SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6968 | snp | C/T | 0.0228194 | 0.10435 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039012 | ATGACCATTGAGGAC[C/T]TGAATGAAGCTTTCC | 23510 |
rs9660 | snp | A/G | 0.341409 | 0.232689 | utr-variant-5-prime, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042651 | TTTTCAGGATCCCAA[A/G]ATGGCTGGGCGAAAA | 23510 |
rs1127088 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064397 | TGGGGACTTCTCCTT[C/T]TATGAAAGCCTCCTC | 23510 |
rs1466681 | snp | A/C | 0.362104 | 0.223456 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044960 | GATTTTAAAGTTACC[A/C]GGGAACCAAGCACCC | 23510 |
rs1491765 | snp | A/G | 0.357877 | 0.225527 | intron-variant | KCTD2 | GRCh38.p7 | 17:75032828 | TGGCCCTGGGGCAGA[A/G]TGCTGGATCCCAGCA | 23510 |
rs1802462 | snp | A/C | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038949 | TATTGGCCTCACCAA[A/C]CAATTGAGAATTTAT | 23510 |
rs1802463 | snp | C/T | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038997 | TTGAATGAAGCTTTC[C/T]CAGAAACCAAATTAG | 23510 |
rs1802465 | snp | C/G | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038959 | AAAGTATCCCTATTG[C/G]CCTCACCAACCAATT | 23510 |
rs2291535 | snp | A/G | 0.320096 | 0.239972 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039408 | CCTGTCAGAGTGAGC[A/G]CCCCCACTCAGGGTA | 23510 |
rs2307008 | snp | A/G | 0.464416 | 0.128553 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046587 | GAGCGTCCCTCGGCA[A/G]GTTAACACTGTCTGC | 23510 |
rs2307009 | snp | A/C | 0.0715223 | 0.175059 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046672 | GGACTGCACGAGACA[A/C]GGCTTGTGGCAGCGC | 23510 |
rs4076115 | snp | A/G | 0.131723 | 0.220251 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063741 | CTTTCTCCAGCAGCC[A/G]GGACCCTCTGGAGAG | 23510 |
rs4365317 | snp | C/G | 0.496968 | 0.0388195 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063725 | TGCAGCTTTGCCTCA[C/G]CTTTCTCCAGCAGCC | 23510 |
rs4435292 | snp | A/G | 0.366266 | 0.221319 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039698 | TGTTAGAAACAAGGA[A/G]TTGGAATTAGAAAAA | 23510 |
rs4447462 | snp | A/G | 0.357451 | 0.225731 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051388 | ctcccgggttcaagc[A/G]attttcctgcctcag | 23510 |
rs4788858 | snp | A/C | 0 | 0 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043238 | aaagaaaaggaaaGG[A/C]CAGTGTAGCTTTTCA | 23510 |
rs4789126 | snp | C/G | 0.378568 | 0.214407 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032295 | CATTTAGTCTTTCCC[C/G]TACAGAGGCTGTGGC | 23510 |
rs4789127 | snp | A/G | 0.378174 | 0.214642 | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75032657 | GCTGGGAGTGAGGTT[A/G]GAGCTGTAAGATCCA | 23510 |
rs6146149 | in-del | -/CACACACACAC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062744 | ACACACACACACACA[-/CACACACACAC]GCTTCTAAATCGTGG | 23510 |
rs7210163 | snp | A/G | 0.116138 | 0.211142 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035095 | AATTGGCCTCTCTAG[A/G]AGGTAGCTGCAGCCG | 23510 |
rs7210415 | snp | C/G | 0.420574 | 0.182769 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041773 | tgcctggctgaggca[C/G]gtggattgcttgagc | 23510 |
rs7211204 | snp | A/G | 0.49655 | 0.04139 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050332 | actggcacaatcttg[A/G]ctcactgcaacctca | 23510 |
rs7211939 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052336 | tcatgcctgtaatcc[A/C]aacacttggaaggcc | 23510 |
rs7217434 | snp | A/G | 0.213333 | 0.247296 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044589 | tcaggtgatccaccc[A/G]cctcagccttgcaaa | 23510 |
rs7218004 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | KCTD2 | GRCh38.p7 | 17:75032748 | GAGCCCCGGGCGGGC[A/G]GGTTGGGGGAACATG | 23510 |
rs7218157 | snp | A/C | 0.489492 | 0.0717183 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030949 | AACAATACAAAAATA[A/C]AATTAGCCAGGCGTG | 23510 |
rs7218282 | snp | A/G | 0.0592355 | 0.161582 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030687 | TGTATAAATTTCTTA[A/G]ACTGTTCTATATGAT | 23510 |
rs7219493 | snp | C/T | 0.464629 | 0.128197 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048093 | ATATCACACTGCTTT[C/T]CTATAGTCCTGGTCG | 23510 |
rs7223981 | snp | A/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031750 | ccccacctataaact[A/T]ggggggtttttttgt | 23510 |
rs7224300 | snp | A/G | 0.278133 | 0.248412 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033161 | TTCAAATGAGACTGC[A/G]TCTCGCTATGTTGCC | 23510 |
rs7503086 | snp | A/C | 0 | 0 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039894 | gaatcatatgctata[A/C]tcttctttttcttgt | 23510 |
rs8064912 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037361 | aaaaaaaaaaaaaaa[A/G]aaagaaaTGGCAGAA | 23510 |
rs8065776 | snp | A/G | 0.421209 | 0.182174 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055815 | ccagcctgggcaaca[A/G]gagcgaaactcccat | 23510 |
rs8073270 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035852 | aaacaaacaaacaaa[C/T]aaacaaaAAACTCCA | 23510 |
rs8077242 | snp | C/G | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036757 | TCAGATCCTCAGCGG[C/G]ATGGCTGAGTGCCAG | 23510 |
rs8077664 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037017 | GATTTCTCGAGGGTT[A/G]TCAGGCATTGTTGCT | 23510 |
rs8078243 | snp | A/C | 0.140242 | 0.224618 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036706 | CTGCATTTTTTCTCA[A/C]ATCCCTGCGCTTTCA | 23510 |
rs8079265 | snp | A/G | 0.209693 | 0.246729 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037067 | CTGCAAAAATGGGCC[A/G]GGTGCGGTGGCTCAC | 23510 |
rs8079749 | snp | C/G | 0.0283406 | 0.115616 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031727 | ctaacctctctgaac[C/G]ttagtttccccacct | 23510 |
rs8080887 | snp | A/G | 0.162581 | 0.234218 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040504 | AGCACCTTGAATTGT[A/G]AAGAAATTCTGATTT | 23510 |
rs9891685 | snp | A/G | 0.292008 | 0.246445 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037283 | CGGGAGGCAAAGGTT[A/G]CAATGAGCAGAAATC | 23510 |
rs9900856 | snp | A/G | 0.464841 | 0.127841 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037832 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 23510 |
rs9904728 | snp | C/T | 0.320096 | 0.239972 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034540 | GTGCTCCTTGATAGG[C/T]GTTCAACCATAGTGC | 23510 |
rs9905052 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035189 | CCTTCGTGGTCGGAA[C/T]GTTTTAATCCCTGCA | 23510 |
rs9906330 | snp | A/G | 0.401924 | 0.198543 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053342 | TGCTTACCAGATGGC[A/G]GGAGGAGGCGCCCAG | 23510 |
rs9911825 | snp | C/T | 0.166832 | 0.235761 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057369 | TGGCATCTTAAATAC[C/T]TGGGACTTTGACAGC | 23510 |
rs9915277 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031231 | GGCTCATATGCAGGA[C/T]GTACAAAATTTCCTA | 23510 |
rs9915968 | snp | C/G | 0.496937 | 0.0390173 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063521 | TGCACCCTCCAAGAC[C/G]TGCAGCAGATGCAAA | 23510 |
rs10512598 | snp | C/T | 0.320575 | 0.239832 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042037 | CAAAGGCCTTGTGGT[C/T]GATTGAACTGTAAAT | 23510 |
rs10533801 | in-del | -/AC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062700 | CCCCCCTCACCCCCA[-/AC]ACACACACACACACA | 23510 |
rs11077772 | snp | C/T | 0.37778 | 0.214877 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039603 | TAGCCAGACTTCTCT[C/T]TGGTGGAGCCACTGA | 23510 |
rs11077773 | snp | C/T | 0.470908 | 0.117046 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063978 | TTGCCAAATGTGTTA[C/T]GTTGTGTCTCAGAGA | 23510 |
rs11312083 | in-del | -/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044034 | GCACACGTTGTGCAC[-/T]TTTTTTTTTTTTTTT | 23510 |
rs11538852 | snp | G/T | 0.130351 | 0.219509 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065663 | TGTTTCTGCACAGTT[G/T]TAACTGCTCTTGGGG | 23510 |
rs11538853 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064699 | TTTTACAGCTGTAAA[G/T]TGTTAGATGAACTGC | 23510 |
rs11538854 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063366 | TCTGGGGGATGAGGG[C/T]GGAAGGCCTAGCTCC | 23510 |
rs11651848 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052618 | atcccagctacttgg[A/G]aggctgaggcagcag | 23510 |
rs11867756 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033130 | TTTAATAATTTTTTT[C/T]CTtttttttcttttt | 23510 |
rs11869630 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033131 | ttaataatttttttt[C/T]Ttttttttctttttt | 23510 |
rs11870474 | snp | A/C | 0.164873 | 0.23506 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034715 | GCGGTGCCCTGTAAC[A/C]CCGAGAAGAAGTGCT | 23510 |
rs11871228 | snp | A/G | 0.409552 | 0.192466 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051547 | CCTTGGCCTCCCGAA[A/G]TGCTGCGATTACAGG | 23510 |
rs12103574 | snp | A/G | 0.166832 | 0.235761 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056554 | AGATTCTGAAGGCTT[A/G]TGGATTTATACCCCT | 23510 |
rs12150430 | snp | A/G | 0.362941 | 0.223034 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058824 | ataaataggccgggc[A/G]cggtggctcatgcct | 23510 |
rs12232542 | snp | C/T | 0.31357 | 0.241783 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060662 | CGGCCAGGGAGGGCG[C/T]GCGTGCGAGGGCGGG | 23510 |
rs12600475 | snp | A/C | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049654 | GTGAGTGTCTGTAGT[A/C]TGAAGAAGCAAGACA | 23510 |
rs12602540 | snp | A/G | 0.32955 | 0.237006 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064016 | TTCTGTGACTCTCTT[A/G]GAAATGCCTTGACTG | 23510 |
rs12602633 | snp | C/G | 0.336702 | 0.234484 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064590 | TCCCTAGGACCCTCA[C/G]TCTCCTTGTTTCTCT | 23510 |
rs12936866 | snp | A/G | 0.397994 | 0.201489 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055955 | AGAATCGCTTGAACT[A/G]AGATAGCAGAGGTTG | 23510 |
rs12938569 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060070 | TGGGAAGTGTGGTGC[A/G]GCCGTTTCCCCTACT | 23510 |
rs12938889 | snp | A/C | 0.362313 | 0.223351 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043834 | ATTTACTTATGTGTA[A/C]AATGGGCATTATCAG | 23510 |
rs12939787 | snp | C/G | 0.132409 | 0.220618 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044071 | actctgtcccccggg[C/G]tggagtgcagtggca | 23510 |
rs12940199 | snp | C/T | 0.399073 | 0.200692 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058664 | attagccaggcttag[C/T]ggcaggcgcctgtaa | 23510 |
rs12940952 | snp | A/G | 0.170733 | 0.237101 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051346 | ctggagtgcaatggc[A/G]ctatcacagctcact | 23510 |
rs12943148 | snp | C/G | 0.40157 | 0.198813 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055637 | tcaggagttcaagac[C/G]agcctgactaacatg | 23510 |
rs12943281 | snp | A/G | 0.160609 | 0.233472 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033999 | GAAAGTTCCTTTTAC[A/G]GAATTTTTTATTTCT | 23510 |
rs12946754 | snp | C/T | 0.131038 | 0.219882 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049571 | CGCTTTGCAGATAAC[C/T]TCAGGAGTTCTTTCC | 23510 |
rs12949127 | snp | A/T | 0.166832 | 0.235761 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058977 | gtggcgggtgcctgt[A/T]gtcccagctacttgg | 23510 |
rs12949352 | snp | A/G | 0.123105 | 0.215401 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054143 | ctacctcagcctacc[A/G]agtagctgggactac | 23510 |
rs12949451 | snp | A/C | 0.251578 | 0.249995 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036224 | gggcccggccaggga[A/C]tggagttttgtctgc | 23510 |
rs12950279 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047229 | TGCGCGCGggcagca[A/G]cggtggcggcggcgg | 23510 |
rs12950646 | snp | C/G | 0.494315 | 0.0530107 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045375 | aggagacagggtttt[C/G]agatcaaccggtctg | 23510 |
rs12951145 | snp | A/G | 0.213635 | 0.247341 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037981 | ATGAACCCATGAGGT[A/G]AAGGTTGCAGTGAGC | 23510 |
rs12952376 | snp | C/T | 0.49724 | 0.037049 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047242 | cagcggtggcggcgg[C/T]ggtccaagatggcgg | 23510 |
rs16967530 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030674 | GATTGCTCTGGCATG[C/T]ATAAATTTCTTAAAC | 23510 |
rs28412160 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044495 | TAGGCGTGAGCCACC[A/G]CGCCCGGCCCTAATT | 23510 |
rs28438465 | snp | A/G | 0.0865458 | 0.189163 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038720 | GCCTCAGTAAGTGGC[A/G]CCTACACAGCCCGTC | 23510 |
rs28497354 | snp | A/G | 0.19646 | 0.2442 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033169 | AGACTGCATCTCGCT[A/G]TGTTGCCCAGGCTGG | 23510 |
rs28501229 | snp | C/T | 0.20111 | 0.245173 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041905 | TAAGAAGGGGTGAAC[C/T]GGCCCAGGTCAGAAA | 23510 |
rs28576234 | snp | C/T | 0.351853 | 0.228311 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044480 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 23510 |
rs28587464 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044634 | GGCATGAGCCACCGC[A/G]CCCGGCCTGCATTTT | 23510 |
rs28648787 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041371 | AAAAAAAAAAAAAAA[A/G]AAGAGCAGAGAGGTG | 23510 |
rs28694537 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057860 | GTCACTGCACCCGGC[A/G]ATCGTTATACCTCTT | 23510 |
rs28797168 | snp | A/G | 0.084728 | 0.187577 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058516 | CTCAAAAATAATAAT[A/G]AGGCTGGGTGCGGTG | 23510 |
rs34037833 | in-del | -/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032496 | GGGTAGTGTGGGAGT[-/G]GGGGGTGTGACATGG | 23510 |
rs34316730 | in-del | -/A | 0.397994 | 0.201489 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058338 | AAAAGGAAAAAAAAA[-/A]TAAAAAATTAGCTGG | 23510 |
rs34415927 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031542 | GGGAGAACTGGCAGG[A/G]TAACAGCATGTCACT | 23510 |
rs34551845 | in-del | -/A | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036222 | TGGGCCCGGCCAGGG[-/A]ACTGGAGTTTTGTCT | 23510 |
rs34581230 | in-del | -/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059636 | AGCAGCAATCCCAGG[-/C]CCCCGTTCAAGGGGT | 23510 |
rs34600095 | in-del | -/A | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041731 | CAAACATTTAACTTG[-/A]AAAGCCCCCTGGGGC | 23510 |
rs34603178 | snp | A/G | 0.362523 | 0.223246 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041097 | GGCATGGTGGCTCAC[A/G]CCTGTACTCCCAGCA | 23510 |
rs34680617 | snp | C/T | 0.378372 | 0.214524 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031909 | AGCTGGGAACTCAGG[C/T]GCCCGCCACACCCAG | 23510 |
rs34787650 | in-del | -/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037421 | CAGACTTTTCCTACA[-/G]GGATTTAAGCCACAT | 23510 |
rs34816922 | in-del | -/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037773 | CCATGTTCAGGCTGG[-/T]ATGCAGTGGCCCACG | 23510 |
rs34891561 | snp | G/T | 0.378765 | 0.214288 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031756 | CTATAAACTAGGGGG[G/T]TTTTTTTGTTTTGTT | 23510 |
rs34981433 | in-del | -/A | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040886 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 23510 |
rs35028659 | in-del | -/C | 0.107694 | 0.205546 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036330 | GTTTCACCGTGTTAG[-/C]CAGGATGGTCTCAAT | 23510 |
rs35041866 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060505 | CTAACCAGACAACAG[C/T]GCGACAGCCAAGACC | 23510 |
rs35059350 | in-del | -/T | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051595 | CCACCATGCCCGACC[-/T]TTTTTTTTTTTAAAT | 23510 |
rs35221374 | snp | A/T | 0.166832 | 0.235761 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058619 | GCCTGGCCAACATGG[A/T]GAATCCCCTTCTCTA | 23510 |
rs35243785 | in-del | -/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033123 | ACTTTTATTTAATAA[-/T]TTTTTTTCTTTTTTT | 23510 |
rs35288670 | in-del | -/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036224 | GGCCCGGCCAGGGAA[-/C]TGGAGTTTTGTCTGC | 23510 |
rs35313674 | in-del | -/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032393 | CCCTGTGAGCAGTCA[-/G]GGGACACGTTCTGGA | 23510 |
rs35326239 | in-del | -/A | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037346 | AAAAAAAAAAAAAAA[-/A]GAAATGGCAGAAATG | 23510 |
rs35413070 | in-del | -/A | 0.378372 | 0.214524 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031828 | GGAGTGCAATGGCGC[-/A]ATCTCGGGTCACTGC | 23510 |
rs35552011 | snp | A/T | 0.106987 | 0.205054 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033669 | GGTGTCCAGGCAACC[A/T]CCAAGCGGACCCTCG | 23510 |
