACACTTTTCAAAA | 23092 |
| rs185108665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790184 | ATAGTGTAAAGTACC[A/G]TGATGGAAATGAGAT | 23092 |
| rs185123694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052651 | CCCAGTATGTGTCAG[G/T]GGAACACACGGAGAG | 23092 |
| rs185130336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180569 | TTGACTTACAGTTCC[A/G]CATGGCTGGGGAGGC | 23092 |
| rs185139139 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809083 | GCTTGGTTTTCAAAG[A/G]ACTTAGTTGAGTGCA | 23092 |
| rs185141055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216352 | GAGTGATCTTTGAAA[A/G]ACGGAAATGGCATTA | 23092 |
| rs185145235 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142333 | TAGTAGAGATGGGGT[C/T]TCACCATACTGGCCA | 23092 |
| rs185148180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011716 | AACCATGATCTAGCT[C/T]AAGTTCATTTATATA | 23092 |
| rs185150829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013693 | TGCCCAACAGAATTG[C/T]CATGTTGATGATTTC | 23092 |
| rs185157649 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992281 | GTTTTGGCATCAAGA[C/T]GTAAGGTGAAGACCA | 23092 |
| rs185164436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978951 | AAAGCAATGCTAGGG[C/T]AAAGGAAAAAGGAGG | 23092 |
| rs185168008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975697 | GTACCTAAGATTGCA[C/G]TGTGTATACTTGTGT | 23092 |
| rs185171357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220978 | AGTCATTTAATTAGC[C/T]CAGGAAGGGAATAGG | 23092 |
| rs185178894 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789108 | AGCCCTTAAATCTTC[C/T]GTTTTCTCATTTACA | 23092 |
| rs185185269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939368 | AGGCTAAGGAAAAAC[C/T]ACTCCTCTAGTAAAA | 23092 |
| rs185185983 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812447 | GGTTCAAGCAATTCT[C/G]GTGCCTCAGCCACCC | 23092 |
| rs185190260 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770380 | TTCGAGCGGCCCAGA[C/T]ACCGGCGGGGCGGCC | 23092 |
| rs185219984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853736 | GTAGCCTTGACTCCA[C/T]GTTCTCAGATGCTGT | 23092 |
| rs185220111 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877000 | TGCCTAAGAAAGGGA[A/T]ATGATTCTTTTGAGT | 23092 |
| rs185224264 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896558 | TAAATGGGTTTTCCT[C/T]CTCCTTCTTCTCCTT | 23092 |
| rs185228064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153793 | CTGTCTTAACACACA[C/T]GCTCATGCATTTCCA | 23092 |
| rs185231484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888633 | AATTCCAGCCCATCC[C/T]TAGATCCCTGGAAGT | 23092 |
| rs185237216 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916081 | TGTGGAAGTGAAAGA[C/G]GGGATGGTTATATTT | 23092 |
| rs185241785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934698 | AGGGAGCTGTTATAG[G/T]GGCAACTATTTCCTG | 23092 |
| rs185245244 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224159 | TGATTTGAAATACTA[C/T]ATGGCAAAGTTTTAT | 23092 |
| rs185251341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955600 | ATATCACAAACCTCC[C/T]GCCTCAATCATTGTA | 23092 |
| rs185254025 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199205 | AAAGAACACGAAACA[A/G]TCAAGCTCAGGGACT | 23092 |
| rs185256885 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217263 | ATTCCAGGGGCCCCT[A/G]CTGTGACTCTGGAGT | 23092 |
| rs185269175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116613 | TTACAAGCCCTACAA[C/G]GGTTGGCTACTGCTA | 23092 |
| rs185271876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823975 | TAGACAAATAACAAA[A/G]CAATGGATGAGTACT | 23092 |
| rs185275656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121918 | GGAATCTAATAAAAA[A/T]TGCTGTTTCTCTTAA | 23092 |
| rs185278239 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158953 | AAGAAACTTTGGTGC[A/G]TTCAAAATAACATAA | 23092 |
| rs185291028 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844114 | TAGAGTGTAGTGGCA[C/T]GATCTCGGCTCACTG | 23092 |
| rs185295429 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214411 | GATCATACACATCAC[A/G]TGTTTAAAATGGTAC | 23092 |
| rs185306837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793649 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 23092 |
| rs185314234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828580 | TGCTTTCATTTTCCT[A/G]ACAATTAGTTGTAAC | 23092 |
| rs185322998 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178402 | AGAAGAAGGAGCATT[C/G]TGTTCATTGTATGAG | 23092 |
| rs185331618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156549 | TGGAAGGAGGGCCCT[C/G]CAATCTGTGTTTTAC | 23092 |
| rs185335634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196738 | TGTGGTACTAGGTAG[A/G]CCTCAAACAGACACT | 23092 |
| rs185341343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869533 | GACTGAGCAGCAAAA[C/T]ATTTCAAGGGTAGTT | 23092 |
| rs185355774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173606 | AGTCACTTCTGACAG[A/G]TGGGTATTGTTTTCC | 23092 |
| rs185371996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097274 | CGCTTGAACCTGGGA[C/T]GTGGAGGTTGCAGTG | 23092 |
| rs185376214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135123 | TTAGAGATATACACA[G/T]TGAGAGAGGTAGCAG | 23092 |
| rs185379762 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094595 | AAGGCATGGTACCTC[C/T]GTATAGAAGGATGTG | 23092 |
| rs185391684 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053997 | TCTTCTATCGTTGGA[C/T]ATTTAGGTTGTCTCC | 23092 |
| rs185397616 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077909 | GAGCATATCTCCCCT[C/G]CCCCAACCCTGGTTT | 23092 |
| rs185407523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032872 | GAAAAAGAAGAGACA[A/G]AGAGAGATGGGGGTC | 23092 |
| rs185410681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989974 | TTTGTGGCTTTCTCT[G/T]TATTTCCTGAATTTG | 23092 |
| rs185449219 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786075 | TTCTGGGCACAAGCA[A/G]TCCTCCCACCTCAGC | 23092 |
| rs185459249 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805000 | TTTTCGGGTCCATTC[A/G]TGTTGAAGCATGTGT | 23092 |
| rs185467028 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080848 | ATGAGCTGAACAGGA[A/G]CTAGTGTGGTGTTGG | 23092 |
| rs185471513 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011056 | GGTCACAAGGCTCTG[C/T]AGGATCGGATTGCTG | 23092 |
| rs185500305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885221 | TGTTCTGAGCAGAAG[A/G]ATCTTGAGAGATGGA | 23092 |
| rs185506601 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789382 | CCTTGTACTCTGGCC[A/G]GTATTATATTGAATT | 23092 |
| rs185538758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825642 | AATTCCTTAGCGGGA[C/T]GATACATTCCTTCTG | 23092 |
| rs185543924 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954306 | TGCTTTCTCTGCTCC[C/T]GTGGTCAGAATTTTA | 23092 |
| rs185548099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865023 | CCTCTCAAAATGGGT[G/T]TCTTTGTTTTCATTA | 23092 |
| rs185549392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872880 | AGTCAGAAGAGGAAG[G/T]CCAGGTGCTATGGGC | 23092 |
| rs185566710 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891997 | TCCCTGGGTGCCAGA[A/T]CCCAGATCAGTGGTT | 23092 |
| rs185570325 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987129 | TTCCTATCCATGAGC[A/T]TAGAATGTTCTTCCA | 23092 |
| rs185570743 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912284 | ATAGCAAAGCAATTA[C/T]GTTAAGTGAAAAAAG | 23092 |
| rs185582634 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929282 | CTCCCCTGCCCTGCC[C/T]ATTTTTTGCTATGAA | 23092 |
| rs185588946 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952476 | AACATCCTATGTACC[A/G]TAGTGTGTCTGCAAA | 23092 |
| rs185596950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027693 | CCATATGCCAAAGTG[A/G]AACAATCCAGCATTC | 23092 |
| rs185608474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015929 | CTTTGGAATCCTTAA[A/T]AAAGTGACCACCCTC | 23092 |
| rs185610059 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056378 | GATAGAGAAAAACAA[A/G]TTTGCCTTTCTAGTT | 23092 |
| rs185610896 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971459 | GCCCTGGATTAGCTG[C/T]TATCTCCTCAGCTGG | 23092 |
| rs185611494 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801773 | GCAAGGAATAGGGAC[A/G]AAAGTACCTTGTCTT | 23092 |
| rs185611519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851736 | CCTTTCTCCCACGTG[C/T]TGGCCTTTAGTTGCT | 23092 |
| rs185614340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991928 | AGACTGTGCCAATTT[A/G]TACTTCCATGAGTTG | 23092 |
| rs185619233 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827162 | CTAATGAAAAGCCGG[A/G]AGTTGCTTGGTGAGA | 23092 |
| rs185619617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866800 | TCAGAATGCATGTTA[C/T]GTAACGTACCGTGGC | 23092 |
| rs185619902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995612 | AGTGTGGTGATTCTT[C/T]AAGGATCTAGAACCA | 23092 |
| rs185629372 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820229 | TCAGGAGACCCCAAC[A/G]TTGAGAATTCAGTTC | 23092 |
| rs185633676 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887210 | GTCCAGCATTTTCTT[G/T]TAGGGCTGTGAATGT | 23092 |
| rs185639419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906612 | CTATAATTTATAACT[C/G]TCCTTATTTATCTTG | 23092 |
| rs185650210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924863 | CTTTGTGGATGACCT[A/G]GAGATACTCTCCTGA | 23092 |
| rs185653692 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167731 | GTGCTGGGTTAAGAA[C/T]TTGTCTTGCCTACCA | 23092 |
| rs185662924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946153 | TGCATCTTCTAAAGC[C/T]TCTCTGACATATATT | 23092 |
| rs185668865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966121 | TACAGAAAAGAGTCA[A/G]ATATTGACACACACA | 23092 |
| rs185684671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850021 | CCCCAGCCAGAGCCA[C/T]CTCACTTGGATCTTT | 23092 |
| rs185693074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094325 | GTGAGGATCCTTTAA[A/G]CTAGGTTGCTGGTCA | 23092 |
| rs185696962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908737 | ATTGTAGGAAAAGCA[C/G]GTGGCATAGAAGGTG | 23092 |
| rs185697209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130868 | AATTTGCAAAAGCAC[C/T]CTGTACCTTGGAAGA | 23092 |
| rs185698260 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004979 | AGGTAGAAGGAATGG[G/T]AAATTCAAGGATGAC | 23092 |
| rs185705543 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880346 | AATATGGCGAAACCC[C/T]GTCTCTACTAAAATA | 23092 |
| rs185711877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968841 | CAAACTGCTGGCACA[C/T]AATAGATGCTCAACA | 23092 |
| rs185717845 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949453 | TATTGTCCTTTTGCT[A/G/T]TTCTTTGGTTGGGGC | 23092 |
| rs185724216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989063 | TTAACTTTCTGCCTC[A/G]TTGATCTGTCTAATG | 23092 |
| rs185728468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053106 | GTTGTCGGACTTTCA[A/G]GCTCTGTGTGGTGGC | 23092 |
| rs185734503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970768 | AAGTAGAAACAAGGA[C/T]CACTACAGCAGTAAT | 23092 |
| rs185760407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071077 | AATATACTACAAAGC[A/T]GTAGTAACCAAAGCG | 23092 |
| rs185779356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002461 | TTTCTTTTGGGAGGA[C/T]GGGAGGTGGTCTCTC | 23092 |
| rs185780502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863459 | CTCTCCCTAGGTTCA[C/T]ATGTATAGTTGGTGG | 23092 |
| rs185781447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028077 | CAGACTGAGTTAAAT[A/T]AAATCTTGGTTCCAC | 23092 |
| rs185786538 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880892 | CAGTTTGAAAGAGGG[A/C]CTGTGGCAAAGACTT | 23092 |
| rs185789503 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901199 | TAAGTATATGAAGCC[A/G]TGTGGTGAGCATTGT | 23092 |
| rs185793073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967231 | ACATATGTATAAAAA[C/T]AAGTGCCAGTAAGAC | 23092 |
| rs185793528 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951163 | CTCCCAGGTTCAAGC[G/T]ATTCTCCTGCTTCAG | 23092 |
| rs185798666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151192 | GTCTTATGTCTTCAG[A/G]GAAATACAAATAAAA | 23092 |
| rs185803719 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922297 | AAAAAGGATCATCTT[A/T]TGTAACAGACTTTGT | 23092 |
| rs185807137 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941130 | TTGGGTATATACCCA[A/G]TGGGATTGCTAGGTC | 23092 |
| rs185810629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090753 | AAAAACCTGTTGGCA[A/G]TTCATTCTTGCTCTT | 23092 |
| rs185829729 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889989 | AAAAATACAAAATTG[A/G]CCGGGCATGGTGGTG | 23092 |
| rs185831840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112632 | CCCTTTCATCTGGCC[C/T]CTGGCAACCATCTTT | 23092 |
| rs185832685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071834 | TGCTTGAACCAGGGA[G/T]GGGGAGGTTGCAGTG | 23092 |
| rs185836116 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075280 | AAATATTATGTATAG[G/T]GATTTTAGTTTCTTA | 23092 |
| rs185840075 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927071 | AGTTGCTAGTCTGCC[A/G]TGGTTATACATCTAG | 23092 |
| rs185840840 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028264 | GTGTTAGCCACGGTT[A/G]TCATTGCTGTTGTTA | 23092 |
| rs185842254 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050683 | AGACTTTGAAGACTG[G/T]AGCCTACTGGAGTAG | 23092 |
| rs185856569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012151 | TAGACAATCCTCTTT[A/C]AGTACAGAAACCTGT | 23092 |
| rs185864624 | snp | A/T | 0.00120024 | 0.0244679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992445 | TTTATTTTTTATTTT[A/T]TTTTTTGAGAGGGAG | 23092 |
| rs185865371 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032533 | GATTAAGGACAGCCG[C/T]CTCCATCTGGCGAGC | 23092 |
| rs185882383 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177487 | CTGGCAGAGCTGGCA[A/C]GTCAGTAGCAGACAC | 23092 |
| rs185894887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926235 | TTGGGTAGCAACTTG[C/T]CCTGTAATAGATGGA | 23092 |
| rs185897010 | snp | C/T | 0.000231965 | 0.010767 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214128 | GATATGGGCGGGGGG[C/T]GGGGGCAAGGGGAGC | 23092 |
| rs185899834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049735 | TTGTACATAATTTGA[A/G]CCAACTTTCTGGTAT | 23092 |
| rs185901595 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020184 | GACTCCTGGCCTCAC[A/G]TGATCCTTCCATCTT | 23092 |
| rs185913710 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986096 | CACTGTCTTCCACAA[C/T]AGTTGAACTAGTTTA | 23092 |
| rs185943310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147116 | TTGTTTCTTAAGCTT[C/T]CCTGGGATCAGAGAT | 23092 |
| rs185945053 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059214 | CCTAGCATGTGTGGG[G/T]ATGCTCATGACTGCT | 23092 |
| rs185947149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038656 | AATCACTGACAATGC[A/G]ATGGAAATACATTTT | 23092 |
| rs185951328 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108719 | GAGATAGGTTACCTA[A/G]GGTGGGTATTTCATG | 23092 |
| rs185952878 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844770 | GGAGGCAAGAGAATC[A/G]CTTGAATCTGGGAGG | 23092 |
| rs185953134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019169 | ATCAGTGACACCAGA[C/T]TCTCTAATTTGTCAA | 23092 |
| rs185960652 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824138 | CAGTATGTTGTGTGT[A/G]TGTGTGTGTGTGTGT | 23092 |
| rs185981074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122993 | TCCATTGGCTTTCTG[A/G]CCTCTTCAAGCATGT | 23092 |
| rs186015544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088513 | TATTTTCAAGGTAAG[A/G]ACCTCCTATAACATT | 23092 |
| rs186021280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045046 | ACTGGTTTGCTAATC[C/T]AAAAAAGAAGCACTT | 23092 |
| rs186025585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780179 | CTACATTGGTACATA[A/G]AGAGCTCACTCATTG | 23092 |
| rs186026656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207999 | CCCCCATATACTCCC[G/T]AAACCATCCATGCTC | 23092 |
| rs186033178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196220 | GCCTTGCTGGTGTCC[A/G]CATCTCTTGCTTTCT | 23092 |
| rs186037474 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947627 | ACATAATAAGCACCT[A/G]TTACTCACTGAATTA | 23092 |
| rs186039504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819702 | GATAATTATATGCTG[C/T]ATTTGGAAAACTTAT | 23092 |
| rs186043183 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226211 | CCATGGCCGGGTGCA[A/G]TGGCTCACGCCTATA | 23092 |
| rs186047923 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007441 | AATTCCTGTTATGCT[A/T]AAATTGGGTGGAAAT | 23092 |
| rs186048897 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152203 | TAGAACACAAAGACT[A/G]AATGCTAATGTAAAC | 23092 |
| rs186054006 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859963 | CCCTCAGGGCTGTCA[A/G]CGTTCCCCCTTACTC | 23092 |
| rs186055259 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131612 | GACACCAGCTTTTGT[A/C]GTGAAGATTGCCTGG | 23092 |
| rs186061467 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168856 | ATGCCTGCTTATTTT[C/T]ACTCCTTACACAGAG | 23092 |
| rs186061950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126711 | TCCTTACCGTGGACT[C/G]TCCTTGAATTATATG | 23092 |
| rs186065381 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105453 | ACCTAAAGACCAAAC[A/T]GACATTAGCTAATGT | 23092 |
| rs186074355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114680 | AATTGGTCATCTCAG[A/G]CCTACCCCAGCACCT | 23092 |
| rs186093568 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095083 | ACCTGGACTTTTGAC[A/T]TATGGGTTCTAAGAT | 23092 |
| rs186097718 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148831 | ATTTTCTGTACCTAG[C/T]AGTTGCTGAAGTGAT | 23092 |
| rs186104772 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227739 | AAGCACCTGTATTAT[C/T]GAGAGGAAAAAGTGT | 23092 |
| rs186106444 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128580 | AGTTACAATACATAA[A/G]CCCTGCTAAGACTTG | 23092 |
| rs186106602 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213072 | ATGGCGTGAACCCAG[G/T]AGGCGGAGCTTGCAG | 23092 |
| rs186114526 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165838 | TTCTATTTCTGAGTA[C/T]GACGAACAGTTCCTT | 23092 |
| rs186122065 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109772 | AATGTTAAGCAACCT[A/G]TGGAATTTCAGCATT | 23092 |
| rs186126678 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143651 | ATAAATTTTTGACTG[C/T]GTATTATTCCCTTAT | 23092 |
| rs186128584 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104503 | GCGAGAGAGTGAGAA[A/C]CTGTCTCAAAAAAAC | 23092 |
| rs186134436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181032 | CTTCTCAACAATGAT[C/T]AAGACCTGTTGATTC | 23092 |
| rs186138960 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091784 | TGCTTTTATTTTAAT[A/T]TCCAGTTCACGGAAA | 23092 |
| rs186144557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159256 | ACCCAACAGGAAGCC[C/T]GAGGTTGCAAAAGCC | 23092 |
| rs186154040 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065361 | ATGAGTGTTATCTGC[A/G]ATACTTATGTTCTTA | 23092 |
| rs186155844 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800861 | AGGGTGGGAGGAAAG[A/C]GGAGGCCGTGGCAGA | 23092 |
| rs186159217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001710 | TGCAGAATTCTAGAA[C/T]CTACAGTTCCATTTT | 23092 |
| rs186160109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838129 | GGGCATAGTGGGTGG[A/G]CACCTATAATCCCAG | 23092 |
| rs186160187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024542 | CAGTGCAAGGGGTTA[C/T]TGAGACAGAGACTAA | 23092 |
| rs186178223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966590 | GCCATATAGCCATGA[A/T]AGACTTTGTTGTTTA | 23092 |
| rs186194046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900904 | CCTTCAGAAGCCGAA[A/G]TTAATGGGATAGTCC | 23092 |
| rs186212262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940515 | ATGTCCATGTGTTCT[C/T]ATTTAGCTCCCACTT | 23092 |
| rs186214060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203400 | CCAGTTAGAATGGCA[A/G]TCATTAAAAAGTCAG | 23092 |
| rs186249576 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165007 | GCTTTGCTTTACTTC[A/G]GATTCATATAGAAAT | 23092 |
| rs186265906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203526 | TGGCGATTTTTCAAG[A/G]ATCTAGAGCCAGACA | 23092 |
| rs186272862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185392 | ATAGCTAGAAACAAC[A/G]AAGTTTCTTTCTGTA | 23092 |
| rs186275318 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980294 | TAATTATTCATTCTT[C/T]GATTGAACAATGGAT | 23092 |
| rs186278465 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209313 | GACTGTTTTTCCTTC[C/T]TACTTCTTCCTACCT | 23092 |
| rs186290423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837031 | CCCTTTAAATCTCTC[A/G]CAGAACGCATTTGGA | 23092 |
| rs186294142 | snp | A/T | | | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859553 | ACAATGCCAATTTTC[A/T]ATAAGATCATCTGAC | 23092 |
| rs186294633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876073 | TCAGCATTAGCAGAT[A/G]AGAGATTCCACATCT | 23092 |
| rs186296609 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895529 | GCCAGCACGCCCGAC[C/T]AAGAAAGGAGACTTT | 23092 |
| rs186299903 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226705 | TCTGAAGTATTTATA[C/T]GGCCAATATGTGTTT | 23092 |
| rs186332287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208430 | TATGAAGCCGAGTTT[A/C]ACTTTTAGAAGAAAA | 23092 |
| rs186337711 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880686 | AGCTGCGGTCTCTTA[C/T]GCCACCTGCAGGGGC | 23092 |
| rs186348569 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856295 | AGGTGGCAGTCGGTT[G/T]GTTGTGTTGGTCAGG | 23092 |
| rs186355178 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921562 | AACTGAAGATTGGTG[A/G]AAGTCAGAATAGTGG | 23092 |
| rs186364884 | snp | C/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956246 | ATTTTAGGACATCTT[C/G/T]TCTGTGTCCTGGTCT | 23092 |
| rs186373514 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221914 | TGGGCAGGTGGGTGG[A/G]TGGATGGATGGAAGG | 23092 |
| rs186373753 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961748 | TCCCACAAGGAAATA[G/T]GTTGAAAATATTCAA | 23092 |
| rs186387053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122293 | CCTTGCTGTTTCTTG[A/G]ACACCACAGGCACAT | 23092 |
| rs186393322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142573 | TTTTAAGTTTGTTTT[C/T]ATCATAGGGACTGAG | 23092 |
| rs186394757 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086392 | TTGCCAGCACACTTG[G/T]TTGGGTTCCTGAAGA | 23092 |
| rs186398423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148054 | CCCCACATTGCTTCA[C/G]ATGCTTCCTTAGACT | 23092 |
| rs186402163 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034367 | TCTATCAGCCGATGA[A/G]TGGATAAATAAAATG | 23092 |
| rs186405799 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184839 | GGAAGGAACGTGTGT[A/G]AGGCCAAATTGCCCC | 23092 |
| rs186406093 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103799 | GGGACCTAACAGGGG[C/G]TAGGGGGAAGAGGAG | 23092 |
| rs186414632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017521 | TTCATTCATTCTTTC[A/G]TTTCATTTTATTTAT | 23092 |
| rs186416000 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064759 | TTTGTCTGTTCTGTG[A/G]CTTTGTAGCCTTTAG | 23092 |
| rs186420290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800232 | GGGGAACTAGGGAGG[C/G]CTCTAGAGACATGCA | 23092 |
| rs186420509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997420 | TTCTTTTCTTGAGGG[C/G]TTGGTGGGGACAGGG | 23092 |
| rs186422250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044052 | TTTTTGTTGAGGAAC[A/T]TGAATACTGAGCCAA | 23092 |
| rs186426787 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982015 | ATCCATTTGACCTCA[A/G]GCTGCTTTTTTGCTG | 23092 |
| rs186432405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779321 | ATGTTTGTGTCTGGC[C/T]CATTTCACCTTGATT | 23092 |
| rs186433860 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819303 | TCAGAGGTCAACCAT[C/G]GTCCTTGCAGTGGGG | 23092 |
| rs186468494 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993524 | TGGCCAGGCTGGTCT[C/G/T]GAATTCCTGACCTCA | 23092 |
| rs186471409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977289 | TAACACCTCAACCCG[C/T]GGTTCTTCCTTGAGA | 23092 |
| rs186476195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127854 | AAACAGTTGTTGATA[C/T]GCAAAATTAATAAAA | 23092 |
| rs186492559 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809310 | GAAAAGAAAAAAATA[C/T]AGGTCTACTGTAAAT | 23092 |
| rs186516528 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018762 | TCTTAATATCTAGTT[A/T]TATAAGTCTCCTCTA | 23092 |
| rs186516558 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839115 | ACAAACATTTCAGAC[A/G]ATTCTTATGTATTTT | 23092 |
| rs186527010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877351 | TCTTAACATCCAGTT[C/T]GTGCTTCTGATCCTG | 23092 |
| rs186528311 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985661 | CCCTCCCCCCTCCCC[A/C]CCACCCTACAACAGG | 23092 |
| rs186532748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916760 | AAAGGCAAAAACAAC[C/T]ACCACAATAAAACCC | 23092 |
| rs186534985 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795361 | TGACTCTTTACCACC[G/T]CACAGCATGCTCTAG | 23092 |
| rs186543083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774779 | AACCACTAATCTTTT[C/T]ACTGTCTCTCTAGTT | 23092 |
| rs186548388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034134 | AGAAATTGGAACCCT[C/T]GTACATTGCGGGTAG | 23092 |
| rs186551165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814872 | CTGTAGACAATGCTC[A/C]ATAGTTATTAGCCAG | 23092 |
| rs186559912 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855620 | AGACACTATTCCTTC[C/T]TTCTATCCATCCTCA | 23092 |
| rs186560204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831891 | AGCTACCTACATAGC[C/T]GCTTGACTGACTCTT | 23092 |
| rs186564689 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872112 | CTGGGGATTGGATTT[A/G]TATCCAGTGCCCCCA | 23092 |
| rs186565233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935640 | TAACTACTTGGTCCA[C/G]AGGCTAGGATGGATG | 23092 |
| rs186574312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996119 | CGGGTGCAGCAAACC[A/G]ACATGGCACATGTAT | 23092 |
| rs186577778 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891355 | AGATTGGTTTGATCC[A/G]GCAGTTACTCAGCAG | 23092 |
| rs186612120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898086 | AAAGAAACAGTTGTA[G/T]TATTCCCAAGGAAGA | 23092 |
| rs186622750 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918389 | TGACCTCAGGTGATC[C/T]GCCTGCCTCGGCCTC | 23092 |
| rs186625806 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937359 | ACTATGAACTATCAC[C/T]TTCTAGAATGACTAA | 23092 |
| rs186633509 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957502 | ATTCACTTTGTGGCT[C/T]GTCTTTGTACCATTG | 23092 |
| rs186646350 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029558 | CACAGGTTCACACCA[C/T]CATGCCCAGCAAATT | 23092 |
| rs186647864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013156 | CCAATTAAGCTAAAT[A/G]TCAACCTCTCTTAAA | 23092 |
| rs186650708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133203 | ATGAACTTTTAGAAG[A/T]ATAAAAGCCCCTCCT | 23092 |
| rs186653065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217415 | AAGAGCACCTCAGAC[A/G]GTAACTGGAAAGAGA | 23092 |
| rs186668371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115766 | CATATTATTGCTCCC[A/G]TTTTATATGTGAGGA | 23092 |
| rs186669854 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152759 | AACCCAGTCACCATG[C/T]AAAGAAGCCTGTTGT | 23092 |
| rs186671013 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928466 | ATTTAATCCCGTGCA[A/G]GAGCTCACTAAGGTG | 23092 |
| rs186675479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791221 | CTTGGATAAACCAGG[C/T]GTAACTGCTCTGATA | 23092 |
| rs186685221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095927 | TCAGTCCTAGCATAT[A/G]CATATAGTCGGAAAA | 23092 |
| rs186685941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852960 | TCTCTTTTGCAGAGG[A/C]CTGCTGCTTTGAAAC | 23092 |
| rs186686523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144407 | TTTTTCTTTATTATT[A/G]TTATTATTTTTTAAA | 23092 |
| rs186690401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181961 | CGACTTCCCCTGACA[C/T]GGCTGCCTCCCTGGC | 23092 |
| rs186690698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055670 | CGCTGGGAAGATCAA[C/G]ACTTGCAAATATGTA | 23092 |
| rs186695109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143009735 | TAACAAATCTTCATA[C/T]ACAATGGTCAGTAGA | 23092 |
| rs186697657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962495 | TAATAATATGATAAC[A/G]GATACAGGGCATCTT | 23092 |
| rs186701552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141521 | AAATGCATATTTCTT[A/G]TATATTCACTTGGTT | 23092 |
| rs186703197 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186473 | GTACTGATTCTTCCC[C/T]ATCTTCCCAGGCCTA | 23092 |
| rs186703551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991240 | GGTGAGCAAGGCTCC[A/G]TGGGCGTGGGACCCT | 23092 |
| rs186704699 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179416 | TTGGACCAGCCTGGG[A/G]TCTCCTGGGTTGCGT | 23092 |
| rs186708995 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222853 | GGGTGAAGAAATTGG[C/T]GCTGAGATCCAGGCT | 23092 |
| rs186710182 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034778 | AAAAAAAAAAAATTC[C/T]TCCCCTGGATTCCAA | 23092 |
| rs186713724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017896 | GCATTGCTGGACAAA[A/G]GCTATGCATATACTT | 23092 |
| rs186717888 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203927 | CTGTCAGGGGGTAGG[A/G]GGCTAGGGGAGGGAT | 23092 |
| rs186719456 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157775 | CACAAATAGCTTTCC[A/G]AAGACTGAAATGGGT | 23092 |
| rs186719500 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868373 | GGACTTTCGTCTTCA[C/T]CTCCAGAGCTCTGGG | 23092 |
| rs186730192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860451 | TAGGACTGTAGTCCA[A/G]GAGTGCTTGGCTCTC | 23092 |
| rs186730515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038127 | GATTTGATTTGAACC[A/G]TTGTCAGAGATGTGA | 23092 |
| rs186737250 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976152 | GTATCATCATATTCT[A/G]TTTCACTTCATTGGA | 23092 |
| rs186738821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084037 | GCTCTCGCCGTCCAC[A/G]TCATTGACTTTTATA | 23092 |
| rs186742334 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101759 | CTTAATGGAAATGTC[A/G]ACATTTCAATTTCTG | 23092 |
| rs186748964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001020 | TGCATGTTCTGCACA[C/T]GTATCCCAGAACTTA | 23092 |
| rs186749498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078825 | TTAGAGACTTTCTTA[A/G]CATCTGAGCTCTTTG | 23092 |
| rs186758159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897011 | CTGTTTTAATATAAA[C/T]AGTTTTGGTAGCTTT | 23092 |
| rs186759081 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195551 | CATCAGAGACATCCT[C/T]CTTGACGTCCCCCTA | 23092 |
| rs186763796 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954036 | ACATGATATATGGCA[C/G]GCAAGTATGCTGTCT | 23092 |
| rs186768996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055218 | TAAAAGGAGAGGGGA[A/G]TGGTCATCAGAAATA | 23092 |
| rs186793651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117830 | CCAAAAATCATTTGA[A/C]GTTTAATGAGTAAGT | 23092 |
| rs186795328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016618 | TGAGGCAGGAGAATC[G/T]CTTGAACCTGAGAGG | 23092 |
| rs186800674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155510 | TTGGTTATTAGTGGT[A/G]GTTCTTCTTTTTTAA | 23092 |
| rs186806733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051535 | GATGCCATCAGGAAG[A/C]TTTTGTAAGTGAGGG | 23092 |
| rs186810389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787064 | GAACAGCACTGTCTA[C/G]GGCTCCCTTTCCTGT | 23092 |
| rs186818784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980608 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 23092 |
| rs186839628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814260 | ACCATGGCTAGAGCC[C/T]TCCGGTAATCTGCAA | 23092 |
| rs186839832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081822 | TTCGAGACCATCCTG[C/T]CGAACACAGTGAAAC | 23092 |
| rs186850435 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769281 | AACATGAAGCCCCCA[A/C]GTAGCTGAAGGAGGG | 23092 |
| rs186866992 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890936 | GTCAATTCTGTTTTC[C/T]TTATAGGGATTTCCT | 23092 |
| rs186871351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792484 | TTCTCTATTTTTGCT[C/T]ACACAGATGCCCTGT | 23092 |
| rs186876205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201270 | CCCAGGAATATTTAG[C/G]GGCACTGGGCATTCA | 23092 |
| rs186877250 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910494 | CTGTTAATCCCAGCA[C/T]TTGGGAGGCTGAGGC | 23092 |
| rs186879472 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828223 | ATCTGTTAAAAATTA[C/T]GAGTGTTGTCCTCTT | 23092 |
| rs186882779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110573 | GACTGGCATACACAT[G/T]TGCAACTTTTAAACC | 23092 |
| rs186886370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811144 | GTAAAAATAGACCTA[A/C]CTCCTGGGGTTATTG | 23092 |
| rs186889292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159880 | GATCTGTGGCGGAAG[A/G]AACACTGCCTTTTCA | 23092 |
| rs186890081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129800 | CTCATGCCTACTCTT[G/T]GCCACATACTGCACT | 23092 |
| rs186895433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092718 | ACCTTTTAAGTTTGG[A/G]ATTTCAATTATTCTT | 23092 |
| rs186907592 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139022 | GTTGTGACCTAGTCC[G/T]CGAACTCTTCCTTAT | 23092 |
| rs186913747 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074171 | CTGACTTCCTTAGAC[A/T]TTAATTAGTTAATTA | 23092 |
| rs186922955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123655 | CCAAGAGTTTGAAAC[C/T]AGCCTGGGCAAAATA | 23092 |
| rs186942494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202223 | TTTTCATCTTTGTTG[A/G]TTTTAAGTGTTTTAT | 23092 |
| rs186948804 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182654 | TAGCTAATTGGCCTA[C/G]GAGATAATTCACATA | 23092 |
| rs186955882 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219410 | TTGTGGAGCCAGGAA[A/G]TGCTATAATCCAAAC | 23092 |
| rs186968306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222302 | CACACACACATCTGC[C/T]GCCTGCTCTATCTGT | 23092 |
| rs186976192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176865 | CATAATCTCAGAATC[C/G]GTAAATGCCTTTAGG | 23092 |
| rs186990523 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791660 | CTCCTCCCTACCCCT[C/T]GCATTTAAAAGGTGT | 23092 |
| rs186995128 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827243 | CTCCATGGTTGGTTG[A/T]GGCATGGCCCTGTGT | 23092 |
| rs186996579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137719 | ATTCCATTTGTCAGT[C/G]CTCTCTCCAGTCCGC | 23092 |
| rs187006838 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867505 | AAGCACAGTTTCTGA[C/T]TGGATATGTTCTCAG | 23092 |
| rs187016126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824816 | GCACCAAGAGTGCCA[C/T]GGAAGGGGCTAGGCT | 23092 |
| rs187021287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788845 | TAGAATATCTCCACC[A/C]TTTAAGTGTTTTCTG | 23092 |
| rs187023922 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098199 | CTTGACATATTTGAC[C/T]ATAAGTTCTAATGTT | 23092 |
| rs187025949 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794805 | AATACCCCGGCCAAT[A/G]ATTGACTGCCCTGTA | 23092 |
| rs187027948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073077 | TAGTAATAGTTAAAT[C/G]TGATCTTAGCTGAAA | 23092 |
| rs187029127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807257 | ATTCCTTTTTTGTGA[A/G]AAGCAACTTAGGGGC | 23092 |
| rs187029964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028621 | TCCCAGTTGCTATAC[A/G]TTTCATTTGACCCTC | 23092 |
| rs187034212 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907039 | GACTTGGCCAGAATA[C/T]GACTGCATGGCACCT | 23092 |
| rs187035276 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831239 | GTGCTCAGTCATTTG[A/C]TATCTCTCTGCCTCG | 23092 |
| rs187040052 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847413 | CCCGGGCTGGAGTGC[A/C]ATGGCGCGATCTCGG | 23092 |
| rs187049665 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806138 | TTGCTGTTTTGCCCA[A/G]GCTGGAATGCAAGGC | 23092 |
| rs187052060 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864361 | CGACTTGAGCTTAAT[A/G]AACTTCACAAAAAGA | 23092 |
| rs187062477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871745 | ATTTGTGTTCTGAGG[A/G]ATAGCCTCAGCCTGG | 23092 |
| rs187065177 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132217 | GGAGCCCGAGGACCC[A/G]CCAACCCATGGAGAG | 23092 |
| rs187080922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170233 | AGGACTGGCCCCTTG[C/T]CTTCTGTGAGAGCCA | 23092 |
| rs187087222 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209502 | ATAGTCAAGGCAGGC[C/T]GGGCACAGTGGTTCA | 23092 |
| rs187087400 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228846 | GTTCAGGCTTTTAAA[A/G]AATGCTTTTGTGTCA | 23092 |
| rs187089102 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199588 | GGGCAAAATCAAAGC[A/C]GCCCCCTGTTAGTTT | 23092 |
| rs187106422 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052582 | ACATCATACAGGTAC[G/T]GTGCCTTTGAGAGCC | 23092 |
| rs187110349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030629 | AAAGTGGAGGACCAA[A/G]AGGTTAAAAGAACTC | 23092 |
| rs187114125 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013394 | TTGCAATATGTCATT[C/G]TCTCTTTTATATTGG | 23092 |
| rs187139614 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780903 | TGACATCTCTCTCTG[A/G]CAGCTTCTCCTGCAG | 23092 |
| rs187177035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888369 | TATAGAATTAGAGAG[A/G]GGGAAGGACCTTAGT | 23092 |
| rs187177665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810214 | GGAGGGGTTCTTGGC[C/T]TTATCAGAGAAAGAA | 23092 |
| rs187185049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951534 | GCTGGGGTCTAATCT[A/G]GTCAGACTTTAGGCC | 23092 |
| rs187189278 | snp | C/T | 6.69591e-05 | 0.00578576 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907671 | GCATACAGTGGAATG[C/T]ATAGATATTTTATGG | 23092 |
| rs187194404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926489 | CCTTCTCTCATCTGG[C/T]GGGTGGAGGGAGCTC | 23092 |
| rs187200097 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948212 | CATATACTAAATGTC[A/C]CACCAGAGAAAGTCT | 23092 |
| rs187219734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851945 | CAGGGTTCACTCTAC[A/G]TAGGCACACAGTCCC | 23092 |
| rs187223872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915305 | GGTTCCCTCTGCATG[A/G]CGTGGAGAGATTTCA | 23092 |
| rs187227031 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887954 | TGGGCGACAGAGTGA[C/G]ACTCTTTCTCAAAAA | 23092 |
| rs187234525 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190509 | GCTGTCCACCAAGAA[A/T]TTTATGATCAGCAAA | 23092 |
| rs187237601 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216968 | GGCATTACAGAACAC[C/T]ATTATTCTGTCAGGC | 23092 |
| rs187267027 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152356 | TGTAAAACTTTCATG[C/G]AATTTTTCTGTAAAC | 23092 |
| rs187290009 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173372 | AACAAACCATTCTGC[A/T]GGGTGTGCAGGAGCC | 23092 |
| rs187293032 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153292 | TCTGGCATCGACATT[C/G]CCTGGCTGATGATAC | 23092 |
| rs187294282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816371 | AGTGAAGGCTGCAGC[A/G]ATAAAGCCTGCTCAA | 23092 |
| rs187302228 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192311 | GGTTACAGGAAAGGG[A/G]AAGGCATTTCAGATG | 23092 |
| rs187312874 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986403 | TTTGTAGATTCTGGA[G/T]ATTAGCCCTTTGTCA | 23092 |
| rs187314411 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095553 | TACATTTTTGTAAAT[C/G]TCCTTAATGTCTGAC | 23092 |
| rs187318210 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968026 | TTTCCTTGCTCATAG[A/G/T]TAACAGATCCGGAGC | 23092 |
| rs187319589 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134669 | ATACCAGTGTGTTAT[C/T]ACCACAATTATATCA | 23092 |
| rs187326513 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804515 | TTATTTTTTTGAGAC[C/T]GAGTCTCACTGTGTT | 23092 |
| rs187340410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869245 | AGCGTCTCACACTGT[C/T]GCCTAGGCTGGAGTG | 23092 |
| rs187343604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853593 | TAAAAGGGATTTAAA[C/T]AATAGTATCTACCTT | 23092 |
| rs187350015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843862 | CTGAGCTTTGGCTTC[A/C]TGCATTCTTAGGGCT | 23092 |
| rs187352229 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025043 | CCTTTGCTCAATGGT[A/G]CCTGGTATTATCGGC | 23092 |
| rs187352953 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055617 | ACCTACAAAAATCTT[G/T]TATAGTGTTTCTAGA | 23092 |
| rs187353555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008585 | TTTGGGTAAAGATGG[C/T]GCAGTTTAGAGAGGA | 23092 |
| rs187366055 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965272 | ATAACTGTGGGCAAG[A/C]CTGACTGATGTCAGG | 23092 |
| rs187368761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990479 | GTCAAAGTCATTCTC[C/T]GTCTAGCTTTGTTCC | 23092 |
| rs187375875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971947 | AGCATTTTGGGAGGT[C/T]GAGGCGGGCAGATCA | 23092 |
| rs187381315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023859 | TCCCTCCCTTGCCTG[C/T]GTTCCTTCCTGCCCT | 23092 |
| rs187395794 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989505 | TGTTATGCATGAATT[G/T]GATCCTATCATGATG | 23092 |
| rs187407490 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911759 | AAAGTGGAAGCTGGT[C/T]CATAGCCATTAAATC | 23092 |
| rs187458377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796573 | ACCTTCTGCTTTCAC[C/T]AAAACAGTTCTCAAG | 23092 |
| rs187459577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847736 | AGAGAAGCAGCACCT[A/G]TGTTGTATGGGTGGT | 23092 |
| rs187461295 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776237 | CTTGGCCTCCCAAAG[C/T]GCTGCGATTACAGGC | 23092 |
| rs187466366 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988746 | CTTTCATTTCGTTAT[A/G]TACCCAGTAGTCATT | 23092 |
| rs187467356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864602 | ATGAGGCAAAAATTG[A/C]TTAATTGTTATGGTA | 23092 |
| rs187479796 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884673 | TATCCTTGGAAGTGA[A/T]GTTGCTGCTGCTGCT | 23092 |
| rs187486314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903469 | AGATCTAAGGATTCT[A/G]TTAGGTTGATCTGGA | 23092 |
| rs187486968 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224161 | ATTTGAAATACTATA[G/T]GGCAAAGTTTTATAT | 23092 |
| rs187492317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088775 | ATATGTGATCCCTGC[C/T]GCTGTGTCGTTCCCC | 23092 |
| rs187494774 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923703 | CTTCAGTCTCTCATA[A/G]AAATGTAAGAACTTA | 23092 |
| rs187497853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167078 | ATAACAGCACAAGAC[A/G]GTATTGATTTTTATA | 23092 |
| rs187500342 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065463 | ATATGAAGTTAATCC[A/C/G]TGGGGCATAAGAGCA | 23092 |
| rs187500588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944204 | TACTCCTATACCTGC[A/C]CATCTAGAAATAAAC | 23092 |
| rs187515193 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045785 | GGTGGATCACCTGAG[G/T]TCAGGAGGTCGAGAG | 23092 |
| rs187516922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206613 | CTGCTGGTAATTGCA[C/T]GCCGTCTCCCAAGAG | 23092 |
| rs187520276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187658 | TTTGCCTGAGGTCAG[A/G]CGGAGCACCAGCACT | 23092 |
| rs187532056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150925 | AAACTTAAGTTGGAC[G/T]GTGTTTAAACTAAAA | 23092 |
| rs187536331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062394 | CAAAATGGACAAAAT[A/T]CTGTAGATCACTGGG | 23092 |
| rs187537366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821659 | AACTGGCATTTTAAC[A/G]AGATACCCAGGTGAT | 23092 |
| rs187537968 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130219 | TTGGTATTTATGGAT[C/G]TGCTAATTCCACTTA | 23092 |
| rs187539415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083158 | TTTCCCATTAGTCAC[A/G]GGTGTCATTGTTTCC | 23092 |
| rs187539990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861552 | TGCTGTGTGGACTGA[C/T]GGTGAGGAGGGCGAG | 23092 |
| rs187543324 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888244 | TTAACTCCAGCACTG[G/T]CTGTGCAGCCCTTTC | 23092 |
| rs187551643 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041534 | TTTTAGAACTCTTCA[A/G]ATGCTGCCTTTGGCA | 23092 |
| rs187551834 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229216 | GAGAATTTGCTCCTC[A/G]GGCATATTAAACAAT | 23092 |
| rs187554284 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022277 | GGGGTTTCACCATGT[C/T]GGCCAGGCTGGTCTC | 23092 |
| rs187556996 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149659 | AACAATCACCTGAGA[C/G/T]GACTTGGGTCTCAGC | 23092 |
| rs187557927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820962 | AGAAATCAAATTACC[C/T]GGGAAGGCAATGCCA | 23092 |
| rs187559174 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004301 | AGTCCTTCTCAGGCC[A/G]TATTTAGTTTGCTTT | 23092 |
| rs187563356 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110222 | CCATATATTTTCTTT[G/T]CTTATCGCCTGTCCT | 23092 |
| rs187565968 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802419 | GTAAGTCCTCACTTA[A/G]CATTGTCGGTAGGTT | 23092 |
| rs187567647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073755 | TATCTTAACTTGGGT[C/T]TTCTTCTCCTGGCTT | 23092 |
| rs187568837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840382 | TTTAGTAGGAAATAA[A/G]TCCTTAGTCTTTGTC | 23092 |
| rs187569382 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042075 | GCTGGGAAAGGTTCT[A/G]AGTAGGACTGGACAA | 23092 |
| rs187573252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793656 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT | 23092 |
| rs187573537 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142771536 | GTTCTGATTCTTGTG[C/T]TTAGCAGAAGGTGAT | 23092 |
| rs187578112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986961 | AAGCTTTGTTCTTTT[A/G]GCTTAGGATTGTTTT | 23092 |
| rs187585623 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968629 | AGGATTGCACTTCTT[C/T]TGTTATTTTATACAT | 23092 |
| rs187590107 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079218 | GGGCACAAAGGATCT[A/G]TAGAGTTGGGCAACC | 23092 |
| rs187596368 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785713 | ATGCTGAAATGGTGA[C/T]GTTTGGGGGTGTCAG | 23092 |
| rs187600596 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877707 | TCTCAATCATGGATG[G/T]CCACTGGAATAACTT | 23092 |
| rs187601937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860791 | ATGATTTAGAAGATC[C/T]GGCTTGCTCTGTGGA | 23092 |
| rs187610063 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089719 | TCTACATTTTTATTA[A/G]TTTTCACTCACCAAA | 23092 |
| rs187613003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823489 | ACCCTAAAGCCTGGC[C/T]CTTGGGACTGTGTGA | 23092 |
| rs187615816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863088 | GGAAAGGGGTTGGCT[C/T]CTTGGTTTTCAAGTG | 23092 |
| rs187617390 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047596 | AGGGAGACTATGCTA[C/T]ACCCCACATCTTTGC | 23092 |
| rs187621100 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897591 | TTAGTAAACCTTCCC[C/T]GTGATTCAGCTGCAC | 23092 |
| rs187624052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917229 | TTTTTAGTAGAGATG[C/T]GGTTTCGCCATGTTG | 23092 |
| rs187653966 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007431 | AAGTTTGTAGAATTC[C/T]TGTTATGCTTAAATT | 23092 |
| rs187665818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971309 | AAATAAAACTAGCAT[A/G]CTTTTGAAGAGAATG | 23092 |
| rs187666909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982996 | TGGTGGTTATTTCGT[A/G]CAGGTGACCTGAGAG | 23092 |
| rs187667013 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783005 | TTCCTATACCCCCGC[A/C]CCCACTCCCTTCCAT | 23092 |
| rs187670514 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928818 | TATAATTATTACTGT[A/T]CTTTTATTGTAGAGG | 23092 |
| rs187713603 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201740 | ATCAGAACTAAAATA[A/C]AATGTACTCTCTATT | 23092 |
| rs187744890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145236 | GAAAAGTAAATATAA[C/T]CACAGGAGAAATGTG | 23092 |
| rs187759567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182237 | CTATTCTGGAGGAAC[A/C]CAAAGCACTCGGCTT | 23092 |
| rs187759821 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874536 | TCAGGGCCATTGCAC[A/G]TAATGCTTATTGCTT | 23092 |
| rs187763053 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857370 | ATTCCTGGGTTGATG[A/G]GCACAGTGAGGCTGC | 23092 |
| rs187766878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922751 | GCAGTCCTACTTTTC[C/T]CTCCTGGTGCAACGT | 23092 |
| rs187769051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893530 | TCACTTCATATCTTG[C/G]CTGTTGTGAGTAGTG | 23092 |
| rs187770229 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160533 | CTCTGTTTCCCAGGC[A/T]GAGTTCAGTGGTGCA | 23092 |
| rs187773678 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803590 | AATCTCTGTGATGAC[A/G]CTTCCTTCAACCTCA | 23092 |
| rs187774338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125378 | AACACCCTCTCCCCC[A/C]AACCCAGAGAATCCA | 23092 |
| rs187774537 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106599 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGACTACA | 23092 |
| rs187775156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942103 | ACTAGAGTCAAAACT[A/G]AAGGGAAGGGTGGAG | 23092 |
| rs187776276 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162519 | TACATGTTAGTGATG[A/G]CCATGGCCAAGGTAA | 23092 |
| rs187780452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191294 | TGTAGACAAATGATA[C/T]CAAAATTAAGAGAGA | 23092 |
| rs187780874 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124519 | AGGTGGCCTCACTCC[A/G]CACAGCTGGGACTTT | 23092 |
| rs187783604 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963485 | CCACAATATAAGCAT[G/T]TTCTTTTCTCCACAA | 23092 |
| rs187784025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841801 | GAGTAGTGCCTGAGT[C/T]GTGTGGAAGGATGAC | 23092 |
| rs187785135 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089031 | AAAAAGGTTGCTTTA[C/G]GAGGAAGTTAAGTTT | 23092 |
| rs187785332 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914192 | ACTGAGTACTGCCTG[G/T]GGTTGCACTGCCTTC | 23092 |
| rs187799667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907278 | TGTGGGAAGCATGAT[A/G]TCATCGCAACAGATG | 23092 |
| rs187805422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795817 | CCCCAGAATCTCAGC[C/T]CTATTACCTACCACT | 23092 |
| rs187806231 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165915 | ACCTCCTAGGGTTGT[A/T]AGGATGAAATGAAAT | 23092 |
| rs187808245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878428 | ATTCATTCATTTAGT[C/T]GTTCAAATATGTTTG | 23092 |
| rs187810173 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833178 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 23092 |
| rs187810820 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129019 | ATGGGATTGAAGAAG[G/T]TCTAAAAATGTGTAT | 23092 |
| rs187820039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166874 | GGCTTTCTGCCATCC[A/G]GTATTTTGGGAGTAA | 23092 |
| rs187822702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205706 | CCTGTTACTTATAGG[C/G]TGGGTATCCTTAGAG | 23092 |
| rs187835825 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022356 | GGGATTACAGGCATG[A/T]GCCACTGCGCCTGGC | 23092 |
| rs187839690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092062 | AAATTATACAATATT[C/T]CTTGCATAAATTCCC | 23092 |
| rs187853350 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052138 | AATTTGCTGTGATAG[A/G]ACTCTATGGAATTTA | 23092 |
| rs187868184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902848 | GAAATCGAGATTGAC[A/G]TGCAGTGGGCTTACT | 23092 |
| rs187870511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100544 | TGTTTCTTGTACTTA[C/T]GGTATCACCTCTGAT | 23092 |
| rs187871228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107044 | CTGACATTTTTACTG[A/T]TGTATCTGTGTGTTA | 23092 |
| rs187881616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143068953 | TTCCCACTCTCTCCT[C/G]CTTGATAAGCTTTCT | 23092 |
| rs187882363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943404 | ATCAAATTTGGTGTC[C/T]AGTTAGGGCCTATTT | 23092 |
| rs187890968 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075598 | ATTTCTATTTTTAAT[A/T]AACTCCCAAGTGATT | 23092 |
| rs187905852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026186 | TTTGGCCTGTCGGCT[C/T]CTTGTGTTTTCAGCT | 23092 |
| rs187917521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797776 | AGTCTTTGGTGGTAT[C/G]ATTGATAATCTCCAA | 23092 |
| rs187932922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816856 | TGTGCTCAAGAAGAT[A/G]GTGTCCAGTGTGGTT | 23092 |
| rs187940667 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997963 | GCAGCAGAAATTGAA[C/T]AAGGTGATGTCTTTG | 23092 |
| rs187952259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834036 | TGTGTATGTTATATC[A/G]GGGTGCTTCTTGAGG | 23092 |
| rs187959032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964678 | CTCACCAAGTTTCAA[A/G]AAGACTAGGAAGGGA | 23092 |
| rs188002878 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068264 | TCAGACATCGCAAAG[A/C]AACCTCAAGGGCGCT | 23092 |
| rs188021390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142919194 | TAATGCGATATTACC[A/G]TTGTCCTTGTAAAAA | 23092 |
| rs188034805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220527 | GATCTTGGAAGCTTT[A/G]GTTGGATGGATGGGC | 23092 |
| rs188040208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145483 | GCGTGTCTTGTGAAA[A/T]GGAAAATTTTACTGA | 23092 |
| rs188048057 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172689 | AAGGTTGTTTTTACT[A/G]TGGTGCAACAAGGAG | 23092 |
| rs188055192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772389 | GGTCCCTGGTTTGGA[A/G]TAAGTTAGGGGCCCA | 23092 |
| rs188066101 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223913 | AACAACAGAGTTATC[A/C]GTATCTTCCACATGT | 23092 |
| rs188076425 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815804 | CTGCTCTTTTCTTCT[C/T]ATTTTTTTGAGACCA | 23092 |
| rs188082222 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775046 | CGATATAAACATTTG[C/T]GTGCAGTTTATATGT | 23092 |
| rs188087734 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813039 | GCCTCCTGGGTTCAC[A/G/T]CCATTCTCCTGCCTT | 23092 |
| rs188094156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186638 | AGCTCAGGATTGACA[C/T]CTCCATGTGAACATG | 23092 |
| rs188097366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940209 | TCCTTTCTTTGTTAA[A/G]ATAAGTGATTGAAAG | 23092 |
| rs188097685 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854166 | ACCTGTATACATTCA[G/T]GAAGCCACCACCACA | 23092 |
| rs188102763 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060945 | AAGCTCAAAGCAGTG[A/G]GTTCAAAAGGGAGAT | 23092 |
| rs188103660 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830271 | TCTAATAAAATAGCT[A/C]ATTACTATCAAGTAT | 23092 |
| rs188104058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142870993 | CTGAAAAATTCCTCT[A/G]TCAAGCCTGAGGTGA | 23092 |
| rs188105326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961365 | GGCATGGTGGTGTGC[A/G]CCTGCAGTTCCAGCT | 23092 |
| rs188106818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994142 | GTGTGAGGTGTGAAC[A/G]TAGTGCTATTGAAAT | 23092 |
| rs188116484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021197 | CTTGTATGTATTTTG[C/T]CAATGTCAGTATGAA | 23092 |
| rs188120396 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890092 | GGTGAGCCGAATTCG[C/T]GCCATTGTACTCCAG | 23092 |
| rs188133926 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883591 | GTATTCTGACATAGC[A/G]GAGCTTGTTAGGGCT | 23092 |
| rs188134004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150247 | ACTGTGGCTGAACCT[A/G]TTTTATGCCCAGACC | 23092 |
| rs188142540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812132 | CCAGTGCTTCCTCTT[C/T]GCTTCCTGTAGTATG | 23092 |
| rs188157239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922878 | GCCTTCCTGCTGGTT[A/G]GATTAGAGTGCTGGT | 23092 |
| rs188161711 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119208 | TAGTGTGGAGAAGCC[C/T]GACGGGGAAAAATGA | 23092 |
| rs188231998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032772 | CGTTGTTAATTATTA[A/G]TAATCTAATCAGCAG | 23092 |
| rs188234121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053669 | GAAGAGACAAAAGAA[A/G]TTGTCAGAGCTGATA | 23092 |
| rs188250361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015223 | AAAGAAGTAATTCCA[C/T]CCTACCCCACCCTTA | 23092 |
| rs188256388 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995546 | TGGAGAAATAGGAAC[A/G]CTTTTACACTGTTGG | 23092 |
| rs188259230 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221753 | TTCTTAAACTCCTGG[G/T]CTAAAGCAATTCACC | 23092 |
| rs188259395 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202964 | GTAAGACCTAAAGCC[A/G]TAAAAACTCTAGAAG | 23092 |
| rs188261116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914994 | GGCATGCTTTGTGTT[C/G]CAGCTCTCTGTCAGA | 23092 |
| rs188261368 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866208 | ATTCCCCTTAAGGCA[C/T]GGAATGTATACATAC | 23092 |
| rs188262889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980266 | AAGCATTTCGTTGTA[C/T]AGAACATATCACTAA | 23092 |
| rs188265267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933056 | AACTATAATTAAGCA[C/T]TGTTTAATCTTAATT | 23092 |
| rs188269453 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886505 | CAACTGTAGCAGCAA[C/T]AAAGGTTTATAATGG | 23092 |
| rs188289023 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057252 | CCTTGCAATGTTGTT[A/C]ATGTAAGATTTGTTT | 23092 |
| rs188290987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898991 | TCTGAAACCTGCAGT[G/T]AAAGGTGACTTCCTT | 23092 |
| rs188293762 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856691 | TTCTACTCTCAAGCA[A/C]TACAGTATAACAACG | 23092 |
| rs188311473 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938349 | GGTTGACAAACAATA[G/T]GGTCACTGTTGCAAC | 23092 |
| rs188319955 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892544 | AATGTATGTACAGCT[A/G]TGGGCATGATTCCTG | 23092 |
| rs188322806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116186 | ACTATTATAGAGTTA[C/T]TATATAGGTCAGATA | 23092 |
| rs188329611 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080358 | ATAGAAGTATAGACT[A/C]AATCCATTATAAAGA | 23092 |
| rs188331666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929703 | ACCCTTCACAGCCTC[C/T]GAGGTTGTCGAACTT | 23092 |
| rs188357005 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035673 | AGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23092 |
| rs188361733 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202583 | AAAAACTACTTTAAA[G/T]TTCATATGGAACCAA | 23092 |
| rs188364076 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082323 | TGTCACAAAAATATG[C/G]AGTTGTGTTTACTGT | 23092 |
| rs188374026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999144 | TTAGGAAATTAAGAT[A/G]CAGAGAGACGAAGAG | 23092 |
| rs188379736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120195 | GGCCAGCAAGTGAAC[A/C]ATCGAGTTTTATAGC | 23092 |
| rs188382465 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040347 | ATTAGTTCCATGTCT[A/T]CATAGGTCTTGTTGA | 23092 |
| rs188398530 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978028 | GACTCCTCTGACTTA[C/T]TTTCAGTGATCCGAC | 23092 |
| rs188402586 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003883 | AACCAGGTGACAAAA[A/T]AAAAACTTCATCCAG | 23092 |
| rs188405918 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791116 | ACAGAGTCTCGCTCT[G/T]TTGCCAGGCTGGAGT | 23092 |
| rs188413190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792747 | TGAGCAGCGTTGGAG[A/G]ATTTGAAAAAATCCT | 23092 |
| rs188426424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826634 | TGTTCTCTCTCACAG[A/G]ATTTTAGTGGTGGGA | 23092 |
| rs188431339 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154238 | TCAGTGTTTAACACA[G/T]TATGTCACACAGTAT | 23092 |
| rs188434476 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809199 | TGAATGGTTTTATTT[G/T]TGTGTTTTATCAGTC | 23092 |
| rs188436584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851482 | TATCCAGGCTTGAGA[C/T]TGTAATTTTAGTAGT | 23092 |
| rs188440958 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136309 | CTCAGCTGCAGAGCA[A/G]GCTGCTCTGTCCATG | 23092 |
| rs188444701 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894136 | GCTATTTGATTTGTT[C/T]TTGAAAATTATCTCC | 23092 |
| rs188445239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174369 | AATGTGAATAACTGG[A/T]GGTCATTTGTTTTTA | 23092 |
| rs188447646 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828431 | AAGCCCAACATGTAG[A/G]TGGTAAACTAGGATC | 23092 |
| rs188461377 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117186 | TTCTGAGCCATGTGA[A/G]GAGGAACTCAGACAG | 23092 |
| rs188465116 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983573 | CAAAGTCTATAGAAC[A/G]TAGATATAAAGGTAC | 23092 |
| rs188470626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977109 | ACAGAGCTGAGGGAA[A/G]GAGTACACTAAAGGA | 23092 |
| rs188472054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081447 | CTTTAAGACAATGAC[C/G]TATGTTTTCCATTGA | 23092 |
| rs188474393 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097648 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 23092 |
| rs188482685 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151677 | AGAAGTCAGTCTGGC[A/G]GGGTGCAGTGGCTCA | 23092 |
| rs188484479 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198842 | TAGATTCAGGGAGTA[C/T]ATGTACAGGTTTGTT | 23092 |
| rs188488632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180078 | TTTGAAGGCTCCTTT[C/T]CCCTTAAGAGTTCTT | 23092 |
| rs188504913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215869 | TTCATCAGTAGATGG[A/G]CACGTTGTTTCCTCT | 23092 |
| rs188507045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114401 | GACTTGGTAGAAAAC[A/G]TGCAGTGAGTGGCAG | 23092 |
| rs188525567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158113 | CCTTCTTCTTATTTG[C/T]TCTCAGACTGCTCCC | 23092 |
| rs188527233 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094751 | CTAAACTAATTCCAA[C/T]TGGCTAATTTAAAGA | 23092 |
| rs188532292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197306 | CACTATTTTTGAAAA[C/T]GATTGTAGCAATTTA | 23092 |
| rs188533569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054883 | AAGAATGCATGATTA[C/T]ATACCTCATGTATTT | 23092 |
| rs188535691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078165 | CAGCCAATCATGTTA[C/T]GCTAACTCAATAAAA | 23092 |
| rs188554129 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033304 | GGAAAACCAAAGGAG[G/T]AACATTTACTCAGAT | 23092 |
| rs188556416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157089 | CGTGGACAGATTAGA[A/G]ATGTCTAAATCAGCA | 23092 |
| rs188564981 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833505 | TTTTTAAGTTTTTTT[A/T]AAACTATTTTAAAGA | 23092 |
| rs188575542 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871263 | CCCTGGTTCAATGGG[G/T]GCCCCTGTGCAGAAG | 23092 |
| rs188577226 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209914 | ACACTGTAGTGTATA[G/T]CAAAGAGGTGGTGGT | 23092 |
| rs188593531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890913 | TTGGGCAGCTCTCTG[A/T]TGTGGGAGTCAATTC | 23092 |
| rs188595536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910042 | TTAGTATATAAAAAT[G/T]TTTTGGAACAAATCC | 23092 |
| rs188596348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873281 | CTTTTGTGCTTTGAA[A/G]TGGACTCAGGAACAA | 23092 |
| rs188609461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913016 | TCTAACATGGTATAC[A/G]AATGTAAGCTGCATG | 23092 |
| rs188614080 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951055 | TCCCTTCCCCTTCCC[C/T]TTCCCCCTCCCCTTC | 23092 |
| rs188619178 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096701 | TTTTTTTTTTTTAAT[A/C]TGTGAGTGTGTAGCA | 23092 |
| rs188622475 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173632 | TTTCCCATTTTTGCC[A/G]GTAGCAGCCTCAGAA | 23092 |
| rs188625004 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953072 | AGAGGATATAACTTA[C/T]AACACCTTGCACTAG | 23092 |
| rs188632810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828633 | ATAATTTAAGAAGAA[A/G]GGTTTTGCCCCCATG | 23092 |
| rs188633335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055881 | AATCTCAGAACGCTT[G/T]CAATAGGGAAACTAC | 23092 |
| rs188641555 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018245 | ATTCTAGATACTAAT[A/C]CCTTGTTAGATTTAG | 23092 |
| rs188642899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135876 | TTAAATATCTGGCTG[C/G]GGTCATTCTCACTGT | 23092 |
| rs188648237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005993 | CTCCCCAGTGGTACC[A/G]TAGGCTTCAAAACTA | 23092 |
| rs188652763 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988786 | GTTGTTCAGTTTCCC[C/T]GTAGTTGAGCGGTTT | 23092 |
| rs188660002 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869738 | AGGTAGATTCTAATT[C/T]TTAAAAAATTATGGT | 23092 |
| rs188662988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970082 | AGATACTGTTAGTCA[C/T]GTTAAGCAGATGAAC | 23092 |
| rs188666080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936932 | AAACTTTTAGAAGAA[C/T]GTGTGGAATCTAGGA | 23092 |
| rs188673614 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908147 | GTCCCACTCCCACTT[G/T]ATACCTGGAGAGCTG | 23092 |
| rs188673938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139577 | GGGTACCTCAATGTG[C/T]GTCCTGGCAGGCTGC | 23092 |
| rs188679679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100858 | CTCTTTGGGAGGCCA[A/G]TGCGGGAGGATCACT | 23092 |
| rs188689071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843478 | TACCATTCATTGAGT[A/G]CTTACTCCGTGCCAG | 23092 |
| rs188744236 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993113 | CAGCTTCCTGAGTAG[A/C]TGGGTTACAGGTGCC | 23092 |
| rs188747848 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212443 | CCAATACATAGACTC[A/G]GTTTCTTTGGCTCAC | 23092 |
| rs188760249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926615 | GCGTTACTCAGGAGG[A/G]GAAAGGAAATGGCCA | 23092 |
| rs188763385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946378 | ACAGCACCAGTTACA[C/T]TGACCCTCTTTCAGA | 23092 |
| rs188767917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175666 | GGGCATATGTGGGGT[A/G]TGGGAATTATTGTTT | 23092 |
| rs188773337 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155036 | GAGAAGGATCTTTCC[C/T]TTTAGATGGAGAATT | 23092 |
| rs188817721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214582 | TGCTGCACCTGATTC[C/T]GTGGGTCCTGGCTGC | 23092 |
| rs188819810 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953599 | AGTCCTGACCCTGGA[A/G]AACACTGCCTGTTAC | 23092 |
| rs188849006 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803974 | GTAGGTGCTTTCCAC[A/G]CACTGTCATAGTAAT | 23092 |
| rs188855538 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179027 | GGCACCTGCCACCAC[A/G]CCTGGCTAATTTTTA | 23092 |
| rs188861081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125761 | AGCTAACTTTTACTT[A/G]CAGCTTATTGTTTAC | 23092 |
| rs188861575 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781995 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCT | 23092 |
| rs188862833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783411 | AAACTGTATTCCCAC[A/G]GTGAGTCTTGGGTGC | 23092 |
| rs188864520 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822276 | ATGACTCAGACTCAC[A/G]GTTAATAAATGCAGC | 23092 |
| rs188866965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214765 | GAACAAGGCACAGAA[C/T]ATGAGGGTCTCTCCC | 23092 |
| rs188871925 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089941 | GACTAAAGCATAAGT[A/G]CCACTCCAGTTATTC | 23092 |
| rs188875985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107602 | TAGAACTTTGTCATT[A/T]AACACTTTGACTTCC | 23092 |
| rs188879166 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070031 | GTTTGGTGGAGTGCC[C/G]ATGGTAGCTTCTTGG | 23092 |
| rs188889642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153797 | CTTAACACACACGCT[C/T]ATGCATTTCCAAGTT | 23092 |
| rs188895923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218121 | ACACTCATGCCTTTG[G/T]GTCTGCGTGTTATCT | 23092 |
| rs188898363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025533 | GCCTTAAGGCAGAAG[A/G]GAATTGAGGCCACTG | 23092 |
| rs188898788 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048267 | TTTTTGTTGTCTTAT[A/G]ACTATTTTATTGAGA | 23092 |
| rs188899736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193135 | TGCTCCCCGGGACAG[C/G]AATCATCCCTTTGCC | 23092 |
| rs188904927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985711 | TCACCCTGTGTCCAA[A/G]TGTTCTCATTGTTCA | 23092 |
| rs188906342 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116625 | CAAGGGTTGGCTACT[G/T]CTATTCCCATCATAA | 23092 |
| rs188911213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966227 | CTGTAGGAGAGGGCA[C/T]GCACACCTACACAGA | 23092 |
| rs188911434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010710 | TCAGGGAATGCTTGG[C/G]TGTTCCAGGAAGGGG | 23092 |
| rs188916219 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812814 | AGTCTTTGGAGTTGA[C/G]GGCATAAGCCACCGT | 23092 |
| rs188917123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990751 | CCTGTTTGCCTGAGT[A/G]TCACCAGTGGAGGCT | 23092 |
| rs188918221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991733 | GTTTATCTCCTAGGA[A/G]CAATAGGCTACACCA | 23092 |
| rs188928177 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777044 | CCTTTTCATGTGTTT[G/T]TTGGCCATTGGTGCG | 23092 |
| rs188929027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853956 | AGCAGGCCAAGAACA[A/G]CAATGTGGCAGGGTG | 23092 |
| rs188930289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806730 | CCCCCCCACTACTTA[A/G]ACATCTAACTCTGTG | 23092 |
| rs188938841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043421 | CCATTGTATGGATGT[A/C]CTGCACTTTGTCGAA | 23092 |
| rs188939959 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889277 | GGAGGAGAAAAATGA[A/T]AAAATTAGACGAGGT | 23092 |
| rs188942069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080864 | CTAGTGTGGTGTTGG[A/G]GAGGCTGAAGCAGTA | 23092 |
| rs188952126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956501 | AGGATTGCTTGAACC[C/G]AGGAGTTCGAGGCTG | 23092 |
| rs188955774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023302 | ACATCATTACCATTG[C/T]TCTGTTTCCTATTGT | 23092 |
| rs188958013 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006251 | GACACCTGAGCACAC[A/T]TCTAGCTTTCCTTTT | 23092 |
| rs188959074 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846175 | GACTCATGTTGAGTT[A/G]TATGCCAGACGCTGG | 23092 |
| rs188963142 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882405 | TAGATACACACAGTT[A/C/T]ATTTGTTTAAAAAAT | 23092 |
| rs188971079 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989108 | TTAAATTCTCCCATT[A/G]TTATTGTGTGGGAGT | 23092 |
| rs188986712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779099 | ATGGGGCTTTGCCCA[C/T]ATCTAAGAGTCTATT | 23092 |
| rs189002452 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799042 | CAATCTGGTATACCT[C/T]GAAGAGATAATGTGT | 23092 |
| rs189018628 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818939 | GTATATCTGGGAAGG[G/T]TGCTCACCCAGCTTC | 23092 |
| rs189030713 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835763 | GTTAGCACATGATAC[A/G]TAATAAAAACCCAAT | 23092 |
| rs189060138 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901847 | TTTATTTTAGACTTT[C/G]AAGCCAGTGTTGGGA | 23092 |
| rs189092136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930719 | ACACCCCTACCCCAT[A/G]CCCCTTGTATCCTCA | 23092 |
| rs189094719 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112861 | TATCTGTTCATCCAT[C/T]AGTAGACATTTGGGT | 23092 |
| rs189100599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075847 | GGGACTACAGGAGCA[C/T]GCCACCAGGCCCAGC | 23092 |
| rs189115688 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103396 | TGTGGCAATTCTTCA[A/G]GGATCCAGAGCTAGA | 23092 |
| rs189122010 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064412 | CTCTTTTTTTTTTTT[G/T]TTCTCCTGGAAGATT | 23092 |
| rs189122652 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785808 | CCAAATGTAGAAAGC[A/G]TGTTTTCTACCATCT | 23092 |
| rs189125327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111767 | TAATAATTATTAGAC[C/T]TCGTAAATATTTTTT | 23092 |
| rs189129120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823501 | GGCTCTTGGGACTGT[G/T]TGACGTTATACACCA | 23092 |
| rs189129347 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084999 | ACAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 23092 |
