SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9542125 | snp | A/T | 0.144969 | 0.226867 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941892 | tccctggaaatatac[A/T]atccccctagattaa | 57626 |
rs9542126 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69945168 | ttttttgtatgttta[A/G]aacagacggggtttc | 57626 |
rs9542127 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69945400 | gcaagactgagctaa[A/G]atcatgccactgcac | 57626 |
rs9542128 | snp | C/T | 0.481087 | 0.0953875 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945619 | actgggcaaatgatt[C/T]atacagacatcccac | 57626 |
rs9542129 | snp | C/T | 0.422315 | 0.181128 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950343 | GAAGAGAACAAGGAA[C/T]TGTTTTCAGAGTAAA | 57626 |
rs9542130 | snp | C/T | 0.423881 | 0.179625 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950597 | TGATTAACTCATGGT[C/T]GTAGAAGTTATTTAA | 57626 |
rs9542131 | snp | A/G | 0.455977 | 0.141681 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953230 | TGCTAAGAAGCATCA[A/G]TGACAATTCTCCATT | 57626 |
rs9542132 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962254 | CTTTTTATTCTATTT[C/T]TGTTGGTTTGTTTTT | 57626 |
rs9542133 | snp | A/T | 0.454182 | 0.144256 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964480 | GTGGGACTTAATATT[A/T]ACTCAGCATATGTTT | 57626 |
rs9542134 | snp | C/T | 0.479421 | 0.0993283 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964503 | ATATGTTTTTCTGAG[C/T]TTCCTGGAGCAGTGC | 57626 |
rs9542135 | snp | C/T | 0.451856 | 0.147493 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964771 | TTTATTCATTGTTAT[C/T]TATCTTCTCCTATAA | 57626 |
rs9542136 | snp | C/T | 0.479421 | 0.0993283 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964916 | TTCTCCTGCATTTTC[C/T]GTCTACAGTAAAATT | 57626 |
rs9542137 | snp | G/T | 0.480064 | 0.0978296 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967025 | attgatgaacaatta[G/T]gttgattccatatat | 57626 |
rs9542138 | snp | C/T | 0.480302 | 0.0972668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967041 | gttgattccatatat[C/T]tgatattgtgaatag | 57626 |
rs9542139 | snp | C/T | 0.422315 | 0.181128 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971770 | GTTTATCTTTAATTC[C/T]TCAAGTATATTGAAA | 57626 |
rs9542140 | snp | C/G | 0.42803 | 0.175514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972498 | CATATTGCATGCTTG[C/G]TGTAAAAATTTAAAT | 57626 |
rs9542141 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972903 | CTCATCTGAATCTCA[C/G]ATTAAAGGTAGCCTA | 57626 |
rs9542142 | snp | A/G | 0.477515 | 0.103619 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974994 | TCCCCATGTATTCCA[A/G]GACACTGACTTAAAT | 57626 |
rs9542143 | snp | A/T | 0.473174 | 0.112665 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975896 | CAGGTTTTTATCATT[A/T]TCTTAAGAAAACTAA | 57626 |
rs9542144 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978717 | GTCTTGAACTCCCGA[A/C]CTCAGGTGATCTGCC | 57626 |
rs9542145 | snp | G/T | 0.19334 | 0.243495 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983532 | gatttcttgaagcca[G/T]gagtttgagaccatc | 57626 |
rs9542147 | snp | G/T | 0.183568 | 0.241012 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988936 | ttgttctgttgatag[G/T]ttcttttgctgtgca | 57626 |
rs9542148 | snp | A/G | 0.499693 | 0.0123764 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989936 | atttcctctcttcct[A/G]tttggatgcctttta | 57626 |
rs9542149 | snp | C/T | 0.27893 | 0.24832 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999303 | ATGATTACCGGAAGG[C/T]GAAGATCATCGGTGG | 57626 |
rs9542150 | snp | C/T | 0.281577 | 0.247998 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999540 | GGGCTCCCCAAGCCA[C/T]TGAATCGATAGGTAA | 57626 |
rs9542151 | snp | A/G | 0.281841 | 0.247964 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999888 | CACTTTCCTTTTATG[A/G]ATACTAATATAGTCG | 57626 |
rs9542152 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000309 | TTATCAAAGAGTCTG[C/T]CAGGAAGAAATTGTG | 57626 |
rs9542153 | snp | C/T | 0.279195 | 0.248289 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001564 | TAAACATTGGGATAT[C/T]TATCTATGATCTATG | 57626 |
rs9542154 | snp | A/C | 0.279195 | 0.248289 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001778 | ACTATGTCAGTAGAC[A/C]ATGAAATCAAAAATT | 57626 |
rs9542155 | snp | C/T | 0.467946 | 0.122472 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005395 | AGCCTGCAAGCCACA[C/T]GCAGCCCAAGATAGC | 57626 |
rs9542157 | snp | C/T | 0.490727 | 0.0674567 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010752 | aaaaaattagctggg[C/T]gtggtggtgggtgct | 57626 |
rs9542158 | snp | C/G | 0.413914 | 0.188765 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011900 | TTAATGGACTTAAGA[C/G]TTTCACGTGGCTGGG | 57626 |
rs9542159 | snp | A/G | 0.41325 | 0.18934 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013313 | GAATGCAGAGAACCC[A/G]TCAGCAAATACCAAT | 57626 |
rs9542160 | snp | A/C | 0.413083 | 0.189483 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015195 | TCCACTTGTGAACAT[A/C]ATAGAGTGGACTTAT | 57626 |
rs9542161 | snp | A/G | 0.41325 | 0.18934 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015531 | GTGCAAAAGCAATGC[A/G]TATTTAGCATAAACC | 57626 |
rs9542162 | snp | A/C | 0.357238 | 0.225832 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020664 | AGATAACCCAGGTAC[A/C]TAAAGGCAGTCATCA | 57626 |
rs9542163 | snp | A/G | 0.361474 | 0.223771 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020743 | AGTGACAATACTAGT[A/G]TATCAATAGAATATT | 57626 |
rs9542164 | snp | A/G | 0.413914 | 0.188765 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022506 | AAATGAAAAAATTAT[A/G]TATACTTAATACAAT | 57626 |
rs9542165 | snp | C/T | 0.465683 | 0.126415 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030650 | aaagcaggaaagatc[C/T]aaaattgacacccta | 57626 |
rs9542166 | snp | C/T | 0.189576 | 0.242588 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039484 | ccaatatatgattgg[C/T]aaagattttctccaa | 57626 |
rs9542167 | snp | C/T | 0.322007 | 0.239405 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058945 | tatcaaaggtgccga[C/T]aatatacaatgggga | 57626 |
rs9542168 | snp | C/T | 0.440057 | 0.162414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059071 | aaaataaaaatggat[C/T]aaatactaaaacctc | 57626 |
rs9542169 | snp | C/T | 0.395453 | 0.203331 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060962 | gggacactatgttaa[C/T]agaaatatgccaggc | 57626 |
rs9542170 | snp | C/T | 0.315758 | 0.241197 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066877 | CATTTTATATAACAG[C/T]TCTAAAATAATAATC | 57626 |
rs9542171 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066986 | TTTTAAGTATAAAAT[A/C]AAATTTATCAAGCAC | 57626 |
rs9542172 | snp | C/T | 0.204803 | 0.245881 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070116 | gaggttgcagggagc[C/T]gagtccagcctgggt | 57626 |
rs9542173 | snp | C/T | 0.177503 | 0.239258 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072760 | tatttatgataaaag[C/T]gctcagctggtgcta | 57626 |
rs9542174 | snp | G/T | 0.491629 | 0.0641526 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089062 | GACTAACTATGGCAT[G/T]CTAGCCTAGAGACAC | 57626 |
rs9542175 | snp | A/G | 0.361263 | 0.223876 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093374 | GGGCATCTCTGAAGT[A/G]CTTTTAGGTAACCAA | 57626 |
rs9542176 | snp | C/T | 0.268724 | 0.249298 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099558 | AACAAACTCAAGAAG[C/T]ATTTGGCCCCAACAT | 57626 |
rs9542177 | snp | A/G | 0.345925 | 0.230864 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105872 | ATGGAAAAACCATTG[A/G]CACAATTGATAATTC | 57626 |
rs9542178 | snp | A/G | 0.34989 | 0.229177 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110114 | AGGACAATATTTTAT[A/G]TGACCCAAAGGAGAT | 57626 |
rs9564592 | snp | A/C | 0.497722 | 0.0336691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714477 | TTGGATACGCTTAAC[A/C]GTTCAAAACTAAAGA | 57626 |
rs9564593 | snp | A/G | 0.463559 | 0.129972 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722250 | TATTGAGTTATTTGA[A/G]CCAAATATTGTTGAT | 57626 |
rs9564595 | snp | A/G | 0.404907 | 0.196224 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741790 | tcacaacccaggact[A/G]tctttctcaaggact | 57626 |
rs9564596 | snp | A/C | 0.434976 | 0.168179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742130 | tacaattgcctcata[A/C]aattttgctttGAGA | 57626 |
rs9564597 | snp | A/G | 0.360632 | 0.224189 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742940 | GCTTTTTAGAGAAGT[A/G]TAGGTAGATATTCAC | 57626 |
rs9564599 | snp | A/G | 0.356597 | 0.226135 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744309 | ATGGGCTTATCATTG[A/G]CTTTCATATTTCTGA | 57626 |
rs9564600 | snp | C/T | 0.474903 | 0.109173 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747304 | ATGTAATATAATCTA[C/T]TGTATTGATTGTCAT | 57626 |
rs9564601 | snp | A/C | 0.371987 | 0.218218 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747580 | CTCAAGCCTCAGGGA[A/C]AATATAAAAAGGAAA | 57626 |
rs9564602 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751108 | TCATTCATGTCAtgt[G/T]tgtatgtgtgtgtgt | 57626 |
rs9564603 | snp | C/T | 0.324619 | 0.238604 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755413 | AACATCTTCTCTTTA[C/T]AGATTACCCAGTCTC | 57626 |
rs9564604 | snp | A/G | 0.381503 | 0.21262 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759846 | CATAGGCAAAGGCCC[A/G]GTTAAGACAAGATTG | 57626 |
rs9564605 | snp | A/G | 0.383824 | 0.211166 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761201 | tttcagagtgactcc[A/G]gggctgccacatggt | 57626 |
rs9564606 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772962 | ATTAAGAGGAATATT[A/C]TTGGATTCTTGAAAA | 57626 |
rs9564607 | snp | C/T | 0.347914 | 0.230028 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773039 | TTGTAGACCATTACA[C/T]AGGCAGAAAACAGAA | 57626 |
rs9564608 | snp | C/T | 0.384017 | 0.211044 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776762 | GCAATAAATTAGCAT[C/T]CAAAATCAGAATAAC | 57626 |
rs9564609 | snp | C/T | 0.383824 | 0.211166 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777767 | CAGAGCACCCTTACT[C/T]ATTGTATGTATAACT | 57626 |
rs9564610 | snp | A/T | 0.456214 | 0.141336 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777865 | AATACCTTACTTATC[A/T]TTTTATTCTGAGTAT | 57626 |
rs9564611 | snp | G/T | 0.482683 | 0.0914256 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782837 | ccagcacgcagctgg[G/T]gatctgagaatgagc | 57626 |
rs9564612 | snp | A/C | 0.497359 | 0.0362457 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783160 | gaaaggacatccaca[A/C]caaaaacccttctgt | 57626 |
rs9564613 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69784349 | atgttaactttaaat[A/G]taaatggactaaatg | 57626 |
rs9564614 | snp | C/T | 0.451732 | 0.147663 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789195 | AGGAATCTTTAGGAT[C/T]GATCTATGCTATCAA | 57626 |
rs9564615 | snp | A/C | 0.460925 | 0.134204 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789460 | AAGTTTTCCTTGTAA[A/C]GTGATGTGAAATAGG | 57626 |
rs9564616 | snp | A/G | 0.395453 | 0.203331 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789461 | AGTTTTCCTTGTAAC[A/G]TGATGTGAAATAGGG | 57626 |
rs9564618 | snp | A/G | 0.459347 | 0.136653 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803466 | CAATTAATATATGCA[A/G]TGGGTAGAATTTAAA | 57626 |
rs9564619 | snp | C/T | 0.396182 | 0.202807 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803528 | TTTCCAGAACCTGTG[C/T]ATATGTTGAAATATC | 57626 |
rs9564620 | snp | A/G | 0.461481 | 0.133325 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808603 | ttaaaaaagaaatac[A/G]aagtgtcagctctca | 57626 |
rs9564623 | snp | C/T | 0.466515 | 0.124985 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821181 | ATACAAAACAAATGG[C/T]AGGCTAGATATGGTC | 57626 |
rs9564627 | snp | G/T | 0.387074 | 0.209071 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878711 | GCATATATATATATA[G/T]AGAGAGAGAGAGAGA | 57626 |
rs9564628 | snp | A/G | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885176 | CGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC | 57626 |
rs9564629 | snp | A/C | 0.120674 | 0.21395 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886333 | TTTTTCTAGCTAAAA[A/C]AATGTAGTTTTGTTT | 57626 |
rs9564630 | snp | A/G | 0.143959 | 0.226396 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904746 | CAGTCTGGCTCCAGA[A/G]TTTACGCTTAATCAT | 57626 |
rs9564632 | snp | A/C | 0.450483 | 0.149354 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932724 | AGCTATGTGTTATAT[A/C]TTAATGTTTTAGAAA | 57626 |
rs9564633 | snp | A/G | 0.45889 | 0.13735 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933095 | CATTGTCCCTTAAAC[A/G]TTCATTATACTCACC | 57626 |
rs9564634 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69935192 | cacctactggtgaac[G/T]tggtacatagttggt | 57626 |
rs9564635 | snp | G/T | 0.479421 | 0.0993283 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968100 | tcctattttaagaat[G/T]gccacagatactcca | 57626 |
rs9564636 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985794 | tatatatatatatat[A/T]ttatatatatttata | 57626 |
rs9564637 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985797 | atatatatatatttt[A/T]tatatatttatatat | 57626 |
rs9564638 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985814 | atatatttatatatt[A/T]tatattatatatata | 57626 |
rs9564639 | snp | A/G | 0.49975 | 0.0111793 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000059 | GGTCTGTTAGTTCCC[A/G]TGAGATCTGATTGTT | 57626 |
rs9564640 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022305 | tgtgtgtgtgtgtgt[A/G]tgtgtTTGGTTGTAG | 57626 |
rs9564641 | snp | G/T | 0.44858 | 0.151875 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029939 | aacaaaaaaaggcag[G/T]ggttgcaatcctagt | 57626 |
rs9564642 | snp | G/T | 0.46137 | 0.133501 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060353 | ctatagagaacagta[G/T]gcaggttctgcaaaa | 57626 |
rs9564643 | snp | A/G | 0.451856 | 0.147493 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062120 | TTACCTTTCCCATCC[A/G]CTAGGTATCTGATTC | 57626 |
rs9564644 | snp | A/G | 0.305934 | 0.243663 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069706 | tttaataggctcatc[A/G]gaagactgaacaaaa | 57626 |
rs9564645 | snp | C/G | 0.499451 | 0.0165644 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071109 | tccaacaattaaaag[C/G]cTAAGCAACGGGGAA | 57626 |
rs9564646 | snp | C/T | 0.317933 | 0.240593 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072134 | tcactattgatccca[C/T]agacattaactgtat | 57626 |
rs9564647 | snp | A/G | 0.316243 | 0.241064 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074079 | tgatccgcccacctc[A/G]gcctcccaaagtgct | 57626 |
rs9564648 | snp | A/G | 0.384017 | 0.211044 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092152 | GATTTCAGCCTATGC[A/G]ATTGAGCAGAGGACA | 57626 |
rs9564649 | snp | A/G | 0.3529 | 0.227852 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107173 | TGGAAATTGAGAGAT[A/G]CTTGGAAGCCCCGTG | 57626 |
rs9572240 | snp | G/T | 0 | 0 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700322 | TAATAAAAGAAGGTT[G/T]TCTTGCCTCTTCTAG | 57626 |
rs9572241 | snp | C/T | 0.305934 | 0.243663 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710260 | CATATTTAAAAAATA[C/T]TAACCTGCAATCAGA | 57626 |
rs9572242 | snp | A/G | 0.412249 | 0.190198 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714126 | AGGAAGATGGAAAAA[A/G]TAAATTTCTGCTTCC | 57626 |
rs9572243 | snp | A/T | 0.496175 | 0.0435625 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714865 | TCCAAAGGTGCCAGT[A/T]TTACAGGTGTGAGCC | 57626 |
rs9572244 | snp | C/T | 0.496175 | 0.0435625 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714866 | CCAAAGGTGCCAGTA[C/T]TACAGGTGTGAGCCA | 57626 |
rs9572245 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721646 | TTACAAATTCATGCT[C/T]TAATACCATATAATA | 57626 |
rs9572247 | snp | A/T | 0.342806 | 0.232136 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724363 | accttggcaatataa[A/T]ctttctaaattgact | 57626 |
rs9572248 | snp | G/T | 0.184203 | 0.241186 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724454 | attcttctcaaattc[G/T]ttcatatattgaaga | 57626 |
rs9572249 | snp | C/T | 0.33875 | 0.233717 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724463 | aaattcgttcatata[C/T]tgaagacagaacact | 57626 |
rs9572250 | snp | A/G | 0.372391 | 0.217992 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728046 | TCAATCAGGTCCCTT[A/G]AAAATCATCTCTTTC | 57626 |
rs9572251 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728606 | tcaggagttggagac[C/G]aacctggccaacatg | 57626 |
rs9572252 | snp | C/T | 0.36955 | 0.219562 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729803 | TGGAGCCATTCAAAA[C/T]ATTTTCACAGAATAG | 57626 |
rs9572253 | snp | C/T | 0.327445 | 0.237702 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733423 | ATTACATAATCAACA[C/T]GTACTTACTGGAAAG | 57626 |
rs9572254 | snp | C/T | 0.375399 | 0.216275 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733965 | aactacactcagtag[C/T]tgagtgtaggagaat | 57626 |
rs9572256 | snp | A/T | 0.360842 | 0.224085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741842 | aatttagtcattaag[A/T]tattctatctcccag | 57626 |
rs9572257 | snp | A/G | 0.371785 | 0.218331 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748054 | ATCTCTCTACTGGAG[A/G]TACAATAGAGCCTAT | 57626 |
rs9572258 | snp | A/G | 0.475348 | 0.108251 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748110 | AACATATAAATATTG[A/G]AAGATTTATATATTA | 57626 |
rs9572259 | snp | C/T | 0.475437 | 0.108066 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748119 | ATATTGAAAGATTTA[C/T]ATATTACTATCTTTT | 57626 |
rs9572260 | snp | A/G | 0.456214 | 0.141336 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757506 | atatgtcagatatga[A/G]tgtttattatttcta | 57626 |
rs9572261 | snp | A/G | 0.368529 | 0.220116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757690 | ctggcagtggcttac[A/G]cctgtaatcccagca | 57626 |
rs9572262 | snp | A/G | 0.381891 | 0.212379 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760011 | CAAAAAGACACCCTC[A/G]CGAATGGAGGTTTTC | 57626 |
rs9572263 | snp | C/T | 0.456332 | 0.141164 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760418 | tggagtgcaagagca[C/T]gatctcagctcactg | 57626 |
rs9572264 | snp | A/C | 0.368733 | 0.220005 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760740 | ggaggcaatacaaat[A/C]ctgaaatatttttag | 57626 |
rs9572265 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766317 | TTATACATTAGCTGT[C/T]TCAAATATGCAAATG | 57626 |
rs9572266 | snp | G/T | 0.455858 | 0.141853 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767476 | CTGAGGTGGGAGAAT[G/T]GCTTGAGGCCAGGAG | 57626 |
rs9572267 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768713 | GTAATTATTAATAAC[G/T]TCATTAGTTAATACA | 57626 |
rs9572268 | snp | A/C | 0.38286 | 0.211774 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769393 | TAGCATAAAAGGCAA[A/C]GGAAAAATACTGAtg | 57626 |
rs9572269 | snp | G/T | 0.420892 | 0.182472 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770127 | tataacacccccttg[G/T]gactccatgatggct | 57626 |
rs9572270 | snp | C/T | 0.384017 | 0.211044 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772777 | TTTCTGAATAAAGTG[C/T]CTTAAAAAGAGCCTG | 57626 |
rs9572271 | snp | A/T | 0.45645 | 0.140991 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772999 | ATAATTTCAGGAAGA[A/T]CCGAGTGAGAAAGCA | 57626 |
rs9572272 | snp | G/T | 0.479421 | 0.0993283 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773897 | TACATAGAATAAAAC[G/T]TATTGTGGGAGTTTC | 57626 |
rs9572273 | snp | G/T | 0.384017 | 0.211044 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775702 | CTAAGGGTTTTTTTT[G/T]GTTTTTGATACAGTG | 57626 |
rs9572274 | snp | A/G | 0.347914 | 0.230028 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776151 | ACAGAGTGAGACTCC[A/G]TCTCGGAAAAAAAAA | 57626 |
rs9572275 | snp | A/G | 0.347694 | 0.230122 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776156 | GTGAGACTCCGTCTC[A/G]GAAAAAAAAATAAAA | 57626 |
rs9572276 | snp | A/C | 0.399253 | 0.200558 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781932 | TTTTATTGCTTTTAA[A/C]GAGATGACATCAATT | 57626 |
rs9572277 | snp | A/G | 0.399253 | 0.200558 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781933 | TTTATTGCTTTTAAA[A/G]AGATGACATCAATTG | 57626 |
rs9572278 | snp | A/G | 0.394171 | 0.204242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782239 | cccagcgtgagcgac[A/G]cagaagatgggtgct | 57626 |
rs9572279 | snp | C/T | 0.455858 | 0.141853 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782247 | gagcgacgcagaaga[C/T]gggtgctttctgcat | 57626 |
rs9572280 | snp | A/C | 0.455858 | 0.141853 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782253 | cgcagaagatgggtg[A/C]tttctgcatttccat | 57626 |
rs9572281 | snp | A/G | 0.401392 | 0.198948 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782807 | ctgacagctttgaag[A/G]gagtagtggttctcc | 57626 |
rs9572282 | snp | C/T | 0.449726 | 0.150364 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783090 | tggacctctagcaaa[C/T]tccaacagacctgca | 57626 |
rs9572283 | snp | A/G | 0.461037 | 0.134028 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788340 | gcagccataaaaaat[A/G]aagagttcacgtcct | 57626 |
rs9572284 | snp | A/G | 0.460925 | 0.134204 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789309 | ATGGGTAACTTGACA[A/G]AATAAGTCTTATTTA | 57626 |
rs9572285 | snp | A/G | 0.460925 | 0.134204 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789393 | TTTTGGCAACAGCAT[A/G]TATGTTAGAAAAAAT | 57626 |
rs9572286 | snp | C/T | 0.385932 | 0.209815 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790142 | GATCACTTAGTTTAT[C/T]CTTGTTGTACCCATA | 57626 |
rs9572287 | snp | A/C | 0.450859 | 0.148847 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790521 | CAGTATCTCTTGTGA[A/C]TATAGATGTGAAATC | 57626 |
rs9572288 | snp | A/G | 0.451133 | 0.149383 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790565 | TAACAAACAAATAAA[A/G]AAATACAGCAAAATA | 57626 |
rs9572289 | snp | A/G | 0.386313 | 0.209568 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790609 | ACACTGTGACTAAGT[A/G]TAATGTATTTGAAAA | 57626 |
rs9572290 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794557 | cagagaaagaggaga[A/G]agagattaaaaaaaa | 57626 |
rs9572291 | snp | C/T | 0.455024 | 0.143057 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800697 | CTCATTCTATAATTA[C/T]TATTAATTTATCAAT | 57626 |
rs9572292 | snp | A/C | 0.47666 | 0.105476 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802547 | gcgccacaccctggg[A/C]ctggtagttaaagat | 57626 |
rs9572293 | snp | C/G | 0.476401 | 0.106032 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802773 | gacaggaattgctca[C/G]tcagggagctcggct | 57626 |
rs9572294 | snp | A/G | 0.465158 | 0.127307 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803800 | CTCTAGAAGCTGAGA[A/G]TGATTCTGACCTGAC | 57626 |
rs9572295 | snp | C/T | 0.456095 | 0.141508 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806392 | GATGGCTGACTAGAC[C/T]CAAGTAGCATGTACC | 57626 |
rs9572297 | snp | A/G | 0.181659 | 0.240478 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814580 | aagtgggcaaaggac[A/G]tgaacagatacatct | 57626 |
rs9572299 | snp | C/G | 0.397452 | 0.201886 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841176 | TTTCCCCTTCAATAT[C/G]ACATCTCAtattcaa | 57626 |
rs9572300 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69842224 | aaaaagcttctgcac[A/G]acaaaggaaaaaaat | 57626 |
rs9572301 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881566 | CTGAATTAACAATGC[C/T]GTACATAGAGAATTT | 57626 |
rs9572302 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884939 | TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTGAG | 57626 |
rs9572303 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885295 | TCCAATAATTTTGTA[C/T]TTTTATAAGTTACAC | 57626 |
rs9572304 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886797 | TAAGACTTATGTCTT[A/T]CCATCTTATACTCTG | 57626 |
rs9572305 | snp | A/C | 0.198324 | 0.244601 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894129 | AAAGAACATTTATTT[A/C]GATTTTTTTGAAGTC | 57626 |
rs9572306 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903978 | TTTATGTTCATTGAA[A/G]AAATGTTTACTATAT | 57626 |
rs9572307 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904012 | CTATGTATTTAAAGA[A/G]ACCCACTTGAAATGA | 57626 |
rs9572309 | snp | A/G | 0.36021 | 0.224397 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919121 | TTTTGCCTGAGGAGC[A/G]GCAACAATCTTGAGA | 57626 |
rs9572310 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929112 | AAATTTAAGATTTAA[C/T]AAGATATTTGTAGAA | 57626 |
rs9572311 | snp | A/C | 0.452719 | 0.146304 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929600 | TTGGTGGTGCTGTAT[A/C]ATCTCATATATTATT | 57626 |
rs9572312 | snp | C/T | 0.441705 | 0.160466 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934031 | TTCTAGCATGTCTAT[C/T]TATTGATCCTGAGTA | 57626 |
rs9572313 | snp | A/C | 0.454423 | 0.143914 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957280 | ATTTTACTACTTTTA[A/C]AAACAAAAGTAAAGG | 57626 |
rs9572314 | snp | C/T | 0.479258 | 0.0997024 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962641 | AAACAATTTTTATAT[C/T]TGTGTATTAAAATTT | 57626 |
rs9572315 | snp | A/G | 0.479258 | 0.0997024 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963068 | TTGTTTATAATTTCA[A/G]CATTTTTTTTAGAGA | 57626 |
rs9572316 | snp | A/G | 0.484701 | 0.0861117 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963341 | GATTAATCTTTGTAC[A/G]GTAATTATTTCATAT | 57626 |
rs9572317 | snp | G/T | 0.479095 | 0.100076 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963602 | AGCTGCACAGCAGAT[G/T]TGGCCCCTGCACAGA | 57626 |
rs9572318 | snp | A/G | 0.479984 | 0.0980171 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964100 | CCAGGCTGGAGTCCA[A/G]TGGCACAATCATAGC | 57626 |
rs9572319 | snp | C/T | 0.479095 | 0.100076 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967809 | agaattgcttgaacc[C/T]gggaagcggagattg | 57626 |
rs9572321 | snp | C/T | 0.479421 | 0.0993283 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968112 | aatggccacagatac[C/T]ccagccttctgcaac | 57626 |
rs9572322 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968161 | gaagccatcaacagc[A/G]agttaagacccatca | 57626 |
rs9572323 | snp | C/G | 0.482083 | 0.0929373 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974431 | ACTAATGTATATAAA[C/G]AGTAATAAAGAAAAC | 57626 |
rs9572324 | snp | C/T | 0.373196 | 0.217538 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976177 | TGATATTGAGGAAGA[C/T]AGCTTAATTATACTA | 57626 |
rs9572325 | snp | G/T | 0.43088 | 0.172575 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979003 | CATAGTATTTGAAAA[G/T]AGTTATTCAAAGTCA | 57626 |
rs9572326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982868 | gaaatcctagccaga[G/T]cattaggcaagagaa | 57626 |
rs9572327 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985805 | atattttatatatat[A/T]tatatattatatatt | 57626 |
rs9572328 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985807 | attttatatatattt[A/T]tatattatatattat | 57626 |
rs9572329 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985813 | tatatatttatatat[A/T]atatattatatatat | 57626 |
rs9572330 | snp | A/C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985820 | ttatatattatatat[A/C/T]atatatatatcttat | 57626 |
rs9572331 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985821 | tatatattatatatt[A/T]tatatatatcttatg | 57626 |
rs9572332 | snp | A/G | 0.312104 | 0.242163 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997181 | agccaatatcacgcc[A/G]ctgcactccagcctg | 57626 |
rs9572333 | snp | C/G | 0.313082 | 0.241911 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009547 | CTTATATTCTACTAC[C/G]TTCCAGCGATGCGAC | 57626 |
rs9572334 | snp | C/G | 0.412082 | 0.190341 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010868 | ttgcactccagcctg[C/G]gcaacaaaagtgaaa | 57626 |
rs9572335 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011890 | AGAAAGATGTTTAAT[A/G]GACTTAAGAGTTTCA | 57626 |
rs9572336 | snp | C/T | 0.256061 | 0.249927 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024971 | GCTCCTAATATGTGC[C/T]AGACACTTTAGATAT | 57626 |
rs9572337 | snp | A/C | 0.268452 | 0.249318 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024997 | GATATTTTTTATAAG[A/C]CTCACAATAGTCTCA | 57626 |
rs9572338 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027878 | CACAGTTAATTTTTA[A/G]AGGCTGGAGTTATTG | 57626 |
rs9572339 | snp | A/G | 0.431621 | 0.171796 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029308 | ACTTTCTATGGCATT[A/G]AAAAGGCTGGTCACT | 57626 |
rs9572340 | snp | C/T | 0.428333 | 0.175206 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030917 | taaaggggatatcac[C/T]accaatcccacagaa | 57626 |
rs9572341 | snp | A/T | 0.428484 | 0.175052 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031032 | acatacaccctccca[A/T]gactaaaccaggaag | 57626 |
rs9572342 | snp | C/T | 0.352287 | 0.228117 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034143 | ACTTTCCGGAACTTA[C/T]GTACCATGAATTCAT | 57626 |
rs9572343 | snp | A/T | 0.397994 | 0.201489 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036791 | TTGTTTCCTTTTACG[A/T]TTTTCTTTCTAGCCC | 57626 |
rs9572345 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048577 | tttccacagatggca[A/G]gctagggtagagaag | 57626 |
rs9572346 | snp | C/T | 0.236144 | 0.249616 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057965 | tgtacaaatcaatca[C/T]atcaacagaataaag | 57626 |
rs9572347 | snp | C/T | 0.474903 | 0.109173 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061182 | ATTTTCTGTTAGTAA[C/T]CATCACAGTTTACAG | 57626 |
rs9572348 | snp | A/C | 0.302936 | 0.244331 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069580 | attaaatggtaatag[A/C]agacaacatgcaata | 57626 |
rs9572349 | snp | A/G | 0.318896 | 0.240319 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070335 | aatcaaggagaaaga[A/G]gacatattggaagaa | 57626 |
rs9572350 | snp | A/G | 0.491368 | 0.0651254 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072954 | aagttctagctaatg[A/G]aataagagaagaaaa | 57626 |
rs9572351 | snp | A/G | 0.304438 | 0.244001 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076201 | taagaaaaaggtaaa[A/G]tcggaggattgacac | 57626 |
rs9572352 | snp | A/C | 0.304188 | 0.244057 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079770 | AATGAGGAAACGAAG[A/C]ATTAGTGATGTTAAT | 57626 |
rs9572353 | snp | C/T | 0.313814 | 0.241719 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081737 | aacaaatacctggat[C/T]gtggcctagtgaaac | 57626 |
rs9572354 | snp | A/G | 0.31503 | 0.241394 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081984 | ttggatcatggggac[A/G]cacttctcacttgct | 57626 |
rs9572355 | snp | C/T | 0.370974 | 0.218781 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084977 | GTTCAATTCAGTTAA[C/T]GGATGAATTGAGTTT | 57626 |
rs9572356 | snp | A/G | 0.237303 | 0.249677 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085026 | CCATCCATTGATGAC[A/G]TGAATATGGTAAATG | 57626 |
rs9572357 | snp | C/T | 0.368324 | 0.220226 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085118 | GAGTGTGTATGGATA[C/T]ATGTATGTGCATGTA | 57626 |
rs9572358 | snp | C/T | 0.371582 | 0.218444 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085506 | TTTAAATGTTTAATT[C/T]TTTTATATTTACATT | 57626 |
rs9572359 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085864 | caagactctgtctca[A/G]aaaccacaaacaaaa | 57626 |
rs9572360 | snp | A/G | 0.3746 | 0.216737 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086309 | TAGACCTGGCTGGGC[A/G]TGGAGGCTCATGCCT | 57626 |
rs9572361 | snp | C/T | 0.315273 | 0.241329 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089798 | TATAGAAGTGAACTG[C/T]AGAAAAGAAGTGTGA | 57626 |
rs9572362 | snp | A/T | 0.31503 | 0.241394 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090031 | CCATTTAATCAATAG[A/T]ATTGATAATAGAATT | 57626 |
rs9572363 | snp | A/G | 0.281841 | 0.247964 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090076 | CCTAACTCTGTTTTT[A/G]TATGGGAAATGAATT | 57626 |
rs9572364 | snp | C/T | 0.288906 | 0.246954 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091881 | CTGAAATTTTTCACA[C/T]GGATGTGTAGATAAA | 57626 |
rs9572365 | snp | C/T | 0.288646 | 0.246995 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093081 | TTATTTCAGCATTTA[C/T]AATTATTTAACCTTA | 57626 |
rs9572366 | snp | C/T | 0.288906 | 0.246954 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093652 | TAATTTGGCAAATAA[C/T]TTTTTTCTCTAAATT | 57626 |
rs9572367 | snp | A/G | 0.47885 | 0.100637 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094369 | AAATAAAATTCACAT[A/G]AAACAAATACAATGC | 57626 |
rs9572368 | snp | A/G | 0.305934 | 0.243663 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095222 | GAGACCCTCTATAAA[A/G]GAGGCTTTTGCACCA | 57626 |
rs9572369 | snp | C/T | 0.401747 | 0.198678 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095975 | tctggcttatttcac[C/T]taacataaggccatc | 57626 |
rs9572370 | snp | C/T | 0.268452 | 0.249318 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100789 | TGACCTAAATCAATA[C/T]GAAAACTTCAGACCA | 57626 |
rs9572371 | snp | C/T | 0.0232847 | 0.105357 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105906 | ATTATACTTCTCCCT[C/T]ATTAAAATTATCTTA | 57626 |
rs9592651 | snp | A/G | 0.448452 | 0.152042 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711555 | AGGTTTCATGACATT[A/G]TCAAAAGAAATGTTC | 57626 |
rs9592652 | snp | A/G | 0.130008 | 0.219321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741118 | TTATGTAAAGCTTAG[A/G]AAATATGACATCTTT | 57626 |
rs9592653 | snp | C/G | 0.1652 | 0.235179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749704 | TGAAGAAGATAATCT[C/G]TCTATACAGATCATT | 57626 |
rs9592654 | snp | G/T | 0.3746 | 0.216737 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754072 | GTCTCGAACTCCTGG[G/T]CTCAAGCAATCCACC | 57626 |
rs9592655 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760074 | atagtctggtaaatg[A/T]caaaaacgtaaattt | 57626 |
rs9592659 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69815668 | agcatcacgcaatat[A/T]cccatgcaacaaaca | 57626 |
rs9592660 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824935 | aaaaaAATTTGAAAT[C/G]TAATGATAATATGTA | 57626 |
rs9592661 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829929 | actgccaagccagca[C/G]tacaagaactgctaa | 57626 |
rs9592662 | snp | A/C | 0.0923359 | 0.194016 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850076 | TTCGATAGCAAAAAT[A/C]CATTACAGAAATAAT | 57626 |
rs9592666 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69902049 | aggtgatctgcccac[C/T]tcagcctcccagagt | 57626 |
rs9592667 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937715 | CCAAGCTGAGTCACC[C/T]TCCCAAAAGATTTCG | 57626 |
rs9592668 | snp | A/T | 0.270892 | 0.249126 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961223 | ATACAGAATTTTTTT[A/T]AAAAAAGCGTTAAAT | 57626 |
rs9592669 | snp | G/T | 0.36606 | 0.221428 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973838 | TATAGTGTTAAAAAT[G/T]TAATTGGGAGGTCAT | 57626 |
rs9592670 | snp | C/T | 0.483418 | 0.0895317 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977696 | CCTAATACACTGATT[C/T]GGAAAACATTATATT | 57626 |
rs9592671 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69997666 | tgactaaataatata[A/T]tatatataatattac | 57626 |
rs9592672 | snp | G/T | 0.279195 | 0.248289 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004174 | TATCTAATGATTGGT[G/T]AATATAAATGGAAGG | 57626 |
rs9592673 | snp | C/G | 0.405082 | 0.196086 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010246 | gttttagaagtatca[C/G]tagtgttatgtatag | 57626 |
rs9592675 | snp | C/T | 0.398534 | 0.201091 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063376 | TAAAAACTGCAATTA[C/T]AGCTTTTACAGATTT | 57626 |
rs9599498 | snp | C/G | 0.448323 | 0.15221 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711390 | CTGCTTCAAAAGAAT[C/G]GCACATAGATTTCAA | 57626 |
rs9599499 | snp | A/T | 0.448323 | 0.15221 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711936 | GGTGATGGTATAATA[A/T]TGTAATTTTAATTTG | 57626 |
rs9599500 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719209 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 57626 |
rs9599501 | snp | C/T | 0.130008 | 0.219321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740098 | GTAAAGAAAGATATA[C/T]TGAACACCAAACTTT | 57626 |
rs9599502 | snp | A/T | 0.0865458 | 0.189163 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743916 | AGAAAAGTTTGAAAA[A/T]TATTTTTggggaaag | 57626 |
rs9599504 | snp | A/G | 0.372592 | 0.217879 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745427 | ATATTTGCATTACAG[A/G]TCTTTTTCCACTGTG | 57626 |
rs9599505 | snp | G/T | 0.475965 | 0.106957 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745765 | CATGAAAAATACTTG[G/T]TCTAAATTTTAAAAA | 57626 |
rs9599506 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747514 | agaatcggattcatt[A/G]cagtcactcagtTTT | 57626 |
rs9599508 | snp | A/T | 0.439502 | 0.163061 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752161 | TTATATCAGTATTCA[A/T]TATGTTGAAGATTAT | 57626 |
rs9599509 | snp | C/T | 0.381308 | 0.21274 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752485 | ATTTCATGTGGTACG[C/T]AGACATTGTTTTAAA | 57626 |
rs9599511 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69766495 | atacatatatatata[C/T]atTTAGAGTGCTTGA | 57626 |
rs9599512 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69791073 | CACACACATAAAAAa[A/G]aaaaaataataataa | 57626 |
rs9599513 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69791074 | ACACACATAAAAAAG[A/G]Aaaaataataataaa | 57626 |
rs9599515 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69815961 | AGAAATATGAAAAGG[C/G]TATATTTTGTTGGTA | 57626 |
rs9599517 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861102 | TGAACTGTTTTAGAA[A/G]TGGCCAAAGTAACGC | 57626 |
rs9599520 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882102 | AGCGGCAGAGATAGG[A/T]TTTAGATCCACGATC | 57626 |
rs9599521 | snp | G/T | 0.128976 | 0.218754 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890102 | ACTTTCTAGTGAGGG[G/T]GACAGTATAGTATTA | 57626 |
rs9599522 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69913957 | ctgggtgagcacaat[C/G]taatcaactgccagt | 57626 |
rs9599523 | snp | A/C | 0.348574 | 0.229746 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914846 | AATCTATCAAGCTGG[A/C]AGCAAAATAGATAAA | 57626 |
rs9599524 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925354 | agttaatataatata[C/T]gtaaaacacttagaa | 57626 |
rs9599525 | snp | A/G | 0.424968 | 0.178567 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939272 | AATTTAAACTGTACA[A/G]TTGAAATGGCTTTTA | 57626 |
rs9599526 | snp | C/T | 0.386313 | 0.209568 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981747 | ATTTTAAACAACATA[C/T]AGTCATTTTTACAAA | 57626 |
rs9599527 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69983108 | caatcccatttatat[C/G]tattttaaagaccct | 57626 |
rs9599528 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996885 | AGAAATTGCCTTTAT[C/G]AAAAGTTCTTATTTT | 57626 |
rs9599531 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018490 | GAAATCTATGAAGAT[C/T]AGTACCTGATTTAGA | 57626 |
rs9599532 | snp | C/G | 0.421368 | 0.182025 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019420 | TTGAGTACTTTTTCA[C/G]CAGCTAGCTTCACTT | 57626 |
rs9599533 | snp | G/T | 0.420574 | 0.182769 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024376 | ATAGAGAGTGAGAAA[G/T]GGGGAAGAGAGAGAG | 57626 |
rs9599534 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024638 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 57626 |
rs9599535 | snp | G/T | 0.42803 | 0.175514 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027652 | CGCAAAATGTAAGTT[G/T]TTTTTTTTTTTTTAT | 57626 |
rs9599536 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030145 | cacacaataataatg[A/G]gagactttaacaccc | 57626 |
rs9599538 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70045923 | CCTATGCCTGAAAAT[G/T]GCCTCATCCTGGTAA | 57626 |
rs9599539 | snp | C/T | 0.417034 | 0.18601 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055227 | ccggcagctgactta[C/T]cagtgagaacctcac | 57626 |
rs9599541 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057093 | aaataaaattagaga[A/T]aaaaaaacattacaa | 57626 |
rs9599542 | snp | A/G | 0.4231 | 0.180378 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068194 | AAAATACAAAAAATT[A/G]GCCGGGCGTGGTGGC | 57626 |
rs9599544 | snp | A/T | 0.277867 | 0.248442 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085024 | TACCATCCATTGATG[A/T]CATGAATATGGTAAA | 57626 |
rs9599545 | snp | C/T | 0.366266 | 0.221319 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088535 | ATAAACTTGTGAAAC[C/T]AGCTGGGCATGTTGG | 57626 |
rs9599546 | snp | A/G | 0.256897 | 0.249905 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092557 | ATTATTAGATACAAA[A/G]TTTAATTAATGAAAA | 57626 |
rs9599547 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096020 | ttgttgcaattaaca[A/T]gatttcattcgtttt | 57626 |
rs9599548 | snp | C/T | 0.274661 | 0.248781 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099223 | TACTATTATTCAAGA[C/T]GTTCTATATAAGTAA | 57626 |
rs9634958 | snp | A/G | 0.401392 | 0.198948 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809093 | atctatgatattagc[A/G]tacctgggagagaag | 57626 |
rs9634959 | snp | A/G | 0.461703 | 0.132974 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809100 | atattagcgtacctg[A/G]gagagaagaggaagc | 57626 |
rs9634960 | snp | C/T | 0.461481 | 0.133325 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809785 | aataacaagacccat[C/T]cttccactgtcttcc | 57626 |
rs9634961 | snp | A/G | 0.391397 | 0.206172 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810584 | tacatcgagaagata[A/G]aaatatctcaaatta | 57626 |
rs9634962 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840163 | AATTAAAATGTGTAA[C/G]CCTACCTAATATATA | 57626 |
rs9634963 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840219 | TATAGAAACACATAA[C/G]ATACACAGTATAAtt | 57626 |
rs9634964 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69842014 | aaactagactcctat[C/G]tgtcaccatatacaa | 57626 |
rs9634965 | snp | G/T | 0.325091 | 0.238456 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024098 | TACGAGATCAGAGGA[G/T]ATCGGGCACATTCAG | 57626 |
rs9634966 | snp | G/T | 0.315273 | 0.241329 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070111 | aggcagaggttgcag[G/T]gagccgagtccagcc | 57626 |
rs9634967 | snp | C/T | 0.290977 | 0.246619 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094819 | CAGCCTTTTTCTAAC[C/T]ACCTGTGTTTCCTCT | 57626 |
rs9634968 | snp | A/G | 0.317933 | 0.240593 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102933 | AGAATGATGAGTAAA[A/G]CAGACATACTCCTCT | 57626 |
rs9645952 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749895 | AATATATTCTAAGCT[C/G]TAAACAGTTTCAATA | 57626 |
rs9646064 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770203 | tgccagcacccaagg[G/T]gaaagccagtcttgg | 57626 |
rs9741030 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935218 | TTGGTACTGGTGAAC[G/T]TGGTACATAGTTCAC | 57626 |
rs9741033 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935263 | GGTACATAGTTCACC[C/T]ACTGGTGAACTTGGT | 57626 |
rs9783531 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764723 | atttagaaatgcaga[A/G]tacctctcaacacag | 57626 |
rs9783559 | snp | A/T | 0.455977 | 0.141681 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764754 | atcgactcaattcta[A/T]tctgaattttaagaa | 57626 |
rs9788338 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69956005 | ttatttgatatatat[A/T]tatatatatttgata | 57626 |
rs9788380 | snp | C/T | 0.322245 | 0.239334 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791985 | aagaaaattgcagag[C/T]gtcaggagaaatagc | 57626 |
rs9788391 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69956007 | atttgatatatattt[A/T]tatatatttgatata | 57626 |
rs9788409 | snp | C/T | 0.327211 | 0.237778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955848 | TTGTTTTGCTCCATT[C/T]TTAAATGAGAAAATA | 57626 |
rs9805203 | snp | A/G | 0.4444 | 0.15719 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717640 | AAATATCATTTCATT[A/G]GCAGCATTTATATAA | 57626 |
rs9989055 | snp | A/T | 0.277334 | 0.248501 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979179 | GGCTCAAAAAAAAAA[A/T]AAATAAGTTCCAGTT | 57626 |
rs9989090 | snp | A/G | 0.48546 | 0.0840147 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979247 | AAGTTTCTTCATATT[A/G]TATCTGAGAACACAT | 57626 |
rs9989091 | snp | A/C | 0.490231 | 0.0692021 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979390 | ATCTTTCTCCTCAAC[A/C]TTATACTTAATATAG | 57626 |
rs10047674 | snp | C/T | 0.372794 | 0.217765 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748559 | ATTATGGGAGTATAA[C/T]TCAAGATGAGATTTG | 57626 |
rs10161795 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960156 | TTTACTGAGTGTTAT[C/T]TTAGTGTTAGCAAAT | 57626 |
rs10507772 | snp | G/T | 0.465892 | 0.126058 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801017 | ACCTACAAGGTGAAG[G/T]CGAATTACTCTGTGC | 57626 |
rs10507773 | snp | C/T | 0.118235 | 0.212457 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819752 | CTTAGGATTTCCTTA[C/T]CTAGGCTCTGCTTTT | 57626 |
rs10507774 | snp | A/C | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882630 | ACTCGATCCTTCAGA[A/C]ACTAGAGGCTGTTAA | 57626 |
rs10507775 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913006 | AATGATATTTTTGTC[A/G]TCAACAAGCAAGGCT | 57626 |
rs10507776 | snp | G/T | 0.25045 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979645 | AAACTTTACAGTTTC[G/T]TTCCAATCGAAGAGT | 57626 |
rs10507777 | snp | C/T | 0.234401 | 0.249513 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008046 | TATTTTGATGATTGG[C/T]TCTTACTATTTGGTT | 57626 |
rs10507778 | snp | G/T | 0.234401 | 0.249513 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008860 | TCATTGATTTAGAAA[G/T]TTGTACACTTGTAAT | 57626 |
rs10542087 | in-del | -/TCTATCTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789018 | TGGACTCCACAGGAC[-/TCTATCTA]TCTATCTATCTATCT | 57626 |
rs10542094 | in-del | -/AA | 0.089084 | 0.191327 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846737 | TTGAACCACATGATC[-/AA]AATAGTCACATGTTT | 57626 |
rs10542971 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69851210 | tttttataaaattct[G/T]ttatttataattaCA | 57626 |
rs10549532 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69996911 | TTTTTTTTTTTTTTT[-/T]GGCTGGCACAGTGAC | 57626 |
rs10555675 | in-del | -/CTT | 0.475081 | 0.108804 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101270 | AAATACAATATTGTC[-/CTT]CAACTAGCATGTTTC | 57626 |
rs10565530 | in-del | -/GA | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825633 | TGGAGAGAGACTGGA[-/GA]TAGGGAGATCACTGT | 57626 |
rs10597615 | in-del | -/AAAAT | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904165 | TCATTTAATAATAGA[-/AAAAT]AAAATGCATTAAGTT | 57626 |
rs10608243 | in-del | -/A | 0.237014 | 0.249662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743825 | AAAACAAAAAAACAG[-/A]AAAAAAAAAAAAACA | 57626 |
rs10632451 | in-del | -/TTTG | 0.475877 | 0.107142 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961828 | AGATTTCTATTATGT[-/TTTG]TTTATTTGCCTGTTC | 57626 |
rs10633347 | in-del | -/ACT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851108 | ACATACATATATACT[-/ACT]TTTATTTTTTATGCT | 57626 |
rs10633348 | in-del | -/AACT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851154 | CTTTTTTTAAGTACT[-/AACT]GTGTTTACTTAAATT | 57626 |
rs10639117 | in-del | -/A/AA | 0.124491 | 0.216211 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007444 | GCAATATTTCATCTC[-/A/AA]AAAAAAAAAAACACA | 57626 |
rs10641171 | in-del | -/TATT | 0.451608 | 0.147832 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781910 | TTTCCCATAATTTAA[-/TATT]TAGTCATTTTATTGC | 57626 |
rs10667717 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027652 | TGTTTTTTTTTTTTT[-/T]ATGAACTGAACAAAA | 57626 |
rs10669137 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69955944 | ATATTTGATATATAT[A/T]TATATATATATTTGA | 57626 |
rs10670182 | in-del | -/T | 0.313814 | 0.241719 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086708 | ACTTTTTTTTTTTTT[-/T]CAAATCTTACCTCTT | 57626 |
rs10676959 | in-del | -/ATT | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881746 | GGCTTCTTAACTCCA[-/ATT]ATTACATATTCCATA | 57626 |
rs10691528 | in-del | -/A | 0.225332 | 0.252724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088855 | ACTCATCAGAAAAAG[-/A]AAAAAAAAACTTATC | 57626 |
rs10694173 | in-del | -/ACTA | 0.123452 | 0.215605 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851151 | GTCTCTTTTTTAAGT[-/ACTA]ACTGTGTTTACTTAA | 57626 |
rs10706639 | in-del | -/A | 0.213937 | 0.247385 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022811 | CCTAAGCCTTTTTTT[-/A]ATGCCTTAATCTCAT | 57626 |
rs10717768 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911569 | AGGAATATCATCAAG[-/A]AAAAAAAAAAAAAAG | 57626 |
rs10719197 | in-del | -/A | 0.31829 | 0.240492 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031116 | AATAGCCTGCCAACC[-/A]AAAAAAAACCCAGAT | 57626 |
rs11148828 | snp | A/G | 0.456214 | 0.141336 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792442 | ctgatacccttatac[A/G]ttgctggtgtgaaca | 57626 |
rs11148829 | snp | A/C | 0.427879 | 0.175668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810000 | gaagactcaactatt[A/C]taaatatatatgccc | 57626 |
rs11148832 | snp | A/G | 0.454664 | 0.143571 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991736 | ACCAGAAGTGCAAAG[A/G]GGAGCATTCCTACTG | 57626 |
rs11278699 | in-del | -/GGGTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70061394 | ATTTTCTTTTATTTT[-/GGGTTT]AAGTGGTTTTTACTG | 57626 |
rs11296959 | in-del | -/A | 0.371785 | 0.218331 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026856 | AACAAAGTATATATT[-/A]AAAAAAGACAAATAG | 57626 |
rs11313559 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825990 | AATACTTACTTACAG[-/A]AAAAAAAAGATTTAT | 57626 |
rs11335045 | in-del | -/A | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838135 | GCAGCTACAATTTTG[-/A]AATCTCAGTTCACAG | 57626 |
rs11336815 | in-del | -/A | 0.121016 | 0.214157 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719584 | GAATACAACCTAAAA[-/A]CACAATTGGAAAAAT | 57626 |
rs11338325 | snp | A/T | 0.19996 | 0.244941 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022811 | CCTAAGCCTTTTTTT[A/T]ATGCCTTAATCTCAT | 57626 |
rs11346374 | in-del | -/C | 0.105569 | 0.204058 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015662 | TGCTGGATGATTTTG[-/C]CCAACTGTAGGGTGA | 57626 |
rs11353006 | in-del | -/A | 0.36021 | 0.224397 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890239 | GCAATAACAATTTCC[-/A]AAAAAAGAAAATGTT | 57626 |
rs11357077 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847405 | TAATACTGCATTAGC[-/A]AAAAAAAAAAAAAAA | 57626 |
rs11362161 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69851141 | TATAGGTAGCTGTCT[C/T]TTTTTTAAGTACTGT | 57626 |
rs11372220 | in-del | -/G | 0.304188 | 0.244057 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826781 | AGTTGTTTTTTTCAT[-/G]TAAATAATGTGTTCT | 57626 |
rs11374810 | in-del | -/T/TT | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793498 | GTAAGTTTTTTTTTT[-/T/TT]ACATAAATCAAAGGG | 57626 |
rs11381687 | in-del | -/A | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729517 | TAGCAAAACAAGGGG[-/A]AAAAAATCACGTCAG | 57626 |
rs11383566 | in-del | -/A/AAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068045 | CGTTTTAGTATAAGT[-/A/AAA]AAAAAAAAAAAAAGG | 57626 |
rs11390324 | in-del | -/A | 0.139564 | 0.224285 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007604 | TTAAAGGGAAATGCT[-/A]AAAAATAGTCATGGG | 57626 |
rs11405654 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969941 | ATCGATTAAACTTTT[-/G]TAAGTTCCACTTCAA | 57626 |
rs11418677 | in-del | -/A | 0.459347 | 0.136653 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803303 | TCAATTTTACATAAT[-/A]AAAAACAAATTACAG | 57626 |
rs11433328 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69979168 | TTAGATAAGAGGCTC[-/A]AAAAAAAAAATAAAT | 57626 |
rs11438060 | in-del | -/G | 0.310386 | 0.242597 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929133 | TTTGTAGAATCATAA[-/G]GCTGCAAAGAACCAC | 57626 |
rs11454973 | in-del | -/T | 0.0433465 | 0.140692 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878242 | TCCTGGAAACATCTG[-/T]TTTTTTTTTATTTAT | 57626 |
rs11459436 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69895720 | TTTTTTCCTTTTTTT[-/T]TTTTTTCAAGGTCTT | 57626 |
rs11616357 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965723 | aaaaagtcttgaagt[A/G]aattaaaagtgctac | 57626 |
rs11616799 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954782 | CAAATTAGTTTCATA[C/T]GATAGTACTAAATGT | 57626 |
rs11617036 | snp | C/T | 0.40853 | 0.193309 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816143 | GTAGATTAGAAGATA[C/T]ATAATTTTGATGTTC | 57626 |
rs11617163 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781307 | ttttttttttttttG[A/T]CAAATATCAAGTTCA | 57626 |
rs11617171 | snp | A/G | 0.246485 | 0.249975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966013 | tgaagcagcaagtgg[A/G]ttggtgcaaaagtta | 57626 |
rs11617232 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895896 | attttttagtagaga[C/T]agggttttgccaggt | 57626 |
rs11617271 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69720486 | tccatgcactcaatt[C/G]tgctgaaacagggat | 57626 |
rs11618330 | snp | C/T | 0.443732 | 0.158012 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799416 | ATTTGGATTTCAAAG[C/T]CTCATTCAAATGAGC | 57626 |
rs11618357 | snp | A/G | 0.34526 | 0.23114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799529 | TACTCACTTATCCTA[A/G]TAGCTACAGCAGAAA | 57626 |
rs11618596 | snp | A/G | 0.245631 | 0.249962 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965797 | tctgaaatggagaaa[A/G]tgagtggtctgggca | 57626 |
rs11619211 | snp | A/C | 0.112631 | 0.208878 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960802 | AAATGTCAACATAGT[A/C]GATCAGAAAAAAAAA | 57626 |
rs11619708 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004381 | CATGAAATGCTAAGC[A/G]TCCAAGATTATGTTG | 57626 |
rs11619836 | snp | A/G | 0.40086 | 0.199352 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809744 | gatttaaaagacata[A/G]agaggtaaattggat | 57626 |
rs11620428 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781251 | TGAATCCTAACACTA[A/G]AATATGCTTCTTGAG | 57626 |
rs11620443 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957241 | CTAAACTGAGAATGC[C/T]AACAAGTAGATAGTG | 57626 |
rs11838519 | snp | C/T | 0.264358 | 0.249587 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987902 | TAAATGTAGAATAAA[C/T]TGCTACTTACAAACA | 57626 |
rs11838650 | snp | G/T | 0.490007 | 0.0699769 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034178 | AACTCAACATTTTAC[G/T]GTTGTCTATTAATCT | 57626 |
rs11838652 | snp | G/T | 0.489376 | 0.0721049 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034191 | ACTGTTGTCTATTAA[G/T]CTACATTTATTCTAA | 57626 |
rs11839323 | snp | C/T | 0.264632 | 0.249571 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990201 | atggaaagaccatta[C/T]cagccactatgaaac | 57626 |
rs11839721 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021317 | gcattaaagtgtctt[G/T]catggcttttcatgg | 57626 |
rs11839809 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715136 | ATTGTATCAGCTAAC[A/G]ATTGCTGCATCTACT | 57626 |
rs11839969 | snp | A/T | 0.246485 | 0.249975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987957 | AATtttctttttttt[A/T]aatttatcttttatt | 57626 |
rs11840536 | snp | A/G | 0.263809 | 0.249618 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993251 | ccagtgtctgggaga[A/G]ccatagcagaaccac | 57626 |
rs11840763 | snp | C/T | 0.265453 | 0.249522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989895 | ctagatatagaatca[C/T]gtaacttgtaaacag | 57626 |
rs11840776 | snp | C/T | 0.131038 | 0.219882 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990032 | tatattcaacattct[C/T]aaagaaaataaattc | 57626 |
rs11841068 | snp | A/T | 0.251014 | 0.249998 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982326 | ctgtagtcccagctg[A/T]ttgggagactgagac | 57626 |
rs11841250 | snp | C/G | | | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970627 | CAACTGCCACCACCT[C/G]TCCTGACTCTCAACC | 57626 |
rs11841320 | snp | A/G | 0.26518 | 0.249539 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988099 | ttttttggcgggggg[A/G]acctctccttcctcc | 57626 |
rs11842166 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69814675 | atgcaaatcaaaatc[A/C]caatgagatacctcc | 57626 |
rs11842167 | snp | A/G | 0.460589 | 0.13473 | intron-variant | KLHL1 | GRCh38.p7 | 13:69784604 | ggccattacataatg[A/G]taaagggatcaattc | 57626 |
rs11843309 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880828 | TAATTCCAAACTCCC[C/T]ACATTTCAACCAACA | 57626 |
rs11843787 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052150 | TAAGCAGCACAAATT[C/T]TGATGCACAGAAATT | 57626 |
rs11843928 | snp | C/T | 0.251014 | 0.249998 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982319 | tgtgcatctgtagtc[C/T]cagctgattgggaga | 57626 |
rs11843948 | snp | C/T | 0.114387 | 0.210022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917455 | gaattaagaaaaccc[C/T]cgtcccagtgagcac | 57626 |
rs12020157 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69955942 | atatatttgatatat[A/T]tttatatatatattt | 57626 |
rs12021017 | snp | G/T | 0.0741063 | 0.177655 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730511 | TAAAAAGGCAAAAAG[G/T]ATTATGCTTTCCTCT | 57626 |
rs12184611 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885836 | AAAAAGTGCAATTAT[C/T]TGGAAAATGATAGTA | 57626 |
rs12427517 | snp | A/T | 0.14665 | 0.227637 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778784 | TATTGAAGGCAGGTA[A/T]TCCCTCTCttttttt | 57626 |
rs12427812 | snp | C/T | 0.16911 | 0.236552 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774124 | ATAGTAACACAGCAG[C/T]ATTACTCTTTTTAAA | 57626 |
rs12427920 | snp | A/G | 0.298651 | 0.24522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859189 | AATACCTTCTGACTG[A/G]TGTATCTGCTCCCAT | 57626 |
rs12427924 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734840 | ATAAAACTTCTACTG[C/T]CATTTCTTTCTCATG | 57626 |
rs12427968 | snp | C/T | 0.464629 | 0.128197 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810011 | tattctaaatatata[C/T]gcccccaacattaaa | 57626 |
rs12428010 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847424 | AAAAAAAAAAAAAAA[A/T]AAACATAATTTAAAG | 57626 |
rs12428011 | snp | A/G | 0.114387 | 0.210022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847455 | GCAGGAAAATAGGAG[A/G]TGTACCAAGCGCAGC | 57626 |
rs12428036 | snp | A/G | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901974 | agctaatttttttgt[A/G]ttgttagcagagaca | 57626 |
rs12428088 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837622 | tctctctctatatat[A/G]tgtgtgtgtatatat | 57626 |
rs12428090 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837642 | tgtgtatatatatat[A/G]tgtgtatatatatat | 57626 |
rs12428263 | snp | C/G | 0.231189 | 0.249291 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820328 | taattacattaagca[C/G]aaattttactactaa | 57626 |
rs12428267 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820474 | gtttactctctgtct[C/T]ctagtgataagcttg | 57626 |
rs12428294 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026414 | AGTTTTAAGAACTCA[C/G]AAATACAGTGTGATT | 57626 |
rs12428493 | snp | C/T | 0.00470586 | 0.0482782 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817307 | TAGTATTCCTGATTG[C/T]ATGGCAAAAAAAGAA | 57626 |
rs12428566 | snp | C/G | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067727 | AAATAAACAATCAAT[C/G]AGACTTTCTAAGAGC | 57626 |
rs12428810 | snp | C/T | 0.482831 | 0.0910472 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788535 | GGGAGGTGGGAGGGA[C/T]AGCATTAGGAGATAT | 57626 |
rs12428998 | snp | A/G | 0.00995 | 0.0698283 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081678 | atcaatagagtttaa[A/G]caggaatttccattg | 57626 |
rs12429094 | snp | A/G | 0.453939 | 0.144598 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798602 | ATAATATTTTAAACA[A/G]ATGTATTTTATATTT | 57626 |
rs12429100 | snp | A/C | 0.140581 | 0.224783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798820 | cacctgtaatcccag[A/C]actttgtgaggccaa | 57626 |
rs12429374 | snp | G/T | 0.175897 | 0.238765 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820699 | CTGTTCAAGGGACAT[G/T]CAGGCCGAATTTGCT | 57626 |
rs12429407 | snp | C/G | 0.141258 | 0.225111 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799858 | gacgcacagcaggag[C/G]tgagcggcaccccga | 57626 |
rs12429437 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764232 | atcaactgttaaaac[C/T]atgtttaaataaggc | 57626 |
rs12429486 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882817 | TGGTGAATAGGAAAA[A/C]ATAACATTTCACATT | 57626 |
rs12429498 | snp | A/C | 0.144756 | 0.227146 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724124 | acagtcgtgagatac[A/C]gtgcctggctacgtg | 57626 |
rs12429555 | snp | A/G | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900321 | CTCATGAAACTTCAC[A/G]TTAAACACCAGCTTT | 57626 |
rs12429576 | snp | A/G | 0.084364 | 0.187256 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900468 | CAAAATGTGGATTTC[A/G]GATTAGCGTTTTTCA | 57626 |
rs12429752 | snp | A/C | 0.0592355 | 0.161582 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788561 | gatatgcctaatgct[A/C]aatgatgagttaatg | 57626 |
rs12429762 | snp | A/T | 0.0592355 | 0.161582 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788627 | gtaacaaacctgcac[A/T]ttgtgtacatgtacc | 57626 |
rs12429783 | snp | A/G | 0.151668 | 0.229849 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758753 | tttttttgtttactg[A/G]cagatctaattatat | 57626 |
rs12430131 | snp | C/T | 0.457271 | 0.139781 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798320 | TTACTCTTTAGAACC[C/T]AACTAGTAATGAACT | 57626 |
rs12430158 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837630 | TATATATATGTGTGT[A/G]TATATATATATATGT | 57626 |
rs12430159 | snp | A/G | 0.16976 | 0.236773 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837646 | tatatatatatatgt[A/G]tatatatatatgtgt | 57626 |
rs12430221 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802237 | ttccatggtgtatat[A/G]tgccccattttcttt | 57626 |
rs12430261 | snp | A/C | 0.0818113 | 0.184966 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073633 | attcttctaaaaacc[A/C]gggtgtggtggtgtg | 57626 |
rs12430318 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820543 | agggaattggccaac[A/G]gaggcataagcgtaa | 57626 |
rs12430410 | snp | A/T | 0.0861826 | 0.188849 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815716 | AATCTAAAATTTTTT[A/T]AAAAAGCCGTAAATG | 57626 |
rs12430504 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764327 | ttctgtacatcactt[C/T]cctttttctttccat | 57626 |
rs12430527 | snp | C/T | 0.301681 | 0.2446 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833824 | atatacacacacaca[C/T]atgtatacatatata | 57626 |
rs12431003 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081755 | ggcctagtgaaactt[C/T]gaagcagaagaccta | 57626 |
rs12431067 | snp | A/G | 0.249603 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828717 | caggctgatgctggg[A/G]caaggtgggaataag | 57626 |
rs12431120 | snp | A/G | 0.164219 | 0.234823 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823368 | TTCAATTTTATTAAA[A/G]TAAGTGAATATCATG | 57626 |
rs12431195 | snp | C/T | 0.437259 | 0.165632 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801987 | CATCTAGGTTTTAAG[C/T]CCCACATGCATTAAG | 57626 |
rs12431235 | snp | C/T | 0.398894 | 0.200825 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038346 | tttgcctattacaaa[C/T]aatgctgttatgaac | 57626 |
rs12431330 | snp | A/C | 0.454061 | 0.144427 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799642 | AGTGACAAATAACAC[A/C]GATTTGTTATCTTAC | 57626 |
rs12431347 | snp | A/C | 0.453818 | 0.144769 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799795 | GAACAAGGGTCCCCA[A/C]CTTCCAGGACGTGGA | 57626 |
rs12583014 | snp | A/T | 0.462363 | 0.131916 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794466 | AACAGAGCATCTTAA[A/T]GGTGGGAGAGAGGAA | 57626 |
rs12583490 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780707 | atatatatatgtata[C/T]atatatatgtatata | 57626 |
rs12584120 | snp | A/C | 0.457271 | 0.139781 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797763 | GAACCCGGGAGGCGG[A/C]GCTTGCAGTGAGCAG | 57626 |
rs12584126 | snp | C/T | 0.360421 | 0.224293 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797858 | AAATCTGGGGAATAG[C/T]TTAATAGAATTTTAT | 57626 |
rs12584317 | snp | G/T | 0.393803 | 0.204501 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759313 | TTTGACAGcattagc[G/T]catgaacaaatcaag | 57626 |
rs12584420 | snp | C/T | 0.031825 | 0.122064 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064767 | GATTTGGCTGGCGAT[C/T]CACGACTAAGGACTA | 57626 |
rs12584568 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855345 | agatagatagataga[C/G/T]agacagacagataga | 57626 |
rs12584685 | snp | A/G | 0.4021 | 0.198407 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812197 | ggttgttcagtttcc[A/G]tgcaattgagcggtt | 57626 |
rs12585039 | snp | A/C | 0.456095 | 0.141508 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759035 | aaattaagggcaggg[A/C]ttgtctatgtccaga | 57626 |
rs12585046 | snp | A/G | 0.368324 | 0.220226 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759105 | tcccagcagggaggc[A/G]aatctgggccgagga | 57626 |
rs12585117 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807057 | agtttaatactgggc[A/C]gagttttgcctttgg | 57626 |
rs12853291 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69778552 | TAGTTCTTGATTGTA[C/T]AAGAGATATCTATGG | 57626 |
rs12853326 | snp | G/T | 0.403158 | 0.197592 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061784 | GTGTTTATTTATTTT[G/T]GGCTTATCTTTTTTA | 57626 |
rs12853504 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69778406 | AAAGGTATGCTATAG[A/G]CTTTCAGCATCTTAT | 57626 |
rs12853901 | snp | C/T | 0.373397 | 0.217424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864597 | ATTTTTCAAATATAG[C/T]TACTGGTTCAAAAAA | 57626 |
rs12855970 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69841879 | gagaggccagaaata[A/C]agccacgtatttact | 57626 |
rs12856844 | snp | C/T | 0.1652 | 0.235179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832892 | attttgttgggataa[C/T]tggcaagccacatgg | 57626 |
rs12856926 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69841881 | gaggccagaaataaa[C/G]ccacgtatttactgc | 57626 |
rs12857338 | snp | A/G | 0.160938 | 0.233598 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841998 | cacatgcagaagaat[A/G]aaactagactcctat | 57626 |
rs12857374 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69869910 | AATGATTATTACAAA[A/T]AATACTACAATGGAA | 57626 |
rs12857376 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869911 | ATGATTATTACAAAA[A/G]ATACTACAATGGAAG | 57626 |
rs12858688 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782332 | ggtcagtgggtgcag[C/T]gcaccgtgtgctagc | 57626 |
rs12859720 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782376 | ggcattgcctcactc[A/G]ggaagcgcaaggggt | 57626 |
rs12861094 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027291 | ACAAAGTAAGAAGCC[A/C]CGGAGATATAATGAC | 57626 |
rs12861097 | snp | A/T | 0.366885 | 0.220993 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842401 | gactaggtatttctc[A/T]aaagaaaacatacaa | 57626 |
rs12863124 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865366 | TTTTCAAAAGGCTAT[A/T]TTGCTTTCTACAAGT | 57626 |
rs12863245 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69996939 | ttttttttttttttt[G/T]GGCTggcacagtgac | 57626 |
rs12863769 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721042 | cctcccattctattc[A/C]tagaaaagatagcta | 57626 |
rs12864305 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721045 | cccattctattccta[C/G]aaaagatagctacta | 57626 |
rs12864499 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770669 | GTGGAAATGAACTGA[A/G]TGAGAGAGATGGAAG | 57626 |
rs12864769 | snp | G/T | 0.369754 | 0.219451 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079911 | GTGAAGAGTTTTTTA[G/T]AACTGAATCATTTTT | 57626 |
rs12865460 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001242 | AGCTAAGAATAATTA[A/G]AAATAAAAATGTAGT | 57626 |
rs12865870 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936444 | aaatacaaaaattag[A/C]caggtgtggtgacag | 57626 |
rs12865877 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936495 | ttgggagtctgggac[A/G]ggagaattgcccgaa | 57626 |
rs12865902 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936541 | ttgcagtgagtggag[A/G]ttacgcctctgcact | 57626 |
rs12865944 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70036836 | TTTAATGCCATGGTC[C/G/T]ttttttttttttttt | 57626 |
rs12865991 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69764921 | TCATGCTTTCATGTA[A/T]ATCTTTGCTTTTTTT | 57626 |
rs12866143 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936443 | aaaatacaaaaatta[A/G]ccaggtgtggtgaca | 57626 |
rs12866296 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709346 | CAGAAAAtaaaagat[A/C]ccacaagggagaaaa | 57626 |
rs12866299 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69709349 | AAAAtaaaagatacc[A/C]caagggagaaaatag | 57626 |
rs12866333 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936560 | cgcctctgcactcca[C/G]cctaggtgacagaca | 57626 |
rs12866998 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075571 | tgtgtgtgtatgtgt[A/G]tatatatatatatat | 57626 |
rs12866999 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075573 | tgtgtgtatgtgtat[A/G]tatatatatatatat | 57626 |
rs12867035 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075634 | tatatatatgtatat[A/G]tatataggactttta | 57626 |
rs12867044 | snp | A/T | 0.435407 | 0.167703 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862599 | TGTTGCTATGTACTG[A/T]ATTGTGTCCCCTCAA | 57626 |
rs12867150 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936477 | gcctgtagtcccagt[C/T]acttgggagtctggg | 57626 |
rs12867164 | snp | C/T | 0.435407 | 0.167703 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862589 | GTTTTATACCTGTTG[C/T]TATGTACTGAATTGT | 57626 |
rs12867326 | snp | A/G | 0.00732591 | 0.0600773 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075791 | tatatatgtatatat[A/G]tatGttgcaggatat | 57626 |
rs12867330 | snp | C/T | 0.375 | 0.216506 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075758 | atacacacatacaca[C/T]acatatatatatata | 57626 |
rs12867434 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075628 | cttacatatatatat[A/G]tatatatatatagga | 57626 |
rs12867534 | snp | C/T | 0.435263 | 0.167862 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862826 | AAGCCAGGAAGAAAG[C/T]CCTCACCAGCAACTA | 57626 |
rs12867655 | snp | C/G | 0.435263 | 0.167862 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862754 | GAGAGATCTCTCTCT[C/G]TTTGTTTCTTCAGAG | 57626 |
rs12867754 | snp | C/T | 0.368938 | 0.219895 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709439 | GCAAAAGATAAAGAG[C/T]AAATAATTAGGAAGA | 57626 |
rs12867774 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075783 | tatatacatatatat[A/G]tatatatatatGttg | 57626 |
rs12868155 | snp | C/T | 0.435407 | 0.167703 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862540 | ACTCATTAAAGTAAG[C/T]GTAAGGCAAATATAA | 57626 |
rs12868282 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075602 | atacacacacacaca[C/T]atatataggacttac | 57626 |
rs12868283 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075604 | acacacacacacata[C/T]atataggacttacat | 57626 |
rs12868290 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075621 | tataggacttacata[C/T]atatatgtatatata | 57626 |
rs12868556 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075782 | atatatacatatata[C/T]gtatatatatatGtt | 57626 |
rs12868879 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70035676 | GGGAAAGGAGACTGA[A/G]GTAGTTTTGGTAATC | 57626 |
rs12869055 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70093040 | ttatttttaaaGACA[G/T]TGAATAACATTAATG | 57626 |
rs12869057 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70093041 | tatttttaaaGACAT[G/T]GAATAACATTAATGA | 57626 |
rs12869109 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084623 | gccaccacgccaggc[C/T]ttttttttttttttt | 57626 |
rs12869750 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69963085 | Attttttttagagac[A/T]gtatctctttctgtt | 57626 |
rs12869914 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007745 | TTTAAAAAATCATAA[A/C]CCATAATTATTCACT | 57626 |
rs12869925 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007766 | ATTATTCACTAAAAC[A/C]CAGAACAAGAAAACA | 57626 |
rs12870676 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69840702 | tatatatatatatat[A/G]tatgtatgtatgtat | 57626 |
rs12870797 | snp | A/C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69867881 | gggggagggatagca[A/C/T]taggagatataccta | 57626 |
rs12870969 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69963093 | tagagacagtatctc[C/T]ttctgttgtctagga | 57626 |
rs12871523 | snp | A/C | 0.400325 | 0.199756 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060454 | aatattttaaagaca[A/C]acctgccctcccatg | 57626 |
rs12872359 | snp | C/T | 0.43555 | 0.167544 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862907 | ATACATTTCTGATGT[C/T]TAAGCCACCCAGTCT | 57626 |
rs12873728 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099751 | AGTTGTTAATTAAAC[C/T]AAGATTAAACATTAG | 57626 |
rs12874502 | snp | A/G | 0.397813 | 0.201621 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057705 | ggcgtgaacccggga[A/G]gcggagcttgcagtg | 57626 |
rs12875147 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841621 | aatatcattaaaatg[A/C]ccgcattgctcaaat | 57626 |
rs12875306 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69841702 | cacagaattggataa[A/C]caattctaaaatata | 57626 |
rs12875319 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841731 | tatataaaacatcaa[A/C]ccaaaaaagagccca | 57626 |
rs12875590 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060907 | cagctataaaaaaag[A/G]acaagatcctgtcat | 57626 |
rs12875608 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060961 | agggacactatgtta[A/G]cagaaatatgccagg | 57626 |
rs12875710 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060980 | aaatatgccaggcac[A/C]caaagactaagttca | 57626 |
rs12875833 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060981 | aatatgccaggcaca[A/C]aaagactaagttcag | 57626 |
rs12875952 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69987747 | CTTAGAGTAAAATAC[A/C]CAGATAAAAATAGAA | 57626 |
rs12875988 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869817 | GGAATATTTTAAATT[A/T]CAGAAGTTGTAAACT | 57626 |
rs12876159 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781289 | tttttttctttcttt[C/T]ttttttttttttttt | 57626 |
rs12876582 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024678 | tctggctctgtctct[C/T]tttctttctttattt | 57626 |
rs12877094 | snp | A/T | 0.43555 | 0.167544 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864612 | TTACTGGTTCAAAAA[A/T]ATTCCATACTCACAA | 57626 |
rs12877491 | snp | G/T | 0.248755 | 0.249997 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829226 | ctactacctccgctg[G/T]tgtgtatggctgaga | 57626 |
rs12877706 | snp | C/G | 0.47666 | 0.105476 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100819 | ATTTGTTTTTTACAA[C/G]TACCACAAACATACC | 57626 |
rs12877925 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69778556 | TCTTGATTGTACAAG[A/T]GATATCTATGGATTT | 57626 |
rs13378913 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870868 | gggctctcatggtct[C/T]gtggttttgcttggt | 57626 |
rs13378978 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69916702 | gtatgtaacaaacct[A/G]cacattgtgcacatg | 57626 |
rs17070795 | snp | C/G | 0.079617 | 0.182947 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750260 | GTCATCGTGTATAAA[C/G]TATCACCCAGTAAAT | 57626 |
rs17070810 | snp | A/G | 0.16911 | 0.236552 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775811 | TTCTCCTTCCACGTC[A/G]CGGAAAGGGGCTCTC | 57626 |
rs17085272 | snp | A/G | 0.280785 | 0.248097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705122 | CATGATAGTACTATG[A/G]CAGTATACCAAGATA | 57626 |
rs17085275 | snp | C/G | 0.367503 | 0.220665 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708873 | ATAAATTCTTAGTTT[C/G]TTTTCCTGCTCCAAT | 57626 |
rs17085319 | snp | A/T | 0.106278 | 0.204558 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752226 | CAAGCTTCAGTCTAT[A/T]GTATCACTGTAGAGA | 57626 |
rs17085322 | snp | G/T | 0.106278 | 0.204558 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752300 | TTGCTAATGCACCCC[G/T]TTGCCTCTATTTCTG | 57626 |
rs17085328 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753670 | CAATCATTGGCAAAA[A/C]CATTAAAAATTCAGT | 57626 |
rs17085330 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753779 | TACACAGGATTCCGT[C/G]TATACCAATATTAGC | 57626 |
rs17085337 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760286 | CCTTTTGTAAACACC[C/T]TATCCAGAATTATTT | 57626 |
rs17085346 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762257 | ATTAACTGAATTTTC[C/T]TGGTCAAAGGTATTG | 57626 |
rs17085354 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765502 | AATGAGAGTCAATAC[C/T]AGGTAATATTAAAAA | 57626 |
rs17085356 | snp | A/G/T | 0.031566 | 0.122372 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766028 | TTTGTAGATGATACC[A/G/T]AAATCTTCAGCAATC | 57626 |
rs17085369 | snp | C/G | 0.127254 | 0.217792 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773340 | ATGAATAGTCAGAAA[C/G]TCTGATCAAGCATCA | 57626 |
rs17085372 | snp | A/G | 0.16911 | 0.236552 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773776 | ATTTAGTGTTCTGTT[A/G]CTCTATTACATGCAA | 57626 |
rs17085375 | snp | A/G/T | 0.14665 | 0.227637 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775284 | TTGGTCAATTGTCAT[A/G/T]AAAAAAAGAGGTACT | 57626 |
rs17085391 | snp | C/T | 0.140581 | 0.224783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794250 | AAGTCAGCTTACAGG[C/T]TTAGGGCTTCATGCC | 57626 |
rs17085396 | snp | C/G | 0.461813 | 0.132798 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797314 | GTAGCATAATACCAG[C/G]TTGAAAAATATTTAT | 57626 |
rs17085397 | snp | C/T | 0.141596 | 0.225274 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799345 | AGGAATGAGTGAAAT[C/T]AAGACTTCCGAGCAA | 57626 |
rs17085403 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801445 | ATCCACATTGTTTTT[C/T]CTCTTAAACTCAAGA | 57626 |
rs17085405 | snp | A/G | 0.118584 | 0.212673 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801763 | TTTATTATAGACTAT[A/G]TGTTAGTTAAGAGAT | 57626 |
rs17085438 | snp | A/C | 0.0759472 | 0.179459 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820865 | ACGTTTGGCACTAGA[A/C]ATTTCCAAGAAAAAT | 57626 |
rs17085439 | snp | C/T | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823064 | GTGAAGACATAGAAG[C/T]CTCACCTCCGATGGA | 57626 |
rs17085441 | snp | A/G | 0.14933 | 0.228835 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823084 | CCTCCGATGGATAGA[A/G]GTTTAAGTGTGAAAG | 57626 |
rs17085443 | snp | A/G | 0.1652 | 0.235179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823252 | CCTCAAAATGTCTCA[A/G]AGAAATAGGAAATGT | 57626 |
rs17085444 | snp | A/T | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823302 | ATGAGAAACACCAAC[A/T]TTTAAAATACTTAAT | 57626 |
rs17085527 | snp | A/G | 0.319856 | 0.240042 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854661 | AGTTTCTCTGAAATT[A/G]TAAATGCTGCTTATT | 57626 |
rs17085529 | snp | A/C | 0.319856 | 0.240042 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854761 | TATAATTGGTTCTTA[A/C]ATAGTCTTTTGAATA | 57626 |
rs17085532 | snp | C/T | 0.438946 | 0.163706 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857088 | AAAACTCTCCGTTTT[C/T]TGTCTCCTAATTCTT | 57626 |
rs17085534 | snp | G/T | 0.428786 | 0.174744 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857152 | CTATGCTGTAGATTT[G/T]CCAAACACCTTGTAA | 57626 |
rs17085536 | snp | C/T | 0.436123 | 0.166908 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857669 | ATCATAAGTTGAATG[C/T]TTGTTCTCTGAAGTA | 57626 |
rs17085537 | snp | C/T | 0.435837 | 0.167226 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858152 | GGGGACACCCAGAGA[C/T]ATTTCAGCCATGTCG | 57626 |
rs17085538 | snp | A/T | 0.438246 | 0.16451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858248 | GCCTCTTCCTTCAAC[A/T]GACACCCTCTTGGGG | 57626 |
rs17085541 | snp | A/G | 0.435694 | 0.167385 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858764 | AAACACTTTCAGCAG[A/G]AGGTCTTGCATAAAC | 57626 |
rs17085550 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862520 | ATTACCACTGGATCA[C/T]CACAACTCATTAAAG | 57626 |
rs17085565 | snp | A/G | 0.311859 | 0.242226 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868114 | CTTTTCTTGATTTTG[A/G]TTAAATACTTGACTT | 57626 |
rs17085566 | snp | A/G | 0.284209 | 0.247648 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868417 | ATGACATGGACATAC[A/G]TTTTTTTAGATGATG | 57626 |
rs17085568 | snp | C/T | 0.316968 | 0.240864 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868763 | CACATGAATAAAATG[C/T]TGTTTTAGAGTTTGG | 57626 |
rs17085570 | snp | C/T | 0.188316 | 0.242271 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874983 | TTTTTTGTAATTTGT[C/T]TCTACATAGCATTTG | 57626 |
rs17085574 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880646 | ACATCTCTGATCTGA[C/T]GTAACCATTTAATGA | 57626 |
rs17085577 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880928 | ACTGATAACTATCAT[C/T]GGCTTTCTGGCTAAT | 57626 |
rs17085587 | snp | A/T | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882064 | GATATTATCATAATC[A/T]TACAAGTGGCCATGA | 57626 |
rs17085588 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882089 | CCATGAGTCAATAAG[C/T]GGCAGAGATAGGATT | 57626 |
rs17085591 | snp | A/C | 0.0970103 | 0.197722 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883525 | TGTAGTGGGTGTATC[A/C]CTGCCACAGCAGATA | 57626 |
rs17085594 | snp | A/C/T | 0.0934156 | 0.196197 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884377 | TGCCCATAACTGTTC[A/C/T]GGTAATTAACAAATT | 57626 |
rs17085595 | snp | A/G | 0.077417 | 0.180873 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884846 | ATTGAAATCTATCTC[A/G]TAGGAAGGCTATAGA | 57626 |
rs17085597 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885265 | TTTTATCTCTGCATC[C/T]AACTTAAATAATATT | 57626 |
rs17085598 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885324 | ACTAAATCTTTTGGT[A/G]ACCAGCGGCGTTGTT | 57626 |
rs17085600 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885645 | AGCAAACTCCTTATT[G/T]TCTATGAAGATCATA | 57626 |
rs17085605 | snp | A/C | 0.0916144 | 0.193427 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895293 | TACAAGAGGTTCACA[A/C]TTCTTTTCTTGTTTG | 57626 |
rs17085631 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897565 | ATTATTAAACCTAGC[A/G]AGGGACATTGGTTCC | 57626 |
rs17085638 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912821 | GTTCCTGAAGAGGCC[C/T]CATGCTGCTTGAGTC | 57626 |
rs17085643 | snp | C/T | 0.152001 | 0.229992 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913150 | AGGTCTCATACAGAT[C/T]AAGACCTTTTTGTTT | 57626 |
rs17085645 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917786 | TCACATAACATTCCA[C/T]GTATCTTTTGAAGTC | 57626 |
rs17085652 | snp | A/T | 0.0618563 | 0.164627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923677 | AAGGAGGAGAGTTAG[A/T]GAGAGACAATATAGT | 57626 |
rs17085666 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933115 | TTATACTCACCCTGA[C/G]CTTTTCATTTCATAT | 57626 |
rs17085671 | snp | C/T | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934300 | CTCTCTTTTTTATTT[C/T]TCAGTCTCCGAATAT | 57626 |
rs17085674 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934596 | ACTTGTTCAAAATGT[C/T]CAATGGCATATTATT | 57626 |
rs17085680 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934815 | ATGAACATTCTTTAA[C/T]CAAATCTACACCTGA | 57626 |
rs17085685 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934905 | CTGATTTATGGGAGG[A/G]TTCCCATTGCGTCTC | 57626 |
rs17085692 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935504 | AAAAAGGAGTGTAAG[A/G]GAATAGAGAGTTTTG | 57626 |
rs17085696 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935829 | TAAATTAAAGAAAGT[C/T]CTGCAAAAGTACCCA | 57626 |
rs17085700 | snp | A/C | 0.0752113 | 0.178743 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935876 | GATGAATGTATTACA[A/C]GATACTAGACACTTT | 57626 |
rs17085703 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936163 | GGATTCCAACAAGAG[A/G]AAGGTCTGAGTTAAG | 57626 |
rs17085706 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937579 | TTCAGTGCTGCTATT[C/T]TGGTGCTATCTCTAT | 57626 |
rs17085712 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937654 | ACACTTCTACCTGAT[A/G]CTGAGCTCGCAATCA | 57626 |
rs17085728 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947958 | GTTCTCAAATAAGCT[C/T]ACTAAAAGGGAAAAC | 57626 |
rs17085738 | snp | G/T | 0.31357 | 0.241783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948463 | AAACTGCTTATAAAA[G/T]TGGAGTCACCCTCCT | 57626 |
rs17085746 | snp | A/G | 0.31357 | 0.241783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948529 | TTAAATAGGGTTCCA[A/G]TAAGGTGTGCTACAT | 57626 |
rs17085756 | snp | A/G | 0.314301 | 0.241589 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956403 | ATTAGGCATTAATAT[A/G]CTTAAATTGTGAGGC | 57626 |
rs17085765 | snp | C/G | 0.314787 | 0.241459 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956593 | TGATACCCTATAAAA[C/G]TACACAAATCTGGTA | 57626 |
rs17085771 | snp | A/T | 0.327211 | 0.237778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956746 | GGCTTTGAATATATA[A/T]CTGTGTCCTCATATT | 57626 |
rs17085776 | snp | A/G | 0.314301 | 0.241589 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956768 | CCTCATATTAATTTA[A/G]AACAGACCAACACAT | 57626 |
rs17085785 | snp | C/T | 0.314544 | 0.241524 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957091 | CTGCCAAATCAAAGG[C/T]TTATTGAAGATTAAA | 57626 |
rs17085791 | snp | C/G | 0.314057 | 0.241654 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957468 | AAGTGATATGCATTC[C/G]CTATATTCCTTGATT | 57626 |
rs17085798 | snp | A/C | 0.326976 | 0.237854 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957697 | CCAACTAAGTATTTT[A/C]TTTACAACTTAAGAT | 57626 |
rs17085802 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957734 | TATAAAACGGCACTA[C/T]TTTATAACACACTCT | 57626 |
rs17085809 | snp | A/G | 0.314301 | 0.241589 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957884 | AATGACATGAACTTC[A/G]TATTAAGTTATAATT | 57626 |
rs17085815 | snp | C/G | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957912 | ATTATTTCTCTAACA[C/G]CAGTGTAAATTTTCT | 57626 |
rs17085818 | snp | A/C | 0.327211 | 0.237778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957965 | TGTGGGAAAAACTGA[A/C]CTTATGTTGTCGTTT | 57626 |
rs17085826 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958526 | TGTACTTTGTCCTTA[A/C]TTTCTAACTTAATAA | 57626 |
rs17085833 | snp | A/G | 0.16846 | 0.236329 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960052 | TATTAAGACCAAAAA[A/G]TGTCTAAGTATTTTC | 57626 |
rs17085855 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973106 | GAAATATATTAATGG[C/G]TTATCTGAAATATTA | 57626 |
rs17085949 | snp | A/G | 0.039522 | 0.134904 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976365 | ACAAAAAAGTAGAAT[A/G]TATTAACTCAGTACT | 57626 |
rs17085956 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976572 | AGACACATGATAAAG[C/T]CCAGCAGACCCAATC | 57626 |
rs17086026 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978164 | ATTCTTCCACCTGTT[A/C]ACGCATTGAATAGAA | 57626 |
rs17086031 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978188 | AATAGAAAAGTCACA[A/G]TATGCATTGCAGGGT | 57626 |
rs17086036 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978228 | GATTTAGAATGAACA[A/T]ACTATTGACTCTCAG | 57626 |
rs17086052 | snp | G/T | 0.44651 | 0.154543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978336 | CTTCTGCTTGGGTAC[G/T]CAGACTGCATGATTA | 57626 |
rs17086066 | snp | A/G | 0.250732 | 0.249999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979919 | AAGAATTGTCTTCAC[A/G]TCTTAACTTCAGTTC | 57626 |
rs17086073 | snp | G/T | 0.250732 | 0.249999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980328 | TATGACCTACCTACT[G/T]AGTGCAAATCTGAAA | 57626 |
rs17086079 | snp | A/C | 0.248471 | 0.249995 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980554 | ATCGCATTCCACACA[A/C]ATATTTTTCTGTACC | 57626 |
rs17086081 | snp | A/C | 0.25045 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980568 | ACATATTTTTCTGTA[A/C]CTGGAACCTGCACAA | 57626 |
rs17086082 | snp | C/T | 0.250732 | 0.249999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980654 | ACCTTCAGAAAGCCT[C/T]ATTTTTTTCAGCGAA | 57626 |
rs17086085 | snp | A/G | 0.251014 | 0.249998 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980837 | ATACATCTCTGCCAT[A/G]TCAAACATTTTAGGA | 57626 |
rs17086090 | snp | C/T | 0.250732 | 0.249999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981004 | TCAGAATAGCTACCA[C/T]TAAATAAACAAGCAA | 57626 |
rs17086099 | snp | C/T | 0.250732 | 0.249999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981364 | AGAGAGTAACGAAAA[C/T]GGCAAAATAAATTTG | 57626 |
rs17086108 | snp | A/G | 0.250732 | 0.249999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981559 | TAACTATTTGTTTGA[A/G]CCCAGTAAACTTAGT | 57626 |
rs17086184 | snp | A/G | 0.128288 | 0.218372 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009796 | CTAGATTTATTGCCA[A/G]TTTGGATCCATAGTA | 57626 |
rs17086297 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062238 | CTATCTTGAGCTCAT[G/T]AGAAATTTTGAGATA | 57626 |
rs17086301 | snp | A/G | 0.0908922 | 0.192833 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064075 | CTTTAGTTAGAGGAC[A/G]GATTAATGGACACAA | 57626 |
rs17086304 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065173 | CTTCCTTCAGTGATT[A/C]TTTTGTGACTGTAGA | 57626 |
rs17086324 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066915 | CTATCTAGACATATT[C/T]GCTTATTCATAGAGT | 57626 |
rs17086326 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067742 | GAGACTTTCTAAGAG[C/T]TGCTGGAATCCAGAA | 57626 |
rs17086338 | snp | C/T | 0.077417 | 0.180873 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080046 | TTTGTGGATAGGTAC[C/T]AAGATGTGTTTTCTT | 57626 |
rs17086355 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093279 | CATCATAGTGGAGTG[G/T]ACTTTGTCTTTCTCC | 57626 |
rs17086366 | snp | C/T | 0.268995 | 0.249277 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104426 | TGACCTTTCCAGAAT[C/T]CTGAGATTGTGAGCA | 57626 |
rs17086370 | snp | A/G | 0.284733 | 0.247575 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105366 | AAAACTCCAAATTAC[A/G]TAAAAGTCTTTATAA | 57626 |
rs17727284 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769151 | TCATTGCACAGGGTT[G/T]TAAGTCAAGGAAGAC | 57626 |
rs17727926 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794867 | TCTCAGGAAAGGATA[A/C]AGACAAAAATATAAA | 57626 |
rs17727950 | snp | A/G | 0.392981 | 0.205076 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796721 | CTAAAAGTAATATCA[A/G]TAAAGTAAGATCTTA | 57626 |
rs17728004 | snp | A/T | 0.396182 | 0.202807 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797149 | TCTTGGCAGACATGA[A/T]TGATCAAAATAGACA | 57626 |
rs17728354 | snp | C/T | 0.396364 | 0.202676 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803381 | TCCACAATATTAACC[C/T]GGCTCTAGAGCCCAC | 57626 |
rs17734162 | snp | A/C | 0.0155029 | 0.0866667 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823061 | TCTGTGAAGACATAG[A/C]AGCCTCACCTCCGAT | 57626 |
rs17736182 | snp | A/C | 0.300169 | 0.244914 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857470 | TGACTAGCAAAAGGT[A/C]TGCCACAGAGTTGAC | 57626 |
rs17739613 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960060 | CCAAAAAATGTCTAA[A/G]TATTTTCCTCACATT | 57626 |
rs17742723 | snp | A/T | 0.111224 | 0.207945 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061278 | ATGTAGCTACACAGG[A/T]CTCACAATTAAAAGC | 57626 |
rs17743943 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094610 | GTAAACCACCACATT[A/G]CATACCTCCAAGTAA | 57626 |
rs17787264 | snp | C/T | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705498 | ATATGGAATAACCAA[C/T]TTAGTCCACTTACAG | 57626 |
rs17794771 | snp | A/G | 0.383632 | 0.211288 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771621 | TAAGAAGTAGTTATG[A/G]AAGTCTAACTTGAGA | 57626 |
rs17796136 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822659 | ATTACAAGTTATGTG[C/T]AACAAAAATACCTCA | 57626 |
rs17798262 | snp | A/G | 0.349013 | 0.229557 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858309 | CTTGAGAGAGGAGAG[A/G]TAGACCTAATAAGGA | 57626 |
rs17810777 | snp | A/G | 0.174932 | 0.238463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913503 | TGAAAGATGCTGCCT[A/G]AACCTGCTGCTTCCT | 57626 |
rs17813693 | snp | G/T | 0.316 | 0.241131 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007876 | CTAAGACATATTTTT[G/T]GCACTGCCTGAGTCC | 57626 |
rs17813717 | snp | C/T | 0.316 | 0.241131 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007946 | AAGCAGCCCCAAAAA[C/T]GCCACATTAGCTTAC | 57626 |
rs17822424 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097362 | TAATTTGTCTTCATG[A/T]GCAAGGTAGGAGAAA | 57626 |
rs28360776 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69819284 | TCAGGGGTTTAATCC[C/T]TAAAGTTATGTAATT | 57626 |
rs28366674 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69922190 | GGTCTCAAGGGATTC[C/T]CCTGCCTTGGCCTGC | 57626 |
rs28402140 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69975514 | AAAAACTTAAAAAAA[C/T]GTGAATCCTTATTTC | 57626 |
rs28489714 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69714735 | AGTAGCTGAGGCCCC[A/G]GGGATGTGCCACCAC | 57626 |
rs28490086 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69746105 | GCATTTTTAAATTTT[C/T]TATTTGTTTCATCAA | 57626 |
rs28521617 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69822031 | GGTGAAACCCCATCT[C/G]TACCAAAAATTAAAA | 57626 |
rs28544458 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70007733 | TACAAATTAAATTTT[A/T]AAAAATCATAAACCA | 57626 |
rs28576389 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001536 | TGATTTATTTCAGGT[A/T]TGCAAGAACATTTAA | 57626 |
rs28644221 | snp | A/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69775703 | TAAGGGTTTTTTTTT[A/G/T]TTTTTGATACAGTGT | 57626 |
rs28666938 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086590 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 57626 |
rs28690017 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69935805 | ACACTTGTAGTCTTG[G/T]TGAATGAGTAAATTA | 57626 |
rs28720786 | snp | A/T | 0.407363 | 0.19426 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804298 | ATGTAGACAAATATA[A/T]TTTTTTTGTGGGGGG | 57626 |
rs28726207 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70007694 | ATAGAAAATAATTTC[A/C]ACTTTCCTAGTACTG | 57626 |
rs28737370 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824571 | TTACTATTAATTAAT[A/T]AAAAAGAAGATAGGG | 57626 |
rs28758436 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69756677 | AAGAATCAAACTATC[G/T]GGGATGATTCAACAG | 57626 |
rs28760376 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69898299 | CATGGACCTCAGGAC[G/T]GGGTTTTAAAACCAA | 57626 |
rs33926726 | in-del | -/AAGA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70014561 | CTATTGAAAATGATA[-/AAGA]AGTGCAAAATAAAGT | 57626 |
rs33948512 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69969942 | TCGATTAAACTTTTT[-/G]AAGTTCCACTTCAAT | 57626 |
rs33971927 | in-del | -/A/AT/ATAT/T | 0.499872 | 0.0079862 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075760 | CACACATACACACAC[-/A/AT/ATAT/T]TATATATATATATAC | 57626 |
rs34005132 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69732769 | TTTTTCTAAGACACG[-/C]CCATCGGCTTCATTG | 57626 |
rs34007505 | in-del | -/A | 0.499325 | 0.0183582 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014995 | ATTAAGCAAACATGC[-/A]AAAAATTATTAAAAA | 57626 |
rs34007520 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69972034 | AGATATTTTAAACTA[-/T]TCAAACTGAGTGAGA | 57626 |
rs34008084 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039832 | TTTAGTACAGATGGG[-/T]TTTTCACCATATGGG | 57626 |
rs34013855 | in-del | -/A | | | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970361 | AATTTATGAACTTCC[-/A]AGAGTCAAAATTATG | 57626 |
rs34017273 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69981942 | TATTAAAATAATAAC[-/T]TTTTTTTCAGAAATA | 57626 |
rs34046439 | in-del | -/A | 0.461481 | 0.133325 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809016 | AGAAAAAAATAAAGT[-/A]AAAAGAATTTCAAAA | 57626 |
rs34046996 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69769139 | AAAGAATCACTGTCA[-/T]TGCACAGGGTTGTAA | 57626 |
rs34051781 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70055000 | ATATAAATTGGGGTT[-/A]AAAAGTTTATTCAAA | 57626 |
rs34056229 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69857051 | ACAATAGTAAATTCC[-/T]GAACCTGATAGAACA | 57626 |
rs34058717 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69784913 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 57626 |
rs34060557 | in-del | -/A | 0.464841 | 0.127841 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088389 | AATATATACAAATAT[-/A]AAAAAAAAGGCCAGG | 57626 |
rs34069392 | in-del | -/AT | 0.375 | 0.216506 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866946 | GACCTAAATTATCAC[-/AT]GTTTAATCATTACAC | 57626 |
rs34074889 | in-del | -/A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939340 | ACATATACATACATA[-/A/T]ATATATATATATATA | 57626 |
rs34105052 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69818917 | ATTGCTTTTCTTCAG[-/A]AAAAAGTCATACAGT | 57626 |
rs34106617 | in-del | -/T | 0.480461 | 0.0968913 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969057 | AAACTTTTTAGGAGA[-/T]TTTTTTTCATTTATT | 57626 |
rs34112433 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69994605 | TGTACTAATGTATAT[-/G]GGAAAAGTACATTGG | 57626 |
rs34129651 | in-del | -/A | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976260 | GTGATTTTTATTATG[-/A]AAAAAATATAAAACC | 57626 |
rs34158219 | in-del | -/TA | 0.375 | 0.216506 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833800 | ATACTTGTTGTGTTC[-/TA]TATATATATATACAC | 57626 |
rs34163072 | in-del | -/AT | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813503 | CACACACACACACAC[-/AT]ATATATATATATATA | 57626 |
rs34168639 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69737302 | GGCACTGGACACAGG[-/T]AGTATTTGCATACTT | 57626 |
rs34183465 | in-del | -/TAA | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982439 | GACTCCATCTCCAAA[-/TAA]TAATAATAATAATAA | 57626 |
rs34190830 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69909428 | AGAGGCTAAAACTGC[-/A]AAATATTTGAAGCAA | 57626 |
rs34192638 | in-del | -/AAAA | 0.433003 | 0.170323 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056998 | TGTAACAAAAATATC[-/AAAA]AAAAAATTGAAAAGT | 57626 |
rs34204892 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69906842 | AGTATAACTCTCACT[-/G]GGAATAGAAAAAATA | 57626 |
rs34214995 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69848632 | CATGGCTGTCACTTC[-/A]AAAATGAAAACACAA | 57626 |
rs34228544 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69955945 | ATTTGATATATATTT[-/TA]ATATATATATTTGAT | 57626 |
rs34228703 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69816267 | AAATTTTTTTTCTTT[-/C]TTTTTTTTTTTTGGA | 57626 |
rs34233799 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69802925 | TTGATTATTTTCTAT[-/A]AAAAGTATTTATAAG | 57626 |
rs34250203 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69886488 | CCACATTAATTATTG[G/T]TAATAATATATATAT | 57626 |
rs34276563 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936120 | CTTGAACTAGAAACA[-/G]GGGAGAGATTATTCA | 57626 |
rs34280840 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70033766 | TGGAATTACAGGCAC[-/T]GCACCACCACAGCCG | 57626 |
rs34281402 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70064345 | ATGTAAGTGTGAATA[-/G]GGGAAATCAATGAAG | 57626 |
rs34283818 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69747465 | GGTATTATGATGAAG[-/A]ATGATAAGAATTAAT | 57626 |
rs34284496 | in-del | -/C | | | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701367 | TGGTCATGAAACTAT[-/C]CCATGTCACAAATAT | 57626 |
rs34287949 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69735220 | AGCTACAGACAATAA[-/G]AATACTGCCTTTAAC | 57626 |
rs34315693 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69765932 | CCTAAGTTATTGCTA[-/T]TTTTGGATTTTACTC | 57626 |
rs34317213 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026169 | CTAGGTAAATGGACA[-/T]TTTGATAGCACCAAA | 57626 |
rs34317558 | in-del | -/A | 0.0905309 | 0.192535 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920686 | TACCTTTTCATACTT[-/A]AAATGCCACAGAACA | 57626 |
rs34321855 | in-del | -/A | 0.420255 | 0.183066 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764535 | ATTTCTACTAAAAAA[-/A]TGGCACAAAGAAAAA | 57626 |
rs34324121 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69820691 | GGGATGCCTGTTCAA[-/G]GGGACATTCAGGCCG | 57626 |
rs34340593 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70077259 | GTGGTACACCCATAC[-/A]AAAAGTGTAATTCAA | 57626 |
rs34349675 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69723147 | GAATTTGAGAGTAAA[-/C]ACAGTGGTTATCAAA | 57626 |
rs34356266 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70053094 | AAATTAGATTGAAGG[-/A]AAAAATGAAAAAGCG | 57626 |
rs34359873 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70072820 | AAAAAACTTTTATTT[-/A]AAAAAAAACTACACC | 57626 |
rs34373404 | in-del | -/A/AA | 0.254105 | 0.249966 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819617 | ACAAGGAGGTAATGC[-/A/AA]AAAAAAAAAAAAATG | 57626 |
rs34387351 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69732737 | GCTCTGTAGCACCAG[-/A]ACACACCTAGTTTGC | 57626 |
rs34395344 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095829 | TCCCTTCTCCCTCCA[-/C]CCCCCCCCACCACAC | 57626 |
rs34408474 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69861785 | AACCCCGTCTCTACT[-/A]AAAAAAAAAAAAAAA | 57626 |
rs34418967 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69941178 | CTTTTCATCAGCACA[-/G]GGGAACATTCTCCAA | 57626 |
rs34421047 | in-del | -/A | 0.419296 | 0.183954 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074744 | AAGAAAAAAAAAAAA[-/A]TTATGCTGTTGATCA | 57626 |
rs34471023 | snp | A/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997215 | TACAGAGTGAGACTC[A/T]GTCTCAAAAATAAAT | 57626 |
rs34481284 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69743785 | GTGAGATTTTGTCTC[-/A]AAAAAAAACACCAAA | 57626 |
rs34483205 | in-del | -/T | 0.16028 | 0.233346 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712261 | GTCTTTCACACCTCA[-/T]TTTTTTTTTTTTAAG | 57626 |
rs34484817 | snp | C/T | 0.435119 | 0.16802 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858987 | TCACCTATTCATATA[C/T]GTGTCCATCCAAACT | 57626 |
rs34489516 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69840910 | GTGTCAAATATATAG[-/T]TTCTTGTATCTGAGT | 57626 |
rs34493251 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69765769 | GAATTGAAGCAACCA[-/C]CCCAGGCAATGCTAC | 57626 |
rs34500085 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69905682 | ATGTATTATTTAATT[C/G]TAATAATTCAGTGAA | 57626 |
rs34507352 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69937788 | TGAAATTTCCAAAGG[-/G]AAAGATGACAAATAA | 57626 |
rs34513199 | snp | A/G | 0.431916 | 0.171483 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027537 | TCATACAGCAAAGGG[A/G]GAGAAAACTATAACA | 57626 |
rs34537024 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884397 | TTAACAAATTAAGTG[-/T]TTCTGAGATGTTTTG | 57626 |
rs34547829 | snp | A/C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69803072 | TAACCAAGAGAATTC[A/C/G]TGATATGTATATTAT | 57626 |
rs34550775 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69818664 | TTTCAGAAGAAAATT[-/A]CTTTGTGTGTGAAAT | 57626 |
rs34582287 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69972534 | TCTGTTGATACATTT[-/C]CAGAAAAAAGCCACC | 57626 |
rs34586533 | in-del | -/G | | | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110288 | CCTTTCTATATTTGT[-/G]CAATCTTAATACAAT | 57626 |
rs34595062 | snp | A/C | 0.227959 | 0.249026 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855717 | GTTTCCTGAGGCCTC[A/C]CCAGCCATGCCGAAC | 57626 |
rs34603273 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70104239 | CAGTGAACTATTATA[-/G]GGAAAAGTATTGTTT | 57626 |
rs34612932 | in-del | -/T | 0.375 | 0.216506 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859259 | TCATCCATTTTGCAC[-/T]TTTTTTTTTTTTTTC | 57626 |
rs34615852 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837646 | ATATATATATATGTG[-/TA]TATATATATATGTGT | 57626 |
rs34618345 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69866377 | AGCTAATTTTAATAG[-/C]AAAAAGCTAAAACAC | 57626 |
rs34619622 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69722634 | GCAAAAGCTATTGCC[-/A]AAAAAAATTAAAAAT | 57626 |
rs34624578 | in-del | -/TTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69881750 | TCTTAACTCCAATTA[-/TTA]CATATTCCATAATTC | 57626 |
rs34628378 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69749492 | CTTTTTGCATATACT[-/C]CCCCTTGAGAATTCT | 57626 |
rs34634895 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69814844 | GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 57626 |
rs34654235 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69872651 | CCTTTTGAGAATACT[-/C]CCCAGTGGCCTCCTT | 57626 |
rs34662690 | snp | C/T | 0.163236 | 0.234461 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853656 | TTAAAGTGGTATTCA[C/T]CAGTGAATGTGATAA | 57626 |
rs34668618 | in-del | -/AC | 0.506728 | 0.0511269 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954800 | AGTACTAAATGTTTT[-/AC]ACACACACACACACA | 57626 |
rs34673095 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70056434 | GGAAAGACCATCCAG[-/T]AAAGAAAATCAACAA | 57626 |
rs34679999 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70028993 | TAAAAAAAAAAAAAA[-/AA]ATCACTATTCCTGAT | 57626 |
rs34687973 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70002420 | AAAATAGGAAGGGAG[-/A]AAAAAAATTTTTTTA | 57626 |
rs34694868 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69878904 | GTACATACACACCAT[-/G]GGAATACTATGCAGC | 57626 |
rs34705159 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69957475 | TGCATTCGCTATATT[-/C]CCTTGATTTACAACG | 57626 |
rs34705498 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69835386 | AGGAACAGTGAGGTG[-/A]AAACCAGAGAGAGAG | 57626 |
rs34709071 | in-del | -/ACTT | 0.354235 | 0.227234 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709890 | TTTCTAGTACAAATA[-/ACTT]TAAAGTGAATAATTT | 57626 |
rs34720128 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69997361 | GTTGAATGCACAATG[-/C]CAGTATTTGGTAACT | 57626 |
rs34733572 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100446 | GACAATTGTATCTGC[-/A]AAAAGTTTTATTTCT | 57626 |
rs34765282 | in-del | -/A | 0.211516 | 0.24702 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855925 | TATGTTATAACATAT[-/A]TAATATGCATGTTTT | 57626 |
rs34767951 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70013358 | ACATGGCTACTCTAC[-/T]TGACTGCAGAGGAGT | 57626 |
rs34771072 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060028 | AAACCATATCACTCT[-/A]CCATGAGATAAAGGA | 57626 |
rs34782280 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947868 | TAAAAGTTAACTTTT[-/A]AAAAAGCATGAAAAC | 57626 |
rs34785152 | snp | C/T | 0.304688 | 0.243945 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823119 | GCCACAGATGAATAA[C/T]ATATGTCATAATATT | 57626 |
rs34793863 | in-del | -/AC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69862276 | AATTATACTGTTTTT[-/AC]ACACACACACACAGG | 57626 |
rs34795955 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69841520 | TGAAAGATCTCTACA[-/G]GGGAAAATTACAAAA | 57626 |
rs34815578 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70085205 | AAAAGCTAAACAAAG[-/A]AGAGAAACAGAAAGA | 57626 |
rs34820595 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69784846 | GGACCTAATAGACAT[C/T]TACAGAACTCTCCAC | 57626 |
rs34821362 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69925867 | TGTGAGTTATGGTTT[-/G]TTACTTTGCAATAGA | 57626 |
rs34821978 | in-del | -/TT/TTT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076387 | CTTTTTTTTTTTTTT[-/TT/TTT]AATGGTTTTGGATCA | 57626 |
rs34871954 | in-del | -/T | 0.375 | 0.216506 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732657 | TGTTTGTTTGTTTGC[-/T]TTTTTTTTTTTCCTG | 57626 |
rs34892755 | in-del | -/T | 0.470908 | 0.117046 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061341 | CAGTCCTGAATTCCA[-/T]TTTTTTTTTTTCTGA | 57626 |
rs34910448 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69967886 | GCAAGATGCTGAATC[-/A]AAAAAAAAAAAAAAG | 57626 |
rs34918434 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69794979 | AAGGCTGAAACTTTA[-/C]CATTGGAAGAGCAGC | 57626 |
rs34926839 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69798094 | AGCTCCCAAATGTTT[-/AT]ATAAGATAATATAAG | 57626 |
rs34928597 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855867 | GTTATATAATATATT[A/G]TATATTATATATGTT | 57626 |
rs34929194 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70052893 | ATTTATTATTTTATT[-/C]CCTTACATTGATATC | 57626 |
rs34929824 | snp | A/T | 0.471292 | 0.116318 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862192 | AGCAAATTACACATA[A/T]ATTATAATTAGAAGA | 57626 |
rs34954645 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69802814 | AGTCTTGCCGATGCT[-/C]CCCGGCTGAATAAAC | 57626 |
rs34958171 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69818586 | AACTTAGTTCTTCCC[-/T]TGGGATGCTTGGGGA | 57626 |
rs34981012 | multinucleotide-polymorphism | CC/TG | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017424 | CTGGTCCAGCTGCAA[CC/TG]TCAAAAAGAGCCAAC | 57626 |
rs34988139 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70004947 | CTATTACCTATCTAC[-/A]AAATATTACAAGTAA | 57626 |
rs34989454 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075480 | CTTATTTGCTCAAAA[A/G]CAACTGAAGCAAATA | 57626 |
rs35004578 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837616 | TACATCTCTCTCTCT[-/A]TATATATGTGTGTGT | 57626 |
rs35024026 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69832214 | TCTATAAACTCACGC[-/A]AAAAGCTCCTAGATC | 57626 |
rs35032606 | snp | A/T | 0.212122 | 0.247114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855626 | GGGGCTCTCCCTGCT[A/T]CACTCAGCAATTTTC | 57626 |
rs35055083 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70070434 | AGAAACCATGCAGGC[-/A]AAAAGAGAGTGGAGT | 57626 |
rs35057277 | in-del | -/AC/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70045576 | ACACACACACACACA[-/AC/CA]AGGAATCCTCTTTGG | 57626 |
rs35060900 | snp | G/T | 0.456568 | 0.140818 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798099 | CCCAAATGTTTATAA[G/T]ATAATATAAGCTAAC | 57626 |
rs35062740 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69918869 | ATCTTTATAAAACAC[-/G]GGGTTGTGTAATTCT | 57626 |
rs35070272 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69773208 | ATATCTGCTATACAC[-/T]TTAAGGGAATATAAT | 57626 |
rs35073906 | in-del | -/G | | | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106768 | TAGATTCAAACCACA[-/G]GGGACCTTAGATAAT | 57626 |
rs35140817 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69801719 | ACAACATAGGATATA[-/T]TTTATGTCCAATTTT | 57626 |
rs35153573 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69809568 | GGGAATTTTAGACAT[-/G]GGAAATGAAAGGATT | 57626 |
rs35158913 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100490 | TATGACAAACTTGTA[-/T]TCAAATAAAAAGTTT | 57626 |
rs35168835 | in-del | -/TTTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961829 | GATTTCTATTATGTT[-/TTTG]TTATTTGCCTGTTCT | 57626 |
rs35176135 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69957502 | ACGAGGATAGCACAT[-/C]CCAGATAAATCCATT | 57626 |
rs35184766 | in-del | -/T/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039056 | TATATCCTTTGCACA[-/T/TT]TTTTTTTTTTTTTTT | 57626 |
rs35190121 | in-del | -/A | 0.499809 | 0.00978247 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922457 | TAGGTCCGAGTTTAT[-/A]AAAAAGACTGTTTGC | 57626 |
rs35203493 | snp | C/T | 0.160938 | 0.233598 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837967 | TTATAAAATAAATCT[C/T]ATTTCTTTAGGCTTC | 57626 |
rs35225144 | in-del | -/A | 0.475613 | 0.107697 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960294 | TAGCAGAAATGCTGT[-/A]AAAAATAAAACTCCT | 57626 |
rs35231947 | snp | G/T | 0.212122 | 0.247114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855823 | CTAATAATATATATA[G/T]AAAATATTATATATA | 57626 |
rs35233942 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70030905 | ATAAAAAATGATAAA[-/G]GGGGATATCACCACC | 57626 |
rs35239507 | in-del | -/TA | 0.45384 | 0.144739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997682 | TTACTTATATATATA[-/TA]ATATAAATACATTGA | 57626 |
rs35249010 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69992924 | GAGGGAAAAAAAAAA[-/A]CATGTACCTTTCTTA | 57626 |
rs35264823 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70064661 | GTTGTAGTGCCTAAC[A/T]CGGTATCTGGTACAA | 57626 |
rs35265233 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69757118 | CCAAGCGATATGATC[C/T]TAAATCTTTTAGAAA | 57626 |
rs35265589 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69763620 | TAAATGATAGTAATT[-/G]GGTAGTAGCACTAAA | 57626 |
rs35287941 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69772380 | TCATTTTTGTTGGGG[-/A]AAAAATAAATCAAGC | 57626 |
rs35293449 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026511 | TGTAATGTATTTGGA[-/T]TTCTTATCCTAAAGC | 57626 |
rs35324869 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901486 | TGATATGCTTGGGTG[-/C]ACAATGATGACTCTG | 57626 |
rs35326746 | in-del | -/T | 0.139564 | 0.224285 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009958 | TATAATAAAGTCACA[-/T]TTTTAAGAGTAACCA | 57626 |
rs35332261 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69797827 | AGCGAGACTCCATCT[-/AA]AAAAAAAAAAAAAAA | 57626 |
rs35335979 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026343 | TATTAGTTCAACTCT[-/A]AAAACAGTACTACAT | 57626 |
rs35346749 | in-del | -/A | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822197 | GGGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 57626 |
rs35370725 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70028233 | TGTTAAGAATTATAA[-/T]TTTGATTAATATGGC | 57626 |
rs35388987 | in-del | -/CTT | 0.139903 | 0.224452 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009159 | TGTAAGTCACGACTC[-/CTT]CTATTAATAAGTCTT | 57626 |
rs35396811 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69957652 | AAACTGATATACAAT[-/G]TTTATAAGTACTGAT | 57626 |
rs35407264 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69772363 | AACAGCAAATTTTTT[-/C]CTCATTTTTGTTGGG | 57626 |
rs35413160 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70014960 | AACATATGGTTTATT[-/A]AAAATTAAGCAAAAC | 57626 |
rs35414727 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075540 | TTATATATTGCATAC[-/AT]ATATATATATACCTG | 57626 |
rs35421658 | snp | C/T | 0.434976 | 0.168179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861571 | GTATATATATACACA[C/T]GCACATATATGCAAT | 57626 |
rs35454437 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69902035 | GAACTCCCAACCTCA[-/G]GTGATCTGCCCACCT | 57626 |
rs35457419 | snp | A/G | 0.284995 | 0.247539 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827601 | TGGGTGTGGTGGTGC[A/G]TGGCTGTAATCCCAG | 57626 |
rs35458833 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69707075 | CATGACAGGCTATGC[-/A]AAAGCCCTTTCCTGT | 57626 |
rs35480286 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69872636 | TCTTGGGGAGACACT[-/C]CCTTTTGAGAATACT | 57626 |
rs35498984 | snp | A/C | | | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700427 | GTGAATACAGAAGAA[A/C]CAATAATTAAAATTA | 57626 |
rs35502395 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69987561 | AGGAAGGGAGGGTGG[-/C]AGTAAAGGGAATGAG | 57626 |
rs35503849 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70074819 | AAAACATAAGAACTC[-/A]AAAAAATAAACAAAT | 57626 |
rs35506043 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69834022 | TCTCATTTATAAGTG[C/T]GAGCTAAGCTATGAG | 57626 |
rs35507636 | multinucleotide-polymorphism | CG/TA | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855839 | AAAATATTATATATA[CG/TA]GTATTATATATGTTA | 57626 |
rs35521937 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69959557 | ATTAAAAAAAAAAAA[-/A]CATGGAATTGTAATT | 57626 |
rs35527264 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70000928 | TTACAGAAAAAAAAA[-/A]CAAAAAATAGATGCC | 57626 |
rs35538242 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69872607 | TCACCCCATAAAACC[-/T]CTCCCGTCACTTTCT | 57626 |
rs35548126 | in-del | -/A/AA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073557 | TAATAAAAAAAAAAA[-/A/AA]TGTAGGCAATAGCCC | 57626 |
rs35553547 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70101037 | ACATGTAGACATGAG[-/C]AAGCATAATACCTGA | 57626 |
rs35572998 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69747300 | ATAATGTAATATAAT[-/G]CTATTGTATTGATTG | 57626 |
rs35601149 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69945994 | ATACTTCATAATAAT[-/A]AAAATAAAATAATTA | 57626 |
rs35604564 | snp | A/G | 0.396727 | 0.202413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073814 | AAAATTGAAATGCAG[A/G]AGAGCAAACATAATT | 57626 |
rs35622532 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69893704 | TTAATATATTTTGTA[-/C]CTAAGATGCAGGAAA | 57626 |
rs35629466 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69905689 | TTTAATTCTAATAAT[-/C]TCAGTGAACAATAAT | 57626 |
rs35634358 | in-del | -/CAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69790254 | CAAAAAAATATTAAA[-/CAA]CTCTGGAAACTAAAA | 57626 |
rs35635135 | in-del | -/TAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69851105 | AAAACATACATATAT[-/TAC]ACTTTTATTTTTTAT | 57626 |
rs35637769 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70055518 | CACAGACAAATACAA[-/G]AATATTGTAACACTA | 57626 |
rs35653476 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69765162 | TTGCCATGTTGGCCA[A/G]AATGGTCTTGAACTC | 57626 |
rs35664442 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996536 | TGTGAAGCTGTCAAC[-/T]TTCCCATAACACTTT | 57626 |
rs35664789 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69765268 | TCTTTGCATGTTTTA[-/T]TAGTGATGGTAATCT | 57626 |
rs35671461 | in-del | -/CTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69709662 | TAAAAAATAAAGTCA[-/CTT]TTATTTTTGTTTGTT | 57626 |
rs35688050 | in-del | -/TT | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979437 | TTCACAACAGAACAC[-/TT]ATAATTTTTAAGATA | 57626 |
rs35692819 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69939098 | GTAAAAATAGGTAGC[-/G]ATTGATACAGGGCGT | 57626 |
rs35694317 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022072 | CCAAAGTCACTTTGA[-/T]TTTTCTCCTTTTTTC | 57626 |
rs35695560 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69720507 | AACAGGGATAGACAG[-/A]AATATACAAAGTAAA | 57626 |
rs35720226 | snp | A/G | 0.089084 | 0.191327 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833749 | TAAAGAAATAATGGT[A/G]TATATATATATATAT | 57626 |
rs35732802 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69890864 | AGATATTTTTTGACT[-/G]CTATATTGCTTCTTT | 57626 |
rs35738245 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69774166 | CCTAATAATCAGGCC[-/T]TTTCCAGTAAAGGAG | 57626 |
rs35739150 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69814450 | AAGAAACTATCAACA[-/G]GAATAAACAGACAAC | 57626 |
rs35739402 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70033780 | CGCACCACCACAGCC[-/G]GGCTAATTTTTTTAT | 57626 |
rs35739445 | in-del | -/AC | 0.375 | 0.216506 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833857 | TACACACACATATAT[-/AC]ACACACACACACACA | 57626 |
rs35744000 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70073155 | CAGACTTGGAACCAA[-/C]CCCAAATGTCCATCA | 57626 |
rs35761520 | in-del | -/TTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69903630 | CCCTTGTTCACATTC[-/TTT]TTTTTTTTTTTTTTT | 57626 |
rs35773928 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69792287 | GAGCTTTCTCCAAAG[-/C]AAGGTATACAAAAAA | 57626 |
rs35778278 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69972468 | CTTCATTTAAGTTTT[-/C]CATTTGATCATGAAC | 57626 |
rs35780382 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69708680 | TATTTTATATTTTGA[-/C]GTAGCAAAACCCTGA | 57626 |
rs35780612 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69735554 | TAATTATTAATGTAT[-/G]AAATAGATATAAATA | 57626 |
rs35781936 | snp | A/G | 0.01242 | 0.0778188 | intron-variant, missense, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975774 | CCAAATCACTTTGAG[A/G]TGTCATTGAATGGCC | 57626 |
rs35788056 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855648 | GCAATTTTCCTTCCT[A/G]CCGCCTCGTAAAGAA | 57626 |
rs35789510 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69990455 | GACATGCATAATCTC[-/A]AAATAAAGGGATGAA | 57626 |
rs35792091 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69733723 | ACATGGAGCATTCAG[-/C]AATTTAAAAATCTGT | 57626 |
rs35799069 | in-del | -/T | 0.4628 | 0.13121 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754004 | ACCATGCCTGGCTAA[-/T]TTTTTTTTTTGTTTT | 57626 |
rs35807908 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70062900 | TGCCTTTTCAGTCAA[-/T]TTTTTTTCATGTTCA | 57626 |
rs35815396 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70046034 | TCTACTCTCTTTCTC[-/T]TAAAATGCGAAGTGG | 57626 |
rs35817376 | snp | C/T | 0.127254 | 0.217792 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789622 | AACAAATGACCATTT[C/T]TTTTCCTCTACTGTC | 57626 |
rs35828287 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69763908 | TGTTGTAACCCTTAC[-/A]AAAAAGTAACCTGAA | 57626 |
rs35833390 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70074614 | ATGATAAACATGTTT[-/G]CCTTGACACAGAATT | 57626 |
rs35835793 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69753252 | AAATAAAAAGGCTGT[-/A]AAAAAGGCTGAAAGA | 57626 |
rs35845179 | in-del | -/TTAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789329 | GTCTTATTTAATAAA[-/TTAA]TTAAAAATATAAAAA | 57626 |
rs35849145 | in-del | -/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70045585 | ACACAACACACACAC[-/CA]ACACACACAAGGAAT | 57626 |
rs35850592 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837615 | ATACATCTCTCTCTC[-/T]ATATATATGTGTGTG | 57626 |
rs35853463 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69880815 | TTGTGCACAACATAA[-/T]TTCCAAACTCCCCAC | 57626 |
rs35877179 | in-del | -/A/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855865 | TGTTATATAATATAT[-/A/AT]TATATATTATATATG | 57626 |
rs35878955 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69873706 | CATGGCACATGTATA[-/C]CCTATGTAACAAACC | 57626 |
rs35894102 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006503 | TTTTTTTTTTTTTTT[-/T]CAAAGAGTTTGAGAA | 57626 |
rs35894775 | snp | A/G | 0.435837 | 0.167226 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858982 | TTGATTCACCTATTC[A/G]TATACGTGTCCATCC | 57626 |
rs35900082 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70041599 | GTAAGGTATAACTGC[-/T]TTCCCATCTGGCATC | 57626 |
rs35900149 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833748 | ATAAAGAAATAATGG[-/T]ATATATATATATATA | 57626 |
rs35916434 | in-del | -/T | 0.493432 | 0.0569306 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718413 | GATCAATATTCTAGG[-/T]TTTTTTTTCATTTTG | 57626 |
rs35944084 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69916960 | AGAGTGTGTAGGCTA[-/T]TTTTTGAGTAAAGTA | 57626 |
rs35944932 | in-del | -/T | 0.452842 | 0.146134 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936421 | AGGTGAAACCTCGTC[-/T]CTACTAAAAATACAA | 57626 |
rs35958207 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69817313 | TCCTGATTGTATGGC[-/A]AAAAAAGAAGTCATA | 57626 |
rs35987280 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69866767 | CAGGGACAAAGCATT[-/G]GGGAAATGCTTATCT | 57626 |
rs36002995 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69938791 | TGCATATCTTCTTCC[-/T]TTTATTTCTATATTT | 57626 |
rs36006378 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961619 | AACTCTTCCCCTAAC[-/T]TTTTCGTAATAGAGC | 57626 |
rs36012094 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70078743 | ATTCAGTCCAGTGGC[-/A]AAAATGTGGTTTTTA | 57626 |
rs36016680 | in-del | -/AGC | 0.493201 | 0.0579089 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717759 | AGTTGTCAGTCTATT[-/AGC]AGCATTTTTAAAATA | 57626 |
rs36029415 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69865515 | TTAATTTGTGTTTTT[-/A]AAAAAATTTACTGAA | 57626 |
rs36036500 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69801062 | TTCGGGTGATGACTA[-/C]CCTAAAGCCCTCGAT | 57626 |
rs36036605 | in-del | -/ACTC | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001212 | TATAAAACAGGAAAT[-/ACTC]AGGAAATAGAAATAA | 57626 |
rs36043772 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781970 | TTTCTAAAACTTTTA[-/T]TCAATACTCAATTGC | 57626 |
rs36053652 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849016 | AAAATAAGTTAACCT[C/T]CCACCCTGTATGAAC | 57626 |
rs36059777 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69971713 | ATATATTCTACCTTG[-/C]CAGTTATTTGCAACT | 57626 |
rs36068601 | in-del | -/TATG/TG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837656 | ATGTGTATATATATA[-/TATG/TG]TGTGTGTGTGTGTGT | 57626 |
rs36080070 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69765457 | AGGTAAGATAATGAG[-/C]AGCTTGATTCAAACT | 57626 |
rs36080656 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038384 | ACAGGTTTTTATGTA[-/T]GACATGAGTATTCAG | 57626 |
rs36097461 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69784990 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 57626 |
rs36097609 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69818587 | CTTAGTTCTTCCCTT[-/G]GGGATGCTTGGGGAA | 57626 |
rs36120714 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70004269 | ACATTAGAAATTTAG[-/A]AAAAAGTAGGACCTC | 57626 |
rs36191901 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70073408 | ACTAGGGCCTGTTGT[-/G]GGGGTTCGGGGAGGG | 57626 |
rs41283964 | snp | C/T | 0.183568 | 0.241012 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700564 | CTTTATCCTTACATT[C/T]GATTTAAAATTTATT | 57626 |
rs41283966 | snp | A/C | 0.183568 | 0.241012 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700962 | CCAATAATTACACTG[A/C]ATCTTTGGCTCAGTG | 57626 |
rs41283968 | snp | A/C | 0.185155 | 0.241444 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700997 | AAAAAAGCAAAGCAA[A/C]ATGGTAAGCCTAGTG | 57626 |
rs41283970 | snp | C/T | 0.183886 | 0.241099 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701123 | AGGACAGTTTGTTTT[C/T]TGAATGCAAGATACA | 57626 |
rs41283972 | snp | A/G | 0.0955121 | 0.196554 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69839159 | TTTCTAGGTCAGCCA[A/G]TATCTGTGAATAATA | 57626 |
rs41283974 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940300 | AATATGTATCATAAC[A/C]CTACACAAAACATTA | 57626 |
rs41283976 | snp | A/T | 0.202546 | 0.245455 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961215 | GATACAGAATACAGA[A/T]TTTTTTTTAAAAAAG | 57626 |
rs41283978 | snp | A/C/G/T | 0.00141501 | 0.0265683 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107600 | GCAGGCAGCCTCCCC[A/C/G/T]CGCCGGGCCGCCGGT | 57626 |
rs41283980 | snp | A/C | 0.26078 | 0.249767 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108207 | CGCAGAGAGAAAGAG[A/C]CCCAAGTCTCGAGGA | 57626 |
rs41314442 | snp | G/T | 0.0759472 | 0.179459 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797069 | TCTTGTCATATTCAT[G/T]TTTTTTAAAAGAAAA | 57626 |
rs41417651 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933914 | TCTCGGTATCAGGAA[C/T]TCGACTTAATATTAT | 57626 |
rs55682423 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729159 | CCAAGCACCACACAT[C/T]GACGTTTATTCACTT | 57626 |
rs55704507 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012859 | AGTGAGGTGAGATCT[C/T]GCCCCTGCACTCCAG | 57626 |
rs55705420 | snp | A/G | 0.2462 | 0.249971 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038492 | GCCAAATTATTTTCC[A/G]GAGTGGTTGTGCTAT | 57626 |
rs55715266 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896890 | ATTGGCCAGGCTGGT[C/T]TCGACTCCTGACCTC | 57626 |
rs55719033 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727050 | AGGGAAAATTATTAA[C/T]TATGTGTCTCGGGAA | 57626 |
rs55723643 | snp | A/T | 0.178465 | 0.239547 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706457 | CTTGCAAAATCAAGG[A/T]AATCATGTTTCATTA | 57626 |
rs55732118 | in-del | -/TCAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69841212 | TATTGGAAGTCTTAG[-/TCAG]AACAATCAGGAAAGA | 57626 |
rs55748499 | snp | A/G | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841229 | AGAACAATCAGGAAA[A/G]AGAAAGAAATAAAAG | 57626 |
rs55749005 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833852 | ATATATACACACACA[C/T]ATATACACACACACA | 57626 |
rs55772300 | in-del | -/CTTG/CTTT/CTTTA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723848 | GTCAGAATTTTTTTT[-/CTTG/CTTT/CTTTA]TTTTTTTTTTCTGAG | 57626 |
rs55773148 | snp | A/G | 0.326506 | 0.238006 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948897 | TCACAACGTAAATCA[A/G]ATTTTATCTATCATC | 57626 |
rs55791676 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012523 | TTGGCAGTCTTTGAA[A/G]AGGGGGAGGGGGACT | 57626 |
rs55794521 | in-del | -/A | 0.488241 | 0.0757703 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968554 | ATTTAAAAAAAAAAA[-/A]GAAATTGAAGGTATT | 57626 |
rs55798326 | in-del | -/T | 0.252702 | 0.249985 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045841 | TAAGAGTATCTGCAT[-/T]ATTTCCCAGATTAAC | 57626 |
rs55800549 | snp | A/C | 0.0872718 | 0.189788 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736547 | ACTGCTGGGCCTCTA[A/C]CCAGAGGAAAGAAGT | 57626 |
rs55811703 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905182 | ATGGTTTTGCCTAGT[C/T]CAACAGAATGTAATG | 57626 |
rs55815844 | snp | C/T | 0.142609 | 0.225759 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714813 | TGTCCAGGATGGTCT[C/T]AAACCCCTGAGCTCA | 57626 |
rs55818434 | in-del | -/ATGAATTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69751925 | TAAGAGGATGTATTT[-/ATGAATTT]CTTTGCTTACACTCC | 57626 |
rs55857883 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833751 | AAGAAATAATGGTAT[A/G]TATATATATATATAT | 57626 |
rs55873061 | snp | C/T | 0.135825 | 0.222405 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833778 | ATATACATACATACA[C/T]ACATATATACTTGTT | 57626 |
rs55876065 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850433 | CTTTGGTCAACCTCA[C/T]ATCCAAACAGTCACC | 57626 |
rs55885952 | in-del | -/TT/TTT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038605 | TTTTTTTTTTTTTTT[-/TT/TTT]GAGATAGAGTCTCAT | 57626 |
rs55895432 | in-del | -/AA/AAAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69861808 | AAAAAAAAAAAAAAA[-/AA/AAAA]TACAAAATTAGCCAG | 57626 |
rs55902553 | in-del | -/A | 0.433382 | 0.169915 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863502 | AAAAACATAAGAAAT[-/A]AAAAAATTTTGCATT | 57626 |
rs55929819 | snp | A/C | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838814 | TGAATAAGAAGCAGA[A/C]AGCAGCTACAATTAA | 57626 |
rs55946233 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833844 | ATACATATATATATA[C/T]ACACACATATATACA | 57626 |
rs55958087 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833768 | ATATATATATATATA[C/T]ATACATACATACATA | 57626 |
rs55978749 | snp | A/G | 0.284733 | 0.247575 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998635 | CTCAATCAATAACTA[A/G]GACCTTAATTAGTTT | 57626 |
rs55988115 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69798102 | AATGTTTATAAGATA[-/TA]ATATAAGCTAACAGA | 57626 |
rs55988841 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69805702 | AAACAAAAAAAAAAA[-/A]CAAAACAACACTACA | 57626 |
rs55992117 | in-del | -/T | 0.142272 | 0.225598 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833445 | GCTATTGTCAAAAAA[-/T]AAAAAAAAATAGATG | 57626 |
rs55993203 | snp | A/G | 0.326506 | 0.238006 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948985 | AAATTGACATTTTTA[A/G]TAACTCATAGGTATT | 57626 |
rs56020679 | snp | A/G | 0.140919 | 0.224948 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834102 | GGGATGAAAGAGTGG[A/G]GGTTGAGGGACAAAA | 57626 |
rs56033252 | snp | C/T | 0.250732 | 0.249999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980577 | TCTGTACCTGGAACC[C/T]GCACAACACACTGAT | 57626 |
rs56044802 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69836862 | AAACTGCAAAAAAAA[-/AA]TGCAATAATTAGAAG | 57626 |
rs56046237 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020850 | TTGTATGTATTTTCT[A/C]TTTTTTACTTTATAT | 57626 |
rs56063161 | in-del | -/GAGGATCCTAGAAGAAGACTAGGCACCAGTAAAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69863391 | AGAATTAAAACAAAA[lengthTooLong]TATTAAGGTCTGAAA | 57626 |
rs56079035 | snp | A/G | 0.316 | 0.241131 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874366 | GTCTATATGCTATCA[A/G]TCTCCTATTTAATAC | 57626 |
rs56090652 | snp | C/T | 0.428484 | 0.175052 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032576 | TCTCATTCTTACTTA[C/T]GATGTTAGTTAAAAA | 57626 |
rs56103868 | snp | C/T | 0.141596 | 0.225274 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834134 | ACTACACATTGGGTA[C/T]GGTGTACACTGCTCA | 57626 |
rs56105976 | snp | C/T | 0.17461 | 0.238362 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822908 | TGGGTTTAAAATATA[C/T]ATGTGCAATTCAGTT | 57626 |
rs56125019 | snp | G/T | 0.265453 | 0.249522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987500 | ACAAAGTAAAAACAT[G/T]TAAATAACTTTAATC | 57626 |
rs56139044 | snp | A/C | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841337 | GACTCAACAAAAAAA[A/C]CAGTAGGTTTGATAA | 57626 |
rs56141962 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896118 | CCTGGAGGTCACTCA[A/G]CTTTTAGACACTTCT | 57626 |
rs56144213 | in-del | -/CTAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69980323 | TACTTTATGACCTAC[-/CTAC]TTAGTGCAAATCTGA | 57626 |
rs56151754 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70074380 | CAGTTATGACAGGTA[C/T]GGTTAGTTAGGATGC | 57626 |
rs56156636 | snp | C/G | 0.0905309 | 0.192535 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940539 | AAATAGAAAAATAAG[C/G]TTCAGAATATATGCC | 57626 |
rs56161743 | snp | A/G | 0.111576 | 0.20818 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930265 | AAAGAAAGTGCATCC[A/G]TTTACTATGATGGAT | 57626 |
rs56168989 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975505 | ACAACAACAAAAAAC[C/T]TAAAAAAATGTGAAT | 57626 |
rs56176574 | in-del | -/AACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69773051 | CACAGGCAGAAAACA[-/AACA]GAACAAGCAAAGGAA | 57626 |
rs56195401 | snp | C/T | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974065 | TGGTCTCGTGCTACC[C/T]GATCATGAGTTGCTG | 57626 |
rs56204941 | snp | C/T | 0.142272 | 0.225598 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833313 | CATGAATGGACAATT[C/T]TCAAAAGAACATAAA | 57626 |
rs56215515 | snp | C/T | 0.431473 | 0.171952 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027373 | TCCCTTTAGAGCCAG[C/T]TGAAAGTGAATGTTG | 57626 |
rs56217462 | snp | C/T | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802677 | CGGTGCATGCAGCCC[C/T]CCAGTCCCGTACCCC | 57626 |
rs56219140 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868951 | GTAAGGAGGGTACAC[A/T]GTTCAGTATGGCATC | 57626 |
rs56229908 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70074498 | CTGATTGATTATCGT[C/T]CACCCAAGAGATTCC | 57626 |
rs56235725 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70057491 | AAAAAAAAAAAAAAA[-/AA]GAGGCCGGGCGCGGT | 57626 |
rs56249509 | snp | C/G | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836607 | AGAAGGCAATTTTCT[C/G]TTACTCTAAGTGTTT | 57626 |
rs56254941 | snp | C/T | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836621 | TGTTACTCTAAGTGT[C/T]TGCCTAAAATAAAGT | 57626 |
rs56270453 | snp | A/C | 0.276534 | 0.248588 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872045 | CTGTTTTGTGTTGCT[A/C]TAAAGGACTACCTGA | 57626 |
rs56271435 | in-del | -/GT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730297 | TGTGTGTGTGTGTGT[-/GT]TTTCATTACAAAATA | 57626 |
rs56286102 | snp | A/G | 0.174932 | 0.238463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827083 | AATGTAATATGTTAC[A/G]TTAGATTTTGAAAAC | 57626 |
rs56293693 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872303 | ATAAACATGAGCAAT[C/T]GGCCTGTTTTACAGC | 57626 |
rs56310808 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69771613 | GCTTCTAGTAAGAAG[C/T]AGTTATGAAAGTCTA | 57626 |
rs56314159 | snp | C/T | 0.168135 | 0.236216 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833676 | GTGTTTATAGCAACA[C/T]AATTTGCAATTGCAA | 57626 |
rs56316232 | in-del | -/A | 0.433963 | 0.169285 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863483 | AATAGAGTGTATATG[-/A]AAAAAAAACATAAGA | 57626 |
rs56317930 | in-del | -/TC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69706881 | ATCTTCCCATCACAC[-/TC]ACACACACCAACACA | 57626 |
rs56327819 | snp | C/T | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833786 | ACATACATACATATA[C/T]ACTTGTTGTGTTCTA | 57626 |
rs56328038 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896913 | CTGACCTCATGATCC[A/G]CCCGCCTCAGCCTCC | 57626 |
rs56328604 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020620 | TGGAGAGCAGAAGCT[A/G]TACCTTTTATCTATG | 57626 |
rs56335733 | snp | C/T | 0.313326 | 0.241847 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949506 | CATCTTGATCACGTG[C/T]GGAGGTAGTGTATGT | 57626 |
rs56337520 | snp | A/G | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815311 | ATCAACCCAGTTGCC[A/G]ACCAATGGTTGATTG | 57626 |
rs56342320 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896875 | ACGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 57626 |
rs56347326 | in-del | -/T | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841159 | AATCTTTAAACTTTT[-/T]CCCCTTCAATATCAC | 57626 |
rs56347846 | snp | A/G | 0.142609 | 0.225759 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714679 | CTCACTGCAGCCTCA[A/G]CCTCCCCAGGCTCAA | 57626 |
rs56358950 | snp | C/T | 0.326506 | 0.238006 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949336 | TCCTTTTTTTAATGA[C/T]TTTGACAGTTTTGAG | 57626 |
rs56368243 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704056 | TCCCTGATGTCCATT[C/T]AATACTCAGTACTGT | 57626 |
rs56370134 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69736245 | CATGAATAGACAATT[C/T]TCAAAAGAACATATA | 57626 |
rs56371745 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70029529 | GTGAAGGAGAAATAA[A/T]ATACTTTACAGACAA | 57626 |
rs56376193 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896842 | TCACCTGGCTAATTT[C/T]TGTATTTTTTAATAG | 57626 |
rs56378647 | snp | C/G | 0.121717 | 0.214577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949117 | TAACATCTTACATTC[C/G]TATGATATACGTGTT | 57626 |
rs56390487 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841254 | TAAAAGGCCTCCAAA[C/T]TGGTAAAGAAGAAGT | 57626 |
rs56399751 | snp | C/T | 0.135825 | 0.222405 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833774 | ATATATATACATACA[C/T]ACATACATATATACT | 57626 |
rs56403924 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840695 | AACTTTATATATATA[A/T]ATATATGTATGTATG | 57626 |
rs56689981 | in-del | -/GT/GTGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69751149 | TGTGTGTGTGTGTGT[-/GT/GTGT]ATCTGTGTTGGGAGC | 57626 |
rs56730171 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69856612 | ATTCCAAACATTTTG[C/T]TCATCTGTCTGTTAA | 57626 |
rs56752911 | snp | A/C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69853680 | GTGATAATACAGTAA[A/C/G]TTTCTTATCAAGAGA | 57626 |
rs56790871 | in-del | -/CT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100189 | TATATATTCATATTT[-/CT]TCATTATGTGGCTCT | 57626 |
rs56852850 | snp | G/T | 0.132751 | 0.2208 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095805 | ACTGTATTTTTGTAT[G/T]GAATAACTGTCCCTT | 57626 |
rs56863220 | snp | C/T | 0.26518 | 0.249539 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987188 | TATCTCTGACTACAC[C/T]AAAAATACTAATTAA | 57626 |
rs56864128 | snp | A/T | 0.13446 | 0.221699 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730767 | AAATTATTTGTAGAG[A/T]TGGGGTCTCACTACG | 57626 |
rs56881253 | in-del | -/GCACAAAG | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983915 | TGATTTTTGACAAAG[-/GCACAAAG]ATCCCACAGTAAATG | 57626 |
rs56903484 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70088864 | AAAAAGAAAAAAAAA[-/A]CTTATCAGGGCTATT | 57626 |
rs56940937 | snp | A/G | 0.0869089 | 0.189476 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108258 | TCTTGGTGCACCTGC[A/G]CCCCTGTCCCTGGCC | 57626 |
rs56949730 | snp | A/G | 0.32627 | 0.238082 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943704 | TAGAGAAAATAATAC[A/G]AACACATTAAAATCT | 57626 |
rs56960573 | in-del | -/A | 0.29789 | 0.24537 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991677 | CAACCAAAAAAAAAA[-/A]GCCTGGGACCAGATG | 57626 |
rs56982017 | snp | G/T | 0.264358 | 0.249587 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987011 | TTAGATCATGAACAA[G/T]ATAAAATATATGTTT | 57626 |
rs57005049 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69809886 | AATGGAAAAAAAAAA[-/A]GCAGGATCACTATTC | 57626 |
rs57028630 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823836 | TCTCTCTCTCTCTTA[C/T]GGTTGGATTCCTTGA | 57626 |
rs57030417 | in-del | -/G | 0.251859 | 0.249993 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981227 | TATGACAATACTAAA[-/G]ATTACACTAAATATA | 57626 |
rs57038503 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69920096 | AAAACAATTTACAAT[A/T]TTGTATTATTATAAT | 57626 |
rs57110825 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69858693 | AAAATTTTTCTATTA[A/G]TGGAAATGACTATTG | 57626 |
rs57111056 | snp | A/G | 0.191461 | 0.24305 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966125 | TCATTGATGAAAGTG[A/G]CTACACTAAACAATA | 57626 |
rs57115450 | snp | C/G | 0.140919 | 0.224948 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834096 | AGGGGAGGGATGAAA[C/G]AGTGGAGGTTGAGGG | 57626 |
rs57184525 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69983620 | AGAAAAAAAAAAAAA[-/A]GCTGTGTTTGATGGT | 57626 |
rs57193410 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896865 | TTTAATAGAAACGGG[A/G]TTTCACCATATTGGC | 57626 |
rs57210446 | snp | C/T | 0.235564 | 0.249583 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000006 | CACATTCCTCATGAA[C/T]GGCTTGCTGCCATCC | 57626 |
rs57227774 | snp | A/G | 0.237593 | 0.249692 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004957 | ATCTACAAATATTAC[A/G]AGTAATTTTAATTAA | 57626 |
rs57276801 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896940 | CTCCCAATGTGCCGG[C/G]ATTACAGGTGTGAGC | 57626 |
rs57342083 | in-del | -/CC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896825 | AGGCGCACACCACCA[-/CC]TCACCTGGCTAATTT | 57626 |
rs57361427 | snp | A/G | 0.264358 | 0.249587 | intron-variant | KLHL1 | GRCh38.p7 | 13:69986959 | ATTAGATATCCAACA[A/G]TAAATAATATTTTAT | 57626 |
rs57365356 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69847413 | CATTAGCAAAAAAAA[A/G]AAAAAAAAAAAAAAC | 57626 |
rs57412615 | snp | C/G | 0.265453 | 0.249522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989404 | GGCAGTATGACTCCT[C/G]TAGATTTGTTCTTTT | 57626 |
rs57457553 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69743012 | ACATCAGTGAAGTTT[-/T]CAAAGAGATCCTGAA | 57626 |
rs57467526 | in-del | -/ACTGATATATTT | 0.499713 | 0.0119774 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968327 | TATCATGTAAATAGA[-/ACTGATATATTT]GCTAAGAAACAAATA | 57626 |
rs57637616 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103451 | ATGAGGGAGTGAGGG[A/G]TGTGGAAAAATATTT | 57626 |
rs57639697 | in-del | -/TTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947084 | TGTGTGAAGATCTTC[-/TTC]CTATTCCGTCACTGT | 57626 |
rs57681164 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882649 | AGAGGCTGTTAAGAT[G/T]AAAGCATTGTAATTG | 57626 |
rs57713566 | snp | C/G | 0.387263 | 0.208947 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793721 | ATTTTAGTTTCTGAA[C/G]GAGTAGAAAACTAGC | 57626 |
rs57717252 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092906 | GAACAGCGCAGCCAT[A/G]AAATAATTGCATCAT | 57626 |
rs57729265 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70093243 | ATGAAGTGAGGGAAA[-/A]TAGGAAAATCAAGAA | 57626 |
rs57740128 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769756 | CAGGTCTCCTTTTGT[G/T]GTTGAGAGCTATTCT | 57626 |
rs57751414 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752970 | GGTGGAATTACTAAT[A/G]CAGGCCCATTCTTTT | 57626 |
rs57764509 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69937261 | ATAATATTTAATTTG[A/G]ACAGAGAATTGCATT | 57626 |
rs57773730 | in-del | -/T/TTTT/TTTTTTT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027665 | TGTTTTTTTTTTTTT[-/T/TTTT/TTTTTTT]ATGAACTGAACAAAA | 57626 |
rs57793771 | snp | C/T | 0.373196 | 0.217538 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971658 | CTATCATATACTACT[C/T]ATTTCCTTATTTGAC | 57626 |
rs57793968 | in-del | -/GT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985883 | CCACTGTGTGTGTGT[-/GT]ATGTATATAAGTATA | 57626 |
rs57810678 | in-del | -/G | 0.499587 | 0.0143711 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019476 | ATTTGCTGATAGTGA[-/G]GGGGCTAGTGGGAGG | 57626 |
rs57826124 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896880 | GTTTCACCATATTGG[C/T]CAGGCTGGTCTCGAC | 57626 |
rs57828771 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960375 | CGTCTCACACCAGTA[G/T]GAAGAATTTAGGTAA | 57626 |
rs57856334 | in-del | -/AG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896906 | CGACTCCTGACCTCA[-/AG]TGATCCGCCCGCCTC | 57626 |
rs57874472 | snp | C/T | 0.107341 | 0.205301 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051819 | CTAACTTTTCAGAGA[C/T]TGATGGTAGACTGCT | 57626 |
rs57875323 | snp | C/T | 0.207253 | 0.246318 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004141 | AGTTTTTAACTGATA[C/T]TCTAAACAGAAATTT | 57626 |
rs57875746 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766623 | ATAAATATCCTTTGT[A/C]TTGTCAAGGAGGAAA | 57626 |
rs57906720 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936611 | AAAAAAAAAAAAAAA[-/A]TGAAGATTGAACATG | 57626 |
rs57912783 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780732 | ATATATATATATATA[-/TA]CATATATATATACAT | 57626 |
rs57923661 | in-del | -/CACACACACACACACACACACACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70082346 | ACACACACACACACA[-/CACACACACACACACACACACACA]AAGGAACCATAGTAG | 57626 |
rs57932607 | in-del | -/C | 0.191775 | 0.243125 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100182 | TGAATATTATATATT[-/C]ATATTTCTTCATTAT | 57626 |
rs58084035 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896829 | GCACACCACCACCTC[A/G]CCTGGCTAATTTTTG | 57626 |
rs58084677 | snp | C/G | 0.376791 | 0.215463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709505 | AAATATAGTGAGTAG[C/G]CTTTACTTGGATCCT | 57626 |
rs58156922 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980293 | TGTACAACAAATAAT[A/T]ACTCATGTGTTTTTT | 57626 |
rs58165303 | in-del | -/C | 0.499713 | 0.0119774 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968340 | GAACTGATATATTTG[-/C]TAAGAAACAAATATA | 57626 |
rs58218346 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001579 | CTATCTATGATCTAT[C/G]TGTCTATCTATCTAT | 57626 |
rs58269684 | snp | C/T | 0.326506 | 0.238006 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950526 | GAGTTTAACCTAAAA[C/T]AGCATGTCATGCAAC | 57626 |
rs58284665 | in-del | -/TT/TTT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960128 | TTTTTTTTTTTTTTT[-/TT/TTT]CAGGAAGCTTTTTTT | 57626 |
rs58298316 | snp | G/T | 0.326506 | 0.238006 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950293 | AAATTTACTTAAATT[G/T]CTTTAAAGCTACTCT | 57626 |
rs58329400 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69965012 | TTTAGTTCTTAGGCA[G/T]TGTTATTTGTTCTCT | 57626 |
rs58336790 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717715 | TCTTCGTTTACTCAA[G/T]AATTTAGCAGAGAAA | 57626 |
rs58344191 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878601 | ATATTAAATAAGCAA[C/T]ATATAATTATATGTT | 57626 |
rs58384249 | snp | C/G | 0.0310518 | 0.120672 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700346 | CTTCTAGCTGCTACA[C/G]TAGTCTCAGCACTCT | 57626 |
rs58396771 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730614 | GATCTTGCTCTATCA[C/T]CCAGGCTATAGAGCA | 57626 |
rs58414297 | snp | A/G | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839233 | TCATTCCTTAAAACT[A/G]GAAGTTTAATGTCTG | 57626 |
rs58430275 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810148 | GAGGCAGAAAACTAA[C/T]GAAGAAATTCTGGAC | 57626 |
rs58484758 | snp | G/T | 0.168785 | 0.236441 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712273 | TCATTTTTTTTTTTT[G/T]AAGGCGATCTCCTGT | 57626 |
rs58504097 | in-del | -/AAAAAAAAAAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69827742 | CTCAAAAAAAAAAAA[-/AAAAAAAAAAA]GTTATTCTTAGCACA | 57626 |
rs58522685 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885679 | CAAGAGGCCTGTATG[C/T]CTTTTGTACAATCTC | 57626 |
rs58550165 | snp | G/T | 0.251296 | 0.249997 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983628 | AAAAAAAAGCTGTGT[G/T]TGATGGTAAACTCCT | 57626 |
rs58606453 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | KLHL1 | GRCh38.p7 | 13:69977769 | CAAAATAAAAAATTC[A/G]GAGAGCCTTACCAGT | 57626 |
rs58655438 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961837 | ATTATGTTTTATTTG[C/T]CTGTTCTTGTGCCAA | 57626 |
rs58711996 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842070 | CACAAATGTAAGTTG[A/C]AAAACTATTAATATA | 57626 |
rs58765329 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736241 | AGGACATGAATAGAC[A/C]ATTCTCAAAAGAACA | 57626 |
rs58800073 | in-del | -/A | 0.396182 | 0.202807 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794564 | GAGATTAAAAAAAAA[-/A]GAGCTGGGGGAAGGA | 57626 |
rs58816551 | in-del | -/A | 0.472616 | 0.113763 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748794 | AGGATGGTCTGTCTT[-/A]GGGGTGGTCACTAAA | 57626 |
rs58820409 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100187 | ATTATATATTCATAT[A/T]TCTTCATTATGTGGC | 57626 |
rs58834027 | in-del | -/GTTT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961831 | TTTCTATTATGTTTT[-/GTTT]ATTTGCCTGTTCTTG | 57626 |
rs58864631 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936318 | TGGAGGCCTGGTGTG[A/G]TGGCTCATGCCTGTA | 57626 |
rs58869900 | in-del | -/CTTT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884938 | TTTTTCTTTTCTTTT[-/CTTT]TTTTTTTTTTTTTGA | 57626 |
rs58877477 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70059173 | TTTTTTTTTTTTTTT[-/T]CCTGAGATGGAATCT | 57626 |
rs58892254 | in-del | -/TAAAATAAAA/TAAAATAAAATAAAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69862024 | TAAAATAAAATAAAA[-/TAAAATAAAA/TAAAATAAAATAAAA]GCAAATACTTGAAGT | 57626 |
rs58927181 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898278 | GTAGAGCCCTGCAAA[C/T]TTTTACATGGACCTC | 57626 |
rs58965727 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827666 | ACCCCAGGAGTCAGA[C/G]GTTTCAGTGAGCCAA | 57626 |
rs58988338 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896852 | AATTTTTGTATTTTT[-/T]AATAGAAACGGGGTT | 57626 |
rs59017751 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993458 | GGTCACTCCTGGATT[C/T]TTTAGTTCAGGACTC | 57626 |
rs59070716 | snp | C/T | 0.253824 | 0.249971 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989135 | TTGAAATGATTTTTG[C/T]ATATAGTGTAAGGAA | 57626 |
rs59082732 | snp | G/T | 0.313814 | 0.241719 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958468 | TATAAACTATAATCA[G/T]TGAAGCTTATCTCAA | 57626 |
rs59093920 | snp | A/G | 0.265453 | 0.249522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989161 | AGGAAGGGGTCCAGT[A/G]TCACTTTTCTACATG | 57626 |
rs59113539 | snp | C/T | 0.314544 | 0.241524 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091520 | AATTTTCATTTATTT[C/T]TCTTGGGCAGCAAAA | 57626 |
rs59119291 | in-del | -/AAC/ACA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055024 | TTCAAAGACGTAATA[-/AAC/ACA]GAAATCTTTCCAAAC | 57626 |
rs59124157 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748909 | ACATCTCTAACTATA[A/G]TTAAATTAAATTGTT | 57626 |
rs59126736 | in-del | -/T/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69793495 | CTCATAAAATCATGT[-/T/TA]AAGTTTTTTTTTTAC | 57626 |
rs59128069 | in-del | -/AATAAAA/ATAAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70010928 | AAATAATAATAATAA[-/AATAAAA/ATAAA]TAAAATAAAATAAAA | 57626 |
rs59153814 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69772649 | GTCTTACTTTTAGAA[A/T]TTTTCTTTTAGAATA | 57626 |
rs59207074 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093831 | TTTAAATCCATTTGG[C/T]AATTAGAACTGCAGT | 57626 |
rs59252203 | in-del | -/AAA/AAAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69771292 | AAAAAAAAAAAAAAA[-/AAA/AAAA]CATGCTCTTCTTCTT | 57626 |
rs59297195 | snp | C/T | 0.14933 | 0.228835 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827674 | AGTCAGAGGTTTCAG[C/T]GAGCCAAGATCGTGC | 57626 |
rs59302694 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69757983 | AAAAAAAAAAAAAAA[-/A]TCACAGGCCATTGCA | 57626 |
rs59308887 | in-del | -/AAGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781002 | TTTTAGTAAGTAAGT[-/AAGT]TTCTTCCAGCATAAT | 57626 |
rs59311897 | snp | C/T | 0.265453 | 0.249522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989094 | TTTTATAGTTTTATG[C/T]TTTACATTTAAGTCT | 57626 |
rs59334541 | snp | A/C | 0.14933 | 0.228835 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827555 | GCCAACATGGTGAAA[A/C]CCCGTCTCTACAGAA | 57626 |
rs59338554 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734522 | TAGAACTAAGTCAAA[C/T]GAAAATTATTAAGAA | 57626 |
rs59374137 | snp | A/C | 0.318415 | 0.240457 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006167 | CCTGCAGGTTCATCT[A/C]TATTGTTGCAAATGA | 57626 |
rs59413734 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885864 | GTAATCAACTCTGTA[A/G]AATCCAGCTTTTCAA | 57626 |
rs59420221 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896839 | ACCTCACCTGGCTAA[-/T]TTTTGTATTTTTTAA | 57626 |
rs59453709 | snp | A/G | 0.265453 | 0.249522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987495 | GTATCACAAAGTAAA[A/G]ACATGTAAATAACTT | 57626 |
rs59483260 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896916 | ACCTCATGATCCGCC[C/T]GCCTCAGCCTCCCAA | 57626 |
rs59491613 | in-del | -/T | 0.185155 | 0.241444 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885425 | ATTATGTAGGTGTTA[-/T]TTTTTTTTTTTCTTT | 57626 |
rs59514285 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985921 | AAGTTATATATATAT[-/AT]GTAAATATATATGTA | 57626 |
rs59519359 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712498 | AGATTCTTTATATGT[A/G]TGATTTTGTTTCTGA | 57626 |
rs59525008 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770185 | GCATTCCCCTCAGCC[A/G]GATGCCAGCACCCAA | 57626 |
rs59580588 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741211 | TGGGAAGATATATAT[A/G]ACTAGTACTCATTGC | 57626 |
rs59598504 | in-del | -/A | 0.162581 | 0.234218 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024398 | AGAGAGAGATTGAGG[-/A]AAAAAACTCAGGGGA | 57626 |
rs59604067 | in-del | -/AA | 0.48818 | 0.0759629 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967886 | GCAAGATGCTGAATC[-/AA]AAAAAAAAAAAAAGA | 57626 |
rs59606834 | in-del | -/TGTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947071 | GTGTGTGTGTGTGTG[-/TGTG]AAGATCTTCTTCCTA | 57626 |
rs59614129 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954595 | ACACTGTGGTAGATA[C/T]ATAACCCTTACTCCT | 57626 |
rs59662277 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896894 | CCAGGCTGGTCTCGA[-/A]CTCCTGACCTCATGA | 57626 |
rs59683172 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69958739 | TCAAACCTTAAAATT[-/A]AAAAAAAAAAATACA | 57626 |
rs59717557 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734784 | AAACTTTAGAATATC[A/G]GTAAAATAGAATATT | 57626 |
rs59753241 | in-del | -/TAAAATAAAATAAAATAAAATAAAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69862000 | TAAAATAAAATAAAA[-/TAAAATAAAATAAAATAAAATAAAA]GCAAATACTTGAAGT | 57626 |
rs59765144 | snp | C/T | 0.326976 | 0.237854 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951319 | AGTGGCTTATTTTTT[C/T]TTTCCTTTATATTCT | 57626 |
rs59861641 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872486 | CTGAGAGGAGTTATA[G/T]CTTCATTACCATAAT | 57626 |
rs59924862 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885195 | TCCACCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 57626 |
rs59938855 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761676 | AATTACCAATGATAA[C/T]GCATTTAATAAATGT | 57626 |
rs59951451 | in-del | -/GTATAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69736690 | GTGAGATATATATAT[-/GTATAT]ATATATACACACACC | 57626 |
rs59958813 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985792 | TATATATATATATAT[-/AT]TTTATATATATTTAT | 57626 |
rs59988404 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900123 | ATATTTTCTGGAATA[C/G]ATGAATACTCTGGAT | 57626 |
rs60028692 | in-del | -/AC/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69954801 | ACACACACACACACA[-/AC/CA]TTTTAAACATATATA | 57626 |
rs60061703 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095725 | TTTTGAGAGGACAAT[A/G]AATTATTGTTAACTA | 57626 |
rs60067514 | snp | G/T | 0.354019 | 0.227333 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878713 | ATATATATATATATA[G/T]AGAGAGAGAGAGAGA | 57626 |
rs60096882 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70078758 | AAAAATGTGGTTTTT[A/T]AAAATTATAAATATA | 57626 |
rs60127818 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932359 | TTGTGGAAGACTGTG[C/T]TTTATAAGTTGAAAC | 57626 |
rs60134761 | snp | A/T | 0.265453 | 0.249522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989215 | CATTTATTGAATAGG[A/T]AATCCTTTCCCCATT | 57626 |
rs60137040 | snp | A/G | 0.455502 | 0.142369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793816 | TATATTTGAGAGCCT[A/G]ACATCATTTGTGACG | 57626 |
rs60156512 | snp | C/T | 0.250732 | 0.249999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980021 | TGACAAGGACATCAG[C/T]GTCTTTGTTGTGGCT | 57626 |
