| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs23282 | snp | C/T | 0.468349 | 0.121752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890736 | AACTGGAAAGTGTCC[C/T]GTGCATGTCGGTGGT | 23092 |
| rs26690 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904475 | CTGGAGTACAGTGGT[A/G]GCAATCTCAGCTCAC | 23092 |
| rs26691 | snp | C/T | 0.446249 | 0.154875 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904177 | AAGTGAGCCTTTGTT[C/T]CTACTTTTCATAAAA | 23092 |
| rs26692 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903003 | GTATTCAGGGCGACT[G/T]TGAAGGATCATCCCA | 23092 |
| rs26693 | snp | C/T | 0.468949 | 0.12067 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900701 | CTTACTAAACATAAT[C/T]CCATCCCACTTATTT | 23092 |
| rs26696 | snp | A/T | 0.455383 | 0.142541 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142885037 | CCAAGATTCCCCCTC[A/T]AAGAACTTTGTGAAA | 23092 |
| rs26697 | snp | A/C | 0.438526 | 0.164189 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142944847 | AGAACACAAGCGAAA[A/C]TTAGGTTTGTACCTT | 23092 |
| rs26698 | snp | A/G | 0.440884 | 0.161442 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945989 | ATCTGGACATCAGCT[A/G]GTGGTGATGTTCCTT | 23092 |
| rs26699 | snp | C/T | 0.437401 | 0.165472 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946278 | CCAACAACTACAATA[C/T]AGATAACAAACTGTA | 23092 |
| rs26706 | snp | C/G | 0.4582 | 0.138394 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877295 | CAGGAAGTCAGGAAA[C/G]GCTTCCCAGAGAAGG | 23092 |
| rs26707 | snp | C/G | 0.489893 | 0.0703642 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874108 | GGCGGGGACCTCCCT[C/G]TCCACAGCACAGGAG | 23092 |
| rs27131 | snp | A/G | 0.21725 | 0.247846 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142945927 | AAATGAGACTGAGGA[A/G]ATGTGACAACTAATT | 23092 |
| rs27546 | snp | A/T | 0.477345 | 0.103991 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886180 | AACATATGACAGAGG[A/T]CAAGCAAACTGTTGA | 23092 |
| rs27779 | snp | G/T | 0.475259 | 0.108435 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879518 | ATTTCTGAAGACTTT[G/T]TTTTAAAGAAAGGTG | 23092 |
| rs27899 | snp | C/G | 0.483923 | 0.0882034 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142904030 | CCAAAGGATACACTG[C/G]TGATAGATAACAGGG | 23092 |
| rs27958 | snp | C/T | 0.487241 | 0.0788465 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142874121 | AGGAAACAGGAGTGG[C/T]GGGGACCTCCCTGTC | 23092 |
| rs28052 | snp | C/G | 0.472052 | 0.11486 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900305 | AGTGGTAAGCCCCAT[C/G]GAGTCACTAGAGACT | 23092 |
| rs28053 | snp | A/C | 0.214541 | 0.247473 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142946674 | AAACAACCTAATTTG[A/C]AGACTTTCTAATACT | 23092 |
| rs28304 | snp | A/G | 0.442655 | 0.159323 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142902294 | GCTACAGACGCTACA[A/G]ATTTGAAACATAACC | 23092 |
| rs35290 | snp | C/T | 0.496968 | 0.0388195 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142970658 | GATGGCTCCCCTGTC[C/T]GTTACACCCTGGCCA | 23092 |
| rs35291 | snp | A/G | 0.497558 | 0.0348586 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969500 | ATAAAATCAAGCTTT[A/G]TTTGTTTAAATCTGG | 23092 |
| rs35292 | snp | C/T | 0.0383493 | 0.133136 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903490 | ACAAAGTATCTGTTT[C/T]AACAATCCAGATCAA | 23092 |
| rs35293 | snp | C/T | 0.325799 | 0.238232 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142849036 | TCACCATGGAACCAA[C/T]AAACAACATGGAAGA | 23092 |
| rs35294 | snp | G/T | 0.457037 | 0.140127 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979472 | TTGAGTCAAAAGGAA[G/T]ATGTCCCATAGTCTC | 23092 |
| rs35295 | snp | A/C | 0.497359 | 0.0362457 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977551 | CAAAGATCCGTATCC[A/C]GCAGGGGGAAAAAAA | 23092 |
| rs35296 | snp | A/T | 0.486984 | 0.079614 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142835841 | TCTAATTGAGATCAC[A/T]GTAAGAGCTAAATTA | 23092 |
| rs35297 | snp | A/G | 0.356597 | 0.226135 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142837505 | TGAGCTTCACTTGGC[A/G]ATGATAAGAAGGCCT | 23092 |
| rs35298 | snp | C/T | 0.361263 | 0.223876 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841643 | GCTCCCTTGCACTCA[C/T]GGGACAAGCTTTCAG | 23092 |
| rs35299 | snp | C/T | 0.425894 | 0.177655 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823211 | CTCATGTGTTTAGCA[C/T]GAGCTTCCATGCCAG | 23092 |
| rs35300 | snp | A/G | 0.29789 | 0.24537 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823490 | GTCACACAGTCCCAA[A/G]AGCCAGGCTTTAGGG | 23092 |
| rs35301 | snp | C/T | 0.29789 | 0.24537 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823642 | ACCCTTGGTCCTACA[C/T]CTTGAGGAAGGAAAC | 23092 |
| rs35302 | snp | A/G | 0.474272 | 0.110462 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824508 | TCTGGCTCTCTTGCC[A/G]GGACACCCACTCTGG | 23092 |
| rs35303 | snp | C/T | 0.474363 | 0.110278 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142824985 | ACCAATGAAAATGGA[C/T]CAGCAACTCTTTTCA | 23092 |
| rs35314 | snp | A/G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877620 | TATGGCTGGGCGAAG[A/G/T]ACTTGGGGGTCCTGA | 23092 |
| rs37184 | snp | A/G | 0.41441 | 0.188333 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932405 | GAGGTAAGTTACTAC[A/G]GGAGGCTGAACCAGA | 23092 |
| rs37185 | snp | A/G | 0.499831 | 0.00918375 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931334 | CACAAATGGTACTCC[A/G]CAAGAAAAAGAGACT | 23092 |
| rs37186 | snp | A/G | 0.581317 | 0.151092 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930327 | TGCCAGACTCAGTGG[A/G]TATCTGCAGACTGCT | 23092 |
| rs37187 | snp | C/G | 0.472989 | 0.113031 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928625 | GCTGGCAAGATAATA[C/G]AGCCAGGATGTGAAC | 23092 |
| rs37188 | snp | A/C | 0.427727 | 0.175821 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928233 | TAAAAAAAAAAAAAA[A/C]ACACACACacacaaa | 23092 |
| rs37189 | snp | A/G | 0.234109 | 0.249494 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142924620 | TGAGAGACAGAGGAA[A/G]TAAGAAACCAGAAGA | 23092 |
| rs37190 | snp | A/C | 0.209997 | 0.246779 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923927 | ttgcagtgagcggag[A/C]ttgcgccactgcact | 23092 |
| rs37191 | snp | A/G | 0.22263 | 0.248497 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142920928 | GGGAATGAATTCAGC[A/G]TATTCCAGTCATGCC | 23092 |
| rs37192 | snp | C/T | 0.419135 | 0.184101 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918578 | AAATCATGTAGAAGC[C/T]AATACAAAAGGGTGT | 23092 |
| rs37193 | snp | A/G | 0.204803 | 0.245881 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142979182 | TCCTATCTTCTTTAA[A/G]CTAATAACGTTTTTT | 23092 |
| rs37194 | snp | A/C | 0.244776 | 0.249945 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978337 | GCCAAGGATTTCTCA[A/C]ACATTATCTCATACC | 23092 |
| rs37195 | snp | C/T | 0.204803 | 0.245881 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978193 | AGGCCTTGGGCAAAC[C/T]CTAAGCCCCTCTGAA | 23092 |
| rs37196 | snp | A/G | 0.20511 | 0.245937 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142977412 | TTTTTTTTTAATAAG[A/G]TTAATTGATGGCCCT | 23092 |
| rs37197 | snp | C/G | 0.20511 | 0.245937 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142975503 | AAGAAACAATAACCA[C/G]ATTCAGGTCATTTAA | 23092 |
| rs37198 | snp | A/C | 0.21695 | 0.247806 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973843 | TCCCACCCACCTCCC[A/C]CTAAACCAACGGAGA | 23092 |
| rs37199 | snp | G/T | 0.301681 | 0.2446 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973532 | ACTATACAGAAAAGT[G/T]TAAAAATGGAAGGTT | 23092 |
| rs37200 | snp | A/G | 0.221737 | 0.248397 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971111 | ATCATTATAATGGAC[A/G]TCTCTGAAAAAAAAT | 23092 |
| rs37201 | snp | A/C | 0.216649 | 0.247765 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969171 | GGCAGATTGCTTGAG[A/C]ACAGGAGTTCAAGAC | 23092 |
| rs37202 | snp | A/C | 0.222928 | 0.24853 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965939 | AAGATTAAACTAAAA[A/C]TTTTTACAGGCCCTT | 23092 |
| rs37203 | snp | A/G | 0.218151 | 0.247963 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964735 | ATTTCGGGTGATCCA[A/G]AAATGCATGTCAGGT | 23092 |
| rs37204 | snp | C/T | 0.216649 | 0.247765 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963509 | aaaaaataagagatg[C/T]tggtaaggttgtgga | 23092 |
| rs37205 | snp | C/T | 0.431621 | 0.171796 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962560 | AACAAGGAAAATTCT[C/T]GTGGATTTCTGGTTG | 23092 |
| rs37206 | snp | A/C | 0.440609 | 0.161766 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961210 | AGCCACCGTGCCCAG[A/C]GTGGATCCATTTTTT | 23092 |
| rs37207 | snp | A/G | 0.223225 | 0.248562 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960629 | TTTCTTTCACATTAc[A/G]gtagtctcccctcat | 23092 |
| rs37208 | snp | C/G | 0.182933 | 0.240836 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958768 | GTTGAATTTGCTAAT[C/G]ACACTCATTTTTCCC | 23092 |
| rs37209 | snp | A/C | 0.27008 | 0.249192 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958748 | TCATTTTTCCCAGCT[A/C]ATTAGCATACCTGTA | 23092 |
| rs37210 | snp | C/T | 0.417521 | 0.185571 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956623 | CACAGATGTCTTGAA[C/T]GATTTACAATTTCTG | 23092 |
| rs37211 | snp | A/C | 0.416218 | 0.186739 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955601 | CTACAATGATTGAGG[A/C]GGGAGGTTTGTGATA | 23092 |
| rs37212 | snp | A/G | 0.430285 | 0.173197 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953438 | AAGACTTTTTGCATG[A/G]AAGTTTTAAAAATGA | 23092 |
| rs37213 | snp | G/T | 0.415563 | 0.18732 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953310 | GGTGACCAATCTGTT[G/T]GCTTGTTGACTCTCT | 23092 |
| rs37214 | snp | A/G | 0.361263 | 0.223876 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899071 | TGAGGATGAAGGACT[A/G]GAGGGAGGCATCTAT | 23092 |
| rs37215 | snp | A/T | 0.230017 | 0.2492 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894893 | CATCATGGTCCACTC[A/T]GCAGAGTCTCTATGC | 23092 |
| rs37216 | snp | C/T | 0.110029 | 0.207142 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894382 | TGAGGGATGAATATA[C/T]GGGTACATCATTAAA | 23092 |
| rs37221 | snp | C/G | 0.428333 | 0.175206 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939212 | AAAAATAGCACAGAA[C/G]TGGAAGCTAAGAGAC | 23092 |
| rs37222 | snp | A/T | 0.473266 | 0.112482 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142938090 | ttaactagactatac[A/T]cgttgttcaaactcc | 23092 |
| rs37223 | snp | C/T | 0.447809 | 0.152878 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937659 | tgtttaaccattcac[C/T]cattaaaggacatct | 23092 |
| rs37224 | snp | C/T | 0.430732 | 0.172731 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935706 | GATGACCTTCTGCCA[C/T]CATTTATACagctcc | 23092 |
| rs40127 | snp | A/G | 0.32768 | 0.237625 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142850686 | AATAGAGGACCTACT[A/G]TGTGTCTGACATTGA | 23092 |
| rs40128 | snp | A/G | 0.417521 | 0.185571 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142826017 | GTTAACCAGCAAATC[A/G]ATAAGAAAATCTAGG | 23092 |
| rs40193 | snp | A/C | 0.223225 | 0.248562 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967138 | CACTAAAAGAACATT[A/C]AGAATAACACCTTAA | 23092 |
| rs40360 | snp | C/T | 0.215747 | 0.247642 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956044 | CATTACACAATATGG[C/T]TTTGAATATTCTCAG | 23092 |
| rs42464 | snp | C/T | 0.419296 | 0.183954 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142952069 | GAGACAGAAGAGCAG[C/T]GAAAGAGAAGTGGTC | 23092 |
| rs42465 | snp | C/G | 0.213333 | 0.247296 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937052 | taccagggtctttca[C/G]acacaaagcaaaagc | 23092 |
| rs42466 | snp | C/T | 0.418653 | 0.184544 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934665 | AATAAGGCAACGACA[C/T]TAACACCGACTAGAG | 23092 |
| rs42866 | snp | A/T | 0.438386 | 0.164349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142852691 | CTTCCCATTGTCTCC[A/T]TCCAAGACACTCGAC | 23092 |
| rs43158 | snp | A/G | 0.219349 | 0.248114 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971509 | TTGCTCAAACTTCCT[A/G]CAGCGCTGCTAATTA | 23092 |
| rs114534 | snp | A/G | 0.476487 | 0.105846 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154092 | attcattccacaaat[A/G]tcaattgaactccta | 23092 |
| rs114539 | snp | C/T | 0.40733 | 0.194287 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119238 | CAATATAAAAATACA[C/T]GGTTTGGATGATGAT | 23092 |
| rs121882 | snp | A/G | 0.471292 | 0.116318 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153779 | CGTGTGTGTTAAGAC[A/G]GAAGGACGAGAAAAA | 23092 |
| rs121883 | snp | A/G | 0.476918 | 0.104919 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153164 | TAGAATCTCAGTTAC[A/G]AGTTGTTTTCTTTCC | 23092 |
| rs151972 | snp | A/C | 0.421051 | 0.182323 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996417 | caacctccacctccc[A/C]ggttcaagcaattct | 23092 |
| rs151973 | snp | A/T | 0.448066 | 0.152544 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993975 | ATCTTAGATTCAGTT[A/T]ACATTAACTTCAAAA | 23092 |
| rs151974 | snp | A/G | 0.419135 | 0.184101 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991245 | ctcagagggtcccac[A/G]cccacggagccttgc | 23092 |
| rs151975 | snp | C/T | 0.38286 | 0.211774 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990247 | acaagcttcagtagc[C/T]gatttgatcaagtgg | 23092 |
| rs153163 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953174 | GTCAAGAATGAGAGC[A/G]GTAGTGGGAATCCAG | 23092 |
| rs153164 | snp | A/G | 0.433673 | 0.1696 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142937363 | aattttagtcattct[A/G]gaaggtgatagttca | 23092 |
| rs153165 | snp | C/T | 0.434831 | 0.168337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922100 | TGAAGCATGTATCAA[C/T]AACAGGTTATCACAT | 23092 |
| rs153166 | snp | C/T | 0.423726 | 0.179776 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923052 | ACATGAATTCTAAGA[C/T]TCCAAGAACTTCTCC | 23092 |
| rs153167 | snp | C/G | 0.43555 | 0.167544 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913637 | CAATCATGCTAAATA[C/G]TTTTCTTTAAAAGTC | 23092 |
| rs153168 | snp | A/C | 0.447809 | 0.152878 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896181 | ATGTGACAGCATTTG[A/C]ATTCCTGCCCTGACC | 23092 |
| rs153169 | snp | A/C | 0.454664 | 0.143571 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897567 | TTACTAAACTACAGG[A/C]TACTGGGCCCCTCCC | 23092 |
| rs153170 | snp | C/T | 0.44768 | 0.153045 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897686 | GCTTAGCACGGTACA[C/T]GACAGTTTCAGATAA | 23092 |
| rs153171 | snp | C/T | 0.478768 | 0.100824 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898154 | GTGTGTATATATATA[C/T]ACACACATATATATC | 23092 |
| rs153172 | snp | G/T | 0.473359 | 0.112298 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898453 | GAAATATTCAGGATG[G/T]AAAACTCGGAGGATG | 23092 |
| rs154786 | snp | C/T | 0.406814 | 0.194704 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143227406 | AGTCAGCAGGATGTC[C/T]TCTCACCCACCCTGT | 23092 |
| rs154787 | snp | A/C | 0.456332 | 0.141164 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226736 | TCTTATGTCAGACCA[A/C]ACTGTCTTTTTGAAT | 23092 |
| rs165964 | snp | C/T | 0.29789 | 0.24537 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985681 | aggaacatcacacac[C/T]agggcctgttgtagg | 23092 |
| rs165985 | snp | A/G | 0.203575 | 0.245652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124215 | CCTAATGATTATTCC[A/G]AAGCACAAAGTAAAT | 23092 |
| rs166155 | snp | C/G | 0.498059 | 0.0310896 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964807 | tcgtcgccgcacaca[C/G]ggagaagcccaccga | 23092 |
| rs168667 | snp | C/T | 0.202035 | 0.245356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000950 | ttaaaatctagatga[C/T]gggtggataggtgca | 23092 |
| rs168668 | snp | A/G | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009309 | gatgacaatgacgac[A/G]atgatgatgctgacg | 23092 |
| rs171538 | snp | A/G | 0.336702 | 0.234484 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143026578 | tcctgatattcctag[A/G]acacaagtagctcac | 23092 |
| rs171540 | snp | A/G | 0.203267 | 0.245593 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012949 | AGAAAAAAATCggcc[A/G]ggcacagtggctcat | 23092 |
| rs171812 | snp | C/T | 0.351418 | 0.228505 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160083 | gacagagcgagactc[C/T]gtctcaaaaaaaaaa | 23092 |
| rs173468 | snp | C/T | 0.203575 | 0.245652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001009 | tgtaacaaacctgca[C/T]gttctgcacatgtat | 23092 |
| rs173497 | snp | C/T | 0.415563 | 0.18732 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123495 | CTCTGGATTTGATGG[C/T]TAAAGTTAAGTTCTA | 23092 |
| rs173499 | snp | A/G | 0.460477 | 0.134905 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143032770 | GCTGATTAGATTACT[A/G]ATAATTAACAACGGT | 23092 |
| rs173740 | snp | C/T | 0.497829 | 0.0328757 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965055 | tctctgccttggctg[C/T]caggcagggaagggc | 23092 |
| rs173750 | snp | A/G | 0.498009 | 0.0314867 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964745 | GCAAGAGATAATTTC[A/G]GGTGATCCAGAAATG | 23092 |
| rs174049 | snp | A/G | 0.475965 | 0.106957 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154420 | TACTAAAATACGTAA[A/G]TAAAAGATGATCTTA | 23092 |
| rs181771 | snp | C/T | 0.423881 | 0.179625 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143125839 | CAGAGCTAAAAATAT[C/T]AATTTTATAGGGTTG | 23092 |
| rs181865 | snp | A/G | 0.441705 | 0.160466 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949401 | GGTTAGAGAGATGAC[A/G]GTGGCAAAAATGAAG | 23092 |
| rs181867 | snp | C/T | 0.479095 | 0.100076 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831332 | GTTATTCTGATTTTC[C/T]CCCACCCCCTGGCCT | 23092 |
| rs183636 | snp | C/G | 0.373598 | 0.21731 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049717 | AAATTATGTACAATA[C/G]CCCTCCAATCATCAG | 23092 |
| rs183692 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878429 | TCAAACATATTTGAA[C/T]GACTAAATGAATGAA | 23092 |
| rs185023 | snp | G/T | 0.428333 | 0.175206 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143123397 | TAGAATTGCTGTGAG[G/T]TGAACACCACAGACT | 23092 |
| rs185200 | snp | C/T | 0.494333 | 0.0529293 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142875114 | AAACTCCTGCAAAGA[C/T]CTTGCTGGAAAACAG | 23092 |