| rs189138982 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863117 | TGAGGTTTTTTTTTT[C/T]TTTTTCTTTTTGAGA | 23092 |
| rs189139675 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163716 | TCGGTCTCCCAAAGT[G/T]CTGGGATTACAGGCA | 23092 |
| rs189142739 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198015 | AGGCAGTCATAGTTT[C/G/T]TTGCTTACAGATTTT | 23092 |
| rs189149654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202768 | GGCCTCAGAAATGAC[A/G]CCACACATCTACAAC | 23092 |
| rs189153543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927935 | GGGCTCTATTTCTTA[A/G]CCTTATTGGCCATTT | 23092 |
| rs189154014 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184238 | GTCCCTTCCTGCCCA[G/T]TAGGGGGTAGAGAAT | 23092 |
| rs189157931 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005789 | CAGTTTTTATTCACC[A/C]GCAAGAACGCTTCCG | 23092 |
| rs189161333 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045978 | CTCTACTAAAAATAC[A/C]AAAAAATTAGTCAGG | 23092 |
| rs189166510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900545 | CCTGCCCTCTGAGTT[G/T]AGGTCCAGTGCTATA | 23092 |
| rs189171971 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146433 | TTATAGATTGTTAAC[C/T]AGGAATCCAAGATCA | 23092 |
| rs189173126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969329 | TTTCAGGAAGGCTGG[C/T]CATTTTGTGATGAGA | 23092 |
| rs189173900 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107988 | TAAATATAACAGAAG[A/G]GTTTGTGTGTTCACT | 23092 |
| rs189174774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879756 | TTATAATAGATAGCT[G/T]TGTGCTTAGACAATT | 23092 |
| rs189176915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899653 | GTGGGCTTCATCCTG[C/T]CCCCTGAGGAGTGGA | 23092 |
| rs189180833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126484 | CCTTGGAAGCTGAAC[C/T]AAATAGTACTTTGAT | 23092 |
| rs189184400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008976 | TATGAAGGCTTTCCT[C/T]GCCCTCCTTTGATTT | 23092 |
| rs189185625 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:142919440 | TAAATTTCTGTTGAT[A/T]AAGCCAGCCAGTTTG | 23092 |
| rs189191140 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226219 | GGGTGCAGTGGCTCA[C/T]GCCTATAATCCCAGC | 23092 |
| rs189195190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939775 | CAGGTTTCCTCACCT[A/G]CAAATTGTGATAATA | 23092 |
| rs189201318 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018697 | AGGTTTTTTGTGTAG[C/T]TGTTTTTGTCCCAAT | 23092 |
| rs189203153 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972476 | TTTGTTTTGTTTTTT[A/T]AATACAGGCTTAAAT | 23092 |
| rs189205885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142959440 | TGTGCTTTCACCTGG[A/G]CTTGGGGCCCTTTTC | 23092 |
| rs189212744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985016 | CAGCTCTATGTGTGT[C/T]ACTGCTCCTGAAGAC | 23092 |
| rs189228974 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824216 | GTCCTGGGATGTTCT[A/T]GCAATCCAGGTTCTT | 23092 |
| rs189237656 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863886 | TGAGGCTCAAGCCAG[C/G]ATCAACCCTCCCAGC | 23092 |
| rs189296408 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906448 | CCACATTTAATAGTT[A/G]CCATTCAGTGTACTT | 23092 |
| rs189296754 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163984 | ATTTGCATGTGTTGC[A/G]TTTTTGAAGTCCTCC | 23092 |
| rs189299171 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221161 | TTCCTTCCTGCTATT[A/G]ACTACTGTGCAGACT | 23092 |
| rs189304613 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194689 | AGAGAATATAAAAAT[A/G]ATTTTCCTTCAATTT | 23092 |
| rs189314277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945786 | AACACAGTACAATGA[C/T]CAGACCTGGAAATTA | 23092 |
| rs189328035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126934 | ACATAAAGTAGGCAA[A/T]AACTTAAGGTTATGG | 23092 |
| rs189333467 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823087 | ATAGGGCAAGGGGCA[A/T]CACTATTCCCATTTT | 23092 |
| rs189344490 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843717 | ATAGTAGAAAAAGCA[A/T]TGAATTATAAGTCAG | 23092 |
| rs189358475 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090537 | GAAGGTGCAGGTGGC[A/G]GGGGATCAAAGAAAC | 23092 |
| rs189364351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056557 | TTCCATTATGTCTTC[C/T]ATTTACAGCTTCTGA | 23092 |
| rs189364679 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036433 | GAGAATCCTGTCACC[A/G]CTTGCTCATTTCCCC | 23092 |
| rs189366436 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862805 | ACTGTAAGTTTACGA[C/T]GATAAATTTTCAGAT | 23092 |
| rs189369338 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094378 | CTGAGAGCTCAGGTT[A/G]TTCCTCGCACTGGGT | 23092 |
| rs189371780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049876 | ATGCTGTGGTTCTTC[C/T]CTTATGACTCTCATG | 23092 |
| rs189373406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130937 | TGGACATTTTGCAGT[A/G]TGCTTCCTTGCACAT | 23092 |
| rs189376390 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181206 | ACAGCACTCTCCTGC[A/G]TAAGAGTCTTTGATG | 23092 |
| rs189382467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207079 | TGACAGCACATCCCT[A/G]GGTTTCGGTGCTCCT | 23092 |
| rs189384530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159269 | CCCGAGGTTGCAAAA[A/G]CCCTGTTGAAGAAAT | 23092 |
| rs189384637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199880 | TTTTGAAAGTCCTAC[A/G]CTAAGCTACAAATCC | 23092 |
| rs189390465 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224735 | CTGCTGCTTTCCCTT[C/G]TCCTAAACATTTTAA | 23092 |
| rs189392028 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168596 | AAAGCCAACAAAATA[A/G]GTTCAAAAATAAGCT | 23092 |
| rs189397495 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804555 | GGAGTGCAATGGTGT[A/G]ATCTCGGCCCACTGC | 23092 |
| rs189400252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141909 | TCCTGTGGATCAGTG[C/G]AATCCCAGGCCACCC | 23092 |
| rs189417579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143162 | AGAGTCCCATGCATG[A/G]GGGGAAACCTCCCGC | 23092 |
| rs189419782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122533 | CAAGTTTAGTTTAAA[G/T]ATGTTAATTGACTTT | 23092 |
| rs189426325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101958 | TCCTTAGGGGCTGTG[C/G]TGGCGCTGATAGAAC | 23092 |
| rs189427281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909015 | GATAGCCCTAGCTTT[A/G]ATTTTTTTCTTTTTT | 23092 |
| rs189429132 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843974 | GATAACTGTCTCCTT[C/T]CATTGTTGTGGGGAC | 23092 |
| rs189430431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798553 | CAAATGGAGTATTGT[A/G]TAGCATTTTAGGAAG | 23092 |
| rs189431511 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880473 | CAGTGAGCCGAGATC[A/G]CGCCACTGACTGCAG | 23092 |
| rs189434506 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834803 | ACTGTATCACAGAAT[A/C]CAGAGAGTGGAGAAA | 23092 |
| rs189447139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949708 | GGGCAGAGTGGGAGG[A/G]AGGTAGCTGGAATGT | 23092 |
| rs189447522 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987743 | GCCTTTTCTGTATCT[A/G]TTGAGATAATCATGT | 23092 |
| rs189452895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064146 | TGACAATTGGCTGGA[A/G]CTGAGTAGAAGCCAC | 23092 |
| rs189455108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995722 | GCACACATATGTTTA[C/T]TGAGGCACTATTCAC | 23092 |
| rs189455212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920814 | ACTAAGGTATAAACA[C/G]CAGGATGTTGAGTGT | 23092 |
| rs189459253 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022968 | AGTTCTTTGTGGCTG[A/T]GGGGCCATCCCATAT | 23092 |
| rs189466953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875014 | GCATCTGTATGTGCC[A/G]AGGAATTAAAATCCA | 23092 |
| rs189480457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819332 | GGAGTCTGGGCTGTG[A/G]GTGGGTGGGCATGTT | 23092 |
| rs189493347 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000677 | TGGGGCACATATACA[C/T]CATGGAATACTATGC | 23092 |
| rs189498152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789420 | GATGTCTTCGTTTTA[A/G]TCTATCTAGTCACAA | 23092 |
| rs189500843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837038 | AATCTCTCGCAGAAC[A/G]CATTTGGAAACCAAA | 23092 |
| rs189507667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966016 | TTTTCCCCTTGCATT[A/T]TGGGCAGTTTGGTTT | 23092 |
| rs189510200 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876130 | CATATCCCTAAGATA[G/T]GAGGAATGAAGTCCC | 23092 |
| rs189510366 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859793 | CTCTGTCCTAGGTTA[C/T]CATGATCAGTGTCAG | 23092 |
| rs189522582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945349 | ATTCTATTCTAAAGG[A/G]CAGTCTCTGTTCTGC | 23092 |
| rs189526601 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895652 | AACTTTTGGGGTGGA[A/T]TTTTTTAGGCATGTA | 23092 |
| rs189528302 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915454 | ACCTCTGCCTCCCGG[A/G]TTCAAGTGATTCTCT | 23092 |
| rs189538075 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934617 | GTTAAATCTGTCCCC[A/G]TGGGAGCTTTGGATT | 23092 |
| rs189548524 | snp | A/G | 6.68003e-05 | 0.0057789 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207506 | GACCAATCTGTTCCC[A/G]TTTATCCAAAGCTGG | 23092 |
| rs189566113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018443 | CAAAGATGTGTACCT[A/T]TGTTTTCTTTTATTG | 23092 |
| rs189571636 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813838 | GGAATTTTAGGGGCC[G/T]CAATTCAGCCCTTGA | 23092 |
| rs189572096 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964184 | CTTTTACCCTGAAGG[A/T]TATAACAGTTATGTT | 23092 |
| rs189577147 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999748 | GGACATAGAAAGTGA[C/T]AGCCCTACAAAAACA | 23092 |
| rs189584856 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984237 | AATCGCCTGTATATA[G/T]CCACTTATGTCTCAT | 23092 |
| rs189586047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924563 | GCACATAATAAACAC[C/T]CAGTAAATCTACCTG | 23092 |
| rs189586308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210720 | CCTCCCTGTAGTGCC[A/G]TATGATGGCGAATGG | 23092 |
| rs189592386 | snp | A/G | 0.000333061 | 0.0129004 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143147369 | TGGTCAAACCCACCC[A/G]GCCCAACTCACTGTA | 23092 |
| rs189594555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879253 | ACAGTTGACATGTAC[A/G]ACACTGCCTCCCCAA | 23092 |
| rs189594926 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965555 | CCCTCAGCTCCTATC[C/T]CTGTATGGCCTGGTT | 23092 |
| rs189618850 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086801 | GGGTCTTATTACTAC[A/G]GAACTAACTTTAGTT | 23092 |
| rs189623084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055656 | TTCTAACAACAAGCC[A/G]CTGGGAAGATCAAGA | 23092 |
| rs189625206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034437 | ATAAGTGAAGTACTG[A/G]TGCTACAACATGGCT | 23092 |
| rs189626013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108975 | GTCCCTTAACCTTTG[A/G]TTTAGCTCCTTTTGT | 23092 |
| rs189631663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017563 | CTTTTAGTTCTTTTT[C/T]CTAAAATGTGTGTCT | 23092 |
| rs189632828 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071242 | ACTACGAAGCTGTAG[C/T]AACCAAAGCAGCATG | 23092 |
| rs189642163 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997734 | ATAAATGCCCTTTTC[A/C]CACTCCATTTAGTGC | 23092 |
| rs189651091 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891668 | TGTTCCAAGTTTCTT[C/T]TGTAGGAATGTTGAC | 23092 |
| rs189656977 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183682 | GGGGCCTCCTCGGAC[A/G]CCACCCCTACCTCTG | 23092 |
| rs189668047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912071 | TAGTTTAGATAAAAA[A/G]GATTGACAGAGGCAG | 23092 |
| rs189674319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929180 | TTGACCTCATGGTCC[A/G]CCCACCTCGGCCTCC | 23092 |
| rs189683909 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778355 | AGCATCAAAGAGTAT[A/T]GACGTATACAGTGTA | 23092 |
| rs189688522 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121569 | TAAATTTTAGGGATA[C/T]TAAACTTTCTTCATT | 23092 |
| rs189707196 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223400 | GCACACCCTAGTAAC[A/C]TCTTGAGATTAAATT | 23092 |
| rs189719084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818122 | ACAGCTTGGGTATTG[A/G]CAGGCTTCCTTGGTT | 23092 |
| rs189719172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084671 | TCCATGCCAAAGGCT[C/T]GCTGCTTTGGGAATA | 23092 |
| rs189721355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016196 | AAAAATTAGGCTATA[C/G]AACAACATACATAAT | 23092 |
| rs189730509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042920 | GAGGTACTCTAGCAA[C/T]GAGTATCTGGGTTTT | 23092 |
| rs189733323 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858044 | GAGAGAGAAGGAATG[A/G]GAGAGAGAGAGAGAA | 23092 |
| rs189774622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773226 | GTTTATTATATCTAT[A/G]AACAGAAGTGTTTTC | 23092 |
| rs189799303 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795454 | TCCTTTTTCTCTGTT[C/T]TGGGCAACTCTTCAT | 23092 |
| rs189813053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177507 | GTAGCAGACACGTAC[A/G]TGTATTTGATATGCA | 23092 |
| rs189814180 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815149 | GGGATTACAGACCAG[C/T]GCTGCTACACCTGGC | 23092 |
| rs189826628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855838 | AATGCCATGAAGGCA[C/G]AGCCTGTCTACTTTT | 23092 |
| rs189831760 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226048 | GTGGAAGACCATGGC[A/C]CAGGATCCCTGAGCT | 23092 |
| rs189834599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832277 | TACTTGGAGATAGGG[A/C]CTATAAAGAGGTAAT | 23092 |
| rs189836355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196365 | CGCGGTAGTCATGTT[C/T]TATAAAGTCACTGCA | 23092 |
| rs189836888 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872342 | GTACACCCCCCCACC[A/T]CCCATATCTTATTAA | 23092 |
| rs189849907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862018 | TGCCGTCTGTGACTT[C/T]CCGAATTCACAACTG | 23092 |
| rs189850450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028107 | CTACTCACTGATGCT[A/G]TAATCTTACAGAAAT | 23092 |
| rs189851149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156336 | TCCTTCTCTGCATTA[A/G]GGATCTGGAAAGCCA | 23092 |
| rs189854515 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011978 | CAGCTCTGGCTGAGT[G/T]AGTCAGAAAAACCTA | 23092 |
| rs189855465 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794687 | GAACAGGGATGTCAG[A/G]CAGATAGGAGGGAGA | 23092 |
| rs189856846 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118946 | AAAGTATAATAATAA[A/T]AAAAAAAAAAGAAAG | 23092 |
| rs189859711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830889 | TGCCTGCTCTCAAAT[C/T]TCCATAGCTACGTGA | 23092 |
| rs189868458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082083 | ATCTGTTGCTGGGGA[C/T]GTTTGAGAGTTTGGA | 23092 |
| rs189868670 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992411 | AGTGCAGCAGTGATT[A/T]TTTATTTATTTATTT | 23092 |
| rs189872511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099937 | TTTTAAATATTGTTG[A/G]AATTAAAAACATAGC | 23092 |
| rs189873165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975846 | GTTGAGGTGTACCAT[A/G]CATGTATTTATCTTA | 23092 |
| rs189899384 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117533 | AATAATGAAAGGTGT[A/T]ACTCTTCCCACCCAA | 23092 |
| rs189903529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081624 | GTTTATAAAATGGGA[A/G]GAATAATAGGATCCA | 23092 |
| rs189909175 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145868 | GTGTATGTATTTAAC[G/T]TGAGGCTTACTCTAG | 23092 |
| rs189911198 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789160 | CTTGGGAGCATTGGA[A/G]GAGTTAAATGGGGTA | 23092 |
| rs189917736 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096014 | CTCTACCAACATTCA[A/T]CAAGTGGTAATTTTT | 23092 |
| rs189919534 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038269 | TTTTCCATAAGGACT[A/G]TGAGGCATTAAGTAG | 23092 |
| rs189923741 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825239 | CACAGTACATGCTCT[A/G]TGTTAGTAACAGTAA | 23092 |
| rs189926398 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137071 | ACCTTAAAGCAACTC[A/T]CTTCTTTCCCTGGCT | 23092 |
| rs189940862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859222 | AGGCCAATTAGGAGT[C/T]CAGGCCAGAGATGAT | 23092 |
| rs189941003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001217 | AGGTCTGAGGGAACT[A/G]TCTGAGCTGATGTTT | 23092 |
| rs189952424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792503 | CAGATGCCCTGTTTG[A/G]CGACATCTAAGCACT | 23092 |
| rs189966064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895099 | CACCAAAATAGTATA[C/T]GGACCTCAATTTAAA | 23092 |
| rs189966968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811968 | CCTAATCATAGCACT[C/T]GAAGAACTCCTGGTC | 23092 |
| rs189976384 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853211 | ATTTTTTGAGACAGG[G/T]TCTTCTTTTGTCGCC | 23092 |
| rs189976554 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973718 | GGTCTGTTACATACC[C/T]TAAGACCCAGGACAT | 23092 |
| rs189982365 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828267 | CTTTCTTATGGAAAA[G/T]ATTTTGAGTGCACTG | 23092 |
| rs189984738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934208 | ATTTGTTCTCTGTCT[A/G]CGTATAATTGGTCTT | 23092 |
| rs189994789 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916097 | GGGATGGTTATATTT[A/C]ATCGCATAAGGGTTT | 23092 |
| rs189996463 | snp | A/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868738 | GCAGAGGGTGTTTGA[A/G]TAGAGAGAGTTTTGT | 23092 |
| rs189999292 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093603 | CTTTCTCTCTGTCTT[C/T]GACTCCATCTTTGTC | 23092 |
| rs190000779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888252 | AGCACTGGCTGTGCA[C/G]CCCTTTCCCTTCACC | 23092 |
| rs190001385 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052677 | GAGAGCAGTAGATAC[C/T]AGCTGGATTTGTGCC | 23092 |
| rs190002642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935045 | AGAATTGTCTTCCTA[C/T]AATAAGCATTATGGA | 23092 |
| rs190004889 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907627 | CATTATGAATTATGG[G/T]TTGTGGTTTTTCCAG | 23092 |
| rs190010722 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955771 | AAATAGACAAATGAT[C/T]GGTTCCAGATGTTAG | 23092 |
| rs190030137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013789 | TAATTTTAATTTTTT[C/T]CTCTTTTCTATTTAT | 23092 |
| rs190042701 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978966 | TAAAGGAAAAAGGAG[A/G]CGAAACTGTTTAAAA | 23092 |
| rs190045746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954184 | CATCAAGATCTGTTT[A/G]TCTCATTCTTTCCAT | 23092 |
| rs190065292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172866 | GGGAATATAAATACC[A/C]GAAGGGCAGATACCC | 23092 |
| rs190067030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217264 | TTCCAGGGGCCCCTA[C/T]TGTGACTCTGGAGTG | 23092 |
| rs190095512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152775 | AAAGAAGCCTGTTGT[A/G]GCCTCCTTAAAGATG | 23092 |
| rs190096910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200263 | CCTTTCTGGAAAGCT[A/G]TTTGGCACGGTATAT | 23092 |
| rs190097990 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025005 | GGTTTTTTTGGAAGA[A/C]TAAATGAGATTAGGA | 23092 |
| rs190098691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115882 | CCTTAGCTTTATTGT[C/T]CAAATTTGCAAATTG | 23092 |
| rs190103100 | snp | C/T | 9.91736e-05 | 0.00704109 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143133994 | GTGCCCGATATGCCT[C/T]TCACCAATGCCCAGC | 23092 |
| rs190105301 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181678 | ACAAATGAATTACAC[C/T]GGAATAGATTTCTGG | 23092 |
| rs190105578 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214499 | CATTGTATCCATCTT[C/T]GAAAAAGGCCCTGAT | 23092 |
| rs190109692 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786489 | GTGTTTTTAGAGATA[A/G]GATCTTGCTGTGTTG | 23092 |
| rs190110350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871924 | GGTGTAGAGCAGAGC[A/G]CTTTGGACAAACCGC | 23092 |
| rs190111973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008163 | TGTGTTGAATATTGT[A/G]TATCTATGATTCCAT | 23092 |
| rs190115980 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990186 | CTAAACTTCTCTTCT[C/T]GCTTCATTTCATTCA | 23092 |
| rs190124714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910890 | GAACAGAGCTCTCCT[A/G]GGAGCTAGAGGTAGA | 23092 |
| rs190126175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971705 | AGGTAGACACAATTA[A/T]CCCTGTTTTGCATTT | 23092 |
| rs190133523 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199491 | GGGATATTTTCCAAG[A/G]AAGAAGAATTCAATG | 23092 |
| rs190134513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823996 | GATGAGTACTGTAAA[A/C]GTTTGGGGACGACTT | 23092 |
| rs190137728 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951431 | TAAAAAGAGAAAAGA[A/G]GAAGCACCAATATTT | 23092 |
| rs190140532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805018 | TTGAAGCATGTGTCA[C/T]GAGCTTATTCCTTTT | 23092 |
| rs190143941 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098037 | CTTCTCAGAATTCCA[C/T]ACAGTTTTTACTATA | 23092 |
| rs190144994 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197159 | TTTCTGCTTTTACAA[A/G]TAATTTGCTCTACAC | 23092 |
| rs190147089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929505 | TCCAGAATAAAGATA[A/G]TTCACCCTTTTTATC | 23092 |
| rs190149067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178633 | TCATTTCTGTCGTTG[C/T]ACTTAACAACAGCTG | 23092 |
| rs190150878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844580 | AGAATAAGAACTCTT[C/T]TAGGCTGGGCGTAGT | 23092 |
| rs190152330 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159027 | ACAAGAGATAGTAGA[A/G]TAAGCCAGGGCTAGC | 23092 |
| rs190156262 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952805 | ACCTCCGCCTCCCGG[A/G]TTCAAGCAATTCTCT | 23092 |
| rs190156337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122178 | CTAAGAATTATCCAG[C/T]GGCTTCCCATTTCAT | 23092 |
| rs190157486 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163358 | CCTAGTTCGTTTTCT[A/G]GATCTGCCTTGAAGT | 23092 |
| rs190161586 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808028 | ATCACGAGGTCAGGA[A/G]ATCGAAACCATCCTG | 23092 |
| rs190162963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863386 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 23092 |
| rs190177961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143058341 | AAGAATAAAGGAATT[A/G]TTTTTGGCAAATACT | 23092 |
| rs190190000 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019032 | TTCTGCCTAGAGATC[A/G]TGTGTGCTCCTGGTC | 23092 |
| rs190203960 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875814 | GGTACCATCATAGCT[C/G]ACTACAGCTTCAAAC | 23092 |
| rs190224316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915228 | ATAAGCAAAGAGCGA[A/G]TGTGTCACATTCAGC | 23092 |
| rs190243034 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074534 | AGAAGAGTAATACTT[A/C]ATGACACATGAACAT | 23092 |
| rs190254844 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070925 | GCAGAAAAAAAAACA[A/C]CAAAAAAACAGGGAC | 23092 |
| rs190256848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804251 | GAGACCCAATATTAT[A/G]TACACACACATATAT | 23092 |
| rs190266493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031823 | CCTCTTGGGTTCAAG[C/T]GATTCAAGCCTCCTC | 23092 |
| rs190273575 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027788 | GCAATTGACTAAATT[A/G]AGTCATTTTTGTTTG | 23092 |
| rs190278790 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970812 | TTTCTGTAAGATGTG[C/G]GTGGACAAGGAAGAG | 23092 |
| rs190282893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994753 | TTGGCTGCTGTTTAC[A/T]GAGCATTTACTCTGT | 23092 |
| rs190283250 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991980 | CTGAGCCTACATCTA[C/T]ACTAGTTGCTACCAA | 23092 |
| rs190300805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148299 | TGTCGGTAACCTTTT[A/C]CTGCTCCTCCACATG | 23092 |
| rs190308087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906941 | CTAGTATTGGTTGAA[A/G]TCCTTTGCAGGCTGA | 23092 |
| rs190314614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925024 | CAGACAACAGAAGTT[G/T]CAAACTGGTGGTCCA | 23092 |
| rs190322016 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109247 | TCCCAGTAGAGGTCT[A/C/T]CAGCACAATGACCAA | 23092 |
| rs190328392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128029 | GGTTCTTGCTTGTAC[C/T]CTTTTTGTTCCTCTC | 23092 |
| rs190334374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912353 | ATAAAATTATAGACT[A/G]TGCAAACTAATCAAT | 23092 |
| rs190336542 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091059 | GGTCAGCAATAGAGC[A/G]AGTAAAGAAAAAAGA | 23092 |
| rs190367899 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891065 | AGCTTTGAGGTGTGT[C/G]GGGTGGTTGGGAGTA | 23092 |
| rs190371404 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176903 | TTGCAAAGAGAATTA[C/T]GTATTGCAAGGAGCC | 23092 |
| rs190372656 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180729 | CACGGAGCATTCACC[C/G]CCATGATCCAGTCTC | 23092 |
| rs190378796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928552 | GCTCTCTGGGGGCTG[C/T]GGTGCCATCACATTT | 23092 |
| rs190382803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216485 | GCCTCATGCCTTCTT[C/T]ATGTTCTCAAGCAAG | 23092 |
| rs190409095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850131 | TCTTCAGAGCTCTGC[C/T]TACCTCTCCTGCTCT | 23092 |
| rs190411611 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142468 | AATGTATAGAGTCTA[C/T]CATCACCCAAACTCC | 23092 |
| rs190414144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217016 | GTCTTTTTCCTTGTT[C/T]CATTTCTTGTTAGTT | 23092 |
| rs190422160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885945 | GTTTCAAGAAAATAC[A/G]TTCTTAAATTTGCGC | 23092 |
| rs190440721 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924014 | CTACAGGCGCCTGCC[A/G]CCGCACCTGGCTAAT | 23092 |
| rs190451432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781905 | TTTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 23092 |
| rs190463753 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801961 | TGCGGGTCAGATTCC[A/G]TAACCTCGTGGAGAG | 23092 |
| rs190471900 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151232 | AGATACCACTACACA[C/T]CTCTGAGAATGGCCA | 23092 |
| rs190473346 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188373 | GGCCCCAACCCTGCC[A/G]TAGTCATTCAATTTC | 23092 |
| rs190477171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866835 | GTGGTCGGTGGGCAC[A/G]TCATCCGCCTGGGGG | 23092 |
| rs190479192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820567 | ACAAGTGTTTGTGAG[C/T]GGCTACGATGGCCTC | 23092 |
| rs190487367 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887380 | TGTTAAATACTCATG[A/C]AATATCTGTCCTACT | 23092 |
| rs190493707 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860567 | TGAGCTGGGTTTCTA[C/T]AAAACAAAGATGTGT | 23092 |
| rs190495130 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090443 | GTCTTTAACTTCTAC[A/G]ATAGCTATCTCAGTC | 23092 |
| rs190499982 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839333 | GTGTTAGTTATAATA[A/G]CCCCATTTAATTGTT | 23092 |
| rs190502789 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049089 | CTTTTATATATCACC[A/G]TGTAATCATTCTTTT | 23092 |
| rs190518137 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980985 | GTGTCACACTTGGTG[A/T]TTATTTTCATTTCCT | 23092 |
| rs190527236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011524 | CATGGATAAGTAAAC[A/G]AATTGCAAGCAACAT | 23092 |
| rs190550711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072460 | CTGCACACTAATGTT[G/T]CTTGCACCACTATTC | 23092 |
| rs190558445 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051259 | GCCCTTGGGACTGAT[C/G]CAAGTGTGACATTTC | 23092 |
| rs190558909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028364 | TATAGTTTATTAATT[C/T]ATTTTATAAACTGTA | 23092 |
| rs190565752 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012294 | AAAGACCTTCTTGGG[C/T]GACTCCTTCAGTTTA | 23092 |
| rs190577367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808367 | GAGGTGGGGAAATCC[C/T]AATCATCTAATTGGT | 23092 |
| rs190591858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863900 | GGATCAACCCTCCCA[G/T]CCCCACTGCCTCCTA | 23092 |
| rs190609415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902674 | TCTTTGTCTCTAGGT[G/T]ATCTTGTGTCCATGT | 23092 |
| rs190615680 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844925 | TTGCAGGCTATTCCT[C/T]CCCTGCTCTCTGATG | 23092 |
| rs190617081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196075 | TTAAGATAGGCTTGA[A/C]CGTGTATTAAAAAGT | 23092 |
| rs190622244 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863652 | TCTTCTCTGTCAGGG[C/T]CTTGAGTGGGAGTCC | 23092 |
| rs190629380 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942313 | TCAGAATAATGCTTT[C/T]ACATGTATAAAATAA | 23092 |
| rs190638254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882141 | GTAGAGAGTGGGTCT[A/G]CAGCTAGACTGTCTG | 23092 |
| rs190640840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825730 | CAAGTAGTTAAGAGC[C/T]GATATTCCGAAGCAA | 23092 |
| rs190642605 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901435 | ATTTTCTTTGATTTG[A/T]CTTTGCCTGTTAGAC | 23092 |
| rs190654827 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865383 | AAAAGCCAATACAGC[A/G]CTTTGGAAATACATA | 23092 |
| rs190663324 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941915 | TAGACATTCTTCTTT[C/T]AACATTGAGCAAATA | 23092 |
| rs190671707 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962984 | GTAGGCTCCAGTGTC[C/T]GTTGTTCCCCTCTGC | 23092 |
| rs190674445 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905611 | CATACACACTTTTTT[C/G]TGAGTCATTTGAGAA | 23092 |
| rs190681687 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204132 | ATACCAATTCAAACA[C/T]AGTGGTAATAAATGT | 23092 |
| rs190713897 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044168 | ACAAAAGTGTCAAGA[A/G]GACAATTCAGAATAG | 23092 |
| rs190714357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167823 | TGCAAAGAGAAACTG[A/C]CAAGAGATAGTGGAA | 23092 |
| rs190723003 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007434 | TTTGTAGAATTCCTG[G/T]TATGCTTAAATTGGG | 23092 |
| rs190729996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098316 | GCATACAATTCCGCA[A/G]TGTCATTTTAACAAT | 23092 |
| rs190740083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059800 | GTTTTGATCATTTAA[G/T]TATCAAGAAATCTAC | 23092 |
| rs190740249 | snp | C/G/T | 0.0422008 | 0.138995 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081902 | GTAGTCCCAGCTACT[C/G/T]GGGAGGCTGAGGCAG | 23092 |
| rs190742539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975227 | AAAAGCTGCTCACCC[C/T]TCCTAGGCCTGTGGT | 23092 |
| rs190743595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971337 | ATGAAATTGCAGGAG[A/G]AGGAAAGCATCTATA | 23092 |
| rs190746057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190367 | ATGAATAGTGCTGCA[C/T]GGGGCAGGGTGCTTG | 23092 |
| rs190754556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208154 | GCTTTTGTGACTTCC[C/G]CACTTAAGTTTTTTG | 23092 |
| rs190756723 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038791 | AACTCCAACTCCCTG[A/G]TTCAAGGGATTCTTC | 23092 |
| rs190758917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019850 | TGACAGATTGAGGCA[G/T]AGAGGGCTCAGTCTC | 23092 |
| rs190767114 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001969 | GACAGCTGTTTGTGG[C/T]AAGGGAAGAAGTCAC | 23092 |
| rs190768684 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132165 | AGACAGCTGTGTTTC[A/G]GAGTGAGACTGATTT | 23092 |
| rs190777023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088902 | GACAGAGCAGATAAT[C/T]GGAATGAGTCAGGGG | 23092 |
| rs190777297 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985974 | ATAAACATACGTGTG[C/T]ATGTGTTTTTATAGC | 23092 |
| rs190778813 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169345 | CCATTGTGCAGGAAC[A/G]TTTGTATTCAGGCAT | 23092 |
| rs190783046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152240 | CTTTAATAATAATGA[A/G]CCAATATAAATATTG | 23092 |
| rs190784984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105685 | TCCTGGCGGGAGTGG[C/T]ATCTGTCTGCATGTC | 23092 |
| rs190785276 | snp | A/C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065718 | CCCTTCCTGCAAGTG[A/C/T]AGCCTGGTAGCCTGG | 23092 |
| rs190787458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966799 | TACATAGGTATACAT[A/G]TAATGAGTTATCTTT | 23092 |
| rs190797129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917772 | TCCTGGGCTCAAGCA[A/G]TCTTCCCACCTCAGC | 23092 |
| rs190804690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025059 | CCTGGTATTATCGGC[A/C]ATGATTAAATGTTGC | 23092 |
| rs190806673 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045850 | TGAAAATACAAAAAT[A/T]AGGCTGGGTGTGGTG | 23092 |
| rs190806938 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937124 | GCAAAAACATATATC[C/T]GATAAGGGACTTATT | 23092 |
| rs190815436 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956853 | TGAGGAGGAAGCAAA[C/T]GCAGAAACCCCTGAT | 23092 |
| rs190822646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008674 | CAGATTTTGATCCAA[A/T]GTGTGGTATGGCTAA | 23092 |
| rs190842950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846820 | TCATTAATTCAATAT[C/G]TATTGATTAGTATGC | 23092 |
| rs190859232 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882715 | TCCATGTGGTAGGCA[A/C]CCTGCCAAGCACTGT | 23092 |
| rs190865412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951797 | TGAACAGACCACGAG[C/T]GGAATACCTGAGTTG | 23092 |
| rs190876637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922752 | CAGTCCTACTTTTCC[C/T]TCCTGGTGCAACGTG | 23092 |
| rs190883335 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838340 | TAACAAGGAAATAGG[A/T]TTTGCATTTTTCTTC | 23092 |
| rs190893473 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166750 | TCATCTGTAGCCACA[C/G]TGAACTGGGTTACCA | 23092 |
| rs190894008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774658 | GATTTTGACAAATGT[A/G]TAATGACATATAAAC | 23092 |
| rs190905845 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877050 | GTATTTGGGGGTGGG[A/G]GTGTGGCAAGCAAAT | 23092 |
| rs190913390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186506 | TGCTACAACATCAAG[C/T]CTCTCTTTGATAACA | 23092 |
| rs190913886 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795153 | TTGCCTACCCCCAGA[A/C]TGGGTTTTGGAGTCA | 23092 |
| rs190917542 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214177 | TTCAAAGCTCCTCCC[G/T]AGGGAAAATCTCAAT | 23092 |
| rs190935721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814309 | TAGATGTGCTGTAAA[C/T]AGCGACTGCCTACAA | 23092 |
| rs190955912 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948103 | GTTTCCCTTTTCAGA[C/T]GCGGGCTTTGATGCG | 23092 |
| rs190958712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064927 | GCTGTTAATGTTCAG[C/T]AGTCTTAGAGCTCCT | 23092 |
| rs190961046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020523 | AAATGGAAATTTCCT[C/T]CCTTCTCTCCTCCCC | 23092 |
| rs190967458 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024152 | GAGAGAGAAGAAGGG[A/G]CAGGAACAGCTTGTT | 23092 |
| rs190981375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104276 | GCACTCTGGGAAGCC[A/G]AAGCAGGTGGATCAT | 23092 |
| rs190984863 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989941 | TGTGTCTTGGAGTCG[C/T]TTTTCTCGAGCAGTA | 23092 |
| rs190987748 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079551 | AGGGTGTGCCAGACA[C/T]GGGACAACCAGCCTG | 23092 |
| rs190990416 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203657 | GTTCACAATAGCAAA[A/G]ACTTGGAACCAACCC | 23092 |
| rs190992515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185644 | TCCACTACTTTATCC[A/G]GTTCAGCAAGTATCA | 23092 |
| rs190994301 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143881 | ATATGTTTGTGAAAG[C/T]ACTGCCAATGCATGC | 23092 |
| rs190994583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775007 | TTTTGGTCGTTTCCA[A/G]GTTTTATCAATTATG | 23092 |
| rs190997266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104888 | AATGTGACACGTATA[A/C]CTTAAAACATTGAAT | 23092 |
| rs191009122 | snp | C/T | 0.000700734 | 0.018705 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222349 | GCTTTCTCTCCCCTT[C/T]CTGTACAGTTCACCC | 23092 |
| rs191011422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065423 | CAATTGTGGCTGAAA[C/T]GTGGCAGCTGGCAGA | 23092 |
| rs191014907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149084 | TTGGGATTTTTTGTT[G/T]TTTAGGTGTCTAGAT | 23092 |
| rs191026987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165842 | ATTTCTGAGTACGAC[G/T]AACAGTTCCTTGCCC | 23092 |
| rs191038789 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201798 | CGACATGCATCTTTG[C/T]AGTACATAAAATGTG | 23092 |
| rs191041729 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967318 | TTCAGTGTCAAGCGG[C/T]TAGAAGGTGTATGTG | 23092 |
| rs191042932 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768687 | CTTTAGGTGCTCAAG[A/G]TAAAGCATTAAACAG | 23092 |
| rs191049349 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218318 | ACCTAAAATTATATG[C/T]TTGCTTATTGCTTGA | 23092 |
| rs191068534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791836 | AGGCATGGTGGCACG[C/T]GCCTGTAGTTCCAGC | 23092 |
| rs191075120 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800869 | AGGAAAGCGGAGGCC[A/G]TGGCAGAGAGAGATC | 23092 |
| rs191081942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810313 | GCTAAGCTACCATGT[A/G]TACAATAATAGTCGA | 23092 |
| rs191088353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817132 | AACACTCAGCATGGT[C/T]CTGGAAGTGTGGGAA | 23092 |
| rs191109041 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834407 | GTTTTTAATCATTTT[A/G]GAAACTTATTTTAAA | 23092 |
| rs191116996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874783 | GACAGGAAATCCTTC[A/G]ACTCCTAAGCGGAAC | 23092 |
| rs191121208 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857892 | TGCATAGGAATCATC[C/T]GGAGAGTTTATTTTA | 23092 |
| rs191135581 | snp | G/T | 0.0777841 | 0.181223 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893942 | GGTATTATTTGTGGG[G/T]TTTTTTTTTTTCTGT | 23092 |
| rs191139437 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820122 | TGTAGCAGTGGAAAT[A/G]GAATCCACGAATGTG | 23092 |
| rs191139854 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914655 | TATCCTTTACTGTGT[A/G]TAGAGGTGTGAGAGG | 23092 |
| rs191140603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860237 | CATTAAGCCAAGCAG[A/G]CCCTTCTGAGCATGG | 23092 |
| rs191142998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930761 | TTTACATGCCCACGG[C/G]TCTAAATTTTTAAGG | 23092 |
| rs191149671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150060 | TGAATGTAATGCTAA[A/G]TCAGGCATCAAAATT | 23092 |
| rs191150296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209321 | TTCCTTCCTACTTCT[G/T]CCTACCTCCCAAAGT | 23092 |
| rs191152990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953716 | TGAGGTAAAACTTAT[G/T]GAGTGCCAACTGACA | 23092 |
| rs191158127 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896657 | CCATTTCCTGGCATC[C/G]TGTTGTAGTGTGTCC | 23092 |
| rs191198749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926237 | GGGTAGCAACTTGCC[C/T]TGTAATAGATGGAGA | 23092 |
| rs191203304 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039765 | TAGTAAATGCAAACT[A/G]GTAGCTCAGGAGGAC | 23092 |
| rs191216263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156784 | CCCGTGGCCTTTGGG[A/T]TCAGTCACAGCTTAT | 23092 |
| rs191222651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816278 | GCAGCTGAGAGCAAC[A/T]TGGTGCATGATCGAC | 23092 |
| rs191224763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222151 | AGCTTTCATCAGAAG[A/G]CTTATATTCCACAAA | 23092 |
| rs191225977 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002764 | ATCCAGTTTTTGTTT[A/G]TGTTGGCTGTGACTC | 23092 |
| rs191228331 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123231 | TGAGAACAGAACATG[C/T]ACATTACTCTGGGAA | 23092 |
| rs191228410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775722 | TTATGAGTGGAATTA[C/T]ACAATATTTGTCATA | 23092 |
| rs191242799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880738 | TACTTTGTGTGGATT[G/T]TGCTTAGTTGCAAAA | 23092 |
| rs191253981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184940 | TATTTTGACTCAGCC[A/G]CTGCACCCCTAGTAT | 23092 |
| rs191256334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856381 | CCTATCTTGGAAGAT[C/G]GCTGTTTGGCCAGTG | 23092 |
| rs191257087 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088537 | TAACATTTAAATTTC[A/T]TGTGAAGCAGAAAGA | 23092 |
| rs191258360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119738 | TTCATAAACCTAACC[A/G]TGCTCTGCCCACCTT | 23092 |
| rs191260193 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921735 | TACTAGCTGTGTGAC[C/T]CTGGGTAAGTGGTTT | 23092 |
| rs191263546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045373 | ATATCCATGATTCTC[A/C]CTACGAGTTAAATAA | 23092 |
| rs191268231 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892047 | GCCTGTCCTGGACAC[A/G]CACCTGCACAGAGGG | 23092 |
| rs191270467 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083113 | GAAGCTAGAGCTGGA[G/T]ACTTTTTCTTCGTCT | 23092 |
| rs191277270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198122 | TAGTAGCACTATTGC[A/G]TCCCTTTTATTTGTA | 23092 |
| rs191280076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961819 | TGATCATCTTTTAAT[A/G]TCCCATTTGAAGTGT | 23092 |
| rs191284905 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957556 | CACTACATGTGCATA[A/G]TAGACAGTAGGTTTG | 23092 |
| rs191284960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909109 | GGAAAATTCTCACCA[A/G]TTATCCCTTTGAGTT | 23092 |
| rs191292177 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928196 | CCAATTTTTCAATAT[C/T]TTTTCTTTATGATTA | 23092 |
| rs191292866 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215139 | CCTTGCAGAAGACAA[A/T]CCAGAATGGGCTGCG | 23092 |
| rs191310732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141698 | ATCCCAGTCAACTGT[A/G]AGTTAACGGGAAACC | 23092 |
| rs191320164 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980337 | TGAGCTATTGTGCAT[A/T]AAGCCTCTAGGAACC | 23092 |
| rs191321213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179429 | GGATCTCCTGGGTTG[C/T]GTTGCTTTTTGTGAC | 23092 |
| rs191321995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780616 | CAGCAAAAATCATTC[C/T]CTAAACTGAGACAGC | 23092 |
| rs191327297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157865 | CCTGTGTGGCCTGAT[G/T]GTGGATCTACCAGGG | 23092 |
| rs191360509 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227841 | TTTAGAAGGATAAAT[A/G]TTATGCTTACTGAGG | 23092 |
| rs191377921 | snp | A/T | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965709 | ATTCTTGTCTTATAT[A/T]TTATTATACTGGAAC | 23092 |
| rs191391945 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191935 | GCTGTACCGTTTTAT[G/T]ACATCAGATAATTCT | 23092 |
| rs191393779 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897232 | TCGTAGTGTGCAGAT[A/G]TTTTTCAGTTCATAC | 23092 |
| rs191400679 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159874 | GATGGTGATCTGTGG[C/T]GGAAGGAACACTGCC | 23092 |
| rs191415740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788432 | AGAGTGTCACAGAAT[A/T]ACAAATTTCATATGT | 23092 |
| rs191417980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936088 | AGATAACACAATTGT[C/T]TATGTAGAAAATCCC | 23092 |
| rs191436298 | snp | A/T | 0.0218839 | 0.102289 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029571 | CACCATGCCCAGCAA[A/T]TTTTTTTTTAACCTT | 23092 |
| rs191440024 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052320 | ACTAAAAATACAAAA[A/C]TTAGCTGGGCATGGT | 23092 |
| rs191444999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203486 | CTGGGGTTGTAAATT[G/T]GTTCAACCATTGTGG | 23092 |
| rs191454479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013306 | ACCTACATAATGTCA[C/T]TGATTTTGCCTCTTG | 23092 |
| rs191458596 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993669 | TTTGAGACAGGGCCT[C/T]GCTCTGTCACCCAGA | 23092 |
| rs191465951 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795858 | AAGTTATGATGGAAT[A/G]GATAGAAATCATGTG | 23092 |
| rs191466338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977682 | TGCTAGCCATCTCCT[G/T]GTTAAGAAAGAAGAT | 23092 |
| rs191466737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201300 | AGCTTAATACACCCA[C/T]CTGGACTCTGAGGGT | 23092 |
| rs191468398 | snp | C/T | 0.097727 | 0.198275 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890114 | GTACTCCAGCCTGGG[C/T]AACAAGAGCGAAACT | 23092 |
| rs191471731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833264 | TGGCATTTCACCATG[C/T]TGACCAGGCTGGTCT | 23092 |
| rs191474389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937582 | GTTCGCACAAAAACC[C/T]GTATGCATAAACCTC | 23092 |
| rs191488011 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139125 | GGTAAAATGCTGAGG[C/G]GCTGGGGTGGAAGTA | 23092 |
| rs191488162 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100579 | AGCTTAATCACCTCC[C/T]ATGGTGTGAATTTGG | 23092 |
| rs191490858 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047676 | TATCTTTTTAAATTT[A/T]ATTTTGCATTTCTGT | 23092 |
| rs191492851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055734 | TGCTGTTGTTGATAG[A/G]TGAGTCACTGACTGA | 23092 |
| rs191494331 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165437 | CATGTCACCTCATGC[A/G]GGCTTCGGTAAGAAC | 23092 |
| rs191494868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026672 | ACCATGTGGGGCCAG[A/G]AGATAAGACTGCATT | 23092 |
| rs191499814 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010556 | AAGTCCTGGTAAGCA[G/T]GATTTGTTAGCTTCA | 23092 |
| rs191500124 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079762 | TTAGCATGGTAACAT[A/T]GGTGGAAATTGATCC | 23092 |
| rs191503410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872986 | CTAGGGGAAATTACT[C/G]TTGAGTCAGACTTGT | 23092 |
| rs191508643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940661 | GCTGCATAGTATTCC[A/G]TGGTGTATATTTACC | 23092 |
| rs191513114 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991419 | CACTTCCCAGGTAAG[A/G]TGATGCCTTGCCCTG | 23092 |
| rs191516231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791309 | GAATCAGAACTAAGT[A/G]TAGATTAATGCTGTC | 23092 |
| rs191516617 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061009 | CCAGTTTTGACTTTC[A/C]AAGTCTTTGCAATTT | 23092 |
| rs191519529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973462 | ATATAAATAATTTCT[A/G]GAGATGATACTCAAA | 23092 |
| rs191527111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976419 | CAGATCTCTTGATCC[C/T]TATTTGGCCCTTTTG | 23092 |
| rs191527964 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101808 | ATTTAACTGGACAAG[A/C/G]TAGGGAGAGAAGCTG | 23092 |
| rs191534253 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121375 | GTTATGGTGGTGGCA[A/G]TGGTGGGTAAAATTG | 23092 |
| rs191535883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783073 | CCACACATTAGGTCT[A/G]AATAGGTCAGCAGAG | 23092 |
| rs191549516 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827226 | CTCTGGTGTTGGCTG[A/G]CCTCCATGGTTGGTT | 23092 |
| rs191623939 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933526 | GTGTATTTCTCTCTT[A/G]GAGCCGAGAAGGGAG | 23092 |
| rs191630189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954041 | ATATATGGCACGCAA[A/G]TATGCTGTCTGAGCA | 23092 |
| rs191659698 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916790 | CCTGCCTTTTTAAAG[A/G]ATGTGAAAATGGAGG | 23092 |
| rs191675100 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956383 | AAATTCAAGACCAGA[A/C/T]TGGACAACACAGCAA | 23092 |
| rs191687054 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166920 | AGGTGGTTACATTCA[C/T]AGAATAGAAAGTTAA | 23092 |
| rs191693327 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160246 | TTTTATTTTTAGTAG[A/G]GATGGAGTTTCACCG | 23092 |
| rs191696157 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883992 | AAGAGATGTGTCTGA[C/G]CTTCTTTATTTGGCC | 23092 |
| rs191697218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806512 | GTGTGTGTGTGTTTA[A/G]TTTAAGTTGGTTGTT | 23092 |
| rs191703102 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902929 | TGGACTCGCAGAGGG[G/T]GAAATAGAGCTGTGA | 23092 |
| rs191703378 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194909 | GCCAGCGGGAACACA[C/G]GGAGAGTGTCAGGTT | 23092 |
| rs191709744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210921 | GCAGCCGAAAACTAC[A/C]CCAGGCCCTCTGTAT | 23092 |
| rs191721254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110713 | AATTACATTGGACTT[C/T]AGAATGAATTGTTAT | 23092 |
| rs191726233 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150275 | ACCCATGCATGCCAA[C/G]CTACCTGGGGTAAAC | 23092 |
| rs191727731 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217453 | CATATTCTCAGGAAC[A/G]TTAGTCATCTTGAAG | 23092 |
| rs191732144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219835 | GTGCAGTTTGAATAA[G/T]CATCCTGAGGGTTCC | 23092 |
| rs191732696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130059 | GGCAGTGATGTCAGC[A/G]TCAGTGATGGTGAGG | 23092 |
| rs191742868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092940 | TGTCTTTTTCCCTCA[A/G]TCACCGGGGAGGAAC | 23092 |
| rs191746394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021202 | ATGTATTTTGTCAAT[A/G]TCAGTATGAATTTTA | 23092 |
| rs191752214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052606 | GAGAGCCACATGTTT[C/T]TGAGCTGGGGACCCT | 23092 |
| rs191754267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074320 | GATCCACTGACTTTT[C/T]GTCCATTATAGAACT | 23092 |
| rs191759568 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095223 | TTTTATTGAGGTGAA[A/T]TTCACTTAACATAAA | 23092 |
| rs191773767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055507 | ATGGTTAAACATACT[C/T]ATACCCCAGCAGGTA | 23092 |
| rs191776800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992721 | ATGAGTCACCACGCC[C/T]GGCCAGTAGTGATTT | 23092 |
| rs191779995 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990480 | TCAAAGTCATTCTCC[A/G]TCTAGCTTTGTTCCA | 23092 |
| rs191780172 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016651 | GAGGTTGCAGTGAGC[C/G]AAGATCGTGCTATTG | 23092 |
| rs191787987 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137933 | ATTTGCCTCTTCCTT[C/G]CCAGAGAAGAAGCTC | 23092 |
| rs191792162 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110029 | AGCATGCCACCCAGG[C/T]ACTTACCCCGAGGTG | 23092 |
| rs191792777 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809334 | TGTAAATAAAAGTTC[C/T]CCAAGAGAGAAGCCA | 23092 |
| rs191803600 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073165 | CTCCTTAGGTGATGA[A/G]GGGAATCCAACTGAA | 23092 |
| rs191822083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851789 | CTTGTGCACCTGGTG[C/T]TCTTTCGGCATGGCC | 23092 |
| rs191825181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029145 | TGTGTGAAAATTGGA[A/G]ATTATTCTTCAGGTG | 23092 |
| rs191837124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824893 | TGGCAAATGTTAAAT[A/G]TATATTGAGGATCAT | 23092 |
| rs191840359 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788913 | ATTTCATTGAACCTT[C/G]ACAACAGTCTTAATG | 23092 |
| rs191842829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807989 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCGAG | 23092 |
| rs191845038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847436 | GATCTCGGCTCACAG[A/C]AACCTCTGCCTCCCG | 23092 |
| rs191845963 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993263 | CAAGCTCCGCTTCCC[A/G]GGTTCACGCCATTCT | 23092 |
| rs191860852 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864437 | AAAAAATGGTCCATC[A/C]GGGTTTTGCCTTGCC | 23092 |
| rs191860995 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142972033 | CTAAAAATACAAAAA[G/T]TAGCTGGGTGTGGTG | 23092 |
| rs191872719 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831253 | GATATCTCTCTGCCT[C/T]GTTCAGGTGCTGAAC | 23092 |
| rs191880885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996696 | GATTTGAGGTTAGGG[G/T]AAATTCCTAGATGAA | 23092 |
| rs191932251 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199102 | ATAAGAAACCGAACT[C/G]TGTCATTGTTTAAAT | 23092 |
| rs191939174 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229043 | AGTTTGACTCAATAC[A/C]TGCTTTAATATGTCT | 23092 |
| rs191941789 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209601 | GCCTGGACAACGTGA[C/T]AAAACCCCATCTCTA | 23092 |
| rs191951910 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215968 | TCTCTTGGGGATATA[C/G]CTAGGAGTGGGATTG | 23092 |
| rs191963226 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173554 | TCAGGCACTTCGCTT[A/C]GCAATTTACATAGGC | 23092 |
| rs191969052 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226783 | TCACCGAGTGCTTTT[C/T]GGTGAGAGGCAAAGA | 23092 |
| rs191970171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153409 | GGGTCGTTCAATGGG[C/T]GCTTACTGAGGGCTG | 23092 |
| rs191970788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784430 | TGCTTGAAACCGTAC[A/G]TAATTTGTACATGAA | 23092 |
| rs191972772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107722 | ACTTCACTCTGAATC[A/G]TTCGGTGTCTTTGTT | 23092 |
| rs191973007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822332 | TTCTGGTGACATACA[C/T]GCTGGGCTCTGTTAA | 23092 |
| rs191974567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192767 | CATGGTGGATCTAAC[A/C]CTCAGCACATTTGGA | 23092 |
| rs191978468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779486 | TTGAGGGGTTTGTGA[A/G]TTCCACACCAAACTG | 23092 |
| rs191979037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146167 | TCTGTAATAAATAGG[A/G]GACAAGAATCACATT | 23092 |
| rs191979829 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804080 | TGGGATGGAGCCTGC[A/G]GCCGTAAAGTCAGCC | 23092 |
| rs191982261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855415 | CTTAAGGAGGCTCTC[A/G]TATCTTTTGCACTTT | 23092 |
| rs191983191 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125812 | TTTATATCCATCATT[C/G]AATTTTCACAGCAAC | 23092 |
| rs191988133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190521 | GAATTTTATGATCAG[A/C]AAAACTATTCTTCTC | 23092 |
| rs191988830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144714 | TGCTTGGCTCATTTT[A/C]TCCTTATTTCCTAAT | 23092 |
| rs191992486 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843502 | GTGCCAGACATGCCA[G/T]GCAAACCCACGTGCT | 23092 |
| rs191993689 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182070 | CTGCTGCCTCAGAAG[G/T]TTCTTCCCTGATCCT | 23092 |
| rs191993896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888375 | ATTAGAGAGAGGGAA[A/G]GACCTTAGTGATCAT | 23092 |
| rs191994070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908071 | TATACAATATCAAGC[A/G]TATCAAATATTTTTA | 23092 |
| rs192000234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862633 | GTTCTGGGTTCTGTC[C/T]GGGTGCGTGGGCCCT | 23092 |
| rs192002097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879299 | ATGGGGAGGCATCTC[A/G]TGCTGGAGCTGCTGT | 23092 |
| rs192002482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926530 | TTTTTAGAATTTGCC[A/C]AAGACCCCTTCTCTG | 23092 |
| rs192005492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824171 | ATTTGCTGCAGTTCG[C/T]GTTCCCATGCTCTGT | 23092 |
| rs192011196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852332 | GGACCTCATTGTCCT[C/T]TGGGGACATGGAATT | 23092 |
| rs192014616 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948696 | AGGTTAGAAGGGGAT[A/G]TAAAGCAAGAAAACA | 23092 |
| rs192016895 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115420 | TTCAAAGTATTTCAT[A/T]TTTTTTTTTTACACC | 23092 |
| rs192021558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888152 | CTCACCCTAAGAGGT[A/G]TAGATGTGGTTACTA | 23092 |
| rs192021809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152463 | GAAGAGTTGGTTACA[C/T]TAAACCTATGTGAAA | 23092 |
| rs192034501 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925944 | TGTTTCAGTGGGGTG[A/G]AGTTAGTAATAGCTT | 23092 |
| rs192041118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114859 | AATGGTCAGTGGAGT[A/G]CTCAGAACTGTTCTT | 23092 |
| rs192053512 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078998 | GTAATTTCCAGCTGG[A/G]TCAGTAAAGGATAAT | 23092 |
| rs192055233 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083304 | GTAACCGGCCTAATG[A/G]TCAGTTTTACTCCTG | 23092 |
| rs192077666 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004166 | TGAGGTATGGCTGCT[C/G]GGATTGGCCAAGACT | 23092 |
| rs192079529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034137 | AATTGGAACCCTCGT[A/G]CATTGCGGGTAGGAA | 23092 |
| rs192081805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986444 | TTGTAAAAGTTCTCT[C/T]CCATTCTGTAGGTTG | 23092 |
| rs192089386 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968288 | CAGAGCATCTGGTAT[A/G]AGAGCCAGTGCTCTT | 23092 |
| rs192100881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117908 | ATCTTTTATTGCCTT[A/C]GTGAAAGCTCATTGT | 23092 |
| rs192102793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156042 | AGGCTTAAGATTTCG[C/T]ATGGCTTTTTCAACA | 23092 |
| rs192105179 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091840 | CAATATGTTTACACA[C/T]GGAATTTCCTTTACA | 23092 |
| rs192113135 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051886 | CTTGGGTAGAAGTTG[A/G]TTTCTTCTTTAGAAA | 23092 |
| rs192146573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797857 | TCCAGATTGCCTGGG[G/T]ACCTTGTTAAAATGC | 23092 |
| rs192153833 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977126 | AGTACACTAAAGGAA[A/G]ATTGAGAAGTTTTAG | 23092 |
| rs192159746 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945247 | GATATGGGTCTCTGC[C/G]TGGCTGACGTGTGTG | 23092 |
| rs192170708 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787197 | AGTGGCTTATTTTCT[A/C]CCTCTCTAATGGGAC | 23092 |
| rs192202961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090102 | CTAAGTTTCCTCCCT[A/G]TCGTGAACTTAGTGT | 23092 |
| rs192212008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945470 | TCTTCTCTGAGGAGG[C/T]TGGTGTGAGGGAGGC | 23092 |
| rs192219283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796790 | ATGGGTTTCCCAGCA[C/T]CAGTCCACTGAATAT | 23092 |
| rs192223073 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070676 | GCACTTTGGGAGGCC[A/G]AGATGGATGGATCAC | 23092 |
| rs192223461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009393 | TCTGGAGACAGACCG[A/T]GGGAGTTCCTGTCTG | 23092 |
| rs192224540 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776575 | TAGCATGTATCAGTA[C/G]TTTGTTCCTTTTTAT | 23092 |
| rs192230532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816511 | AGTGGAGAAGCAAAG[G/T]CATCTTGTAGGAGAT | 23092 |
| rs192242223 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972871 | GACCTTTATTCTTTT[C/T]TTTTTCAGATTTTAC | 23092 |
| rs192245327 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833656 | TACCTACCGCTGATA[G/T]TTGCGCTCTTTCTGT | 23092 |
| rs192306762 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824611 | GATTAAAAGGAGGTT[C/G]ATTACACAGCCAGCA | 23092 |
| rs192317557 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800302 | TTCCTCCCCCTCTCT[C/G]TGTCTCTGTCTGTCT | 23092 |
| rs192319376 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864710 | AAAGCAAGGCAGGGC[C/T]GGGGGCATCCCTGTC | 23092 |
| rs192319623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999159 | ACAGAGAGACGAAGA[A/G]GTTTGATCCGGGTCC | 23092 |
| rs192326388 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983628 | GCATTTTTACATCGA[A/T]AAAATAAACTATATT | 23092 |
| rs192327666 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885127 | TCTCTGCTAGACACT[C/G]AAACTCAGGGGGCTG | 23092 |
| rs192329713 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171400 | TAGCCCTAGATGAGA[C/G]CCGCACTTGAGATCT | 23092 |
| rs192331259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208805 | GATGATGGGAAGGAG[A/T]TTTTCAGTAATTCTT | 23092 |
| rs192334967 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965303 | CCCTCCACAAGAGGT[A/G]GAGGAGCAGAGTCTT | 23092 |
| rs192336152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827824 | ACCCTTAGTGTTTCA[A/G]ACAGTGTCTGGCACA | 23092 |
| rs192338815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949850 | TGTTGGCATATGGAC[G/T]TGCTAAGGAGAAAAG | 23092 |
| rs192339974 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904112 | CCCAAACAATCATGA[C/T]TTAGGCCTTTTTCCT | 23092 |
| rs192348348 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062722 | AGTGGTTCAGTAGCA[C/T]TCCTTGAAGTTCTTA | 23092 |
| rs192351046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132695 | GTGTGGCAAGGACTC[A/T]GTAAACCATAGCTAC | 23092 |
| rs192355293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083574 | CACAATCTTGGCTCA[A/G]TGCAATCTCCGCCTC | 23092 |
| rs192358398 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041741 | AAAAAAAAAAAAAAA[A/C]GTGCATTTGGCTGGA | 23092 |
| rs192365769 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, splice-donor-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867856 | GTTTGTCCTAACTTA[A/C]CTGCTTTTTTTTTCA | 23092 |
| rs192376512 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022290 | GTTGGCCAGGCTGGT[C/T]TCGGACTCCTGACCT | 23092 |
| rs192378896 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004325 | TTGCTTTAACACAGA[A/C]CTTAATGCCAAGTTT | 23092 |
| rs192379234 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095781 | TTTCACCATGTTGGC[C/T]AGGCTGTCTCAAACT | 23092 |
| rs192383394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907089 | TAATCTTGAGGGACA[C/T]AGTCCTTAGAGGTTA | 23092 |
| rs192392476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987049 | GTGAAGAAAGTCATT[G/T]GTGGGGATGGCATTG | 23092 |
| rs192400831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946789 | TTGAGAGAGCTTATG[A/G]TGCCAGTTTTACTGC | 23092 |
| rs192404374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206794 | CATTTCTGCTGAGAC[A/G]TAACCTGAAAAACAC | 23092 |
| rs192404490 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224498 | TCAGGATTTAAATAA[A/G]TGGGGTCAGGCATTC | 23092 |
| rs192425403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167657 | GTATGGGGGCAAGCG[C/T]ATGACTAAGCCAGGC | 23092 |
| rs192433015 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769339 | TTATTCAAGGACAGT[C/T]CCTATCCTCCAGGAG | 23092 |
| rs192437372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129584 | AGGTCCCAGTCCAGC[G/T]GCACTCCTTATCTAT | 23092 |
| rs192441365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187851 | TTAGAAGCAGGACTT[C/T]GTGTTGTTGCTATGT | 23092 |
| rs192446949 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092232 | GCAGTGGCACGATCT[C/T]GGCTCACTGCAAGCT | 23092 |
| rs192448485 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803655 | GGAATGGAATCATAA[A/G]AATCCTCCTGCAGCA | 23092 |
| rs192453467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063339 | CTCCCTATTGCTCTG[C/G]CTGGTGGAGCTCTGG | 23092 |
| rs192457062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150999 | CCACACACTAGGAGA[A/G]AATATTTGCAAAACA | 23092 |
| rs192469127 | snp | A/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022365 | GGCATGAGCCACTGC[A/G/T]CCTGGCCAATCCCCT | 23092 |
| rs192481903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842318 | ATTGTTCTTGAAAAG[A/T]GAGGAGTGTGGAGTT | 23092 |
| rs192483873 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988196 | CTATTCAGGGATTCA[A/G]CTTCTTCCTGGTTTA | 23092 |
| rs192486204 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878515 | GCCTTTACAAGATAC[C/T]GATGTGTATGTGTGT | 23092 |
| rs192503443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120453 | TATGTTTAATCTGAT[C/T]GGCCTTTAATACTTT | 23092 |
| rs192506060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918527 | GTTTTACCTTTGATA[C/T]CTAAAAAGTAGACCT | 23092 |
| rs192514244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101220 | AGAGAGTTAGGAAGG[A/T]ATGAGAATGAGTCTG | 23092 |
| rs192525629 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182535 | AGTGAATCCGTTTTA[G/T]TTTAAAAAAACAATA | 23092 |
| rs192542783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145376 | CCTGTGAAGCAGTAA[A/G]TGTCTCCAGTTGAAG | 23092 |
| rs192548512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035634 | TCTCACAAGTCACCA[C/T]TAAGGAACTTATCCA | 23092 |
| rs192551577 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214314 | TGGACTAGTGTAATC[A/G]GCTCCATGTTGAGTT | 23092 |
| rs192552009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097512 | TTCTGTTGAAGCAGA[A/G]CTAATGTGAAAATTG | 23092 |
| rs192553883 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160995 | ACCCCAGCCTCTGGG[C/T]TATTTCAGATTTTTT | 23092 |
| rs192558462 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106906 | CTTCTGGACTGCACT[A/G]TTTGATTAATGGGCT | 23092 |
| rs192562746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056711 | AAAGGGGCAGAAAGA[C/T]TCTCTATCAGATTTA | 23092 |
| rs192562904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080913 | GGGGCCTGGACTAGG[A/G]TAGTAGTGGTGGAAA | 23092 |
| rs192565381 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840543 | AAGTCATGTGGAAAA[A/G]ACAGACAGTAAACAA | 23092 |
| rs192567290 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125180 | TTTTTCAATAGAAGG[C/T]AAGAGACCTCTGTGT | 23092 |
| rs192570200 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998287 | AGCTGTGGAGCAGGG[A/C]TGAGTAGTAGGGCCA | 23092 |
| rs192571876 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793680 | GCAACCTCCACCTCC[C/T]GAGTTTAAGTGATTC | 23092 |
| rs192575519 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142771554 | AGCAGAAGGTGATAG[G/T]GGTGGGAGTAGAGAA | 23092 |
| rs192576083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036515 | TTCTTGGCTCTTTTA[A/G]TTTTCCTCTGAATCA | 23092 |
| rs192577734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018580 | TTAGTTTTCCTATCA[A/G]CATCTACTAAGCTAT | 23092 |
| rs192578290 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828972 | CCTGTTAAAGTGTTT[A/C]TGTGTGCTCATGATC | 23092 |
| rs192585191 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965023 | GTCATGTGGGTCACA[C/T]GTCCACTGGACAAGG | 23092 |
| rs192588125 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861172 | GAGCCTGGGGATTTC[A/G]TGGGCACCTATGAGG | 23092 |
| rs192588532 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000292 | ATTTACCTAAGAGAA[A/G]TGAAAACACATGTCT | 23092 |
| rs192590600 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812855 | TAAAACAGGGGTATT[A/G]ATGCTGGGCCTTAGC | 23092 |
| rs192592917 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984286 | ATTCCTAAGAGGAGT[A/G]TGTGTTTTCAGCTGG | 23092 |
| rs192598257 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877791 | GTTGGAGTGTAGCCT[A/G]AACTTAGGGATTTTA | 23092 |
| rs192603742 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898011 | CTCTATGCAAATCGA[A/C]CGTGTTCATTTGTTT | 23092 |
| rs192625257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858453 | ATTGTTTTGTGTGTC[A/G]TGAAGGAGTGAGTAA | 23092 |
| rs192637510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965688 | AGATCTACATCTGGT[A/T]TAACTATTCTTGTCT | 23092 |
| rs192640570 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923500 | TGCATTCTCCTTGAG[C/T]CTCACTCATCCCATC | 23092 |
| rs192642123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894179 | TTTCTGACCTGCTTT[C/T]GGAATGCTATCCTTG | 23092 |
| rs192643863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990863 | CTGTATCAGTTGTCA[A/G]TCGGCCCCTACTGAG | 23092 |
| rs192656361 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183050 | GGGTTATTCTCCTTA[C/T]GCCTCATGCAAATGA | 23092 |
| rs192687236 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145661 | GTTTCTCTTTGTTGT[C/T]GTTTCTGTTCAAAAA | 23092 |
| rs192693202 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107268 | TTGGAGGGGTCAGTA[G/T]GCAGGGGCTGGATCG | 23092 |
| rs192702002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143069129 | AATGAGGTCTTCCTC[A/G]ATTGTTTTAAGATTG | 23092 |
| rs192703431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806955 | GGCTTTGATATAGAA[C/G]AGCAGCACTGGATCC | 23092 |
| rs192703615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777398 | CAAAATGAGAACCGG[C/T]CAAGGAAGAACTGTT | 23092 |
| rs192714251 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121720 | TCCTAGTCTTTCTTT[C/T]GAAGGTTTTCCTCAT | 23092 |
| rs192716330 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158397 | GTCAAAGCCCCCTAC[A/C]CTATTGTTCCTCCGT | 23092 |
| rs192718278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186770 | TTGGGGAGCTTTGCT[C/G]TGCAGACACAGTGAC | 23092 |
| rs192749335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013553 | CAGTTCCCACTCCCC[A/G]GTATTAACAGTCAAC | 23092 |
| rs192772210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084217 | CACAGTATTCCCTGC[C/T]ATTAAAACTTAATCC | 23092 |
| rs192782725 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110298 | TCTGTCTTGTTCACC[A/G]GTATATCTCCAGCAC | 23092 |
| rs192786704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042600 | ACCTAAATGGCAAAC[A/G]GATCAGGTTTCACAG | 23092 |
| rs192786946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821759 | TGCCAACTCTGTGTA[A/G]GAGGAATTTTTATTA | 23092 |
| rs192790984 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861590 | CAAAGTGGTAGGGGC[C/T]GGGTGGCTTCATTGT | 23092 |
| rs192791038 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005944 | ACTCGGCACCAACAG[A/G]TACAGAACCCCTTTC | 23092 |
| rs192792186 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224001 | CCCAGGAGCCCCTTG[C/G]ATGGCAGCGTTGCTT | 23092 |
| rs192801165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969566 | GGGTAGAAGAGCTCC[A/C]GTTGGATTATTTGTC | 23092 |
| rs192805294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898609 | GCACCTTCTAACACG[C/T]CAGTCTGATTCTCTC | 23092 |
| rs192808727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828486 | TGGGAAAATGAAATT[C/T]AAAAGAAAAACATGG | 23092 |
| rs192812902 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869357 | GGATTACAGGTGCAC[A/T]CCAGTACACCCGGCT | 23092 |
| rs192834095 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163477 | TTTTTTTAAGATGGA[A/G]TCTTGCTCTGTTGCC | 23092 |
| rs192834278 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899240 | AAATCACCTTCAGAG[A/G]TATTAGGACTTCAAC | 23092 |
| rs192835011 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017931 | TAAGCACTCTCTTGT[A/G]TTGTTCTCCAGAGTG | 23092 |
| rs192839637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938643 | ATATACACACCCAAC[C/T]TGAAGTATTTAATAT | 23092 |
| rs192841369 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983145 | ACACCTGTATGTCTG[C/T]GATCTCTGAGCCTTA | 23092 |
| rs192858111 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978121 | TCAGTCTTAAAAATT[G/T]TTTTTCTGCTTTAAT | 23092 |
| rs192874284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875521 | CCCCACTCTGCCCCT[C/T]CCCCCATCTTATTGA | 23092 |
| rs192876187 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943547 | TCATGATGTAATCAC[C/G]CCATAAGGCCCTACT | 23092 |
| rs192881369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915131 | CTCACTGTGGCACCT[C/T]CATCTTATTTCCACC | 23092 |
| rs192885428 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202383 | GACCTCTTCAAGGAA[A/G]ACTACAGACCACTGC | 23092 |
| rs192897055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125397 | CCAGAGAATCCATCT[A/G]TATCTTCCTCCTGGG | 23092 |
| rs192897960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162636 | ATTGCCCTTACTGCC[C/T]GCTTTCCCCTTCAGC | 23092 |
| rs192902489 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793106 | TCGAGTAGTGGGACC[A/G]CAAACAGTACATGGT | 23092 |
| rs192910915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089814 | GACTCTAATTGTGTC[C/T]AAATAGACGTAAGAG | 23092 |
| rs192913904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142049 | ACCAAAATCAGAAGT[C/T]GTTTTGCTGAAGATA | 23092 |
| rs192920903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206041 | TCTATAGGTGTTACA[A/G]CAGTAAGTAATTAGG | 23092 |
| rs192955953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030645 | AGGTTAAAAGAACTC[A/G]TCTACTCTCAGAGGG | 23092 |
| rs192958890 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834996 | TGTTCCACCTGGTTC[A/T]CGTGTGAACACTGTC | 23092 |
| rs192959619 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097078 | GCGCGGTGGCTCATG[C/T]GTGTAATCACAGCTC | 23092 |
| rs192961023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994269 | AGAAGGGCTTCCTTG[A/G]CAAGAAATATGGCAA | 23092 |
| rs192962303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134690 | AATTATATCACATCC[A/G]TTTTTCATCTCAGGA | 23092 |
| rs192974005 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808140 | CTCGGGAGGCTGAGG[C/T]GGGAGAATGGCATGA | 23092 |
| rs192975858 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056255 | AAAGGAAACAAATAG[A/G]GATTGCTAAGGGCCT | 23092 |