rs35555554 | snp | C/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048862 | ATTTCAGTTACACAG[C/G]TACGGCATTTTCTCC | 23510 |
rs35594725 | in-del | -/A | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041197 | AACCCCGTCTCTACC[-/A]AAAATACAAAAAATT | 23510 |
rs35794705 | in-del | -/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051301 | TTTTTTTTTTTTTTT[-/T]GGCGACAGAGTCTCC | 23510 |
rs35843328 | in-del | -/G | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046550 | GCTGCCGAAGGGGAA[-/G]GGCGCAGCCCCGCAG | 23510 |
rs35875644 | in-del | -/T/TTTTTTT | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056971 | TTTTTTTTTTTTTTT[-/T/TTTTTTT]GGAGACAGAGTCTCG | 23510 |
rs35903673 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058418 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCAGGGAG | 23510 |
rs35928207 | snp | G/T | 0.3742 | 0.216966 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037534 | AATGAGAAAATTAAA[G/T]TCTCAAGACAGTAAA | 23510 |
rs35962822 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036481 | TGCTGAACAATCCAA[A/G]AGGGCATAAAAAATA | 23510 |
rs36040467 | snp | A/T | 0.132409 | 0.220618 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040981 | ATCTTTGAATGAATA[A/T]GCAAATGAACTCTGG | 23510 |
rs55642052 | snp | C/T | 0.079617 | 0.182947 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038723 | TCAGTAAGTGGCGCC[C/T]ACACAGCCCGTCAGA | 23510 |
rs55720441 | snp | C/T | 0.0296464 | 0.118086 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062088 | ATGTTAAGATTGCCA[C/T]ATGAATGTTCACTGT | 23510 |
rs55732969 | snp | A/G | 0.0150606 | 0.0854603 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063325 | ACAGCAGCTGGGCTG[A/G]GTTCCCAGTCGGAGC | 23510 |
rs55803711 | snp | G/T | 0.368119 | 0.220336 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037237 | TACTCCCAGCTACTC[G/T]GGAGGCTGAGGCAGG | 23510 |
rs56104781 | snp | A/T | 0.395568 | 0.203249 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059117 | ATAAATAAATAAAAT[A/T]ATAATAATAATAAAT | 23510 |
rs56229756 | in-del | -/A/AA | 0 | 0 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041463 | AAAAAAAAAAAAAAA[-/A/AA]CAAAACGAAAATTTA | 23510 |
rs56267297 | snp | C/T | 0.399432 | 0.200425 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050901 | CAGGCTGGTCTCAAA[C/T]GTCTGGCCTCACATG | 23510 |
rs56294526 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051748 | CAAGAACAAGGATAC[A/T]GTTTTATGTAACCAC | 23510 |
rs56310455 | in-del | -/A | 0.426507 | 0.177046 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037364 | AAAAAAAAAAAAAAA[-/A]GAAATGGCAGAAATG | 23510 |
rs57081510 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038286 | ATTACAGGCGCCCCC[C/T]GCCCCACCACCACGC | 23510 |
rs57101004 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056943 | TCTGTTTCTTTTTTT[C/T]TCTTTTTTCTTTTTT | 23510 |
rs57813751 | snp | C/T | 0.397813 | 0.201621 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057417 | ATCTTTTGTGATACT[C/T]TGAATTTTGTACTTA | 23510 |
rs58036933 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056985 | TTGGAGACAGAGTCT[C/T]GCTGTGTTGACCAGG | 23510 |
rs58323152 | in-del | -/T | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036055 | GCTAATTTTTTTTTT[-/T]CTTTTTCTTCTTCCC | 23510 |
rs58586812 | in-del | -/AT | 0.5 | 0 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045664 | TCAGAGTTTAAGGTT[-/AT]CTCTCTTGTTCCCTG | 23510 |
rs58708921 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057266 | GACTCCTATTTCTTA[A/G]AATAGTATTTTTTGT | 23510 |
rs60135053 | snp | A/G | 0.0869089 | 0.189476 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047657 | GTAGATCGGTCCCCA[A/G]AGTCCTGAGACACGC | 23510 |
rs60368551 | snp | C/G | 0.161924 | 0.233971 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042890 | CAACTCAAAAAAAAA[C/G]AAAAAAAGACAGTGT | 23510 |
rs60660596 | snp | A/G | 0.230074 | 0.249205 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053133 | GAACTGTTAAGGAGG[A/G]TTGTTTCAAGTGGGC | 23510 |
rs61031996 | in-del | -/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031763 | CTAGGGGGGTTTTTT[-/T]GTTTTGTTTGTTTGT | 23510 |
rs61410279 | snp | C/T | 0.078151 | 0.181571 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038275 | AAGTAGCTGGGATTA[C/T]AGGCGCCCCCCGCCC | 23510 |
rs61549768 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044961 | ATTTTAAAGTTACCA[A/G]GGAACCAAGCACCCT | 23510 |
rs61695347 | snp | A/G/T | 0.182321 | 0.253841 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050997 | TTTTTTTTTTGAGAC[A/G/T]GAGTCTTGCTCTGTT | 23510 |
rs61750318 | snp | A/G | 0.000527035 | 0.0162247 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062154 | CCTATAACTACGGCA[A/G]TGAGGATCAGGCAGA | 23510 |
rs62086352 | snp | A/G | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038177 | TCAGGCTGGAGTGCA[A/G]TGGCACGATCTTGGC | 23510 |
rs62086353 | snp | A/C | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043630 | AAAAAAAAAAAAAAC[A/C]AACCCCAGCTCTCTT | 23510 |
rs62086354 | snp | C/T | 0.039522 | 0.134904 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043723 | ATAAAGACATTTCCA[C/T]CCAGATTGTGTTTTA | 23510 |
rs62086355 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043814 | AGAGCACTCTCTAGG[C/T]TAAAATTTACTTATG | 23510 |
rs62086356 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044287 | CTCGGCTCACTGCAA[A/G]CTCCGCTTCCCGGGT | 23510 |
rs62086357 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045384 | GGTTTTCAGATCAAC[A/C/T]GGTCTGACCAAAATT | 23510 |
rs62086358 | snp | A/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060230 | GAATAGAGTAAATAC[A/T]ATTTTTTTTTTTTTT | 23510 |
rs62086359 | snp | A/T | | | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060750 | GAGTAAATATGATTT[A/T]ATACGGATTATGCCT | 23510 |
rs62087560 | snp | A/T | 0.0298908 | 0.118541 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063569 | TGTCGAATTGAGGTT[A/T]TAGGTAAAGCATAGA | 23510 |
rs62087561 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065708 | GGGAGCAGGGAGCCA[C/T]GGGATGCTGAGAGAG | 23510 |
rs67926907 | in-del | -/GTCT | 0.0150606 | 0.0854603 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064590 | TCCCTAGGACCCTCA[-/GTCT]TCCTTGTTTCTCTGT | 23510 |
rs71159417 | in-del | -/A | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050991 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 23510 |
rs71159419 | in-del | -/AA | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053883 | GTGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 23510 |
rs71159420 | in-del | -/TGTGTGTG | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062737 | CCACGATTTAGAAGC[-/TGTGTGTG]TGTGTGTGTGTGTGT | 23510 |
rs71159421 | in-del | -/A | 0.375 | 0.216506 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066196 | GACTCCATCTCGGGG[-/A]AAAAAAAAAAAAAAA | 23510 |
rs71361642 | in-del | -/G | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036411 | AGGCGTGAGCCACCG[-/G]CGCCCTGCCCAATTA | 23510 |
rs71361644 | in-del | -/GG | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061871 | CGCTGACGGGGGGGG[-/GG]ACTTCAGAGCTTGGG | 23510 |
rs71361645 | in-del | -/AGAC | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063813 | TGCACTGAGTCAGAC[-/AGAC]AAGTGGGAGCTGTAG | 23510 |
rs71380858 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033206 | ACTCCTGGGCTCAAG[C/G]AATCCCCCCACCTCA | 23510 |
rs71380859 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046239 | AGGGGCCTTCCACCA[C/T]GCCCAGCTAATTTTT | 23510 |
rs71380860 | snp | C/G | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058880 | AGGCGGGTGGATCAC[C/G]AGGTCAGGAGATCGA | 23510 |
rs71380861 | snp | A/G | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058882 | GCGGGTGGATCACGA[A/G]GTCAGGAGATCGAGA | 23510 |
rs71380862 | snp | C/T | 0.0307314 | 0.120089 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062290 | TCTGGCTTGCTTGTT[C/T]GCACCCCCTCCGTGG | 23510 |
rs71380863 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064683 | ACACCTATGCGCCAC[A/G]TTTTACAGCTGTAAA | 23510 |
rs71380864 | snp | A/G | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065726 | GATGCTGAGAGAGGA[A/G]GCCCGAGAGGACACC | 23510 |
rs71380865 | snp | C/T | 0.0244538 | 0.107838 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066237 | ACCCAGGCTAGAGTG[C/T]AGTGGTGCAATCTCG | 23510 |
rs72631377 | snp | A/T | 0.330714 | 0.236612 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057513 | TAATATGGAAGGAAA[A/T]CTTTGAAATCCTTAG | 23510 |
rs72844533 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049400 | GTTTTACAGATTTCA[A/G]TTTTGTTTGACATTT | 23510 |
rs73367023 | snp | G/T | 0.0998734 | 0.199905 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034554 | GTGTTCAACCATAGT[G/T]CCCAAACACGGCCCT | 23510 |
rs73367047 | snp | C/T | 0.107341 | 0.205301 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047817 | CCCCGCCCTTCGTTC[C/T]CTGAGACTCCTTCCC | 23510 |
rs73367072 | snp | C/G | 0.109461 | 0.206758 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064615 | TTCTCTGTATCTGTA[C/G]CATAGCATAGAACCC | 23510 |
rs73995733 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033806 | AAGTGCGCGCGGCAG[G/T]GACGGACCCACTCCA | 23510 |
rs73995734 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033843 | GCGCCTCTGTCAGGC[C/T]TTCTCTAGGAAAAGG | 23510 |
rs73995744 | snp | A/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047968 | GCCGGTGCCAGATGC[A/T]TCCAGAACTGGGTCA | 23510 |
rs73995745 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056229 | GTGGCTTTGTAGTTG[A/G]TTTGCAGATTACCAC | 23510 |
rs73995746 | snp | C/T | 0.103919 | 0.20288 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061863 | TAATCCTGCCGCTGA[C/T]GGGGGGGGACTTCAG | 23510 |
rs74993944 | in-del | -/C | 0.331179 | 0.236453 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062564 | TTGGAAGGTATTTTG[-/C]ATTTATTCTTTAAAA | 23510 |
rs75472326 | snp | A/C | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036727 | TGCGCTTTCACTTGG[A/C]TGTCGTCTGCATCCT | 23510 |
rs75533478 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060247 | TTTTTTTTTTTTTTG[G/T]AAAGTCAAATCCCTT | 23510 |
rs75583122 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052260 | AGAGATATTTCCTAG[C/T]AGAAGGAGAGAGATT | 23510 |
rs75594697 | snp | A/C | 0 | 0 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043613 | TGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 23510 |
rs75643864 | snp | C/G | 0.320575 | 0.239832 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041532 | CTCAGGAGGCTAAGA[C/G]AGAAGGATGGCTTGA | 23510 |
rs75930743 | in-del | -/A | 0.0103295 | 0.0711199 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065181 | CGTGCTCTGGGAAAT[-/A]AGACAGGAGTGGTAT | 23510 |
rs75985517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053325 | AATGAGAAGATTGTC[A/G]CTGCTTACCAGATGG | 23510 |
rs76204087 | snp | A/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036696 | TCCAAGTAAACTGCA[A/T]TTTTTCTCACATCCC | 23510 |
rs76241645 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051944 | CAAGTCTTTAAATGG[A/T]TGCCTTTTATATTGT | 23510 |
rs76245783 | snp | G/T | 0.299411 | 0.245069 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065294 | AGGACTCTGGGTTCT[G/T]AAGATTTCTGGGAGC | 23510 |
rs76335024 | snp | G/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050992 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 23510 |
rs76781319 | snp | A/C | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050736 | TGAAGTAATTTAAAA[A/C]TTCAAAATAAGCAAG | 23510 |
rs76971441 | snp | A/C | 0 | 0 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043611 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 23510 |
rs77396576 | snp | A/G | 0.011026 | 0.0734264 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062104 | ATGAATGTTCACTGT[A/G]TTCTTGGTTCATCAG | 23510 |
rs77454968 | snp | C/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049407 | AGATTTCAATTTTGT[C/T]TGACATTTTCATCAG | 23510 |
rs77532229 | in-del | -/G | 0.320335 | 0.239902 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043915 | GCAACTTGCTCCAGA[-/G]TTTTACAAACTTAAA | 23510 |
rs77694486 | snp | G/T | 0.293294 | 0.246223 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056178 | GTTTTCTTCCATCTA[G/T]CTGACAGCTCAAAGG | 23510 |
rs77801582 | snp | A/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036695 | CTCCAAGTAAACTGC[A/T]TTTTTTCTCACATCC | 23510 |
rs77873758 | snp | A/G | 0.5 | 0 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066165 | GAAAGAGACAAGGGG[A/G]GGAGTGTGAGATTTT | 23510 |
rs77925834 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063808 | GCATCCTGCACTGAG[A/T]CAGACAAGTGGGAGC | 23510 |
rs78046671 | snp | C/T | 0.00153905 | 0.0276976 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036084 | CCTGAGACGGAGTCT[C/T]GCTCTGTCACCCAGG | 23510 |
rs78205686 | snp | C/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057557 | GATAGCTATACCTCT[C/T]TTTTTTTTTTTTTTT | 23510 |
rs78363853 | snp | A/C | 0.5 | 0 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040886 | GCAAGACTCCGTCTC[A/C]AAAAAAAAAAAAAAA | 23510 |
rs78507102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054499 | TAAGTAATTGAAAGT[C/T]CTTGCCCTCAAGAAG | 23510 |
rs78548907 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051945 | AAGTCTTTAAATGGT[C/T]GCCTTTTATATTGTT | 23510 |
rs78799857 | snp | C/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057574 | TTTTTTTTTTTTTTT[C/T]CTCGAGGCAGAGTCT | 23510 |
rs78830045 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053372 | GGGCACTTTAGGTCT[A/G]AAACCTGTTCTCTGC | 23510 |
rs79109885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053488 | CCCTGTCGCCCAGGC[C/T]GGAGTGCAGTGGTGC | 23510 |
rs79204273 | snp | A/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060232 | ATAGAGTAAATACAA[A/T]TTTTTTTTTTTTTGG | 23510 |
rs79509828 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051943 | GCAAGTCTTTAAATG[A/G]TTGCCTTTTATATTG | 23510 |
rs79696272 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044456 | ATGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 23510 |
rs79744180 | snp | A/G | 0.095934 | 0.196885 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052905 | TCTCAAAAAATAAGT[A/G]AATAAATAAATAAGC | 23510 |
rs79812953 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037513 | ATTACAATCCTGATA[C/T]TTGTAAATGAGAAAA | 23510 |
rs80127497 | snp | G/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050991 | CTTTTTTTTTTTTTT[G/T]GAGACGGAGTCTTGC | 23510 |
rs80319906 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035408 | GCTGGTACCTGGAAC[A/G]AGTTCAACATCCAAA | 23510 |
rs111249217 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034446 | CACCCCAGGTGGGAC[A/T]CGAACCCACAATCCC | 23510 |
rs111299840 | snp | C/G | 0 | 0 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039066 | TCATCTTCTCCATCT[C/G]GAAAGAGGGGGAATG | 23510 |
rs111311177 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032420 | TGGAACTAGGGCGGC[A/G]GCAGCAGGGATGGGG | 23510 |
rs111328340 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049144 | GGGCGCTGACAAAGA[C/T]GGTGAAATCCTGCCC | 23510 |
rs111347972 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033618 | GCGGTAGGAAGGAAA[C/T]TCCTCCAAACCTCAG | 23510 |
rs111352605 | snp | C/T | 0.5 | 0 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044343 | CCCGAGTAGCTGGGA[C/T]TACAGGCGCCCGCCA | 23510 |
rs111447925 | snp | A/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053580 | CGTGTAGCTGGGACT[A/T]CAGGTGTGTGCCACC | 23510 |
rs111538698 | snp | A/G | 0.336245 | 0.234652 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044367 | CCCGCCACCGCGCCC[A/G]GCTAATTTTTTGTAT | 23510 |
rs111556238 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060932 | CTTAGCTTCCACCAC[A/G]GAATCCACTCTGCCT | 23510 |
rs111592562 | snp | A/G | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033877 | CACTCGCTTATGAGG[A/G]GAAGGGATGGCACGG | 23510 |
rs111621296 | snp | A/G | 0.493925 | 0.054776 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044351 | GCTGGGACTACAGGC[A/G]CCCGCCACCGCGCCC | 23510 |
rs111634509 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046137 | GCCTGGGCTGGAGTG[C/T]AGTGGCGTGGTCTCG | 23510 |
rs111665321 | snp | C/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061137 | TGTCCCGTGGGAAGA[C/T]GGAGGGTGTTCCTAT | 23510 |
rs111672862 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065346 | GGAACCAGGCTGGTG[C/G/T]TCTTGCTTGAAAGCG | 23510 |
rs111700738 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049732 | AGTTGTACAAAAATA[A/G]TAAAGGCTTGGCCTC | 23510 |
