SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs71516775 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275931 | TGTCTTTAGCCCGAC[C/T]TAAATTCCAGCCTTA | 286053 |
rs71516776 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321095 | CCATGATCCAGTCAC[A/C]TCCCACCAGGCCCCA | 286053 |
rs71516777 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333500 | ATGTAGTTTTCCTGG[G/T]GGTTCTTTTTTTTTT | 286053 |
rs71516778 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343901 | GTCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 286053 |
rs71516779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359965 | AAAGTCAGTTAGGAT[C/G]CTTTTACAGTGGTTT | 286053 |
rs71516780 | snp | G/T | 0.0452528 | 0.143452 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367239 | ATGTCTTTCAGCCAG[G/T]TGCAGTGGCTCATGC | 286053 |
rs71576767 | in-del | A/CCCC | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094091 | TTATAGGCATGAGCC[A/CCCC]CCACACCCAGCCTGA | 286053 |
rs71576770 | in-del | -/CA | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143098 | CAGTGTGGGTGCACG[-/CA]CACACACACACACAC | 286053 |
rs71576771 | in-del | -/GGCAG | 0.495228 | 0.0529803 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161725 | CGCTTGAACCCAGGA[-/GGCAG]GGGTTGCAGTGAGCC | 286053 |
rs71576772 | in-del | -/AATT | 0.494568 | 0.0518327 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192526 | TATGTATATGGTAGC[-/AATT]AAATAGGGAAAAAAC | 286053 |
rs71576775 | in-del | -/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260671 | CTCTGTTACCCAGGC[-/T]TGGAGTGCAGTGATG | 286053 |
rs71576776 | in-del | -/TTT | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299804 | ATAATTTTGGCTTTC[-/TTT]TTTTTTTTTTTTTTT | 286053 |
rs71576778 | in-del | -/A | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348493 | GGAGCATTGGAACTT[-/A]ATATGGTTTGGCTGT | 286053 |
rs71576779 | multinucleotide-polymorphism | CC/TT | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125362019 | AAGACCCGGTTCCCT[CC/TT]GCTCAGCAGTCACCT | 286053 |
rs71735628 | in-del | -/CTT | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184347 | AAATCATGGCTATTA[-/CTT]CTTAAATCTCTCTAA | 286053 |
rs71982432 | in-del | -/AATT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192527 | ATGTATATGGTAGCA[-/AATT]AATAGGGAAAAAACT | 286053 |
rs72031823 | in-del | -/T | 0.34101 | 0.232846 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103992 | TTGGATTTTGTTGTC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs72085790 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341898 | AGGATCTAGAAATGG[-/A]AAAAAAAAAAAAAAA | 286053 |
rs72131110 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181707 | GGAGGGCCAAAAAAA[-/A]AAAAAATGTTGAGCA | 286053 |
rs72223702 | in-del | -/CA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143099 | CAGTGTGGGTGCACG[-/CA]CACACACACACACAC | 286053 |
rs72261443 | in-del | -/ATAATA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275000 | GACAATCTGAAGATG[-/ATAATA]ATAATAATAATAATA | 286053 |
rs72476060 | in-del | -/TT | 0.132551 | 0.220694 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217359 | ATTTATTTATTTTTT[-/TT]ATTTATTTATTTTGA | 286053 |
rs72537278 | in-del | -/GAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304964 | AGGAAGRAAGAAAGA[-/GAA]AAGAAAAAGGAAAGG | 286053 |
rs72720529 | snp | C/T | 0.150333 | 0.229274 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090695 | TACAGAATAATATTT[C/T]TTAAGGAAATCGAAT | 286053 |
rs72720531 | snp | C/G | 0.0865458 | 0.189163 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098327 | CTAACAAGTTCATAG[C/G]TGATGCTGGTGACAC | 286053 |
rs72720532 | snp | A/G | 0.175897 | 0.238765 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099640 | GTCAAAGGAGATAGG[A/G]CTGAGCATTGATAAC | 286053 |
rs72720533 | snp | G/T | 0.144969 | 0.226867 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104014 | TTTTTTTTTCAGCCG[G/T]AATTTTGCTCTTGTT | 286053 |
rs72720536 | snp | C/T | 0.140242 | 0.224618 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124023 | TCAAAAAAAGAAACC[C/T]TGTACCCTTTAGCTA | 286053 |
rs72720538 | snp | A/G | 0.139225 | 0.224118 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134751 | TTTTTTTTAAGAGTC[A/G]GGGTCTTGCTCTGTT | 286053 |
rs72720547 | snp | A/C/G | 0.141995 | 0.225653 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145014 | TTTAGGAAAATCATA[A/C/G]GCAGGCCAACTTCAC | 286053 |
rs72720550 | snp | A/G | 0.136166 | 0.22258 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157989 | AATGTGCTTTTATGC[A/G]ATGTGATTCTCCAAA | 286053 |
rs72720552 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166202 | TTGAAAAAATGTTAC[A/G]ATCTCAAAATAGATG | 286053 |
rs72720553 | snp | A/G | 0.136847 | 0.222927 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168339 | AAACACTGGGAGGAG[A/G]ATGGAAGAAAAGGAA | 286053 |
rs72720554 | snp | A/G | 0.141258 | 0.225111 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168640 | CTCTTTTATGATGGC[A/G]CAAGTCCCATTAATG | 286053 |
rs72720555 | snp | A/G | 0.188 | 0.24219 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171663 | AATTGCTTCTGACTT[A/G]TTCATCTCTTCTACC | 286053 |
rs72720560 | snp | C/T | 0.143959 | 0.226396 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219920 | CTCTTTTTCTTTCTT[C/T]TTCTTTCCTAATACA | 286053 |
rs72720563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225935 | ATTTCCAAAAGATGA[A/C]TTTTAATGGACTTTT | 286053 |
rs72720566 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233834 | ATCTTCACTTTTTCC[A/G]CTGTCACTTTCTACA | 286053 |
rs72720569 | snp | G/T | 0.150333 | 0.229274 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246165 | TTCAATCTGCAAAAT[G/T]AATCTTTTCTTTTTT | 286053 |
rs72720571 | snp | C/T | 0.271972 | 0.249033 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253390 | GGCTTTCTTTTCGCC[C/T]TGAGCAAAAAAGATG | 286053 |
rs72720574 | snp | C/T | 0.275464 | 0.2487 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260443 | ATATCTCTATACTTT[C/T]GTGTGTGGTAGTTGC | 286053 |
rs72720581 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283111 | AGTAATAATATCTAC[A/G]TCATAGAGTTATGAC | 286053 |
rs72720586 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298632 | AATTAAATGGAATAC[C/T]ATTGAACGTGACCAG | 286053 |
rs72720592 | snp | A/G | 0.206642 | 0.246211 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319821 | CAGTCTCAAGGAGTC[A/G]CATATATGTTTTAGT | 286053 |
rs72720595 | snp | C/T | 0.26271 | 0.249677 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330239 | TGGAGTGCGATGGGA[C/T]GATCTAGGTTCACTG | 286053 |
rs72720596 | snp | C/T | 0.206947 | 0.246265 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333238 | ACAGTGGCACGATCA[C/T]GGCTCACTGCAGCTT | 286053 |
rs72720597 | snp | A/G | 0.195214 | 0.243923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334583 | CCCCCTGCTGGAGGG[A/G]AATTGTTTTTCTCAC | 286053 |
rs72720601 | snp | A/C | 0.206029 | 0.246103 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342608 | AAAGATTTTCCTCAT[A/C]TTTTAGCTCCTTCCT | 286053 |
rs72722603 | snp | A/G | 0.195526 | 0.243993 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350767 | CAGTTGCCTCTCATT[A/G]GGTCCTTCCCACAAT | 286053 |
rs72722605 | snp | C/G | 0.195214 | 0.243923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355964 | TTCTCAAAGTGCAGG[C/G]CAGGGATCTCTAGGG | 286053 |
rs73336833 | snp | G/T | 0.0644693 | 0.167566 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293973 | ATTTACTTCCTATTT[G/T]CTCCCAAGTTCCCCA | 286053 |
rs73336837 | snp | A/G | 0.166832 | 0.235761 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297631 | AAGCCAGCAGTTCGA[A/G]ACCAGCCTAGGCAAC | 286053 |
rs73336855 | snp | A/G | 0.084364 | 0.187256 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328099 | TGGCCATTTTTCCAG[A/G]TTGTATAGTCACTTT | 286053 |
rs73336862 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332152 | ATTTATTATCCTCTT[C/T]CCATTTGAATAAATT | 286053 |
rs73336865 | snp | A/T | 0.163892 | 0.234703 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336525 | AGAAGCTATGAGAGG[A/T]TGATGAGGATCAGAG | 286053 |
rs73336867 | snp | A/G | 0.196771 | 0.244268 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340320 | TGTCATTGTGAAACT[A/G]GGTTAAAATTTCAAA | 286053 |
rs73336869 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340942 | CCTCCTTGATGTTCA[C/T]CTTTCATTTATTTTT | 286053 |
rs73336877 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344107 | TTACCCAAATTGAAA[C/T]GTTGCAGTTTTAAAG | 286053 |
rs73336879 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345652 | TCTGCTTTAGCACCT[C/G]ACAGAGGAAATGCCT | 286053 |
rs73336884 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346552 | TGGCTAATCAGACTT[C/T]CCCTATTATTTGGTT | 286053 |
rs73336887 | snp | A/C/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346750 | TATGACCAAATCTTA[A/C/G]CTGACGATTTTTGTC | 286053 |
rs73338849 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347142 | TAATCCTCAGACAGC[A/G]CTATGAAGTAAGTAC | 286053 |
rs73338850 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348050 | TCCACAGTATCTTGT[A/C]TATGCATGACCTTCA | 286053 |
rs73338855 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351340 | CCTTCCTTTTGGTGT[A/T]CATTTTGTGACATAA | 286053 |
rs73338856 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352822 | TGACCTTTTGTTAGC[A/G]CACTGGAGAATCCCA | 286053 |
rs73338858 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352998 | TTTTGTTACCTTTTT[A/C]TTTCGTGATCACTGA | 286053 |
rs73338860 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356793 | ACTGTTTATTGATTA[C/T]TGCTTTGTACCATGA | 286053 |
rs73338863 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357058 | GAATGAGGTACCCCG[C/T]AGTGTTCTCTGAAAA | 286053 |
rs73338869 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363063 | AAAGCAGATATTCAG[C/G]GTTATGTTTTAAGGG | 286053 |
rs73348119 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097627 | ATAATCCTTTCCTTT[C/G]TTGAACATTGTAGCA | 286053 |
rs73348122 | snp | C/T | 0.247905 | 0.249991 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101216 | TATGAGTGAAATGAA[C/T]GAATGAACCTAATTA | 286053 |
rs73348129 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109503 | TTAGTTTTATGAGAT[C/T]GTTGACTTTTTGGGT | 286053 |
rs73348132 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111452 | ATAACCCTATCACCC[A/G]TCACCTTATTTTATG | 286053 |
rs73348137 | snp | C/T | 0.111576 | 0.20818 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116059 | CCAGCCCCATGACCT[C/T]GATTTATCTGTAGTC | 286053 |
rs73348148 | snp | A/G | 0.243061 | 0.249904 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128105 | TTGAGCAGAAGCTGG[A/G]GAGACTTGGAGAGGG | 286053 |
rs73348163 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136739 | AGTTTTTTTGAGGCT[C/T]CTGGTAGGTTTAGGT | 286053 |
rs73348178 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151732 | AAAAATAAAGAAGAT[C/T]GGTATTTTGGTTTTT | 286053 |
rs73348180 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152174 | TTGACTAACTTTAAG[A/G]ATATCACCTATATCC | 286053 |
rs73348181 | snp | A/G | 0.261884 | 0.249717 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152326 | ATTTGAAACTGGATG[A/G]CACTTAGACTAGAGG | 286053 |
rs73348183 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154054 | TTATTTTTTTAAAAG[A/G]CAATTAATGGGAAGC | 286053 |
rs73348186 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156108 | AACATAGTAAGACTC[C/T]ATCTCTTTAAAAAAA | 286053 |
rs73348187 | snp | C/T | 0.301429 | 0.244653 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159725 | ATTAGTCTCAAATTG[C/T]TCAGTTGGTGGATCA | 286053 |
rs73348190 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163757 | AAGGGAGTCCCTGTT[A/G]GCTCTTAGAGGAGGA | 286053 |
rs73348195 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168119 | TTTCTATGAAAGATT[G/T]TATTTTTTTTTGTGG | 286053 |
rs73348196 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168443 | GCCTACTGTAATGGA[A/G]TACCATAAACCAGTA | 286053 |
rs73348200 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171209 | CACTTATACCATTTA[A/G]CTAGTTACGTATTTT | 286053 |
rs73349807 | snp | A/G | 0.00061472 | 0.0175209 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182064 | GTTAACACTATTATT[A/G]TTAACATTTAACTCA | 286053 |
rs73349809 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182490 | CAGAAAATTTCCCAG[C/G]AGCTAGTTATGTGTA | 286053 |
rs73349872 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188285 | TGTAGTTGCACAAGG[G/T]TAGTGGTTTTTATGT | 286053 |
rs73349877 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194203 | GTCCTGCACAGTTCT[A/G]TCAATCAACCCCCAA | 286053 |
rs73349892 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202187 | TCGTGAGGCAATGCC[C/T]CGCCCTACTTCACCT | 286053 |
rs73349893 | snp | C/T | 0.254105 | 0.249966 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203030 | CTTCCTATGCTCTGA[C/T]GAAAACATGAATATT | 286053 |
rs73349896 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204650 | CTGTAGAGCACAGGG[C/G]TTTTACTTTACATTT | 286053 |
rs73351205 | snp | A/G | 0.243347 | 0.249911 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209732 | TGACTAATACTGTCT[A/G]ACTTAATTGCTACCA | 286053 |
rs73351208 | snp | A/G | 0.24449 | 0.249939 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212042 | TTAGCCTAAGTGGGC[A/G]AAGTCCATCTGTCTC | 286053 |
rs73351210 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214247 | GTCAATAGCAGGCCA[A/G]TCGTTGGAAGGCAGA | 286053 |
rs73351233 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248156 | ATTAAAAATTGAAAC[C/T]AAAGTGTGAAAAGAA | 286053 |
rs73351234 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250569 | ATTCAGATTTGTCTT[A/C]AATTTTTATAGCTAT | 286053 |
rs73351251 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258918 | CTTTGTTTTCTGTTT[C/T]TGAGACAGAGTTTTG | 286053 |
rs73351278 | snp | C/T | 0.17138 | 0.237316 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286693 | AGCCACTTTCATGTC[C/T]ATGAACTTGCTTAAG | 286053 |
rs73704533 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106093 | ACTAATACCAGGAGT[C/T]AAAATAACAAAGTAG | 286053 |
rs73704534 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112162 | CCAACTATACCAGCA[A/G]AATAGCATTATAACT | 286053 |
rs73704537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128597 | AACAACACAAATCTC[A/G]AGCCTGAAGTGAATC | 286053 |
rs73704539 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136780 | TATTACTATTTTTCA[A/G]TAGGAAGCTTTTAAA | 286053 |
rs73704540 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138746 | ATCCTGGGAAGCAAA[A/G]ATTCGCAGGGTAGGA | 286053 |
rs73704541 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143644 | TGTTCCTGTTCAGAC[A/C]TGCCTGTACATGGCT | 286053 |
rs73704542 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149355 | AAAAGCCAAATGTGA[A/G]TGGACTTTACATTAT | 286053 |
rs73704543 | snp | G/T | 0.237303 | 0.249677 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151733 | AAAATAAAGAAGATC[G/T]GTATTTTGGTTTTTC | 286053 |
rs73704544 | snp | A/T | 0.0799831 | 0.183287 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162919 | TTATTCCTGTCTACC[A/T]TCCTGCCCCCTCAGA | 286053 |
rs73704546 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165655 | CTAATCACTGAGAAT[C/T]AAAATTATATACATT | 286053 |
rs73704549 | snp | A/G | 0.240478 | 0.249819 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173826 | ACATTTAAGGTGAAC[A/G]GGGGTTTGAGTAAGT | 286053 |
rs73704550 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191959 | AATACGTTCACAAGG[A/G]AAGGGGAAGTTTTAA | 286053 |
rs73704554 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207626 | TTGTGGAACAAACCA[C/T]CCCAAAACGTAGTAG | 286053 |
rs73704556 | snp | C/T | 0.238749 | 0.249747 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211918 | TATATTCCTTAACTT[C/T]CAGGAGAGTTCTAGT | 286053 |
rs73704560 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248227 | CTTTTCAGTCATGTC[A/G]GAAGGAAGCATGCTT | 286053 |
rs73704562 | snp | A/T | 0.0995161 | 0.199636 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254163 | GACTCCAATATTACA[A/T]TTAATAATTCAAACT | 286053 |
rs73704563 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257852 | CAAAACCAAATGTCA[A/G]TGGATAAGTGCATGG | 286053 |
rs73704564 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258441 | GGGAATGCCCCACCC[A/C]TATCCCATTCACCCC | 286053 |
rs73704566 | snp | A/T | 0.0759472 | 0.179459 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263041 | GGCGACAGGGACCTC[A/T]TAATGAGGTAGCTGG | 286053 |
rs73704568 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286255 | CCAAAAAATTATCCA[A/G]TGGTCCATCTCTTCC | 286053 |
rs73704912 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295250 | CTTCTGGGGCCCCTA[A/G]TCTGGTGACCTTTGT | 286053 |
rs73704916 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297447 | TTCTAAATGGGGGAA[A/G]TGGTTTCCTTTGTTC | 286053 |
rs73704921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305297 | CATTTTACTACTGTG[A/G]AAACCTAAACTCAGA | 286053 |
rs73704922 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306536 | TTTGAGTCAAATGTA[C/T]ACACTGAAATTTCTT | 286053 |
rs73704923 | snp | C/T | 0.046775 | 0.145601 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308776 | GCAGGCCTCCCATTC[C/T]GGTGAGTGTAGCTCA | 286053 |
rs73704925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311230 | TACCAAAGAATAGAA[A/G]CCATGAAGAAAACCA | 286053 |
rs73704928 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327871 | TACAGAGATTCTTGA[C/T]ATCTCTAAATGGGTC | 286053 |
rs73704930 | snp | A/G | 0.144632 | 0.226711 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330682 | AAGCCTCGAATGTAC[A/G]CTAGGTACTAAAGGA | 286053 |
rs73704932 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335143 | AGTGAAGTCCCAACA[A/G]GACTCTGAGAAGGAA | 286053 |
rs73704933 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335159 | GACTCTGAGAAGGAA[A/G]CCACCCACTCAGAAT | 286053 |
rs73704935 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338147 | CATGATGTGACCTCC[C/T]AGGTCACATAGCTGA | 286053 |
rs73704936 | snp | A/C | 0.0755793 | 0.179102 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338886 | ACATCTTAGCATCTC[A/C]GTTTAGGCCAAAGAT | 286053 |
rs73704939 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351051 | CAGAACCTACTAGTG[G/T]ATTGGATGTGAGGAA | 286053 |
rs73704940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358032 | AGGGAACTTCAACCA[C/T]ACCTTCAAAACAGAA | 286053 |
rs73704952 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364589 | AACCTAGCATAGGGC[C/T]GATCCCTAGAAGAGT | 286053 |
rs74275597 | in-del | -/AAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349597 | TTAAAAAAAAAAAAA[-/AAA]GAAAGAAAAGAAAAG | 286053 |
rs74315899 | snp | A/G | 0.188631 | 0.242351 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271578 | GATTCAGTCCCTGAC[A/G]TGACTCCTAGCTGTT | 286053 |
rs74320623 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238600 | TTTCCTGTTCCTCCC[A/C]CTTTCCCACCAGCTT | 286053 |
rs74343026 | snp | A/C | 0.101658 | 0.201233 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246641 | CTTTGAAGGAACACA[A/C]ATGTCCTATGTTATC | 286053 |
rs74344708 | in-del | -/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321267 | CACACAGGATTTTTT[-/TT]CTTAATATTCTAACC | 286053 |
rs74379244 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096647 | TCCTTTTTTTTTTTT[C/T]TTTTTTTTCATACGG | 286053 |
rs74411034 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349059 | CACACACACACACAC[A/G]CACAGAGCTCTTAAT | 286053 |
rs74422702 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326957 | GCAAAACTCCATTTC[A/C]AAAAAAAAAAGAGAG | 286053 |
rs74423150 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303918 | TCACCTACTTCTTGT[A/G]CTGGCTAAAGAAACA | 286053 |
rs74456568 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126962 | TTATTTGGTTCTTTC[G/T]CAGGTGAGAGAGGTG | 286053 |
rs74457361 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271667 | GAGTGCTGAATAGGT[A/G]TGAATCAGGTTTCAT | 286053 |
rs74476075 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174170 | ACTTTTTATAGTTTG[A/C]AATAATCTGCTTGAT | 286053 |
rs74477429 | snp | A/G | 0.0505692 | 0.150756 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129152 | AGCCATAGAATGAAT[A/G]TTTGTTTCTTAGGTG | 286053 |
rs74481992 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097327 | AAATTTCCATGATGA[C/T]CACTAGACCCAACTG | 286053 |
rs74484427 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337274 | ATTGTTGCTGACTTG[C/T]AACCCTACACCCCCT | 286053 |
rs74490237 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115188 | TAGAAGCCACGGTAG[A/G]AATATTGACTCCACC | 286053 |
rs74493457 | snp | A/C | 0.140919 | 0.224948 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156722 | CTATTGAAACCAAAG[A/C]AATCTTAGATATAAT | 286053 |
rs74510478 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107188 | TTTATCAAGGACATT[C/T]TTTTTTTTTTTTTTT | 286053 |
rs74529098 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236830 | TTCTTTTTTTTTTTT[C/T]TGATCTTGCTCCTTT | 286053 |
rs74530093 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122633 | AAGTATCATCTTTTT[C/T]CTGCAGACATTCCTC | 286053 |
rs74547307 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238068 | ACCTCATTTCTAGTC[C/T]TGGCTTCACAGCCTC | 286053 |
rs74558696 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352082 | ACAATATAGTTATTC[C/T]TCATGGGTATTTTGT | 286053 |
rs74559213 | snp | G/T | 0.0505692 | 0.150756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126953 | TGCTTATAATTATTT[G/T]GTTCTTTCGCAGGTG | 286053 |
rs74570397 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168527 | TGATGAAGGTGCTGG[C/G]ATGTTCAGCATCTGG | 286053 |
rs74596664 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119726 | GACATAAAATTTTAC[A/G]TCTTCTAGTAAGCAG | 286053 |
rs74609311 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160604 | GAACTTCCCTGATAG[C/T]CACCCTCCCTATGTC | 286053 |
rs74632517 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315111 | CTCATTGACTAGAAT[C/T]TTTTTTTTTTCTTTT | 286053 |
rs74636722 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272885 | CGTATACGTGTGTGT[A/G]TATATATATAAAAGG | 286053 |
rs74660548 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262913 | CAGTGGTTTTGACCA[C/T]TTCAGTGCCTCCGCG | 286053 |
rs74664999 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212265 | AATAAGATTTTATGA[C/T]CTGTTTTCTGGTAGC | 286053 |
rs74665435 | snp | C/T | 0.079617 | 0.182947 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267821 | GGTCATGTTGAATTA[C/T]AGAAGACTTCTGAGT | 286053 |
rs74678110 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196551 | CTTTTTTATGGCTGC[A/G]TAGTATTCCACGGTG | 286053 |
rs74681210 | snp | C/T | 0.13446 | 0.221699 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090076 | TCTCCTGCTAAGTTT[C/T]TGAAGATGGAAGAAG | 286053 |
rs74682494 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263751 | CGAGACTCCATCTCA[A/C]AAAAAAACAAAAAAA | 286053 |
rs74686660 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150651 | CCTCCCAAAGTACTA[A/G]GATTACAGACGTTAG | 286053 |
rs74735124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230202 | AAGAGATTCATCCAG[A/T]TATCAGATATCTTTA | 286053 |
rs74741509 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316091 | GGATTATAGGTATGA[A/G]CCACTACACCTGGTC | 286053 |
rs74770602 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207164 | ACCAGTTTTTTTTTT[C/T]CTCTGCTTCTACTTC | 286053 |
rs74785124 | snp | A/G | 0.167484 | 0.23599 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113015 | TATTTAATTTTTGTC[A/G]ATTAAAAATAAATTT | 286053 |
rs74790374 | snp | C/T | 0.26518 | 0.249539 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276566 | CTTCATAAAGGCAGA[C/T]GCATATGGTTATTAT | 286053 |
rs74819584 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297300 | TGAATCTGTAGAGCT[G/T]ATTTTACCCAGTTTT | 286053 |
rs74833493 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099153 | TTTAAGGAACTTACA[A/G]TGTAATTGGGGACTA | 286053 |
rs74841365 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341685 | AATTTGACACCTATC[C/T]CCCAATTTATGGTAG | 286053 |
rs74854706 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203088 | AGCTATCACTATGTA[C/T]TCTGTGGGCCTTTAA | 286053 |
rs74871622 | snp | C/G | 0.0622301 | 0.165053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111382 | AAGACATTCTTAAAT[C/G]TAGAAATTTGGTAAG | 286053 |
rs74895244 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105052 | ATTCCTCCTCCCTTG[C/T]GCAGGGAGGAGGCCA | 286053 |
rs74928156 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344188 | GACTTTATTTCATCA[G/T]TTGTTTCAATTTGAC | 286053 |
rs74935002 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126799 | GCAGTTAACATCTAA[C/T]AAGTATTTAACTTTG | 286053 |
rs74940380 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148966 | ATGATTTTTAACAAA[C/T]GGTTGCTGTATATAT | 286053 |
rs74941827 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236829 | TTTCTTTTTTTTTTT[C/T]CTGATCTTGCTCCTT | 286053 |
rs74976307 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173972 | TTTGAACCACTCAGA[C/T]GAAAGGTGCTGTGTA | 286053 |
rs74995245 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196427 | CTCACTCACAGGTGG[C/G]AATTGAACAATAAGA | 286053 |
rs74997964 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288052 | GCTCTTCACGAACTT[A/C]TGGCCTCAAGCGATC | 286053 |
rs75027683 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320988 | CAGGAGGAAGAGAGA[A/G]GGGCTACGCACTTTT | 286053 |
rs75028448 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179294 | AGTAAACTGTGATCA[C/T]GCCACTGTACTCCAG | 286053 |
rs75051008 | snp | A/C | 0.0741063 | 0.177655 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239945 | GTCGCCCACTCTGAT[A/C]CCTGCCCCTTCTTGC | 286053 |
rs75052412 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231232 | CAGTAGGGTGACCTA[A/G]TACACAGAAAGTGCT | 286053 |
rs75066603 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310447 | GAGTGCCCAATCAAT[G/T]GTAGCTATTGCAATT | 286053 |
rs75069409 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232364 | GTGAAACTCCGTCTC[A/C]AAAAAAAAAAGAAAG | 286053 |
rs75098398 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125185 | CTTTTTCTTGCCTAA[C/T]TGTCCTCGATAGAAC | 286053 |
rs75123658 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237611 | TGATAGAGTAATTCA[C/G/T]TTATGCCCTATTCTG | 286053 |
rs75130186 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187319 | GATAACTGAGTTAGG[A/G]AACAATTTCACAGAG | 286053 |
rs75132020 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324520 | CAAGGTGCCAGACCA[A/C]AAAAAAAAAAAAAAA | 286053 |
rs75158156 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288534 | TATTTCTCAAATCTG[G/T]CCTCTCTCTATGTCC | 286053 |
rs75161487 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239806 | CTTACATACATTTTA[C/T]CAAAGTGCATGAGAT | 286053 |
rs75169047 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231631 | GATTAGAAAACACCA[A/G]TGTGTATCATGCATA | 286053 |
rs75174580 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356345 | TTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTC | 286053 |
rs75228267 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281179 | TAGCTAGCTCTTTTC[C/T]CAACTGTGCAGAACA | 286053 |
rs75229409 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253519 | TTTTGACTTTCCATT[A/T]TCCACTTTAACTGTG | 286053 |
rs75236492 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204850 | TGCTGTCAGCCTCCT[A/G]TATGCTCCCAGCTCT | 286053 |
rs75314396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339032 | CTTACCCTGAGACAT[A/C]CTGTCAAAACTGTTC | 286053 |
rs75315087 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301977 | CCAATTTTTTTTTTT[G/T]GAGACCGAGTCTCAC | 286053 |
rs75328887 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108044 | GTCTCAAAAAAAAAA[A/T]AAAAAAAATTATGAT | 286053 |
rs75328923 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203000 | GTGTCAGGAATTGCT[C/G]TATTCACCATGAACC | 286053 |
rs75358093 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149786 | TATTTGTGGATCTGT[C/T]TCTGCTGATTGTTAT | 286053 |
rs75370313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289857 | AACTACTGGTCTTAA[A/G]TCAAAGCATTTATTA | 286053 |
rs75386687 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143959 | CCTTGTGGCTGAGAT[C/T]ATAGGAAACAGAGAG | 286053 |
rs75390137 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266110 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTTTTGCT | 286053 |
rs75393073 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096650 | TTTTTTTTTTTTTTT[C/T]TTTTTCATACGGAGT | 286053 |
rs75395316 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113972 | GGTTGTGAACCAAAA[A/G]AAGTAAATTCCCAGT | 286053 |
rs75433144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346809 | TATTTTAAACCTAAT[A/G]TTTGGACAGTATTTA | 286053 |
rs75434718 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302968 | ATTTTCCCCAGGGCA[C/T]GGAGCAGGGTAACGC | 286053 |
rs75441650 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312095 | AAAAAAAAAAAAAAG[A/G]AAGAAAAGAAAAGAA | 286053 |
rs75444425 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353016 | TCGTGATCACTGATG[C/T]TGGTAGCCACCTACA | 286053 |
rs75449920 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097806 | TATATGAAATGTATG[A/C]TTTAAGTCTTGGTGA | 286053 |
rs75463161 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254188 | CAAACTCTAATATCT[C/G]TATTGAAACACTCTG | 286053 |
rs75481712 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249519 | AAAAAATTTTGGGCA[A/G]AACATTTCTCTATTT | 286053 |
rs75492931 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180251 | AATTGAGCTTTATTC[A/G]TTCTTTAGCCATACA | 286053 |
rs75511192 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267522 | CAGGCATGGTGGCTT[A/T]CACCTATGATCCTAG | 286053 |
rs75518087 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189815 | ATATAACCCTTTACA[A/G]TGATATGTTGGCACA | 286053 |
rs75530622 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224751 | CAATAAGGTAGGTAG[A/G]TAGTGTTATCCCCAT | 286053 |
rs75538469 | in-del | -/T | 0.382473 | 0.212016 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132500 | AAAAAAAAATTTTGG[-/T]TTTTTTTTTTGAGAC | 286053 |
rs75553573 | snp | A/G | 0.0973687 | 0.197999 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089900 | TTATTACCTAGGTAA[A/G]TCACCTTTCTAAAAT | 286053 |
rs75559673 | snp | A/T | 0.122064 | 0.214785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317468 | TCCATAAGTTCTGGG[A/T]TTACAGGCGTGCACC | 286053 |
rs75563624 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192344 | GTTTTTTTTTTTTTT[A/T]AAAGAAAGTTTAAGT | 286053 |
rs75591567 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256285 | AGACTCCGTCTCAAA[A/C]AAAAAAAAAAAAACT | 286053 |
rs75600776 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336113 | GGTAGAAAGGAACCA[A/T]TGATATGGCTTTGAA | 286053 |
rs75611918 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253521 | TTGACTTTCCATTTT[C/G]CACTTTAACTGTGAT | 286053 |
rs75622842 | snp | A/G | 0.131723 | 0.220251 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090117 | ATTAGCTGAAAGAAG[A/G]AAATCACTTAGTTAC | 286053 |
rs75640995 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335524 | GAATATTAGAGATAG[G/T]TATGGATAGCCAGCC | 286053 |
rs75661639 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287486 | ATTGCTCTCCTGGCT[A/G]GAGATAACCAGAAGC | 286053 |
rs75664530 | snp | C/G | 0.375 | 0.216506 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196445 | ACCTATGAGTGAGAA[C/G]ATGCAGTGTTTGGTT | 286053 |
rs75680197 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265576 | GCTGCTATCTTTATT[C/G]AGTTTTTTGTTTTTT | 286053 |
rs75699748 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211262 | TGGTGAAAAGTGGGC[C/G]TCTGCCTCCCTGGAA | 286053 |
rs75701990 | snp | C/T | 0.194278 | 0.243711 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244431 | GGGGAAAGAAACCAT[C/T]CTGGAAGCATAAAAA | 286053 |
rs75724911 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292941 | TGTTGAAGACCCCCT[G/T]TAGTCTGGAGCAGTA | 286053 |
rs75734914 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186181 | TATATGAAAATTCTA[A/T]TTCAGTGTCCATAAA | 286053 |
rs75740508 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355954 | CACTCAGCAGTTCTC[A/G]AAGTGCAGGCCAGGG | 286053 |
rs75740827 | snp | A/G/T | 0.0318663 | 0.122387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227076 | CTGAGGCCACTCAGG[A/G/T]TCTGTATTAGAATTA | 286053 |
rs75770485 | snp | C/T | 0.0836354 | 0.186609 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195479 | CACATACATATAAGT[C/T]ACTTAGTAATTACCT | 286053 |
rs75775990 | snp | A/C | 0.0637235 | 0.166737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233727 | CGTGATAAGATTGTC[A/C]TAACTCCCAAATATA | 286053 |
rs75789746 | snp | C/G | 0.031825 | 0.122064 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205063 | AAACACTTAACATTC[C/G]TAGAAAGTACTGTGT | 286053 |
rs75798766 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296374 | TTTGGCTGTAGTCAA[A/G]TTGTTGTTGCCATGG | 286053 |
rs75799453 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176864 | CTTACCTGGGACTTG[G/T]ACCATTACTTCACAC | 286053 |
rs75804710 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097805 | TTATATGAAATGTAT[G/T]ATTTAAGTCTTGGTG | 286053 |
rs75815341 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291666 | GTGATGGTAAAGATA[A/G]AGGAGAAGACACCTA | 286053 |
rs75820550 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137719 | TTGAGGTAGTTAGGC[A/G]AATGGACTCTGTTAT | 286053 |
rs75831237 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232224 | AAAAATCAGCCGGAT[A/G]TGGTGGTGCATGCCT | 286053 |
rs75835883 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135446 | TTTGCTCTTGTATCT[A/G]AGAAATCTTTATCTA | 286053 |
rs75886683 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365122 | CACCGAGTCCCAGTG[A/G]CCCACTCAGTCTCTC | 286053 |
rs75896571 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196474 | TTCCTGTCCTTGCAA[C/T]AGTTTGCTGAGAATC | 286053 |
rs75897987 | snp | A/C/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196449 | TGAGTGAGAACATGC[A/C/G/T]GTGTTTGGTTTTCTG | 286053 |
rs75918233 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110984 | CTGTTTGGCTAAGCA[A/G]CAGCTCTCATGTTTG | 286053 |
rs75930082 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140969 | ATGAAAGACACCTGG[C/T]CGTGAAGATTTGGAG | 286053 |
rs75930542 | snp | A/G | 0.079617 | 0.182947 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296275 | TACATGACATATTGA[A/G]TGAATACTATGTTTG | 286053 |
rs75934468 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287548 | GACAACTTTCTCCTC[C/T]AGGACCTTGCCCTTT | 286053 |
rs75961301 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261720 | AAAATATCCACTTTG[G/T]TTAAAAGCTAATCAT | 286053 |
rs75984360 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123309 | TCCTTTCCAAAAGCC[C/G]TTTACATTTTCTGAA | 286053 |
rs75984474 | in-del | -/AA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181712 | GGCCAAAAAAAAAAA[-/AA]TGTTGAGCATGAAGG | 286053 |
rs75986522 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286262 | ATTATCCAATGGTCC[A/G]TCTCTTCCAGATTTG | 286053 |
rs75992477 | snp | G/T | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158278 | GGCCCTTTCTCCATT[G/T]CATTACTCCAACAGT | 286053 |
rs75994700 | snp | A/C | 0.0839998 | 0.186933 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101191 | ATTGACATGGTAGGT[A/C]CTCAATACTTATGAG | 286053 |
rs76011477 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316942 | TGCCACCACACCCAG[C/T]TGATTTTTGGTTTTT | 286053 |
rs76013183 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310624 | TCTGCATACCTGCAA[G/T]TACCTCATCCATTCT | 286053 |
rs76024466 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335050 | CGTGAGCCGCAGTAC[C/T]TGACCAGATTGCGAA | 286053 |
rs76028846 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322744 | TGCTAGAACTAATAC[A/G]TGAGTTTAGCAAATT | 286053 |
rs76038904 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115806 | ACCTGGGAGATGCTT[A/G]CTGATGCAACTGTTT | 286053 |
rs76046570 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290947 | TGTTTAATTCTCTAG[C/T]ACCTAGCAGTGCCCG | 286053 |
rs76047556 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305771 | TTTTTTCTGACCAAA[A/G]TATAGCCTTGTGCTT | 286053 |
rs76071519 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166288 | GTTGTTTTATTTTGA[A/G]ACAGAGTCTCGCTCT | 286053 |
rs76095707 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263749 | AGCGAGACTCCATCT[A/C]AAAAAAAAACAAAAA | 286053 |
rs76099198 | snp | A/T | 0.0543475 | 0.155628 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366076 | TTCTGGGTCCTGCCC[A/T]AGATAAGATGTGTTC | 286053 |
rs76101079 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218420 | AAATTGAGGGTTTTT[C/T]TTTTTTTTTGAGACA | 286053 |
rs76108213 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184298 | AAACACTTTCTAATT[A/G]AGAACATATAATTCA | 286053 |
rs76115358 | snp | C/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196369 | ACACACCAGGGCCTG[C/T]CGGGGCGGGGGTGCT | 286053 |
rs76138610 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265579 | GCTATCTTTATTCAG[G/T]TTTTTGTTTTTTGTA | 286053 |
rs76146700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194065 | TGACTGTATTTCATA[A/C]GGCATATTTTAGCTT | 286053 |
rs76148466 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228584 | TCACTGGGGAAGGCA[A/G]TACAGGGCATTTGAG | 286053 |
rs76151052 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176655 | TACTAACAGCTACTC[A/G]TTATTGAATATTTTC | 286053 |
rs76166283 | snp | A/T | 0.124444 | 0.216185 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116871 | TGATCCAGTTTTTTT[A/T]CTTAAGCATATAACT | 286053 |
rs76169540 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222710 | AATTTCTTTTTAAAG[A/G]CTAGCTAGTATTCCA | 286053 |
rs76198296 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196549 | TCCATTTTTATGGCT[G/T]CATAGTATTCCGTGG | 286053 |
rs76206666 | snp | A/C | 0.000636431 | 0.0178272 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102421 | TCCTTGAAAAACTTC[A/C]AAGCCTGTATCAACT | 286053 |
rs76207672 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207165 | CCAGTTTTTTTTTTT[C/T]TCTGCTTCTACTTCA | 286053 |
rs76209931 | snp | A/C | 0.0524604 | 0.153226 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337441 | CTTGGGCAATTATCT[A/C]TGTTGCTCAATTTAC | 286053 |
rs76213596 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158842 | GAAATAGACTGAACT[A/G]GGACTGGGGAATGGA | 286053 |
rs76232854 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268492 | GAGAATAAAGGAAAA[A/G]ATGGTATATTTCATT | 286053 |
rs76239118 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232363 | AGTGAAACTCCGTCT[A/C]AAAAAAAAAAAGAAA | 286053 |
rs76244848 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352565 | CCAGTCAGAGAAAAT[A/G]GAACAACACATTGAT | 286053 |
rs76252523 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164071 | ATTTGCACAGGGCTT[A/T]CTTAAGCCAGATTTG | 286053 |
rs76255826 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170738 | ACCTACAACATGTAT[C/T]TAGAGTCTAACCACC | 286053 |
rs76274724 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278865 | ATTTTATATCTAAGA[G/T]TATCTTCCTATTATC | 286053 |
rs76286469 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142477 | TGACTATAAAGGTGA[A/C]TACTTCTTGAGGATT | 286053 |
rs76304604 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208650 | TGATTGAGTGCCAGC[A/G]TAAGTGTTTCATACA | 286053 |
rs76320522 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140057 | ACTGTCCCAAGAACC[A/T]CACAGCAATGGTTGC | 286053 |
rs76320721 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231061 | TATCTAATATATATT[A/G]TTCTGGTTTCTTACT | 286053 |
rs76336358 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111803 | AGACCGTGTCTCAAA[A/G]AAAAAAAAATGGTTT | 286053 |
rs76344276 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150121 | CAGTTTTTCTGAAAA[C/T]AAGTTTGTTTTCTCT | 286053 |
rs76354357 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135662 | CACCATTTGTTGCTG[A/T]AGACTGTTTTTTCTC | 286053 |
rs76368133 | snp | G/T | 0.166832 | 0.235761 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110755 | TTAGATAATTTTGGT[G/T]GTTGTTGTTTTTTTT | 286053 |
rs76381272 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196500 | GGGACATGGATGAAG[C/T]TGGAAACCATCATTC | 286053 |
rs76408270 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329931 | CATGTAGTAAGACTG[A/G]TTGTTATTTTTTTTG | 286053 |
rs76420951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360706 | ACCAACTCCAGAAGT[C/T]TCTGATGAAGCATGA | 286053 |
rs76424712 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177828 | CAGAGTTCCTTTTGC[A/G]TCTCTCTTCTTTTTC | 286053 |
rs76436464 | snp | A/G | 0.17087 | 0.239388 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234812 | TATGGCCCTCTTCAG[A/G]TACCATTTTTATTTC | 286053 |
rs76449161 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154684 | TAGATCCTCAGAGAG[G/T]TCTATATGAACTTTT | 286053 |
rs76491300 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269909 | GCCTTCATTCAGTCA[C/G]TCATCCATTTATAAT | 286053 |
rs76499348 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263762 | CTCAAAAAAAAACAA[A/C]AAAAAAAAGAAGAGG | 286053 |
rs76499831 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282841 | TGTAACACAGTGTAC[A/G]GCCCTACTGGGCAGT | 286053 |
rs76530536 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111110 | TTCTGGCTAAGAATC[A/G]TCACCTTTTTAGATC | 286053 |
rs76537035 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301358 | AGAATGCAGTGGCTC[A/G]TGGTATCCAGCATCT | 286053 |
rs76540030 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141146 | ATTTTGAATTATACC[A/G]CTATCACAGTCATTT | 286053 |
rs76541191 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172185 | TCTGGTTCCAGGGTC[C/T]GTTGCCAGCCACCCT | 286053 |
rs76541842 | snp | C/G | 0.0225289 | 0.10389 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361768 | TTGTTATCACTCCCC[C/G]TGCTGCTTAGTGACA | 286053 |
rs76541851 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096451 | GGATTATTTTTTTCA[G/T]TGTAACCCATTATCT | 286053 |
rs76569864 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336111 | CTGGTAGAAAGGAAC[C/T]ATTGATATGGCTTTG | 286053 |
rs76575464 | snp | A/C | 0.133093 | 0.220981 | upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091888 | GGCAGGCGAAGGGGG[A/C]TGAGGAAAGGAGGTG | 286053 |
rs76577107 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191392 | TCTCTCAATTCAAGC[A/G]TACCATTCATTTCTT | 286053 |
rs76618080 | snp | C/T | 0.119978 | 0.213528 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349631 | AATGTTCCAGCCTAA[C/T]TGAAAAAGTACATAG | 286053 |
rs76621682 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196527 | TCTCTACAAAGGACA[C/T]GAACTCATCATTTTT | 286053 |
rs76637989 | snp | A/C | 0.0659589 | 0.169201 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226232 | TAACTAAATATTCTC[A/C]TGGCCCAGTCATTGT | 286053 |
rs76698778 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349759 | GTGGCCAGTACCAAA[C/T]GTATTTTATGACCAC | 286053 |
rs76709147 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203009 | ATTGCTGTATTCACC[A/G]TGAACCTTCCTATGC | 286053 |
rs76716508 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366299 | TAATCCCAGCACTTT[C/G]GGAGGCCGAGGCGGG | 286053 |
rs76728380 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134237 | CCAGACATTATGTTA[C/T]GAAGACTTCTGAGTC | 286053 |
rs76776916 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293714 | TAAACACTGAATGCT[C/G]TGAGAGATGATGGCT | 286053 |
rs76809644 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240143 | TTCTTTTTTTTTTTT[G/T]GAGACGGAGTCTTGC | 286053 |
rs76811742 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219884 | CATTACTGGACAAGA[A/T]GGTTCGTGCCATTCA | 286053 |
rs76819272 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244081 | TAGCAGTTGTTAACA[C/G]AGTGGTGTGCCATAA | 286053 |
rs76825647 | in-del | -/AA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126382 | TTTCAAAAAAAAAAA[-/AA]CGAGGGGGACAGTTA | 286053 |
rs76830391 | snp | A/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157729 | TATATTGAGACTGAT[A/T]TTCACCGTTACCTCA | 286053 |
rs76848984 | snp | C/T | 0.00589927 | 0.0539892 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125357283 | AGATATAATTGTGAC[C/T]CAAAGTCAGACCAAC | 286053 |
rs76855826 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139494 | TAGACTCATTATTCC[A/G]CATGGCTGGGGAGGC | 286053 |
rs76859259 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187871 | AGCTTAAAGGAGAAC[A/G]TATCATATTATCTTT | 286053 |
rs76876928 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092995 | TCTACAGATACTGCT[A/G]AATGTCCCCTTGCGA | 286053 |
rs76879212 | snp | C/T | 0.145978 | 0.227331 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188227 | TTTACTATTTTTAGT[C/T]GGTGGCTTTTCCGTC | 286053 |
rs76893915 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196564 | GCATAGTATTCCATG[A/G]TGTATATGTGCCACA | 286053 |
rs76894200 | snp | C/T | 0.0850919 | 0.187897 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093333 | TAGGATTTCAACATA[C/T]ACATTTTGGGTGACA | 286053 |
rs76901825 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152706 | AGAACGTTATGTTGA[A/T]TTTTTTTCCCTATTA | 286053 |
rs76906444 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135938 | TGTCAATTTCTACAG[A/C]GAAGTCGGCCAAGGT | 286053 |
rs76919413 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159095 | TCTGTCCTGTCTTCA[G/T]CACAAGAGGAAGGGT | 286053 |
rs76953477 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317190 | AAAGTCAGTGGTTTC[C/G]TAAAGATCTTTTTTT | 286053 |
rs76990021 | snp | A/C | 0.118933 | 0.212888 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362722 | TTCTGTCAGTAGGCC[A/C]TCCAGCTCCCCTTGG | 286053 |
rs77011513 | snp | G/T | 0.444444 | 0.157135 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110762 | ATTTTGGTTGTTGTT[G/T]TTTTTTTTTTTTTTT | 286053 |
rs77070647 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247724 | AGCAAAATTCTGTCT[A/C]AAAAAAAAAAAAAAA | 286053 |
rs77079254 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166987 | TGCACTCCAGCCTGG[A/G]TGACAGAGTAAGATG | 286053 |
rs77090051 | snp | A/G | 0.079617 | 0.182947 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269602 | GAATGTGAACATTCA[A/G]TGATCATAGCTTTCT | 286053 |
rs77099619 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134508 | TTTAATTTGATTTTT[C/G]TAATGATCATTAAAA | 286053 |
rs77113123 | snp | A/G | 0.0146788 | 0.0844035 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151154 | AAAATAATAATTGCA[A/G]TTTTTTTTTCTTTCA | 286053 |
rs77116195 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301978 | CAATTTTTTTTTTTT[G/T]AGACCGAGTCTCACT | 286053 |
rs77120204 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199028 | TCTGTGGGATTGGTG[A/G]TGATATCCCCTTTAT | 286053 |
rs77120988 | snp | A/G | 0.268452 | 0.249318 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257679 | GCTGGGACTACAGGC[A/G]CTCACCACCATGCCT | 286053 |
rs77121829 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164568 | CGTGTGTTAGAGAGG[A/G]ATTCTATTAGAATTA | 286053 |
rs77127112 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253522 | TGACTTTCCATTTTC[C/G]ACTTTAACTGTGATC | 286053 |
rs77140562 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119346 | TCACATTAGGATGTC[A/C]CTTTGTGAAACAGTA | 286053 |
rs77140875 | snp | G/T | 0.277778 | 0.248452 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348703 | ATGTCTTACATGGTG[G/T]CAGGCAAGAGAGAGA | 286053 |
rs77146565 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238601 | TTCCTGTTCCTCCCC[C/T]TTTCCCACCAGCTTC | 286053 |
rs77151592 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277525 | CTTTTTTTTTTTTTC[G/T]AGATGAAGTCTCGCT | 286053 |
rs77231072 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358333 | GCTAGACTCTGTCTC[A/C]AAAAAAAAAAAAGGT | 286053 |
rs77235354 | snp | C/T | 0.143284 | 0.226079 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342919 | CTAGATTTGCACCCT[C/T]GGGCTTTGATCTTTT | 286053 |
rs77253063 | snp | C/G | 0.162253 | 0.234095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177715 | ACTTAAGCTCACTTG[C/G]ATCATTTTCCCCAAA | 286053 |
rs77265311 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189013 | TTTTCCTAGAAACAT[A/G]TTGAGTGCATTTAAA | 286053 |
rs77268859 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335877 | TAGGTTGGTGTGTCA[G/T]CTAAAGAGACGATAT | 286053 |
rs77270247 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196397 | aacacttggacacag[G/T]gtggagaacatcaca | 286053 |
rs77286726 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, missense | NSMCE2 | GRCh38.p7 | 8:125362101 | GGTGGGGACCCAGCC[A/G]CTCCTGCGAGGCCTG | 286053 |
rs77298203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293903 | GCAGCCATCACCACA[A/G]TCAATTTTAGAACAT | 286053 |
rs77300448 | snp | A/G | 0.030665 | 0.119967 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127543 | AAAGAAAGATTATGT[A/G]ATGTGTTACATGGAA | 286053 |
rs77314492 | snp | C/G/T | 0.0295035 | 0.117819 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278085 | GCTGTGCACATAGCC[C/G/T]GTGAAATATTTGCTG | 286053 |
rs77353541 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242109 | AAACAATAACTGGGG[A/G]GGGAGTTTGAGAACC | 286053 |
rs77361441 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166869 | CGTTCCTCAGGATAG[A/G]TAACTCAAAGTTGGC | 286053 |
rs77367792 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120593 | ATTGGGCAAGCCAGA[A/G]GTTAAGCCTGTTAAC | 286053 |
rs77368857 | snp | C/T | 0.0275645 | 0.114116 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362464 | GCTGGCTCCTCTCCA[C/T]GAGCTTCTTGAGAGC | 286053 |
rs77379298 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338075 | AGAGACCACCCTCCT[C/T]CTAATTCTCATCCCT | 286053 |
rs77407761 | snp | A/G | 0.135484 | 0.22223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205203 | TCACTGACTTCAGGG[A/G]GTCTTCCCTAAGGTA | 286053 |
rs77428913 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138100 | GAAATAAAATGTCAG[G/T]TTTCAAATTCATGAA | 286053 |
rs77436905 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312930 | AGAAGAACTCAGCAA[A/G]TACACAGAAAGCACA | 286053 |
rs77454870 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275442 | CTTCCCTGTACCCTC[A/C]CATGGTATCCAGCAG | 286053 |
rs77488830 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244880 | ACTGCTCAAAGCTTA[A/C]ACTAATAACTACACA | 286053 |
rs77494437 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186313 | GGTTAGCAAAACTTA[C/T]CGTATTTATTATCTG | 286053 |
rs77496010 | snp | A/G | 0.131038 | 0.219882 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185147 | GGTGGGGAGAGGCCA[A/G]GATACAGCTTGCAAT | 286053 |
rs77501282 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278211 | TTTATTTATAAAAAG[A/G]AAAAGGAGTTAAGGG | 286053 |
rs77520935 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312074 | AAAACTCCATCTCAA[A/T]TAAAAAAAAAAAAAA | 286053 |
rs77537002 | snp | C/G/T | 0.00557925 | 0.0525759 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188768 | AGGCCAAAATGTGCA[C/G/T]TTTGCTTCATTTGGG | 286053 |
rs77537711 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244712 | CTGTTAAAAATTCAG[C/T]AAACACTGTCAAAGC | 286053 |
rs77560667 | in-del | -/AAAAGA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327283 | AAAAAAAAAAAAAAA[-/AAAAGA]GAGAGAAACCAAAAT | 286053 |
rs77573294 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111283 | TAACTGACCTTTTAC[A/G]TTTGCAAATGTTAAG | 286053 |
rs77579865 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257095 | TTGAGGCGATCCTGG[C/G]CAACATGGTGAAACG | 286053 |
rs77598495 | in-del | -/GA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272865 | ACACACATATATATA[-/GA]CACACGTATACGTGT | 286053 |
rs77603948 | snp | G/T | 0.0850919 | 0.187897 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106715 | ACAACTTTCATTTTG[G/T]CCGGGTGCTGTGGCT | 286053 |
rs77635110 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294989 | TTTTCTCCTCTGTGA[A/T]CCATCAGTCTGTGTC | 286053 |
rs77664120 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100239 | GTTTCTAGTGAGAGG[A/G]GTCGTAAAAGAGCAT | 286053 |
rs77672845 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153696 | TTGAAAACTCATGTT[C/T]TTTGTCTGTGAAATT | 286053 |
rs77684077 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226627 | TGACTCCTGGAGGAC[A/G]AAACGCCACTTGTCT | 286053 |
rs77696213 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110767 | GGTTGTTGTTGTTTT[G/T]TTTTTTTTTTTTTTT | 286053 |
rs77703655 | snp | A/T | 0.170084 | 0.236883 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258764 | GAGTGGCAATGTGAT[A/T]TGCTTCTTATTTAGT | 286053 |
rs77714350 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292759 | GGAAAATTCAGAAGA[A/G]AAATAAGAGCAAATC | 286053 |
rs77762142 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264879 | ATGCAAATATCTCAT[G/T]TAATCTTCACAACAA | 286053 |
rs77768208 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150426 | TTCTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 286053 |
rs77777704 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340911 | TGCTAATTACATCCC[C/T]TGCATAATTTCTCTG | 286053 |
rs77785791 | snp | A/G | 0.0256215 | 0.110247 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093376 | CTTTAGCATATGGGT[A/G]AGATGTGGGCAGATA | 286053 |
rs77794773 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195623 | ACAGATGTTCATTTA[A/G]TATGCTGGGAATATG | 286053 |
rs77803280 | in-del | -/C | 0.300169 | 0.244914 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230300 | CTTACTGAACTAATA[-/C]CCTATAAAGCCTTAC | 286053 |
rs77807841 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281169 | GAGAAAGTTATAGCT[A/G]GCTCTTTTCCCAACT | 286053 |
rs77818672 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110804 | GGATAATGTTATCTG[A/G]TTTTTTTTTTTAAAT | 286053 |
rs77872709 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365280 | TACCCAGATGAAGCT[C/T]GCTTCTTCCCTTTCG | 286053 |
rs77879746 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241807 | GTAATTGAATTTATT[C/T]CTTCCACAAATATTG | 286053 |
rs77893906 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104006 | CTTTTTTTTTTTTTT[C/T]TCAGCCGGAATTTTG | 286053 |
rs77906557 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208636 | TAGGAGGAGACAAAT[A/G]ATTGAGTGCCAGCGT | 286053 |
rs77934160 | snp | A/C | 0.0551013 | 0.156571 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364305 | TTTCATTGATTAATA[A/C]CCCTCTAATGTAAAA | 286053 |
rs77935065 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351367 | ATAAAAAAAAAAAAA[A/C]ATATTCGAGTTACCT | 286053 |
rs77935838 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344425 | TCATCTATTCCTTCA[A/G]TCTTTTTTCTATATA | 286053 |
rs77980892 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347090 | GCTTGCTATTTGCCA[A/G]GAACCATGCTAAGAA | 286053 |
rs77985299 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234246 | TTGACCAGGCTATAA[A/G]TTCTGATTTTTGTCA | 286053 |
rs77999397 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303308 | TCAAGTTGTGTATTC[A/G]AGACCAAACTGCAGT | 286053 |
rs78014394 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300170 | CAAGGGCTGTGCCTC[C/T]TTTTTTTTTTTTATT | 286053 |
rs78030471 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336120 | AGGAACCATTGATAT[A/G]GCTTTGAAGATAGGA | 286053 |
rs78038926 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237734 | CCAGTCAGTGAGACC[A/G]GGTATCAGAGTCTGC | 286053 |
rs78068134 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180262 | ATTCGTTCTTTAGCC[A/G]TACAGTACTTCTGTT | 286053 |
rs78085118 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288693 | CCTTTAGTTCTATGC[A/G]TGTGTCTTTCTTAAC | 286053 |
rs78119286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299276 | TTTGTCAGTGTGCTC[C/T]GTTTTTAAAAAGAAA | 286053 |
rs78129809 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260515 | CCTCACTTAGTGGAC[A/G]TTGAACCTTTCACTT | 286053 |
rs78155795 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315112 | TCATTGACTAGAATC[C/T]TTTTTTTTTCTTTTT | 286053 |
rs78158131 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331601 | ATCTTTTTTTTTTTA[A/C]CAAAATAACCAGATT | 286053 |
rs78162782 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196424 | TGTTCTTATTGTTCA[A/G]TTCCCTCATATGAGT | 286053 |
rs78163516 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204726 | CCATTCAATAAGATA[C/T]GCTGTCTAGTCCCAT | 286053 |
rs78187665 | snp | C/T | 0.204803 | 0.245881 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297151 | ACCCATTTTTAACAA[C/T]CTGTATTTCATATTT | 286053 |
rs78195807 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196544 | GAATTCTATGCAGCC[A/G]TAAAAAGGGATGAGT | 286053 |
rs78197500 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140663 | CAAAAAAAAAAACAT[A/G]TGAGATTTAAGCCTC | 286053 |
rs78209476 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191419 | TCTTGGAAAAAAAAA[A/T]TTGACTTTTAATAGG | 286053 |
rs78214529 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131805 | TAATTCTGATACATC[C/G]TGAAGTTTGAGAGCC | 286053 |
rs78215850 | snp | A/C/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277524 | TCTTTTTTTTTTTTT[A/C/G]GAGATGAAGTCTCGC | 286053 |
rs78218036 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091938 | GGGGTGCCACCAGAC[G/T]GAGACAGCTTGGACT | 286053 |
rs78221197 | snp | A/C | 0.0836354 | 0.186609 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193194 | TTACAAGTAGGTTAA[A/C]TACACATTTATGTAA | 286053 |
rs78258496 | snp | C/T | 0.151668 | 0.229849 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328909 | TGTTTCAGTGAGACC[C/T]GAAGTCAGAACTCCT | 286053 |
rs78290275 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364304 | ATTTCATTGATTAAT[A/G]CCCCTCTAATGTAAA | 286053 |
rs78310046 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150210 | AGGGAGAGATTACTT[C/T]TGGTTCATCTTTATA | 286053 |
rs78316057 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351366 | CATAAAAAAAAAAAA[A/C]CATATTCGAGTTACC | 286053 |
rs78327482 | in-del | -/AA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263769 | AAAAACAAAAAAAAA[-/AA]GAAGAGGCCTGATAT | 286053 |
rs78341100 | snp | A/T | 0.0584853 | 0.160693 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115739 | CTCAATAAAAAAAAA[A/T]AATAATAAATAAATA | 286053 |
rs78345378 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249186 | AAAAAAAAAAAAAAA[A/T]AGGCAGAGCCATGAG | 286053 |
rs78347313 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291658 | TGATCTTAGTGATGG[A/T]AAAGATAGAGGAGAA | 286053 |
rs78348516 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176121 | TAAAATGAGCAATTC[A/G]TTGAAGAGTCTGTGG | 286053 |
rs78349818 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131974 | TAACAACATTGTAAA[A/G]GCTTTGCTTTGGGGG | 286053 |
rs78361819 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268066 | AAACCCTCATCTCTA[A/T]TTAAAAAAAAAAAAA | 286053 |
rs78373908 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233608 | TCCGAAATGAAATGA[A/T]TGTAAATGCACTTTT | 286053 |
rs78388974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257912 | GCCAAGGCAATGAAG[A/T]GTAGCTAGAGAAGAA | 286053 |
rs78390266 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321268 | ACACAGGATTTTTTT[C/T]CTTAATATTCTAACC | 286053 |
rs78392402 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149110 | CTGAGCCTTTTCTCA[C/T]GCACCATTTTGTTAA | 286053 |
rs78398259 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115742 | AATAAAAAAAAATAA[A/T]AATAAATAAATAAAT | 286053 |
rs78404943 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231483 | ACCTCTTTAATGCCT[G/T]TCTTTGTTCCCTGGA | 286053 |
rs78409348 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218430 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT | 286053 |
rs78429696 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121843 | ACCTTGAGGTTGACC[A/G]AGGACTATATACTGT | 286053 |
rs78430007 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242784 | CACTCACAGCACAAA[C/T]GCATACCCATGCGAT | 286053 |
rs78435068 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211628 | CTGAGTCAAAGGAGA[C/T]GTGAATTTTTAGATT | 286053 |
rs78469918 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346157 | AGCGAAACTCCGTCT[A/C]AAAAAAAAAAAAGAA | 286053 |
rs78472454 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095419 | CACAGGGAGATGGTC[A/G]TCTCTACTAAAAATT | 286053 |
rs78473263 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232506 | TATTTTAAAGGTGAC[A/G]CATTTATTACCATAC | 286053 |
rs78493848 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358332 | AGCTAGACTCTGTCT[A/C]AAAAAAAAAAAAAGG | 286053 |
rs78503936 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321158 | GATTTGGGCAAGGAC[A/G]TAGATCCAAACCATA | 286053 |
rs78514737 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336112 | TGGTAGAAAGGAACC[A/T]TTGATATGGCTTTGA | 286053 |
rs78515355 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257121 | TTTTTTTGCATTTTT[A/G]GTAGAGATGGGGTTT | 286053 |
rs78517513 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324942 | TCAGTTGTGTTGGAG[-/T]TGGGGAGTAGAAGCC | 286053 |
rs78530809 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315546 | TTCAACTAGCTAATT[A/C]ATGAAAAGTGTTTAT | 286053 |
rs78545183 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271656 | GACCTTTGGAAGAGT[A/G]CTGAATAGGTATGAA | 286053 |
rs78561824 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335469 | TAAGCCCCTGCTGGA[G/T]CCTTCCAAATATGTC | 286053 |
rs78564432 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283876 | TGACTCAAGTAGGCC[A/G]GGCGCAGTGGCTCAC | 286053 |
rs78603397 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127390 | TCTTCTTAATAGGAA[A/G]AAATGATGTTTATGA | 286053 |
rs78624553 | snp | G/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192215 | AAATAATTATCTTGT[G/T]GAGTTATAATTCCTG | 286053 |
rs78655437 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295913 | ATAACCGTTGCCCCT[A/G]CTGAAGATCTTAAAC | 286053 |
rs78655708 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160214 | TAATTTAGGTCACAG[A/G]GTTTCATTAAGGATG | 286053 |
rs78656204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345270 | GCTTTTGTACAGAAG[C/T]GGAACAGAGAATGAA | 286053 |
rs78663786 | snp | G/T | 0.121717 | 0.214577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315213 | AAGTAGATAGGTAAG[G/T]AATGTCAGGCCCCAA | 286053 |
rs78664279 | snp | A/G | 0.0644444 | 0.167538 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319405 | AAAACTGACCTAGAA[A/G]TGACACAGATATAAA | 286053 |
rs78666438 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132199 | AACTCCTGGGCTCAA[-/G]CCATTCTTCCACCTC | 286053 |
rs78688900 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315816 | TTTTTTCCCTCTCTT[C/T]TTTAAAGTCAGGGTT | 286053 |
rs78690636 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166765 | CCAGCTATGGAAGAC[C/T]GGTCTTCCTGGTTTA | 286053 |
rs78718861 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176107 | AAGTGATTTTGAGCT[A/G]AAATGAGCAATTCGT | 286053 |
rs78733198 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238622 | CACCAGCTTCCAGCC[A/G]GAATAATTGATAACT | 286053 |
rs78737925 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193452 | GCTAATAAACATATG[A/G]AAAATATTTTTTAAA | 286053 |
rs78740438 | snp | A/T | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362909 | AGCATGCTCTCATGC[A/T]CTGACTAAAACCATG | 286053 |
rs78745155 | snp | A/G | 0.122411 | 0.214991 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326382 | TATCTCTTTGAGTAA[A/G]AATAGGCATTATATA | 286053 |
rs78752407 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234011 | GAAACCCTGTCTCTA[A/C]TAAAAAAAAAAAAAA | 286053 |
rs78755278 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280486 | AACTGCTTATTTGAA[A/G]CAATAAAGCTGAGTT | 286053 |
rs78757514 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094834 | GAGAGCAGTCCCTGG[C/T]GTCTCTTCCTTTTCT | 286053 |
rs78768275 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195473 | CATAAGCACATACAT[A/T]TAAGTCACTTAGTAA | 286053 |
rs78781467 | in-del | -/CGG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242107 | TAAACAATAACTGGG[-/CGG]GGGGGAGTTTGAGAA | 286053 |
rs78826310 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189622 | AACATAGTTAAGGCA[A/G]TCTGATGATAAAAAT | 286053 |
rs78826883 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212637 | TAGTTTCTAAATTAG[A/G]GATGGTTGATCAGAT | 286053 |
rs78850745 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188674 | CACTTTAATGAGAGA[C/T]GGCAGCCGTTTAATT | 286053 |
rs78856090 | snp | A/G | 0.172351 | 0.237636 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267894 | TGGTGGAATTAGGAA[A/G]GAAAGAGAAAGCAGA | 286053 |
rs78862184 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202799 | GCATAAGCAATGTTT[G/T]AATAATTTTGTTAAT | 286053 |
rs78863581 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172201 | GTTGCCAGCCACCCT[C/T]TGTGCTGCACCTCCC | 286053 |
rs78878916 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179862 | AGGTTGACTGTGTTA[C/G]AGACTTTGTTGGAAA | 286053 |
rs78900023 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303527 | CTGCTTATTTTGTGC[A/G]AAGTATAATACTGGG | 286053 |
rs78916590 | snp | A/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195288 | GTAAGTCCACAGGCA[A/T]TTTTTTTTAATGTTC | 286053 |
rs78917784 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112118 | AAGAAGCCAATGTTT[G/T]TATGCTTATACAGCT | 286053 |
rs78921697 | snp | G/T | 0.121022 | 0.21416 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110343 | ATATATTGCTTTTCT[G/T]TCTGTGATTTCGGAG | 286053 |
rs78973660 | snp | A/G | 0.122411 | 0.214991 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338645 | AGCTAACATCATGCA[A/G]GATGAAAGCCTGGCA | 286053 |
rs78981325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233326 | CATTTTTGTGATTAA[A/T]TTTTATTGATCTTTT | 286053 |
rs78981563 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264048 | ATCTTCAGATTTCCC[A/G]TGTCTGGCACATAAC | 286053 |
rs78988264 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234701 | GTTATAAACTCTTAA[C/T]GTTGATGATGTTCCA | 286053 |
rs78992933 | snp | A/G | 0.233818 | 0.249476 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268694 | GATGCACATACACCC[A/G]TTGCCTAGAAAGAGA | 286053 |
rs79035150 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321765 | TGTATAATTCACCAT[A/G]TTAACAGAGCAAAAA | 286053 |
rs79067069 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266109 | TTTTTTTTTTTTTTT[G/T]GAGATGGAGTTTTGC | 286053 |
rs79067659 | in-del | -/CTC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190177 | GTATTTGCCTCTCTC[-/CTC]TTTCCTCCTCTCTGA | 286053 |
rs79069463 | snp | G/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232472 | ATAAGCTTCAGGTGC[G/T]TTTAGAATCTTAACT | 286053 |
rs79073869 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344232 | AAATCCATCCACCCT[C/T]ATTGCCGTCAGTCCT | 286053 |
rs79078490 | snp | C/G | 0.0603597 | 0.1629 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354765 | GGAGGCAGAATCCCT[C/G]TGTTGCAATTAATTC | 286053 |
rs79086755 | snp | A/G | 0.101301 | 0.200969 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323654 | TAAACTTTGAACCAT[A/G]TCTCACACCATATGT | 286053 |
rs79092686 | snp | A/G | 0.029116 | 0.117091 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349639 | AGCCTAATTGAAAAA[A/G]TACATAGCAATCAAA | 286053 |
rs79096821 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241068 | TGGAATATTGGCACT[A/G]TTCTTACGGGTTGAA | 286053 |
rs79113303 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126372 | TGAGACTCTGTTTCA[A/C]AAAAAAAAAAACGAG | 286053 |
rs79120248 | snp | A/G | 0.081446 | 0.184634 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204038 | CTGTCTTAATCTGTT[A/G]TATCCCTAGTGCCTA | 286053 |
rs79125348 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177226 | TAGTTAAGTCTTCAC[A/G]GCACTGAAGTGGGTG | 286053 |
rs79137969 | snp | A/T | 0.0566069 | 0.158427 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265048 | ATCAAGTAATATTTT[A/T]TGTAGTATCTTAAAA | 286053 |
rs79143428 | snp | A/C | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362908 | CAGCATGCTCTCATG[A/C]ACTGACTAAAACCAT | 286053 |
rs79153600 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262655 | ATGCTTTTAGCTCCA[C/T]AATCTGGTGTCATGG | 286053 |
rs79171288 | snp | C/G | 0.0637235 | 0.166737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158950 | CTACAGTTTCACTTT[C/G]CACTGTTTCAGTTAT | 286053 |
rs79173164 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180200 | TTCTTGAGATATAAG[A/G]CACTATTATATTGCC | 286053 |
rs79186771 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366297 | GGTAATCCCAGCACT[G/T]TGGGAGGCCGAGGCG | 286053 |
rs79191171 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201503 | TTTGCTGTTCTACAG[C/T]CACCGCTGGTGAAAC | 286053 |
rs79202834 | snp | C/G | 0.167158 | 0.235875 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254504 | TTGAACAAGTAAATA[C/G]CATGTACTTCACCAT | 286053 |
rs79236813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291563 | CACAATGGGAAAGAC[A/G]TGTTCTCCAAAGGAG | 286053 |
rs79285705 | in-del | -/AAAAAAAGA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256953 | AAAAAAAAAAAAAAA[-/AAAAAAAGA]GGGCTGAAGGTGAAA | 286053 |
rs79291104 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224651 | TTTCTATTCTGTTCC[A/G]GTGGTTGGTGAGTGG | 286053 |
rs79309462 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257122 | TTTTTTTTGCATTTT[A/T]AGTAGAGATGGGGTT | 286053 |
rs79316374 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143389 | TACGTCCCATTTATT[C/T]TAAGAAATTTAAAAT | 286053 |
rs79331579 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355701 | CGAGACTCCATCTCA[A/C]AAAAAAAAAAAAAAA | 286053 |
rs79357341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290002 | TTTCACGGAGTTTAA[A/G]GAATGTTGGTCTTTG | 286053 |
rs79358795 | snp | G/T | 0.0539704 | 0.155153 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349154 | GAGTCCACAGGTGGG[G/T]TTACTGGTAGCCCCA | 286053 |
rs79385103 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273069 | ACCTGACAGTTACTG[C/G]TTCATAAATGGTTGC | 286053 |
rs79393465 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130790 | GCTAATCTAGTGCTG[C/T]GTGGTTAAATTCTTT | 286053 |
rs79398367 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280854 | TCTCATTATAAACTG[G/T]TGTAGTTAATCTGTA | 286053 |
rs79405146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205283 | GAGAAGAGTATCTAA[G/T]TACAAAGATTAGGAA | 286053 |
rs79427432 | snp | C/G | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362907 | TCAGCATGCTCTCAT[C/G]CACTGACTAAAACCA | 286053 |
rs79428448 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149807 | TGATTGTTATTCTTA[A/G]TGGCTTGTTTTCTTG | 286053 |
rs79429017 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115949 | CTCACTCCACAGAAG[A/G]GGAAATTAGGCTCAT | 286053 |
rs79438574 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180732 | AAACTGGGGGGAGGA[C/G]ATCAAGATTAGATTA | 286053 |
rs79452480 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194327 | ATTTTTCCAGAATGT[C/T]GTATAGGTAGAATTG | 286053 |
rs79477672 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312077 | ACTCCATCTCAATTA[A/T]AAAAAAAAAAAAAAA | 286053 |
rs79490351 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253520 | TTTGACTTTCCATTT[G/T]CCACTTTAACTGTGA | 286053 |
rs79490897 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196447 | CTATGAGTGAGAACA[C/T]GCGGTGTTTGGTTTC | 286053 |
rs79495035 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312251 | AACTGAAATAGAAAC[A/G]TTAACATTTCAGATG | 286053 |
rs79510006 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125363825 | CCTAATGCAAAGCCA[A/G]ATCATCAAAATGATG | 286053 |
rs79536300 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357355 | CCCTGAAAGAAACAC[G/T]ATTCACTTCACAGAG | 286053 |
rs79538239 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116840 | GGGCCAATGGCCATA[A/C]TGAAGATATATCTCT | 286053 |
rs79545614 | snp | A/G | 0.16976 | 0.236773 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255576 | GAGGAAGGAAACAAC[A/G]TGGTGTGCAGAAGGA | 286053 |
rs79564965 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218429 | GTTTTTTTTTTTTTT[G/T]GAGACAGAGTCTTGC | 286053 |
rs79572766 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126906 | TCACTTGGCACACAG[C/T]GTTCTTATTTTATCT | 286053 |
rs79604538 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112247 | AAAAGTAAAAGGCAA[C/T]GCCTACACCAGGATG | 286053 |
rs79625464 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158236 | AGCCTTAAAGATGTT[C/T]CCATGTTGAAGGTCA | 286053 |
rs79634415 | snp | C/T | 0.205417 | 0.245993 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332551 | CAGTAAATAATAGTC[C/T]TCATATTACAAAACA | 286053 |
rs79634595 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147911 | CTACTTGACATGGAC[A/G]TTCTCATGACCTGTC | 286053 |
rs79670249 | snp | A/G | 0.0126979 | 0.078662 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092793 | ACCGGGAAGAAAAAG[A/G]TCAGTGTTATTACCT | 286053 |
rs79682945 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229237 | AAAGAAAAGAGAGAT[A/G]CAAGAGACTGGGAGA | 286053 |
rs79690390 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331602 | TCTTTTTTTTTTTAA[C/T]AAAATAACCAGATTC | 286053 |
rs79692332 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317003 | ATGTTGCCCAGACTG[A/G]TCTTGGACTTCTCAT | 286053 |
rs79734530 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273201 | ACAGCCTATTAAAGA[C/T]GCCAGTGAGACATTT | 286053 |
rs79737036 | snp | G/T | 0.134802 | 0.221877 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259113 | CTCCATATTGGTCAG[G/T]CTGGTCTTGAACTCC | 286053 |
rs79761457 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131247 | ACATACTGCAATCTC[C/T]TTTTGAAAATATATA | 286053 |
rs79767000 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312076 | AACTCCATCTCAATT[A/T]AAAAAAAAAAAAAAA | 286053 |
rs79769550 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218173 | AGCTGCATGCATCCC[A/G]CTTTAGAAACCTGTA | 286053 |