| rs192979096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848438 | GGTTTTCCCAGTCCC[A/G]TTTTCCTCCTTTACT | 23092 |
| rs192983036 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018272 | TTAGCCAGTTTAAAT[A/T]TGTTCTCATCTTGTC | 23092 |
| rs192983111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873649 | AGATATGTGAGGATC[A/G]GAGCTTGGGGCTACT | 23092 |
| rs192987113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913387 | TTTCTGCTTTTTTCC[C/T]CTTCTCCCCCTCCCT | 23092 |
| rs192997498 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953107 | TCCATGTAAGTTGTT[C/G]TGTGGTTTAGCTTGA | 23092 |
| rs193002797 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180314 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 23092 |
| rs193004343 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031897 | TTTTAATCCTTTTGC[A/G]GTAAGACAGCTAGTC | 23092 |
| rs193021227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853732 | CAGAGTAGCCTTGAC[A/T]CCACGTTCTCAGATG | 23092 |
| rs193025428 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220542 | GGTTGGATGGATGGG[A/C]AGAGGGCAGGGGTAT | 23092 |
| rs193028417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968823 | TGTGTATCCCTTCCC[C/T]GACAAACTGCTGGCA | 23092 |
| rs193038094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184121 | CAGTCTGAATATTAC[A/G]TTATCTATTTCAACA | 23092 |
| rs193042194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | ARHGAP26 | GRCh38.p7 | 5:142919256 | CACGAGAAGATACCG[C/T]GTTAACATGAAGGCA | 23092 |
| rs193051076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958993 | TTTTCTAATGTAATA[A/G]GGAATTATTAAACTT | 23092 |
| rs193055766 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889434 | CCTGGCCAACAAGGC[A/G]AAACCCTGTCTCTAG | 23092 |
| rs193067632 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927001 | ACAAGTAATTGAACT[A/G]CTCTATGCTACTGTT | 23092 |
| rs193068758 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214669 | ACTGTAGTCACGTCC[A/T]CAGGGGCTGCCATTG | 23092 |
| rs193083141 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139855 | GGTACTGACACACAC[A/G]CTGTGCTTTTTCTGG | 23092 |
| rs193086399 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112276 | AGAGCCAAGTCAAGA[A/G]GGAGAGGGGCTACAG | 23092 |
| rs193088184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179158 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCATTTA | 23092 |
| rs193091586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075230 | TAAAAATATTCCTCT[A/G]TTATAGGGTCAACAT | 23092 |
| rs193101651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193596 | TTACTTAACAGTGGC[C/T]CCAAAGTCCAAGAGT | 23092 |
| rs193104973 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116690 | ATCTGGAAGTGATTT[A/G]CCTCCTTCTGCCTCT | 23092 |
| rs193105870 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782507 | TTTTAAAAACTCCCC[A/G]GGTGATTCTAATGTG | 23092 |
| rs193111886 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821153 | TCCCCTATCTTTAAG[A/G]CATCTTAACTATGTT | 23092 |
| rs193116963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089129 | ATCTAACAATCCCTC[C/T]TCTTGCATTTCCTTA | 23092 |
| rs193119209 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046624 | TCCTAGAAATAGAAT[A/G]CCTTCTGTGTGTCTG | 23092 |
| rs193121897 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854079 | AAAATATTGGGGAAA[G/T]TATTATGTTTTTAAA | 23092 |
| rs193148432 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812424 | TCAGTGCAACCTCTG[C/T]CTCCTTGGGTTCAAG | 23092 |
| rs193152999 | snp | A/C | 0.00993419 | 0.0697739 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142770297 | CCGGGCGTCCTCGGG[A/C]GGCCTGAGGGTCGGG | 23092 |
| rs193185285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116431 | TAACACTCTAGGCCT[C/T]AAGATGAAACTTATC | 23092 |
| rs193186328 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080674 | GTTTGCAGAGCTAAG[A/C]AGGGGCCAGATGAAG | 23092 |
| rs193189947 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856739 | ATTGTATTAGGTATT[G/T]TAAGTAATCTAGAGA | 23092 |
| rs193191607 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789294 | AATTGTCTCTCTGCT[C/G]TCTCTACATCTGAAT | 23092 |
| rs193193360 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035786 | ACTAAAAATACAAAA[C/T]TTAGCCAGATGTGGT | 23092 |
| rs193193493 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825622 | GGTTATTATTTTTCT[A/G]TTGTAATTCCTTAGC | 23092 |
| rs193195890 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893179 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGATTGT | 23092 |
| rs193200032 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929775 | AAGTTGATGTAATAT[A/G]TGTGAGCCCCTGAGA | 23092 |
| rs193206401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014272 | TCCACCCCAACTTTC[C/T]GCCAGTGACTCCAGA | 23092 |
| rs193231341 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869741 | TAGATTCTAATTTTT[A/T]AAAAATTATGGTAAA | 23092 |
| rs193234704 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908493 | CTCTCTGTATTAGCA[A/C]GTTTGGGCTTCCTCA | 23092 |
| rs193237151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197346 | TGCAGCAAAATATGA[A/G]TTACAGATGAGAATG | 23092 |
| rs193238126 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949338 | ATATGTTCCTCTCTA[A/T]GAACAGGCTCAGGAC | 23092 |
| rs193241378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157717 | TACTATGGTAGAGAT[C/T]CTTTCAGAGAACAGA | 23092 |
| rs193246385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130662 | ACCAACAAAGTTGTG[A/G]ATAATTCAGATTCTC | 23092 |
| rs193249999 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093769 | CTAGGGGAGGGACCA[A/G]CGGGAGTGGAGCTAC | 23092 |
| rs193250581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052980 | TAAAAAGACGGAAAT[A/C]CTGACCTCACCTGGC | 23092 |
| rs193259618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174171 | GAGATTCTGTCCCAT[A/G]CAAAATAAAAGATAG | 23092 |
| rs193263199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135943 | GGGAACACTTGGAAC[A/G]GAACTGGCCTCACTC | 23092 |
| rs193268396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803171 | ATAGTGATCTGAGAT[A/G]CCAATTAAATCTAGT | 23092 |
| rs193273671 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143068615 | CTAAATCTTTCCCAT[C/G/T]AGCACATAAGCATGT | 23092 |
| rs193277892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025727 | AGAAACACTCCTTCC[A/G]TCCCAGGCAGATGTA | 23092 |
| rs199498080 | in-del | -/CAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997094 | AGCATAGCTGTTTTC[-/CAAA]AAACTTTATATATAT | 23092 |
| rs199532459 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954061 | CTGTCTGAGCAAAGG[C/T]GTTTTTAAGCGAGAG | 23092 |
| rs199546684 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907599 | AACATAGTTTAAGGG[A/T]AGGGTAGATGAGCAT | 23092 |
| rs199595309 | snp | G/T | 0.078151 | 0.181571 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163465 | TTTGTTTGTTTGTTT[G/T]TTTAAGATGGAGTCT | 23092 |
| rs199618424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080503 | TAAGCCATGACCTGA[A/G]TGAAGTGAGAGAGCA | 23092 |
| rs199634402 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088470 | TTTGGACCAAATTGT[A/T]AAAAAAAAAAAGTGG | 23092 |
| rs199637109 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986114 | TTGAACTAGTTTACA[C/G]TCCCACCAACAGCGT | 23092 |
| rs199638491 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958917 | CTTAAAAAAAAAAAA[A/G]AAGAAAAAAAAAAAG | 23092 |
| rs199648153 | in-del | -/GTGCGC | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963218 | TGTGTGTGTGTGTGT[-/GTGCGC]GTGTGTGTGTGTACC | 23092 |
| rs199656043 | in-del | -/AG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896004 | GACCTAACTTCCAGC[-/AG]TGTGGTTTCAGTCAA | 23092 |
| rs199674046 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876591 | GACCAGTCTGGAGGC[A/G]ACATAGTGAGACCCC | 23092 |
| rs199677007 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850436 | CCAGCATTAAAAACA[A/G]CAACAACAACAACAA | 23092 |
| rs199682261 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858116 | GAGAGAGAGAGGGAG[A/T]GTGTGTGTGTGTGTG | 23092 |
| rs199683282 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963171 | ATTCCATGGTATATA[-/TG]TATATATATATATAT | 23092 |
| rs199725847 | in-del | -/A | 0.418974 | 0.184249 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987539 | AACACTATGTTGAAT[-/A]GGAGTGGTGAGAGAG | 23092 |
| rs199728994 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900761 | AATGTTTAACAGGTT[-/A]AAAAAAAAATCATTT | 23092 |
| rs199750999 | snp | C/T | 3.29582e-05 | 0.00405931 | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207455 | ACAGGCCAGAAGAAG[C/T]GGTACATGAAGACTC | 23092 |
| rs199761987 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159924 | ATTTTTTTTTTTTTT[-/T]ACATGTGTGTGCATT | 23092 |
| rs199763736 | in-del | -/T | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204067 | GAACTTAAAGTATAA[-/T]TAAAAAAAAAAAAAT | 23092 |
| rs199769776 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116364 | TACATTGTGAATCTG[C/T]CACTACATTGTATCC | 23092 |
| rs199778557 | in-del | -/AC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012551 | TTTATATACATACAT[-/AC]ATATATATATATATA | 23092 |
| rs199788227 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188681 | AGGTATATTTGAAAG[A/T]GTAGACTGATGATTT | 23092 |
| rs199811506 | snp | C/T | 3.31752e-05 | 0.00407265 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901916 | TTATGTGACCTTTGC[C/T]TTTCTTCCTTCATTA | 23092 |
| rs199823054 | in-del | -/TTTT | 0.497722 | 0.0336691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157173 | TCAACACATTCTTTC[-/TTTT]TTTTTTTTTTTTTTT | 23092 |
| rs199825133 | in-del | -/CAT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799382 | ACACAGTAGCCATTC[-/CAT]TACAAATGCTTGTCA | 23092 |
| rs199828988 | in-del | -/T | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936780 | ATGGAGGAAGGATAG[-/T]TTTTTTTGAGAAATG | 23092 |
| rs199840025 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923087 | TGAACTTGTCATGGA[G/T]TTTTTTTTTTTCTTT | 23092 |
| rs199854793 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090615 | ATAGAAGAAGGGAAC[C/T]GGCTTAGAAAAGGGG | 23092 |
| rs199860499 | in-del | -/A | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085452 | GTTCCAGTTAATGGC[-/A]TGTGTGAAGGCAAGC | 23092 |
| rs199866481 | in-del | -/G | 0.0577344 | 0.159793 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095666 | CTCCACCTCCCAGCT[-/G]GGTTCAAGCAGTTGT | 23092 |
| rs199869969 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987136 | CCATGAGCATAGAAT[A/G]TTCTTCCATTTGTTT | 23092 |
| rs199873621 | in-del | -/T | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228036 | CATGTCAAAATTCAC[-/T]TTAGTCAGAACCAGA | 23092 |
| rs199910416 | in-del | -/AGCACCAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139622 | CTCCCCTCCAAATCT[-/AGCACCAA]CTACACAGAGAGCGA | 23092 |
| rs199914694 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989075 | CTCGTTGATCTGTCT[A/G]ATGTTGACAGTGGTG | 23092 |
| rs199923807 | snp | C/T | 0.432944 | 0.170387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988486 | TTTTTGTGTCTCTGT[C/T]TCCTCCAGTTCTGCT | 23092 |
| rs199924268 | in-del | -/AAAAAAAAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004018 | AACAAATTTATAGAC[-/AAAAAAAAAA]AAAAAAAAAAAGGAA | 23092 |
| rs199938617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150398 | AGTCATAATGTGTTC[A/G]GAGTTCAACCACTGT | 23092 |
| rs199958139 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923856 | TTATTAGGATCAGAT[C/T]CTTTTTTTTTTTTTT | 23092 |
| rs199968029 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992497 | GGAGTGCAGTGGCGT[A/G]ATCTCTGCTCACTGC | 23092 |
| rs199970432 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786670 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTTGAGATG | 23092 |
| rs199977502 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013141 | TACTAACTTTGAGTA[A/C]CAATTAAGCTAAATA | 23092 |
| rs199986817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041810 | CATCACTGTTTCTTT[C/G]CTCAGGGATCAACGA | 23092 |
| rs199991217 | in-del | -/GC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170686 | TGTACTCCACATTTT[-/GC]ACATGAGGCATAGAG | 23092 |
| rs200007427 | in-del | -/TC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795047 | GTCATATCTTCTTCT[-/TC]TTTTTTTTTAAAAAA | 23092 |
| rs200007867 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143592 | CTGTCTAAAGCACCT[G/T]AAAAATTCAGTCACG | 23092 |
| rs200010829 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909957 | CAATTATAGTGGATG[G/T]TTGGTTCTCCAGAGA | 23092 |
| rs200012377 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878560 | GTGTGTGTGTGTGTA[A/T]AAATGTGTAGTGTGT | 23092 |
| rs200028591 | snp | A/C/G/T | 0.000187327 | 0.00967658 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147409 | TCCAGCTGCCTACCC[A/C/G/T]ACAAGGGCTTTGGTC | 23092 |
| rs200035763 | in-del | -/T | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775135 | AGTAATGTATATATA[-/T]TATAAAATAAAATAG | 23092 |
| rs200072175 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087636 | TAACCCTGGCCCATT[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs200073774 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160485 | TGGTGGTTTTTTTTT[C/T]TTTCTTTTTTTTTCT | 23092 |
| rs200079730 | snp | A/G | 3.29484e-05 | 0.00405871 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932026 | ACTGGTTTCATATCC[A/G]TGTCCCTCCTTTCTC | 23092 |
| rs200093916 | in-del | -/GG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057152 | TCTTTCTAGCAGGCT[-/GG]TTGTCATATGTGACT | 23092 |
| rs200107832 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844053 | AGCTAAAAGTGAGTT[-/G]TTTTTTTTTTTTTTT | 23092 |
| rs200124078 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992068 | TAGGACTTTTTTTTG[G/T]TTTTGAATATTCCCT | 23092 |
| rs200135480 | snp | C/T | 0.000185104 | 0.00961862 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147221 | GGGACTTGTGGCTTT[C/T]CCCCCCCAGAGGAAC | 23092 |
| rs200145920 | in-del | -/GGTC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090454 | TACGATAGCTATCTC[-/GGTC]AGTCGTGTCATTAGA | 23092 |
| rs200161295 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823612 | AGCAAGTACTATAAG[-/A]AAAAAAAAAATCCTG | 23092 |
| rs200163215 | in-del | -/AT | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878543 | TGTGTGTGTGCACGC[-/AT]GTGTGTGTGTGTGTA | 23092 |
| rs200167348 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971029 | TTAAGATTCTACAAA[-/T]TTTTTAGGTGGCATT | 23092 |
| rs200170686 | in-del | -/A | 0.21695 | 0.247806 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118944 | TAAAAGTATAATAAT[-/A]AAAAAAAAAAAAGAA | 23092 |
| rs200173983 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804786 | CATGAGCCACCATGC[C/T]CGGGCTGAACAGATT | 23092 |
| rs200208993 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927027 | CTGTTCTTTAAAACA[C/T]AGGTAATAAGAGTAG | 23092 |
| rs200216351 | in-del | -/TTTT | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163462 | TTGTTTGTTTGTTTG[-/TTTT]TTTAAGATGGAGTCT | 23092 |
| rs200226118 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838032 | GAGAAGCCGAGGCAG[A/G]TGGATCACCTGAGGT | 23092 |
| rs200227467 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048785 | CAGGCGTGGTGGTGC[A/G/T]CATCTGTAGTCCCAG | 23092 |
| rs200233602 | snp | A/G | 1.65002e-05 | 0.00287225 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143057731 | ATGTTACAGCTGCTC[A/G]TGAACCACTTGGCAA | 23092 |
| rs200234292 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096685 | GCTTTTTTTTTTTTT[-/T]AATCTGTGAGTGTGT | 23092 |
| rs200244300 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207293 | CATCCACGTCCAGCG[A/T]CTCATCCCCCGTCAG | 23092 |
| rs200250795 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184348 | CCTTTTGTCTCTCCC[-/G]TAAAAACATGTATAA | 23092 |
| rs200262998 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110101 | ATGTCCTCATGGCTT[A/C]GCAAGACATGCCTTC | 23092 |
| rs200269344 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109168 | GGTAACTCGCACCTA[A/G]AAGCTCTTACCTGCT | 23092 |
| rs200276995 | snp | A/G | 1.65556e-05 | 0.00287707 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142873457 | AATTTAAATTTCAGT[A/G]CATAGGAGATGCAGA | 23092 |
| rs200277333 | snp | A/G | 1.66374e-05 | 0.00288417 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054432 | TATTGTCTTTTCTTC[A/G]TTTTAGACCCCAAGA | 23092 |
| rs200282524 | in-del | -/AC | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964544 | TTTTCTCTGTTTAAA[-/AC]ACACACACACACACA | 23092 |
| rs200313220 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905402 | AGCACTTTTTTTTTA[A/T]TTTTAAATTTTTTGT | 23092 |
| rs200325625 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228384 | ACACAAGAGAGGCTG[G/T]GGATGGCCTATTAAA | 23092 |
| rs200330930 | in-del | -/C | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849819 | CAGTCTGCTTCACCT[-/C]CCCATGCTCCCTGTT | 23092 |
| rs200335553 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948042 | GTCTTAAACAAAACA[-/T]TTTTTTTTTGAATGA | 23092 |
| rs200339143 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779450 | GTGTGTGTGTGTTTT[A/G]TTTGCCAGATAGACA | 23092 |
| rs200341917 | in-del | -/T | 0.0494327 | 0.149241 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996365 | GGGTTTGGTGGCATG[-/T]GCCTGTAATCCCAGC | 23092 |
| rs200360096 | snp | C/T | 0.316968 | 0.240864 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898191 | ACACACACACACACA[C/T]ATATATACACACACA | 23092 |
| rs200372247 | in-del | -/C | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896814 | TCTGAGCCTTACTTT[-/C]CCCATCTGCAGAATG | 23092 |
| rs200379756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932411 | TCAGCCTCCCGTAGT[A/G]ACTTACCTCCCCTTA | 23092 |
| rs200386426 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993821 | CAGCTAATTTCTTTT[C/T]CTTTTCTTTTCTTTT | 23092 |
| rs200386668 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948652 | TACTTTCCTTAGCTC[-/T]TTTTTTTTTTTAAGA | 23092 |
| rs200410845 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923099 | GGAGTTTTTTTTTTT[C/T]TTTTAATTAAATGAG | 23092 |
| rs200424836 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012756 | CCTCCTGGGTTCATG[A/C]CATTCTCCTGCCTCA | 23092 |
| rs200443349 | in-del | -/ATT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144415 | ATTATTATTATTATT[-/ATT]TTTTAAAGGAGGCAG | 23092 |
| rs200457559 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087639 | CCCTGGCCCATTCTT[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs200463971 | in-del | -/AATAGCCATAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202487 | TGAAAATAGCCATAA[-/AATAGCCATAC]TGCCCAAAGTAATTG | 23092 |
| rs200469865 | snp | A/G | 0.184521 | 0.241273 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891611 | CTAAGCTCTTAAGAT[A/G]TCAAGTAGCATATTG | 23092 |
| rs200474854 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038323 | CCTACCCTTATGTAT[A/G]CTGTCAAAAGATATT | 23092 |
| rs200480925 | in-del | -/AC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093585 | CTCTCTCTCTGCCTC[-/AC]TCTTTCTCTCTGTCT | 23092 |
| rs200481847 | in-del | -/A | 0.0244538 | 0.107838 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889581 | GAGATCATGCCACTC[-/A]CACTCCAGCCTGGGC | 23092 |
| rs200482898 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123477 | GTATAAACTCCCTGC[-/C]AATAGAACTTAACTT | 23092 |
| rs200484440 | in-del | -/C | 0.0581099 | 0.160244 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031031 | CGTCTGAGTGAGTTT[-/C]TTGAGGAAAGGACAC | 23092 |
| rs200487022 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077080 | GGCTTATATGCCTGA[C/T]AGACTTTTCATTTTG | 23092 |
| rs200488161 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795048 | TCATATCTTCTTCTT[C/T]TTTTTTTTTAAAAAA | 23092 |
| rs200489566 | in-del | -/AG | 0.0509478 | 0.151255 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985282 | TAAAAAAAATTAAAA[-/AG]GTTGTAAAGTTACAG | 23092 |
| rs200494430 | snp | A/G | | | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142913234 | CCTCAAATCCTGCAC[A/G]CGGCGGAAAACAGAC | 23092 |
| rs200504840 | snp | A/G | 0.44651 | 0.154543 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183092 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAACCTCAT | 23092 |
| rs200526144 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838352 | AGGTTTTGCATTTTT[-/C]TTCCTCCTTATAGCC | 23092 |
| rs200540106 | in-del | -/C | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964588 | AAACAACAACAGCAG[-/C]AAAAAAAACCGATGT | 23092 |
| rs200540201 | in-del | -/CT | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093586 | TCTCTCTCTGCCTCA[-/CT]CTTTCTCTCTGTCTT | 23092 |
| rs200546002 | in-del | -/GGTG | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221905 | AGTTGATACTGGGCA[-/GGTG]GGTGGGTGGATGGAT | 23092 |
| rs200548350 | snp | C/T | | | intron-variant, synonymous-codon | ARHGAP26 | GRCh38.p7 | 5:142919277 | CATGAAGGCAGAAGT[C/T]GAGGTGATGCACCTA | 23092 |
| rs200553256 | in-del | -/TTAAGTT | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009931 | TGGGTTGCTCCTGGA[-/TTAAGTT]GAGTTGAGTTCTATT | 23092 |
| rs200553413 | in-del | -/ATAAGTATGTA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035126 | AAGCATCACTAAGCA[-/ATAAGTATGTA]TGTAAGTATAGGAAC | 23092 |
| rs200555783 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889964 | ACGTGGAGAAACCCC[A/C]ATCTCTATTAAAAAT | 23092 |
| rs200564975 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053868 | ATCTTGTTTTTTTTT[-/T]ATTTGACATTATATA | 23092 |
| rs200571749 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949339 | TATGTTCCTCTCTAT[A/C]AACAGGCTCAGGACC | 23092 |
| rs200573018 | snp | C/T | 6.63119e-05 | 0.00575774 | ARHGAP26 | 5 | allele_origin=T(germline)/C(germline) | 5:143134097 | ACACCGTTCAGTCAA[C/T]AGAGAAACGTGAGTC | 23092 |
| rs200591006 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222118 | GTTTCCTTTTTCATT[A/C]TAAAGAAAGTTCAGG | 23092 |
| rs200634903 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224120 | TACTTTTTTTTTTTT[C/T]AAAAGATAAACTTGT | 23092 |
| rs200656496 | in-del | -/T | 0.305934 | 0.243663 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800369 | TTTTTTTTTTTTTTT[-/T]CTGAGATGGAGTTTC | 23092 |
| rs200678768 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160061 | GAGAAAAGATTTTTC[-/T]TTTTTTTTTTTTTTT | 23092 |
| rs200682430 | in-del | -/CT | 0.0448719 | 0.142907 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800302 | TTCCTCCCCCTCTCT[-/CT]GTCTCTGTCTGTCTC | 23092 |
| rs200686578 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954711 | AACTTGACTAGTGTC[C/T]AGTGGTGATATGACG | 23092 |
| rs200689443 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899477 | AGGCACAGGGAGGCG[A/G]GAAAGATCTTTCCTA | 23092 |
| rs200710464 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016702 | ACTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 23092 |
| rs200719618 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222284 | ACACACACACACACA[G/T]CCCACACACACATCT | 23092 |
| rs200734791 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081041 | AGGATGACTCCTGGG[A/T]TTTTGGCCTTCACTG | 23092 |
| rs200735964 | snp | C/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143121053 | TGGTGTTTGGACCCA[C/G]TCTGCTGAGGCCTCA | 23092 |
| rs200765880 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062908 | CCATCAAGACTAGTC[G/T]AAATAAAATAGCCGT | 23092 |
| rs200767347 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804800 | CCCGGGCTGAACAGA[-/T]TTTTTTTTTTAAACT | 23092 |
| rs200769179 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073546 | TTTCCCTATTGGCGG[G/T]AGGGGAGAGCATTGG | 23092 |
| rs200775661 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808167 | ATGAACCCGGGAGGC[A/G]GAGCTTGCAGCGAGC | 23092 |
| rs200782152 | snp | C/T | 1.7475e-05 | 0.00295588 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222351 | TTTCTCTCCCCTTCC[C/T]GTACAGTTCACCCAT | 23092 |
| rs200807910 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965151 | TTTCACTAATTTACT[A/G]CTGCTATCTAGAAGG | 23092 |
| rs200821551 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928262 | TTAAAACTCATTGCC[C/T]TTTCCATCTCTTGAG | 23092 |
| rs200828890 | snp | C/T | 0.00299544 | 0.0385843 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216205 | AGTGTCCTTCAGCTT[C/T]CACAGCCATCTTCAC | 23092 |
| rs200846694 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228387 | CAAGAGAGGCTGTGG[C/T]TGGCCTATTAAAATG | 23092 |
| rs200883261 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928890 | CTGATATTTACTCCA[A/T]TTTCTCTTTCATTGT | 23092 |
| rs200889210 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934766 | ATTTTTTTTTTTTTT[-/T]GGAGGGGGTTAATTT | 23092 |
| rs200893634 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168445 | TCACCATCTGGAACT[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs200898033 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937789 | AAAAAGGCCAGTCTC[-/A]AAAAAAAAATATACT | 23092 |
| rs200906174 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157175 | ACACATTCTTTCTTT[-/C]TTTTTTTTTTTTTTT | 23092 |
| rs200933202 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162299 | TACACACACACACAC[A/G]CACACACACACACGC | 23092 |
| rs200933733 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017132 | CAAATTCCAAATGTC[C/T]GGCATTTTCTTTTCT | 23092 |
| rs200948212 | snp | G/T | 0.000146962 | 0.00857083 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041931 | GCAGGTCCCTGGATG[G/T]GGGGCCCACTCTGAA | 23092 |
| rs200996861 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008657 | AGCATCTTTATTTTG[C/T]CCAGATTTTGATCCA | 23092 |
| rs200996894 | in-del | -/AAG | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973720 | TCTGTTACATACCTT[-/AAG]ACCCAGGACATTTCT | 23092 |
| rs201020052 | in-del | -/T | 0.136718 | 0.230877 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768899 | AATTTTTTGTAGAGA[-/T]TGGGGGGGGTCTCGC | 23092 |
| rs201059191 | in-del | -/GAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958924 | AAAAAAAAAAGAAAA[-/GAA]AAAAAAAGAAAGGAA | 23092 |
| rs201063901 | snp | G/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226790 | GTGCTTTTCGGTGAG[G/T]GGCAAAGAGAAAGAA | 23092 |
| rs201081628 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927330 | GCCCATATCTCTTTT[C/T]AAAAAAAAAAAAAAA | 23092 |
| rs201086238 | snp | A/C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949337 | AATATGTTCCTCTCT[A/C/G]TGAACAGGCTCAGGA | 23092 |
| rs201094846 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142492 | AACTCCTTTTTAAGA[-/T]TTTTTTTAAAAAAAA | 23092 |
| rs201095614 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840177 | TCAAGGACTGGGTAG[-/T]TTTTTGAGGTCCTTT | 23092 |
| rs201100305 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014703 | CCTGTAAGCACTCTG[-/T]GTTAATCATGATTTC | 23092 |
| rs201120807 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076914 | AGAGTTGTTTCTAAA[G/T]TTTTTAACATTATAA | 23092 |
| rs201121420 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938179 | GTATCATTGGATTAT[-/G]GGGGGGGGAAGTAGG | 23092 |
| rs201121634 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988491 | GTGTCTCTGTCTCCT[-/C]CAGTTCTGCTCTGAT | 23092 |
| rs201126086 | in-del | -/TT | 0.457688 | 0.139161 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159925 | TCTTGTGGTATGGGA[-/TT]TTTTTTTTTTTTACA | 23092 |
| rs201129917 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861363 | CCGTTTTTTTTTTTT[C/T]TTTTTTCTTCCAGAA | 23092 |
| rs201138665 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028003 | GATCCACAGCCCCCA[G/T]TTCCTTTCTGACTGT | 23092 |
| rs201140947 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803017 | TGTGTAGTGGCGGGG[C/T]GATACCCCTTAATCC | 23092 |
| rs201147802 | snp | A/G | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768904 | TTTTGTAGAGATGGG[A/G]GGGGTCTCGCTGTGT | 23092 |
| rs201149826 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221923 | GGGTGGGTGGATGGA[A/T]GGAAGGAAGGAAGGA | 23092 |
| rs201156321 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116004 | TAAAAATAGAATCGA[A/C]AGGATAAGATGGGAA | 23092 |
| rs201177393 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207231 | AACTTCACCCCTCTC[A/G]CCATCTTGGCCCATG | 23092 |
| rs201181325 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824487 | GCATCAGCAGCTGTA[C/T]AAGCTCCAGAGTGGG | 23092 |
| rs201183455 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791343 | AGCCTCCATCTCCTC[G/T]CCCATTCTTTTGCCA | 23092 |
| rs201187459 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947173 | GAGAGACCTCTCAGG[-/T]TAGAAATATGTCCTC | 23092 |
| rs201200878 | snp | A/G/T | 0.000689274 | 0.0185539 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014030 | TTCTACAGTGAACCT[A/G/T]TAGGGTGGCATAAAA | 23092 |
| rs201227111 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022568 | TACAAAACAGGCAAT[G/T]GTGAATTTGGCCCAG | 23092 |
| rs201236164 | in-del | -/AA | 0.480223 | 0.0974544 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212355 | TCCCAGCCTCTCAAG[-/AA]AAAAAAAAAAAAAAA | 23092 |
| rs201237912 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132536 | AATCATGTCTGAAGA[-/T]TTTTTTAATGAATGA | 23092 |
| rs201245059 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154174 | TTAAAAAAAAAAAAA[C/T]AGTTTCTGCTTTCAT | 23092 |
| rs201280021 | snp | A/G | 0.000844476 | 0.0205311 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207484 | TCCAGGTAAAATCTC[A/G]GATGATGACCAATCT | 23092 |
| rs201322411 | in-del | -/TTG | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865711 | TAGTAAAAGGCTTAA[-/TTG]TTGTTTAAGTTGATC | 23092 |
| rs201337868 | in-del | -/G/T/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160474 | TTGTTGCTTTTGGTG[-/G/T/TT]GTTTTTTTTTCTTTC | 23092 |
| rs201348520 | in-del | -/CC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027542 | CTTACTGGTTTTAAA[-/CC]AATTCATCCATTTTT | 23092 |
| rs201349675 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040592 | TCAAATAACAAACAT[A/T]ATTTCAGATATTGTT | 23092 |
| rs201359687 | in-del | -/TT | 0.0138799 | 0.0821421 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971573 | AGTGCTAGACTACTC[-/TT]TTCTGTACCTGCTGA | 23092 |
| rs201365123 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144798 | ACATTTGATTGGCTG[G/T]TGGTCTTATTCTCTA | 23092 |
| rs201365678 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162284 | TCCCAAACACACACA[C/T]ACACACACACACACA | 23092 |
| rs201373359 | snp | C/T | 0.455502 | 0.142369 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915370 | TTTTTTTTTTTTTTT[C/T]TTTTTTGAGATGGAG | 23092 |
| rs201379875 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011326 | TTTTTTTTTTTTTTA[A/G]TTTCTCCAATGTACT | 23092 |
| rs201415542 | snp | A/C | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964547 | TCTCTGTTTAAAACA[A/C]ACACACACACACACA | 23092 |
| rs201430334 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878557 | CATGTGTGTGTGTGT[A/G]TATAAATGTGTAGTG | 23092 |
| rs201434072 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222910 | GCACTCTCTCTACCC[G/T]ACCTCTCAGTACTTG | 23092 |
| rs201439646 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918335 | TATTTGTAGTAGAGA[C/T]GGGGTTTCACCATGT | 23092 |
| rs201442913 | in-del | -/GAT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028192 | GATGATGATGATGAT[-/GAT]AAGAAAATGATGCAC | 23092 |
| rs201452111 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100215 | ATATCAGGTTCAGTA[A/G]CACAGCCACTTCTGA | 23092 |
| rs201456622 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109169 | GTAACTCGCACCTAG[A/C]AGCTCTTACCTGCTC | 23092 |
| rs201456767 | in-del | -/C | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038779 | GGTTCACTGCAAACT[-/C]CCAACTCCCTGGTTC | 23092 |
| rs201507121 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986107 | ACAATAGTTGAACTA[A/G]TTTACAGTCCCACCA | 23092 |
| rs201519725 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949103 | AGTGAGACTCCGTCT[-/C]CAAAAAAAAAAAATT | 23092 |
| rs201520265 | in-del | -/CA | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015739 | GTGGGGGAGGAGAGG[-/CA]CGTGAATGGAGACCT | 23092 |
| rs201521472 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849922 | ACCCAGTTAGTCCCC[-/A]AACCCCACGGGTGTT | 23092 |
| rs201531042 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958922 | AAAAAAAAAAAAAGA[A/G]AAAAAAAAAGAAAGG | 23092 |
| rs201538985 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154853 | TGATAATTCATAGCA[-/T]TTTTTTTTTTAAAAA | 23092 |
| rs201553329 | snp | A/C | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115355 | AACAACAACAACAAA[A/C]AACGAAAGAAAGAAA | 23092 |
| rs201562963 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907598 | TAACATAGTTTAAGG[G/T]TAGGGTAGATGAGCA | 23092 |
| rs201573268 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891614 | AGCTCTTAAGATGTC[G/T]AGTAGCATATTGTAT | 23092 |
| rs201579740 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899261 | GGACTTCAACATATC[-/T]TTTTTTGGGGGACAC | 23092 |
| rs201581967 | in-del | -/GT | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867289 | TAAGATTTGCACAGG[-/GT]GTGTGTGTGTGTGTG | 23092 |
| rs201602856 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889965 | CGTGGAGAAACCCCC[A/T]TCTCTATTAAAAATA | 23092 |
| rs201610366 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190031 | GGACAGAAGGAGGGG[-/A]GGGGAAAAAAAAAAA | 23092 |
| rs201615670 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993822 | AGCTAATTTCTTTTT[C/T]TTTTCTTTTCTTTTC | 23092 |
| rs201615844 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947094 | TCTTTATTTTTAAAA[A/G]TAAAAAAAAAAAAAA | 23092 |
| rs201618961 | snp | G/T | 1.66181e-05 | 0.00288249 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907810 | AGGAAAAGGGGTGAG[G/T]TCATTTTTAAAATTT | 23092 |
| rs201625133 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995626 | TCAAGGATCTAGAAC[C/T]AGAAATACCATTTGA | 23092 |
| rs201638996 | snp | C/G/T | 0.000951627 | 0.0217932 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147406 | ATGTCCAGCTGCCTA[C/G/T]CCCACAAGGGCTTTG | 23092 |
| rs201646339 | in-del | -/GT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779446 | TGTGTGTGTGTGTGT[-/GT]TTTCTTTGCCAGATA | 23092 |
| rs201654888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168094 | ATTGGCACTTGAACA[C/T]GCATCTTGAGGATAG | 23092 |
| rs201674493 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115358 | AACAACAACAAAAAA[C/T]GAAAGAAAGAAAAGA | 23092 |
| rs201675780 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139674 | TAGCTTTAATATGCT[C/T]GGCCAAGCCACTCAC | 23092 |
| rs201684027 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793275 | TTTTTTTTTTTTTTT[A/T]ATCTATCTTTCTTTA | 23092 |
| rs201684453 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142932068 | GGTTATCACCATGCA[A/G]GCTTTGTCGGAAGAG | 23092 |
| rs201695533 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010094 | AGTGGGCAACTGTGA[C/T]ATCTGTAGAAGAAGG | 23092 |
| rs201699885 | in-del | -/TTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062520 | ATGTTGTAGCTTGGG[-/TTT]TTTTTTTTTTTTTTT | 23092 |
| rs201705773 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811082 | GGAGTGTTCCAGGAC[-/T]TGAGGGAAAGGAGGA | 23092 |
| rs201707577 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855884 | CTCCAGTGACTTATT[-/A]CCAGGAATGTAGGTC | 23092 |
| rs201713844 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104073 | ATAAAAGCTTTCAAA[A/G]TAGCAATACCTTATT | 23092 |
| rs201723613 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081770 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCC | 23092 |
| rs201725628 | in-del | -/ACA | 0.0158469 | 0.0875917 | utr-variant-3-prime, cds-indel, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227528 | AGCATCAAAATGACA[-/ACA]GCAGCAGAGCAGCGA | 23092 |
| rs201734653 | in-del | -/AAAAAAAAAAAAAAAAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167483 | GCAAGACTCCATCTC[-/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 23092 |
| rs201736195 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040417 | AAGATTGTGTTTTGG[-/C]CCCCAAGTATTTTAT | 23092 |
| rs201747404 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929865 | ACGAACTAGAGACAT[G/T]TTGGCTCCTTGACCT | 23092 |
| rs201751760 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904538 | AAGAAAAAAAAAAAA[C/T]AGCCAAGAATACTCA | 23092 |
| rs201760868 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073547 | TTCCCTATTGGCGGT[A/G]GGGGAGAGCATTGGC | 23092 |
| rs201764945 | in-del | -/T | 0.412917 | 0.189626 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039528 | CAACAGGAGTTTTAA[-/T]TTTTTTTTTTTAAAT | 23092 |
| rs201767068 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869189 | ACTTTCTTTTCTTTT[C/T]TTTTTCTTTTTCTTT | 23092 |
| rs201783309 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987152 | TTCTTCCATTTGTTT[C/G]TGTCCTCTTTTATTT | 23092 |
| rs201784948 | in-del | -/A | 0.0528381 | 0.153711 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111973 | TGACACACTTAGAAG[-/A]AGGTGGCCTCCCACA | 23092 |
| rs201790498 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795049 | CATATCTTCTTCTTC[-/T]TTTTTTTTAAAAAAA | 23092 |
| rs201794514 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103561 | AATGCCCATGAATGT[C/T]AGACTGGATAAAAAA | 23092 |
| rs201840915 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163532 | CTTGGCTCACTGCAA[A/C]CTTTGCCTCCTGGGT | 23092 |
| rs201840970 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061622 | TATCATTTAGGATGC[-/T]TTTGAGCTGCAAGAA | 23092 |
| rs201843296 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131187 | TTCCTGCTCTGCTGT[A/G]TATAAATATTGTCTT | 23092 |
| rs201854822 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992440 | TTTATTTTATTTTTT[-/A]TTTTTTTTTTTGAGA | 23092 |
| rs201871053 | in-del | -/TAT | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009927 | CGCTTGGGTTGCTCC[-/TAT]TGGAGAGTTGAGTTC | 23092 |
| rs201874069 | in-del | -/ATA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189583 | ATTTTTTCCATTAGG[-/ATA]ATAATTAAAATATTA | 23092 |
| rs201892178 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893291 | CCCACCCCTTTCTTA[A/G]CCTCTGATAACTCTC | 23092 |
| rs201899144 | snp | A/T | 1.67849e-05 | 0.00289692 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054403 | ATTAGTTCCATTTTA[A/T]GCTGTGCTTTATGTA | 23092 |
| rs201910531 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947120 | AAAAAAAAAAAAAAA[C/T]AGAGAGAGAGAGATG | 23092 |
| rs201921386 | snp | C/T | 0.00199804 | 0.0315441 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143214074 | CGTTCACAGCAGGCA[C/T]GGTCTTCGATAACGG | 23092 |
| rs201923814 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888284 | AGTTTGCTTTTCTAC[A/G]TCTCTATCTGGGGAG | 23092 |
| rs201933685 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774269 | ATTTTTATAGTTTTT[-/A]TATAACATTGGCTGA | 23092 |
| rs201946550 | snp | A/C | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867328 | GTGTGTGTGTGTGTG[A/C]TTTGTTTGTTTTTGC | 23092 |
| rs201947939 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095664 | ACCTCCACCTCCCAG[-/C]TGGGTTCAAGCAGTT | 23092 |
| rs201952842 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092157 | TTGCAAACATCCCTT[A/T]GTTTTTTTTTTTGTT | 23092 |
| rs201984479 | snp | A/G | | | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069796 | CTTGTAAGTGCCTCA[A/G]TAGCCCTATTATGCA | 23092 |
| rs202002212 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937799 | AGTCTCAAAAAAAAA[A/T]ATACTTTAATTTTGT | 23092 |
| rs202006357 | snp | A/G | 0.00230261 | 0.0338527 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770945 | CCCCTCGGGGACGCG[A/G]CTCCGGGGCGGGAGG | 23092 |
| rs202012760 | in-del | -/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212859 | TTTTAAAATACTGAT[-/G]GCCTGGCCGGGCGCG | 23092 |
| rs202020916 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228280 | CACATATTTACATCT[C/T]TGAAGACATAGACAC | 23092 |
| rs202023068 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210234 | AGGAGGAGGAAGTCA[C/T]GTCTTTCATGGATGG | 23092 |
| rs202030563 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785604 | ATTTCTACAGAGGAA[C/T]AAAATTGCCAGTACT | 23092 |
| rs202043712 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116419 | ATTTTTCAACATAAC[-/A]ACTCTAGGCCTCAAG | 23092 |
| rs202061609 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936836 | GGAAAAAAAAAAAAA[-/A]GCCTTGACTTAAACC | 23092 |
| rs202069448 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989244 | CCTTTACCATTATGT[A/C]ATGGCCTTCTTTGTC | 23092 |
| rs202078962 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881396 | CAGTGATCTTAATGA[C/T]AGGAGGAGCTACTGT | 23092 |
| rs202085441 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945623 | TATCAGAGGCTTGGT[-/TG]TGTGTGTGTGTTTGC | 23092 |
| rs202086461 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866042 | TCTTTTTTCTTTTTT[C/T]TTTTTTGGAAGCCCC | 23092 |
| rs202088562 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204847 | TTTTAATTGTCCTGT[-/G]GTAACCACTGACCAA | 23092 |
| rs202098776 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778805 | GTCCTTTGCATCCTT[A/G]TAGCCGGTTGATAAT | 23092 |
| rs202100045 | in-del | -/AT/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937798 | AGTCTCAAAAAAAAA[-/AT/T]TATACTTTAATTTTG | 23092 |
| rs202108989 | snp | A/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143056083 | AGTTTCATCAAAGCA[A/G]CAAGTAAGTCTTTTT | 23092 |
| rs202112689 | in-del | -/TG | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977597 | CTTTGCGTTGAACTC[-/TG]AGCAGTTTCCTGGGT | 23092 |
| rs202118502 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087569 | TGCTCTCCTCCTCTG[A/T]CCCTAGGGCTTTTGT | 23092 |
| rs202122548 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992662 | TCGATCTCCTGACCT[C/T]GTGATCCGCCTGCCT | 23092 |
| rs202123956 | in-del | -/TA | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079369 | GTTTCCAGCGTCCTC[-/TA]TGTGTCTATAAACAC | 23092 |
| rs202130914 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213124 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 23092 |
| rs202135111 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076911 | CTTAGAGTTGTTTCT[A/T]AAGTTTTTAACATTA | 23092 |
| rs202137519 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162288 | AAACACACACATACA[A/C]ACACACACACACACA | 23092 |
| rs202142526 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905400 | ACAGCACTTTTTTTT[A/T]AATTTTAAATTTTTT | 23092 |
| rs202143647 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162990 | AGTGTGGTGGTATGC[A/G]CCTGTGGTCCCATCT | 23092 |
| rs202149901 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947095 | CTTTATTTTTAAAAG[A/T]AAAAAAAAAAAAAAA | 23092 |
| rs202150051 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048748 | GTGAAACCCCATCTC[C/T]ACTAAAAATACAAAA | 23092 |
| rs202169547 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897051 | TATTTATTGAATACC[A/G]TAGAAAATGCTGAAA | 23092 |
| rs202170232 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946079 | GTTGTCACTATCCTC[C/T]CTTCATCTAGGTAAT | 23092 |
| rs202196051 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775638 | ACAATAACTCCCCAC[-/T]TTCCCCTCCCCCAAC | 23092 |
| rs202196836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185414 | CTTTCTGTATTAAGA[A/C]AAAATTTCTGCATTA | 23092 |
| rs202197507 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837578 | CCTTGTGCCCTGTAC[A/T]TGCCCTTTGGTACTT | 23092 |
| rs202198182 | in-del | -/TGCA | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770465 | CGGGGAGGCGGCGTC[-/TGCA]CTCGCTCGCCCGCTC | 23092 |
| rs202198649 | in-del | -/TA | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873801 | CCCCTTCAACCATAG[-/TA]TACTAAGAGCTTAGA | 23092 |
| rs202204031 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059662 | CTTGACACATTTTTG[-/T]TTTTTTTGGCCTTCT | 23092 |
| rs202210306 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222443 | TTACGTGGAGTTCCT[C/T]TAACCGTGGGCCCCA | 23092 |
| rs202221430 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154160 | GTGATTTAAAAATAT[A/T]AAAAAAAAAAAAAGA | 23092 |
| rs202225536 | in-del | -/CTTTCCCTTTCC | 0.431325 | 0.172108 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951001 | CCTCTTTCCCTTTCT[-/CTTTCCCTTTCC]CTTTCCCTTTCTCTT | 23092 |
| rs207466436 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092265 | GCCTCCCAGGTTCAC[G/T]CCATTCTCCTGCCTC | 23092 |
| rs367551639 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205071 | AACTGTGGAAGAAAA[C/T]GGAGACTGCACAGTA | 23092 |
| rs367556202 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819987 | TTTGGATTTACTTAC[C/T]GGTCTGCCGTTGTTT | 23092 |
| rs367564227 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114809 | GGGATTGACCGTGAC[C/G]TATCTCTTAGAGGAA | 23092 |
| rs367571479 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171532 | GGGGAGAGGAATAAA[A/G]TTTTATGGGACACCT | 23092 |
| rs367581755 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139244 | CTCTACTTATGTGCC[C/T]ACTAACCTCATTATC | 23092 |
| rs367586056 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890202 | TATATATATATGAAA[A/G]TGCATTGCATTTAAC | 23092 |
| rs367589926 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867029 | GGAAGCCAGGGCCCC[C/T]CTCTCAGTTGCTGAG | 23092 |
| rs367589982 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108320 | GTAATTTTCATGGAT[A/G]TTAGAGCTCTAGGAT | 23092 |
| rs367592274 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900770 | AATGTTTAACAGGTT[-/A]AAAAAAAATCATTTA | 23092 |
| rs367594184 | snp | A/C/T | | | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229167 | TGAGAAGCTTTGCTT[A/C/T]CCATTTAGGAAGAGG | 23092 |
| rs367595252 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909980 | TCCAGAGACTTCAGA[A/G]AGTTACTAGAAAGCA | 23092 |
| rs367604154 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097310 | AGATTGTACCACTGT[A/G]CTCTGCACTCCAGCC | 23092 |
| rs367606143 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930035 | CAAGTTCCCAGGCAC[A/G]GCCCAGTTCAGATTG | 23092 |
| rs367606442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871955 | AGCTATCTCGGGACC[A/G]TGTCATCACAGCGTG | 23092 |
| rs367608593 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858723 | GGAGCTGTTCACATT[A/G]AACAGTCACCACACT | 23092 |
| rs367609450 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779426 | CTGGGGTTAGGGTGG[G/T]GTGTGTGTGTGTGTG | 23092 |
| rs367610962 | in-del | -/CACA | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174405 | AGGGGAGTGTGAAAT[-/CACA]CACACACACACATCC | 23092 |
| rs367615780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914282 | TCCCATGGAGACAGC[A/G]TGCCCCCTTAGCCTT | 23092 |
| rs367622638 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872595 | GATGTTGAAGACTCC[A/G]GAAGGATCACTGGCT | 23092 |
| rs367633418 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970423 | ACTCTTTCTGTTTTC[C/T]TCTCTGTTGGCTTCA | 23092 |
| rs367634682 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890369 | AGCGGTTTGGAGTGT[A/T]AGAGGACAGGAAGGA | 23092 |
| rs367643138 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993271 | GCTTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 23092 |
| rs367644661 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958197 | TGGTTTGGCACCCAG[A/T]TTGTGTTTTAAACAA | 23092 |
| rs367647862 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900623 | GGGAGGGGGGGCGGG[A/T]TGAGATTCCTTTACC | 23092 |
| rs367648090 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952201 | ATTCACAGATTCTGG[A/G]GGTGAGGACATGGAC | 23092 |
| rs367653037 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032231 | GCATTCATGATGAGA[C/T]AACTGTTTGGGCTGC | 23092 |
| rs367658152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979161 | ATAATACCATGGTGA[A/G]GATGAAAAAAACGTT | 23092 |
| rs367666890 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207181 | CTGACAAGTTTTCTG[C/G]TTGTTATGTCTTGCA | 23092 |
| rs367668639 | snp | A/C | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009411 | GAGTTCCTGTCTGGA[A/C]TCTGCCCATTTCCAG | 23092 |
| rs367676795 | snp | A/G | 0.000103564 | 0.00719524 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885258 | TTTTATTCCTGCAAC[A/G]TGTTACTCTTTTTCT | 23092 |
| rs367681087 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068120 | CAGTGAGCCAAGACC[A/G]TGCCACTACACTTCA | 23092 |
| rs367685562 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041565 | AGAGAAAGGAAAGCT[G/T]CTTTCGCCGCTGATG | 23092 |
| rs367692345 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857438 | TCTCTGCTGAGGGCT[A/C]CTGGGTACAAGGTTC | 23092 |
| rs367695000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093263 | AGCAAAGCAGTTGCC[A/G]CTACAGGTTGAATGC | 23092 |
| rs367698784 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059634 | AACTGGAATTTGCAA[A/C]TCACAGTTGTGACCT | 23092 |
| rs367715687 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035959 | AAAAAAAAAAAAAAA[-/G]AAGAACTTACCCATG | 23092 |
| rs367722777 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094310 | TCGTTGCCACAGTAT[A/G]TGAGGATCCTTTAAG | 23092 |
| rs367736115 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789789 | ACAACAGCACAAGAC[A/G/T]CTCCAAAACATATCT | 23092 |
| rs367738404 | snp | A/G | 0.000115311 | 0.00759224 | intron-variant, missense, synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207397 | GTGTTCAGCCTCCTC[A/G]TCAACTTTGTTCCCT | 23092 |
| rs367742469 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821945 | GACATGAGCTGTTAG[A/G]TTGGCCATAAAGGGC | 23092 |
| rs367755397 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178743 | GGCTGTTCATACTTC[A/G]TTTTTCAAGTGGGAA | 23092 |
| rs367776188 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191371 | TTCATTCATTAAATT[-/T]GGCTCTTCCAAATAA | 23092 |
| rs367780662 | in-del | G/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893942 | GGTATTATTTGTGGG[G/TT]TTTTTTTTTTCTGTT | 23092 |
| rs367781243 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215940 | GGTTTTTGTGAGGGC[A/G]TAGGTTTCCAGTTCT | 23092 |
| rs367794102 | snp | C/T | 0.000116939 | 0.00764563 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143133978 | GCAGATATTTAACAC[C/T]GTGCCCGATATGCCT | 23092 |
| rs367794680 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008037 | AGGCTTTTTGTTTTG[-/T]TTTTTTTAAACACAA | 23092 |
| rs367832960 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799885 | CTGTTAGAGTGGCAA[A/C]TACATTTCAAACATG | 23092 |
| rs367843659 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904984 | GGGGCAGTAGTGGTG[A/T]TGGAGTATTGGCTGT | 23092 |
| rs367850308 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976867 | GTAGGTTCTCCTCAT[C/T]GTGTCAAAGATAGGC | 23092 |
| rs367882435 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997544 | CTCCCAGGTAGCTGG[G/T]ACTACAGGTGCATGC | 23092 |
| rs367915031 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793252 | GTTATATCCCTTTGC[-/T]TTTTTTTTTTTTTTT | 23092 |
| rs367916651 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001545 | TGTTTACTGTCTCTT[C/T]TTTCATCTTTTCTGT | 23092 |
| rs367937914 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187171 | GAAAATGAGGGACAC[A/G]GAGGTTAAGTTGCCC | 23092 |
| rs367947290 | in-del | -/AC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955096 | TAGTGAGACCTGTCT[-/AC]ACACACACACACACA | 23092 |
| rs367959360 | in-del | -/AGGAAGGA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221943 | GGAAGGAAGGAAGGA[-/AGGAAGGA]TGGAAGGATGGATAC | 23092 |
| rs367962984 | in-del | -/TTA | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900644 | TTCCTTTACCGTCAC[-/TTA]TTATAGCTGCCTCTC | 23092 |
| rs367966356 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093318 | GGTTAAAGATTTTTG[A/G]TAGGAAGGCTACTGG | 23092 |
| rs367980350 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778066 | AGGGTGACAGCATCA[C/T]AGATGGTGGTCAGAG | 23092 |
| rs367984190 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134840 | CATAGGAAGTTATGC[A/G]AATTAAATGAAATTA | 23092 |
| rs367990747 | snp | C/G | 5.00705e-05 | 0.00500327 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037302 | GTTCTCATAGAAGGT[C/G]ACGCATCTGGTGAGG | 23092 |
| rs367991630 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847151 | GATAACAGTGCCTGT[C/T]TCATGGGATTTTGAG | 23092 |
| rs368015908 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905846 | CAAATTTAACATTGG[C/T]GCAATATTTAATCTG | 23092 |
| rs368039637 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869121 | TTAGGCAGCCATGAG[A/G]CCAATCCTGTTGCAA | 23092 |
| rs368060892 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823678 | TTGAAAAGTATTTTT[A/G]TTTTTTAGATTTTGC | 23092 |
| rs368069584 | in-del | -/TC | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108531 | CAGTCACTTTGGTAG[-/TC]ACTGGCCCTTGAAAT | 23092 |
| rs368079758 | in-del | -/T/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076159 | ACCAGACCTGGCTAA[-/T/TT]TTTTTTTTTTTTTTT | 23092 |
| rs368081239 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036893 | GTACCTGTCACCTTA[C/T]GCTGCAGTTTCTTCA | 23092 |
| rs368085889 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926804 | TGCCCTTCTGCAGCC[A/G]TAATTTTAACCTTAC | 23092 |
| rs368089536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854833 | GCTTTGTAGGAGGTT[A/G]AATGTTGATGTTGGG | 23092 |
| rs368093566 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026600 | ATATCAGGAAGAACA[A/G]TGGTGCCCGGATGGG | 23092 |
| rs368095047 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838274 | AAGAAAAAAAAAAAA[-/A]GTTAAGGGTAAAATA | 23092 |
| rs368099127 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135344 | AGGAGCAGAGTCAGT[C/G]CTCAGTAAATGCTGG | 23092 |
| rs368101575 | in-del | -/CAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115351 | AAACAACAACAACAA[-/CAA]AAAACGAAAGAAAGA | 23092 |
| rs368107155 | in-del | -/TAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107155 | CATAGGTGTTCAGTC[-/TAC]GGTATTGGGTGTGAG | 23092 |
| rs368108270 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064143 | CACTGACAATTGGCT[A/G]GAGCTGAGTAGAAGC | 23092 |
| rs368114407 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160129 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAAGCTC | 23092 |
| rs368118338 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045872 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 23092 |
| rs368118567 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106123 | ACTTAATGATTACTT[A/T]GCTCTTTATATAATC | 23092 |
| rs368120132 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990407 | GGTTCGAGCATCCTC[C/G]TTTAACTCAGAGAAG | 23092 |
| rs368122178 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808977 | GGCACCTTGCCCATC[A/G]GATGGCTGCCCCTTT | 23092 |
| rs368129312 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898996 | AACCTGCAGTGAAAG[G/T]TGACTTCCTTTCCTC | 23092 |
| rs368133303 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935339 | ACATGGGTCAGTAAC[A/C]TTTTTCTGTAATGGG | 23092 |
| rs368136971 | in-del | -/GTTT | 0.195449 | 0.243976 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163433 | TAGAAGGAGTTCTAG[-/GTTT]GTTTGTTTGTTTGTT | 23092 |
| rs368138241 | snp | A/G | 1.7896e-05 | 0.00299126 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894188 | TGCTTTCGGAATGCT[A/G]TCCTTGGGTAGTGAC | 23092 |
| rs368142614 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210911 | GTTGACAGGAGCAGC[C/T]GAAAACTACCCCAGG | 23092 |
| rs368143392 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798953 | ATTTGAGTGGTAACC[C/T]TGAAGGCCCAGTAGC | 23092 |
| rs368149858 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182302 | AACAGTTGCAAAACT[C/T]ATCCACAGTTCATCA | 23092 |
| rs368155696 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842716 | ACATTTCTGAGGCCA[A/G]TTTCCCATTTGTAAA | 23092 |
| rs368161527 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110509 | TTGTGTGGTTGAAGG[A/G]AATGTCAGTAACAAC | 23092 |
| rs368162849 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225083 | TGAGGACAAGAAGAC[C/T]TTGGGAAATGGAGGC | 23092 |
| rs368171155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110039 | CCAGGTACTTACCCC[A/G]AGGTGTTTGTACCTG | 23092 |
| rs368174713 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086265 | TTCCAGTCCCCTCTG[A/G]CATTACTAAAATGAC | 23092 |
| rs368192321 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791535 | GTGTTTCCTAATCTT[A/C]ACACCTAGAAGAAAT | 23092 |
| rs368199224 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172738 | TGTTTGCTGGTGATC[A/G]GCCTGGTAACAGAAT | 23092 |
| rs368201907 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853271 | CTCACTGCAACCTCC[A/G]CCTCCTGGGCTCAAG | 23092 |
| rs368203796 | in-del | -/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016758 | ATTTAAATAGGAATT[-/G]TTTTTTTAGGGTATT | 23092 |
| rs368207983 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112483 | TGTAAAATACATATA[A/G]TGTAAACTTTACTAC | 23092 |
| rs368214733 | snp | A/C | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964571 | ACACACACACACACA[A/C]AAAACAACAACAGCA | 23092 |
| rs368217572 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104046 | AAAAAAAGAGAGAAA[-/T]TGAAACTTAAGATAA | 23092 |
| rs368232468 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956519 | GAGTTCGAGGCTGCA[A/G]CGAGCTATGATTGCA | 23092 |
| rs368236332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824323 | CCCCAAGAGCTAAGC[A/G]TGGAGTAGGAAGCAT | 23092 |
| rs368239057 | in-del | AA/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116002 | GATAAAAATAGAATC[AA/G]ACAGGATAAGATGGG | 23092 |
| rs368241153 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005281 | TGTTTGACCTTTTCT[C/G]CTCAAGGCTTTGCCT | 23092 |
| rs368248918 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973201 | TGGTGGAAAAGCTAA[A/G]ATAGATAGAAGAGAT | 23092 |
| rs368251763 | snp | C/T | 3.30918e-05 | 0.00406753 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142903656 | GGAGGGATACCTCTA[C/T]GTGCAGGAGAAACGT | 23092 |
| rs368256655 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996122 | GTGCAGCAAACCGAC[A/G]TGGCACATGTATACC | 23092 |
| rs368288946 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077628 | CTTAAGCAGGTCACC[A/G]TGGCTATGGGGTGCC | 23092 |
| rs368291138 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090155 | CCTTGGGGGCTGACC[C/T]GCAGGGTGCCGGACT | 23092 |
| rs368293725 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920600 | AGCTGACTCTCACCA[A/G]TGTCCATACATTTGA | 23092 |
| rs368300699 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052841 | GCTGAAAGGCTGTTG[C/G]TCCTGCAGGAGGAAC | 23092 |
| rs368338466 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095894 | TTCTTCTTCACTCAA[A/T]CTATTGTCATACAAA | 23092 |
| rs368343158 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084556 | GAGCCCTGCCCTTTT[C/T]ACTGCCCTACTTACA | 23092 |
| rs368347548 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837741 | GTTTATGAGATTCTG[G/T]ATCGTCAGCCTTGGT | 23092 |
| rs368353987 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075093 | AGCCTAAAGCTGCAT[A/G]TTTTCTGTGCTGGTT | 23092 |
| rs368367707 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820400 | TTCCCTGATCAGTCA[C/T]TTTGTGGTTGGGTTT | 23092 |
| rs368369824 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064046 | GTGGTGGTGGTATCC[C/T]ACACATTACTGTTTT | 23092 |
| rs368379627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981379 | AAGCAACTTGGGCCA[C/T]ATGAACAGAGCATTA | 23092 |
| rs368406498 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773076 | AACTACTACTTGATC[A/G]GGTCAGGTGACCTCT | 23092 |
| rs368409442 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794493 | GCATGGTTGTTACCC[A/C]CATTTGAAAATTACT | 23092 |
| rs368426863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054759 | GAAACTTTGTTCTAT[A/G]TGAGAAGTATTGTGA | 23092 |
| rs368428697 | in-del | -/C | 0.487746 | 0.0773096 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964545 | TTTCTCTGTTTAAAA[-/C]ACACACACACACACA | 23092 |
| rs368434048 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019928 | CAGATTCCATAGGTT[A/C]ATCGGGTTATGTTGA | 23092 |
| rs368442943 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126622 | GAGGTTAGAGAGAGA[G/T]TCTTAATTTGTTTCT | 23092 |
| rs368446260 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089487 | AATGCCTTTGTTATA[C/T]TTCCATCAGGGGTGG | 23092 |
| rs368486551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120480 | CTTTACATCTAAAGT[A/G]CTGAATTTCCTTACT | 23092 |
| rs368491841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044556 | TGGCCTGGATCCTGT[A/G]CGTATGTTGGGGGAT | 23092 |
| rs368495763 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928231 | TTTTTGTGTGTGTGT[-/G]TTTTTTTTTTTTTTT | 23092 |
| rs368505956 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148288 | AGATGCTAGGATGTC[A/G/T]GTAACCTTTTCCTGC | 23092 |
| rs368507783 | in-del | -/GATT/GTTT/GTTTGTTT | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163432 | TAGAAGGAGTTCTAG[-/GATT/GTTT/GTTTGTTT]GTTTGTTTGTTTGTT | 23092 |
| rs368520853 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100398 | AGCGAAGGAACATCC[A/T]GTCACTAGCCTTATC | 23092 |
| rs368522841 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032279 | CAGAGCTGAACCTGA[-/G]GCTGAGGGAGGGAAG | 23092 |
| rs368528114 | snp | A/G | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142879414 | TCACTCCCTTGGAGA[A/G]GTTTCGAAAGGAACA | 23092 |
| rs368529816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810830 | AAATAGTAAGTAACC[A/G]TAAGCGTTGATATGT | 23092 |
| rs368530298 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973996 | GGGCAGTGCCCTAAC[A/G]TTTTTAGCTTTTGCC | 23092 |
| rs368554411 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094937 | GAGGAAGTTAAGTTT[A/G]AAAGTAGAAGGCAAA | 23092 |
| rs368583515 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016476 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACAAGGT | 23092 |
| rs368591148 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223315 | GGGTGGTCTACTTGA[A/G]GCAGATGGGATAGTA | 23092 |
| rs368596969 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787030 | CTCTTAGTCGGACTG[C/T]GAGTGGTCTCATCTA | 23092 |
| rs368605514 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871954 | CAGCTATCTCGGGAC[C/T]GTGTCATCACAGCGT | 23092 |
| rs368608251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881771 | GCAGTCTCAAGAACA[C/T]CTCAGAGCCAGCAAG | 23092 |
| rs368608740 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059098 | CAACCTAGAGTCAGG[C/T]GTTTGTTAAGCAGAG | 23092 |
| rs368614100 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793986 | AGAACCAATCCAAGC[G/T]GCTTAAACAGAAAGG | 23092 |
| rs368614188 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777497 | TTTCTAAAAATTAGC[C/T]AGTGGAGGAATACTA | 23092 |
| rs368620083 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123561 | TTACTCTTTAAAATC[C/T]ACAATGTTGGCCAGG | 23092 |
| rs368623320 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857554 | CTGCAGCAAGGGAAG[C/G]ATGTCAGGGTTTCTT | 23092 |
| rs368629386 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788173 | GCCCAGCTTATTTTT[C/G]TATTTTTAGTAGAGA | 23092 |
| rs368631485 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143041824 | TCCTCAGGGATCAAC[A/G]AGCAAGGGCTGTATC | 23092 |
| rs368634142 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912305 | GTGAAAAAAGCCAGA[-/C]AAAAAGAGCACATAC | 23092 |
| rs368635302 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972560 | GTGTGTTTAAGGCAT[A/G]CAACATGATTGTAAG | 23092 |
| rs368638249 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848496 | GGTCAGATTCTCACC[A/G]TAGGTGGTTCTCCAG | 23092 |
| rs368684433 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962100 | GAGAAATGCGAGTGG[C/T]GAAAAAATGGACGAT | 23092 |
| rs368692221 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990903 | CCAGTTAGGCTACTC[G/T]GGGGTCAGGGACCCA | 23092 |
| rs368707766 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120980 | CCTTTTCTTTTCCTT[C/T]CTCCCAGTGTTGCTA | 23092 |
| rs368722882 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174415 | TGAAATCACACACAC[A/T]CATCCACCCACACCA | 23092 |
| rs368775422 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002693 | CTGCCTTTAAAAATT[G/T]CCTGAAACACTTTTC | 23092 |
| rs368782581 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149006 | GTGTGTACAAAGAGG[C/T]TGCTTAAGCAGCTAA | 23092 |
| rs368786518 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969752 | GCTTAGAGAAGTGCA[C/T]ATGGGTGGTCAGTGT | 23092 |
| rs368790228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178160 | GCATGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 23092 |
| rs368796068 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994601 | GTTGGGACTGAAGAG[A/G]AAGATACAATCATGC | 23092 |
| rs368796219 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981107 | TGATTATGAACATCA[A/G]AAGTCATCATGGAAA | 23092 |
| rs368803528 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070537 | AGACACCCCATGCTC[A/G]TGGATCAGAAAAATT | 23092 |
| rs368804344 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167375 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGACATG | 23092 |
| rs368809203 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115117 | GCAGGTGGATCACCT[A/G]AGGTCAGGAGTTCGA | 23092 |
| rs368822956 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910608 | GCCGGGTGCAGTGGC[A/G]CATGCCTGTAATCCC | 23092 |
| rs368828617 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134697 | TCACATCCGTTTTTC[A/G]TCTCAGGATTTCTGA | 23092 |
| rs368830729 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803567 | TGTTGAGAAATAAGC[C/T]GGACGGAAATCTCTG | 23092 |
| rs368837666 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821190 | GACCAAGAGAAGAGC[A/G]GGTGAATTACTCACA | 23092 |
| rs368837809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849820 | CAGTCTGCTTCACCT[C/T]CCATGCTCCCTGTTT | 23092 |
| rs368839837 | in-del | -/G | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768908 | GTAGAGATGGGGGGG[-/G]TCTCGCTGTGTTGCC | 23092 |
| rs368839966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836560 | ATAGTTTTCCTTGGC[A/G]TCACTGAGTATTTTG | 23092 |
| rs368843861 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838943 | TGCCATCATGACTTA[C/T]TTGGTCTAGATATGT | 23092 |
| rs368857461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844154 | CTTCTGGGTTTGAGC[A/G]ATTCTCATGCCTCAG | 23092 |
| rs368863628 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940811 | GCCAGGTGCGGTGGC[C/T]CATGCCTGTAATCCC | 23092 |
| rs368863738 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880047 | TATTACCCATTGTGC[-/A]AGGTCAAAAAATGAC | 23092 |
| rs368865014 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780284 | ATTATTTCCAACCTT[C/T]CACCATTGCAAGTAA | 23092 |
| rs368867918 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802218 | ATGTGTGGAAGTTGA[C/T]GTTTTTCAGATTTCG | 23092 |
| rs368870465 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775134 | ATAGTAATGTATATA[C/T]ATATAAAATAAAATA | 23092 |
| rs368872168 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900016 | ACCTTGGAATTAACT[G/T]CTTATCTTCTGCGTT | 23092 |
| rs368889365 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918187 | AGTCTTGCTCTGTCA[C/T]CCAGGCTGGAGTGCA | 23092 |
| rs368893652 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900439 | GGGGATAGATGGGCC[A/G]GGGACAGTGGCAATG | 23092 |
| rs368897097 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158101 | ATTATTTTTATTCCT[C/T]CTTCTTATTTGCTCT | 23092 |
| rs368903718 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936975 | TTTTTAGATGCAATG[C/G/T]GGAAAGCATACACAA | 23092 |
| rs368914434 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813612 | CAGGGCTGTTTTCTT[C/T]CCAGGTCTCTCTTTT | 23092 |
| rs368949568 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930094 | ATGTTAAGGGAATGT[C/T]TGATTCTGAAGCAGG | 23092 |
| rs368950888 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874048 | TTGGCTGAGCTATGC[C/G]TCTGCCACTGCCTTC | 23092 |
| rs368962769 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816639 | TGTGAAGTGCAGTGT[A/G]GCTTCAGGGAATGGG | 23092 |
| rs368975085 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168714 | CTTGGAGTTAGGCTA[A/T]ATCTCTAGGAGATTA | 23092 |
| rs368979620 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907454 | TATTTTAAGACCCAC[G/T]GGATGTAGCATCAAT | 23092 |
| rs368988547 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124800 | TGTGTGCACACAGGC[A/G]TGGGAGGATTGTTGA | 23092 |
| rs368994438 | snp | A/T | | | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194444 | TGTAATCATCAGATT[A/T]GAATTTCGAAATGTT | 23092 |
| rs368998835 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894375 | TTCAGGGTTTAATGA[C/T]GTACCCATATATTCA | 23092 |
| rs369001417 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913516 | CATTAGAACCTCCCT[A/G]TCTTTTGGGTTCAGC | 23092 |
| rs369006848 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786377 | TCATAGCTCACTGCA[A/G]CCTCGGACTCCTGGA | 23092 |
| rs369018571 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823468 | TTCCCACTTCTCCCA[C/T]TGTCCACCCTAAAGC | 23092 |
| rs369028969 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131040 | AGGGAACTGACCCTT[C/G]GGACTATGGCTCTTG | 23092 |
| rs369031052 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896008 | TAACTTCCAGCAGTG[-/TG]GTTTCAGTCAAGGTC | 23092 |
| rs369034355 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777200 | TTTCCATGTGCTTCA[A/G]CCTTAGATGTATTTA | 23092 |
| rs369065706 | snp | C/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932251 | AGTGTACCAGAGGTG[C/G/T]TTTTTTATTCCTAGG | 23092 |
| rs369073481 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770391 | CAGACACCGGCGGGG[C/T]GGCCGAGGCTGCTGT | 23092 |
| rs369079799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801522 | AACATAAAAACCCCA[A/G]TCATCTTTTTGAGAA | 23092 |
| rs369089868 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979564 | GGGGCCACATTATCA[A/G]TCCCTGCAGAAGAAA | 23092 |
| rs369092708 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937404 | AAAATACTGAATGCC[A/G]GCAAGGATGCAGAGA | 23092 |
| rs369094483 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918482 | AATACATTTCTAGAA[A/G]TCTACTTTTAATTCT | 23092 |
| rs369101783 | in-del | -/AAAAA | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100235 | GCCACTTCTGAAAAG[-/AAAAA]TAAAGGTAAATAAGT | 23092 |
| rs369108889 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892826 | CTTTGTGTTGGGAAC[A/G]TTTCATATCTTCTAG | 23092 |
| rs369114338 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222240 | TCATTGTCCAAGCTT[A/C]CTTCATACACACACA | 23092 |
| rs369114644 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134162 | TCCCATGCTACCTGC[-/A]ACGGCTCAGGGTGGA | 23092 |
| rs369116006 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117452 | TAGCTGTACCAAGTT[A/G]TGAGCAGTAATAATC | 23092 |
| rs369125200 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042079 | GGAAAGGTTCTGAGT[A/G]GGACTGGACAAAATA | 23092 |
| rs369127891 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034782 | AAAAAAAATTCCTCC[C/G]CTGGATTCCAACAGG | 23092 |
| rs369155995 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800545 | TTTTTGTATTTTTAG[C/T]AGAGTCGGGGTTTCA | 23092 |
| rs369160343 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806672 | TGGACGACATCACAG[G/T]GAAAGATTAGTGCAA | 23092 |
| rs369181467 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035413 | TGAGACTGGAGACTA[C/T]TATTCTAAGTGAAGT | 23092 |
| rs369185941 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149322 | GTCGCTGATTGATAC[C/G]TTTGGGTCTTGAGGT | 23092 |
| rs369188038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094043 | CCCACCTCCTCATGG[C/G]GACTTCTCACCTCTT | 23092 |
| rs369190074 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153026 | TGAGTTTGTGACCGC[A/G]GAGTCATGGGCAGCT | 23092 |
| rs369199850 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071572 | ATTTTTCTGGGAAAA[C/G/T]ATTTTATGAATAAGA | 23092 |
| rs369251054 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008445 | TGGTGTAGAACCAGC[C/G/T]TGTTGTTTTAAGATG | 23092 |
| rs369262311 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097945 | TATTTTGTATTGGTT[A/G]TAAAAGTCTGGAGGT | 23092 |
| rs369267236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846292 | CATGGCTGGAGTTGT[A/G]TCCAAGCTCAGAGGG | 23092 |
| rs369272308 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192132 | AGAGGGATAAGACAA[C/T]TGCAATTCAATGTAG | 23092 |
| rs369277083 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938055 | TACATACACACAGAT[A/G]AACTCATGTCAAAAC | 23092 |
| rs369282524 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918508 | ATTCTTATATATCTA[A/C]GTTGTTTTACCTTTG | 23092 |
| rs369306277 | snp | C/T | 9.88973e-05 | 0.00703128 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142907748 | TACTGTACATATCAA[C/T]GGGATTCCAAACAAA | 23092 |
| rs369323726 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790398 | ATTTCTCCTGTTTTT[A/G]TAGGCAGAATGATAT | 23092 |