rs111767927 | in-del | -/CAGA | 0.376394 | 0.215696 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063808 | CATCCTGCACTGAGT[-/CAGA]CAGACAAGTGGGAGC | 23510 |
rs111793371 | snp | C/G | 0.162581 | 0.234218 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041443 | GACAAAAACCTGTCT[C/G]TACCAAAAAAAAAAA | 23510 |
rs111876406 | snp | A/G | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037649 | TTAAATACTTGCATT[A/G]CTCTATGATCTACTA | 23510 |
rs111893561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035216 | TGCAACTATAATCTT[C/T]CCTCCCTTGTTTTAG | 23510 |
rs111938818 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049030 | AATGTACAAGATACA[A/T]AAAGCTATAGCTTTC | 23510 |
rs111985824 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060303 | GGCATTTAAAACAGA[A/C]ATTGCTACATCACTA | 23510 |
rs112073620 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060675 | CGCGCGTGCGAGGGC[A/G]GGTCAGGCTGCACTC | 23510 |
rs112163129 | snp | A/G | 0.0126979 | 0.078662 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064284 | GAGCATGTGGGTCTC[A/G]CTGAGCAGTCATGGA | 23510 |
rs112223260 | snp | A/G | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049667 | GTCTGAAGAAGCAAG[A/G]CATCTCTGACATTCA | 23510 |
rs112269925 | snp | A/G | 0.332568 | 0.235971 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057707 | TGGGATTACAGGCAC[A/G]TGCCACCTCACCTGG | 23510 |
rs112276578 | snp | C/T | 0.330714 | 0.236612 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055913 | GCGGGCGCCTATAAT[C/T]CCAGCTACTTGGGAG | 23510 |
rs112400141 | snp | A/G | 0.5 | 0 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75065966 | TCTCACATGGGTTTC[A/G]GGAGATGACTTAACT | 23510 |
rs112410973 | snp | G/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035111 | AGGTAGCTGCAGCCG[G/T]AGACCGCGTGGCCTA | 23510 |
rs112426241 | snp | C/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055598 | CAGCACTTTGGGAGG[C/T]CGAGGCAGGTGGATC | 23510 |
rs112460242 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049976 | GGGCACCCTGATCTG[A/G]GAGCTTTGGCTCTGA | 23510 |
rs112569307 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043861 | TCAGTCCTGCTTGCC[C/G]CAGAGGGCTGCTAAA | 23510 |
rs112631693 | in-del | -/TTTTTTTTTTT | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056953 | TTTTTTTCTTTTTTC[-/TTTTTTTTTTT]TTTTTTTTGGAGACA | 23510 |
rs112722430 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043542 | CACTTGAACCTGGGC[A/G]GCGGAGGTTGCAGTG | 23510 |
rs112765670 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063133 | CTCCTGTCCAGTGAC[C/T]GAGCCACTGCAAAGC | 23510 |
rs112777332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054393 | GAAAGAAAGATGTTA[C/T]GGCACATCTATTTCA | 23510 |
rs112828398 | snp | A/G | 0.493925 | 0.054776 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044355 | GGACTACAGGCGCCC[A/G]CCACCGCGCCCGGCT | 23510 |
rs112832617 | snp | A/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034977 | CGCTCGGGGGTGACT[A/T]GGCGGGCGGCTGGGG | 23510 |
rs112919118 | snp | A/G | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053832 | AGTCTCATGGGGTAC[A/G]CTTCAGCAGCTGCTT | 23510 |
rs112922015 | snp | A/G | 0.5 | 0 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042540 | TGACCTGGAGGTGAG[A/G]GTCTCATTCCAGGAT | 23510 |
rs112940908 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040676 | GGATCACCTAAGGTC[A/G]GGAGTTCGAGACCAG | 23510 |
rs113034131 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034426 | GCGAGCACAGCCCCT[C/T]TCGACACCCCAGGTG | 23510 |
rs113037769 | snp | C/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052784 | CTGTAGTCCCAGCTA[C/T]TTGGGAGACTGAGGC | 23510 |
rs113050129 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031439 | TGAATGACATAAGAA[A/T]GGTCTCAGTAGATTG | 23510 |
rs113065268 | in-del | -/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037237 | TACTCCCAGCTACTC[-/T]GGAGGCTGAGGCAGG | 23510 |
rs113076798 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043566 | TGCAGTGAGCTGAGA[C/T]AGCGCCATTGCACTC | 23510 |
rs113211160 | snp | C/T | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062367 | GCCAGCGTTGCATTT[C/T]CCCCTCGTTTTGTTA | 23510 |
rs113406774 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048739 | TGCAAACTCCCACTG[A/G]TGTTGGCCTTGAGCT | 23510 |
rs113449956 | snp | A/G | 0.0403705 | 0.136218 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053129 | TTTGGAACTGTTAAG[A/G]AGGGTTGTTTCAAGT | 23510 |
rs113524007 | snp | A/T | 0.100944 | 0.200705 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033124 | CTTTTATTTAATAAT[A/T]TTTTTTCTTTTTTTT | 23510 |
rs113542780 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039564 | CTCAGCCACTGAATG[A/G]TCAGGACACGCCACC | 23510 |
rs113613492 | snp | A/G | 0.16028 | 0.233346 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051305 | TTTTTTTTTTTTGGC[A/G]ACAGAGTCTCCCTCT | 23510 |
rs113775187 | snp | A/G | 0.404733 | 0.196361 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051195 | AGCCAGGATGGTCTC[A/G]TCTCGATCTCCTGAC | 23510 |
rs113797879 | snp | A/C | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046209 | TGCCTCAGCCTCCCG[A/C]GCAGCTGGGATTATA | 23510 |
rs113863274 | snp | A/G | 9.88875e-05 | 0.00703093 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053048 | GTTTTACAACATCGC[A/G]TCCCTTGTGCGGCTG | 23510 |
rs114017223 | snp | C/G/T | 0.0460506 | 0.144768 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033782 | GGTATCTTCCCGCCC[C/G/T]CTCACCAAAAGTGCG | 23510 |
rs114077345 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052825 | TTTGAACGCAGGAGG[C/T]GGAGGTTGCCGTGAG | 23510 |
rs114110296 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042753 | AAGAGCTCTTAGAGA[G/T]AATCCTTTAAATCTT | 23510 |
rs114171186 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033313 | TTAAATGTGTGTAAC[A/T]TTTTAAAATGTGCTT | 23510 |
rs114429054 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055354 | GGCACCATGCCTGGC[A/G]TAAGTTTACTTTTAA | 23510 |
rs114435031 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041265 | GGGGATGAGGTGGGA[A/G]GAAGGCTTGAGCCCG | 23510 |
rs114547131 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031621 | CCGAGGCCTGCCTGC[A/G]TCTGGACAGGAAACT | 23510 |
rs114649082 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033744 | TCGCTAAGTAAGGAT[G/T]GGGGCAGGTCCCTGC | 23510 |
rs114651322 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035058 | TGAAGCTGCGGCACG[C/T]CGGAGCGTTTAATGG | 23510 |
rs114688599 | snp | A/G | 0.0448719 | 0.142907 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031690 | GGTCAGCTCCCATCC[A/G]TCCACCTCCCCCAGC | 23510 |
rs114786710 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049843 | TGTATCATTACTTGC[C/T]TCATCTTTGTGGTTT | 23510 |
rs114948535 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059704 | AATAACCACGGGAGA[C/T]GGCTACGGCCAGGTG | 23510 |
rs115136358 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033445 | AAGAACTTGTTCCCC[C/T]TGGTTGTACATTCCC | 23510 |
rs115201385 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044638 | TGAGCCACCGCGCCC[A/G]GCCTGCATTTTAAGA | 23510 |
rs115296203 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033981 | CCCACCTGGGGTAGA[C/G]GTGAAAGTTCCTTTT | 23510 |
rs115469710 | snp | C/T | 0.040671 | 0.13668 | utr-variant-3-prime, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038867 | ACACCCAGAACTGTA[C/T]AATTATTATTTTTAA | 23510 |
rs115504269 | snp | C/T | 0.040671 | 0.13668 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041222 | AAAATTAGCCAGGCA[C/T]GGTGGTGCTGTGGTC | 23510 |
rs115521855 | snp | A/G | 0.0252325 | 0.109451 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048576 | ATTTTTATCTACTCT[A/G]TATCCTCCTTGTGGT | 23510 |
rs115540755 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045057 | ATTTTCCTAAGCGTC[G/T]ACTGGCTTGACAGAG | 23510 |
rs115756741 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037710 | GTTGCTCAGGTCTGC[G/T]AACCATAGTAAATAG | 23510 |
rs116063598 | snp | A/T | 0.0422008 | 0.138995 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066301 | AATTCTCCCTCGGCT[A/T]CCTGAGTAGCTGGGA | 23510 |
rs116075492 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033056 | AAGCACAATGGTAAC[C/T]GACGCTGCCCTTGGC | 23510 |
rs116483912 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052243 | TTTACCGAAAATAGC[A/G]AAGAGATATTTCCTA | 23510 |
rs116725889 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033988 | GGGGTAGAGGTGAAA[A/G]TTCCTTTTACGGAAT | 23510 |
rs116972075 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060705 | CAGGGTCTCGGTCGC[C/T]GCCACTCGCCACCCT | 23510 |
rs116998886 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038098 | TTCAAATGCAAAAAG[C/G]TGTAAGTTAACTGTG | 23510 |
rs117008429 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046650 | TGAAGTCTGCCGCGC[C/T]GGGAGCGGACTGCAC | 23510 |
rs117189411 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040227 | CAAGGACAGTGAGTC[A/G]TCGCCAATACACCCA | 23510 |
rs117259305 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062529 | ACTAATTACTACAGG[A/G]TAGGATTTCTGAACT | 23510 |
rs117302657 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041912 | GGGTGAACCGGCCCA[A/G]GTCAGAAACAGAGCA | 23510 |
rs117363271 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036458 | TTAATGCATGTACAA[C/T]GCAAAAATGCTGAAC | 23510 |
rs117369617 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034949 | GGCTCAGAGACTAGT[C/G]CAGGTGCCGCTCCGC | 23510 |
rs117827586 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040615 | TGTTAGCCGGGTGCG[A/G]TGGCTCATGCCTGTA | 23510 |
rs137917167 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033416 | TATATATATATTTCT[A/G/T]CTATTACAACTGGAA | 23510 |
rs137974012 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058365 | AAAAATTAGCTGGGC[A/G]TAGTGGCACATGCCT | 23510 |
rs138103208 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040882 | CAGAGCAAGACTCCG[C/T]CTCAAAAAAAAAAAA | 23510 |
rs138253735 | snp | A/G | 4.95413e-05 | 0.00497677 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042215 | ACCAAGCCAGCCTTG[A/G]CCACATTGGCCTTGT | 23510 |
rs138283109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049586 | TTCAGGAGTTCTTTC[A/C]GAATCTCCAGAATTG | 23510 |
rs138307477 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041584 | GTAAGCTGAGATTGC[A/G]CCACTGCACTCCACC | 23510 |
rs138310601 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054438 | TCATATGTTTGTCGT[A/G]TGTTTGAATGGCCAT | 23510 |
rs138589205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061866 | TCCTGCCGCTGACGG[G/T]GGGGGACTTCAGAGC | 23510 |
rs138660863 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057234 | GCTGGGATTACAGGC[A/G]TGAGCAACCATACCC | 23510 |
rs138763303 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054611 | GAGATCGAGACCATC[C/G]TGGCTAACACGGTGA | 23510 |
rs138782296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033849 | CTGTCAGGCCTTCTC[C/T]AGGAAAAGGGGACAC | 23510 |
rs138851328 | snp | C/T | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045254 | AGGGTAATAGAATAT[C/T]ACAAGGCAAGTGGAG | 23510 |
rs138972436 | in-del | -/T | 0.00798878 | 0.0628851 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033130 | ACTTTTATTTAATAA[-/T]TTTTTTTTCTTTTTT | 23510 |
rs139115368 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048120 | GTCGCAGAACTTTTA[C/T]CTGTTAACAGTCACT | 23510 |
rs139396427 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062301 | TGTTCGCACCCCCTC[C/T]GTGGGCTTTTCCTGA | 23510 |
rs139430113 | snp | A/G | 0.000164965 | 0.00908048 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042515 | ATGGGGTTCCCTCTC[A/G]GAAACATACTGACCT | 23510 |
rs139610516 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055123 | GCAGTGGCATGATCT[C/T]GGCTTACTGCAACCT | 23510 |
rs139620153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051774 | ACCACAGACAGTACA[C/G]TTATCAAACTCAGGA | 23510 |
rs139684261 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054827 | AAAAAAAAAAAAGAA[A/G]CTTGAAGTATAGCCA | 23510 |
rs139693159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033899 | ATGGCACGGCCACGT[A/G]CCCCAAGCCCCAGTG | 23510 |
rs139761287 | snp | A/G | 3.2956e-05 | 0.00405918 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042537 | TACTGACCTGGAGGT[A/G]AGGGTCTCATTCCAG | 23510 |
rs139824435 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043159 | CCAGGAGGCAGAGGT[G/T]GTAATGAGCTGAGAT | 23510 |
rs139838680 | snp | C/T | 0.000444814 | 0.0149067 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053015 | TGTCCTTGTTCCAGG[C/T]GTGCTGGAGGAAGCG | 23510 |
rs139896233 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064450 | TTCAGAAGTGATGTC[C/G]TGTGTGCTCCACAGC | 23510 |
rs139924151 | in-del | -/TAATT | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046247 | TCCACCACGCCCAGC[-/TAATT]TTTTGTATTTTTAGT | 23510 |
rs140053200 | in-del | -/C | 0.0158469 | 0.0875917 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041809 | AGTTCTGGGCTGTAG[-/C]GCGTTATGCCGATCG | 23510 |
rs140105966 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031517 | GTGCTTGAGATGGGC[C/T]TGAAGGGAGGGGAGA | 23510 |
rs140117230 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035105 | TCTAGGAGGTAGCTG[C/G/T]AGCCGGAGACCGCGT | 23510 |
rs140171348 | snp | A/C/G | 4.94474e-05 | 0.00497205 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053051 | TTACAACATCGCGTC[A/C/G]CTTGTGCGGCTGGTT | 23510 |
rs140173009 | snp | A/C/G | 0.0193847 | 0.0965802 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046684 | ACACGGCTTGTGGCA[A/C/G]CGCCTACATCAGCGG | 23510 |
rs140311695 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039951 | TTTGAAATTCGTCCA[C/T]GTTGTTGCATTTATT | 23510 |
rs140527005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054422 | CACATCCTGCCATTC[A/G]TCATATGTTTGTCGT | 23510 |
rs140531818 | snp | A/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048361 | TTCACCTTTAAGTTC[A/T]CAACTTAAAGGCACT | 23510 |
rs140757605 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039677 | ATTTGAATACTACTT[C/G]GGTAATTTTTCTAAT | 23510 |
rs141097803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057000 | CGCTGTGTTGACCAG[A/G]CTGGAGTGCAGTGAT | 23510 |
rs141160534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75061074 | TTTTTAATGTATTCT[G/T]TGTGAAACTAAAATG | 23510 |
rs141339135 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033888 | GAGGGGAAGGGATGG[A/C/G]ACGGCCACGTGCCCC | 23510 |
rs141432417 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049140 | CTTGGGGCGCTGACA[A/C]AGATGGTGAAATCCT | 23510 |
rs141535456 | snp | A/T | 3.3018e-05 | 0.00406299 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042253 | CCAGTCGATAGCTGG[A/T]GGATTCTCAGGTAAA | 23510 |
rs141670304 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055157 | CCTCCCAGGTTCAAG[C/T]GATTCTCATGTCTCA | 23510 |
rs141677302 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061442 | TTGAGTCCTGGAGTT[C/G/T]GGAGACCAGCCTGGG | 23510 |
rs141715404 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061938 | GAGGCCTCACCAATG[A/G]TGCCCTGATGAAGAA | 23510 |
rs141770830 | snp | C/T | 0.000148247 | 0.00860822 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040126 | TCCACCTGGGCAGTA[C/T]ATTTATCCTCTGGCA | 23510 |
rs141855138 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065274 | CTGTATTGTTCCAGC[A/G]CTCCAGGACTCTGGG | 23510 |
rs141984042 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062461 | TATGAACCTAAAAAG[A/C/G]GTAGACTTTCTCCAT | 23510 |
rs142238434 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050643 | CCTCAAGCATTTATC[C/T]TTTGTGATACAAAAA | 23510 |
rs142351398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044902 | TTTCTCAGGACAGCC[G/T]GTTTCCTGTTGTGGA | 23510 |
rs142354988 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031183 | AGACGTGGTCCCTGT[C/T]CTCAAGGGACTCAGA | 23510 |
rs142463802 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035101 | CCTCTCTAGGAGGTA[A/G]CTGCAGCCGGAGACC | 23510 |
rs142595401 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033530 | GTCTGTTCTCCTTCA[C/G]TTCCTACGCTACTTT | 23510 |
rs142597775 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054936 | GTCGTGCTCCACCAT[A/G]ACTACCTGTGTTGTA | 23510 |
rs142618026 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032331 | GACTGCTCTGCCCAC[A/G]ACAGAACGAGGAGAC | 23510 |
rs142693683 | in-del | -/AAG | 0.00512528 | 0.0503624 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053126 | GTATTTGGAACTGTT[-/AAG]GAGGGTTGTTTCAAG | 23510 |
rs142756079 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054632 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 23510 |