rs60167101 | snp | A/T | 0.364401 | 0.222289 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755649 | CTCCAAAGTAATTTT[A/T]AAAAAAAAGCACTGC | 57626 |
rs60195311 | snp | C/T | 0.321053 | 0.23969 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090972 | GGACTTCACATTACT[C/T]CTTCCTTTCTCTCTC | 57626 |
rs60288125 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708134 | CATGTATGCAGACTC[C/T]TATGGTAATGAAGCA | 57626 |
rs60307205 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003164 | ACAATTATGAGCATA[C/G]AAACTACAAATAAAT | 57626 |
rs60339895 | snp | C/T | 0.251859 | 0.249993 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981224 | ACATTATGACAATAC[C/T]AAAATTACACTAAAT | 57626 |
rs60422801 | in-del | -/TACACA/TATATATA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939379 | ATATATATATATATA[-/TACACA/TATATATA]CACACACACACGCAC | 57626 |
rs60435028 | snp | C/T | 0.264358 | 0.249587 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987297 | TCTGAGCTATGAGTA[C/T]TGCTTTATAAATTCT | 57626 |
rs60495432 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879737 | AACCAACCCTAAATA[A/T]AAAATTGTACTCTTT | 57626 |
rs60565370 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011320 | ATGAAACCTGTCAAC[A/G]CAGATATTATAAATT | 57626 |
rs60568513 | snp | C/T | 0.264906 | 0.249555 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987648 | AAGAACTCTTTTCCA[C/T]TGTTTTACCTAATGA | 57626 |
rs60572718 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896854 | TTTTTGTATTTTTTA[A/G]TAGAAACGGGGTTTC | 57626 |
rs60600073 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940462 | CAAATGCAGTTTCAA[A/T]CAACATATCTGTATA | 57626 |
rs60610351 | snp | A/T | 0.326506 | 0.238006 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951021 | TCAGATTTTAATATA[A/T]CAACACCTGTGTTTA | 57626 |
rs60613882 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001581 | ATCTATGATCTATGT[A/G]TCTATCTATCTATCT | 57626 |
rs60614038 | snp | A/T | 0.326506 | 0.238006 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949902 | TTGCAAATTTGTACC[A/T]CTTTATTGGCACTCT | 57626 |
rs60621173 | snp | A/G | 0.25045 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983924 | GACAAAGATCCCACA[A/G]TAAATGATGCTTGGA | 57626 |
rs60626476 | in-del | -/ATATGTATAT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020802 | GATATATATGTATAT[-/ATATGTATAT]GCATACATACACATA | 57626 |
rs60633551 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963878 | CTGATGGCAAAAAAT[-/A]AAAAAAACATACACA | 57626 |
rs60638539 | snp | A/G | 0.103082 | 0.202275 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853443 | CATGCTGAACTGTGA[A/G]TCGATTAAGCCTCTT | 57626 |
rs60660711 | snp | A/G | 0.31357 | 0.241783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950204 | TACAAGTCATTATTC[A/G]TTCTATTTCTGTCCA | 57626 |
rs60685343 | snp | A/C | 0.247337 | 0.249986 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987265 | AAAGGTAGTTACTTT[A/C]TTTTTAAAACAGAAA | 57626 |
rs60722059 | snp | A/G | 0.313082 | 0.241911 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945958 | TAAATAAACAAAATT[A/G]GAGTATGCTTATTCA | 57626 |
rs60756782 | in-del | -/GTGGCTCT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100198 | ATATTTCTTCATTAT[-/GTGGCTCT]TTCTTCTCAGCATGG | 57626 |
rs60804585 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70076401 | TCTTTTTTTTTTTTT[-/T]AATGGTTTTGGATCA | 57626 |
rs60808636 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | KLHL1 | GRCh38.p7 | 13:69702879 | AGAATAATTTTTATA[A/G]GTCACCACTCTTATC | 57626 |
rs60814075 | snp | C/T | 0.313082 | 0.241911 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943745 | TTAAACTGATTATAA[C/T]ACTTTTTTATTCATA | 57626 |
rs60822198 | in-del | -/TGTGTGTGTGTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947063 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTG]AAGATCTTCTTCCTA | 57626 |
rs60835886 | in-del | -/TAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69987007 | TTTTTAGATCATGAA[-/TAA]CAAGATAAAATATAT | 57626 |
rs60843307 | snp | C/G | 0.35445 | 0.227135 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095834 | TTCTCCCTCCACCCC[C/G]CCCACCACACTCGCT | 57626 |
rs60862183 | in-del | -/GAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936011 | TATAAGAAAGTTTAT[-/GAT]ATCACACAATCCTAA | 57626 |
rs60869989 | snp | A/G | 0.31357 | 0.241783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951421 | TTTCGCAAGTTAGTA[A/G]GAACATGTTTCTGTA | 57626 |
rs60883710 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884446 | AAAAAAAAAAAAAAA[-/A]CTACGTGAAGCTAAA | 57626 |
rs60920874 | in-del | -/A/AA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057805 | AAAAAAAAAAAAAAA[-/A/AA]GAAAGAAAGAAAAGA | 57626 |
rs60928151 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804307 | ATATAATTTTTTTGT[-/T]GGGGGGGGGAAATAG | 57626 |
rs60954548 | snp | A/G | 0.314301 | 0.241589 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956527 | TAAGCTACTCAAACT[A/G]TTTTGAGAGCAAGAC | 57626 |
rs60957671 | snp | A/G | 0.174932 | 0.238463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823110 | GAAAGAATTGCCACA[A/G]ATGAATAACATATGT | 57626 |
rs60970532 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048549 | ACAGGGACCAGTTTC[A/G]TGGAAAGCAATTTTT | 57626 |
rs61007948 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054829 | TGATCAAGCATTAAG[A/G]GAGAATTAGTGAGCT | 57626 |
rs61032367 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70010900 | CCGTCTCAAAAAAAA[-/TA]ATAATAATAATAATA | 57626 |
rs61036580 | in-del | -/A | 0.122411 | 0.214991 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849729 | CTTGCAGAAAATCAG[-/A]AAAAAAAATCTGCTA | 57626 |
rs61044491 | in-del | -/T | 0.457853 | 0.138915 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781103 | AGGACTGCCCAAATC[-/T]TTGCAGGGGGAGACA | 57626 |
rs61055870 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847422 | AAAAAAAAAAAAAAA[A/T]AAAAACATAATTTAA | 57626 |
rs61070599 | snp | C/T | 0.313326 | 0.241847 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951007 | ATGAAATATTTGTCT[C/T]AGATTTTAATATATC | 57626 |
rs61089671 | snp | A/T | 0.247337 | 0.249986 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987573 | GTGGAGTAAAGGGAA[A/T]GAGGGAAGGAGGGAC | 57626 |
rs61117808 | snp | A/C | 0.250732 | 0.249999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979874 | AACCATAGCTATACT[A/C]TTCTATTTCCTTTCA | 57626 |
rs61118704 | snp | A/T | 0.183568 | 0.241012 | intron-variant | KLHL1 | GRCh38.p7 | 13:69702926 | GTACTGTTATCTCCA[A/T]GAGAGAGATGAGTGA | 57626 |
rs61159451 | snp | A/T | 0.194902 | 0.243853 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962072 | TTGGGGAGACTTGAC[A/T]TAATTTTCATATAAA | 57626 |
rs61194858 | in-del | -/GTAGCCTC | 0.479583 | 0.0989539 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962783 | TTAATCAAGGCTATA[-/GTAGCCTC]ATAATATGAGCTGGG | 57626 |
rs61267522 | snp | C/T | 0.25045 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983754 | GCCTTGGTGACACAG[C/T]AAGCCCCTATTTCAA | 57626 |
rs61289215 | snp | C/T | 0.313326 | 0.241847 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950336 | ATCATTTGAAGAGAA[C/T]AAGGAATTGTTTTCA | 57626 |
rs61292957 | snp | A/C | 0.0648419 | 0.167978 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758358 | AAGATTTCCGTAAAC[A/C]TTTTATAAGTTCTTA | 57626 |
rs61330497 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038605 | TTTTTTTTTTTTTTT[-/T]GAGATAGAGTCTCAT | 57626 |
rs61379525 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70012910 | TCTGTATAAAAAAAA[-/T]AATAATAATAAATAA | 57626 |
rs61388440 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817050 | TGTGAGACTATTTTA[C/T]GTTTTCATCTTAAAA | 57626 |
rs61391357 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896887 | CATATTGGCCAGGCT[A/G]GTCTCGACTCCTGAC | 57626 |
rs61450154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883995 | GTATAAAAACTGCAG[C/T]AGAGTGACACTAAGA | 57626 |
rs61451843 | snp | C/T | 0.39979 | 0.200158 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780903 | TGTTTCCCTGACACA[C/T]GAGCATTTCTGGATA | 57626 |
rs61519423 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038369 | TTATGAACAATGGTG[C/G]ACAGGTTTTTATGTA | 57626 |
rs61543671 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69920097 | AAACAATTTACAATA[A/T]TGTATTATTATAATT | 57626 |
rs61579754 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001573 | GGATATCTATCTATG[A/T]TCTATGTGTCTATCT | 57626 |
rs61617598 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70010898 | CTCCGTCTCAAAAAA[-/T]AAATAATAATAATAA | 57626 |
rs61669127 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817196 | CCCTATGCCCCAGAA[A/C]AGGTCTTCCATATAA | 57626 |
rs61703547 | snp | A/G | 0.270621 | 0.249148 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821043 | AGACAACAGGTAAAC[A/G]AATAGGTGAAACCCA | 57626 |
rs61765952 | in-del | -/GCACATATTTGAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068488 | ATTTCTTATACAGTG[-/GCACATATTTGAG]TTTCAGACCCAAAGT | 57626 |
rs61963755 | snp | A/T | 0.125182 | 0.216612 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848530 | TCCTACTGACATAAC[A/T]ACTATTCTGGCCAAA | 57626 |
rs61963756 | snp | A/C | 0.320096 | 0.239972 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854692 | AATTAATGCCATTTG[A/C]ATTTATGAGTTTCTG | 57626 |
rs61963757 | snp | G/T | 0.293551 | 0.246177 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854810 | TTACCACAAAACACT[G/T]TTATATGTGAAGGCC | 57626 |
rs61963758 | snp | C/T | 0.428937 | 0.17459 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857271 | ACTTCTCTTCCAAGA[C/T]ACAACATATGTCACC | 57626 |
rs61963759 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858352 | AGTTTAATGAAAGAC[A/G]TAACTGTTAACCACA | 57626 |
rs61964160 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69934964 | TGTGTGTGCATGTGT[A/G]TATATATATATATAT | 57626 |
rs61964161 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69934966 | TGTGTGCATGTGTAT[A/G]TATATATATATATAT | 57626 |
rs61964162 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937119 | CTGACTTTGGAGGGA[A/G]GTAGCAATGATGACC | 57626 |
rs61964163 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945607 | AATTTTTAAAAAACT[A/G]GGCAAATGATTTATA | 57626 |
rs61964200 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997738 | TGTATTAATAAACAT[A/G]TTTATATTATATGAA | 57626 |
rs61964202 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004038 | ATACCTCTTAGACAT[A/G]GTTACTAGTTTATTC | 57626 |
rs61964203 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016951 | CCTGGGGGCCACCTG[C/T]CTGTGGAAAGAAGCT | 57626 |
rs61964216 | snp | A/T | 0.115088 | 0.210473 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025799 | AAAAGCAATTCTGAG[A/T]GAATAAATTGCCCTA | 57626 |
rs61964236 | snp | G/T | 0.492287 | 0.0616198 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033321 | TTGAGACAGAGTCTC[G/T]CTCTGTCGCCCAGGC | 57626 |
rs61964237 | snp | G/T | 0.488666 | 0.0744214 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033342 | TCGCCCAGGCTGGAG[G/T]GCAGTGGCGCGCTCT | 57626 |
rs61964238 | snp | A/T | 0.495634 | 0.0465208 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034980 | AATTTAAATAAAGTG[A/T]TTTTTGTAGTTACAA | 57626 |
rs61964239 | snp | A/G | 0.397813 | 0.201621 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036134 | TTTTATTTTACTTGA[A/G]AATAAATGACACACT | 57626 |
rs61964240 | snp | A/G | 0.110167 | 0.207236 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038485 | AGAAACTGCCAAATT[A/G]TTTTCCAGAGTGGTT | 57626 |
rs61964241 | snp | C/T | 0.408871 | 0.193029 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038747 | AGGCGCCCACCACCA[C/T]GCCTGGCTAATTTTT | 57626 |
rs61964242 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70047399 | AAAATGGAAATCTGT[G/T]TGTGTGTGTGTGTGT | 57626 |
rs61964245 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064215 | AAAAAAACCTTGATA[C/T]ATTTCTTGGATAAAA | 57626 |
rs61964246 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072817 | GGTAAAAAACTTTTA[A/T]TTAAAAAAAAACTAC | 57626 |
rs61964248 | snp | A/G | 0.197703 | 0.244469 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088194 | AAGTAGGATTGATAA[A/G]TACAAAATTGTATTA | 57626 |
rs61964249 | snp | C/T | 0.229429 | 0.249152 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097650 | AATTTTCTTTTTTAG[C/T]TCTGTTCAGAAATAA | 57626 |
rs61964561 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108866 | GCGTCAAAATGTGAC[G/T]ATGCCACCATCCTGA | 57626 |
rs61965328 | snp | A/T | 0.499999 | 0.000599041 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719211 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 57626 |
rs61965329 | snp | A/T | 0.48 | 0.0979796 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719213 | GTGTGTGTGTGTGAG[A/T]GAGAGAGAGAGAGAG | 57626 |
rs61965330 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751826 | TGCCAAATAATGTAC[A/G]TGAGAGGTGATAGTG | 57626 |
rs61965331 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757478 | TATTTGACAGTAGTC[C/T]CCATATAACTTAATA | 57626 |
rs61965332 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69788094 | CAACCATTGTGGAAG[A/T]CAGTGTGGCGATTCC | 57626 |
rs61965333 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816281 | TTTTTTTTTTTTTTG[G/T]AGACAGTCTCCCTCT | 57626 |
rs61965334 | snp | C/T | 0.030278 | 0.119257 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823205 | CTTACAACAACTTAA[C/T]ATGCAACCCTGTGCT | 57626 |
rs61965335 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824915 | AATTTTGCCTAAAAT[A/G]TCTAAAAAAAATTTG | 57626 |
rs61965336 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837083 | AAAATTTTTTTGACA[A/G]GACAGTAAGACTGGC | 57626 |
rs61965337 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844967 | TCGATCCAGGAAATA[C/T]TTGCTCCCGCAGGAT | 57626 |
rs61965352 | snp | C/T | 0.0154839 | 0.0868739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847929 | AATGTCTTATAAATA[C/T]ATCTAATACAAATAA | 57626 |
rs61965660 | snp | A/G | 0.43598 | 0.167067 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858698 | TTTTCTATTAGTGGA[A/G]ATGACTATTGATAAA | 57626 |
rs61965663 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69861610 | AACAAGTTTATGATT[C/T]CATATTTGGCCCACC | 57626 |
rs61965684 | snp | A/G | 0.34303 | 0.232046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864314 | ATTATAAGAAAAATC[A/G]TTAAATATGTATGTT | 57626 |
rs61965685 | snp | A/C | 0.290977 | 0.246619 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864599 | TTTTCAAATATAGTT[A/C]CTGGTTCAAAAAAAT | 57626 |
rs61965686 | snp | C/T | 0.434976 | 0.168179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864952 | GTTTTTGTTTTATTT[C/T]GTTTTGTTTTCAGAT | 57626 |
rs61965687 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876149 | ACTTATCAAGGAGTA[A/G]TTTGGGGAGGTAAAA | 57626 |
rs61965688 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877035 | AGAGCATAACTCTGT[A/C]CAAAAAAAAAAAGAT | 57626 |
rs61965689 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890882 | ATATTGCTTCTTTGC[A/G]TACATTTTAATCTTA | 57626 |
rs62962260 | in-del | -/AT/T | 0.130741 | 0.219721 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804298 | TGTAGACAAATATAA[-/AT/T]TTTTTTTGTGGGGGG | 57626 |
rs63258060 | in-del | -/TC | 0.493523 | 0.0565391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920112 | TTGTATTATTATAAT[-/TC]TCTGACTCAAATATA | 57626 |
rs63299960 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901795 | TCTTTTTCTTTTTTT[-/C]TTTTTTTTTTTTTTT | 57626 |
rs66482678 | in-del | -/TTC | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101271 | AATACAATATTGTCC[-/TTC]AACTAGCATGTTTCA | 57626 |
rs66489709 | snp | A/C | 0.391769 | 0.205917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792778 | ATGAAAGAAGCCATA[A/C]ACAAAAGGCCAGAAA | 57626 |
rs66490356 | in-del | -/GCTT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845268 | TAATAAAGTCTGCTT[-/GCTT]ATTACAAAACATATT | 57626 |
rs66492956 | multinucleotide-polymorphism | CA/TG | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025345 | TAGTTGACTTTGAGG[CA/TG]GAATTATTTTATGCA | 57626 |
rs66495562 | snp | A/C | 0.234692 | 0.249531 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075432 | ATAGAAAATTCCCAC[A/C]AAATTTTATTAAAAA | 57626 |
rs66548843 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70019366 | TGAGTAAGCTATAAA[-/G]AGTTAATGAAGGTCC | 57626 |
rs66587286 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815721 | AAAACTTTTTAAAAA[-/A]GCCGTAAATGAACTG | 57626 |
rs66591190 | in-del | -/GTTCTA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903508 | CCAAACCCTTTCTTC[-/GTTCTA]GTTCTCTAGAAAGCA | 57626 |
rs66892577 | in-del | -/GC/GTTTG | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964057 | CAGTTTGTTTGTTTT[-/GC/GTTTG]TTTAAAAATAGGCTC | 57626 |
rs66904675 | in-del | -/A | 0.0807149 | 0.183963 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732625 | AGACTAGAGGAGAGT[-/A]AAGGGTCTTGGTTTT | 57626 |
rs66906584 | in-del | -/CTC | 0.232943 | 0.249417 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090002 | TTTTACTGGCTTAAT[-/CTC]CTCTGAAAAGCCCAT | 57626 |
rs66915308 | snp | A/G | 0.455977 | 0.141681 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763794 | GCTAAATGCTTTGGA[A/G]TCAAACAGAAATGTT | 57626 |
rs66942404 | in-del | -/T | 0.490119 | 0.0695896 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004523 | ATCCTGCCATCCCCC[-/T]TGACTAGTCCACGTT | 57626 |
rs66953333 | snp | C/T | 0.428937 | 0.17459 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857227 | CCTTTACTTAAAAAC[C/T]CTCCTTCCTGAGTCC | 57626 |
rs66960703 | in-del | -/T | 0.137867 | 0.223442 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978504 | ATTCTGGTCAGAATA[-/T]TTTTTTTTTTTTTTT | 57626 |
rs66985863 | snp | C/T | 0.456095 | 0.141508 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770326 | GTGGGCAGAGTGAGC[C/T]GAGCAGGCATGAACA | 57626 |
rs67024946 | in-del | -/GTGTGTGTGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026704 | ATTTAAGAACTTAGG[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 57626 |
rs67045017 | in-del | -/A | 0.0364509 | 0.129988 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704972 | AGTACACTTAGTTGC[-/A]ACAATAGTTCTCAAT | 57626 |
rs67082157 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69753842 | GCATAGAAATAATTG[-/A]AAAAAAAAATTTTGA | 57626 |
rs67089042 | snp | A/G | 0.461923 | 0.132621 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808045 | TCAAAGTCCACCATA[A/G]GTTAATGAAAATGCA | 57626 |
rs67190517 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716998 | CTGTTCCATAAACTA[-/T]TCTAAAGTCCTCATT | 57626 |
rs67195697 | in-del | -/TATATA | 0.499053 | 0.0217445 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934963 | GTGTGTGTGCATGTG[-/TATATA]TATATATATATATAT | 57626 |
rs67243651 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69963212 | GACAGCATGCACAAC[-/G]CACCTCACCTAGCAT | 57626 |
rs67258245 | snp | A/G | 0.455024 | 0.143057 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800557 | GCAGGTATTGTAAAC[A/G]TTTTGTCTTCTTTTT | 57626 |
rs67297954 | in-del | -/TGCT | 0.211516 | 0.24702 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845263 | AGGTATAATAAAGTC[-/TGCT]TGCTTATTACAAAAC | 57626 |
rs67311577 | in-del | -/T | 0.167478 | 0.235987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886379 | GAAGTTTTGCACCAG[-/T]TTTTTTTTTGTTTGT | 57626 |
rs67327539 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075618 | ACTTACATATATATA[-/AT]TGTATATATATATAG | 57626 |
rs67352745 | in-del | -/GT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780716 | tgtatatatatatat[-/GT]atatatatatatata | 57626 |
rs67356407 | in-del | -/TTT | 0.255503 | 0.249939 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022600 | AGATTTGTTTTTAAA[-/TTT]TTACTATTTACATGA | 57626 |
rs67403546 | snp | C/T | 0.47885 | 0.100637 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793112 | AGATGTTGCATAGCA[C/T]ATAAAAAATCCATAA | 57626 |
rs67444969 | in-del | -/A | 0.474272 | 0.110462 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799094 | CTCAGTTGCATAAAG[-/A]AAAAAAAAAAAAGGT | 57626 |
rs67519504 | in-del | -/AATAA/ATAAA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010912 | ATAAAATAAAATAAA[-/AATAA/ATAAA]GAGCTCAGTATCAGT | 57626 |
rs67564403 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69866947 | ACCTAAATTATCACG[-/AT]TTTAATCATTACACA | 57626 |
rs67579189 | in-del | -/GT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780702 | TATATATATATATAT[-/GT]ATATATATATATATA | 57626 |
rs67612326 | in-del | -/T | 0.0752113 | 0.178743 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712761 | TTTGTTTGTTTTTTG[-/T]TTTTTTTTTTTGGGG | 57626 |
rs67650319 | multinucleotide-polymorphism | AC/GT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933095 | CATTGTCCCTTAAAC[AC/GT]TCATTATACTCACCC | 57626 |
rs67661890 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022281 | GATTACGTGTGTGTT[-/G]TGTGTGTGTGTGTGT | 57626 |
rs67679934 | in-del | -/TGTGTGTGTGTGTGAGAG | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719197 | ACGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGAGAG]AGAGAGAGAGAGAGA | 57626 |
rs67739818 | in-del | -/T | 0.0729998 | 0.176553 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715522 | AAGGCAGTTTTATTA[-/T]TTATTTTTTTTTTTT | 57626 |
rs67753156 | in-del | -/TTC/TTTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884936 | ACTTTTTCTTTTCTT[-/TTC/TTTC]TTTTTTTTTTTTTTT | 57626 |
rs67763269 | in-del | -/CATT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69950364 | GTAAAAGCAACATTC[-/CATT]CCTTGACTCACATCG | 57626 |
rs67787039 | snp | A/G | 0.454423 | 0.143914 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800372 | TTCTGGGCGGGGTGG[A/G]GGGAGGTGCATTATT | 57626 |
rs67809137 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69729523 | AACAAGGGGAAAAAA[-/A]TCACGTCAGCAGAGG | 57626 |
rs67831546 | in-del | -/T | 0.0494327 | 0.149241 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054824 | AAAATTGATCAAGCA[-/T]TAAGAGAGAATTAGT | 57626 |
rs67848439 | snp | A/G | 0.461592 | 0.133149 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808076 | AGTATAACACCAGCT[A/G]CTGAAGGCAACACCA | 57626 |
rs67866163 | in-del | -/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726516 | TTTCTTTCTAGTTGC[-/T]AAGAAATGATGGTGT | 57626 |
rs67908374 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817425 | GTTTTCCTTTTTCAT[-/A]AATGAGCACCCAACC | 57626 |
rs67934724 | snp | A/G | 0.44755 | 0.153212 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798855 | GGTGAATCATCTGAG[A/G]TCAGGAGACTGAGAC | 57626 |
rs68008540 | in-del | -/C | 0.151668 | 0.229849 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755726 | AACAAGATTATCTTG[-/C]CTCAGTCAGATGTAC | 57626 |
rs71116947 | in-del | -/TCTATCTA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789058 | CTATCTATCTATCTA[-/TCTATCTA]CTTATTTACCTACAT | 57626 |
rs71116950 | in-del | -/TA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833767 | ATATATATATATATA[-/TA]CATACATACATACAT | 57626 |
rs71116955 | in-del | -/CAGAGATAGAGATAGACAGTGATACAGATAGAGATAGAGA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855424 | AGATAGAGATAGAGA[lengthTooLong]CAGAGATAGAGATAT | 57626 |
rs71116956 | in-del | -/T/TT/TTA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895726 | CCTTTTTTTTTTTTT[-/T/TT/TTA]CAAGGTCTTGCTCTG | 57626 |
rs71116957 | in-del | -/AGTTCT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903513 | CCCTTTCTTCGTTCT[-/AGTTCT]CTAGAAAGCACTTTC | 57626 |
rs71116958 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903631 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTGTCGC | 57626 |
rs71116960 | in-del | -/AAAAAA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926970 | AAAAAAAAAAAAAAA[-/AAAAAA]GCAGAGAATTCACAC | 57626 |
rs71116961 | in-del | -/TG | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934956 | TACCGTGTGTGTGTG[-/TG]CATGTGTATATATAT | 57626 |
rs71116962 | in-del | -/TATATA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934983 | ATATATATATATATA[-/TATATA]TGTATATATATACAT | 57626 |
rs71116963 | in-del | -/CACTGGTGAACTTGGTACATAGTTCACC | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935262 | GGTACATAGTTCACC[-/CACTGGTGAACTTGGTACATAGTTCACC]TACTGGTGAACTTGG | 57626 |
rs71116964 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936593 | AAAAAAAAAAAAAAA[-/A]TGAAGATTGAACATG | 57626 |
rs71116966 | in-del | -/C | 0.4983 | 0.0291038 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959669 | GTAACTTTTTTTTTT[-/C]CCCCCAAAGGCCTGA | 57626 |
rs71116967 | in-del | -/ACAATTAATACT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960689 | AATACAATTAATACT[-/ACAATTAATACT]TGTATATTAACATTC | 57626 |
rs71116968 | in-del | -/GAGT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960709 | TAATACTTGTATATT[-/GAGT]AACATTCAACAAATG | 57626 |
rs71116969 | in-del | -/G | 0.479258 | 0.0997024 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963211 | GGACAGCATGCACAA[-/G]CCACCTCACCTAGCA | 57626 |
rs71116970 | in-del | -/GTTTG | 0.478698 | 0.105807 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964056 | TCAGTTTGTTTGTTT[-/GTTTG]TTTTAAAAATAGGCT | 57626 |
rs71116971 | in-del | -/TCTA/TCTATCTA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001617 | CTATCTATCTATCTA[-/TCTA/TCTATCTA]CCTATCATCTTTCTA | 57626 |
rs71116972 | in-del | -/T/TATC/TATCTATC/TATCTATT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001697 | ATCTATCTATCTATC[-/T/TATC/TATCTATC/TATCTATT]ATCTTTCTACTATCT | 57626 |
rs71116977 | in-del | -/G | 0.327445 | 0.237702 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019365 | CTGAGTAAGCTATAA[-/G]AAGTTAATGAAGGTC | 57626 |
rs71116978 | in-del | -/GT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022304 | TGTGTGTGTGTGTGT[-/GT]ATGTGTTTGGTTGTA | 57626 |
rs71116979 | in-del | -/TTCTCTCTTTCTCTCTCTCTCTCTCTCT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024637 | TCTCTCTCTCTCTCT[-/TTCTCTCTTTCTCTCTCTCTCTCTCTCT]CTCTCTCTCTCTCTC | 57626 |
rs71116980 | in-del | -/GTGTGTGT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026704 | ATTTAAGAACTTAGG[-/GTGTGTGT]GTGTGTGTGTGTGTG | 57626 |
rs71116981 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033637 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 57626 |
rs71116986 | in-del | -/AT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075627 | CTTACATATATATAT[-/AT]GTATATATATATAGG | 57626 |
rs71116987 | in-del | -/TA/TATA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075773 | ACATATATATATATA[-/TA/TATA]CATATATATGTATAT | 57626 |
rs71116988 | in-del | -/CTTTTT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084623 | GCCACCACGCCAGGC[-/CTTTTT]TTTTTTTTTTTTTTT | 57626 |
rs71196261 | multinucleotide-polymorphism | AT/TC | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714865 | TCCAAAGGTGCCAGT[AT/TC]TACAGGTGTGAGCCA | 57626 |
rs71196263 | in-del | -/TT | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764929 | CATGTATATCTTTGC[-/TT]TTTTTTTTTTTTTTT | 57626 |
rs71196264 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815710 | CCGTGGAATCTAAAA[C/T]TTTTTAAAAAGCCGT | 57626 |
rs71196265 | in-del | -/A | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827730 | GCGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 57626 |
rs71196266 | in-del | -/TATA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833748 | ATAAAGAAATAATGG[-/TATA]TATATATATATATAT | 57626 |
rs71196268 | in-del | -/AAAAT | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861965 | GCGAAACTCCGTCTC[-/AAAAT]AAAATAAAATAAAAT | 57626 |
rs71196269 | in-del | -/AAAAGAGGATCCTAGAAGAAGACTAGGCACCAGT | 0.434398 | 0.168811 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863387 | ACAGAGAATTAAAAC[lengthTooLong]AAAATATTAAGGTCT | 57626 |
rs71196271 | in-del | -/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909679 | GGGTCTTAAAAATAA[-/T]TTTTGGAAAAGACCC | 57626 |
rs71196272 | in-del | -/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027638 | GGCATTTTTGAAGCG[-/C]CAAAATGTAAGTTTT | 57626 |
rs71216506 | in-del | ATG/TA | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855867 | TGTTATATAATATAT[ATG/TA]TATATTATATATGTT | 57626 |
rs71216507 | in-del | -/CA | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861805 | AAAAAAAAAAAAAAA[-/CA]AAATACAAAATTAGC | 57626 |
rs71216508 | in-del | ATATGGGTGAGGCCC/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862699 | ATACTAAATGAGGTA[ATATGGGTGAGGCCC/T]TAATGCAATAAGACT | 57626 |
rs71303733 | multinucleotide-polymorphism | CAA/TAT | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721072 | ATATATATATATATA[CAA/TAT]ATATATAAAGCTATG | 57626 |
rs71303734 | in-del | CAGATAGATACATAGAGAGATAGATCTATAGATAGAGATAGAGATAGATAGA/TACATAGAGAGATAGATCTATAGATAGAGATAGAGATAGACAGAGATACAGATAGAGATAGAGACAGAGATAGAGATAGACAGT | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855404 | AGATAGATAGATAGA[lengthTooLong]GATACAGATAGAGAT | 57626 |
rs71415695 | multinucleotide-polymorphism | CT/TG | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915239 | CAGAATTGGAAAAAA[CT/TG]ACTTTCAAGTTCATA | 57626 |
rs71429617 | snp | C/T | 0.412249 | 0.190198 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715515 | CCAGTCTAAGGCAGT[C/T]TTATTATTTATTTTT | 57626 |
rs71429618 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719197 | ACGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGAG | 57626 |
rs71429619 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764756 | CGACTCAATTCTATT[C/T]TGAATTTTAAGAAGA | 57626 |
rs71429620 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808738 | GAAATGTCTGTAATG[A/C]CAGATATAGAATTAA | 57626 |
rs71429621 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849480 | AGCCAAGCACATTCA[A/T]GCTCTCTTTCTCTCT | 57626 |
rs71429622 | snp | A/T | 0.300169 | 0.244914 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857854 | AGTATAATATAAAAA[A/T]ATATATATATAATGA | 57626 |
rs71429623 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901572 | AATGGGTTTAGGGAC[A/C]AGAGTATTTTCAGTC | 57626 |
rs71429624 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907930 | GGAGTGAAGAAAAGG[A/G]AGAATCTATTTCAGC | 57626 |
rs71429625 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909160 | AAGTGGATGCTCAAG[A/C]CAGAAAGAGAGAGAG | 57626 |
rs71429627 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938752 | AAAATTTCTAAAGAA[A/G]GATTTGCCAATAGAA | 57626 |
rs71429628 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973890 | TTTTGCCAAGCAAAA[A/C]CCAACTCAGAGTAAT | 57626 |
rs71429629 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979711 | CTTTATTTTGGCCCA[A/C]CAATACAAAGCTTGA | 57626 |
rs71649391 | in-del | -/TG | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730288 | GTACTAACACTTTAA[-/TG]TGTGTGTGTGTGTGT | 57626 |
rs71659989 | in-del | -/T | 0.492823 | 0.0594727 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036836 | TTTAATGCCATGGTC[-/T]TTTTTTTTTTTTTTT | 57626 |
rs71688236 | in-del | -/CAAA | 0.461481 | 0.133325 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808868 | TGTATTGGAAAGAAC[-/CAAA]CAGATTTTCTGCAAT | 57626 |
rs71693665 | in-del | -/TTAAAAAAAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69975505 | ACAACAACAAAAAAC[-/TTAAAAAAAT]GTGAATCCTTATTTC | 57626 |
rs71699334 | in-del | -/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69954810 | GTTTTACACACACAC[-/CA]ACACACACATTTTAA | 57626 |
rs71704752 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69808552 | TAAAAAAAACAGAAT[-/A]AAAAAATCAAGAAGT | 57626 |
rs71707367 | in-del | -/A | 0.385932 | 0.209815 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086281 | TTTCAAAAAAAAAAA[-/A]GTAGACCTGGCTGGG | 57626 |
rs71718305 | in-del | -/TTA | 0.467946 | 0.122472 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745304 | TTAATTGGATGTCTC[-/TTA]TTATTAATTATATCA | 57626 |
rs71813182 | in-del | -/TG | 0.191147 | 0.242974 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985872 | TACATAGTATTCCAC[-/TG]TGTGTGTGTGTATGT | 57626 |
rs71815356 | in-del | -/TTGT | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728405 | ACTGCCTTGTAAAAA[-/TTGT]TTTGTTTGTTTGTTT | 57626 |
rs71853482 | in-del | -/ATAAG | 0.164219 | 0.234823 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827287 | ATGTTTTCTAAAATC[-/ATAAG]ATAAGGTTTATTTAG | 57626 |
rs71896706 | in-del | -/AGTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69841210 | AGTATTGGAAGTCTT[-/AGTC]AGAACAATCAGGAAA | 57626 |
rs71966264 | in-del | -/GTGTGTGTGTGTGTGAGA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719196 | TACGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGAGA]GAGAGAGAGAGAGAG | 57626 |
rs72007331 | in-del | -/TA | 0.445724 | 0.155538 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773864 | GAGAAAGTCCTTGGC[-/TA]TATATATATATATAT | 57626 |
rs72123116 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780746 | TACATATATATATAC[-/AT]ATATATATATACACA | 57626 |
rs72187113 | in-del | -/CAAAAA | 0.493613 | 0.0561475 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068340 | AGCGAGACTCCGTCT[-/CAAAAA]CAAAAACAAAAACAA | 57626 |
rs72302649 | in-del | -/AAAAGAGGATCCTAGAAGAAGACTAGGCACCAGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69863388 | CAGAGAATTAAAACA[lengthTooLong]AAATATTAAGGTCTG | 57626 |
rs72342329 | in-del | -/ATGGGTGAGGCCC/GAGTCCC/TATGGGTGAGGCCC | 0.434543 | 0.168653 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862699 | TACTAAATGAGGTAT[lengthTooLong]TAATGCAATAAGACT | 57626 |
rs72434195 | in-del | -/ACAATTAATACTTGTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69960689 | AATACAATTAATACT[-/ACAATTAATACTTGTA]TATTGAGTAACATTC | 57626 |
rs72493464 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69831089 | GTAGAAGAAAAAAAA[-/AA]TAACAAAGATCAGAG | 57626 |
rs72522948 | in-del | -/T | 0.348794 | 0.229651 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793494 | TCTCATAAAATCATG[-/T]TAAGTTTTTTTTTTA | 57626 |
rs72522950 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69809019 | AAAAAATAAAGTAAA[-/A]AGAATTTCAAAACAT | 57626 |
rs72522951 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69866945 | TGACCTAAATTATCA[-/AT]CGTTTAATCATTACA | 57626 |
rs72522952 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69943245 | ATTTCTTCATTTAAT[-/C]TTTTTTATAATTAAA | 57626 |
rs72573818 | in-del | -/CTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69709660 | ATTAAAAAATAAAGT[-/CTT]CMTTATTTTTGTTTG | 57626 |
rs73210440 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69702106 | ATTTCATAGTGATAG[C/T]TTGGAGTATATTTTA | 57626 |
rs73210442 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705368 | AAACTGTTAATCGAT[C/T]CCTAATCTATTTCCA | 57626 |
rs73210445 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711394 | TTCAAAAGAATGGCA[C/T]ATAGATTTCAAGTAC | 57626 |
rs73210461 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730685 | CAAGTAATCCTCTCA[C/T]CTCAGCCCCTCAGCC | 57626 |
rs73210463 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731535 | TCTCAGCAACTATAG[C/T]CAAAAGAAGTCTAGC | 57626 |
rs73210469 | snp | A/T | 0.132409 | 0.220618 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746076 | CATTTGATTTCCCTA[A/T]GCTATTGCAATTGGC | 57626 |
rs73210470 | snp | A/C | 0.131038 | 0.219882 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746116 | TTTTCTATTTGTTTC[A/C]TCAATAAATAAAAAG | 57626 |
rs73210474 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751685 | TATGCCAATATGATT[C/T]ATTTTATCCTAAGAG | 57626 |
rs73210481 | snp | A/C | 0.381891 | 0.212379 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756972 | AAACAAACAAAAAAA[A/C]CTCCAGTTATTAGGC | 57626 |
rs73210482 | snp | C/T | 0.391024 | 0.206427 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757044 | TTGTCCTGCTTTGGT[C/T]AGCATTTTTTATAAA | 57626 |
rs73210485 | snp | G/T | 0.380529 | 0.213219 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762749 | CTGCCATCATGAGAC[G/T]CTTACCTCAATTTTT | 57626 |
rs73210500 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791870 | ATGAACATAGATTAG[A/C]AAATAATTTTTTGGA | 57626 |
rs73210502 | snp | C/T | 0.448066 | 0.152544 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793998 | CAGAACTTGCCAGAA[C/T]TGGATTGTTAACATC | 57626 |
rs73212509 | snp | C/G | 0.440746 | 0.161604 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800336 | TATTCACAGGTTCCA[C/G]GGTTTAGGATATGGA | 57626 |
rs73212512 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804310 | ATAATTTTTTTGTGG[C/G]GGGGGGAAATAGTAA | 57626 |
rs73212516 | snp | A/C | 0.333722 | 0.235565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805557 | GAATACAAGTCAATA[A/C]AATATTTAAATAAAA | 57626 |
rs73212517 | snp | A/C | 0.456803 | 0.140473 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805697 | GAAAAAAAACAAAAA[A/C]AAAAACAAAACAACA | 57626 |
rs73212518 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808386 | CATCACCAGACAAAA[A/T]TACATTACTACAACC | 57626 |
rs73212520 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822642 | GAGACACTTACAAAA[A/C]TATTACAAGTTATGT | 57626 |
rs73212525 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849688 | ATGTAGTCACTTAAA[A/G]GCTTAAAAATATGCT | 57626 |
rs73212526 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849975 | ATGTCTATTAGAAAC[C/T]TCTTTGCTAAACAAT | 57626 |
rs73212531 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883838 | TACATGTTTAGAGAA[A/G]ACAGAGATTCTGCTG | 57626 |
rs73212532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888286 | TTAGGTTTTAACATA[C/T]GGAATTTGGGGGGAC | 57626 |
rs73212535 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69899409 | AAATTGTGTGGCAAG[C/G]TCATCCTCTGCATAA | 57626 |
rs73212539 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919080 | GTGGTCTACCTTGTC[C/T]AACACCATAATGGTC | 57626 |
rs73212542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920739 | ATGCTCTCGTTCAAA[G/T]AAGTTTTCCATTCAC | 57626 |
rs73212550 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945270 | GAGCCACTGCACCCG[C/G]CAGCTATAAAACTTC | 57626 |
rs73212551 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952114 | TATGTTTTGTTTAAC[G/T]GAATCTGGCAAATAA | 57626 |
rs73212571 | snp | C/T | | | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69994758 | TAAGCCTCTATTAAT[C/T]GGAGTTCTAGAATCT | 57626 |
rs73212576 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007156 | AACTTATCAACAAAC[C/T]GTGATAATACAAATC | 57626 |
rs73212590 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024335 | ATAACCATAACACTT[C/T]TGAATTGTAAGACCT | 57626 |
rs73214609 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036515 | TTTTAGTACACATAC[A/G]TATGTGTGTATGGGT | 57626 |
rs73214616 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040881 | AATATTTGATATTTC[A/T]TTGTATCCTACATGT | 57626 |
rs73214623 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054586 | AGTATGAGTGACCAA[A/C]CCCCAAGTGACATAA | 57626 |
rs73214640 | snp | A/C | 0.324619 | 0.238604 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078189 | GGGAATTAACTCAAT[A/C]AAAAAAAAAAAGTAT | 57626 |
rs73214641 | snp | C/T | 0.143284 | 0.226079 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079391 | AACCCATGGCATGTA[C/T]GCTATGGTAAGTACC | 57626 |
rs73214642 | snp | A/G | 0.104859 | 0.203554 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080382 | GATAATTAGAGGAAC[A/G]ATCTTTAAAATTAAG | 57626 |
rs73214656 | snp | A/T | 0.318266 | 0.240499 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100399 | TGCTAAGCTTGCTAC[A/T]TTTTTTTGTCGATTT | 57626 |
rs73504006 | snp | A/T | 0.128288 | 0.218372 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746123 | TTTGTTTCATCAATA[A/T]ATAAAAAGAAAATAG | 57626 |
rs73504022 | snp | A/G | 0.118584 | 0.212673 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757396 | TTTTAGGAACCTTGT[A/G]AAATTTTGGAACACA | 57626 |
rs73504023 | snp | C/T | 0.148661 | 0.22854 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757768 | ACCAGCCTGGCCAAA[C/T]CCCATGGTGAAATCT | 57626 |
rs73504028 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760261 | ATTGAGAGCCTCAGC[C/T]GAGGACCTACCTTTT | 57626 |
rs73504029 | snp | A/C | 0.078151 | 0.181571 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763117 | CCCTCATAAAAAGTT[A/C]TATAGCAGATTCTAC | 57626 |
rs73504065 | snp | A/G | 0.391954 | 0.205789 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793078 | GCAGAAACAACCCCT[A/G]CCATATATTTAATAT | 57626 |
rs73504077 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800353 | GTTTAGGATATGGAC[A/G]TTTTTCTGGGCGGGG | 57626 |
rs73504081 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800843 | CTTAGAGAAAAACCA[A/G]TATTTATCATAATAT | 57626 |
rs73504085 | snp | A/G | 0.153332 | 0.230554 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801075 | CTACCTAAAGCCCTC[A/G]ATGGACCACAATGTA | 57626 |
rs73504090 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802015 | AAGTATTTGTCCCCT[A/T]GCCCCCCTACCCCCT | 57626 |
rs73504094 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804735 | AACAACAGCAACAAA[C/T]GATAAAATCCATATT | 57626 |
rs73504095 | snp | A/G | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805993 | GTATATAACTATAGC[A/G]TTTTCTTTAAACAAA | 57626 |
rs73504098 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806645 | ATCAGCTTTAACAAT[C/G]TGGGCCATGGGAGAA | 57626 |
rs73506309 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811833 | AGTCCATCAGTTTTG[C/T]TGATGTTTTCAAAAA | 57626 |
rs73506314 | snp | G/T | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815603 | AACTATCATCCATCA[G/T]GTACTATGTTTACTC | 57626 |
rs73506320 | snp | A/G | 0.115438 | 0.210697 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816890 | CTGAACCCAGGAGGC[A/G]GAGTTTGCAGTGGGC | 57626 |
rs73506321 | snp | G/T | 0.45574 | 0.142025 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816894 | ACCCAGGAGGCAGAG[G/T]TTGCAGTGGGCCAAG | 57626 |
rs73506327 | snp | C/G | 0.175254 | 0.238565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818093 | GTAAAAGAAAACTTC[C/G]CTTTTCATCTGACAG | 57626 |
rs73506335 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824848 | ATACCTGTATGCATT[A/G]TGAAAACTCACTTAA | 57626 |
rs73506336 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828268 | GCTCACCTCACTGAG[A/G]GAACCTGAAAATCCA | 57626 |
rs73506344 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841836 | GTATTTCTCTAAAGA[C/T]AGATATATAGGCCAA | 57626 |
rs73506390 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855404 | GATAGAGATAGATAG[A/T]GATACAGATAGAGAT | 57626 |
rs73508421 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861746 | TGAGGTCGGGAGTTC[A/G]AGATCAGCCTGACCA | 57626 |
rs73508445 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866932 | AGGGAAACATTTTCT[G/T]ACCTAAATTATCACG | 57626 |
rs73508456 | snp | G/T | 0.315516 | 0.241263 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868048 | ATAATCAAATTTAAA[G/T]AATTTTGGAAAAAAT | 57626 |
rs73508462 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870196 | TTTAGGTAAGTCTCA[A/G]GATGCTGCCACTCGT | 57626 |
rs73508464 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870947 | CTTCCAGGCTGAGGT[A/G]CAAACTGCCAGTGTC | 57626 |
rs73508468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871902 | AAAAATTTCCCTCAT[A/C]TTGCTTTATTTTTTA | 57626 |
rs73508470 | snp | G/T | 0.377854 | 0.230241 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872872 | ATTCATGAGGGATCC[G/T]CCCCAATGACACAAA | 57626 |
rs73508478 | snp | G/T | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880981 | CCCAAAAGATTACCC[G/T]CCCAAACTCTAATAG | 57626 |
rs73508479 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880986 | AAGATTACCCGCCCA[A/G]ACTCTAATAGATACT | 57626 |
rs73508484 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882731 | GGATTATAATGCTGA[A/G]CTTTGTTATGCAGGC | 57626 |
rs73508486 | snp | G/T | 0.0923359 | 0.194016 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884485 | GAGGAATCTTTGAAA[G/T]ATTTGTCCACCTGTT | 57626 |
rs73508490 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896585 | TTAGTCATTCAATAC[A/G]AATGTATCATATATG | 57626 |
rs73508496 | snp | A/G | 0.218151 | 0.247963 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899332 | GAAGTATACATGGGG[A/G]TAAGAATGCTGGGAA | 57626 |
rs73508498 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900155 | TGGGTTTGCCTCTAT[A/G]CCCTTCAATAACATC | 57626 |
rs73508500 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903313 | TATCTCACAGAGATT[C/T]CTGGTTCGAGGCTTG | 57626 |
rs73508501 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907261 | CATTTTAGATGAACC[A/G]TGGGTATAAAAGCAA | 57626 |
rs73510103 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908398 | GGTGTGAGAGAAGAT[C/T]TGACAAAAAAAGTTC | 57626 |
rs73510109 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910903 | ATGAATTTGTTAGCA[A/T]ATGAAAAAGTGACTT | 57626 |
rs73510113 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911482 | AGGGGTTATGTTAAT[A/G]GATTCTCTTTACAAA | 57626 |
rs73510149 | snp | G/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935556 | GAGTTTTCAGAGAAT[G/T]AGTCTCTGTAGAAGT | 57626 |
rs73510151 | snp | C/G | 0.0952156 | 0.196321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935730 | AGATCAGTGTGGCTA[C/G]AACTGTATGAACAGG | 57626 |
rs73510152 | snp | A/T | 0.0952156 | 0.196321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935772 | CAGAAAATGTGATTT[A/T]AAAAATGTCAAAGGC | 57626 |
rs73510162 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937846 | TAAAGTCTGGGTAGA[C/G]CAGACCTTTGGTCTT | 57626 |
rs73510166 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943015 | ATGTTGGTGAAGAAT[C/T]CATACTAGTTGTTCT | 57626 |
rs73510168 | snp | A/G | 0.132409 | 0.220618 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943618 | CTATAGGTTACAGAA[A/G]CCTATATTTGTATAT | 57626 |
rs73510171 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944616 | AGAAGCTCAAAGATC[A/G]ATATTGCTAAGATTT | 57626 |
rs73510173 | snp | G/T | 0.333528 | 0.240328 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944948 | AAAATGGATCACGAA[G/T]CTAAATTCAAACATT | 57626 |
rs73510178 | snp | A/G | 0.312837 | 0.241974 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945121 | CTCCCAGGTAGCTGG[A/G]ATTACAGTCACCCGC | 57626 |
rs73510184 | snp | C/T | 0.313082 | 0.241911 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946173 | ACTGATGCTTATGTA[C/T]TAGGTGGGGATAAGG | 57626 |
rs73510188 | snp | A/G | 0.31014 | 0.242659 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946556 | CTTATTCTGTCATCT[A/G]GGCTGAAGGGCAGTG | 57626 |
rs73510190 | snp | C/G | 0.31014 | 0.242659 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946590 | TGATCCTAGCTCACT[C/G]CATGCTTGAACTCCT | 57626 |
rs73510191 | snp | A/C | 0.341685 | 0.232581 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946767 | ATCCTCTTGCTCTGG[A/C]CTCCCAAATTGTTGT | 57626 |
rs73510192 | snp | C/T | 0.310386 | 0.242597 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946821 | GCCTGGCCAATAATT[C/T]TTCTGAATGTTTGCA | 57626 |
rs73512608 | snp | A/G | 0.326741 | 0.23793 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948551 | GTGCTACATTTATCT[A/G]CAATCACATCTTAAG | 57626 |
rs73512624 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950912 | ATTCGTTGTTATATC[A/C]ACTTTTGGCTAAATA | 57626 |
rs73512626 | snp | A/C | 0.314544 | 0.241524 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952718 | TTCAACTGAGGGAGA[A/C]AAAGTGTTTAAAATT | 57626 |
rs73512630 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956903 | GAAAACGTTCGTCTG[A/T]AAAATGTATAATGTT | 57626 |
rs73512654 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964652 | AATGCTACATAGACT[A/G]TTCAATCTTAATTCA | 57626 |
rs73512660 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966383 | CTATAAAGCCTGGAC[A/G]ACAGCACATCGTTTG | 57626 |
rs73512667 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973013 | TTGGGCTATTTGTGA[G/T]AAAGTGATATTCCTC | 57626 |
rs73512674 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976939 | TAGTTATTAACAACA[C/T]AGAGTGAGAGTCCAA | 57626 |
rs73512685 | snp | A/G | 0.234109 | 0.249494 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981703 | TACCTTTTAAAAAAT[A/G]TTCACATATTTTATA | 57626 |
rs73512687 | snp | C/T | 0.251296 | 0.249997 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981728 | TTTATATCAGGCACA[C/T]ATTATTTTAAACAAC | 57626 |
rs73512695 | snp | A/G | 0.25045 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984013 | GTCAACTAAAAATAG[A/G]TTAGAGTCTTAAATG | 57626 |
rs73512697 | snp | C/T | 0.25045 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984234 | GTAAGGTTTCTCTTT[C/T]AATAAAAAGCAGCCC | 57626 |
rs73512702 | snp | A/C | 0.25045 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984253 | AAAAAGCAGCCCCCA[A/C]ATCATTTCTTTTCTG | 57626 |
rs73514705 | snp | A/C | 0.25045 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984301 | AAATCGAGCTGCAGA[A/C]ATAGATAAGCAAACT | 57626 |
rs73514707 | snp | A/G | 0.192088 | 0.2432 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984529 | TTGAGCTAGGTAAAT[A/G]TCACACCTGGTCCAA | 57626 |
rs73514712 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985147 | CAACAACAACAACAA[A/C]AAACCTCTGTGCAAA | 57626 |
rs73514715 | snp | A/T | 0.264084 | 0.249603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985485 | TATCAAAAAGAAAAA[A/T]ATATATAAAAAATAC | 57626 |
rs73514719 | snp | A/G | 0.26326 | 0.249648 | intron-variant | KLHL1 | GRCh38.p7 | 13:69986307 | TTTATTACATATTTC[A/G]AAATAGCAAGAAGAG | 57626 |
rs73514723 | snp | C/T | 0.264084 | 0.249603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69986811 | GAAGTGATGTCAAGA[C/T]ACTTGATGTGTTTAA | 57626 |
rs73514736 | snp | A/C | 0.264632 | 0.249571 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988767 | TATGTCTTCCTTTGA[A/C]AAGTGTCTTCATGTC | 57626 |
rs73514752 | snp | A/G | 0.246485 | 0.249975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991215 | TTAGAAAGGTCTCAA[A/G]TTAACAACCTAACAT | 57626 |
rs73514757 | snp | A/T | 0.246485 | 0.249975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992245 | TTGCCACAAATGTAT[A/T]GAGTGCCTACTCTCA | 57626 |
rs73514793 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014694 | ATCAATGTACTTAAA[G/T]AATTGCACTTATAAT | 57626 |
rs73516708 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020631 | AGCTGTACCTTTTAT[A/C]TATGATTCCCAGGGC | 57626 |
rs73516783 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044801 | CTTTATCATTAAGAA[C/G]AAATGTTCCTGCATC | 57626 |
rs73516785 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045063 | GTCATTTTGAAGATG[A/T]TTATATACACATAGT | 57626 |
rs73516787 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046598 | GCTCAAGCGATTCGC[A/G]TGCTTCAGCTTCCCT | 57626 |
rs73516789 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046903 | GGAAATTGTTTTGCT[C/T]GAGATTATTGTATTT | 57626 |
rs73516793 | snp | C/G | 0.0584853 | 0.160693 | intron-variant | KLHL1 | GRCh38.p7 | 13:70049215 | CAAGAAAGTTTAGAT[C/G]AGTAAACATCATAGA | 57626 |
rs73516798 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055305 | AAGGAAAAAATATTT[C/T]ATCCTAAAAAAGTAT | 57626 |
rs73518704 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061031 | CTAAAATTAAAACAA[C/T]TGATCTCAGGGAGAT | 57626 |
rs73518730 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080912 | CTACCATTTTAAAAG[A/T]TGATTTTCTGGTCAT | 57626 |
rs73518733 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082405 | TGCTCTAGGTGGATA[C/T]AGACTTGGGATTTAA | 57626 |
rs73518771 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102082 | TAGTTTGAGAACCAC[A/G]TTCCTGAGAAAGTAG | 57626 |
rs73518774 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105237 | AAATAATAAACTATT[C/T]TCAAAAGTAAGAAAC | 57626 |
rs73518776 | snp | A/T | 0.0839998 | 0.186933 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105247 | CTATTTTCAAAAGTA[A/T]GAAACTTGTTAAGTC | 57626 |
rs73520082 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703221 | AAATTCCATCGTCTG[A/G]TAATGTCATAGCCCT | 57626 |
rs73520083 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705066 | CAGGTTAATAAATGA[C/T]ACATTGTCTTTGATT | 57626 |
rs73520084 | snp | C/G | 0.122758 | 0.215196 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707371 | ATTCAGATTCTGTTT[C/G]TTGTTGTGGAAAATG | 57626 |
rs73520088 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710686 | GAAATAAGCAATCTA[C/T]AGATGTATAAGCATT | 57626 |
rs73522005 | snp | G/T | 0.081446 | 0.184634 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716780 | TCTTTCTTCTAATAC[G/T]GTAAGCTCTGTATAG | 57626 |
rs73522016 | snp | A/G/T | 0.070071 | 0.173687 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720411 | TTTTGAATGGTTAGG[A/G/T]TGTGTCACACATTGT | 57626 |
rs73522021 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722120 | ACCTAGCACAGCTCT[C/T]GTACATAGTTTATAA | 57626 |
rs73522030 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723274 | ACATTAGAGTGACTA[C/T]GACTAACAATAATGC | 57626 |
rs73522051 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725446 | ACTTCTCACATCTCA[C/T]AGGTCAGAACCAGAC | 57626 |
rs73522054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726733 | ATTCACCAACCCAAA[A/G]CTGTCAGTTCAACCT | 57626 |
rs73522070 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742556 | TGAATTAGGCAAAGT[C/T]TCTGCCCACAGTGAG | 57626 |
rs74089054 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040184 | TATTTAAGTAAACTC[A/G]AGGGTCAATGGAATG | 57626 |
rs74089055 | snp | C/T | 0.116138 | 0.211142 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042040 | GTTAGACTTTCTCAT[C/T]TCTAGTCTTGGTCTA | 57626 |
rs74090420 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724752 | AAATCACATGATCAT[A/C]TCAATAGATGCAGAA | 57626 |
rs74090425 | snp | A/C | 0.155987 | 0.23165 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726784 | TGCTCCAACTCTACG[A/C]GTTTTATAATCCTGC | 57626 |
rs74090427 | snp | C/T | 0.209693 | 0.246729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731689 | AGTAGCTATTTGCTT[C/T]AGCTTTTTGTGATTC | 57626 |
rs74090428 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731706 | GCTTTTTGTGATTCT[A/G]GTTCACCTTTTCTTT | 57626 |
rs74090429 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732156 | ATCATAAACAAATTG[A/G]CATTGATTGAATTCA | 57626 |
rs74090430 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733600 | AATGACTAATACATA[C/T]ATTAAAGATGTTTGA | 57626 |
rs74090431 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733673 | ATGGATAAAGATAAA[C/T]AAAAGACAAGTCGGA | 57626 |
rs74090432 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733686 | AATAAAAGACAAGTC[A/G]GATGTTACCAAGTCA | 57626 |
rs74090435 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737841 | TAAGGGCAGCCCAGA[C/T]GAGGGGGATTTTCCC | 57626 |
rs74090437 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738089 | TGGTATCTCCAGGGG[C/T]GGGACGGACCCAGGC | 57626 |
rs74090438 | snp | A/T | 0.081446 | 0.184634 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740677 | AAAATGAAAAAAAAT[A/T]AAAAATTGAATAGAT | 57626 |
rs74090440 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744094 | TATGGCTTTTAAAGT[C/T]GTAGTCCTAGATATA | 57626 |
rs74090441 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744665 | AAAGGTACACCCCCC[C/G]CAAAAGCTAACCGTA | 57626 |
rs74090442 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744825 | AACATTTTTAAATTG[C/T]AAATATTATTACAGT | 57626 |
rs74090443 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749697 | AAGGAATTGAAGAAG[A/T]TAATCTGTCTATACA | 57626 |
rs74090445 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759116 | AGGCAAATCTGGGCC[A/G]AGGAAGATGGGTCTA | 57626 |
rs74090448 | snp | G/T | 0.0644693 | 0.167566 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768234 | TTTGTAAAACTTGCA[G/T]TTTTTCTAGATTGTA | 57626 |
rs74090449 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769557 | AGAACATCTATTCCT[A/G]TTTGCCACTCTTTCC | 57626 |
rs74090457 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800858 | ATATTTATCATAATA[C/T]AGATTACAAACAGAA | 57626 |
rs74090462 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805327 | ATAAATTTTGAAAAT[C/G]CAGCATTTTGCTTGC | 57626 |
rs74090466 | snp | C/T | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817981 | GGAAATATTTGACCC[C/T]TAAGTTTTACTCTGA | 57626 |
rs74090468 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819095 | TAAAAGGCTGTTCTT[C/T]AAAAGATCCTGATAG | 57626 |
rs74090469 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820546 | GAATTGGCCAACAGA[A/G]GCATAAGCGTAATAT | 57626 |
rs74090470 | snp | C/T | 0.174932 | 0.238463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822375 | AAAATTAATAATTTC[C/T]AATTATTGAAACAAA | 57626 |
rs74090471 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822450 | AGCATTATCAGAAAG[C/T]GACATTGTCTATTAA | 57626 |
rs74090472 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822523 | ATTAGTCAGACTTCC[A/G]AATACATGAAGTCAT | 57626 |
rs74090477 | snp | C/T | 0.142272 | 0.225598 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834994 | TTTGCATTTTAGAGA[C/T]GTAGAAGTTATAACT | 57626 |
rs74090478 | snp | A/T | 0.168135 | 0.236216 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835056 | AAAATTAATTAACTA[A/T]GAAAATGTCAATGAG | 57626 |
rs74090480 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835141 | GTTATAGACAAAATA[A/C]CTACATTTCAAAAAT | 57626 |
rs74090481 | snp | C/T | 0.16846 | 0.236329 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835220 | AAAAGAGAAAAAGGA[C/T]ACTTCTGACTGTTGG | 57626 |
rs74090482 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835306 | CAAATTACAAAAAAA[A/T]TTATTTGCATTGCTC | 57626 |
rs74090483 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835849 | AGTGAAGAACATTAA[A/C]ATTCATAAATAAATA | 57626 |
rs74090484 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835930 | TACAAATACACAGGG[G/T]CTTCTTTTAAACATG | 57626 |
rs74090485 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836918 | TTATTATATATGTGA[A/T]TAAATACATAAAAAA | 57626 |
rs74090486 | snp | C/T | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837141 | ATTCTTATATATTTT[C/T]GAAAAAGAAATTAGC | 57626 |
rs74090487 | snp | C/T | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837345 | AAGTAAACTGTGACA[C/T]TTCTGTGTGAATAAT | 57626 |
rs74090488 | snp | C/T | 0.149999 | 0.229128 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837433 | CAATGTAAGTAATGA[C/T]TACAAGCAACAAAAG | 57626 |
rs74090489 | snp | A/T | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837823 | TTCTAAGGCTTTCCT[A/T]CTTCAATAATAGTAT | 57626 |
rs74090492 | snp | A/G | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837837 | TTCTTCAATAATAGT[A/G]TATTCTAAGCTTTAG | 57626 |
rs74090493 | snp | A/G | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838004 | TTCATATTTACAGGA[A/G]TTGCTCTTTTCCAAA | 57626 |
rs74090499 | snp | A/T | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839402 | ACCACACAGAGTAAA[A/T]AAAACACTTATAGTG | 57626 |
rs74090500 | snp | C/T | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839509 | ATGTCAGGTGAAAGA[C/T]ATTTAATTTATTGAA | 57626 |
rs74090605 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932654 | ATTTAACCTACTGTA[C/T]CTAAGATATTTTTAA | 57626 |
rs74090609 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934999 | ATATATGTATATATA[C/T]ACATATTATCATTAT | 57626 |
rs74090610 | snp | A/C | 0.079617 | 0.182947 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935223 | ACTGGTGAACTTGGT[A/C]CATAGTTCACCCACT | 57626 |
rs74090611 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935279 | ACTGGTGAACTTGGT[A/C]CATAGCAGTCAATAG | 57626 |
rs74090620 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937663 | CCTGATGCTGAGCTC[A/G]CAATCAAAATTCTCC | 57626 |
rs74090622 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939852 | AAAGAACAATAAATC[C/T]AGTATAGAATGTGTT | 57626 |
rs74090626 | snp | A/G | 0.313326 | 0.241847 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944710 | TGTGAAAATTGCAAA[A/G]CTGATTATAAAATTC | 57626 |
rs74090627 | snp | C/T | 0.32627 | 0.238082 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944763 | ATAATCCAAACAATT[C/T]TGAAAAATAACAAAG | 57626 |
rs74090631 | snp | A/G | 0.313082 | 0.241911 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946068 | ATTAGGCTGAGTGAA[A/G]GAAACCAGACAGAAA | 57626 |
rs74090639 | snp | A/G | 0.326741 | 0.23793 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949469 | AGAAACATTATCAAC[A/G]TGACTTATCACTGGT | 57626 |
rs74090641 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949644 | ATCTCCATGACGGTG[A/G]AATAACTGGCATAAA | 57626 |
rs74090642 | snp | A/G | 0.313326 | 0.241847 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949760 | GGATTTTTTGAATAA[A/G]TGTTTCAAAAAAGGA | 57626 |
rs74090650 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954052 | AAGTTAAGTAATTTG[A/G]CCAAGATCCATAACT | 57626 |
rs74090659 | snp | C/T | 0.118584 | 0.212673 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962900 | GTGTAAAACCATTTA[C/T]ATTCGGCTATTTTGA | 57626 |
rs74090665 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965189 | TTGCAGATACTGCAG[A/T]TTTTTAAAAATAATT | 57626 |
rs74090679 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970543 | TTTTTTCAGGAACTG[G/T]ACTTGGCCTAACAGG | 57626 |
rs74090680 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970924 | ATCCTTTATGTTCAT[A/G]TAGTCTTCATTTCAT | 57626 |
rs74090681 | snp | C/T | 0.039522 | 0.134904 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973219 | AATTGATAATTGTGA[C/T]CAATATCAAGTTAAA | 57626 |
rs74090683 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973284 | ATATTATGTAGAGTC[A/C]TTCAATGAGGGCAAT | 57626 |
rs74090689 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978117 | TGTATTTTAAGAATT[C/T]GGGCTCAAGCACATA | 57626 |
rs74092313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993199 | CCAATGAATGAGATA[C/T]AGGGTTTATCAAGGG | 57626 |
rs74092317 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994290 | GCTCTGAGACTTGGA[A/G]ACAATTAGAGGGCAT | 57626 |
rs74092318 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995017 | CCAAAGACAGTGTGG[A/G]CACGAGTGTCACTAT | 57626 |
rs74092320 | snp | C/T | 0.315273 | 0.241329 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998205 | GAGAAGCCTCTGCTT[C/T]AGGTCTGAGATTTTG | 57626 |
rs74092329 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011035 | GAGTAATAAATTCAA[C/G]TTTCATAATTGTTAT | 57626 |
rs74092334 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015996 | TTATTTAGAGATCAA[A/G]AAAAATAATGTATAG | 57626 |
rs74092453 | snp | C/G | 0.178144 | 0.239451 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701172 | TAATTGTTCTCATAG[C/G]TTAGGAAAATGAGGC | 57626 |
rs74092454 | snp | A/G | 0.0298908 | 0.118541 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701525 | CTGTATAAGTTTAAT[A/G]TTTTCTTGTTTCCTA | 57626 |
rs74092456 | snp | A/G | 0.223225 | 0.248562 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703188 | ATGGTGGTCCCATAA[A/G]ATTATAATGGAGCTG | 57626 |
rs74092457 | snp | C/T | 0.178465 | 0.239547 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705516 | AGTCCACTTACAGGA[C/T]ATATGGAGTGAAAGT | 57626 |
rs74092459 | snp | C/T | 0.228253 | 0.249052 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705610 | GGATTTTGTGTGGGT[C/T]GGCTGCTCATCCCTT | 57626 |
rs74092460 | snp | A/G | 0.183886 | 0.241099 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707387 | TTGTTGTGGAAAATG[A/G]AAATCTTATTAAGTA | 57626 |
rs74092464 | snp | C/T | 0.168785 | 0.236441 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711061 | CTTTGTAAAACCAAA[C/T]TGAATTTTTTAAGAA | 57626 |
rs74092604 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842962 | ATATCACATGTTCTC[A/G]CTTTTATGTGGGAGT | 57626 |
rs74092607 | snp | A/G | 0.031825 | 0.122064 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846323 | AATAATAACTGATGC[A/G]TTATAGGGTAACCCA | 57626 |
rs74092613 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850867 | TACATTATCCTTCAC[A/G]AGAACAATTTTCGCA | 57626 |
rs74092617 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856133 | GAATACTGTGCAACT[C/T]TGGAAGCTAGAGATA | 57626 |
rs74092619 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858978 | TATCTTGATTCACCT[A/G]TTCATATACGTGTCC | 57626 |
rs74092621 | snp | C/T | 0.212122 | 0.247114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866414 | TTTAGGATCATTTAC[C/T]CTAAATGAAAACCCA | 57626 |
rs74092622 | snp | A/G | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867404 | ATATTTGTTTCAGTT[A/G]CTGCAGCTCTTTTGT | 57626 |
rs74092626 | snp | C/T | 0.162909 | 0.23434 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870381 | GAGGGATCTACCCCA[C/T]GACCCAAACACTTCC | 57626 |
rs74092640 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870632 | TGATCCTACAAAATA[A/G]AAATATATATATATT | 57626 |
rs74092643 | snp | A/C | 0.153 | 0.230415 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889066 | TATATATATAATTTT[A/C]TATTGCTTTTTAGAA | 57626 |
rs74092661 | snp | C/T | 0.104149 | 0.203046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923232 | GATATAGTTCATTAA[C/T]GTTAAATACTGATGA | 57626 |
rs74092663 | snp | A/C | 0.0785177 | 0.181917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923465 | AAGCACAGAATACTA[A/C]AGAGTGTCTATTACA | 57626 |
rs74092664 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924109 | CTGGACCTTGGGCAC[C/T]GATAAGCATGGGAGG | 57626 |
rs74092665 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924555 | TCTGAGCTGTTCTAT[A/C]ACTTAATAAAACTCC | 57626 |
rs74093205 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045574 | TATTTAAAAAACACA[A/C]AACACACACACACAC | 57626 |
rs74093208 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045575 | ATTTAAAAAACACAC[A/C]ACACACACACACACA | 57626 |
rs74093212 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053526 | AAATTAATTATAATA[C/T]TCTTATGGAAGTCTA | 57626 |
rs74093213 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054027 | CTCTCATTTCTGGGA[A/G]AAATGTGAGTATTAA | 57626 |
rs74093233 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068636 | ATTTTGTGAGTGGAA[A/G]TAGAGCTGTTTCTGT | 57626 |
rs74093242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086176 | AGAAAGAACAACATG[A/G]AGTGTCAGGAAGCCA | 57626 |
rs74093244 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092548 | AGCTTTTATATTATT[A/C]GATACAAAGTTTAAT | 57626 |
rs74093245 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095362 | ATTGACTACATAATT[A/G]TGGAACCTATTGGAA | 57626 |
rs74093253 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106597 | ACAGTTTAACTCAAA[C/G]ACTTACTCTGAACAA | 57626 |
rs74323565 | snp | A/C | 0.46875 | 0.121031 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855698 | GCCTCAGGAAACTTA[A/C]AATCATGGTGGAAGA | 57626 |
rs74328077 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834328 | TGTATTTATGTCATT[G/T]ATGTATTATCTATTA | 57626 |
rs74333241 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014872 | TTCCCCTTTAGTTGG[A/T]GTAGGTATCTAGAAG | 57626 |
rs74343642 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946706 | TTTGTAGCAATTAGG[G/T]GTTGCTATGTTGCCC | 57626 |
rs74348796 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718921 | TGATAATTCACCTTT[A/G]AGAGTTTGAAAGGGT | 57626 |
rs74368919 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091264 | GTCAATGTCTTCTTT[C/T]TCTATCTTGAACCCT | 57626 |
rs74369634 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034691 | AGGTGCATGTGTATT[G/T]TGAGGAAGAGGGAAA | 57626 |
rs74374792 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731926 | GTTTTTCCATCATAT[A/T]AAAATATTTTATTTT | 57626 |
rs74378812 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759003 | GTCCCAAGAGCTTAC[A/G]TGGCACCCATGGATG | 57626 |
rs74385938 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032193 | ATAGATGCTATGACT[A/G]TGGAGTGGTGAAGTG | 57626 |
rs74388388 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948118 | AATGAAATGTTTATA[A/C]TCTCTCTTAGCAAGT | 57626 |
rs74396935 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814611 | CAATAGAAACATACA[C/T]GTGACCAAGAAACAT | 57626 |
rs74402306 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820024 | AGAAGAGAGCAGTCC[C/T]TCTAAGAATCTTGAT | 57626 |
rs74408932 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828425 | TCTAACTTTATCTCA[C/T]AGGGGTTCTTGGGGA | 57626 |
rs74416020 | snp | A/G | 0.122064 | 0.214785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868684 | CTTATATTTCAACAC[A/G]TGTTAAATGTTAGGA | 57626 |
rs74422427 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807138 | AGAGAAACCATGTCA[A/T]CCCATGCATATCTAG | 57626 |
rs74422537 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795031 | ATTGTATTTGAGTAC[G/T]ATACATAATGCCGAA | 57626 |
rs74430269 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881139 | GCTCACATAATTTGA[A/G]TTCCATAAATTATTT | 57626 |
rs74432327 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774231 | ATATACAAACTCACA[A/G]ATACAAATAGAGTTC | 57626 |
rs74434938 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016005 | GATCAAGAAAAATAA[C/T]GTATAGAAAGATTAA | 57626 |
rs74441951 | snp | A/G | 0.164219 | 0.234823 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709731 | TTCAGAAATTTCTCT[A/G]CAAAACTTTAGGGAA | 57626 |
rs74445435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864757 | AATGTATGCCAAATA[C/T]TGGAGATGAAAATCT | 57626 |
rs74448656 | in-del | -/TATAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855866 | TGTTATATAATATAT[-/TATAT]ATTATATATGTTATA | 57626 |
rs74464879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016672 | TGCAGGTGCCCCTCC[A/G]CACAAACAGCTTGGG | 57626 |
rs74467349 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774663 | CTTGCCTTCACTTAA[A/T]AAAAAAAAACACACA | 57626 |
rs74477296 | snp | C/G | 0.151001 | 0.229563 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723000 | ATTCAGCCATAAAAA[C/G]AATAAACTCCTAATA | 57626 |
rs74484999 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901774 | CAATGAGTTTTTCAT[A/T]TTCTTTCTTTTTCTT | 57626 |
rs74501376 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016625 | GCACCGATGAGGATC[A/G]AAGGGAGGCTGAGAG | 57626 |
rs74506710 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717345 | TTATTGAGGAGTTAC[A/G]TGTGAAATCATCAAT | 57626 |
rs74516971 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096604 | TTTATTTTTTCCTAT[C/T]GAGTTCTTTGAGCTT | 57626 |
rs74520248 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065334 | CTATAACAGATGACA[A/G]TGGCATCATAGCCAA | 57626 |
rs74544784 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868432 | ATTTTTTTAGATGAT[A/G]GTGATAATGAATGTT | 57626 |
rs74549278 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989393 | GTCAGGAGTCAGGCA[A/G]TATGACTCCTCTAGA | 57626 |
rs74549284 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086606 | AAAGAAAGAAAGAAA[A/G]AAAGAAAGAAAGAAA | 57626 |
rs74562861 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715525 | GCAGTTTTATTATTT[A/T]TTTTTTTTTTTTTGA | 57626 |
rs74569189 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932877 | AGGGATCTAATTTAC[A/G]TAATGGGTAGCAATT | 57626 |
rs74569481 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746981 | GTAGCCAGCCCTAGC[C/T]GCCAGATTTCACTTT | 57626 |
rs74573917 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876551 | ATTAGATTAAACCAT[A/G]TTCCTCTAAATCTAG | 57626 |
rs74584428 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965625 | AATGATTAAGTTTAG[C/T]GAGGGAGACATGTAG | 57626 |
rs74586978 | snp | A/C/T | 0.0256215 | 0.110247 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726268 | TTGCACAATAAAAGG[A/C/T]TTAGAATCCCTCAAC | 57626 |
rs74591187 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883705 | AATTGATAATCTCTG[C/T]AGAGAAAAACAAAAT | 57626 |
rs74591702 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873275 | TATTTATGCCTTTAG[C/T]GGACATAAATAATTT | 57626 |
rs74593962 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966946 | AATGACATGATTTCA[A/T]TTTTTTAATGGCTGA | 57626 |
rs74596177 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050326 | CAGAAGAAGCTTCTA[A/C]CTTTGTATTAAACAT | 57626 |
rs74601771 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960360 | GAACCTGCCTTTCTT[C/T]GTCTCACACCAGTAT | 57626 |
rs74603966 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948883 | ACTGCCTATAAAATT[A/C]ACAACGTAAATCAAA | 57626 |
rs74628075 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738550 | CAATTTAGAGAGGAA[C/G]ATAAATTACCTGATA | 57626 |
rs74633158 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947979 | AAGGGAAAACCTACA[C/T]GTTTTTAGTTAGATG | 57626 |
rs74638111 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768542 | TAAAGATGTGGAAAG[C/G]GTTGTACAATAGTTT | 57626 |
rs74645440 | snp | A/T | 0.0360663 | 0.129354 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722921 | ACGGAATCAACTAAA[A/T]GCTCAACAATGGATA | 57626 |
rs74657546 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715524 | GGCAGTTTTATTATT[A/T]ATTTTTTTTTTTTTG | 57626 |
rs74694217 | snp | A/C | 0.396727 | 0.202413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745301 | TTTTTAATTGGATGT[A/C]TCTTATTATTAATTA | 57626 |
rs74699234 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985487 | TCAAAAAGAAAAAAA[C/T]ATATAAAAAATACTG | 57626 |
rs74705161 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949848 | ATGACATTTAAATTT[C/T]ACTGCAATTTAGAAT | 57626 |
rs74705681 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69813819 | TAGATTGCCTTGGTC[A/G]GTATGGTCATTTTGA | 57626 |
rs74710376 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818546 | TTAATTCTAAAGATG[A/G]ATGCAAATGCAGATA | 57626 |
rs74725148 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035008 | CAAATATTAATATTT[G/T]TGGTACTTATAGAAT | 57626 |
rs74726198 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764147 | TCCGTGCATATTTTA[A/G]GTTTGCCCTAAAGAT | 57626 |
rs74728370 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979465 | GATAATATTTATTAT[C/T]TAACCTTCTTCCCAT | 57626 |
rs74733220 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716618 | TCTTTCACCAGCCCT[C/T]ATTACTGGGATGCAG | 57626 |
rs74733744 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735265 | GTATCTCAAATAACA[A/G]CTGATATCAGAGACT | 57626 |
rs74737459 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712782 | TTTTTTGGGGGGGGG[G/T]TTTTGTTTGTTTGCT | 57626 |
rs74741795 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002428 | AAGGGAGAAAAAAAA[A/T]TTTTTTAAATGAACG | 57626 |
rs74750706 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833812 | TTCTATATATATATA[C/T]ACACACACACACATG | 57626 |
rs74759894 | in-del | -/TTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715536 | ATTTATTTTTTTTTT[-/TTT]GAGACGGAATCTCGC | 57626 |
rs74764726 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991914 | TTACCCACTTCTGCA[C/T]AAAATGTACTTTCCA | 57626 |
rs74787215 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064801 | CAGGGTGAGAGAAAC[C/T]GAATACTAGAAAATA | 57626 |
rs74787548 | snp | A/T | 0.107341 | 0.205301 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985492 | AAGAAAAAAATATAT[A/T]AAAAATACTGGTGAG | 57626 |
rs74791248 | snp | C/T | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010066 | GAGAATTCTTGGTAG[C/T]TTCAAAACAAGGAAA | 57626 |
rs74792828 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885435 | TGTTATTTTTTTTTT[C/T]TCTTTACACTTCATT | 57626 |
rs74799982 | snp | C/T | 0.130694 | 0.219696 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919167 | CTTTAATATTATACT[C/T]AATAAAAAGAAACAT | 57626 |
rs74806473 | snp | A/G | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842612 | ACTAGTAAAGCCACT[A/G]TGGAAAACAATGTGG | 57626 |
rs74815109 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055414 | GTCCTACAAGAAATG[C/T]TAAAAGGAGTTCTTC | 57626 |
rs74817010 | snp | C/T | 0.356811 | 0.226034 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744731 | CCTGATTTGAACTTA[C/T]AAATTAAGTAATATA | 57626 |
rs74817564 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018060 | CTAGCGCAAAAAAAA[G/T]TTGAAAATTTATCTT | 57626 |
rs74836317 | snp | C/G | 0.476314 | 0.106217 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811838 | ATCAGTTTTGTTGAT[C/G]TTTTCAAAAAACCAG | 57626 |
rs74845712 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080959 | TAGCAGCTTAAATTC[C/T]TTTAAATCCAGCTTG | 57626 |
rs74866647 | snp | A/G | 0.103082 | 0.202275 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846330 | ACTGATGCGTTATAG[A/G]GTAACCCAGTAGCTT | 57626 |
rs74868348 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69822572 | CATCAGAGTTGGGCA[A/T]TGCAATGGTCTCCAG | 57626 |
rs74872690 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038789 | AGAGACAGGGTTTCA[C/T]CACGTTGGCCAGGCT | 57626 |
rs74880030 | snp | G/T | 0.0803491 | 0.183626 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859254 | CCTCCTCATCCATTT[G/T]GCACTTTTTTTTTTT | 57626 |
rs74884727 | snp | C/T | 0.089084 | 0.191327 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859478 | CGAGCTCCAGTAGGG[C/T]AGACGCTGTGACAGC | 57626 |
rs74884874 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871545 | CTCTGTTTCCCTTTT[A/T]ACTATAAATTCCACC | 57626 |
rs74888168 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789999 | TTTGTCCTCACCAGG[C/T]GTTCACCGAGATGTA | 57626 |
rs74892336 | snp | C/T | 0.077417 | 0.180873 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053108 | GGAAAAATGAAAAAG[C/T]GATGTGTAAATGGTG | 57626 |
rs74899361 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940496 | GTCAGCAGAAATGAT[A/G]GTTCTTCCTTTGATT | 57626 |
rs74905296 | snp | C/T | 0.212122 | 0.247114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855839 | AAAATATTATATATA[C/T]GGTATTATATATGTT | 57626 |
rs74905912 | snp | A/G | 0.16911 | 0.236552 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026720 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 57626 |
rs74922877 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795881 | AAACGTTTATTGTCC[G/T]CTTCCCCACAGATTT | 57626 |
rs74938483 | snp | G/T | 0.104859 | 0.203554 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009868 | TGGGTTCAAAAAAAG[G/T]TCAGAAAAAAAACCA | 57626 |
rs74944805 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984155 | GTACAAATAGACAAG[C/T]GGGAATGGTATAGGA | 57626 |
rs74949500 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013151 | ATTTAGAAGGAAATG[A/C]ATAGAAACTCACATG | 57626 |
rs74960863 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735953 | AATATGTATTCATTG[G/T]ATATGTGTATCTGTG | 57626 |
rs74971568 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974811 | ACACATATTATGACA[G/T]TGAATAATTCTCTCA | 57626 |
rs74986263 | snp | A/C | 0.046775 | 0.145601 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814075 | GGAAAAGAATAGAGA[A/C]CCCTGAAATAAAACC | 57626 |
rs74987709 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828405 | CAGTACCCAGAGAAA[A/C]CATTTCTAACTTTAT | 57626 |
rs74996459 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776821 | AAATTAATATTTTTT[C/T]CTCTTCTCTTAACAG | 57626 |
rs74997244 | snp | A/G | 0.368324 | 0.220226 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758981 | TGTTCCCCCCAGGGT[A/G]TTCTGGGTCCCAAGA | 57626 |
rs75018918 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911570 | GGAATATCATCAAGA[A/G]AAAAAAAAAAAAAGC | 57626 |
rs75032011 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052757 | CATGCACATACATAG[A/G]CCTTAGGTTAATTTC | 57626 |
rs75036119 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871302 | TCTGAGCCTGTCCCC[C/T]AAAACCATTCTGTCA | 57626 |
rs75050069 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872062 | AAAGGACTACCTGAG[A/G]CTAGATAATTTATAA | 57626 |
rs75065371 | snp | A/C | 0.0584853 | 0.160693 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815138 | GTCCTTACAGAAAGC[A/C]GTTATTAGATTTCTC | 57626 |
rs75069642 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020990 | ACATCCCCCACCAGA[C/G]TGATACATTCACTAT | 57626 |
rs75072001 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856768 | ATGATAATTAATTAA[C/T]TCCAGGAAAATGCTA | 57626 |
rs75081775 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826542 | CCAAGATCCTGCCGT[C/T]GCACTCCAGCCTAGG | 57626 |
rs75082647 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993474 | TTTAGTTCAGGACTC[C/T]AAACACACTTTTGAA | 57626 |
rs75084747 | snp | C/T | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842147 | TAAGCAAAGGATTTA[C/T]GACTAAGACATCAAA | 57626 |
rs75104622 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70003423 | TGACATGTTAAATAC[A/C]TTCAATTGATATTTT | 57626 |
rs75105467 | snp | A/G | 0.151334 | 0.229706 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757736 | GCCAGAGGATCACCT[A/G]AGGTCAGGAGTTTAA | 57626 |
rs75106411 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980979 | TCCATACACCACACA[A/G]ATGTGTTGCTCAGAA | 57626 |
rs75108220 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727181 | ATATAAATAATCTTA[G/T]TTTGGTTTTAAGCAA | 57626 |
rs75116532 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736991 | TCAATTGAGGTACCA[A/G]TTTTCTCTTATTAGG | 57626 |
rs75118882 | snp | C/T | 0.151001 | 0.229563 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719969 | AAAGGCATTATCCTA[C/T]TTGTTGATAAGCAAG | 57626 |
rs75119086 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69803845 | CAGTACCTCAGTTCT[A/T]CAACCACAAGGAATA | 57626 |
rs75127872 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725488 | CCTAGTTAGTAAGAT[G/T]CTGGAAAGTCTTGTC | 57626 |
rs75147182 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831683 | TCCCTAATACACATA[C/T]ATGCAAAAATCCTCC | 57626 |
rs75159592 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754325 | TGTTAAAAATGTAAA[A/G]TCCCAAATACATGAA | 57626 |
rs75161577 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967328 | TAGTTTGGAAAAAGA[A/G]AAGATTCCAACCCTC | 57626 |
rs75165195 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798763 | CATGAATGCATAACT[A/G]AAAATTAAGAGTTAT | 57626 |
rs75177281 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054377 | ACTATTATGTTTCTA[G/T]AGGTTTTTTATGTCT | 57626 |
rs75177733 | snp | A/G | 0.132409 | 0.220618 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897622 | CTTCCTCCAGAGTGC[A/G]TTGACTACCTAAAGA | 57626 |
rs75178116 | snp | G/T | 0.0872718 | 0.189788 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736206 | GAAAGAAACAAACAA[G/T]CCCATTAAAAATTGG | 57626 |
rs75195967 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032464 | TGAGTATAGTGGATC[C/T]CAATATCATAAAAAA | 57626 |
rs75234827 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824686 | TTTATGTGAAGTCTA[C/G]AAATAGGCAAAACTA | 57626 |
rs75260092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836215 | CTGGGCAGTCTGATG[A/G]GGCTGAAAAGACACA | 57626 |
rs75266678 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032263 | ATTGTTGTGACAATG[C/T]GCAAAACACAAAATC | 57626 |
rs75270827 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785182 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCCAGAAT | 57626 |
rs75274319 | snp | A/T | 0.0962929 | 0.197165 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938274 | ATACCAGAGCATCAC[A/T]TTTTCAAAATAATTT | 57626 |
rs75278739 | snp | A/T | 0.0941369 | 0.195465 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951325 | TTATTTTTTCTTTCC[A/T]TTATATTCTACATCA | 57626 |
rs75293487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956898 | GCATAGAAAACGTTC[A/G]TCTGTAAAATGTATA | 57626 |
rs75294506 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69754007 | ATGCCTGGCTAATTT[C/T]TTTTTTTGTTTTTAG | 57626 |
rs75299323 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793828 | CCTGACATCATTTGT[A/G]ACGTTCTGAGTGAGA | 57626 |
rs75301731 | in-del | -/GTGTGTGTGTGTGTGAGAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719196 | TACGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGAGAG]AGAGAGAGAGAGAGA | 57626 |
rs75307646 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794860 | AGTTACCTCTCAGGA[A/C]AGGATAAAGACAAAA | 57626 |
rs75324414 | snp | C/G | 0.264358 | 0.249587 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988092 | ATAGCTTTTTTTTGG[C/G]GGGGGGAACCTCTCC | 57626 |
rs75325380 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055023 | TATTCAAAGACGTAA[C/T]AGAAATCTTTCCAAA | 57626 |
rs75332247 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719766 | GAAATTTCTATTTTT[A/G]TATAGAAATTGCAGT | 57626 |
rs75346116 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794511 | AGGAAAGAAACAGTA[A/G]AAAAAAAAAGAGGAG | 57626 |
rs75355493 | snp | A/C | 0.0569829 | 0.158885 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066361 | TGAATACCTACTATA[A/C]GCTGAGAGCTATGTG | 57626 |
rs75355572 | snp | G/T | 0.0953825 | 0.198352 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842371 | TAATCCCATTAAAAA[G/T]TGGGCGAAGGACATG | 57626 |
rs75368703 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768870 | AAGTGTGGTTCTTAT[C/G]TTTACATGGAACTAA | 57626 |
rs75388120 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868635 | CTGTTCAATATCTGC[G/T]TTGTTATTTATTTTG | 57626 |
rs75389334 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69708446 | GATTCCCTGGGTAGG[A/T]AGGTACTTTCAGTTT | 57626 |
rs75389943 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096783 | GTTTCCAGATAGTCT[C/T]AAAGGAGAGAAATCA | 57626 |
rs75409424 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720808 | TGGGGCAGAGGCTGA[A/G]GTGAGAGTGGTGGTT | 57626 |
rs75413404 | in-del | -/GCA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69717763 | GTCAGTCTATTAGCA[-/GCA]TTTTTAAAATAAATG | 57626 |
rs75433930 | snp | A/C | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809248 | TAAGTCCCAAGGCAC[A/C]CAGTCATCAGACTAT | 57626 |
rs75442762 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045673 | TGCTGGCTTTATTCT[G/T]ATAAACACATATGGA | 57626 |
rs75446110 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939903 | TTATGGTACGCTATA[G/T]TTCATAACAAAAAAA | 57626 |
rs75453304 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032652 | TTTTTTAAATGTATA[G/T]TTTTGAAAAATTCTT | 57626 |
rs75459199 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989390 | GAAGTCAGGAGTCAG[C/G]CAGTATGACTCCTCT | 57626 |
rs75465558 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893952 | ACATCACTCTCCAAA[A/G]GACACATAGGATGTT | 57626 |
rs75469025 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899095 | CACAAGCCAAACTCA[A/G]GAAGGTTGTAAGGAG | 57626 |
rs75513278 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948756 | ACACATCATCCCCTA[C/T]TAACAAATGCACAGA | 57626 |
rs75520900 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089842 | TCTACTTCCTACTTA[C/T]AGCTAAGACAGCACT | 57626 |
rs75523671 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093372 | TGGGGCATCTCTGAA[A/G]TACTTTTAGGTAACC | 57626 |
rs75526364 | snp | A/G | 0.046775 | 0.145601 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709484 | ATGCGAGTTAGAAAT[A/G]TAACAAAATATAGTG | 57626 |
rs75560943 | snp | A/C | 0.199254 | 0.244796 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100471 | ATTTCTTCATTTTTA[A/C]AGATATGACAAACTT | 57626 |
rs75565434 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064802 | AGGGTGAGAGAAACT[A/G]AATACTAGAAAATAT | 57626 |
rs75566519 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916760 | ATAATAAAATAAAGT[A/G]AAAAAAAAACCACAT | 57626 |
rs75569924 | snp | G/T | 0.00150008 | 0.0273457 | synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107328 | CACCTCCTCCTCTAG[G/T]GACTCCACGTAGAAG | 57626 |
rs75572078 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946939 | TCAATGGGAAAATTG[A/C]AATTACTTTTGTACC | 57626 |
rs75573984 | snp | A/C | 0.0901694 | 0.192235 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737109 | AGCTTCCTTTCCTAG[A/C]CAAAGAAGGCAGTGA | 57626 |
rs75574298 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849729 | CTTGCAGAAAATCAG[A/G]AAAAAAAATCTGCTA | 57626 |
rs75605606 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762968 | CAGAAGCAGAACATT[C/T]GTCCACTCCTCTTAA | 57626 |
rs75609568 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057089 | AAATAAATAAAATTA[C/G]AGATAAAAAAACATT | 57626 |
rs75613531 | snp | A/G | 0.315758 | 0.241197 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070459 | TGGAGTAAAATATTC[A/G]AAATGTTAAAAGACA | 57626 |
rs75635812 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051149 | ACAAAATATTCATTA[A/C]GAAATGTTTTCACAC | 57626 |
rs75639940 | snp | A/G | 0.411914 | 0.190483 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011809 | TTGAATTAAATTTGG[A/G]GGTTCCGTATTTGTC | 57626 |
rs75663319 | snp | C/T | 0.116838 | 0.211584 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713970 | TCTCCTCAATATATT[C/T]AGGGTGTTTCAGGCT | 57626 |
rs75670552 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926563 | TGCCTATCAAAATCC[C/T]AGCTGGCTATTTGCA | 57626 |
rs75695632 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781457 | AAACCTTTGCCTGTC[A/G]GAAGTTTGAAGCATG | 57626 |
rs75710339 | snp | A/G | 0.104149 | 0.203046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774997 | GGGAAATGCTTTTTG[A/G]AACAAACTTTAATCT | 57626 |
rs75720382 | snp | C/T | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714955 | GCATATTTGTATTTC[C/T]ACAGAATCCTTCTTC | 57626 |
rs75720863 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041719 | GGAGTGGGGTAGAAA[C/T]GCCTTGTCACTCCTT | 57626 |
rs75730203 | in-del | -/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69712771 | TTTTGTTTTTTTTTT[-/TT]GGGGGGGGGGTTTTG | 57626 |
rs75749044 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852514 | TATTTCAATTATCTT[C/T]AACTAAAACCTTTTA | 57626 |
rs75752906 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074733 | AGTGAAACTTTAACC[C/G]GAGCAAGCAAGAAAA | 57626 |
rs75763678 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789921 | AGAGCTACCTAATAC[A/G]TCTAGAGTAGGTAGA | 57626 |
rs75764668 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856696 | CATAATAAATACTTA[C/G]TGCATATTTCCCTAA | 57626 |
rs75768935 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763562 | TAAATGTGTGATCAC[A/G]AGGACACTTTAACCT | 57626 |
rs75782819 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738403 | GGAGGCTGAAATGGA[C/T]GAATTGAGAGAAGCA | 57626 |
rs75795000 | snp | A/T | 0.0327778 | 0.123752 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937461 | ATTCTTGTTATTCTA[A/T]TCTGTTTCCGTTTGC | 57626 |
rs75808613 | snp | A/G | 0.313082 | 0.241911 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945269 | TGAGCCACTGCACCC[A/G]GCAGCTATAAAACTT | 57626 |
rs75812539 | snp | C/G | 0.140581 | 0.224783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792023 | TGCTGGGCTTAATAC[C/G]TAGGCGATGGGTTGA | 57626 |
rs75813804 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855840 | AAATATTATATATAC[A/G]GTATTATATATGTTA | 57626 |
rs75833012 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963961 | TTATTTACACATGAC[A/G]TAGAATTCTAGGGTG | 57626 |
rs75834567 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727391 | GAAACTAAGTGGACA[C/G]TGAATAGTGGACAGT | 57626 |
rs75836128 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712536 | TCTATTCCATTTGTC[C/T]ATTTATTTATAGTGT | 57626 |
rs75845624 | snp | C/G | 0.140581 | 0.224783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791598 | TACACATAGACTAAT[C/G]TAATAGAATTGAAAA | 57626 |
rs75848825 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035346 | CAGAAAAACAAACTT[C/T]ATATGTTCTCAATTG | 57626 |
rs75849568 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080457 | CTAGAGGCTCTATTT[C/T]CTCTTTGCTGGATGT | 57626 |
rs75870282 | in-del | -/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70061351 | TTCCATTTTTTTTTT[-/TT]CTGACTAGTAACATG | 57626 |
rs75887438 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816279 | CTTTTTTTTTTTTTT[G/T]GGAGACAGTCTCCCT | 57626 |
rs75897685 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937643 | GAATTAATTTTACAC[C/T]TCTACCTGATGCTGA | 57626 |
rs75898010 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855363 | ACAGACAGATAGATA[C/T]ATAGAGAGATAGATC | 57626 |
rs75902898 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032254 | ATACTAGTAATTGTT[C/G]TGACAATGCGCAAAA | 57626 |
rs75905594 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988715 | CTCTGATAATTAGTG[A/C]TGATGAGCATTTGTT | 57626 |
rs75908792 | snp | G/T | 0.172674 | 0.237741 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076172 | AAAATACACAGAAGA[G/T]TCAATGCAACGGTTA | 57626 |
rs75915220 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821791 | TACTTTATACTTCTT[C/T]ATAAATAATCATCAC | 57626 |
rs75932147 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079617 | TTTCAACATTTTCAA[C/T]GAAGGAATAGCAATA | 57626 |
rs75940904 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951302 | ATAACTTGGCTTATG[C/T]AAGTGGCTTATTTTT | 57626 |
rs75945927 | in-del | -/CTTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884940 | TTTCTTTTCTTTTTT[-/CTTTT]TTTTTTTTTTTGAGA | 57626 |
rs75949187 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012091 | AAGACCCACCCCCAT[G/T]ATTCCATTATCTCCC | 57626 |
rs75950536 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998654 | CTTAATTAGTTTGCT[A/C]TTAATAGTAATGGAT | 57626 |
rs75959747 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847415 | TTAGCAAAAAAAAAA[A/G]AAAAAAAAAAAACAT | 57626 |
rs75966962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904532 | TCTTATTCCCATTAG[A/C]CCTGGTACTATATAA | 57626 |
rs75971151 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044138 | AGCTTCCTTCTTTTC[C/T]TATCTCTTCTCTTAC | 57626 |
rs75986959 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725299 | ACAATTGTCTGTTAA[C/T]CCTCATGTCTTGATG | 57626 |
rs75990668 | in-del | -/AAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69958262 | AATAATAATAATAAT[-/AAT]GTAAGTCTACATGTT | 57626 |
rs76011701 | snp | A/G | 0.103438 | 0.202533 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929454 | AGGGTAAAATTAAAA[A/G]GGGTAGCCTAGACTT | 57626 |
rs76023102 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900079 | AAACTACATAGGTCT[C/G]CTTCAACCTTGGAGC | 57626 |
rs76048644 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914532 | ACTTGACAGCAGAAT[C/T]TGCAGCATTTAAAAG | 57626 |
rs76049167 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799500 | TCCTGTAACTTCAGT[C/T]TTCAAAAGTGACCTA | 57626 |
rs76051615 | snp | C/T | 0.14665 | 0.227637 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778548 | GACATAGTTCTTGAT[C/T]GTACAAGAGATATCT | 57626 |
rs76064534 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048037 | TTACTTTTTCTGTGC[A/G]TAAGGGGGTGGGACT | 57626 |
rs76074501 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889570 | ACCTATGTAACATAT[A/G]TGCACCCTTACTCTT | 57626 |
rs76079276 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946752 | TCCTGGCCCCAAGCC[A/G]TCCTCTTGCTCTGGA | 57626 |
rs76087147 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710917 | CAGAGTGTGAGCTCC[A/G]TATCAGAGACTCTAT | 57626 |
rs76091962 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999499 | ACAGACCTAATTTCA[A/G]GTATAAACTTTCCCT | 57626 |
rs76091983 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69734565 | AATAAACATAGCCTC[A/C]GTGTATGCTTGTTTG | 57626 |
rs76111080 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056891 | ACAAAACAACTTATC[A/G]GTTCATTTTAAAGAA | 57626 |
rs76121261 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737319 | GTATTTGCATACTTA[C/T]GCTCTGGAAACTCCC | 57626 |
rs76130333 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745092 | AAGGAGAGGAACCCC[A/G]TTGTCTGATAATCTC | 57626 |
rs76142805 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028699 | GAATATTCATAGGCC[A/G]GGCATGGTAGTTTAT | 57626 |
rs76150816 | snp | G/T | 0.0770498 | 0.180522 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046159 | GAGGATACAACCAGT[G/T]AAAAGACAGGCAAAG | 57626 |
rs76153353 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885988 | TCAGGGAGTATAGTA[C/T]GTGATGCCATAGTTG | 57626 |
rs76183847 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720800 | AGTGTGGCTGGGGCA[A/G]AGGCTGAGGTGAGAG | 57626 |
rs76188093 | snp | A/C | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952668 | TTTACTTCCAGCTAA[A/C]ATGTGTTTTCCTGGT | 57626 |
rs76189789 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883506 | TCACTATCCCCTTGC[A/G]GTGTGTAGTGGGTGT | 57626 |
rs76197643 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805337 | AAAATCCAGCATTTT[C/G]CTTGCTATTAAACTA | 57626 |
rs76197987 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088642 | CAGCTACAATCACGC[C/G]ACTGCACTCCAGCCT | 57626 |
rs76235633 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752713 | TGGGGGTTTAAAGGT[G/T]GGGTAGAATTTTGAC | 57626 |
rs76242607 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011128 | ACCAAAAGTAAAATG[C/T]CCAAGAACAAAGTCC | 57626 |
rs76251627 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69918378 | ATTAAATACTACATA[A/T]TTTCTCCCAAAATAG | 57626 |
rs76252327 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864879 | GAGTGCTGTAAGAAC[C/G]CTGAGGAAGAGCACC | 57626 |
rs76264806 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964773 | TATTCATTGTTATCT[A/G]TCTTCTCCTATAAAT | 57626 |
rs76264917 | snp | A/G | 0.111224 | 0.207945 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933280 | AAGATAACATTAAAA[A/G]TCATTTAATACTAAT | 57626 |
rs76267086 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735556 | AATTATTAATGTATA[A/C]ATAGATATAAATAAA | 57626 |
rs76267666 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914597 | ACTAAAAATGTTATT[C/T]TGCCAGATAATGAAA | 57626 |
rs76267849 | snp | A/C | 0.162581 | 0.234218 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039714 | GTGCCATCTCTGCTC[A/C]CTGCAACCTCTGCCT | 57626 |
rs76275512 | snp | A/G | 0.103438 | 0.202533 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749046 | AAGGAATATATTTTT[A/G]TAGATTGCCACAATA | 57626 |
rs76287739 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036642 | ATTTTTGAGTTTAAT[C/G]AATGTTGATGTATGT | 57626 |
rs76304231 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047015 | GAAGTGTTGAATAGT[C/G]TGCTCAATACAATGC | 57626 |
rs76314026 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926057 | TTCATTCTCTTTTAA[A/C]CTTGCACAATATTCT | 57626 |
rs76315146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981517 | CTGAATGTAGTAAAA[G/T]ATGACTTTATTTAAG | 57626 |
rs76316843 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059169 | GCAACAGAGTCTCAA[A/C]AAAAAAAAAAAAAAT | 57626 |
rs76341614 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039400 | CTTTTATCATTTTCT[A/T]ATTTGACTTTTTGTT | 57626 |
rs76342967 | in-del | -/AT | 0.308908 | 0.242961 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946494 | ACATTGAGGATTGTG[-/AT]TTTTTTTCTTCTTTG | 57626 |
rs76344813 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012019 | GCAGGGGAACTCCTC[C/T]TTATAAAACCATCAG | 57626 |
rs76350816 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780899 | ATTCTGTTTCCCTGA[A/C]ACATGAGCATTTCTG | 57626 |
rs76364675 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021042 | ACCTTATTATTACCT[A/G]AAGTCCATAGTTTAT | 57626 |
rs76379036 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104340 | AAGGTAAGAAAAAGG[C/T]TGGGTTTTGGCCCTA | 57626 |
rs76379076 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70003422 | ATGACATGTTAAATA[A/C]ATTCAATTGATATTT | 57626 |
rs76384456 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855401 | AGAGATAGAGATAGA[C/T]AGAGATACAGATAGA | 57626 |
rs76400912 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865791 | CATTGTTACTGGACA[C/T]GGAATAAGGACAAAA | 57626 |
rs76402526 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69775221 | TGCATTGGAAAGTTT[A/G]CTACCTTTCACAAAT | 57626 |
rs76403230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909906 | GGCATTCAGTCAACC[A/G]TGGAGTCCTCCTTAA | 57626 |
rs76404295 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777854 | TCCTTGAATACAATA[C/T]CTTACTTATCATTTT | 57626 |
rs76414715 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759583 | GACAAAGTAGATCTT[A/G]TAAGTTTCATTAAGA | 57626 |
rs76421386 | snp | A/G | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826202 | GAGAAATGTTGGTCA[A/G]GGAACACAAAATTTT | 57626 |
rs76438438 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732657 | TGTTTGTTTGTTTGC[C/T]TTTTTTTTTTTCCTG | 57626 |
rs76456755 | snp | G/T | 0.0901694 | 0.192235 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732700 | CATCCTTTTCTCACC[G/T]TAGCAGCCCTGTAGC | 57626 |
rs76458294 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793774 | AAACCCAATCCTGCC[A/G]ATTATACTGAAGAGA | 57626 |
rs76462618 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69709662 | TTAAAAAATAAAGTC[A/C]TTATTTTTGTTTGTT | 57626 |
rs76467557 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047199 | AAACACAGTATTGTA[G/T]ATATGAAACATAAGA | 57626 |
rs76487731 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948129 | TATAATCTCTCTTAG[C/G]AAGTCCAGAGGAACT | 57626 |
rs76498099 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895711 | TGTTTCTTTCTTTTT[C/T]CCTTTTTTTTTTTTT | 57626 |
rs76498247 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996523 | CCCTTGAAACTTAGT[A/G]TGAAGCTGTCAACTT | 57626 |
rs76499142 | snp | C/T | 0.384209 | 0.210922 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075760 | ACACACATACACACA[C/T]ATATATATATATACA | 57626 |
rs76507045 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895188 | TAACTTCAATAATTT[C/T]AACAGGCACTGAATG | 57626 |
rs76512077 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847420 | AAAAAAAAAAAAAAA[A/T]AAAAAAACATAATTT | 57626 |
rs76514715 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885898 | GACCTAAAATATTAG[A/G]AAGGAGTTTAAACCA | 57626 |
rs76532127 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985145 | AACAACAACAACAAC[A/C]AAAAACCTCTGTGCA | 57626 |
rs76541822 | in-del | -/T | 0.089084 | 0.191327 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846100 | AAACTAAATAACAAG[-/T]TTTTAAAATCCTGTT | 57626 |
rs76542809 | snp | C/T | 0.105569 | 0.204058 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017187 | CTGAAAGAGCTGTTA[C/T]ACAAACAGATCTGAA | 57626 |
rs76544854 | snp | A/G | 0.152667 | 0.230274 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721160 | CATCCCTCTGCTCAC[A/G]GAGATAAGTGAATAT | 57626 |
rs76546179 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809601 | ACTTGCTATCACAAA[A/G]GCACACAGCCCATAG | 57626 |
rs76570646 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865737 | GAAAACAATAGCTGT[C/T]GAGAAAACCTTTATT | 57626 |
rs76575305 | snp | A/T | 0.331874 | 0.236213 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082754 | AATTGAATAAAGAAA[A/T]TGTGGTACATATACC | 57626 |
rs76592034 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69822569 | ACGCATCAGAGTTGG[C/G]CATTGCAATGGTCTC | 57626 |
rs76598888 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943155 | GCTCCATCATGATCA[A/G]GAGGCTCATGATGTC | 57626 |
rs76607243 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747246 | CCAGAAGTTAAATTT[C/G]TGAGTTAGCTTTTAA | 57626 |
rs76626589 | snp | A/G | 0.158632 | 0.232706 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055683 | GAGTATGTAGTGAAA[A/G]TGTAGAGTTTTTAAC | 57626 |
rs76629208 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804313 | ATTTTTTTGTGGGGG[C/G]GGGAAATAGTAATTA | 57626 |
rs76642948 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931895 | CATGGATGCATCTTG[G/T]TATGCATTTGTTTCT | 57626 |
rs76643702 | snp | A/T | 0.140581 | 0.224783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791807 | AATTTAAGACCTTAA[A/T]TGTTTGAAATCTAAA | 57626 |
rs76647125 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766731 | GACTGGAAAATGGAT[A/T]AGATTCTCTTAATGA | 57626 |
rs76669614 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899065 | GGGTGTCTAGAGTTA[A/G]CTAGAAGAAAGAAAC | 57626 |
rs76671379 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865284 | TAATTAAGTGTATGC[A/G]TGTCTGAGTATGAGG | 57626 |
rs76677930 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793892 | TGGGAGGAAAACTTG[A/G]TATGTTCTTTTTTTA | 57626 |
rs76679289 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727851 | AAACACATCACTGCT[C/T]TTTTTTTTTTTTTAA | 57626 |
rs76684834 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820956 | GCAATAGTAAAAGTC[A/G]TAAGCTCTGTGGATC | 57626 |
rs76722439 | in-del | -/CT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884937 | CTTTTTCTTTTCTTT[-/CT]TTTTTTTTTTTTTTG | 57626 |
rs76723914 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716455 | AATGTTAATAATTGG[C/T]ACAGAGAAATAAAAC | 57626 |
rs76743567 | snp | G/T | 0.100588 | 0.200439 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908997 | TTAAAGGCAAATTTA[G/T]TTCCTAAATATGGCT | 57626 |
rs76744535 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096602 | CTTTTATTTTTTCCT[A/G]TCGAGTTCTTTGAGC | 57626 |
rs76748996 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887600 | AAGTTCTTCTTTCCA[C/T]AAAACGCTGGGATGC | 57626 |
rs76764434 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70037200 | GAATATTTTCCTTCA[G/T]GCATTCTTGATAAAG | 57626 |
rs76764720 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781982 | TTATTCAATACTCAA[A/T]TGCAGCAAACATTTT | 57626 |
rs76765980 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004035 | ACAATACCTCTTAGA[C/T]ATGGTTACTAGTTTA | 57626 |
rs76767566 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890832 | TATTGCTTTAGAAAT[G/T]ATAAAACAACAATCA | 57626 |
rs76771207 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983618 | AGAGAAAAAAAAAAA[A/G]AAGCTGTGTTTGATG | 57626 |
rs76778170 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051236 | AAATTTTATTTAATC[A/G]TAATTAGTAATATCA | 57626 |
rs76784749 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903338 | GGCTTGGAAACCAAC[A/C]AATTCCAGCTCATTT | 57626 |
rs76800548 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789946 | GGTAGAGGCAGAGAC[A/G]CCAGCTGAAGCATCC | 57626 |
rs76809992 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842620 | AGCCACTATGGAAAA[C/T]AATGTGGAGATTTCT | 57626 |
rs76829342 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862855 | TAAATTTGCAGGCAC[A/C]TTGATCTTGGATTTT | 57626 |
rs76830026 | snp | A/C | 0.216048 | 0.247684 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074011 | TTGTATTTTTACTAG[A/C]GATGGGGTTTCTCCA | 57626 |
rs76837640 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843812 | TGTGTTAGCTTAGAC[G/T]TTTTTTTTATACTTT | 57626 |
rs76857750 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754683 | TCCTAATACAAATGC[C/T]ATCAGGCACCTTCCT | 57626 |
rs76863813 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69917781 | TGGTATCACATAACA[C/T]TCCACGTATCTTTTG | 57626 |
rs76875650 | snp | A/T | 0.113334 | 0.209338 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042830 | ACAGCTCCATGCTAG[A/T]CATTGCCCCTGAAGA | 57626 |
rs76892219 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789582 | GTAGTTGTGAGAATT[C/T]AATCAGTTAACCAAT | 57626 |
rs76901824 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735984 | TGTATGCACATATAC[A/G]GTGTTAAGTCACTTT | 57626 |
rs76904020 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728398 | AATTACAACTGCCTT[G/T]TAAAAATTGTTTGTT | 57626 |
rs76910172 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773446 | TATGAGATATAATTG[C/T]ATATTTAGTATTATT | 57626 |
rs76916335 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957388 | TATTCTATCAGTTTT[C/T]TATACAGATGGTTCC | 57626 |
rs76922932 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771280 | TTAGCAACTTTCAAA[A/G]AAAAAAAAAAAACAT | 57626 |
rs76932328 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944051 | CATCCTCTGAAAGGC[C/T]TGCTTTCAAGGTTTG | 57626 |
rs76946944 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966153 | ATAAATTTTCAGTGT[G/T]GACCATATATATAAA | 57626 |
rs76951131 | in-del | -/TTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69871739 | AACTTTTTTTTTTTT[-/TTTT]CCTGTGGTGGAACAA | 57626 |
rs76953555 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828976 | CTACCTGCTTTGGTA[A/G]TCAAAATGAAAGACG | 57626 |
rs76989650 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897726 | GTCCCAACAGGTTTG[A/G]CCCACCCATGGTGAG | 57626 |
rs76995439 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944974 | ACATTAAACTATAAA[A/C]CTTCTTTTTTTTTTT | 57626 |
rs77000301 | snp | A/T | 0.084364 | 0.187256 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852837 | GAAATGAGTTGTTCA[A/T]ACATCTTTACTGAGA | 57626 |
rs77010955 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821717 | ATCAAAGTGGCCTTC[C/T]GCTGTACATAAAATA | 57626 |
rs77026269 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067474 | GACTTGGACCTTGTA[A/T]GGGGAAAGCCGGTGG | 57626 |
rs77027919 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730589 | ATTCCTTTTTTTTTC[C/T]TGGATACAGGATCTT | 57626 |
rs77035429 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871708 | GAAAACCCCAGAACA[C/T]GGACACAATTCGGCC | 57626 |
rs77037285 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833445 | GCTATTGTCAAAAAA[A/T]AAAAAAAAATAGATG | 57626 |
rs77053747 | snp | A/C | 0.0737376 | 0.17729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758031 | AGCTAAAGTGGTAAT[A/C]AAAGGTTTTTTAAAA | 57626 |
rs77056764 | snp | A/G | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842568 | AATGAGGAGAAAATG[A/G]AACTTACATAGTGTT | 57626 |
rs77079285 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781663 | TCATCTTTTTACCCA[G/T]GATATTCTGAAATAG | 57626 |
rs77097083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021674 | TCCTTGCCAGCATTA[A/G]AGTTCTGGATTTGGG | 57626 |
rs77100589 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70003424 | GACATGTTAAATACA[C/T]TCAATTGATATTTTA | 57626 |
rs77103392 | snp | G/T | 0.0803491 | 0.183626 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876232 | CTGTGATTTCAAAAG[G/T]CTCCTTTTATATTGA | 57626 |
rs77110419 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100956 | TAATTCCAACATATG[C/T]TACAGATAACAGTTT | 57626 |
rs77136217 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70063727 | ATATTTTTTTAAAAA[-/A]TGCATTTTAAAATGT | 57626 |
rs77137157 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894908 | TGGCATGCACCTTGC[A/G]GTTGAGCAGAACCAA | 57626 |
rs77139235 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106977 | AGTTCAATTGGTGGC[C/T]ACAACTTTGAAAACT | 57626 |
rs77145153 | snp | C/T | 0.105569 | 0.204058 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012562 | CTATTTGAATGGTAG[C/T]ACCTATTATTAAACA | 57626 |
rs77147229 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017561 | CTCCACACCTGGATT[G/T]CCCTTGGCAGGTGTG | 57626 |
rs77155742 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926453 | ATAAAATAAGAACCT[C/T]GATTTCCTCATAAAA | 57626 |
rs77160737 | snp | A/C | 0.0799831 | 0.183287 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056315 | ATATATATGCACTGA[A/C]TACTGGGACACCCAG | 57626 |
rs77164602 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791346 | TTTATTTTTTTTTAC[A/G]TGGCAATACTCACAA | 57626 |
rs77165599 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994392 | AGGAAACCTGCCTAC[C/T]CTTGAAGCTAATCTC | 57626 |
rs77171206 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079851 | CATACTGAGCTTTAA[A/G]TCCATACCTTGTGTG | 57626 |
rs77179814 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951713 | ATCTTGGTTTCCAAA[A/T]TATGCTTCATATGTT | 57626 |
rs77184274 | snp | C/T | 0.16911 | 0.236552 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775353 | TATGTCTTGTAAAAA[C/T]AAGCATCTATTAATA | 57626 |
rs77199265 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817359 | CATGTAGTAAAAGAA[C/T]ATGAGGTTCCAGTGA | 57626 |
rs77199807 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017373 | TTCTCCTCATCCAGA[A/C]ACAATTGCCCACATC | 57626 |
rs77218935 | snp | A/G/T | 0.00557734 | 0.0525397 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853045 | ACTTACAGTTAAGCC[A/G/T]CAGTATATTAGGCTG | 57626 |
rs77222583 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70076215 | AGTCGGAGGATTGAC[A/T]CTACACAACTTCCAG | 57626 |
rs77225123 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061903 | CAAATCAGGGTCATC[A/G]GCATGTATATCAACT | 57626 |
rs77236756 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938527 | TATTAAATTAATAAT[C/T]TGCAACTAGACCAGA | 57626 |
rs77248278 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931296 | ATTGGTGAAATAGTT[A/C]ATTTTGCTGAAAAGT | 57626 |
rs77252944 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722923 | GGAATCAACTAAATG[C/T]TCAACAATGGATAAA | 57626 |
rs77258175 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70087557 | TTAAAAAAAAAAAAA[-/AA]GAAACTTAGTTGTGA | 57626 |
rs77276313 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001979 | CATATCTTAGAAGAA[A/C]TAGAAAATAAAGTAA | 57626 |
rs77280428 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063433 | CCATCACATGGCTTC[C/T]GACTTGATCACTAGA | 57626 |
rs77283247 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007445 | GCAATATTTCATCTC[A/C]AAAAAAAAAACACAA | 57626 |
rs77284552 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093131 | ATGATGCGCTATTAT[A/C/G]TAATTATGTGATTGT | 57626 |
rs77293937 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967914 | AAGAAATAAAAAAGA[A/G]TATTACACAAACTTA | 57626 |
rs77315739 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093857 | GCAGTTTTACTGTGA[A/G]CTGTCTTATTATACA | 57626 |
rs77316700 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884138 | CTGTGTTACAGTATG[A/T]CCTTGGAACTGAAGT | 57626 |
rs77318314 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896421 | GATAAGTATTTGAAT[A/G]ATCAGGACACCTTGG | 57626 |
rs77326710 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69946494 | ACATTGAGGATTGTG[A/T]TTTTTTTTCTTCTTT | 57626 |
rs77333700 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924729 | ACAACAAGAAGGAGA[A/G]AAGAGCAGCCGCCCT | 57626 |
rs77338103 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719731 | TGTTAAAGATACTCA[A/G]TAAATGATCATATAT | 57626 |
rs77341804 | snp | A/T | 0.229429 | 0.249152 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815546 | CAAGTAACACTGGGG[A/T]TTCCAAAACTGGGGA | 57626 |
rs77342062 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874181 | TGCACCTCCCTTTAG[G/T]GTTTTCCCTCTCACA | 57626 |
rs77345176 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69904468 | CTGAAAGAGCTGAAG[C/T]TGACTAGTAATACAG | 57626 |
rs77348176 | in-del | -/AAAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69967897 | AATCAAAAAAAAAAA[-/AAAA]GAAATAAAAAAGAAT | 57626 |
rs77352484 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920374 | CCATTTGTGGTTCAC[A/T]GTGCTATTTTAAGAA | 57626 |
rs77405054 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896685 | ATTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTCA | 57626 |
rs77408634 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69918379 | TTAAATACTACATAT[C/G/T]TTCTCCCAAAATAGT | 57626 |
rs77412148 | snp | G/T | 0.140581 | 0.224783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792065 | AATCACCATGGCACA[G/T]GTTTACCTATGTAAC | 57626 |
rs77418793 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69973157 | TACTTAAAAATATGC[A/C]TAACAGTAAACAGAA | 57626 |
rs77437129 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747211 | GGAAGCTTACTCAGA[G/T]AGCAGATACTCCATC | 57626 |
rs77440468 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738303 | AAGAATCTACACACA[A/C]AAATGCTGAAAACTC | 57626 |
rs77444207 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901237 | GAAAACAGAAAAAAA[A/T]TGAAAAAGAACCCAC | 57626 |
rs77459987 | in-del | -/C | 0.299158 | 0.245119 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942463 | TAGATTTCTCCTTTT[-/C]ATCATGAATAGTTTT | 57626 |
rs77463458 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912500 | ACTTCTTTCAACAAT[A/G]TATCAGGAAGCAATC | 57626 |
rs77475549 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018059 | ACTAGCGCAAAAAAA[A/G]GTTGAAAATTTATCT | 57626 |
rs77499526 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928393 | TCTCATATGTCAGCC[A/G]TATGAATAAACCTCT | 57626 |
rs77523131 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996635 | CACTTCAATGTTTTG[C/T]TACAGAAGAATCACA | 57626 |
rs77523683 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721569 | AATCTATAATATTCA[-/A]TTTCTAAATAAATGC | 57626 |
rs77532219 | snp | A/G | 0.142609 | 0.225759 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713963 | AAAAAAATCTCCTCA[A/G]TATATTCAGGGTGTT | 57626 |
rs77532795 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795892 | GTCCTCTTCCCCACA[A/G]ATTTTTCAAGGTGGA | 57626 |
rs77538159 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095851 | CCACCACACTCGCTA[A/G]TACTCTTTCCAGATG | 57626 |
rs77555090 | snp | A/C | 0.046775 | 0.145601 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815766 | AGGTGATTAACTTTT[A/C]CTTCTAGGTGGCCCA | 57626 |
rs77562618 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048720 | CTGACAGGAGGAAGA[A/G]TTCAGGCAGTGATGC | 57626 |
rs77567266 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792851 | CCACAGAGATAAAAA[G/T]CAGATTAATTGCTGC | 57626 |
rs77569527 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911542 | GCTCAAATCTTGGCT[A/G]CAGCTAGGTATAGGA | 57626 |
rs77587734 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804454 | TAAAAAGTTTTCTCA[A/G]CTGACAAAAGAGATG | 57626 |
rs77588952 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69822568 | CACGCATCAGAGTTG[A/G]GCATTGCAATGGTCT | 57626 |
rs77607540 | snp | C/T | 0.0944967 | 0.195752 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959400 | TTATCCTGGCTACCT[C/T]TTGGCTCAGAGGTAA | 57626 |
rs77615887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970640 | CTCTCCTGACTCTCA[A/G]CCTGTGGGTGGATCT | 57626 |
rs77623707 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813818 | AAATTGCTTTGGGCA[G/T]TATGGCCATTTTAAT | 57626 |
rs77628493 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754549 | TATTTTACTTTCCAA[A/C]TGGATTGTAAGCTTT | 57626 |
rs77639570 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849520 | TTACTGTCCTTAATG[C/T]CTTTTTCCTCTGGGG | 57626 |
rs77644863 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051132 | CAAAGTTAGATTACT[C/T]TACAAAATATTCATT | 57626 |
rs77647713 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064871 | TGATAAATTTTGACT[A/T]ATGTGTACATGTATG | 57626 |
rs77654564 | snp | C/G/T | 0.461481 | 0.133325 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855349 | AGATAGATAGATAGA[C/G/T]AGACAGATAGATACA | 57626 |
rs77667178 | snp | A/G | 0.142609 | 0.225759 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715130 | ATAGCTATTGTATCA[A/G]CTAACGATTGCTGCA | 57626 |
rs77676799 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087564 | AAAAAAAAAAGAAAC[C/T]TAGTTGTGATGAGAA | 57626 |
rs77676920 | snp | C/T | 0.116838 | 0.211584 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979535 | ATTTTAGCAAATTTA[C/T]ATTATGTATTTATCA | 57626 |
rs77692677 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808637 | GAGAAACAACCAGCA[C/T]AAAAACTCCAGCAAT | 57626 |
rs77697559 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742352 | CTTTTAAATATATTC[C/T]GGAAAAAAGGACACT | 57626 |
rs77703877 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063176 | AGATCCAGCTCTGAT[G/T]ACTTCTCTAAGTAGA | 57626 |
rs77704464 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885437 | TTATTTTTTTTTTTT[C/T]TTTACACTTCATTGA | 57626 |
rs77723045 | snp | C/T | 0.16911 | 0.236552 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773521 | CTCAGTAATAAATGG[C/T]AATAAGAGAACATGT | 57626 |
rs77727399 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034285 | ACTGACGAATTTTGA[C/T]TGTAGAAAGTACTCT | 57626 |
rs77738217 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847418 | GCAAAAAAAAAAAAA[A/T]AAAAAAAAACATAAT | 57626 |
rs77747487 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053883 | TCCTTCTTACTGTCC[A/G]ATAGGGAATGCGTCT | 57626 |
rs77747876 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798098 | TCCCAAATGTTTATA[A/T]GATAATATAAGCTAA | 57626 |
rs77749852 | snp | A/C | 0.0759472 | 0.179459 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820851 | GTCAAACAAATGTGA[A/C]GTTTGGCACTAGACA | 57626 |
rs77756912 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781500 | TCTAGCACCTAGGAT[G/T]GATACTCAAAAGCCT | 57626 |
rs77764429 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940405 | GTTTTAAGAATTTTG[C/T]ATTTCGTATTTCATG | 57626 |
rs77764462 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951279 | GAAATAAAACTAAGA[C/T]AAAAGCCATAACTTG | 57626 |
rs77767514 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69754009 | GCCTGGCTAATTTTT[C/T]TTTTTGTTTTTAGTA | 57626 |
rs77769815 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079909 | AAGTGAAGAGTTTTT[A/T]AGAACTGAATCATTT | 57626 |
rs77786747 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899191 | ACTAGAAATGTGATT[C/T]GACTCGATTTGTTGC | 57626 |
rs77790836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863468 | GTTGAATGAATTCTG[A/G]ATAGAGTGTATATGA | 57626 |
rs77795185 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885709 | CTTTCTTAGGTTTAT[C/T]CAATCAACCATTCAG | 57626 |
rs77797862 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982556 | GACTGAAAGAGAGAA[C/T]GAAAGTAAGAAAGAA | 57626 |
rs77807370 | snp | A/T | 0.0839998 | 0.186933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837374 | ATAATTAGTAAGCAA[A/T]TTGAAATGTCTTTCA | 57626 |
rs77811335 | in-del | -/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885435 | TGTTATTTTTTTTTT[-/TT]CTTTACACTTCATTG | 57626 |
rs77856066 | snp | A/G | 0.0596104 | 0.162024 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109302 | TTAATGAGCCATTAA[A/G]ATAGAACCCAGTAGT | 57626 |
rs77865165 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710741 | CTCTGTCATTTTCAG[A/G]TTATGTTTCTGAAAA | 57626 |
rs77871760 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718258 | ACTGCTCTCCCAAAA[A/G]GCTTTCTGTGGCCAT | 57626 |
rs77882787 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992955 | CCTTTCTTACAGTGT[C/G]AGTAACTCAGCTGAA | 57626 |
rs77886777 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884445 | AAAAAAAAAAAAAAA[-/AA]CTACGTGAAGCTAAA | 57626 |
rs77902004 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939785 | TGTATCCTTTGCAAT[A/G]TCTTTTATGATAAAC | 57626 |
rs77904100 | snp | A/G | 0.095934 | 0.196885 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936508 | ACAGGAGAATTGCCC[A/G]AACCTGGGAGGCGGA | 57626 |
rs77910058 | snp | A/T | 0.0535932 | 0.154675 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865522 | TGTGTTTTTAAAAAA[A/T]TTACTGAAGAGGGAC | 57626 |
rs77914272 | in-del | -/ATGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69750506 | ATTAAATATACATGT[-/ATGT]GTGTATATATATGCA | 57626 |
rs77935105 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026718 | GGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 57626 |
rs77935479 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019186 | CTAATTCAGGAAAGG[C/T]TGTCTCTGTGTTATG | 57626 |
rs77937779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011461 | GATATTTTGTTTGCC[A/G]TAGATAATAAATTTT | 57626 |
rs77945426 | snp | A/G | 0.193653 | 0.243567 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948417 | ATCATTATGAAAGGG[A/G]TGAAACACAAATAAT | 57626 |
rs77951954 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913298 | GCTTCCCAGGAGGCA[A/G]GGAGCTATATCCAAA | 57626 |
rs77983781 | snp | A/G | 0.142609 | 0.225759 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715007 | ATCATGATGCCAGAA[A/G]AATTCTGGGCAGCAT | 57626 |
rs78001762 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960259 | GCTGATCTTCACAAT[A/G]TCACCTCTTGTTTTT | 57626 |
rs78003117 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999902 | GGATACTAATATAGT[C/T]GGGATGTTTGTCACC | 57626 |
rs78018818 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758987 | CCCCAGGGTGTTCTG[C/G]GTCCCAAGAGCTTAC | 57626 |
rs78039833 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729292 | TATGAAATTGATGCA[A/G]TTTTGGTCTTGAATC | 57626 |
rs78044143 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69805856 | TTGTACAAGGAATTT[A/G]TAAAATTATACTGGC | 57626 |
rs78044551 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789119 | TATATTAAAATCTGT[A/G]TCTATCCTCTAAATT | 57626 |
rs78044826 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69898747 | TAATAATACCTAGTG[C/T]CATTGCCTCTTCTGA | 57626 |
rs78048976 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769336 | TATTTCATGTTCTAA[A/T]TCTCAGTGTATAATA | 57626 |
rs78050858 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994075 | TGATAAGCTTAGGGC[C/T]TATGACTCCAAATTC | 57626 |
rs78065407 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825063 | TGATAAAGCCATGTT[A/G]CATACTAGTAACGAT | 57626 |
rs78081700 | snp | C/T | 0.089084 | 0.191327 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000016 | ATGAACGGCTTGCTG[C/T]CATCCTTATAATAAT | 57626 |
rs78086358 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048743 | AGTGATGCCAGCGAT[A/G]GAGAGCAGTTGTAAA | 57626 |
rs78102845 | snp | C/G | 0.0737376 | 0.17729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789196 | GGAATCTTTAGGATC[C/G]ATCTATGCTATCAAT | 57626 |
rs78124287 | snp | G/T | 0.128288 | 0.218372 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077043 | ATGCAAAATGGTAAA[G/T]CCACCTTGGAAGAAC | 57626 |
rs78132458 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901880 | TTGGCTCAATGCAAC[A/C]TCTGCCTCACGGGTT | 57626 |
rs78152324 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960054 | TTAAGACCAAAAAAT[A/G]TCTAAGTATTTTCCT | 57626 |
rs78171470 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813943 | CTAGAATCCAAAGAA[A/G]TCCTAAGCAAAAAGA | 57626 |
rs78176007 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801050 | AGAATATACATTATT[C/T]GGGTGATGACTACCT | 57626 |
rs78180232 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828182 | GGCTTGCCACAGCAC[A/G]CTCCATGAACAGCTA | 57626 |
rs78184041 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945979 | TGCTTATTCAATGGA[A/G]TACTTCATAATAATA | 57626 |
rs78189401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928372 | ATTTGAGGTTTCCTC[A/G]TATCTTCTCATATGT | 57626 |
rs78193992 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725006 | CAAGTGAATGCTGCA[C/T]ATGTGGTGGGTTTGT | 57626 |
rs78195721 | snp | C/T | 0.328148 | 0.237472 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854933 | TGCCAACTGGAAATA[C/T]TGGAAATATATTTTT | 57626 |
rs78197225 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048045 | TCTGTGCGTAAGGGG[A/G]TGGGACTTTAGCTCT | 57626 |
rs78215659 | snp | C/T | 0.0498117 | 0.149749 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105463 | GAAACATTAATATTT[C/T]TAGGAGCTTATTCAA | 57626 |
rs78218325 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071966 | TAATAAAATTCACAA[C/T]AGAAATCAATTTAAT | 57626 |
rs78221819 | snp | C/T | 0.077417 | 0.180873 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006574 | GTTTGGTAGACTCCA[C/T]CAGTGAAGCCATTTG | 57626 |
rs78235439 | snp | C/G/T | 0.361474 | 0.223771 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855353 | AGATAGATAGACAGA[C/G/T]AGATAGATACATAGA | 57626 |
rs78237965 | snp | A/C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69943247 | TTTCTTCATTTAATT[A/C/T]TTTTATAATTAAAGA | 57626 |
rs78241465 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844954 | AAAAAATAAGTATTC[A/G]ATCCAGGAAATATTT | 57626 |
rs78268837 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797829 | GCGAGACTCCATCTA[A/C]AAAAAAAAAAAAAAA | 57626 |
rs78274284 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761831 | ATTAAAAGTTCTGCA[C/T]TCAATGACTCATCAT | 57626 |
rs78277216 | snp | G/T | 0.170084 | 0.236883 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016443 | CCGTAGGCTCGTAAG[G/T]GCCTGCTCTAGCTCC | 57626 |
rs78302566 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803763 | CTTGAAGATGGGTCA[C/T]ATAAGAAGGAATGCA | 57626 |
rs78305907 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774664 | TTGCCTTCACTTAAT[A/T]AAAAAAAACACACAC | 57626 |
rs78315327 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828748 | GCTGGCCTTGCTGGC[C/T]GTGTAGGACCTGGGT | 57626 |
rs78316087 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948096 | TTAGAGATTGTTTTC[A/C]AAAAAAAATGAAATG | 57626 |
rs78317005 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799197 | ACACAATCTCATTAG[G/T]CTCATATTTTCTGGT | 57626 |
rs78322122 | snp | A/G | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770304 | CAAGTGCAGCCTGCT[A/G]GCCCGAGTGGGCAGA | 57626 |
rs78327620 | snp | A/C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957489 | TTCCTTGATTTACAA[A/C/T]GAGGATAGCACATCC | 57626 |
rs78350577 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958749 | AAATTAAAAAAAAAA[A/T]ATACATATTATCAAA | 57626 |
rs78367858 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70102401 | AAATAATAAGGTGTT[A/T]TCTAACTTGGGCTAA | 57626 |
rs78372121 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70019364 | ACTGAGTAAGCTATA[-/G]AAAGTTAATGAAGGT | 57626 |
rs78391032 | snp | G/T | 0.10237 | 0.201756 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904877 | AATCTTCATTACCAA[G/T]GATTTGTAGTTAATC | 57626 |
rs78405585 | snp | A/T | 0.0520825 | 0.152737 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826927 | TTCATTTTCTGGACA[A/T]CCATTTTCTAGACAA | 57626 |
rs78415542 | snp | G/T | 0.0333238 | 0.124705 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764309 | TGTACATCACTTTCC[G/T]TTTTCTGTACATCAC | 57626 |
rs78427274 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807796 | ACAGGACTGGAGTGC[C/G]AGGAGTGTTGCTGAA | 57626 |
rs78431798 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947879 | TTTTAAAAAAGCATG[A/C]AAACTGCTAATGGAA | 57626 |
rs78452404 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959970 | CAATATCCTTGAATA[A/C]AGTCTTCTTTACCTG | 57626 |
rs78458856 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742809 | TTAAAATTAAAAACC[A/G]TAAACTTCAAATCTT | 57626 |
rs78460984 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793732 | TGAACGAGTAGAAAA[C/T]TAGCACAAACTGTTG | 57626 |
rs78465558 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064082 | TAGAGGACGGATTAA[C/T]GGACACAAAGACAGG | 57626 |
rs78468749 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755859 | AGTGGAAAAATCATA[C/T]GTTTTGAAAGCTGGC | 57626 |
rs78475060 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765089 | CCTGAGTACCTGGGA[C/T]TGTAGGCATGTGCCA | 57626 |
rs78475459 | snp | C/T | 0.192715 | 0.243348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905904 | AATAAGTCAAAGTTT[C/T]GAAAATGTACACATG | 57626 |
rs78481789 | snp | A/G | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842526 | AGAATGACTATTTAA[A/G]AAGACAAAAAATAAC | 57626 |
rs78491540 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990366 | TTCCAATTAAAAGGC[A/G]AAGAGTGGCAAGCTG | 57626 |
rs78493415 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726161 | CCATTATGTAAATAC[C/T]AGAATGTTTTGCTAA | 57626 |
rs78495716 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933928 | ATTCGACTTAATATT[A/T]TGGGCAATATGTAAT | 57626 |
rs78496777 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69860775 | TAATAGATAATAAAA[A/G]CAATGTGTTTTTATT | 57626 |
rs78506833 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771691 | ACGGTGAAGATATGT[A/G]GGTGCATAGTTTTTA | 57626 |
rs78510424 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765725 | TTTGACCAGAGCAGA[A/G]GTATACTTTGGAATG | 57626 |
rs78512884 | snp | G/T | 0.163892 | 0.234703 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818913 | ATTATATTGCTTTTC[G/T]TCAGAAAAAGTCATA | 57626 |
rs78512939 | snp | C/T | 0.295854 | 0.245759 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092854 | TAGCCACGCTTTCAG[C/T]GCTTGATGATCACTC | 57626 |
rs78512986 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703113 | TACAAAATACAGTCA[C/T]GCACTGCATAGCTGT | 57626 |
rs78513071 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898798 | ATCCTTGAGACATTT[G/T]TTTCTATTCAATGCC | 57626 |
rs78526078 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724254 | TGGTTGATGTATTAC[A/G]TCTCCATAAAATGTA | 57626 |
rs78537700 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69822571 | GCATCAGAGTTGGGC[A/T]TTGCAATGGTCTCCA | 57626 |
rs78548939 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091816 | CCTAAACTACCTTAG[A/C]GCTAACTTTCATAAA | 57626 |
rs78551412 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043976 | CAATTCTTACTCATG[C/T]TCACAACATTTTTGT | 57626 |
rs78552864 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930892 | ATTTATGCATATATG[C/T]GTTAATCAGTGACTA | 57626 |
rs78554593 | snp | A/T | 0.0482946 | 0.147699 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770642 | CTGTCCTAAGACATT[A/T]ATCTTTCTATTGTGG | 57626 |
rs78559462 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905857 | TGTCTAAAATAATCA[C/T]GATAAATGGCTTGGA | 57626 |
rs78569666 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023744 | TTTGACTGCTTTCTC[A/G]TGGTTGTTTTCTAGC | 57626 |
rs78585309 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69988702 | TATCACTGATCGTTA[C/G]AGAAATGCAAATCTA | 57626 |
rs78586396 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017908 | AAGTCTTATCCAATA[C/T]TATTAACTTTGTATT | 57626 |
rs78589048 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823387 | GTGAATATCATGCAC[C/G]CAAAGGTATTTGGGG | 57626 |
rs78591135 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922951 | AAGTGAATAAATAAT[A/G]CATAAAGATGAAATA | 57626 |
rs78593347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737266 | CTCATGGTGGCTGCT[C/T]GGGCAGGCAGCTGCT | 57626 |
rs78596256 | snp | A/G | 0.104859 | 0.203554 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005556 | TCTTCTTCCAATGTG[A/G]CCCAGGGTAGCCAAA | 57626 |
rs78603484 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017148 | GACATAGGACAAGAA[C/T]TCAGGACCTGCCAAA | 57626 |
rs78604373 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768677 | ATACATTGATGTTGA[A/G]CAGATATGAATAAAA | 57626 |
rs78611150 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761582 | ACCAGGAAAATACTA[C/T]GCCAGATTTTCATGC | 57626 |
rs78618543 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797830 | CGAGACTCCATCTAA[A/T]AAAAAAAAAAAAAAA | 57626 |
rs78633170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862420 | AATGGTAAAACATAT[A/T]CTTTAATTCCTACCC | 57626 |
rs78638901 | snp | A/G | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826152 | GAGAGTAGAATGGTG[A/G]TTATTAGGAGCTGAG | 57626 |
rs78639582 | snp | A/T | 0.077417 | 0.180873 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047709 | AAACTGAATTTTTTT[A/T]AAAAAAACACAATTA | 57626 |
rs78640804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840659 | TTAGCTGCCTTTCTA[C/T]GCACTTTTATTTTGA | 57626 |
rs78665223 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988750 | CAAAGGAAGACATAC[A/G]TGCAACCAACAAACA | 57626 |
rs78684203 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69803844 | ACAGTACCTCAGTTC[A/T]ACAACCACAAGGAAT | 57626 |
rs78685845 | snp | A/G | 0.120326 | 0.21374 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871233 | CTTTAAACCACAGCT[A/G]GAGCAGCCTGGATAT | 57626 |
rs78686489 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859128 | CAGAATATATTTAGA[A/C]TGTAACTGTAGAACA | 57626 |
rs78712109 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868437 | TTTAGATGATGGTGA[C/T]AATGAATGTTAAGAG | 57626 |
rs78714443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912410 | AAAATTGTATTGTAT[A/G]TGATGGCTTTCTCTC | 57626 |
rs78715879 | snp | A/G | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841886 | CAGAAATAAAGCCAC[A/G]TATTTACTGCTAACT | 57626 |
rs78724092 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065882 | TTCATCAAAACCAAG[A/C]TGAAAAAAAAAAACT | 57626 |
rs78737280 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885331 | CTTTTGGTAACCAGC[A/G]GCGTTGTTTGTACAA | 57626 |
rs78745799 | snp | G/T | 0.318695 | 0.24347 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945176 | ATGTTTAGAACAGAC[G/T]GGGTTTCACCATGTT | 57626 |
rs78770878 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993298 | ATGCAGTTTATATAG[C/T]ATTTTCACTTAGCAA | 57626 |
rs78804648 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918526 | TGCTTTTTTTTTTTT[C/T]TTTACCTTGCTTGCC | 57626 |
rs78805778 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69945710 | ACAAACACAATGACA[G/T]GCCACAACACCTCTA | 57626 |
rs78816219 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922633 | TGTATGATTTAATTC[A/C]GCTCCTGTGTAGCTC | 57626 |
rs78827544 | snp | A/G | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840550 | TAATCTGAATAAGAA[A/G]CATAATATTAGTTAC | 57626 |
rs78828157 | snp | C/T | 0.16911 | 0.236552 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960986 | GACAATTAGAATCTC[C/T]TTTCTTTCCTAAGCA | 57626 |
rs78841354 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983578 | GACCCTATCTTTACA[A/C]AAAAAAAAAAAAAGA | 57626 |
rs78843668 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735466 | AGAAAATCTATTATA[A/G]ATTGAATAGTAAATA | 57626 |
rs78851095 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936166 | TTCCAACAAGAGGAA[A/G]GTCTGAGTTAAGTAA | 57626 |
rs78858421 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894275 | TGTATCATTGGCCAG[C/T]GTAATCCTGCTTGTG | 57626 |
rs78867691 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848848 | AATAATGACATAATC[A/G]AAATAAGTAGAGCTC | 57626 |
rs78872836 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017237 | TGTTGCCAGTGATGA[A/G]GAGAAAAGAGCTGAG | 57626 |
rs78877773 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908382 | AATACAATAAAGAAA[C/T]GGTGTGAGAGAAGAT | 57626 |
rs78878064 | snp | A/C | 0.167513 | 0.239819 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708401 | TGGTGTGCCTCAAGA[A/C]GTAAGTTTTGATTAG | 57626 |
rs78881820 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884839 | GAGTCAAATTGAAAT[C/T]TATCTCGTAGGAAGG | 57626 |
rs78891114 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953369 | TGCTTTTCACTCAAT[C/G]TGACAATGACATAAG | 57626 |
rs78904810 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901820 | TTTTTTTTCTGAGAC[A/G]GAGTCTCGCTCTTGT | 57626 |
rs78912125 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769231 | TTTTTCTCTAGGCAG[A/G]GACTAAAAGAAGGGT | 57626 |
rs78925205 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066660 | TTCTCTTATTTGATT[A/C]TTCTTATCATTAGAA | 57626 |
rs78937067 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754929 | GAAGTTTTCTGTAAG[A/G]TTCTCTATTGTTTTA | 57626 |
rs78944031 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69965688 | TTGCCAAACACTTAG[G/T]CAAGTTGTGAATGCA | 57626 |
rs78944398 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751239 | GTTTGCTAACTTTCA[A/G]TTTTATTGTTATGCA | 57626 |
rs78948043 | snp | A/G/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69994759 | AAGCCTCTATTAATC[A/G/T]GAGTTCTAGAATCTG | 57626 |
rs78968771 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69702897 | CACCACTCTTATCTT[C/T]GTAATCACATCTTGT | 57626 |
rs78973071 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751248 | CTTTCAATTTTATTG[C/T]TATGCAACTTGCATT | 57626 |
rs78983457 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079493 | TCTCAAAAATTACTT[A/G]TTTTGATAATATCCC | 57626 |
rs78993898 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033604 | AGTCACCGCAACTGG[C/T]TTTTTTTTTTTTTTT | 57626 |
rs78994544 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70065526 | ATCAGTGACAAGAAA[A/C]CAGCCATTCTTTCAT | 57626 |
rs78996826 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074841 | TAAACAAATTTATCA[C/G]TATTCACAGCATGAT | 57626 |
rs79010026 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853132 | CTTTTTCAAAACAAG[A/C]ACTGTTAAACTACTG | 57626 |
rs79025248 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828983 | CTTTGGTAGTCAAAA[C/T]GAAAGACGTAATCTC | 57626 |
rs79053048 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949841 | GTTAACAATGACATT[C/T]AAATTTTACTGCAAT | 57626 |
rs79082600 | snp | C/T | 0.0822104 | 0.18546 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778240 | TAGTTATATAATCTA[C/T]GATGTCCTTGGGCTA | 57626 |
rs79084918 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730587 | CCATTCCTTTTTTTT[C/T]CCTGGATACAGGATC | 57626 |
rs79093590 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819631 | GCAAAAAAAAAAAAA[A/T]GTAGAAATAAAAGAG | 57626 |
rs79096720 | snp | A/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952819 | ATGGCTAAGTGGTAA[A/T]TTACAGAAGTCTTAA | 57626 |
rs79097834 | snp | C/T | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841402 | GTCAGCAGTGTTTCT[C/T]GTTTCTATATGCTAA | 57626 |
rs79110374 | snp | A/T | 0.0321726 | 0.122683 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821091 | TTAAAATTTGAATTT[A/T]AAAAAAATAAAAATT | 57626 |
rs79116569 | snp | G/T | 0.142609 | 0.225759 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715154 | TGCTGCATCTACTTA[G/T]AAAGCAGGGCTCCTA | 57626 |
rs79147307 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939493 | ACAATATGCTGTGAC[A/G]GAGAGGTTTAAAAAA | 57626 |
rs79156826 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809056 | ATCCTTCAAGAAATA[G/T]GGGATCATGTAAAAC | 57626 |
rs79162584 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949608 | CACAGCCTACACTTA[A/C]GGAGGGGGGAGTTGT | 57626 |
rs79164369 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828491 | GAAGGAAACCTCCAG[C/T]TGAACTTTCTAATAA | 57626 |
rs79169378 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032093 | CTGCAAATTATGGAT[A/G]CTTAATGGATATCTT | 57626 |
rs79192792 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963430 | AAAGTGGTTACTCTA[C/T]GGCAGCAACCAGAAT | 57626 |
rs79200254 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854815 | ACAAAACACTGTTAT[A/G]TGTGAAGGCCATAAC | 57626 |
rs79211897 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068418 | GTGACACTGATTAAT[A/G]AATTATGATTTTATT | 57626 |
rs79219994 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890268 | TTTGTAATAGATCAT[A/G]GATTCGGAAAGCACT | 57626 |
rs79223649 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091432 | CATAACTCATGTGTT[G/T]TTCTCTCAGCAAATA | 57626 |
rs79224864 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007444 | AGCAATATTTCATCT[A/C]AAAAAAAAAAACACA | 57626 |
rs79244104 | snp | C/T | 0.116838 | 0.211584 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711185 | ACATTACTTTCTTAA[C/T]AAATAGAATTGAGAA | 57626 |
rs79249645 | snp | A/G | 0.151001 | 0.229563 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719937 | ATAAAATATAAGACA[A/G]TGAACATAAACAGGA | 57626 |
rs79254047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892737 | ATGCATAATCAGAAA[C/T]AGCTAGACAGTTGGG | 57626 |
rs79254085 | snp | A/G | 0.113685 | 0.209567 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821718 | TCAAAGTGGCCTTCC[A/G]CTGTACATAAAATAT | 57626 |
rs79270270 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944977 | TTAAACTATAAAACT[A/T]CTTTTTTTTTTTTTT | 57626 |
rs79287403 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706243 | GACTTAGATCTCTTG[A/C]TATTTCCCCTTCTTT | 57626 |
rs79299895 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012979 | TAAGCCTATTTATCA[C/G]TTGTCGTTTAATTTT | 57626 |
rs79302839 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69775222 | GCATTGGAAAGTTTG[C/T]TACCTTTCACAAATG | 57626 |
rs79303832 | snp | C/G | 0.116838 | 0.211584 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042906 | GATATTGATGATCTT[C/G]CCCTTGTGTATATAT | 57626 |
rs79304704 | snp | C/T | 0.079617 | 0.182947 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869692 | TAAAATAATAAACTA[C/T]ATTTTTCTGATACTC | 57626 |
rs79313527 | snp | C/T | 0.067446 | 0.170804 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094995 | GCTACCAAAAAGTAG[C/T]TTCTTCCTTATGTCT | 57626 |
rs79336071 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911062 | CAACCCAGAAGGTAC[A/G]CTAGACAACTGCTAG | 57626 |
rs79336692 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855362 | GACAGACAGATAGAT[A/C]CATAGAGAGATAGAT | 57626 |
rs79342188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043451 | GCCAAAACATACAGC[A/G]TTTATACAGTCTATG | 57626 |
rs79343040 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983391 | AAGATCCCAAATATC[C/T]AAAGCCATTTTGAGT | 57626 |
rs79344638 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957537 | GCTAAGGAGCATCGA[C/T]ATATATAGTTTACAT | 57626 |
rs79366739 | snp | A/C | 0.0894459 | 0.191631 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851328 | CAAAATTATTTCTGA[A/C]TGGGCAACACAGACT | 57626 |
rs79369594 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963071 | TTTATAATTTCAGCA[C/T]TTTTTTTAGAGACAG | 57626 |
rs79369887 | snp | A/C | 0.139903 | 0.224452 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966367 | TGCTTTAGGAATGGA[A/C]CTATAAAGCCTGGAC | 57626 |
rs79376068 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753719 | TAGGCAATTGTCCTA[C/T]TTGAAGATTATTCTC | 57626 |
rs79377621 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797662 | TCTCTACTAAAAATA[A/C]AAAAAAAAAAAAAAA | 57626 |
rs79384385 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064116 | AACAAATCAATAATT[A/G]TCTATGAGGACTAAT | 57626 |
rs79386962 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849728 | ACTTGCAGAAAATCA[A/G]AAAAAAAAATCTGCT | 57626 |
rs79390555 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824685 | ATTTATGTGAAGTCT[A/G]CAAATAGGCAAAACT | 57626 |
rs79412558 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780217 | GCATGCATTATTGAG[A/G]GACTTAACTTTTTAT | 57626 |
rs79421149 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002426 | GGAAGGGAGAAAAAA[A/G]ATTTTTTTAAATGAA | 57626 |
rs79426988 | snp | G/T | 0.264084 | 0.249603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985306 | AAAACCAATCTGAGT[G/T]TAAAATAGGCAAAAG | 57626 |
rs79428115 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837400 | TTTCAAAAATTTAAT[A/G]ACATAATTTCACACA | 57626 |
rs79435649 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751677 | GGGCCTTGTATGCCA[A/G]TATGATTTATTTTAT | 57626 |
rs79439125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933580 | AAGTGAAGGATGTAT[A/G]GCATGTTTTTACTAC | 57626 |
rs79439783 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987210 | ACTAATTAAACCGAT[A/G]GTATTATTTCTGTTT | 57626 |
rs79440156 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017708 | AGCTCACTACTATCA[C/G/T]GAGCACAAAATCCTA | 57626 |
rs79451663 | snp | A/G | 0.396727 | 0.202413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785157 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 57626 |
rs79460924 | snp | G/T | 0.0737376 | 0.17729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807549 | CACACTCCCCATGTA[G/T]TTCACCTGAGAGGGG | 57626 |
rs79482954 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084649 | TTTTTTTTTTTTTTT[G/T]AATTTTTAGTAGAGA | 57626 |
rs79492279 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734994 | CATTTATAAGCAACT[C/T]TGATGCAAAGTCATA | 57626 |
rs79495014 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824687 | TTATGTGAAGTCTAC[A/G]AATAGGCAAAACTAA | 57626 |
rs79500197 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760319 | ATCTTTGGGGCAGGA[C/T]AGTAACTAAACCAAA | 57626 |
rs79516589 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077237 | AGGTGAAATGGGTAC[A/C]AAAGCAGTGGTACAC | 57626 |
rs79532887 | snp | A/C/T | 0.00517997 | 0.0506535 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076552 | AAATCTACATGACCT[A/C/T]GGGTTTGACAATGTG | 57626 |
rs79542479 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786422 | CCATGATTATCTCAA[C/T]GGATGCAGAAAAGGC | 57626 |
rs79548308 | snp | A/C | 0.172028 | 0.23753 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972470 | TTCATTTAAGTTTTC[A/C]TTTGATCATGAACAT | 57626 |
rs79570347 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754495 | ACAAAGTTTGTGTCA[G/T]ATGAAAATTGTTATT | 57626 |
rs79579089 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066512 | ATGAGCAGAATTCCT[C/T]TTCAGTGCTACATTA | 57626 |
rs79586714 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013292 | ACAAAAAAGAGAAAA[A/C]AAAGGGAATGCAGAG | 57626 |
rs79590245 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991835 | AGCCAGAGATAAACA[A/T]GATAGGAGAATTTAT | 57626 |
rs79590717 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734101 | GGGGTAATTGGGTCA[C/T]GGGGGCAGATTTCTC | 57626 |
rs79592474 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824374 | TCCCAAAAAGTAAGA[C/T]GATATTTTCTCTGAT | 57626 |
rs79604961 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109428 | ACCCCCAACAGAGCA[C/T]AGGAATCAACCACTG | 57626 |
rs79605435 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097579 | AATGTAATCTTGGAC[A/C]TCTTTATGTAGAATC | 57626 |
rs79612239 | in-del | -/ATG | 0.326976 | 0.237854 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953279 | TTCCTCAGGCTACTC[-/ATG]ATTTGATGTACAACA | 57626 |
rs79615662 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754669 | AGAAAAAAAAATCAT[C/G]CTAATACAAATGCCA | 57626 |
rs79623487 | in-del | -/G | 0.0737376 | 0.17729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811640 | AGAGCAGTTAGGCAA[-/G]GTTACAGAAATAAAA | 57626 |
rs79623628 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974019 | GAAAACTTTCCCCTG[G/T]TCTTCTTTAGGTGGG | 57626 |
rs79650444 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931061 | TACCCATATATCAGA[C/G/T]GTCAAATTAGAAACA | 57626 |
rs79663005 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065389 | CTAGATCATGGCATG[C/T]TAGCCAATTCTCCTA | 57626 |
rs79667321 | in-del | -/CTT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746355 | GCATTTAAAATTCTT[-/CTT]GCTGAATTGATTGTT | 57626 |
rs79706319 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038186 | GAGATTTTATAGTTT[C/T]CACTCAGCATTATGC | 57626 |
rs79713224 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023759 | ATGGTTGTTTTCTAG[A/C]TTTCTAGCTTGTTTG | 57626 |
rs79739358 | snp | G/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728923 | GATTCTTAAGGGGGT[G/T]GTACTACATATTTAT | 57626 |
rs79751975 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055762 | AGTTTAAAATGGAGT[A/G]TAATATTTTGTTTGC | 57626 |
rs79771363 | snp | C/T | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079682 | TGCTGTTATCAGTGC[C/T]TTAAGCATATTAATT | 57626 |
rs79779586 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091494 | CTCTAAAAGAGTCCA[C/T]CCACATCACAAATTT | 57626 |
rs79781802 | snp | C/T | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825858 | AGATAGAAATATTGC[C/T]GATAGGGTATATCCC | 57626 |
rs79783962 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027757 | AAACAAATGTTTATT[A/G]TTTTAAGCCTCTGAG | 57626 |
rs79790092 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750935 | ATTGAACTGGGATGA[C/G]GTCCAGACACAGAGA | 57626 |
rs79793887 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69945711 | CAAACACAATGACAT[G/T]CCACAACACCTCTAT | 57626 |
rs79798521 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917199 | GTAGAGTTATCTGTA[C/T]ATTCTTCTATGCCGT | 57626 |
rs79803144 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004700 | TCTGCATTAAAAATA[C/T]TTTTTTAAAATGTTG | 57626 |
rs79819452 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69917783 | GTATCACATAACATT[C/G]CACGTATCTTTTGAA | 57626 |
rs79821356 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100410 | CTACATTTTTTTGTC[A/G]ATTTCATCAATTTTT | 57626 |
rs79835517 | snp | A/C/T | 0.0256215 | 0.110247 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079315 | AATCTCCCAGCATGG[A/C/T]ATTTACCAATTGTTA | 57626 |
rs79836033 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790022 | GAGATGTAATTGTGG[G/T]CTCTATTTAACTATC | 57626 |
rs79852190 | in-del | -/GTTAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855914 | TTATATATATTATAT[-/GTTAT]AACATATTAATATGC | 57626 |
rs79868856 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948600 | AATCTTCCAAATATG[A/T]ATGAGTAGACTTAAA | 57626 |
rs79882494 | snp | C/G | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804910 | AAAATTTTTTATGAT[C/G]CATAACACATAAGAC | 57626 |
rs79883250 | snp | A/G | 0.361053 | 0.22398 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739647 | AAGATCATAAAAGAC[A/G]AGTCCTTGAAGAGGA | 57626 |
rs79886976 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877810 | GCTCCTTTTGTCTAC[A/G]CTGCTCTTATCTGAA | 57626 |
rs79888543 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949837 | AACAGTTAACAATGA[A/C]ATTTAAATTTTACTG | 57626 |
rs79894413 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730238 | CTAATTATCCAAAAA[A/T]TATGGATAAGTAATG | 57626 |
rs79899610 | snp | A/T | 0.117305 | 0.211877 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707591 | TGAAATAAATTCTTA[A/T]CCTTGAAGTGAATTA | 57626 |
rs79937852 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750514 | TACATGTATGTGTGT[A/G]TATATATGCATGTGT | 57626 |
rs79948399 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819630 | TGCAAAAAAAAAAAA[A/T]TGTAGAAATAAAAGA | 57626 |
rs79957680 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725040 | ACATCCAAGGGATCT[C/T]TGAGTTTTGGAAACT | 57626 |
rs79961354 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850921 | TCTTCTTTTGAACTA[C/T]CTGACTGACTCCTAG | 57626 |
rs79961809 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079910 | AGTGAAGAGTTTTTT[A/G]GAACTGAATCATTTT | 57626 |
rs79974618 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056483 | CTGCATTATAGACCA[A/G]ATGGAACTAATGTAT | 57626 |
rs79983361 | snp | A/G | 0.151001 | 0.229563 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720488 | CATGCACTCAATTCT[A/G]CTGAAACAGGGATAG | 57626 |
rs79996057 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818911 | TTATTATATTGCTTT[C/T]CTTCAGAAAAAGTCA | 57626 |
rs79998787 | in-del | -/A | 0.219947 | 0.248187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070543 | ACATTAAGGAAAAAT[-/A]AAAAAATTCTTAAAC | 57626 |
rs80006796 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901867 | CAATGGCGCCATCTT[G/T]GCTCAATGCAACCTC | 57626 |
rs80015632 | snp | C/G | 0.32627 | 0.238082 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945291 | ATAAAACTTCCATAA[C/G]CAAACTTTGTTAATT | 57626 |
rs80023219 | snp | A/T | 0.237303 | 0.249677 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981792 | AAAAAGTGCCCAAAA[A/T]AAAAAAAAATCTAAA | 57626 |
rs80032158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894961 | TTGTCTACAAATGAC[A/G]GAATGCTGATGTAGT | 57626 |
rs80052340 | snp | C/T | 0.16976 | 0.236773 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962765 | ATTTTCCTGATCTGA[C/T]TTTTAATCAAGGCTA | 57626 |
rs80058095 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70002731 | CCATTAAAATAACTC[G/T]AGTCACTACTTGATG | 57626 |
rs80075776 | snp | C/G | 0.0718919 | 0.175435 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991326 | GAACTGAAGAATATA[C/G]AGACACACAAAAAAA | 57626 |
rs80088474 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817320 | TGTATGGCAAAAAAA[G/T]AAGTCATAAAATGTC | 57626 |
rs80093360 | snp | A/C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723544 | AATAAAATTCTAAGG[A/C/T]TCCCAATGATATGAA | 57626 |
rs80095051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771686 | TACTAACGGTGAAGA[C/T]ATGTGGGTGCATAGT | 57626 |
rs80095526 | snp | A/C | 0.0821764 | 0.185298 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798022 | GCTAAATTACTGGTG[A/C]GATTTGTTTTAATGG | 57626 |
rs80120512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794544 | AAAGGATGAACAACA[C/G]AGAAAGAGGAGAGAG | 57626 |
rs80121148 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827766 | AAGTTATTCTTAGCA[C/T]ATCTCATCATTAACA | 57626 |
rs80142971 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69825997 | ACTTACAGAAAAAAA[-/AA]GATTTATTTATTTTG | 57626 |
rs80147514 | snp | A/G | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858076 | AAGGGCAGAGGCCAC[A/G]CCCTAAGGTCAGTTC | 57626 |
rs80150855 | snp | G/T | 0.0498117 | 0.149749 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834103 | GGATGAAAGAGTGGA[G/T]GTTGAGGGACAAAAG | 57626 |
rs80152643 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930894 | TTATGCATATATGCG[A/T]TAATCAGTGACTACA | 57626 |
rs80165953 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704212 | AACAAAATGTGATAT[C/T]CCCCTTGTGTTTCTT | 57626 |
rs80178445 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865605 | ATTTACATGGAGTCC[A/G]TTGCATAAAAATGAT | 57626 |
rs80179954 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910751 | TAAAAAGATAAAATC[A/C]TGACACTCATACAAA | 57626 |
rs80188365 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977340 | AATTTCAAGTCATAT[A/G]AAAAAAATCAAATGG | 57626 |
rs80191227 | snp | A/C | 0.0558544 | 0.157504 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097340 | AACTTCTTTTCTTTG[A/C]GCAGTATAATTTGTC | 57626 |
rs80198594 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877037 | AGCATAACTCTGTCC[A/C]AAAAAAAAAAGATAT | 57626 |
rs80203347 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077644 | ATAAGTGTACTATAT[A/C]AAAATGATGTGTTAA | 57626 |
rs80203935 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101064 | CTGAGGATACATAAA[G/T]TATCTTTGGAGACTT | 57626 |
rs80209375 | snp | A/C/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779226 | GGAATACCTAACTTA[A/C/T]GAATTCAAAAGGCCA | 57626 |
rs80210539 | snp | A/C | 0.0685596 | 0.171987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027046 | CAATGGGAAACAACA[A/C]ATTTTGAGTTTAGAG | 57626 |
rs80216038 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789746 | GAGCTACTTCTCCTT[C/T]CTCACCTTGAAAACG | 57626 |
rs80216399 | snp | A/T | 0.0952156 | 0.196321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768341 | TGAAATTATTACATT[A/T]CACAAAGCTTCTACA | 57626 |
rs80219628 | snp | C/T | 0.264632 | 0.249571 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988305 | GACCTCATTCTTTTT[C/T]ATGGTTGCATACTAT | 57626 |
rs80247102 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855347 | ATAGATAGATAGATA[C/G]ACAGACAGATAGATA | 57626 |
rs80280347 | snp | A/G | 0.119978 | 0.213528 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864998 | GCTGTCCAGGCAGGA[A/G]TGCAGTGGTGTGATC | 57626 |
rs80284649 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916761 | TAATAAAATAAAGTG[A/G]AAAAAAAACCACATA | 57626 |
rs80291378 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946674 | TGCACCACTAGGTTC[A/G]GCTATTTATTTTTAT | 57626 |
rs80291493 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998439 | GAGAATGGGGACTAG[A/G]AATCAACTGTGACCC | 57626 |
rs80299813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948973 | ATTCAAACCTCAAAA[C/T]TGACATTTTTARTAA | 57626 |
rs80302323 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857614 | TCATTTGTATATGCT[C/T]AGTCAGAAAGGAATA | 57626 |
rs80325842 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039059 | TATCCTTTGCACATT[A/T]TTTTTTTTTTTTTTT | 57626 |
rs80348453 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731358 | AACAAAATATTTTAA[C/G/T]TCCTTCTAGAAGTCT | 57626 |
rs111229477 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920240 | TTCACTAAAATACAT[A/G]TGAGATTGTCAGTTT | 57626 |
rs111237638 | snp | A/C | 0.0839998 | 0.186933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896431 | TGAATAATCAGGACA[A/C]CTTGGCAGACGGGAG | 57626 |
rs111238126 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783428 | GTTAAATACTGTGAA[C/T]AAAAAATTAGACAAA | 57626 |
rs111242830 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873883 | GACCTCTACATCTGT[A/G]TTTCTCAAAAATATA | 57626 |
rs111254002 | snp | C/T | 0.444444 | 0.157135 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859604 | TACATCAGGTTGCAA[C/T]GTGAATGAATTATTG | 57626 |