| rs369327399 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169224 | GACAGTTCTATTCAA[A/G]ACCCTGTATGTCAGC | 23092 |
| rs369333936 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988939 | TTTGGAATAAGTGTC[A/G]TCTGGTGCTGAGAAG | 23092 |
| rs369334849 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901900 | CCTCTTTTCAACCTG[A/G]TTATGTGACCTTTGC | 23092 |
| rs369337454 | in-del | -/AT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823726 | CTGTCTTACTGAAAT[-/AT]GAATGTCACGGTGTG | 23092 |
| rs369338423 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089965 | GTTATTCGGCAGAGT[C/G]TCCAGTAAAGGTCCA | 23092 |
| rs369356204 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081400 | ACTCTGGAAGACTAA[A/G]CACGCTGTTTGGGGA | 23092 |
| rs369357569 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017287 | GCATACGGTGCCTGT[C/G]GAGTATAAGACAGGG | 23092 |
| rs369359202 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844051 | TGAGCTAAAAGTGAG[-/T]TTTTTTTTTTTTTTT | 23092 |
| rs369361475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113204 | TATATGCAAAGAGGT[A/G]TCTTGTCTTTTTTTA | 23092 |
| rs369377056 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928232 | TTTTGTGTGTGTGTG[-/T]TTTTTTTTTTTTTTT | 23092 |
| rs369380526 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831694 | AGCCCCCACCCTCTG[C/T]CACCCATCCCTGGGT | 23092 |
| rs369388087 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142913291 | TGTGGAAGCAGTAGA[C/G]AGGTGAGTAGCTAGC | 23092 |
| rs369414159 | snp | A/G | 8.91385e-05 | 0.00667542 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222479 | ACTGCTGAGCTTTAC[A/G]TGGTATCCATGACAA | 23092 |
| rs369414197 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109483 | TTTTTTTTAGACAGC[A/G]TCTTGCTCTCACCCA | 23092 |
| rs369417495 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198836 | AACTTTTAGATTCAG[A/G]GAGTACATGTACAGG | 23092 |
| rs369421042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171402 | GCCCTAGATGAGAGC[C/T]GCACTTGAGATCTTG | 23092 |
| rs369429949 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112581 | TAATCTTGTAAAACC[A/G]AAGCTCTGTATCCAT | 23092 |
| rs369445256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199909 | CCACTACTTTCTTTT[C/T]CTCTGGGAGCAGCCA | 23092 |
| rs369464916 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143134040 | AGAAGAGCAGTGACT[C/T]CAAGCCCCCGTCCTG | 23092 |
| rs369472541 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869289 | TCGGCTCACTGCAGC[C/G]TCAGCCTCCCGGGTT | 23092 |
| rs369482597 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784863 | ATCCTGTAGTCCTTA[A/G]CTAATATCTGCCATT | 23092 |
| rs369483216 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808539 | GGTAACACGGAGTCA[C/T]CAAGGTACAGAATAA | 23092 |
| rs369484911 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807752 | GCTCATGGGTATCAG[C/T]GGGACAGAGATTTGT | 23092 |
| rs369498997 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991292 | ATCTCCTGGTGTGCC[A/G]TTTGCTAAGACCTTT | 23092 |
| rs369508665 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788674 | TATTAGGTATTATAA[A/G]TAATCTTGAGATGAT | 23092 |
| rs369513011 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827414 | GCTAAAGTTTTCTTG[A/T]CTTGGCACAGAAAGC | 23092 |
| rs369527516 | in-del | -/TGT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168298 | GAAGCCTAGTAATGT[-/TGT]CTTCCCATTCCAGAA | 23092 |
| rs369530726 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908169 | GGAGAGCTGCCAGTG[A/G]CAACATAGATGTCCT | 23092 |
| rs369545351 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800946 | AAACCTCCACATTGT[A/G]TGACTCCTGTTCCTC | 23092 |
| rs369552507 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879863 | TTACAAATTTGTGCC[C/T]TGTGGGTACAGGGAC | 23092 |
| rs369559756 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012179 | TGTTCTCTTTATACT[C/T]ATCTTTCTGACCTTT | 23092 |
| rs369570310 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077435 | GAAAACCCCAGCACC[A/G]GTTCTTCTCATTGTC | 23092 |
| rs369571606 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212682 | GCCCAGCAATAAATT[C/T]GAGATAACCATTTAC | 23092 |
| rs369584797 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205351 | TTAAAGAGTCATACT[C/T]TTTACATTTTATTTC | 23092 |
| rs369611049 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128648 | CTCTGAGAGCACCAC[A/G]CAGTCCTCGGTCCCA | 23092 |
| rs369614922 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226430 | AGATTGCAGTGAGCC[A/G]AGATCACGCCCCTGC | 23092 |
| rs369619982 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132326 | GCACACAGAAAAGGA[A/G]AGAGGACCATGAGAA | 23092 |
| rs369629951 | snp | G/T | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769129 | CTATCACAAGGCATG[G/T]TTATCGCTTGTTTGC | 23092 |
| rs369633226 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831858 | CTTTTTCCTTTCTCT[C/G]TCTGCTCCTTGCAAC | 23092 |
| rs369636521 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908247 | TAAAACAACAGCAAT[A/C]ATTTTAGTATTTCTC | 23092 |
| rs369649152 | in-del | -/GAG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207032 | GTTTACTTGGACGTG[-/GAG]ATTTGGTCTGGAGGA | 23092 |
| rs369657934 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874129 | GGTCCCCGCCACTCC[A/T]GTTTCCTTAAAAAGA | 23092 |
| rs369661332 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175680 | TGTGGGAATTATTGT[C/T]TGTTTAGTATTTTTG | 23092 |
| rs369669410 | snp | G/T | 0.000153988 | 0.00877328 | stop-gained, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142894277 | CGGCAGCATTTCTAT[G/T]AAGTATCCCTGGAAT | 23092 |
| rs369671615 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense, synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207472 | GTACATGAAGACTCC[A/G]GGTAAAATCTCGGAT | 23092 |
| rs369673404 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839378 | AAGGTTTTTTTTTTT[A/T]TTTCTTTTACAGATA | 23092 |
| rs369673823 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796588 | TAAAACAGTTCTCAA[A/G]TATTACAGTGTAGTT | 23092 |
| rs369690204 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041721 | GGAGGACTGAGAAAA[A/T]GAAAAAAAAAAAAAA | 23092 |
| rs369696381 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927059 | ACAGAATAGTTCAGT[C/T]GCTAGTCTGCCGTGG | 23092 |
| rs369716957 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902097 | AAAACAAAATATGGG[A/C]CTGATTGCCCTAGAA | 23092 |
| rs369725108 | snp | A/G | 3.47548e-05 | 0.00416848 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772855 | ATCTGAGGAGGGTGC[A/G]TTTGGGTGACTGGCA | 23092 |
| rs369730310 | snp | A/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864205 | TTCAGGCCTGTGAAC[A/G]CTGTCAGTCTCTTGT | 23092 |
| rs369745291 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867488 | TGGAAATGCCTCTCT[A/C/T]CAAGCACAGTTTCTG | 23092 |
| rs369746101 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943698 | TTATTCTAACTTCTT[G/T]ATTAATTTATCAGTT | 23092 |
| rs369767924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091163 | CACGACTCTGGAGGG[A/G]GCGGCGCTTTCTTGA | 23092 |
| rs369781252 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104984 | GTTATTCCACAGTAA[A/G]TACTTTCATTTATCA | 23092 |
| rs369814766 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810985 | ATGAATAAATCTACC[C/T]GCTTCCAGTCCTTTC | 23092 |
| rs369821964 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128113 | TTCTGCCACAGGGCT[A/G]TTTTCTTTTTTTAGT | 23092 |
| rs369839852 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225469 | GCTGGGATTCCAGGT[A/G]TGAGCCGCTGCGGCC | 23092 |
| rs369856262 | snp | A/T | 0.00201491 | 0.0316764 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992440 | TTTATTTTATTTTTT[A/T]TTTTTTTTTTTGAGA | 23092 |
| rs369873309 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096051 | AATTATTACAATGTG[A/G]AAAAATAAAATCATG | 23092 |
| rs369892122 | in-del | -/AG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111974 | GACACACTTAGAAGA[-/AG]GTGGCCTCCCACAGC | 23092 |
| rs369900384 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132506 | ATATAGTGGGGGTGT[C/T]ATGCAGCCATTAAGA | 23092 |
| rs369908305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041574 | AAAGCTTCTTTCGCC[A/G]CTGATGACTGAACTA | 23092 |
| rs369917618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212928 | AGGCAGGCGGATCAC[A/G]AGGTCAGGAGATTGA | 23092 |
| rs369922660 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851492 | TGAGATTGTAATTTT[A/G]GTAGTTCAGTTCAGT | 23092 |
| rs369924652 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849922 | ACCCAGTTAGTCCCC[A/C]AACCCCACGGGTGTT | 23092 |
| rs369929953 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850606 | AGCCTCAGTCTCTCC[A/G]TAAAATAGGTATAAT | 23092 |
| rs369937156 | snp | A/G | | | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867899 | TGAGTTGGGAGGTTC[A/G]CCTCTGATGAAGGCT | 23092 |
| rs369951723 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781168 | GGCCTGTGGGAAAGG[C/G]AACTGAAGGCTTATC | 23092 |
| rs369954553 | snp | A/G/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042826 | CTCTTTTTGAGAGAG[A/G/T]CATTCACTTCTTGTA | 23092 |
| rs369959290 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093954 | GTTCAACGCACCCCA[C/T]GGGGATTTCTCACCT | 23092 |
| rs369961153 | snp | A/G | 6.69322e-05 | 0.0057846 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907672 | CATACAGTGGAATGT[A/G]TAGATATTTTATGGG | 23092 |
| rs369964746 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800370 | GTCTTTTTCTTTGTC[C/T]TTTTTTTTTTTTTTC | 23092 |
| rs369968718 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012854 | AGAGACGGAGTTTCA[C/T]CATGTTAGCCAGGAT | 23092 |
| rs370003394 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084771 | ACTTTCTCCGCTGGG[C/T]GCGGTGGCTCATGCC | 23092 |
| rs370012858 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166864 | TTGGCTCCTTGGCTT[C/T]CTGCCATCCAGTATT | 23092 |
| rs370022112 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097626 | GAGATTGAGACCACC[C/G]TGGCTAACACGGTGA | 23092 |
| rs370028266 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995906 | TCTCAGCAAAGTAAC[-/A]CAGGAACAGAAAACC | 23092 |
| rs370075018 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147483 | GGACCATTATCCCCT[G/T]AACATTATTTAAACC | 23092 |
| rs370113595 | snp | A/C/T | 1.6483e-05 | 0.00287076 | missense, synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143057679 | GGTCTCTGAAATCCA[A/C/T]AGCCTTGTTCATCGG | 23092 |
| rs370153761 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902348 | CGGTGGAAATCCCAG[C/T]CCAACCCAGCCTCCA | 23092 |
| rs370159043 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944172 | TGTGATTCCCTCCAG[A/G]GCTTCTCCTGTGTGT | 23092 |
| rs370165201 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009391 | GCTCTGGAGACAGAC[C/G]GTGGGAGTTCCTGTC | 23092 |
| rs370179340 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073891 | TCGAAGACATCTATG[A/G]TTTTATACAGCAGGA | 23092 |
| rs370190985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088203 | TCTTCACAATTGCAT[A/G]TTTCCTTTTACTTGT | 23092 |
| rs370198200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056152 | TTCAAAGAAGAGTCA[A/G]TATCCCAAAATAAAT | 23092 |
| rs370203011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207086 | ACATCCCTGGGTTTC[A/G]GTGCTCCTCTGCTCT | 23092 |
| rs370214855 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072041 | CTACTTATCTGATCT[A/G]TTATATACAAGGAAC | 23092 |
| rs370246251 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823575 | TGGTGTTATGGCAAA[C/T]TAATCTCAAAGCACT | 23092 |
| rs370251371 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806259 | CACCAGGCCCATGTA[C/T]TTTTTTATTTTTATT | 23092 |
| rs370256909 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084031 | CTGCAGGCTCTCGCC[A/G/T]TCCACGTCATTGACT | 23092 |
| rs370258709 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884509 | AGGTATTTGCCTATA[A/G]GTAAATTCCCACCTC | 23092 |
| rs370266537 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945716 | GTTACAAAAATATTA[C/G]AAAGAATTCCAGAAT | 23092 |
| rs370267487 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109698 | GCCCACCTGAGCCTC[C/G]CAAAATGCTGGGATT | 23092 |
| rs370271395 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132596 | ATATGATACAAACAG[A/C]ATAAAGAATATAATT | 23092 |
| rs370275724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924210 | ACCCTTGCTTCCTCC[C/T]TCCCTCCTCTTTCCA | 23092 |
| rs370277263 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870827 | GGGATTGGGGTGGGG[A/G]CAAGGGGTTGGGGTT | 23092 |
| rs370284748 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195801 | GTTGTAGTTTGGGTG[G/T]CTGGGGAGACTTTTT | 23092 |
| rs370324068 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909337 | CTCTCTGCAGTACAT[C/T]TTTATGCAACATGTT | 23092 |
| rs370332762 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836592 | GACATCTCGAGGCCT[G/T]TGTTTTCACAGAAGT | 23092 |
| rs370338871 | snp | C/G | 3.29603e-05 | 0.00405944 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875093 | CTTCCACCTCATGGC[C/G]CCTTTCTGTTTTCCA | 23092 |
| rs370375344 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868812 | AACCTGAAGTCTCTC[C/T]GGGGCTCGTGTCCAT | 23092 |
| rs370385302 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951048 | TTCCCTTTCCCTTCC[C/G]CTTCCCCTTCCCCCT | 23092 |
| rs370386726 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141245 | AAAAAGTTCCAGCTA[C/G]ACCCATTAAATGAAA | 23092 |
| rs370387981 | in-del | -/GGT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004067 | GGAAATCAGAAGTAA[-/GGT]GGTACAAAAACAACT | 23092 |
| rs370393590 | in-del | -/C/G | 0.0579971 | 0.161298 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099311 | CTGCCCTGGGCAGGT[-/C/G]GGGGGGCACAGGTAG | 23092 |
| rs370398600 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934959 | CTTTTTTAATACACA[G/T]TCATATCCTAGTCTA | 23092 |
| rs370400503 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039540 | TTAATTTTTTTTTTT[A/T]AATTTAAAAGAAAAG | 23092 |
| rs370404067 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898417 | CCCCAGAGAACTCAT[C/T]CTCCATGTTCATTAG | 23092 |
| rs370406707 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993295 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 23092 |
| rs370411413 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102727 | AATAACGTTCTCTGC[A/G]TATACTCCAATCCTG | 23092 |
| rs370415054 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133164 | GTTGTCATGATTTCT[A/G]TCATTTTCTTCTCAT | 23092 |
| rs370415915 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868819 | AGTCTCTCTGGGGCT[C/T]GTGTCCATCCATGTC | 23092 |
| rs370415933 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028145 | CCTGACTGAGCGTAG[A/G]TTTCCTATCTACAAA | 23092 |
| rs370417168 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935071 | ATGGATTTTATCTAC[A/G]TAGTAAATTTGAATT | 23092 |
| rs370418374 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844110 | GGCTAGAGTGTAGTG[-/TG]GCACGATCTCGGCTC | 23092 |
| rs370431493 | snp | C/T | 0.000115924 | 0.00761239 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037181 | AACTTGACTGTCCTT[C/T]TCTTGCTCTTTCAGC | 23092 |
| rs370435398 | snp | C/T | 1.65012e-05 | 0.00287234 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875061 | GCTGGAAAGGCTCCC[C/T]AAGGCCCATGACACT | 23092 |
| rs370451338 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877045 | GTTAGTATTTGGGGG[-/G]TGGGGGTGTGGCAAG | 23092 |
| rs370454321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016657 | GCAGTGAGCCAAGAT[C/T]GTGCTATTGCACTCC | 23092 |
| rs370454975 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125154 | GTTTCTTTAACCTGG[G/T]AAAACACCTCTTTTT | 23092 |
| rs370459277 | in-del | -/A | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966568 | TTGTTAAAACCCTTC[-/A]AGAACAGCCATATAG | 23092 |
| rs370461063 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062975 | TTGTGATGATGGCTT[A/G]GATGGAAAGCTCCTG | 23092 |
| rs370472021 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142771172 | GGGTGGTGCTCTGGG[A/G]CAGCGCGGGTGGGCG | 23092 |
| rs370479442 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802978 | AAGTGTTTTGGGGCC[A/T]TGCAGGGCCAACTGA | 23092 |
| rs370482904 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154061 | TTTACTAATCTTCCA[-/G]CTTTAGTTGGTCAAC | 23092 |
| rs370497709 | snp | G/T | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965243 | GCATCACAGGGAGAC[G/T]GTTAGGCCTCCGGAT | 23092 |
| rs370517787 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937800 | GTCTCAAAAAAAAAT[A/T]TACTTTAATTTTGTA | 23092 |
| rs370522871 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010599 | TTCTCTTTGGCTCAT[C/T]AACCCAAACCAGACA | 23092 |
| rs370529581 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958459 | ATTGCTTGAGTCTTG[A/G]AGTTTGAGACCAGCC | 23092 |
| rs370535904 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962965 | TCCCACCCTCCACTC[C/T]CAAGTAGGCTCCAGT | 23092 |
| rs370551709 | snp | A/G | | | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216242 | ACCGAAGCTCCGGGC[A/G]CCTCCACCTCTCACC | 23092 |
| rs370558606 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024809 | CCTGCAGCTCACAAT[A/C]GGCATGTAAGATTGA | 23092 |
| rs370574749 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889440 | CAACAAGGCGAAACC[C/T]TGTCTCTAGTGAAAA | 23092 |
| rs370583717 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105201 | ACCAACATGGAGAAA[C/G]CCTGTCTCTACTAAA | 23092 |
| rs370585435 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833179 | CTGCCTCAGCCTCCC[A/G/T]AGTAGCTGGGACTAC | 23092 |
| rs370586594 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093683 | TCTTTCCCCCTTTCT[C/T]CTCTCTGCTAGTCTT | 23092 |
| rs370592703 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068301 | ACCTGGCATCCTACT[A/G]CATTTCTCTAGGCCA | 23092 |
| rs370609912 | snp | A/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866163 | ATTTTGTAGTTTTGC[A/G]CACACAGATTAGGCC | 23092 |
| rs370614134 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929374 | TGTTATTGTATAGGA[A/G]CTGACATGGAAAGTG | 23092 |
| rs370650319 | in-del | -/AG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782667 | TGGCCAGTTTAGGTG[-/AG]GACTGTTTGGAGGCC | 23092 |
| rs370704990 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899691 | TTCCCACTTTGTAAT[A/G]CTTCAAAGGTTCATA | 23092 |
| rs370724941 | in-del | -/GGG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856220 | CTGTGGGCACACAGT[-/GGG]GGGGGCCAGCCTGGG | 23092 |
| rs370726990 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871147 | TCCTTCAGCTTCATG[G/T]GGTCCTCACTGCTTC | 23092 |
| rs370755833 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810312 | AGCTAAGCTACCATG[C/T]ATACAATAATAGTCG | 23092 |
| rs370771648 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024401 | CCTTTCCCTCAGTGA[C/T]GTGGGCTCTGTACTG | 23092 |
| rs370785943 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129291 | TTCCCTTCTTGTGTG[A/T]CTCCTTTTTTATTGA | 23092 |
| rs370808874 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048933 | AGAAAAAAAAAAAAA[A/C]AAACCTTACCCAATC | 23092 |
| rs370835842 | snp | A/G | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970922 | AAGACTAAAATAGCC[A/G]TCTTTCAGGACATAG | 23092 |
| rs370842399 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196824 | AGCTGGGAATGTGCC[A/G]TTGGGCGACTCAAGG | 23092 |
| rs370849848 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156951 | GTGCATCAATTAATC[A/G]AGCCAGTAGATGTTT | 23092 |
| rs370852632 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105576 | TAAGGGGTATGCATC[C/T]GGGTAGACGTTTGTG | 23092 |
| rs370870939 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136733 | GTCACTGTCGGGTGA[A/G]CAGATGATAATGCAC | 23092 |
| rs370877582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797895 | GAGGTGGGGCTTGAC[A/T]TTCTGCATTTCTTAC | 23092 |
| rs370888490 | snp | A/C/G | 0.000150541 | 0.00867479 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037305 | CTCATAGAAGGTCAC[A/C/G]CATCTGGTGAGGAGT | 23092 |
| rs370894781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777913 | ATGGAAGGCTGTGCC[A/G]TGATCGTACTCATAC | 23092 |
| rs370918266 | in-del | -/AC/ATAAGA | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163133 | AGAAAAAGAAAAAGA[-/AC/ATAAGA]CACTATTCGAGGCAC | 23092 |
| rs370920564 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832804 | GAGTTGAATCTGCTC[A/C]GATGCTTAAGACACG | 23092 |
| rs370930570 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228904 | TTTCTGTTCAGAGGC[C/T]TCTGAAACTTGGCTT | 23092 |
| rs370934121 | snp | C/G | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969365 | ATAGTTTGGCAGGCT[C/G]TTGGCAGGATGAAGA | 23092 |
| rs370945106 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805293 | TTTTGGTAGATGTGC[A/G]GTTTTGCCATGTTGG | 23092 |
| rs370946007 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016853 | AGTTTGGACCCTTTC[C/T]CACATGGTACAGGTT | 23092 |
| rs370952380 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014608 | GGAAAGAATGGAGAT[G/T]AATTCTATGGTAATA | 23092 |
| rs370957548 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953914 | TCGTCCATTTGGGGT[-/G]GGGGTGCTAGAACCA | 23092 |
| rs370961078 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163220 | TCTACGTATGTGGGG[A/G]AGCATTGCTGCCAAT | 23092 |
| rs370969753 | snp | G/T | 0.000215684 | 0.0103824 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879450 | GGGCTGCCAAGGTGA[G/T]AATTTTGCAAGCTTT | 23092 |
| rs370969889 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097109 | TTTGGGAGACCAATG[C/T]GGGAGGATCTTTTAA | 23092 |
| rs370971535 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217222 | AAAGTCTGTTGTTTC[G/T]TAATGATTAATCTTG | 23092 |
| rs370972211 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975934 | ACCAGTAACTGCTTT[G/T]TCTGGTGCTCAGCTG | 23092 |
| rs370975603 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899131 | TTTCACCTTTCTAAG[A/G]ACACCAGCTATGGCA | 23092 |
| rs370980892 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214852 | GAACTGCATGTGGGC[A/G]TCTGAGTCTGCATTC | 23092 |
| rs370992103 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041300 | TCTTTTTTGATAAAG[A/G]ATATTTGTATTATAA | 23092 |
| rs371005641 | snp | C/T | 0.000112714 | 0.00750629 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041909 | AGTGCCGCAGTGGCT[C/T]TGCTAGGCAGGTCCC | 23092 |
| rs371020438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165418 | CATAATGTGAATCCT[C/T]GTCCATGTCACCTCA | 23092 |
| rs371031170 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122049 | CCTCTTGTCTGACTT[C/T]TTACAAGAGCCTCCT | 23092 |
| rs371053682 | snp | A/G | 3.30426e-05 | 0.0040645 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014159 | ACAGCCAGGGTTGGG[A/G]GTAGGCTTTGAGAAG | 23092 |
| rs371059300 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029496 | TGTAACCTCAACCTC[A/G]TGGGCTCAAGCCATC | 23092 |
| rs371065715 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206349 | GCTTGTGTCATTTGT[A/G]GAAATAAGTCAAAGG | 23092 |
| rs371066409 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868959 | TGTCCAGCCCTGTCC[A/G]AGGCACTCTTTGTGC | 23092 |
| rs371076377 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084916 | TGGGCGTGGTGGCGC[A/G]TGCCTGTAATCCCAG | 23092 |
| rs371077898 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934138 | GAGTTCTAAAACTGC[C/G]TCACCAATTAATTCC | 23092 |
| rs371084070 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169733 | GGCACACGGACTCTG[C/T]GGATGGAGAAGGGGT | 23092 |
| rs371085097 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067027 | ACCTCCCCCTCCCCC[C/T]CCTCTGCCCCTCCCC | 23092 |
| rs371085770 | in-del | -/CA | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964571 | ACACACACACACACA[-/CA]AAACAACAACAGCAG | 23092 |
| rs371086193 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066983 | TGTTTGAAGGAACAA[A/G]CCACGTAGGGCTGAT | 23092 |
| rs371094974 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989386 | GAGCCTATGTGATGG[A/G]TCTCCTGAATACAGC | 23092 |
| rs371097515 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186458 | AGTGTGGACTGGGAG[A/G]TACTGATTCTTCCCC | 23092 |
| rs371104159 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223530 | CCATGTCCTCCCATT[C/T]ACCCATCTCTGCTCC | 23092 |
| rs371116652 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063832 | TCTTGCTTTCCTGAG[-/C]TCCCACAGCCTTTGC | 23092 |
| rs371120016 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036057 | GTTTACCCATATACG[C/T]TAAGAATTAAAGAAA | 23092 |
| rs371128069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144317 | TGCCTGTTCTTGTGC[A/G]CTTCTGTCAGGAGCA | 23092 |
| rs371132639 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880205 | AAGGTGGATTCTCCA[C/G]GGCTCCTTTGCCCTG | 23092 |
| rs371190222 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968036 | CATAGGTAACAGATC[C/T]GGAGCAGCTTTACTT | 23092 |
| rs371199365 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031689 | AGTGGCAGTTATGCT[A/G]AAATCCATGTCTGTC | 23092 |
| rs371206707 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965487 | TCTGGTGGCCCTGTC[C/T]GGGCATAACAGAAGG | 23092 |
| rs371207175 | in-del | AT/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879522 | TTTCTTTAAAACAAA[AT/G]TCTTCAGAAATGTCT | 23092 |
| rs371209163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025515 | TCAGTGCAAAACCAC[C/T]GGGCCTTAAGGCAGA | 23092 |
| rs371217647 | snp | A/G | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142770296 | GCCGGGCGTCCTCGG[A/G]CGGCCTGAGGGTCGG | 23092 |
| rs371234294 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123575 | CCACAATGTTGGCCA[A/G]GCACAGTGGTTCACA | 23092 |
| rs371236666 | snp | A/G | 0.000171506 | 0.0092587 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120948 | TATCTCTGTGTACAC[A/G]ATTTGTCTCATTGGT | 23092 |
| rs371239562 | in-del | -/AGTAGGT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110488 | TGTTAGCTTAAAGGT[-/AGTAGGT]TGTGTGGTTGAAGGA | 23092 |
| rs371261792 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059735 | TAGCATTTCTTGATC[A/G]TTGTCTTATCTGTGA | 23092 |
| rs371284924 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863356 | TCGTGATCCGCCCAC[C/T]TCGGCCTCCCAGAGT | 23092 |
| rs371285979 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124110 | TGAAACAAGTTTGCT[A/T]GAAACAAGCCCTACT | 23092 |
| rs371293475 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878223 | CTGGAATAATTAGTT[A/G]AGCGAAGAGTGATAA | 23092 |
| rs371303594 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946913 | TTTTAAAAGTCTTCC[C/G]TTTTGGTTATTTGGA | 23092 |
| rs371319511 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160060 | TGAGAAAAGATTTTT[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs371320071 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846039 | GTTTATTTTGTGCAC[C/T]GCAGTGAAACTGGCT | 23092 |
| rs371331671 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028513 | TATTTCATCAACTGG[A/G]AGATTTCATTCAAAT | 23092 |
| rs371355989 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011470 | GCACCTGGAACGTTG[C/T]CTGACCATTATAAGC | 23092 |
| rs371389553 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960463 | TAGCATGATGAAATC[A/G]CCCAGAGCGTGAATC | 23092 |
| rs371399226 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934141 | TTCTAAAACTGCCTC[A/G]CCAATTAATTCCATT | 23092 |
| rs371412446 | in-del | -/AGA | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004880 | CTGACCTTGGGCAAT[-/AGA]AGAAGAAGTGGGGAT | 23092 |
| rs371418337 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918266 | ATTCTCCTACCTCAT[C/T]CTCCTGAGTAGCTGG | 23092 |
| rs371429264 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990953 | CATTCTCAGATCTCA[A/G]ACTCCGTGTTGGGAG | 23092 |
| rs371430141 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009311 | TCAGCATCATCATCG[C/T]CGTCATTGTCATCAT | 23092 |
| rs371432545 | snp | A/T | 0.000307953 | 0.0124049 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885445 | GTGTTCAATTTGTAC[A/T]TGATGCTGTGGATAT | 23092 |
| rs371434818 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094706 | TGCTGCTATGTCATT[A/C]CCCTATTGGCTAGGG | 23092 |
| rs371437936 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783951 | CAGCCACACCACCCC[A/T]GCTGTGGACAATATG | 23092 |
| rs371438690 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158146 | TACCAATGAACAAAC[C/T]CCTAGTGTTGATTTC | 23092 |
| rs371439319 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859561 | AATTTTCAATAAGAT[-/C]ATCTGACTTATATGC | 23092 |
| rs371441600 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083780 | CTGGGATTATAGGCA[G/T]GAGCCACTGCACCCA | 23092 |
| rs371442249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085144 | GTCCCGGCCCCGGAA[A/G]CTCTTGATTCGCTTG | 23092 |
| rs371444646 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780915 | CTGGCAGCTTCTCCT[A/G]CAGAGCTTAGCACTT | 23092 |
| rs371446782 | snp | A/G | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968022 | TGAGTTTCCTTGCTC[A/G]TAGGTAACAGATCCG | 23092 |
| rs371457271 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094358 | TTCTTTTTTCCCTCG[C/T]GTTGCTGAGAGCTCA | 23092 |
| rs371459953 | snp | A/C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089544 | CTGAGTTTTAATCAC[A/C/G]ATACAAACTCTTCCT | 23092 |
| rs371459993 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113852 | TCATTTTGGGTTGAA[C/T]TTTCTGAGGAAGAAG | 23092 |
| rs371465551 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025074 | AATGATTAAATGTTG[C/T]GCTTTATTCTTATTA | 23092 |
| rs371473185 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146868 | GAAGCCAAGGGGATC[C/T]GGGTGAATGTGAGGG | 23092 |
| rs371484547 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101507 | CTCTTTGGGGGTGAC[C/T]CCTTCTCATCAGGTG | 23092 |
| rs371493273 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116074 | ACTTTTGTTTCTGAT[A/G]TAGTGTGGGGGTGTG | 23092 |
| rs371508031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207029 | GACGTTTACTTGGAC[A/G]TGGAGATTTGGTCTG | 23092 |
| rs371511677 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135117 | GCTTCATTAGAGATA[C/T]ACACATTGAGAGAGG | 23092 |
| rs371516035 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223289 | ACTTGAAGCACAGGA[A/T]CAAGGAATTAGGGTG | 23092 |
| rs371516657 | in-del | -/GT | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864936 | CCTTCCCCTTGCCCC[-/GT]GTGTGTGTGATATTT | 23092 |
| rs371518640 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186698 | GATACCTGTGGACCT[A/G]TTTGCCACTGGTAAT | 23092 |
| rs371520014 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144003 | CATGTTTGAGGCGGG[C/T]AAGCATTCTCACTGA | 23092 |
| rs371520743 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159302 | ATGCTGGTTAGATCC[C/T]AGAGAAGAGATCAGG | 23092 |
| rs371524382 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203838 | CAGAAAACCAAACAC[C/G/T]GCATGTTCTCACTCA | 23092 |
| rs371525720 | snp | C/T | 0.000181197 | 0.00951659 | intron-variant, synonymous-codon, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207429 | CCATCCAAACCTGCA[C/T]TTGCTTTTTGACAGG | 23092 |
| rs371538136 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105364 | CTGGGCAACAAGAGC[A/G]AAGCTCCATCTCAAA | 23092 |
| rs371554584 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011673 | CCAACCCCTTTGTTT[A/G]TGCAGGTGCTGTGTG | 23092 |
| rs371563275 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039132 | GATTTTTACTGTTTC[C/T]CTTTGACTCATCTAT | 23092 |
| rs371577138 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813831 | CAACATAGGAATTTT[A/G]GGGGCCTCAATTCAG | 23092 |
| rs371579860 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946513 | GAGACTTTGTTCATT[A/T]GAAGAATGATGGAGC | 23092 |
| rs371580954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084450 | AGCGGAATGCATGGG[C/G]TGCTTATGGGAAATC | 23092 |
| rs371585449 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046058 | AGAACTGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 23092 |
| rs371612871 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984797 | GTAAACAAACCTACC[A/G]TGCTCTCAGTCATAC | 23092 |
| rs371621561 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044998 | AGATTATTATGTAAG[A/G]TGACACTAATGAAAA | 23092 |
| rs371624419 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948231 | CAGAGAAAGTCTCAG[A/G]TCAGAAGGCTTATTA | 23092 |
| rs371629364 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994631 | CTGGAAGCAGAATCC[A/G]GTTATTGTCACCTGA | 23092 |
| rs371631495 | snp | C/T | 3.30885e-05 | 0.00406733 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902051 | GAACGTGAGTGGGCA[C/T]AGGGACAGGCTTCTT | 23092 |
| rs371650718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122283 | CTTGTTTCTGCCTTG[C/G]TGTTTCTTGGACACC | 23092 |
| rs371680301 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923879 | TTTTTTTTTTTTTTT[-/T]GATACGGAGTCCTGC | 23092 |
| rs371692741 | snp | G/T | 1.67008e-05 | 0.00288965 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907677 | AGTGGAATGTATAGA[G/T]ATTTTATGGGAAATA | 23092 |
| rs371710240 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193386 | TTGAATAGCTGCGAT[C/T]ACAGGTATACAGCCA | 23092 |
| rs371721554 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212699 | AGATAACCATTTACT[C/G]TGATCACTCTGCACG | 23092 |
| rs371722826 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942685 | TAGAGACTTTTCCTA[C/T]GAAGTGCTTAACTCA | 23092 |
| rs371725210 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076505 | TGTATATATTTATAT[G/T]TGTGGGCATATTTAT | 23092 |
| rs371739101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790305 | CTGGGCCTATAGTTG[A/G]TGACCACAGTGTTGA | 23092 |
| rs371745754 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795894 | TCAAATCCCCAGGAT[A/C]CTGAAAGTATCTGCC | 23092 |
| rs371748267 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063617 | CATGAATATTTGTTG[G/T]GCAAATGCATGAAGA | 23092 |
| rs371749246 | snp | A/G | 1.72261e-05 | 0.00293475 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120942 | GGTTGGTATCTCTGT[A/G]TACACGATTTGTCTC | 23092 |
| rs371751001 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103431 | CCATCTGACCCAGCA[A/G]TCCCATTACTGGGTA | 23092 |
| rs371751156 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881385 | GGGCTTGATACCAGT[G/T]ATCTTAATGATAGGA | 23092 |
| rs371752803 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951544 | AATCTAGTCAGACTT[C/T]AGGCCAGTTAGCTAA | 23092 |
| rs371758137 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962859 | TTACCTAGGTAAACT[C/T]ATGTCATGGGAGTTT | 23092 |
| rs371768749 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217527 | AAAATTGGGTTCTAG[A/G]GATACTTTTAATAAG | 23092 |
| rs371771132 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127681 | TTGAGTTGATTTGGG[C/G]CACCAATCTGCCTTG | 23092 |
| rs371777730 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897792 | TGAAGAAATTGAAAC[A/C]AATAAGTTTCTTTAC | 23092 |
| rs371782532 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978766 | TTTTTTTTTTTTTTT[-/G]TAAAAATTGAAAATT | 23092 |
| rs371793470 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869112 | TCTTGAACTTTAGGC[A/G]GCCATGAGGCCAATC | 23092 |
| rs371802407 | snp | G/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867072 | ATTTCTAGGTGGTTA[G/T]TTGTTCCTCAGTGGG | 23092 |
| rs371806207 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111186 | TTGTTTGCTTTCAAA[C/T]TATCCTTGTAAAAAT | 23092 |
| rs371817792 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026395 | GGCTGGTGGATAGAG[G/T]ATAAGGGAGAAGGGA | 23092 |
| rs371821755 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005672 | ATAAGTTGCTTATAT[C/G]CACAAGGTACAAAGC | 23092 |
| rs371827401 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974378 | CTAAACCCTGGCAGG[A/G]TGATGCCTACAGGCT | 23092 |
| rs371840351 | in-del | -/CA | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180370 | ACCTCGTGATCTGCC[-/CA]CCTCAGCCTCCCAAA | 23092 |
| rs371857169 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947122 | AAAAAAAAAAAAAGA[A/G]AGAGAGAGAGATGGG | 23092 |
| rs371865790 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226575 | TAAAACCCTGACTTG[C/G]TCAAGACAGAAGATC | 23092 |
| rs371871993 | in-del | -/CCGTTTTATGACA | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191926 | AGAATGAGAGCTGTA[-/CCGTTTTATGACA]TCAGATAATTCTGAC | 23092 |
| rs371875040 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779781 | GTGCCAAGGAGACTG[G/T]CAAACAGATAGGACC | 23092 |
| rs371877054 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212848 | CTTGGAGAGCTTTTT[A/T]AAAATACTGATGCCT | 23092 |
| rs371879362 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218591 | GTGTACACAGGGATG[A/C/T]ATGGTGTACATGGGT | 23092 |
| rs371880079 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915517 | GCACTCGCCACCATG[C/T]CCGGCTAATTTTTTG | 23092 |
| rs371883625 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800716 | AATAGACCTGCTTAT[C/G]GTGTCAGTTCAGTAG | 23092 |
| rs371890802 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128193 | GCATTTGAACACATA[C/T]ATTCCCCCCAATAAA | 23092 |
| rs371895405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926593 | GGGAGTGGTAGGCCA[C/T]TTTGTTGCGTTACTC | 23092 |
| rs371901944 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217000 | GTGGGTGGGGTGGGG[A/G]GTCTTTTTCCTTGTT | 23092 |
| rs371918067 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004005 | GCCTCGTGGTCAGAA[A/C]AAATTTATAGACAAA | 23092 |
| rs371922101 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816473 | TGAAGCCACAATTCA[C/G]AGGAGGATAGTCACT | 23092 |
| rs371937568 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848513 | AGGTGGTTCTCCAGC[C/T]TTGGCACATCAGCTG | 23092 |
| rs371942575 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980002 | ACCAGATCAAGATGT[A/G]GAACATTTCCAGCAT | 23092 |
| rs371945780 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781859 | TGGGACTACAGGTGC[A/G]TGCCACCATGCCCGG | 23092 |
| rs371964719 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822898 | GGAGACCAGTCAGTA[A/G]ATAGTTGCTGAGTGA | 23092 |
| rs371966674 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224540 | TTTCTTCTCAGGTGT[A/G]TTTCTTGGTACCCCC | 23092 |
| rs371971390 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993700 | CTGGAGTGCCATGGC[A/C]TCATGATCACAGCAC | 23092 |
| rs371974304 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009125 | GTTCAGAGAGAATAT[A/G]AAGTGTTACTTCTAT | 23092 |
| rs371980471 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221528 | GAAGCTGGATTGATT[A/G]ATTGAGACAGGGTCT | 23092 |
| rs371982004 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085916 | AATATTTAAATAGTT[G/T]TAGCTACATTTTCCC | 23092 |
| rs371982570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820608 | CTCAAACAGCAGGGG[C/T]GTATCTGTGCAGCAG | 23092 |
| rs371988333 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923097 | TGGAKTTTTTTTTTT[-/TT]TCTTTTAATTAAATG | 23092 |
| rs371997647 | in-del | -/TTAT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837876 | GAAAAGAATAGTTAT[-/TTAT]GTACATAATTTCACA | 23092 |
| rs372003847 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049338 | ATTGTGATTATTATT[G/T]TGCTGTTTATAATGC | 23092 |
| rs372005147 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165244 | ATCAGGGCCCCTAGG[A/G]GCCCTGCACTGGTTT | 23092 |
| rs372011011 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147954 | CCCATAGTCAGGACA[A/G]TTAGTTTGGGGGCTG | 23092 |
| rs372022438 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162024 | ACGTCACAGACAAAG[A/G]TGAGTAAAGCCCACT | 23092 |
| rs372024092 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941157 | GGTCGAATGGTAGTT[C/T]TGTTTTAAGTTCTTT | 23092 |
| rs372032953 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987755 | TCTATTGAGATAATC[A/G]TGTGGTTTTTGTCTT | 23092 |
| rs372033338 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050255 | GTTAAAAATTTGTGT[A/C]CCTTTTTTGTGTGTT | 23092 |
| rs372066159 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153023 | CTGTGAGTTTGTGAC[C/T]GCGGAGTCATGGGCA | 23092 |
| rs372068665 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198342 | AGTGTTTTCTTACAA[A/G]TAAATTCACATATTG | 23092 |
| rs372070632 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772493 | ACTTTTGGTGTGATT[C/G]TGGTGTACTGGGTAC | 23092 |
| rs372082216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110208 | GTTTCATCATAGCAC[C/G]ATATATTTTCTTTGC | 23092 |
| rs372085582 | in-del | -/A/AA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030609 | TCATCACAAAAAAAA[-/A/AA]TGAGAAAGTGGAGGA | 23092 |
| rs372088600 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882584 | TAGGTTCTTGGGACG[C/G]TTACCTTCATGGCAC | 23092 |
| rs372091961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142436 | TGAGCCACTGCGCCC[A/G]GCCTACTTTTCAACT | 23092 |
| rs372094837 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193240 | TGCTTATTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs372095413 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017713 | TTTTATGCTGTGGCT[A/T]CTGATTACTGCATAA | 23092 |
| rs372103395 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812198 | GCTGTAAGGATCTTT[C/T]TAACCCAGTTCTTTA | 23092 |
| rs372104278 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168976 | TTCTCAAACTGTAAG[A/T]GAACTATGGAAACTG | 23092 |
| rs372107347 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801687 | GATGAAGAATTCCCA[C/T]CCCTCCCCCAGCCCC | 23092 |
| rs372108409 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108694 | CTCATTTAAAAAATC[C/G]CCACAAAAGGAGATA | 23092 |
| rs372110716 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849228 | TAGCTAAAGCAATTC[C/T]AGTAGGTTTTCATTG | 23092 |
| rs372114641 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776147 | TTATTGTTTTTATTA[C/T]TTGTGGAGATGGGGG | 23092 |
| rs372119249 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806856 | TTGGAACTAACCAGC[A/C]GTTGACTCATTTCAG | 23092 |
| rs372120157 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804262 | TTATATACACACACA[C/T]ATATATATTACAAAT | 23092 |
| rs372127980 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788037 | CTTACTCTATTGCCC[A/T]GGCTGGAGTACAGTG | 23092 |
| rs372130123 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820133 | AAATGGAATCCACGA[A/G]TGTGCATTTCACATG | 23092 |
| rs372150473 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809734 | GAGCCATCCACTCCT[A/T]CATTCATCTGTCCAT | 23092 |
| rs372150511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222058 | AGCTTCAGAAAATCC[A/G]TGAAACCCCTAAAAT | 23092 |
| rs372178715 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158119 | TCTTATTTGCTCTCA[G/T]ACTGCTCCCCCTACC | 23092 |
| rs372180857 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190880 | ATTGACTACTTATAC[A/G]CGCCAGAACATGGGT | 23092 |
| rs372197133 | in-del | -/TTTTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142135 | ACTCTACTTTTCACT[-/TTTTT]TTTTTTTTTTTTTTT | 23092 |
| rs372197247 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057565 | AGTGCTCATCCTTTG[A/G]TTTCCCTTAATTTTT | 23092 |
| rs372213925 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987664 | TATTATTTTGAGATA[C/T]GTCCCATCAATACCT | 23092 |
| rs372220864 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910058 | TTTTGGAACAAATCC[A/T]GACACATAATGGGTG | 23092 |
| rs372222722 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953004 | ATGAGTCACAGCACC[C/T]GGCCCCAACTGTGCT | 23092 |
| rs372238384 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178280 | GCTGAGATTACAGGC[A/G]TGAGCCACCGTGCCC | 23092 |
| rs372238650 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799402 | AATGCTTGTCAAGAC[A/G]AATGTCTTAATTTGT | 23092 |
| rs372240457 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940843 | GCACTTTGGGAAGCC[A/G]AGGTGGGCAGATAAC | 23092 |
| rs372250602 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906886 | AACAATTTTTTTTTT[-/TT]AACAATTTCTGCTGT | 23092 |
| rs372257317 | in-del | -/TA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945868 | TCTCACTAATATATA[-/TA]TATTTTTCTGGTCCA | 23092 |
| rs372273381 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100670 | CTTGGCAGTCTCCTT[A/G]GGGACTCTGCTGGCT | 23092 |
| rs372285895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815344 | CCATGCCTGGCCAGA[A/G]TTACATAATTTTTAT | 23092 |
| rs372301500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792342 | TTATTTTTTAGGCTT[A/G]CTAAGTAAAATTTAA | 23092 |
| rs372322371 | in-del | -/AGAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118960 | AAAAAAAAAAAAGAA[-/AGAA]GAAAGAAAAACAGTG | 23092 |
| rs372330481 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188740 | CTGTGACCATGAATA[A/C]CGTTGCAAGTGAATT | 23092 |
| rs372334261 | snp | C/T | 3.42132e-05 | 0.00413587 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894224 | TTTTCTCTTAAATTC[C/T]ATCTTGTTTGTAGGC | 23092 |
| rs372337876 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823327 | ATGATCAGTATATGC[A/G]GATTACAAATGTTGG | 23092 |
| rs372346627 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873021 | GAAACTGCACTGACT[A/G]TGTGGAGGGTCAGTG | 23092 |
| rs372361619 | snp | A/G | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964587 | AAAACAACAACAGCA[A/G]CAAAAAAAACCGATG | 23092 |
| rs372380456 | snp | A/G | | | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859468 | TTTTAATCTGCCCAT[A/G]TTCTTCTAAAAAGGA | 23092 |
| rs372385718 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799423 | CTTAATTTGTAATAT[A/G]GTGAGAAGTTTACCC | 23092 |
| rs372400096 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953252 | TTAATTCAGTGAATA[C/T]TTATTGGGTATAAAC | 23092 |
| rs372411567 | snp | C/T | 8.30654e-05 | 0.00644405 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903678 | GAGAAACGTGAGTGC[C/T]TTGACTAGCAACAGC | 23092 |
| rs372426067 | in-del | -/CT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093506 | TTTCTATCTCTCTCT[-/CT]TTCTTTCTCTCTTTG | 23092 |
| rs372426289 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882134 | GAGTAGCGTAGAGAG[C/T]GGGTCTACAGCTAGA | 23092 |
| rs372432887 | in-del | AT/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027542 | CTTACTGGTTTTAAA[AT/C]CAATTCATCCATTTT | 23092 |
| rs372443447 | snp | A/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970660 | GCCAGGGTGTAACAG[A/T]CAGGGGAGCCATCTG | 23092 |
| rs372455399 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171074 | GGAGCTATAATAAAG[C/G]ACAGAGAATATAAAG | 23092 |
| rs372464004 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227351 | GCAAACTTGACAATC[A/G]TCACTTACCTCGACA | 23092 |
| rs372464189 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792956 | ATAACTGATGTTCAT[C/T]GAAGGCAGAAAGGTT | 23092 |
| rs372470617 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209617 | AAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT | 23092 |
| rs372482330 | snp | A/T | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007820 | TGGCTATTTTTATGT[A/T]TGATTGCTGTTTTAA | 23092 |
| rs372485954 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024573 | AATATTTCCCCCACT[A/G]CCACCGAGTACAGGC | 23092 |
| rs372511598 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770418 | CTGTGAGAGGGCGCT[C/G]GAGGCTGCCGAGAGC | 23092 |
| rs372517249 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795667 | ATTACAATTTATCGC[A/C]TATCAAGGCCTCTTA | 23092 |
| rs372530987 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800385 | TTTTTTTTTTTTTTT[C/T]TGAGATGGAGTTTCA | 23092 |
| rs372538849 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768747 | TCTTTCTCATCTTTG[A/G]CAAGTGAAGAACAAT | 23092 |
| rs372539236 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954941 | AATAATCACTTTTGA[A/G]GAGCAAGAGGGAAAC | 23092 |
| rs372552269 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996211 | ATGAAAATAGGTTTG[G/T]GGCTGGGTGCAGTGG | 23092 |
| rs372572760 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187809 | TGGCATGTCATAAGT[A/G]CACTCTATCCATTGG | 23092 |
| rs372576803 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150318 | GTTCCTGTCTTCCCC[A/G]AGAGTTCACAGTCTA | 23092 |
| rs372593801 | snp | A/G | | | intron-variant, missense | ARHGAP26 | GRCh38.p7 | 5:143057919 | TGGAGAACAGCAGCA[A/G]ATGCCAGATGGCCTT | 23092 |
| rs372594209 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064794 | AGGAGAGAGAAAGAT[A/G]TCAGTTCAGTTTAAA | 23092 |
| rs372597429 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792850 | CTTAATAAATAGTAA[A/C]ATTAAAGTTCTTTCT | 23092 |
| rs372597647 | snp | A/G | | | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229128 | TTTTTGGTGACAACC[A/G]CCGTGCTTATTTCTG | 23092 |
| rs372609282 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108192 | ATAAAGGTGTAATCA[A/G]TTCAGATTGTTTCTA | 23092 |
| rs372610263 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783491 | ACATTTTTTTTTTCT[G/T]TAAAAACATTCAGGA | 23092 |
| rs372617963 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091164 | ACGACTCTGGAGGGG[A/G]CGGCGCTTTCTTGAC | 23092 |
| rs372631172 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130779 | GTGTCAGAGTTAAAT[A/C]AACAACAGTCACTTG | 23092 |
| rs372636345 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850605 | GAGCCTCAGTCTCTC[C/T]GTAAAATAGGTATAA | 23092 |
| rs372654288 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205514 | CTTGCAAATAGGGTA[A/G]GTATCTAAAGGAAAC | 23092 |
| rs372665753 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020882 | GCTGACCTCATGATC[C/T]GCCCATCTCGGCCTC | 23092 |
| rs372671216 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168897 | TAGCCTTCACTTACT[A/G]TGCTAAACCTGCTAA | 23092 |
| rs372674723 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084812 | ACACTTTGGTGAGGC[C/T]GAGGTGGAAAGATCA | 23092 |
| rs372687721 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112362 | AATTTTAGCTCAGAG[A/G]TGGGAGAGTACAGGG | 23092 |
| rs372692431 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992966 | GAAGAGCTTCCTGAG[A/T]CCTAAGTTCTTTATT | 23092 |
| rs372693796 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876777 | GCAAGACCCTGTGTC[-/A]AAAAAAAAAAAAAAA | 23092 |
| rs372694860 | in-del | -/AT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105542 | GTGTGTGGGAATCAT[-/AT]GTGGGTGTATATATG | 23092 |
| rs372696169 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803053 | CATGCGCAGACTGTC[A/G]TAAAGTATGGGAACC | 23092 |
| rs372703370 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935985 | TACTCAGCAGAGGAC[C/T]GGAAGTCCTAGTCAG | 23092 |
| rs372714409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909262 | CTTCAGCTTAAATAG[G/T]TTTTCATTTGTGTCT | 23092 |
| rs372716316 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950672 | GTCATAAGAAGTTCT[G/T]TGCATCTGCCCTTGT | 23092 |
| rs372717017 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024959 | AGTTTCTTTGTCTGA[A/G]GGTGGGAATAGTTTT | 23092 |
| rs372717377 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977797 | TCACGGAGGAAGTCA[A/G]TGAGTCAGAGATGCG | 23092 |
| rs372723879 | in-del | -/AC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936109 | AGAAAATCCCAAGGA[-/AC]ACACACACACACACA | 23092 |
| rs372726286 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898156 | TATATATGTGTGTAT[A/G]TATATATACACACAC | 23092 |
| rs372728163 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856856 | TGTTATCTGTGGGGA[A/G]TCCTGGAACTAGTCC | 23092 |
| rs372729843 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142894278 | GGCAGCATTTCTATG[A/T]AGTATCCCTGGAATA | 23092 |
| rs372733642 | snp | C/T | 5.00872e-05 | 0.00500411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207505 | TGACCAATCTGTTCC[C/T]GTTTATCCAAAGCTG | 23092 |
| rs372750535 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086282 | ATTACTAAAATGACA[C/G]AAACCCATTGTTGAT | 23092 |
| rs372760663 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050466 | GCTTCACCCACTTAC[C/T]GCCGATCCAGCCATG | 23092 |
| rs372767807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871509 | AGTGCAGACTTTGTG[C/T]GTTCTCATCAGGGAA | 23092 |
| rs372779492 | in-del | -/GG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838520 | CCACGCTTATTGGCT[-/GG]GTGTCACCTCAGACA | 23092 |
| rs372786115 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888225 | ATAGCTTAGTGGTAG[C/T]GAGTTAACTCCAGCA | 23092 |
| rs372817847 | snp | C/T | 5.06864e-05 | 0.00503395 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907839 | TTGATGTTTGATTTG[C/T]TTGGCTAACATATAA | 23092 |
| rs372823934 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006924 | TTACAGTAACTTCTC[A/G]GGGGTGTTATTAAAA | 23092 |
| rs372827247 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997640 | CCAGGCTGGTCTCAA[A/G]CTCCTGATCCCAAGC | 23092 |
| rs372848706 | in-del | -/AA | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890118 | TCCAGCCTGGGTAAC[-/AA]GAGCGAAACTCCGTC | 23092 |
| rs372857864 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138462 | TTTAGTGAGGAAGGA[C/G]CTAGATATCAAAGTT | 23092 |
| rs372864388 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807992 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 23092 |
| rs372882777 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066427 | ATACAGTAATAGTGC[C/T]CACCCTTTTAGAGTT | 23092 |
| rs372883132 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128704 | TGTGCTCAACTGTTG[C/T]AGGTCTACTTTCCTA | 23092 |
| rs372888032 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900923 | ATGGGATAGTCCCCA[A/G]ATACCATGGAGCTGT | 23092 |
| rs372901474 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916825 | GTGAGGCAACTGGTA[A/G]TATCAGAGCATTTCC | 23092 |
| rs372901950 | snp | C/T | | | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194487 | TTCTCTTAAGTTAAG[C/T]ATTTATGTATGAAAC | 23092 |
| rs372902655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221015 | TCTATTCTCTCCAAA[C/T]AATCTTGGAAAATTG | 23092 |
| rs372914391 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005420 | GGCTGAGTTTGGCTT[C/G]GGCCAATCATATGTG | 23092 |
| rs372928875 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990796 | ATTGCAGAACAGCAA[A/T]TGTTGCTTCCTGATC | 23092 |
| rs372937341 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804807 | TGAACAGATTTTTTT[C/T]TTTAAACTTTTTATT | 23092 |
| rs372939298 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012119 | TTAGGTATATGCATT[A/G]ATGCCTTTTCATTCA | 23092 |
| rs372944589 | snp | C/G/T | 3.311e-05 | 0.00406867 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054537 | CTAAGGTAGGGACTT[C/G/T]CCATTTGCAAGGCAG | 23092 |
| rs372950836 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893391 | GTTTTTCTGTGCCTT[C/G]ACTTGACATAATGAC | 23092 |
| rs372967664 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019680 | CCAGTGCAAGGGAGT[A/G]AGAGAAGGGCAGGCT | 23092 |
| rs372991786 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868365 | CTTGGGAGGGACTTT[A/C/T]GTCTTCACCTCCAGA | 23092 |
| rs372993247 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994839 | CTCTCCATTTTATAG[A/G]TGGGGTAATGAGGCA | 23092 |
| rs373003372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971583 | TACTCTTTTCTGTAC[A/C]TGCTGATTTTTTTTT | 23092 |
| rs373025137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031809 | TACTGCAGTCTCTGC[C/T]TCTTGGGTTCAAGCG | 23092 |
| rs373031025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200723 | TACAAGGCCGTCAGT[A/G]ATTTTCATTATTAGA | 23092 |
| rs373040069 | in-del | -/TT/TTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011303 | ACAATAAACCCCCGC[-/TT/TTT]TTTTTTTTTTTTTTT | 23092 |
| rs373050075 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121578 | GGGATATTAAACTTT[A/C]TTCATTTGTGTTGCA | 23092 |
| rs373084284 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041722 | GAGGACTGAGAAAAT[A/G]AAAAAAAAAAAAAAA | 23092 |
| rs373089648 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870555 | ACTTCTCCGAGCTCC[A/G]AACAGTTATTCATGC | 23092 |
| rs373107339 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128700 | GAGCTGTGCTCAACT[C/G]TTGTAGGTCTACTTT | 23092 |
| rs373114557 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113698 | AAGAAACAGTGTTTA[A/G]TCCAGTATCACTCCC | 23092 |
| rs373121223 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821568 | ATTATCATTCCTGGA[C/T]CAGCACCATCAACAT | 23092 |
| rs373130463 | snp | C/T | 6.71175e-05 | 0.0057926 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143222431 | CATCCCTGAGAATTA[C/T]GTGGAGTTCCTCTAA | 23092 |
| rs373139809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912976 | CCATCATGATCCACC[C/T]GTACTAAAGATGTTT | 23092 |
| rs373144103 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101782 | AATTTCTGCTGCATG[C/T]TCTACACAAAATTTA | 23092 |
| rs373145934 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923653 | ATGCAATTTAATATG[C/T]CAAAGATGTCTTTGG | 23092 |
| rs373147161 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065424 | AATTGTGGCTGAAAC[A/G]TGGCAGCTGGCAGAC | 23092 |
| rs373179478 | snp | C/G/T | | | intron-variant, downstream-variant-500B | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142972115 | TGAACCTGCGAGGCG[C/G/T]AGGTTGCAGTGAGCC | 23092 |
| rs373193587 | snp | A/G | 1.73773e-05 | 0.0029476 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772885 | AGTTTTCCTACCACT[A/G]GTTTTTGGGGGCAAG | 23092 |
| rs373198275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158746 | GCTGGTGATGGGGCT[A/G]TTCCCTGGCTGTTGT | 23092 |
| rs373200789 | snp | C/G | 0.000362379 | 0.0134558 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932035 | ATATCCATGTCCCTC[C/G]TTTCTCTGCAGGCCA | 23092 |
| rs373231174 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115561 | CTGGGCAGGATACCA[A/G]GCGAAACTACCAACT | 23092 |
| rs373240209 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826155 | AGGAGGGGGATATGA[C/T]ATGTGATCAAATTGT | 23092 |
| rs373244589 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793306 | GAGGCTTGAGGGGTC[A/G]TAGCTTTGGTAGGAG | 23092 |
| rs373261819 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856670 | GTACAGACTTTTTTT[-/T]CTTTTTTCTACTCTC | 23092 |
| rs373265449 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140752 | TCGGTGGGGGTGGGG[G/T]TGGGGGCAGGAGTGG | 23092 |
| rs373282890 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787993 | ATGATTATTAACCAA[-/T]TTCTTTTTTTTTTTT | 23092 |
| rs373290768 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928461 | ATCTCATTTAATCCC[A/G]TGCAGGAGCTCACTA | 23092 |
| rs373301892 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999066 | GGTGAAATATTAAAA[A/C]TTATAGGGACTAAGA | 23092 |
| rs373310003 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012897 | CTGACCTCATGATCC[A/C]CCCGCCTGGGCCTCC | 23092 |
| rs373313335 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788720 | GGATGTGCTTAGGTT[A/G]TATGCAAATACTATG | 23092 |
| rs373317587 | snp | C/T | 4.94197e-05 | 0.00497066 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142875135 | GCAGGAGTTTGCCAC[C/T]GTCCTCAGGAATCTT | 23092 |
| rs373332435 | snp | C/T | 1.73933e-05 | 0.00294895 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133917 | CTTCAGGCCTGTTTT[C/T]TTCCCAGTCCACAGA | 23092 |
| rs373338867 | snp | A/C | 3.34549e-05 | 0.00408978 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057783 | TAGCCTTTTTCTTAC[A/C]CCTGAAAGTTCTTAT | 23092 |
| rs373339433 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074921 | ACAGCCTAGAGGGTA[A/G]CATGGGCCTGTCCAC | 23092 |
| rs373348897 | in-del | ACACCTAACTCA/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109161 | GGTAGCAGGTAACTC[ACACCTAACTCA/G]CACCTAGAAGCTCTT | 23092 |
| rs373351457 | in-del | -/ACCGTTTTATGAC | 0.0356815 | 0.128715 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191925 | CAGAATGAGAGCTGT[-/ACCGTTTTATGAC]ATCAGATAATTCTGA | 23092 |
| rs373387082 | snp | A/T | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961623 | ATGGGTATTACTGGC[A/T]ATGAATTTGGCAACT | 23092 |
| rs373396850 | snp | A/G | 0.00031342 | 0.0125145 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056090 | TCAAAGCAGCAAGTA[A/G]GTCTTTTTTGTCTCA | 23092 |
| rs373407600 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036368 | TTCCAGCCTTGTGTG[C/G]TTCTCTGCTGTGGAA | 23092 |
| rs373413418 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993336 | CACCGCGCCCGGCTA[A/T]TTTTTTGTATTTTTA | 23092 |
| rs373415713 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813277 | CTACCTATCCTCTCT[A/G]TGTAATTGACATAAG | 23092 |
| rs373432112 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108316 | ACCAGTAATTTTCAT[A/G]GATGTTAGAGCTCTA | 23092 |
| rs373439155 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829487 | TGTGAATAGTTGTTA[C/G]AATTCTCACCATTAA | 23092 |
| rs373451874 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870150 | ACAGCAGGGTTATAT[G/T]AGGAGGGTGCCACGA | 23092 |
| rs373459498 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953918 | TCCATTTGGGGTGGG[A/G]TGCTAGAACCACACT | 23092 |
| rs373462759 | in-del | -/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088477 | AAATTGTTAAAAAAA[-/G]AAAAGTGGTTATGTC | 23092 |
| rs373481259 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884301 | CCGTGACTTTTCACA[A/G]GTTCACCTCTTTGGG | 23092 |
| rs373488343 | snp | A/T | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769547 | TAGCACACACAGCAC[A/T]TAGTAAGTGCTCAAT | 23092 |
| rs373506061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864487 | AAGGAAATTGTAAAT[C/T]TGTAGAAGCATTAGG | 23092 |
| rs373541710 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899060 | TTTCTTGGCTTATAG[A/T]TGCCTCCCTCCAGTC | 23092 |
| rs373546598 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096356 | ACGTTTTCTTGAAAG[C/G]ATAAATTTTATCATT | 23092 |
| rs373561953 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910641 | CTATTTGGGAGGCTG[A/T]GGCAGGAGAATCGCT | 23092 |
| rs373570152 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953149 | CCCACACCAACCAGG[A/G]TTGTCCTCACTGGAT | 23092 |
| rs373583446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004647 | CCACCCTGACCTTCA[C/T]CTCTGTTCAGCACAA | 23092 |
| rs373610627 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805333 | TCTCGAAGTCCTGAC[C/T]GCAGGTGAACCACCC | 23092 |
| rs373612388 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867713 | ATGCTCCTGCTGGTG[C/G]TAGCTCTCCCTCCAG | 23092 |
| rs373623128 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063627 | TGTTGGGCAAATGCA[A/T]GAAGAGTCTCTTGAC | 23092 |
| rs373626210 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053918 | TGCTTTACAGTCATC[A/G]TTGTCATATAAATCG | 23092 |
| rs373633242 | multinucleotide-polymorphism | AG/CA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154060 | ATTTTACTAATCTTC[AG/CA]CTTTAGTTGGTCAAC | 23092 |
| rs373635139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127013 | ATATTGAATGCTGTC[A/G]TGGTCCAAGATCTCA | 23092 |
| rs373636480 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823532 | CTCTTTTTGTTTTTG[-/G]AACAAACTCTGTTAC | 23092 |
| rs373639978 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011517 | TTAAATACATGGATA[A/T]GTAAACGAATTGCAA | 23092 |
| rs373669668 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210729 | AGTGCCATATGATGG[C/T]GAATGGGTCATCATT | 23092 |
| rs373669932 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151183 | ATGATTCACGTCTTA[C/T]GTCTTCAGGGAAATA | 23092 |
| rs373692311 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031499 | TTGGTGATAATTTGG[A/G]ATGGGAGGTAAGAAG | 23092 |
| rs373693201 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145677 | GTTTCTGTTCAAAAA[C/T]GAAGCTCTTAAAATA | 23092 |
| rs373695559 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003701 | AAATATTTGTGGAGT[A/G]AGGAAAAGGGAAATA | 23092 |
| rs373719970 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226507 | AAAAAAAAAAAAAAA[-/G]AATGCCATGCCAGGA | 23092 |
| rs373729374 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024011 | GTGCTGACTTTCTAC[A/G]CCTCACTTTTCATTA | 23092 |
| rs373740575 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038546 | ATAAGGATGTTTACA[C/T]CGTGGTGATGTTAAG | 23092 |
| rs373744546 | snp | A/G | 1.66305e-05 | 0.00288357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207496 | CTCGGATGATGACCA[A/G]TCTGTTCCCGTTTAT | 23092 |
| rs373747718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923658 | ATTTAATATGCCAAA[A/G]ATGTCTTTGGGCTTC | 23092 |
| rs373759255 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993255 | GCTCACTGCAAGCTC[C/T]GCTTCCCGGGTTCAC | 23092 |
| rs373766486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085001 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 23092 |
| rs373767920 | in-del | -/GAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007194 | CAAGACTCTGTCTCC[-/GAAA]AAAAAAAAAAAAAAA | 23092 |
| rs373772532 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055666 | AAGCCGCTGGGAAGA[A/T]CAAGACTTGCAAATA | 23092 |
| rs373794316 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122135 | TGAGATTTTTTTTAA[C/T]GTTAAGCCAGATGGT | 23092 |
| rs373802301 | in-del | -/GCGC | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963220 | TGTGTGTGTGTGTGT[-/GCGC]GTGTGTGTGTGTACC | 23092 |
| rs373803292 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000704 | ATGCAGCCATAAAAA[-/A]GAATGAGGTCATGTC | 23092 |
| rs373805164 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014615 | ATGGAGATGAATTCT[A/G]TGGTAATATTCCTCT | 23092 |
| rs373806078 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059403 | AGCCAGTGTTGCGTT[C/T]TTCCTACTTTTAAAT | 23092 |
| rs373820406 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832056 | GAAGACATACCAAAA[C/G]TGTACACATGTCCTT | 23092 |
| rs373822691 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877038 | TTGGCTGAGTTAGTA[C/T]TTGGGGGTGGGGGTG | 23092 |
| rs373829603 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143207284 | TGCCCACCTCATCCA[C/T]GTCCAGCGACTCATC | 23092 |
| rs373853598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173255 | ATATGGAGTGCCCTC[A/G]AACTCTTTGGCCTCA | 23092 |
| rs373854678 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222671 | CAATCAGCAGAGGAG[A/T]GCATTTGATAACTAA | 23092 |
| rs373863632 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211338 | TTATTCTGCCATCCA[A/G]ATCTAACTAGGTGTC | 23092 |
| rs373871825 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979723 | AAAGAGAGTATTTGT[A/G]TGAGAATTAAGGGAA | 23092 |
| rs373873482 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994278 | TCCTTGGCAAGAAAT[A/G]TGGCAACACAGATTC | 23092 |
| rs373877914 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142771295 | CAGCTCCCTTAGGGG[C/T]AGAGTTGCTCAGCCT | 23092 |
| rs373890229 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201321 | CTCTGAGGGTTGTAG[C/G]AATGCCTTTAGCAGT | 23092 |
| rs373912218 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819495 | CATGTGCAGACTGAG[C/G]CTGTTAGGTCTTCTG | 23092 |
| rs373912684 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878974 | TTTCTTTGTTTATTT[A/G/T]TTTTTAACCTAGACT | 23092 |
| rs373913686 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910187 | CCCTGTTTGATCCAG[C/T]TTTCCTCCTTTTACA | 23092 |
| rs373917198 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788658 | CAGAGCTATTACCTT[G/T]TATTAGGTATTATAA | 23092 |
| rs373945318 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150627 | GGAATTCCTCTGGTA[C/G]CACTACCACCAAAAA | 23092 |
| rs373948429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912640 | GGCCCAGGAGACAAA[A/C]GTAAGCAAAATTTGA | 23092 |
| rs373960343 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179733 | TGGAGTTATTTCCAA[C/T]GTTTGGTAATTCCAC | 23092 |
| rs373962462 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784990 | GGAGTGCAGTGGCGC[C/G]ATCTCGGCTCACTGC | 23092 |
| rs373971652 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945736 | AATTCCAGAATACTT[C/T]CCACCCAGATAACCT | 23092 |
| rs373974950 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903177 | AGCTGGAGAAATGAA[C/T]GCCTAGGTCCTTAAG | 23092 |
| rs373978367 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033496 | ACAAAAAAAGGTTCA[A/G]TGACTGATTTGCCTC | 23092 |
| rs373983546 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040793 | CATGAGCTTGGCATG[C/T]TGAGGTGACAGGAAG | 23092 |
| rs373994497 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053779 | TCCACCACTTTAACC[-/C]AACCACTAATTTAGA | 23092 |
| rs374024564 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785332 | TCCTCAGAATGCTGC[A/G]GTTCCAACACCAGGA | 23092 |
| rs374026785 | snp | C/T | | | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143068733 | ACTATCCCATTTTTC[C/T]GTGCTTTTCCCAGAA | 23092 |
| rs374028609 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050117 | ATGTTGTTGGTGGGC[A/G]GAGGGCCACCACCTA | 23092 |
| rs374037434 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903111 | GAGTGAAGGAACTCC[A/C]CTTTTAAGGAGGGAC | 23092 |
| rs374038291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161679 | CCTGCCTGTAGGACA[A/G]TAAGATCACCTGCTT | 23092 |
| rs374042008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856146 | GACTGACCTGGTCCC[C/T]GTCTTCTTGGAGCTG | 23092 |
| rs374045707 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875545 | TTATTGAACCTGATC[A/C]AGAGCTCTTTGAGGG | 23092 |
| rs374053167 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918801 | TCAAAAAGCTAAAGT[C/T]AGTAGAAATTCTTTG | 23092 |
| rs374058728 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832036 | GGCTCCCTGTTGTCT[A/G]TTATGAAGACATACC | 23092 |
| rs374082433 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159989 | TCAGAAATACATTTG[C/T]TTGGTTTTGAAATGA | 23092 |
| rs374087726 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205729 | CCTTAGAGAAGCCTC[A/G]GCTTAGCCCAGGTTT | 23092 |
| rs374091867 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176022 | AGGAGGCCGAGGCAT[A/G]GGAATCACTTGAACC | 23092 |
| rs374093309 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220732 | GTGATCTGAAATTGG[C/T]CAACTTTGGAGGCCA | 23092 |
| rs374094900 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797542 | TGATTTTTTGTATCA[C/T]AGCTGTCTGTGCTCA | 23092 |
| rs374106373 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895697 | TTCATCAAGACTCCA[A/G]TTGGTGGCCAGGCAC | 23092 |
| rs374109096 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213598 | AGCTTTCAACAGGTT[A/C]TGTTGGGAGTGTGTT | 23092 |
| rs374116298 | in-del | -/AG | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768905 | TTGTAGAGATGGGGG[-/AG]GGGTCTCGCTGTGTT | 23092 |
| rs374118455 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786261 | GCTGGGATTACAGGT[-/TT]GTAAGCCATGGTGTT | 23092 |
| rs374132769 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122437 | AGATCTCTCTGTTTA[A/G]AATTATAATCCCAAC | 23092 |
| rs374146845 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969005 | GGCGCACTCATGGCT[C/T]ATTGTAGCCTTGACC | 23092 |
| rs374147819 | snp | A/T | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007823 | CTATTTTTATGTTTG[A/T]TTGCTGTTTTAAAAA | 23092 |
| rs374150723 | in-del | -/AGAA | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967732 | TTTAGTTGGGTAAAT[-/AGAA]GGAAGGAAAGAACCC | 23092 |
| rs374163302 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977588 | TGCCTCCAGTCTTTG[C/T]GTTGAACTCAGCAGT | 23092 |
| rs374167379 | snp | A/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864786 | ACAGCCCTGTGAGGT[A/G]CATACTGTCCTCACA | 23092 |
| rs374204461 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224160 | GATTTGAAATACTAT[A/G]TGGCAAAGTTTTATA | 23092 |
| rs374220034 | in-del | -/AAAG | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225136 | ACTATTACGCTTCTC[-/AAAG]AGAGACCAACATCAT | 23092 |
| rs374237825 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157031 | ATTGACAGAAAAATA[A/G]CTCTCAGGCTATGTG | 23092 |
| rs374247135 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131830 | CATTTTTAAATGTCA[A/G]TGATAATGGTACACA | 23092 |
| rs374250788 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117542 | AGGTGTAACTCTTCC[C/T]ACCCAAAAAAAAGTT | 23092 |
| rs374253739 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150181 | CTCCTGAAGAACAAA[A/G]GACAATTGGTAAGTC | 23092 |
| rs374256508 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162057 | CTCCAGCACTTTGAC[A/T]TGCGCAATGCTGCTG | 23092 |
| rs374260119 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108892 | TGACAAGCTCTCAGC[A/G]CAAGCTCTCAGCGCT | 23092 |
| rs374263831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177652 | TACAAAATATATTTA[C/T]AGTGCTTTTCAGTTT | 23092 |
| rs374270575 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198845 | ATTCAGGGAGTACAT[A/G]TACAGGTTTGTTCCA | 23092 |
| rs374271789 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793345 | GCATGCTAGTTTGAA[A/G]TACTGATGGTGAGTC | 23092 |
| rs374294176 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813986 | TGTGGACTTGGTGGC[C/G]ACCATTACTAGTTTA | 23092 |
| rs374312772 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146813 | ATCAATTAGAGCAAT[A/G]TTAGAGGCAGGAGTT | 23092 |
| rs374320372 | snp | A/T | 6.38468e-05 | 0.00564972 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041796 | GCCTCTAATTAAATC[A/T]TCACTGTTTCTTTCC | 23092 |