rs142871272 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063659 | GTCCTTTGTTGTGGT[C/T]GGAGGTTGGTGATCA | 23510 |
rs142928153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046441 | CCTAGAACAGATCAT[A/G]CGCATAGGAGGTGCT | 23510 |
rs142991058 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050075 | GAAAGAGGAATTGCT[C/G]TCTCTCTCTTTTTTT | 23510 |
rs143068192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042938 | GTAATTCAAGGTGTG[C/T]GGCCAGGCGCAGTGG | 23510 |
rs143128468 | snp | G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043381 | CTTTGGGAGGCTGAG[G/T]TGGGTGGATCACTTG | 23510 |
rs143156940 | snp | C/T | 0.000181274 | 0.00951863 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053045 | GGAGTTTTACAACAT[C/T]GCGTCCCTTGTGCGG | 23510 |
rs143257987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049146 | GCGCTGACAAAGATG[A/G]TGAAATCCTGCCCTG | 23510 |
rs143272748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039727 | CAGCTTTGTTGAGGT[A/G]TATCTGAAATATGAT | 23510 |
rs143500616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75032845 | GCTGGATCCCAGCAA[C/T]GGACAAGTTAGTTAA | 23510 |
rs143541928 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039041 | ATCTGATCAAATGGA[A/G]TTAAGTTCTTCATCT | 23510 |
rs143613826 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037511 | TCATTACAATCCTGA[C/T]ATTTGTAAATGAGAA | 23510 |
rs143699289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055903 | GAGTGTGGTAGCGGG[C/T]GCCTATAATCCCAGC | 23510 |
rs143756489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056619 | TTTTTGATGTTAACT[A/G]TCTTTCCATCTGTCC | 23510 |
rs143789920 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041666 | TAGAAAAAAAGTCAG[A/T]TTGTTCCAAAGGGAG | 23510 |
rs143909039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037998 | AGGTTGCAGTGAGCC[A/G]AGATCGTCCCACTGC | 23510 |
rs143915019 | snp | C/T | 0.000115562 | 0.00760051 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042221 | CCAGCCTTGGCCACA[C/T]TGGCCTTGTAGTAAG | 23510 |
rs144012337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039153 | ACCAGGTGAAAGATG[C/T]GTGGTCATGAAAGAG | 23510 |
rs144034370 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058478 | CACTGCACTCCAGAC[G/T]GGGCAACAGAGCGAG | 23510 |
rs144230925 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031120 | AAAAATAAAATAAAA[C/T]AAAATTGGAATGATA | 23510 |
rs144466941 | snp | A/C/G/T | 7.69299e-05 | 0.00620165 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047570 | GCTGCCAGGAGGACC[A/C/G/T]GGAGCTGGACTCAGA | 23510 |
rs144634308 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039001 | TTTGGTTTCTGGGAA[A/G]GCTTCATTCAAGTCC | 23510 |
rs144678885 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063202 | CAAAACTAAAGGAAC[A/T]CCCTCCCCACCTGCA | 23510 |
rs144818105 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050802 | CCCAGATTAACCAAT[C/T]TTCAATGTTATTTTT | 23510 |
rs144818540 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035875 | AAACTCCAGTCCCTA[A/G]CCTCAAGGGCAGTGG | 23510 |
rs144857095 | snp | A/G | 0.00144788 | 0.0268672 | utr-variant-3-prime, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038884 | ATTATTATTTTTAAT[A/G]TCCAGAATGTGTAAT | 23510 |
rs144924411 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048182 | TTTTGGAAAGAGGTT[A/T]CTGTTTGCCGCTGCA | 23510 |
rs144981192 | snp | A/G | 6.63306e-05 | 0.00575855 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059527 | CCCCGTGAAGCACGT[A/G]TACAGAGTCCTGCAG | 23510 |
rs145062395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052095 | CATGACTAGTTCCAG[C/G]AACTAAGTGACATAT | 23510 |
rs145096735 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050147 | TAATGGGAATAGTAC[A/G]TACAGTGAATTCCTT | 23510 |
rs145131285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053903 | ACAGAGTCTCACTCT[C/T]TCCCCCAGGCTGGCC | 23510 |
rs145356520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060703 | CTCAGGGTCTCGGTC[A/G]CCGCCACTCGCCACC | 23510 |
rs145520008 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031644 | AGGAAACTTGTGATT[A/G]AGAGAATGGGCTCTG | 23510 |
rs145586014 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034452 | AGGTGGGACTCGAAC[C/T]CACAATCCCTGGCTT | 23510 |
rs146067407 | snp | A/G | 9.90557e-05 | 0.0070369 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059578 | GCAGATGGTGTCCAC[A/G]ATGTCCGACGGCTGG | 23510 |
rs146138726 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043150 | CACTTGAACCCAGGA[A/G]GCAGAGGTTGTAATG | 23510 |
rs146157441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046471 | TCAATGAATCTTTCT[G/T]GAATGAGTAACCGAA | 23510 |
rs146252726 | in-del | -/AAAATAAAAT | 0.232127 | 0.252548 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031105 | TGAGACTCCGTCTCA[-/AAAATAAAAT]AAAATAAAATAAAAT | 23510 |
rs146259371 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058747 | GAGTTGCAGTGAGCT[A/G]AGATCGCGCCACTGT | 23510 |
rs146327952 | snp | C/T | 3.29777e-05 | 0.00406051 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062233 | CGTCATAGAGCCGAG[C/T]GAAAAGGCGAAGGTA | 23510 |
rs146343520 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045035 | ATAGTCACATAGGTT[C/T]TTTTCTATTTTCCTA | 23510 |
rs146353185 | in-del | -/CAGA | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063809 | ATCCTGCACTGAGTC[-/CAGA]AGACAAGTGGGAGCT | 23510 |
rs146419218 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039514 | TTCTGCAAGTTCCTC[A/G]TCCGAAGACCTACAG | 23510 |
rs146425045 | snp | A/G | 0.00165251 | 0.0286971 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047571 | CTGCCAGGAGGACCC[A/G]GAGCTGGACTCAGAC | 23510 |
rs146461671 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035592 | TTGGGAGGCTGAGGC[G/T]GGCGGATCACGAGGT | 23510 |
rs146585287 | snp | A/G | 0.00159328 | 0.0281798 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053156 | AAGTGGGCTTCTGTC[A/G]GTCGGTCTGTGATTT | 23510 |
rs146827625 | snp | A/C | 0.00045225 | 0.0150306 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059515 | GTCATTGCAGGGCCC[A/C]GTGAAGCACGTGTAC | 23510 |
rs146885302 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057146 | TTTAGTAGAGACAGG[A/G]TATCCCCATGTTGGC | 23510 |
rs146898601 | in-del | -/GG | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061864 | AATCCTGCCGCTGAC[-/GG]CGGGGGGGGACTTCA | 23510 |
rs146909817 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75061013 | GAGTTTAATGCCCTC[A/C]ACTCCAGAAGTATTT | 23510 |
rs146924898 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061149 | AGACGGAGGGTGTTC[C/T]TATTGCCTCCCTTCT | 23510 |
rs146941496 | snp | A/G | 0.0197687 | 0.0974348 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065701 | TGAGGCTGGGAGCAG[A/G]GAGCCACGGGATGCT | 23510 |
rs146993323 | in-del | -/AT/TA | 0.361053 | 0.22398 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045663 | GTCAGAGTTTAAGGT[-/AT/TA]TCTCTCTTGTTCCCT | 23510 |
rs147047016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041328 | CCACTGCACTCCAAC[A/C]TGAGTGACAGAGTGA | 23510 |
rs147134939 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054586 | CGAGACGGGCAGATC[A/G]TGAGGTCAGGAGATC | 23510 |
rs147154361 | in-del | -/AGTA | 0.00478085 | 0.0486577 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054907 | AACTACAGAGTTAAC[-/AGTA]AGAAGGCAGAGTCGT | 23510 |
rs147278817 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041685 | TTCCAAAGGGAGACA[A/G]GAAGGAAGCTAAAAG | 23510 |
rs147284668 | snp | G/T | 0.000313622 | 0.0125185 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042224 | GCCTTGGCCACATTG[G/T]CCTTGTAGTAAGCCC | 23510 |
rs147298280 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034519 | GCGGTAAGACGCTAA[A/C/G]CCCACGTGCTCCTTG | 23510 |
rs147365499 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054723 | GAAGCAGGAGAATGG[C/T]GTGAACCCAGGAGGC | 23510 |
rs147451867 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037966 | AGGCAGGAGAATGGC[A/G]TGAACCCATGAGGTA | 23510 |
rs147461348 | snp | A/C | 8.23784e-05 | 0.00641735 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040148 | CCTCTGGCACGGGAA[A/C]CTTCAGCGCATTAAA | 23510 |
rs147487860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034399 | CTGGCTGCCGGCACC[A/G]AAAGAAACCTTGCGA | 23510 |
rs147754539 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032032 | CTCACAAAGTGCTGG[A/G]ATTACAGGTGTGAGC | 23510 |
rs147843647 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044773 | GGGTCAGATATTAAA[A/C]GACTGCAAAGTCAAA | 23510 |
rs147859911 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049051 | TATAGCTTTCTTACC[A/G]ATAGTTTGTGACAAA | 23510 |
rs147890740 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031413 | TTACAGTAGCAGGAC[C/G]TGAAGCACGATGAAT | 23510 |
rs147947086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75061056 | GCTCTTAAGCAAAGG[A/G]TTTTTTTAATGTATT | 23510 |
rs147964075 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064947 | CCTTGTGCCCAGTCT[C/T]GTTGAGGCGCTTGTC | 23510 |
rs148020009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061372 | CCAGCATGCTGGGCA[C/T]GGTGGTTCACACCTG | 23510 |
rs148051075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037683 | TGCTTTAAACCATCT[C/T]TATTGCCTGACGTTG | 23510 |
rs148175224 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056828 | TACCTGTAGCCCCTC[A/C]CACATGCAGGATTCA | 23510 |
rs148316648 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042020 | CCTAAATTCCTGCAC[C/T]TATTTACAGTTCAAT | 23510 |
rs148545284 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063412 | ACTTTAAGGACGCTG[A/G]AGCCAAGAGGATTGT | 23510 |
rs148579788 | snp | C/T | 8.24314e-05 | 0.00641942 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039105 | TAATGTAAACAGAGA[C/T]GGAAAGCAGAATATC | 23510 |
rs148590001 | snp | C/T | 3.66066e-05 | 0.00427808 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047544 | GCCCAAGTCATTTCT[C/T]TGCCGCCTCTGCTGC | 23510 |
rs148754531 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031150 | ACAGAGAAGATTAGC[A/G]TGGCTCCTTTAAAGT | 23510 |
rs148808947 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035057 | GTGAAGCTGCGGCAC[C/G]CCGGAGCGTTTAATG | 23510 |
rs148813887 | snp | A/G | 0.0107246 | 0.0724382 | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75032609 | GGAGGGGTGCCCAGT[A/G]GTGATGCCCAGGAGA | 23510 |
rs148864133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037310 | AATCGTGCCACTGCA[C/T]TCCAGCCTGGGCGAC | 23510 |
rs148887046 | snp | A/G | 6.5937e-05 | 0.00574144 | stop-gained, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039030 | CCTCAATGGTCATCT[A/G]ATCAAATGGAATTAA | 23510 |
rs148932944 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052556 | ATGAAACCCTGTCTC[C/T]ACTAAAAATACAAAA | 23510 |
rs148985616 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056463 | TGAACATTCTCCCTT[C/T]TTCGTCATTAGCTAA | 23510 |
rs149108925 | in-del | -/A | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033149 | TTTTTTCTTTTTTTC[-/A]AATGAGACTGCATCT | 23510 |
rs149114130 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059565 | AAGAAGAGCTCACGC[A/G]GATGGTGTCCACGAT | 23510 |
rs149342698 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034288 | GGTAAATGACCACCG[A/C]GACTGCAAACAGAGG | 23510 |
rs149411955 | snp | C/T | 3.29826e-05 | 0.00406082 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042640 | TTTAGAGCAAGTTTT[C/T]GCCCAGCCATTTTGG | 23510 |
rs149426575 | in-del | -/T | 0.00712204 | 0.0592478 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036045 | GAGAATAAATGCTAA[-/T]TTTTTTTTTTCTTTT | 23510 |
rs149448845 | in-del | -/C | 0.040671 | 0.13668 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060183 | CAGACTTGTTAAATT[-/C]TGTTGCCTTCAAAAC | 23510 |
rs149873657 | snp | C/G | 0.0023933 | 0.0345097 | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75035269 | CTCCACACCGCGGCT[C/G]CCGGGATCCGAAGCT | 23510 |
rs149907467 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048121 | TCGCAGAACTTTTAT[C/T]TGTTAACAGTCACTG | 23510 |
rs149957614 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052074 | TCAAGTTCAGGAGGT[C/G]TCCAACATGACTAGT | 23510 |
rs150100426 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032353 | CGAGGAGACTGTAGG[A/G]AAGTGTGCATGGCTG | 23510 |
rs150103793 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061806 | TTTGTTGGCAGATGC[A/G]TTCTGTCTTCCCTTG | 23510 |
rs150187875 | in-del | -/CAAGGAAAGTAGTGAT | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064802 | AAAGTTAGATGTAGC[-/CAAGGAAAGTAGTGAT]CACGGGAAGGACTGC | 23510 |
rs150191592 | in-del | -/CT | 0.0103295 | 0.0711199 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032381 | CTGGCAACTGACCCC[-/CT]GTGAGCAGTCAGGGA | 23510 |
rs150354933 | snp | C/G/T | 1.66765e-05 | 0.00288756 | missense, stop-gained, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053103 | GAGAACAGAACTTCA[C/G/T]AAGTAATGTATTTGG | 23510 |
rs150434976 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049381 | AAGTAGAATCTTTAA[A/C]GTTGTTTTACAGATT | 23510 |
rs150489476 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054425 | ATCCTGCCATTCGTC[A/G]TATGTTTGTCGTGTG | 23510 |
rs150541005 | snp | A/G | 0.108755 | 0.206276 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051258 | ACTGGGATTACAGAC[A/G]TGAGCCACCGCGCCC | 23510 |
rs150876625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042350 | GGTAATTTTCCTATC[C/G]CTTCTTCCTATGGCC | 23510 |
rs151054891 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064138 | AGTCTGGGGACCCCC[C/T]GTGTCTCTGACCACC | 23510 |
rs151161708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039945 | AATTATTTTGAAATT[C/T]GTCCATGTTGTTGCA | 23510 |
rs151314504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035102 | CTCTCTAGGAGGTAG[C/T]TGCAGCCGGAGACCG | 23510 |
rs180733106 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059318 | CACTTAAAAAGAAAA[A/G]CATTTTTTAAAGAGA | 23510 |
rs180757906 | snp | G/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032012 | AGTGATCAGTCTGCC[G/T]CAACCTCACAAAGTG | 23510 |
rs180768482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050642 | CCCTCAAGCATTTAT[C/T]CTTTGTGATACAAAA | 23510 |
rs180771527 | snp | A/G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065252 | CCTCGCTGCAACCCA[A/G/T]TGACACCTGTATTGT | 23510 |
rs180903187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062330 | GAACTCTTGCTCCTC[A/G]CTTCTTCCCTGGCCT | 23510 |
rs180905543 | snp | C/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046444 | AGAACAGATCATGCG[C/T]ATAGGAGGTGCTCAA | 23510 |
rs181237141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035210 | AATCCCTGCAACTAT[A/G]ATCTTCCCTCCCTTG | 23510 |
rs181367509 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051267 | ACAGACATGAGCCAC[C/T]GCGCCCGACCTTTTT | 23510 |
rs181415962 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040419 | CCCTGGACAATTCTT[C/T]ATGATGATAAGCTTC | 23510 |
rs181420846 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065510 | CCCCAGGTCTGGGAC[A/G]CAGGTGATGCCAGCC | 23510 |
rs181437394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045385 | GTTTTCAGATCAACC[A/G]GTCTGACCAAAATTT | 23510 |
rs181437586 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061373 | CAGCATGCTGGGCAC[A/G/T]GTGGTTCACACCTGT | 23510 |
rs181497953 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032417 | TTCTGGAACTAGGGC[A/G]GCGGCAGCAGGGATG | 23510 |
rs181498259 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057652 | GCAACTTCTGCCTCC[A/G/T]GGGTTCAAGCAGTTC | 23510 |
rs181516582 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053893 | TTTTTTTGAGACAGA[A/G]TCTCACTCTCTCCCC | 23510 |
rs181575380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058659 | CAAAAATTAGCCAGG[C/T]TTAGCGGCAGGCGCC | 23510 |
rs181705795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035391 | CTTGTTGTCTCTCTT[A/G]AGCTGGTACCTGGAA | 23510 |
rs181850679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040507 | ACCTTGAATTGTAAA[C/G]AAATTCTGATTTCTC | 23510 |
rs182094230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033894 | AAGGGATGGCACGGC[C/T]ACGTGCCCCAAGCCC | 23510 |
rs182097207 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031620 | TCCGAGGCCTGCCTG[C/T]GTCTGGACAGGAAAC | 23510 |
rs182141487 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051769 | ATGTAACCACAGACA[A/G]TACAGTTATCAAACT | 23510 |
rs182228235 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046005 | TCCACGTTCTTCTGC[C/T]ATGGTTTCAGCCGGT | 23510 |
rs182347291 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050339 | CAATCTTGACTCACT[A/G]CAACCTCAGCCTCCT | 23510 |