rs79791567 | in-del | -/GAG | 0.135484 | 0.22223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175729 | TAATGATAATTGGAA[-/GAG]GAGGAGACTTTGACT | 286053 |
rs79819831 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147104 | AAGTGTTGTACAGCA[A/G]TGCTTTTCTCTCTGG | 286053 |
rs79823717 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310604 | AGCCCCCTTTTTTTT[G/T]GTCTTCTGCATACCT | 286053 |
rs79853783 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315121 | AGAATCTTTTTTTTT[C/T]CTTTTTTCTTTTCAT | 286053 |
rs79862437 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366524 | CAGACTCCGTCTCAG[A/G]AAAAAAAAAGAAAGT | 286053 |
rs79866116 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154726 | AGTCATAAGACCAAC[A/G]TGTCATAAAAGTGTT | 286053 |
rs79867381 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229197 | CATGGAGAACCTGAA[A/C]TACTGCAGTGATAAT | 286053 |
rs79877675 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160607 | CTTCCCTGATAGTCA[C/G]CCTCCCTATGTCTAT | 286053 |
rs79883754 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317667 | ACTCAGTATAGCAAC[A/G]CTATTATCTGATTCC | 286053 |
rs79898144 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271496 | GGTATTAAGGGTACA[C/T]AGGACTGATGTCAGC | 286053 |
rs79912357 | snp | A/G | 0.134119 | 0.221521 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105260 | TCTTTTTAGTGGGTG[A/G]CCTCCAAATGTTTTA | 286053 |
rs79952672 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360527 | CCAATGAGAGGATCA[A/G]TCAGCGGAAGAAGAC | 286053 |
rs79958100 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202627 | TATTATATGTGAAAA[A/G]TGTTTTATAAACTGT | 286053 |
rs79961940 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366296 | CGGTAATCCCAGCAC[A/T]TTGGGAGGCCGAGGC | 286053 |
rs80000344 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158215 | GTCGAACTCCCTTCC[A/G]AAATGAGCCTTAAAG | 286053 |
rs80007251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121941 | AATTATTTACTCCTT[A/G]CATATTCTCACCCAT | 286053 |
rs80009601 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212231 | TAGCAAGGCGAACAC[A/G]TATTCATTTAAAGGT | 286053 |
rs80035704 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136299 | GGAAAAGGAAATGAC[A/G]AAGGAAACAAATCAA | 286053 |
rs80039535 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111328 | AATAGTTTTAAATCC[A/G]GGTGCTTTGGGGGTA | 286053 |
rs80069131 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243496 | TTGCAAAAATAATAA[A/T]TTTTTAAAAAAAAAA | 286053 |
rs80069993 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096672 | ATACGGAGTCTTTTT[G/T]TGATCTCAGCTCACT | 286053 |
rs80072448 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251998 | CTTTGGTGATAAACC[A/G]TTGAAATATGGTCTG | 286053 |
rs80080276 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219745 | AATTAATAAAATGTC[A/G]CTGAAGTTTTGTTTT | 286053 |
rs80081684 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271634 | GCTTTTGGCCCCTTA[A/C]AACTGAGACCTTTGG | 286053 |
rs80083255 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313789 | AAAAAAGAAACAGAA[C/T]TTTACTTTTCTTCTC | 286053 |
rs80086773 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152705 | AAGAACGTTATGTTG[A/T]TTTTTTTTCCCTATT | 286053 |
rs80088574 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226347 | GTTATCAGATGATAA[A/G]TTCTAATCATGGGAC | 286053 |
rs80099114 | snp | C/T | 0.029116 | 0.117091 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292202 | CTAGCAATATGTAGA[C/T]TCAAGAAGCTATGGG | 286053 |
rs80100810 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196547 | ACGGAATACTGTGCA[A/G]CCATAAAAAAATGAT | 286053 |
rs80121459 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186975 | ACAAAGAATTTTATC[C/G]TTTAGATACCCAGTG | 286053 |
rs80130052 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203572 | TCATAGCAAAATTGA[A/G]CATAAGATACAGAGA | 286053 |
rs80133686 | snp | A/T | 0.277778 | 0.248452 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196425 | GTTCTCATTGTTCAA[A/T]TCCTACCTATGAGTG | 286053 |
rs80138136 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315799 | CCTTTGTTGGTACCC[G/T]TTTTTTTCCCTCTCT | 286053 |
rs80202857 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176373 | GGATATTTTCTTTTG[A/G]TTGTTTCTTAACTCT | 286053 |
rs80223514 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234032 | AAAAAAAAAAAAAAA[A/T]AATACAAAAAATTAG | 286053 |
rs80240786 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104008 | TTTTTTTTTTTTTTT[C/T]AGCCGGAATTTTGCT | 286053 |
rs80265276 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243587 | TCAAGAATCATATCT[C/T]AATGTTATTAAATAG | 286053 |
rs80266418 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347757 | GATTGGCTATGGAGA[C/T]TGTGTTGGGTGGATT | 286053 |
rs80282374 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277523 | TTCTTTTTTTTTTTT[C/T]CGAGATGAAGTCTCG | 286053 |
rs80291780 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106548 | CCGGGCGTGGTGGTG[C/T]GCACCTGTAATCCGA | 286053 |
rs80343391 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349702 | TGGTAGCCAAATTTG[A/G/T]GATGCCTGAAGACAG | 286053 |
rs80345848 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231988 | GACTCCTCTGAACCT[C/T]GTGTTTCTTTTTCAT | 286053 |
rs111243411 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346153 | CAAGAGCGAAACTCC[A/G]TCTCAAAAAAAAAAA | 286053 |
rs111266769 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320313 | AAGGAAGGAAGGGAA[A/G]GGAAGGAAGGGAAGG | 286053 |
rs111270316 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118364 | CCAGCCTGGGTGACA[A/G]AGTGAGACTGTCTTA | 286053 |
rs111285524 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108147 | GGACCCCCTGAAATG[G/T]CTCAGAAGACCACAC | 286053 |
rs111286245 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222853 | GGATTGCTTGAGCTC[C/T]GGAGTTCAAGACCAG | 286053 |
rs111293055 | snp | A/G | 0.196771 | 0.244268 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271946 | GGAAAACCCAGAGAT[A/G]TTCGGTGACTTGGCC | 286053 |
rs111308468 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184877 | TGAGATATGTTCTGG[C/T]GGCAAGGAATTACAA | 286053 |
rs111310247 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129179 | GGTGGGGAGGGAATA[C/G]GTGAAATGACAAGAA | 286053 |
rs111315029 | in-del | -/GATGACCTCTGTA | 0.030665 | 0.119967 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206871 | GGAGCTCTAGGAGTG[-/GATGACCTCTGTA]AAGGGAAGAGAGAGC | 286053 |
rs111322259 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103582 | TTAATTCCTCTGCTC[C/T]CCTCTCCTTCTGTGT | 286053 |
rs111326288 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216636 | CGAGGCTGTGTGTCA[A/C]AAAAAAAAAAAAAAT | 286053 |
rs111332781 | snp | C/T | 0.444444 | 0.157135 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269541 | TTTATTTCCTGTGCT[C/T]ATCATGGCTTGGATG | 286053 |
rs111352232 | in-del | -/CCCG | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196391 | CAGTGTGTGATGTTC[-/CCCG]CCCGCCCTGTGTCCA | 286053 |
rs111355815 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309249 | GCAAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs111359532 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212324 | TGCAGAGCTGGGTGA[G/T]TTAGGTGGGAAGAAT | 286053 |
rs111359849 | snp | A/C | 0.5 | 0 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125357771 | CTATGAAGAGGACGC[A/C]ATTGTTCGCATGATT | 286053 |
rs111366359 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261856 | AATCCCAGCACTTTG[A/G]GAGGCCAGCATGGTC | 286053 |
rs111378826 | in-del | -/C | 0 | 0 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196342 | TTCTCCCAATGCTAT[-/C]CCCTCCCCCTGCCCC | 286053 |
rs111383324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267324 | GGGTACCTTTTCTAA[A/G]TATATGTTCTCTTTA | 286053 |
rs111387019 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263388 | CTTAGGAAGAAACTA[G/T]AAGGTTACTTCTAGC | 286053 |
rs111389551 | snp | C/G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295604 | CTGAGAGGGACAAAG[C/G/T]GGGTAAAGAACTGAG | 286053 |
rs111391574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164147 | AATTCTGAAACCAAC[A/G]TTCTTTCCCTCAGTG | 286053 |
rs111403413 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345122 | TTTCTGGCCAGGGAA[C/T]AGAATCAGAGGTGAT | 286053 |
rs111408884 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316919 | GAGTAGCTGGCACTA[C/T]AGGCGTGTGCCACCA | 286053 |
rs111416366 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266263 | CGCCCGGCTAATTTT[C/G]TGTTTTTAGTAGAGA | 286053 |
rs111426462 | in-del | -/A | 0 | 0 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196192 | GCAGCCCTGGATAAC[-/A]TTTTTTTTTTCTTTT | 286053 |
rs111463968 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196510 | TCCAGCTTCATCCAT[-/A]GTCCCTAAAATGAAC | 286053 |
rs111465857 | in-del | -/A | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250155 | CCACCATGCCTGGCT[-/A]AATTTTTGTATTTTT | 286053 |
rs111470319 | snp | C/T | 0.232943 | 0.249417 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286585 | CCCAAAGTGCTGGGA[C/T]TACAGGCATGAGCCA | 286053 |
rs111506438 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094663 | AAAATACCATAGACT[A/G]GGTGGCTTAAACAAC | 286053 |
rs111518702 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326816 | CAAAAATTAGCCGGT[C/T]GTGGTGGCGGGCACT | 286053 |
rs111524934 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135630 | TTTCTTTGCATGTGG[A/G]TAGCCAATTGTCCTA | 286053 |
rs111527821 | snp | G/T | 0.0832709 | 0.186283 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199858 | TATGAATCTGGGTGC[G/T]CCTGTGTTGGGTGCA | 286053 |
rs111555826 | in-del | -/CA | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196641 | TATTGTGGCACTATT[-/CA]CACAATAGCAAAGAC | 286053 |
rs111570662 | snp | C/T | 0.166506 | 0.235645 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298089 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 286053 |
rs111572273 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193713 | AAAACAAAACAAAAA[C/G]CGTATTTCTTCTTCT | 286053 |
rs111596317 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256960 | AAAAAAAAAAAAAAA[A/G]AGGGCTGAAGGTGAA | 286053 |
rs111602506 | snp | A/G | 0.145305 | 0.227022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326859 | TACTCAGGAGACTGA[A/G]TCAGGAGAATCACTT | 286053 |
rs111635109 | in-del | -/A | 0.0356815 | 0.128715 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150117 | TGGCCAGTTTTTCTG[-/A]AAACAAGTTTGTTTT | 286053 |
rs111675189 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218574 | CTGCCACCATGCCTA[A/G]CTAATTTTTGTATTT | 286053 |
rs111675971 | snp | C/T | 0.139225 | 0.224118 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198616 | TGAGGATTTTCACAT[C/T]GATGTTCATCAGAGA | 286053 |
rs111687639 | snp | A/T | 0.444444 | 0.157135 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270474 | TGTCTCAAAGCAAAA[A/T]ACAAAACAAGACGAA | 286053 |
rs111703377 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298650 | TGAACGTGACCAGTG[A/G]TTCTTAACAGGGATT | 286053 |
rs111710160 | in-del | -/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196457 | AACATGCAGTGTTTG[-/G]TTTTTTTTGTCCTTC | 286053 |
rs111743706 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279002 | ATATTTTGTGTTTGT[A/G]TAATCATTATATTAG | 286053 |
rs111748749 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289460 | CCCACCTCAGAATGG[G/T]TTAGAGGCCTTTCAT | 286053 |
rs111749670 | in-del | -/TAAAA | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325294 | AAACCCCGTTTCTAT[-/TAAAA]TAAAATAAAATAAAA | 286053 |
rs111752833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196629 | ATTCACAATAGCAAA[A/G]ACTTGGAACCAACCC | 286053 |
rs111758825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112224 | TTAATTATGCTGTAT[A/G]TAGTACTAAAAGTAA | 286053 |
rs111774742 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116679 | CTTAACCTACTTATG[C/T]CATTAGCAGTAATGT | 286053 |
rs111793039 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166252 | TTACTGTAGTCATAC[G/T]AAATAGGTTTTGTTG | 286053 |
rs111793678 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157796 | TTGGGTTTTAATCAG[A/G]CTTATAAAACTGTTA | 286053 |
rs111794451 | snp | C/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328980 | CTGTCCCATCAGACA[C/G]TCTGCAGACCAAGGA | 286053 |
rs111805361 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146748 | CTGGGGCCTGTTGTG[A/G]GGTGGGGAGAGTGGG | 286053 |
rs111815933 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111329 | ATAGTTTTAAATCCG[A/G]GTGCTTTGGGGGTAA | 286053 |
rs111831505 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316629 | TTTATTTCCTTCTTT[C/T]CTTTCTTTATTTCCT | 286053 |
rs111835213 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139749 | TGAGATTTGGGTGAG[A/G]ACACAGCCAAACTAT | 286053 |
rs111835620 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325821 | ACTGGGCATGGTGGC[A/G]GGCACCTGTCATCCC | 286053 |
rs111860572 | snp | C/G | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093008 | CTAAATGTCCCCTTG[C/G]GAGAGGGGTAAAATC | 286053 |
rs111864360 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128424 | TTGATGAAACTTGAT[G/T]GTTTATTGAATATGG | 286053 |
rs111875207 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196524 | ATGTCCCTGCAGAGG[A/G]CATGAACTCATCCCT | 286053 |
rs111880142 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159079 | CCTTGTGCCTTGCTG[C/T]TCTGTCCTGTCTTCA | 286053 |
rs111884398 | snp | C/T | 0.10237 | 0.201756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316779 | CTTCCTTCTCTCTCT[C/T]TCTTTCTTTCTTTCT | 286053 |
rs111888103 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151797 | GTCACAGGAACAACA[C/T]ATAAGGCAGTTAAGG | 286053 |
rs111893026 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237819 | GATTCCCCAGGTGAT[A/G]CCCATCTGCATCGTT | 286053 |
rs111893973 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310227 | AAATAAGGAAAATAC[A/G]TAACTCAGACTAGAG | 286053 |
rs111895533 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239472 | AAATTAGCTGGGCAT[A/G]GTGGTGCACGCCTGT | 286053 |
rs111919474 | snp | A/G | 0.084728 | 0.187577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218512 | CGCATCTTGGGTTCA[A/G]GCAATTCTCATGCCT | 286053 |
rs111920180 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271073 | AAGACCAGCCTGAAC[A/G]ACATAGTGAGACCCC | 286053 |
rs111925223 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346113 | AGTGAGCCAAGATCG[C/T]ACCATTGCACTCCAG | 286053 |
rs111925668 | in-del | -/TT | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243534 | AATTTCTAATGTGTA[-/TT]GTCATTGAAAATTGA | 286053 |
rs111930782 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115739 | CTCAATAAAAAAAAA[-/T]AATAATAAATAAATA | 286053 |
rs111953467 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285945 | CAGGTTTGACCTGAC[C/T]AAAACTTGAGCCCTT | 286053 |
rs111984938 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279696 | TTTATTAAAATAATC[A/G]AGTGTGTCATCTTGA | 286053 |
rs112020421 | snp | C/T | 0.18325 | 0.240924 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106811 | GACCAGCCTGGCTAA[C/T]ATGACGAAAACCTGT | 286053 |
rs112058652 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309332 | TTTAATCAGTGTATA[A/G]AAATTCATTAAGCAC | 286053 |
rs112058855 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133461 | GTCTTTAAATTCAGC[C/T]GGGTGTGGTGGCTCA | 286053 |
rs112088226 | snp | A/C | 0.444444 | 0.157135 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171250 | TTCTACTCAAGTAGA[A/C]TACAAACTCCACAAG | 286053 |
rs112102889 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191630 | AGATCTCCATGGTTT[G/T]GGCAATTCATTTAGA | 286053 |
rs112103504 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103449 | AATTTGTGATGTGCC[A/G]TGGTGTGATTTTTTT | 286053 |
rs112105091 | in-del | -/AT | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146798 | TATACCTAATGTTAA[-/AT]GACGAGTTAATGGGT | 286053 |
rs112113325 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203717 | GTCTTGGAGGTGAGA[A/G]GAAAAGGAGACTAGT | 286053 |
rs112120116 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344619 | GTGGTGGCATGCACC[C/T]GTAATCCCAGCTACT | 286053 |
rs112124235 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126328 | GTGAGCCGAGATTGC[A/G]CCATAGCACTCCAGC | 286053 |
rs112136969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153115 | TTCAGGACATTGAGT[C/T]ACTCATTTAAAAAAA | 286053 |
rs112173997 | snp | A/T | 0.0494327 | 0.149241 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198387 | AGTTTATTGAGAGTT[A/T]TTAGCATGAAAGGCT | 286053 |
rs112186439 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355219 | TCAGTTCTATGGAAC[C/T]GAAAGGTATGCCACA | 286053 |
rs112193529 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223423 | ATATCTTGACTATTG[C/T]GAATAATGCTGCAGT | 286053 |
rs112239760 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270896 | AACATAGTGAGACAC[C/T]ATCTCTTAGAAAAAA | 286053 |
rs112240606 | snp | C/G | 0.0494327 | 0.149241 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213681 | TTTCTCTCTTTCTCT[C/G]TCTCTTTCTTTCTCT | 286053 |
rs112258466 | snp | A/G | 0.135825 | 0.222405 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199626 | TAGAATAAGTGTGAT[A/G]TGGTGCTGAGAAGAA | 286053 |
rs112275129 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281547 | CGGGTTCAACCGATT[A/C]TCTTGCCTCAGCCTC | 286053 |
rs112276872 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290238 | GAATATGTTAAAATC[A/G]TATTAAGTAGAAATG | 286053 |
rs112279172 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210278 | ATGTGTTAGCTATTC[A/G]TTACTGTCATTATTA | 286053 |
rs112288723 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281923 | TCCAATATACTTCCT[A/G]ATCTCCCTCCATGCT | 286053 |
rs112308316 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093929 | AGCCTTCCGAGGGTC[C/T]AGGACAATAGGTGCA | 286053 |
rs112321099 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365583 | ATCCAAGTCCAGGCA[C/T]GGTGGCTCATGCCTG | 286053 |
rs112325176 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326836 | TGGCGGGCACTTGTA[A/C]TCCCAACTACTCAGG | 286053 |
rs112332324 | in-del | -/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320303 | GAAGGAAGGAAGGAA[-/G]GGAAGGGAAGGGAAG | 286053 |
rs112354187 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365780 | GAGAATTGCTTGAAC[C/T]CAGGAGGCGGAAGTT | 286053 |
rs112368329 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360533 | AGAGGATCAATCAGC[A/G]GAAGAAGACCCCTAA | 286053 |
rs112376378 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345138 | AGAATCAGAGGTGAT[C/T]GGGGGCGTAGATGGT | 286053 |
rs112379788 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111645 | TCTCTACCAAAAATA[C/G]AAAAATTAGCTGGGT | 286053 |
rs112409727 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345777 | GTCTGGGATGGATAT[A/G]GGGGATAGGATTGAA | 286053 |
rs112410667 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345797 | ATAGGATTGAAGTGA[A/G]TAGAGTAGGAGATGA | 286053 |
rs112419942 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097330 | TTTCCATGATGACCA[C/G]TAGACCCAACTGGAG | 286053 |
rs112455547 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168708 | CCTCACCTCCTAATA[C/G]CATCACCTTAAGGGT | 286053 |
rs112461657 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230609 | CTTCAGTGAATTTTT[A/G]CTCAACACCAGATGA | 286053 |
rs112463841 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343796 | GTCAGGAGATTGAGA[A/C]CATCCTGGCTAATTC | 286053 |
rs112480337 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196429 | TTCTCACCCACAGGT[A/G]GAAATTGAGCAATGA | 286053 |
rs112484702 | snp | C/T | 0.197703 | 0.244469 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270526 | CTGAAGGCAATGGCA[C/T]GTGTTGAATTGCTTT | 286053 |
rs112485487 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111279 | TGAATAACTGACCTT[C/T]TACATTTGCAAATGT | 286053 |
rs112488451 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161914 | GGCTGATACCTGCAA[A/G]GTCTCACATGCTTCT | 286053 |
rs112489433 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304829 | GGAGGCAGAGGTTAC[A/G]GTGAGCTGAGATCGT | 286053 |
rs112489616 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148260 | GCCATCAAAACTGAC[C/G]CAAGCCTTGCCCATT | 286053 |
rs112493361 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204009 | AATGTCATTGCGGTG[A/G]GACAGATGCTTGTCT | 286053 |
rs112501677 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146949 | ATGTTGCCCTGAGAT[A/T]TGATGTAAGTTTGAT | 286053 |
rs112530279 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266153 | GCTGGAGTGCAATGC[A/G]CGATCTCCGCTCACC | 286053 |
rs112531752 | snp | C/T | 0.444444 | 0.157135 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279029 | TTAGATCAGCTATAA[C/T]CACCACGAGGGGAAG | 286053 |
rs112548632 | snp | A/G | 0.444444 | 0.157135 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194453 | CTATTGCTGAGTAGT[A/G]TCTCATCGCATGGAT | 286053 |
rs112555924 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243434 | GATCTGTTCCAAAAG[A/G]AGAAGATTGTGAGCA | 286053 |
rs112583854 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306426 | GGGCCTTACTGCCCA[A/C]TTTAAATTTCTCTAT | 286053 |
rs112586879 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104164 | CCCAGCTAATTTTGT[A/T]ATTTTAGTAGAGACG | 286053 |
rs112598908 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159957 | AGAGTGAGACTCTGT[C/G]TCAAAAAAAAAAAAA | 286053 |
rs112610311 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210624 | AGCCTAAAAATTGCC[A/T]CATTTTGTTCCTTTT | 286053 |
rs112610417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240415 | GGCTTGAGCCACCAC[A/G]CCTGGCTTACAGCTT | 286053 |
rs112613707 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266256 | GCCACCACGCCCGGC[C/T]AATTTTGTGTTTTTA | 286053 |
rs112616042 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239522 | GTTGAGACATGAGAA[C/T]TGCTTTAACCCGGGA | 286053 |
rs112624913 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112679 | TCACTCGTATGTGGA[A/G]TCTAAAGAAGGTGAA | 286053 |
rs112625578 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304859 | TGCCACCTCATTTCA[G/T]CCTGGGCAACAGAGC | 286053 |
rs112629770 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286228 | TATGTCTTTACAGAG[A/G]TAACACCACCACCAA | 286053 |
rs112632086 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320262 | GGGAGGGAAGGAAGG[A/G]AGGAAGGAAGGAAGG | 286053 |
rs112635202 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302680 | GCAAATGGCCTGTCC[C/T]GAGAAAGGACCCTGA | 286053 |
rs112643346 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195642 | GCTGGGAATATGGCA[G/T]TGAACAAAATAGACA | 286053 |
rs112647749 | snp | C/T | 0.0134861 | 0.0810011 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367322 | GAGTTCAAGACCAGC[C/T]GGGGCAACATGGTGA | 286053 |
rs112660679 | snp | C/T | 0.126909 | 0.217598 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272114 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 286053 |
rs112685145 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196728 | ACCCAGTAATGGGAT[C/G]GCTGGGTCAAATGGT | 286053 |
rs112686376 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216628 | AACAAGAGCGAGGCT[C/G]TGTGTCAAAAAAAAA | 286053 |
rs112687967 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204408 | AGAGGACACTATACT[A/G]TGACTTCACTTCAGT | 286053 |
rs112702969 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122628 | AGCTTAAGTATCATC[C/T]TTTTTCTGCAGACAT | 286053 |
rs112711043 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169650 | TTCAGTCCCCTTGGG[C/G]ACACTGGCTGCACAC | 286053 |
rs112715086 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134792 | GAGTACAGTGGCATG[A/G]TCATAGCTCACTGCA | 286053 |
rs112718407 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122462 | TGGCTATATCCCCTT[A/G]TACTCTATATACTCC | 286053 |
rs112721317 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192575 | GCTACTTGTATAGAA[A/G]TGCATTGTTGGTGAA | 286053 |
rs112723597 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194755 | GTTTTTCAATGTGCA[A/G]TCTATGAGAATTGCA | 286053 |
rs112742490 | snp | C/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356933 | CAAGAAAGAGATCAC[C/G]AGGTCGGTTCTCTGA | 286053 |
rs112762178 | snp | A/G | 0.444444 | 0.157135 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346108 | GTTGCAGTGAGCCAA[A/G]ATCGCACCATTGCAC | 286053 |
rs112762805 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142418 | CATCGTCTCTCTTCT[A/G]TGTCACGATGATGAG | 286053 |
rs112763782 | in-del | -/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316959 | ATTTTTGGTTTTTCG[-/T]TTTTTTTTTTAAGAG | 286053 |
rs112766341 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149556 | TTAGTTGAAATTTTT[A/G]TGTTCCTGTGTTAAC | 286053 |
rs112767521 | snp | C/G | 0.0513262 | 0.151752 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107561 | AGAGAGGAATACAAT[C/G]ATCTATTAGAGTGCA | 286053 |
rs112767956 | in-del | -/A | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257291 | TCCATCTCAAAAAAG[-/A]AAAAAAAAAAAAGAC | 286053 |
rs112768951 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119392 | AGTTTTTAAAACAGC[G/T]TGTATAGTATCTGAA | 286053 |
rs112771289 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181774 | GACTGAGCAGACTTG[A/G]GTGGTGATGCTCAGG | 286053 |
rs112772233 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133798 | AAAAAAAAAGAAAAA[A/G]AAAAAAGAAATTCTG | 286053 |
rs112772376 | snp | A/G | 0.136166 | 0.22258 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198502 | CATTTATTGATTTGC[A/G]TGTGTTGAACCAGCC | 286053 |
rs112796398 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118935 | TCTTGATTTTGTTAT[C/T]GATTACATTTTAAAA | 286053 |
rs112822669 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200968 | ATCGAATCGGGTATT[C/G]AAGCTTGTGCATGCA | 286053 |
rs112824384 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324619 | TGGCTCTGTTGCCCA[A/G]GCTGGAGTGCAGTGG | 286053 |
rs112824993 | snp | G/T | 0.133777 | 0.221342 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215513 | ACATACGTGTGCATG[G/T]GTCTTTATAGCAGCA | 286053 |
rs112825205 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326650 | AGTTTAAAAAAAAGA[G/T]TGGTTAAAAAGATAA | 286053 |
rs112847332 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325660 | CTTAAGCAGCTATTT[C/T]TAAAAATGAAGTTGG | 286053 |
rs112856822 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303033 | TTCTGTTTCGCAAGC[A/G]GAGAGTCCTCACTCT | 286053 |
rs112860325 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091342 | GACATCCATACAGCA[A/G]TGTTCCCGGAAACTT | 286053 |
rs112873511 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257776 | CCTGACTTCATTATC[C/T]GCCCTCTTCGGCCTC | 286053 |
rs112881729 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291630 | TTCAGTGTGATGGAA[A/G]GATTGTTTCCAGTGA | 286053 |
rs112888185 | snp | A/C | 0.242488 | 0.249887 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218661 | AGGTGATCCACCCGC[A/C]TCAGCCTTCCAAAGT | 286053 |
rs112894939 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218237 | AAATACTAACCACCA[C/T]GTCTACTGTAGCTTA | 286053 |
rs112902333 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260925 | CATCATGCCTGGCCA[A/C]ATTTCTTAATTTCAG | 286053 |
rs112929731 | snp | A/G | 0.444444 | 0.157135 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115889 | GCAAGTATGAAATAA[A/G]GGTGTATGTTGTGGA | 286053 |
rs112935960 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337902 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 286053 |
rs112938104 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341560 | TGGTTTTTGTTACTG[C/T]GTTGATTCATCTGTT | 286053 |
rs112943831 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231322 | CAATGACTTGTCTTC[A/G]TAGCTCATCAGTGAG | 286053 |
rs112955874 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354192 | CCACCTCAGCCTCCC[A/C]AAGTGCTGGGATTAC | 286053 |
rs112966549 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132132 | GTACAGGATCTTGCT[C/T]TGTTGCCCAGGCTGG | 286053 |
rs112997185 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202221 | CCTCCATGGGCTGCA[C/T]CAGCTGTCCAACCAG | 286053 |
rs113008390 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350323 | ACTGACATTTTAAAA[G/T]GACAAGAAGGAGTAG | 286053 |
rs113031126 | snp | A/G | 0.444444 | 0.157135 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191935 | AGTCAAGAGGCCACA[A/G]GGATAGCAAATACGT | 286053 |
rs113033294 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179922 | TTAGATCATCCCAGA[C/T]TACATAATAATTTCA | 286053 |
rs113052423 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218595 | TTTTGTATTTTTAGT[A/G]GACGTGGGGTTTCGC | 286053 |
rs113071242 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142025 | GAAGTTAGTAAAAAA[A/C]AACCTAGAGAGCTAA | 286053 |
rs113076857 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146756 | TGTTGTGAGGTGGGG[A/G]GAGTGGGGAAGGATA | 286053 |
rs113078312 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166414 | TGGGATTTCAAGTGC[A/G]TACCACCACACCTGG | 286053 |
rs113081498 | snp | C/G | 0.444444 | 0.157135 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186711 | CTCTCTGGAGCAGTA[C/G]GTACAGAAAGATTTT | 286053 |
rs113086532 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342864 | AGCTACATTTTGGGG[A/G]TTTCACCCACATTGT | 286053 |
rs113088197 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198734 | GTTCCCTCTTTTTCT[A/G]TTGATTGGAATGGTT | 286053 |
rs113095473 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363287 | GCAGGTGGATCACTT[A/G]AGCTCAGGAGTTCAG | 286053 |
rs113118598 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114259 | TTATTAATGTTATTT[A/G]TTGTCTGTGTCTGCC | 286053 |
rs113124881 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215606 | GTTCTAGATCCCTGA[A/G]GAATCGCCTATGTCC | 286053 |
rs113138653 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230809 | GGAGGAAATGGCAAA[A/G]AAAAATCATCTTCAA | 286053 |
rs113141571 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281016 | GAAAACTCTGCCTGC[C/T]TATCCAGAATGGGTC | 286053 |
rs113149983 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299967 | GGGACTACAGGTGCA[C/T]GCCATCATGCTTGGC | 286053 |
rs113155186 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292117 | CTACCTACAAGGAGG[G/T]CTGGACAAAGGTATA | 286053 |
rs113168401 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096660 | TTTTTTTTTTTCATA[C/T]GGAGTCTTTTTGTGA | 286053 |
rs113174405 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214483 | AAATGGGTCACTGGC[A/G]GGGTCAGTACAGGAC | 286053 |
rs113186642 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205101 | ACCTGTAGACTTTCA[C/G]TCTTGCTGATCTCTT | 286053 |
rs113188817 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139549 | GGAGTAGCAGAGTCA[C/T]GTCTTGCATGGTGTC | 286053 |
rs113196669 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146760 | GTGAGGTGGGGAGAG[A/T]GGGGAAGGATAGCCT | 286053 |
rs113207744 | in-del | -/A | 0.0402882 | 0.136092 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234953 | GTCCTGGCTTTTACC[-/A]AAAAAACTTTTCCCT | 286053 |
rs113217937 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103934 | TTTTAATATCCTTGT[A/C]TGTTAATTCTGTCAT | 286053 |
rs113218930 | snp | C/G | 0.01035 | 0.0711892 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181304 | AGAGCCTGTGTAAAG[C/G]TTCTTGAGAAAAGAG | 286053 |
rs113227706 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319915 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCTAGCAC | 286053 |
rs113247784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168930 | ATTACCATGTATTCT[C/T]AACCAGGGTATAGTA | 286053 |
rs113250389 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283771 | CAGTCAACATGTAGA[A/C]CCTAGAGGAACCCAG | 286053 |
rs113263271 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256981 | TGAAGGTGAAACTCT[A/G]GGAGCACCCTGACAT | 286053 |
rs113281284 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125702 | CTTGGTGTCAAGATC[G/T]GTGAAAGCTAACAGG | 286053 |
rs113295955 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096425 | TGCATTTACTATAAG[A/G]ATATTTTTGAGGATT | 286053 |
rs113308628 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101928 | TCAAAATAGTTTACT[A/C]ATAAACTATTTTATT | 286053 |
rs113323154 | snp | A/T | 0.167158 | 0.235875 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257061 | AACCTAAGCGGGCAG[A/T]TCACTTGAGGTCAGG | 286053 |
rs113343081 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297738 | TAGTTGGGAGGCTGA[A/G]GTAGAAGGATCACTT | 286053 |
rs113348745 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203973 | TCCCTAGTCCTTATC[A/G]TGTAATTTACATTTG | 286053 |
rs113357868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358992 | CAGATTTCGGCCAGG[C/T]GCGGTGGCTCACACC | 286053 |
rs113359267 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355060 | GGTCCCATCCCCCAA[A/G]ATATTTCATCATGCT | 286053 |
rs113373442 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272748 | ACACACACATATATA[G/T]ACACACGTATATATA | 286053 |
rs113385152 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139883 | CACTTACTGAAAAGT[A/G]GAGCACAGAGATACA | 286053 |
rs113404905 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125122 | TCATGTCATCTGTGA[A/G]TGGAGATAGTTTTAT | 286053 |
rs113417783 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316663 | TTCCTTCTTTCCTTC[C/T]TTCCTTCTTTCCTTC | 286053 |
rs113419221 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154647 | GGTTTTATACCTGTC[A/G]CAACTCTTTAAAAAC | 286053 |
rs113422504 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098921 | TAGGTGGATGGGAGA[C/G]GATGGAAAAGAGAGA | 286053 |
rs113431074 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264838 | AATACTGAAAAATGG[C/G]CTTATATCTTCTAGT | 286053 |
rs113439053 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220643 | TTAACATCATTATTT[A/T]AAAAAAAAAAAAAGT | 286053 |
rs113440911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224530 | GCATGTGTATCTACA[C/G]TTTTCCCAACATTAT | 286053 |
rs113459606 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276396 | AAACCCCTCTTCCTT[A/T]CTCCAGACTAACTGG | 286053 |
rs113486891 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106201 | GTAGTTCTTCCCTTC[A/C]TAGAGTTTACCATCT | 286053 |
rs113507461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112244 | ACTAAAAGTAAAAGG[C/T]AATGCCTACACCAGG | 286053 |
rs113514482 | snp | G/T | 0.302184 | 0.244493 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201302 | TTTCTCCCCATCTTT[G/T]TGGTTTTATCTACCT | 286053 |
rs113519127 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125366952 | GTCTGTTGAGAGCAG[G/T]GCTGACCCCAGCAGT | 286053 |
rs113526488 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363542 | AGAAAGAAAGAAAGA[A/G]AGAGAGAGAGAGAGA | 286053 |
rs113540652 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194580 | GAGTTTTATGTGAAT[A/G]TGTCTTAATTTCTAT | 286053 |
rs113565816 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270315 | ACTAAAAATACAAAA[C/T]TTAGCGGGGCATGGT | 286053 |
rs113583575 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257154 | TCAGGCGTGGTGGCA[C/G]GTGCCTGTAATCCCA | 286053 |
rs113585868 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111654 | AAAATAGAAAAATTA[A/G]CTGGGTGTGGTGGTG | 286053 |
rs113615853 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163469 | AATCCATGTTCTACC[A/G]GGCTGTGACCTTGGA | 286053 |
rs113626633 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148115 | TTTCCTGTTCCCTTT[A/G]TTGCTTGGGCTGCAC | 286053 |
rs113657412 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271686 | ATCAGGTTTCATAGG[C/T]AGGAGCTCCTGGGGT | 286053 |
rs113680037 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172769 | GTCTTAGCTTTTGCT[A/G]TTGGTTCTGAATCCA | 286053 |
rs113680431 | in-del | -/T | 0.192088 | 0.2432 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167764 | TTTTTTCTTGTAAGA[-/T]TTTTTTTTTTTATTT | 286053 |
rs113699866 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097122 | TCTTTCAATGCAAAT[A/G]TTTGAAGATCATCAT | 286053 |
rs113745523 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218223 | TTTTTTACTGACCAA[A/T]ATACTAACCACCATG | 286053 |
rs113772162 | in-del | -/A | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256282 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs113791699 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104054 | GGAGTGCAATGGTGC[A/G]ATCTCGGCTCACTGC | 286053 |
rs113795367 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144387 | TTTGGGAAAGCCAAT[A/G]GAAAGAATCTTCTGC | 286053 |
rs113806135 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113831 | TGAATGCTTTTGCCC[A/G]TTGGTTGTTCAGGGA | 286053 |
rs113807414 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111346 | TGCTTTGGGGGTAAG[A/C]TTCTAGTTTTGTTCC | 286053 |
rs113813359 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352445 | CACGCCATTGCACTC[C/T]AGCCTGGGCGACAAG | 286053 |
rs113815942 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366123 | AGTCCAGCCAGTGAA[G/T]CTGTGGCCCCAGCAC | 286053 |
rs113827486 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165905 | GCCATATTAATTATA[G/T]AGAAAGCAGTGCCAG | 286053 |
rs113845230 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210737 | ATTTTTGTTTGAGAC[A/G]GGGTCTCACTCTGTT | 286053 |
rs113847407 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193901 | AACTCTCATCATCCC[C/T]ATTAACTGTATGTCG | 286053 |
rs113850437 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125127024 | AATGTACATAACACA[A/G]GCAGCCATGAGTTAA | 286053 |
rs113850586 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238882 | CTGTGGGGTTATTAG[A/T]ACATATATCAAATTC | 286053 |
rs113877424 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291477 | GAGCTGGTCAATGAT[G/T]AATCAAGTGCACAAT | 286053 |
rs113899387 | snp | A/G | 0.5 | 0 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125182222 | TGAAAAATTTGTACA[A/G]TTTAAACAACAGCTG | 286053 |
rs113909087 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097455 | AAAGGGAACTCATCT[C/G]ATCGTTTACTACCTT | 286053 |
rs113915534 | in-del | -/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096541 | TTCTAGTGTTATTTG[-/T]TTTTTTTTTTTTGGA | 286053 |
rs113929083 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151319 | ATATTTGGTTACAAC[C/T]CACTGACCGAGAAGT | 286053 |
rs113931570 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130864 | AAACTGGACTCCCAC[C/T]GTCCACTGTACATTT | 286053 |
rs113976845 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091020 | ATGTTTGAGGGAGCT[C/T]CATGCGCTTGCAATC | 286053 |
rs113985617 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114615 | CACAACTCGGGGATG[C/T]GGGGAGCATGTGTGC | 286053 |
rs113990845 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155387 | CTTCAGAGTGCCTTA[A/G]TCAATCCAAAGACTT | 286053 |
rs114008470 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252862 | AAGAGCGCAAGCTCC[A/G]GAAAGAGCCAAGGTT | 286053 |
rs114009835 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273202 | CAGCCTATTAAAGAC[A/G]CCAGTGAGACATTTT | 286053 |
rs114020643 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338853 | CAAGGACCGAATTAG[A/G]CTATCATGGTGCTTC | 286053 |
rs114023460 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147755 | CCCAGCAACTTTTTA[A/G]TCAGTAACTCTGTGT | 286053 |
rs114025440 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140547 | GGGTGCCTGTAATCC[C/T]AGCTACTCAGGAGGC | 286053 |
rs114035769 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244909 | CACTGTACTTTGTAT[A/G]CTACAGAAAGTAATT | 286053 |
rs114038581 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112453 | CATATTCACTGCAAC[A/G]TTATTCACAATAGCC | 286053 |
rs114042998 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270486 | AAAAACAAAACAAGA[C/T]GAAAAACAGAATCTG | 286053 |
rs114066130 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304119 | CGTGGCTGTGAATTT[C/T]AGTTTTTGACTGATT | 286053 |
rs114074401 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120039 | TTAGAAATGTTTTAT[C/T]TAAACAAATATGTCT | 286053 |
rs114076341 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146033 | AATTTTCTTTTTGTT[A/G]TCAGATTTCTTAAGG | 286053 |
rs114078726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201957 | GCGAAGCTTCAGCCT[C/T]GCAGGTTCTCAGGCT | 286053 |
rs114118846 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350493 | AGGTTGCGTATTAAT[A/C]CATTTTCATGCTGTT | 286053 |
rs114157524 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303640 | CACTGTAAGTACTGT[G/T]AACTATATATTCCAA | 286053 |
rs114160822 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114089 | TCTGAACATAAATAT[G/T]TTGCCCGGTATGTCT | 286053 |
rs114161746 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284701 | TGAATCTGAATCTAA[A/T]GAGAGGGCTTTATTG | 286053 |
rs114172363 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206586 | CAAATAAAGTAGACT[C/T]AGGAGAACAAGGAGT | 286053 |
rs114178144 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263451 | TACCATGTTCATGCT[C/G]TAGAAAGAAGTAAGA | 286053 |
rs114201447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189167 | ACAGAGACAAAGGAC[C/T]TCTCAGCAAGGCAAT | 286053 |
rs114208587 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356290 | ATGTTTATGGTAACA[C/T]GTAGTGGGATTATTA | 286053 |
rs114238683 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122784 | TTCAACCTTATACTT[C/T]AGCATAAGGTATTCT | 286053 |
rs114279124 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100572 | ATTTTTTTTATTTTT[A/G]TTTTTTTGAGACCGC | 286053 |
rs114290256 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352959 | GGTCTCTTACTCACT[C/T]GTGACATTCTTCCCC | 286053 |
rs114324621 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329693 | TAAGTATGGCCTCTG[A/G]GATCAGACTTATTAG | 286053 |
rs114326621 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243517 | AAAAAAAAAAACCTC[A/T]AAATTTCTAATGTGT | 286053 |
rs114353223 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231412 | AAAGGGATTAAAGCA[C/T]CTGAAGACCTTTGTT | 286053 |
rs114359660 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358503 | AATATATATAATATA[C/T]ACACACACACATATA | 286053 |
rs114377590 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255374 | AGCAATGTAGATTAC[A/G]ATGACAGTGATATTT | 286053 |
rs114386515 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149154 | TTGGGGAATGTAAAT[A/T]CAAATTTTTCTTATG | 286053 |
rs114410362 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119410 | TATAGTATCTGAATA[C/T]CATCTGGGTTTTTCT | 286053 |
rs114450244 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281167 | ATGAGAAAGTTATAG[C/T]TAGCTCTTTTCCCAA | 286053 |
rs114453877 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256654 | AGGACTGTTGGGTGC[A/G]GTGGCTCACGCCTGT | 286053 |
rs114470647 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319545 | TGTGTGGGCAGTGGG[A/G]GTGTATGTCTTTACA | 286053 |
rs114471817 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289271 | GGCAGTTATCCAAAG[C/T]ATCACTCATGCAGCT | 286053 |
rs114477262 | snp | A/T | 0.0596104 | 0.162024 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117191 | GCTGCTGCTTAATTT[A/T]AAAAATCACCAATAT | 286053 |
rs114490947 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252250 | CACACCCCTACCGGC[C/T]GGGCACAGTGGCTCA | 286053 |
rs114536316 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227587 | CAAATGTATTGCAAT[C/T]CATATTAAAAATCAG | 286053 |
rs114574104 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128454 | GAAATTGAGGAAAAG[A/G]AAGAAGTCAATGGTG | 286053 |
rs114581170 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184154 | AATTCCTGAGTTTTA[A/G]GTAATTTTATAATAC | 286053 |
rs114598485 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332922 | TGTGCTTGGAAATCA[C/T]CCAGTTTGGGACCTC | 286053 |
rs114620416 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111828 | TGGTTTGAAAATTAC[C/T]TGATAATTGGATATG | 286053 |
rs114657751 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275002 | CAATCTGAAGATGAT[A/G]ATAATAATAATAATA | 286053 |
rs114658835 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242320 | GAAGAAAAGCAATAT[A/G]GCAGCAACAGACAGC | 286053 |
rs114694737 | snp | C/T | 0.030278 | 0.119257 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188043 | TTTGTATCAGACATA[C/T]AGAGACATAGGAATT | 286053 |
rs114711131 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101397 | TGTATGCTATACCAT[A/G]CCATGGTTATTCCTT | 286053 |
rs114718145 | snp | C/T | 0.00662764 | 0.057183 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357667 | AACAGCTACTGGAAG[C/T]TGATCATTATCATTC | 286053 |
rs114724308 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096270 | CAAGGAAGGCTGGAA[A/C]ATGTGGAGCATATAT | 286053 |
rs114765882 | snp | A/C/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114521 | ATGTATACATACATA[A/C/T]GTACATATGTATATA | 286053 |
rs114774990 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269525 | CTCACTGCTTGATCA[A/G]TTTATTTCCTGTGCT | 286053 |
rs114796959 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302066 | CAGGATCATGTGATT[C/G]TCATGCCTCAGCCTC | 286053 |
rs114798747 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282962 | AGGTAGTCTAGCATA[A/C]TTGTTGAAAGAGCAA | 286053 |
rs114818697 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262777 | CCTCCTCTCTGCAGT[A/G]GTATTGCTCACTCTG | 286053 |
rs114826149 | snp | G/T | 0.030665 | 0.119967 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355329 | AAAGAAGGAAGGGAA[G/T]GGAGAAAAGAGTAGA | 286053 |
rs114838201 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287788 | CATTGGCAGCCCGAT[C/T]TCTTCCACCATTCCA | 286053 |
rs114890369 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130754 | TTAAGGGGAACATGT[A/G]TTCACACCATTATCT | 286053 |
rs114898697 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184821 | TGTGTAGCCAGGTCA[A/G]AGGTACACTATGATA | 286053 |
rs114904289 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261787 | GCTTAGAAGCTTTTG[A/C]AAAACATTTTTAAAA | 286053 |
rs114983233 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093836 | CGTCTCACTCTTATC[A/G]TCCAGGCTAGAATGC | 286053 |
rs114989247 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126268 | GGGTGCCTACTAAGG[A/G]GGCCGAGGCAGGAGA | 286053 |
rs114991903 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179163 | CTGAGATTCTAAGTC[C/G]TGTATCTGGGTAGAC | 286053 |
rs114999446 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343645 | CCCTGTCTAAAAATT[A/T]AAAAAAAAAATTAAA | 286053 |
rs115024938 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351215 | AAAATTGGGAACTTA[C/T]ATCTTGGGGTCCAAT | 286053 |
rs115028807 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172164 | AAAGGTTAAAGACCT[A/G]GATAATCTGGTTCCA | 286053 |
rs115029586 | snp | G/T | 0.0494327 | 0.149241 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201949 | GCCTTCCTGCGAAGC[G/T]TCAGCCTCGCAGGTT | 286053 |
rs115031457 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305731 | TAGGAGTTTAGAAAC[A/G]CTCATATACCTATAT | 286053 |
rs115032866 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227280 | TAGCTCGGTGTCTCC[A/C]TCAGTGGTAGCTGAT | 286053 |
rs115092875 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173368 | TGCTTCTGTCCCTTG[A/G]TTACTGGGCCCTGTA | 286053 |
rs115180160 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353053 | AAGTTCCCCACTCAG[C/T]CTTCCCTAGTGGTAG | 286053 |
rs115185771 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338765 | GTAGTTGGGTTATAA[A/T]TGAAATTTATTCTAG | 286053 |
rs115206076 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148482 | AGGGAGATTGCTAAC[A/G]TTATATCTATTTCCA | 286053 |
rs115207903 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123295 | ATGTTTTAGTTTCCT[A/C]CTTTCCAAAAGCCCT | 286053 |
rs115209505 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213240 | AAAGCAAAATGAATC[A/G]TGCCATTGGAAAATG | 286053 |
rs115211560 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174687 | TTTTCACAATTTTTC[C/T]GAAAGGCTCGAAGGA | 286053 |
rs115225408 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339690 | TTTGCCTTTGCTCAT[C/T]CTACTCCTTCTCCTT | 286053 |
rs115235431 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345683 | GAATTGAGTCTTGGA[G/T]GGTGGTCAGAGATTG | 286053 |
rs115244470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306708 | GGACTTTATCTTGAT[A/G]TCCAGTCTTCATTTT | 286053 |
rs115256389 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366192 | ATAAGGTGACCTGAA[C/T]TTGCAGCAAGCATTT | 286053 |
rs115282650 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264807 | CATTAACTCTTCCAA[C/T]TCTTTATAAAATAAT | 286053 |
rs115313055 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308567 | GAGACTATAGGTTGT[A/T]TCTGGGGAAGGGAGC | 286053 |
rs115355578 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189083 | TATTCAACTTAGAAA[C/T]GTTTTACTTTGTCAT | 286053 |
rs115357046 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361075 | TGATTTCCTTTTTTT[A/T]TTTTTCGTTTCTTTT | 286053 |
rs115376097 | snp | C/T | 0.0014332 | 0.0267309 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125357768 | CACCTATGAAGAGGA[C/T]GCCATTGTTCGCATG | 286053 |
rs115380723 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312779 | AGCCTTTTGTCCAGT[A/G]GCAGGATGGGGTGGG | 286053 |
rs115407559 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233083 | GTAAGGAATCTGAAG[C/T]GTGGCAGATCACTTT | 286053 |
rs115409532 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224035 | GTAGAGAGGAGGTCT[A/G]GCTGTTTTCAGGCTG | 286053 |
rs115410039 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256451 | AGAGTACAGCTTTGA[C/T]GTGCTGGATATGTAA | 286053 |
rs115413078 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278170 | GAAGCATGGGTATTT[C/T]ACATTATTATTTTGT | 286053 |
rs115457475 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349302 | CCCAAATTTTCCAAG[C/T]ACCAGCTCAGCCTTT | 286053 |
rs115461953 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302373 | CTGGTGTGGGAGTTG[G/T]CCTGGCACACATTCC | 286053 |
rs115482590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125683 | TGAGAAGAGCTGTGA[A/G]CAGCTTGGTGTCAAG | 286053 |
rs115500451 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323984 | CCAAAAATGGAAAAA[A/G]GATTTTGAAAAGATA | 286053 |
rs115501845 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286990 | CTGTAACGTGCCTCC[A/T]CTGTAGGGTGGTTTT | 286053 |
rs115520370 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319664 | TAGACACTGCAGAAG[A/G]GAAGACTAGTGAACT | 286053 |
rs115527786 | snp | C/T | 0.0256215 | 0.110247 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093577 | AAATAAATAACATAA[C/T]TGGTGTGTCCTGGCA | 286053 |
rs115530289 | snp | A/G | 0.130694 | 0.219696 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257037 | GCCTGTAATCGCAGC[A/G]CTTTGGGAAACCTAA | 286053 |
rs115564625 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155366 | TTCTGATTGTCTTGA[C/T]GTCAGCTTCAGAGTG | 286053 |
rs115566093 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185263 | GTGGCTCAGCAGCTG[A/G]TTCTCAAAGTTTTTG | 286053 |
rs115566480 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211366 | TTAATGGTAGCATAT[G/T]GGATACTCTGTTCTA | 286053 |
rs115580420 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328218 | TCAGAATCATGTCCA[C/T]AAGAAACAATATTCT | 286053 |
rs115581197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117809 | TGATGTCTTCAGAGT[C/T]TGGGACTTTAATGCC | 286053 |
rs115582454 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303827 | TGCTCTCATGGTGTA[A/G]AATTTCATTGCATCA | 286053 |
rs115594496 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295934 | GATCTTAAACTACTG[C/T]ATAATCCTGAACCAT | 286053 |
rs115611189 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096297 | ATATAGGCATGTAAC[C/T]GGGTTGAAGAGGAAA | 286053 |
rs115654578 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138474 | GAAGTGATCCTCCTG[C/T]CTTGGCTTCTCAAAG | 286053 |
rs115662426 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331845 | CAGGGGTAAAATTTC[A/G]GAAGGAGCAGTGGAA | 286053 |
rs115688911 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105051 | GATTCCTCCTCCCTT[C/G]CGCAGGGAGGAGGCC | 286053 |
rs115692988 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188244 | GTGGCTTTTCCGTCT[C/T]CTTCAGCATCTACTC | 286053 |
rs115704328 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284408 | GCGGAGTCACATGGG[A/G]GTTTGAGACTGACCA | 286053 |
rs115757532 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355391 | AGGACTACACCATCA[A/G]CATGTTTAGAAAGCT | 286053 |
rs115760589 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331404 | ACCTGTAAAATTGTT[A/G]TCAGTACTCAGGGCC | 286053 |
rs115765270 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112448 | CTTCTCATATTCACT[A/G]CAACATTATTCACAA | 286053 |
rs115767671 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131710 | TCTTAGAGGCACCTG[G/T]GATGTATATTTTAAA | 286053 |
rs115808833 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148495 | ACATTATATCTATTT[C/T]CACTGATTTAAGCCC | 286053 |
rs115814644 | snp | C/G/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237599 | TCACTATCAGGCTGA[C/G/T]AGAGTAATTCAGTTA | 286053 |
rs115816345 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275309 | TCCCGTCTTCTAGCC[C/T]TCTCATGTCATTTGT | 286053 |
rs115910649 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124659 | TAATTTTTGTATTTT[C/G]TAGAGACAAGGTCTT | 286053 |
rs115911086 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181184 | ATGAGAAGGTGGAAA[A/G]AGTGGCTCCTTTTTT | 286053 |
rs115923709 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231574 | TTTGCACACTATAGA[G/T]TGCAACCCACAGTAT | 286053 |
rs115932774 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317145 | CCCTCAAGATGAGTC[C/T]ATCCTGGGAAAAAAA | 286053 |
rs115959683 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271981 | CTATTTAGCCTTACA[C/T]TGACAACTGAATATT | 286053 |
rs116001620 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341884 | TGTGCAATGCACTGA[A/G]GATCTAGAAATGGAA | 286053 |
rs116018655 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102705 | TTCCATGAGAAACTG[C/T]GCTAGAAATGTATGG | 286053 |
rs116020555 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157417 | GAACATTGCTCAGGT[G/T]TGGAAATTAACCAGA | 286053 |
rs116055385 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362423 | ATGTCGTTAGCACCC[C/T]ATGTCATGCCAACAT | 286053 |
rs116057166 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337144 | TGTAGTCTTGAGGTA[C/T]GGAAAGAATGGGCAA | 286053 |
rs116099404 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226874 | CCTCTTTTCTCTCCC[C/T]GTTTCATGGCACTGC | 286053 |
rs116101289 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267555 | CTTTGGAAGGCTGAG[A/G]CGGGAGGATCACTTC | 286053 |
rs116102956 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217220 | TATTACATATTATGC[C/T]TGTGCTAGGCTTTCT | 286053 |
rs116136958 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264548 | AGTACCTGGGACCAT[C/T]TGCGCGCACCACCAC | 286053 |
rs116139946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219092 | CCCTGAACACCAGTC[C/T]ACTAAATCTACTTTA | 286053 |
rs116151359 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279035 | CAGCTATAACCACCA[C/T]GAGGGGAAGTTTTTT | 286053 |
rs116170099 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233898 | AGAAAAATCTCTGAC[C/T]GGGCATGGTGGCTCA | 286053 |
rs116224088 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225477 | GTTCCTGAGAGAGCT[G/T]CAAAAAGAGGTTGAA | 286053 |
rs116262046 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136964 | AAATATAAGGAGAAA[C/T]GCAAATTGAATGGGA | 286053 |
rs116283236 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342053 | AGACTCCTGGGGACC[A/C]CTGAGTGAGAAGTTT | 286053 |
rs116286198 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353902 | AACTAAAAAATAAAA[A/T]ATATATATATATATA | 286053 |
rs116290799 | snp | A/G/T | 0.0429648 | 0.14013 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347954 | GTTTAGAAAATGTAC[A/G/T]CTGAAAGATCTTCCT | 286053 |
rs116330125 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094082 | GTGCTGGGATTATAG[A/G]CATGAGCCACCACAC | 286053 |
rs116330297 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144054 | AGGGAAAAGAGGGGG[A/G]GAAAGTCCTTATTTT | 286053 |
rs116336363 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245400 | TAATTTGAAATTTAA[A/G]AAAGAAACTTATCTA | 286053 |
rs116369510 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212200 | TCAGGCTCTTTGCTA[C/T]CGACTTTTACCTTGT | 286053 |
rs116378582 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355096 | AAATATTTCAAAGTC[C/T]GAAATCCGAAACACT | 286053 |
rs116380486 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307902 | CACATAGTTGTATAC[A/G]CATATGTCAGTTTGT | 286053 |
rs116422054 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147863 | AACAAAAAAGAATTA[C/T]GAAAATCCTCTTAAA | 286053 |
rs116423563 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152627 | TCTATCTTTAACTTT[C/T]ATACTGTGCAAATGC | 286053 |
rs116440547 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167697 | AATTATGCTAAAGGG[A/G]TGGGAATAGTTTAGG | 286053 |
rs116474984 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188333 | TCCTTGAACTCCAGC[A/T]TGAGGCCTAGGTACA | 286053 |
rs116479103 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230472 | TTATTGATGTTCAAA[A/G]CGTGAACATCCCTTG | 286053 |
rs116496039 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204382 | AGAAGGTACTTCCTT[G/T]CTCTTTCCCGAGAGG | 286053 |
rs116496493 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248847 | GAGGATCATAGTAGC[C/T]TGCCCTAGGGCACTC | 286053 |
rs116516623 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157098 | AATATACCCCACTCT[A/G]TTAGGCATTGTGAAT | 286053 |
rs116535675 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226487 | TTCTTGCACTGTACC[C/G]CTCATATCTGCAGCC | 286053 |
rs116543246 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300450 | TTACAGACATGAGCC[A/T]TCACACCTGGCCCTG | 286053 |
rs116567331 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136483 | CTTGCATATAGTTTG[A/G]TTCTGTTTGGTTGCA | 286053 |
rs116576203 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296745 | TCCTTTTCCTCCTTC[A/G]TATTGTTGCTTACAA | 286053 |
rs116591028 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257475 | AAGATAAGGATTGAG[A/G]AAGGGTCATTGGTAA | 286053 |
rs116607473 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269156 | CAAGTGACACGATCT[C/T]GACTCACTTCAACCT | 286053 |
rs116620102 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119033 | CCCAGTTGTATTTGG[A/G]GCAGTTTTAGAATGT | 286053 |
rs116641755 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244863 | AAAGATATAGAGGAG[C/T]GACTGCTCAAAGCTT | 286053 |
rs116654617 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125363939 | TGTAGGGCACTTTTT[G/T]TTTGTTTGTTTTGTT | 286053 |
rs116657398 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279171 | ATTACAAAGCTATGT[C/T]GGATAAATATTTTGA | 286053 |
rs116662167 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193158 | GAGTTAACAGGGTAT[A/G]AAGTTGAGTATTCAG | 286053 |
rs116662396 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147741 | CAACCACCCCAACCC[C/T]CAGCAACTTTTTAGT | 286053 |
rs116663679 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265785 | AAAATGCCTAGTTTT[A/C]TTTGTCTCTGAACAT | 286053 |
rs116680659 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346756 | CAAATCTTAACTGAC[A/G]ATTTTTGTCCTACCA | 286053 |
rs116687010 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359257 | GGTCACAGAGTGATA[C/T]TCTGTCTCCAAAAAA | 286053 |
rs116733656 | snp | A/T | 0.189576 | 0.242588 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216211 | ATTTTGTTGATCCAC[A/T]TATCTGTCAATGGAC | 286053 |
rs116767727 | snp | C/T | 0.030665 | 0.119967 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303178 | AGGCAGCTTTCAGAG[C/T]AGCTGCCTCCCTCTG | 286053 |
rs116790770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276586 | ATGGTTATTATATCT[C/G]ATTGTATATACAGTC | 286053 |
rs116794286 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363369 | AAATTAGCCAGGCGT[C/G]ATATTGTGCACCTGT | 286053 |
rs116824114 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144473 | ACAAATACGGTATGA[A/G]CAGACCTTAGACAAT | 286053 |
rs116827100 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201612 | TGTCTGTCAGTCCCT[A/G]CTGGGAGTTGTCTTC | 286053 |
rs116845445 | snp | A/C | 0.120326 | 0.21374 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349079 | GAGCTCTTAATTCCA[A/C]ACCAAAAGAACTGAG | 286053 |
rs116893885 | snp | C/T | 0.0798611 | 0.183174 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178834 | GAGATCGTGCCACTA[C/T]AGCCTGGGCAACAGA | 286053 |
rs116902257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143849 | CAGACACACATCCAC[A/G]TGTCCCAGTTGTAAA | 286053 |
rs116909124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285040 | GAAAAGGATTCTAAA[C/T]ATAGTCTGAATTAGA | 286053 |
rs116924795 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256644 | AAAAAAGAAGAGGAC[A/T]GTTGGGTGCGGTGGC | 286053 |
rs116941673 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212053 | GGGCAAAGTCCATCT[G/T]TCTCTATAATTTTGA | 286053 |
rs116943625 | snp | A/C | 0.119978 | 0.213528 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361523 | GTTTCAACACTTACC[A/C]ACAAGCCATTCAACC | 286053 |
rs116988112 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149111 | TGAGCCTTTTCTCAC[A/G]CACCATTTTGTTAAA | 286053 |
rs116988888 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268967 | AGATCATGACTTTTT[A/C]AAAAATATATTGTTT | 286053 |
rs117014610 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208931 | AAGATTGCTGTCAAT[A/G]TTTTTTTCCTCTCCA | 286053 |
rs117021190 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251297 | CAATAATGACATAAT[A/G]CAGAAAATGCCCACA | 286053 |
rs117071226 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216367 | CTGTGGGTCCGGGCG[C/T]GATGGCTCATGCCTG | 286053 |
rs117102317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299570 | GTTACCTCCCACCAG[A/G]TCCCTCCCTCAACAT | 286053 |
rs117111236 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289693 | TAGCAGATGTTTGTG[A/G]GTGTGCTGTTACTGA | 286053 |
rs117134698 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162010 | GTCCTCTCTACCCAT[C/G]AGGTCACTTTCTGTC | 286053 |
rs117138138 | snp | A/G | 0.220246 | 0.248223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263623 | GGCATGGTAGCACGC[A/G]CCTATAATCCCAGCT | 286053 |
rs117148127 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149932 | TGTAGGGATTATTTG[A/G]CACTTAGATTAAGAG | 286053 |
rs117239170 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342649 | CTCCCTCCCTCTTTC[C/T]CTCCCTCTCTCTTAC | 286053 |
rs117240888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313828 | CTTTGCAGAACAAAA[G/T]GAAAAATCAAAGGGA | 286053 |
rs117245903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105715 | ACGTAAATGAATGGG[C/T]ATGGCTGTGGTCTTA | 286053 |
rs117298205 | snp | A/T | 0.04875 | 0.148319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346330 | AAGAGGAGGAGACAG[A/T]CTCAAGATAAAGATG | 286053 |
rs117320681 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302534 | GTTAATATGGGGTGA[A/G]AATTGAGAGAAGAAT | 286053 |
rs117322553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162194 | ATGTTTTGAAAAGCT[A/G]CAGCAATACTTCTCA | 286053 |
rs117364311 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114540 | CATATGTATATACAG[C/T]AGTGGGTGATTTTGC | 286053 |
rs117387645 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365000 | GAGAAGAAATAGGTG[A/G]TTTCATCCAGCCCAC | 286053 |
rs117398403 | snp | C/T | 0.11963 | 0.213316 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343271 | ACAGGTACTTCCTCC[C/T]TCACTGCACTTTATC | 286053 |
rs117402444 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287804 | TCTTCCACCATTCCA[A/G]TGAATCCTCTCTGCA | 286053 |
rs117428419 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296005 | TTAAAGTATGAGTAG[A/G]AATTACAGCTTACAG | 286053 |
rs117472523 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341602 | TCCTCTAATGAGGGC[A/G]AAACACTTGATCCCA | 286053 |
rs117473134 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204778 | CCTAAAAATCCCTAC[C/T]AGTCCCCTCTCCATT | 286053 |
rs117475948 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128475 | GTCAATGGTGATACT[C/G]AAATTTCTGACATAC | 286053 |
rs117487674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300958 | AGTGGTCATCTCAGT[C/T]CCAAATAGTGTCCTG | 286053 |
rs117507314 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290998 | ATTCAGTAAATATTG[A/G]ATGAACAGAAACTAA | 286053 |
rs117520433 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246525 | GAGCTTCAAATGGCT[A/G]ACAACTATAAATGAC | 286053 |
rs117538404 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141046 | GATTCCCATAGCCTG[A/G]GTTTCCATAGTGTTT | 286053 |
rs117538685 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155664 | TATTAAATAAACCCA[A/G]TGGTAGTACTGTGTG | 286053 |
rs117567029 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183689 | CACATGGACCTGTGA[C/T]TACCAGCCTGAGGCC | 286053 |
rs117588701 | snp | A/G | 0.131381 | 0.220067 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279598 | TAAGTGGCAAAATGC[A/G]AAAGATAGAAATGCA | 286053 |
rs117639451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289973 | AAAAGCTGGTGTACA[C/T]ATGTGATAGTGTTTT | 286053 |
rs117639622 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110413 | TTAATTGGGTATTTG[C/T]TGAGCTATGCTAAAG | 286053 |
rs117640147 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116052 | CCCAACTCCAGCCCC[A/G]TGACCTCGATTTATC | 286053 |
rs117645378 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115550 | GAAGTCAGGAGTTCA[A/G]GACCACCCTAGCCAA | 286053 |
rs117687969 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161178 | GGATTTCTTTCCATT[G/T]TTTCTCTCTCACAGC | 286053 |
rs117717436 | snp | C/T | 0.130434 | 0.219819 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267302 | CTGAGCCACCGCGCC[C/T]AGCCAAGGGTACCTT | 286053 |
rs117723884 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340924 | CCCTGCATAATTTCT[C/G]TGCCTCCTTGATGTT | 286053 |
rs117727295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301318 | AGTAGTCATCTAACC[C/T]GAGGTTTCCCTGGCC | 286053 |
rs117766003 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119634 | AGTTTAATGCTAAGC[A/C]AAGATGACAGCTTAT | 286053 |
rs117768435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219282 | TTCTACTTAATTTAT[C/T]TGGCTGGATTCCTGT | 286053 |
rs117777830 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355212 | ACAGTCATCAGTTCT[A/G]TGGAACCGAAAGGTA | 286053 |
rs117781948 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338781 | TGAAATTTATTCTAG[A/G]AGTAATAAATATGGT | 286053 |
rs117802090 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150819 | GACAGAGCTGCTTAA[C/T]GGATGAGGGAACTGA | 286053 |
rs117807542 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167802 | CATGTTTTCTACATT[A/G]GAAATGCAAGCATTG | 286053 |
rs117837183 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272473 | AGGTGACCAAATGAC[C/T]AACCCGGCACATGGG | 286053 |
rs117838314 | snp | C/G | 0.131723 | 0.220251 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296029 | CTTACAGCTTAGATT[C/G]TGATCTTTGCACTGA | 286053 |
rs117842178 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342551 | AGGACTTTGTTCTAC[A/G]ATGCTGACTCAGTGA | 286053 |
rs117854049 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321390 | AGGGAGAAATGGAAT[C/T]ATACTGTTTTAAGGC | 286053 |
rs117869713 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364236 | GGTGTGAGCCACCGT[A/G]CCTGGCCATATTTTA | 286053 |
rs117885323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340773 | TGTTCAGATGAATAG[A/C]CCTCAGTCTGGGTGA | 286053 |
rs117886682 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268271 | TTTTTGAGAAGGTCA[A/G]CATTTGGTTAGTGAA | 286053 |
rs117887824 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156555 | GCAAGTAGGTGCTAG[G/T]TTGGTCCATTTGTAT | 286053 |
rs117888045 | snp | C/T | 0.139225 | 0.224118 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245898 | AGGTGTGGTGAGGCA[C/T]CTGTAATCCCAGCTA | 286053 |
rs117890183 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143732 | GGAAACAGCTTGGCC[A/G]TGGGCAAAACTATAC | 286053 |
rs117896352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329830 | ATTGTGAATTAATTC[A/T]CACAGTGTTCACTCA | 286053 |
rs117988468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313346 | AGGTAGGAAGAGGCA[A/G]CCCTGATAAAAGTCA | 286053 |
rs117995962 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206149 | TGTATTCTGATCACC[A/G]TGACCAGGTAAGGAA | 286053 |
rs117997370 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219167 | ATTTGCTATTTGGGG[C/T]CTGGGGAGGCAGATA | 286053 |
rs117999801 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231154 | TAAACCTTACAGTCC[C/T]AGAAAGAAGCATTAA | 286053 |
rs118029319 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277009 | TGGTGTTCTGATGGC[A/G]CATGAGATCTTTCTT | 286053 |
rs118097749 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167638 | GACTCAGTCTCAAAA[A/G]AAAAATTGCAAAGTC | 286053 |
rs118118114 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094578 | AGCTACTGTTTGGTA[G/T]ATACTTTCCATTTAT | 286053 |
rs118144463 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280009 | TTTTCCTTTTGGACT[A/G]TAAATTCCTCGAGGG | 286053 |
rs118152380 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174802 | TGTCGTAATGCTCAA[C/G]AAGGAAGTATTCTCT | 286053 |
rs118162018 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107762 | AAATAAGCTAGGCCT[C/G]GTGGCTGACACCCAT | 286053 |
rs118169109 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207072 | CTAAATAAAATTATT[A/C]ATACTTTTCATATTC | 286053 |
rs137860970 | in-del | -/AA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312092 | AAAAAAAAAAAAAAA[-/AA]AGAAAGAAAAGAAAA | 286053 |
rs137882065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210198 | TTCAAAGGATTGTTG[A/T]GGAGATTCAATGAAT | 286053 |
rs137887576 | snp | A/G | 0.135143 | 0.222054 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326722 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 286053 |
rs137895376 | in-del | -/CTTCCTTCTTTCCTTC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316687 | TTCCTTCCTTCTTAT[-/CTTCCTTCTTTCCTTC]CTTCCTTCTTTCCTT | 286053 |
rs137898853 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241063 | AATTTTGGAATATTG[A/G]CACTATTCTTACGGG | 286053 |
rs137901077 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204241 | CCTTTTTGCGAAGGT[C/T]ACCTTGGCAGACCTG | 286053 |
rs137912291 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279159 | CATTCCACTCTTATT[A/G]CAAAGCTATGTCGGA | 286053 |
rs137921232 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324066 | TAGATGACAAGCACA[G/T]GTAAAGATGCTCAGC | 286053 |
rs137933655 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176411 | TTTCTTTTTAAACTC[G/T]TCTAGCCGCCCTTAA | 286053 |
rs137953740 | snp | C/T | 1.65466e-05 | 0.00287628 | missense | NSMCE2 | GRCh38.p7 | 8:125357802 | GAGTCCAGGCAAAAG[C/T]GGAAGAAAAAGGCCT | 286053 |
rs137956390 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359625 | GGCATGAGCCATCGC[A/G]CCCAGCCATGGCATG | 286053 |
rs137996655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291362 | ATAAAATTTTAATAA[A/G]TTTAATTAATGTTTG | 286053 |
rs138002102 | in-del | -/TGTG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183642 | CTCAGTGGTGTGTGT[-/TGTG]GTGTGTGTGTGTGTG | 286053 |
rs138013970 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310500 | AGCTTTTTGTTTGGT[G/T]TATTCAATATGGTTT | 286053 |
rs138019153 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137408 | GCTGACCCTATTCGT[A/G]TCTTTTTCTTGGTAT | 286053 |
rs138028152 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118271 | GGATCACTTGAACCC[A/G]GGAGGCTAAGGTGGG | 286053 |
rs138033540 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236260 | CTGGTGGTAGCTGTA[C/T]GGGATAATTATTTTC | 286053 |
rs138036446 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351939 | AATCATTTGAACCCA[G/T]GAGGCAGAGGTTGCA | 286053 |
rs138052411 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250115 | CTGCCTCAGCCTCCC[A/T]AGTAGCTGGTACTAC | 286053 |
rs138072255 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170770 | CTCACTGTTTCTCCT[A/G]CTGTCACCCTAATCC | 286053 |
rs138108601 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202734 | ACATATACTTAAATT[G/T]TATAAGGATAAACAT | 286053 |
rs138126365 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273770 | TGGCCCTGTTCCTCA[C/T]TCATATTGCAGATTG | 286053 |
rs138127096 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266270 | CTAATTTTGTGTTTT[-/T]AGTAGAGATGGGGTT | 286053 |
rs138141220 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303275 | ATGTTGTTCTCAACT[C/G]AATGGACACACCCTA | 286053 |
rs138141803 | snp | G/T | 0.0832709 | 0.186283 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199751 | ACCTTCTGTCTTGTT[G/T]ATCAGTCTAATATTG | 286053 |
rs138178797 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271043 | GAGGCAGGTGGATCA[C/T]GAGGTCAGGAGTTCA | 286053 |
rs138205199 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148469 | CATTTAATCCCAGAG[A/G]GAGATTGCTAACATT | 286053 |
rs138214266 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231348 | GTGAGTTCACAGTCT[A/G]TTGTTCCTTTTTATT | 286053 |
rs138219984 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346889 | TGTCTGCAACAACAG[C/T]AGATAAATTATAAGC | 286053 |
rs138228056 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191896 | TAAGAATCTTGGAGG[C/T]GACATATTTACCCAG | 286053 |
rs138242898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144466 | ATACTGAACAAATAC[A/G]GTATGAACAGACCTT | 286053 |
rs138252985 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226631 | TCCTGGAGGACGAAA[C/T]GCCACTTGTCTGAGA | 286053 |
rs138291649 | snp | C/T | 0.140581 | 0.224783 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198450 | ATTGAGATAAGCATG[C/T]GGTTTTTGTCATTGG | 286053 |
rs138300767 | in-del | -/AAGAA | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179369 | AACAAAAATTCTCCT[-/AAGAA]AAGAGGGGCATCTTT | 286053 |
rs138313353 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138340 | GTGATCCTCCCACCT[C/T]GGTCTCCTGAGTAGC | 286053 |
rs138333851 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186393 | AGTAACGGCAGTTTT[A/T]ATTTTTTTAATTTTA | 286053 |