| rs374324239 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925225 | GCCCTGTTGCCCACC[A/T]CCCCCATGAAGACGA | 23092 |
| rs374329772 | snp | C/G | | | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142771226 | TCCCAGCAGTGGGGC[C/G]AGAGTGCCGAGCGCG | 23092 |
| rs374335259 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883639 | GCTCCGAGTGTCCTG[C/T]CCCAGGGCATTTGCA | 23092 |
| rs374346142 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836898 | AATTATGTAACTTGC[C/T]TCAGGTCAGGTAGGG | 23092 |
| rs374354998 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923890 | TTTTTGATACGGAGT[C/T]CTGCTCTGTCGCCCA | 23092 |
| rs374372710 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891953 | GTACTTCCCAGCATA[A/G]CATCTTGCAACTCCA | 23092 |
| rs374377496 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018968 | CCAAGGGTTTTGAAT[A/G]TCTTTCCATTTATTC | 23092 |
| rs374407565 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010998 | TGCCGGTCAGCATGG[A/T]TTGCTGGTCTTAGCT | 23092 |
| rs374442123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077913 | ATATCTCCCCTCCCC[A/C]AACCCTGGTTTCCAG | 23092 |
| rs374469269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047923 | TGTTGCAGTGAGGTA[A/G]GAACCTCCTACCTCC | 23092 |
| rs374476186 | in-del | -/AGTG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778960 | AAAAAAAAAAAACTT[-/AGTG]TGTGTGTATGTGTGC | 23092 |
| rs374481274 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098606 | AGTGGGTAGACATGA[C/T]AGGAAAACAATATTC | 23092 |
| rs374485332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904672 | GTGATGGGGCCGTGC[C/T]GTTTAGGATAGCACA | 23092 |
| rs374494853 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848349 | ATCACTCCCCGGGGT[C/T]TTTTAAATTTAAGAC | 23092 |
| rs374497106 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910398 | GAGGTGATGTCTTCT[C/T]GATTGTGTAGAGGAA | 23092 |
| rs374498111 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853927 | TACTTGTTGAAGGAA[C/T]GAATGAAGCTGTGAG | 23092 |
| rs374499995 | snp | A/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869049 | GGCACAGAGAGTAAC[A/T]GGCGTCCAGGAAAGG | 23092 |
| rs374502914 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929827 | TGTGATCTCACTGTT[C/T]GCTGGTGAGCCACTA | 23092 |
| rs374512795 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913845 | AGAGAGCCGTGTGTT[G/T]TATTCCTCGAGATTT | 23092 |
| rs374525130 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200156 | CACTGAAAAAATGTT[C/T]ATCTAATTTTTTTCT | 23092 |
| rs374525169 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214138 | GGGGGCGGGGGCAAG[A/G]GGAGCACATAAATAA | 23092 |
| rs374528739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029077 | CCCTGGCAACCCTGG[C/G]GCTTCACATGATTAG | 23092 |
| rs374529703 | snp | C/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777918 | AGGCTGTGCCATGAT[C/G/T]GTACTCATACTTTAA | 23092 |
| rs374530080 | in-del | AG/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998877 | CTGCTGTCCCTTTCC[AG/T]TTCCAGTTCCTACTC | 23092 |
| rs374560679 | snp | A/G | 5.09584e-05 | 0.00504744 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885448 | TTCAATTTGTACATG[A/G]TGCTGTGGATATGTG | 23092 |
| rs374570340 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888059 | CAATAGCAACTATAA[C/T]ATAGGGAAACATTTG | 23092 |
| rs374570574 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063867 | TCGTCTCTTTTAGCA[A/T]GTATCACATTCCACC | 23092 |
| rs374583188 | in-del | -/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800403 | AGATGGAGTTTCACT[-/G]TTGTCACCCAGGATG | 23092 |
| rs374585067 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926320 | AAAATTCCAGATCCT[C/T]GTTCATGATTCTTAA | 23092 |
| rs374589834 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011205 | TGGCACTAGCCCCCA[C/T]GTCTTCCCAAGGAGG | 23092 |
| rs374590683 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946618 | AAATCAAAGATGATA[G/T]TTAAAAACACATGTT | 23092 |
| rs374593315 | snp | C/T | 0.000307953 | 0.0124049 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770949 | TCGGGGACGCGGCTC[C/T]GGGGCGGGAGGAACT | 23092 |
| rs374601979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834683 | GGGCAGCTTTCCAAA[A/C]GGACAAAGGTGGAAG | 23092 |
| rs374609393 | snp | A/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869458 | ACTCCTGACCTCATG[A/T]TCCACCCGCCTTGGC | 23092 |
| rs374611454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809022 | CCTGTATGGCTGGCT[A/G]TTCTGATTTTAAGTC | 23092 |
| rs374618820 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909129 | CCCTTTGAGTTTCGC[C/G]TCCTTCCCATTCTAT | 23092 |
| rs374629155 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951730 | TTAGGGAGTCCCCAG[A/G]CTGCTGTGGCTGTTC | 23092 |
| rs374637673 | snp | A/G | 1.66996e-05 | 0.00288956 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879481 | GGTCTGGATTTTAGG[A/G]TGAGAGGTCTGGAAA | 23092 |
| rs374639606 | snp | A/G | 0.00102717 | 0.0226391 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147416 | GCCTACCCCACAAGG[A/G]CTTTGGTCAGCCATT | 23092 |
| rs374661127 | in-del | -/CTTTT | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869189 | ACTTTCTTTTCTTTT[-/CTTTT]TCTTTTTCTTTTTTC | 23092 |
| rs374666593 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165639 | GTGTGATGTTATGAG[G/T]ACTGGGCTTCTAATG | 23092 |
| rs374671526 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964168 | GATATTAAAATATAG[C/T]CTTTTACCCTGAAGG | 23092 |
| rs374678611 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202140 | TAGTTAGCTCTTCCT[A/G]TTGCATTAAGTTAGC | 23092 |
| rs374679063 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143790 | TGCTGTATGGCCAGA[C/T]AGCATGTCCCTGCCC | 23092 |
| rs374686583 | snp | A/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016892 | CCCCTCCTTGGTGGG[A/G/T]TTGTTTTACTGTATC | 23092 |
| rs374690142 | in-del | -/TTTA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104908 | AAACATTGAATAACA[-/TTTA]GTTATTTCTGGATGG | 23092 |
| rs374698822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142771463 | GCTTGGTTAGCTTGC[G/T]ATTCCTTGGAGTATT | 23092 |
| rs374721413 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079161 | TACAAGCTTTGTCAT[G/T]TCTGAGTGCAAAGTC | 23092 |
| rs374741024 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899984 | TGAAGGATAAATCAT[A/G]GTTAATAGGAGGAAT | 23092 |
| rs374741411 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004017 | GAACAAATTTATAGA[A/C]AAAAAAAAAAAAAAA | 23092 |
| rs374747051 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021973 | TGGTGGTACACTAGG[C/T]CATTTGAGAGAGTAT | 23092 |
| rs374749733 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001529 | GTGATGGGTATATGC[A/G]TGTTTACTGTCTCTT | 23092 |
| rs374753259 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003524 | TTCCCCTAAACCCTG[C/T]CCCATAGAAATGTAA | 23092 |
| rs374754384 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829538 | TCTGCAGAGCAGAGG[A/G]CACCTCACATCACCA | 23092 |
| rs374756121 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788822 | CAGATACTAAGGGAC[A/C]ACTGCAGTAGAATAT | 23092 |
| rs374758230 | snp | C/T | 0.000347939 | 0.0131852 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885246 | GATGGAGGCTGCTTT[C/T]ATTCCTGCAACGTGT | 23092 |
| rs374764549 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210644 | TGCATTTGCCCAGGG[G/T]TCCCTGGAAATTATG | 23092 |
| rs374769210 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900615 | AGAGTAGGGGGAGGG[A/G]GGGCGGGATGAGATT | 23092 |
| rs374769373 | snp | C/G | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142770133 | GCGGGTGCACAGCAA[C/G]GCTCACCCCTAGGTT | 23092 |
| rs374781223 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849603 | TGGGCTTCTCCTCCC[C/T]AACCAGAAGGTCTGC | 23092 |
| rs374785066 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921663 | TGTATGGCAGGCTGC[A/G]TGATGCAGGTAAAAA | 23092 |
| rs374793567 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937749 | ACACAACAACCGGGT[A/G]CATCTTAGGAGCATT | 23092 |
| rs374815155 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193350 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTTA | 23092 |
| rs374823934 | in-del | -/GAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016243 | CCTCCCTCAAGAAAA[-/GAA]TAAGACAAACAGTTT | 23092 |
| rs374827734 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147710 | AAACGTCCAGGGACT[G/T]TAGCAGCTCTGTGGC | 23092 |
| rs374833151 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884909 | TGTGAGGATATCTTC[C/T]TTCCTTGGTGTTAGC | 23092 |
| rs374837620 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177056 | CTTTATATTATATGT[A/T]GGGACCATACCTCTT | 23092 |
| rs374865459 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067038 | CCCCTCCTCTGCCCC[C/T]CCCCCTCCCGCTTCT | 23092 |
| rs374875562 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215161 | TGGGCTGCGTTGCTT[C/G]GGCTTCTGCCCCCCT | 23092 |
| rs374875735 | in-del | -/TCCTCTTCCTCC | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968068 | TGCTTCTCCTCCTCT[-/TCCTCTTCCTCC]TCCTCTTCCTCCTCC | 23092 |
| rs374882750 | snp | A/G | 4.94515e-05 | 0.00497225 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142907741 | GAAGCACTACTGTAC[A/G]TATCAACGGGATTCC | 23092 |
| rs374890283 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097602 | GAGGCGGGTGGATCA[C/T]GAGGTCAAGAGATTG | 23092 |
| rs374896110 | snp | A/G | 1.67178e-05 | 0.00289113 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054421 | TGTGCTTTATGTATT[A/G]TCTTTTCTTCATTTT | 23092 |
| rs374917325 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182297 | TCTTGAACAGTTGCA[A/G]AACTCATCCACAGTT | 23092 |
| rs374932134 | snp | A/G | 3.33522e-05 | 0.0040835 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143121142 | CTAATAGAAAACCAC[A/G]AAAAGGTAATATGTA | 23092 |
| rs374947192 | in-del | C/TTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023526 | AGAAAAGAGGATTTG[C/TTT]TTCTTTTGCTTCTAG | 23092 |
| rs374949897 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022724 | ATGCTGTTCACAGCA[A/G]CTGAGTTTCCAAAGG | 23092 |
| rs374968514 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914991 | GAGGGCATGCTTTGT[C/G]TTGCAGCTCTCTGTC | 23092 |
| rs374981182 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876809 | AAAAAAAAAGGATTT[C/T]TTTAAAACTCCAAAC | 23092 |
| rs374998417 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962069 | GAGTTAATGAGAAAC[C/T]TCAAAAGCAAAGCAG | 23092 |
| rs374999866 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092760 | AGACCTCGTTCAGTC[C/T]ATATTAACTTAGAAT | 23092 |
| rs375007507 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080779 | GGGTGTGAATGGCAC[A/C]ATCTGTGGTGAGGGT | 23092 |
| rs375020461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859983 | CCCCCTTACTCAGTC[A/G]TAGATATAAGACACT | 23092 |
| rs375032447 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808063 | ATACGGTGAAACCCC[A/G]TTTCTACTAAAAATA | 23092 |
| rs375033845 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123884 | AAATGTTTTAGAACA[A/T]AAAACTTCATAGTAT | 23092 |
| rs375040500 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962582 | TTCCTTGTTTGACTA[A/G]CAGGCCTGAATGGTG | 23092 |
| rs375073477 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037182 | ACTTGACTGTCCTTC[C/T]CTTGCTCTTTCAGCT | 23092 |
| rs375078864 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228554 | AGGCTAGTGTTCAAA[A/G]GCACTCTAAAAGACA | 23092 |
| rs375079078 | in-del | -/CAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158892 | AAACAAACAAACAAA[-/CAAA]GGCAAAGGTGTTCAT | 23092 |
| rs375099352 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211898 | CCACTTCATTATTCA[A/G]TTTCACAAACCTAAT | 23092 |
| rs375115590 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060184 | CTATTGTTCCTCTGG[C/G]CTACTTACTTAATGG | 23092 |
| rs375120882 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115737 | AGCCTTTCAAGTTTA[C/T]AAGCTACAAGCTACA | 23092 |
| rs375124957 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111976 | CACACTTAGAAGAAG[A/G]TGGCCTCCCACAGCA | 23092 |
| rs375127811 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121331 | TGGTAAAGGTGTCAA[C/T]CGTGGTAGTTACAAT | 23092 |
| rs375129594 | snp | G/T | 0.0622301 | 0.165053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092165 | ATCCCTTTGTTTTTT[G/T]TTTTGTTTTTTTTTT | 23092 |
| rs375129696 | in-del | -/G | 0.0543475 | 0.155628 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111978 | CACTTAGAAGAAGGT[-/G]GCCTCCCACAGCATC | 23092 |
| rs375155146 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081602 | CGGTGAAAACAGAGG[C/T]GTCCTTGTTTATAAA | 23092 |
| rs375175852 | in-del | -/AA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096097 | ATGCAGTTACATTAA[-/AA]GATCTATTGACCTAC | 23092 |
| rs375195569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881546 | ACCATGAATAATTAT[C/T]GATTATTAAATAACT | 23092 |
| rs375203434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899697 | CTTTGTAATACTTCA[A/G]AGGTTCATATAGTGT | 23092 |
| rs375204775 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940355 | TTCAGGGGTACATGT[A/G]CAGGTTTGTTATGTA | 23092 |
| rs375210380 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883188 | TTGCCAGAATGTCCC[A/G]GAATGCCAGTGACTC | 23092 |
| rs375222839 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872971 | TGTTGTGAGTAGGAC[C/G]TAGGGGAAATTACTG | 23092 |
| rs375223082 | snp | A/G | | | intron-variant, missense | ARHGAP26 | GRCh38.p7 | 5:142919330 | TGGCAGCAGAGCACC[A/G]GAAGCTAGAGGAGAG | 23092 |
| rs375233118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864176 | AAGTTCCACCTTCTG[A/C]GGAAGCCCAGTACTT | 23092 |
| rs375237165 | snp | A/C | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007742 | TGAAATAAAATCATT[A/C]GTTTAAACGCTTAGT | 23092 |
| rs375238955 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975294 | ACTGCGTCTACAGTA[G/T]TGATTTTCAAATTAT | 23092 |
| rs375239087 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027735 | GCATAGCACTGGCAA[A/G]TAGTTGTTGTCCAGC | 23092 |
| rs375245203 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976823 | GAACCTGCTGGTTCA[A/G]ACTTTTCTGTGTTTG | 23092 |
| rs375248514 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125300 | GGGTTAATAGTGAAC[A/G]TGATCTCCTTTATTT | 23092 |
| rs375249606 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064389 | AAGGGAGTTACTTCC[C/T]TGACTGGCTCTTTTT | 23092 |
| rs375254690 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212920 | GGAGGCTGAGGCAGG[C/T]GGATCACGAGGTCAG | 23092 |
| rs375258712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046066 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 23092 |
| rs375268919 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988630 | CTTGTGGGCGTTTAG[C/T]GCTATAAGTTTCACT | 23092 |
| rs375278163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005102 | AAAAAAAAAATTACC[A/G]CAACCCTTGTCTGTG | 23092 |
| rs375282329 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108333 | ATGTTAGAGCTCTAG[C/G]ATGTTTTTCACCTTT | 23092 |
| rs375293466 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042001 | GGAATCGGGGTGTCC[A/G]TGAGCTGTCACCTAG | 23092 |
| rs375300445 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017135 | ATTCCAAATGTCCGG[C/T]ATTTTCTTTTCTAGG | 23092 |
| rs375303437 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139675 | AGCTTTAATATGCTC[A/G]GCCAAGCCACTCACG | 23092 |
| rs375313675 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219615 | GCTAAGCCTTTACAT[G/T]GAAACAGAAGACAGC | 23092 |
| rs375320297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137136 | TTCAATGGTCTCACT[A/G]TATTATTCTCTAATA | 23092 |
| rs375321623 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792626 | TGCCAAATGTAGAAA[A/T]CTCTATCCCCATTGA | 23092 |
| rs375322198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869091 | AAGGCCCGGGGACTT[C/T]GGTATTCTTGAACTT | 23092 |
| rs375325386 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143208537 | TTTCATTCTATCCTC[A/G/T]TGTGAGAATGAGAAG | 23092 |
| rs375336475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904201 | CTCACTTCAAGAGCC[A/G]AGAAGAAGGCTGCAT | 23092 |
| rs375360683 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022041 | ATGTGTATTGTGGGG[G/T]AACATAAGTTCTCTG | 23092 |
| rs375361861 | snp | A/G/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860836 | ATCTGGAGGGGTTCC[A/G/T]TTACTGGTACTTAGT | 23092 |
| rs375374546 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808002 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 23092 |
| rs375398540 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800328 | TGTCTCTGTCTCTCT[C/T]TCTCAAACTGCCATC | 23092 |
| rs375405775 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833841 | GTAAGTAATTTACCT[A/C]GTCTTTCTGAAACAA | 23092 |
| rs375408047 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777451 | AAGCAAGTTGTAAAG[C/G]GGACTTTGTTATCCT | 23092 |
| rs375421459 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799647 | GCTGGGAAGTCCAAG[A/T]TTGAGGGCCCAGCAT | 23092 |
| rs375421516 | snp | A/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861576 | GGGCGAGAGGGAGTC[A/G]AAGTGGTAGGGGCCG | 23092 |
| rs375431090 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142903609 | ATGAAGGAGAATCCC[A/C]TTGAGCACAAGACCA | 23092 |
| rs375444979 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160060 | TGAGAAAAGATTTTT[-/C]TTTTTTTTTTTTTTT | 23092 |
| rs375452520 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014185 | AGAAGTTGCTACTCC[A/G]GGTGTGAACCACCAG | 23092 |
| rs375457039 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944137 | GAGGGAGAAGTCCCT[C/T]TCTAGAGTTAAAAGT | 23092 |
| rs375468392 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843513 | GCCAGGCAAACCCAC[A/G]TGCTTTGCACATTTT | 23092 |
| rs375472194 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111199 | AATTATCCTTGTAAA[A/G]ATAATCAGGTTCTTC | 23092 |
| rs375486673 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123197 | ATAGAATATTGCCAA[A/C]GTCATGGTATTTGAC | 23092 |
| rs375492271 | snp | G/T | 0.000396484 | 0.0140743 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055990 | GAATATGATTATTCT[G/T]ATTATTAAGCTGACT | 23092 |
| rs375502594 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173929 | ATGAATTTGGTTTTG[A/G]CAAAACTAAGTAGCT | 23092 |
| rs375508832 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026107 | CTGCAGGGGCCTGAA[C/T]TCTAGAAGGTACCAA | 23092 |
| rs375533181 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022238 | TACCACACCTGGCTA[A/G]TTTTTTTTATTTTTA | 23092 |
| rs375536203 | snp | A/G | 1.6983e-05 | 0.00291397 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207524 | TATCCAAAGCTGGCC[A/G]GGGACAACAGGGGGC | 23092 |
| rs375566686 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039539 | TTAATTTTTTTTTTT[-/T]AAATTTAAAAGAAAA | 23092 |
| rs375573725 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227477 | TTTGGCAGCCACACC[A/G]ATCGGCTGGGTGCTG | 23092 |
| rs375579319 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096153 | TATGCATGATTTTTT[-/T]CTTAGCCTACATTGC | 23092 |
| rs375587451 | in-del | A/GGTCG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090455 | TACGATAGCTATCTC[A/GGTCG]GTCGTGTCATTAGAT | 23092 |
| rs375589763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210398 | TCTCTCCCACAACAC[A/G]GGAATGATGGGAGCT | 23092 |
| rs375602349 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041722 | AGGACTGAGAAAATG[-/A]AAAAAAAAAAAAAAA | 23092 |
| rs375614273 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819175 | TGCCTCAGGAGGTCA[C/T]CCTAGTCCAAGTCGA | 23092 |
| rs375616830 | in-del | -/AAG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040590 | ATCAAATAACAAACA[-/AAG]TAATTTCAGATATTG | 23092 |
| rs375624619 | snp | G/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966435 | AGAAGACAACTATTC[G/T]GTAAAAGTATGTGTA | 23092 |
| rs375633843 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786486 | AAAGTGTTTTTAGAG[A/G]TAGGATCTTGCTGTG | 23092 |
| rs375637325 | in-del | -/GAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824721 | CTCTGTGGGACTTAA[-/GAA]CATATAGGGAATGAG | 23092 |
| rs375663534 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091508 | TTCCTTTAGCACCTA[G/T]TTTTATTAGTTTCTA | 23092 |
| rs375664767 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882265 | AATAAAACTTGCCTC[A/G]TAGAGTTATTATGAA | 23092 |
| rs375686241 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958915 | CTCTTAAAAAAAAAA[A/G]AAAAGAAAAAAAAAA | 23092 |
| rs375687559 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843261 | GCTGCTGTTGCTTCC[C/T]AAGCATGCAGCTGAG | 23092 |
| rs375701591 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185070 | TACTGATGGTTGGGT[A/G]GTTTTCACACAGCCA | 23092 |
| rs375718921 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787571 | CAAGCCCACAGCTGA[A/C]AAAGCCACTGACAAA | 23092 |
| rs375724018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149225 | TGATAACAGGAACGG[C/T]TCTAATTGTCTCTGG | 23092 |
| rs375729351 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996083 | CATTAGGAGAAATAC[C/T]TAATGTAGGTGACGG | 23092 |
| rs375757201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217561 | TGAGAGGAGCTGGAT[C/T]CATTCATTCCCATGG | 23092 |
| rs375759335 | in-del | -/CTTTT | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869201 | TTTCTTTTTCTTTTT[-/CTTTT]TTCTTTTTTTTTTTT | 23092 |
| rs375762709 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957471 | GACCATAAGATATTG[A/G]TCCTCATGTTAGGGG | 23092 |
| rs375771159 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990588 | TTTCTCCCCATCTTT[G/T]TGGTTTTATCTACTT | 23092 |
| rs375771380 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010661 | TGAGTACATGTTTCT[A/G]GTGCCTTTGACTCAT | 23092 |
| rs375787576 | in-del | -/TTTAT | 0.284995 | 0.247539 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980352 | AAGCCTCTAGGAACC[-/TTTAT]TTTATTTTATTTTAT | 23092 |
| rs375792940 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877589 | AGGTCTTATTAAGGC[C/T]GATAGCAAGTAGTAG | 23092 |
| rs375793614 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055100 | AGGTTGGGTTATTGA[C/G]CAGCTGCCTGCATCT | 23092 |
| rs375809110 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858961 | GGCCGGATGGATTGC[G/T]GCACCTTTGATTATC | 23092 |
| rs375810445 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845600 | GCTGAACTGCAGACC[C/T]GTGTATTTTTAGAAA | 23092 |
| rs375819159 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989769 | TCTTTTCTTTAAGAA[C/T]GTTGAATATTGGCCC | 23092 |
| rs375836819 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917599 | CCCGTGACTAAATTA[A/G]AAGAAGCAATGCAGA | 23092 |
| rs375841003 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204502 | GCACTCCAGCCTGGG[C/T]GACAAGAGCAAAACT | 23092 |
| rs375846231 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174775 | GCAATATGGGATTAC[A/G]TAGGATCATAGGTAA | 23092 |
| rs375857719 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100935 | TCTCTACTAAAAAAA[-/A]TTGAAAAACTAGCTG | 23092 |
| rs375858021 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059142 | TCTTAGTTGCAAAAC[-/TT]TGCACACTTGAAGGA | 23092 |
| rs375858341 | in-del | -/AGGCTGTTTGGTTGCCTTGGAGTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168684 | TTCAGCTTTTAGCAA[-/AGGCTGTTTGGTTGCCTTGGAGTT]AGGCTATATCTCTAG | 23092 |
| rs375863338 | in-del | -/AAGAAT | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163129 | AAAAAGAAAAAGAAA[-/AAGAAT]AAGACACTATTCGAG | 23092 |
| rs375863670 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012740 | CTCACTGCAAGCTCG[A/T]CCTCCTGGGTTCATG | 23092 |
| rs375884155 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780241 | AAATATAGTGTATGT[A/G]ACCATTCCCCTAATA | 23092 |
| rs375900899 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821507 | GTAACCCTGAAAAGA[C/T]ACCTTACAGCAAGGG | 23092 |
| rs375901098 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805188 | GCTCACTGCAACCTC[C/T]GCCTCTCGGGTTCAA | 23092 |
| rs375909507 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838774 | ACTTTGGAAAAAGAG[A/G]CAGCTTTGGAATTAT | 23092 |
| rs375917603 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775652 | CTTTCCCCTCCCCCA[A/G]CCCTAGTAACCTCTA | 23092 |
| rs375945132 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936414 | AGAGACATTAATGGG[G/T]TGGAAAAATCAACAT | 23092 |
| rs375954705 | snp | A/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860292 | AATGCCCATGAAGCC[A/G]CCCTGCCTATACCTT | 23092 |
| rs375957232 | snp | A/C/G | 0.000428556 | 0.0146327 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214129 | ATATGGGCGGGGGGC[A/C/G]GGGGCAAGGGGAGCA | 23092 |
| rs375967427 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893427 | GTTCCATTCATGTTG[C/T]TGCAGATGACAGAAT | 23092 |
| rs375977244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104679 | CTGACTGTCCAATAA[C/T]GGGAGATTTCTAAAT | 23092 |
| rs375988873 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851228 | CAGCCTCCCGAGTAG[C/T]TGGGATTACAGATGT | 23092 |
| rs375993828 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134733 | TTGCAATGATCAGGT[A/G]CTGACCCCTAAAATA | 23092 |
| rs375994805 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142913239 | AATCCTGCACACGGC[A/G]GAAAACAGACTCCAT | 23092 |
| rs375997410 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805705 | CCAGAACCCAGAAAG[A/G]TGAGCTGGACAGATT | 23092 |
| rs376006611 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773511 | AATGAGATGCTGGCA[A/G]TGGAGATGCAAATTC | 23092 |
| rs376013019 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823476 | TCTCCCATTGTCCAC[C/T]CTAAAGCCTGGCTCT | 23092 |
| rs376062186 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997765 | TACTTTTTTTTTTTT[-/T]CATTTTGTGGTTTCT | 23092 |
| rs376062590 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829922 | CACAGCTAGGAAGTG[A/G]CAGAGGTTAGGTTTA | 23092 |
| rs376070473 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151275 | ACTGACAACATCAAA[C/T]GCTGGCTAGGATGTG | 23092 |
| rs376074209 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976267 | CTGTTTGAAATAGGA[A/G]TATGAAACCATTTAG | 23092 |
| rs376077455 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101939 | ATGGCAACAGGTTCT[A/G]TTTTCCTTAGGGGCT | 23092 |
| rs376077729 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889966 | GTGGAGAAACCCCCA[C/T]CTCTATTAAAAATAC | 23092 |
| rs376080954 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164495 | CACAAGCAAGTGCCC[A/T]GGTTCATCATTTCAA | 23092 |
| rs376086374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802191 | ATCATTGGTGATGAA[A/G]GCTATAAACAGATGT | 23092 |
| rs376115007 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038025 | AGAGACAGCCACAAA[A/G]GAGATTCCTCAGTCC | 23092 |
| rs376115682 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905391 | GATGGGGATACAGCA[A/C]TTTTTTTTTAATTTT | 23092 |
| rs376139816 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079298 | CTACTGTGAAGTAAG[C/T]GCTTTCTCCTTTGGA | 23092 |
| rs376146248 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856225 | GGGCACACAGTGGGG[G/T]CCAGCCTGGGCCATG | 23092 |
| rs376148773 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875844 | CTCCTGGGCTCAAGC[A/G]ATCCTCCTGCTTCAG | 23092 |
| rs376148837 | in-del | -/TC | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915928 | AAGACTCCTGTACTT[-/TC]CTTTTTCACCAATGT | 23092 |
| rs376149846 | snp | G/T | 0.000137365 | 0.00828635 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207177 | TGTGCTGACAAGTTT[G/T]CTGGTTGTTATGTCT | 23092 |
| rs376152131 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989214 | GGATAATTAGCTCTT[C/T]TTGTTGAATTGATCC | 23092 |
| rs376153891 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910202 | TTTTCCTCCTTTTAC[A/G]AAGGAGGACATTGAG | 23092 |
| rs376156023 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098894 | AAATATTTTTTAAAC[A/C]TGACTTTGTGAAAGT | 23092 |
| rs376160163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142972130 | GAGGTTGCAGTGAGC[C/T]GAAATTGTGCCACTG | 23092 |
| rs376162127 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841764 | AGATGGCTGGCGGAA[C/G]AGGGTAGAGACAAGG | 23092 |
| rs376165435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955519 | AAAAATCCAGTGAAT[A/G]CTGTGGACTCTCTAA | 23092 |
| rs376166353 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089495 | TGTTATACTTCCATC[A/G]GGGGTGGTGGTGTTT | 23092 |
| rs376170702 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020726 | TCACTGCAAGCTCCC[C/G]CTCCCGGGTTCACGC | 23092 |
| rs376170795 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873383 | ATTCCTGATTTTTCC[C/T]GTCTTTTTCTTGCTA | 23092 |
| rs376173806 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003820 | ATGAGAAAGCAGACT[C/T]GGAAATGTTGAATGA | 23092 |
| rs376178538 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047566 | TATTCCCAAGTGTGT[A/T]GTTAGCAAAGTCTGA | 23092 |
| rs376186160 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172252 | AACTGTCCTCTGAGC[A/G]TGGTTGATAACCAAA | 23092 |
| rs376189876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161284 | CCCAAAGTGCAGGGA[C/T]TACAGGCATGAGCCA | 23092 |
| rs376214561 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849193 | TTGAAAGATTGAAAC[A/C]ATCTCAGGATAATTT | 23092 |
| rs376216546 | snp | A/C | 1.65679e-05 | 0.00287814 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901920 | GTGACCTTTGCCTTT[A/C]TTCCTTCATTACAGC | 23092 |
| rs376238111 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995781 | TGCTCATCAATGATA[C/G]ACTGGATGAAGAAAA | 23092 |
| rs376243146 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975433 | ATTCAATTTTTATCT[C/G]TCTGTCTATTTTTGA | 23092 |
| rs376245524 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182817 | TTCTCAAAATCAAGC[C/T]CCATGTAAATAGTCA | 23092 |
| rs376246517 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928548 | GTGAGCTCTCTGGGG[A/G]CTGCGGTGCCATCAC | 23092 |
| rs376249409 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997989 | CTTTGGACAGAAATA[C/T]ACATAAAATAGGATT | 23092 |
| rs376253755 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041716 | TTTTAGGAGGACTGA[A/G]AAAATGAAAAAAAAA | 23092 |
| rs376254695 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216019 | GTTTAAGTGTTTGAG[A/G]AAATGCCGAACTGTT | 23092 |
| rs376276848 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887161 | CAGATCCATTCTCTC[C/T]GTGGTCAAATATTGC | 23092 |
| rs376280436 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160473 | AGTTGTTGCTTTTGG[G/T]GGTTTTTTTTTCTTT | 23092 |
| rs376289042 | snp | A/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861620 | TCCTTTCATTTTTAC[A/G]CAGAAACAAATCAGC | 23092 |
| rs376293738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792968 | CATCGAAGGCAGAAA[A/G]GTTGGAGGAACTTTG | 23092 |
| rs376307859 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972700 | GAAATCCTGAATGCA[A/G]TACACATTATTAACT | 23092 |
| rs376313276 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862834 | ATGGTACACGTCACC[C/G/T]TCTTAATCTAATTGA | 23092 |
| rs376316606 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994513 | CATGAAGGGTATGCA[A/G]TTTTTGGGAAGGCAG | 23092 |
| rs376323436 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167355 | GGCCTGATGGCATGC[A/G]CCTGTAATCCCAGCT | 23092 |
| rs376345221 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016040 | GGTGATAATAGCAAA[A/G]AATGAGAGACAATCT | 23092 |
| rs376349120 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088074 | ACTTCTAAAAGGTCT[C/G]ACATAAAGCTGGTGC | 23092 |
| rs376354527 | snp | A/C/G | 7.68128e-05 | 0.00619688 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873544 | CATTGTTTGTCATAG[A/C/G]CTTCAGTGTCCCAGC | 23092 |
| rs376364477 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050345 | TTTTTTGTTCTTCTT[C/T]TTCTTTTTTTTTTTT | 23092 |
| rs376373531 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993733 | TGCAGCCCCAACCTC[C/T]TGGGGTCAAGCTATC | 23092 |
| rs376382759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092054 | TTACTTTTAAATTAT[A/G]CAATATTTCTTGCAT | 23092 |
| rs376382957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123035 | AAGCAGGGACGTTGT[A/G]TTTTGTTCCTCAGTA | 23092 |
| rs376395047 | snp | C/G | 0.000153988 | 0.00877328 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222449 | GGAGTTCCTCTAACC[C/G]TGGGCCCCAGCAGAA | 23092 |
| rs376417101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054607 | TTTATTTTCAGACTC[C/T]GGAGAGCTGTCGGGT | 23092 |
| rs376422593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890077 | GGAGGCGGAGGTTGC[A/G]GTGAGCCGAATTCGC | 23092 |
| rs376440073 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929571 | TCCGTCCCCTACCCC[A/G]CTTCCCCTGTAAAAG | 23092 |
| rs376452373 | snp | G/T | 0.0498117 | 0.149749 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986285 | TTTTTTCATGTGTCT[G/T]TTGGCTGCATAAATG | 23092 |
| rs376459290 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148630 | TGGACCAGTGCCTCA[A/G]GACCTCAAAATAATT | 23092 |
| rs376467831 | snp | A/G/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078880 | CTGACTGGTGAAACC[A/G/T]GTGGTTATGGTAGCA | 23092 |
| rs376468412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161364 | GAAACCAGAAAGTCA[A/G]TGTTAACATTGAGCA | 23092 |
| rs376468969 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169060 | ACTACTAAAGTGACT[G/T]TTGGGGCCTTTGCTT | 23092 |
| rs376476411 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884577 | CAGCAAGTTTATATA[A/C]TGCTGTTTTACTTTT | 23092 |
| rs376484081 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226960 | AGTTTCTATCAGCTG[A/C]AAATGGCAACTGCTG | 23092 |
| rs376495796 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814830 | CACTGGTTGTTGTGA[C/T]AATCAGATGAGATAA | 23092 |
| rs376508214 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128656 | GCACCACGCAGTCCT[C/T]GGTCCCATTGTCTGT | 23092 |
| rs376510515 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103494 | AAAGACACATGCACA[C/T]GTATGTTTATTGCAG | 23092 |
| rs376512596 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065773 | TCCCACCCTAGGGAG[A/G]CATGACACAAAATGG | 23092 |
| rs376522081 | in-del | -/GA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858043 | GGAGAGAGAAGGAAT[-/GA]GAGAGAGAGAGAGAA | 23092 |
| rs376534474 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906288 | CTAATTAGCAATCTG[A/T]AGGTAACACCTTAAG | 23092 |
| rs376544462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079403 | TTGCTACCAGGCTAC[A/G]ATTCTTTGGTCTTTG | 23092 |
| rs376554053 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855381 | GAGATGAAATGAAGT[A/G]GAGGTTTTAGAGGTG | 23092 |
| rs376554833 | snp | A/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041037 | GGAATAAAATAGGAA[A/G/T]CTGGAGCTCTATTAC | 23092 |
| rs376564007 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053988 | CTTAATCATTCTTCT[A/G]TCGTTGGACATTTAG | 23092 |
| rs376564201 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082974 | ATATCATATTCTTTA[A/T]GCAAAGATTGTCACT | 23092 |
| rs376582062 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108793 | TCCCATGAACCCTTC[G/T]GTGGATTTGGAATCT | 23092 |
| rs376585342 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139909 | AAGGATTGAAGGGAG[C/T]CAGCAACAAGGTCTT | 23092 |
| rs376586326 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841025 | TATAACAGGTTATTT[A/G]GGGAAATTAGTAATA | 23092 |
| rs376597728 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171346 | CAACAAGTCATCCAT[C/T]GTCTTGAGGGCTAGT | 23092 |
| rs376608396 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820130 | TGGAAATGGAATCCA[C/T]GAATGTGCATTTCAC | 23092 |
| rs376615311 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200790 | TACTCCTCCAGTTAC[A/G]GAACCTCTCATCTTA | 23092 |
| rs376618545 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945846 | CAAGTCTTAAATTTT[A/G]CCAGTTATCTCACTA | 23092 |
| rs376619074 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097715 | TAGTCCCAGCTACTC[A/C/G]GGAGGCTGAGGCAGG | 23092 |
| rs376633578 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046281 | TGAACTCCAGCCTGA[A/G]TGACAGAGCAAGACT | 23092 |
| rs376639411 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197541 | TCCCTATTCAGGTTT[C/T]TTGCCCATTTCCCAC | 23092 |
| rs376642506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874851 | CATCTCACCAGTCCT[A/G]GATACTCTCAGGAAC | 23092 |
| rs376647719 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805334 | CTCGAAGTCCTGACC[A/G]CAGGTGAACCACCCG | 23092 |
| rs376659086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845333 | GGTGGGTATTTGTTA[C/T]CACCCTGCTTCACAG | 23092 |
| rs376672950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971190 | AAAATAACCGAAGTT[A/T]TAACTGTTTCTCCTT | 23092 |
| rs376674038 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835047 | CTGGGGCTAGTAGGG[A/G]ATGTATTGTCTCCAT | 23092 |
| rs376680668 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946469 | CTTTGTGGGAAATGC[A/C]ATTTGCAAAAGAAAG | 23092 |
| rs376682489 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050827 | GGAGCTAGCAATACG[A/G]CTACTAATCACAATC | 23092 |
| rs376688331 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092552 | AAATTCTCCCCCCCC[-/C]ACCTTTTTTTTTCTC | 23092 |
| rs376688797 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016617 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGAGAG | 23092 |
| rs376693094 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777609 | TTTCAAATTATATAT[A/T]TTTTGCCATCAGAAG | 23092 |
| rs376693987 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035697 | TCCCAGCATTTTGGG[A/G]GGCCGAGGCGGGTAG | 23092 |
| rs376700072 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070525 | AAACAAATGGAAAGA[C/T]ACCCCATGCTCATGG | 23092 |
| rs376717812 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071873 | TTGCTCCACTGCACT[C/G]CAGCCTGGGCAACAG | 23092 |
| rs376720332 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101865 | TAAAAGCTTTTTTTT[C/T]TTTTTTCTTCCATAA | 23092 |
| rs376728752 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773099 | TGACCTCTAAAAATA[A/G]AGGGTGGAGTCAACC | 23092 |
| rs376736290 | in-del | -/CTGCTTCC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212335 | AGTCACTCCTCCTGT[-/CTGCTTCC]CAGCCTCTCAAGAAA | 23092 |
| rs376744336 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182732 | AGACAAATCCCTTGC[C/T]CTATGTGTGTGGTGG | 23092 |
| rs376748516 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156938 | CAAGACAGGGTGGGT[A/G]CATCAATTAATCAAG | 23092 |
| rs376754941 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029698 | ACAGTTGAGAGCCAG[G/T]GTGCTCAACCTCAAT | 23092 |
| rs376755516 | snp | A/C | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192199 | TCCAAGGAGAAAGAT[A/C]TAACTCACTGGAGAA | 23092 |
| rs376762063 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007548 | AGGCTGTTTTTCCTC[C/T]GGAAAGCAGGACTGG | 23092 |
| rs376773182 | snp | A/C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864136 | TCCCCTTTCTAGAAA[A/C/T]GTGTCTACCTTAGGG | 23092 |
| rs376788555 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790323 | ACCACAGTGTTGAAA[A/G]TTGTAAGGCATCCCT | 23092 |
| rs376789157 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824719 | GTCTCTGTGGGACTT[A/C]AGAACATATAGGGAA | 23092 |
| rs376793599 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975430 | CACATTCAATTTTTA[C/T]CTGTCTGTCTATTTT | 23092 |
| rs376796710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220584 | TTAAGAGTGGCATGG[A/G]AGAGCTTTGGTCATT | 23092 |
| rs376804530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859308 | TTGAGGTTGTAAAGC[A/G]ATCCCAGGGTATTCC | 23092 |
| rs376808061 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853482 | AGACGTGAGCCACTA[C/T]GCCCAGCCTAGCTTA | 23092 |
| rs376810931 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184572 | GATGGACTGGGGGAA[G/T]CCAGTAATTCTTAAT | 23092 |
| rs376826145 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820820 | GTATGCATTTTCTTA[G/T]TTTTCCCGGAACATT | 23092 |
| rs376834619 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226684 | GAGCCAGTCTTTAGC[G/T]TAATGTCTGAAGTAT | 23092 |
| rs376838419 | snp | A/G | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967752 | GAAGGAAAGAACCCA[A/G]TTTGTTAGAGAACAG | 23092 |
| rs376875132 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070766 | AATACAAAAATTAGC[C/T]GGGCATGGTGGTGTG | 23092 |
| rs376876825 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858060 | GAGAGAGAGAGAGAA[C/T]CTGTGTGTGTGTGTG | 23092 |
| rs376878360 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150987 | TGAAAAGACAAGCCA[C/T]ACACTAGGAGAAAAT | 23092 |
| rs376886869 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086780 | TGAGTCTTCCCTCTC[A/G]CTCAGGGGTCTTATT | 23092 |
| rs376897396 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131587 | TTGAAACACATCCTT[A/G]TATGTTTGGGACACC | 23092 |
| rs376900160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826391 | GAATTGTCATACTAC[C/T]CATTTTGCAGAGCAG | 23092 |
| rs376904217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168536 | TCACACAAGATCTTA[C/T]GACATTCTGCATCAT | 23092 |
| rs376919956 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788322 | TCAGTTCTTTTAAAA[C/G]CAGCTCCCATTTCTC | 23092 |
| rs376937550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817951 | CAGCTTTGTTGTCTT[C/T]TCTGAGCTTTAGGTT | 23092 |
| rs376940620 | snp | C/T | | | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143058248 | CCCATCTGTCTAATA[C/T]GGATAATAGACTCCC | 23092 |
| rs376975296 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831836 | TGATGATTCCTTCTT[A/G]CATTTGCTTTTTCCT | 23092 |
| rs376981486 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971043 | ATTTTTTAGGTGGCA[C/T]TGGAGGTTTGAGTTT | 23092 |
| rs376981664 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873029 | ACTGACTGTGTGGAG[A/G]GTCAGTGGCAGAGCA | 23092 |
| rs376984414 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953259 | AGTGAATATTTATTG[C/G]GTATAAACTCTGTAC | 23092 |
| rs376984547 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891257 | CCTTCTGAAACCTGT[C/G]TCCAAGTAAAGATTC | 23092 |
| rs376988920 | in-del | -/TCCCTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950962 | CTTTCCCTTTCCCTT[-/TCCCTT]CCTCTTTCCCTTTCC | 23092 |
| rs376995737 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977418 | ATCAATTAACCTTAT[C/T]AAAAAAAAAACAACA | 23092 |
| rs376997471 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927030 | TTCTTTAAAACATAG[A/G]TAATAAGAGTAGCAC | 23092 |
| rs376997852 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176331 | ATATTTATGAACTGA[C/T]GTTCACTTCTTAGAT | 23092 |
| rs376999860 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014602 | GTGGGAGGAAAGAAT[A/G]GAGATGAATTCTATG | 23092 |
| rs377011577 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049581 | TCTGTATTTTTTGCC[A/G]ACAAATATTTTATAG | 23092 |
| rs377030215 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113622 | CCATCATATTTAAGG[A/G]TAGTTCATCATTTTC | 23092 |
| rs377038692 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814264 | TGGCTAGAGCCTTCC[A/G]GTAATCTGCAACTTC | 23092 |
| rs377042888 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107787 | AGTTGGTTTGCTCAC[C/T]TTGGATCTCTGGTTT | 23092 |
| rs377049836 | snp | G/T | 0.000169334 | 0.0091999 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894229 | TCTTAAATTCCATCT[G/T]GTTTGTAGGCAGACA | 23092 |
| rs377071683 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845983 | TTTTTCCCCTGTGAG[A/T]CCAATCACGTTTTGA | 23092 |
| rs377082425 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973312 | TGTGCAGTATTTTCT[A/G]TGTGATGCAGGTCTG | 23092 |
| rs377082584 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981081 | TTGCAAATGTATCCT[G/T]TTTATAAAGGTGATT | 23092 |
| rs377085067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143199587 | GGGGCAAAATCAAAG[C/T]CGCCCCCTGTTAGTT | 23092 |
| rs377086577 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816829 | TGAGCAGAGGGTTAG[A/T]GTGATCAGCACTGTG | 23092 |
| rs377095395 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043370 | ATTTTTGCTGTTCCA[C/T]GTATTAATAGTTCTT | 23092 |
| rs377104279 | in-del | -/GC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793251 | TTGTTATATCCCTTT[-/GC]TTTTTTTTTTTTTTT | 23092 |
| rs377107959 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079689 | CTCAATGACTCCTTG[A/G]GATATTGTTATGTGT | 23092 |
| rs377114285 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855139 | TGCATTTTGGCAAGA[A/G]TGAAGTCACCGTTTT | 23092 |
| rs377130735 | snp | A/C | 0.000103239 | 0.00718392 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894394 | CCCATATATTCATCC[A/C]TCATTCTAACTAGTA | 23092 |
| rs377147244 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774694 | CATAGTAACATACAG[A/G]ATACTTTCACTACCC | 23092 |
| rs377159524 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801754 | GTACCCAACTGTTTT[C/T]CTTGCAAGGAATAGG | 23092 |
| rs377164844 | snp | A/G | 0.000301422 | 0.0122727 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907670 | AGCATACAGTGGAAT[A/G]TATAGATATTTTATG | 23092 |
| rs377166503 | in-del | -/AC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180371 | CCTCGTGATCTGCCC[-/AC]CTCAGCCTCCCAAAG | 23092 |
| rs377169812 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933191 | TGGGCACAATAGCTA[C/T]TTGATGTCAAAGGCC | 23092 |
| rs377198088 | snp | A/C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780436 | GTTTCTGAAAAGTTC[A/C/T]AAGTGAACTGAATTT | 23092 |
| rs377206760 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817317 | GGGACAGTGGCGAGT[A/G]CCACCTTCACAGAGT | 23092 |
| rs377214532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094350 | TGGTCAGTTTCTTTT[C/T]TCCCTCGCGTTGCTG | 23092 |
| rs377230126 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869474 | TCCACCCGCCTTGGC[C/T]TCCCGGAACTGTAAT | 23092 |
| rs377231100 | snp | A/C/T | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964549 | TCTGTTTAAAACACA[A/C/T]ACACACACACACACA | 23092 |
| rs377233066 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888167 | ATAGATGTGGTTACT[A/G]CTCTGTTTTACACAT | 23092 |
| rs377261346 | snp | A/G | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861482 | GTGGTATTAGTGGCA[A/G]GGAGTGTCTGAGCTG | 23092 |
| rs377280411 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928219 | ATGATTAGGACTTTT[-/TG]TGTGTGTGTGTGTTT | 23092 |
| rs377294854 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109735 | GCAAGCCGCCACACC[C/T]GGCCATATCTCTCTC | 23092 |
| rs377299653 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894370 | AGATATTCAGGGTTT[A/C]ATGATGTACCCATAT | 23092 |
| rs377304906 | snp | C/T | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965454 | AGACGCTGGCATCAC[C/T]GCTAGACCAAGGAGC | 23092 |
| rs377307154 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012339 | GATGCCCAGAGAGGC[C/T]AAGAGACCCAGTGAC | 23092 |
| rs377314651 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112531 | GTACAGTTCAGTGGT[A/G]GTGTATAGTCACCAA | 23092 |
| rs377329657 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949221 | AGAGAGAGAGAGAGA[-/G]GAGAGAGAGAGGAGA | 23092 |
| rs377332962 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085068 | AAAAAAAAAAAAAAA[A/G]AAACGCTTTCTGCAC | 23092 |
| rs377334856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140848 | TTTTTAGTTCCGTTA[A/G]TTCATCCTAGACCCT | 23092 |
| rs377337724 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944620 | TATCTTGTTTTCATT[G/T]GTGTTTCTCAGATTA | 23092 |
| rs377340244 | snp | A/G | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967267 | GAACTCTGGTTGTAT[A/G]GAGAAGTCAGATATA | 23092 |
| rs377341924 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172020 | GACTTTACAGTGTGG[G/T]TGTTATGTCCATCTC | 23092 |
| rs377344730 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777751 | TAGCGGGGAGATTGA[A/G]TGGGATGTTTGGGGG | 23092 |
| rs377349599 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999169 | GAAGAGGTTTGATCC[A/G]GGTCCCACAGTAAGG | 23092 |
| rs377352635 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924069 | GGGTTTCACCGTGTT[A/G]GCCAGGATGGTCTCG | 23092 |
| rs377353288 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081355 | GTATTCTAGTCAGGA[C/T]TCACACCATAGAGAA | 23092 |
| rs377356408 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944850 | GTACAAACCTAAGTT[C/T]CGCTTGTGTTCTTTC | 23092 |
| rs377356717 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939903 | TCTTTTTGGAGAGGA[A/G]GATGGATATTGGGAT | 23092 |
| rs377357646 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121335 | AAAGGTGTCAACCGT[G/T]GTAGTTACAATGACA | 23092 |
| rs377358994 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846411 | TCCCAGGGGAATGTC[G/T]TTTGGTGTGGCCCAG | 23092 |
| rs377359847 | snp | C/T | 1.71652e-05 | 0.00292955 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873507 | ATAGGTAAGTCATAA[C/T]TGTGCAGAAGATAAA | 23092 |
| rs377361812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096223 | TCCAATGCAAACATA[G/T]TACATCATATAACAT | 23092 |
| rs377365899 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879753 | TTATTATAATAGATA[C/G]CTGTGTGCTTAGACA | 23092 |
| rs377372510 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041965 | TCACCAGGTCTGTGA[A/G]TAGATACAGCCTGTG | 23092 |
| rs377375478 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221617 | CTGCTGAGCCCAAGC[A/G]ATCCTCCCGCTTCGG | 23092 |
| rs377438019 | in-del | -/GTT | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980964 | GTAGTTGTCATTGTC[-/GTT]GTAGTGTCACACTTG | 23092 |
| rs377443500 | snp | A/G | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769874 | TAATTTTAAGATGCA[A/G]ATAACATTTTTCTGC | 23092 |
| rs377453611 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902911 | TGACAGAGTGAGGGC[A/G]CCTGGACTCGCAGAG | 23092 |
| rs377454590 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945437 | CCATTTTTGTGGCCT[A/C]GGTTAACTACTGCCC | 23092 |
| rs377477823 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041142 | CTTCTTTTGTAAATG[G/T]TACAGTGGTGATCTA | 23092 |
| rs377478378 | snp | A/G | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769269 | CCAACCCAAACAAAC[A/G]TGAAGCCCCCACGTA | 23092 |
| rs377478685 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024023 | TACACCTCACTTTTC[A/T]TTATGAGTTGCCTGT | 23092 |
| rs377488335 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041721 | GGAGGACTGAGAAAA[-/T]GAAAAAAAAAAAAAA | 23092 |
| rs377494894 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880222 | GCTCCTTTGCCCTGT[A/C]ATAAATCACTAGGAG | 23092 |
| rs377507621 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939518 | CTAACCCCCTAGTCC[A/T]TCTAGAACTCCTGGA | 23092 |
| rs377509479 | snp | C/G/T | 6.63563e-05 | 0.00575972 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057623 | CTGATAAGATATTAC[C/G/T]TCCCTCCTTCCTTTG | 23092 |
| rs377532930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811141 | GAAGTAAAAATAGAC[C/G]TACCTCCTGGGGTTA | 23092 |
| rs377538701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215154 | ACCAGAATGGGCTGC[A/G]TTGCTTGGGCTTCTG | 23092 |
| rs377539147 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169734 | GCACACGGACTCTGC[A/G]GATGGAGAAGGGGTG | 23092 |
| rs377547857 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169461 | TAGATAAGCTCTTTC[C/G]TTTTGATTGCAGGGT | 23092 |
| rs377561199 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043146 | AAGATGCAGAACACT[A/T]CCATCACTAAAAGGA | 23092 |
| rs377567921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995490 | CCAGTTAGAATGGCA[A/G]TCATTAAAAAGTCAG | 23092 |
| rs377569917 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010113 | TGTAGAAGAAGGATA[G/T]CCCAGAGCAGACTGA | 23092 |
| rs377575992 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981873 | ACCTCAAAAGTTCCC[A/G]ACTCAGTGAAAGGCT | 23092 |
| rs377599992 | in-del | -/GG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921362 | TATGTGCATATGGCT[-/GG]GTTCAATTTTATTTT | 23092 |
| rs377608762 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202123 | TACATATATATTTAG[C/G]ATAGTTAGCTCTTCC | 23092 |
| rs377614303 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214222 | AAAAAGTGTGTGTGC[A/G]TCTGTGTGTGTTGGT | 23092 |
| rs377640846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132216 | TGGAGCCCGAGGACC[C/T]GCCAACCCATGGAGA | 23092 |
| rs377641928 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083644 | GCTGTGATTACAGGC[A/C]CCTGCCACTACACCC | 23092 |
| rs377646578 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126184 | GCATTGGGCTCTGAC[A/G]GATCAATGGAAGTTT | 23092 |
| rs377648714 | in-del | -/AGGC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114919 | GAGAACTTGCTGGGC[-/AGGC]TAGGGGCATGATGTT | 23092 |
| rs377676515 | in-del | -/TG | | | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058496 | GCATTCATCACTACT[-/TG]TGTGTGTGTTCTAAC | 23092 |
| rs377684242 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048670 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 23092 |
| rs377704126 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157131 | GGTACAGGAAGGGAA[G/T]GGGGCAAGAGCTGCT | 23092 |
| rs377708056 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192697 | TTGGAATGAGGAAAC[C/T]CAGCTAGCTTAAGGG | 23092 |
| rs377710929 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825431 | TGCACATGGGGCTGA[A/G]GTTATGGAGATGAGA | 23092 |
| rs377715307 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777967 | TGTGTAGAGACCAAG[C/T]GTAGTGGAGCAACAA | 23092 |
| rs377724690 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846873 | TAACTCTCCCTTAAA[G/T]GAGGATACCATGGGG | 23092 |
| rs377737458 | snp | A/G | 0.000447861 | 0.0149576 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041900 | TGATGGGTGAGTGCC[A/G]CAGTGGCTCTGCTAG | 23092 |
| rs377753822 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884252 | GGCTTTGGAGGCACA[G/T]TGTCCTAGGCTCCAA | 23092 |
| rs377757491 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796898 | TCTCAACACACAGAG[A/G]GTGTGGACTTAGGGA | 23092 |
| rs377758858 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194675 | GGACAAGAACTAGAA[A/G]AGAATATAAAAATGA | 23092 |
| rs386405160 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923092 | TGTCATGGAGTTTTT[-/T]TTTTTTCTTTTAATT | 23092 |
| rs386405162 | in-del | -/AA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097836 | AAAAAAAAAAAAAAA[-/AA]AGAAAATTACCCCAC | 23092 |
| rs386405163 | in-del | -/CACA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123972 | AATAGAAACACACAC[-/CACA]ACACACACACAAACA | 23092 |
| rs386693026 | multinucleotide-polymorphism | CTG/TTA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809713 | TAACTTCTGCCAGTC[CTG/TTA]CTGGAGCCATCCACT | 23092 |
| rs386693027 | in-del | G/TCAAGACCAGTCTGGAGGCA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876572 | CTTGAGCCTGGGAGT[G/TCAAGACCAGTCTGGAGGCA]ACATAGTGAGACCCC | 23092 |
| rs386693028 | multinucleotide-polymorphism | GAA/TAG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889373 | ATCCCAGCACTTTGG[GAA/TAG]GCCAAGGCGGGTGGA | 23092 |
| rs386693029 | in-del | ATC/GT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891611 | CTAAGCTCTTAAGAT[ATC/GT]CAAGTAGCATATTGT | 23092 |
| rs386693030 | multinucleotide-polymorphism | ATG/CTA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899964 | GAGGCTCTGTTTACT[ATG/CTA]AGTGAAGGATAAATC | 23092 |
| rs386693031 | in-del | AACATAA/TACCACTC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900314 | TGACTCCATGGGGCT[AACATAA/TACCACTC]ATTCACGGATTTATG | 23092 |
| rs386693032 | in-del | CATC/TGGAGGTTACATAGTAGTCAGTGTTGTCTCAGAGAACAGGA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902718 | TGGGTTTTAGAAGCC[lengthTooLong]AGTTGCAGAATCTTG | 23092 |
| rs386693033 | multinucleotide-polymorphism | AG/GC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916080 | ATGTGGAAGTGAAAG[AG/GC]GGGATGGTTATATTT | 23092 |
| rs386693034 | multinucleotide-polymorphism | GG/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921558 | GGAAAACTGAAGATT[GG/TT]TGAAAGTCAGAATAG | 23092 |
| rs386693035 | multinucleotide-polymorphism | CG/TA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931334 | AGTCTCTTTTTCTTG[CG/TA]GAGTACCATTTGTGA | 23092 |
| rs386693036 | in-del | AA/TATT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943898 | GCTTAACCTTTGGGG[AA/TATT]TAGGATTAGTTGTGA | 23092 |
| rs386693037 | multinucleotide-polymorphism | CGC/TGT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951946 | GTGTTGGCAGGGCCA[CGC/TGT]TCCCTCCAGGGAAGA | 23092 |
| rs386693038 | multinucleotide-polymorphism | CT/TC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955770 | GAAATAGACAAATGA[CT/TC]GGTTCCAGATGTTAG | 23092 |
| rs386693039 | in-del | CT/TTAAG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973718 | GGTCTGTTACATACC[CT/TTAAG]ACCCAGGACATTTCT | 23092 |
| rs386693040 | multinucleotide-polymorphism | GC/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984539 | AAGAAACAGATCTGT[GC/TT]ATTCATCTCTCAGTG | 23092 |
| rs386693041 | multinucleotide-polymorphism | CAT/TAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001007 | TATGTAACAAACCTG[CAT/TAC]GTTCTGCACATGTAT | 23092 |
| rs386693042 | multinucleotide-polymorphism | GA/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026991 | GTGGTGTGTGAATTG[GA/TT]TATAGGGTGTGAGAG | 23092 |
| rs386693043 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036665 | CATGTATTGGCTCTG[CA/TG]TCTTTGGTCAAGATA | 23092 |
| rs386693044 | in-del | CA/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040589 | TAATCAAATAACAAA[CA/G]TAATTTCAGATATTG | 23092 |
| rs386693045 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045723 | ATATGGCTGGTCAGG[CA/TG]CGGTGGCTCATGCCT | 23092 |
| rs386693046 | multinucleotide-polymorphism | GA/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055391 | CTAAAACTAGGAGTC[GA/TT]ATTAAGGGACCCAAT | 23092 |
| rs386693047 | multinucleotide-polymorphism | CT/GG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057152 | TCTTTCTAGCAGGCT[CT/GG]TTGTCATATGTGACT | 23092 |
| rs386693048 | multinucleotide-polymorphism | ACG/TCC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085012 | ATCGCGCCACTGCAC[ACG/TCC]AGCCTGGGCAACAGA | 23092 |
| rs386693049 | in-del | CTG/GT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095664 | ACCTCCACCTCCCAG[CTG/GT]GGTTCAAGCAGTTGT | 23092 |
| rs386693050 | multinucleotide-polymorphism | AAT/CCC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108537 | ACTTTGGTAGACTGG[AAT/CCC]TTGAAATAAAGCTAA | 23092 |
| rs386693051 | multinucleotide-polymorphism | AG/GT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114633 | ATTGACTGCAGCTTA[AG/GT]TACCCACCCACTTAC | 23092 |
| rs386693053 | multinucleotide-polymorphism | AGC/GGG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157367 | TGTTTTGGCAGAGAC[AGC/GGG]GTTTCACCATGTTGG | 23092 |
| rs386693054 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167396 | CTGAGACATGAGAAT[CA/TG]CTTGAACCCGGGGGG | 23092 |
| rs386693055 | multinucleotide-polymorphism | AAT/GAG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167416 | GAACCCGGGGGGGAA[AAT/GAG]GTTACAGTGAGCTGA | 23092 |
| rs386693056 | multinucleotide-polymorphism | AG/TC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188919 | GTTACACAGAAGAAG[AG/TC]AAGTCCCTGGGCTGT | 23092 |
| rs386693057 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195221 | CTTAATCATCCTGGA[CA/TG]TTGTCCTTGCAGAAG | 23092 |
| rs386693058 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220729 | TTAGTGATCTGAAAT[CA/TG]GCCAACTTTGGAGGC | 23092 |
| rs386693059 | in-del | AGA/C | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226788 | GAGTGCTTTTCGGTG[AGA/C]GGCAAAGAGAAAGAA | 23092 |
| rs397695776 | in-del | -/AAA | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904537 | AAGAAAAAAAAAAAA[-/AAA]GAGCCAAGAATACTC | 23092 |
| rs397705462 | in-del | -/T | 0.375 | 0.216506 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178017 | TTTTTTTTTTTTTTT[-/T]GAGACAGCATCTCAC | 23092 |
| rs397708556 | in-del | -/GT | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878557 | CATGTGTGTGTGTGT[-/GT]ATAAATGTGTAGTGT | 23092 |
| rs397714973 | in-del | -/T | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143058231 | TTCTATTCCTTAGTT[-/T]CCCCATCTGTCTAAT | 23092 |
| rs397715888 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812955 | TCTTTTTTTTTTTTT[-/T]GAGAAGGAGTCTCAC | 23092 |
| rs397720153 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791962 | AAAAAAAAAAAAAAA[-/A]GGTGTTAAGTTTTGA | 23092 |
| rs397725808 | in-del | -/C | 0.375 | 0.216506 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178890 | ATTTTTTTTTTTTTC[-/C]AAGGAGTCTCACTCT | 23092 |
| rs397729256 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022098 | TTCATTTATTTTTTT[-/T]GAGACCCCTGTCACC | 23092 |
| rs397735312 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076913 | TAGAGTTGTTTCTAA[-/A]GTTTTTAACATTATA | 23092 |
| rs397745314 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978765 | TTTTTTTTTTTTTTT[-/T]GTAAAAATTGAAAAT | 23092 |
| rs397749864 | in-del | -/C | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891613 | AGCTCTTAAGATGTC[-/C]AAGTAGCATATTGTA | 23092 |
| rs397751618 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905400 | ACAGCACTTTTTTTT[-/T]AATTTTAAATTTTTT | 23092 |
| rs397755690 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224119 | TACTTTTTTTTTTTT[-/T]GAAAAGATAAACTTG | 23092 |
| rs397757183 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781373 | GGTTAACTTTTTTTT[-/T]CTAAATATCTTCAAA | 23092 |
| rs397772851 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847374 | GTCTTTTTTTTTTTT[-/T]GAGACGGAGTTTTGC | 23092 |
| rs397781340 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788011 | TTTTTTTTTTTTTTT[-/T]AAGATGGAGTCTTAC | 23092 |
| rs397782242 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210898 | TCTGAAGGGCACTGT[-/T]GACAGGAGCAGCCGA | 23092 |
| rs397785687 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928252 | TTTTTTTTTTTAAAA[-/A]CTCATTGCCTTTTCC | 23092 |
| rs397788992 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992066 | TTAGGACTTTTTTTT[-/T]GTTTTTGAATATTCC | 23092 |
| rs397801587 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116003 | TAAAAATAGAATCGA[-/A]CAGGATAAGATGGGA | 23092 |
| rs397815910 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116025 | AGATGGGAATAGAAA[-/A]TATCAGAGTGTGTCA | 23092 |
| rs397817959 | in-del | -/CCTA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857644 | TAATTAATGACCCTA[-/CCTA]GCAAACAATGGCTTA | 23092 |
| rs397822080 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048936 | AAAAAAAAAAAAAAA[-/A]CCTTACCCAATCTAG | 23092 |
| rs397833830 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941099 | aatggaatatagatt[C/T]ttttttttttttttt | 23092 |
| rs397881562 | in-del | -/G | | | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768908 | TAGAGATGGGGGGGG[-/G]TCTCGCTGTGTTGCC | 23092 |
| rs397881686 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880530 | TCCAAAAAAAAAAAA[-/A]TCACTAGGAAACTCT | 23092 |
| rs397881708 | in-del | -/A | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964596 | ACAGCAGCAAAAAAA[-/A]CCGATGTTAAGAACT | 23092 |
| rs397882286 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786162 | ATTTTTTTTTTTTTT[-/T]GTAGCGATGGGGGTC | 23092 |
| rs397882460 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076180 | TTTTTTTTTTTTTTT[-/T]GAAAAGCCAGTCTCA | 23092 |
| rs397882481 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131874 | CAGGGGATGGCCAAA[-/A]TAAACAGTAGGGAGA | 23092 |
| rs397882484 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869392 | TATTTTATTTTTTTT[-/T]GTATTTTTAGTAGAG | 23092 |
| rs397882595 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837360 | TTCTGTTTTTTTTTT[-/T]CACCCTCTCCCTCTG | 23092 |
| rs397882821 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927346 | AAAAAAAAAAAAAAA[-/A]TCACTCTTCTGACTT | 23092 |
| rs397883394 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177988 | TCTGTGTGGCAGTCC[-/T]TTTTTTTTTTTTTTT | 23092 |
| rs397884101 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928265 | AAACTCATTGCCTTT[-/T]CCATCTCTTGAGTAT | 23092 |
| rs397884150 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928890 | CTGATATTTACTCCA[-/A]TTTCTCTTTCATTGT | 23092 |
| rs397884733 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855883 | TCTCCAGTGACTTAT[-/T]ACCAGGAATGTAGGT | 23092 |
| rs397885091 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035958 | AAAAAAAAAAAAAAA[-/A]GAAGAACTTACCCAT | 23092 |
| rs397946907 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088481 | TGTTAAAAAAAAAAA[-/A]GTGGTTATGTCTTTA | 23092 |
| rs397950704 | in-del | -/AATA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105423 | ATAAATAAATAAATA[-/AATA]TAAAAATAGGTCTAA | 23092 |
| rs397961384 | in-del | -/CT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898633 | TCTCTCTCTCTCTCT[-/CT]TTTGCCAAGAAGCTC | 23092 |
| rs397973559 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799201 | GTGGGTTTTTTTTTT[-/TT]GGAGGCATATTGTAA | 23092 |
| rs397976532 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204081 | TTAAAAAAAAAAAAA[-/A]TCACAGAAGTACTAT | 23092 |
| rs397999472 | in-del | -/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889964 | ATTTTTAATAGAGAT[-/G]GGGGTTTCTCCACGT | 23092 |
| rs397999474 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103581 | TGTATATGTGCCACA[-/T]TTTTTTTTTTATCCA | 23092 |
| rs398038872 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893953 | AACTCAACTCAACAG[-/A]AAAAAAAAAAAACCC | 23092 |
| rs398050800 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925098 | TTAAAACTGAAAAAA[-/A]TCTTTAACTGCTGAT | 23092 |
| rs398050801 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035958 | AAAAAAAAAAAAAAA[-/A]GAAGAACTTACCCAT | 23092 |
| rs398084521 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869391 | TTATTTTATTTTTTT[-/T]TGTATTTTTAGTAGA | 23092 |
| rs398084522 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880529 | GTCCAAAAAAAAAAA[-/A]ATCACTAGGAAACTC | 23092 |
| rs398084523 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931642 | TTTCTCCTCTTTTTT[-/T]TATCTTGAGTCCAGT | 23092 |
| rs398093787 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907953 | TTTATATAGTAGTTC[-/C]AGGAAGCCTAAGAGG | 23092 |
| rs398109488 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185353 | TGCCTGTTGTTTTTT[-/T]AACAATAAGTATGAA | 23092 |
| rs527249836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783155 | TGTGCTCTCCAGCCT[C/T]GTGGGCACATCTCAG | 23092 |
| rs527255589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107299 | TATAGGCCACGATGA[C/G]GTGTTTAGATTTGCT | 23092 |
| rs527262354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774979 | AGTTTATCCTTTCAT[C/T]TATTGAAGGACATTT | 23092 |
| rs527270838 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034210 | TCAAAAAGTTAAGCA[C/T]GGTGTCATTCTGTGA | 23092 |
| rs527283959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926564 | TTATTAGTTATCAGA[C/T]GTTAATTTTAAAAGG | 23092 |
| rs527292746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918695 | CTGAACTACTGAGGA[C/T]CCTAGGATTACATGG | 23092 |
| rs527299815 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032210 | TATTTGGTGCAAGCT[C/T]TGCCAGCATTCATGA | 23092 |
| rs527305070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185068 | AATACTGATGGTTGG[A/G]TAGTTTTCACACAGC | 23092 |
| rs527305952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193289 | GTCTCGCTCTGTCAC[C/T]CAGGCTGGAGTGCAG | 23092 |
| rs527309249 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830039 | TGGTGTGAGGAAATA[C/T]TGGCCCAGGGTGAAC | 23092 |
| rs527319804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147056 | GAGTCACCTGTTCCC[C/G]CTTGACTCTTCCTTT | 23092 |
| rs527325382 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179112 | TGACCTTAGCGATCC[A/C]CCTGCCTCAGCCTCC | 23092 |
| rs527328166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969763 | TGCACATGGGTGGTC[A/G]GTGTATCACGGCCCC | 23092 |
| rs527347039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072657 | AAACAAAGTTAAATA[C/G]TGCATATTCTCACTC | 23092 |
| rs527352955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065113 | TTCTTACTTGGTGCC[A/G]CCTTTAATTTTGGGA | 23092 |
| rs527366773 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976735 | GACATCTGGTTCCCT[C/G]TAGGTGGAATTTCAA | 23092 |
| rs527379069 | in-del | -/ACACACACAACACA | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222286 | CACACACACACACCC[-/ACACACACAACACA]CACACACACATCTGC | 23092 |
| rs527381702 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229254 | GAAGAGTCATAGTCC[A/G]CTTCACATTTCTAAC | 23092 |
| rs527384095 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877125 | CAATGACTGGATTAT[A/G]CTTTTCAGCTTGCCT | 23092 |
| rs527387947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057195 | GACATTTCCTTTGAT[A/G]TCTTTGATGCTGTCT | 23092 |
| rs527391017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065657 | GGCTTCTCCTGTTTG[G/T]ATTGCAGCCACCACT | 23092 |
| rs527397565 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214621 | ACACATTCCAGGCCA[C/G]AGCAGAGATGAGTTC | 23092 |
| rs527410971 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021368 | TTTGTTGAATCATTT[A/G]TCATTGTTAGACTAA | 23092 |
| rs527429499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015330 | GGAATATGTAAGGCT[A/G]TATGGTAGCTCATAG | 23092 |
| rs527430050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198779 | CTAAGTTTAAAGTTT[A/G]TTTAAAACTTCAGAA | 23092 |
| rs527440048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036796 | AGCACTTACCCAACA[C/T]TTATAGACCACTTAA | 23092 |
| rs527444805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114011 | GAGCCAATTACTTAC[C/G]TTCTCAGTGCTTCTC | 23092 |
| rs527445351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044317 | CTTCTTCTGGCTTCT[C/T]ATGTTCTCTGACCTC | 23092 |
| rs527446081 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962937 | AGTTATTTTTTTCCA[A/G]TCTTCTCCCTTCTCC | 23092 |
| rs527454495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990578 | TCTGCTCTGGTTTCT[C/T]CCCATCTTTGTGGTT | 23092 |
| rs527456193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906678 | TCTTTGTGTTGTTCA[A/G]TTACTGGAATTTTTT | 23092 |
| rs527459078 | snp | A/G | 3.30131e-05 | 0.00406269 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143134001 | ATATGCCTCTCACCA[A/G]TGCCCAGCTGCACCT | 23092 |
| rs527460433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087804 | ACAGGCATGTGCCAC[A/C]ACGCCTGGCTAATTT | 23092 |
| rs527461026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094796 | GTGGTTTGGGGGGAA[A/G]ATGGCTATGACAGAG | 23092 |
| rs527464945 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105857 | TTCTTGAAGCCACTC[A/G]CTGTTTGTTTTTAAG | 23092 |
| rs527465065 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841863 | TGTTTTCAGAGGGAG[G/T]TCCTGTTGCAGAATT | 23092 |
| rs527472567 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949394 | AGTAAGCCTTCATTT[G/T]TGCCACCGTCATCTC | 23092 |
| rs527488919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003572 | GATTGGAAATGATAA[G/T]AATGAAAAATTTTAT | 23092 |
| rs527491279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995430 | TCATCATCACTGGTC[A/G]TTAGAGAAATGCAAA | 23092 |
| rs527494114 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179847 | TCAGCCTGCATTTTG[A/T]CCCCACTCAACCCAC | 23092 |
| rs527506376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906180 | GGACACATGTGGTGT[C/T]GACCTGCCCCTCAGT | 23092 |
| rs527508878 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801341 | TAGAAATTGATGACG[C/T]CCTATGTGCCAGACC | 23092 |
| rs527509414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956562 | AGCCTGGGTGACAGA[C/G]AGCCTGTCTCAAACA | 23092 |
| rs527511854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218019 | CAGGCCTTCTTTATG[C/T]TCTCAAGTAAGGTCA | 23092 |
| rs527522877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948343 | TGTGTATATATGAAT[A/T]TGTGTGCATATGTGA | 23092 |
| rs527526733 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768703 | TAAAGCATTAAACAG[A/G]TTTACTTTCATAGGG | 23092 |
| rs527532483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858213 | TGATGTTAATTGGCA[C/T]GGTTTGTCACTAGTT | 23092 |
| rs527552484 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087695 | TTGTTGCCCAGGCTG[C/G]AGTGCAATGGTGCGA | 23092 |
| rs527560996 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817052 | GAGGGGACAGAGAGG[G/T]TGATGGGATTTTGCA | 23092 |
| rs527570482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140710 | TGAGTGCAAAAACAT[A/C]AGCAGCCTAGGACAC | 23092 |
| rs527577768 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050775 | ATGACAGGACCAGAA[C/G]ATGATAGACTACTTG | 23092 |
| rs527580457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141322 | AAAGCAGATACCATT[A/C]AGTATGATGTGAGTC | 23092 |
| rs527580603 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823415 | TTTTTTCTTTCTCTT[C/T]TTCCCTGCAGAAATA | 23092 |