rs111265558 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780349 | TTGTGAAAACTTACA[A/G]AACTTTGAAGAGAGA | 57626 |
rs111271131 | in-del | -/ACAAAGGC | 0.262159 | 0.249704 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983909 | TACGGCTGATTTTTG[-/ACAAAGGC]ACAAAGATCCCACAG | 57626 |
rs111285218 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930880 | TTATGTATGTAAATT[C/T]ATGCATATATGCGTT | 57626 |
rs111289446 | in-del | -/A | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065885 | ATCAAAACCAAGATG[-/A]AAAAAAAAAACTATT | 57626 |
rs111298813 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870585 | AACTCAAAAGTCAAG[C/T]CTCATTTGAGACTCA | 57626 |
rs111301822 | in-del | -/T | 0.039522 | 0.134904 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932283 | TATTATAAAGGGGGA[-/T]TTTTTGTATGTATAA | 57626 |
rs111307980 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740300 | AAAATGTTTTAAAAC[A/C]ATTTTTACCAGCTTA | 57626 |
rs111312169 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067334 | CCTGTGAGGTAGGTA[C/T]TATTTTTTACTATTC | 57626 |
rs111319403 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785094 | AGACGGGGTTTCACC[A/G]TTTTAGCCGGGATGG | 57626 |
rs111321062 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932825 | CCAATTTGTAACACG[A/T]GTACAAATTGCCTGT | 57626 |
rs111322942 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802663 | TCCAATCTAATTACC[A/G]GTGCATGCAGCCCCC | 57626 |
rs111324959 | snp | C/G | 0.00153492 | 0.0276605 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107517 | GCTCACACCGCTTCT[C/G]TCTTGGCTTTTGAGC | 57626 |
rs111334301 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913691 | GGAATGGATTGCTTG[C/T]TCAATGAAATTCAAT | 57626 |
rs111395379 | snp | C/T | 0.5 | 0 | missense | KLHL1 | GRCh38.p7 | 13:69796896 | AACTGCAGCCTTCTG[C/T]CATTCATCATCCCTG | 57626 |
rs111396501 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766737 | AAAATGGATTAGATT[A/C]TCTTAATGATATTTT | 57626 |
rs111398190 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865588 | GTCACAGGAGTTTGG[A/C]AATTTACATGGAGTC | 57626 |
rs111398249 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727898 | ACCTCAGCCAAGTTA[A/C]TATATGATCTCTTTG | 57626 |
rs111409150 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813481 | ATATATACACACACA[C/T]ACACACACACACACA | 57626 |
rs111418432 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077508 | TGAAATTATTATGTA[C/T]GATCCTAAAATAATA | 57626 |
rs111423411 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715544 | TTTTTTTTTTGAGAC[A/G]GAATCTCGCTCTGTT | 57626 |
rs111433673 | snp | A/G | 0.148661 | 0.22854 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075182 | ATAGGGAAGAGATGT[A/G]TGGATTTGGGAGGCA | 57626 |
rs111439942 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869773 | TTTAACCTACTTGTG[A/G]TCCCATCACATGGCT | 57626 |
rs111444961 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107583 | GCCACTGCCGTCCTG[C/T]TGCAGGCAGCCTCCC | 57626 |
rs111448581 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930965 | GCTCAACTGCAATAT[A/G]TAATATTTACTTGTA | 57626 |
rs111451452 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022672 | TCCTTGATTTCTTAT[A/G]TATGGAAATCAGTGG | 57626 |
rs111470171 | in-del | -/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816428 | GCCACGCCTGGCTAA[-/T]TTTTTTTTTTCCTTT | 57626 |
rs111478710 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737570 | GCCAGCAAGACTGGG[C/T]GGTCTGGACTGGGAG | 57626 |
rs111479974 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69969941 | AATCGATTAAACTTT[G/T]TAAGTTCCACTTCAA | 57626 |
rs111482548 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877456 | TCAGGTATCCTCTAA[A/G]TAAACTATATATATA | 57626 |
rs111482567 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038284 | TGTGGTAGCAATGTA[C/T]TATGGCTTTTTAATA | 57626 |
rs111484412 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885985 | TAATCAGGGAGTATA[A/G]TATGTGATGCCATAG | 57626 |
rs111486246 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769375 | GAGTGGCAGAGTTTA[G/T]GATAGCATAAAAGGC | 57626 |
rs111487779 | in-del | -/TTTGGG | 0.459004 | 0.137176 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061391 | AAAATTTTCTTTTAT[-/TTTGGG]TTTAAGTGGTTTTTA | 57626 |
rs111499734 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075417 | AACATAATTTTCTGT[A/G]TAGAAAATTCCCACA | 57626 |
rs111505400 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69784881 | AATCAACAGAATATA[A/C]ATTTTTTTTTTTTTT | 57626 |
rs111508114 | snp | C/T | 0.401392 | 0.198948 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785765 | AGACTGCTAGCAAGA[C/T]TAATAAAGAAGAAAA | 57626 |
rs111543508 | in-del | -/AT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736691 | GAGATATATATATGT[-/AT]ATATATATATACACA | 57626 |
rs111574350 | in-del | -/CTTC/CTTCCTTC | 0.502025 | 0.211058 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779328 | TCTGTTAAAAAAGGT[-/CTTC/CTTCCTTC]CTTCCTTCCTTCCTT | 57626 |
rs111575544 | snp | A/G | 0.0158469 | 0.0875917 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107931 | GGACCTGGGCGTGGG[A/G]ACACCACCAGGCAGG | 57626 |
rs111596556 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718708 | CCAAAGAGAACTCAG[C/T]GATACCTGTGCCAGA | 57626 |
rs111615081 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897085 | ATCTAGTCAACCGAA[A/C]CCCTTGAAAGGATAC | 57626 |
rs111654521 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798704 | ACATAGTTGAATAAC[C/T]TCAAAGTCATCTGGA | 57626 |
rs111658856 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044974 | TAACCTTCTATGACC[A/G]AGTTATCTTGTCATG | 57626 |
rs111665309 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005184 | AGAGAGAAAATAAAC[A/C]TTTATATCTAAAATG | 57626 |
rs111676179 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852250 | ACTCCATCCGGAATA[G/T]GTAATGGCCTCACGT | 57626 |
rs111685474 | snp | C/T | 0.448708 | 0.151707 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978576 | ACTGCAACCTCTGCC[C/T]CCCGGGTTCAAGTGA | 57626 |
rs111693003 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711113 | AGTGTCATTTTCATA[C/T]TTTAAGGATAATAAT | 57626 |
rs111699725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885895 | GTGGACCTAAAATAT[C/T]AGAAAGGAGTTTAAA | 57626 |
rs111704312 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839567 | CAAGCTTACTGTAAG[C/T]GTTCATATATTTAAT | 57626 |
rs111713541 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990452 | AATGACATGCATAAT[C/T]TCAAAATAAAGGGAT | 57626 |
rs111716516 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002512 | AGTCCCAGGAGGCAA[G/T]GTGAGAGGGAAGGGG | 57626 |
rs111722848 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715525 | GCAGTTTTATTATTT[-/A]TTTTTTTTTTTTTGA | 57626 |
rs111732366 | in-del | -/AAAT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799633 | TTCCAATTTAGTGAC[-/AAAT]AACACAGATTTGTTA | 57626 |
rs111739473 | snp | A/T | 0.00557542 | 0.0525036 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701249 | ACCACATATGATTAG[A/T]AAAACAGTAAACCAA | 57626 |
rs111749350 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042807 | AGGCATTGCTATCCT[A/G]GGAGATGACAGCTCC | 57626 |
rs111757498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756369 | TTTTGTGACTAAAAT[G/T]AATTTCTGATCAATA | 57626 |
rs111764984 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746087 | CCTATGCTATTGCAA[C/T]TGGCATTTTTAAATT | 57626 |
rs111774118 | in-del | -/G | 0.0678174 | 0.1712 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039242 | CCCAGCTAATTTTTT[-/G]TTTGTTTGTTTGTTT | 57626 |
rs111790734 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926332 | ATTAAATGCCATGAC[-/T]TTTAAAAAAAATAAA | 57626 |
rs111798646 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763113 | GTGTCCCTCATAAAA[A/T]GTTCTATAGCAGATT | 57626 |
rs111812228 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956750 | TTGAATATATAACTG[C/T]GTCCTCATATTAATT | 57626 |
rs111818515 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69702918 | CACATCTTGTACTGT[A/T]ATCTCCATGAGAGAG | 57626 |
rs111828873 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903515 | CTTTCTTCGTTCTAG[C/T]TCTCTAGAAAGCACT | 57626 |
rs111832444 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70016577 | GTGCTGGCATGCCAG[A/C]CTCCTTCTGTTTCAG | 57626 |
rs111855297 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058672 | TCAACATGATTCCTA[A/T]AAAATACCAATGATA | 57626 |
rs111862061 | in-del | -/TG | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816216 | TAGGACAGCTGTGTG[-/TG]AATGCAATTAATATA | 57626 |
rs111883192 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060851 | AAAAGAAAAAAAAAA[-/A]TGTGGTATATATAAA | 57626 |
rs111904783 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735240 | CTGCCTTTAACCTTA[A/G]TCAATATATGTATCT | 57626 |
rs111907404 | snp | A/C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748672 | CATCTTTAAAGAGTA[A/C/T]ATAACTCATAGTATT | 57626 |
rs111910043 | snp | A/G | 0.5 | 0 | missense | KLHL1 | GRCh38.p7 | 13:69940186 | GAAGCTGAAGAAGGC[A/G]CGCTGCAGCAAGAAG | 57626 |
rs111910116 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779891 | TCTCGGCTCACTGCA[A/G]CCTCCACCTGCCAGG | 57626 |
rs111912058 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835392 | CAGTGAGGTGAAACC[A/G]GAGAGAGAGCTAAAG | 57626 |
rs111913771 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763515 | TAGAATATCAAATGC[A/G]CTCTCTTTGACTGAG | 57626 |
rs111914147 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978939 | ATAGAAAGAAATAGA[A/C]AAGAAAGAAATAGAG | 57626 |
rs111915794 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956332 | GGCATAGTACATAGT[A/G]GACATACATATAGTA | 57626 |
rs111918967 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099063 | AAGAACACAGAAAAC[A/G]GTCTTATAATTTTCT | 57626 |
rs111927885 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066152 | CCTGTGGTTTACCAG[C/T]TGTGCTTTTTACTGT | 57626 |
rs111931994 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776663 | GGAATATTTACATGC[A/C]CATGCAGGTTAAAGG | 57626 |
rs111947180 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015952 | TTGACTACATTTCTA[A/T]GGGGTAGACCCTTAA | 57626 |
rs111956856 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817887 | ACAGTCTTCATTCCT[A/G]GAAAGACCTACAGAA | 57626 |
rs111983502 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734407 | TCGGGTATTTCTTTA[C/T]AGCAATGTGAGAATG | 57626 |
rs111992464 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025834 | CGTAAACCACCTCTG[A/T]TCATCTTTATGCCTA | 57626 |
rs111994144 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845864 | TTACTGCTTCAAGAT[C/G]CTATGGGCTCAGAGA | 57626 |
rs111999997 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799516 | TTCAAAAGTGACCTA[C/T]TCACTTATCCTAGTA | 57626 |
rs112000514 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714977 | TCCTTCTTCCTCAAA[A/G]CATGCAGATAAATTA | 57626 |
rs112009494 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977106 | TATATTTAGGAAAAG[A/G]CATTCTTATATGGAC | 57626 |
rs112015474 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69977728 | TATTGAACCTCTTCC[C/T]CTTGAGATGCAGAAC | 57626 |
rs112020045 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078449 | ATTTGTATAACTTCC[A/G]AATTTTCTCTTTAAA | 57626 |
rs112021072 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714912 | ATCCTTCTATCTATA[C/T]AGAATAATGCTTGTT | 57626 |
rs112024004 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805534 | GAAGTAGGTAAATCA[C/G]AAAAGCAGAATACAA | 57626 |
rs112025412 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070438 | ACCATGCAGGCAAAA[A/C]GAGAGTGGAGTAAAA | 57626 |
rs112026884 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923022 | ATTATTTAAAGAATT[A/T]GGTGGGAGGAGACAG | 57626 |
rs112032547 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708096 | TAACTATTATCCACA[A/G]TAGAATTAGGGTATT | 57626 |
rs112038205 | in-del | -/AC | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876652 | CATAAACACTCACAA[-/AC]ACACACACACATTGC | 57626 |
rs112039148 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939376 | ATATATATATATATA[C/T]ATACACACACACACG | 57626 |
rs112039483 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881382 | TTTAGTAACATATGG[A/G]TTAGTAAAAATGTTG | 57626 |
rs112079106 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959142 | TTTTGTATCCTGTCC[A/G]CCCTCTACAAGCAGA | 57626 |
rs112087643 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811532 | ACACCATACTGAATA[A/T]GCAGAAGCTTAAAGC | 57626 |
rs112095505 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010254 | AGTATCACTAGTGTT[A/T]TGTATAGAATAGATT | 57626 |
rs112096829 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992280 | TGATATTCTAGGACT[C/G]AAAGACCTAAAGATA | 57626 |
rs112106421 | in-del | -/A/AA | 0.398354 | 0.201224 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775995 | ATACAAAAAAAAAAA[-/A/AA]CTAGCTTGGCGTGGT | 57626 |
rs112107132 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818729 | AGTTTTGAGTTGTTT[C/G]TATAGCTGTGTGCAA | 57626 |
rs112110376 | snp | A/C | 0.444444 | 0.157135 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782574 | GATTGCTAGCATAGG[A/C]GTCTGAGATCAAACT | 57626 |
rs112132375 | in-del | -/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843812 | TGTGTTAGCTTAGAC[-/T]TTTTTTTTATACTTT | 57626 |
rs112153124 | snp | A/C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719217 | GTGTGTGTGAGAGAG[A/C/T]GAGAGAGAGAGAGAG | 57626 |
rs112155017 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009155 | TTTGTGTAAGTCACG[A/T]CTCCTTCTATTAATA | 57626 |
rs112157066 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736384 | TAATCCAAAGATTTA[A/G]AAAAAACAGATTTTG | 57626 |
rs112184771 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925614 | ACCATATCTATCTGA[A/T]ATTATATATTAATTT | 57626 |
rs112192472 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69895734 | TTTTTTTTCAAGGTC[C/T]TGCTCTGTCGCCCAA | 57626 |
rs112201018 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080323 | AGTGACCACAGGATC[A/G]TTTATACTTCCCCAA | 57626 |
rs112226925 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836149 | TAGAAATGATTGATT[C/T]ATAAGCAGCTCTAGG | 57626 |
rs112235467 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718901 | TGGTATGTCATAAAA[G/T]AACTTGATAATTCAC | 57626 |
rs112236995 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949194 | ACTTCCTTTACATTC[C/T]TTAGATTTTTTTTTC | 57626 |
rs112260364 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958739 | TCAAACCTTAAAATT[A/T]AAAAAAAAAAATACA | 57626 |
rs112263438 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884526 | CTAAAAAATCTATGC[C/T]TCCATTAAACCACAC | 57626 |
rs112268070 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083536 | TTATTAATTTTAGAC[G/T]TTGTAGATTAACTCT | 57626 |
rs112276751 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883385 | ATGACTTTTATCAAC[C/T]TTGCTTTTCTAAATT | 57626 |
rs112285647 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002730 | TCCATTAAAATAACT[C/T]GAGTCACTACTTGAT | 57626 |
rs112285917 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875085 | AGAACAAATTAGCAA[C/T]GACAGTTGAGCAAGA | 57626 |
rs112310236 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923913 | GGGCCTGGGAAGCCC[C/T]ACCCTGCCACCACAG | 57626 |
rs112333559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833033 | TAATTCTTCTGAACA[C/T]TGTCTTAGGCAAAGA | 57626 |
rs112334479 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817830 | TAATTATGGTAGGCC[G/T]TTTATCATAGCACAT | 57626 |
rs112343530 | snp | C/T | 0.326035 | 0.238157 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945054 | GCAGTGGCGCCATCT[C/T]GGATCACTGCAACCT | 57626 |
rs112352489 | in-del | -/TT | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712760 | TTTGTTTGTTTTTTG[-/TT]TTTTTTTTTTTTGGG | 57626 |
rs112358430 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785086 | TTTAGTAGAGACGGG[G/T]TTTCACCATTTTAGC | 57626 |
rs112361703 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827503 | TTGGGAAGCCAAGGC[A/G]GGTGGATCATGAGGT | 57626 |
rs112367560 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767270 | AAAAAAAATTAAAAA[C/T]ATGTACATAAATTTT | 57626 |
rs112370731 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876177 | AAATCAAATATAACG[C/T]ATAAATTTCTTGAGT | 57626 |
rs112371279 | snp | A/C | 0.0803491 | 0.183626 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935251 | ACTGGTGAACTTGGT[A/C]CATAGTTCACCTACT | 57626 |
rs112372097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893764 | CATTTTCATCCTGGA[G/T]GGTCTCAATTCTGGA | 57626 |
rs112373080 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851085 | ATACTTAGTAGTCAC[A/C]ACTGAAAAACATACA | 57626 |
rs112383195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889538 | CCCATCTATTTTGAG[C/T]TTAATGTCTTACTTT | 57626 |
rs112383324 | snp | A/G | 0.143622 | 0.226238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885096 | CAGGCGCCCGCCACC[A/G]CGCCCGGCTAATTTT | 57626 |
rs112386642 | in-del | -/TAA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805172 | TCTAAATCATTATAA[-/TAA]TTCCAAATGTGCCAA | 57626 |
rs112390105 | snp | A/T | 0.0737376 | 0.17729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807544 | CAAACCACACTCCCC[A/T]TGTAGTTCACCTGAG | 57626 |
rs112392266 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935305 | AATAGTCACTATACC[A/T]TCATTTATTCATTCA | 57626 |
rs112395185 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097274 | TATCAAGAATAGATT[A/T]TAAAATAAATAAAAC | 57626 |
rs112414923 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075743 | CATAGGTGTATATAT[A/G]TACACACATACACAC | 57626 |
rs112426311 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925980 | CAACAATAATCAAAT[A/G]CAATACATATGCATT | 57626 |
rs112438176 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765532 | AGGAAAAACTCTTAT[C/T]TTTAATTCCTACAAT | 57626 |
rs112442890 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816330 | CAGTAGCACAATCTC[A/G]GCTCACTGAAACCTC | 57626 |
rs112452652 | snp | A/G | 0.084364 | 0.187256 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878975 | ATGAAGCTGGAAACC[A/G]TCATTCTCAGCAAAC | 57626 |
rs112456063 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756384 | GAATTTCTGATCAAT[A/G]TTTTATTGATTCTTT | 57626 |
rs112457423 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068860 | TCAGTCTCGTCGTGG[A/G]GGAGGAGGCACACTT | 57626 |
rs112457670 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086572 | AGGGAAGCTCTGTCT[C/G]AAAAAAAAAAAAAAA | 57626 |
rs112468352 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961179 | AGTCTGATTTTTGAT[C/T]TACTAGTTTTCAACT | 57626 |
rs112484721 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783971 | GGGAAGCCCATCAGA[C/G/T]TAACAGCTGATCTCT | 57626 |
rs112487690 | snp | C/T | 0.444444 | 0.157135 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912853 | TGCTGGGAGACTACC[C/T]GCTTGCCTTCTGTGA | 57626 |
rs112488951 | snp | C/T | 0.5 | 0 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108225 | CAAGTCTCGAGGAAG[C/T]GTACCCCTCGCCAGA | 57626 |
rs112501952 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69977920 | AAATTCTATATCCAC[C/T]GATATTACCTGTGTT | 57626 |
rs112508820 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723895 | TTGCCCAGGCTGGAA[C/T]GCAGTGATCTTGGCT | 57626 |
rs112508877 | snp | A/C/T | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922361 | CAAAGTGGTGAAGTA[A/C/T]GAAATGGTGGAGAAC | 57626 |
rs112519135 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925089 | CTCACAGGCTGAGTG[A/G]GTCCAGCAGGTTCAA | 57626 |
rs112523039 | snp | A/C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70041133 | GCTCATTTTAAAAAA[A/C/T]TTTTTTTATTTGTAG | 57626 |
rs112525844 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039543 | ACAATCTTTTTCAAA[C/T]GGCAAAAGATTTATT | 57626 |
rs112540612 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766479 | TAATTTTTATATATA[C/T]ATACATATATATATA | 57626 |
rs112547018 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761692 | GCATTTAATAAATGT[G/T]CTATGCACTTTAATT | 57626 |
rs112557028 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101147 | AGCCAGATACCAATT[A/T]TGATTACATATGTAG | 57626 |
rs112560270 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875276 | CATATTATGTTGGAA[A/G]GGCAAAAGAGAGCTG | 57626 |
rs112564139 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815310 | AATCAACCCAGTTGC[C/T]GACCAATGGTTGATT | 57626 |
rs112579383 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890130 | TTATAAAATAATTAC[A/T]TTCATTTTATAATAA | 57626 |
rs112583185 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887367 | GTAAACCTTGACCAC[G/T]GCTTTGGTGTTCTCT | 57626 |
rs112597169 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711304 | TGTAAAACAAACAAA[A/C]AAAAACAAATTAAAA | 57626 |
rs112606117 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823019 | CAAAAGTTCGCTATC[A/G]AGAGCTTGCATTTTA | 57626 |
rs112607889 | snp | A/C | 0.0872718 | 0.189788 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996129 | CCAACATGGTAAAAC[A/C]CTGTCTCTACTAAAA | 57626 |
rs112614101 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950128 | TCTCAGAGTTCAAGA[A/G]AAACTGTTAGAAAAG | 57626 |
rs112615834 | snp | A/G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755837 | AAATAAAATGAAACA[A/G/T]GTGGGTAGTGGAAAA | 57626 |
rs112617712 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770357 | AAACTCATGCAGAAG[C/T]TTTGCTGGCCACGGA | 57626 |
rs112617747 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861880 | TGAGGCAGGAGAATT[G/T]CCTGAACCTGGGAGG | 57626 |
rs112619831 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772909 | GTTTGATTCAAGAGA[C/T]AGAGTTTTTTTTAAC | 57626 |
rs112627006 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790272 | CTGGAAACTAAAAAT[A/G]AGGCTGGGAACAATA | 57626 |
rs112632313 | snp | A/G | 0.444444 | 0.157135 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061080 | ACCACAGGCTGGGAG[A/G]GGTCACTGGGGGAGG | 57626 |
rs112638048 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729528 | AGGGGAAAAAATCAC[A/G]TCAGCAGAGGTGAGG | 57626 |
rs112652363 | in-del | -/A | 0.0792174 | 0.182574 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868417 | ATGACATGGACATAC[-/A]TTTTTTTAGATGATG | 57626 |
rs112665486 | in-del | -/AAAA | 0.465065 | 0.162525 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788670 | ATAATAATAATAATA[-/AAAA]GAAAATATAGTATTT | 57626 |
rs112667202 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101156 | CCAATTTTGATTACA[C/T]ATGTAGGCTTTCTTT | 57626 |
rs112669113 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078325 | ATATTAAATAGAATT[C/T]TCATCCACAAAAATA | 57626 |
rs112675712 | snp | C/T | 0.32627 | 0.238082 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945020 | AGATGGAGTCTCACT[C/T]TGTCGCCCAGGCTGG | 57626 |
rs112675958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895503 | TTGATTTGTATATTA[C/G]TTTCCTATTGCTGCT | 57626 |
rs112692826 | snp | C/G/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862592 | TTATACCTGTTGCTA[C/G/T]GTACTGAATTGTGTC | 57626 |
rs112697882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828546 | GGGTACAATCCAGGG[C/T]GGAGTGCAAATGGGA | 57626 |
rs112706128 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814943 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 57626 |
rs112709566 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983699 | TTGAGCCCAGGAGTT[A/C]AGAGTCGGCAATGAC | 57626 |
rs112717457 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800684 | CTATCTAAGCCACCT[A/C]ATTCTATAATTACTA | 57626 |
rs112717494 | in-del | -/A | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933816 | AAAAAAATACTTGAG[-/A]AAAAAAAATCACAAA | 57626 |
rs112718356 | in-del | -/TA | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861566 | ATATGTATATATATA[-/TA]CACACGCACATATAT | 57626 |
rs112720711 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810114 | GCAACACCTTACTGA[C/T]AGCATTAGACAGATT | 57626 |
rs112721538 | snp | G/T | 0.143284 | 0.226079 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885142 | AGACGGGGTTTCACC[G/T]TGTTAGCCAGGATGG | 57626 |
rs112723085 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054987 | GGAGGAGATAGAGAC[A/T]TAAATTGGGGTTAAA | 57626 |
rs112724395 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032118 | TATCTTAAAGGTTTA[C/T]TGTAAACATTTAAAA | 57626 |
rs112725136 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916280 | ATGCTGCTATAAAGA[C/T]ACATGCACACGTATG | 57626 |
rs112727572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861851 | ATGCTTGTAATCCTA[A/G]CTACTCAGGAGTCTG | 57626 |
rs112731155 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923781 | GGCTACATTTGCCAT[A/G]GAAGAGGCAGAAGCC | 57626 |
rs112735125 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69876815 | GGCCGAGGCGGGTGG[A/G]TCACCTGAGATCAGG | 57626 |
rs112748235 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102471 | TCACTGTCAATTTAA[A/G]AAGTCTATTTAAACA | 57626 |
rs112749885 | in-del | -/ATT | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801852 | CTACAATGCCCATTG[-/ATT]ATTTTCTTTTTATTA | 57626 |
rs112752534 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800330 | ATAACATATTCACAG[G/T]TTCCAGGGTTTAGGA | 57626 |
rs112753890 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811610 | TCTATTCAACACAAT[A/G]CTGGAAGTCCTGGCT | 57626 |
rs112767369 | snp | C/T | 3.3206e-05 | 0.00407455 | missense | KLHL1 | GRCh38.p7 | 13:69961422 | TGGCCGCAAAATAGT[C/T]GGAGACTGAACTCAG | 57626 |
rs112787623 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006238 | TGTTGTATGCATATA[C/T]GACATTTTCTTTATC | 57626 |
rs112797305 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780893 | TCATTGATTCTGTTT[C/T]CCTGACACATGAGCA | 57626 |
rs112806952 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976431 | AACTTTATGATTTTG[G/T]AAAGTCCATGATACT | 57626 |
rs112820895 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925044 | TTGGCAGGCATGGGA[C/T]TCAGGCTGGTAGTGC | 57626 |
rs112827339 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867210 | TATATTATAAAGTAT[C/T]TTAAGTATTTTGAGA | 57626 |
rs112827664 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779385 | CCCCTCCCCTCTCCT[A/C]CCCTGTCCTCCCCTC | 57626 |
rs112841604 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818454 | TCCATCTCTTGACCT[C/T]GTGATCCACCCACCT | 57626 |
rs112853591 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812010 | AGGGTGTCAATCTTA[A/G]ATCTTTCCTGCTTTC | 57626 |
rs112859443 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725904 | AGCCCTATGTAGCAT[A/G]GTGCATTCATATTTA | 57626 |
rs112864168 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936416 | CAACAAGGTGAAACC[C/T]CGTCTCTACTAAAAA | 57626 |
rs112891018 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857652 | CTTTCTATAAAAGAT[A/G]TATCATAAGTTGAAT | 57626 |
rs112901024 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749596 | AATTTTCATGTAACA[A/T]GGCACATGTTAAAAT | 57626 |
rs112916359 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69893317 | TCGGCTCACTGCAAG[C/T]TCCGCTTCCCGGGTT | 57626 |
rs112920871 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69861293 | TAGCCCTTCCCTCTT[C/T]AAATTCTCCACCTTT | 57626 |
rs112938169 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889390 | AGCTAAGAGGAGCTC[A/G]CATATAGTCATACTC | 57626 |
rs112959941 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964057 | TCAGTTTGTTTGTTT[G/T]TTTAAAAATAGGCTC | 57626 |
rs112961743 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945480 | AAAAAAAAAGCCACT[A/G]TAAGATATATTATTA | 57626 |
rs112977423 | snp | C/T | 0.264084 | 0.249603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984866 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGTGG | 57626 |
rs112983693 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937521 | CCAGAATTAAGCACA[A/G]ATTTCATAATATAAT | 57626 |
rs112986369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877135 | TGATAAAACTGAATT[C/T]CCCTGAGCACCTTTT | 57626 |
rs112990340 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814030 | ACCAAAACAGCATGG[A/C]ACTAGTAAAATATAA | 57626 |
rs112991777 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068290 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 57626 |
rs113014298 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890440 | TGTGCACTGATTACC[C/T]GGTAATTATTTTCAG | 57626 |
rs113023634 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886163 | CATGAACACACACAT[A/G]CATACACACATTTTC | 57626 |
rs113026904 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718685 | AATAGTTCTAAGTAA[C/T]GCACAGCCCAAAGAG | 57626 |
rs113027024 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827894 | AAAGTTTCTTAATCT[C/T]TTCAAATTCAAAATG | 57626 |
rs113031102 | in-del | -/GA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785596 | AGATCACAATTAAAA[-/GA]ACTAGAAAAGCAAGA | 57626 |
rs113033588 | snp | A/G | 0.189261 | 0.242509 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968808 | CACATTTTCTTAATC[A/G]AGCCTATCATTGTTG | 57626 |
rs113033795 | snp | A/C | 0.0839998 | 0.186933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895232 | GTTGCAGTTTGCTGG[A/C]AGCATCTGGTCCCTT | 57626 |
rs113037512 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808243 | GCTTCTTTAGCAGCT[C/T]TGCCATGACTACAGG | 57626 |
rs113051230 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841458 | CAAGTAGTCCATTTT[A/C]TTTACAGTGACTAAA | 57626 |
rs113055780 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720613 | ACTGGTGAGGGTAGA[G/T]ATTGTGGATACAATT | 57626 |
rs113060568 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760620 | TCAGACTCCCAAACT[A/G]CTGGGATTACAGGCA | 57626 |
rs113070285 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847419 | CAAAAAAAAAAAAAA[A/T]AAAAAAAACATAATT | 57626 |
rs113070289 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719215 | ACGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 57626 |
rs113073241 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716287 | TCTTAGTGTCTGACT[C/G]ATTCAATACATTCTT | 57626 |
rs113080092 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731081 | ATAAATAGAAAAAGT[A/G]GTATTAATAAATGTA | 57626 |
rs113090972 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027530 | TTGCATTTCATACAG[A/C]AAAGGGGGAGAAAAC | 57626 |
rs113095978 | snp | A/C | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047057 | TTGAGATAATACAAC[A/C]AAACCAACCAAACCT | 57626 |
rs113096893 | in-del | -/GTTCA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796615 | ATGTTAATTACCCAG[-/GTTCA]GGTATTCCTTTATCG | 57626 |
rs113097542 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057802 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 57626 |
rs113099721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894163 | GTGTTACTTTTATTC[C/T]ATGTTCTCTTATGGC | 57626 |
rs113102771 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776017 | AAAAACTAGCTTGGC[A/C/G]TGGTGGTGGGTGCTT | 57626 |
rs113104245 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939947 | GAAAACTCATTTTAA[A/G]CTTAAAAAACTTGCT | 57626 |
rs113110978 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868495 | TAAATTTAAATGAAA[C/G]ATTTATGGATTATTA | 57626 |
rs113112947 | snp | A/C/G | 1.65119e-05 | 0.00287327 | missense | KLHL1 | GRCh38.p7 | 13:69882447 | TATGGAGCTCCTCAG[A/C/G]TGGAAGGAGTAAAAA | 57626 |
rs113128263 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109341 | AAGGCAAAGGGACCA[G/T]AAATGCAATGTGTTC | 57626 |
rs113132596 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088397 | CAAATATAAAAAAAA[A/G]GGCCAGGTGTGGTGG | 57626 |
rs113141686 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707916 | TTTTTTTTCTCTAAA[A/G]GCTCAATCATTTGAG | 57626 |
rs113143454 | snp | A/T | 0.100231 | 0.200173 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060550 | AGACAAAAAAAAAAA[A/T]GTGGTATATATAGGC | 57626 |
rs113153421 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730775 | TGTAGAGATGGGGTC[A/T]CACTACGTTGCCCAG | 57626 |
rs113156975 | in-del | -/C | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913856 | GAAGGATGCAAAGTA[-/C]TTTTCCTGGGTGTGT | 57626 |
rs113158756 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886868 | TAAGCATTATAGTAG[A/G]AAGATAAATCCTTTG | 57626 |
rs113162248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907746 | TGATATCACAGAGAA[C/T]GGGAAACCAATTCAC | 57626 |
rs113174583 | snp | G/T | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832739 | CACCAAAACAGCATG[G/T]TACTGGTATAAAAAT | 57626 |
rs113185753 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733254 | AATCACTGAACTTAC[A/G]TATCTCCCCCACTCC | 57626 |
rs113191737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080148 | GAGTCTGAAAGGATA[C/T]GTGTTGGCATGAATC | 57626 |
rs113193781 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750879 | GAAATCACCTGGGAA[C/T]CTTTGAAAAAATACA | 57626 |
rs113220394 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879211 | AAGTATAATAAAAAA[A/T]ATATATATAAAAGAA | 57626 |
rs113224076 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830188 | ACCAACCAAGTATCT[A/G]CTATCTTCAAGAGAC | 57626 |
rs113230792 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750436 | ATTAAGGAAAGAAAT[C/G]GATAAGTAAAATTAT | 57626 |
rs113240254 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040046 | CTTATGCCAACATTT[C/T]ACCAGTTGTAATGAA | 57626 |
rs113252418 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012783 | AGGCATGGTGGTGGG[C/T]GCCTGTAGTCCTGGG | 57626 |
rs113270278 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718411 | ATGATCAATATTCTA[A/G]GTTTTTTTTTCATTT | 57626 |
rs113278656 | in-del | -/TAATAGTAGC | 0.0799831 | 0.183287 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725648 | ACCAGCTATGTGTTA[-/TAATAGTAGC]AAGTGTCAAGAGGAT | 57626 |
rs113281714 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69787967 | ATGAGATACCATCTC[A/C]CACCAGTTAGTTAGA | 57626 |
rs113307744 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777056 | TGATAAATTGAATCA[C/T]GGGGTGGGTATTTCC | 57626 |
rs113310002 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104036 | AAACATGACATGTCT[A/T]CTCCCACTCACATCA | 57626 |
rs113320423 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718455 | GGTAATATCATGGAT[A/T]TGTAGCATGAATGAG | 57626 |
rs113329313 | in-del | -/A | 0.459574 | 0.136304 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792587 | AACATATGTTCAAAC[-/A]AAAAGGCATATATAG | 57626 |
rs113333062 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69788181 | TACCCAAAGGATTAT[A/G]AATCATGCTGCTATA | 57626 |
rs113336251 | snp | C/T | 0.095934 | 0.196885 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935426 | GATAGACAACAAAAA[C/T]AACAATAACAAAAAC | 57626 |
rs113342336 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983468 | ATACTGTGCTCGGTG[C/T]GGTGGTTCCCACCTG | 57626 |
rs113347424 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833766 | ATATATATATATATA[C/T]ACATACATACATACA | 57626 |
rs113368313 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810515 | ACAACATTCCACAAC[A/C]TCTGAGGTGCGGCAA | 57626 |
rs113379854 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967722 | AACCCCGTCTCTACT[-/A]AAAAATACAAAAATT | 57626 |
rs113386100 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759791 | TGAGACTTCATGCCT[A/T]AATATTGTATCGTCA | 57626 |
rs113389608 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034045 | ACTTCCCTAAATAGA[A/G]TCAAAAAATAACACT | 57626 |
rs113390517 | snp | A/G | 0.084364 | 0.187256 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900141 | GAATACTCTGGATAT[A/G]GGTTTGCCTCTATGC | 57626 |
rs113394726 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950903 | AGTTCTATAATTCGT[A/T]GTTATATCCACTTTT | 57626 |
rs113401889 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932504 | TGATTGAAATCATTA[A/C]ATATTTAGGCACTAC | 57626 |
rs113404358 | in-del | -/GC | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071563 | TCACCAAGACACATC[-/GC]ACATTGCAGGCCATA | 57626 |
rs113410692 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014522 | GACAGTTAAGAAAAT[A/C]ATCACTGAGTCTGTC | 57626 |
rs113414914 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706262 | TTCCCCTTCTTTTCT[C/T]TACTCCTTCTTTTTA | 57626 |
rs113420251 | in-del | -/A | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855306 | GATAGATAGATAGAT[-/A]GATAGATAGATAGAT | 57626 |
rs113421189 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867925 | AGTTAATGGGTGCAG[C/T]ACACCAACATGAAAC | 57626 |
rs113431726 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079331 | ATTTACCAATTGTTA[C/T]AGTTCAAAGTTCCCC | 57626 |
rs113449545 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990097 | TCATAAGCAAAGGAT[A/G]AATAAGATCCTTTAT | 57626 |
rs113449766 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037217 | CATTCTTGATAAAGT[A/T]TTGGTGGTGACAGTT | 57626 |
rs113455257 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971463 | TTATGGTTTAATTTC[C/T]CAGTTATTTCCAATA | 57626 |
rs113460291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814554 | AAAAAAAATCAACAA[A/G]TAAAGTTAAAAAGTG | 57626 |
rs113460319 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043062 | AGGCGTGAGCCACCA[C/T]GCCCAAGTAATTTTG | 57626 |
rs113462833 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869840 | TGTAAACTAATTTTA[C/G]ACAGTTTATTTAGTT | 57626 |
rs113464071 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902739 | GAAGGGGAACATCAC[A/G]TATCGGGGTCTGTTG | 57626 |
rs113484214 | snp | C/G | 0.140242 | 0.224618 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797796 | ATCGCGCCACTGCAC[C/G]CCAGCCTGGGTGACA | 57626 |
rs113487949 | in-del | -/ATTTATGA | 0.472241 | 0.114494 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751921 | AAATTAAGAGGATGT[-/ATTTATGA]ATTTCTTTGCTTACA | 57626 |
rs113492130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887108 | GTCTAATGTTTTGGG[A/T]CTAAGATTTTAAAAT | 57626 |
rs113493859 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919757 | TGGCTTTCTGTTCTA[C/T]ACTTGGCCCTGTCTC | 57626 |
rs113494699 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789618 | ATGAACAAATGACCA[-/T]TTTTTTTTCCTCTAC | 57626 |
rs113502302 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821014 | CGTGACCACTGTAGA[C/G]TGAAAGCAGCCACAG | 57626 |
rs113502996 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959553 | CTTTTTTCAGACTAC[G/T]CATTAAAAAAAAAAA | 57626 |
rs113510761 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795836 | TGTCATAATGACTTA[C/T]GGTGCCAGCGAATGT | 57626 |
rs113515547 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856235 | CTTCATTTCAAAGGG[C/T]AGGTATAGTCACTGC | 57626 |
rs113523630 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060539 | AGACAAAAAAAAAAA[-/A]TGTGGTATATATAGG | 57626 |
rs113524024 | snp | C/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082852 | AGCTGGAGCCAATAA[C/G]CTAAGCAAATTAGCA | 57626 |
rs113530152 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009906 | AATAATGCTAATCAA[C/T]AGAAAAAAATCTGGA | 57626 |
rs113541851 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764982 | TTTGAGACCAAGTCT[C/T]GCTTTGTCGCCCAGG | 57626 |
rs113545157 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904935 | TCTACAATAATAATA[A/T]GCCTTAATAAAATAA | 57626 |
rs113549421 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813471 | AAATACACACATATA[C/T]ACACACACATACACA | 57626 |
rs113555463 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973068 | GCACAAATGAGTTCA[C/G]AATTTTGATTATTTT | 57626 |
rs113566934 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713030 | AGATGAGATCTCACT[A/G]TGTCACCCAGTCTGG | 57626 |
rs113570983 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741018 | TACTTACAACAATGT[C/T]ACCTTAAAGCAATGT | 57626 |
rs113575596 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069996 | ACACGGTGAAACCCC[A/G]TCTCCACTAAAAACA | 57626 |
rs113597596 | snp | C/T | 0.460589 | 0.13473 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782341 | GTGCAGCGCACCGTG[C/T]GCTAGCCGAAGCAGG | 57626 |
rs113597752 | in-del | -/TT | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933920 | TATCAGGAATTCGAC[-/TT]AATATTATGGGCAAT | 57626 |
rs113602495 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809306 | TTGAAGGCAACTAAG[A/G]AAAAGGGTCATATTA | 57626 |
rs113602789 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796425 | ATTAGTTCCCTCAAG[A/T]GCTGGTTGTTAAAAA | 57626 |
rs113605508 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772620 | TGTTGATCAACACTA[A/G]TTCTCTAAAAAGTGT | 57626 |
rs113606724 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775813 | CTCCTTCCACGTCAC[A/G]GAAAGGGGCTCTCCC | 57626 |
rs113624660 | snp | C/T | 0.444533 | 0.157025 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978533 | ACTCTGTCGCCCAGG[C/T]TGGGGTGCAGTTGCA | 57626 |
rs113627108 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868407 | TTAGAGAAAAATGAC[A/G]TGGACATACATTTTT | 57626 |
rs113631596 | snp | A/C | 0.030278 | 0.119257 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077860 | AAAATCGAAGTCATG[A/C]AAAACCTCTGGATAT | 57626 |
rs113633162 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769947 | TGCTCCTGTTTGCCA[C/G]ACTATGGGAGTGAAC | 57626 |
rs113638796 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69903639 | CACATTCTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 57626 |
rs113673870 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092796 | CTACATGTGGTTGTT[G/T]TCATTTATATTTAGA | 57626 |
rs113676379 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937048 | CTAACCAAAAACCAT[C/T]TAGAGAAAGGATTGC | 57626 |
rs113688130 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961832 | TTTCTATTATGTTTT[A/G]TTTGCCTGTTCTTGT | 57626 |
rs113689612 | in-del | -/T | 0.0143137 | 0.0833785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961216 | ATACAGAATACAGAA[-/T]TTTTTTTAAAAAAGC | 57626 |
rs113693968 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896862 | TTTTTTAATAGAAAC[A/G]GGGTTTCACCATATT | 57626 |
rs113694243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883615 | AGACCCTGATTTATA[A/T]AACCTTGTATATCTA | 57626 |
rs113695796 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898847 | AGGATTCAATGCCAC[A/G]TGTGGCTTGTGAACG | 57626 |
rs113697289 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793022 | AAATTTAATTAACTT[C/T]ATGATATGTGAATTA | 57626 |
rs113703162 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966463 | ATTGACAATGTTCCT[A/G]GTTGCTCAAGAGCTC | 57626 |
rs113705983 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855622 | ATAAGGGGCTCTCCC[C/T]GCTACACTCAGCAAT | 57626 |
rs113709010 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726638 | TTATTAAAACATACC[A/C]AAATTTATGAAAAGA | 57626 |
rs113714004 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701663 | TATAAAAATAACCAC[C/T]CCAGCAAGTAAAATC | 57626 |
rs113723775 | snp | C/T | 0.039522 | 0.134904 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925187 | CCCATAACAGTATTA[C/T]GGTTAAAACTTCAGA | 57626 |
rs113725878 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078156 | GCTCCTCATGTCTGT[C/T]TAGCATGCTCTAATG | 57626 |
rs113728024 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779376 | TTCCTTCCTCCCCTC[C/T]CCTCTCCTCCCCTGT | 57626 |
rs113732656 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894288 | AGCGTAATCCTGCTT[A/G]TGCAAATCTGAAAGA | 57626 |
rs113735296 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818073 | TTTCTAGTGAAGATA[A/G]GGCTGTAAAAGAAAA | 57626 |
rs113736427 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964349 | ACCCAGACCATCTTG[C/T]TTGTTATAGAAAGCT | 57626 |
rs113763518 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903518 | TCTTCGTTCTAGTTC[C/T]CTAGAAAGCACTTTC | 57626 |
rs113784430 | in-del | -/TGTGTGTGTG | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751113 | CATGTCATGTGTGTA[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 57626 |
rs113792172 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958208 | CATTGCTGTCTCTCA[A/G]TGATACCAAGGCCAT | 57626 |
rs113796757 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900095 | CTTCAACCTTGGAGC[A/G]GGGCAGACATTTATA | 57626 |
rs113797157 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038602 | TTTTTTTTTTTTTTT[C/T]TTTGAGATAGAGTCT | 57626 |
rs113798971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918436 | AACTTTTATATGCAC[C/T]GTTTATTTTTTCCTG | 57626 |
rs113801002 | in-del | -/TAAAA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815021 | CTCTAAAAAAATAAA[-/TAAAA]TAAAATAAAATAAAA | 57626 |
rs113807045 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976117 | TAAATTATTTACATG[C/T]CTATTCTAAAATTAA | 57626 |
rs113811614 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046444 | GACTTGGACCCAGGT[G/T]CATCTCACTTCATGG | 57626 |
rs113821506 | in-del | -/AT/TA | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997683 | TATATAATATTACTT[-/AT/TA]ATATATATAATATAA | 57626 |
rs113838024 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742794 | TGAGTGCAGGCATAG[C/T]TAAAATTAAAAACCA | 57626 |
rs113840323 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829335 | GCTAGACCCAGAAGA[A/G]CAAAAACAATCACTG | 57626 |
rs113847240 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035700 | GGTAATCTAGCAGCA[A/G]GAGCACATGTGCCTG | 57626 |
rs113849307 | snp | A/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892296 | AATCATGAGACAATA[A/T]CACACCTATGTGTTG | 57626 |
rs113862200 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923148 | GGAAGAAGGTTCATC[A/G]AATGGTAAAACAGAA | 57626 |
rs113873415 | snp | G/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755838 | AATAAAATGAAACAT[G/T]TGGGTAGTGGAAAAA | 57626 |
rs113875365 | in-del | -/TA | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773882 | ATATATATATATATA[-/TA]CATAGAATAAAACGT | 57626 |
rs113892645 | in-del | -/T/TT | 0.362104 | 0.223456 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895713 | TTCTTTCTTTTTTCC[-/T/TT]TTTTTTTTTTTTTCA | 57626 |
rs113900323 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69814330 | TCTTCTAGACATTTG[C/G]CAATAATTGGCAAAT | 57626 |
rs113902680 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808330 | CACTACCTACTGTCT[A/C]TTACTCTTAAGGACC | 57626 |
rs113910809 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791566 | AAACAAGAAAATGTG[A/G]GAATGGCATAAAGAT | 57626 |
rs113919327 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995253 | AAAAGTTTGGTGGTT[C/T]CTGTTATGATTCCAA | 57626 |
rs113931565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895323 | GTGTTAGGATTCTTG[A/C]CTCCTCCAGTATCAT | 57626 |
rs113945206 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69876283 | TTATAAATCAGATGT[A/T]TTAGTTGTAGCTATA | 57626 |
rs113952202 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008042 | GATCTATTTTGATGA[C/T]TGGCTCTTACTATTT | 57626 |
rs113954488 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711651 | TTTATAACTGCATAA[C/T]GGTAATAATGTTCCT | 57626 |
rs113958420 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955085 | CATCTAGTAAAAGCC[G/T]TAAGTTTAAAACTAA | 57626 |
rs113958646 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816483 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGCCCTGA | 57626 |
rs113962649 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901965 | ACCTTGCTCAGCTAA[A/T]TTTTTTGTATTGTTA | 57626 |
rs113967391 | in-del | -/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811408 | AGATAAAAAAAAAAA[-/G]CATTAGATAAAATTC | 57626 |
rs113997946 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827656 | AATCTCGTGAACCCC[A/G]GGAGTCAGAGGTTTC | 57626 |
rs114003307 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781707 | AAACACATAAAATCC[A/G]TTTTTTTGTCACTCA | 57626 |
rs114003789 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846618 | TTGGTTAGAAAAAAA[A/T]ATATATATGAATAAA | 57626 |
rs114007257 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823526 | GAAATTGGACTAGAT[A/G]TATATACACACACAT | 57626 |
rs114027471 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018530 | AGAGAGACACGTTTC[C/T]AGTGATTTTGAAGTT | 57626 |
rs114041578 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759785 | CAGAGCTGAGACTTC[A/G]TGCCTAAATATTGTA | 57626 |
rs114045121 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096821 | GCTGGCTACCTCCTA[C/T]TGCAGGGAAAGCATA | 57626 |
rs114056299 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043921 | ACTCATCATCTCTCA[A/G]TCACACTTCTGCAAT | 57626 |
rs114086563 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760082 | GTAAATGTCAAAAAC[A/G]TAAATTTTGAATACC | 57626 |
rs114097693 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028742 | AGCAGTTTGAGAGGC[C/T]GAAGCAGGTGAATTG | 57626 |
rs114105065 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781369 | TAAGATTGGCAGAAC[C/T]CACAATGCATGAAAA | 57626 |
rs114107518 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917698 | CATAAACCACTTTGA[C/T]AATAATTAAATGCAT | 57626 |
rs114117110 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817904 | AAAGACCTACAGAAT[G/T]TACAATGATGAGGTT | 57626 |
rs114119018 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775750 | GACTGGAGTGCAGTG[G/T]TGCCATCTTAGCTCA | 57626 |
rs114122507 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763159 | CGGTTGCACAACAGA[C/G]TTCATTAAATTTTCT | 57626 |
rs114125687 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778780 | ATAATATTGAAGGCA[A/G]GTATTCCCTCTCTTT | 57626 |
rs114132562 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802044 | CTGACAGGCCCTGGT[A/G]TCTGATGTTCCCCTC | 57626 |
rs114145047 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865352 | GTGCTAAACTAGAAT[C/T]TTCAAAAGGCTATAT | 57626 |
rs114146952 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852972 | CAAAGATAATTTATT[G/T]GTTCCTAACTTAAAG | 57626 |
rs114159678 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930223 | ATAATCCTCAGAGCA[G/T]TTTATGATGTAAAAA | 57626 |
rs114160814 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871776 | TGACCTTTGCTCCAG[A/T]TCCCAATAAGTTCCT | 57626 |
rs114163950 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822056 | TTAAAAATATTAGCT[A/G]GGTGTAGTGGCGGGT | 57626 |
rs114168273 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038504 | TCCAGAGTGGTTGTG[C/T]TATTTTACATGTCCA | 57626 |
rs114170293 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779558 | TCTTTTTCTGGGATT[A/G]CTAATGGTGTCTATA | 57626 |
rs114170510 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103710 | GATATTGACCAATGT[A/G]ACCCTGGAATTCTGG | 57626 |
rs114172481 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808472 | AGAGGCCTGGCACTC[C/T]GAAAGCACCCAGAAA | 57626 |
rs114181697 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000591 | AACAAATAAGTGACA[G/T]GAAATACATTCTCTG | 57626 |
rs114186288 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833419 | aataccagtttactc[C/T]tccaagaatggctat | 57626 |
rs114189659 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051677 | GGGCACATGATAAAG[C/T]AGCTGCAGGAACATT | 57626 |
rs114192966 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770640 | CACTGTCCTAAGACA[C/T]TAATCTTTCTATTGT | 57626 |
rs114199532 | snp | A/G | 0.127254 | 0.217792 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790712 | CACATGCATATTTCA[A/G]TAGATACAGGAAAAT | 57626 |
rs114200637 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728678 | CAAAGTGTGGTGACG[C/T]ATGCCTGTAATCCCA | 57626 |
rs114201617 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075260 | AAAGGGGAAGGCAAG[A/G]GGTAGAACTGCACAA | 57626 |
rs114204076 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094204 | ATGTGGCAGCATGCA[C/T]CTGTAGTCGCAGCTA | 57626 |
rs114204120 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742841 | TTCTTTCATTAGGTA[A/G]CTTGACATAGGAAAT | 57626 |
rs114208861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926495 | CATAGATCAGTAAAC[C/T]TAACATTTTTAAGAT | 57626 |
rs114217902 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909156 | AAATAAGTGGATGCT[C/T]AAGACAGAAAGAGAG | 57626 |
rs114229181 | snp | A/G/T | 0.0229119 | 0.104673 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949449 | GTCTCATCCCATGCT[A/G/T]TTTAAGAAACATTAT | 57626 |
rs114234194 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883832 | GGATGATACATGTTT[A/G]GAGAAGACAGAGATT | 57626 |
rs114237227 | snp | A/C | 0.0905309 | 0.192535 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828444 | GGTTCTTGGGGAGGG[A/C]AGCCAGTGGAATTGG | 57626 |
rs114237764 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829370 | CCAGCTCTCAGGAAG[C/T]TCCATCCAAAGGGGA | 57626 |
rs114240144 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079444 | ACTCACTAAATCTAT[C/T]CATGATGCCTATTTC | 57626 |
rs114262339 | snp | A/T | 0.0898077 | 0.191933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830882 | TCAAGATAGAAATTT[A/T]AAAAATTATATAAAC | 57626 |
rs114271516 | snp | C/G | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803262 | TTCATTTTATAAAAG[C/G]CTGATGAAATACATA | 57626 |
rs114278805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060899 | GTACCCTTCAGCTAT[A/C]AAAAAAGAACAAGAT | 57626 |
rs114292927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884889 | GATTTCTTTTTCAGA[C/T]AGCTCTGATAATAGT | 57626 |
rs114296526 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983739 | CATCACTGCACTCTA[A/G]CCTTGGTGACACAGC | 57626 |
rs114319760 | snp | C/G | 0.0498117 | 0.149749 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108053 | TGGAGATGCGCGAGG[C/G]AGGGAGGTCTGAGCG | 57626 |
rs114323825 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888789 | TAGGAAACTAACACA[C/T]ATCATTGGAGAGATC | 57626 |
rs114336151 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045731 | TAACTAAAGGACATT[C/T]CTGTAACACTTGTCT | 57626 |
rs114341693 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842377 | CATTAAAAAGTGGGC[A/G]AAGGACATGACTAGG | 57626 |
rs114369533 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765937 | AGTTATTGCTATTTT[A/G]GATTTTACTCTTAGC | 57626 |
rs114382323 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901061 | TAATTATTACCATAA[A/G]CAGAAACAAGAAACT | 57626 |
rs114393796 | snp | C/T | 0.030278 | 0.119257 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822884 | GAAAACAATGGCTAA[C/T]AAATATAGTGGGTTT | 57626 |
rs114405896 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828136 | ACATAGCAGGAAAAC[A/C]AAAGGAATTCACAGA | 57626 |
rs114405904 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932620 | GCATCAACTTGAGAC[A/C]TATGACAGCTCTTAA | 57626 |
rs114414416 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092329 | CACTCATCTCTTCTA[C/T]GCTGAATTCTACCTA | 57626 |
rs114424473 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837769 | TCTGGGAAAGAGACT[A/G]CCCCAGATGGAAGAC | 57626 |
rs114453606 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048740 | GGCAGTGATGCCAGC[A/G]ATGGAGAGCAGTTGT | 57626 |
rs114457297 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921492 | GTGATTTATAGTGCT[C/T]CAGATCCATGCAATC | 57626 |
rs114459897 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070146 | TGACAGAGTGAGACT[C/T]GTCTCGAAAAAAAAA | 57626 |
rs114462489 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919980 | TAACTCACTTGCTTG[C/T]TTGTATCATGATGTA | 57626 |
rs114468147 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085837 | CCACTGCACTCCAGC[A/G]TGGAAACAGAGCAAG | 57626 |
rs114468448 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749601 | TCATGTAACATGGCA[C/T]ATGTTAAAATCAAAT | 57626 |
rs114474459 | snp | A/G | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765366 | TTTGTATACTAATAG[A/G]TATCTTATACAAAAT | 57626 |
rs114484370 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736143 | AATCCATACCTCCAA[A/C]AAATGACTAATATCC | 57626 |
rs114499823 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990567 | CAAAGATCAAACAAG[A/G]CAAAGAAGGGCATTA | 57626 |
rs114501932 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892500 | GTTTCAGAAAAGTGG[C/T]TGGAAGAATCTACTT | 57626 |
rs114505819 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758974 | TCCCTAATGTTCCCC[A/C]CAGGGTGTTCTGGGT | 57626 |
rs114509718 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795962 | ATGTGAGAGAAACTA[C/T]CTTAAGTTTCACTCA | 57626 |
rs114511385 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875278 | TATTATGTTGGAAAG[A/G]CAAAAGAGAGCTGGA | 57626 |
rs114526392 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854180 | AATACCTGAGACTGG[A/G]AAATTATAAAGAAAA | 57626 |
rs114533308 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824955 | GATAATATGTATCCA[A/G]ATGTGTTTAGGATCA | 57626 |
rs114537270 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980066 | ATTTCCTATCATTGA[C/T]GGCTGAGAACTGACC | 57626 |
rs114550239 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826221 | ACACAAAATTTTAGT[C/T]AGGAAAAAGGAATAA | 57626 |
rs114552169 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808884 | AAACAGATTTTCTGC[A/T]ATTAAAAAGTTTACT | 57626 |
rs114563732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951440 | CATGTTTCTGTAGAA[C/T]CAGGTTATACTGAAG | 57626 |
rs114573088 | snp | A/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006542 | TGAGAAGGATTTGTA[A/T]TAGTTATTTGTTAAA | 57626 |
rs114594269 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062677 | TAAATATCGTACCTG[A/T]CCATGCCTATATAAT | 57626 |
rs114598530 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096886 | AAAAAGGAAGAAATC[A/G]CCAACAGAAGGCTCC | 57626 |
rs114601749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093626 | AATTGTGTATAAGGG[A/G]GGATATTACTTAATT | 57626 |
rs114602629 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759272 | GTAAGATGTGTGCAA[A/G]GCTCTGGGGGTGCCC | 57626 |
rs114606595 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028489 | AAAAGAGACCCACGG[C/T]AATTCAAAATGTGAC | 57626 |
rs114614300 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868683 | GCTTATATTTCAACA[C/T]GTGTTAAATGTTAGG | 57626 |
rs114622758 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821914 | GCACTAAAAACAGTG[A/T]CTAGGCCAGGCCCAG | 57626 |
rs114625311 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831524 | ATATCAGATATTCAA[A/G]GAAGAATTGGTACCA | 57626 |
rs114628743 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793668 | CTCTGCATACCACAC[A/G]TAGATACAAATTAAT | 57626 |
rs114634184 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840810 | TTTTATTCACCAAAG[A/G]GACTATTTCTAACAA | 57626 |
rs114636133 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730555 | AGAATTATAAAAATT[C/T]ACATCCAAGAGAACA | 57626 |
rs114649232 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886424 | GACTTAATGTGAACA[G/T]ATTTTCTAATATTCA | 57626 |
rs114652064 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829100 | TGCTCTCTTGAAAGT[G/T]CCACCTCCTGGCTGG | 57626 |
rs114693050 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882868 | TGTAGACATATATAT[A/G]AGGATCAGAAAATGG | 57626 |
rs114694276 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865544 | AAGAGGGACGGCATC[G/T]TGAAGCATGAATACA | 57626 |
rs114702612 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822245 | AAATTAGTAGCCACT[C/T]AATGAATATTGGCAG | 57626 |
rs114741954 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791177 | AACTGTATTTCTATA[C/T]GCTAGCAATAAAAAA | 57626 |
rs114742107 | snp | A/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823833 | TTCTCTCTCTCTCTC[A/T]TATGGTTGGATTCCT | 57626 |
rs114743560 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728865 | ATGAATCCATTTTCC[C/T]ATAGTAAATCATGAA | 57626 |
rs114756564 | snp | A/G | 1.66048e-05 | 0.00288134 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69707778 | CACCATGGTCCAAGT[A/G]TCTGTTTTGGGATCA | 57626 |
rs114763796 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795872 | TCTTTCTCTAAACGT[C/T]TATTGTCCTCTTCCC | 57626 |
rs114779809 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803055 | AAACAGAAGTATTCA[C/T]ATAACCAAGAGAATT | 57626 |
rs114782718 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819554 | CTGAACAGACACCTG[C/T]CTGTTAATCAAAATC | 57626 |
rs114790240 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939641 | TGTATTGCCTGTTAA[A/G]TGTGCATAAAGCCAT | 57626 |
rs114792754 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995562 | GCTGTAAAATTGCTG[A/C]AAATCTATAATGGAA | 57626 |
rs114797136 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831972 | TAAAAGCCATCTATG[A/G]CAGACCCACAGTCAA | 57626 |
rs114808004 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952584 | TAATATGCAGAGATG[A/G]AAACTCAAGTTCACA | 57626 |
rs114808510 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060672 | AACGTGGTGAAACCC[A/C]CGTCTTGACCACAGA | 57626 |
rs114809734 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766762 | TATTTTTGGGTTGTC[A/C]TAGTGCATCAGGTAA | 57626 |
rs114815452 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757092 | TAGAATTCTGAGAAA[C/T]TTTACCCAGTCCAAG | 57626 |
rs114821747 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753222 | CTCAGTGAACCCAAA[A/C]CTTCATAGCTGTTAA | 57626 |
rs114828558 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015197 | CACTTGTGAACATCA[C/T]AGAGTGGACTTATGC | 57626 |
rs114837810 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875382 | AAATAGACTAAAAAT[C/T]GATACAATTGATAAT | 57626 |
rs114843066 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929351 | TCAAACGCCTTCAGT[A/G]ATTGGGAAGATAATA | 57626 |
rs114850477 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051792 | TTATGGATTGTTTAC[C/T]AATTTGTTCTGCTAA | 57626 |
rs114851844 | snp | C/G | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806775 | AGGCATTTGAGCCTG[C/G]AGTAACCTCAGTGGG | 57626 |
rs114857704 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831010 | GTCTAAAGAGCACAA[A/G]CAGACAATCAAAGAT | 57626 |
rs114865062 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795445 | TGTATGTTCTAAATA[C/T]AGGAAAGGAAGCACT | 57626 |
rs114865322 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771351 | CATCTATTATATTTA[A/C]AGTTGGCTTAAGCAA | 57626 |
rs114866128 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757288 | ATTGTTAAAGATGCA[A/T]TTAACAAGACAATTT | 57626 |
rs114881736 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014386 | TCAATACATTTATGT[A/G]GCTATACAATTCACT | 57626 |
rs114909406 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929688 | GATCAATATTTAATG[C/T]TAAGAATATATTATG | 57626 |
rs114920434 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990202 | TGGAAAGACCATTAC[A/C]AGCCACTATGAAACA | 57626 |
rs114920898 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828940 | CAGATATGCCTAACC[C/T]TGCACCCACCAAGCC | 57626 |
rs114931039 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943132 | CCGTATAGGTGATCT[C/T]GTACCCTGCTCCATC | 57626 |
rs114947237 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901490 | TATGCTTGGGTGACA[A/G]TGATGACTCTGGTCA | 57626 |
rs114975446 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802312 | TGCTATTGTAAATGG[C/T]GCTGCAATAAACATA | 57626 |
rs114979784 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828467 | GGAATTGGGAAAGGA[A/C]CACAGGGAGAAGGAA | 57626 |
rs114983893 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876403 | TTCTTGCATTGCTAT[G/T]ACCACTACAAGTAAT | 57626 |
rs114984544 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722667 | TAAATGCTGATGAGG[A/G]TGTGAAAAAGGAGAA | 57626 |
rs114985326 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870911 | GCCGCTCTCAGGGAT[C/T]GAAACTGACTGCTTG | 57626 |
rs114989437 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801033 | CGAATTACTCTGTGC[A/G]TAGAATATACATTAT | 57626 |
rs114990628 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948385 | AAAAATTGTGTCACA[C/T]AATCATGCCTAACTC | 57626 |
rs115019727 | snp | C/T | 0.030278 | 0.119257 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922042 | CAAGGCATTCTCTTG[C/T]CTCAGAATCCTGAGT | 57626 |
rs115024507 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873635 | AGACAAATAACATAT[A/C]AACAGATAGGAGAAA | 57626 |
rs115037072 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020983 | ATTATCAACATCCCC[C/T]ACCAGAGTGATACAT | 57626 |
rs115046942 | snp | C/G | 0.039522 | 0.134904 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019558 | TCCATGCCAGACGAT[C/G]TGCTAAATTATTTGC | 57626 |
rs115062383 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823468 | AAAATCATTAAAATT[A/G]TTTATTTTAAAAATT | 57626 |
rs115071346 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779164 | ATTAAAAAATCTTCA[A/G]TAAATGTTTATTTGA | 57626 |
rs115074845 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941300 | ATTCCAAAAGGAAAC[A/C]TCAAAACTATACAAA | 57626 |
rs115077634 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018456 | GTAATAAGGACCTCA[A/T]CTAAACAGATGGACA | 57626 |
rs115084649 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808936 | TGGAAGCCTTAACAG[C/T]AGACTAGACCAAGCA | 57626 |
rs115087297 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992913 | TTTGTATATAAATAT[G/T]CTGCAGAGGGAAAAA | 57626 |
rs115091984 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899666 | ACATACACGGCTTTC[C/T]AGGCACTGGCAAATA | 57626 |
rs115097131 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878620 | TAATTATATGTTACA[C/G]TATATGTAACATTAC | 57626 |
rs115098763 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799254 | GAACAACTGTACTTC[C/T]CACAGACTCCAAAGC | 57626 |
rs115103280 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900509 | CAGTAATCCACTTAC[A/G]AATATGTGCTTTGTT | 57626 |
rs115103943 | snp | A/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826247 | AATAAGTTAGAGATC[A/T]ATTATATAATAGATC | 57626 |
rs115105517 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820764 | GCAGGTAGAACAGGA[A/G]GTTGCCCGTGCTGTG | 57626 |
rs115109941 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781326 | ATATCAAGTTCATGA[A/G]AAGGAATTTTGAGGT | 57626 |
rs115112120 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708048 | AAAATAATGTCATGA[A/T]GTCTTTCTACAAAAA | 57626 |
rs115117296 | snp | A/C/T | 0.368938 | 0.219895 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757793 | AAATCTCGTCCCTAC[A/C/T]AAAAATGCAAAAAAT | 57626 |
rs115130046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019532 | AGTACCATTTAACAC[G/T]TATTACATACTCCAT | 57626 |
rs115134156 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917551 | GGAATGGTTGATTTC[G/T]TTTCTGTGGCAAGGA | 57626 |
rs115155149 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044767 | CATTTTAGGATTAAA[G/T]TAAGACTAGACAATT | 57626 |
rs115180315 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093117 | TGAAAATAAGCTATA[A/T]GATGCGCTATTATGT | 57626 |
rs115191088 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778549 | ACATAGTTCTTGATT[A/G]TACAAGAGATATCTA | 57626 |
rs115201450 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900559 | TGTTGAGCAAGAGAC[A/G]CCGGGTTTTAGTGGA | 57626 |
rs115211104 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958066 | TAAATAGTTGCAAGA[A/T]TTATTATTTTTTTAA | 57626 |
rs115212086 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928263 | CTCCTTGTTCCATAA[C/G]TTCACCTTGCAGTTT | 57626 |
rs115213269 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831337 | TACATGCACAAGCTA[A/G]AAAAGCTAGCAGATT | 57626 |
rs115218829 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833470 | TAGATGTCGACAAGG[A/T]TGTGGTGAAAAAGGG | 57626 |
rs115231143 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100724 | TCAGATCTTTTCTTT[A/G]AAGTTTTAAATAACT | 57626 |
rs115235176 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827764 | AAAAGTTATTCTTAG[C/T]ACATCTCATCATTAA | 57626 |
rs115238584 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838201 | CTTAATAACAATTTT[A/T]AAAAAGATGTTGGAT | 57626 |
rs115270299 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880680 | GCACAGGTGGCAGCA[C/T]CTCCCTATAACTGAT | 57626 |
rs115272908 | snp | G/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957474 | TATGCATTCGCTATA[G/T]TCCTTGATTTACAAC | 57626 |
rs115283146 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003411 | AAATATTTTCAATGA[C/T]ATGTTAAATACATTC | 57626 |
rs115287289 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001027 | TAAGATAGAAATAGA[A/G]GATATTAGAGACAAA | 57626 |
rs115292760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806663 | GGCCATGGGAGAAAC[A/C]CTTGACCAACCACTA | 57626 |
rs115293907 | snp | A/C/T | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928685 | TCTCACAAAACCACA[A/C/T]ATTGTATGATTCCAC | 57626 |
rs115297558 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830369 | GGACATTAAGTAATG[A/G]TAAAAGGACTTGTCC | 57626 |
rs115299584 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762364 | TCCCTAAAATTAGAT[C/T]AGCTTCTCGACTCTG | 57626 |
rs115311475 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849075 | CATCCGATTTGGGCT[A/C]AGCACTTTTCATTCC | 57626 |
rs115331037 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920144 | GATAAAATTTGTTTG[C/T]TTTTGGCTCTTTCTA | 57626 |
rs115358148 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091611 | TCATTCCCTGGCCTT[C/T]TTCTACCTTTCCTTC | 57626 |
rs115360570 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720106 | CTTACTCAGTGCCTA[C/T]ACTATAGCTAAAAAC | 57626 |
rs115363760 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739467 | AATGGCAAGCTGGAT[A/G]GAGTCAAGATTCATT | 57626 |
rs115369674 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969151 | ATAATTTAACTTAAA[A/C]ACAAAATACATTCTT | 57626 |
rs115372433 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983718 | GTCGGCAATGACCTG[C/T]ACTCACATCACTGCA | 57626 |
rs115379648 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821915 | CACTAAAAACAGTGA[C/T]TAGGCCAGGCCCAGT | 57626 |
rs115385278 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870390 | ACCCCACGACCCAAA[C/T]ACTTCCCATTAGGCC | 57626 |
rs115388743 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775716 | TTGTTTTTGATACAG[G/T]GTCGTGCTCTGTCAC | 57626 |
rs115411198 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712027 | GGATATCACCTCTTG[A/T]AGAGTTCTTGTTCAA | 57626 |
rs115426098 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753497 | TCTGTTTAAATGAAT[C/G]AATGAAGATGACAAA | 57626 |
rs115427824 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780042 | CTATCTCCTGATCTC[A/G]GGTGATCTACCCACC | 57626 |
rs115463646 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762903 | ATGGGAAATGAAGGG[C/T]CAATGTAGATAAGGA | 57626 |
rs115465139 | snp | C/T | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791862 | AAATCTTCATGAACA[C/T]AGATTAGAAAATAAT | 57626 |
rs115465479 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756237 | GTTGGATAACTCTGT[A/G]GCAGTTATTGATAAT | 57626 |
rs115469077 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795509 | AAGAAAGTAATTTGT[A/G]CTTCTCCTTACAATC | 57626 |
rs115469576 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054807 | CAGAGTCTCTTAACA[C/G]TAAAATTGATCAAGC | 57626 |
rs115471863 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092280 | TTTCTAAACTATTGT[A/G]CCACCCAAAACTACT | 57626 |
rs115475614 | snp | C/G | 0.00597247 | 0.0543191 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108239 | GCGTACCCCTCGCCA[C/G]ATCTCTTGGTGCACC | 57626 |
rs115487198 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885300 | TAATTTTGTATTTTT[A/G]TAAGTTACACTAAAT | 57626 |
rs115490782 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952075 | ATAAATGTAAGCAAG[A/G]GGGTTTGATTACAAG | 57626 |
rs115504080 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810224 | ATACTCTACCCAACA[A/G]CCACAGAATATATAT | 57626 |
rs115504679 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826539 | TAGCCAAGATCCTGC[C/T]GTTGCACTCCAGCCT | 57626 |
rs115505735 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031443 | GATGCAGAGGTTAAC[A/G]GTTACTCAAAATTTA | 57626 |
rs115510276 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895533 | TGTAACAAATCACCA[C/T]AAATTGTGTGGCTTT | 57626 |
rs115520950 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041675 | AAAATCCTGACTTTC[C/T]ACTAGTGCCACTTTG | 57626 |
rs115536153 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849280 | TTAAGAGTATACATT[A/C]GTTTGTTATTGTTTG | 57626 |
rs115548203 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723124 | ATACTCTAAAAAGAA[A/T]GTCTCATAGAATTTG | 57626 |
rs115549345 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831817 | GTCAATAGATGTGCT[A/G]CACAACATAAACAGA | 57626 |
rs115550322 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703855 | GTGTGTAGTAGGCCA[A/T]ACCATCTGGGTTGGT | 57626 |
rs115569839 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859482 | CTCCAGTAGGGCAGA[C/T]GCTGTGACAGCTCTG | 57626 |
rs115592740 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032960 | CTCTTAGTTTTTGAT[A/C]ATAGATATTTTGAAT | 57626 |
rs115593282 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998312 | TGATCTATTGATTCT[C/T]TAGCTAGCCCACTTG | 57626 |
rs115594194 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780892 | CTCATTGATTCTGTT[G/T]CCCTGACACATGAGC | 57626 |
rs115595994 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053649 | AAAAGAAGGAGACTC[A/C]ATAAATTATCTTCCA | 57626 |
rs115597291 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982759 | ATATCAGATAAAATA[G/T]ACTTTAAGACAAAAA | 57626 |
rs115627544 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721328 | ACACATATTGATTGA[C/T]GTCTCGTATCTCCCT | 57626 |
rs115632543 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745995 | AAGATTTTAACTTCC[A/G]GAGTAATGTTTGTTT | 57626 |
rs115644429 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881919 | TGCATCTTATATCAA[A/G]TAATTGACAGGAGAC | 57626 |
rs115647251 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821124 | ATTATGAATTTTTTT[C/T]CCAATCATTATAATG | 57626 |
rs115649459 | snp | A/C | 0.0626037 | 0.165477 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832558 | CAATGCAATTCCCAT[A/C]AAAATATTTTCATTC | 57626 |
rs115653785 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715938 | GTATTTGAACAATTG[C/T]TTACCTCTTGAGGCC | 57626 |
rs115653934 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827353 | ACTTGAGAACTGATT[C/T]TAATCTTCAGTAAAA | 57626 |
rs115656900 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867795 | AACAAAATAATAAAT[C/T]GAACAATGAGAACAC | 57626 |
rs115666766 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774806 | TTGAACTGACTACCT[A/G]TGTGTTATCTTTTAT | 57626 |
rs115681714 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802020 | TTTGTCCCCTTGCCC[C/T]CCTACCCCCTGACAG | 57626 |
rs115684851 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741614 | GTAATCAAAGTGACC[G/T]TACTGTTTCCCTTCT | 57626 |
rs115696519 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793303 | TTGTAGCATACTGAG[A/G]AAAGTGTGGTCTTAA | 57626 |
rs115707281 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882114 | AGGATTTAGATCCAC[A/G]ATCCATCATCATACA | 57626 |
rs115711072 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953632 | AAAATCATGAATATA[A/C]AATAAAAATCCATCT | 57626 |
rs115723544 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823976 | TGTGTATATCATTAT[G/T]TGTGTGTGTATATAT | 57626 |
rs115724464 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839869 | TGCACACATCCAAAG[C/T]ATCTTTTATTTTCCT | 57626 |
rs115753526 | snp | A/T | 0.0456336 | 0.143994 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033999 | CATTCTCTACTCAGA[A/T]ATATCCCATGACATT | 57626 |
rs115758491 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802382 | TTTGAGTATATACCC[A/C]AGAACTCCCACTATT | 57626 |
rs115763435 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811306 | TTTTATTGCTGGGAT[A/G]CAAGGATAATTTAAC | 57626 |
rs115763809 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834693 | TTAATAGTAAGTGTT[G/T]CTAAAATTAGAAAGT | 57626 |
rs115775601 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873823 | ACTTGTATTTGTTTA[C/G]TCAGTAAAAATTTGA | 57626 |
rs115788318 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858992 | TATTCATATACGTGT[C/G]CATCCAAACTTCCAT | 57626 |
rs115793376 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887096 | TATAATCTTTGGGTC[C/T]AATGTTTTGGGTCTA | 57626 |
rs115798335 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990751 | TAGACAGATCATTGA[A/G]GCAGAAGATGAACAA | 57626 |
rs115822405 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836091 | CCCAGAAAGAGGGGA[C/T]GTGAATGGAAATGAG | 57626 |
rs115824624 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780104 | TGAGCCACCGTGCCC[A/C]GCCATTTTTTCTATT | 57626 |
rs115826868 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925819 | CTCTCATTCATGAGA[C/T]AAATATGAGATAAAT | 57626 |
rs115829552 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829741 | AACCTATCAAATTAA[C/G]ATCAGATGTCTCAAC | 57626 |
rs115834098 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737997 | TTCAGGCTGGCATCA[G/T]GTTGGTGCCCCTCTG | 57626 |
rs115834476 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776693 | GCATTTGTTAAAAAA[A/G]GAAAAATATAAAATA | 57626 |
rs115835821 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769197 | ACATTAGGCCCAACT[A/G]CTAAGGTTTGAAAAA | 57626 |
rs115845712 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947707 | CTATATCCAATGAAA[G/T]AATCCATTTGTTAAA | 57626 |
rs115846958 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968415 | GACTTGCTTAATTGC[A/G]ATAGTCACTTCATTA | 57626 |
rs115848993 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998613 | TCTCCTGTTTCATCA[C/T]TTCTACCTCAATCAA | 57626 |
rs115850371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900007 | GAACTTACTATAACA[C/T]TGTTAATTCTTAATA | 57626 |
rs115855734 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849034 | ACCCTGTATGAACAT[C/T]GCCTTCATCCTTAAT | 57626 |
rs115882166 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872893 | ATGACACAAACATCT[C/T]TCATTAGGCCCCACC | 57626 |
rs115891595 | snp | G/T | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822823 | TAATTATCTGATAAA[G/T]ATTAAATTGATATTG | 57626 |
rs115897744 | snp | C/T | 0.16911 | 0.236552 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777100 | TGATAGTAAGTCACA[C/T]GAGATCTGACGGTAT | 57626 |
rs115902546 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769456 | GACAGGGATGGGTCC[C/T]TGGTGAAACCCAACC | 57626 |
rs115903216 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797246 | GGTGAGCATGACCCA[A/G]TTCTGTCAGTGGATT | 57626 |
rs115906857 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761776 | TCATGGGGAGTCTCA[A/G]TGGCTGCCTGGTTTT | 57626 |
rs115924884 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889389 | AAGCTAAGAGGAGCT[C/T]GCATATAGTCATACT | 57626 |
rs115928344 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788995 | ATTCAGGAGAAAAAG[A/G]TAAACACTGGACTCC | 57626 |
rs115932038 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779921 | GTTCAAGTGATTCTC[C/T]GGCCACAGCCTCCGA | 57626 |
rs115943222 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730654 | ATCACAGCTCACTAG[A/C]CTCAACTTCCTGATT | 57626 |
rs115946208 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722739 | TACGAAAAACCATTA[C/T]GAAAAACAGTTTTTT | 57626 |
rs115968282 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823011 | TAAGACGTCAAAAGT[A/T]CGCTATCAAGAGCTT | 57626 |
rs115975969 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063188 | GATTACTTCTCTAAG[G/T]AGACTATGCTAGGTG | 57626 |
rs115977300 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806698 | CTCATGTCTGATACA[C/T]GGAGCTGCCTAAAGA | 57626 |
rs115977311 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757124 | GATATGATCCTAAAT[A/C]TTTTAGAAACCTACA | 57626 |
rs115998419 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778455 | AAGAAATCATTTCTA[C/T]TCAGTCCACAAATTC | 57626 |
rs115999201 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924484 | ACCCCTTCTGAGAGC[C/T]GAACACTCATTGGGA | 57626 |
rs116009206 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101832 | AGAACACCATGTAAC[A/G]TTTATAAATTCATCC | 57626 |
rs116025818 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921187 | TTGGCAAAAAGAAAC[A/G]TTATAAACATCTTAC | 57626 |
rs116031349 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881166 | ATTTTGCTGTTTTTT[C/T]CTCCTGTACTAATCT | 57626 |
rs116032241 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831749 | AAAAAGATAGTCCAC[G/T]ATGATCAAGTTGATT | 57626 |
rs116032745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946027 | GATTATGAAATACCA[C/T]GGTTACTTATGTTGA | 57626 |
rs116035298 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851723 | CCCTGTTCTCTATTA[C/T]AGACCTTTCCTGTCC | 57626 |
rs116044770 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063592 | CGATATCAGAAACTT[C/G]AATATAAGTAAAATA | 57626 |
rs116047177 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098014 | CTATTTACTAGCTAA[C/T]TAAACTTGAAAATAT | 57626 |
rs116053544 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972430 | TAGGATACTTTTCTA[G/T]CTATCAAATATCATC | 57626 |
rs116069300 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831944 | GGCATAGAGGGGACA[C/T]ACTTTAAGATAATAA | 57626 |
rs116072983 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766228 | CACCATATGGAAAAC[A/G]GCAATCAAATATAGG | 57626 |
rs116074247 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798618 | ATGTATTTTATATTT[C/T]AATATATTTATTATA | 57626 |
rs116075255 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770711 | AAATATCTCTGCTCT[A/G]CAATAGAATAATAAA | 57626 |
rs116091140 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019740 | CCTTTATCCATATAT[G/T]ATACTGTCTCTTGAA | 57626 |
rs116099025 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938464 | TTTGTTACTATTGTG[C/T]GATAAATTGCAGAAT | 57626 |
rs116101265 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903082 | ATAGATGGATTCTCA[A/G]TGGACTCCCTGTGGC | 57626 |
rs116102555 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852420 | AGAGACAACATTCAG[C/T]TGATTAATTGGAAAA | 57626 |
rs116107236 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762722 | TTCCCAAGATCATAA[A/G]TTAAGATTTCTCTGC | 57626 |
rs116118109 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705250 | ACAAAAAATAAGCTC[A/G]GTGTTCAATGACAAA | 57626 |
rs116145493 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872792 | GCAAGGCTCTTTTTA[A/T]CAACCGGCTCTTGTG | 57626 |
rs116146620 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850511 | TACTCCCAAATACTG[C/T]TGATTACTATGAAAC | 57626 |
rs116148422 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946688 | CAGCTATTTATTTTT[A/G]TTTTTGTAGCAATTA | 57626 |
rs116150031 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922841 | AAAGGTCTATTCCTT[A/T]AGTTGGGTAGTACTT | 57626 |
rs116153009 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768337 | TATCTGAAATTATTA[C/T]ATTACACAAAGCTTC | 57626 |
rs116164594 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823994 | TGTGTGTATATATAT[A/G]TATATGTGCATATAT | 57626 |
rs116170375 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989139 | AATGATTTTTGTATA[C/T]AGTGTAAGGAAGGGG | 57626 |
rs116172767 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988787 | GTCTTCATGTCTTTG[C/T]CCACTTTTTAATGGT | 57626 |
rs116175401 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015748 | GGTTAGGTGTATTAA[A/G]TGAATTTTCAACTTA | 57626 |
rs116178158 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903372 | CAAACCCACCAGAGC[A/G]CATCTGCCCCAGCCA | 57626 |
rs116188708 | snp | A/C/T | 0.368938 | 0.219895 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757791 | TGAAATCTCGTCCCT[A/C/T]CTAAAAATGCAAAAA | 57626 |
rs116189717 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077453 | CGTTGAAGAGTTTGG[C/T]GGGAATAATGAATAT | 57626 |
rs116200472 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931014 | CATGGTATGTACTAT[C/T]ACCACCTTAATTTGT | 57626 |
rs116214180 | snp | G/T | 0.105569 | 0.204058 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982790 | GGAAGAAAATACAAA[G/T]AGGGTCATTATATGA | 57626 |
rs116222118 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776743 | CTTACAAAAACAAAA[A/G]CATGCAATAAATTAG | 57626 |
rs116226159 | snp | G/T | 0.0554779 | 0.157039 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097586 | TCTTGGACCTCTTTA[G/T]GTAGAATCTATACTT | 57626 |
rs116230064 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874839 | GAGAAGTAGCTTTGG[A/G]GTAAATGATGTAGGG | 57626 |
rs116231963 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929147 | AAGCTGCAAAGAACC[A/C]CAAAGGACCATTTTG | 57626 |
rs116253005 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826125 | GCTAAAAAAGTCAAA[C/T]TCATAGAAGCAGAGA | 57626 |
rs116256078 | snp | A/T | 0.0168055 | 0.0901129 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798730 | CTGGATTCTCAAAGC[A/T]TGATAACTTTTATAT | 57626 |
rs116259772 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739402 | AATTCACACATAACC[A/T]TATTAACCTTGAATG | 57626 |
rs116264217 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966180 | TAAAGAAGATGTCAT[C/T]TAGGATTTTCATAGT | 57626 |
rs116268536 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866316 | ATCTGGTTTTCCAGC[A/T]CAGCAAAGCCAATTT | 57626 |
rs116281201 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039678 | AGAGTTTTACTTTGT[C/T]GCCCAGGCTAGAGAA | 57626 |
rs116289291 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887292 | AATTTTCAGTCTTCT[A/G]TTTCATCGGATATAA | 57626 |
rs116291747 | snp | G/T | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835541 | GAATGGTTAAAGGGG[G/T]CTGACATGGCTCTAA | 57626 |
rs116324760 | snp | G/T | 0.0898077 | 0.191933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831787 | AGGGATGCATGGATG[G/T]TTTCAAATATGCAAG | 57626 |
rs116341455 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774770 | TTAACTTTGCAGAAT[C/T]TGTTGCTTCTGAGGA | 57626 |
rs116352978 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904257 | TACCTTGTTTAAATT[G/T]TATGAGTCTCAACCA | 57626 |
rs116372336 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018219 | TTAATACAATCGTTA[C/T]TCACAAGTACCCTAT | 57626 |
rs116383398 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713462 | TTTATTTTTCAAGTT[A/T]GGTGAGCATTTTTTA | 57626 |
rs116411500 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782181 | ATATAGTATTGGCTG[A/G]GGAGTCAAGATGGCC | 57626 |
rs116419352 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928211 | GTTTGAAGACTCTCA[C/T]AGAGGAAAATCATCA | 57626 |
rs116421254 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000442 | AAACAAGAAAAAAAG[C/T]GTATATACATTAGTT | 57626 |
rs116436953 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061263 | GGAATTTGTCTTAGA[A/G]TGTAGCTACACAGGA | 57626 |
rs116438559 | snp | A/G | 0.039522 | 0.134904 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096454 | GATTAATGATGGTGA[A/G]CATTTTTACATATAC | 57626 |
rs116446485 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827222 | ATGAAATGGAAATAT[A/T]ATAGAGCATATTTAA | 57626 |
rs116447616 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829414 | CACATCAAGGAATCA[C/T]TGTGCAGGACAAAAT | 57626 |
rs116448477 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847571 | TTAAACATATTATAG[A/G]CCAAAGAAAAAGTAC | 57626 |
rs116458840 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918860 | CCTCTCCATCATCTT[C/T]ATAAAACACGGGTTG | 57626 |
rs116467383 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764279 | CCAATCAAGTTGTTT[A/C]CATACACTGTTTTCT | 57626 |
rs116469627 | snp | A/T | 0.116488 | 0.211364 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711163 | GAAAATTGTTTTAAA[A/T]ATAAAAACATTACTT | 57626 |
rs116516303 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809881 | ATGCAAATGGAAAAA[A/T]AAAAAGCAGGATCAC | 57626 |
rs116536273 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774196 | GAAAAATTAATCATA[A/G]TGAACTATTTTTTGT | 57626 |
rs116556869 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025140 | CCACTATTTGAAGCT[A/G]CCACTCATTTAAATT | 57626 |
rs116558813 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052743 | TTCTCTCTCTCTCAC[A/G]TGCACATACATAGGC | 57626 |
rs116564014 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987850 | AAAAGTTTCAGAATA[A/T]TGGAACTAAAATAAC | 57626 |
rs116569580 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825949 | GAACTTTTATTTGAC[A/G]TTTATACAACATATT | 57626 |
rs116571332 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844975 | GGAAATATTTGCTCC[C/T]GCAGGATGAGACATC | 57626 |
rs116574980 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988011 | GGCTTGTTATAGAGG[C/T]GAACTCATGACTCGA | 57626 |
rs116585172 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757108 | TTTACCCAGTCCAAG[C/T]GATATGATCCTAAAT | 57626 |
rs116585286 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078566 | ACACAAACAGTTTTC[C/T]AGAATTTGAAAAGCC | 57626 |
rs116613773 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957623 | TTGTTAGCAGAATTA[C/T]GATTTGATTTTGAAA | 57626 |
rs116625028 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720194 | TTTACTTGATACACT[C/T]ATCTTGCTATAATTA | 57626 |
rs116649468 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022701 | GGGCTACACGGTGAG[A/G]TTGGATGAATTTAGC | 57626 |
rs116649802 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000058 | GGGTCTGTTAGTTCC[C/T]ATGAGATCTGATTGT | 57626 |
rs116655621 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772263 | ATTATAATAATGTAC[A/C]TATTTTATTTATAAA | 57626 |
rs116659119 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849076 | ATCCGATTTGGGCTC[A/G]GCACTTTTCATTCCT | 57626 |
rs116665109 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917964 | TCTGTATTCATACAT[A/G]TACTCCACAGCACTG | 57626 |
rs116673002 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828246 | AAGTCAGCCTCCAAG[C/T]ACATATGCTCACCTC | 57626 |
rs116680143 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971124 | GTTCTAATGTCACCA[A/G]TTATTGAGTGAATAA | 57626 |
rs116690190 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822266 | ATATTGGCAGCAGAT[G/T]TAGATAATCCCAAAA | 57626 |
rs116698630 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937986 | AATTCTATCCCACGT[G/T]TAGTAGAAAAAATGG | 57626 |
rs116706805 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887684 | TCAATTACCAAAAAC[C/T]CATTCCTCATTTCAG | 57626 |
rs116709909 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728919 | TGCAGATTCTTAAGG[G/T]GGTGGTACTACATAT | 57626 |
rs116712092 | snp | A/C | 0.0221141 | 0.102801 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700265 | CAAATATTTTTGGCT[A/C]CCTAACAATAAAAGT | 57626 |
rs116732774 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024571 | ATTCAGGAGGTTATT[C/T]CCCCAATGCCCCATT | 57626 |
rs116734363 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090647 | TTTATGCAAGGCACA[A/G]AAAGAAGATCTGAAA | 57626 |
rs116736437 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927757 | AACAACAAAAATTAT[C/T]GGCAAGTATGTAGTT | 57626 |
rs116743032 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989344 | ACTAGTATCATGTTG[C/T]TTTGCTTACTGTAGC | 57626 |
rs116749391 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716206 | TCAATTCATTTGTCT[C/G]TATAACAACCTATTT | 57626 |
rs116752393 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866583 | AAGCCAGGGATTCCG[C/T]GAGTTAGAGTTAAGT | 57626 |
rs116754867 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828812 | CTGGCAACCTGTATG[A/G]CGCAGCAGAAGCAGC | 57626 |
rs116772021 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967416 | ACCTCTAACCAAAGA[A/G]TTAGAATTAGAAGTG | 57626 |
rs116774682 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791966 | TGCTTCCAAAGGCAC[A/G]ATTAAGAAAATTGCA | 57626 |
rs116776093 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795738 | AATAGAAAGTGATAA[A/G]TTCAAGATGCACATC | 57626 |
rs116788337 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939492 | TACAATATGCTGTGA[C/T]GGAGAGGTTTAAAAA | 57626 |
rs116805311 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995561 | TGCTGTAAAATTGCT[A/G]CAAATCTATAATGGA | 57626 |
rs116806791 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036009 | AAATGCTTCAATGAT[A/G]AGTATCAACACACTG | 57626 |
rs116813524 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729353 | TAAACCAATTTCTTG[G/T]TTTTTTCTTCCACAA | 57626 |
rs116826845 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834982 | AAGGTGGGATTATTT[G/T]CATTTTAGAGATGTA | 57626 |
rs116828831 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885485 | TGCTGTTTTATTTTT[C/T]CATCAAGCCTCATTT | 57626 |
rs116830796 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744068 | AAAAGTGTTGGAGTT[A/G]TCAGCAATTATATGG | 57626 |
rs116860298 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023560 | TTTTTTAATCTAGGA[A/G]CCAGCAAGTTCACAA | 57626 |
rs116867542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739334 | TGACACTATGAAGCT[A/G]CTACATAGACAAGTC | 57626 |
rs116878107 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856284 | GTTCTCTAAGCTCAA[C/G]TTTCCTTTTTTGTAA | 57626 |
rs116878539 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925381 | AGAACACAGTCTGGC[A/G]TATAATAATCCACTA | 57626 |
rs116878791 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813885 | TGTTTTTCACAGACT[G/T]AGAAGAACTTTTCTA | 57626 |
rs116918578 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898759 | GTGCCATTGCCTCTT[C/T]TGACAAATTAAAAAT | 57626 |
rs116943539 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859545 | CCGCATTTTCACCAT[A/T]GTTCGAGTTCTCTGA | 57626 |
rs116945011 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720810 | GGGCAGAGGCTGAGG[G/T]GAGAGTGGTGGTTCA | 57626 |
rs116951090 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002509 | TGTAGTCCCAGGAGG[A/C]AAGGTGAGAGGGAAG | 57626 |
rs116969340 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048443 | CATCATTCAATATCT[A/G]TAGGTAGATACAACA | 57626 |
rs116983815 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927854 | AGAATGTTAAACATG[C/G]AGTTATTGTATAACC | 57626 |
rs116986029 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024803 | GGGGTACTCAAGAAA[C/G]TTGAGGAGCTGCAAT | 57626 |
rs116990649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763567 | GTGTGATCACGAGGA[C/T]ACTTTAACCTATGAA | 57626 |
rs116992818 | snp | A/C/T | 0.0071688 | 0.0595163 | intron-variant | KLHL1 | GRCh38.p7 | 13:70049763 | CCAAGATAAACAATG[A/C/T]GGTGTTTCGAGAACA | 57626 |
rs117003969 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980706 | AAAAATAGATTCAGG[A/G]GATAGATGTGCATTT | 57626 |
rs117007198 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771766 | TTAAAAATAATTTTG[A/T]GTGAATTCTATTTAA | 57626 |
rs117031154 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853386 | AGGATGTTGTTGCTT[C/T]TCCTTCCACCATGAT | 57626 |
rs117057351 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035293 | CAACAACATGGATGG[A/T]ACTGGAGATCATGAT | 57626 |
rs117109797 | snp | A/T | 0.0165278 | 0.0893908 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958905 | TACAGTTACCTCCTA[A/T]GCTTCCCTTTCTATA | 57626 |
rs117109948 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763933 | CCTGAAGTAACCATT[A/T]TTTTTTCTATTGTTC | 57626 |
rs117110832 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062081 | GTATTCCTTAACCAG[A/C]CTCTCCCCATCTTCC | 57626 |
rs117117812 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829878 | GAAGAAAAGATATAA[C/T]AATATTTAGACAAAG | 57626 |
rs117123158 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888981 | GATAGCAAATATCAA[C/G]AGTTATAAATAAAAT | 57626 |
rs117128197 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103716 | GACCAATGTGACCCT[A/G]GAATTCTGGCTTGCA | 57626 |
rs117129483 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904701 | TACAACTTTACACAG[C/T]GTATGAATGAGAAGG | 57626 |
rs117133386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703650 | TGCAAGCTTCATTCA[C/G]GTTAAATAAAAGAGG | 57626 |
rs117148460 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976838 | CAATCAGGACTTAGA[A/C]AGCTAAGATCCTGAA | 57626 |
rs117150825 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019839 | ACTTTATCTCAAATG[C/T]GACAGTGTTAAGATA | 57626 |
rs117162584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089281 | TTCACTGTTGTTGCC[A/G]TCAGTTGTTTTGTTT | 57626 |
rs117190638 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103742 | TTGCACAAACTAATT[A/C/T]GTAGAAAGCTATTCT | 57626 |
rs117222953 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952401 | TACCAGTCTTTAGAA[C/T]TTCTTTATTAACTTT | 57626 |
rs117228023 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935246 | CACCCACTGGTGAAC[G/T]TGGTACATAGTTCAC | 57626 |
rs117242842 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917121 | AGATTTGTGGGGAGC[A/G]CTTGAAGAAAAAATA | 57626 |
rs117251871 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701418 | TCAAGAAAAAACAAG[C/G]CTTTGGTAACTCTAG | 57626 |
rs117256294 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718215 | ATCAGCTAAACATCT[C/T]GCTTTTCTCCCAGAT | 57626 |
rs117264389 | snp | G/T | 0.191775 | 0.243125 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837701 | ATACACATATATATA[G/T]AGATCTCATATTTTT | 57626 |
rs117264430 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095803 | TAACTGTATTTTTGT[A/G]TTGAATAACTGTCCC | 57626 |
rs117272803 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870784 | GACATTAAATCTTGA[C/G]ACTCCAAAATCATCT | 57626 |
rs117274856 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758505 | CTTACACAAAAATCA[C/T]ATCTTCATGCCTTTT | 57626 |
rs117278584 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013645 | ATGTTTCCTTAGAAT[A/T]GCTTAATAAAAATTC | 57626 |
rs117306163 | snp | A/C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789613 | AGTAGAATGAACAAA[A/C/T]GACCATTTTTTTTCC | 57626 |
rs117307682 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072446 | CTGTGAAGTCATGAG[G/T]TCAGTATCCCAGTAA | 57626 |
rs117309228 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823476 | TAAAATTATTTATTT[C/T]AAAAATTATTTACAT | 57626 |
rs117319917 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701050 | AGTTTCAGATTGCCA[A/G]TATGGTTGCAATAAA | 57626 |
rs117326976 | snp | G/T | 0.444133 | 0.157519 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978545 | AGGTTGGGGTGCAGT[G/T]GCACGATCTTGGCTC | 57626 |
rs117351956 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832606 | AAATTCTAAACCTCA[C/T]GTGGAATCAAAAAAG | 57626 |
rs117362860 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992671 | TCTTTCCTTATTTTA[C/T]TTCATTATTCCAAAA | 57626 |
rs117366011 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962412 | TGCAAGTTATATTCT[C/T]TTGACTTATTCCTGT | 57626 |
rs117409997 | snp | A/T | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918307 | ATTGCCATATTTTAA[A/T]TAGTTGATTTATCTT | 57626 |
rs117437227 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957949 | TTCTGTGCTGTTACA[A/G]TGTGGGAAAAACTGA | 57626 |
rs117438683 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924502 | ACACTCATTGGGACA[C/G]CCTAGCTGCAGAGTG | 57626 |
rs117450285 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896514 | TTTTCATGCTTGTTA[C/T]TAAAAAAATAGTGCA | 57626 |
rs117486559 | snp | C/G | 0.0165278 | 0.0893908 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022018 | ATCAATTTTTTCAGA[C/G]ATCATTCCTTTGGTG | 57626 |
rs117487473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988509 | TGGGTTGAATGTTAG[C/T]TCAGTTTTTAGTTGA | 57626 |
rs117500037 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929246 | CCCAGTTGTATTAAA[C/T]ATTGTTAAAACGTCA | 57626 |
rs117516608 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017069 | TGAGAACTGTTCTGC[C/T]GCTCAATGAAGCTCT | 57626 |
rs117527163 | snp | C/T | 0.04875 | 0.148319 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040999 | TGTTCAGAAATTCTT[C/T]GTTTGACATCTCCAC | 57626 |
rs117542059 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864623 | AAAAAATTCCATACT[C/T]ACAAGGTAAAGACTA | 57626 |
rs117544024 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932066 | AAATTATTAATATGC[A/G]AAAGTACTTATTCAT | 57626 |
rs117547016 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764709 | CATCATTTGGGAACA[C/T]TTAGAAATGCAGAAT | 57626 |
rs117557939 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031888 | AACCTGACAATAGCC[A/G]GGAAAAGAGCAAGTG | 57626 |
rs117563009 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047764 | TTCCTCCTTCCTTGC[A/G]TGTTTGCAATTATAT | 57626 |
rs117565192 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831596 | CCTCTGTAAATCATT[C/T]TATGAAACTGCTATC | 57626 |
rs117573153 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923730 | CTAGAGCAGCTGCTG[C/T]GATGATGCCAGCTGC | 57626 |
rs117584108 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930792 | CAAACTAAGGCCATT[A/G]TAGAATTCATTCCTT | 57626 |
rs117586431 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748126 | AAGATTTATATATTA[C/G]TATCTTTTAATTAAC | 57626 |
rs117588917 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939648 | CCTGTTAAGTGTGCA[G/T]AAAGCCATAAAGAAG | 57626 |
rs117655975 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997419 | CTACAAGATGTTCAT[C/T]TTGCATAACTAAATA | 57626 |
rs117660601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086244 | GTTCTGAAGTTCGTA[C/T]CTCAGCCCCAGAAAT | 57626 |
rs117663104 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923326 | AAGTAATTTTGTAGC[G/T]TGGTGGAGGGTGACT | 57626 |
rs117670285 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939597 | AATCAGTTTAAATAA[C/T]TTTATTAATATCTAT | 57626 |
rs117674296 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843092 | TAAAGGGTAAAACTC[C/T]CAGTAAGATAGAAGG | 57626 |
rs117687320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763897 | AAAGTCTCCTCTGTT[A/G]TAACCCTTACAAAAA | 57626 |
rs117697759 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760718 | CTTTTTATAAAGACT[C/T]TTTTCAGGAGGCAAT | 57626 |
rs117708310 | snp | C/T | 0.421368 | 0.182025 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978547 | GTTGGGGTGCAGTTG[C/T]ACGATCTTGGCTCAC | 57626 |
rs117709721 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755544 | TACAAGCTTCTACTT[C/T]ATATTTGTTATATAT | 57626 |
rs117709838 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961858 | CTTGTGCCAATAAAA[C/T]AGTATTTTTAAATTA | 57626 |
rs117735667 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829649 | AAGCTACTCAACAAG[G/T]CGCCAGAGAAAGGTG | 57626 |
rs117745350 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732769 | GTTTTTCTAAGACAC[A/G]CCATCGGCTTCATTG | 57626 |
rs117750294 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779922 | TTCAAGTGATTCTCC[A/G]GCCACAGCCTCCGAA | 57626 |
rs117751329 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803030 | CCCACTGCTTCTCTC[A/G]ACCAGCCTTAAACAG | 57626 |
rs117754758 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894585 | CAACTTGAAACAATT[C/T]CCATATGAAATTGGG | 57626 |
rs117772842 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864261 | ATAATAGTCTGTGCT[A/G]TTAAAGCACTCATCT | 57626 |
rs117782166 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053700 | TTTTAGACTGTGTAT[A/T]GGCTACTTGATTTCT | 57626 |
rs117782782 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088230 | CAACAACAACAACAA[A/C]AAATAGATGCTCTGT | 57626 |
rs117794642 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971445 | ATCATCTTTGTCCTA[C/T]TTTTATGGTTTAATT | 57626 |
rs117819325 | snp | A/C | 0.031825 | 0.122064 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831096 | AAAAAAAAAATAACA[A/C]AGATCAGAGCAGAAC | 57626 |
rs117827946 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956705 | TACTTTTACCTCATT[C/G]ATTGGGCAGCATTAA | 57626 |
rs117837483 | snp | A/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69753841 | GGCATAGAAATAATT[A/G/T]AAAAAAAAAATTTTG | 57626 |
rs117864257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963594 | CAAAAACAAGCTGCA[C/T]AGCAGATGTGGCCCC | 57626 |
rs117877044 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766412 | AAATAGAGTACAAAA[G/T]GCATTTCATATATTT | 57626 |
rs117906070 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969402 | ATCCTCAAATATTTA[C/T]TACATACCAATTAGA | 57626 |
rs117917755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954154 | AATAAATGTCCAAGG[A/T]TCAGAATGAACACTG | 57626 |
rs117920606 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762003 | TATTACCATTTGATC[A/G]TTTAGACAGATTTCA | 57626 |
rs117922685 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807276 | TCTCCAGGCTCAAGA[C/T]ACTATTTTGAGAGTT | 57626 |
rs117932946 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908542 | AATTTGAAGAGAAAA[C/T]GTAAAAACCACTTTC | 57626 |
rs117955108 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931451 | ACTGCTTATTGGAAA[C/T]AAGCTCCCAACCTAA | 57626 |
rs117978269 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709700 | TAATTCAATAATGTT[C/T]TGGGTTGAAAACATG | 57626 |
rs117989626 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026013 | TTGACCTTCCATTTG[C/T]GGTAATCCAATATGC | 57626 |
rs118004269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799263 | TACTTCCCACAGACT[C/T]CAAAGCCTTGCTAAA | 57626 |
rs118029125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715857 | TCACAATAATATATC[A/C]AAATTGTTTTGATAC | 57626 |
rs118052221 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080531 | AAAATAATATATTGG[C/T]CAGTTACAATCATGT | 57626 |
rs118063044 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707081 | CAGGCTATGCAAAGC[A/C]CTTTCCTGTTTATTC | 57626 |
rs118063121 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901630 | ACATTTTAAAGGGTA[A/G]ATAGTGATCAAATTT | 57626 |
rs118068513 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710844 | AAGGTGGTGGGTGTG[A/G]GGTCTTACTGTATTT | 57626 |
rs118080826 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022589 | GAATTATTTTTAGAT[C/T]TGTTTTTAAATTTTT | 57626 |
rs118092626 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766743 | GATTAGATTCTCTTA[A/G]TGATATTTTTGGGTT | 57626 |
rs118095685 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813465 | ATAAAAAAATACACA[C/T]ATATATACACACACA | 57626 |
rs118097561 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016429 | AAGACCCCCTGTCCC[C/T]GTAGGCTCGTAAGTG | 57626 |
rs118126012 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081377 | AATTACACTGCTGCA[A/G]TCAAGATTTTGGGTC | 57626 |
rs118137290 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014196 | TTTTCTTCCTGAAGA[A/G]CTAAGACAAGAAAAA | 57626 |
rs118148908 | snp | A/C | 0.00951576 | 0.0683179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707617 | AATTATGCTGATGAC[A/C]ATCTTACCTGTGTCC | 57626 |
rs118156743 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829020 | GCTCTAAGGCCTTGC[C/T]CATTGCCTGAGAAAC | 57626 |
rs118173146 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051235 | GAAATTTTATTTAAT[C/T]GTAATTAGTAATATC | 57626 |
rs118192085 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761904 | ATGAGTGACTGTTCT[A/G]AATTGCTAAGATGGT | 57626 |
rs137866332 | in-del | -/TACAATTAATAC | 0.476918 | 0.104919 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960676 | TTTATTCTCTACAAA[-/TACAATTAATAC]TACAATTAATACTTG | 57626 |
rs137877987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844505 | TTGTGTTTGCATTTC[A/G]TCTCTGACAACTCTA | 57626 |
rs137882289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913474 | TCTGGCGGTGCACGC[A/G]ATGGGGAGACAATTG | 57626 |
rs137882514 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814422 | AATTAAACTGAAGAG[C/G]TTTGGCAAAGCAAAA | 57626 |
rs137884178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849018 | AATAAGTTAACCTTC[C/T]ACCCTGTATGAACAT | 57626 |
rs137885469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802448 | AGACCATCCCTCATA[C/T]TGTCTTATGCCCAAT | 57626 |
rs137888502 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918247 | GTAAATTTTATTTTA[A/G]AATATAATTAAATTT | 57626 |
rs137893007 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886324 | TTAAAATAATTTTTC[A/T]AGCTAAAACAATGTA | 57626 |
rs137898793 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978351 | GCAGACTGCATGATT[A/T]GGTTTTAAAATTCAA | 57626 |
rs137901115 | in-del | -/G | 0.0322114 | 0.122752 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830042 | AAACAATAATACAGT[-/G]GGAAAAAAAAAGAAG | 57626 |
rs137916598 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872890 | CCAATGACACAAACA[C/T]CTTTCATTAGGCCCC | 57626 |
rs137920979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053712 | TATTGGCTACTTGAT[A/T]TCTATTGTTGTAAAC | 57626 |
rs137940278 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010992 | TACTGGATAAACATT[C/T]TTGAGTTCTGGGGCA | 57626 |
rs137944035 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708501 | AACTTGGAGAAATAA[A/T]TATAACATGAACACA | 57626 |
rs137951077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780569 | CAAATATATACAAGG[A/G]TTGTATTATGCTGAT | 57626 |
rs137955903 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950686 | TCTTTTGGTCATTAT[C/T]TTAATTTAGGATACC | 57626 |
rs137972730 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747867 | AATCTAGCTTTCATA[C/G]AAATATGAAATATTT | 57626 |
rs137978695 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857041 | TCCTCCAATGAACAA[C/T]AGTAAATTCCGAACC | 57626 |
rs137980259 | in-del | -/ACTGGTGAACTTGGTACATAGTTCACCT/CACTGGTGAACTTGGTACATAGTTCACC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69935235 | GTACATAGTTCACCC[lengthTooLong]ACTGGTGAACTTGGT | 57626 |
rs137986739 | in-del | -/TCTATCTATCTATCTATCTATCTATCTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789018 | TGGACTCCACAGGAC[-/TCTATCTATCTATCTATCTATCTATCTA]TCTATCTATCTATCT | 57626 |
rs138007881 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70049171 | AAGAGACTATTAAAA[C/T]TCATTTGATAGATAT | 57626 |
rs138008444 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920276 | TTTTGGAAAACAGTA[C/T]ATGATTACTATAATC | 57626 |
rs138024916 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819673 | TCCTTCACTTGTCCA[C/T]TCAGTTAATCAGTAC | 57626 |
rs138037051 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754062 | GCCCAGGATGGTCTC[A/G]AACTCCTGGGCTCAA | 57626 |
rs138047929 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948953 | ATATCAATGTCACTC[C/T]AGAAATTCAAACCTC | 57626 |
rs138052734 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108721 | ACACATGAATCATGG[A/C]AGTGTAAACTTAATA | 57626 |
rs138064656 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957575 | TTTTCTAATATACAC[C/T]GTGACCCTCTTCATG | 57626 |
rs138070451 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860545 | AGTCTTAAATATGAG[G/T]CTGACTATAATCCTT | 57626 |
rs138090549 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017183 | AACACTGAAAGAGCT[G/T]TTACACAAACAGATC | 57626 |
rs138095692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727522 | GGAATGATTTGGTAT[A/G]GCTGGGACATCAGGT | 57626 |
rs138103043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932358 | TTTGTGGAAGACTGT[A/G]CTTTATAAGTTGAAA | 57626 |
rs138108515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890946 | ATTCAAATTATACAA[C/T]GAAGAAAAGTATTCA | 57626 |
rs138112528 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090491 | GAAAAAAAAAACAGA[C/G]AAGTTAAGAGTATTA | 57626 |
rs138120844 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854220 | TTGGCTCATAGTTCT[G/T]CAGGCTGTACAAGAA | 57626 |
rs138137544 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788919 | ATGATATTACAATGG[C/T]TATTACAAAAATGAC | 57626 |
rs138158288 | snp | A/G | 0.128288 | 0.218372 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782885 | GGGTCCCTGACCCCC[A/G]AGCAGCCTAACTGGG | 57626 |
rs138176136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060105 | CTGATCAAATATGGG[A/C]AAAAGATCTGAATAG | 57626 |
rs138180858 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990185 | GAAAGCAGCACTAAA[G/T]ATGGAAAGACCATTA | 57626 |
rs138185377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098381 | TTGCATGTATATTCT[C/T]TTGAAAACAGCAAAA | 57626 |
rs138194883 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827909 | CTTCAAATTCAAAAT[A/G]AGCTTGGAAAATACT | 57626 |
rs138205400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861116 | AATGGCCAAAGTAAC[A/G]CTAACTGGTAAATAT | 57626 |
rs138212526 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933039 | TGTACCCAGCCTGCC[A/C]CATTTTTACTTAGTT | 57626 |
rs138212788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992648 | TCTGGATACAGAATG[A/T]TCCTTTATCTTTCCT | 57626 |
rs138220088 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820156 | AGTTCTATTTCTCTA[C/T]ATCAAACTGTGTAAT | 57626 |
rs138221162 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990958 | ATACCAACCACACTC[C/T]TGGACCACGGAGCAT | 57626 |
rs138222707 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887107 | GGTCTAATGTTTTGG[A/G]TCTAAGATTTTAAAA | 57626 |
rs138228588 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936701 | AATGTTCTAAGTTTA[A/T]AAGATATGAATAGAG | 57626 |
rs138229739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953767 | ACATATAATAAATTG[A/G]ACTCAAAATTAATAA | 57626 |
rs138231165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724056 | TTGGCCAGGATGGTC[C/T]GAACTCCTGATCTTG | 57626 |
rs138234901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898750 | TAATACCTAGTGCCA[C/T]TGCCTCTTCTGACAA | 57626 |
rs138242564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060394 | AGAACTAGAATATGA[A/T]CTAGCAATCCCACTG | 57626 |
rs138243017 | snp | A/G | 3.29701e-05 | 0.00406005 | synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107457 | GGAGGAAGAGGACGG[A/G]GAGGACGATGAAGAG | 57626 |
rs138249385 | in-del | -/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039074 | TTTTTTTTTTTTTTT[-/TT]GTAATGGACAGGGTG | 57626 |
rs138259086 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69891710 | ATCAATTGATATTAG[-/A]AAAAAAATAATATTT | 57626 |
rs138280323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940982 | TTAGATGATTTTATT[A/G]TCATTTAGATTTACT | 57626 |
rs138285629 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996537 | TGTGAAGCTGTCAAC[C/T]TCCCATAACACTTTG | 57626 |
rs138286955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026808 | GCAGAATCTGAACTG[C/T]ATGTTAATGGATAAA | 57626 |
rs138295386 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776150 | GACAGAGTGAGACTC[C/T]GTCTCGGAAAAAAAA | 57626 |
rs138302063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102689 | TTCTAGGAAAATTAA[C/T]TACCCTCTTTATATT | 57626 |
rs138313695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834265 | AAGTACATAAATTGG[A/G]GGGAGAAAAAATGAA | 57626 |
rs138313946 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789287 | GTCTGTCTGTCTTTT[A/T]TTTTGTATGGGTAAC | 57626 |
rs138352699 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765801 | CTCCGATCTGTTGCT[A/C]AACAGAGAAGGAAGA | 57626 |
rs138353124 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800927 | ACTTGGAAGGGATTC[A/G]AAATGAAAGTTTACT | 57626 |
rs138357868 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69965381 | ATGTTACAATTGTTC[A/T]TGTTTGGCGGTGTCA | 57626 |
rs138366246 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872401 | GGTTAAAACTAGTTT[C/T]TGACAGATCCCAGCA | 57626 |
rs138374964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853627 | TGTGTAGATACATAC[G/T]GGAAGATAAGTGTTT | 57626 |
rs138376870 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007307 | AGTTTCTTCCAGTAA[C/T]TTTATTCTGCTCAAA | 57626 |
rs138378052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923329 | TAATTTTGTAGCTTG[A/G]TGGAGGGTGACTCTA | 57626 |
rs138391052 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907486 | GTTAATAACATTTGT[A/G]TTTATATGTAAATTT | 57626 |
rs138396045 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70105122 | ATAGTTTACACATGC[C/T]TAATCTCATAAGATA | 57626 |
rs138402941 | in-del | -/AT | 0.151721 | 0.239904 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841442 | GTTGAGAAAAAAAAA[-/AT]CAAGTAGTCCATTTT | 57626 |
rs138410459 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768610 | CTCTATGAAAAAATT[A/G]TACTGATTCTGCATT | 57626 |
rs138413132 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747214 | AGCTTACTCAGATAG[C/T]AGATACTCCATCAGG | 57626 |
rs138460129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806277 | GATAAATGTTTGCTT[C/T]TGTTCTCTGGGTCCA | 57626 |
rs138460521 | in-del | -/AAAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69753832 | TCCATAATGGCATAG[-/AAAT]GAAATAATTGAAAAA | 57626 |
rs138473010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907140 | GCAGTTGATAGGTTG[A/G]TAACATAGGTTCATT | 57626 |
rs138473326 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741017 | TTACTTACAACAATG[-/T]TACCTTAAAGCAATG | 57626 |
rs138473657 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973460 | CATAAAAATTATTTA[C/T]TTTTATATTATTTGA | 57626 |
rs138486848 | in-del | -/GGG | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756303 | CTAGTGCAAAATATT[-/GGG]GGATAAAATGGAATG | 57626 |
rs138497758 | in-del | -/TTTC/TTTTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884924 | TACCACTACAGCACT[-/TTTC/TTTTC]TTTTCTTTTCTTTTT | 57626 |
rs138504597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948646 | AGATATTTGAATTTA[G/T]ACTGCATTGACATAA | 57626 |
rs138508007 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797429 | TTTAAATTTGTCATA[C/T]GCCTTAAATAACTGA | 57626 |
rs138523660 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001605 | TCTATCTATCTATCT[A/G]TCTATCTATCTACCT | 57626 |
rs138524037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877266 | TTATGGGTATTTTTA[A/G]AATTCATACATAGTA | 57626 |
rs138529409 | snp | C/G | 0.148661 | 0.22854 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840250 | TTTTTTTGAGACAAA[C/G]TCTCACTCTGTCACC | 57626 |
rs138530191 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881687 | ATTTTTCTGTACCCT[A/C]CTTAACTCATCGATA | 57626 |
rs138534200 | in-del | -/AC | 0.479421 | 0.0993283 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045575 | TTTAAAAAACACACA[-/AC]ACACACACACACACA | 57626 |
rs138534831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950501 | TTTTCCACTCTCACT[A/G]ATTTCCATGGAGTTT | 57626 |
rs138544502 | in-del | -/CTTT/TTTC/TTTTC | 0.221141 | 0.248329 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884935 | CACTTTTTCTTTTCT[-/CTTT/TTTC/TTTTC]TTTTTTTTTTTTTTT | 57626 |
rs138549906 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969232 | CTTATAAGATTCATG[G/T]CTTTAAATATTTTAT | 57626 |
rs138549956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006584 | CTCCACCAGTGAAGC[C/T]ATTTGTCCTGGGGCT | 57626 |
rs138553073 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774080 | GTTTGTACCAAGTGA[C/T]GAAAAAATCCAGTTC | 57626 |
rs138563158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089980 | GACCCATAAACCCCA[C/T]TCATATTTTTACTGG | 57626 |
rs138563209 | snp | C/T | 3.29951e-05 | 0.00406159 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107354 | AGAAGAGAGTCCTGG[C/T]TGGCTGCTGAGTGCC | 57626 |
rs138570916 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978675 | TATTTTTAGTGGAGA[C/T]GGGGTTTCACCATGT | 57626 |
rs138574029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902559 | GGCATATATACACCA[C/T]GGAATACCATGCAAC | 57626 |
rs138581475 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011874 | CTGAGCAATTTACCA[A/G]AGAAAGATGTTTAAT | 57626 |
rs138583257 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857335 | ATTGACTACTCCTCC[C/T]TTTGTGCCTCCTATT | 57626 |
rs138599444 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981751 | TAAACAACATATAGT[A/C]ATTTTTACAAAAAAA | 57626 |
rs138611046 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754188 | GAGCTACCCTTTAAG[A/G]AATGATAGGATTATT | 57626 |
rs138636544 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782541 | GCTTGGAGGGTCCTA[C/T]GCCCACAGAGTCTCA | 57626 |
rs138641274 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732353 | CCTAAGCAGAAGAAA[G/T]ACAGAGTTGAGATCG | 57626 |
rs138650686 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086219 | GTTAAAATTATGTTG[A/T]GAGAGAGATGTTCTG | 57626 |
rs138663048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895634 | TTCTGCTTCAGGTTT[C/T]GCCAAGTGAAAATCA | 57626 |
rs138671547 | in-del | -/TTTG | 0.138546 | 0.223781 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919550 | TTTGGGTACATTAAT[-/TTTG]GACACCAATTTTCTC | 57626 |
rs138674164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054004 | TGGCCTTTGATGGCA[A/T]TTTGTTCCTCTCATT | 57626 |
rs138697207 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709764 | AAGGAAGGACAGAGA[A/G]GGCAGAAAAATGGAT | 57626 |
rs138703453 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818621 | TGGTTCTCCTCTACA[A/G]TATCCCTTAGCAAGA | 57626 |
rs138703746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761901 | TTGATGAGTGACTGT[C/T]CTAAATTGCTAAGAT | 57626 |
rs138704495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781943 | TTAAAGAGATGACAT[C/T]AATTGTAGATTTTTC | 57626 |
rs138707083 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722953 | ATGGATAATGGAAAT[A/G]TGCTCCATTTGTTGG | 57626 |
rs138708366 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890381 | TTAAATTGGAAACAT[C/T]CTTTGAAATCACTTA | 57626 |
rs138711352 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69903786 | AGCTGGGATTACAGG[G/T]GCGTACCACCATGCC | 57626 |
rs138730553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965260 | ACCAGTTTTCCAACA[G/T]CATGGGCTCACTTCA | 57626 |
rs138730802 | in-del | -/TA | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932043 | TATGATATCTAATTG[-/TA]TATTTCAAATTATTA | 57626 |
rs138734150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761200 | GTTTCAGAGTGACTC[C/T]GGGGCTGCCACATGG | 57626 |
rs138737140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715506 | ATAAATTACCCAGTC[C/T]AAGGCAGTTTTATTA | 57626 |
rs138764489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772692 | TACCGTGTGTAAAGT[A/G]TCTTGCAGGTAATAG | 57626 |
rs138768197 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741508 | AATACAGTTTATTAC[-/T]CATAGCAACAGCAAT | 57626 |
rs138768457 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063304 | CCCCTCCACAGACTG[A/C]ATGAATAACAAGTGC | 57626 |
rs138772046 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765370 | TATACTAATAGATAT[C/T]TTATACAAAATATTA | 57626 |
rs138772097 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720096 | CAACAACTTTCTTAC[A/T]CAGTGCCTATACTAT | 57626 |
rs138776715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865506 | ACATTAGGATTTAAT[G/T]TGTGTTTTTAAAAAA | 57626 |
rs138801195 | in-del | -/TGAA | 0.0584853 | 0.160693 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840089 | TACACAAATGTTCAT[-/TGAA]TGAATAAAAATGGCA | 57626 |
rs138805602 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023505 | TTAAGTTCATACTCA[C/T]ATTTTTCTAACTGCC | 57626 |
rs138806597 | in-del | -/T | 0.140581 | 0.224783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793597 | TTTTACTTTAGACTC[-/T]AGCTTCTTTTCACTT | 57626 |
rs138811199 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895947 | TTGTGACCTCAGGTG[A/T]TCCACTCACCTCTGC | 57626 |
rs138822569 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882113 | TAGGATTTAGATCCA[C/T]GATCCATCATCATAC | 57626 |
rs138824346 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989650 | TTGAGGAGTGTTTTG[C/T]AATTCTCATTGTAGA | 57626 |
rs138824450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927668 | TTGCTCAGTTTCATT[A/G]GACATAGGAAAATCA | 57626 |
rs138835850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886806 | TGTCTTACCATCTTA[C/T]ACTCTGTGACCATTA | 57626 |
rs138837483 | snp | C/G | 0.0170346 | 0.090782 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786458 | ACAAAATTCAACAAC[C/G]CTTCATGCTAAAAAC | 57626 |
rs138850842 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034043 | GCACTTCCCTAAATA[C/G]AGTCAAAAAATAACA | 57626 |
rs138851526 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993540 | TTCCCATTCCCTTAA[C/T]CATATGAAACTTTCC | 57626 |
rs138870770 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69994992 | CTTTGGTATCTATAT[C/T]AACAATGTACCAAAG | 57626 |
rs138887399 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093490 | AACAAAATCTATGTA[A/G]TTCCTAAGCACTTTA | 57626 |
rs138894645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936784 | TACTGAAGATTTCAA[C/T]CTTCATTTCAACATG | 57626 |
rs138899217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023047 | AAAGAATGTTCTTCC[A/G]TGTTTTTCAGTCACA | 57626 |
rs138907470 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968637 | GTGCATATGTATGTA[G/T]GTGTGCATGTCTGTC | 57626 |
rs138916663 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805684 | ACCAGCTCTAGATGA[A/C]AAAAAACAAAAAAAA | 57626 |
rs138920612 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700923 | GCTTCCATGCTTACA[C/T]TGAACTCAACATAAG | 57626 |
rs138935638 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025699 | ATATATATTATATAT[A/C]GTATACATATGATAT | 57626 |
rs138937474 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985416 | ATTAATCATCAGATA[A/T]ATGCAAATCAAAATC | 57626 |
rs138937966 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70090477 | TATTGAAAAAAAAAA[-/A]CAGAGAAGTTAAGAG | 57626 |
rs138943797 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102438 | ATCTTTGACTAAGGC[A/T]TATCTAGAATTTTTC | 57626 |
rs138954120 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030506 | CTACAAGGTACATAA[C/T]GAAATGAAGGCAGAA | 57626 |
rs138964920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923687 | GTTAGTGAGAGACAA[C/T]ATAGTACTGATGAAT | 57626 |
rs138973592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933428 | ATGGTTTATTAGCAG[A/G]GTTATTGGTCAAGAT | 57626 |
rs138977955 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075772 | CACATATATATATAT[-/TA]ACATATATATGTATA | 57626 |
rs138980771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741909 | CCTTGCTGCAAGCTA[C/T]AAAACTACTTTTTGA | 57626 |
rs138993233 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69776563 | TTTAGCATTCCATTA[C/T]CACATGCACATAGAG | 57626 |
rs138998103 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843660 | TGTTAGTGGTACAGT[A/C]AGTTATAAGTAATTT | 57626 |
rs139000425 | in-del | -/C | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825000 | TTCAATTTTGAAATG[-/C]ATTAAAAAATTGATG | 57626 |
rs139010546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796356 | TTTGGATCATGGGAG[C/T]GGATCCCTCATGAAT | 57626 |
rs139016010 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054464 | CCAATGGATATATAC[A/G]TAACATTGATTTTAT | 57626 |
rs139016172 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097296 | AAATAAAACTGAAAC[A/C]ACAAAAACAAATCCT | 57626 |
rs139026112 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780097 | ACAGGCATGAGCCAC[C/T]GTGCCCAGCCATTTT | 57626 |
rs139027079 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737999 | CAGGCTGGCATCAGG[C/T]TGGTGCCCCTCTGAG | 57626 |
rs139030670 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827371 | ATCTTCAGTAAAATT[A/C]TAAATAAAAATAATA | 57626 |
rs139069151 | snp | A/C | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064896 | TGTATGAAACTACCA[A/C]CCCATCTTACATTTT | 57626 |
rs139072461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036693 | TTCAATGAAGTAGGA[C/T]ATTCCCTTATTTAAA | 57626 |
rs139073156 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774641 | ATTCCTTTATTTTCC[C/T]AATAAACTTGCCTTC | 57626 |
rs139076708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969901 | AAAATCTCTTATTGA[A/G]GTCACTACAAATTTA | 57626 |
rs139084728 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798778 | AAAAATTAAGAGTTA[C/T]ACACAGATGGCCTGG | 57626 |
rs139101849 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69728936 | GTGGTACTACATATT[C/T]ATTAAAATTCAAGCC | 57626 |
rs139109946 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792308 | ATACAAAAAAGATTC[C/T]CAAAAATAATTAGAA | 57626 |
rs139110629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866582 | AAAGCCAGGGATTCC[A/G]CGAGTTAGAGTTAAG | 57626 |
rs139116375 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938297 | AATAATTTGAAATCA[C/T]TTAAATTTCAGCAGA | 57626 |
rs139116726 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099677 | TAAAAAGAAATACAC[C/G]ATACAATAAGCTTTT | 57626 |
rs139147490 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808047 | AAAGTCCACCATAAG[G/T]TAATGAAAATGCAAG | 57626 |
rs139154621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878357 | GAATTTTGTAAGCAG[C/T]CCACATTGAGTCTTT | 57626 |
rs139154758 | in-del | -/GGCACATATTTGA | 0.379942 | 0.213577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068487 | TATTTCTTATACAGT[-/GGCACATATTTGA]GTTTCAGACCCAAAG | 57626 |
rs139158751 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078686 | TCCAGCTGATCTTTG[C/T]GACCACTGCCAGCTC | 57626 |
rs139166476 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733860 | ACAGCCAGCTAAAAT[A/G]TGTATGTACATTCAC | 57626 |
rs139170267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794115 | TTAAGCTACCAGCTC[C/T]AAGGTTAAGGCATCC | 57626 |
rs139177120 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703970 | ATGACTGTATATGTT[C/T]ACAAGCCCTATCACT | 57626 |
rs139183362 | in-del | -/C | 0.0733688 | 0.176922 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730588 | CATTCCTTTTTTTTT[-/C]CTGGATACAGGATCT | 57626 |
rs139185722 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094952 | TAGAATAAATACCAA[C/T]GGCTATCTTCTATAC | 57626 |
rs139208405 | in-del | -/AT/ATAT/ATATAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69736679 | TAAAGAGATTGTGAG[-/AT/ATAT/ATATAT]ATATATATATGTATA | 57626 |
rs139217890 | in-del | -/TC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70036834 | ATTTTAATGCCATGG[-/TC]TTTTTTTTTTTTTTT | 57626 |
rs139231310 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954679 | TGGCACAAAGCCAAA[A/G]CACTGTTCAATAACA | 57626 |
rs139235019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908226 | GAGACGCCAGAACCA[C/T]GGGGGTTAGTGTGGA | 57626 |
rs139236120 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001294 | TAACAATTCAAAATT[A/G]TTTGACTTACGAATT | 57626 |
rs139236787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096423 | TCATTATAGCTTTGA[C/T]TTATATTTCTCTGAT | 57626 |
rs139244111 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832847 | AGGAAACAAAAACAT[A/G]GAGTGGGGAAAGGAC | 57626 |
rs139245438 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980122 | AACAGTTCAGGACTC[A/T]ATATTCTTTACTCTC | 57626 |
rs139255875 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902254 | AGTTTTAAATTTCTT[C/T]CATGTTTGTTCAACA | 57626 |
rs139259486 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851166 | TACTGTGTTTACTTA[A/C]ATTTTATGCTTGAAA | 57626 |
rs139260966 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945549 | TTGCAAATCATATCT[C/G]ATAAAATATTATATA | 57626 |
rs139265354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874952 | TCAGAAGAAATTTAG[G/T]ACTACAGGTAAATTG | 57626 |
rs139285681 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004128 | GGTATGTATGAGAAG[C/T]TTTTAACTGATACTC | 57626 |
rs139314617 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039976 | TTTCCAGTGTAAATC[C/T]TTCTGTAACTCTCTT | 57626 |
rs139315428 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836874 | AAAATGCAATAATTA[C/G]AAGAGAGGTATTAAT | 57626 |
rs139324295 | in-del | -/A | 0.0901694 | 0.192235 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824654 | TAGATAAAAGACTAC[-/A]AAATGTGTGATTTCC | 57626 |
rs139327537 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087390 | AGGCATGCAAAGAAT[C/T]TAACAGTCAACCAAG | 57626 |
rs139348728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984107 | TGGGCAAGGACTTTT[C/T]TGGATGAGATCTCAA | 57626 |
rs139348765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730360 | AGGATACTTCTCACC[C/T]ATATTAGGCAAATTT | 57626 |
rs139352929 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043214 | CAGCCATGTGTCTTA[C/T]ATTTTAACAAACAAG | 57626 |
rs139354376 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820713 | TTCAGGCCGAATTTG[C/T]TCTGCATACATCAAA | 57626 |
rs139358653 | snp | C/T | 0.00427359 | 0.0460481 | synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107601 | CAGGCAGCCTCCCCC[C/T]GCCGGGCCGCCGGTG | 57626 |
rs139366197 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042078 | CAGGCTTATCCTAGG[C/G]CTTCTTTTTTCCCCA | 57626 |
rs139382414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718191 | GAAAATTTTTCTGCT[A/G]TCAGTGCTATCAGCT | 57626 |
rs139387037 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941507 | CTATATCAAAAAGTC[C/T]GAAAGAGCACAAATA | 57626 |
rs139387932 | in-del | -/AAC | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055023 | ATTCAAAGACGTAAT[-/AAC]AGAAATCTTTCCAAA | 57626 |
rs139392850 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770135 | CCCCTTGGGACTCCA[A/T]GATGGCTGGAGTCTC | 57626 |
rs139407571 | in-del | -/A | 0.117537 | 0.212022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043239 | ACAAGTTTAAATACT[-/A]AAAAAAAAATAAAAA | 57626 |
rs139407742 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897227 | GACTCCCTGGCCAAA[C/T]TTAATCTCTGAGTCA | 57626 |
rs139408450 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109385 | AGAATATGGTTGTTG[C/T]CCATTCATGAAATTC | 57626 |
rs139411344 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993887 | TTGAAAGCCTAACAT[A/G]TTTGAGAAATATAGA | 57626 |
rs139429998 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091808 | AGGTGCCGCCTAAAC[C/T]ACCTTAGAGCTAACT | 57626 |
rs139431305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934226 | TGGTGGTAAGGCTCG[C/T]CATCAGTAAAGCTGC | 57626 |
rs139433001 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020096 | AGCCTTCATAAATGT[A/G]AGAAATAAATTCCTG | 57626 |
rs139445129 | in-del | -/TA | 0.105214 | 0.203807 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013628 | GTGAACAAAATGAAT[-/TA]TATGTTTCCTTAGAA | 57626 |
rs139458949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998561 | GGTCTAGAAGTAAAT[C/T]ACATGGAAATGTAAC | 57626 |
rs139459083 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943024 | AAGAATCCATACTAG[C/T]TGTTCTGCAGAATTC | 57626 |
rs139459292 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044987 | CCAAGTTATCTTGTC[A/G]TGAAAAGGAAACAGC | 57626 |
rs139473263 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859068 | TTTTCATTCAACACA[G/T]CAAAGCACTGTATAA | 57626 |
rs139473734 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899296 | GTGTGCACAATATGA[C/T]GTGCAAATCAGTTAG | 57626 |
rs139493477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739292 | GTTACCAGCCGCAAC[A/G]AAAACACACTTAACT | 57626 |
rs139497740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998154 | ATTTACCAATAAGCT[C/T]ACTGGTCTACCACTT | 57626 |
rs139501811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802662 | TTCCAATCTAATTAC[C/T]GGTGCATGCAGCCCC | 57626 |
rs139501894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754833 | ATTTTGCTATTACCC[A/G]AATGTTCCCTGAATT | 57626 |
rs139502675 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942611 | AAACCTATAATAATT[C/T]GCAAAACCCACCCAT | 57626 |
rs139507472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105989 | TTAAAATTAAAAAAT[A/G]TATATAATGTATATA | 57626 |
rs139510062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815661 | AAACCTCAGCATCAC[A/G]CAATATACCCATGCA | 57626 |
rs139514879 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100574 | TCTTGACCTCACGAT[C/T]CACCAACCTTGGCCT | 57626 |
rs139532342 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829568 | CACACTAGCTCACCA[A/G]CAATGGATCCAAACC | 57626 |
rs139535117 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061140 | ACCTCTATGGTATAT[C/T]CTCTACTCACTTAAT | 57626 |
rs139537212 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900679 | TTGGAAGAGACAGAC[A/G]TCATGGACAGAGGGA | 57626 |
rs139558732 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041409 | GGGTGAAGGTGGCAC[C/T]AACTTTTTATTTCCA | 57626 |
rs139566324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757834 | TGGTGGCAGGTGCCT[G/T]TAATCCCAGCTACTC | 57626 |
rs139566734 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711095 | ATTAATTTTTCAAGC[A/G]TTAGTGTCATTTTCA | 57626 |
rs139573314 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845134 | TACCACAGTGCAAAG[C/G]CTGCTTTAAAATAAC | 57626 |
rs139580435 | snp | A/C | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109066 | CAAGAATGGAATAAA[A/C]TGATAAAAGAGAATT | 57626 |
rs139584699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751324 | ATGCCTTCTATAAGT[C/T]CATACCCTCACAGAA | 57626 |
rs139590920 | in-del | -/C | 0.392696 | 0.205275 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802674 | TACCGGTGCATGCAG[-/C]CCCCCAGTCCCGTAC | 57626 |
rs139600154 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070203 | AATAATTATTGCGAA[A/T]TTTCTAAAGTTAATG | 57626 |
rs139604873 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745317 | TCTTATTATTAATTA[C/T]ATCATTTTATCAATT | 57626 |
rs139609862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995867 | AAACTGTCACAATTC[C/T]CATATTGAGGTCTCG | 57626 |
rs139611555 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945823 | ATTCTGCTCCTAGAT[A/G]TTTGCTCAAGAGTAA | 57626 |
rs139638142 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858166 | ACATTTCAGCCATGT[C/T]GTCCAGGACCCAGAG | 57626 |
rs139640275 | snp | C/T | 0.0228947 | 0.104514 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110215 | GCCTATTTGTTAGTC[C/T]TGTAGTAACATTTAG | 57626 |
rs139651093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782178 | AAAATATAGTATTGG[C/T]TGGGGAGTCAAGATG | 57626 |
rs139651177 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739438 | GGGCTAAATGCCCCA[A/G]TTAAAAGACACAGAA | 57626 |
rs139654012 | in-del | -/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934733 | ACCATCCCATCTACC[-/T]TGAATTTCATTAAAC | 57626 |
rs139657229 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850758 | CCATGTACTACAACT[C/G]AAAGTATTTCCTAAT | 57626 |
rs139668156 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924243 | AGGGGTAGGTACCTG[A/G]TGAAATCCCACCTTC | 57626 |
rs139672846 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023679 | CCCTGGTTGACTTTG[A/C]TGAATCAATCATGAC | 57626 |
rs139682411 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009613 | AAAAGAAGTATGGAC[A/G]TTGAAATATTGGCTG | 57626 |
rs139684008 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103375 | ATTGTCATCAGTTGG[C/T]GTCCATAGTATAAAC | 57626 |
rs139697396 | snp | A/G | 0.097727 | 0.198275 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812401 | GGGAATACCATTCAG[A/G]ACATAGGCATAGGCA | 57626 |
rs139705217 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910380 | CATACTAGTCATTTC[C/T]TGTCTAATTTTGACT | 57626 |
rs139712475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743937 | TTGGGGAAAGCTTGA[G/T]AACTCTATTTTGGAT | 57626 |
rs139716573 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720386 | ACTTATCCATTTGCT[A/C]ACTACATATTTTTGA | 57626 |
rs139718548 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750690 | TGCTGATCATGGGCC[G/T]AACACAATGTAGTGT | 57626 |
rs139724271 | in-del | -/ACCC | | | frameshift-variant | KLHL1 | GRCh38.p7 | 13:69796869 | GTTTGTCATCAATAA[-/ACCC]CAGCCACACCAAACT | 57626 |
rs139734550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060560 | AAAAATGTGGTATAT[A/C]TAGGCCAGGTGCATG | 57626 |
rs139738024 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779073 | AAAGTGCTGGGATTA[C/T]AGGTCTAAGCCACCA | 57626 |
rs139754156 | in-del | -/ATTTTGAAA | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827087 | AATATGTTACGTTAG[-/ATTTTGAAA]ATTTTGAAAACATGT | 57626 |
rs139781949 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063877 | CTTATATTATATTTA[G/T]AGGTGTGTTTATATG | 57626 |
rs139784403 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955692 | AGCAACTTTAAAATA[C/T]AGTGAACCTCAGTGC | 57626 |
rs139799398 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846243 | TTAACAACTCTGTCA[G/T]CTAGGTGGTCACTTT | 57626 |
rs139805957 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69770369 | AAGCTTTGCTGGCCA[C/T]GGAGGTTTCTGGCTT | 57626 |
rs139820029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957777 | CTAAGATCACAAGCA[G/T]ATTTTCTAGTAGAAA | 57626 |
rs139825101 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915954 | GAACAGACACTTCTC[A/G]AAGACATTTATGCAG | 57626 |
rs139837998 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730911 | ACTATTATTGTAAGT[C/T]TTACTATCCATGAAT | 57626 |
rs139852145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767027 | CCCATATCAAAGTAG[C/T]AATTGGTATTTTTCT | 57626 |
rs139854908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018296 | TAAATGGAAGATAAA[A/G]TAAATTGTCCAATGT | 57626 |
rs139857946 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70015317 | CTGAATACTGTGGGC[A/G]ATTTTAATATAAAGG | 57626 |
rs139873926 | snp | C/T | 0.081446 | 0.184634 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786878 | ACAGACAAACAGAGC[C/T]GAATCATGAGGGAAC | 57626 |
rs139880817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873114 | TATAGGTCCAAATTC[C/T]TCCTTGCCGGAATGT | 57626 |
rs139882258 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858692 | GAAAATTTTTCTATT[A/G]GTGGAAATGACTATT | 57626 |
rs139891015 | in-del | -/TCTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70098047 | AAGCCTAGATAAAGC[-/TCTG]TCTAATGGAGGCTTG | 57626 |
rs139892862 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920546 | TAATTAAGAAAACTA[C/T]ATTGAGGAGCAATAT | 57626 |
rs139898851 | in-del | -/A | 0.165853 | 0.235413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893181 | AATAGTATACTCTAT[-/A]AAAAAAATTGGAATA | 57626 |
rs139912382 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975262 | CATTTCAGATTTTAG[A/G]CACAATTCCTGAATT | 57626 |
rs139916031 | snp | A/G | 0.000281329 | 0.0118569 | missense | KLHL1 | GRCh38.p7 | 13:69961340 | ACAAGGTCCCAGAGA[A/G]CATTGGGGTCTATGC | 57626 |
rs139919690 | in-del | -/AAAC | 0.0737376 | 0.17729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773046 | CATTACACAGGCAGA[-/AAAC]AAACAGAACAAGCAA | 57626 |
rs139924872 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799138 | TGTCTCTTGTGACTA[C/T]ATTTGACCGATGATG | 57626 |
rs139935360 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010065 | TGAGAATTCTTGGTA[C/G]TTTCAAAACAAGGAA | 57626 |
rs139946682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069439 | TATGTCTTTTAACAA[A/C]AAATTACAAGGCATG | 57626 |
rs139949007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079324 | GCATGGCATTTACCA[A/C]TTGTTACAGTTCAAA | 57626 |
rs139952219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717780 | ATTTTTAAAATAAAT[G/T]ATTGCACATTTGTGA | 57626 |
rs139954984 | snp | C/G | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995470 | TATTATGCTCTCTCT[C/G]CAAGTTATTTTATTT | 57626 |
rs139972314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971094 | TATTTCAGTACCCAG[A/C]TTGCCTGGGTTTGAG | 57626 |
rs139993384 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904856 | TGATTCCTTTAACTG[C/T]CTTGGAATCTTCATT | 57626 |
rs139994178 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081249 | CTTTCTACTGTTGTA[C/T]AGTGCCTTACTACAA | 57626 |
rs139997379 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008654 | CACAATTATTCTCCT[C/T]ACATCTTTTTCCTCT | 57626 |
rs140013200 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717887 | GGACTAGAAAATCTT[A/C]AAGTGAAAATGCAGC | 57626 |
rs140015165 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783460 | GGATAACTAGAATAA[C/T]CAAAGCAGAGAAGTC | 57626 |
rs140026038 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055670 | TTTAAAAAGTGGCGA[A/G]TATGTAGTGAAAGTG | 57626 |
rs140026894 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952013 | TTATTTCCCCTCTTG[A/G]ATAGTGCACTTTGAA | 57626 |
rs140035375 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69962680 | GTTAATGATATTTTA[G/T]AATGAAAAAAATTAT | 57626 |
rs140056481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927243 | GTTACACCTTTACTT[C/T]ACACCATATAAAAAT | 57626 |
rs140060159 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782279 | TCCATCTGAGGTACC[A/G]GGTTCATCTCACTAG | 57626 |
rs140062963 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820599 | AGAAGTGAAATTTGA[A/G]TAGCATCACAGACTT | 57626 |
rs140065736 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69758998 | TCTGGGTCCCAAGAG[C/T]TTACATGGCACCCAT | 57626 |
rs140079001 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865914 | TCTGCCCAATTTTAT[A/G]TGTATTTTAACATAT | 57626 |
rs140085969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764134 | GCCTGAAGCTGCTTC[C/T]GTGCATATTTTAAGT | 57626 |
rs140095282 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892991 | ATGAATAATTTACTA[G/T]TTGCTTACAACCAAC | 57626 |
rs140098097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722121 | CCTAGCACAGCTCTC[A/G]TACATAGTTTATAAA | 57626 |
rs140103027 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084909 | ACAAGATCTAAAACG[C/T]GGAATTTTGAAGCAA | 57626 |
rs140106992 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813424 | CACATGTATACATAT[A/G]TAACACACCTGCATG | 57626 |
rs140107541 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930417 | ATGCACACCACATCA[C/T]TGGTCACTTAAAAAC | 57626 |
rs140108385 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051697 | GCAGGAACATTACTA[A/T]GACTAGATGTGTGGA | 57626 |
rs140121861 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991497 | AATGACACAAGAGAC[A/G]TTACCACTGACCCCA | 57626 |
rs140130826 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763042 | CTTCTGGATGGGCAT[C/G]CTTTGTTAGGTTTCT | 57626 |
rs140140336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888430 | ATACTGGATTGGGGT[A/G]GACCATAATCTAATG | 57626 |
rs140155912 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095760 | CATCCCATTGTGCTA[C/T]TTAACACAGCATCTT | 57626 |
rs140161183 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024721 | AGGAGGGAACAATTA[C/T]GAACGGAAGTTGGAG | 57626 |
rs140161512 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734935 | CATGCCATGATGTTA[G/T]GCTAAAATAAGATTT | 57626 |
rs140166010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966401 | AGCACATCGTTTGCA[A/G]AATGGCTTACTGAGT | 57626 |
rs140175979 | in-del | -/ACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70055022 | TATTCAAAGACGTAA[-/ACA]TAGAAATCTTTCCAA | 57626 |
rs140201854 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099093 | TGGTAATAAATATTA[A/C]AAATATGGAATTTTA | 57626 |
rs140203526 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926231 | AGAGTCAAAGGGTGG[C/T]ATATTGCCCACACCT | 57626 |
rs140219960 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950618 | AGTTATTTAAATCTT[C/T]ACTTAAGTAACATAA | 57626 |
rs140222972 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989101 | GTTTTATGTTTTACA[C/T]TTAAGTCTATAATCT | 57626 |
rs140238879 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025302 | CTTAACCAAAACATA[C/G]GCTGTAATTCTCAGT | 57626 |
rs140245693 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057824 | AGAAAGAAAAGAAAA[A/G]CAAAGAAAAGGCCAA | 57626 |
rs140254711 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934835 | TCTACACCTGACTAA[C/T]TCTACCTCATTTTTT | 57626 |
rs140255654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860010 | CCTGACTTATTCACC[C/T]GTTACAAATTCACTC | 57626 |
rs140269972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731676 | GATTGAATTGACAAG[C/T]AGCTATTTGCTTTAG | 57626 |
rs140279493 | in-del | -/AAT | 0.14665 | 0.227637 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837561 | GTATATTTGTATATA[-/AAT]AATATGTATAGATAT | 57626 |
rs140286088 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969570 | ATCTTATGCATAAAA[C/T]GTATATAGTTGCAGC | 57626 |
rs140287330 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092450 | ATATTAAACTCTGTC[A/G]TCTTTGCTTAGGTAT | 57626 |
rs140288743 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70014995 | CATTAAGCAAACATG[A/C]AAAAATTATTAAAAA | 57626 |
rs140288980 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767439 | TGGTAACTCATGCCT[A/G]TAATCCCAGCACTTT | 57626 |
rs140298866 | in-del | -/G | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998349 | TAGAGCTCACACAAT[-/G]GGAGCTCCCATTGTG | 57626 |
rs140299816 | in-del | -/AGTG | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827447 | AAGTCATTCTTAGTG[-/AGTG]TCAGGGCATGGTGGC | 57626 |
rs140310961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984700 | CTTTTGCCTATTAAA[A/C]CTCCGCTCTTAACTT | 57626 |
rs140312627 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866047 | ATAAGTGACTACTCA[C/T]TGAAACAAGAGTTCA | 57626 |
rs140319346 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818888 | AATATGAAAAAATAA[A/C]CCTTCTTTTATTATA | 57626 |
rs140319716 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901643 | TAAATAGTGATCAAA[C/T]TTTTGAATGTTGACC | 57626 |
rs140320058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937696 | TATTTTGCATGATTC[A/T]TTGCCAAGCTGAGTC | 57626 |
rs140340014 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830271 | ATATTCCATGCAAAT[A/G]GACACCAAAAGTGAA | 57626 |
rs140343380 | snp | A/G | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726299 | TCCAGTGCCTTTGAA[A/G]AAACTCTCTAGATCC | 57626 |
rs140345191 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090051 | ATAATAGAATTAATC[A/G]TCATAGAATCCTAAC | 57626 |
rs140346144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791403 | ATATTTAAATCCCAG[G/T]TACCCTTTTGTAGAA | 57626 |
rs140352006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071880 | ACCTAAAATTAATAA[C/T]CTATTCTTCAGCCCC | 57626 |
rs140370798 | in-del | -/TCTA | 0.0754357 | 0.178962 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780022 | TTGGCCAGGCTTGTC[-/TCTA]TCTATCTCCTGATCT | 57626 |
rs140373130 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996258 | CAGTGAGCCAAGATC[A/G]CACCATTGCACTTCA | 57626 |
rs140408878 | in-del | -/AA | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927282 | GTGAATCAAAGAGCT[-/AA]AAATATAAGAGCCAA | 57626 |
rs140409628 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799644 | TGACAAATAACACAG[A/T]TTTGTTATCTTACAG | 57626 |
rs140409642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059527 | CAAAGCAAAAATGGA[G/T]AAATGGGATCATATT | 57626 |
rs140410221 | in-del | -/A | 0.0486741 | 0.148216 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772379 | TCATTTTTGTTGGGG[-/A]AAAAAATAAATCAAG | 57626 |
rs140411636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871454 | GATTGCTCCACAGCA[C/T]CCTTGGATTCTTCTT | 57626 |
rs140447406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031989 | TTTAGGTTGAGAAAG[C/T]CCTGGGGGTGAATCC | 57626 |
rs140452430 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897919 | CTGAGTCCAGTTAAA[C/T]CTCAGGAACTCAGGT | 57626 |
rs140474858 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898472 | CAACACCTGGCACTA[A/G]GATGCAGGGAAACAA | 57626 |
rs140477681 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973265 | ACCAGCACATAAATA[C/G]ATGATATTATGTAGA | 57626 |
rs140482310 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965269 | CCAACAGCATGGGCT[A/C]ACTTCATGTATCTTG | 57626 |
rs140486064 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704489 | GCTCTTACCAATGAT[A/G]TTCCTTAAGCCAAAG | 57626 |
rs140486165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998863 | ATTTTGTTGGAAAAG[A/T]CATTTTTTTGTGTCT | 57626 |
rs140489494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774808 | GAACTGACTACCTAT[A/G]TGTTATCTTTTATTG | 57626 |
rs140499138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940728 | TGTTTAAAATTGTCT[A/G]TAATTTTGGTTTTTA | 57626 |
rs140514851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775807 | GCAATTCTCCTTCCA[C/T]GTCACGGAAAGGGGC | 57626 |
rs140527891 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071194 | ATTAGAAGTAAGCAA[C/T]GGGGAAAGATATACC | 57626 |
rs140530102 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922585 | ATTTAAGAAAAGTAA[A/C]TAATAAAATGTTATT | 57626 |
rs140548008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703068 | TGATTTTCATGGATT[A/G]TCTCACATCAGAGTC | 57626 |
rs140554332 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778891 | ACAACTTCCACCTTC[C/T]GGGTTCAAGCAATTC | 57626 |
rs140559842 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809867 | AAGAAAGGTGTACTA[C/T]GCAAATGGAAAAAAA | 57626 |
rs140563805 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879100 | ACACCAGGGCCTGTC[A/G]TAGGAGATACGAGTT | 57626 |
rs140580327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808758 | TATAGAATTAAGAAT[A/G]TGGATAGCAAAAAAA | 57626 |
rs140581076 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69978071 | CACAAGTTCGCAAAT[G/T]ACAACCCCAGAATAT | 57626 |
rs140589505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708213 | AAGTTTCCTTTAAAC[A/C]AGTTCTGAAAGTCTA | 57626 |
rs140589724 | snp | C/T | 6.60306e-05 | 0.00574551 | missense | KLHL1 | GRCh38.p7 | 13:69719390 | ACATAATCCAGTAGC[C/T]GGGAACAGTGATTTG | 57626 |
rs140606325 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107090 | CCAGGGTGGCATCTC[G/T]TAACCCACATTTTCA | 57626 |
rs140626172 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073929 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 57626 |
rs140631432 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996471 | ATTGAAGCTGATACT[A/C]CAGATGTGATATTTT | 57626 |
rs140638749 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852401 | TCTTCAGGACAGCAA[C/T]TGAAGAGACAACATT | 57626 |
rs140642281 | snp | G/T | 0.0854556 | 0.188216 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878709 | ATGCATATATATATA[G/T]ATAGAGAGAGAGAGA | 57626 |
rs140655235 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837671 | ATGTGTGTGTGTGTG[-/TA]TATATATATATATAT | 57626 |
rs140659146 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742353 | TTTTAAATATATTCC[A/G]GAAAAAAGGACACTC | 57626 |
rs140661615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889560 | TCTTACTTTGACCTA[C/T]GTAACATATATGCAC | 57626 |
rs140666110 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104420 | ATAATTTGACCTTTC[C/T]AGAATTCTGAGATTG | 57626 |
rs140671896 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956783 | AAACAGACCAACACA[C/T]TTGTGATCTATCTCA | 57626 |
rs140672984 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949416 | GATTATTAGACTGGG[A/G]TTATGAATGAAGTTT | 57626 |
rs140690344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724709 | ATCTTGATTAAAGCC[A/G]TACATACACCACATG | 57626 |
rs140694237 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790237 | TAATAATAAGAACAC[C/T]GGCAAAAAAATATTA | 57626 |
rs140701524 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69986208 | AAGAATGGGAAGAGA[C/T]TGATCAATTGATACA | 57626 |
rs140704618 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885546 | GTAGGTTCTGGAAAT[C/T]AGTTGTTTTAACATC | 57626 |
rs140708664 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69952835 | TTACAGAAGTCTTAA[C/G]AAGGGTGAAATGACA | 57626 |
rs140721987 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047113 | AATAGCATTAATGTG[C/G]ACTGACCACTGCAGA | 57626 |
rs140725751 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782422 | CCTAGTCAAAGAAAG[C/G]GGTGACAGACGGCAC | 57626 |
rs140727885 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852947 | CCTATGCCAGACACT[G/T]TGGAGTGTGCAAAGA | 57626 |
rs140728938 | in-del | -/TTAC | 0.17138 | 0.237316 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954925 | TTGATTTTATTTTTA[-/TTAC]TTTTATTTTGTTACT | 57626 |
rs140731041 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882740 | TGCTGAGCTTTGTTA[G/T]GCAGGCAGAATGTAC | 57626 |
rs140731448 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780211 | ATACAAGCATGCATT[A/G]TTGAGAGACTTAACT | 57626 |
rs140738517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951708 | GCTCTATCTTGGTTT[A/C]CAAAATATGCTTCAT | 57626 |
rs140739659 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848554 | GGCCAAATTATTTAA[G/T]AATATTATTTATATT | 57626 |
rs140765706 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918579 | TACACACTTAGTTAA[C/T]GGCAGCTAACTGCAG | 57626 |
rs140768731 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045685 | TCTTATAAACACATA[C/T]GGAGTTTTAAAGAAA | 57626 |
rs140790054 | in-del | -/TG/TGTG/TGTGTG/TGTGTGTG | 0.435422 | 0.271137 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047399 | AAATGGAAATCTGTT[-/TG/TGTG/TGTGTG/TGTGTGTG]TGTGTGTGTGTGTGT | 57626 |
rs140800225 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992019 | ATGCAAAGTACTAGG[C/T]ACCACCTCAGACCTA | 57626 |
rs140803153 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823402 | CCAAAGGTATTTGGG[G/T]TTGTTGGTGAGGCGT | 57626 |
rs140814780 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092380 | TTACTCCATTTAGAA[C/T]GTTTGATTCACTACT | 57626 |
rs140819045 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732003 | ACTTTAAAGATGATA[A/T]AGACTTGACAGATAC | 57626 |
rs140825389 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981284 | TAAATAAATAAGATA[C/T]ATTAATTGCAAACAA | 57626 |
rs140825497 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021627 | ATTTTGTATTCCCAT[C/G]AGCAATGAATGAGAA | 57626 |
rs140835479 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053901 | AGGGAATGCGTCTAC[C/G]TACTTTCTTGCTGCT | 57626 |
rs140859307 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051231 | TTATGAAATTTTATT[G/T]AATCGTAATTAGTAA | 57626 |
rs140867954 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69771435 | TAAATTTTTTAGAGG[G/T]ATGCTGAAAGGTTGA | 57626 |
rs140878941 | in-del | -/AAA | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724421 | ACATCAGAAACACTT[-/AAA]GAAGAATTAATACTA | 57626 |
rs140880233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103803 | ACAGAATAGGAATTA[C/T]AAGCTCAATTTTGTA | 57626 |
rs140893805 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721988 | GAACCTCACTTACTT[A/C]TGTTTCATTTAAATT | 57626 |
rs140898137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093262 | GAAAATCAAGAACCC[A/G]TCATCATAGTGGAGT | 57626 |
rs140901179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837370 | AATAATAATTAGTAA[A/G]CAATTTGAAATGTCT | 57626 |
rs140908702 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936506 | GGACAGGAGAATTGC[C/T]CGAACCTGGGAGGCG | 57626 |
rs140919563 | in-del | -/AATGTAT | 0.030278 | 0.119257 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707460 | ATAAAAGTACACAAG[-/AATGTAT]AATGAACTTTTTACA | 57626 |
rs140931826 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089730 | TTTTTGGCTTTAAAA[A/C]CAATATTAGGTATAT | 57626 |
rs140938976 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088329 | TGATAATGATCCTTC[C/T]TCATAGGAGAGCTTT | 57626 |
rs140942263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016430 | AGACCCCCTGTCCCC[A/G]TAGGCTCGTAAGTGC | 57626 |
rs140943844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106974 | GTAAGTTCAATTGGT[C/G]GCTACAACTTTGAAA | 57626 |
rs140961503 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867017 | ATATTAACTCTAGGC[C/T]ACTTCAAGTGCCAAA | 57626 |
rs140966232 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999568 | TAAGTAAGAGATTGG[A/G]ATGATTAATCCCAAT | 57626 |
rs140974418 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741159 | GCTAAAATTACTAAA[C/T]ACAAGCAATTAAATA | 57626 |
rs140984545 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101897 | TATTATTTTTGCTAG[C/T]TTTGGTTTAAATAAT | 57626 |
rs140987265 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763869 | AGAAAACAGGAGATT[C/T]CAGCATAATAAGAAA | 57626 |
rs140989246 | snp | A/G/T | 3.68367e-05 | 0.00429153 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107626 | CCGGTGGAAGGAGAC[A/G/T]GGTGGCTGAAGAGTT | 57626 |
rs140994166 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967913 | AAAGAAATAAAAAAG[A/G]ATATTACACAAACTT | 57626 |