rs138355373 | snp | A/G/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200199 | ATATTGTTATGTTTG[A/G/T]ATTTGATCCTGTCAT | 286053 |
rs138358378 | in-del | -/TTAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192525 | ATATGTATATGGTAG[-/TTAA]CAAATAGGGAAAAAA | 286053 |
rs138360631 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181191 | GTGGAAAGAGTGGCT[-/C]CCTTTTTTCCCCCAA | 286053 |
rs138380158 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250146 | AGTCATGCACCACCA[C/T]GCCTGGCTAATTTTT | 286053 |
rs138382259 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317477 | TCTGGGATTACAGGC[A/G]TGCACCACCACACCT | 286053 |
rs138401167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158804 | AGTGGTGCTGAATGG[A/G]CTAACTGCAGAAGAG | 286053 |
rs138427267 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131944 | ATCTGGGCAGCCTGT[C/T]TCCAGAGTCTATGTT | 286053 |
rs138450338 | in-del | -/AC/ACAC/ACACAC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106047 | CGTGTGTGTGTGCAT[-/AC/ACAC/ACACAC]ACACACACACACACA | 286053 |
rs138458319 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250171 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 286053 |
rs138460085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104487 | CCCGAGGGTTCAGTG[C/T]GATAGCTCTACTCTG | 286053 |
rs138473452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224879 | GCCCTTTACTATTAC[A/G]TAAACTGCCTCTTGT | 286053 |
rs138473503 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176862 | CTCTTACCTGGGACT[G/T]GTACCATTACTTCAC | 286053 |
rs138477879 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307512 | AGCCCATTTGTCTGG[-/A]GTGGCAGCAAAGAAC | 286053 |
rs138484041 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292206 | CAATATGTAGATTCA[A/G]GAAGCTATGGGAGGA | 286053 |
rs138521549 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336517 | GCAGAGTCAGAAGCT[A/G]TGAGAGGATGATGAG | 286053 |
rs138522654 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288018 | TCTTGTGGAGACAGG[G/T]TCTCGGTATGTTGCC | 286053 |
rs138525174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171730 | AATAATAATAACAAC[A/G]ATGTGACCATAAGAA | 286053 |
rs138526947 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249045 | GTATGGTGGCACATG[C/G]CTTTAATCCCAGCTA | 286053 |
rs138533607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244644 | AAAAATTTGGGGTGC[C/T]ACTGTTGAATTAGAG | 286053 |
rs138533701 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287148 | GCCAGCCTGGCCAAC[A/G]TGGTGAAATCCCATC | 286053 |
rs138545127 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257789 | TCCGCCCTCTTCGGC[C/G]TCCCAAAGTCCTGGG | 286053 |
rs138571048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283587 | GTGTCTCTAACCAAC[C/T]GGAAACTGCTTAATT | 286053 |
rs138583104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164668 | GAGCCAGTATTATTT[A/G]CTTCTTTAAAACTTT | 286053 |
rs138584354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270492 | AAAACAAGACGAAAA[A/G]CAGAATCTGAATGTT | 286053 |
rs138586812 | snp | A/T | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196148 | CTTGGCCTCCCAAAG[A/T]GCTGGGATCACAGGC | 286053 |
rs138589998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313562 | GAGAAGGACCTCACG[A/G]CTTGCCAGCTTAGCT | 286053 |
rs138649337 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274501 | ACCTACCAGTTTTCA[A/G/T]TTAGACAAGTTTTTT | 286053 |
rs138708104 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342123 | GGACTGCTTCTCAGC[A/C]CTCTATTTCTGTGTG | 286053 |
rs138722066 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344466 | AGATGAATCATGGCC[A/G]GTCACGGTAGCTCAC | 286053 |
rs138741094 | snp | C/T | 0.127944 | 0.218179 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124877 | TCAGCTCACTGCAGC[C/T]TCCACCTCCTGGGTT | 286053 |
rs138761520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118891 | CATTTCATATGAATC[A/G]TAAGTATTTATTCTT | 286053 |
rs138777378 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243714 | TGAGAGTCAGGTAAG[A/G]TGGAGTGAGGGAGGC | 286053 |
rs138814011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148683 | TGACCAGTTCCAGTA[C/T]CAGAATCTAATACTC | 286053 |
rs138817411 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307372 | GGCCAGCCAGCCATC[C/G]TGTTGTCTGTTTCAT | 286053 |
rs138827527 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099896 | GGGAGAAGTAATGGT[-/G]TATTTGTTTGCTGAA | 286053 |
rs138830995 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186671 | AGTCAAAACAGGAAT[G/T]CCATGCCAGTCAACT | 286053 |
rs138882191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232162 | AGTTGGGAGTTCGAG[A/G]CTAGCCTGACCAACA | 286053 |
rs138893686 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357955 | ACTGTAAACATGGAA[A/G]TGGGCTTTCTGGAAA | 286053 |
rs138927640 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327089 | CCAACATGGTAAAAC[C/T]CCATCTCTACTAAAA | 286053 |
rs138928929 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095464 | GGCCAAGTGGTGGCG[C/T]GCGCCTGTGGTCCCA | 286053 |
rs138947797 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144216 | GATTCTCTCCAGTGC[A/G]TGCCTTAGGCTACAG | 286053 |
rs138952937 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226327 | GAAAGGAAGGTGACC[A/C/G]TACAGTTATCAGATG | 286053 |
rs138957481 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237529 | TTAACTCCACTTGCT[A/G]TGCTTCCACACACAC | 286053 |
rs138981641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109239 | ATTCTCTACCCTCCA[A/G]TTTGCCTCAGGTTTC | 286053 |
rs138986212 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366528 | CTCCGTCTCAGAAAA[A/C]AAAAAGAAAGTTAGC | 286053 |
rs139000511 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148031 | ACTACAGTTATCTGA[C/T]GGCACTGCTTCCAGG | 286053 |
rs139011621 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344964 | TCTATACTTCTCCAA[C/T]GTTTCTCTATTATAA | 286053 |
rs139023185 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293069 | CCATGATGACAGTAG[A/C]TGTGCCCCAGCTCTG | 286053 |
rs139032487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160293 | TAAGGTTGCCTAGAA[C/T]GTTCTGTAAAGAACT | 286053 |
rs139070601 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295710 | GTGTGGCTCGGTTGG[A/G]GAATAGTTGGAAGGA | 286053 |
rs139105550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350560 | TTTAATGGACTTAAC[A/G]TTCCACATGGCTGGG | 286053 |
rs139141494 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194243 | CTCCTGTGCCACTTT[C/G]TAGTTGACTCCTCCC | 286053 |
rs139154024 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199056 | TATCATTTTTTTATT[A/G]CGTCTGTATGATTCC | 286053 |
rs139162003 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096901 | AGGCGGGAGCCACCA[C/T]ACCTGGCCCTCTGTG | 286053 |
rs139167074 | snp | A/G | 0.000150463 | 0.0086723 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182300 | GCTTTTTGAAATTAG[A/G]GAACTGACTTGATGA | 286053 |
rs139181130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300879 | CAGAGTGAAGAATGG[A/T]TGGAAGAACATTCCA | 286053 |
rs139187285 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228806 | GCTAAGCTCCTTCTC[A/G]TAAGTAGCTTAGCTC | 286053 |
rs139203702 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111443 | TGATCATCCATAACC[C/G]TATCACCCATCACCT | 286053 |
rs139211268 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116733 | TCTTGAGCTTGCAAG[A/G]CTAGCTTTTCAGAGG | 286053 |
rs139234018 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185651 | AGAGCTTTTGTTCAT[G/T]GGTTATATCAACTGA | 286053 |
rs139235996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132789 | TGTGAGCCACCCACA[C/T]CCAGCCCAATTTTTA | 286053 |
rs139254081 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125127887 | AGCCTGAAGGTAATT[C/T]TATACAACATTTTAA | 286053 |
rs139256400 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255437 | CCTAATCCTTCCTTC[A/G]TCATCAAGGAAGACT | 286053 |
rs139262997 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217277 | CTCCACTGTAATTTT[C/T]AGGGAGTCCTAGAGG | 286053 |
rs139267110 | in-del | -/AC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143108 | GCACGCACACACACA[-/AC]CACACACACACACAG | 286053 |
rs139271917 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177323 | AGATCTGTCTGATCC[C/T]GAGCTCAAAGTTTTT | 286053 |
rs139273968 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180223 | ATATTGCCTTTCTAT[C/G]TTCTCTTTTCCAAAT | 286053 |
rs139274522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362274 | AGCACTGTGGCATGA[C/T]GGCCTTCTCTTATCC | 286053 |
rs139289577 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294318 | TCTCGTGGTATTTAT[C/T]TCACAGTGTAATTGC | 286053 |
rs139294286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263999 | TCATGTCTCAGATAG[A/G]TGGCTCCTTGAAGAC | 286053 |
rs139320918 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298082 | CCTGGCCAACATGGT[A/G]AAACCCCGTCTCTAC | 286053 |
rs139325855 | in-del | -/CTTC | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158709 | TAGATGTCAATTTAA[-/CTTC]CTTCCAACCTCACAA | 286053 |
rs139335350 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204540 | TAATTTTTCCCCGTA[C/T]ACAAAGTATTAAGTT | 286053 |
rs139347702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310901 | ATGTTTGTGATCACT[C/T]GTAATAAAACATTAA | 286053 |
rs139355637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122047 | AGGCCTGTGCTCAGT[A/G]TAGATAGCTCTTTTG | 286053 |
rs139363420 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250966 | GTAAAACAACATGCA[C/T]AATATGATCCTATTT | 286053 |
rs139375011 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255198 | TTCCAGGAGAGCTGC[C/T]CCAGTTAATGCTACA | 286053 |
rs139381383 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354443 | ATCAACAATTAATGA[A/G]GTTAACTTCACATTT | 286053 |
rs139407563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193707 | TGTTGTAAAACAAAA[C/T]AAAAAGCGTATTTCT | 286053 |
rs139439862 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267165 | GGCACGCACTGCCAC[A/G]CCCGGTTAATTTTTG | 286053 |
rs139441246 | in-del | -/T | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196193 | GCAGCCCTGGATAAC[-/T]TTTTTTTTTCTTTTT | 286053 |
rs139453551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304584 | AATTGAGGCTGGGTG[C/T]GGTGGCTCACACCTG | 286053 |
rs139491062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316358 | CCTTCTTGGGAAAAT[A/G]GAACTTCCAGAAAAC | 286053 |
rs139504259 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096177 | TATCAAATGGGAAAA[C/T]GTGGCTTTTTGCAGA | 286053 |
rs139507227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310439 | CATATGATGAGTGCC[C/T]AATCAATTGTAGCTA | 286053 |
rs139507322 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264693 | AGAACCGTGTAAGAG[C/G]TGAAAGACCCAGAGA | 286053 |
rs139528356 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194171 | CATTTTACGGATGAG[A/G]TTCTGCACAATCAGT | 286053 |
rs139543801 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091381 | GAGATTCGGACCAAG[C/T]AGCTGAACGGTGCTT | 286053 |
rs139561722 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250178 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 286053 |
rs139606378 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264238 | GACATTTCTTTTTTA[A/T]TCTTAGCATTTCTGT | 286053 |
rs139631781 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139445 | TAATAAAGACATACC[A/G]GAGACTGGTAATTTA | 286053 |
rs139637124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221245 | ATTAATGCCTTTACA[C/T]AGATGTATCTCTTTT | 286053 |
rs139640522 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188430 | TGAGAGCTTCTGTGC[C/T]ACTGAAAGGGGACAC | 286053 |
rs139653991 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156624 | GTGTGGTTTTTCACT[C/T]GATATGCTAACCTGA | 286053 |
rs139658187 | in-del | -/AG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218437 | TTTTTTTTGAGACAG[-/AG]TCTTGCTCTGTCGCT | 286053 |
rs139662387 | in-del | -/ACTCCCT | 0.0498311 | 0.149774 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179793 | ATCCTCACTGCCCCC[-/ACTCCCT]ACTCAGTCTTCACCT | 286053 |
rs139679097 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280099 | GCCAAGAAAGTGATG[A/T]TTTTCTTTAACACCC | 286053 |
rs139682561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277341 | AGTCAAGGCCATGAT[A/G]TTCATTAGGCACTAG | 286053 |
rs139695873 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149290 | AACCCAGGAGATAGT[C/T]TATGAAATATACTTA | 286053 |
rs139696800 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276750 | AATAACCCAATGAAG[C/T]TAGTGTTATTCCTGT | 286053 |
rs139710104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134865 | CCTGAGTAGTTGGGA[C/T]TATAGGCGTATGCCA | 286053 |
rs139714489 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216013 | GCCATGATTGTGCCA[C/G/T]TGCACTCCAGCCTGG | 286053 |
rs139714861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319802 | TGTTTTAGTGAAGTC[C/T]GGACAGTCTCAAGGA | 286053 |
rs139727390 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201209 | GTCCAGGTTTGTTCC[A/G]TTGCTGGCGAGGAGC | 286053 |
rs139741127 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332831 | TTGACCCTGTGAGAA[A/G]CCGTTTAGTCTTATG | 286053 |
rs139785410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145717 | ACTTTGAGCTCTATT[C/G]AGAAGTAATTCTGCA | 286053 |
rs139785472 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197514 | GATGGTTGTAGATGT[A/G]TGGTGTTATTTCTGA | 286053 |
rs139808185 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115960 | GAAGGGGAAATTAGG[C/T]TCATTGAATTGAAAC | 286053 |
rs139815170 | snp | A/G | 6.60262e-05 | 0.00574532 | missense | NSMCE2 | GRCh38.p7 | 8:125366872 | ACAAGAAAAGACATC[A/G]TCATTCCGAGTAGGA | 286053 |
rs139825241 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212370 | ATTCTGGGGTAATAG[A/G]GGAAGCTCAGGGACT | 286053 |
rs139874457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161595 | CTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCC | 286053 |
rs139880511 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167363 | TGTATTGAGAGTTGC[A/G]TTAAAAGAATTGCAA | 286053 |
rs139881047 | in-del | -/TAAAATAAAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325315 | TAAAATAAAATAAAA[-/TAAAATAAAG]TAAAATAAAATAAAA | 286053 |
rs139890297 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224023 | TTTAAATTTTTAGTA[A/G]AGAGGAGGTCTGGCT | 286053 |
rs139895569 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227773 | ATCACCTGTAATCCC[A/G]TTACCCAGAGATAAC | 286053 |
rs139910876 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299144 | ATTTTTATAGCATCA[C/T]CTACACATAATTTGT | 286053 |
rs139918655 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092082 | TTGTGGAACTTTTCA[C/T]GCCACGGTAGTGAGT | 286053 |
rs139920318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212240 | GAACACATATTCATT[G/T]AAAGGTATCAATAAG | 286053 |
rs139943699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252304 | GAGGCCAAGGGGGGC[A/G]GATCACAAGGTAAGG | 286053 |
rs139944052 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294951 | TCAGTCAAGATTAGT[C/G]GTGGTTCACAGCACA | 286053 |
rs139983793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334020 | GCTCCTGGGTCTGCC[A/G]TGGACTCAGGATAAA | 286053 |
rs140082857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096441 | ATATTTTTGAGGATT[A/C]TTTTTTTCAGTGTAA | 286053 |
rs140087690 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181628 | CATGGCAGGACATTA[C/T]GGAAGGTCAAGGCTA | 286053 |
rs140093788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218205 | TGAGAAAGCAGACTG[A/T]TATTTTTTACTGACC | 286053 |
rs140116572 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173151 | CTTTTTGTCCCTGTT[C/T]TGTGTCATGAGGAGT | 286053 |
rs140121793 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318386 | TCATTCCAGCCTGGG[C/T]GACACAGTGAGACCC | 286053 |
rs140125248 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245079 | CTGAGGTCAGGAGTT[A/C]AAGACCAGCCCGACC | 286053 |
rs140125396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323314 | TTATTCTGAAATTCC[C/T]ATAGAAACACAGAGG | 286053 |
rs140125530 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102341 | TCAAGATGCCAGGAC[A/G]TTCCAGTTCAAATTC | 286053 |
rs140127458 | in-del | -/TG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298691 | TCATCTGTGGGTTTT[-/TG]TTTTTGTTTTTTTTT | 286053 |
rs140128901 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111859 | TCAATACAACTGACC[A/T]GATATTTTCAGGGCT | 286053 |
rs140132062 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242562 | CAAGAACTGTTAGCT[A/T]ATGGTTCATCCCATG | 286053 |
rs140138568 | in-del | -/TTTTA | 0.163564 | 0.234582 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117539 | TTATACCTTTTTTAT[-/TTTTA]TTTTATTTTTTTAAG | 286053 |
rs140152680 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315481 | CAAAACCTCAGTTTT[C/G]TCATTTATGAAATGG | 286053 |
rs140160236 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361314 | CTCAAGTGATCTGCC[C/T]ACCTTGGCCTCCCAA | 286053 |
rs140191602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355768 | ACAAGTATCTTTTCT[C/T]CAGAGAGAATGGCTT | 286053 |
rs140212349 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215899 | ACCAGCTTGGGCAAC[A/G]TAACGAGACCCTGTC | 286053 |
rs140215265 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176234 | GGAGTCAGCCTTTGC[A/G]CATATGTCTGCTCTT | 286053 |
rs140223134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254247 | AAACAAAAGTCTTTT[A/G]CATTTTTCATATTCT | 286053 |
rs140242813 | in-del | -/AGAA | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093742 | AATAAATAAATAAAT[-/AGAA]AGAAAACTGAAGAGA | 286053 |
rs140246169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150731 | CCAAATAATCTAGCT[C/G]TGTGTTATTAAAAGT | 286053 |
rs140257249 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290937 | ACCATAATTATGTTT[A/G]ATTCTCTAGTACCTA | 286053 |
rs140283424 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356244 | TATGTCTGTGTGTAT[-/G]GGGGGGGGGTGTTCT | 286053 |
rs140300496 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271132 | CAGGCATGGTGGTGC[A/G]CACCTATAATCCCAG | 286053 |
rs140344737 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229392 | TGTATCCCATACAAA[A/G]TTTTTAATATTTTAA | 286053 |
rs140345661 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286382 | CAATGGTGCAGTCTC[A/G]GCTCACTGCAACCTC | 286053 |
rs140347698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213311 | ACAGGAAACTAGTCA[C/T]ATTATTAATTGCATT | 286053 |
rs140364690 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267420 | GTAAGGCTAGACAGT[C/G]AGGACCAAATGTGAG | 286053 |
rs140376255 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256487 | CTGGCATCCATGTAG[C/T]GATGTCAGTGAGGCA | 286053 |
rs140382393 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125004 | TTCACTATGTTGGCC[A/G]GGCTGGTCTGGAACT | 286053 |
rs140419944 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102469 | TCTAGTGTTGCTTTG[A/G]ATCTTGTGGAAAGTC | 286053 |
rs140423860 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163544 | GGGGTAATAATAGTA[C/T]TTGGCCTACATACCT | 286053 |
rs140473172 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195567 | CATATCTCAGAGCCT[C/T]ATTTTGAAACTCGAT | 286053 |
rs140484482 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269435 | TATGGCTGATTTGGT[C/T]TTTGAAATACTGTTT | 286053 |
rs140495994 | in-del | -/TG/TGTG/TGTGTG | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129544 | GAAAAGATTTGGCTC[-/TG/TGTG/TGTGTG]TGTGTGTGTGTGTGT | 286053 |
rs140505048 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351633 | AAAATTTTGTAACCT[C/T]TTTACTAAAGATTAA | 286053 |
rs140510235 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273594 | TTTAAAACTACCTTT[A/C]CAACTTACAGTTTAT | 286053 |
rs140538471 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250187 | TAGAGATGGGGTTTC[A/T]CCATGTTGGCCAGGC | 286053 |
rs140551087 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312349 | TGTGTATTGTGGCCG[A/G]GCATGGTGGCTCATG | 286053 |
rs140567305 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307818 | AGTTAAAAACGATTA[C/G]TGTGGTCTCAGAGGA | 286053 |
rs140577000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185855 | CTCTTCAATTTTTGG[C/T]TTATTTAAATAGAAG | 286053 |
rs140580631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302918 | CTGGGAATCCGGGAC[A/G]AAGAATCTGAGCACA | 286053 |
rs140596648 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231243 | CCTAATACACAGAAA[C/G]TGCTGTGCCACATAA | 286053 |
rs140622830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113427 | CAAGGCTACAGCAAG[A/G]TATGATTATACCACT | 286053 |
rs140623528 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155384 | CAGCTTCAGAGTGCC[C/T]TAATCAATCCAAAGA | 286053 |
rs140623927 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101493 | GATTCCATGAAAATA[C/T]CCCTTTTTCTGCTGC | 286053 |
rs140661455 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130698 | TAATGTATGTGTACA[C/T]ACATACCTGTCACTT | 286053 |
rs140664534 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173322 | GGTCATTAGGTGTGA[A/T]GAGGGGGAGGAGAAG | 286053 |
rs140684783 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152357 | CTTTCAATTTCAGCC[A/G]AACCCTAGAACCAGC | 286053 |
rs140692089 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355700 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs140701581 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251413 | CTTAATGGGAAGACA[A/G]TGATTTTTAAATGGG | 286053 |
rs140704637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148069 | TGATCCTCAGTTCTT[C/T]TTAGAATTTCCTTCC | 286053 |
rs140713336 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289099 | TTGGCCTTTTCCCCC[A/T]GTCTTTAATTCATCT | 286053 |
rs140715313 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246335 | ATTACAGGCATGCGT[C/T]ACCATGCCCGACTAA | 286053 |
rs140739282 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365316 | GCTCCACAGCCACTC[C/T]ATCGGCAAGTCCTAT | 286053 |
rs140747894 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257678 | AGCTGGGACTACAGG[C/T]GCTCACCACCATGCC | 286053 |
rs140747975 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179021 | CCCTGCTTGGACTTG[C/T]CCTGATCTTGGACTT | 286053 |
rs140755958 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297434 | CATTTTCAAATAGTT[A/C]TAAATGGGGGAAATG | 286053 |
rs140779336 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286127 | GCCCCTTCTCAGGAT[C/G]ACAAGACTACCAGAA | 286053 |
rs140785968 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108110 | CCCAGAAGAAATTAC[A/G]ATGAAAATAGTTTTG | 286053 |
rs140804833 | in-del | -/AT | 0.423881 | 0.179625 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353902 | ACTAAAAAATAAAAA[-/AT]ATATATATATATATA | 286053 |
rs140805129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124402 | ATTGATCATGCTTGC[A/G]TTCTGAAACTGCTGA | 286053 |
rs140810281 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208016 | CTGCTTCTTGATGGG[A/T]GGGTGGTAGAAAATA | 286053 |
rs140836085 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330278 | ATCTCCCGGTTCGAG[C/T]GATTCTCCTGCCTCA | 286053 |
rs140850499 | snp | A/G | 0.164873 | 0.23506 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326072 | ACCATCCTGGATAAC[A/G]TGGTGAAACCCCATC | 286053 |
rs140947152 | in-del | -/AAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313252 | AAAGAAAGAAAAGAA[-/AAG]AAGGAAAGAAAAAAG | 286053 |
rs140950402 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127330 | TGAGGTTGGGGGAGT[A/G]CATGATAGTAAGGGC | 286053 |
rs141001460 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312657 | AATAAATAAATAAAT[A/G]TGTTGCATCTGCAGT | 286053 |
rs141036539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122921 | TTTCACTCAAAAGCA[A/G]CCATAAACAATATGT | 286053 |
rs141038783 | snp | A/G | 0.0019964 | 0.0315312 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177012 | GTTGCAGACTTCTCT[A/G]TTTTTTGCCCTAGTA | 286053 |
rs141056901 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174834 | TTAAGTGTTTTGTCA[A/G]AAGTCAAAACCATGC | 286053 |
rs141068376 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143655 | AGACATGCCTGTACA[C/T]GGCTTTGTAGAATAA | 286053 |
rs141075123 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290605 | TTAGAATCTCTCAGT[C/T]ACAATTCCAGTCTCA | 286053 |
rs141075801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141584 | AGGTAATAGGTGCAG[G/T]GTGCCTGGCACAGAC | 286053 |
rs141076564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265588 | ATTCAGTTTTTTGTT[C/T]TTTGTACCCTCTTAA | 286053 |
rs141088166 | in-del | -/TTAA | 0.0502101 | 0.15028 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222243 | ATTTTTTAAAATTTT[-/TTAA]TTGAGAAATAATAAT | 286053 |
rs141093631 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217501 | GAGTAGCTGGGACTA[C/T]GGGCACCTACCGCCA | 286053 |
rs141110358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306971 | TATATAGAGTAAGCA[A/G]TTTATAAAGGTTCAA | 286053 |
rs141111188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157736 | AGACTGATTTTCACC[A/G]TTACCTCATAGAAAT | 286053 |
rs141170407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189137 | AGATAATCAGTGTCA[C/T]GAAGAAAAGTCAGCA | 286053 |
rs141208030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185215 | CCTAGGTACACTCTG[C/T]TGGCAGTGCACCAGC | 286053 |
rs141208611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315195 | GAGTGGTAGGGACAG[A/G]AGAAGTAGATAGGTA | 286053 |
rs141265587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227800 | TAACCACATAATAAC[A/G]TTTTGTGGTTTCTTT | 286053 |
rs141299849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199521 | ATCCTGAGTTCTAAT[G/T]TGATTGCACTGTGGT | 286053 |
rs141313730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247465 | AGATTTGGCTCACGC[C/T]TATAATCCCAGCACT | 286053 |
rs141315559 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250145 | CAGTCATGCACCACC[A/G]TGCCTGGCTAATTTT | 286053 |
rs141332813 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159890 | GCTTGAACCCAGGAG[G/T]CAGAGGTTGCAGTGA | 286053 |
rs141348664 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266703 | CAGTATACCTGTTGG[A/G]GATGAATAGCAAAAG | 286053 |
rs141367915 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108893 | GAACATTGATGGCCT[A/G]TAATGTGATGCTTTG | 286053 |
rs141371167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278274 | ATTCCTGCGGAGATA[C/T]TGAGCAATCTTTGGG | 286053 |
rs141373061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194474 | TCGCATGGATATACC[A/G]TAGTTTGTTTATTCA | 286053 |
rs141380961 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243861 | TTACAGCTTGCTGAG[A/G]CATCTTTTCTTCAAA | 286053 |
rs141384116 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311400 | CTCCAAAGAAGGAAA[C/T]CTTATTTTTACCTTG | 286053 |
rs141400759 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177016 | CAGACTTCTCTATTT[C/T]TTGCCCTAGTACTGG | 286053 |
rs141415167 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250150 | ATGCACCACCATGCC[C/T]GGCTAATTTTTGTAT | 286053 |
rs141420258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219112 | AATCTACTTTAATGG[A/G]ATAAACTTTTAAATG | 286053 |
rs141431514 | in-del | -/TTTTGTTTTGTTTTGT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314278 | TGTGTTTTGTTTTTG[-/TTTTGTTTTGTTTTGT]TTTTGTTTTTTGAGA | 286053 |
rs141435797 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364087 | TAGCTGGGATTACAG[C/G]CATGCGCCACCACGC | 286053 |
rs141447682 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235659 | CATGTCAGTGAATAC[A/T]AAGAATTGTGTTTAA | 286053 |
rs141453077 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104976 | TGCAGTGAGCCGAGA[C/T]TGTGCCACTGTACTC | 286053 |
rs141458533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153641 | AGCCCTGGTTCTTCT[A/G]CTTTCTAAGTTATGA | 286053 |
rs141488955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119171 | CTCACCTCCTGTTAC[C/T]GTGGAATCTCACTCC | 286053 |
rs141539966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287485 | GATTGCTCTCCTGGC[C/T]AGAGATAACCAGAAG | 286053 |
rs141543071 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098606 | GTGTTATCAGCAGAA[C/T]TGGTGAGAGTGGTTG | 286053 |
rs141575063 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249723 | CAAGCAAGAATACTC[A/G]GTGCTTATGTGGGCA | 286053 |
rs141581477 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172453 | TTACAAATATAGTGG[C/G]AGCAACAACAAAATG | 286053 |
rs141589337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244845 | GAACATTCGCACACA[A/G]AAAAAGATATAGAGG | 286053 |
rs141590775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206905 | GGGAGAAGAAGAAGA[A/G]GCAGAGCCAGCAAGG | 286053 |
rs141629425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201925 | CACCGTCCCCCACCC[C/T]ATTCCCCCGCCTTCC | 286053 |
rs141645230 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366069 | CGCTTCATTCTGGGT[C/T]CTGCCCTAGATAAGA | 286053 |
rs141657518 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283879 | CTCAAGTAGGCCGGG[C/T]GCAGTGGCTCACGCC | 286053 |
rs141669996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117806 | ATCTGATGTCTTCAG[A/T]GTCTGGGACTTTAAT | 286053 |
rs141674214 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121163 | TTAGTTGGAAAAGCT[A/G]TATATACATGGTGAG | 286053 |
rs141677251 | in-del | -/TTCCTGCCT | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094046 | TGGCCTCAAGCAATC[-/TTCCTGCCT]TGCCCTTTCAAAGTG | 286053 |
rs141684549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353606 | AATATCGTTTTAGGA[C/T]GGGTGCAGTGGCTCA | 286053 |
rs141693816 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250627 | TCATATGTCTCTTGC[A/G]GACATTTCTTCGGAT | 286053 |
rs141707107 | in-del | -/T | 0.323908 | 0.238825 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192330 | TTCATTTTTAAAAGG[-/T]TTTTTTTTTTTTTTA | 286053 |
rs141728271 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264890 | TCATTTAATCTTCAC[A/G]ACAACCCTGGGAATG | 286053 |
rs141762780 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232293 | GCTTGAACCCAGGAG[A/G]CGGAGGTTGTGGTGA | 286053 |
rs141777145 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115773 | CTTTCATGGCCATTA[A/G]TATATTGTTTAGTCT | 286053 |
rs141777661 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300383 | GCCCAGGCTGGTCTC[A/G]AACTCCTGAACTCAA | 286053 |
rs141786582 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335638 | GAAAACCACACAAGC[C/T]CTCTCAGTGTTCTGA | 286053 |
rs141790554 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348600 | ACTGAATCATGGGGG[C/T]GGTGTCCTCCCTACT | 286053 |
rs141800944 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244276 | GATAAAGAAAGTTCA[A/C]AGTTGAGCAGTAGCA | 286053 |
rs141822678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134463 | ACTTTTAGCCATTCT[A/G]ATAGATATGCAATGG | 286053 |
rs141842483 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181526 | AAATTTATAATATTG[A/G]GAAATAATTTTATAA | 286053 |
rs141884432 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195855 | AAAGTTTATGTTAGT[C/T]ATTACATTCTTTTTC | 286053 |
rs141925457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126961 | ATTATTTGGTTCTTT[C/T]GCAGGTGAGAGAGGT | 286053 |
rs141932299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211820 | TTCATATTGTTTGCT[A/G]TCCTTTAGAATATTT | 286053 |
rs141958395 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327287 | AAAAAAAAAAAAAAA[-/G]AGAGAGAAACCAAAA | 286053 |
rs141959159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139188 | CTTTTTAGGAAATTT[C/T]ACATGGAGTAGAAGT | 286053 |
rs141966422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255048 | TTAAGAACCTAGCAG[C/T]GTCCACTTCCTGTCT | 286053 |
rs141971083 | in-del | -/TCTCCTCTCCTCTCC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213486 | CCTAAGGCACCCATG[-/TCTCCTCTCCTCTCC]TCTCCTCTCCTCTCC | 286053 |
rs141997624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146390 | TAAAATGGAAATAGA[A/G]CTACCTAACTCTTTA | 286053 |
rs142046363 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223852 | GGTCTTGCGCTGTCA[C/T]GCAGGCTGGAGTATA | 286053 |
rs142055663 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303843 | AATTTCATTGCATCA[A/G]GTGTGATTGTAGTGT | 286053 |
rs142064495 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125151271 | TGTTCAATCTACAAT[A/C]AATCATGTAAGTTTA | 286053 |
rs142085389 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341155 | AACTGGAGAGCTGCA[A/G]TCCAGCCTTGTCCTT | 286053 |
rs142112081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197985 | ACTCATGATTTGGGT[C/G]TCTGTCTGTTATTGG | 286053 |
rs142119790 | in-del | -/ATA | 0.179425 | 0.239831 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171709 | CATCTTAAACTTGCT[-/ATA]ATAATAATAATAATA | 286053 |
rs142147427 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240022 | TGAGGGTCAGGGTCT[A/T]AACAGAGATTCACTG | 286053 |
rs142147439 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281583 | TAGCTGTAATTACAG[A/G]AGTGCGCCATCACAC | 286053 |
rs142151289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329110 | TGCAGCAACATCAAG[A/G]TAGGACCTCATGCTT | 286053 |
rs142168389 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145306 | ACAGCCCTGGCACTG[A/G]CATACTTACAGAAAC | 286053 |
rs142173304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318555 | CCAAAAGTATGTATA[C/T]AGTGATGTTAATGGC | 286053 |
rs142181288 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245261 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 286053 |
rs142181646 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256044 | ATCCCAGCACTTTGG[A/G]AGGCTGAGGCAGGTG | 286053 |
rs142204052 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357649 | AGCTCAGGACTAGGA[C/G/T]GAAACAGCTACTGGA | 286053 |
rs142208068 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277866 | CTGAGAAATCATAGA[A/G]AACTGTAAATTAAAT | 286053 |
rs142236252 | snp | A/G | 0.000631439 | 0.0177573 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366737 | TTAAGGCAGTAAAGG[A/G]GACTGACTTGATGTT | 286053 |
rs142254336 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091031 | AGCTCCATGCGCTTG[A/C]AATCAGGAGACCCAG | 286053 |
rs142315892 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166137 | TTGAAATCAGACTTA[C/T]TATTTATTAGAAAAG | 286053 |
rs142316112 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117690 | CCAGCTAATTTTTTT[A/G]TTATTTTTAGAGACA | 286053 |
rs142348550 | in-del | -/A | 0.0244538 | 0.107838 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099841 | GGGGCTGGTAACCAG[-/A]GGGGTAAGTGGGAGG | 286053 |
rs142356170 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210216 | AGATTCAATGAATTT[A/T]TATATGAAAGTCATT | 286053 |
rs142356230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160449 | AAGGGCCTCTTTCCT[C/T]GGAAGGGGTTGGGGG | 286053 |
rs142366681 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250112 | CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGGTAC | 286053 |
rs142367554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114096 | ATAAATATTTTGCCC[A/G]GTATGTCTAGGCCCT | 286053 |
rs142368781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213239 | GAAAGCAAAATGAAT[C/T]GTGCCATTGGAAAAT | 286053 |
rs142394894 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243386 | TTTAAAGGGCCTTAA[G/T]CTGAAAGATGTTCCA | 286053 |
rs142411288 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102393 | CTTCAGTGGTGTAGA[A/G]TCTGCTCTCTCCTCC | 286053 |
rs142447185 | snp | A/G | 4.96997e-05 | 0.00498472 | missense | NSMCE2 | GRCh38.p7 | 8:125357803 | AGTCCAGGCAAAAGC[A/G]GAAGAAAAAGGCCTA | 286053 |
rs142451552 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268913 | GGAGCAAGAGTATCA[A/C]AAAGTAGGAATTTTA | 286053 |
rs142451898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362993 | ATTCACTGTCTGGCT[A/G]TGAAAGTTAAGGCCT | 286053 |
rs142453564 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162794 | ACTTGGAATAAATGG[C/T]GATAAACTTTCCTTA | 286053 |
rs142462680 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280625 | TAATTTAAAAAAGAA[A/G]GTATTTGAAGTCCAG | 286053 |
rs142471685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324280 | AAAGTTAAACATATA[G/T]GACCTAGGCATCCCA | 286053 |
rs142474035 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206040 | GAAACTTGGGAAACA[A/G]TCAAGAGCTTTGTGA | 286053 |
rs142494785 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296284 | TATTGAATGAATACT[A/C]TGTTTGTAAGAGAGA | 286053 |
rs142511311 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107327 | GAGTCCTGAGTAGCT[C/T]GGATTACAGGTGCAC | 286053 |
rs142513090 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302035 | CACAATCTCAGCTCA[C/T]TCAAATTCTGCCTCC | 286053 |
rs142520826 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223705 | CTTCGTGATTTTAAT[G/T]TGCATTTCCCAGGTG | 286053 |
rs142530546 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338134 | GAAAGGTGGTATACA[G/T]GATGTGACCTCCCAG | 286053 |
rs142537534 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237954 | CCATGACAGTTGACC[C/T]CTTCTGGGTGAATAT | 286053 |
rs142541014 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224897 | AACTGCCTCTTGTTG[A/G]TTGACTTTATTGAGG | 286053 |
rs142554991 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229339 | GTCTCAACTTTTTTT[-/T]AAATCACACATCCTT | 286053 |
rs142557393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155871 | GGGGGTAGTCCTTGC[A/T]ATGTTTTTCTAACCT | 286053 |
rs142576906 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298008 | TGCAATGCCTGTAAT[C/T]CCAGCACATTGGGAG | 286053 |
rs142590041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341781 | TCTCTGGGTCTTGCA[A/G]AGCACTCCTTTACTC | 286053 |
rs142595390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264127 | GTCCATGAGGGAGTC[C/T]CTCCCTAGAGTAAGC | 286053 |
rs142602692 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290085 | AAAATGGGGAACTTC[C/T]AGACAAGCACCTGAG | 286053 |
rs142621697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188278 | ACCACAGTGTAGTTG[A/C]ACAAGGGTAGTGGTT | 286053 |
rs142641406 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101333 | TACTACACAGTTCCC[C/T]ACTTAGGAAGGGCAG | 286053 |
rs142692986 | in-del | -/A | 0.0547245 | 0.156101 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131606 | TGAGTTCTAACGTGG[-/A]AAAAAAAAAATGCTT | 286053 |
rs142725361 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099023 | GATACATAGTATTAC[A/G]TTCATTCCTTCTTTC | 286053 |
rs142746737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349373 | TGGGCAGCCTAATAA[A/G]CATTTCAAGCAGGCA | 286053 |
rs142770014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231570 | CACTTTTGCACACTA[C/T]AGATTGCAACCCACA | 286053 |
rs142810419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096191 | ATGTGGCTTTTTGCA[A/G]ATTAGGCCTGGAAAT | 286053 |
rs142814371 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148555 | ACTTTTGCTCCCAAC[A/G]GATACTTTAGTGAGT | 286053 |
rs142838088 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144802 | TTTAAGTTGAATTTG[A/C]TTATAACACAAAATC | 286053 |
rs142845829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227278 | GGTAGCTCGGTGTCT[C/T]CATCAGTGGTAGCTG | 286053 |
rs142864670 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343867 | AAAAATTAGCTGGAC[A/G]TGGTGGCGGGCGCCT | 286053 |
rs142867925 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123965 | AGAATATTCAGAGAT[A/G]TATAACCATCACCAC | 286053 |
rs142874557 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266376 | AACTATGAATTCAGT[A/G]GCATGTCTTATAAAG | 286053 |
rs142877289 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252449 | GAGAATGGCGTGAAC[C/G]CAGGAGGCGGAGCTC | 286053 |
rs142880923 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316633 | TTTCCTTCTTTCCTT[C/T]CTTTATTTCCTTCTT | 286053 |
rs142883947 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193271 | TTAAGGTAGTGAATG[C/G]ACAAGCTACAACATA | 286053 |
rs142886273 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174767 | ACAACACCTTGGCAA[A/G]CCGTGAAGTCCACTT | 286053 |
rs142891049 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314215 | TTATGCAAATCCCAT[A/G]AATCAGTAATGTGCT | 286053 |
rs142904846 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309180 | CTTGAACCTAGAGGC[A/C]GAGGTTGCAATGAGC | 286053 |
rs142915036 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237657 | TAATAAAGTCACATT[A/C]TTTTTTTCTCAGTAC | 286053 |
rs142924472 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360643 | GCAGGGTTCTGAAGG[C/T]CAGGTGCATTTGGGC | 286053 |
rs142927398 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161792 | GTGAGACAATGTCTC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs142967531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306234 | TCTCGGGAGGCTGAG[A/G]CGAGAGGATGGCTTG | 286053 |
rs142969946 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117508 | CGTTTTCTTTGTTCC[A/G]TGGGGCTTTTTGCAT | 286053 |
rs142977726 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318881 | AATGGAGGAAATATA[A/G]CTAAGAGTCCAGGGA | 286053 |
rs142983007 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246152 | AACTCTGTGACAATT[C/G]AATCTGCAAAATGAA | 286053 |
rs142987661 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280160 | TGATTTTTTAAAGCT[G/T]CCTTTATTAACATAA | 286053 |
rs143065139 | in-del | -/AG | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363543 | GAAAGAAAGAAAGAA[-/AG]AGAGAGAGAGAGAGA | 286053 |
rs143080185 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254684 | GCTATAAGACTTTAA[A/G]CCTAATTTCCTTTGA | 286053 |
rs143095270 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143144 | GGTGCATGTATAGAT[A/G]TGTGTTGCTAGAGAT | 286053 |
rs143100484 | snp | A/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176826 | CTGGCAGCAGACATC[A/G/T]GCAGCTGAGTAACAG | 286053 |
rs143131581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334598 | GAATTGTTTTTCTCA[C/T]GGGTTGGAATGTAGC | 286053 |
rs143162302 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203051 | CATGAATATTTGTTA[C/T]AAGCAAATGAAATGG | 286053 |
rs143169857 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137808 | AAGGTACTTAACCTC[G/T]CTGAGCCTGTATTTT | 286053 |
rs143183554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118494 | GTTCCCAGGGTCTGC[A/G]GGTACACTTTGAGAA | 286053 |
rs143187629 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249000 | CATGGTAAAACCTTG[A/T]CTCTACTAAAAATAC | 286053 |
rs143198933 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136243 | AGAAAGAGAATTGGC[A/C]ACATCATGGAAGAAC | 286053 |
rs143208899 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322826 | AATCAGAATTTAAAA[A/T]TTTTAAATGCCATTT | 286053 |
rs143216843 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337472 | TTAATATTGGTCATA[A/G]TGAAACATGTTTTCA | 286053 |
rs143245876 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153317 | ATCAGGAAGGTCTCT[C/G]TTCTTTTATAGGAAG | 286053 |
rs143256358 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111756 | AGCGAGCCGAGATCA[C/T]GCCACTGCACTGCAA | 286053 |
rs143271566 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258301 | AGAGTAGTCTTTTAA[A/G]AAAATGGAAACAAGG | 286053 |
rs143282449 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272822 | ACACACGTATATATA[C/T]ACACATATATATACA | 286053 |
rs143288936 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242132 | TGAGAACCACTGTTA[A/C]AGGTGACAGTTGAAG | 286053 |
rs143310623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212288 | CTGGTAGCCCAGGAT[A/G]GAGTCTTTCTGGGTT | 286053 |
rs143314902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331914 | ATATGGCCTGTGCAA[A/G]GGCAAACAGTAGTTC | 286053 |
rs143334241 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255289 | AAAATAAATGACTGT[A/T]GAGTTAAGCCATAGA | 286053 |
rs143353757 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230223 | GATATCTTTACAAAA[C/G]GCTCATGCTTTTCAG | 286053 |
rs143356760 | in-del | -/CC | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235449 | AGATAACTCCTCTGA[-/CC]CCAATCCCAGTTTGT | 286053 |
rs143359332 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306373 | TTAAAAAAAAAAAAC[-/T]GAGCAACAGCTGTTT | 286053 |
rs143392455 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197581 | TTGGTACCAGTATCA[C/T]GCTGTTTTGGTTACT | 286053 |
rs143403170 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250133 | TAGCTGGTACTACAG[G/T]CATGCACCACCATGC | 286053 |
rs143450514 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314819 | GCTCTTGGTGATAGA[A/G]CAATTAAGTAAAATG | 286053 |
rs143474263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295069 | ACTTTCTTGAATGTC[A/G]TGTTGCTGTGATGAC | 286053 |
rs143488031 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290619 | TTACAATTCCAGTCT[A/C]ACAGAAAAGTTGGTT | 286053 |
rs143511720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098463 | GTCACATGATCTTAC[A/G]TACATTTTCAAAGGT | 286053 |
rs143518950 | in-del | -/C | 0.0792508 | 0.182605 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284475 | CCAGAGAGGTTCTAT[-/C]CCTTATCGAGGATTG | 286053 |
rs143520867 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217908 | ACCAAAACAAAAACC[A/G]TTGTACTAGGATAGA | 286053 |
rs143521006 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214410 | GAGCATTAAAGGAAT[A/G]AGATCAGAATTGGCA | 286053 |
rs143523251 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287403 | GCTACAAGCCCAGTG[C/T]CATTGTTTCATGCCT | 286053 |
rs143548965 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355867 | TTCAGTTGGGGGCCA[A/G]TGGGATGTAACTCAA | 286053 |
rs143560396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115488 | GGGCTCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 286053 |
rs143579412 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164841 | AATAATAGCAAGCCT[A/G]GCTAACATGTCTCCA | 286053 |
rs143597053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244016 | AGAACTCAAGAAAGG[A/G]AAGATATTGTAAGAG | 286053 |
rs143603523 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282544 | TCCACTTACTCCTTC[G/T]ATTTAAGAGTTAGAA | 286053 |
rs143619646 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178818 | GAGCTTGCAGTGAGC[C/T]GAGATCGTGCCACTA | 286053 |
rs143630476 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154800 | TCACTATTACTGCCA[C/T]GGAAAAACTGTTTTC | 286053 |
rs143635873 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298451 | GTAAACGTGAGATCC[A/G]GCGTTTGCAGTCAAG | 286053 |
rs143643845 | in-del | -/AAAT | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248041 | TGGCTCATTCAATAA[-/AAAT]TTTGAAACCATTGAT | 286053 |
rs143663800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110656 | GACTTCATAGTTTCT[G/T]CCCTTCACCATTACA | 286053 |
rs143684304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273906 | TCATCTGCATACCTC[C/T]TGCTGGGACCTGGAG | 286053 |
rs143685021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134872 | AGTTGGGACTATAGG[C/T]GTATGCCACCATACC | 286053 |
rs143700076 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312396 | TTTGGGAGGCTGAGG[C/T]GAGTGGATCACAAGG | 286053 |
rs143704652 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239962 | CTGCCCCTTCTTGCT[C/G]ATTGCTGAGGCCACT | 286053 |
rs143712812 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259582 | CGGCCCCTGGCACCA[A/C]AAGTTGGAGACAACT | 286053 |
rs143725805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128865 | TCCACCCAGATAAGC[C/G]TGGATTCTCTCCCCA | 286053 |
rs143745257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291891 | TAGATTTTTTTCCTA[C/T]ATAAAGTTCAGTGCA | 286053 |
rs143768704 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116831 | TCACTATATGGGCCA[A/G]TGGCCATACTGAAGA | 286053 |
rs143773721 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190399 | TAGTGAACAGTAGAA[C/G]CAGAAGACAGACGGT | 286053 |
rs143782007 | in-del | -/TG/TGTG | 0.0562865 | 0.158292 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203231 | ACTTATCGTAAATGT[-/TG/TGTG]TGTGTGTGTGTGTGT | 286053 |
rs143802032 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250173 | TTTTGTATTTTTAGT[A/T]GAGATGGGGTTTCAC | 286053 |
rs143860301 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332460 | AATAATATAGTACTC[G/T]CATCAGAGTTGTATC | 286053 |
rs143863447 | snp | G/T | 0.301681 | 0.2446 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197722 | GTTTTTTCCAATTCT[G/T]TGAAGAAAGTCATTG | 286053 |
rs143881827 | in-del | -/CTGAAAGACAGAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284254 | TTAAAAAAAATACCC[-/CTGAAAGACAGAG]TATGTCTTCGACTCT | 286053 |
rs143884693 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314901 | GCAGAGAAGTAAACA[A/C]AGCGAGATGTTGGGT | 286053 |
rs143887983 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315726 | GAAAGAGTATGACTT[C/T]TTAGCAATTATATTT | 286053 |
rs143898275 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242656 | TCAGCTTACAACAGC[A/G]GGAGCTAGAGACCTG | 286053 |
rs143902202 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361742 | GGTTGTTAAGACCGA[C/G]GCTGATAGAGTTGTT | 286053 |
rs143902556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311557 | GTGGTATGTTGTGCA[A/G]TATGTCAGCATTTCC | 286053 |
rs143911332 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126170 | GGCAGATCACTTGAG[A/G]TCAGGAGTTCGAGAC | 286053 |
rs143942485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241464 | CTTAGGGCATCAAGA[A/G]ATTCTCCTTACAGTT | 286053 |
rs143948744 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094835 | AGAGCAGTCCCTGGC[A/G]TCTCTTCCTTTTCTT | 286053 |
rs143956757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179982 | GAATGTCTTCCTATA[A/C]TGTTACCATTAACAT | 286053 |
rs143972366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359912 | GAAGTTACTCCAATA[A/G]CAATGCAGAGATGGA | 286053 |
rs143999467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266450 | TAATGAAAATAGTTC[A/G]TAACAAGAACAAACA | 286053 |
rs144015922 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192627 | GTCATACAATTTTAC[A/C]CATTCAAATAATACT | 286053 |
rs144045603 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292352 | TTGAGGTCAGGAGTT[C/T]AAGACCAGCCTGGCC | 286053 |
rs144059176 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200937 | CTTCAATCACTGATA[G/T]CATTTCTTCCAGTTG | 286053 |
rs144080929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139621 | CATCAGATCTCATGA[A/G]ATTTATTCACTATCA | 286053 |
rs144100923 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135741 | TATATCCATTTCTGG[A/G]CACAATTCAATGCTG | 286053 |
rs144106234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217288 | TTTTCAGGGAGTCCT[A/G]GAGGTCTAGAGATCT | 286053 |
rs144112001 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288562 | TCCTGGTCCTTTTTC[C/T]TGGCAAATCTCTGTA | 286053 |
rs144112013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336677 | TGTGTGGCATTTTAC[C/T]ACCTGGTATATGGAA | 286053 |
rs144113222 | in-del | -/GGCAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161726 | GCTTGAACCCAGGAG[-/GGCAG]GGTTGCAGTGAGCCA | 286053 |
rs144116993 | snp | G/T | 0.121022 | 0.21416 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309031 | GGGTGGATCACCTGA[G/T]GTCAAGAGTTCAAGA | 286053 |
rs144124930 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215945 | TGTTGGCACACACCT[A/G]TTGTCCTAGTTACTT | 286053 |
rs144147194 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260045 | GATATTCTGGGATAA[A/G]TATTTTATTTAAAAA | 286053 |
rs144150868 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330095 | CAGGTAGCTTTACAG[A/G]TTCGGGGCACGTCGC | 286053 |
rs144154887 | snp | G/T | 0.0607341 | 0.163335 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256699 | GGGAGGCCGAGGCGG[G/T]TGGATCATGAGGTCA | 286053 |
rs144172161 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101560 | AACTGTGAATTCTCC[C/T]CACTTTTCTAGTTGG | 286053 |
rs144207060 | in-del | -/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249970 | GGAAACAGTATTTTA[-/TT]ATTATTTATTTGTTT | 286053 |
rs144209345 | in-del | -/AC | 0.0170251 | 0.090679 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209410 | CCTTTCCTAAATTTG[-/AC]AGGTAAATTTGCTTT | 286053 |
rs144216283 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184986 | AGTAAAGGCTGAAGT[A/G]CTTTTATGGTCTACA | 286053 |
rs144227812 | in-del | -/TG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208131 | ACATCATTGACTGTA[-/TG]TGTGTGTGTGTTTCA | 286053 |
rs144228581 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304734 | TGGTAGCATGGGCCT[G/T]TAATCCCAGCTGCTT | 286053 |
rs144244755 | in-del | -/TAGT | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179486 | GAAACCATTAAAAAA[-/TAGT]TAGTGCCCATTTGTT | 286053 |
rs144274171 | snp | A/T | 0.00716266 | 0.059414 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091919 | GGTCTAGGCAGGGGA[A/T]ATTGGGGTGCCACCA | 286053 |
rs144290852 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250127 | CCCAAGTAGCTGGTA[C/T]TACAGTCATGCACCA | 286053 |
rs144293849 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301516 | CTTATTCACCGAAAG[C/T]ACTTGGAAGACTTTC | 286053 |
rs144294513 | in-del | -/CTGA | 0.0310518 | 0.120672 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129633 | TTGCTGGAATGATGT[-/CTGA]CTGGTGCCTTATTTA | 286053 |
rs144307876 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255915 | CCTAAATTAAGACTG[C/T]GAGGGTGAGGATGGG | 286053 |
rs144307933 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144854 | TGTTGATCATATAAC[C/T]TTAATGCCTATTCAA | 286053 |
rs144326960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221297 | GTCACCCATGCTGAA[A/G]TGCAGTGACGCAATC | 286053 |
rs144365373 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089866 | TGTTCGGCAATAGTA[A/G]AACAAATATTATGGG | 286053 |
rs144373365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205688 | TTGTTTACCATTAAC[C/T]TAGTAATCACCTCGG | 286053 |
rs144375136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108637 | TAATTCAATAGCTAT[C/T]ATATATGACAACCAG | 286053 |
rs144409634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325075 | ACATTATCAAATTAT[A/G]TACTTTATATGCATA | 286053 |
rs144411786 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138982 | CTATGCAGAAGTTAT[A/G]TGGTGTAAATAAGTT | 286053 |
rs144430416 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155400 | TAATCAATCCAAAGA[A/C]TTATTGTGAAAATTA | 286053 |
rs144439742 | in-del | -/CTTTTACCAAAAAA | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234946 | CATTTCAAGTCCTGG[-/CTTTTACCAAAAAA]CTTTTCCCTGGCCAG | 286053 |
rs144477177 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200730 | GGCCTGCCTAGCTAC[A/G]TTGGGGAAGTTCTCC | 286053 |
rs144484193 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275557 | TTGTATTTCCTCGTT[G/T]GCTGCCCAGCCCAGC | 286053 |
rs144498079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106816 | GCCTGGCTAACATGA[C/T]GAAAACCTGTCTCTA | 286053 |
rs144499235 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276826 | GTGGAAGAGCTTCCT[A/G]TTTTTCACTGACCTG | 286053 |
rs144514656 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317716 | GAAACTAGGGTATTT[C/T]ACTTGTTAATTATGC | 286053 |
rs144550405 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250157 | ACCATGCCTGGCTAA[G/T]TTTTGTATTTTTAGT | 286053 |
rs144558883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347953 | TGTTTAGAAAATGTA[C/T]GCTGAAAGATCTTCC | 286053 |
rs144561460 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351286 | GGACTGTATTTGTAG[A/G]CCTTTGGAAATACTA | 286053 |
rs144583280 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286608 | ATGAGCCACTGCGCC[C/T]GGCCCAAATAACATC | 286053 |
rs144592398 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123357 | TACTAAGTTCCACAA[C/T]ATTTACTAAGCACCT | 286053 |
rs144637320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210868 | TAGGACTACAGGTAT[A/G]TGCCAATATGCCACT | 286053 |
rs144650435 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251585 | CAAAACCTGACATTG[A/G]CTTTTCCAAGTTTCC | 286053 |
rs144653490 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282858 | CCCTACTGGGCAGTT[C/T]TGGACTCCACTTGAA | 286053 |
rs144656323 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111105 | TTGTGTTCTGGCTAA[A/G]AATCATCACCTTTTT | 286053 |
rs144667444 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226493 | CACTGTACCCCTCAT[A/G]TCTGCAGCCGGGATC | 286053 |
rs144691028 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259563 | AAATTGTCTTCCATG[-/A]AACCGGCCCCTGGCA | 286053 |
rs144715915 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289334 | TCTCTTCTGCCTCCC[A/G]TCTTTGCGTTTGAAC | 286053 |
rs144715972 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246428 | ACCTTGTGATCCACC[C/T]GCCTCCTCCTCCCAA | 286053 |
rs144716020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168971 | GCATTTTTGTGTAGA[G/T]GAGGAAGCTAGGGCT | 286053 |
rs144751458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099885 | GTTTTTGAGATGGGA[A/G]AAGTAATGGTGTATT | 286053 |
rs144753535 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289501 | GTGTCTAGCAGGGTA[C/G]TTATCAGAGGGCATT | 286053 |
rs144820305 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168097 | AATCACTAATCGATG[A/G]GTTTAATTTCTATGA | 286053 |
rs144828320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245695 | ACAATAAAATGATCA[A/G]TCTAAGAGCTGGATT | 286053 |
rs144856800 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096046 | ATGCATGGAGCCTGA[C/T]AGGTGAGTAGTTTTC | 286053 |
rs144862117 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284532 | TAAGATACTTAGACT[C/T]AGCTGTATTCAGGAT | 286053 |
rs144868184 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301222 | TGGGAAAGGGGGCCT[A/G]AGGAAAATCACCTGC | 286053 |
rs144881075 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174984 | GTCATCATTAGTATG[A/T]GTGATTTTTAAATAG | 286053 |
rs144897558 | in-del | -/AC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118394 | AAAACAAACAAACAA[-/AC]ACACACACACACAGA | 286053 |
rs144909437 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250031 | TTTCGCTCTTGTTGC[C/T]CAGGCTGGAGTGCAA | 286053 |
rs144912802 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127340 | GGAGTACATGATAGT[A/G]AGGGCCATGTGTGTT | 286053 |
rs144919737 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171391 | ACTTAGCGATATAAC[A/G]GACCTGCTAATGCAG | 286053 |
rs144950102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307129 | GTTTCCTTTTCCTCT[C/T]TTTTAACATTGTGGG | 286053 |
rs144950173 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189420 | GAAGGAGAGGAAGTT[A/G]CTTATGAAAGGTTTA | 286053 |
rs144961916 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234684 | TCTTTCCCATCAAAC[C/T]AGTTATAAACTCTTA | 286053 |
rs144971871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103425 | TTTTTATTGGCATAG[A/G]TTTTGAGCAATTTGT | 286053 |
rs145001090 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145828 | TGGAGCTGCTTTCAT[C/T]TCTGTTGCTGCCGGT | 286053 |
rs145011022 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248305 | ATAAAGACAAAAGCA[A/G]TTGCTTCAAACTTGC | 286053 |
rs145035086 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231628 | GTGGATTAGAAAACA[C/G]CAGTGTGTATCATGC | 286053 |
rs145039878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193924 | GTATGTCGTTGATTT[A/G]TTTGCCAGGTCCTTG | 286053 |
rs145041755 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141696 | ATTTTAACTCTAATG[C/T]AGTCTCTGTGGAGAG | 286053 |
rs145042151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351368 | TAAAAAAAAAAAAAC[A/C]TATTCGAGTTACCTA | 286053 |
rs145043599 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303591 | CCCCTCTCGCTGTTT[A/G]GGAAAAGGAGGTAAT | 286053 |
rs145053094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135946 | TCTACAGAGAAGTCG[A/G]CCAAGGTTTTGATTG | 286053 |
rs145057388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267318 | AGCCAAGGGTACCTT[C/T]TCTAAATATATGTTC | 286053 |
rs145066634 | in-del | -/C | 0.0228947 | 0.104514 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133622 | GCTCGCACCTGTAAT[-/C]CCCCCCAGCTACTCT | 286053 |
rs145078267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347176 | TAGTATCTCCATTTC[A/G]TAGCTGAGAAGATTG | 286053 |
rs145094165 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184049 | GCTAATGAATTTCAG[G/T]TTTGGTGTTGGTCTA | 286053 |
rs145123639 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264806 | TCATTAACTCTTCCA[A/G]CTCTTTATAAAATAA | 286053 |
rs145125475 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310566 | TGTTTCTCATAACTA[C/T]ATTTAAATTCCCGGT | 286053 |
rs145129992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189225 | ACACAGATGGAATAA[C/T]GACAAGAGCACACCT | 286053 |
rs145132993 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260918 | CATGAGCCATCATGC[C/T]TGGCCAAATTTCTTA | 286053 |
rs145136317 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194907 | TTTCATATAATGTTC[A/G]TGTTTGTCTATTAGC | 286053 |
rs145137798 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305214 | ATACCTGGCATTAAG[C/G]TAAGGAATTTAATAC | 286053 |
rs145157809 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109234 | GGCAAATTCTCTACC[C/T]TCCAATTTGCCTCAG | 286053 |
rs145179145 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105232 | TACGGCTAACAGCAG[G/T]TGTCACTCATAATCT | 286053 |
rs145179959 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113881 | AGTGAGGTTTAGCAG[A/G]TTCTAGGATTGGGTA | 286053 |
rs145183453 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191362 | TCTTGAAAACACTTT[G/T]GTGTGTTTTTTCTTT | 286053 |
rs145187531 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198594 | ATTCGATTTGCCAGT[A/G]TTTTACTGAGGATTT | 286053 |
rs145201986 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316483 | AGCTGGAATTTTCAG[A/G]GCAGGCTCCAGACTT | 286053 |
rs145204645 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326233 | CTGCACTCCAGCCTG[A/G]GCAAAAGAGTGAGAC | 286053 |
rs145206342 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243350 | AGACTTATGTGTCAT[A/G]TCGAGAAATTTGGAT | 286053 |
rs145211230 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254277 | TATTTAATGGCTGGA[C/T]GCATGTCAGTGCATA | 286053 |
rs145226386 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128612 | AAGCCTGAAGTGAAT[C/G]TTAACTGGGCTAAAA | 286053 |
rs145269467 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362897 | TCAGACATTCTCAGC[A/G]TGCTCTCATGCACTG | 286053 |
rs145276147 | in-del | -/AC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123608 | CGCACACGCACACAA[-/AC]ACACACACACAAGTG | 286053 |
rs145295443 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268181 | CGAGGCTGCGGTGAA[A/C]CATGATCACACCACT | 286053 |
rs145324822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323520 | CCAATTAATTTTCTA[A/C]TCACATGCAAAGACA | 286053 |
rs145330270 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250261 | TCCCAAAGCCACCAC[A/G/T]CCCAGCAACACTATT | 286053 |
rs145337065 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194351 | AGAATTGTACAGTGT[A/G]TAGCCTTTTGAGTGG | 286053 |
rs145360043 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212435 | GGCAGTGAGAGCCCG[G/T]TATGTGCAGGAGGCT | 286053 |
rs145360508 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311285 | AGACACCAAAGAATT[C/G]CCTTTCACTCAGTTC | 286053 |
rs145372723 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285542 | TCTAATAGGGTTTTG[A/T]AGACTGACATAACAG | 286053 |
rs145397883 | snp | A/G/T | 0.0205699 | 0.0994467 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206930 | GCAAGGAGTGCTGCA[A/G/T]TGAGGGGAGAAGGAC | 286053 |
rs145436600 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328465 | CCTGGATTGGGTTGT[A/G]TGCCAGGCACAAGGA | 286053 |
rs145437789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264564 | TGCGCGCACCACCAC[A/G]CCCTGCTAATTTTTG | 286053 |
rs145438447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280921 | TCAAATGCATACTTG[A/C]CTCCCTGCCTGCTGC | 286053 |
rs145498097 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330620 | AAAATAAGCTCGCAC[C/T]TGGGCAACTCCAGAT | 286053 |
rs145511126 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213390 | ATATTGCTCATATGC[C/T]TAAGCTTCTTTGTTA | 286053 |
rs145514276 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249981 | TTTTATTATTTATTT[A/G]TTTACTTATTCATTT | 286053 |
rs145517916 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341462 | GCTAGGAGTCAGGCC[C/T]GTAGGCTTTGAAAAT | 286053 |
rs145549835 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295806 | AGCTGGATTTCTTTC[-/T]TTGTTTTTTAAGCTC | 286053 |
rs145558272 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129584 | TGTGTGTGTGTCTGT[A/G]TGTTTCATTGATATT | 286053 |
rs145572103 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282308 | TAGTAGAGCCGGGGT[C/T]TCACCATGTTGGCCA | 286053 |
rs145579379 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208550 | CTTTTAGTGGAAATA[A/G]ATATTTAAAATAGTT | 286053 |
rs145596983 | snp | A/G | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093036 | ATCCTTCTTGGTTGA[A/G]AACCACTTAAACCAA | 286053 |
rs145597089 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125595 | TAGAACTTCTGTACT[A/G]GAAATGAGGACATTA | 286053 |
rs145603034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209121 | CCAATTTGATTTTCT[A/G]TCGTCAGCTATTTGT | 286053 |
rs145669102 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191799 | CATACATCATCTCGC[A/G]TAATCTTTACAACAT | 286053 |
rs145676428 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141258 | AATTTATTTAAGTCA[A/G]TCAGTCTCTCTTTCA | 286053 |
rs145689589 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168234 | AACACTGTTCTTTGT[A/G]TAAATGCTGAGATGT | 286053 |
rs145702350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157968 | CTTAAAGACTCCAAA[A/G]CCTTTAATGTGCTTT | 286053 |
rs145704600 | in-del | -/T | 0.16028 | 0.233346 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240714 | TGTGTGTAATGGTTA[-/T]TTTTTTTTTTGTTAG | 286053 |
rs145712796 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356573 | ACCTCGTGATCCGCC[C/T]ACCTCAGCCTCCCAA | 286053 |
rs145741698 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307849 | CAGACACCAGCACTG[G/T]GAGCTGGATCTCACC | 286053 |
rs145744342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173820 | AGTAAAACATTTAAG[A/G]TGAACGGGGGTTTGA | 286053 |
rs145791409 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233487 | GTTTTTTATTTTTAA[C/T]AAGGTATTAGTACTA | 286053 |
rs145801621 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117366 | TGCTAGGATTACAGG[C/T]GTGAGCCACTGCTCC | 286053 |
rs145807634 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335598 | AGGAGCAAAATGGGG[A/G]TGATACTCCATGCAG | 286053 |
rs145808551 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104232 | CAACCTCAGGTAATC[C/T]GCCTGCCTTGGCCTT | 286053 |
rs145809100 | in-del | -/TA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217358 | ATTTATTTATTTATT[-/TA]TTTTTTATTTATTTA | 286053 |
rs145813037 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305338 | GTCATATAGCTAGCT[A/G]GTCAGTGTCTCCCTA | 286053 |
rs145818324 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350743 | TGGGAAAGATCTGCC[C/T]CCATGATTCAGTTGC | 286053 |
rs145862223 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093995 | TTTTTGTAGAGTTGG[G/T]GTCTTGCTGTGTTGC | 286053 |
rs145892764 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233606 | TTTCCGAAATGAAAT[G/T]AATGTAAATGCACTT | 286053 |
rs145893468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098802 | AGGTTTGGGGGAGGG[A/G]TAGGGTGGGAGAGAA | 286053 |
rs145894824 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152440 | GACACTAGTATTTTT[C/T]AGAAACTCATTCTAA | 286053 |
rs145902616 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224393 | CAGCCCAATGTCGTG[A/G]AGCTATTCCTAGTTT | 286053 |
rs145919110 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281980 | TAACTCCTGCAGGGG[C/T]CAGGGAGGGAAGGAA | 286053 |
rs145919127 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240060 | CTGAAAAGACAACTA[C/G]ATTATAGAACAGAAT | 286053 |
rs145946283 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166209 | AATGTTACGATCTCA[A/T]AATAGATGTTTTTGC | 286053 |
rs145953938 | snp | C/T | 0.000153988 | 0.00877328 | missense | NSMCE2 | GRCh38.p7 | 8:125366832 | ATCCAGGATGAAGCA[C/T]TTAGAAGGGCAATTG | 286053 |
rs145957293 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160790 | AAGACTGAGGAAATT[C/G]AGCCCTAAAATGTAT | 286053 |
rs145983768 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204514 | TCCATCTTTCCTTTA[C/T]ATGGAAGCATTAATT | 286053 |
rs145986071 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294791 | TATGAATTCATTCAC[A/T]GTGTTCCGAGGCCTT | 286053 |
rs145993580 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159193 | TGTTATCATTATTCT[A/G]TTTTTCTATCAGTTA | 286053 |
rs145995661 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222684 | TTCATCCATGTTGTT[A/G]CAAATGACAGAATTT | 286053 |
rs145998588 | snp | A/G | 0.000321791 | 0.0126804 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357829 | GCCTAGTGAGTGGAC[A/G]CAGGGAAGGAAGTGG | 286053 |
rs146004406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338770 | TGGGTTATAAATGAA[A/G]TTTATTCTAGGAGTA | 286053 |
rs146053168 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186531 | AAAAAGCAGGAATCT[G/T]TACATGCAGAAGACA | 286053 |
rs146065618 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099040 | TCATTCCTTCTTTCA[A/G]CAAGCCTTTGTTGAA | 286053 |
rs146080084 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181598 | GAACAGAACCAGGGG[A/G/T]CACTTATTCCTTGGC | 286053 |
rs146103919 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298651 | GAACGTGACCAGTGG[A/T]TCTTAACAGGGATTG | 286053 |
rs146107076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227536 | TGTCTAAGCTATAGC[A/G]TTAACTCCCAGTTTT | 286053 |
rs146107495 | snp | A/T | 0.0513262 | 0.151752 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366298 | GTAATCCCAGCACTT[A/T]GGGAGGCCGAGGCGG | 286053 |
rs146110104 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242220 | GGATTGAACCTGGCA[A/G]ACCCATGGAGAGAAA | 286053 |
rs146116767 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278184 | TTACATTATTATTTT[A/G]TTTTGTTTTCTTTTA | 286053 |
rs146117008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162707 | TCCTGTTAACTTTTT[A/G]CTTCTTTCTCTTACC | 286053 |
rs146130764 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280219 | AGAAGAGTTACAACT[C/T]CCTCTTCCCTGCCTT | 286053 |
rs146176361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204025 | GACAGATGCTTGTCT[G/T]TCTTAATCTGTTATA | 286053 |
rs146188671 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120009 | AAAAGTAAGAAGAAA[A/G]AGGAAAGATTACTTT | 286053 |
rs146199521 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116674 | AATTCCTTAACCTAC[G/T]TATGTCATTAGCAGT | 286053 |
rs146231031 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259945 | AAACTGCATTGGGCT[C/T]ATGTAATCCAACCTC | 286053 |
rs146231040 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303884 | ACATTGTTTGTATAA[C/T]GTGTCCCTAAGATGC | 286053 |
rs146237502 | snp | C/T | 0.0152352 | 0.0859388 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182283 | TGCTTTGCTTTGGTT[C/T]GGCTTTTTGAAATTA | 286053 |
rs146249309 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300551 | TGGTATCTCAGTAAG[C/T]TGGCACTGTTCCATT | 286053 |
rs146309212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144404 | AAAGAATCTTCTGCT[C/T]TCCTATCTGCTGTTG | 286053 |
rs146317617 | in-del | -/ACAGCCTGGA | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150882 | CATGTAAGTAAGGGC[-/ACAGCCTGGA]ACTCCTTAATACAAG | 286053 |
rs146319306 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139367 | ATCTTTGTTTAGCAT[C/T]ACTCTTTTTTTGTTT | 286053 |
rs146345765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186951 | AGGCATTAGATATAA[C/G]ATCTTTGAACAAAGA | 286053 |
rs146346018 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263842 | TCTCAAATATCAGCT[C/T]TAGCGTGTAAAGAGA | 286053 |
rs146350187 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276547 | AGCCTCATTTGAGTA[C/T]AAACTTCATAAAGGC | 286053 |
rs146370745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318706 | TCTGTGAAACAACCA[C/T]GGCACTCAAGGCATT | 286053 |
rs146378542 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250138 | GGTACTACAGTCATG[C/T]ACCACCATGCCTGGC | 286053 |
rs146408672 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257144 | CAAAAATTAGTCAGG[C/T]GTGGTGGCACGTGCC | 286053 |
rs146420761 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330207 | TTTTTGAGACAGTCT[C/T]TCTCTGTCACCCAGG | 286053 |
rs146435536 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102400 | GGTGTAGAGTCTGCT[C/G]TCTCCTCCTTGAAAA | 286053 |
rs146517413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130572 | TCTTTTTGATTGGAA[A/G]GTGGTATTGAGAAAC | 286053 |
rs146525429 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333922 | AAGATCAGTGGCATG[C/G]TGAACTCATGAATGG | 286053 |
rs146532859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272309 | TTGAGCCACCGCGCC[C/T]GGCAAATCTGCAGTT | 286053 |
rs146537233 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114177 | TTACCCCTTTCTCTG[C/G]TTTATTTTTCTCTCG | 286053 |
rs146544714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351297 | GTAGACCTTTGGAAA[C/T]ACTACTTCAAACATA | 286053 |
rs146551675 | in-del | -/TCAAAGT | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135586 | GGTACGAGGTATAGA[-/TCAAAGT]TCAGTATTTTCCTTC | 286053 |
rs146566560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243409 | ATGTTCCAAAAGGAA[G/T]ATCCAAAAGGATCTG | 286053 |
rs146592297 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177455 | CTTTGCCATCAAACT[A/G]TATTCATTGGTTCAC | 286053 |
rs146601791 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108716 | TGAAGAGGGTAAGAA[A/G]GATGGATGAGTTTGG | 286053 |
rs146614003 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238398 | ATCTATGAATATAAC[A/G]GAACTGAAACCATAT | 286053 |
rs146621432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164621 | TACTGTTATATGTAA[C/T]GGTTATATTAAAAAT | 286053 |
rs146625688 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156949 | GCAGGTTGGAAGTTA[A/C]CATTTTAGTTAAACC | 286053 |
rs146636800 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250182 | TTTAGTAGAGATGGG[A/G]TTTCACCATGTTGGC | 286053 |