| rs527590175 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148883 | GTTGAATTTCTAGCC[A/C]AAGTTGCTTAACATC | 23092 |
| rs527592119 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855937 | GAATAACAATAAATG[A/G]GTGGTCTTTATGGCA | 23092 |
| rs527604995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043628 | TAATATAAGGAAGAA[G/T]TAAGAGTCTAATAGG | 23092 |
| rs527620201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179445 | GTTGCTTTTTGTGAC[C/T]GACTTTCTGCTCTGC | 23092 |
| rs527624842 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823661 | AGGACCAAGGGTCTG[C/G]TTTGAAAAGTATTTT | 23092 |
| rs527625618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185728 | CCTCTTGATGTATGT[C/T]AACTCCTGCAGTCCA | 23092 |
| rs527628026 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011572 | GAGGTCTTCAAACTT[C/T]TCAAAGCCGCTATGC | 23092 |
| rs527633567 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002709 | CCTGAAACACTTTTC[C/T]GACTTGTACATTACT | 23092 |
| rs527648335 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993910 | TCCTGGGCGCATGTG[A/T]TCCTCCCACCTCACT | 23092 |
| rs527648728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131920 | TGCAGTCCTTGAGCT[G/T]TTCTTTCTATTATAG | 23092 |
| rs527650777 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142936 | GTTTGCCTTCCTATT[G/T]TTTTTAATATAAATC | 23092 |
| rs527651504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139636 | TAGCACCAACTACAC[A/G]GAGAGCGATATGTGT | 23092 |
| rs527652130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815602 | TCCCTGCCACCTTCT[A/G]GCACCTTCCCCTGCT | 23092 |
| rs527658806 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036473 | GGCCCCACTGCCTTC[A/T]TGCTGCTTCCTTTGG | 23092 |
| rs527661262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856842 | GCATCCATGGATTTT[A/G]TTATCTGTGGGGAGT | 23092 |
| rs527668029 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141968 | TCAGTTTTATTGGCA[-/T]TTTTTTCCCTTTGCA | 23092 |
| rs527680439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946300 | AGTTGTTGGTTTAAA[A/G]ACATTTGAGGCCATA | 23092 |
| rs527695605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000913 | GGAGAGCATTAGGAC[A/G]AATACCTAATGCATG | 23092 |
| rs527710170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216340 | ACAGAGCAGCGAGAG[G/T]GATCTTTGAAAAACG | 23092 |
| rs527715659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954205 | TTCTTTCCATGAAAT[A/C]TAAGAATGTTAGGCC | 23092 |
| rs527720367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863196 | GCTCACTGCAAGCCC[C/T]GCCTCCTGGGTTCAA | 23092 |
| rs527730597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869799 | ATTTGGGTTAAATTC[A/T]CTTAAATCCGGTGCA | 23092 |
| rs527752596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953715 | GTGAGGTAAAACTTA[G/T]GGAGTGCCAACTGAC | 23092 |
| rs527754240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961319 | AACGTGGTGAAACCC[C/T]ATCTCTACAAAAAAT | 23092 |
| rs527759753 | in-del | -/TC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093591 | CTCTGCCTCACTCTT[-/TC]TCTCTGTCTTTGACT | 23092 |
| rs527765864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822167 | TGCCTTTTGCCTAGA[A/G]TTGACTCACTCTCCA | 23092 |
| rs527768549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056294 | CATTGAATTTACAGC[A/G]GAGGACAGAAACTTC | 23092 |
| rs527773937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048685 | CTTTGGGAGGCCGAG[A/G]AGGGCGGATCACAAG | 23092 |
| rs527775912 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169597 | TCTGTTGGTCCACAT[C/T]GAGTCCCATCCCCAT | 23092 |
| rs527789199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968076 | CCTCCTCTTCCTCTT[C/T]CTCCTCCTCCTATTC | 23092 |
| rs527793302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869317 | GTTCACGCGATTCTC[C/T]TGCCTCAGCCTCCCT | 23092 |
| rs527794375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960836 | CAAGCTATTTCCCAC[A/C]TTGGGACTTTTGCTC | 23092 |
| rs527796987 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118948 | AGTATAATAATAAAA[A/G]AAAAAAAAGAAAGAA | 23092 |
| rs527798801 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776554 | TGTTTGAGGCTCATC[A/G]TGTTGTAGCATGTAT | 23092 |
| rs527820038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098729 | TTCAATTCCTCCGAG[C/T]CTCAGTTTTTTCATC | 23092 |
| rs527843710 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890332 | CAGAATGAACACCAG[A/G]TGAAAAGGTTGTGGG | 23092 |
| rs527849141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211174 | GAAGATAAGACTTTT[G/T]GGGTAGGGTTGCCAG | 23092 |
| rs527853044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029655 | TTCAGGCGATCTTCT[C/T]GCCTCATCCTCCCAA | 23092 |
| rs527853811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119712 | TAACTGGGCTGTGCC[A/G]CAGTTAAAGTTTCAT | 23092 |
| rs527854056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205173 | CTTAGCCCTCAACTG[A/G]TGGATCTTACTGTCT | 23092 |
| rs527859844 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015428 | AGAAAGGGTCTTCTG[A/G]ATAATACGACAAAGC | 23092 |
| rs527861225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932480 | GAGCCTGGTAATATG[A/G]TCCCTGCTGCCATTT | 23092 |
| rs527886131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844479 | AGTTCAGGACAATTT[A/C]CCAAGAAAAAGCCTC | 23092 |
| rs527897790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851386 | ACAGGCGTGAGCCGC[A/T]GCGCCCAGCCGGAAA | 23092 |
| rs527900096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843936 | TGGTGTGCTCCTGAG[C/G]CTTGGTTTCCTCATC | 23092 |
| rs527900655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795807 | CTGAATTTATCCCCA[A/G]AATCTCAGCCCTATT | 23092 |
| rs527903671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931931 | TGTTTTGCCCCTCTT[C/T]GTGTTGTTAACCTTA | 23092 |
| rs527904194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939436 | GATATCTTCTGTTTT[C/T]GTCTTTGTGGACTTT | 23092 |
| rs527916589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071726 | CAGTCTGGCCAACAT[A/G]GTGAAACCCCATCTC | 23092 |
| rs527924768 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829957 | CAGGCCTTTATACCA[G/T]TATTACTTTGGGGAG | 23092 |
| rs527928756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165013 | CTTTACTTCGGATTC[A/G]TATAGAAATCCAAGA | 23092 |
| rs527934147 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810447 | CTTCATAATATTTTA[A/G]TGAACATGCCTTTTT | 23092 |
| rs527935961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086812 | CTACAGAACTAACTT[C/T]AGTTGATATGGAGGG | 23092 |
| rs527939031 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036732 | ATATGGGCTAGTGAT[A/G]ATGTCAACCTGGAGG | 23092 |
| rs527939275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079714 | ATGTGTACATTGGAC[C/G]TATTTTACCTGTGGA | 23092 |
| rs527951986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850929 | TAGCATTAGAGTGGT[C/G]GATAAGCTCGATATG | 23092 |
| rs527954042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132459 | GAATAAGAGATGGTA[A/G]TGAGTGGATCCATAA | 23092 |
| rs527954350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889863 | TACAAGGCCTGGCGC[A/G]GTGGCTCATGCCTGG | 23092 |
| rs527954618 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125703 | TAAAATTAATGAATC[A/C]TTTAAATGAATACAG | 23092 |
| rs527954855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171820 | TTTGCAAGCCCAGTA[C/T]TTATCTCTGGCGTAG | 23092 |
| rs527970897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216587 | ACATACAACATGGTC[A/G]TCATCATAAATCCTA | 23092 |
| rs527974612 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989966 | GCAGTATCTTTGTGG[A/C]TTTCTCTGTATTTCC | 23092 |
| rs527981830 | in-del | -/AAG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204863 | GTAACCACTGACCAA[-/AAG]AACAGATTGGTACAA | 23092 |
| rs528010023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994470 | ACCATAAAGGATTTG[A/G]GCAGAAGTGATTTCA | 23092 |
| rs528015674 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126558 | TTAACCATACTGTTC[C/T]AAACTTGCAGCTCAG | 23092 |
| rs528019841 | in-del | -/AGA | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:142919907 | TCAGGAGGCTGAGGC[-/AGA]AGAATTTGCTTGAAC | 23092 |
| rs528021694 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055340 | ATTGGCTATTGGGTA[A/G]TTAGAGTCAAGAGTA | 23092 |
| rs528031300 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788069 | CATGTGGCATGATCT[C/T]GGCTCACTGCAACCT | 23092 |
| rs528043591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806373 | GTGCTGGGATTACAG[A/G]CCTGAGCCATTGTGC | 23092 |
| rs528052720 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941251 | ATTGTGTTCTCTTTT[C/T]TCCACAACCTCACTA | 23092 |
| rs528062007 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927948 | TAGCCTTATTGGCCA[G/T]TTGGATGTCCTCTTT | 23092 |
| rs528062723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174802 | GTAATTGGAACCCTC[A/T]GCCAAATACTTGCTG | 23092 |
| rs528067515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854147 | CACTTTGATAAACTC[A/T]GTTACCTGTATACAT | 23092 |
| rs528073283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089855 | CATAAGGGCCTTCTC[C/T]CGCTTCACGATGTCT | 23092 |
| rs528078250 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857027 | AATCATTCCTGGCCT[C/T]TTCCTGGCTTTCCTT | 23092 |
| rs528080790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943432 | TTTTCTGATTCATAG[A/T]TGGCACCTTTTATCT | 23092 |
| rs528081682 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994791 | ATAGTGCCAGCTGCT[C/G]TGCTGCTGCTACCTT | 23092 |
| rs528100740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175834 | ATATGGCACAATAGG[C/T]CAGGCACAGTGGCTC | 23092 |
| rs528106890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083704 | GGGTTTCACCATGTT[C/G]CCCAGGCTGGTCTCA | 23092 |
| rs528115545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951209 | AGATTACAGGCATGT[A/G]CCACCACGCCCAGCA | 23092 |
| rs528116641 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860149 | ACATGCTCCACTGTC[A/G]CACTGGATCTCACTT | 23092 |
| rs528121787 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809790 | CATTCATTCATCCAC[G/T]TAGTGGCTCACTTCA | 23092 |
| rs528130660 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866943 | ATACCCCTCCCACTC[A/C]ATGTCTCAGGCTTGA | 23092 |
| rs528134950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096503 | CGTTTACATGGTGTT[G/T]CATGAAAAAAGAGGT | 23092 |
| rs528138493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893880 | TTGGCTATTTGTGTG[C/T]CTTCTTTTGAGAAAT | 23092 |
| rs528139541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950643 | AGTTATTGACCCAGA[A/G]AGTCAACCTCAAGGT | 23092 |
| rs528144416 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163639 | TATTTTCAGTAGAGA[C/T]GGGGTTTCACCATGT | 23092 |
| rs528170216 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226671 | TGTCCTAGAATTGGA[A/G]CCAGTCTTTAGCTTA | 23092 |
| rs528171852 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142770208 | GCTGCGGACCTAGGC[C/G]TTGGCGAGGGCCACG | 23092 |
| rs528174376 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832586 | AACACTTATTTCAGG[A/C/T]CTTTTGTGTGCCTGG | 23092 |
| rs528178799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812487 | GGATTACAGGTGTGC[A/G]CCACCATGCCCGGCT | 23092 |
| rs528181710 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136243 | GTCCAAGATTAATTT[A/T]ATCACACAAGGCAGA | 23092 |
| rs528182803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908014 | CTTAGCTCTAACTTA[C/T]GTTAGGAACTGCAGT | 23092 |
| rs528184726 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807453 | CAGCGCTTCAGTTCA[A/G]CTGTGCTGCTGAGGT | 23092 |
| rs528188704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219930 | TCCAACCCAAAGGCT[A/G]TGTTATCTCCTGCCA | 23092 |
| rs528188764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142694 | AAATTGCTTCAGAAA[A/G]TCTGATTCCAAGCTT | 23092 |
| rs528200259 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181313 | CAGCGTCTGTTTACA[C/G]TCTTTACTTTGACCT | 23092 |
| rs528214699 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996977 | ATTAGTACAACCATT[A/C]AAAACCTAGTAAAGT | 23092 |
| rs528215879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045796 | TGAGGTCAGGAGGTC[A/G]AGAGCAGCCAGGCCA | 23092 |
| rs528222030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907505 | CCCTGGGGGAAATCC[C/T]GGGGTTGGTTTCATT | 23092 |
| rs528235561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887632 | CTTTCTAAGTACTTT[C/G]AGTGTAAGGATTGGG | 23092 |
| rs528241991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202111 | TCCTGTATTAGGTAC[A/G]TATATATTTAGGATA | 23092 |
| rs528243793 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116527 | ACTGCTTAGCACTTA[C/T]AGAGCTCTGGCTCTC | 23092 |
| rs528250628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980260 | TGTAGAAAGCATTTC[A/G]TTGTACAGAACATAT | 23092 |
| rs528259650 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076400 | TGTGCACAGTCTCCC[C/T]CTTCTCCCTTTTTTT | 23092 |
| rs528265440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929727 | CGAACTTCCTCTGTG[A/G]CTTGGGGTGGAAATC | 23092 |
| rs528272103 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161831 | TTACCAAAGCAGTGA[C/G]ATAGAAATCATTCTG | 23092 |
| rs528277689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040653 | GGAATGACCAGTAAT[A/G]TTGATTGTGGATTGC | 23092 |
| rs528281391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117181 | TGACATTCTGAGCCA[C/T]GTGAGGAGGAACTCA | 23092 |
| rs528282051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077111 | GATCGATGGCTAGAT[A/G]TGGATACAGAATACT | 23092 |
| rs528290489 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833061 | AACTTTTATTTCTTT[G/T]TTTTTGTTTTTGAGG | 23092 |
| rs528303145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840625 | GGGCCCATGGCAAGT[A/G]GTAGTTGTCATCGTC | 23092 |
| rs528304163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880338 | GGCTGGCCAATATGG[C/T]GAAACCCCGTCTCTA | 23092 |
| rs528313162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936563 | CAGAAACCAAAATAG[A/G]TAAAACAATTTTAAA | 23092 |
| rs528315531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155468 | TGGAAATTCCTGCCT[G/T]CATCCAATTTTTATG | 23092 |
| rs528333344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162228 | CATGGTAGGAGCTCC[A/G]TATAACTCTGCTTCT | 23092 |
| rs528342939 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102079 | CAAAACTATGTGGTA[A/G]GTGGAACTGGGTAGG | 23092 |
| rs528343183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084208 | AACTGTGGTCACAGT[A/G]TTCCCTGCCATTAAA | 23092 |
| rs528348875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122555 | ATTGACTTTTATTTG[C/T]GATTCTAGAATTGGG | 23092 |
| rs528361338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214345 | GTTACCACTGTAAAT[A/G]AGATTGTGCCTGCAA | 23092 |
| rs528363980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129449 | ACAGCGCTAGTAAGT[A/G]ACTAAAATCAGATCC | 23092 |
| rs528364672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979633 | AAATTTCTTCCATAC[A/G]CAATCAAGGAAAAAG | 23092 |
| rs528367285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987208 | CTTGAAGAGGTCCTT[C/T]ACGTCCCTTGTAAGT | 23092 |
| rs528367433 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887095 | CTGGGAGGCCCACAG[A/C]ACAGTTACCCTGTAG | 23092 |
| rs528373220 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791584 | TAAATTGACAAAGCC[A/G]TTTGTTTGTGTATAT | 23092 |
| rs528374853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032578 | CTGTCGTTAGCAAAC[A/G]CAGCTTGGTGGTGAT | 23092 |
| rs528375361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208211 | GAGCTCTTTACAACC[A/G]GGAAAAGAACGAATA | 23092 |
| rs528381924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800519 | AGGCACCTGCCACCA[C/T]GCTCAGCTAATTTTT | 23092 |
| rs528384812 | in-del | -/TG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917500 | AAACTACAATGAAAC[-/TG]TACAATATAAAGTAC | 23092 |
| rs528388582 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807516 | CTGCAGGCCATGCTT[A/G]GCAAAACCTCCCTGA | 23092 |
| rs528397839 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986718 | AGTTTCAGCTTTCTA[C/T]ATATGGCTAGCCAGT | 23092 |
| rs528398310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893868 | TTAATATACCCTTTG[C/G]CTATTTGTGTGTCTT | 23092 |
| rs528401043 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944248 | AGCATTTTTGACATA[A/G]TAATAGCTTTAGTAA | 23092 |
| rs528401161 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010365 | AGGTTCCATATCTCT[A/G]AAATGTGAATAATAC | 23092 |
| rs528409830 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784324 | ATAACTTTGGCTTGC[C/T]TCTCATCTCCCCCAC | 23092 |
| rs528410814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025124 | CCAAAGCCAGAGCCC[A/G]TTTATATAAAAACGT | 23092 |
| rs528414263 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950465 | AGAGAAGTAGTATCA[A/G]TGCTGCATGTTCTTT | 23092 |
| rs528419211 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033042 | TCTGTTTATAGGCTG[G/T]AAATAATTATCATCA | 23092 |
| rs528422542 | snp | A/G | | | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216794 | AGAAAACACCTCTCA[A/G]TGTTGACTGAGTTGC | 23092 |
| rs528425784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123268 | CCTTCATATTCATAG[A/G]GTTTGTCGTCTTTGT | 23092 |
| rs528447096 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985862 | TATGGCTGCATAGTA[A/T]TCCATGGTGTATATG | 23092 |
| rs528447449 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023590 | ACAGTTGAGAGGCAG[C/G]AGGAGGCAGCCACCG | 23092 |
| rs528447906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934669 | AGTCGGTGTTAGTGT[C/T]GTTGCCTTATTTCAG | 23092 |
| rs528451350 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927541 | TGTATGGTATGCCAT[C/T]GTTCAAATATACAAC | 23092 |
| rs528460753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885057 | GGGAATCTTGGCTTT[A/G]CCACCATTAGATATT | 23092 |
| rs528462402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159598 | TTACCAACATCTAGG[C/T]CCCTTCCCTGGAGCC | 23092 |
| rs528468781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114740 | GGTCATGATCCAGCC[C/T]CTAGTCCTAAGGTAT | 23092 |
| rs528480596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082685 | TCACTATACTGTAGC[C/T]GCACATAAGCGTAAT | 23092 |
| rs528484368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934096 | CCCAAACCCACTACT[A/G]TCTCTCCCCCTGCCT | 23092 |
| rs528488810 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006975 | TGGCTCATGCCTGTA[A/G]TCCTAGCACTTTGGG | 23092 |
| rs528492989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024146 | GGGCTGGAGAGAGAA[A/G]AAGGGGCAGGAACAG | 23092 |
| rs528495405 | snp | C/T | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965825 | TCAGTAGGATGCTGC[C/T]GAGACCTAGCCACAG | 23092 |
| rs528505460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798531 | TATTGTGCTCTGACT[A/G]TGCTCTCAAATGGAG | 23092 |
| rs528506401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115190 | ATACAAAAGTTAGCC[A/G]GGCATGGTGGTATGC | 23092 |
| rs528513435 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839983 | ATGTTCTTTTGGTTG[A/G]GGCAGTTGCAGTGGT | 23092 |
| rs528517363 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160320 | TGCCTCAGCCTCCCA[A/C]AGTGCTGGGATTACA | 23092 |
| rs528533915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797711 | TAAGGCAGGTATTTC[A/G]GTTTTGCAGCTTCAT | 23092 |
| rs528538316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845562 | TACTGTCTTTGTTAT[A/G]TGCTCTAGGTGGCCT | 23092 |
| rs528549492 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048920 | CCATCTCAAAAAAGA[-/A]AAAAAAAAAAAAAAA | 23092 |
| rs528553128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781215 | TGTGGTCACTAATGA[A/T]CAGTCATGTGAAGGG | 23092 |
| rs528556393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127708 | CTTGATCTGCTTTTA[C/T]CAAAATATTGGTGAC | 23092 |
| rs528575528 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867486 | GTTGGAAATGCCTCT[A/C/T]TCCAAGCACAGTTTC | 23092 |
| rs528579251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805153 | TTTTCGCCAGGCTGG[A/C]GTGCAGTGGCGCAAT | 23092 |
| rs528586428 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227635 | TACAGTACCTGTCTA[A/T]CTAAAGAGCTTCCCA | 23092 |
| rs528587953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212735 | GACCATGTGGCTCAC[A/G]AAGCCTGAAATATTT | 23092 |
| rs528588126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218859 | GGTGACAGACTCTGG[A/G]ATCAGATGTCTTGGT | 23092 |
| rs528591814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206443 | CAAACTTTTGATTAG[C/T]TACCCGTCAAGGAAC | 23092 |
| rs528602873 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213101 | AGTGAGCCGAGATCG[C/T]ACCACTGCACTCCAG | 23092 |
| rs528610843 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892778 | TCAAATCAAGGTATT[C/T]AGGGTATCAGTCACC | 23092 |
| rs528620657 | in-del | -/CTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201774 | TGTCTGTTTACAGTC[-/CTT]CTGTTGCGACATGCA | 23092 |
| rs528625102 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128266 | AATATTACTCAAATA[A/C]AGGTGGAGATTGTTG | 23092 |
| rs528629995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990959 | CAGATCTCAAACTCC[A/G]TGTTGGGAGAACCAC | 23092 |
| rs528636002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142891214 | AGCAGCCACACGATG[C/G]AGGGGGTGGTGGTGG | 23092 |
| rs528636192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121364 | CAACAGCCATGGTTA[C/T]GGTGGTGGCAGTGGT | 23092 |
| rs528640372 | snp | G/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864792 | CTGTGAGGTACATAC[G/T]GTCCTCACAGTTACA | 23092 |
| rs528645337 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951162 | CCTCCCAGGTTCAAG[C/G]GATTCTCCTGCTTCA | 23092 |
| rs528654198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777558 | TAAGTTTCTGAGTGA[A/G]CCTCGTTTTACCTTT | 23092 |
| rs528659429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004399 | TCCAAATCCATTTCT[C/G]CCTGTTTTGGAATCT | 23092 |
| rs528660405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914162 | CACCTTTCCCTGGCT[C/G]TATGGCATCCTGAGA | 23092 |
| rs528676244 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187563 | TTTTCTGAGCCATCC[A/G]CCCTGTGGAAGCCAC | 23092 |
| rs528677494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011597 | CTATGCCCTTCCTCA[A/G]TAGCCACATGAGTAA | 23092 |
| rs528686319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776886 | CATTCCCACCAACAA[C/T]GTATGAGGATTCTGA | 23092 |
| rs528687379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921383 | ATTTTATTTTTTATG[A/G]TGACGTAATTTTGAC | 23092 |
| rs528702056 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977853 | TCAGCGAGCTCTGGT[A/G]TCTTGTGTTTCTCTG | 23092 |
| rs528705949 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784725 | AGCTTTTTTGAGATA[A/C]AATTCACACGACACA | 23092 |
| rs528708947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964902 | CACTACCACCAATGC[A/G]CGGAGACCAGTGGTG | 23092 |
| rs528709756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148878 | GCAAGGTTGAATTTC[C/T]AGCCCAAGTTGCTTA | 23092 |
| rs528713920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872364 | TCTTATTAAAGCCAG[A/G]CCTTGTTGCTGGTTC | 23092 |
| rs528718677 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133802 | ATGTTTAATGCCATT[G/T]CCTAGAAAAGTTTAA | 23092 |
| rs528723160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052393 | GAGAATCGCTTGAAC[C/T]CAGGAGGTGGAGGTT | 23092 |
| rs528726535 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142217 | GATCTTGGCTCACTG[A/C/T]AACCTTCGCCTCCCG | 23092 |
| rs528730241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060383 | TGATTTCCCTTAGCC[A/G]CAGAGGGAGATTTAA | 23092 |
| rs528771044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879313 | CATGCTGGAGCTGCT[A/G]TAATTCTTTACTGAT | 23092 |
| rs528771127 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160964 | CTCGCTCAGGAAGCT[C/G]AGTAGAACCAGTTAG | 23092 |
| rs528784133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878782 | GTGCGTTTGAGGTGC[A/G]TTGGAGTGCCAGTAG | 23092 |
| rs528784621 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970800 | TACTAATAGAAGTTT[A/C]TGTAAGATGTGGGTG | 23092 |
| rs528790458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059558 | CTCCTCCTTTTCCCA[C/T]CCTTTCCCCCTCCAG | 23092 |
| rs528791749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791695 | TTGGCTGGGCATGGT[A/G]GCTCATACCTGTAAT | 23092 |
| rs528795316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154470 | GTATTATTTTGGAGG[A/G]CTCCCCCCACAAACT | 23092 |
| rs528797438 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156839 | TTTTCACAGGAACCT[A/G]TTAGCTCACCAGGGC | 23092 |
| rs528799126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193993 | AGATGAACAAGGGTC[A/C]GTTGTCCACACTGAC | 23092 |
| rs528805826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978503 | GTGGCCAAGAGGGTG[A/G]TCTGGTTTCAGACAA | 23092 |
| rs528808360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148310 | TTTTCCTGCTCCTCC[A/G]CATGCCATAGTTTCA | 23092 |
| rs528821179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920713 | AGGATATTTAGTGCT[A/G]GAGTTGTAATAAGGG | 23092 |
| rs528826551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790960 | TTGAATAAATGATGT[C/T]GAATGTTCCTTTAAA | 23092 |
| rs528833981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931765 | CAAGGAATTGAACAA[C/T]GTCTAAAGGCATCAC | 23092 |
| rs528834179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974487 | ATAGATGAATTCATA[C/T]ACAAATATTGCTTAA | 23092 |
| rs528837858 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134765 | ACAGTATTGTTTCAG[C/T]CTTTGCTCTAAGAGA | 23092 |
| rs528838994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017465 | AGATGAATTCATCAC[A/G]CTCCCCTGTTCATGG | 23092 |
| rs528844214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163583 | AGCCTCCCAAGTAGC[G/T]GGGATTACAGGGGTG | 23092 |
| rs528847268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982642 | ATTTTATCTGCCCAG[C/T]GACTGATCTTAGCCT | 23092 |
| rs528849529 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213758 | ACATGGCACAAGGTG[-/A]ACCCCACAAAAAGTG | 23092 |
| rs528852256 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835674 | ATTTTCTATGTTCAT[A/G]GAGTTCCCTGAGCTT | 23092 |
| rs528866231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111798 | TGGCTGTTATACCTT[C/G]CAGATTGTCCAGGGA | 23092 |
| rs528892531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021427 | ATAACATTGGCCTAT[A/G]TTATTCATAATAGCT | 23092 |
| rs528897008 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879158 | AAATAATCAGTATTA[A/G]TCATGCATGGGAGGA | 23092 |
| rs528899029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063281 | AGTACTCCTGTAGTC[C/G]AAGCTGCCATTGTGT | 23092 |
| rs528903557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157379 | GACAGCGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 23092 |
| rs528907355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938254 | TTATAACTTTAAAAA[A/G]CAACAAAGTTAGCTA | 23092 |
| rs528918257 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889690 | CTATTTAAAATAACA[A/T]AGTCAATGAAAGCCT | 23092 |
| rs528921759 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111818 | TTGTCCAGGGAGAGA[C/T]GCCTAGTGCATTATA | 23092 |
| rs528922568 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083827 | TTAACTCCGATTCAA[C/T]ATATCTTTCTCCCAT | 23092 |
| rs528925425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070954 | ACATTCTTCACAAAC[A/T]TAGAAATAAAAAGTC | 23092 |
| rs528930022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163172 | AGACTAAAATATACT[C/T]TCCTTGCTGCTGCTC | 23092 |
| rs528961726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124855 | GGTACCCAGCAAGTT[A/T]GCATTTAGTTCCCTT | 23092 |
| rs528962564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809066 | TTTATCAGAAATTTA[C/T]AGCTTGGTTTTCAAA | 23092 |
| rs528972679 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081095 | TGTTTTATTGTTGTG[A/G]TGGAGTGGGTGGGTG | 23092 |
| rs528973618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982104 | AGCCCTGTGACCAAA[C/T]GTTTAGCAGGCTGTT | 23092 |
| rs528975329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802715 | CTGTATTGAAATACA[A/G]TGCACATACTAGGGC | 23092 |
| rs528981563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203674 | CTTGGAACCAACCCA[A/G]ATGCCCATCAGTGAT | 23092 |
| rs528987158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079574 | CCAGCCTGGTATTGT[C/T]GGCCCCATACAAACC | 23092 |
| rs528989586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989105 | GTGTTAAATTCTCCC[A/G]TTATTATTGTGTGGG | 23092 |
| rs528990918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070430 | ATAGGCACATACCTA[C/T]GCATAAATTTAACTA | 23092 |
| rs528990945 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802015 | AGAACATCAGAGGGG[A/T]TCTGTTCCCTCTTAA | 23092 |
| rs528991387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896408 | GTAGGCGTACCTAGT[A/G]AGTCAGGTATTTTAT | 23092 |
| rs528995298 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136672 | AGCTAGGAGCTGGAA[C/G]GTTCTGCTGGGACCT | 23092 |
| rs528998041 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107023 | TCTTCATGGCACTTC[C/T]GTAATCTGACATTTT | 23092 |
| rs528999727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210160 | TGGGAAGAAAAAGAC[A/G]TTTAACGGACTTGCA | 23092 |
| rs529019586 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125450 | CACAACTTGTGTTTG[G/T]TCAGATAGAGTGCAC | 23092 |
| rs529021862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027531 | TTATTAATTTGCTTA[C/G]TGGTTTTAAACCAAT | 23092 |
| rs529049403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918447 | CCACCGTGCCCGGCC[A/G]AGGATCCTTTTTAAA | 23092 |
| rs529066293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911474 | TTTCCTAACCTTCCT[A/G]ACCAGGTCAGATCTC | 23092 |
| rs529068710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184301 | AAATATTCAGGCCTC[C/T]CCCTAACCTGAATTA | 23092 |
| rs529071997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829006 | ACTACTGGTGTGTTA[C/T]TGGAAGTTAGCCACT | 23092 |
| rs529083607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917916 | GATATCCTAGCAGTA[G/T]TATCACTTGTCAGCT | 23092 |
| rs529090615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961383 | TGCAGTTCCAGCTAC[A/G]TGGGAAGCTGAGGTG | 23092 |
| rs529101190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099492 | AAGGATGGACGAGAT[A/T]AAAAATCTACTTTCT | 23092 |
| rs529104809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146277 | CATTTATGATTCCAA[A/G]TTTTTAAAGATGGGA | 23092 |
| rs529117280 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008549 | AGAAAACCTCAGGGG[A/T]TCATAGAGTTTGGAT | 23092 |
| rs529126568 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882407 | GATACACACAGTTCA[C/T]TTGTTTAAAAAATAT | 23092 |
| rs529131877 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064183 | TCCCCCAGGGTGTGC[A/C]TTCTCCAGTTTGCCT | 23092 |
| rs529134508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139023 | TTGTGACCTAGTCCG[C/T]GAACTCTTCCTTATC | 23092 |
| rs529135341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968984 | TCACCCAGACTGGAG[C/T]GCAGTGGCGCACTCA | 23092 |
| rs529139834 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924745 | ACGCATAGTAGTGCA[A/G]ATTCATATGTTCTGT | 23092 |
| rs529146216 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151568 | CAAACTATGGTGCAC[G/T]CAGACAATGCTATAT | 23092 |
| rs529149435 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874296 | GCACACTATTCTTCT[A/G]TAGGCACCTTGGTTG | 23092 |
| rs529151400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968162 | CCTCATAACAACTCT[A/G]TGAGGTAGGTCGTAT | 23092 |
| rs529163954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967564 | AGGCAGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 23092 |
| rs529168383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197609 | TAGTCTGGTTATAAA[A/C]CCTTTGTTCATTTTT | 23092 |
| rs529181844 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225136 | ACTATTACGCTTCTC[A/G]AAGAGAGACCAACAT | 23092 |
| rs529186355 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772191 | TTGCTTCTAAAAATG[-/AA]GAGAGAGACAATGGA | 23092 |
| rs529189105 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152121 | GGGTATTTTTTTCGC[A/G]GTGAGACTATTCTGT | 23092 |
| rs529192776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780814 | CTGGTCTAGGGGACA[C/T]GTTGCCTATCATAGA | 23092 |
| rs529193379 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161334 | TCCTATTAAAATTAG[G/T]GAGCCCTAACTTAAG | 23092 |
| rs529193461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190981 | GAAATATCTAGAAAA[A/G]GCAGATCTCTAGAGT | 23092 |
| rs529203467 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221943 | GGAAGGAAGGAAGGA[A/T]GGAAGGATGGAAGGA | 23092 |
| rs529207979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875473 | ACTTTTTTGGGCGTC[A/G]GATTCTCTACCAGCA | 23092 |
| rs529209716 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145787 | TCACAGGGTTTTTCT[C/G]TCTCCTGTGGGGCTT | 23092 |
| rs529214836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895460 | TGGTCTCGATCTCCT[C/G]ACCCCGTGATCCGCC | 23092 |
| rs529217062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925084 | TTTGAGGCAACAGTT[G/T]AAAACTGAAAAAAAT | 23092 |
| rs529218090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795612 | ATGTACTTGTTTTGC[G/T]TCCAGCCCCAAATTC | 23092 |
| rs529228352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917100 | GCCGGAGTGCAGTGG[A/C]ACGATCTCAGCTCAC | 23092 |
| rs529232655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827460 | CCCTTTATTATTAAT[A/G]GTTGTAGAATTTGTG | 23092 |
| rs529232769 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105805 | TAGCTGCACCGGGGC[A/G]TTATGGGAAAGTAAC | 23092 |
| rs529235360 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788104 | CTTCCAGGTTGAAGT[A/G]ATTCTCGTGCCTCAG | 23092 |
| rs529240583 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929914 | AACTTTGCTCTCTAG[G/T]GCAGGGGGAACAGGA | 23092 |
| rs529251877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014544 | GGAGAGGCAATAACT[A/G]TGTTAGGTGATTTCT | 23092 |
| rs529252297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915588 | TGGTCCTGAACTCCT[G/T]ACCTCAAGTGATCCA | 23092 |
| rs529254055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188985 | ATGGAACAAGCGACA[G/T]ACTCTTTTAAGGGTG | 23092 |
| rs529258087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779050 | TGATATGCTTTCTGA[A/G]TGGCATGTTCTTATA | 23092 |
| rs529259305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142771991 | CCACATGAAGGCAGA[G/T]AGTGGAATTGTCTCT | 23092 |
| rs529274543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104000 | AAAGGAGATCCTGCT[A/G]TTTGTTACAACATGG | 23092 |
| rs529286312 | in-del | -/ATAAGTGA | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901317 | TTTAGGGAAACCACC[-/ATAAGTGA]AAATGTGGGAATATG | 23092 |
| rs529286665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005946 | TCGGCACCAACAGGT[A/G]CAGAACCCCTTTCTT | 23092 |
| rs529288200 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774525 | GTTGCCCCTATTTCT[A/C]ACATCCTGCATTAGC | 23092 |
| rs529311020 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114018 | TTACTTACCTTCTCA[G/T]TGCTTCTCTTTCCTC | 23092 |
| rs529312374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826548 | ACGGTGAGTGGACCA[A/G]GCTTGGGTTGTCCGT | 23092 |
| rs529321085 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839123 | TTCAGACGATTCTTA[A/T]GTATTTTATAAGTTT | 23092 |
| rs529321160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182319 | TCCACAGTTCATCAT[C/T]TGCTGAAGAGTGGCT | 23092 |
| rs529321161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189677 | CTGCCTTAGTAATTG[A/C]TATATTACACACATT | 23092 |
| rs529322949 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149485 | ACCCCAGGCAGTGAG[A/G]TGATTTTCCTGGGAT | 23092 |
| rs529329673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834504 | CCAAGCCTTTGAGAC[C/T]AAAGATGACAATAGT | 23092 |
| rs529333040 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054840 | ATAATCTGTTAAGAA[A/C]ACAAGGAATCATGAA | 23092 |
| rs529348960 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151007 | TAGGAGAAAATATTT[A/G]CAAAACACATATCTG | 23092 |
| rs529354662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966686 | GAAGAAAGATAAAGA[C/T]TCTATACAGGAAAAT | 23092 |
| rs529368623 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795083 | ATAGCCCTTTAATAA[-/T]GTAAAAACCATTCCT | 23092 |
| rs529374812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069523 | TCTCCTGGGTAAGGT[C/T]CCCACATCTGTACTA | 23092 |
| rs529378820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873789 | TGGTGACATTCTTCC[C/T]CTTCAACCATAGTAC | 23092 |
| rs529400040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793735 | TGGGATTACAGATGT[A/G]CGCCACCATGCCTAG | 23092 |
| rs529408260 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083608 | GGTTCAAGCGATGCT[A/C]CTGCCTCAGCCTTCC | 23092 |
| rs529418992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808381 | CCAATCATCTAATTG[C/G]TGTCAAATTTTGTTT | 23092 |
| rs529421564 | in-del | -/CTGA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906953 | GAAGTCCTTTGCAGG[-/CTGA]CTAATGCCTTCTTCC | 23092 |
| rs529426328 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923008 | TAGTTTCTGAATTGC[G/T]TTTTGGCTGTTCTGT | 23092 |
| rs529428274 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817433 | AGGCAAGTGCAGAAC[A/G]GTCAGAGATAAAGGG | 23092 |
| rs529433088 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993421 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 23092 |
| rs529436203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937744 | TTGGTACACAACAAC[C/T]GGGTGCATCTTAGGA | 23092 |
| rs529438130 | in-del | -/AAAGG | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072412 | ACTGGAAACTATTCC[-/AAAGG]AAAGGAAATCATTAC | 23092 |
| rs529450386 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117384 | CTAGGCCTTTCTGTC[C/T]GGGATACATAGAGAT | 23092 |
| rs529456110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131046 | CTGACCCTTGGGACT[A/G]TGGCTCTTGCCCATG | 23092 |
| rs529463360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878478 | ACTCTTCTTTGTTTT[A/G]GGGATAGTGGTGGCA | 23092 |
| rs529464328 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032568 | CAGACTTTTTCTGTC[A/G]TTAGCAAACGCAGCT | 23092 |
| rs529470536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000012 | TACATGAAAAAGTAT[A/G]CATCATGGATCATCA | 23092 |
| rs529471354 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092737 | TCAATTATTCTTTGC[G/T]ATTAATAAGACCTCG | 23092 |
| rs529473063 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849495 | CCTCCTCCATTGACA[A/G]TGTGCTCTCCATGCT | 23092 |
| rs529476942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988114 | ATTTGGCTGTGAATC[C/T]GTCTGATCCTGGACG | 23092 |
| rs529489075 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856138 | GTGTACGAGACTGAC[C/T]TGGTCCCTGTCTTCT | 23092 |
| rs529507543 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089864 | CTTCTCTCGCTTCAC[A/G]ATGTCTTATTTTTTT | 23092 |
| rs529516615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993104 | CTCCTGCCTCAGCTT[C/T]CTGAGTAGCTGGGTT | 23092 |
| rs529519423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945020 | CCTCTCACCTGGGCT[A/G]TCCTCATTCACCAGG | 23092 |
| rs529521437 | in-del | -/A | 0.303438 | 0.244222 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088470 | TTGGACCAAATTGTT[-/A]AAAAAAAAAAAGTGG | 23092 |
| rs529524899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814180 | TTTGGGGAAGAATTT[A/G]TTGATAGTAAAAGTG | 23092 |
| rs529532685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910473 | GCCGGATGTGGTGGC[G/T]CACGCCTGTTAATCC | 23092 |
| rs529534790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137327 | ATAGAAACTCAAGTT[C/T]CTTTCCTCCACTCAA | 23092 |
| rs529539471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215505 | TTACCCATTTAAAAT[A/G]TACAATTCAATGGTT | 23092 |
| rs529544254 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772436 | AGGAATTTTGATTGA[A/G]CCTCAGGCTGGCTTT | 23092 |
| rs529552012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862516 | CAGTATTTTCCTTTT[G/T]TAATATGTATGAAGA | 23092 |
| rs529553561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952958 | TTGTGATCCTCCCAC[C/G]TTGGCCTCCCAAAGT | 23092 |
| rs529553877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855532 | GCCTGTTATGCACTA[C/G]GCCTATATCCATGCA | 23092 |
| rs529563241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040859 | TGCAATCAGAGGTAG[C/T]CAGTGCTCGATAGTA | 23092 |
| rs529566272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130517 | AAATCCATGGCTCAT[A/G]GGTTATATGAGCTCC | 23092 |
| rs529568457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861706 | TGAGTGTTTGCTGCC[A/G]GCCAGGCCCTGTGCT | 23092 |
| rs529575815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868779 | TTGAGTTTGACCTAG[A/G]AATGGGGGTGTGGGC | 23092 |
| rs529576119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047982 | CTCCTGAGTAGCTGG[G/T]ATTATAGGTGCATGC | 23092 |
| rs529579677 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048450 | ATTTTTAGTAGAGAC[A/G]GGGTTTCATCATGTT | 23092 |
| rs529585084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960578 | ACTATCTGAGGTTTC[A/G]GGCATCTACTGGCGT | 23092 |
| rs529586289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176813 | ACCATAAAAGAGACT[C/T]GGGTGTCTGATTTTC | 23092 |
| rs529588727 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228816 | CTTTGTCCCTGTTAG[C/T]AGCCCTGTTGCCATG | 23092 |
| rs529592468 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115785 | TATATGTGAGGAAAC[A/G]GGTTTAGAGAGGCCA | 23092 |
| rs529596731 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774219 | TTGAATATTACTCAT[A/G]CAAACATAAATGACA | 23092 |
| rs529598047 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168530 | TGAGTGTCACACAAG[A/G]TCTTACGACATTCTG | 23092 |
| rs529603397 | in-del | -/CATTC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904145 | CTCCTCAACTCATTT[-/CATTC]CATTCCAACACTTGA | 23092 |
| rs529604977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221700 | GGTAGTTTTTGTATA[C/T]TTTGTAGAGACAAGG | 23092 |
| rs529609088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776512 | TATGTAGTCTTATGC[A/G]TCTGGCTTCTTTCAC | 23092 |
| rs529612639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051679 | GTTATGAGCCTTGCC[C/T]CATCAGTGCTATAAA | 23092 |
| rs529618369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817180 | TCTCTCCCCAGTGCC[A/G]GAAATCAGGAACTCA | 23092 |
| rs529657821 | snp | A/G | 3.29565e-05 | 0.00405921 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142913290 | ATGTGGAAGCAGTAG[A/G]CAGGTGAGTAGCTAG | 23092 |
| rs529670187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185835 | GAGCAGAGGAGTGAA[G/T]CTTCCCAGCCACACT | 23092 |
| rs529672993 | snp | A/T | 0.0119091 | 0.0762411 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769032 | GAATTTAATACATTA[A/T]TTGCTTTCTTAATAT | 23092 |
| rs529675222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141452 | GGAGCGTGGCCCATA[C/T]GGGATATCTGTGTGC | 23092 |
| rs529679280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823823 | AAAGGCAGTCTTTCC[G/T]TAGGCTACTTCTGTC | 23092 |
| rs529692032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143009712 | AGATACTTGTTGGCA[C/T]GGATCTTTAACAAAT | 23092 |
| rs529701983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878636 | TGTTGGTAGTCAGGG[A/G]AGGCCTCCCTAAAGA | 23092 |
| rs529715069 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011896 | CAGTAGTAGAGTCCA[A/G]AGCGCTTGCATTGTG | 23092 |
| rs529715693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153228 | CTGAGGCAAACAAGA[A/C]AGGTGGCTCAAATAT | 23092 |
| rs529730123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180023 | GTGGCACCACACTCT[C/T]GAAGTTTTCTGGACA | 23092 |
| rs529733719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783197 | GTGTTTGCATTACTG[A/C]AGGCCTAGGAATGAT | 23092 |
| rs529738838 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982178 | TACACACACCTCCCC[A/C]TCCCCCAAGGCAAAG | 23092 |
| rs529740333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871858 | AACGAGGGAGAGATC[A/G]GAGACTGTTGGCTCC | 23092 |
| rs529757573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147145 | ATCTTGATCCAGTCT[A/T]ATTCTTTATACATTT | 23092 |
| rs529757681 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034260 | GGTGTATACTCAAAA[G/T]AAATGAAAATACCAG | 23092 |
| rs529760658 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853730 | CTCAGAGTAGCCTTG[A/T]CTCCACGTTCTCAGA | 23092 |
| rs529766949 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970009 | AGGCAGAAAGGAAGA[A/C]TACAGCATTTTATTT | 23092 |
| rs529771856 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970587 | GGAGTTGGGTCACAT[G/T]CCCATTCCTAAGCCA | 23092 |
| rs529775973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192704 | GAGGAAACCCAGCTA[C/G]CTTAAGGGAAAAAAA | 23092 |
| rs529791019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963365 | TATATATTCTTTTGG[A/G]TGTATACCCAGTAAT | 23092 |
| rs529791593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | ARHGAP26 | GRCh38.p7 | 5:142919399 | CCCTTGATCTTGAAC[C/T]TTTAGCCTCTAGACC | 23092 |
| rs529793636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193403 | CAGGTATACAGCCAC[C/T]AAACCTGGCTAATTT | 23092 |
| rs529794888 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066516 | CTTCCATAAATGTTA[A/T]TTTCTACAATCTGTT | 23092 |
| rs529800887 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795360 | TTGACTCTTTACCAC[C/T]GCACAGCATGCTCTA | 23092 |
| rs529804330 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038278 | AGGACTGTGAGGCAT[G/T]AAGTAGAGGGAAGAG | 23092 |
| rs529811023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977589 | GCCTCCAGTCTTTGC[A/G]TTGAACTCAGCAGTT | 23092 |
| rs529812267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805274 | CACCTGGCTAATTTT[A/G]TATTTTTGGTAGATG | 23092 |
| rs529815042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050825 | TGGGAGCTAGCAATA[C/T]GGCTACTAATCACAA | 23092 |
| rs529821984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892101 | TTGAAATTTCCCTGC[C/T]TGGAGTAAACTGTTG | 23092 |
| rs529824096 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213140 | ACAGAGCAAGACTCC[A/G]TCTAAACAAACAAAC | 23092 |
| rs529832089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058567 | GGAGCACAAGAAAAG[A/T]ATGAGAGCATAACAG | 23092 |
| rs529837691 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981243 | CTACCCACTAGTATG[A/G]TATTAATTCACTTTC | 23092 |
| rs529843425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100813 | ACTCAAATAGAGGCC[A/G]TGCACGGTGGCTCAT | 23092 |
| rs529850249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991046 | CTTTTTTTCAGCTAT[A/T]CCCTGCCCCCAGAGG | 23092 |
| rs529857505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927077 | TAGTCTGCCGTGGTT[A/T]TACATCTAGGAAGCA | 23092 |
| rs529858174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166709 | TATGGACTGGAGACC[G/T]TGAGGCAGGGGATTC | 23092 |
| rs529860001 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991359 | TTCCAGGTACCATCT[A/G]TCACAGCTTCCCTTG | 23092 |
| rs529877778 | in-del | -/CTTCT | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990176 | TCTTTTTTCTCTAAA[-/CTTCT]CTTCTCGCTTCATTT | 23092 |
| rs529888891 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780289 | TTCCAACCTTTCACC[A/G]TTGCAAGTAATGTTG | 23092 |
| rs529899881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996560 | TTTCTGTTCAATGGC[C/T]TTGCTGTCACCTAAC | 23092 |
| rs529910284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853396 | AGGTTTCACCATGTT[A/G]GCCGGGCTGGTCTCA | 23092 |
| rs529914654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089016 | TGGAGCAGGTAATTG[A/T]AAAAGGTTGCTTTAC | 23092 |
| rs529915448 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148708 | CTGGGCTTGCCTAGG[A/G]AGCCTCCCTGCCTTG | 23092 |
| rs529922655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853005 | ATTTCTCAAGCTTGC[C/G]TTTATCGAGCTCCAA | 23092 |
| rs529922754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859588 | ATGCAGAATCACTAG[A/G]ATTATACAATCCATA | 23092 |
| rs529934249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142016 | AGGTGCTGCAGGGAG[C/T]CAGTCTGTCCACACA | 23092 |
| rs529946394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134799 | TCCATTTGCTCATCT[A/G]TAAAATAGGGATAAT | 23092 |
| rs529955774 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147142 | GAGATCTTGATCCAG[G/T]CTTATTCTTTATACA | 23092 |
| rs529957675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219046 | AAGTGCGTATTCGCA[A/G]AGGGTCTGCCACCTG | 23092 |
| rs529957985 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801443 | TCTCTTTTTTTTTTA[C/G]ATGAGGAAAGACATG | 23092 |
| rs529964342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037780 | TATAGGTTAGTGAAG[A/T]TAAAGATGTAATTGT | 23092 |
| rs529966380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906713 | AGTCTGTAAGAATAC[A/C]CTAAGATGGTTTGTA | 23092 |
| rs529978226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088565 | AGAACCCAAGATAAT[C/G]TGAGACTGAAAAAAA | 23092 |
| rs529978439 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769432 | CAGAATTGAGTCCTG[C/T]GGTCGAACAGAGGGA | 23092 |
| rs529981306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996024 | AGGGAGGGAACATAA[C/T]ATACCGGGGCCTACT | 23092 |
| rs529986040 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142859036 | AGTGGGGTGTGCAGA[C/T]GAGGTAGATTTTGTA | 23092 |
| rs529988680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812012 | AGCTTACTCATCACC[C/T]AGCTGCTGTGATGAG | 23092 |
| rs529992876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052198 | GCTCTTGGGCCAGGC[A/G]CGGTGGCTCATGCCT | 23092 |
| rs529993866 | in-del | -/ACTA | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015279 | TTGAAGTCAACTCTG[-/ACTA]ACTGAGGCAAAAACA | 23092 |
| rs530005846 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990044 | GATAATATCCTGCAG[A/G]GTGTTTTCCAGCTTG | 23092 |
| rs530008932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127823 | TAGAAGTCGCATTTT[A/T]TTTCTTTGATATTTC | 23092 |
| rs530031825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179202 | TAAATACATGATTAT[C/T]AGACATTAATATACC | 23092 |
| rs530032149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173419 | AGTGGAGTCAGGAGA[C/G]CGGAAAATCACCACA | 23092 |
| rs530039134 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932794 | AGGCCATGGGCTCCA[C/T]TGACTATAGAACTCT | 23092 |
| rs530043345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172437 | AAGAAGGGAAAAAAT[A/G]TAATGGGATGTATAG | 23092 |
| rs530045978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180346 | GGCCAGGATGGTCTC[A/G]ATCTCTTGACCTCGT | 23092 |
| rs530053051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817736 | AGGAGCAGTCATTAC[A/G]TCTGTGCTCGCCAAA | 23092 |
| rs530067459 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087572 | TCTCCTCCTCTGACC[C/G]TAGGGCTTTTGTCTG | 23092 |
| rs530079088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857431 | ATTCCTGTCTCTGCT[A/G]AGGGCTCCTGGGTAC | 23092 |
| rs530091629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093573 | GTGTCTCTCTTTCTC[C/T]CTCTCTGCCTCACTC | 23092 |
| rs530094845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948025 | AACATAATCATACCT[G/T]GTGTCTTAAACAAAA | 23092 |
| rs530103248 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171918 | TTCCTCTGCATTTTT[A/T]TTTGTTTCCTTCCTT | 23092 |
| rs530104528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856893 | ATCCCGAGGGACAAC[C/T]GTACCATGAACTGGG | 23092 |
| rs530114384 | in-del | -/TCTG | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111305 | TATTGTATCTCTCCC[-/TCTG]TCTGTCAGTCTCTCT | 23092 |
| rs530121500 | in-del | -/CCCACCCTTTC | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059553 | CTTTCTCCTCCTTTT[-/CCCACCCTTTC]CCCACCCTTTCCCCC | 23092 |
| rs530127191 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886009 | AAAGTAGTTCACTTG[G/T]AAAGAAAAATGATGG | 23092 |
| rs530140712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080923 | CTAGGGTAGTAGTGG[C/T]GGAAATGCTGAACAG | 23092 |
| rs530163124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863772 | TGCTGGATCACATGG[A/G]AATTTTGACAAGATC | 23092 |
| rs530172567 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223987 | GGACCGTCAAGCTCC[C/G]CAGGAGCCCCTTGGA | 23092 |
| rs530176452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001609 | GGGAGTAAATGTGCT[C/G]TTCTGGCTGGCCTAA | 23092 |
| rs530183862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946443 | GTTGGATTAGCTTCA[A/G]TTTTTTTTTTCTTTG | 23092 |
| rs530184313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815744 | TTCAGACTCATTCGA[A/G]CCTCACTTTCCCCGG | 23092 |
| rs530184682 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976987 | CAGGGCAGGCTCTTT[C/G]ATTGGCCTGGGCCAG | 23092 |
| rs530189613 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065249 | GTTCTTCATGAAATG[C/T]CTCTCTTTTTGGCTG | 23092 |
| rs530200959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114111 | ACTGTGTAGAAGTAC[C/G]CACCATAAGCATTCA | 23092 |
| rs530201437 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042333 | TACTGAGCAGGTGTC[A/C]TGTAACTCTCAGATA | 23092 |
| rs530203827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809873 | TGCATTTGGTTCTGG[A/G]AATACAGCATGAATA | 23092 |
| rs530207765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022783 | GCACAGTTGAGAAGT[A/G]GTGAAGCTCATACTC | 23092 |
| rs530208515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905527 | TAACATTTAGCCACA[A/G]TGATATCATTCCTTC | 23092 |
| rs530210395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139699 | ACTCACGCTCATTTG[C/T]GATCACCTTCGAACA | 23092 |
| rs530213942 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956262 | TCTGTGTCCTGGTCT[A/G]TCTCTGAATGACAGA | 23092 |
| rs530217697 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995236 | AACAGGCAACCTACA[A/G]AAAGGGAGAAAATGT | 23092 |
| rs530222792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132579 | TAATGTTAGATGAAA[C/T]TATATGATACAAACA | 23092 |
| rs530224456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216719 | CTGGTCTGCTTTTAA[C/T]CAGCCTTGCCAGTGA | 23092 |
| rs530242425 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015941 | TAAAAAAGTGACCAC[C/G]CTCTAACTCCCCAAT | 23092 |
| rs530242627 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910707 | TGGCGCCATTGCATT[A/C]CAGCCTGGGCGACAG | 23092 |
| rs530245582 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912013 | ATGTAGCCACACTTT[C/G]TGTTATTTCAACAAA | 23092 |
| rs530248386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789537 | CATCCCAACCCATCT[C/T]ACTACCCAGAGGTGA | 23092 |
| rs530264837 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835851 | CTTACAGTGATCTCA[A/G]TTAGATTCTATTTGT | 23092 |
| rs530267350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884437 | TGAAGACAATAATAC[A/G]GCTAATAATTTCTTA | 23092 |
| rs530296786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926600 | GTAGGCCACTTTGTT[A/G]CGTTACTCAGGAGGA | 23092 |
| rs530297822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851966 | ACACAGTCCCTCCCC[A/G]GTCTTGGAAAGATGA | 23092 |
| rs530298714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212203 | CTCAAAACCTGGTCT[C/T]TGAGACCCTGGCTAA | 23092 |
| rs530299619 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844584 | TAAGAACTCTTTTAG[G/T]CTGGGCGTAGTGGCT | 23092 |
| rs530317844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984083 | CCTTAGAGTGAGGAG[G/T]ATCCTTTAGGATGTA | 23092 |
| rs530323625 | snp | A/C | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864856 | GGCCACACAGCTGGG[A/C]AGTGAGAGACCGGGA | 23092 |
| rs530327344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837284 | GTGGAGGATACTCTA[C/T]TGGAAAGTTCTGTTC | 23092 |
| rs530335008 | snp | G/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862638 | GGGTTCTGTCTGGGT[G/T]CGTGGGCCCTGACTG | 23092 |
| rs530336471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072707 | TCGATCTCATAGAAG[G/T]AAAAAGTAGAAGAGA | 23092 |
| rs530338578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890415 | CATGTCACCATGCTG[C/G]AGCATGGTGACAGTG | 23092 |
| rs530340378 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993050 | GCAGTGGCGGGATCT[C/T]GGCTCACTGCAACCT | 23092 |
| rs530351179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983407 | GACAGGTTTACACCA[C/T]GTTGGCCAGGCTGGT | 23092 |
| rs530351645 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808007 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 23092 |
| rs530357026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990435 | AAGTTTATTCTTACC[A/G]ATCATCTCAAGCCTT | 23092 |
| rs530378750 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040002 | GATTGCAGTGTGTGT[A/T]TGTGCATACGTATTT | 23092 |
| rs530382811 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186815 | ACAGGAAGTAATCCT[A/G]GAATGAAAGCTCTAG | 23092 |
| rs530391563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987293 | ATGATTTGGCTCTCT[A/G]TTTGCCTGTTATTGG | 23092 |
| rs530392856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040610 | TTCAGATATTGTTAA[A/C]TGCTATAAAGAAAGA | 23092 |
| rs530395516 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948805 | TTTTGTGTCCATATG[A/G]TAAGAGTACATTAAA | 23092 |
| rs530396795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123282 | GGGTTTGTCGTCTTT[A/G]TGAGAGCAATTGGAA | 23092 |
| rs530408763 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976081 | AGAAATTCTCACTCT[A/C]TCTGGATTTTGCCTT | 23092 |
| rs530410068 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176345 | ACGTTCACTTCTTAG[A/C]TGGTAGGAATTAATC | 23092 |
| rs530412399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804664 | ACCCAGCTAATTTTT[G/T]TATTTTTAGTAGAGA | 23092 |
| rs530415014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036592 | CCTGAGCAGGATTAT[A/G]CTTAACTCAGGGACA | 23092 |
| rs530415305 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833211 | GGCACCCACCACCAC[A/T]CCCGGCTAATTTTTT | 23092 |
| rs530416159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176686 | CATTTTGGAGCCTGC[A/G]GAAGGAATTACTTTA | 23092 |
| rs530416691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029938 | TCCTCTCCTTTGGAT[A/G]AGGATTTCCCTCCCC | 23092 |
| rs530420290 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167927 | CATTAAAGATGAGTT[A/T]CAGGGGATCGTGCCC | 23092 |
| rs530422359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944858 | CTAAGTTTCGCTTGT[G/T]TTCTTTCCTTAACTG | 23092 |
| rs530431966 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854937 | GCTGTTCAAAGGACC[C/T]CCCAGTCCCTTTTGT | 23092 |
| rs530455083 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853750 | ACGTTCTCAGATGCT[A/G]TAGGTCCTTCTCAGT | 23092 |
| rs530481415 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033240 | TAAGACTTAATTCCA[A/T]GAAAAGGAGTTTGCT | 23092 |
| rs530493204 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854360 | AGTTTTACATTCTTG[C/G]CACTGAAATTTTCAG | 23092 |
| rs530494516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860931 | GGGAAGCCCAGGCTC[C/T]TAGGCCTCAGCCCTA | 23092 |
| rs530495633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894721 | ACCCTTCTTCTCTTC[C/T]TCAAATAATTCAGAT | 23092 |
| rs530522635 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033835 | TCTTAAGCACCTCTC[A/C]AAAGAAGAACTAAAA | 23092 |
| rs530526864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161876 | TGGAAAGCCCTGTTC[A/G]GTCTATTTTGTTTAC | 23092 |
| rs530530503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958837 | GCTTTGGGAGGCCAG[A/G]GCCAGAGGATCACTT | 23092 |
| rs530530540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951312 | TGATCCGCCCGCCTC[C/G]ACCTCCCAAAGTGCT | 23092 |
| rs530531258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214404 | TTTAAGAGATCATAC[A/C]CATCACATGTTTAAA | 23092 |
| rs530535169 | in-del | -/CAGTCTGGAGGCAAC | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876579 | CTGGGAGTTCAAGAC[-/CAGTCTGGAGGCAAC]ATAGTGAGACCCCAT | 23092 |
| rs530559424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931473 | GTAAAGCACTTAGCA[C/G]CTGACATGATTAAGT | 23092 |
| rs530567851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820167 | TTAGATGAGGAGTGC[A/T]GGTGGTTCTCAGACC | 23092 |
| rs530578715 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784977 | TGTTGTCCAGGCTGG[A/G]GTGCAGTGGCGCGAT | 23092 |
| rs530579224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951335 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA | 23092 |
| rs530586781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110890 | ACTGTCCAGGATGAG[A/C]TAGGTGAAAGCTAAT | 23092 |
| rs530588027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118034 | TGTAATAAATGCAGG[A/G]GCAGGCCAACACTTC | 23092 |
| rs530601920 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156235 | ACTGCTTTTGAAACC[-/TT]TTTTTTAGTCAATCT | 23092 |
| rs530601988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142771793 | TTTTTTCCTTTTGGT[A/C]CAAGGGGAGAGATGC | 23092 |
| rs530606720 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128440 | GAGATTTTTAATACA[A/G]CTACCCAAACTACTT | 23092 |
| rs530622905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104187 | TTGACATAGATCTCA[C/T]GGGTGACAGTTTGGT | 23092 |
| rs530623644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046763 | TATGTCTATCTCTCT[C/T]CCTGTCTCTCCGTAC | 23092 |
| rs530624727 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111683 | AGAGCTATTAAATGT[A/G]CTGAAAGGATCCTGG | 23092 |
| rs530637491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842377 | GGTTTGTGGCCGCTT[C/T]TTCCATTCCTTCTAC | 23092 |
| rs530642256 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009745 | TCATATACAATGGTC[A/G]GTAGAAACTAGACTA | 23092 |
| rs530650534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881477 | AAAGAATTTAAGTAG[G/T]CACTCACCAAAGCAT | 23092 |
| rs530652281 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043817 | GCTGTAATGTAAAGT[A/G]TGATATTCATGCTTA | 23092 |
| rs530652558 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080547 | AGGTAGAGGAAGGTT[C/T]CTCCAGGAAGAGGGA | 23092 |
| rs530659391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040162 | AGCCCACAAGCTGAC[A/G]TGTTACTGAATCAAG | 23092 |
| rs530669822 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185739 | ATGTTAACTCCTGCA[A/G]TCCACACAAACACCC | 23092 |
| rs530670087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998293 | GGAGCAGGGCTGAGT[A/G]GTAGGGCCAAGGAGA | 23092 |
| rs530677031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937530 | CTCTATGACACAGCA[A/G]TTGCTCTGGGGCATT | 23092 |
| rs530678090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813037 | CCGCCTCCTGGGTTC[A/C]CGCCATTCTCCTGCC | 23092 |
| rs530683102 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820766 | TAAAACATAAGAATG[A/C]AACATTTTTAAGCAA | 23092 |
| rs530684193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973625 | CTTATTGGTTATGAA[G/T]GAAAGAGAAATTTCA | 23092 |
| rs530688247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077910 | AGCATATCTCCCCTC[C/T]CCCAACCCTGGTTTC | 23092 |
| rs530691951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867701 | AGGTTTTATTTTATG[C/T]TCCTGCTGGTGGTAG | 23092 |
| rs530707024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156332 | TAACTCCTTCTCTGC[A/G]TTAGGGATCTGGAAA | 23092 |
| rs530707692 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980868 | TGTGTGAGGGTTTCA[A/G]TTGTTCCATGCCCTC | 23092 |
| rs530708905 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893071 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 23092 |
| rs530711564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880927 | CCAGTTTTAGAGTAT[A/T]TTCTACTAATTTTAG | 23092 |
| rs530719051 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787091 | CTGTTATACTTCCTG[C/T]GTTACATTTCAGAGT | 23092 |
| rs530723179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895467 | GATCTCCTGACCCCG[C/T]GATCCGCCCGCCTCG | 23092 |
| rs530739507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987938 | TTGATATTCATCAGG[C/G]ATATTGGCCTAAAAT | 23092 |
| rs530743433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849205 | AACCATCTCAGGATA[A/G]TTTTCACTAGCTAAA | 23092 |
| rs530746509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:142919813 | ACCAGCCTGGCCAAC[A/G]TGGCAAGACCCTGTC | 23092 |
| rs530754792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196511 | TATGTATTTCTGCCT[A/T]AAGTCACCTCATTTA | 23092 |
| rs530761740 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037477 | AGAAGAATGTGTTAA[A/G]TATCTAAAATACGTA | 23092 |
| rs530765364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062152 | GCTAACACAATCAAG[A/G]TATATAGGACAAAAA | 23092 |
| rs530769776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156772 | AACTGAGCTCTGCCC[A/G]TGGCCTTTGGGATCA | 23092 |
| rs530792871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929030 | GCAGCCTCCGCCTCC[A/C]GGGTTCAAGCGATTT | 23092 |
| rs530794801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921492 | TTTAAACTAAACTTT[C/T]AGCAGGTGCTCACTT | 23092 |
| rs530797032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154161 | TGATTTAAAAATATT[A/T]AAAAAAAAAAAAGAG | 23092 |
| rs530799400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161031 | TTTTTTTTTTTTGAG[A/G]TGGAGTCTCTTACCT | 23092 |
| rs530805707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162311 | CACACACACACACAC[A/G]CGCAATCCCCTTTCC | 23092 |
| rs530828632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935482 | TGCTTCAGTAAAACT[G/T]TATTATTTACAAAAA | 23092 |
| rs530836227 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000184 | GGTGGGGGTGTAAGT[A/G]AAATGGCACAACTAC | 23092 |
| rs530837777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801186 | TGACTCTTTCCTCTG[C/G]GTTTGAGCTGTGGAA | 23092 |
| rs530843765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069572 | CACCTGTCTTTCTTG[A/G]TAGGACCACATGTAA | 23092 |
| rs530857465 | in-del | -/TTTTTTT | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865495 | TTTTTTTTTTTTTTT[-/TTTTTTT]GAATCCCTTATAACT | 23092 |
| rs530862575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841591 | CCTCAGCCTCCGAGC[C/T]CCAGGTCTGATGGAA | 23092 |
| rs530864462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117255 | GACCTTGCTAATGAA[C/T]GAGTCCCGTGGCCTC | 23092 |
| rs530877970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979460 | CCTGTGCATCCAGAG[A/G]CTATGGGACATATTC | 23092 |
| rs530882268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074478 | ACCTATAAGCTAATA[A/G]TTTTTCTTAACATTT | 23092 |
| rs530883502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160420 | CTAGGAGTCTAAATG[A/G]GATGCTATTTGACAG | 23092 |
| rs530892302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201513 | GGTGAGGGGCAGGAG[A/G]GAGCAAGATTTTTAT | 23092 |
| rs530896285 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115648 | ACCTCGACAGCCACC[A/G]TGACAAGAGCAGATG | 23092 |
| rs530909526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799612 | AACCAACAGAAATTT[A/G]TTGGCTCAAAATTCT | 23092 |
| rs530923137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806110 | TTTTGTTGTTGTTGT[C/T]GGAGACAGAGTCTTG | 23092 |
| rs530958843 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142879406 | GGTGCTCATCACTCC[C/T]TTGGAGAAGTTTCGA | 23092 |
| rs530965536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053933 | GTTGTCATATAAATC[A/G]GCGAGGTAATATTCC | 23092 |
| rs530981384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068119 | GCAGTGAGCCAAGAC[A/C]ATGCCACTACACTTC | 23092 |
| rs530989688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997674 | CCTCCTGCCTTGCCT[C/T]CTGAAGTGCTGGGAT | 23092 |
| rs530989714 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165501 | AGAGCTTGGGTTCTG[G/T]GGGCAGATTTACTGA | 23092 |
| rs531021985 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843446 | TTTCACTAGATTGTC[A/G]TGATTACAATGATGC | 23092 |
| rs531023307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213690 | CTGCTCCAAAAATGG[A/G]GCCCAGCCTGCCCTC | 23092 |
| rs531028932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181890 | AGAATAAAATCTAAA[C/T]TGTTTCTCATGGTCT | 23092 |
| rs531031058 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825844 | ATAGGTGTCCTTGGC[G/T]GAATCCCTCAGAACA | 23092 |
| rs531034106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869052 | ACAGAGAGTAACTGG[C/T]GTCCAGGAAAGGAAG | 23092 |
| rs531044851 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160586 | ACCTCTTAGGCTCAA[G/T]CGATCCTTCCACCTT | 23092 |
| rs531055165 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109913 | TTTTACAGTGGCCTG[A/C]AAAGTTTTCCAGGAT | 23092 |
| rs531063041 | in-del | -/AG | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852154 | TTAAAGAGAAAAGAA[-/AG]AGTGAGGTATGCAGC | 23092 |
| rs531072131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155257 | GACATGCCAGATACC[C/T]TCCCTCTGTCACCTC | 23092 |
| rs531073573 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148995 | TGCTGAGTACAGTGT[G/T]TACAAAGAGGTTGCT | 23092 |
| rs531076880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122330 | TTCAAGGCCTTCGCA[A/G]TTGCTGTTCCCAGTG | 23092 |
| rs531080787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200855 | AGGGTCTGCCACATC[C/T]CTTGTCAGACTGGGA | 23092 |
| rs531086909 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188255 | CATTTCCAGAGCTGA[C/T]CTAGAACACAATAGG | 23092 |
| rs531090024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194822 | GAACCAAATGAACAA[A/G]GGGTAAAAATCACCA | 23092 |
| rs531095389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770990 | GCTTAGCCCGGGTTG[C/T]CCGCGCGTCTGCCGG | 23092 |
| rs531095506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908089 | TCAAATATTTTTATA[C/T]GCTGAAAATTATTGA | 23092 |
| rs531117298 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860249 | CAGGCCCTTCTGAGC[A/C]TGGGACCCTGTGCAT | 23092 |
| rs531126759 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161443 | AAGTAGTTCAATTAT[A/G]TTGAGCTATATATAG | 23092 |
| rs531129626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142783 | ACTTTTTATTGCAAA[A/G]TTCATTAAGCTGCTG | 23092 |
| rs531134125 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778184 | GATATTTTTGGCCTG[A/C]GCAGTTATGTGAATG | 23092 |
| rs531137658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792740 | TGTGGAATGAGCAGC[A/G]TTGGAGGATTTGAAA | 23092 |
| rs531139191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914933 | GATGCTCATCAAATG[C/T]ACAGTTCCTAGAGAT | 23092 |
| rs531142727 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227222 | AATGTTTTGTGAGCA[A/G]CCATGTTCCCCAAGT | 23092 |
| rs531149638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825043 | TATGTAAGAACAAGA[A/G]GACCCCTCCCCTCTC | 23092 |
| rs531152687 | in-del | -/ACTG | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023072 | AGGGTCACGCATTTC[-/ACTG]ACTGGCTTCCCCAGG | 23092 |
| rs531155177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102673 | GCTCATGAAATACCA[C/G]AGGAGAAAGCTTGCT | 23092 |
| rs531161445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135867 | GTGTTCCTTTTAAAT[A/C]TCTGGCTGGGGTCAT | 23092 |
| rs531164730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829231 | TCTGTGCAGGACCCA[A/G]CCAGGTTGACCAAAT | 23092 |
| rs531174726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113411 | ATTCACAGAGCTTTG[A/G]CATCCTTGAATGAAA | 23092 |
| rs531175789 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874853 | TCTCACCAGTCCTGG[A/G]TACTCTCAGGAACAG | 23092 |
| rs531179498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867028 | TGGAAGCCAGGGCCC[C/T]TCTCTCAGTTGCTGA | 23092 |
| rs531190182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925731 | GGCAGGTTTCAGACA[C/T]AGGCTTTGAGATTGT | 23092 |
| rs531201322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993525 | GGCCAGGCTGGTCTC[A/G]AATTCCTGACCTCAG | 23092 |
| rs531213288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965411 | GATACCGCTAGACCA[C/T]GGTCCACCTGGCAAC | 23092 |
| rs531218926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777637 | AAGAAGAGTTTCGTT[C/T]AGGAAATACGGAGAC | 23092 |
| rs531225295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925124 | CTGATCATGCCTTCC[C/T]GCATGCCAGCTACCG | 23092 |
| rs531256106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872470 | TAATTTGAATGATTA[A/G]CCTAATCTGCAGGAA | 23092 |
| rs531256187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880031 | AATAATTTTAAAATA[C/T]ATATTACCCATTGTG | 23092 |
| rs531262666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784884 | ATCTGCCATTCTTTC[A/C]ATCCCTACCTCTCAT | 23092 |
| rs531268920 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960145 | CAGCAAGAAGTGTTT[G/T]CTGGTAGCAGCAGCA | 23092 |
| rs531276385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110205 | GCTGTTTCATCATAG[C/T]ACCATATATTTTCTT | 23092 |
| rs531276551 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951886 | TGGGTTACAATAACA[C/G]AAATGTATTCTCTCA | 23092 |