rs182503158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062066 | TTTGTGTAGCACTTT[C/T]GAAAGTATGTTAAGA | 23510 |
rs182579630 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037091 | GGCTCACGCCTGAAA[C/T]CCCAGCACTTTGGGA | 23510 |
rs182667424 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040661 | GAGGCTGAGGCGGGC[A/G]GATCACCTAAGGTCG | 23510 |
rs182827851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041844 | TCTTCACCAAGTTCA[A/G]CATCAATATGGTGAC | 23510 |
rs182860152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055430 | TCAAAGTTTTCTGGC[C/T]CTAGGCCAGGTATGG | 23510 |
rs182920132 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062498 | CCAAATCAATGAAAA[A/G]GAAAAGCTGGTTGCC | 23510 |
rs182921567 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047091 | TCCCGGGGGCGGGCA[C/T]AGCGCCTCCCCCGCG | 23510 |
rs183053657 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043623 | TCTCAAAAAAAAAAA[A/C]AAAAACAAACCCCAG | 23510 |
rs183056674 | snp | C/T | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060092 | TCCCCTACTTCTCTC[C/T]GCCTCGTGCTTACGA | 23510 |
rs183172702 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052595 | AGGCGTGGTGGCAAG[C/T]GCCTGTAATCCCAGC | 23510 |
rs183368449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056159 | AGAAGGGCTTATTCA[C/T]TTAGTTTTCTTCCAT | 23510 |
rs183388178 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036397 | AAGTGTTGTGATTAC[A/G/T]GGCGTGAGCCACCGC | 23510 |
rs183435568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054873 | TCTTTCATGCGATTA[A/G]ACTGTTTTAAGAAAC | 23510 |
rs183439044 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065826 | TGTTTGTGTGTTTGA[A/G]TAGTCTGAAATGCTG | 23510 |
rs183456120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059710 | CACGGGAGACGGCTA[C/T]GGCCAGGTGGGATCC | 23510 |
rs183458516 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034428 | GAGCACAGCCCCTCT[A/C]GACACCCCAGGTGGG | 23510 |
rs183598972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037707 | GACGTTGCTCAGGTC[G/T]GCTAACCATAGTAAA | 23510 |
rs183638927 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030642 | TGCAGTCGTCTCAGG[C/G]TAGCATTGCAGTAGT | 23510 |
rs183688267 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048796 | TTTTCTTGGAATTAG[A/G]AATGCAGTTCAGAGG | 23510 |
rs183692307 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063937 | CCTTTGATGGCTTGG[A/C]GTGGGGAAGGCTGTT | 23510 |
rs183694881 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035131 | CGCGTGGCCTAATGG[A/C/G]TAAGGCGTCTGACTT | 23510 |
rs183706331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052777 | TATGTGCCTGTAGTC[C/T]CAGCTACTTGGGAGA | 23510 |
rs183720628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051478 | TTGGTAGAGACGGGG[A/G]TTTCACCATGTTGGT | 23510 |
rs183833894 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75061127 | ATCTTATTACTGTCC[C/T]GTGGGAAGACGGAGG | 23510 |
rs184086698 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048066 | CCACAGCTGCAGGAA[A/G]CGCTCCTTGTGATAT | 23510 |
rs184136763 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045135 | ACGTTGGTAGGATCC[A/G]TGATGCCCCACAAGC | 23510 |
rs184195036 | snp | A/C | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045951 | AATTACAAAAGTATT[A/C]ATTTGGGGAACTAAT | 23510 |
rs184199714 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063481 | AATGGACGTTAGCAG[A/C]TGCTTCGGAACACCG | 23510 |
rs184259190 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049547 | GGTGAGAAGGAAGAT[A/G]GGTAGCTCCGCTTTG | 23510 |
rs184267139 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064118 | TATGTATGTATGTGC[C/T]AGGCAGTCTGGGGAC | 23510 |
rs184385005 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061413 | ACTTTGGGAGGCCAC[A/G]GTGGGAGGATTGCTT | 23510 |
rs184387736 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045447 | CTGGGATCGCTATGG[C/G]AGACTGGAGTTTATT | 23510 |
rs184419767 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044641 | GCCACCGCGCCCGGC[C/G]TGCATTTTAAGAGGT | 23510 |
rs184443431 | snp | C/T | 0.0007297 | 0.0190871 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039982 | GACAAGTCATTCCTT[C/T]ATATGGCTGTTAACT | 23510 |
rs184574135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056779 | TCTTTATTTTTTTGT[G/T]TGTGGATTTTCAAAC | 23510 |
rs185043015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054933 | AGAGTCGTGCTCCAC[C/T]ATGACTACCTGTGTT | 23510 |
rs185066783 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039221 | TACCTCTTTCTCATA[C/T]TCTACAATCCTGGCC | 23510 |
rs185069551 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036719 | CACATCCCTGCGCTT[C/T]CACTTGGCTGTCGTC | 23510 |
rs185087843 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056293 | CTATCTTACCTTTAC[A/G]TGGTATCTTTCACTA | 23510 |
rs185108620 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030974 | GGCGTGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 23510 |
rs185254546 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035097 | TTGGCCTCTCTAGGA[A/C/G]GTAGCTGCAGCCGGA | 23510 |
rs185365835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052736 | TTCGGGCGGGGGGAA[A/G]AAATAGAAACAGCCG | 23510 |
rs185373763 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032129 | TCAGTGAATAAATAC[A/G]TGGTTAGTGGCACTG | 23510 |
rs185383725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050781 | AACACAGAGAACTCC[C/T]TATATCCCAGATTAA | 23510 |
rs185383928 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065331 | CACCCACCCCCTTTA[A/G]GAACCAGGCTGGTGT | 23510 |
rs185394464 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050364 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 23510 |
rs185511189 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046505 | TGCACCCGAGGAGCC[C/T]TGAACGCTCTATACG | 23510 |
rs185519445 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031636 | GTCTGGACAGGAAAC[C/T]TGTGATTGAGAGAAT | 23510 |
rs185527268 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064706 | GCTGTAAAGTGTTAG[A/T]TGAACTGCCGTCCTC | 23510 |
rs185528978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062415 | TTAATTGGGATTTAC[A/G]GAGCACTGACAGGTG | 23510 |
rs185784219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040440 | GATAAGCTTCATTTT[C/G]TTCATCTGAAAAGGA | 23510 |
rs185937899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036105 | GTCACCCAGGGTGGA[A/G]TGCAGTAGCGTGATC | 23510 |
rs186068847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040656 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACCTAA | 23510 |
rs186071105 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058869 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT | 23510 |
rs186089870 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041247 | GTGGTCCCAGTTACT[C/T]GGGGGGATGAGGTGG | 23510 |
rs186200253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053352 | ATGGCGGGAGGAGGC[A/G]CCCAGGGCACTTTAG | 23510 |
rs186227744 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059350 | GGGAAAAAAAGAAAC[A/G]CCACAGTACTATTTG | 23510 |
rs186699924 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065522 | GACGCAGGTGATGCC[A/G]GCCAGGCCCAGGAGT | 23510 |
rs186733126 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057812 | ATGATCCGCCCACCT[C/T]GGTCTCCCAAAGTGC | 23510 |
rs186733455 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033021 | TGCGATGCTGGGGCA[G/T]ATTGGCAAGGTCCCA | 23510 |
rs186743576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051888 | CCTATAGGATCACAC[A/G]TCTCATAGTTGCCCT | 23510 |
rs186775440 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034002 | AGTTCCTTTTACGGA[A/T]TTTTTTATTTCTTTT | 23510 |
rs186878988 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048865 | TCAGTTACACAGCTA[C/G]GGCATTTTCTCCCTT | 23510 |
rs186879104 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063957 | GGAAGGCTGTTTCTT[C/T]GAAAGTTGCCAAATG | 23510 |
rs186911725 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030864 | GCACTTTGGGAGGCT[G/T]AGGCAGGCAGATCAC | 23510 |
rs186967097 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051270 | GACATGAGCCACCGC[G/T]CCCGACCTTTTTTTT | 23510 |
rs186998428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051585 | CACCATGCCCGACCT[C/T]TTTTTTTTTTAAATC | 23510 |
rs187102973 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054087 | CAGTGGCGTGATCAC[A/G]GCTCACTGCAGCCTT | 23510 |
rs187259845 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066035 | CTGCTACTGAAACCA[C/T]CAAAGGGGGTGTTGG | 23510 |
rs187491227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060039 | GAACAGCTGTGCTAG[A/G]AAGGATCAGGCGCCA | 23510 |
rs187601639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038103 | ATGCAAAAAGCTGTA[A/G]GTTAACTGTGCAACA | 23510 |
rs187606559 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062603 | TTTTCACTGCCTCAG[A/G]AGAAAAGGGTGTTTT | 23510 |
rs187612445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056246 | TTGCAGATTACCACT[C/T]GGAATGTGATCCAGT | 23510 |
rs187690080 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045089 | ACAAAAGAGAGAAAT[G/T]TTAAAGCTGGGCGTC | 23510 |
rs187790917 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060170 | CTCCATTAGATGGCA[G/T]ACTTGTTAAATTCTG | 23510 |
rs187791223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043694 | AAAATAACACTCTTA[C/T]TGCATAAAAGTTAAT | 23510 |
rs187833607 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048280 | CTAACCAAAGGGTTG[A/G]GAGGTGACAAGACAC | 23510 |
rs187866186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055569 | CCGGGCGTGGTGGCT[C/T]ATGCCTGTAATCCCA | 23510 |
rs188012535 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034436 | CCCCTCTCGACACCC[A/C]AGGTGGGACTCGAAC | 23510 |
rs188042117 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060743 | ACCGCCTGAGTAAAT[A/G]TGATTTTATACGGAT | 23510 |
rs188146401 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037147 | CAGGAGATCGAGACC[A/G]TCCTGCCTAACACGA | 23510 |
rs188297186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052654 | CTTGAACCCAGCAGG[C/T]GGAGTTTGCAGTGAG | 23510 |
rs188459486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035168 | AGAAGATTGAGGGTT[C/T]GAGTCCCTTCGTGGT | 23510 |
rs188468171 | snp | A/G | 0.00821588 | 0.0635645 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053128 | ATTTGGAACTGTTAA[A/G]GAGGGTTGTTTCAAG | 23510 |
rs188524423 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047768 | TCCCACTCCCCTTCT[C/T]CCATGCTGAGGCATA | 23510 |
rs188555645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061297 | GAGCTGCTCCCCTGC[C/G]TGTGTATTTCCTCTT | 23510 |
rs188584464 | snp | A/T | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065445 | ACCAGTGACCCACAC[A/T]CTCTGCTGCCCAGTA | 23510 |
rs188587459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045374 | CAGGAGACAGGGTTT[A/T]CAGATCAACCGGTCT | 23510 |
rs188800996 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063489 | TTAGCAGCTGCTTCG[G/T]AACACCGTCCCTCCT | 23510 |
rs188878286 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033712 | GCGTCCCAGTGCCGG[A/G]GGCTGGGGGCTGGTG | 23510 |
rs189085293 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057961 | GCACTTTGGGAGGCC[C/T]AGGTGGGTGGATCGC | 23510 |
rs189123963 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040470 | ACAGCTGGACTTGAT[A/G]ACCAAAAAATGGCCT | 23510 |
rs189331088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035098 | TGGCCTCTCTAGGAG[A/G]TAGCTGCAGCCGGAG | 23510 |
rs189335010 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052747 | GGAAAAAATAGAAAC[A/C]GCCGGGTGTGGTGGT | 23510 |
rs189474495 | snp | G/T | 0.0123036 | 0.0774623 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031832 | TGCAATGGCGCAATC[G/T]CGGGTCACTGCAACC | 23510 |
rs189496805 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039597 | AGCACCTAGCCAGAC[C/T]TCTCTCTGGTGGAGC | 23510 |
rs189499994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056957 | TTTCTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTG | 23510 |
rs189512372 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056467 | CATTCTCCCTTCTTC[A/G]TCATTAGCTAATTCC | 23510 |
rs189554922 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055252 | TAGAGATGGTGTTTC[A/G]CCATATTGACCAGGC | 23510 |
rs189594191 | snp | A/C/G | | | splice-acceptor-variant | KCTD2 | GRCh38.p7 | 17:75035231 | CCCTCCCTTGTTTTA[A/C/G]ACCCAGAAACGCCTC | 23510 |
rs189719024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040267 | AGGGCTGGAAGCTAC[A/G]AATCCTTAAAGGTCA | 23510 |
rs189864309 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053474 | GAGATGGAGTCTCGC[C/T]CTGTCGCCCAGGCCG | 23510 |
rs190162791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050235 | TTTTTCTTTTTTAAT[G/T]TTTGTAAGTACCTAG | 23510 |
rs190171765 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032413 | CACGTTCTGGAACTA[A/G]GGCGGCGGCAGCAGG | 23510 |
rs190193573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050911 | TCAAATGTCTGGCCT[C/T]ACATGCTCCTCCTGC | 23510 |
rs190328659 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061546 | TCCCAGCTACTCAGG[A/G]GGCTGACGTGGGAGG | 23510 |
rs190340264 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046912 | CGGATCCAATGCCCC[A/C]AGCCCCACTCACCTT | 23510 |
rs190340407 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062448 | TTTAGTTAGAAAATA[A/T]GAACCTAAAAAGGGT | 23510 |
rs190354294 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031200 | TCAAGGGACTCAGAG[A/C]CTAGGAGGGGGCTGA | 23510 |
rs190411823 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064735 | TCAGTAAAAGCAGCC[A/G]CCCCTTCAAGAGTCA | 23510 |
rs190427158 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064202 | GTGCCATGCTGGCGA[A/G]GATCCGGATGCGGCA | 23510 |
rs190471145 | snp | A/C | | | splice-acceptor-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042278 | GGTAAAGCAGCCAAC[A/C]TGCCCACAAGGAAAG | 23510 |
rs190489661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060080 | GGTGCGGCCGTTTCC[C/T]CTACTTCTCTCCGCC | 23510 |
rs190571504 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045985 | TGTCCATAAAATCTT[A/C]ACAATCCACGTTCTT | 23510 |
rs190642844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050552 | ACAGGCCTGAGCCTC[C/T]GCGCCCGACCTGAGA | 23510 |
rs190797270 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054142 | CCTACCTCAGCCTAC[C/T]GAGTAGCTGGGACTA | 23510 |
rs190831396 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036355 | CTCAATTTCCTGACC[C/T]AGTGATCCGCTCACC | 23510 |
rs190934148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046443 | TAGAACAGATCATGC[A/G]CATAGGAGGTGCTCA | 23510 |
rs190944653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051725 | CCTTAATATTTGTAT[A/G]TATTTCCCAAGAACA | 23510 |
rs190972991 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059195 | AAGTTTGTTGGCATA[C/G]TTGCTCAAGCATTCA | 23510 |
rs190989301 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033890 | GGGGAAGGGATGGCA[C/G/T]GGCCACGTGCCCCAA | 23510 |
rs191095843 | snp | A/G | 0.000407484 | 0.014268 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059641 | GCAATCCCAGGCCCC[A/G]TTCAAGGGGTCTGCA | 23510 |
rs191128467 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048402 | CACACCATCTTATAT[A/C]CCATATAGCACTCAG | 23510 |
rs191189607 | snp | A/G | 0.000131978 | 0.0081223 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062242 | GCCGAGCGAAAAGGC[A/G]AAGGTAAGGAGCCCC | 23510 |
rs191193797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036791 | AGTGACTGCAGTCTC[A/G]CAGGGGAAGGGTGTG | 23510 |
rs191324240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041711 | AAAAGGAACCCAGGA[C/G]GTGGGCAAACATTTA | 23510 |
rs191595814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034183 | GGGCCCCACAATTTC[A/G]AAGCTGGGGAAACTC | 23510 |
rs191654751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052035 | CCACCCCCAGTCCTT[C/T]TGAGGGCAGATTGGA | 23510 |
rs191655202 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065815 | CCCTCTGTTCCTGTT[C/G/T]GTGTGTTTGAATAGT | 23510 |
rs191749429 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030900 | CAGGAGATCGAGACC[A/G]TCCTGGCTAACATGG | 23510 |
rs191759446 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051459 | CTGGCTAATTTTTTT[A/G]TTTTTGGTAGAGACG | 23510 |
rs191820296 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064110 | CCCAGTGGTATGTAT[A/G]TATGTGCTAGGCAGT | 23510 |
rs191822744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049513 | AAGGAAGCCTCCTTA[G/T]GCTTTGTTCAGCTTC | 23510 |
rs191948551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062859 | GCAAGAGAGTGTTTC[A/G]CACCAGAAGCACTGC | 23510 |