| rs185205 | snp | A/G | 0.292266 | 0.246401 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794514 | AACCACAGCCTGATC[A/G]CCCAAAGTAATTTTC | 23092 |
| rs185207 | snp | C/T | 0.484701 | 0.0861117 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848461 | AAAACAAGGAAGAAC[C/T]GGAAGGGAGTAAAGG | 23092 |
| rs187395 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998195 | tacaatcataaatat[A/T]aatatgaaatctata | 23092 |
| rs187396 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142978364 | TAGACAGAGCCCCTC[A/T]CTCCAAAGATGGCCA | 23092 |
| rs187418 | snp | G/T | 0.232359 | 0.249377 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124008 | GACTAGACAGAAGAA[G/T]AGTCACCCCTAGACA | 23092 |
| rs187419 | snp | C/T | 0.316968 | 0.240864 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031357 | CCTCCTGGCTGGTCT[C/T]CTTATTCTTCTTGTT | 23092 |
| rs187552 | snp | C/T | 0.313326 | 0.241847 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880017 | TATATTTTAAAATTA[C/T]TTGCCAACAAGAAAT | 23092 |
| rs187729 | snp | C/T | 0.41833 | 0.184838 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226004 | CAGGAAACTTTAGGG[C/T]AGATGAGGAGAATGA | 23092 |
| rs190313 | snp | C/T | 0.427727 | 0.175821 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040507 | TCCTGTTCACCATTA[C/T]ATCCTCAGTCCCTGG | 23092 |
| rs192183 | snp | G/T | 0.487432 | 0.0782705 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023525 | CAGAAAAGAGGATTT[G/T]TTTTTCTTTTGCTTC | 23092 |
| rs192194 | snp | C/T | 0.414217 | 0.188501 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037176 | CTAGCAACTTGACTG[C/T]CCTTCTCTTGCTCTT | 23092 |
| rs194490 | snp | C/T | 0.347032 | 0.230401 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156040 | ATAGGCTTAAGATTT[C/T]GCATGGCTTTTTCAA | 23092 |
| rs244468 | snp | C/T | 0.492386 | 0.0612297 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143224856 | CATGACAAACCCCTG[C/T]TAACTTTAAAACCAC | 23092 |
| rs245710 | snp | C/T | 0.346147 | 0.230772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887794 | TATTTTTAGTAGAGA[C/T]GAGGTCTCACCATGT | 23092 |
| rs245711 | snp | A/T | 0.414905 | 0.187899 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142933556 | TAGCAGAATGACCCT[A/T]CTAGGCATGGACTCC | 23092 |
| rs245712 | snp | C/T | 0.20511 | 0.245937 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997951 | cttattcaatttctg[C/T]tgctgaattgttttc | 23092 |
| rs245713 | snp | C/T | 0.185788 | 0.241613 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997847 | ccacaaggcacatca[C/T]aaacttctttcactt | 23092 |
| rs245714 | snp | A/G | 0.459914 | 0.13578 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142996319 | atttttagtagagac[A/G]gagtttcaccatgtt | 23092 |
| rs245715 | snp | A/G | 0.458545 | 0.137872 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142993359 | acaaggtgaaacccc[A/G]tctctactaaaaata | 23092 |
| rs245716 | snp | A/C | 0.188631 | 0.242351 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991264 | gattatatcctgcac[A/C]tggctcagagggtcc | 23092 |
| rs245717 | snp | C/G | 0.448066 | 0.152544 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990854 | ggccgactgacaact[C/G]atacagccagatgcc | 23092 |
| rs245718 | snp | C/T | 0.45843 | 0.138046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990711 | ggacctccagcgaac[C/T]ccaacagacctgcag | 23092 |
| rs245719 | snp | G/T | 0.45843 | 0.138046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142990429 | tgagatgatcggtaa[G/T]aataaacttctctga | 23092 |
| rs245720 | snp | A/C/T | 0.046775 | 0.145601 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142989169 | cccaatacaggagca[A/C/T]ccagattcataaagc | 23092 |
| rs245721 | snp | A/C | 0.448066 | 0.152544 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988420 | ttttgaaaagatcaa[A/C]aaacttgatagacca | 23092 |
| rs245722 | snp | A/C | 0.448195 | 0.152377 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988360 | gaagaataaactaga[A/C]acaataaaaaatgat | 23092 |
| rs245723 | snp | A/T | 0.419135 | 0.184101 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987993 | atgaggccagcatca[A/T]cctgataccaaagcc | 23092 |
| rs245724 | snp | A/G | 0.445064 | 0.156365 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987738 | attatctcaatagat[A/G]cagaaaaagcctttg | 23092 |
| rs245725 | snp | A/G | 0.445064 | 0.156365 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987730 | aatagatgcagaaaa[A/G]gcctttgacaaaatt | 23092 |
| rs245726 | snp | C/G | 0.447809 | 0.152878 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986159 | aaacaacaggtgctg[C/G]agaggatgtggagaa | 23092 |
| rs245727 | snp | A/G | 0.440471 | 0.161928 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985955 | acgtatgtttattgc[A/G]gcactattcacaata | 23092 |
| rs245728 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985420 | aatgagtgattagtg[A/G]gtgaacatgaaggcc | 23092 |
| rs245729 | snp | A/G | 0.298398 | 0.245271 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983612 | TCGATGTAAAAATGC[A/G]TGAAAATCTGCATTC | 23092 |
| rs245730 | snp | A/G | 0.189261 | 0.242509 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142983384 | AACCTGTCTCTACTA[A/G]TAATACAAAATTAGC | 23092 |
| rs245731 | snp | A/G | 0.298398 | 0.245271 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142981793 | TGTGGTGGTACCACG[A/G]CACCACTTAGGGACA | 23092 |
| rs245779 | snp | A/T | 0.415891 | 0.18703 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142940785 | ctggccaaattcttt[A/T]accataaagacatat | 23092 |
| rs245780 | snp | A/G | 0.280785 | 0.248097 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142951948 | TCTTCCCTGGAGGGA[A/G]CATGGCCCTGCCAAC | 23092 |
| rs245813 | snp | A/T | 0.382473 | 0.212016 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017460 | AACAGGGGAGTGTGA[A/T]GAATTCATCTCTCTA | 23092 |
| rs245814 | snp | G/T | 0.198324 | 0.244601 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017891 | tatgcatagcctttg[G/T]ccagcaatgctttgg | 23092 |
| rs245815 | snp | A/C | 0.316453 | 0.241006 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018376 | ttgaaaatcataaac[A/C]agaaagcaaaaaaga | 23092 |
| rs245816 | snp | A/G | 0.385932 | 0.209815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018880 | aatgcactcgcaaag[A/G]aaaattttattttag | 23092 |
| rs245817 | snp | C/T | 0.388775 | 0.207946 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020732 | AGAATGGCGTGAACC[C/T]GGGAGGGGGAGCTTG | 23092 |
| rs245818 | snp | C/T | 0.394538 | 0.203982 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021382 | ACCTGGAAAGAGCAT[C/T]AGTCTAACAATGATA | 23092 |
| rs245819 | snp | C/T | 0.397633 | 0.201754 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143021410 | TAGGCCAATGTTATT[C/T]GTAATACCAAAAACC | 23092 |
| rs245820 | snp | C/T | 0.334182 | 0.235401 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022645 | AACCTCATGCCATCC[C/T]ATTTAGACTAATTTT | 23092 |
| rs245821 | snp | C/T | 0.179425 | 0.239831 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023632 | GCAGCCTCTGGATGG[C/T]TCTGATCCCAAAAGG | 23092 |
| rs245822 | snp | A/G | 0.258843 | 0.249844 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038884 | acatggtgaaacccc[A/G]tctctattaaaaata | 23092 |
| rs245823 | snp | C/T | 0.148326 | 0.228391 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038760 | TGCAGTGAACCGAGA[C/T]TGCATTACTGCACTC | 23092 |
| rs245824 | snp | A/T | 0.49995 | 0.00499176 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038376 | AATAACTGAACATTT[A/T]AAAAAATGTTTCCAT | 23092 |
| rs245825 | snp | A/G | 0.139564 | 0.224285 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143038258 | CTCACAGTCCTTATG[A/G]AAAAAAAAGTGTATA | 23092 |
| rs245826 | snp | C/G | 0.243347 | 0.249911 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036509 | AGAGGAAAATTAAAA[C/G]AGCCAAGAACAAAGA | 23092 |
| rs245827 | snp | A/G | 0.499965 | 0.00419314 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035116 | ACTTATTGCTTAGTG[A/G]TGCTTATTACAAACA | 23092 |
| rs245828 | snp | C/T | 0.493477 | 0.0567349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034581 | ccatgtcttcccttc[C/T]cccagctgtgggaag | 23092 |
| rs245829 | snp | A/T | 0.490782 | 0.0672626 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034213 | gggtcacagaatgac[A/T]ccgtgcttaactttt | 23092 |
| rs245830 | snp | C/T | 0.203882 | 0.245709 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033750 | TTTTACACAGTGCTA[C/T]GGGGAGCTGCAGACA | 23092 |
| rs245831 | snp | C/T | 0.493613 | 0.0561475 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143033712 | TGAACTAGGATGTTT[C/T]AAGAGTAGGCTTGTG | 23092 |
| rs245832 | snp | A/G | 0.190519 | 0.242821 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030748 | TTTCATTTTGGATAC[A/G]TGAATAGGTAAATTA | 23092 |
| rs245833 | snp | A/G | 0.334412 | 0.235318 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029389 | AAAAAAAAAAAACTG[A/G]GAAGTAAAGGATTTC | 23092 |
| rs245845 | snp | C/T | 0.220843 | 0.248294 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000634 | aaccaattcaaatgc[C/T]catcaatgataggct | 23092 |
| rs245846 | snp | C/G | 0.204803 | 0.245881 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003968 | GGAGTCTCTCTGAAT[C/G]TGTGGTGATTCTGGG | 23092 |
| rs245847 | snp | C/G | 0.485664 | 0.0834419 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004136 | AACCACTTATACACT[C/G]ATGAGTGTTCAAACT | 23092 |
| rs245848 | snp | A/G | 0.38555 | 0.210062 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007013 | CGAACTCCTGAGCTC[A/G]GGCAATCCACCCGCC | 23092 |
| rs245849 | snp | A/G | 0.202959 | 0.245534 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143007264 | AGATTTCTCAGTTGA[A/G]CACATTAGAATGCTC | 23092 |
| rs245850 | snp | A/G | 0.202959 | 0.245534 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143011008 | ACAGTGTAATAGCTA[A/G]GACCAGCAATCCATG | 23092 |
| rs245851 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012544 | tatatatgtatgtat[A/G]tatataaatatatCC | 23092 |
| rs245852 | snp | C/T | 0.357995 | 0.225471 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143014815 | GGAAGGATTTTGTTT[C/T]TTCTCCTATACACCA | 23092 |
| rs245853 | snp | A/G | 0.195526 | 0.243993 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015385 | AGGTCTCCAGAACTC[A/G]TCTATTCTCAAGCCT | 23092 |
| rs245854 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142974891 | TATGGATGTGGAACA[A/C]GGGAGGCTAGCAAAA | 23092 |
| rs245856 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963188 | acacatatatatata[C/T]atatatatatatatc | 23092 |
| rs246595 | snp | C/T | 0.423413 | 0.180077 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143126279 | TCTTTCACAACCATG[C/T]CATTTTAATACAAAC | 23092 |
| rs246596 | snp | C/T | 0.150667 | 0.229419 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124449 | CACAAGGGGCACACA[C/T]AAGCCCTTCTCAAAT | 23092 |
| rs246597 | snp | C/T | 0.148661 | 0.22854 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124276 | TAGATGCCTAGGTTT[C/T]CACACCTTCTTTTCA | 23092 |
| rs246598 | snp | A/G | 0.23031 | 0.249223 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124144 | TAGTCGCTATGGGGG[A/G]TATATACTTTAGCCC | 23092 |
| rs246599 | snp | C/T | 0.499203 | 0.0199521 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141460 | GCCCATACGGGATAT[C/T]TGTGTGCAGATGCAA | 23092 |
| rs246600 | snp | A/G | 0.429238 | 0.174281 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137332 | TCTAGTTGAGTGGAG[A/G]AAAGGAACTTGAGTT | 23092 |
| rs246601 | snp | A/G | 0.498109 | 0.0306926 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137117 | GAGACCATTGAAGTC[A/G]TGTTCTTAGAGGTCT | 23092 |
| rs246602 | snp | A/G | 0.499801 | 0.00998203 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137105 | GTCGTGTTCTTAGAG[A/G]TCTTATGTATCAGGA | 23092 |
| rs246603 | snp | A/G | 0.457853 | 0.138915 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136970 | GGGGTTATGTACATG[A/G]CTGGCATTTGGGAAG | 23092 |
| rs246604 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136893 | TATGGAAATATATAC[C/T]TTTTTTCACAAATTA | 23092 |
| rs246605 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136874 | TTTCACAAATTATTA[C/T]ATTTGCATAATCGTT | 23092 |
| rs246606 | snp | C/T | 0.485731 | 0.0832509 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136630 | AGTCAACTCTCCCAC[C/T]GCCCCCCCACAGGGT | 23092 |
| rs246607 | snp | C/T | 0.495895 | 0.0451182 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143134121 | GCCACGCTGGCCCTA[C/T]GCAGCAAAGACTCAC | 23092 |
| rs246608 | snp | A/G | 0.288386 | 0.247035 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143132694 | TAGCTATGGTTTACT[A/G]AGTCCTTGCCACACC | 23092 |
| rs246609 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119909 | CACTGTTTCTCTGGT[A/C]CACTTTTTTTTTTTT | 23092 |
| rs246629 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060585 | GCAACCATGCACATA[G/T]TTTTGTAGTTTCAGC | 23092 |
| rs246630 | snp | C/T | 0.267364 | 0.249396 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035666 | GTAGGCCAGGTGCGG[C/T]GGCTCACGCCTGTAA | 23092 |
| rs246631 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036208 | CTGCCATTTTCTTTT[C/T]CACTCTGACCATTAA | 23092 |
| rs246632 | snp | A/G | 0.306927 | 0.243432 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143036666 | ATGTATTGGCTCTGC[A/G]TCTTTGGTCAAGATA | 23092 |
| rs246633 | snp | A/G | 0.457504 | 0.139435 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037490 | AAATATCTAAAATAC[A/G]TATGATTATAGAAAC | 23092 |
| rs246634 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037647 | tatttcaagatatcc[A/G]taataattgtaatgt | 23092 |
| rs246635 | snp | C/G | 0.305934 | 0.243663 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143037656 | ATATCCATAATAATT[C/G]TAATGTGTTATGAAA | 23092 |
| rs246636 | snp | C/T | 0.457853 | 0.138915 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143031865 | AACAACTCTAAGGTA[C/T]AATCAAATGATTTTC | 23092 |
| rs246637 | snp | A/G | 0.418169 | 0.184985 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143030618 | ACCTTTTGGTCCTCC[A/G]CTTTCTCATTTTTTT | 23092 |
| rs246639 | snp | C/G | 0.0652144 | 0.168387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084335 | TGATGAGAATCTAGA[C/G]CTCATGGCTGGGCAC | 23092 |
| rs246640 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081918 | GGTTCATGCCATTCT[C/T]CTGCCTCAGCCTCCC | 23092 |
| rs246641 | snp | A/G | 0.200182 | 0.244986 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143081866 | ccaccacgcccggct[A/G]atttttttgtatttt | 23092 |
| rs246642 | snp | A/T | 0.471863 | 0.115225 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079268 | GATGTCTGAGAAAAA[A/T]AATGTTTCATAGGCT | 23092 |
| rs246643 | snp | C/G | 0.463881 | 0.12944 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078393 | TAAAAAACCAAAATC[C/G]GAATTGAAATCCAGC | 23092 |
| rs246644 | snp | G/T | 0.442249 | 0.159814 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074516 | GTATTACTCTTCTTT[G/T]CATTTTTTTCTCAAT | 23092 |
| rs246645 | snp | A/G | 0.159292 | 0.232964 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143073486 | GCCTTTTCCATAGCA[A/G]TTACTTAATATATTA | 23092 |
| rs246646 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143072545 | attccattgtgtata[C/T]acacatgccacatat | 23092 |
| rs246647 | snp | G/T | 0.432651 | 0.170701 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070564 | gggtagtgctgtcct[G/T]ttaacaatataaatt | 23092 |
| rs246648 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143069378 | GTTACCTGGATATTT[C/T]CCACTCattcactta | 23092 |
| rs246649 | snp | C/T | 0.093777 | 0.195178 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067954 | ctggtctcgaactcc[C/T]ggcctcaagtgatct | 23092 |
| rs246650 | snp | A/T | 0.093777 | 0.195178 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067681 | CAATACACCAACAAG[A/T]CCCAACATTTTGTGT | 23092 |
| rs246651 | snp | C/G | 0.438105 | 0.164671 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051288 | AGCAGTGGTTATAAG[C/G]GGAGAACGTCTTAGA | 23092 |
| rs246652 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049992 | ACCCAGAGCTGTCAT[A/G]AGATTATAATCCAGG | 23092 |
| rs246653 | snp | G/T | 0.438386 | 0.164349 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143049411 | GTAGAAATAAAAGGA[G/T]TTAAATAAGTAAAGA | 23092 |
| rs246654 | snp | C/T | 0.42357 | 0.179927 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048063 | tcaggagtccaagac[C/T]agcctggccaacatg | 23092 |
| rs246655 | snp | C/T | 0.423726 | 0.179776 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048039 | caacatggtgaaacc[C/T]tgactctactaaaaa | 23092 |
| rs246656 | snp | A/G | 0.438946 | 0.163706 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047226 | GTCTCTGCTGCCTCA[A/G]TGGGGATGTTTACCC | 23092 |
| rs246657 | snp | C/T | 0.42357 | 0.179927 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143047040 | AATGACATGTGACAA[C/T]AGACACTCTATAGTG | 23092 |
| rs246658 | snp | C/T | 0.373799 | 0.217195 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046721 | TATATAGCTGATTTA[C/T]ATATTAAATAGTATA | 23092 |
| rs246659 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045263 | CTGTAATGTCCTCCT[A/G]GCAGAGGCAGCTGCC | 23092 |
| rs246660 | snp | A/G | 0.374 | 0.217081 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143044457 | AGCAAAGTCCTCGCT[A/G]GAGCCTTCTGCCAAC | 23092 |
| rs246661 | snp | A/G | 0.36955 | 0.219562 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043513 | TCACACAGAAACTAT[A/G]TATGAAAATTTATAG | 23092 |
| rs246662 | snp | C/G | 0.427879 | 0.175668 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043434 | AATAAATGAATGGTT[C/G]GACAAAGTGCAGTAC | 23092 |
| rs246663 | snp | A/G | 0.427727 | 0.175821 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143043325 | ttacactgattgaaa[A/G]acaatgccaatccca | 23092 |
| rs246664 | snp | A/C | 0.420255 | 0.183066 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042366 | AGGATCAGAAGATTT[A/C]TCTGGTTATATATAT | 23092 |
| rs246665 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041454 | ATTAAAATGCCAAAA[A/G]TGACATTAAAAATTC | 23092 |
| rs246666 | snp | A/T | 0.420415 | 0.182917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041398 | ATCTATTTTTACACA[A/T]AAAATGAAAATACGG | 23092 |
| rs246667 | snp | A/T | 0.427727 | 0.175821 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143040454 | TAAACAAAACACGAG[A/T]TTATACTCCATCAAG | 23092 |
| rs252221 | snp | C/T | 0.498323 | 0.0289051 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142962694 | GGTTCAGGTTACTTA[C/T]CTCACACTCAAGTAG | 23092 |