rs141006059 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760218 | CTCTGCCTAGACTCA[A/G]TATGGATAACTGAAA | 57626 |
rs141006158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794661 | AAATAGGAACAGTAC[A/G]TAGCCTAACAGAGAT | 57626 |
rs141015506 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69813517 | CATATATATATATAT[-/TA]AAAGACCCTAGACTT | 57626 |
rs141019299 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765063 | TTCAAGTGATTCTCC[A/T]GCCTTAAACTCCTGA | 57626 |
rs141024967 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952294 | CCAAGTAGTATTTAC[A/G]TTTTTCAGGCATGGA | 57626 |
rs141048000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826648 | GGGAAAAATATTTGA[A/G]GCAATTTATATGTTA | 57626 |
rs141063507 | in-del | -/TTTC | 0.233527 | 0.249457 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723845 | CCAGTCAGAATTTTT[-/TTTC]TTTTTTTTTTTTTTC | 57626 |
rs141072365 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006917 | ACTCTTGCATATGTA[A/C]AAATTATTTTTCATT | 57626 |
rs141091126 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901886 | CAATGCAACCTCTGC[C/T]TCACGGGTTCAAGCG | 57626 |
rs141091937 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948452 | TTTGATCCTATAAAC[C/T]GCTTATAAAATTGGA | 57626 |
rs141102820 | snp | C/T | 1.71261e-05 | 0.00292622 | synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107223 | TCCACATCCTTCACC[C/T]GTTGCCTGGCTAGAG | 57626 |
rs141114149 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746966 | TGTCATTCAGAGACT[A/G]TAGCCAGCCCTAGCT | 57626 |
rs141139691 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753731 | CTACTTGAAGATTAT[A/T]CTCTACTGTATTCTA | 57626 |
rs141139704 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787258 | TACCTGACTTCAAAC[A/T]ATACTACAAGGCTAC | 57626 |
rs141149260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791642 | CCCTCACAGTTATGG[C/T]CAATTGATTTTTGAC | 57626 |
rs141153384 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864787 | TTAAGGAACTTACAA[C/T]ATATTAGGGCAAAAA | 57626 |
rs141189061 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994037 | AGAGTGTAGATTGGG[A/C]TTGAGAATGTACAAA | 57626 |
rs141189772 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936770 | GTCAGGGAAGTTTCT[A/C]CTGAAGATTTCAACC | 57626 |
rs141193434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850072 | CACATTCGATAGCAA[A/G]AATCCATTACAGAAA | 57626 |
rs141195669 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078405 | CCCCATTAGTTTTTT[A/T]ATGAGAAATTTAATC | 57626 |
rs141196347 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919921 | TTATCTTATGGCCCA[G/T]CTGTGTCCTTTCATG | 57626 |
rs141202244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003213 | CACATATTTTAAAGA[C/T]TGATAATCAAATCAT | 57626 |
rs141209264 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890699 | GTAAAGGCTAAGAAC[C/T]ACCATTCTTTAATCT | 57626 |
rs141222122 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969776 | TTTAGAAGAGGGATT[G/T]AATGCATAACAGACA | 57626 |
rs141223959 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743522 | GGACGTGGTGGCTCA[C/G]GCCAGTAATCCTGAC | 57626 |
rs141224170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807067 | TGGGCCGAGTTTTGC[A/C]TTTGGCCTGAGTTCA | 57626 |
rs141226123 | in-del | -/TTATTA | 0.305921 | 0.270806 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760347 | AAAGGTTAGGATATT[-/TTATTA]TTATTATTATTATTA | 57626 |
rs141238670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038106 | ACTAACTTGTTTTCC[A/T]TCTTCACGTTTAAGC | 57626 |
rs141244144 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953260 | TTGGGTATCATCTAT[A/G]TAACTTCCTCAGGCT | 57626 |
rs141263592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757426 | ATATTAATAATATAT[C/G]CATAAAAATTTAACT | 57626 |
rs141267479 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016909 | CTGAGCCCATAAAAA[A/C]CCCAGACTCAGCTGG | 57626 |
rs141273492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894736 | AATGATCTCCTTAGA[G/T]GACTTGATATTCATA | 57626 |
rs141275075 | snp | A/C/G | 0.000313624 | 0.0125187 | missense | KLHL1 | GRCh38.p7 | 13:69719490 | TCCTCTTACACATGG[A/C/G]AGCACACATGTTCCA | 57626 |
rs141281167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712174 | CTTTTTACCCTCTAA[A/T]TGGTATCTTCTGAAG | 57626 |
rs141293549 | in-del | -/TAGA | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825842 | AGTCTGAAGCCAAGT[-/TAGA]TAGAAATATTGCTGA | 57626 |
rs141296551 | snp | G/T | 1.64817e-05 | 0.00287064 | missense | KLHL1 | GRCh38.p7 | 13:69796944 | GTTCTCAGATCATAT[G/T]TCTCTATAGTTGTAG | 57626 |
rs141297470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077232 | TTCAAAGGTGAAATG[G/T]GTACAAAAGCAGTGG | 57626 |
rs141299753 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931956 | ATAAAATTAGGCACA[A/C]AAATATTTTAAATTA | 57626 |
rs141299854 | in-del | -/TTTTCAG | 0.0659589 | 0.169201 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087647 | AAAGTCCACTGTTTC[-/TTTTCAG]ATATCCTTTGAGCTG | 57626 |
rs141308102 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992299 | GACCTAAAGATAAAC[A/G]TATTACAATCTCTTT | 57626 |
rs141316188 | snp | C/G | 0.245631 | 0.249962 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033402 | TCACACCATTCTCCT[C/G]CCTCAGCCTCTCCAG | 57626 |
rs141325627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884035 | AGAAGCATTGTGACC[A/G]TGCTAAACAGAGTAG | 57626 |
rs141332783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854952 | AAATATATTTTTACA[A/G]GAAAAAAATTGTTGG | 57626 |
rs141347214 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813371 | GGAGATACACCTAAT[A/G]TAAATAACGAGTTAA | 57626 |
rs141353427 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706781 | AGGACACAAGTCAGA[A/G]TGTATCGATTCCCTC | 57626 |
rs141354266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780057 | GGGTGATCTACCCAC[C/T]TTGGCCTTCCAAAGT | 57626 |
rs141356515 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074167 | AAAAATTTTGATATT[C/T]AGCATGATTTGAAGA | 57626 |
rs141387279 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025751 | TTTTAAAAATATGTA[A/C]AGGCATATATATTTT | 57626 |
rs141388004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984291 | GCAGCCTTTAAAATC[A/G]AGCTGCAGACATAGA | 57626 |
rs141389911 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827716 | AGCCTGGCGACAGAG[C/T]GAGACCCTGTCTCAA | 57626 |
rs141399970 | snp | G/T | 0.0075629 | 0.0610735 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928282 | ACCTTGCAGTTTCCC[G/T]CCAATTGACAATCTC | 57626 |
rs141401054 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098097 | TTTTCTATCTAGTTT[A/C]ATTAACTCTGGTATT | 57626 |
rs141408447 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922955 | GAATAAATAATACAT[A/G]AAGATGAAATATTTG | 57626 |
rs141411712 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736833 | CAAACATAGTATATT[A/C]TCTCGTAAGTGGGAG | 57626 |
rs141412100 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765773 | TTGAAGCAACCACCC[A/C]GGCAATGCTACCCTC | 57626 |
rs141416113 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086674 | TATTTTGTTTTCTAG[A/C]TATTAATCACAGCTC | 57626 |
rs141419251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723785 | ACAACCCCTTATCAT[A/G]ACCCAGACATTCCTT | 57626 |
rs141424631 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990265 | CAACTACACAGGCAA[A/G]TCTGCATAATAACCA | 57626 |
rs141447437 | snp | A/G/T | 0.000210783 | 0.010264 | missense, synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107577 | AAAGCTGCCACTGCC[A/G/T]TCCTGTTGCAGGCAG | 57626 |
rs141461139 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69859375 | TGGGAATTATAAGCA[A/G]AAGGTCAGGGGGTGA | 57626 |
rs141465420 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810421 | CATGTATATTAAACA[A/G]CTTGCCCCTGAATGA | 57626 |
rs141469581 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879996 | TTCCATCTTCAGTGT[A/C]TTTAAAAGAACCTTC | 57626 |
rs141470670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100916 | GATTAAAATGCTGCC[C/T]GTTTTTATGCTCAGA | 57626 |
rs141478553 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989994 | TCAGCAGAAACCCTA[C/T]AAGCCAGAGGAGATT | 57626 |
rs141478799 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030017 | ATTACATAATGGTAA[A/G]GGGATCAATTCAACA | 57626 |
rs141479748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774461 | CAATTTGGCAAAATA[A/G]TGGAAATGACTTTTG | 57626 |
rs141484456 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025971 | TTGAAGGTTCAGGAA[A/G]GGCAGCAAAAGCCTT | 57626 |
rs141488761 | snp | C/G | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840443 | CGGCCAGGCTAGTCT[C/G]GAACTCCTGACCTCA | 57626 |
rs141488961 | in-del | -/TT | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822940 | TTTCAAAAATATAAC[-/TT]TATGTTTTTATAACA | 57626 |
rs141492945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881887 | TATGCATTTACATCA[A/G]TGGATGATCACATTA | 57626 |
rs141497514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769823 | TCCGGTATTCACGTA[C/T]CCTCATTCTTCTTGG | 57626 |
rs141503697 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861852 | TGCTTGTAATCCTAG[C/T]TACTCAGGAGTCTGA | 57626 |
rs141534115 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737295 | CTGGAGCAGGCACTG[C/G]ACACAGGAGTATTTG | 57626 |
rs141535312 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934019 | TTTATTATCCCATTC[C/T]AGCATGTCTATCTAT | 57626 |
rs141537684 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800040 | CAACCCCCACTCTCC[C/G]ACCCCTGTCCATGGA | 57626 |
rs141544559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777481 | ATATCTCTTGTACTG[C/T]AAAAGGATATTTTTC | 57626 |
rs141546495 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735441 | TAGTTTATTAAATGT[G/T]TATCTTTCTAGAAAA | 57626 |
rs141553562 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803482 | TGGGTAGAATTTAAA[A/C]AATTTCCCTTCCTGA | 57626 |
rs141566650 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913278 | CTCCAGCAAGCCCAA[A/G]TTTGGCTTCCCAGGA | 57626 |
rs141583070 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966382 | ACTATAAAGCCTGGA[C/T]GACAGCACATCGTTT | 57626 |
rs141587533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982126 | CTTATAGTAACTAAA[A/G]AGCAAAAACCTATTA | 57626 |
rs141597455 | in-del | -/TTC/TTCT/TTTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69723846 | CAGTCAGAATTTTTT[-/TTC/TTCT/TTTC]TTTTTTTTTTTTCTG | 57626 |
rs141598033 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801787 | AAGAGATAGGTGTGT[A/G]GCATTTGTAGTAATA | 57626 |
rs141600105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872867 | CAGCCATTCATGAGG[A/G]ATCCTCCCCAATGAC | 57626 |
rs141620103 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873392 | CTATTCTCTCTCTCT[C/T]AAATTAGGTATTAGA | 57626 |
rs141626060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738959 | TAATCATCAGATTCG[C/T]CAAAGTCGAAATGAA | 57626 |
rs141629234 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906129 | TTCCTTCTCAATACC[A/G]CATGAGAACTATTCA | 57626 |
rs141630224 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048745 | TGATGCCAGCGATGG[A/C]GAGCAGTTGTAAATA | 57626 |
rs141631329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949723 | ATTGGTGTATTCAAT[C/T]ATTTATATCAGTCAT | 57626 |
rs141632976 | in-del | -/ACA | 0.435487 | 0.167614 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067634 | AGATGACATATTTTG[-/ACA]ACAACAACAACAACA | 57626 |
rs141647147 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948745 | TTTCTTATTAGACAC[A/T]TCATCCCCTATTAAC | 57626 |
rs141656154 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69974788 | TCAGGATAATTTGTG[C/G]TTTTGCCACACATAT | 57626 |
rs141661386 | in-del | -/TGTC | 0.400504 | 0.199621 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789270 | TTAAATTATTTTACA[-/TGTC]TGTCTGTCTGTCTTT | 57626 |
rs141674256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882072 | CATAATCTTACAAGT[A/G]GCCATGAGTCAATAA | 57626 |
rs141677615 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951029 | TAATATATCAACACC[C/T]GTGTTTATGGTGAGG | 57626 |
rs141677645 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041012 | TTCGTTTGACATCTC[C/T]ACTTTGTTAATGAGT | 57626 |
rs141684139 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842845 | ATACACAATAGAATG[C/T]TACTTGGCCATAAGA | 57626 |
rs141688753 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942246 | AATGGCAGCCTTTAG[G/T]GCCTACATATAAGGA | 57626 |
rs141689373 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69877343 | AAATCAGTGGAAATA[A/C]TTGTTATAAAATGTT | 57626 |
rs141694184 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69911321 | CAATTGTTGAAAAAG[C/T]ATCAAACTCACTTTT | 57626 |
rs141700182 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778483 | TTCTTAACATCATTG[A/C]CGAATATAGTATCTT | 57626 |
rs141706605 | in-del | -/AT | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755836 | TAAATAAAATGAAAC[-/AT]GTGGGTAGTGGAAAA | 57626 |
rs141706864 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844853 | TTCATATGTACAAAA[G/T]AAATTTCTGTTTTCT | 57626 |
rs141711208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086264 | GCCCCAGAAATGAAG[A/G]GTTAAATAAAAAGTT | 57626 |
rs141718193 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947365 | ATTTCTTTATATGTG[C/T]GTGTATTTTTACTTC | 57626 |
rs141737239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722981 | TGGAACACAATGGAA[C/T]ACTATTCAGCCATAA | 57626 |
rs141737950 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080831 | ATTTGAACCTCCTGA[C/T]CTCAAGCAATCCTCC | 57626 |
rs141746093 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984954 | TCTCTACTAAAAAAA[C/T]AGAAAAATTAGCCAG | 57626 |
rs141754940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044227 | CTACATTTGCTCCCA[C/T]GTACATGCACTTCAC | 57626 |
rs141774602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005682 | TGTATTGCTTATTTC[A/G]CTTTGATTAAAATAT | 57626 |
rs141776888 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69815294 | AATAGCAAAGACATG[C/G]AATCAACCCAGTTGC | 57626 |
rs141778406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838715 | CAACAAATTGTTTGG[C/T]TTGTGTTAAGTGATT | 57626 |
rs141780250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887190 | ATATGCATGGTTCTA[C/T]TATTTTAAGGATTGA | 57626 |
rs141810483 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782196 | GGGAGTCAAGATGGC[C/T]GAACAGGAACAGCTC | 57626 |
rs141816654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791777 | AAATAACTCAAAGCA[C/T]GGATCATATTTCTTA | 57626 |
rs141820558 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865224 | TTGCAGGCCTGAGCC[A/C]GTGCACTCGGCCCTG | 57626 |
rs141822817 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892129 | TGATAAATTGCTGAA[C/T]ATCGGTATTTGCCAA | 57626 |
rs141830284 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756387 | TTTCTGATCAATATT[G/T]TATTGATTCTTTAAA | 57626 |
rs141831413 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081369 | ACTTAGGGAATTACA[C/G]TGCTGCAATCAAGAT | 57626 |
rs141849776 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761439 | GGTATGATGGAACTT[C/T]AGGCTAAACTTGATG | 57626 |
rs141849820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783302 | TGCAGCTCCTCACCA[A/G]CAATAGAACAAAGCT | 57626 |
rs141854645 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957727 | TACCAATTATAAAAC[A/G]GCACTACTTTATAAC | 57626 |
rs141855195 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043353 | TAAGGAGTCAAAATG[C/T]TAAAAGTTTATAAGT | 57626 |
rs141897462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001355 | ATGTTATATGAATTA[C/T]CCTCATTAAAGAAAA | 57626 |
rs141897565 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046612 | CGTGCTTCAGCTTCC[C/T]TAGTAGCTGGGATTA | 57626 |
rs141906402 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062244 | TGAGCTCATGAGAAA[G/T]TTTGAGATAAATATG | 57626 |
rs141914108 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818284 | GGAGTGCAGTGGCAC[G/T]ATCTCAGCTCACTGC | 57626 |
rs141915092 | in-del | -/AAT | 0.225597 | 0.248806 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868019 | AAAAACAAAAAACAA[-/AAT]AATAAGTTTTGATAA | 57626 |
rs141918818 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857986 | AAACATGCTATGTAT[C/T]CTGAATTTAAACAAT | 57626 |
rs141919929 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797591 | GGAGGCCGAGACGGG[C/T]GGATCACAAGGTCAG | 57626 |
rs141924499 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895442 | GCACATTTAACAGAG[C/T]CATTAAATAACTTTG | 57626 |
rs141925259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095487 | TGGCAGTGAGACTGG[A/G]CCAATTGCTTGCCCA | 57626 |
rs141926425 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826431 | GTCCACTAAAAACAC[A/T]AAAAAACCCATAGTG | 57626 |
rs141929738 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896304 | CTGCTTTTGCAGACT[C/G]ATGCCGCTACACTTG | 57626 |
rs141944006 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734662 | AATACTAACAGAGAA[A/G]AATAACAAATTAGGA | 57626 |
rs141948898 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69756646 | AAATTAACATGGTAA[A/C]TTAAGTAACTAAATT | 57626 |
rs141959578 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759541 | TAGAAATATTACATA[C/T]ACATAACATAAAGAC | 57626 |
rs141963407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715268 | TGCTGAGGGAGAAAC[C/T]TGGTGGGGGGTGATT | 57626 |
rs141970950 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754727 | TTTAACATTCTCTCT[A/G]TTGCACAATGGCTTT | 57626 |
rs141973704 | in-del | -/ACAC/ACACAC/ACACACAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69813481 | TATATACACACACAT[-/ACAC/ACACAC/ACACACAC]ACACACACACACACA | 57626 |
rs141977026 | in-del | -/A/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69808537 | TCATATCCCCAAGGT[-/A/AA]TAAAAAAAACAGAAT | 57626 |
rs142001754 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104938 | TAAAATATTATATAC[C/T]GATAATGATTAATTG | 57626 |
rs142006094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034687 | GAAGAGGTGCATGTG[C/T]ATTTTGAGGAAGAGG | 57626 |
rs142009162 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69907212 | AATTTTTAAAAACTA[C/T]TTGACCTTTAGGCGT | 57626 |
rs142013340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937314 | AATGAGAAACACTTA[A/G]AGACCACTGCTTTAA | 57626 |
rs142030539 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839817 | TTTTTGCTATAATAG[G/T]TTATTGTCTCTGCAA | 57626 |
rs142031012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893002 | ACTAGTTGCTTACAA[C/T]CAACATTTAAAAATC | 57626 |
rs142033056 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067866 | CCAGTGGAGCAAAAT[G/T]TTACCCAAACATAGA | 57626 |
rs142039036 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957806 | AAACAGTGAAGAAAA[C/T]CCAATTGAAAGTCTT | 57626 |
rs142041253 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895965 | CACTCACCTCTGCCT[C/T]CCAAAGTGCTGGGAT | 57626 |
rs142044717 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064627 | TTCACAGGGTAAGAG[A/G]CTATTGCCTACCGTT | 57626 |
rs142044962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866088 | TGATTAAATATTCAT[C/T]ACTCCCTAAATTCTC | 57626 |
rs142046551 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927616 | AGCAACATTTCTCCA[A/C]AGAGGATATATAAAT | 57626 |
rs142046561 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964848 | CTTTAAACAACTGGG[A/T]CATCTCTTGGTCAAT | 57626 |
rs142051514 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961866 | AATAAAATAGTATTT[A/T]TAAATTAGAAATATG | 57626 |
rs142072544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763898 | AAGTCTCCTCTGTTG[C/T]AACCCTTACAAAAAA | 57626 |
rs142081460 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958260 | AATAATAATAATAAT[A/T]ATGTAAGTCTACATG | 57626 |
rs142106747 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859817 | TATGTCAGTAGAATG[C/T]GTTTTGCATAGGCAA | 57626 |
rs142112795 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931748 | AAAATATTGAACACA[G/T]ACACTGAGTAGAAAA | 57626 |
rs142117483 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902870 | TGCAACTAACCTGCA[C/T]GTTGTGCACATGTAC | 57626 |
rs142121050 | in-del | -/TAATA | 0.0352966 | 0.128072 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953139 | GATTCTTCTTCAGAT[-/TAATA]TAATAAAATAAAATT | 57626 |
rs142139376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959306 | TGTTAGGTTGTTAGA[A/T]CTCTGTCTTTTAGTT | 57626 |
rs142140914 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736411 | TTTGGCATGGATGTG[G/T]TGAAAAGGGAACACC | 57626 |
rs142149199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799355 | GAAATTAAGACTTCC[A/G]AGCAAGCAAAGGAGT | 57626 |
rs142150938 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69836855 | TGCTCAAGAAACTGC[-/AA]AAAAAAAATGCAATA | 57626 |
rs142152542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063404 | TTTTAACATTTAGTA[A/G]AACTTCATTGGCACC | 57626 |
rs142158962 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993629 | TGACTGTGAATTCCA[A/G]GTATATTATTTCTTC | 57626 |
rs142187908 | snp | C/G | 0.031825 | 0.122064 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964854 | ACAACTGGGTCATCT[C/G]TTGGTCAATTTCCAT | 57626 |
rs142190636 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025497 | TAGACAAGAACATGC[A/G]TGAAATATCTAACTT | 57626 |
rs142190733 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857275 | CTCTTCCAAGACACA[A/T]CATATGTCACCTCCT | 57626 |
rs142202260 | in-del | -/CTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69709659 | CATTAAAAAATAAAG[-/CTT]TCATTATTTTTGTTT | 57626 |
rs142208406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106808 | CAGTTACTAGGCCAA[C/T]ATATGAGATGCATTC | 57626 |
rs142216506 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008883 | CTTGTAATAGAAAGC[A/T]ACCTCAAAAATGGAT | 57626 |
rs142219449 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949410 | TTTGCTGATTATTAG[A/G]CTGGGGTTATGAATG | 57626 |
rs142221429 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841860 | AGGCCAATGGAACAG[A/G]ATAGAGAGGCCAGAA | 57626 |
rs142225654 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69910036 | CATATTCCACTTCGC[A/T]ATCATCATCTATAAA | 57626 |
rs142228460 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099246 | ATAAGTAAAAATTCA[C/T]TCATTCTCTTCCCTC | 57626 |
rs142238090 | in-del | -/T | 0.183886 | 0.241099 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705218 | GAAGCACGTGCATTA[-/T]TTTTTTCAAATCAAA | 57626 |
rs142269123 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061764 | CACAGTTTCTCTTTT[C/T]TTGTGTGTTTATTTA | 57626 |
rs142274161 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738002 | GCTGGCATCAGGTTG[C/G]TGCCCCTCTGAGACA | 57626 |
rs142296626 | in-del | -/TTTA | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951227 | CCTTTCCCAGTATTT[-/TTTA]TTTGACTTACAAAGC | 57626 |
rs142305899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065434 | TTAGGGAAAGCACAA[C/T]AGAGTGGGGAGATAT | 57626 |
rs142316249 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837705 | ACATATATATATAGA[C/T]CTCATATTTTTTGAA | 57626 |
rs142319175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872937 | ATTAAATTTCAACAT[A/G]AGGTTTGAGGGATGA | 57626 |
rs142332299 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005034 | TAGTTTTGTAGGATT[G/T]TATGTTTTTAGAATA | 57626 |
rs142337047 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771972 | AATTGTTATTTTTGA[A/G]ATGGAGTCTCACTCT | 57626 |
rs142342859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922233 | ATTACTTGTGTGAAC[C/T]GTCACACTGGCCTAG | 57626 |
rs142343108 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733615 | TATTAAAGATGTTTG[A/G]TCACATCAGTTCTTA | 57626 |
rs142347563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775313 | CTAGTGACTCAAATG[G/T]CTAAACATTTGAATA | 57626 |
rs142349042 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809577 | TAGACATGGAAATGA[A/C]AGGATTATACTTGCT | 57626 |
rs142349296 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842312 | AAGAGAGGACAAATA[C/T]GCAGAATGTACAGGA | 57626 |
rs142369811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718052 | CCAATGGACTTATCA[A/G]TAAAAATAATTACTC | 57626 |
rs142376747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806599 | CCTGGACGTGGGGAA[A/G]CAATAAGATAGAAAC | 57626 |
rs142377988 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69964034 | GCACCACTGTTGGAA[-/T]TTTTTTGTCAGTTTG | 57626 |
rs142378365 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770164 | TCTGAGTTTTTAGGC[A/C]CCACTGCATTCCCCT | 57626 |
rs142388313 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060499 | ATTTACAATAGCCAA[A/C]ATTTGGAAGGAAAAC | 57626 |
rs142394859 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980455 | TGATGCTTTCTACAA[A/T]TTGTGTGATCCTTCA | 57626 |
rs142407863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019124 | AGATCATTCTTTCAA[A/G]GCTCTTAAACCGTAA | 57626 |
rs142416836 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758737 | AAAGCTATTTCCTCA[A/G]TTTTTTTGTTTACTG | 57626 |
rs142437506 | in-del | -/TA | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842824 | ATAAAGAAAATGTGG[-/TA]TATATATACACAATA | 57626 |
rs142448807 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909434 | CTAAAACTGCAAATA[C/T]TTGAAGCAAAGAAAA | 57626 |
rs142453738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855673 | AAAGAAGGTCCCTGC[C/T]TCCCCTTCCCCTTCC | 57626 |
rs142455222 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011273 | TTAAATGCTTTGGAA[C/G]TATCCATTAATTCAA | 57626 |
rs142459531 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914135 | CTGCTCCTCAGCTTG[C/T]AGACGGCCTATTGTG | 57626 |
rs142474478 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69876434 | CTTTTGGAATAATTT[A/T]TTCAGCTTTACACAG | 57626 |
rs142474715 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832455 | AAGAAATCATTGATG[A/T]CAGAAACAAATGGAA | 57626 |
rs142475028 | in-del | -/G | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933521 | AACCACATTGATATA[-/G]TTTGTTCTTTCTATA | 57626 |
rs142481988 | in-del | -/TTGTC | 0.0441095 | 0.141807 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917880 | AGTTTGCTGATAGCT[-/TTGTC]TTTTCAGTTTTTCAC | 57626 |
rs142484994 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946258 | ATATATTCATTACTT[C/T]GTGGTGAGTATATAC | 57626 |
rs142493660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829439 | CAAAATAATCTGAAC[A/G]CAGCCCTTAAGCCCC | 57626 |
rs142495980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978421 | TTAAATAGGGTTTGG[A/G]ATAAAAGCTCTACAT | 57626 |
rs142514838 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977296 | AAAATAACTTTCATT[C/G]GTCTTTTAATATAGA | 57626 |
rs142523697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724610 | AAAAATTATCATCAT[A/C]ATACCTGCAAACTGA | 57626 |
rs142527920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931286 | AAGATTTACTATTGG[C/T]GAAATAGTTCATTTT | 57626 |
rs142533570 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089335 | GTTATTGTTTTTAAT[G/T]TGTCACTAGAAGATC | 57626 |
rs142553856 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043125 | AGCCAGGCTGATCTC[C/G]AACTCCCGACCTCTG | 57626 |
rs142565741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870805 | AAAATCATCTCCTGT[A/G]ACTCTATGTCCGGCA | 57626 |
rs142576245 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008212 | ATCAGGTTGTCATAA[A/C/T]AGTATTTATAGGTTT | 57626 |
rs142593487 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771135 | GATAAGTCTTCAAAT[C/G]AAGACTTTTCCAACT | 57626 |
rs142599594 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032850 | CTTTTTAAGGTTACT[A/G]TGTGGTTGGTGCAAA | 57626 |
rs142604240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718530 | ATTTGTTAGAGTAGA[A/G]TTACTTATACCAATT | 57626 |
rs142605018 | in-del | -/AAAT | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977360 | AAATCAAATGGAAAC[-/AAAT]AAGGCAATACAATAA | 57626 |
rs142634597 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080199 | TCTGCTAGTCTGAGT[A/G]CTATCTGATTGGACC | 57626 |
rs142636003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936135 | AGGGAGAGATTATTC[A/G]GAATTTGATAATGGA | 57626 |
rs142641918 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860971 | GTTTATAAAAATAAT[A/C]AATTAATTATACCTC | 57626 |
rs142651778 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69750379 | TAGAATTGAACACTT[-/C]AGTGTTTTTCTGTGC | 57626 |
rs142653645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045018 | AACACCTAACTCTCA[C/T]GGGTGCTATGTATAA | 57626 |
rs142668332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075945 | AAAATGCATACAAGA[G/T]CTATATGAGAAAAGC | 57626 |
rs142686574 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915321 | CAAAGCTGGAGGCAT[C/G]AGGCTACCTGACTTC | 57626 |
rs142688784 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979836 | AAAATGAATAAAATT[A/G]TTTTGATCTCTTGAA | 57626 |
rs142689871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70049361 | TCCTTTTAAAATTTT[A/G]CTACCCACATTTAAA | 57626 |
rs142699312 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757744 | ATCACCTGAGGTCAG[A/G]AGTTTAAGACCAGCC | 57626 |
rs142700365 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874846 | AGCTTTGGGGTAAAT[G/T]ATGTAGGGCTTTGTA | 57626 |
rs142714505 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967628 | CGTTGTGGCTCACGC[C/T]TGAAATCTAAACTTT | 57626 |
rs142717192 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758248 | GATAAACCAATTTTT[A/C]CTTTTATATTAGTGT | 57626 |
rs142725535 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820287 | CAGGGTTCACATATC[A/G]GTTATCATAACGTAT | 57626 |
rs142745982 | in-del | -/AAT | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791239 | GATAATAATATCAAA[-/AAT]AATAAATTATTTAGG | 57626 |
rs142755438 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740692 | TAAAAATTGAATAGA[C/T]TTATTTCACAGTGAG | 57626 |
rs142763899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999500 | CAGACCTAATTTCAA[G/T]TATAAACTTTCCCTT | 57626 |
rs142774363 | in-del | -/TCTGTGTG | 0.0599851 | 0.162463 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042268 | TCATTTCTTTACATA[-/TCTGTGTG]TCTGTGTGTCTGTGT | 57626 |
rs142781948 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717800 | CACATTTGTGAGTAT[A/C]AAAGCATAAACCTAT | 57626 |
rs142787978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823761 | CCACTTCTCTTACCT[C/T]TTGCTTGCTTACTCC | 57626 |
rs142807932 | in-del | -/CAAA | 0.0577344 | 0.159793 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059086 | CAAATACTAAAACCT[-/CAAA]CAATGAAACTACTAC | 57626 |
rs142809901 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709798 | ACAATAAGAACAAAT[C/T]TGTGATCGTTGTTGA | 57626 |
rs142817329 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781994 | CAATTGCAGCAAACA[C/T]TTTAAATTTGAAGAG | 57626 |
rs142843119 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985745 | CCTAAGTGTTCATCA[A/G]AGGCTAAATGGATAA | 57626 |
rs142845627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929055 | ACTTAATGACAAGAC[A/G]GCACTTATCAACATT | 57626 |
rs142846510 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965573 | GTCCAAATGAATGGA[A/C]GTGTTGCATGTCTCT | 57626 |
rs142862185 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042881 | TGGAGATATGGAGGG[G/T]GAAGACAGTGATATT | 57626 |
rs142866146 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883924 | AGCAAAGGCTTCTCA[C/G]GTTCTAGTTTTAAAG | 57626 |
rs142873321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847828 | ATGACAGTTTCATAG[C/T]TTGCCTTTCAAGTTT | 57626 |
rs142876799 | in-del | -/T | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69970007 | CCTTTTTTAAATCTA[-/T]TTTTTAGCGAAAGCT | 57626 |
rs142881771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923756 | GCTGCAGTGGAGGAG[A/G]TGCAGCCAGGGCTAC | 57626 |
rs142883419 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110457 | TTATATTATTTTCAC[G/T]TGATTGTTACCATAC | 57626 |
rs142894988 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882117 | ATTTAGATCCACGAT[C/T]CATCATCATACATCA | 57626 |
rs142895354 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927896 | AGGCACATACACCCC[A/C]AAATGAAAATATTAT | 57626 |
rs142899951 | snp | A/C | 1.66796e-05 | 0.00288782 | missense | KLHL1 | GRCh38.p7 | 13:69940087 | CAATGCATCCTTGAG[A/C]ATCTGCGAAGGCTCG | 57626 |
rs142903605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861555 | GCATATATATGCATA[C/T]GTATATATATACACA | 57626 |
rs142930393 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068728 | ATAAATTCATGTAAA[C/T]AATTTAATAGATTAT | 57626 |
rs142931044 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720977 | CCTGGGACTCCCAAA[C/T]CACTAAAGCCAAAGG | 57626 |
rs142941856 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812036 | CTTTCTCTTGTGGGC[A/G]TTTAGTGCTATAAAT | 57626 |
rs142966357 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70028486 | ATTAAAAGAGACCCA[C/T]GGCAATTCAAAATGT | 57626 |
rs142966710 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817619 | AGGGAGACTATTTCT[A/C]TTTTCCAGAGAATAG | 57626 |
rs142971193 | in-del | -/AAT | 0.264358 | 0.249587 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987005 | TTTTTTTAGATCATG[-/AAT]AACAAGATAAAATAT | 57626 |
rs142971322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054493 | ATCCATTCTATTGTT[A/C]ATGGATATTTGTTTC | 57626 |
rs142985707 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086602 | AAAAAAAGAAAGAAA[A/G]AAAGAAAGAAAGAAA | 57626 |
rs143003987 | in-del | -/AG | 0.0584853 | 0.160693 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058101 | AATATGCCTCAACAC[-/AG]AGCCATATATGACAG | 57626 |
rs143012689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060160 | AATGGAAACAGGTGT[A/G]TGAAAAGGTGCTTAA | 57626 |
rs143040790 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877077 | CAATTCTGAGCTAGG[A/T]AGCAAAGTTTATATC | 57626 |
rs143044838 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063898 | TGTTTATATGATTGG[A/G]TGCTTTCTTTTTCTT | 57626 |
rs143051296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053109 | GAAAAATGAAAAAGC[A/G]ATGTGTAAATGGTGA | 57626 |
rs143058757 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953058 | GTTGAATACTGTGAG[A/G]CATAGCTAAGATTTG | 57626 |
rs143070009 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787648 | TGGCAACTAAAGCCA[A/G]AATTGACAAATGGGA | 57626 |
rs143077031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859947 | CAACAGAAAAACTCA[A/G]TCTATCATCTGAAGG | 57626 |
rs143080354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781753 | ATTGCTTTCTAGGAG[A/G]ATCATTTTAGAAGCT | 57626 |
rs143086206 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849682 | CCATATATGTAGTCA[C/T]TTAAAGGCTTAAAAA | 57626 |
rs143091524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044169 | TACTTCTCACAGCCC[A/T]GTTCATACTGGCCTT | 57626 |
rs143099834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773533 | TGGTAATAAGAGAAC[A/G]TGTAGAATTGCTAAT | 57626 |
rs143102592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757244 | ACTTACAGAAATGCA[C/T]AAGAATATGAACAAG | 57626 |
rs143107734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097034 | GTAAAGGAGGTTATT[G/T]GAGGAAAAATACTTA | 57626 |
rs143112784 | snp | A/C | 0.000165096 | 0.00908408 | missense | KLHL1 | GRCh38.p7 | 13:69740531 | GCCTCCCACAGCATA[A/C]ATAGGGCCTTCAAGT | 57626 |
rs143120658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092381 | TACTCCATTTAGAAC[A/G]TTTGATTCACTACTC | 57626 |
rs143130560 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021632 | GTATTCCCATCAGCA[A/C]TGAATGAGAATTCTT | 57626 |
rs143132268 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989467 | TGGTTCCATATGAAT[C/T]TGAGAATTAGTTTTT | 57626 |
rs143141328 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038157 | TAAATTTAATATACA[-/G]TAAAGTGACCTTTGA | 57626 |
rs143142986 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734025 | ACAGAGTTTGGATGT[C/G]TGTCTCCACCCAAAT | 57626 |
rs143143197 | snp | A/G | 0.00266908 | 0.0364337 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69796751 | ACCTAGACCATGTCT[A/G]TGTGTTGACATTGGT | 57626 |
rs143148694 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69897670 | TGTCAGAGGACATGA[A/G]CACCTGATACCCTCA | 57626 |
rs143160366 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69891254 | ATTAATTCTATAGCA[A/C]CCACTAAGTGGTAGC | 57626 |
rs143160500 | in-del | -/TTG | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081897 | AGTTGGTCACTGATA[-/TTG]TTTGGATTTATGTCC | 57626 |
rs143166959 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833137 | AATAAGTTTCTGCAC[A/C]CCAAAGGAAATAATC | 57626 |
rs143169519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024726 | GGAACAATTATGAAC[A/G]GAAGTTGGAGAGAAG | 57626 |
rs143181208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791663 | GATTTTTGACAAGGG[C/T]GCCAAGAATTCAGTG | 57626 |
rs143216168 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067124 | CAAACCTGTTATTAC[A/G]TGATCATCCAGTTAC | 57626 |
rs143224134 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972272 | GTCACTTTAGCCTCA[A/G]CTGTCTACATACTAG | 57626 |
rs143224324 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69796274 | GTCATAGTTTGGATG[C/T]TTGTCCCCCCAAAAC | 57626 |
rs143238827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792493 | GGAAAACAGTTTTGC[A/T]GTTTCTCCAAAAGTG | 57626 |
rs143250126 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767186 | GATATATTAGCGTGA[A/C]TTTTTGTTTCAGGCC | 57626 |
rs143252634 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867932 | GGGTGCAGCACACCA[A/G]CATGAAACATGTATA | 57626 |
rs143254452 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829800 | GGTCTTATCTTTAGC[C/T]TCCTTAAACAAAACA | 57626 |
rs143261080 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025754 | TAAAAATATGTACAG[A/G]CATATATATTTTTAT | 57626 |
rs143262084 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961232 | TTTTTTTAAAAAAGC[A/G]TTAAATCCTGTACTT | 57626 |
rs143298983 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905494 | ATGAATTAAATTATT[C/G]ATCAACTCCATGATA | 57626 |
rs143308789 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941519 | GTCCGAAAGAGCACA[A/T]ATAGAGAATCTAGGG | 57626 |
rs143315520 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770410 | ACCAAAACTATCCTA[C/T]GTCATTGACAAGCTG | 57626 |
rs143318239 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074290 | CTCTCGGCATCACTA[A/C]AGTTGCCACTCCTTT | 57626 |
rs143319896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836599 | TGTTTGGAAGAAGGC[A/T]ATTTTCTGTTACTCT | 57626 |
rs143321594 | snp | A/C | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997092 | TGGATGTGGTGGCGC[A/C]TGTCTGTAGTTCCAG | 57626 |
rs143322133 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706906 | AACACACATCCTCTA[A/G]TTATGTGATTACAAT | 57626 |
rs143322981 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899244 | TCTAATGGGGTGAGG[A/G]CAAGCAAATCCAGGT | 57626 |
rs143326546 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801229 | ACTGAAAAATAACAA[A/T]CACTACTTTGTTGTT | 57626 |
rs143343158 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69744487 | ATGTTTCAAAGTATA[-/AT]ATATATATATTACAT | 57626 |
rs143344746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041511 | TGTTACTGTTGGGTA[A/G]GGGTAAAGTGGGAGT | 57626 |
rs143348887 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871023 | TCCACAGGGAAGTGT[C/T]CTAGCAGTTATTCTT | 57626 |
rs143362104 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828922 | CCAAGGAGAGTCTGA[A/G]CTCAGATATGCCTAA | 57626 |
rs143372760 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950389 | ACTCACATCGATGCA[C/G]AGGTGTTAAGCTCCC | 57626 |
rs143393971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813394 | CGAGTTAATGGGTAC[A/G]GCACACCAACATGAC | 57626 |
rs143398796 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843526 | GTGGATTAATTTTAG[C/T]TTACAAGTAACCCTA | 57626 |
rs143405041 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912710 | TTAGGCCAAGTCACC[A/G]CCAGACTCTGCCCCT | 57626 |
rs143408184 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708930 | CATAGACTCCTAAAA[C/T]AAATGAAGAAATAAA | 57626 |
rs143412796 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942635 | CACCCATATAACCTT[C/T]ATCTGGCTTCACCCA | 57626 |
rs143418216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752803 | ACTCAGGCTATATAT[A/G]GCCATAAGCGAATAG | 57626 |
rs143419445 | in-del | -/T | 0.143959 | 0.226396 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713707 | TTTGAAATGAGAATA[-/T]TTTTTTTTCATATTT | 57626 |
rs143427999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078037 | CTGTTCTCTACAGGT[A/G]CCTCTCTAAATGATC | 57626 |
rs143436165 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001876 | CATTATATCTAATTA[A/T]GGCTTAACATCTAAT | 57626 |
rs143468065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037343 | TCATTCTATAAGCAC[A/G]TTGAACATATAATTT | 57626 |
rs143474509 | in-del | -/AATAT | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953625 | TATGATAAAATCATG[-/AATAT]AATATACAATAAAAA | 57626 |
rs143476000 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923524 | TGCTTTTATTTATAC[G/T]TATTATTTTTAAAGT | 57626 |
rs143490225 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984749 | GTTCTTGATTTCCTC[A/G]GCATGAGGCAAGGGA | 57626 |
rs143491732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822947 | AATATAACTTTATGT[A/T]TTTATAACAACTTAT | 57626 |
rs143495964 | in-del | -/AGAGTC | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003306 | AAGGGAAAATGTAAA[-/AGAGTC]AGAGAAAAGTGGATA | 57626 |
rs143498075 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867686 | TAGTAAAAGAGAGGG[C/T]TTGTAAGTATATTAA | 57626 |
rs143501835 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69811033 | TCACAGCAGAATTCT[A/G]TCAGACATACAAAGA | 57626 |
rs143503437 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939653 | TAAGTGTGCATAAAG[C/T]CATAAAGAAGCTTCC | 57626 |
rs143506136 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108824 | CCTTAGTTTCTCTGT[A/G]GTGAGACACAGAAGA | 57626 |
rs143506649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080606 | TACTTTGTTTTATTT[C/T]ATCATTTTTGAGAGG | 57626 |
rs143508966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882012 | ATGGCAGTATGATCA[C/T]ATTTTATAAAGAGAT | 57626 |
rs143514542 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975351 | CTCCATAGTTATCAA[A/C]CCTAGTTACAAGTAG | 57626 |
rs143518222 | snp | C/T | 8.25634e-05 | 0.00642455 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69719506 | AGCACACATGTTCCA[C/T]TTATTTGTATGAGGA | 57626 |
rs143550686 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038133 | AAGCCATTTCAAGAA[C/T]GCTATGTATAAATTT | 57626 |
rs143554043 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701585 | ACATCAGTAGGTAAC[A/G]CTACAGAGATCCTTG | 57626 |
rs143555811 | snp | A/T | 0.0136125 | 0.0813693 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997682 | TATATATAATATTAC[A/T]TATATATATAATATA | 57626 |
rs143557827 | in-del | -/AG | 0.108402 | 0.206034 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088668 | AGCCTGGGGTAACAG[-/AG]CAAGACCCTGTCTCA | 57626 |
rs143582665 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927946 | TATGAATGTTCATAG[A/C]AGTCAAGCTATCCTC | 57626 |
rs143587917 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854468 | AGGGATCCTCTACCA[C/T]GACCCAAACACATCC | 57626 |
rs143591373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042146 | AATGTAGTTTGGGAT[A/G]TATAAGGAAAAAAAT | 57626 |
rs143595428 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765549 | TTAATTCCTACAATG[A/T]CCGTGTCACAATGTC | 57626 |
rs143597558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923564 | AATTAAAATGATTAT[C/T]ATTACTACTATGTTA | 57626 |
rs143629871 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101492 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTTACTGT | 57626 |
rs143633527 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109415 | CACAGTTTCAGTAAC[C/T]CCCAACAGAGCATAG | 57626 |
rs143647021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748169 | AGTGAGACTATCAGA[A/G]GTGGCGACAGAGCAA | 57626 |
rs143671208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832117 | AATCGGACAAAAGAA[A/G]GAAATAAAGGGCACC | 57626 |
rs143675520 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901900 | CCTCACGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 57626 |
rs143682399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993069 | TAACACTATTTATTT[A/G]CCTATATATACATAT | 57626 |
rs143685216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852264 | AGGTAATGGCCTCAC[A/G]TCTGTAAAAAGCATC | 57626 |
rs143687910 | in-del | -/TTTC | 0.164219 | 0.234823 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024679 | CTGGCTCTGTCTCTT[-/TTTC]TTTCTTTATTTCTCT | 57626 |
rs143702595 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734105 | TAATTGGGTCATGGG[A/G]GCAGATTTCTCATGA | 57626 |
rs143721701 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944446 | ATGTATTATTTTGCC[A/G]TAACAATTCATAGCC | 57626 |
rs143725008 | snp | G/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953962 | TAATTTTATAAGTTT[G/T]CTCCTTAAAATAACC | 57626 |
rs143726949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017468 | ACCTGGAGCTGCCCA[C/T]TCTGCTGCAGCAACT | 57626 |
rs143737673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920372 | ATCCATTTGTGGTTC[A/G]CAGTGCTATTTTAAG | 57626 |
rs143737714 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957593 | GACCCTCTTCATGCC[A/G]TAAGTGCTCAAATAT | 57626 |
rs143738763 | snp | A/C/T | 0.121611 | 0.218679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783551 | cctcaggagccgatg[A/C/T]gatcaactggaagaa | 57626 |
rs143738983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746392 | ATTTCCTTTTATTTA[A/G]TAATGCTTACTGCTC | 57626 |
rs143742227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034227 | TTATTATTGCTATCT[C/T]ATTGAACTTCCCCAA | 57626 |
rs143743002 | in-del | -/T | 0.368938 | 0.219895 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757789 | GTGAAATCTCGTCCC[-/T]CTACTAAAAATGCAA | 57626 |
rs143745009 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052454 | AACTACAAGAAAATT[-/A]AAAAAAAACCCTTAT | 57626 |
rs143746239 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969117 | TATCTTACATATAAG[A/G]TAAGTGGAAGGACAT | 57626 |
rs143748728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772992 | AGCAAGAATAATTTC[A/G]GGAAGATCCGAGTGA | 57626 |
rs143780669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838918 | CACCATTACAATATA[A/G]AAGCTGCAACACGGT | 57626 |
rs143781379 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850852 | GTCAAGGCTGTTCTA[C/T]ACATTATCCTTCACG | 57626 |
rs143800179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091064 | GTTTTATTCCCGTGC[G/T]TATGACTCTCAACCT | 57626 |
rs143807759 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046854 | AAGTACCGAAGCTGC[A/C]ATCAGGACCCTCTTC | 57626 |
rs143812283 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980899 | AATATATTCTATGAC[A/T]AGATGGTTTGGTCAG | 57626 |
rs143824100 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728631 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 57626 |
rs143826420 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888726 | TGCAAAAAAGTAAAT[A/G]TAATGTCTTTTAAGC | 57626 |
rs143828895 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077851 | TTATCCAATAAAATC[A/G]AAGTCATGAAAAACC | 57626 |
rs143835423 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955529 | CTACAGGACCTGACA[C/T]TTTGTTAGTAACTCT | 57626 |
rs143840976 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714244 | TTCTATTTTGACTTA[C/T]GTCATATTTTATTAC | 57626 |
rs143842167 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833185 | CCCACAGAGTGGGAG[-/A]AAAATCTTCACAAAC | 57626 |
rs143846901 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023061 | CATGTTTTTCAGTCA[C/G/T]ACAGACCTTTATTCA | 57626 |
rs143848218 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983624 | AAAAAAAAAAAAGCT[C/G]TGTTTGATGGTAAAC | 57626 |
rs143858661 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743316 | GGTTAGGTGGCGGTA[A/G]GGAGATGATTAGAAG | 57626 |
rs143863293 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945136 | GATTACAGTCACCCG[C/T]CACCACGCCCAGCTA | 57626 |
rs143868675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102924 | GGTAAGGGTAGAATG[A/T]TGAGTAAAACAGACA | 57626 |
rs143888911 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064555 | GATAAACCTCATTGT[C/T]ATGGTTGTAATGTTT | 57626 |
rs143891928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988697 | TGATTTTGATTAGTA[C/T]TTCTCTAATGATTAG | 57626 |
rs143896996 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835189 | GTGAAATAATCTATG[G/T]AGAAAACTGTAGAAT | 57626 |
rs143899199 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993958 | TATAGAGCTGATAAA[A/G]GACAAAGATTTGGGT | 57626 |
rs143899294 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69889044 | TATGTTGCATAGGTC[-/AT]ATATATATATATATA | 57626 |
rs143900108 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69926288 | AAATTCAAGGATTAT[C/T]ATATAGCTTAAGTTA | 57626 |
rs143901855 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827921 | AATGAGCTTGGAAAA[C/T]ACTCTCAAGATAAGT | 57626 |
rs143905328 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902769 | GTAGGGTTGGGGGAG[A/G]GGGGAGGGATAGCAT | 57626 |
rs143912368 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884565 | CTATAGCTAGGCCAT[C/G]AAAATATAGTGAGGG | 57626 |
rs143927475 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724086 | GTGATCCATCTGCCT[C/T]GGCCTCCCAAAGTGC | 57626 |
rs143927949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018342 | TGGCAAAGCTGAGAC[C/T]TGAACTCAAATAGTG | 57626 |
rs143928043 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768821 | CTAAAAGCAAAAATA[A/G]TGCTTGAAATTTAGG | 57626 |
rs143956507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869305 | TCAGAGTATTAAATT[A/G]GAAATTTTGATTTAT | 57626 |
rs143967784 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057950 | ATATTTATCCCAACA[C/T]GTACAAATCAATCAT | 57626 |
rs144008676 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765988 | TAACAGATTCAGCTG[G/T]GGAAGAACATTAAAC | 57626 |
rs144012055 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789284 | CATGTCTGTCTGTCT[G/T]TTATTTTGTATGGGT | 57626 |
rs144014302 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060604 | ATCCAAGCACTTTGG[A/G]AGGCTGAGGCGCGTG | 57626 |
rs144022028 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949200 | TTTACATTCCTTAGA[C/T]TTTTTTTTCTTTTCT | 57626 |
rs144026251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106716 | AAATAATGTTGCTGT[C/T]CAGTGGCCTCATTTT | 57626 |
rs144034488 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794317 | ATAAGACACAAAAAC[C/G]TATCATATGCCTTAG | 57626 |
rs144036082 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036887 | TTAAAGCTAAGCATT[A/C]GATTTCTGTTCTTTA | 57626 |
rs144036455 | in-del | -/TTC | 0.207253 | 0.246318 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997276 | TTCAAATTTTATTTT[-/TTC]TTTTTTATTTTTAAT | 57626 |
rs144049553 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969390 | TAAGACACAGTTATC[C/T]TCAAATATTTATTAC | 57626 |
rs144066955 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774807 | TGAACTGACTACCTA[A/T]GTGTTATCTTTTATT | 57626 |
rs144069519 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798892 | GGCCTCAAACTCTGT[C/T]GAAACCCCATCTCCA | 57626 |
rs144079352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841623 | TATCATTAAAATGAC[C/T]GCATTGCTCAAATCA | 57626 |
rs144082469 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902733 | ACAGAGGAAGGGGAA[C/T]ATCACATATCGGGGT | 57626 |
rs144082506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837011 | TGGGGATTGACTATA[C/T]GACTCTTTATATTTT | 57626 |
rs144096716 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865942 | TATTCTGAGAGTAAC[C/G]AACATTAGCATGAAT | 57626 |
rs144108402 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731677 | ATTGAATTGACAAGT[A/T]GCTATTTGCTTTAGC | 57626 |
rs144136581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819846 | TTTTCTCTGTTTTGG[C/T]TCCAAAGATCAGTTT | 57626 |
rs144137458 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793190 | TGAAATAGTGCATTG[C/T]AGTAATGTCTTATTC | 57626 |
rs144139347 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973681 | AAAAGTATCAGTAAA[C/G]TAGTATCAAATACCT | 57626 |
rs144144141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998626 | CACTTCTACCTCAAT[C/T]AATAACTAGGACCTT | 57626 |
rs144148687 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716957 | CTCTTACTAGGGTGA[G/T]GCTCAGTCAGAAAAT | 57626 |
rs144157909 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901694 | CAATGTGGTTGCAAA[A/C]TAAATTGATGATATC | 57626 |
rs144158064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945659 | TATATGAACAAAAAA[A/T]GCTCAATATTATCAG | 57626 |
rs144163732 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004415 | TTAGCTATGTCCTGA[A/C/T]CCTTTCTTTGGTCAT | 57626 |
rs144165016 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70049772 | ACAATGCGGTGTTTC[A/G]AGAACATCATGTTAG | 57626 |
rs144171952 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822147 | GAGGTTGCAGTGAGC[G/T]GAGATCACCCACTGC | 57626 |
rs144178720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711195 | CTTAACAAATAGAAT[G/T]GAGAATGTTTCTTTT | 57626 |
rs144225252 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921651 | ATTCCTCTGTTTCCC[G/T]TTTACATGCCCTCAC | 57626 |
rs144232509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937742 | TTCGGAATTATTTGC[A/G]CAAATTCAGTAGCTG | 57626 |
rs144232664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893955 | TCACTCTCCAAAAGA[C/T]ACATAGGATGTTTGC | 57626 |
rs144260651 | in-del | -/AAAG | 0.173643 | 0.238054 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826578 | GAGCAAAACTGTCTC[-/AAAG]AAAGAAAGAAAGAAA | 57626 |
rs144270903 | snp | A/C | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955378 | TTCAGTGGCACACAA[A/C]CTTTTTCTACAAGGA | 57626 |
rs144272165 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751340 | CATACCCTCACAGAA[C/T]GCGTACAGGTGGATA | 57626 |
rs144274324 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858280 | GGAGAAAGACTGGGG[A/G]TTGGGTGAGACTCCT | 57626 |
rs144285176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789060 | ATCTATCTATCTATC[G/T]ATCTACTTATTTACC | 57626 |
rs144285686 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103255 | AAAATTATAGGGAAG[A/G]ATATTAAGTCTGGAA | 57626 |
rs144293068 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758271 | ATTAGTGTATTATCA[A/G]TACAAAAGCTAATTT | 57626 |
rs144295610 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031994 | GTTGAGAAAGCCCTG[G/T]GGGTGAATCCTGATT | 57626 |
rs144332338 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993989 | CATTAACTAGATGTT[A/T]AAAAAATGCTTTAGC | 57626 |
rs144337940 | snp | C/T | 0.031825 | 0.122064 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966217 | GAAGTCAATGACTGG[C/T]TTCTAAGCTTCAAAG | 57626 |
rs144339243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755254 | TCCCACTCTTGCCAC[A/G]TGATACACCAGCTTC | 57626 |
rs144341116 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704904 | CTCAATATATCATTA[C/T]CAATATATCTTATAT | 57626 |
rs144347575 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815978 | ATATTTTGTTGGTAT[A/G]TAAAACATATTAATC | 57626 |
rs144354213 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060444 | GAAGAAAATCAATAT[G/T]TTAAAGACACACCTG | 57626 |
rs144357378 | in-del | -/ATATATATGT | 0.0678174 | 0.1712 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020788 | TCTTCATATTGTGAG[-/ATATATATGT]ATATATATGTATATG | 57626 |
rs144367963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778909 | GTTCAAGCAATTCTC[C/T]TGCCTCAGCCTCCCG | 57626 |
rs144373979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071422 | TTACAGACTTCAATG[C/T]ACCTCTGTAATGGAA | 57626 |
rs144375027 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023952 | GACTCCATTAGAAAC[G/T]TATATAGTTTTTCCT | 57626 |
rs144375110 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947042 | GTTGTGTGTGTGTGT[-/G]TGTGTGTGTGTGTGT | 57626 |
rs144385518 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730698 | CACCTCAGCCCCTCA[A/G]CCTCTTAAGTAGCTT | 57626 |
rs144386939 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793546 | CTAGATAAGTCAAAA[C/T]ACATTTTGAGGTTTC | 57626 |
rs144406230 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703306 | ACAAACCTGTTGTAC[C/T]GCTTTTTTGAAAATG | 57626 |
rs144423217 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974105 | ATAAACTCTTTAAAA[C/T]AGTAATGTACTTAAG | 57626 |
rs144424988 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701477 | TACCAATAACCATTC[A/C]CGAACTAACTAACAT | 57626 |
rs144426167 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777934 | ACTTAACAAGTAAAC[A/G]TTCTTAGACAAATGT | 57626 |
rs144453328 | in-del | -/AGAGGAAGA | 0.039522 | 0.134904 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933001 | TACAAAAACAAAAAC[-/AGAGGAAGA]AGAGAAATTTCCTTT | 57626 |
rs144458691 | snp | A/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955708 | AGTGAACCTCAGTGC[A/T]TCCTTTCCAAATATA | 57626 |
rs144459582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028999 | AAAAAAAAAAATCAC[C/T]ATTCCTGATTAGGGA | 57626 |
rs144482558 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007560 | TAGATAATACTGAGA[C/T]TTGAAGAGTTAGCTA | 57626 |
rs144492836 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020693 | CACAAGTCGGCTGAA[A/T]GCATTAAGTGGAATT | 57626 |
rs144493865 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809256 | AAGGCACACAGTCAT[C/T]AGACTATGCAAGGTC | 57626 |
rs144503813 | in-del | -/CCTCCCCTCT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69779372 | TCCTTTCCTTCCTCC[-/CCTCCCCTCT]CCTCCCCTGTCCTCC | 57626 |
rs144526255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957996 | ATTTTAAGTAAAGAA[A/G]CTAACTTCATACCTT | 57626 |
rs144527919 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709917 | ATAATTTATGTAGAA[C/T]ACAGTCTGGATTTTG | 57626 |
rs144537577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914945 | AATACAAGAGAAATA[C/T]ACATGTAAACAACAC | 57626 |
rs144547913 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69840625 | TTGGCTCAGTTTCCT[C/T]TTGTTGTATACTAAT | 57626 |
rs144558237 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774988 | TTGTGGAAGGGGAAA[A/T]GCTTTTTGGAACAAA | 57626 |
rs144565069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802765 | TTAAAAAGGACAGGA[A/G]TTGCTCAGTCAGGGA | 57626 |
rs144575565 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857671 | CATAAGTTGAATGTT[C/T]GTTCTCTGAAGTATT | 57626 |
rs144581433 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981484 | TCACTCTTACATACA[A/T]AGATCTTAGACAAAG | 57626 |
rs144583054 | in-del | -/CA | 0.019137 | 0.0959284 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975811 | TGACAGCCTATAAAC[-/CA]CACACACACACACAC | 57626 |
rs144584696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775539 | ACTGTTTTCTATTAG[A/G]GCTTACATTCTAGCT | 57626 |
rs144593572 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842314 | GAGAGGACAAATACG[C/T]AGAATGTACAGGAAA | 57626 |
rs144607084 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984483 | AAAACTGTTTGCATA[A/T]TAAAAGATTAGGGTG | 57626 |
rs144612585 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754434 | CCGAACTTACCATAA[C/T]ACCTACCAAACATTT | 57626 |
rs144618855 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109320 | AGAACCCAGTAGTCT[C/T]TGTTGAAGGCAAAGG | 57626 |
rs144620558 | in-del | -/AACA | 0.0744748 | 0.178019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810639 | AACTAGAAAAACAAG[-/AACA]AACTAAACAAAGCTA | 57626 |
rs144621870 | in-del | -/ATC | 0.0283406 | 0.115616 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789118 | TATATTAAAATCTGT[-/ATC]ATCTATCCTCTAAAT | 57626 |
rs144624124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923131 | GAACTCCAGATAAAA[C/T]GGGAAGAAGGTTCAT | 57626 |
rs144626242 | in-del | -/ATAG | 0.383053 | 0.211653 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773148 | TTTTGTACATGCATA[-/ATAG]ATATATATTAAATTA | 57626 |
rs144628448 | snp | A/T | 0.107341 | 0.205301 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814964 | TGCAGTGAGCCGAGA[A/T]CGCACCACTGCACTC | 57626 |
rs144633454 | in-del | -/ATAAAA | 0.192715 | 0.243348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943671 | TGTGTATCTGCTGTT[-/ATAAAA]ATAAAGTTAAAATAG | 57626 |
rs144650392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951730 | ATGCTTCATATGTTA[C/T]CTCCTTACCTTGCTG | 57626 |
rs144651665 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722791 | TACAAGTAGATTCAC[C/T]ATATGATCCAGCAAT | 57626 |
rs144655382 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016451 | TCGTAAGTGCCTGCT[C/G]TAGCTCCCTGGCCTC | 57626 |
rs144668173 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882782 | ATGTTCAAGTTTCAA[G/T]TGTACTGCTATATAA | 57626 |
rs144671542 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69963877 | TCTGATGGCAAAAAA[A/T]AAAAAAACATACACA | 57626 |
rs144692946 | in-del | -/GTTTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69964052 | TTTGTCAGTTTGTTT[-/GTTTG]GTTTTTTTAAAAATA | 57626 |
rs144698960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919581 | TCCAAGTAAATGGAG[C/T]CCCTGATGCAACTAG | 57626 |
rs144707731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051472 | TTACTTTGGAAAAAA[C/T]AATGCAGCACATAAT | 57626 |
rs144715712 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984061 | AAATTATTAGAGGTA[A/G]ACATAGGGAAAATGG | 57626 |
rs144731935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878739 | AGAGAGAGAGAGTGA[A/G]AGAGAGAAAGATTGA | 57626 |
rs144734196 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720556 | CTGGGGAAGGTTCAA[A/C]GTGCAAGGGACATAG | 57626 |
rs144739943 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949507 | ATCTTGATCACGTGC[A/G]GAGGTAGTGTATGTC | 57626 |
rs144744758 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69765094 | GTACCTGGGATTGTA[A/G]GCATGTGCCACCATG | 57626 |
rs144744828 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719738 | GATACTCAATAAATG[A/C]TCATATATACTAGAA | 57626 |
rs144746373 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987443 | ATATTTTCAGCTATT[C/G]AATAAAAATCAGCTT | 57626 |
rs144761752 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant, missense, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975755 | TCTTCAGAGCTACTG[G/T]AGTCCAAATCACTTT | 57626 |
rs144783047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088880 | CTTATCAGGGCTATT[C/T]ACGTATTTTTTATTT | 57626 |
rs144785072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789419 | AAAATATGACTATTG[A/G]GTCGAGGAATCTGAG | 57626 |
rs144805559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865784 | TTCTAGGCATTGTTA[C/T]TGGACATGGAATAAG | 57626 |
rs144805651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023640 | CCTCATTTACATCCT[C/T]CAAACTTTCCTTTCT | 57626 |
rs144811018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937274 | TGAACAGAGAATTGC[A/G]TTAGTAAAATAAATT | 57626 |
rs144817501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724246 | GCATGTAATGGTTGA[G/T]GTATTACGTCTCCAT | 57626 |
rs144822827 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011327 | CTGTCAACACAGATA[A/T]TATAAATTATACAAA | 57626 |
rs144830050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980636 | TACAGTTTAAATATC[A/G]CTACCTTCAGAAAGC | 57626 |
rs144836927 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936652 | ATGTTGAAGCATGTT[C/T]TGAATTTTTTTTAAT | 57626 |
rs144838688 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766493 | ATATACATATATATA[C/T]ATATTTAGAGTGCTT | 57626 |
rs144867124 | snp | C/G | 0.000878202 | 0.0209363 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107689 | AAGTCTTTTCGCCCA[C/G]AGCCTGACATGCTTT | 57626 |
rs144871900 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046004 | TCTAGTTAAGTTGTT[G/T]TTTGTAATTTATTTA | 57626 |
rs144881134 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864990 | CTTGCTCTGCTGTCC[A/G]GGCAGGAGTGCAGTG | 57626 |
rs144885488 | in-del | -/ACTGATATATTTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69968327 | TATCATGTAAATAGA[-/ACTGATATATTTG]CTAAGAAACAAATAT | 57626 |
rs144895338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823414 | GGGGTTGTTGGTGAG[A/G]CGTTAGGCTCTAAAG | 57626 |
rs144897426 | in-del | -/TCTCTCTCTCTCTC | 0.478685 | 0.10101 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024621 | TGAGGAGAAAAGATT[-/TCTCTCTCTCTCTC]TCTCTCTCTCTCTCT | 57626 |
rs144908760 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826656 | TATTTGAGGCAATTT[A/G]TATGTTAATTATCTT | 57626 |
rs144929664 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096631 | GCTTGTCAGGAATAT[A/T]TTATAAAGTTAGCTG | 57626 |
rs144930586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897534 | TTATACTTGCCTTCA[C/G]AATAAATGAGAAAAT | 57626 |
rs144951866 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69994820 | AGGAAAAATTTTTTT[A/T]AAAAATACTAATATA | 57626 |
rs144956765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722396 | CATACAACCTACCAA[G/T]ACTAAATCATGAAGA | 57626 |
rs144957449 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787547 | TGTTAGACCTAAAAC[C/G]ATAAAAACCCTAGAA | 57626 |
rs144958985 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69722104 | CATCTTTCTGTGAGA[C/T]ACCTAGCACAGCTCT | 57626 |
rs144960641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927457 | AAAACACTTTCTCAT[C/T]AGGAAAGTGAGAAGC | 57626 |
rs144962153 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936775 | GGAAGTTTCTACTGA[A/C]GATTTCAACCTTCAT | 57626 |
rs144965631 | in-del | -/A | 0.0766824 | 0.180169 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776157 | GAGACTCCGTCTCGG[-/A]AAAAAAAAATAAAAA | 57626 |
rs144972318 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69765030 | AATCTCAGCTCACTG[C/G]AGCCTCCACCTCCCA | 57626 |
rs144974501 | snp | A/C | 0.127254 | 0.217792 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787163 | GGAAAAAACTACTTT[A/C]AAGTTCATATGGAAC | 57626 |
rs144989576 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996264 | GCCAAGATCGCACCA[C/T]TGCACTTCAGCATGG | 57626 |
rs144994824 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787354 | CCTCAGAAATAATGC[C/T]GCATGTCTACAACCA | 57626 |
rs144998924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859088 | GCACTGTATAAAACT[C/T]GCAATTTTACCTTCA | 57626 |
rs145000923 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899410 | AATTGTGTGGCAAGG[C/T]CATCCTCTGCATAAG | 57626 |
rs145001040 | in-del | -/ATAG | 0.0988009 | 0.199095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882017 | GTATGATCACATTTT[-/ATAG]ATAAAGAGATTGAAT | 57626 |
rs145017192 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025377 | TCAATATAGATTCTC[G/T]GATATTTTACTTATT | 57626 |
rs145022797 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895847 | TAGTAGGTGAGACTA[A/C]ATGTGTGCACCACCA | 57626 |
rs145024395 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996075 | TTTGGGAGGTCAATG[C/T]GGGAGGATCATGAGG | 57626 |
rs145040798 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767564 | AAAAACAGTAAATAT[C/T]GGTCTATACTAATAT | 57626 |
rs145042320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033962 | AAGCCCTAATACGGA[C/T]GAAATATAAAATCAT | 57626 |
rs145049894 | snp | C/G | 3.74869e-05 | 0.00432921 | synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107649 | GAAGAGTTTCCAGCG[C/G]AGTCGCAGAATGTGC | 57626 |
rs145056251 | snp | A/T | 0.0898077 | 0.191933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831282 | TACAACTGATAACAC[A/T]GAAATAGAAAAGATC | 57626 |
rs145063187 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966842 | GCTTTTAGCAACTAC[G/T]TATGAGTGAAGACAT | 57626 |
rs145065900 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104196 | TGTATATTTAGACAG[A/G]GAAGTAGAGAAATTA | 57626 |
rs145086788 | snp | A/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958765 | ATACATATTATCAAA[A/T]GGCTGGACTTTTACA | 57626 |
rs145089611 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780084 | AAGTGCTGGGATGAC[A/G]GGCATGAGCCACCGT | 57626 |
rs145099020 | in-del | -/AT | 0.134795 | 0.221873 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834296 | ATTACAATTAGTTAA[-/AT]ATATATATATATGTA | 57626 |
rs145108959 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903788 | CTGGGATTACAGGTG[C/T]GTACCACCATGCCCA | 57626 |
rs145123710 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996029 | CTTGAAATAGGCCTG[A/G]CGTGGTAGCTCACGC | 57626 |
rs145127084 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102344 | TTTGCATATTGTTTA[G/T]TAATTATAAAATAAA | 57626 |
rs145131237 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030484 | TGAAAAACCTGCTCC[C/T]GAATGACTACAAGGT | 57626 |
rs145144048 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897469 | AAAAACTATATAGAA[C/G]ACTTAGAGATTGATC | 57626 |
rs145155899 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810500 | CAAATGAAAATAGAG[A/G]CAACATTCCACAACC | 57626 |
rs145161183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880980 | CCCCAAAAGATTACC[C/T]GCCCAAACTCTAATA | 57626 |
rs145162982 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776433 | AACAAACTAATTAAT[A/C]TTTCTAGTTCTCAGT | 57626 |
rs145170424 | snp | C/T | 1.65051e-05 | 0.00287267 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107276 | CTTGCAGAACCAGCC[C/T]TTTTTCGTGTGGTCC | 57626 |
rs145179732 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104001 | TGTAAGAATTCAGAA[G/T]CTAAAAAAGCAAGCA | 57626 |
rs145188294 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744936 | AAAGCTGCAATGTAC[A/T]CTTTCTTGATGTACA | 57626 |
rs145189998 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700800 | TAATCATAAACACTC[A/C]AACTTAATGGATCAT | 57626 |
rs145190547 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103595 | GTAGCTTAGATTAGG[C/T]GCAGACAATGGCTGT | 57626 |
rs145190820 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808274 | CAAACATACCCTGAG[A/G]GAGGGTGCTTTTCTT | 57626 |
rs145193721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004914 | TATTTTGTAGAAAAC[C/T]ATATATTTATGTTTA | 57626 |
rs145196482 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905137 | ATTCCAAGGTTAGGA[C/T]AGATTATGTTTGTCA | 57626 |
rs145208547 | in-del | -/AAT | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036064 | TCTTACATTTGAGGA[-/AAT]AATAATCATACTTCT | 57626 |
rs145209433 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745657 | ATATAAAAATTAAAA[C/T]AATAAACTTTTCAGA | 57626 |
rs145210328 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994579 | TATCACACATCAAAT[A/T]AATTACAGTATTGTA | 57626 |
rs145212803 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809422 | CATTCTTAAAGCAAA[G/T]AAATGCCAGCCAAGA | 57626 |
rs145218874 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837616 | TACATCTCTCTCTCT[A/C]TATATATGTGTGTGT | 57626 |
rs145240106 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994052 | ATTGAGAATGTACAA[A/G]GGACTAATGATAAGC | 57626 |
rs145241208 | in-del | -/CATT | 0.45574 | 0.142025 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950363 | TCAGAGTAAAAGCAA[-/CATT]CATTCCCTTGACTCA | 57626 |
rs145263602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851512 | AGACATTTTTGACTT[C/T]AGAGTTGCATGAAGT | 57626 |
rs145268047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065115 | ATTTCAAGACCAGAG[C/T]CCCCAGGAACAGTGA | 57626 |
rs145268106 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105995 | TTAAAAAATATATAT[A/G]ATGTATATAATTGAA | 57626 |
rs145280706 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844361 | TATGAATAAAATATT[A/G]TGTAAAATGTAACTT | 57626 |
rs145288722 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952856 | TGAAATGACAGGGTT[A/G]TTTTGCTTGTTTATA | 57626 |
rs145288884 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913393 | TGGCCACTGCTCCTT[G/T]CTCAGCAGGGGAGAG | 57626 |
rs145290491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846372 | ATGACCAGGAAATAT[A/G]TAGGATAAACTCACA | 57626 |
rs145320191 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739858 | TCCCAGGGGATAGTA[A/G]ACAATATCTGGAGAT | 57626 |
rs145320500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802886 | GGCTTGTCCTGCTAC[A/G]TTTCTGGGTTCCTAC | 57626 |
rs145328938 | snp | C/T | 0.000532056 | 0.0163017 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107222 | GTCCACATCCTTCAC[C/T]TGTTGCCTGGCTAGA | 57626 |
rs145331399 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803617 | GCTGGCCTTGATGAC[A/G]TGATCCCCTGAAAGT | 57626 |
rs145332486 | in-del | -/A | 0.178465 | 0.239547 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704193 | CCTTTCTGTTTTTTC[-/A]AAAAACAAAATGTGA | 57626 |
rs145333209 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879728 | CAAATATGAAACCAA[A/C]CCTAAATAAAAAATT | 57626 |
rs145345175 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950147 | CTGTTAGAAAAGTCA[A/G]AAAAGGCTATGCAAA | 57626 |
rs145356053 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69944978 | TAAACTATAAAACTT[-/C]TTTTTTTTTTTTTTT | 57626 |
rs145371905 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751640 | ACAATAAGGCTAAAT[G/T]GTTAAAAGACCATAC | 57626 |
rs145374447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921561 | ACGTGGCCATACCAA[C/T]GCATTGTGAAGACAA | 57626 |
rs145374474 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875204 | ATTGATTGAAGTGGA[C/T]TGAAGAGAGAATGAT | 57626 |
rs145378724 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843004 | ATTATATGGAGGTAG[A/G]GAGTTGAAAGACAGA | 57626 |
rs145388121 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893680 | TACAAAACATAAATG[C/G]GTGGAGCATTAATAT | 57626 |
rs145391192 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092264 | AAAAAATGAATACAA[C/G]TTTCTAAACTATTGT | 57626 |
rs145393484 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958148 | CTAAGTATTAACCTT[C/T]ACATATTTTTTTCTT | 57626 |
rs145407239 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69727037 | TTTGACAAATGGCAG[A/G]GAAAATTATTAATTA | 57626 |
rs145411717 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052143 | CTCCTGGTAAGCAGC[A/G]CAAATTCTGATGCAC | 57626 |
rs145415248 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791510 | ACCAAAGACAGTGTG[A/T]TCACACTACATGATT | 57626 |
rs145417021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984203 | TAGGCAGATAGTGAG[G/T]GTACGGATGTCCTTG | 57626 |
rs145419242 | snp | A/G | 0.474182 | 0.110646 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783758 | TGGAAAACACTCTGC[A/G]GGATATTATCCAGGA | 57626 |
rs145432312 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087725 | CTTTTGGAAACAAGG[C/T]CTTCTGATGGAGTAA | 57626 |
rs145439723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977142 | GATTTCTTATACACA[A/T]TGCCTGGCATTAAAG | 57626 |
rs145460992 | snp | A/C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916603 | TGTGGAGTGGGGGGA[A/C/T]GGGGGAGGGATAGCA | 57626 |
rs145477849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980176 | GAAACCTGTTTCCCT[A/G]TTTCTTTGTTAAACA | 57626 |
rs145487050 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791400 | TCAATATTTAAATCC[A/C]AGGTACCCTTTTGTA | 57626 |
rs145494192 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863856 | TCTCACTAATATTTT[A/C]ATAATTTATTTAGGC | 57626 |
rs145496884 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70048871 | GTTGGGGACCCCTGC[C/T]ATAAACAATACTTTG | 57626 |
rs145499177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061301 | TTAAAAGCCTTGGGT[G/T]TTGTCCTTACTCCCC | 57626 |
rs145501825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763310 | GACTCAGTTGCAGGA[A/G]GTTAATAAACTAGCT | 57626 |
rs145507058 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897984 | ACAAATTCCTCACCA[C/T]GGAAAAAGTAGTCAT | 57626 |
rs145509669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771100 | ACTTTTGGGCTTTAC[C/G]AACCTTTTCTTCTCT | 57626 |
rs145517676 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021667 | TTCCACGTCCTTGCC[A/G]GCATTAGAGTTCTGG | 57626 |
rs145520617 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759805 | TAAATATTGTATCGT[C/T]ATTTGCCCAAACCAA | 57626 |
rs145529079 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956981 | TTTGAACATAGAGTG[A/G]TAAGATATTGTATGA | 57626 |
rs145551761 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827675 | GTCAGAGGTTTCAGT[A/G]AGCCAAGATCGTGCC | 57626 |
rs145556981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010122 | AAAGAGAGTGCAATA[A/G]AAGATAAAGTCAAGA | 57626 |
rs145563664 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788350 | AAAATAAAGAGTTCA[C/T]GTCCTTTGTAGGGAC | 57626 |
rs145564626 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830807 | CAAACCCTCAAAATC[A/T]TGCACATAGATGGAA | 57626 |
rs145565176 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901489 | ATATGCTTGGGTGAC[A/G]ATGATGACTCTGGTC | 57626 |
rs145590873 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69744088 | CAATTATATGGCTTT[-/T]AAAGTCGTAGTCCTA | 57626 |
rs145592617 | in-del | -/TT | 0.150667 | 0.229419 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720288 | CATGATTTGAATACA[-/TT]GTTTAATCCTAATAA | 57626 |
rs145597626 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795232 | TCTTTCCTTCTCTCT[C/G]TCTTTCCTTTTCTCT | 57626 |
rs145602663 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066254 | CATATTAAGCAAGGG[C/T]AAAGTTACTAATTTA | 57626 |
rs145604618 | in-del | -/TAC | 0.0558544 | 0.157504 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099158 | AAGTTTTTTAAGTTT[-/TAC]TACAATTTAATAATA | 57626 |
rs145605137 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083205 | AAAAATGAATCTCAA[C/T]AAATATTAATCAAAA | 57626 |
rs145610116 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723082 | CAGGCACAGAAAGAC[A/T]AATACCACATTATCT | 57626 |
rs145628285 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965276 | CATGGGCTCACTTCA[C/T]GTATCTTGGTCACAT | 57626 |
rs145635233 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789760 | TCCTCACCTTGAAAA[C/G]GTAAGGCCAATAGTG | 57626 |
rs145661740 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967816 | CTTGAACCTGGGAAG[C/T]GGAGATTGCAATGAG | 57626 |
rs145661784 | in-del | -/ATAA | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730478 | AACCGACTGTTACTT[-/ATAA]ATAGTGATTAGAAAA | 57626 |
rs145682111 | snp | A/T | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996476 | AGCTGATACTCCAGA[A/T]GTGATATTTTTACAT | 57626 |
rs145694020 | snp | A/C | 0.00105105 | 0.0229002 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107609 | CTCCCCCCGCCGGGC[A/C]GCCGGTGGAAGGAGA | 57626 |
rs145701655 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073350 | ACTCATAGGTGGGAA[A/T]TGAACAAGGAGAACA | 57626 |
rs145702222 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759104 | CTCCCAGCAGGGAGG[A/C]AAATCTGGGCCGAGG | 57626 |
rs145706440 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042160 | TATATAAGGAAAAAA[A/G]TGAAACCAACAGAAA | 57626 |
rs145714027 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943145 | CTTGTACCCTGCTCC[A/C]TCATGATCAAGAGGC | 57626 |
rs145724452 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715418 | CATATAAGACATGCC[C/T]GCTTCCCCTTCTCCC | 57626 |
rs145728308 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779493 | GTTGCTTTCCTTTTC[C/G]CTTCTTTCCTGTCCT | 57626 |
rs145734248 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871991 | TTTCAGGAATCTTTA[G/T]AGCAACACTGACTCT | 57626 |
rs145741254 | in-del | -/TCTT | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789965 | CTGAAGCATCCAGCG[-/TCTT]TCTTTCCATAGAAAC | 57626 |
rs145752017 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746492 | ACACTAAGGTTCTTT[C/T]GGTTACAATGTGCTA | 57626 |
rs145761717 | in-del | -/TATAAAC | 0.313814 | 0.241719 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958453 | TATTTTTTCAAAGAT[-/TATAAAC]TATAATCATTGAAGC | 57626 |
rs145765930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082586 | TCCCCAGAACATTTT[A/G]TAGCCAGTTAAACTA | 57626 |
rs145773887 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812580 | ATCTACTCATCTGAC[A/G]AAGGGCTAATATCCA | 57626 |
rs145788042 | snp | A/T | 0.0138799 | 0.0821421 | | | GRCh38.p7 | 13:69718771 | AAGGTGTCATCCCAC[A/T]CTAGCTTCTATGCAC | 57626 |
rs145788220 | snp | A/T | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 13:69980712 | AGATTCAGGGGATAG[A/T]TGTGCATTTGTTACA | 57626 |
rs145807810 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917297 | GGATTCCTAAAAACT[A/G]AAACTAAAATCAACC | 57626 |
rs145813925 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69876659 | ACTCACAAACACACA[C/T]ACACATTGCTATATA | 57626 |
rs145821685 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931829 | GGGAAATTATGTTAC[C/T]TGTTAAAAAGTTTTG | 57626 |
rs145834254 | snp | C/G/T | 8.9087e-05 | 0.0066736 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107186 | ATGCTTGGAAGCCCC[C/G/T]TGGGGACTTACTGTA | 57626 |
rs145843851 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70057806 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA | 57626 |
rs145849497 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930893 | TTTATGCATATATGC[A/G]TTAATCAGTGACTAC | 57626 |
rs145852786 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917787 | CACATAACATTCCAC[A/G]TATCTTTTGAAGTCA | 57626 |
rs145853660 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754083 | CTGGGCTCAAGCAAT[A/C]CACCTGCCTCAGCCT | 57626 |
rs145855361 | in-del | -/ATA | 0.463559 | 0.129972 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805168 | CATTTCTAAATCATT[-/ATA]ATAATTCCAAATGTG | 57626 |
rs145861949 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814618 | AACATACATGTGACC[A/T]AGAAACATAAAAAAT | 57626 |
rs145868755 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70088887 | GGGCTATTTACGTAT[C/T]TTTTATTTGGGAAAA | 57626 |
rs145872706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015620 | ATTACATGAGATGTT[G/T]AATATTTTATTATAA | 57626 |
rs145879598 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818463 | TGACCTCGTGATCCA[C/T]CCACCTCGGCCTCCC | 57626 |
rs145901697 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69806270 | ACAACTTGATAAATG[C/T]TTGCTTCTGTTCTCT | 57626 |
rs145914955 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025618 | AAAGTAAATTAGGAG[A/T]TGCTATCTGAATTCA | 57626 |
rs145918968 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742387 | AACTTGACTTTAAAG[A/G]TGTGCAGAAATATGA | 57626 |
rs145948986 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806998 | ACATGCCTTGGTGGT[A/G]CTCTGACCCTGTCTA | 57626 |
rs145949114 | snp | C/G/T | 0.00398691 | 0.0444912 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770165 | CTGAGTTTTTAGGCA[C/G/T]CACTGCATTCCCCTC | 57626 |
rs145957986 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870936 | TGCTTGCAACTCTTC[C/T]AGGCTGAGGTGCAAA | 57626 |
rs145974845 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802564 | TGGTAGTTAAAGATC[A/G]ACCCCTGACCTAATC | 57626 |
rs145976703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873065 | AACTTATTTTTACTC[A/G]TATAGTGTTATTGTC | 57626 |
rs145983235 | in-del | -/TGTCATACAA | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943199 | TTTGGTGGCTTTGAG[-/TGTCATACAA]TGTTTTAGGCAGTAT | 57626 |
rs145999758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080873 | CCCAAAGTGCTGGGA[C/T]GTGAGCCACCACGCC | 57626 |
rs146012761 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974901 | AAATAAAATCAATAA[C/T]ATAAAAATGCTTTCA | 57626 |
rs146013538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857316 | TTCCCTGATGCCAGG[A/G]CATATTGACTACTCC | 57626 |
rs146014351 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909688 | AAATAATTTTTGGAA[A/G]AGACCCTATAATTTA | 57626 |
rs146028386 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757754 | GTCAGGAGTTTAAGA[C/T]CAGCCTGGCCAAACC | 57626 |
rs146032923 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927620 | ACATTTCTCCAAAGA[A/G]GATATATAAATGTCC | 57626 |
rs146034143 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079221 | CCATGGTAGTTATAC[C/T]TGGTTGACCCTGAGA | 57626 |
rs146035272 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69754015 | CTAATTTTTTTTTTT[G/T]TTTTTAGTAGAGATG | 57626 |
rs146036287 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004557 | TTTTTTTGTATTATA[C/G]TCTTTGTTGATTATT | 57626 |
rs146051723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717870 | TAGTTCCTGATTTCC[A/G]TGGACTAGAAAATCT | 57626 |
rs146053367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892305 | ACAATAACACACCTA[A/T]GTGTTGAGGTCTGTT | 57626 |
rs146065610 | in-del | -/T | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757162 | TACTTATCAGAGTCC[-/T]TTTTTTATCATTTCC | 57626 |
rs146068146 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081642 | GAGACACTCTCTCTA[C/T]TAAGATAAATTCTTT | 57626 |
rs146068154 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783306 | GCTCCTCACCAGCAA[C/T]AGAACAAAGCTGGAT | 57626 |
rs146077129 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816190 | GTTGACATTAAATCA[A/G]TGCAACATTTTAGGA | 57626 |
rs146079740 | in-del | -/TATC | 0.465263 | 0.127129 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001657 | GGGATATCTATCTAT[-/TATC]TATCTATCTATCTAT | 57626 |
rs146079890 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888344 | TACTATATTTAATAT[G/T]AACCCAAGAATATGA | 57626 |
rs146080637 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933304 | TACTAATGTATCATG[G/T]AATAGTCTTGAGAAA | 57626 |
rs146081726 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957647 | TTTGAAAAACTGATA[C/T]ACAATTTTATAAGTA | 57626 |
rs146097196 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820448 | TATCAAGTTCATGCA[A/C]AGGCTTTTGTGTTTA | 57626 |
rs146105598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065795 | ACCTGAACATCAGTT[C/T]ATGTAAAGGCTTAGC | 57626 |
rs146108154 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028647 | AGATATTAATGAGGG[A/G]ACAATTTTTCAGGGA | 57626 |
rs146110876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023019 | CATATCCTCTTAAAG[C/T]GTTCCTCTGGTTAAA | 57626 |
rs146110905 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771803 | TAATGGTGTAATATT[C/T]GTCTTTTACTCTGAA | 57626 |
rs146121682 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098713 | TTAGTGTAGTGAAAA[C/T]TGGATATAAGAAATG | 57626 |
rs146135923 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69991442 | GCTAGCTAGACTAAT[A/G]AAGAAGAAAAGAGAG | 57626 |
rs146137755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929169 | ACCATTTTGGCGATC[C/T]TAAACAAACTTCATT | 57626 |
rs146150987 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773985 | ATTCAATGTTATTTG[C/G]TAATTATTTTTCACA | 57626 |
rs146158512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024125 | TCAGGATGGTATGGC[A/G]TAGACGATTGTTGAT | 57626 |
rs146163991 | in-del | -/CT | 0.280256 | 0.248162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706880 | CATCTTCCCATCACA[-/CT]CACACACACCAACAC | 57626 |
rs146176205 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908065 | TATACTAAATATCAG[C/T]AGTTGTCATATACAG | 57626 |
rs146176650 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70057470 | AGACAAAGACACATC[-/AA]AAAAAAAAAAAAAAA | 57626 |
rs146191150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099285 | AATTTACATTGTAAA[A/C]TTCTGCCCCATTAAT | 57626 |
rs146192954 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798525 | GGAAATTATTGTTAT[A/T]GTTAGGATAAAAATA | 57626 |
rs146228337 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044504 | ACATGAAAAAATACA[C/T]ATAACATTTTAATGT | 57626 |
rs146231596 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979216 | TAGATTTTTTTCCTA[A/C]AAGTTCTTAGGCATT | 57626 |
rs146238672 | in-del | -/TA/TG | 0.164546 | 0.234942 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798097 | TCCCAAATGTTTATA[-/TA/TG]AGATAATATAAGCTA | 57626 |
rs146243978 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945252 | TGCTGGGATTACATG[C/T]GTGAGCCACTGCACC | 57626 |
rs146255439 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873983 | ACATTTAAGCTGAAA[C/T]GTGATTAATAAAAAG | 57626 |
rs146267782 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720270 | GCATCATAAATGGTA[C/T]TAACATGATTTGAAT | 57626 |
rs146277031 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086443 | CAAAAATTAGCCTGG[C/T]GGTGGTGGGCACCTG | 57626 |
rs146277260 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041782 | TCTCCACTGATTGAT[C/G]GGGAGTGGGAGGGCT | 57626 |
rs146280179 | snp | C/G | 0.00100558 | 0.0224004 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975600 | GAATGCATGTTTCCA[C/G]TAGAGGCAGACTACT | 57626 |
rs146293469 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754773 | CTTACACCATTGTTC[A/G]AGTCTTATTTTTGTT | 57626 |
rs146303890 | snp | A/C | 9.99134e-05 | 0.0070673 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69839037 | AGATTTTCTGGGTTT[A/C]GTTCTCGGACTTTGC | 57626 |
rs146306772 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733784 | ACAAACACATTTGAG[C/T]AGTATCTACTAAAGC | 57626 |
rs146319458 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895998 | CAGGCATGAGCCACC[A/G]TGCCCAGCCAGGAAA | 57626 |
rs146322560 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961870 | AAATAGTATTTTTAA[A/C]TTAGAAATATGTCTT | 57626 |
rs146335533 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786590 | CATTCCGTTTGAAAA[C/T]TGGCACAAGACAGGG | 57626 |
rs146338977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858111 | AAGTTCGATTTAGAC[A/G]TCAGTGGGCACCAGC | 57626 |
rs146349825 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69745273 | TTGTGAAGGCCTGTT[A/T]AAAACCTCTTCATTT | 57626 |
rs146350264 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993671 | TCAGGCCTAGAGGTA[G/T]TAATGGACTCCATTT | 57626 |
rs146357172 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093840 | ATTTGGCAATTAGAA[C/T]TGCAGTTTTACTGTG | 57626 |
rs146364208 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063515 | CATGTTATTTTGTTA[C/T]TTAAAATTATAATCT | 57626 |
rs146389179 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738302 | AAAGAATCTACACAC[A/C]AAAATGCTGAAAACT | 57626 |
rs146396196 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70102665 | GCCTTATTAATAACA[A/G]GTCTGTGATTCTAGG | 57626 |
rs146397845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060503 | ACAATAGCCAAAATT[A/T]GGAAGGAAAACCTAT | 57626 |
rs146399675 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991810 | CATTCTATGAAGCCA[C/T]TCAAGTGAGAGCCAG | 57626 |
rs146420522 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060705 | CAAAAAATTAGCTGG[A/G]CATGGTGGTATGCGC | 57626 |
rs146420977 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016364 | CTGCAGCAGCCCAGC[A/C]CAGACTCTGGACCAG | 57626 |
rs146422840 | snp | A/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952869 | TTGTTTTGCTTGTTT[A/T]TATTTGCTTGTTTTC | 57626 |
rs146426298 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956579 | ACTCGTATCATAACT[A/G]ATACCCTATAAAAGT | 57626 |
rs146440146 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764629 | TGAAGCCAATGTAAG[A/C]CTTTGGGAGAAAGTC | 57626 |
rs146447708 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081078 | AATTATGCCATGTCC[-/T]CTTTAAAACACACAT | 57626 |
rs146455026 | snp | A/C/T | 0.00716912 | 0.0595216 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058136 | CAGGTAGTATCATAC[A/C/T]GAATGCAGAAAAGCT | 57626 |
rs146458526 | snp | A/C/G | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766809 | GAAAAGATAAAACGA[A/C/G]GTAGCTAGCTGTAGA | 57626 |
rs146468102 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946259 | TATATTCATTACTTT[A/G]TGGTGAGTATATACA | 57626 |
rs146474020 | snp | A/C | | | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970099 | TTAACCCTCTCACTG[A/C]CATAGGTTTTGTTCA | 57626 |
rs146480207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791544 | AAAACTACTACAAAG[C/T]TTCAGTAAACAAGAA | 57626 |
rs146481317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864758 | ATGTATGCCAAATAT[C/T]GGAGATGAAAATCTT | 57626 |
rs146491338 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721941 | TCATTCACTTACAAG[-/T]TTTTAATCATTCTAA | 57626 |
rs146498671 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794529 | AAAAAAAGAGGAGAA[A/G]AAGGATGAACAACAG | 57626 |
rs146500842 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866839 | TAATAAGAGGGCTTC[A/G]TAATTCAGAACACCA | 57626 |
rs146509174 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901839 | TCTCGCTCTTGTTGC[C/G]CAGGCTGGAGTGCAA | 57626 |
rs146509589 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076210 | GGTAAAGTCGGAGGA[A/T]TGACACTACACAACT | 57626 |
rs146517627 | in-del | -/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69890646 | TTCCACACACACACG[-/CA]CACACACACACACAC | 57626 |
rs146541523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832761 | TATAAAAATAGGCAC[A/G]CAGACAAATAGAACA | 57626 |
rs146541688 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876484 | AATAGAGACAGCATC[G/T]GTCTTCTAAAGTTAA | 57626 |
rs146544839 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079582 | GACTAATGTTTTTGA[A/G]ACCACTTATATACCT | 57626 |
rs146555937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037419 | GTATTGCAATTCTGG[C/T]CTGAACATTTGGTTG | 57626 |
rs146558317 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971807 | CAAGGAAAAACATTA[C/T]GTTTTATAATCATTA | 57626 |
rs146561518 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772556 | TGAATTAAACTGTGC[A/C]CCTGTTTTCTAAATC | 57626 |
rs146563266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838415 | TTGGAGATTTTTCCA[A/G]TAACTCTAAAAACGT | 57626 |
rs146567325 | in-del | -/GT | 0.485491 | 0.109584 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934945 | TTTGTAAAATTTACC[-/GT]GTGTGTGTGTGCATG | 57626 |
rs146568047 | in-del | -/T | 0.0865458 | 0.189163 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775693 | CTGAATGCCTAAGGG[-/T]TTTTTTTTTGTTTTT | 57626 |
rs146576407 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706651 | CACTGCACTCCTAGA[C/T]GGAAACTATTTATTT | 57626 |
rs146578530 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077086 | CTTAAAAAGCTTGAC[A/G]TAATTCTACCAAATG | 57626 |
rs146580936 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712040 | TGAAGAGTTCTTGTT[A/C]AAATCTTCTGCCTAG | 57626 |
rs146601723 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810400 | AGTTCTCAAACCATA[C/T]GAATACATGTATATT | 57626 |
rs146603431 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69926008 | ATTCACTAATTAATG[C/T]TGGACCTCCTTTCAA | 57626 |
rs146619467 | snp | A/G | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813359 | GGGATAGCATTAGGA[A/G]ATACACCTAATGTAA | 57626 |
rs146620473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883991 | TTTAGTATAAAAACT[G/T]CAGTAGAGTGACACT | 57626 |
rs146625243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852621 | TTTTAATCACTTTAT[A/T]TTTGCAGATTTCCAG | 57626 |
rs146628512 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922829 | AACTGTAGTTAAAAA[G/T]GTCTATTCCTTAAGT | 57626 |
rs146661967 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053336 | GTTAGGGCCAGATCT[A/G]GAGAGCATAATATGT | 57626 |
rs146662351 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096092 | TTTATCCATTTGTCC[A/C]GTGATCAACACTTAG | 57626 |
rs146665242 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984578 | GTAAATCAGATACTG[C/T]CTCCTCTAGCTAGTC | 57626 |
rs146673618 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057149 | ATTAGAGACTGCTGA[A/G]AGCAACTATATGCCA | 57626 |
rs146676101 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988770 | GTCTTCCTTTGACAA[A/G]TGTCTTCATGTCTTT | 57626 |
rs146684288 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043147 | CGACCTCTGGTGATC[C/T]ACCTGCTTGGCTTCC | 57626 |
rs146694932 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69725222 | TCCTGAAAATATGTT[A/G]TGAAAAACAGTCACC | 57626 |
rs146695637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092431 | ACTCTCTCTTTAAAA[C/T]AATATATTAAACTCT | 57626 |
rs146697476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731470 | TAACTCCTTTTCACT[G/T]CTACACAGCAGCCTT | 57626 |
rs146707405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977697 | CTAATACACTGATTT[A/G]GAAAACATTATATTT | 57626 |
rs146718646 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941473 | AGGAAAGTTTATAGC[A/G]ATAAATGCCTATAAA | 57626 |
rs146719658 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871217 | AGCAGTACCCAGGGT[C/T]CTTTAAACCACAGCT | 57626 |
rs146722310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942730 | AGAGCTACTTTCAGC[C/T]ATCACATGTCACCCC | 57626 |
rs146738833 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830155 | CCCACATAAAAAATA[C/T]GGAATGGATAATAAT | 57626 |
rs146746396 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867689 | TAAAAGAGAGGGTTT[A/G]TAAGTATATTAAAAT | 57626 |
rs146782988 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109636 | TGATTTATGCCACAA[C/G]AGCTGGACTGCAATC | 57626 |
rs146785739 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996324 | TAAAATAAAAAAATT[A/T]AAAAAAGCCTTGAAA | 57626 |
rs146813808 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746446 | CTACACTAAGAATTA[C/T]ATAAACTCTGATTTA | 57626 |
rs146819254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751251 | TCAATTTTATTGTTA[C/T]GCAACTTGCATTTCA | 57626 |
rs146831216 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106982 | AATTGGTGGCTACAA[C/G]TTTGAAAACTTCCAA | 57626 |
rs146832009 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872575 | CTACATGCAATGATG[C/T]ACCCTCTCCCCTCTC | 57626 |
rs146842461 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889024 | CTTAAGAGTAAGGCT[A/G]CATATATGTTGCATA | 57626 |
rs146842596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848302 | CTTCATTAGTGACTA[C/T]TTGAGTAGATGTGAT | 57626 |
rs146844330 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955604 | ATCAATGAACACAGT[A/G]TATTTTCAAGTATGT | 57626 |
rs146856235 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69944784 | AATAACAAAGTGAGA[A/G]TAAGAGCACTACCTG | 57626 |
rs146857914 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782338 | TGGGTGCAGCGCACC[A/G]TGTGCTAGCCGAAGC | 57626 |
rs146886868 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952786 | AAGCATAATGGGAAA[A/G]TGGACTCTTCATTAA | 57626 |
rs146899680 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973857 | TTGGGAGGTCATTAG[A/G]CTGAGACATCTCCAG | 57626 |
rs146910299 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083610 | AACAGGGTATATGCT[A/G]TCTAAATTATATGAG | 57626 |
rs146910673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039830 | ATTTTTAGTACAGAT[A/G]GGTTTTCACCATATG | 57626 |
rs146917099 | in-del | -/C | 0.234401 | 0.249513 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851141 | TATAGGTAGCTGTCT[-/C]TTTTTTAAGTACTGT | 57626 |
rs146922567 | snp | A/C/G | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754031 | TTTTTAGTAGAGATG[A/C/G]GGGTGTACCTTTGTT | 57626 |
rs146923505 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69848451 | CTTTTAGCTTCAGTT[A/G]AAAATAATTTTGGCA | 57626 |
rs146929590 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108003 | ATGCCCGCGCGAGAG[C/T]CCCGTGTTATGGCGA | 57626 |
rs146942335 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043838 | AGAATCTATGCCCAT[C/T]GTTAAACAGCACATG | 57626 |
rs146956538 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894814 | AATTTCTGGGATTTG[A/G]TTGGCCAATCCTCCA | 57626 |
rs146956959 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854064 | GGCAAAATTTAACTT[C/T]GGAAATGATTTTGAT | 57626 |
rs146957152 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69719494 | CTTACACATGGGAGC[A/G]CACATGTTCCACTTA | 57626 |
rs146958955 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785583 | AAATTGACACCCTAA[C/G]ATCACAATTAAAAAC | 57626 |
rs146960012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856685 | CTGTAATCTTACATA[A/G]TAAATACTTAGTGCA | 57626 |
rs146973437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061557 | GCTGTGCCTGAGTTA[A/G]TAGCCTTAAGTCAGA | 57626 |
rs146975224 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992441 | AACCACCTGAATTTG[C/T]ATACAGATTGTATAA | 57626 |
rs146978673 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953672 | AAGGTAGCAAAATTA[C/T]AAGCTAGTTGTTTAA | 57626 |
rs146978771 | in-del | -/ATATTAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100169 | TCTTCTGATCTATGA[-/ATATTAT]ATATTATATATTCAT | 57626 |
rs146993521 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890941 | ATATTATTCAAATTA[C/T]ACAACGAAGAAAAGT | 57626 |
rs147005335 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990015 | AGAGGAGATTTGAGG[C/T]CTATATTCAACATTC | 57626 |
rs147016553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059632 | ATTTGCAAATTATCC[A/G]TATTAGTCCATTCTC | 57626 |
rs147026557 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768294 | TCTTCTAAGAGACTA[C/T]AGAATCTGTGAAATA | 57626 |
rs147049584 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911476 | GCTATTAGGGGTTAT[A/G]TTAATGGATTCTCTT | 57626 |
rs147049930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868463 | AAGAGGCTCAGTAAA[C/T]AACAATTATGTAATT | 57626 |
rs147055324 | in-del | -/TG | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929294 | GAATTGAAATTATTC[-/TG]TGTTTTATCTCATTT | 57626 |
rs147059378 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797034 | GCCAAAGCAGGGTAC[A/C]AATTAGGATGTGAAA | 57626 |
rs147066265 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69872217 | GTGCATAGATCACAT[A/G]GTAAGAGAGGAAGCA | 57626 |
rs147077685 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080007 | TCTTGATCCAATCTC[G/T]GGCTCAGTAGGTAAA | 57626 |
rs147089184 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973406 | CAAGTGCTAATAATG[A/T]TAGCTAGCAATGCTT | 57626 |
rs147096816 | in-del | -/ACACT | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889294 | TGACTGAACTGTTGA[-/ACACT]ACCTTAGAATTTCAA | 57626 |
rs147098299 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906866 | AAAAATATAGTTTCA[A/G]TTTTAGGTTACATTA | 57626 |
rs147103216 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69873293 | CATAAATAATTTTCC[-/C]AATTATCTTTTCTAA | 57626 |
rs147108688 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001559 | ACATTTAAACATTGG[A/G]ATATCTATCTATGAT | 57626 |
rs147109036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756423 | TATGGTCATCATTAA[C/T]AAAAAACTTTGCCCT | 57626 |
rs147127242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031448 | AGAGGTTAACAGTTA[C/T]TCAAAATTTACATTA | 57626 |
rs147127525 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078065 | ATCTTTTTTCTTTTT[A/C]TTTTTTATTTTTTCT | 57626 |
rs147137581 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966907 | CTTAAGAAAATGACC[C/T]CTAAGTCCATCCATG | 57626 |
rs147140699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934484 | GTGAGTGGGTGTATA[C/T]GCCTCTAGGGTATAC | 57626 |
rs147150335 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034708 | GAGGAAGAGGGAAAG[A/T]CGCAATCATTTAGGA | 57626 |
rs147152417 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969434 | AAATTAGTGTCAGAT[A/G]GTGAGTTTTATCAAA | 57626 |
rs147178398 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709220 | ATAGATGCAGACATA[C/T]ATAGACACACACACC | 57626 |
rs147186885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923581 | TTACTACTATGTTAT[A/C]TTTGAGGTGATTTTA | 57626 |
rs147221614 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744986 | GATGTAAAATTTCTG[A/G]GTCATAGAATATACT | 57626 |
rs147223049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854490 | AACACATCCCACATT[G/T]GTTACCATGAAGTTT | 57626 |
rs147234121 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983681 | CTATGACAGGAGGGT[C/G]GCTTGAGCCCAGGAG | 57626 |
rs147241529 | in-del | -/TAGAG | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718521 | TTTAAAGTTATTTGT[-/TAGAG]TAGAGTTACTTATAC | 57626 |
rs147253039 | in-del | -/TTTGT | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789844 | AGATTTTGTTTTGTA[-/TTTGT]TTTGTTTTGCATTGT | 57626 |
rs147257428 | snp | A/G | 0.264084 | 0.249603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985934 | TATGTAAATATATAT[A/G]TATTATTTAAAGTAA | 57626 |
rs147259329 | in-del | -/AT | 0.317451 | 0.240729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985776 | ACAAAAATGTGATCC[-/AT]ATATATATATATATA | 57626 |
rs147264694 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088021 | GCAAATCACCATGGC[A/G]CATGTTTATCTATGT | 57626 |
rs147267623 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724087 | TGATCCATCTGCCTC[A/G]GCCTCCCAAAGTGCT | 57626 |
rs147275310 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091428 | TCTACATAACTCATG[A/T]GTTGTTCTCTCAGCA | 57626 |
rs147284489 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728667 | AAAAAAAAAAGCAAA[A/G]TGTGGTGACGTATGC | 57626 |
rs147291413 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766288 | TCATAAACTACAAGA[A/G]TTGTTTTTCATTATT | 57626 |
rs147307929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828192 | AGCACACTCCATGAA[C/G]AGCTAGAAAACTGTG | 57626 |
rs147314978 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866033 | AATAGATGAATAGTA[C/T]AAGTGACTACTCATT | 57626 |
rs147322205 | snp | C/T | 7.2763e-05 | 0.00603127 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107612 | CCCCCGCCGGGCCGC[C/T]GGTGGAAGGAGACGG | 57626 |
rs147327638 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763672 | CACCTAGGTGAGAAC[A/C/G]TGACCAAAAATGTGG | 57626 |
rs147331638 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869538 | TGAATATTATTAAAG[C/T]AAAAACTTTTATTTT | 57626 |
rs147340871 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040704 | ATTTTGGGGGGGTTA[C/T]TTTGTTTTAGATTCA | 57626 |
rs147340911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995704 | CTAAAATGCCACAAT[A/G]TCCAGCAGCAGAGAC | 57626 |
rs147347540 | in-del | -/ATATATATGTATATATATATATGTATATATATATATATAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780694 | TTTCTTCATATATAT[lengthTooLong]ATATATATATACATA | 57626 |
rs147348570 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937983 | GTTAATTCTATCCCA[A/C]GTGTAGTAGAAAAAA | 57626 |
rs147365116 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941705 | AAGATAAACAAAATT[C/G]TTAGATCATTAGTGA | 57626 |
rs147371829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103347 | ATTCAGAACCAGGTA[A/G]TCCATGGTACAGATT | 57626 |
rs147379497 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747790 | TTATATATTGCTGAT[G/T]AATTGAAACTTAGGA | 57626 |
rs147383274 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036550 | ATATGAAATGTTTTA[C/T]TCAGTTTTGCTTATT | 57626 |
rs147390363 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791846 | AGACAACACAGGCAT[-/A]AAATCTTCATGAACA | 57626 |
rs147412449 | snp | A/G | 0.000798881 | 0.01997 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782107 | GCCAAATAAATTTGT[A/G]TTCTTTTTCTGTTTT | 57626 |
rs147414757 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850313 | TTTAAGCTACTTCAA[A/G]CTTTTTTTTGAGAAT | 57626 |
rs147419976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882588 | GTAGTCAATATCCTT[C/T]GTTCTTATTATAACA | 57626 |
rs147422877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951583 | TGCCCAGATTGGGAG[G/T]TCTACCATCCTACCC | 57626 |
rs147435655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779046 | CTCATGATCAGCCCA[C/T]CTCAGCCTCCCAAAG | 57626 |
rs147437541 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886925 | GATTTCAATGCACCA[C/G]AGGATATAGAATTTA | 57626 |
rs147438182 | snp | A/C | 0.461037 | 0.134028 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786026 | ATCAACAGCTTACCC[A/C]CCAAAAAGAGTCCAG | 57626 |
rs147444690 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060209 | ATCATAAGAGAAATA[A/T]TGAGACATCATCTCT | 57626 |
rs147445399 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013700 | CTATAAAATATTTGA[C/G]AGCTGTTCAAAAACA | 57626 |
rs147451577 | in-del | -/TTTG | 0.0178098 | 0.0926698 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041961 | TTGCTTGCTTATTTC[-/TTTG]TTTGTTTCCTGTTGT | 57626 |
rs147454050 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951752 | ACCTTGCTGCTACCA[C/T]TATGGGTCATTTTTA | 57626 |
rs147457572 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915481 | AAACCTGACAAAAAC[A/G]AGAAATGGGGAAACG | 57626 |
rs147457597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954511 | AAACAGATTGTTTAA[A/G]GAAGTAAAGTTGATT | 57626 |
rs147467507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017704 | CATAAGCTCACTACT[A/G]TCACGAGCACAAAAT | 57626 |
rs147480557 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762977 | AACATTTGTCCACTC[C/T]TCTTAACCTACATCA | 57626 |
rs147481435 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70073832 | AGCAAACATAATTTT[-/C]TTTTTTTTTTGAGAT | 57626 |
rs147483570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765798 | ACCCTCCGATCTGTT[A/G]CTAAACAGAGAAGGA | 57626 |
rs147523527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829105 | TCTTGAAAGTTCCAC[A/C]TCCTGGCTGGAGGCC | 57626 |
rs147526477 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899275 | GGTTGTGCAAGCTTC[A/C]CTGAAGTGTGCACAA | 57626 |
rs147539282 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724517 | GCATTGCCCTAATAC[A/C]AAAGCCAGACAAAGA | 57626 |
rs147540937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789423 | TATGACTATTGAGTC[A/G]AGGAATCTGAGATTA | 57626 |
rs147542453 | in-del | -/GT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027182 | CTGTATTTGTGGCTG[-/GT]TTTTTAAAAGTATAA | 57626 |
rs147542460 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69902500 | TTAAAATAATTTTGG[A/G]GAACTACAGTACTGA | 57626 |
rs147556946 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859384 | TAAGCAGAAGGTCAG[A/G]GGGTGAGAGGAGAGG | 57626 |
rs147559851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931375 | ATCACACAATTTTAA[C/T]TGAGCTGAAGTTTCC | 57626 |
rs147570972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756562 | TAATAATCACTAAAT[C/T]CAGAAAGATTTTAGT | 57626 |
rs147573029 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817938 | AACCCTCTATTAAGA[C/G]GCAAAATATAGCTAT | 57626 |
rs147574447 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862648 | TTAACCTCAAGGTGA[A/G]TGTTTTTAGAGAAAG | 57626 |
rs147593232 | snp | C/T | 0.00513366 | 0.0504031 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107321 | CTGGCACCACCTCCT[C/T]CTCTAGTGACTCCAC | 57626 |
rs147614619 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994279 | GTAGGAGTGGAGCTC[C/T]GAGACTTGGAGACAA | 57626 |
rs147618628 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959098 | GTATTGGAGCACAGG[C/T]CAAAGTGGCAGTGGC | 57626 |
rs147628596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803464 | TGCAATTAATATATG[C/T]AGTGGGTAGAATTTA | 57626 |
rs147631645 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101382 | CCTTTCTTACAAGTA[C/G]TTCTGGAGTTTTGGG | 57626 |
rs147641495 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103743 | TGCACAAACTAATTC[A/G]TAGAAAGCTATTCTC | 57626 |
rs147641686 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061709 | ATCTCAATTCTCTTC[C/T]CTCCACTCCAGGTTC | 57626 |
rs147662780 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875254 | TAATAATTATAAAAA[A/T]TAACTACATATTATG | 57626 |
rs147674605 | in-del | -/A | 0.031825 | 0.122064 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960808 | AACATAGTAGATCAG[-/A]AAAAAAAAACTTGAA | 57626 |
rs147676049 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771860 | GAATCAAAATGTGGA[C/G]ACATGACTTCAAAAT | 57626 |
rs147686144 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916655 | AAATGATGAGTTAGT[C/T]GGTGCAGCACACCAG | 57626 |
rs147699030 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980231 | AGTTACTTCCTCAAG[G/T]AAATATTTACTTCTG | 57626 |
rs147699115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804146 | AACCAGAAGATATTA[C/T]ATATAATACAAATAC | 57626 |
rs147711614 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721250 | TTAACCTACCTATGA[C/G]CTGGAAGCCCCCTCC | 57626 |
rs147716869 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083360 | CTTCTTTTTTAGAGA[C/T]AGAGTCTTGCTATGT | 57626 |
rs147718291 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010667 | AGGCCAATGTGGTTG[G/T]ATCACCTGAGGTCAG | 57626 |
rs147728219 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977244 | TGCTACAGATATGTT[A/C]GAATATATGGATCAC | 57626 |
rs147728323 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015142 | TGCCACTAAATGATG[A/G]GGATATGTTCAAAGA | 57626 |
rs147734765 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821504 | ATTTTTAGTAGAAAT[A/G]GGGTTTCATCATGTT | 57626 |
rs147743831 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759259 | ACGTAAGCTCACAGT[A/G]AGATGTGTGCAAGGC | 57626 |
rs147746158 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080149 | AGTCTGAAAGGATAC[A/G]TGTTGGCATGAATCT | 57626 |
rs147747773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718435 | TTCATTTTGAGTACC[A/G]GAGTGGTAATATCAT | 57626 |
rs147768022 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893978 | ATGTTTGCTAATAAA[A/C]ATCAACTGGAAAATG | 57626 |
rs147778191 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718889 | TTATGTTAAAAATGG[C/T]ATGTCATAAAAGAAC | 57626 |
rs147781664 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827093 | GTTACGTTAGATTTT[A/G]AAAACATGTTATTAA | 57626 |
rs147802719 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994010 | ATGCTTTAGCAACAA[C/T]GGAAGTTATAAAGAG | 57626 |
rs147820450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100647 | ACAGGATTTTTGCTT[A/G]TATTTATATTTCAAG | 57626 |
rs147826809 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931899 | GATGCATCTTGTTAT[G/T]CATTTGTTTCTTATT | 57626 |
rs147832071 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739321 | CTATACAGACCAGTG[A/G]CACTATGAAGCTACT | 57626 |
rs147849204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775203 | TCCTGCCTAAACATA[C/T]GATGCATTGGAAAGT | 57626 |
rs147862951 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097096 | ATCATGGCTCAGTTC[A/T]GGGGTAATTAGCATA | 57626 |
rs147871670 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842570 | TGAGGAGAAAATGAA[A/T]CTTACATAGTGTTTG | 57626 |
rs147872291 | in-del | -/AAAT | 0.0876345 | 0.190099 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902909 | TTAAAGTATAATAAA[-/AAAT]AAATAAATAGATAAT | 57626 |
rs147873018 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911266 | ATATAATTTTTAGTA[G/T]GTCTAGTTAAACAGT | 57626 |
rs147886766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737267 | TCATGGTGGCTGCTC[A/G]GGCAGGCAGCTGCTG | 57626 |
rs147886948 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799921 | AAATTCTCATAGGAG[C/T]GCAAACCCTATTGTG | 57626 |
rs147888102 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69846798 | AATCCTGTGTGCACA[C/T]TCTTCAAATTGCAGC | 57626 |
rs147896498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905701 | TAATTCAGTGAACAA[G/T]AATATCATTATTTCC | 57626 |
rs147896645 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949662 | TAACTGGCATAAATA[A/C]TTTTGAATTCTTCTA | 57626 |
rs147928403 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046017 | TTTTTTGTAATTTAT[G/T]TATCTACTCTCTTTC | 57626 |
rs147933502 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947349 | AAAAGTATATTACTA[C/T]ATTTCTTTATATGTG | 57626 |
rs147937802 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005382 | TTGTCCAACCTGCAG[C/T]CTGCAAGCCACATGC | 57626 |
rs147938290 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70051510 | CACCATAAAGAAGTG[C/T]GTGGATATTTCCTAT | 57626 |
rs147944783 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787253 | CATGCTACCTGACTT[C/T]AAACTATACTACAAG | 57626 |
rs147948286 | in-del | -/C | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863434 | GCTTCTCATTTTTTT[-/C]CTCCTAGGAGAATTT | 57626 |
rs147953716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765079 | GCCTTAAACTCCTGA[A/G]TACCTGGGATTGTAG | 57626 |
rs147975132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778241 | AGTTATATAATCTAC[A/G]ATGTCCTTGGGCTAA | 57626 |
rs147989534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981235 | ATACTAAAATTACAC[C/T]AAATATAGTAAATAA | 57626 |
rs147995833 | snp | A/G | 0.000965488 | 0.0219502 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719614 | AAAATGTGATTTAAT[A/G]TCATAGTCTGGATGA | 57626 |
rs147997475 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080738 | AGTAGCTGGGACTAC[A/T]CATGCGCACCACCAC | 57626 |
rs148014946 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882061 | AGTGATATTATCATA[A/C]TCTTACAAGTGGCCA | 57626 |
rs148020118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040823 | GGAAAACTTTTTAAG[C/T]CTTACCCCCATTTTC | 57626 |
rs148022041 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70096074 | CATATATGTACCATA[-/T]TTTTTTATCCATTTG | 57626 |
rs148029982 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092589 | TAGCACTTGATATTA[C/T]AATGATTCGTAGAAT | 57626 |
rs148031436 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022088 | TTTTCTCCTTTTTTC[C/T]TCTAGGAGATTTCAA | 57626 |
rs148037550 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923554 | TGCCATCTTGAATTA[A/G]AATGATTATTATTAC | 57626 |
rs148049156 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086448 | ATTAGCCTGGCGGTG[G/T]TGGGCACCTGTAATC | 57626 |
rs148082358 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832211 | TACTCTATAAACTCA[C/T]GCAAAAAGCTCCTAG | 57626 |
rs148084612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901923 | CTGCCTCAGCCTTCC[A/G]AGCAGCTGGGGTTAC | 57626 |
rs148084771 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993095 | CATATATAATTTTTC[A/G]ATCTTATATTGAATG | 57626 |
rs148089642 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69891552 | TTTTTAATAAAAAAG[G/T]AATGATATTCTAATT | 57626 |
rs148092444 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957726 | ATACCAATTATAAAA[C/T]GGCACTACTTTATAA | 57626 |
rs148092879 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090666 | GAAGATCTGAAACTT[A/T]CTATTTTCTCCCAAG | 57626 |
rs148099657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791719 | GAAGCAAGGACAGCA[C/T]GCAAAAGAATGAAGT | 57626 |
rs148126504 | in-del | -/TC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69849489 | CATTTATGCTCTCTT[-/TC]TCTCTCTCTCTATCT | 57626 |
rs148127683 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937278 | CAGAGAATTGCATTA[A/G]TAAAATAAATTTAAA | 57626 |
rs148135064 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773427 | ACTTCCTATATTTTT[C/T]CTCTATGAGATATAA | 57626 |
rs148136660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839767 | CAATAGACCAATAGA[C/G]TGAGACCAGTAGTTT | 57626 |
rs148137110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995223 | TATTATTTACTATCT[C/G]GTATTTTACCCAGAA | 57626 |
rs148150977 | in-del | -/AAC | 0.265453 | 0.249522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985130 | ACAGACAAACAAGCA[-/AAC]AACAACAACAACAAA | 57626 |
rs148151066 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734300 | TTTCCTGAGGCCTCC[C/T]TAGAAGCTGTGCAGA | 57626 |
rs148160013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877053 | AAAAAAAAAAGATAT[A/G]AACACTACCAATTCT | 57626 |
rs148167047 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034676 | TGTGTAGAGGGGAAG[A/G]GGTGCATGTGTATTT | 57626 |
rs148170667 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746769 | AAGGCTCACACAAAT[G/T]AGAGACCACAGTCAC | 57626 |
rs148178124 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104690 | TCATTGTTTGGTGAT[A/G]TGATAATGACCTAAG | 57626 |
rs148188393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743452 | GGAGTCTTGCTGTTG[G/T]AATTTACTAATAGAA | 57626 |
rs148207075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757318 | TCATTATTTCTGTGG[A/C]CAAAATAATTTAACA | 57626 |
rs148210672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044171 | CTTCTCACAGCCCAG[C/T]TCATACTGGCCTTTT | 57626 |
rs148212164 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69850066 | TTCAGTCACATTCGA[C/T]AGCAAAAATCCATTA | 57626 |
rs148213516 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016614 | CTGAATTTTGGGCAC[C/T]GATGAGGATCGAAGG | 57626 |
rs148242521 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058942 | TATTATCAAAGGTGC[C/T]GATAATATACAATGG | 57626 |
rs148251264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953242 | TCAATGACAATTCTC[C/T]ATTTGGGTATCATCT | 57626 |
rs148265684 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854898 | GTTTTTCATCTCTCA[A/G]GTACCTATTTTTGAA | 57626 |
rs148287010 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961787 | TATCGTGAATTTGAA[C/T]GCATAACATATATTG | 57626 |
rs148295240 | snp | G/T | 0.183886 | 0.241099 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867964 | ATATGTAACTAACCT[G/T]CACGTTGTGCACATG | 57626 |
rs148295415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025928 | AATAAAGCAGCAATC[A/C]CCAAAGCATTGACTC | 57626 |
rs148297855 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940545 | AAAAATAAGGTTCAG[A/G]ATATATGCCTACAAA | 57626 |
rs148301182 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857697 | GTATTTCAGGGTTAA[A/C]TTTAAGGTAAATCAT | 57626 |
rs148303113 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927979 | AGGATTAACAAGAAT[A/G]CTGGACAGAAATATA | 57626 |
rs148309077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765731 | CAGAGCAGAGGTATA[C/T]TTTGGAATGCTGTGC | 57626 |
rs148311375 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827698 | ATCGTGCCACTGCAC[C/T]CCAGCCTGGCGACAG | 57626 |
rs148328125 | in-del | -/TA | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877680 | CCTTTTTCTCTGGTC[-/TA]TAGCAAAGTAAATAA | 57626 |
rs148339773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966326 | TCCTAGGGCTCTTAA[A/G]AATTACGCTAATTCT | 57626 |
rs148345171 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801435 | GAGTGGTTATATCCA[C/T]ATTGTTTTTTCTCTT | 57626 |
rs148347992 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872793 | CAAGGCTCTTTTTAA[C/T]AACCGGCTCTTGTGT | 57626 |
rs148350198 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899148 | ATGAGGCACAAAATT[A/T]ATTGGATATCTTTGA | 57626 |
rs148361092 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769777 | GAGCTATTCTGTCAC[A/T]CAGTAAAATTCTTCC | 57626 |
rs148367063 | snp | A/G | 7.28695e-05 | 0.00603568 | utr-variant-5-prime, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107715 | GCTTTACGCACAGAA[A/G]GCAAAAGGCTGGCAG | 57626 |
rs148380950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706969 | CTCTAACTACAGTGT[A/G]TATGTAAGGCATAAT | 57626 |
rs148383881 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912834 | CCCCATGCTGCTTGA[A/G]TCCTGCTGGGAGACT | 57626 |
rs148389449 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074549 | ACACAGGTATTAGAT[A/G]CAAAAAAGAGATCCT | 57626 |
rs148391314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941815 | GAAACACAAAGGATC[A/G]TTCAAGGCTGCTATG | 57626 |
rs148396752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029384 | CTCCAACTTGATGAA[G/T]GTGAAGCCTGATATT | 57626 |
rs148403969 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766575 | TTCAGAAATATGAAT[G/T]GAAAAGAAGGTGGGA | 57626 |
rs148404592 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829222 | TCCCCTACTACCTCC[A/G]CTGTTGTGTATGGCT | 57626 |
rs148408767 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70057783 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAAGA | 57626 |
rs148431106 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974246 | TTGATAATAATGTAT[C/T]TAGTTTAATATATTC | 57626 |
rs148435377 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701501 | CTAACATATGGCCAG[A/G]CATTTTTCCTGTATA | 57626 |
rs148446732 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967485 | TCAAATTTGAATGGA[C/T]GAAGAGTTGCTTCTA | 57626 |
rs148454876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874038 | TTCTAGGCAATCTCA[A/G]TTGAGGGGTGGAGTG | 57626 |
rs148461728 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032819 | CTTTTCAAATGTCAT[A/G]ATTGAAATTTTAGAT | 57626 |
rs148471010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754576 | CTTTTTAAGAACAGG[A/G]CCTGTGTTTTACACT | 57626 |
rs148472799 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012860 | GTGAGGTGAGATCTC[A/G]CCCCTGCACTCCAGC | 57626 |
rs148474792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815277 | ACTGCAGCACTATTC[A/G]CAATAGCAAAGACAT | 57626 |
rs148479515 | in-del | -/TGTG | 0.376394 | 0.215696 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751113 | CATGTCATGTGTGTA[-/TGTG]TGTGTGTGTGTGTGT | 57626 |
rs148482917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979280 | CTTCTCTTCAAGGTC[A/G]TTAATCTTTCAGATA | 57626 |
rs148486798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710594 | CAAAATGATGACTTT[A/G]AATTGATTTTTCTAT | 57626 |
rs148491170 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075681 | TGTGTGTATATATAT[A/G]TACACACACGTGTGT | 57626 |
rs148491276 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914955 | AAATACACATGTAAA[C/G]AACACTAACATATCA | 57626 |
rs148507765 | snp | A/C/T | 0.00756178 | 0.0610554 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846927 | TATAAAAATAGGATG[A/C/T]ATCATTCAAGTATCT | 57626 |
rs148521552 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082673 | ACCTGGGCATATTAC[A/G]TGATGCTGAAGTTTG | 57626 |
rs148523432 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720973 | AAATCCTGGGACTCC[A/C]AAATCACTAAAGCCA | 57626 |
rs148525857 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987722 | CTCTTTGAAATTTAT[A/G]TGAATGACTCTTAGA | 57626 |
rs148526977 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786627 | tctctcaccactcct[A/G]ttcaacatactgttg | 57626 |
rs148554070 | snp | C/T | 0.396 | 0.202938 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782432 | GAAAGGGGTGACAGA[C/T]GGCACCTGGAAAATC | 57626 |
rs148562397 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825863 | GAAATATTGCTGATA[A/G]GGTATATCCCAGATA | 57626 |
rs148563457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896099 | TTTTTCTTGGTGGCC[A/G]TTGCCTGGAGGTCAC | 57626 |
rs148564977 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095379 | GGAACCTATTGGAAA[A/G]TAAAATTACATGGAA | 57626 |
rs148577475 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724557 | AAACAAACAAACAAA[C/G]AAAAACTAGAGGCTA | 57626 |
rs148579492 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931096 | TTTATAAAATGATAA[G/T]TCACTTACTCTCTTT | 57626 |
rs148588338 | snp | A/G | 0.0014023 | 0.0264421 | intron-variant, synonymous-codon, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975762 | AGCTACTGGAGTCCA[A/G]ATCACTTTGAGGTGT | 57626 |
rs148606950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993987 | GTCATTAACTAGATG[C/T]TTAAAAAATGCTTTA | 57626 |
rs148618122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064570 | CATGGTTGTAATGTT[G/T]CATGTTTTCCATTTT | 57626 |
rs148647559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103123 | GGGAAAGGTACAGCA[C/T]GTTTATGCATGACAT | 57626 |
rs148648253 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945154 | CCACGCCCAGCTAAT[A/T]TTTTGTATGTTTAGA | 57626 |
rs148676095 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736401 | AAAAACAGATTTTGG[C/G]ATGGATGTGGTGAAA | 57626 |
rs148676834 | in-del | -/T | 0.0579587 | 0.160063 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877473 | AACTATATATATATA[-/T]TTTTTTTTTCAGTCA | 57626 |
rs148680281 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050247 | CTGGCTGTGTTACAT[A/G]AAATAGTTACATATT | 57626 |
rs148699449 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106734 | GTGGCCTCATTTTGT[C/T]CACCTCATTACTCCT | 57626 |
rs148701677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037071 | GTATAACCTTAGGGT[A/T]TTTTCACTACATATT | 57626 |
rs148701801 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949302 | TAGGCAACTCTAGGC[C/T]GCGGAAGTTTTCAGA | 57626 |
rs148716485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809546 | TCGGCTCTATGAGAG[A/G]TGCTTAAGGGAATTT | 57626 |
rs148737781 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955418 | TTCAATATGATTAAA[A/G]GTCTGCCATTTGGCA | 57626 |
rs148744509 | in-del | -/AT | 0.0729998 | 0.176553 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730266 | TGTACTAACACTTTA[-/AT]ATGTGTGTGTGTGTG | 57626 |
rs148752764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851626 | TTAGAATAAAAGATA[C/T]TAATAGACATTGGTA | 57626 |
rs148754161 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921845 | GGTTATACAAAAGCA[C/T]AGTAATAATAAGCTT | 57626 |
rs148764606 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060450 | AATCAATATTTTAAA[A/G]ACACACCTGCCCTCC | 57626 |
rs148765113 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69728137 | GTAAACAGCAATTTC[-/T]TTTTTTTTCTTTCTT | 57626 |
rs148771762 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789061 | TCTATCTATCTATCT[A/G]TCTACTTATTTACCT | 57626 |
rs148812789 | in-del | -/TA | 0.399968 | 0.200024 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798093 | AAGCTCCCAAATGTT[-/TA]TATAAGATAATATAA | 57626 |
rs148819317 | snp | A/G | 0.000132037 | 0.00812411 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69719395 | ATCCAGTAGCCGGGA[A/G]CAGTGATTTGAAGCA | 57626 |
rs148820822 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086598 | AAAAAAAAAAAGAAA[A/G]AAAGAAAGAAAGAAA | 57626 |
rs148842848 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69759862 | GTTAAGACAAGATTG[C/T]CAGGCAAAGCACCTG | 57626 |
rs148844852 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935461 | ATATATTATAAAGCC[A/G]GGAACTAAACAAGGA | 57626 |
rs148847336 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69957182 | GAGCTGCATTAGGTA[C/T]AGGAAAATGCTCACG | 57626 |
rs148850862 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923428 | AGGTGCTAAAGTTCT[C/T]GTCTTCTTGAAATTG | 57626 |
rs148855155 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69733231 | ACACATATGAAAGAT[-/A]AAAAAAAAATCACTG | 57626 |
rs148858864 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822800 | AATATAGAATAACTG[G/T]TTTAATATAATTATC | 57626 |
rs148881417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061494 | GTGTGGGCAGCATAT[C/T]GTGCTCACTCTCTTT | 57626 |
rs148881791 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864454 | TGAAACTTAAATATG[A/C]CAAAATGATGAAATT | 57626 |
rs148900510 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960635 | TGGTCTGTGAGCTTC[A/G]TGAGGGCAATACACA | 57626 |
rs148901016 | in-del | -/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69940792 | ATTTTATCTTAAAGG[-/CA]AAAAAAAAAAAAAAA | 57626 |
rs148912820 | snp | A/G | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107380 | GTGCCCTGCCCAGGA[A/G]CCCCTTGCTGCAGCC | 57626 |
rs148918039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872053 | TGTTGCTATAAAGGA[C/T]TACCTGAGGCTAGAT | 57626 |
rs148919958 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944004 | TATAATTTATGCAGA[A/G]AAGAATGAGCACAGC | 57626 |
rs148927384 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779657 | ACACATATGTCTATA[G/T]CTTTATCAAATCTGC | 57626 |
rs148930007 | snp | C/T | 0.00894477 | 0.066275 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740360 | CCAATAACTTTTTTT[C/T]TAAGATTAAAAAATA | 57626 |
rs148930669 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767606 | CCAATCCTTAAATTA[A/T]AATTAATTTTGCAGA | 57626 |
rs148930838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101417 | TGAAAATCCAATTCA[A/G]TAGCCGTATATATAT | 57626 |
rs148934532 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831349 | CTAGAAAAGCTAGCA[C/G]ATTTGGATAAATTCC | 57626 |
rs148965564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042295 | TGTGTCTGTGTGTGC[A/G]TGCTTGTGTGGGTGT | 57626 |
rs148967426 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977039 | TATCAGTGAAAATCT[C/G]TGATTTCATTAAGCT | 57626 |
rs148969501 | in-del | -/TATAT | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774369 | CTTGTTAAACTTTAA[-/TATAT]TATATTTTTGTATAT | 57626 |
rs148977362 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714180 | TTCAATGCAAAAAAA[A/C]TTTTAAAGTTAATTT | 57626 |
rs148979296 | snp | G/T | 0.460925 | 0.134204 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786706 | CAATTAGGAAAAGAG[G/T]AAGTCAAATTGTCCC | 57626 |
rs149006716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089261 | AATACTTGGGCAACA[C/T]TAGTTTCACTGTTGT | 57626 |
rs149014058 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816589 | TATATGTAACTACCT[A/G]TTTTAAATGTTCTAC | 57626 |
rs149017565 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889216 | CTCAGGGTTTAAAAC[A/G]AATTTTACTGGGCTT | 57626 |
rs149019425 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917457 | ATTAAGAAAACCCCC[A/G]TCCCAGTGAGCACAT | 57626 |
rs149024734 | in-del | -/TC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69823819 | ATCATTGAAATTTTT[-/TC]TCTCTCTCTCTCTTA | 57626 |
rs149048279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989317 | TCCATTGGTCTATGC[A/G]TCTCTTTTTGTACTA | 57626 |
rs149052477 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722450 | TATCTATCTAATCTA[G/T]TATCAAACTACATAT | 57626 |
rs149056840 | in-del | -/AAATA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69815018 | CGTCTCTAAAAAAAT[-/AAATA]AAATAAAATAAAATA | 57626 |
rs149058715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058574 | TAAAGAAATTGAGGA[C/T]GTCCAATATGGAAAA | 57626 |
rs149060459 | snp | A/C | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952996 | ATGGTTATTATTTAA[A/C]AACATTTAGGAAATT | 57626 |
rs149065956 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787621 | ACTTCATGTCTAAAA[C/T]ACCAAAAGCAATGGC | 57626 |
rs149071106 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886450 | ATTCATTTCTTCTGT[A/G]CATTAATTAAATTAT | 57626 |
rs149075661 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939536 | TATAAAAGGGCAGCT[A/G]TGGAAGTGAATGTAC | 57626 |
rs149088257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096766 | GACACTATTCTGTGA[C/T]TGTTTCCAGATAGTC | 57626 |
rs149090603 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827567 | AAACCCCGTCTCTAC[A/G]GAAAATACGAAAATT | 57626 |
rs149091868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897606 | TGTCACTAAATGCCC[A/C]CTTCCTCCAGAGTGC | 57626 |
rs149099982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992822 | TCACAAAATAAGATA[C/T]AAAATGAATTACTTA | 57626 |
rs149104460 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728122 | GAGATTCAGTAAACA[A/G]CAATTTCTTTTTTTT | 57626 |
rs149128390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905164 | GTCATAAATCTTCAA[G/T]CAATGGTTTTGCCTA | 57626 |
rs149133158 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971852 | GGCATAGGCCAATGC[C/T]AGAGTATGTTTGATA | 57626 |
rs149134101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746283 | TCAATATAATTACTA[C/T]ACATTTTAGTTCTCT | 57626 |
rs149142516 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067010 | CAAGCACTTTGTAAG[C/T]TCTAGGCACTCACTA | 57626 |
rs149143295 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795984 | TTTCACTCAACCCAC[A/G]TTAACTATTTTTCCC | 57626 |
rs149176551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005011 | TGTCATAATTGTAAC[A/G]TAAGTCCTAGTTTTG | 57626 |
rs149179434 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843469 | TTAAAACGAGTTTCT[A/G]TGCTATCCCTAGTAT | 57626 |
rs149181651 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912637 | GTGCAACTATATTGG[C/G]AGGTAGCAGGTGGCT | 57626 |
rs149189303 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752443 | TTGTTAATTATATTA[A/C]TATGTATCATGAAAA | 57626 |
rs149198898 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789286 | TGTCTGTCTGTCTTT[C/T]ATTTTGTATGGGTAA | 57626 |
rs149205261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053000 | AGTACACAATTGCCA[A/G]ACATCCAAACAAGGC | 57626 |
rs149218714 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950217 | TCGTTCTATTTCTGT[A/C]CACCTTATACCTATA | 57626 |
rs149225965 | snp | A/T | 0.127254 | 0.217792 | intron-variant | KLHL1 | GRCh38.p7 | 13:69784378 | TGCTCCAATTAAAAG[A/T]CACAGACTAGCAAAT | 57626 |
rs149227100 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039790 | AACTATAGGTATGTA[A/C]CATCATGCCTAGCTA | 57626 |
rs149228279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855560 | TGTAATCTTGGGGGC[A/G]GTTTTTCTGCTCATG | 57626 |
rs149229232 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010693 | GTCAGGAGTTTGAGA[A/C]CAGCCTGGCCAATAT | 57626 |
rs149232080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810558 | CAACAAAGTTTATAG[C/T]GCTGAACATCTACAT | 57626 |
rs149237445 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69907539 | TTATATAAATACTTC[A/G]CTAGATATTGAAAGT | 57626 |
rs149237646 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080361 | CATAAATGCAGAAAA[A/G]TGTATGATAATTAGA | 57626 |
rs149248084 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701261 | TAGAAAAACAGTAAA[C/T]CAATCAGATACTGTC | 57626 |
rs149266875 | in-del | -/ACTGGTGAACTTGGTACATAGTTCACCC | 0.398354 | 0.201224 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935207 | TGGTACATAGTTGGT[-/ACTGGTGAACTTGGTACATAGTTCACCC]ACTGGTGAACTTGGT | 57626 |
rs149280246 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007384 | TATATAGGTATATAT[C/T]GATACACATTATTAT | 57626 |
rs149282344 | in-del | -/TGAG | 0.479824 | 0.098392 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960708 | TTAATACTTGTATAT[-/TGAG]TAACATTCAACAAAT | 57626 |
rs149287889 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845683 | TATAACTTATACTAG[C/T]ACTTGCTCTTTGGAA | 57626 |
rs149288516 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109230 | ATCTATACTTAGAAT[G/T]GTGAGGATTGCGATC | 57626 |
rs149290931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914856 | GCTGGCAGCAAAATA[A/G]ATAAAAGATGTAAAC | 57626 |
rs149296098 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754419 | TGTATATACAAATAT[A/C]CGAACTTACCATAAC | 57626 |
rs149315768 | in-del | -/GA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026750 | TGTGTGTGTAAGAGG[-/GA]GAGAGAGAGAGACAG | 57626 |
rs149319587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895677 | GGTTCCTTAATTTTT[A/G]GAATATTTGGGAATA | 57626 |
rs149321569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054287 | TAAACTTTAAATAAT[A/G]CAAATCGAATTTTTA | 57626 |
rs149326975 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951553 | TTGGCAGTTTTAATA[A/G]TTTATCTCACATTCT | 57626 |
rs149331662 | in-del | -/ACTAAAAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69757791 | TGAAATCTCGTCCCT[-/ACTAAAAA]TGCAAAAAATTAGCT | 57626 |
rs149332120 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012195 | CTCTTATTAAATTGT[C/T]TCACAGCATTCTTCA | 57626 |
rs149349964 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720550 | TTACTACTGGGGAAG[G/T]TTCAAAGTGCAAGGG | 57626 |
rs149371409 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865689 | ATTTTAAAGGTGCAT[A/G]TTTTTAAAATTTCTT | 57626 |
rs149373770 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095338 | TTTAGATCCTTAGGA[C/T]TATCAGGAATTGACT | 57626 |
rs149375857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023582 | AGTTCACAAAGTGTC[G/T]ATTTTTTGTTGTATC | 57626 |
rs149385586 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987436 | TTTATTTATATTTTC[A/G]GCTATTCAATAAAAA | 57626 |
rs149388180 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824840 | TGGGTTACATACCTG[C/T]ATGCATTGTGAAAAC | 57626 |
rs149408074 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034047 | TTCCCTAAATAGAGT[A/C]AAAAAATAACACTGC | 57626 |
rs149408210 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772720 | TAGGGTTTGGTTGCA[A/G]TGGTAGCTGTTTTTA | 57626 |
rs149410288 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69968935 | AGAATTATAGTGATG[C/T]TTACATCTATAAGCA | 57626 |
rs149425994 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870442 | AAATTTCAACATGAG[C/T]TTTTGGGGGACAAAC | 57626 |
rs149428819 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028804 | CAATGTGGCGAAACT[G/T]CATCTCTACAGAAAA | 57626 |
rs149446453 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849063 | ATGATTTAATTGCAT[C/G]CGATTTGGGCTCAGC | 57626 |
rs149456457 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781189 | AAGAACTCTGTGAAT[A/G]TACAACAGTTTTTCC | 57626 |
rs149459609 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743312 | GTCAGGTTAGGTGGC[A/G]GTAGGGAGATGATTA | 57626 |
rs149470334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102717 | ATTTCAGTCTTCTTA[C/T]CTATGTAATCATTAT | 57626 |
rs149482256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086101 | AATGGAAATGTACCT[A/G]CAGTGGAATCTCCAC | 57626 |
rs149498660 | snp | C/T | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782941 | GACACCTCACATGGC[C/T]GGGTACTCCTCTGAG | 57626 |
rs149501004 | in-del | -/T | 0.0322114 | 0.122752 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036819 | CCAACTTGGGTTTGA[-/T]TTTTAATGCCATGGT | 57626 |
rs149501319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079135 | AGTTAATACAGAGTC[A/T]CTAAGGCTTCCTGGC | 57626 |
rs149502697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878381 | AGTCTTTCAAATATT[C/G]TTCTCTCACTCACCT | 57626 |
rs149517760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949128 | ATTCGTATGATATAC[A/G]TGTTATATTAATGAA | 57626 |
rs149533130 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932563 | TATTTTAAAATGTTT[A/C]GTATTCCTTCTTGAA | 57626 |
rs149534072 | snp | A/G/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090518 | ATTATTGATTGACAG[A/G/T]TCATTATCCTCTGCT | 57626 |
rs149545474 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69982479 | TAATAATAATAATAA[A/T]AAAATAAAAAGCAAT | 57626 |
rs149546540 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69819807 | TGATAAACAGAGCAA[C/T]GTGATAATAAAATTT | 57626 |
rs149548849 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69891223 | GGACTGAAGTGAATG[G/T]CTGCCAGTTTTCTTT | 57626 |
rs149572898 | in-del | -/AAAACAAAAAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068360 | ACAAAAACAAAAACA[-/AAAACAAAAAC]AAAAAAAAAGGATTT | 57626 |
rs149584845 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898804 | GAGACATTTTTTTCT[A/C/G]TTCAATGCCACATGT | 57626 |
rs149585529 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060409 | TCTAGCAATCCCACT[A/G]CCAGATATGTAACAA | 57626 |
rs149588072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990988 | TCAAAATAGAAATGA[A/C]GGTCAAGAAAATTGC | 57626 |
rs149592301 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955045 | CTTTGAAGGCTCAGT[C/T]TCTTAAATCAAGAAT | 57626 |
rs149595509 | in-del | -/A | 0.0693013 | 0.172766 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853976 | TTCTCATAGATTTAT[-/A]AAACCTATTCCAAAT | 57626 |
rs149599577 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788989 | AGGAGAATTCAGGAG[A/T]AAAAGATAAACACTG | 57626 |
rs149615039 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098558 | TTGAAAAGTTGAGGA[A/T]TAAAGACTTATTTGA | 57626 |
rs149617449 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737739 | AAGAGAACTCTGATA[A/T]CCCTGAGAGGAGCCC | 57626 |
rs149619710 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996839 | GGCCTATGACATTGG[A/T]GAAAGTAAGTATACA | 57626 |
rs149635520 | in-del | -/AGC | 0.0418186 | 0.138422 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755902 | GCCTAATCACTTATT[-/AGC]TGTGGGATTTTGTGA | 57626 |
rs149680471 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967220 | TCCTTTGAGGCATCT[C/G]GCAAAGTAAATTTAA | 57626 |
rs149687648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061209 | ACAGTGTAGAATTCT[C/T]GCACATCTTTTGTTA | 57626 |
rs149689755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992140 | CGAAATCTACTGAAA[C/T]ACTTCATTTTATGAA | 57626 |
rs149691187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900998 | TCTTTGGTTCTGTTC[C/T]AGGGAAAACACACAT | 57626 |
rs149695162 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863525 | TTTGCATTTTTCATG[A/G]TTGGTAAAACCTGGA | 57626 |
rs149698035 | snp | C/T | 0.401747 | 0.198678 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786357 | CTGGTTCAATATACG[C/T]GAATCAATAAATGTA | 57626 |
rs149703865 | in-del | -/C | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862637 | ATGTTGAAGCGTTAA[-/C]CTCAAGGTGAGTGTT | 57626 |
rs149704947 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790732 | TACAGGAAAATCCAA[C/T]ACCCTTTTCATGATA | 57626 |
rs149721597 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998267 | GGCAGAAGATCAAAT[A/G]GTAGTAGAAATATTA | 57626 |
rs149725454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739295 | ACCAGCCGCAACGAA[A/G]ACACACTTAACTATA | 57626 |
rs149742604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837515 | TAGCTATATAATGTC[C/T]GAGAGAGGAAATTGA | 57626 |
rs149744720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905064 | TTTTCTGTAAATTCA[A/G]TTTGCTTCCTACCTC | 57626 |
rs149747256 | in-del | -/TTC | 0.0832709 | 0.186283 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895087 | ACTTCGGATCTTGCT[-/TTC]TTCTTCTTGCTTTTC | 57626 |
rs149762242 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081861 | TGTGGTAATTTGTTA[A/T]GCAGGAATGGAAAAC | 57626 |
rs149763152 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812420 | TAGGCATAGGCAAGG[A/T]CTTCATGTCTAAAAC | 57626 |
rs149764612 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009718 | GTGGAACTAATAGGT[A/G]TATTTCATTGCTATT | 57626 |
rs149764994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882743 | TGAGCTTTGTTATGC[A/C]GGCAGAATGTACTAA | 57626 |
rs149774671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976218 | AATTCTTGAGATGTC[A/G]TAGTAAATGTTGCCT | 57626 |
rs149780007 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910873 | ACACATATATAAGCA[A/G]TCAGGAAATAAGCAA | 57626 |
rs149782982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073223 | CCATAGAATACTATG[C/T]GGCCATAAAAAAGGA | 57626 |
rs149815013 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756364 | TTAGATTTTGTGACT[A/C]AAATGAATTTCTGAT | 57626 |
rs149815442 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816425 | GCCGCCACGCCTGGC[C/T]AATTTTTTTTTTTCC | 57626 |
rs149816943 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015379 | TAAACATATGTATTA[C/T]AGTCTTATGTGACCA | 57626 |
rs149831070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712398 | GACTACAATTTTCCA[C/T]ATGAGATATCCAAAT | 57626 |
rs149831253 | snp | A/G | 1.64855e-05 | 0.00287097 | intron-variant, synonymous-codon, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69975622 | CAGACTACTGTACCT[A/G]TGTGCAGGTATCTTT | 57626 |
rs149833945 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916965 | TGTGTAGGCTATTTT[C/T]GAGTAAAGTATAAGA | 57626 |
rs149838543 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963151 | ATTGCAGCCTTGAAC[A/C]CCAGGGCTCAAAGTG | 57626 |
rs149853152 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858822 | GCCAAGCATGGAAAA[C/G]AGTAAGGCTATTTCA | 57626 |
rs149855483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930627 | ACTTAACTAATAAAG[A/G]CAATATGCCATTGTT | 57626 |
rs149857515 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952374 | ATTTTTTCTTGTAAG[A/T]CTGAATCCCATTACC | 57626 |
rs149898894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096445 | TTCTCTGATGATTAA[C/T]GATGGTGAGCATTTT | 57626 |
rs149899069 | snp | A/G | 0.395818 | 0.203069 | intron-variant | KLHL1 | GRCh38.p7 | 13:69784095 | AACTAAGCCTCATAA[A/G]TGAAGGAGAAATAAA | 57626 |
rs149900403 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841094 | TCATTTGGAACACAC[A/G]TTAGGAATAGCTTAA | 57626 |
rs149900524 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025332 | TGGTGATCTCATTTA[A/G]TTGACTTTGAGGTGG | 57626 |
rs149901873 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866766 | CCCAGGGACAAAGCA[C/T]TGGGAAATGCTTATC | 57626 |
rs149904985 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827474 | TGGTGGCTCACGCCT[A/G]TAATCCCAGCCCTTT | 57626 |
rs149915176 | in-del | -/AATAA/AATAAAATAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70010911 | AAAAATAATAATAAT[-/AATAA/AATAAAATAA]AATAAAATAAAATAA | 57626 |
rs149917339 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764560 | CACAAAGAAAAAATA[C/G]TTTGCATCGCTATCA | 57626 |
rs149932639 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036709 | ATTCCCTTATTTAAA[A/T]TTCCTTGTTTAAATT | 57626 |
rs149934656 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69970031 | GAAAGCTGTGCAGAC[A/T]TCTTATCCCAGCTTA | 57626 |
rs149936131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774691 | ACACACACAAGCAAG[C/T]AGAAATAGCCTATAG | 57626 |
rs149939157 | in-del | -/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981990 | ATAGTGACATAAAAA[-/G]TTTTAAATGTTGGGA | 57626 |
rs149951961 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779079 | CTGGGATTACAGGTC[A/T]AAGCCACCATGCCCG | 57626 |
rs149952625 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799724 | TGCTGCCATGGCTCT[G/T]TTCCTTTCTGGAGGC | 57626 |
rs149955396 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871834 | GGCTTTTCTTGTCTA[C/T]ATTTCTATCAGCATA | 57626 |
rs149974618 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851293 | CATGAGAAACTACTA[A/C/T]GCTTCCTTTAGTTCT | 57626 |
rs149974897 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045446 | TATGGAAAAAATACC[A/G]TCTGTCAGAAAGAGG | 57626 |
rs149975982 | in-del | -/TCTG | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795419 | AATTAAACTCTGTTA[-/TCTG]TCTAACATGTATGTT | 57626 |
rs149984799 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004822 | TAATTAAAATACTAC[C/T]AGCTGAAAACAATGA | 57626 |
rs149985113 | in-del | -/TT | 0.0360663 | 0.129354 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951091 | GATTATGCTTACCTC[-/TT]TGTCTTGTTGACTGA | 57626 |
rs149988760 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745653 | TTAAATATAAAAATT[A/G]AAACAATAAACTTTT | 57626 |
rs149992458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945924 | CTGGAAAGAACTAAA[A/G]TGTTACATGACAGGT | 57626 |
rs149993559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103845 | TGACTGGACTCTATG[A/G]CATCTATCAAAGAGG | 57626 |
rs150010664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887652 | TTTGCCACTTTATAA[C/G]AAGGGTCACTTTTCC | 57626 |
rs150023311 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718198 | TTTCTGCTGTCAGTG[C/T]TATCAGCTAAACATC | 57626 |
rs150025080 | snp | C/G | 0.452719 | 0.146304 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783729 | TGAAAGTGACGGGGA[C/G]AATGGAACCAAGTTG | 57626 |
rs150027292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051876 | TTTTGTTGTGGACTA[C/T]AAGAAAACAATGCTA | 57626 |
rs150029142 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984190 | AAAAGAAATTATTTA[A/G]GCAGATAGTGAGGGT | 57626 |
rs150042655 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029456 | CCAATATTCAACATT[A/C]TTAAAGAAAAGAATT | 57626 |
rs150045626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950011 | ATACAAATTCTACCC[A/G]TGAAATTCTATAATC | 57626 |
rs150056055 | in-del | -/GTTAA | 0.0622301 | 0.165053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823177 | TTGAATCAGCATTTG[-/GTTAA]GTTGTTAACTTACAA | 57626 |
rs150056694 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092179 | GACACAACTCCTTGC[C/T]CATGGAAACAGAAAT | 57626 |
rs150060356 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993940 | CAGAGTAGAGACATG[G/T]AATATAGAGCTGATA | 57626 |
rs150060862 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934466 | TCATTATAAACAAAT[C/T]ATGTGAGTGGGTGTA | 57626 |
rs150063552 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893657 | GATGCTCTAAATACG[A/G]AAGTTGGTACAAAAC | 57626 |
rs150070644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730453 | TAAATGGTAAGAAAA[A/G]GTCACTAAATAACCG | 57626 |
rs150088825 | snp | A/G | 1.65034e-05 | 0.00287253 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69719392 | ATAATCCAGTAGCCG[A/G]GAACAGTGATTTGAA | 57626 |
rs150094659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853545 | CACTTCTGTTCTTTA[C/T]ACATGGCCCTCCTGG | 57626 |
rs150099943 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006921 | TTGCATATGTACAAA[A/T]TATTTTTCATTTTGT | 57626 |
rs150120644 | snp | A/G/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956959 | ACATTGCTACTTCTC[A/G/T]AGGTGATTTGAACAT | 57626 |
rs150128417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053982 | CCTGAATGTGACAGG[A/T]TTTGTGTGGCCTTTG | 57626 |
rs150131296 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985298 | ACAAAGAAAAAACCA[A/G]TCTGAGTGTAAAATA | 57626 |
rs150140694 | snp | C/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107336 | CCTCTAGTGACTCCA[C/T]GTAGAAGAGAGTCCT | 57626 |
rs150154794 | in-del | -/A | 0.100588 | 0.200439 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892606 | ACCCTAACTTCTCAG[-/A]AAAAAAAAACAACAA | 57626 |
rs150163266 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994328 | GCCAAGAAACTTGAA[C/T]TCTTTCCTTAAGCCT | 57626 |
rs150168093 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794731 | TATAATGAATTACCA[A/G]GTAGGGATAGCAAGA | 57626 |
rs150206950 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902103 | CCACGCCCAGCCCAC[A/C]ATGAGTTTTTTTATA | 57626 |
rs150209610 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967982 | TTCCAATTTTGAAAG[A/G/T]AGTTATACCGTGGGT | 57626 |
rs150213278 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741568 | TTGCTGGTTCCCCAC[A/G]CCCCAATTCCCATAG | 57626 |
rs150222167 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792000 | CGTCAGGAGAAATAG[C/T]GAATGCATGCTGGGC | 57626 |
rs150223961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865409 | ACATTTAAAAAGGTT[A/G]TAACTAAGAATAACA | 57626 |
rs150224917 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062696 | TGCCTATATAATCAG[A/G]CTTTTATCTGCTTAC | 57626 |
rs150247513 | in-del | -/ATTG | 0.0244538 | 0.107838 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741307 | AAATATAATGTAAAT[-/ATTG]ATTGATGTGCTCTTT | 57626 |
rs150252379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848280 | TTGTTCACCAAAGCT[C/T]GTAGCACTTCATTAG | 57626 |
rs150255168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077385 | TATTCTATGACTGTC[A/G]CTGTAAGCCATTCTG | 57626 |
rs150264314 | in-del | -/CAC | 0.403039 | 0.197684 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774673 | CTTAATAAAAAAAAA[-/CAC]ACACACACAAGCAAG | 57626 |
rs150267578 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747175 | ATTTGTTTTATTTAG[C/T]TTTTACAGTTATACA | 57626 |
rs150286893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722126 | CACAGCTCTCGTACA[C/T]AGTTTATAAATAAAC | 57626 |
rs150289379 | snp | C/G/T | 0.00358891 | 0.0422285 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814167 | CCCTAATCAATAAAT[C/G/T]GTTTCGGGAACACAG | 57626 |
rs150328568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927313 | AGTCACAAAAGACAA[C/T]ATATGTGGGAATCTT | 57626 |
rs150337455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090254 | AGAATGTGACAAATG[A/C]CAAACTAGTGATCTG | 57626 |
rs150339353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017157 | CAAGAACTCAGGACC[A/T]GCCAAATGGCAACAC | 57626 |
rs150340832 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757618 | ATTTGATTTGGGGAT[A/G]GCTGTCAAATAGGTT | 57626 |
rs150356907 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819109 | TTAAAAGATCCTGAT[A/G]GTGTAGCTTGTCCAG | 57626 |
rs150365803 | snp | A/C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965232 | CAACTCATTATCTAG[A/C/T]AATTCCATCAAAACC | 57626 |
rs150370930 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030019 | TACATAATGGTAAAG[A/G]GATCAATTCAACAAG | 57626 |
rs150379817 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860521 | ATGTTTATAGATTCA[G/T]GAATCCAAAGTCTTA | 57626 |
rs150381015 | in-del | -/TCTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001581 | TCTATGATCTATGTG[-/TCTA]TCTATCTATCTATCT | 57626 |
rs150388870 | in-del | -/AT | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778052 | ATAAAAATGTATAAA[-/AT]AGAGATGGATATATC | 57626 |
rs150418314 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940973 | TTCAATGAGTTAGAT[C/G]ATTTTATTATCATTT | 57626 |
rs150425785 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775924 | TTGAGAGGCCGAGGC[A/G]GGAGGATCACAAGGT | 57626 |
rs150432727 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098171 | ATGTTTTAAACTCTC[A/G]AAGTGTTTTCAGATA | 57626 |
rs150433387 | snp | C/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827725 | ACAGAGCGAGACCCT[C/G]TCTCAAAAAAAAAAA | 57626 |
rs150441953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737351 | TGAGGCAGGAGATCC[C/G]TCCACTCCCGTGGGA | 57626 |
rs150465283 | in-del | -/TTC | 0.132066 | 0.220435 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746350 | ATTTGGCATTTAAAA[-/TTC]TTCTTGCTGAATTGA | 57626 |
rs150467974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039192 | TCCAACCTCAGCTCC[C/G]CAAGCATCTGGGACT | 57626 |
rs150469588 | in-del | -/TCT | 0.32627 | 0.238082 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947079 | GTGTGTGTGTGAAGA[-/TCT]TCTTCCTATTCCGTC | 57626 |
rs150472741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945113 | GCCTCAGCCTCCCAG[A/G]TAGCTGGGATTACAG | 57626 |
rs150477494 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708355 | GGAAACAGTTAAGTA[C/G]TGTGACTAAGTTCAA | 57626 |
rs150478660 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780421 | GTGATTTCTTAAGTA[A/G]AAGAGACATGAAGAG | 57626 |
rs150483102 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69753842 | GCATAGAAATAATTG[A/G]AAAAAAAAATTTTGA | 57626 |
rs150517733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70105118 | TTCAATAGTTTACAC[A/G]TGCCTAATCTCATAA | 57626 |
rs150523194 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844964 | TATTCGATCCAGGAA[A/G]TATTTGCTCCCGCAG | 57626 |
rs150525288 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022397 | TAGTGATACTCACCT[-/A]TTTTGGGGAATGGAG | 57626 |
rs150528030 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942438 | TTGTGATGTTACTAC[C/T]ATTTTCTCTTAGATT | 57626 |
rs150533289 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778539 | GACAGATAAGACATA[A/G]TTCTTGATTGTACAA | 57626 |
rs150536464 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739160 | CTTAACTAAGCTTCA[C/T]AAGTGAAGGAGAAAT | 57626 |
rs150541939 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997891 | CCATATCTTGACTGC[C/T]GAAAATAATAGTGCA | 57626 |
rs150561762 | in-del | -/AATT | 0.0593388 | 0.161704 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789327 | AAGTCTTATTTAATA[-/AATT]AATTAAAAATATAAA | 57626 |
rs150569611 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108935 | CTGCTTCACTCCTGG[A/G]GCCAGAGGCGTACGG | 57626 |
rs150571855 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041054 | ATTTTACTTTAGATA[A/T]TATATTTTTAATTGT | 57626 |
rs150572439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882090 | CATGAGTCAATAAGC[A/G]GCAGAGATAGGATTT | 57626 |
rs150575353 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951173 | AGACATTACTTATTG[G/T]GAAAATTACACCATA | 57626 |
rs150584277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711065 | GTAAAACCAAATTGA[A/G]TTTTTTAAGAAACCA | 57626 |
rs150586636 | snp | C/G | 0.456803 | 0.140473 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783607 | TGAATAAAATGAAGC[C/G]AGAAGGGAAGTTTAG | 57626 |
rs150603710 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70023217 | AAAAAGTTATAAAAA[C/T]ACTATCCTCATGTAC | 57626 |