rs192030908 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040659 | GGGAGGCTGAGGCGG[A/G]CGGATCACCTAAGGT | 23510 |
rs192038673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033113 | ATGTGAGTAGACTTT[C/T]ATTTAATAATTTTTT | 23510 |
rs192155774 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056515 | TTTCTGTTTGATGAC[C/T]GCAATTAAATTAATT | 23510 |
rs192209354 | snp | A/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047922 | TGAGATCTGCATGAG[A/T]TTTCCCTGGCTCCTC | 23510 |
rs192501879 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038643 | CAATTCTTTACTACA[C/T]CACAGTGAAATACAC | 23510 |
rs192509397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056280 | ACCAGTCTCTTTGCT[A/G]TCTTACCTTTACGTG | 23510 |
rs192527574 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063854 | TGCAGCCTCTTCTTA[C/G]TCCCCATTGACCCTG | 23510 |
rs192537098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039671 | TTAGGTATTTGAATA[C/T]TACTTGGGTAATTTT | 23510 |
rs192614699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035114 | TAGCTGCAGCCGGAG[A/G]CCGCGTGGCCTAATG | 23510 |
rs192627026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052765 | CGGGTGTGGTGGTAT[A/G]TGCCTGTAGTCCCAG | 23510 |
rs192668173 | snp | G/T | | | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060852 | CTTTGCATTAATGCT[G/T]TTATCTCACAGATCA | 23510 |
rs192735013 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037587 | TTGTAGGCATAACAG[G/T]TCCTCTGACTTTAAG | 23510 |
rs192807871 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052735 | TTTCGGGCGGGGGGA[A/T]AAAATAGAAACAGCC | 23510 |
rs192908003 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045106 | TAAAGCTGGGCGTCC[A/G]GGGGAGACATCACAC | 23510 |
rs192946789 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055890 | ACGAAAATTGTCTGA[A/G]TGTGGTAGCGGGCGC | 23510 |
rs193016229 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034937 | AATTCCCAGGGAGGC[A/T]CAGAGACTAGTCCAG | 23510 |
rs193285700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060182 | GCAGACTTGTTAAAT[G/T]CTGTTGCCTTCAAAA | 23510 |
rs199608192 | in-del | -/GACA | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063814 | GCACTGAGTCAGACA[-/GACA]AGTGGGAGCTGTAGG | 23510 |
rs199693457 | snp | A/G/T | 0.000214164 | 0.010346 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039185 | GAACCCATATTATAG[A/G/T]CAACGGCTACCCATC | 23510 |
rs199722316 | snp | A/G | 0.000857951 | 0.0206939 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062249 | GAAAAGGCGAAGGTA[A/G]GGAGCCCCTTCCCTG | 23510 |
rs199763854 | snp | C/T | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039261 | GACACCCACTCAGCA[C/T]AAGATTTCACCTTTA | 23510 |
rs199996653 | in-del | -/AAAATAAAAC | 0.0193772 | 0.0965046 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031120 | AAAATAAAATAAAAT[-/AAAATAAAAC]AAAATTGGAATGATA | 23510 |
rs200022144 | snp | A/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062135 | CTCATCAGCATCGGA[A/T]CTTCCTATAACTACG | 23510 |
rs200078977 | snp | C/G/T | 3.33757e-05 | 0.00408497 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042686 | GTCAAATAAAAACAA[C/G/T]GCTTTTTTATGAGGT | 23510 |
rs200237013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059640 | AGCAATCCCAGGCCC[C/T]GTTCAAGGGGTCTGC | 23510 |
rs200245940 | in-del | -/GT | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055372 | AGTTTACTTTTAAAA[-/GT]AAAAAATAATGCCTT | 23510 |
rs200278221 | in-del | -/A | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054810 | GGGAGACTCCATCTC[-/A]AAAAAAAAAAAAAGA | 23510 |
rs200283373 | snp | A/G | 3.30994e-05 | 0.004068 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042276 | CAGGTAAAGCAGCCA[A/G]CCTGCCCACAAGGAA | 23510 |
rs200307252 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058336 | TCTCAAAAAAAAAAA[A/G]GGAAAAAAAAATAAA | 23510 |
rs200410651 | snp | G/T | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042572 | TCAGGGAACTAGCAA[G/T]GGCCTTTTGGTTCTG | 23510 |
rs200412615 | snp | A/C | 3.2962e-05 | 0.00405954 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039113 | ACAGAGACGGAAAGC[A/C]GAATATCCAAGGCAG | 23510 |
rs200446567 | snp | A/G | 3.30874e-05 | 0.00406726 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062268 | GCCCCTTCCCTGGGC[A/G]GTTGCCTCTGGCTTG | 23510 |
rs200452841 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053858 | TGCTTGTGAACCATG[C/T]TTTTTTTTTTTTTTT | 23510 |
rs200538698 | in-del | -/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033131 | TAATAATTTTTTTTC[-/T]TTTTTTTTCTTTTTT | 23510 |
rs200610566 | in-del | -/CCCAACAC | 0.0766824 | 0.180169 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035568 | GCTCACGCCTGTAAT[-/CCCAACAC]TTTGGGAGGCTGAGG | 23510 |
rs200708577 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062016 | TAAAGAGTTAAACCT[C/T]TGATAACTTAAAAGT | 23510 |
rs200793762 | snp | C/G | 0.00199792 | 0.0315431 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042249 | AAGCCCAGTCGATAG[C/G]TGGTGGATTCTCAGG | 23510 |
rs200848025 | in-del | -/AT | 0.00953873 | 0.0683987 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044666 | AGAGGTATTCAACAC[-/AT]GTGAAAATGTGAGAA | 23510 |
rs200894845 | in-del | -/AGGAGATC | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030886 | GCAGATCACGTGGTC[-/AGGAGATC]GAGACCATCCTGGCT | 23510 |
rs201063763 | in-del | -/TC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057573 | TTTTTTTTTTTTTTT[-/TC]CTCGAGGCAGAGTCT | 23510 |
rs201343144 | snp | A/G | 5.05038e-05 | 0.00502487 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049335 | CAGAAGAAGGTAAGC[A/G]CACTGTTTGCATTGG | 23510 |
rs201421376 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056945 | TGTTTCTTTTTTTTT[C/T]TTTTTTCTTTTTTTT | 23510 |
rs201426255 | snp | C/T | 0.000741465 | 0.0192401 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059632 | AACAGAGCAGCAATC[C/T]CAGGCCCCGTTCAAG | 23510 |
rs201437197 | snp | A/C | 0.000381297 | 0.0138023 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042184 | GTGAAGTCTCACCTT[A/C]TTCTCAAAGTCATCC | 23510 |
rs201465890 | snp | A/G | 0.000247196 | 0.0111147 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039068 | ATCTTCTCCATCTGG[A/G]AAGAGGGGGAATGTG | 23510 |
rs201521579 | snp | A/C/G | 9.89942e-05 | 0.0070348 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039306 | TTCAGTTCTGAAACC[A/C/G]GGCTGCATTCTACCC | 23510 |
rs201650407 | in-del | -/G | 0.0766824 | 0.180169 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035576 | TGTAATCCCAACACT[-/G]TTGGGAGGCTGAGGC | 23510 |
rs201662153 | in-del | -/TG | 0.0162398 | 0.0886349 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064034 | AATGCCTTGACTGAA[-/TG]TGCAATATTTGTGTC | 23510 |
rs201751897 | in-del | -/CAGA | 0.00557542 | 0.0525036 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036242 | GAGTTTTGTCTGCAG[-/CAGA]CAAACAAGCTGGGGC | 23510 |
rs201766965 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058338 | TCAAAAAAAAAAAAG[A/G]AAAAAAAAATAAAAA | 23510 |
rs201853629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049177 | CCTTTGTTTAAAATA[C/T]TCCTCAAAGGTCCAC | 23510 |
rs201925883 | snp | C/G/T | 8.35742e-05 | 0.00646382 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062994 | CTCAGCAGCCTCAGC[C/G/T]TCTCCCCCATCTCCA | 23510 |
rs201992480 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037365 | AAAAAAAAAAAAAAA[C/T]AAATGGCAGAAATGT | 23510 |
rs202181641 | snp | A/G | 4.9445e-05 | 0.00497193 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053046 | GAGTTTTACAACATC[A/G]CGTCCCTTGTGCGGC | 23510 |
rs202190566 | in-del | -/AGC | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044505 | CACCGCGCCCGGCCC[-/AGC]TAATTTTTGTATTTT | 23510 |
rs202201681 | in-del | -/A | 0.0482946 | 0.147699 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045001 | CCCAAACATCAGTGT[-/A]ATCGGGGAACTTGCC | 23510 |
rs207476584 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033826 | GACCCACTCCATGGA[C/T]CGCGCCTCTGTCAGG | 23510 |
rs367762476 | snp | G/T | 1.65162e-05 | 0.00287365 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75049248 | CCTATCTGATTGACA[G/T]GGACCCCACCTACTT | 23510 |
rs367889953 | snp | A/G | 4.94401e-05 | 0.00497168 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040074 | ATTTTAGAATAAGCA[A/G]GAGCCTCAACTACTT | 23510 |
rs367969400 | snp | A/T | | | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060771 | GATTATGCCTACTTA[A/T]GTGTAGAGTTTTAAC | 23510 |
rs367974157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055712 | TGGCACATGCCTGTA[A/T]TCCCAGCTACTTGGG | 23510 |
rs368122033 | snp | C/G/T | 4.94461e-05 | 0.00497202 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052976 | TTTTTCTGGCAAACC[C/G/T]TCGCACCTATCTGAC | 23510 |
rs368173464 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058227 | TATTCAAGAGGCTGC[C/T]GAAGCAGGAGAATCG | 23510 |
rs368359569 | snp | C/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040644 | TAATCCCAGCACTTT[C/G]GGAGGCTGAGGCGGG | 23510 |
rs368389022 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063598 | GAGTTGCCAGAGTAC[C/T]CCGCATTCCCATGAA | 23510 |
rs368559600 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055829 | AGGAGCGAAACTCCC[A/C]TCTAAAAAAAAAAAA | 23510 |
rs368570853 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062207 | GAACTAAATAATTCT[A/G]CCAATGGCATCGTCA | 23510 |
rs368577983 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066325 | GCTGGGATTACAGGC[A/G]CCTGCCTGCGCGCCT | 23510 |
rs368636603 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040864 | GCACTCCAGCCTGGG[A/C]GACAGAGCAAGACTC | 23510 |
rs368706584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062936 | ACCATCATGCCACTC[A/G]TCGGGTCCAGTGGAA | 23510 |
rs368759395 | snp | A/G | 6.60513e-05 | 0.00574641 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059548 | AGTCCTGCAGTGTCA[A/G]GAAGAAGAGCTCACG | 23510 |
rs368812104 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035104 | CTCTAGGAGGTAGCT[A/G]CAGCCGGAGACCGCG | 23510 |
rs368830453 | in-del | -/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031784 | TTTGTTTGTTTTTTT[-/T]GAGACAGAGTCTCAC | 23510 |
rs368912962 | snp | C/T | 1.64746e-05 | 0.00287002 | stop-gained, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039251 | CTTTGAGAGAGACAC[C/T]CACTCAGCACAAGAT | 23510 |
rs368992316 | snp | A/C | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046418 | AATCTATTGCTTAAT[A/C]CCCAGCGCCTAGAAC | 23510 |
rs369048557 | snp | A/G | | | intron-variant, synonymous-codon | KCTD2 | GRCh38.p7 | 17:75059974 | CTTTTCCCAGGGTCA[A/G]AACTTTTTGGTTCTG | 23510 |
rs369092564 | snp | C/T | 5.07224e-05 | 0.00503573 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059637 | AGCAGCAATCCCAGG[C/T]CCCGTTCAAGGGGTC | 23510 |
rs369140526 | snp | A/G | 0.000615811 | 0.0175364 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063059 | GTAAACTAAGACCCC[A/G]AAAACTCCAGACCTT | 23510 |
rs369174610 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051094 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 23510 |
rs369201003 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037715 | TCAGGTCTGCTAACC[A/G]TAGTAAATAGTGGGG | 23510 |
rs369247930 | snp | A/G | 1.65023e-05 | 0.00287244 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059566 | AGAAGAGCTCACGCA[A/G]ATGGTGTCCACGATG | 23510 |
rs369287155 | snp | G/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045438 | CTAATAAGCCTGGGA[G/T]CGCTATGGGAGACTG | 23510 |
rs369373095 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062699 | ACCCCCCTCACCCCC[A/C]ACACACACACACACA | 23510 |
rs369383925 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041100 | ATGGTGGCTCACACC[C/T]GTACTCCCAGCACTT | 23510 |
rs369432437 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046628 | CCCAGTCCCCCCACC[A/G]AACTATTGAAGTCTG | 23510 |
rs369483244 | snp | C/T | 0.000329614 | 0.0128335 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040181 | ACAAACACAAGGGCA[C/T]GGGAACCTTCAGCGC | 23510 |
rs369589395 | snp | C/T | 1.69252e-05 | 0.00290901 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042148 | CCCACAGGCATGTTA[C/T]AAGCTCAGTGCTTTA | 23510 |
rs369669167 | snp | A/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047080 | CGGAAGTATCTTCCC[A/G]GGGGCGGGCACAGCG | 23510 |
rs369681620 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052306 | TAATGCAGTTTTTAG[G/T]CCAGGAGCTGTGGCT | 23510 |
rs369697131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056493 | ATTCCTGGAGAGCAT[C/T]ATAAGATTTCTGTTT | 23510 |
rs369878069 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051564 | GCTGCGATTACAGGC[A/G]TGAGCCACCATGCCC | 23510 |
rs370039094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049557 | AAGATAGGTAGCTCC[A/G]CTTTGCAGATAACTT | 23510 |
rs370063205 | snp | G/T | 1.64749e-05 | 0.00287005 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062077 | CTTTCGAAAGTATGT[G/T]AAGATTGCCACATGA | 23510 |
rs370259773 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064214 | CGAGGATCCGGATGC[A/G]GCAGCACCCTCTTTC | 23510 |
rs370351086 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061461 | GACCAGCCTGGGCAA[C/T]ATAGCGAGACCCCCC | 23510 |
rs370502067 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052975 | GTTTTTCTGGCAAAC[C/T]CTCGCACCTATCTGA | 23510 |
rs370683979 | snp | A/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048791 | AGAGGTTTTCTTGGA[A/G]TTAGGAATGCAGTTC | 23510 |
rs370778824 | snp | A/G | 4.9423e-05 | 0.00497082 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062115 | CTGTATTCTTGGTTC[A/G]TCAGCTCATCAGCAT | 23510 |
rs370823634 | snp | G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044131 | CCAGGCTCAAGCGAT[G/T]CTCCTGCCTCAGCCT | 23510 |
rs370834832 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057017 | TGGAGTGCAGTGATG[C/T]GATCTCAGCTCACTG | 23510 |
rs370862858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035788 | CAGTGAGCCGTGATC[A/G]CGCCACTGCACTCCA | 23510 |
rs370939707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057976 | TAGGTGGGTGGATCG[C/T]CTCAGGTCAAGACCA | 23510 |
rs371049238 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035188 | CCCTTCGTGGTCGGA[A/C]CGTTTTAATCCCTGC | 23510 |
rs371078821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057937 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 23510 |
rs371155959 | snp | C/G/T | 9.88507e-05 | 0.00702969 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039189 | CCATATTATAGGCAA[C/G/T]GGCTACCCATCATCC | 23510 |
rs371294671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039345 | GCTAAGGTAGGAGTC[A/G]TCCCAGCCCACTCCT | 23510 |
rs371474881 | snp | A/G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040374 | GAACAGGAGCTCAAG[A/G/T]GTCTTCTCAGCCCTA | 23510 |
rs371496915 | snp | C/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031484 | GTGACTAGTTCTAGC[C/T]GGAGGGTTGGAGAAG | 23510 |
rs371500387 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054028 | CTTGATTTTGGCGGG[A/G]AGAGGGAGGACAAGG | 23510 |
rs371524705 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042327 | CATAAGCAGTAGAAA[A/T]TTCACATGGTAATTT | 23510 |
rs371625622 | snp | A/C/G | 0.000148272 | 0.00860906 | intron-variant, missense | ATP5H, KCTD2 | GRCh38.p7 | 17:75040153 | GGCACGGGAACCTTC[A/C/G]GCGCATTAAACTACA | 23510 |
rs371683212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036827 | TCTGTTACGCACATT[A/G]AAGGCCTTGCACAGC | 23510 |
rs371743636 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033976 | CGAGTCCCACCTGGG[A/G]TAGAGGTGAAAGTTC | 23510 |
rs371749352 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058783 | AGCCTGGGCGACAGA[A/G]TGAGACTGTGTCTTA | 23510 |
rs371810467 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051595 | GACCTTTTTTTTTTT[A/T]AAATCATATTTGCAT | 23510 |
rs371897572 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036589 | AATCTCCCAAAGGGC[C/T]CCCCCTAATGCTGGG | 23510 |
rs371967820 | in-del | -/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062690 | CCACTGTGCACCCCC[-/C]TCACCCCCAACACAC | 23510 |
rs372068938 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75050527 | CTCAGCCTCCCAGAG[G/T]GCTGGGATTACAGGC | 23510 |
rs372096724 | snp | A/G | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062234 | GTCATAGAGCCGAGC[A/G]AAAAGGCGAAGGTAA | 23510 |
rs372119032 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059243 | ATTATTTTACCTTTT[G/T]TATTCTTTCACTCTT | 23510 |
rs372152326 | snp | C/G | 0.000875616 | 0.0209055 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039327 | CATTCTACCCCAGCA[C/G]CTGCTAAGGTAGGAG | 23510 |
rs372458611 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047808 | TCTCCCCGACCCCGC[C/T]CTTCGTTCTCTGAGA | 23510 |