| rs252222 | snp | A/G | 0.441977 | 0.16014 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963650 | cctctctgagaaggc[A/G]caggtgacatttagg | 23092 |
| rs252223 | snp | G/T | 0.498109 | 0.0306926 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964305 | aacaaatgttacagg[G/T]atatgatcaaaactg | 23092 |
| rs252231 | snp | G/T | 0.464947 | 0.127663 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949105 | TCAATTTTTTTTTTT[G/T]GAGACGGAGTCTCAC | 23092 |
| rs252232 | snp | C/T | 0.441841 | 0.160303 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949122 | ACATTTCTGTGCTTT[C/T]TTCAATTTTTTTTTT | 23092 |
| rs252233 | snp | C/G | 0.499997 | 0.00119808 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949165 | TCTCTCTCTCTCTCT[C/G]GAAATTCAACTATAA | 23092 |
| rs252234 | snp | C/T | 0.490943 | 0.0666801 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949580 | TTTAGAACATTGTAC[C/T]GAAAAGTCTTGAGCC | 23092 |
| rs252451 | snp | A/G | 0.461923 | 0.132621 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793825 | CGAAGCAGGCAGATC[A/G]CTTGAGGCCAGGAGT | 23092 |
| rs252452 | snp | A/G | 0.449853 | 0.150196 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793022 | AGCCCCTGATGCCTA[A/G]GGGGAATACCCATGG | 23092 |
| rs252453 | snp | C/T | 0.298905 | 0.24517 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830648 | AGTCTGGTCATTTTG[C/T]CCCAGTGAAAATTGA | 23092 |
| rs252454 | snp | C/T | 0.470521 | 0.117772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142830488 | GGAAAAACAGACTGA[C/T]TGCCATAACGTACTG | 23092 |
| rs252455 | snp | A/G | 0.470424 | 0.117954 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142829730 | TGTTCACCATTACCT[A/G]CTTGACCAGGTGACA | 23092 |
| rs252463 | snp | G/T | 0.459004 | 0.137176 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833227 | CCCGGCTAATTTTTT[G/T]TTTTTTTTTTTTTAG | 23092 |
| rs252464 | snp | C/T | 0.111224 | 0.207945 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833661 | CTCACACAGAAAGAG[C/T]GCAAATATCAGCGGT | 23092 |
| rs258758 | snp | A/G | 0.326035 | 0.238157 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175093 | TTCTTTTCCCCACAT[A/G]AAAGGAGCCCAAATG | 23092 |
| rs258759 | snp | A/G | 0.31357 | 0.241783 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177028 | AAGGTCAAATGGCTT[A/G]TTCAAAGTAATGACA | 23092 |
| rs258760 | snp | A/G | 0.296109 | 0.245711 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143177523 | CAGCTATGGGTGAGC[A/G]TGCATATCAAATACA | 23092 |
| rs258761 | snp | A/G | 0.330482 | 0.236691 | intron-variant, upstream-variant-2KB | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143190628 | taaattgtgcttttg[A/G]tgttaaatctaagta | 23092 |
| rs258764 | snp | C/T | 0.347032 | 0.230401 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143196888 | acctcaaaatcaaca[C/T]ctggggtgctgttga | 23092 |
| rs258765 | snp | C/T | 0.334412 | 0.235318 | intron-variant, downstream-variant-500B | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143194498 | AGTGCAAAAAGGTTT[C/T]ATACATAAATGCTTA | 23092 |
| rs258766 | snp | C/T | 0.350546 | 0.22889 | intron-variant | ARHGAP26, ARHGAP26-IT1 | GRCh38.p7 | 5:143192945 | ggagcgcctactgCA[C/T]ATGAATGCTCTTCTT | 23092 |
| rs258767 | snp | C/T | 0.340333 | 0.233109 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180717 | tgggggtgaatgctc[C/T]gtgatagtgagttct | 23092 |
| rs258768 | snp | C/G | 0.421526 | 0.181876 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181729 | GGCATCTCCAAAGTG[C/G]GGAGCTAAAGTTCCT | 23092 |
| rs258769 | snp | A/G | 0.499793 | 0.0101816 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181767 | AAAACAAAACAAAAA[A/G]TCCTTAACATCTCAA | 23092 |
| rs258770 | snp | A/G | 0.426813 | 0.17674 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143181950 | AGCCGTGTCAGGGGA[A/G]GTCGGAGAGGTTAGT | 23092 |
| rs258771 | snp | C/T | 0.325091 | 0.238456 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182166 | GTCAACTCTTACTAC[C/T]ATTAGGGAAATAACA | 23092 |
| rs258772 | snp | C/T | 0.470618 | 0.117591 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182631 | ATTAGCTAGAGTAGA[C/T]AATAAATGATCTTGT | 23092 |
| rs258773 | snp | A/T | 0.328148 | 0.237472 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184819 | ACTGAAAAAGGGGAG[A/T]GGAGGGAAGGAACGT | 23092 |
| rs258774 | snp | A/G | 0.334182 | 0.235401 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185107 | ACAATGCAACTACTG[A/G]AAATTATATTGCTGA | 23092 |
| rs258775 | snp | A/C | 0.328148 | 0.237472 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185258 | ATATATACACAAAGA[A/C]AGGTTCTAAAATAGT | 23092 |
| rs258776 | snp | C/T | 0.395453 | 0.203331 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143185296 | GTGTTAACTGTGGTA[C/T]CTGGAGTAGGAGTAC | 23092 |
| rs258777 | snp | C/T | 0.410905 | 0.191336 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167732 | TGCTGGGTTAAGAAT[C/T]TGTCTTGCCTACCAG | 23092 |
| rs258778 | snp | C/T | 0.410905 | 0.191336 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167623 | TACCATCTCTAGGTC[C/T]TAAGGAATTGTGATA | 23092 |
| rs258779 | snp | C/T | 0.281313 | 0.248031 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167397 | CCCCCCGGGTTCAAG[C/T]GATTCTCATGTCTCA | 23092 |
| rs258780 | snp | C/T | 0.34526 | 0.23114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166688 | CCAGTCCATAGATGC[C/T]TTCCCTCAGGGCTGG | 23092 |
| rs258781 | snp | C/T | 0.383824 | 0.211166 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166604 | TGAAAGCACTGGGGC[C/T]GTCAGGGGTCATGGC | 23092 |
| rs258782 | snp | C/T | 0.344592 | 0.231414 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143166383 | TCCTCCAAGTGGCTC[C/T]ACCTCCTTATAGTTC | 23092 |
| rs258783 | snp | C/T | 0.334871 | 0.235153 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143166295 | TTCCTGCCCACACTC[C/T]CTCAGTCACCCTGAT | 23092 |
| rs258784 | snp | C/T | 0.458775 | 0.137524 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143165180 | GCTGGCCTGGTTGCA[C/T]GCTGAAGCTGTGAAA | 23092 |
| rs258785 | snp | A/C | 0.4231 | 0.180378 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163643 | GCCAACATGGTGAAA[A/C]CCCGTCTCTACTGAA | 23092 |
| rs258786 | snp | A/G | 0.426201 | 0.177351 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163556 | GGCTGAGGCAGAAGA[A/G]TCGCTTGAACCCAGG | 23092 |
| rs258787 | snp | C/T | 0.450154 | 0.149794 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163351 | GGCAGATCTAGAAAA[C/T]GAACTAGGGAAATTA | 23092 |
| rs258788 | snp | C/T | 0.426507 | 0.177046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143163099 | AAGATGAGGTCTTAC[C/T]GTGTCACCCAGGCTG | 23092 |
| rs258789 | snp | C/T | 0.353803 | 0.227431 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162448 | GACTCCACTTCTTGA[C/T]TTCTGATTTCTTGCC | 23092 |
| rs258790 | snp | A/G | 0.423257 | 0.180228 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143162412 | ATTTTCACTGTGACA[A/G]CTGAACATTTTAAGT | 23092 |
| rs258791 | snp | A/G | 0.395453 | 0.203331 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161852 | CTTTCCAATTTGCTC[A/G]AAACCCAGAATGATT | 23092 |
| rs258792 | snp | A/T | 0.360006 | 0.233077 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161580 | GACCTTTATGGAGAT[A/T]TACTAGAGTTACTCA | 23092 |
| rs258793 | snp | C/T | 0.418169 | 0.184985 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143161204 | GCCAACACGGTAAAA[C/T]CCCGTCTCTGCTAAA | 23092 |
| rs258794 | snp | A/C | 0.354235 | 0.227234 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160475 | agaaagaaaaaaaaa[A/C]CACCAAAAGCAACAA | 23092 |
| rs258795 | snp | A/G | 0.351853 | 0.228311 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160452 | AGCAACAACTTCTTG[A/G]TAAAGGCCTTACTCT | 23092 |
| rs258797 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226188 | ggccATGGCATTCTT[A/T]AGCTACGAAATTTTG | 23092 |
| rs258798 | snp | C/T | 0.426201 | 0.177351 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147803 | TTATGGAAGTGGACA[C/T]GGAGTTGGCATTGAA | 23092 |
| rs258799 | snp | G/T | 0.472052 | 0.11486 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150395 | ACAAGTCATAATGTG[G/T]TCAGAGTTCAACCAC | 23092 |
| rs258800 | snp | C/T | 0.42574 | 0.177808 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153131 | GAAGATTCTGAAAAC[C/T]GAGAGGCTAGTCTCC | 23092 |
| rs258801 | snp | A/G | 0.347253 | 0.230308 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153430 | CTGAGGGCTGCAGAA[A/G]TAAATCATTCTCTCC | 23092 |
| rs258802 | snp | G/T | 0.475702 | 0.107512 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154452 | TCCAAAATAATACTA[G/T]TAATTGCCATACACA | 23092 |
| rs258803 | snp | G/T | 0.407158 | 0.194426 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154482 | AAAAGTAAGGACAGT[G/T]TGTGGGGGGAGCCCT | 23092 |
| rs258804 | snp | G/T | 0.469116 | 0.120367 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154653 | CCTCTACAGCAGAAG[G/T]TCCTTCCTCCTCTTC | 23092 |
| rs258805 | snp | A/T | 0.494442 | 0.0524218 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154854 | CTTTTTAAAAAAAAA[A/T]ATGCTATGAATTATC | 23092 |
| rs258806 | snp | C/T | 0.34437 | 0.231505 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155574 | TGCTTGGGAAAGAAA[C/T]CCTGCTGGGTCACCA | 23092 |
| rs258807 | snp | A/C | 0.344592 | 0.231414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155638 | CCTCCTCCCATACCC[A/C]CTCTGCTGACAGGCT | 23092 |
| rs258808 | snp | C/G | 0.347253 | 0.230308 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155838 | CAATTTTTGGAAACT[C/G]TTTTAGGTTATTTAG | 23092 |
| rs258809 | snp | C/T | 0.346368 | 0.23068 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155890 | CTTAAAGCTTTGGAG[C/T]TTAATTAAAGGTATG | 23092 |
| rs258810 | snp | C/T | 0.345485 | 0.231047 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143155940 | GAATTTAGCTGCCCT[C/T]AAATGCCTTATGACA | 23092 |
| rs258811 | snp | A/T | 0.347253 | 0.230308 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156361 | AATGAAGCCTATGGT[A/T]GATCCTGCCTGGCTT | 23092 |
| rs258812 | snp | A/T | 0.345037 | 0.231231 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156599 | CACTATGGCTCTCAG[A/T]CTTGAGCATGTATCA | 23092 |
| rs258815 | snp | C/T | 0.488786 | 0.0740357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209909 | CACCTCTTTGCTATA[C/T]ACTACAGTGTACAGG | 23092 |
| rs258816 | snp | A/C | 0.473266 | 0.112482 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210849 | CTAGCAGGAGGATCC[A/C]AACTTGTTCATGCCC | 23092 |
| rs258817 | snp | C/T | 0.318656 | 0.240388 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211029 | GATTGTATTTGTAGG[C/T]TTTGGCTCTGATAAA | 23092 |
| rs258818 | snp | C/T | 0.414245 | 0.188477 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143211462 | ATCTCCCTCTACTGC[C/T]TTAGGATAGGCACAA | 23092 |
| rs258819 | snp | C/T | 0.0122893 | 0.0774185 | synonymous-codon, missense, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143214087 | CACGGTCTTCGATAA[C/T]GGTGAGTTTCTCATC | 23092 |
| rs258820 | snp | A/G | 0.465996 | 0.12588 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143214956 | TAAATCAAAATGCAC[A/G]AACAGCCAGCCCAGC | 23092 |
| rs258821 | snp | A/G | 0.386504 | 0.209444 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216430 | AGGTCAGAGGGGCAG[A/G]AACTGGGCCCTGGAG | 23092 |
| rs258822 | snp | A/G | 0.495745 | 0.0459295 | intron-variant, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143216448 | ATGTCAAGTGAGGGC[A/G]TGAGGTCAGAGGGGC | 23092 |
| rs258823 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217095 | TCTGATTGGTTTGAT[C/G]ATTTAATCTGACAAC | 23092 |
| rs258824 | snp | A/G | 0.325091 | 0.238456 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217725 | CTTGGGCGTGGCAGC[A/G]AAGATGGCTGGAGAA | 23092 |
| rs258825 | snp | C/T | 0.407845 | 0.193868 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143220729 | TTAGTGATCTGAAAT[C/T]GGCCAACTTTGGAGG | 23092 |
| rs364211 | snp | A/T | 0.413748 | 0.188909 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908753 | aaagatagctacata[A/T]caccttctatgccac | 23092 |
| rs369843 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911800 | CATAAGAGATTCTGA[C/T]TTTGCTGATGTCTAA | 23092 |
| rs371846 | snp | A/G | 0.362523 | 0.223246 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808484 | CTCACAGGTTGCTAA[A/G]CATAAACTATGGCAA | 23092 |
| rs373749 | snp | G/T | 0.444533 | 0.157025 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899964 | TTTATCCTTCACTCA[G/T]AGTAAACAGAGCCTC | 23092 |
| rs374384 | snp | A/G | 0.124837 | 0.216412 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795367 | TCTTCCCTAGAGCAT[A/G]CTGTGCGGTGGTAAA | 23092 |
| rs375782 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794938 | TCTAATCCATTATAC[A/G]AGACATCAACAGATT | 23092 |
| rs377269 | snp | C/T | 0.477175 | 0.104362 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909219 | AAATTATTCAGAATA[C/T]AGTCCAGAGACTCAA | 23092 |
| rs379072 | snp | A/G | 0.381891 | 0.212379 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808194 | AGGCTGGAGTGCAGT[A/G]GTGTGATCTCAGCTC | 23092 |
| rs380551 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799387 | cgtcttgacaagcat[C/T]tgtagaatggctact | 23092 |
| rs381489 | snp | A/G | 0.395818 | 0.203069 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822542 | ACACCATGTGTGTGT[A/G]TTTGTGTATGTATCT | 23092 |
| rs381874 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142911926 | TAGGAGGAGACAGTT[A/T]ATATTCACAGGCCTT | 23092 |
| rs382344 | snp | C/T | 0.476746 | 0.10529 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908093 | TTATTCAATAATTTT[C/T]AGCATATAAAAATAT | 23092 |
| rs383898 | snp | A/C | 0.201727 | 0.245295 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142812255 | GTCTAATACAGAGGT[A/C]TTTTTTCATATTTTT | 23092 |
| rs384521 | snp | C/T | 0.467234 | 0.12373 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795211 | AGATTAAAATGCCCA[C/T]ACAGTCAATGGGCAA | 23092 |
| rs385670 | snp | C/T | 0.453697 | 0.14494 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142905275 | AATAAAAGTGTGTGA[C/T]ATGAGAGTGCAAAAA | 23092 |
| rs388940 | snp | C/T | 0.302435 | 0.244439 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142796641 | TCAAGACGTCTGAAC[C/T]TTATCCTAAAAGGGC | 23092 |
| rs389003 | snp | A/C | 0.464416 | 0.128553 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809936 | GAAGCAATGATACTA[A/C]AACCTGCACCAGTCC | 23092 |
| rs389008 | snp | C/G | 0.487305 | 0.0786545 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889635 | CTCCCAATTTAAACT[C/G]TTATCTATTCCtttc | 23092 |
| rs392543 | snp | G/T | 0.40626 | 0.195148 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142810456 | AACAGACACAAAAAG[G/T]CATGTTCATTAAAAT | 23092 |
| rs392926 | snp | C/T | 0.476314 | 0.106217 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821743 | TACACAGAGTTGGCA[C/T]TGGAAATTGTCACCA | 23092 |
| rs394807 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142799385 | tcttgacaagcattt[G/T]tagaatggctactgt | 23092 |
| rs396482 | snp | C/T | 0.444533 | 0.157025 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142899966 | GATTTATCCTTCACT[C/T]ATAGTAAACAGAGCC | 23092 |
| rs398067 | snp | A/G | 0.320096 | 0.239972 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822852 | AGGCTAGAGGTTAGG[A/G]ATATAAAGGGAATAA | 23092 |
| rs398078 | snp | A/G | 0.417196 | 0.185864 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142817482 | CTGTCTTATGAACCC[A/G]GGACTGCAAGGCACC | 23092 |
| rs398398 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823165 | ATcctcagctccacc[C/T]tcagctccaccttca | 23092 |
| rs401531 | snp | A/C | 0.465473 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889263 | tttcatttttctcct[A/C]cagtgctcagaacgg | 23092 |
| rs402292 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787299 | AGTAGGTCAATAATT[A/T]ATATTTCAAGAAGGG | 23092 |
| rs405312 | snp | A/C | 0.420415 | 0.182917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921559 | CTATTCTGACTTTCA[A/C]CAATCTTCAGTTTTC | 23092 |
| rs405320 | snp | A/C | 0.420415 | 0.182917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921558 | TATTCTGACTTTCAC[A/C]AATCTTCAGTTTTCC | 23092 |
| rs405633 | snp | C/T | 0.376394 | 0.215696 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808274 | CTAAAATACAACATT[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs405668 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808237 | TTTTTTTTTTTTTTT[C/T]CCGAGACAATGTCTC | 23092 |
| rs407776 | snp | C/G | 0.496034 | 0.0443518 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142919161 | GCCCACCCTAATGAC[C/G]TCATTTTAACTTGAT | 23092 |
| rs409225 | snp | A/C | 0.224116 | 0.248656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142919162 | GGCCCACCCTAATGA[A/C]GTCATTTTAACTTGA | 23092 |
| rs409509 | snp | C/T | 0.485933 | 0.0826777 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909308 | AGGACCGAAGTGGAA[C/T]GCTTGTAGAGGACTA | 23092 |
| rs412738 | snp | C/T | 0.437683 | 0.165152 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886848 | TAAAAAGTCAGGGCA[C/T]CAAGACAGATTCTAA | 23092 |
| rs415235 | snp | A/G | 0.471768 | 0.115407 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906391 | cattttgcaaccatc[A/G]tagtaaagatcagct | 23092 |
| rs415786 | snp | A/T | 0.299158 | 0.245119 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804432 | ATTCAGTAAGTTTCC[A/T]TTCagtgagtgagcc | 23092 |
| rs417020 | snp | A/G | 0.471004 | 0.116864 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822752 | TCCAGATGAAGACCA[A/G]TAAGAAGCACACACA | 23092 |
| rs419418 | snp | A/G | 0.343701 | 0.231776 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142795799 | TGAGATTCTGGGGAT[A/G]AATTCAGCCCCTTTT | 23092 |
| rs421116 | snp | G/T | 0.300169 | 0.244914 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804629 | tggcacatgcctgta[G/T]tcccagctactcggg | 23092 |
| rs423856 | snp | C/T | 0.394538 | 0.203982 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804752 | gtaatcccagaactt[C/T]gggaagccaaggcag | 23092 |
| rs429459 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890153 | tatatatatatatat[A/T]ttttttttttttttt | 23092 |
| rs429465 | snp | C/T | 0.392696 | 0.205275 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804365 | CTTCCCAGAAGCATC[C/T]CTGGTTAGACCAAAA | 23092 |
| rs430109 | snp | C/T | 0.469445 | 0.119766 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888414 | AGTTCCCTCATAAAA[C/T]GTAATTCAAGAAAGT | 23092 |