| rs531291269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210698 | CCTGCCAGTCTAGCT[G/T]GTCCCACCTCCCTGT | 23092 |
| rs531292571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968197 | CTCAGTTTACAGTTT[C/T]GGAAACTGAGACACA | 23092 |
| rs531308323 | in-del | -/ACACACACACACACAC | 0.0194576 | 0.0966964 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222247 | CCAAGCTTCCTTCAT[-/ACACACACACACACAC]ACACACACACACACA | 23092 |
| rs531313445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014708 | TAAGCACTCTGGTTA[A/G]TCATGATTTCCAAGG | 23092 |
| rs531318210 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803572 | AGAAATAAGCCGGAC[A/G]GAAATCTCTGTGATG | 23092 |
| rs531319176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918038 | TTTGAACAACGAATG[A/C]ACTGAAAATCAAATT | 23092 |
| rs531323734 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218385 | TGCTATGTGCAAGGA[C/T]CTAGCATGGTGTCTA | 23092 |
| rs531329131 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030385 | GATGATAATGCCTTG[A/G]TGGACAAAATGCAGG | 23092 |
| rs531339154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106630 | GGCACGTGGCACCAC[A/G]CCCAGCTAATTTTTG | 23092 |
| rs531342275 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795208 | TTGTTGCCCATTGAC[A/T]GTATGGGCATTTTAA | 23092 |
| rs531342571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029563 | GTTCACACCACCATG[A/C]CCAGCAAATTTTTTT | 23092 |
| rs531344380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021663 | GTAAAATGGGGATAA[C/T]AATACCCCTGCTTCA | 23092 |
| rs531354768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050761 | GTAGCAGACAAAAGA[C/T]GACAGGACCAGAAGA | 23092 |
| rs531356186 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198741 | TAAATCATAGAATTA[C/T]TTACCATTCCTACTC | 23092 |
| rs531369893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876393 | GATATTGAGGTTTAC[A/G]GAGGTTAAGTAACTT | 23092 |
| rs531370599 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883550 | TGGTTATTCTGCCCA[C/G]TCTGTGAGCATGTAC | 23092 |
| rs531391601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857468 | CTTCTCAGGTGCCCA[A/G]GAGAAGCTGTGTGAC | 23092 |
| rs531392765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216479 | ACTACAGCCTCATGC[C/T]TTCTTCATGTTCTCA | 23092 |
| rs531404586 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050426 | TTATACAGCAGTGCT[A/G]TAAAGCACGGAATTA | 23092 |
| rs531420830 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773989 | TTGCAATACATAAGC[A/G]CTTCTTGAATGGCAT | 23092 |
| rs531421275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204577 | CATGGGGATTGAGGA[G/T]TAAGTTATTATAATA | 23092 |
| rs531425351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975222 | CTTGGAAAAGCTGCT[C/T]ACCCCTCCTAGGCCT | 23092 |
| rs531425842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119056 | ACATTCACATGTGCC[A/G]TGCCATTGTGTTCTC | 23092 |
| rs531429850 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901056 | AGAACTTGAGAAGGG[A/G]CCAGGAAAGCATAAC | 23092 |
| rs531443851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140609 | GAAATATCCTTCCCT[G/T]TGGAGCCTGCAGATT | 23092 |
| rs531483718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205130 | CAAGACAGAGTCAAG[A/G]GGGAGCCAGGTATTA | 23092 |
| rs531485544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043001 | CATTTTGAGATAATT[A/G]TAGATTTACATTCGG | 23092 |
| rs531486950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962405 | ATGAAAGAATAGGGG[A/G]AAATAACAAGAACTG | 23092 |
| rs531495643 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852954 | AGAGTCTCTCTTTTG[C/T]AGAGGCCTGCTGCTT | 23092 |
| rs531504274 | snp | A/C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091182 | GCGCTTTCTTGACTC[A/C/G]GGTGTGATGAGTCCA | 23092 |
| rs531504747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905717 | ATCTGTTAGGTTGGT[A/G]CAAGAGTAATTATGG | 23092 |
| rs531508060 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850535 | AGACCTATACTTGCA[C/T]ACAAACTTTCGAAGT | 23092 |
| rs531508856 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994762 | GTTTACTGAGCATTT[A/C]CTCTGTGCCATGCAT | 23092 |
| rs531508956 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002527 | GGGTTCACATCCACT[C/T]TTTAATGTTGCATCA | 23092 |
| rs531510393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093627 | CTTTGTCTCCTCCTC[A/T]CTCTCTCTGCCTCTT | 23092 |
| rs531510501 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062921 | TCCAAATAAAATAGC[C/T]GTAGAATTTTACAAA | 23092 |
| rs531511257 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121324 | AGGTTGGTGGTAAAG[G/T]TGTCAACCGTGGTAG | 23092 |
| rs531514690 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985985 | TGTGTATGTGTTTTT[A/G]TAGCAGCATGATTTA | 23092 |
| rs531523392 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228169 | TAAAAGCAGCTTTCT[C/T]GGTTATCCAGATGCC | 23092 |
| rs531532335 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146996 | TTATATTAAAGGGGA[A/G/T]ATATATCCTGTTATG | 23092 |
| rs531546052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009534 | TAAGACAATGCACAC[A/G]GAATGCTTGGCATGA | 23092 |
| rs531552600 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224010 | CCCTTGGATGGCAGC[A/G]TTGCTTCAGAGTGTT | 23092 |
| rs531561903 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773196 | AATGTTTGTGTATTA[G/T]TTTTCTTCAGTCATG | 23092 |
| rs531571766 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000198 | TAAAATGGCACAACT[A/G]CTGTCGACAAAGGCT | 23092 |
| rs531576281 | snp | A/G | 0.0410537 | 0.137264 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963204 | TATATATATATGTGT[A/G]TGTGTGTGTGTGTGT | 23092 |
| rs531594834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146474 | GCCTGAGGCCACATA[A/G]CCAGTCAGGGCTTGA | 23092 |
| rs531598082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780619 | CAAAAATCATTCCCT[A/C]AACTGAGACAGCTGT | 23092 |
| rs531608030 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933530 | ATTTCTCTCTTAGAG[A/C]CGAGAAGGGAGGAGT | 23092 |
| rs531611975 | snp | A/C | 0.00676609 | 0.0577691 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229360 | TGAACACAAGGATGG[A/C]ATCATCAGAGCCAGA | 23092 |
| rs531617484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196002 | TTTAAAAGTTACCTT[C/T]AATCTCATCACCCAG | 23092 |
| rs531624584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782255 | ATGCAGGTGGAGACA[C/G]CCACAAGGCTGTGGG | 23092 |
| rs531629946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098683 | ATCATGGATCTGTTC[C/T]TTCTTAGCTAGGTGA | 23092 |
| rs531655873 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776193 | GCCCAGGCTGGTCTC[A/G]AACTCCTGGTCTCAG | 23092 |
| rs531658337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013785 | TAACTAATTTTAATT[G/T]TTTTCTCTTTTCTAT | 23092 |
| rs531662506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869975 | AGCACAGCCCTACCT[A/G]CTCTGGAAAGCAGAT | 23092 |
| rs531675846 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223490 | ATGCTGCCTCCCAAT[A/G]GGTGATGCCATCTGA | 23092 |
| rs531677707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107221 | GGGTAGTTAGAGCTC[C/T]GTGAATAAGAGCATG | 23092 |
| rs531681666 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116632 | TGGCTACTGCTATTC[C/T]CATCATAATGCTCCC | 23092 |
| rs531689863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143063075 | ACTGAACACCGCAGT[A/G]CTGCCAGTGCAGGAT | 23092 |
| rs531695703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814258 | ACACCATGGCTAGAG[A/C]CTTCCGGTAATCTGC | 23092 |
| rs531703203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821666 | ATTTTAACAAGATAC[C/G]CAGGTGATTTATCTA | 23092 |
| rs531720399 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228888 | TATAAAGAAAACAAA[A/G]TTTCTGTTCAGAGGC | 23092 |
| rs531723892 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111527 | TGAGGGAGTGGTTAT[C/T]CCTGGCTCACAGTAA | 23092 |
| rs531739291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142910051 | AAAAATTTTTTGGAA[C/T]AAATCCTGACACATA | 23092 |
| rs531740381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786851 | GGGGTTTCACCATGT[C/T]GGCCAGGCTGGTCTT | 23092 |
| rs531744153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177488 | TGGCAGAGCTGGCAC[A/G]TCAGTAGCAGACACG | 23092 |
| rs531745711 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092254 | CTGCAAGCTCCGCCT[C/G]CCAGGTTCACGCCAT | 23092 |
| rs531747206 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021495 | CATCAGCCTTTGTAC[A/G]TATCTCAGATCATTC | 23092 |
| rs531762223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125557 | GTGTTTGGCACAATT[C/G]TGGGAAATAAATATC | 23092 |
| rs531769673 | snp | A/C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884436 | TTGAAGACAATAATA[A/C/T]GGCTAATAATTTCTT | 23092 |
| rs531775051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035367 | CTGAGCTATAAAAAG[C/G]AATGATTAATGGCAT | 23092 |
| rs531777158 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989205 | ATATATTTAGGATAA[G/T]TAGCTCTTCTTGTTG | 23092 |
| rs531779546 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861896 | CTGGATGAAGGCCTC[C/G]ATTTACCCACCATAC | 23092 |
| rs531780995 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118780 | TTGATCACACACCGG[C/G]GACTGTTGTGGGGTG | 23092 |
| rs531793873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868857 | TCTGTCATGGGTCCT[C/T]TCTGGAGACTCTCAG | 23092 |
| rs531795318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150611 | AGGGGAGGAGGGAGC[C/T]GGAATTCCTCTGGTA | 23092 |
| rs531810898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938870 | TTAAATAAAATATTT[A/C]TCCACTTTGAGCTGG | 23092 |
| rs531813209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993892 | CCCAGATCAGTCTCA[A/G]ATTCCTGGGCGCATG | 23092 |
| rs531813809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803042 | TAATCCAGCCTCATG[C/T]GCAGACTGTCATAAA | 23092 |
| rs531818424 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054987 | TTTTGACTCCTTCCC[G/T]TACACTGGACAATAT | 23092 |
| rs531822907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960080 | GTCATGGCCTCATGG[C/T]CATAGCTGAAGCTGT | 23092 |
| rs531838438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143222256 | CTTCATACACACACA[C/T]ACACACACACACACA | 23092 |
| rs531843018 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064609 | TTTAAAGGGACATTG[C/T]ACAGAGCACAACGAC | 23092 |
| rs531853727 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147153 | CCAGTCTTATTCTTT[A/G]TACATTTTTGTGCAT | 23092 |
| rs531861487 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028747 | CAGGGTTCTAATCCA[A/G]GTCTGTCTGGCTTTA | 23092 |
| rs531864630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896578 | TTCTTCTCCTTCTTT[G/T]GTCTCTCCTCCCCCT | 23092 |
| rs531866439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904705 | CAGACTTAATTCGTG[C/T]ATGCAATGCTAGGAA | 23092 |
| rs531877739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916222 | AGTGTGAAGTATGTG[A/T]CTTAGAATATGGGAT | 23092 |
| rs531883914 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827498 | TGGTGGAGGTTGAGG[A/T]TGGGGCAACATGACC | 23092 |
| rs531887866 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924066 | ACGGGGTTTCACCGT[A/G]TTAGCCAGGATGGTC | 23092 |
| rs531890869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131781 | CATCTGCCTAGCATA[G/T]TGCCTGGTAGGTGCA | 23092 |
| rs531901182 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809129 | AGTGTTAAATTTTAT[A/G]CTGTAGAAATGTTGA | 23092 |
| rs531906156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210251 | TCTTTCATGGATGGC[A/G]GCAGGCAAAAAGAGA | 23092 |
| rs531907089 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857108 | ACAGGGCCTTCTTCC[A/C]TGGGTGTGTGTGTGT | 23092 |
| rs531907434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138876 | TAAATAGTGTACGCT[C/T]AGGGTTACACGGCAA | 23092 |
| rs531907589 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982313 | TGAAACATGGGCTCA[-/T]TTTTTTAATGAGAAC | 23092 |
| rs531907679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215658 | CCAGCCCAAGGCAAC[C/T]ACTCTTCTACTTTGT | 23092 |
| rs531907726 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909318 | CAAGCATTCCACTTC[A/G]GTCCTCTCTGCAGTA | 23092 |
| rs531907984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809718 | TCTGCCAGTCCTGCT[A/G]GAGCCATCCACTCCT | 23092 |
| rs531920390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000724 | GAGGTCATGTCCTTT[G/T]CAGGGACATGGATAA | 23092 |
| rs531922950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843272 | TTCCCAAGCATGCAG[C/G]TGAGGCAAAGAGTGT | 23092 |
| rs531924583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903878 | GAATTCCTTTGGGAA[A/C]CTGCAATTCTTTAAG | 23092 |
| rs531933839 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850792 | TGCAGAGCCCTGTGC[C/T]TCATATGTAGCAAAT | 23092 |
| rs531941500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041997 | CAAAGGAATCGGGGT[A/G]TCCGTGAGCTGTCAC | 23092 |
| rs531941569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163618 | ACCACACCCAGCTAA[C/T]TTTTGTATTTTCAGT | 23092 |
| rs531944438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850152 | CTCCTGCTCTGCCTA[C/T]GGCTTGTCCCCTTCT | 23092 |
| rs531947118 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142770178 | GCTGGGAGGGCAAGA[A/G]GAGGCGGAGTTTGCG | 23092 |
| rs531950619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856705 | AATACAGTATAACAA[C/T]GATTTACATAGCATT | 23092 |
| rs531956408 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786635 | GAAATGACGTGAAAC[A/C]GATTTCTGGAGTTCT | 23092 |
| rs531976051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812085 | TTTTGTGAAAGGCTC[C/G]CCCTCCCCACCCCGT | 23092 |
| rs531977205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946235 | TGTATCTTCTACCCT[A/G]TCTACTCACATCATA | 23092 |
| rs531983817 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769469 | GGCAACGCACTGGGC[C/G]TGGGAGGTGGAGATG | 23092 |
| rs531992517 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095748 | CAGCTAATTTTTGTA[G/T]TTTTGGTAGAGATGG | 23092 |
| rs531993877 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142771088 | GGCGAACCAGCAACC[A/G]TCAGATGAAGAGAGA | 23092 |
| rs531994039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085523 | ATTAGCTTAGGAGAA[C/T]GCGACAGAGGCAATA | 23092 |
| rs531997066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096394 | ATATTACTGTTTTCC[C/T]TAAAGTAGACACTCA | 23092 |
| rs532001518 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060557 | GACCTCAGAGGGAAC[A/G]TAAAAATTATAGGCA | 23092 |
| rs532015408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954107 | GCGTTCTAACCCCAC[A/G]GCCCATCTCTGGGAA | 23092 |
| rs532015472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856184 | TGAGCAAGTGTGAAA[A/C]GTGTTGGGAGAAACC | 23092 |
| rs532020346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041486 | TTAAAAATTGGTTAA[A/G]TATGACATATTTAAA | 23092 |
| rs532023165 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149584 | AACAAATGGACCCAC[A/G]GTACTTTCCCTGAGC | 23092 |
| rs532024886 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792108 | GTCCATATTTCAGGC[C/T]TCTCATACATTGTTT | 23092 |
| rs532027195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866192 | CCCTTCTAAAAATTG[G/T]ATTCCCCTTAAGGCA | 23092 |
| rs532028999 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882460 | CACTGTTCTGTGCCC[C/T]GATATTTGGTGGAGA | 23092 |
| rs532029179 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988796 | TTCCCTGTAGTTGAG[C/T]GGTTTTGAGTGAGTT | 23092 |
| rs532035836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048940 | AAAAAAAAAAAACCT[C/T]ACCCAATCTAGAATG | 23092 |
| rs532038698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872330 | TGTGCAGCCACAGTA[C/T]ACCCCCCCACCACCC | 23092 |
| rs532041418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216235 | CTGCCACACCGAAGC[A/T]CCGGGCACCTCCACC | 23092 |
| rs532062925 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776756 | AATTTCATTTTTTAC[C/T]TAGGAGTAGAATTTT | 23092 |
| rs532063941 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907308 | GGGAATGGTCACAAG[C/T]GCTTGGAGGAGGCTT | 23092 |
| rs532070294 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005017 | TTTCTCGTTCAACTT[C/T]GTTGCACATTTTTCT | 23092 |
| rs532074307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178096 | CCTCCGCTTCCCAGG[A/C]TCAAATGATTCTCCT | 23092 |
| rs532092385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871923 | TGGTGTAGAGCAGAG[C/T]GCTTTGGACAAACCG | 23092 |
| rs532107628 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226036 | TTGGTTATCAGAGTG[A/G]AAGACCATGGCCCAG | 23092 |
| rs532120091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859643 | TCATTCTTCCAAGAA[C/T]AGTGGAAATGTTGCA | 23092 |
| rs532128079 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187464 | GCAATTCAAGCAAAT[G/T]TTCTGGAAGTCTGCT | 23092 |
| rs532140964 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180383 | CCCACCTCAGCCTCC[C/T]AAAGTGCTGGGATTA | 23092 |
| rs532142355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914052 | TCAGCATGATACTCC[A/G]TATAATGCCATTTAA | 23092 |
| rs532181090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025040 | CATCCTTTGCTCAAT[C/G]GTGCCTGGTATTATC | 23092 |
| rs532203168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799674 | GCATCTGGTGAGGAG[A/G]GGTCTGCTTTCTGTG | 23092 |
| rs532207095 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127418 | CAAAATAAGTTATAA[C/T]AATTCCTTCCCTAGT | 23092 |
| rs532207743 | in-del | -/TTTTTTTTTTTT | 0.300926 | 0.244758 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106467 | TACAATGCATTGGGC[-/TTTTTTTTTTTT]TTTTTTTTTTTTGAG | 23092 |
| rs532221681 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817773 | TGTTTGCCCCTGCTG[A/C]AGTGATGGTGGAGAG | 23092 |
| rs532221917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051741 | CCTCTCTAATGTTAC[A/G]CAATATTCCTATGGT | 23092 |
| rs532236059 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829583 | AGGTGCAGTGTGATA[C/T]AATTGGTATTTATCT | 23092 |
| rs532240495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934957 | TACTTTTTTAATACA[C/T]AGTCATATCCTAGTC | 23092 |
| rs532243346 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124426 | ACTCTCAATTCTGTG[A/C]GTCAGAAATTTGAGA | 23092 |
| rs532247070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161085 | GGAGCGATCTCAATT[C/T]ACTGCAACCTCCACC | 23092 |
| rs532253295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892931 | CTTGTATCTCACTGT[A/G]TTTTTGAACCCATTA | 23092 |
| rs532253539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901167 | TAGGGGCTCAGGGAG[A/G]GGACATTAATAGTTT | 23092 |
| rs532255539 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794905 | GGAAATAAACTATAA[C/T]TAATAGAGCTTGTTG | 23092 |
| rs532258038 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204510 | GCCTGGGCGACAAGA[A/G]CAAAACTCCGTCTCC | 23092 |
| rs532260372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052247 | GAGGCCGAGGCGGGC[A/G]GATCTCGAGGTCAGG | 23092 |
| rs532261091 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782059 | CAGGTGTGGATGAAG[A/G]GAACACATAGTCAGC | 23092 |
| rs532269656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219827 | CCAGGAATGTGCAGT[C/T]TGAATAAGCATCCTG | 23092 |
| rs532281165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011014 | TTGCTGGTCTTAGCT[A/G]TTACACTGTGACCCA | 23092 |
| rs532286191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128887 | CAGTTGTAGACTAGG[A/G]GCTCTTCGTCATGAC | 23092 |
| rs532289791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921317 | GCTTCCAGAGGCAGA[A/G]GAACATTTTATGCAG | 23092 |
| rs532292232 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142770181 | GGGAGGGCAAGAGGA[A/G]GCGGAGTTTGCGCTG | 23092 |
| rs532299712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032487 | TTCTGAGCCTTGGCT[C/T]AGTGAAAGAGCTGAA | 23092 |
| rs532312564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213804 | TATGGCTTTTCTCTG[A/G]ATATTTCTCATTTTT | 23092 |
| rs532313753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900613 | GGAGAGTAGGGGGAG[C/G]GGGGGCGGGATGAGA | 23092 |
| rs532319134 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914350 | CAATTTAGTCATTAC[A/G]TCTTTGGCTGTCAAG | 23092 |
| rs532325514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167368 | GCGCCTGTAATCCCA[C/G]CTACTCGGGAGGCTG | 23092 |
| rs532328471 | snp | C/G | | | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069768 | TGTTACAAATTTTAA[C/G]TCTGTGATGGATCTT | 23092 |
| rs532330047 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210139 | TGATAAAAACATACC[C/T]GAGACTGGGAAGAAA | 23092 |
| rs532332665 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031779 | AGGCTGGAGTGCAGT[C/G]GTGCAGTCTCGGCTT | 23092 |
| rs532333762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083467 | AATATTTTTTGAGTG[G/T]AGAAGAATTTCCTGT | 23092 |
| rs532333906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839414 | AGCTAATGTACAGAG[C/T]GGTCATATAACTTGC | 23092 |
| rs532335531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847414 | CCGGGCTGGAGTGCA[A/G]TGGCGCGATCTCGGC | 23092 |
| rs532336761 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977671 | TCTCTAGAAGTTGCT[A/G]GCCATCTCCTGGTTA | 23092 |
| rs532348918 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846949 | GTCTTATCTCAGAAC[A/T]ACCTTATGAGGTGGG | 23092 |
| rs532353731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173254 | AATATGGAGTGCCCT[C/T]GAACTCTTTGGCCTC | 23092 |
| rs532359998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081619 | TCCTTGTTTATAAAA[C/T]GGGAAGAATAATAGG | 23092 |
| rs532361802 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845466 | CCCTAGATGGAGTCA[C/G]GCCTCTGGGGTAAAG | 23092 |
| rs532362091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984333 | ACATATCAAGGGTCT[A/G]ATTAAGGAAGAAAAG | 23092 |
| rs532368430 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865013 | TTGATTAGTCCCTCT[A/C]AAAATGGGTTTCTTT | 23092 |
| rs532372769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212542 | GGAGCTGGTGAATAC[C/T]AAGGACTCTTCTTTC | 23092 |
| rs532374205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143075752 | CACCCAGGCTGGAGT[A/G]CAGTGGCGTGATCTG | 23092 |
| rs532381466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142943314 | CTATCACAAAATACT[A/G]TAAACTGGGTAGTAT | 23092 |
| rs532387770 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089807 | CCCATGGGACTCTAA[C/T]TGTGTCTAAATAGAC | 23092 |
| rs532396659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933505 | TGGCTTATGTAAGAT[A/G]GATAAGTGTATTTCT | 23092 |
| rs532410371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853565 | TATCACTTACTGGCA[A/C]TTTTCCCTTTTGTAA | 23092 |
| rs532416742 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204069 | CTTAAAGTATAATTA[-/A]AAAAAAAAAAAATCA | 23092 |
| rs532433533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851529 | ATTATGAACAGCTTG[A/G]CATTTTGCCCCTCAT | 23092 |
| rs532433826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135428 | GAGGTACAGTAAAGG[A/G]ACAGAGGCAGGACAG | 23092 |
| rs532438278 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045758 | ATCCCAGCCCTTTGG[A/G]AGGCCGAGGCAGGTG | 23092 |
| rs532441470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948117 | ACGCGGGCTTTGATG[C/T]GGCACTTTAGACGTG | 23092 |
| rs532444956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165900 | ACAGTAGTAGTATCT[A/G]CCTCCTAGGGTTGTT | 23092 |
| rs532454591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087667 | TTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTTG | 23092 |
| rs532456828 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071765 | AAAAATTAGCCAGGC[A/G]TGGTGGCATGCGCCT | 23092 |
| rs532475939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947320 | TTCATTTGGAGGGAG[A/G]GAGGGATGGTGGTGC | 23092 |
| rs532477815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955918 | TACTCCCTCAGAATG[C/T]CAGAATCTTGGCTGC | 23092 |
| rs532482372 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017508 | ACAGGTTTCTTGATT[C/G]ATTCATTCTTTCGTT | 23092 |
| rs532489490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120705 | GGATTCAGATGTTCA[A/G]AGGTTAGTAATTTGG | 23092 |
| rs532497358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990540 | GGAGAAGAGATGCTC[G/T]GATTTTTAGAATTTT | 23092 |
| rs532498074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990866 | TATCAGTTGTCAGTC[A/G]GCCCCTACTGAGTGG | 23092 |
| rs532506305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037410 | ACAAGTCTTGTTGGT[C/T]TCAAGCAGGAGGTCC | 23092 |
| rs532517214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165332 | GAGATGAGGGTGTTG[A/T]CAGTGAGGGAGGAAC | 23092 |
| rs532517750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030396 | CTTGATGGACAAAAT[A/G]CAGGAGGTCTAAAAG | 23092 |
| rs532521905 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127618 | AAATCCTAAGCAACC[A/T]CGCATTCCCAATAAA | 23092 |
| rs532528618 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018891 | TTTTTCTTTGCGAGT[A/G]CATTGAATCATACAG | 23092 |
| rs532529686 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009363 | ATCATGTGGTTAGTG[A/G]TTAAGTGCTTGGGCT | 23092 |
| rs532543161 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138669 | AAGGTGATTTAGCCA[A/T]ACTGAACCTGGAAGA | 23092 |
| rs532543258 | in-del | -/TCTTGTT | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846783 | GCAGATGTCCTTTAG[-/TCTTGTT]TCTTGTTTTCTCTTT | 23092 |
| rs532554075 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022825 | TGCCTCATTGCCAGG[G/T]TCATTTTTTTCCTGC | 23092 |
| rs532556055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031016 | TAACCTAGGTGGGAA[C/T]GTCTGAGTGAGTTTC | 23092 |
| rs532576652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804751 | CCTGCCTTGGCTTCC[C/T]GAAGTTCTGGGATTA | 23092 |
| rs532581123 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010455 | AGTGCTAGGTAAACA[A/G]AACCATTCCTGCTTA | 23092 |
| rs532582874 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974129 | CTGCTTGCTTCTGCT[A/G]TAGTTTAGTGTGCAT | 23092 |
| rs532585830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193943 | TTGGAACATAACCAC[C/G]GAGGATAAGGGGGCA | 23092 |
| rs532597921 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812442 | CCTTGGGTTCAAGCA[A/G]TTCTCGTGCCTCAGC | 23092 |
| rs532603210 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224668 | TCAAATTTTGTGTGC[A/G]TCTGTAAGTTCTTAA | 23092 |
| rs532615484 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181669 | ATGAGTAAACAAATG[-/A]AATTACACCGGAATA | 23092 |
| rs532619118 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998095 | TTAGTGTTTGCTAAC[C/T]CAGTGTTTGTTGCTG | 23092 |
| rs532629703 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073544 | TATTTCCCTATTGGC[G/T]GTAGGGGAGAGCATT | 23092 |
| rs532632476 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768547 | ATGAGAGACCTCAAG[C/G]CTTTGGCTTCCCTAA | 23092 |
| rs532634299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217321 | GTGCAGTGGGAAATG[C/G]ATGTGCAATACGTGC | 23092 |
| rs532640714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804376 | CCAGGGATGCTTCTG[A/G]GAAGCTAGTTTTCAT | 23092 |
| rs532648274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211408 | GGGCAACAGGAATGG[C/T]CCCCTTTAAAAGCAC | 23092 |
| rs532649123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133309 | TTTTTTGTTTTCTTC[C/T]TGAGACTTTTCTGCA | 23092 |
| rs532650161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977723 | AGGGAGAGGAAGCAA[A/C]AACATTTCACACTGC | 23092 |
| rs532651358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159506 | TAAAGGGGGAAAAAA[C/T]GGTGCAGGACAGTGT | 23092 |
| rs532671437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906112 | ATGATTAGATTTGGA[C/T]TATGCATCTCTGGTC | 23092 |
| rs532674097 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888667 | AACTACAGGGCAGTG[A/G]TGTGGAATGGCACTG | 23092 |
| rs532679996 | in-del | -/T | 0.0736069 | 0.177159 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805107 | TTTTCCTTTCTTTTC[-/T]TTTTTTTTTTTTTGA | 23092 |
| rs532688954 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917211 | TGCCCAGCTAATTTT[A/G]TATTTTTAGTAGAGA | 23092 |
| rs532694079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846083 | ATGTGTGAAAGCCAC[A/G]CATTAGTTTCAAGGG | 23092 |
| rs532697618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884483 | TAACTGTTACCCCAT[G/T]ACCATAACTCAGGTA | 23092 |
| rs532721646 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160213 | TACAGGTGCCCGCCA[A/C]CACACCTTGCTAATT | 23092 |
| rs532721977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837984 | TGAGGGTAGGCTGGG[C/T]GCAGTGGCTCATGCC | 23092 |
| rs532723594 | in-del | -/GTTTGTTT | 0.0292639 | 0.117369 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163433 | TAGAAGGAGTTCTAG[-/GTTTGTTT]GTTTGTTTGTTTGTT | 23092 |
| rs532735465 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002870 | GCATAACATTGCAGC[A/G]TTTCCTCCTCTTGTT | 23092 |
| rs532745194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169540 | AAAAGAAAGAGAGAG[C/G]CTCTTTTTCTCAGCA | 23092 |
| rs532754910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842495 | AGTTTATTCTTAGGT[G/T]CAGCACCCAGCACAA | 23092 |
| rs532755173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838429 | GAAGTTAATTTTATA[A/G]TGAGATGGCCAAAGG | 23092 |
| rs532756680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078016 | CCTCTCCTATATTCT[A/G]CCACCATTGAAATGA | 23092 |
| rs532771376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162315 | CACACACACACACGC[A/G]ATCCCCTTTCCCATT | 23092 |
| rs532775990 | in-del | -/CCTTTC | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950946 | GAAGTGAGAATAAGA[-/CCTTTC]CCTTTCCCTTTCCCT | 23092 |
| rs532777404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927376 | TCTGTTGCCATAGAT[A/G]AGTTTTGCAAGTATT | 23092 |
| rs532778022 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920532 | ATCAATAAAGTCTCT[C/T]GAGGGGCAGTGTTTA | 23092 |
| rs532781445 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147825 | CTTCCATAAGGAAGA[G/T]CCCCCAGGAGCCCTT | 23092 |
| rs532783668 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080921 | GACTAGGGTAGTAGT[A/G]GTGGAAATGCTGAAC | 23092 |
| rs532793696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027496 | GCTGACTTTTTAAAT[A/G]TATACATATACTACT | 23092 |
| rs532800599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153937 | GATAAACAAGGCCTG[C/T]GTCCAGACAGAGTTG | 23092 |
| rs532817077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926831 | TTACCCCATACTTAC[C/T]ATCCTGTTCCTGCTC | 23092 |
| rs532818174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944927 | GTTTTCTAGCAGCGC[C/T]GCCCCCTCCCCAACC | 23092 |
| rs532827342 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991446 | CCTGCTTAGGCTCAC[A/G]CTCCATGGGCTGCAC | 23092 |
| rs532832805 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884984 | TGGCTGCCTTCTGGC[C/G]TTGAATATCCTTGTG | 23092 |
| rs532838586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848588 | GGCTGTGTGAACATC[A/T]TAGTTGTGTAGGTGG | 23092 |
| rs532844986 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867240 | CGTGTGTCACGGAAA[A/C/T]GAGAAAAATGCTATG | 23092 |
| rs532850541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855507 | TTCCATCTGCCCATC[A/C]TTATTGACTGCCTGT | 23092 |
| rs532851388 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216132 | TAAGCATAAAGGGGG[A/G]AAAAGGAAGAGAAGC | 23092 |
| rs532859438 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180050 | GACATCTCTCTGTCT[C/G]AAAGGAGCCTCCTTT | 23092 |
| rs532860958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040682 | GCATTAGATTGAAGC[A/G]GTTGCATTTAAGCTG | 23092 |
| rs532869053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814042 | AAGTTGGCTGTTCCT[C/T]AGGAGGGTTGGCCAG | 23092 |
| rs532877976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808229 | AACAGAGTGAGACAT[A/T]GTCTCGGAAAAAAAA | 23092 |
| rs532893118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797447 | CAAAGGTGACTGACT[C/T]AAGGATTTGTCAGGA | 23092 |
| rs532894146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208719 | CAACTTTGAGTTTCC[A/G]TGCAGCTCCCAGCCC | 23092 |
| rs532897507 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023470 | TCTAAAGCCTTCAGC[C/T]ATTACCAAAAATCCA | 23092 |
| rs532921440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189819 | GCCTACTGAACTTGA[A/G]TGTAAGCTGCCTGAG | 23092 |
| rs532936491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828313 | TCCTGCACTCTGTAC[A/G]ATTCCACTTTTACCC | 23092 |
| rs532963011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098197 | TGCTTGACATATTTG[A/T]CCATAAGTTCTAATG | 23092 |
| rs532972090 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077436 | AAAACCCCAGCACCG[G/T]TTCTTCTCATTGTCC | 23092 |
| rs532986122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163006 | CCTGTGGTCCCATCT[A/G]CTTGGGAGGCTGAGG | 23092 |
| rs533005321 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967520 | GGTGCGGTGGCTCAC[G/T]CCTGTAATCCCAGCA | 23092 |
| rs533006130 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875466 | TTATTTCACTTTTTT[C/G]GGCGTCGGATTCTCT | 23092 |
| rs533022678 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070371 | AAACATGTAGATTAT[C/T]CCTTCTTTGTTATGT | 23092 |
| rs533022934 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130283 | TTACCCAGAGTTATA[G/T]TTTTGTTTTACAATT | 23092 |
| rs533026339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064100 | ATCTTTAAAGGGGGC[G/T]ATTTTACTTGAAAAA | 23092 |
| rs533031592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132775 | AGACCCATAGTGCCT[A/G]CTATAAAAGAGATGC | 23092 |
| rs533034235 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047366 | TGGCTCCTGCCTCCA[C/T]AGTAATGTGAGGATG | 23092 |
| rs533038417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930960 | GCTCAGGGTGTTGCT[C/T]AGCCTGTGTGGTTTT | 23092 |
| rs533039086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974438 | GTTGGAAAATTACAG[A/G]CAATGGCCCTCTTTA | 23092 |
| rs533051125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807716 | TAAGCCTGAGGACAG[C/G]ATGTGAGTGCCTGCC | 23092 |
| rs533054655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221669 | CTGGGACTACAGACA[C/T]GCTCCATCAAACCTA | 23092 |
| rs533070559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882256 | GGGGGTAATAATAAA[A/G]CTTGCCTCGTAGAGT | 23092 |
| rs533071280 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160415 | AATAGCTAGGAGTCT[A/C]AATGAGATGCTATTT | 23092 |
| rs533083880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842992 | CGTGATTCAAAGGTC[A/C]CCCAAACCTTTGTTC | 23092 |
| rs533088763 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108281 | TAGACATGTAAACAT[A/G]TGGAATGTGGATGTA | 23092 |
| rs533092092 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992879 | ACCTTCTTGGGGTGA[A/G]CACAACTGTAAGTGA | 23092 |
| rs533096590 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977298 | AACCCGCGGTTCTTC[C/T]TTGAGATTATGGTTC | 23092 |
| rs533100058 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894979 | GCCTGACTTTAGTTT[A/C]GGCCACACCAGCATG | 23092 |
| rs533114142 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871271 | CAATGGGTGCCCCTG[C/T]GCAGAAGCCTCACAA | 23092 |
| rs533114228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105165 | CGGATCACCTGAGGT[C/G]GGGAGTTTGAGACCA | 23092 |
| rs533125402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833548 | TTTTTGTATGTACTT[C/T]TTTCCCCCATTTAAT | 23092 |
| rs533132522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007897 | CTTTCCTTTCCCTTC[A/G]TCTCTTAATTAGTTT | 23092 |
| rs533141481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013837 | CTTGCTTTCTTAAAA[A/G]GAGGGAATTTTTTTT | 23092 |
| rs533141862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915025 | TTGGAAACAAGCCCA[A/G]ATTTGCTTTCTGAAG | 23092 |
| rs533148139 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893606 | TCCTTTTCTTTGGAT[A/T]AATACCAAGTAGTGG | 23092 |
| rs533148209 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916881 | TGTTGTGTCATCCTC[A/G]CTACAACCCAGGGGG | 23092 |
| rs533148715 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785787 | ATTGTTCTAGGAAAT[G/T]CCAGTCCAAATGTAG | 23092 |
| rs533159476 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006161 | AGGAAGGCCTGAATT[A/G]TCTGTTTCCACTCCC | 23092 |
| rs533163961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780112 | AAATACACATACACA[C/T]TGTGCCATATGTGCT | 23092 |
| rs533167909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827864 | TCAATAAACGTCAGC[C/T]GTTACTAGCTAATGA | 23092 |
| rs533179863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922164 | ATTTATGGCCTCAAG[A/G]AGAAACTGTATTAAT | 23092 |
| rs533184117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149404 | CAGCGTCTGCCATGG[A/C]CCTGAGTGAGAGCCA | 23092 |
| rs533185507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924214 | TTGCTTCCTCCCTCC[C/G]TCCTCTTTCCAACTC | 23092 |
| rs533188244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145021 | GGCCCAGCAAGGGAT[A/G]CCAATAAAGAGTCAG | 23092 |
| rs533192364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151323 | ACTCATTACTGGTGG[A/G]AATACAAAGTGATAC | 23092 |
| rs533192609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011742 | ATATAGATGATAAAG[A/T]TGCTGCTGAGGGAGA | 23092 |
| rs533196836 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792894 | TTTCCTTGTTTTCCT[A/G]TCAAACTGTTTTTGA | 23092 |
| rs533201711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055730 | AAAATGCTGTTGTTG[A/G]TAGATGAGTCACTGA | 23092 |
| rs533202023 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820097 | CAATTTCCTTCCCCA[A/G]AGATTTTGATGTAGC | 23092 |
| rs533203278 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807754 | TCATGGGTATCAGCG[A/G]GACAGAGATTTGTGC | 23092 |
| rs533207537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154736 | CTGTTCCTGAAAGAT[G/T]TGGAAACCTCTGAAT | 23092 |
| rs533223364 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923792 | ATTTTAGGAACATTC[C/G]TCTAAAAATACTAAG | 23092 |
| rs533229641 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131987 | GTAAACTTGTTTTTT[G/T]GGGTTCCAGCTGCTC | 23092 |
| rs533232771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143068224 | CTCCTGGGTCAATCA[C/T]GTAATGGAAAGTAGA | 23092 |
| rs533237281 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123128 | CCTGTCCACCAGTGT[A/T]CATTCCCTTGTGTAG | 23092 |
| rs533239820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203615 | CTACTATAAAGACAC[A/T]TGCACACGTATGTTT | 23092 |
| rs533240447 | snp | A/G | | | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058776 | GAAAAAGAGTGATAT[A/G]TATCATGAAGATTTC | 23092 |
| rs533253243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118178 | GAAGAACATTTCAGG[C/T]AGAGGAATGATATGG | 23092 |
| rs533256359 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161838 | AGCAGTGAGATAGAA[A/G]TCATTCTGGGTTTCG | 23092 |
| rs533259433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217820 | CTTCCACTCTTGCTC[C/T]CAGAACCCCTTCTTC | 23092 |
| rs533261748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794985 | GCTTTTTCTGTAAAG[C/G]GCCAGTTAGTAAATT | 23092 |
| rs533262835 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037031 | AGCTCTCAATCAATG[C/T]CAGCTATTATTATTA | 23092 |
| rs533264403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800456 | CTTACTGCAACCTCC[A/G]GGTTCAAACAATTCT | 23092 |
| rs533264525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787003 | TGACTAAGACATTCT[C/G]GTTCTAGAGAACTCT | 23092 |
| rs533270911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889018 | ATTGCAGGGGGCCCA[A/G]GGATGTGATGGATTC | 23092 |
| rs533283126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150718 | AACAACTGGACATCC[A/G]TATACACAAAAATGA | 23092 |
| rs533283415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111765 | TGTAATAATTATTAG[A/G]CCTCGTAAATATTTT | 23092 |
| rs533286629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792130 | ACATTGTTTGCTGAC[A/G]GCGTTTCTGTGTTGG | 23092 |
| rs533290940 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003627 | TATAGACTGTAGGAG[C/G]AGTAAGAGATCAAAG | 23092 |
| rs533292667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018236 | TTCCTACTGATTCTA[C/G]ATACTAATCCCTTGT | 23092 |
| rs533294261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109811 | AGTTGAGACCTTTCC[A/G]AGTCTACAGAGAGGA | 23092 |
| rs533307690 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020676 | TGGAGTCTTGCTCTG[C/T]TGCCCAGGCTGGAGT | 23092 |
| rs533317041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813622 | TTCTTCCCAGGTCTC[C/T]CTTTTTGGCTTGTCT | 23092 |
| rs533325364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983309 | CCTCCCGGGTTCAAG[C/T]GACCCTCCTGCCTCA | 23092 |
| rs533326221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195389 | GTTTTCAGCAGTGGA[C/G]ATTTAGATTCTTATT | 23092 |
| rs533341356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944275 | GTAATAGATTATTAG[A/G]CCTTTAGTCTTTTAC | 23092 |
| rs533354576 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053177 | CAGCAAATATCTGTT[C/T]GTGAGTCCTGGAGAG | 23092 |
| rs533364981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103327 | GTGGAGAAATAGGAA[C/T]GATTTTACACTGTTG | 23092 |
| rs533370157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143006870 | GATCTAGAAAAATCA[C/T]GTCCATTCATGGGTG | 23092 |
| rs533374708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785207 | AGTGCCGGGATTCCT[C/T]AGGATTTTTAACTCA | 23092 |
| rs533377884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952352 | ATGCCTCTAACTGGG[A/G]AGGTTTCTCTTCTGG | 23092 |
| rs533378842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012418 | GTCATATTTCTTAAG[C/T]GAAAAATCCCTTTCT | 23092 |
| rs533381711 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115548 | CCACTAGGGGTTCCT[C/G]GGCAGGATACCAAGC | 23092 |
| rs533389450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196019 | ATCTCATCACCCAGG[C/G]AATGCTACTAATATG | 23092 |
| rs533391501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873015 | GTGGGGGAAACTGCA[C/T]TGACTGTGTGGAGGG | 23092 |
| rs533409590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972766 | CTATATATTTGCTAC[A/G]TTGTGTCCTTTGACC | 23092 |
| rs533410429 | in-del | -/CT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832377 | ACAACCGAGAGCAGG[-/CT]CTCTCTCTCTCTCTC | 23092 |
| rs533412559 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061223 | TGTATAATTCTGTTA[G/T]TTTTATCAGGTGGAG | 23092 |
| rs533416707 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113888 | CTTTTTAGCGTAGGT[G/T]GGACTTGCCCTGGTG | 23092 |
| rs533426651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820230 | CAGGAGACCCCAACG[C/T]TGAGAATTCAGTTCT | 23092 |
| rs533436764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143387 | TATGGAAAGTGAAGT[C/T]GCTTAGCTCCCAGAT | 23092 |
| rs533446290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142972074 | GTTATCCCAGCTACT[A/C]GGGAGGCTGGGGCAG | 23092 |
| rs533454175 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818201 | CACAAAGGAGAATGC[A/C]ATGTACCAATTATTG | 23092 |
| rs533459732 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880218 | CAGGGCTCCTTTGCC[C/T]TGTAATAAATCACTA | 23092 |
| rs533466518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143068856 | ACTGAAATGCCTCAT[G/T]ATCAGTATTGCTGAT | 23092 |
| rs533469461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046909 | TAACTGTTTTGTCAT[A/G]TGACATCAAAATGTT | 23092 |
| rs533472338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886796 | ATGGGCACTATCCCA[C/G]AGACACAGATAATCC | 23092 |
| rs533482575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155414 | AGCAAGATCTCACTC[A/G]TCAATCGGGAGCCCA | 23092 |
| rs533491640 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181946 | CTTAACTAACCTCTC[C/T]GACTTCCCCTGACAC | 23092 |
| rs533492284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915423 | GAGTGCAGTAGCATG[A/G]TCTCGGCTCACTGCA | 23092 |
| rs533492325 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835377 | AGTATTCAGGTGGCC[C/G]CATTCATTTAACTCC | 23092 |
| rs533493364 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826505 | TATTGAATTTCAACT[A/G]CGTGCTAGCACGAGG | 23092 |
| rs533494581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116260 | GCTCTGTAAGCCTAA[A/G]TTCCTGTTTAATATT | 23092 |
| rs533504408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815859 | GAGTACAGTGGTACA[A/G]TCATGGCTCACTGCA | 23092 |
| rs533507334 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138085 | CAGTTGTGTGCCCAG[A/G]TCCCTGCCTGCGACT | 23092 |
| rs533521718 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902187 | AAACTAGGGGCAGGC[A/G]TTTCTAGAGTGCTTG | 23092 |
| rs533533961 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137140 | ATGGTCTCACTGTAT[G/T]ATTCTCTAATATATG | 23092 |
| rs533539320 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901237 | AGATGTTTTTACCAT[G/T]CACTAAAGACAAGAC | 23092 |
| rs533541082 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097592 | TTGGGAGGTCGAGGC[A/G]GGTGGATCATGAGGT | 23092 |
| rs533543527 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061563 | CCTTTGTTGCAGGGG[-/C]ATTGGAGAGGCAGAG | 23092 |
| rs533544242 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911614 | GACCATCTTTATAGA[G/T]TTTTGCTGATATGGT | 23092 |
| rs533544917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854997 | GCCTCCACATCATAT[A/G]TGACAGTAAAGTGTT | 23092 |
| rs533563103 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223513 | CCATCTGACTGGTTT[C/T]CCCATGTCCTCCCAT | 23092 |
| rs533567144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178969 | CCGCCTCCCGGGTTC[A/T]AGCGATTCTCCTGCT | 23092 |
| rs533571291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001258 | AGAGGTTTAGCTTAC[A/G]TGGGTATATGAAATT | 23092 |
| rs533572042 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140073 | TGAATCTTGTAGGGA[A/G]CTTGTTAAAAATACA | 23092 |
| rs533572988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998367 | GATAGGAAAGGACCC[A/G]GAAGCAGCCTTTGGA | 23092 |
| rs533577009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929349 | TCCTGTAAGAGAAGG[C/T]CTCAAAGTATGTTAT | 23092 |
| rs533577933 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793833 | CCTCAAGCGATCTGC[C/G]TGCTTCGACCTCTCA | 23092 |
| rs533582485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909127 | ATCCCTTTGAGTTTC[A/G]CCTCCTTCCCATTCT | 23092 |
| rs533591425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091181 | GGCGCTTTCTTGACT[C/T]GGGTGTGATGAGTCC | 23092 |
| rs533593574 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191718 | CCACCCAGTAGCCAG[C/G]AGCAAGAACAATGCC | 23092 |
| rs533594340 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211724 | CACGTGTCCCATCAT[A/G]CCTGGCTAATTTTTT | 23092 |
| rs533614363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142771926 | GGTGCCTTTTCAGTC[C/T]CCCCATTTAAAAATA | 23092 |
| rs533623584 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056566 | GTCTTCCATTTACAG[A/C]TTCTGATCATTCTTC | 23092 |
| rs533627635 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850833 | TATTAGCTGGATAGC[C/G]AATGGATCTGAAAGG | 23092 |
| rs533639229 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105025 | GAGAAAACATGTATC[-/T]TTTTTTCCCCCTAAC | 23092 |
| rs533645198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958918 | TTAAAAAAAAAAAAA[A/C]AGAAAAAAAAAAAGA | 23092 |
| rs533648493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049593 | GCCAACAAATATTTT[A/G]TAGGATTTTTTATCT | 23092 |
| rs533658929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146537 | CAGTATTCTCCAAGC[A/G]TGAATATGACTGCTG | 23092 |
| rs533660514 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143139220 | CAATAAAAATAAAAA[G/T]AATTATAGCTCTACT | 23092 |
| rs533665059 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175911 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCA | 23092 |
| rs533674445 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226011 | CTTTAGGGCAGATGA[A/G]GAGAATGAATTGGTT | 23092 |
| rs533679573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982552 | CCTGTGGAATTGGCT[A/G]AATAGCGGAAGGAAG | 23092 |
| rs533683011 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873674 | GCTACTCTGGTCTTC[C/T]CGAGTTTTGGGATTG | 23092 |
| rs533683215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867218 | ACCTAGTGGCCACAG[A/G]TAAGACCGTGTGTCA | 23092 |
| rs533683555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821897 | ATTGAGTCAGATCTA[C/G]ATAAAGGAATTTTTG | 23092 |
| rs533697603 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030627 | AGAAAGTGGAGGACC[A/G]AAAGGTTAAAAGAAC | 23092 |
| rs533701785 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933634 | AGCCAGAAAATGAGG[A/T]TGAAAGCATTTCGAA | 23092 |
| rs533703638 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902445 | GGGACACATGCTGGC[C/T]TCCAGCTCAAAGGAT | 23092 |
| rs533706803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097164 | GCCGACATGGCGAAA[C/G]CCCGTCTCTACTAAA | 23092 |
| rs533708113 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957224 | AAGAATGATAATCTT[C/T]TTGATAGTGCTGTAA | 23092 |
| rs533710693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030028 | GTGCTGTTTTTATAG[A/C]CTATATATATGTGTC | 23092 |
| rs533712364 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227937 | TTACAGAGTGAAAAC[A/G]TCTCTCAAGGTGGAA | 23092 |
| rs533716586 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188981 | CAAAATGGAACAAGC[A/G]ACATACTCTTTTAAG | 23092 |
| rs533728593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796362 | TTAGGACCGTAGTTC[C/T]CTTATCTTTAAAATA | 23092 |
| rs533733816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178409 | GGAGCATTGTGTTCA[C/T]TGTATGAGGGTGACA | 23092 |
| rs533736667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932761 | TCCAAAGGGAGGAAA[C/T]GTGTGCAAGGAAGAA | 23092 |
| rs533737451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164579 | ACCCTTCTACTAGCA[G/T]CTCTTCTTCCGCCTC | 23092 |
| rs533739411 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931583 | AGCAGTTTAGAAGCA[A/G]TGGACTAGATATTAG | 23092 |
| rs533741969 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164375 | CTTTTCTGTTTCTTT[C/G]TCTATAAGGAAATTC | 23092 |
| rs533744880 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870375 | GGTTTTTAGGTAGAG[A/G]GTTCTCTTTTTAGTG | 23092 |
| rs533746810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994208 | AGCTTCATAGAGGAG[C/T]ACGTATAGGTAGGGC | 23092 |
| rs533754400 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222663 | AAAGAAGTCAATCAG[C/G]AGAGGAGAGCATTTG | 23092 |
| rs533757985 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092585 | AAATGATAACCATGC[-/T]TTTCCAAAGTGAACT | 23092 |
| rs533762032 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942318 | ATAATGCTTTTACAT[A/G]TATAAAATAAAATAC | 23092 |
| rs533762480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001891 | GGCATCAAGATTATT[G/T]TTGGATTTGGGGTAG | 23092 |
| rs533762589 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984375 | TGTACAGTCCATTAG[A/C]AGTAGCTGTCACACT | 23092 |
| rs533766247 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044215 | AAGCATCTATTTGCT[C/G]ATATAACTGGTAAAT | 23092 |
| rs533769611 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072390 | AACATGATCCAGCAG[C/T]CCCACTACTGGAAAC | 23092 |
| rs533783522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844219 | CCACACCTGGCTGAT[C/T]TTTGTATTTTTAGTA | 23092 |
| rs533788296 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007176 | CTCCAGCCTGGTTGA[C/T]AGCAAGACTCTGTCT | 23092 |
| rs533801190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142947456 | TGCAAGGCATTTTGG[A/G]TGGATACCAATACCC | 23092 |
| rs533816671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824062 | TCATGCACATTTGGG[C/G]ACCAGCTCCACAATG | 23092 |
| rs533819102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810846 | TAAGCGTTGATATGT[A/G]AACTCTAGTGTTTGT | 23092 |
| rs533819915 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144976 | TTTTATAGTCAGGGA[A/G]TGCCAGGTTTCTGGG | 23092 |
| rs533828226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803932 | GTATTTACACAACAC[G/T]TCCTTTGTGACTTTG | 23092 |
| rs533829671 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050162 | CAGCTGGATTTTCCT[C/G]AGGCCTTCATCTAAG | 23092 |
| rs533830443 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143248 | GGCCTGCCAAGACGT[A/G]TGAATTTGGCTTGGC | 23092 |
| rs533836735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132810 | AAGGTGTGTGTTGAT[A/T]GAATGAATGAGCATC | 23092 |
| rs533849880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191278 | ATTATTCTGTAGGTA[C/G]TGTAGACAAATGATA | 23092 |
| rs533860858 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036367 | TTTCCAGCCTTGTGT[G/T]GTTCTCTGCTGTGGA | 23092 |
| rs533860940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172181 | CTGACAAATTCTGTA[C/T]ATGCATGCGTGTGTT | 23092 |
| rs533866586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870110 | GCTTGGCTCCTTGCT[A/G]TGTCTTGCACTGCCT | 23092 |
| rs533886410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888727 | TAGTTTTTGAATGGT[A/G]AAAAAGCTCGCCTCA | 23092 |
| rs533890638 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897760 | GGGTAAGTACTGTTT[G/T]TATCCCAATTTTCAG | 23092 |
| rs533897263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142968419 | TTATATTAGGATCTC[C/T]GGATTGTTTTTGTAT | 23092 |
| rs533897680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125151 | TCAGTTTCTTTAACC[G/T]GGTAAAACACCTCTT | 23092 |
| rs533898531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034745 | TATATGAAGTATATA[C/T]CAAGAAAGCTGTTAT | 23092 |
| rs533911243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961151 | CTTCCATGTCTAGAT[C/G]AGAGCCAGGCACACA | 23092 |
| rs533920620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085643 | TCTATTCATGCTGTC[C/T]CTGTCCCAGACTTTG | 23092 |
| rs533922066 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009336 | CATCATCGTCATCAC[A/G]ATGACTTATTGATCA | 23092 |
| rs533922561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099113 | TCTTTTCTGCTGGAC[A/G]GAAGTTATTTGCATC | 23092 |
| rs533922737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772074 | TTCAGCTAAGAAATC[C/T]TGCCTTAGCAGAGTA | 23092 |
| rs533945910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895978 | CTCCATATATGAATA[C/T]TAAAACCTTAGACCT | 23092 |
| rs533952766 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127152 | CAAGAAAACAAACTG[A/C]TTGCTTTTCATAGTT | 23092 |
| rs533966802 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060740 | GGGCTCTGTGGGTCT[A/T]CTCAGTCAGGCTCGC | 23092 |
| rs533979635 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990268 | TGAAGCTTGTGATTG[C/T]GTCATGTAGTTCTTG | 23092 |
| rs533985599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849568 | TTGTCCTGTGGATCT[C/T]CTCAAGGTTCCCTTC | 23092 |
| rs533989505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855808 | CTAATGACTGACTTA[C/T]ATACTCTCACTTGTA | 23092 |
| rs534002522 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158261 | AAAAACATTGATATA[A/T]TTTTAAAAAGGAATT | 23092 |
| rs534005410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133897 | CCAAGCTTTCCGTTG[C/T]ACTGCTTCAGGCCTG | 23092 |
| rs534007204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211524 | GTTGCCTATCAACTT[C/G]AGAAAAAAACAAGGC | 23092 |
| rs534017997 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205426 | AACACTGGAGGCAGG[A/G]TTGGGGATTTTGTTG | 23092 |
| rs534022660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138216 | TTCTCAGAATGAGGA[C/G]CTTGATGGTTTCTCA | 23092 |
| rs534029671 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117210 | CAGACAGCTCAATTT[A/G]ACAAAAGAGCAGGTT | 23092 |
| rs534034770 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993444 | AAAGTGCTGGGATTG[A/C]AGGTGTGAGCCACCA | 23092 |
| rs534039505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851666 | GGTTATAATCCTTTA[A/G]GCCCTATGTGGCCGC | 23092 |
| rs534044779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215832 | GCGATGGTATGGATA[C/T]AGCACATTTTATGTA | 23092 |
| rs534047366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857543 | CCTCGTCCCTCCTGC[A/C]GCAAGGGAAGCATGT | 23092 |
| rs534067397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890084 | GAGGTTGCGGTGAGC[C/T]GAATTCGCGCCATTG | 23092 |
| rs534069930 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177522 | ATGTATTTGATATGC[A/G]TGCTCACCCATAGCT | 23092 |
| rs534072628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993230 | TGCGGACTGCAGTGG[C/T]GCAATCTCGGCTCAC | 23092 |
| rs534085368 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772219 | TGGAATGCCAGGGCA[A/G]CCCAAAGTGCCAATC | 23092 |
| rs534089848 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065546 | CTCTTATGTAACCTT[G/T]CATGTGAATTATTTC | 23092 |
| rs534096937 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021718 | TCAGCACATTAGTAT[C/G]TGCACATTAGTTGGT | 23092 |
| rs534097476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955331 | TTTTAAAGCCCCACA[A/G]AACAAAACAAAGAAG | 23092 |
| rs534101877 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797496 | GATTCTGCTTAGGAG[A/G]TAAGTGATGCTTTTG | 23092 |
| rs534103158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991386 | CTTGGCCAGGAAAGG[A/G]AATTCCCTGTCCCCT | 23092 |
| rs534105251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917319 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCT | 23092 |
| rs534116770 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140860 | TTAATTCATCCTAGA[C/T]CCTCTCCCAGACAGG | 23092 |
| rs534120503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905763 | GTAATAGCTAAAATC[A/G]CAATTGAACTCTTGC | 23092 |
| rs534122388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994835 | TATGCTCTCCATTTT[A/G]TAGATGGGGTAATGA | 23092 |
| rs534124009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989721 | CACTTATGAAGCTTA[A/G]TTTGGCTGGATATGA | 23092 |
| rs534134276 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958674 | CCTGTCTTGAAAAAC[A/G]AAACAGTATAAGTAG | 23092 |
| rs534142566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924685 | TAATTCTTTCCATGC[A/T]CAAAGGTCTTGCAGA | 23092 |
| rs534165832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151847 | CCTGTAGTCCCAGGC[A/T]CAGGAGGCTGAGGCA | 23092 |
| rs534172495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170052 | GTTGATTCATTTAAA[A/C]AACAAATTTCTGGGA | 23092 |
| rs534179160 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787460 | TCTGAGTCTTTGCAG[A/G]TGCTCGATCTAGAAT | 23092 |
| rs534184668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163372 | TAGATCTGCCTTGAA[A/G]TGTATAATTTCCTCA | 23092 |
| rs534215719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937963 | TGTTTTGATCTTGGT[G/T]GTTAGTTATATGAAA | 23092 |
| rs534229307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204639 | CCAGATAATTTCAGC[C/T]GTGTAGTTCTGGCCA | 23092 |
| rs534235760 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142857402 | TGGGGGAGGGTGGGC[C/T]AGCAGCTGCTAGGAT | 23092 |
| rs534256704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119191 | GTTACTTTAGTCAGA[C/T]GTAGTGTGGAGAAGC | 23092 |
| rs534260149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982215 | AACCCAGCAAGTTAC[A/G]TAAGTTGTTGGAGCA | 23092 |
| rs534262733 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044554 | GATGGCCTGGATCCT[A/G]TGCGTATGTTGGGGG | 23092 |
| rs534263054 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057369 | GGAGCAGCTCTGGGT[A/G]TGCAGTTGACTGGCT | 23092 |
| rs534264782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794797 | AGTTCTGTAATACCC[C/T]GGCCAATGATTGACT | 23092 |
| rs534282373 | in-del | -/AAAAA/AAAAAAA | 0.425586 | 0.17796 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154160 | TGATTTAAAAATATT[-/AAAAA/AAAAAAA]AAAAAAAAAAAAAGA | 23092 |
| rs534284306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986012 | TTTATAATTCCTTTG[A/G]TATATACCCAGTAAT | 23092 |
| rs534286348 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122116 | CTGATACCAGCCACC[A/G]GAATGAGATTTTTTT | 23092 |
| rs534294357 | snp | A/G | 0.000214332 | 0.0103499 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142885343 | GAAAAGTATTGTGGC[A/G]TCTTAGAAAAACACT | 23092 |
| rs534297028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893165 | GTATTTTTAGTAGAG[A/G]TGGGGTTTCACCATG | 23092 |
| rs534306935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847074 | CTGTTGCTTGCTCTC[C/G]GTGCACCTTGGGCAA | 23092 |
| rs534312741 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041573 | GAAAGCTTCTTTCGC[C/T]GCTGATGACTGAACT | 23092 |
| rs534315383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142927987 | GCTTATTCAAGTATT[C/T]ATTGTATTGGGTGGT | 23092 |
| rs534316451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855346 | TTTTTTTCAGATACT[A/G]GGAGGCTGCTGGTTG | 23092 |
| rs534318048 | in-del | -/GTTTGTTT | 0.112344 | 0.208688 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163440 | GTTCTAGGTTTGTTT[-/GTTTGTTT]GTTTGTTTGTTTGTT | 23092 |
| rs534319542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073907 | TTTTATACAGCAGGA[A/C]TGGGTAGGACAGGAC | 23092 |
| rs534319728 | in-del | -/GAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115367 | AAAAAACGAAAGAAA[-/GAAA]AGACGTACTATTATG | 23092 |
| rs534320253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034198 | TTTGGCAATTCCTCA[A/C]AAAGTTAAGCACGGT | 23092 |
| rs534323285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991620 | ATCTTTATACCATAT[A/T]TTTACTGTACGTTTT | 23092 |
| rs534344825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085098 | CGGGTAGAGTTTCCT[C/T]TCCCTCACCCCATGC | 23092 |
| rs534347170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808004 | ACTTTGGGAGGCCGA[C/G]GCGGGCGGATCACGA | 23092 |
| rs534355742 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147552 | TTTTTAAAGCATCAT[C/G]ATCTCAGAGGGAGTC | 23092 |
| rs534359567 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015321 | AATAATGAAGGAATA[C/T]GTAAGGCTGTATGGT | 23092 |
| rs534368936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219242 | CCTTAATTTTCTCAT[A/C]TGCAAAATACAGATA | 23092 |
| rs534373956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089317 | GTGACACAGCACCCG[A/G]CAAGAATAAGTACAC | 23092 |
| rs534379457 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143082321 | ACTGTCACAAAAATA[G/T]GGAGTTGTGTTTACT | 23092 |
| rs534380666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925191 | TGTGTGCTCTCTGTT[C/G]TGCCGCAGTCCCCAC | 23092 |
| rs534382947 | snp | A/G | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964323 | TGTAACATTTGTTCT[A/G]TTTACTAAATTCTTT | 23092 |
| rs534385915 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901349 | AATATGGAAATATTT[C/T]AATAAAGGAATCCAT | 23092 |
| rs534389616 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143122211 | ATTTGCCCACATAGT[C/G]TCTGTCCTTTTACTG | 23092 |
| rs534405835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835790 | CAATAGTGGTTAGCC[A/G]CCAACACCAAGAGAT | 23092 |
| rs534420666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887793 | AACATGGTGAGACCT[C/T]GTCTCTACTAAAAAT | 23092 |
| rs534426801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213314 | CAAAAAAAATGCCTC[A/G]TGTCCCCTCTCCCTT | 23092 |
| rs534427324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064466 | TCCATGAAAGAAGTG[A/G]GTGATACCGCTTCCT | 23092 |
| rs534429339 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142802554 | TGTTGTTTTACTTAA[A/C]GTTGCAGTTTCCAAG | 23092 |
| rs534430677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142859206 | CAGGAGGGAAGCGGG[A/G]AGGCCAATTAGGAGT | 23092 |
| rs534434388 | snp | A/C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150065 | GTAATGCTAAATCAG[A/C/G]CATCAAAATTAGAGA | 23092 |
| rs534438254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852681 | CCATGATTTGGTCGA[A/G]TGTCTTGGAAGGAGA | 23092 |
| rs534449606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070610 | TTCAGTGCAATCCCT[A/G]TCGAAATACCAAGGA | 23092 |
| rs534462604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966093 | TATAAGGTTGGGATG[A/G]CAGAGAAAAGAATAC | 23092 |
| rs534466073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804916 | TGGGCCATTTCTGGC[C/G]ATCTTGTATGAATGG | 23092 |
| rs534467267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142843376 | GGCTCATTGAAGCAA[A/C]TAATGTAGGGTTCAT | 23092 |
| rs534469240 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790346 | GCATCCCTTTATTAA[A/G]GGAAAGACTCTGCTG | 23092 |
| rs534469253 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835289 | CACATTTGTACCTTA[A/T]CCCATCAGAGATAGA | 23092 |
| rs534478435 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208274 | CCTAAACGTGCTTCT[C/T]TCTCAAGCTTAGTCT | 23092 |
| rs534487488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102401 | TCAGTGTCGGCCCCA[A/C]ACATGCAGAAAAGGG | 23092 |
| rs534492854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974773 | ATACATTTTTGGAAA[G/T]ATTTTTTCCTCCTCA | 23092 |
| rs534495415 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170151 | GCTGGCCTCCATTCA[C/T]TTTAATGACAGTGTT | 23092 |
| rs534503915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148687 | GTCTCTTCCGGTTCT[C/G]CATGGCTGGGCTTGC | 23092 |
| rs534505099 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824352 | ATAGTTCCTGAGGGT[C/T]GTCCCTATCAAACAC | 23092 |
| rs534509796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004633 | CCTTCCTGGGGACTC[C/T]ACCCTGACCTTCATC | 23092 |
| rs534512063 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933487 | AGAGACTCTGAAGTA[C/T]GGTGGCTTATGTAAG | 23092 |
| rs534526121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785003 | GCGATCTCGGCTCAC[C/T]GCAAGCTCCGCCTCC | 23092 |
| rs534536021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011277 | CGAGAGGCATTTCCT[C/T]GCCTAAAGTCCACAA | 23092 |
| rs534544564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112221 | GACCTAGAGTGAGGT[A/G]TCCAGAAAGACCACT | 23092 |
| rs534549512 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881993 | TCTGGAGTAGGGCAC[A/G]ACCCCTGGTGCTTGA | 23092 |
| rs534549610 | in-del | -/GTA | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907459 | TAAGACCCACTGGAT[-/GTA]GCATCAATGGGAAAC | 23092 |
| rs534558738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784407 | AGTGGGGCTTGCTTG[C/G]GATTTTGTGCTTGAA | 23092 |
| rs534582867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838759 | CATGTTGTGGGATCA[A/G]CTTTGGAAAAAGAGA | 23092 |
| rs534589262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935070 | TATGGATTTTATCTA[C/T]GTAGTAAATTTGAAT | 23092 |
| rs534599601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115375 | AAAGAAAGAAAAGAC[A/G]TACTATTATGATTTG | 23092 |
| rs534599865 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166776 | TACCAACCTTTCAGC[A/G]GGAACTGAAGGTAGA | 23092 |
| rs534613295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886221 | GGCTACCGTGGCTTC[C/T]AGGCCGGCCCTTTTT | 23092 |
| rs534624071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879073 | TAACTTAGACCCCAC[A/T]CTTTTACCAGTTCCC | 23092 |
| rs534628214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942731 | TTGATTAGTGGGACT[A/G]TTTGATTAATGTCTG | 23092 |
| rs534644577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109200 | TACGCCCCAGTTCAG[A/G]TTTGGCTAAGATTCT | 23092 |
| rs534661660 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154880 | AAAAGCAATTTTACC[A/G]TCCCCATGCTATTTT | 23092 |
| rs534662683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192969 | GCGCTCCTCATCTAC[A/G]GTTTTGCTTTCCTTG | 23092 |
| rs534669702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941166 | GTAGTTCTGTTTTAA[A/G]TTCTTTGAGGAATCG | 23092 |
| rs534683209 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067724 | GCTATGTACTTGGAG[A/T]TGCCTAGAATTGGGT | 23092 |
| rs534686701 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143152945 | AAATATCACATTGTG[A/G]TTATTGGAACCCAGT | 23092 |
| rs534691575 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065986 | TCTCCGCCTCATTCC[A/C]CCAAGAATCCCCTGG | 23092 |
| rs534707405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838039 | CGAGGCAGGTGGATC[A/G]CCTGAGGTCAGGGGT | 23092 |
| rs534710165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134909 | AGGGCCAATTACTGA[G/T]AGCAGCTACTACCAT | 23092 |
| rs534720253 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100965 | GAGTGTGGTGACGTG[G/T]GCCTGTAATCTCAGC | 23092 |
| rs534733848 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810867 | TAGTGTTTGTGTCCT[A/C]CATAAAGCGATTTGT | 23092 |
| rs534740217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143058299 | GATTTTTGAAGTTAC[A/G]TGCATTAAAGCCTTT | 23092 |
| rs534741651 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174047 | CATCTGTTTCTTCCA[A/G]TAGCCTCTCCATGTT | 23092 |
| rs534742075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142870970 | GACAGGTGTCCACTT[A/T]AGCTGTACTGAAAAA | 23092 |
| rs534772267 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158853 | AGCCTTGTCTTCAGG[A/G]AAAACCAAGATGTTA | 23092 |
| rs534777945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194954 | CTGAAGGAGCAGGGC[C/T]AGGTGTGGAAGATAT | 23092 |
| rs534782325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969486 | TCCTACATTAGAGGC[C/G]AGATTTAAACAAATA | 23092 |
| rs534782388 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180506 | CATTTTGTCACTGCT[A/C]TAAAGAAATACCTGA | 23092 |
| rs534786237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109874 | TTCTAATTGCTTTTC[A/G]TCTCACTCAGTCAAG | 23092 |
| rs534800987 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154764 | AATCCCACAGGGTAC[C/G]TGATAATTGTGTGCA | 23092 |
| rs534801579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205875 | TGGATATTTTAGACA[C/G]TGGATATACAGCAGT | 23092 |
| rs534811955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142825270 | CTTGTTATTGCTACT[A/G]CTGCCATCCTTATTG | 23092 |
| rs534815624 | snp | A/G | | | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192723 | AAGGGAAAAAAATGG[A/G]AGTCATAAGCTGACA | 23092 |
| rs534818522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832479 | AGGACCTGACCTTGC[C/T]GGCACCCTCATCTTG | 23092 |
| rs534835637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921640 | AGCACCCTCATTTCA[A/G]ATATGTTTGTATGGC | 23092 |
| rs534865319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899665 | CTGCCCCCTGAGGAG[C/T]GGACTTTCATTTCCC | 23092 |
| rs534879066 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142769553 | ACACAGCACATAGTA[A/G]GTGCTCAATATCTGT | 23092 |
| rs534886385 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117465 | TTGTGAGCAGTAATA[A/G]TCAAGTGATGGATCA | 23092 |
| rs534887500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839670 | CAAAAAAGTTCTGGA[A/G]TGAGGCTTTCCTGAG | 23092 |
| rs534888304 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849220 | ATTTTCACTAGCTAA[A/G]GCAATTCCAGTAGGT | 23092 |
| rs534891474 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037704 | CCAAGTTGCAGGTAC[C/G/T]GCTAATGCTCCTGTA | 23092 |
| rs534904738 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889008 | TTATAATTCCATTGC[A/G]GGGGGCCCAAGGATG | 23092 |
| rs534908616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906532 | TCTATCCATCCATCC[A/G]TCCGTCCGTTATCCA | 23092 |
| rs534915604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024561 | GACAGAGACTAAAAT[A/G]TTTCCCCCACTGCCA | 23092 |
| rs534915757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879588 | TAGGCAGAAAACTCT[A/G]TAGAGCCCAACTCAT | 23092 |
| rs534916255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865249 | CACAGCGGTCATTGA[G/T]CCAGTAAATGTTTAT | 23092 |
| rs534917958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201660 | TAACCATCCCTGTGC[A/G]TCTTATATCTCACAT | 23092 |
| rs534920823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173534 | AAGAGTCAACATTTC[C/T]GAATTCAGGCACTTC | 23092 |
| rs534921298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194318 | AGTAGGATGGACTGG[A/T]ATGGTAAAAGGTAAA | 23092 |
| rs534923714 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096276 | TCACCACTTATTTTA[A/G]AAAGTCATTAAATAT | 23092 |
| rs534929910 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164615 | GTTTATTCTTTTCAC[C/T]AGTATGCCAACTCCA | 23092 |
| rs534942545 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915420 | CTGGAGTGCAGTAGC[A/C]TGATCTCGGCTCACT | 23092 |
| rs534944563 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886946 | TGGCTGTGCTTCACA[A/G]TGACCAGGTCTGCCC | 23092 |
| rs534944921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949099 | GAAAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 23092 |
| rs534961842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185478 | TCTTTTACCAAAAAC[A/G]AAGTAGAAAGAAAGT | 23092 |
| rs534961866 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193584 | GTAACCCTTACTTTA[C/G]TTAACAGTGGCCCCA | 23092 |
| rs534972209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964341 | TACTAAATTCTTTTC[C/T]TTGATTTGATTCACT | 23092 |