rs146637079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152481 | AGGGTGAAAACCACT[A/G]ACTTAAAAGAACAAG | 286053 |
rs146644387 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355358 | GAGAAGGGAAAGGGA[A/C]AGGAGAAGGAAGGAG | 286053 |
rs146646374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277016 | CTGATGGCGCATGAG[A/G]TCTTTCTTACAGCAG | 286053 |
rs146665120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290850 | TAATGTAGTAGCACT[A/G]TCTCAGTATAAATTA | 286053 |
rs146704027 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302567 | TAACTACTGCTGATT[A/G]TTGAGCTTATAGAAG | 286053 |
rs146707086 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257955 | AGAGGGTGGTGGTGG[A/T]GGTTTTGGAGAGATG | 286053 |
rs146707755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111793 | CAGTAGAGTGAGACC[A/G]TGTCTCAAAGAAAAA | 286053 |
rs146720888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129175 | CTTAGGTGGGGAGGG[A/C]ATACGTGAAATGACA | 286053 |
rs146732810 | snp | A/G | 0.168785 | 0.236441 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256215 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 286053 |
rs146746800 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178678 | GATCGAGACCATCCT[A/G]GCTAACACGGTGAAA | 286053 |
rs146758227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175540 | TGGGAGGCAGACATC[C/T]AACAATGGCTGTTTT | 286053 |
rs146764698 | in-del | -/CTTTC | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116076 | ATTTATCTGTAGTCT[-/CTTTC]CTTTCTTTCCTCTTT | 286053 |
rs146766729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253751 | AAGTCGTATAGGCAG[C/G]CTGATTTAAAAGATA | 286053 |
rs146766786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295264 | AATCTGGTGACCTTT[A/G]TGTTTCTGTCAAAGA | 286053 |
rs146785935 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312129 | AATGATAAGGTCACA[A/G]AAAGAATAATAAAAA | 286053 |
rs146807493 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351571 | CATCGTCTATGTATA[A/T]AGAAAATAATATGAC | 286053 |
rs146818088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180000 | TTACCATTAACATCT[C/T]AGGTGGATGTGAGTC | 286053 |
rs146830856 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135546 | TCTGTGATTCTTTCT[A/G]ACTGAAGTTTTGTAT | 286053 |
rs146841844 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152058 | AGTGATTACTCAGTA[C/G]AAGATACATTTTTAA | 286053 |
rs146881009 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195320 | CCTGGCAATGCTAAT[A/G]TACAATGAGGGTTGA | 286053 |
rs146888311 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269068 | AATGGATTAAGATAT[A/T]TTTGACTCTTTAACT | 286053 |
rs146888514 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316357 | GCCTTCTTGGGAAAA[C/T]AGAACTTCCAGAAAA | 286053 |
rs146899455 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298066 | AGAAGTTCAAGACCA[C/G]CCTGGCCAACATGGT | 286053 |
rs146918953 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358359 | AAGGTTTAGGTAAAT[G/T]CATGGCTAACTCATG | 286053 |
rs146957204 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137127 | ATAGAAATTATTCTC[C/T]GACAGATAGGAATAT | 286053 |
rs146958911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261966 | GCCAGGTGTGGTGGC[A/G]CACACCTGTCATCTC | 286053 |
rs146966460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185520 | CATGTTGGCCAGGCC[A/G]GTCTTGAACTCCTGA | 286053 |
rs146974720 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273687 | CGATTCACTGGATTA[G/T]CATCTGAATTTCTCT | 286053 |
rs147020856 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314353 | GGAGTCCAGTGGCAC[A/G]ATCTCAGGTCACTAC | 286053 |
rs147049615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158368 | AAGACCCCTCTGTGC[A/G]GTGATGATATGAGAA | 286053 |
rs147063407 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277716 | CGACGGGGTTTCACT[C/G]TGTTAGCCAGGATGG | 286053 |
rs147071842 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154130 | AATTGCGATACTTCC[A/G]TTACTATAATATTTG | 286053 |
rs147072168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202122 | AGGTACAGTCTGTCA[C/T]GGCTTCCCTTGGCTA | 286053 |
rs147081342 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265349 | ACCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG | 286053 |
rs147082286 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218524 | TCAAGCAATTCTCAT[A/G]CCTCAGCCTCCCGAG | 286053 |
rs147092454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138262 | CTGGTCAATCTCTGT[C/T]ACTCAGGATGGAGTG | 286053 |
rs147110451 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262161 | CCGGGTGCGATGGCT[C/G]ACACCTGTAATCCCA | 286053 |
rs147124314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331982 | AAAGCTGCTTTGTGG[A/G]CTTAATCTATTTAAT | 286053 |
rs147127861 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348770 | AGGCCTCTCCAGCCA[C/T]GTGGAACTGTGAGTC | 286053 |
rs147187372 | in-del | -/GTTTTTTTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186388 | CAGAAGTAACGGCAG[-/GTTTTTTTT]TTTTTATTTTTTTAA | 286053 |
rs147198314 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106722 | TCATTTTGGCCGGGT[A/G]CTGTGGCTCACACTT | 286053 |
rs147206566 | in-del | -/AAAC | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214047 | GAAGCAGTTTACATT[-/AAAC]AAATAACTTTTATTT | 286053 |
rs147207689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154894 | CTCCCTTGCTTTCTA[C/T]GCTTTTATTAAGTAC | 286053 |
rs147207955 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101451 | GAGATTCAGAGATGT[G/T]TAGCAGTCTTCATGT | 286053 |
rs147214768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237438 | ACTGTCAGATCAACA[A/G]CACCTGCCAGATTGA | 286053 |
rs147230859 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149820 | TAGTGGCTTGTTTTC[A/T]TGTGTATTATAGGTA | 286053 |
rs147231054 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274057 | ATTCACCTAAATGAT[C/G]ATGTCATCCTCAGAG | 286053 |
rs147233876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288721 | AACACTCGAGATACT[A/G]TGTACCTGTGTTCCC | 286053 |
rs147251238 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285646 | TATCAATAAATAACA[C/G]CAACATGTGAAGACA | 286053 |
rs147280993 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328638 | TCCACATGATTCACA[A/G]GCTGGTGCACAAATT | 286053 |
rs147281549 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111156 | TACCTTAATCCCCAC[A/G]CAGCCAAAAAAGTTT | 286053 |
rs147304478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127325 | TGTGCTGAGGTTGGG[A/G]GAGTACATGATAGTA | 286053 |
rs147312857 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297233 | ATTCCTATAAAAATG[-/C]CTGGCCAAAAGGTAG | 286053 |
rs147314440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122257 | GAAGATACTTCAACA[A/G]ATCTCTAGATCCTTA | 286053 |
rs147321147 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255062 | GCGTCCACTTCCTGT[A/C]TCCTTGTATGCTCAC | 286053 |
rs147337686 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292936 | ATACTTGTTGAAGAC[C/T]CCCTGTAGTCTGGAG | 286053 |
rs147337918 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251324 | CACAAATGAACTGGA[A/G]AAAAAAGTATTTTCA | 286053 |
rs147338055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173289 | ACCAGAGTCGCAGTG[A/G]TGGGGGAATTGCAAG | 286053 |
rs147339347 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250118 | CCTCAGCCTCCCAAG[C/T]AGCTGGTACTACAGT | 286053 |
rs147340717 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309977 | TCAAGATCATGAAAC[A/T]TGTAAGCTGGCAGGC | 286053 |
rs147356949 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304792 | CTGATTCTCATCAAG[C/T]GATGAGAATCGCTTG | 286053 |
rs147386133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349973 | GTGTTTGTGTTGCCA[C/T]GTCTGCTAAATATGT | 286053 |
rs147431523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240440 | CAGCTTTCAGAATTA[C/T]ATTACTGTCTTCAGA | 286053 |
rs147441025 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106871 | CGTGGTGGTGGGCGC[A/C]TATAATCCCGGCTAC | 286053 |
rs147443718 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193377 | AATAAGAGACAACAC[A/G]CTTCTGTTTAAAAAT | 286053 |
rs147445535 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328017 | ATGGGTGAGGTTTTC[C/T]AGCACAAGGAAAATC | 286053 |
rs147462067 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325932 | ACTCCAGCCTGGGCA[A/C]CAAGAGTGAAACTCC | 286053 |
rs147518526 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295372 | GCATCCAAAAGGGCC[-/A]TTTGATAATAAAATT | 286053 |
rs147524214 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133845 | CTCAGAGAAAACGCC[A/G]TTTATGATTTTTAAC | 286053 |
rs147526863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215856 | GTACAATATTTGTGC[A/G]TTTATCACTTGAACC | 286053 |
rs147536498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212367 | GCCATTCTGGGGTAA[C/T]AGGGGAAGCTCAGGG | 286053 |
rs147539650 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250045 | CCCAGGCTGGAGTGC[A/G]ATGGCGCAATCTCGG | 286053 |
rs147545146 | in-del | -/CCA | 0.0759472 | 0.179459 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278772 | AGCTGAAATTCACTT[-/CCA]CCACCTGTTCAAAAA | 286053 |
rs147547406 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127429 | AAGAAACAAAAGTAT[A/G]TTCTAGTTTTAGAAA | 286053 |
rs147548810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258316 | GAAAATGGAAACAAG[A/G]GCTAGCTCACAAGAG | 286053 |
rs147557005 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093701 | GCACTCCAGTTTGGG[C/T]GACAGAGCGAAACTC | 286053 |
rs147557207 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146097 | TAGCCTCTGAGTGGC[A/G]TTGTCTAGTGTCCTC | 286053 |
rs147559661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228991 | TGAGGTAAGATGATA[A/G]CCTTGAAAACTGTTA | 286053 |
rs147568476 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267405 | ATTTTTATGTGAGAA[A/G]TAAGGCTAGACAGTG | 286053 |
rs147580361 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142116 | GTATTTAGACTAATT[A/G]CACTTGCAGAATAGT | 286053 |
rs147597821 | in-del | -/T | 0.0832709 | 0.186283 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183402 | CATATTTTAAGTTTA[-/T]TTTTTGTTCTTTTTT | 286053 |
rs147598286 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264870 | CCTTGACACATGCAA[A/C]TATCTCATTTAATCT | 286053 |
rs147617962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322410 | CAGAAAAAGCATTTG[A/G]CAAAATCCAATACTG | 286053 |
rs147663277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168420 | GGACATTTGTCTTGG[C/T]TCATTTGGCCTACTG | 286053 |
rs147685565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163731 | TTCCTGATTCTACCA[A/G]CAAGAATGGGAAGGG | 286053 |
rs147685848 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212734 | TTTAAATGTAGGATA[C/G]GATCAGTTCACTGTA | 286053 |
rs147695573 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207768 | GGCTGGGAGCTTCTG[C/T]GCCTAGAATGTCTTC | 286053 |
rs147702129 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281012 | GGAAGAAAACTCTGC[C/G]TGCCTATCCAGAATG | 286053 |
rs147706625 | in-del | -/ATAAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262105 | TGTCTCAAAATAAAA[-/ATAAA]TAAAATAAAATAAAA | 286053 |
rs147718327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345879 | GGCCATGGTCAGCCA[A/G]GCATGGTGGTTCATG | 286053 |
rs147721894 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341463 | CTAGGAGTCAGGCCC[A/G]TAGGCTTTGAAAATG | 286053 |
rs147767774 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188789 | TTCATTTGGGAATGT[A/G]TATTGTAGAAACCTG | 286053 |
rs147788194 | in-del | -/TG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326476 | TTTGTGTATATACAC[-/TG]TGTGTATGTGAGGGA | 286053 |
rs147788750 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097855 | TGAAAAGCGTGTTTG[C/T]ATTATATTGTAGAAA | 286053 |
rs147790719 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185131 | TGCTAGGAATCTTTT[A/C]GGTGGGGAGAGGCCA | 286053 |
rs147791903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233061 | AGGGATGTGACCTTA[C/T]GGAAAAGTAAGGAAT | 286053 |
rs147800368 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229974 | AATTTTCAAGATCTG[G/T]AAATATTTAGTTGAG | 286053 |
rs147805726 | in-del | -/C | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357492 | TGGAGAGAGCTGTCA[-/C]GTCAATCATGCCCTG | 286053 |
rs147806343 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301820 | GGCACCAACCAACCA[C/T]GCCCGGCTAATTTTT | 286053 |
rs147825305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363525 | GAGGAAAGAGGAGAG[A/G]AAGAAAGAAAGAAAG | 286053 |
rs147871506 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123620 | CAAACACACACACAC[A/G]AGTGTGCATCTTGTG | 286053 |
rs147873255 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206728 | TCATTAATGTCAAGC[A/G/T]TACTGAATTTAAGGT | 286053 |
rs147875429 | snp | C/G | 3.29462e-05 | 0.00405857 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102444 | TATCAACTCTGGTAT[C/G]GACACAGCTTCTAGT | 286053 |
rs147893842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117756 | GGTCTTCCCTTTTAA[C/G]TAGGTTTCCTGAGGA | 286053 |
rs147896719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201809 | ACAGAGGTGGAGTCT[A/G]TAGAGGCAGTAGCCC | 286053 |
rs147911728 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320782 | GAAAATGATGCAGTA[A/T]TAGTTCTCATACTGC | 286053 |
rs147913679 | snp | C/T | 0.153997 | 0.230832 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246434 | TGATCCACCCGCCTC[C/T]TCCTCCCAAAGTGCT | 286053 |
rs147929778 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262153 | TGTATAGGCCGGGTG[C/T]GATGGCTCACACCTG | 286053 |
rs147977793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365104 | CTTTAGCTGCAGCCT[G/T]TCCACCGAGTCCCAG | 286053 |
rs147980001 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282742 | AGTAATAATGCTACA[C/T]AGCTTATCCCTTCAA | 286053 |
rs148011228 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172534 | TCCCCCTCCCCAAAA[C/G]GGGGAATGATACATC | 286053 |
rs148063308 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165774 | TTTTGATTAGACTTG[G/T]GATGGATAGAATTCA | 286053 |
rs148068720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244120 | ATAAATGATTCCTCA[A/G]AAAAGAATAATGTAA | 286053 |
rs148084963 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258656 | AAATAATAGGAAAGA[G/T]TAGAAGGGACTCAAG | 286053 |
rs148086874 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181372 | ATGTAATAAAGAACA[A/G]GGTTGAGAATGGATA | 286053 |
rs148088566 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298458 | TGAGATCCAGCGTTT[G/T]CAGTCAAGCAGATTG | 286053 |
rs148094571 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195695 | ACATTCTGGCACTGA[C/T]CATCAACCCACTTTA | 286053 |
rs148105806 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110723 | GTGCAGTCAAATGAC[A/G]TTTAGCGACGTTTTG | 286053 |
rs148122742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239964 | GCCCCTTCTTGCTCA[C/T]TGCTGAGGCCACTGT | 286053 |
rs148135096 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360270 | CAGCAAGTGTGAGTT[C/T]TGCAGTCAGGGGAGG | 286053 |
rs148137213 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143527 | ATGTTGAATTGGAGT[C/T]AGCAACCCCTTAAGA | 286053 |
rs148139014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254719 | TAATCCTCTTGCTAA[C/T]TGATGTGACTGAGTT | 286053 |
rs148147051 | snp | A/G | 0.130351 | 0.219509 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191055 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC | 286053 |
rs148190439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323218 | ATACTTAAGATGCCA[A/G]TTCTCACCGAATTGA | 286053 |
rs148210527 | in-del | -/TTAT | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119864 | ACTTTATAAATGAAA[-/TTAT]TTGTTATATATAAAT | 286053 |
rs148224891 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210889 | ATATGCCACTATGCC[C/T]GGCTAATTTTTTTTG | 286053 |
rs148247895 | in-del | -/TTA | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188651 | AATTTTTTTAGTGCC[-/TTA]TTAGGCACTTTAATG | 286053 |
rs148254050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159322 | AATATTTCAGTTAAC[A/G]AGGGGCCATACATAT | 286053 |
rs148265143 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309103 | TACAAAAAATTTAGT[A/T]GGGCATGGTGGCGCA | 286053 |
rs148276745 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203301 | TCCTGTCAACCTGTT[C/T]GCCAGATTATAGACT | 286053 |
rs148280252 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278271 | CACATTCCTGCGGAG[A/G]TATTGAGCAATCTTT | 286053 |
rs148286830 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218670 | ACCCGCCTCAGCCTT[C/G]CAAAGTGCTAGGATT | 286053 |
rs148299414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337660 | AGCATGTTGGGAAGC[C/T]GAGGCTGGCGGATCA | 286053 |
rs148301246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262747 | CTTTAGGTGAGACCC[A/G]TTCTGTGTTAGTTTC | 286053 |
rs148303574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234885 | CCCCACCCCATCCCC[C/T]GCCACCTCTGTCCTC | 286053 |
rs148318463 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153340 | ATAGGAAGAAAAAAC[A/G]TAGTTATTTTTCTTT | 286053 |
rs148332962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273537 | CTGCCTTCCTACAGC[A/G]TCCTAAATTTGATTT | 286053 |
rs148337980 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214435 | TTGGCAGGCAAGGAG[A/G]CTGAGTCATGGGGGC | 286053 |
rs148346171 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098589 | TGATGGTTTGAATCA[C/T]GGTGTTATCAGCAGA | 286053 |
rs148348730 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287405 | TACAAGCCCAGTGCC[A/G]TTGTTTCATGCCTGC | 286053 |
rs148352302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331704 | TGTTAGAAGTTATTT[A/C]ACTGCTTCAGAACCC | 286053 |
rs148404903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237842 | GCATCGTTTTGTGCC[A/G]TGTTTCCTTTCCATT | 286053 |
rs148408838 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213526 | TCTCCTCTCCTCTCC[A/T]CTCCTCTCCTCTCCC | 286053 |
rs148421189 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275797 | TCATGAGAGGCTAAG[G/T]TTCAGAATGATTAAG | 286053 |
rs148443056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187149 | ATGTGGCTTAGCAGA[C/T]GGAAGACTTGGATTT | 286053 |
rs148445933 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348720 | CCATGTAAGACGTCC[-/T]TTTTTTTCTTCCTTC | 286053 |
rs148450183 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289879 | CATTTATTATCAAAG[C/G]CTTTTTGTTTATGAG | 286053 |
rs148453308 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101170 | GATTTTTGAATGGGT[C/T]TCATGATTGACATGG | 286053 |
rs148466485 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333216 | GCTCTGTCGCCAAGG[C/T]TGAAATACAGTGGCA | 286053 |
rs148502122 | snp | C/T | 0.0543475 | 0.155628 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367385 | CCAGGTGTGGTGGTG[C/T]GCACCTGTAATCCTA | 286053 |
rs148503695 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285048 | TTCTAAATATAGTCT[A/G]AATTAGAGGCAAATG | 286053 |
rs148529205 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297316 | GCTTATTTTACCCAG[-/T]TTTTCCCCTCCCCTG | 286053 |
rs148539842 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173945 | ATAATGATATTTTTG[C/T]GTATATAAGGCTTTG | 286053 |
rs148568722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117378 | AGGCGTGAGCCACTG[A/C]TCCCAGCCTTCAGTC | 286053 |
rs148574366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350829 | GACACAGCCAAACCA[C/T]ATTAGGTTGTCAGGG | 286053 |
rs148578529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245889 | CAACTAACTAGGTGT[A/G]GTGAGGCACCTGTAA | 286053 |
rs148588332 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133902 | TCTCAAATTTTATCA[C/G]TAATCAGAATCACTT | 286053 |
rs148590752 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168162 | TTTAAGCTGCCTCTT[C/T]CTAAGAGCATAATGT | 286053 |
rs148621680 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197918 | TCACATCCCTTGCAA[A/G]TTGGATTCCTAGGTA | 286053 |
rs148623301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301512 | TGAACTTATTCACCG[A/G]AAGTACTTGGAAGAC | 286053 |
rs148629456 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314932 | GGAATGGGAGCAACT[A/C]ATTCCAGCAAGGGAG | 286053 |
rs148657901 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328906 | CACTGTTTCAGTGAG[A/G]CCCGAAGTCAGAACT | 286053 |
rs148660714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256012 | TAACTGGCCGGATGT[G/T]GTGGCTCACGCCTGT | 286053 |
rs148663799 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144856 | TTGATCATATAACTT[C/T]AATGCCTATTCAATA | 286053 |
rs148666242 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266698 | AGATCCAGTATACCT[C/G]TTGGGGATGAATAGC | 286053 |
rs148673434 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192866 | TAGATGATGATGACG[C/T]GCTCTACTGCTAACA | 286053 |
rs148677572 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250139 | GTACTACAGTCATGC[A/G]CCACCATGCCTGGCT | 286053 |
rs148710044 | in-del | -/TC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124471 | GGATTCCTCAGGATT[-/TC]TCTCTCTCTCTCTCT | 286053 |
rs148711548 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325882 | ACTTGAACCTGGGAG[C/G]CGGAGGTTGCAGTGA | 286053 |
rs148716217 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139061 | GTGTTCTAGGGAGGC[A/G]CTGAATCAGCTCTGT | 286053 |
rs148737726 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212813 | AGGCAGAGGGTGACT[A/G]GATTTCAGCCCGGGT | 286053 |
rs148780406 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162763 | TTAAATTGGTGAACT[A/C]CTCTAAACCACCTAA | 286053 |
rs148788185 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280499 | AAGCAATAAAGCTGA[C/G]TTGACTCTGGACTTT | 286053 |
rs148799393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090503 | ATACAGGCTATATTA[C/T]TATTGGCATGAAATC | 286053 |
rs148803582 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205923 | GTGCCAAAACTCTTT[A/C]ATATATTGTCCTGGT | 286053 |
rs148814239 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223461 | GGAGTGCAGAAATCT[C/G/T]TTTGACATACCAATT | 286053 |
rs148843134 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340430 | ACTGAATTAGCTCTG[-/A]AAAAATATGAGAAAC | 286053 |
rs148856087 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098420 | TCCCGGTGAGTCAGG[A/C]AGTCCTTAGGAGTTT | 286053 |
rs148891635 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282329 | ATGTTGGCCAGGCTC[A/G]TCTCGAACTCCTGAC | 286053 |
rs148896801 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178722 | AAAAATACAAAAAAT[C/T]AGCCGGGCATGGTGA | 286053 |
rs148898678 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209101 | ACAGCCATGCACCAC[G/T]GTGACCAATTTGATT | 286053 |
rs148902901 | in-del | -/AGAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313201 | GAAAGAAAGAGAGAG[-/AGAA]AGAAAGAAAGAAAAG | 286053 |
rs148907625 | snp | G/T | 0.0402882 | 0.136092 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093431 | CAGTGGCTTATGCCT[G/T]TAATCCCAGCACTTT | 286053 |
rs148908528 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326173 | GAAGCAGGAGAATGG[C/T]GTGAACCCGAGAGGC | 286053 |
rs148917118 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109797 | TACGTTAGAATATAT[G/T]GTGTCTAGGCAATTA | 286053 |
rs148936724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342533 | AAGGAAGGCTTAGAG[G/T]CAAGGACTTTGTTCT | 286053 |
rs148940031 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158054 | TAACTAGAACATCTC[C/T]CTGGAGGAGGGACTG | 286053 |
rs148941466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239534 | GAATTGCTTTAACCC[A/G]GGAGGCAGAGGTTGC | 286053 |
rs148968467 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103434 | GCATAGGTTTTGAGC[A/G]ATTTGTGATGTGCCG | 286053 |
rs148971345 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189464 | CCTGGGCCTGTCCAG[A/T]CATGCCTAAATAAGC | 286053 |
rs148981238 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233533 | ATGCAATAAATTGAA[A/T]ATATAGTAATTTTGT | 286053 |
rs148991640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305696 | CTAGTTTAGAAACTC[A/G]TATACCTGCATACTC | 286053 |
rs149005286 | in-del | -/GAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327287 | AAAAAAAAAAAAAAA[-/GAG]AGAGAAACCAAAATT | 286053 |
rs149022041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184590 | ATTTCAAATGACAGA[A/G]CAAGCAAAATATTAA | 286053 |
rs149048441 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254370 | TGAATTACAATGGTA[A/G]CTGTAAACGGGACCC | 286053 |
rs149086109 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202985 | AAGACAGAAACTGAA[A/G]TGTCAGGAATTGCTG | 286053 |
rs149099116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322813 | ATATACTAGCAACAA[A/T]CAGAATTTAAAAATT | 286053 |
rs149101716 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248690 | TCCTTGATACATTAA[G/T]TTTTTTCAGAGAAAG | 286053 |
rs149117071 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136061 | TCTTGTTCTTTCCTC[C/G]TTGCATGATGATGTC | 286053 |
rs149149723 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272730 | TAATATATATATATA[C/T]ACACACACACATATA | 286053 |
rs149169284 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128771 | ATGGCCCATTGAGTC[G/T]TTCTCATCCTGCATC | 286053 |
rs149174348 | in-del | -/AC | 0.0543475 | 0.155628 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366660 | TTGGTCCTGATTTTG[-/AC]ACTTTTCCTTTTTCA | 286053 |
rs149182550 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230173 | TTATCAAGCCTAAAC[A/G]TGTCTTCCAGACAAA | 286053 |
rs149204097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268422 | TTTATCATGGGCTGC[C/T]TAGAGAATGATCACT | 286053 |
rs149246955 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200299 | TTTGGCATGTTTTTG[C/T]GGTGGCTGGTACCAG | 286053 |
rs149251849 | in-del | -/AT | 0.0364509 | 0.129988 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234585 | ACCAGGGATTTTCAC[-/AT]GTTTTGTCTCATTCT | 286053 |
rs149253948 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275447 | CTGTACCCTCCCATG[C/G]TATCCAGCAGGTAAG | 286053 |
rs149265977 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132100 | ATATTCTTCTTCTTC[A/T]TATGGGGAGTTGGTG | 286053 |
rs149269868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317646 | GGTCAGCATAAGCCA[A/G]TGTGAACTCAGTATA | 286053 |
rs149278296 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113057 | TATATTAACAGAAAA[-/T]GGGGGGGGGGGTGAG | 286053 |
rs149289489 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148775 | AGGCTGGTGTGAAAC[C/T]AATAGTCTATTTTTC | 286053 |
rs149303341 | snp | A/T | 0.000153988 | 0.00877328 | missense | NSMCE2 | GRCh38.p7 | 8:125357713 | CTCCTTGATTACAGG[A/T]GGAAATGAAGAAGCC | 286053 |
rs149304598 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347780 | GGTGGATTGAGTTGC[A/G]TTGGGTTAGATTGGA | 286053 |
rs149307540 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270668 | GATGGGAGGATCGCT[G/T]GAGGCCGGCAATTCT | 286053 |
rs149310577 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324016 | GAAATGAACAACAAC[-/A]AAAAAAACTAACATG | 286053 |
rs149343296 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226417 | TTGTAACTGAAGCTA[A/G]TGCAAATGAGGACAG | 286053 |
rs149371509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099795 | ATACAAATCTACAGA[C/T]GAGTTTTGCTCTAAG | 286053 |
rs149379363 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332885 | CTTTGAGTTGTCCTG[A/T]ATGTGGTAAGCTACC | 286053 |
rs149424309 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095666 | TTGGGAGGCCGAGGC[C/T]GGTGGATCACTTGAG | 286053 |
rs149426902 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180731 | GAAACTGGGGGGAGG[A/G]GATCAAGATTAGATT | 286053 |
rs149430490 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284022 | AGCTGGGCGTGGTGG[C/T]GGGCGCCTGTAGTCT | 286053 |
rs149449134 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111574 | GGAGGCCGAGGCGGG[C/T]GGATCACTTGAGGTC | 286053 |
rs149470003 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125835 | GAGTATCATAGTTCA[C/T]CTTGTTGTCCCCTCT | 286053 |
rs149471234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279192 | AATATTTTGATAGAT[A/G]TGGTTCCGTGCACCT | 286053 |
rs149479283 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176719 | TTATTTACCTCACAG[A/C]GACACTATACATTGT | 286053 |
rs149481981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359668 | TCCTTATCCATAAAT[G/T]AATGACAATCGTTGT | 286053 |
rs149502633 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192085 | TGGGTGTTTCTCTCA[C/T]TGTGACTTATTTTAA | 286053 |
rs149512115 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213521 | TCTCCTCTCCTCTCC[C/T]CTCCTCTCCTCTCCT | 286053 |
rs149514102 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110759 | ATAATTTTGGTTGTT[G/T]TTGTTTTTTTTTTTT | 286053 |
rs149518621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308387 | ATTGGCAATTATCCT[C/T]GCCTAATGGTCTTCT | 286053 |
rs149521007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237050 | ATTCTTCTGTACCTG[G/T]CACAGCAGTGAACAT | 286053 |
rs149535698 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352126 | AATAATGTATATGAC[A/G]TGCTTAGCACTGTAG | 286053 |
rs149554179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186525 | AAAAGCAAAAAGCAG[G/T]AATCTGTACATGCAG | 286053 |
rs149571690 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303460 | TGAAGGAACTAAACT[A/G]TAAAATAAAAGGTCA | 286053 |
rs149591669 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294329 | TTATCTCACAGTGTA[A/G]TTGCTGGGTCATATG | 286053 |
rs149628016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251047 | CAGCTGTTAAAAGTA[A/G]TTGTCTTTGATGGTA | 286053 |
rs149638288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325062 | TGAACAGATGTGTAC[A/C]TTATCAAATTATATA | 286053 |
rs149646195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262517 | TTCATCCATTTATTA[A/G]TATTCATCCATTTAT | 286053 |
rs149661850 | in-del | -/AGA | 0.0505692 | 0.150756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136697 | GCTTATTCCCATTAT[-/AGA]AGTAGTTTACTTCAC | 286053 |
rs149695365 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267485 | AGGAGTTGAATGCTA[C/T]GCTAAGAAATCAGTA | 286053 |
rs149720820 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092692 | CATGGATTTAAAGGA[A/G]GTCAACATATTGTCT | 286053 |
rs149743476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141111 | TATTAATTGAATTCA[C/T]ATACTTTATTTCAAA | 286053 |
rs149747002 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339362 | CTAGAGTCCTTTGGA[C/T]TGGGGGCTCTGTCTT | 286053 |
rs149748865 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264313 | ATAACCCTCAACAGG[A/G]TGGAGAACATATGCC | 286053 |
rs149750643 | in-del | -/GGC | 0.187435 | 0.242045 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242106 | GTAAACAATAACTGG[-/GGC]GGGGGGAGTTTGAGA | 286053 |
rs149774690 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173547 | TGGTAAGAAGAGCAA[C/T]CCATTAGCATCATAC | 286053 |
rs149776538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201796 | CTATGCCCTGTCCAC[A/C]GAGGTGGAGTCTATA | 286053 |
rs149794458 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320375 | AAAACTGTGAACCCA[C/G]AGTTTTCAGATTTCA | 286053 |
rs149797600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216233 | TCAATGGACATTTGC[A/G]TTTTCACCTTTTGGA | 286053 |
rs149827041 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167677 | GGCAAAGAGGCTATG[A/G]AAGAAATTATGCTAA | 286053 |
rs149832095 | in-del | -/TTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299805 | ATAATTTTGGCTTTC[-/TTT]TTTTTTTTTTTTTTT | 286053 |
rs149901620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102623 | GTCTCATTTTATTCT[A/G]CACACCGCAGCAGGG | 286053 |
rs149908503 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233457 | GGATTTTTATTCCTT[A/C]AAGTCACATGTGGAG | 286053 |
rs149912018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151758 | TTTTTCCAGAAGCCA[A/G]ACTTATCTTTGTTGA | 286053 |
rs149927742 | in-del | -/AGG | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285262 | ATTATACCAGAGCTT[-/AGG]AGAATAAAAATAAGT | 286053 |
rs149949662 | in-del | -/GGGAAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320308 | GAAGGAAGGAAGGAA[-/GGGAAG]GGAAGGAAGGGAAGG | 286053 |
rs149953787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096934 | GAATCCTAAAGTGTG[C/T]GTGACTCCATTATAA | 286053 |
rs149956506 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182973 | CATACCAATTTTATA[C/T]AAATTGATTTTTTCA | 286053 |
rs149959702 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300959 | GTGGTCATCTCAGTT[C/G]CAAATAGTGTCCTGT | 286053 |
rs149965985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228830 | TTAGCTCATTGAATT[C/T]ACGTTACAATCCTGT | 286053 |
rs149975857 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316450 | ATGACACTACTGGCA[A/G]TACGTGCATTGGTCA | 286053 |
rs149990685 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243339 | AAGAGAGTTACAGAC[G/T]TATGTGTCATATCGA | 286053 |
rs150005488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362506 | ACTAGGGCAGGGACT[G/T]GTGCACGGCAGGACC | 286053 |
rs150007877 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177419 | TCTCATTCCCATGAT[C/G]TGCTTCTCATCTTGT | 286053 |
rs150009430 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255515 | GTTGGAGAATAAAGG[G/T]TGGCGTGTTCTAGGC | 286053 |
rs150015516 | in-del | -/T | 0.234401 | 0.249513 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275771 | ATACTAATATCCAGA[-/T]TTTTTTTTTGTCATG | 286053 |
rs150028775 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311026 | CCAACTGAAACCGAA[C/T]TGATTTTTATCAGAT | 286053 |
rs150035978 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122051 | CTGTGCTCAGTGTAG[A/C]TAGCTCTTTTGCAGA | 286053 |
rs150038539 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205190 | CTCAATGCAGAAATC[A/T]CTGACTTCAGGGAGT | 286053 |
rs150077580 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317189 | TAAAGTCAGTGGTTT[C/T]CTAAAGATCTTTTTT | 286053 |
rs150079475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244408 | CTTAACCTATATGGC[C/T]AAGGGAGGGGGAAAG | 286053 |
rs150101608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179661 | TTACAGCAGTTTTCT[A/G]AAAGTTCTGGTTATG | 286053 |
rs150114313 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297490 | TCTTCTTTAAGGCCT[A/G]CTTCTCCACATTAGC | 286053 |
rs150129107 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250130 | AAGTAGCTGGTACTA[C/T]AGTCATGCACCACCA | 286053 |
rs150130208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313036 | TGTGCAGCAAACCAC[C/T]ATGGCACATGTATAC | 286053 |
rs150146081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208191 | CTGCAAAACAAGGAG[A/G]TATTTGAAGTAATCT | 286053 |
rs150147787 | in-del | -/TTATA | 0.45843 | 0.138046 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089930 | TTCTATATATAAACT[-/TTATA]TTAAATTTTTAATGC | 286053 |
rs150164776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253190 | GGCAAATATGGAAGT[C/T]TATATACACTTAAGG | 286053 |
rs150168649 | snp | G/T | 0.00164513 | 0.0286332 | missense | NSMCE2 | GRCh38.p7 | 8:125182215 | AAAATAATGAAAAAT[G/T]TGTACAGTTTAAACA | 286053 |
rs150225277 | snp | C/T | 0.093777 | 0.195178 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196849 | CCTACTTCTCCACAT[C/T]CTCTCCAGCACCTGT | 286053 |
rs150225399 | in-del | -/TT | 0.0437281 | 0.141251 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213068 | TACCATTTAATTCTC[-/TT]TTATAAAATGAGAAT | 286053 |
rs150230269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196103 | CCAGGCTCCTGGTCT[C/T]GACCTCCTGACCTTA | 286053 |
rs150249235 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095071 | GCCTGGGCTGGTCTC[A/G]AACTCCTGGGCTCAA | 286053 |
rs150258277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144058 | AAAAGAGGGGGGGAA[A/T]GTCCTTATTTTCATG | 286053 |
rs150260615 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225498 | AGAGGTTGAAGAAGT[C/G]AAAATCATCAGCTCA | 286053 |
rs150271884 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265610 | CCCTCTTAAATTTTG[C/T]CTCTCAGGCAGGTGG | 286053 |
rs150279029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157801 | TTTTAATCAGACTTA[C/T]AAAACTGTTACTGGG | 286053 |
rs150282974 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342049 | GGGGAGACTCCTGGG[A/G]ACCCCTGAGTGAGAA | 286053 |
rs150287373 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278473 | GGTGCTGCCAGCAGA[G/T]CAGAGCGTGTGCTTT | 286053 |
rs150302512 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176285 | AAAAATCTAATGCAC[A/G]CTTTTCACTTCTTAT | 286053 |
rs150319807 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291221 | CTTTGCTTATTCATC[C/T]GAAGAGACTGGAGGT | 286053 |
rs150336571 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335381 | GGTGTTTCCCCTGTG[C/T]GTATGACAAAACGCA | 286053 |
rs150338627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351888 | CATGATGGTGGGTGC[C/T]TGTAATCCCAGCTAC | 286053 |
rs150343373 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247553 | AACACGGTGAAACCC[C/T]GTCTCCACTGAAAAT | 286053 |
rs150354415 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170553 | CTGGGATTTACAGGC[A/T]TGTGCCACCATGCCC | 286053 |
rs150430345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236241 | GAAGTTTCTAGTTAT[A/G]GACCTGGTGGTAGCT | 286053 |
rs150437233 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118219 | GGCATGGTGGCACAC[A/G]CCTCTAGTCCCAGCT | 286053 |
rs150490358 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113493 | TCTAAAAAATAAATA[A/T]ATAAAAATATATAGT | 286053 |
rs150492321 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198526 | ACCAGCCTTGCATCC[A/C]AGGGATGAAGCCTAC | 286053 |
rs150494408 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231293 | ATTAAATGGTTGCTG[A/G]CATCCCTTCAAGACA | 286053 |
rs150496356 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303010 | TGCAGCTCCACACTC[C/G]CCGCATCTTCTGTTT | 286053 |
rs150531647 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250035 | GCTCTTGTTGCCCAG[A/G]CTGGAGTGCAATGGC | 286053 |
rs150545178 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310587 | AATTCCCGGTTACTT[G/T]AAGCCCCCTTTTTTT | 286053 |
rs150546662 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121192 | AGAAGTTATAGGTAG[C/T]GTGCTCAGTAGATGA | 286053 |
rs150547637 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238103 | GGTCCTCATCTCACT[A/G]TCAGCATTGATCCTG | 286053 |
rs150579557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188357 | AGGTACAGTGTAGTA[G/T]TACCATAGCACAGGT | 286053 |
rs150582672 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264225 | TGTGAATTTCATTGA[C/T]ATTTCTTTTTTAATC | 286053 |
rs150583790 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257720 | TTTGTATTTTTAGTA[A/G]AAACGGGGTTTCATT | 286053 |
rs150584164 | in-del | -/G | 0.0648419 | 0.167978 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240148 | TTTTTTTTTTGAGAC[-/G]GGAGTCTTGCTCTGT | 286053 |
rs150598580 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115928 | AAAGAGGTCAATATC[C/T]TCATCCTCACTCCAC | 286053 |
rs150598888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304455 | AGTGTAGAGAGACCC[A/G]GGGCAAGGAAACGAG | 286053 |
rs150610677 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215991 | TAGGAGGTCTTGGCT[A/G]CAGTGAGCCATGATT | 286053 |
rs150629152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148563 | TCCCAACAGATACTT[C/T]AGTGAGTGCCTGTTT | 286053 |
rs150635636 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259075 | ACCCGGCTAATTTTA[C/T]ATTTTTAGTAGAGAC | 286053 |
rs150654394 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315385 | GTGCACTGTAGCACA[A/G]TGAGGGGCTGAGTTT | 286053 |
rs150662105 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212202 | AGGCTCTTTGCTACC[A/G]ACTTTTACCTTGTTA | 286053 |
rs150687800 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250125 | CTCCCAAGTAGCTGG[G/T]ACTACAGTCATGCAC | 286053 |
rs150753772 | in-del | -/TTA | 0.499879 | 0.0077866 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215043 | TTTATTTTATTTTAT[-/TTA]TTATTATTATTATAC | 286053 |
rs150755614 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271778 | CTCATGCTTTTTAAT[A/G]ACTCTGTAATCATGT | 286053 |
rs150787254 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145445 | CAGTTTCTTAATTGA[C/T]GTATCAGGTGACAGG | 286053 |
rs150790033 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228257 | AAATTTTACTTCTTT[C/G]TAAAGTGTTTTGATG | 286053 |
rs150808634 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160151 | CTTAAATTCTGGCTT[C/T]CATGCACTCTAACTC | 286053 |
rs150818912 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177069 | TGTTACTTGCTTTCT[C/T]TTAATAGTTTTCTAT | 286053 |
rs150823623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense | NSMCE2 | GRCh38.p7 | 8:125362091 | AGTGCCTGGAGGTGG[A/G]GACCCAGCCGCTCCT | 286053 |
rs150829888 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091247 | ATGGCATAACTAGAA[C/T]GCAAATCCACGTCTG | 286053 |
rs150830901 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294116 | TTTCAAGGTTTATCC[A/G]TGTTGTAGCATGTAT | 286053 |
rs150842306 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219386 | AAATTTACTCTGGAT[G/T]GAATATTAACACAGT | 286053 |
rs150850640 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106313 | TCACCACTGATCTTA[G/T]CAGAAAAGTCATACG | 286053 |
rs150860642 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337850 | CGGTGAGCCAAGATC[A/G]CACCATTGCCTGGGC | 286053 |
rs150868618 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250934 | ACCTACATTCACTAA[A/G]TCTTTACTAGGTGAC | 286053 |
rs150871303 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173017 | TCACCGCTAGATGTG[A/G]TCAAACCAACAGGTG | 286053 |
rs150877820 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353837 | GCAATGAGCCAAGAT[C/T]GTGCCATTGCACTCC | 286053 |
rs150898484 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287806 | TTCCACCATTCCAGT[G/T]AATCCTCTCTGCAGA | 286053 |
rs150921942 | in-del | -/AAAAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157121 | TTGTGAATCATTGAC[-/AAAAG]AAGAAGGAGGGGGAA | 286053 |
rs150935279 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296839 | CCAAGGTGTACTTTC[A/G]TGGAATAAAAATGAA | 286053 |
rs150938258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223739 | GGAGAAGTTGAGCAT[C/T]TTTTCCATATATTTC | 286053 |
rs150947398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107686 | ACTAATGGTGCAAAT[A/G]TTAAAAAAGAAAAAG | 286053 |
rs150949280 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194006 | TTGCCTCTTTGTATA[C/T]GTTGAAAGAGGAGGA | 286053 |
rs150964562 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340943 | CTCCTTGATGTTCAC[C/G]TTTCATTTATTTTTA | 286053 |
rs150980435 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174770 | ACACCTTGGCAAACC[A/G]TGAAGTCCACTTGAT | 286053 |
rs150988613 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290555 | ATTCTAGGTTATGTA[A/T]CCTCTTTCAGTTCAA | 286053 |
rs151025548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246154 | CTCTGTGACAATTCA[A/G]TCTGCAAAATGAATC | 286053 |
rs151036018 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319698 | CAACACAGCAGTGAA[A/G]ACTACCCAAAATGAA | 286053 |
rs151075764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124214 | ATCCATGTTGCATGT[A/G]TCAGTAAGTACTTTA | 286053 |
rs151094157 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265358 | TCCCAAGTAGCTGGG[A/G]TTACAGGCATGCACC | 286053 |
rs151124259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306666 | AAGCCTTCATATTGC[A/G]CAGTGAATAACCCAG | 286053 |
rs151128277 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117550 | TTATTTTTATTTTAT[C/T]TTTTTAAGAGATGGG | 286053 |
rs151139526 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136447 | AGAGTGAGGAGTCTA[A/G]GATGACTTTATGTTT | 286053 |
rs151140438 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304820 | TTGAACCCTGGAGGC[-/A]GAGGTTACAGTGAGC | 286053 |
rs151141455 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217963 | AAGGCTCAGGTATTT[A/G]TGGTCATTAAAGCAG | 286053 |
rs151146433 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334692 | AATGAGGCGGTTAGA[A/G]CTCAGAGGATGACTT | 286053 |
rs151148196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261586 | GAAATTTAATTAATA[C/T]ACTTACACTTTGAAT | 286053 |
rs151152542 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250169 | TAATTTTTGTATTTT[C/T]AGTAGAGATGGGGTT | 286053 |
rs151159584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151552 | TCCTTTGAATGTGAG[G/T]AGATTTTTATAAAAT | 286053 |
rs151169645 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198095 | ATTTTGGGCTCAGAC[A/G]ATGGGGTTTTCTAAC | 286053 |
rs151199598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329473 | TTTGAACAAGCATCA[C/T]GTTTTGTTTACATTG | 286053 |
rs151201534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096814 | TGGGGCTTCACCATG[C/T]TGGCTGGGCTGGTCT | 286053 |
rs151236231 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280724 | GTTTGGGTCCCAGAC[A/C]GGAGAAAGCCTTTAA | 286053 |
rs151274863 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169112 | CTGAATTTTTATTTT[C/T]CCCTGACTTTCATGA | 286053 |
rs151316941 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112522 | AATGCATAAAGAAAA[C/T]TGTGCTGTGTATACA | 286053 |
rs151319201 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346637 | CTTCTGCTTGGTGAC[C/T]TAGAGATGATCATCA | 286053 |
rs151336713 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242669 | GCAGGAGCTAGAGAC[C/G]TGGGTGAACTACAGA | 286053 |
rs151338705 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163363 | AAGTCTGAATAAGCC[A/G]TAATCATCTTTACTT | 286053 |
rs180703260 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091372 | TGGAAGGATGAGATT[C/G]GGACCAAGCAGCTGA | 286053 |
rs180708981 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109385 | GAGTTTGAGTTGACC[A/G]GTGGGTGTGTTGGAC | 286053 |
rs180715917 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367470 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 286053 |
rs180726314 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343491 | ATTTAAAGTATGAAT[A/T]AGCCAGGCGTGTTGG | 286053 |
rs180732264 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331086 | GCAGGCGGATCACGA[A/G]GTCAAGAGATCGAGA | 286053 |
rs180736811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103039 | TTGGGAGGCCGAGGC[C/T]GGCAGATCACGAGGT | 286053 |
rs180741368 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360037 | TGGAGGTACAGTTAA[C/T]GACATTTGACGACTG | 286053 |
rs180746836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118656 | TCACTAAATTATTGG[A/G]ATTTGGAGCCTGAAT | 286053 |
rs180748954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353816 | TGAACCCGGGAGGCA[A/G]AGGTTGCAATGAGCC | 286053 |
rs180758106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276711 | TTATACTATATACAG[A/T]TGTATTTTTGTTTGT | 286053 |
rs180766663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311417 | TTATTTTTACCTTGG[A/G]CTTTCAAAAACATAG | 286053 |
rs180767228 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322765 | TTAGCAAATTTGAAG[A/C]ATATAAGACTAATTA | 286053 |
rs180771092 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293889 | ATTCACAGAGCTAGG[C/T]AGCCATCACCACAAT | 286053 |
rs180773088 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246244 | GCTGGAGTGCAATGT[C/T]GCAATCTCGGCTCAC | 286053 |
rs180781489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260557 | GCCTGAGTTTCCTCA[A/G]TAAAAAGAATTTGGA | 286053 |
rs180782860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303218 | AGTTCAGCTTTGACT[A/C]AGGAGAGCCTGTGGG | 286053 |
rs180806992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225419 | ACTGCTAAATAGTTA[C/T]TCAGAGCCCTGCAGC | 286053 |
rs180820203 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193513 | TAGCATTATGCTTCT[A/G]CCTTGTCTCTTTATC | 286053 |
rs180838195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157824 | TTACTGGGCCTTAAT[A/G]TGCCTCTAGTGCAGC | 286053 |
rs180853815 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207094 | TTCATATTCAAAAAT[A/T]CAAAAACTAAGTTCC | 286053 |
rs180861994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347925 | ATGCTTACATTTAAG[A/G]GGGTGGTAGAGTTGT | 286053 |
rs180863637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183677 | TATAGTATCTGGCAC[A/G]TGGACCTGTGATTAC | 286053 |
rs180865539 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198845 | GTTGGTAAGCTATTA[G/T]TTACTGCCTCAATTT | 286053 |
rs180868523 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174671 | TGTTTAAGCTTATTC[A/G]TTTTCACAATTTTTC | 286053 |
rs180878400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166298 | TTTGAGACAGAGTCT[C/T]GCTCTGTCACCAGGC | 286053 |
rs180887034 | snp | A/G/T | 0.00438524 | 0.0466503 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138301 | TGATCATAGCTGACT[A/G/T]CAGCCTTGAATTCCT | 286053 |
rs180889727 | snp | C/T | 0.168135 | 0.236216 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257556 | TTTTTTTTTCTGAGA[C/T]GGAGTCTCGCTCTGT | 286053 |
rs180900302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309015 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACCTGA | 286053 |
rs180906935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326221 | GAGATTGCGCCACTG[C/T]ACTCCAGCCTGGGCA | 286053 |
rs180911394 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363743 | TTGAGACTTCACAGC[A/G]TAGGGGGACAGGCTG | 286053 |
rs180919967 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203144 | TACATAGATTTAAAT[A/T]GAAAAAAATGGTCTT | 286053 |
rs180922125 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221083 | GTCATACCCACCCTC[A/T]ACTGCTACATTTCCA | 286053 |
rs180923054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272987 | TGGGTGACACGGGGC[A/G]GGATCCTGATTCTGC | 286053 |
rs180934632 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188239 | AGTTGGTGGCTTTTC[C/T]GTCTCCTTCAGCATC | 286053 |
rs180939624 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171579 | CTCAGTACCTTGCCA[A/G]TAATAAATAGTTGAG | 286053 |
rs180943441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153968 | AGTCATATAGGATTA[A/T]GTATAGGCTACTTAA | 286053 |
rs180947984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248869 | AGGGCACTCAGGTAT[A/G]ATAATTGGCAGAGCC | 286053 |
rs180956921 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134778 | TGTTGCTCAGGCTGG[A/G]GTACAGTGGCATGAT | 286053 |
rs180976372 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210896 | ACTATGCCCGGCTAA[C/T]TTTTTTTGTATTTTT | 286053 |
rs180984639 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179092 | AAGCCACCTAATCTG[C/T]GGTACTTTGTTATTG | 286053 |
rs180998169 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229232 | ATGGGAAAGAAAAGA[C/G]AGATGCAAGAGACTG | 286053 |
rs181006382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196184 | CCACCAAGTGCAGCC[A/C]TGGATAACTTTTTTT | 286053 |
rs181012397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143341 | GATTAGGAAATACCC[A/G]TATTCTGTTTCAGAA | 286053 |
rs181024367 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160655 | CGCACCCTTTAATAT[A/G]TGATCATTAATAGTG | 286053 |
rs181033820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260447 | CTCTATACTTTCGTG[G/T]GTGGTAGTTGCTTTC | 286053 |
rs181034388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125053 | CCCTGCCTCAGCCTC[A/C]CAAAGTGCTGGGACT | 286053 |
rs181041011 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225019 | ATTAGTGATTATTTT[A/G]GAGTACTTTTGCTAA | 286053 |
rs181045663 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245690 | GAAAAACAATAAAAT[G/T]ATCAATCTAAGAGCT | 286053 |
rs181047952 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206485 | AGTACTGATGATATG[C/T]TGAACTGCCATGGGC | 286053 |
rs181057217 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193237 | CAAAATTAAAACCTC[C/G]AACTTATCACGACAG | 286053 |
rs181061869 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149890 | TCAGCCTTTTCTCCT[A/G]TGATCTGCTCATTCT | 286053 |
rs181064760 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125129998 | CAGACTTTATTTGGA[G/T]TTCACTGATATCCTT | 286053 |
rs181066342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174186 | AATAATCTGCTTGAT[A/T]ATTTGAATATTTGTT | 286053 |
rs181067963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157497 | CTATTTCTGTGATTA[C/T]TGGTAATTAACTTCT | 286053 |
rs181099340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235877 | GAAATAAAAGATGCT[A/T]GCCTTCTAATCCCTA | 286053 |
rs181115058 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199910 | TCTTCTTGTTGAATT[C/G]ATCCCTTTACCATTA | 286053 |
rs181116737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184933 | TAGAAAATAGAGGCC[A/C]GAGAGAGAGACTTGC | 286053 |
rs181122100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167519 | AAAATACAAAAATTA[A/G]CTGGGTTCGGGAGGC | 286053 |
rs181156846 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137682 | TGACATAGAAATGTT[G/T]ATGCCCAAAGGGTGG | 286053 |
rs181165961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121752 | AAATGCCTTATGTGT[A/C]TTCATTCATTTAATC | 286053 |
rs181185237 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102757 | CCCCAAGGAGCATAC[A/G]ATCTAAAGTATTTGA | 286053 |
rs181192639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117987 | TTAAAGACCGCATTC[A/G]ATTTTTGTGTATGAA | 286053 |
rs181201323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133841 | GAGTCTCAGAGAAAA[C/T]GCCGTTTATGATTTT | 286053 |
rs181267803 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356765 | AGAAGCCCTGCACTA[C/G/T]CTAATTGTAATGACT | 286053 |
rs181300617 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097603 | GCCTATGTCTCCCCT[G/T]TTGTGCCTATAATCC | 286053 |
rs181381859 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359334 | TTGCTCTTTCTCTTT[C/T]TTTTTTTTTTTTTTT | 286053 |
rs181382524 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342629 | GCTCCTTCCTTCCCT[C/G]CTCCCTCCCTCCCTC | 286053 |
rs181388737 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105370 | ATAAAATCTTAAACC[A/G]TAAGAGAGAAGACTG | 286053 |
rs181391902 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302681 | CAAATGGCCTGTCCC[A/G]AGAAAGGACCCTGAG | 286053 |
rs181407567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284071 | AGGCAGGAGAATGGC[A/G]TGAACCTGGGAAGCA | 286053 |
rs181416465 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322205 | GACCGTGTCTCTACA[A/G]AGAAATTTTAAAATT | 286053 |
rs181442910 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293482 | TGACTCCAGTGGGTT[A/C]ATTTTGAAATTTATT | 286053 |
rs181450689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269714 | GCTTGGAAAGCAAAT[C/T]GTTTAAGTCTGTGTT | 286053 |
rs181512280 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297553 | AGGGTGAAATCTCTT[A/G]ATTAACAAACACTTA | 286053 |
rs181513197 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356432 | CTTCTGGGTTCAAGC[G/T]ATTCTCCTGCCCTAG | 286053 |
rs181517172 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363347 | GTCTCTACCAAAAAT[G/T]TTTTAAAAATTAGCC | 286053 |
rs181519881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113289 | GGCCAAGAGTTTGAG[A/T]CCACTCTGCACAACA | 286053 |
rs181523031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308453 | ATGGTAGCATTTTAC[A/G]CTGTTCTGGTTACTA | 286053 |
rs181530072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325399 | TCTGTCACCCAGGTT[A/G]GAGTGCAGTGGCACG | 286053 |
rs181532725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250436 | GTTAGACTACCTCTA[C/T]TGATATATTGCTGTG | 286053 |
rs181533507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316128 | TCATTCTTATCAATG[A/C]ATGATGATAACAGAT | 286053 |
rs181534344 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281846 | CTGCCTCCCAAAGTG[C/T]TGGATCACAGGCATG | 286053 |
rs181536925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265044 | AGTAATCAAGTAATA[A/T]TTTATGTAGTATCTT | 286053 |
rs181540241 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230309 | CTAATACCCTATAAA[A/G]CCTTACCCAGAACCC | 286053 |
rs181546362 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170445 | CTCTCTTGGCCTCTT[A/G]GGCAGGCTGGAGTGC | 286053 |
rs181549968 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196706 | ATTTATAATCCTTTG[G/T]GTATATACCCAGTAA | 286053 |
rs181550322 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153773 | AATGTATATCAAAAT[G/T]CTTTGGCATTCATCA | 286053 |
rs181564079 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353904 | CTAAAAAATAAAAAA[A/T]ATATATATATATAAT | 286053 |
rs181591629 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276480 | CACACTAATTTTTCT[A/G]CTTGGCCTACCTTCC | 286053 |
rs181595360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311231 | ACCAAAGAATAGAAA[C/T]CATGAAGAAAACCAC | 286053 |
rs181598505 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253998 | TCAAAAGGCCTAGAA[G/T]ATAACAAATATTTGT | 286053 |
rs181625355 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301853 | AGTTTTAGTAGAGAC[A/G]GGGTTTCGCCGTGTT | 286053 |
rs181634664 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321282 | TTCTTAATATTCTAA[C/G]CTCTGTAATCATTGA | 286053 |
rs181642884 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288883 | CACTGCAGCCTCAAC[C/T]TCCCAGGCTCAAACC | 286053 |
rs181644862 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096245 | TACAGTCATAGGCCA[C/G]AGCTAACTTCAAGGA | 286053 |
rs181654010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283882 | AAGTAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 286053 |
rs181655322 | snp | C/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253448 | ATTCCTGCAATATAC[C/G/T]TTAGATGCAGAGTTT | 286053 |
rs181660087 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269333 | CTCAAGTGATCACCT[A/T]CCTCCGCCTCCCAAA | 286053 |
rs181666238 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235217 | CTGCACTCCAGCCTG[A/C]GCAACAGAGTGAGAC | 286053 |
rs181672291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199822 | GTCTAAGTCTCTTTG[C/T]AGATCTCTAAGGACT | 286053 |
rs181676724 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217268 | CTTTTGAATCTCCAC[G/T]GTAATTTTCAGGGAG | 286053 |
rs181685307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257336 | GTGCCCACAAAAGAG[A/G]TGGGAAAAGAATGAT | 286053 |
rs181688063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220150 | GCTTGTTGGCTGACT[G/T]TGGGAAAACCTATGA | 286053 |
rs181696073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163083 | CAGTTTATACTTTCT[A/G]AGGCCAGGCTTGGTG | 286053 |
rs181698201 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336644 | TTCACATGGTTGGGT[A/T]CACAGTTTCATCTGC | 286053 |
rs181700558 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187990 | AGATAATTGCAGCTA[C/T]AAGTGAAGGTTATAA | 286053 |
rs181731165 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311886 | GAGTTCGAGACCAGC[A/C]TGACCAACATGGTCT | 286053 |
rs181744038 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277581 | GCGCGATCTCAGCTC[A/T]CTGCAAGCTCCGCCT | 286053 |
rs181755629 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341517 | CTGCCTTGCCCTTTC[A/G]GGAACTATTTCCAGA | 286053 |
rs181774593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241142 | CATTTCCTTTGAGCA[C/T]GAGGTCAGTCCTCAA | 286053 |
rs181775419 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211189 | TCTTTAAAGGTTTTA[G/T]CTTTTTTATTAGGTG | 286053 |
rs181777622 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272766 | ACACGTATATATATA[C/T]ACACACACACGTATA | 286053 |
rs181784677 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246485 | CCATGCCTGGCCCCA[A/G]AAATGTTTCTTAAAT | 286053 |
rs181790121 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207924 | TGGACTTGGAAATCT[C/T]ACAGTGTAACTTTTG | 286053 |
rs181791124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180620 | CCAATATCAAGAATT[A/T]TCTGTATCTAACTTG | 286053 |
rs181803376 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179679 | AGTTCTGGTTATGGG[A/G]GGAAAGCACAGTGAA | 286053 |
rs181804596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161248 | GTTGTGGCCAGTGTG[A/G]TATTTAAACCACTAA | 286053 |
rs181814749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143511 | TCTGAGTATATGAGT[C/T]ATGTTGAATTGGAGT | 286053 |
rs181817389 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202343 | TTCCTATTCAGCCAT[C/T]TTGGAACGGACCAGC | 286053 |
rs181839427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144446 | GTAGCCTAGAAAATG[C/G]CATTATACTGAACAA | 286053 |
rs181850194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149564 | AATTTTTATGTTCCT[G/T]TGTTAACTATCTTTT | 286053 |
rs181881867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358704 | TCTCAATTGACTTCT[A/G]ATAACAGTCCCTTTG | 286053 |
rs181910109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112755 | AAGGGAAGGGTGGGA[A/G]GACTGGGGAAATGTT | 286053 |
rs181919574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106146 | CTATTCTGCATATAA[G/T]TCAGCTCTAGGTTTT | 286053 |
rs181920056 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229759 | ATTTTTAGCTACATA[C/T]CTTTAGTTGATTGTT | 286053 |
rs181927650 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149032 | CATTTTGTTGACTTT[C/T]AGAAATTTTCACAAC | 286053 |
rs181931740 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127663 | CCCTGTATCTGCCTT[A/G]TCTTTGTTTTCTGAG | 286053 |
rs181938821 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331723 | GCTTCAGAACCCAAA[C/T]CCCCTGCAAGGAATG | 286053 |
rs181981742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133033 | TGACAGTTGCAGATA[C/T]CCTGATTCAATCCAA | 286053 |
rs181989567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326713 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCAG | 286053 |
rs181996135 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349641 | CCTAATTGAAAAAGT[A/G]CATAGCAATCAAATT | 286053 |
rs182006882 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274250 | AAATACAGAAAATGA[A/G]ACAAAAAAAAACTTT | 286053 |
rs182011648 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092031 | GGGACACTCCACGGG[G/T]ACTCCGAGCCGGGGG | 286053 |
rs182012589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260636 | TTATTTATTTATTTT[A/C]TTTTTTGAGATGGAG | 286053 |
rs182015163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309481 | TAATCCCAGCACTTC[A/G]GGAGGCCAATGGGGG | 286053 |
rs182015374 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356007 | CTTTCAGAGTGTCCA[C/T]AAGGTCAAAACTGTC | 286053 |
rs182016588 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294287 | TGTACAGTGGACATT[C/T]GTTTTTATTTCCATT | 286053 |
rs182019203 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289541 | AAAGGGTTTCCTGTT[A/T]CCTTGTCTGTCTTCC | 286053 |
rs182020651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111081 | TCTGTTCTTTCATAC[A/G]TCCACAACTTGTGTT | 286053 |
rs182027706 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257786 | TTATCCGCCCTCTTC[A/G/T]GCCTCCCAAAGTCCT | 286053 |
rs182048746 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226469 | AGAGGTGTACAGCTG[C/T]TCTTCTTGCACTGTA | 286053 |
rs182072501 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095667 | TGGGAGGCCGAGGCC[A/G]GTGGATCACTTGAGG | 286053 |
rs182097512 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166708 | AGAGGACCCAGGGAA[A/G]ACACTTCTGCTACCA | 286053 |
rs182104147 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093001 | GATACTGCTAAATGT[C/T]CCCTTGCGAGAGGGG | 286053 |
rs182110761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111772 | GCCACTGCACTGCAA[C/T]CTAGGCAGTAGAGTG | 286053 |
rs182111440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354572 | GAAAAGCTGGAAGCC[C/T]CGAGGCACTGCACCT | 286053 |
rs182114573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128464 | AAAAGGAAGAAGTCA[A/G]TGGTGATACTCAAAT | 286053 |
rs182131630 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236272 | GTACGGGATAATTAT[C/T]TTCTAAATTTAAAGT | 286053 |
rs182142116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294710 | TTAGAATTATACGTG[A/T]AAAAACATAAAGTAA | 286053 |
rs182148595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332679 | ACAGAATGCTTTGTA[C/T]ACTGCTATAGCAAGC | 286053 |
rs182149138 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217861 | CCACTATACTTAGTG[A/G]CAGTGACCATCTAAA | 286053 |
rs182149926 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313521 | TTTGATGACAGACAG[G/T]CCTTACTCTTGGTAA | 286053 |
rs182154202 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262745 | GGCTTTAGGTGAGAC[C/T]CATTCTGTGTTAGTT | 286053 |
rs182155094 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200378 | GGCCTAGTGGTGACA[A/G]AATCTCTCAGCATTT | 286053 |
rs182156957 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185392 | GCTCACTTCAACCTC[C/T]GCCTCCCAGGTTCAA | 286053 |
rs182167139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279291 | GGTTTTTTCTTATAT[A/G]TATTGCAAATGGTTG | 286053 |
rs182170091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123729 | CCTCATTATAGGATG[C/T]AATTTTGCTGTAATG | 286053 |
rs182175383 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150657 | AAAGTACTAGGATTA[C/T]AGACGTTAGTCACCA | 286053 |
rs182182382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130495 | TGAAATTCTGTAAAG[A/G]GTTTTGTTTTCTCTG | 286053 |
rs182202662 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249648 | AGCAGTGCAATCAGC[C/G]TGGCCCACTTTGAGT | 286053 |
rs182220969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102005 | TTTTCTAACCCATTT[A/G]TCTTGTAGGCTTTTA | 286053 |
rs182230162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107032 | AACTTTCATTTTACC[A/G]TTAGCAACAAATGCT | 286053 |
rs182259343 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153103 | AACTTTTCCCCCTTC[A/C]GGACATTGAGTCACT | 286053 |
rs182267823 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364020 | GCAATCTTGGCTCAC[C/T]GCAACCCCCACCTCC | 286053 |
rs182277404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145492 | AGGCCCCACTGTGAT[A/G]CTTCTCCATGTATTT | 286053 |
rs182284498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126823 | AACTTTGTACCCACA[C/T]ACATCTCCCTTATTC | 286053 |
rs182300034 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298148 | ACCTGTAGTCCCAGC[C/T]ACTAGGGAGGCTGAG | 286053 |
rs182311106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336307 | CAGTTAAATACTCAG[C/T]CCTTACAGTAGTCCT | 286053 |
rs182314477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337060 | TTTGCATGAATTGCA[A/G]CTAATGGTAGAGGTC | 286053 |
rs182314680 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258922 | GTTTTCTGTTTTTGA[A/G]ACAGAGTTTTGCTCT | 286053 |
rs182318984 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275576 | GCCCAGCCCAGCCAC[A/G]CTGGATAATCACCCT | 286053 |
rs182320205 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317178 | AGACTATGATTTAAA[C/G]TCAGTGGTTTCCTAA | 286053 |
rs182326100 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296917 | CAACAGTGCTTATAC[C/T]GATTTTTCTTTAAGA | 286053 |
rs182326963 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222920 | GAAAAGAAATAGCCA[G/T]GTGTGGTGGTGTGTG | 286053 |
rs182328614 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243814 | ATGGAGCATCCGTCA[C/T]CTTAGGCATTAGAGG | 286053 |
rs182331348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264394 | GCCTGTCCCAGGACA[A/G]GGCAGGCTGTTCTTG | 286053 |
rs182332207 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282210 | CCTCCCCCACCCAGG[C/T]TTAAGCGATTCTCCT | 286053 |
rs182334935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205440 | AATATTTGACATGCA[A/T]TATACTGTCCCTTAT | 286053 |
rs182340343 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190882 | ACATTATTATGATTA[A/T]TTTTTGAGATGGAGT | 286053 |
rs182351057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172982 | GCCTATATGGAGTTA[G/T]TTCTATCTTCCATTA | 286053 |
rs182451288 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284468 | AAACAGAACCAGAGA[C/G]GTTCTATCCTTATCG | 286053 |
rs182468995 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254409 | AAAGTAAATAGTGTC[A/C]CCTTTTACAAGAAAG | 286053 |
rs182495118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195199 | GGCGTCAATATCAAC[C/T]GTGAACATTAAAAAA | 286053 |
rs182496743 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193870 | GCCTCATAATTACCC[A/T]TTGTTATTCTCTGTT | 286053 |
rs182497960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138480 | ATCCTCCTGCCTTGG[C/T]TTCTCAAAGTGCTGG | 286053 |
rs182499014 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116253 | TTTGGACCAAGGTCA[C/T]AGCTAACAAATGGCA | 286053 |
rs182502179 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176300 | ACTTTTCACTTCTTA[C/T]TTAGTTTCACTTCTC | 286053 |
rs182521485 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159452 | TACAGTATTCAGTAT[A/G]GTAACATGCTGTACA | 286053 |
rs182584268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099682 | TAAGTCTTTTCAGGT[G/T]ACCTTGACAAGAGCA | 286053 |
rs182601860 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281306 | TTCTAGTTTTGGAGA[C/T]AAAATCAATTTGAGA | 286053 |
rs182602186 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361680 | TAGCAAAAGCACTTA[A/G]TTGAAAGCTCTTTTG | 286053 |
rs182615308 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250962 | GACAGTAAAACAACA[G/T]GCACAATATGATCCT | 286053 |
rs182621610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323562 | TTCCACAAACATGCA[A/G]AGATAATGCAGTGAG | 286053 |
rs182627392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213030 | GATCCAAAAATTATA[C/T]TGAGCAGTAAATGAT | 286053 |
rs182640439 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344238 | ATCCACCCTCATTGC[C/T]GTCAGTCCTACTTAC | 286053 |
rs182642376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155478 | ATAGTTGAGTAACCT[A/G]AGATTGGTCAGTGAT | 286053 |
rs182644904 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181081 | GAAAGGGCCAGTGAT[C/G]AAAGGGAGCGATTAT | 286053 |
rs182659258 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120270 | AAGGGCAAGAAAGCA[C/T]AAGGATATTTAAATC | 286053 |
rs182709128 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247175 | CTCCAAAAAATAACA[A/C]AAAAAAAATTAGCTG | 286053 |
rs182736248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364378 | ATGTTGGACTGTTGG[A/G]CTTCCTACCACTAGA | 286053 |
rs182740323 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318543 | CCACACATAGACCCA[A/G]AAGTATGTATACAGT | 286053 |
rs182741037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270772 | GGAACCACCAGGTTG[C/T]CTAAGGAGGGGTGAA | 286053 |
rs182752445 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209125 | TTTGATTTTCTATCG[G/T]CAGCTATTTGTGTAC | 286053 |
rs182754443 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283106 | GAAAGAGTAATAATA[A/T]CTACATCATAGAGTT | 286053 |
rs182759012 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178354 | TGAGTAAGCGGGTGG[C/T]ACAGAAAAATCTGAC | 286053 |
rs182759165 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327002 | GCGAGGTGGCTCACA[C/T]CTGTAATCCCAGCAC | 286053 |
rs182765571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350952 | AGAGGGCTGAGCAGG[C/T]GGCAGTAGTGGTTTG | 286053 |
rs182770138 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299429 | AAGCAAGGAATGTCT[G/T]ACATGGCAACAGGAG | 286053 |
rs182778173 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252267 | GGCACAGTGGCTCAC[A/G]CCTATAATCCCAGCA | 286053 |
rs182779394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140246 | TAAGTGAAGAAGAAG[A/G]TTTGTATTGGGAATA | 286053 |
rs182783503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266787 | TTGTGTTTCCTTGCA[A/G]TTCAGGCTTAGTAAA | 286053 |
rs182797617 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294467 | TCACCAGCACATGTT[A/G]TTGTCTCTTTTTTAT | 286053 |
rs182801095 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139908 | GATACAATTTTCATC[G/T]TGAAACTTCCTGGGA | 286053 |
rs182822450 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262281 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCAGG | 286053 |
rs182822733 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277997 | TTAATATGTTAGATA[C/T]GGTATCAGTGGGAGA | 286053 |
rs182833535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227087 | CAGGGTCTGTATTAG[A/G]ATTAACCTTTACTAA | 286053 |
rs182836978 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246698 | CTTGTGAAACTTTGC[A/G]TTTTATTTTATGAAG | 286053 |
rs182851103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208649 | ATGATTGAGTGCCAG[C/T]GTAAGTGTTTCATAC | 286053 |
rs182863141 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290625 | TTCCAGTCTCACAGA[A/G]AAGTTGGTTGAGGCA | 286053 |
rs182871184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114534 | TACGTACATATGTAT[A/G]TACAGCAGTGGGTGA | 286053 |
rs182879530 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265476 | TCCACCCATGTCGGC[C/T]TCCAAAAGTGCTGGG | 286053 |
rs182888916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285187 | ATTTACCTTAAGCAG[A/T]CTTTGTTAGCAAACT | 286053 |
rs182896844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271444 | TGGAAATAAGAGACA[A/G]AGTAGAGTCAAGGAT | 286053 |
rs182899246 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303638 | TGCACTGTAAGTACT[A/G]TTAACTATATATTCC | 286053 |
rs182904634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231413 | AAGGGATTAAAGCAT[C/T]TGAAGACCTTTGTTT | 286053 |
rs182909762 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254900 | GTTTTACAACATGTC[C/T]CCCAAAATTATTTGA | 286053 |
rs182911949 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197048 | CTTTTTAATGGGGTT[G/T]TTTTTTTCTTGTAAA | 286053 |
rs182918298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218286 | GCTGAGGATTCTGAC[A/G]TACAAACAGACAGGT | 286053 |
rs182923419 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106499 | CCTGACCAACTTGGT[A/G]AAACCCCATCTCTAC | 286053 |
rs182926911 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237673 | TTTTTTTCTCAGTAC[A/G]TCAGTGTCTTGTGAG | 286053 |
rs182931292 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136122 | TTTTAATTTTTATTT[C/T]TTTGGTTGTTTGAGA | 286053 |
rs182941672 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163904 | TAACCATAAATAGTT[C/G]ATTGTGATCCAATTT | 286053 |
rs182976132 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309970 | GAGAAACTCAAGATC[A/G]TGAAACATGTAAGCT | 286053 |
rs182977805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189929 | TCAAACAAATTGATG[A/G]AGTTTGCTGGCTCTT | 286053 |