| rs432699 | snp | C/T | 0.489796 | 0.070696 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142805392 | aatgtgggccaggcg[C/T]ggtgggtcacacctg | 23092 |
| rs433989 | snp | C/T | 0.127599 | 0.217986 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142804779 | TCAGCccgggcatgg[C/T]ggctcatgcctgtaa | 23092 |
| rs434456 | snp | A/G | 0.490343 | 0.0688145 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906186 | atgtggtgtcgacct[A/G]cccctcagtggtgat | 23092 |
| rs437716 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823304 | CTGATCATGTTACAG[A/G]AGCCATGCAGAAGCC | 23092 |
| rs439140 | snp | C/T | 0.455263 | 0.142713 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142797156 | TCTTAGAGGTATATC[C/T]GGGCTATTTAGTTCA | 23092 |
| rs439177 | snp | A/T | 0.271905 | 0.249038 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142798913 | GCATGGAGCCCCTTC[A/T]TCCACCAGGCCAAGC | 23092 |
| rs440447 | snp | A/G | 0.45235 | 0.146814 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142808503 | TGAGTGACACTAGCC[A/G]TATCTCACAGGTTGC | 23092 |
| rs447923 | snp | A/G | 0.425277 | 0.178263 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872692 | AAACACATGCCACAC[A/G]CAGTATCCATAAGAA | 23092 |
| rs448656 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142785443 | CAGAGGCCTAAAGGC[A/C]CCCTCGGCAGTGAGT | 23092 |
| rs452120 | snp | A/T | 0.382279 | 0.212137 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142809328 | CTCTCTTGGGGAACT[A/T]TTATTTACAGTAGAC | 23092 |
| rs452711 | snp | C/T | 0.455977 | 0.141681 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890944 | GATCCAGAAGGAAAT[C/T]CCTATAAGGAAAACA | 23092 |
| rs456583 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142906703 | CTTAGTGTATTCTTA[A/C]AGACTGGGGAAAAAA | 23092 |
| rs458834 | snp | A/G | 0.325327 | 0.238382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848332 | CCCCGGGGAGTGATG[A/G]CCACCCAGTCCTGTA | 23092 |
| rs462586 | snp | G/T | 0.325091 | 0.238456 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142845674 | TGCTTTAGCTGATTT[G/T]AGTACTGAGAAGCTG | 23092 |
| rs463717 | snp | A/C | 0.432063 | 0.171327 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871325 | CACTCCCTGATCCTC[A/C]TGGCAGCTGCCCTTG | 23092 |
| rs586084 | snp | C/G | 0.461813 | 0.132798 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142890268 | TTTAACTTCAACATA[C/G]AGTAAGAAATACTTT | 23092 |
| rs690069 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887738 | acctcTTTAGTGTTA[G/T]ATGTTTATACAGTTT | 23092 |
| rs690070 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142887735 | tcTTTAGTGTTATAT[G/T]TTTATACAGTTTAAT | 23092 |
| rs690611 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878785 | cgtttgaggtgcatt[G/T]gagtgccagtaggtt | 23092 |
| rs696521 | snp | C/T | 0.497695 | 0.0338674 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966242 | GATACCTGAGAGCTG[C/T]CTGTGTAGGTGTGCA | 23092 |
| rs698287 | snp | C/T | 0.499673 | 0.0127754 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925866 | AAGATCTAGAATTTA[C/T]TCATTCATAAGACTA | 23092 |
| rs698288 | snp | A/G | 0.498059 | 0.0310896 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965889 | TATTTACACTGGATG[A/G]CTTTCAAAAACTCCC | 23092 |
| rs707177 | snp | C/T | 0.422473 | 0.180978 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872327 | TGGTGGGGGGGTGTA[C/T]TGTGGCTGCACAGAT | 23092 |
| rs712157 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142893866 | gacacacaaatagcc[A/C]aagggtatattaaaa | 23092 |
| rs712158 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895787 | cagttgcccaggctg[A/G]tctcaaactcttggt | 23092 |
| rs712159 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895796 | tatgttgcccagttg[A/C]ccaggctgatctcaa | 23092 |
| rs712161 | snp | G/T | 0.496279 | 0.0429702 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912163 | ATAGCACTAGTTTAT[G/T]GCCCAGAAACACAGA | 23092 |
| rs712164 | snp | A/G | 0.436692 | 0.166271 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918426 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 23092 |
| rs712165 | snp | A/G | 0.436834 | 0.166111 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918600 | ATTAGAGGAGATGTG[A/G]CCTCTGAAATCATGT | 23092 |
| rs712166 | snp | C/T | 0.420415 | 0.182917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142918788 | CTAACTTTAGCTTTT[C/T]GATGTTAGGAACAAT | 23092 |
| rs712167 | snp | C/G | 0.441295 | 0.160954 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926109 | ACCAACTCATAGCCT[C/G]CTCACCAGCCAAGAG | 23092 |
| rs712168 | snp | A/G | 0.499642 | 0.0133738 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928371 | GCTACTCTAGGCAAC[A/G]AGCTAATCCAAAACA | 23092 |
| rs712169 | snp | A/G | 0.430136 | 0.173352 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929581 | GTCTTGTTCCCTTTT[A/G]CAGGGGAAGTGGGGT | 23092 |
| rs712170 | snp | G/T | 0.465578 | 0.126594 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930592 | GAAAGGGGAGTGGGG[G/T]TGTATGTGGGTGGGA | 23092 |
| rs712172 | snp | C/T | 0.45866 | 0.137698 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930784 | TCATTAACCATTCCT[C/T]GACATCCCCTTAAAA | 23092 |
| rs712175 | snp | A/G | 0.458545 | 0.137872 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930932 | AGCAGCACAAGCCTG[A/G]GCCCCATATGCACCC | 23092 |
| rs712176 | snp | C/T | 0.441432 | 0.160792 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931877 | TACTCTCAGAAAGGA[C/T]GGCCCAAATTCCTCT | 23092 |
| rs712177 | snp | A/G | 0.449218 | 0.151037 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142931944 | AGTCAGTGGCTGCTA[A/G]GGTTAACAACACAAA | 23092 |
| rs712178 | snp | A/G | 0.499958 | 0.00459246 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142939736 | GACTGTCATTTTCCA[A/G]TTTGAGACTGCCAAT | 23092 |
| rs712180 | snp | C/T | 0.437683 | 0.165152 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950342 | CTTCATTTTGATTAG[C/T]GTATATACTTTCCTT | 23092 |
| rs712181 | snp | A/G | 0.450859 | 0.148847 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955770 | TAACATCTGGAACCG[A/G]TCATTTGTCTATTTC | 23092 |
| rs712182 | snp | A/G | 0.419776 | 0.18351 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956029 | CTTTGAATATTCTCA[A/G]ATAATTCCCTGTTGT | 23092 |
| rs712183 | snp | C/T | 0.438806 | 0.163867 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956387 | gttcttgctgtgttg[C/T]ccagtctggtcttga | 23092 |
| rs712184 | snp | C/T | 0.434831 | 0.168337 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142956909 | ccggtatttcccatc[C/T]tattcttatgatagt | 23092 |
| rs712185 | snp | C/T | 0.43598 | 0.167067 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958606 | GATCACAGTTCACTG[C/T]AGCCTCAACCTCCTG | 23092 |
| rs712186 | snp | C/T | 0.444931 | 0.15653 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142960105 | GTCCTAGCTGTCTTA[C/T]TTGGATGAGACAGCT | 23092 |
| rs712187 | snp | A/G | 0.498109 | 0.0306926 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965962 | GGCTTATTTAGAACC[A/G]GCTATTAAAGATTAA | 23092 |
| rs712188 | snp | A/C | 0.34526 | 0.23114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156852 | GATGGAAAGTGCAGC[A/C]CTGGTGAGCTAATAG | 23092 |
| rs713141 | snp | G/T | 0.084364 | 0.187256 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142821922 | TTTTTGTCCTACATA[G/T]ATTAATTGACATGAG | 23092 |
| rs715366 | snp | A/C | 0.245631 | 0.249962 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102394 | CTGCATGTTTGGGGC[A/C]GACACTGAGGTCTTT | 23092 |
| rs717407 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954653 | TGCTACTGTGTGCCA[G/T]ATAATATGCCACCTG | 23092 |
| rs717408 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954531 | ACAAGGAACCTGAGT[A/G]TTCTTAAGAGACACA | 23092 |
| rs721473 | snp | A/G | 0.031825 | 0.122064 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059204 | AGCATCCCCACACAT[A/G]CTAGGCTGGAGGGTG | 23092 |
| rs724301 | snp | C/T | 0.369958 | 0.21934 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786276 | tgtaagccatggtgt[C/T]tggccCTAATACATT | 23092 |
| rs728463 | snp | A/C | 0.476574 | 0.105661 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004805 | TGGTTCTTGTTGGCT[A/C]CACCCTCTGGCTCTG | 23092 |
| rs728464 | snp | C/T | 0.472147 | 0.114677 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004606 | AAGGCAGATTTCAGC[C/T]GAACATAAATGACTG | 23092 |
| rs728465 | snp | A/G | 0.4711 | 0.116682 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143004595 | CAGCCGAACATAAAT[A/G]ACTGACAGGAGCTCT | 23092 |
| rs740010 | snp | G/T | 0.0799831 | 0.183287 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135316 | TGAGGATTAAGGCCC[G/T]TCAAATGTTGCCAGG | 23092 |
| rs740572 | snp | G/T | 0.341235 | 0.232758 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107171 | AAACACACCAAGTAT[G/T]CTCACACCCAATACC | 23092 |
| rs740573 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115754 | aaatgggagcaataa[C/T]atgtagcttgtagct | 23092 |
| rs740574 | snp | C/T | 0.421051 | 0.182323 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114803 | TCCCATGGGATTGAC[C/T]GTGACGTATCTCTTA | 23092 |
| rs829543 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813208 | cacgcctgtaatccc[A/C]gcactttgggaggcc | 23092 |
| rs829544 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813202 | tgtaatccccgcact[C/T]tgggaggccaaggcg | 23092 |
| rs829553 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833267 | tatgttgcccagttg[A/C]ccaggctggtctcaa | 23092 |
| rs829554 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833276 | cagttgaccaggctg[A/G]tctcaaactcctggc | 23092 |
| rs829555 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833304 | ggcctcaggtgatct[G/T]cctgcctcagcctcc | 23092 |
| rs829556 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142833319 | gcctgcctcagcctc[C/T]caaagtgctaggatt | 23092 |
| rs829754 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895759 | ggtctcaagtgatct[G/T]cctgcctcagcctct | 23092 |
| rs829755 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895744 | tcctgcctcagcctc[C/T]caaagtgctaggatt | 23092 |
| rs830286 | snp | C/T | 0.497641 | 0.0342639 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967329 | TAAACTGATGCCACA[C/T]ACACCTTCTAACCGC | 23092 |
| rs830287 | snp | A/C | 0.495868 | 0.0452663 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142967146 | CATTACAGCACTAAA[A/C]GAACATTAAGAATAA | 23092 |
| rs830288 | snp | A/C | 0.498206 | 0.0298983 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966732 | TAAAGTAAAATAAAA[A/C]ATTTGAAAAAAGATA | 23092 |
| rs830289 | snp | C/T | 0.498084 | 0.0308911 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965578 | ctctataatcataac[C/T]taggaaaaaccaggc | 23092 |
| rs830290 | snp | A/G | 0.498158 | 0.0302955 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142965442 | agcggtgatgccagc[A/G]tctgggaagacgccc | 23092 |
| rs830297 | snp | A/G | 0.434976 | 0.168179 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142955266 | TCGCCCAGTCTGGAG[A/G]GCAGTGGTAATGATC | 23092 |
| rs830301 | snp | A/G | 0.491525 | 0.0645418 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935958 | agtaagagtggtgac[A/G]gcaaacaccctcaac | 23092 |
| rs830302 | snp | A/G | 0.154238 | 0.230932 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142935926 | tgttcctagtcttag[A/G]gggaaagcattcagt | 23092 |
| rs830532 | snp | A/G | 0.443195 | 0.158668 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142909976 | TTCTAGTAACTCTCT[A/G]AAGTCTCTGGAGAAC | 23092 |
| rs853158 | snp | A/G | 0.45574 | 0.142025 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143225607 | TGAAGCTGGGGCCAA[A/G]TGTCTACAGGGATGC | 23092 |
| rs853159 | snp | C/T | 0.32768 | 0.237625 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186778 | ACAGCCCTGTCACTG[C/T]GTCTGCACAGCAAAG | 23092 |
| rs853160 | snp | A/C | 0.350764 | 0.228794 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179527 | CAGGGCCAAAAGCCT[A/C]CAGGCATAGCTCACA | 23092 |
| rs853161 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143178889 | gagtgagactccttg[A/G]aaaaaaaaaaaaaTC | 23092 |
| rs853162 | snp | C/T | 0.318174 | 0.240525 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174218 | AACAACATACCCAAC[C/T]GGATCCTTAACACTG | 23092 |
| rs853163 | snp | C/T | 0.440057 | 0.162414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143173517 | AAATGTTGACTCTTA[C/T]TAATAAAACAATGCA | 23092 |
| rs853164 | snp | C/T | 0.406814 | 0.194704 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172163 | CAGAATTTGTCAGCA[C/T]ACAAAGACTTGAAAT | 23092 |
| rs853165 | snp | C/T | 0.49121 | 0.0657086 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170686 | TCTATGCCTCATGTG[C/T]AAAATGTGGAGTACA | 23092 |
| rs853166 | snp | A/G | 0.404559 | 0.196498 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170524 | TTTCAACCTTTGAGA[A/G]CAAAATTTGTTCTCA | 23092 |
| rs853167 | snp | G/T | 0.499946 | 0.00519141 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169255 | ACCAAGAACACTGAT[G/T]GGTAAATCTGCTCAA | 23092 |
| rs853168 | snp | C/G | 0.390838 | 0.206555 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159199 | GCAGGGGGAAGGAGA[C/G]GGCCAAGGCATTTAT | 23092 |
| rs853169 | snp | C/T | 0.340108 | 0.233197 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158852 | AACATCTTGGTTTTC[C/T]CTGAAGACAAGGCTT | 23092 |
| rs853170 | snp | A/G | 0.441432 | 0.160792 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157909 | TTCCCAAGTTTACAC[A/G]GTTAGGAAATGGCAG | 23092 |
| rs853171 | snp | A/G | 0.436123 | 0.166908 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157423 | TGGGAGGCTGAGGCA[A/G]GTGGATCACTTGAGG | 23092 |
| rs853172 | snp | A/C | 0.497722 | 0.0336691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157169 | AAAAAAAAAAAAGAA[A/C]GAATGTGTTGAACTT | 23092 |
| rs853173 | snp | C/T | 0.438526 | 0.164189 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156992 | CTTGATCTTTTCATG[C/T]TACACACACAATAGA | 23092 |
| rs863805 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813155 | aggagatcaagacca[G/T]cctggttaacacggt | 23092 |
| rs864364 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142813165 | tcacgaggtcaggag[A/T]tcaagaccagcctgg | 23092 |
| rs865481 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203664 | ggcatttgggttggt[A/T]ccaagtctttgctat | 23092 |
| rs865526 | snp | A/T | 0 | 0 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142969121 | agcccccttctctat[A/T]aataataataataat | 23092 |
| rs865527 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142941129 | acctagcaatcccat[G/T]gggtatatacccaat | 23092 |
| rs963104 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143188535 | TGGTACTCTACTATA[C/T]ATACTCAAATTTTCT | 23092 |
| rs975981 | snp | C/T | 0.16028 | 0.233346 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098335 | TAAAAAAATCACCTA[C/T]GTTATTGTTAAAATG | 23092 |
| rs975982 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098229 | TATTAAAGAAGAATA[C/T]ATGGTCTGAACCCTA | 23092 |
| rs984552 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142811342 | ATGTGGACAGCTTGG[G/T]TGACCACAGCACATT | 23092 |
| rs986563 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167540 | CGTTGTTTGTAATAA[A/G]AATAGGGGCGCTCAA | 23092 |
| rs986564 | snp | A/T | 0.132066 | 0.220435 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167596 | AGTTGTTCATCAATG[A/T]TGTAGATTGTGTATC | 23092 |
| rs1003926 | snp | A/C | 0.191461 | 0.24305 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218079 | taaagctttatttac[A/C]aaaacaggtggcggg | 23092 |
| rs1003927 | snp | C/T | 0.458315 | 0.13822 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218049 | gttggatttgactgg[C/T]aggtcatagtttgct | 23092 |
| rs1009467 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172532 | TCAAAATCATTAATA[C/T]AGAGATTCACATGAC | 23092 |
| rs1010109 | snp | C/T | 0.228842 | 0.249103 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174597 | TTTTACATTAATCTA[C/T]TGCTTGGAATGGCTA | 23092 |
| rs1036596 | snp | A/G | 0.451732 | 0.147663 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034983 | CCTTAAAATGGTAAG[A/G]AGCCTATTAACCCAA | 23092 |
| rs1054034 | snp | C/G | 0.446488 | 0.154572 | intron-variant, nc-transcript-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142860089 | ggatgtcatgcgggc[C/G]cactggggctccttg | 23092 |
| rs1096247 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963172 | gtatatatatatata[C/T]atatataccatggaa | 23092 |
| rs1096248 | snp | C/T | 0.444267 | 0.157354 | intron-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142963164 | atatatatatatata[C/T]catggaatactacac | 23092 |
| rs1155226 | snp | A/G | 0.39121 | 0.2063 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142790609 | gacgcctgatcatac[A/G]aggccgcatgaacca | 23092 |
| rs1155433 | snp | A/G | 0.468949 | 0.12067 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008334 | TGTCTGTCAGTGGCG[A/G]CAGATTTGTAGTAAT | 23092 |
| rs1160959 | in-del | -/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896008 | TAACTTCCAGCAGTG[-/T]GGTTTCAGTCAAGGT | 23092 |
| rs1347813 | snp | A/G | 0.473266 | 0.112482 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019729 | TTTGTTATTTAAAAC[A/G]TCAAACTTGGAAAAG | 23092 |
| rs1370982 | snp | C/T | 0.431325 | 0.172108 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143001519 | AAACATGCATATACC[C/T]ATCACCTCCATTCTA | 23092 |
| rs1370985 | snp | A/G | 0.0236373 | 0.106113 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221450 | AAAAAAAAAACCCCA[A/G]AAAATTTGCAAGGAA | 23092 |
| rs1438724 | snp | A/C | 0.474634 | 0.109726 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005576 | GTTCAACATCCATGC[A/C]CCTCTTTTTCCAGGG | 23092 |
| rs1438725 | snp | G/T | 0.0573587 | 0.15934 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005447 | ATGTGATCCAGACTA[G/T]GCATCCTACTGCACA | 23092 |
| rs1438733 | snp | A/T | 0.463881 | 0.12944 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149816 | TAACTTGACTATTAA[A/T]TATGCATGAGGTAGG | 23092 |
| rs1438734 | snp | A/G | 0.476314 | 0.106217 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143217059 | TATGAGGTAAAGGCT[A/G]TTTAATTTGTATGCT | 23092 |
| rs1541448 | snp | A/G | 0.45889 | 0.13735 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143028259 | ACAGCAATGATAACC[A/G]TGGCTAACACTTACT | 23092 |
| rs1612480 | snp | C/T | 0.475437 | 0.108066 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775816 | taggatttcatttct[C/T]ttcatggctaaatat | 23092 |
| rs1613212 | snp | A/G | 0.476833 | 0.105105 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775869 | CAACAGCTGTCATTA[A/G]GAAAGACTATTCTTT | 23092 |