| rs534977720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051091 | AATTCTTAACATGTG[C/T]GTGTATTACTTTCTC | 23092 |
| rs534984834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200023 | CCCTCTTGTCAAAAT[A/G]CCCTTTGGAAAATTA | 23092 |
| rs534992016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:142919866 | ATTAGCCGAGCATGG[G/T]GGTGGGCACCTGTAA | 23092 |
| rs534996006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972543 | AAAATAACTTTTATT[G/T]TGTGTGTTTAAGGCA | 23092 |
| rs535008651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009863 | TGAAGGTGCATTAAC[C/T]GTTTCAGTCTTCTGA | 23092 |
| rs535009248 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202205 | ATGCACTTCTTTGTC[-/T]TTTTTTCATCTTTGT | 23092 |
| rs535010229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963569 | TAATATCTAAACACC[A/G]TACTTACAAAACAAA | 23092 |
| rs535022171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186027 | GAAGTTAAGAGGCCA[C/T]GGCTCAGAAGGAAAA | 23092 |
| rs535026880 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108467 | CTTCTAATCAAATAT[C/T]CAAACATAATCTAAA | 23092 |
| rs535030021 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094634 | GATGGAACAATGGTG[A/T]GCACACACTTGGACA | 23092 |
| rs535033361 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906876 | TTTATGTTTAAACAA[-/T]TTTTTTTTTTTAACA | 23092 |
| rs535033442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782985 | GCAGGTCTGGAAACC[C/T]GAATTTCCTATACCC | 23092 |
| rs535035512 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775262 | TACATTCTGCTCAGC[A/C]CTTGGTTTTGTCTGT | 23092 |
| rs535036559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967141 | AGGTGTTATTCTTAA[C/T]GTTCTTTTAGTGCTG | 23092 |
| rs535037747 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790430 | CTTACTCATTGGAAT[C/T]ATGACCACCTGGAAC | 23092 |
| rs535058070 | snp | A/G | 0.000252408 | 0.0112312 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147390 | ACTCACTGTAAGTAT[A/G]ATGTCCAGCTGCCTA | 23092 |
| rs535070108 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019455 | GTCTTTTTGCTGTTC[C/G]CTACCTTTGGGTACA | 23092 |
| rs535074081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196819 | ACCTCAGCTGGGAAT[A/G]TGCCGTTGGGCGACT | 23092 |
| rs535075220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142789760 | ACTCGAACACTTGGG[C/T]GGTTCTGGGGTAAAC | 23092 |
| rs535079820 | in-del | -/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999542 | TATGACTCAGAAGCA[-/C]CTCTAAATAATGTTT | 23092 |
| rs535099532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884608 | CTCTCTAGTTTTCCA[A/G]TGACTAGTTATGCTT | 23092 |
| rs535105436 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143228511 | TCATGTCGCAAGAAA[A/G]ATCAAACCCATGAAT | 23092 |
| rs535115058 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836502 | CTGTTTGAGGCTTCA[A/T]GTAAGAAGAAGTCTC | 23092 |
| rs535120703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022425 | GGGTCCACTTTTTTT[A/C]GTAAAGGGCCAGATA | 23092 |
| rs535137374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874809 | GGAACTCTGCCCCTT[C/T]CAGCCCGGGGCCTGG | 23092 |
| rs535148741 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143069914 | CTTGGTTCCCCAGAA[A/G]CCTGATTCTGTTTTT | 23092 |
| rs535148825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833941 | GGCCATCTTTAGACT[C/G]ATAAGTGGGACAGTC | 23092 |
| rs535152615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150831 | ACCTCTAGAAGATAA[C/T]ATAGGAGAAAACCTA | 23092 |
| rs535153576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984427 | AACCAGAAGTGTTGA[A/G]TGACTTAGAAACTCC | 23092 |
| rs535166684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966493 | AATGACTTGGGTTAT[G/T]CTCAGCATTGTTTCC | 23092 |
| rs535169829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849930 | AGTCCCCAAACCCCA[C/T]GGGTGTTCTTCTGCA | 23092 |
| rs535177211 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044984 | ATTTCAAAGATGACA[G/T]ATTATTATGTAAGAT | 23092 |
| rs535185973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817825 | TATAGGACCAGCCAT[A/G]CTAATGTTGAAAAGC | 23092 |
| rs535188600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974113 | TTTATTGCTTCATAT[C/G]CTGCTTGCTTCTGCT | 23092 |
| rs535193233 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064990 | TCCACTTATGTTTGG[A/G]TTTATTTTCTCAATA | 23092 |
| rs535204838 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094907 | GGAGTAGGTAATCAA[A/G]AAAGGTTGCTTTAAG | 23092 |
| rs535223080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981157 | GCTGCATGTGGCAGC[A/T]GTATCAGCTGGTTAG | 23092 |
| rs535233278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180465 | TTTCTGTAGTTCCAT[C/T]TATCAGCAACATATC | 23092 |
| rs535234044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913599 | CAGAAATGTGTGTTA[C/T]ATCTCCAGGAGATTG | 23092 |
| rs535234516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020130 | GGAGTCCAGGCTTCC[C/T]GTAGCTCTTCCTTCA | 23092 |
| rs535238102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794061 | CTGAAGACCTGCCAG[A/G]CTCTCGTGACTCCAA | 23092 |
| rs535250149 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136138 | TGTGGTTAGAATGAA[A/G]CAGAAGCAGCTTTGG | 23092 |
| rs535250886 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981636 | AGCAGCAGCTTGGCT[C/G]CTTTCCTGCAGAGCA | 23092 |
| rs535258411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143092385 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 23092 |
| rs535269017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993638 | ACAAACTAGATTGTT[A/G]ATTTTTTTTCTTTTT | 23092 |
| rs535281489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044606 | GTTGGGGTGGGGACG[A/G]GGTTAGTCCCTGAAA | 23092 |
| rs535288442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141107 | ATTCCTGTTGTCACA[C/T]GGGCTGCAGAAGGTG | 23092 |
| rs535303452 | snp | C/T | 0.000236678 | 0.0108758 | synonymous-codon, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222380 | ATCTCAGGAGCCTGG[C/T]TGGTTGGAGGGGACT | 23092 |
| rs535313246 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102865 | CTTTGTCCTTACAGC[A/G]TCCCAGTGCCTCTAT | 23092 |
| rs535323179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775899 | TCTCTTTTAAAGTCA[C/T]AAAAATGTATTTTTT | 23092 |
| rs535324594 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862022 | GTCTGTGACTTTCCG[A/G]ATTCACAACTGTTGA | 23092 |
| rs535329130 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129011 | TGTGACAGATGGGAT[C/T]GAAGAAGGTCTAAAA | 23092 |
| rs535329394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871378 | TGCTGGGAGCTTTCC[C/T]GAGCCTGGCTTGCAT | 23092 |
| rs535335376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051832 | TTCACAACTCCCAGA[C/T]TTGCCAACTGCTGCT | 23092 |
| rs535335975 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095500 | TTAAAACTAAAACAA[G/T]TTTAAAGCTTTATTT | 23092 |
| rs535342148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182594 | TCCTTTACCCAAACC[C/T]TGTCATTAACATGGA | 23092 |
| rs535345300 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143190046 | GGGGGAAAAAAAAAA[A/C]AAGACCTGGTTTCTG | 23092 |
| rs535347140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145199 | TATTGTTTTTAGTTT[A/G]TAGAATGATAATCCT | 23092 |
| rs535372320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783343 | CAGCAGCATTGCCAG[C/T]GGATGTGGGGGAGCT | 23092 |
| rs535378212 | snp | A/G | 1.73782e-05 | 0.00294767 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772786 | CTTGCCCGGAATGGA[A/G]CCTCTTGCACCAAGC | 23092 |
| rs535383937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960244 | GCACCAAATAGTAAT[C/T]ATGAGCCTAAATTGA | 23092 |
| rs535400847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048774 | CAAAAATTAGCCAGG[C/T]GTGGTGGTGCACATC | 23092 |
| rs535401653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104426 | AGAGGCAGGAGAATC[A/G]CTTGAGCCTGGGAGG | 23092 |
| rs535410799 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875881 | GAGTAGCTAGGACTA[C/T]AGGTGTGCACCACTG | 23092 |
| rs535412333 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039539 | TTTAATTTTTTTTTT[A/T]AAATTTAAAAGAAAA | 23092 |
| rs535420461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813094 | AGGTGCCGGCTACCA[C/T]GCCCGGCTAACTTTT | 23092 |
| rs535429852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820804 | GTGTCAGGCACATCA[C/T]GTATGCATTTTCTTA | 23092 |
| rs535434827 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050978 | AGAGCTTTTGGATCT[C/T]AAAACAGAAGGGACT | 23092 |
| rs535435176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175448 | GCATGAGTTTTTCTT[C/T]TGTAAGTATGTAAGA | 23092 |
| rs535440562 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097753 | CATGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 23092 |
| rs535440572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142827159 | TTTCTAATGAAAAGC[C/T]GGAAGTTGCTTGGTG | 23092 |
| rs535461171 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998446 | TCCCATCCTCCACTC[G/T]GGGGAGGGGACCCTA | 23092 |
| rs535464333 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868465 | CAAAAGTGGATGTGG[A/G]GAGGCCAGAGAGGAG | 23092 |
| rs535474315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055240 | TCAGAAATAGCATAA[A/G]TCTCTGTGCAGATTT | 23092 |
| rs535480138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812646 | CGCAGCTTCAATCCT[C/T]CCTCTTCTGCCTCCC | 23092 |
| rs535485411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142771166 | CAGCGCGGGTGGTGC[G/T]CTGGGGCAGCGCGGG | 23092 |
| rs535488365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794541 | GGTTTAATAAAGTAA[A/C]CCTGGACATTCAAAT | 23092 |
| rs535488923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144516 | GCTGAAGCAGTTCTC[C/T]TGCCTCAGCCTCCCA | 23092 |
| rs535497331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786296 | CCTAATACATTTTTT[A/T]AAAAGTTAATTTCTT | 23092 |
| rs535503020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842559 | TTCATCCCTGTGTGT[C/T]GGGAAGGACTAGGAG | 23092 |
| rs535505909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819349 | TGGGTGGGCATGTTT[A/C]ATCTCACTGATGGGG | 23092 |
| rs535514003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129220 | TTATATTTACACTTA[C/T]AAATTAAATCCTCAT | 23092 |
| rs535516484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143115 | TACTCTTAGGCACCA[C/T]GGAAAGTTGGGATAT | 23092 |
| rs535524825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203205 | ATCCAGAATCTACAA[A/G]GAACTTAAACAAATT | 23092 |
| rs535525477 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047086 | TGTGATTTTCTCAGG[C/G]ACATATTGCACAGAT | 23092 |
| rs535529710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874155 | AAAGAGGCTGAGGTG[G/T]GTTACTGTTTATCAC | 23092 |
| rs535539591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117448 | AACATAGCTGTACCA[A/G]GTTGTGAGCAGTAAT | 23092 |
| rs535540321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196247 | TTCTCCTCCCCCATC[A/G]CAGTCCTCTTCTTCC | 23092 |
| rs535556185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142881153 | GTGGCCTTGGGGCCT[G/T]TGCCTCCCCACTCTT | 23092 |
| rs535569070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778423 | CAGTTTGGTATGCAT[C/T]TTTTCTTGTCCTTTT | 23092 |
| rs535583626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785261 | TATCTGCTTCGTCTC[G/T]TGATCTTGTGAAGCC | 23092 |
| rs535592203 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108504 | GTGACAGGACATATA[A/G]GTTTGTCAATTCCAG | 23092 |
| rs535592602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177555 | CTTGGAGACAAGGTG[C/T]TGTCGGCAGACCAGA | 23092 |
| rs535593535 | snp | C/T | 1.67253e-05 | 0.00289178 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907673 | ATACAGTGGAATGTA[C/T]AGATATTTTATGGGA | 23092 |
| rs535595329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915070 | TGTTTTCATCTTCAG[A/G]AGTTTCCCGAGAAGT | 23092 |
| rs535599159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815101 | TGCCTCCCGGGTTCA[A/G]GGGATTCCCCTGCCT | 23092 |
| rs535600312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041643 | TAGACAGCTGTACCA[A/G]ATCCCACTCGTTTGC | 23092 |
| rs535606988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826006 | AAGATAGAAGACCTA[A/G]ATTTTCTTATCGATT | 23092 |
| rs535615737 | in-del | -/GGGTGT/GT | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779424 | CCTGGGGTTAGGGTG[-/GGGTGT/GT]GTGTGTGTGTGTGTG | 23092 |
| rs535617380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181668 | GAATGAGTAAACAAA[C/T]GAATTACACCGGAAT | 23092 |
| rs535617785 | snp | A/G | | | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194402 | GAGCAATGGGGAAGC[A/G]TTGAAGTGTTTTAAG | 23092 |
| rs535618545 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873836 | ATGTAGAACACAGGT[-/A]GATGAGGGGAAATTT | 23092 |
| rs535642732 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124284 | AGGTGTGGAAACCTA[A/G]GCATCTAGCCATTGG | 23092 |
| rs535645008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929908 | GAGGGTAACTTTGCT[C/T]TCTAGGGCAGGGGGA | 23092 |
| rs535655023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841857 | GATTTTTGTTTTCAG[A/G]GGGAGGTCCTGTTGC | 23092 |
| rs535660247 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170246 | TGTCTTCTGTGAGAG[A/C]CATGAACATGCAAAA | 23092 |
| rs535662534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821760 | GCCAACTCTGTGTAG[G/T]AGGAATTTTTATTAA | 23092 |
| rs535671644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131448 | AAGCAGGATGAGAGG[A/G]AAAATAATGAGAACC | 23092 |
| rs535678398 | in-del | -/GCACTATGCAGGAAG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791461 | TATCTTTCATAAGTA[-/GCACTATGCAGGAAG]GCCAGGTCTGCTTGG | 23092 |
| rs535680721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936976 | TTTTAGATGCAATGC[A/G]GAAAGCATACACAAC | 23092 |
| rs535686723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ARHGAP26 | GRCh38.p7 | 5:143069361 | AATAAATATTTGTTG[A/C]ATAAGTGAATGAGTG | 23092 |
| rs535694827 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999706 | ACAAAATCTATGCGA[G/T]CTGGGATTGGCAAAA | 23092 |
| rs535699383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869401 | TTTTTTTGTATTTTT[A/G]GTAGAGATGAGGTTT | 23092 |
| rs535699704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007935 | TTATATTACATTGCC[A/G]ACAAGACCAATGCCA | 23092 |
| rs535707584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137593 | ACTTGCCCTGCGATC[A/G]TTTTCAGAACCTCAT | 23092 |
| rs535715437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936182 | GAGTTCAGCAAGGTC[A/G]CAGGATACAAGATAG | 23092 |
| rs535719915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848808 | GCTCCCTCACTATGT[A/G]ACCTAGCCATGGCTT | 23092 |
| rs535726784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953133 | CTTGACAAAATGAAC[A/G]CCCACACCAACCAGG | 23092 |
| rs535730007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807810 | CTTGCCTGTCCTTGG[A/G]AACTGGGGACTTTAC | 23092 |
| rs535731811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040284 | CATGATTTTACAGGT[C/T]CTTTTTAGCTGTAAA | 23092 |
| rs535736097 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229130 | TTTGGTGACAACCAC[C/T]GTGCTTATTTCTGAT | 23092 |
| rs535739801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944432 | GAATGGTATGCATAT[C/T]TAATATTCCAGTAGA | 23092 |
| rs535765553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041220 | ATTTTTTGTTTAGAT[A/G]TTTAATTTAAAAGTA | 23092 |
| rs535769781 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138295 | CTCCTCATATCATAG[G/T]CAATGTGTGATGGAA | 23092 |
| rs535771221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772319 | CTTACCTGAAACATA[C/T]GAACAGACCCTTCCT | 23092 |
| rs535790926 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813672 | GGTCTTTTCTCTGCT[C/G]TGCCTGTGTCCTAAT | 23092 |
| rs535793317 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142807357 | AAGGGGCCAAGCCAG[A/G]GTTCAAACCTAACCT | 23092 |
| rs535793664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181970 | CTGACACGGCTGCCT[C/T]CCTGGCTTGTACGCT | 23092 |
| rs535800498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901573 | TTCTGAGGAAATGAT[A/G]TTCTCAGCAGGTGGT | 23092 |
| rs535807555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810927 | TTGGGAAGTTCTGTT[G/T]TAGATTGTACCAGCT | 23092 |
| rs535813447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906244 | TTGTCTGGTTTCTCC[A/G]CTATACAGTCACTAT | 23092 |
| rs535816558 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227476 | GTTTGGCAGCCACAC[C/T]GATCGGCTGGGTGCT | 23092 |
| rs535817303 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899987 | AGGATAAATCATAGT[G/T]AATAGGAGGAATGAC | 23092 |
| rs535817677 | in-del | -/ACA | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912253 | AAGCCCTTGATATGC[-/ACA]ACAATGTGGATGAAT | 23092 |
| rs535825722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992333 | ATGATTTTTATTATC[G/T]TAACACTATTGAATA | 23092 |
| rs535836188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143090095 | AGGAACACTAAGTTT[C/T]CTCCCTGTCGTGAAC | 23092 |
| rs535858402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176172 | ACAATGAAACAGAAT[C/T]GTCTTTATGAGATTT | 23092 |
| rs535859856 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934670 | GTCGGTGTTAGTGTC[A/G]TTGCCTTATTTCAGG | 23092 |
| rs535875074 | snp | A/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798345 | GCCCTCTGATGCAGC[A/G/T]TTCCTCCGCTTCCCT | 23092 |
| rs535878798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133456 | TGCAGCTGAGGACAA[C/T]TGATGAGGATTGGGA | 23092 |
| rs535880823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772377 | TTAGGGGATGGGGGT[C/T]CCTGGTTTGGAGTAA | 23092 |
| rs535881916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220735 | ATCTGAAATTGGCCA[A/T]CTTTGGAGGCCAACT | 23092 |
| rs535885408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142994927 | AACAAACAATGGGGG[A/G]AGGATTCCCTATTTA | 23092 |
| rs535887464 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143173025 | CTGTTGGGAAGGTAG[A/T]ATTCCGTGTACGTGA | 23092 |
| rs535901275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140166 | TATATTTTTAAAGCA[C/T]CCTAGTGATACTGAT | 23092 |
| rs535909631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860009 | ACACTTACCTTGCAC[G/T]TACTTTGAGTCTCAC | 23092 |
| rs535918094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002016 | GTTGGATAACATAAC[A/G]TTCACCTTCTGCCTC | 23092 |
| rs535921257 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111157 | GTTGGTGGACATAGA[G/T]GACCCTAATATTCTT | 23092 |
| rs535933180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187818 | ATAAGTGCACTCTAT[C/T]CATTGGGAGCTGTTA | 23092 |
| rs535935752 | snp | C/G | 0.0103295 | 0.0711199 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770586 | GGCCGGGTCCGAGCT[C/G]GGTTCGGGAGTCTTG | 23092 |
| rs535936848 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795861 | TTATGATGGAATGGA[C/T]AGAAATCATGTGACC | 23092 |
| rs535941110 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958509 | CCGTCTTTACAAAAT[A/G]TAAAACAAATTAGCT | 23092 |
| rs535946106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050330 | TCTCGTCCTGTAACC[G/T]TTTTTGTTCTTCTTC | 23092 |
| rs535962574 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140844 | AATTTTTTTAGTTCC[A/G]TTAATTCATCCTAGA | 23092 |
| rs535962896 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132856 | ATTTAAAAAGGAATC[C/T]GGGGTAAAAAAAAAA | 23092 |
| rs535968706 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143197440 | TTCTGGTGGGTGTGC[A/G]GTAACATCTCACTGT | 23092 |
| rs535972819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142782703 | GATTTGACCTTTGGA[A/G]ATGAAACTGGAGAAA | 23092 |
| rs535972870 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164700 | ATAGCTAGCTCTGAA[C/T]TGGAGCATAGAGAGC | 23092 |
| rs535973007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142774600 | TATTAACTAAAGTCC[A/G]TAATTTACATTAGGG | 23092 |
| rs535973428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142777775 | TTGGGGGCCAGTGGC[A/G]CGGCCAGTTGTGACT | 23092 |
| rs535974682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866790 | AGATGTATGATCAGA[A/G]TGCATGTTATGTAAC | 23092 |
| rs535979902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818903 | CCCTATGATAAGGTT[C/G]AAGCCCTACCCTCTT | 23092 |
| rs535982230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043194 | CAAGCACATACCTCA[C/T]TTCCCACCTTGCACC | 23092 |
| rs535984486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863452 | CACATAACTCTCCCT[A/G]GGTTCACATGTATAG | 23092 |
| rs535985422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905167 | ACTTGAAAATATAAA[G/T]TTTTAGGACTCTAAA | 23092 |
| rs535990097 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224263 | GAGGGGAGGCAAAGC[C/T]GAAGAGAGTCAAGGT | 23092 |
| rs535997236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096773 | TCTAGATTCATGCGA[A/G]GCATCACAGTTCAAC | 23092 |
| rs535998229 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815941 | CTGGGACCACAGACA[A/T]GCACCACCATGCTTA | 23092 |
| rs536004819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026181 | AGACTTTTGGCCTGT[C/T]GGCTCCTTGTGTTTT | 23092 |
| rs536008481 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093991 | GAAGTTCAACGCCCC[C/G]CCATGGGGATTTCTC | 23092 |
| rs536008762 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880602 | GAGAAGATGTTTTCA[C/T]TGGAATCAATGAAAG | 23092 |
| rs536009059 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950397 | AAACTAGTGGTGGGA[-/T]TTTTTTTTTTTTAAG | 23092 |
| rs536011862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142980450 | CTGGAGTGCGGTGGT[A/G]CGATCTAGGCTCACT | 23092 |
| rs536014248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116849 | ACTGCCTGAAACATG[A/G]GGTACCTATACCTCC | 23092 |
| rs536025760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793606 | CTTTTTCTTTTTTTC[A/G]AGACAGAGTCTCACT | 23092 |
| rs536028346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977187 | AGAAAGAACAGATGT[C/T]CCTCATAATGAGCAA | 23092 |
| rs536030166 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908070 | ATATACAATATCAAG[C/T]GTATCAAATATTTTT | 23092 |
| rs536032877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966848 | TGTTTTAGCCAACAG[A/G]GCAATAAGTAAACTA | 23092 |
| rs536034798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926963 | CAGCATGCCCTGAGG[G/T]GTAATCCTGGTAACG | 23092 |
| rs536034972 | snp | C/T | 0.0103295 | 0.0711199 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227271 | AAACCAAACAGCCTC[C/T]TAGCTACCTGACTTT | 23092 |
| rs536035040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158992 | GGGTTTATTAACAAA[A/T]GAGTTGGTGCCGAGG | 23092 |
| rs536040927 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076113 | AAGGTGATCCTTACC[C/T]TCCCAAGTAACTAGG | 23092 |
| rs536044711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153024 | TGTGAGTTTGTGACC[A/G]CGGAGTCATGGGCAG | 23092 |
| rs536050768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159648 | TGTAGGGTCTGAGTG[A/G]TGGTATGTTTCTGAA | 23092 |
| rs536055983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987597 | AAGGGAATGCTTCCA[A/G]TTTTTGCCCATTCAG | 23092 |
| rs536065524 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936096 | CAATTGTCTATGTAG[A/C]AAATCCCAAGGAACA | 23092 |
| rs536073270 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201545 | TTGTTTATTTATGTA[C/T]TTATTTTTGTCTGCC | 23092 |
| rs536083983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066249 | TATACCACAGAGCCT[A/T]GGTGTGCAGCAGGCT | 23092 |
| rs536112853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855156 | GAAGTCACCGTTTTA[A/G]AACATAAATGCTCTC | 23092 |
| rs536115598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932808 | ATTGACTATAGAACT[C/T]TTTGCGTCAGGCTGG | 23092 |
| rs536122762 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844995 | CCTCTGTGAGGACTG[C/G]AGGGATGCACTTCCT | 23092 |
| rs536127909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804799 | GCCCGGGCTGAACAG[A/G]TTTTTTTTTTTAAAC | 23092 |
| rs536129737 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030192 | GAGGGGCTCTTGAGC[C/G/T]TGAGGAATCAGGTCT | 23092 |
| rs536129988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036812 | TTATAGACCACTTAA[G/T]TTGTGCTTTTTGAAG | 23092 |
| rs536141799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887398 | TATCTGTCCTACTTA[C/T]GTTATACATGAGAAG | 23092 |
| rs536152757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123458 | TTTCTGGAGATAACA[C/T]TTTGTATAAACTCCC | 23092 |
| rs536168459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214917 | TTAAGCCTTTGCTCC[A/G]TTAACTTTCATCTAG | 23092 |
| rs536185469 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142901583 | ATGATGTTCTCAGCA[A/G]GTGGTGAGGCCCACA | 23092 |
| rs536190276 | snp | A/G | 1.65715e-05 | 0.00287845 | missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142894263 | AAGTGGACCTGGTCC[A/G]GCAGCATTTCTATGA | 23092 |
| rs536191431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986974 | TTGGCTTAGGATTGT[C/T]TTGGCAATGCGGCTC | 23092 |
| rs536193990 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804502 | TTATTTTTTATTTTT[A/G]TTTTTTTGAGACCGA | 23092 |
| rs536195824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811490 | CCGTCACGTGTAGTT[A/G]GTAAGTACCTTATCT | 23092 |
| rs536200383 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172301 | GGCTTGTTACTCTTT[A/T]AAAAAAAAAATACAT | 23092 |
| rs536209039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119226 | CGGGGAAAAATGATC[A/G]TCATCCAAACCGTGT | 23092 |
| rs536209706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179463 | CTTTCTGCTCTGCTG[C/G]CTGTGATCACTGCTC | 23092 |
| rs536214117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982918 | TGTCCTGATGTGACC[A/G]GGAAGCAGCTGTCCA | 23092 |
| rs536217198 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028783 | CATTCAGTTTCCACT[A/T]CCTACAATTCTGTCT | 23092 |
| rs536217438 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205523 | AGGGTAGGTATCTAA[A/G]GGAAACACATGAATC | 23092 |
| rs536218817 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143204697 | AAAAACATTTAGAAC[A/C]CACATTGTGTTCACA | 23092 |
| rs536222375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142995474 | GAGATACCATCTCAT[G/T]CCAGTTAGAATGGCA | 23092 |
| rs536229646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795296 | TGACCACCTCGTAGG[A/G]TTATTGTGAGGATTG | 23092 |
| rs536230496 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094469 | AGAGAACCAGAGACC[A/G]CCCCCAGAGGGGAAC | 23092 |
| rs536231920 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990303 | GTGGTTTTCAGCTCC[A/T]TCCGGTCATTTAAGG | 23092 |
| rs536238189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142858324 | GGTTTTAAAATAATA[C/T]CAGTGGTACCTTGAA | 23092 |
| rs536238436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087243 | GGTGTTGTAAGCCTC[C/T]CCTGTTTTCTCACAC | 23092 |
| rs536245503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989465 | TAATTGGAGCATTTA[G/T]CCCATTTACATTTAA | 23092 |
| rs536249570 | snp | A/G | 0.00011557 | 0.00760076 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014150 | TAACCTTCTACAGCC[A/G]GGGTTGGGAGTAGGC | 23092 |
| rs536251661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021994 | GAGAGAGTATATTTT[A/G]AATTACCATCTAGAC | 23092 |
| rs536274526 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958811 | CAGTGGCTCATACCT[A/G]TAATCCCAGAGCTTT | 23092 |
| rs536276416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087978 | CTTTAGAAGAGTGAG[C/T]CCTTCTCAAACATGA | 23092 |
| rs536277642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126719 | GTGGACTCTCCTTGA[A/G]TTATATGAGAACTAA | 23092 |
| rs536284396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143071134 | TATAGACCAATGGAA[C/G]AGAATAGAGAACCCC | 23092 |
| rs536301023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956075 | AAACCAGGCATTGGT[A/G]TTAAGCATAATTGTG | 23092 |
| rs536302179 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142864040 | TATCTCCACCCACCA[A/G]CCCCTACCGGTTTTT | 23092 |
| rs536307954 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086363 | TTATTTTTAGAGTCT[C/T]ATACAAGCAACTTTT | 23092 |
| rs536335007 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223553 | TCTGCTCCCACCCTT[G/T]CCTGCCTCTAACCCA | 23092 |
| rs536344588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209819 | CAGAGTTGGACTAAA[C/T]GTGTGTGCCCAGATG | 23092 |
| rs536347113 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216356 | GATCTTTGAAAAACG[G/T]AAATGGCATTAAAGC | 23092 |
| rs536355762 | snp | C/G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821965 | CCATAAAGGGCTGAC[C/G/T]CAGCCCTTTGAGGGA | 23092 |
| rs536359313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945811 | AAATTAACACTGATA[C/T]AATATTATTATCTAT | 23092 |
| rs536368462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962641 | TTGTTTGTTTTAAAT[A/G]TCTGGTTGATAAGCT | 23092 |
| rs536379093 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883386 | AGTCAAGTCTCTTGC[A/C]TGTACCCTCCTCAAA | 23092 |
| rs536385922 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989007 | AAATGTCTTTTAGGT[C/G]TGCTTGGTGCAGAGC | 23092 |
| rs536392701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185144 | TTTATTAATATGGGG[A/G]TATTACATAACAAAA | 23092 |
| rs536418876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985351 | TAAATAACTTTAGTG[C/T]AGCCTAAGTGTACAG | 23092 |
| rs536424584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206537 | TTGAGTATCGTAATG[C/G]CCAAATTCCACGAAA | 23092 |
| rs536428027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911711 | ATATCCCTATTCCCT[C/T]CCATTTCTCTGGGAC | 23092 |
| rs536436504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009293 | ATCTCACCTTTATCA[C/T]CGTCAGCATCATCAT | 23092 |
| rs536440966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838106 | TACTAAAAATACGAA[A/G]ATTAGCTGGGCATAG | 23092 |
| rs536444533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822725 | TACAGTAAAGCATTC[A/G]AATGGTTGGATTGTG | 23092 |
| rs536451197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845718 | TCTGGCTGGTGTCCA[C/G]ATAACTGGCGGCCCT | 23092 |
| rs536455238 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905344 | TTATCATGAGGACAC[-/T]TTTTTGTTCCCTAAC | 23092 |
| rs536462863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781950 | TCAATCTCCTGACTT[C/T]GTGATCTGCCCGCCT | 23092 |
| rs536468983 | snp | A/G | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966519 | TTTCCTTTCATGAGT[A/G]TGAATAATAAAGTGT | 23092 |
| rs536478725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142870222 | TTCTCTCTCCTCTTA[C/T]TGGAATGTGTGTGTT | 23092 |
| rs536485906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877272 | TAAGCTCAGCAAGCA[A/G]AGCCGCACCTTCTCT | 23092 |
| rs536491012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146708 | GAAAGGGTCAGGAAT[G/T]TAGACTGGTGGAGTC | 23092 |
| rs536494277 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999623 | GCTGCTGTGGGGGTT[-/A]AAAAAATATCAAGGT | 23092 |
| rs536503609 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925270 | GCTTTGCACTTGCAC[G/T]GTTGTTTTTCCCACA | 23092 |
| rs536521417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852368 | TCCTCACAGGCATTG[C/T]TGAGTTCTTTACTAG | 23092 |
| rs536529113 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091319 | TGATCCTCAGGCTGG[C/T]GCTATTTACCAGAAA | 23092 |
| rs536533005 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961833 | GTCCCATTTGAAGTG[-/T]TTTTTTAGTTCTTCT | 23092 |
| rs536542129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804878 | TCTCACCATCATGCA[A/G]CCACTAATCTGTGTT | 23092 |
| rs536546579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198479 | ATATTAAGGTCAATA[A/T]GTATTGTGAGCCACG | 23092 |
| rs536547946 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142876663 | CGTATGCTTGTAGTC[C/G]CAGCTACTTGGGAGG | 23092 |
| rs536552268 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912620 | TCTTTTCTAGGATCC[A/G]GTTGGGCCCAGGAGA | 23092 |
| rs536557133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948691 | AACAGAGGTTAGAAG[C/G]GGATATAAAGCAAGA | 23092 |
| rs536560605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875908 | ACTGTGCCTAGCTAA[C/T]TTATTTTTGTTTTTT | 23092 |
| rs536561896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212778 | TTTGCAGAGAAAGTT[G/T]GCCACCTTCTGCTCT | 23092 |
| rs536591430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983706 | AAAATAACTAAAAAG[A/G]TGAAGAGGAAAATGA | 23092 |
| rs536594530 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933916 | ATGGAGATAAAATTT[A/G]AAATTGCCTTCGAAA | 23092 |
| rs536598344 | in-del | -/AA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212371 | AAAAAAAAAAAAAAA[-/AA]TGCCTCTTATATTCC | 23092 |
| rs536613041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887201 | CTGGAATGAGTCCAG[C/T]ATTTTCTTTTAGGGC | 23092 |
| rs536615359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979717 | CCAGGCAAAGAGAGT[A/G]TTTGTGTGAGAATTA | 23092 |
| rs536615733 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170581 | ATAATGGTGGTAATG[A/G]CAATGATAATTCACA | 23092 |
| rs536623975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201758 | TGTACTCTCTATTTC[C/T]TGTCTGTTTACAGTC | 23092 |
| rs536634659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142840647 | GTCATCGTCTTATTT[A/G]AGCCTAGTTGGTCAG | 23092 |
| rs536642833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067933 | CTTGGGGAGGCCAAA[A/G]CAGGCAGATCACTTG | 23092 |
| rs536643322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147699 | GTAAGTTTTACAAAC[A/G]TCCAGGGACTGTAGC | 23092 |
| rs536643740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844038 | AGTATCATTACATGT[A/G]AGCTAAAAGTGAGTT | 23092 |
| rs536648433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070789 | GTGGTGTGCACCTGT[A/G]GTCCCAGCTACTCTT | 23092 |
| rs536649148 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142915695 | AGGAGGTAAGTAGAC[C/G/T]GTCCTAGGAAACACC | 23092 |
| rs536652359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847605 | CAGGTGATCCGCCCA[A/C]CTCGGCCTCCCAAAG | 23092 |
| rs536652873 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202905 | TGGACCCCTTCCTTA[C/T]ATTTTATACAAAAAT | 23092 |
| rs536654575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157700 | CTCATAATGGATGGC[A/C]TTACTATGGTAGAGA | 23092 |
| rs536655738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850955 | ATATGCAGTGTCAAC[C/T]AGGCCACAGGAAGAT | 23092 |
| rs536664441 | in-del | -/CAGATGTGTG | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851236 | GAGTAGTTGGGATTA[-/CAGATGTGTG]CAGATGTGTGCCACC | 23092 |
| rs536680264 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037111 | GACCACAGCATGCGA[A/C/T]TGATTCATCCTGGTT | 23092 |
| rs536687196 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012761 | TGGGTTCATGCCATT[A/C]TCCTGCCTCAGCCTC | 23092 |
| rs536694054 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070713 | TCAGGAGTTCCAGAC[C/T]GGCCTGGCTAATATG | 23092 |
| rs536716452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938605 | TAGAATAGAATTTCT[A/G]CCAGCCCATCATCAT | 23092 |
| rs536726467 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099828 | TTCCATTGAGACCAT[A/T]AAATAGTTATGTTTC | 23092 |
| rs536733053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034883 | GGAAGAATTATTTTA[A/G]TTGGGCTTTCAGCCT | 23092 |
| rs536740162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143039260 | TTGCTTAGGCTGGAG[G/T]GCAGTGGCTCAATCT | 23092 |
| rs536753260 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060970 | GGAGATTTTATTGTC[A/G]TGATTAAATTAGCTT | 23092 |
| rs536771232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035581 | AAGCCTACAAATAGG[G/T]TGCTGTGTATACTGC | 23092 |
| rs536777233 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163461 | TTTGTTTGTTTGTTT[G/T]TTTTTTTAAGATGGA | 23092 |
| rs536794425 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163930 | AATGACATAGAAAGG[-/A]AAAAAATATCACAAA | 23092 |
| rs536794629 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941817 | AGTTGATGAAATTTT[C/T]TAAGAAATGGAAATT | 23092 |
| rs536805741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969203 | ACCTCAGCCTACCAA[A/C]GTGCTGGGATAACAG | 23092 |
| rs536808379 | snp | C/T | | | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966352 | TTTTTTTTAATTTTC[C/T]AGAGTACTTTGACAT | 23092 |
| rs536812353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096935 | ATAATATCCTCATTC[C/T]AGCCACCTCTTAAAA | 23092 |
| rs536817496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103554 | CAACCCAAATGCCCA[A/T]GAATGTTAGACTGGA | 23092 |
| rs536829573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015408 | GGAGACCTAGGAACC[C/T]GGTGAGAAAGGGTCT | 23092 |
| rs536832792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918837 | CTTCAATCTCAAACC[C/G]AAAACTTGCTTGGAT | 23092 |
| rs536835308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830112 | TGTTGGCCAAGCCTC[A/G]GGAACATAGCACGTG | 23092 |
| rs536835391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143146099 | GATTAGCCTAGATAT[C/G]ATGTTTAAGTGAATT | 23092 |
| rs536846693 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175090 | ACTTTCTTTTCCCCA[C/T]ATAAAAGGAGCCCAA | 23092 |
| rs536852427 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227616 | CTTTTTTTCTCCTGC[C/T]GCCTACAGTACCTGT | 23092 |
| rs536853968 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829445 | ATCACCTTCTTTTCC[A/G]CCCAAATTAGCAAGA | 23092 |
| rs536858094 | in-del | -/AAATAAATAAAT | 0.0239832 | 0.106848 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105379 | GAAGCTCCATCTCAA[-/AAATAAATAAAT]AAATAAATAAATAAA | 23092 |
| rs536880204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142780876 | GCTGGTGAGGGAGTC[A/G]GGAGTTTTGCATGAC | 23092 |
| rs536881147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874033 | CTGACCTGGCAGCAG[C/T]TGGCTGAGCTATGCG | 23092 |
| rs536888432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057318 | TGAAATGAAGTCTTC[C/T]CTCTAGGGAGCCAGC | 23092 |
| rs536893006 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049705 | TCATTATCTTACCTG[A/G]TGATTGGAGGGGTAT | 23092 |
| rs536919320 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935810 | TACTTACTCTCAGAT[A/G]TATGTTCCTTTAAAT | 23092 |
| rs536919888 | in-del | -/TTTTTTTTTTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029412 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTT]GAGGCAGGCTCTCAC | 23092 |
| rs536925662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151907 | GTTGCAGTGAGCTGA[A/G]ATCGTGCCACCGCAC | 23092 |
| rs536932787 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001163 | GAACAGTGGTTGCCA[A/G]TGCATGGGGTGTGTG | 23092 |
| rs536936404 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150348 | AGCTAAGAAAGAAAG[A/G]CAGTGGCATATGGCA | 23092 |
| rs536938894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109892 | TCACTCAGTCAAGAA[C/T]AAAGCTTTTACAGTG | 23092 |
| rs536943541 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210859 | GATCCCAACTTGTTC[A/G]TGCCCTTAAAGGCCC | 23092 |
| rs536946770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142873335 | GAAGGACCAATAAGG[G/T]CAGCAAATCAGAAAG | 23092 |
| rs536950466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056629 | CTGGTATTAAAATAC[A/G]TAGGGATTAGGTGCA | 23092 |
| rs536950467 | snp | G/T | | | intron-variant, missense | ARHGAP26 | GRCh38.p7 | 5:143166041 | GGCACTGGGGATTTG[G/T]AATGTGTTTGGAGGG | 23092 |
| rs536955412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880433 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 23092 |
| rs536957000 | in-del | -/AGGG | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072789 | GGGGAAAGGGAGGAT[-/AGGG]AGGGAAGGATTTGTT | 23092 |
| rs536985638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793189 | AGGCTGAGGCTGGTC[A/G]CCAAGCAACCCTGGA | 23092 |
| rs536989886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187881 | TCTTGCCTCAGCAGA[A/G]AGAAACATTTTGCTC | 23092 |
| rs537003164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824481 | GCCCTAGCATCAGCA[G/T]CTGTATAAGCTCCAG | 23092 |
| rs537006341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115939 | TATAGCAGTATTTCT[C/T]AAATAGTAGTTCACG | 23092 |
| rs537006815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186167 | GGGAACTGTTTGTCA[C/T]TCACCTTGTGGAATA | 23092 |
| rs537014371 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889456 | TGTCTCTAGTGAAAA[C/T]GCAAAAAAAAAATTA | 23092 |
| rs537018517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142800611 | CAGGTGATCCACCCA[C/T]TCAGCCTCCCAAAGT | 23092 |
| rs537021176 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067377 | ATGGATTTCCTTTCC[C/T]GAGTTACTGAAATCT | 23092 |
| rs537027004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142792505 | GATGCCCTGTTTGGC[A/G]ACATCTAAGCACTAG | 23092 |
| rs537032041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147982 | CTGGTTGTCTAGCCC[C/T]CCACAGAAACTAGGT | 23092 |
| rs537038984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929226 | GATGTTAGTCACTGC[G/T]CCCGGCCTATCCTCC | 23092 |
| rs537049843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143076039 | AGCTCTCACTCTGTC[A/G]CCCAGGCTGGAATAC | 23092 |
| rs537051837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018397 | TGATTTTCAAGTTGT[A/G]TTTTGGAGAAGGCCT | 23092 |
| rs537054025 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142839766 | ATGAAATGGATGGTT[A/C]AGGGAGAAAGTGGCA | 23092 |
| rs537064839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824006 | GTAAAAGTTTGGGGA[C/T]GACTTCACTTATTTT | 23092 |
| rs537086492 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, synonymous-codon | ARHGAP26 | GRCh38.p7 | 5:143068423 | CCACAATATCCACAC[C/T]TGTGCCTATGTTTCT | 23092 |
| rs537103316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791110 | TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCAGGC | 23092 |
| rs537115209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847094 | ACCTTGGGCAAATCA[C/T]TGTGCCTCTCTCACC | 23092 |
| rs537116667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153465 | ACAGTGACCAGTGGG[G/T]CATCATGCCAACTCC | 23092 |
| rs537123953 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935192 | GTCTGTGGCTCATCC[A/G]AATCTGGGAACTTAC | 23092 |
| rs537130564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799847 | TGGCCTCATCACCTC[C/T]TAAAGGTCCCCACCT | 23092 |
| rs537130833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129008 | GCATGTGACAGATGG[G/T]ATTGAAGAAGGTCTA | 23092 |
| rs537133825 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886238 | GGCCGGCCCTTTTTT[A/T]AAAATTTTAATTCTT | 23092 |
| rs537139386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963715 | GCACTTTCCCTCTTC[C/G]CAACCTCTAGAACCT | 23092 |
| rs537149526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058751 | GTCAAGCACTTGATA[C/T]TGCCTTTGGGAAAAA | 23092 |
| rs537153878 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811513 | CCTTATCTTTTTCAT[A/G]TATTCAACAAAAAAA | 23092 |
| rs537166899 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143097586 | AGCACTTTGGGAGGT[C/T]GAGGCGGGTGGATCA | 23092 |
| rs537169436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032629 | GGGAATTTGCTTTTC[A/G]GACTAGGAGATCTCA | 23092 |
| rs537177859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830951 | AGGCAAATATGACCT[C/T]GCAGATGAGCTCCTT | 23092 |
| rs537178279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970185 | CACATATTCAGCACT[C/T]GTGAACCAGGCCTTC | 23092 |
| rs537178736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142838606 | TTTCAAGATGGTTGT[A/G]ACCATTAAAAATAAT | 23092 |
| rs537181192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167412 | ACTTGAACCCGGGGG[A/G]GAAGAGGTTACAGTG | 23092 |
| rs537194984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193648 | ATGCTAAAGAGAAGC[C/T]GTAAAGTGCTTCCTG | 23092 |
| rs537200188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958545 | TGGTGGCATGTGCCT[A/G]TAGTGCTAGCTACTT | 23092 |
| rs537208337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188688 | TTTGAAAGTGTAGAC[C/T]GATGATTTCTGAAGG | 23092 |
| rs537209898 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837358 | AATTCTGTTTTTTTT[C/T]TTCACCCTCTCCCTC | 23092 |
| rs537213060 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812577 | TCCTAGCCTCAAGTG[A/T]TCCTCCTGCCTCGGC | 23092 |
| rs537224590 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880047 | ATATTACCCATTGTG[A/C]AGGTCAAAAAATGAC | 23092 |
| rs537232526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853701 | ATCGTTGTCTATCAT[G/T]ATGTTGAAAATCCCT | 23092 |
| rs537232744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089418 | CATGCTGTAAAGGGG[C/T]CATTTACCCCTGAGT | 23092 |
| rs537233124 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149623 | TCTGAGAAATCTGTC[A/G]GCACACAGACGTGCC | 23092 |
| rs537233271 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908670 | AGCCCTCTCAGTTTC[A/C]GTGGGGGAGGAGGTA | 23092 |
| rs537262699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182006 | GCTTATTCTTGTCCC[C/T]GTACAAAGCACATCC | 23092 |
| rs537263350 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142883099 | TTTTCTCAGGACAGA[A/G]ACGGCTTCCCTTTCT | 23092 |
| rs537282834 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054314 | AATAGGTAAAAAAAA[A/T]ACTTGTCATTTTTGT | 23092 |
| rs537287165 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867551 | GGAGAAAGAAAAGAG[C/T]GATCTCTGGGGACTC | 23092 |
| rs537296296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950859 | TGTCAAGAGAGCCCA[C/T]CTTGCTTGCAAACCA | 23092 |
| rs537305458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060753 | CTACTCAGTCAGGCT[C/T]GCTGCCTGGGAATCT | 23092 |
| rs537312817 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888450 | TCTCGTAGGGGTCAG[G/T]TGTTTTGCTCAAGGT | 23092 |
| rs537319201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044719 | AAGTATATCTAATAC[A/G]GATGTAACAATATCA | 23092 |
| rs537327297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949779 | AGGATCCATGGATCA[A/G]TATGGACAGGGGCAT | 23092 |
| rs537332923 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142834240 | TCACACAGTGAATAC[A/C]CTTATGTAATGGCAA | 23092 |
| rs537344410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061698 | TGTGTCATGACACAG[A/C]ATCTGTCCTGAGAGT | 23092 |
| rs537347557 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120101 | GGGAAGCTCTTGATA[G/T]TGTCTCAACAAAACT | 23092 |
| rs537362080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038100 | GAAAAGCTATTAACC[A/G]TCTTTCCACTGGATT | 23092 |
| rs537366137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219468 | AAGCAAAGCTTAGCA[C/T]GTTTGAACAGCATAT | 23092 |
| rs537381946 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142972324 | GCCATTTAAGATGCT[G/T]CTTTGCTCAGAAACC | 23092 |
| rs537383954 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890882 | AGCTAGGACATTGTA[A/G]CATTGGAGCTTGCAC | 23092 |
| rs537387177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088784 | CCCTGCCGCTGTGTC[A/G]TTCCCCTATTGGCTA | 23092 |
| rs537388533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914194 | TGAGTACTGCCTGGG[A/G]TTGCACTGCCTTCTT | 23092 |
| rs537391111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180503 | GTGCATTTTGTCACT[G/T]CTATAAAGAAATACC | 23092 |
| rs537396384 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195599 | AGACCATTGATTTAC[A/T]GTAATAAGTTTCCCA | 23092 |
| rs537400091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143191120 | GGATGATGCTTGCAC[A/C]GCTCCATCAGTATTC | 23092 |
| rs537407682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183386 | GAGATAATGAGAGCC[A/G]TGTGCTCCGTGACCT | 23092 |
| rs537410723 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816568 | AAGAGGAGTTGAGTC[A/G]GAAGAAATAGGAAGA | 23092 |
| rs537416313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847599 | GGACCTCAGGTGATC[C/T]GCCCACCTCGGCCTC | 23092 |
| rs537426939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911032 | ATTTGGATTATTTTC[C/T]TTTAAAAGTACCCAC | 23092 |
| rs537429512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011101 | CCTTATCTCCTACCC[C/T]TCTCTGCATTGCACT | 23092 |
| rs537457503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102248 | TTCTCTTCACTTCCT[A/G]CCTTCCAGGCCTGGG | 23092 |
| rs537463305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142917159 | ATTCTCCTGCCTCAG[C/T]CTCCTGAGCAGCTGG | 23092 |
| rs537466318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143010612 | ATTAACCCAAACCAG[A/T]CAGAGATTAACAGCC | 23092 |
| rs537466536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821437 | CTGCAAGTGCACTCT[C/T]ACATTTTTCTAGGTG | 23092 |
| rs537466587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828538 | CATTATTCTTTTCCC[C/T]CTAAGGTTTTTGCCT | 23092 |
| rs537477252 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002106 | CATCAGCCTCGAGTT[G/T]CAATGAAGACAGCTA | 23092 |
| rs537486638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056511 | TGTTTCCCTGAATAT[A/G]ACACCATTTATATAA | 23092 |
| rs537493198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783478 | GTAATTATGTTTCAC[A/G]TTTTTTTTTTCTTTA | 23092 |
| rs537503560 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009926 | TCCGCTTGGGTTGCT[C/T]CTGGAGAGTTGAGTT | 23092 |
| rs537525530 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844701 | ACATCCTGTCAATAT[A/G]AAAATTAGCCGGGCC | 23092 |
| rs537533959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107712 | CCAGATCTCGACTTC[A/T]CTCTGAATCGTTCGG | 23092 |
| rs537536795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967840 | GTGCACGGATATGAA[C/T]GATGGCAGCTGGGAG | 23092 |
| rs537543470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970836 | GGAAGAGGATGTGAC[A/G]GTCACTCTAGAAAGG | 23092 |
| rs537550030 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878273 | AAACTGTAAAATATT[A/G/T]TACTGCCTTAGAAAA | 23092 |
| rs537573524 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183363 | CTGATCTTATCGTGG[A/G]GATTGAGGAGATAAT | 23092 |
| rs537574211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142828100 | GTTTCCCTGGATCAA[A/G]TTTCCTCTACAGGTA | 23092 |
| rs537574282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977980 | GTTGACAGATCACTT[A/G]CAAAGCCATGGGAAA | 23092 |
| rs537576878 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142948329 | GATGGGTGTGCATGT[A/G]TGTATATATGAATAT | 23092 |
| rs537581078 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218636 | GTGGTTGGCAGGAAG[C/T]TCACCCATGTCCCCA | 23092 |
| rs537589057 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992571 | TAGCTGGGACTACAG[G/T]TACCCGCCACCATGC | 23092 |
| rs537590057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016945 | TTTAATGCAAACCCC[C/T]CATAAGGCTCATCTA | 23092 |
| rs537590578 | snp | A/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869382 | CCGGCTATTTTATTT[A/T]ATTTTTTTTTGTATT | 23092 |
| rs537590879 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027891 | TGATGCATAATTGCC[A/G]GGAGAGGGCCCAGAA | 23092 |
| rs537599061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900765 | GTTTAACAGGTTAAA[A/C]AAAAATCATTTAGGG | 23092 |
| rs537618049 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989576 | TTCCTAGCATCAATG[G/T]TCTTTACAATTTGGC | 23092 |
| rs537622131 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790753 | ACTGTTCCTCTGGAA[A/T]GCCTTTGCTACAGGT | 23092 |
| rs537625508 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086374 | GTCTTATACAAGCAA[C/G]TTTTGCCAGCACACT | 23092 |
| rs537625668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851152 | GCCCAGGCTGGAGTG[C/T]AGTGCATGATCTCGG | 23092 |
| rs537628490 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903720 | TCAGGCCTCTTACCT[A/G]GAAGGTGGAGGATGT | 23092 |
| rs537628885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991699 | CCTACAGTATTCAGT[A/G]TGGTAACATGCTGTA | 23092 |
| rs537648983 | snp | C/T | | | intron-variant, missense | ARHGAP26 | GRCh38.p7 | 5:142919254 | TACACGAGAAGATAC[C/T]GTGTTAACATGAAGG | 23092 |
| rs537659995 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900321 | ATGGGGCTTACCACT[A/C]ATTCACGGATTTATG | 23092 |
| rs537674521 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956019 | ACTCTTAAAGACAAC[-/AG]GGAATTATCTGAGAA | 23092 |
| rs537679031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, splice-donor-variant | ARHGAP26 | GRCh38.p7 | 5:143216834 | TGGACCTGACAAAAC[A/G]TTAGTACACTTTCTC | 23092 |
| rs537687039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850545 | TTGCATACAAACTTT[C/T]GAAGTTATTAGCTAT | 23092 |
| rs537701386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134579 | CTTTCATGGTGCCTG[A/G]CATGGAGTCGACACC | 23092 |
| rs537711148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142232 | CAACCTTCGCCTCCC[A/G]GGTTCAAGTGATTCT | 23092 |
| rs537712889 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143355 | GCCATTAGAGTGGGT[C/T]GGAGTCACTTGGTAA | 23092 |
| rs537716655 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041570 | AAGGAAAGCTTCTTT[C/T]GCCGCTGATGACTGA | 23092 |
| rs537726218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809443 | TTCTTCCTGTTTTGG[A/G]CACTAGCAATCAAGA | 23092 |
| rs537726614 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049355 | GCTGTTTATAATGCA[A/G]ATTTTAACTTTTTGT | 23092 |
| rs537727219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812158 | GTATGAGGGTTGTTC[A/G]GGCAGACATCCTGAC | 23092 |
| rs537730065 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226322 | CCGTCTCTACTAAAA[A/C]TACAAAAAATTAGCC | 23092 |
| rs537754984 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791909 | GCGGAGGTTGCAGTG[A/G]GCCGAGATCACAACA | 23092 |
| rs537765137 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042374 | AACCAGAGAAATCTT[C/G]TGATCCTCTTTGCTT | 23092 |
| rs537766559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776982 | GTGAAGTGGTATCTC[A/G]TTGTGGTTTTAATTT | 23092 |
| rs537781853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178379 | CTCTTTCTGTTGAAT[C/T]AGTACCCAGAAGAAG | 23092 |
| rs537788767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817914 | ATCAGAGTTTTAGTT[A/G]TGATTCATTTGTGAA | 23092 |
| rs537788807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095999 | ATTCTTTTTTTAAAA[C/T]TCTACCAACATTCAA | 23092 |
| rs537789552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815256 | ATGTTGGCCAGGCTG[A/G]TCTCAAACTCCTGAC | 23092 |
| rs537790979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004473 | AAACCCCAAATGCAG[C/T]GAAATTAATCAGCCC | 23092 |
| rs537801876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041006 | TTTGGCTACTGGTTG[A/G]AGAATGGACATCAGA | 23092 |
| rs537802670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033593 | ATCACTGTCAGATGC[C/T]AGGTTCTTTTCAATT | 23092 |
| rs537804247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903123 | TCCCCTTTTAAGGAG[A/G]GACTCATCTGTGAGC | 23092 |
| rs537804329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895128 | AAACTCTCGCAGACC[A/G]TGGATTTTCCAGCCA | 23092 |
| rs537809469 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143229180 | TTTCCATTTAGGAAG[A/G]GGTCAGATGCTAGGA | 23092 |
| rs537809474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105901 | TTTCCATTGCCAAAT[A/G]GAGAAGAGACTTTTT | 23092 |
| rs537824469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993209 | GCTCTGTCGCCCAGG[A/C]CGGACTGCGGACTGC | 23092 |
| rs537841621 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031369 | AAGAAGACCAGCCAG[C/G]AGGTTAATGCAGTCA | 23092 |
| rs537843028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168537 | CACACAAGATCTTAC[A/G]ACATTCTGCATCATC | 23092 |
| rs537845317 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098978 | AGTGGCTTCAAAAGA[A/G]GACAGCAGAGGCTTG | 23092 |
| rs537851251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773027 | TGTTCTGTTCTCTCT[A/G]CGTCCAGCTCTGCTA | 23092 |
| rs537860732 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999306 | GCCTCGAGCATATAG[A/C]TCTTTACAATGCTCA | 23092 |
| rs537866774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902354 | AAATCCCAGCCCAAC[C/T]CAGCCTCCATTCTAT | 23092 |
| rs537871920 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027766 | AGGGAATGTGGTATA[C/G]ATACTGGCAATTGAC | 23092 |
| rs537875934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142869454 | TCGAACTCCTGACCT[C/T]ATGATCCACCCGCCT | 23092 |
| rs537880460 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074073 | AAATGGTGGTAAAAC[-/TT]TTTATCTTAAAAAGG | 23092 |
| rs537885733 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833329 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCATGA | 23092 |
| rs537894841 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138436 | CAAACCATCAGGAAA[C/G]CACTGAATATTTTAG | 23092 |
| rs537903741 | snp | C/T | | | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862928 | TGAGACTAACAGAGT[C/T]TGTGTTCTCTCAATT | 23092 |
| rs537912553 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024382 | TGCCATGGCCTAATA[C/T]TCCCCTTTCCCTCAG | 23092 |
| rs537921072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196944 | GAATTTGCAAATAAG[A/G]AATATGGAAATAATG | 23092 |
| rs537930751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813701 | ATCTTCTTTTCTTAT[A/C]AGGTCACCATATTGT | 23092 |
| rs537945681 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048305 | TCACTCTTTCACCCA[C/T]GCTGGAATGCAGTGG | 23092 |
| rs537966296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967196 | TCAGGGCAGGGAAAA[A/C]AGAACGATAAAAATT | 23092 |
| rs537966795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048037 | TCTTTTTAGTAGAGT[C/T]AAGGTTTCACCATGT | 23092 |
| rs537968222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974669 | CTGACTGCAGGGCTC[C/T]GCTCCCGCCTGAGCT | 23092 |
| rs537969847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105309 | TTGAACCCGGGAGGC[A/G]GAGGTTGTGTGAGCC | 23092 |
| rs537971559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129927 | TTGACTGAGATTACA[C/T]AGCTAGTAGGTAGCA | 23092 |
| rs537975126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214584 | CTGCACCTGATTCCG[C/T]GGGTCCTGGCTGCAT | 23092 |
| rs537979563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142868319 | CCAGAGAGGGGTGTG[A/G]GGAGGCCAGACCCTG | 23092 |
| rs537999636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909344 | CAGTACATTTTTATG[C/T]AACATGTTGAGTTTG | 23092 |
| rs538001957 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900384 | TTTATAGCCAGAGGA[C/T]CCAGCAATGCCTACT | 23092 |
| rs538004166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803369 | TTCCCCATTTGGAAT[A/C]TTTTGGCTGCCTTTA | 23092 |
| rs538017028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143027696 | TATGCCAAAGTGGAA[C/T]AATCCAGCATTCCAT | 23092 |
| rs538027496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156589 | CAGATGATTCTGATA[C/T]ATGCTCAAGTCTGAG | 23092 |
| rs538030148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196350 | TCCATTCTTGTTTTT[C/T]GCGGTAGTCATGTTC | 23092 |
| rs538044495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835133 | TGGTAAATCAAGTTT[C/G]ATCTGTACTAAATCA | 23092 |
| rs538047107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904962 | GGACTTAAGTTTCCT[A/G]GTAACTGGGGCAGTA | 23092 |
| rs538047823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923960 | TCCGCCCCCCGGGTT[C/T]GTGCCGTTCTCCTGC | 23092 |
| rs538050189 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163210 | GGAGATCAGATCTAC[G/T]TATGTGGGGGAGCAT | 23092 |
| rs538057843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156903 | GCTGCTTCGCAAATG[C/T]GTGCCTGTTGGTTAC | 23092 |
| rs538058243 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020787 | GGGACTACAGGCACC[C/T]GCCCTCACGCCCGGC | 23092 |
| rs538059152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086989 | AATTCAGTCTGCTGA[A/G]TTTTACGAGCTTGCT | 23092 |
| rs538073963 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125950 | TACTCTCAGAACCCA[A/G]GCTATTAAAATCTAC | 23092 |
| rs538074186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794719 | AGGGGACTGCCCCTG[C/T]TGGGACAGATGATAA | 23092 |
| rs538091867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142856975 | CTGAAATCAGAGTGT[C/T]AACAGGGCCATATTC | 23092 |
| rs538092741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070501 | GATGACAGAAATTGA[A/G]GAGAATACAAACAAA | 23092 |
| rs538094045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142875017 | TCTGTATGTGCCAAG[A/G]AATTAAAATCCATAA | 23092 |
| rs538099883 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837037 | AAATCTCTCGCAGAA[C/T]GCATTTGGAAACCAA | 23092 |
| rs538105724 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981882 | GTTCCCGACTCAGTG[A/C]AAGGCTTCCATTTTG | 23092 |
| rs538105901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863343 | TGAACTCCTGACCTC[A/G]TGATCCGCCCACCTC | 23092 |
| rs538110149 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142779955 | TAGGTAATACCTATA[A/C]GTTGTTCATAATTCA | 23092 |
| rs538110857 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007790 | ATTGATAGTGAAAAA[A/G]TGGTTGGTGGCAGGT | 23092 |
| rs538118436 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142815776 | TAGCCTTCCTGGTCC[A/G]TCTGTGCTACTGCTG | 23092 |
| rs538119721 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032820 | GAGTGGAAATCAAGC[C/T]CTTTGTGTGTGTGCA | 23092 |
| rs538122653 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137877 | GCAAAAGTTGGAGCC[C/G]ACTGTTTGCTCTTAG | 23092 |
| rs538125384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937865 | TGGAATAGTGATATC[C/T]AGGGTATACGGACAT | 23092 |
| rs538130931 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143222533 | ATTTCTCTTTGCCAC[C/T]GAGAAATGCAGCGTG | 23092 |
| rs538135667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888685 | TGGAATGGCACTGCC[A/T]TCTAGTGGATGATTT | 23092 |
| rs538136080 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015528 | TTTGGGTCCACCCAG[C/G]GAAAAACTGTACATT | 23092 |
| rs538142434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034141 | GGAACCCTCGTACAT[G/T]GCGGGTAGGAATGAA | 23092 |
| rs538146666 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818899 | CTGACCCTATGATAA[G/T]GTTCAAGCCCTACCC | 23092 |
| rs538146692 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021241 | GGCATTATGTTGAAT[A/G]TGCTTGTTGTATTCT | 23092 |
| rs538150526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142801477 | TCCATGGGAAAGACA[A/C]TGGATGCCCCTTTTT | 23092 |
| rs538158650 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124971 | CCTCTCTGCATTGCC[A/G]TTTTTTATTCAACCA | 23092 |
| rs538159969 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162108 | CTGAAGCACAAGAGA[A/C/G]ATTTCTTCAAATGAA | 23092 |
| rs538160943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961485 | TGACAAAACAAGACC[C/T]TGTCTCAAAAAAACA | 23092 |
| rs538163252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945107 | TAACTTGTTGTATTT[C/T]CCCCAGTGCTACCAA | 23092 |
| rs538165312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132081 | GTTGAACTCAGCTAC[A/G]TGTAGTGATTCAGTT | 23092 |
| rs538170305 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773545 | ATAGATCTAGATCCC[C/G]TAAAGGAGAAACATG | 23092 |
| rs538172328 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223445 | TTTCTGTTCCTCCAT[A/G]CAACTGATGTTTGTT | 23092 |
| rs538177591 | snp | G/T | 0.275999 | 0.248644 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026816 | GGTGGGGGTGGGGGG[G/T]GGGGGCAAAATTGAA | 23092 |
| rs538189708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895948 | AGATTCCTTAAAGTC[A/G]TCAATTACTTCAGTC | 23092 |
| rs538206010 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030660 | ATCTACTCTCAGAGG[G/T]TTTATATCAGTTGAA | 23092 |
| rs538219801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848878 | CAGCTCTTTCTTTCC[C/T]GCCTACTTGGTTTCT | 23092 |
| rs538220124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084631 | ATCTGGACACTGCTT[C/G]CTCTCCAGCCTCGCC | 23092 |
| rs538230951 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830606 | TGGATAAAAAATACC[A/G]GTCTTCAAAAAATGT | 23092 |
| rs538231625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984584 | GATTCTTTTCTTAGC[A/G]TAATGCATAGAAGTA | 23092 |
| rs538237076 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201222 | GCTGTGTTGTTGCTG[C/T]CATTGGGCCTAGATG | 23092 |
| rs538247350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933793 | ATGTTATTACTTCAA[A/G]GAAGAAGAGGAGAAA | 23092 |
| rs538248213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992671 | TGACCTCGTGATCCG[C/T]CTGCCTCGCCTCCCA | 23092 |
| rs538256557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077659 | ACCATTTCTGGCTTG[C/T]ACAGATGACAGGGCG | 23092 |
| rs538259105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996096 | ACCTAATGTAGGTGA[C/T]GGGTTGACGGGTGCA | 23092 |
| rs538261887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990739 | TCCACTCCAGACCCT[G/T]TTTGCCTGAGTATCA | 23092 |
| rs538263198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899621 | GAAGCAGACAGCTCC[C/G]CCATCTCTGGAGTCC | 23092 |
| rs538270584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215109 | AGTCCTGGCCCTGCC[A/G]TAACATGACACGGCC | 23092 |
| rs538283737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127872 | AAAATTAATAAAAAG[A/G]TATGACTGGATGCTT | 23092 |
| rs538288345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143212865 | AAATACTGATGCCTG[A/G]CCGGGCGCGGTGGCT | 23092 |
| rs538289628 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855255 | GAAGACAGAGAGCAT[A/G]TTTGTGTTTGTGAAG | 23092 |
| rs538301303 | snp | A/T | | | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964431 | GTATCACTTGCTGAA[A/T]AAGGAAACCCTAAAA | 23092 |
| rs538313132 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988662 | TACACACAGCTTTAA[A/T]TGTGTCCCAGAGATT | 23092 |
| rs538313330 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047339 | AGTCATCTATTTCTG[C/T]ATCTGTAATAATGGC | 23092 |
| rs538328997 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117770 | AGAAATGGAACATAG[C/G]TGAAGACTTTGATAA | 23092 |
| rs538330759 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768946 | GTCTTGAACTCTTGA[A/C]CCCAAGCAATCCTCT | 23092 |
| rs538338046 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198169 | TTGTTTTGGCAAGCA[C/G]AATATCTTCATTATG | 23092 |
| rs538344212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114519 | AACTTGTCTGGTTAG[C/T]CACAAAAAAGTGTTG | 23092 |
| rs538347179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127409 | AATGTTTGACAAAAT[A/C]AGTTATAATAATTCC | 23092 |
| rs538362936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142959256 | TTTGTCAAACTTACT[A/G]GACACTCACTTCACC | 23092 |
| rs538373368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182389 | GAAATGTTCTTGCCC[A/G]GTATTTCACTCGTTT | 23092 |
| rs538374440 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169244 | TGTATGTCAGCTTGA[C/G]CAGATTTACCCATCA | 23092 |
| rs538374685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813177 | TGATCTCCTGACCTC[A/G]TGATCCACCCGCCTT | 23092 |
| rs538376297 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037063 | TATTATGTTATTCCT[A/C/G]TACTGTTATTGGGAA | 23092 |
| rs538393801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111386 | CAGACTGCAGACTTT[C/T]TGGTCTCAAATTCTA | 23092 |
| rs538396869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088145 | TCAAAAGTTCCCCAT[C/T]TTATGTGCTTCTGAG | 23092 |
| rs538399871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974168 | GGTCATTCCGTTGCT[A/C]TCCTGTTCCATTTAT | 23092 |
| rs538399954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982146 | CTGATGGTTTGATCT[A/G]AGTCCGTTTCCTGCC | 23092 |
| rs538408149 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823945 | ACTGAAAAGATCTTT[A/T]CTTTCAGTGGTTTAT | 23092 |
| rs538414566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024381 | CTGCCATGGCCTAAT[A/T]TTCCCCTTTCCCTCA | 23092 |
| rs538414607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016972 | TCTACCACAGGTGGC[A/G]CTAATGCTCTGGGTC | 23092 |
| rs538415134 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211959 | AATCTTGGGCACCTG[A/G]ACCACTCCCTTTTAT | 23092 |
| rs538423072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143069970 | CTGGGCTCCCTTCAC[A/G]GCATGTCTTCAGATG | 23092 |
| rs538426807 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153681 | CTGCAATGATGGAAC[C/G]CAACCTTGGAGTTCT | 23092 |
| rs538437494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013518 | TTCAAATTTCTAGAA[A/G]TATGTAGAGTAAAAA | 23092 |
| rs538445056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920951 | TCATTCCCTCCCTCC[C/T]TCCTTCCTTATTTTA | 23092 |
| rs538447087 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143009939 | CTCCTGGAGAGTTGA[A/G]TTCTATTGTATTAAG | 23092 |
| rs538450237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937980 | TTAGTTATATGAAAC[C/T]ATATTAAAGTAGTTA | 23092 |
| rs538450270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143010756 | GAAACCTTGAAAGAG[A/G]GTAATTTGGCACAAA | 23092 |
| rs538452451 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067102 | GATGCAGCTGTCTTT[A/G]CTAGAGTTTAATAAC | 23092 |
| rs538481741 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996032 | AACATAACATACCGG[G/T]GCCTACTGGGGGGTG | 23092 |
| rs538486789 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065799 | AATGGCATTCACACA[C/T]GGATACGCTGGGACA | 23092 |
| rs538492727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058854 | ATTGGGAAGGAATTC[A/G]GCAAAGCCACAGTTG | 23092 |
| rs538502903 | in-del | -/CTTTT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993842 | CTTTTCTTTTCTTTT[-/CTTTT]TTTAAGTAGAGGCTA | 23092 |
| rs538503999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790593 | TTCGGACACCTTACC[A/G]TGGTTCATGCGGCCT | 23092 |
| rs538505043 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849538 | TTCTGAACGTCCCTT[C/T]CTTGCTCACCTTCTT | 23092 |
| rs538515394 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822359 | TTAATCTCGAAAGGG[A/G]AAGGCTATCTTCATT | 23092 |
| rs538533251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209164 | TCAAGAGAGTGAAAT[C/T]ACTCAGCTAAAATCC | 23092 |
| rs538536575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798660 | GTATGTAGCGAGAAG[A/G]GGAAGAGCAAAGAGT | 23092 |
| rs538537865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937292 | TATGGCGAATAAGCA[C/T]AGGAAAAGATGTTCA | 23092 |
| rs538544928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203305 | CATTTATGTGGCAAA[C/G]AAACATATAAAAAAA | 23092 |
| rs538545612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121455 | GTTATTTTATCCTCA[A/C]AACAATTCAATGAAG | 23092 |
| rs538548268 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142936824 | TAAACATCCATAGGA[-/A]AAAAAAAAAAAAGCC | 23092 |
| rs538548504 | in-del | -/TT | 0.0197882 | 0.097481 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992440 | TTATTTTATTTTTTA[-/TT]TTTTTTTTTTTGAGA | 23092 |
| rs538557747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121944 | CTTAAATAAAAACTT[G/T]GCCTAGAATGGCAAA | 23092 |
| rs538582194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037919 | GAAAAGGGGTCAGGC[C/T]CATGTTCACACTGAT | 23092 |
| rs538589525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142892142 | AAAGGAAGTATTTGG[A/G]ACTTCTGTGAACATG | 23092 |
| rs538602825 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991117 | GGGCTCCACCCAGTT[C/T]GAGCTTCCTGGCCGC | 23092 |
| rs538609174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113693 | AGAGGAAGAAACAGT[A/G]TTTAGTCCAGTATCA | 23092 |
| rs538612083 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833525 | TATTTTAAAGAATAT[-/G]ATGGACATTTTTGTA | 23092 |
| rs538618081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143198515 | CAATAGAAGCATTCT[G/T]CCCATTTAACCTTTC | 23092 |
| rs538626475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142853136 | GAAGTGGGTTTCTGG[A/G]GTGATTGGTGAGAAC | 23092 |
| rs538631501 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121574 | TTAGGGATATTAAAC[-/T]TTTCTTCATTTGTGT | 23092 |
| rs538634870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173485 | TCCAAGATGTTTCTC[C/T]AAAAACGAAGTGGCT | 23092 |
| rs538650130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142844765 | GAGGCGGAGGCAAGA[G/T]AATCGCTTGAATCTG | 23092 |
| rs538654973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143193681 | AGTGAAAAGGTGAAA[A/G]TTACTGACTTAAGGA | 23092 |
| rs538658828 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142836727 | TAAATAAGACTTTAT[A/G]GTTCATGTTGTTATT | 23092 |
| rs538661349 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934193 | CCCCACCACTTAGAT[A/G]TTTGTTCTCTGTCTG | 23092 |
| rs538675268 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852567 | ATGCCTATGGCTTGT[A/G]ACAGTCGGGATTTCT | 23092 |
| rs538681510 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164841 | CCTTGGCACACCTCA[A/G]GAAGAATTAGGTCTC | 23092 |
| rs538696860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143080971 | TATTTTTAAAGATAA[C/G]GCCAACAGGATTAAC | 23092 |
| rs538697731 | snp | C/T | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961589 | AGTTTAAGGGAAATA[C/T]CAGCCTGTCACCTGA | 23092 |