rs372510854 | snp | C/G | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046582 | CAGCTGAGCGTCCCT[C/G]GGCAGGTTAACACTG | 23510 |
rs372560759 | in-del | -/TCTGGCTCC | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041959 | CTGATCAGAAAGCCC[-/TCTGGCTCC]CAGATTAAGGCTACA | 23510 |
rs372630398 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062962 | TGGAAAGCATCCCCC[A/G]ACATCTCTGTCTTTC | 23510 |
rs372683545 | snp | C/G/T | 3.29925e-05 | 0.00406145 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038975 | CAATAGGGATACTTT[C/G/T]TCTTGTCTAATTTGG | 23510 |
rs372908703 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041116 | GTACTCCCAGCACTT[C/T]GGGAGGCCAAGGAGG | 23510 |
rs372915829 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059835 | TTCACACGCAGACTT[A/T]CCAGGGGAGCCAACG | 23510 |
rs373074471 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037685 | CTTTAAACCATCTCT[A/G]TTGCCTGACGTTGCT | 23510 |
rs373196222 | snp | G/T | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046114 | GTGAGACGGAGTCTC[G/T]CACTGTCGCCTGGGC | 23510 |
rs373265198 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033836 | ATGGATCGCGCCTCT[C/G]TCAGGCCTTCTCTAG | 23510 |
rs373289529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060631 | GGTTCATGGCTGGGC[A/G]CGTGGCGAGTGGGCC | 23510 |
rs373370441 | snp | A/G | 1.6504e-05 | 0.00287258 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059563 | GGAAGAAGAGCTCAC[A/G]CAGATGGTGTCCACG | 23510 |
rs373376357 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75046935 | CTCACCTTCACCGAC[C/T]CTGGCTGCCCACGGT | 23510 |
rs373438974 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061971 | GGCCCATTTCTCCCC[A/G]GGGGCTTTGGTAGTC | 23510 |
rs373448090 | snp | A/T | | | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75035245 | AGACCCAGAAACGCC[A/T]CCCAATCCCTCCACA | 23510 |
rs373473558 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057634 | GCGCGATCTCAGCTC[A/G]CTGCAACTTCTGCCT | 23510 |
rs373552679 | snp | A/C/G | 0.000115709 | 0.00760549 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042494 | TTTCTAGATTCAGTG[A/C/G]CAAGTATGGGGTTCC | 23510 |
rs373588497 | snp | A/G | 3.29652e-05 | 0.00405974 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040182 | CAAACACAAGGGCAC[A/G]GGAACCTTCAGCGCA | 23510 |
rs373687971 | in-del | -/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056193 | GCTGACAGCTCAAAG[-/G]CTCCTTTTTGATGTT | 23510 |
rs373721085 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034724 | TGTAACCCCGAGAAG[A/T]AGTGCTCGGCGAGCG | 23510 |
rs373722327 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053510 | CAGTGGTGCAATCTC[A/C/G]GCTCACTGCAACCTC | 23510 |
rs373746141 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056692 | AAGACACCCTCTTTT[A/G]TACTTGTTGTATGTG | 23510 |
rs373843432 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065695 | TGTCAGTGAGGCTGG[A/G]AGCAGGGAGCCACGG | 23510 |
rs373965692 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064818 | AAGGAAAGTAGTGAT[C/T]ACGGGAAGGACTGCT | 23510 |
rs373969865 | snp | G/T | | | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038814 | AGTGAGGCCAGCTCA[G/T]AAGAGAGGCTTAATT | 23510 |
rs373972881 | snp | A/G | 5.20215e-05 | 0.00509981 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049360 | CATTGGGGATTTTCA[A/G]AATGCAAGTAGAATC | 23510 |
rs374058787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055703 | CTGGGGTGGTGGCAC[A/G]TGCCTGTAATCCCAG | 23510 |
rs374082156 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063696 | TGGATTTGGGGCTCC[C/T]GGCTGCCACCACATG | 23510 |
rs374144823 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75062150 | TCTTCCTATAACTAC[A/G]GCAATGAGGATCAGG | 23510 |
rs374250140 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065103 | GGCGCCGTTTCCTTC[A/G]TTCCTCTTAGATTCC | 23510 |
rs374255791 | in-del | -/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056952 | TTTTTTTTCTTTTTT[-/C]TTTTTTTTTTTTTTT | 23510 |
rs374311158 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063216 | CTCCCTCCCCACCTG[C/T]AGGACTCCGAAGACA | 23510 |
rs374316148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051933 | CATTTAGCATGCAAG[A/T]CTTTAAATGGTTGCC | 23510 |
rs374481275 | snp | A/G/T | 1.65985e-05 | 0.00288079 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040044 | CTATAATAGAGAGCT[A/G/T]TCAAGATCAAGAGAA | 23510 |
rs374613354 | snp | A/G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066297 | AAGCAATTCTCCCTC[A/G/T]GCTTCCTGAGTAGCT | 23510 |
rs374655389 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036944 | TCAACCCGGCCTTAC[C/T]CCTACCAATCAGGAG | 23510 |
rs374828075 | snp | A/T | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048902 | TAACAAACACGCTAC[A/T]GAAGAATGTTTGTCA | 23510 |
rs374861835 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037825 | GAGGCTGAGGCGGGC[A/G]GATCACAAGGTCAGG | 23510 |
rs374880067 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041157 | TGAGCTCAGGAGTTC[A/G]AGACCAGTCTGGGCA | 23510 |
rs374882994 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059946 | CTGGGATTCGACAAC[A/C]ATCCTTCCATTTCTT | 23510 |
rs374909339 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75061851 | GCGTGGGCATGTTAA[G/T]CCTGCCGCTGACGGG | 23510 |
rs374916514 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036680 | CGAGCTCTAACTATG[C/G]TCCAAGTAAACTGCA | 23510 |
rs374931458 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75056952 | TTTTTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 23510 |
rs375036346 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036672 | GAACAGCGCGAGCTC[C/T]AACTATGCTCCAAGT | 23510 |
rs375086864 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035938 | CTAGTGGGCTCTGTC[C/T]ACACTCACACGGCAC | 23510 |
rs375114115 | snp | C/T | 3.29592e-05 | 0.00405938 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040173 | ATTAAACTACAAACA[C/T]AAGGGCACGGGAACC | 23510 |
rs375122828 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75058066 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 23510 |
rs375158100 | snp | C/G | 3.76783e-05 | 0.00434024 | upstream-variant-2KB, missense, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047563 | CGCCTCTGCTGCCAG[C/G]AGGACCCGGAGCTGG | 23510 |
rs375187567 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75055828 | CAGGAGCGAAACTCC[C/G]ATCTAAAAAAAAAAA | 23510 |
rs375346302 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063439 | TTGTTCCCGTGCCGT[A/G]CCATGGTTTCACCCT | 23510 |
rs375365983 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042289 | CAACCTGCCCACAAG[A/G]AAAGGCAAAAGTTAG | 23510 |
rs375367412 | snp | C/G | 4.9802e-05 | 0.00498984 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042285 | CAGCCAACCTGCCCA[C/G]AAGGAAAGGCAAAAG | 23510 |
rs375369794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060817 | TCACCAGATGCTTAC[C/T]TTCTAAAAGAAAACT | 23510 |
rs375395740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054744 | CCCAGGAGGCGGAGC[A/T]TGTAGTGAGCCAAGA | 23510 |
rs375854712 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064466 | TGTGTGCTCCACAGC[G/T]CACCTGCTTGCCAAG | 23510 |
rs376029867 | in-del | -/TTTCTT | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039902 | TGCTATACTCTTCTT[-/TTTCTT]GTTGGCTTCTTTCAC | 23510 |
rs376097927 | snp | C/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037689 | AAACCATCTCTATTG[C/G]CTGACGTTGCTCAGG | 23510 |
rs376239291 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048238 | TGAAAATTTTCCCGG[A/G]AAAATTTTGGGCAGG | 23510 |
rs376423661 | in-del | -/TCTTTTCTT | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033147 | TTTTTTTCTTTTTTT[-/TCTTTTCTT]CAAATGAGACTGCAT | 23510 |
rs376457589 | snp | G/T | 4.95618e-05 | 0.00497779 | missense, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059544 | ACAGAGTCCTGCAGT[G/T]TCAGGAAGAAGAGCT | 23510 |
rs376513861 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059399 | GGCTGCCAAGAAAAG[A/G]TTTCCAAGCAAACTC | 23510 |
rs376526597 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034725 | GTAACCCCGAGAAGA[A/G]GTGCTCGGCGAGCGC | 23510 |
rs376529473 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75053665 | TCAGGCTGGTCTCGA[A/T]CTCCCGACCTCAGGT | 23510 |
rs376551538 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036973 | AGCCATGCACCCAGG[C/T]TCTCCTCTGCTTATG | 23510 |
rs376593985 | snp | A/C | 3.29919e-05 | 0.00406138 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75053073 | CGGCTGGTTAAGGAA[A/C]GGATACGGGACAATG | 23510 |
rs376749903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052203 | CTGGCGTTTGACTAA[C/T]TTATGTTGGAGAAAA | 23510 |
rs376884901 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051441 | AGGTGCATGCCACCA[C/T]GCCTGGCTAATTTTT | 23510 |
rs376925615 | snp | A/T | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039063 | TCTTCATCTTCTCCA[A/T]CTGGAAAGAGGGGGA | 23510 |
rs376934365 | snp | A/G | 1.65999e-05 | 0.00288091 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042286 | AGCCAACCTGCCCAC[A/G]AGGAAAGGCAAAAGT | 23510 |
rs376976639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042932 | TTCAAGGTAATTCAA[C/G]GTGTGCGGCCAGGCG | 23510 |
rs377052083 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060437 | TCAAAAAGCCAAAAA[A/T]GTCCTCTAACATAAG | 23510 |
rs377072220 | snp | G/T | 1.70781e-05 | 0.00292212 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059650 | GGCCCCGTTCAAGGG[G/T]TCTGCAGCTCTTCAA | 23510 |
rs377237619 | snp | C/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047802 | TGGCTTTCTCCCCGA[C/G]CCCGCCCTTCGTTCT | 23510 |
rs377288112 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033779 | CGCGGTATCTTCCCG[C/T]CCGCTCACCAAAAGT | 23510 |
rs377338555 | snp | A/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048258 | TTTTGGGCAGGATGC[A/T]TGGCTGCTAACCAAA | 23510 |
rs377550721 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059611 | ATTCGAACAGGTACA[C/T]CTCTTAACAGAGCAG | 23510 |
rs377590780 | snp | A/G | 8.25294e-05 | 0.00642323 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042244 | GTAGTAAGCCCAGTC[A/G]ATAGCTGGTGGATTC | 23510 |
rs377594522 | snp | A/C | 1.6507e-05 | 0.00287284 | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042243 | TGTAGTAAGCCCAGT[A/C]GATAGCTGGTGGATT | 23510 |
rs377649941 | snp | A/G | 4.94271e-05 | 0.00497102 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039178 | AAAGAGAGAACCCAT[A/G]TTATAGGCAACGGCT | 23510 |
rs377651173 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041989 | AAGGCTACACTCTAC[C/T]GCTGAATGAACAGAG | 23510 |
rs377713724 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065128 | GATTCCATAGTTGCC[A/G]CCATGAAAAGACTGC | 23510 |
rs386386616 | in-del | -/AA | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041462 | AAAAAAAAAAAAAAA[-/AA]ACAAAACGAAAATTT | 23510 |
rs386799199 | multinucleotide-polymorphism | CT/TC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033130 | TTTAATAATTTTTTT[CT/TC]TTTTTTTTCTTTTTT | 23510 |
rs386799200 | in-del | CCCAACACT/TG | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035568 | GCTCACGCCTGTAAT[CCCAACACT/TG]TTGGGAGGCTGAGGC | 23510 |
rs386799201 | multinucleotide-polymorphism | AG/CA | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044960 | GATTTTAAAGTTACC[AG/CA]GGAACCAAGCACCCT | 23510 |
rs397725620 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031829 | GAGTGCAATGGCGCA[-/A]TCTCGGGTCACTGCA | 23510 |
rs398041900 | in-del | -/A | 0.5 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058347 | AAAAGGAAAAAAAAA[-/A]TAAAAAATTAGCTGG | 23510 |
rs527261874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046749 | GCGCCAAGGAGGGCT[A/G]AGGAAGGGATCGCGG | 23510 |
rs527262008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040230 | GGACAGTGAGTCGTC[A/G]CCAATACACCCAGGA | 23510 |
rs527311881 | snp | C/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040424 | GACAATTCTTTATGA[C/T]GATAAGCTTCATTTT | 23510 |
rs527317386 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052673 | GTTTGCAGTGAGCCA[A/C]GATCATGCCATTGCA | 23510 |
rs527328108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046295 | CACTACGTTGGCCAG[A/G]CTGGTCTCGAACTCC | 23510 |
rs527538115 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035083 | TAATGGCCATCAAAT[A/T]GGCCTCTCTAGGAGG | 23510 |
rs527801827 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75045144 | GGATCCGTGATGCCC[C/T]ACAAGCCACAAAAAC | 23510 |
rs527921230 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063432 | AAGAGGATTGTTCCC[A/G]TGCCGTGCCATGGTT | 23510 |
rs527923532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056879 | CCTCAACCCTACCTT[C/T]GGTTTCATGACCTCT | 23510 |
rs527946360 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065851 | ATGCTGTGACTTTTT[G/T]TGTGTGAATAAAGAT | 23510 |
rs527956708 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062886 | CTGCGGGTGAGGCTG[C/T]GGCTGCACCCCTGCT | 23510 |
rs528011992 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064230 | GCAGCACCCTCTTTC[G/T]GGCTGCATCCACAGA | 23510 |
rs528048074 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065783 | AGACTTAGGGACGAG[A/G]CTGTCACTGGTGGGC | 23510 |
rs528131138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036645 | TTCACGGGGCTCAGC[A/G]GTGCTCTCCTTGAAC | 23510 |
rs528225696 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75034504 | TTAGGCCACTGGGGC[A/G]CGGTAAGACGCTAAA | 23510 |
rs528316195 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060698 | CTGCACTCAGGGTCT[A/C]GGTCGCCGCCACTCG | 23510 |
rs528332994 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054680 | GGCATGGTGATGGGT[G/T]CCTGTAGTCCCAGCT | 23510 |
rs528354818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060354 | TCCACTGGAAAAATG[C/T]AGTCCTTGATATTTC | 23510 |
rs528418031 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052817 | GAGAATCATTTGAAC[A/G]CAGGAGGCGGAGGTT | 23510 |
rs528431195 | snp | A/G | 1.65097e-05 | 0.00287308 | synonymous-codon, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75059551 | CCTGCAGTGTCAGGA[A/G]GAAGAGCTCACGCAG | 23510 |
rs528564435 | snp | C/T | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060072 | GGAAGTGTGGTGCGG[C/T]CGTTTCCCCTACTTC | 23510 |
rs528575774 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064598 | ACCCTCAGTCTCCTT[A/C/G]TTTCTCTGTATCTGT | 23510 |
rs528609598 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030676 | TTGCTCTGGCATGTA[C/T]AAATTTCTTAAACTG | 23510 |
rs528642982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041961 | GATCAGAAAGCCCTC[C/T]GGCTCCCAGATTAAG | 23510 |
rs528800724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053598 | GGTGTGTGCCACCAC[A/G]CCTGACTAATTTTTG | 23510 |
rs528851201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056765 | TCATTTTGTATTTTT[C/T]TTTATTTTTTTGTGT | 23510 |
rs528979011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062056 | AGAGGGGTGATTTGT[A/G]TAGCACTTTCGAAAG | 23510 |
rs529052384 | snp | A/G | | | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038510 | AAGTAAATCCCTGCT[A/G]TTACACCTAGCCATT | 23510 |
rs529126364 | in-del | -/AAAG | 0.00318978 | 0.0398085 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055843 | CATCTAAAAAAAAAA[-/AAAG]AAAGAAAGAAACCCT | 23510 |
rs529129294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045214 | TATACGAATAGGTGT[A/G]GGTGACAGACATCAA | 23510 |
rs529155562 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044785 | AAAAGACTGCAAAGT[A/C]AAAAATCTCTATAAG | 23510 |
rs529207788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051515 | GGTCTTGAACTCCTG[A/C]CCTCGTGATCCACCC | 23510 |
rs529318474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050374 | TCAAGCGATTCTCCT[C/G]CCTCAGCCTCCCAAG | 23510 |
rs529387850 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049766 | TCTTTTAAGACTCTG[A/G]CCTCATGCTTCCCTG | 23510 |
rs529520107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033208 | TCCTGGGCTCAAGCA[A/G]TCCCCCCACCTCACC | 23510 |
rs529633747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038038 | TGGGCGACAGAGTGA[C/G]ACTCCATCTTAAAAA | 23510 |
rs529692809 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041248 | TGGTCCCAGTTACTC[A/G]GGGGGATGAGGTGGG | 23510 |
rs529693664 | snp | A/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75052512 | GGATCACCTGAGGTC[A/C]GGAGTTCAAGACCAG | 23510 |
rs529697491 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047630 | CCGGGCCTTCGAACC[C/T]CCTGGTTTCTCGTAG | 23510 |
rs529753822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050934 | CCTCCTGCCTCAGCC[G/T]CCTGAGTAGCTGCGA | 23510 |