| rs1613324 | snp | C/T | 0.489837 | 0.0705577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775905 | TTAAAGTCATAAAAA[C/T]GTATTTTTTTCTTTC | 23092 |
| rs1635443 | snp | A/G | 0.436408 | 0.16659 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157840 | CACAGGCTTTGCCCT[A/G]CCCCAGATTCTAAAG | 23092 |
| rs1635456 | snp | C/T | 0.475965 | 0.106957 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154061 | GTTGACCAACTAAAG[C/T]GGAAGATTAGTAAAA | 23092 |
| rs1644057 | snp | C/T | 0.174288 | 0.23826 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786045 | AGTCTGAGGGTACAG[C/T]GAGCTATGACTGTAC | 23092 |
| rs1644058 | snp | A/G | 0.174932 | 0.238463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784995 | agcttgcagtgagcc[A/G]agatcgcgccactgc | 23092 |
| rs1644059 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784072 | AGGCCGGCAGATTGT[G/T]GCAAGTCCTGGCCAG | 23092 |
| rs1644060 | snp | A/G | 0.440195 | 0.162252 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776877 | tcatacattgttggt[A/G]ggaatgtgaaacggt | 23092 |
| rs1659182 | snp | A/G | 0.499918 | 0.00638925 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157367 | TGTTTTGGCAGAGAC[A/G]GCGTTTCACCATGTT | 23092 |
| rs1659183 | snp | C/G | 0.43655 | 0.16643 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157369 | TTTTGGCAGAGACAG[C/G]GTTTCACCATGTTGG | 23092 |
| rs1659186 | snp | C/T | 0.342582 | 0.232225 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157845 | GAATCTGGGGCAGGG[C/T]AAAGCCTGTGTGGCC | 23092 |
| rs1659194 | snp | A/C | 0.475877 | 0.107142 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154060 | ATTTTACTAATCTTC[A/C]ACTTTAGTTGGTCAA | 23092 |
| rs1799290 | snp | A/G | 0.476746 | 0.10529 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775711 | ctgtgtacttcttat[A/G]agtggaattatacaa | 23092 |
| rs1799291 | snp | A/G | 0.176219 | 0.238865 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791532 | TCTTCTAGGTGTGAA[A/G]ATTAGGAAACACATC | 23092 |
| rs1799293 | snp | C/G | 0.490782 | 0.0672626 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783580 | GAGGAGAGAGACTGG[C/G]TGATGGCTCTGGAGC | 23092 |
| rs1799294 | snp | C/G | 0.175254 | 0.238565 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142784511 | TCTAATCCTTACTGC[C/G]CCTAAACTGAGTCTC | 23092 |
| rs1813186 | snp | G/T | 0.233527 | 0.249457 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016553 | ACCATGCCTGGCTAA[G/T]TTTTGTATTTTTAGC | 23092 |
| rs1821253 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787246 | GTCTCATTTTTATCA[C/T]TGGGGTGGGAGAGTG | 23092 |
| rs1837261 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142972500 | ATACAATACAAAGGT[C/T]TGGGATTAATTTAAG | 23092 |
| rs1946836 | snp | A/G | 0.222928 | 0.24853 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208266 | GTGGAGCTCCTAAAC[A/G]TGCTTCTCTCTCAAG | 23092 |
| rs1972625 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942901 | accagctactcagga[A/G]gctgaggcaggaaaa | 23092 |
| rs1972626 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142942858 | GGGAGGCAGAGGTTG[C/T]AGTGAGCTGAGATCC | 23092 |
| rs2005205 | snp | G/T | 0.408871 | 0.193029 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106620 | TGGGACTACAGGCAC[G/T]TGGCACCACGCCCAG | 23092 |
| rs2005795 | snp | A/G | 0.448323 | 0.15221 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106790 | TGCCTGCCTGAGACC[A/G]CTTTAAAATGAAGCC | 23092 |
| rs2005796 | snp | C/G | 0.316243 | 0.241064 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143106623 | TAGCTGGGCGTGGTG[C/G]CACGTGCCTGTAGTC | 23092 |
| rs2028267 | snp | C/G | 0.353371 | 0.227628 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195006 | TGAACAGATTAAAAT[C/G]AGATCAGAGACAATT | 23092 |
| rs2028268 | snp | A/G | 0.359152 | 0.224913 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195222 | TTAATCATCCTGGAC[A/G]TTGTCCTTGCAGAAG | 23092 |
| rs2067142 | in-del | -/TCCTCTC | 0.497749 | 0.0334707 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142949328 | AAGTGATGAATATGT[-/TCCTCTC]TCCTCTCTATGAACA | 23092 |
| rs2074635 | snp | A/G | 0.450859 | 0.148847 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207966 | AACGAGGCATAAGCC[A/G]TGAGCAATTTAAGAG | 23092 |
| rs2074636 | snp | C/T | 0.466515 | 0.124985 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143207129 | GAGCACAGGAGGTCA[C/T]GGGAGGCCAGATGAC | 23092 |
| rs2074637 | snp | C/T | 0.378765 | 0.214288 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206817 | CTTCAGCTTCCACTC[C/T]TGTGGGAGTGTTTTT | 23092 |
| rs2098050 | snp | G/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115350 | TTCTTTCGttttttg[G/T]tgttgttgttgtttt | 23092 |
| rs2107622 | snp | C/T | 0.36315 | 0.222928 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143171832 | CTGGGATTGTGCCTA[C/T]GCCAGAGATAAATAC | 23092 |
| rs2107626 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223065 | TGTTCCCGTGCATGA[A/G]AAGACTGGATTGTAT | 23092 |
| rs2108645 | snp | A/G | 0.215446 | 0.2476 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079942 | CTCTGGAGCTATGTG[A/G]CAGCTGGCTTGGTCT | 23092 |
| rs2108843 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093610 | aggaggagacaaaga[C/T]ggagtcaaagacaga | 23092 |
| rs2108844 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116555 | ATCACATCTGTTTTC[C/T]TAGAGTTTAAATGAG | 23092 |
| rs2108845 | snp | A/T | 0.0715223 | 0.175059 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112645 | AGTTGAAAAGTAGAA[A/T]GATGGTTGCCAGGGG | 23092 |
| rs2190778 | snp | A/T | 0.123105 | 0.215401 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058569 | AACTGTTATGCTCTC[A/T]TTCTTTTCTTGTGCT | 23092 |
| rs2190779 | snp | C/G | 0.442655 | 0.159323 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058365 | TTTGATTATCTCAGA[C/G]GACAAGTGAGTATTT | 23092 |
| rs2270067 | snp | C/T | 0.123798 | 0.215808 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143057506 | CAATCCTGTCTTGTG[C/T]GCATACTGCGTGGCC | 23092 |
| rs2270068 | snp | A/C | 0.0732493 | 0.176803 | synonymous-codon, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143041850 | CACTCTGGAGTTGAC[A/C]CCCACAATTCGATAC | 23092 |
| rs2276991 | snp | C/G | 0.000831601 | 0.0203742 | intron-variant, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770967 | GGCTAAGCGCCACCT[C/G]CCAGTTCCTCCCGCC | 23092 |
| rs2276992 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770705 | gcccgggccgcccgc[A/C]gcccAGAGCACTCAC | 23092 |
| rs2276993 | snp | C/T | 0.338523 | 0.233803 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:142770637 | GCTCCACAGGTGTGG[C/T]GCTGGCTCACTCCGC | 23092 |
| rs2278380 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142932524 | AACAACTACAAGATT[A/G]CATCACCCAGCTGAG | 23092 |
| rs2286013 | snp | A/G | 0.0401234 | 0.135837 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133958 | TAAATATCTGCAAAC[A/G]AAGTTTCACAACAAG | 23092 |
| rs2302100 | snp | C/T | 0.432357 | 0.171014 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143055823 | TCTTAAATGAATAGA[C/T]ACAACTATGTTTCAT | 23092 |
| rs2304040 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142903818 | AGATTCTGTGGACAT[A/C]ATCTTTCTCTTTGGA | 23092 |
| rs2304041 | snp | C/T | 0.232943 | 0.249417 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142894592 | TCATATGGCACATCA[C/T]TGGGTAGCCAGAGGA | 23092 |
| rs2398565 | snp | A/G | 0.121022 | 0.21416 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143053846 | TAGAAAAAGTTTCTC[A/G]TAGACATATCTTGTT | 23092 |
| rs2398609 | snp | C/T | 0.095934 | 0.196885 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101051 | TGAACAAACATTGTG[C/T]CACTACACTCCAGCC | 23092 |
| rs2398610 | snp | A/G | 0.341235 | 0.232758 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104817 | aactaggtgtctgca[A/G]tatgattccaacttg | 23092 |
| rs2398611 | snp | C/T | 0.450021 | 0.149972 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104851 | tgaaatatgagtgtg[C/T]gtgtgtctgaaaaaa | 23092 |
| rs2398612 | snp | C/T | 0.354881 | 0.226936 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143104882 | acatggaatgtgaca[C/T]gtataccttaaaaca | 23092 |
| rs2398613 | snp | C/T | 0.409212 | 0.192748 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105040 | TTTTTTTCCCCCTAA[C/T]GATAGCACTGAAAGA | 23092 |
| rs2398614 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114140 | CAATTAATTATTTCA[A/G]GCTTCCTGTCTGGCT | 23092 |
| rs2398615 | snp | A/G | 0.137527 | 0.223271 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115312 | CACTCCAGCCTGCAC[A/G]ACAAGAGTGAAACTT | 23092 |
| rs2398616 | snp | A/G | 0.44546 | 0.155869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116002 | GATAAAAATAGAATC[A/G]ACAGGATAAGATGGG | 23092 |
| rs2398617 | snp | G/T | 0.451379 | 0.148143 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208247 | CCTGCAGAATTCCTA[G/T]GCTGTGGAGCTCCTA | 23092 |
| rs2436373 | snp | C/T | 0.206336 | 0.246157 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880410 | TAGTTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 23092 |
| rs2436374 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880429 | aggctgaggcaggag[A/G]attgcttgagccccg | 23092 |
| rs2436375 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880432 | ctgaggcaggaggat[C/T]gcttgagccccggag | 23092 |
| rs2436376 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880439 | aggaggattgcttga[A/G]ccccggaggtcaagg | 23092 |
| rs2436377 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880443 | ggattgcttgagccc[A/C]ggaggtcaaggctgc | 23092 |
| rs2436378 | snp | A/G | 0.455977 | 0.141681 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142816091 | gcacagaggggctgg[A/G]caccatggttcacac | 23092 |
| rs2436379 | snp | C/T | 0.4231 | 0.180378 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142814886 | GCAGAGGCTAATAAC[C/T]GGCTAATAACTATTG | 23092 |
| rs2436380 | snp | A/C | 0.324145 | 0.238752 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142851384 | TCCGGCTGGGCGCAG[A/C]GGCTCACGCCTGTAA | 23092 |
| rs2438602 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900611 | TCATCCCGCCCCCCC[C/T]CCCCTACTCTCCCAC | 23092 |
| rs2545746 | snp | G/T | 0.498459 | 0.0277128 | | | GRCh38.p7 | 5:142964545 | tgtgtgtgtgtgtgt[G/T]ttttaaacagagaaa | 23092 |
| rs2545747 | snp | A/G | 0.5 | 0 | | | GRCh38.p7 | 5:142963223 | ggtacacacacacac[A/G]cgcacacacacacac | 23092 |
| rs2545748 | snp | A/G | 0.473543 | 0.111932 | | | GRCh38.p7 | 5:142963221 | tacacacacacacgc[A/G]cacacacacacacac | 23092 |
| rs2569057 | snp | G/T | 0.498034 | 0.0312882 | | | GRCh38.p7 | 5:142955126 | TGTGCAGAGATGGGG[G/T]GTGTGTGTGTGTGTG | 23092 |
| rs2578588 | snp | C/T | 0.5 | 0 | | | GRCh38.p7 | 5:142941101 | AATGGAATATAGATT[C/T]TTTTTTTTTTTTTTT | 23092 |
| rs2578589 | snp | C/T | 0.439224 | 0.163383 | | | GRCh38.p7 | 5:142940839 | tctgcccacctcggc[C/T]tcccaaagtgctggg | 23092 |
| rs2578593 | snp | A/T | 0.492484 | 0.0608394 | | | GRCh38.p7 | 5:143044756 | AAATTGGAGCCAACA[A/T]TATGCTCCTAATGCT | 23092 |
| rs2578596 | snp | A/G | 0.48378 | 0.0885831 | | | GRCh38.p7 | 5:143045810 | GGGTTTCACCATGTT[A/G]GCCTGGCTGCTCTCG | 23092 |
| rs2578598 | snp | A/G | 0.483418 | 0.0895317 | | | GRCh38.p7 | 5:143045723 | GGCATGAGCCACCGC[A/G]CCTGACCAGCCATAT | 23092 |
| rs2578602 | snp | C/T | 0.339882 | 0.233284 | | | GRCh38.p7 | 5:143158902 | ACCTTGAATGAACAC[C/T]TTTGCCTTTGTTTGT | 23092 |
| rs3059587 | in-del | -/TTT | 0.5 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142791097 | ttttttttttttttt[-/TTT]gagacagagtctcgc | 23092 |
| rs3059615 | in-del | -/GT/TG | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142878545 | catgtgtgtgtgtgt[-/GT/TG]ATAAATGTGTAGTGT | 23092 |
| rs3059616 | in-del | -/TC | 0.203267 | 0.245593 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142880908 | CTGTGGCAAAGACTT[-/TC]TCCCAGTTTTAGAGT | 23092 |
| rs3073231 | in-del | -/A/AT/ATAT/ATATATATATAT/ATATATATATATAT/ATATATATATATATATATATATATATA | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012576 | TATATATATATATAT[lengthTooLong]TATGATCAGGTTCAC | 23092 |
| rs3074353 | in-del | -/AA/AAAAA/AAAAAA/AAAAAAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143154173 | TTAAAAAAAAAAAAA[-/AA/AAAAA/AAAAAA/AAAAAAA]GAGTTTCTGCTTTCA | 23092 |
| rs3216968 | in-del | -/A | 0.0228947 | 0.104514 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143147104 | AGGGAAGCTTAAGAA[-/A]CAACATAGAAAAGGT | 23092 |
| rs3217375 | in-del | -/CTACC | 0.375 | 0.216506 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907602 | ATTCATAATGCTCAT[-/CTACC]CTACCCTTAAACTAT | 23092 |
| rs3733729 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143221293 | ATTCTTCTCTTCCTC[C/T]CTCTATTGCCCTTTG | 23092 |
| rs3733731 | snp | C/T | 0.499354 | 0.0179596 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143216850 | TTGAGCTAACCCAAT[C/T]GAGAAAGTGTACTAA | 23092 |
| rs3733732 | snp | C/G | 0.303438 | 0.244222 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867168 | GAACACCTTGACCAA[C/G]CAGCTAATTTAAACA | 23092 |
| rs3733733 | snp | G/T | 0.305436 | 0.243776 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142867009 | CCCTGGCTTCCACAT[G/T]GGAAGAAGTGCTCTA | 23092 |
| rs3733734 | snp | A/G | 0.204189 | 0.245767 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819602 | TGTTCAGGTAACATC[A/G]GTTTGTGTAATCCAG | 23092 |
| rs3733735 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142819306 | ACTCCCCACTGCAAG[A/G]ACCATGGTTGACCTC | 23092 |
| rs3756368 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186619 | CAATCCTGAGCTCTG[G/T]CTCATTTATGAAACT | 23092 |
| rs3756371 | snp | C/T | 0.104149 | 0.203046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149910 | TCTCTCTGGTCATAA[C/T]GATATCCCAGTCATT | 23092 |
| rs3756373 | snp | A/T | 0.104504 | 0.2033 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138055 | GGTCTACTCACACTG[A/T]AGGAAAAACCCCTTC | 23092 |
| rs3756374 | snp | A/C | 0.406814 | 0.194704 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138036 | AAAAACCCCTTCTGG[A/C]AAATAAGACACACAT | 23092 |
| rs3756375 | snp | A/G | 0.264632 | 0.249571 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131693 | CTTACAATGCCACAC[A/G]GCTAAGCAGGAGAGT | 23092 |
| rs3756376 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085817 | TCAGGACATTCTTTC[A/G]GTTAAGGAGGTTTGT | 23092 |
| rs3756377 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085792 | GTTTGTTTCCTTCCT[C/T]GTACCCACAGCCACT | 23092 |
| rs3756378 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079553 | ACCAGGCTGGTTGTC[C/T]CGTGTCTGGCACACC | 23092 |
| rs3756379 | snp | C/T | 0.175576 | 0.238665 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079489 | ATCAGCTGCACAGCA[C/T]CGTTAACTCTGAAAA | 23092 |
| rs3756380 | snp | C/T | 0.240765 | 0.249829 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062895 | TTGGACTAGTCTTGA[C/T]GGCAAATGAATAACT | 23092 |
| rs3756381 | snp | A/C | 0.215144 | 0.247558 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062862 | CACTTCTCATGTTTA[A/C]CAGCTCATTGGTAAG | 23092 |
| rs3756387 | snp | C/T | 0.443732 | 0.158012 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023471 | GTGGATTTTTGGTAA[C/T]GGCTGAAGGCTTTAG | 23092 |
| rs3756388 | snp | C/G | 0.0799831 | 0.183287 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015146 | TTTTTTGGAGGTGGA[C/G]GGGAACATTTTTTTT | 23092 |
| rs3756393 | snp | A/C | 0.0267878 | 0.112589 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142971097 | CATCTCTGAAAAAAA[A/C]TTATTTTCAAATTTG | 23092 |
| rs3756395 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953874 | GGTTCTGTGGGAAGT[C/T]CTCTTTAGTGCCAAA | 23092 |
| rs3756396 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142953857 | TCTTTAGTGCCAAAC[A/T]GAGACAGCTCTGTGC | 23092 |
| rs3756397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930539 | GGCGTGTTGATGATG[A/G]TGGAACACTGATCCC | 23092 |
| rs3756398 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142913677 | TACTAACTTTTTCAG[A/T]TAAAAAAAATTCAAA | 23092 |
| rs3776217 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143215269 | ATTGGGACTTAGAGG[A/G]CAGACCTTTAAGCCC | 23092 |
| rs3776221 | snp | C/T | 0.445987 | 0.155207 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210668 | GTGGAAAGGGGTTGA[C/T]CATTTAGGCATAATT | 23092 |
| rs3776224 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206592 | TTACCAGCAGAATGC[A/G]GTTCCTCTGAGGTTT | 23092 |
| rs3776225 | snp | A/G | 0.38555 | 0.210062 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143206255 | CAGTTCAGCCACACC[A/G]CCACTTGCCACTCCT | 23092 |
| rs3776226 | snp | A/G | 0.183886 | 0.241099 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205383 | TTCATATAGCAGATG[A/G]CATTCATATAAGAGA | 23092 |
| rs3776227 | snp | A/C | 0.176861 | 0.239062 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143201610 | GTAGAATCTTAAATT[A/C]TCCTTTCACTACAGA | 23092 |
| rs3776230 | snp | A/G | 0.349452 | 0.229367 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187982 | AAAGTGTCCTGTGAG[A/G]TGGAATGCTCTCATT | 23092 |
| rs3776231 | snp | C/T | 0.148326 | 0.228391 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186397 | AGTCCCTAGGCACTG[C/T]TGTGGATGGCTTCTT | 23092 |
| rs3776232 | snp | C/G | 0.308661 | 0.24302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186261 | TCTTAAAAGCAGCAT[C/G]ACATAACGTTTCATA | 23092 |
| rs3776233 | snp | C/T | 0.212232 | 0.247131 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186178 | TGATATTATAATATT[C/T]CACAAGGTGAGTGAC | 23092 |
| rs3776234 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184347 | TATACATGTTTTTAC[A/G]GGAGAGACAAAAGGA | 23092 |
| rs3776235 | snp | C/T | 0.175897 | 0.238765 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183933 | GCAGGAGCATCAATC[C/T]TTAAAAACTACAGGT | 23092 |
| rs3776236 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143179592 | GGCTTGCAGCTAAGA[A/T]CTCTCCTTCTCTCCC | 23092 |
| rs3776238 | snp | C/T | 0.365853 | 0.221536 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143175367 | CACATTTTCCTTCAC[C/T]GTCACCACAGAGTGC | 23092 |
| rs3776240 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143174875 | GACAGGTATGAGGCT[C/T]AGAAGTTCAATACAG | 23092 |
| rs3776241 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172277 | ACAAGCCTCACATTC[C/T]TGGATTTTATTTGGT | 23092 |
| rs3776244 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143169159 | ACACCAGTGTTCAGT[C/T]TTCAGAAACATGTGA | 23092 |
| rs3776245 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143168572 | TGGCTTTTTAACATT[A/C]TAAAACTCAAAGCAA | 23092 |