rs182980615 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172219 | TGCTGCACCTCCCTC[A/G]TGTCATTCTCAAGAA | 286053 |
rs182991260 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154734 | GACCAACATGTCATA[A/G]AAGTGTTTTTAGAGC | 286053 |
rs182992638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351352 | TGTACATTTTGTGAC[A/G]TAAAAAAAAAAAAAC | 286053 |
rs182999471 | snp | A/G | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092344 | TTTATGGCATTCTGT[A/G]GGTGACCGAGAAATG | 286053 |
rs183001114 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135802 | GCACACTATCTTGAT[G/T]ACTGATGCTTTATGA | 286053 |
rs183013827 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119926 | TTATTATTTATATAT[A/G]TAAAGCATTATTTAT | 286053 |
rs183078776 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146737 | AACGTCACACACTGG[A/G]GCCTGTTGTGAGGTG | 286053 |
rs183085509 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158703 | TTATTTTAGATGTCA[A/G]TTTAACTTCCTTCCA | 286053 |
rs183086143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125127004 | GCTTTTGGCTCAGAA[A/T]TGATAATGTACATAA | 286053 |
rs183109599 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123512 | GCTCGAAGGGTTAAG[A/T]GACTTATCTGAAGTC | 286053 |
rs183110997 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175231 | TGTGGGCCAACTTCC[C/T]TAAATGTCTTGGTGC | 286053 |
rs183117478 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158165 | CAGCACTTTGTGGCA[A/G]AGTTTCTTGTGGCAT | 286053 |
rs183125112 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138604 | GTAGTATTATCATAG[A/C/T]CTTCGTTGTTTAACT | 286053 |
rs183137858 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123232 | GGGTTACTGAAAAAT[C/T]TTACCTATAAAGTTC | 286053 |
rs183147514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271626 | ATGAAATGGCTTTTG[A/G]CCCCTTAAAACTGAG | 286053 |
rs183155436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331868 | CAGTGGAAGAAGTCT[A/G]GTCTGGGTACTTCTT | 286053 |
rs183156949 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239634 | AAAAAAAAAAATTCA[A/C]ACCAGGCACTATTAA | 286053 |
rs183162035 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106922 | AATCGCTTGAACCCT[C/G]GGGGCGGAGGTTGCA | 286053 |
rs183212222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201696 | CTCAGAGCTCAGTCG[C/T]TGTGCTGAGAGAACC | 286053 |
rs183218904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343852 | ATAAGAAAAATAAAA[A/T]AAAATTAGCTGGACG | 286053 |
rs183225383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323244 | ATTGATCTGTTGATT[C/G]AAAGAAACCACAATC | 286053 |
rs183237464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365384 | ATACCACCCTCAGCC[A/G]AGCTGCCCTCACCTC | 286053 |
rs183258309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357521 | TGAAGGATCCGGGAC[G/T]AAAGTCATGGCCTAC | 286053 |
rs183273143 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327457 | TGGGTTAGAAAATTG[A/C]TGTTGTGGGTTTGTC | 286053 |
rs183324982 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289926 | ATGTTTATAAGAATA[A/T]TTATTTTCTCCCCTG | 286053 |
rs183326513 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114631 | GGGGAGCATGTGTGC[C/G]CTGGCCTCTAGGTGT | 286053 |
rs183349229 | snp | A/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222234 | GTAGGAACGATTTTT[A/T]AAAATTTTTTAATTG | 286053 |
rs183374833 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354113 | ATTTTTGTATTTTTA[A/G]TAGAGAAGGGGTTTC | 286053 |
rs183395310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312634 | TGTCTTAAATAAGTA[A/C]ATAAACAAATAAATA | 286053 |
rs183417205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286968 | GGGAGGTGAACTCCC[A/G]ATCTCACTGTAACGT | 286053 |
rs183420795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126505 | TCAGGTTGGGCCTTT[C/T]CAAGAATTTTACCAC | 286053 |
rs183427141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256381 | TAGATGCCAGTGCCA[A/C]CAGAAGGGAGTGAGG | 286053 |
rs183430522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231814 | TAGTTATCAGTTTAT[A/G]AATCTGTTCTCTCTA | 286053 |
rs183436806 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213339 | ATTCTCTCTTGGCCA[A/G]AGGTTTAGCTGTTTT | 286053 |
rs183446119 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186039 | GGTCAGTAAACTCTG[A/G]GCCATGGACCGAATT | 286053 |
rs183449814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181556 | ATATTGGGGATGGAG[A/G]AGAACATGGGTTGAG | 286053 |
rs183451311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197822 | TTCTTCCTATCCATG[A/G]GTATGAAATGTTCTT | 286053 |
rs183452051 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242729 | TTTGAAATGTCTGGA[G/T]CCTCTGGTAATTACA | 286053 |
rs183460237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336101 | GACCCCACTCCTGGT[A/G]GAAAGGAACCATTGA | 286053 |
rs183465166 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351904 | TGTAATCCCAGCTAC[G/T]TGGGAGACTGAGGCA | 286053 |
rs183465518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315321 | CCCCAGCTTCCACAT[C/G]AGCAAAGTGGGAAAG | 286053 |
rs183473263 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355722 | AAAAAAAAAAAAAAA[A/C]GCTATTGATCTTTAA | 286053 |
rs183474191 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365905 | CAAAGCCCCATTGGC[A/G/T]CACTGACCTCACTTC | 286053 |
rs183489703 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296522 | GCCTCAGCCTCCCTA[A/G]TAGCTGGGATTACAG | 286053 |
rs183490301 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338485 | GTCCTGACAGCAGAG[A/T]GCAAGCATCTATTGC | 286053 |
rs183499977 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185553 | TCAGGGGATCCACTC[A/G]CCTCAGCCTCCCAAA | 286053 |
rs183524086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151065 | AGATGTAATAGCTCT[A/G]CAAAATTATTTAGAC | 286053 |
rs183536979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309588 | TAATTAGCCAGGCGT[A/G]GTGGCACATGCTTGC | 286053 |
rs183548978 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275101 | TCTTCCCTATCCCTG[C/T]TTTTATCTGGTATGA | 286053 |
rs183557422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100242 | TCTAGTGAGAGGAGT[C/T]GTAAAAGAGCATAAT | 286053 |
rs183572408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243467 | CATAGCAAATGGGCT[C/T]CTTTGAAGCAACCTT | 286053 |
rs183594442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204795 | GTCCCCTCTCCATTA[C/T]TTTCTGCCCCCACTA | 286053 |
rs183622949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206518 | ATTGGAAAGGAGAGA[A/G]TGAATGCAAGAAGTG | 286053 |
rs183648329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203810 | GTGGGGTTGTTGAAA[A/G]GTTTTTAGTAGGGTT | 286053 |
rs183652829 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271897 | ATATCTCTGTGAGTT[C/T]ATAGGTGGGGATTAT | 286053 |
rs183654975 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171794 | GAGTGCTTACCAAGT[A/T]CTAGAGAGTATTCTC | 286053 |
rs183667422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256775 | TTAAAAATACAAAAA[A/T]TCAGCTGGGCGTGGT | 286053 |
rs183674728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135028 | CCCTCCCACCTCAGC[C/T]TCCTGAGTAGCTGGG | 286053 |
rs183680863 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240162 | ACGGAGTCTTGCTCT[C/G]TCTCCCAGGCTGGAG | 286053 |
rs183686366 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202002 | GAGCAAGGCTCCGTC[A/G]GCATGGGACCTGCCA | 286053 |
rs183687521 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111571 | TTGGGAGGCCGAGGC[G/T]GGCGGATCACTTGAG | 286053 |
rs183687997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218797 | CTGTTTCGCAACAAC[A/G]TGAATAAACTTGACA | 286053 |
rs183704832 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187324 | CTGAGTTAGGGAACA[A/G]TTTCACAGAGAAGAA | 286053 |
rs183706068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169213 | TCTTCACTCAGTAAA[A/G]CCTGCTATTCCTACC | 286053 |
rs183709320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095463 | TGGCCAAGTGGTGGC[A/G]CGCGCCTGTGGTCCC | 286053 |
rs183712852 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153021 | GAGATCACGCCAGTG[C/G]ACTCCAGCCTGGGCG | 286053 |
rs183715692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112393 | AGCAATCCCAGTAAT[C/G]GGTATGTATCCAAAG | 286053 |
rs183727096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200761 | TGGATAATATCCTGA[A/G]GAGTTTTTTCCAACT | 286053 |
rs183750810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168403 | CTTTCTCAAAGACAA[A/G]TGGACATTTGTCTTG | 286053 |
rs183763486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130933 | TCAGAATTATTAGCC[C/T]GTGCTTCTGTGACAA | 286053 |
rs183823092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355072 | CAAGATATTTCATCA[C/T]GCTTATGCAAATATT | 286053 |
rs183835145 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165908 | ATATTAATTATAGAG[A/G]AAGCAGTGCCAGAGA | 286053 |
rs183849588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148650 | CTTTGTTCAGGTTAC[C/T]AGCCTTACCCACTTT | 286053 |
rs183851609 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280756 | TGTCTATAGATTCTT[A/T]AAGACATAGGAGTCA | 286053 |
rs183855324 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127512 | TAGACTAAAATAGGC[A/G]TTTAAACCAGTTAAC | 286053 |
rs183871003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189315 | GTCCTGCATCCATTG[C/G]CTGGAGCTGAACCTC | 286053 |
rs183874261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314392 | CCTCCCAGATTCAAG[C/T]GATTCTCCTGCCTCA | 286053 |
rs183893102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154102 | ACCCACTGCTCTGTC[A/G]TAGACTTTTGCAAAT | 286053 |
rs183943021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293630 | GGTAACAGGATTACC[C/T]TAAACATTATGAGGT | 286053 |
rs183950522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276601 | GATTGTATATACAGT[C/T]CCTCATAGAGTGTCT | 286053 |
rs183951392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319314 | ACCCACAATGTCTAG[A/G]TTCCAGGTAAAATTA | 286053 |
rs183963657 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358185 | TAAAAATACAAAAAT[G/T]AGCCAGGCTTGGTGG | 286053 |
rs183963738 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338792 | CTAGGAGTAATAAAT[A/C]TGGTATGCATGATGA | 286053 |
rs183973961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260450 | TATACTTTCGTGTGT[A/G]GTAGTTGCTTTCCCC | 286053 |
rs183979123 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299892 | GGCAGAATCTCGGCT[C/T]GCTGCAGCCTCCACC | 286053 |
rs183981728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225104 | ATTTATCACATATTT[A/G]GCATATCTTTCTTAG | 286053 |
rs183984827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131616 | ACGTGGAAAAAAAAA[A/G]TGCTTGGAGATTGTA | 286053 |
rs183985093 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245802 | ACTTTGGGAGGCCCA[C/G]GCAGTGGATCACCAG | 286053 |
rs184007809 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337871 | TTGCCTGGGCAAGAG[C/T]GAAACTCTATCTCAA | 286053 |
rs184013926 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334115 | AAAGGGCCATTGTGA[C/G]GTTAAATTAGTTAAA | 286053 |
rs184027461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295703 | TGTGATTGTGTGGCT[C/T]GGTTGGGGAATAGTT | 286053 |
rs184030051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299137 | TTGAAGTATTTTTAT[A/G]GCATCACCTACACAT | 286053 |
rs184042574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103134 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 286053 |
rs184049645 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360329 | GTTATCAGTATAGAC[G/T]AGTCAACCCGCTCAA | 286053 |
rs184087639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280859 | TTATAAACTGGTGTA[A/G]TTAATCTGTAACTAT | 286053 |
rs184098582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362234 | CGGAGACAGTTGTTT[C/G]TCCAGAGGAGGCATG | 286053 |
rs184099543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314696 | AAGTGGAGCTGTGAT[C/T]CTGCCAGTAGCTTTC | 286053 |
rs184104412 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295940 | AAACTACTGCATAAT[A/C]CTGAACCATGTGCCT | 286053 |
rs184106621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248302 | ACAATAAAGACAAAA[A/G]CAATTGCTTCAAACT | 286053 |
rs184110913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263875 | TTTTTGTGTTTTACT[C/T]ACTGCTGTCTCCCCA | 286053 |
rs184114066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229001 | TGATAGCCTTGAAAA[C/T]TGTTAGGGTGTTGGG | 286053 |
rs184137133 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125195969 | TCGGCTCACTGCAAC[C/T]TCCAACTCTTGGGTT | 286053 |
rs184142476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264321 | CAACAGGATGGAGAA[C/T]ATATGCCTTATGTAT | 286053 |
rs184147194 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324498 | TGAGGACTATTGATA[C/G]ATGCAGCAAGGTGCC | 286053 |
rs184167565 | snp | A/C/T | 6.59385e-05 | 0.00574156 | missense, synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125357247 | TGACAGAGAAGCTGA[A/C/T]GGAACAGAAGGAGTG | 286053 |
rs184171004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287586 | TCTTCTTTCTGTATC[A/G]TCCATATCATTAGTC | 286053 |
rs184172770 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229277 | AGCACTTAGTAGATC[A/G]ATGAACTGAAAGCAG | 286053 |
rs184182220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282662 | AGAGTTGGTAATTTC[C/T]ACTGAGTTCAATTCA | 286053 |
rs184186602 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317688 | ATCTGATTCCAGGTT[A/G]CAGGGGAGAAAAGAA | 286053 |
rs184195817 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196250 | GGTACATGTGCACAA[C/T]GTGCAGGTTTGTTAC | 286053 |
rs184197211 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119182 | TTACCGTGGAATCTC[A/G]CTCCATAAATTTCCA | 286053 |
rs184207975 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093849 | TCGTCCAGGCTAGAA[C/T]GCAGTAGCATGATCA | 286053 |
rs184218736 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160826 | TCTGTGTACGAGTAC[A/G]CAATCATGCTGTTTA | 286053 |
rs184221082 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346285 | TTGGAAATGTTGGGG[C/G]TTTGAAGTAGGACAG | 286053 |
rs184222384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251975 | TCTAAGAGATTTACA[C/T]AATATCACTTTGGTG | 286053 |
rs184232760 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206055 | ATCAAGAGCTTTGTG[A/C]AAATTATCTATAAAA | 286053 |
rs184237663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221710 | TCATTTATGTTTCAT[A/G]TGTAGCTTACACACA | 286053 |
rs184237934 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363366 | TAAAAATTAGCCAGG[C/T]GTGATATTGTGCACC | 286053 |
rs184247565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192548 | GGAAAAAACTGCGTA[C/T]AGAAATTCAGAGCTA | 286053 |
rs184249607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173867 | TGACACTGACTCACT[A/G]TGACCTTGGGCAAGA | 286053 |
rs184256142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131940 | TCAAATCTGGGCAGC[C/T]TGTCTCCAGAGTCTA | 286053 |
rs184257792 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157442 | ACCAGAGAAAGAAAG[C/T]TGACTTTAGGTATTC | 286053 |
rs184261198 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108055 | AAAATAAAAAAAATT[A/T]TGATGAAAATAGTTT | 286053 |
rs184267413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137137 | TTCTCCGACAGATAG[A/G]AATATGAAATGAAGT | 286053 |
rs184275101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121190 | TGAGAAGTTATAGGT[A/G]GCGTGCTCAGTAGAT | 286053 |
rs184275316 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281032 | TATCCAGAATGGGTC[A/G]GTGAATGCAGATGTC | 286053 |
rs184276270 | snp | C/T | 1.65817e-05 | 0.00287933 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102296 | CTTACGAATCTTGTT[C/T]CATTGTGTTTGAAAA | 286053 |
rs184278517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305097 | TCAGAAGTGAAGGAT[A/G]TCTTTATGTTTTCCA | 286053 |
rs184285617 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345713 | GCTAGGTGAAGAGAT[A/G]GCAGCAGAAGCACAA | 286053 |
rs184300068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248897 | GCCAGCAGCCAGGCA[A/C]GGTGGCTCATGCCTG | 286053 |
rs184311932 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210939 | GATTTCACCATGTTG[G/T]CCAGGCTGGTCTTGG | 286053 |
rs184323788 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100817 | CCTCCTGCTTCAGCC[C/T]CCCAAAGTGCTGGGA | 286053 |
rs184329737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115234 | ATGTCACAAATTAGA[C/T]CCTCCCCAACAGCTG | 286053 |
rs184336249 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320311 | GGAAGGAAGGAAGGG[A/G]AGGGAAGGAAGGGAA | 286053 |
rs184345698 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168697 | CTTCCCAGAGGCCTC[A/T]CCTCCTAATACCATC | 286053 |
rs184346103 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179418 | ACATGATTAGCCACT[C/T]AATTTTTTTTCCTTT | 286053 |
rs184357659 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366653 | GCACAGCTTGGTCCT[G/T]ATTTTGACACTTTTC | 286053 |
rs184357998 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252840 | TTAGATGGGTAGTTC[C/T]GGAGTTAAGAGCGCA | 286053 |
rs184358753 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104030 | AATTTTGCTCTTGTT[G/T]CCCAGGCTGGAGTGC | 286053 |
rs184359451 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209818 | AATGACAAGAAATTG[G/T]GAGAATTTATAATAG | 286053 |
rs184363897 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216352 | GCTGAATCAAATGAT[C/T]TGTGGGTCCGGGCGC | 286053 |
rs184364234 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341661 | AGAAGAAAGTGATAG[A/C]CTACAGGAAATTTGA | 286053 |
rs184364520 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321444 | ACTGGCTTCGTGGTG[A/T]ATTCTACCAAGTATT | 286053 |
rs184370913 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195366 | AGTTGTTTACTAGGC[A/G/T]CTCTAAACGATACAA | 286053 |
rs184384906 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178702 | GGTGAAACCCCGTTT[C/T]TACTAAAAATACAAA | 286053 |
rs184386145 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159877 | AGGCAGGAGAATCGC[G/T]TGAACCCAGGAGGCA | 286053 |
rs184389051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182678 | CTATGTTTTCTCTCA[A/G]AAGACCACTTTATCT | 286053 |
rs184391088 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104640 | GGACCCCAGTGCAGA[C/T]TCCTAGAGCTCTTTA | 286053 |
rs184394726 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101472 | GTCTTCATGTTATGT[C/G]TATCTGATTCCATGA | 286053 |
rs184396684 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141814 | CCTCACCAGCTAAAC[A/C]TGTTCTTTCTATAGG | 286053 |
rs184404115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123877 | TTAGCTTTTTTATTC[C/T]TTTATTTGGTGACAA | 286053 |
rs184498506 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234171 | GCTCTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 286053 |
rs184512568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198468 | TTTTTGTCATTGGTT[C/T]TGTTTATGTGATGGA | 286053 |
rs184524910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120779 | TTGAGGCATTTGGGG[C/G]AAGCTCCAAACAGAT | 286053 |
rs184532112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115970 | TTAGGCTCATTGAAT[C/T]GAAACAACTTACCAT | 286053 |
rs184692347 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353003 | TTACCTTTTTATTTC[A/C/G]TGATCACTGATGCTG | 286053 |
rs184711205 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311324 | ATTTAAAACCTAGAA[A/T]CTTTGTAGAAATCTG | 286053 |
rs184765923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283356 | AGTTCAAAACCACCA[C/T]GGTCAACATGACGAA | 286053 |
rs184823839 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330385 | TTCACCACGTTGGCC[A/G]GGCTGGTCTCGAACT | 286053 |
rs184831976 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367407 | GTAATCCTAGCTACT[C/T]GGGAGGCTGAGGCAG | 286053 |
rs184845156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345985 | ACATGGCAAAACCCC[A/G]TCTCTACTAAAAATA | 286053 |
rs184848166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362457 | CAGTGCAGCTGGCTC[C/T]TCTCCACGAGCTTCT | 286053 |
rs184852846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334667 | GGAGTTAGTTTCAAG[A/G]ATGTCTTGAAATGAG | 286053 |
rs184871323 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307805 | TCAATTGCTTAAGAG[A/T]TAAAAACGATTACTG | 286053 |
rs184874216 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308532 | GTCCTTAGTCACCTA[C/T]TTTTGCTGCTGATAG | 286053 |
rs184877301 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288490 | ATTGATTGATTGCCT[A/G]TATCTCCTCAAATTC | 286053 |
rs184877734 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267154 | GATTATATATAGGCA[C/T]GCACTGCCACGCCCG | 286053 |
rs184880592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289282 | AAAGTATCACTCATG[C/T]AGCTGTTGCAGGACA | 286053 |
rs184888243 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324913 | GCAAATTGATGTAAG[A/G]CATCAGAAAACAGAT | 286053 |
rs184890826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273230 | TTTGGTATTGAGTCA[A/G]CCAGATACTGATACC | 286053 |
rs184891399 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272877 | TATACACACGTATAC[A/G]TGTGTGTATATATAT | 286053 |
rs184908861 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257143 | ACAAAAATTAGTCAG[A/G]CGTGGTGGCACGTGC | 286053 |
rs184910912 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272178 | ACCATCATGCCTGTC[A/G]AATTTTTTTGTATTT | 286053 |
rs184912828 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257753 | GTTAGCCAGGATGGT[C/G]TCGATCTCCTGACTT | 286053 |
rs184933953 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203367 | AGAAAGAGGAAGGGA[A/T]GGAGGCAGAAATGGC | 286053 |
rs184938396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221492 | CAAGCAGTCCACCTG[C/T]CTCAGCTTCCCAAAG | 286053 |
rs184946229 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188363 | AGTGTAGTATTACCA[C/T]AGCACAGGTCCTTGA | 286053 |
rs184947901 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178912 | AAAATGAGGTCAGTA[A/C]GTGGGCCTTAATCCA | 286053 |
rs184960555 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171707 | CTACATCTTAAACTT[G/T]CTATAATAATAATAA | 286053 |
rs184964374 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142786 | ATTTTGTATTTTTAG[A/T]AGAGACGGTTTCTCC | 286053 |
rs184965779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289049 | CTGCCTTAACCTCCC[A/G]AAGTGCTGGGATTTA | 286053 |
rs184966520 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108265 | CCCACTGGGGTAATT[C/T]AGCAAGAACTTGTTA | 286053 |
rs184974091 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355281 | ACACATTGAGGAAAG[C/T]CATTTTTATGTCTGT | 286053 |
rs184976207 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325795 | CCACTCTACTAAAAA[C/T]ATAAAAGTTAACTGG | 286053 |
rs185015004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329739 | CAGGCCAGTTTACCT[C/T]TCTGGACCTCGGTTT | 286053 |
rs185015767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310117 | ATTGGGAAACTAATC[A/G]TTTGTGTAACTGGCA | 286053 |
rs185022216 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292280 | TGGGAGGCCAGGGGG[A/G]GCAGTGGCTCACACC | 286053 |
rs185025658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260313 | GTTTTTCAGAATGGA[A/G]TCAGGAGGGTAAAAT | 286053 |
rs185025980 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253187 | ATAGGCAAATATGGA[A/G]GTTTATATACACTTA | 286053 |
rs185026183 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328699 | AATCAGTGATTTGCT[A/G]TCTATCATCGGTGTT | 286053 |
rs185039007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098409 | TTGGCCATTACTCCC[A/G]GTGAGTCAGGAAGTC | 286053 |
rs185040040 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234863 | ACACAACTCTTGTCC[A/G]CCTAATCCCCACCCC | 286053 |
rs185046837 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114062 | ACCTATAAGCACATG[A/C]TCTTCTGAAAATCTG | 286053 |
rs185056115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275866 | AACCCAGAACGCTCC[A/G]CCTGCAAAACCCAAG | 286053 |
rs185060310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259935 | TTGGAGCTGGAAACT[A/G]CATTGGGCTCATGTA | 286053 |
rs185060893 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160556 | GCCAATGCAGAGGCC[A/G]GTGAACAATGTGACA | 286053 |
rs185062233 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216621 | CCTGGGCAACAAGAG[C/T]GAGGCTGTGTGTCAA | 286053 |
rs185070267 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090594 | AATTTGGCGTGGAAC[C/T]GTGATTTTCAGTTTG | 286053 |
rs185070991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183687 | GGCACATGGACCTGT[C/G]ATTACCAGCCTGAGG | 286053 |
rs185074629 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198233 | CACTATGTTGAATAG[C/G]AGTGGTGAGAGAGGG | 286053 |
rs185077340 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166379 | TCAAGAGATTCTTGC[A/G]CCTCAGCCTCCCAAG | 286053 |
rs185081891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124943 | GGGACTACAGGTGCC[C/T]GCCATCACACCTGAC | 286053 |
rs185088015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149200 | CCCCTGACCCCCTAA[C/T]TTACATTGAGATATT | 286053 |
rs185089808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167645 | TCTCAAAAAAAAAAT[G/T]GCAAAGTCAATCCTA | 286053 |
rs185094157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193285 | GGACAAGCTACAACA[G/T]AGGACAAAATATTCA | 286053 |
rs185094187 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149951 | TTAGATTAAGAGTGC[C/G]TTCTCCAGAAAGTAG | 286053 |
rs185100276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165379 | AAACATTTAAATGTC[A/G]TTCTAATATAAGATG | 286053 |
rs185102814 | snp | A/G | 0.000186168 | 0.0096462 | intron-variant, missense | NSMCE2 | GRCh38.p7 | 8:125130279 | TCAAAGCTAGTGCAA[A/G]TCATCAACATGACCA | 286053 |
rs185108149 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116800 | GAGCCACAGAACAAA[A/G]CATAGTGCCTAATTA | 286053 |
rs185115828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127260 | AATTAGTGGAAAAAG[A/G]ATTTAAAGTGTATGT | 286053 |
rs185131834 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310320 | CCTTTTTTGCTCCTC[A/C]GTTTTTTTTAATCCC | 286053 |
rs185144900 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276135 | ACAGGATACTCAATT[A/T]CATTTAGACAAAGAA | 286053 |
rs185148819 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245144 | AAAAATTAGCCCGGC[A/G]TGGTGGTGGACACCT | 286053 |
rs185175330 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219387 | AATTTACTCTGGATT[A/G]AATATTAACACAGTG | 286053 |
rs185190239 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247951 | ATGGGAGAATGACAG[G/T]AAACAGACAACTATT | 286053 |
rs185200755 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187751 | TAGAAACTTTCAAAA[C/T]ATAAGGGCTTTGCTT | 286053 |
rs185206761 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094377 | ATTTATTGGGAGAGA[C/T]TGAGAAAAGTATGTC | 286053 |
rs185208886 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181994 | AGAGATTGTTTTCAA[A/C]CTCACTATCTTTTGC | 286053 |
rs185217507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153151 | AAAACTTCTCACTCT[C/T]TCTCACATTCAGTAG | 286053 |
rs185219238 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148020 | AAGACCCTCTGACTA[C/G]AGTTATCTGACGGCA | 286053 |
rs185222315 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143391 | CGTCCCATTTATTCT[A/G]AGAAATTTAAAATAC | 286053 |
rs185233007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125398 | CAAGCACTTCCATCT[A/G]TTATCACAGAGCGGG | 286053 |
rs185276487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102933 | AAGTTCAACTTTAAT[A/G]AATTTTACCTACATT | 286053 |
rs185286533 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118193 | TCTACTAAAAATACA[A/G]AAATTAGCTGGGCAT | 286053 |
rs185290431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263328 | GGGTCCTCTCTTAGA[C/T]GTTGGAATACTCAGT | 286053 |
rs185308905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202265 | AACCAGGAACCTCAA[C/T]TGGAAATGCCAAAAT | 286053 |
rs185318301 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170291 | CTATTCCATTTTTAA[G/T]TAGACCAAAATCCAG | 286053 |
rs185318329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228400 | CAGTGATGGTAACAT[A/C]TGTAAATATGTGATA | 286053 |
rs185338753 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133302 | TAAAACAAACATTTT[A/T]ATGGAATGCTTTATT | 286053 |
rs185354931 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358994 | GATTTCGGCCAGGCG[C/G]GGTGGCTCACACCTG | 286053 |
rs185367037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136533 | TGGGATGTGATTGAT[G/T]AGAACCTCCCATTTT | 286053 |
rs185372973 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113066 | AGAAAATGGGGGGGG[C/G]GGTGAGTCAATACCT | 286053 |
rs185375174 | snp | C/G | 0.030665 | 0.119967 | utr-variant-5-prime, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091735 | GCAGTCCCGGACCTG[C/G]AGCGGGTCAGACCCC | 286053 |
rs185385667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109422 | GAATGGATTGGGAGA[G/T]ATTAAAGTGCAGAAG | 286053 |
rs185465623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184943 | AGGCCAGAGAGAGAG[A/G]CTTGCTTCTAGATGC | 286053 |
rs185466817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337328 | ATAATTCTTCTTTGT[A/G]GTCCATTGACTCTTA | 286053 |
rs185468692 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357088 | AGCAGAAGAGTTTCT[A/G]TGCATCCAGTCCTTA | 286053 |
rs185473211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365225 | CCTGTTTTGCCCCAT[C/T]GTTTCCCACTGTGAT | 286053 |
rs185505611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317316 | GATCTTCTCTCCCCA[A/G]CCTCCGAATAGCTGG | 286053 |
rs185610645 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313445 | TGGCACGTGGAAAAC[A/C]CTTTAAAGAAGGAAG | 286053 |
rs185615411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188139 | ATAAAAGGAGGGAGC[A/G]GCCATTCACTTTACA | 286053 |
rs185615707 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342744 | TTCAGACAAGACCCT[C/G]AAAACTAAGTACAGA | 286053 |
rs185617800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294611 | ATACTTTCTTATGCA[C/T]GTAATAGAAACTGTC | 286053 |
rs185621438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170988 | CTCCGTCATCTGTCC[C/T]ACTTCGCACCCTGCT | 286053 |
rs185623891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359598 | TCGGCCTCCCAAAGT[A/G]TTGGGATTACAGGCA | 286053 |
rs185631786 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153883 | TCTTCTAAAAAGCAA[A/G]TATTTTGTTTTGCTC | 286053 |
rs185639873 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301046 | ACAATCATTAACTAT[G/T]TTTGTGAAGTATGGC | 286053 |
rs185641936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341183 | CTTCTGCGATGCTGC[A/G]GGAGGGGCACTCATT | 286053 |
rs185643433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133842 | AGTCTCAGAGAAAAC[A/G]CCGTTTATGATTTTT | 286053 |
rs185646329 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322275 | CGGGAGGCTGAGGCA[A/G]GAGGATCACTTGAGC | 286053 |
rs185673568 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268321 | TTGTGACGTATGTGG[C/T]AAAGGAAATTGACAT | 286053 |
rs185692904 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244526 | TAAAAGACAAGGATT[C/T]GAATTGGCTTTTAAA | 286053 |
rs185726713 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205631 | ATTTTCAGAATACCA[A/C]GTTGTGAGAAGCAGC | 286053 |
rs185740160 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358513 | ATATACACACACACA[C/T]ATATATATATCTCAC | 286053 |
rs185740876 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173465 | CCTATCTAATTTTAT[C/T]TGGAACTGAATCTTC | 286053 |
rs185756842 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297620 | AAGATCAGTTAAAGC[C/G/T]AGCAGTTCGAGACCA | 286053 |
rs185757998 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265648 | ACTTTACCCTAGTCC[A/G]TGCCTTGCCTTAGAG | 286053 |
rs185764510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336762 | TGAACAAATTCTTTG[C/T]AAGCACTTCTAGTCT | 286053 |
rs185768356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320788 | GATGCAGTATTAGTT[C/T]TCATACTGCTGTAAA | 286053 |
rs185770312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316961 | TTTTTGGTTTTTCGT[C/T]TTTTTTTTAAGAGAT | 286053 |
rs185787846 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250501 | TTACTGTAAGTAAAC[A/G]TTTATTAACTAAAAA | 286053 |
rs185790014 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281884 | ACAACTGGCTAAGTG[G/T]GTGATTTAAGAATCT | 286053 |
rs185796399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265076 | AAAATTAAAGTTTAT[A/G]TACAGTTCAACAGGG | 286053 |
rs185805087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283783 | AGACCCTAGAGGAAC[C/G]CAGGGCCCATTTTGC | 286053 |
rs185818353 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212417 | ATGACCTCCTAGAGC[C/T]GAGGCAGTGAGAGCC | 286053 |
rs185838053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223228 | CCAGACATGGTGGTA[C/T]ACACCTGTGGTCCCA | 286053 |
rs185849858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134873 | GTTGGGACTATAGGC[A/G]TATGCCACCATACCC | 286053 |
rs185855111 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192042 | GACAAATGAGTCAGC[A/G]GCAAGTTTAAACACA | 286053 |
rs185871712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127721 | TTGGCTGAAACTTAA[C/T]AATACAGGTTGAGTA | 286053 |
rs185878616 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156204 | ATTATACTTCAGCTT[C/T]TATTGTTTTTATTAT | 286053 |
rs185881870 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095874 | GGGACAAGAGCAAAA[C/T]TCCATCTCAAAAAAA | 286053 |
rs185900427 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302091 | AGCCTCCCAGAGCTG[C/G]GATTACAGGTGCGTG | 286053 |
rs185907376 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251209 | TAGCTTTCTTATATA[C/T]TACCCATACCCATTA | 286053 |
rs185907449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309090 | TCTCTACTAAAAATA[C/T]AAAAAATTTAGTTGG | 286053 |
rs185923757 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269459 | ACTGTTTAACTTTGT[A/G]TCTATGGAGCAAAAC | 286053 |
rs185937181 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208565 | GATATTTAAAATAGT[C/T]ATAATTCAAAGCATG | 286053 |
rs185937302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284015 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGCGCCT | 286053 |
rs185939106 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253612 | TAAACATTAGTTTGA[C/G]AATACAGATAATGTT | 286053 |
rs185943995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226491 | TGCACTGTACCCCTC[A/G]TATCTGCAGCCGGGA | 286053 |
rs185947944 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193804 | TTATCCTAAGTGTGC[A/C]CCTTCAGTCTCTGCC | 286053 |
rs185953549 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235268 | AAAAAAGGAAACCTA[A/C]AAGCTTTTCCCAAGA | 286053 |
rs185965719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176031 | CTTCTCCTTGCTGAC[A/G]TAGAGAAATGTTGCA | 286053 |
rs185965999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158322 | TTTTTAAAAACATGC[A/G]GTGAATGCTTAGTCT | 286053 |
rs185971031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154041 | GTTTAAAATAAGATT[A/G]TTTTTTTAAAAGGCA | 286053 |
rs185979921 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138661 | CTGAAGTTCATCTTT[A/C]AAGTGACAAATGAAG | 286053 |
rs185986309 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123383 | CACCTTCTCTCTGAA[A/C]TATAAAGATATGGAG | 286053 |
rs185989156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157689 | GGTTTCGAAGTAACA[C/T]AGCTGCTAATAGGTG | 286053 |
rs186005200 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122247 | ACAAAGATATGAAGA[C/T]ACTTCAACAAATCTC | 286053 |
rs186026945 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105587 | TCATGCTCTAAAGCC[A/T]AAGTTGGCAAAGTTT | 286053 |
rs186041546 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103049 | GAGGCCGGCAGATCA[C/T]GAGGTCAGGAGTTTG | 286053 |
rs186101507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179816 | CTTCACCTCCTCAGC[A/G]GTGGTTGTAGTGGAA | 286053 |
rs186105783 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174284 | CCAAGGCCTAGCATG[G/T]TTCCCACATGTGGTA | 286053 |
rs186116147 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161766 | CACTGCACTCCAGCT[C/T]GGGTGCCAGAGTGAG | 286053 |
rs186122444 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143920 | GGTTCTTTTCTGGAG[A/T]TTAGGGAGGATTCTG | 286053 |
rs186127014 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137689 | GAAATGTTTATGCCC[A/G]AAGGGTGGTGATTAT | 286053 |
rs186130366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125827 | AACAGTGTGAGTATC[A/G]TAGTTCACCTTGTTG | 286053 |
rs186134006 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298316 | TGTTGCAAGTACTTT[G/T]TTTAAGTTAACTCAT | 286053 |
rs186135916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326378 | TGCATATCTCTTTGA[A/G]TAAAAATAGGCATTA | 286053 |
rs186152462 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125363914 | ATTTAACACATCATG[G/T]ACCTGAGTATGTAGG | 286053 |
rs186161034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326724 | ACTTTGGGAGGCCGA[A/G]GCAGGTGGATCACCT | 286053 |
rs186178457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364052 | GGATTCAAGTGATTT[C/T]CCTGCCTCAGCCTCA | 286053 |
rs186180550 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349662 | CAATCAAATTTTATT[C/T]CCAGCTGGCATAAAA | 286053 |
rs186182897 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119002 | ATTTCTTGTAATTTT[G/T]TCCTTCCTCCAGTGG | 286053 |
rs186186250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111609 | GTTCCAGATCAGCCT[A/G]GCCAACATGGTGAAA | 286053 |
rs186190509 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274879 | AGGTTGCAGTGAGCC[A/G]AGATCGCGCCATTGC | 286053 |
rs186198654 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309498 | GAGGCCAATGGGGGA[A/G]GATCGCTTGAGCTCG | 286053 |
rs186208814 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289729 | CCACCTACCTCGAAT[A/T]TAAAGCTTAGGTTTT | 286053 |
rs186231043 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354160 | TGGTCTCGAACTCCT[C/G]ACCTCAGGTGATCTG | 286053 |
rs186267186 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348113 | GTGTGACTGAGCTCC[C/G]TGAAGGCAAGGATTA | 286053 |
rs186273265 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282409 | GTGAGCCACTGCACC[C/T]GGCAAGATCCCTTAA | 286053 |
rs186284009 | snp | A/G | 0.00914312 | 0.0669923 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367494 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGCCTCT | 286053 |
rs186289059 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284149 | ACAGAGCGAGACTCC[A/G]GAAAAAGAAAAAAAA | 286053 |
rs186294579 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106331 | GAAAAGTCATACGCT[C/T]TCAAATTTATAATGG | 286053 |
rs186316460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331403 | CACCTGTAAAATTGT[C/T]ATCAGTACTCAGGGC | 286053 |
rs186323041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311448 | ATAATAAAAACATTT[C/T]ATTTGCTCTAACACA | 286053 |
rs186324710 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092539 | TAATAGGAGTGTGTT[G/T]TGTACATGTGCATGT | 286053 |
rs186325239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254256 | TCTTTTGCATTTTTC[A/G]TATTCTATTTAATGG | 286053 |
rs186328594 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217362 | ATTTATTTATTTATT[A/T]TTTATTTATTTATTT | 286053 |
rs186343398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353838 | CAATGAGCCAAGATC[A/G]TGCCATTGCACTCCA | 286053 |
rs186345589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254482 | TTAACTTGCTAAAAG[A/G]AAGAAATTGAACAAG | 286053 |
rs186347722 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276926 | GGGGACACCATTCAC[A/G]TAGATGACAGTGTGA | 286053 |
rs186362560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294039 | ATTTGCTGTTTGGGA[C/T]GTTTCATATAAACAT | 286053 |
rs186366271 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236793 | TCTATACCACTTGGT[A/T]CACTATCTTTCTTTT | 286053 |
rs186376541 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200650 | TCTGACAATTATGTG[G/T]CTTGGGGTTGCTCTT | 286053 |
rs186379582 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218183 | ATCCCACTTTAGAAA[C/G]CTGTACTGAGAAAGC | 286053 |
rs186383293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351198 | ATAACTGACAAGCCA[C/T]AAAAATTGGGAACTT | 286053 |
rs186394545 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185411 | TCCCAGGTTCAAGTG[A/C]TTCTCCTGCCTCAGC | 286053 |
rs186425762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331899 | GTAAACTTCAGTCAG[A/G]TATGGCCTGTGCAAG | 286053 |
rs186429246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249795 | AAACCTGACATTGTT[C/T]TAGGTTTGGGATGAT | 286053 |
rs186430661 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211283 | CTCCCTGGAAACAGT[C/T]ACTCTTACCAGTTCC | 286053 |
rs186435598 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303131 | ACCAAAGGTTCAGTT[G/T]CCTGTTACTGACCAC | 286053 |
rs186483427 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241310 | TAGAGTGAAAAAGAC[A/G]TTGGCTCACCCATGA | 286053 |
rs186483765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269793 | ATCAGTCATCATCAA[C/T]AGTTAACAACATCTA | 286053 |
rs186495364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235929 | AAGAGTCCACATTTT[A/G]CATATAATGTTAACG | 286053 |
rs186495547 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180726 | TTTGTGAAACTGGGG[A/G]GAGGAGATCAAGATT | 286053 |
rs186500697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202593 | CTAGCCCACAGAGTT[G/T]TTTATGGGTTAAATC | 286053 |
rs186502093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144559 | TATTGCTACAGGCTT[A/G]CTGCCTACATCTCTT | 286053 |
rs186545853 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200059 | CTTTATTTTGAGCCT[A/C]TGTGTGTCTCTGCAC | 286053 |
rs186546875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294367 | TATGTTTATCCTTTT[C/T]AGGAACTGCCAGACT | 286053 |
rs186548518 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261662 | AATCCTTAAGATTTC[A/G]TAACCAAGGGATTTA | 286053 |
rs186549431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146123 | TCCTCCTTGGAAGTG[C/T]TGTTTTATGCTAACA | 286053 |
rs186555798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126831 | ACCCACACACATCTC[A/C]CTTATTCTCACTTTA | 286053 |
rs186562932 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138413 | TTATTTTTAGTAGAG[A/G]TGGGGTCATGCTTTG | 286053 |
rs186569492 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122685 | CTCTTCTTGGGTTCC[C/T]CTTTGTTTGTTGTAC | 286053 |
rs186580672 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356458 | CCTAGCCTCCCAAAT[A/G]GCTGGGACTACAGGC | 286053 |
rs186602839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199853 | TGCTTTATGAATCTG[G/T]GTGCGCCTGTGTTGG | 286053 |
rs186603896 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223107 | ACGGTGGCTCACACC[C/T]GTAATACCAGCACTT | 286053 |
rs186609889 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243908 | ATCTTTGTCACTGAA[A/G]GACTCACAACATATC | 286053 |
rs186614575 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205442 | TATTTGACATGCATT[A/T]TACTGTCCCTTATCC | 286053 |
rs186628474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191695 | AGTTGGTGTGTTATG[G/T]CAGAGAGGAGGAGGA | 286053 |
rs186640720 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167389 | TGCAAAGTCAAGGCC[C/T]GGCATGGTGGTTTAT | 286053 |
rs186651517 | snp | C/T | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129197 | GAAATGACAAGAAGG[C/T]CCGGGCCAGTGTCCT | 286053 |
rs186663116 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257337 | TGCCCACAAAAGAGA[C/T]GGGAAAAGAATGATC | 286053 |
rs186691531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196867 | CTCCAGCACCTGTTG[A/T]TTCCTGACTTTTTAA | 286053 |
rs186695322 | snp | A/G | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092130 | CCTGTCCGAGACGCC[A/G]TCTCTCCATCCTTTC | 286053 |
rs186705724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220587 | CTCTGCTTGACTTCA[C/T]TGAAAGTAATAAAAT | 286053 |
rs186706889 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163470 | ATCCATGTTCTACCA[A/G]GCTGTGACCTTGGAC | 286053 |
rs186722597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126643 | AGGGCATCATATTCT[A/G]TTGGCTAGGCAGAAT | 286053 |
rs186746159 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093123 | CTAGGTAGCTTATGA[A/G]CAACAGAAATTTATT | 286053 |
rs186752429 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111973 | GGAGTCTAGTTGAGT[C/T]GGGGAGATTTCTTTT | 286053 |
rs186761351 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154129 | AAATTGCGATACTTC[C/T]GTTACTATAATATTT | 286053 |
rs186763402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140135 | TTAGAATTTTTCAAC[C/T]GTATGCTTGATTACT | 286053 |
rs186779549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358213 | TGGCAGGTGCCTGTA[A/G]TCCCAGCTACTCGGG | 286053 |
rs186783452 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339130 | AGGAAGGGACACTGC[C/T]CTGCAGTGTCTTCTG | 286053 |
rs186790336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101007 | CATGCTAAAGGAAGT[A/G]CCTGGCACTTAAAGA | 286053 |
rs186791192 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277588 | CTCAGCTCACTGCAA[A/G]CTCCGCCTCCCAGGT | 286053 |
rs186797440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246495 | CCCCAAAAATGTTTC[C/T]TAAATGACCAAAATG | 286053 |
rs186830169 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217352 | TTATTTATTTATTTA[A/T]TTATTTATTTTTTAT | 286053 |
rs186849694 | snp | A/C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184380 | AATGGAGTTGGAAAA[A/C/G]GAAAGAAAATGTTTC | 286053 |
rs186865835 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149594 | TCCTAATCTATTAAA[A/T]TATGTTAGAGCTTGA | 286053 |
rs186870019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106663 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 286053 |
rs186874269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361767 | GTTGTTATCACTCCC[C/T]GTGCTGCTTAGTGAC | 286053 |
rs186913689 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345074 | ACAGCCGATTACTAC[G/T]GTACTTCTGTACTTT | 286053 |
rs186919096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111182 | AGTTTTCACTGTGTG[A/G]CAGTTACTTCAGAGT | 286053 |
rs186938434 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310023 | TCTACTATGATGGGG[A/G]GACCCTCATCCTAGG | 286053 |
rs186974040 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291974 | ATCTTGTGGTTCTGT[C/T]CTCCCGCACTCAATT | 286053 |
rs186978423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258956 | TGCCCAGGCTGTAGT[A/G]CAATGGCACGATCTC | 286053 |
rs186978798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275717 | TGTGTTTTCGATGCC[A/G]TATGAGGTGTTTTGC | 286053 |
rs186979077 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331724 | CTTCAGAACCCAAAT[A/C]CCCTGCAAGGAATGT | 286053 |
rs186982170 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135467 | TCTTTATCTAACCCA[A/C]GTTCCCAAAGATTTT | 286053 |
rs187021615 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338503 | AAGCATCTATTGCAT[C/G]AAAATTCCCAAGTGG | 286053 |
rs187021750 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318645 | ATAACAGGTACCACA[C/T]TGAACTTCCCTCCTA | 286053 |
rs187027544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103751 | GCAGTGTCTAATCTG[A/G]TAATTCCATTTAGTG | 286053 |
rs187036231 | snp | C/T | 5.07275e-05 | 0.00503599 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357828 | GGCCTAGTGAGTGGA[C/T]GCAGGGAAGGAAGTG | 286053 |
rs187038035 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283141 | CAATGATTAAATATG[A/G]CAACCTTCTATATAA | 286053 |
rs187047241 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266834 | GAAACTTAGACCTTC[A/G]AATTGTACTCCAGTG | 286053 |
rs187051297 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113349 | TAAAATGAGTCAGGT[A/G]TGGTGGCATGCACCT | 286053 |
rs187053082 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299704 | TTGGGAGGTTGGCAA[C/T]TCATTTCACTGAGAA | 286053 |
rs187065557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252457 | CGTGAACCCAGGAGG[C/T]GGAGCTCGCAGTGAG | 286053 |
rs187100501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356011 | CAGAGTGTCCATAAG[G/T]TCAAAACTGTCTTTA | 286053 |
rs187106060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246762 | CATCTTTATTGAGGT[A/G]TGATTGAAAAATAAA | 286053 |
rs187111280 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278194 | ATTTTGTTTTGTTTT[A/C]TTTTATTTATAAAAA | 286053 |
rs187113328 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262286 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGGTGCCT | 286053 |
rs187117132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227174 | CCTTGCCCATCCTCA[A/G]ATTGGGGGGCAGCCT | 286053 |
rs187121239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201766 | CTGCGAAAGTTTCTG[C/T]TGCCTTTTGTTCAGC | 286053 |
rs187121925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315936 | GCCTCCTGAGTAGCT[A/G]TGACCATAGGCACAC | 286053 |
rs187122750 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186267 | GTCACACTGTCATGG[C/T]AGGGTTGAGTGAGTG | 286053 |
rs187131016 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208654 | TGAGTGCCAGCGTAA[A/G]TGTTTCATACAATTA | 286053 |
rs187131742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168846 | ACAAACAGAAGATAT[A/G]TGGTAATAAGAATGA | 286053 |
rs187143462 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131858 | GAGGTGCCTTGCACA[A/G]GTAGGTGCACCCTGT | 286053 |
rs187151983 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257864 | TCAATGGATAAGTGC[A/G]TGGAAAGTAAGAAAA | 286053 |
rs187155064 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221853 | CAGTATTCAGAAAGT[C/T]TTGGATTTTGAAGCA | 286053 |
rs187157098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312384 | TAATCTCAGCACTTT[G/T]GGAGGCTGAGGCGAG | 286053 |
rs187160031 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281394 | GACTAAAATTTCAAC[A/G]CATTATACAGCAAGG | 286053 |
rs187164409 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353954 | TGTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 286053 |
rs187176358 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189413 | GAACAAAGAAGGAGA[A/G]GAAGTTGCTTATGAA | 286053 |
rs187179998 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115668 | AGGCAGGAGAATTGC[G/T]AGAACCAGGTGGGTG | 286053 |
rs187192368 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210274 | TGTTATGTGTTAGCT[A/G]TTCATTACTGTCATT | 286053 |
rs187206615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255004 | ATATGGCAGAAATGA[C/T]GCATTGTATCAGTTT | 286053 |
rs187208922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343505 | TTAGCCAGGCGTGTT[A/G]GCACGCACCTATAGT | 286053 |
rs187215957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195477 | AGCACATACATATAA[G/T]TCACTTAGTAATTAC | 286053 |
rs187220214 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178726 | ATACAAAAAATTAGC[C/T]GGGCATGGTGACGGG | 286053 |
rs187256114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205049 | AGCCCTTGGAATCCA[A/G]ACACTTAACATTCCT | 286053 |
rs187273714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303288 | CTGAATGGACACACC[C/G]TAAGTCAAGTTGTGT | 286053 |
rs187279117 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190076 | AATGTCACAACCAAG[A/G]TGGACTTTTTCAGGC | 286053 |
rs187280160 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172628 | AGGTTGCCTTATGTC[A/G]CTCTACAACTAGTGA | 286053 |
rs187291101 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154770 | GACAGTACACAGATA[C/T]ACACTTTTTTTTAAT | 286053 |
rs187300057 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135936 | CTTGTCAATTTCTAC[A/G]GAGAAGTCGGCCAAG | 286053 |
rs187307049 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120054 | TTAAACAAATATGTC[C/T]AAAATATTTTAACAT | 286053 |
rs187317407 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246252 | GCAATGTCGCAATCT[C/T]GGCTCACTGCAACCT | 286053 |
rs187336241 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336388 | AGGTGGTCATTTTCC[C/T]GAGATCAAATAGCTA | 286053 |
rs187338739 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243184 | ATATACAATTGTAAT[A/T]GAGAATACATTCAAT | 286053 |
rs187353135 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207096 | CATATTCAAAAATTC[A/G]AAAACTAAGTTCCAT | 286053 |
rs187356773 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297148 | CACACCCATTTTTAA[C/T]AACCTGTATTTCATA | 286053 |
rs187360014 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264594 | GTATTTTTAGTAGAG[A/T]TGGGGTGTTTCACCA | 286053 |
rs187364279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174696 | TTTTTCCGAAAGGCT[C/T]GAAGGAGGAAAGGTG | 286053 |
rs187373497 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204405 | CCGAGAGGACACTAT[A/C]CTGTGACTTCACTTC | 286053 |
rs187384626 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171917 | CAGAGAGAGCTCTTG[A/T]GCACTTGGCAGTGTG | 286053 |
rs187429760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360096 | CGAGGGGTGGCTGAC[A/G]TTTCTCATCTGGGTG | 286053 |
rs187456777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173006 | TCCATTATCTTTCAC[C/T]GCTAGATGTGGTCAA | 286053 |
rs187456852 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231785 | TTAACTGTAGCATGG[A/G]TGACATCATCAGGTA | 286053 |
rs187457600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284482 | AGGTTCTATCCTTAT[C/T]GAGGATTGTTCAACT | 286053 |
rs187469440 | snp | A/C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322864 | CATCAAAAATATGAA[A/C/T]TACTGCCAACATGGC | 286053 |
rs187473647 | snp | A/C/T | 0.0107367 | 0.0726029 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197415 | TCAGCTTTCTACATA[A/C/T]GACTAGCCAGTTTTC | 286053 |
rs187478760 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136189 | AAGTATTATGGCAGG[G/T]TTTTGATAAACAGGA | 286053 |
rs187493163 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103396 | CAGAGGAGCAGCATG[A/G]TCCTTTTGTTTTGTT | 286053 |
rs187500301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119468 | ATTCTGCTTTTTTGT[A/C]TTTGGAGCTGAAGCT | 286053 |
rs187510140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323297 | TGTAGATATTGACGA[A/G]ATTATTCTGAAATTC | 286053 |
rs187518260 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343961 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACACCA | 286053 |
rs187519139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361116 | TTTTTTTTTGAGACA[A/G]AGTCTCACTCTGTCT | 286053 |
rs187521331 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286033 | CCCCGAGAACAGTCC[A/G]CTAGCAGCACTTGTT | 286053 |
rs187532176 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271468 | CAAGGATAAGTTTCG[A/G]CTTAAATACCTAGGT | 286053 |
rs187533354 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228872 | GTGGCCACTCACAGA[C/T]GGAAGTAGAAACTCA | 286053 |
rs187533584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303703 | ACAAAAATGGAGAGT[A/G]AAACAGAGAGGAAAT | 286053 |
rs187538422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247959 | ATGACAGTAAACAGA[C/T]AACTATTATAATAAG | 286053 |
rs187587302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260583 | TTGGATCTAGGTGGC[C/T]GTCTTCTTTGTGGTT | 286053 |
rs187596386 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225689 | TTTTATTTCTTGATA[C/T]ATTTTATAAGAAAAT | 286053 |
rs187602172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107257 | AGTGGCACGATCTTG[A/G]CTCACTGCAACCTCC | 286053 |
rs187602778 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123600 | TGTACATGCGCACAC[A/G]CACACAAACACACAC | 286053 |
rs187610583 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193522 | GCTTCTACCTTGTCT[C/T]TTTATCTACCTTCAT | 286053 |
rs187614001 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100576 | TTTTTATTTTTATTT[C/T]TTTGAGACCGCGTCT | 286053 |
rs187619817 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115101 | ACTTTGTACATTTTA[C/G]GTTCTCTTTAAATGC | 286053 |
rs187630088 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157946 | AATGCTTGATTAAAA[G/T]AATTTCCTTAAAGAC | 286053 |
rs187694010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252099 | CCTAGCTGAGATTGC[C/T]CAGGAGAGTATAGTC | 286053 |
rs187700945 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266254 | GTGCCACCACGCCCG[A/G]CTAATTTTGTGTTTT | 286053 |
rs187702381 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232795 | CTTTTTGGATATGTA[C/G]AAATACTTTTAATAT | 286053 |
rs187705775 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213134 | TTTGAAAGAGTCGAC[C/T]TGTATGAAAAAGAAA | 286053 |
rs187712834 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365419 | CTGCACCCTGCAGGA[G/T]CCCCCATGCTATTTT | 286053 |
rs187724574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155485 | AGTAACCTAAGATTG[A/G]TCAGTGATTCATTTA | 286053 |
rs187726147 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214019 | TAGAAGGTAGAATAA[A/C]ATCTGCTTTTAAGAA | 286053 |
rs187732685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181283 | TGTTTTAAAAAATGG[A/G]TGTGAAGAGCCTGTG | 286053 |
rs187734307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197974 | AATGGGAGTTCACTC[A/G]TGATTTGGGTCTCTG | 286053 |
rs187734626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181678 | AAAGCAGAAGTGACT[C/T]TGACCTGCTAGGGTG | 286053 |
rs187739120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120293 | TTTAAATCAATCATC[A/C]TGTAACATTTTAGAA | 286053 |
rs187740346 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164913 | GAATAATTGTTTTCT[A/T]CTTGCCAGGTTAGCC | 286053 |
rs187747391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146898 | ACTTAAAGTATAAAA[A/C]AAACAAAACAAAAAA | 286053 |
rs187754151 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352335 | ATACAAAATTAGCCG[A/G]GGTGGTGGTGCATGC | 286053 |
rs187757797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327823 | TGACTGTATTAGGTA[A/G]CTAATTACCATAGGG | 286053 |
rs187759331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365994 | GGGCACCAAGCTGGA[A/C]CGTCCTCAGCACTGC | 286053 |
rs187778632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292380 | GCCAACATGGTGAAA[C/T]CCCATCTCTACTAAA | 286053 |
rs187784981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329401 | ACAAAACCTGGAGAC[C/T]GCCATTGTTTTTTGA | 286053 |
rs187792964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310135 | TGTGTAACTGGCAGG[A/G]TGAAACATCAGAAAA | 286053 |
rs187847259 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107017 | AAAACAACAAAAAAA[A/C]ACTTTCATTTTACCA | 286053 |
rs187853317 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362293 | CTTCTCTTATCCTTT[C/G]TGCTTTAAAAACTTG | 286053 |
rs187864055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323719 | ATAAAACCTAAAACT[A/G]TAGAAGCCCTAGAAG | 286053 |
rs187871669 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159617 | AAGCAGTGCATGACT[A/C]TACAGGGTTTGGTAC | 286053 |
rs187878043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140860 | ATATGTTGCCTGGGA[A/G]ATGCTCTTGTGGCCT | 286053 |
rs187879946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168127 | AAAGATTTTATTTTT[C/T]TTTGTGGACTACTTA | 286053 |
rs187886000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123758 | TGAAATTCATTTCAG[C/T]AGATAATTAATTTAG | 286053 |
rs187903299 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287475 | TACACTGCTTGATTG[C/T]TCTCCTGGCTAGAGA | 286053 |
rs187906515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354992 | TAAAATTAGCTTCAG[G/T]CTATGTGTGTAAGCT | 286053 |
rs187917695 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256660 | GTTGGGTGCGGTGGC[A/T]CACGCCTGTAATCCC | 286053 |
rs187924238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294879 | TTGGTTAAATCCACA[A/G]TGTGATGTCACCCAG | 286053 |
rs187928555 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218609 | TAGACGTGGGGTTTC[G/T]CCATGTTGGCCAGGC | 286053 |
rs187932346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287633 | TCAGGCTACAAACCC[A/G]CTCAACCCTTTAAAA | 286053 |
rs187936465 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332819 | TTACCTCTTTAGTTG[A/T]CCCTGTGAGAAGCCG | 286053 |
rs187937613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313816 | TCTCTCAACAGACTT[G/T]GCAGAACAAAATGAA | 286053 |
rs187941506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271907 | GAGTTTATAGGTGGG[A/G]ATTATTGCTCCGTTT | 286053 |
rs187960895 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194382 | CTTCTTTCACTTATC[A/G]GAGTGCATTTGACAT | 286053 |
rs187970871 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158934 | AGTAGTCACTGGTTG[C/T]CTACAGTTTCACTTT | 286053 |
rs187997636 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351355 | ACATTTTGTGACATA[A/T]AAAAAAAAAAACATA | 286053 |
rs188012251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309742 | AAAAAAAATGTATTA[A/G]TTGTTCAAATTTCCA | 286053 |
rs188032595 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275385 | AAAAACTATCTTGCC[A/G]AGTGGGCTATGAACT | 286053 |
rs188058011 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243501 | AAAATAATAATTTTT[A/T]AAAAAAAAAAACCTC | 286053 |
rs188064279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215919 | GAGACCCTGTCTCTA[C/T]AAGAATTGTGTGTTG | 286053 |
rs188068506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182382 | CCTCATTCTAAGTTG[C/T]GTTTTATTGTTGTTG | 286053 |
rs188090132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148387 | CATCTCATTTATTTC[A/G]TTTTGCAGCTCTTTT | 286053 |
rs188107372 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183387 | CAGTAAGCATTTTCC[C/T]CATATTTTAAGTTTA | 286053 |
rs188114916 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165996 | TAAACTGATGGAGTA[C/T]TAATAATTTCATAAT | 286053 |
rs188117308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148899 | AATTACAAAACATCC[A/G]TTACATTAGGATGTA | 286053 |
rs188127435 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127566 | ACATGGAAGATGCAG[G/T]TTTTGTTAGTTGTCT | 286053 |
rs188140907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315370 | TGAGAGTGAAATGAG[G/T]TGCACTGTAGCACAG | 286053 |
rs188148506 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304585 | ATTGAGGCTGGGTGC[A/G]GTGGCTCACACCTGT | 286053 |
rs188149231 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336119 | AAGGAACCATTGATA[G/T]GGCTTTGAAGATAGG | 286053 |
rs188151699 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355863 | GTTTTTCAGTTGGGG[A/G]CCAATGGGATGTAAC | 286053 |
rs188185884 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271685 | AATCAGGTTTCATAG[A/G]CAGGAGCTCCTGGGG | 286053 |
rs188194510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240018 | CTGTTGAGGGTCAGG[A/G]TCTAAACAGAGATTC | 286053 |
rs188197902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238543 | TATCAAATAAGTGCA[C/T]TGTTAGCTGGGACTT | 286053 |
rs188200055 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200977 | GGTATTGAAGCTTGT[C/G]CATGCATCACGAAGT | 286053 |
rs188223209 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168650 | ATGGCACAAGTCCCA[C/T]TAATGAGGGCTTTGC | 286053 |
rs188242008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130950 | TGCTTCTGTGACAAA[A/C]AAGTTCATCAGCTAG | 286053 |
rs188245581 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176419 | TAAACTCTTCTAGCC[G/T]CCCTTAAAATGTGAT | 286053 |
rs188252954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330395 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 286053 |
rs188283329 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276653 | GAACCTTTGAATAAA[C/G]AAGGAAGGAGAAAGG | 286053 |
rs188292775 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327127 | AAAAAATTAGCCGGC[G/T]TGGTGGCGAGCACTT | 286053 |
rs188293641 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311415 | TCTTATTTTTACCTT[A/G]GACTTTCAAAAACAT | 286053 |
rs188298728 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293799 | TTCTTTATAACAGTT[G/T]TATTAAGATGTAATA | 286053 |
rs188304623 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245870 | GTCTCTACTAAAAAT[A/G]CAACAACTAACTAGG | 286053 |
rs188310095 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260509 | TGGCTCCCTCACTTA[G/T]TGGACGTTGAACCTT | 286053 |
rs188314593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225164 | GAGTTTGAGAACTTA[A/G]TGTTTTTACATATTA | 286053 |
rs188326824 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258457 | TATCCCATTCACCCC[C/T]GCTCCCCCCACCCCA | 286053 |
rs188328548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289995 | TAGTGTTTTTCACGG[A/G]GTTTAAAGAATGTTG | 286053 |
rs188336691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233929 | TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA | 286053 |
rs188339058 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198266 | GCCTTATCTTGTGCC[A/G]GTTTTCAAAGGGAAT | 286053 |
rs188356019 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222244 | TTTTTTAAAATTTTT[A/T]AATTGAGAAATAATA | 286053 |
rs188361005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094039 | AAACTCCTGGCCTCA[A/G]GCAATCTTCCTGCCT | 286053 |
rs188365943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165688 | CTTCAGAAGTATTCT[A/G]TATGTTAGGAAGCAT | 286053 |
rs188382157 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127363 | TGTGTGTTTCTGTGT[G/T]GGGGGAGATTGTCTT | 286053 |
rs188401686 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335303 | AGCCCCATGTTTAGC[A/G]TTTTACATAAAATGC | 286053 |
rs188407997 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315017 | AAAGGAAGGAGATAT[A/T]ATTAGGCACAAAGAA | 286053 |
rs188423033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095550 | AGCGAGCATGATCAT[A/G]TCACTGCACTCCAGC | 286053 |
rs188428547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280946 | TGCTGCCCTACAAAC[C/G]TACAGTCTTCCTGAA | 286053 |
rs188444516 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296261 | TCACTTCTGCTGGGT[A/G]CATGACATATTGAAT | 286053 |
rs188450133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248520 | TAGCTGGGCATGGTG[A/G]TGCATGCCTGTAGTC | 286053 |
rs188454305 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202698 | TTATTAGAGGCATTT[A/T]CTTTAATAATTTTCA | 286053 |
rs188458691 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221048 | GATACCAGTCCTGCA[A/G]TAGCATTCCCCATAT | 286053 |
rs188458709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264114 | AAGTGTAATCCAGGT[C/T]CATGAGGGAGTCTCT | 286053 |
rs188469557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229162 | CAAGATAGAAGACCA[A/C]AACAGAAGTCCAAGC | 286053 |
rs188469750 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188231 | CTATTTTTAGTTGGT[A/G]GCTTTTCCGTCTCCT | 286053 |
rs188471883 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171066 | TTACTGTGACTCCAA[C/G]TATATGGCTCACCCC | 286053 |
rs188480839 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218526 | AAGCAATTCTCATGC[C/T]TCAGCCTCCCGAGTA | 286053 |
rs188487898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153910 | GCTCACTTTATTTCA[A/G]GGTATTTTTTTGGCT | 286053 |
rs188503698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185719 | AAAATATTAACATAT[C/G]AAAAATAAGCCTATT | 286053 |
rs188511890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334319 | AGCACAGCGCTCCAG[A/G]CTGTGCTAAGTGAGT | 286053 |
rs188520011 | snp | A/T | 1.66482e-05 | 0.0028851 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151159 | AATAATTGCAATTTT[A/T]TTTTCTTTCAGCTGA | 286053 |
rs188528591 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295813 | TTTCTTTCTTTGTTT[G/T]TTAAGCTCTAATGAA | 286053 |
rs188544001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094438 | TTGCTTTTCAATTCA[A/G]TCTCAGTCTTAATCT | 286053 |
rs188556697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263420 | TCATGTTAATTTTAC[A/T]GCTGGATCCTAGGTT | 286053 |
rs188589260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245566 | TAAGCTCGATAGCAT[A/C]AACATAAGTGAGTTA | 286053 |
rs188599275 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206258 | AGATCATATGTATAT[A/G]GGAGAAAAGATTACA | 286053 |
rs188601791 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224992 | GTTTTGTAGGACATT[A/C]GATTTTTTCAAATTA | 286053 |
rs188607679 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192650 | ATAATACTAATGACT[G/T]GCTACATTTCATTTC | 286053 |
rs188622467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114596 | TGGAGACATTTCTGG[C/G]TGTCACAACTCGGGG | 286053 |
rs188624193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174180 | GTTTGCAATAATCTG[C/G]TTGATTATTTGAATA | 286053 |
rs188630175 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157458 | TGACTTTAGGTATTC[A/G]CTCTTCAGACACTTG | 286053 |
rs188639785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137418 | TTCGTATCTTTTTCT[C/T]GGTATAAATGTGTTT | 286053 |
rs188646186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121715 | CCAACTTGTGATGCT[G/T]TTTGTGTACCTGGCA | 286053 |
rs188667947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357432 | TTAAGGAGGGAGTAA[A/T]GAAAAGTGCTGGGGG | 286053 |
rs188680814 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269601 | TGAATGTGAACATTC[A/G]ATGATCATAGCTTTC | 286053 |
rs188683087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282705 | CCCGTTGTCTGTGTA[A/T]AATATACTGTGCTTG | 286053 |
rs188690915 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284060 | TTGGGAGGCTTAGGC[A/G]GGAGAATGGCGTGAA | 286053 |
rs188695344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317978 | ATGTGATAGAGGATT[A/G]ATTTCCTGCACAAAA | 286053 |
rs188699643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259962 | TGTAATCCAACCTCT[C/T]CTCTTATAGATGAAG | 286053 |
rs188710005 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223765 | ATTTCTTGGCCACTT[A/G]TGTGTCTTTCTTTTG | 286053 |
rs188771478 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133450 | AGTAATAGTTTGTCT[C/T]TAAATTCAGCCGGGT | 286053 |
rs188780346 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159922 | CCATGATGGCGCCAC[C/T]GCACTCCAGTCTGGG | 286053 |
rs188782947 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307153 | TTGTGGGTACCGGTC[C/T]CTGGTAGATTTAGTG | 286053 |
rs188792042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345814 | AGAGTAGGAGATGAG[C/G]ATACTTACTCTGGGC | 286053 |
rs188801502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355121 | AACACTTCTGGTCCC[A/T]AGCATTTCGGATAAG | 286053 |
rs188817750 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280805 | ATGGAGGAAATATTT[C/T]TATCACATAAGATTC | 286053 |
rs188821430 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314511 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACTTCG | 286053 |
rs188840130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279328 | ATAGCATGAACATTA[A/C]ATTTTCCATGCCACT | 286053 |
rs188842005 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247212 | GTATCGTGTACCTGT[A/T]GTCCCAGCTACTCAG | 286053 |
rs188857929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209242 | ATTGATTGAAAAAAA[A/G]TAGAAACAAATAATG | 286053 |
rs188874999 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178645 | GGAGGTGGAGGCGGG[C/T]GGATCACGAGGTCAG | 286053 |
rs188890007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099926 | AGGGAATGATTCAGT[A/G]GAGAGGGAAAATTTA | 286053 |
rs188910694 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150661 | TACTAGGATTACAGA[C/G]GTTAGTCACCACGCC | 286053 |
rs188968028 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244868 | TATAGAGGAGCGACT[A/G]CTCAAAGCTTAAACT | 286053 |
rs188972017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275925 | CTGTTATGTCTTTAG[C/T]CCGACCTAAATTCCA | 286053 |
rs188977573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299277 | TTGTCAGTGTGCTCC[A/G]TTTTTAAAAAGAAAG | 286053 |
rs188983518 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198782 | AGCTCCTCTTTGTAC[C/T]TCTGGTAGAATTAGG | 286053 |
rs188987302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137829 | CCTGTATTTTCTTTC[A/G]TAAGATGGTAATAAT | 286053 |
rs189030659 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342025 | TGCCTCAGGTGGTGG[G/T]GGGGTTAAGGGGAGA | 286053 |
rs189030973 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359140 | GGCGTGGTGGCAGGC[A/G]CCTACAGTCCCAGCT | 286053 |
rs189053293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302245 | TACAGGCATGAGCCA[C/G]CACGCCAGGTCCCAA | 286053 |
rs189071782 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321640 | ATGCAAAAATTCTAA[A/G]TAACTTTTTAGCAAA | 286053 |
rs189074270 | snp | C/T | 0.128976 | 0.218754 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324667 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 286053 |
rs189087751 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102706 | TCCATGAGAAACTGC[A/G]CTAGAAATGTATGGG | 286053 |
rs189097391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117981 | TAATTTTTAAAGACC[A/G]CATTCAATTTTTGTG | 286053 |
rs189106541 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263101 | ATTTAGAAAATATTA[C/T]TCAATTTACACATTG | 286053 |
rs189142767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227806 | CATAATAACATTTTG[C/T]GGTTTCTTTTAGTCT | 286053 |
rs189153146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195280 | TGTGTCTGGTAAGTC[C/T]ACAGGCATTTTTTTT | 286053 |
rs189163939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331429 | AGGGCCCTCCCTCAT[A/G]GGGTGCTTGTGAACA | 286053 |
rs189164114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311542 | AGCCATGCTTTATTC[A/G]TGGTATGTTGTGCAA | 286053 |
rs189169890 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353880 | AAGGGCAAGACTCCG[C/T]CTCAAAAACTAAAAA | 286053 |
rs189177180 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346086 | CGCTTGAAGCCAGGA[A/G]GCAAAGGTTGCAGTG | 286053 |
rs189195400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308052 | TGACTGGGTAACAGT[A/G]GCTCCCTGGTACCCA | 286053 |
rs189201214 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130774 | CACCATTATCTTCAA[C/T]GCTAATCTAGTGCTG | 286053 |
rs189204084 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288712 | GTCTTTCTTAACACT[C/T]GAGATACTGTGTACC | 286053 |
rs189209423 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324969 | AGCCTGAAAGTGCAG[A/C]GGATAGGGATTACTA | 286053 |
rs189239219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272754 | ACATATATATACACA[C/T]GTATATATATATACA | 286053 |
rs189281820 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122386 | CGAAAAATGGTAGTT[A/G]TTACCTTCTACAACT | 286053 |