rs150608399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761572 | TTAATTGAATACCAG[A/G]AAAATACTATGCCAG | 57626 |
rs150610938 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957746 | CTACTTTATAACACA[C/G]TCTCTTTACAAATGG | 57626 |
rs150614308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050686 | AAACTTCTGCTTCTG[C/T]ATTCAAAAAATATTT | 57626 |
rs150616481 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949411 | TTGCTGATTATTAGA[C/T]TGGGGTTATGAATGA | 57626 |
rs150624720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009584 | CTTCTTTGTTATTGG[A/G]TAGTGAGAGTTGGAA | 57626 |
rs150625544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855244 | TGTCAGAGAGTGATG[A/C]CAGAACGGCTGCTGG | 57626 |
rs150627076 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924089 | CCCTGCTGCCTCGAC[C/G]CCCTCTGGACCTTGG | 57626 |
rs150634154 | in-del | -/A | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731035 | AATATAGTAATGCTT[-/A]AAAAAATCATTTTCA | 57626 |
rs150644389 | in-del | -/GTTA | 0.121717 | 0.214577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851210 | TTTTTATAAAATTCT[-/GTTA]TTTATAATTACATTT | 57626 |
rs150661896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896441 | GGACACCTTGGCAGA[C/T]GGGAGAATCTTTAGA | 57626 |
rs150663770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962439 | CTGTTCATTCTGTAT[A/T]ACTCCTCTTCTTTCT | 57626 |
rs150665520 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055620 | ACTTCTTAAGACATA[A/G]GTAGAATAATAAGAC | 57626 |
rs150676363 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786721 | TAAGTCAAATTGTCC[C/T]TGTTTGCAGATGACA | 57626 |
rs150678235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858472 | ATAAAAATTAAATTA[C/T]TTTTCTCCTTGTAAA | 57626 |
rs150686477 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995395 | AGTTATTACTTGGTC[A/T]ATTTAATTAGAAAAT | 57626 |
rs150692325 | snp | A/G | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840248 | TTTTTTTTTGAGACA[A/G]ACTCTCACTCTGTCA | 57626 |
rs150694879 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095694 | TAGAAACATTCCAAT[A/T]CCACTCTTTTAGTTA | 57626 |
rs150697682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069420 | TTTTAACTGATAAAT[C/T]ATGTATGTCTTTTAA | 57626 |
rs150712429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866427 | ACTCTAAATGAAAAC[A/C]CATTACTTATTAAGC | 57626 |
rs150733045 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877736 | TTATATTTCAATAGA[A/G]GACAGAGAGCAACAG | 57626 |
rs150738868 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715871 | CAAAATTGTTTTGAT[A/G]CTCATTTGTTAATAG | 57626 |
rs150738977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969823 | CACATATTTAGTTCT[A/G]TTAATGCTAGAGAAC | 57626 |
rs150747181 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774487 | TTTTGCCATATCCTC[C/T]CTCTCTTCTCAGGTG | 57626 |
rs150779418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078649 | CCTCTTTGCCTTCAA[A/G]TCTATAAAAGAAGAA | 57626 |
rs150794895 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749578 | AAGAAACAAACTATC[A/G]TTAATTTTCATGTAA | 57626 |
rs150819518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928337 | TAAACATCCGATTCC[C/G]TAACTTTTCAGGGAG | 57626 |
rs150823464 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087067 | AATTACCAGTGTTTG[C/T]GTACAGTCCAGTGAG | 57626 |
rs150833565 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045019 | ACACCTAACTCTCAC[A/G]GGTGCTATGTATAAT | 57626 |
rs150834392 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815542 | GAAACAAGTAACACT[A/G]GGGATTCCAAAACTG | 57626 |
rs150835420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887385 | TTTGGTGTTCTCTAT[C/T]GAGCAGCTTTTTCAT | 57626 |
rs150835487 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980082 | GGCTGAGAACTGACC[A/G]ACATGCTTTACTGTT | 57626 |
rs150854632 | in-del | -/TTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038582 | GGGATTGTCATTAAT[-/TTT]TTTTTTTTTTTTTTT | 57626 |
rs150864774 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019944 | GACTTTCAGGAGTGA[A/G]TTAACTCTCTTCTGC | 57626 |
rs150871139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729309 | TTTGGTCTTGAATCC[A/G]TCAGAACACACTCAT | 57626 |
rs150873130 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934095 | GTTTTTAAAATGGAT[A/G]TAACACTTGCCTTGC | 57626 |
rs150875874 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091799 | AAGCTCTGTAGGTGC[A/C/T]GCCTAAACTACCTTA | 57626 |
rs150887492 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820655 | CTCTGGAGATTCAAC[C/T]TCATCCTTTACTCCC | 57626 |
rs150892748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872883 | ATCCTCCCCAATGAC[A/G]CAAACATCTTTCATT | 57626 |
rs150907396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770047 | CTGGACTGTGAACAG[A/T]GGGAATGAGATAGAA | 57626 |
rs150909777 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833842 | GTATACATATATATA[C/T]ACACACACATATATA | 57626 |
rs150910773 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862246 | AATACAGTTCCCATT[C/T]ATAATAAATGTATGT | 57626 |
rs150918779 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991994 | AACATCAGCTGTGAA[C/G]TTGCTAGGAATGCAA | 57626 |
rs150927945 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089517 | CAGATTGTTAAAATA[G/T]CTTGCGTGATACAAC | 57626 |
rs150939411 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724694 | ATAGTTCAACAAAAA[A/T]TCTTGATTAAAGCCA | 57626 |
rs150939865 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790055 | GCTTCTCTTGGTGTT[A/T]GCCACTTCTGACACA | 57626 |
rs150940188 | in-del | -/AG | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999559 | ATCGATAGGTAAGTA[-/AG]AGATTGGGATGATTA | 57626 |
rs150958412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100570 | GAACTCTTGACCTCA[C/T]GATCCACCAACCTTG | 57626 |
rs150963550 | in-del | -/ATATGGGTGAGGCC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69862698 | ATACTAAATGAGGTA[-/ATATGGGTGAGGCC]TTAATGCAATAAGAC | 57626 |
rs150964051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829552 | AACACCATCAGAAGA[C/T]CACACTAGCTCACCA | 57626 |
rs150978021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837061 | ATATAAAAAGGTTTT[C/T]TAAGACAAAATTTTT | 57626 |
rs150982100 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936370 | AAGGCAGGTGGATGA[C/T]CTAAGGTCAGGAGTT | 57626 |
rs150991125 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731874 | GGAAAATCACAAGTA[A/G]TAAATAGAAAAACAA | 57626 |
rs151000682 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874895 | TTTATCCTAAGAGCA[C/T]AAATCTTGTCAAGTA | 57626 |
rs151013296 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032875 | TGCAAACGTAATTGC[A/T]GTTTTGCCATTTTTT | 57626 |
rs151013525 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771422 | TATCTCCTCATTTTA[A/C]ATTTTTTAGAGGGAT | 57626 |
rs151052394 | snp | A/G/T | 0.00915269 | 0.0671332 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847973 | ATTTGCATTAAAGCA[A/G/T]TCTAAGACATTCCAC | 57626 |
rs151062483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755855 | GGGTAGTGGAAAAAT[A/C]ATACGTTTTGAAAGC | 57626 |
rs151066739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999513 | AAGTATAAACTTTCC[C/G]TTCTGCATTTTGGGC | 57626 |
rs151067708 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741126 | AGCTTAGAAAATATG[A/C]CATCTTTCATATTAT | 57626 |
rs151070719 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69944539 | GTCTTGGGGATCACC[C/T]AACATAGCATTCTAA | 57626 |
rs151077656 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987881 | AATTACTATGAAAAG[A/G]TACATTAAATGTAGA | 57626 |
rs151092065 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952173 | ATGTCCTATTACATC[A/G]TTTTTGAATTAGTCA | 57626 |
rs151097000 | snp | A/G | 0.116838 | 0.211584 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042965 | GGCTGGAGTGCAGTG[A/G]CATAATCCCAGCTCA | 57626 |
rs151098591 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865424 | ATAACTAAGAATAAC[-/A]TATATGATTCTAAGG | 57626 |
rs151103672 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782382 | GCCTCACTCGGGAAG[C/T]GCAAGGGGTCAGGGA | 57626 |
rs151104819 | in-del | -/AAAT | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908587 | GATTCATTTATAGAC[-/AAAT]AAAAGGAAATATATA | 57626 |
rs151109445 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047063 | TAATACAACCAAACC[A/C]ACCAAACCTTGCAAC | 57626 |
rs151140931 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703228 | TCGTCTGGTAATGTC[-/A]ATAGCCCTCTTAACA | 57626 |
rs151141506 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958395 | GAGTGTTTCCCATAT[C/T]TTAATATGTACAATT | 57626 |
rs151142564 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024863 | TTAGTACCAGAAGAG[A/T]CTTCCTGTGCCTCTA | 57626 |
rs151145059 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926782 | GAAATCCCGTCTCTA[C/T]TAAAAATACAAAAAA | 57626 |
rs151150393 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763918 | CTTACAAAAAAGTAA[A/C]CTGAAGTAACCATTT | 57626 |
rs151155955 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69856121 | TCAGGAATGTTTGAA[C/T]ACTGTGCAACTTTGG | 57626 |
rs151172270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064737 | TTAGCCACCTGCTAA[C/T]GCTAATGTGCCACAG | 57626 |
rs151173500 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794095 | CATGAATATTACCTT[C/G]TCATTTAAGCTACCA | 57626 |
rs151181958 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066303 | CAATGAGAGATTTAC[-/T]TTTTTTAAAAATCAG | 57626 |
rs151192527 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897845 | ATAAGAATAGCAGAT[A/G]ATGAGATCATTAACC | 57626 |
rs151194755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965080 | GCTTTTTGATGGCTT[C/T]AAAAATAAAATACAA | 57626 |
rs151196414 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859970 | TCTGAAGGCCTAAAC[A/C]ACAACTATTTAGTAT | 57626 |
rs151210534 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842294 | TTAGCAAATTATTTA[C/T]GCAAGAGAGGACAAA | 57626 |
rs151213768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910342 | GTAGAATGGTTTGCC[A/T]CTAGGTTAAGGCCCA | 57626 |
rs151214473 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106912 | GAAGAACACCATAAT[C/G]TCAGGAATATGAGAA | 57626 |
rs151224191 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071585 | CAGGCCATAAAACTG[A/G]CCTTAACGAATCAAA | 57626 |
rs151225953 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996164 | AAAAATTAGCTGCGC[A/G]TGGTAGCATGTCCCT | 57626 |
rs151226618 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736607 | CTGTTTATAGCAGCA[A/C]AATTTGCAATTGCAA | 57626 |
rs151228173 | in-del | -/TGTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730268 | GTACTAACACTTTAA[-/TGTG]TGTGTGTGTGTGTGT | 57626 |
rs151228429 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69799641 | TAGTGACAAATAACA[C/T]AGATTTGTTATCTTA | 57626 |
rs151233862 | in-del | -/A | 0.14933 | 0.228835 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835823 | ATAATGGACAGAATG[-/A]AAAAAAAATAAGTGA | 57626 |
rs151263939 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809715 | AACATTGAATATAAA[C/T]AGTCTAAACACTCGA | 57626 |
rs151266221 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70079736 | GTGAACTAGGTAATA[C/T]TACTCTTTCTCTTTC | 57626 |
rs151272150 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718186 | AAAAGGAAAATTTTT[C/G]TGCTGTCAGTGCTAT | 57626 |
rs151280182 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775719 | TTTTTGATACAGTGT[C/T]GTGCTCTGTCACTAG | 57626 |
rs151301481 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922290 | AAAATTTTAAGGGTA[C/T]AGAGGAGGAAAAGAT | 57626 |
rs151310011 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69984086 | AAATGGTTCATGACA[A/T]TGGTCTGGGCAAGGA | 57626 |
rs151310340 | in-del | -/ACAAAGGC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69983910 | ACGGCTGATTTTTGA[-/ACAAAGGC]CAAAGATCCCACAGT | 57626 |
rs151314787 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753204 | GTCTTAGGGACTCTT[C/T]TACTCAGTGAACCCA | 57626 |
rs151315058 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813423 | ACACATGTATACATA[C/T]GTAACACACCTGCAT | 57626 |
rs151317522 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084301 | CTATACCCAGCATAG[A/G]GGATGTACATGAACA | 57626 |
rs151330547 | snp | A/G | 0.000619719 | 0.0175919 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69701744 | GGCACCTGCTCTCCC[A/G]ATATTCAAGGAAGCC | 57626 |
rs180678944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724875 | GCTATATATTAAACC[A/G]AATTTGCCCAGTAAA | 57626 |
rs180687384 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746914 | TGATGCATTTGTGTA[A/T]GCCTCCATAAAAAGG | 57626 |
rs180691975 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717668 | TAAGATATTCAAGGT[A/T]AAAGTAGGAGGCTCA | 57626 |
rs180693366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767716 | CCTTTCGTTTTCTCA[A/G]TATTTTGTCTTAATT | 57626 |
rs180693602 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101490 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTTACT | 57626 |
rs180700114 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108560 | GGAGGGAAGGCTTCA[A/G]TCTTCTTTATGCAAG | 57626 |
rs180705510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083343 | ATGTTCTTATTTCTT[C/T]CCTTCTTTTTTAGAG | 57626 |
rs180709012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091610 | ATCATTCCCTGGCCT[C/T]CTTCTACCTTTCCTT | 57626 |
rs180720314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801920 | AAGAACATGCAGGTT[C/T]ATTACATAGGTATAC | 57626 |
rs180724734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785927 | ATGGATAAATTCCTC[A/G]ACACATACACCCTCC | 57626 |
rs180725391 | snp | A/C/G/T | 6.95636e-05 | 0.00589729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707820 | CAATGACAATAGTAC[A/C/G/T]TAACATATTCTAATC | 57626 |
rs180728606 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779507 | CCCTTCTTTCCTGTC[C/G]TTTTTCCTTTTCTTT | 57626 |
rs180730872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856619 | ACATTTTGCTCATCT[G/T]TCTGTTAAAAACTTT | 57626 |
rs180735433 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736838 | ATAGTATATTCTCTC[A/G]TAAGTGGGAGATAAG | 57626 |
rs180742900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757133 | CTAAATCTTTTAGAA[A/G]CCTACATTCAAGAAT | 57626 |
rs180743109 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838168 | ATTGAAATAAGTTTT[A/T]TTTTTGTTCTGATTT | 57626 |
rs180745514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823253 | CTCAAAATGTCTCAG[A/G]GAAATAGGAAATGTT | 57626 |
rs180761387 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812640 | AAAAAACAAACAACC[C/G]CATCAAAAAGTGGGC | 57626 |
rs180767052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876145 | AGACACTTATCAAGG[A/G]GTAGTTTGGGGAGGT | 57626 |
rs180777027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795344 | TACAGTGCTGGGAAC[A/G]TGAACATTGAACAAG | 57626 |
rs180781028 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915435 | GCCCTCAGAAATAAT[G/T]CTGCATATCTACAAC | 57626 |
rs180792447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869042 | GCCTGATAAGGAAGC[C/T]AACGGCAGCTAGAAA | 57626 |
rs180794326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847595 | AAAGTACTAACTCTT[C/T]TAAAACTATATCCTT | 57626 |
rs180806792 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885741 | ATAGGTTTATCAAAA[A/C]CCTGATATATGGCCC | 57626 |
rs180811830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923090 | CCTCCTTACCCTCCC[C/T]AGAATGAGACACTTA | 57626 |
rs180814618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831534 | TTCAAGGAAGAATTG[A/G]TACCAATTCTATTGA | 57626 |
rs180820945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894185 | TCTTATGGCCACCAG[A/G]CCAACTTCTATTCAC | 57626 |
rs180830801 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906431 | ATTAAGGTATCGGCT[A/G]TATTTGCAAACCGGG | 57626 |
rs180834232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960306 | TGTAAAAAATAAAAC[C/T]CCTTAAACTACGTTC | 57626 |
rs180844019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943814 | AGGAATTTTACCTAA[A/G]TTGTTCAGTAAAGTT | 57626 |
rs180847380 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976195 | CTTAATTATACTATT[A/C]TAAATAGAATTCTTG | 57626 |
rs180862158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051357 | TGGTTACATCTATTA[C/T]TGATAATTGCCTTCA | 57626 |
rs180863727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011806 | ATTTTGAATTAAATT[C/T]GGGGGTTCCGTATTT | 57626 |
rs180866268 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023067 | TTTCAGTCACACAGA[A/C]CTTTATTCACTATAC | 57626 |
rs180867419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992869 | AAGGCATATAGTCAA[C/T]ATGAGATAATGTTTT | 57626 |
rs180869015 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060873 | AAAATGTGGTATATA[G/T]AAACAATAGAGTACC | 57626 |
rs180874896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077004 | GTGTGGAGAAACTGG[A/C]ACTGTCATTCATCGC | 57626 |
rs180897700 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031759 | TTCCTCCAGTTGTTC[C/T]AGAGTGATAGTATGC | 57626 |
rs180899504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003155 | ACTGAAATAACAATT[A/T]TGAGCATACAAACTA | 57626 |
rs180905913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703551 | AGAGAGTTTTTTAAG[A/T]CTGCAGTAGCATATA | 57626 |
rs180910147 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068626 | AAATGTGCCTATTTT[A/G]TGAGTGGAAATAGAG | 57626 |
rs180920622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041709 | CTACCCCAGTGGAGT[G/T]GGGTAGAAACGCCTT | 57626 |
rs180941676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763072 | TTTTTCCATGATTTG[C/G]AATAAATGAGGCAAG | 57626 |
rs180950085 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104884 | TTACTTTGGAAATGC[C/T]GTCTTTTCTGGGCAG | 57626 |
rs180958114 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70087738 | GGCCTTCTGATGGAG[C/T]AATAAAATAGATGCT | 57626 |
rs180961500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721485 | TCTCAGATATTTTGG[A/G]TTCGCAGATGAAATT | 57626 |
rs180966478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741985 | TAGCAAACACAGATC[A/G]CTTATGATCCACCTA | 57626 |
rs181005115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752174 | CAATATGTTGAAGAT[C/T]ATCATAGCAATGTAT | 57626 |
rs181010644 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775356 | GTCTTGTAAAAACAA[A/G]CATCTATTAATATAA | 57626 |
rs181011121 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096072 | TGCATATATGTACCA[C/T]ATTTTTTATCCATTT | 57626 |
rs181017312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798587 | TGTTTATTAACATGT[A/G]TAATATTTTAAACAG | 57626 |
rs181023658 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731729 | TTTTCTTTCTTATCT[A/T]ATAGCTTTTTAAAAA | 57626 |
rs181027732 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69817875 | GTCTGCATTCATACA[A/G]TCTTCATTCCTAGAA | 57626 |
rs181030510 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827270 | TTTCTTATATTTCAA[A/C]TATGTTTTCTAAAAT | 57626 |
rs181030705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808992 | ACTAATCCTTTAAAT[C/T]TACCTAGTCAGAAAA | 57626 |
rs181034530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871937 | CTCCAAACTTTTCCA[A/G]TCTTTGCCCGTTACC | 57626 |
rs181037223 | snp | A/C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783065 | TGATACCCAGGCAAA[A/C/T]GGTCTGGAGTGGACC | 57626 |
rs181042929 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834182 | AATCTCAGAAATCAC[A/C]ACTAAAGAACTTATC | 57626 |
rs181050370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790816 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 57626 |
rs181060092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852157 | AGACTGACTAGCTAA[C/T]GAGAAAAAGGTACTA | 57626 |
rs181072301 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928024 | AGGCTACAGTTTGGG[A/C/T]CATGTCCTTGTGGTT | 57626 |
rs181072516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842822 | TGAATAAAGAAAATG[C/T]GGTATATATACACAA | 57626 |
rs181074110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863837 | ACTGTCAGTAATAAT[G/T]CTTTCTCACTAATAT | 57626 |
rs181078828 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910602 | CCTATCAAACATAGA[C/T]TGAGAAATTATGGGA | 57626 |
rs181081363 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889571 | CCTATGTAACATATA[C/T]GCACCCTTACTCTTA | 57626 |
rs181084459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947418 | ATCCAGAGGCAGTAT[A/G]TCAATGTAATAACTT | 57626 |
rs181089088 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899392 | CCTGGTTCACTCATC[C/T]AAAATTGTGTGGCAA | 57626 |
rs181091208 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064074 | GCTTTAGTTAGAGGA[C/T]GGATTAATGGACACA | 57626 |
rs181098524 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69964870 | TTGGTCAATTTCCAT[C/T]GACTGATTTTTGTTT | 57626 |
rs181105923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920465 | CCATGAAGAATTTGG[C/G]AAAGTTACTTAACAC | 57626 |
rs181111262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939734 | TGGAGCCTATGCGCC[C/T]CTCTCCTCATACCTC | 57626 |
rs181117161 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69954971 | TGTTTAAACACCCTC[G/T]GAAAATTGCTTAAAT | 57626 |
rs181125977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989032 | ACGATGAAATCTTTG[A/G]GAGTTTCTATGTTCA | 57626 |
rs181134303 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973353 | TGATGATATAATTAA[C/T]ATAAATTAAACATAT | 57626 |
rs181140219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006368 | TTGAATTTGGTTTGC[A/T]AGTAATTAGTTGAGG | 57626 |
rs181153040 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028303 | AGGGAGATTACTTTG[C/T]GGCCCATGGACAGCC | 57626 |
rs181164233 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044950 | CAGAATAACCTTGGG[A/T]AAGTCATTTAACCTT | 57626 |
rs181195687 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072590 | AACAATAATTATACA[C/T]CTGTGGCCAGGTAGA | 57626 |
rs181226484 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109431 | CCCAACAGAGCATAG[G/T]AATCAACCACTGAAG | 57626 |
rs181240220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756122 | ACATAAGTAAGTTGA[A/C]CCCCACCCTTCCCAG | 57626 |
rs181245967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092117 | TTCCACCAGATGAGA[A/C]ATAAACCAGCTGGCA | 57626 |
rs181262396 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735949 | TGTGAATATGTATTC[A/T]TTGTATATGTGTATC | 57626 |
rs181270393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716997 | TCTGTTCCATAAACT[A/C]TTCTAAAGTCCTCAT | 57626 |
rs181270928 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952068 | AAGTTAAATAAATGT[A/G]AGCAAGGGGGTTTGA | 57626 |
rs181281683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969404 | CCTCAAATATTTATT[A/G]CATACCAATTAGATA | 57626 |
rs181284779 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787166 | AAAAACTACTTTAAA[G/T]TTCATATGGAACCAA | 57626 |
rs181295824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984871 | CCCAGCACTTTGGGA[A/G]GCCAAGGTGGGCGGA | 57626 |
rs181297914 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794913 | ATGATAGATTAAGGA[A/G]TATCAACATCTATGC | 57626 |
rs181300140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868218 | ATATTTAGTGAAAAA[A/G]TATGCAGAAAGCAGC | 57626 |
rs181302914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885520 | GATACTTTGTTTATG[A/G]TACCTACAATGTAGG | 57626 |
rs181306502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021982 | GCAGAGCAGAAACTT[C/T]ATTTTAATGAAGTCT | 57626 |
rs181307759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846121 | AAATCCTGTTCTATG[A/C]TATCCAAACGAATTA | 57626 |
rs181312333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802847 | CTTCCTTCTTTAACT[C/T]GGTGTCTGAGGGGTT | 57626 |
rs181312568 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041346 | TTTTCTATTACAATA[G/T]TATGGATTTAATTTA | 57626 |
rs181314758 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824029 | GTATATAATAGTCTA[C/T]GAGAGTATGTTTGTA | 57626 |
rs181315688 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060622 | GCTGAGGCGCGTGGA[C/T]CACTTGAGGTTAGGA | 57626 |
rs181322297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076564 | CCTCGGGTTTGACAA[C/T]GTGACAATGAGTTTT | 57626 |
rs181327949 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895172 | AGGTAGTCTTTAATT[A/C]TAACTTCAATAATTT | 57626 |
rs181332244 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905899 | GATGAAATAAGTCAA[A/C]GTTTCGAAAATGTAC | 57626 |
rs181332888 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778876 | CAATCTTGGCTTATC[A/T]CAACTTCCACCTTCC | 57626 |
rs181335573 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858251 | TCTTCCTTCAACTGA[C/T]ACCCTCTTGGGGAGG | 57626 |
rs181336667 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922395 | AAATATCTGGTATAG[C/T]AAAATAGCAGGTATT | 57626 |
rs181345026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959615 | TGAGATGTTAAGTCT[G/T]TTTAAAAACCTCTTG | 57626 |
rs181355089 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991711 | CCAGATGGATTCACA[A/C/G]TCAAATTCTACCAGA | 57626 |
rs181403204 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838864 | CTTAATCTTAAATTA[C/T]AATAATTAAAGCTGA | 57626 |
rs181442399 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713688 | TAGGGTAGATCCTAA[C/T]ATATTTGAAATGAGA | 57626 |
rs181452366 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730283 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 57626 |
rs181453080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943023 | GAAGAATCCATACTA[A/G]TTGTTCTGCAGAATT | 57626 |
rs181459806 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877667 | CACTATCATTTTCCC[C/T]TTTTCTCTGGTCTAT | 57626 |
rs181460379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853844 | ATGAAGACATTACAT[C/T]TTCTTCAAAGTATGT | 57626 |
rs181467227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834709 | CTAAAATTAGAAAGT[C/T]TCTGTTGCCAAGTTG | 57626 |
rs181477717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890955 | ATACAACGAAGAAAA[G/T]TATTCAAAGAGCTGT | 57626 |
rs181484180 | snp | A/C/G | 0.0174175 | 0.0916809 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915914 | AAAAAACAAACAACC[A/C/G]CATCAAAAAGTGGGC | 57626 |
rs181484677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912757 | GGATTTTCTGTCGTC[C/T]AGCCTTTTCTTTTTT | 57626 |
rs181485950 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975885 | AGAATAACATACAGG[A/T]TTTTATCATTTTCTT | 57626 |
rs181486445 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873145 | GGACACTGAGGTCCA[A/G]TGAAACTTAATATAC | 57626 |
rs181487453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790224 | TTCAAATATCTACTA[A/C]TAATAAGAACACTGG | 57626 |
rs181494575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774232 | TATACAAACTCACAG[A/T]TACAAATAGAGTTCA | 57626 |
rs181498853 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69702293 | TGCTTATTAAAAATT[G/T]TCCATCTTATGACAA | 57626 |
rs181498868 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70096823 | TGGCTACCTCCTATT[A/G]CAGGGAAAGCATAGA | 57626 |
rs181499135 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973045 | TAGGATTTCCTTCAA[A/G]GCCTAAAGCACAAAT | 57626 |
rs181505598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751528 | GGCAGAAGAAACACT[C/T]GTGTTGTGATAAGAA | 57626 |
rs181536515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965513 | GTTCCCTGAGACACA[A/G]TATTAAAACTAGGCC | 57626 |
rs181538631 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988772 | CTTCCTTTGACAAGT[A/G]TCTTCATGTCTTTGC | 57626 |
rs181539703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948405 | ATGCCTAACTCTATC[A/G]TTATGAAAGGGGTGA | 57626 |
rs181544914 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70005886 | ATCATGAGATCTACT[C/T]TCTTTAGCAAATTCT | 57626 |
rs181550097 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044538 | TTTTTGTATCAGTTT[A/G]TGGAAAATTTCTTTT | 57626 |
rs181555951 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063892 | TAGGTGTGTTTATAT[G/T]ATTGGATGCTTTCTT | 57626 |
rs181561848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081282 | TTAACAACTTAAAAC[C/T]GTACACATATTTATT | 57626 |
rs181563492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842123 | AGAAAGTTCTCATAA[A/T]GAGTGGTCTAAGCAA | 57626 |
rs181617216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101048 | ATGAGAAGCATAATA[A/C]CTGAGGATACATAAA | 57626 |
rs181624840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881371 | TGTTTTATATTTTTA[A/G]TAACATATGGATTAG | 57626 |
rs181629244 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082644 | TTAAATACAGGTACA[G/T]GTGCAGGTTTGTTAC | 57626 |
rs181639814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720809 | GGGGCAGAGGCTGAG[A/G]TGAGAGTGGTGGTTC | 57626 |
rs181652101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716490 | TTTTTCTTTCTGGTC[A/G]AATTTGCAATATGAA | 57626 |
rs181656941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735286 | ATCAGAGACTATAAA[G/T]CACTATAAAGGTTTT | 57626 |
rs181666974 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857689 | TCTCTGAAGTATTTC[A/T]GGGTTAAATTTAAGG | 57626 |
rs181677570 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954600 | GTGGTAGATACATAA[A/C]CCTTACTCCTAAATA | 57626 |
rs181680946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794660 | GAAATAGGAACAGTA[C/T]GTAGCCTAACAGAGA | 57626 |
rs181681931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919839 | AAAAGGTCACATATA[C/T]TTATTTCAGTTCTGA | 57626 |
rs181687090 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778628 | TAAAATTTTGCCTCT[A/G]GAAATGAGTAACAGG | 57626 |
rs181689503 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894797 | AGCTCCACAAATTCC[C/T]TAATTTCTGGGATTT | 57626 |
rs181694814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826837 | TTTAAATTTTATAAA[C/T]GAGTGTTTAGGATAC | 57626 |
rs181702909 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755345 | TTCACTAAAAGGTTT[C/G]TGGATGCCAGCATCA | 57626 |
rs181709569 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915591 | TTATACAAAAATTAA[G/T]TCAAGATGGATTAAA | 57626 |
rs181716689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877231 | ATTCATTAGAAAATA[A/G]TATAGCAAAAATCTG | 57626 |
rs181718878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018123 | GATATTGAAATCTAC[A/G]AGTGAATAACTTACG | 57626 |
rs181724333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934207 | GTGCCATCACCAGCA[C/T]CATTGGTGGTAAGGC | 57626 |
rs181737491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055456 | AAGGATGTTAACAAG[A/C]AATAAGAAATCCTCA | 57626 |
rs181737848 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898342 | GCCTGAGTTCCTGTG[C/T]ACCCCAGAGGAGATC | 57626 |
rs181738991 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863125 | AAGACCTTCTATAAC[A/G]TTCATGGTAATTCTC | 57626 |
rs181746204 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968363 | CAAATATAAACAAAT[A/G]TATATATAAATATAC | 57626 |
rs181797639 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109649 | AACAGCTGGACTGCA[A/C]TCCCTTGTGCCTTGA | 57626 |
rs181810701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993513 | AATGAAAAAGAGGTC[A/G]GTGTATTATTTTTCC | 57626 |
rs181820568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012433 | AAATTTAACTTATTT[G/T]TTCCCAAGGTAGCTT | 57626 |
rs181829200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032455 | TTGAAGAAATGAGTA[C/T]AGTGGATCCCAATAT | 57626 |
rs181834172 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051567 | ATTTATGAATGAAAT[G/T]TAATTCAATAGAAGG | 57626 |
rs181836640 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069083 | AGATTTTATCAAAAT[A/C]TAATTGACCTGAAGG | 57626 |
rs181848016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743034 | GATCCTGAAATCAAC[C/T]TTTTACTGAGCACCA | 57626 |
rs181855775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802453 | ATCCCTCATATTGTC[A/T]TATGCCCAATTTCTG | 57626 |
rs181857664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763818 | AAATGTTAAAGAAGA[C/T]AGATCCCAAAACAGA | 57626 |
rs181858472 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725871 | AAAGAGCTAGTGCCA[C/T]AGCACTAGATCTTTT | 57626 |
rs181866061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768666 | TTAAATCTCTTATAC[A/G]TTGATGTTGAGCAGA | 57626 |
rs181877343 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838553 | ACCATTCTTATACTT[A/C]TTTATAATTGTCTAT | 57626 |
rs181878394 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69819315 | TACTAATTTAAATTA[C/T]ATGAAAATTAGAGGC | 57626 |
rs181879416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997162 | GTAGACAGAGGTTGC[A/G]GTGAGCCAATATCAC | 57626 |
rs181888072 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799044 | CAGTGAGCTGAGATC[C/G]TGCCACTGCACTCCA | 57626 |
rs181894322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783351 | ATGAGTTGAGAGAAG[A/T]AGTCTCCAGACGATC | 57626 |
rs181897386 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69852733 | AAGGTAGATGCATCA[G/T]GCAAGTCAATAAGGG | 57626 |
rs181904357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834468 | CACTTGGCTTTTCAC[A/G]TCTTCAAAATATTAC | 57626 |
rs181908037 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713187 | TAATTCAATCTAACA[C/G/T]TTTCTAGTTTGATTC | 57626 |
rs181919234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908219 | AAGAGAAGAGACGCC[A/G]GAACCATGGGGGTTA | 57626 |
rs181932654 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70037503 | CAATATGACTTTCTT[C/T]TCACTTATTTTATTT | 57626 |
rs181939130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944090 | GGTATTTGAGAACTT[A/C]GATTTCAAGAGGATT | 57626 |
rs181948133 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70002099 | ATAGAACAAAATTCA[G/T]CACTCTTTATAAGAT | 57626 |
rs181950058 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976613 | ATGACAATTGCTTAA[A/G]TAACCTAAAATTAAA | 57626 |
rs181963660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040861 | TATGGAACCCCAAAG[A/G]CACAAATATTTGATA | 57626 |
rs181966624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071971 | AAATTCACAACAGAA[A/T]TCAATTTAATTGAAA | 57626 |
rs181980072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074590 | AGTTTAAGAAATGTA[A/G]GGTTAAACAATGATA | 57626 |
rs182001577 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955310 | TTCAAATGTTTGGCA[A/G]TAAGCAGAAGCTATC | 57626 |
rs182017311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973823 | ACTAAAGTTTTAAAC[A/T]ATAGTGTTAAAAATT | 57626 |
rs182018913 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70017219 | CACACCTCCTACTTG[C/T]CATGTTGCCAGTGAT | 57626 |
rs182020227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036386 | TTTCAGAACTTTTAA[A/G]TTACCTTTTGTAGTT | 57626 |
rs182026438 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989557 | GCTTTGGGCAGTATG[A/G]CCTTTTTAATAATAT | 57626 |
rs182028975 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007056 | GAGAAAACAACCGGA[C/T]TGAAATTATGAATCC | 57626 |
rs182029246 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055150 | CTCCCAAAGGTCAAG[A/G]ATAAAGAAAGGGTCA | 57626 |
rs182036854 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70071768 | GGTAAACCTAAAAAT[A/T]TTTTGGGCTAAATGG | 57626 |
rs182045534 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092835 | AATTAAACAAATAGA[A/G]GAGTAGCCACGCTTT | 57626 |
rs182051362 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722557 | ATGAATAAATTCTCA[A/G]CAGCACTAACCATCA | 57626 |
rs182065677 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092592 | CACTTGATATTATAA[C/T]GATTCGTAGAATGTA | 57626 |
rs182082662 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087422 | GTAGTAAAAACGGCA[A/T]AGTCATGTGTTACAA | 57626 |
rs182086815 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789829 | GCAAAGAAGGAAAGA[A/T]AGATTTTGTTTTGTA | 57626 |
rs182106934 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708158 | TGAAGCAGAAGAAAT[A/G]GTTAAAAATCTGGGA | 57626 |
rs182117852 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786013 | AATTGTGGCAATAAT[A/C]AACAGCTTACCCCCC | 57626 |
rs182121407 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751009 | TGACAATAACTGCCA[C/T]AGTGAAACATGACAA | 57626 |
rs182129017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747956 | GCAAATATTTAATAT[A/G]ATAAGCCAAGGAACA | 57626 |
rs182140978 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826540 | AGCCAAGATCCTGCC[A/G]TTGCACTCCAGCCTA | 57626 |
rs182154088 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788500 | GGAACATCACACTTC[A/G]GGGACTGTTGTGGGG | 57626 |
rs182165887 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823818 | AATCATTGAAATTTT[C/T]TCTCTCTCTCTCTCT | 57626 |
rs182182979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839801 | AGTATATTGTGTCTA[C/T]TTTTTGCTATAATAG | 57626 |
rs182186644 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69925862 | ATACTGTGTGAGTTA[A/T]GGTTTTTACTTTGCA | 57626 |
rs182186824 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824659 | AAAAGACTACAAAAT[G/T]TGTGATTTCCATTTA | 57626 |
rs182190357 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69782268 | CTTTCTGCATTTCCA[A/T]CTGAGGTACCGGGTT | 57626 |
rs182191933 | snp | A/C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890645 | TCTTCCACACACACA[A/C/T]GCACACACACACACA | 57626 |
rs182192643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803557 | TCAGTCCATGAACGG[C/T]TACGCTATATAGCAT | 57626 |
rs182197621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760268 | GCCTCAGCTGAGGAC[C/T]TACCTTTTGTAAACA | 57626 |
rs182199969 | snp | A/G/T | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945025 | GAGTCTCACTTTGTC[A/G/T]CCCAGGCTGGAGTGC | 57626 |
rs182202022 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877874 | TTACCATAACTTAAT[A/G]TGCTAATTTATAATT | 57626 |
rs182208259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69977797 | AGTAAAGTGTAAACA[A/G]CAACAAAAAACATTA | 57626 |
rs182209112 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928971 | AGAAAAATATTTATT[A/C]ATTCTTCACCAATTA | 57626 |
rs182209512 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923523 | ATGCTTTTATTTATA[C/T]TTATTATTTTTAAAG | 57626 |
rs182211623 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963164 | ACCCCAGGGCTCAAA[A/G]TGATCTGCCTTCCTC | 57626 |
rs182218001 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965162 | TTTTATTGCATTTCA[C/T]TTTACTGTGCTTTGC | 57626 |
rs182220448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984062 | AATTATTAGAGGTAA[A/T]CATAGGGAAAATGGT | 57626 |
rs182222412 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996042 | TGACGTGGTAGCTCA[C/T]GCCTGTAATCCCAGC | 57626 |
rs182222943 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994179 | ATATGGAAGAATCAG[A/G/T]CCCCAAATCTAACAG | 57626 |
rs182225930 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013740 | GATGTATTATTTTAG[C/T]TCTAGTGGAGTAGAA | 57626 |
rs182229004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034090 | AGTTCTAAGAATCAC[C/T]TCAAGTGCAGCACTG | 57626 |
rs182232309 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960989 | AATTAGAATCTCTTT[A/T]CTTTCCTAAGCAAAC | 57626 |
rs182238302 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052455 | AACTACAAGAAAATT[A/T]AAAAAAACCCTTATA | 57626 |
rs182242824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021693 | TCTGGATTTGGGGCA[A/T]CCTAATAGGTGCCTC | 57626 |
rs182243602 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106111 | CATATAGGTTATACA[A/T]ATATAATTTTATCTA | 57626 |
rs182248582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860222 | TGGAGTGGTAGAATA[C/T]ATACTTTCTATACAC | 57626 |
rs182250534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089930 | ATGTATTACATTAAA[A/G]TAACCAAAGCTAGTT | 57626 |
rs182260835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059722 | ACTCACAGTTCCACA[A/G]GCTATACAGGAAGCA | 57626 |
rs182265267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895702 | GGAATAATCTGTTTC[C/T]TTCTTTTTTCCTTTT | 57626 |
rs182270814 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028788 | CTGAGACCAACCTTC[A/G]CAATGTGGCGAAACT | 57626 |
rs182300963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066142 | GCAAATTTGCCCTGT[A/G]GTTTACCAGCTGTGC | 57626 |
rs182345660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067865 | ACCAGTGGAGCAAAA[C/T]TTTACCCAAACATAG | 57626 |
rs182365670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104062 | CATCACTATAAAATG[C/T]AAGAATATAAATATT | 57626 |
rs182367769 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69845290 | ACAAAACATATTTTG[G/T]TGTCTTATAGGAATT | 57626 |
rs182371688 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866171 | ACTTATGCTGAATTG[C/T]GGCAAATTGAGAAGT | 57626 |
rs182374677 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806780 | TTTGAGCCTGGAGTA[A/T]CCTCAGTGGGAAGCC | 57626 |
rs182377439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828394 | GTAGGCACTCTCAGT[A/G]CCCAGAGAAACCATT | 57626 |
rs182384542 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704905 | TCAATATATCATTAT[C/G]AATATATCTTATATA | 57626 |
rs182387240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729916 | TCTGATATTTTTTAC[A/G]AAGAAAGATACTAGA | 57626 |
rs182389137 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69902424 | TATCATGGTATACTT[A/G]AAGAGTATTTTCAGT | 57626 |
rs182391436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773616 | TTGTGCACCCTCTAA[A/C]TCCTACATTATTAGG | 57626 |
rs182396273 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948760 | ATCATCCCCTATTAA[C/T]AAATGCACAGAGTAT | 57626 |
rs182398059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884077 | AGTGACCATTAATCT[C/G]TATGTTAGAGCAGTT | 57626 |
rs182398760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723267 | CTATTGCACATTAGA[A/G]TGACTACGACTAACA | 57626 |
rs182404971 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69941963 | ATTGAAACAGTAATT[A/T]AAAAAACTCCCCCAA | 57626 |
rs182406802 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69981488 | TCTTACATACATAGA[A/T]CTTAGACAAAGACCT | 57626 |
rs182408506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745049 | CTTTCCAGGTTTTTT[C/T]TTTAACCAATTTTTA | 57626 |
rs182413076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966394 | GGACGACAGCACATC[A/G]TTTGCAGAATGGCTT | 57626 |
rs182414399 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921837 | AAGAACAAGGTTATA[C/T]AAAAGCATAGTAATA | 57626 |
rs182414612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997952 | GATCCTGATTTCAAT[C/T]CTTTTGGATATATAC | 57626 |
rs182415088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748608 | GACCATATCACCACC[A/G]GTATGACATCAGAGA | 57626 |
rs182425740 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872304 | TAAACATGAGCAATC[A/G]GCCTGTTTTACAGCC | 57626 |
rs182426098 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018583 | ATGACTGTGCTGTTT[A/G]GTGAGACTGAAAGCA | 57626 |
rs182434958 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037868 | AGTATTTTTTGACAG[A/C]CTCATATTTCTTCAT | 57626 |
rs182437913 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70056063 | ACAATCAAACATACA[A/T]AACTAGAACCAACAA | 57626 |
rs182443286 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69784921 | TTGAGACAGAGTCTC[A/G]CTCTGTCGCCCAGGC | 57626 |
rs182444389 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911293 | CAGTAATTTCTGCAT[A/C/G]TTGGGAGAAAATCAA | 57626 |
rs182459734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765969 | TCAGTTGACTAACAG[A/T]TTCTAACAGATTCAG | 57626 |
rs182460427 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708947 | AATGAAGAAATAAAA[A/G]TACCTATACTTTGCT | 57626 |
rs182462302 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947883 | AAAAAAGCATGAAAA[C/G]TGCTAATGGAAAGAA | 57626 |
rs182493251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980430 | ACACATTATAAGTGC[C/T]TGTATGATCTGATGC | 57626 |
rs182509943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849924 | AATATCACATCTCAA[A/T]TTCAATGCATACGTT | 57626 |
rs182525369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815562 | TTCCAAAACTGGGGA[G/T]GGAGGAAAGTGGGAA | 57626 |
rs182532689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888285 | ATTAGGTTTTAACAT[A/T]TGGAATTTGGGGGGA | 57626 |
rs182544708 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69916782 | AAACCACATAGTAAA[C/T]GGCTATATTTACGAC | 57626 |
rs182548519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045620 | TTTGGACTTCTAAAG[A/T]TGACTGGTAGTAGTA | 57626 |
rs182560329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952283 | GGCATATGTTTCCAA[A/G]TAGTATTTACGTTTT | 57626 |
rs182573062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849129 | ATCAAATATTTAGTC[A/C]GTGCTTATTTTGTCC | 57626 |
rs182585473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832711 | ACTTCAAACTGTACA[A/C]TAAGACTATAGCCAC | 57626 |
rs182602661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908403 | GAGAGAAGATTTGAC[A/G]AAAAAAGTTCCTGAA | 57626 |
rs182612734 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870818 | GTAACTCTATGTCCG[C/G]CACCTGGGGCACACT | 57626 |
rs182616318 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887789 | GAGACTTTCTCTGCT[G/T]CTCTCTTCTGAAGTC | 57626 |
rs182621928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944695 | TCCCAGTAGACTTTC[C/T]GTGAAAATTGCAAAA | 57626 |
rs182622629 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70102065 | TTAGTTTCATAGAAG[A/T]ATAGTTTGAGAACCA | 57626 |
rs182629397 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084170 | CAATCATGAGGAAGG[C/T]ACTTTAAATTATACA | 57626 |
rs182629864 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69924349 | TGCCCATGGCTGTCC[A/C]TGAAGCAATCAGCAT | 57626 |
rs182646485 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708444 | TTGATTCCCTGGGTA[A/G]GAAGGTACTTTCAGT | 57626 |
rs182652704 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726758 | CAACCTTAATCCCTC[A/C]GTGTTTCCTCTGCTC | 57626 |
rs182691867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769924 | TTGCCAAGCTGTGGG[C/T]GGTGACATGCTCCTG | 57626 |
rs182700738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770562 | TAGTCTGGTCTTGGG[C/T]TCCTGGCCTCAGGCA | 57626 |
rs182701828 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748317 | AAAGAGGTTTAATTT[G/T]ACTTTCAGTTGCACA | 57626 |
rs182711270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727132 | AGGGTTCATAGGAAA[A/G]GTACAGATTAAACTA | 57626 |
rs182721982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800187 | TTTCTCTGACATTGA[A/C]CCTTGTGATTACAAT | 57626 |
rs182731530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797737 | AGGAGGCTGAGGCAG[A/G]AGAATGGCATGAACC | 57626 |
rs182754444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715473 | TGGAGCTATGAGTCA[A/G]TTATACCTCTTTTCT | 57626 |
rs182757616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835146 | AGACAAAATACCTAC[A/G]TTTCAAAAATTATAG | 57626 |
rs182759472 | snp | A/C/T | 0.00573975 | 0.0532628 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734499 | TTCTGAATTTAAAGA[A/C/T]GAGTAAGTAGAACTA | 57626 |
rs182765150 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833292 | CATCAAAAAGTGGGC[A/T]AAGGACATGAATGGA | 57626 |
rs182768585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753228 | GAACCCAAACCTTCA[C/T]AGCTGTTAAAATAAA | 57626 |
rs182793364 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873548 | GCTCTAATAACTCTT[G/T]ACAGCAGGGTTCTTA | 57626 |
rs182798661 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809823 | CATCTGATGTGTAAT[A/G]AGAGCCATAGGTTCA | 57626 |
rs182800233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909297 | ACTTACAGATGCAGA[A/G]AGGATGTATGCCAAA | 57626 |
rs182800705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971180 | ATGCCTCCGTTTTCT[A/G]TATTATAGAGAAAAG | 57626 |
rs182809295 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69913076 | TCCACAAACTGGAGT[A/T]CCAGGTGCTTCCCCA | 57626 |
rs182810395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791549 | TACTACAAAGCTTCA[A/G]TAAACAAGAAAATGT | 57626 |
rs182815681 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69986576 | ATTTAGAAAACTATG[A/C/T]GAATTACATTCTGCT | 57626 |
rs182817490 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936507 | GACAGGAGAATTGCC[C/T]GAACCTGGGAGGCGG | 57626 |
rs182821170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004204 | GTCAGTCCTGAAAGG[C/T]TGGAAATAGAGCCAA | 57626 |
rs182821860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871080 | GCTTTCTGATACATC[C/T]TCTGAAATCTAGGTG | 57626 |
rs182822072 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776964 | TGATATAGTTTGGCT[A/T]TGTCCCCACCCAAAT | 57626 |
rs182826111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024435 | ATGAGTGTTTTTCAC[C/T]AGGATAAAATCGAGT | 57626 |
rs182829543 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043342 | AGTGTTATTACTAAG[A/G]AGTCAAAATGCTAAA | 57626 |
rs182832001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970207 | GTTGTAAACATAACC[C/T]TGTATCTCAAATGCC | 57626 |
rs182841033 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827686 | CAGTGAGCCAAGATC[A/G/T]TGCCACTGCACTCCA | 57626 |
rs182842922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061910 | GGGTCATCAGCATGT[A/G]TATCAACTCAAACAT | 57626 |
rs182848159 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099101 | AATATTAAAAATATG[A/G]AATTTTACTTACACT | 57626 |
rs182849816 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70077872 | ATGAAAAACCTCTGG[A/G]TATGTTCTGTGCCCT | 57626 |
rs182850142 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974724 | AAGAATAGCTCTTAC[A/G]CTGAAGAATATAATT | 57626 |
rs182860968 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105295 | CTAAACTGTTTGTTC[C/T]GTTATTAGTTTTAAT | 57626 |
rs182870242 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008082 | GAGTATCACAGTATA[C/T]ACTTTTTACAAGATT | 57626 |
rs182895521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047505 | TTCTTTAGAGACACA[C/T]TACTTACCCCACTCA | 57626 |
rs182902519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070273 | GCAAATAAGATAAAC[A/G]TCAAGATTCTTCACC | 57626 |
rs182909084 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70093318 | CATCTGCAAGTTTTC[A/G]TACCTCCTCTGATAC | 57626 |
rs182926443 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098076 | GCTTGTCACATGCTG[C/T]AAGCATTTTCTATCT | 57626 |
rs182971772 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718478 | TGAATGAGGAAAAAA[A/G]GCATCATGGTATTAA | 57626 |
rs182982901 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737575 | CAAGACTGGGCGGTC[C/T]GGACTGGGAGCAAAC | 57626 |
rs182984930 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709877 | TTGGCAGAAAATTTT[C/T]CTAGTACAAATAACT | 57626 |
rs182988843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758287 | TACAAAAGCTAATTT[C/T]AATAATCCTATAAAC | 57626 |
rs182994422 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714061 | TTGATATTCTCCCAA[C/G]TTTTTAAATCCCCTC | 57626 |
rs183013487 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813408 | CAGCACACCAACATG[A/T]CACATGTATACATAT | 57626 |
rs183029731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796131 | ACTCTTTTAGAGAAC[G/T]TTAATATGTATCTCA | 57626 |
rs183033039 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931836 | TATGTTACCTGTTAA[A/G]AAGTTTTGAAATAAA | 57626 |
rs183035577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820940 | TGTTTTCTTGGAAAG[A/G]GCAATAGTAAAAGTC | 57626 |
rs183038484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727613 | AAACCACTGTATTCT[A/C]GAATGAAGAACCTGG | 57626 |
rs183040417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797178 | CACAAATGTTCACCT[A/T]GTTCGAATTACATAA | 57626 |
rs183040537 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719262 | AATGTATCTCTAGGT[A/G]TTGAATTTACCCTTC | 57626 |
rs183041619 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848225 | ACATACAGAGAGAAA[A/C]ATGGACAATTATGCT | 57626 |
rs183044394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949401 | GATTGATATTTTGCT[G/T]ATTATTAGACTGGGG | 57626 |
rs183047697 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990529 | TGTAATCCTAATTTC[A/G]AGCACAAAAGACTTT | 57626 |
rs183050370 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982208 | GGAGGCCAAGGCGGG[C/T]GGATTACCTGAGTTC | 57626 |
rs183050716 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007713 | TTCCTAGTACTGTAT[C/T]ACTTTACAAATTAAA | 57626 |
rs183053183 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759632 | ACAGATAGTCTGAAT[A/G]TGGAAAAGAAAACTA | 57626 |
rs183055231 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70029391 | TTGATGAAGGTGAAG[C/G]CTGATATTTGAAATT | 57626 |
rs183055394 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967281 | ACCATTAAGTACATT[A/C]ATAAGTCATGGGAGG | 57626 |
rs183062104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832106 | CTAGCCAGAACAATC[A/G]GACAAAAGAAAGAAA | 57626 |
rs183063743 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046519 | TTGAGACAGAATCTC[A/G]CTCTGTTGCCCAGGC | 57626 |
rs183065706 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69891765 | ATTTGCAATTATTTT[C/G]GGAAGATTCTTTAAC | 57626 |
rs183070439 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066834 | GATGAAAGTGGCCAA[A/G]TTTTATCATAACAGA | 57626 |
rs183080599 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69854593 | TCTTGGCAAACTGCA[A/G]TAATTAGATAAACAG | 57626 |
rs183087178 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102510 | CAATCTCCACCAAGG[A/G]AAAAAGAAAATTATT | 57626 |
rs183088592 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69930085 | TTCACATCTCTTTTG[C/T]CTAGGTTTCCAAAGA | 57626 |
rs183093674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085238 | CAGAGAGAGAGAGAA[C/T]GGGAAGTGAGGAAAA | 57626 |
rs183122609 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961674 | CTTGAACGATATTTT[C/G]TCTTTCACATTTAGG | 57626 |
rs183144589 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957761 | CTCTCTTTACAAATG[C/G]CTAAGATCACAAGCA | 57626 |
rs183147647 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69994047 | TTGGGATTGAGAATG[C/T]ACAAAGGACTAATGA | 57626 |
rs183152344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991186 | TTATAGTACTAAACA[C/T]CCATATATAAAAGTT | 57626 |
rs183161834 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033500 | TTTTAGTAGAGATGG[C/G]GTTTCACTGTGTTAG | 57626 |
rs183162764 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014807 | AACAGATAAACAGAC[A/G/T]CTTGCTTTTGTGGGA | 57626 |
rs183167581 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034747 | ACCATCGTTCTTTTC[G/T]CCAGACATACATATA | 57626 |
rs183171933 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053138 | GAAATTTAAGTGTAG[C/T]CTTAAAAGAAACATA | 57626 |
rs183172340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029438 | GCCAGAAAAGAGTGG[A/G]GGCCAATATTCAACA | 57626 |
rs183179080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070547 | TAAGGAAAAATAAAA[A/C]AATTCTTAAACAAAA | 57626 |
rs183187355 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110418 | CATGAAGTTATGTTA[A/C]ACTGAAATGACTGAC | 57626 |
rs183190625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067673 | AACAAAAAGGTTCTT[C/G]ATGTGGCTTTGAATT | 57626 |
rs183199970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069419 | CTTTTAACTGATAAA[C/T]CATGTATGTCTTTTA | 57626 |
rs183213452 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714716 | CTCCCACCTCAGCCT[C/T]CCAAGTAGCTGAGGC | 57626 |
rs183218049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878237 | ACACTATCCTGGAAA[C/G]ATCTGTTTTTTTTTA | 57626 |
rs183231224 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916942 | AAAAAGAAAAACGTG[A/C]AGAAGAGTGTGTAGG | 57626 |
rs183249921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936771 | TCAGGGAAGTTTCTA[C/T]TGAAGATTTCAACCT | 57626 |
rs183250481 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700239 | TAATATTTTCCTTGG[A/T]TGTTAGATTTCAAAT | 57626 |
rs183251162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896194 | ATGGCAGGTTGAATT[C/T]TTCTCATGATTGGAA | 57626 |
rs183260392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952807 | TCTTCATTAAAAATG[A/G]CTAAGTGGTAATTTA | 57626 |
rs183268815 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985654 | GCCCAAAGGAAATGA[A/G]ATGAATATGTTGAAA | 57626 |
rs183268900 | snp | A/G | 0 | 0 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970940 | TAGTCTTCATTTCAT[A/G]CCTGGATTAACCAAA | 57626 |
rs183269467 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733178 | CTAATATAAACACAG[G/T]AAAAACATCTATAAG | 57626 |
rs183300602 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099795 | CTAATGAACAGCTTT[C/T]GTTAAACTAAGGTTT | 57626 |
rs183309110 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781456 | AAAACCTTTGCCTGT[C/T]GGAAGTTTGAAGCAT | 57626 |
rs183309201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738735 | TCAACAAAACCTCTG[A/G]GAACTATGAGACTGT | 57626 |
rs183311908 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704750 | TATACATTTTTAAAA[A/G]TCTGCCTTTGTTCTC | 57626 |
rs183322629 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744340 | CCAACTGCATATTTC[C/T]GTAGGATTTGAAAAT | 57626 |
rs183342141 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814551 | CTTAAAAAAAATCAA[C/G]AAGTAAAGTTAAAAA | 57626 |
rs183349095 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820265 | AAGTAACACCAGTCC[C/T]CCATAACAGGGTTCA | 57626 |
rs183372104 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844364 | GAATAAAATATTGTG[C/T]AAAATGTAACTTTGG | 57626 |
rs183375269 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917283 | CTTAAAACCAAAAGG[G/T]ATTCCTAAAAACTGA | 57626 |
rs183383921 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69879420 | AATTCCACATATTCT[A/G]TCTTCTCTTGGTAGC | 57626 |
rs183385310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921121 | CCAGTAGAGAGTTAA[A/G]CAGAGTTGCAATTAT | 57626 |
rs183395624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953414 | GCTGCCTCTCATATT[A/G]AGCAGACAGAATGTT | 57626 |
rs183401849 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883320 | TCTCTTTGTTTTTCA[A/G]CTTGCCATCTTGTTT | 57626 |
rs183404059 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69767030 | ATATCAAAGTAGCAA[C/T]TGGTATTTTTCTAGA | 57626 |
rs183404777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977054 | CTGATTTCATTAAGC[G/T]GAACTTTTAATTGAA | 57626 |
rs183415622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013137 | CTGGCACTCTATTTA[C/T]TTAGAAGGAAATGAA | 57626 |
rs183417414 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835563 | TGGCTCTAAGTTACT[A/G]AGGCCTTTGGTTCTG | 57626 |
rs183427691 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038023 | GCTCTCATTTTCTAC[C/G/T]GCTTTGTAATTACAC | 57626 |
rs183429604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955827 | AATATTTGCTGTTAT[C/G]AAAAATTGTTTTGCT | 57626 |
rs183430191 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052081 | TTTACTTTCTTAGCC[A/G]TGCAATAGGCCATTG | 57626 |
rs183435478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057284 | AATGAGATTGGGGCT[A/G]TAATAAAATGTTTCC | 57626 |
rs183443134 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073168 | CAACCCAAATGTCCA[A/C/T]CAATGATAGACTGGA | 57626 |
rs183443318 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821410 | ACCTCCACCTCCCAG[G/T]TTCAAGCAATTCTCA | 57626 |
rs183453518 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110281 | TATAGGTACCTTTCT[A/G]TATTTGTCAATCTTA | 57626 |
rs183455262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801019 | CTACAAGGTGAAGTC[A/G]AATTACTCTGTGCGT | 57626 |
rs183459541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920749 | TCAAAGAAGTTTTCC[A/G]TTCACAATTGCTCTT | 57626 |
rs183460983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873778 | ATTTAAAAAAGTAAA[C/T]GAAGCTAAACTTGCT | 57626 |
rs183466764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892640 | TCCAGGAACTAAAGA[A/G]TTTTATTGTCAACCT | 57626 |
rs183471196 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855287 | ATCACTCGTACTAAT[A/T]TTAGATAGATAGATA | 57626 |
rs183477801 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900306 | GGTCTCACCATATAG[A/C]TCATGAAACTTCACG | 57626 |
rs183479790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088130 | ACTTCTAAGTAAATA[A/G]TGAGCGCCACGAACT | 57626 |
rs183480844 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019880 | TTTTGGGAGGTGTTT[A/G]GGTCATGAAGGCTCC | 57626 |
rs183493040 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057897 | GAGCAAACCAAATTT[A/G]ACAACACATTAAAAT | 57626 |
rs183502363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940373 | AGATAAATATAACTC[A/G]GTAAAGGTCACCAAT | 57626 |
rs183550131 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799574 | CATCTTCATTTTTCA[A/G]ATTAGAATTTATATT | 57626 |
rs183555611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722758 | AAACAGTTTTTTGAG[G/T]GTAGTCCCTCAAAAA | 57626 |
rs183566533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765542 | CTTATCTTTAATTCC[C/T]ACAATGTCCGTGTCA | 57626 |
rs183569500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806561 | AGCTGGGAACAGACT[C/G]ACAGCTGGAAACCAA | 57626 |
rs183588024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841538 | GAAAATTACAAAACA[C/G]TAATGAAAGAAATTG | 57626 |
rs183589651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862178 | AACTTTGTTAGAGAA[A/G]CAAATTACACATATA | 57626 |
rs183591861 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772108 | AGGCGCCTGCCACCA[A/C]GCCCAGCTAATTTTT | 57626 |
rs183596945 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69865670 | GAAAGTGGAGATTTA[A/G]AACATTTTAAAGGTG | 57626 |
rs183601656 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825284 | ATAAAAGAAGAAAGA[A/C]ATCAAGCATAAAGCA | 57626 |
rs183602954 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897045 | ATTTGATCAATAGAA[C/T]AGTATTGATAATATT | 57626 |
rs183611593 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917428 | TTTTAAACTGCCTAT[A/T]AAACTGACCTAGAAT | 57626 |
rs183614225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879936 | AATCGTTTGGTAACT[A/G]AAGAAATAAATGAAT | 57626 |
rs183616618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059550 | ATCATATTGAGTTAA[A/G]ATGTTTTTGCACAGC | 57626 |
rs183621820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074478 | ATCTCACTCATATCC[C/T]ACCACTGATTGATTA | 57626 |
rs183623910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869728 | AATGAAAATCTTAGT[A/C]GTAACTGTTTCAACA | 57626 |
rs183632426 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804190 | TCATGACAAAACGAA[C/T]GGTAGACTCCTTTCT | 57626 |
rs183640289 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901890 | GCAACCTCTGCCTCA[C/T]GGGTTCAAGCGATTC | 57626 |
rs183651789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840506 | TGGGATTACAGGTGT[G/T]AGCCACTGTGCCTGG | 57626 |
rs183652846 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700640 | TAATTAAAATTTACA[A/T]GGGCCTATTTATTAA | 57626 |
rs183654517 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941087 | TGTATAACAATGAAC[C/T]TAAACTATACCCTAA | 57626 |
rs183664137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719794 | AGTATACTAGATGAA[A/G]TTAAGACAACTATAA | 57626 |
rs183665406 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974226 | CTTAAGAAACACATC[A/G]ATGATTGATAATAAT | 57626 |
rs183672747 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739481 | TAGAGTCAAGATTCA[C/T]TGGTGTGCTGTATTC | 57626 |
rs183703909 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998462 | TGTGACCCCATTAAC[A/T]GACTATGGCTCACAT | 57626 |
rs183720299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038477 | ATTTTTTAAGAAACT[C/G]CCAAATTATTTTCCA | 57626 |
rs183734312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003376 | GATTCCTATAGAGAT[A/G]TGTGGAGTTTAGAGG | 57626 |
rs183737581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073522 | TGTAACAAGCCTGCA[C/T]GTTGTGCACATGTAC | 57626 |
rs183757587 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724490 | CACTTCTGAACACAC[C/T]CTGTGAGGTCAGCAT | 57626 |
rs183764316 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746587 | TTTTAATATTTTCTT[A/G]CTTGTTTAATCAGTT | 57626 |
rs183775694 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69810343 | TATATGAAGCATCTC[C/T]TTGGATCACAGTGGA | 57626 |
rs183775716 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767553 | ATAAAACTTTTAAAA[A/G]CAGTAAATATCGGTC | 57626 |
rs183777352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042844 | GTCATTGCCCCTGAA[G/T]ACTCTCCAGTGGGAC | 57626 |
rs183784415 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108699 | TGCTTTTGCATCAGT[A/C]AACACCACACATGAA | 57626 |
rs183788672 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091953 | ATCTTCTGCCTGGCA[A/G]CAGGGTGTAGTGGGG | 57626 |
rs183789223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077653 | CTATATCAAAATGAT[A/G]TGTTAATAATAGGGG | 57626 |
rs183801368 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706720 | AAATAATAGAAATAT[A/T]GAGAGATTTGGAGAA | 57626 |
rs183806874 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088823 | TGTACATATGAAAAA[G/T]AACATTTTTCCCTTA | 57626 |
rs183808481 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69801739 | TGTCCAATTTTATAA[A/C]CTTGATAATTTATTA | 57626 |
rs183817837 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785683 | TGAAGGAAATAGAGA[A/C]ACAAAAAACCCTTCA | 57626 |
rs183822166 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947476 | ACATATTTATTCAGT[A/C]TAAATTCAAACCCTT | 57626 |
rs183832131 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69980037 | GTCTTTGTTGTGGCT[A/G]TCTTTAGCATTTAAT | 57626 |
rs183834872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964938 | AGTAAAATTTGATTA[C/T]ATAACAGATACTATA | 57626 |
rs183835786 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824846 | ACATACCTGTATGCA[A/T]TGTGAAAACTCACTT | 57626 |
rs183840808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995288 | AGAGTGTTGATTTAC[C/G]TGTGTATATACAACT | 57626 |
rs183846543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749156 | TAGGTAGGGTGAATA[A/C]TTGGACTAGAATAAT | 57626 |
rs183855443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016869 | ATGGCCACCCATGGA[C/T]AAATCAGCATGTACT | 57626 |
rs183857513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788678 | ATAATAATAGAAAAT[A/G]TAGTATTTATGTATA | 57626 |
rs183862540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860685 | ATATTTAAAAATATT[C/T]TGTACATGTTTAAAT | 57626 |
rs183865071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078342 | CATCCACAAAAATAA[A/G]GTATTTTGAATTACA | 57626 |
rs183866987 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035609 | AAAGTTTGGAAAGAC[A/T]TGGATAAAACAACCA | 57626 |
rs183869857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887386 | TTGGTGTTCTCTATC[A/G]AGCAGCTTTTTCATT | 57626 |
rs183871501 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054665 | CCAAACAAAATTCAA[C/G]ATAACCCAGAGAAGG | 57626 |
rs183877979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071523 | AACAGCAGAATATGC[A/G]ATCTTCTCAAGCTCA | 57626 |
rs183891015 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103596 | TAGCTTAGATTAGGC[A/G]CAGACAATGGCTGTG | 57626 |
rs183899780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086082 | TACTATTCCCATCTT[A/G]TCTAATGGAAATGTA | 57626 |
rs183916618 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69827556 | CCAACATGGTGAAAC[C/T]CCGTCTCTACAGAAA | 57626 |
rs183924668 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752483 | TGATTTCATGTGGTA[C/T]GTAGACATTGTTTTA | 57626 |
rs183930932 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69723454 | ATATGTAGAATTATT[A/G]TGTGTCAATAACAAA | 57626 |
rs183937121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864679 | AAATCTAACTATACA[C/T]TGATAAGCAATTGTT | 57626 |
rs183941271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023722 | AAAATCTCACAATAT[A/G]GCTTTGTTTGACTGC | 57626 |
rs183944322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994671 | TTAAGGTTGAACTGG[C/G]TGAAATGAATTGGTA | 57626 |
rs183962342 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70061681 | TAAAAATTAGCAGCA[A/G]ATATGAAGGCTTATC | 57626 |
rs183987141 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105755 | CTTTTAATAACATTT[G/T]ATAACTTCATAGTAT | 57626 |
rs183997128 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749461 | ACATATAATTATTTA[C/T]AATTTTTGGACTGTA | 57626 |
rs183998593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69702318 | TGACAATCACTGAAA[C/T]GAGAACTGAGTATTT | 57626 |
rs184015105 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772880 | TTTGATAAATATAAA[C/T]AAAGCACTAGAGTGT | 57626 |
rs184019095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930758 | TGATCTGTGGAAAGT[A/G]TGGATTTTTAAAACA | 57626 |
rs184025628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966739 | TGTACCCATTAATCA[C/T]TTTTTCACCTTCCTT | 57626 |
rs184027905 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711037 | GTCACAGAATAAAAG[G/T]TAATTTCTCTTTGTA | 57626 |
rs184045996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805050 | TTTAGTATAACATTT[G/T]TATACTTATATAAAA | 57626 |
rs184051778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943429 | GAAGGAAAAAGAAGA[A/G]CAGATACACTGCAGA | 57626 |
rs184052115 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789274 | AATTATTTTACATGT[C/G]TGTCTGTCTTTTATT | 57626 |
rs184053729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745811 | ATTAATATCCTTTTG[G/T]TATTTCATATGAATT | 57626 |
rs184055967 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998360 | CAATGGGAGCTCCCA[C/T]TGTGTGGGAGCACAA | 57626 |
rs184061538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922421 | GTATTAACAGGGAAA[G/T]GTGATCACATAACTG | 57626 |
rs184064969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967458 | TGTAACTGAATTGCC[A/G]CAATGTCATGATCAA | 57626 |
rs184075739 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959775 | CTAACTTGGGTGAAC[A/G]AATTGCTTCAAGTTG | 57626 |
rs184076063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824991 | ATTCATGTTTTCAAT[C/T]TTGAAATGCATTAAA | 57626 |
rs184076690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983426 | AAGTAAACTAGCTGG[A/G]GGCATTACACTACCT | 57626 |
rs184078802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000649 | AGAATATATAGCTAA[C/T]ATATTTGTCTACTAA | 57626 |
rs184082671 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70102872 | TATCAAATATTTATT[A/C]ATTTGACAGTATTTA | 57626 |
rs184083697 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69705206 | TCTTTATGTCTTGAA[A/G]CACGTGCATTATTTT | 57626 |
rs184083916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809724 | TATAAACAGTCTAAA[A/C]ACTCGATTTAAAAGA | 57626 |
rs184089653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021008 | ATACATTCACTATAA[C/T]TGGTGAAACTATGTT | 57626 |
rs184100644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039362 | GTGCTGGGATTACAG[C/G]AATGAGTCACCAGAC | 57626 |
rs184103746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058931 | AGTGAACTCATTATT[A/G]TCAAAGGTGCCGATA | 57626 |
rs184108517 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881963 | TAGGCTTTTTACATA[C/T]ATATTATCTAATGGA | 57626 |
rs184111688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074181 | TCAGCATGATTTGAA[G/T]AATTAAGAGATTTGG | 57626 |
rs184120154 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69843691 | TAAAAATGATTTAGG[A/G]TGGCCAAAGTACAAG | 57626 |
rs184121103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040517 | CTCTCTTTAGGCACT[G/T]GAAAACTATTGTGCT | 57626 |
rs184125283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100487 | AGATATGACAAACTT[G/T]TATTCAAATAAAAAG | 57626 |
rs184164801 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949096 | TATAACTGTTTCCCC[A/C]ATTATTAACATCTTA | 57626 |
rs184167093 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69988829 | TTTGTGTGTGTGTTT[A/T]TGTTCCTTATAGATT | 57626 |
rs184169237 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69914498 | AAGGCAACAAAATAC[A/G]ACAAGCTTAGAGAAA | 57626 |
rs184171626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005988 | TTCCTAAAACTTTAC[C/T]TCTATTTAGCAACGA | 57626 |
rs184173197 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027843 | GAAATATTTAGAATT[C/G]GTTCTGGAGCCACTC | 57626 |
rs184186007 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044880 | GCACACCAGGAGTTA[C/T]AGAACTGAACTGGAT | 57626 |
rs184192653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063964 | TAATTCAAAATTAAC[C/T]AAAACATCAAAATTA | 57626 |
rs184193297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981881 | ACTGTAATTATGATA[A/G]ATAAACCACATATAT | 57626 |
rs184197989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081393 | TCAAGATTTTGGGTC[C/T]ACTGCTTTTTCATCT | 57626 |
rs184209916 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70019503 | GAGGGCAGAGGCTTT[A/G]GTCAAAGAACAATAG | 57626 |
rs184223558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706285 | TCTTTTTACTTACTT[G/T]GCTAAATGTACCTAT | 57626 |
rs184239153 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085989 | CTTTACTTCTCGTTA[A/C]GTATGTTTTAAATTA | 57626 |
rs184241247 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047971 | ACAAGACAGAACTAT[G/T]TAAATAAGTCATTGA | 57626 |
rs184252902 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69712320 | TTTATTGTTTTATGG[A/G]TAATATTTAAATCTA | 57626 |
rs184262721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789493 | AATTTAGTTGACTAC[A/T]TTTTTCATCACTTTT | 57626 |
rs184268324 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69871429 | AGTCACGCTAATTTC[C/T]CTAGTAAGCGATTGC | 57626 |
rs184283303 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850942 | TGACTCCTAGTTTTA[C/T]CCTGTGTTTCTAAAT | 57626 |
rs184293123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750622 | TATAAATTTCTATAT[C/T]TGTGTAAGTACTATG | 57626 |
rs184297399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889191 | ATATTGCTGTCAAGA[G/T]TCTAACTTTCTCAGG | 57626 |
rs184301037 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927850 | TCTCAGAATGTTAAA[A/C]ATGGAGTTATTGTAT | 57626 |
rs184302807 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910147 | TTCCTTATGTTTGCA[C/T]AACACTTGGCATATG | 57626 |
rs184312266 | snp | A/C/T | 0.0047834 | 0.0487097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964844 | AATACTTTAAACAAC[A/C/T]GGGTCATCTCTTGGT | 57626 |
rs184317030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947330 | AATTGACCATTTATA[C/T]TGGAAAAGTATATTA | 57626 |
rs184331562 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852189 | TTTAATGGTCATCCT[C/T]AAGCATAGCTTCCTT | 57626 |
rs184356414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103936 | GATGCAAATCTGTAA[A/T]GACAGTTTATGGATG | 57626 |
rs184368272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889757 | TGTATGTAAATGAGG[A/G]TGAAAATAGCATCCA | 57626 |
rs184369797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953637 | CATGAATATACAATA[A/G]AAATCCATCTCAAAT | 57626 |
rs184374265 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69988024 | GGCGAACTCATGACT[C/T]GAGGGTTTTGTGTAC | 57626 |
rs184383039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009800 | ATTTATTGCCAATTT[A/G]GATCCATAGTAATAA | 57626 |
rs184400180 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:70049642 | TTTTATAATTTATGA[C/T]GCATTTTAATATACA | 57626 |
rs184401243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025560 | GAAAGTTGTTTCCCC[A/C]AAAGTATTTGTATTA | 57626 |
rs184404694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729490 | GTTAGAATGACACAT[A/T]AGTGTTACGTGATAG | 57626 |
rs184407148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068298 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 57626 |
rs184415429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062670 | GAGTGAGTAAATATC[A/G]TACCTGTCCATGCCT | 57626 |
rs184417465 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773111 | GGTGTGCAATGTCCT[C/T]TAATGGAAGCATTTG | 57626 |
rs184445895 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755658 | AATTTTAAAAAAAAA[C/G]CACTGCAGAAAAAAG | 57626 |
rs184458883 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872009 | CAACACTGACTCTCC[A/C/G]TATCAATTTTCTGCC | 57626 |
rs184462756 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69794683 | AACAGAGATAAGGGA[G/T]AGTATGAAAACCACT | 57626 |
rs184468626 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778646 | AATGAGTAACAGGTT[A/G]GGTAAAAGCTTGATT | 57626 |
rs184478061 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910715 | TTTTCACTGGATAGA[C/T]GTGATAAAGCCCAAT | 57626 |
rs184482436 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938111 | TGCCTGATTGGACAA[A/G]GATCAGAGGCAAATA | 57626 |
rs184485028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735687 | AGTAATTTTAAAAGA[A/T]AAAAGTACAACTATC | 57626 |
rs184492719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971925 | TGCTGACAATCTACT[A/G]TAGACATAAGCAAAA | 57626 |
rs184495178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829940 | AGCACTACAAGAACT[A/G]CTAAAAGGAGTTCTA | 57626 |
rs184495203 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874749 | ACCAACTTAATTTGG[A/T]TAACCCTGACTTCCT | 57626 |
rs184497382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811113 | GGCCTCCTCCCTAAC[C/T]CATTTTGGGAAACCC | 57626 |
rs184506070 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855715 | AAGTTTCCTGAGGCC[C/T]CACCAGCCATGCCGA | 57626 |
rs184508527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100234 | GGTCTTTCAGTGTAT[A/G]AGTCTTTCACATCTT | 57626 |
rs184514511 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70004956 | TATCTACAAATATTA[C/T]AAGTAATTTTAATTA | 57626 |
rs184523154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893058 | CCTATTTTTGAAGCT[C/T]TTCTGAACAGTAGAA | 57626 |
rs184527945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845766 | AAAATATCTTGAAAT[C/T]ATGTGGAGCATCAAG | 57626 |
rs184529772 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867329 | TTATCTTCCAATAAA[A/C]CCTCTCTTCTAATTT | 57626 |
rs184533760 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69914899 | TTAAAATTAGGTGTA[A/G]ATGGTACTAACCTTA | 57626 |
rs184536643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043517 | CTCACTACTTACTCA[C/T]TGACTCATCCAGAGC | 57626 |
rs184539175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734810 | ATATTAAAGGTACTA[C/T]ATATAATAGTGTCCA | 57626 |
rs184543415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777495 | GCAAAAGGATATTTT[C/T]CATATTTTAAAATAC | 57626 |
rs184571297 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897990 | TCCTCACCATGGAAA[A/G]AGTAGTCATGGTCAA | 57626 |
rs184581525 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875857 | GTAATCCTATTCTTT[C/T]TTTTTTCTTACTCCT | 57626 |
rs184585748 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837626 | TCTCTATATATATGT[A/G]TGTGTATATATATAT | 57626 |
rs184588276 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939284 | ACAATTGAAATGGCT[C/T]TTAGATTCTCTACAA | 57626 |
rs184600093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918049 | TCAAAAAGGCCAAAT[A/C]ACTTGCAGAATTTAC | 57626 |
rs184602005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954460 | AAGGAAAATGAAAAC[A/C]ATTATAAGACTGAGA | 57626 |
rs184621293 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69972630 | CTTCAACACTGTTTC[A/G]ATGAACATAAAATGA | 57626 |
rs184628046 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988357 | ATTGTCTTTATCCAG[C/T]CTATGGTTGTTTGGC | 57626 |
rs184629834 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949487 | ACTTATCACTGGTGA[C/T]AGTCATCTTGATCAC | 57626 |
rs184630694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005424 | GCTTAGAACGTGGCC[C/T]AACACAAATTCATGC | 57626 |
rs184635762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096204 | TTCCTTTTGGATATA[A/T]ACCCAGTAGAGGGAT | 57626 |
rs184636626 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026608 | AAAATAAGACAACAT[A/G/T]TATTTATAAGGCTAC | 57626 |
rs184660028 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715795 | CAGCAATAATATATC[A/G/T]AATGAGAAAAGGTTT | 57626 |
rs184669834 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792721 | AACGGAATGAAATAT[A/C/T]GATATACACTACCTG | 57626 |
rs184673410 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976043 | AAAGAGGTTTAAAAA[G/T]ATGTTGTCTGTATTG | 57626 |
rs184679520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753920 | CAGTTCACTGCATCC[C/T]TGACCTCCCAGGCTC | 57626 |
rs184682802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011357 | AATAAAATATGATTA[A/G]TATAGAAAGTTTAGT | 57626 |
rs184698425 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050151 | TTTTATAATATTCAT[A/G]TTAGTAATTTAATTC | 57626 |
rs184702994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751086 | CTCTACAAGCCTCTA[A/G]TATCTTTCATTCATG | 57626 |
rs184708982 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782363 | CGAAGCAGGGCAAGG[C/T]ATTGCCTCACTCGGG | 57626 |
rs184711874 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856266 | CCATTCTAAAATATT[C/T]AGGTTCTCTAAGCTC | 57626 |
rs184716154 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761416 | TCCAGTTAGGTTACA[G/T]TTTACTAGGTATGAT | 57626 |
rs184722073 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69782811 | CAGCTTTGAAGAGAG[C/T]AGTGGTTCTCCCAGC | 57626 |
rs184723193 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833764 | ATATATATATATATA[C/T]ATACATACATACATA | 57626 |
rs184738359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816751 | ACCATTATTAGTTAG[C/T]TACCTTTTTATGGCA | 57626 |
rs184740618 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798018 | AGCAGCTAAATTACT[C/G]GTGAGATTTGTTTTA | 57626 |
rs184753479 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893856 | AGGTATTTGTTGTGC[A/G]TGAAAGAGCACCCTT | 57626 |
rs184756910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850535 | ATGAAACTGTCTACG[A/G]CCCTTCCATTTCATT | 57626 |
rs184761890 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871185 | TTACCACTTGTGCCC[C/T]CCGGAACAATGGCCT | 57626 |
rs184769944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802107 | CACTTATGAGTGAGA[A/G]CATGCAGTGTTTGAT | 57626 |
rs184779231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933803 | AGAGAAGGGGGAAAA[A/G]AAAATACTTGAGAAA | 57626 |
rs184789407 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721074 | TAAGATATATATATA[C/T]ATATAAAGCTATGTA | 57626 |
rs184801517 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856881 | CAATTTCATAGTAAT[A/C]CTTTTCCCTCCCCAA | 57626 |
rs184805348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838473 | TTAGTTTTTAAACAA[A/G]TAATTTATTTTCTTT | 57626 |
rs184808222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823432 | TTAGGCTCTAAAGTC[G/T]ATATATAAGCCAAAA | 57626 |
rs184812832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894276 | GTATCATTGGCCAGC[A/G]TAATCCTGCTTGTGC | 57626 |
rs184818192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992000 | AGCTGTGAACTTGCT[A/G]GGAATGCAAAGTACT | 57626 |
rs184818677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915437 | CCTCAGAAATAATGC[C/T]GCATATCTACAACTA | 57626 |
rs184821789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958806 | CTCATTCATTTTTTT[C/T]CCTGTTTTCTGGAAT | 57626 |
rs184824788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031221 | AGGTTTAAGAAGCAT[C/T]GCAAGGATCATTCAG | 57626 |
rs184825509 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922163 | TGTTACCCAGGCTGG[G/T]CTCTAACTCCTGGTC | 57626 |
rs184829052 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942631 | AACCCACCCATATAA[C/T]CTTCATCTGGCTTCA | 57626 |
rs184835384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762414 | GGCTTTAAAGCATTA[C/T]GCCAAAGTGTATTTT | 57626 |
rs184836521 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974940 | CTGACAGATTGAACT[C/G]TAAATCACCTGCAGT | 57626 |
rs184847180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068592 | TATACAGTGGGTATG[C/T]ACATGCTACAGTGTG | 57626 |
rs184850973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008782 | TATGCCAAAACAAAG[A/T]TAGCAATTTAATTAT | 57626 |
rs184852059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991330 | TGAAGAATATAGAGA[A/C]ACACAAAAAAAGCAC | 57626 |
rs184854903 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861700 | CACGCCTGTAATCCC[A/C]GCACTTTGGGAGTGT | 57626 |
rs184867393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798135 | CTGATCTTGATGTAG[C/T]GTTTGACTTCATGTT | 57626 |
rs184868512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030232 | TTGAACTCAGCTCTG[C/T]ACCAAGCGGACCTAA | 57626 |
rs184925610 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69716215 | TTGTCTGTATAACAA[A/C]CTATTTACAGTTTAT | 57626 |
rs184931372 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735239 | ACTGCCTTTAACCTT[A/G]ATCAATATATGTATC | 57626 |
rs184937149 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783044 | CTGTTTTCCAGCCAC[C/T]GCTGCTGATACCCAG | 57626 |
rs184946008 | snp | C/T | 0.000727868 | 0.0190632 | utr-variant-5-prime, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107704 | GAGCCTGACATGCTT[C/T]ACGCACAGAAGGCAA | 57626 |
rs184946371 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077297 | AAGATATGAGCTCTT[A/G]AGTCTCAAAAATACA | 57626 |
rs184954286 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973091 | ATTATTTTTCATGCA[C/G]AAATATATTAATGGG | 57626 |
rs184958315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995179 | AATTATGACAGAGAC[A/C]ATATACCCCACACTC | 57626 |
rs184963915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741540 | ATCAGAGTACCATCA[A/G]TTTTTGTTTCTGTTG | 57626 |
rs184966049 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817420 | TACATGTTTTCCTTT[A/T]TCATAAATGAGCACC | 57626 |
rs184973173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035347 | AGAAAAACAAACTTC[A/G]TATGTTCTCAATTGT | 57626 |
rs184982446 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840906 | CTGTGTGTCAAATAT[A/G]TAGTTTCTTGTATCT | 57626 |
rs184983443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721785 | GTGTTCCCTTGATGC[A/G]TGTAATACCTCTTTG | 57626 |
rs184986422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070610 | CATAAGAATGTTAAA[G/T]AAGTTATTCAGAATA | 57626 |
rs184989122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754832 | TATTTTGCTATTACC[C/T]GAATGTTCCCTGAAT | 57626 |
rs184992312 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742158 | AGAAGGGTTAATTGA[A/T]ACCTGTACATGCAGT | 57626 |
rs185012440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763210 | ACAGAATTGACCTAG[A/G]TTACTTACTGGCTGA | 57626 |
rs185022412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704040 | CAACTTTCCCAAAGG[A/C]TCCCTGATGTCCATT | 57626 |
rs185046826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798696 | AGCAAACTACATAGT[C/T]GAATAACTTCAAAGT | 57626 |
rs185048077 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978728 | CCGAACTCAGGTGAT[A/C/T]TGCCCGCCTTGGCCC | 57626 |
rs185054067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783150 | CTAACAAACAGAAAG[C/G]ACATCCACAACAAAA | 57626 |
rs185063257 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090485 | TTTATTGAAAAAAAA[A/G]ACAGAGAAGTTAAGA | 57626 |
rs185066054 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015517 | TCAATTTTTTGACAG[C/T]GCAAAAGCAATGCAT | 57626 |
rs185079269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094967 | TGGCTATCTTCTATA[C/T]CCAGTCCCCATTGCT | 57626 |
rs185088956 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054025 | TCCTCTCATTTCTGG[A/G]AAAAATGTGAGTATT | 57626 |
rs185104152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746312 | CTATTTTGGCTTACT[A/T]CAATGACATTATATG | 57626 |
rs185104443 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822546 | GAAGTCATTACTTAT[A/T]TCTACCCACGCATCA | 57626 |
rs185108315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716495 | CTTTCTGGTCAAATT[G/T]GCAATATGAAATGAT | 57626 |
rs185124893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993051 | ATCATTTTTAGTGTC[A/C]ACTAACACTATTTAT | 57626 |
rs185131173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011820 | TTGGGGGTTCCGTAT[A/T]TGTCCATTTTCATGC | 57626 |
rs185133574 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032218 | GAAGTGGAGCAAGGA[C/T]GTAAAAAGACTTGAT | 57626 |
rs185147397 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885232 | GGCGTGAGCCACCGC[A/G]CCCGGCCCTTCTTTT | 57626 |
rs185148120 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051358 | GGTTACATCTATTAT[G/T]GATAATTGCCTTCAG | 57626 |
rs185155071 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724115 | GCTGGGATTACAGTC[A/G]TGAGATACCGTGCCT | 57626 |
rs185162496 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966448 | TGAGACTTACTACTC[A/G]TTGACAATGTTCCTG | 57626 |
rs185165834 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69998024 | ATGTTGTGAAGAACT[G/T]CAATACTGTTTTCTA | 57626 |
rs185168668 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69981724 | ATATTTTATATCAGG[C/T]ACACATTATTTTAAA | 57626 |
rs185171396 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69922204 | CTCCTGCCTTGGCCT[A/G]CCAATGTGCTCGGAT | 57626 |
rs185174486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019297 | GTGAGCCTGGGGAGA[C/T]GGACTAATAGGAAGA | 57626 |
rs185189262 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037888 | TATTTCTTCATTATA[C/T]GTATAATTCCCTTTT | 57626 |
rs185191747 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767121 | TTAACTTAATTATTG[C/T]TATATTTATTAACTG | 57626 |
rs185193460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056791 | TGAAAATGGAAACAC[A/C]ATGTACAAAAACTAT | 57626 |
rs185201005 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086883 | GTGTCAGCAGGTGTC[G/T]AATAGGATACAGCTA | 57626 |
rs185202755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959267 | ACAGGAAATGCAAGA[C/T]TGCCAGACCATGGAG | 57626 |
rs185203162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072686 | ATCAACAAACTGAAG[A/G]AAAAAAAAGGGGGAT | 57626 |
rs185210440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991648 | TAATGAGCTCTGAAA[G/T]GGAATCAGTAATAAA | 57626 |
rs185223133 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801502 | TTGCATTAGCTTTAG[C/T]AGGCAATTATGTTGT | 57626 |
rs185244949 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021717 | GTGCCTCAAGTGAAG[A/C]CCCAAAGACTCTTCA | 57626 |
rs185254171 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837547 | TACAATCATAAATAG[A/G]TATATTTGTATATAA | 57626 |
rs185263239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060206 | GAGATCATAAGAGAA[A/G]TAATGAGACATCATC | 57626 |
rs185289415 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69827361 | ACTGATTCTAATCTT[C/T]AGTAAAATTCTAAAT | 57626 |
rs185314202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975127 | CTTTAAAAATAATAT[A/C]AGTATGACACAATTT | 57626 |
rs185318095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741393 | TGATTATAAAGAAGT[C/G]TGAAGCATCTGTGAG | 57626 |
rs185319512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881668 | GAACTTCATGTTCTT[A/C]TTAATTTTTCTGTAC | 57626 |
rs185327617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843222 | ACACACTATATGCAC[A/G]TAACAAAATTTCTCA | 57626 |
rs185333217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863838 | CTGTCAGTAATAATT[C/T]TTTCTCACTAATATT | 57626 |
rs185337421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920541 | TGAATTAATTAAGAA[A/G]ACTATATTGAGGAGC | 57626 |
rs185352602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939897 | AATACATTATGGTAC[A/G]CTATAGTTCATAACA | 57626 |
rs185355128 | snp | G/T | 0.00676609 | 0.0577691 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701390 | ACAAATATTGGTCTC[G/T]CCTTTCAACTGCTCA | 57626 |
rs185356666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899396 | GTTCACTCATCTAAA[A/G]TTGTGTGGCAAGGTC | 57626 |
rs185368038 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040950 | TCTCTCTGTTTGTTT[C/T]ACAGATTGGGTGACT | 57626 |
rs185382594 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773659 | TTAGTCAAGGTCTTT[C/T]GAGTATGGAGCACAG | 57626 |
rs185388590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074907 | TTCCTATAATAATTT[A/T]AGTAAAAAATCAATA | 57626 |
rs185390528 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841915 | CTGATCTTTAAGAAA[G/T]TCAACAAGAACTTAC | 57626 |
rs185409773 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807223 | TGCACTCCCCATGGC[C/T]TCTTGTTGACACTGC | 57626 |
rs185416213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984935 | CCAACATGGAGAAAC[A/C]TGGTCTCTACTAAAA | 57626 |
rs185423669 | snp | A/T | 0.00637571 | 0.0560999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909544 | GGGATAATTTTTTTT[A/T]AAAAAAATCAAAAGT | 57626 |
rs185423902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945680 | ATATTATCAGTGCTT[A/C]AGAAAATGCACATTA | 57626 |
rs185427717 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880927 | AACTGATAACTATCA[C/T]TGGCTTTCTGGCTAA | 57626 |
rs185433075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022157 | ATCAATTTTGGGGGA[C/G]GGTATAAGGTTTGTT | 57626 |
rs185435081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041539 | AGTTCAGGCTCCCTA[C/T]TTTTGTTTCTACTAG | 57626 |
rs185449066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060708 | AAAATTAGCTGGGCA[C/T]GGTGGTATGCGCCTG | 57626 |
rs185450896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978020 | TTTAAATATTTGAAA[C/T]TAATACAAATTTTGC | 57626 |
rs185455414 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076703 | CAGCAGAATGTAAAG[A/C]CACAGACCAGGAGAA | 57626 |
rs185456737 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091545 | GCAAAATTTTCAATT[A/G]TGAAGTTTGTGGATC | 57626 |
rs185479621 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720392 | CCATTTGCTCACTAC[A/C]TATTTTTGAATGGTT | 57626 |
rs185496568 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043912 | TCTAATCTGACTCAT[C/G]ATCTCTCAATCACAC | 57626 |
rs185497451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790000 | TTGTCCTCACCAGGC[A/G]TTCACCGAGATGTAA | 57626 |
rs185509928 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748421 | GGAAAATGCAAAAGC[A/G]GAATCCCCTGATAAA | 57626 |
rs185512924 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70079987 | GTGATGGTGAATCCC[A/G]TAGTTCTTGATCCAA | 57626 |
rs185521118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888699 | TGACTTTGAATTTCC[A/G]GTCATTAGAACTGCA | 57626 |
rs185529669 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69826552 | GCCGTTGCACTCCAG[C/T]CTAGGCAACAAGAGC | 57626 |
rs185533222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831231 | AAGAAGAGAGAAGAT[C/G]AAAATAGGCTCAATT | 57626 |
rs185534993 | snp | A/G | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787704 | ACAGCAAAAGAAACT[A/G]CCATCAGAGTGAAAA | 57626 |
rs185538888 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708810 | AGAACCCAGAAGAAT[A/G]AATATAAAATAAAAC | 57626 |
rs185545186 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770119 | GAGAGAGCTATAACA[C/G]CCCCTTGGGACTCCA | 57626 |
rs185547488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726892 | GATATATCATCATGA[C/G]CAGTACATGTTTGTG | 57626 |
rs185555986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862892 | CAGAACTGTGACAAA[A/G]TACATTTCTGATGTT | 57626 |
rs185561644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868344 | TTAAAATATAAACAT[A/G]GTAAAATCATTAATG | 57626 |
rs185562178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926670 | CCAAGAATTCAGGCC[A/G]GGCGCGGTAGCTCAA | 57626 |
rs185566898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838896 | TTTATGTCATTTTTT[A/G]TAGTATCACCATTAC | 57626 |
rs185566973 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104928 | TACTGCATATTAAAA[C/T]ATTATATACTGATAA | 57626 |
rs185568611 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885592 | TAAAAGAGAAAATAT[C/T]AATTCCCATTGAGTT | 57626 |
rs185568990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846617 | TTTGGTTAGAAAAAA[A/T]TATATATATGAATAA | 57626 |
rs185571360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964196 | TCACAAGTATATGCT[A/G]CCATGCCTAGCTAGT | 57626 |
rs185573563 | snp | C/G | | | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108136 | TGTGGCAGAGCCTTA[C/G]TAGGGAAGGTGGTGG | 57626 |
rs185574804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824196 | TTCTGGTATAGCAAA[G/T]AATGTTTCTATGTAT | 57626 |
rs185578292 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70087913 | CACACACTGGGGCCT[C/G]TTGGGGTTGGGGGCA | 57626 |
rs185580678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803027 | ATTCCCACTGCTTCT[C/T]TCGACCAGCCTTAAA | 57626 |
rs185601340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906125 | TTATTTCCTTCTCAA[C/T]ACCGCATGAGAACTA | 57626 |
rs185608971 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69793660 | TATAAAACCTCTGCA[A/T]ACCACACATAGATAC | 57626 |
rs185621265 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69891312 | ACAAAATATGAGAGT[A/G]TTAATTTTTTAAAAA | 57626 |
rs185631598 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912810 | TCCCTTGGCTGGTTC[C/G]TGAAGAGGCCCCATG | 57626 |
rs185633861 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873187 | AAATAGTGAACTAAT[A/G]TTAGTCAAAAGTAGG | 57626 |
rs185634690 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70063272 | TTTTTTTCTAAGAGT[G/T]ATTTTATTTCAGGGA | 57626 |
rs185645470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828883 | CACACCTCCATCCCC[C/G]ACAGTGGCCACAGCA | 57626 |
rs185649944 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929315 | TTATCTCATTTTATA[C/T]TCAAAGTAGGTATTG | 57626 |
rs185660728 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965909 | GCTGAGAGAGGTGAC[A/G]AAACTGCAGAAGAAA | 57626 |
rs185663726 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902743 | GGGAACATCACATAT[C/T]GGGGTCTGTTGTAGG | 57626 |
rs185664745 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948464 | AACTGCTTATAAAAT[G/T]GGAGTCACCCTCCTC | 57626 |
rs185665830 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866832 | TTAGAGGTAATAAGA[A/C/G]GGCTTCGTAATTCAG | 57626 |
rs185671184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981241 | AAATTACACTAAATA[C/T]AGTAAATAAAATACA | 57626 |
rs185692523 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997787 | TAATATAATATATAA[C/T]ATGTATTTTATATCT | 57626 |
rs185744966 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001714 | TCTTTCTACTATCTT[C/T]CTATCTTAAATAGAT | 57626 |
rs185750129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778099 | ACTAAAGAAGATAGT[A/G]AAACAGTTAATTAAA | 57626 |
rs185754747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751578 | GAACTGAAAGAAGGC[C/T]GATGTGGCAAGAAAA | 57626 |
rs185757773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970501 | CCAGGGGCAGTGATG[C/T]TAGTACCTAAAGCAC | 57626 |
rs185760847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722837 | ATATTCAAAGGAAAT[G/T]AAACCAGTATATAAG | 57626 |
rs185772571 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845621 | ATATACCTGACAAAA[C/T]TTCAAGTACATTTTA | 57626 |
rs185776019 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790487 | AAACCAGACAGAGAC[A/T]TGATAACTAACTCTA | 57626 |
rs185781293 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70003193 | ATCTTTTCTCCATAA[G/T]ATTGCACATATTTTA | 57626 |
rs185785082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810769 | GAAGATCCAATCAAA[C/T]ACAGTCAGAAATGAC | 57626 |
rs185785977 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774297 | TATGACATAAAAGTA[A/C]AAATATATAGTTGCA | 57626 |
rs185792262 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731180 | TGAGTAAAGTGACAA[C/T]ATTAACACAAATGAA | 57626 |
rs185793169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068866 | TCGTCGTGGGGGAGG[A/G]GGCACACTTTCCTGA | 57626 |
rs185803379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041824 | CTTGTTATTGCCACA[C/T]TGGGATAGAATACCA | 57626 |
rs185806386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842376 | CCATTAAAAAGTGGG[C/T]GAAGGACATGACTAG | 57626 |
rs185812662 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102347 | GCATATTGTTTATTA[A/G]TTATAAAATAAAATA | 57626 |
rs185820115 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808701 | TTTCAGTAGCTTCCA[A/T]GCAATGGATCCTAAC | 57626 |
rs185820403 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084773 | AGCCACTGCGCCGGG[C/G]CGTCTATTTCATATT | 57626 |
rs185853447 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796465 | ACCTGCTCCTGTCTC[C/T]CTTGCTTCCTGTGTA | 57626 |
rs185858936 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949973 | CTTCTAAAAATTACC[A/G]CAAAATGATTTTAGA | 57626 |
rs185868296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714245 | TCTATTTTGACTTAC[A/G]TCATATTTTATTACA | 57626 |
rs185870592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848415 | AGGAGTAGATAGTTC[C/T]TCCTCTTACATTTAA | 57626 |
rs185870610 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895118 | TCTTCTAATGGTTTC[A/C]TTTGTTCCTTATATA | 57626 |
rs185872042 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983998 | CTCTCACTACTTAAA[A/G]TCAACTAAAAATAGG | 57626 |
rs185874697 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096840 | AGGGAAAGCATAGAG[A/G]GAATCTTCTCAGCAA | 57626 |
rs185879593 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832340 | ATCAAGAAATCAACT[C/G]TTTTTAAAATAGCTG | 57626 |
rs185883817 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021550 | TGATTGCTGAATCTC[A/G]TGGCAAACGTATATC | 57626 |
rs185893365 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69934916 | GAGGGTTCCCATTGC[A/G]TCTCATAATTTTTCT | 57626 |
rs185893598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952293 | TCCAAGTAGTATTTA[C/T]GTTTTTCAGGCATGG | 57626 |
rs185901338 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985395 | AAATGAAAAATGCTC[A/G]ACTTCATTAATCATC | 57626 |
rs185904891 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818938 | GTCATACAGTATTTT[A/C]ATGTTATTTCTCCAA | 57626 |
rs185911255 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69887519 | CTATAAGCAGTTGAC[A/G]AAAGCAACGTGGCTC | 57626 |
rs185911315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951425 | GCAAGTTAGTAGGAA[C/G]ATGTTTCTGTAGAAC | 57626 |
rs185921441 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984200 | ATTTAGGCAGATAGT[A/G]AGGGTACGGATGTCC | 57626 |
rs185923358 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69968494 | GAAAGGGAGAAGACT[G/T]AAAAAAAAATCAAAC | 57626 |
rs185926562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023190 | AAACATATCAGCTCT[A/C]TCAAATCTATCAAAA | 57626 |
rs185938478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061161 | CTCACTTAATGTTTT[A/C]ATCAAATTTTCTGTT | 57626 |
rs185938957 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69752319 | CCTCTATTTCTGAGG[A/G]CTCTATCTATGTTTG | 57626 |
rs185954168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791264 | TTTAGGAATAAATTT[A/G]GCAAAATAGGTACAA | 57626 |
rs185958368 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083512 | ATTAATTTTAGACTA[A/G]TGATATACTTATTAA | 57626 |
rs185997990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708175 | TTAAAAATCTGGGAG[C/G]ATTGTGGAATACTCG | 57626 |
rs186010957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726103 | TTTCATACTTTACCA[A/G]TAAAGGATATTTCAA | 57626 |
rs186021368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989130 | CTGTCTTGAAATGAT[A/T]TTTGTATATAGTGTA | 57626 |
rs186042131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775769 | CATCTTAGCTCACCA[C/T]AATCTCTGCCTCCCG | 57626 |
rs186047853 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028356 | TTCAGTATATATATA[G/T]ACAGAGGTATGTCTT | 57626 |
rs186061708 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732466 | GGAGGAAGTACAAAC[G/T]TTTTAAGCTGTTGTC | 57626 |
rs186062647 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065371 | ATTCTTAGTCAAATC[A/T]CTCTAGATCATGGCA | 57626 |
rs186076811 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809582 | ATGGAAATGAAAGGA[A/T]TATACTTGCTATCAC | 57626 |
rs186078799 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101510 | CTCGGCTTACTGTAA[A/C]ATCCGCCTCCAGGGT | 57626 |
rs186082777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834244 | ACCTATTGAAATTAA[A/G]TAAATAAGTACATAA | 57626 |
rs186092988 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799390 | ATTCAAAAAGGAAAA[G/T]TCAGGAATTGATTTG | 57626 |
rs186101155 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783352 | TGAGTTGAGAGAAGA[A/C]GTCTCCAGACGATCA | 57626 |
rs186109663 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853153 | TAAACTACTGATATG[G/T]TTTGACTGTGACCCT | 57626 |
rs186117812 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092735 | AAGAGAAATTGCTCA[C/T]GTTTTACAGTATAGG | 57626 |
rs186125666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834486 | TTCAAAATATTACAA[A/C]GGTGAATTTCACATT | 57626 |
rs186131706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819722 | CTACTGTGGCCCTAA[C/G]ATGCCATCAGCATGC | 57626 |
rs186133532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101400 | CTGGAGTTTTGGGTA[C/T]CTGAAAATCCAATTC | 57626 |
rs186150558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872787 | GAGGGGCAAGGCTCT[C/T]TTTAACAACCGGCTC | 57626 |
rs186153754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948814 | TTATATTGAAAATGT[A/G]TATTTCCAAAGGTAT | 57626 |
rs186153983 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973535 | CACCACATACATTTT[C/G]CTTAAAGACAATATT | 57626 |
rs186156306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779165 | TTAAAAAATCTTCAA[C/T]AAATGTTTATTTGAA | 57626 |
rs186158795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890652 | CACACACACGCACAC[A/G]CACACACACACACAG | 57626 |
rs186172276 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006541 | TTGAGAAGGATTTGT[A/G]TTAGTTATTTGTTAA | 57626 |
rs186182875 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045042 | TGTATAATATTCATA[C/T]AGGAAGTCATTTTGA | 57626 |
rs186183288 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69736231 | AATTGGGCTAAGGAC[A/G]TGAATAGACAATTCT | 57626 |
rs186186093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811850 | GATGTTTTCAAAAAA[A/C]CAGCTCCTGGATTCA | 57626 |
rs186195332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033259 | GTAGGGACTGCTGTT[A/C]GGCTTCTAATAATTT | 57626 |
rs186199570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051604 | TGTCCAACACTGATA[C/T]TGTCTAAAGGAGGTA | 57626 |
rs186210366 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069214 | GTGGTCCTGTATAAT[A/T]AAAAGGAGATTACAG | 57626 |
rs186250166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713436 | TCTCATTATCAAATT[A/C]ACAACATTAATTTAT | 57626 |
rs186255203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717251 | TTCTAATGATGTTTG[A/C]CTATGATTATATACT | 57626 |
rs186257511 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730037 | TAGTCAATTTAAAAG[A/C/T]GACAGTAGAAGAAAC | 57626 |
rs186266336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952131 | AATCTGGCAAATAAA[A/G]TAGTAATTTGTAAAA | 57626 |
rs186271113 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915925 | AACCGCATCAAAAAG[C/T]GGGCAAAGGATATGA | 57626 |
rs186322005 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013274 | CTTTCAAAAACACTT[C/T]CAACAAAAAAGAGAA | 57626 |
rs186323250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737131 | AGGCAGTGAGGGATT[A/G]TGCTACCCCTCCTTG | 57626 |
rs186334828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757661 | TACTTAATCAAATAA[G/T]ATCACATGTTGGCCT | 57626 |
rs186339832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756817 | ACCATGAAAATAATT[C/G]AAAGATAATCCACAT | 57626 |
rs186342252 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052094 | CCGTGCAATAGGCCA[C/T]TGAAGTTCAATCCAG | 57626 |
rs186348393 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795012 | TCTTAGGCCGAGGAT[A/G]TTTATTGTATTTGAG | 57626 |
rs186358119 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785984 | TCTCTGAATAGACCA[A/G]TAACAGGCTCTGAAA | 57626 |
rs186363214 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920878 | AGTAAAGATTGCACA[C/T]GAAATAAACAGGGAT | 57626 |
rs186366461 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717803 | ATTTGTGAGTATAAA[A/T]GCATAAACCTATTTA | 57626 |
rs186380552 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955343 | AACATTTCTTAGCAG[G/T]TACAAAGACTTTAAT | 57626 |
rs186388702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940411 | AGAATTTTGCATTTC[A/G]TATTTCATGTAATAT | 57626 |
rs186390896 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974119 | ATAGTAATGTACTTA[A/G]GTTTATCACTTAACA | 57626 |
rs186394450 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69779858 | TGCTGTTGCCCAGGC[G/T]GGAGTGCAATGGTGC | 57626 |
rs186397426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097699 | CAGTCTATATGTATT[C/T]TACTATCACAATTGC | 57626 |
rs186403217 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895280 | CCACTCTAGTTGGTA[C/G]AAGAGGTTCACACTT | 57626 |
rs186403473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858852 | AGAAAGAAAGAATAC[A/G]TCCAGAGGAATGAAA | 57626 |
rs186404154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007212 | TGTGTCGTATTGCAA[C/T]AAATCAAATGTGTAT | 57626 |
rs186404434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989706 | TATTTCTAGGTATTT[A/T]ATTTTATTTTTTGGC | 57626 |
rs186412601 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055194 | AGGGAGGAAACATAA[A/C]AAGGAGCTGCAATAC | 57626 |
rs186418473 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071839 | AATACAGTACATACA[A/G]CAAAATTGGAAGTAT | 57626 |
rs186420132 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029079 | CTATATAATGACTGT[A/T]TATTGCAATTATTTT | 57626 |
rs186424558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045697 | ATATGGAGTTTTAAA[G/T]AAATATTTTTTTCCT | 57626 |
rs186431925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935598 | AAGATCTGAATGAGG[C/T]AGAGAAGAAACAGAT | 57626 |
rs186435671 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969537 | AAAAAATATATCAAC[A/T]TAAAGTTAACCAGCT | 57626 |
rs186474646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799787 | ATCTTCTAGAACAAG[A/G]GTCCCCAACTTCCAG | 57626 |
rs186482525 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69977970 | TATATTTATCTACAC[A/G]ATATGTTATCTTCAT | 57626 |
rs186485206 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69765628 | TCCTATCCTAATAGA[A/G]CCACTAGTTTTTAGC | 57626 |
rs186489975 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109548 | AGTTGGACGCTTTAA[C/T]AAAATAAGAAATTAA | 57626 |
rs186492591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834755 | AGAGAATGTATAACA[A/G]AAGAACAAATGAGTA | 57626 |
rs186493782 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963702 | TTGCAACATAAAACA[A/C]CCCTTCTGCTCAGTC | 57626 |
rs186494251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898870 | TGTGAACGAGGCCTG[A/G]AGACTCACCATTGAT | 57626 |
rs186496217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994438 | AGGATTTTACCAGGA[C/G]CAGATACTTTGCAAT | 57626 |
rs186501865 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863509 | TAAGAAATAAAAAAA[A/T]TTTGCATTTTTCATG | 57626 |
rs186516940 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939496 | ATATGCTGTGACGGA[A/G]AGGTTTAAAAAATGC | 57626 |
rs186520391 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014138 | ATCTATGCTTCTCAG[G/T]TACTTATGTGGAGTA | 57626 |
rs186534339 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033896 | GATTACAGGCGTTAG[A/C/G]CACTGCACCTGGCCT | 57626 |
rs186536537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034096 | AAGAATCACCTCAAG[C/T]GCAGCACTGAAATGC | 57626 |
rs186547738 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052607 | TTTTGAATAGCTAAT[G/T]TTATGTGCCCATATT | 57626 |
rs186552518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069890 | AGAAGCAGATGAGGC[C/T]GGGCACGGTGGCTCA | 57626 |
rs186556246 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070449 | AAAAAGAGAGTGGAG[C/T]AAAATATTCAAAATG | 57626 |
rs186574348 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037586 | TTACCTTGGTATCTT[C/T]TTGTCTCTTCTTTAG | 57626 |
rs186585666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943841 | AGTTGTCAAGAAGAC[A/G]GTTGCATGCTTCTTA | 57626 |
rs186589303 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895944 | AACTTGTGACCTCAG[G/T]TGATCCACTCACCTC | 57626 |
rs186592359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936689 | AATAAAACACTCAAT[A/G]TTCTAAGTTTAAAAG | 57626 |
rs186592844 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072325 | ATGGAAGGTACAGAA[C/T]GCCCAGATGTTTTTA | 57626 |
rs186595605 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960307 | GTAAAAAATAAAACT[C/T]CTTAAACTACGTTCC | 57626 |
rs186596846 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916864 | ACAGAATATTAAAAA[A/G]CAAAGAATCTTATCA | 57626 |
rs186625067 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69744488 | TGTTTCAAAGTATAA[C/T]ATATATATATTACAT | 57626 |
rs186627680 | snp | A/C | | | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110293 | TCTATATTTGTCAAT[A/C]TTAATACAATATATA | 57626 |
rs186635018 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092898 | ACAGTATTGAACAGC[A/G]CAGCCATGAAATAAT | 57626 |
rs186649667 | snp | A/G | 0.123798 | 0.215808 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713717 | GAATATTTTTTTTTC[A/G]TATTTTAGTTTATAA | 57626 |
rs186675683 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69784183 | AGAGCTCCTGAAGGA[A/C]GCACTAAACATGGAA | 57626 |
rs186675945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748039 | ACTAGAAAGTTTACC[A/G]TCTCTCTACTGGAGA | 57626 |
rs186679535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845616 | TTTCTATATACCTGA[C/T]AAAATTTCAAGTACA | 57626 |
rs186702653 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69881485 | ATACAAACAAGTTTA[C/T]CCATCAACTTAGAAG | 57626 |
rs186703523 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902482 | AGGGTAAATAGTGAA[G/T]AATTAAAATAATTTT | 57626 |
rs186704183 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853893 | GAGACTTTGCTTAGC[A/G]TAAGGCTTAATAATA | 57626 |
rs186708065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092412 | TATGTGTTTCCAAAG[A/C]CTTACTCTCTCTTTA | 57626 |
rs186712711 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866462 | CCATTAAGAATCCCA[A/T]AGTTAAAACAAAAAT | 57626 |
rs186713498 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786022 | AATAATCAACAGCTT[A/G]CCCCCCAAAAAGAGT | 57626 |
rs186714291 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820685 | CACTACAGGGATGCC[G/T]GTTCAAGGGACATTC | 57626 |
rs186718819 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884238 | TGTATAATAATAATA[C/T]AATTTGTAAATAATG | 57626 |
rs186719230 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942046 | GAGTTGGTGCCAATC[C/T]TACTGAAACTATTCT | 57626 |
rs186732524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921894 | AAGGGAGTACTTAGG[A/G]AGTTATAGATTTTTG | 57626 |
rs186733971 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957847 | TTGAAATTGCTTATA[A/C]TGCTAATTAAGAATT | 57626 |
rs186734474 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919983 | CTCACTTGCTTGCTT[A/G]TATCATGATGTAAAT | 57626 |
rs186738703 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857836 | ACGTACCCTAGAACT[G/T]AAAGTATAATATAAA | 57626 |
rs186745640 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823820 | TCATTGAAATTTTTT[C/T]TCTCTCTCTCTCTTA | 57626 |
rs186747885 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70088136 | AAGTAAATAATGAGC[A/G]CCACGAACTTTCAGT | 57626 |
rs186749340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954647 | TATTTCTTTTGCAGT[C/T]TCTCTATTAAGCCCC | 57626 |
rs186750447 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974794 | TAATTTGTGGTTTTG[A/C]CACACATATTATGAC | 57626 |
rs186781727 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785119 | GGATGGTCTCGATCT[A/C]CTGACCTCGTGATCC | 57626 |
rs186781821 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704934 | TATCTATTGTCTACA[A/C]ATAAATGAAATGCAT | 57626 |
rs186787481 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766168 | TCCTATATATGAATA[G/T]TATTGACCATGAAAT | 57626 |
rs186789089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723288 | ACGACTAACAATAAT[A/G]CATTGCATAGTTTGA | 57626 |
rs186794032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745390 | GTCAATTTTAAAAAG[G/T]ATACTTATTAATTCT | 57626 |
rs186797220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018138 | GAGTGAATAACTTAC[A/G]GGAAGCTAAATAACA | 57626 |
rs186809411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821248 | ATCATAAATTATTAC[A/G]AGAAAATAAAGATTT | 57626 |
rs186811721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800802 | AGGACAAAGTCAGTC[A/G]TGAGTAATTTTAGCC | 57626 |
rs186814559 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69923640 | TTATAAGAATAAAAT[A/T]GTTGATGAAAAATTA | 57626 |
rs186816785 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70055475 | AAGAAATCCTCAGAA[A/G]ATACAAAAGTCAATG | 57626 |
rs186837118 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961136 | ATATGTATACATATA[C/T]ACATTTGTAATTTCA | 57626 |
rs186845875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993708 | TCTGGATGCCTTATT[A/G]TTTAATTTGTTCCCC | 57626 |
rs186846255 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107094 | GGTGGCATCTCTTAA[A/C/T]CCACATTTTCAACCT | 57626 |
rs186853097 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089998 | ATATTTTTACTGGCT[G/T]AATCTCCTCTGAAAA | 57626 |
rs186899824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805806 | TACTTATTTCATAAT[C/T]TATTATATAACATTT | 57626 |
rs186905703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749940 | TTATGCAAAATAATA[A/G]CAATGAAAAGCTAAT | 57626 |
rs186907467 | snp | A/G | 0.00370065 | 0.0428559 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789327 | TAAGTCTTATTTAAT[A/G]AATTAAAAATATAAA | 57626 |
rs186913749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772895 | CAAAGCACTAGAGTG[A/T]TTGATTCAAGAGATA | 57626 |
rs186915486 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69887858 | TCAGTTTATTCTAGT[A/T]TGCATTTCAAAATTC | 57626 |
rs186920986 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908503 | TTATATAGTTTATTT[A/G]CTGCCTAAATCTAGT | 57626 |
rs186922547 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69861745 | CTGAGGTCGGGAGTT[C/T]GAGATCAGCCTGACC | 57626 |
rs186922857 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802685 | GCAGCCCCCCAGTCC[A/C/T]GTACCCCCTGCTTGC | 57626 |
rs186926963 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870846 | ACTAGTGTGAGAGGT[A/G]AGAGGTGGGCTCTCA | 57626 |
rs186932752 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841022 | TCATTTTTCTTCTCT[C/T]CTTTTCACTCCTTTT | 57626 |
rs186934985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825075 | GTTGCATACTAGTAA[C/T]GATATCACTTAGATG | 57626 |
rs186937173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768832 | AATAATGCTTGAAAT[G/T]TAGGTGCTTACAGAA | 57626 |
rs186938384 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039679 | GAGTTTTACTTTGTC[A/G]CCCAGGCTAGAGAAT | 57626 |
rs186944841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924692 | CAGAGCTGAAACACG[C/T]CCCTTGCTCATCACG | 57626 |
rs186948690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962151 | TTTGTTTCCTTTTCA[A/G]TTTTAAAGTTTTCCT | 57626 |
rs186949273 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704208 | AAAAAACAAAATGTG[A/C]TATTCCCCTTGTGTT | 57626 |
rs186949956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059076 | AAAAATGGATCAAAT[A/G]CTAAAACCTCAAACA | 57626 |
rs186952637 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105617 | ATATAAGGTGAATTG[C/T]TTAATGTTTCTGGAT | 57626 |
rs186952797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838746 | CAAATCTCTTTTTTA[C/T]TTTATATGAACTCTT | 57626 |
rs186955672 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074327 | TCTGTCTGGTCCCTC[C/T]ATAATCTCGGATCTA | 57626 |
rs186960141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944752 | CACGGACCTATATAA[C/T]CCAAACAATTCTGAA | 57626 |
rs186963371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977055 | TGATTTCATTAAGCT[G/T]AACTTTTAATTGAAG | 57626 |
rs186985788 | snp | A/G/T | 0.00835141 | 0.0640778 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700392 | GTTTTCTGGGCACCA[A/G/T]TGATAACTGTCTCAA | 57626 |
rs186997904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908306 | TAATTTCAAAGGGCC[A/G]AGAAGATGGGAAGAT | 57626 |
rs187016851 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743956 | TCTATTTTGGATATA[A/C/T]CATGTTTAAAGGGAC | 57626 |
rs187022805 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944644 | TTTCATTTCACACCA[A/G/T]ATTAATCTATAGATG | 57626 |
rs187049854 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976827 | CTCTACTGAGGCAAT[C/G]AGGACTTAGAAAGCT | 57626 |
rs187067102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911705 | CACATCAACTGTGGA[A/G]ATACCTGGTTTGTGA | 57626 |
rs187088883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843735 | AATTTCAATAAGTGG[C/T]ATCTTCTACTGAGGT | 57626 |
rs187098173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948132 | AATCTCTCTTAGCAA[C/G]TCCAGAGGAACTTTG | 57626 |
rs187111085 | snp | G/T | 0.00480355 | 0.048772 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882527 | TCTTGGCATAAATTC[G/T]GTTTCACTTTTATTT | 57626 |
rs187130342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980866 | GAGTTCAACAACTAT[G/T]TGTTGAATAAATGCA | 57626 |
rs187139702 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809901 | AGCAGGATCACTATT[A/C]GTTTATCAGATAAAA | 57626 |
rs187142610 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017970 | AACGTGAAAATAAGC[A/G]CTAATCTCCAATTAA | 57626 |
rs187149656 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69791572 | GAAAATGTGGGAATG[A/G]CATAAAGATATACAC | 57626 |
rs187152969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753230 | ACCCAAACCTTCATA[A/G]CTGTTAAAATAAAAA | 57626 |
rs187155843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777171 | ATCATGTAAGACGTG[C/G]CTTTGCTCCTCCTTC | 57626 |
rs187161863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844514 | CATTTCGTCTCTGAC[A/T]ACTCTAATGACTTCA | 57626 |
rs187164256 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865934 | TTTTAACATATTCTG[A/G]GAGTAACGAACATTA | 57626 |
rs187170610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004731 | TGATTGTTTTTACAT[C/T]TTTATTACACCCAAA | 57626 |
rs187172323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024835 | TGATTCCCTTAAAGA[C/T]AGTACAACATTTTTA | 57626 |
rs187172629 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828207 | CAGCTAGAAAACTGT[C/G]AGTGCCCAAAATGTG | 57626 |
rs187177839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764801 | CATGCACATTAAAAA[A/C]GTATCTATGTTCTTC | 57626 |
rs187183064 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043486 | TGTACAGTAATGTTC[G/T]TGGCCTTCACATTCG | 57626 |
rs187186259 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062079 | TTGTATTCCTTAACC[A/G]GCCTCTCCCCATCTT | 57626 |
rs187194482 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077888 | TATGTTCTGTGCCCT[G/T]TCTGTGATATTTACC | 57626 |
rs187218116 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722558 | TGAATAAATTCTCAA[C/T]AGCACTAACCATCAG | 57626 |
rs187226626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704756 | TTTTTAAAAATCTGC[C/T]TTTGTTCTCCCTCCA | 57626 |
rs187235919 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109888 | GCATGTAATTAATTT[A/G]TATAGAAATTAGTGC | 57626 |
rs187237677 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69827590 | CGAAAATTAGCTGGG[C/T]GTGGTGGTGCATGGC | 57626 |
rs187254063 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865579 | GGAAAAGATGTCACA[C/G]GAGTTTGGCAATTTA | 57626 |
rs187259450 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082797 | ATGCAGCTATAAAAA[A/G]AGAAGAGTGGAATCA | 57626 |
rs187278320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929044 | ACAGTTTTATTACTT[A/T]ATGACAAGACGGCAC | 57626 |
rs187282577 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965333 | TATTTTATTGTTATG[C/T]CTGTTACAGTAATTT | 57626 |
rs187287600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901651 | GATCAAATTTTTGAA[C/T]GTTGACCTAAATTTT | 57626 |
rs187299563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724935 | TTAATAAATATCATG[C/T]TTACATCTGCTCTAC | 57626 |
rs187312316 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69767998 | ACTATATTTACAAAA[C/T]ATCTAAATTAGTAAA | 57626 |
rs187326719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795376 | ATTAATTTTGCTTAC[C/T]TGTGAATGTCTAAAT | 57626 |
rs187327084 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728101 | AGCTGATTAGTAGCC[C/G]CAACTGAGATTCAGT | 57626 |
rs187333291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996181 | GGTAGCATGTCCCTA[C/T]AATCCCAGCTACTCA | 57626 |
rs187337486 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749296 | ATCAATATTAAAACT[A/G]CATTCTAAAAATAAT | 57626 |
rs187338932 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037125 | CCAATTTTACTTAGT[A/C]AGATATTTTTCACAT | 57626 |
rs187346735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915027 | AAATCTCTCAAGAAG[C/T]AGGGACTTATGGTAC | 57626 |
rs187354607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869222 | TTTCTGATAATAGCC[A/G]ATCCTTACTGTTTAC | 57626 |
rs187357913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104111 | TTACTACATATGGAA[A/T]CTTGGGCAGAAATAT | 57626 |
rs187362226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831759 | TCCACGATGATCAAG[C/T]TGATTTCACACCAGG | 57626 |
rs187362979 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710633 | ACTCAGGGATTCACC[A/T]CTCAGCATGGGACAT | 57626 |
rs187368362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932482 | GAAGGGAATACTACA[C/T]CTTAAATGATTGAAA | 57626 |
rs187376490 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066165 | AGCTGTGCTTTTTAC[G/T]GTCTGCACTGTGAAT | 57626 |
rs187379900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949414 | CTGATTATTAGACTG[G/T]GGTTATGAATGAAGT | 57626 |
rs187386895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982496 | AAATAAAAAGCAATA[A/C]ATCAAAACATGTTAC | 57626 |
rs187389564 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967297 | ATAAGTCATGGGAGG[A/C]AGTAAAAATAACAAC | 57626 |
rs187393808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907294 | AGTGTGAATGTTAGA[A/T]TGACAACTCAAATAC | 57626 |
rs187394745 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029394 | ATGAAGGTGAAGCCT[G/T]ATATTTGAAATTTCA | 57626 |
rs187398564 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046756 | TGGCCTCAAGTGATC[C/T]GCCCGCCTCGGCCTT | 57626 |
rs187401806 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999318 | CGAAGATCATCGGTG[G/T]TCACCTAAGTCTATG | 57626 |
rs187402877 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020186 | TAAATGGACAAAAAG[A/T]TCTATTTAAGGAAAA | 57626 |
rs187441938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909383 | AAATATTTTACATTA[C/T]ACTATTCCAAAGAAT | 57626 |
rs187448003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945457 | CTGCCTCTAGTTAAA[A/C]GAAAGAAAAAAAAAA | 57626 |
rs187492331 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099320 | AGCCTATGAGCAGTA[G/T]TCATACTTCCCATTG | 57626 |
rs187497662 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053291 | GGGAATCTTAAATGG[C/T]AAATGAGTAATATAA | 57626 |
rs187499170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005252 | TTTTAAGAAAAACTT[A/C]CATGAGCAATAGTAA | 57626 |
rs187503117 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707904 | AGGAAACTACCTTTT[A/T]TTTTCTCTAAAGGCT | 57626 |
rs187508028 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043639 | TATGCTTAGATACAC[A/T]AATAACATTGTGTTA | 57626 |
rs187510263 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070555 | AATAAAAAAATTCTT[A/C]AACAAAAATACAAAG | 57626 |
rs187523294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078900 | TGAACCCACTTAAAC[A/G]ACTAGTCCTCTAAAA | 57626 |
rs187542618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733794 | TTGAGCAGTATCTAC[C/T]AAAGCTGAGCACAAG | 57626 |
rs187550259 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69752533 | GAAAATAAAACAAAT[A/G]ACAATCGTTTGCAAC | 57626 |
rs187554575 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69917058 | GTTTGCACATGTGTA[C/T]GTGTAAGTGTATTTT | 57626 |
rs187554762 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69871356 | GGAAGGGGCTGCCTC[C/T]AGACTTTCTGAAATT | 57626 |
rs187559526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776160 | GACTCCGTCTCGGAA[A/G]AAAAAATAAAAATAA | 57626 |
rs187564659 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715822 | GTTTGGGGGAGGAAG[G/T]GGAAGGGAGAAGAAG | 57626 |
rs187567771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086053 | TACAAGTAAGTACAG[A/G]TAGGATGCCATATTA | 57626 |
rs187568542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747737 | TTTAAAGCATGACAA[C/T]ATCAAATGTTGCTAA | 57626 |
rs187572701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888909 | GAATTTCTAAGTTAT[A/T]TCTTTTATAGAGTAA | 57626 |
rs187574747 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936854 | CAAGAACCTCCAGAG[A/G]CCTCCCAACAATGGT | 57626 |
rs187575380 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754033 | TTTAGTAGAGATGGG[C/G]GTGTACCTTTGTTGC | 57626 |
rs187582242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812671 | AAATGATATGAACAG[A/G]CATTTCTGAAAAGAA | 57626 |
rs187584519 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714890 | TGAGCCACTGCACCC[A/G]GCCGATATCCTTCTA | 57626 |
rs187585898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952957 | ACAAATAGTCAAAAC[G/T]GAAGTAAAATAATGT | 57626 |
rs187595649 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909545 | GGATAATTTTTTTTT[A/T]AAAAAATCAAAAGTC | 57626 |
rs187600241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971091 | CATTATTTCAGTACC[C/T]AGATTGCCTGGGTTT | 57626 |
rs187600989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792755 | TTGACTTTAAAACAT[C/T]GTGCTACATGAAAGA | 57626 |
rs187608009 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69986055 | CCCTCCAGGATATTA[C/T]TTTAAGTAAAATAAA | 57626 |
rs187609509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003432 | AAATACATTCAATTG[A/G]TATTTTAAGCTGAAT | 57626 |
rs187612229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023946 | CCATATGACTCCATT[A/G]GAAACGTATATAGTT | 57626 |
rs187623343 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69891966 | TTTGATTTAACAAAA[A/C]TAACAAATTTCTCAA | 57626 |
rs187626871 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847689 | AATTTCATGTACTTC[A/C]TCTTATTTCATAATA | 57626 |
rs187628216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828598 | GAGGCTAAAGCAAGT[G/T]GGGAGGGGTGAGGCC | 57626 |
rs187629649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854999 | AAAACACTTATTTGT[A/G]CTCATAAATATATGT | 57626 |
rs187630262 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70087455 | ATAATACGAACAATG[C/G]CTGAAGGATTAACAG | 57626 |
rs187637674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930434 | GGTCACTTAAAAACC[A/G]AGCTTTAGAGTACTT | 57626 |
rs187646022 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69886260 | TAAGACAGGATAGCT[A/G]CAAAAATAAAGACTA | 57626 |
rs187649531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923140 | ATAAAATGGGAAGAA[A/G]GTTCATCAAATGGTA | 57626 |
rs187678257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925967 | TATAGCAGCATATCA[A/G]CAATAATCAAATACA | 57626 |
rs187697105 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991242 | ACATCACAATGAGGA[A/G]AACTAGAAAAACAAG | 57626 |
rs187704794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029804 | ATTAAAAGACACAGA[C/T]TGGCAAATTGGATAG | 57626 |
rs187707319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094482 | TGGGAAAAAGCAAAA[A/C]GTGTGTCTCATAAAA | 57626 |
rs187722048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067759 | GCTGGAATCCAGAAC[A/T]GATAATGAGACCAGT | 57626 |
rs187730037 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988089 | TAAATAGCTTTTTTT[G/T]GGCGGGGGGAACCTC | 57626 |
rs187731152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959137 | GGCATTTTTGTATCC[C/T]GTCCGCCCTCTACAA | 57626 |
rs187734627 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942798 | TTCTCCAACAGAGTG[G/T]CAATATAATTATCAT | 57626 |
rs187739499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974989 | GTCCTTCCCCATGTA[C/T]TCCAAGACACTGACT | 57626 |
rs187753632 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026260 | AAGGTATATTTATAA[A/C]TGATTTTTTTAAAAA | 57626 |
rs187756803 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991573 | ACACAAACTAGAAAA[G/T]GTAGAAAAAATGGAT | 57626 |
rs187762091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008837 | GATGTGATCAAATTA[A/G]TTAATTTTCATTGAT | 57626 |
rs187763620 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062875 | AGAAAAAGTGAAAAA[G/T]TAAATGTATTTGCCT | 57626 |
rs187767299 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073224 | CATAGAATACTATGC[A/C/G]GCCATAAAAAAGGAT | 57626 |
rs187771308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048076 | TAATCACTAGCATAG[A/G]TCACTCCAAAATTTG | 57626 |
rs187774957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837350 | AACTGTGACATTTCT[G/T]TGTGAATAATAATTA | 57626 |
rs187778633 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821841 | CTTTTTTGCTTATGG[A/C/T]CCCATTAATAGAACT | 57626 |
rs187783209 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068231 | CTGTAGTCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 57626 |
rs187793144 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801135 | ATACCCCATACATTT[A/C]TTTAAAATATAATGA | 57626 |
rs187797069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874213 | TGTGTGCCTGCCACT[A/G]CAATCCTCTCCCCTT | 57626 |
rs187801246 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738967 | AGATTCGCCAAAGTC[A/G]AAATGAAGAAAACAA | 57626 |
rs187806101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892714 | GATACTTCGGGAAAG[A/C]CTGTTATATGCATAA | 57626 |
rs187821175 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103366 | ATGGTACAGATTGTC[A/T]TCAGTTGGCGTCCAT | 57626 |
rs187831066 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098227 | ATTCAGGTGAGGTAA[A/G]TAAGGCTGACTTGGT | 57626 |
rs187831538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734867 | CATGCTCAAGAAAAT[A/G]CACTTCTCATGATTA | 57626 |
rs187842200 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914614 | GCCAGATAATGAAAC[A/G]TGATATCTGTAGTTA | 57626 |
rs187847952 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781567 | GAATTTCATTGCTGT[C/T]TCATTGCTGCTCATT | 57626 |
rs187870267 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849391 | CAATACCCTGAAGCA[C/T]GTTATTCTACATTTT | 57626 |
rs187877668 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835423 | GAATACAAAAGCCAG[C/T]ATCTCTTGTGGACAG | 57626 |
rs187878402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815393 | AAAGAATGAAATCAC[A/G]TCCTTTGCAGCAACA | 57626 |
rs187883751 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777621 | TGTTTTTACACATTT[C/T]ACTTTTTTGGCTGAA | 57626 |
rs187912491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873642 | TAACATATCAACAGA[C/T]AGGAGAAATACCTAA | 57626 |
rs187912505 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810382 | AGACATAAACACTGG[G/T]AAAGTTCTCAAACCA | 57626 |
rs187913364 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917392 | TCCATATTACATTCA[C/G]AATGACTGTAAATGT | 57626 |
rs187924142 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879510 | CTTAAAGATTATAAG[C/T]GACCTATATATTAAT | 57626 |
rs187933541 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913273 | CATTTCTCCAGCAAG[A/C]CCAAGTTTGGCTTCC | 57626 |
rs187952631 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953484 | CATGGAAAAATTAGG[A/C]CATGATTTTACATCT | 57626 |
rs187959598 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69897112 | ATACCTGATAATTTA[A/T]TTAAAAATCAAACAA | 57626 |
rs187967116 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987155 | CATTTGCTCTACTCA[A/T]GTTCACCATTCGCAA | 57626 |
rs187975410 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880212 | TCCTCTGTGTAACAG[A/C]TTTAATAATCTTTAC | 57626 |
rs187975759 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69834255 | TTAAATAAATAAGTA[C/T]ATAAATTGGGGGGAG | 57626 |
rs187979274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100084 | TAACAAAAAAGCATG[C/G]AAAGATTTTCTTCAG | 57626 |
rs187979844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938453 | GAAGAAAAAAATTTG[C/T]TACTATTGTGCGATA | 57626 |
rs187988613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008097 | CACTTTTTACAAGAT[A/T]TCTAGCTGCAAATTT | 57626 |
rs187990223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917768 | GTTTTTTGAATTTTG[A/G]TATCACATAACATTC | 57626 |
rs187998356 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954326 | GGTGGAAAAAGCCTA[A/C]GAAAATATAGTGAAC | 57626 |
rs188005753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047701 | AAATACACAAACTGA[A/T]TTTTTTTAAAAAAAA | 57626 |
rs188018407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797785 | AGTGAGCAGAGATCG[C/T]GCCACTGCACCCCAG | 57626 |
rs188018613 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700921 | TAGCTTCCATGCTTA[C/T]ACTGAACTCAACATA | 57626 |
rs188026528 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824663 | GACTACAAAATGTGT[A/G]ATTTCCATTTATGTG | 57626 |
rs188026640 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782278 | TTCCATCTGAGGTAC[C/T]GGGTTCATCTCACTA | 57626 |
rs188030008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803628 | TGACGTGATCCCCTG[A/C]AAGTGAGAGATTTTC | 57626 |
rs188031700 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719938 | TAAAATATAAGACAG[C/T]GAACATAAACAGGAG | 57626 |
rs188035915 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69760378 | TTATTATTTTGAGAC[A/G]GAATTTCACTCGTTT | 57626 |
rs188039444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741086 | TGCTTTGGTTTCCCA[A/G]AAAGGTTAAAATAAA | 57626 |
rs188043664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878077 | TTTTTGGCACTAATC[A/G]TTCTTTTAACATGTT | 57626 |
rs188054908 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816329 | GCAGTAGCACAATCT[C/T]GGCTCACTGAAACCT | 57626 |
rs188058738 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840028 | AATTTAGCATTTACT[A/C]ACTGAACTTTTCTTG | 57626 |
rs188060878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860265 | ATCTCAATGTTCAAA[A/G]AAGCAATTTCAGAAC | 57626 |
rs188070358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719296 | AATAATGCAATTTTT[C/T]CAATCACTTGAATCA | 57626 |
rs188116404 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734622 | ATGACACTGGCAAAT[A/G]CTATGACAAGATGAA | 57626 |
rs188117577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797182 | AATGTTCACCTTGTT[C/T]GAATTACATAATGGT | 57626 |
rs188140181 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759803 | CCTAAATATTGTATC[A/G]TCATTTGCCCAAACC | 57626 |
rs188154221 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901891 | CAACCTCTGCCTCAC[A/G]GGTTCAAGCGATTCT | 57626 |
rs188156926 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832982 | ACTTAAATCTAAGAC[A/G]TAAAGTCACTAAAAA | 57626 |
rs188157805 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767565 | AAAACAGTAAATATC[A/C/G]GTCTATACTAATATA | 57626 |
rs188160759 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875426 | ATTGCAGTAGTGGAA[A/C]CCCTTTGGCAAGAAA | 57626 |
rs188165957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995797 | CACCAGATGAATAGG[C/T]TAAACCTAGTTATTT | 57626 |
rs188170464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980302 | AATAATTACTCATGT[A/G]TTTTTTACTTTATGA | 57626 |
rs188172652 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837608 | TATACACATACATCT[C/G]TCTCTCTATATATAT | 57626 |
rs188176306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017126 | TCTGCATTCCTCATT[C/G]CTCCTGGACATAGGA | 57626 |
rs188181289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941472 | GAGGAAAGTTTATAG[A/C]GATAAATGCCTATAA | 57626 |
rs188184871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724533 | AAAGCCAGACAAAGA[C/T]ACCACCAAAAACAAA | 57626 |
rs188186389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823052 | TGTATTTGCTCTGTG[A/G]AGACATAGAAGCCTC | 57626 |
rs188186661 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801804 | CATTTGTAGTAATAT[A/C]AAATTTTGATACTGA | 57626 |
rs188191526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974393 | TTGTAAACAATTTGC[A/G]TAACTAAATAATTTA | 57626 |
rs188194922 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746710 | TTATTGTTGAGAGAA[A/C]GCAAATGATTGAGTT | 57626 |
rs188196838 | snp | A/C/T | 0.00994088 | 0.0698686 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785833 | AGGGGATATCGCCAC[A/C/T]GATCCCACAGAAATA | 57626 |
rs188199535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055086 | AAAGTTATAGGACAT[C/G]AAGCAGACTTAACCC | 57626 |
rs188207488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071547 | AAGCTCACATGAAAC[A/T]CTCACCAAGACACAT | 57626 |
rs188210280 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896741 | TGGTGCAATCTCGGC[A/T]CACTGCAGCCTCTGC | 57626 |
rs188214484 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70087677 | TGAGCTGGGGCTGCT[A/G]GGATTTAAAATGAGG | 57626 |
rs188215275 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007797 | AATACAAACACAGAG[G/T]TCTCTGTACCCACAT | 57626 |
rs188218273 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837632 | TATATATGTGTGTGT[A/G]TATATATATATGTGT | 57626 |
rs188222930 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69937391 | AATTTTATTCTGGCA[C/T]AGGCAGCCATTTTTT | 57626 |
rs188226924 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69971190 | TTTCTATATTATAGA[G/T]AAAAGTGAGAAATTA | 57626 |
rs188228079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095722 | TTATTTTGAGAGGAC[A/G]ATAAATTATTGTTAA | 57626 |
rs188235101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994120 | GAACTGGGAAGCTTT[C/T]ATGACCTAAAATATC | 57626 |
rs188247174 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038669 | GATCTCAGCTCACTG[C/T]AACCTCTGCCTCCCG | 57626 |
rs188267955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074123 | TGAGCCACCTTGCCC[A/G]GCACCTTAAGCCTCC | 57626 |
rs188329837 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70090605 | CCTTTTCTCACGATG[A/G]TATAGGGAGAAGAAG | 57626 |
rs188358805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718607 | ATCATTATGTATCCT[A/G]TGTAATAGGAAATAT | 57626 |
rs188359566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868991 | TTCACTCACTTTTTA[A/T]TTATGAAAAAATCAA | 57626 |
rs188359988 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70093723 | CTTTGTTTTCTCATG[A/G]TATTTTGAACCAACT | 57626 |
rs188367780 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885650 | ACTCCTTATTGTCTA[C/T]GAAGATCATATAACA | 57626 |
rs188392750 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715581 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 57626 |
rs188396099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788680 | AATAATAGAAAATAT[A/G]GTATTTATGTATATC | 57626 |
rs188401503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923047 | AGACAGAAGATGGAA[G/T]CAAATGCAACCCTCT | 57626 |
rs188403286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906145 | CATGAGAACTATTCA[C/T]TTATTAAGTAATTAC | 57626 |
rs188404469 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861021 | CGGTGAGTTATGATC[A/G]CAATACACAGACAAC | 57626 |
rs188407220 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960161 | TGAGTGTTATCTTAG[C/T]GTTAGCAAATCCTTC | 57626 |
rs188413995 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001604 | ATCTATCTATCTATC[C/T]ATCTATCTATCTACC | 57626 |
rs188415179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822625 | AAGGTATAGCTCCAA[A/T]TGAGACACTTACAAA | 57626 |
rs188417246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943703 | ATAGAGAAAATAATA[C/T]AAACACATTAAAATC | 57626 |
rs188427417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021307 | TCACTAATATGCATT[A/G]AAGTGTCTTGCATGG | 57626 |
rs188429279 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976142 | AATTAATTAGCAATG[A/T]AATGTTAATTTCGTT | 57626 |
rs188430475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729204 | TTCTTTATTCACCAA[A/G]TGAGTCTGGCTGTGC | 57626 |
rs188437261 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992366 | TAATAATGACCAAAA[G/T]AACTAACTGATAAGT | 57626 |
rs188442519 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703209 | AATGGAGCTGAAAAA[A/T]TCCATCGTCTGGTAA | 57626 |
rs188446438 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721402 | CATTGTCAGGTCTCC[C/T]GAGGCTGTGTAATGG | 57626 |
rs188446543 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896297 | TCCTCTTCTGCTTTT[A/G]CAGACTCATGCCGCT | 57626 |
rs188449849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921501 | AGTGCTCCAGATCCA[C/T]GCAATCAATCTTTCT | 57626 |
rs188455472 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69883817 | CAAAAAGTCTTCTGT[A/G]GATGATACATGTTTA | 57626 |
rs188461461 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108724 | CATGAATCATGGCAG[C/T]GTAAACTTAATAGGC | 57626 |
rs188472141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091970 | AGGGTGTAGTGGGGA[A/G]CATCTACCCATATAT | 57626 |
rs188474672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927670 | GCTCAGTTTCATTAG[A/G]CATAGGAAAATCACA | 57626 |
rs188478837 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69964278 | AGCTACTGGCCTTGA[G/T]TAATCCTCCTGCCTT | 57626 |
rs188487032 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69955870 | GAGAAAATACTAGCA[A/T]ATATATATTTATATA | 57626 |
rs188488932 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991049 | CAACGTGCTTCTGAA[A/C]GATTCTTGAGTAAAT | 57626 |
rs188495622 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69994819 | GAGGAAAAATTTTTT[A/T]AAAAAATACTAATAT | 57626 |
rs188513979 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70061703 | AGGCTTATCTCAATT[C/G]TCTTCTCTCCACTCC | 57626 |
rs188514347 | snp | C/G/T | 0.00954511 | 0.0684907 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035286 | TCATTTACAACAACA[C/G/T]GGATGGAACTGGAGA | 57626 |
rs188544623 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058231 | ATCGTATTAGAAGTG[C/T]TCTCTAGAGCAATCA | 57626 |
rs188577777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028224 | GTAATACCTTTGTTA[A/G]GAATTATAATTTGAT | 57626 |
rs188585422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705353 | TAAAACAAAAGCACA[A/G]AACTGTTAATCGATT | 57626 |
rs188586553 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700100 | TAATCATTGATATTA[C/T]CCTATTATTTTTTAG | 57626 |
rs188589183 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70044942 | ATGACTCACAGAATA[A/C]CCTTGGGAAAGTCAT | 57626 |
rs188601345 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064045 | AAATACTTATTATCA[A/G]AATTGATTATCAAGC | 57626 |
rs188602966 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107873 | GGCGAAGGCTGGAGC[A/G]CAGACGGCAAAGCCG | 57626 |
rs188607771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081575 | CATGGAGATCTCTCC[A/G]TTGTTCTTCTTAAAA | 57626 |
rs188608928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842595 | TGTTTGTTGGAAGGT[A/G]AACTAGTAAAGCCAC | 57626 |
rs188614183 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102790 | TAATTTTAACTTACG[C/G/T]ATATAAATATTCAAC | 57626 |
rs188621788 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70103605 | TTAGGCGCAGACAAT[G/T]GCTGTGAAGAGATGT | 57626 |
rs188628178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086750 | TTATATGTAGTGCCT[A/G]CAGGCAGGCAAACTA | 57626 |
rs188628590 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785137 | GACCTCGTGATCCGC[C/T]CGCCTTGGCCTCCCA | 57626 |
rs188631967 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881514 | AGTTAGGGTCACCTT[C/T]AAGCTTATTTTTGGA | 57626 |
rs188634586 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809784 | AAATAACAAGACCCA[C/T]CCTTCCACTGTCTTC | 57626 |
rs188639334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772306 | TCTTCTTCAAATAAA[A/G]CCAAAAAGAAATTGT | 57626 |
rs188642354 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889528 | GTTCTCCTCACCCAT[A/C]TATTTTGAGCTTAAT | 57626 |
rs188644173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724176 | GTATGACCTGGAAGT[C/T]CCCAATTTTGCCTTG | 57626 |
rs188646378 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927954 | TTCATAGCAGTCAAG[C/T]TATCCTCACAGGATT | 57626 |
rs188647752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738248 | ATCCAACAGTCAGCA[C/G]CTTCAAAAATCAAAG | 57626 |
rs188650114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910457 | CAACAAGGGTTTTCA[A/G]TTGTTTGTTTATTCA | 57626 |
rs188651075 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863573 | TCTTTTATATTTGAA[C/T]TTATGATTTTTTTTT | 57626 |
rs188654537 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69746376 | GAATTGATTGTTAAA[C/T]ATTTCCTTTTATTTA | 57626 |
rs188655252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964867 | CTCTTGGTCAATTTC[C/T]ATTGACTGATTTTTG | 57626 |
rs188657824 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69746154 | TTCTTATGTATTGAC[C/T]ATATCCAGTAGCCTT | 57626 |
rs188659273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947391 | ACTTCCCAGATCAAC[A/G]CTTGAAAAAAGATCC | 57626 |
rs188665206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978952 | GAAAAGAAAGAAATA[C/G]AGCTTGGTGAGACCC | 57626 |
rs188668663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804622 | CTCACAAAGTAGAAT[G/T]ATTTAGGATAATTTA | 57626 |
rs188681836 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706286 | CTTTTTACTTACTTG[G/T]CTAAATGTACCTATT | 57626 |
rs188687120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995205 | CACTCCCAAGGCCTA[C/T]ACTATTATTTACTAT | 57626 |
rs188692319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878419 | GCCATTTACATCTGC[A/C]GGAATTACCTTACAA | 57626 |
rs188696784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840736 | TGTATGTATGTATGT[A/G]TAGAAGATCTCCAAT | 57626 |
rs188734570 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69949115 | ATTAACATCTTACAT[C/T]CGTATGATATACGTG | 57626 |
rs188744749 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922170 | CAGGCTGGTCTCTAA[C/T]TCCTGGTCTCAAGGG | 57626 |
rs188749310 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981945 | TAAAATAATAACTTT[C/T]TTTCAGAAATAGGCA | 57626 |
rs188750061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946316 | TTTGTATATGTGCAG[C/T]TTATTATATCTTGAT | 57626 |
rs188759037 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019643 | CTATTTTACAAATGA[A/T]GAAATTGAGCAAAAG | 57626 |
rs188779058 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70057435 | TCATTCTGAGGCCAG[A/T]ATGCCCTGATATCAT | 57626 |
rs188783776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978073 | CAAGTTCGCAAATTA[A/C]AACCCCAGAATATGG | 57626 |
rs188784970 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043132 | CTGATCTCGAACTCC[C/T]GACCTCTGGTGATCC | 57626 |
rs188793111 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015072 | CATGATCAGAATTCA[C/T]ATTGAACTGAAAGTA | 57626 |
rs188803214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077801 | AACATTTTAGAAACA[C/T]ATTATATACACAAAA | 57626 |
rs188808333 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915796 | GAAACTACCATCAGA[A/G]TGAAAAGGCAACCTA | 57626 |
rs188808567 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69951827 | CTTGAAATCTTCACA[C/T]CTCATAATCCATATT | 57626 |
rs188827078 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69969113 | ATTTTATCTTACATA[A/T]AAGGTAAGTGGAAGG | 57626 |
rs188830432 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778775 | TGTATATAATATTGA[A/G]GGCAGGTATTCCCTC | 57626 |
rs188837028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984536 | AGGTAAATGTCACAC[C/T]TGGTCCAACCAATCT | 57626 |
rs188839161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002629 | AACCCCAATCAGGAT[A/G]TATACAACATAAACC | 57626 |
rs188839271 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:70049963 | GAAAAAAATGAAAAA[C/T]GAATCAGACTAATAG | 57626 |
rs188843520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021876 | GCTTTAAGGGTTCTT[C/T]GTATATTTTAAAAAC | 57626 |
rs188846473 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068327 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 57626 |
rs188851326 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727327 | TGGGTTTGTTTATCA[A/G]TCTAGAGAGTTTTCA | 57626 |
rs188858396 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041126 | TACCTTTGCTCATTT[A/T]AAAAAATTTTTTTTA | 57626 |
rs188859362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830162 | AAAAAATACGGAATG[A/G]ATAATAATTCACCAA | 57626 |
rs188864931 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811177 | CAACAGTAACAACAA[C/T]GAAACTACAGGCTAA | 57626 |
rs188868021 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100504 | ATTCAAATAAAAAGT[G/T]TTGTATTTTTAGTAG | 57626 |
rs188871464 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794707 | AACCACTAAGAAGAA[C/G]AAAGCAATTATAATG | 57626 |
rs188875186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105794 | CCTAACGTTATAATT[A/C]TTTTTCCTAAAATAT | 57626 |
rs188876702 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723834 | TTCAGCCAGTTGCCA[G/T]TCAGAATTTTTTTTT | 57626 |
rs188883802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771092 | CCATATATACTTTTG[A/G]GCTTTACCAACCTTT | 57626 |
rs188889454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845922 | TAAAAAGTCAATATT[C/T]GAGGTTTGCCTTGTT | 57626 |
rs188895320 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69867861 | CTGTTGTGGGGTGGG[A/G]GGAGGGGGGAGGGAT | 57626 |
rs188899797 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085819 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 57626 |
rs188916497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767034 | CAAAGTAGCAATTGG[C/T]ATTTTTCTAGAGTTT | 57626 |
rs188922735 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791439 | TAAACTGATCTTTTT[A/T]AAAAAAATATGGAAA | 57626 |
rs188936144 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833543 | ACTATATAAAAAACA[C/G]TATGGAGATTCCTTA | 57626 |
rs188972373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871115 | CTGCCAAGCTTCCAC[C/T]GCTTTTCCATTGTGG | 57626 |
rs188981133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872022 | CCGTATCAATTTTCT[A/G]CCTAAGTCTGTTTTG | 57626 |
rs189000143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931246 | ATCTAGCCTGAATAT[C/T]TACTCAGTGTTAAAT | 57626 |
rs189004006 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69910969 | TTTACACCTCTATAG[A/G]CAAGAATAATCTGCA | 57626 |
rs189011334 | snp | A/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69967059 | ATATTGTGAATAGTG[A/G/T]TGCAATAAATATACA | 57626 |
rs189030064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947801 | TCATGCATGCTGTAT[A/T]TCTCGGCCAGACCTA | 57626 |
rs189032175 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971971 | CAAGTGATCAAGAAA[A/G]CAAAAGTTTTTCAGT | 57626 |
rs189035368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998363 | TGGGAGCTCCCATTG[C/T]GTGGGAGCACAATTA | 57626 |
rs189048042 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954556 | ATTTTTCTTACTTCA[A/T]AACCCAGAAAATAAC | 57626 |
rs189053820 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038314 | ACCTGTTGAAGGGTA[G/T]CTGGACTCTTCCATG | 57626 |
rs189062266 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69972713 | CCCCATGTATGTCTG[A/C]AAAATGCTCTTACTC | 57626 |
rs189073698 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751329 | TTCTATAAGTTCATA[A/C]CCTCACAGAACGCGT | 57626 |
rs189077881 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782427 | TCAAAGAAAGGGGTG[A/G]CAGACGGCACCTGGA | 57626 |
rs189078755 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70005689 | CTTATTTCGCTTTGA[A/T]TAAAATATCTTATAT | 57626 |
rs189078987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988367 | TCCAGCCTATGGTTG[C/T]TTGGCATTTAGGTTG | 57626 |
rs189093155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027154 | TTTTTAAAAATATTA[A/T]AATAAAACTATTACT | 57626 |
rs189101457 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044164 | CTTACTACTTCTCAC[A/G]GCCCAGTTCATACTG | 57626 |
rs189109826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713608 | TGTGATAAACTCACA[C/T]TGGATTTATATACAT | 57626 |
rs189112750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774021 | AATTGTGTTAACTAA[G/T]TTGTTGTAAAAATAA | 57626 |
rs189112813 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730134 | TCCATTTATTTCTGA[C/T]TAAGATTGGAGAATA | 57626 |
rs189114639 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816998 | AAAATAAATATAATA[A/T]AAAAAGCTTTACAAC | 57626 |
rs189116737 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798070 | TCATTAAAAATGCCT[C/G]TGTAGAACAAGCTCC | 57626 |
rs189123072 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709217 | CAGATAGATGCAGAC[A/T]TACATAGACACACAC | 57626 |
rs189134171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850691 | AACTACTCCCACAGC[A/G]TCCTAAAACATACAC | 57626 |
rs189157153 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788580 | GATGAGTTAATGGGT[A/G]CAGCACACCAACATG | 57626 |
rs189167602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088961 | TATATTTGAAATCAC[A/G]TATTTATTTTATTGT | 57626 |
rs189188845 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69748701 | TTTGTGTGAAGATTA[A/C]ATAGAAAATGCAGAT | 57626 |
rs189193826 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69911111 | GTAATCAGTCTGTCT[C/T]TCTCTCTCTCTCTTC | 57626 |
rs189214277 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849990 | CTCTTTGCTAAACAA[G/T]CAACCAAATATCTAT | 57626 |
rs189225347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856316 | GCATCCTGTTACACA[C/T]ACAGGTGTCACTTGG | 57626 |
rs189227454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831291 | TAACACAGAAATAGA[A/G]AAGATCAGACAGGAC | 57626 |
rs189237521 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888453 | ATCTAATGACTGTGG[C/T]CTTTCTAAGAGAAAT | 57626 |
rs189242033 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795174 | TGAACCTTTTATTGG[A/C/T]GTGTAAATCAAAGGC | 57626 |
rs189258171 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838537 | ATAAATTATAACTTT[C/T]ACCATTCTTATACTT | 57626 |
rs189261739 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857377 | TGCCTCAAATTTACC[G/T]TCAACATGTAGTCGC | 57626 |
rs189262698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852321 | CTTCCCTTACTTCTC[C/T]CACATTTTATTTCAG | 57626 |
rs189268381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071845 | GTACATACAGCAAAA[G/T]TGGAAGTATGTCTAT | 57626 |
rs189271719 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823533 | GACTAGATGTATATA[C/T]ACACACATATAGCAC | 57626 |
rs189275116 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894411 | TGTCTTGTGGCCATA[A/C]CTTTTACATCTCCCC | 57626 |
rs189282325 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69933804 | GAGAAGGGGGAAAAA[A/C]AAATACTTGAGAAAA | 57626 |
rs189285350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915453 | GCATATCTACAACTA[C/T]CTGATCTTTGACAAA | 57626 |
rs189288205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967525 | CAAAGAAAATGATTC[C/T]TGAGATGGTGTCTAC | 57626 |
rs189289397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876866 | AGTGTGGCAAAACCC[C/T]GTCTCTATTAAAAAT | 57626 |
rs189295987 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69928840 | GTGATAGTGGTGATA[G/T]TTGCACAACTCTGAA | 57626 |