| rs3776246 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166719 | TTAAACTGTAGAATC[C/T]CCTGCCTCAAGGTCT | 23092 |
| rs3776247 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166705 | CCCCTGCCTCAAGGT[A/C]TCCAGTCCATAGATG | 23092 |
| rs3776249 | snp | A/G | 0.122411 | 0.214991 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166657 | ATGGCAGAGAATTTA[A/G]CAAAGCAGCAGGTGA | 23092 |
| rs3776250 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143166612 | TGAGGCTATGAAAGC[A/T]CTGGGGCCGTCAGGG | 23092 |
| rs3776254 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143164823 | AGGTGTGCCAAGGCC[A/G]GTGGGTTACACTGGG | 23092 |
| rs3776260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158509 | CAGAGTCCTAGGCTG[A/G]AGAGGAATTCCTGAG | 23092 |
| rs3776261 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158411 | GTTGGCTCCACCCAA[C/T]GGAGGAACAATAGGG | 23092 |
| rs3776262 | snp | A/C | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143158366 | CAACGCTCTTTGTGT[A/C]AACAGTTCGATGCCT | 23092 |
| rs3776265 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156749 | GCTCAGTTAAGCCCC[A/G]GTACTGTCATCACTG | 23092 |
| rs3776273 | snp | A/G | 0.186737 | 0.241863 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153353 | ATTTCTTCCACCAGA[A/G]ACAGTGGAAGATGGT | 23092 |
| rs3776274 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143153264 | AGAACTAAAACCTAG[C/G]GTTTCCTGCTTTCCA | 23092 |
| rs3776277 | snp | C/T | 0.11228 | 0.208646 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149081 | TAGACACCTAAAAAA[C/T]AAAAAATCCCAAGCC | 23092 |
| rs3776278 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145807 | AATCCTTAATGCCCT[A/G]GATAAAGCCCCACAG | 23092 |
| rs3776279 | snp | A/G | 0.320814 | 0.239761 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145298 | GGCTAAGTTTGCATG[A/G]CATAATTCTCAGAAT | 23092 |
| rs3776280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143380 | AGCTAAGCGACTTCA[C/T]TTTCCATATTTACCA | 23092 |
| rs3776282 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143137412 | ACTATGAACTGAAAG[A/G]GCACAGCAGGAAACT | 23092 |
| rs3776286 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136809 | AAGTGCTAGGATAAA[G/T]TTTTCTGTCTTTGTC | 23092 |
| rs3776288 | snp | C/G | 0.0763506 | 0.182913 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136622 | CTCCCACTGCCCCCC[C/G]ACAGGGTGCCTTCCA | 23092 |
| rs3776289 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136342 | CTCCTTTTGCATCCC[C/T]TGTCTACCATCTGCA | 23092 |
| rs3776290 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143136059 | TCTCCTAATCTACAC[C/T]GTACACTGATAAGTA | 23092 |
| rs3776291 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135797 | CAAAGTCCTGAAACG[C/T]TGTATATCTGTTGAC | 23092 |
| rs3776292 | snp | A/G | 0.117886 | 0.21224 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135597 | TGAAGTGCAGTAAGG[A/G]TTTTGGGATGGGGAA | 23092 |
| rs3776293 | snp | A/G | 0.25801 | 0.249872 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131012 | CCTGGGTCTCATTGT[A/G]AGCCAGGACCAGGCT | 23092 |
| rs3776294 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130616 | TCATTTTGGAAGGGA[C/T]GATTTCAAGAGAATC | 23092 |
| rs3776295 | snp | C/T | 0.279879 | 0.248208 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130371 | CTCACAAAGTAATTC[C/T]GACTTAGTCAGGAAT | 23092 |
| rs3776296 | snp | C/T | 0.258565 | 0.249853 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143130282 | ATTGTAAAACAAAAA[C/T]ATAACTCTGGGTAAC | 23092 |
| rs3776297 | snp | C/T | 0.425432 | 0.178112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128895 | GAAATTAGGTCATGA[C/T]GAAGAGCTCCTAGTC | 23092 |
| rs3776298 | snp | A/C | 0.41023 | 0.191902 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128557 | TTGTAACTGTTAAGA[A/C]GCCAAATTCAGAGGC | 23092 |
| rs3776299 | snp | C/T | 0.377187 | 0.215229 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143128086 | AGAAGCATTCTAGCT[C/T]AACACCCAAGTAAAT | 23092 |
| rs3776300 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127045 | AAAACCTTGTAATAA[A/G]TATAATTTCTGGGCT | 23092 |
| rs3776302 | snp | A/G | 0.384209 | 0.210922 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119645 | TGCAGCAGGGAGAGT[A/G]GCCTGTTTCTGGTCC | 23092 |
| rs3776303 | snp | C/T | 0.384209 | 0.210922 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119612 | ATAAAGAATATTTTA[C/T]AAACATTTTCTTAGT | 23092 |
| rs3776304 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116667 | TTCCAGATAAAGATG[A/G]TGGTGGGGATGGTGG | 23092 |
| rs3776306 | snp | C/G | 0.446249 | 0.154875 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114725 | GGGCTGGATCATGAC[C/G]TTGGAATGCATCTTC | 23092 |
| rs3776307 | snp | C/T | 0.375399 | 0.216275 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114600 | CACCCTTCTCTCTAC[C/T]ACCCTCTCAGAGAAG | 23092 |
| rs3776308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113381 | TAACTAGCAAAGTGT[C/T]CTCTGCTTCTGGGGA | 23092 |
| rs3776309 | snp | A/C | 0.338069 | 0.233974 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108579 | ATAAGTCTGAAAAAA[A/C]ACTGGGAGGCTGAAG | 23092 |
| rs3776310 | snp | A/T | 0.24134 | 0.24985 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107574 | CTAAAATGCTTTCTA[A/T]TGTGCAGGCATCACA | 23092 |
| rs3776311 | snp | C/G | 0.49947 | 0.0162704 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143107526 | TTCTGTTGAGCCAGG[C/G]AAAGCAAGATGACAG | 23092 |
| rs3776313 | snp | A/T | 0.104149 | 0.203046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143103059 | TTGTGTTTATAATCC[A/T]TATATCTTTCACAAA | 23092 |
| rs3776314 | snp | G/T | 0.277778 | 0.248452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102838 | AAAGCAAGCAAGGGA[G/T]GTGAAAAAAGTACTG | 23092 |
| rs3776315 | snp | C/G | 0.236724 | 0.249647 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102746 | AACAGAAGTTTCAAA[C/G]AGGCAGGATTGGAGT | 23092 |
| rs3776316 | snp | G/T | 0.039522 | 0.134904 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101721 | AAAAAAATTAATCCA[G/T]TTCCCAGAGAGAGGG | 23092 |
| rs3776317 | snp | C/T | 0.455621 | 0.142197 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087058 | ACATGAGTCACAATG[C/T]CAAGGACCCTGGCAA | 23092 |
| rs3776318 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086996 | ATGATCTAGCAAGCT[C/T]GTAAAACTCAGCAGA | 23092 |
| rs3776319 | snp | C/T | 0.256061 | 0.249927 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086856 | ATGGATATCTGAGTG[C/T]TGGAAGAACCAGTCA | 23092 |
| rs3776320 | snp | C/T | 0.215747 | 0.247642 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086310 | CCCCCACAGTCAAAA[C/T]TCTAGAAAAATGATC | 23092 |
| rs3776321 | snp | C/T | 0.225301 | 0.248777 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085349 | CCCCAAATTAGAGAC[C/T]CTATGCTCTGCCTCT | 23092 |
| rs3776322 | snp | G/T | 0.26818 | 0.249338 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143085136 | TCAAGAGTTTCCGGG[G/T]CCGGGACCACAATTC | 23092 |
| rs3776323 | snp | C/T | 0.225005 | 0.248747 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084581 | CCACGCTGGAGAGGG[C/T]AGAGTTCCCTGTAAG | 23092 |
| rs3776324 | snp | A/C | 0.0410537 | 0.137264 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084508 | CGCCTCCCTCCAAAT[A/C]TGTGGAAACTCAGGC | 23092 |
| rs3776325 | snp | A/G | 0.101658 | 0.201233 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077957 | GCTGGCAGCAAAGGT[A/G]AGAGGCAATCAGGGG | 23092 |
| rs3776326 | snp | A/G | 0.241627 | 0.24986 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070257 | TCATAACTAGGTAGC[A/G]TGCAAAGCAGTTTAA | 23092 |
| rs3776327 | snp | C/T | 0.307919 | 0.243198 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143067423 | AATATAGGCATGACC[C/T]TCTTTAGAGTATAGA | 23092 |
| rs3776328 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065346 | CGCAGATAACACTCA[C/T]GATGCAATTCAAAGA | 23092 |
| rs3776329 | snp | C/G | 0.329317 | 0.237084 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143065033 | ATGGACTCAGAAAAG[C/G]AAGAGATGAATCAGA | 23092 |
| rs3776330 | snp | C/T | 0.104149 | 0.203046 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062505 | ACCCAAGCTACAACA[C/T]GCTTAATTCTTGATA | 23092 |
| rs3776331 | snp | A/G | 0.431325 | 0.172108 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143062229 | ACCAGCTAAAATCTT[A/G]TAATTTAGTGCCTAT | 23092 |
| rs3776332 | snp | A/G | 0.239614 | 0.249784 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061949 | CTCAATGACTGCTCT[A/G]GACCAATGAGATGTG | 23092 |
| rs3776333 | snp | G/T | 0.25634 | 0.24992 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061900 | GATGTCTGGGAAAAG[G/T]ATCATCCTAGCCCTT | 23092 |
| rs3776334 | snp | C/T | 0.239902 | 0.249796 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143061857 | AGAGAAGAAATAATG[C/T]CTTTTCTGCTTCTGG | 23092 |
| rs3776335 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060442 | ACCCAATACTTTTTT[C/T]CCCCTCTGAATGAAT | 23092 |
| rs3776336 | snp | C/T | 0.307176 | 0.243374 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143060021 | AGTGGAATCTTAGAA[C/T]TCCTCTGGATGCCAA | 23092 |
| rs3776337 | snp | C/G | 0.308661 | 0.24302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059940 | CATTCATATCCTTCT[C/G]CACAGGGACATTTTA | 23092 |
| rs3776338 | snp | C/T | 0.438946 | 0.163706 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059875 | CTAAGAATTTGAGTC[C/T]GCTATAGTCTAATAC | 23092 |
| rs3776339 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059494 | TCAACTGTTCAAGAT[A/C]TACCTTAAGGGTTTG | 23092 |
| rs3776341 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143059074 | TAGGTTGTGTGGAAC[C/T]GGTACTCAACTGTCA | 23092 |
| rs3776342 | snp | G/T | 0 | 0 | intron-variant, downstream-variant-500B | ARHGAP26 | GRCh38.p7 | 5:143058819 | CACAAGACACTCTTG[G/T]CTTCTTGATGGAAAT | 23092 |
| rs3776343 | snp | G/T | 0.472803 | 0.113397 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054860 | GCATTCTTAACAGAA[G/T]ATGATTCATGATTCC | 23092 |
| rs3776344 | snp | A/G | 0.432504 | 0.170857 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051958 | CCCATCCTAAGACAC[A/G]TGGAGAGCTGCCATC | 23092 |
| rs3776345 | snp | A/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051922 | TGGTTCCTGGATGTG[A/T]GACAAATGTTACTGT | 23092 |
| rs3776346 | snp | A/G | 0.499609 | 0.0139722 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051628 | TCATTTAAAATCCAA[A/G]CTAAGTTGAATACAG | 23092 |
| rs3776347 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143051501 | ATATGCCACAGAGAC[A/G]TCATTTACACTCTTC | 23092 |
| rs3776349 | snp | C/T | 0.246769 | 0.249979 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050635 | TCCTATGTAAGCCTT[C/T]AGGTCTTAGAAATCA | 23092 |
| rs3776350 | snp | C/T | 0.213333 | 0.247296 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050047 | GCAACCCCCCAACCC[C/T]ACTCCAGCAAACACA | 23092 |
| rs3776352 | snp | A/G | 0.428635 | 0.174898 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143042402 | AAGTGACAGGTATTC[A/G]GTTGAAATCTAGAAG | 23092 |
| rs3776354 | snp | C/T | 0.165527 | 0.235296 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143041450 | AAATGCCAAAAATGA[C/T]ATTAAAAATTCATAC | 23092 |
| rs3776359 | snp | A/G | 0.287085 | 0.247234 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143029213 | ATTTAATCAATTTCA[A/G]CACCCTTAAAAGCCA | 23092 |
| rs3776362 | snp | G/T | 0.230017 | 0.2492 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143019292 | GACTGACACTGGCAG[G/T]GACCACTTCCTCAAA | 23092 |
| rs3776364 | snp | A/C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143017133 | TAGAAAAGAAAATGC[A/C/T]GGACATTTGGAATTT | 23092 |
| rs3776365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016967 | AGAGCATTAGCGCCA[C/T]CTGTGGTAGATGAGC | 23092 |
| rs3776366 | snp | A/C | 0.232359 | 0.249377 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008637 | ATAAAGATGCTGGGG[A/C]AATAGGTTCATAAGG | 23092 |
| rs3776367 | snp | A/T | 0.0341408 | 0.126114 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008267 | TTGGCTAACATGCAC[A/T]TCAGTTATCATCCCT | 23092 |
| rs3776368 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143005933 | TGTACCTGTTGGTGC[C/T]GAGTCCCTTCCCCTA | 23092 |
| rs3776369 | snp | C/T | 0.495596 | 0.0467178 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003544 | ATCTCCAATCAAGGT[C/T]AATTTTACATTTCTA | 23092 |
| rs3776370 | snp | A/G | 0.231189 | 0.249291 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003438 | CTCATTAAAGGACAA[A/G]GGGCTTAAGGATGCG | 23092 |
| rs3776371 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982959 | GATGCAAGGCTGCAT[G/T]TGCTATCAGAGGTGG | 23092 |
| rs3776372 | snp | C/T | 0.205417 | 0.245993 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982454 | GTCCAAACAGTAGGA[C/T]AAGACACCCTCCCAC | 23092 |
| rs3776373 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142982091 | ACATTTGGTCACAGG[A/G]CTTTTCAGCCTTCAA | 23092 |
| rs3776376 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142976064 | GAGTGAGAATTTCTC[A/G]TGAAAAGCCCTTAAG | 23092 |
| rs3776383 | snp | G/T | 0.0267878 | 0.112589 | intron-variant, nc-transcript-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142966195 | ACGTTATAAATGCGA[G/T]TAGGAGAGTTTTCCT | 23092 |
| rs3776390 | snp | C/T | 0.251859 | 0.249993 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142954003 | TTTAAAATGGGGAAA[C/T]TTGTCCCTTGGTGGT | 23092 |
| rs3776395 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934585 | CATTAGGGAGATGGT[C/G]ATTAAAGCTGGAGCT | 23092 |
| rs3776396 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142934303 | ACATTCTGGAGCAAG[A/G]AGATGTTTCTTTCAA | 23092 |
| rs3776398 | snp | A/G | 0.299916 | 0.244966 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929730 | TGAGATTTCCACCCC[A/G]AGCCACAGAGGAAGT | 23092 |
| rs3776400 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926120 | CCACTGGCTATACCA[A/T]CTCATAGCCTCCTCA | 23092 |
| rs3776403 | snp | A/C | 0.242201 | 0.249878 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925823 | TGGCAAGAGTTCATT[A/C]CCCAGCTTCCATCCA | 23092 |
| rs3776404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925478 | TCTTGGAGAATGACA[C/T]CTTTTCCATGTCTGT | 23092 |
| rs3776405 | snp | C/G | 0.257176 | 0.249897 | intron-variant, missense | ARHGAP26 | GRCh38.p7 | 5:142919281 | CTTGTAGGTGCATCA[C/G]CTCGACTTCTGCCTT | 23092 |
| rs3776408 | snp | C/T | 0.239614 | 0.249784 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914164 | AGTCTCAGGATGCCA[C/T]AGAGCCAGGGAAAGG | 23092 |
| rs3776409 | snp | C/T | 0.251578 | 0.249995 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907309 | AAAGCCTCCTCCAAG[C/T]GCTTGTGACCATTCC | 23092 |
| rs3797074 | snp | A/G | 0.267636 | 0.249377 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127606 | GCGAGGTTGCTTAGG[A/G]TTTAGTGCTTAGTCC | 23092 |
| rs3797075 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143117367 | ACAGAAAGGCCTAGA[C/T]GTCAGCCTCTGCAGG | 23092 |
| rs3797076 | snp | A/G | 0.253544 | 0.249975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102550 | ACTTTTAATTGTGTG[A/G]CCGGCATGGGTCCAG | 23092 |
| rs3797080 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922992 | GCAATTCAGAAACTA[C/T]GGTATCGTCTCCCAA | 23092 |
| rs3797081 | snp | C/T | 0.259951 | 0.249802 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922795 | TGAAACCAGGAAAAA[C/T]GGATTCATGTGTTGC | 23092 |
| rs3797088 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818060 | CATGTCATCCAGTCC[C/T]AACACCAGGAATGTA | 23092 |
| rs3815199 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120779 | GCTATTTCAGGATAT[A/G]ACACGCTTTATCATT | 23092 |
| rs3822382 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143157332 | AAAATTAGCTGGATG[C/T]GGAGGTGTGCACCTG | 23092 |
| rs3822384 | snp | A/G | 0.360632 | 0.224189 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143141021 | GGATCTGCAAAGGCA[A/G]CCTGAGAAAGGGCAC | 23092 |
| rs3822385 | snp | C/T | 0.470618 | 0.117591 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143127899 | AGTACCAATGACTAT[C/T]TCAACATAGTGAAGC | 23092 |
| rs3822387 | snp | C/T | 0.4444 | 0.15719 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143108740 | ACTGATAAAGAAGCA[C/T]ACACTCATGAAATAC | 23092 |
| rs3822388 | snp | C/G | 0.458833 | 0.15347 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143084764 | GCCACCGCGCCCAGC[C/G]GAGAAAGTATTTCTA | 23092 |
| rs3822389 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143079906 | AGAGGGAGAAGACCA[C/T]GTGAGGCAACATGAG | 23092 |
| rs3822390 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143077567 | GAGCCTTTTATGAGT[C/T]CTGTCTGCTGCTGCT | 23092 |
| rs3822391 | snp | A/C | 0.214541 | 0.247473 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143074380 | AAAAAGGCCAGGATA[A/C]CAGACAGACTGAAAT | 23092 |
| rs3822392 | snp | C/G | 0.424037 | 0.179474 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143070311 | GGTTAGGGCTGGGGA[C/G]AATGACCTTGTAGGA | 23092 |
| rs3822393 | snp | C/G | 0.430136 | 0.173352 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066849 | TCTTTCTCCCAGCTG[C/G]CCCTGTGCTGGCTCA | 23092 |
| rs3822394 | snp | G/T | 0.427879 | 0.175668 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143050246 | AAAAGGGACACAAAT[G/T]TTTAACAGCACAGAA | 23092 |
| rs3822396 | snp | C/T | 0.187053 | 0.241946 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023292 | ACAGAGCAATGGTAA[C/T]GATGTCCCTCCCCAT | 23092 |
| rs3822397 | snp | C/T | 0.475348 | 0.108251 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143013997 | CCATTATCTTCCTCA[C/T]TTTCCCTAGTTTGCA | 23092 |
| rs3822398 | snp | A/G | 0.474091 | 0.11083 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143008396 | CCTCTGCATGACAAA[A/G]TGGGTCCACCATCAC | 23092 |
| rs3822399 | snp | A/G | 0.230896 | 0.249269 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143002481 | TGCCGTTTTCATGGT[A/G]AGAGGAGAGACCACC | 23092 |
| rs3822400 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142973848 | CGCCCTCCCACCCAC[C/T]TCCCCCTAAACCAAC | 23092 |
| rs3822403 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142921438 | CTCTAGTCTCTTACA[C/T]AATAGTTTACCATGG | 23092 |
| rs3834247 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143064479 | CCATAAATAGGCCAG[-/G]AAGCGGTATCACTCA | 23092 |
| rs3836769 | in-del | -/T | 0.236505 | 0.249635 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208187 | AGAGCTCTTTTTTTT[-/T]CCCAAAGAGCACAAG | 23092 |
| rs3836770 | snp | A/C | 0.292523 | 0.246357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184348 | TTATACATGTTTTTA[A/C]GGGAGAGACAAAAGG | 23092 |