rs189292186 | snp | C/T | 0.00517822 | 0.0506191 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367463 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 286053 |
rs189298891 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136759 | TAGGTTTAGGTGTTT[A/G]TGAATTATTACTATT | 286053 |
rs189307707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121054 | AAAAGAACTTGGAAG[C/G]CATCTTTTATTAACT | 286053 |
rs189333694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104172 | ATTTTGTAATTTTAG[G/T]AGAGACGGAGTTTCT | 286053 |
rs189340989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106053 | GTGTGTGCATACACA[C/T]ACACACACACACACA | 286053 |
rs189341129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267173 | CTGCCACGCCCGGTT[A/G]ATTTTTGTATTTTTA | 286053 |
rs189351961 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234236 | TTCCAGGTCCTTGAC[C/T]AGGCTATAAGTTCTG | 286053 |
rs189355920 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253208 | TATACACTTAAGGGA[C/G]CTACCTGTTCCCTTC | 286053 |
rs189360061 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091757 | TCAGACCCCGACTTC[A/C]GCCCCTGACTCCCCA | 286053 |
rs189360545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206540 | CAAGAAGTGTTGTAG[A/G]AGTAGTATCTATAGG | 286053 |
rs189361874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283880 | TCAAGTAGGCCGGGC[A/G]CAGTGGCTCACGCCT | 286053 |
rs189366642 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269174 | CTCACTTCAACCTCC[A/T]CCTCCTGGGTTCCAG | 286053 |
rs189367514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174647 | CTAGACAAATAACAT[A/T]CTTACCCATGTTTAA | 286053 |
rs189368393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110729 | TCAAATGACATTTAG[C/T]GACGTTTTGCTTAGA | 286053 |
rs189372536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235059 | GAGACCAGCCTGGCC[A/G]ACATGGTGAAAACCC | 286053 |
rs189386718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199681 | GAGAGTTTTGTAGAT[A/G]TCTATTAGGTCTGCT | 286053 |
rs189388780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216683 | GCAAATGCACAATGT[C/G]ATGTGTCCACTATAC | 286053 |
rs189406350 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166558 | AGGTGTGAGCCACCG[C/T]GCCTGGCCCTAAATA | 286053 |
rs189411944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363511 | GTCAAAAAAAGAAAG[A/G]GGAAAGAGGAGAGAA | 286053 |
rs189426386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289095 | ACACTTGGCCTTTTC[C/T]CCCAGTCTTTAATTC | 286053 |
rs189429518 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125363942 | AGGGCACTTTTTTTT[G/T]GTTTGTTTTGTTTTG | 286053 |
rs189434639 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355367 | AAGGGAAAGGAGAAG[A/G]AAGGAGAAAGGACTA | 286053 |
rs189436755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325979 | ATAAATAAAAATACC[C/T]GGGCGCGGTGGCTCA | 286053 |
rs189448816 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257503 | TAACTTTTGCCAAGC[C/T]GGACAAAACCAAATT | 286053 |
rs189503770 | snp | A/G | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196081 | AGACTGGGTTTCACC[A/G]TGTTGGCCAGGCTCC | 286053 |
rs189506914 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256829 | ACTAGGGGAGGCTGA[C/G]GCAGGCGAATTGCTT | 286053 |
rs189521003 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160608 | TTCCCTGATAGTCAC[C/T]CTCCCTATGTCTATA | 286053 |
rs189522318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240615 | TTCCTGCAGCCCTTT[A/G]ACTCTTCTTATTTTT | 286053 |
rs189529871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202018 | GCATGGGACCTGCCA[A/G]GCCAGGCACAGGAGA | 286053 |
rs189531853 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179540 | TGAGTTGAATGTTTT[A/T]AAATTTCATTTTGAT | 286053 |
rs189534275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218815 | AATAAACTTGACACT[A/G]ATGAACCATACATTT | 286053 |
rs189534292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161147 | GCCCAGTGAACTGTC[C/G]TTGGGAGAATGGAGA | 286053 |
rs189540036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187501 | CTTAAACTGCCTTCA[A/G]TATTACAGCTCATGG | 286053 |
rs189541477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124975 | ATGTTTTATATTTTT[A/G]GTAGAGATGGGGTTT | 286053 |
rs189547804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143441 | GCCTTTTCTTCCTTC[C/T]TCCTTGCCAAAATGG | 286053 |
rs189554153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125537 | GCAGGAAACAGTGAA[A/G]GCACCATGGAGTTAG | 286053 |
rs189578474 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353690 | GAGTTCGAGACCAGC[A/G]TGGCCAACATGGCGA | 286053 |
rs189583630 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276189 | CACCCCAGCCCCTGT[A/G]CTGCCCAGGGCCAGC | 286053 |
rs189584153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320346 | GGCAGGCTGAAAATT[C/T]TCCAAATTTCATGAA | 286053 |
rs189592042 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253835 | AAGAAAAAGTTTATT[C/T]CTTTGGGGAAAATTA | 286053 |
rs189594494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310846 | CATGTAACGATTAAT[A/G]AGATATGTTTATTAA | 286053 |
rs189603082 | snp | A/T | 0.0019984 | 0.0315469 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217355 | TTTATTTATTTATTT[A/T]TTTATTTTTTATTTA | 286053 |
rs189629306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283488 | TCATGCCACTGCACA[C/T]CAGTCTGGGCAAGTG | 286053 |
rs189642525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252965 | TACCTATAGAACACA[G/T]ATTAAAAGTCTCTAT | 286053 |
rs189646667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216357 | ATCAAATGATCTGTG[A/G]GTCCGGGCGCGATGG | 286053 |
rs189648722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193458 | AAACATATGAAAAAT[A/T]TTTTTTAAACCACAT | 286053 |
rs189681589 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347279 | GGCCTCTTTCCAGAG[C/G]CCATGTTCCTAAATA | 286053 |
rs189698530 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273672 | ACTACACTATGATAA[C/T]GATTCACTGGATTAT | 286053 |
rs189702944 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309414 | TTGCCATCATTGAGT[C/T]ACTTTACCATAGAAG | 286053 |
rs189721038 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308865 | GAAGATAGATGAAGA[A/C]GTGCATTTTCCTTAC | 286053 |
rs189733642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105064 | TTGCGCAGGGAGGAG[A/G]CCATTGCAAGACTTT | 286053 |
rs189735942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272934 | AGAGAACTGACTTGG[A/G]AGCTAGGCCAGGGTT | 286053 |
rs189738056 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241374 | TCAAATATACAATTA[A/T]AATACAGAATACATT | 286053 |
rs189778545 | snp | C/G | 1.66302e-05 | 0.00288355 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357205 | AGGCTTATCAACTCT[C/G]CATTTTCCTCTAGGT | 286053 |
rs189779519 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210744 | TTTGAGACAGGGTCT[C/T]ACTCTGTTGCCAAGG | 286053 |
rs189795800 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178923 | AGTAAGTGGGCCTTA[A/C]TCCAATATGACTGAT | 286053 |
rs189802667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170340 | AATTTTTTCACAGCC[C/T]ATATCCAGTCCATCA | 286053 |
rs189807783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142802 | AGAGACGGTTTCTCC[A/G]TGTTGGTCAGGCTGG | 286053 |
rs189849834 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293240 | TCTCAGGGATCTTGT[C/G]CATTAATCCACACTG | 286053 |
rs189864166 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108449 | AGCACTTAAGTGCAC[A/G]CTTGCTATTGGGTCC | 286053 |
rs189872053 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260439 | GGCTATATCTCTATA[C/T]TTTCGTGTGTGGTAG | 286053 |
rs189872564 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217656 | CAGGCGTGAGCCACC[A/G]CGCCTGGCCCTGATC | 286053 |
rs189880601 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235734 | TATTCATACACATCT[C/T]ATCTTCCTTTGGAAA | 286053 |
rs189882632 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199884 | GTGCATATATATTTA[G/T]AATGGTTAGCTCTTC | 286053 |
rs189883466 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200116 | CATTGTTGGGACTTG[A/T]CTCTTTATCCAATTT | 286053 |
rs189883483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185278 | GTTCTCAAAGTTTTT[A/G]GTCTTCTGCTCCCAT | 286053 |
rs189893637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098507 | TGTGTTGAGAATAGG[A/G]TGGAAGAGGCAAGAC | 286053 |
rs189896455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167819 | AAATGCAAGCATTGG[A/G]GGAAGTTTTCTCAGT | 286053 |
rs189898151 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354162 | GTCTCGAACTCCTGA[A/C]CTCAGGTGATCTGCC | 286053 |
rs189902757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114338 | CCGCTGCTATTGCCT[A/G]TAGGTACATGATACA | 286053 |
rs189904686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150193 | CTTCGGTCCCAGGCA[A/G]CAGGGAGAGATTACT | 286053 |
rs189909686 | snp | A/G | 0.000372648 | 0.013645 | intron-variant, missense | NSMCE2 | GRCh38.p7 | 8:125130290 | GCAAGTCATCAACAT[A/G]ACCAGTAATGTCAAC | 286053 |
rs189925124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313509 | TCCAAATTTGTATTT[C/G]ATGACAGACAGGCCT | 286053 |
rs189929184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294654 | ATTGACTTTCTAAAA[C/T]AAAACCATAGTTCTT | 286053 |
rs189937827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332210 | ATTTTGCCAGTCACC[A/G]ATGCTAAGTCAAAAT | 286053 |
rs189939674 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359634 | CATCGCGCCCAGCCA[C/T]GGCATGCTTTCATTA | 286053 |
rs189960752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246912 | TTTTTCTCTTGTGTG[G/T]TTAAAATACTTAAGA | 286053 |
rs189964965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279094 | CTCCAAAAGTTTAGA[A/G]TTGCCAGTTAAATAC | 286053 |
rs189966025 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352460 | TAGCCTGGGCGACAA[A/G]AGTGAAAATCCATCT | 286053 |
rs189970402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262449 | TAAATAAATAGTATA[A/C]AATTTTGTGAAAGTA | 286053 |
rs190014118 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097437 | TGTACCTGTATGCCA[G/T]GCAAAGGGAACTCAT | 286053 |
rs190022132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113537 | AGAACAACTTATGAG[A/G]AATACATTTCTGGGG | 286053 |
rs190049640 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187968 | ACATATAGAATATAT[A/G]GTATGGAGATAATTG | 286053 |
rs190054329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134440 | CACTTGCTACAGGCA[A/G]TCTTCTTACTTTTAG | 286053 |
rs190058897 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356520 | TTTTGGTAGAGATGG[G/T]GTTTCACCATGTTGG | 286053 |
rs190059458 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153733 | CTGTGTATTTCACAG[A/G]ATGATTATGTGAATC | 286053 |
rs190078901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297730 | GTCATAGCTAGTTGG[A/G]AGGCTGAGGTAGAAG | 286053 |
rs190087036 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337051 | AATTATGGGTTTGCA[G/T]GAATTGCAACTAATG | 286053 |
rs190091065 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316967 | GTTTTTCGTTTTTTT[C/T]TTAAGAGATGGGGTT | 286053 |
rs190095222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124210 | GTTCATCCATGTTGC[A/G]TGTATCAGTAAGTAC | 286053 |
rs190096477 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297427 | CTCATTCCATTTTCA[A/G]ATAGTTCTAAATGGG | 286053 |
rs190097734 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265393 | TGCCCGGCTGATTTT[A/G]TATTTTTTGAAGAGA | 286053 |
rs190104103 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243729 | GTGGAGTGAGGGAGG[C/T]GATAGTTATCTCAAA | 286053 |
rs190110217 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281982 | ACTCCTGCAGGGGCC[A/G]GGGAGGGAAGGAAAT | 286053 |
rs190110803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336520 | GAGTCAGAAGCTATG[A/G]GAGGATGATGAGGAT | 286053 |
rs190114196 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250874 | TTTACGCAGGAAGAT[A/T]TATGTTGACAGTTGA | 286053 |
rs190126904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108193 | TTTGATTGCTTATGA[A/G]TAGGAGGTAGATGAC | 286053 |
rs190148626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118576 | CCAGAACACTTCTTA[C/T]GAAGTAGCTATTGGC | 286053 |
rs190152660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241107 | ATCTGAAAATCTGAA[A/G]TCCAAAATGCTCCAA | 286053 |
rs190156956 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092912 | GGGTCAGGGTGAGGG[C/T]TGTCCTGTGTTTTGT | 286053 |
rs190163224 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111757 | GCGAGCCGAGATCAC[A/G]CCACTGCACTGCAAC | 286053 |
rs190185204 | snp | A/C/G | 0.00159649 | 0.0282165 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202298 | CCAGTCTTCTGCGTC[A/C/G]ATCACGCTGGGAGCT | 286053 |
rs190213783 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358694 | TGTGACTAGTTCTCA[A/G]TTGACTTCTGATAAC | 286053 |
rs190224668 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329974 | CTCTCCAGCCCCCTC[C/T]GAAAGAACCATCATT | 286053 |
rs190238895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366701 | CTTACTTAAACACTT[A/G]AGTATAAAAGAAGTT | 286053 |
rs190249505 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226563 | CTTGGGAAGCCAGCT[C/G]AGGCCTTGTGATCCA | 286053 |
rs190255758 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246659 | GTCCTATGTTATCTA[A/T]TCTATTTCAAAGCAT | 286053 |
rs190257711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208615 | GCTGTTGAATTAGAA[A/G]AAGAATAGGAGGAGA | 286053 |
rs190271438 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115997 | CCATAAGGCACACAC[A/C]CAAGTTGCAAATTGG | 286053 |
rs190272021 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193835 | TATCACTGAGACAGT[C/T]TGGTGGACAGTGAGA | 286053 |
rs190286329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176114 | TTTGAGCTAAAATGA[A/G]CAATTCGTTGAAGAG | 286053 |
rs190294281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158408 | AAGGAAATGTTTGAG[A/G]GGAAAAGAAGAGAGG | 286053 |
rs190298377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139797 | ATTTGTTTGCCCTTA[C/T]GTTGTCATTTTATAG | 286053 |
rs190317012 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356147 | CGCAGATATCCAAAT[A/C]CAACTGGCTGCTATG | 286053 |
rs190333113 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192118 | GAGTATGATGCCATC[C/T]ACACTCAGAAAGTAG | 286053 |
rs190342880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316127 | CTCATTCTTATCAAT[A/G]CATGATGATAACAGA | 286053 |
rs190345388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128077 | TGACTAAAATAGACA[C/T]GGCCATTGTGCTTTG | 286053 |
rs190355084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156458 | TTGGATTACAGCTAC[A/G]TATTTGTTTTTTTAA | 286053 |
rs190382690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281543 | CTCCCGGGTTCAACC[A/G]ATTCTCTTGCCTCAG | 286053 |
rs190386032 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281062 | CACCTTTTCTTTTTT[A/G]TCTACAACTTTTGTG | 286053 |
rs190407116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096141 | GCTTTACTAAGGTCC[C/T]TATGCTTGCCTGCAT | 286053 |
rs190407564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257263 | CACTCCAACCTAGGC[A/G]ACAGAGCAAGGCTCC | 286053 |
rs190412885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220020 | TTAAAGATTATATAA[C/T]GGGAAGTTCATTGGT | 286053 |
rs190419816 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249452 | TTCATGGGGAGTGTT[C/T]GGGACTCAAGTTTCA | 286053 |
rs190426311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323394 | ACTTATTCTACCTGA[C/T]TTCAAGACTTAATGA | 286053 |
rs190429780 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211156 | ATAACATTATTATAT[A/G]TGTATATTCTCTGCT | 286053 |
rs190445106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361270 | ACAGGGTTTCACCAT[A/G]TTGTCCAGGCTGGTC | 286053 |
rs190446783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119520 | AACAGGGTTTGAAAA[A/T]GACCATCACAGAAAA | 286053 |
rs190447062 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344108 | TACCCAAATTGAAAT[A/G]TTGCAGTTTTAAAGT | 286053 |
rs190463521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303725 | AGAGGAAATTTAAAT[A/G]GTACAGGTAATTTTG | 286053 |
rs190474933 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286279 | CTCTTCCAGATTTGC[A/C/G]CAATATTCAGAGACT | 286053 |
rs190483656 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153026 | CACGCCAGTGCACTC[C/T]AGCCTGGGCGACAGA | 286053 |
rs190493261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301462 | ATCGTACCTCACTAC[A/C]TGGAGGTGGCGGTGG | 286053 |
rs190500925 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341464 | TAGGAGTCAGGCCCG[C/T]AGGCTTTGAAAATGC | 286053 |
rs190513084 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101664 | TTACTAAGCTGAAAC[A/C]AATTGTGGTTGAAGA | 286053 |
rs190553160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364233 | ACAGGTGTGAGCCAC[C/T]GTGCCTGGCCATATT | 286053 |
rs190574515 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326898 | GAGGCAGAGGTTGCA[A/G]TGAGCTGAGATCTCG | 286053 |
rs190582342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205914 | ATAAAATGTGTGCCA[A/G]AACTCTTTAATATAT | 286053 |
rs190582760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309586 | AATAATTAGCCAGGC[A/G]TGGTGGCACATGCTT | 286053 |
rs190588279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149535 | GTTATCTTAAATTCA[A/G]AGTTTTTAGTTGAAA | 286053 |
rs190596464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350252 | ATAGAGAAAGTCTGT[A/G]TGGCTTCTTTAGCTT | 286053 |
rs190597509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173699 | TATGTGTCTTTTCAT[A/G]TGAAGACTGACAAGT | 286053 |
rs190615957 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289806 | ATTCAAATTCTGGTG[C/T]CTCCAGTTAGCAGTT | 286053 |
rs190652658 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264371 | TCATGCCTGTCACTC[G/T]CAGCAGCGCCTGTCC | 286053 |
rs190654516 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296813 | GGCTGGGCATTCCTG[C/T]AGGAAAATGGCCAAG | 286053 |
rs190668950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113170 | GTTTATTCATTCATT[G/T]TAGTGTTACCATTGT | 286053 |
rs190680830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229323 | TTACATTAGATTCGT[A/G]GTCTCAACTTTTTTT | 286053 |
rs190697785 | snp | C/G | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196359 | CCTCCCCCAGCACCC[C/G]TACTCCCTGACAAGC | 286053 |
rs190725959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284851 | CCCCTTTTCTGAGCT[C/T]ATGAAAAGAGAACCT | 286053 |
rs190728380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169581 | TACATTCCATCTCCA[A/G]ATTTTCCTGCTTCTC | 286053 |
rs190734165 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271107 | TCTACTAAAAAACAC[A/T]AAATTTTGCCAGGCA | 286053 |
rs190741826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282522 | TGCATCGCATATTTA[C/T]CTCTGCTCCACTTAC | 286053 |
rs190742223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303441 | TGAAGTTTGTGATGA[G/T]TATTGAAGGAACTAA | 286053 |
rs190742582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131964 | GAGTCTATGTTAACA[A/G]CATTGTAAAAGCTTT | 286053 |
rs190747794 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317332 | CCTCCGAATAGCTGG[G/T]ACTACAGGCACATGC | 286053 |
rs190748802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254558 | CCATTTTTTATATAA[C/T]TGACCCACATGGGTT | 286053 |
rs190751841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348647 | ATAAGTCTCATGAGA[G/T]CTGATGGTTTTATAA | 286053 |
rs190765138 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237400 | AAAGCTATTAATGTC[A/C]CTGTTACGGTTCCTA | 286053 |
rs190773399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200719 | GTTTGAATGTTGGCC[G/T]GCCTAGCTACGTTGG | 286053 |
rs190779274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218191 | TTAGAAACCTGTACT[A/G]AGAAAGCAGACTGAT | 286053 |
rs190780560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251655 | AATAGCAACCACTTA[C/T]TGGATGCCCGTTATG | 286053 |
rs190785069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230211 | ATCCAGATATCAGAT[A/G]TCTTTACAAAAGGCT | 286053 |
rs190795724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250435 | GGTTAGACTACCTCT[A/G]TTGATATATTGCTGT | 286053 |
rs190810440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211998 | ATTTACTTACATGTC[A/T]TAGTGCTCTGTAAAC | 286053 |
rs190816553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154422 | TCTCAGGTTACCTTC[C/T]GTTGTCTCTCAAGAA | 286053 |
rs190818889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180479 | GCATAGCAATTAAGC[A/G]AAAGAAGATTATGTC | 286053 |
rs190820966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135576 | TATGGAATAAGGTAC[A/G]AGGTATAGATCAAAG | 286053 |
rs190829041 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103489 | TGATATTGTTTGAGA[A/T]TTATGGATCTGTCAG | 286053 |
rs190832886 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163049 | TATCTGTATATAGCA[A/G]TGAAGAAAGAATGTT | 286053 |
rs190866756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342992 | GACTTTTTTTTTAAA[C/T]GAGTATATTGTGCCA | 286053 |
rs190899658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257785 | ATTATCCGCCCTCTT[C/T]GGCCTCCCAAAGTCC | 286053 |
rs190900855 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303194 | AGCTGCCTCCCTCTG[A/T]GAACCTGCAGTTCAG | 286053 |
rs190906886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221529 | GATTACAGGCATGAG[C/T]CACTGTGCCCAGCCA | 286053 |
rs190912288 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270115 | GAGAGAGGTAAAAAA[G/T]GAAGTTGGAGACAGT | 286053 |
rs190914741 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197809 | TTCACTATATTGATT[C/T]TTCCTATCCATGAGT | 286053 |
rs190914872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242196 | AGAAAGAGAGGAAAG[A/G]ATGGCTGAGGATTGA | 286053 |
rs190916469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235943 | TACATATAATGTTAA[C/T]GCAGGAAGAAATTGA | 286053 |
rs190917055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203553 | TTTAAGAACAGTTTT[A/G]AGTTCATAGCAAAAT | 286053 |
rs190921098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181453 | TTAATTGTGGCACCT[A/G]GGAAGTAGATGAATG | 286053 |
rs190923986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209123 | AATTTGATTTTCTAT[C/T]GTCAGCTATTTGTGT | 286053 |
rs190932107 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146662 | CAGAAAACCAAACAC[C/T]GCATGTTCTCACTCA | 286053 |
rs190941255 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126929 | TTTTATCTGTCAGTT[A/G]TTTTGTTTTGCTTAT | 286053 |
rs190957503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157954 | ATTAAAAGAATTTCC[C/T]TAAAGACTCCAAAGC | 286053 |
rs190966430 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337835 | GGGAGGTGGAGGTTG[C/T]GGTGAGCCAAGATCG | 286053 |
rs190971549 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138457 | TCTCGAACTTCTGGC[C/T]TGAAGTGATCCTCCT | 286053 |
rs190977404 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122948 | ATGTAAACAAATGGA[C/T]GTGATTTGAATAGTA | 286053 |
rs190983030 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298832 | TGATGGGTGACTTTT[C/T]AAATTAATCCTCTTA | 286053 |
rs190993397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326561 | TGGGATTGTGGAAAA[A/G]AGAGAGAGGACTTCT | 286053 |
rs191003041 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327310 | AACCAAAATTGGGAA[C/T]TATAATTGAAATATA | 286053 |
rs191010387 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265831 | TGTTTTTTAAATTTT[C/G]TCAGACTTGTAGGCC | 286053 |
rs191020586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231790 | TGTAGCATGGATGAC[A/C]TCATCAGGTAGTTAT | 286053 |
rs191021879 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258850 | TTGGTACAAGACATT[A/G]TGGTCACACAACTGA | 286053 |
rs191023611 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290256 | TTAAGTAGAAATGTC[G/T]TAGTCAAAACGTGAC | 286053 |
rs191067639 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231356 | ACAGTCTATTGTTCC[A/T]TTTTATTTGGCCAGT | 286053 |
rs191071097 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196888 | GACTTTTTAATGATC[A/G]CCATTCTAACTGGCA | 286053 |
rs191081855 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106436 | TGTAATCCCAGCACT[G/T]TGGGAGGCTGAGGCA | 286053 |
rs191097707 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163681 | ATCTGACAACCCATA[C/T]CTGAATGGCCACAAG | 286053 |
rs191111919 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126780 | AGGATAATATTGTAA[A/C]ATAGCAGTTAACATC | 286053 |
rs191137478 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284275 | GACAGAGTATGTCTT[C/T]GACTCTCACAAGTCC | 286053 |
rs191140687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322326 | TGAGTTATCATTGTG[C/T]CACTGCACTGCAGTC | 286053 |
rs191153879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227186 | TCAAATTGGGGGGCA[A/G]CCTCCAGATCCACAA | 286053 |
rs191171914 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194689 | CTTATAAGAAATGGA[C/T]ATTTTGTCGATATTA | 286053 |
rs191173640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254379 | ATGGTAGCTGTAAAC[A/G]GGACCCAATTTACAA | 286053 |
rs191218559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103033 | AGCACTTTGGGAGGC[C/T]GAGGCCGGCAGATCA | 286053 |
rs191235515 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309862 | GGCCTACACTGAGCT[A/G]GAGCATGATCTAATA | 286053 |
rs191243732 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351258 | GACACCTCCCATCCA[A/G]TTTTACATTGCTGGA | 286053 |
rs191247216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123498 | ATGAAAGAGCTAAAG[C/T]TCGAAGGGTTAAGTG | 286053 |
rs191251027 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275425 | AAGTGCCACTCTTTA[G/T]TCTTCCCTGTACCCT | 286053 |
rs191254263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149842 | TTATAGGTATGTAAG[A/G]TTTTTTTGTTTGTTT | 286053 |
rs191258673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115760 | TAAATAAATAAATCT[C/T]TCATGGCCATTAGTA | 286053 |
rs191307944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335787 | ATATGTCATTTATAG[A/T]AAGAGTTACTGATGA | 286053 |
rs191312408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315023 | AGGAGATATAATTAG[A/G]CACAAAGAATCACAT | 286053 |
rs191318291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212565 | GGTTCAGGTACGTGT[C/T]CAGTACCAAACCGTT | 286053 |
rs191324307 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180837 | AGTGGGTAGGTATAT[C/T]TGGAGCTAATAAGAT | 286053 |
rs191329012 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355555 | AAATACAAAAATTAG[C/T]CAGGCATGGTGTCGT | 286053 |
rs191333028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280997 | CCACAGAGGTTTTCA[G/T]GAAGAAAACTCTGCC | 286053 |
rs191335635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351748 | GGGCATGGTGGCTCA[C/T]ACCTGTAATCTCAGC | 286053 |
rs191342947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264189 | GAGTCTGAGGCATAG[C/T]CCAAAGTGGACTGTC | 286053 |
rs191348723 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145303 | ATGACAGCCCTGGCA[C/G]TGGCATACTTACAGA | 286053 |
rs191350720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106765 | CTTTAGGAAGCCGAG[A/G]CTGGAGGATCACCTG | 286053 |
rs191351315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296306 | TAAGAGAGAGAGAAT[A/G]TGCATGAATGAATGA | 286053 |
rs191358524 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310049 | CTAGGTAAACAGAGA[C/T]ACTGAAGCAAAATTA | 286053 |
rs191359194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365317 | CTCCACAGCCACTCC[A/G]TCGGCAAGTCCTATA | 286053 |
rs191363023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292116 | CCTACCTACAAGGAG[A/G]GCTGGACAAAGGTAT | 286053 |
rs191375517 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328187 | GATTCTTAAGTTATG[A/C]CATTGAAATTGACAG | 286053 |
rs191383422 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143951 | GAAAAGGACCTTGTG[G/T]CTGAGATCATAGGAA | 286053 |
rs191398283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275861 | ATTCAAACCCAGAAC[A/G]CTCCGCCTGCAAAAC | 286053 |
rs191400220 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258971 | GCAATGGCACGATCT[C/T]GGCTCACTGCAACCT | 286053 |
rs191402215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216467 | CAACATGGAGAAACC[C/T]GCTTTCTACTAAAAA | 286053 |
rs191404479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223185 | ACATGGTGAAATCCC[A/G]TCTGTACAAAAAATA | 286053 |
rs191411691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244180 | GAATGTTTCTCAACA[A/G]TTAGGCAGGAGGAAG | 286053 |
rs191478627 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283160 | CCTTCTATATAAAGC[A/T]CTTAGCACAAGGTCT | 286053 |
rs191479920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167391 | CAAAGTCAAGGCCCG[A/G]CATGGTGGTTTATGC | 286053 |
rs191494724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266844 | CCTTCAAATTGTACT[C/T]CAGTGTCTGTTAAAG | 286053 |
rs191494944 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299733 | AATAACCAAAGAACT[C/T]TTGGCTTATGGAAAG | 286053 |
rs191498975 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129659 | CTTATTTACATGCAA[A/G]TTAAAAATTGTTTAT | 286053 |
rs191530160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240049 | ACTGGACTGAACTGA[A/G]AAGACAACTAGATTA | 286053 |
rs191531265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312519 | AGTCCCAGGTACTTG[A/G]GAGGCTGAGGCAGGA | 286053 |
rs191543776 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201934 | CCACCCCATTCCCCC[A/G]CCTTCCTGCGAAGCT | 286053 |
rs191547667 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354057 | CTGCCTCAGCTTCCT[A/G]AGTAGCTCAGGTTAT | 286053 |
rs191549781 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218704 | GGTGTGAGCCACTGC[A/G]CCCGGCCAAAAGTTG | 286053 |
rs191559449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186981 | AATTTTATCCTTTAG[A/G]TACCCAGTGTCCTGT | 286053 |
rs191575656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151870 | AAGAAATGAGCAATA[C/T]GATTGCAGTCATGTT | 286053 |
rs191577947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277680 | CCTGGCTAATTTTTG[A/G]TATTTTGTATTTTTT | 286053 |
rs191583464 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131913 | TAAGTAAAAGTTCTT[A/T]AGTTCCAGAATTCAA | 286053 |
rs191639491 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126191 | AGTTCGAGACCAGCT[C/T]GGCCAACTTGGTGAA | 286053 |
rs191667323 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205240 | GTGCATGTCTACAAT[A/G]TGAGACCTTTAAAGA | 286053 |
rs191668836 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222851 | GTGGATTGCTTGAGC[A/T]CCGGAGTTCAAGACC | 286053 |
rs191681859 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190811 | TTAATGAATAACAGC[C/T]GACATTGTTTGAGTG | 286053 |
rs191684460 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127462 | TTAGTATGGGATTTC[A/G]TTTCAAGCAAAAAAA | 286053 |
rs191685747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172749 | AAATATGAATAGATA[C/T]TTTAGTCTTAGCTTT | 286053 |
rs191689240 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155467 | ATGTTTATAGAATAG[C/T]TGAGTAACCTAAGAT | 286053 |
rs191692464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160158 | TCTGGCTTTCATGCA[C/T]TCTAACTCTGAGCCT | 286053 |
rs191695270 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275054 | AGAATAATATCCTAG[G/T]TGGCTTCAGCACCTG | 286053 |
rs191696389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135944 | TTTCTACAGAGAAGT[A/C]GGCCAAGGTTTTGAT | 286053 |
rs191715532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243209 | TTCAATAATAGTGGA[C/T]GTATATATACTTAAG | 286053 |
rs191729103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100648 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAA | 286053 |
rs191737126 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115117 | GTTCTCTTTAAATGC[A/T]TTTTGAGTGAACCAG | 286053 |
rs191745565 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204521 | TTCCTTTATATGGAA[G/T]CATTAATTTTTCCCC | 286053 |
rs191757217 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172058 | TTAATACTCAAAGGT[C/T]AAGTAGATTATAGAT | 286053 |
rs191767583 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111262 | GACATTTACTGCCCT[C/T]ATGAATAACTGACCT | 286053 |
rs191792473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322973 | CTGAGGTGGGAGAAT[C/T]GCTTGAACCCAGGTT | 286053 |
rs191810720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360235 | CAGCAATACAGCCCC[A/G]TGGAAGTGTCCAGGA | 286053 |
rs191811836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331773 | TTCAAATTTCAGTCA[A/G]CGGTAAAGTTTCAGC | 286053 |
rs191817839 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131422 | AGAATTCACTCATAT[A/G]TAACAAAACTTCAGT | 286053 |
rs191834435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294399 | TTCCAAAAGGACTGC[A/G]CCATTTTACATTCCC | 286053 |
rs191847285 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260587 | ATCTAGGTGGCCGTC[C/G/T]TCTTTGTGGTTTAAT | 286053 |
rs191852780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095091 | CCTGGGCTCAAGCCA[A/G]CCTCCCACATTGGCC | 286053 |
rs191853786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294043 | GCTGTTTGGGACGTT[C/T]CATATAAACATGCAT | 286053 |
rs191860901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112248 | AAAGTAAAAGGCAAT[A/G]CCTACACCAGGATGT | 286053 |
rs191869248 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319013 | CTACCCAAGGCCAGG[A/G]AAAGAGCTATCTAAT | 286053 |
rs191874494 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338723 | CTGCAGGCAGCCTAC[C/G]CTTTCAAAATTCAGT | 286053 |
rs191879357 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225840 | GTACTGTTTGATGAG[G/T]TGTAAAATAACACGC | 286053 |
rs191885721 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168204 | GCTCATGAAGATTGT[A/G]GTGAATGGCAGCGAA | 286053 |
rs191890511 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193634 | TTTACTGAGAAAGAA[C/G/T]TATTGGTTAGGAGTG | 286053 |
rs191899876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130842 | AATTTCCCTCACCAA[C/T]ATTAAGAAACTGGAC | 286053 |
rs191903190 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119172 | TCACCTCCTGTTACC[A/G]TGGAATCTCACTCCA | 286053 |
rs191915518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104265 | AAAATCTTGGAATTA[C/T]AGGCATGAGCCTCCA | 286053 |
rs191940597 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357516 | TGCCCTGAAGGATCC[A/G/T]GGACTAAAGTCATGG | 286053 |
rs191967094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213161 | GAAATGTTGAACATT[G/T]GTACCCTTTTTTCTT | 286053 |
rs191996203 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189096 | AATGTTTTACTTTGT[C/T]ATAAGGTATAACTGT | 286053 |
rs192017119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100086 | GGGAAAGCAGAGTGT[A/G]TGAGAACTGATGCTG | 286053 |
rs192018829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258004 | TTATGACCCAAATAG[C/T]TCATGCCATTAAAGG | 286053 |
rs192022427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280814 | ATATTTTTATCACAT[A/G]AGATTCAAAGTTTGG | 286053 |
rs192031754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222207 | TAGGTATAAGGATGT[C/T]ATTGCCTTAAAGTAG | 286053 |
rs192041236 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189601 | TGCCTAGAAAAAGAG[A/G]GTCAGAACATAGTTA | 286053 |
rs192051721 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263736 | GCCTCCGTGACAGAG[C/T]GAGACTCCATCTCAA | 286053 |
rs192056378 | snp | A/G | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092241 | GGGAAGGTCGTTTGA[A/G]TAAACTCTCTGGACC | 286053 |
rs192064954 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228928 | TTACAAAGCTTATAA[A/G]AGACAGAACCAGTCC | 286053 |
rs192080696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210440 | CTCATCAATTTTTAT[G/T]TCCTCAGCAGCTTAT | 286053 |
rs192086108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195699 | TCTGGCACTGACCAT[C/G]AACCCACTTTACAGT | 286053 |
rs192090805 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178905 | TTAAGTTAAAATGAG[A/G]TCAGTAAGTGGGCCT | 286053 |
rs192092319 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343821 | TAATTCGGTGAAACC[A/C]CGTCTCCACTAAAAA | 286053 |
rs192139488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277108 | CCTTGAAGGAAGGAA[A/G]AGTGCTTTCTTCATC | 286053 |
rs192140490 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107022 | AACAAAAAAAAACTT[A/T]CATTTTACCATTAGC | 286053 |
rs192164261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246451 | CCTCCCAAAGTGCTA[A/G]GATTACAGGTGTGAG | 286053 |
rs192174952 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185552 | TTCAGGGGATCCACT[C/T]GCCTCAGCCTCCCAA | 286053 |
rs192175721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282839 | TGTGTAACACAGTGT[A/G]CAGCCCTACTGGGCA | 286053 |
rs192178455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207267 | AAAGAGTAAAGGTCA[C/T]ACCTGACTTCTCTTG | 286053 |
rs192180545 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352368 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 286053 |
rs192193572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366516 | CTGCACTCCAGACTC[C/T]GTCTCAGAAAAAAAA | 286053 |
rs192197904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150678 | TTAGTCACCACGCCC[A/G]GCTGCTATCTTTGAT | 286053 |
rs192199562 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103083 | CCAGCCTGGCCAATA[C/T]GGTGAAACCCCGTCT | 286053 |
rs192200787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252182 | TAAAGAGAAGCTAAT[A/G]TATGAGACTGGAAAG | 286053 |
rs192201357 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175188 | TTACCCTGTGCATGA[C/G/T]GAATTGGGTTGGTGG | 286053 |
rs192205743 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358267 | GAACCCAGGAGGCAG[A/G]GGTTGCAGTGAGCCG | 286053 |
rs192214145 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266659 | CTTACTCCTGAATAA[A/G]GTTCAGGCTTTCATG | 286053 |
rs192218242 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233323 | AACCATTTTTGTGAT[G/T]AATTTTTATTGATCT | 286053 |
rs192223678 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320493 | CAGCAACCAAAGGGG[A/G]AAAAGAAACATTATG | 286053 |
rs192228048 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173801 | TACTTGGAGGCACAA[A/G]CAAAGTAAAACATTT | 286053 |
rs192228458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329551 | TTTAGTTATAGACAA[C/T]CTCATTGCCAGCAGA | 286053 |
rs192228792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310255 | GAGTCAGACAGAAGG[A/G]AGTTCCATTCCCAGC | 286053 |
rs192230364 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198113 | GGGGTTTTCTAACTA[A/T]ACAATCATGTAATCT | 286053 |
rs192235249 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214560 | CTGCTTAGAATTTTT[A/T]AAAATTAATAGACTT | 286053 |
rs192237484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156545 | CTTAACTGGAGCAAG[C/T]AGGTGCTAGGTTGGT | 286053 |
rs192245718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136770 | GTTTATGAATTATTA[C/G]TATTTTTCAATAGGA | 286053 |
rs192245738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181805 | TCTGGTGAAGTTGCC[A/G]CATTTGTGATTTTCC | 286053 |
rs192255120 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121071 | ATCTTTTATTAACTC[A/T]TTTGGTTTTGTGTTT | 286053 |
rs192276490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252988 | GTCTCTATTTCTTAA[A/G]ATTGTTGTAAGGATT | 286053 |
rs192341947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171723 | CTATAATAATAATAA[C/T]AACAACAATGTGACC | 286053 |
rs192357155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288379 | GGTAGTGCATCATAC[A/G]CTGAAATAGAAAACC | 286053 |
rs192361690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134971 | GGAGTGCAGTGGCTC[A/C]ATATTGGCTTATTGC | 286053 |
rs192362437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257007 | GACATGTAGAAGTTA[A/G]TTAAAGGAGTCCGGG | 286053 |
rs192367734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114617 | CAACTCGGGGATGCG[G/T]GGAGCATGTGTGCCC | 286053 |
rs192368815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272074 | GCTGGAGTGCAATGG[C/T]GCTATCTCAGCTCAC | 286053 |
rs192371695 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195310 | TTAATGTTCTCCTGG[A/C]AATGCTAATGTACAA | 286053 |
rs192374304 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218844 | TTAAAAATGGTTAAG[A/G]TGTTAAATTTTATGT | 286053 |
rs192377626 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178667 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 286053 |
rs192380566 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159874 | CTGAGGCAGGAGAAT[C/G]GCTTGAACCCAGGAG | 286053 |
rs192383025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240762 | ATATTCCTGTCTAAT[C/G]AAGTAAACACCAACA | 286053 |
rs192383864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345526 | AACATGAAGCTGAAT[C/T]AGACAGTTCCTTCCC | 286053 |
rs192390821 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141499 | TTAGTGTCTGTGAGC[A/G]TCTGTTTCCTTATCT | 286053 |
rs192400579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123830 | GTTTTTTAAAAAAAT[C/T]CCTCTCAGTTAGTCA | 286053 |
rs192418310 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271696 | ATAGGCAGGAGCTCC[A/T]GGGGTTTCAACATCA | 286053 |
rs192425179 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093564 | TAAATAAATAAGTAA[A/G]TAAATAACATAATTG | 286053 |
rs192433734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112037 | TGAATAGAAGGAGTA[A/G]CTAGAAGTAGGTGGT | 286053 |
rs192482079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176984 | AAGGACAATTGACAT[A/G]CTTTCCCAGCTGGTT | 286053 |
rs192501136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140108 | AATTGGAGATACCAC[A/G]TGATTGTACTGTTAG | 286053 |
rs192541334 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101241 | TAATTAAAAAGGACT[A/T]ATAATGGAGAAACTA | 286053 |
rs192566940 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233961 | GCAGGCGGATCATGA[A/G]GTCAGGAGATCGAGA | 286053 |
rs192571584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198362 | TTTGAGATATGTTGC[A/G]TCGATACCTAGTTTA | 286053 |
rs192588632 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198627 | ACATCGATGTTCATC[A/G]GAGATATTGGTCTAA | 286053 |
rs192590420 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108054 | AAAAATAAAAAAAAT[A/T]ATGATGAAAATAGTT | 286053 |
rs192639338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365445 | ATTTTCCCTGCCCTT[C/G]TCTTACCTCCCTGTT | 286053 |
rs192642727 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300430 | AGCCTCCCAAAGTGC[A/G]GGGATTACAGACATG | 286053 |
rs192654504 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339230 | GGTCTCTCTCCTTGG[A/G]GGCTGGAGTGAGCTC | 286053 |
rs192672800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267577 | GATCACTTCAGCTCA[A/G]GAATTCAGGATCAAC | 286053 |
rs192675012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090039 | AGGGCACTTGTGTTT[C/T]CTATTTCTAATAATG | 286053 |
rs192678388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307752 | GACTAAGCAAGTGTC[A/G]TTTGCTCCCTGGAGG | 286053 |
rs192681600 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234281 | TCATCTAGACTAATA[G/T]CAGTTGAGAAGAAAT | 286053 |
rs192684297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355048 | TGTTTAGTCTTGGGT[C/T]CCATCCCCCAAGATA | 286053 |
rs192699526 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324799 | CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTGAT | 286053 |
rs192714550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205616 | AAAGTATCTTACTCC[A/G]TTTTCAGAATACCAA | 286053 |
rs192717193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185919 | GTCTATTTTGTTGAC[A/G]TACACAAAGAAAATT | 286053 |
rs192723278 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361848 | TATGACAGGAATCCC[A/T]CCCACTCAGATTTCC | 286053 |
rs192724397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124905 | GTTCAAGCAATTATC[C/T]TGCCTCAGCCTCCTG | 286053 |
rs192726856 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151496 | ATTAAATCTATTTTA[G/T]ATTGCTTGCAATTTT | 286053 |
rs192742698 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324367 | TACACAAATGTTCAT[A/T]GCAGCTTTATTTCTA | 286053 |
rs192743230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103757 | TCTAATCTGATAATT[C/T]CATTTAGTGAATTTA | 286053 |
rs192759296 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256749 | GCTAACATGGTGAAA[A/C]CCTGTCTCTATTAAA | 286053 |
rs192761417 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287537 | GACCTAAGTAAGACA[A/G]CTTTCTCCTCCAGGA | 286053 |
rs192770640 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282489 | AACAAAACCTATTTG[C/T]AGGCTACATATGGTT | 286053 |
rs192785031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330074 | TGACCTAGGAATGGG[A/T]GGGAACAGGTAGCTT | 286053 |
rs192790264 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367265 | CATGCCTGTAATCCC[A/G]GCACTTTGGGAAGCC | 286053 |
rs192796839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159271 | GGTATGTATGTATAG[A/G]ATAAAACATAGTCAT | 286053 |
rs192807140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123698 | CTATTAAGTTTGGAA[C/T]ATTAAGTAAAGAATC | 286053 |
rs192813754 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112178 | AATAGCATTATAACT[G/T]AAATTAGTGAAGATT | 286053 |
rs192830846 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252464 | CCAGGAGGCGGAGCT[C/T]GCAGTGAGCTGAGAT | 286053 |
rs192836616 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216232 | GTCAATGGACATTTG[C/T]GTTTTCACCTTTTGG | 286053 |
rs192845699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182522 | TGTCCCATTGCTGGG[G/T]AGGGAAATTGGGAAA | 286053 |
rs192854640 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148457 | CAGAAATTAACTCAT[A/T]TAATCCCAGAGGGAG | 286053 |
rs192862257 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355223 | TTCTATGGAACCGAA[A/G]GGTATGCCACACCAT | 286053 |
rs192871928 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120134 | AATTAGAATCTTACA[A/G]TACATGTCAACCTGG | 286053 |
rs192872665 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314637 | CTGAAAACAACCAAG[C/G]CAGGTGATGGTTGTC | 286053 |
rs192894551 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255562 | TGATCACAAGCAGAG[A/C]GGAAGGAAACAACAT | 286053 |
rs192896706 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218537 | ATGCCTCAGCCTCCC[A/G]AGTAGCTGTGATTAC | 286053 |
rs192896924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108221 | GACATGAGAAGTCCT[A/C]TGCAGAGAGAAAGCC | 286053 |
rs192918847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201461 | TTGGAGTTTGCTGGA[C/G]GTCCATTCCAGACCT | 286053 |
rs192919927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142558 | TATCATGTACTGCTG[A/G]CACTCTTCACTATGA | 286053 |
rs192922965 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168669 | TGAGGGCTTTGCCCT[C/G/T]GTGCTCTAATCTCTT | 286053 |
rs192929007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338338 | GGGAATATTTCTCAT[A/G]TAGTGAGATGAACAG | 286053 |
rs192948083 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275996 | TTCCTTTGATCTCAT[C/G]GCCTTCTGTGCCATC | 286053 |
rs192949177 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244990 | TTTAAGGGATTTTAA[A/G]CATTGAAATTGGCCA | 286053 |
rs192952318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299418 | AGGTAAAGAGCAAGC[A/C]AGGAATGTCTTACAT | 286053 |
rs192962504 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206048 | GGAAACAATCAAGAG[C/T]TTTGTGAAAATTATC | 286053 |
rs192984209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147776 | AACTCTGTGTTTCTG[G/T]GTTTATCCCTTTTTC | 286053 |
rs192989646 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352924 | TTGAGAGTCTTTCTC[C/T]TTTTAGACTCTTGGT | 286053 |
rs193005249 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295576 | TCTCTGCTTAGTACA[A/G]CTTTGGGAAGTTCTG | 286053 |
rs193016462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263133 | ATTAAATCAGCAAGT[A/G]ATGATTAAGTGCTCA | 286053 |
rs193017391 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094263 | TAACATCTTGCAAGA[C/T]AGTCACTAACAAAGT | 286053 |
rs193020958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202127 | CAGTCTGTCACGGCT[A/T]CCCTTGGCTAGGAAA | 286053 |
rs193030648 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228102 | TACTATGTATTGAGT[C/T]TTAACTATCAAAATT | 286053 |
rs193035464 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170008 | TCTTACAGCCTGCTC[A/T]GATATCATCCCATCT | 286053 |
rs193065278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334428 | GGGGATCCATGAACG[C/T]TGAATTCAGAGAGCC | 286053 |
rs193083677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295824 | GTTTTTTAAGCTCTA[A/G]TGAATTCTGTTTTGA | 286053 |
rs193098255 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191808 | TCTCGCGTAATCTTT[A/G]CAACATCCACACGCA | 286053 |
rs193099125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271625 | AATGAAATGGCTTTT[A/G]GCCCCTTAAAACTGA | 286053 |
rs193107557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120355 | GTAAAACGAGTTATT[A/G]TCTGTTGATTTCTTT | 286053 |
rs193122672 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239210 | GGTTAGGTTGCATCA[C/G]AACACTCAAAAGTCA | 286053 |
rs193140570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362456 | TCAGTGCAGCTGGCT[C/T]CTCTCCACGAGCTTC | 286053 |
rs193169294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292774 | AAAATAAGAGCAAAT[C/T]GATTCTGAAAAGTAG | 286053 |
rs193173382 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260292 | GTTAGCCCAGTATAA[A/G]AATGTGTTTTTCAGA | 286053 |
rs193177545 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318358 | TGGTAAGCCAAGATC[A/G]CGCCACTGCACTTCA | 286053 |
rs193182283 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224113 | AGTGCTGGGATTACA[A/G]GCATAAGCCACCATG | 286053 |
rs193185076 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192544 | ATAGGGAAAAAACTG[C/T]GTATAGAAATTCAGA | 286053 |
rs193192136 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165293 | TCAGAAAATATTAAT[G/T]GCCTCTTTTCATCTT | 286053 |
rs193197513 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127099 | TACTTCACTTCTTTA[A/G]CATTCTTTTCCATGC | 286053 |
rs193209985 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313926 | ATGCTTTCTTACTCT[A/G]TCTTCCAACCAAGAC | 286053 |
rs193213536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280598 | AAACCATCTGTTCAG[A/G]AATGATCCTATTAAT | 286053 |
rs193217457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209503 | AAATGTATTTTATTT[A/G]GTGCTAATTGAATAG | 286053 |
rs193242563 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104076 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 286053 |
rs193255180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173042 | CAGGTGTTCCAGGTT[C/G]CAGACACACACCTCC | 286053 |
rs193260165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136457 | GTCTAAGATGACTTT[A/G]TGTTTTAGGTCTTGC | 286053 |
rs193301218 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345880 | GCCATGGTCAGCCAG[C/G]CATGGTGGTTCATGC | 286053 |
rs199533258 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355959 | AGCAGTTCTCAAAGT[G/T]CAGGCCAGGGATCTC | 286053 |
rs199539617 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197367 | TCCATCTTGAATTAA[C/T]TTTTGTATAAGGTGT | 286053 |
rs199552694 | in-del | -/CG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143097 | CCCAGTGTGGGTGCA[-/CG]CACACACACACACAC | 286053 |
rs199554216 | in-del | -/TAAAAA | 0.0158469 | 0.0875917 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249936 | GGGAGGAATTAAAAA[-/TAAAAA]AGGAAAAAACATTGG | 286053 |
rs199556407 | in-del | -/TT | 0.00359137 | 0.0422231 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217355 | TTATTTATTTATTTA[-/TT]TTTATTTTTTATTTA | 286053 |
rs199557188 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202294 | ATCACCAGTCTTCTG[A/C/T]GTCGATCACGCTGGG | 286053 |
rs199566182 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119231 | GATTTTCTTTCCTCC[A/C]CCGACTGTAACAACC | 286053 |
rs199572839 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272846 | ATATACACACGTATA[C/T]ACACACACACATATA | 286053 |
rs199582077 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306371 | ATTAAAAAAAAAAAA[-/A]CTGAGCAACAGCTGT | 286053 |
rs199591334 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098789 | TGTAAAAGGAGTAGG[-/T]TTTGGGGGAGGGGTA | 286053 |
rs199604178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182061 | TTTGTTAACACTATT[A/G]TTATTAACATTTAAC | 286053 |
rs199627612 | snp | A/C/G | 0.000200066 | 0.00999986 | synonymous-codon, missense | NSMCE2 | GRCh38.p7 | 8:125182129 | ACGTCCAGAAAAAAT[A/C/G]CCAGATTTAAAATTA | 286053 |
rs199661331 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197555 | CTGTTCCATTGGTCT[A/G]TATATCTGTTTTGGT | 286053 |
rs199668487 | in-del | -/TGTGTG | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129545 | GAAAAGATTTGGCTC[-/TGTGTG]TGTGTGTGTGTGTGT | 286053 |
rs199691848 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201467 | TTTGCTGGAGGTCCA[C/T]TCCAGACCTTGTTTG | 286053 |
rs199703937 | in-del | -/G | 0.210624 | 0.24688 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356236 | TATGTCTGTGTGTAT[-/G]GGGGGGGGTGTTCTG | 286053 |
rs199711036 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265620 | TTTTGCCTCTCAGGC[A/G]GGTGGCCGCCTTACT | 286053 |
rs199715582 | in-del | -/TA | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194758 | TTTCAATGTGCAGTC[-/TA]TGAGAATTGCACCCT | 286053 |
rs199724639 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198629 | ATCGATGTTCATCAG[A/G]GATATTGGTCTAAAA | 286053 |
rs199726919 | snp | A/G | 0.00199792 | 0.0315431 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125151182 | TCAGCTGAAGTGAGT[A/G]GTGAATATAGTATGG | 286053 |
rs199756323 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315819 | TTTCCCTCTCTTTTT[C/T]AAAGTCAGGGTTTCA | 286053 |
rs199776687 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365303 | CCCTTTCGCTTATGC[C/T]CCACAGCCACTCCAT | 286053 |
rs199781466 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220644 | TAACATCATTATTTA[A/T]AAAAAAAAAAAAGTA | 286053 |
rs199857942 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197948 | ATTTTATTCTTTTTG[A/T]AGCAATTGTGAATGG | 286053 |
rs199866925 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313204 | AGAAAGAGAGAGAGA[A/G]AGAAAGAAAGAAAAG | 286053 |
rs199884509 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112976 | GTGTTTACATATTTC[-/A]AAACAAAATGTATAC | 286053 |
rs199899521 | in-del | -/ACGGGC | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178737 | TAGCCGGGCATGGTG[-/ACGGGC]ACCTGTAGTCCCAGC | 286053 |
rs199907072 | in-del | -/CTG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313800 | GAACTTTACTTTTCT[-/CTG]TCTCTCAACAGACTT | 286053 |
rs199918382 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198162 | GCTTCCTCTTTTCCT[A/T]ATTGAATACCCTTTA | 286053 |
rs199921947 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215288 | TGAGTGAGAATATGC[A/G]GTGTTTGGTTTTTTG | 286053 |
rs199926006 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272630 | TATAACCTTAACACT[-/C]TTATACTGCCACAAT | 286053 |
rs199928800 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111598 | TGAGGTCAGGAGTTC[A/C]AGATCAGCCTGGCCA | 286053 |
rs199941633 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199258 | GCTTCTCTAGTTCTT[C/T]TAATTGTGATGTTAG | 286053 |
rs199942523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171178 | CATTTCCACTCTGCT[C/G]AATTGTTCTCCATGG | 286053 |
rs199948891 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360047 | GTTAACGACATTTGA[C/T]GACTGACTGAATGTA | 286053 |
rs199994665 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316797 | TTCTTTCTTTCTTTC[-/T]TTCTTTCCTCTTGCT | 286053 |
rs200020413 | in-del | -/GAAA | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363621 | GGAGGGGGAGGGAAG[-/GAAA]GAAGGAAGGAAGAAG | 286053 |
rs200066843 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325515 | CCACCACACCTGGCT[-/A]ATTTTTTTTTATTTT | 286053 |
rs200069172 | snp | A/C | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367535 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAAGAA | 286053 |
rs200074935 | snp | A/G | 0.000280174 | 0.0118325 | missense | NSMCE2 | GRCh38.p7 | 8:125366799 | TGTAGCCACACGGAT[A/G]TAAGAAAGTCAGATC | 286053 |
rs200111566 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348485 | TGGTACCAGGGAGCA[C/T]TGGAACTTATATGGT | 286053 |
rs200138004 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199673 | TTGGGGTGGAGAGTT[C/T]TGTAGATGTCTATTA | 286053 |
rs200150664 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331129 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 286053 |
rs200167522 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196985 | CATGCGTCTGTTGGC[C/T]GCATAAATGTCTTCT | 286053 |
rs200173688 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262096 | GGTGAGACTCTGTCT[C/T]AAAATAAAATAAAAT | 286053 |
rs200177963 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217410 | GTGTCACCCAGGCTG[A/G]AGTGCAGTGGCATGA | 286053 |
rs200204667 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197775 | GAATCTATAAATTAC[C/T]TTGGGCAGTATGGCC | 286053 |
rs200212246 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353553 | CCAGAGACCCCACCC[C/T]ACAGCAAACATACTA | 286053 |
rs200213171 | snp | C/T | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125195949 | TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG | 286053 |
rs200227292 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243503 | AATAATAATTTTTTA[A/T]AAAAAAAAACCTCTA | 286053 |
rs200230252 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214826 | TGTTCGTGTATTAAC[A/G]TTTATATTACATAAA | 286053 |
rs200235110 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201421 | GTTTTCCTTCTAACA[A/G]TCAGGTCCCTCAGCT | 286053 |
rs200235977 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272014 | ATCTGCAGTTTCTTT[C/T]TTTTTTTTTTTTTTT | 286053 |
rs200237357 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240135 | TTTCTTTTTCTTTTT[-/C]TTTTTTTTGAGACGG | 286053 |
rs200254353 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200583 | TGTGGGTAACCTGAC[A/T]TTTCTCTCTGCCTGC | 286053 |
rs200258589 | in-del | -/TAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171710 | TAATAATAATAATAA[-/TAA]CAACAATGTGACCAT | 286053 |
rs200273856 | in-del | -/ACT | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116450 | ACCCAGCTTTCTGTG[-/ACT]TATTTTTACTAACTT | 286053 |
rs200290295 | in-del | -/AGTG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312996 | TGATGATCAAGAGAC[-/AGTG]AGTAGAGGATGGGTC | 286053 |
rs200291269 | in-del | -/AGTGGAT | 0.189576 | 0.242588 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216207 | CACATTTTGTTGATC[-/AGTGGAT]CACTTATCTGTCAAT | 286053 |
rs200342031 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272717 | ATATATATATATATA[A/T]TATATATATATACAC | 286053 |
rs200351174 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240130 | GCAGTTTTTCTTTTT[C/T]TTTTTTTTTTTTTGA | 286053 |
rs200393339 | snp | C/G/T | 0.000203723 | 0.0100907 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357832 | TAGTGAGTGGACGCA[C/G/T]GGAAGGAAGTGGAGC | 286053 |
rs200394797 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095921 | AGAAAATTGAATACT[-/G]GAATTATATCATTTG | 286053 |
rs200401815 | in-del | -/T | 0.140919 | 0.224948 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262695 | ACACTGGAAGTCTAG[-/T]TTTTTTTTTCTAAAA | 286053 |
rs200412773 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197616 | CCTTGTAGTATAGTT[C/T]GAAGTCAGGTAGCCC | 286053 |
rs200414551 | in-del | -/TA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353903 | ATATATATATATATA[-/TA]ATTTTATTGCTGTCA | 286053 |
rs200451724 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265159 | TCCTGGCTTTATTTA[A/T]TTTTTTTTTGGTAGT | 286053 |
rs200455082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338318 | CCTTTTATATAGAAG[C/T]TCTTGGGAATATTTC | 286053 |
rs200457945 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276909 | GCATTGCACAACTGT[-/G]GGGGGACACCATTCA | 286053 |
rs200479728 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199541 | TGCACTGTGGTCTGA[C/G]AGTTTGTTGTGATTT | 286053 |
rs200484132 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125151183 | CAGCTGAAGTGAGTA[A/G]TGAATATAGTATGGA | 286053 |
rs200486322 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197104 | GGATATTAGCCCTTT[A/G]TCAGATAGGTAGATT | 286053 |
rs200502032 | in-del | -/AGAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320185 | CATCTCAAAAAAAAA[-/AGAG]AGAGAGAGAGAAAGA | 286053 |
rs200524383 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349596 | TTTAAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA | 286053 |
rs200558318 | snp | A/G | 1.66482e-05 | 0.0028851 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125182147 | AGATTTAAAATTATT[A/G]GTAGAGAAGAAATTT | 286053 |
rs200597099 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271424 | ACTTGAATGGAAGAG[A/T]TAGGTGGAAATAAGA | 286053 |
rs200620788 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150398 | GATATCTTTGGTTTT[-/C]TTTTTTCTTTTTTTC | 286053 |
rs200624883 | in-del | -/TTG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340015 | AGTTTTTTTTTGTTT[-/TTG]TTTTTTTTTTTTTTT | 286053 |
rs200641269 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198695 | TATCAGGATGATGCT[A/G]GCCTCATAAAAGGAG | 286053 |
rs200662178 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284386 | CTTCAGAGAAGGAGG[A/G]ATTCTAGCGGAGTCA | 286053 |
rs200685886 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329935 | TAGTAAGACTGGTTG[A/T]TATTTTTTTTGTTAC | 286053 |
rs200689096 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310951 | ATGAATATATTAGAT[A/G]GCAAGGGGGAAAACC | 286053 |
rs200704328 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197458 | ATTAAATAGAGAATC[C/T]TTTCCCCATTTCTTG | 286053 |
rs200709156 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095431 | GTCGTCTCTACTAAA[A/G]ATTAAAAAAGAAAAA | 286053 |
rs200720623 | in-del | -/AAAAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312076 | AACTCCATCTCAATT[-/AAAAA]AAAAAAAAAAAAAGA | 286053 |
rs200723658 | in-del | -/A | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193087 | TATTTTGCAATCATT[-/A]AAAAATGATGTGAGG | 286053 |
rs200740750 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201476 | GGTCCATTCCAGACC[C/T]TGTTTGCCTGGGTAT | 286053 |
rs200782488 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282288 | CCAGCAAATTTTTGT[A/G]TTTTTAGTAGAGCCG | 286053 |
rs200782855 | in-del | -/GAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304965 | GGAAGGAAGAAAGAA[-/GAA]AGAAAAAGGAAAGGA | 286053 |
rs200788715 | in-del | -/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361068 | TGCCTTATGATTTCC[-/TT]TTTTTTTTTTTCGTT | 286053 |
rs200829910 | snp | C/T | 0.00170401 | 0.0291394 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151327 | TTACAACTCACTGAC[C/T]GAGAAGTAGAAACAC | 286053 |
rs200837390 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125151224 | GTTGAATTTGCTACA[C/T]TGGATCGGCAACTAA | 286053 |
rs200841138 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175731 | ATGATAATTGGAAGA[A/G]GAGGAGACTTTGACT | 286053 |
rs200847248 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314264 | CTTTCAAGGAGCCTT[G/T]TGTTTTGTTTTTGTT | 286053 |
rs200852105 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355305 | TGTCTGTATTATTTT[G/T]CCAAAATTAAAGAAG | 286053 |
rs200852872 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198365 | GAGATATGTTGCATC[A/G]ATACCTAGTTTATTG | 286053 |
rs200860351 | snp | C/T | 8.24545e-05 | 0.00642032 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125357780 | GGACGCCATTGTTCG[C/T]ATGATTGAGTCCAGG | 286053 |
rs200881955 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286318 | ACCTTTTATTTATTT[-/A]TTTTTTTTTTTTGAG | 286053 |
rs200882323 | in-del | -/TTTTTC | 0.175254 | 0.238565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240118 | AGCTGAAGTGTGCAG[-/TTTTTC]TTTTTCTTTTTCTTT | 286053 |
rs200886692 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218473 | CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 286053 |
rs200900777 | in-del | -/G | 0.162581 | 0.234218 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197048 | CTTTTTAATGGGGTT[-/G]TTTTTTTCTTGTAAA | 286053 |
rs200905590 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110958 | TCTTGTAATGGCAGG[A/G]AAAGAAACCCCTGTT | 286053 |
rs200930288 | snp | C/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161330 | TAATAATACAGCACT[C/G/T]TTTAGTGAAAATCAT | 286053 |
rs200932613 | in-del | -/AT | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212231 | TAGCAAGGCGAACAC[-/AT]ATTCATTTAAAGGTA | 286053 |
rs200943536 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324944 | CAGTTGTGTTGGAGT[G/T]GGGAGTAGAAGCCTG | 286053 |
rs200951990 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143197 | AGAAGGGTTTTTTTT[-/T]GTTTTGTGTGTTGCA | 286053 |
rs200953203 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202303 | CTTCTGCGTCGATCA[C/T]GCTGGGAGCTGCAGA | 286053 |
rs200958719 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140836 | AGAGAGAAGTGGCAG[G/T]TGTTGAAAATATGTT | 286053 |
rs200973319 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329946 | GTTGTTATTTTTTTT[A/C]TTACTATCACTTCTC | 286053 |
rs200976681 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315820 | TTCCCTCTCTTTTTT[A/T]AAGTCAGGGTTTCAC | 286053 |
rs201000042 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193557 | TAAAATGTATTTATT[C/T]TTCACTAGTTTTCTA | 286053 |
rs201010628 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337723 | AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 286053 |
rs201023097 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244229 | AGTAAAAAATGGCTG[G/T]TTTATAATTAGCATT | 286053 |
rs201025237 | in-del | -/C | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118353 | ACCACCGCACTCCAG[-/C]CTGGGTGACAGAGTG | 286053 |
rs201027278 | in-del | -/AAGG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304937 | AGAAAGAAGGAAAGA[-/AAGG]AAGGAAGGAAGGAAG | 286053 |
rs201028205 | in-del | -/A | 0.0659589 | 0.169201 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247173 | TCTCCAAAAAATAAC[-/A]AAAAAAAAAATTAGC | 286053 |
rs201030202 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304940 | AAGAAGGAAAGAAAG[A/G]AAGGAAGGAAGGAAG | 286053 |
rs201041012 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249995 | TGTTTACTTATTCAT[G/T]TATTTATTTTTGAGA | 286053 |
rs201044401 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111602 | GTCAGGAGTTCCAGA[C/T]CAGCCTGGCCAACAT | 286053 |
rs201045583 | snp | G/T | 0.000148254 | 0.00860844 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102454 | GGTATGGACACAGCT[G/T]CTAGTGTTGCTTTGG | 286053 |
rs201072149 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284210 | AGTAAAAAAAAAAAA[A/G]AAAAAAAATTTTAAG | 286053 |
rs201106220 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275031 | TAATAATAATAATAA[A/T]AATAAATAGAATAAT | 286053 |
rs201109459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199825 | TAAGTCTCTTTGTAG[A/G]TCTCTAAGGACTTGC | 286053 |
rs201113980 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340017 | TTTTTTTTTGTTTTT[-/G]TTTTTTTTTTTTTTT | 286053 |
rs201114737 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136194 | TTATGGCAGGTTTTT[G/T]ATAAACAGGAGAGTA | 286053 |
rs201115419 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315807 | GGTACCCTTTTTTTT[C/T]CCTCTCTTTTTTAAA | 286053 |
rs201130879 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218416 | GAAAAATTGAGGGTT[-/G]TTTTTTTTTTTTTGA | 286053 |
rs201132241 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272718 | TATATATATATATAA[A/T]ATATATATATACACA | 286053 |
rs201137883 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306360 | AAGCTTATATATATT[-/A]AAAAAAAAAAACTGA | 286053 |
rs201138822 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309723 | GTGAGACCCAGTCTC[-/A]AAAAAAAAAAATGTA | 286053 |
rs201143172 | in-del | -/T | 0.189261 | 0.242509 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091129 | CAGGGCCCTGGGAAC[-/T]TTTTTTTTTTCCCCC | 286053 |
rs201151703 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230704 | TTAATGGATAAAAGG[G/T]ACAAAGAAATTACCA | 286053 |
rs201152108 | snp | A/G | 0.000280748 | 0.0118446 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151317 | ATATATTTGGTTACA[A/G]CTCACTGACCGAGAA | 286053 |
rs201160022 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218626 | CATGTTGGCCAGGCT[A/G]GTCTTGAACTCCTGA | 286053 |
rs201166262 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197498 | GGTTTATCAAAGATC[A/G]GATGGTTGTAGATGT | 286053 |
rs201173239 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197983 | TCACTCATGATTTGG[C/G]TCTCTGTCTGTTATT | 286053 |
rs201176642 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351351 | GTGTACATTTTGTGA[A/C]ATAAAAAAAAAAAAA | 286053 |
rs201185071 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337939 | GGTTTGCCTGGAGAT[-/G]GCAGCATAAGGAGTC | 286053 |
rs201239486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301473 | CTACATGGAGGTGGC[A/G]GTGGGGTGGTGGTGA | 286053 |
rs201240768 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353963 | TTGAGACGGAGTCTT[-/G]CTCTGTCACTCAGGC | 286053 |
rs201267448 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242924 | TTAAGCTGCAGTCAC[-/T]TTTTTTTTTCTTTTG | 286053 |
rs201291957 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365789 | TTGAACCCAGGAGGC[A/G]GAAGTTGCAGTGAGC | 286053 |
rs201301432 | in-del | -/G | 0.0221141 | 0.102801 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216517 | GTGGCACATGCCTGT[-/G]AATCCCAGCTACGTA | 286053 |
rs201306938 | in-del | -/A | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207511 | ATTTTCAGTGGCTGT[-/A]GTTCAAAACTGCTGT | 286053 |
rs201338493 | in-del | -/AACT | 0.0185938 | 0.0946107 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272922 | ATACGGTGGAAAGAG[-/AACT]AACTGACTTGGGAGC | 286053 |
rs201345723 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330181 | TTTTCTTTTTTCTTT[-/C]TTTTTTTTTTTTTTT | 286053 |
rs201351269 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200368 | TTGTAAGGCAGGCCT[A/G]GTGGTGACAAAATCT | 286053 |
rs201359228 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355468 | ACTCTGGGAGGCCAA[A/G]GCGGGCAGATCACCT | 286053 |
rs201376919 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143489 | CATTTAATATTTATC[A/G]GAGTCTTCTGAGTAT | 286053 |
rs201410863 | snp | A/C | 0.00199806 | 0.0315443 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102518 | ACCTCTTTTGTGTCT[A/C]CTTTGAGGTAACACT | 286053 |
rs201421658 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326212 | CAGTGAGCCGAGATT[G/T]CGCCACTGCACTCCA | 286053 |
rs201429577 | in-del | -/CTTTT | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094843 | CCCTGGCGTCTCTTC[-/CTTTT]CTTTTCTTTTCTCTT | 286053 |
rs201447509 | in-del | -/TC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236380 | CTATATATATATATA[-/TC]ATATGATCCCATACA | 286053 |
rs201452146 | snp | C/G | 0.00199792 | 0.0315431 | missense | NSMCE2 | GRCh38.p7 | 8:125151236 | ACATTGGATCGGCAA[C/G]TAAACCATTATGTAA | 286053 |
rs201458991 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215198 | CCTCCCCCCTCCCCC[C/T]ACCCCACAACAGTCC | 286053 |
rs201466046 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262128 | AAATAAAATAAAATA[A/T]AAAATAAATTGTATA | 286053 |
rs201468095 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353797 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 286053 |
rs201470547 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217567 | GAGACAGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 286053 |
rs201480657 | in-del | -/ATAATAATA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275000 | GACAATCTGAAGATG[-/ATAATAATA]ATAATAATAATAATA | 286053 |
rs201495551 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201200 | TCATTCTCCGTCCAG[C/G]TTTGTTCCATTGCTG | 286053 |
rs201509313 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197019 | GGGAAGTGTCTGTTC[A/G]TATCCTTTGCCCACT | 286053 |
rs201533754 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322017 | TTCGTTCACATCAAT[-/A]TTTTTTTGTTTATTT | 286053 |
rs201539148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313131 | GGAAAGAAGGAAGGA[A/G]GGAAGGAGAAAGAAA | 286053 |
rs201548786 | in-del | -/AT | 0.0126979 | 0.078662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238706 | TTAAGATTTAAAATA[-/AT]ATATTTTTAAATAGT | 286053 |
rs201563478 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198707 | GCTAGCCTCATAAAA[G/T]GAGTTAGGGAGGTTC | 286053 |
rs201563612 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142261 | GAAGTAGTTACTGTT[-/A]ATTGTACCCATTATA | 286053 |
rs201570547 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197349 | TAACATTTAAGTCTT[C/T]AATCCATCTTGAATT | 286053 |
rs201578692 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218669 | CACCCGCCTCAGCCT[C/T]CCAAAGTGCTAGGAT | 286053 |
rs201600696 | in-del | -/TAAA | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093561 | AAATAAATAAATAAG[-/TAAA]TAAATAACATAATTG | 286053 |
rs201662658 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315122 | GAATCTTTTTTTTTT[C/T]TTTTTTCTTTTCATG | 286053 |
rs201670137 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224749 | TGCAATAAGGTAGGT[A/C]GATAGTGTTATCCCC | 286053 |
rs201696302 | in-del | -/GC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343493 | TTAAAGTATGAATTA[-/GC]CAGGCGTGTTGGCAC | 286053 |
rs201705712 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200875 | CTTTGTTTCTTTTTA[C/T]TCTTTTTTCTCTAAC | 286053 |
rs201714052 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201427 | CTTCTAACAATCAGG[A/T]CCCTCAGCTGCAGGT | 286053 |
rs201716197 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299832 | TTTTTTTTTTTTTTT[G/T]TCTTGAGACAGAGTC | 286053 |
rs201723981 | snp | C/T | 0.000884018 | 0.0210054 | utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125366924 | CACCAGCAGCCTACC[C/T]CCTACCCCAGCTGTC | 286053 |
rs201726287 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246220 | AGTCTCACTCACTCT[A/G]TCACCCAGGCTGGAG | 286053 |