rs189304305 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889914 | CCTTCCCTTCAGCCT[C/T]CTCTTGCTAGCTCTA | 57626 |
rs189305169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933965 | ATATTCATTAGCATA[C/T]TGAATAGGGCATGAA | 57626 |
rs189322914 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755271 | GATACACCAGCTTCT[C/G]CTTTGGGATGAAGGA | 57626 |
rs189330854 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964994 | CTAAGAAGGGAGCTG[G/T]CCTTTAGTTCTTAGG | 57626 |
rs189345570 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70031725 | ACAGGCACAAAGGCT[A/G]TTTGATTGGAAGCTG | 57626 |
rs189349184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794622 | CTACAATAAAAAAGA[A/G]TTAAAGAAGCAGATA | 57626 |
rs189355548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778132 | GATTTAAAATGCAGC[A/C]AAGGATGAGGTTGCT | 57626 |
rs189360278 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068600 | GGGTATGCACATGCT[A/G]CAGTGTGTAAAAATG | 57626 |
rs189364698 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735282 | TGATATCAGAGACTA[G/T]AAAGCACTATAAAGG | 57626 |
rs189369313 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104222 | AATTAATGATTAATA[A/G]GCCAGTGAACTATTA | 57626 |
rs189379618 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100342 | TGTTAATATATAGAA[A/C]TACAATTGAATTTTG | 57626 |
rs189393956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711963 | TTTGCATTTCCCTGA[C/T]GACTAATGCCATCCA | 57626 |
rs189425037 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707345 | TTTATTTTTTGCTTC[A/G]GGTAACTCAAATTCA | 57626 |
rs189428299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741849 | TCATTAAGATATTCT[A/G]TCTCCCAGACTCCTG | 57626 |
rs189446900 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783045 | TGTTTTCCAGCCACC[A/G]CTGCTGATACCCAGG | 57626 |
rs189475707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763380 | GGTTTGGTTCATGGA[C/G]ACTTTTGCTAAGGAG | 57626 |
rs189483404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817724 | TCTACTAAAGGAGAT[G/T]TAGTGTGGAGGAAAG | 57626 |
rs189498490 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841585 | ATAAAAAAAATCCCA[C/T]GCTCACAGATCAGAA | 57626 |
rs189500439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819021 | TTCTTTCTCAAAGCC[A/G]TAGGATGATTACTAT | 57626 |
rs189504439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862484 | TCTTAAACTTTGGTT[G/T]GTTGTCATTAAATGT | 57626 |
rs189505160 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012067 | CACTATCACAAAAAC[A/G]GCATGAGAAAGACCC | 57626 |
rs189506691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742632 | GTTCCCAATAAGTAA[A/G]TATGCTTCACACATA | 57626 |
rs189511808 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812570 | AATGTTTGCAATCTA[C/T]TCATCTGACAAAGGG | 57626 |
rs189511974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032414 | ATTTCAGGATAAAAC[C/T]TGACAGAAAACAATG | 57626 |
rs189515159 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783226 | TGACAAAGATGGGGA[A/G]AAAACAGAGCAGAAA | 57626 |
rs189516681 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851012 | CTCCACTGGACTAGG[C/T]CTTATCTTCAACATG | 57626 |
rs189522383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051372 | TTGATAATTGCCTTC[A/G]GCTTTTCAGGTTTTA | 57626 |
rs189528695 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108541 | GATGGAGGGAGGGAG[A/G]GAGGGAGGGAAGGCT | 57626 |
rs189530240 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069054 | TAAACTATTTTGCCA[G/T]AACTAACCTATTGAG | 57626 |
rs189536345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091588 | TCTCAACAGTCCAAC[C/T]AATTTAATCATTCCC | 57626 |
rs189547412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876125 | ATTTTTGCAGCTAGC[C/T]TTGGAGACACTTATC | 57626 |
rs189555443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847572 | TAAACATATTATAGA[A/C]CAAAGAAAAAGTACT | 57626 |
rs189557417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949639 | ACTCTATCTCCATGA[A/C]GGTGGAATAACTGGC | 57626 |
rs189569360 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69920100 | CAATTTACAATATTG[A/T]ATTATTATAATTCTC | 57626 |
rs189583734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954932 | TATTTTTATTACTTT[A/T]ATTTTGTTACTGAAT | 57626 |
rs189583886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989018 | CTTTTAGCATTTTAA[C/T]GATGAAATCTTTGAG | 57626 |
rs189588526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983669 | CTACTCAGGAGGCTA[C/T]GACAGGAGGGTCGCT | 57626 |
rs189595427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106103 | TATATACACATATAG[A/G]TTATACATATATAAT | 57626 |
rs189600700 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054362 | AAGTGTCCAGTATAC[A/C]CTATTATGTTTCTAG | 57626 |
rs189614746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011402 | TACCTGGACCAGATA[A/G]TAACTCATTTTGAGT | 57626 |
rs189633957 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998283 | GTAGTAGAAATATTA[A/G]TGACTGATAGGAATG | 57626 |
rs189637045 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051087 | AAATGTCTAAATCAC[A/G]GATTTCTACAAAAAT | 57626 |
rs189653603 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70019331 | AGATACTGAATGCGG[A/G]AGGAAGAAGAATCAC | 57626 |
rs189653814 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70037996 | TTTCTGTACTTTCAT[C/T]CCACTAACAAAGCTC | 57626 |
rs189668545 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056932 | AGGAGCAAACCAAAC[A/C]CAAAATTAGTAGAGG | 57626 |
rs189674876 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073034 | AGAACTAGAAATACC[A/C]TTTGACCCAGCCATC | 57626 |
rs189676441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835497 | CACAAGGCGGGAGAA[C/T]AAGGAACCAGAGATG | 57626 |
rs189680685 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864502 | ATAAGTTTCAGCATG[C/T]ATTGCTGTGAATTAA | 57626 |
rs189689292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881678 | TTCTTATTAATTTTT[C/T]TGTACCCTACTTAAC | 57626 |
rs189704285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920732 | GTGAAAAATGCTCTC[A/G]TTCAAAGAAGTTTTC | 57626 |
rs189713607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939905 | ATGGTACGCTATAGT[C/T]CATAACAAAAAAATG | 57626 |
rs189715738 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855111 | GAGCGTATTAGAAAA[A/T]AATATGCTAAAGTTG | 57626 |
rs189715935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735816 | GTTTAAGATGACTTT[G/T]TAAAATCTGAAAAAT | 57626 |
rs189717658 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900143 | ATACTCTGGATATGG[G/T]TTTGCCTCTATGCCC | 57626 |
rs189724013 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767517 | GCCTGGGTAACATAC[A/C]GAGAACCTGTTCCTA | 57626 |
rs189729460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955139 | ATTCATGCCACTTGA[A/T]TTAAACCAGTAATAA | 57626 |
rs189730550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762732 | CATAAGTTAAGATTT[C/T]TCTGCCATCATGAGA | 57626 |
rs189747494 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973682 | AAAGTATCAGTAAAG[C/T]AGTATCAAATACCTG | 57626 |
rs189758308 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717541 | CCAACATAAATGTAT[G/T]CCTAGACTGAATTAT | 57626 |
rs189759962 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69801579 | ATACTATAATTTAAT[A/C]AAATCTAAAAGAATC | 57626 |
rs189764901 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798545 | GGATAAAAATAAATT[A/G]CAATGTTCACAAAAG | 57626 |
rs189773514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871544 | GCTCTGTTTCCCTTT[C/T]TACTATAAATTCCAC | 57626 |
rs189791618 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69834051 | AGGACACAAAGTCAT[A/G]AGAACAATACAATGG | 57626 |
rs189832948 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943021 | GTGAAGAATCCATAC[G/T]AGTTGTTCTGCAGAA | 57626 |
rs189833042 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904534 | TTATTCCCATTAGCC[C/T]TGGTACTATATAAAG | 57626 |
rs189835483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899072 | TAGAGTTAGCTAGAA[G/T]AAAGAAACACAAGCC | 57626 |
rs189838696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888134 | AGCATTTTCTTGCTG[C/T]ATTCTCATATGGCTG | 57626 |
rs189839699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939645 | TTGCCTGTTAAGTGT[G/T]CATAAAGCCATAAAG | 57626 |
rs189846988 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908782 | GCTGAACAGAATAAT[A/G]AATTCCTTTTTTATC | 57626 |
rs189857302 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110344 | CTTGGGAATATATTT[A/G]AATAAAATTCAACTT | 57626 |
rs189862430 | snp | A/G | 0.00551492 | 0.0522211 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975805 | GGTTGATGACAGCCT[A/G]TAAACCACACACACA | 57626 |
rs189864094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035412 | TGAGGATAGAGAGTA[A/G]AACAATGGTTTCCAG | 57626 |
rs189867137 | snp | A/T | 0.0520825 | 0.152737 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010902 | CGTCTCAAAAAAAAA[A/T]AATAATAATAATAAA | 57626 |
rs189876252 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962800 | AGCCTCATAATATGA[A/G]CTGGGAGCTACAACT | 57626 |
rs189884689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070645 | AAAATCATACAGATA[A/G]TAAATTCAGGCCTAC | 57626 |
rs189885649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944949 | AAATGGATCACGAAG[A/C]TAAATTCAAACATTA | 57626 |
rs189887544 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69977768 | GCAAAATAAAAAATT[C/T]GGAGAGCCTTACCAG | 57626 |
rs189902002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788376 | GGGACATGGATGAAA[C/T]TGGAAACCATCATTC | 57626 |
rs189902547 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041573 | TATACTACTGTGCCT[A/G]GAAGGGGTAGTGTAA | 57626 |
rs189905067 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096246 | ATGGTAGTTCTATTT[G/T]TAGTTTTCTGAGGAA | 57626 |
rs189908423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994154 | TATCTCTAGTAGCAT[C/T]GGGACAAGCATATGG | 57626 |
rs189908809 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770353 | AACAAAACTCATGCA[G/T]AAGCTTTGCTGGCCA | 57626 |
rs189911708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060718 | GGGCATGGTGGTATG[C/T]GCCTGTAATCCCAGC | 57626 |
rs189915900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013312 | GGAATGCAGAGAACC[C/T]GTCAGCAAATACCAA | 57626 |
rs189919568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075062 | AGATTAATAGGAAGA[A/T]AAGGCATACAAAATT | 57626 |
rs189921880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076865 | AGTAGGGTATACACA[C/T]AGGAAAATAGATTCA | 57626 |
rs189927023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748578 | AGATGAGATTTGGGT[A/G]GGGTCACAGAGCCAG | 57626 |
rs189929032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824583 | AATTAAAAAGAAGAT[A/G]GGGATATGCACAACA | 57626 |
rs189931085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838900 | TGTCATTTTTTGTAG[C/T]ATCACCATTACAATA | 57626 |
rs189946842 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803230 | TTGCTCTAAGAGCTT[C/T]ACCTACATTACTACA | 57626 |
rs189953125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720412 | TTTGAATGGTTAGGG[C/T]GTGTCACACATTGTT | 57626 |
rs189963211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716792 | TACTGTAAGCTCTGT[A/G]TAGCATAGTGCCAAA | 57626 |
rs189970640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859198 | TGACTGGTGTATCTG[C/T]TCCCATTCTTCTTTT | 57626 |
rs190001177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761989 | TTCAAGTATATTTCT[A/G]TTACCATTTGATCGT | 57626 |
rs190015693 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790060 | TCTTGGTGTTAGCCA[C/T]TTCTGACACATTTGG | 57626 |
rs190018409 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69785302 | GAAATTATAACGAAC[G/T]GTCTCTCACACCACA | 57626 |
rs190027401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756015 | CCTTGCCATTGGGCC[A/G]TTAGTGGAATTTATT | 57626 |
rs190043585 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69797752 | GAGAATGGCATGAAC[C/T]CGGGAGGCGGCGCTT | 57626 |
rs190057724 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826712 | ATATTCAAAGTATCA[C/T]GTTTTAAACCTTAAA | 57626 |
rs190067783 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69922334 | TAGAAGAGAGAATAA[C/T]GTGTAAGGACACAAA | 57626 |
rs190070249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898285 | CCTGCAAACTTTTAC[A/G]TGGACCTCAGGACTG | 57626 |
rs190076360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863037 | TGTATTGTTAGCTAT[C/G]TTTGAAGATTTTTCT | 57626 |
rs190101532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959290 | CCATGGAGCCTGGAA[A/G]TGTTAGGTTGTTAGA | 57626 |
rs190108920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991664 | GGAATCAGTAATAAA[G/T]AGCCTATCAACCAAA | 57626 |
rs190109465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929382 | AAAAAATTTAAATAA[C/T]TGAGGTAAAAATAAG | 57626 |
rs190124831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965403 | GCGGTGTCATAAACT[A/G]TACCTATATCAGACA | 57626 |
rs190126093 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948707 | GTGAAGTTTATAGAA[G/T]AATATGTATCAATGT | 57626 |
rs190132545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981395 | AAAGCAGTTTTTTTT[C/T]CTAAGTGATAAGAGT | 57626 |
rs190136664 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966289 | TTTAAATAGAAGCCA[A/G]TTCTCATTACCATTC | 57626 |
rs190140894 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997900 | GACTGCTGAAAATAA[C/T]AGTGCAATAAACATA | 57626 |
rs190149267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790787 | AGGCAAGGTGGCTCA[C/T]GCTTGTAATCCCAGC | 57626 |
rs190157957 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774762 | CTTGTATATTAACTT[G/T]GCAGAATCTGTTGCT | 57626 |
rs190158531 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996213 | GAGGCTGAGGCAGGA[C/G]AATCGCTTGAACCAG | 57626 |
rs190158848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018567 | CTAGGTGACTTGTTG[A/G]ATGACTGTGCTGTTT | 57626 |
rs190164628 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063685 | AGAAAGAAAGAAAAA[A/C]ATCAGGGTAATATTG | 57626 |
rs190165726 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060516 | TTTGGAAGGAAAACC[G/T]ATTTGTTAACAGACA | 57626 |
rs190171724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704846 | ATGAAATAAAAGTAA[C/T]GCTGAATGTAGATAT | 57626 |
rs190172668 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037403 | TGAGAACTCAATATT[A/G]GTATTGCAATTCTGG | 57626 |
rs190178458 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69751705 | TATCCTAAGAGTAAT[C/G]TGAAGTTACTAATAT | 57626 |
rs190181130 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103970 | GCTAAAACCATGGGA[C/T]AAAATGACTGCACTC | 57626 |
rs190182465 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69827243 | GCATATTTAATTTTG[C/T]CAATTATATAATTTC | 57626 |
rs190186491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808733 | AGAATGAAATGTCTG[C/T]AATGACAGATATAGA | 57626 |
rs190186691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723178 | GACTGGAGAGAACTA[A/G]TGGGGAGGGGTAGAT | 57626 |
rs190193156 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744662 | CCGAAAGGTACACCC[A/C]CCCCAAAAGCTAACC | 57626 |
rs190198175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69701920 | AAACACTGAAAATGG[A/C]ATTTTAAAAAAGCCA | 57626 |
rs190242348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707932 | GCTCAATCATTTGAG[A/C]AGGTATTCTAGAATG | 57626 |
rs190256667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747752 | TATCAAATGTTGCTA[A/T]GAACATTAGGAATTG | 57626 |
rs190266411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741455 | CTGCCACAAATTTAT[A/G]CATATTGATTAAGAC | 57626 |
rs190282057 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70105119 | TCAATAGTTTACACA[C/T]GCCTAATCTCATAAG | 57626 |
rs190288357 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70087939 | GGGCATAGGGAAGGG[A/G]GAGCATCATGATAAA | 57626 |
rs190295436 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845643 | TACATTTTATAAACA[A/C]ACAAAAAATGAGATA | 57626 |
rs190299331 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842028 | TCTGTCACCATATAC[A/G]AAAATCAACCCAAAA | 57626 |
rs190301569 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69786011 | GAAATTGTGGCAATA[A/C]TCAACAGCTTACCCC | 57626 |
rs190306812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807991 | GGAGATCTAAACCTT[G/T]GTGTGGATTGTCCCT | 57626 |
rs190307924 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69810960 | AGACTAATAAGTAAG[G/T]AAACTGAATCAGCAT | 57626 |
rs190308229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814320 | TATAAAACACTCTTC[C/T]AGACATTTGCCAATA | 57626 |
rs190310337 | snp | C/T | 8.23608e-05 | 0.00641667 | missense | KLHL1 | GRCh38.p7 | 13:69796890 | ACACCAAACTGCAGC[C/T]TTCTGCCATTCATCA | 57626 |
rs190316770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881314 | CTTACTGTTAATACT[C/T]CATACTTGCCTACTG | 57626 |
rs190329701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848424 | TAGTTCCTCCTCTTA[C/T]ATTTAAAGTCCCTTT | 57626 |
rs190330518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047191 | TTTCATAAAAACACA[A/G]TATTGTAGATATGAA | 57626 |
rs190338674 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067061 | AAGAGAACGAAGTCC[C/G/T]GTACTCCAGTTTCCG | 57626 |
rs190342001 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832438 | CTACAAAACACTGCT[G/T]AAAGAAATCATTGAT | 57626 |
rs190356064 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69908332 | AAGATGCAGATTAAA[A/G]TGTAAGTTTCACTTA | 57626 |
rs190356222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918869 | CATCTTTATAAAACA[C/T]GGGTTGTGTAATTCT | 57626 |
rs190368735 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870169 | TACAAGAGGCATGGC[A/G]TGAGCATCTGCTTTA | 57626 |
rs190370769 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887578 | TGCCAAGTGTTTTGC[A/C]ACTCACAAGTTCTTC | 57626 |
rs190384029 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950748 | AGAGATAATTCAATT[A/C]CCTTTAAAATAATTG | 57626 |
rs190387007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984044 | TCAGACCTGAAACCA[C/T]AAAATTATTAGAGGT | 57626 |
rs190399748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980977 | TTTCCATACACCACA[C/T]AGATGTGTTGCTCAG | 57626 |
rs190409743 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018050 | TTAAATAGAACTAGC[A/G]CAAAAAAAAGTTGAA | 57626 |
rs190416051 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021640 | ATCAGCAATGAATGA[C/G]AATTCTTCTTCTTCC | 57626 |
rs190419970 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70080579 | TGTTCTATCATTTTA[A/C]TCTATTTATTTTACT | 57626 |
rs190423161 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055320 | TATCCTAAAAAAGTA[A/T]ATAATTTCCTTCAAA | 57626 |
rs190428873 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708280 | GCAAAAATAACTGTA[C/G]TGTTTTGTTGTTGTT | 57626 |
rs190429670 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059601 | TTAAGAGACAAACCA[C/G]AGAATGGGAGAAAAT | 57626 |
rs190432798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726449 | TTTTAACGTGCTTTA[C/T]AGGACAGTGAGTGGG | 57626 |
rs190436361 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769616 | TAGCTAATGAAATGC[C/T]GCCTTTTCCAAGGCT | 57626 |
rs190437746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087343 | TCCAGACCACATAAT[A/G]GGTAAAAATACATAA | 57626 |
rs190442698 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748259 | CGCTTGTATCAGTCC[A/G]TTTTCATGCTGCTGA | 57626 |
rs190444193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082855 | TGGAGCCAATAACCT[A/G]AGCAAATTAGCATAG | 57626 |
rs190497577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724939 | TAAATATCATGTTTA[C/T]ATCTGCTCTACTTAT | 57626 |
rs190500465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729735 | GAGAAGAAAAAGATG[C/T]CAAGTAAAAGCTCTA | 57626 |
rs190520475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715275 | GGAGAAACTTGGTGG[C/G]GGGTGATTGGATAAT | 57626 |
rs190527944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102459 | AGAATTTTTCCATCA[C/T]TGTCAATTTAAGAAG | 57626 |
rs190534655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084954 | TTTTGGAAATAAAAT[A/G]TAGGAGAGTTCAATT | 57626 |
rs190536418 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802240 | CATGGTGTATATGTG[C/T]CCCATTTTCTTTATC | 57626 |
rs190540025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806591 | ACTGAGACCCTGGAC[A/G]TGGGGAAACAATAAG | 57626 |
rs190542877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828954 | CCTGCACCCACCAAG[A/C]CTTTCTCTACCTGCT | 57626 |
rs190548960 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776788 | ATAACAGAAATTGAG[G/T]TGGTAACTTCTGTAG | 57626 |
rs190554174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773355 | GTCTGATCAAGCATC[A/C]GTACTCTGTGAATTC | 57626 |
rs190559521 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768625 | ATACTGATTCTGCAT[C/T]GTATTTAATTTACTT | 57626 |
rs190570116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003549 | CCTTTAGAGATTCTT[G/T]TTATGCTTGAAAGCA | 57626 |
rs190573865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902871 | GCAACTAACCTGCAC[A/G]TTGTGCACATGTACC | 57626 |
rs190581414 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70069257 | GAAAGCCTTTGACAC[C/T]ATTTAAGTAGGTTCT | 57626 |
rs190582636 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734132 | ATGAATGGTTTAGCA[C/G/T]TATCCCTCTTGGTAC | 57626 |
rs190583321 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024397 | AGAGAGAGAGATTGA[A/G]GAAAAAACTCAGGGG | 57626 |
rs190584223 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866838 | GTAATAAGAGGGCTT[C/T]GTAATTCAGAACACC | 57626 |
rs190584684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853451 | ACTGTGAGTCGATTA[A/G]GCCTCTTTCCTTTAC | 57626 |
rs190584850 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809797 | CATCCTTCCACTGTC[C/T]TCCAGAGACCCATCT | 57626 |
rs190589065 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752808 | GGCTATATATGGCCA[A/T]AAGCGAATAGGTATT | 57626 |
rs190589094 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834577 | AATATATGTGAGACT[G/T]GTCCACTTTGGATAT | 57626 |
rs190590842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791509 | AACCAAAGACAGTGT[G/T]ATCACACTACATGAT | 57626 |
rs190591596 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70043175 | TCCGAAAATGCTGGG[A/G]TTACAGACATGAGCC | 57626 |
rs190592746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820098 | TGTATCTATTAAGTA[G/T]GATCTTGCAGGGCCC | 57626 |
rs190598343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061727 | CCACTCCAGGTTCTT[A/G]CATTTTCAAATTCCT | 57626 |
rs190601128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809627 | CATAGACCCTATAAA[G/T]CAACTACACAACTGA | 57626 |
rs190606100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912754 | CTGGGATTTTCTGTC[A/G]TCTAGCCTTTTCTTT | 57626 |
rs190614036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872974 | AAACTACAGTAGGAG[C/G]CATACACATCTTATT | 57626 |
rs190618080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890912 | ATATATACAAACATA[C/T]ACTTGTTTAATTAAT | 57626 |
rs190623567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843347 | GTAACAGAATAAAAA[A/T]GTGAATGCAAGAGTT | 57626 |
rs190628802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968078 | GTTGCAATGTATTTC[A/G]CTATCATCCTATTTT | 57626 |
rs190630023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929054 | TACTTAATGACAAGA[C/T]GGCACTTATCAACAT | 57626 |
rs190637528 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873767 | AAAGTATATATATTT[A/T]AAAAAGTAAATGAAG | 57626 |
rs190650845 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001730 | CTATCTTAAATAGAT[A/C]ATATTAGTGTATTTT | 57626 |
rs190672150 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69949056 | AGAAAATTGCAAAGC[C/T]AGTACAGCGATTTTC | 57626 |
rs190672706 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040530 | CTTGAAAACTATTGT[C/G]CTGCTTCCTTCTGAC | 57626 |
rs190675876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913471 | GGGTCTGGCGGTGCA[C/T]GCGATGGGGAGACAA | 57626 |
rs190678116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096902 | CCAACAGAAGGCTCC[A/T]AGAAAGAACATCAAG | 57626 |
rs190682909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101435 | GCCGTATATATATAT[A/C]ATTTTTTTTTAAGAC | 57626 |
rs190683826 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097941 | TGAAAAATATTGTCA[G/T]ATTATTAAATAATAT | 57626 |
rs190686876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074495 | CCACTGATTGATTAT[C/T]GTCCACCCAAGAGAT | 57626 |
rs190694002 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006800 | CTAGAAGAATAATAG[A/C]TTTCAAGCTCAAAAT | 57626 |
rs190703599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981839 | TTCTTCAAACCAAAA[G/T]AATGCAAATGTGACT | 57626 |
rs190709765 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045167 | ATCACCTGAAAAGTT[A/G]TATGGTTTTTCTAAG | 57626 |
rs190736444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712419 | ATATCCAAATCACCC[A/C]GCCACATTTGTCATA | 57626 |
rs190757355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750938 | GAACTGGGATGAGGT[C/T]CAGACACAGAGATGT | 57626 |
rs190787293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955512 | TTGTGCTTATCAGTT[C/G]TCTACAGGACCTGAC | 57626 |
rs190794898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757031 | ATTCAGTTAATTCTT[A/G]TCCTGCTTTGGTCAG | 57626 |
rs190796424 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789632 | CATTTTTTTTCCTCT[A/G]CTGTCCTACTATCTG | 57626 |
rs190797882 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974221 | TCCTACTTAAGAAAC[A/C]CATCAATGATTGATA | 57626 |
rs190801847 | snp | C/T | 0.00119808 | 0.024446 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726898 | TCATCATGACCAGTA[C/T]ATGTTTGTGAAATTT | 57626 |
rs190820801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989771 | TTGGCGTGGGTGTTG[C/T]TAGTGTATAGGAATG | 57626 |
rs190821191 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69718463 | CATGGATATGTAGCA[C/T]GAATGAGGAAAAAAA | 57626 |
rs190821340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813052 | TGGCACTATTCACAA[C/T]AGCAAAGACTCGGAA | 57626 |
rs190824117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825956 | TATTTGACGTTTATA[A/C]AACATATTATGGCCT | 57626 |
rs190827156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007659 | AGGTATCTATTTAAG[C/T]TTTGTTGGTGAACCA | 57626 |
rs190829385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737571 | CCAGCAAGACTGGGC[A/G]GTCTGGACTGGGAGC | 57626 |
rs190830831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029204 | GAGATCTTGAACTTG[C/T]GGCCTGTGATAGGTT | 57626 |
rs190831607 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795807 | TTACCCCATAGCAGG[A/G]AACAGATAAACCCTG | 57626 |
rs190835850 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757944 | CCTGAGTAACAAGAG[C/T]GAAACTCCATCTCAA | 57626 |
rs190838869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827420 | GTCAAGTATTTAGCA[A/G]GCCTTTTAAAAAAGT | 57626 |
rs190839150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046243 | AAATGTCATAAAGAG[C/G]AAGATGGGAAATATA | 57626 |
rs190841535 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780747 | ACATATATATATACA[C/T]ATATATATATACACA | 57626 |
rs190849533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066282 | TTAGTCTGTCTAAGT[A/C]ATCTAGCAATGAGAG | 57626 |
rs190854912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791335 | AGATTGGAAGATTTA[C/T]TTTTTTTTACGTGGC | 57626 |
rs190889260 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895485 | TTTTGTAATATAAAC[A/G]GGTTGATTTGTATAT | 57626 |
rs190892485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892532 | GATCTGTAAGAAGGT[A/G]TGTATATTGTGTCAG | 57626 |
rs190912976 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109910 | AATTAGTGCTTCATG[C/G]ATTATCTCACTTGAT | 57626 |
rs190922955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092825 | GAATATTTAAAATTA[A/G]ACAAATAGAGGAGTA | 57626 |
rs190927302 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989137 | GAAATGATTTTTGTA[A/T]ATAGTGTAAGGAAGG | 57626 |
rs190929329 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69969826 | ATATTTAGTTCTATT[A/C]ATGCTAGAGAACCTG | 57626 |
rs190931864 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930735 | TGATCACACAAGTGT[A/T]TAATACATGATCTGT | 57626 |
rs190935003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966488 | GAGCTCTGACAGAGA[A/T]GTACAAGGAGATTAA | 57626 |
rs190946344 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70101875 | AGTAAGCTTTCCCCA[A/T]ATAAGGTATTATTTT | 57626 |
rs190949174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028746 | GTTTGAGAGGCCGAA[A/G]CAGGTGAATTGCTTG | 57626 |
rs190955981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003062 | ACAATTAAAAGACTA[A/G]CAGAAAAGTGAACAA | 57626 |
rs190967544 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065690 | GTGCTTGGAGACAAC[A/G]AACTGTAAAGAGGAG | 57626 |
rs190992067 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033959 | CTTAAGCCCTAATAC[A/G]GACGAAATATAAAAT | 57626 |
rs191009145 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069963 | CACGAGGTCAGTAGA[A/T]CAACATCATCCTGGC | 57626 |
rs191009925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704051 | AAGGCTCCCTGATGT[C/T]CATTCAATACTCAGT | 57626 |
rs191022956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878193 | TAGCTACTCCTTGCT[A/G]TAAAAGTACTTACAG | 57626 |
rs191026992 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840092 | ACAAATGTTCATTGA[A/G]TGAATAAAAATGGCA | 57626 |
rs191030707 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860519 | GAATGTTTATAGATT[A/C]ATGAATCCAAAGTCT | 57626 |
rs191037438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708900 | CAATTTTTTTCACCC[A/G]TTCAATTTTTAACTC | 57626 |
rs191048504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713950 | AGCACAATGTTAGAA[A/G]AAAATCTCCTCAATA | 57626 |
rs191052235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936692 | AAAACACTCAATGTT[C/G]TAAGTTTAAAAGATA | 57626 |
rs191052418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896098 | CTTTTTCTTGGTGGC[C/T]GTTGCCTGGAGGTCA | 57626 |
rs191054148 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976514 | CTTTAATAAGTGCTA[C/T]ACTCCATCATAGGGA | 57626 |
rs191055311 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779327 | ATTCTGTTAAAAAAG[A/G]TCTTCCTTCCTTCCT | 57626 |
rs191058665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916869 | ATATTAAAAAACAAA[C/G]AATCTTATCAGAATA | 57626 |
rs191060391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993203 | TGAATGAGATATAGG[C/G]TTTATCAAGGGGAAC | 57626 |
rs191067002 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722341 | TTTCAAAAATTATAT[A/G]TAAATATATACCTAA | 57626 |
rs191068585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952590 | GCAGAGATGAAAACT[C/T]AAGTTCACAATCCAA | 57626 |
rs191080206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970514 | TGTTAGTACCTAAAG[C/T]ACCCAGATGCTCCTT | 57626 |
rs191116924 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69784376 | AATGCTCCAATTAAA[A/T]GACACAGACTAGCAA | 57626 |
rs191133142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877833 | TATCTGAAATCCATA[A/T]CCTCTGTTATATTTT | 57626 |
rs191138471 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854390 | TTTAACATCCAGCTC[C/T]CCCAGGAAAGCATAG | 57626 |
rs191145962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820931 | CTAAAACTCTGTTTT[A/C]TTGGAAAGGGCAATA | 57626 |
rs191162348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69891361 | TCTCAAAACTGTTTC[C/T]AGTATCAGAAATAAT | 57626 |
rs191164952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902528 | TGAAAGAGAGAATTC[C/T]GGATTAAGAAAATGT | 57626 |
rs191166593 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089886 | AATGGTGAGAGAGAA[A/G/T]TTGCTAATGCCTCCA | 57626 |
rs191171827 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916668 | GTCGGTGCAGCACAC[C/T]AGCATGGTACATGTA | 57626 |
rs191179023 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884450 | AAAAAAAAAAAACTA[C/T]GTGAAGCTAAAGATG | 57626 |
rs191185922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952241 | AGCAGAGTGCATAGC[C/T]CAGGAAAACACATGA | 57626 |
rs191197665 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69922074 | GCTGGGACTAAACGT[A/G]CACACGACAGTGCCT | 57626 |
rs191199621 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958380 | TGAGTTCAACATGGA[A/G]AGTGTTTCCCATATC | 57626 |
rs191200627 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985144 | AAACAACAACAACAA[A/C]AAAAAACCTCTGTGC | 57626 |
rs191201719 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083859 | TACCCCATACATGTA[C/T]ACAATTTTGATTTTT | 57626 |
rs191204666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942294 | TGAGCTTGGAAGGCA[A/G]GTTGCACTAAATTTG | 57626 |
rs191218729 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974859 | TTCTCTTGCAAATGG[A/T]AACTCAATTTTGTAG | 57626 |
rs191228649 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69956044 | TATATATTTATATAT[A/G]TTTGATATATATATT | 57626 |
rs191228899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991260 | CTAGAAAAACAAGAG[C/T]GAACCAACCCAAAGG | 57626 |
rs191237042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991090 | AAACAGAAATGAAGA[A/G]GTTATTTGAAAGTAA | 57626 |
rs191242397 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767008 | ACAATTTTGGTATAC[A/G]TTACCCATATCAAAG | 57626 |
rs191243927 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052292 | ACTAACCATGAAACA[C/T]CAAGATAAAACAATT | 57626 |
rs191252524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745446 | TTTTCCACTGTGAGG[C/T]TTGCATTTTCACTTT | 57626 |
rs191256189 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055516 | ATACACAGACAAATA[C/T]AAAATATTGTAACAC | 57626 |
rs191262915 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716192 | CTATAATTTCTCTAT[A/C]AATTCATTTGTCTGT | 57626 |
rs191264601 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029395 | TGAAGGTGAAGCCTG[A/T]TATTTGAAATTTCAG | 57626 |
rs191267161 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821359 | TCACTCTGTCGCCCA[A/G]GCTGGAGTGCAGTGG | 57626 |
rs191271040 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800841 | CCCTTAGAGAAAAAC[C/T]AATATTTATCATAAT | 57626 |
rs191298815 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69731414 | GAACAACCAACCATT[C/T]TTTATGCAAGCAGCC | 57626 |
rs191348381 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738352 | TTCTTCTCCAAATGA[A/C/T]AGCAACATGTCTCCA | 57626 |
rs191350520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800039 | CCAACCCCCACTCTC[C/T]GACCCCTGTCCATGG | 57626 |
rs191368394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765799 | CCCTCCGATCTGTTG[C/T]TAAACAGAGAAGGAA | 57626 |
rs191377671 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700163 | GTCTAATACATTTGA[C/T]CATGTGTTCATTTTG | 57626 |
rs191382209 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834998 | CATTTTAGAGATGTA[A/G]AAGTTATAACTGAAA | 57626 |
rs191382798 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805861 | CAAGGAATTTATAAA[A/T]TTATACTGGCATTTC | 57626 |
rs191393211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789431 | TTGAGTCGAGGAATC[C/T]GAGATTAAATCCAAA | 57626 |
rs191393490 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838786 | CACAAGAAATGAATA[A/C]GGAACTTAAAGATGA | 57626 |
rs191397946 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781041 | AGACCAGAAGTAGAA[A/T]CAGACTTCTTCTAAG | 57626 |
rs191398444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021348 | CTTGATAGGCCACTT[A/C]TTTATAACACTGAAT | 57626 |
rs191403162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802724 | TCACGACCCTCTCAC[A/G]TGCACCCCCATAGAG | 57626 |
rs191403811 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772928 | GTTTTTTTTAACAAC[A/G]TTGATCCAAACAGGT | 57626 |
rs191405311 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039732 | GCAACCTCTGCCTCC[C/T]GGACTCAAGAGATTC | 57626 |
rs191410586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103566 | GGTTGCAAAACTAGA[A/G]TTGAAAGAAGATCGT | 57626 |
rs191415553 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70059405 | AAACTCCTGACCTCA[A/G]GTGATCCACCTGCCT | 57626 |
rs191418547 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086073 | ATGCCATATTACTAT[C/T]CCCATCTTATCTAAT | 57626 |
rs191421144 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873487 | TTAAGTTTGCCTTCC[C/T]TTTGTCCATTCAATA | 57626 |
rs191424862 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841148 | CAAATAAAAAATAAA[A/T]ATCTTTAAACTTTTT | 57626 |
rs191425737 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877656 | CAGTTATCTATCACT[A/G]TCATTTTCCCTTTTT | 57626 |
rs191426159 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70074451 | GGTACTCCCCACCCC[A/C]ACATCTACCTCATCT | 57626 |
rs191428397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825209 | TACATAATTGAATTG[A/G]TCAGGCTACTGAGAA | 57626 |
rs191442570 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098769 | TTTTACTATCATAGG[A/G]TATCTTAATGTTCCT | 57626 |
rs191444066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879556 | ATGGACAAACCTTAC[A/G]TTAATGAATCCAAGA | 57626 |
rs191448785 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941883 | ATGAATAAATCCCTG[A/G]AAATATACAATCCCC | 57626 |
rs191456195 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944650 | TTCACACCAAATTAA[G/T]CTATAGATGTACTAC | 57626 |
rs191478118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974466 | TAGAATATTATGAAT[A/G]TAGAATAATTGCTCA | 57626 |
rs191478180 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70037801 | TTCTAACTTCAATTA[C/T]TTTCTTCACTTCTTA | 57626 |
rs191482290 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70007802 | AAACACAGAGGTCTC[C/T]GTACCCACATGTTTC | 57626 |
rs191489181 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976908 | CTGCGTATTCTTTCC[C/T]TCTCAAGGTATTTAC | 57626 |
rs191493329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092449 | TATATTAAACTCTGT[C/T]GTCTTTGCTTAGGTA | 57626 |
rs191501293 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072453 | GTCATGAGGTCAGTA[G/T]CCCAGTAAAACCAAA | 57626 |
rs191502621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012907 | GATTCTGTATAAAAA[A/T]AATAATAATAATAAA | 57626 |
rs191505811 | snp | A/G | 0.00676609 | 0.0577691 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700449 | TTAAAATTACATTTG[A/G]TGTCAGCATAGTATT | 57626 |
rs191520097 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738992 | AAACAATGCAAAGGG[A/C]AGCCAGAGAGAAAGG | 57626 |
rs191520215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051823 | CTTTTCAGAGATTGA[C/T]GGTAGACTGCTAAGG | 57626 |
rs191551858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077807 | TTAGAAACATATTAT[A/G]TACACAAAAAGTTAA | 57626 |
rs191575287 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719160 | AAGCAAGGAATAAAA[A/G]AATAAGAAAATAAAA | 57626 |
rs191586316 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69722703 | TACATTGTTTATGGC[A/T]ATGTAAATTAGGAAA | 57626 |
rs191593276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706344 | GAGGAGAAGAAATTC[A/G]TAATGCAGATACCTT | 57626 |
rs191596959 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759332 | GAACAAATCAAGCAG[G/T]TATCAAAAATATTAC | 57626 |
rs191605149 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786874 | AATAACAGACAAACA[A/G]AGCCGAATCATGAGG | 57626 |
rs191629192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978977 | AGACCCTGGTTTGGG[A/G]GGCTGGGGGTCATAG | 57626 |
rs191634352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767518 | CCTGGGTAACATACC[A/G]AGAACCTGTTCCTAC | 57626 |
rs191634554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809910 | ACTATTCGTTTATCA[A/G]ATAAAATAGAGTTTA | 57626 |
rs191639077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791988 | AAAATTGCAGAGCGT[C/T]AGGAGAAATAGCGAA | 57626 |
rs191639952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043505 | CCTTCACATTCGCTC[A/G]CTACTTACTCATTGA | 57626 |
rs191642408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799394 | AAAAAGGAAAAGTCA[A/G]GAATTGATTTGGATT | 57626 |
rs191643167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995219 | ACACTATTATTTACT[A/C]TCTGGTATTTTACCC | 57626 |
rs191646285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016662 | AGCACAGGCCTGCAG[C/G]TGCCCCTCCGCACAA | 57626 |
rs191647781 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062144 | CTGATTCCAGCTACT[A/G]CAATACAATGGGAAG | 57626 |
rs191649298 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035480 | AAGGATGGTTAATGG[G/T]TACAAAAAATAAATA | 57626 |
rs191654141 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70078039 | GTTCTCTACAGGTGC[C/T]TCTCTAAATGATCTT | 57626 |
rs191654637 | snp | A/G/T | 0.00319074 | 0.0398324 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724220 | TTCCAGATTGAACCA[A/G/T]TGTAAATTTTGCATG | 57626 |
rs191658861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844982 | TTTGCTCCCGCAGGA[C/T]GAGACATCTGTGAAC | 57626 |
rs191660546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765299 | TAGTTCATTAATACA[C/T]TTATATACTTTATGA | 57626 |
rs191661340 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865991 | AAATCTAATGGTCAG[A/G]ATAAAAATTCCATCT | 57626 |
rs191664401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895146 | ATATAATGAATTCTT[C/T]CTCCATGAGAAGGTA | 57626 |
rs191666231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746546 | CTATTTATACTCAAT[A/G]TAATAACTGATTTTA | 57626 |
rs191673813 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785617 | AAAAGCAAGAGCAAA[C/T]GCATTCAAAAGCTAA | 57626 |
rs191673952 | snp | C/G | 0.000400853 | 0.0141515 | synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107613 | CCCCGCCGGGCCGCC[C/G]GTGGAAGGAGACGGG | 57626 |
rs191675129 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858015 | ATAACTGGTTTTCAA[C/G]TGACTACACCAGTTG | 57626 |
rs191684979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902345 | GGAACATTTTAAGTA[A/G]AGGTTAATTAACAAA | 57626 |
rs191685156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090079 | AACTCTGTTTTTATA[C/T]GGGAAATGAATTGTG | 57626 |
rs191692993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865610 | CATGGAGTCCGTTGC[A/G]TAAAAATGATAAGGC | 57626 |
rs191701858 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883882 | GCTCCACCTCTCCCC[A/T]TGTCTCCTGGGACAG | 57626 |
rs191708932 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827626 | TCCCAGCTACTCGGG[A/G]GGCTGAGGTAGGGGA | 57626 |
rs191720265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923689 | TAGTGAGAGACAATA[C/T]AGTACTGATGAATAT | 57626 |
rs191738045 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901690 | TTTGCAATGTGGTTG[A/C]AAAATAAATTGATGA | 57626 |
rs191739720 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109574 | ATTAAGTGCACAAAA[G/T]ACCTATTTTTAGGGG | 57626 |
rs191741542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993984 | TGGGTCATTAACTAG[A/G]TGTTTAAAAAATGCT | 57626 |
rs191742201 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105667 | TTATATTTACTCAAC[A/T]AAAGGGTATAAAAAT | 57626 |
rs191764007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033269 | CTGTTAGGCTTCTAA[C/T]AATTTTTTGTTTTGT | 57626 |
rs191815863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932960 | AGAGTTCTCCATCTA[A/G]TTCAGGGACAAAGAA | 57626 |
rs191824913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073328 | AAACCAAACACCACA[C/T]GTTCTCACTCATAGG | 57626 |
rs191827239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949472 | AACATTATCAACGTG[A/T]CTTATCACTGGTGAT | 57626 |
rs191838874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982791 | GAAGAAAATACAAAG[A/C]GGGTCATTATATGAT | 57626 |
rs191843700 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967379 | TAAGACATCAGTGGA[A/G]GAAGTAACCTTACTA | 57626 |
rs191850971 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000417 | ACAAAGTTTCTTCCC[A/C]AAACTAATAAAACAA | 57626 |
rs191852564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020570 | CTCTTATCATTGGCC[A/C]ACTGGGCTGTCTTCC | 57626 |
rs191858561 | snp | A/C/T | 0.00239401 | 0.0345304 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710916 | TCAGAGTGTGAGCTC[A/C/T]GTATCAGAGACTCTA | 57626 |
rs191864827 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038691 | TGCCTCCCGGGTACA[A/G]GTGAGTCTCCTGCCT | 57626 |
rs191879495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772841 | AATTAAACATTAATA[A/C]ACATCAATATGAGAT | 57626 |
rs191887882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744153 | AATGTAACAGAGAAC[A/G]TAATCTAGCTTTAAG | 57626 |
rs191919853 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749400 | TCTGATAATTTTTAA[A/C]ATGTCTTTTAGATGT | 57626 |
rs191921645 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704646 | TAATTAATCATGCTA[A/T]TTTAAACATTTGGTA | 57626 |
rs191926247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789091 | TACATATCCATCTGT[A/C]TATACCTATGCCTAT | 57626 |
rs191928065 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70103658 | TCTAAGCAAAAGCAG[C/T]AATTCTTGAAAGAAT | 57626 |
rs191934877 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824721 | AGGTTGAAAAAATAT[A/T]CAAAGGAATAGTTGT | 57626 |
rs191939177 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086768 | GGCAGGCAAACTACA[A/G]TGTGATGAGTAGTAT | 57626 |
rs191943798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788599 | CACACCAACATGGCA[C/T]ATGTATGCATATGTA | 57626 |
rs191944923 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783967 | CAAAGGGAAGCCCAT[C/G]AGACTAACAGCTGAT | 57626 |
rs191957962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923375 | TCAAGTATGTCTCCG[C/T]TGGAGTTGCTTAGAG | 57626 |
rs191959487 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887348 | GTTTCCTCAGAGGGC[A/G]CAGGTAAACCTTGAC | 57626 |
rs191983057 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960733 | TCAACAAATGTTTGC[C/T]ATAATGGCAAAATTA | 57626 |
rs191997756 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985647 | GGTATATGCCCAAAG[A/G]AAATGAGATGAATAT | 57626 |
rs192002712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844360 | TTATGAATAAAATAT[C/T]GTGTAAAATGTAACT | 57626 |
rs192014110 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921040 | AGAGCCTCTGTATGT[A/T]AAAATGTAAATGTTG | 57626 |
rs192014621 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817243 | GCTTTCGTTGAAAAT[G/T]TAGACACTGGAATGA | 57626 |
rs192019995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023506 | TAAGTTCATACTCAC[A/G]TTTTTCTAACTGCCA | 57626 |
rs192020785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883013 | GCTATTATCTCTTAT[C/G]ATTCCCTCCTCTCAT | 57626 |
rs192031032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061492 | AAGTGTGGGCAGCAT[A/T]TTGTGCTCACTCTCT | 57626 |
rs192031755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948270 | AGACAGGAAAGCACG[C/T]AGCAGAAGAGTAACT | 57626 |
rs192036910 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871408 | GTTAGCACCTGGATC[C/T]CCTTTAGTCACGCTA | 57626 |
rs192043416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889131 | CATCTCCCTTCAAGT[A/G]TCAAGAGTTTTTAGT | 57626 |
rs192050632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088351 | GAGAGCTTTGATAAT[A/G]GATGATAATTCATTT | 57626 |
rs192054971 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850810 | AGGCTCATTTGTCAC[A/T]GTGCCTCCAGATCAA | 57626 |
rs192056801 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953216 | AACATTTTAAATAGT[A/G]CTAAGAAGCATCAAT | 57626 |
rs192077923 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910140 | TCACGAATTCCTTAT[C/G]TTTGCACAACACTTG | 57626 |
rs192079996 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69927688 | TAGGAAAATCACAAA[C/T]AAAAACCACGAAATA | 57626 |
rs192081757 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971173 | TTTTTCCATGCCTCC[A/G]TTTTCTATATTATAG | 57626 |
rs192088507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733123 | TTTAGAATAACTGAT[A/G]AATGACTGTTCTGAT | 57626 |
rs192091300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69986087 | CAAGTACTGAAGGAC[C/T]AATATTACTATGTTC | 57626 |
rs192093260 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946570 | TGGGCTGAAGGGCAG[G/T]GGCATGATCCTAGCT | 57626 |
rs192115192 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057842 | AAGAAAAGGCCAATA[A/T]CTCTGATGAATATTG | 57626 |
rs192115849 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69775844 | AATTTTAGGTGGTAA[C/T]TGCATTTTAAAAAAA | 57626 |
rs192174719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777633 | TTTCACTTTTTTGGC[C/T]GAAATGTAATTTTTC | 57626 |
rs192176176 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69735119 | ATGCAAATTACCACA[C/T]AAACAGATCAAATAA | 57626 |
rs192189833 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100170 | TCTTCTGATCTATGA[A/C]TATTATATATTCATA | 57626 |
rs192192635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845618 | TCTATATACCTGACA[A/G]AATTTCAAGTACATT | 57626 |
rs192197396 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810387 | TAAACACTGGGAAAG[C/T]TCTCAAACCATACGA | 57626 |
rs192217372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771170 | ACTGCTATCTTCACC[G/T]TAATCTGAGTTTACT | 57626 |
rs192245874 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949640 | CTCTATCTCCATGAC[A/G]GTGGAATAACTGGCA | 57626 |
rs192251275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869682 | TCAGAGTGTTTAAAA[C/T]AATAAACTATATTTT | 57626 |
rs192258337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803880 | TTGTCAACAATCAAA[A/G]TAAATTTGGAAAAGT | 57626 |
rs192262505 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831798 | GATGTTTTCAAATAT[G/T]CAAGTCAATAGATGT | 57626 |
rs192263801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008497 | GCGTCATTGGCTATG[A/C]ACCCAAATATGCATG | 57626 |
rs192266452 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907407 | TTTATTTACATGATA[C/G]TTGTGTGCTTAGAGA | 57626 |
rs192275899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983820 | ATATTAACCAAAATA[A/G]CATGGCACAGGCATA | 57626 |
rs192279318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047893 | CAGTCTTGGTGCTTT[C/T]AGGTGCTCAGTTTTA | 57626 |
rs192286341 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874495 | CAAAATCTTAAAATC[A/G]CTGGAAAAGGTCTAA | 57626 |
rs192290909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829491 | CTATCCAAATAAGAA[A/G]GAACCAGAAAAACAA | 57626 |
rs192296499 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811024 | CAGATGGATTCACAG[C/T]AGAATTCTATCAGAC | 57626 |
rs192296519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099401 | CACAGTGAAGCCTTC[C/T]GTGCAGAGATGCTTA | 57626 |
rs192300696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837498 | ACCTATACTTAGGTA[C/T]CTAGCTATATAATGT | 57626 |
rs192301716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943882 | TGAGAGAAAATCAGA[C/T]GGAAGACCTACATGC | 57626 |
rs192303706 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855531 | GGGAGAGGAAAGAGA[A/C]CACGTGGAAATAATG | 57626 |
rs192305091 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975123 | ATGGCTTTAAAAATA[A/G]TATCAGTATGACACA | 57626 |
rs192310478 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69991580 | CTAGAAAAGGTAGAA[A/G]AAATGGATAAATTCC | 57626 |
rs192318233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892720 | TCGGGAAAGCCTGTT[A/G]TATGCATAATCAGAA | 57626 |
rs192321359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931424 | AATTAACTTTGTCTT[G/T]CATAAAACATGACTG | 57626 |
rs192324902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914767 | CATGAAAACAATCTA[C/T]AATCCTTTCCTAGAA | 57626 |
rs192328220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009609 | TTGGAAAAGAAGTAT[C/G]GACGTTGAAATATTG | 57626 |
rs192336263 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949246 | TTCTGTTCCAGGATC[A/G]CATTCAGAATAGTAC | 57626 |
rs192344011 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048243 | CCTGAACGTGGTTCT[A/G]TGTGATTATCCATCT | 57626 |
rs192347106 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70003234 | ATCAAATCATATTCA[A/T]GCTTTTCCTTGAAAC | 57626 |
rs192352164 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068267 | AATGGCGTGAACCCG[A/G]GAGGCGGAGCTTGCA | 57626 |
rs192370726 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042141 | TCCATAATGTAGTTT[G/T]GGATATATAAGGAAA | 57626 |
rs192381878 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729238 | CATATATACCCCTTA[G/T]CTTAATCTGTCTTAC | 57626 |
rs192389476 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70077437 | TTAAAAAAAAATTAG[A/T]CGTTGAAGAGTTTGG | 57626 |
rs192398636 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797477 | TGTAAGATATATAAG[A/C/T]AAATATTTGCTATGC | 57626 |
rs192426115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833211 | CAAACTATGCATCTG[A/G]TAAAGGACAAATGTC | 57626 |
rs192450692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720175 | TGATTGAAAATTGCT[C/G]AAGTTTACTTGATAC | 57626 |
rs192461225 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741234 | CTCATTGCTTTTCTA[A/G]TAAACTCACATCTTC | 57626 |
rs192461582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870922 | GGATTGAAACTGACT[C/G]CTTGCAACTCTTCCA | 57626 |
rs192469654 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752434 | AAATATATTTTGTTA[A/T]TTATATTAATATGTA | 57626 |
rs192474283 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896893 | GGCCAGGCTGGTCTC[A/G]ACTCCTGACCTCATG | 57626 |
rs192487127 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782348 | GCACCGTGTGCTAGC[C/T]GAAGCAGGGCAAGGC | 57626 |
rs192493870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761125 | AGACAAATTAAATTT[A/G]AAAATGTTTAATTGA | 57626 |
rs192504398 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714605 | TTTATTTATTTATAT[A/G]TTTTTTGAGACAGGG | 57626 |
rs192506163 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937769 | GCTGAAGCCAAATAC[A/G]TAAGTGAAATTTCCA | 57626 |
rs192507792 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833734 | CAATCAATGAGTGGA[A/T]AAAGAAATAATGGTA | 57626 |
rs192509309 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816388 | GCCTCAGCTTCCTGA[C/G]TAGCTGAGATTACAG | 57626 |
rs192514000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754283 | ATTCTCAAAAATATA[C/T]TATCACATATTGATG | 57626 |
rs192514148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094691 | GATTACGGAACTTCA[A/G]TGCTTTTGTGGCAAT | 57626 |
rs192515321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971709 | GAACCATATATTCTA[C/T]CTTGCAGTTATTTGC | 57626 |
rs192516027 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69797816 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTAAAA | 57626 |
rs192526250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897628 | CCAGAGTGCGTTGAC[A/T]ACCTAAAGAGGAGGG | 57626 |
rs192538461 | snp | A/C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69862699 | ATACTAAATGAGGTA[A/C/T]TAATGCAATAAGACT | 57626 |
rs192539700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004753 | ACACCCAAATAACTT[G/T]ATTATATGAAATTGA | 57626 |
rs192542163 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880294 | ACATAATTCATTAAC[A/G/T]TTAGTTGTAGAAGTG | 57626 |
rs192554044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939270 | CAAATTTAAACTGTA[C/T]AATTGAAATGGCTTT | 57626 |
rs192555586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792820 | TTTTTACATGAAATA[C/T]TCAGAATGAGCAAAT | 57626 |
rs192565590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918003 | AATTGATATTGATAT[A/G]TTGTAAGGCACCCCA | 57626 |
rs192567819 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994453 | GCAGATACTTTGCAA[A/C/T]ATGATGCCTATTTTT | 57626 |
rs192567997 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954361 | TGATTAAAGTAGGAA[A/C]ATACATAGCAGGTAC | 57626 |
rs192577990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014725 | AATGTAGTATATGAA[C/T]GATGAGATAATGTTA | 57626 |
rs192584221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988313 | TCTTTTTCATGGTTG[C/T]ATACTATTAAATGGT | 57626 |
rs192586816 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972014 | TTTTTTCTGAAGTTG[A/C]TACAGAGATATTTTA | 57626 |
rs192587193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071022 | AACAAGGGAAATATG[C/T]AGAATACAGTTACAA | 57626 |
rs192593610 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828626 | GCCTAAAAACCTTGC[A/T]TACTTTCTCAGCAGG | 57626 |
rs192597887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034735 | AGGAAATTATACACC[A/G]TCGTTCTTTTCTCCA | 57626 |
rs192605610 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053133 | ATGGTGAAATTTAAG[G/T]GTAGTCTTAAAAGAA | 57626 |
rs192612496 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070458 | GTGGAGTAAAATATT[C/T]AAAATGTTAAAAGAC | 57626 |
rs192623569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866637 | GAGATGTTATGGAGA[A/C]AATCTTCACTGTAAA | 57626 |
rs192625088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715636 | GTGAAAATGGACTAA[C/T]ATAATCCTCATATTA | 57626 |
rs192643586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753507 | TGAATGAATGAAGAT[A/G]ACAAAAATAATACAG | 57626 |
rs192663423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933835 | AAAAATCACAAAGTT[A/C]TTTGGTCTTATTTCT | 57626 |
rs192664665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723377 | TGATTAATATACTAA[C/T]TACCTAATTTGTTCA | 57626 |
rs192666748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967614 | ACAACCTGGTGGGGC[A/G]TTGTGGCTCACGCCT | 57626 |
rs192688730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822803 | ATAGAATAACTGGTT[C/T]AATATAATTATCTGA | 57626 |
rs192694312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001704 | CTATCTATCATCTTT[A/C]TACTATCTTCCTATC | 57626 |
rs192702105 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067853 | AATAATATGACAACC[A/C]GTGGAGCAAAATTTT | 57626 |
rs192709333 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69856220 | TTTAAAAAAATCTTC[A/C]TTCATTTCAAAGGGC | 57626 |
rs192713066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921559 | AAACGTGGCCATACC[A/T]ACGCATTGTGAAGAC | 57626 |
rs192730008 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893645 | ATTGTTATGTATGAT[A/G]CTCTAAATACGAAAG | 57626 |
rs192742771 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711966 | GCATTTCCCTGACGA[C/G]TAATGCCATCCAATC | 57626 |
rs192749891 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750499 | GTGAGATATTAAATA[C/T]ACATGTATGTGTGTA | 57626 |
rs192759922 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058767 | AAGTCATCCTAGGCA[A/T]AAAGAACAAAACTGG | 57626 |
rs192759954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781604 | TGTTGTTCTCATTAG[C/T]TTAGGTTTTGTTTTC | 57626 |
rs192761685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030869 | AATAAAGAAGAAAAG[A/G]GAGAAGAATCAAATA | 57626 |
rs192770952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068403 | AAAATTATATTTACA[A/G]TGACACTGATTAATG | 57626 |
rs192777627 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815480 | ATACCACATGTTCTC[C/G]CTTATATGTGGGAGG | 57626 |
rs192795000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917426 | CTTTTTAAACTGCCT[A/G]TAAAACTGACCTAGA | 57626 |
rs192805853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741537 | ATAATCAGAGTACCA[A/T]CAATTTTTGTTTCTG | 57626 |
rs192814326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953614 | ATTAAGATAAAATAT[G/T]ATAAAATCATGAATA | 57626 |
rs192815401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988005 | TGTTCAGGCTTGTTA[C/T]AGAGGCGAACTCATG | 57626 |
rs192818770 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782679 | AGCTCAAACTGGGTG[C/G]AGCCCACCACAGCTC | 57626 |
rs192820072 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804899 | TTTAAAATCAAAAAA[A/C/T]TTTTTATGATCCATA | 57626 |
rs192825375 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024879 | CTTCCTGTGCCTCTA[A/T]GGATATGCAGACACC | 57626 |
rs192833264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878856 | GGAACCAACCCAGAT[A/G]TCCAACAATGATAGA | 57626 |
rs192839503 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093741 | TTTTGAACCAACTAC[A/G]TCATATGTAAAGACC | 57626 |
rs192840522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840829 | TATTTCTAACAAGGG[C/T]CCAGTGGTGTTCATA | 57626 |
rs192844102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917261 | TTTAAGTAAATAAAA[G/T]GAAATGCTTAAAACC | 57626 |
rs192868907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734791 | AGAATATCAGTAAAA[C/T]AGAATATTAAAGGTA | 57626 |
rs192877462 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978313 | TCCAAAAGGAAACCC[G/T]GATGCTTCTTCTGCT | 57626 |
rs192882621 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015342 | TAAAGGTAAGTATTT[A/G]TGTATCTAAACATAA | 57626 |
rs192891771 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054008 | CTTTGATGGCATTTT[A/G]TTCCTCTCATTTCTG | 57626 |
rs192899267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777251 | TATTAAACCTCTTTT[A/T]CTTTTTAAATTATCC | 57626 |
rs192902866 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100400 | GCTAAGCTTGCTACA[G/T]TTTTTTGTCGATTTC | 57626 |
rs192908061 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801670 | TAGAAAATCTGAAAT[A/T]CTAGATAGAAATTTT | 57626 |
rs192916034 | snp | A/C/T | 0.00239401 | 0.0345304 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875703 | ATTTTGTAACTTGAA[A/C/T]GGTGAATGTCACAGG | 57626 |
rs192924382 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837624 | TCTCTCTCTATATAT[A/G]TGTGTGTATATATAT | 57626 |
rs192926169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915062 | CATTGGAATGCAAAA[A/G]TGGTATAACACTGCT | 57626 |
rs192945179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767087 | ACGAAAAAGATACTA[A/G]GTGTAGATATATCCT | 57626 |
rs192952443 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723989 | ACTACAGGTGCCCAC[C/G]ACCACGCCTGGATAA | 57626 |
rs192959597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801199 | CACTTTTGTTAACTG[A/T]AGAATGACCACTCTA | 57626 |
rs192961688 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107946 | GACACCACCAGGCAG[C/G]AGCAGAGGCAGGACT | 57626 |
rs192971222 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074133 | TGCCCGGCACCTTAA[A/G]CCTCCGCACCCGGCC | 57626 |
rs192976152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70049981 | ATCAGACTAATAGAT[A/G]ATTTATATAGAAAAA | 57626 |
rs192989310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867198 | ACATAGTTTTCTTAT[A/G]TTATAAAGTATTTTA | 57626 |
rs192992052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967095 | AGGTTTTTTGATATA[C/T]TGATTTTGTTTCCTT | 57626 |
rs192996380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903388 | CATCTGCCCCAGCCA[A/G]TCAGAACTCAGCTGT | 57626 |
rs192999332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942975 | TCTAGAACTGTTCCT[C/T]TGCCATTTTTTCATC | 57626 |
rs193003338 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998382 | GGAGCACAATTATAC[A/T]TCAACTTCCAATAAA | 57626 |
rs193013822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038429 | TGTCCTGGAGGGCAA[C/T]TGCTGGGTCATGTGC | 57626 |
rs193026648 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824899 | CATCTCAATGAATGT[A/G]AATTTTGCCTAAAAT | 57626 |
rs193029198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762255 | GAATTAACTGAATTT[G/T]CTTGGTCAAAGGTAT | 57626 |
rs193036941 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861059 | TTCTAATCATCAGTA[A/G]AATAAAGTATGTTTT | 57626 |
rs193056792 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749138 | CTTGCAGAATGGGCT[A/C]ATTAGGTAGGGTGAA | 57626 |
rs193056996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896555 | GGATGACCCTCAGTC[A/G]TTCAATAAAATGTTT | 57626 |
rs193066033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936975 | CCCGTGGAGAATAAT[A/G]GCTGCTGCTTCTCTT | 57626 |
rs193070919 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709819 | TCGTTGTTGAAGCAG[A/G]GTAATGATTATAGGG | 57626 |
rs193072338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964534 | ATGGATCCTTTTAAA[C/T]CAAATTTTGAAAATT | 57626 |
rs193087980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995020 | AAGACAGTGTGGACA[C/T]GAGTGTCACTATAGA | 57626 |
rs193099661 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888464 | GTGGTCTTTCTAAGA[A/G/T]AAATTTTGAGATACA | 57626 |
rs193101742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085948 | GTATATGGTGACAGA[C/T]ATTTCATATTGCTAA | 57626 |
rs193101987 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69850081 | TAGCAAAAATCCATT[A/G]CAGAAATAATTTGGG | 57626 |
rs193103902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926450 | TCTATAAAATAAGAA[C/T]CTCGATTTCCTCATA | 57626 |
rs193113200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964086 | TCTTGCTTTGTCACC[C/T]AGGCTGGAGTCCAGT | 57626 |
rs193124862 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026542 | TGTCACTAGTTTACT[C/T]TGCTACTGAATAAAT | 57626 |
rs193130392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063023 | TTCACATCATAGCTG[C/T]CTCCATGAAATACCT | 57626 |
rs193146314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070598 | GTAGGTCTACCTCAT[A/C]AGAATGTTAAAGAAG | 57626 |
rs193169017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746189 | AATATTTATAAATAA[C/T]TGTCATAATAATCCA | 57626 |
rs193174068 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69785172 | GCTGGGATTACAGGC[G/T]TGAGCCACCGCGCCC | 57626 |
rs193177427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705767 | GCTGTTTGTAAAATA[C/T]TATATGATCCAAAAA | 57626 |
rs193182390 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821982 | AGGCAGGCAAATCAC[A/G]AAGTCAGGAGTTTGA | 57626 |
rs193185906 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091439 | CATGTGTTGTTCTCT[C/T]AGCAAATAGTCATCT | 57626 |
rs193187584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845657 | ACACAAAAAATGAGA[C/T]ACTGTATTTCTATAA | 57626 |
rs193201189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982166 | TAAAAATAAAAAGTG[G/T]CTCATGCCTGTAATC | 57626 |
rs193203376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922200 | GATTCTCCTGCCTTG[A/G]CCTGCCAATGTGCTC | 57626 |
rs193206115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019694 | AAGTTACACAGTTTA[C/T]AAATGATAGTGGTGT | 57626 |
rs193206942 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959248 | TTTTGACCTAGTTTT[A/G]CACACAGGAAATGCA | 57626 |
rs193231381 | snp | A/T | 0.00676609 | 0.0577691 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701023 | TAGTGAAAACAATCC[A/T]TTGTGTTTGCCAGTT | 57626 |
rs193240595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727407 | TGAATAGTGGACAGT[A/C]ACAAGTTAATAAGAA | 57626 |
rs193255204 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102832 | CAAAAAGCAAGTTTT[A/T]AATCAATGCCACTAA | 57626 |
rs193258178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871160 | AACAAGATATGGAAG[C/T]TGCAAAGGCTTACCA | 57626 |
rs193263314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909457 | AAAGAAAAGAAAGCC[C/T]ATTAAATCTAAATTA | 57626 |
rs193263554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945679 | AATATTATCAGTGCT[G/T]CAGAAAATGCACATT | 57626 |
rs193270968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978016 | CTCCTTTAAATATTT[A/G]AAATTAATACAAATT | 57626 |
rs193277652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005302 | TTACCAAATTAAATT[G/T]ATTAAGATTAATATA | 57626 |
rs193281969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043759 | GAGGCTGTACCATCT[C/T]AGTTTATATAATTAT | 57626 |
rs193285750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079005 | GCAGTTTTATTGCTA[C/G]CAGAGAAATGGAATA | 57626 |
rs199500873 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833034 | AATTCTTCTGAACAT[G/T]GTCTTAGGCAAAGAC | 57626 |
rs199525417 | in-del | -/AAAC | 0.0777841 | 0.181223 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736196 | AAATTAGCAAGAAAG[-/AAAC]AAACAATCCCATTAA | 57626 |
rs199547653 | in-del | -/TC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69851138 | TTTTATAGGTAGCTG[-/TC]TCTTTTTTAAGTACT | 57626 |
rs199548882 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69849737 | AAATCAGAAAAAAAA[A/T]TCTGCTATTTATTGT | 57626 |
rs199557486 | in-del | -/ATAAAA/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69943670 | TGTGTATCTGCTGTT[-/ATAAAA/TA]ATAAAAATAAAGTTA | 57626 |
rs199562330 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69845891 | AGATGTCGATATTTG[-/A]AAAAAAAATAGATCT | 57626 |
rs199565023 | in-del | -/A | 0.0944967 | 0.195752 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949766 | TTGAATAAATGTTTC[-/A]AAAAAAGGAAGGAGA | 57626 |
rs199565568 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961214 | AGATACAGAATACAG[-/A]ATTTTTTTTAAAAAA | 57626 |
rs199567166 | in-del | -/ATAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833811 | GTTCTATATATATAT[-/ATAC]ACACACACACATGTA | 57626 |
rs199574323 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69774673 | CTTAATAAAAAAAAA[A/C]ACACACACACAAGCA | 57626 |
rs199580188 | in-del | -/TGT | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942365 | TAACTCTAATTATGC[-/TGT]TATTTAATTGAAATT | 57626 |
rs199587951 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69753839 | ATGGCATAGAAATAA[A/T]TGAAAAAAAAAATTT | 57626 |
rs199589515 | in-del | -/AC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69775712 | TTTTTTGTTTTTGAT[-/AC]AGTGTCGTGCTCTGT | 57626 |
rs199595229 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69812047 | GGGCGTTTAGTGCTA[C/T]AAATTTCCCTCTACA | 57626 |
rs199599605 | snp | A/G | 1.65499e-05 | 0.00287657 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69707655 | AGTTTGTGGGTCATA[A/G]GATTCCATAGTGTTG | 57626 |
rs199609578 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69748072 | CAATAGAGCCTATAT[C/T]CTAGAGGAGAATACA | 57626 |
rs199618546 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902954 | CTTTTCCATTATATA[-/T]TATAATGAAAAAGTA | 57626 |
rs199624721 | in-del | -/T | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989264 | TGTCAAAAATCATGG[-/T]TGTAGGTATGTGGCT | 57626 |
rs199626224 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780745 | ATACATATATATATA[C/T]ATATATATATATACA | 57626 |
rs199630248 | in-del | -/TTTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69997275 | ATTCAAATTTTATTT[-/TTTC]TTTTTTATTTTTAAT | 57626 |
rs199630475 | in-del | -/ATG | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962694 | AGAATGAAAAAAATT[-/ATG]ATATTTTCAAGTATA | 57626 |
rs199632877 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890669 | ACACACACACACAGA[A/G]ATATGTATCTCCTTG | 57626 |
rs199637580 | in-del | -/TA | 0.100231 | 0.200173 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840685 | TTTGAACATTAACTT[-/TA]TATATATATATATAT | 57626 |
rs199642956 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70010911 | AAAAAATAATAATAA[A/T]AATAAAATAAAATAA | 57626 |
rs199651149 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69796856 | TCCAATTACAAAGAG[C/T]TTGTCATCAATAACA | 57626 |
rs199657006 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69816367 | CCAGGCTCAAGTGAT[C/T]CTTCTGCCTCAGCTT | 57626 |
rs199659111 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961827 | TGAGATTTCTATTAT[G/T]TTTTATTTGCCTGTT | 57626 |
rs199659260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995065 | CCAGTTAAGCCAGTC[A/G]CCTTTTAAGGATAAA | 57626 |
rs199670135 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69762769 | CCTCAATTTTTTCTT[-/A]TGTCTCTATGAACAA | 57626 |
rs199672505 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69915537 | GGAAAACCGGCTAGC[A/C]ATATGTAGAAAGCTG | 57626 |
rs199678351 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964963 | CTATACTACCCCCAC[-/A]AAAAAAAAATACAGG | 57626 |
rs199679340 | in-del | -/AGA | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920777 | CTTAAGAAAAATAAG[-/AGA]AGGTCAGCAAAAATA | 57626 |
rs199685444 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69742986 | TTAACTAGATGGAGA[C/T]TAAAGTGAAAACATC | 57626 |
rs199696586 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69753832 | TTCCATAATGGCATA[A/C]AAATAATTGAAAAAA | 57626 |
rs199698993 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69784208 | ATGGAAAGGAAAAAC[C/T]GGTACCAGCCACTGC | 57626 |
rs199700432 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70012901 | GAGCAAGATTCTGTA[A/T]AAAAAAAATAATAAT | 57626 |
rs199708021 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69754014 | CTAATTTTTTTTTTT[-/T]GTTTTTAGTAGAGAT | 57626 |
rs199710899 | in-del | -/TGTGGCTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100197 | CATATTTCTTCATTA[-/TGTGGCTC]TTTCTTCTCAGCATG | 57626 |
rs199727477 | in-del | -/TCTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001582 | TCTATGATCTATGTG[-/TCTA]TCTATCTATCTATCT | 57626 |
rs199746292 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780706 | TATATATATATGTAT[A/G]TATATATATGTATAT | 57626 |
rs199748781 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715524 | GGCAGTTTTATTATT[-/TA]TTTTTTTTTTTTTGA | 57626 |
rs199751448 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70085639 | GAGGCCGAGGCTGGA[A/G]GATCACCTGAGGTCA | 57626 |
rs199759411 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024628 | AAAAGATTTCTCTCT[A/C]TCTCTCTCTCTCTCT | 57626 |
rs199762702 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69948863 | TCTACCAGAAAAGTG[A/C]AAAAACTGCCTATAA | 57626 |
rs199764344 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027652 | CGCAAAATGTAAGTT[-/G]TTTTTTTTTTTTTAT | 57626 |
rs199778649 | snp | C/T | 1.65636e-05 | 0.00287776 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69961315 | TGCCATACCTGTATA[C/T]GCAAATTGGACAAGG | 57626 |
rs199790878 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70063981 | AAACATCAAAATTAT[A/G]CAATGTTGTTTTCAT | 57626 |
rs199800549 | in-del | -/CAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70067660 | CAACAACAACAACAA[-/CAA]AAAGGTTCTTGATGT | 57626 |
rs199803110 | in-del | -/TCTA | 0.479583 | 0.0989539 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789018 | TGGACTCCACAGGAC[-/TCTA]TCTATCTATCTATCT | 57626 |
rs199808122 | in-del | -/ATAG | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077520 | TATGATCCTAAAATA[-/ATAG]ATACATGAAATTATG | 57626 |
rs199831877 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69904168 | TTTAATAATAGAAAA[A/G]TAAAATGCATTAAGT | 57626 |
rs199838675 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084464 | CTATTTCTTCTTCTT[-/C]TTTTTTTTTTTTTGA | 57626 |
rs199858216 | in-del | -/TC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69723847 | AGTCAGAATTTTTTT[-/TC]TTTTTTTTTTTCTGA | 57626 |
rs199861631 | in-del | -/AG | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771278 | TTTAGCAACTTTCAA[-/AG]AAAAAAAAAAAAAAC | 57626 |
rs199863873 | in-del | -/TAAT | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790671 | TTTAATATACTCTAC[-/TAAT]TAATTAATTGAAAAA | 57626 |
rs199885973 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69960709 | TAATACTTGTATATT[G/T]AGTAACATTCAACAA | 57626 |
rs199917322 | in-del | -/A | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805952 | AGGCTGCTCAAGGGG[-/A]AAAAAACCCTATCAG | 57626 |
rs199924029 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69826478 | CCAGCTACTCAGGAG[G/T]CTGAGGCAGGAGAAT | 57626 |
rs199930468 | in-del | -/TATATATATG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780693 | CTTTCTTCATATATA[-/TATATATATG]TATATATATATATGT | 57626 |
rs199935217 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69740204 | TCTTTAATCATCAAT[A/T]AATGTGAAGCAATTT | 57626 |
rs199947221 | in-del | -/AAAG | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939657 | TGTGCATAAAGCCAT[-/AAAG]AAGCTTCCTGAATGC | 57626 |
rs199948287 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69968543 | TATGGGTTGAAATTT[A/T]AAAAAAAAAAAGAAA | 57626 |
rs199951431 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027396 | ACTCATGGATGAAGG[A/G]AAAAAAACAACATTC | 57626 |
rs199960335 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70006502 | AGTATTCCCCCTCAA[G/T]TTTTTTTTTTTTTTT | 57626 |
rs199969524 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958447 | AAAAGTTATTTTTTC[A/G]AAGATTATAAACTAT | 57626 |
rs199985994 | snp | A/G | 0.00011761 | 0.00766756 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69839009 | CTCCTACAGCATACA[A/G]AGTTCCGACTGTAGA | 57626 |
rs200021897 | in-del | -/TGTGTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075557 | ATATATATACCTGTG[-/TGTGTA]TGTGTGTATGTGTAT | 57626 |
rs200023465 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69943244 | GATTTCTTCATTTAA[-/T]TTTTTTTATAATTAA | 57626 |
rs200024471 | snp | A/C | 0.000148364 | 0.00861163 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107459 | AGGAAGAGGACGGGG[A/C]GGACGATGAAGAGGA | 57626 |
rs200027046 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70054825 | AAATTGATCAAGCAT[A/T]AAGAGAGAATTAGTG | 57626 |
rs200039981 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781913 | TCCCATAATTTAATA[G/T]TCATTTTATTGCTTT | 57626 |
rs200042348 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69876963 | AATCGCTTGAACCTG[C/T]GAGGCAGAGGTTGCA | 57626 |
rs200049404 | in-del | -/TT | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949933 | GGCCTCCTCTCTCTC[-/TT]GTCAGAGAGAAAATC | 57626 |
rs200052154 | in-del | -/TT | 0.0314385 | 0.121371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962067 | TTTATTTGGGGAGAC[-/TT]GACATAATTTTCATA | 57626 |
rs200052226 | in-del | -/C | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949092 | GACATATAACTGTTT[-/C]CCCCATTATTAACAT | 57626 |
rs200060670 | in-del | -/TGTGTGTGTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947029 | ATTGTGTGTGTGTGT[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 57626 |
rs200068760 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947081 | GTGTGTGTGAAGATC[A/T]TCTTCCTATTCCGTC | 57626 |
rs200077831 | in-del | -/A | 0.338296 | 0.233889 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070153 | GTGAGACTCGTCTCG[-/A]AAAAAAAAAAAGAAG | 57626 |
rs200083283 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70101951 | GCAAAAAAAAAAAAA[-/AA]CAAAGTAAAATTGAG | 57626 |
rs200083456 | in-del | -/ATATA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855855 | GGTATTATATATGTT[-/ATATA]ATATATTATATATTA | 57626 |
rs200101838 | in-del | -/A | 0.0640965 | 0.167152 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906633 | TTTATCTTGAATAAC[-/A]AATTTCTTTTAAATA | 57626 |
rs200111252 | in-del | -/A | 0.0899317 | 0.192037 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703450 | AAGAGTTTAAAAAGT[-/A]AAAAAAAAAATTACA | 57626 |
rs200121001 | snp | A/C | 0.00201653 | 0.0316891 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938038 | TTAAGGAGAAAAAAA[A/C]ACACACACAATATGT | 57626 |
rs200133800 | snp | C/T | 0.478437 | 0.10157 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813063 | ACAATAGCAAAGACT[C/T]GGAACCAACCCAAAT | 57626 |
rs200138290 | in-del | -/GAATCT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69905198 | CAACAGAATGTAATG[-/GAATCT]ACATGTTGGTTTTTA | 57626 |
rs200140393 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69997940 | GTGTCTCTTCGAGAT[C/T]CTGATTTCAATTCTT | 57626 |
rs200140442 | in-del | -/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69935204 | ACGTGGTACATAGTT[-/CA]GGTACTGGTGAACTT | 57626 |
rs200157530 | in-del | -/G | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002934 | TCATTATTTTTATTA[-/G]GGAAAATAAGATACA | 57626 |
rs200178226 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69785595 | TAAGATCACAATTAA[A/G]AACTAGAAAAGCAAG | 57626 |
rs200179379 | in-del | -/A | 0.0314385 | 0.121371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705236 | TTTCAAATCAAACAC[-/A]AAAAAATAAGCTCGG | 57626 |
rs200187987 | snp | G/T | 0.462691 | 0.131387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804306 | AAATATAATTTTTTT[G/T]TGGGGGGGGGAAATA | 57626 |
rs200195888 | in-del | -/TG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780715 | ATGTATATATATATA[-/TG]TATATATATATATAT | 57626 |
rs200197480 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026712 | ACTTAGGGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 57626 |
rs200204787 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69763930 | AACCTGAAGTAACCA[-/T]TTTTTTTTTCTATTG | 57626 |
rs200211825 | in-del | -/TAAA | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054279 | TATCTTGGTAAACTT[-/TAAA]TAATACAAATCGAAT | 57626 |
rs200211962 | in-del | -/TTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69753842 | CATAGAAATAATTGA[-/TTG]AAAAAAAAATTTTGA | 57626 |
rs200227838 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789373 | TACATTATTATTTAC[-/T]TTTTTTTTGGCAACA | 57626 |
rs200228855 | in-del | -/AAGT | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723476 | AATAACAAAAAAAGA[-/AAGT]AAGCCCAGGACCAGA | 57626 |
rs200231598 | in-del | -/TATATATATATATGTATATATATATATG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780689 | TTCTCTTTCTTCATA[-/TATATATATATATGTATATATATATATG]TATATATATATATAT | 57626 |
rs200234321 | in-del | -/TG | 0.0205511 | 0.0992634 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786173 | AGGCCAGCATCATCC[-/TG]TGATACCAAAGCCTG | 57626 |
rs200238012 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70088565 | TGTATGCCTATATCT[-/A]CCAGCTATTTAGGAT | 57626 |
rs200243442 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69877905 | AATAAAGAATATCTG[A/C]TTTTCTCTGTGTACT | 57626 |
rs200244673 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69783939 | CAGAGAGAAAGGAAG[A/G]TCGGGTTACCCACAA | 57626 |
rs200247243 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69960111 | TCAGAGCATGTGTAC[-/T]TTTTTTTTTTTTTTT | 57626 |
rs200260761 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020786 | TTGTCTTCATATTGT[G/T]AGATATATATGTATA | 57626 |
rs200270716 | in-del | -/T | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819874 | TTTGAGAGTCTCAGC[-/T]TTTTAATTGGTTTAC | 57626 |
rs200270848 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69774675 | TAATAAAAAAAAACA[G/T]ACACACACAAGCAAG | 57626 |
rs200270928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966948 | TGACATGATTTCATT[G/T]TTTTAATGGCTGAAT | 57626 |
rs200272608 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69843282 | AAGACAAAAAAATAG[-/A]AAAAAAAATTAGAAA | 57626 |
rs200273416 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69914472 | AGGAATAATCCAGGG[A/G]ATTTTCTGCTAAGGC | 57626 |
rs200280955 | in-del | -/A | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956174 | GATATATATATTTAT[-/A]TATATATCTGATATA | 57626 |
rs200292582 | in-del | -/TTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69926309 | CTTAAGTTATTTAAA[-/TTG]AAGCATATATTAAAT | 57626 |
rs200293561 | snp | C/T | 0.00170215 | 0.0291235 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719341 | TTGCACTGTCTCTTT[C/T]GCTGTAACAGTGTCC | 57626 |
rs200293697 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69808559 | AACAGAATAAAAAAA[-/T]CAAGAAGTCACATCC | 57626 |
rs200298420 | in-del | -/AT | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858489 | TTTCTCCTTGTAAAA[-/AT]ATGAGTTAAAGTGAT | 57626 |
rs200299937 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69751926 | TAAGAGGATGTATTT[A/C]TTTGCTTACACTCCT | 57626 |
rs200300939 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69904169 | TTAATAATAGAAAAA[A/T]AAAATGCATTAAGTT | 57626 |
rs200306786 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70042936 | TATGAGACTGAGTCT[A/C]ACTCTGTTGCCCAGG | 57626 |
rs200313025 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69738095 | CTCCAGGGGCGGGAC[A/G]GACCCAGGCAGATAG | 57626 |
rs200321182 | snp | A/G | 0.160609 | 0.233472 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840698 | TTTATATATATATAT[A/G]TATGTATGTATGTAT | 57626 |
rs200326251 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69793496 | CTCATAAAATCATGT[A/T]AGTTTTTTTTTTACA | 57626 |
rs200329193 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69740668 | TAACATAATAAAATG[-/A]AAAAAAATTAAAAAT | 57626 |
rs200330962 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70063714 | GAATTTATTCTAATA[-/T]TTTTTTTAAAAAATG | 57626 |
rs200339697 | in-del | -/GTAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69840737 | TATGTATGTATGTAT[-/GTAT]AGAAGATCTCCAATG | 57626 |
rs200342913 | in-del | -/TATATG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780711 | ATATATGTATATATA[-/TATATG]TATATATATATATAT | 57626 |
rs200344764 | in-del | -/GAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855302 | TTAGATAGATAGATA[-/GAT]GATAGATAGATAGAT | 57626 |
rs200350455 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69840693 | TAACTTTATATATAT[-/AA]ATATATATGTATGTA | 57626 |
rs200355649 | in-del | -/AC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69813469 | AAAATACACACATAT[-/AC]ATACACACACATACA | 57626 |
rs200357535 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69845265 | GTATAATAAAGTCTG[C/T]TTGCTTATTACAAAA | 57626 |
rs200359109 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69731445 | CATCACTATAGGCTG[G/T]GTATGATTTTAACTC | 57626 |
rs200366470 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69981787 | GTTCAAAAAGTGCCC[-/A]AAAATAAAAAAAAAT | 57626 |
rs200369040 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022810 | GCCTAAGCCTTTTTT[-/TA]ATGCCTTAATCTCAT | 57626 |
rs200371345 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70019366 | GGACCTTCATTAACT[C/T]TTATAGCTTACTCAG | 57626 |
rs200392885 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075440 | TCCCACAAAATTTTA[-/T]TTAAAAAAAACCTTT | 57626 |
rs200397778 | in-del | -/A | 0.39474 | 0.203839 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959558 | TTCAGACTACTCATT[-/A]AAAAAAAAAAACATG | 57626 |
rs200400075 | in-del | -/CCTATG | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789096 | ATCCATCTGTCTATA[-/CCTATG]CCTATATTAAAATCT | 57626 |
rs200405861 | in-del | -/CAGA | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873619 | ATTTCTCTCACATTC[-/CAGA]CAAATAACATATCAA | 57626 |
rs200406438 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69841442 | AGTTGAGAAAAAAAA[A/T]CAAGTAGTCCATTTT | 57626 |
rs200412180 | in-del | -/GAGAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69878725 | ATAGAGAGAGAGAGA[-/GAGAG]AGAGAGTGAGAGAGA | 57626 |
rs200412739 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70003175 | CATACAAACTACAAA[A/T]AAATCTTTTCTCCAT | 57626 |
rs200414462 | in-del | -/T | 0.0287284 | 0.116357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968540 | TATTATGGGTTGAAA[-/T]TTAAAAAAAAAAAAG | 57626 |
rs200417344 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837679 | GTGTGTGTATATATA[C/T]ATATATATACACATA | 57626 |
rs200422196 | in-del | -/CA | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995890 | AGGTCTCGACCCACA[-/CA]GAGTCAGGTGTATTA | 57626 |
rs200428292 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69745043 | AAAAAGCTTTCCAGG[-/T]TTTTTTTTTAACCAA | 57626 |
rs200432953 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949199 | TTTACATTCCTTAGA[-/T]TTTTTTTTTCTTTTC | 57626 |
rs200438280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882271 | TATTTAAACAGCGTC[A/G]CACATCATTACCTGT | 57626 |
rs200445287 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69712760 | TTTTGTTTGTTTTTT[G/T]TTTTTTTTTTTTGGG | 57626 |
rs200445733 | in-del | -/ACAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69774672 | ACTTAATAAAAAAAA[-/ACAC]ACACACACAAGCAAG | 57626 |
rs200451937 | in-del | -/AAC | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991380 | AGTTGGTTCTTTGAA[-/AAC]AACAACAATGACAAC | 57626 |
rs200452178 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69771279 | TTAGCAACTTTCAAA[-/G]AAAAAAAAAAAAACA | 57626 |
rs200452974 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69752887 | GAATACAGCCTCTCC[A/G]CATCCACTGCTGCCT | 57626 |
rs200461804 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802809 | GACAGGAGTCTTGCC[A/G]ATGCTCCCGGCTGAA | 57626 |
rs200473264 | in-del | -/AA | 0.121717 | 0.214577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010106 | CTAGAGTGGAAGAAC[-/AA]AAGAGAGTGCAATAG | 57626 |
rs200481538 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69945462 | TCTAGTTAAAAGAAA[A/G]AAAAAAAAAAAGCCA | 57626 |
rs200493457 | in-del | -/T | 0.0178098 | 0.0926698 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988082 | ATAATACTAAATAGC[-/T]TTTTTTTGGCGGGGG | 57626 |
rs200494625 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69882642 | AGAAACTAGAGGCTG[G/T]TAAGATGAAAGCATT | 57626 |
rs200504320 | in-del | -/TTTG | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920136 | CAAATATAGATAAAA[-/TTTG]TTTGTTTTTGGCTCT | 57626 |
rs200509698 | in-del | -/TGTGTGTGTGTGTGTA | 0.177503 | 0.239258 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022290 | GTGTGTTTGTGTGTG[-/TGTGTGTGTGTGTGTA]TGTGTTTGGTTGTAG | 57626 |
rs200511575 | in-del | -/TATATG | 0.156319 | 0.231784 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736685 | AGATTGTGAGATATA[-/TATATG]TATATATATATACAC | 57626 |
rs200511610 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69742513 | CTTTATGTGTCAGGA[A/C]TTATTATTGGCACCG | 57626 |
rs200511679 | snp | A/G | 6.61978e-05 | 0.00575278 | missense | KLHL1 | GRCh38.p7 | 13:69961352 | AGAGCATTGGGGTCT[A/G]TGCCTTCCATTTTGA | 57626 |
rs200516143 | in-del | -/AGCACAAGAAT | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716337 | CCAGAAATTGTACCA[-/AGCACAAGAAT]ATAGAGATGGGTGGA | 57626 |
rs200525992 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020804 | ATATATATGTATATG[C/T]ATACATACACATACA | 57626 |
rs200533616 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69969942 | ATCGATTAAACTTTT[G/T]AAGTTCCACTTCAAT | 57626 |
rs200543686 | in-del | -/TTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715523 | AGGCAGTTTTATTAT[-/TTA]TTTTTTTTTTTTTGA | 57626 |
rs200544811 | snp | A/C | 1.64969e-05 | 0.00287196 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107341 | AGTGACTCCACGTAG[A/C]AGAGAGTCCTGGCTG | 57626 |
rs200547756 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69756909 | AAAAGTGTCACTAAG[A/G]TTATCCTTTGCAAAT | 57626 |
rs200554749 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020783 | ATTTTGTCTTCATAT[A/T]GTGAGATATATATGT | 57626 |
rs200570961 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69954927 | GATTTTATTTTTATT[A/T]CTTTTATTTTGTTAC | 57626 |
rs200586157 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038580 | TTTGGGATTGTCATT[A/T]ATTTTTTTTTTTTTT | 57626 |
rs200586321 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70004523 | TATCCTGCCATCCCC[C/T]TGACTAGTCCACGTT | 57626 |
rs200594227 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69920113 | TGTATTATTATAATT[C/T]TCTGACTCAAATATA | 57626 |
rs200625045 | in-del | -/C | 0.021354 | 0.101099 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938038 | TAAGGAGAAAAAAAA[-/C]ACACACACAATATGT | 57626 |
rs200625187 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996910 | TATTTTATTCATTAA[A/T]TTTTTTTTTTTTTTT | 57626 |
rs200631715 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69943676 | ATCTGCTGTTATAAA[A/G]ATAAAGTTAAAATAG | 57626 |
rs200631789 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026856 | AACAAAGTATATATT[A/T]AAAAAAGACAAATAG | 57626 |
rs200644712 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70076387 | TGAGGAAAGGATAAT[C/T]TTTTTTTTTTTTTTA | 57626 |
rs200646320 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951365 | TAGAAGGGAGATAGA[A/C]AGTGGTAAGTATAAA | 57626 |
rs200646438 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027183 | CTGTATTTGTGGCTG[G/T]TTTTAAAAGTATAAC | 57626 |
rs200660318 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69878698 | TATATGTGTGTATGC[-/AT]ATATATATATATAGA | 57626 |
rs200679956 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69934984 | TATATATATATATAT[A/G]TATATGTATATATAT | 57626 |
rs200683978 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69942463 | TAGATTTCTCCTTTT[C/T]ATCATGAATAGTTTT | 57626 |
rs200684299 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022813 | TAAGCCTTTTTTTAA[-/T]GCCTTAATCTCATGC | 57626 |
rs200692477 | in-del | -/TA/TATA | 0.261915 | 0.250494 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985910 | TATATATATGTAAGT[-/TA/TATA]TATATATATATGTAA | 57626 |
rs200701494 | in-del | -/TGTGTGTGTGTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947029 | ATTGTGTGTGTGTGT[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 57626 |
rs200702701 | snp | C/T | 1.70153e-05 | 0.00291674 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740586 | AAATGAATGTAGTGC[C/T]TATAGTTAATATCAT | 57626 |
rs200707179 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70019365 | ACTGAGTAAGCTATA[A/G]AAGTTAATGAAGGTC | 57626 |
rs200709449 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947079 | GTGTGTGTGTGAAGA[A/T]CTTCTTCCTATTCCG | 57626 |
rs200710973 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715527 | AGTTTTATTATTTAT[A/T]TTTTTTTTTTTGAGA | 57626 |
rs200731019 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69841433 | AACAATCTAGTTGAG[-/A]AAAAAAAAACAAGTA | 57626 |
rs200732755 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922118 | ATTTATTTGCCTTCC[-/T]TTTTTTTTAATATAA | 57626 |
rs200755377 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69755644 | TCATCTCCAAAGTAA[-/T]TTTTAAAAAAAAAGC | 57626 |
rs200789436 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915600 | AATTAATTCAAGATG[C/G]ATTAAAGACTTAAAT | 57626 |
rs200795136 | snp | A/G | 0.138546 | 0.223781 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919553 | TGGGTACATTAATGA[A/G]ACCAATTTTCTCTCC | 57626 |
rs200797781 | in-del | -/A | 0.497749 | 0.0334707 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961223 | TACAGAATTTTTTTT[-/A]AAAAAAGCGTTAAAT | 57626 |
rs200806388 | in-del | -/TAAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69982473 | TAATAATAATAATAA[-/TAAT]AATAAAATAAAAAGC | 57626 |
rs200811617 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69903630 | ACCCTTGTTCACATT[C/T]TTTTTTTTTTTTTTT | 57626 |
rs200812625 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69849738 | AATCAGAAAAAAAAA[C/T]CTGCTATTTATTGTT | 57626 |
rs200816876 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69825999 | TTACAGAAAAAAAAA[-/G]ATTTATTTATTTTGT | 57626 |
rs200817761 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69847423 | AAAAAAAAAAAAAAA[A/T]AAAACATAATTTAAA | 57626 |
rs200821332 | in-del | -/CAAATCTGGGC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69759104 | CTCCCAGCAGGGAGG[-/CAAATCTGGGC]CGAGGAAGATGGGTC | 57626 |
rs200839979 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69890237 | CTGCAATAACAATTT[C/T]CAAAAAAAGAAAATG | 57626 |
rs200848678 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69720987 | CCAAATCACTAAAGC[A/C]AAAGGGAAGTCAAGC | 57626 |
rs200868651 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69988281 | CCTTCCATGTTCCTG[C/T]AAGGACATGACCTCA | 57626 |
rs200883126 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69793497 | TCATAAAATCATGTA[A/G]GTTTTTTTTTTACAT | 57626 |
rs200890874 | in-del | -/TAGATAGATAGATAGA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855289 | CACTCGTACTAATTT[-/TAGATAGATAGATAGA]TAGATAGATAGATAG | 57626 |
rs200895908 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011101 | GGGTCAGATCACCCA[A/G]TGACTACCTGTACCA | 57626 |
rs200905037 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961828 | GAGATTTCTATTATG[G/T]TTTATTTGCCTGTTC | 57626 |
rs200911842 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020784 | TTTTGTCTTCATATT[G/T]TGAGATATATATGTA | 57626 |
rs200920987 | in-del | -/T | 0.0908922 | 0.192833 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706153 | CATTACTTGCTTTTA[-/T]TTTTTTTTTTACATA | 57626 |
rs200922185 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69983916 | TGATTTTTGACAAAG[A/G]TCCCACAGTAAATGA | 57626 |
rs200924728 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837681 | GTGTGTATATATATA[C/T]ATATATACACATATA | 57626 |
rs200926053 | in-del | -/A | 0.0410537 | 0.137264 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818113 | TCATCTGACAGCCTT[-/A]TTTTATTCTTGGATT | 57626 |
rs200945294 | in-del | -/GTTTC | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942155 | ACTAAAGCTTGAATT[-/GTTTC]ATTTATATTTTCATT | 57626 |
rs200946136 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020788 | GTCTTCATATTGTGA[G/T]ATATATATGTATATG | 57626 |
rs200948812 | in-del | -/C | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898979 | CTAAAGGAATTTGGT[-/C]AGCTGCAATTGATAT | 57626 |
rs200953427 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69958316 | TCTGAAAAACCTGAT[C/T]TCATTGCTTCTCATC | 57626 |
rs200953553 | in-del | -/A | 0.333491 | 0.235646 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806633 | CAGAGCTCAGAAATC[-/A]GCTTTAACAATCTGG | 57626 |
rs200961680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860172 | TGTTAAGTGTCTATT[A/G]ATCTTCAGTACTACA | 57626 |
rs200970113 | in-del | -/TTTCTTCATTATGTGGCTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100186 | TATTATATATTCATA[-/TTTCTTCATTATGTGGCTC]TTTCTTCTCAGCATG | 57626 |
rs200973987 | in-del | -/AC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69791049 | ATTGCTGTGGGGGAA[-/AC]ACACACACACACACA | 57626 |
rs200976141 | in-del | -/AT/ATAT/ATATAT | 0.146678 | 0.237802 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833832 | CACACACATGTATAC[-/AT/ATAT/ATATAT]ATATATATATACACA | 57626 |
rs200980454 | in-del | -/ATTATATGA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69846825 | CAGCTTTCCAAGAGT[-/ATTATATGA]TTTTATTTGAAATGT | 57626 |
rs200980634 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70092846 | TAGAGGAGTAGCCAC[A/G]CTTTCAGTGCTTGAT | 57626 |
rs200994839 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69748108 | AAACATATAAATATT[-/A]GAAAGATTTATATAT | 57626 |
rs200996749 | in-del | -/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69899019 | AATAAAAATTACACA[-/TT]TTTTTTTTTTTTTGT | 57626 |
rs200998641 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090613 | CACGATGATATAGGG[-/AGA]AGAAGTCAGAAAGGT | 57626 |
rs201018416 | in-del | -/GTGTGAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947070 | TGTGTGTGTGTGTGT[-/GTGTGAA]GATCTTCTTCCTATT | 57626 |
rs201021544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960706 | AATTAATACTTGTAT[A/G]TTGAGTAACATTCAA | 57626 |
rs201028771 | in-del | -/TG | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823525 | AGAAATTGGACTAGA[-/TG]TATATACACACACAT | 57626 |
rs201044307 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69803550 | TGAAATATCAGTCCA[C/T]GAACGGCTACGCTAT | 57626 |
rs201047091 | in-del | -/CG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855839 | AAAATATTATATATA[-/CG]GTATTATATATGTTA | 57626 |
rs201047725 | in-del | -/GAGC | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943426 | ATGAAGGAAAAAGAA[-/GAGC]GAGCAGATACACTGC | 57626 |
rs201048595 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868022 | AACAAAAAACAAAAT[A/G]ATAAGTTTTGATAAT | 57626 |
rs201066043 | in-del | -/TA/TGTA | 0.256897 | 0.249905 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075559 | ATATATACCTGTGTG[-/TA/TGTA]TGTGTATGTGTATAT | 57626 |
rs201071800 | in-del | -/C | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780856 | TTTAACATCACATTT[-/C]CCCCATGTGGTTTAT | 57626 |
rs201073244 | in-del | -/TATATATG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780695 | TTCTTCATATATATA[-/TATATATG]TATATATATATATGT | 57626 |
rs201075630 | snp | C/T | 3.30674e-05 | 0.00406603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882249 | GGGTTTTTCAGTACA[C/T]TGAATCTATTTAAAC | 57626 |
rs201084853 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972923 | AGGTAGCCTACCTAT[-/A]AAAAAATTTTTGATG | 57626 |
rs201089333 | in-del | -/G | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996616 | CTAAAGGGGAGAAAA[-/G]CTTCACTTCAATGTT | 57626 |
rs201110976 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69968554 | ATTTAAAAAAAAAAA[A/G]GAAATTGAAGGTATT | 57626 |
rs201124904 | in-del | -/CT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69822954 | TTTATGTTTTTATAA[-/CT]CAACTTATTTTGCTC | 57626 |
rs201140611 | snp | C/T | 0.000148447 | 0.00861404 | missense | KLHL1 | GRCh38.p7 | 13:69719445 | CTGCATAAAGAAAAC[C/T]GTCACATGTGGCCAC | 57626 |
rs201146874 | in-del | -/TCTATCTATCTATCTATCTATCTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789018 | TGGACTCCACAGGAC[-/TCTATCTATCTATCTATCTATCTA]TCTATCTATCTATCT | 57626 |
rs201149745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703842 | TCATACAGCCTCAGT[A/G]TGTAGTAGGCCATAC | 57626 |
rs201160848 | in-del | -/A | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824918 | TTGCCTAAAATATCT[-/A]AAAAAAAATTTGAAA | 57626 |
rs201167167 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039057 | TATATCCTTTGCACA[-/T]TTTTTTTTTTTTTTT | 57626 |
rs201191590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772143 | TTTTAATAGAGTTGG[A/G]GTTTCACCATGTTGG | 57626 |
rs201193136 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804306 | AAATATAATTTTTTT[-/G]TGGGGGGGGGAAATA | 57626 |
rs201203188 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804297 | TATGTAGACAAATAT[-/A]ATTTTTTTGTGGGGG | 57626 |
rs201207802 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69911569 | AGGAATATCATCAAG[A/G]AAAAAAAAAAAAAAG | 57626 |
rs201210738 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901904 | ACGGGTTCAAGCGAT[A/T]CTCCTGCCTCAGCCT | 57626 |
rs201212735 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060550 | AGACAAAAAAAAAAA[-/T]GTGGTATATATAGGC | 57626 |
rs201215445 | in-del | -/AATT | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862679 | AGCCTTTAAGGAGAC[-/AATT]AATACTAAATGAGGT | 57626 |
rs201238671 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780743 | ATATACATATATATA[C/T]ACATATATATATATA | 57626 |
rs201241520 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69818219 | TTAACTCATAGGCAT[C/T]TTTTTTTTTTTTTTT | 57626 |
rs201251534 | in-del | -/AAATAG | 0.0209421 | 0.100162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731068 | AGAAAATGTGAATAT[-/AAATAG]AAAAAGTAGTATTAA | 57626 |
rs201260904 | in-del | -/C | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949322 | AAGTTTTCAGACTTT[-/C]CTTTTTTTAATGATT | 57626 |
rs201265781 | in-del | -/AT | 0.26078 | 0.249767 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985847 | TATGTGTGTGTATAG[-/AT]ATATATATATACATA | 57626 |
rs201267024 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69958457 | TTTTCAAAGATTATA[A/G]ACTATAATCATTGAA | 57626 |
rs201274470 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69886389 | ACCAGTTTTTTTTTT[-/G]TTTGTTTAATTATTT | 57626 |
rs201275656 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70097899 | TCTGTTTTTTTTTTT[C/T]CAATTTTAATAGGCT | 57626 |
rs201282265 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70061352 | CCATTTTTTTTTTTT[-/T]CTGACTAGTAACATG | 57626 |
rs201288356 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69877474 | ACTATATATATATAT[-/A]TTTTTTTTCAGTCAT | 57626 |
rs201293197 | in-del | -/ATTATT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69760370 | ATTATTATTATTATT[-/ATTATT]TTGAGACGGAATTTC | 57626 |
rs201294199 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075776 | ATATATATATATACA[C/T]ATATATGTATATATA | 57626 |
rs201297570 | in-del | -/A | 0.0220767 | 0.102718 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821092 | TAAAATTTGAATTTT[-/A]AAAAAATAAAAATTT | 57626 |
rs201298175 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814850 | ACCCCGTCTCTACTA[A/C]AAATACAAAAATTAG | 57626 |
rs201300102 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70006518 | TTTTTTTTTTTTTTT[C/T]AAAGAGTTTGAGAAG | 57626 |
rs201311691 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69751928 | AGAGGATGTATTTCT[G/T]TGCTTACACTCCTCC | 57626 |
rs201313749 | snp | A/C | | | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107392 | GGAGCCCCTTGCTGC[A/C]GCCTCGTGGCAACTG | 57626 |
rs201315533 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69988092 | TAGCTTTTTTTTGGC[-/G]GGGGGGAACCTCTCC | 57626 |
rs201318069 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70010902 | CGTCTCAAAAAAAAA[-/T]AATAATAATAATAAA | 57626 |
rs201320816 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69928785 | AATGGAGAGCGAATA[A/G]GTAGAGGTATCTTGG | 57626 |
rs201323073 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69805173 | CTAAATCATTATAAT[-/AA]TCCAAATGTGCCAAA | 57626 |
rs201323322 | snp | A/G | 3.65865e-05 | 0.0042769 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107617 | GCCGGGCCGCCGGTG[A/G]AAGGAGACGGGTGGC | 57626 |
rs201336365 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734500 | TCTGAATTTAAAGAC[C/T]AGTAAGTAGAACTAA | 57626 |
rs201347400 | in-del | -/TATATATATATATATATATATG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69934969 | GTGCATGTGTATATA[-/TATATATATATATATATATATG]TATATATATACATAT | 57626 |
rs201352752 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69743723 | CCTGGGAGGCAGAGG[A/T]TGCAGTGAGCCAAGA | 57626 |
rs201355500 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706241 | AAGACTTAGATCTCT[G/T]GATATTTCCCCTTCT | 57626 |
rs201380542 | in-del | -/TATAT | 0.297128 | 0.245518 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855861 | ATATATGTTATATAA[-/TATAT]TATATATTATATATG | 57626 |
rs201387969 | in-del | -/AG | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734656 | AGTGATAATACTAAC[-/AG]AGAAAAATAACAAAT | 57626 |
rs201394429 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69808870 | TATTGGAAAGAACCA[A/G]ACAGATTTTCTGCAA | 57626 |
rs201398447 | in-del | -/GTCT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789271 | CATGTCTGTCTGTCT[-/GTCT]TTTATTTTGTATGGG | 57626 |
rs201401666 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020787 | TGTCTTCATATTGTG[A/G]GATATATATGTATAT | 57626 |
rs201410671 | in-del | -/TG | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833658 | AGACATTTGCACATA[-/TG]TGTGTTTATAGCAAC | 57626 |
rs201415071 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70017637 | GTAGGCAGAATGAGC[A/C]CAGCAGGTATGAGCA | 57626 |
rs201428551 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69951319 | AGTGGCTTATTTTTT[-/C]TTTCCTTTATATTCT | 57626 |
rs201439192 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69845266 | TATAATAAAGTCTGC[C/T]TGCTTATTACAAAAC | 57626 |
rs201441291 | snp | G/T | 0.472016 | 0.114931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804307 | AATATAATTTTTTTG[G/T]GGGGGGGGGAAATAG | 57626 |
rs201448333 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70063514 | CCATGTTATTTTGTT[A/T]TTTAAAATTATAATC | 57626 |
rs201448660 | in-del | -/TTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69978489 | ATTCTGGTCAGAATA[-/TTT]TTTTTTTTTTTTTGA | 57626 |
rs201450783 | snp | A/G | 1.98391e-05 | 0.00314947 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975846 | CACAAAATAATAAAG[A/G]GATTTATAAAGAGCC | 57626 |
rs201453530 | in-del | -/GTGTGTGAGAGA | 0.358728 | 0.225118 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719204 | TGTGTGTGTGTGTGT[-/GTGTGTGAGAGA]GAGAGAGAGAGAGAG | 57626 |
rs201460791 | in-del | -/TGTGTGTGTGTGTGTGTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947029 | ATTGTGTGTGTGTGT[-/TGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 57626 |
rs201461851 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024622 | GAGGAGAAAAGATTT[A/C]TCTCTCTCTCTCTCT | 57626 |
rs201467148 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947080 | TGTGTGTGTGAAGAT[C/G]TTCTTCCTATTCCGT | 57626 |
rs201485154 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69903900 | TTGCCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC | 57626 |
rs201487406 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69962685 | TGATATTTTAGAATG[-/A]AAAAAATTATGATAT | 57626 |
rs201490284 | in-del | -/TTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69964054 | TGTCAGTTTGTTTGT[-/TTG]TTTTTTAAAAATAGG | 57626 |
rs201493200 | in-del | -/TATG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780713 | ATATGTATATATATA[-/TATG]TATATATATATATAT | 57626 |
rs201503600 | in-del | -/TA | 0.0193772 | 0.0965046 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814356 | CAAATAATGTATTAC[-/TA]TGTCCTGAAAAGCAA | 57626 |
rs201508057 | in-del | -/AGATAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855382 | GAGAGATAGATCTAT[-/AGATAG]AGATAGAGATAGATA | 57626 |
rs201508879 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70031397 | AAGTCTCTGGATGAG[-/A]AAAAAAAATAATGTT | 57626 |
rs201518335 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026714 | TTAGGGTGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 57626 |
rs201525188 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911588 | AAAAAAAAAAAGCCC[-/A]AAGCACTAATAGTAA | 57626 |
rs201532303 | in-del | -/ATG | 0.0752113 | 0.178743 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936009 | TGTATAAGAAAGTTT[-/ATG]ATATCACACAATCCT | 57626 |
rs201532524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719320 | TGAATCAGGCATCAA[C/T]GTGATTTGCACTGTC | 57626 |
rs201537222 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70021336 | GGCTTTTCATGGCTT[A/C]ATAGGCCACTTCTTT | 57626 |
rs201540320 | in-del | -/GTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69964044 | GGAATTTTTTTGTCA[-/GTTT]GTTTGTTTGTTTTTT | 57626 |
rs201543842 | in-del | -/TTTTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69723844 | GCCAGTCAGAATTTT[-/TTTTC]TTTTTTTTTTTTTTC | 57626 |
rs201551864 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855341 | AGATAGATAGATAGA[C/G/T]AGATAGACAGACAGA | 57626 |
rs201554162 | in-del | -/TT | 0.0260105 | 0.111035 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782133 | GTTTTAAGCTCTCTC[-/TT]GGAAGATGAATTATG | 57626 |
rs201557969 | in-del | -/TATATATATATGTATATATATATATG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780691 | CTCTTTCTTCATATA[-/TATATATATATGTATATATATATATG]TATATATATATATAT | 57626 |
rs201572831 | in-del | -/A | 0.489599 | 0.0713593 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073558 | AACTTAAAGTGTAAT[-/A]AAAAAAAAAATGTAG | 57626 |
rs201579262 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038581 | TTGGGATTGTCATTA[A/T]TTTTTTTTTTTTTTT | 57626 |
rs201581887 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69960708 | TTAATACTTGTATAT[A/T]GAGTAACATTCAACA | 57626 |
rs201584433 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001614 | CTATCTATCTATCTA[C/T]CTACCTATCATCTTT | 57626 |
rs201588206 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69960711 | ATACTTGTATATTGA[G/T]TAACATTCAACAAAT | 57626 |
rs201595052 | in-del | -/A | 0.0752113 | 0.178743 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996300 | AGCGAGACTCCGTTT[-/A]AAAAAAAATAAAATA | 57626 |
rs201601494 | snp | A/T | 1.78742e-05 | 0.00298945 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839198 | CTGTTAATAATGTTT[A/T]CAAAGAGATGAACAT | 57626 |
rs201607680 | in-del | -/TTTTC | 0.363776 | 0.222609 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901791 | TCTTTCTTTTTCTTT[-/TTTTC]TTTTTTTTTTTTTTT | 57626 |
rs201612481 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69717494 | TGCACTCCTATAACT[A/C]AAAATAGCCATGCTT | 57626 |
rs201619993 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69983917 | GATTTTTGACAAAGA[C/T]CCCACAGTAAATGAT | 57626 |
rs201622116 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69748794 | AGGATGGTCTGTCTT[A/G]GGGGTGGTCACTAAA | 57626 |
rs201630782 | in-del | -/AACTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69784318 | ATAATGACAGGACCA[-/AACTC]AACTCACACATAACA | 57626 |
rs201636459 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69743824 | CAAAACAAAAAAACA[A/G]AAAAAAAAAAAAAAC | 57626 |
rs201643040 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022602 | ATTTGTTTTTAAATT[A/T]TTACTATTTACATGA | 57626 |
rs201649882 | in-del | -/TTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901967 | TTGCTCAGCTAATTT[-/TTC]TTTTGTATTGTTAGC | 57626 |
rs201650587 | in-del | -/TATAAA | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002778 | TGCTAACGTGCTAAG[-/TATAAA]AAGCAAAACTATTAA | 57626 |
rs201655110 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024039 | AGTTTAATTAGTTGC[-/A]AAAAAAAATGTATTA | 57626 |
rs201660365 | in-del | -/TATATATATATG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780705 | ATATATATATATGTA[-/TATATATATATG]TATATATATATATAT | 57626 |
rs201671196 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69968340 | GAACTGATATATTTG[C/G]TAAGAAACAAATATA | 57626 |
rs201678670 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69828233 | ATGTGAGAGGGGAAA[C/T]TCAGCCTCCAAGTAC | 57626 |
rs201683214 | snp | C/T | 4.94882e-05 | 0.0049741 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69719458 | ACCGTCACATGTGGC[C/T]ACTCCGACACCCCCT | 57626 |
rs201688455 | snp | C/T | 0.104859 | 0.203554 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813503 | ACACACACACACACA[C/T]ATATATATATATATA | 57626 |
rs201690127 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69956157 | ATATATTTATATATA[C/T]TTGATATATATATTT | 57626 |
rs201701780 | snp | A/G | 0.00199802 | 0.0315439 | splice-donor-variant | KLHL1 | GRCh38.p7 | 13:69796736 | ATAAAGTAAGATCTT[A/G]CCTAGACCATGTCTG | 57626 |
rs201709305 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961825 | GGTGAGATTTCTATT[A/T]TGTTTTATTTGCCTG | 57626 |
rs201709645 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071597 | TGACCTTAACGAATC[-/A]AAAAAAAGAAAAAAA | 57626 |
rs201732105 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69709666 | AAATAAAGTCATTAT[-/TA]TTTTGTTTGTTTCTG | 57626 |
rs201736411 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69820279 | CCCCATAACAGGGTT[A/C]ACATATCGGTTATCA | 57626 |
rs201736835 | in-del | -/CTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789063 | TATCTATCTATCTAT[-/CTA]CTTATTTACCTACAT | 57626 |
rs201753394 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69751921 | CAAATTAAGAGGATG[A/T]ATTTCTTTGCTTACA | 57626 |
rs201759486 | snp | A/C | 0.00164628 | 0.0286431 | missense | KLHL1 | GRCh38.p7 | 13:69796796 | TGTCTTGGTTTTGGG[A/C]TTGTAACATTCAACA | 57626 |
rs201759895 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69969943 | TCGATTAAACTTTTT[A/T]AGTTCCACTTCAATT | 57626 |
rs201763218 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69982476 | TAATAATAATAATAA[-/T]AATAAAATAAAAAGC | 57626 |
rs201764589 | in-del | -/T | 0.0463947 | 0.145069 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700108 | GATATTACCCTATTA[-/T]TTTTTAGCTATAATG | 57626 |
rs201767051 | in-del | -/T | 0.0295035 | 0.117819 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981792 | AAAAAGTGCCCAAAA[-/T]AAAAAAAAATCTAAA | 57626 |
rs201768773 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69943677 | TCTGCTGTTATAAAA[A/T]TAAAGTTAAAATAGA | 57626 |
rs201808253 | snp | A/G | 0.494855 | 0.0504572 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812917 | GGAAGACAGTGTGGC[A/G]ATTCCTCAGGGATCT | 57626 |
rs201816677 | in-del | -/AC/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69862277 | TTACACACACACACA[-/AC/CA]GGAGAAGAGAGAGAG | 57626 |
rs201816853 | in-del | -/ATAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69774368 | ACTTGTTAAACTTTA[-/ATAT]ATTATATTTTTGTAT | 57626 |
rs201819769 | in-del | -/TTAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715519 | TCTAAGGCAGTTTTA[-/TTAT]TTATTTTTTTTTTTT | 57626 |
rs201826905 | in-del | -/ACATAGAGTGGG | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832843 | ACAAAGGAAACAAAA[-/ACATAGAGTGGG]GAAAGGACAACCTAT | 57626 |
rs201844007 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075762 | ACACATACACACACA[C/T]ATATATATATACATA | 57626 |
rs201850334 | in-del | -/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69866943 | TCTGACCTAAATTAT[-/CA]CACGTTTAATCATTA | 57626 |
rs201851170 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69793498 | CATAAAATCATGTAA[G/T]TTTTTTTTTTACATA | 57626 |
rs201880893 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70071477 | AAAATAGTGGTTGAA[C/T]TAAATAACAGCATCT | 57626 |
rs201880902 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993683 | TAGTAATGGACTCCA[-/T]TTTTTCTCATCTGGA | 57626 |
rs201882029 | snp | A/G | 1.6531e-05 | 0.00287493 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69707688 | GTATGTCTGTCCATC[A/G]TAGCCACCAACAGCA | 57626 |
rs201915169 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69870437 | GTAGCAAATTTCAAC[A/G]TGAGTTTTTGGGGGA | 57626 |
rs201921341 | in-del | -/TTAG | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863941 | GTACATAATAAGCAA[-/TTAG]TTAGTTATTAATAAT | 57626 |
rs201923463 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69958459 | TTCAAAGATTATAAA[C/T]TATAATCATTGAAGC | 57626 |
rs201923707 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69890246 | CAATTTCCAAAAAAA[-/G]AAAATGTTTGTAATA | 57626 |
rs201928389 | in-del | -/TTAAT | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938341 | AGTCTAAGAAATAAA[-/TTAAT]TTAGAGTCATTCAGA | 57626 |
rs201932480 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69959658 | TTTACAACCCGTAAC[-/T]TTTTTTTTTTCCCCC | 57626 |
rs201936363 | in-del | -/TAAT | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722265 | ACCAAATATTGTTGA[-/TAAT]TAATAATAAAATAGT | 57626 |
rs201940869 | in-del | -/TG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075554 | ACATATATATATACC[-/TG]TGTGTGTGTATGTGT | 57626 |
rs201950833 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789339 | ATAAATTAAAAATAT[-/A]AAAAAATCAAAATAT | 57626 |
rs201954603 | in-del | -/TAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780990 | ATCCCCAGATTATTT[-/TAG]TAAGTAAGTAAGTTT | 57626 |
rs201961605 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69911568 | TAGGAATATCATCAA[A/G]AAAAAAAAAAAAAAA | 57626 |
rs201964935 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70042932 | TATATATGAGACTGA[A/G]TCTCACTCTGTTGCC | 57626 |
rs201967870 | in-del | -/ATAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69840691 | ATTAACTTTATATAT[-/ATAA]ATATATATATGTATG | 57626 |
rs201977511 | snp | A/C/G | 1.65693e-05 | 0.00287826 | synonymous-codon, missense | KLHL1 | GRCh38.p7 | 13:69961396 | GGCTTCACAAACATC[A/C/G]CTTGTAAACATGGCC | 57626 |
rs201992609 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833444 | GGCTATTGTCAAAAA[-/AT]AAAAAAAAATAGATG | 57626 |
rs202007385 | in-del | -/TAC | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076911 | GGAACTGTAAATTAA[-/TAC]TACAATGATATACCA | 57626 |
rs202009184 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69717763 | GTCAGTCTATTAGCA[G/T]CATTTTTAAAATAAA | 57626 |
rs202011548 | in-del | -/TG | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822955 | TTATGTTTTTATAAC[-/TG]AACTTATTTTGCTCA | 57626 |
rs202018478 | in-del | -/TATA | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956149 | TATGATATATATATT[-/TATA]TATATTTGATATATA | 57626 |
rs202020812 | in-del | -/AGGA | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708443 | TTTGATTCCCTGGGT[-/AGGA]AGGTACTTTCAGTTT | 57626 |
rs202026266 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69903513 | CCCTTTCTTCGTTCT[A/C]GTTCTCTAGAAAGCA | 57626 |
rs202028254 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719207 | GTGTGTGTGTGTGTG[A/T]GTGAGAGAGAGAGAG | 57626 |
rs202047189 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69743261 | ATGTGATTGCTATGA[G/T]ATTTATTCTGGATGT | 57626 |
rs202054987 | in-del | -/TATTTAAAT | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963744 | GAAGAACATAAAATA[-/TATTTAAAT]TATTTAAATTTACTG | 57626 |
rs202063847 | in-del | -/T | 0.030278 | 0.119257 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822922 | ACATGTGCAATTCAG[-/T]TTTTTCAAAAATATA | 57626 |
rs202068411 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69890239 | GCAATAACAATTTCC[A/C]AAAAAAGAAAATGTT | 57626 |
rs202069685 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70004518 | GTTTTATCCTGCCAT[-/C]CCCCCTGACTAGTCC | 57626 |
rs202072348 | in-del | -/TCTATCTATCTATCTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789018 | TGGACTCCACAGGAC[-/TCTATCTATCTATCTA]TCTATCTATCTATCT | 57626 |
rs202074563 | in-del | -/TCTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789065 | CTATCTATCTATCTA[-/TCTA]CTTATTTACCTACAT | 57626 |
rs202079407 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020785 | TTTGTCTTCATATTG[A/T]GAGATATATATGTAT | 57626 |
rs202083508 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69948095 | TTAGAGATTGTTTTC[-/A]AAAAAAAAATGAAAT | 57626 |
rs202084023 | in-del | -/G | 0.329783 | 0.236927 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828233 | ATGTGAGAGGGGAAA[-/G]TCAGCCTCCAAGTAC | 57626 |
rs202086917 | in-del | -/TTTTTT | 0.409891 | 0.192184 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039057 | TATATCCTTTGCACA[-/TTTTTT]TTTTTTTTTTTTTGT | 57626 |
rs202093327 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70018670 | TTAAAGGCACATGTG[-/A]ATAATCCAAAGAGAT | 57626 |
rs202097726 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901905 | CGGGTTCAAGCGATT[C/G]TCCTGCCTCAGCCTT | 57626 |
rs202109762 | in-del | -/A | 0.0146672 | 0.084371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729768 | AACTCAATTTAAAGG[-/A]AAAAAAATCAAGTAA | 57626 |
rs202111759 | in-del | -/TATGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855911 | GTTTTATATATATTA[-/TATGT]TATAACATATTAATA | 57626 |
rs202112685 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976488 | AATATAGACTGTTTC[-/A]AAAAAAATAACTTTA | 57626 |
rs202122111 | in-del | -/TTTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69925687 | AAATAAACTCTAACA[-/TTTG]AAGTTTTATTGCCTT | 57626 |
rs202136111 | in-del | -/AAAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69810642 | TAGAAAAACAAGAAC[-/AAAC]TAAACAAAGCTAGCA | 57626 |
rs202143927 | in-del | -/CT/TG | 0.211212 | 0.246973 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736689 | GTGAGATATATATAT[-/CT/TG]GTATATATATATACA | 57626 |
rs202145323 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001618 | CTATCTATCTATCTA[C/T]CTATCATCTTTCTAC | 57626 |
rs202154745 | in-del | -/G | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870446 | TCAACATGAGTTTTT[-/G]GGGGGACAAACATCC | 57626 |
rs202161620 | in-del | -/A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69743793 | TTGTCTCAAAAAAAA[-/A/C]CACCAAAAAACAAAA | 57626 |
rs202169334 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69964056 | GTCAGTTTGTTTGTT[G/T]TTTTAAAAATAGGCT | 57626 |
rs202172692 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804297 | ATGTAGACAAATATA[-/T]ATTTTTTTGTGGGGG | 57626 |
rs202182045 | in-del | -/A | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843116 | AGAAGGATTAAATTC[-/A]AATGTATGATAGCAG | 57626 |
rs202184877 | in-del | -/TC | 0.02016 | 0.0983543 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819834 | ATTTTATTATTATTT[-/TC]TCTGTTTTGGCTCCA | 57626 |
rs202185345 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69968555 | TTTAAAAAAAAAAAA[A/G]AAATTGAAGGTATTA | 57626 |
rs202188791 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69958318 | TGAAAAACCTGATCT[C/T]ATTGCTTCTCATCTA | 57626 |
rs202198030 | in-del | -/AGATAGATAGATAGATAGACAGAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855330 | GATAGATAGATAGAT[-/AGATAGATAGATAGATAGACAGAC]AGATAGATACATAGA | 57626 |
rs202215315 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020803 | GATATATATGTATAT[A/G]CATACATACACATAC | 57626 |
rs202226850 | in-del | -/ATAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69753838 | ATGGCATAGAAATAA[-/ATAA]TTGAAAAAAAAAATT | 57626 |
rs202240606 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69791334 | AGATTGGAAGATTTA[-/T]TTTTTTTTTACGTGG | 57626 |
rs207474005 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69809429 | AAAGCAAAGAAATGC[A/C]AGCCAAGAATTTCAT | 57626 |
rs207474006 | snp | A/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824885 | ACTTAAGATTTGCAC[A/G/T]TCTCAATGAATGTAA | 57626 |
rs207474007 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69899478 | TAAGTAGGGCCCCTT[A/T]CAAGAAATTTGTGAA | 57626 |
rs207474008 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69990513 | AGAAAAAAGCAGGAG[A/C]TGTAATCCTAATTTC | 57626 |
rs207474009 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70047239 | AAACTTGGTTTGACC[A/T]GCTTGATTTAAAAAA | 57626 |
rs367555621 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69731199 | AACACAAATGAACAT[A/G]ATTTTTCTATGAATG | 57626 |
rs367568253 | in-del | -/TAGATAGA | 0.233527 | 0.249457 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855289 | CACTCGTACTAATTT[-/TAGATAGA]TAGATAGATAGATAG | 57626 |
rs367571243 | in-del | -/CA/CACA | 0.453635 | 0.159014 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975810 | TGACAGCCTATAAAC[-/CA/CACA]CACACACACACACAC | 57626 |
rs367614126 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69782557 | GCCCACAGAGTCTCA[C/T]TGATTGCTAGCATAG | 57626 |
rs367638450 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055018 | AAGTTTATTCAAAGA[C/G]GTAATAGAAATCTTT | 57626 |
rs367641149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738461 | TTCACTGAGCTAAAG[C/G]GTTATGTCCTAACTC | 57626 |
rs367652094 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70006044 | GCCACTGGCAACCAC[C/T]ATTTCATTCTTCGCT | 57626 |
rs367654775 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094951 | GTAGAATAAATACCA[A/G]TGGCTATCTTCTATA | 57626 |
rs367656078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703874 | ATCTGGGTTGGTCTA[A/C]GTATACTTTGTAATA | 57626 |
rs367674796 | in-del | -/TC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69944977 | TTAAACTATAAAACT[-/TC]TTTTTTTTTTTTTTT | 57626 |
rs367678894 | in-del | -/AAAC | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050119 | AGATGACACTATAAA[-/AAAC]AAACAGCCTCTAATT | 57626 |
rs367679077 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70064416 | GATGACGTGAAATGA[C/T]CTTTTCAGAAGTGAA | 57626 |
rs367681998 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69790959 | TCAGCCTGATAAAAA[A/C]ATCTATTTTTAAAAA | 57626 |
rs367687430 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084907 | AAACAAGATCTAAAA[C/T]GCGGAATTTTGAAGC | 57626 |
rs367690164 | snp | A/G/T | 0.000571078 | 0.0168887 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838931 | TAAAAGCTGCAACAC[A/G/T]GTATAACACAGGATG | 57626 |
rs367690375 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70025697 | CTATATATATTATAT[A/G]TAGTATACATATGAT | 57626 |
rs367696033 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69814152 | AATAGGGAAAGAATA[A/C]CCTAATCAATAAATG | 57626 |
rs367700741 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69798429 | TAAAGGTAATAGCAA[C/T]AATTAGATATGTCAA | 57626 |
rs367712872 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70054171 | GCTAGTCACATAGAT[G/T]GTCTCATTTTCATTT | 57626 |
rs367715987 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69986598 | CATTCTGCTGCTTGT[C/T]TTATTCTTATGGAGT | 57626 |
rs367716841 | in-del | -/ACAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833857 | TACACACACATATAT[-/ACAC]ACACACACACACACA | 57626 |
rs367720786 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70009698 | TCAATTTTTTCATCT[C/G]TAATGTGGAACTAAT | 57626 |
rs367723857 | in-del | -/GGCTTAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69771355 | ATTATATTTAAAGTT[-/GGCTTAA]GGCTTAAGCAATAAG | 57626 |
rs367731765 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981598 | CAGGCAATGTATATG[A/T]CTTTAGATTATATTT | 57626 |
rs367745650 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936746 | ACAGCCATTGAAAAA[A/C]CTATGAAGGTCAGGG | 57626 |
rs367751428 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69926712 | CAGCACTTTGGGAGG[C/G]TGAGGCGGGTGGATC | 57626 |
rs367754537 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69859200 | ACTGGTGTATCTGCT[C/T]CCATTCTTCTTTTTA | 57626 |
rs367757017 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70013629 | AACAAAATGAATTAT[-/AT]GTTTCCTTAGAATTG | 57626 |
rs367761053 | in-del | -/AAGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789886 | CAACATTAAGTAAGT[-/AAGT]TTGGAGGAGAATGTA | 57626 |
rs367774551 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69927713 | GAAATACTATTTTAC[A/G]CATACTAGGATGGCT | 57626 |
rs367779049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082186 | ACAGCCTGCAGAAAT[C/G]TGAGCCAATTGAACA | 57626 |
rs367792706 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70103983 | GATAAAATGACTGCA[C/T]TCTGTAAGAATTCAG | 57626 |
rs367795039 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69871418 | GGATCCCCTTTAGTC[A/G]CGCTAATTTCTCTAG | 57626 |
rs367843589 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833749 | TAAAGAAATAATGGT[-/A]TATATATATATATAT | 57626 |
rs367856386 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70103138 | CGTTTATGCATGACA[A/T]CTCTGTGATGAATAG | 57626 |
rs367857665 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69758975 | CCCTAATGTTCCCCC[-/C]AGGGTGTTCTGGGTC | 57626 |
rs367857936 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721082 | ATATATATATATAAA[G/T]CTATGTACCTCCCTT | 57626 |
rs367861566 | in-del | -/AA | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055807 | CCTCAAATAAAAAAT[-/AA]GTTACCGCAAGTGCA | 57626 |
rs367879809 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026645 | AGGCCCAGAGTTTTG[A/C]AATGGCTAGAAATTC | 57626 |
rs367894401 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804418 | CCTCACTTATCTTGC[A/G]TACAGCACAGAATTC | 57626 |
rs367897312 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69771215 | TTGCAGACTTTTGTT[A/C]TGTGTTGCCTGTTCT | 57626 |
rs367901235 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754874 | GAACCTCAGCTTATC[G/T]GATGAAATTCCACTG | 57626 |
rs367906494 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69739341 | ATGAAGCTACTACAT[A/T]GACAAGTCTGCAAAA | 57626 |
rs367906859 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69842811 | CAATGGGTTAATGAA[C/T]AAAGAAAATGTGGTA | 57626 |
rs367906891 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70018423 | ATTCAGCAGCTGTTC[C/T]AGCAGTACACACCAA | 57626 |
rs367914081 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70014400 | TGGCTATACAATTCA[C/T]TGTTGTTTGTTTAAA | 57626 |
rs367928813 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020637 | ACCTTTTATCTATGA[C/T]TCCCAGGGCACAGAT | 57626 |
rs367929072 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982557 | ACTGAAAGAGAGAAC[A/G/T]AAAGTAAGAAAGAAT | 57626 |
rs367932120 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69935277 | CTACTGGTGAACTTG[G/T]TACATAGCAGTCAAT | 57626 |
rs367933242 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69866274 | ATTTCCAGGTCTTTT[A/C]AGGTCGGCTTATTGA | 57626 |
rs367934233 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778313 | CTCAGATCAAATGAT[A/G]TATGTCTCAAGGTTT | 57626 |
rs367941599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917371 | AAATGTACAAAAGTA[A/G]GAAACTCCATATTAC | 57626 |
rs367945848 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69734856 | CATTTCTTTCTCATG[C/T]TCAAGAAAATACACT | 57626 |
rs367949267 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981037 | GAATTTATATCCCAA[A/C]ACCTAACAGAATGCC | 57626 |
rs367953050 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69854860 | AACGAGAATTCCAAG[A/G]AAATTCTTAATTGTA | 57626 |
rs367962070 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107236 | CCTGTTGCCTGGCTA[C/G]AGTTGTCTGGCTCCA | 57626 |
rs367977794 | snp | A/G | 6.66656e-05 | 0.00577307 | missense | KLHL1 | GRCh38.p7 | 13:69839032 | ACTGTAGATTTTCTG[A/G]GTTTAGTTCTCGGAC | 57626 |
rs367983913 | snp | A/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69815725 | TTTTTTAAAAAAGCC[A/G/T]TAAATGAACTGGAAT | 57626 |
rs367987367 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69972188 | TATTTATATATGTTG[G/T]TTAGGTAAGTAATTT | 57626 |
rs367988886 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69762180 | ACTTACTTCCCTAGA[C/T]AAGTTGTAAAATCTG | 57626 |
rs367999150 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69891207 | TAGATACAACTCTGC[C/T]GGACTGAAGTGAATG | 57626 |
rs368070042 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69740677 | AAATGAAAAAAAATT[-/A]AAAAATTGAATAGAT | 57626 |
rs368079197 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720126 | TAGCTAAAAACAAGA[C/G]TTTACAGGAAAAAAG | 57626 |
rs368081076 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69909715 | TTTAAGATATGGCTG[G/T]GTGAAGATAATACAC | 57626 |
rs368095586 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099115 | GGAATTTTACTTACA[C/G]TATTCTCTCTGATAT | 57626 |
rs368102625 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69987700 | ACACTAAAGATTTGT[A/T]TTGGCTCTCTTTGAA | 57626 |
rs368106124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827658 | TCTCGTGAACCCCAG[A/G]AGTCAGAGGTTTCAG | 57626 |
rs368108452 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70037101 | TAATCACTGTTGATT[G/T]TTGTAATGCCAATTT | 57626 |
rs368123767 | in-del | -/TGAT | 0.434398 | 0.168811 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783697 | GACCAAATCTACGTC[-/TGAT]TGATTGGTGTACCTG | 57626 |
rs368128075 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69876869 | GTGGCAAAACCCCGT[C/T]TCTATTAAAAATACA | 57626 |
rs368145981 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69932320 | ATTTTTTTCTCATTA[A/T]AAAAAGCAAATTATT | 57626 |
rs368168135 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69795312 | GGATTGATGGTGGAG[C/T]AGACATGAATGCAAA | 57626 |
rs368173809 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70058350 | CCTCCACCAAAAAAA[-/A]AGCTATTATAATTGA | 57626 |
rs368174615 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69886527 | TTTGAAATTTTATTA[A/G]AAATATAAATTTTTA | 57626 |
rs368181631 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936580 | GGTGACAGACAGAAC[A/G]AGACTCCATCTCAAA | 57626 |
rs368189499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956238 | ATAACAAAAAGTTGT[A/T]TTTAGTGCTAAATTT | 57626 |
rs368197036 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971586 | AAAATAGTATGCCAT[A/G]TCTTTTCCACTAGGC | 57626 |
rs368199100 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70000095 | GAGGCTGGCACCTCT[C/T]TCTCTGTCTCCTGCT | 57626 |
rs368215721 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69917953 | ATGTCTACATATCTG[C/T]ATTCATACATGTACT | 57626 |
rs368222505 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715780 | TCATGCAGCTGACTC[C/T]AGCAATAATATATCG | 57626 |
rs368230043 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69817924 | ATGATGAGGTTCAAA[A/G]CCCTCTATTAAGAGG | 57626 |
rs368233080 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948989 | TGACATTTTTAGTAA[A/C]TCATAGGTATTTTAA | 57626 |
rs368234176 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69708679 | AATATTTTATATTTT[A/G]AGTAGCAAAACCCTG | 57626 |
rs368248582 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732822 | CCAGCAGATTGGCAT[A/C]TTCTTCTCAGAGCAC | 57626 |
rs368248607 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70082194 | CAGAAATGTGAGCCA[A/G]TTGAACATCTTTTCT | 57626 |
rs368249913 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69718871 | AGCTCCAATCAGTCT[C/G]TCTTATGTTAAAAAT | 57626 |
rs368251877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090297 | TTCTGAGGCTCCAAA[A/G]AGTAAAATTACTGAA | 57626 |
rs368253828 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70067849 | ATCCAATAATATGAC[A/G]ACCAGTGGAGCAAAA | 57626 |
rs368260964 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819630 | GCAAAAAAAAAAAAA[-/A]TGTAGAAATAAAAGA | 57626 |
rs368264590 | in-del | -/ATATATATATAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69939341 | TATACATATACATAC[-/ATATATATATAT]ATATATATATATATA | 57626 |
rs368319446 | snp | C/G | 4.95446e-05 | 0.00497693 | synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107424 | AAGCAGGGTGCCATT[C/G]AGCGGATTGAAGGAA | 57626 |
rs368333240 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70056350 | ATAAACAAATATTAT[C/T]AGAGCTAAAGAAAGA | 57626 |
rs368337194 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69834424 | GTCCTATGGGAAGAG[C/T]TGTGTCGGTAACAGC | 57626 |
rs368338222 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69960728 | AACATTCAACAAATG[C/T]TTGCTATAATGGCAA | 57626 |
rs368344935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818431 | TCACCATGTTGGTCA[A/G]GCTGGTCTCCATCTC | 57626 |
rs368347013 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70034306 | AAAGTACTCTACTAT[C/T]GAATGTGATTTGAAA | 57626 |
rs368355193 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69870366 | CACCCAGACATTCAT[A/G]AGGGATCTACCCCAC | 57626 |
rs368357229 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028354 | AATTCAGTATATATA[G/T]AGACAGAGGTATGTC | 57626 |
rs368369212 | snp | G/T | 3.29473e-05 | 0.00405864 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69796916 | CATCATCCCTGCCTG[G/T]ATCCACAGATTTGTT | 57626 |
rs368393505 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045183 | TATGGTTTTTCTAAG[-/A]AAAAAATAGATTACT | 57626 |
rs368399930 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69862932 | CAGTCTATAAGATTT[C/T]ATGTAAGCTGAAGCA | 57626 |
rs368407948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939707 | TGGAGGGTTATGTGC[C/T]CAGGGAGGGCCTGGA | 57626 |
rs368410575 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099846 | TTTTATATGGCAGAA[C/T]AGTATTTCATTATAT | 57626 |
rs368415362 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70052182 | TTTGTTAATCAGAAC[C/T]GGAATTCAAAATTAA | 57626 |
rs368426198 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69794119 | GCTACCAGCTCTAAG[A/G]TTAAGGCATCCACAG | 57626 |
rs368432947 | in-del | -/AACTT | 0.000579832 | 0.017017 | intron-variant | KLHL1 | GRCh38.p7 | 13:69701783 | AAAAAGATGAAACAC[-/AACTT]AAGACAAGTTTTCAT | 57626 |
rs368433416 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69910883 | AAGCAATCAGGAAAT[A/C]AGCAATGAATTTGTT | 57626 |
rs368441928 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70023257 | TATTATCAAATTTTT[C/G]TTGCATATGTTTTAT | 57626 |
rs368453056 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69998194 | TTCCAAAGCAAGAGA[A/G]GCCTCTGCTTTAGGT | 57626 |
rs368453341 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027910 | GGCGATGTTACACAG[C/T]GGCAAAGGATTTGGT | 57626 |
rs368465379 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69774968 | TTGAACAGAGGCTTC[A/G]TGTCTTGTGGAAGGG | 57626 |
rs368482659 | in-del | -/TCT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70009161 | TAAGTCACGACTCCT[-/TCT]ATTAATAAGTCTTAT | 57626 |
rs368497811 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777140 | CAGTTTCCCTGCACA[C/T]GCTCTCTTGTCTGCC | 57626 |
rs368503085 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69716881 | ATAGATGACATCTTC[C/T]GGACCTAATTTCTCC | 57626 |
rs368508598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851243 | TTGCAAGAAGATAAT[C/T]AGAAAAGGATATATT | 57626 |
rs368565577 | in-del | -/GG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721102 | GTACCTCCCTTACAA[-/GG]AATTTCCTTGTGGAC | 57626 |
rs368566838 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69703981 | TGTTCACAAGCCCTA[C/T]CACTAAATGGAAATG | 57626 |
rs368577961 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870683 | GGTTATGCAAGCATC[A/G]GGTAAACATTCCCAT | 57626 |
rs368580912 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807075 | GTTTTGCCTTTGGCC[-/T]GAGTTCAGGCTGACA | 57626 |
rs368583201 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762615 | AAGGGCTGCTCCAGA[C/T]TCTTGGAACTGTGCA | 57626 |
rs368584848 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947029 | ATTGTGTGTGTGTGT[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 57626 |
rs368605327 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885937 | GAAATGGAGACATAT[A/C]GTATTCTGGCCAGTG | 57626 |
rs368606455 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69958178 | TTTAAGAAACTTCTT[G/T]TGAACTGTTATCACC | 57626 |
rs368670609 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70025326 | TCTCAGTGGTGATCT[C/G]ATTTAGTTGACTTTG | 57626 |
rs368679105 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70046230 | GTGAGAAAAAAAAAA[-/A]TGTCATAAAGAGGAA | 57626 |
rs368688223 | in-del | -/CTGTGTGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70042285 | TGTGTGTCTGTGTGT[-/CTGTGTGT]GCGTGCTTGTGTGGG | 57626 |
rs368690033 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69939391 | TATACACACACACAC[A/G]CACACACATACAGGG | 57626 |
rs368690366 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69733548 | AGAAATAGAAACAGA[A/G]AAAATTTTGAAAATA | 57626 |
rs368705615 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69899479 | AAGTAGGGCCCCTTA[A/C]AAGAAATTTGTGAAA | 57626 |
rs368708602 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70081489 | TGCTGCAGGACTGAG[A/G]TCCTCATTTTGCTGT | 57626 |
rs368715380 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70047895 | GTCTTGGTGCTTTTA[A/G]GTGCTCAGTTTTAAA | 57626 |
rs368723525 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69788555 | TTAGGAGATATGCCT[A/G]ATGCTAAATGATGAG | 57626 |
rs368746639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079526 | CTAAAAATAAATAGC[A/G]GTAATGCCTTTTCTT | 57626 |
rs368748328 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69818867 | AGGGCAGTACTCAAA[G/T]GGGCAAATATGAAAA | 57626 |
rs368758643 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69814778 | AGCAATTTGGGAGGC[C/T]AAGGCAGGTGGATCA | 57626 |
rs368758697 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084622 | TGCCACCACGCCAGG[C/T]TTTTTTTTTTTTTTT | 57626 |
rs368761116 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69709661 | ATTAAAAAATAAAGT[C/T]ATTATTTTTGTTTGT | 57626 |
rs368780616 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69969872 | AAAGAAGTATATGCA[C/G/T]GCAACCACACTAGAA | 57626 |
rs368785659 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902079 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC | 57626 |
rs368788851 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69854198 | ATTATAAAGAAAAGA[A/G]GTTTATTTGGCTCAT | 57626 |
rs368792660 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69739921 | GGGGCATCTAGTGGG[C/T]AGAAACCCAGGACAC | 57626 |
rs368803373 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69864401 | AATGTATACTATATA[C/T]ACATATAAATATACA | 57626 |
rs368812513 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69886718 | AGCAGCTAATATCAA[A/G]CCAACACATTATGTA | 57626 |
rs368822869 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69990881 | CACACGGTACATGCT[C/T]TAAAGTCAACCATGC | 57626 |
rs368848157 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69705400 | CTCAAGCTAAACTGA[A/G]TTTTTTTCCAAATAT | 57626 |
rs368920906 | in-del | -/AAGA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69860749 | TACAAATTCTATTTA[-/AAGA]AGATGAACAATAATA | 57626 |
rs368924182 | snp | C/G | 0.000117427 | 0.00766159 | utr-variant-5-prime, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107708 | CTGACATGCTTTACG[C/G]ACAGAAGGCAAAAGG | 57626 |
rs368924239 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69779380 | TTCCTCCCCTCCCCT[C/T]TCCTCCCCTGTCCTC | 57626 |
rs368927674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944397 | TTTCATTTGGCCTTC[A/G]CCCCATAGGTAGTTT | 57626 |
rs368933442 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936532 | AGGCGGAGGTTGCAG[-/T]GAGTGGAGATTACGC | 57626 |
rs368934043 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70088025 | ATCACCATGGCACAT[A/G]TTTATCTATGTAATA | 57626 |
rs368941745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905344 | TTAAAAATTGTATGT[C/T]AATAAGAGCACCATG | 57626 |
rs368942018 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69978263 | AAAGGATAATTAAGT[A/C]AGGATTTGTAGGCTG | 57626 |
rs368944568 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70085818 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 57626 |
rs368965266 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70013536 | AAATACCTCATGAAG[C/T]TGAAGCATTGTTCTT | 57626 |
rs368966278 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69807596 | TATAATCCCACACCC[A/G]GCACCATTCTGAGTG | 57626 |
rs368966841 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70057638 | AAAATTAGCCGGGTG[C/T]GGTGGCGGGCGCCTG | 57626 |
rs368971872 | in-del | -/CAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69708781 | GTTCAGATACAAAAA[-/CAA]AAAGGGTGGTAAGAA | 57626 |
rs368975059 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69891970 | ATTTAACAAAACTAA[C/T]AAATTTCTCAAATAT | 57626 |
rs368988533 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | KLHL1 | GRCh38.p7 | 13:69882322 | TATAAAGGCAAGAAG[C/T]ATGCTCAGGTCATTG | 57626 |
rs368988584 | snp | C/T | 6.45168e-05 | 0.00567928 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796687 | TTTATCATATAGTTA[C/T]ATTATCAATAACATG | 57626 |
rs368996330 | in-del | -/AACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781247 | CTTTGAATCCTAACA[-/AACA]CTAGAATATGCTTCT | 57626 |
rs368996810 | snp | A/C | 1.64955e-05 | 0.00287184 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975590 | TTAAACATGTGAATG[A/C]ATGTTTCCAGTAGAG | 57626 |
rs369047420 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084604 | GCTGGGACTACAGGC[A/G]CCTGCCACCACGCCA | 57626 |
rs369066787 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995062 | AGCCCAGTTAAGCCA[G/T]TCGCCTTTTAAGGAT | 57626 |
rs369073020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982017 | GGGAGAGAATAAAGC[A/G]TACTGTGTTTTTGCT | 57626 |
rs369076094 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69740228 | GCAATTTTGGGTTCC[A/G]TTGTCTATAGAGAGA | 57626 |
rs369082293 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723888 | TGCTTTTTTGCCCAG[A/G]CTGGAATGCAGTGAT | 57626 |
rs369084206 | in-del | -/GTGTGTGTGTGTGTGAGAGA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719196 | TACGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGAGAGA]GAGAGAGAGAGAGAG | 57626 |
rs369091860 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69785968 | CCAGGAAGAAGTTGA[A/C]TCTCTGAATAGACCA | 57626 |
rs369095382 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985883 | CCACTGTGTGTGTGT[A/G]TATGTATATAAGTAT | 57626 |
rs369096082 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69823416 | GGTTGTTGGTGAGGC[A/G]TTAGGCTCTAAAGTC | 57626 |
rs369096318 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921690 | TCATTCATTTGTTTA[G/T]TCAATCAAAACAATA | 57626 |
rs369097139 | snp | A/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70042585 | CAAACATACTGCACC[A/G/T]CCAGCTCTATAAAAA | 57626 |
rs369099782 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780733 | ATATATATATATATA[C/T]ATATATATATACATA | 57626 |
rs369113134 | in-del | -/TTAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69888004 | TGCTATAAAACCATC[-/TTAG]TTAGACTGGATAATT | 57626 |
rs369116124 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69745946 | CAACATTGTCTCTTC[C/T]AATCCAGAACACAGT | 57626 |
rs369117556 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804308 | TATAATTTTTTTGTG[-/T]GGGGGGGGAAATAGT | 57626 |
rs369124098 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799872 | GGTGAGCGGCACCCC[A/G/T]AGCTCCACCTTCTGT | 57626 |
rs369131293 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995984 | ACTGCATTCATAAGC[A/T]CTTTTCAGATATCAG | 57626 |
rs369132531 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068296 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 57626 |
rs369139534 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70054726 | AGTGACTGCAATATT[-/A]AAAAAAAAAAAATCA | 57626 |
rs369141428 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69877705 | TAAATAACTGAATTT[C/G]TTTCTGGATTAGTTA | 57626 |
rs369171195 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69826334 | TCATGCCTGTAATCC[C/T]GGCACTTTGGGAGGC | 57626 |
rs369181327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780611 | CTGTCTATTCATTAC[C/T]CATTGTTATATATAT | 57626 |
rs369193484 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69973149 | ACCTTATCTACTTAA[A/G]AATATGCCTAACAGT | 57626 |
rs369194586 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69799932 | GGAGCGCAAACCCTA[C/T]TGTGAACTGTGCATG | 57626 |
rs369245729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994206 | ACAGTGATATACAAC[A/G]TAATGCCTGTTTACT | 57626 |
rs369258503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038281 | TTCTGTGGTAGCAAT[A/G]TACTATGGCTTTTTA | 57626 |
rs369266029 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70029107 | TTTCACTTTTTGTCA[A/C]CATTCTGTGTTGAGT | 57626 |
rs369266520 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69818823 | GGAACCAAAGTGACT[C/G]AATGTAGTCACTGAG | 57626 |
rs369267982 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850964 | TTTCTAAATAGCGTT[G/T]GAAGGTTATCTTTAT | 57626 |
rs369274213 | in-del | -/GAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780188 | TGTATGTGATTTGAG[-/GAG]TATGTGGATACAAGC | 57626 |
rs369279590 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69756286 | TACAGAAAGGGATAA[C/T]ACTAGTGCAAAATAT | 57626 |
rs369288070 | in-del | -/TTC | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021652 | AGCAATGAATGAGAA[-/TTC]TTCTTCTTCCACGTC | 57626 |
rs369293828 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69744534 | AAATACATATTAAAT[C/T]ACATTGTATATGTAA | 57626 |
rs369294059 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70083561 | AACTCTGTGCAAATC[A/G]TAATATTGTGAAGAT | 57626 |
rs369305165 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69889781 | GCATCCATGATAATG[A/C]ATTCTTATCAGAATT | 57626 |
rs369336148 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086618 | AAAGAAAGAAAGAAA[A/G]AAAGAAAGAAAGAAA | 57626 |
rs369345644 | in-del | -/CACACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70082312 | CCTCCTTGGACCTGT[-/CACACA]CACACACACACACAC | 57626 |
rs369346362 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084175 | ATGAGGAAGGTACTT[A/T]AAATTATACACACAC | 57626 |
rs369349006 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70049754 | AAAATGAGGCCAAGA[C/T]AAACAATGCGGTGTT | 57626 |
rs369357309 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69960300 | AAATGCTGTAAAAAA[A/T]AAAACTCCTTAAACT | 57626 |
rs369359076 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69764741 | CCTCTCAACACAGAT[C/T]GACTCAATTCTATTC | 57626 |
rs369362791 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961759 | TTCACCATGCTAACT[A/T]TCCCCCCTAAACTAT | 57626 |
rs369365315 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70007051 | GTTCAGAGAAAACAA[C/T]CGGATTGAAATTATG | 57626 |
rs369370134 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69791664 | ATTTTTGACAAGGGT[G/T]CCAAGAATTCAGTGG | 57626 |
rs369388836 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820518 | AAAAAATAAAAAGGA[A/T]AATTGAAAAAGGGAA | 57626 |
rs369390670 | in-del | -/ACC | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025824 | GCCCTACATACGTAA[-/ACC]ACCTCTGATCATCTT | 57626 |
rs369397664 | snp | C/G | 3.84076e-05 | 0.00438205 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796712 | AACATGTTTCTAAAA[C/G]TAATATCAATAAAGT | 57626 |
rs369423658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906074 | GCTAAGTGGCTTCAC[A/G]TTGGGAATTTTCAGT | 57626 |
rs369428652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809742 | TCGATTTAAAAGACA[C/T]AGAGAGGTAAATTGG | 57626 |
rs369432000 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69871232 | CCTTTAAACCACAGC[G/T]GGAGCAGCCTGGATA | 57626 |
rs369438864 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69929191 | AACTTCATTGCTTCA[A/C]AGTTAATGATAAACA | 57626 |
rs369441244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878636 | TATATGTAACATTAC[A/G]TGTGTGTATATAAAC | 57626 |
rs369445051 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69828861 | GTAACTCCATTGGCC[A/G]GAGAACCACACCTCC | 57626 |
rs369467077 | in-del | -/GAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69953281 | CCTCAGGCTACTCAT[-/GAT]TTGATGTACAACAAT | 57626 |
rs369471818 | in-del | -/TA/TATATATATATATA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70094393 | CAATGCAATCATCTT[-/TA/TATATATATATATA]TATATATATATATAT | 57626 |
rs369477774 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70018500 | AAGATTAGTACCTGA[C/T]TTAGAGACTGATGCA | 57626 |
rs369485462 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949972 | TCTTCTAAAAATTAC[C/T]GCAAAATGATTTTAG | 57626 |
rs369490102 | in-del | -/TTTAT | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850975 | CGTTTGAAGGTTATC[-/TTTAT]TTTATCTATAAACAA | 57626 |
rs369497105 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734435 | ATGAACTAACACAGT[A/T]ATAAAGAAAAATAAA | 57626 |
rs369523518 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69988219 | TGTGTGGTGGTGTTT[C/G]GTTTTCTCCTCCTGC | 57626 |
rs369535714 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70103008 | TTCATATATGGTTAC[A/G]AGCTTCAATAAGAAT | 57626 |
rs369539602 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013334 | AAATACCAATGGTAA[C/T]GATATATTACATGGC | 57626 |
rs369549636 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69848632 | CCATGGCTGTCACTT[C/T]AAAATGAAAACACAA | 57626 |
rs369556287 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70061436 | TGGAGTCACTTCCAA[C/T]ACATAAACAGTATAT | 57626 |
rs369565632 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69989327 | TATGCGTCTCTTTTT[A/G]TACTAGTATCATGTT | 57626 |
rs369573714 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69877845 | ATATCCTCTGTTATA[A/T]TTTCTACACCAAATT | 57626 |
rs369575567 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998744 | GTTCTCTGATGGCTT[C/G]GGTTGTCTGGTCATC | 57626 |
rs369575688 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69743263 | GTGATTGCTATGACA[A/T]TTATTCTGGATGTTT | 57626 |
rs369578534 | in-del | -/AGTAAGA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69968325 | GTATCATGTAAATAG[-/AGTAAGA]AACTGATATATTTGC | 57626 |
rs369578540 | snp | G/T | 3.38409e-05 | 0.00411331 | missense | KLHL1 | GRCh38.p7 | 13:69701707 | TATCAATAAGTCAAG[G/T]TTGCTTGATGACTAC | 57626 |
rs369606491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811178 | AACAGTAACAACAAC[A/G]AAACTACAGGCTAAT | 57626 |
rs369606937 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69941734 | AGCTTAACCAAAAAA[-/A]GAAGAGAGAAGATCC | 57626 |
rs369616149 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69803408 | CCACTCTGAGAAACA[C/T]TTCTTTTTATGACTT | 57626 |
rs369631774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836378 | AAATCCAGGCAGAAA[A/T]TGGAAGCTAAGATGT | 57626 |
rs369640831 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69857236 | AAAAACTCTCCTTCC[G/T]GAGTCCCTGACAAAC | 57626 |
rs369649022 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897461 | CTTTATTGAAAAACT[A/G]TATAGAACACTTAGA | 57626 |
rs369649080 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69871947 | TTCCAATCTTTGCCC[A/G]TTACCCAGTGCCAAG | 57626 |
rs369651994 | in-del | -/GAAGAAGAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69933005 | AAAACAAAAACAGAG[-/GAAGAAGAG]AAATTTCCTTTGTAC | 57626 |
rs369706080 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70099002 | TTTTGTAACTTTTAG[A/C]TTCTTACTCAAAAAA | 57626 |
rs369711468 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70037465 | TCTGTCTTTGATATT[C/T]TGTTATATACCCGGC | 57626 |
rs369714745 | in-del | -/TT/TTT | 0.457737 | 0.139088 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960110 | TCAGAGCATGTGTAC[-/TT/TTT]TTTTTTTTTTTTTTT | 57626 |
rs369715300 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110050 | TTGCAGTTCCTTTTT[C/T]TCTGCAATACTAATA | 57626 |
rs369717175 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893335 | CGCTTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 57626 |
rs369720894 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985210 | TGTGGGAGAAAATAT[C/T]TGCAAACTATGCATC | 57626 |
rs369724710 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69967372 | AAGGGTTTAAGACAT[C/T]AGTGGAGGAAGTAAC | 57626 |
rs369730675 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70096021 | TGTTGCAATTAACAT[A/G]ATTTCATTCGTTTTT | 57626 |
rs369731907 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038110 | ACTTGTTTTCCATCT[A/T]CACGTTTAAGCCATT | 57626 |
rs369733589 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075561 | ATATACCTGTGTGTG[-/TA]TGTATGTGTATATAT | 57626 |
rs369748214 | snp | A/C | 0.000232454 | 0.0107784 | missense | KLHL1 | GRCh38.p7 | 13:69839057 | TCGGACTTTGCATTA[A/C]AGTTCTTCTTTCTGG | 57626 |
rs369748220 | in-del | -/AC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780757 | TACATATATATATAT[-/AC]ACACACACATTTATA | 57626 |
rs369751886 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69810575 | CTGAACATCTACATC[A/G]AGAAGATAGAAATAT | 57626 |
rs369763303 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730295 | TGTGTGTGTGTGTGT[-/G]TGTTTTCATTACAAA | 57626 |
rs369780063 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795791 | TCTCTCTAGTTCCTG[G/T]TTACCCCATAGCAGG | 57626 |
rs369788427 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69892140 | TGAACATCGGTATTT[A/G]CCAATATTCTTTAGG | 57626 |
rs369794607 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69796063 | TTCAACTGTACATAT[C/T]GTATGATCTTTGAGG | 57626 |
rs369795560 | in-del | -/CTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70024686 | TGTCTCTTTTTCTTT[-/CTTT]ATTTCTCTTTCAGTT | 57626 |
rs369805380 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69926140 | AACTTTAATCATCAC[A/C]GCTGTTCGGTTTGAT | 57626 |
rs369805737 | in-del | -/AGTAAGTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70064390 | CCTCACCATAAATAT[-/AGTAAGTT]GGGGATGACGTGAAA | 57626 |
rs369807005 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69967230 | CATCTGGCAAAGTAA[A/G]TTTAAAACTTTCTGG | 57626 |
rs369821000 | in-del | -/GT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060555 | AAAAAAAAAAATGTG[-/GT]GTATATATAGGCCAG | 57626 |
rs369830875 | snp | A/G | 6.63967e-05 | 0.00576142 | intron-variant, synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975790 | TGTCATTGAATGGCC[A/G]GTTGATGACAGCCTA | 57626 |
rs369848337 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69725981 | TCATCTCTCAGTCAG[C/T]TGAGGTTGTGTCTCC | 57626 |
rs369856496 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885768 | GCCCTGATAATCATC[A/G]TGAGGACAAAATGGA | 57626 |
rs369870871 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933393 | CACTCCAAATATTCT[G/T]CTAAGGCAAACTCTA | 57626 |
rs369879549 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961194 | CTACTAGTTTTCAAC[A/T]GAAAAGATACAGAAT | 57626 |
rs369884053 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70071884 | AAAATTAATAATCTA[C/T]TCTTCAGCCCCCCAA | 57626 |
rs369888306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898881 | CCTGGAGACTCACCA[C/T]TGATTATAAGTGGTC | 57626 |
rs369893940 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70058111 | CACAGAGCCATATAT[A/G]ACAGTCCCACAGGTA | 57626 |
rs369901424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943464 | AGGTTGGAAAATACA[A/G]TGATTAGAGTAATAT | 57626 |
rs369910714 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69952926 | ATCTCTACCAAATTT[C/T]AAATGGAAGATATTA | 57626 |
rs369921324 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730880 | CCACTGTGCCTGGAC[A/G]GAGAACATTCATTCT | 57626 |
rs369923217 | snp | G/T | 6.69042e-05 | 0.00578339 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961460 | CTGAAAGAGTCACAG[G/T]TTCTAATTTAGGTCG | 57626 |
rs369936693 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780727 | ATATGTATATATATA[C/T]ATATACATATATATA | 57626 |