| rs3836771 | in-del | -/TAA | 0.122411 | 0.214991 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143144398 | taataataataataa[-/TAA]agaaaaaatGATCCC | 23092 |
| rs3836772 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143143078 | AAAAAGAAGAGGCAA[-/A]GAGGACTGTTCTTTA | 23092 |
| rs3836773 | in-del | -/T | 0.472147 | 0.114677 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143131871 | CCCTACTGTTTATTT[-/T]GGCCATCCCCTGGTG | 23092 |
| rs3836774 | in-del | -/AT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143087070 | CCCCTGATAACACAC[-/AT]GAGTCACAATGCCAA | 23092 |
| rs3836775 | in-del | -/TT | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025968 | ATACAAAGGCATCTA[-/TT]TTTTTTTTTCATTGT | 23092 |
| rs3836776 | in-del | -/T | 0.498133 | 0.030494 | intron-variant | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142964589 | AACATCGGTTTTTTT[-/T]GCTGCTGTTGTTGTT | 23092 |
| rs3836777 | in-del | -/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929646 | AAGTCAACAGGATTT[-/G]TTTTCATTCCAAGAA | 23092 |
| rs3836778 | in-del | -/AC | 0.493837 | 0.055168 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142922422 | CACACACACACACAC[-/AC]TCTTCTGTCAATGTA | 23092 |
| rs3839208 | in-del | -/A/AA | 0.665178 | 0.0227138 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142923087 | AAGAAAAAAAAAAAA[-/A/AA]CTCCATGACAAGTTC | 23092 |
| rs3850572 | snp | A/C | 0.24019 | 0.249807 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142897458 | TCACTGTATGAATAC[A/C]TTCTCCCCATCCCCA | 23092 |
| rs3893579 | snp | C/T | 0.430136 | 0.173352 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066776 | ATGCACACAAACTGC[C/T]AAGCAAACACAAGCA | 23092 |
| rs3996405 | in-del | -/CCTT | 0.444267 | 0.157354 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143045430 | CCAGGGCTCTAGACC[-/CCTT]TGAAGGGGGAGCTTC | 23092 |
| rs4376299 | snp | C/T | 0.498673 | 0.0257246 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142986192 | tgactttttaatgat[C/T]gccattctaactggt | 23092 |
| rs4637583 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988188 | ttattggtctattca[A/G]ggattcaacttcttc | 23092 |
| rs4912647 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142987092 | accttgggcggtatg[A/G]ccattttcacgatat | 23092 |
| rs4912649 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143101559 | CCTCTCCTTTCCTTA[A/G]CATCCAACCAGGCAG | 23092 |
| rs4912878 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794348 | GATGATTTCCCAGAG[C/G]AATACTGGGGTGCTA | 23092 |
| rs4912882 | snp | A/G | 0.302184 | 0.244493 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142866483 | CTTGGTAGGTACAGT[A/G]TTCAGTAAGTTAATG | 23092 |
| rs4912886 | snp | A/C | 0.081446 | 0.184634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142925346 | CTGCAAAAGAAAAAA[A/C]CAAGAGCAACATAAG | 23092 |
| rs4912887 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000663 | ctggataaagaaaat[A/G]gggcacatatacacc | 23092 |
| rs4912888 | snp | A/G | 0.474091 | 0.11083 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007538 | GTTAATTGGCAGGCT[A/G]TTTTTCCTCTGGAAA | 23092 |
| rs4912889 | snp | A/G | 0.491732 | 0.0637633 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143007679 | AGTTAATTAACCCAT[A/G]TGATGCTATGAAATA | 23092 |
| rs4912890 | snp | A/G | 0.3752 | 0.216391 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022273 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 23092 |
| rs4912891 | snp | C/T | 0.437401 | 0.165472 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143022552 | CAGTAAAACTTTGTT[C/T]TACAAAACAGGCAAT | 23092 |
| rs4912892 | snp | A/C | 0.411914 | 0.190483 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143046673 | TATTAAGTAAAGATA[A/C]ATCTTTCCAAATTTT | 23092 |
| rs4912893 | snp | C/T | 0.41141 | 0.19091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048241 | TTGTCTTAAACTTTA[C/T]GGTGCATTTGTTTTT | 23092 |
| rs4912895 | snp | A/G | 0.422315 | 0.181128 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111572 | TTAGTTGCTGTTACT[A/G]TTGATGGAAATCCTA | 23092 |
| rs4912896 | snp | A/G | 0.44333 | 0.158505 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143112506 | TTTACTACCTTGACT[A/G]TTTTTAAGTGTACAG | 23092 |
| rs4912898 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143113358 | CATCTGAAATGTAGC[C/T]ATGTGTTTCCCCAGA | 23092 |
| rs4912900 | snp | A/G | 0.329317 | 0.237084 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143184990 | AGAGGTCTATGCAAC[A/G]GTGAGTGGATTTTTA | 23092 |
| rs4912902 | snp | A/G | 0.178144 | 0.239451 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205734 | GAGAAGCCTCAGCTT[A/G]GCCCAGGTTTCCACA | 23092 |
| rs5871828 | in-del | -/C | 0.422787 | 0.180679 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142822239 | GGCAGTTTAGTCTTA[-/C]ATTTGCTCAGAGTGC | 23092 |
| rs5871829 | in-del | -/C | 0.444133 | 0.157519 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142907952 | TTTTATATAGTAGTT[-/C]CAGGAAGCCTAAGAG | 23092 |
| rs5871831 | in-del | -/A | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991662 | TGTTTAGATACAGAA[-/A]TACTATTGTGTGTCA | 23092 |
| rs5871832 | in-del | -/T | 0.0205511 | 0.0992634 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992058 | TTAGGACTTTTTTTT[-/T]GTTTTTGAATATTCC | 23092 |
| rs5871833 | in-del | -/A/AA/AAA | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143016702 | TGAGACTCTGTCTCA[-/A/AA/AAA]AAAAAAAAAAAAAAA | 23092 |
| rs5871835 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116002 | ATAAAAATAGAATCG[-/A]ACAGGATAAGATGGG | 23092 |
| rs5871836 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143116022 | ATAAGATGGGAATAG[-/A]AAATATCAGAGTGTG | 23092 |
| rs5871838 | in-del | -/C | 0.021333 | 0.101051 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143187812 | CATGTCATAAGTGCA[-/C]TCTATCCATTGGGAG | 23092 |
| rs6149273 | snp | C/T | 0.277778 | 0.248452 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012552 | ttatatacatacata[C/T]atatatatatatata | 23092 |
| rs6149274 | in-del | -/A | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143167483 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 23092 |
| rs6580259 | snp | C/T | 0.19646 | 0.2442 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781769 | CAGGCTGGAGTGCAG[C/T]GGTATTATCTTGGCT | 23092 |
| rs6580260 | snp | G/T | 0.373598 | 0.21731 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884841 | CCAAGAAGTGTTTTT[G/T]GGACAGTATTAAGGC | 23092 |
| rs6580261 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895952 | TCCTTAAAGTCGTCA[A/G]TTACTTCAGTCTCCA | 23092 |
| rs6580262 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895977 | TCTCCATATATGAAT[A/G]TTAAAACCTTAGACC | 23092 |
| rs6580263 | snp | C/T | 0.244776 | 0.249945 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896281 | CTAATAATCTTTATA[C/T]ATACTTCGATTAATA | 23092 |
| rs6580264 | snp | A/G | 0.235564 | 0.249583 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142999770 | acaaaaacatgaaaa[A/G]aaattgacttgattt | 23092 |
| rs6580265 | snp | A/C | 0.41441 | 0.188333 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143054162 | TAAACGTTTTTAAGA[A/C]TTTGATACATATTAC | 23092 |
| rs6580266 | snp | A/G | 0.433382 | 0.169915 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056183 | ATTACCTAACCCTTC[A/G]TATTCTGCACATAAA | 23092 |
| rs6580267 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088416 | AGAATGGTTAAATAT[A/G]TTGTTCTGAGATGCC | 23092 |
| rs6580268 | snp | A/G | 0.25634 | 0.24992 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094952 | aaaagtagaaggcaa[A/G]gaattgaacatactg | 23092 |
| rs6580269 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095060 | GTGAAAGGAAATTGT[A/G]CCATATCACCTGGAC | 23092 |
| rs6580270 | snp | A/G | 0.267091 | 0.249415 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099024 | AAAGACACAATGCTG[A/G]AAAAAGGTCACAAAG | 23092 |
| rs6580271 | snp | A/G | 0.387074 | 0.209071 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119762 | CCACCTTTAGAGGAG[A/G]AAGTTAAACTCAGCC | 23092 |
| rs6580273 | snp | C/T | 0.499879 | 0.0077866 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138752 | ATATAACTTACCAGG[C/T]GGTTTCTTGTGTTGG | 23092 |
| rs6580274 | snp | G/T | 0.367091 | 0.220884 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143140305 | CACCCTGGCATGGTG[G/T]TTGAAAGTGGAGGCT | 23092 |
| rs6859305 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884635 | GCTTATTGGATGTTC[C/T]GTACTTTAATTATGC | 23092 |
| rs6860650 | snp | A/G | 0.476918 | 0.104919 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142775570 | tgttgtataattact[A/G]tctctttcgagaaca | 23092 |
| rs6860667 | snp | A/G | 0.205417 | 0.245993 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203839 | agaaaaccaaacacc[A/G]catgttctcactcat | 23092 |
| rs6860834 | snp | A/G | 0.204803 | 0.245881 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203908 | gaacatcacacaccg[A/G]ggcctgtcagggggt | 23092 |
| rs6861366 | snp | A/G | 0.354019 | 0.227333 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143194701 | AATGATTTTCCTTCA[A/G]TTTGTTTTTATTCAC | 23092 |
| rs6861836 | snp | C/G | 0.376195 | 0.215812 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142778500 | tgtgttttgcttttc[C/G]agttgatcatttgtc | 23092 |
| rs6863309 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854092 | AATTATTATGTTTTT[A/G]AAAGCttgtcacaca | 23092 |
| rs6864329 | snp | C/G | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209500 | AAATAGTCAAGGCAg[C/G]ccgggcacagtggtt | 23092 |
| rs6864372 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009078 | GAGCTACTCTCCCCC[A/C]CTGGTGTTTATCGTC | 23092 |
| rs6864475 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143148366 | TGTGAGATATTTACA[A/G]ATCTGCAAAATGAGT | 23092 |
| rs6864595 | snp | A/G | 0.119281 | 0.213102 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151939 | ccagcctgggctacc[A/G]agcaagactccatct | 23092 |
| rs6864988 | snp | C/T | 0.338523 | 0.233803 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143200201 | ATGTTGGTGGGGTAA[C/T]GGTGAGAAGGAATTG | 23092 |
| rs6866262 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142776229 | cctcccgtcttggcc[C/T]cccaaagtgctgcga | 23092 |
| rs6866914 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143100580 | GCTTAATCACCTCCC[A/G]TGGTGTGAATTTGGG | 23092 |
| rs6867173 | snp | C/G | 0.175897 | 0.238765 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143180448 | CCAGTTGATCTTGTC[C/G]CTTTCTGTAGTTCCA | 23092 |
| rs6867976 | snp | C/G | 0.174288 | 0.23826 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142786230 | caagtgatcctcctg[C/G]cttggcctcccaaag | 23092 |
| rs6868027 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854554 | ATTGCCAGAATAAAT[A/G]TATGACACTGTTATA | 23092 |
| rs6869553 | snp | G/T | 0.305685 | 0.24372 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143098379 | ATTTTGTTATATTTT[G/T]TACAAGTATGTTACT | 23092 |
| rs6870173 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083087 | CGAAGGCAGTCTCTA[G/T]GTATCTTGGGGAAGC | 23092 |
| rs6870362 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142879900 | TAaaaggaggcagct[A/G]gtacttaggtttagc | 23092 |
| rs6870936 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988429 | aagttttttgatctt[C/T]tcaaaaaactagctg | 23092 |
| rs6872015 | snp | G/T | 0.030665 | 0.119967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895257 | tttctttgagacagc[G/T]tctcgctctgtcacc | 23092 |
| rs6872174 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142895323 | gcagcctctgccttc[C/T]gggttcaagcgattc | 23092 |
| rs6872438 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787255 | TTATCATTGGGGTGG[A/G]AGAGTGCCATTAAAA | 23092 |
| rs6872618 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142898013 | CTATGCAAATCGACC[A/G]TGTTCATTTGTTTCT | 23092 |
| rs6872858 | snp | C/T | 0.275464 | 0.2487 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142854865 | CTTTGTATTTTTGTT[C/T]CATTGCAAACTGTTT | 23092 |
| rs6873805 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102241 | CTCCCTCTTCTCTTC[A/G]CTTCCTGCCTTCCAG | 23092 |
| rs6874495 | snp | C/G | 0.1652 | 0.235179 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863079 | TAGAGCTACGGAAAG[C/G]GGTTGGCTCCTTGGT | 23092 |
| rs6874763 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142842761 | tccctcaacatttca[C/T]ttggaggaggattat | 23092 |
| rs6874920 | snp | C/T | 0.264906 | 0.249555 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143089493 | tttgttatacttcca[C/T]caggggtggtggtgt | 23092 |
| rs6875031 | snp | G/T | 0.214843 | 0.247516 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142863350 | CTGACCTCGTGATCC[G/T]CCCACCTCGGCCTCC | 23092 |
| rs6875182 | snp | A/G | 0.258843 | 0.249844 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142884008 | CTTCTTTATTTGGCC[A/G]GAAAATATTTTTTCT | 23092 |
| rs6875280 | snp | A/G | 0.313814 | 0.241719 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143099384 | accatgtgagaatga[A/G]ggtgagacatgggga | 23092 |
| rs6876462 | snp | C/T | 0.424193 | 0.179323 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143129416 | AAGGTCAGAGAGTTA[C/T]ATAATTTGCCCAAGG | 23092 |
| rs6877111 | snp | C/T | 0.234982 | 0.249549 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142998685 | GCTGTGATCGAGCCA[C/T]TGCCCTACAGCCTGG | 23092 |
| rs6877124 | snp | A/G | 0.141596 | 0.225274 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871934 | AGAGCGCTTTGGACA[A/G]ACCGCAGCTATCTCG | 23092 |
| rs6879799 | snp | G/T | 0.0966517 | 0.197444 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142806039 | TTATATAATGCAAAG[G/T]TGTGTGTCTTATTCT | 23092 |
| rs6882666 | snp | C/G | 0.295854 | 0.245759 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143094663 | caagggaggggaaag[C/G]cttcttatccctgac | 23092 |
| rs6883314 | snp | G/T | 0.288906 | 0.246954 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142841895 | CACATGTTCATTGTG[G/T]CTACCTCTCCCCACC | 23092 |
| rs6884086 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170865 | AAAGAGACTGAAGCA[C/G]CCCAGTCATGTTTCT | 23092 |
| rs6884099 | snp | A/G | 0.203267 | 0.245593 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142877265 | GTTCAGTTAAGCTCA[A/G]CAAGCAAAGCCGCAC | 23092 |
| rs6884972 | snp | A/G | 0.432944 | 0.170387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988484 | gttttttgtgtctct[A/G]tctcctccagttctg | 23092 |
| rs6886059 | snp | A/G | 0.313082 | 0.241911 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142888049 | CTAACCACATCAATA[A/G]CAACTATAATATAGG | 23092 |
| rs6886180 | snp | C/T | 0.432944 | 0.170387 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142988491 | gtgtctctgtctcct[C/T]cagttctgctctgat | 23092 |
| rs6886315 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209638 | atacaaaaattagcc[A/G]ggcatggtggtgggc | 23092 |
| rs6886351 | snp | A/G | 0.267364 | 0.249396 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142886004 | TTTAAAAAGTAGTTC[A/G]CTTGGAAAGAAAAAT | 23092 |
| rs6887217 | snp | A/G | 0.337158 | 0.234315 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142882729 | ACCCTGCCAAGCACT[A/G]TATGTGGTTTATTTC | 23092 |
| rs6887887 | snp | A/G | 0.172997 | 0.237846 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143156348 | TTAGGGATCTGGAAA[A/G]CCAGGCAGGATCAAC | 23092 |
| rs6888136 | snp | A/T | 0.241914 | 0.249869 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142985523 | ttatcttttTTTTTT[A/T]AAtttaagttctagg | 23092 |
| rs6888245 | snp | C/T | 0.496382 | 0.0423778 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143159394 | GCTATCAATAAAGGA[C/T]GGCCTAAATAAATAG | 23092 |
| rs6888562 | snp | A/C | 0.235564 | 0.249583 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142991953 | GAGTTGCATATGGGA[A/C]TATCCATTTCCCTGA | 23092 |
| rs6889060 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143205230 | CGCTTCTTGTCAAAT[A/G]TATTTTAAGCTCTTG | 23092 |
| rs6889083 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142855474 | CAGGTGCTTTGCTCC[C/G/T]TAGATATCCATCCAC | 23092 |
| rs6889140 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142818159 | GGCCTGGAAGTGTAT[C/T]TTTCCTTCCACCGTG | 23092 |
| rs6889385 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142930927 | GGCTTGGGTGCATAT[A/G]GGGCCCAGGCTTGTG | 23092 |
| rs6889669 | snp | C/T | 0.178785 | 0.239642 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788358 | GCTTCCCGACTCCCA[C/T]CCCATTTTTTTGTTG | 23092 |
| rs6889971 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142958936 | AAAAAAAAAAAGAAA[A/G]GAAAATATATAGAGG | 23092 |
| rs6890293 | snp | A/G | 0.127599 | 0.217986 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773979 | CGTGGGCATTTTGCA[A/G]TACATAAGCGCTTCT | 23092 |
| rs6890829 | snp | G/T | 0.499673 | 0.0127754 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209717 | ACCTGGGAGGCAAAG[G/T]TTGCAGTGAGCCAAG | 23092 |
| rs6891320 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226916 | GTGTGCCATACCTGC[A/G]GCTCAAAGGGAAGGC | 23092 |
| rs6892654 | snp | A/G | 0.24449 | 0.249939 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142889491 | GATGTGGTGGCACGC[A/G]CCTGTAATCCCAGCT | 23092 |
| rs6892897 | snp | C/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143066512 | acaccttccataaat[C/G]ttaattTCTACAATC | 23092 |
| rs6893558 | snp | A/G | 0.107341 | 0.205301 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142846816 | TCATTCATTAATTCA[A/G]TATGTATTGATTAGT | 23092 |
| rs6893890 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143150134 | TTTAAATCTTTGGCA[G/T]GTCCTCAGCTTGACT | 23092 |
| rs6894433 | snp | C/T | 0.339429 | 0.233457 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142773786 | AATGATTATCAGTGA[C/T]TGTCTTTTCACTGAG | 23092 |
| rs6894946 | snp | A/G | 0.451483 | 0.148002 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176167 | ACGTGACAATGAAAC[A/G]GAATTGTCTTTATGA | 23092 |
| rs6895485 | snp | C/T | 0.0700422 | 0.173537 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143223267 | TTTTTTGAATGGTTT[C/T]CTAACAACTTGAAGC | 23092 |
| rs6896055 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143135899 | CTCACTGTGGTCTGC[A/C]CGTGGCCTGGGCCCC | 23092 |
| rs6896092 | snp | A/G | 0.38286 | 0.211774 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142872242 | CGATCCCTAACCTCA[A/G]GGGACAAATCTGGGA | 23092 |
| rs6896777 | snp | C/G | 0.030278 | 0.119257 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143145143 | GGAGAAAAATAATCT[C/G]CTGGTAACATTTTAG | 23092 |