rs201729858 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275032 | AATAATAATAATAAT[A/T]ATAAATAGAATAATA | 286053 |
rs201741648 | snp | C/T | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196203 | ATAACTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 286053 |
rs201748093 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233647 | TATTCCAAGACATCT[-/C]TTGTATTAATACAAG | 286053 |
rs201755991 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325304 | TTCTATTAAAATAAA[A/T]TAAAATAAAATAAAA | 286053 |
rs201780763 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161808 | AAAAAAAAAAAAAAA[A/C/T]CGGAAACGGTAACCA | 286053 |
rs201782232 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146853 | TATACATATGTAACA[A/G]ACCTGCATGTTGTGC | 286053 |
rs201789660 | snp | A/T | 0.0973687 | 0.197999 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250334 | AATGTTTTTCTTTTT[A/T]AAAAAAAAGCATCCT | 286053 |
rs201824679 | snp | C/G/T | 3.34325e-05 | 0.00408842 | missense | NSMCE2 | GRCh38.p7 | 8:125182118 | GTGAAAGAAGAACGT[C/G/T]CAGAAAAAATACCAG | 286053 |
rs201826673 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315817 | TTTTTCCCTCTCTTT[C/T]TTAAAGTCAGGGTTT | 286053 |
rs201826786 | snp | A/G | 1.69106e-05 | 0.00290775 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357192 | CGTTAGACCAGAGAG[A/G]CTTATCAACTCTCCA | 286053 |
rs201831023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333127 | ACCTGCCGAATCAGA[A/G]TCTCCAACAGTAGAC | 286053 |
rs201831230 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351191 | CTGAGTCATAACTGA[A/C]AAGCCACAAAAATTG | 286053 |
rs201886627 | in-del | -/TTTCCTTCTTTCCTTTCTTTATTTCCTTC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316618 | TCTTTCCTTTCTTTA[lengthTooLong]TTTCCTTCTTTCCTT | 286053 |
rs201903722 | snp | C/T | 0.000461338 | 0.0151808 | missense | NSMCE2 | GRCh38.p7 | 8:125151230 | TTTGCTACATTGGAT[C/T]GGCAACTAAACCATT | 286053 |
rs201908064 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357008 | AGATTCTTTTTAACT[G/T]CTCTGAGCCTCAGTT | 286053 |
rs201912405 | in-del | -/TG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340016 | GTTTTTTTTTGTTTT[-/TG]TTTTTTTTTTTTTTT | 286053 |
rs201921623 | in-del | -/CTCTT | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213610 | CTTTCCTTTCCTTTC[-/CTCTT]CTCTTATTTTCTCTT | 286053 |
rs201930510 | snp | C/T | 0.000741577 | 0.0192416 | missense | NSMCE2 | GRCh38.p7 | 8:125366794 | TTGGCTGTAGCCACA[C/T]GGATATAAGAAAGTC | 286053 |
rs201947087 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197943 | TAGGTATTTTATTCT[C/T]TTTGTAGCAATTGTG | 286053 |
rs201962611 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327948 | TTGAGGTTAGTATAT[A/G]TTAAAGAGCTCCTCC | 286053 |
rs201987635 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198445 | CATCTATTGAGATAA[G/T]CATGTGGTTTTTGTC | 286053 |
rs201994115 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179990 | TCCTATAATGTTACC[A/G]TTAACATCTTAGGTG | 286053 |
rs201999534 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248904 | GCCAGGCACGGTGGC[C/T]CATGCCTGTAATCCC | 286053 |
rs202000079 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271162 | GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATTGC | 286053 |
rs202005003 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314472 | ATTTTTTGTATTTTT[A/T]GTAGAGACGGGGTTT | 286053 |
rs202008942 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243495 | TTGCAAAAATAATAA[-/T]TTTTTTAAAAAAAAA | 286053 |
rs202024586 | in-del | -/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298697 | TGTGGGttttttttt[-/G]ttttttttttttttt | 286053 |
rs202029336 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217340 | TTTTAAAAAATTTTA[C/T]TTATTTATTTATTTA | 286053 |
rs202041767 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145275 | ATTGGGTACAGACAT[A/G]CAGGTTTATAGGATG | 286053 |
rs202046362 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212838 | CCGGGTTCTAATCAC[C/T]GAGGCATGTACCTGG | 286053 |
rs202059678 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340002 | CCTCCGACGTTGTAG[-/T]TTTTTTTTTGTTTTT | 286053 |
rs202061522 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200473 | TCTGGGTTGAAAATT[A/C]TTTTCTTTAAGAATG | 286053 |
rs202062678 | snp | A/T | 0.350109 | 0.229081 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286320 | CCTTTTATTTATTTT[A/T]TTTTTTTTTTGAGAT | 286053 |
rs202064815 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149819 | TTAGTGGCTTGTTTT[C/T]TTGTGTATTATAGGT | 286053 |
rs202069533 | in-del | -/TAAG | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093557 | AAATAAATAAATAAA[-/TAAG]TAAATAAATAACATA | 286053 |
rs202069595 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349584 | TGAGAGCTTGTATTT[A/T]AAAAAAAAAAAAAAA | 286053 |
rs202097376 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217617 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 286053 |
rs202104624 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150405 | TTGGTTTTCTTTTTT[-/C]TTTTTTTCTTTTCTT | 286053 |
rs202114090 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198011 | ATTGGTGTATAGGAA[C/T]GCTTGTGATTTTTGC | 286053 |
rs202116869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099688 | TTTTCAGGTGACCTT[C/G]ACAAGAGCAGTTGCA | 286053 |
rs202132273 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191410 | CCATTCATTTCTTGG[-/A]AAAAAAAAATTGACT | 286053 |
rs202151532 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286938 | TTTATCTCTGAACTT[C/G]AGTAGACGCCAATTG | 286053 |
rs202190152 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198560 | ATCGTGGTGGATAAG[C/T]TTTTTGATGTGCTGC | 286053 |
rs202205570 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197027 | TCTGTTCGTATCCTT[C/T]GCCCACTTTTTAATG | 286053 |
rs202207528 | in-del | -/TG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276765 | TAGTGTTATTCCTGT[-/TG]TACAGACAAGCAAAT | 286053 |
rs202236536 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156117 | AGACTCCATCTCTTT[-/A]AAAAAAAAAATGTTT | 286053 |
rs207469861 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330935 | AACTTTGTTCCCTTT[A/T]CTCATTAGATTTTTG | 286053 |
rs367547618 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252316 | GGCAGATCACAAGGT[A/C]AGGAGATTGAGACCA | 286053 |
rs367560281 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146558 | ACACCATGGAATACT[A/G]TGCAGCCATAAAAAA | 286053 |
rs367566549 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124156 | ATGTAATATGTGGTC[C/T]TTTGTGACTGGCTGT | 286053 |
rs367567405 | snp | A/G | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195705 | ACTGACCATCAACCC[A/G]CTTTACAGTATTTTG | 286053 |
rs367568053 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340012 | TTGTAGTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 286053 |
rs367580058 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134025 | ACAAGTTCCCAGTTG[A/G]TGGTGATGGTGCTGT | 286053 |
rs367580714 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146509 | CCCAAATGTCCAACA[A/G]TGATAGACTGGATTA | 286053 |
rs367588536 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117882 | TTTCAAGATTGTGTT[C/G]TCTTAATACAAATAT | 286053 |
rs367599553 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132718 | CAGGCTAGTCTTGAA[C/T]TGCTGACCTCAAGTG | 286053 |
rs367609348 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100253 | GAGTCGTAAAAGAGC[A/G]TAATAGAATCAGGAA | 286053 |
rs367611442 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155551 | CTATGCTTAGTAATG[-/G]CAAGTCATGGCAGTA | 286053 |
rs367652126 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111272 | GCCCTCATGAATAAC[-/T]GACCTTTTACATTTG | 286053 |
rs367670110 | in-del | -/CAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178012 | GTCTTCCTCTCACAA[-/CAA]GAGTTGGTGATTCTG | 286053 |
rs367685094 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294577 | TATTTTACCAATCTA[A/G]GGCTAAACTTGCGAT | 286053 |
rs367701720 | in-del | -/GAAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313244 | GAAGAAAGAAAGAAA[-/GAAA]AGAAAAGAAGGAAAG | 286053 |
rs367728277 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270856 | AGATCACACTTGTGA[A/C]CAGCCACTGCACGCC | 286053 |
rs367770400 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257145 | AAAAATTAGTCAGGC[A/G]TGGTGGCACGTGCCT | 286053 |
rs367789617 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352751 | TTACCAGACTTATCA[C/T]AAAGTTTTGTCTTTG | 286053 |
rs367812540 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354576 | AGCTGGAAGCCCCGA[A/G]GCACTGCACCTTAAT | 286053 |
rs367825184 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334149 | TGTTCAGTTCACTTT[C/G]TCCTTTACTCAGAGT | 286053 |
rs367832078 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299188 | TATATAGTGAAATGC[A/G]TGAGGTTATCAATAG | 286053 |
rs367837062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221497 | AGTCCACCTGCCTCA[A/G]CTTCCCAAAGTTCTG | 286053 |
rs367875403 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312090 | TAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA | 286053 |
rs367880647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271951 | ACCCAGAGATATTCG[G/T]TGACTTGGCCAAGGC | 286053 |
rs367931800 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146135 | GTGTTGTTTTATGCT[A/G]ACAGATTGCCAACGG | 286053 |
rs367942891 | in-del | -/GATCAGTG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216203 | GTACCACATTTTGTT[-/GATCAGTG]GATCCACTTATCTGT | 286053 |
rs367957117 | in-del | -/CTTCGTCTTTTATC | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100375 | CTTCCATCTGTTAAA[-/CTTCGTCTTTTATC]CTTTAAACTCAGTTC | 286053 |
rs367961402 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333640 | CTGCCTCAGCCTCCC[A/G]AGTAGCTAGGACTAC | 286053 |
rs367972009 | in-del | -/AAAGA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313241 | AAAGAAGAAAGAAAG[-/AAAGA]AAAGAAAAGAAGGAA | 286053 |
rs368008511 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207164 | ACCAGTTTTTTTTTT[-/T]CTCTGCTTCTACTTC | 286053 |
rs368023213 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100998 | TGGTATTCTCATGCT[A/G]AAGGAAGTGCCTGGC | 286053 |
rs368064623 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347910 | GTGGCAATGAATGAA[A/G]TGCTTACATTTAAGG | 286053 |
rs368067132 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214460 | GGGGGCTCACGGTCT[C/T]AACAAGGAAATGGGT | 286053 |
rs368068473 | snp | A/C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282464 | AAATTTGAAATGCAA[A/C/T]GTTTAGCTAAACAAA | 286053 |
rs368068745 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227007 | GCCCCCTTTGCCTAG[C/G]GACTCACCAGTGAGT | 286053 |
rs368072705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205779 | GAGAAAAAATGGTTA[A/G]AATTATAGGTTGTAA | 286053 |
rs368080885 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308328 | TTTTGGGGGGAAAAA[-/A]TCCTAAGTAAAACCT | 286053 |
rs368114935 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251393 | TGGAAAATTATATCA[C/G]GGGTCTTAATGGGAA | 286053 |
rs368182115 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257139 | AAATACAAAAATTAG[C/T]CAGGCGTGGTGGCAC | 286053 |
rs368188897 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215675 | GGTTTTAGGTCTAAC[A/G]TTTAAGTCTTTAATC | 286053 |
rs368201749 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263848 | ATATCAGCTCTAGCG[C/T]GTAAAGAGAGATTTT | 286053 |
rs368237634 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212561 | GGAGGGTTCAGGTAC[A/G/T]TGTTCAGTACCAAAC | 286053 |
rs368237720 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238349 | AGTTATAGAAAAAAA[-/A]TAAAGCACAAGTTCT | 286053 |
rs368269789 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108568 | AAATGCCTGCTTCAT[A/T]AGATTGTTGGGACTA | 286053 |
rs368303019 | snp | A/G/T | 0.000103371 | 0.00718858 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357178 | TTCCTTTTCTTTGAC[A/G/T]TTAGACCAGAGAGGC | 286053 |
rs368305015 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175550 | CATCTAACAATGGCT[-/G]GTTTTGGAGAAAGTC | 286053 |
rs368329204 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315966 | CACCACCACATCCAG[C/T]TAATGTATTTTTTGT | 286053 |
rs368356626 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244717 | AAAAATTCAGTAAAC[A/C]CTGTCAAAGCAATCC | 286053 |
rs368437346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281532 | GCAGCCTCCACCTCC[C/T]GGGTTCAACCGATTC | 286053 |
rs368438849 | snp | A/G | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367284 | CTTTGGGAAGCCGAC[A/G]TGGGCAGATCACTTG | 286053 |
rs368451802 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358514 | TATACACACACACAC[A/T]TATATATATCTCACC | 286053 |
rs368454433 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295746 | TGGAGCTTGAATTTT[C/G]TCTCCTCCAAAGTAA | 286053 |
rs368454998 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205030 | TCTCACCGCTCTCCT[C/G]TCTAGCCCTTGGAAT | 286053 |
rs368456797 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252739 | TGCTTATCCATTTCT[A/G]AATTATTTTAGAATG | 286053 |
rs368471148 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134260 | TCTGAGTCATTATGA[C/T]GAGATTTCATTATAT | 286053 |
rs368488591 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146663 | AGAAAACCAAACACC[A/G]CATGTTCTCACTCAT | 286053 |
rs368504662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240369 | ACCTCGTGATCAGCC[C/T]GCCTTGGCCTCCCAA | 286053 |
rs368529215 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257290 | CTCCATCTCAAAAAA[A/G]AAAAAAAAAAAAAGA | 286053 |
rs368539172 | snp | C/T | 1.65781e-05 | 0.00287902 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357339 | CGCTTCCTCCTACTT[C/T]CCCTGAAAGAAACAC | 286053 |
rs368547100 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322682 | AGTAAAATTTGCAGA[C/T]AACATGATCATCTGT | 286053 |
rs368578036 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126577 | AGTACCTTACTTGAT[G/T]CACGAAAGTCCTATT | 286053 |
rs368579308 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260684 | GGCTGGAGTGCAGTG[A/G]TGTGGTCTCAGCTCA | 286053 |
rs368595826 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116165 | GACATCCAGTTCTTA[C/T]TGCAAATATATGAGG | 286053 |
rs368601773 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225978 | AAAGTGAATCCTTGA[G/T]TCTCTGAAGTTGCCC | 286053 |
rs368603534 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139973 | ATTTCTGCTGTTTCT[A/G]TAAGTATTTGAATTT | 286053 |
rs368631455 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307565 | TTGTGAAGCCACTGA[A/G]CATCACTCTCACTGA | 286053 |
rs368633157 | in-del | -/C | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284700 | TGAATCTGAATCTAA[-/C]AGAGAGGGCTTTATT | 286053 |
rs368643668 | in-del | -/ACTG | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129636 | CTGGAATGATGTCTG[-/ACTG]GTGCCTTATTTACAT | 286053 |
rs368647033 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294409 | ACTGCGCCATTTTAC[A/C]TTCCCACCAGCATTG | 286053 |
rs368657809 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174688 | TTTCACAATTTTTCC[A/G]AAAGGCTCGAAGGAG | 286053 |
rs368687583 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135327 | AGTAGCTGGAATTAC[A/G]AGCTCGAGCCTCTGT | 286053 |
rs368721263 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276595 | ATATCTGATTGTATA[C/T]ACAGTCCCTCATAGA | 286053 |
rs368736347 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105473 | ACAGAGTTTTTTTTT[-/T]CTCTTGGTTTTGTTT | 286053 |
rs368745029 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323998 | AAGATTTTGAAAAGA[-/T]ACTGAAATGAACAAC | 286053 |
rs368770781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149409 | GGTATTATTCTTCAG[A/G]GTAGAAAAGAAAAAC | 286053 |
rs368789622 | in-del | -/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192343 | GGTTTTTTTTTTTTT[-/TT]AAAGAAAGTTTAAGT | 286053 |
rs368813666 | snp | C/T | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093093 | TGTGGGCTTCTGTAA[C/T]GGAAATGCCATAAAC | 286053 |
rs368864859 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121512 | AAGGCAAATAGGTAT[C/T]CATGCAAAGATCAGG | 286053 |
rs368877914 | in-del | -/TTCCTTAT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213737 | TATTTCCTTCCTTCC[-/TTCCTTAT]TTCCTTCCTTCAACT | 286053 |
rs368883776 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102381 | TGGTTTCATCTCCTT[C/T]AGTGGTGTAGAGTCT | 286053 |
rs368887667 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299124 | TGAAAGTAAACCTTT[G/T]AAGTATTTTTATAGC | 286053 |
rs368892286 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134890 | ATGCCACCATACCCA[A/G]CTAATGAAAAATAAA | 286053 |
rs368897247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255729 | GTGTACACACAGCTT[A/G]TTATTTTCATTATTG | 286053 |
rs368910356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296686 | CAGATGTGAGTCACC[A/G]CACCCGGCCTGCTGT | 286053 |
rs368917655 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253966 | CTATAAGATTATCCT[A/G]GTGTTCAGGATGCTT | 286053 |
rs368934117 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197745 | AGTCATTGGTAGCTT[A/G]ATGGGGATGGCATTG | 286053 |
rs368981068 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289041 | AAGCAATCCTGCCTT[A/G]ACCTCCCAAAGTGCT | 286053 |
rs368990113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188024 | ATTTTGAATGACAAT[A/G]ATATTTGTATCAGAC | 286053 |
rs368996805 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260403 | GATTACAGTGTAGGG[C/T]GGTTCATTTTGATTC | 286053 |
rs368996867 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176737 | CACTATACATTGTCT[C/T]AAAAACCAGAAAAAT | 286053 |
rs369004159 | in-del | -/AG | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170911 | TTTAAAAAGAAAATC[-/AG]AGGTTTTTACTACTC | 286053 |
rs369017609 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277847 | TTAAATTTAGCAGTC[A/G]TTACTGAGAAATCAT | 286053 |
rs369022330 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302009 | CTCTTGCCCAAGCTG[A/G]AGTGCAGTGGCACAA | 286053 |
rs369024542 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256277 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAAA | 286053 |
rs369032349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193206 | TAACTACACATTTAT[A/G]TAAAGTAGACTTCAT | 286053 |
rs369041673 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231842 | CTACCATGCACCTCT[A/T]GAAAGAAGGAACACA | 286053 |
rs369050721 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114904 | AATACTTGGACCTTT[A/G]TTGCTCTTTTTGCTG | 286053 |
rs369077276 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157741 | GATTTTCACCGTTAC[C/G]TCATAGAAATCCATC | 286053 |
rs369088009 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248402 | CTGAAACTGCAAGGG[G/T]CAAAATTAATATCAT | 286053 |
rs369090741 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309503 | CAATGGGGGAGGATC[A/G]CTTGAGCTCGGGAGT | 286053 |
rs369094769 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190095 | ACTTTTTCAGGCTGG[A/G]TTGCATCCTGAGAGC | 286053 |
rs369123179 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273472 | GTTGCACAATACTTT[A/C]ACAATGCCTTCCTGG | 286053 |
rs369124390 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147993 | TCTCTCAGCCCCCTG[C/G]TACAGCTGACCAAGA | 286053 |
rs369147813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124576 | CCTCAACCTTCTAGG[C/T]TCAAGCAATCCTCCC | 286053 |
rs369149163 | in-del | -/CA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209411 | CTTTCCTAAATTTGA[-/CA]GGTAAATTTGCTTTT | 286053 |
rs369150458 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239406 | TTGAGGCCAGGATTT[C/T]GAGACTAGCCTGGCC | 286053 |
rs369208929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331789 | CGGTAAAGTTTCAGC[A/G]TATAGCATGGTCCAC | 286053 |
rs369210820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285322 | ACAAGAAGTTTTCAT[C/T]ACATTCAGTGGCTTG | 286053 |
rs369276745 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253561 | GGGATTTTGTAGTTT[C/T]TCAGATGTTATACTG | 286053 |
rs369287804 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197692 | CTTTTTTGGTTCCAT[A/G]TGAACTTTAAAGTAG | 286053 |
rs369305452 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120641 | TGTACTCTAGTTGCT[A/G]TAAACAATTAGGCCT | 286053 |
rs369310503 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360402 | CAGAGAGCCAGCAAG[G/T]CAGGACCCGCACCTC | 286053 |
rs369321830 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151008 | GAGGAGGTTTTTTTT[A/T]TTTTTTTTATTTTTT | 286053 |
rs369355689 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117579 | GGGTCTTACTCTGTC[G/T]CCCAAGCTCACAGTA | 286053 |
rs369414766 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098280 | GAGGACTTGTTAAAA[C/T]GTAGATTGTTGGGGC | 286053 |
rs369446234 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171402 | TAACAGACCTGCTAA[G/T]GCAGTCAGTCCTAGC | 286053 |
rs369451300 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341120 | AATTTTTAGCTAAGG[A/G]ATAAAAGTGTAGTTA | 286053 |
rs369452051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108456 | AAGTGCACGCTTGCT[A/G]TTGGGTCCAGTCCTA | 286053 |
rs369456142 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266992 | AAAAGCATAACTTTT[C/T]TTTTTTCTTTCTTTT | 286053 |
rs369462971 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114193 | TTTATTTTTCTCTCG[A/G]CTGTTTAATACTTAC | 286053 |
rs369480402 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211285 | CCCTGGAAACAGTTA[A/C]TCTTACCAGTTCCTT | 286053 |
rs369503628 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164097 | ATTTGTAAGTATCAT[C/T]AGTTCATACTCCAGT | 286053 |
rs369523582 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354574 | AAAGCTGGAAGCCCC[A/G]AGGCACTGCACCTTA | 286053 |
rs369548797 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279098 | AAAAGTTTAGAGTTG[C/T]CAGTTAAATACATAT | 286053 |
rs369550633 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337026 | GACATAGGCTTCTTA[A/T]TGTTTGTGAAATTAT | 286053 |
rs369561568 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202966 | ACAACCTTTTCTTGA[G/T]AGGAAGACAGAAACT | 286053 |
rs369586888 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266455 | AAAATAGTTCATAAC[A/G]AGAACAAACACAATT | 286053 |
rs369596198 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216336 | TATCAGAAGTGGAAT[A/G]GCTGAATCAAATGAT | 286053 |
rs369604813 | in-del | -/TAAAATAAAATAAAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325310 | TAAAATAAAATAAAA[-/TAAAATAAAATAAAG]TAAAATAAAATAAAA | 286053 |
rs369622865 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356348 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCGCT | 286053 |
rs369631578 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143469 | TGGACATATGTACTT[A/T]ATGACATTTAATATT | 286053 |
rs369675300 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315526 | CCCTCATGGGCATGT[A/G]AGGATTCAACTAGCT | 286053 |
rs369702808 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106551 | GGCGTGGTGGTGCGC[A/T]CCTGTAATCCGAGCT | 286053 |
rs369711853 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364058 | AAGTGATTTTCCTGC[C/T]TCAGCCTCACGAGTA | 286053 |
rs369791999 | in-del | -/AACATGAGCTGAGT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225139 | TATGTGCTAATCCCT[-/AACATGAGCTGAGT]TTGAGAACTTAATGT | 286053 |
rs369792049 | in-del | -/GT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183635 | ATTTATTACTCAGTG[-/GT]GTGTGTGTGTGTGTG | 286053 |
rs369815347 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331286 | GCCTGGGTGACAGAG[C/T]GAGACTCCGTCTCAA | 286053 |
rs369827225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284887 | GTAGGCATTCTTTTT[A/G]TAGCTAATGTGCTAA | 286053 |
rs369833755 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313466 | AAGAAGGAAGGATCT[C/G]TATGCCAAATCTCAA | 286053 |
rs369840545 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131280 | TACTTGGAAAATATA[C/T]GCACTGAAGACATAC | 286053 |
rs369845619 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286311 | AAACAATACCTTTTA[-/T]TTTATTTTTTTTTTT | 286053 |
rs369891126 | in-del | -/T | 0.103438 | 0.202533 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185305 | CCATTACATTTTAAA[-/T]TTTTTTTTTTCTTTT | 286053 |
rs369922036 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278765 | GTCCCAGAAGCTGAA[A/T]TTCACTTCCACCTGT | 286053 |
rs369945546 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180558 | GAATTCATATGCATT[C/G]ATAACTCAGATTCAG | 286053 |
rs369953883 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171337 | CTCTAATAGGCTCTA[A/G]GTAAATAGTTGAAGT | 286053 |
rs369975416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338360 | GATGAACAGAATGCA[A/G]AAGTTTCTTCCTGCA | 286053 |
rs369982766 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323845 | TTCTTCAAGAGATAC[C/T]CTTAGGAGAATGAAA | 286053 |
rs369992841 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106888 | ATAATCCCGGCTACT[C/T]GGGAGGCTGAGGCAG | 286053 |
rs369997721 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154882 | ACCTGATGTTTCCTC[C/T]CTTGCTTTCTACGCT | 286053 |
rs370003867 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130977 | CTAGCTTAGGGTTTA[C/T]GGACAGTTCTTTTGC | 286053 |
rs370011425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097952 | TTCCTGCTTTTTTCT[A/G]TCTTTATTACTGGCA | 286053 |
rs370024951 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112067 | TTTCTAGTGGTGAGT[C/G]GTGGCCACAATGATA | 286053 |
rs370085866 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257150 | TTAGTCAGGCGTGGT[A/G]GCACGTGCCTGTAAT | 286053 |
rs370117622 | in-del | -/GAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285264 | TATACCAGAGCTTAG[-/GAG]AATAAAAATAAGTCA | 286053 |
rs370126170 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257120 | GAAGCCCCATCTCTA[C/T]TAAAAATACAAAAAT | 286053 |
rs370133431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201869 | TCAAGCTTCTCAGCC[A/G]CTTTGTTTACCTACT | 286053 |
rs370140284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139073 | GGCGCTGAATCAGCT[C/G]TGTCTTTGGAAGGAC | 286053 |
rs370157850 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290475 | TTGCATTTTTTTTTT[-/T]CTTTCTCTCAGCCTG | 286053 |
rs370160022 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327237 | CACCACTGCACCCCA[G/T]CCTGGGCGATAAAGC | 286053 |
rs370196764 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340083 | GCAGTGGCGCAATCT[C/G]GGCTCACTGCAAGCT | 286053 |
rs370207873 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176822 | TTACCTGGCAGCAGA[C/T]ATCGGCAGCTGAGTA | 286053 |
rs370219528 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304011 | TTGGCTTTGTCATAC[A/G]TGAGATTTTCATCTT | 286053 |
rs370222357 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276063 | TGTCCTGCTGTAGTG[C/T]TCAAGATGTCTGCCA | 286053 |
rs370227029 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325694 | CAGTGGCTCACACCT[A/G]TAATCCCAACACTTT | 286053 |
rs370230256 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298871 | AAAACTCAGGACAGT[C/G]TTAGTATTGATGGGA | 286053 |
rs370235435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255606 | AATTATGAGCACTTA[C/G]GTGTTGCTGGAGCTT | 286053 |
rs370290327 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157348 | TAGACAACTCTTAAC[A/G]TGTTTCTTATCAAAA | 286053 |
rs370290420 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251012 | TAATTTATGATATGC[C/T]GTGCAGAAAAATTAT | 286053 |
rs370316983 | snp | C/T | 1.64895e-05 | 0.00287132 | missense | NSMCE2 | GRCh38.p7 | 8:125357776 | AAGAGGACGCCATTG[C/T]TCGCATGATTGAGTC | 286053 |
rs370337268 | in-del | -/ACCAAAAAACTTTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234951 | CAAGTCCTGGCTTTT[-/ACCAAAAAACTTTT]CCCTGGCCAGGCGTG | 286053 |
rs370355536 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285906 | TCACATGTATGTCTC[A/G]GTGACTGTGCCAGGA | 286053 |
rs370360736 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199787 | GGGGTGTTAAAGTCT[C/T]CCGTTATTATTGTGT | 286053 |
rs370371468 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343202 | AGGGGACATACTCCA[G/T]TCATTACAATCTGAG | 286053 |
rs370379285 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303552 | ACTGGGTGCCAAGAA[C/T]GTCAAAATAAGTGGC | 286053 |
rs370385258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294307 | TTATTTCCATTTCTC[A/G]TGGTATTTATCTCAC | 286053 |
rs370387035 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340051 | ACGGAGTCTCGCTCT[A/G]TGGCCCAGGCGGGAG | 286053 |
rs370387773 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093510 | CCTGGTCAACATAGC[A/G]AAACCCTCTCTCTAC | 286053 |
rs370395432 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186578 | TATAATATGACAACC[A/G]TTAATAACAAATATC | 286053 |
rs370425585 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213054 | AAATGATGATTGGCT[A/G]CCATTTAATTCTCTT | 286053 |
rs370442915 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115489 | GGCTCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 286053 |
rs370496190 | snp | C/T | 1.74442e-05 | 0.00295327 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357857 | TGGAGCCTTCCCTAG[C/T]GGTAGTTACTCAGAG | 286053 |
rs370498996 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182797 | TAAACTATTACATTC[A/C]AGTTTTTTAGTGGAC | 286053 |
rs370499640 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346417 | GTGGTACTTACAACT[C/T]TCTAAAATAAGAGAA | 286053 |
rs370502051 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239895 | AGAGTAGAGTGAGTC[A/T]GAGAAAGATGGTCAC | 286053 |
rs370530811 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218948 | CTACTATATAAGGAC[A/T]CCATTTGGTCTCTGC | 286053 |
rs370536102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305125 | CCAGCTTCAGAGGTT[A/G]GATAAATGGAGATAT | 286053 |
rs370545927 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258048 | AGAGAAGAAAAAGAA[G/T]ATGTGATTCATGTAG | 286053 |
rs370549275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173523 | TGATCTTCTAGATGA[C/T]AGGGTATGTGGTAAG | 286053 |
rs370560109 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333553 | GGAGTCTCGCTCTGT[C/G]GCCCAGGCTGGAGTG | 286053 |
rs370571754 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316084 | AGTGGTGGGATTATA[A/G]GTATGAGCCACTACA | 286053 |
rs370584966 | snp | A/G | 1.65263e-05 | 0.00287452 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357325 | CATTACAAAGGTACC[A/G]CTTCCTCCTACTTCC | 286053 |
rs370620230 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269127 | AGTCCCACTCTGTCA[A/C]CCAGGCTGGAGTGCA | 286053 |
rs370636546 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288064 | CTTCTGGCCTCAAGC[A/G]ATCCTCCTGCCTCAG | 286053 |
rs370659339 | snp | C/T | 0.34303 | 0.232046 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316703 | TTCCTTCTTTCCTTC[C/T]TTCCTTCTTTCCTTC | 286053 |
rs370664915 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134453 | CAGTCTTCTTACTTT[C/T]AGCCATTCTAATAGA | 286053 |
rs370666970 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255060 | CAGCGTCCACTTCCT[A/G]TCTCCTTGTATGCTC | 286053 |
rs370677518 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319469 | GATTGCATTCCATAT[A/G]TTCAGAAAACTATAA | 286053 |
rs370681920 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298687 | AAATTCATCTGTGGG[-/T]TTTTTTTTTGTTTTT | 286053 |
rs370700789 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124995 | AGATGGGGTTTCACT[A/C]TGTTGGCCAGGCTGG | 286053 |
rs370705310 | snp | A/G | 0.0134861 | 0.0810011 | utr-variant-5-prime, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091668 | GGAGGTCGCGCGCGG[A/G]GCCGGCACCCAGTTT | 286053 |
rs370718690 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157076 | CCACTTACTGACTGA[A/T]TATAAGAATATACCC | 286053 |
rs370728280 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356366 | ACAGAGTCTCGCTCT[A/G]TCACCAGACTGGAGT | 286053 |
rs370733026 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225576 | AAAGTCTAAGGGTAC[A/G]GTGAGCAGAGAAGCC | 286053 |
rs370745523 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249579 | GCCACCTACTCACTT[C/G]ACCAACATACATTTT | 286053 |
rs370770152 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218382 | CTCCACATGCATTTG[C/G]GATAAAAATAGCATA | 286053 |
rs370800354 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347815 | GATAGCTTCACCACG[C/T]ACATAGAATCTGAGA | 286053 |
rs370822108 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131728 | TGTATATTTTAAAAA[G/T]GCAAAATTGGAGCTT | 286053 |
rs370830181 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320260 | GAGGGAGGGAAGGAA[-/G]GGAAGGAAGGAAGGA | 286053 |
rs370837946 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205362 | GCTTTGAAATATCCT[A/G]ATTATTTCATTTAAA | 286053 |
rs370849364 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121311 | AGATTTGCGCTTCCT[C/T]TTCTTTTGGGCAGGT | 286053 |
rs370856184 | in-del | -/CT | 0.188631 | 0.242351 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239602 | GGCGACAGAGCAAGA[-/CT]CTGTCTCAAAAAAAA | 286053 |
rs370877320 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347351 | ACACCTCCCTGGAGA[A/G]CCTGGCTGAGTCATT | 286053 |
rs370881450 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216208 | CACATTTTGTTGATC[A/C]ACTTATCTGTCAATG | 286053 |
rs370895566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107841 | GAGTTTGATACTAGC[C/T]TGCAGCAACATGGCA | 286053 |
rs370907705 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332852 | TAGTCTTATGAACCA[A/C]CCTTTGATTTCAAAA | 286053 |
rs370918621 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307640 | CTTCCAAGAGGAAGC[C/T]ACAGGGTTGTAGGCT | 286053 |
rs370933285 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151682 | ATTGCCAAATTCTTA[A/G]AATCAGATAATATGG | 286053 |
rs370936553 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305998 | GCTTGAGAGTCAATA[-/G]CCAGGCAATTAGGAT | 286053 |
rs371047331 | multinucleotide-polymorphism | CTC/TTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359334 | TTGCTCTTTCTCTTT[CTC/TTT]TTTTTTTTTTTTTTG | 286053 |
rs371052622 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249472 | CTCAAGTTTCATTCA[A/G]CTGACAAAATAACTT | 286053 |
rs371065331 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100706 | GCTGGGATTACAGGT[G/T]CCCACTACCATGCCC | 286053 |
rs371068057 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122855 | ATCCTGTTTCCCAGC[C/G]AAGTTGGGGCTTCGT | 286053 |
rs371119927 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095902 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAATTGAAT | 286053 |
rs371165290 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194339 | TGTTGTATAGGTAGA[A/C]TTGTACAGTGTGTAG | 286053 |
rs371231274 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183419 | TTTTGTTCTTTTTTT[-/T]AACATCACAGCTCCC | 286053 |
rs371244244 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280646 | TGAAGTCCAGCTGAT[A/T]ATAATAAAAGTGATA | 286053 |
rs371248841 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272919 | TGTAATACGGTGGAA[A/T]GAGAACTGACTTGGG | 286053 |
rs371260884 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354733 | GAAGGTGACTCTCTA[A/G]GAAAAACAAAGTAAT | 286053 |
rs371268317 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330328 | TTACAAGCGTGTGCC[A/C]CCACACCCGGCTAAT | 286053 |
rs371272885 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257147 | AAATTAGTCAGGCGT[A/G]GTGGCACGTGCCTGT | 286053 |
rs371276570 | in-del | -/AT | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098986 | TACAGTTTTGGAGAC[-/AT]GTGCTGTTTTAGGTG | 286053 |
rs371286579 | in-del | -/A | 0.330947 | 0.236533 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235244 | GACTCCATCTCAATT[-/A]AAAAAAAAAAAAAAG | 286053 |
rs371290493 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224489 | TTTGCATATATTGTG[A/G]GTTAACAGTCTAATT | 286053 |
rs371294885 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139765 | ACACAGCCAAACTAT[A/G]TCATCTTCCCACATA | 286053 |
rs371300984 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177402 | ACAAGTATCTTTAGC[A/C]CTCTCATTCCCATGA | 286053 |
rs371301932 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094366 | TACTTAGCTGTATTT[A/G]TTGGGAGAGATTGAG | 286053 |
rs371304196 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114163 | CCTTTCAGAATCTCT[C/T]ACCCCTTTCTCTGCT | 286053 |
rs371330940 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265553 | TTTTTAAATTATTGC[A/G]TTAAAATGCTGCTAT | 286053 |
rs371332983 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231971 | TGAAATGAAAGTCAC[C/G]TGACTCCTCTGAACC | 286053 |
rs371363333 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221879 | AAGCATTTCAGATTT[G/T]GGGATTAAGGATGTT | 286053 |
rs371392161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351551 | CCGGCATATGCTTCT[A/G]ACAACATCGTCTATG | 286053 |
rs371399215 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205932 | CTCTTTAATATATTG[G/T]CCTGGTAAGTGTGCT | 286053 |
rs371432421 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268280 | AAGGTCAACATTTGG[-/T]TAGTGAAATTAGAAA | 286053 |
rs371461527 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333755 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 286053 |
rs371475617 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331024 | GAAAGAAAGGTGACT[A/G]GGCGCGGTGGCTCAC | 286053 |
rs371494633 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282886 | GAAAATATTTTTACC[A/G]AAATTATGGATGGAA | 286053 |
rs371558182 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268549 | TGATGAGTAATTAAA[A/C]TATTCCTTAGGTTGT | 286053 |
rs371560105 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296559 | ACCACCATGCCAGGC[C/T]AATTTTTTTGTATTT | 286053 |
rs371582991 | in-del | -/GAGT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312999 | TGATCAAGAGACAGT[-/GAGT]AGAGGATGGGTCAGT | 286053 |
rs371592977 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259713 | TAGTAATCATAATAT[A/T]AACAATAGCTTATAT | 286053 |
rs371602277 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110973 | AAAAGAAACCCCTGT[A/T]TGGCTAAGCAACAGC | 286053 |
rs371607273 | in-del | -/TAGCGTGTAAATCAGCTCTAGCGTGT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263830 | TCAGGAATCCCTCTC[-/TAGCGTGTAAATCAGCTCTAGCGTGT]AAATATCAGCTCTAG | 286053 |
rs371624438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103375 | ATTTTATTTTACACA[C/T]GGAGCCAGAGGAGCA | 286053 |
rs371634190 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306032 | AGGTCATAGTATTGA[A/G]TAAGTTTATACTTGG | 286053 |
rs371650886 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257140 | AATACAAAAATTAGT[C/T]AGGCGTGGTGGCACG | 286053 |
rs371690065 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341249 | GATGTCATTCACATG[C/T]CAGGCTGTAGATTAT | 286053 |
rs371710022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124239 | ACTTTATTCCTTTTT[A/G]TAGCTGAATAATATT | 286053 |
rs371726001 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141543 | AATAACACTGAATTC[A/G]TGTTGTTGTAACAAA | 286053 |
rs371745204 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301394 | ATACTGGCTTTGTGA[A/C]CTTTGCAAATTCACC | 286053 |
rs371746493 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146278 | CACAGGTGGGCAAGT[G/T]TACAGACTTGGCAGT | 286053 |
rs371753899 | in-del | -/AGGGA | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126471 | GCACCTGGCAGGTTC[-/AGGGA]ACTGCATGTTAACTT | 286053 |
rs371754515 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256118 | GAAATCCCTGTCTCT[A/G]CTAAAAATACAAAAA | 286053 |
rs371759755 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231329 | TTGTCTTCATAGCTC[A/G]TCAGTGAGTTCACAG | 286053 |
rs371778623 | in-del | -/AGCCTGGAAC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150884 | TGTAAGTAAGGGCAC[-/AGCCTGGAAC]TCCTTAATACAAGTC | 286053 |
rs371803054 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326150 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAAGCAGG | 286053 |
rs371862968 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259005 | CCTCTTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 286053 |
rs371870142 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281687 | TCAAGCAATCTTACC[C/T]GCCTCAGCCTCCCAA | 286053 |
rs371879423 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237043 | TTTTAATATTCTTCT[G/T]TACCTGGCACAGCAG | 286053 |
rs371891299 | in-del | -/AT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175824 | AGAAATGAGTTATAT[-/AT]TATCATCATATAAAT | 286053 |
rs371899118 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357924 | GTCTCTTCTAAATTC[C/T]GTTCACCTCCCGAAT | 286053 |
rs371935341 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176261 | TCTTGCTAGAGTCTC[A/T]AGTGACTCAAAAATC | 286053 |
rs371936126 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221010 | AAGGGATACTATCAC[C/T]CTTCCTCAGAGCTAG | 286053 |
rs371945266 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251441 | GGGAGAGACTTGAAT[A/G]TGATTAAATATTAAT | 286053 |
rs371956150 | in-del | -/GT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319523 | ATACATGGAAGGTAG[-/GT]GTGTGTGTGTGGGCA | 286053 |
rs371967084 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134395 | GGAGTATATTAAGGG[A/T]ACTCTATAGTCGCTC | 286053 |
rs371980467 | in-del | -/GTTTTGTTTTTGTTTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314287 | TTTTTGTTTTGTTTT[-/GTTTTGTTTTTGTTTT]TTGAGACAGAATTTC | 286053 |
rs371983263 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238646 | GATAACTAAATCTCA[C/T]CATGAATTTGTTGGG | 286053 |
rs372016316 | snp | C/T | 3.33723e-05 | 0.00408473 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357201 | AGAGAGGCTTATCAA[C/T]TCTCCATTTTCCTCT | 286053 |
rs372017951 | in-del | -/AGGGAGGGAGGGA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320221 | GAGAAGGAAGGAAGG[-/AGGGAGGGAGGGA]AGGGAGGGAGGGAGG | 286053 |
rs372045770 | snp | A/G | 0.000381689 | 0.0138094 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102286 | ATTATTCTGACTTAC[A/G]AATCTTGTTTCATTG | 286053 |
rs372046745 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282914 | GAAACTATGAGAATC[A/G]TTCTGATGAGGGCAT | 286053 |
rs372096378 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155725 | ACTAAACCTATAGTT[C/G]CAAACTGTGGGCTTC | 286053 |
rs372104968 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102717 | CTGCGCTAGAAATGT[A/G]TGGGCAAAGATTTGA | 286053 |
rs372108609 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263730 | ACACCAGCCTCCGTG[A/G]CAGAGCGAGACTCCA | 286053 |
rs372121311 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257151 | TAGTCAGGCGTGGTG[A/G]CACGTGCCTGTAATC | 286053 |
rs372125721 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194917 | TGTTCATGTTTGTCT[A/G]TTAGCATATCTTCTA | 286053 |
rs372132000 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167528 | AAATTAGCTGGGTTC[A/G]GGAGGCTGAGGCACG | 286053 |
rs372138507 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354880 | CCCACAATGCTCCAA[A/T]ATCCAAAACTTTTTG | 286053 |
rs372201336 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169533 | CAGAAATCTGTTGTC[A/G]TCCTTACTTCCCCTA | 286053 |
rs372204793 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200542 | TTCTGCTGAGAGATC[C/T]GCTGTTAGTCTGATG | 286053 |
rs372208705 | snp | C/G | 0.000153988 | 0.00877328 | splice-acceptor-variant | NSMCE2 | GRCh38.p7 | 8:125102316 | GTGTTTGAAAACTTA[C/G]GTACTAATTTCAAGA | 286053 |
rs372210772 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112500 | CCTGAGTGTCTATCA[A/G]TGGATGAATGCATAA | 286053 |
rs372219016 | snp | C/T | | | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102033 | TTAAGAACTGTGCTA[C/T]TGTTGACTTCTTCAC | 286053 |
rs372264044 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324275 | CTTTAAAAGTTAAAC[A/G]TATATGACCTAGGCA | 286053 |
rs372283613 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235994 | CCTGGAAATATGGCA[-/G]GTTAGGTTATTTGAA | 286053 |
rs372300605 | snp | C/T | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196179 | ATCAGCCACCAAGTG[C/T]AGCCCTGGATAACTT | 286053 |
rs372312434 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304952 | AAGGAAGGAAGGAAG[A/G]AAGGAAGAAAGAAAG | 286053 |
rs372314711 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146548 | TGGCACATATACACC[A/G]TGGAATACTATGCAG | 286053 |
rs372324503 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161369 | TTATCTTGGGTTAGA[-/A]GTAATGCAGTCAGTT | 286053 |
rs372325188 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359336 | GCTCTTTCTCTTTTT[C/T]TTTTTTTTTTTTTTG | 286053 |
rs372333169 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252067 | ATGTCATCTGGAGAT[A/G]GTTGAATCCTTGTAA | 286053 |
rs372437654 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108487 | ACTCTGTCATAAGTT[A/C]TGTAACTTTGAGTAA | 286053 |
rs372438681 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290088 | ATGGGGAACTTCTAG[A/G]CAAGCACCTGAGAAG | 286053 |
rs372461053 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256664 | GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 286053 |
rs372469006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115353 | GGGCTTTAAAAGTAA[C/T]AAAGCCTATATATTG | 286053 |
rs372482344 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235682 | GTGTTTAAATATACC[-/T]TTTTATTTCCTCAAA | 286053 |
rs372553555 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180222 | TATATTGCCTTTCTA[G/T]CTTCTCTTTTCCAAA | 286053 |
rs372579818 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340018 | TTTTTTTTTGTTTTT[G/T]TTTTTTTTTTTTTTG | 286053 |
rs372582380 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248894 | AGAGCCAGCAGCCAG[A/G]CACGGTGGCTCATGC | 286053 |
rs372592587 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265826 | TTAGTTGTTTTTTAA[A/G]TTTTCTCAGACTTGT | 286053 |
rs372601552 | snp | C/G | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093308 | CTCCTAATACCATCA[C/G]CTTGGAAGTTAGGAT | 286053 |
rs372611614 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109855 | TTTCTCTAAATTTGT[C/T]GATATTCTAGTATTA | 286053 |
rs372644459 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157692 | TTCGAAGTAACATAG[C/T]TGCTAATAGGTGAAG | 286053 |
rs372656847 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230016 | AAAACACTAAAACGA[C/T]TTTAGTTTTAATTTT | 286053 |
rs372677563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142990 | GGAGAAGTAACCAAG[C/T]TTCTATTAAATATTG | 286053 |
rs372680856 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178856 | GGCAACAGAGTGAGA[C/T]TCCGCCTCAAAAAAA | 286053 |
rs372701477 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272045 | TTGAGACGGAGTCTC[A/G]CTCTGTCACCTGGGC | 286053 |
rs372704621 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177537 | TCTGATAATTTACTC[A/G]TTCACCCACATCATC | 286053 |
rs372716713 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197720 | TAGTTTTTTCCAATT[A/C]TTTGAAGAAAGTCAT | 286053 |
rs372728291 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176562 | GTGGGTGTCTTTATG[A/T]CAGTCTTGATGAGCT | 286053 |
rs372732907 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211290 | GAAACAGTTACTCTT[A/C]CCAGTTCCTTACATA | 286053 |
rs372733737 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353620 | ACGGGTGCAGTGGCT[C/T]ACGCCTGTAATCCCA | 286053 |
rs372734598 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147098 | TTGCAGAAGTGTTGT[A/G]CAGCAATGCTTTTCT | 286053 |
rs372752459 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135477 | ACCCAAGTTCCCAAA[G/T]ATTTTCTTCTGTATT | 286053 |
rs372790815 | in-del | -/ATATATGTGCATATTCTTTTATAAGTTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326612 | AATTTTTTGAAAACC[-/ATATATGTGCATATTCTTTTATAAGTTT]AAAAAAAAGATTGGT | 286053 |
rs372794791 | snp | C/T | 1.662e-05 | 0.00288266 | utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125366909 | ACCTGCCTGCAGGGA[C/T]ACCAGCAGCCTACCT | 286053 |
rs372795792 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344742 | AGCAAGACTTCATCT[A/C]AAAAAAAAAAAAAGA | 286053 |
rs372814144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119690 | AGGATTATTTTTGAG[A/G]CATCAGATTCCTTTT | 286053 |
rs372847028 | in-del | -/TCTTTATTTCCTTCTTTCCTTCTTTCCTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316633 | TTTCCTTCTTTCCTT[lengthTooLong]CCTTCCTTCTTTCCT | 286053 |
rs372894795 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348914 | CAACATGGCCCAACC[A/C]AACAGCTGGCAGTCA | 286053 |
rs372900279 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151017 | TTTTTTATTTTTTTT[A/T]TTTTTTATTTTTTTG | 286053 |
rs372926740 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340175 | GCCCGCCATCACGCC[C/T]GGCTAATTTTTTTTT | 286053 |
rs372935336 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321035 | CAAGAACTCTATCAT[A/G]AGAACAGCACCAGGG | 286053 |
rs372940266 | in-del | -/TTCC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158714 | GTCAATTTAACTTCC[-/TTCC]AACCTCACAATTTTC | 286053 |
rs372952705 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347781 | GTGGATTGAGTTGCA[C/T]TGGGTTAGATTGGAT | 286053 |
rs372965489 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258461 | CATTCACCCCCGCTC[-/A]CCCCCACCCCACTTT | 286053 |
rs372967403 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291289 | TCATCATTTTAACAC[A/G]TAAAAAACTAGTTTA | 286053 |
rs372973808 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188106 | TTTTAAGCACACCCA[A/G]TCTAGATCTCAAAAC | 286053 |
rs372986112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156782 | TTATCTCAGCTCTCT[C/T]ATTATGCAACTAGTT | 286053 |
rs372995415 | snp | C/T | 4.95749e-05 | 0.00497845 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102519 | CCTCTTTTGTGTCTA[C/T]TTTGAGGTAACACTG | 286053 |
rs372995499 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099284 | ATTGGGAGGGCTTGC[C/T]GTTGTATATCAGATG | 286053 |
rs372997453 | snp | C/T | 3.29462e-05 | 0.00405857 | synonymous-codon, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102438 | AGCCTGTATCAACTC[C/T]GGTATGGACACAGCT | 286053 |
rs373008952 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201499 | CTGGGTATCACCAGC[A/G]GAGGCTGCAGAATCA | 286053 |
rs373020807 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153568 | CAGCAGCTTGGGAGG[A/G]GCCGGGATAATATAC | 286053 |
rs373038631 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327299 | AAAGAGAGAGAAACC[-/A]AAATTGGGAACTATA | 286053 |
rs373043739 | in-del | -/G | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091574 | GGGAGGGGAAGGGGG[-/G]CCATGCAAAAATGGG | 286053 |
rs373044938 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271729 | GTTCTGGAGGATGCA[C/T]GCTTGATTTTATTGC | 286053 |
rs373056191 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307297 | GAGCAGTCTGGGAAG[A/G]TAGCTGAAAGCATGG | 286053 |
rs373087319 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304895 | TCTGAAAAAAAAAAA[-/A]GAGAGAGAAAGAAAG | 286053 |
rs373092069 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137629 | TGTTTTCTGATCTAA[C/G]ATGCATAAATCTTAA | 286053 |
rs373108532 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320981 | GCCAGAGCAGGAGGA[A/G]GAGAGAGGGGCTACG | 286053 |
rs373114865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322235 | TAGCCAGGTGTGGTG[A/G]TGGGTACCTCTAGGT | 286053 |
rs373159805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274125 | TTTCTACTCTGCACC[A/C]ACTCTCCACTCACTC | 286053 |
rs373161335 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324196 | ATCATACCATGTGTT[A/G]GCAAGTCTAGGCAGA | 286053 |
rs373162121 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292221 | AGAAGCTATGGGAGG[A/G]AAAAAAAAAAAGGAG | 286053 |
rs373200498 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225561 | CCCCTGAGAAAGTTC[A/G]AAGTCTAAGGGTACA | 286053 |
rs373240638 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346518 | GTAAATAATGGAAAA[C/T]TGTAGACCTTCTCAA | 286053 |
rs373246900 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138489 | CCTTGGCTTCTCAAA[A/G]TGCTGGGATTACAGA | 286053 |
rs373287592 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218021 | TGTCATATGAGCCTC[C/T]TGATAATTTGTTTAT | 286053 |
rs373321369 | in-del | -/TCCTGCCTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094047 | GGCCTCAAGCAATCT[-/TCCTGCCTT]GCCCTTTCAAAGTGC | 286053 |
rs373339988 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339568 | GCTCCTATTCCCTAG[C/T]GTATCATAATGGACA | 286053 |
rs373383598 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262588 | GGTAGCAAGAATAAA[-/T]TAAGACAGTCAGAGC | 286053 |
rs373407622 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318748 | TGGAAAGGCAATGAT[C/T]CTTGAAGACAGGAAA | 286053 |
rs373420876 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303027 | CGCATCTTCTGTTTC[A/G]CAAGCGGAGAGTCCT | 286053 |
rs373422880 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345522 | TGAGAACATGAAGCT[A/G]AATCAGACAGTTCCT | 286053 |
rs373424285 | snp | C/T | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362418 | ACAAAATGTCGTTAG[C/T]ACCCCATGTCATGCC | 286053 |
rs373438022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268186 | CTGCGGTGAACCATG[A/T]TCACACCACTGCACT | 286053 |
rs373452171 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317078 | CAGGCTGGCTCACCA[C/G]TCCTGGCCTATTGTT | 286053 |
rs373464384 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289113 | CAGTCTTTAATTCAT[C/G]TTTGTACTTCCAAGG | 286053 |
rs373473352 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131731 | ATATTTTAAAAATGC[A/C]AAATTGGAGCTTCTG | 286053 |
rs373505825 | in-del | -/TATT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212703 | ATAATCTAAATAATT[-/TATT]AAGATAACATTTTTT | 286053 |
rs373523780 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323017 | TGAGCCAAGATCATG[C/T]TGCTACACTCCAGCC | 286053 |
rs373525816 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161791 | AGTGAGACAATGTCT[A/C]AAAAAAAAAAAAAAA | 286053 |
rs373531913 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341992 | GATAATTATGAATGA[C/T]GTGTTTGATATGTTA | 286053 |
rs373535867 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197771 | CATTGAATCTATAAA[C/T]TACTTTGGGCAGTAT | 286053 |
rs373537282 | in-del | -/ACC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278777 | AAATTCACTTCCACC[-/ACC]TGTTCAAAAATTGCT | 286053 |
rs373537439 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338435 | CTTTTGAAAAGCTTT[C/G]TTCCTTTTGCACCTT | 286053 |
rs373578805 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137353 | AGGGCTGATTTGTTT[A/T]ATTAAACTGTTCCTT | 286053 |
rs373581438 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278416 | ACAGAAGCCCCAAGG[A/G]CAGTATGCTAGTGCA | 286053 |
rs373612467 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323295 | TTTGTAGATATTGAC[A/G]AGATTATTCTGAAAT | 286053 |
rs373625164 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110762 | ATTTTGGTTGTTGTT[-/G]TTTTTTTTTTTTTTT | 286053 |
rs373630474 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175865 | TTTGTGTTAAAATAT[A/G]GTGAAAATAATATGT | 286053 |
rs373651645 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129355 | GAAAGGATACTTAAA[-/CA]TCTTTTTAAGCCTAT | 286053 |
rs373659410 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297191 | TTAGTCAAGGTAAAT[C/G]TCTGAATATAATGTA | 286053 |
rs373681301 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237757 | GAGTCTGCAAGGCTT[A/G]TCAGGGTAAATACTA | 286053 |
rs373683399 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254350 | ATGGTGCGTCATCAA[A/C]TAGTTGAATTACAAT | 286053 |
rs373690774 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320030 | AAAATATAAAAATTA[A/G]CTGGACGTGGTGGCA | 286053 |
rs373696336 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350251 | GATAGAGAAAGTCTG[G/T]GTGGCTTCTTTAGCT | 286053 |
rs373711332 | in-del | -/GGTGGGGTGGT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301473 | CTACATGGAGGTGGC[-/GGTGGGGTGGT]GGTGAGGATTAAGTG | 286053 |
rs373716180 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093987 | TTTTTTTTTTTTTGT[A/T]GAGTTGGGGTCTTGC | 286053 |
rs373738008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235081 | TGAAAACCCACCTCT[A/G]CTAAAAATACAAAAA | 286053 |
rs373742362 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183194 | CTTAATGTAGGGATT[C/T]GTATTTTGAAATAGG | 286053 |
rs373755146 | in-del | -/A | 0.189576 | 0.242588 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216208 | ACATTTTGTTGATCC[-/A]ACTTATCTGTCAATG | 286053 |
rs373780389 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232190 | ACATGGAGAAATCCC[A/G]TCTGTACTAAAAATA | 286053 |
rs373821452 | in-del | -/ATTA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325102 | CATAGTTAATTATAT[-/ATTA]ATTATGCCTCATTAA | 286053 |
rs373880176 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257141 | ATACAAAAATTAGTC[A/G]GGCGTGGTGGCACGT | 286053 |
rs373882003 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266999 | TAACTTTTCTTTTTT[C/T]TTTCTTTTTTTTTTT | 286053 |
rs373891872 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352432 | AGTGAGCCGAGATCA[C/T]GCCATTGCACTCTAG | 286053 |
rs373895731 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337663 | ATGTTGGGAAGCCGA[A/G]GCTGGCGGATCACCT | 286053 |
rs373906029 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304104 | CAGGATAAAGTCAAA[C/T]GTGGCTGTGAATTTC | 286053 |
rs373906204 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327714 | TTTAGAATATTACAG[A/G]ACTTGAAGGTTTGAC | 286053 |
rs373914591 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257824 | CAGGCGTGAGCCACC[A/G]TGCCCGGCCAGACAA | 286053 |
rs373937145 | snp | C/G/T | 3.32492e-05 | 0.00407722 | missense | NSMCE2 | GRCh38.p7 | 8:125182185 | TACAGAGCAAGAATT[C/G/T]TGATGCAGACTTTCA | 286053 |
rs373939479 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316112 | ACACCTGGTCTAAAC[C/T]TCATTCTTATCAATG | 286053 |
rs374005320 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268565 | TATTCCTTAGGTTGT[G/T]GGGGATGCAGACCTG | 286053 |
rs374006202 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262715 | TTTTTCTAAAAACTC[A/G]CTGGTAGGCTGTGTG | 286053 |
rs374051840 | snp | C/T | 0.209693 | 0.246729 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316713 | CCTTCCTTCCTTCTT[C/T]CCTTCTTTCTTTCCT | 286053 |
rs374055746 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223717 | AATTTGCATTTCCCA[C/G]GTGTCTGGAGAAGTT | 286053 |
rs374058692 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309016 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACCTGAG | 286053 |
rs374072770 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205492 | TCTGCTGCTTTTGGT[A/G]ATGGTGCATCCCAGG | 286053 |
rs374077037 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212909 | TAATTCAAATATTTG[A/G]GGTAGGCAAGTAGAG | 286053 |
rs374081089 | in-del | -/T | 0.212293 | 0.24714 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254606 | TCTGTTTACCTCAGA[-/T]TTTTTTTTTTTAATA | 286053 |
rs374081931 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194442 | TTTGTTGCATTCTAT[A/T]GCTGAGTAGTATCTC | 286053 |
rs374091684 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122021 | AGTTCTTACCTACGC[A/G]TTATTGACCTAGGCC | 286053 |
rs374119758 | snp | A/C/T | 0.00010352 | 0.00719379 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357177 | CTTCCTTTTCTTTGA[A/C/T]GTTAGACCAGAGAGG | 286053 |
rs374125244 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119176 | CTCCTGTTACCGTGG[A/G]ATCTCACTCCATAAA | 286053 |
rs374129324 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111402 | AATTTGGTAAGTATG[A/G]GTGAAAAAAAACTCC | 286053 |
rs374131070 | snp | A/G | 0.000132503 | 0.00813842 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357335 | GTACCGCTTCCTCCT[A/G]CTTCCCCTGAAAGAA | 286053 |
rs374178645 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298587 | CACTTTTGTTTCCTT[A/G]TCTGTAAAAACAGGC | 286053 |
rs374204554 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259646 | GTTGTGGAACAGCAA[C/T]ATCTTACCCTGTGGC | 286053 |
rs374208917 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177640 | GAGCCATAATTCCAG[C/T]GCTGTGTGCAGAATG | 286053 |
rs374279014 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260294 | TAGCCCAGTATAAAA[A/G]TGTGTTTTTCAGAAT | 286053 |
rs374295431 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230659 | CTAATCGTATGCCAA[C/T]GAGGAAAAACACCTT | 286053 |
rs374301234 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138400 | CTGGCTGATTTTTTT[A/G]TTTTTAGTAGAGGTG | 286053 |
rs374301507 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334772 | TATGAAGTATCTTTT[C/T]TTTTTTTTTTTTTTT | 286053 |
rs374316374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201995 | TAGCAGTGAGCAAGG[C/T]TCCGTCGGCATGGGA | 286053 |
rs374321892 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190537 | GGACCAAATAAATAA[G/T]TAAGAAAAAGATTAA | 286053 |
rs374325825 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156340 | ATGTGCTGCTTCTGG[A/G]TGTTAATTTATTGAA | 286053 |
rs374349288 | snp | G/T | 6.59217e-05 | 0.00574078 | missense | NSMCE2 | GRCh38.p7 | 8:125357265 | AACAGAAGGAGTGGA[G/T]GAAGATATAATTGTG | 286053 |
rs374381391 | snp | C/T | 1.64798e-05 | 0.00287047 | missense | NSMCE2 | GRCh38.p7 | 8:125151225 | TTGAATTTGCTACAT[C/T]GGATCGGCAACTAAA | 286053 |
rs374425521 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106739 | TGTGGCTCACACTTG[G/T]AATCCTAGCACTTTA | 286053 |
rs374428480 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316731 | TTCTTTCTTTCCTTC[-/T]TTTCCTTCCTTCCTT | 286053 |
rs374435320 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172043 | CCTACATTAATTCAT[A/T]TAATACTCAAAGGTT | 286053 |
rs374436188 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183951 | TGAACTAATATATGT[A/G]CCAGTTATTAACATC | 286053 |
rs374436335 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159246 | AATTTATAAATTAAA[C/T]GTTATTGTAGGTATG | 286053 |
rs374441495 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133476 | CGGGTGTGGTGGCTC[A/C]TGCCTGCAATCCTGA | 286053 |
rs374466058 | in-del | -/CA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118407 | AAACACACACACACA[-/CA]GAGATTGCTGGACCT | 286053 |
rs374485748 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104758 | ACTGCTGTGCTAGGC[C/T]GAGCATGGTGGCTCC | 286053 |
rs374488808 | in-del | -/GAAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313214 | AGAGAAAGAAAGAAA[-/GAAA]AGAAAGAAAAAGAAG | 286053 |
rs374525814 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347087 | ACAGCTTGCTATTTG[C/T]CAGGAACCATGCTAA | 286053 |
rs374551109 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306195 | ATTAGCCAGGTGTCA[G/T]GGCATGTGCCTGTAA | 286053 |
rs374557893 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120839 | CAAGTCGCAAGAGGC[A/G]CATTCCTTGCATGAA | 286053 |
rs374561539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258840 | TGACATTTCCTTGGT[A/T]CAAGACATTGTGGTC | 286053 |
rs374575948 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091854 | CTGATGACGCAAGAG[C/T]CCGCTCTCACTTTTC | 286053 |
rs374606635 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336248 | TTTATTATGTGCTGG[-/G]CATATTAAATAATCA | 286053 |
rs374613919 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302635 | ACTTCTTAATCAGAT[A/G]GAACAAGAAGATTAG | 286053 |
rs374618803 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225738 | AGCAAATTATACTTA[C/T]TTGCTGAACAAAGCA | 286053 |
rs374621338 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164894 | TATTCAGTTATCTCC[A/G]GTTGAATAATTGTTT | 286053 |
rs374624234 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216405 | AGCACTTTGGAAGGC[C/T]GAGGCAGGCAGATTA | 286053 |
rs374625317 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139480 | GGAAAGAGGTTTAAT[G/T]GACTCACAGTTCCAC | 286053 |
rs374656766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364895 | AGCAAGTAGGTGGTA[C/G]AGAGAAAATTCAGAC | 286053 |
rs374659262 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302718 | GGGTTGGGGAGCGTG[C/G]AGGGGCAGTATTCAA | 286053 |
rs374666424 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348569 | ACGTGTTGTGAGAGG[G/T]CCCCAGTGGGAGATA | 286053 |
rs374688471 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314065 | TAATCAAATAGGATA[A/G]CAAACGTGCAGAGAT | 286053 |
rs374694989 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333648 | GCCTCCCAAGTAGCT[A/G]GGACTACAGGCGCCC | 286053 |
rs374706377 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289664 | ATGAATAATGAAGGA[A/G]TATACTTTAAAAGTA | 286053 |
rs374710129 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149309 | GAAATATACTTATAA[A/C/G]TAACTATTATAAAAT | 286053 |
rs374711405 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366495 | CAGTGAGCCAGGATC[A/C/G]TGCCACTGCACTCCA | 286053 |
rs374711996 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244657 | GCTACTGTTGAATTA[G/T]AGGCAAAAGTATTAT | 286053 |
rs374732149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259188 | AGCCACTGTACCTGG[A/C]CTACTCACAGAGCTT | 286053 |
rs374743194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223093 | AAAATAAAATAAGCA[C/T]GGTGGCTCACACCTG | 286053 |
rs374745146 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118208 | AAAATTAGCTGGGCA[-/T]GGTGGCACACGCCTC | 286053 |
rs374755345 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201930 | TCCCCCACCCCATTC[C/T]CCCGCCTTCCTGCGA | 286053 |
rs374762244 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185519 | CCATGTTGGCCAGGC[C/T]GGTCTTGAACTCCTG | 286053 |
rs374767077 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112068 | TTCTAGTGGTGAGTG[A/G]TGGCCACAATGATAA | 286053 |
rs374809693 | in-del | -/TTTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316731 | TTCTTTCTTTCCTTC[-/TTTT]CCTTCCTTCCTTCCT | 286053 |
rs374815530 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151024 | TTTTTTTATTTTTTA[-/T]TTTTTTTGAGGAGGT | 286053 |
rs374821404 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322351 | GCAGTCTGAGAGTGA[A/G]TGAAGCAGAAAGAAG | 286053 |
rs374832644 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296678 | TGGGATTACAGATGT[A/G]AGTCACCGCACCCGG | 286053 |
rs374838217 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253878 | CTTGGTAAAATGCTA[C/T]CACATATGCAGTTAA | 286053 |
rs374845167 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140808 | CTTGAGCACAGCCAA[A/G]GACTTGAAGACCAGA | 286053 |
rs374861151 | in-del | -/AA | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363541 | AAGAAAGAAAGAAAG[-/AA]AGAGAGAGAGAGAGA | 286053 |
rs374877416 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305466 | AGAGGCTGAAGAGAA[A/G]TCTTAGTTCTGGAAG | 286053 |
rs374883759 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292564 | TCTCAAAAAAAAAAA[-/A]GAACCTATGGGAAAC | 286053 |
rs374896631 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252271 | CAGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 286053 |
rs374908708 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344534 | AATCACCTGAGGTCA[A/G]GAGTTTGAGACCAGC | 286053 |
rs374909390 | in-del | -/CCTACTC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179797 | TCACTGCCCCCACTC[-/CCTACTC]AGTCTTCACCTCCTC | 286053 |
rs374918920 | snp | C/T | 1.66313e-05 | 0.00288364 | utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125366912 | TGCCTGCAGGGACAC[C/T]AGCAGCCTACCTCCT | 286053 |
rs374920309 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146319 | GAGTGGGAGGCCTGG[C/T]GCTGCTGCTAACTAC | 286053 |
rs374925530 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117148 | TGTATACAGTGGACT[C/T]GCAGTGGTGTCTATT | 286053 |
rs374929626 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296372 | GATTTGGCTGTAGTC[A/T]AATTGTTGTTGCCAT | 286053 |
rs374934126 | in-del | -/TA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272756 | ATATATATACACACG[-/TA]TATATATATACACAC | 286053 |
rs374950730 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238966 | TTAATGATATGGGGC[C/T]GAATTGTTATTCAAA | 286053 |
rs374957855 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262976 | TTCTCTTGAACTAGA[C/T]CTATATGTTTATGCT | 286053 |
rs374992683 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291704 | TGTTTTTCTGGAGTT[A/T]TATTAGTATTTTTGT | 286053 |
rs374996419 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102448 | AACTCTGGTATGGAC[A/G]CAGCTTCTAGTGTTG | 286053 |
rs374997022 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337501 | CATCACTTGAAATCC[G/T]AATTTTATTTGCCAG | 286053 |
rs375008651 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212025 | AAACGTTTATGGATT[A/G]ATTAGCCTAAGTGGG | 286053 |
rs375043269 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199311 | TGCTTTCTCTTATGG[G/T]CATCTAGTGCTATAA | 286053 |
rs375152642 | snp | A/T | 0.189576 | 0.242588 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216212 | TTTTGTTGATCCACT[A/T]ATCTGTCAATGGACA | 286053 |
rs375173552 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301234 | CCTGAGGAAAATCAC[A/C]TGCCTGTACAGTCGG | 286053 |
rs375199753 | in-del | -/AGAA | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363624 | GGGGGAGGGAAGGAA[-/AGAA]GGAAGGAAGAAGAGA | 286053 |
rs375202531 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127705 | TGAGGGGTTTGGAGT[C/T]TTGGCTGAAACTTAA | 286053 |
rs375206345 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267105 | TACCTCCTGGGTTCA[A/T]GCAATTCTCTTGCCT | 286053 |
rs375208307 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317439 | AGAGCTCAATTGATC[C/T]ACCCGCCTTGGCCTC | 286053 |
rs375210742 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261759 | GTAAAAAAAAAAAAA[A/C]AAAAACAAAACAGCT | 286053 |
rs375241876 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298442 | ACCCAGCCAGTAAAC[A/G]TGAGATCCAGCGTTT | 286053 |
rs375253079 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167084 | CATGTACTCTCACAC[A/G]AAGACTGGAGCAAGG | 286053 |
rs375254319 | snp | A/C | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129071 | GTGGGGATGACAAAT[A/C]AACAGTTGGTTTTTG | 286053 |
rs375257341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275437 | TTATTCTTCCCTGTA[C/T]CCTCCCATGGTATCC | 286053 |
rs375267223 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291435 | ACTCTTAGCCTGGAG[-/C]TCGATGTAATTATAT | 286053 |
rs375267630 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108099 | CCCTGAAAGGGCCCA[A/G]AAGAAATTACGATGA | 286053 |
rs375340482 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282885 | TGAAAATATTTTTAC[C/T]GAAATTATGGATGGA | 286053 |
rs375369058 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101252 | GACTAATAATGGAGA[A/G]ACTACAATAGTAGTT | 286053 |
rs375400013 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145073 | ATATTAGAGCACTTC[A/C]CTCTAAAAAGAAACC | 286053 |
rs375400872 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144407 | GAATCTTCTGCTCTC[C/T]TATCTGCTGTTGCTT | 286053 |
rs375402267 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178739 | GCCGGGCATGGTGAC[A/G]GGCACCTGTAGTCCC | 286053 |
rs375458842 | in-del | -/CTAA | 0.0111196 | 0.0737302 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175981 | GAGCCATTTGGAGCC[-/CTAA]CTTAGTTCCTAACAG | 286053 |
rs375490329 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309131 | GCATCCCTGTAATAC[C/T]ACCTACTCAGGAGGC | 286053 |
rs375498540 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298073 | AAGACCAGCCTGGCC[-/G]AACATGGTGAAACCC | 286053 |
rs375499011 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280829 | AAGATTCAAAGTTTG[A/G]TAAGGGAAATCTCAT | 286053 |
rs375501938 | snp | C/T | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092012 | AGGAGTTTCGCCACC[C/T]TCAGGGACACTCCAC | 286053 |
rs375512845 | in-del | -/TTAT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213741 | TCCTTCCTTCCTTCC[-/TTAT]TTCCTTCAACTGTAC | 286053 |
rs375529741 | snp | C/T | 3.29696e-05 | 0.00406001 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102340 | TTCAAGATGCCAGGA[C/T]GTTCCAGTTCAAATT | 286053 |
rs375536009 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272149 | CTCCCGAGTAGCTGG[A/G]ACTACAGGCGCCCAC | 286053 |
rs375548829 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161623 | GCCAACATGGTGAAA[C/T]GCCACCTCTACTAAA | 286053 |
rs375575657 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143462 | GCCAAAATGGACATA[C/T]GTACTTTATGACATT | 286053 |
rs375601260 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317619 | CAAAGACAGTTGCCT[A/G]TCTGAAGTCTAGGTC | 286053 |
rs375617254 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249455 | ATGGGGAGTGTTCGG[G/T]ACTCAAGTTTCATTC | 286053 |
rs375623007 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150810 | CAGATATAAGACAGA[A/G]CTGCTTAATGGATGA | 286053 |
rs375627209 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171926 | CTCTTGAGCACTTGG[C/T]AGTGTGACCGAGGAA | 286053 |
rs375668382 | in-del | -/AAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136699 | TTATTCCCATTATAG[-/AAG]TAGTTTACTTCACTC | 286053 |
rs375690500 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257291 | CCATCTCAAAAAAGA[-/A]AAAAAAAAAAAAGAC | 286053 |
rs375697705 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241389 | TAATACAGAATACAT[-/T]CAATAATAGTGGAAG | 286053 |
rs375698036 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234035 | AAAAAAAAAAAAAAA[-/T]ACAAAAAATTAGTCG | 286053 |
rs375700538 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164454 | GTCTTGGTTATAAAG[C/T]ATATTTATGATTTTG | 286053 |
rs375705941 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119827 | ATTATCCAGACCTAT[G/T]TTTTCTCCCTCTTCT | 286053 |
rs375714497 | snp | A/G | 0.00172388 | 0.0293082 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357666 | AAACAGCTACTGGAA[A/G]TTGATCATTATCATT | 286053 |
rs375750940 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278607 | GATGATATGGTAGAG[A/G]TGTTTCCTCAGCAAT | 286053 |
rs375774620 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180478 | TGCATAGCAATTAAG[A/C]AAAAGAAGATTATGT | 286053 |
rs375799206 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312959 | CATATCACATGCAAA[A/G]GCCCTGGGGCTAGAG | 286053 |
rs375831748 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192344 | TTTTTTTTTTTTTTT[-/T]AAAGAAAGTTTAAGT | 286053 |
rs375833656 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316709 | TTTCCTTCCTTCCTT[-/C]CTTTCCTTCTTTCTT | 286053 |
rs375838969 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220791 | AATTTTCTTCCTAGT[A/G]AGATCTGAGATCGAT | 286053 |