rs369941459 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69809290 | GCAAAAGAAAAAAAT[A/G]TTGAAGGCAACTAAG | 57626 |
rs369943089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765130 | CTAATTATTATTTTT[C/T]GAGTAGAGATGGGAT | 57626 |
rs369943425 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781166 | CTGACTATGTCTCCC[A/G]TAATGTCAAGAACTC | 57626 |
rs369947506 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70058297 | TCAAATTATCCTTGT[G/T]TGCAGATAATATGAT | 57626 |
rs369948303 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050924 | CTCATATTTGTCATA[C/G]CTAATTGGAGCAGAT | 57626 |
rs369955860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785282 | TCATCAAATGTAAAA[G/T]AATAGAAATTATAAC | 57626 |
rs369972517 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70004633 | AAATATGTACAAAGA[C/T]TTTACATGACATATT | 57626 |
rs369980651 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007209 | GAATGTGTCGTATTG[C/T]AATAAATCAAATGTG | 57626 |
rs369986393 | snp | C/T | 0.00177145 | 0.0297083 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740578 | TATTAGATAAATGAA[C/T]GTAGTGCCTATAGTT | 57626 |
rs369987972 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69944950 | AATGGATCACGAAGC[A/T]AAATTCAAACATTAA | 57626 |
rs369988803 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739610 | AATCCTAGTTTCTGA[A/C]AAAATAGACTTTAAA | 57626 |
rs369996004 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979853 | TTTGATCTCTTGAAC[C/T]CCTCAAACCATAGCT | 57626 |
rs369997464 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69735270 | TCAAATAACAACTGA[C/T]ATCAGAGACTATAAA | 57626 |
rs370020135 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824245 | AGGTTGTTACACAAC[A/G]TATGAAATGTTATTA | 57626 |
rs370050952 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69914455 | CTTTCTCTTGATACA[A/C]AAGGAATAATCCAGG | 57626 |
rs370054913 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022280 | TGATTACGTGTGTGT[-/G]TTGTGTGTGTGTGTG | 57626 |
rs370059581 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081380 | TACACTGCTGCAATC[A/C]AGATTTTGGGTCCAC | 57626 |
rs370061491 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804859 | TTTTAAAAAGCAGGA[A/G]ATAGTGAGATGCATT | 57626 |
rs370067588 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947130 | GTGTTTCCATCACCC[C/G]TTGTGAACATTCTGA | 57626 |
rs370072567 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885743 | AGGTTTATCAAAACC[C/G]TGATATATGGCCCTG | 57626 |
rs370074989 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69874127 | ATATAGTACTCATAC[A/G]AATAACAAAAATAAT | 57626 |
rs370090600 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770019 | AGCCAGAGCTGTGAC[A/G]TGCCCTTGTTCACTG | 57626 |
rs370103127 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69954395 | GAACACTTGGAAAAA[C/T]GGTGATTGAATTCAA | 57626 |
rs370114665 | in-del | -/TCAGAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70003310 | GAAAATGTAAAAGAG[-/TCAGAG]AAAAGTGGATACTTT | 57626 |
rs370115479 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70059223 | GAGTGCAGTGGCACA[A/G]CCTTGGCTTACTGCA | 57626 |
rs370119439 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014844 | TTCTAGAAAATGTTA[C/T]GTTAGCTCACTTTTC | 57626 |
rs370122669 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089502 | TCAAATACACACCTC[C/T]AGATTGTTAAAATAG | 57626 |
rs370138516 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70090017 | CTCCTCTGAAAAGCC[-/C]ATTTAATCAATAGTA | 57626 |
rs370144565 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69722931 | CTAAATGCTCAACAA[C/T]GGATAAATGGATAAT | 57626 |
rs370145961 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064688 | ACAATACATATATTC[G/T]GAAAAAAATACAGAA | 57626 |
rs370150664 | in-del | -/TAAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69723479 | AACAAAAAAAGAAAG[-/TAAG]CCCAGGACCAGATGA | 57626 |
rs370156722 | in-del | -/GTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70040946 | CTTTTCTCTCTGTTT[-/GTTT]TACAGATTGGGTGAC | 57626 |
rs370163239 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69890908 | TCTTATATATACAAA[C/T]ATATACTTGTTTAAT | 57626 |
rs370170445 | in-del | -/TACAGCCTCCTGCCC | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872313 | GCAATCGGCCTGTTT[-/TACAGCCTCCTGCCC]TACAGCCTCCTGTAG | 57626 |
rs370185462 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69935257 | GAACTTGGTACATAG[C/T]TCACCTACTGGTGAA | 57626 |
rs370200015 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69743792 | TTTGTCTCAAAAAAA[-/A]ACACCAAAAAACAAA | 57626 |
rs370210096 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70059393 | CAGGCTGGTCTCAAA[C/T]TCCTGACCTCAAGTG | 57626 |
rs370221619 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69731881 | CACAAGTAGTAAATA[A/G]AAAAACAAAGTAAAA | 57626 |
rs370226161 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69921074 | ATGACCAAATAACAA[G/T]GGACAACTATTTTTT | 57626 |
rs370231509 | in-del | -/GAAGAAGAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69983598 | AAAAAAAAAGAAGAA[-/GAAGAAGAG]AAAAAAAAAAAAAAG | 57626 |
rs370255346 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996896 | TTATGAAAAGTTCTT[A/T]TTTTATTCATTAAAT | 57626 |
rs370256918 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786387 | AATCCAGCATATAAA[C/T]GGAACCAAAGACAAA | 57626 |
rs370258081 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69842737 | GGATACTTGCATTCA[C/T]ATGTTTATTGCAGCA | 57626 |
rs370258431 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69988173 | TCTGTCCATGTTCTC[A/G]CATTACTTAGCTGCT | 57626 |
rs370264804 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978767 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT | 57626 |
rs370273605 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69900540 | TACCCACACCTTTAG[G/T]ATTTGTTGAGCAAGA | 57626 |
rs370274187 | in-del | -/TCA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100181 | ATGAATATTATATAT[-/TCA]TATTTCTTCATTATG | 57626 |
rs370282045 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69904170 | TAATAATAGAAAAAT[A/G]AAATGCATTAAGTTT | 57626 |
rs370282721 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70082147 | TTGTAAGTCTCCTGA[C/G]AGCTCCCTGGCCATG | 57626 |
rs370318542 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102191 | TGTCCCACTAATCTC[C/G/T]ATGAGATTTTTAATG | 57626 |
rs370325059 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70070180 | GAAGCAGAAGAAATA[A/G]TTATAGTAATAATTA | 57626 |
rs370330278 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69713744 | ATAACATATAACTTT[A/C]TAAAAAACATATAAA | 57626 |
rs370381929 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69758511 | CAAAAATCACATCTT[C/T]ATGCCTTTTAAAATA | 57626 |
rs370382168 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69774725 | TCTGTTCAATTGTAA[C/T]AAAATAATGCAATAA | 57626 |
rs370382433 | snp | A/C | 0.000316184 | 0.0125695 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69961438 | GGAGACTGAACTCAG[A/C]ACAAGCCTGAAAGAG | 57626 |
rs370389769 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973542 | TACATTTTGCTTAAA[G/T]ACAATATTTAGTTGT | 57626 |
rs370396776 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69862679 | AGCCTTTAAGGAGAC[A/C]ATTAATACTAAATGA | 57626 |
rs370401669 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70097268 | TTGCTATATCAAGAA[C/T]AGATTTTAAAATAAA | 57626 |
rs370404147 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69920373 | TCCATTTGTGGTTCA[C/T]AGTGCTATTTTAAGA | 57626 |
rs370411297 | snp | A/G | 0.126909 | 0.217598 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786808 | AGCAACTTCAGCAAA[A/G]TCTCAGGATACAAAA | 57626 |
rs370414397 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748592 | TGGGGTCACAGAGCC[A/T]GACCATATCACCACC | 57626 |
rs370416822 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69861399 | CAATATGTTTATCAG[C/T]TTTTAAAATAGCATC | 57626 |
rs370425247 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69748433 | AGCGGAATCCCCTGA[C/T]AAAACCATCAGATGT | 57626 |
rs370438969 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69930795 | ACTAAGGCCATTATA[G/T]AATTCATTCCTTAAA | 57626 |
rs370439807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808115 | CAGGAATGGATATGG[A/G]AAGCGGGTCACCTCT | 57626 |
rs370448289 | in-del | -/AAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69958238 | TCTTACCAGTTACCA[-/AAT]AATAATAATAATAAT | 57626 |
rs370450760 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69703363 | AAAGAAAAAAAATTA[G/T]ACAGCTGGACAATGT | 57626 |
rs370454240 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70101489 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTTAC | 57626 |
rs370455531 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70062557 | TAACAAACCTGCACA[G/T]TCTGCACATGTACCC | 57626 |
rs370467155 | in-del | -/AAAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70043416 | TTATTGAAGAAAGAA[-/AAAT]AAATAAATTTAGTGT | 57626 |
rs370467930 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70002793 | TATAAAAAGCAAAAC[C/T]ATTAACAAGTAGAAG | 57626 |
rs370468042 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69849171 | ATAGGTCTCGAATAA[A/C]ATCATTTTCACTCAC | 57626 |
rs370469260 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69767455 | TAATCCCAGCACTTT[C/T]GGAGGCTGAGGTGGG | 57626 |
rs370473018 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834001 | GGAAAACCTAAAATC[A/G]TATGTTCTCATTTAT | 57626 |
rs370474317 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084810 | AGCCACTTCAAACCA[C/T]GATTAAAATTCTAAA | 57626 |
rs370485580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793823 | GAGAGCCTGACATCA[C/T]TTGTGACGTTCTGAG | 57626 |
rs370493752 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855505 | TAATCCCCATAATTT[C/T]CACATATCAAGGGAG | 57626 |
rs370506366 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022603 | TTTGTTTTTAAATTT[C/T]TACTATTTACATGAT | 57626 |
rs370512333 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69967444 | GTGGAATCTGAAGAT[A/G]TAACTGAATTGCCGC | 57626 |
rs370519362 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884585 | TATAGTGAGGGATGT[C/G]ATAAAAAACAGCTCT | 57626 |
rs370526691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708458 | AGGAAGGTACTTTCA[A/G]TTTATTCAATAGAAA | 57626 |
rs370550470 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69707676 | CATAGTGTTGAGGTA[C/T]GTCTGTCCATCATAG | 57626 |
rs370551689 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69966093 | TTCCAACCTAACAGA[A/G]GCTGCAGCTTCTGTG | 57626 |
rs370569607 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69746280 | CTTTCAATATAATTA[C/T]TATACATTTTAGTTC | 57626 |
rs370575504 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69810544 | AAAAGCAAGGTTAAC[A/G]ACAAAGTTTATAGTG | 57626 |
rs370582482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804077 | ACAGTATAGTTCTTT[A/C]AAATGTGCATTTTTA | 57626 |
rs370599960 | snp | C/T | 2.01278e-05 | 0.0031723 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939998 | TTTTACCTCTGATAA[C/T]ACAGAGTGTGTCTCC | 57626 |
rs370601351 | in-del | -/AATAA | 0.0577627 | 0.159827 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109546 | AAAGTTGGACGCTTT[-/AATAA]AATAAGAAATTAAGT | 57626 |
rs370644626 | snp | A/C/T | 8.781e-05 | 0.00662557 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107576 | CAAAGCTGCCACTGC[A/C/T]GTCCTGTTGCAGGCA | 57626 |
rs370650889 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69718480 | AATGAGGAAAAAAAG[A/C]ATCATGGTATTAAAC | 57626 |
rs370678112 | in-del | -/TGTGTGTGTGTGTA | 0.188316 | 0.242271 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022292 | GTGTTTGTGTGTGTG[-/TGTGTGTGTGTGTA]TGTGTTTGGTTGTAG | 57626 |
rs370705523 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70014914 | GTTGCACACTATGTT[A/G]AACCATTTTAAAACA | 57626 |
rs370706923 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70012536 | AAGAGGGGGAGGGGG[A/G]CTTGAAGATGCTATT | 57626 |
rs370709701 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69980978 | TTCCATACACCACAC[A/G]GATGTGTTGCTCAGA | 57626 |
rs370711932 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69716415 | GCACCTAGTTTAGTG[-/A]AAAAAAAAATGATGT | 57626 |
rs370716666 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063179 | TCCAGCTCTGATTAC[C/T]TCTCTAAGTAGACTA | 57626 |
rs370719483 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060851 | AACTTCGTCTCAAAA[A/G]AAAAAAAAAATGTGG | 57626 |
rs370725519 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69870214 | TGCTGCCACTCGTAG[C/T]GGAAGTTTAAGGGGA | 57626 |
rs370732209 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870624 | TACAGCTGTGATCCT[A/G]CAAAATAAAAATATA | 57626 |
rs370749274 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69920760 | TTCCATTCACAATTG[C/G]TCTTAAGAAAAATAA | 57626 |
rs370817640 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69822835 | AAAGATTAAATTGAT[A/C]TTGATATTAAAATTT | 57626 |
rs370831784 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69875118 | GATCAAATCAACTGT[G/T]TCAAACACAATTGAG | 57626 |
rs370835005 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855335 | ATAGATAGATAGATA[C/G]ATAGATAGATAGACA | 57626 |
rs370838054 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70098967 | CTTTATACTTAGTCA[A/G]TATTTAATAAATTTA | 57626 |
rs370840575 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69728170 | TGAGTCTAAGATTAA[C/T]TAAAATGTATACAAT | 57626 |
rs370843016 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69790481 | ATACCTAAACCAGAC[A/G]GAGACATGATAACTA | 57626 |
rs370850106 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69791345 | ATTTATTTTTTTTTA[C/T]GTGGCAATACTCACA | 57626 |
rs370873520 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70044876 | GTCAGCACACCAGGA[A/G]TTATAGAACTGAACT | 57626 |
rs370885482 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69915801 | TACCATCAGAGTGAA[A/C]AGGCAACCTACAAAA | 57626 |
rs370922340 | snp | A/G | | | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970243 | AACTGCTCATCACAT[A/G]TCCCAGGACATTTCA | 57626 |
rs370923451 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69727061 | TTAATTATGTGTCTC[A/G]GGAACACAAAAGTAG | 57626 |
rs370931197 | snp | A/G | 5.0974e-05 | 0.00504821 | missense | KLHL1 | GRCh38.p7 | 13:69940198 | GGCACGCTGCAGCAA[A/G]AAGGTTCTCAATGGT | 57626 |
rs370971557 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69876992 | CAGTGAGCCAAGACT[-/G]TGCCACTGCACTCCA | 57626 |
rs371007383 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69979243 | CATTAAGTTTCTTCA[-/T]ATTGTATCTGAGAAC | 57626 |
rs371011630 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69777275 | ATTATCCATTCTCAG[A/G]TATTTCTTCATAGCA | 57626 |
rs371038688 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69754160 | AATTAATATTCTGAA[G/T]GTACTTCAGTAGGAG | 57626 |
rs371054554 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70015111 | ACAAACACACACATA[C/T]ACACATATGGTCATG | 57626 |
rs371061658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910659 | ATGCTTTATCAGACA[A/G]AAAATTCATATAAAA | 57626 |
rs371072035 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076711 | TGTAAAGCCACAGAC[C/G]AGGAGAAAATTTTTA | 57626 |
rs371081798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011837 | GTCCATTTTCATGCC[A/G]TTGATAAAGACATAC | 57626 |
rs371084817 | snp | C/T | 0.39009 | 0.207062 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783693 | AAAAGACCAAATCTA[C/T]GTCTGATTGATTGGT | 57626 |
rs371093873 | snp | A/C | 0.000255187 | 0.0112928 | utr-variant-5-prime, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107721 | CGCACAGAAGGCAAA[A/C]GGCTGGCAGCTCACG | 57626 |
rs371111689 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020108 | TGTGAGAAATAAATT[C/T]CTGTTCTTTATAAAT | 57626 |
rs371122104 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70043152 | TCTGGTGATCCACCT[-/G]CTTGGCTTCCGAAAA | 57626 |
rs371143547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043946 | TGCAATTGTTCCCTA[C/T]TGGTGTCTTCACTGC | 57626 |
rs371193036 | snp | A/T | | | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970833 | AAATCCATCATGAAA[A/T]CCTGAATTCCAGGCT | 57626 |
rs371193465 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69784249 | CAAAATGTAAAGACC[A/G]TCAAGGCTAGGAAGA | 57626 |
rs371196286 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69938493 | ATAGTCCAAGCAGCT[G/T]CAAGGAAAATATTTT | 57626 |
rs371198759 | snp | A/T | 3.34007e-05 | 0.00408647 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797005 | CCAATTGCTATAAAT[A/T]CAACAAACAGCCTGC | 57626 |
rs371210758 | snp | A/G | 4.06793e-05 | 0.00450977 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838926 | CAATATAAAAGCTGC[A/G]ACACGGTATAACACA | 57626 |
rs371210873 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69773410 | AGTTAGAAGAGAATA[C/G]AACTTCCTATATTTT | 57626 |
rs371211762 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086610 | AAAGAAAGAAAGAAA[A/G]AAAGAAAGAAAGAAA | 57626 |
rs371215596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830628 | GAGAACATTCTACCC[A/G]ACAGCTGCAGAATAT | 57626 |
rs371224160 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753851 | TAATTGAAAAAAAAA[A/T]TTTTGAGACCAGTCT | 57626 |
rs371226509 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69872076 | GCTAGATAATTTATA[-/TA]ATGAAAACAAGTTCA | 57626 |
rs371240569 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70018303 | AAGATAAAATAAATT[C/G]TCCAATGTCATAAAA | 57626 |
rs371245953 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69889416 | TACTCATGGTCAAGA[C/T]AAGGCTAGGATTAGA | 57626 |
rs371250928 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70006938 | ATTTTTCATTTTGTT[C/T]TTATATCAAAATACA | 57626 |
rs371251075 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918431 | GCATAAACTTTTATA[A/G/T]GCACTGTTTATTTTT | 57626 |
rs371251481 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804420 | TCACTTATCTTGCAT[A/G]CAGCACAGAATTCAG | 57626 |
rs371253084 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69989111 | TTACATTTAAGTCTA[C/T]AATCTGTCTTGAAAT | 57626 |
rs371259644 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69830156 | CCACATAAAAAATAC[A/G]GAATGGATAATAATT | 57626 |
rs371270216 | snp | A/T | 0.000153988 | 0.00877328 | missense | KLHL1 | GRCh38.p7 | 13:69796833 | AATGTCTTTAAGCCA[A/T]CTCGACCTCCAATTA | 57626 |
rs371288682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888102 | TGTTGTTTGGCGAGG[A/G]CTCCTTCCTTACAGA | 57626 |
rs371311178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877365 | TAAAATGTTAAAACA[C/T]GTTATTTATTTTATA | 57626 |
rs371324942 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69955702 | AAATATAGTGAACCT[C/T]AGTGCATCCTTTCCA | 57626 |
rs371335028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846751 | CAAAATAGTCACATG[C/T]TTAGCAACATTAAAG | 57626 |
rs371345848 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812688 | ATTTCTGAAAAGAAG[A/G]CATTTATGCAGCCAA | 57626 |
rs371352530 | multinucleotide-polymorphism | AC/GA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068418 | GTGACACTGATTAAT[AC/GA]ATTATGATTTTATTA | 57626 |
rs371369965 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69740272 | TTTGTCAATTTAAAA[A/G]TATCAACAGCTTAAA | 57626 |
rs371371713 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70008420 | TCTATGAACATATAA[A/G]TGTGTATGTATCTAT | 57626 |
rs371376494 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708790 | CAAAAACAAAAAGGG[A/T]GGTAAGAACCCAGAA | 57626 |
rs371380264 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69725611 | ACTCATTCATACTCT[A/G]TCAGGCTTCACAACC | 57626 |
rs371395133 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857555 | ACTCACAAGAATATG[C/T]ATTTCCCTAGAATGT | 57626 |
rs371403302 | snp | A/G | 5.4036e-05 | 0.00519761 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107159 | CGCGGTGAAATGAGT[A/G]GAAATTGAGAGATGC | 57626 |
rs371403748 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69709100 | ATGTGTAAAATGAGG[C/G/T]GCTGGTCGAATGCTA | 57626 |
rs371406717 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70095096 | GAAGAGTGATTGAAA[A/G]CACAATTTCTGCTCC | 57626 |
rs371413546 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69870355 | CATGAGGACAGCACC[A/C]AGACATTCATGAGGG | 57626 |
rs371414982 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719155 | GGAGGAAGCAAGGAA[C/T]AAAAGAATAAGAAAA | 57626 |
rs371419390 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69816394 | GCTTCCTGAGTAGCT[A/G]AGATTACAGGCATGT | 57626 |
rs371422921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078255 | CCACCTTCTTATTAC[A/G]ACATTCACAGTCAGA | 57626 |
rs371428011 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69711278 | GTGATTTATAGTCCA[G/T]TAGGTTTGCCTGTAA | 57626 |
rs371432432 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810336 | TTTTAATTATATGAA[A/G]CATCTCCTTGGATCA | 57626 |
rs371433977 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69821703 | ATCTGATTTAACTTA[C/T]CAAAGTGGCCTTCCG | 57626 |
rs371437182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767417 | AGAAATATCAGTTAT[C/T]CAGGCATGGTAACTC | 57626 |
rs371451951 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69942200 | CATATTTTTTGCCTG[A/T]GTAAAGCATACATTG | 57626 |
rs371460869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788750 | ATAATATTAAGCAAT[A/G]AATACTTGGAGCTCC | 57626 |
rs371468812 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70104149 | AAAAATATATGGTTA[C/T]CTGAATATCCAGGAA | 57626 |
rs371475822 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69979397 | TCCTCAACCTTATAC[C/T]TAATATAGAATTTTA | 57626 |
rs371484132 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69838165 | GTGATTGAAATAAGT[A/T]TTTTTTTTGTTCTGA | 57626 |
rs371484937 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69723859 | TTTTTTTTTTTTTTT[C/T]TGAGACGGAGTCTTG | 57626 |
rs371488613 | in-del | -/A | 0.112631 | 0.208878 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000937 | TACAGAAAAAAAAAC[-/A]AAAAAATAGATGCCA | 57626 |
rs371490801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805347 | ATTTTGCTTGCTATT[A/G]AACTAATCTCATTGA | 57626 |
rs371496116 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916484 | TCTCAGCAAACTATC[A/G]CAAGGACAAAAAACC | 57626 |
rs371525448 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69909717 | TAAGATATGGCTGTG[G/T]GAAGATAATACACAA | 57626 |
rs371531805 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020964 | TGTACGTATAGCCTC[C/G]CCTATTATCAACATC | 57626 |
rs371534416 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70097922 | AATAGGCTAGGTATC[A/T]TTGTGAAAAATATTG | 57626 |
rs371545024 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69992856 | AAATTAGTGAAGAAA[A/G]GCATATAGTCAATAT | 57626 |
rs371549671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017509 | GCTCTGATCAGTGGC[C/T]GGACCCAACAGTCAC | 57626 |
rs371552263 | snp | C/G | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107294 | TTTCGTGTGGTCCAG[C/G]AAAGTCCATGCCTGG | 57626 |
rs371560894 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69988366 | ATCCAGCCTATGGTT[G/T]TTTGGCATTTAGGTT | 57626 |
rs371588822 | in-del | -/AC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833856 | TACACACACATATAT[-/AC]ACACACACACACACA | 57626 |
rs371592451 | multinucleotide-polymorphism | AA/CC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69822121 | GGAGAATCGCTTGAA[AA/CC]CTGGAGGCGGAGGTT | 57626 |
rs371595674 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69912323 | AGTACATTTATCCCT[C/T]CTGATATAATGGATT | 57626 |
rs371599305 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69861809 | AAAAAAAAAAAAAAA[-/T]ACAAAATTAGCCAGG | 57626 |
rs371607481 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69889303 | TGTTGAACACTACCT[C/T]AGAATTTCAAAGGGA | 57626 |
rs371618403 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938761 | AAAGAAGGATTTGCC[-/A]ATAGAATTACAAATT | 57626 |
rs371621902 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70031115 | AATAGCCTGCCAACC[-/A]AAAAAAAAACCCAGA | 57626 |
rs371623268 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69786088 | GAGGTACAAGGAGGA[A/G]CTGGTACCATTCCTT | 57626 |
rs371626818 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69866536 | TGCATTGGTCTTCAA[C/T]AGATTTTACTTGGAA | 57626 |
rs371627482 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70077356 | ATGAAATAAGCTGGT[C/T]CACAAAGGCTACATA | 57626 |
rs371641209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942540 | ATTTATTAAGAAAGT[C/T]CTTTATGCATAATAA | 57626 |
rs371653466 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69782454 | TGGAAAATCGGGTCA[C/G]TCCCACCCTAATACT | 57626 |
rs371654184 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70000443 | AACAAGAAAAAAAGC[A/G]TATATACATTAGTTA | 57626 |
rs371660821 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70087865 | AGGAAGTAGGATTAC[A/C]AATAGATGCTCTTTG | 57626 |
rs371663022 | in-del | -/TC | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799121 | AGGTTTACACAGATA[-/TC]TGTCTCTTGTGACTA | 57626 |
rs371664611 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752031 | GCTTCTTGTGCCTCA[G/T]TTTCTTATCTGCACA | 57626 |
rs371669100 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69725502 | TGCTGGAAAGTCTTG[C/T]CTTTATTTTAGATGG | 57626 |
rs371673776 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70028482 | CTGGATTAAAAGAGA[C/T]CCACGGCAATTCAAA | 57626 |
rs371676592 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107978 | GGACGCCAAAAGCTG[A/G]GAATCCTCGATGCCC | 57626 |
rs371685756 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70085537 | GCTATTTTTAATATT[G/T]GGACACCCTAAAATT | 57626 |
rs371694980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759186 | ACAGAGTACATGTTC[C/T]CAAGCCTCACCATGG | 57626 |
rs371698542 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69709668 | AATAAAGTCATTATT[A/T]TTGTTTGTTTCTGGA | 57626 |
rs371699285 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743608 | TGGCCAACAAGGCAA[A/C]AATCTCGTCTCTACT | 57626 |
rs371711410 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69903538 | AAAGCACTTTCTTTT[A/T]TACCAGAGGGGCTGT | 57626 |
rs371728355 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69897130 | AAAAATCAAACAATA[A/C]GACATTATTTAAGAA | 57626 |
rs371733281 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69761948 | TTAGTTTGTCAAACC[-/C]ATAATTGTTGAAAGA | 57626 |
rs371736865 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69717003 | CCATAAACTATTCTA[A/G]AGTCCTCATTCTCAT | 57626 |
rs371737040 | snp | G/T | | | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700298 | ATTCCATAGTTTTCA[G/T]TGTTTTTTTAATAAA | 57626 |
rs371737670 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023154 | TAACATTATCACCAG[A/G/T]TTTTCATTTAGAAAA | 57626 |
rs371740970 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70056150 | AAGCAATGGAAAAAA[-/G]ATATCCCATGGAAAT | 57626 |
rs371746886 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69739022 | GCCAGGTCACCTGTA[A/T]AGGGAAGCCCATCAG | 57626 |
rs371783643 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69899156 | CAAAATTTATTGGAT[A/G]TCTTTGAATTTTGAA | 57626 |
rs371789185 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936877 | ACAATGGTGTCAGCC[C/T]GCAACAGTGGGGTAA | 57626 |
rs371790819 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69953237 | AAGCATCAATGACAA[G/T]TCTCCATTTGGGTAT | 57626 |
rs371801553 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020282 | TATGCAAATATGGCA[C/T]AATATTTTCCAGAAT | 57626 |
rs371804751 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69933807 | AAGGGGGAAAAAAAA[-/A]TACTTGAGAAAAAAA | 57626 |
rs371813416 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69796448 | GTTAAAAAGAGCCTG[A/G]CACCTGCTCCTGTCT | 57626 |
rs371819774 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749649 | AGAACACATAACTAT[A/T]TCCAATGAAGATGTT | 57626 |
rs371830103 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870574 | GTTCCAGCCTCAACT[C/G]AAAAGTCAAGCCTCA | 57626 |
rs371832127 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896102 | TTCTTGGTGGCCGTT[A/G]CCTGGAGGTCACTCA | 57626 |
rs371835393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770552 | CTATGTTGCTTAGTC[C/T]GGTCTTGGGCTCCTG | 57626 |
rs371860515 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69803020 | ATTCTCCATTCCCAC[G/T]GCTTCTCTCGACCAG | 57626 |
rs371864477 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69953883 | AAACTTATAAAATCA[C/T]ACATTATGAATAATC | 57626 |
rs371876461 | snp | A/G | 3.29913e-05 | 0.00406135 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69719440 | TCCTACTGCATAAAG[A/G]AAACCGTCACATGTG | 57626 |
rs371899150 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851323 | TTTTACAAAATTATT[A/T]CTGACTGGGCAACAC | 57626 |
rs371917786 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69950892 | ACAGAAGCAACAGTT[A/C]TATAATTCGTTGTTA | 57626 |
rs371918588 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69904529 | GCATCTTATTCCCAT[C/T]AGCCCTGGTACTATA | 57626 |
rs371959615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777158 | TCTCTTGTCTGCCAT[C/T]ATGTAAGACGTGCCT | 57626 |
rs371971091 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050791 | AGAGCAATTTTGCAA[-/T]ATTATTTGTCATATA | 57626 |
rs371972325 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69838608 | ATTCTCAACTTCTCA[A/G]AGACAGAGATTCTTT | 57626 |
rs371974371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739369 | AAATAACCAGACAGC[A/G]TTATGATGTCAGGAT | 57626 |
rs371984776 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69814393 | GCCAAAACAAAAATT[G/T]ACTATTGAGAGGTAA | 57626 |
rs371986979 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69866182 | ATTGCGGCAAATTGA[A/G]AAGTTGTTTAATGGT | 57626 |
rs371990686 | in-del | -/CAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70009817 | ATCCATAGTAATAAA[-/CAA]AAGACAAATTCCTAT | 57626 |
rs371995120 | in-del | -/AAAAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70012907 | ATTCTGTATAAAAAA[-/AAAAT]AATAATAATAATAAA | 57626 |
rs372032677 | snp | C/T | 0.000116491 | 0.00763098 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69839043 | TCTGGGTTTAGTTCT[C/T]GGACTTTGCATTAAA | 57626 |
rs372033299 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69850750 | TTTTAATTCCATGTA[-/C]TACAACTGAAAGTAT | 57626 |
rs372041820 | in-del | C/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69993689 | ATGGACTCCATTTTT[C/TT]TCATCTGGATGCCTT | 57626 |
rs372054900 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69850777 | GTATTTCCTAATGTA[A/G]CTTAAAGCACCTTGT | 57626 |
rs372054939 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084075 | AAAAGCAAAAACTAC[A/T]GTTAATATTAAAGTA | 57626 |
rs372056932 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885108 | ACCACGCCCGGCTAA[C/T]TTTTTGTATTTTTAG | 57626 |
rs372063337 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70006528 | TTTTTCAAAGAGTTT[G/T]AGAAGGATTTGTATT | 57626 |
rs372063493 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075617 | TATATATAGGACTTA[C/T]ATATATATATGTATA | 57626 |
rs372068172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912967 | CAACATGTGCTCCCA[A/G]TGTGGGGTCTCCTTT | 57626 |
rs372075675 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69823720 | ACACTACATGGATAC[C/T]GGGACTTTCTAAAAC | 57626 |
rs372075909 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69795498 | CAGATCTTTAAAAGA[A/C]AGTAATTTGTACTTC | 57626 |
rs372083797 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69946743 | GTCTAGAACTCCTGG[A/C]CCCAAGCCATCCTCT | 57626 |
rs372088670 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69744659 | TTCCCGAAAGGTACA[C/G]CCCCCCCAAAAGCTA | 57626 |
rs372091502 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721083 | TATATATATATAAAG[A/C]TATGTACCTCCCTTA | 57626 |
rs372121482 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69903166 | GTCATGTACTCTAAG[G/T]TCTCAGAAAGATGTG | 57626 |
rs372130838 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70017969 | AAACGTGAAAATAAG[C/T]GCTAATCTCCAATTA | 57626 |
rs372137324 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69924329 | TACTGTGCTTTTTCC[A/G]GGCCTGCCCATGGCT | 57626 |
rs372147094 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69972266 | TCAATTGTCACTTTA[A/G]CCTCAACTGTCTACA | 57626 |
rs372152680 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69951983 | CATTGAGTTATGTCA[C/T]AGATTATGTGACTGT | 57626 |
rs372170319 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69828689 | TGCTTATCAGCTGCC[-/T]GGATATAAACTCCAG | 57626 |
rs372171129 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69928527 | TAAACAACTCAAATG[C/G/T]CCATCAACCGATGAA | 57626 |
rs372189817 | snp | A/G | 0.000151084 | 0.00869018 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961475 | GTTCTAATTTAGGTC[A/G]TGAATGTAAGGCAGA | 57626 |
rs372193199 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855746 | ACCGTGAGTCAATTA[A/G]ACCTCTTTCCTTTAT | 57626 |
rs372198907 | snp | A/G | 6.60055e-05 | 0.00574442 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69719464 | ACATGTGGCCACTCC[A/G]ACACCCCCTCTCCTC | 57626 |
rs372221440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826519 | TGGGAGGCAGAGGTT[A/G]CAGTTAGCCAAGATC | 57626 |
rs372247453 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847936 | TATAAATATATCTAA[A/C/T]ACAAATAAAATAATT | 57626 |
rs372247543 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69918225 | ATAATTAAACTTTAA[C/T]AGTTTTGTAAATTTT | 57626 |
rs372280755 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085065 | AAAATCATATATCCG[C/T]ATGTGACCATAAATA | 57626 |
rs372305812 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70033426 | TCTCCAGTAGCTGGG[A/C]CTACAGGTGCCCACC | 57626 |
rs372310341 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026577 | TAACCCATTTGGGTC[C/T]GTTCCCTCATGAGTA | 57626 |
rs372318699 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70047964 | CCTTAGAACAAGACA[A/G]AACTATTTAAATAAG | 57626 |
rs372322167 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69940755 | TTTAGTTTTTTCTTT[G/T]TTTTTGTTTCCCTGT | 57626 |
rs372327126 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859440 | TGCAATATGTGGCTG[G/T]AGTGGTGTCTTTTCA | 57626 |
rs372330805 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936582 | TGACAGACAGAACGA[A/G]ACTCCATCTCAAAAA | 57626 |
rs372337122 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69934990 | TATATATATATATAT[A/G]TATATATATACATAT | 57626 |
rs372337199 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70040049 | ATGCCAACATTTCAC[C/T]AGTTGTAATGAAATG | 57626 |
rs372355233 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69813964 | AGCAAAAAGAATAAA[A/G]TTGGAGGCATCACAT | 57626 |
rs372372770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003028 | ATACCTAGATTTTAC[A/G]AAGCACTTTTAAAAA | 57626 |
rs372375859 | snp | A/G | 0.000164837 | 0.00907697 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107456 | AGGAGGAAGAGGACG[A/G]GGAGGACGATGAAGA | 57626 |
rs372441278 | snp | C/T | 3.29832e-05 | 0.00406085 | missense | KLHL1 | GRCh38.p7 | 13:69882434 | CTGGCCAGTAGTTTA[C/T]GGAGCTCCTCAGCTG | 57626 |
rs372449939 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838620 | TCAAAGACAGAGATT[A/C]TTTTCATAATTGAGA | 57626 |
rs372450116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984561 | CAATCTTTGGGCTCT[A/G]TGTAAATCAGATACT | 57626 |
rs372467598 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881521 | GTCACCTTCAAGCTT[A/G]TTTTTGGATAACTTT | 57626 |
rs372469101 | in-del | -/G | 0.0267878 | 0.112589 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911568 | TAGGAATATCATCAA[-/G]AAAAAAAAAAAAAAA | 57626 |
rs372471961 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69844777 | TTTTTTATTTATTTA[A/T]TTATTTATTAAGACA | 57626 |
rs372477161 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69925749 | AAGTTAATTTCAACA[C/T]TATTTTTTGTAGTGA | 57626 |
rs372483590 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69772963 | TTAAGAGGAATATTC[G/T]TGGATTCTTGAAAAG | 57626 |
rs372492826 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70082433 | TAAGGTCCAGGCTGG[A/G]GAAAGGGATCAAAAT | 57626 |
rs372495377 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70099935 | TAGCACTATCTTGAT[A/T]AATGTAGCTTCATAA | 57626 |
rs372498756 | in-del | -/TCAGTGCTAAGCCTATTA | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760160 | CTAAAACTACTACAT[-/TCAGTGCTAAGCCTATTA]AGGAGTAAGACAAAG | 57626 |
rs372501415 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70049079 | TACTAATAATAAATA[C/T]TTAAATGGCAATTTA | 57626 |
rs372508897 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70067999 | TTTTCAAATGTTTAT[C/T]TGATCACGGTAAATC | 57626 |
rs372515391 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69859957 | ACTCAATCTATCATC[C/T]GAAGGCCTAAACAAC | 57626 |
rs372521539 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013773 | TTGTTATCTCACAGA[A/T]GCCTCTGATACAGTC | 57626 |
rs372530792 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878022 | AAGTCAAGTTGGTCA[G/T]TTGCCTCATGAACAC | 57626 |
rs372537020 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928537 | AAATGTCCATCAACC[A/G]ATGAATGGATAAATA | 57626 |
rs372557296 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69987244 | AAATAAACCAGAATA[G/T]AGTGAAAAGGTAGTT | 57626 |
rs372564669 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69930551 | GAATCTCCTTCCAAA[A/G]AATACAAAACTATAT | 57626 |
rs372576560 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977388 | CAATAATTTAAGATT[C/T]TGATGTGCAAAATTA | 57626 |
rs372576721 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69727099 | AGAAAGATTAATTTT[A/C]ACTGGGTGGATTCAA | 57626 |
rs372595966 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69760512 | AGGCATGTACCACCA[A/C]ACCCGGCTAATTTTT | 57626 |
rs372604832 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69953683 | ATTACAAGCTAGTTG[C/T]TTAAAAAATTCACCA | 57626 |
rs372611521 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69746120 | CTATTTGTTTCATCA[A/G]TAAATAAAAAGAAAA | 57626 |
rs372615494 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961208 | CTGAAAAGATACAGA[A/G]TACAGAATTTTTTTT | 57626 |
rs372636475 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69864259 | GAATAATAGTCTGTG[C/T]TATTAAAGCACTCAT | 57626 |
rs372636983 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703215 | GCTGAAAAATTCCAT[C/T]GTCTGGTAATGTCAT | 57626 |
rs372642698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852244 | CTTCACACTCCATCC[A/G]GAATAGGTAATGGCC | 57626 |
rs372646811 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69934962 | GTGTGTGTGCATGTG[-/TA]TATATATATATATAT | 57626 |
rs372653146 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885797 | GATTTGAATAAAAAA[G/T]CTCGCCATATGGGAG | 57626 |
rs372655264 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70007959 | AATGCCACATTAGCT[C/T]ACATATAAGATTATA | 57626 |
rs372665893 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69768936 | CATCAATGATATTTT[A/G]CTTTCATGTAATGCA | 57626 |
rs372670015 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70002460 | AGCCTCAAAAGCATA[C/T]TGGAAAATATCAAGT | 57626 |
rs372673394 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70043274 | AATGAGAAAAGTTAT[A/G]TAATAAGAAAAAATA | 57626 |
rs372686181 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721105 | CCTCCCTTACAAGGA[-/AT]TTCCTTGTGGACAAA | 57626 |
rs372687996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821883 | ATGGCAGGGATTTTT[A/G]TAGTTTTGTTCACTA | 57626 |
rs372702754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104064 | TCACTATAAAATGCA[A/G]GAATATAAATATTGC | 57626 |
rs372706339 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69965383 | GTTACAATTGTTCTT[A/G]TTTGGCGGTGTCATA | 57626 |
rs372709604 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69873455 | ATCTGAGTGACAAGA[C/T]GGATATTATGTTTTG | 57626 |
rs372710123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957811 | GTGAAGAAAACCCAA[C/T]TGAAAGTCTTAAAAG | 57626 |
rs372730779 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69790705 | CAAAAATCACATGCA[A/T]ATTTCAATAGATACA | 57626 |
rs372777654 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69847590 | AAGAAAAAGTACTAA[C/T]TCTTCTAAAACTATA | 57626 |
rs372778828 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69795983 | GTTTCACTCAACCCA[A/C]ATTAACTATTTTTCC | 57626 |
rs372785157 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69876899 | AAAATTAGCCGTGCG[C/T]GGTGGCGCATGCATG | 57626 |
rs372808659 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780736 | TATATATATATACAT[A/G/T]TATATATACATATAT | 57626 |
rs372814294 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69948633 | CTGTTTTTCTATAAG[A/G]TATTTGAATTTATAC | 57626 |
rs372818672 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841624 | ATGATTTGAGCAATG[A/C/T]GGTCATTTTAATGAT | 57626 |
rs372843927 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69958672 | TTCTACAGCTAATAA[C/T]TAACTATCAATCATT | 57626 |
rs372845884 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70090857 | TTTAGTAAACCATAG[C/T]TATAGAAATTAAAAA | 57626 |
rs372847174 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70058990 | CAATAAATGGTGATG[A/G]GAAAACTGGATATTC | 57626 |
rs372870197 | in-del | -/T | 0.43309 | 0.17023 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979179 | GGCTCAAAAAAAAAA[-/T]AAATAAGTTCCAGTT | 57626 |
rs372872136 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69913923 | TCAGTGGACTGGGAA[-/A]GGCAGACCCACCCTC | 57626 |
rs372874364 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69726119 | TAAAGGATATTTCAA[A/G]GAAAGTGCACAGAAA | 57626 |
rs372886601 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69915495 | CGAGAAATGGGGAAA[C/T]GATTCCCTATTTAAT | 57626 |
rs372892716 | in-del | -/GGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69887333 | AGGCCACAGTGGCTG[-/GGT]TTTCCTCAGAGGGCA | 57626 |
rs372897707 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69874433 | TTCGACTATCTACTC[A/G]ATATCTCCACTTAAA | 57626 |
rs372904089 | snp | C/T | 0.000208807 | 0.0102157 | intron-variant | KLHL1 | GRCh38.p7 | 13:69701802 | TAAGACAAGTTTTCA[C/T]AGAAAAATATAAAAC | 57626 |
rs372930962 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944019 | AAAGAATGAGCACAG[C/T]AGACCTGAACTACTA | 57626 |
rs372947139 | in-del | -/TATC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69859950 | CAGAAAAACTCAATC[-/TATC]ATCTGAAGGCCTAAA | 57626 |
rs372947187 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708190 | CATTGTGGAATACTC[A/G]ACAGATGAAGTTTCC | 57626 |
rs372966159 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732068 | GTGATTGGAAGGAGG[A/G]GAGTCAAATAAAGAT | 57626 |
rs372980118 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69844058 | TTATATCAAATTTTA[C/T]AAATAATGGATAATT | 57626 |
rs372983049 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024533 | CAACGTAAGTTTTTT[C/G]TAGAATTGTCTTTTT | 57626 |
rs372986623 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780729 | ATGTATATATATATA[C/T]ATACATATATATATA | 57626 |
rs372987360 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093211 | GAAGAGAGAAAAGGG[C/G]AAGGCAATAAAGGCA | 57626 |
rs372988031 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69737782 | GCAGCTGTAGTATCA[C/T]GCATCAGTGGTCTCA | 57626 |
rs373000243 | in-del | -/GAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719072 | AAAGTATATCAAGAA[-/GAA]ATTTAAAGATTATTT | 57626 |
rs373009459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745814 | AATATCCTTTTGGTA[C/T]TTCATATGAATTTTT | 57626 |
rs373013887 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69723423 | AAGTATCAAAACATA[A/G]CATTATAACCCATGA | 57626 |
rs373014527 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985885 | ACTGTGTGTGTGTGT[A/G]TGTATATAAGTATAT | 57626 |
rs373016175 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70098089 | TGCAAGCATTTTCTA[C/T]CTAGTTTCATTAACT | 57626 |
rs373022124 | in-del | -/AGAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855410 | GATAGATAGAGATAC[-/AGAT]AGAGATAGAGACAGA | 57626 |
rs373046477 | in-del | -/GCACAAGAATA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69716338 | CAGAAATTGTACCAA[-/GCACAAGAATA]TAGAGATGGGTGGAA | 57626 |
rs373051225 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69900445 | TTAGAATTTACGGGT[A/G]AGGGAAACAAAATGT | 57626 |
rs373054069 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70016819 | GAGTCTGGGGCCTGG[A/G]GTGAGAACTTATGGT | 57626 |
rs373063186 | in-del | -/AG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69862295 | CACACACACAGGAGA[-/AG]AGAGAGAGAGAGAGA | 57626 |
rs373066164 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70010026 | AAAGTGCATTACAAG[-/A]AGGAGAAAAAAAAAA | 57626 |
rs373066223 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69987790 | CTATAATAATATGGG[C/T]AATATACACATAGAT | 57626 |
rs373069120 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827622 | GTAATCCCAGCTACT[C/G]GGGAGGCTGAGGTAG | 57626 |
rs373073963 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69809351 | CCTGGCAGACTAACA[A/G]CATATTTCTCAGCAG | 57626 |
rs373096566 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69888919 | GTTATTTCTTTTATA[A/G]AGTAATTCCCTTAAG | 57626 |
rs373121140 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885089 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 57626 |
rs373126607 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69856807 | CAAGTTATATTTCTT[C/T]TCTTTATCAAATTTG | 57626 |
rs373128526 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69752611 | GTTTTCTTTTAAAAC[A/C]AAAATCACAGTTGAG | 57626 |
rs373138388 | in-del | -/G | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821503 | ATTTTTAGTAGAAAT[-/G]GGGGTTTCATCATGT | 57626 |
rs373152793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778947 | GGGACTACAGGCACA[C/T]GCCACCATACCCAGA | 57626 |
rs373155700 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69783547 | GAAGCCTCAGGAGCC[A/G]ATGCGATCAACTGGA | 57626 |
rs373157182 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69803560 | GTCCATGAACGGCTA[C/T]GCTATATAGCATTGT | 57626 |
rs373167025 | in-del | -/GG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70024666 | TCTCTCTCTCGCTCT[-/GG]CTCTGTCTCTTTTTC | 57626 |
rs373178985 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69982592 | CAAACAACCAGAAAA[C/T]AATAAGCAAAATGGC | 57626 |
rs373193725 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70052866 | AGACATTTTGAATAT[C/T]ATCTTCTAAATAATT | 57626 |
rs373211861 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70032992 | CAATGGGATTGCTTT[C/T]TGACTATTAGCATTT | 57626 |
rs373239624 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69787198 | AAAGAGCCCTCATTG[C/T]CAAGTCAATCCTAAG | 57626 |
rs373254617 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69870220 | CACTCGTAGTGGAAG[G/T]TTAAGGGGAGCCAGC | 57626 |
rs373259180 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69967426 | AAAGAATTAGAATTA[C/G]AAGTGGAATCTGAAG | 57626 |
rs373261939 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867848 | CACACACTGGGGCCT[G/T]TTGTGGGGTGGGGGG | 57626 |
rs373280757 | snp | A/G | 1.65048e-05 | 0.00287265 | missense | KLHL1 | GRCh38.p7 | 13:69719391 | CATAATCCAGTAGCC[A/G]GGAACAGTGATTTGA | 57626 |
rs373281927 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69919546 | TGTACTTTGGGTACA[C/T]TAATGACACCAATTT | 57626 |
rs373282883 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086594 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAGAAA | 57626 |
rs373291087 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730064 | AAACTAGATAGACAA[C/T]TTAGTCATAACAACA | 57626 |
rs373300525 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70104803 | TGTCACAGAAAAAAA[A/T]TAAATCCACATTACT | 57626 |
rs373301947 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075358 | AAAAAATAAAAGCTA[A/T]AAAAATTGAAAAGGA | 57626 |
rs373315957 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715109 | AAATCACATAACTAA[A/C]TTGGTATAGCTATTG | 57626 |
rs373321199 | snp | C/T | 1.98908e-05 | 0.00315357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940005 | TCTGATAACACAGAG[C/T]GTGTCTCCATTATTA | 57626 |
rs373346792 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769454 | CAGACAGGGATGGGT[C/T]CCTGGTGAAACCCAA | 57626 |
rs373346968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017378 | CTCATCCAGACACAA[C/T]TGCCCACATCGGAAG | 57626 |
rs373361409 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69905404 | TTATAGTCTAAATTG[A/G]CCAAATGCTGGCATT | 57626 |
rs373392271 | snp | C/T | 1.70362e-05 | 0.00291853 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740589 | TGAATGTAGTGCCTA[C/T]AGTTAATATCATATT | 57626 |
rs373413034 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084755 | GCTGGAATTACAGGC[A/G]TGAGCCACTGCGCCG | 57626 |
rs373415280 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69786154 | CCTCCCTAACTCATT[G/T]TATGAGGCCAGCATC | 57626 |
rs373419050 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69954601 | TGGTAGATACATAAC[C/G]CTTACTCCTAAATAT | 57626 |
rs373423751 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107133 | TTAGACTTAGTAGCC[A/T]CATGAGCACACGCGG | 57626 |
rs373441004 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70014614 | ATATTATCATCCATG[C/T]ATGTATAATGAAAAT | 57626 |
rs373497577 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69963212 | GGACAGCATGCACAA[C/G]CACCTCACCTAGCAT | 57626 |
rs373498010 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69726598 | AATGAGGTTCTGAAG[A/C]CTGATAGGGTCTACC | 57626 |
rs373510727 | in-del | -/AGATAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69796236 | CCATAATTTACTTAA[-/AGATAA]TGATAATTGATGACA | 57626 |
rs373520404 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760202 | ACAAAGAAAGCATAC[C/T]CTCTGCCTAGACTCA | 57626 |
rs373536326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821396 | CTTGGCTCACTACAA[A/C]CTCCACCTCCCAGGT | 57626 |
rs373552191 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70004661 | ATTTTAAAGTTGTCT[G/T]ATAATTCTTAAAGGC | 57626 |
rs373561280 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69927698 | ACAAACAAAAACCAC[A/G]AAATACTATTTTACA | 57626 |
rs373564593 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69753010 | GTCTTCCTGAACTGG[A/T]GACTTTGCCTCTAGG | 57626 |
rs373570983 | snp | C/T | | | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701017 | TAAGCCTAGTGAAAA[C/T]AATCCTTTGTGTTTG | 57626 |
rs373574667 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69842316 | GAGGACAAATACGCA[G/T]AATGTACAGGAAACA | 57626 |
rs373576386 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69991774 | TCCAAAAAATTGAGG[C/T]GGAGAGACTTCTCCT | 57626 |
rs373579668 | snp | C/T | 1.73291e-05 | 0.00294351 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839170 | GCCAATATCTGTGAA[C/T]AATACACAATAGCTG | 57626 |
rs373593125 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039573 | TGCCATTTTATTTAG[C/T]TTTTTTTTCTCTGAT | 57626 |
rs373596895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964232 | AATTTTTTGTAGACA[A/G]CATCTTGCTATATTG | 57626 |
rs373606739 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69948098 | AGAGATTGTTTTCAA[A/G]AAAAAATGAAATGTT | 57626 |
rs373609195 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69896767 | TCTGCTTCCTGGGTT[A/C]AAGCAATTCTCCTGC | 57626 |
rs373620246 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69937645 | ATTAATTTTACACTT[A/C]TACCTGATGCTGAGC | 57626 |
rs373622839 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69801462 | TCTTAAACTCAAGAC[A/T]GCTGCCATTACAAAC | 57626 |
rs373651375 | in-del | -/GTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70041968 | CTTATTTCTTTGTTT[-/GTTT]CCTGTTGTGTTTGGT | 57626 |
rs373654967 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068234 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 57626 |
rs373668322 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69729162 | AGCACCACACATCGA[C/T]GTTTATTCACTTTTT | 57626 |
rs373672412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931954 | TAATAAAATTAGGCA[C/T]AAAAATATTTTAAAT | 57626 |
rs373678031 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69791454 | TAAAAAAATATGGAA[A/T]TACAAGGGACCCAGA | 57626 |
rs373682323 | snp | C/G | 1.81737e-05 | 0.00301439 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701664 | ATAAAAATAACCACT[C/G]CAGCAAGTAAAATCT | 57626 |
rs373684184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959217 | TCCAACTTTGTACAG[A/C]AGGATGCTGAGTATC | 57626 |
rs373697059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092616 | GAATGTAAAGCATTC[A/G]ATGGATTATATATAC | 57626 |
rs373703527 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061530 | CCTTTATCCAAGGAC[C/T]TGGATCCTCAAGCTG | 57626 |
rs373704179 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789384 | TTACTTTTTTTTTGG[A/C]AACAGCATATATGTT | 57626 |
rs373714745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735904 | ATTATAAGAAATATG[C/T]CTTACCTTTGCATTA | 57626 |
rs373720081 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70041835 | CACACTGGGATAGAA[G/T]ACCATGCTTGCTACT | 57626 |
rs373722851 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721354 | TCCCTAAAATGTATA[A/C]AATCAAGCTGTGCCC | 57626 |
rs373730947 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70081451 | TAACTTATTCCAGTG[A/C]ATCACAAAATTCATT | 57626 |
rs373736159 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70047279 | AAGCTTTTGGTTAAC[C/T]GAAAAAAAAAAAACC | 57626 |
rs373749342 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69803166 | TAAAGGTGTTTTGTG[C/T]AGGGAGTTTTAAATA | 57626 |
rs373750595 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721080 | ATATATATATATATA[A/T]AGCTATGTACCTCCC | 57626 |
rs373759595 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69738404 | GAGGCTGAAATGGAC[A/G]AATTGAGAGAAGCAG | 57626 |
rs373760715 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041078 | TAATTGTATATTGTA[C/T]AATTTCTCTTTGGTT | 57626 |
rs373761531 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69998006 | CATGATAGTTCTACT[G/T]TAATGTTGTGAAGAA | 57626 |
rs373787673 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69770362 | CATGCAGAAGCTTTG[C/T]TGGCCACGGAGGTTT | 57626 |
rs373803302 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69836330 | CTTCTCTGGGCGTTT[A/G]CTGATTTCGAAGATG | 57626 |
rs373816302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852553 | CACACTAATTAGAAG[A/G]TATCAGTCAGCATTT | 57626 |
rs373829176 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884426 | TGCCATCAGATTTTT[-/C]AAAAAAAAAAAAAAA | 57626 |
rs373853309 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69921007 | GTTGTTTTAGCACCA[A/T]CTTGGCAGATAAAAT | 57626 |
rs373869209 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69908646 | TTTTCAAATGTTATA[C/T]CTTGTACAATTATTG | 57626 |
rs373890580 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068312 | CGCCACTGCACTCCA[A/G]CCTGGGCGACAGAGC | 57626 |
rs373906799 | in-del | -/CAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69991388 | CTTTGAAAACAACAA[-/CAA]TGACAACAACAACAA | 57626 |
rs373913682 | in-del | -/TATAGA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69946238 | AAAACATTTGACGAT[-/TATAGA]TATATTCATTACTTT | 57626 |
rs373921718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824291 | AAAAAGCAAATAGAT[C/T]TATTAATAAATAGCC | 57626 |
rs373938155 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69879130 | TGATGGGTGCAGCAC[A/G]CCAACATGGCACATG | 57626 |
rs373948954 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70099047 | TTCAGTGTAACATGT[C/T]AAGAACACAGAAAAC | 57626 |
rs373950156 | in-del | -/A | 0.0298908 | 0.118541 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052337 | AAACTGATGAGAAAG[-/A]AAAAAAAAATATTTA | 57626 |
rs373957018 | snp | A/C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70032714 | TAAGTATTATTCTAT[A/C/G]CATTTAGAAACACAT | 57626 |
rs373961087 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69702427 | TTCTTTGGAGACAAG[C/T]CAACATTTTGATAAT | 57626 |
rs373964431 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70008993 | TTAATGTTCATGCTT[A/T]TATGATGCTTCAATA | 57626 |
rs373970390 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70012215 | AGCATTCTTCAACTT[A/T]CTGAAAACAAAAGTT | 57626 |
rs373976390 | in-del | -/CT | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046028 | TAATTTATTTATCTA[-/CT]CTCTTTCTCTAAAAT | 57626 |
rs373983483 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69727736 | TGGCATATATCTTAG[C/T]CAGTCAACTATTGTG | 57626 |
rs373985895 | snp | A/C | 1.65302e-05 | 0.00287486 | missense | KLHL1 | GRCh38.p7 | 13:69707729 | CACCAAGGAGACAGA[A/C]CCCAACAGCATCTCT | 57626 |
rs373986676 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950087 | CACAAGAAAGACATG[G/T]TTATGTTTTTTGAGT | 57626 |
rs373999211 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69739318 | TAACTATACAGACCA[G/T]TGACACTATGAAGCT | 57626 |
rs374003986 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70054765 | TCTGGAGCTGAAAAA[-/A]TTCAAAAGAAAAACT | 57626 |
rs374005286 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69907156 | TAACATAGGTTCATT[G/T]GTGGCTTATGTTTGT | 57626 |
rs374009118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814200 | TTACCATACGCAGAA[A/G]AATGAAACTGCACTC | 57626 |
rs374011034 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016444 | CGTAGGCTCGTAAGT[A/G]CCTGCTCTAGCTCCC | 57626 |
rs374023325 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804350 | GTACACTCTAGTTTG[A/G]CAATACAGACAGCAG | 57626 |
rs374024182 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69842788 | ATGGAATCAACCTAC[A/G]TGCCCATCAATGGGT | 57626 |
rs374026353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778100 | CTAAAGAAGATAGTA[A/G]AACAGTTAATTAAAG | 57626 |
rs374033723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908178 | ATGGGCTATGGGTAT[A/G]CCAGCAGAGTATAGA | 57626 |
rs374039295 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901167 | CTGGTTAAATGCAAA[G/T]ACTTATTTGGTTAAT | 57626 |
rs374039853 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014980 | TTAAGCAAAACAAAA[C/T]ATTAAGCAAACATGC | 57626 |
rs374051751 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69937992 | TCCCACGTGTAGTAG[-/A]AAAAAATGGAATGAT | 57626 |
rs374054884 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69865469 | TTACATGTAAATGAT[A/G]TGCGCATTTCAAAGT | 57626 |
rs374063364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835579 | AGGCCTTTGGTTCTG[C/G]GTTGAAGCAGATTCA | 57626 |
rs374082128 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897496 | GATCTTTCCAGTAGC[C/G]CAAAGATATCCTTGA | 57626 |
rs374093787 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69924739 | GGAGAGAAGAGCAGC[C/T]GCCCTTTAGGGAGCC | 57626 |
rs374122127 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70077722 | CTGTAGTTTCTTCTT[A/T]AATTTTCTGTAAAAA | 57626 |
rs374150187 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70036065 | CTTACATTTGAGGAA[A/G]TAATAATCATACTTC | 57626 |
rs374153656 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017728 | ACAAAATCCTAATGT[G/T]AAAAAGCAAAGAAAG | 57626 |
rs374171514 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69988446 | ACATGTGTCTTTATG[A/G]TAGAATAATTCATAT | 57626 |
rs374173536 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022194 | CTTTTCTTTAGATGC[A/G]GCTATCCAGTTGTTC | 57626 |
rs374178655 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69746695 | TCCCCGTGTGTCACC[C/T]TATTGTTGAGAGAAC | 57626 |
rs374186311 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996819 | AAATCTTACAAACTT[A/C/T]AAGTGGCCTATGACA | 57626 |
rs374196785 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69974298 | TGTTCAGAATAATAC[A/G]TATAAAGGTAATACA | 57626 |
rs374218110 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69785992 | TAGACCAATAACAGG[A/C]TCTGAAATTGTGGCA | 57626 |
rs374221124 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69767808 | TCTTCAATGATTCTT[G/T]ATGTGTCTATCAGAT | 57626 |
rs374222755 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837784 | ACCCCAGATGGAAGA[C/T]ATTTTATTGTGTTTT | 57626 |
rs374230222 | snp | A/G | 6.11191e-05 | 0.00552773 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940246 | AGCAGCCTAAACATA[A/G]GCAAAGATAATTATG | 57626 |
rs374231957 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773301 | TGACATTTACTATTG[G/T]CTCTTATTTGCATAT | 57626 |
rs374252425 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69816007 | TCAAGAGGAAAAATA[A/G]AAACCTCAAAATAAA | 57626 |
rs374256392 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901926 | CCTCAGCCTTCCGAG[A/C]AGCTGGGGTTACAAG | 57626 |
rs374257538 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69844658 | CTAGGTACAATTTGA[C/T]CATAATTTTATTATG | 57626 |
rs374261115 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980166 | ATTCTCAGGTGAAAC[C/G]TGTTTCCCTATTTCT | 57626 |
rs374268988 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69869099 | TCAACAAATATAAAA[A/G]TGTTGTATAAATTAT | 57626 |
rs374269390 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69944260 | TAAAACTCCAGGCAC[C/T]GAATCTCTAGTGAGC | 57626 |
rs374270422 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996536 | GTGTGAAGCTGTCAA[C/T]TTCCCATAACACTTT | 57626 |
rs374277719 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004536 | CCCTGACTAGTCCAC[A/C/G]TTTCCTTTTTTTGTA | 57626 |
rs374278446 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970634 | CACCACCTCTCCTGA[C/T]TCTCAACCTGTGGGT | 57626 |
rs374290162 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69970965 | ACCAAAACAGCTTCT[C/T]AGATCATTAGTTTCT | 57626 |
rs374334352 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70063055 | GGACGGTTAAATTTG[A/G]CCACAGATTCTGACT | 57626 |
rs374335314 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69819769 | TAGGCTCTGCTTTTT[A/G]TTCACAGCTATCATG | 57626 |
rs374351954 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | KLHL1 | GRCh38.p7 | 13:69796900 | GCAGCCTTCTGCCAT[C/T]CATCATCCCTGCCTG | 57626 |
rs374352042 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69860384 | TCAGAAAAAAGAGAA[A/T]GTTAGTGGCATTGTA | 57626 |
rs374352791 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70029631 | AAAGGAACAACTGGT[A/C]CCAGCCACTGCAAAA | 57626 |
rs374363622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009368 | ACACTAGGTGTTGCA[C/T]AGGTAAAGGGCAGGG | 57626 |
rs374371117 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70000486 | AGTAAGCCTGATTTA[C/T]TAAATATATAGAGAA | 57626 |
rs374371163 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69799002 | GCTAAGGCAAGAGAA[A/T]CCCTTGAACGTGGGA | 57626 |
rs374390867 | snp | C/G/T | 4.94697e-05 | 0.00497321 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107398 | CCTTGCTGCAGCCTC[C/G/T]TGGCAACTGGAAGCA | 57626 |
rs374409468 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786880 | AGACAAACAGAGCCG[A/G]ATCATGAGGGAACTC | 57626 |
rs374412887 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70032133 | TTGTAAACATTTAAA[A/G]GTATATCATCTGTGT | 57626 |
rs374445869 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69926676 | ATTCAGGCCGGGCGC[A/G]GTAGCTCAAGCCTGT | 57626 |
rs374466774 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69971665 | ATACTACTCATTTCC[C/T]TATTTGACTATGTCT | 57626 |
rs374484175 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69969575 | ATGCATAAAACGTAT[A/G]TAGTTGCAGCAAGGC | 57626 |
rs374496696 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69703952 | TTCATTTTTAAGGAA[C/T]GCATGACTGTATATG | 57626 |
rs374515986 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855337 | AGATAGATAGATAGA[C/G/T]AGATAGATAGACAGA | 57626 |
rs374518545 | in-del | -/AACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789532 | AAAATGACATAAACA[-/AACA]GTATAAATGACATAA | 57626 |
rs374518952 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69894573 | GCATATTTTCAGCAA[C/T]TTGAAACAATTCCCA | 57626 |
rs374535455 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69957251 | AATGCCAACAAGTAG[A/T]TAGTGATACATAGAT | 57626 |
rs374549745 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69859889 | TATCACATTGTAAGC[A/G]TACAAAAGCAAGGAC | 57626 |
rs374549805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967320 | ATAACAACTAGTTTG[A/G]AAAAAGAGAAGATTC | 57626 |
rs374554720 | in-del | -/TAATT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70008791 | ACAAAGATAGCAATT[-/TAATT]ATTCACCAGTATGAA | 57626 |
rs374560329 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69900878 | GCTGAGAAATACATC[A/G]CCTTGCATTTGGTTT | 57626 |
rs374560699 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69895850 | TAGGTGAGACTACAT[G/T]TGTGCACCACCATGC | 57626 |
rs374566903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846361 | CAGAATCAAACATGA[C/G]CAGGAAATATATAGG | 57626 |
rs374576634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008492 | CATGTGCGTCATTGG[C/T]TATGCACCCAAATAT | 57626 |
rs374584217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870682 | TGGTTATGCAAGCAT[C/T]GGGTAAACATTCCCA | 57626 |
rs374592194 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69757900 | AGGCAGAGGTTGCAG[C/T]CAGCCAAGATTGTGC | 57626 |
rs374592962 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69941220 | AACAAGTCTCAATCA[A/G]TTTAAGAAAATCAAA | 57626 |
rs374597477 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69980666 | CCTTATTTTTTTCAG[C/T]GAATTGTTTTTTATT | 57626 |
rs374624795 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839255 | TAATGTCTGTGATAT[G/T]ATCCTTATATTGAGC | 57626 |
rs374649221 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70074953 | AATACTTAGAAAATG[A/G]AAATTTAAAATACCA | 57626 |
rs374650034 | in-del | -/ACAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70059089 | ATACTAAAACCTCAA[-/ACAA]TGAAACTACTACAAG | 57626 |
rs374650351 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69987445 | ATTTTCAGCTATTCA[A/G]TAAAAATCAGCTTTT | 57626 |
rs374656175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978160 | CAGAATTCTTCCACC[C/T]GTTAACGCATTGAAT | 57626 |
rs374664847 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69972397 | ATTTTTAAATGCCAA[-/G]TGTTTTAGTCTGTAG | 57626 |
rs374680431 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69946225 | AAAAGGACATGAGAA[A/G]ACATTTGACGATTAT | 57626 |
rs374717086 | in-del | -/AAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69940793 | TTTTATCTTAAAGGC[-/AAA]AAAAAAAAAAAAAAA | 57626 |
rs374725160 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976956 | GAGTGAGAGTCCAAG[G/T]AGCTCAACATAATAT | 57626 |
rs374725892 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70036835 | TTTTAATGCCATGGT[-/C]TTTTTTTTTTTTTTT | 57626 |
rs374739657 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70081862 | GTGGTAATTTGTTAA[G/T]CAGGAATGGAAAACT | 57626 |
rs374740009 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69711031 | ACGATAGTCACAGAA[C/T]AAAAGTTAATTTCTC | 57626 |
rs374742057 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70025168 | ATTATAGTTAAGGTC[G/T]TTGGACTAATTTTCC | 57626 |
rs374744411 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69951410 | ACTGGCCAGATTTTC[A/G]CAAGTTAGTAGGAAC | 57626 |
rs374747920 | in-del | -/AATAAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69982438 | AAGACTCCATCTCCA[-/AATAAT]AATAATAATAATAAT | 57626 |
rs374750237 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086614 | AAAGAAAGAAAGAAA[A/G]AAAGAAAGAAAGAAA | 57626 |
rs374753705 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974738 | CGCTGAAGAATATAA[C/T]TGAATTATTAACTAG | 57626 |
rs374766226 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69909719 | AGATATGGCTGTGTG[A/G]AGATAATACACAAAA | 57626 |
rs374778836 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70018416 | AGAGTTAATTCAGCA[A/G]CTGTTCTAGCAGTAC | 57626 |
rs374791266 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70024351 | TGAATTGTAAGACCT[A/G]GATAGAAAGATAGAG | 57626 |
rs374808176 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69778464 | TTTCTATTCAGTCCA[C/G]AAATTCTTAACATCA | 57626 |
rs374809595 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69740892 | TATAAAATAATACTA[A/C]TTCCCATATTTATGA | 57626 |
rs374814606 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107199 | CCGTGGGGACTTACT[A/G]TACCTGTGTCCACAT | 57626 |
rs374819215 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884973 | GAGTCTCGCTCTGTC[A/G]CCCAGGCCGGACTGC | 57626 |
rs374821680 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69858317 | AGGAGAGATAGACCT[A/C]ATAAGGACTTTGAAC | 57626 |
rs374826189 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69912546 | ATTCTACTTTTTCAG[G/T]TTCTTTTTAAATTTT | 57626 |
rs374827295 | snp | A/C | 0.000709109 | 0.0188163 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975581 | CTGGCACTTTTAAAC[A/C]TGTGAATGCATGTTT | 57626 |
rs374860601 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69978167 | CTTCCACCTGTTAAC[G/T]CATTGAATAGAAAAG | 57626 |
rs374877437 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022905 | TTCAAGAAAGATAAA[A/G]TTTACACTGAGTAAA | 57626 |
rs374913724 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69960299 | GAAATGCTGTAAAAA[A/T]TAAAACTCCTTAAAC | 57626 |
rs374914247 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69755059 | GTCCTCCAAATCTTA[A/T]GTTGAAATGTGATTC | 57626 |
rs374920177 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996901 | AAAAGTTCTTATTTT[A/T]TTCATTAAATTTTTT | 57626 |
rs374923948 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69904171 | AATAATAGAAAAATA[A/C]AATGCATTAAGTTTG | 57626 |
rs374926138 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961607 | AAACTGATTCAAAAA[C/T]TCTTCCCCTAACTTT | 57626 |
rs374927704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082172 | GCCATGGCTCCTGTA[C/T]AGCCTGCAGAAATGT | 57626 |
rs374949036 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703772 | GCAATTACCTAGAAT[A/T]CTCATTACGGTAACA | 57626 |
rs374958269 | snp | A/G | 3.34253e-05 | 0.00408797 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961456 | AAGCCTGAAAGAGTC[A/G]CAGGTTCTAATTTAG | 57626 |
rs374960721 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69975083 | ATCATTTTAATGAAT[A/G]AAACTATTAGCTTTC | 57626 |
rs374960770 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70005819 | CATTAAATCAATAAA[A/G]TATTGTCATATATTA | 57626 |
rs374969062 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69988181 | TGTTCTCGCATTACT[C/T]AGCTGCTACTTATAA | 57626 |
rs374969236 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050718 | AATCATGATCAAAAT[A/G]TAAGTGTTAACCTGG | 57626 |
rs374977872 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084832 | AATTCTAAAGAATAT[A/C]AAAAATATTTTTGTT | 57626 |
rs374986943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813452 | ATGTTGTGCACATAT[A/G]AAAAAATACACACAT | 57626 |
rs374992946 | in-del | -/TGTGTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730268 | GTACTAACACTTTAA[-/TGTGTG]TGTGTGTGTGTGTGT | 57626 |
rs374995735 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69711181 | AAAAACATTACTTTC[C/T]TAACAAATAGAATTG | 57626 |
rs375000093 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69830751 | TATATCAAGTACTCT[C/T]TCAGACCACAGTGGA | 57626 |
rs375009287 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69940406 | TTTTAAGAATTTTGC[A/T]TTTCGTATTTCATGT | 57626 |
rs375013579 | in-del | -/TGGA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69755091 | AATGTTGGAGGTGGA[-/TGGA]GCCTGGTGGGAAGTG | 57626 |
rs375014526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910667 | TCAGACAAAAAATTC[A/G]TATAAAACACTCAAA | 57626 |
rs375021933 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69979654 | AGTTTCTTTCCAATC[G/T]AAGAGTCCCTTATAC | 57626 |
rs375025376 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70024661 | CTCTCTCTCTCTCTC[G/T]CTCTGGCTCTGTCTC | 57626 |
rs375027029 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69938105 | AACATATGCCTGATT[G/T]GACAAGGATCAGAGG | 57626 |
rs375027713 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69865112 | TGTATATTGTTTAAT[A/G]TTTTTGTAGAGATGG | 57626 |
rs375035282 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70006325 | TAAACCCCACTTGAT[C/G]AAGGTGAATGATCCT | 57626 |
rs375043213 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769672 | CAAACATATAAAAGC[A/C/T]CAGGACTCAGCCACA | 57626 |
rs375048077 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69761917 | CTAAATTGCTAAGAT[A/G]GTTTATGATCAATCT | 57626 |
rs375095324 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69713997 | GGCTCTTATGCTGAT[A/G]ATGTGCTTAATGTCT | 57626 |
rs375099707 | in-del | -/CCA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69757793 | AATCTCGTCCCTACT[-/CCA]AAAAATGCAAAAAAT | 57626 |
rs375102616 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69877709 | TAACTGAATTTGTTT[C/G]TGGATTAGTTATTAT | 57626 |
rs375102814 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69755177 | GTGAGTTCTAGCTCC[C/T]TGAGTTCACAAGAGA | 57626 |
rs375105269 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69771844 | AATTAGGAAGACATG[C/T]GAATCAAAATGTGGA | 57626 |
rs375106649 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69900094 | CCTTCAACCTTGGAG[C/T]GGGGCAGACATTTAT | 57626 |
rs375118065 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960361 | AACCTGCCTTTCTTC[A/G]TCTCACACCAGTATG | 57626 |
rs375125641 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70034451 | GCTATTCATTGACCA[A/G]TGGGACTCAGCAGTT | 57626 |
rs375152771 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917521 | ACTCAGTAACAGGAA[C/G]AAGAAACCCTTGGAG | 57626 |
rs375165596 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69924389 | CCCCTCTGAAGCCCA[C/T]AAAACCCCCCAGACT | 57626 |
rs375173168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881403 | AAAAATGTTGATTGT[G/T]ATTTGGATTCAAATG | 57626 |
rs375183558 | in-del | -/GTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70081899 | TTGGTCACTGATATT[-/GTT]TGGATTTATGTCCTC | 57626 |
rs375188365 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69921658 | TGTTTCCCTTTTACA[A/T]GCCCTCACTCCAATA | 57626 |
rs375199118 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69924292 | AGCCTGAGGGCTGTG[A/C]TGATGGAACAGAATG | 57626 |
rs375203137 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69880357 | AACAGAAAATATTTC[C/T]GTTCATTCCTCCTGC | 57626 |
rs375205136 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69941372 | CAACAATGAAATCAA[A/G]GTGGAAATTAAAAAT | 57626 |
rs375238256 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69844758 | ATAAGGTTTTTCTTC[G/T]GGGTTTTTTATTTAT | 57626 |
rs375239319 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69720163 | ACAATGTTAGTATGA[C/T]TGAAAATTGCTGAAG | 57626 |
rs375256750 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70019772 | ACTAAAAATCTTTAA[-/C]GATTTAAATGGTGTT | 57626 |
rs375257585 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69904531 | ATCTTATTCCCATTA[G/T]CCCTGGTACTATATA | 57626 |
rs375273515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831716 | AAAATACTAGCTAAA[A/T]AAATCCAACACCATA | 57626 |
rs375300999 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69893221 | TTCTCTTGGTAGCTA[A/C]ATAAATTTTTTTTTT | 57626 |
rs375308184 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918299 | TTTTATGTATTGCCA[G/T]ATTTTAATTAGTTGA | 57626 |
rs375311225 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110412 | ATTACGCATGAAGTT[A/C]TGTTAAACTGAAATG | 57626 |
rs375316223 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69725965 | GCAGGGTTATGTCTA[C/T]TCATCTCTCAGTCAG | 57626 |
rs375321270 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936798 | ACCTTCATTTCAACA[A/T]GAATTTTCTCAAAAG | 57626 |
rs375324723 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69891124 | AAAAGTTACTAAATG[C/T]CATACATGTTTTGTT | 57626 |
rs375332427 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70095158 | ACCCAGCATAATGAA[C/T]GGTATCGGTTATAGA | 57626 |
rs375337735 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773882 | ATATATATATATATA[C/T]ACATAGAATAAAACG | 57626 |
rs375340598 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69903605 | TTTTTTGCAGATTCC[G/T]TTGCAGAAAACCCTT | 57626 |
rs375352920 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69808425 | CTTAGAAAGCCACTA[C/T]ACAAACCTTTCTGCA | 57626 |
rs375360552 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016597 | TTCTGTTTCAGCCCC[C/G]TCTGAATTTTGGGCA | 57626 |
rs375360679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963592 | CACAAAAACAAGCTG[C/T]ACAGCAGATGTGGCC | 57626 |
rs375368796 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69972153 | ACATAGAGAAGCAGT[A/G]CTATCTGCCTACTCT | 57626 |
rs375373479 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70048717 | GATCTGACAGGAGGA[A/G]GAGTTCAGGCAGTGA | 57626 |
rs375376132 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70004535 | CCCCTGACTAGTCCA[C/T]GTTTCCTTTTTTTGT | 57626 |
rs375379857 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103469 | TGGAAAAATATTTCA[C/T]CATTCTTAATTTTTA | 57626 |
rs375385988 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70071260 | GACTTAAAAATTAGA[A/C]GATATAAAGAGCAGC | 57626 |
rs375406570 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69922139 | TTTAATATAAAGAAT[-/AT]CTCACCTTGTTACCC | 57626 |
rs375418523 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69707900 | AAAAAGGAAACTACC[-/T]TTTTTTTTCTCTAAA | 57626 |
rs375420633 | in-del | -/CTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69895095 | TCTTGCTTTCTTCTT[-/CTT]GCTTTTCTTCTAATG | 57626 |
rs375453581 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69752370 | ATATTGTTCCAGAAT[A/C]TTCCACAAATATTGT | 57626 |
rs375454065 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69734821 | ACTATATATAATAGT[G/T]TCCATAAAACTTCTA | 57626 |
rs375456221 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69736824 | ATGGAAAACCAAACA[-/TA]GTATATTCTCTCGTA | 57626 |
rs375462946 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70102195 | CCACTAATCTCCATG[A/G]GATTTTTAATGGTGT | 57626 |
rs375473154 | snp | G/T | 0.0543475 | 0.155628 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935197 | CCAGTACCAACTATG[G/T]ACCACGTTCACCAGT | 57626 |
rs375475608 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69796591 | AATAGTGAGCCAAGA[A/C]ATTTTTCTATGTTAA | 57626 |
rs375479750 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703410 | AACTATTACTATAAA[-/AG]AGTCAAAAAGTTTTT | 57626 |
rs375482776 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69982965 | ATGTAGAAAACCTTA[-/AA]GAGTCCACCTAAAAT | 57626 |
rs375483923 | snp | A/C | 0.194036 | 0.243656 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774672 | ACTTAATAAAAAAAA[A/C]CACACACACACAAGC | 57626 |
rs375491092 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69736996 | TGAGGTACCAATTTT[C/G]TCTTATTAGGACTGA | 57626 |
rs375492945 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69736757 | AAATAATGGCATTTG[C/T]AGCAACCTGGTTGGA | 57626 |
rs375497641 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806107 | TAAGAGTGGTTATAC[A/G]CATCAATGGAAAACA | 57626 |
rs375499431 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876322 | GGTCATGAAGAGTCC[A/G/T]TATGTCACTGGTATC | 57626 |
rs375499595 | in-del | -/TAGA | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946411 | ATTTGAGTTGACAAG[-/TAGA]TAGAAACATTTTCTG | 57626 |
rs375505163 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70020054 | TCACCTAATGCCATA[C/T]GCCATCACCTTGATC | 57626 |
rs375508018 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69854049 | CATCCTGATCCTAGA[A/G]GCAAAATTTAACTTT | 57626 |
rs375514179 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705690 | AAGTAACTTAACAGT[C/T]TTAAATTTAATGTTT | 57626 |
rs375520965 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69990845 | CCACTCAGAGATGAC[A/G]GAATATATACTTTTT | 57626 |
rs375527681 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69891885 | AAGGAGCCTATAGAA[A/G]TAATTTATAAATTTT | 57626 |
rs375533193 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69728510 | GCCTCCGCTTCCCAG[C/G]TTCCAGAATTATTAG | 57626 |
rs375538331 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69940761 | TTTTTCTTTGTTTTT[G/T]TTTCCCTGTTTGGTC | 57626 |
rs375555693 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078966 | TTAGCATCAAACTCT[C/T]ACCTCTTCCATTTGA | 57626 |
rs375569092 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69849604 | TTTCATGAAGATTTA[C/T]TTCATCACTCAGGTC | 57626 |
rs375572650 | snp | C/G | 3.29902e-05 | 0.00406128 | missense | KLHL1 | GRCh38.p7 | 13:69719444 | ACTGCATAAAGAAAA[C/G]CGTCACATGTGGCCA | 57626 |
rs375587372 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884344 | TGTGTTTCCTTTGGG[C/T]ACCATGTAAATTATA | 57626 |
rs375592542 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69931519 | TTTTGTCCTTTTCTA[C/G/T]TTACTATTATCCAGC | 57626 |
rs375594798 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70006775 | CTAGATTACTATTGA[C/T]ATATATATGCTAGAA | 57626 |
rs375600830 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69939380 | ATATATATATATATA[C/T]ACACACACACGCACA | 57626 |
rs375642620 | snp | C/T | 1.65384e-05 | 0.00287557 | missense | KLHL1 | GRCh38.p7 | 13:69707668 | TAGGATTCCATAGTG[C/T]TGAGGTATGTCTGTC | 57626 |
rs375668308 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69768600 | AGAAAATTTTCTCTA[A/T]GAAAAAATTATACTG | 57626 |
rs375670370 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69822067 | AGCTGGGTGTAGTGG[C/T]GGGTGCTTGTAATCC | 57626 |
rs375671069 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097839 | TAAAAATTCAAAAAA[-/C]ATTCAGAGAATTAGT | 57626 |
rs375688962 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69776340 | AAAAAGCAAAGCAAA[A/G]TGAAGCAAAGCAAAA | 57626 |
rs375695692 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102962 | CTCCACTTGGAAATT[A/C]ACTTACAGACAAACA | 57626 |
rs375698969 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780731 | GTATATATATATATA[C/T]ACATATATATATACA | 57626 |
rs375712889 | in-del | -/TGGTGC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69783700 | AAATCTACGTCTGAT[-/TGGTGC]TGATTGGTGTACCTG | 57626 |
rs375724042 | snp | C/T | 1.69266e-05 | 0.00290913 | missense, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107521 | ACACCGCTTCTCTCT[C/T]GGCTTTTGAGCAGGC | 57626 |
rs375739847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708580 | TAATTCAAGAGATCA[A/G]AGTCAGAAGACTGAA | 57626 |
rs375754687 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69879550 | AAAAGCATGGACAAA[C/T]CTTACGTTAATGAAT | 57626 |
rs375756052 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69811407 | TAGATAAAAAAAAAA[-/A]GCATTAGATAAAATT | 57626 |
rs375783377 | in-del | -/GGC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69940790 | TCATTTTATCTTAAA[-/GGC]AAAAAAAAAAAAAAA | 57626 |
rs375817678 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714469 | TTTAAAAATTGGATA[C/T]GCTTAACAGTTCAAA | 57626 |
rs375826936 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69871071 | GACTCCCAGGCTTTC[G/T]GATACATCCTCTGAA | 57626 |
rs375834887 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69953441 | TGTTGAATAACTCTA[G/T]ATCTAGTAGAAAAGA | 57626 |
rs375844545 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69736096 | ATCAGCAGAATAAAC[A/G]GACAACGCACAGAGC | 57626 |
rs375848712 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70101454 | TTTTTTTAAGACGAA[A/G]TCTCGCTCTTGTCCC | 57626 |
rs375850580 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69729172 | TCGACGTTTATTCAC[-/T]TTTTTTTGTGTGTGT | 57626 |
rs375860665 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69979290 | AGGTCATTAATCTTT[C/T]AGATAAATGGTTATG | 57626 |
rs375865357 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068285 | GGCGGAGCTTGCAGT[C/G]AGCCGAGATCGCGCC | 57626 |
rs375869545 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084328 | AACAGATCATTAAAC[C/T]TTTCCATCTTAATCT | 57626 |
rs375869705 | snp | A/G/T | 3.29523e-05 | 0.00405898 | missense | KLHL1 | GRCh38.p7 | 13:69796821 | TCAACAGTGTTCAAT[A/G/T]TCTTTAAGCCATCTC | 57626 |
rs375869784 | snp | C/T | 7.32681e-05 | 0.00605216 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707839 | CATATTCTAATCACA[C/T]TCAACTTTTACTATA | 57626 |
rs375871730 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69724886 | AACCAAATTTGCCCA[A/G]TAAAAAATCTATTAT | 57626 |
rs375876201 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69987905 | ATGTAGAATAAACTG[C/T]TACTTACAAACAAGT | 57626 |
rs375881243 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70032599 | GTTAAAAATGAATCC[A/T]ATACCTCCACAACCA | 57626 |
rs375888628 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69890080 | AGGCTCTGGCCTTAA[G/T]AATTTTACTTTCTAG | 57626 |
rs375892648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901828 | CTGAGACGGAGTCTC[A/G]CTCTTGTTGCCCAGG | 57626 |
rs375897689 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947869 | AAAAGTTAACTTTTA[A/G]AAAAGCATGAAAACT | 57626 |
rs375901774 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69713934 | AGAGGAGAAAGCAGT[C/T]AGCACAATGTTAGAA | 57626 |
rs375903420 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962580 | GAATATACTTGGAAT[A/G]TAAGCTTTACTAAGT | 57626 |
rs375906017 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69818824 | GAACCAAAGTGACTG[A/C]ATGTAGTCACTGAGG | 57626 |
rs375906935 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068827 | ACTTAGCTTATGGGT[A/G]AAAAATGTCTTAGGG | 57626 |
rs375922691 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69791277 | TTAGCAAAATAGGTA[C/G]AAGACTAGGGACCTA | 57626 |
rs375941697 | in-del | -/ATT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70013627 | TGGTGAACAAAATGA[-/ATT]ATGTTTCCTTAGAAT | 57626 |
rs375944876 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69914095 | GCACTCCAACTTCTT[C/T]AGCTTTGGGACTCGG | 57626 |
rs375945399 | in-del | -/TTAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855208 | CAGACTGTCTACTAG[-/TTAG]AGTGTAGAAAGACTT | 57626 |
rs375946197 | in-del | -/CT | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020812 | TATATGCATACATAC[-/CT]ACATACACATATATA | 57626 |
rs375949010 | in-del | -/TAGA | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074861 | CACAGCATGATTGTG[-/TAGA]TAAAAAATTTTAAAT | 57626 |
rs375958962 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69755885 | CTGGCTGTTTGCATT[C/G]AGCCTAATCACTTAT | 57626 |
rs375966863 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822193 | ACAGAGGGAGACTCC[A/G]TCTCAAAAAAAAAAA | 57626 |
rs375987447 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70076791 | CCAAAACACAACAAT[A/G]AGAAAAAGAAACAAC | 57626 |
rs375991720 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70037779 | AAATACACACATTAA[C/T]TGGGCTTTCTAACTT | 57626 |
rs376010040 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69724879 | TATATTAAACCAAAT[C/T]TGCCCAGTAAAAAAT | 57626 |
rs376021708 | snp | A/G | 3.3325e-05 | 0.00408184 | missense | KLHL1 | GRCh38.p7 | 13:69940096 | CTTGAGCATCTGCGA[A/G]GGCTCGAATTCCTAA | 57626 |
rs376025848 | in-del | -/AACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69808870 | TATTGGAAAGAACCA[-/AACA]GATTTTCTGCAATTA | 57626 |
rs376047957 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69933832 | AAAAAAAATCACAAA[G/T]TTCTTTGGTCTTATT | 57626 |
rs376063573 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69938077 | AAAGCACAGATTGGG[C/T]AGATTAGATGAGAAC | 57626 |
rs376064667 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70076270 | AGAGAGTGTAGTACT[A/G]GTGAAATAACAAACA | 57626 |
rs376072392 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69991015 | TTGCTCAAAACCATA[A/C]AATTACATGGGTATT | 57626 |
rs376082241 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907361 | CAAAATGGCAAATAT[A/C]TATTGTAATATTCTG | 57626 |
rs376082491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930644 | AATATGCCATTGTTG[C/T]TTATATATTATTTAC | 57626 |
rs376090861 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70002831 | AGTGGGAGAATGGGC[A/T]TACATTTACATGATC | 57626 |
rs376097027 | snp | C/T | 0.000102088 | 0.00714377 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838930 | ATAAAAGCTGCAACA[C/T]GGTATAACACAGGAT | 57626 |
rs376098520 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69986627 | GTGTTGCCAAAAAAA[A/G]TTCTATTATGAAAAT | 57626 |
rs376098942 | snp | A/G/T | 0.000305939 | 0.012365 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107170 | GAGTGGAAATTGAGA[A/G/T]ATGCTTGGAAGCCCC | 57626 |
rs376109579 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719205 | GTGTGTGTGTGTGTG[A/T]GTGTGAGAGAGAGAG | 57626 |
rs376116643 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69707033 | AACTTCCTGGACAAA[-/A]TGATTGACAAGGAGT | 57626 |
rs376142915 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810616 | CAACCTAACCGAACA[A/T]CCAAAGGAACTAGAA | 57626 |
rs376153514 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837276 | CTAATGGTGGCATTA[C/T]TTATAAAAAAATTAT | 57626 |
rs376168535 | snp | C/T | 9.9295e-05 | 0.0070454 | missense | KLHL1 | GRCh38.p7 | 13:69961343 | AGGTCCCAGAGAGCA[C/T]TGGGGTCTATGCCTT | 57626 |
rs376182795 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69899658 | AGTTAGGAACATACA[C/T]GGCTTTCTAGGCACT | 57626 |
rs376189037 | in-del | -/A | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755649 | CTCCAAAGTAATTTT[-/A]AAAAAAAAGCACTGC | 57626 |
rs376193296 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69796482 | TTGCTTCCTGTGTAA[A/C]CATGTGATCTCTGAA | 57626 |
rs376200715 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885436 | GTTATTTTTTTTTTT[C/T]CTTTACACTTCATTG | 57626 |
rs376210169 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70104486 | TCTAACCGGTTTACT[C/T]AACTGAGCTAGTCAT | 57626 |
rs376216084 | in-del | -/GATA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70077523 | GATCCTAAAATAATA[-/GATA]CATGAAATTATGCAT | 57626 |
rs376224508 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044209 | GTTTGTATTTTTAGA[A/G]CTCTACATTTGCTCC | 57626 |
rs376239310 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70004081 | ACTTTTATCTGAGGC[C/T]TACCTTTAAGGCCAA | 57626 |
rs376242769 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69893304 | CAGTGGCGCAATCTC[C/G]GCTCACTGCAAGCTC | 57626 |
rs376245447 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69956743 | AGAGGCTTTGAATAT[A/C]TAACTGTGTCCTCAT | 57626 |
rs376259621 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085599 | CTGGGCGCAGTGGCT[C/T]GTGCTTGTAATCTCA | 57626 |
rs376267562 | snp | A/G | 7.01484e-05 | 0.00592193 | synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107574 | CTCAAAGCTGCCACT[A/G]CCGTCCTGTTGCAGG | 57626 |
rs376283269 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057441 | TGAGGCCAGTATGCC[A/C]TGATATCATAAATAG | 57626 |
rs376292418 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70096646 | TTTATAAAGTTAGCT[G/T]TTTTTTTTTTAAAGA | 57626 |
rs376327865 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060850 | AAACTTCGTCTCAAA[A/G]GAAAAAAAAAATGTG | 57626 |
rs376330425 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69807514 | TAGACTGCTGTTGTT[A/G]GACTGAGACATGAGC | 57626 |
rs376344033 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69797592 | GAGGCCGAGACGGGC[A/G]GATCACAAGGTCAGG | 57626 |
rs376351139 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69712182 | CCTCTAAATGGTATC[C/T]TCTGAAGACATTTTA | 57626 |
rs376359971 | in-del | -/TTTTTTTTTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69996911 | ATTTTATTCATTAAA[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT | 57626 |
rs376372413 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855419 | AGATACAGATAGAGA[C/T]AGAGACAGAGATAGA | 57626 |
rs376375244 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975611 | TCCAGTAGAGGCAGA[C/T]TACTGTACCTATGTG | 57626 |
rs376376802 | in-del | -/AACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69790550 | CTTCCACAAAATACT[-/AACA]AACAAACAAATAAAG | 57626 |
rs376379939 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69829786 | CTAGAAACTATTGGG[A/G]TCTTATCTTTAGCCT | 57626 |
rs376385022 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852858 | TTTACTGAGAAAAAA[A/C]TTCAGGAATAAATGA | 57626 |
rs376386321 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068258 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 57626 |
rs376392758 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996396 | TTTGGAAGATAAAAA[A/T]GTCAGATGGATTTCA | 57626 |
rs376396046 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69886838 | TCAATTACAGTAAAC[C/T]CCTAGTCACGGTTCT | 57626 |
rs376400008 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69764983 | TTGAGACCAAGTCTC[A/G]CTTTGTCGCCCAGGC | 57626 |
rs376413496 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824168 | CCACATTAAATAAAA[A/C]TACATCCTATAATTC | 57626 |
rs376414250 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69800194 | GACATTGACCCTTGT[A/G]ATTACAATGGGCTCA | 57626 |
rs376420324 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69790565 | TAACAAACAAATAAA[-/G]AAATACAGCAAAATA | 57626 |
rs376420787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714993 | CATGCAGATAAATTA[C/T]CATGATGCCAGAAAA | 57626 |
rs376428396 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69925798 | TATATTACCATCATG[C/T]TGTTACTCTCATTCA | 57626 |
rs376433355 | in-del | -/ATCT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780029 | GGCTTGTCTCTATCT[-/ATCT]CCTGATCTCGGGTGA | 57626 |
rs376441155 | in-del | -/TCGAGGAAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69950543 | CATGTCATGCAACAC[-/TCGAGGAAA]TCGAGGAAATTTTGA | 57626 |
rs376441745 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955250 | TTTTTAATATTAAAG[C/T]AGGACATTAAACATC | 57626 |
rs376493587 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69844787 | ATTTATTTATTTATT[A/T]AGACAACAAACATCA | 57626 |
rs376508287 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70084005 | AAAGTCACTCAAAAC[A/G]CAAAAATGATAGAGG | 57626 |
rs376519002 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068319 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 57626 |
rs376533060 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69746711 | TATTGTTGAGAGAAC[A/G]CAAATGATTGAGTTT | 57626 |
rs376541987 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70033483 | ATTTTTATTTTTTGT[A/G]TTTTTAGTAGAGATG | 57626 |
rs376549782 | in-del | -/CAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69985144 | AAACAACAACAACAA[-/CAA]AAAACCTCTGTGCAA | 57626 |
rs376563134 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69793077 | AGCAGAAACAACCCC[G/T]ACCATATATTTAATA | 57626 |
rs376568793 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722085 | CAGGGACTTTACTTA[C/T]GGGCATCTTTCTGTG | 57626 |
rs376575059 | snp | A/C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69950112 | TTGAGTACTAATTAC[A/C/G]TCTCAGAGTTCAAGA | 57626 |
rs376589020 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782523 | GATTATATCCTGCAC[A/C]TGGCTTGGAGGGTCC | 57626 |
rs376606246 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69869187 | CCTGAGGAAGTTAAG[C/T]GACAGAAGCCTAAAA | 57626 |
rs376613869 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027084 | AAGATATATTCTTAA[A/G]TACAAAAACAAATAT | 57626 |
rs376620220 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70021829 | CATTTTTAAGAAATT[A/G]GTTTTTGTTTTGTTT | 57626 |
rs376629751 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995863 | TCAGAAACTGTCACA[A/G]TTCTCATATTGAGGT | 57626 |
rs376632517 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70079564 | CATCAGTTTACAGGA[A/G]CAGACTAATGTTTTT | 57626 |
rs376634403 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976154 | ATGAAATGTTAATTT[C/T]GTTCATTTGATATTG | 57626 |
rs376654295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906965 | AAAGAAAATGAGTTC[A/T]CACTTTTCTGATTAA | 57626 |
rs376662373 | snp | C/T | 1.6501e-05 | 0.00287232 | missense | KLHL1 | GRCh38.p7 | 13:69719463 | CACATGTGGCCACTC[C/T]GACACCCCCTCTCCT | 57626 |
rs376670996 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69729036 | AAAAGACATCTTAGC[C/T]AGAATGTAAAGTGCA | 57626 |
rs376673706 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70078654 | TTGCCTTCAAATCTA[C/T]AAAAGAAGAATGTAG | 57626 |
rs376675638 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039824 | TTTAAAATTTTTAGT[A/G]CAGATGGGTTTTCAC | 57626 |
rs376677651 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69853898 | TTTGCTTAGCGTAAG[G/T]CTTAATAATAATCAC | 57626 |
rs376680284 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936962 | CTTCCTGCAACTGCC[C/T]GTGGAGAATAATGGC | 57626 |
rs376682207 | in-del | -/ATC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69724602 | ATACATACAAAAATT[-/ATC]ATCATAATACCTGCA | 57626 |
rs376683526 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781285 | CTCCTTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 57626 |
rs376684907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853647 | GATAAGTGTTTAAAG[C/T]GGTATTCACCAGTGA | 57626 |
rs376695840 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780725 | ATATATGTATATATA[C/T]ATATATACATATATA | 57626 |
rs376701134 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992952 | GTACCTTTCTTACAG[C/T]GTCAGTAACTCAGCT | 57626 |
rs376712172 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69821227 | CTGCTTTTAAAATAT[C/G/T]CATAAATCATAAATT | 57626 |
rs376718836 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69836185 | AGACCTTGCAATGCA[C/T]GTGGGCTGAGGCCTC | 57626 |
rs376729624 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885141 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 57626 |
rs376731672 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70080843 | TGACCTCAAGCAATC[C/G]TCCTGCCTCAGCCTC | 57626 |
rs376738812 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69743409 | AGATAAAAGTGAAAA[C/T]ATTTGAAATATACTC | 57626 |
rs376748847 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69802885 | TGGCTTGTCCTGCTA[C/T]ATTTCTGGGTTCCTA | 57626 |
rs376754167 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938782 | ATTACAAATTGCATA[A/T]CTTCTTCCTTTTATT | 57626 |
rs376755591 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70058439 | TATGCCAAGAGTGAA[C/T]AATCTGAAAAAGAAA | 57626 |
rs376764722 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69963214 | ACAGCATGCACAACC[A/C]CCTCACCTAGCATGG | 57626 |
rs376773605 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70100007 | TTTTTCAAAAAATTA[C/T]TTTGTTTATTCTAGG | 57626 |
rs376782775 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068116 | GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG | 57626 |
rs376791925 | in-del | -/AG | 0.460813 | 0.134379 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785595 | AAGATCACAATTAAA[-/AG]AACTAGAAAAGCAAG | 57626 |
rs376818745 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034275 | TATTCACACAACTGA[C/T]GAATTTTGACTGTAG | 57626 |
rs376826644 | in-del | -/CAGGAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789045 | CTATCTATCTATCTA[-/CAGGAC]TCTATCTATCTATCT | 57626 |
rs376841004 | snp | C/T | 0.000307953 | 0.0124049 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940013 | CACAGAGTGTGTCTC[C/T]ATTATTAAAACATTA | 57626 |
rs376847916 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69751112 | TCATGTCATGTGTGT[A/G]TGTGTGTGTGTGTGT | 57626 |
rs376864097 | snp | C/T | 3.54868e-05 | 0.00421214 | intron-variant | KLHL1 | GRCh38.p7 | 13:69701787 | AGATGAAACACAACT[C/T]AAGACAAGTTTTCAT | 57626 |
rs376864873 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69776135 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 57626 |
rs376872090 | in-del | -/AT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70099139 | CTGATATAAACACAT[-/AT]GAGAAGTTTTTTAAG | 57626 |
rs376885508 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69805481 | TAATAACTAAAAATT[A/T]TTACCTTTAAAATCT | 57626 |
rs376887058 | snp | A/G | 0.000652539 | 0.0180511 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69839016 | AGCATACAAAGTTCC[A/G]ACTGTAGATTTTCTG | 57626 |
rs376900306 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69769107 | AACATACCCACTATG[C/T]ACCAGGAGTACAGAG | 57626 |
rs376902247 | in-del | -/AC/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69757791 | GAAATCTCGTCCCTA[-/AC/C]CTAAAAATGCAAAAA | 57626 |
rs376909230 | in-del | -/TTA | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052881 | TATCTTCTAAATAAT[-/TTA]TTATTTTATTCCTTA | 57626 |
rs376915441 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952688 | GTTTTCCTGGTTGGA[-/T]TGCACTTAGCATCCT | 57626 |
rs376916489 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69819984 | GTATGCAGGAAAGTT[C/T]ACTTGGCATTGTTTT | 57626 |
rs376931850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096860 | CTTCTCAGCAAAAGA[C/T]AGTAGCAAGAAAAAA | 57626 |
rs376946205 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721087 | TATATATAAAGCTAT[A/G]TACCTCCCTTACAAG | 57626 |
rs376949302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875999 | ATGATTGTTAATGGA[C/T]TGTGTTAGTGGGCTT | 57626 |
rs376949621 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70078120 | TGAGAAAGGAAGGAT[G/T]TACAGAGCTGACAAA | 57626 |
rs376952870 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70101924 | TAATAGTAAACTATG[C/T]AACACAGAAACCTAG | 57626 |
rs376981761 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69984204 | AGGCAGATAGTGAGG[G/T]TACGGATGTCCTTGG | 57626 |
rs376985856 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69926035 | TCAAGTCAGTCTATA[C/T]AGCAAGTTCATTCTC | 57626 |
rs377004132 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70019640 | CCTCTATTTTACAAA[C/T]GATGAAATTGAGCAA | 57626 |
rs377007541 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69821463 | GGGATTACAGGTGTG[C/T]GCCACCATGCTTGGC | 57626 |
rs377019308 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69847123 | ATGCTGCTTGATATT[A/G]TAAATAACTTTTACA | 57626 |
rs377024190 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101187 | ATTTTTCTAAACAAT[A/T]TGAAATAGTACCATA | 57626 |
rs377037600 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098036 | TGAAAATATTAAAGC[C/T]TAGATAAAGCTCTGT | 57626 |
rs377048767 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69961789 | TCGTGAATTTGAACG[C/T]ATAACATATATTGAT | 57626 |
rs377068180 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878199 | CTCCTTGCTATAAAA[G/T]TACTTACAGATTACA | 57626 |
rs377069971 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69750689 | ATGCTGATCATGGGC[C/T]TAACACAATGTAGTG | 57626 |
rs377077361 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69904982 | CTGCAAAACTAACTA[C/T]ATCATGGCTACCCTG | 57626 |
rs377088646 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69957043 | TTCTGAGGATGACGC[A/G]TGCAATAACTCCTGA | 57626 |
rs377096090 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70070679 | TAGAAAGGAAGAATG[C/T]GGGAGAAGAAATAAA | 57626 |
rs377102030 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70055616 | AACAACTTCTTAAGA[A/C]ATAGGTAGAATAATA | 57626 |
rs377110806 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69842283 | TGGGAGAAATATTAG[C/G]AAATTATTTATGCAA | 57626 |
rs377118736 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69973048 | GATTTCCTTCAAGGC[C/T]TAAAGCACAAATGAG | 57626 |
rs377121097 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70052983 | GTGGGAAAAAACAGA[C/T]AAGTACACAATTGCC | 57626 |
rs377131130 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69745465 | CATTTTCACTTTCTT[A/G]ATCTTGTCTTTTGAT | 57626 |
rs377173634 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69861348 | TATAGATACTTTATA[C/T]GTCTATGAACATTTT | 57626 |
rs377198195 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69748874 | TGTCATTACTCTCAA[A/G]ACTTAAATTCCTCTC | 57626 |
rs377199180 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69770349 | CATGAACAAAACTCA[C/T]GCAGAAGCTTTGCTG | 57626 |
rs377199407 | in-del | -/TG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69712759 | ATTTTGTTTGTTTTT[-/TG]TTTTTTTTTTTTGGG | 57626 |
rs377213465 | snp | A/C/G | 3.30602e-05 | 0.00406561 | synonymous-codon | KLHL1 | GRCh38.p7 | 13:69707727 | GTCACCAAGGAGACA[A/C/G]ACCCCAACAGCATCT | 57626 |
rs377221070 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947974 | ACTAAAAGGGAAAAC[C/T]TACATGTTTTTAGTT | 57626 |
rs377223543 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69972512 | GCTGTAAAAATTTAA[A/G]TAATACATCTGTTGA | 57626 |
rs377223663 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70089196 | ATTGCTTCTCTACAT[C/T]TTATCTATTCTCATC | 57626 |
rs377234490 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69948740 | TTCTATTTCTTATTA[G/T]ACACATCATCCCCTA | 57626 |
rs377248172 | in-del | -/AGAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70024365 | TAGATAGAAAGATAG[-/AGAG]TGAGAAAGGGGGAAG | 57626 |
rs377258505 | in-del | -/TAGATAGATAGA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855289 | CACTCGTACTAATTT[-/TAGATAGATAGA]TAGATAGATAGATAG | 57626 |
rs377272374 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69716358 | AGAATATAGAGATGG[G/T]TGGAAAGCTATCTTG | 57626 |
rs377290470 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70016698 | TTGGGCACCATGGAT[A/G]ACCTATTGATGGAAG | 57626 |
rs377303708 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69952875 | TGCTTGTTTATATTT[C/G]CTTGTTTTCCCCCCA | 57626 |
rs377341436 | in-del | -/AAAT | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005176 | GTTACCAAAGAGAGA[-/AAAT]AAACATTTATATCTA | 57626 |
rs377343686 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69919682 | TTACTGGACAAGCAG[G/T]TCACAACAGCCTGAA | 57626 |
rs377356321 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70017077 | GTTCTGCCGCTCAAT[A/G]AAGCTCTTCTCCACT | 57626 |
rs377362177 | in-del | -/TTTT/TTTTCT/TTTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69884934 | GCACTTTTTCTTTTC[-/TTTT/TTTTCT/TTTTT]TTTTTTTTTTTTTTT | 57626 |
rs377372336 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068494 | TATACAGTGGCACAT[A/G]TTTGAGTTTCAGACC | 57626 |
rs377380196 | in-del | -/AAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70031205 | TGCAATTCTATGCAG[-/AAG]GTTTAAGAAGCATCG | 57626 |
rs377380632 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086303 | AAAAAGTAGACCTGG[A/C]TGGGCATGGAGGCTC | 57626 |
rs377389890 | in-del | -/AATA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730481 | CGACTGTTACTTATA[-/AATA]GTGATTAGAAAACAT | 57626 |
rs377401015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726349 | TGTTTTCTAATTAAC[A/G]AAGAGCTCTTTCATC | 57626 |
rs377428978 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69838505 | GAAGGACTAAATTAG[C/T]AAACACAATTAAACT | 57626 |
rs377430097 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69816727 | CCAAAACTTAAACTT[A/G]TTATTTCTACCATTA | 57626 |
rs377448940 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70043680 | CAATATTCTGTAAAG[C/T]AACTAGCTATACAGG | 57626 |
rs377454061 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69792592 | TATGTTCAAACAAAA[A/G]GCATATATAGTAGTT | 57626 |
rs377466112 | in-del | -/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69769684 | AGCCCAGGACTCAGC[-/CA]CACACACAGCTACCC | 57626 |
rs377487390 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70024925 | AGTCTGAAGGACAAT[A/C]CCAGGAATAATAATA | 57626 |
rs377518916 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70019410 | TAAGAGGAAGTTGAG[C/T]ACTTTTTCACCAGCT | 57626 |
rs377519503 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69777167 | TGCCATCATGTAAGA[C/T]GTGCCTTTGCTCCTC | 57626 |
rs377525979 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70007902 | AGTCCTACAGATAAT[C/T]TATAGATAACTAATC | 57626 |
rs377528485 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730371 | CACCCATATTAGGCA[A/G]ATTTGCTGTGTTAAT | 57626 |
rs377528618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989761 | GATTTGACTCTTGGC[A/G]TGGGTGTTGTTAGTG | 57626 |
rs377542805 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69927047 | AGAATGCGGTACTGG[C/T]ATAAAGACACACATA | 57626 |
rs377547738 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69945222 | AAACTCCTGACCTGT[C/G]TTGGCCTCCCAAAGT | 57626 |
rs377565783 | in-del | -/AAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69832647 | GCCAAAGCAAGACTA[-/AAC]AACAACAACAACAAC | 57626 |
rs377568045 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69933989 | GCATGAAATCTGTAG[C/T]GAGATAGTACTGGGT | 57626 |
rs377568187 | snp | A/C | 0.0562307 | 0.157967 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068165 | GCTAACACGGTGAAA[A/C]CCCATCTCTACTAAA | 57626 |
rs377573353 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69963035 | TTTCACTTTACTTAG[A/C]GCCTAACATTTATTT | 57626 |
rs377602076 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69842173 | CAAAAGCACAGGCAA[-/A]CAACAATAAAAAGAC | 57626 |
rs377603658 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70059180 | TTTTTTTTTCCTGAG[A/C]TGGAATCTCACTCTG | 57626 |
rs377634266 | snp | C/T | 8.76309e-05 | 0.00661874 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975831 | ACACACACACACACA[C/T]ACAAAATAATAAAGG | 57626 |
rs377640422 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69832961 | TCAACTCAATATGAA[A/T]CAAAGACTTAAATCT | 57626 |
rs377653781 | in-del | -/AA | 0.424503 | 0.179021 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797663 | CTCTACTAAAAATAC[-/AA]AAAAAAAAAAAAAAA | 57626 |
rs377671459 | in-del | -/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69876663 | ACAAACACACACACA[-/CA]TTGCTATATATTTCC | 57626 |
rs377681849 | snp | A/C | 0.000424463 | 0.014562 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701678 | TCCAGCAAGTAAAAT[A/C]TTTCCAAGTAAAATA | 57626 |
rs377687167 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69721513 | ATTTTTTCTTTACTA[C/T]GGACAATATATCCAA | 57626 |
rs377696244 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105780 | TAGTATTCATAGTAC[C/T]TAACGTTATAATTCT | 57626 |
rs377698240 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70059986 | GGAATTGTAATTTGG[C/T]ATGAGATTTGGGCAG | 57626 |
rs377702192 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70035595 | TGGATCTTTTTATGA[A/C]AGTTTGGAAAGACAT | 57626 |
rs377716482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793940 | CTTAGGAAGAGTTAC[C/T]GCATGTTTCCTATCC | 57626 |
rs377721190 | in-del | -/ATAA | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977362 | ATCAAATGGAAACAA[-/ATAA]GGCAATACAATAATT | 57626 |
rs377724584 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69930570 | ACAAAACTATATCAA[C/T]GCATCCTCAAATGAT | 57626 |
rs377739340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757681 | CATGTTGGCCTGGCA[A/G]TGGCTTACGCCTGTA | 57626 |
rs377742987 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69784233 | CACTGCAAAAACATG[A/C]CAAAATGTAAAGACC | 57626 |
rs377751089 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830577 | AACAATGGACTTAAA[C/T]TATACCCTGGAACAA | 57626 |
rs377751155 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996893 | CCTTTATGAAAAGTT[C/T]TTATTTTATTCATTA | 57626 |
rs377751835 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69813014 | ATGCTGCTATAAAGA[C/T]ACATGCACACATATG | 57626 |
rs377752652 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901343 | CCTAAGTCACCTTTA[C/G]ACTTAACTTTGTTTG | 57626 |
rs386379647 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69819624 | GGTAATGCAAAAAAA[-/A]AAAAAATGTAGAAAT | 57626 |
rs386379648 | in-del | -/ACT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69851106 | AAACATACATATATA[-/ACT]CTTTTATTTTTTATG | 57626 |
rs386379650 | in-del | -/ATTC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69950365 | AGAGTAAAAGCAACA[-/ATTC]TTCCCTTGACTCACA | 57626 |
rs386379651 | in-del | -/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69960127 | TTTTTTTTTTTTTTT[-/TT]TCAGGAAGCTTTTTT | 57626 |
rs386379652 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69997691 | ATTACTTATATATAT[-/TA]AATATAAATACATTG | 57626 |
rs386379654 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70012908 | TTCTGTATAAAAAAA[-/AA]ATAATAATAATAAAT | 57626 |
rs386379655 | in-del | -/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70076388 | AGGAAAGGATAATCT[-/TT]TTTTTTTTTTTTTAA | 57626 |
rs386379656 | in-del | -/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70076400 | TCTTTTTTTTTTTTT[-/TT]TAATGGTTTTGGATC | 57626 |
rs386419879 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69714865 | TCCAAAGGTGCCAGT[-/A]TTACAGGTGTGAGCC | 57626 |
rs386772038 | in-del | CC/GCA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69728662 | GCCAAAAAAAAAAAA[CC/GCA]AAGTGTGGTGACGTA | 57626 |
rs386772039 | multinucleotide-polymorphism | GTG/TTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69729180 | TTATTCACTTTTTTT[GTG/TTT]TGTGTTTTCTTTATT | 57626 |
rs386772040 | multinucleotide-polymorphism | AGCAAAAGCGGAAA/TGCAAAAGCGGAAT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69748412 | AGAAAATTAGGAAAA[AGCAAAAGCGGAAA/TGCAAAAGCGGAAT]CCCCTGATAAAACCA | 57626 |
rs386772041 | in-del | ACT/TCCA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69757791 | TGAAATCTCGTCCCT[ACT/TCCA]AAAAATGCAAAAAAT | 57626 |
rs386772043 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781015 | GTAAGTTTCTTCCAG[CA/TG]TAATATATCAGACCA | 57626 |
rs386772044 | multinucleotide-polymorphism | AG/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781932 | TTTTATTGCTTTTAA[AG/CA]AGATGACATCAATTG | 57626 |
rs386772045 | multinucleotide-polymorphism | AA/CG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69789460 | AAGTTTTCCTTGTAA[AA/CG]TGATGTGAAATAGGG | 57626 |
rs386772046 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69835220 | AAAAGAGAAAAAGGA[CA/TG]CTTCTGACTGTTGGA | 57626 |
rs386772047 | multinucleotide-polymorphism | AAC/GAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69840248 | TTTTTTTTTGAGACA[AAC/GAG]TCTCACTCTGTCACC | 57626 |
rs386772048 | multinucleotide-polymorphism | AG/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69849075 | CATCCGATTTGGGCT[AG/CA]GCACTTTTCATTCCT | 57626 |
rs386772049 | in-del | AACTGC/GT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69851155 | TCTTTTTTAAGTACT[AACTGC/GT]GTTTACTTAAATTTT | 57626 |
rs386772050 | multinucleotide-polymorphism | ATTAAATAATGGGGGCC/GTTAAATAATGGGGGCG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69853239 | ACCCAGTGGGAAGTA[lengthTooLong]TTCACCCTCATGCTG | 57626 |
rs386772051 | multinucleotide-polymorphism | CC/TG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69853656 | TTAAAGTGGTATTCA[CC/TG]AGTGAATGTGATAAT | 57626 |
rs386772052 | multinucleotide-polymorphism | AGGTATT/GGGTATC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69910520 | CCACTACTATGTTTC[AGGTATT/GGGTATC]GGATGGCTGTGGATA | 57626 |
rs386772053 | in-del | GAC/TTTGGGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69919551 | TTTGGGTACATTAAT[GAC/TTTGGGT]ACCAATTTTCTCTCC | 57626 |
rs386772055 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69939642 | GTATTGCCTGTTAAG[CA/TG]TGCATAAAGCCATAA | 57626 |
rs386772056 | multinucleotide-polymorphism | GGT/TGC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69978545 | AGGTTGGGGTGCAGT[GGT/TGC]ACGATCTTGGCTCAC | 57626 |
rs386772057 | multinucleotide-polymorphism | CC/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69990201 | ATGGAAAGACCATTA[CC/TA]AGCCACTATGAAACA | 57626 |
rs386772058 | multinucleotide-polymorphism | AA/GC | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995561 | TGCTGTAAAATTGCT[AA/GC]AAATCTATAATGGAA | 57626 |
rs386772059 | multinucleotide-polymorphism | ACT/TTC | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996098 | TCATGAGGTCAGGAG[ACT/TTC]GAGACCATCCTGGCC | 57626 |
rs386772060 | multinucleotide-polymorphism | AC/GT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70012561 | GCTATTTGAATGGTA[AC/GT]ACCTATTATTAAACA | 57626 |
rs386772062 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70025345 | TAGTTGACTTTGAGG[CA/TG]GAATTATTTTATGCA | 57626 |
rs386772063 | multinucleotide-polymorphism | AATTATGCAGTTGGGT/GATTATGCAGTTGGGC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026892 | TAAAAGTTGTTAGAA[lengthTooLong]TATTTTTCTATGTTT | 57626 |
rs386772064 | in-del | CTGAAAGTGAATGTTGT/TTGAAAGTGAATGTTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027373 | TCCCTTTAGAGCCAG[lengthTooLong]TTTTTTTCCCTTCAT | 57626 |
rs386772065 | in-del | -/AAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70031123 | TGCCAACCAAAAAAA[-/AAC]CCAGATGTTAGCTTT | 57626 |
rs386772066 | multinucleotide-polymorphism | AC/GA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068418 | GTGACACTGATTAAT[AC/GA]ATTATGATTTTATTA | 57626 |
rs386772067 | in-del | AAG/CA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70083404 | CTAACTCCTGGTCTC[AAG/CA]CAATCCTCCCACCTT | 57626 |
rs386772068 | multinucleotide-polymorphism | CCG/GCA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086307 | AGTAGACCTGGCTGG[CCG/GCA]TGGAGGCTCATGCCT | 57626 |
rs386772069 | multinucleotide-polymorphism | ATC/GTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70096602 | CTTTTATTTTTTCCT[ATC/GTT]GAGTTCTTTGAGCTT | 57626 |
rs386772070 | multinucleotide-polymorphism | CGACG/TGACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70104670 | GCTCATTATTAAATA[CGACG/TGACA]TCATTGTTTGGTGAT | 57626 |
rs397699095 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825998 | CTTACAGAAAAAAAA[-/A]GATTTATTTATTTTG | 57626 |
rs397701250 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096656 | AGCTGTTTTTTTTTT[-/T]AAAGAAATCTTAGCA | 57626 |
rs397704121 | in-del | -/AAGA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860752 | AAATTCTATTTAAGA[-/AAGA]TGAACAATAATAGAT | 57626 |
rs397712817 | in-del | -/CA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954819 | ACACACACACACACA[-/CA]TTTTAAACATATATA | 57626 |
rs397729780 | in-del | -/AA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018059 | CTAGCGCAAAAAAAA[-/AA]GTTGAAAATTTATCT | 57626 |
rs397736153 | in-del | -/TA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69997692 | TTACTTATATATATA[-/TA]ATATAAATACATTGA | 57626 |
rs397739676 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69781105 | GACTGCCCAAATCTT[-/T]GCAGGGGGAGACAGT | 57626 |
rs397749917 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70019480 | GCTGATAGTGAGGGG[-/G]CTAGTGGGAGGGCAG | 57626 |
rs397776940 | in-del | -/AAAAT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904170 | TAATAATAGAAAAAT[-/AAAAT]GCATTAAGTTTGGAA | 57626 |
rs397777197 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70000936 | TTACAGAAAAAAAAA[-/A]CAAAAAATAGATGCC | 57626 |
rs397782347 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922462 | CCGAGTTTATAAAAA[-/A]GACTGTTTGCTAATA | 57626 |
rs397784607 | in-del | -/AGTA | 0.391275 | 0.206256 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780999 | TTATTTTAGTAAGTA[-/AGTA]AGTTTCTTCCAGCAT | 57626 |
rs397791110 | in-del | -/AACA | 0.317007 | 0.240853 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925686 | AAATAAACTCTAACA[-/AACA]TTTGAAGTTTTATTG | 57626 |
rs397798632 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69793508 | GTAAGTTTTTTTTTT[-/T]ACATAAATCAAAGGG | 57626 |
rs397804083 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027395 | GAATGTTGTTTTTTT[-/T]CCCTTCATCCATGAG | 57626 |
rs397809674 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69979182 | CAAAAAAAAAATAAA[-/A]TAAGTTCCAGTTCTC | 57626 |
rs397820428 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70045842 | TAAGAGTATCTGCAT[-/T]ATTTCCCAGATTAAC | 57626 |
rs397820650 | in-del | -/ATTC | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950368 | GTAAAAGCAACATTC[-/ATTC]CCTTGACTCACATCG | 57626 |
rs397824335 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70096655 | TAGCTGTTTTTTTTT[-/T]TAAAGAAATCTTAGC | 57626 |
rs397836706 | in-del | -/AAC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69790255 | aaaaaaatattaaac[-/AAC]tctggaaactaaaaa | 57626 |
rs397838440 | in-del | -/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70097898 | TTCTGTTTTTTTTTT[-/TT]CAATTTTAATAGGCT | 57626 |
rs397838446 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70018058 | ACTAGCGCAAAAAAA[-/AA]AGTTGAAAATTTATC | 57626 |
rs397940027 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69764541 | ATTTCTACTAAAAAA[-/A]TGGCACAAAGAAAAA | 57626 |
rs397953868 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69963884 | CAAAAAATAAAAAAA[-/A]CATACACAGCTTTCA | 57626 |
rs397965183 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69794573 | GAGATTAAAAAAAAA[-/A]GAGCTGGGGGAAGGA | 57626 |
rs397975759 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70024404 | AGATTGAGGAAAAAA[-/A]CTCAGGGGACTTGCC | 57626 |
rs398023272 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712273 | TCATTTTTTTTTTTT[-/T]AAGGCGATCTCCTGT | 57626 |
rs398023273 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743838 | AGAAAAAAAAAAAAA[-/A]CAGAAGAAAGAATAA | 57626 |
rs398023274 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885436 | GTTATTTTTTTTTTT[-/T]CTTTACACTTCATTG | 57626 |
rs398023275 | in-del | -/A | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890245 | ACAATTTCCAAAAAA[-/A]GAAAATGTTTGTAAT | 57626 |
rs398023276 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899033 | ATTTTTTTTTTTTTT[-/T]GTGATTCCTCTACAA | 57626 |
rs398023278 | in-del | -/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959674 | TTTTTTTTTTCCCCC[-/C]AAAGGCCTGAACATT | 57626 |
rs398023279 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969064 | TTAGGAGATTTTTTT[-/T]CATTTATTTATTTTG | 57626 |
rs398023280 | in-del | -/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004524 | TCCTGCCATCCCCCT[-/T]GACTAGTCCACGTTT | 57626 |
rs398056523 | in-del | -/TTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022602 | ATTTGTTTTTAAATT[-/TTT]ACTATTTACATGATT | 57626 |
rs398077358 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69799105 | AAAGAAAAAAAAAAA[-/A]AGGTTTACACAGATA | 57626 |
rs398098952 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719588 | GAATACAACCTAAAA[-/A]CACAATTGGAAAAAT | 57626 |
rs398098955 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69841163 | AATCTTTAAACTTTT[-/T]CCCCTTCAATATCAC | 57626 |
rs398098957 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69849737 | AAATCAGAAAAAAAA[-/A]TCTGCTATTTATTGT | 57626 |
rs398098958 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69851084 | ATACTTAGTAGTCAC[-/C]AACTGAAAAACATAC | 57626 |
rs398098959 | in-del | -/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69929134 | TTGTAGAATCATAAG[-/G]CTGCAAAGAACCACA | 57626 |
rs398117508 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69704973 | GTACACTTAGTTGCA[-/A]CAATAGTTCTCAATT | 57626 |
rs398117509 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69992933 | GAGGGAAAAAAAAAA[-/A]CATGTACCTTTCTTA | 57626 |
rs398117510 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060549 | AGACAAAAAAAAAAA[-/A]TGTGGTATATATAGG | 57626 |
rs398117511 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060861 | AAAAGAAAAAAAAAA[-/A]TGTGGTATATATAAA | 57626 |
rs398117512 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086292 | TTTCAAAAAAAAAAA[-/A]GTAGACCTGGCTGGG | 57626 |
rs527249665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736199 | TTAGCAAGAAAGAAA[A/C]AAACAATCCCATTAA | 57626 |
rs527256985 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69966340 | AGAATTACGCTAATT[A/C]TACTCAGCCAGTGCT | 57626 |
rs527259873 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855301 | TTTTAGATAGATAGA[G/T]AGATAGATAGATAGA | 57626 |
rs527260176 | in-del | -/A | 0.0612291 | 0.163907 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844764 | TTTTCTTCTGGGTTT[-/A]TTTATTTATTTATTT | 57626 |
rs527264533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947765 | CAGTGTCAAGCTTCA[A/G]TGCACACAAATTAAG | 57626 |
rs527281594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901603 | AAGTGATGTGTTTAC[A/G]ATCTTACTGTAACAT | 57626 |
rs527312010 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952344 | TATTTTAGACAAATG[A/C]AAAATAGTTTTTACA | 57626 |
rs527326443 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982021 | GAGAATAAAGCGTAC[C/T]GTGTTTTTGCTTGTT | 57626 |
rs527333196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909845 | TTTTTTACTGTTTTT[G/T]CTTGTTTTGTTTTGT | 57626 |
rs527336123 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988264 | AATAATGGCCTACAG[G/T]TCCTTCCATGTTCCT | 57626 |
rs527339746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735497 | TAACATATGCATTTA[A/G]TTAAATGGTTATATA | 57626 |
rs527351240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909102 | ATAAATATATATATA[A/T]CCTATTATATTAATA | 57626 |
rs527364222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69994895 | CATTTTAAGACATTC[A/T]CTGACAAGAAAACCT | 57626 |
rs527381986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69823739 | ACTTTCTAAAACATT[A/G]GCATTTCCACTTCTC | 57626 |
rs527393070 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075610 | ACACACATATATATA[A/G]GACTTACATATATAT | 57626 |
rs527414351 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69882248 | AGGGTTTTTCAGTAC[A/G]TTGAATCTATTTAAA | 57626 |
rs527414941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780990 | ATCCCCAGATTATTT[C/T]AGTAAGTAAGTAAGT | 57626 |
rs527425817 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995925 | AAGAATGTGTCAATT[-/G]AACTATCACCAGGCA | 57626 |
rs527427231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031071 | TCCCTGAATAGACCA[A/G]TAACAGGCTCTGAAA | 57626 |
rs527430316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951795 | TTTATTTTCTGACTG[C/T]GAACATTCATGCCTT | 57626 |
rs527434896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037344 | CATTCTATAAGCACG[C/T]TGAACATATAATTTC | 57626 |
rs527436349 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69792422 | TAGGCAAAAATGTGA[A/G]GAAACTGATACCCTT | 57626 |
rs527437419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008520 | TATGCATGTTTTTAA[A/C]CATTTGATATATACA | 57626 |
rs527443100 | in-del | -/CTT | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779440 | CTTCTTTCCTTTCTC[-/CTT]CTTTCCTTTCCTTTT | 57626 |
rs527452979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757177 | CTTTTTTATCATTTC[C/T]GTGAACCTCCTTGAA | 57626 |
rs527460181 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022992 | TCATGTCTTCCATAT[A/G]CATAACACATGCATA | 57626 |
rs527472620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805439 | GAACACATTTCTATT[A/G]TATGTATTACATGTA | 57626 |
rs527475393 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002443 | TTTTTTTAAATGAAC[A/G]GAGCCTCAAAAGCAT | 57626 |
rs527482590 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69877727 | GATTAGTTATTATAT[G/T]TCAATAGAGGACAGA | 57626 |
rs527491777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971749 | AATTTCCTTAATTAT[A/C]TTATGGTTTATCTTT | 57626 |
rs527498655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842875 | AAAGAATAAAATCAT[A/G]CCATTTATAGCAACA | 57626 |
rs527511057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936611 | AAAAAAAAAAAAAAA[A/G]TGAAGATTGAACATG | 57626 |
rs527512612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763609 | GACCTGAAACCATAA[A/G]TGATAGTAATTGGTA | 57626 |
rs527512758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050413 | TTTGAATTTCTGATA[C/T]GTTCAGTTAAAAAAA | 57626 |
rs527520225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889658 | GCATGGTGATTATGG[A/G]TGATTTAATTTGGAG | 57626 |
rs527522209 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096511 | TGAAAATGTCTATTG[A/T]TATCTTTGCCCATTT | 57626 |
rs527522851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058076 | CTTAAAAATCAGATG[A/C]TAGAAGGAATATGCC | 57626 |
rs527522875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804744 | AACAAACGATAAAAT[C/T]CATATTATATAATAC | 57626 |
rs527527261 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69962613 | GATAAACCTCTTTAA[C/T]TTCTAATTTTGCAAA | 57626 |
rs527529166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723457 | TGTAGAATTATTATG[A/T]GTCAATAACAAAAAA | 57626 |
rs527544266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101752 | TATTTCTTACGATTG[A/T]TTTAGTTTCTCTAAA | 57626 |
rs527554177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69977718 | CATTATATTTTATTG[A/G]ACCTCTTCCTCTTGA | 57626 |
rs527555775 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108051 | GCTGGAGATGCGCGA[A/G]GGAGGGAGGTCTGAG | 57626 |
rs527556059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063961 | GGCTAATTCAAAATT[A/C]ACCAAAACATCAAAA | 57626 |
rs527582960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014741 | GATGAGATAATGTTA[A/G]TGGCTTATAAATTTT | 57626 |
rs527584700 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69982031 | CGTACTGTGTTTTTG[C/T]TTGTTTCTTTACTTT | 57626 |
rs527586940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063286 | TGATTTTATTTCAGG[A/G]AGCCCCTCCACAGAC | 57626 |
rs527588199 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70079739 | AACTAGGTAATATTA[C/T]TCTTTCTCTTTCATG | 57626 |
rs527591967 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102469 | CATCACTGTCAATTT[A/T]AGAAGTCTATTTAAA | 57626 |
rs527603560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803902 | TGGAAAAGTTCCAGA[G/T]AAGAATATAGCCTAG | 57626 |
rs527629773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769537 | TAGAGTCTGTGACTG[A/G]AGTGAGAACATCTAT | 57626 |
rs527630559 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69924715 | TCATCACGTTGTGTA[A/C]AACAAGAAGGAGAGA | 57626 |
rs527634113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776134 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 57626 |
rs527637416 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69944520 | ATCACTGAACGGGGC[C/G]TTAGTCTTGGGGATC | 57626 |
rs527641275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959672 | ACTTTTTTTTTTCCC[C/T]CCAAAGGCCTGAACA | 57626 |
rs527650136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743918 | AAAAGTTTGAAAATT[A/C]TTTTTGGGGAAAGCT | 57626 |
rs527658189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055213 | GAGCTGCAATACATC[C/T]GGCAGCTGACTTATC | 57626 |
rs527663432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918246 | TGTAAATTTTATTTT[A/T]AAATATAATTAAATT | 57626 |
rs527665225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038527 | CATGTCCAAAAACAA[C/T]GTAAAAGAGATTTGT | 57626 |
rs527665300 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69777877 | ATCATTTTATTCTGA[C/G]TATTATAGTGTGCAT | 57626 |
rs527680709 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787327 | ATATAGATCCATGGA[A/G]CAGAACAGAGCCCTC | 57626 |
rs527696767 | in-del | -/AAAG | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783189 | TACATCACCATTATC[-/AAAG]AAAGATCAAAAGTAG | 57626 |
rs527713544 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876608 | CTTTTTTCTTCTACC[A/T]TTTGCTACAGAAAAT | 57626 |
rs527721060 | in-del | -/T | 0.308414 | 0.24308 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096073 | CATATATGTACCATA[-/T]TTTTTTATCCATTTG | 57626 |
rs527722748 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69887140 | TCTAATTCCTTAAGC[A/G]TCCTTTGCAAGCAAA | 57626 |
rs527723840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69917529 | ACAGGAACAAGAAAC[C/T]CTTGGAGGAATGGTT | 57626 |
rs527733563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995664 | TTAAATGTGATCCCT[C/G]AATTGAAGTAAGTAC | 57626 |
rs527733659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002959 | GATACACACATTTAA[A/C]TACTACCTACATACT | 57626 |
rs527753952 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081967 | AGGAGGAGGCTGGTG[G/T]ATTGGATCATGGGGA | 57626 |
rs527771526 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083514 | TAATTTTAGACTAGT[G/T]ATATACTTATTAATT | 57626 |
rs527777274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837506 | TTAGGTACCTAGCTA[C/T]ATAATGTCCGAGAGA | 57626 |
rs527783754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831112 | AGATCAGAGCAGAAC[C/T]AAATAAAATTGAGAA | 57626 |
rs527788831 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69755325 | TGACAAGAGCTTCCT[A/G]AGGCTTCACTAAAAG | 57626 |
rs527812772 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843386 | GCTTAGGTTTTAGAA[A/C]AGTAGACTCATGACA | 57626 |
rs527815834 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837069 | AGGTTTTTTAAGACA[A/C]AATTTTTTTGACAAG | 57626 |
rs527816262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965962 | GTTTATGAAGTTTAG[A/G]GAAAGAAGTCTTCTC | 57626 |
rs527854724 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69978975 | TGAGACCCTGGTTTG[G/T]GGGGCTGGGGGTCAT | 57626 |
rs527855177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943721 | ACACATTAAAATCTG[C/T]TATTAATTTTAAACT | 57626 |
rs527860055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857428 | GTCTCCCCCTAGTGG[A/T]CATATTACTTATTAT | 57626 |
rs527860307 | in-del | -/AC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69711609 | TTCTGAAAATATAAA[-/AC]AATTAATTTCAATAC | 57626 |
rs527866582 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730811 | TCTCAAACTGCTGGA[C/T]TCAAGCAATCCTCTC | 57626 |
rs527877781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904474 | GAGCTGAAGTTGACT[A/G]GTAATACAGTCTTTA | 57626 |
rs527879363 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109104 | ATAACCTTCTAGTAC[A/C]TAAATCATTGTATAC | 57626 |
rs527883146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059299 | AAGTATCTAGGATTA[C/T]AGCACGCATCACTAT | 57626 |
rs527893378 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777647 | CTGAAATGTAATTTT[C/T]CCTTTTATATTTGCC | 57626 |
rs527895627 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736112 | GACAACGCACAGAGC[G/T]GAAGAAAATATTCCC | 57626 |
rs527896299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027623 | ATGTCACCTAACAGA[A/G]GGCATTTTTGAAGCG | 57626 |
rs527910176 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714242 | GTTCTATTTTGACTT[-/A]ACGTCATATTTTATT | 57626 |
rs527916876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064898 | TATGAAACTACCACC[C/T]CATCTTACATTTTAT | 57626 |
rs527918690 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109650 | ACAGCTGGACTGCAA[C/T]CCCTTGTGCCTTGAT | 57626 |
rs527919839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730393 | TGTGTTAATGAGATA[C/T]CCATTTTAAAAACAA | 57626 |
rs527921763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983993 | CCGATCTCTCACTAC[C/T]TAAAGTCAACTAAAA | 57626 |
rs527934864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820264 | TAAGTAACACCAGTC[C/T]CCCATAACAGGGTTC | 57626 |
rs527954963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911360 | AAAGAGTGACATTTT[G/T]GGAATTCTGGTATCA | 57626 |
rs527957471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782570 | CACTGATTGCTAGCA[C/T]AGGAGTCTGAGATCA | 57626 |
rs527970477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826113 | TTTTGCATAGGAGCT[A/G]AAAAAGTCAAACTCA | 57626 |
rs527975702 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713191 | TCAATCTAACAGTTT[C/G]TAGTTTGATTCATAT | 57626 |
rs527976099 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69893706 | AATATATTTTGTACC[C/T]AAGATGCAGGAAAAA | 57626 |
rs527976573 | in-del | -/A | 0.463989 | 0.129263 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963877 | CTGATGGCAAAAAAT[-/A]AAAAAAACATACACA | 57626 |
rs527981417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737125 | CAAAGAAGGCAGTGA[A/G]GGATTGTGCTACCCC | 57626 |
rs527982708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863494 | TATGAAAAAAAAACA[C/T]AAGAAATAAAAAAAT | 57626 |
rs527986034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744427 | ACATCATCCATATGT[A/G]TCTTGTTTTTCTTAA | 57626 |
rs527991578 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69816511 | TGAAAATGATCCACC[C/T]GCCTAGGCCTCCTAA | 57626 |
rs528000989 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70058337 | GTAAAAACCTAAAGC[C/T]TCCACCAAAAAAAAG | 57626 |
rs528001088 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69859483 | TCCAGTAGGGCAGAC[G/T]CTGTGACAGCTCTGG | 57626 |
rs528013711 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977670 | AAACACGTTTTAATC[G/T]TATAGAAACACCTAA | 57626 |
rs528014318 | in-del | -/GATCATAAGA | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060183 | GTGCTTAACATCATT[-/GATCATAAGA]GATCATAAGAGAAAT | 57626 |
rs528024509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787891 | CATTTATGCAGCCAA[A/C]AAACACATGAAAAAA | 57626 |
rs528027986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953399 | GTAATTATGAGCAGC[G/T]CTGCCTCTCATATTA | 57626 |
rs528033358 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69750245 | TAATTTGTAAAAATC[A/G]TCATCGTGTATAAAG | 57626 |
rs528037186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010445 | TCTAAATATAGAATA[C/T]GACTGAAAGAGAGGA | 57626 |
rs528037832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948518 | GGGAATACTTTTTAA[A/G]TAGGGTTCCAATAAG | 57626 |
rs528075235 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69869622 | CTGGTTCTCTGAATA[A/G]TCACTGTGGAATTGC | 57626 |
rs528075545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885101 | GCCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 57626 |
rs528084360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801021 | ACAAGGTGAAGTCGA[A/G]TTACTCTGTGCGTAG | 57626 |
rs528099033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758709 | GAAAAGAACCATCTC[A/G]TAATTTTTTAAGAAA | 57626 |
rs528112426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884243 | AATAATAATACAATT[C/T]GTAAATAATGTCTTT | 57626 |
rs528119985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931645 | CTCTTTGTTGGCTCA[C/T]TAGGTTTTATATTTG | 57626 |
rs528120666 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70052419 | TACCAAAGAAAGAGA[C/T]ATCTGTTTTGATAAT | 57626 |
rs528125625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807194 | GCTGATGTGAGATCC[A/G]GTTGTAATTGGACTG | 57626 |
rs528133442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059818 | ACATGGAGGATTTGA[A/G]ACTTAAAAGGAGGAA | 57626 |
rs528137040 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69950495 | TAGATTTTTTCCACT[C/T]TCACTAATTTCCATG | 57626 |
rs528140976 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972851 | AATTGAAAATTCAAA[C/T]ATCCAATTTTAATAT | 57626 |
rs528143005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851581 | ACATAGCATTTGATA[C/T]ATATTTTTGATGCAT | 57626 |
rs528143310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103628 | AGAGATGTGGGACAT[A/G]CATAGGAAAGATTTT | 57626 |
rs528152154 | in-del | -/CTAA | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098010 | GTAACTATTTACTAG[-/CTAA]CTAAACTTGAAAATA | 57626 |
rs528176849 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69803768 | AGATGGGTCATATAA[A/G]AAGGAATGCAAGTGG | 57626 |
rs528178188 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70097839 | TAAAAATTCAAAAAA[C/G]ATTCAGAGAATTAGT | 57626 |
rs528181993 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70072020 | GGAAGATCAAAGAAA[C/T]CAAAAGCTAGCTTGA | 57626 |
rs528193031 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798169 | ACTCACCTTCACCAA[A/T]GTTATACCTTCAATC | 57626 |
rs528197823 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69833595 | ACTGTATCCAGCAAT[A/C]CCAATACTGGATATC | 57626 |
rs528198154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890989 | TGTGTACAGGTTTAA[C/T]GGTGTTTTCCTGTTT | 57626 |
rs528200503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944385 | GTCTGTACCTGGTTT[C/T]ATTTGGCCTTCGCCC | 57626 |
rs528215714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897805 | TGCAAGCCACCCTGT[C/T]GTCCTTTGGGTCCAC | 57626 |
rs528216135 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813998 | CTGACTTCAAATTAT[A/G]CTATAAGGCTACAGT | 57626 |
rs528216926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771517 | ATAGAAGCTTCAACT[A/G]AGGTCTCTTGTCTGT | 57626 |
rs528217623 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69853168 | GTTTGACTGTGACCC[C/T]ACCCAAATTTCATCT | 57626 |
rs528221757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015988 | AAATTATTTTATTTA[A/G]AGATCAAGAAAAATA | 57626 |
rs528228219 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70022708 | ACGGTGAGGTTGGAT[G/T]AATTTAGCAAAACAT | 57626 |
rs528230832 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079032 | AATAGTTTTAAGACA[C/T]TCAAGCAAGTAATTA | 57626 |
rs528232774 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69767405 | TCTTCTCTTTTAAGA[A/G]ATATCAGTTATCCAG | 57626 |
rs528233938 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69938292 | TTCAAAATAATTTGA[A/T]ATCATTTAAATTTCA | 57626 |
rs528236546 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69748177 | TATCAGAGGTGGCGA[C/T]AGAGCAAAATGCAAA | 57626 |
rs528247517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913435 | GGTCTCTTCCTCATA[C/T]GCAGGCACTTAGGGA | 57626 |
rs528256037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955246 | ACACTTTTTAATATT[A/C]AAGCAGGACATTAAA | 57626 |
rs528264273 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69848534 | ACTGACATAACTACT[A/C]TTCTGGCCAAATTAT | 57626 |
rs528264943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789092 | ACATATCCATCTGTC[C/T]ATACCTATGCCTATA | 57626 |
rs528269180 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69707328 | AACCAATATATTACA[C/G]TTTTATTTTTTGCTT | 57626 |
rs528272739 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708071 | TACAAAAAAGTGTCA[G/T]ATATATAAATAACTA | 57626 |
rs528291630 | in-del | -/TTGT | 0.485887 | 0.0828076 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728409 | CCTTGTAAAAATTGT[-/TTGT]TTGTTTGTTTGTTTG | 57626 |
rs528305161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833353 | AACAAACATATGAAA[A/C]AATGCTCAACATCAC | 57626 |
rs528310651 | snp | C/T | 1.66335e-05 | 0.00288383 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961268 | AAATGAGCTAAAATT[C/T]ATAAGACATCAGAAT | 57626 |
rs528319457 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053587 | AAAAAACAGTGGTAA[G/T]ACATTTCTGTGATAA | 57626 |
rs528325742 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919463 | TAGATATTGCTGATG[C/T]ATGTTTCTTTTTGTT | 57626 |
rs528326388 | snp | A/T | 0.0440515 | 0.141722 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788670 | GTATAATAATAATAA[A/T]AGAAAATATAGTATT | 57626 |
rs528326927 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69791721 | AGCAAGGACAGCATG[-/C]AAAAGAATGAAGTAG | 57626 |
rs528331198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920074 | TAGGCAGCTGTTTTT[C/T]CTTTGGAAAACAATT | 57626 |
rs528343337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926425 | AATATACCAACAAAG[A/C]ACCTGAGTATCTATA | 57626 |
rs528348204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871487 | GAAACTGTTTTTTCC[C/T]TCTCTACCACATGAC | 57626 |
rs528351675 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707451 | ATTTTAGTAATAAAA[G/T]TACACAAGAATGTAT | 57626 |
rs528355032 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085946 | ATGTATATGGTGACA[C/G]ACATTTCATATTGCT | 57626 |
rs528377006 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080267 | CTCTTTTTAAAGACA[-/C]CTGTCAACACTTGGC | 57626 |
rs528382565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921454 | CTTAGTCTAATTAAT[C/T]CAGACTTATAATTAT | 57626 |
rs528389336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925692 | AACTCTAACATTTGA[A/C]GTTTTATTGCCTTAT | 57626 |
rs528390885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832848 | GGAAACAAAAACATA[C/G]AGTGGGGAAAGGACA | 57626 |
rs528393817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003943 | GGACAAGAAGAGATA[C/T]AACAAGGATAAAAAT | 57626 |
rs528409069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085239 | AGAGAGAGAGAGAAC[A/G]GGAAGTGAGGAAAAG | 57626 |
rs528411998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932328 | CTCATTAAAAAAAGC[A/C]AATTATTGATTTTAT | 57626 |
rs528426777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808184 | CAGCAGTGGCTCTTC[C/T]CACTGGGCCCAGGAA | 57626 |
rs528439212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938664 | ACTTTGATATTTTGG[C/T]TGATGAATTATTTGT | 57626 |
rs528439911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023352 | TTTTCTGAAACACTT[A/G]GTAGTGTGTTGACAC | 57626 |
rs528440669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039588 | TTTTTTTTTCTCTGA[G/T]TTTTATTTCTCTGTT | 57626 |
rs528449799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705210 | TATGTCTTGAAGCAC[A/G]TGCATTATTTTTTTC | 57626 |
rs528453350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733212 | AAAAGTTTGGGTTAT[A/T]CAAACACATATGAAA | 57626 |
rs528466673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725743 | TATTGTTGTAGCTTA[G/T]TGAAATCCTGTTCAC | 57626 |
rs528485524 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69848376 | TGTCAATATCAGCCT[A/G]CAGCCTGAAAGAGTA | 57626 |
rs528485804 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779227 | GAATACCTAACTTAC[A/G]AATTCAAAAGGCCAC | 57626 |
rs528489488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060840 | AACAAGAGTGAAACT[G/T]CGTCTCAAAAGAAAA | 57626 |
rs528490576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832698 | ATCACGTCACCCAAC[A/T]TCAAACTGTACAATA | 57626 |
rs528493096 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029257 | TTCACTGGAAATGGC[G/T]GAATATATGGGCAGA | 57626 |
rs528495168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772994 | CAAGAATAATTTCAG[G/T]AAGATCCGAGTGAGA | 57626 |
rs528500726 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976096 | CCTGAAATCTCACAG[A/T]AATAGTAAATTATTT | 57626 |
rs528524685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707128 | ATTTTTAAAAGGTTA[A/G]TTTCTGTTTATGGCT | 57626 |
rs528525721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821770 | TACTCTCCATTCCCC[C/T]GTTTTTACTTTATAC | 57626 |
rs528528524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905590 | AAGCCTTGAATTCCT[A/G]CCAACTGCATAAGAT | 57626 |
rs528528774 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732677 | TTTTTTTCCTGTGAG[G/T]GTCACCCCATCCTTT | 57626 |
rs528529974 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984979 | AGCCAGGCATGGTGG[C/T]GGGCGCCTGTAATAC | 57626 |
rs528531457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066818 | TCCATGTTTTACCTT[C/T]GATGAAAGTGGCCAA | 57626 |
rs528536288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69992264 | TGCCTACTCTCAGGG[A/C]TGATATTCTAGGACT | 57626 |
rs528537361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979918 | AAAGAATTGTCTTCA[A/C]ATCTTAACTTCAGTT | 57626 |
rs528540934 | in-del | -/A | 0.0418186 | 0.138422 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860855 | TAGAATTACATATTT[-/A]AAAAAAAACATACTA | 57626 |
rs528542182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866279 | CAGGTCTTTTCAGGT[C/T]GGCTTATTGAATTCA | 57626 |
rs528559673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073507 | TCACATGTGTACATA[G/T]GTAACAAGCCTGCAC | 57626 |
rs528571695 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066318 | CTTTTTTAAAAATCA[A/G]TATGAAGCAAGTTTA | 57626 |
rs528572806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998499 | AGAATATGTACATCC[A/G]CATTCCATCATTACA | 57626 |
rs528586910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991738 | CAGAAGTGCAAAGAG[A/G]AGCATTCCTACTGAA | 57626 |
rs528595761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079976 | CACACCAGGATGTGA[C/T]GGTGAATCCCATAGT | 57626 |
rs528596078 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783520 | AGGCTTGAGAACTAC[A/G]TGAAGAATGCAGAAG | 57626 |
rs528604132 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827427 | TTTAGCAGGCCTTTT[-/A]AAAAAAGTCATTCTT | 57626 |
rs528608787 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072852 | AGGATCATACTAATG[G/T]ATTAAGTGTGAGAAA | 57626 |
rs528613762 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701029 | AAACAATCCTTTGTG[C/T]TTGCCAGTTTCAGAT | 57626 |
rs528623679 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028864 | TACCTGTAGGCTCAA[C/T]TACTTACAAGATTGA | 57626 |
rs528631286 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69830083 | AAAAACTACCATGAT[A/C]AAAAGAATAGTACCT | 57626 |
rs528631384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034704 | TTTTGAGGAAGAGGG[A/G]AAGTCGCAATCATTT | 57626 |
rs528644506 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949835 | TTAACAGTTAACAAT[A/G]ACATTTAAATTTTAC | 57626 |
rs528666415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047679 | ACGGTGCTTTAAACT[C/T]GCAGCTAAATACACA | 57626 |
rs528681109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796017 | TGGGTTGCACTACTT[C/T]GGCCTTTCCATGTTA | 57626 |
rs528688584 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933508 | AACCATGATCACAAA[A/C]CACATTGATATAGTT | 57626 |
rs528688651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927495 | AAAATTTAAGAAAAG[G/T]TTTGCAAATCATATA | 57626 |
rs528691806 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70050749 | TAATTGTTACCTATC[A/G]TAACAAAAATATAAC | 57626 |
rs528692392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894374 | ATCTGGTCTAATAAG[C/T]GCTAGCTCCAAAATT | 57626 |
rs528693810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880016 | AAAGAACCTTCAAAA[C/T]TGATTAATTCAGGAT | 57626 |
rs528695696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887148 | CTTAAGCGTCCTTTG[A/C]AAGCAAAGTTTTGAG | 57626 |
rs528699935 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975383 | TTTATTTTTGAACAC[G/T]TTATAATTGTTTTGT | 57626 |
rs528705684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054952 | ACCTCAAAAGGGCAA[A/G]TCTAAGTTATTGGCC | 57626 |
rs528715440 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720651 | GTAACCAGAAAAGGT[A/C]TCACTGAAACCTTTT | 57626 |
rs528715879 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69913697 | GATTGCTTGTTCAAT[G/T]AAATTCAATTACAAA | 57626 |
rs528717956 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802285 | TAAGTATTTGGGTTG[G/T]TTCCAAGTCTTTGCT | 57626 |
rs528718443 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760377 | ATTATTATTTTGAGA[C/T]GGAATTTCACTCGTT | 57626 |
rs528722730 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70014037 | GGACAGAGAAAATAT[A/G]TTCAATTTTATGTGG | 57626 |
rs528736797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094208 | GGCAGCATGCACCTG[C/T]AGTCGCAGCTACTCG | 57626 |
rs528738511 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847033 | CTTTCTGTAAAAATT[A/T]TCTAATGTGTCAAGA | 57626 |
rs528745598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099518 | TCTGTAAAGTAAGTA[A/T]AATGGATGACTCCTT | 57626 |
rs528749358 | in-del | -/TAG | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014781 | TCTAGGGATGAAACA[-/TAG]TAGACTTAAACAGAT | 57626 |
rs528750629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105562 | ATCAGTTTTAATAAA[A/G]TAGTAACAGATAAAT | 57626 |
rs528768052 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69723926 | CACTACAACCTCTGC[A/C]TCCCGGGTTCAAGTG | 57626 |
rs528769999 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939747 | CCCCTCTCCTCATAC[C/T]TCACCCTACACATCT | 57626 |
rs528778786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808782 | AAAAAAACTCAATAA[A/G]ATCTGAGAGAAAGTT | 57626 |
rs528819335 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69933493 | TGTCGGGTATTTTAA[A/G]ACCATGATCACAAAC | 57626 |
rs528835429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015936 | ATTTCATCATTTCAC[A/T]TTGACTACATTTCTA | 57626 |
rs528848036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799778 | GCCTTTTCTATCTTC[C/T]AGAACAAGGGTCCCC | 57626 |
rs528856106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102981 | TACAGACAAACAAAA[C/T]CAACACAGATATTCA | 57626 |
rs528860396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771346 | TTTTTCATCTATTAT[A/G]TTTAAAGTTGGCTTA | 57626 |
rs528862105 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69804977 | TATTTTTTCAATGTT[C/T]TATAGTGTAAGCATT | 57626 |
rs528866106 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70064639 | GAGACTATTGCCTAC[C/T]GTTGTAGTTGTAGTG | 57626 |
rs528866435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897104 | TTGAAAGGATACCTG[A/C]TAATTTATTTAAAAA | 57626 |
rs528869242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718363 | AAAAATTTACTACTC[C/T]CTGGCTTTTTCCTTT | 57626 |
rs528872213 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69785147 | TCCGCCCGCCTTGGC[C/T]TCCCAAAGTGCTGGG | 57626 |
rs528882680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972671 | TATTTCCAACTCAAG[A/C]CTAAGTATATTAGTT | 57626 |
rs528883489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051973 | TTTGTCAAACTCTAT[C/T]AAGATACCTTTTATA | 57626 |
rs528885292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059720 | TGACTCACAGTTCCA[C/T]AGGCTATACAGGAAG | 57626 |
rs528890776 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978672 | TTGTATTTTTAGTGG[A/T]GACGGGGTTTCACCA | 57626 |
rs528894081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097168 | AAAATCTTAACATGA[C/T]ATTTTGCAACCATTC | 57626 |
rs528897621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890532 | AATTGTCCTATTTTT[A/G]AAGCAACATCTGCCT | 57626 |
rs528901663 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765819 | CAGAGAAGGAAGAAG[C/T]GAGAAGACCTCTGAT | 57626 |
rs528907128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805737 | TGTTGAGAGATATTT[A/G]TTGAATGAATGGAAG | 57626 |
rs528914975 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106138 | TCTATTCTTTTTGGT[A/T]CTTAATCAAATTTAT | 57626 |
rs528922751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059150 | TGGGAATGGACAAAT[A/C]TTTCTTCTTTTTTTT | 57626 |
rs528929741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983898 | AATCTATGCATTTAC[A/G]GCTGATTTTTGACAA | 57626 |
rs528940202 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69913448 | TACGCAGGCACTTAG[A/G]GACCTCTGGGTCTGG | 57626 |
rs528941884 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108949 | GGGCCAGAGGCGTAC[A/G]GTAGAAATTTGAAGA | 57626 |
rs528943559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850214 | TTTCCCATTACTCTT[A/C]TTCCTGTAATTGACT | 57626 |
rs528953151 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903225 | GCAATGAAGCCAAAC[A/C]ATTTCCTACTGCTGG | 57626 |
rs528971233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021545 | AAGCATGATTGCTGA[A/C]TCTCATGGCAAACGT | 57626 |
rs528975233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69742375 | AGGACACTCAGTAAC[C/T]TGACTTTAAAGATGT | 57626 |
rs528977144 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943683 | GTTATAAAAATAAAG[A/T]TAAAATAGAGAAAAT | 57626 |
rs529001519 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028366 | ATATAGACAGAGGTA[C/T]GTCTTGAAGTTAATT | 57626 |
rs529008347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730312 | GTTTTCATTACAAAA[G/T]AATGTAAAAAGTGAA | 57626 |
rs529011319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012686 | GAGGCTGAGGCGGGT[A/G]GATCACGAGGTCAGG | 57626 |
rs529026176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948770 | ATTAACAAATGCACA[G/T]AGTATCCATCTTTCA | 57626 |
rs529030535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794306 | TGATTGTTTTGATAA[A/G]ACACAAAAACGTATC | 57626 |
rs529031568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085126 | ATGGATATATGTATG[G/T]GCATGTATGTATGAA | 57626 |
rs529035533 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744758 | TATAATTTAAAAAAT[A/T]ATTTAAAGTTGTTAT | 57626 |
rs529049609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832789 | ACAGAATAGAAAACC[C/G]AGCAAGAGAGCCAAA | 57626 |
rs529052163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752592 | TTCCATGTAGCTAAG[A/C]GTTGTTTTCTTTTAA | 57626 |
rs529054935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039529 | TGCTCATCTTTTTAA[C/T]AATCTTTTTCAAACG | 57626 |
rs529077749 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832137 | TAAAGGGCACCAAAA[C/T]TGGTAAAAAGGAAGT | 57626 |
rs529086367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918356 | CATTACGAAGAGTGA[C/T]TTTTTTATTAAATAC | 57626 |
rs529090122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045589 | CAACACACACACACA[C/G]ACACAAGGAATCCTC | 57626 |
rs529096572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003734 | AAATTTTGTACTACA[C/T]AACACATGGAAAAGA | 57626 |
rs529096800 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69745318 | CTTATTATTAATTAT[A/G]TCATTTTATCAATTT | 57626 |
rs529117913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925621 | CTATCTGAAATTATA[C/T]ATTAATTTGCAGAAG | 57626 |
rs529119610 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751988 | TCAAAATTACAACCT[G/T]GCAATGTGACCTTGG | 57626 |
rs529123828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967003 | TATTTTATTTATCCA[C/G]TCATCAATTGATGAA | 57626 |
rs529124140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097785 | GTGATGTAAAAACTC[A/G]GAAGAGTTCCCCTGA | 57626 |
rs529129030 | in-del | -/AGAAT | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923164 | AATGGTAAAACAGAA[-/AGAAT]AGTAGTAAAGACTGT | 57626 |
rs529131779 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010307 | GAAGATCAATCAAAA[C/G]CCTGTTGTAAAAGAC | 57626 |
rs529132180 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70064878 | TTTTGACTAATGTGT[A/C]CATGTATGAAACTAC | 57626 |
rs529140004 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044924 | CTGTTTCCAGTATTG[A/G]CTATGACTCACAGAA | 57626 |
rs529142144 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69823943 | AAATTTTGCTCTCAG[A/T]ATTAAGTCACCTTTT | 57626 |
rs529144135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713344 | TAATAAAAATGGTAT[C/T]AGCCGTCATTTCTTT | 57626 |
rs529167633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009745 | TATTCATTAATCCAT[C/T]CATTTGTCAAATACA | 57626 |
rs529180911 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930919 | ACTACATATAAAAAG[A/C]CCTGATTTTAACTTC | 57626 |
rs529184127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931579 | TAATCTTCAATCATA[A/G]GAAAATATAACACAT | 57626 |
rs529193227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712457 | CCTTTCCTCACTCCT[C/T]TTTGGTTTCTCCTTT | 57626 |
rs529202297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016420 | GGGCCCAGGAAGACC[C/T]CCTGTCCCCGTAGGC | 57626 |
rs529219750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944515 | AGTTCATCACTGAAC[A/G]GGGCGTTAGTCTTGG | 57626 |
rs529241075 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70015791 | TTTATGATGGGTTTA[C/T]TGGACATAATCCCAT | 57626 |
rs529241434 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966606 | TATTTCATTTCTTTT[C/G]TTTTTTCCTTTTTAT | 57626 |
rs529242127 | in-del | -/T | 0.189016 | 0.242448 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886379 | AAGTTTTGCACCAGT[-/T]TTTTTTTTTGTTTGT | 57626 |
rs529245935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757828 | TTGGCGTGGTGGCAG[C/G]TGCCTGTAATCCCAG | 57626 |
rs529250633 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858204 | TGTGGAAGAAAAACA[A/T]CTCCATCCACTACTG | 57626 |
rs529257448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69949686 | TCTTCTATGTGGGAA[A/T]TTTGTCTATTCTCCA | 57626 |
rs529267861 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70088613 | ACTTGAGCCCAGGAG[G/T]TGGACGTTATAGTCA | 57626 |
rs529268306 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039931 | TTTGAACTTTAAAAA[A/T]ATATATATTTTTTGA | 57626 |
rs529284118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865707 | TTTAAAATTTCTTGG[A/T]GACACAGGGAGTAAG | 57626 |
rs529291077 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70062077 | TTTTGTATTCCTTAA[C/T]CAGCCTCTCCCCATC | 57626 |