| rs6896779 | snp | C/T | 0.141258 | 0.225111 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142871937 | GCGCTTTGGACAAAC[C/T]GCAGCTATCTCGGGA | 23092 |
| rs6896844 | snp | C/T | 0.452227 | 0.146984 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035135 | TAAGCAATAAGTATG[C/T]ATGTAAGTATAGGAA | 23092 |
| rs6896864 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142984696 | ccataagattataat[A/G]gagctaaaaaattcc | 23092 |
| rs6897891 | snp | A/G | 0.232651 | 0.249397 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160952 | GTTAACTGAGCTCTC[A/G]CTCAGGAAGCTGAGT | 23092 |
| rs6897991 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143078439 | AGACCTGAGTGTGTC[C/T]GTTTTATTCCCTCGG | 23092 |
| rs6898278 | snp | A/G | 0.450985 | 0.148678 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143093994 | gttcaacgccccccc[A/G]tggggatttctcccc | 23092 |
| rs6898336 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142832027 | TCTTCCCTTGGCTCC[C/T]TGTTGTCTATTATGA | 23092 |
| rs6898510 | snp | C/T | 0.237593 | 0.249692 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992870 | GACTGCTTAACCTTC[C/T]TGGGGTGAGCACAAC | 23092 |
| rs6898520 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143160640 | ccaggcatgtgccac[C/T]atacccagctaattt | 23092 |
| rs6898675 | snp | C/T | 0.33875 | 0.233717 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142772094 | TTAGCAGAGTAGAGT[C/T]GTAGCTGTGGGAATT | 23092 |
| rs7442669 | snp | A/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151291 | gctggctaggatgtg[A/G]agcagtgggaactct | 23092 |
| rs7442887 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151307 | agcagtgggaactct[C/T]actcattactggtgg | 23092 |
| rs7442889 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151309 | cagtgggaactctca[C/T]tcattactggtggga | 23092 |
| rs7446432 | snp | A/C | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151315 | gaactctcactcatt[A/C]ctggtgggaatacaa | 23092 |
| rs7446668 | snp | A/G | 0.465368 | 0.126951 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020831 | GTTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 23092 |
| rs7447182 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143151270 | agaacactgacaaca[C/T]caaatgctggctagg | 23092 |
| rs7449036 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142997800 | gtgattttgctaaag[G/T]ggtccccagatgtaa | 23092 |
| rs7449125 | snp | C/G | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143203241 | gaaaaaaaaacaacc[C/G]catcaaaaagtgggt | 23092 |
| rs7700356 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176306 | AGACTTGCCAGCCAC[G/T]TCTGCTTTTATATTT | 23092 |
| rs7700697 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176724 | GCTTAACGTAAACCT[A/G]AGTAGCAGACCATTA | 23092 |
| rs7700732 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176783 | TTAAATTTCAATACT[A/C/G]TAATGAAAATTTCCA | 23092 |
| rs7702357 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143035679 | ggtggctcacgcctg[C/T]aatcccagcattttg | 23092 |
| rs7703874 | snp | A/G | 0.26271 | 0.249677 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143124684 | CTTAGGCCTGGAGCA[A/G]AGTATCATTTCTGTC | 23092 |
| rs7703925 | snp | A/G | 0.118584 | 0.212673 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142823814 | TGGTTATTTAAAGGC[A/G]GTCTTTCCTTAGGCT | 23092 |
| rs7704117 | snp | A/C | 0.166506 | 0.235645 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182509 | CTCTGATGCTTCCTA[A/C]ATATTTGTTAAGTGA | 23092 |
| rs7704255 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793908 | GTTTTAATAAGTTAC[A/G]TTTGTAGAGGCGGTG | 23092 |
| rs7705006 | snp | G/T | 0.439502 | 0.163061 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121602 | TGTTGCAAATATTTT[G/T]ACCTATAGTTTGTCT | 23092 |
| rs7705013 | snp | A/G | 0.47852 | 0.101384 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143121622 | ATAGTTTGTCTTTCA[A/G]TTTTATAAATGGTGT | 23092 |
| rs7705069 | snp | A/T | 0.312348 | 0.242101 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143183101 | AAAAAAGAAAAAAAA[A/T]CCTCATTTCCTTTCC | 23092 |
| rs7705435 | snp | A/C | 0.491104 | 0.0660973 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143213413 | TCATGCACCTTGTCT[A/C]TTCCCTCCCCTGGGG | 23092 |
| rs7705560 | snp | A/G | 0.477345 | 0.103991 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142908962 | TCTCTTTGCTCCTAT[A/G]CTTTATTTTCTTCCT | 23092 |
| rs7705859 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143142741 | TTTCCCAGAGATGGT[A/T]AACTCAGAAATTGCT | 23092 |
| rs7705923 | snp | A/G | 0.427271 | 0.176281 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143024896 | TGAAATCCCAGCCTC[A/G]AGAATTACTGAGTGT | 23092 |
| rs7706243 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142820827 | TTTTCTTATTTTTCC[C/T]GGAACATTATGAAGT | 23092 |
| rs7707272 | snp | A/G | 0.498133 | 0.030494 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052054 | AGGGAGTGCAAGATG[A/G]CAAAGACACAAATTA | 23092 |
| rs7708015 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793708 | ttcttgtgcctcagc[C/T]tctcgagtagctggg | 23092 |
| rs7709171 | snp | C/T | 0.401316 | 0.199006 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143110228 | attttctttgcttat[C/T]gcctgtcctactcca | 23092 |
| rs7709508 | snp | A/G | 0.393065 | 0.205018 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143118547 | aggccaagctgggag[A/G]atcacttgagaccag | 23092 |
| rs7710416 | snp | C/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142916893 | CTCACTACAACCCAG[C/G]GGGGTAGGTCCTCCA | 23092 |
| rs7710429 | snp | A/G | 0.309401 | 0.24284 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143096288 | ttaaaaagtcattaa[A/G]tattgggaagttgtc | 23092 |
| rs7710883 | snp | A/C | 0.188946 | 0.24243 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788411 | ACAAAGAGAAGATAC[A/C]TTACCAGAGTGTCAC | 23092 |
| rs7711483 | snp | A/G/T | 0.332344 | 0.27946 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012577 | tatatatatatatat[A/G/T]ATGATCAGGTTCACC | 23092 |
| rs7712624 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142992845 | TGGGTTCTGTGCCTC[A/G]CCTGATGCGGACTGC | 23092 |
| rs7714015 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088763 | tttatccctgacata[C/T]gtgatccctgccgct | 23092 |
| rs7714397 | snp | C/T | 0.105569 | 0.204058 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788172 | tgcccagcttatttt[C/T]gtatttttagtagag | 23092 |
| rs7714494 | snp | C/T | 0.474992 | 0.108989 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176278 | CCATCTGCTGCTCAG[C/T]AGACTGCATAAGAGA | 23092 |
| rs7714781 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143025522 | AAAACCACCGGGCCT[C/T]AAGGCAGAAGGGAAT | 23092 |
| rs7715088 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143119793 | CTAAAAAAATTATAG[A/G]AAAGTACACATCTGC | 23092 |
| rs7716396 | snp | A/T | 0.180383 | 0.240111 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143202270 | aacccctgctttttt[A/T]tttttccatttgctt | 23092 |
| rs7716692 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172346 | AATGAGAATAAAAAA[A/T]AAGATTAACAAAGGC | 23092 |
| rs7717491 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143023747 | GGCCTGGCCGCCTAT[A/G]CACTGGCCCACGAGG | 23092 |
| rs7717765 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176716 | AGTTAAGGGCTTAAC[A/G]TAAACCTAAGTAGCA | 23092 |
| rs7719923 | snp | C/T | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120280 | ATTCAAAAATATGCC[C/T]ACGTCTTTAGCAAAT | 23092 |
| rs7720631 | snp | A/G | 0.31503 | 0.241394 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143012493 | GGGGTTAAATAAGTG[A/G]TTCTCAACTGAGAGT | 23092 |
| rs7720812 | snp | G/T | 0.0637235 | 0.166737 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143218355 | TGCCgagcaaaatct[G/T]gtctgcttgttctgt | 23092 |
| rs7720909 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143186093 | ACCCTCAAGAAAGCC[A/G]TTCTCAGAAGCCTAA | 23092 |
| rs7721397 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142793964 | ATTTTCCATGGTGag[A/G]gagagaagaaccaat | 23092 |
| rs7721566 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142794067 | acctgccagactctc[A/G]tgactccaaaggata | 23092 |
| rs7721710 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143182829 | AGCCCCATGTAAATA[A/G]TCATCTCCATAAATC | 23092 |
| rs7721749 | snp | A/G | 0.319136 | 0.24025 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020554 | AGAAGAAGAAAAAAT[A/G]TAACACTTCCTCCTC | 23092 |
| rs7721863 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143138567 | ATTCTGGCCCAATAG[A/G]TAGGAACGGTGGTCT | 23092 |
| rs7721905 | snp | A/G | 0.474813 | 0.109357 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143000061 | ctataataagatact[A/G]ctacgcatacccatt | 23092 |
| rs7723074 | snp | A/T | 0.283421 | 0.247756 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086358 | CATCTTTATTTTTAG[A/T]GTCTTATACAAGCAA | 23092 |
| rs7723103 | snp | C/T | 0.375 | 0.216506 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143095196 | acatatatacacagt[C/T]acatacaATTttttt | 23092 |
| rs7723139 | snp | C/G | 0.246769 | 0.249979 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142912305 | GTGAAAAAAGCCAGA[C/G]AAAAAGAGCACATAC | 23092 |
| rs7723212 | snp | A/G | 0.441021 | 0.161279 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142781873 | CGTGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 23092 |
| rs7723229 | snp | A/G | 0.187053 | 0.241946 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142957518 | GTCTTTGTACCATTG[A/G]TAATAAGACCTTCCT | 23092 |
| rs7723504 | snp | C/T | 0.348794 | 0.229651 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143015451 | GACAAAGCTCTAAAC[C/T]GTTTGTAGTCCTTGC | 23092 |
| rs7723598 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133618 | GTTCTGGACAAAGGT[A/G]GTCAAAAAACTTCAA | 23092 |
| rs7723834 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142900205 | CCATCTAAAAGGAAA[A/G]GTATGGGTCTTCCTC | 23092 |
| rs7724390 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142803130 | TTGAACTGAAAGTAC[A/G]TTGTGTCTTGTGTTT | 23092 |
| rs7724648 | snp | A/T | 0.0741063 | 0.177655 | intron-variant, upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:143009068 | TTGTATCAAAGAGCT[A/T]CTCTCCCCCCCTGGT | 23092 |
| rs7724961 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143170868 | GAGACTGAAGCAGCC[C/T]AGTCATGTTTCTTCT | 23092 |
| rs7725825 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143195526 | GTTGTGCAGCTTACT[C/T]AGAATGCTACATCAG | 23092 |
| rs7725832 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143003805 | TAGCTCTACTTTGCA[A/G]TGAGAAAGCAGACTC | 23092 |
| rs7725895 | snp | A/G | 0.390838 | 0.206555 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865333 | ATCTAGAAGAGGTCA[A/G]GTGCTTTCACTTAAC | 23092 |
| rs7726056 | snp | A/G | 0.407158 | 0.194426 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142865440 | AGTTATGTATAAGTC[A/G]TAGTGGGCCCAGAAC | 23092 |
| rs7727004 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142787851 | CATGATCATCCCTAT[G/T]TATCATTAACTACTC | 23092 |
| rs7727006 | snp | G/T | 0.322007 | 0.239405 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143086251 | AGGAACTAGAAAACT[G/T]CCAGTCCCCTCTGGC | 23092 |
| rs7727063 | snp | A/G | 0.298144 | 0.245321 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088709 | cttacagatggagca[A/G]cggtgagcgcacact | 23092 |
| rs7727174 | snp | C/T | 0.199254 | 0.244796 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143189150 | CAGGCCAATGTTTAC[C/T]ACTGATCTTCTTTCC | 23092 |
| rs7727753 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143133682 | CAGCTGCTTTCTTTT[C/T]CCCTGGAGAGAACAA | 23092 |
| rs7727861 | snp | A/G | 0.113334 | 0.209338 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143052088 | TGGCAGACATTTTGG[A/G]TACTGGGAAAATCAC | 23092 |
| rs7728103 | snp | C/G | 0.298398 | 0.245271 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143088687 | tacttctatagaagg[C/G]tgcgaccttacagat | 23092 |
| rs7728815 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143048996 | TCTGTCATGCAAAGT[A/G]GAAACTCTTCTTTTT | 23092 |
| rs7728894 | snp | A/G | 0.495596 | 0.0467178 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783068 | TTGGACCACACATTA[A/G]GTCTAAATAGGTCAG | 23092 |
| rs7730076 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172479 | GTTCAAAAAAAGCAT[A/G]CCAGTTCATCAAGAG | 23092 |
| rs7730315 | snp | G/T | 0.297382 | 0.245469 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143091967 | atccttttaccaaag[G/T]tttattttactttcc | 23092 |
| rs7730451 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143114228 | AGTCAGTACACAGAA[C/T]GATGTATCTGACACC | 23092 |
| rs7730716 | snp | A/G | 0.434109 | 0.169127 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143034655 | ttctggagttagata[A/G]tagtgattaatacac | 23092 |
| rs7731735 | snp | C/T | 0.0368353 | 0.130617 | intron-variant, nc-transcript-variant, upstream-variant-2KB | ARHGAP26, LOC107986457 | GRCh38.p7 | 5:142961679 | CCCTTGTGCAGTTAA[C/T]CATAGTAAGAGATAA | 23092 |
| rs7732094 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142831229 | CCAATACTCTGTGCT[C/G]AGTCATTTGATATCT | 23092 |
| rs7732115 | snp | C/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142848824 | ACCTAGCCATGGCTT[C/G]TGGGAATTAACCAGT | 23092 |
| rs7732989 | snp | G/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120103 | GAAGCTCTTGATATT[G/T]TCTCAACAAAACTGA | 23092 |
| rs7733325 | snp | C/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120337 | CCTGTGTGTTTGTTA[C/G]ACTTTGAGTGTAAGT | 23092 |
| rs7733954 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142861913 | TTTACCCACCATACC[A/T]TGTTTTTCTCTTGAT | 23092 |
| rs7734211 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143176393 | GAAAGTAAGTTTCTT[A/G]TGGGAATTTACCTGC | 23092 |
| rs7734256 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143208014 | GAAACCATCCATGCT[C/T]CCAGCCTGCTTCTGT | 23092 |
| rs7734317 | snp | C/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120198 | CAGCAAGTGAACAAT[C/T]GAGTTTTATAGCTAG | 23092 |
| rs7734323 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143120216 | GTTTTATAGCTAGGT[C/G]CTGGTGGCCTGGGTA | 23092 |
| rs7734364 | snp | C/T | 0.432504 | 0.170857 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143056587 | ATCATTCTTCAACTA[C/T]ATCATCCAGGTCCTG | 23092 |
| rs7734376 | snp | A/G | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143172759 | GTAACAGAATGATAG[A/G]TGGAAGGCAGGATCC | 23092 |
| rs7734738 | snp | G/T | 0.225597 | 0.248806 | intron-variant | ARHGAP26, ARHGAP26-AS1 | GRCh38.p7 | 5:142862448 | GTCCTCTTTTTCATT[G/T]AAAAGTTTTACAATT | 23092 |
| rs7734852 | snp | A/G | 0.318656 | 0.240388 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143020230 | TGGGATTATAGGCAT[A/G]AGCCACCACGCCCAG | 23092 |
| rs7735044 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926582 | TAATTTTAAAAGGGA[A/G]TGGTAGGCCACTTTG | 23092 |
| rs7735684 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143115114 | gaggcaggtggatca[A/C]ctgaggtcaggagtt | 23092 |
| rs7735698 | snp | C/G | 0.243919 | 0.249926 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142926990 | AACGCTGGGAGACAA[C/G]TAATTGAACTGCTCT | 23092 |
| rs7735848 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142896968 | ttTATGAGCAAACGA[A/G]TGAAGTACCAATATT | 23092 |
| rs7736251 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950180 | GGGTAGGGTGTGTGT[C/G]TCTGTGTGTGTAGTG | 23092 |
| rs7737365 | snp | C/G | | | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142950182 | GTAGGGTGTGTGTGT[C/G]TGTGTGTGTAGTGGA | 23092 |
| rs9324897 | snp | C/G | 0.491936 | 0.0629843 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142788894 | TAAGTGTTTTATAAA[C/G]TTTATTTCATTGAAC | 23092 |
| rs9324898 | snp | A/G | 0.291235 | 0.246576 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142928962 | TTTTTATTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 23092 |
| rs9324899 | snp | C/T | 0.291493 | 0.246533 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142929118 | AATTTTTGTATTTTT[C/T]AGTAGAGACAGGGTT | 23092 |
| rs9324900 | snp | A/C | 0.288906 | 0.246954 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143018772 | TAGTTATATAAGTCT[A/C]CTCTATTTATTCTCC | 23092 |
| rs9324901 | snp | A/C | 0.0810805 | 0.184299 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143083761 | acctctgcctcccaa[A/C]atgctgggattatag | 23092 |
| rs9324902 | snp | A/G | 0.136506 | 0.222754 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143102940 | GTGGTAGCCACAAAC[A/G]TTTATATAATGCCTC | 23092 |
| rs9324903 | snp | A/C | 0.310386 | 0.242597 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105251 | GCATGGTGGCACATG[A/C]TTGTAATCCTAGCTA | 23092 |
| rs9324904 | snp | C/T | 0.337614 | 0.234145 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143105261 | ACATGATTGTAATCC[C/T]AGCTACTCAGGAGGC | 23092 |
| rs9324905 | snp | C/G | 0.326741 | 0.23793 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143109275 | CAAGAGGAAAATGGG[C/G]AACAACTGCAGAAAC | 23092 |
| rs9324906 | snp | C/T | 0.106278 | 0.204558 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143111792 | TTTTTTTGGCTGTTA[C/T]ACCTTCCAGATTGTC | 23092 |
| rs9324907 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143149411 | TGCCATGGCCCTGAG[C/T]GAGAGCCATGTCAAA | 23092 |
| rs9324908 | snp | C/T | 0.105569 | 0.204058 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143210050 | ATTAGATCTAATCAG[C/T]GGTCCCATGAACTTC | 23092 |
| rs9324909 | snp | A/C | 0.494855 | 0.0504572 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143219877 | TCTGGCACATGCTTT[A/C]GTATAAATCCTGGCT | 23092 |
| rs9324910 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | ARHGAP26 | GRCh38.p7 | 5:143226181 | TTACTAACAAAATTT[C/T]GTAGCTAAAGAATGC | 23092 |
| rs9637878 | snp | A/G | 0.0123036 | 0.0774623 | upstream-variant-2KB | ARHGAP26 | GRCh38.p7 | 5:142768715 | CAGATTTACTTTCAT[A/G]GGGTTTCCATTCTAG | 23092 |
| rs9686348 | snp | A/T | 0 | 0 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142914082 | ATCTCTTCCTTTTAT[A/T]AAAAAAACATTATAC | 23092 |
| rs9686624 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142783158 | GCTCTCCAGCCTCGT[G/T]GGCACATCTCAGATA | 23092 |
| rs9686719 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:142847181 | gagtcaaatgaaaca[A/G]tgtttgtaaatttca | 23092 |
| rs9688137 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | ARHGAP26 | GRCh38.p7 | 5:143209236 | ACTCTGAGATTTGGG[G/T]CCCTGTTTCTTGTCA | 23092 |