rs529758048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040683 | CTAAGGTCGGGAGTT[C/T]GAGACCAGCCTGACC | 23510 |
rs529800439 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046881 | AGAGGGCAGAGCAGA[A/G]GAGCCCTCCAGGGAT | 23510 |
rs529824339 | snp | A/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065139 | TGCCGCCATGAAAAG[A/T]CTGCTCTTGAGCCCC | 23510 |
rs529909872 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064677 | GTCTACACACCTATG[C/T]GCCACATTTTACAGC | 23510 |
rs529955015 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030813 | TGCATACTAAAACTG[G/T]AATGCCAGGCACGGT | 23510 |
rs530010294 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063467 | CCTATGTGTGCCACA[A/G]TGGACGTTAGCAGCT | 23510 |
rs530089508 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034467 | CCACAATCCCTGGCT[G/T]AGGAGGCCAGTGCCT | 23510 |
rs530263451 | snp | C/G/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044695 | GAAAAATACAGAAAA[C/G/T]GACTACAGCCACTTA | 23510 |
rs530275487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058313 | GCCTGGGCGACAGAG[C/T]GAGACTCTCTCAAAA | 23510 |
rs530278775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052360 | GAAGGCCAAGGTGGG[C/T]GGATCACTTGAGGTT | 23510 |
rs530312146 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063992 | ATGTTGTGTCTCAGA[A/G]AGAGTTATTTCTGTG | 23510 |
rs530397707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060706 | AGGGTCTCGGTCGCC[A/G]CCACTCGCCACCCTG | 23510 |
rs530533722 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031937 | CAGCTAATTTTTGTA[C/T]TTTTAGTAGAGATGG | 23510 |
rs530536236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037397 | ACAAGTCTCCCCTGC[A/G]TAGACCATGCAGACT | 23510 |
rs530580124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050459 | GTAGAGACAGGGTTT[C/T]ACCATGTTGACCAGG | 23510 |
rs530593941 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055458 | TGGTGGCTCACGCCT[A/G]TAATCCCAGCACTCT | 23510 |
rs530666982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055600 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 23510 |
rs530783198 | snp | C/G | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049883 | TGGGACTATAAGTGG[C/G]TCTAGTCCACTTTCT | 23510 |
rs530818694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061146 | GGAAGACGGAGGGTG[C/T]TCCTATTGCCTCCCT | 23510 |
rs530899703 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048286 | AAAGGGTTGAGAGGT[A/G]ACAAGACACTTAAAC | 23510 |
rs530974857 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053735 | GGCGTGAGGCACTGC[A/G]CCCAGCTTGGCCACT | 23510 |
rs531006957 | in-del | -/G/GG | 0.0255113 | 0.110578 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061863 | AATCCTGCCGCTGAC[-/G/GG]GGGGGGGGACTTCAG | 23510 |
rs531046978 | in-del | -/T | 0.326035 | 0.238157 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057556 | TGATAGCTATACCTC[-/T]TTTTTTTTTTTTTTT | 23510 |
rs531131533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049015 | ACCTAAGATGATCTT[A/G]ATGTACAAGATACAT | 23510 |
rs531379710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034511 | ACTGGGGCGCGGTAA[A/G]ACGCTAAACCCACGT | 23510 |
rs531381006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040572 | AGGAGCACTGCGTAA[G/T]GAATGGTCTCCTTAG | 23510 |
rs531532290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039571 | ACTGAATGGTCAGGA[A/C]ACGCCACCTGAGCAC | 23510 |
rs531574107 | snp | C/T | 3.29549e-05 | 0.00405911 | intron-variant, synonymous-codon | ATP5H, KCTD2 | GRCh38.p7 | 17:75040155 | CACGGGAACCTTCAG[C/T]GCATTAAACTACAAA | 23510 |
rs531713701 | snp | A/G | 0.336017 | 0.234736 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044363 | GGCGCCCGCCACCGC[A/G]CCCGGCTAATTTTTT | 23510 |
rs531885681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062761 | CTTCTAAATCGTGGA[A/T]ACCAGGTAAGCTGGA | 23510 |
rs532057146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033827 | ACCCACTCCATGGAT[C/G]GCGCCTCTGTCAGGC | 23510 |
rs532125174 | snp | A/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031130 | TAAAATAAAATTGGA[A/G]TGATACAGAGAAGAT | 23510 |
rs532159768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060214 | ATAGGAAGGCCAGAG[C/G]GAATAGAGTAAATAC | 23510 |
rs532193478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035220 | ACTATAATCTTCCCT[C/T]CCTTGTTTTAGACCC | 23510 |
rs532250122 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75054831 | AAAAAAAAGAAGCTT[A/G]AAGTATAGCCAGGAA | 23510 |
rs532341857 | snp | A/C | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046336 | ATTCGCCCGCCTTGG[A/C]CTCCTAAAATTCTGG | 23510 |
rs532356037 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064520 | GAAATGACTGCAGAC[G/T]GTGCCAAATGTCTTT | 23510 |
rs532394237 | snp | A/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75051037 | GGAGTGCAGTGGCGC[A/T]ATCTCGGCTCACTGC | 23510 |
rs532416443 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065179 | GCACGTGCTCTGGGA[A/G]ATAGACAGGAGTGGT | 23510 |
rs532484300 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031276 | TCAGCAAATGCTAAG[G/T]GAATGCCAGGCACTC | 23510 |
rs532554745 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047686 | GCTCCTCACAGGCAG[C/G]CCCCTCAGGCCGGGA | 23510 |
rs532615747 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75046953 | GGCTGCCCACGGTCC[G/T]CCGCAGCAAGTAACG | 23510 |
rs532747468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055638 | CAGGAGTTCAAGACG[A/G]GCCTGACTAACATGG | 23510 |
rs532829560 | snp | C/T | 0.000131798 | 0.00811675 | intron-variant, synonymous-codon | ATP5H, KCTD2 | GRCh38.p7 | 17:75040140 | ATATTTATCCTCTGG[C/T]ACGGGAACCTTCAGC | 23510 |
rs532831975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061199 | AGACAGGCGGAGGCG[C/T]CCCCAGCCCCATCCT | 23510 |
rs532945302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044759 | TTTAAGTAAGATCAG[C/G]GTCAGATATTAAAAG | 23510 |
rs532957124 | snp | C/T | | | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060050 | CTAGGAAGGATCAGG[C/T]GCCATGGGAAGTGTG | 23510 |
rs533073652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050525 | GCCTCAGCCTCCCAG[A/G]GTGCTGGGATTACAG | 23510 |
rs533075854 | in-del | -/A | 0.211516 | 0.24702 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043612 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 23510 |
rs533213068 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75061057 | CTCTTAAGCAAAGGA[-/T]TTTTTTAATGTATTC | 23510 |
rs533289900 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036611 | AATGCTGGGGTTGCC[C/G]CCTTCACATCCCAAC | 23510 |
rs533348880 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75032629 | TGCCCAGGAGAGGGA[A/G]TGGAAACCTGGAGCT | 23510 |
rs533390904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055062 | AAATTATTCTTTTTT[C/T]TTCTTTTTTTGAGGC | 23510 |
rs533391601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049097 | GCCATCACTAAAGTC[A/T]TTTTTAGCTGATGGA | 23510 |
rs533472106 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056192 | AGCTGACAGCTCAAA[-/G]GCTCCTTTTTGATGT | 23510 |
rs533479423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043593 | ACTCCAGCCTGGACA[C/T]AGAGTGAGACTCTGT | 23510 |
rs533657377 | snp | A/G/T | 1.64746e-05 | 0.00287002 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039190 | CATATTATAGGCAAC[A/G/T]GCTACCCATCATCCT | 23510 |
rs533766385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034325 | CAAGAGAAGGCGAGG[A/G]GCGCAAACAGGGCAG | 23510 |
rs533829660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039653 | GTGCTTTCAAGCAAA[C/T]AATTAGGTATTTGAA | 23510 |
rs533881867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045621 | GAAGGAAGAGAAATA[C/T]GGCTCTGTTCTGCCC | 23510 |
rs533910634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055912 | AGCGGGCGCCTATAA[G/T]CCCAGCTACTTGGGA | 23510 |
rs533926758 | in-del | -/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75057557 | ATAGCTATACCTCTT[-/T]TTTTTTTTTTTTTTT | 23510 |
rs533949288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75061720 | GGTGCTTTCCAGAGC[C/T]TCCTGTCCCCAGTCT | 23510 |
rs534164555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062262 | TAAGGAGCCCCTTCC[A/C]TGGGCAGTTGCCTCT | 23510 |
rs534183720 | snp | A/C | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039614 | CTCTCTGGTGGAGCC[A/C]CTGAGTTCCATAGTT | 23510 |
rs534292110 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059705 | ATAACCACGGGAGAC[A/G]GCTACGGCCAGGTGG | 23510 |
rs534320484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033464 | TTGTACATTCCCTCA[A/T]GATAAGCAAGATTTT | 23510 |
rs534325006 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065214 | CCGCCCTCTCGGAGG[G/T]CTGGTGTTCACCAAG | 23510 |
rs534358519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044986 | CACCCTTACAGACTT[G/T]CCCAAACATCAGTGT | 23510 |
rs534407062 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064768 | GGCATCCATCCAGTC[A/G]TATCTTTCAGAGAAA | 23510 |
rs534437517 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051262 | GGATTACAGACATGA[A/G]CCACCGCGCCCGACC | 23510 |
rs534482427 | snp | G/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75033983 | CACCTGGGGTAGAGG[G/T]GAAAGTTCCTTTTAC | 23510 |
rs534527047 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037694 | ATCTCTATTGCCTGA[C/T]GTTGCTCAGGTCTGC | 23510 |
rs534545743 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048457 | AGTTGCGTAAACATT[C/T]GTTGTTTTCGTTTAT | 23510 |
rs534582727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053364 | GGCGCCCAGGGCACT[C/T]TAGGTCTAAAACCTG | 23510 |
rs534589901 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053310 | CCTATGTCCCAATAG[A/T]ATGAGAAGATTGTCG | 23510 |
rs534596607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054134 | GTGATTTTCCTACCT[A/C]AGCCTACCGAGTAGC | 23510 |
rs534668825 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047103 | GCACAGCGCCTCCCC[C/G]GCGCGGGTCCCCGGG | 23510 |
rs534880502 | in-del | -/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031207 | ACTCAGAGCCTAGGA[-/G]GGGGCTGAGGCTCAT | 23510 |
rs534888807 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75035243 | TTAGACCCAGAAACG[C/G]CTCCCAATCCCTCCA | 23510 |
rs535049493 | snp | G/T | 0.336017 | 0.234736 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044423 | TGTTAGCCAGGATGG[G/T]CTCGATCTCCTGACC | 23510 |
rs535108367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044067 | TTTCACTCTGTCCCC[C/G]GGGCTGGAGTGCAGT | 23510 |
rs535179577 | in-del | -/T | 0.243633 | 0.249919 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044024 | GCACACGTTGTGCAC[-/T]TTTTTTTTTTTTTTT | 23510 |
rs535184744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050120 | AAACAATATTTCAAA[C/T]GCATACAGAAGTAAT | 23510 |
rs535366381 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75038287 | TTACAGGCGCCCCCC[C/G]CCCCACCACCACGCC | 23510 |
rs535459158 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032116 | TTATTGTGGGATTTC[A/G]GTGAATAAATACGTG | 23510 |
rs535480259 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050558 | CTGAGCCTCCGCGCC[C/T]GACCTGAGATGTTTG | 23510 |
rs535545489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055917 | GCGCCTATAATCCCA[A/G]CTACTTGGGAGGCTG | 23510 |
rs535577272 | snp | C/T | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75035124 | CGGAGACCGCGTGGC[C/T]TAATGGATAAGGCGT | 23510 |
rs535618536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033875 | GACACTCGCTTATGA[A/G]GGGAAGGGATGGCAC | 23510 |
rs535645948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055399 | GCCTTGGTCTTTCTA[C/T]GTTAGATTTCATATA | 23510 |
rs535821881 | snp | A/G | | | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048062 | GCTTCCACAGCTGCA[A/G]GAAGCGCTCCTTGTG | 23510 |
rs535883028 | snp | A/G | | | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045791 | ACAGGGTCCTGGAAC[A/G]ATATACATCCTCAAC | 23510 |
rs535894789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036987 | GCTCTCCTCTGCTTA[C/T]GTTAAGACTACGCTG | 23510 |
rs535958219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042960 | GCGCAGTGGGCTCAC[A/G]CCTGTAATCCCAGCA | 23510 |
rs536067887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060946 | CGGAATCCACTCTGC[A/C]TGTGTCTGTCATCCT | 23510 |
rs536155278 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064245 | GGGCTGCATCCACAG[A/T]GTTTGTGTCCACACT | 23510 |
rs536155804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060630 | AGGTTCATGGCTGGG[C/T]GCGTGGCGAGTGGGC | 23510 |
rs536163163 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75032742 | AAGGCTGAGCCCCGG[C/G/T]CGGGCGGGTTGGGGG | 23510 |
rs536191023 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066160 | AGCTGGAAAGAGACA[A/C]GGGGAGGAGTGTGAG | 23510 |
rs536258843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062949 | TCATCGGGTCCAGTG[A/G]AAAGCATCCCCCGAC | 23510 |
rs536354228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034411 | ACCAAAAGAAACCTT[A/G]CGAGCACAGCCCCTC | 23510 |
rs536426768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052849 | CCGTGAGCCAAGATC[A/G]CACCACTGAACTCCA | 23510 |
rs536685966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054200 | TTTTTTGTATTTTGG[A/G]TAGAAACGAGCCTTG | 23510 |
rs536710793 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062685 | TCCCTCCACTGTGCA[-/C]CCCCCTCACCCCCAA | 23510 |
rs536725869 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75059947 | TGGGATTCGACAACA[A/C]TCCTTCCATTTCTTT | 23510 |
rs536818846 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040316 | GTCCCAAGCGGAAAC[A/G]AATACGCATCTCAAT | 23510 |
rs536875321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043030 | AGTTCGAGACCAGCA[C/T]GGCCAACATGGCAAA | 23510 |
rs536876707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045647 | TGCCCGGCTCACCGG[C/T]GGTCAGAGTTTAAGG | 23510 |
rs536935005 | snp | A/G | 1.71138e-05 | 0.00292516 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049194 | CCTCAAAGGTCCACA[A/G]TGATACCCTTGTGTT | 23510 |
rs537013938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050371 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 23510 |
rs537073123 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041007 | TCTGGATATTGAGAC[C/T]TGTGTAAATATCAGA | 23510 |
rs537076850 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047827 | CGTTCTCTGAGACTC[C/T]TTCCCACACTGCGCC | 23510 |
rs537212376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043805 | GCCTTAAATAGAGCA[C/T]TCTCTAGGCTAAAAT | 23510 |
rs537286183 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031054 | TGCAGTGAGCCGAGA[A/T]CGCACCACCACACTC | 23510 |
rs537348285 | snp | A/C | 0.00119737 | 0.0244387 | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75035316 | CCAATCAGGCTTTGC[A/C]TCCCGGGACGCTTCC | 23510 |
rs537357532 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031594 | ACAGCAAAGGCTAGG[A/G]AAATGGCAACTCCGA | 23510 |
rs537541327 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047206 | GCCGAGAAATGGGCC[C/G]GCCCGGCTGCGCGCG | 23510 |
rs537555331 | snp | A/G | 0.350764 | 0.228794 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044485 | GCTGGGATTATAGGC[A/G]TGAGCCACCGCGCCC | 23510 |
rs537650504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75062353 | CCTGGCCTTCTAGAG[C/G]CAGCGTTGCATTTTC | 23510 |
rs537653436 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064930 | AGCAGCTTGGTTTGC[A/G]GCCTTGTGCCCAGTC | 23510 |
rs537683216 | snp | A/G | | | downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75066231 | TCTGTCACCCAGGCT[A/G]GAGTGTAGTGGTGCA | 23510 |
rs537689005 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034296 | ACCACCGCGACTGCA[A/G]ACAGAGGGTCCTGCA | 23510 |
rs537771830 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033891 | GGGAAGGGATGGCAC[A/G]GCCACGTGCCCCAAG | 23510 |
rs537814270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060993 | GGGTTGTAAAACGTC[A/G]CCAAGAGTTTAATGC | 23510 |
rs537830042 | snp | A/G | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75037309 | AAATCGTGCCACTGC[A/G]CTCCAGCCTGGGCGA | 23510 |
rs537831751 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064822 | AAAGTAGTGATCACG[A/G]GAAGGACTGCTCTGA | 23510 |
rs537833800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039117 | AGACGGAAAGCAGAA[A/T]ATCCAAGGCAGGTTC | 23510 |
rs537891100 | snp | A/G | | | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75035266 | TCCCTCCACACCGCG[A/G]CTCCCGGGATCCGAA | 23510 |
rs537896836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044921 | TCCTGTTGTGGAGGG[A/G]AGGTGTTAAGGCAAT | 23510 |
rs537953537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051221 | CTGACCTTGTGATCT[A/G]CCTGCCTCAGCCTCC | 23510 |