rs529291859 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69881076 | TTCTTTGTCTAGGTA[C/T]GTAAATGCATGTTTC | 57626 |
rs529312656 | snp | C/G | | | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700813 | TCCAACTTAATGGAT[C/G]ATATGTTTTTCTTTT | 57626 |
rs529315261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025903 | CATTCTCAGTGGAAG[C/T]GCTAGAGCTAATAAA | 57626 |
rs529339519 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69737024 | TGACTAGGTGGTTGG[C/T]GCAACCCACGGAAAG | 57626 |
rs529340587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882637 | CCTTCAGAAACTAGA[A/G]GCTGTTAAGATGAAA | 57626 |
rs529352466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984518 | AGCCAGCTTCTTTGA[C/G]CTAGGTAAATGTCAC | 57626 |
rs529355871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998078 | AAGAAAAAGGCACAA[A/G]TTTTGATAGGTCCTT | 57626 |
rs529362421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783079 | ACGGTCTGGAGTGGA[C/T]CTCTAGCAAATTCCA | 57626 |
rs529363333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737783 | CAGCTGTAGTATCAC[A/G]CATCAGTGGTCTCAG | 57626 |
rs529364160 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826875 | AAGATTTTTATTTTA[A/G]TAAGAATATATTAAT | 57626 |
rs529370961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865130 | TTTGTAGAGATGGGT[A/G]CTTGCTACATTGCTC | 57626 |
rs529373268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997495 | CCACGGGAAACCACC[A/G]CTTTCCTCTGTTTCT | 57626 |
rs529377867 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69841663 | CTAAACACAATCTCT[C/T]TCAAATTACCAAAGT | 57626 |
rs529379789 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69739855 | ACTTCCCAGGGGATA[A/G]TAGACAATATCTGGA | 57626 |
rs529380321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707370 | AATTCAGATTCTGTT[C/T]CTTGTTGTGGAAAAT | 57626 |
rs529381263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072229 | TCCTGAAGGACACAA[C/T]TGACCAAAACTCACC | 57626 |
rs529396255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033557 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 57626 |
rs529402219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782730 | GTAGGCTCCACCTCT[C/G]GGGGCAGGGCACAGA | 57626 |
rs529403250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085905 | AAGAACACTGAATAA[A/C]GAGGATTATGTGAGT | 57626 |
rs529410446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871438 | AATTTCTCTAGTAAG[C/T]GATTGCTCCACAGCA | 57626 |
rs529413540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69954174 | AATGAACACTGGGCT[G/T]CCCACATCACACTGA | 57626 |
rs529416803 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939356 | ATATATATATATATA[C/T]ATATATATATATATA | 57626 |
rs529422301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078538 | CTTAGTGAAGGGTAT[G/T]GGCTTGGCAGTCACA | 57626 |
rs529425859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788606 | ACATGGCACATGTAT[A/G]CATATGTAACAAACC | 57626 |
rs529426186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039906 | TGGGCCTCCCAAACT[A/G]CTTGGATTATTTGAA | 57626 |
rs529434403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054265 | TTATAAGAAATATCT[A/G]TCTTGGTAAACTTTA | 57626 |
rs529467227 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69799463 | CTCAATACATGACAG[A/G]ATTTTTAACCTTTAC | 57626 |
rs529468079 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011136 | TAAAATGTCCAAGAA[A/C]AAAGTCCAGAGAAAA | 57626 |
rs529470300 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69945803 | ATCTCTCCTATGATT[C/T]AGCCATTCTGCTCCT | 57626 |
rs529472434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974128 | TACTTAAGTTTATCA[C/T]TTAACAGTGTAAAGA | 57626 |
rs529482474 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69947311 | GTTCAGGCAAATGGT[A/G]TATAATTGACCATTT | 57626 |
rs529485748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782119 | TGTGTTCTTTTTCTG[C/T]TTTAAGCTCTCTCTT | 57626 |
rs529494348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932501 | AAATGATTGAAATCA[C/T]TAAATATTTAGGCAC | 57626 |
rs529507011 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719694 | AAACGTGTTGGAAAT[A/G]TATTACTTTGCAGGG | 57626 |
rs529510627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766312 | CATTATTATACATTA[A/G]CTGTTTCAAATATGC | 57626 |
rs529520802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980227 | AGTTAGTTACTTCCT[C/G]AAGGAAATATTTACT | 57626 |
rs529542761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852454 | GATTTTCTGATTTCA[A/G]TAATGACGTGGACCT | 57626 |
rs529546164 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69903631 | CCCTTGTTCACATTC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 57626 |
rs529547755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099474 | AGAAGAAGGCAACAA[C/G]ACTCAATGTACATAT | 57626 |
rs529558284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017070 | GAGAACTGTTCTGCC[A/G]CTCAATGAAGCTCTT | 57626 |
rs529563735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898715 | GGGGAATGTGGAAAA[C/G]TGTGAACCTATCCAA | 57626 |
rs529594414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022518 | TATATATACTTAATA[A/C]AATATGGTGATCAAA | 57626 |
rs529599605 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747097 | GTACTCTTTCCATCT[C/T]TTTCACATCTTGTTC | 57626 |
rs529601714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955925 | TTGATATATATATTT[A/C]TATATATTTGATATA | 57626 |
rs529633029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858851 | CAGAAAGAAAGAATA[C/T]GTCCAGAGGAATGAA | 57626 |
rs529652955 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70003893 | TGAAGAACTGGATCA[C/T]ATCAAATTTAATATA | 57626 |
rs529656828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047485 | AGAAAACTTTAGTGG[C/T]CATGTTCTTTAGAGA | 57626 |
rs529658992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754089 | TCAAGCAATCCACCT[C/G]CCTCAGCCTCCCAAA | 57626 |
rs529659331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962073 | TGGGGAGACTTGACA[C/T]AATTTTCATATAAAT | 57626 |
rs529672760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040723 | GTTTTAGATTCACCC[A/T]CCTTGAATTTGTGGG | 57626 |
rs529692556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834070 | ACAATACAATGGACT[C/T]TGGGGACTTGAGGGG | 57626 |
rs529693676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046846 | ACCCCACCAAGTACC[A/G]AAGCTGCAATCAGGA | 57626 |
rs529695173 | in-del | -/ATAT | 0.145978 | 0.227331 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889043 | TATGTTGCATAGGTC[-/ATAT]ATATATATATATATA | 57626 |
rs529697694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998628 | CTTCTACCTCAATCA[A/G]TAACTAGGACCTTAA | 57626 |
rs529723371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879838 | AGAAGATGGCAATCA[A/C]GCTGATTCTCAAAGT | 57626 |
rs529725497 | in-del | -/T | 0.250168 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981941 | TATTAAAATAATAAC[-/T]TTTTTTTCAGAAATA | 57626 |
rs529735540 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753717 | TCTAGGCAATTGTCC[C/T]ACTTGAAGATTATTC | 57626 |
rs529739896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839694 | GGAATTTAAAAGTTG[C/T]GTATTAGGCAAAGTA | 57626 |
rs529741411 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086447 | AATTAGCCTGGCGGT[C/G]GTGGGCACCTGTAAT | 57626 |
rs529744255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087185 | CTCTTAGTGGAATAG[A/G]AAAAGTCAGGTTTCA | 57626 |
rs529754465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802219 | TTTTATGGCTGCATA[C/G]TATTCCATGGTGTAT | 57626 |
rs529757374 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69876326 | ATGAAGAGTCCGTAT[A/G]TCACTGGTATCTGAT | 57626 |
rs529766816 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879023 | ATCAAACACCACATG[C/T]TCTCATTCATAGGTG | 57626 |
rs529768881 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926566 | CTATCAAAATCCTAG[A/C]TGGCTATTTGCAGAA | 57626 |
rs529774426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789244 | TTTCAGAATTTTTTT[A/T]AAATTACTTTTTTAA | 57626 |
rs529778950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795926 | AATTAGGTTCAAAGA[C/T]ATAGATGTGCTTAAT | 57626 |
rs529792486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927402 | AAGAAAAATGGATAA[A/G]TCTGACAACATTGAA | 57626 |
rs529795690 | in-del | -/CTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69997278 | CAAATTTTATTTTTT[-/CTT]TTTTATTTTTAATTA | 57626 |
rs529804547 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933055 | CATTTTTACTTAGTT[C/T]TTTTCAACATTAAAC | 57626 |
rs529810347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079256 | CCTAAGAATCTTTTT[A/G]ATAATCCCTATTCCT | 57626 |
rs529812814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820353 | TACTAACTCTTCAGT[A/C]CACAAGTCATTACTT | 57626 |
rs529827558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093880 | ATTATACACTTTATC[A/G]AGATCATATGCATAT | 57626 |
rs529852529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872586 | GATGCACCCTCTCCC[C/T]TCTCTATCACCCCAT | 57626 |
rs529856347 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852674 | CAAAGCCCAACATAC[C/T]TCTTTTGATCAACAT | 57626 |
rs529860501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779970 | CACCACACCCAACTA[A/G]TTTTCGTATTTTTAG | 57626 |
rs529878915 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074795 | ACAATAAAGCAATAA[A/C]TTAAAATAAAAAACA | 57626 |
rs529880269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740627 | TAAAAATCTGTTAAG[A/T]GGGTAGATCTCATGT | 57626 |
rs529881544 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70035764 | TAACTTTTCATTTTG[A/C]GAGAATCAAATGAGA | 57626 |
rs529883031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69986656 | ATAAGATACGCTGAT[A/G]TTTGGTAAGAAATTT | 57626 |
rs529885049 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70021237 | TTTCCATAGTTTTGC[C/T]TTTTCCAGAATGTCA | 57626 |
rs529885730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899864 | GTAGACAGAATAATT[C/T]GTACTATGAACAATA | 57626 |
rs529886059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726453 | AACGTGCTTTACAGG[A/G]CAGTGAGTGGGATTT | 57626 |
rs529889970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023988 | ATTAGCCTCCTCAAG[C/G]ATTTTCTCTTGATGT | 57626 |
rs529905649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867120 | GCCTCAGAAGCATTA[C/T]TTGATTAAAATCCAG | 57626 |
rs529913384 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70005610 | TATATGTTAATGTAT[C/T]TAGTATTAATCATAT | 57626 |
rs529913673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074257 | GAGTAGGACTGTTTC[A/G]TGTAGAAGTACTACC | 57626 |
rs529919140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785174 | TGGGATTACAGGCGT[C/G]AGCCACCGCGCCCGG | 57626 |
rs529932481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733612 | ATATATTAAAGATGT[C/T]TGATCACATCAGTTC | 57626 |
rs529944453 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70001851 | ATTTTCTATCAGAAA[C/G]TAGAGAAAGCATTAT | 57626 |
rs529946966 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907314 | AACTCAAATACCACA[A/T]CCAACACTGACATTG | 57626 |
rs529951007 | in-del | -/TACTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70002582 | CCAAAATTTAACTTA[-/TACTT]TAATCTACAAATCCA | 57626 |
rs529951480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873378 | ATATTTCAACAATTC[C/T]ATTCTCTCTCTCTCA | 57626 |
rs529956323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815426 | GATGCAGCTGTAGGC[C/T]ATTATCCTAAGCAAA | 57626 |
rs529971654 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108349 | ATGCCAGAAGAGGTG[A/G]TTTTATATAGTCAGT | 57626 |
rs529974625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779411 | CCCTCTTCCCTCCTT[C/T]CCTTCCCTTTTTCCT | 57626 |
rs529981323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956829 | TGCTTATTTGAAATA[C/T]GAAATATGTAATTTT | 57626 |
rs529989557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888215 | ATCAAGGCAGAGCCC[C/T]TATGACCCAAATACC | 57626 |
rs529992978 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69852856 | TCTTTACTGAGAAAA[A/T]ACTTCAGGAATAAAT | 57626 |
rs529995023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739741 | GAAAATAATTTAAAA[G/T]ATCAGACTAGAAGCT | 57626 |
rs529995057 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69827760 | AAAAAAAAGTTATTC[C/T]TAGCACATCTCATCA | 57626 |
rs530013149 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69732047 | CAAAATAAGGTGGTT[A/T]TAAAGGTGATTGGAA | 57626 |
rs530015425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080805 | GTTTTGCCATGTTGG[G/T]CAGGCTGTTCATTTG | 57626 |
rs530023647 | in-del | -/AA | 0.137527 | 0.223271 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836854 | TGCTCAAGAAACTGC[-/AA]AAAAAAAATGCAATA | 57626 |
rs530035166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056379 | GAGACAGACCCCAAT[A/G]TAATAATAGCTGGTG | 57626 |
rs530037731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921151 | TAATAGCATTTTCTT[C/T]AGAATAAACTAAAAA | 57626 |
rs530038384 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69784229 | CAGCCACTGCAAAAA[C/T]ATGCCAAAATGTAAA | 57626 |
rs530039691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914286 | TCACATTATACATTT[A/C]TACTGGAGTTTTACT | 57626 |
rs530069603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810066 | TAGACCTAAGAAAAG[A/C]CTTTGACAGCCACAA | 57626 |
rs530073207 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094725 | AATGTGGCTTCCTTA[G/T]CCGGCCAAGTGTTTC | 57626 |
rs530074845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887402 | AGCAGCTTTTTCATT[C/T]TTTACAACAGGGCCA | 57626 |
rs530075106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101337 | TATTTATATATAAGT[A/G]CATCGTAGTATAAAC | 57626 |
rs530082593 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70094187 | AACTTTATGTAAGCC[A/G]GATGTGGCAGCATGC | 57626 |
rs530084668 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70072819 | AAAAAACTTTTATTT[-/A]AAAAAAAAACTACAC | 57626 |
rs530090657 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715555 | AGACGGAATCTCGCT[C/G]TGTTGCCCAGGCTGG | 57626 |
rs530101617 | in-del | -/A | 0.173907 | 0.238138 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060852 | ACTTCGTCTCAAAAG[-/A]AAAAAAAAATGTGGT | 57626 |
rs530106588 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981358 | TCACTAAGAGAGTAA[C/T]GAAAACGGCAAAATA | 57626 |
rs530110026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900290 | GAACGTAATATTCAT[C/T]GGTCTCACCATATAG | 57626 |
rs530110428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048567 | GAAAGCAATTTTTCC[A/G]CAGATGGCAGGCTAG | 57626 |
rs530116913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767765 | TTCAGTAGGCTTCTA[A/C]TTCAATTTACTACCT | 57626 |
rs530119091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774821 | ATGTGTTATCTTTTA[C/T]TGTACAAGTCAGCTT | 57626 |
rs530126251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761168 | ATAAGAATCTGGCAG[C/T]ATAATGAACCAGAAT | 57626 |
rs530132386 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734808 | GAATATTAAAGGTAC[C/T]ATATATAATAGTGTC | 57626 |
rs530136367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802769 | AAAGGACAGGAATTG[C/T]TCAGTCAGGGAGCTC | 57626 |
rs530157459 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69919540 | GAAAAATGTACTTTG[G/T]GTACATTAATGACAC | 57626 |
rs530163738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721702 | ATTTTAAATCCTGGG[A/T]ATGTTTTTCTAAAGC | 57626 |
rs530173602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061896 | TAATGATCAAATCAG[A/G]GTCATCAGCATGTAT | 57626 |
rs530173753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106501 | ATAAACTAGAAATAA[A/G]TATTGAGCTGTTTAC | 57626 |
rs530181530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774452 | TCTTTAGTACAATTT[C/G]GCAAAATAATGGAAA | 57626 |
rs530207740 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830044 | ACAATAATACAGTGG[A/G]AAAAAAAAAGAAGGT | 57626 |
rs530209098 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916127 | AGAAATAGGAACACT[G/T]TTACACTGTTGGTGG | 57626 |
rs530209381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018801 | AATCAATGGTTAGAA[A/C]AAAGTTACTTCTCAA | 57626 |
rs530210272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933783 | GGTAGCACCGGACAG[A/G]AAACAGAGAAGGGGG | 57626 |
rs530210890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791473 | AAGGGACCCAGAATA[C/T]CCAAAAATTCTTAAA | 57626 |
rs530214539 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69901462 | GCAGACAATTTGAAA[G/T]AAGTGTCTATGATAT | 57626 |
rs530219848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875140 | ACAATTGAGATTGGG[A/G]GGAAAATTACACCAT | 57626 |
rs530251647 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69881284 | TAATATATGACCATA[A/G]ATCCCACTTCTACAC | 57626 |
rs530252022 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024404 | GAGATTGAGGAAAAA[A/T]CTCAGGGGACTTGCC | 57626 |
rs530255786 | in-del | -/ATG | 0.0228947 | 0.104514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802150 | GTTAGTTTGCTGAGA[-/ATG]ATGATGGTTTCCAGC | 57626 |
rs530256341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964581 | TCATATTTTCACCAA[A/G]TTAACTCTCTGATAC | 57626 |
rs530257092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881787 | CTAACTACTGTTAAA[C/T]CATAACTCTCTACTA | 57626 |
rs530266018 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69792001 | GTCAGGAGAAATAGC[A/G]AATGCATGCTGGGCT | 57626 |
rs530269494 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915530 | GGCGCTGGGAAAACC[A/G]GCTAGCCATATGTAG | 57626 |
rs530284039 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976432 | ACTTTATGATTTTGG[A/G]AAGTCCATGATACTT | 57626 |
rs530290829 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995419 | AGAAAATGTATAGAT[C/G]TTTTGTGTAGAAATC | 57626 |
rs530293088 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710264 | TTTAAAAAATACTAA[A/C]CTGCAATCAGAAATA | 57626 |
rs530294098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036774 | TATTCATCCCACTTT[G/T]CTTGTTTCCTTTTAC | 57626 |
rs530296000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790964 | CTGATAAAAACATCT[A/G]TTTTTAAAAAAGGAG | 57626 |
rs530297650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798246 | TTAAGCACTGATGAT[A/C]TATTTTACCTGTAAT | 57626 |
rs530306123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095175 | GTATCGGTTATAGAT[C/T]TAAGTGAAATTTGGG | 57626 |
rs530311206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785873 | ATCAGAGAATACTAC[A/G]AACACATCTACGCAA | 57626 |
rs530311951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000018 | GAACGGCTTGCTGCC[A/G]TCCTTATAATAATGT | 57626 |
rs530322268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755574 | TTTCAAATATGATAG[A/T]TCTGAATTAGTAGAG | 57626 |
rs530331392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835903 | AGTTTCAGAAATAGA[C/T]AACCTCAAAATTACA | 57626 |
rs530341553 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70060509 | GCCAAAATTTGGAAG[A/G]AAAACCTATTTGTTA | 57626 |
rs530342243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874553 | AGATGTTTCACAATA[C/T]TTCTTTTACTTACAA | 57626 |
rs530348687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013671 | AATTCAGTGTCATAT[C/T]TGCATTTTAAATACT | 57626 |
rs530348786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007147 | CAATATGAGAACTTA[C/T]CAACAAACCGTGATA | 57626 |
rs530349303 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69857417 | TTTCTGTCTCTGTCT[C/T]CCCCTAGTGGACATA | 57626 |
rs530350115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748626 | ATGACATCAGAGAAC[A/G]ATATTTAAATGTTTT | 57626 |
rs530350564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716067 | TACCAAATTTTATGA[C/T]ATTCTGGGTCATAAA | 57626 |
rs530351539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756178 | GTTGTTAATAGTCTT[G/T]GTCACACCCTTACTC | 57626 |
rs530358580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970169 | CATTCTTGAGCATTG[A/C]CTTAATTACTATTTT | 57626 |
rs530360760 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69813087 | CCCAAATGTTCATCA[A/G]TGATAGACTGGATTA | 57626 |
rs530368087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081840 | GTTGTTTTGAACTTA[C/T]GGGTTTGTGGTAATT | 57626 |
rs530372513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70049278 | AAACCAAACCTAATT[A/C]TTTTATTTCTTGTTG | 57626 |
rs530386534 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774690 | CACACACACAAGCAA[A/G]TAGAAATAGCCTATA | 57626 |
rs530403341 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70050397 | AAATATTAAAATTAA[A/G]TTTGAATTTCTGATA | 57626 |
rs530416856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835296 | CCCACCTGGGCAAAT[C/T]ACAAAAAAAATTATT | 57626 |
rs530419634 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69978729 | CGAACTCAGGTGATC[C/T]GCCCGCCTTGGCCCC | 57626 |
rs530419803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878890 | GATTAAGAAAATATG[A/G]TACATACACACCATG | 57626 |
rs530433200 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69887074 | TTGATTAGGTAAGTA[C/T]GAAAAATATAATCTT | 57626 |
rs530438412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928388 | TATCTTCTCATATGT[C/T]AGCCGTATGAATAAA | 57626 |
rs530439050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752886 | TGAATACAGCCTCTC[C/T]GCATCCACTGCTGCC | 57626 |
rs530446374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046365 | AACTTTACAAGTGAA[A/G]AACATGTCACTCAGA | 57626 |
rs530446856 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709774 | AGAGAGGGCAGAAAA[A/C]TGGATGAAACAATAA | 57626 |
rs530449459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054178 | ACATAGATTGTCTCA[C/T]TTTCATTTAGTGATA | 57626 |
rs530451041 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70066913 | GCCTATCTAGACATA[C/T]TCGCTTATTCATAGA | 57626 |
rs530460644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794581 | AAAAAAAAGAGCTGG[G/T]GGAAGGAGAGAGAAG | 57626 |
rs530465400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069901 | AGGCCGGGCACGGTG[G/T]CTCATGCCTGTAATG | 57626 |
rs530482462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053806 | TCCAAGCTAGTTTTG[A/G]CGGGCACAAGAAAGT | 57626 |
rs530488314 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69969412 | ATTTATTACATACCA[A/G]TTAGATAAATTAGTG | 57626 |
rs530491335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867811 | GAACAATGAGAACAC[A/G]TGGACACAGGAAGGG | 57626 |
rs530494701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098761 | AGAGCATTTTTTACT[A/T]TCATAGGATATCTTA | 57626 |
rs530504716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040133 | ATTGGTAATCACAGT[A/G]GATGAAGTTATACAT | 57626 |
rs530510535 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69746431 | AATTAATTTAATTAG[A/C]TACACTAAGAATTAT | 57626 |
rs530511231 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707499 | ATCAACACAATATTG[A/G]ATAAAAACAATCATT | 57626 |
rs530511412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714439 | CAGGAAATCTGAATG[C/T]CAGTTTAAACAAACT | 57626 |
rs530516688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846220 | TCCACAGGCAATATG[A/T]TCTTTCGTTAACAAC | 57626 |
rs530529523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724975 | CCAAGCCTCACCAGC[A/G]TGATTTGGAGCAACT | 57626 |
rs530549028 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69826335 | CATGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 57626 |
rs530551943 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845731 | ATACTAACATGAATA[C/T]TTCTATGAAGGTAAT | 57626 |
rs530559181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885647 | CAAACTCCTTATTGT[C/T]TATGAAGATCATATA | 57626 |
rs530566734 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70015687 | GGGTGATGTAATTGT[C/T]CTGAGCACCTTTAAG | 57626 |
rs530574924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714000 | TCTTATGCTGATGAT[A/G]TGCTTAATGTCTATT | 57626 |
rs530584021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029282 | GGCAGATGAAAGAAA[C/T]TTGAACAGTGACTTT | 57626 |
rs530593586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739539 | TACACAGACAAAATA[A/G]AAGGATGGAGGAAAA | 57626 |
rs530606911 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985770 | GGATAAACAAAAATG[C/T]GATCCATATATATAT | 57626 |
rs530607018 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778923 | CCTGCCTCAGCCTCC[C/G]GAGTAGTTGGGACTA | 57626 |
rs530623048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703519 | ATTTTAAAATAAGTT[G/T]AGTGTAGCCTAAGTG | 57626 |
rs530626125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932394 | CTGGAAGACCCTGAC[A/G]TTTCTTCCTTCTGAC | 57626 |
rs530631519 | snp | A/G | 2.58301e-05 | 0.00359366 | utr-variant-5-prime, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107723 | CACAGAAGGCAAAAG[A/G]CTGGCAGCTCACGCA | 57626 |
rs530643964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747057 | ATGCATGGAGAAAGT[C/T]GAAACAAATGTTGAG | 57626 |
rs530644820 | snp | C/T | 4.95315e-05 | 0.00497627 | missense | KLHL1 | GRCh38.p7 | 13:69719493 | TCTTACACATGGGAG[C/T]ACACATGTTCCACTT | 57626 |
rs530659313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892986 | CTGGGATGAATAATT[A/T]ACTAGTTGCTTACAA | 57626 |
rs530659477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073603 | CATCACAGTGAGACC[C/T]TGTCTCTACAAAAAA | 57626 |
rs530660736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080658 | CTGGGGTGCAGTGTC[A/G]TGATCTTGGCTCACG | 57626 |
rs530669375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789508 | TTTTTTCATCACTTT[C/T]TGTACAATTAAAATG | 57626 |
rs530670717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783606 | ATGAATAAAATGAAG[C/T]CAGAAGGGAAGTTTA | 57626 |
rs530677238 | in-del | -/AT | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981791 | CAAAAAGTGCCCAAA[-/AT]AAAAAAAAATCTAAA | 57626 |
rs530684933 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872606 | TATCACCCCATAAAA[A/C]CCTCCCGTCACTTTC | 57626 |
rs530694246 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70079903 | CTTGGAAGTGAAGAG[-/T]TTTTTTAGAACTGAA | 57626 |
rs530695130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833884 | ACACACACACATATG[C/T]CATGGAATACTACTC | 57626 |
rs530696090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080089 | TGGAGCCATACAGCA[C/T]ACTGTTCATTAGACA | 57626 |
rs530714552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906279 | ATTACCTAAAACTCA[C/T]CAGAAAAATAATGGT | 57626 |
rs530723355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879799 | TCAGATCCAATTGGA[A/G]TAAAATCTGGTCTTT | 57626 |
rs530731261 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086364 | TAGGTGCTTGGATCA[A/C/T]CTGAAGTCAAGAGTT | 57626 |
rs530740376 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69801562 | ATTATTTTATAAAAG[A/G]TATACTATAATTTAA | 57626 |
rs530752446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69955773 | TCCATTTTTGGCTGT[A/G]ATTGAAATCCTAATG | 57626 |
rs530754377 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70057071 | GCCATGTGAGAAAGA[C/G]TCAAATAAATAAAAT | 57626 |
rs530758298 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69918789 | TTACCACAATGGCCT[A/C]CAACAATTATTCCAG | 57626 |
rs530767458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821341 | TTTTTTTGAGATAGA[A/G]TCTCACTCTGTCGCC | 57626 |
rs530769175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69739260 | GAAGGAAGCACTAAA[C/T]ATGAAAAGGACGAAT | 57626 |
rs530779176 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914201 | TTAATAAACTCCCCT[A/T]TATATATACATCTAT | 57626 |
rs530784827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721493 | ATTTTGGGTTCGCAG[A/G]TGAAATTTTTTCTTT | 57626 |
rs530785311 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70083826 | TACATTGTATACATA[C/T]ATTTAAACACCACAT | 57626 |
rs530785922 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69797664 | TCTACTAAAAATACA[-/AA]AAAAAAAAAAAAAAT | 57626 |
rs530785970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920559 | TATATTGAGGAGCAA[C/T]ATAACAATGTATAAA | 57626 |
rs530789681 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69809729 | ACAGTCTAAACACTC[A/G]ATTTAAAAGACATAG | 57626 |
rs530809133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894509 | AAAATTTGAGTCATA[A/T]CTTTTTTTCCTAATG | 57626 |
rs530811860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774252 | AATAGAGTTCAAGAT[C/G]AAATTGTTTCAAAAG | 57626 |
rs530813529 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105752 | TAACTTTTAATAACA[G/T]TTTATAACTTCATAG | 57626 |
rs530813655 | in-del | -/AATT | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827191 | AATTTTGGTATATAA[-/AATT]AATTTATAAAACATG | 57626 |
rs530814704 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69916596 | GGCCTGTTGTGGAGT[C/G]GGGGGAAGGGGGAGG | 57626 |
rs530821141 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899759 | TGGGATAACCAAATG[A/G/T]CAATACTGGAGTGAT | 57626 |
rs530828176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878806 | CACATGCACACATAT[A/G]TTTATTGTGGCACTA | 57626 |
rs530837353 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005152 | AAATATCTCAATTTA[A/T]ATTATGTGGTTACCA | 57626 |
rs530838662 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815750 | TGGAATATTAAAAAG[A/T]AGGTGATTAACTTTT | 57626 |
rs530839859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903998 | GTTTACTATATGCCC[C/T]ATGTATTTAAAGAGA | 57626 |
rs530845348 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722972 | TCCATTTGTTGGAAC[A/C]CAATGGAATACTATT | 57626 |
rs530845407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100131 | TAGATCAACTGGAGA[A/T]GAATTAACCACATTA | 57626 |
rs530846862 | in-del | -/A/AA | 0.00914312 | 0.0669923 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877036 | AGCATAACTCTGTCC[-/A/AA]AAAAAAAAAAAGATA | 57626 |
rs530847855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789177 | GAATTTAATTTATTC[A/C]ACAGGAATCTTTAGG | 57626 |
rs530848758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927247 | CACCTTTACTTCACA[C/T]CATATAAAAATTAAC | 57626 |
rs530850613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920164 | GGCTCTTTCTATTCA[C/T]TTGAAAGAGTTTTTT | 57626 |
rs530851761 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69865886 | TCTTTATATTTCAGG[C/T]GTAATTTATTTATCT | 57626 |
rs530854001 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70029805 | TTAAAAGACACAGAC[C/T]GGCAAATTGGATAGT | 57626 |
rs530864512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961950 | TAGTAACATATTATT[C/T]TTTCATAAGTAGAGT | 57626 |
rs530879023 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69890171 | TTAGTGATTTGAAGA[C/G]GGTGACAATGGAAGT | 57626 |
rs530882922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040649 | ATTTTCTATTTGTCT[C/T]TAGTATTTGTAAGTT | 57626 |
rs530893103 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69704779 | TCCCTCCAGGGGTTG[C/T]ACCTTTCAGCATGAG | 57626 |
rs530912485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066862 | AGAATGAAAAATAGT[C/T]ATTTTATATAACAGC | 57626 |
rs530913194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727275 | TCCTGTTAATACTGA[C/T]CTTGCCACACAGATC | 57626 |
rs530917537 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69974550 | ATAAAAGACTACAAG[A/T]TTGAAGAAATTATAG | 57626 |
rs530923976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061807 | CTTTTTTACCTTTTA[C/T]ATTTAGTTGACACAT | 57626 |
rs530937679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779344 | CTTCCTTCCTTCCTT[C/G]CCTCCTCTTTTTTCC | 57626 |
rs530945525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980921 | TTTGGTCAGATACTA[A/G]TTTCAGTTTGTTATG | 57626 |
rs530974814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726427 | ATCTGCCTTTCCATG[C/G]GAAATATTTTAACGT | 57626 |
rs530976417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828795 | AGCTTTCCACCACTT[C/T]CCTGGCAACCTGTAT | 57626 |
rs530987763 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69857450 | ACTTATTATTATATG[C/T]CCCATGACTAGCAAA | 57626 |
rs531000621 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709710 | ATGTTTTGGGTTGAA[A/C]ACATGTTCAGAAATT | 57626 |
rs531001042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067576 | GAGTGGAATTCCTTT[A/G]GCCAGGAAGGATAAA | 57626 |
rs531005333 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69826522 | GAGGCAGAGGTTGCA[A/G]TTAGCCAAGATCCTG | 57626 |
rs531006353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881379 | ATTTTTAGTAACATA[A/T]GGATTAGTAAAAATG | 57626 |
rs531016069 | in-del | -/A | 0.324642 | 0.238597 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958740 | CAAACCTTAAAATTA[-/A]AAAAAAAAAATACAT | 57626 |
rs531020535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841379 | GGACATGAAATCAAT[A/G]TACAAAAGTCAGCAG | 57626 |
rs531023429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023903 | TCTTAGTTATAGTAA[A/G]TTTAGTAACTTACTA | 57626 |
rs531030602 | in-del | -/GG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69913298 | GCTTCCCAGGAGGCA[-/GG]GAGCTATATCCAAAG | 57626 |
rs531037682 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69848221 | AAAGACATACAGAGA[A/G]AAAAATGGACAATTA | 57626 |
rs531039692 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074138 | GGCACCTTAAGCCTC[C/T]GCACCCGGCCCATAA | 57626 |
rs531043055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888063 | TAGAGACTGGAAAGT[C/T]CAACATCAAGGCACC | 57626 |
rs531047418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921479 | AATTATTTCTGAAGT[A/G]ATTTATAGTGCTCCA | 57626 |
rs531048883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928330 | AAAAACTTAAACATC[C/T]GATTCCCTAACTTTT | 57626 |
rs531049404 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006941 | TTTCATTTTGTTTTT[A/T]TATCAAAATACATTA | 57626 |
rs531049908 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815351 | AATGTGGTACATATA[C/T]ACCATGGACTACTAT | 57626 |
rs531079230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755425 | TTATAGATTACCCAG[G/T]CTCTGGTATTTCTTT | 57626 |
rs531080084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100523 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTAAGT | 57626 |
rs531081971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094235 | CTCGGCTGAGGTGGG[C/T]GGATAACTTGAGCTC | 57626 |
rs531083021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859496 | ACGCTGTGACAGCTC[C/T]GGTCCTTCCCTCTAG | 57626 |
rs531086193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013094 | ACATTTAAAAATATC[A/G]GGGAATGATGGCCAA | 57626 |
rs531087726 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006439 | TCTTTCTTGTATTGT[A/C]TTTGCCTGGCTTTGA | 57626 |
rs531117378 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69763046 | TGGATGGGCATCCTT[C/T]GTTAGGTTTCTTTTT | 57626 |
rs531119000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963824 | AAGCTGGTATCAATA[C/T]TGGAAGAAATATCTT | 57626 |
rs531121481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042057 | CTAGTCTTGGTCTAG[A/T]AAAAGCAGGCTTATC | 57626 |
rs531126589 | snp | C/T | 1.64961e-05 | 0.00287189 | missense | KLHL1 | GRCh38.p7 | 13:69719450 | TAAAGAAAACCGTCA[C/T]ATGTGGCCACTCCGA | 57626 |
rs531142565 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754779 | CCATTGTTCGAGTCT[C/T]ATTTTTGTTACATTT | 57626 |
rs531153178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767637 | ATTTTAATAGATTGA[C/T]CACCCATATGATGAT | 57626 |
rs531164385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946650 | CCCACGTAGGTGAGA[C/T]TACAGGCATGCACCA | 57626 |
rs531166263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880718 | GAGTTGGAAACGAGG[A/G]CATAAAAGAATGACA | 57626 |
rs531173568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030970 | ACTATAAACACTTCT[A/G]TGCAAATAAACTAGA | 57626 |
rs531179942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734880 | ATACACTTCTCATGA[C/T]TAAAGTCAATTATAG | 57626 |
rs531181387 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087933 | GGTTGGGGGCATAGG[G/T]AAGGGAGAGCATCAT | 57626 |
rs531190409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908904 | TAGGCTACATTATTT[C/T]CCATATATATTTTAA | 57626 |
rs531195241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968752 | TAAAGAAATGCTCAT[C/T]ATTTTTTATGGCTGC | 57626 |
rs531202945 | in-del | -/A | 0.487909 | 0.0768079 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031116 | ATAGCCTGCCAACCA[-/A]AAAAAAAACCCAGAT | 57626 |
rs531206129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760979 | ACAGAATCTCCCATT[A/G]TTGCCAGAGAGCAAT | 57626 |
rs531211053 | in-del | -/AA | 0.424503 | 0.179021 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940793 | TTTTATCTTAAAGGC[-/AA]AAAAAAAAAAAAAAA | 57626 |
rs531228444 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69932349 | TTGATTTTATTTGTG[A/G]AAGACTGTGCTTTAT | 57626 |
rs531232222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840703 | ATATATATATATATG[C/T]ATGTATGTATGTATG | 57626 |
rs531242874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741519 | TTACTCATAGCAACA[G/T]CAATAATCAGAGTAC | 57626 |
rs531251300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915953 | TGAACAGACACTTCT[C/T]GAAGACATTTATGCA | 57626 |
rs531256641 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714996 | GCAGATAAATTATCA[A/T]GATGCCAGAAAAATT | 57626 |
rs531260860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785827 | TGATAAAGGGGATAT[C/T]GCCACCGATCCCACA | 57626 |
rs531275168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000388 | TAGAAGTATAAAAAC[A/G]TTAAGAAAAATCCAC | 57626 |
rs531284964 | in-del | -/A | 0.198827 | 0.244707 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703450 | AGAGTTTAAAAAGTA[-/A]AAAAAAAAAATTACA | 57626 |
rs531289338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088640 | GTCAGCTACAATCAC[A/G]CCACTGCACTCCAGC | 57626 |
rs531295792 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70103198 | AAAGGATAGTCTCTA[C/T]GCAAAGAAGGAAAAC | 57626 |
rs531316848 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900487 | TAGCGTTTTTCACCA[A/C/T]TGTTCCCAGTAATCC | 57626 |
rs531318923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988131 | ATCCTACACCCTCAA[A/G]TTGGCCCCAGTGTCT | 57626 |
rs531333007 | in-del | -/TTTTCT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69801856 | AATGCCCATTGATTA[-/TTTTCT]TTTTATTATTTTTTA | 57626 |
rs531334241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710164 | ATAATAAACTAATTT[A/C]CAAAGGTTTAAGTTC | 57626 |
rs531334373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703066 | GATGATTTTCATGGA[C/T]TGTCTCACATCAGAG | 57626 |
rs531342499 | in-del | -/GAGAG | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736676 | GGATAAAGAGATTGT[-/GAGAG]GAGATATATATATGT | 57626 |
rs531354398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036129 | TATACTTTTATTTTA[C/T]TTGAGAATAAATGAC | 57626 |
rs531355135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042723 | TGAGCACGGACTCCT[A/G]TGTTTATTTAAAAAT | 57626 |
rs531357154 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69798472 | ATATTGCTAAAATTA[C/T]AGGTTCATTCCAATA | 57626 |
rs531370388 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027188 | TTTGTGGCTGTTTTT[-/A]AAAGTATAACATTTT | 57626 |
rs531373578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942164 | TGAATTGTTTCATTT[A/G]TATTTTCATTTATAT | 57626 |
rs531375966 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075477 | AAACTTATTTGCTCA[A/G]AAACAACTGAAGCAA | 57626 |
rs531393793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057325 | AATCTTAGAACCTTA[C/T]AGCTTCACTGCTGAT | 57626 |
rs531394754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915480 | CAAACCTGACAAAAA[C/T]GAGAAATGGGGAAAC | 57626 |
rs531396449 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783274 | GCAGAGCACCTCTCC[-/T]CCTCCAAAGGAATGC | 57626 |
rs531403685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977686 | TATAGAAACACCTAA[A/T]ACACTGATTTGGAAA | 57626 |
rs531407684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769427 | GTGACAGGAGACAGA[A/C]AAATTCCTAGGCAGA | 57626 |
rs531413013 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074972 | TTTAAAATACCATTT[A/T]TAATAATGGAGGTGC | 57626 |
rs531420252 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69768468 | GACTAATCAGGGAAA[C/T]TTAAGCCTAGAATAC | 57626 |
rs531425198 | in-del | -/TC | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966605 | ATATTTCATTTCTTT[-/TC]TTTTTTCCTTTTTAT | 57626 |
rs531428921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056552 | GCTCATAAAACATTA[C/T]CAAAGATAGACCATA | 57626 |
rs531433587 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811001 | ATCAAATAAAAAAAG[C/G]CCTATACCAGATGGA | 57626 |
rs531435658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063183 | GCTCTGATTACTTCT[C/T]TAAGTAGACTATGCT | 57626 |
rs531438831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999991 | TTTGGGTCATGGGGA[C/T]ACATTCCTCATGAAC | 57626 |
rs531443504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874420 | CCTGAATGATGCATT[C/T]GACTATCTACTCAAT | 57626 |
rs531449070 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785265 | TGGAAGTAAAGCACT[C/T]CTCATCAAATGTAAA | 57626 |
rs531463549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957424 | TATCAGGATTTGACT[C/T]TCAATTTTTGGTCAT | 57626 |
rs531468548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855018 | ATAAATATATGTATA[A/G]GAATATATGTATTAC | 57626 |
rs531472583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069533 | CAGATATGGCAGAGA[A/G]TTCAGAATTATAAGA | 57626 |
rs531474924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901406 | TTAATTTCCAAGAAT[A/G]AGTTGAGGGATAAAT | 57626 |
rs531485712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013873 | TATAAAGCACTTTCT[C/T]GCTACTTGTTATAGA | 57626 |
rs531490293 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715543 | TTTTTTTTTTTGAGA[C/T]GGAATCTCGCTCTGT | 57626 |
rs531497129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025747 | CATGTTTTAAAAATA[G/T]GTACAGGCATATATA | 57626 |
rs531499693 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69967713 | AAGATGGCAAAACCC[C/T]GTCTCTACTAAAAAT | 57626 |
rs531508220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007516 | CATACATAGGATAAA[C/T]ATCTAGGTAAAAGCA | 57626 |
rs531511608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735435 | CCTTACTAGTTTATT[A/G]AATGTTTATCTTTCT | 57626 |
rs531511978 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70062622 | AATAAAAAGTGGATA[A/C]TCAGTAAGTTGTGTC | 57626 |
rs531525651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803790 | TGCAAGTGGTCTCTA[A/G]AAGCTGAGAATGATT | 57626 |
rs531526068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817557 | TCTCTAAATCTTTTA[C/T]TTATTCTCTGCAAGT | 57626 |
rs531542550 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895780 | GGTGTGGTCTCGGCT[C/T]ACTGCAGCTACCATC | 57626 |
rs531543518 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977025 | GAAACCTAGAGTTGT[A/G]TCAGTGAAAATCTCT | 57626 |
rs531547120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982415 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 57626 |
rs531553770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750114 | TTTAATCATTGTATT[A/G]AATTACTAAATTATT | 57626 |
rs531555402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861774 | CCAACATGGAGAAAC[C/T]CCGTCTCTACTAAAA | 57626 |
rs531556198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958376 | TGGATGAGTTCAACA[C/T]GGAGAGTGTTTCCCA | 57626 |
rs531558081 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965908 | GGCTGAGAGAGGTGA[C/T]GAAACTGCAGAAGAA | 57626 |
rs531563365 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69900344 | CCAGCTTTGAATATA[C/T]CTCAATGCATGCTGC | 57626 |
rs531571419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831075 | CAAACCCAAACCCAG[C/T]AGAAGAAAAAAAAAA | 57626 |
rs531596239 | in-del | -/ATTAA | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864286 | TCATCTAAAAAATAC[-/ATTAA]ATTAAAATATTATAA | 57626 |
rs531597489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107146 | CCACATGAGCACACG[C/T]GGTGAAATGAGTGGA | 57626 |
rs531600342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876040 | TTTGGCCTTACTCAT[C/T]TGTAAGAAAATAAGA | 57626 |
rs531601036 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69962985 | AGTTATTTCTTCATA[C/T]ATTCACTTTTGCATC | 57626 |
rs531609860 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981981 | AATATGTGAATAGTG[A/T]CATAAAAAGTTTTAA | 57626 |
rs531610839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836975 | ACTAAGAAGGGAAAT[A/G]TAAATGTAATGATGA | 57626 |
rs531612374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749589 | TATCGTTAATTTTCA[C/T]GTAACATGGCACATG | 57626 |
rs531622445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019626 | AGTTGCTATTACTAC[C/T]TCTATTTTACAAATG | 57626 |
rs531639046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068944 | GAAAAAGCCTTCTTG[C/T]TTCTGGCAGAGAAAG | 57626 |
rs531639585 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084324 | CATGAACAGATCATT[A/T]AACCTTTCCATCTTA | 57626 |
rs531646777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050269 | TTACATATTTCTGAC[G/T]CCTTCTTCCTTCTTA | 57626 |
rs531647959 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058892 | GACAGAATAGAGAAC[A/C/G]CAGAAACAAATCCAT | 57626 |
rs531656076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090600 | ATAATCCTTTTCTCA[C/T]GATGATATAGGGAGA | 57626 |
rs531664680 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69822650 | TACAAAAATATTACA[A/T]GTTATGTGCAACAAA | 57626 |
rs531665700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775011 | GGAACAAACTTTAAT[C/G]TGTATTAAATCTGAC | 57626 |
rs531705824 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037424 | GCAATTCTGGCCTGA[A/G]CATTTGGTTGAATCA | 57626 |
rs531714090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076166 | AACTGCAAAATACAC[A/C]GAAGATTCAATGCAA | 57626 |
rs531721895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935911 | GAACAAAAAAATTCA[A/G]TGGAGAATGCTTCTT | 57626 |
rs531722227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096427 | TATAGCTTTGATTTA[C/T]ATTTCTCTGATGATT | 57626 |
rs531726519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849349 | AATTCTACAATATAA[C/G]TCTTTTTAATCTATA | 57626 |
rs531731733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704331 | TCAGCAAGCCCTCTA[A/C]ATATCTCTCCAACAA | 57626 |
rs531733934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711566 | CATTATCAAAAGAAA[A/T]GTTCCTAGACTTTAA | 57626 |
rs531745381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043617 | ATCATTTTTACTGTA[C/T]CTTTTCTATGCTTAG | 57626 |
rs531774018 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863466 | GTGTTGAATGAATTC[C/T]GAATAGAGTGTATAT | 57626 |
rs531774053 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983608 | AAGAAGAAGAAGAGA[A/G]AAAAAAAAAAAAGCT | 57626 |
rs531782753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008911 | GATCAATATTATTAT[A/C]ATTCTTGTCACAATA | 57626 |
rs531786586 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69816915 | GTGGGCCAAGATGGC[A/G]CCACTGCACTCCAGC | 57626 |
rs531788743 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70023395 | TCACCTAAAAATATT[C/T]TGGTATCAGTTCCTT | 57626 |
rs531794314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791527 | CACACTACATGATTT[A/T]AAAAACTACTACAAA | 57626 |
rs531798371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776384 | GCAGAGAATTCTAGA[A/G]CAAGCTTTGCCACTA | 57626 |
rs531805212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095831 | CCCTTCTCCCTCCAC[C/G]CCCCCCACCACACTC | 57626 |
rs531811495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763539 | GACTGAGATGACAAA[A/G]ACTCAAATAAATGTG | 57626 |
rs531820776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008479 | TATGTGGTACACTCA[C/T]GTGCGTCATTGGCTA | 57626 |
rs531822097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836245 | AAATTGCAGCTCAGG[G/T]CAATCAAGGCAGTCA | 57626 |
rs531828378 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952799 | AAATGGACTCTTCAT[A/T]AAAAATGGCTAAGTG | 57626 |
rs531828585 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077785 | AATTGATAATGAGCT[G/T]AACATTTTAGAAACA | 57626 |
rs531835495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804609 | GCCATTTTACAAACT[C/G]ACAAAGTAGAATGAT | 57626 |
rs531839947 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929166 | AGGACCATTTTGGCG[A/G/T]TCTTAAACAAACTTC | 57626 |
rs531842328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70089936 | TACATTAAAGTAACC[A/G]AAGCTAGTTATGATA | 57626 |
rs531843582 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798439 | AGCAATAATTAGATA[A/C/T]GTCAAATCTGCTTTC | 57626 |
rs531850394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881971 | TTACATATATATTAT[C/T]TAATGGATCTTCACA | 57626 |
rs531855902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014662 | TTATTCCAATTGCTG[C/T]AGGATCTTTATGTAA | 57626 |
rs531856309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870373 | ACATTCATGAGGGAT[A/C]TACCCCACGACCCAA | 57626 |
rs531861219 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708325 | TTTTTTGTTTTAATG[C/T]ATGGTCCGCTTTGAG | 57626 |
rs531866934 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947905 | TGGAAAGAAAAGTAA[C/T]TCTACATTTTCATTC | 57626 |
rs531898890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083484 | TTTATTTCTGAAGGA[A/G]AATGAGATACTTATT | 57626 |
rs531903388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743203 | TAAATTTGAAGTTTG[C/T]TATAAGAGCAATGGA | 57626 |
rs531910747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959141 | TTTTTGTATCCTGTC[C/T]GCCCTCTACAAGCAG | 57626 |
rs531912927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729662 | TAGGAAAAGTACCCA[C/G]ACATTAATAGCCAGT | 57626 |
rs531932465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951001 | ACTCAAATGAAATAT[A/T]TGTCTCAGATTTTAA | 57626 |
rs531942272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032349 | GAAAATCTGAAGCCA[A/G]TGTGCTTAAATATCA | 57626 |
rs531949680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972868 | TCCAATTTTAATATT[A/G]ATCTGTCAACCTAAT | 57626 |
rs531952852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829156 | AGCATTAGAGGAAAC[C/G]AGCACACTAAACACA | 57626 |
rs531953506 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714552 | AAAACCATAATTAGC[-/A]CTATAAATCCAAATT | 57626 |
rs531961787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038268 | CTGCTGAGCATTATT[C/T]TGTGGTAGCAATGTA | 57626 |
rs531963921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957353 | CAAATTTGTTTAAAG[A/G]CTTATGACATTTTAA | 57626 |
rs531985104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825043 | ATGATAGATGGATAC[A/G]TATGTGATAAAGCCA | 57626 |
rs531985882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035367 | TTCTCAATTGTTTGT[A/G]GGAGCTAAAAATAAA | 57626 |
rs531987921 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70042003 | AAAGTAGATTGTTTA[A/T]CATCTAAAAGTTTTC | 57626 |
rs531989801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828712 | AACTCCAGGCTGATG[C/G]TGGGACAAGGTGGGA | 57626 |
rs531992455 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70010032 | CATTACAAGAAGGAG[-/A]AAAAAAAAAGCAAGG | 57626 |
rs531994971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956876 | GTTTCTGCTTTGCAC[A/G]TGCTTAGCATAGAAA | 57626 |
rs531997410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69862742 | GGAAGAGGAAGAGAG[A/C]GATCTCTCTCTGTTT | 57626 |
rs531998461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69874238 | CCCCTTTAAATGCCA[G/T]TGCTTCTAGTCTCCA | 57626 |
rs532007429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787176 | TTAAAGTTCATATGG[A/G]ACCAAAAAAGAGCCC | 57626 |
rs532032653 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69935875 | TGATGAATGTATTAC[A/G]AGATACTAGACACTT | 57626 |
rs532037141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876525 | GTCCTTGTTATTTTA[C/T]TGTGCTTGTTATTAG | 57626 |
rs532048097 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922080 | ACTAAACGTGCACAC[A/G]ACAGTGCCTGGCTAA | 57626 |
rs532056404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074302 | CTACAGTTGCCACTC[A/C]TTTCTGTCGTCTGTC | 57626 |
rs532057452 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038463 | GAGTATATTTACTAA[C/T]TTTTTAAGAAACTGC | 57626 |
rs532063368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924152 | GGAGCTTGGTGCTGG[C/T]TTGCAGGTGCTCCTC | 57626 |
rs532067319 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036539 | ATGGGTGTATATATG[-/A]AAATGTTTTATTCAG | 57626 |
rs532067655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916909 | TTTTAGAAGCCATAT[A/G]CACAATATAGTGCAA | 57626 |
rs532075512 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709605 | CCTTTTAATAAGCAA[A/T]TATTGAAGTTTTTAT | 57626 |
rs532091613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080874 | CCAAAGTGCTGGGAC[A/G]TGAGCCACCACGCCT | 57626 |
rs532137393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69840626 | TGGCTCAGTTTCCTT[C/T]TGTTGTATACTAATA | 57626 |
rs532138933 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785188 | TGAGCCACCGCGCCC[A/G]GCCCAGAATATACAT | 57626 |
rs532139260 | in-del | -/AACA | 0.00361662 | 0.0423702 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790551 | CTTCCACAAAATACT[-/AACA]AACAAATAAAGAAAT | 57626 |
rs532152262 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976231 | TCATAGTAAATGTTG[C/T]CTTGCAGAAATAGGT | 57626 |
rs532153850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048174 | CTCAAATATACTTTC[A/C]CTAGATTTTCAAAAA | 57626 |
rs532162109 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69921885 | CTAAGGGATAAGGGA[A/G]TACTTAGGGAGTTAT | 57626 |
rs532173194 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70000998 | AGTAATTGGCAAAAT[A/G]TAGAAAATATGGATA | 57626 |
rs532174869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062485 | TTCTGCCATTCTATT[G/T]AAATAAAACTTCAAA | 57626 |
rs532175372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915022 | TTTCAAAATCTCTCA[A/G]GAAGCAGGGACTTAT | 57626 |
rs532183628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921427 | ATGTTGTCAGATATG[A/G]AAGGAGAGTTGCTTA | 57626 |
rs532184486 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728219 | GAAGAAGAATACCAA[A/C]ATTTGAATAAAAAAT | 57626 |
rs532192327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69993257 | TCTGGGAGAGCCATA[A/G]CAGAACCACCACGCT | 57626 |
rs532195431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854499 | CACATTGGTTACCAT[A/G]AAGTTTGGAGAGGCC | 57626 |
rs532206779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061927 | ATCAACTCAAACATT[C/T]TTCACTTCTTCATGT | 57626 |
rs532209292 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761946 | CTTTAGTTTGTCAAA[-/C]CCATAATTGTTGAAA | 57626 |
rs532210558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068855 | GGGGCTCAGTCTCGT[C/T]GTGGGGGAGGAGGCA | 57626 |
rs532211848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774948 | TTTTTCATTTTTAAT[A/G]TTTCTTGAACAGAGG | 57626 |
rs532224052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087289 | AAAATATAGTAAATT[G/T]GAGGGTAAAATAACA | 57626 |
rs532235650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69980497 | AGTTTCAGCTACACC[A/G]AATAATTTCAGTTTC | 57626 |
rs532248496 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962499 | TCTGTCACAGAGGCA[-/T]TTTGTGTTTTTTTCT | 57626 |
rs532250920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816622 | TAAATATTTCTTAGC[A/G]CTATAATTAAAGTTG | 57626 |
rs532252751 | in-del | -/AGAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69749320 | AAATAATTATCTAAT[-/AGAA]AGAAAAGAAACATCT | 57626 |
rs532256611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880615 | GTATAGCCTTAGGAA[C/T]AAAAAAGCCAACAGG | 57626 |
rs532260355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963063 | TTTGTTTGTTTATAA[C/T]TTCAGCATTTTTTTT | 57626 |
rs532273104 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780755 | ATATACATATATATA[C/T]ATACACACACATTTA | 57626 |
rs532277775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734344 | CTTCCTACATAGCCT[G/T]AAGAAGTGACAGCCA | 57626 |
rs532278570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075401 | ATCTTTGCTCACAGA[C/T]AACATAATTTTCTGT | 57626 |
rs532288108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019317 | TAATAGGAAGAAAAA[C/G]ATACTGAATGCGGGA | 57626 |
rs532292327 | in-del | -/T | 0.465368 | 0.126951 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006502 | GTATTCCCCCTCAAG[-/T]TTTTTTTTTTTTTTT | 57626 |
rs532300248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018963 | TAATGGAGATATCTG[C/T]TAATCAAGTGCTATA | 57626 |
rs532309487 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69854984 | TATGAATATTTAATG[A/T]AAACACTTATTTGTA | 57626 |
rs532317981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860250 | CACAAGATATGAAAA[A/C]TCTCAATGTTCAAAA | 57626 |
rs532319041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69986953 | CTTTGTATTAGATAT[C/T]CAACAGTAAATAATA | 57626 |
rs532323674 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835298 | ACCTGGGCAAATTAC[-/A]AAAAAAAATTATTTG | 57626 |
rs532335801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901135 | TAGAATAGAATGGAA[A/G]CAACATTTACAGAGC | 57626 |
rs532342609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106646 | GTAAAAGGACCAGAA[A/G]AGAAGTTGGGACAGA | 57626 |
rs532350568 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923712 | ATGAATATGGCAGTC[C/T]ATCTAGAGCAGCTGC | 57626 |
rs532351184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900406 | TGAACCAACAGCTGA[C/T]ATTTGGTTATATATC | 57626 |
rs532355479 | in-del | -/AAAC | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014791 | AAACATAGTAGACTT[-/AAAC]AGATAAACAGACGCT | 57626 |
rs532364738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971085 | TAAAGTCATTATTTC[A/C]GTACCCAGATTGCCT | 57626 |
rs532376703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970281 | TAAATTAAACTCAAA[A/G]CTTTCCCACTGATAT | 57626 |
rs532377735 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69776942 | TATCAGGTTAGTTTG[C/T]ACCTTTTGATATAGT | 57626 |
rs532384172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050216 | ATGTCATCAAAAGGA[A/T]ACCTTTTGATCAAAA | 57626 |
rs532398267 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69709904 | AACTTTAAAGTGAAT[A/G]ATTTATGTAGAATAC | 57626 |
rs532398348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798387 | TAATTAAAGTAAAAA[C/T]GATACAATTTATGCT | 57626 |
rs532403998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774485 | ACTTTTGCCATATCC[C/T]CTCTCTCTTCTCAGG | 57626 |
rs532413540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088932 | AAATCTATTTACATA[C/T]GTAGTTTGGCTCTTA | 57626 |
rs532420747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057236 | AGATTGAACCATGAA[A/G]GAATCCAAAACCTCA | 57626 |
rs532436719 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888966 | ATGTCCCTTATGGAG[G/T]ATAGCAAATATCAAG | 57626 |
rs532443795 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012755 | CTCTACTAAAAATAC[-/AA]AAAAATTAGCCAGGC | 57626 |
rs532444263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074872 | TGTGTAGATAAAAAA[A/T]TTTAAATTCTGTAGA | 57626 |
rs532446672 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69849270 | TAGGCTATATTTAAG[A/G]GTATACATTAGTTTG | 57626 |
rs532455000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848881 | AAAATTAACCGAAAT[G/T]AAAGTTCTTATTAGC | 57626 |
rs532467216 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030350 | AGTTGGAAGTAAAGC[A/T]CTCCTCAGCAAATGT | 57626 |
rs532492970 | snp | C/T | 1.69401e-05 | 0.00291029 | missense | KLHL1 | GRCh38.p7 | 13:69940192 | GAAGAAGGCACGCTG[C/T]AGCAAGAAGGTTCTC | 57626 |
rs532496375 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007977 | ATATAAGATTATAAA[A/G]TTTATAATTTTATAT | 57626 |
rs532496489 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69872501 | TCTTCATTACCATAA[C/T]ACACAATCCATGTGC | 57626 |
rs532501107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941321 | ACTATACAAATGCAT[A/G]GAAGTTAATACTCTG | 57626 |
rs532503420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101629 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 57626 |
rs532512334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722399 | ACAACCTACCAAGAC[G/T]AAATCATGAAGAAAT | 57626 |
rs532525308 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054760 | GAAATTCTGGAGCTG[-/A]AAAAATTCAAAAGAA | 57626 |
rs532536063 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69832973 | GAATCAAAGACTTAA[A/G]TCTAAGACGTAAAGT | 57626 |
rs532536401 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69783253 | GAAAACCTGGAAACT[C/T]TAAAAGCAGAGCACC | 57626 |
rs532543781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710492 | CAAAACAAAATCTGA[C/G]TGACCTGACATAGAC | 57626 |
rs532558936 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786826 | TCAGGATACAAAATC[A/C]ATGTACAAAAATCAC | 57626 |
rs532568817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824398 | CTCTGATGTTTTTCA[A/T]GAATATGTTTTTTAC | 57626 |
rs532572806 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70052777 | AGGTTAATTTCAACA[C/T]AATTAGGGGTAGGAA | 57626 |
rs532573903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797810 | CCCCAGCCTGGGTGA[C/T]AGAGCGAGACTCCAT | 57626 |
rs532576815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909941 | CTCTCACAGCGTCAA[G/T]GATCCTTTCCTTTGT | 57626 |
rs532583273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869292 | TCTTCCAATTTATTC[A/G]GAGTATTAAATTAGA | 57626 |
rs532594331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722832 | GGTGTATATTCAAAG[A/G]AAATGAAACCAGTAT | 57626 |
rs532609308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958262 | TAATAATAATAATAA[C/T]GTAAGTCTACATGTT | 57626 |
rs532612015 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69812674 | TGATATGAACAGGCA[C/T]TTCTGAAAAGAAGAC | 57626 |
rs532641902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875898 | TTTGTAGAGAAGACT[A/G]TCTCAATAATGATGG | 57626 |
rs532649891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082672 | TACCTGGGCATATTA[C/T]GTGATGCTGAAGTTT | 57626 |
rs532667816 | in-del | -/AGT | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976357 | ACTATTAAACAAAAA[-/AGT]AGAATGTATTAACTC | 57626 |
rs532668526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013181 | GATAAAGAAGAAATA[C/T]AAACAAGCAAAGAAT | 57626 |
rs532668992 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70079089 | CAGAAATGCAAACTA[C/G]ACAATCATCAACCAA | 57626 |
rs532675726 | snp | A/G | 0.000164981 | 0.00908093 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882268 | ATCTATTTAAACAGC[A/G]TCACACATCATTACC | 57626 |
rs532677609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69875172 | GAGGAGTTTGGTGAT[G/T]TTCATTAGGGCAAAT | 57626 |
rs532679223 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001567 | ACATTGGGATATCTA[A/T]CTATGATCTATGTGT | 57626 |
rs532680441 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69939731 | GCCTGGAGCCTATGC[A/G]CCCCTCTCCTCATAC | 57626 |
rs532686747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019546 | CTTATTACATACTCC[A/G]TGCCAGACGATCTGC | 57626 |
rs532693712 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69732386 | AAAATGAATCTCCAA[A/G]TAGTAATTTAAAAGA | 57626 |
rs532717826 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008401 | TCATATAAGTTTTTG[C/T]CATTCTATGAACATA | 57626 |
rs532720148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965114 | TTTGGTTTATCTGAT[A/G]GAAAATGGAATTACA | 57626 |
rs532722912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038157 | TAAATTTAATATACA[C/G]TAAAGTGACCTTTGA | 57626 |
rs532738246 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70055772 | GGAGTATAATATTTT[A/G]TTTGCAAGTCACATT | 57626 |
rs532760652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830844 | TAATCTGATCCTGAA[C/T]GATTGTTGGGTCAAC | 57626 |
rs532760986 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037402 | TTGAGAACTCAATAT[C/T]AGTATTGCAATTCTG | 57626 |
rs532762265 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108079 | GAGCGCTCCGAAGCT[A/C]CGGAGGCGGCTGCAG | 57626 |
rs532767067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909936 | AGTTCCTCTCACAGC[A/G]TCAAGGATCCTTTCC | 57626 |
rs532768234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902671 | ACAAAAACCAAACAC[C/T]ACATGTTCTCACTCA | 57626 |
rs532769409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723750 | GGAGATTTCATCTAC[A/G]TGATAAAACCTAGGT | 57626 |
rs532769429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978243 | TACTATTGACTCTCA[C/G]GTAGAAAGGATAATT | 57626 |
rs532778485 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715954 | TTACCTCTTGAGGCC[A/C]TATCTATCTCAAAAG | 57626 |
rs532778586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750009 | TTGTATCTTAATTTG[A/G]AAAGCATTAGCCTGT | 57626 |
rs532784902 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076444 | TATGCAGAAAAAAAA[A/C]ATCAAGACACTGACT | 57626 |
rs532805625 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916290 | AAAGACACATGCACA[C/G]GTATGTTTATTGTGG | 57626 |
rs532827974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983515 | GGAGGTCAAAGCAGG[A/T]AGATTTCTTGAAGCC | 57626 |
rs532840316 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69979141 | GAAAGAATGGGATTA[A/G]AAAAACAGAAAATTA | 57626 |
rs532840772 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69889932 | CTTGCTAGCTCTAGA[A/G]GCTACATTAACATTA | 57626 |
rs532855502 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923017 | AATGAATTATTTAAA[G/T]AATTAGGTGGGAGGA | 57626 |
rs532867456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957856 | CTTATACTGCTAATT[A/T]AGAATTTAGAAAAAT | 57626 |
rs532873262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995495 | TTATTTAAATTAGTT[C/G]AGAAATTCAGAAGCT | 57626 |
rs532875160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989081 | TATCTTCCAGGATTT[C/T]TATAGTTTTATGTTT | 57626 |
rs532882895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710987 | TAGCGGTTAAAATTA[G/T]CTACAAAATGAAAAC | 57626 |
rs532894328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077158 | AAAACATGGATTCAT[G/T]CACATTTTTGCACAA | 57626 |
rs532901591 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036832 | TGATTTTAATGCCAT[A/G]GTCTTTTTTTTTTTT | 57626 |
rs532902009 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892141 | GAACATCGGTATTTG[A/C]CAATATTCTTTAGGT | 57626 |
rs532902828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812625 | CTCAAATTTACAAGA[A/G]AAAAACAAACAACCC | 57626 |
rs532903222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043501 | TTGGCCTTCACATTC[A/G]CTCACTACTTACTCA | 57626 |
rs532914793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032231 | GACGTAAAAAGACTT[C/G]ATGGGAGATACTAGT | 57626 |
rs532921669 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69765784 | ACCCAGGCAATGCTA[C/T]CCTCCGATCTGTTGC | 57626 |
rs532926713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821819 | CACATAAACTATTTT[C/T]GACTAACTTTTTTGC | 57626 |
rs532931148 | in-del | -/AAG | 0.0011988 | 0.0244533 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924719 | CACGTTGTGTACAAC[-/AAG]AAGGAGAGAAGAGCA | 57626 |
rs532934839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751191 | TGTTATGTGTAGGTG[C/T]ATGAAATCAAGGCTG | 57626 |
rs532943000 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69878923 | ATACTATGCAGCCAT[-/A]AAAAATGATGAGTTC | 57626 |
rs532944528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776732 | CCCCAGAAAAACTTA[C/T]AAAAACAAAAGCATG | 57626 |
rs532946277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896261 | CTTATTCTCCCATAT[A/C]TCTGATTGGCACTTC | 57626 |
rs532955048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008923 | TATAATTCTTGTCAC[A/G]ATACAATGCACTTCT | 57626 |
rs532956416 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69702394 | AATAATTTTTACAGA[A/G]TTTGTAATGAAAATT | 57626 |
rs532959144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800017 | GTGGAACAATTTCAC[A/C]CTGAAACCAACCCCC | 57626 |
rs532968702 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044859 | CTGTCAGTTTTTCAA[C/T]AGTCAGCACACCAGG | 57626 |
rs532978786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856655 | GCAATCACCTTACTT[G/T]GTTATTACACTATAC | 57626 |
rs532980185 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70066283 | TAGTCTGTCTAAGTC[A/T]TCTAGCAATGAGAGA | 57626 |
rs532987308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837595 | GTTATACTATATATA[C/T]ACACATACATCTCTC | 57626 |
rs532988523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819033 | GCCATAGGATGATTA[C/T]TATTAATTAAATGCT | 57626 |
rs533003618 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863210 | CTTTTATTTTTGTTT[G/T]TTCTCATATATTCTA | 57626 |
rs533009359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718227 | TCTCGCTTTTCTCCC[A/G]GATACAAGTTGGGAT | 57626 |
rs533013788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883487 | ATTTGACCTGGTCAC[A/G]CCTTCACTATCCCCT | 57626 |
rs533019865 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009662 | TAAATGTGGTCAAGA[A/C]AACCTGTCTCCATGT | 57626 |
rs533033026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942320 | ATTTGAAATTTGAAT[A/G]TAAGACTTTAGGAAA | 57626 |
rs533036598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015829 | CAAGGTATATCTGTA[C/T]AAACTGTATACATGT | 57626 |
rs533045417 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70087288 | AAAAATATAGTAAAT[A/T]TGAGGGTAAAATAAC | 57626 |
rs533055377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069880 | AATGAGAGAAAGAAG[C/T]AGATGAGGCCGGGCA | 57626 |
rs533055695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930387 | AACCATTACAAAGTA[C/T]CAAAAGCTTTTCAAA | 57626 |
rs533060046 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70014318 | ATGATCTCTGCAGGG[-/A]AAAAAAGAGAGTAAA | 57626 |
rs533073756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021417 | CATTCACATACTGAA[A/G]GGCATTTTCATAGCT | 57626 |
rs533084661 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70094070 | ACTTACCAGTAGTTC[C/T]TTTTAACACAAGAAA | 57626 |
rs533088317 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69798783 | TTAAGAGTTATACAC[A/T]GATGGCCTGGTGTGT | 57626 |
rs533097207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890471 | TGATGGGAAACCCAC[A/G]ACCCTGTGAGGAAGC | 57626 |
rs533100277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952707 | ACTTAGCATCCTTCA[A/G]CTGAGGGAGACAAAG | 57626 |
rs533109272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948938 | ATTGAAGAAGAAACA[A/G]TATCAATGTCACTCT | 57626 |
rs533112361 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758293 | AGCTAATTTTAATAA[A/T]CCTATAAACCAATTC | 57626 |
rs533118189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837815 | AAAGAAGTTTCTAAG[G/T]CTTTCCTTCTTCAAT | 57626 |
rs533123489 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033450 | GCCCACCACCACGCC[C/T]GGCTAATTTGTTTTT | 57626 |
rs533127684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826793 | TCATTAAATAATGTG[C/T]TCTTTTAAGAGAATA | 57626 |
rs533131715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737682 | GCTCACTAGAGGGGG[A/C]CTCCCCATGGGAATT | 57626 |
rs533144855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820298 | TATCGGTTATCATAA[C/T]GTATTCACTGTGAGT | 57626 |
rs533156344 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876752 | AAAAGAGATAAAAAA[A/T]ACCGGCCTGGAGCAG | 57626 |
rs533159338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033128 | GAATGGTTTATTTCC[A/C]ATTTTGGTAAACCTT | 57626 |
rs533188069 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69952104 | AGGTTCTAAATATGT[C/T]TTGTTTAACTGAATC | 57626 |
rs533188819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953465 | GAAAAGATGTCAAAA[G/T]GTCCATGGAAAAATT | 57626 |
rs533195379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826176 | AGCTGAGAATCTAGT[A/G]GTGAAGACTGGAGAA | 57626 |
rs533206537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091524 | TTCATTTATTTCTCT[C/T]GGGCAGCAAAATTTT | 57626 |
rs533218356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978634 | TGGGATTACAGGCAT[A/G]CACCACCATGCCCGG | 57626 |
rs533225964 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971797 | GAAAACTCTACAAGG[A/G]AAAACATTATGTTTT | 57626 |
rs533233542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009202 | AAGACAAACCAAGGA[C/G]AACAGTGTCGTAGTG | 57626 |
rs533241262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764274 | TGTCACCAATCAAGT[C/T]GTTTCCATACACTGT | 57626 |
rs533242422 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69862737 | ATATAGGAAGAGGAA[C/G]AGAGAGATCTCTCTC | 57626 |
rs533256497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743976 | TTTAAAGGGACTATT[A/T]CACATTTAAGTGGGG | 57626 |
rs533274213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924879 | GAAGCTGTTTGTGGG[A/G]CGCCTGGTCCAGCCA | 57626 |
rs533286600 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824580 | ATTAATTAAAAAGAA[A/G]ATAGGGATATGCACA | 57626 |
rs533314591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944907 | TGTATTTGATGTATA[C/G]CCCAAATGATATACA | 57626 |
rs533316498 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69777034 | TGGGTGGGAGGGACA[C/G]GGTGGGTGATAAATT | 57626 |
rs533324634 | in-del | -/TCTC | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099119 | TTTTACTTACACTAT[-/TCTC]TCTGATATAAACACA | 57626 |
rs533336965 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937910 | AAGAAATTTAAAAAT[G/T]TTGAAAGTGTTCCTT | 57626 |
rs533338292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912644 | TATATTGGGAGGTAG[A/C]AGGTGGCTGAGTTTG | 57626 |
rs533352014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871365 | TGCCTCCAGACTTTC[C/T]GAAATTACTTTTCCC | 57626 |
rs533353827 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995136 | CATTATTTATTTTTG[A/G]TTTCTTTTGACAACA | 57626 |
rs533354086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782697 | CCCACCACAGCTCAA[G/T]GAGGCCTGCCTGCCT | 57626 |
rs533356036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892022 | AAACATGCATGTATA[A/C]ATTATTAGAGTAGTA | 57626 |
rs533374760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960608 | TGTCCTCATCTACAT[C/T]TTCTGTTCATTTGGT | 57626 |
rs533398217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979286 | TTCAAGGTCATTAAT[C/T]TTTCAGATAAATGGT | 57626 |
rs533403807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918887 | GTTGTGTAATTCTCA[A/G]TTAGAGCTTCTTTAC | 57626 |
rs533404140 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069861 | TGGAAAAACAAGGAG[-/A]AAAAATGAGAGAAAG | 57626 |
rs533410380 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984368 | ATAGGAAAAGACTAC[C/T]TAGAGGCCAGGCATG | 57626 |
rs533413615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997414 | GATGTCTACAAGATG[G/T]TCATCTTGCATAACT | 57626 |
rs533415439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990349 | TGTAAATGGGATAAA[C/T]GTTCCAATTAAAAGG | 57626 |
rs533417269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788203 | GCTGCTATAAAGATA[C/T]ATGCACACATATGTT | 57626 |
rs533424449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944432 | TTTCTGATTGTGTTA[C/T]GTATTATTTTGCCGT | 57626 |
rs533426453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771598 | AGATTCACTTTAGCC[A/G]CTTCTAGTAAGAAGT | 57626 |
rs533442675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813624 | GTTCAAGGTGAGAAC[C/T]GAATCAAGAATCCCA | 57626 |
rs533447181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730917 | ATTGTAAGTTTTACT[A/G]TCCATGAATAGATAT | 57626 |
rs533447883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077883 | CTGGATATGTTCTGT[G/T]CCCTTTCTGTGATAT | 57626 |
rs533447971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085092 | AATATGGTGTATAAA[C/G]ACAAGTATCTGAGTG | 57626 |
rs533449331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762817 | TCTTGTGTGCACCCA[C/T]GGGGTATATCTTTAT | 57626 |
rs533449412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737407 | TGGCCTCGCTCCCAC[A/G]GAACCCCACAAGCTA | 57626 |
rs533451705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003656 | ATATTTAATTTTTAT[C/T]ATATTTGTTTATTTT | 57626 |
rs533466413 | snp | C/G | | | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970209 | TGTAAACATAACCCT[C/G]TATCTCAAATGCCTG | 57626 |
rs533471692 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69737205 | GAGGTCCCCTCATGA[G/T]CCCATACCACCAGGG | 57626 |
rs533483116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084282 | TATACTAAGTACTTT[A/G]TAACTATACCCAGCA | 57626 |
rs533485169 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70017957 | TAAAGGTTAAAGAAA[C/T]GTGAAAATAAGCGCT | 57626 |
rs533485601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028316 | TGCGGCCCATGGACA[A/G]CCAAAAATATGAAAG | 57626 |
rs533487280 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777787 | TATGTATAACTAACT[A/C]TTTATTTAAATTGTC | 57626 |
rs533488505 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886494 | TAATTATTGTTAATA[-/AT]ATATATATAAAACTC | 57626 |
rs533495043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804393 | CATCTATAATTCAAG[C/T]AAATAGCAACCTCAC | 57626 |
rs533513168 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803341 | TAATTACTTGCACAG[C/T]ATCTCTCAGTTAACA | 57626 |
rs533513847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045433 | TTATTTCCACATTTA[C/T]GGAAAAAATACCATC | 57626 |
rs533521830 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69932065 | CAAATTATTAATATG[C/T]GAAAGTACTTATTCA | 57626 |
rs533525663 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022423 | TGGAGTGAGAAAAAA[A/T]ATTATATACAAAACA | 57626 |
rs533526312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807270 | CTACCCTCTCCAGGC[C/T]CAAGATACTATTTTG | 57626 |
rs533540077 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048866 | TGCGGGTTGGGGACC[A/C]CTGCTATAAACAATA | 57626 |
rs533544892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979682 | TACAATGATCTGAAA[C/T]TCTTAACATTTGTCT | 57626 |
rs533549498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056752 | GAAATTAAGAGAGAA[A/C]TTTTTTAAATTTCAT | 57626 |
rs533550889 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69783086 | GGAGTGGACCTCTAG[A/C]AAATTCCAACAGACC | 57626 |
rs533554299 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70098860 | CAAGGCACCATGTAG[C/T]TTCAATGTGAATAAA | 57626 |
rs533554833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895394 | CAAGCTGCCACTGTC[A/C]TGGTGCGTCTCTCAC | 57626 |
rs533570858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897888 | ATTGATTTATCTGTA[C/T]CATTCCCTGTGGTTA | 57626 |
rs533579492 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075187 | GAAGAGATGTATGGA[A/T]TTGGGAGGCACACTT | 57626 |
rs533582959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101462 | AGACGAAGTCTCGCT[C/G]TTGTCCCCCAGGCTG | 57626 |
rs533586783 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779880 | CAATGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 57626 |
rs533587200 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062732 | ATTCTTGCTTCTTAA[A/T]GTATTAAACTTGTCT | 57626 |
rs533594880 | in-del | -/TCTC | 0.00240625 | 0.0346025 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837605 | ATATATACACATACA[-/TCTC]TCTCTCTATATATAT | 57626 |
rs533598094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104191 | TCTAATGTATATTTA[A/G]ACAGGGAAGTAGAGA | 57626 |
rs533602602 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69926468 | CGATTTCCTCATAAA[A/G]CATCTCATGTCCATA | 57626 |
rs533613604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984812 | GGTTTATATCAACCT[A/G]AAAACTTCTGTGCAG | 57626 |
rs533615237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69900558 | TTGTTGAGCAAGAGA[C/T]GCCGGGTTTTAGTGG | 57626 |
rs533619078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940909 | TTTATAGAACTTATC[C/T]TTGAAGTTTTATGGA | 57626 |
rs533619592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854753 | CACAAAATTATAATT[A/G]GTTCTTACATAGTCT | 57626 |
rs533622052 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814066 | CAGACAAATGGAAAA[A/G]AATAGAGACCCCTGA | 57626 |
rs533632310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858140 | GCATCTACCACAGGG[G/T]ACACCCAGAGACATT | 57626 |
rs533640740 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70095432 | TTTCAAAAATGACAC[A/G]CTAGAGGATTAAACT | 57626 |
rs533644536 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727624 | TTCTAGAATGAAGAA[A/C]CTGGAAATGACCATG | 57626 |
rs533647668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072714 | GATTATATCAATAGA[C/T]GCAGAAAAGCATGTG | 57626 |
rs533653232 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69808433 | GCCACTACACAAACC[C/T]TTCTGCAACTAAGGA | 57626 |
rs533669225 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69987803 | GGCAATATACACATA[A/G]ATATTTATACATATA | 57626 |
rs533690349 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69888933 | AGAGTAATTCCCTTA[A/G]GAAATACTAGCTTTC | 57626 |
rs533700037 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741807 | CTTTCTCAAGGACTC[A/G]GGAGCTGCAGTTCCT | 57626 |
rs533700096 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749672 | AAGATGTTGGCCTTC[A/G]AATATGGAGAAGGAA | 57626 |
rs533712345 | in-del | -/AA | 0.0617579 | 0.164514 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958739 | TCAAACCTTAAAATT[-/AA]AAAAAAAAAATACAT | 57626 |
rs533713180 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038647 | AGGGTGGAGTGTGCA[A/G]TGATGCGATCTCAGC | 57626 |
rs533721618 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69940670 | ACATTTATAAATGCA[A/T]ATGTTACAGGTTGGT | 57626 |
rs533746021 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945096 | GTTCAAGTGATTCTC[C/T]TGCCTCAGCCTCCCA | 57626 |
rs533759402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69836338 | GGCGTTTGCTGATTT[C/T]GAAGATGTACACAGC | 57626 |
rs533760441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969891 | ACCACACTAGAAAAT[C/T]TCTTATTGAGGTCAC | 57626 |
rs533772659 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923204 | AATTCAAGGTCAGGG[A/G]AACCCTCAAATAGAT | 57626 |
rs533789680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717016 | TAAAGTCCTCATTCT[C/T]ATTCAGTCCCTGCCT | 57626 |
rs533790270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019184 | ATCTAATTCAGGAAA[G/T]GTTGTCTCTGTGTTA | 57626 |
rs533794887 | in-del | -/GTGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69730295 | TGTGTGTGTGTGTGT[-/GTGT]TTTCATTACAAAATA | 57626 |
rs533798579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710695 | AATCTACAGATGTAT[A/C]AGCATTGTCCAAACA | 57626 |
rs533819436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055854 | CAAGAAATTAAATCA[C/T]ACTACCAGATAAAAA | 57626 |
rs533825830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728500 | GCTCACTGCAGCCTC[C/T]GCTTCCCAGGTTCCA | 57626 |
rs533827587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981616 | TTAGATTATATTTGC[A/G]TTAGAGTTATATGTA | 57626 |
rs533831724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802939 | TAAAAAGTATTTATA[A/C]GGCTGGTCTGAGTGC | 57626 |
rs533832343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755900 | CAGCCTAATCACTTA[C/T]TAGCTGTGGGATTTT | 57626 |
rs533834449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929212 | ATGATAAACACATCA[A/G]GTGAGCTACTCAAAG | 57626 |
rs533839902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70106878 | AACGACTGATATAAT[C/T]TAATGACGGTAGATG | 57626 |
rs533841544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775140 | ACTAATAGATAAGAC[A/T]CTACTACAGGCAGGA | 57626 |
rs533845786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768253 | TTCTAGATTGTATTA[A/G]AAGAATTTAGAGTAT | 57626 |
rs533850617 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716406 | GCACCTAGTTTAGTG[A/G]AAAAAAAAATGATGT | 57626 |
rs533858093 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062119 | GTTACCTTTCCCATC[C/T]GCTAGGTATCTGATT | 57626 |
rs533873592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014004 | GCTAATAAAAGCGTT[G/T]CTGGAAAACAAATTT | 57626 |
rs533876820 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69795883 | ACGTTTATTGTCCTC[A/T]TCCCCACAGATTTTT | 57626 |
rs533876828 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69784709 | AGTGACCTACAAAGA[A/G]ACTTAGACTCCCACA | 57626 |
rs533890600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762163 | TCTTCAGCAACAGAA[A/G]TACTTACTTCCCTAG | 57626 |
rs533893114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69981184 | ATACATACTTCCTTG[A/T]ATTTCTCTGGCAGTA | 57626 |
rs533896104 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70007459 | CAAAAAAAAAAACAC[A/G]AGTAAACTTATTAAA | 57626 |
rs533908511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729203 | TTTCTTTATTCACCA[A/G]GTGAGTCTGGCTGTG | 57626 |
rs533918750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902264 | TTCTTTCATGTTTGT[A/T]CAACATGGGCTGGTC | 57626 |
rs533958635 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031921 | CTATTATGAGTCAAA[A/G]TACCTAGAGTTTCCA | 57626 |
rs533964213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703789 | TCATTACGGTAACAT[A/C]CTTATATAGCTTTGT | 57626 |
rs533978812 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779273 | AATGAGGGTTTTCCT[-/AA]AAGTTTTACAATTTA | 57626 |
rs533980111 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69729163 | GCACCACACATCGAC[A/G]TTTATTCACTTTTTT | 57626 |
rs533980448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711098 | AATTTTTCAAGCATT[A/G]GTGTCATTTTCATAC | 57626 |
rs533985019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037102 | AATCACTGTTGATTG[C/T]TGTAATGCCAATTTT | 57626 |
rs533993295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037717 | GTTGTGTTCCATGAA[A/G]TAGATTCATAACTAT | 57626 |
rs533995306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781843 | TTCTCTACTATAATG[A/G]CTATAAATGGGATAT | 57626 |
rs534001580 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69735301 | CACTATAAAGGTTTT[-/C]CAATTAAAATAGGTA | 57626 |
rs534009383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791274 | AATTTAGCAAAATAG[A/G]TACAAGACTAGGGAC | 57626 |
rs534012676 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69829684 | ACAAGGTAAAAAAAT[G/T]AAAGAGCTGTGAGGC | 57626 |
rs534018557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090030 | CCCATTTAATCAATA[A/G]TATTGATAATAGAAT | 57626 |
rs534020602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076683 | CTTTCTCTCTGTAAA[A/C]GAATCAGCAGAATGT | 57626 |
rs534033949 | in-del | -/GCGGCGCTTGCAGTGAGCAGAGATC | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797758 | GCATGAACCCGGGAG[-/GCGGCGCTTGCAGTGAGCAGAGATC]GCGGCGCTTGCAGTG | 57626 |
rs534034712 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70056850 | AAATTTTATTTTAAT[A/G]AACAACTGCATTTAA | 57626 |
rs534050644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075975 | CTACAAAACTCTGAG[G/T]ACAAATATCAAAGCT | 57626 |
rs534057844 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884463 | TACGTGAAGCTAAAG[A/G]TGTTCTGAGGAATCT | 57626 |
rs534058399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69964313 | TACAAAAGTATTGGG[A/G]TTATGGGCATGAGAC | 57626 |
rs534059481 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69787321 | ACAGAAATATAGATC[A/C]ATGGAACAGAACAGA | 57626 |
rs534086790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882850 | TAAAAGCTTGACTAT[A/G]TATGTAGACATATAT | 57626 |
rs534087129 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890646 | CTTCCACACACACAC[A/G]CACACACACACACAC | 57626 |
rs534095440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928731 | ATCAATTGAATATCT[A/T]TATAGATGAAGGTAG | 57626 |
rs534098570 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69818109 | CTTTTCATCTGACAG[A/C]CTTATTTTATTCTTG | 57626 |
rs534102850 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015524 | TTTGACAGTGCAAAA[A/G]CAATGCATATTTAGC | 57626 |
rs534104308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881613 | AAAGATACAAGACTC[A/C]GAATCAGAGAGAACT | 57626 |
rs534104491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69889071 | ATATAATTTTCTATT[G/T]CTTTTTAGAATTTAA | 57626 |
rs534105446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971967 | TATCCAAGTGATCAA[C/G]AAAACAAAAGTTTTT | 57626 |
rs534111415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843142 | AGCAGAGTAGGGTGA[C/T]TATACCTAACAAAAA | 57626 |
rs534121810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102680 | AGTCTGTGATTCTAG[G/T]AAAATTAATTACCCT | 57626 |
rs534121927 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69790806 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA | 57626 |
rs534127752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051381 | GCCTTCAGCTTTTCA[C/G]GTTTTACATGCAATG | 57626 |
rs534132147 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770862 | CAAACAATTCTGCCT[C/T]AGCCTCCCAAGTAGC | 57626 |
rs534135857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763931 | AACCTGAAGTAACCA[A/T]TTTTTTTTCTATTGT | 57626 |
rs534148264 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850925 | CTTTTGAACTATCTG[-/A]CTGACTCCTAGTTTT | 57626 |
rs534159377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818680 | CTTTGTGTGTGAAAT[A/G]GAACTGAGCTTTGGC | 57626 |
rs534166271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026308 | AAATTAATACTACTG[C/T]ACCCATTGTTTTTAG | 57626 |
rs534171215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890115 | GGGGACAGTATAGTA[C/T]TATAAAATAATTACA | 57626 |
rs534171842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805111 | CACAAATAAAAGTCT[C/T]TATTTTTTTAAGTAA | 57626 |
rs534191500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896399 | AGTACCTACACAGTA[A/G]TAGCTAGATAAGTAT | 57626 |
rs534196585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064293 | AATATAATCTCAGCC[A/G]AAACATACAAATTTT | 57626 |
rs534197249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69818013 | CCACCCTCAGAAGAG[A/G]CCCCAGAAATATTTA | 57626 |
rs534209275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824648 | AAATCTTAGATAAAA[A/G]ACTACAAAATGTGTG | 57626 |
rs534215165 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107841 | AGAAGACGCTAGGTG[G/T]GCTGCGCGCTCTGCC | 57626 |
rs534220449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053771 | CCAGACTAATTGCCT[A/G]CACTTGTTTATGCTT | 57626 |
rs534222317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834199 | CTAAAGAACTTATCT[A/G]TGTAAACCAAACACA | 57626 |
rs534224402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910321 | TACAAATCTAGACAC[A/C]ACTCTGTAGAATGGT | 57626 |
rs534232775 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054846 | AGAATTAGTGAGCTT[-/G]GAGACAAGTTATTTG | 57626 |
rs534233070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063521 | ATTTTGTTATTTAAA[A/G]TTATAATCTAACACA | 57626 |
rs534239179 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982803 | AAGAGGGTCATTATA[C/T]GATGATAAAGGGGTC | 57626 |
rs534242566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786893 | CGAATCATGAGGGAA[A/C]TCCCATTCACAATTG | 57626 |
rs534254629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69769936 | GGGCGGTGACATGCT[A/C]CTGTTTGCCAGACTA | 57626 |
rs534255310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031551 | ATATTGTTAAAGACA[A/G]ATGGGGTCTAAAATT | 57626 |
rs534280015 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996076 | TTGGGAGGTCAATGC[A/G]GGAGGATCATGAGGT | 57626 |
rs534282052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003254 | TTCCTTGAAACATGA[C/T]GAAAACTTTGATGAA | 57626 |
rs534282611 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69706179 | ACATACAGTGCTCTC[C/T]GAATAAGAAATGCTT | 57626 |
rs534300669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916520 | CCACATGTTCTCACT[C/T]ATAGGTGGGAATTGA | 57626 |
rs534315520 | in-del | -/ATTTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69715525 | GCAGTTTTATTATTT[-/ATTTT]TTTTTTTTTGAGACG | 57626 |
rs534322254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994690 | AATGAATTGGTATGG[G/T]TCTACTTACCAAGAA | 57626 |
rs534333587 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757372 | AAAATATATCAAGAC[-/AT]ATTCAAATTTTAGGA | 57626 |
rs534351135 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69853770 | TTTCCTAGATATAAC[C/T]GGATAAGGTATGTTG | 57626 |
rs534355283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876915 | GGTGGCGCATGCATG[C/T]AATCCCAGCTACTCA | 57626 |
rs534356063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929850 | AAAACAATGGCAACT[C/G]TTGATTACCATATAT | 57626 |
rs534359792 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805982 | GATATTAAAAAGTAT[A/G]TAACTATAGCGTTTT | 57626 |
rs534379924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097246 | AAATGTGAGTCCTAT[A/G]AGGCATTTGCTATAT | 57626 |
rs534382516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961095 | TATTTAAGCCAGTTT[A/G]AATCATTTGTGGAAG | 57626 |
rs534396559 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69963746 | AAGAACATAAAATAT[A/G]TTTAAATTTACTGCC | 57626 |
rs534406472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750791 | AAAAAAATGTAATTT[A/G]TAGCATTTAGATATA | 57626 |
rs534407319 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896813 | AGCTGGGACTACAGG[C/T]GCACACCACCACCTC | 57626 |
rs534412811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002690 | GCATAAGTTGTTCAA[G/T]AAGTGATCTTAACAT | 57626 |
rs534417024 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091672 | TACATCAATTTTACA[A/T]GTTAGAACCTTTTTC | 57626 |
rs534431901 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69940957 | ACATTTTAATTAGTA[A/C]TTCAATGAGTTAGAT | 57626 |
rs534446736 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69811439 | AACATCCCTTCCTGA[A/T]AACAATCCTAAACAA | 57626 |
rs534458876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102120 | TCATTTTCAAAGTTG[A/G]TTATCCCCTTGACTG | 57626 |
rs534477431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69812183 | GTCATTCAGTAGCAG[G/T]TTGTTCAGTTTCCAT | 57626 |
rs534484089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813878 | CCAATGTTGTTTTTC[A/G]CAGACTTAGAAGAAC | 57626 |
rs534486034 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69768979 | GCTAGCAATATTTAG[A/G]AATTCATGGAAAGTT | 57626 |
rs534489993 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904752 | GGCTCCAGAGTTTAC[A/G/T]CTTAATCATTAAGTT | 57626 |
rs534497564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897556 | TGAGAAAATATTATT[A/C]AACCTAGCGAGGGAC | 57626 |
rs534502112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865232 | CTGAGCCAGTGCACT[C/T]GGCCCTGAGTTGAGC | 57626 |
rs534509873 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70030061 | ATCCTAAATATATAT[G/T]CACCCAATACAGGAT | 57626 |
rs534538755 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70091286 | TTGAACCCTTTCTTT[C/T]TATCTTTCTTCCCTT | 57626 |
rs534540106 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69958798 | ATTCCCACTCATTCA[-/T]TTTTTTTTCCTGTTT | 57626 |
rs534541841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027034 | TCAGGTGCATCACAA[C/T]GGGAAACAACAAATT | 57626 |
rs534542574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69776419 | GCTGTATGAACTTCA[A/G]CAAACTAATTAATCT | 57626 |
rs534543779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984148 | AACATATGTACAAAT[A/C]GACAAGCGGGAATGG | 57626 |
rs534549059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903831 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 57626 |
rs534559214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744114 | TCCTAGATATAATCA[G/T]TTAGGAAGATACTAT | 57626 |
rs534562088 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911896 | ATCTTCATTCCTAAT[G/T]ACTGCCCACATTATG | 57626 |
rs534568193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777253 | TTAAACCTCTTTTTC[A/T]TTTTAAATTATCCAT | 57626 |
rs534571696 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69722948 | GATAAATGGATAATG[C/G]AAATGTGCTCCATTT | 57626 |
rs534581100 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69992548 | ATCTACTTTGTAGAT[A/G]AGGAGACCAAAACAC | 57626 |
rs534582916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038820 | GGTCTCAAACTCCTG[A/G]CCTCAGGTGATCCAC | 57626 |
rs534591143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953187 | TGAAATTATGAATGC[A/G]CAAGTCTGAGGATAA | 57626 |
rs534598548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990588 | AAGGGCATTACATAA[C/T]GGTAAAGAGTTCAGT | 57626 |
rs534601345 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69960164 | GTGTTATCTTAGTGT[C/T]AGCAAATCCTTCTTC | 57626 |
rs534601637 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706157 | TACTTGCTTTTATTT[A/T]TTTTTTACATACAGT | 57626 |
rs534604442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959449 | GTTTCAGGTTGTATG[A/C]AAATTGAAATTGACC | 57626 |
rs534607684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69819922 | ATAATCTGTTATAAA[C/T]GCCTTTGTCAAAGTC | 57626 |
rs534615869 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69724179 | TGACCTGGAAGTCCC[C/T]AATTTTGCCTTGGAG | 57626 |
rs534621443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788359 | AGTTCACGTCCTTTG[G/T]AGGGACATGGATGAA | 57626 |
rs534622761 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038441 | CAATTGCTGGGTCAT[A/G]TGCTAAGAGTATATT | 57626 |
rs534631085 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782483 | CTGTGCTTTTCCAAC[A/G]GGCTTAAAAAATGGC | 57626 |
rs534635927 | snp | C/G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69866152 | CTTTTGAAAAGAGTA[C/G/T]AGCACTTATGCTGAA | 57626 |
rs534639230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925054 | TGGGATTCAGGCTGG[A/T]AGTGCAAGCTGGGGA | 57626 |
rs534646669 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976626 | AAATAACCTAAAATT[A/G]AATATTAATTAGATT | 57626 |
rs534661499 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044395 | GCCATTTCTTATCAC[C/T]GTACATTGTTTATTT | 57626 |
rs534662349 | in-del | -/TTGTT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69708296 | GTTTTGTTGTTGTTG[-/TTGTT]TTGTTTTGTTTTGTT | 57626 |
rs534674142 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052012 | CTTATTCTTAAATAC[A/G]AGAAATATTTTAGTA | 57626 |
rs534675198 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69952516 | ATGTAAGTGCCATTT[G/T]GCTAGGACATTTTCT | 57626 |
rs534680929 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010790 | CCAGCTACTAGGGAG[G/T]CTGAGGCAGGAGAAT | 57626 |
rs534693374 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046043 | CTTTCTCTAAAATGC[A/G]AAGTGGACATCATGT | 57626 |
rs534696701 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69805668 | AATTAGCAAGGTCAG[C/T]ACCAGCTCTAGATGA | 57626 |
rs534698756 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893360 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 57626 |
rs534700368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098296 | TTTAGAAAAGCTATA[A/G]GAGTGTCACATCTAT | 57626 |
rs534704009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757892 | AACTCAGGAGGCAGA[A/G]GTTGCAGTCAGCCAA | 57626 |
rs534713290 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69754417 | TTTGTATATACAAAT[A/G]TCCGAACTTACCATA | 57626 |
rs534734202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107021 | GTGAGGTGTCTGAAC[C/T]AATAGAAATTAATGA | 57626 |
rs534735713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719147 | AGTTGAAGGGAGGAA[A/G]CAAGGAATAAAAGAA | 57626 |
rs534747031 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69810679 | TAAAATAAATAAAAT[C/T]AGAAAACAACTAAAT | 57626 |
rs534748319 | in-del | -/TATAACTTCCAAATTT | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078439 | GAAAACCTTCATTTG[-/TATAACTTCCAAATTT]TCTCTTTAAATATTA | 57626 |
rs534762608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103932 | TAGAGATGCAAATCT[A/G]TAAAGACAGTTTATG | 57626 |
rs534764656 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787004 | ACTGCTCAATGAAAT[-/A]AAAGAGGATACAAAC | 57626 |
rs534765964 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69887620 | CGCTGGGATGCAAAC[A/C]CAATTCAGCTAAGTT | 57626 |
rs534790882 | in-del | -/CACACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70082364 | ACACACACACACACA[-/CACACA]AAGGAACCATAGTAG | 57626 |
rs534791744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69891250 | CTTTATTAATTCTAT[A/G]GCACCCACTAAGTGG | 57626 |
rs534807124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777887 | TCTGAGTATTATAGT[G/T]TGCATTTTACTGGTA | 57626 |
rs534822372 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033771 | ATTACAGGCACGCAC[A/C]ACCACAGCCGGCTAA | 57626 |
rs534822501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820351 | ACTACTAACTCTTCA[A/G]TCCACAAGTCATTAC | 57626 |
rs534829021 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69779742 | GCTGGAAGTGAAGAT[A/G]GTAAAGTTATCTGCT | 57626 |
rs534830769 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093122 | ATAAGCTATATGATG[C/T]GCTATTATGTAATTA | 57626 |
rs534836562 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744059 | GGTATATGTAAAAGT[G/T]TTGGAGTTATCAGCA | 57626 |
rs534836899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022065 | TGCCAAACCCAAAGT[A/C]ACTTTGATTTTCTCC | 57626 |
rs534839947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69937655 | CACTTCTACCTGATG[C/T]TGAGCTCGCAATCAA | 57626 |
rs534841247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737840 | GTAAGGGCAGCCCAG[A/G]CGAGGGGGATTTTCC | 57626 |
rs534858081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065141 | AGTGATACTTGAATA[C/T]TGGCCTAACCACAGT | 57626 |
rs534860178 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70048220 | CAAGAAATGGGAACT[C/T]TGAAAATCCTGAACG | 57626 |
rs534860420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072372 | AATAGTTAAGGTAGA[A/C]ATGATGCCATTTTTC | 57626 |
rs534864295 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70065596 | CAGCAGCAATTACCA[A/T]TTAACACAAAATTTT | 57626 |
rs534867269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719871 | TGCAAAAATAAGTAA[C/T]ATTAGTATATTAGTT | 57626 |
rs534868148 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69986921 | TAATAGTGATATTTT[A/C]ATAATAGACAAGAAG | 57626 |
rs534877439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722947 | GGATAAATGGATAAT[A/G]GAAATGTGCTCCATT | 57626 |
rs534877444 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70016129 | TCAAAAACATAGGCC[A/G]GTACTAATCAATCTT | 57626 |
rs534884689 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034541 | ATGCATCACTGGCTG[G/T]ATCAGATCAGAAGCA | 57626 |
rs534887533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864697 | ATAAGCAATTGTTTT[A/C]AAAAATCCTTTACAT | 57626 |
rs534908254 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040391 | GGATCATTAGAAGCA[C/T]AAACCTCAGCATCAT | 57626 |
rs534911929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826457 | TAGTGGTGGGCACCT[A/G]TAATCCCAGCTACTC | 57626 |
rs534913449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69744946 | TGTACACTTTCTTGA[C/T]GTACATATGAGTTCA | 57626 |
rs534923739 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69849477 | TTAAGCCAAGCACAT[C/T]TATGCTCTCTTTCTC | 57626 |
rs534942790 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871833 | TGGCTTTTCTTGTCT[A/G]TATTTCTATCAGCAT | 57626 |
rs534943429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833100 | AACAACAAAGATAAA[C/T]AGATAGGCCTTAATT | 57626 |
rs534956276 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867914 | GTTAAATAACGAGTT[A/G]ATGGGTGCAGCACAC | 57626 |
rs534964911 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69987637 | AAGGACTACTAAAGA[A/C]CTCTTTTCCATTGTT | 57626 |
rs534976189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926679 | CAGGCCGGGCGCGGT[A/G]GCTCAAGCCTGTAAT | 57626 |
rs534988234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926100 | ATTATCCCAATAAAC[A/G]TTTCTAGTTTTTTAT | 57626 |
rs534997093 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919816 | CAAAAAGTAAAAAAT[A/T]AAAATAAAAAAGGTC | 57626 |
rs535000253 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70071270 | TTAGAAGATATAAAG[A/T]GCAGCACTACATGAT | 57626 |
rs535001459 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70101210 | GTACCATAGAAAGGC[G/T]AATCATACAGTTTAC | 57626 |
rs535026974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69765952 | GGATTTTACTCTTAG[C/T]CTCAGTTGACTAACA | 57626 |
rs535028321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838717 | ACAAATTGTTTGGCT[C/T]GTGTTAAGTGATTCA | 57626 |
rs535038307 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009372 | TAGGTGTTGCATAGG[C/T]AAAGGGCAGGGAAGA | 57626 |
rs535041659 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70085263 | GGAAAAGAGTTATTA[C/T]ACAATTAGGTTATAG | 57626 |
rs535044661 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935287 | ACTTGGTACATAGCA[C/G]TCAATAGTCACTATA | 57626 |
rs535046088 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908556 | ACGTAAAAACCACTT[A/T]CACTAAAATATAAAA | 57626 |
rs535058821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876333 | GTCCGTATGTCACTG[A/G]TATCTGATCAATAGT | 57626 |
rs535073389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979403 | ACCTTATACTTAATA[C/T]AGAATTTTAATATGA | 57626 |
rs535073723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792362 | AAACCCACAATGAGA[C/T]ACTACTTCAAATATA | 57626 |
rs535081357 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096715 | ATTTTCTCTTTTTTT[C/T]TTTTTGCTGCCAGAA | 57626 |
rs535083166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898000 | GGAAAAAGTAGTCAT[A/G]GTCAAATCAGCAAAG | 57626 |
rs535086603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772512 | TCTAAACAAATTAAG[C/G]CTGTTTATTATTTCT | 57626 |
rs535093814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044238 | CCCACGTACATGCAC[C/T]TCACTTGCTCTTCAC | 57626 |
rs535094030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938040 | AAGGAGAAAAAAAAA[A/C]ACACACAATATGTTT | 57626 |
rs535109732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69923853 | CAGGCGCAGCTGCAG[C/G]TGCCCAAGCTGCAGC | 57626 |
rs535109787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799257 | CAACTGTACTTCCCA[C/T]AGACTCCAAAGCCTT | 57626 |
rs535111767 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890865 | AGATATTTTTTGACT[A/C/G]TATATTGCTTCTTTG | 57626 |
rs535119170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724699 | TCAACAAAAAATCTT[C/G]ATTAAAGCCATACAT | 57626 |
rs535122622 | in-del | -/AA | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936072 | AGAGCTAATGCCATG[-/AA]AAGTTTAAAGATATT | 57626 |
rs535129785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837327 | AATAATAGGGTTAAG[C/T]TCAAGTAAACTGTGA | 57626 |
rs535132296 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70008707 | AACAATTGATCATTT[A/G]TATTTTTGTAGAGAC | 57626 |
rs535135081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984559 | ACCAATCTTTGGGCT[C/G]TATGTAAATCAGATA | 57626 |
rs535138525 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70102636 | TGGAGTCAGATACAA[C/G]GGGTTAAAGTCCAGC | 57626 |
rs535142435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096041 | CATTCGTTTTTATAA[C/G]CAAATAATGCTTTAT | 57626 |
rs535147083 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70028841 | AATTAGCCAAGCTTG[G/T]TGGCACATACCTGTA | 57626 |
rs535156834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69890055 | GGAATATATAAATTT[A/T]AAAAAAGAAAGGCTC | 57626 |
rs535171332 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69971326 | TCATCATCATTATCA[C/T]TGACTCAGTTGTTAT | 57626 |
rs535186091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086564 | GGTGACAGAGGGAAG[A/C]TCTGTCTCAAAAAAA | 57626 |
rs535192195 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929811 | AATAAAATTCTGATA[C/T]ACATTACATTGCCTT | 57626 |
rs535209805 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700787 | TTCTTTCTAGCAATA[A/G]TCATAAACACTCCAA | 57626 |
rs535222263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961564 | AATTAATGCATTTTA[C/T]TTATTGCCTCATGAG | 57626 |
rs535228231 | in-del | -/ATCT | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859947 | CAACAGAAAAACTCA[-/ATCT]ATCATCTGAAGGCCT | 57626 |
rs535234162 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69844662 | GTACAATTTGATCAT[A/C]ATTTTATTATGAGTA | 57626 |
rs535236710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861474 | GTTCATGATTTCATA[C/T]TGATGTTTATCAGCT | 57626 |
rs535248394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920295 | ATTACTATAATCTTA[C/T]AGCATCATTTTAAAA | 57626 |
rs535256640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027242 | TCTCCTTTACAAACA[C/T]TATATTCCTGAGCAC | 57626 |
rs535267023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879108 | GCCTGTCGTAGGAGA[C/T]ACGAGTTGATGGGTG | 57626 |
rs535287695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908543 | ATTTGAAGAGAAAAC[A/G]TAAAAACCACTTTCA | 57626 |
rs535292091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967752 | TAGATGGGCGTGGTG[G/T]CGCGTGCCTGTAATC | 57626 |
rs535297682 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69858554 | GTTGTTGAAATGAAC[A/G]TTTATCATGTTCCTG | 57626 |
rs535299745 | in-del | -/T | 0.0768147 | 0.180297 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728130 | TAAACAGCAATTTCT[-/T]TTTTTTTCTTTCTTT | 57626 |
rs535303129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092897 | TACAGTATTGAACAG[C/T]GCAGCCATGAAATAA | 57626 |
rs535309839 | snp | A/G | | | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700879 | GGAGTTCAACATGCA[A/G]TGGATATATATATCA | 57626 |
rs535312934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753078 | CTGAGATTCTTCCTG[C/T]CCAATCCTCCTTCCT | 57626 |
rs535321544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759998 | CAGTGTACATAGGCA[A/G]AAAGACACCCTCACG | 57626 |
rs535322444 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69885582 | GTGTTATTGCTAAAA[A/G]AGAAAATATCAATTC | 57626 |
rs535322620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705922 | ATATGTATTCAGATA[A/T]TATATTACATCATTT | 57626 |
rs535334051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989902 | TAGAATCATGTAACT[C/T]GTAAACAGGGATAGT | 57626 |
rs535341538 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038414 | GTTTTTACTGATAAA[C/T]GTCCTGGAGGGCAAT | 57626 |
rs535345098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957079 | TTTAACTTCACCCTG[C/T]CAAATCAAAGGCTTA | 57626 |
rs535347021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782308 | AGGGAGTGCCAGACA[A/G]TGGGCGCAGGTCAGT | 57626 |
rs535361321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885745 | GTTTATCAAAACCCT[A/G]ATATATGGCCCTGAT | 57626 |
rs535362160 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69904929 | GCATTTTCTACAATA[A/G]TAATATGCCTTAATA | 57626 |
rs535364373 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792939 | GGATGACAAAAATGT[C/T]TTGGAATTTGCTAGT | 57626 |
rs535383061 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69883523 | TGTGTAGTGGGTGTA[C/T]CCCTGCCACAGCAGA | 57626 |
rs535383961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69705249 | CACAAAAAATAAGCT[C/T]GGTGTTCAATGACAA | 57626 |
rs535392638 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70043249 | AATACTAAAAAAAAA[-/T]AAAAATAAAAATGAG | 57626 |
rs535401698 | in-del | -/TATT | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919837 | AAAAAAGGTCACATA[-/TATT]TATTTCAGTTCTGAC | 57626 |
rs535406215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787033 | ACAAATGGAAGAACA[C/T]TCCATGCTCATGGGT | 57626 |
rs535409864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083601 | AAGATATCAAACAGG[G/T]TATATGCTGTCTAAA | 57626 |
rs535420259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831225 | CAAGAAAAGAAGAGA[G/T]AAGATCAAAATAGGC | 57626 |
rs535422018 | in-del | -/AAAT | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782094 | CTACTTGGAGATGCC[-/AAAT]AAATAAATTTGTGTT | 57626 |
rs535423144 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70025687 | ACTATTTTTACTATA[C/T]ATATTATATATAGTA | 57626 |
rs535430148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724669 | TAGAATTTATACCTA[C/G]GATGCAAGGATAGTT | 57626 |
rs535454990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016096 | AAAGCATTCATCTCT[A/C]TATGAGAAAGAACAC | 57626 |
rs535462765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757454 | ACTCAAAGGTTAAGC[A/C]TCATGTATTATTTGA | 57626 |
rs535465165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973044 | TTAGGATTTCCTTCA[A/G]GGCCTAAAGCACAAA | 57626 |
rs535477001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062764 | TGTGGACAAGCATAC[C/T]ATTTTTATCAGTTTC | 57626 |
rs535478205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717812 | TATAAAAGCATAAAC[C/T]TATTTATTAGGACTC | 57626 |
rs535489465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764768 | ATTCTGAATTTTAAG[A/G]AGATTCCAAGGTAAT | 57626 |
rs535490055 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724253 | ATGGTTGATGTATTA[C/T]GTCTCCATAAAATGT | 57626 |
rs535493319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843050 | AGGGTGAGTGGGAGA[C/T]ATGGAGAACAAGGAA | 57626 |
rs535506174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715590 | CAGTGGCGCGATCTC[A/G]GCTCACTCTAAGGCA | 57626 |
rs535506757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70058261 | AGACAATAAAGAATA[C/T]GCAAATTAGAAAGGA | 57626 |
rs535509780 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69860160 | ACACAAAATATATGT[A/T]AAGTGTCTATTAATC | 57626 |
rs535510896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050766 | AACAAAAATATAACA[C/T]GTTTTTATGAGAGCA | 57626 |
rs535514845 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059143 | CAGGACATGGGAATG[A/G/T]ACAAATATTTCTTCT | 57626 |
rs535521985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806319 | CAAGACATAGTTTAA[A/G]TTACCTTCCAGGATA | 57626 |
rs535522013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059461 | GAGCATGAGCCACCA[C/T]GCCTGGCTGGGCAAA | 57626 |
rs535525006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015443 | ATTGTTATGCAGCAC[C/G]TAACTGTGCATGCAC | 57626 |
rs535528235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756722 | GATTCCATGATGTGG[C/G]CTCTGTGGTGTTCTC | 57626 |
rs535532285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820321 | CTGTGAGTAATTACA[C/T]TAAGCAGAAATTTTA | 57626 |
rs535539517 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70082874 | AAATTAGCATAGAAA[C/T]AGAAAACAAAATACT | 57626 |
rs535539838 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70061526 | TTTCCCTTTATCCAA[A/G]GACTTGGATCCTCAA | 57626 |
rs535542975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850684 | GAATTCAAACTACTC[C/T]CACAGCGTCCTAAAA | 57626 |
rs535548900 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730567 | ATTTACATCCAAGAG[A/G]ACATCCATTCCTTTT | 57626 |
rs535549914 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70057752 | CTGCAGTCCGCAGTC[C/T]GGCCTGGGCGACAGA | 57626 |
rs535551895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723802 | CCCAGACATTCCTTT[C/T]GGCTGATAATAACTC | 57626 |
rs535556541 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813331 | GCCTGTTGTGGGGTG[C/G]GGGGAGAGGGGAGGG | 57626 |
rs535569804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717113 | TTGATAAACATTATA[A/T]AACTGTATTTAACAC | 57626 |
rs535571351 | in-del | -/TGA | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867425 | CTCTTTTGTCACACC[-/TGA]TGAGAATAAGAAAGC | 57626 |
rs535579092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69857200 | GTATTTTATGCTGCA[C/T]TGAATTTGCTCCCTT | 57626 |
rs535582633 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842545 | ACAAAAAATAACATG[A/T]TGGTGTGAATGAGGA | 57626 |
rs535584112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770223 | GCCAGTCTTGGCATG[A/C]CTGGTCCAGATGTGG | 57626 |
rs535587626 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69987344 | AGAAAACTATTTTCT[C/T]GCAGCAATTACTTTG | 57626 |
rs535593092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953607 | AGGACCAATTAAGAT[A/G]AAATATGATAAAATC | 57626 |
rs535596371 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077956 | TATTAAATAAAAGGT[C/G]AAGTAAAATTCAGTC | 57626 |
rs535598234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070781 | TGATAATGATGTTAT[A/T]AGTAACAGGAGAAAG | 57626 |
rs535599251 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027778 | AGCCTCTGAGATTTG[C/G]GGATTTATTAAGTAG | 57626 |
rs535599449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943187 | GTGTGTCCCATTTTT[G/T]GTGGCTTTGAGTGTC | 57626 |
rs535599678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027813 | ATCACTGAACAAGCT[A/G]ACTATAGATAACCTG | 57626 |
rs535600068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902946 | ATACCATAGCTTTTC[C/T]ATTATATATATAATG | 57626 |
rs535609834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752961 | ACTATGCATGGTGGA[A/G]TTACTAATGCAGGCC | 57626 |
rs535626444 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69799915 | GGCATTAAATTCTCA[C/T]AGGAGCGCAAACCCT | 57626 |
rs535630112 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780298 | TTAAAATGTTTGATA[C/T]CTTGTATTGAGTGGA | 57626 |
rs535633750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863722 | TGTCTATTGGATGAT[A/G]CAAAAAACAGATTCA | 57626 |
rs535637101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782435 | AGGGGTGACAGACGG[C/T]ACCTGGAAAATCGGG | 57626 |
rs535651587 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70092533 | TACTTTATAGCACAC[A/G]GCTTTTATATTATTA | 57626 |
rs535652494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961111 | AATCATTTGTGGAAG[A/G]ACGAAATGTATATGT | 57626 |
rs535655225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788503 | ACATCACACTTCGGG[C/G]ACTGTTGTGGGGTCA | 57626 |
rs535658222 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69982252 | CAGCCTGGGCAACAC[A/G]GTGAAACCCTGTCTC | 57626 |
rs535674471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752341 | CTATGTTTGATTTAT[C/G]TAAGCAATTAAAAAT | 57626 |
rs535676645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838702 | TTCTCAATATATCCA[A/G]CAAATTGTTTGGCTT | 57626 |
rs535678162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870639 | ACAAAATAAAAATAT[A/G]TATATATTATTTATT | 57626 |
rs535685416 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69874288 | GACTATATAGTCCTC[C/T]TCCCTTATCTCTCTA | 57626 |
rs535694568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832634 | AAGAGCCTGCCTAGC[C/T]AAAGCAAGACTAAAC | 57626 |
rs535698737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801063 | TTCGGGTGATGACTA[C/T]CTAAAGCCCTCGATG | 57626 |
rs535701028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787595 | CATTCAGGACATAGG[C/T]ATGGGCAAGGACTTC | 57626 |
rs535709531 | in-del | -/CTG | 0.0581099 | 0.160244 | intron-variant | KLHL1 | GRCh38.p7 | 13:69783696 | AGACCAAATCTACGT[-/CTG]ATTGATTGGTGTACC | 57626 |
rs535717881 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053271 | AGGAAATATAACAGA[A/T]TTGAGGGAATCTTAA | 57626 |
rs535728705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084410 | AGCATGAAATATATT[C/T]CTGCTTCATTATTGA | 57626 |
rs535736067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077558 | GAAAATACATAAAAC[C/T]GTATTTCTCAAAGTG | 57626 |
rs535750167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924482 | TCACCCCTTCTGAGA[G/T]CTGAACACTCATTGG | 57626 |
rs535761544 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870167 | TTTACAAGAGGCATG[A/G]CATGAGCATCTGCTT | 57626 |
rs535766269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925233 | TTCATAATTTGAATT[C/G]TAGCTCCAACACTCA | 57626 |
rs535776487 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931420 | CCCAAATTAACTTTG[G/T]CTTGCATAAAACATG | 57626 |
rs535785022 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69855656 | CCTTCCTGCCGCCTC[A/G]TAAAGAAGGTCCCTG | 57626 |
rs535795574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806956 | GACACAAGTGGACCA[C/T]ACACTCCACAGCTTC | 57626 |
rs535813051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69891201 | ATTACCTAGATACAA[C/G]TCTGCCGGACTGAAG | 57626 |
rs535814477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022010 | TCTCATTTATCAATT[A/T]TTTCAGAGATCATTC | 57626 |
rs535827960 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69981239 | TAAAATTACACTAAA[C/T]ATAGTAAATAAAATA | 57626 |
rs535833870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979348 | ATTTCCTCACATATC[A/G]TTTCATGATCTAAGA | 57626 |
rs535862638 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772031 | GTCTTGGCTCACTGC[A/T]ACCTCTGCCTCCTGG | 57626 |
rs535878714 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097441 | TAAAGAAAAGAACCA[G/T]CTGTCTAACATCACC | 57626 |
rs535878727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103841 | TATTTGACTGGACTC[C/T]ATGACATCTATCAAA | 57626 |
rs535882066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065580 | TGGAAAAGACATCTT[G/T]CAGCAGCAATTACCA | 57626 |
rs535893176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073143 | CTATTCACGATAGCA[G/T]ACTTGGAACCAACCC | 57626 |
rs535895027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978772 | GATTACAGGCGTGAG[C/T]CACTGTGCCTGGCCT | 57626 |
rs535897028 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69982975 | CCTTAAAGAGTCCAC[C/T]TAAAATCTGTTAGAA | 57626 |
rs535905710 | in-del | -/A | 0.458392 | 0.138104 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959558 | TCAGACTACTCATTA[-/A]AAAAAAAAAAACATG | 57626 |
rs535906357 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903782 | GAGTAGCTGGGATTA[C/G]AGGTGCGTACCACCA | 57626 |
rs535908204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904910 | TCTGTTGATTCCCAT[A/G]ACTGCATTTTCTACA | 57626 |
rs535913909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896938 | GCCTCCCAATGTGCC[A/G]GGATTACAGGTGTGA | 57626 |
rs535927226 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777806 | ATTTAAATTGTCCAT[G/T]AACTAATCTGGACTT | 57626 |
rs535947989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991363 | AAAAGAACAGATCTA[A/G]GAGTTGGTTCTTTGA | 57626 |
rs535950815 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69990523 | AGGAGCTGTAATCCT[A/G]ATTTCAAGCACAAAA | 57626 |
rs535966909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078882 | AAAGTGAATATGTTG[A/C]AATGAACCCACTTAA | 57626 |
rs535968559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071540 | TCTTCTCAAGCTCAC[A/G]TGAAACACTCACCAA | 57626 |
rs535972542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983682 | TATGACAGGAGGGTC[A/G]CTTGAGCCCAGGAGT | 57626 |
rs535979097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961546 | TCAATCTATTGATCA[A/G]TCAATTAATGCATTT | 57626 |
rs536018251 | in-del | -/CT | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911134 | CTCTCTTCTGTCTCC[-/CT]CTTTCTCTTTAATTC | 57626 |
rs536022591 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69997128 | CTGGAGATTGAGGCA[C/T]GAGAATCACTTGAAA | 57626 |
rs536026453 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894048 | AGGAAATCTCCCAAC[A/C/T]GTTTTCCTGATGGCA | 57626 |
rs536043305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69707137 | AGGTTAGTTTCTGTT[A/T]ATGGCTGTGGGGATT | 57626 |
rs536067286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099717 | ATAACATTTTTTCAT[C/T]TAATCGTAGTTTAAT | 57626 |
rs536068612 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69900817 | GTTTAGAAGGCATCT[A/G]TCCTTATTAAACTAC | 57626 |
rs536075020 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056307 | AATTGTAAATATATA[C/T]GCACTGAATACTGGG | 57626 |
rs536086398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69794105 | ACCTTCTCATTTAAG[C/T]TACCAGCTCTAAGGT | 57626 |
rs536099530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985892 | GTGTGTGTATGTATA[G/T]AAGTATATATATGTA | 57626 |
rs536102517 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69978415 | ATTAATTTAAATAGG[G/T]TTTGGGATAAAAGCT | 57626 |
rs536106284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899352 | AATGCTGGGAAAAGA[A/T]AGAAGCTACTCTCAT | 57626 |
rs536108404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104547 | AAAACTAAATGAATA[A/T]AGAGAAGATCAATAA | 57626 |
rs536119214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098107 | AGTTTCATTAACTCT[G/T]GTATTATAGATCATA | 57626 |
rs536128404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758942 | AAAATAAGTTTGAAA[C/T]GATGACACAGGTACC | 57626 |
rs536134966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060659 | GACCAGCCTGGCCAA[C/T]GTGGTGAAACCCCCG | 57626 |
rs536139358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945300 | CCATAACCAAACTTT[A/G]TTAATTAAAAATTTA | 57626 |
rs536156352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073634 | TTCTTCTAAAAACCC[A/G]GGTGTGGTGGTGTGC | 57626 |
rs536165710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066413 | AGTAAGACATGTAGA[A/G]TGCAAATAGAATAAA | 57626 |
rs536174350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69800694 | CACCTCATTCTATAA[C/T]TACTATTAATTTATC | 57626 |
rs536174733 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778986 | TGTATTTTTAGTAGA[G/T]ATAGGGTTTCACCCT | 57626 |
rs536183823 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69814194 | ACAGGCTTACCATAC[G/T]CAGAAAAATGAAACT | 57626 |
rs536186765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808089 | CTACTGAAGGCAACA[C/G]CACTGAAGCCCAGGA | 57626 |
rs536187040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010011 | TATGTATATCTATGG[A/C]AAGTGCATTACAAGA | 57626 |
rs536203003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880901 | TACCCACTGTCACAG[C/T]ATCTGTCATTAACTG | 57626 |
rs536204267 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70095017 | CTTATGTCTGAGCCT[A/G]GGTATCTCTCTTTTT | 57626 |
rs536226069 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69942037 | TTCAAAGGAGAGTTG[A/G]TGCCAATCTTACTGA | 57626 |
rs536226164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821391 | CTGATCTTGGCTCAC[C/T]ACAACCTCCACCTCC | 57626 |
rs536228802 | snp | C/T | 0.00079936 | 0.019976 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789877 | AAGGTTGAAGCAACA[C/T]TAAGTAAGTTTGGAG | 57626 |
rs536232025 | in-del | -/TATTA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69798627 | ATATTTTAATATATT[-/TATTA]TATTGGATATTGAAT | 57626 |
rs536238049 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028951 | CACTGCACTGCATTC[A/C]AGCTTGGATGACAGA | 57626 |
rs536245862 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70031792 | ACTGCAGGAAAGTTA[C/T]TAAACAAGGAAATGC | 57626 |
rs536267137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034343 | AACACAGAAATTCTC[C/T]TCCCTATTCCAAACT | 57626 |
rs536277298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796291 | TGTCCCCCCAAAACT[C/T]ATGTTGAAATTTGAT | 57626 |
rs536281954 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928095 | CCCCCATTGTTCCTA[A/C/T]AGATAGAATTTCAGA | 57626 |
rs536293015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913682 | CACTAGGAGGGAATG[A/G]ATTGCTTGTTCAATG | 57626 |
rs536299826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70040314 | AAGGGAGAAAGAAGA[A/G]AGGGAGTGGGGCAAG | 57626 |
rs536309857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100244 | TGTATGAGTCTTTCA[C/T]ATCTTTTCTCATTTT | 57626 |
rs536310744 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69748523 | TTATCTCCCCCTGGG[C/T]CCCTCCCATAACATG | 57626 |
rs536311690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093591 | AGAAAAATATATTTA[C/T]AGAAATATTTTGACA | 57626 |
rs536317353 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69728649 | TCTACTAAAAATGCC[-/A]AAAAAAAAAAAAGCA | 57626 |
rs536322146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886799 | AGACTTATGTCTTAC[C/T]ATCTTATACTCTGTG | 57626 |
rs536331352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760557 | ACAGGGTTTCATCAT[A/T]TTTCCCAGGCTGGTC | 57626 |
rs536335897 | in-del | -/GT | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729538 | ATCACGTCAGCAGAG[-/GT]GAGGAAAAAAACAAA | 57626 |
rs536342375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005809 | AAGCTGTTCCCATTA[A/C]ATCAATAAAGTATTG | 57626 |
rs536348805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094317 | ATGACAGAGTGAGAA[C/T]CCAACTCTCAGAAAC | 57626 |
rs536349360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086951 | GTTTGGTAAAGCAAT[A/G]TGGGTCAGGGGGGAA | 57626 |
rs536352361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945012 | TTTTTTTCAGATGGA[A/G]TCTCACTTTGTCGCC | 57626 |
rs536365026 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795785 | TATAGTTCTCTCTAG[A/T]TCCTGGTTACCCCAT | 57626 |
rs536367884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788808 | AAGATTTTAGAAAGA[C/T]TTGATCAGAGATCAG | 57626 |
rs536370342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919639 | TAGGAAGTTAAGGAT[A/G]GGGTTCTGAGATTTC | 57626 |
rs536371730 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725943 | TAGGTAGCTTTTCAT[C/T]ACATATGCAGGGTTA | 57626 |
rs536374539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004690 | GCAAACCATTTCTGC[A/G]TTAAAAATACTTTTT | 57626 |
rs536384347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69833032 | ATAATTCTTCTGAAC[A/G]TTGTCTTAGGCAAAG | 57626 |
rs536385438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847248 | GTAAAAGCCAGAAAA[C/T]ATTTACATTATAAAA | 57626 |
rs536400933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801940 | CATAGGTATACATGC[G/T]CCATGGTGGTTTGCT | 57626 |
rs536405898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951449 | GTAGAACCAGGTTAT[A/G]CTGAAGTTATCTGCA | 57626 |
rs536421284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017641 | GCAGAATGAGCCCAG[C/T]AGGTATGAGCAATAC | 57626 |
rs536423453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846535 | TCCCTTCAGTTACCT[A/G]TTTGAAAGCATTATT | 57626 |
rs536429782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024179 | AACCTTGAACCAAAC[A/C]AAATAGCTTATTTAG | 57626 |
rs536433464 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69728838 | AACATGAAGATTTGA[A/G]TGAATGAATGAATGA | 57626 |
rs536435334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL1, ATXN8OS | GRCh38.p7 | 13:70105235 | AAAAATAATAAACTA[C/T]TTTCAAAAGTAAGAA | 57626 |
rs536444700 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009018 | TCAATAAAAGTAAAG[A/G]TGAGATTATAACATT | 57626 |
rs536462607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036221 | TTAGAAACATTGCTG[C/T]TAGGGTTACTAGTTT | 57626 |
rs536466750 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69860358 | TGACTCAATTTCTAA[C/T]GGTAAGATTCTCAGA | 57626 |
rs536469281 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030133 | GACTTAGACTCCCAC[A/G]CAATAATAATGGGAG | 57626 |
rs536484292 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69936960 | ATCTTCCTGCAACTG[C/T]CCGTGGAGAATAATG | 57626 |
rs536486125 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908052 | ACTTTAATTAGAATA[C/T]ACTAAATATCAGTAG | 57626 |
rs536486305 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025447 | GTTAGTCTTGTTTTG[-/T]TTTTTTATGCACTTT | 57626 |
rs536487727 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060968 | CTATGTTAACAGAAA[A/T]ATGCCAGGCACACAA | 57626 |
rs536492788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726003 | TGTGTCTCCACTAGA[A/G]AGTCTTTTCTGATCC | 57626 |
rs536498586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915081 | TATAACACTGCTCAA[C/T]GAAATAAAAGAGGAT | 57626 |
rs536510530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703139 | GCTGTATTTTCATCC[C/T]TGAGGTTCAGGTCAT | 57626 |
rs536517234 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69853473 | TTCCTTTACAAATTA[C/G]CCAGTCTTGGGTATG | 57626 |
rs536524599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066934 | TATTCATAGAGTTGT[A/G]TTTTCTTTACGATTC | 57626 |
rs536531929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081389 | GCAATCAAGATTTTG[A/G]GTCCACTGCTTTTTC | 57626 |
rs536542174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828857 | GAAAGTAACTCCATT[A/G]GCCAGAGAACCACAC | 57626 |
rs536543643 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69938813 | TCTATATTTTCATTT[A/C]ATTTAGTAATCTGCT | 57626 |
rs536545362 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69808276 | AACATACCCTGAGGG[A/G]GGGTGCTTTTCTTCC | 57626 |
rs536552239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790386 | ATGTTGTGGTTGCCA[C/T]CAATCCACTACAAAA | 57626 |
rs536555383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725372 | GCAGGATGAAGGAAA[A/G]TTGGAAGAAGGAGCA | 57626 |
rs536559986 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69873754 | TATCCCAGAACTTAA[A/C/G]GTATATATATTTAAA | 57626 |
rs536572934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69702287 | GCTATATGCTTATTA[A/C]AAATTTTCCATCTTA | 57626 |
rs536577794 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69836114 | GAAATGAGCCTGACA[G/T]TCTTTGCCATTTTTG | 57626 |
rs536595013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69745994 | TAAGATTTTAACTTC[C/T]GGAGTAATGTTTGTT | 57626 |
rs536595257 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023003 | ATATGCATAACACAT[A/G]CATATCCTCTTAAAG | 57626 |
rs536596323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945100 | AAGTGATTCTCCTGC[C/T]TCAGCCTCCCAGGTA | 57626 |
rs536597583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029332 | GGTCACTGTAGAATA[C/T]AGTATTGCTAAGCAA | 57626 |
rs536602031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078719 | CAGTTATTTCAATAC[C/T]ATCACACTATTCAGT | 57626 |
rs536602447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872914 | AGGCCCCACCTCCAA[C/T]ACTGGGGATTAAATT | 57626 |
rs536607931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747492 | TAATATGTAAAACAC[A/T]TAGAACAGAATCGGA | 57626 |
rs536610989 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820472 | GTGTTTACTCTCTGT[C/T]TCCTAGTGATAAGCT | 57626 |
rs536618416 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788714 | ACTCATAGCCTAGGA[A/C]TCTTGATAGACAGTG | 57626 |
rs536632715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065428 | GACATATTAGGGAAA[A/G]CACAATAGAGTGGGG | 57626 |
rs536643736 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041543 | CAGGCTCCCTATTTT[A/T]GTTTCTACTAGGTCT | 57626 |
rs536645252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832901 | GGATAATTGGCAAGC[C/T]ACATGGCAAAAAACT | 57626 |
rs536645607 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963239 | GCATGGGTTCTAAAA[A/T]GTCTAATTTATGTTT | 57626 |
rs536646298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69871631 | ACTTCTTGAGCACTT[A/T]ACTGCTTAGAAATTT | 57626 |
rs536656259 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962415 | AAGTTATATTCTTTT[G/T]ACTTATTCCTGTTCA | 57626 |
rs536667776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834226 | CACACCTGTTTCCCA[C/T]AAACCTATTGAAATT | 57626 |
rs536676127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047846 | GTGTTAAAAGGTAGC[A/G]TGAAGAAACACTACA | 57626 |
rs536678860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912195 | TGGTCTTTACTCAAA[A/G]CTTCTGTTTGCCATG | 57626 |
rs536679527 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70027956 | GAAAATTTGAGAGGC[A/C]AAACATATTTAATGA | 57626 |
rs536679972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69921017 | CACCAACTTGGCAGA[C/T]AAAATGAAGAGCCTC | 57626 |
rs536689318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880262 | ATTAGAAATATATGT[A/T]ATATGCTTATAATGA | 57626 |
rs536689485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087417 | CAAGAGTAGTAAAAA[C/T]GGCATAGTCATGTGT | 57626 |
rs536691218 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69989678 | AGAGATCCTTCACTA[C/T]CCTGGTTAGCTGTAT | 57626 |
rs536699426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708519 | TAACATGAACACAAC[A/T]GGGTTTAGTGACATT | 57626 |
rs536710392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055117 | AAAGAAATTATCTCA[A/G]GACATTTATTAACCA | 57626 |
rs536712376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047125 | GTGGACTGACCACTG[C/T]AGAATACAGGAACAG | 57626 |
rs536722281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968263 | AAATAACTATGTACA[C/T]ATACATACATGATGA | 57626 |
rs536722794 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867982 | CGTTGTGCACATGTA[A/C]CCTAAAACTTAAAGC | 57626 |
rs536723799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997098 | TGGTGGCGCATGTCT[G/T]TAGTTCCAGCTACTC | 57626 |
rs536726947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753966 | TTCAGCCTCCCAGGT[A/G]GCTGGGACTAGAGGC | 57626 |
rs536738990 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70068800 | AACAAACATGCAGTT[G/T]GAAATTTAAGAACTT | 57626 |
rs536740686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70085438 | CTTGAAAAAGAAACA[C/T]GTAAGTCAAAGAAAA | 57626 |
rs536746366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918685 | TAACAAAAGGTCAGG[C/T]TGAACTTAGTTTCCA | 57626 |
rs536749013 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933197 | AATTATATATAACTA[C/G]TTACTAAGACCACGA | 57626 |
rs536750936 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70092166 | CAATTGAGCAGAGGA[C/T]ACAACTCCTTGCTCA | 57626 |
rs536760466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003417 | TTTCAATGACATGTT[A/T]AATACATTCAATTGA | 57626 |
rs536775027 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69749840 | AGAAATTATTATTTT[C/T]CTTTACACTTGTTAA | 57626 |
rs536778503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084935 | AGCAAATTCTTCAGG[C/T]ACTTTTTGGAAATAA | 57626 |
rs536783162 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839392 | TTATCATTTTACCAC[A/G]CAGAGTAAAAAAAAC | 57626 |
rs536785319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012142 | CGTAGAAATTAAAGA[C/T]GAGATTTGGGTGGGG | 57626 |
rs536787956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69751343 | ACCCTCACAGAACGC[A/G]TACAGGTGGATATGA | 57626 |
rs536788745 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758781 | TATTTAGCTTTTCCA[G/T]AGCATATAAAAATAA | 57626 |
rs536797859 | snp | C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760214 | TACTCTCTGCCTAGA[C/G]TCAGTATGGATAACT | 57626 |
rs536798199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814739 | CAAAAAAGGCTGGGC[A/G]TGGTAACTCATGCCT | 57626 |
rs536801328 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807746 | TGTGTGGAGAGTGCC[C/T]AGCAGCTGGCACTGG | 57626 |
rs536802602 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938225 | AACTGGTCAGTAATT[A/T]TTCTCTAAAATGGTT | 57626 |
rs536815170 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946073 | GCTGAGTGAAAGAAA[A/C]CAGACAGAAAATAAA | 57626 |
rs536826812 | in-del | -/AG | 0.153997 | 0.230832 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855397 | GATAGAGATAGAGAT[-/AG]AGATAGAGATACAGA | 57626 |
rs536828479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69892707 | CATAAATGATACTTC[A/G]GGAAAGCCTGTTATA | 57626 |
rs536831591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898817 | CTATTCAATGCCACA[C/T]GTAGCTTGTGCACAA | 57626 |
rs536845778 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69786879 | CAGACAAACAGAGCC[A/G]AATCATGAGGGAACT | 57626 |
rs536847989 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69983091 | AAAAGAAATCAATAA[A/G]GCAATCCCATTTATA | 57626 |
rs536872175 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69914311 | TTTACTCAACAATAA[A/C]ATTTCTAAATTATGG | 57626 |
rs536874578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951103 | CTCTTTGTCTTGTTG[A/T]CTGAGAAGAAAAACT | 57626 |
rs536876185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740847 | AAAACAAAATTGGGA[A/G]CCAAAAATAGTATTA | 57626 |
rs536891497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69898240 | ATTCCTTCCTGCCCT[C/T]CCAGTAAGCCTAAGG | 57626 |
rs536893544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985111 | AGCGAGACTCTGTCT[A/C]AAAACAGACAAACAA | 57626 |
rs536894472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068057 | AAGTAAAAAAAAAAA[A/C]AGGGCCAGATGCAGT | 57626 |
rs536895318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69905821 | AAAGTTTATGCTCAG[A/G]ATCACACGACATACT | 57626 |
rs536895445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979509 | TACTAATTTAAAAAG[A/G]AGACTTTAACATTTT | 57626 |
rs536895907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075050 | CTGACAAAAGTCAGA[C/T]TAATAGGAAGAAAAG | 57626 |
rs536898588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69778531 | ATTATCAAGACAGAT[A/G]AGACATAGTTCTTGA | 57626 |
rs536907220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69984582 | ATCAGATACTGCCTC[C/T]TCTAGCTAGTCTGTA | 57626 |
rs536907680 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69766198 | TAAGATTTTAAATTT[A/C]GCTTGGAGGACACAC | 57626 |
rs536908671 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035629 | TAAAACAACCATGTC[A/C]CTCTAAAACAGATGA | 57626 |
rs536908931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779792 | CCTATGCAAAATTTA[A/T]TTTTTATTTATTTTA | 57626 |
rs536912523 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841330 | ACCAAAAGACTCAAC[A/C]AAAAAAACAGTAGGT | 57626 |
rs536915710 | in-del | -/AAG | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719067 | TTTTAAAAGTATATC[-/AAG]AAGAAATTTAAAGAT | 57626 |
rs536919204 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70046220 | GAGCATAAGTGTGAG[-/A]AAAAAAAAAATGTCA | 57626 |
rs536929203 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69887364 | CAGGTAAACCTTGAC[C/T]ACTGCTTTGGTGTTC | 57626 |
rs536934011 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074509 | TCGTCCACCCAAGAG[A/T]TTCCAAGAGGGCATT | 57626 |
rs536960687 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | KLHL1 | GRCh38.p7 | 13:69770308 | TGCAGCCTGCTGGCC[A/C/T]GAGTGGGCAGAGTGA | 57626 |
rs536963713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69777959 | AAATGTTCCTCATTT[C/T]TAACTTGACTACTTC | 57626 |
rs536974736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080961 | GCAGCTTAAATTCCT[C/T]TAAATCCAGCTTGAT | 57626 |
rs536977553 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700489 | TGGAGATACATACTT[C/T]TTTAAATTTGAAAAT | 57626 |
rs536983930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028551 | TCTGCCTGGTCATAA[G/T]GAATGAATATTTCCC | 57626 |
rs537000344 | in-del | -/TT | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091312 | CCCTTCCTCCAACTC[-/TT]TTTTCTCTTTCAACT | 57626 |
rs537001068 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962684 | ATGATATTTTAGAAT[-/G]AAAAAAATTATGATA | 57626 |
rs537002107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004800 | AAATAAATCAAAATT[A/G]CTGTACTAATTAAAA | 57626 |
rs537002134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69886556 | TATATGAAAATTAGC[C/T]GAAACCTAATGGTAA | 57626 |
rs537003023 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70104882 | TTTTACTTTGGAAAT[A/G]CTGTCTTTTCTGGGC | 57626 |
rs537003302 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70083642 | AAAAAGTAAAAACTT[C/T]AATCAAAGAAAATAA | 57626 |
rs537005593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737875 | CACAGCACACCTGCC[C/G]CACCAAGCTGCAGTC | 57626 |
rs537012390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827226 | AATGGAAATATAATA[C/G]AGCATATTTAATTTT | 57626 |
rs537016185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926992 | AATTCACACTTCCCA[A/G]TTTCAAAATTTTCAC | 57626 |
rs537025572 | snp | C/G | | | intron-variant, utr-variant-5-prime | KLHL1 | GRCh38.p7 | 13:69970754 | GAGATAAAGAGGAAG[C/G]AAGTCTTCATTCTTG | 57626 |
rs537028597 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70014615 | TATTATCATCCATGC[A/G]TGTATAATGAAAATC | 57626 |
rs537056944 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69802390 | TATACCCAAGAACTC[C/T]CACTATTGAGTGAGA | 57626 |
rs537058456 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69824717 | ACGTAGGTTGAAAAA[A/T]TATTCAAAGGAATAG | 57626 |
rs537063104 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70102317 | ATTATTTCTTTCCAT[C/T]TCTAGGTTATATTTG | 57626 |
rs537067578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039621 | GTTAATACTGCCTGC[C/T]TTTGGATTCCTTGAA | 57626 |
rs537071559 | in-del | -/A | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69703494 | AATTTATTATTAAAG[-/A]AAGAAAAATATTTTA | 57626 |
rs537079908 | snp | A/G | 0.138207 | 0.223612 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919552 | TTGGGTACATTAATG[A/G]CACCAATTTTCTCTC | 57626 |
rs537086710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69788494 | GGAAGGGGAACATCA[C/T]ACTTCGGGGACTGTT | 57626 |
rs537091720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714264 | TATTTTATTACATCA[A/G]TTTTTCAAGGTTGAG | 57626 |
rs537092083 | in-del | -/G/GGG | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:69708242 | AGCCTAAATTTGCTA[-/G/GGG]GGAAAAAAAAGGAAA | 57626 |
rs537097402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720302 | CAGTTTAATCCTAAT[A/G]AAATAGTCCTTCCCC | 57626 |
rs537105875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038853 | GCCTTGGCCTCCCAT[A/T]GTGCTGGGATTACAG | 57626 |
rs537109645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099113 | ATGGAATTTTACTTA[C/T]ACTATTCTCTCTGAT | 57626 |
rs537111135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045738 | AGGACATTCCTGTAA[C/T]ACTTGTCTCTTTACT | 57626 |
rs537118483 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893395 | GCCCGCCACCGCGCC[G/T]GGCTAATTTTTTGTA | 57626 |
rs537127716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69752244 | ATCACTGTAGAGATA[C/T]GAGAAGAGACTATTG | 57626 |
rs537134664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69832505 | ATGGGTAGAATCATT[A/G]GGAAAATAATCATAC | 57626 |
rs537141154 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011383 | TTAGTATTTTAATAC[A/T]ATATACCTGGACCAG | 57626 |
rs537142875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925836 | AATATGAGATAAATA[A/G]TTTAGCTTGTATACT | 57626 |
rs537157103 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010521 | TGTAAATCTTGTGAG[G/T]CCTCCCCAGCCACAT | 57626 |
rs537158211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725899 | TTTCTAGCCCTATGT[A/C]GCATGGTGCATTCAT | 57626 |
rs537164219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69808313 | GTTGCTTCTGTTCCC[A/G]CCACTACCTACTGTC | 57626 |
rs537174506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69773027 | GCATTTGATGTTTTG[C/T]AGACCATTACACAGG | 57626 |
rs537176897 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69783801 | TCTAGCAAGGCAGGC[A/C]AACATTCAGATTCAG | 57626 |
rs537178832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838129 | TTCCCTGCAGCTACA[A/G]TTTTGAAATCTCAGT | 57626 |
rs537192592 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837687 | ATATATATATATATA[C/T]ACACATATATATATA | 57626 |
rs537200777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073915 | ACCGCAGCCTCCACC[C/T]CCTGGGTTCAAGCGA | 57626 |
rs537201866 | in-del | -/GATA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70089611 | TAAATTTTATAGATG[-/GATA]GATATTTAAGTGTAT | 57626 |
rs537207257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740156 | ATTTATTCAAAAGTG[A/C]TATAAATATTCCCAT | 57626 |
rs537210003 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69912406 | GAAAAAAATTGTATT[G/T]TATGTGATGGCTTTC | 57626 |
rs537212383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022974 | TTTATGTTGAAGTTT[C/T]GATCATGTCTTCCAT | 57626 |
rs537212603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822049 | CCAAAAATTAAAAAT[A/T]TTAGCTGGGTGTAGT | 57626 |
rs537224977 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725233 | TGTTATGAAAAACAG[G/T]CACCAGTAATTATTG | 57626 |
rs537230656 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70008405 | ATAAGTTTTTGTCAT[C/T]CTATGAACATATAAG | 57626 |
rs537234844 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69921922 | TGTTGAATGATTGAT[-/T]TTTTTTTTTTTTTTT | 57626 |
rs537237484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979960 | AAATACTCCTTAATC[G/T]ATTGCAATTCGACTT | 57626 |
rs537237764 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70044228 | TACATTTGCTCCCAC[A/G]TACATGCACTTCACT | 57626 |
rs537241142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772574 | TGTTTTCTAAATCTA[A/C]TCTAGTTTGTCCACA | 57626 |
rs537242076 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | KLHL1 | GRCh38.p7 | 13:69702076 | TGGAGTTTGCATGGA[A/C]ACATTTGTGATAATA | 57626 |
rs537246165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69784440 | GTATTCAGGAAACCC[A/G]TCTCATGTGCAGAGA | 57626 |
rs537247710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69764392 | AATCTATTCTGGTTC[A/G]AAGGGAGGCCCAATT | 57626 |
rs537253525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028933 | AGTGAGCTGTGATTG[C/T]GCCACTGCACTGCAT | 57626 |
rs537264167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69747325 | TGATTGTCATTGTTT[A/T]GGTTTTTGTTTATAT | 57626 |
rs537272151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035091 | TTATTATATTAATAA[C/T]CCTTGAAGGAGGATC | 57626 |
rs537273766 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70021708 | TCCTAATAGGTGCCT[C/T]AAGTGAAGCCCCAAA | 57626 |
rs537280598 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69845604 | TCATGTGTATTGTTT[A/C]TATATACCTGACAAA | 57626 |
rs537287895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69869266 | TTATCATATGGAAAG[C/T]AAATAAAATTTCTTC | 57626 |
rs537291178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814279 | AAATGTAAGACCTCA[A/G]ACCATAAAAATCATA | 57626 |
rs537294553 | in-del | -/AT | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019906 | GCTCCATCCTCATGA[-/AT]AATTAATCCTTTCAT | 57626 |
rs537295244 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69769626 | AATGCTGCCTTTTCC[A/C]AGGCTACCTGCAGCC | 57626 |
rs537304924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709109 | ATGAGGCGCTGGTCG[A/G]ATGCTAGAAAACCAG | 57626 |
rs537307914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69904812 | ATGCTGCTGAACTAT[A/G]CTGAGTTTTTAAATC | 57626 |
rs537308355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789846 | GATTTTGTTTTGTAT[A/T]TGTTTTGCATTGTCA | 57626 |
rs537312080 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69741834 | TCCTTTGAAATTTAG[A/T]CATTAAGATATTCTA | 57626 |
rs537324631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69858323 | GATAGACCTAATAAG[A/G]ACTTTGAACTTCCAG | 57626 |
rs537332625 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL1 | GRCh38.p7 | 13:69820844 | GATTTGGGTCAAACA[A/C]ATGTGACGTTTGGCA | 57626 |
rs537335205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834163 | CAGGTGATGGGTGCA[C/T]CAAAATCTCAGAAAT | 57626 |
rs537336098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827836 | TTTTGGAATTACACA[A/C]AATCCTGATTAAAAC | 57626 |
rs537340532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731266 | AGAGGAGTGAGAAGC[A/G]GAAGGTAACTACTTC | 57626 |
rs537340533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738379 | TCCAGCAAGTGCACA[C/G]AACTGGGCGGAGGCT | 57626 |
rs537342256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920916 | AAAAAATACATAAGC[A/C]GTCATAAATGCTAAC | 57626 |
rs537348310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69796149 | AATATGTATCTCAAC[A/G]GTTTAAAATTAAGAC | 57626 |
rs537356129 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920390 | GTGCTATTTTAAGAA[A/C]TATTTAGGCAGTACC | 57626 |
rs537361942 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880085 | TGGCACTCATATTGT[A/G]GAAATATCTCTGTGT | 57626 |
rs537364926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012527 | CAGTCTTTGAAGAGG[A/G]GGAGGGGGACTTGAA | 57626 |
rs537370530 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070984 | ATAAAGGGAAGGCAC[-/A]AAAAATCGGAAGACA | 57626 |
rs537371690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69912854 | GCTGGGAGACTACCT[C/G]CTTGCCTTCTGTGAT | 57626 |
rs537378471 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839830 | AGGTTATTGTCTCTG[A/C]AAATTATTTTGTGTA | 57626 |
rs537385438 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755635 | ATATTTGAATTCATC[A/T]CCAAAGTAATTTTAA | 57626 |
rs537388510 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69843511 | CTTTAACTAATTAGG[G/T]TGGATTAATTTTAGC | 57626 |
rs537405895 | snp | C/G | 1.70499e-05 | 0.0029197 | missense | KLHL1 | GRCh38.p7 | 13:69940052 | TACCATTGTGTAGCT[C/G]TGGGCCACCTTCATT | 57626 |
rs537407668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69879438 | TTCTCTTGGTAGCAA[C/G]ACACACAAACATCTC | 57626 |
rs537439564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968166 | CATCAACAGCGAGTT[A/G]AGACCCATCACTAGC | 57626 |
rs537441378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795634 | TCATAGTCATTTTAA[G/T]TATTATATTTTTGTC | 57626 |
rs537450130 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69941278 | AGTGGAATAAAACTC[A/G]AAATTAATTCCAAAA | 57626 |
rs537451293 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69789251 | ATTTTTTTAAAATTA[-/C]TTTTTTAAATTATTT | 57626 |
rs537451598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099631 | GGATAATAAATACAA[C/T]AGATAAGTTTATGTG | 57626 |
rs537463153 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69887129 | ATTTTAAAATTTCTA[A/G]TTCCTTAAGCGTCCT | 57626 |
rs537473135 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70059401 | TCTCAAACTCCTGAC[A/C]TCAAGTGATCCACCT | 57626 |
rs537501886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907550 | CTTCGCTAGATATTG[A/G]AAGTCATGGGTAGAG | 57626 |
rs537507092 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70024302 | ATTCAAAGAAACCTA[A/G]TAGTTTATATTTTCA | 57626 |
rs537507624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060893 | AATAGAGTACCCTTC[A/G]GCTATAAAAAAAGAA | 57626 |
rs537524870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974295 | ATATGTTCAGAATAA[C/T]ACATATAAAGGTAAT | 57626 |
rs537526437 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908123 | AACTCAGGACTGAGA[A/T]TGTAGCTTGTGGTGT | 57626 |
rs537527571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69822802 | TATAGAATAACTGGT[G/T]TAATATAATTATCTG | 57626 |
rs537563795 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69719841 | TAGAAACTTGGATAG[A/G]TTTAAATTGCATACT | 57626 |
rs537567381 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760379 | TATTATTTTGAGACG[A/G]AATTTCACTCGTTTT | 57626 |
rs537590955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845904 | TTGAAAAAAAATAGA[A/T]CTTAAAAAGTCAATA | 57626 |
rs537596769 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080887 | ACGTGAGCCACCACG[C/T]CTGGCTCTTCTACCA | 57626 |
rs537597939 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938795 | TATCTTCTTCCTTTT[A/G/T]TTTCTATATTTTCAT | 57626 |
rs537609862 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054901 | AAGAAAAAAATAATG[-/A]AAAAAAGGAAATACA | 57626 |
rs537633138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866799 | GGGCAATTCACTGAC[C/T]ACATTTCAGACACAA | 57626 |
rs537660056 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69705057 | CTTTAGAGACAGGTT[A/G]ATAAATGACACATTG | 57626 |
rs537673417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69956443 | ACCTAAAGGGAACCA[A/G]CATTAGATGGGGAGA | 57626 |
rs537674423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69841756 | AGCCCAAATGTCAAA[G/T]CAATCCTGATCAAAA | 57626 |
rs537679458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095339 | TTAGATCCTTAGGAC[C/T]ATCAGGAATTGACTA | 57626 |
rs537682036 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065093 | ACTTGATACTCTAAC[A/C]CTGTTTATTTCAAGA | 57626 |
rs537682900 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69966389 | AGCCTGGACGACAGC[A/T]CATCGTTTGCAGAAT | 57626 |
rs537685444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70041099 | CTCTTTGGTTCTTCA[C/T]TGTCTCTTCTATACC | 57626 |
rs537687373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69888390 | GGGTCATTGCAGATA[C/T]AGTTGATTAAGTTAA | 57626 |
rs537698722 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69984881 | TGGGAGGCCAAGGTG[A/G]GCGGATCGCATGATG | 57626 |
rs537711450 | in-del | -/AAAA | 0.491473 | 0.0647364 | intron-variant | KLHL1 | GRCh38.p7 | 13:69757958 | GCGAAACTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA | 57626 |
rs537716584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69761383 | TAATACAAAAATAGG[C/T]TACAGCCTGTTTACA | 57626 |
rs537716946 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100064 | AGAATAAACTCATCA[A/G]TTTGTAACAAAAAAG | 57626 |
rs537729903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080443 | TCTACCAGATAAACC[C/T]AGAGGCTCTATTTCC | 57626 |
rs537735411 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69777835 | TTCCTACTCATGTGT[A/G]AAGTCCTTGAATACA | 57626 |
rs537742881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927921 | TATTATGTTCACACA[A/G]TAACTTGTATATGAA | 57626 |
rs537745297 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69946310 | ATACATTTTGTATAT[A/G]TGCAGTTTATTATAT | 57626 |
rs537749187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055224 | CATCCGGCAGCTGAC[C/T]TATCAGTGAGAACCT | 57626 |
rs537755049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062011 | AAGTTAGCCATATTC[A/G]CCCTGCAGTGCTGAA | 57626 |
rs537756596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69872422 | GATCCCAGCAACTTA[C/T]AGATGCACTGGAGTA | 57626 |
rs537761867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968404 | TATATTTTGGTGACT[C/T]GCTTAATTGCGATAG | 57626 |
rs537766191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005605 | TTAGATATATGTTAA[C/T]GTATCTAGTATTAAT | 57626 |
rs537779421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768168 | TATCCATAGATCAAG[C/T]TTTCTTTAGCTTACC | 57626 |
rs537782941 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753827 | TCATTTTCCATAATG[A/G]CATAGAAATAATTGA | 57626 |
rs537790818 | in-del | -/AATC | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099892 | TATTTATTCATTCTT[-/AATC]TATTTATGTATTCTT | 57626 |
rs537792350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940731 | TTAAAATTGTCTATA[A/C]TTTTGGTTTTTAGTT | 57626 |
rs537796929 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69751508 | TGTGGGGATGAGGAA[C/T]TCTTGGCAGAAGAAA | 57626 |
rs537805069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929740 | TATTAGTCATATTTT[C/T]GGGTTAAAACAGCAA | 57626 |
rs537808058 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951996 | CATAGATTATGTGAC[G/T]GTTATTTCCCCTCTT | 57626 |
rs537817303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69721187 | ATATCTGAGTGCCTC[C/T]TTTGGAAAGGCTAGT | 57626 |
rs537825182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69894884 | TCACCCTAACTAGCA[C/T]CTCTATCATGGCATG | 57626 |
rs537830947 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69774588 | TCTAAATGATTAAAT[C/G]ACAAGTGTGGCTCTG | 57626 |
rs537835427 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975878 | ATTATCTAGAATAAC[A/G]TACAGGTTTTTATCA | 57626 |
rs537840477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69868665 | GTGAGTATCATGATG[A/G]TAGCTTATATTTCAA | 57626 |
rs537849958 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024118 | GGCACATTCAGGATG[C/G]TATGGCGTAGACGAT | 57626 |
rs537857892 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767479 | AGGTGGGAGAATGGC[A/T]TGAGGCCAGGAGTTT | 57626 |
rs537865350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70036932 | TTAATGTTTGTAATT[A/T]TGTTAACAAATTATA | 57626 |
rs537871754 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70079841 | TTGAACTCAGCATAC[C/T]GAGCTTTAAGTCCAT | 57626 |
rs537873201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741644 | TCTTGATCAAACTTC[A/C]GACAGTTTTGTCCTG | 57626 |
rs537879007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867991 | CATGTACCCTAAAAC[A/T]TAAAGCATAATAAAA | 57626 |
rs537894037 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69994570 | TACAAGATATATCAC[A/C/G]CATCAAATAAATTAC | 57626 |