rs375842251 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174475 | ATCATTCCGGTTGGT[C/T]ATCGTATTATAGTGG | 286053 |
rs375865994 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260136 | AGAGCTGGAACACAC[C/G]CTACTACACGACTCT | 286053 |
rs375887995 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102180 | TGGTGTCTTCTCTAT[A/G]GGATATACAGAATAG | 286053 |
rs375892728 | snp | A/G | 1.69746e-05 | 0.00291325 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357831 | CTAGTGAGTGGACGC[A/G]GGGAAGGAAGTGGAG | 286053 |
rs375934019 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154697 | AGTTCTATATGAACT[C/T]TTTTGATATTTTCAG | 286053 |
rs375939883 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257148 | AATTAGTCAGGCGTG[A/G]TGGCACGTGCCTGTA | 286053 |
rs375945304 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171605 | TTGAGAGCAGCTGCT[A/G]CTACTAATACTGCTG | 286053 |
rs375948450 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143744 | GCCGTGGGCAAAACT[A/G]TACAGTTGAATCAGA | 286053 |
rs375954530 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253771 | TTTAAAAGATAATTA[C/T]TATTCCATTTCCTAA | 286053 |
rs375967233 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151555 | TTTGAATGTGAGGAG[A/G]TTTTTATAAAATCCT | 286053 |
rs375972265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312028 | AGCAGAGATCAGGTC[A/G]TTATTGCACTCCAGC | 286053 |
rs376020030 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358428 | TCTTTATAAATAGAC[A/T]TAATATATATTATAT | 286053 |
rs376040362 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258335 | AGCTCACAAGAGGCA[A/G]GAAGGATTGATAGGT | 286053 |
rs376045445 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204661 | AGGGGTTTTACTTTA[C/T]ATTTACCAAAAGCAG | 286053 |
rs376050058 | snp | C/T | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367493 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGCCTC | 286053 |
rs376058106 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291416 | TCCATTTTTAAATTG[G/T]TAAACTCTTAGCCTG | 286053 |
rs376083391 | in-del | -/TAC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234035 | AAAAAAAAAAAAAAA[-/TAC]AAAAAATTAGTCGGG | 286053 |
rs376142167 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143256 | TGATACTGTGATTTG[-/T]TTTATTTTATCCAAA | 286053 |
rs376175651 | snp | A/G | 0.000314499 | 0.012536 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151328 | TACAACTCACTGACC[A/G]AGAAGTAGAAACACA | 286053 |
rs376175909 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189232 | TGGAATAATGACAAG[A/G]GCACACCTGAACAAA | 286053 |
rs376192964 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213745 | TTCCTTCCTTCCTTC[C/T]TTCAACTGTACAGAG | 286053 |
rs376203060 | snp | C/T | 1.7586e-05 | 0.00296524 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182060 | CTTTGTTAACACTAT[C/T]ATTATTAACATTTAA | 286053 |
rs376240525 | in-del | -/TC/TCTC/TCTCTCTC | 0.0420344 | 0.139882 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124470 | GGATTCCTCAGGATT[-/TC/TCTC/TCTCTCTC]TCTCTCTCTCTCTCT | 286053 |
rs376249914 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134407 | GGGAACTCTATAGTC[A/G]CTCCCCATCCTTGTC | 286053 |
rs376265171 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166378 | TTCAAGAGATTCTTG[-/C]GCCTCAGCCTCCCAA | 286053 |
rs376294406 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318757 | AATGATCCTTGAAGA[C/T]AGGAAACAAAGGAAA | 286053 |
rs376302579 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338632 | AGTTAGCAATTACAG[C/G]TAACATCATGCAAGA | 286053 |
rs376316148 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343874 | AGCTGGACGTGGTGG[C/G]GGGCGCCTGTAGTCC | 286053 |
rs376328604 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217774 | GTACTTAGTGTGGCT[-/G]GTTTTCCAGACTTGA | 286053 |
rs376336763 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359191 | AGAATGGCATGAACC[C/T]GGGAGGCGGAGCTTG | 286053 |
rs376355063 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271868 | GAATTCAGCAATATT[A/C]AATAATCTGCATAAT | 286053 |
rs376378392 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339816 | GTCACACTATGCTAC[A/C]GTCGTGGGTTTCCTT | 286053 |
rs376378855 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221559 | AGATGTGTCTTATCC[A/G]TAGACATATTATAGG | 286053 |
rs376406130 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139651 | ACAAGAACAGCACAG[A/G]AAAGACCTGCCCCCA | 286053 |
rs376450700 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265567 | CGTTAAAATGCTGCT[A/G]TCTTTATTCAGTTTT | 286053 |
rs376453934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182362 | GCTTATCTGCTTGGC[C/T]TGATCCTCATTCTAA | 286053 |
rs376465845 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271746 | CTTGATTTTATTGCT[A/T]TTGATACTGTTTTTC | 286053 |
rs376487105 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342028 | CTCAGGTGGTGGGGG[G/T]GTTAAGGGGAGACTC | 286053 |
rs376515182 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170557 | GATTTACAGGCATGT[A/G]CCACCATGCCCGACT | 286053 |
rs376517090 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257153 | GTCAGGCGTGGTGGC[A/G]CGTGCCTGTAATCCC | 286053 |
rs376628819 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150452 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCACT | 286053 |
rs376641588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297411 | CTCCTGGGACAGGCA[A/G]CTCATTCCATTTTCA | 286053 |
rs376671779 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211273 | GGGCCTCTGCCTCCC[C/T]GGAAACAGTTACTCT | 286053 |
rs376695595 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227976 | ATTGATTTATTCCTC[-/TT]TGAATCATTACCCTC | 286053 |
rs376707085 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309429 | CACTTTACCATAGAA[A/G]TGTTTTATTAAGATC | 286053 |
rs376720891 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111413 | ATGGGTGAAAAAAAA[-/A]CTCCCAGAAAATTGT | 286053 |
rs376721370 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272304 | CAGGCTTGAGCCACC[A/G]CGCCCGGCAAATCTG | 286053 |
rs376747044 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144763 | CCTCATTCATCATCT[C/T]CTATTCATTGAAGTC | 286053 |
rs376771234 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333584 | CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC | 286053 |
rs376788258 | in-del | -/CT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254201 | CTCTATTGAAACACT[-/CT]GTGTTTCAGTCGTGT | 286053 |
rs376798358 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130834 | TGATTTGTAATTTCC[C/T]TCACCAACATTAAGA | 286053 |
rs376800710 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268241 | GCTGTCTCAAGGAAG[-/A]AAAAAAAAAAGTATT | 286053 |
rs376835701 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250531 | ACAACCTGCTTTTAC[C/T]TGTTTCACTTATATT | 286053 |
rs376847221 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194130 | TTTCACAACAACTTA[A/G]TGTGGTAGGTAGATA | 286053 |
rs376865181 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280406 | TACCTAAAATGTTCT[A/G]TGGTTGCAACATCTG | 286053 |
rs376876097 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235723 | TCAAATTGTTTTATT[C/G]ATACACATCTTATCT | 286053 |
rs376891892 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183547 | TAGTGAATTAATTGT[A/G]TAGCCATGAGAATTA | 286053 |
rs376897321 | in-del | -/TCTC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124471 | GGATTCCTCAGGATT[-/TCTC]TCTCTCTCTCTCTCT | 286053 |
rs376902112 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272656 | ACAATAAAACAGTTA[C/T]AGAAATTGCCTTATT | 286053 |
rs376905384 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119501 | GTTTAGGTTTCAGTG[A/G]CCTAACAGGGTTTGA | 286053 |
rs376923068 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224470 | AATCCATTTTGAGTT[A/C]ATTTTTGCATATATT | 286053 |
rs376923303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258989 | CTCACTGCAACCTCC[A/G]CCTCTTGGGTTCAAG | 286053 |
rs376938663 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122523 | CATATGCTCTTTAAG[C/T]CTCTTTTCTCTGCTC | 286053 |
rs376943652 | in-del | -/CCTTCCTTCCTTCCTTATTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213707 | CTCTTTCCCTCCCTC[-/CCTTCCTTCCTTCCTTATTT]CCTTCCTTCCTTCCT | 286053 |
rs376994069 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313593 | CTTTTGTTGTCACCT[G/T]CCACATAAAGGAGAC | 286053 |
rs376997418 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199058 | TCATTTTTTTATTGC[A/G]TCTGTATGATTCCTC | 286053 |
rs377005100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223328 | GCACCACTGCACTCC[A/G]GCCTGGGCAACAGAG | 286053 |
rs377023324 | in-del | -/AT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202685 | GATATTTTTGAACTT[-/AT]TAGAGGCATTTACTT | 286053 |
rs377087113 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176268 | AGAGTCTCTAGTGAC[C/T]CAAAAATCTAATGCA | 286053 |
rs377094700 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211459 | CTTTTTAATGGCTAT[A/G]TAAAATAGTACTATA | 286053 |
rs377098974 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130501 | TCTGTAAAGAGTTTT[A/G]TTTTCTCTGCTTCTG | 286053 |
rs377104214 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108333 | GTCCAAGGACCCAGA[A/G]AGTAGGAAAACACCG | 286053 |
rs377141887 | in-del | -/TAT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299772 | ATGTAGTTTGAAGAC[-/TAT]TATTACCTTGACCTC | 286053 |
rs377152138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156911 | TATCCACTACTTTAA[C/T]ATGAAATTCTATAGG | 286053 |
rs377152315 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307086 | CAGCTCCCTGTTCAC[C/T]TAACATGGAGGAAAG | 286053 |
rs377179108 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157074 | GACCACTTACTGACT[-/G]AATATAAGAATATAC | 286053 |
rs377203119 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365595 | GCACGGTGGCTCATG[C/T]CTGTAATCCCAGCAC | 286053 |
rs377206037 | in-del | -/GAGGATAATGTTATCTGA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110787 | TTTTTTTTTTTTTTT[-/GAGGATAATGTTATCTGA]TTTTTTTTTTTAAAT | 286053 |
rs377215801 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265611 | CCTCTTAAATTTTGC[C/T]TCTCAGGCAGGTGGC | 286053 |
rs377218004 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295022 | ATTGTGGGCCAATAA[G/T]CTGTCACCTGAAACT | 286053 |
rs377222438 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209372 | TTTAGGGACTAAACC[A/G]GTAGAAATAATTGGG | 286053 |
rs377227797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161554 | TGTAATTCCAGCACT[C/T]TGGGAGGCTGAGGCG | 286053 |
rs377230348 | snp | A/T | 1.72234e-05 | 0.00293452 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357173 | ATTCCTTCCTTTTCT[A/T]TGACGTTAGACCAGA | 286053 |
rs377230784 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136677 | ACACAGATACACTAG[C/T]GGGTGCTTATTCCCA | 286053 |
rs377257796 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324357 | AGACTTCTACTACAC[A/T]AATGTTCATAGCAGC | 286053 |
rs377270342 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273242 | TCAACCAGATACTGA[G/T]ACCATCCCTTGTTCA | 286053 |
rs377274636 | in-del | -/ACCTG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115791 | TATTGTTTAGTCTTG[-/ACCTG]GGAGATGCTTGCTGA | 286053 |
rs377281203 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215558 | TTGGGTATATACCCA[A/G]TAATGGGATGGCTGG | 286053 |
rs377283002 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191430 | AAAAATTGACTTTTA[A/G]TAGGACTCTTGAAGA | 286053 |
rs377285996 | in-del | -/CGG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242108 | AAACAATAACTGGGG[-/CGG]GGGGAGTTTGAGAAC | 286053 |
rs377289373 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142744 | CGAGTAGCTGGAATT[A/G]CAGGCATGCACCACC | 286053 |
rs377295828 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138367 | TAGCTGGGACTTTAC[A/T]GGTGCATGCTACTGT | 286053 |
rs377337253 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218659 | TCAGGTGATCCACCC[G/T]CCTCAGCCTTCCAAA | 286053 |
rs377398075 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094914 | GCTGGAGTGCAGTGG[C/T]GTGATCATGGCTTAC | 286053 |
rs377402385 | in-del | -/AGAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305017 | GAAGGAAAGAAAGAA[-/AGAA]GGAAGGAAAGAAAGA | 286053 |
rs377404819 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303119 | AAAGGCCAAAATACC[A/G]AAGGTTCAGTTTCCT | 286053 |
rs377406386 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173734 | ACTGAAAGTTAGGAT[G/T]TATGTCTGAAATCAT | 286053 |
rs377464765 | in-del | -/CC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345044 | AAAAAAAAAAAAAAA[-/CC]CCTCCACATTTTTGA | 286053 |
rs377467354 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297732 | CATAGCTAGTTGGGA[G/T]GCTGAGGTAGAAGGA | 286053 |
rs377468985 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213749 | TTCCTTCCTTCCTTC[A/C]ACTGTACAGAGACCT | 286053 |
rs377505765 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267003 | TTTTCTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 286053 |
rs377506934 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335433 | GCTCAAAAACACAGA[A/G]GGACTGAGGCAGGCA | 286053 |
rs377517025 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257978 | GAGAGATGGAAAATA[C/T]GTAAATACTTTTATG | 286053 |
rs377527288 | in-del | -/AAA/AAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304960 | AGGAAGGAAGGAAGA[-/AAA/AAG]AAGAAAGAAAAAGGA | 286053 |
rs377535140 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297316 | ATTTTACCCAGTTTT[C/T]CCCCTCCCCTGCAAA | 286053 |
rs377542938 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133162 | ACTGCAGATATCCAC[C/T]AGAGGATGATAATTT | 286053 |
rs377577693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259243 | GCCAGACAGAGATGG[G/T]CTCCTGAGTGAACTC | 286053 |
rs377579713 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346375 | TATACGAACAACTTG[C/G]ATGTACTGTCTTGAG | 286053 |
rs377585366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279620 | AGAAATGCATTAAGA[C/T]AGAAAGGTTGCTACT | 286053 |
rs377586253 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327781 | CCACAAAATATATGT[A/G]TACAATTGTTTTAGG | 286053 |
rs377586716 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304802 | TCAAGCGATGAGAAT[C/T]GCTTGAACCCTGGAG | 286053 |
rs377625744 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091539 | CTCTGCAGACCTCCC[A/C]GTGGCCAGCGCGGCC | 286053 |
rs377639700 | snp | C/T | 1.69e-05 | 0.00290684 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151124 | AACTTTTTCCAGATA[C/T]GGCATTTTAAATGGA | 286053 |
rs377647612 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202026 | CCTGCCAAGCCAGGC[A/C]CAGGAGAGAATCTCC | 286053 |
rs377651048 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181047 | TTTGGTGAGTTTTGC[C/T]TGGCAGCAGGAGCAT | 286053 |
rs377653236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131590 | CCATGGTAGCTTTTC[A/G]TTGAGTTCTAACGTG | 286053 |
rs377655433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098803 | GGTTTGGGGGAGGGG[G/T]AGGGTGGGAGAGAAG | 286053 |
rs377659975 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181701 | CTAGGGTGGAGGGCC[-/A]AAAAAAAAAAAATGT | 286053 |
rs377703235 | snp | A/G | 3.29603e-05 | 0.00405944 | missense | NSMCE2 | GRCh38.p7 | 8:125151231 | TTGCTACATTGGATC[A/G]GCAACTAAACCATTA | 286053 |
rs377715765 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192398 | GGTGTGTTATTGTGT[-/G]TATAGCAAGTAGACA | 286053 |
rs377725636 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114879 | AATACTAAGGGTTCT[G/T]TAGGTAAATAATACT | 286053 |
rs377735162 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320233 | AGGAGGGAGGGAGGG[-/A]AGGGAGGGAGGGAGG | 286053 |
rs377739935 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341587 | TGTTAGTTTTTTTTT[-/T]CCTCTAATGAGGGCA | 286053 |
rs386413919 | in-del | -/TA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272709 | TTGGGATATATATAT[-/TA]ATATATAATATATAT | 286053 |
rs386729613 | multinucleotide-polymorphism | GA/TG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104014 | TTTTTTTTTCAGCCG[GA/TG]ATTTTGCTCTTGTTG | 286053 |
rs386729614 | in-del | AGTGGATCAACAA/CACTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216208 | CACATTTTGTTGATC[AGTGGATCAACAA/CACTT]ATCTGTCAATGGACA | 286053 |
rs386729615 | in-del | AATTG/CA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227567 | TAATTACATCATCTT[AATTG/CA]CAAATGTATTGCAAT | 286053 |
rs386729616 | multinucleotide-polymorphism | GTG/TTA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255388 | CAATGACAGTGATAT[GTG/TTA]CTACGTATCACAGGA | 286053 |
rs386729618 | multinucleotide-polymorphism | AG/GA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304959 | GAAGGAAGGAAGGAA[AG/GA]AAGAAAGAAAAAGGA | 286053 |
rs386729619 | in-del | CC/TCTTTATTTCCTTCT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316633 | TTTCCTTCTTTCCTT[CC/TCTTTATTTCCTTCT]TTCCTTCTTTCCTTC | 286053 |
rs397687521 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240143 | TCTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 286053 |
rs397694463 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328853 | AATATCCAAGGTCAT[-/T]TAGTCCCAACCCTCT | 286053 |
rs397747400 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235258 | TAAAAAAAAAAAAAA[-/A]GGAAACCTAAAAGCT | 286053 |
rs397765906 | in-del | -/TA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272716 | ATATATATATATATA[-/TA]ATATATATATATACA | 286053 |
rs397773131 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265168 | ATTTAATTTTTTTTT[-/T]GGTAGTTCATGAATT | 286053 |
rs397776783 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183419 | TTTGTTCTTTTTTTT[-/T]AACATCACAGCTCCC | 286053 |
rs397801250 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328854 | ATATCCAAGGTCATT[-/T]AGTCCCAACCCTCTC | 286053 |
rs397818627 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161807 | AAAAAAAAAAAAAAA[-/A]TCGGAAACGGTAACC | 286053 |
rs397892011 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120581 | GTTTCTTACGATATT[-/G]GGCAAGCCAGAGGTT | 286053 |
rs397937442 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297843 | GTCTCAAAAAAAAAA[-/A]TTATTGATTACTTTT | 286053 |
rs397958207 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103840 | AGAATCTTTTTTTTT[-/T]AGTCTTCCATTTCTT | 286053 |
rs397961931 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244041 | AAGAGTTTTTTTTTT[-/T]AAGTAGCATAGAATT | 286053 |
rs398009770 | in-del | -/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113068 | AAAATGGGGGGGGGG[-/G]TGAGTCAATACCTAC | 286053 |
rs398009772 | in-del | -/T | 0 | 0 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125195904 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAT | 286053 |
rs398009773 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216650 | AAAAAAAAAAAAAAA[-/A]TGGTCTATGGGTTTT | 286053 |
rs398009774 | in-del | -/AT | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236379 | ACTATATATATATAT[-/AT]CATATGATCCCATAC | 286053 |
rs398009775 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262934 | TGCCTCCGCGAAAAA[-/A]GGTTGAAGATGAGTA | 286053 |
rs398009777 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296412 | TTTTTTTTTTTTTTT[-/T]GAAACGGAGTCTTGC | 286053 |
rs398009779 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338298 | GAAAAAAAAAAAAAA[-/A]GCTGCCTTTTATATA | 286053 |
rs398009780 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361080 | TCCTTTTTTTTTTTT[-/T]CGTTTCTTTTTTCTT | 286053 |
rs398047399 | in-del | -/A | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239609 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs398068244 | in-del | -/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331598 | ACGATCTTTTTTTTT[-/TT]AACAAAATAACCAGA | 286053 |
rs398086978 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132509 | TTTTGGTTTTTTTTT[-/T]TGAGACAGGATCTCA | 286053 |
rs398086979 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169740 | CATTTGATTTTTTTT[-/T]TCCTGCCTTTTCCAT | 286053 |
rs398086980 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230301 | TTACTGAACTAATAC[-/C]CTATAAAGCCTTACC | 286053 |
rs398086981 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315120 | TAGAATCTTTTTTTT[-/T]TCTTTTTTCTTTTCA | 286053 |
rs527238886 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124199 | AGGTTTTCAAGGTTC[A/C]TCCATGTTGCATGTA | 286053 |
rs527239723 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217158 | ACCACCAAGCTACCC[C/G]TTTGATAGTTGTTCC | 286053 |
rs527239776 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272896 | GTGTATATATATATA[A/T]AAGGCTGTGTAATAC | 286053 |
rs527285522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233057 | CTACAGGGATGTGAC[C/G]TTACGGAAAAGTAAG | 286053 |
rs527286842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175961 | AACAAGCCTCTATAT[A/G]GACAGAGCCATTTGG | 286053 |
rs527288620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168132 | TTTTATTTTTTTTTG[C/T]GGACTACTTATGAGT | 286053 |
rs527303560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124771 | ACATGAGCCACTGCA[C/T]CCAGCCTCCTCAGGA | 286053 |
rs527344738 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290301 | ACTAATACAAGGTAG[C/T]GGTAGCAAAAAAAAA | 286053 |
rs527350997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216588 | GCGGTGATCCGAGAT[C/T]GCACCATTGCACTCC | 286053 |
rs527362190 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163674 | GTCCTCATCTGACAA[-/C]CCCATATCTGAATGG | 286053 |
rs527374088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131566 | CTTGCCCAGCCAACA[A/G]GTGCAACACCATGGT | 286053 |
rs527381411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267160 | ATATAGGCACGCACT[C/G]CCACGCCCGGTTAAT | 286053 |
rs527410561 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347526 | TTTGTATCTATACCT[A/G]GAATTTGGTGTAGTG | 286053 |
rs527413115 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317523 | TTTAATATATACTTC[C/T]TCCCTCCTCCATGCT | 286053 |
rs527419963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313436 | TTCTAAAAATGGCAC[A/G]TGGAAAACACTTTAA | 286053 |
rs527420012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182811 | CAAGTTTTTTAGTGG[A/G]CATAATTTTGACTTA | 286053 |
rs527463418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145718 | CTTTGAGCTCTATTC[A/G]GAAGTAATTCTGCAA | 286053 |
rs527464120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239126 | TTTGGCAAGGTTGGT[C/T]TCATGGACTGAGCCA | 286053 |
rs527472338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335062 | TACCTGACCAGATTG[C/T]GAAGTATCTTGAAGC | 286053 |
rs527480960 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143275 | ATTTTATCCAAAAAG[A/T]ATAGATGTCTTCTTT | 286053 |
rs527486170 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109072 | TGAAAAAGAAAATAA[C/G]TTTGACTAAGGTATT | 286053 |
rs527508079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095216 | TGCAGATTATAGAAC[A/G]TTTTCATCACAGAAA | 286053 |
rs527522445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334453 | AGAGCCTAGAAGGAG[C/G]ATGGGGACACCCATT | 286053 |
rs527527317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246356 | GCCCGACTAATTTTT[C/G]TATTTTTAGTAGAGA | 286053 |
rs527545317 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112112 | AACCCTAAGAAGCCA[A/G]TGTTTGTATGCTTAT | 286053 |
rs527555723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328953 | GCACCTTCTTGGCTG[A/C]CTGCATGAGGCCTGT | 286053 |
rs527559988 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269160 | TGACACGATCTCGAC[A/T]CACTTCAACCTCCTC | 286053 |
rs527563896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279116 | GTTAAATACATATAT[A/G]TTTTTCAAAGGAAAT | 286053 |
rs527575687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201999 | AGTGAGCAAGGCTCC[G/T]TCGGCATGGGACCTG | 286053 |
rs527597437 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204556 | ACAAAGTATTAAGTT[G/T]ACCATACTTCTTATA | 286053 |
rs527597454 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175097 | TGATTCTCAGCTTGG[A/G]CATGCCTTTTAAGAA | 286053 |
rs527625335 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285975 | TGGCCATTAGGATGT[A/T]CCTTGGAATCCCATT | 286053 |
rs527635992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202570 | TAGTAATATAATAAT[A/T]ATGCTAACTAGCCCA | 286053 |
rs527650827 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116609 | ACACATGGGAGTGTC[-/TG]TGTTTTGAAAGGACA | 286053 |
rs527653692 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140396 | GGCCAGGCACAGTGG[C/T]TCACGCCTGTAATCC | 286053 |
rs527668270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241769 | TGAGTTGAAAATATA[A/G]GAATTGGAAATCACA | 286053 |
rs527675118 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256945 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAA]GAGGGCTGAAGGTGA | 286053 |
rs527675868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330105 | TACAGATTCGGGGCA[C/T]GTCGCTTTCAGAAGG | 286053 |
rs527676304 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337724 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 286053 |
rs527687348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191822 | TACAACATCCACACG[C/T]AGGAAAGGAATGCAT | 286053 |
rs527689177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184145 | TCCAATCACAATTCC[C/T]GAGTTTTAAGTAATT | 286053 |
rs527699356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089958 | TTAATGCAAAAGCAT[A/T]TGAGTTATATTTAAT | 286053 |
rs527700773 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205507 | GATGGTGCATCCCAG[C/G]AGACACACTGACTGA | 286053 |
rs527711824 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207726 | GTCTTCTGCCGGTTA[-/G]GAGGGGCTTCCTCAC | 286053 |
rs527728185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248482 | ACATAGTAAAACCCC[A/G]TCTCTACTAAAAATA | 286053 |
rs527743441 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234679 | ACTTTTCTTTCCCAT[C/G]AAACCAGTTATAAAC | 286053 |
rs527761885 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231225 | CAGGTAGCAGTAGGG[G/T]GACCTAATACACAGA | 286053 |
rs527763166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138059 | AAGATTGAAATTCAG[A/G]AAGACTTTCTTTTTA | 286053 |
rs527784962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147403 | ATCCTAAGAACACTA[A/G]GGCATCATTCTTGTC | 286053 |
rs527786343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330616 | GCCAAAAATAAGCTC[A/G]CACCTGGGCAACTCC | 286053 |
rs527800094 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159736 | ATTGCTCAGTTGGTG[A/G]ATCACTTGCGGTCAG | 286053 |
rs527803119 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208667 | AAGTGTTTCATACAA[A/T]TAACACCTGAGAAGG | 286053 |
rs527805461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242346 | ACAGCTGAAGGGCAT[A/G]TTGGATGGGCTCCTG | 286053 |
rs527822078 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287863 | AGTTTTCCAATCCAT[A/G]TCTTCCTAAGTCTCT | 286053 |
rs527822181 | in-del | -/AGTG | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270886 | CAACCAGGGCAACAT[-/AGTG]AGACACCATCTCTTA | 286053 |
rs527822606 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141247 | TGAGGTAGAGCAATT[C/T]ATTTAAGTCAATCAG | 286053 |
rs527840076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202586 | ATGCTAACTAGCCCA[C/T]AGAGTTGTTTATGGG | 286053 |
rs527842585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343962 | AGTGAGCCGAGATCG[C/T]GCCACTGCACACCAG | 286053 |
rs527842691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210616 | CCCTTTTCAGCCTAA[A/T]AATTGCCTCATTTTG | 286053 |
rs527855942 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154121 | ACTTTTGCAAATTGC[C/G]ATACTTCCGTTACTA | 286053 |
rs527857783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162627 | GATTAAAAAAATGAG[A/G]TAACATTATGTGAAA | 286053 |
rs527883405 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141189 | ATACATTCTAAGGAT[A/G]TATCTGTCTATATAA | 286053 |
rs527890946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307105 | CATGGAGGAAAGAGT[A/C]CAGCATTTGTTTCCT | 286053 |
rs527895793 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300008 | ATTTTTAGTAGAGAC[A/G]GGGTTTCAACATGTT | 286053 |
rs527897213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203171 | TCTTTGCTGTTTGAG[C/T]TCAGTTGTTTAGTTA | 286053 |
rs527901848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197141 | ATATTCTCCCATTCT[C/G]TAGGTTGCCTGTTCA | 286053 |
rs527915502 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169473 | TTTTCTCCTGGGATT[C/G]TGTAACTTCGTAAAT | 286053 |
rs527917707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357906 | AGGAAGAGGCACTTC[A/G]ATGTCTCTTCTAAAT | 286053 |
rs527940178 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168670 | GAGGGCTTTGCCCTC[A/G]TGCTCTAATCTCTTC | 286053 |
rs527954014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117511 | TTTCTTTGTTCCATG[A/G]GGCTTTTTGCATTTA | 286053 |
rs527962721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293647 | AAACATTATGAGGTT[C/G]CTGAGACTTTTGAAG | 286053 |
rs527982200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209764 | GTGGTGAATTCTAGA[A/G]AATTCTTTAGGGGAA | 286053 |
rs527994483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247837 | CCATTTTCAGTCATT[A/G]TTACTAAGACAAGTT | 286053 |
rs528006435 | snp | A/G | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367384 | TCCAGGTGTGGTGGT[A/G]CGCACCTGTAATCCT | 286053 |
rs528009450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344532 | GCAATCACCTGAGGT[A/C]AGGAGTTTGAGACCA | 286053 |
rs528021621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300584 | ACAGTCATTTATTGA[A/G]CATCTCTTATTCGCT | 286053 |
rs528030317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111103 | ACTTGTGTTCTGGCT[A/G]AGAATCATCACCTTT | 286053 |
rs528034153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204772 | CCCATTCCTAAAAAT[C/T]CCTACCAGTCCCCTC | 286053 |
rs528045153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256795 | CTGGGCGTGGTGGCA[A/C]ATGCCTGTAGTCCCA | 286053 |
rs528075151 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134124 | TATTCTGGTGAGGGG[A/G]TTATACATTAAAAGC | 286053 |
rs528077557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105532 | TAAAATACAACATGT[C/G]CAATTTAAGAAGAAT | 286053 |
rs528087053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302087 | CCTCAGCCTCCCAGA[A/G]CTGGGATTACAGGTG | 286053 |
rs528095316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098146 | GGTCCCTTCCCAGAC[A/G]TACTGAATTAGAAAT | 286053 |
rs528112889 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094447 | AATTCAATCTCAGTC[A/T]TAATCTTTTCCCTAC | 286053 |
rs528114945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149068 | ACTGTGACTCTAATA[C/G]TCTAACAATTTTACC | 286053 |
rs528116847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353185 | GTTATTCATCCAGCA[A/G]ATTTTCTGGTGAATT | 286053 |
rs528123387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255973 | TGGTTTTAAAAAGAA[A/G]TATTTAGAGGGTAAA | 286053 |
rs528151464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171153 | ACCGTCCATCACAGA[A/G]GAGCTCACTCATTTC | 286053 |
rs528155281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163527 | TTCCTCATTTCTAAA[A/G]TGGGGTAATAATAGT | 286053 |
rs528157067 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101196 | CATGGTAGGTACTCA[A/G]TACTTATGAGTGAAA | 286053 |
rs528165825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212225 | CCTTGTTAGCAAGGC[A/G]AACACATATTCATTT | 286053 |
rs528173563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295864 | TGACTAAAATATTAT[C/T]TTGGATGAAACTGAA | 286053 |
rs528182140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250066 | GCAATCTCGGCTCAC[C/T]GCAACCTCCGTCTCC | 286053 |
rs528187688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338774 | TTATAAATGAAATTT[A/G]TTCTAGGAGTAATAA | 286053 |
rs528207982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191508 | ACTTTGATGACGCTG[A/G]AGGAATCTGCTTCAT | 286053 |
rs528209679 | snp | A/G | 0.008801 | 0.0657499 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156014 | GCTAGGTGTGGTGGC[A/G]CACGCCTGTAGTTCC | 286053 |
rs528224880 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194049 | AAATGTATTGTATGC[A/G]TGACTGTATTTCATA | 286053 |
rs528229768 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112624 | AGATGTTTTGCTAAG[C/T]AAAATAAGCCAGTCA | 286053 |
rs528236044 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286967 | TGGGAGGTGAACTCC[C/T]GATCTCACTGTAACG | 286053 |
rs528244597 | snp | A/C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280723 | TGTTTGGGTCCCAGA[A/C/T]AGGAGAAAGCCTTTA | 286053 |
rs528245256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126327 | AGTGAGCCGAGATTG[C/T]GCCATAGCACTCCAG | 286053 |
rs528253065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358854 | CTTGATGGTCATTCA[A/G]GCAAATAACTTATCC | 286053 |
rs528261910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366494 | GCAGTGAGCCAGGAT[C/T]GTGCCACTGCACTCC | 286053 |
rs528268916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226801 | GGAGGAAGACACTTT[C/G]TTCCCCTTACTCCTC | 286053 |
rs528293186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274885 | CAGTGAGCCAAGATC[A/G]CGCCATTGCACTCCA | 286053 |
rs528334734 | in-del | -/AAGA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313229 | AAAAGAAAGAAAAAG[-/AAGA]AAGAAAGAAAGAAAG | 286053 |
rs528341088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090899 | GAAAAGTTCTGAAAT[G/T]AGGCTGAACCTGAAA | 286053 |
rs528342566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184930 | GATTAGAAAATAGAG[C/G]CCAGAGAGAGAGACT | 286053 |
rs528347061 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199088 | CTCTCTTTTCTTCTT[C/T]ATTAGTCTTGCTAGT | 286053 |
rs528361508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176913 | TTGGCCTGCACTTAT[C/T]GTGAGTTTCCTCATA | 286053 |
rs528365610 | snp | A/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164239 | TTAGGAAAGGTGGCT[A/G/T]TTGTTGACTCTGAGC | 286053 |
rs528367602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352500 | AAAAAAAAAATTTGG[G/T]AGCAGAGGAGCTCCC | 286053 |
rs528388984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262519 | CATCCATTTATTAGT[A/G]TTCATCCATTTATTG | 286053 |
rs528397778 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310432 | TACCTACCATATGAT[A/G]AGTGCCCAATCAATT | 286053 |
rs528404219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315950 | TGTGACCATAGGCAC[A/G]CACCACCACATCCAG | 286053 |
rs528406293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308160 | AACCTTCTCTTAGAA[C/T]GTGGTGCCATGTTCT | 286053 |
rs528408744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218230 | CTGACCAAAATACTA[A/G]CCACCATGTCTACTG | 286053 |
rs528423763 | snp | A/G | | | intron-variant, missense | NSMCE2 | GRCh38.p7 | 8:125130286 | TAGTGCAAGTCATCA[A/G]CATGACCAGTAATGT | 286053 |
rs528431115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121096 | GTGTTTATTACTACT[A/G]TTATAGTAGAGCCAG | 286053 |
rs528434135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361283 | ATGTTGTCCAGGCTG[G/T]TCTCGAACTCCTGGC | 286053 |
rs528455657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271028 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 286053 |
rs528460723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212832 | TTCAGCCCGGGTTCT[A/G]ATCACCGAGGCATGT | 286053 |
rs528476226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360532 | GAGAGGATCAATCAG[C/T]GGAAGAAGACCCCTA | 286053 |
rs528484745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229113 | GGTAGAATGAAGGAT[C/G]ATGAGTCAGAAAAAA | 286053 |
rs528484970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172562 | ATCTTACCAGGTACC[A/G]TTTCCAGCTTGAAGT | 286053 |
rs528491734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305877 | TAGTCTAGTGGAGAG[G/T]CTTAGTAAAAAATCC | 286053 |
rs528499388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121714 | GCCAACTTGTGATGC[G/T]TTTTGTGTACCTGGC | 286053 |
rs528507208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270457 | GTGACAGAGCGAGAC[G/T]GTGTCTCAAAGCAAA | 286053 |
rs528518639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276908 | CTGCATTGCACAACT[A/G]TGGGGGACACCATTC | 286053 |
rs528537867 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302433 | AGTGAGGGAAAGGAA[A/G]GTAGGAGATGAGATC | 286053 |
rs528552375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303583 | TTCTGCACCCCCTCT[C/T]GCTGTTTAGGAAAAG | 286053 |
rs528553677 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332658 | ATATTACAAGTTTTC[G/T]TTTAAACAGAATGCT | 286053 |
rs528556394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354972 | TGAGTGTTAAAAATG[A/C]TGCATAAAATTAGCT | 286053 |
rs528558895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127639 | CGTTCTGGAGTTTGT[G/T]GAGCATTACCCTGTA | 286053 |
rs528560420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178964 | GGAAATTTGGACACA[C/G]ACCTGTGTAGAGGGA | 286053 |
rs528595255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265955 | TTATTTGATTTGTAA[A/G]CATTTCTGGATGAAT | 286053 |
rs528619051 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330766 | CCAGAGGCTTTGGAG[C/G]AGTGATGATCACCCA | 286053 |
rs528633812 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310453 | CCAATCAATTGTAGC[A/T]ATTGCAATTATGTAA | 286053 |
rs528648773 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243902 | AAGATCATCTTTGTC[A/T]CTGAAAGACTCACAA | 286053 |
rs528659362 | in-del | -/T | 0.323197 | 0.239044 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240130 | CAGTTTTTCTTTTTC[-/T]TTTTTTTTTTTTTGA | 286053 |
rs528666147 | in-del | -/GAG | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150993 | GAAGCATCATATGGT[-/GAG]GAGGTTTTTTTTATT | 286053 |
rs528666760 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122045 | CTAGGCCTGTGCTCA[C/G]TGTAGATAGCTCTTT | 286053 |
rs528669667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332145 | AAATTTTATTTATTA[A/T]CCTCTTCCCATTTGA | 286053 |
rs528672293 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223940 | CTTCCTGGTTCAAGA[C/G]ATTCTCCCACTGTAG | 286053 |
rs528672738 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092282 | CTTCAGTTATGTAGA[C/T]TGCAGTGAGAATTAG | 286053 |
rs528688928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339139 | CACTGCTCTGCAGTG[C/T]CTTCTGTCAGGTCTG | 286053 |
rs528714533 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282082 | GTTTTTCTAGAGAAA[C/T]CGGATGTTTGGATTT | 286053 |
rs528728268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250577 | TTGTCTTAAATTTTT[A/G]TAGCTATAATTTCAT | 286053 |
rs528741152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228382 | TTCTAGAAGCTTACA[A/G]TTCAGTGATGGTAAC | 286053 |
rs528753227 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316768 | TTCCTTCCTTCCTTC[C/T]TTCTCTCTCTCTCTT | 286053 |
rs528756785 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254439 | GAAAATTAACCATGC[C/T]CATTCAGATTCTGAA | 286053 |
rs528759803 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192945 | TACTTTAAGGAGATG[G/T]TCTGAAGTAATGAAG | 286053 |
rs528782173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141933 | AATGAGTTTCTGAAC[C/T]TGGGGGAGGGGTATG | 286053 |
rs528782957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236367 | ACGAGTTGCAAAACT[A/G]TATATATATATATCA | 286053 |
rs528785135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149780 | CTGAAATATTTGTGG[A/G]TCTGTTTCTGCTGAT | 286053 |
rs528807411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099405 | ATCATGGCAGAGGGA[A/G]CCAAGAAGGCATAGC | 286053 |
rs528815493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285018 | ATCTGTTTGAATGAT[A/G]CGGCATGAAAAGGAT | 286053 |
rs528815951 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278394 | AATGTAGGAAGTTGG[A/G]GGTGGCACAGAAGCC | 286053 |
rs528822294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193497 | TAAACACTGCTGGTT[C/G]TAGCATTATGCTTCT | 286053 |
rs528834735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185660 | GTTCATTGGTTATAT[C/T]AACTGACATTTATCA | 286053 |
rs528841514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277780 | CGGCCTCCCAGAGTG[C/G]TGGGATTACAGGCGT | 286053 |
rs528844474 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299306 | AGGAGCACTCTATTC[A/G]TTTCTTTTCACACTG | 286053 |
rs528846443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137201 | TCTTTCCTGAAAGAA[A/G]TGTTTCTCCCCACAA | 286053 |
rs528858407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180696 | ATTTGACTTCTTTCT[A/G]AATCATTTTATTTAT | 286053 |
rs528875218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326672 | AAAAGATAAAAAAGG[C/T]GGGCCAGGCGCAATG | 286053 |
rs528883144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188681 | ATGAGAGACGGCAGC[C/T]GTTTAATTTACTGTT | 286053 |
rs528889472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334309 | TACTATCTGTAGCAC[A/T]GCGCTCCAGGCTGTG | 286053 |
rs528926683 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125130097 | TTCTTAGTTGGTTTC[A/G]CTTTTTTTTTTCTTG | 286053 |
rs528927086 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333735 | AGCCGGGATGGTCTC[C/G]ATCTCCTGACCTCGT | 286053 |
rs528940852 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318805 | CCAGCTTACTATTGA[G/T]AGAGTTTTCAGGCCA | 286053 |
rs528943474 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093422 | GCCCTGGCACAGTGG[C/T]TTATGCCTGTAATCC | 286053 |
rs528943589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221957 | TAAAGTAGACACTCA[A/G]TAAAAAAGCTCATTA | 286053 |
rs528950444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278362 | GGTTTGCTTGCCACG[C/G]TGTCTGGTTCCTTCA | 286053 |
rs528961643 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191025 | ACAGGCACCCGCCAC[A/G]CCACCTAGCTAATTT | 286053 |
rs528963503 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194803 | ATTATTTTTCGTTTT[G/T]TTTTTCATTCTGCTA | 286053 |
rs528973111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271723 | ATCAGCGTTCTGGAG[A/G]ATGCATGCTTGATTT | 286053 |
rs528986647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144212 | CAGGGATTCTCTCCA[G/T]TGCATGCCTTAGGCT | 286053 |
rs528998993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318006 | AAATCTTACAAATCA[A/G]TGTGAAAATGACAAA | 286053 |
rs529001598 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171056 | CAAACCCTTTTTACT[C/G]TGACTCCAACTATAT | 286053 |
rs529020383 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238659 | CACCATGAATTTGTT[G/T]GGAATTTACCCACAA | 286053 |
rs529022383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230565 | TTCCTTTTGTCTCTT[G/T]TCTGTTCAGTTTCAA | 286053 |
rs529025180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258580 | CAGATGGAGCATTCT[C/G]TGTGCAACTGGAGGA | 286053 |
rs529030384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158974 | CAGTTATCTGTGGCC[A/G]TCTCTGGTCCAAAAT | 286053 |
rs529030667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150947 | TGCCTTTGAGCTGTC[G/T]TCTACTGAGTGTATT | 286053 |
rs529033862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200552 | AGATCCGCTGTTAGT[C/G]TGATGGGCTTCCCTT | 286053 |
rs529049163 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251606 | CCAAGTTTCCAGCAT[A/G]TATTCCTGGGCAGAA | 286053 |
rs529053963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207026 | TTTTAGTTGAATTTC[C/G]TATTACCAAGGATGC | 286053 |
rs529054102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340776 | TCAGATGAATAGCCC[C/T]CAGTCTGGGTGAAGA | 286053 |
rs529055290 | in-del | -/CTTC | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184465 | ATATTGAAAGAAATA[-/CTTC]CTTATAAAGTTTCCC | 286053 |
rs529068070 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356022 | TAAGGTCAAAACTGT[C/G]TTTATAATAATAGTA | 286053 |
rs529083968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296829 | AGGAAAATGGCCAAG[A/G]TGTACTTTCGTGGAA | 286053 |
rs529103754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200988 | TTGTGCATGCATCAC[A/G]AAGTTCTTGTGCCTT | 286053 |
rs529113436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304054 | CAGAGTTTATTCTCT[A/G]CATAAGATATTAATT | 286053 |
rs529116811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143725 | AATTTCAGGAAACAG[C/T]TTGGCCGTGGGCAAA | 286053 |
rs529123616 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100400 | TATCCTTTAAACTCA[A/G]TTCTATGTTCCCTTC | 286053 |
rs529163997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158399 | AAAGGAGAGAAGGAA[A/G]TGTTTGAGAGGAAAA | 286053 |
rs529168496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290351 | TTAAATAAGCTGTAA[A/G]GAAAAAGGGGTGTCT | 286053 |
rs529186523 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219435 | AGCAAAAATAGCTTA[A/C]GTGTGATTCACTCTG | 286053 |
rs529194522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206369 | CAGGTTTTTCATTAG[C/G]TGAGACATCTGATTA | 286053 |
rs529195553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289878 | GCATTTATTATCAAA[A/G]CCTTTTTGTTTATGA | 286053 |
rs529196133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252117 | GGAGAGTATAGTCAG[C/G]AAAAAGAGGATAGCA | 286053 |
rs529201670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202076 | ACCATGGGAAAAGCA[C/T]AGTATTTTGGCGAGA | 286053 |
rs529212843 | in-del | -/AGAGTA | 0.0755793 | 0.179102 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284263 | ATACCCCTGAAAGAC[-/AGAGTA]TGTCTTCGACTCTCA | 286053 |
rs529220581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341397 | TTTCTCCTTTCTTGC[G/T]TCCTCTGTTTTGTCC | 286053 |
rs529237211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118544 | TCCCATTTGGTAGGA[A/G]ATACCACTAGGTGGC | 286053 |
rs529269971 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102805 | GTATATAAATTTATT[A/T]TGATATTGTTATTTT | 286053 |
rs529284298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253309 | TTTTTTGTGCTCAGC[C/T]CAAAGCCTTGACCAT | 286053 |
rs529292085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153211 | CATCTCATTATCCTC[A/G]AACAGGGAAGATAGA | 286053 |
rs529310803 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147143 | TTCTGTGAATTTGAA[A/C]ATCGTTGTGTGATTT | 286053 |
rs529312969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252763 | TAGAATGAAAGCATA[C/T]CTTTAACTTGTATAA | 286053 |
rs529320713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168010 | AGGTCTCCTTAATCA[C/T]ACAGTTCGGGTATTT | 286053 |
rs529335002 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201823 | TATAGAGGCAGTAGC[C/G/T]CTTGATGAGCTGTGG | 286053 |
rs529335576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350567 | GACTTAACGTTCCAC[A/T]TGGCTGGGGAGGCCT | 286053 |
rs529335895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145993 | CCAATATTAAAACTT[A/G]TTAATCTTCAAAAAG | 286053 |
rs529348596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260205 | ATCTCTGATGAGTCA[C/G]AATAGTGGAAGGGAG | 286053 |
rs529350986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292676 | GTTATCTCTCCAAAA[A/G]CTTCTTACCACCTGT | 286053 |
rs529352950 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210108 | TACTAGCTCTGTAAC[C/G]CGGGATAAGTTTCTA | 286053 |
rs529353959 | in-del | -/ATT | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196600 | TTAATCCAGTCTATC[-/ATT]GTTGGACATTTGGGT | 286053 |
rs529367614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335225 | GAGTGAGGAGGTATG[C/G]GAAGCAGCTCTGGAG | 286053 |
rs529393284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286038 | AGAACAGTCCACTAG[C/T]AGCACTTGTTTCCCT | 286053 |
rs529394277 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241615 | GTTAATAAGAATTGA[A/T]CTGTAACTGAAAAAG | 286053 |
rs529405095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246990 | ATTGTTAACTATAGT[C/G]ACGTTGCTTTACTAT | 286053 |
rs529408442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110179 | TCTCATGCCTCTCTG[C/G]CAGGGCAAGTCTGTG | 286053 |
rs529438867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292094 | GGATTGAGTCACAAG[C/T]ACCACACCTACCTAC | 286053 |
rs529442658 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311936 | AGCCAGGCATGGTGG[C/T]GCATGCCTGTAATCC | 286053 |
rs529442877 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206212 | AGTCACAGGACTTGA[A/G]GAACAGCAAATAAAA | 286053 |
rs529454256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215460 | TGGACATTTGGGTTG[C/G]TTCCAAGTCTTTGCT | 286053 |
rs529463129 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297073 | ACAATCACTTCACTG[A/G]GCCATTTTACTGTGA | 286053 |
rs529471427 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303214 | CTGCAGTTCAGCTTT[A/G]ACTCAGGAGAGCCTG | 286053 |
rs529473444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208048 | TGTGGCCAGATTGTC[A/G]GTCAGCCATCCAGCT | 286053 |
rs529483017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356111 | ACAGGATATGTGATA[C/T]TGTGACAGATTGAAT | 286053 |
rs529487449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222765 | TTAAATCTGTTCATC[A/G]ATGAGAGACTCTTAG | 286053 |
rs529509448 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181310 | TGTGTAAAGGTTCTT[C/G]AGAAAAGAGCCCGTT | 286053 |
rs529515341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305506 | GTCAGGCAGAGATAT[C/T]TTGAAGGCAGCTGGA | 286053 |
rs529521488 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272145 | CAGCCTCCCGAGTAG[C/T]TGGGACTACAGGCGC | 286053 |
rs529529499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123922 | AGGTATGATTCACCC[A/G]TTTAAAATGTACAAT | 286053 |
rs529531642 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298548 | ATTAGCAGGATAATG[C/T]GGGAAATTTACTTAA | 286053 |
rs529532243 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108348 | GAGTAGGAAAACACC[C/G]GTTGTTTAAGGAAAT | 286053 |
rs529561023 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341078 | ACCAGTCACCTCTCC[A/T]TATTTTTTTTTCTTT | 286053 |
rs529563237 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322676 | AGGAGTAGTAAAATT[C/T]GCAGATAACATGATC | 286053 |
rs529566268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266497 | TATTCACCTTCTGGT[C/G]GGGGAAGTGCATCAG | 286053 |
rs529575255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304870 | TTCAGCCTGGGCAAC[A/G]GAGCCAGACTCTGAA | 286053 |
rs529578035 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106211 | CCTTCATAGAGTTTA[C/G]CATCTTAGTGGGAAG | 286053 |
rs529597234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356563 | CGATCTCTTGACCTC[A/G]TGATCCGCCCACCTC | 286053 |
rs529605807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130659 | CTTTCAGCAGACAGA[C/G]CTAGGAAATATGTGT | 286053 |
rs529609064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261024 | ATGAAGCTGACAGAG[A/C]AAAGTATATAATCAT | 286053 |
rs529615937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173956 | TTTGTGTATATAAGG[C/T]TTTGAACCACTCAGA | 286053 |
rs529616668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259365 | GCGAGCATTACCACC[A/T]GAGCTCCACTTTCTG | 286053 |
rs529640806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225808 | TCATTGCTTTTGGCA[A/G]TTGTAGACAAATTAT | 286053 |
rs529646480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169439 | AATTCAGTGTCCCAC[A/G]GTGACGTTTTCCCCA | 286053 |
rs529647303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117660 | AGCTGGGACCAGAGG[C/T]GTGCACCACGATCCC | 286053 |
rs529653165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357531 | GGGACTAAAGTCATG[A/G]CCTACAGGCCAAGTG | 286053 |
rs529655452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210110 | CTAGCTCTGTAACCC[A/G]GGATAAGTTTCTAAA | 286053 |
rs529659111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118218 | GGGCATGGTGGCACA[A/C]GCCTCTAGTCCCAGC | 286053 |
rs529683136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210774 | GCTGGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC | 286053 |
rs529690216 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161866 | GGATTGATTTCCAGA[C/G]ATTCTGACTTGCTTG | 286053 |
rs529692104 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287883 | CCTAAGTCTCTGTGC[A/C]ATTTAAAATTTTTGA | 286053 |
rs529709211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306702 | ATTTATGGACTTTAT[A/C]TTGATATCCAGTCTT | 286053 |
rs529732207 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124834 | GAGTCTTACTCTTTT[A/G]CCCAGCCTGGGGTGC | 286053 |
rs529757768 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315413 | TTTTGAGTCAGACAG[A/G]CCTGCTTTCAAATCA | 286053 |
rs529778236 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351997 | CTAGCCTGGGCAACA[C/G]AGCAAGACTCCATTT | 286053 |
rs529778718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183898 | TTCTCAGTGAAAAGA[C/T]CGAGAACTATTCTAT | 286053 |
rs529778774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176080 | TCTAATTACATGTAG[C/G]TAAGTATTCACAAGT | 286053 |
rs529787525 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217364 | TTATTTATTTATTTT[A/T]TATTTATTTATTTTG | 286053 |
rs529788281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132985 | CTGAGCACCAGTAAG[A/G]TTAAGTTATTAACTC | 286053 |
rs529810629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131614 | TAACGTGGAAAAAAA[A/G]AATGCTTGGAGATTG | 286053 |
rs529815844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139441 | CTGCTAATAAAGACA[C/T]ACCGGAGACTGGTAA | 286053 |
rs529828612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232412 | TAAGCACTGTGCACA[C/T]GATAAGAATTATTGT | 286053 |
rs529832890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329196 | CTCAGTCCCCAGCAG[C/T]GGGCAATCCTTCCTT | 286053 |
rs529833798 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342180 | ATTCTCTGTGGTTCT[A/G]CTTGTGCTCACTCGT | 286053 |
rs529842958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176716 | CATTTATTTACCTCA[C/G]AGCGACACTATACAT | 286053 |
rs529846561 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267299 | GGCCTGAGCCACCGC[A/G]CCCAGCCAAGGGTAC | 286053 |
rs529848549 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238569 | GACTTCATTAAACAG[C/T]ATTTTTTTTCCTTTC | 286053 |
rs529849236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307260 | ATCACATGTGCAATG[C/T]CTATGTTTAGAAATC | 286053 |
rs529855014 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352313 | AGAAACCCCGTCTCT[A/G]CTAAAAATACAAAAT | 286053 |
rs529866969 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221400 | AGTTGTGTACCACCA[C/T]GCCTGGCTAAGTTTT | 286053 |
rs529870599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328517 | CTGGAGTAGATCTGG[A/G]CACCAAGGCCTGCTG | 286053 |
rs529894594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247601 | ATGGTGGCAGGCACC[G/T]GTAATCCCAGCTACT | 286053 |
rs529894827 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089905 | ACCTAGGTAAATCAC[C/T]TTTCTAAAATTCTAT | 286053 |
rs529897014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095363 | AGAGGCCGAGTTGGG[A/G]GGATCACTTGAGCTC | 286053 |
rs529899418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225071 | GTGCCTTCATCCAGT[C/G]GGCTAAATCTGAGAA | 286053 |
rs529904805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321848 | AGTCAGTTTTTGTTG[C/T]TGTTGTTTTTGTTAT | 286053 |
rs529905444 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141027 | GATATGCTTTAAAAT[A/G]ACAGATTCCCATAGC | 286053 |
rs529909377 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264816 | TTCCAACTCTTTATA[A/G]AATAATAATACTGAA | 286053 |
rs529935029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286472 | CGCCCACCACCATGA[C/T]GGCTAATTTTTTGTA | 286053 |
rs529951951 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245333 | GACTTGCCACATTCT[C/G]TCACCATAATGCTGA | 286053 |
rs529981204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189988 | AGCAGGTCTTCATTT[C/T]TTCCTTAAAGATGTT | 286053 |
rs529997865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281950 | TGCTCTGTCTAGCTC[A/G]TAGCTTGCAAACTCT | 286053 |
rs530011245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138702 | TAAGGCAGGTCAACT[C/T]GGTCAAAGGAATTTG | 286053 |
rs530013751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134151 | AAGCTGGTTTCTTTC[A/G]TATTTGTTATGTAAA | 286053 |
rs530018644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146676 | CCGCATGTTCTCACT[C/T]ATAGGTGGGAATTGA | 286053 |
rs530020053 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254990 | TGCCTGCCAATAGAA[-/T]ATGGCAGAAATGACG | 286053 |
rs530042742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177711 | TCTTACTTAAGCTCA[C/T]TTGCATCATTTTCCC | 286053 |
rs530058445 | snp | G/T | 1.66454e-05 | 0.00288486 | missense | NSMCE2 | GRCh38.p7 | 8:125182148 | GATTTAAAATTATTG[G/T]TAGAGAAGAAATTTT | 286053 |
rs530095274 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169402 | TGACATTCTCTACTT[-/A]AAATGTGCTATAGGC | 286053 |
rs530108198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234740 | GCTGTGGCTTTGTTA[C/T]GCCCTTTCAATCATC | 286053 |
rs530113472 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191893 | TAATAAGAATCTTGG[A/C]GGTGACATATTTACC | 286053 |
rs530117653 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201951 | CTTCCTGCGAAGCTT[C/T]AGCCTCGCAGGTTCT | 286053 |
rs530124279 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199711 | TTGGTGCAGAGCTGA[A/G]TTCAAGTCCTGGATA | 286053 |
rs530124430 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259685 | GTTATTGCAGTACCC[A/G]CAAATTTAACAGTAG | 286053 |
rs530132060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288544 | ATCTGGCCTCTCTCT[A/G]TGTCCTGGTCCTTTT | 286053 |
rs530142663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134517 | ATTTTTCTAATGATC[A/G]TTAAAATTGAGTACC | 286053 |
rs530146264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140970 | TGAAAGACACCTGGC[C/T]GTGAAGATTTGGAGG | 286053 |
rs530149194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330674 | TATTTCTTAAGCCTC[A/G]AATGTACGCTAGGTA | 286053 |
rs530151190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126418 | CTTTGCTCACAAGAT[A/G]TGAGGAGATGTGTGA | 286053 |
rs530154353 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323823 | TCATCAAAATTAGGA[A/G]CTTCTGTTCTTCAAG | 286053 |
rs530168659 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312902 | GAGCTGAACCAGCAC[A/G]GGGAGAGCACAGAGA | 286053 |
rs530176704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097913 | AATTTTATTATATAG[A/G]CAGGAGGGAGTTAGG | 286053 |
rs530181019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227467 | AATAACGAATCAAAT[A/G]TTTCTTTCCTTTACT | 286053 |
rs530189393 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257246 | CTGAGATTGTGTCAC[C/T]GCACTCCAACCTAGG | 286053 |
rs530190488 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190634 | ATTTTGTAGTGAGAA[A/G]TTAACTTTTTCTACA | 286053 |
rs530219020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155663 | CTATTAAATAAACCC[A/C]GTGGTAGTACTGTGT | 286053 |
rs530230556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315319 | AGCCCCAGCTTCCAC[A/G]TCAGCAAAGTGGGAA | 286053 |
rs530245590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235442 | AGTGAAAAGATAACT[C/T]CTCTGACCCCAATCC | 286053 |
rs530251310 | in-del | -/ATT | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243642 | ACATATTCTAACAAA[-/ATT]ATTATATTTTAAGGA | 286053 |
rs530261972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091026 | GAGGGAGCTCCATGC[G/T]CTTGCAATCAGGAGA | 286053 |
rs530273484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262363 | TGGGAGGCAGAGCTT[G/T]CAGTGAGCAGAGATC | 286053 |
rs530273519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255152 | ACTTGTCAGCTGTAT[A/G]AATGAGCCATCTTGG | 286053 |
rs530316599 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287961 | CTCAACTAACTCCTG[C/T]ATCTACACCTAAATA | 286053 |
rs530336451 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104849 | CCAGGCCAACCTGAC[A/G]AAACCCTGTCTCTAC | 286053 |
rs530337710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097060 | TATATTGTGTAAAAT[A/G]TCTCAACTTGTTTGG | 286053 |
rs530344255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249054 | CACATGCCTTTAATC[C/T]CAGCTACTAGGGAAG | 286053 |
rs530348919 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155009 | CAAATAAATCTTTGA[A/G]TAAATATTTACTGAA | 286053 |
rs530406040 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203334 | ATCATACCCATGGAC[C/G]TTGCATAACTAATAT | 286053 |
rs530410675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211226 | GCACATAGTACAAAC[C/T]TCACAAAGTGCAAAA | 286053 |
rs530411760 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358807 | TCATCTGGGTGTGGA[C/G]TTAGAGATAATATAT | 286053 |
rs530418825 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095408 | AGCTTGGGCAACACA[-/G]GGAGATGGTCGTCTC | 286053 |
rs530435491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337819 | AGAATTGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 286053 |
rs530436332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241857 | GCATTCTGTTAGATA[C/T]GGTGGGGAACAAGAG | 286053 |
rs530436452 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163191 | GGGCAACACGGAAAA[A/C]CCCTGACTCTACAAA | 286053 |
rs530439870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200300 | TTGGCATGTTTTTGC[A/G]GTGGCTGGTACCAGT | 286053 |
rs530443981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099568 | ACAAGGTAGGCAGGT[A/G]CAGAAAGTGCATCAG | 286053 |
rs530458509 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304472 | GGCAAGGAAACGAGA[C/T]AGCAAGTAGTTACAA | 286053 |
rs530475239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236522 | TATGTTGGGAATGGA[A/C]ATGTTTGCATATGTG | 286053 |
rs530484524 | snp | C/T | | | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125099500 | CCTGGGACCCTACAA[C/T]ATATGGAGCTCAAGG | 286053 |
rs530503768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105667 | GTTTCTGTCACAACC[C/T]GCTGTTGTAGTGCAA | 286053 |
rs530510861 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205516 | TCCCAGGAGACACAC[C/T]GACTGAAACACATTA | 286053 |
rs530528805 | in-del | -/TTA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126916 | ACAGCGTTCTTATTT[-/TTA]TATCTGTCAGTTATT | 286053 |
rs530533044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243950 | TAAATCCCCCAAAAA[A/G]CAAAATTTATAAAGA | 286053 |
rs530542063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332236 | AAAATTTGAGAATTC[C/T]ATAAAGGGCATATTT | 286053 |
rs530543844 | in-del | -/TATTC | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201049 | CTTCTCTATACTGTT[-/TATTC]TAGTTAGTCATTCGT | 286053 |
rs530562805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257487 | GAGGAAGGGTCATTG[A/G]TAACTTTTGCCAAGC | 286053 |
rs530563817 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220636 | TGGTGAGTTAACATC[A/G]TTATTTAAAAAAAAA | 286053 |
rs530566344 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296530 | CTCCCTAGTAGCTGG[G/T]ATTACAGGCATGCAC | 286053 |
rs530568945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142671 | GGACAGTGGTGCTAT[C/T]TTGGCTCACCACAAC | 286053 |
rs530581350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164781 | TTTCTAGTTTTAATG[A/G]TATGGTTTATGTTTA | 286053 |
rs530587907 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251646 | AATAGCAAAAATAGC[A/G]ACCACTTATTGGATG | 286053 |
rs530593133 | snp | A/G | | | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125130023 | ATCCTTTTAAAGAAC[A/G]TTGTCTGGGATCCAA | 286053 |
rs530608574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113606 | AAAATGTTCACAATG[A/G]TGTGGATTAGAACCT | 286053 |
rs530609113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171858 | TGATGGAAACGTTCT[A/G]TATCTGCTCTGTCCA | 286053 |
rs530610492 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223748 | GAGCATTTTTTCCAT[A/G]TATTTCTTGGCCACT | 286053 |
rs530611156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309017 | TGGGAGGCCGAGGCG[G/T]GTGGATCACCTGAGG | 286053 |
rs530637794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112669 | GTGCTTGATCTCACT[C/T]GTATGTGGAATCTAA | 286053 |
rs530645783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269685 | TAGTTCATGGAATCT[A/G]ATTAAACCTATAAGC | 286053 |
rs530651086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340529 | TTATTCTCTTTACTT[A/G]TTCCTGCTTTGCCAT | 286053 |
rs530663753 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097841 | AGAATCTCTGATTTG[-/A]AAAAGCGTGTTTGCA | 286053 |
rs530676124 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361670 | GGCAGAAGAGTAGCA[A/G]AAGCACTTAGTTGAA | 286053 |
rs530677480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104266 | AAATCTTGGAATTAC[A/G]GGCATGAGCCTCCAT | 286053 |
rs530681846 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120088 | ATCAATATGAAAGTT[A/C]CTAATATTATTTTGA | 286053 |
rs530684657 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178332 | AGAGCACTCACTGAA[A/T]ACTGGATGAGTAAGC | 286053 |
rs530688032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302797 | TAGACATGTGTTTGC[C/T]ATCACATTGCTGTAG | 286053 |
rs530699121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353410 | CCTGTCCAACTTTCC[C/T]GAGCCATGATGAAGA | 286053 |
rs530727014 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316665 | CCTTCTTTCCTTCCT[C/T]CCTTCTTTCCTTCCT | 286053 |
rs530727043 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309949 | GAAATGTTAAAGCTC[G/T]GCTGTGAGAAACTCA | 286053 |
rs530732100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359796 | CATCTTCAAACTTGA[A/G]CCACTATCAACATCC | 286053 |
rs530737414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361376 | CCTGACCACAGTCAC[G/T]TTTTTGCTTTTTTGT | 286053 |
rs530742476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120940 | TGAATTTACCCTTCC[C/G]TCTTCATTCTACTGC | 286053 |
rs530743210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302154 | TAGAAATGGGGTTTT[A/G]CCATGTTGGCCAGGC | 286053 |
rs530758061 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196205 | AACTTTTTTTTTTCT[C/T]TTTTTTTTTTTTTAT | 286053 |
rs530758854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212581 | CAGTACCAAACCGTT[A/G]GAAGTCATTGCCAGA | 286053 |
rs530774379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122385 | CCGAAAAATGGTAGT[C/T]ATTACCTTCTACAAC | 286053 |
rs530787854 | in-del | -/TAT | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214748 | CCAATATTGATACAC[-/TAT]TATTGAGTTAAGCCC | 286053 |
rs530806514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299606 | GACTACAATTTGAGA[C/T]GAGATTTGGGTGGGG | 286053 |
rs530815445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221538 | CATGAGCCACTGTGC[C/T]CAGCCAGATGTGTCT | 286053 |
rs530820580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346683 | GAGGTATTAAATGCA[C/G]GTGCTCAGTTTGGGA | 286053 |
rs530821309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355039 | TGAAATTCATGTTTA[A/G]TCTTGGGTCCCATCC | 286053 |
rs530827620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256902 | CACTCCAGCCTGGGC[A/G]ACAAAGCAAGACTCT | 286053 |
rs530832843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115426 | CATGTACATTGATTT[A/G]TGTCTTGGAAATATG | 286053 |
rs530870967 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287743 | TCTGACTACCCAGGG[A/G]CCACTTGTTTACTTC | 286053 |
rs530871320 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159786 | CCAACATGGTAAAAC[C/T]CCGTCTCTACTAAAA | 286053 |
rs530872524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219582 | AATTCGCTTGTGCAA[C/T]GATATTAAATAGAGT | 286053 |
rs530905002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125129959 | TCTGGTACATTCCTG[C/T]TGACTAAACTAAATA | 286053 |
rs530925918 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270825 | CAGGTCAAAACTTCC[A/G]TGCTGATGAGTAATG | 286053 |
rs530926206 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166385 | GATTCTTGCGCCTCA[C/G]CCTCCCAAGTAGCTG | 286053 |
rs530938995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165917 | ATAGAGAAAGCAGTG[C/T]CAGAGAATTTGATAG | 286053 |
rs530962719 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281692 | CAATCTTACCCGCCT[C/T]AGCCTCCCAAAGTGC | 286053 |
rs530988723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325956 | AAACTCCGTCTCAAA[A/G]TAAATAAATAAATAA | 286053 |
rs530995221 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172685 | TAGGAGAAAAAGAGA[A/G]GGGGAAATTGGTTAA | 286053 |
rs531016884 | in-del | -/ATG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250970 | AACAACATGCACAAT[-/ATG]ATCCTATTTTTATAA | 286053 |
rs531033945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258672 | TAGAAGGGACTCAAG[A/G]ATGAGAAAAGCCACA | 286053 |
rs531043316 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332975 | TAATCAGTTTTGGAA[C/G]TTGGAAGAGACAGAG | 286053 |
rs531050780 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353689 | GGAGTTCGAGACCAG[C/T]GTGGCCAACATGGCG | 286053 |
rs531054798 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173148 | TCCCTTTTTGTCCCT[C/G]TTCTGTGTCATGAGG | 286053 |
rs531056585 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304186 | TTAATGATTAGCCTC[A/G]TTCGACTCTAATCTA | 286053 |
rs531067807 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092490 | AGTTTAAAGAAGCTG[C/T]AGACATGTGAGCAAA | 286053 |
rs531074299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221066 | GCATTCCCCATATCA[C/T]GGTCATACCCACCCT | 286053 |
rs531081576 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118699 | ATAAAAAGTAAAAAT[A/G]TGTTGATTCTATTAG | 286053 |
rs531100170 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271071 | TCAAGACCAGCCTGA[A/G]CAACATAGTGAGACC | 286053 |
rs531108228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361367 | TATTTCTAACCTGAC[C/G]ACAGTCACTTTTTTG | 286053 |
rs531121492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237327 | TTGACATCTTAAACA[C/T]ACTCACACAGTCTCC | 286053 |
rs531122312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135581 | AATAAGGTACGAGGT[A/G]TAGATCAAAGTTCAG | 286053 |
rs531131825 | snp | C/T | 0.000819336 | 0.0202237 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179793 | CATCCTCACTGCCCC[C/T]ACTCAGTCTTCACCT | 286053 |
rs531140187 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121359 | TTTTGTCCCTTTATT[G/T]TACAATACTGATTCA | 286053 |
rs531154088 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093151 | ATTTCTCACAGTTCC[A/G]GGGCCTGTTTCCTGG | 286053 |
rs531170174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279036 | AGCTATAACCACCAC[A/G]AGGGGAAGTTTTTTA | 286053 |
rs531182040 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138527 | CACTGTGCCTGGCTG[G/T]TTTTTTTGTTGTTTT | 286053 |
rs531196748 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239694 | ATTTAAAAAGAAAAA[G/T]CATACCACTTCCTTC | 286053 |
rs531203108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174005 | TGCAAAGTGTTGTTA[A/G]CAACAATACTGATAA | 286053 |
rs531212501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182019 | TTTTGCTTTGAATTA[A/T]CTGAGATAAAAACAA | 286053 |
rs531230652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285934 | GGATTTGAATTCAGG[A/T]TTGACCTGACCAAAA | 286053 |
rs531238857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131514 | GAATTGAGTTACATC[A/G]TTACATCAGGATATA | 286053 |
rs531242461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334941 | TTTATTTTTTTGTAG[A/T]GGCGGAGTCTCACTA | 286053 |
rs531268862 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302149 | TTTAGTAGAAATGGG[A/G]TTTTGCCATGTTGGC | 286053 |
rs531305859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272632 | ATAACCTTAACACTT[C/T]ATACTGCCACAATAA | 286053 |
rs531312354 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300984 | TCCTGTCTGACTCAC[C/T]GACGTTCCATCCTAT | 286053 |
rs531326975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173680 | GGCAGTTTCATATTC[A/G]GAATATGTGTCTTTT | 286053 |
rs531329274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328256 | ATGTATGAATCTTCA[C/T]GATGCCTCTGTCTTT | 286053 |
rs531348720 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187683 | CAGCAAAGGCAGAAA[C/T]TGAGGGCAGTTGTCA | 286053 |
rs531365570 | snp | A/T | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125195918 | TTGAGATGGAGTCTC[A/T]TTCTGTCACCCAGGC | 286053 |
rs531377717 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252481 | CAGTGAGCTGAGATC[C/G]CGCCACTGCACTCCA | 286053 |
rs531383850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144221 | TCTCCAGTGCATGCC[G/T]TAGGCTACAGCTATA | 286053 |
rs531402493 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268113 | GATGGTGCCACCTGT[A/G]GTTTCAGCTACTCCA | 286053 |
rs531409579 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290433 | TTCTCAGACCATAAA[A/T]TCTCTCATCTCTACT | 286053 |
rs531442143 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300170 | CAAGGGCTGTGCCTC[-/T]TTTTTTTTTTTTATT | 286053 |
rs531463756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222860 | TTGAGCTCCGGAGTT[A/C]AAGACCAGCCTAGGC | 286053 |
rs531469364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181374 | GTAATAAAGAACAGG[A/G]TTGAGAATGGATAGC | 286053 |
rs531487011 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214116 | TATCCCAATATCATT[C/T]CCCTAAGTACTCTTC | 286053 |
rs531493129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207864 | ACATGGTAGCAGTGG[A/G]TAGGCAAGAGCCTCT | 286053 |
rs531519774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246245 | CTGGAGTGCAATGTC[A/G]CAATCTCGGCTCACT | 286053 |
rs531523027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151581 | ATCCTAAAAATTGCA[C/T]GCACCTTGTTTTTAT | 286053 |
rs531524498 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165325 | ATGCACAAGGTAGTT[C/G]TGAAATTAAATTGGA | 286053 |
rs531538097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298271 | TCAAAAAATAAATAA[A/G]TAAAATAGTGCTGAC | 286053 |
rs531545208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195544 | AATATAAATGAACTT[C/T]ATTTACCCATATCTC | 286053 |
rs531550949 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216943 | TACACAGTTAGCGTA[C/G]AGGTAACAAACAGAG | 286053 |
rs531588875 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239018 | TATTTAGATGCTGAT[G/T]AACTAGTCAATGACT | 286053 |
rs531591934 | in-del | -/CA | 0.109149 | 0.206545 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118405 | ACAAACACACACACA[-/CA]CAGAGATTGCTGGAC | 286053 |
rs531592784 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159082 | TGTGCCTTGCTGCTC[A/T]GTCCTGTCTTCATCA | 286053 |
rs531597920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292918 | TTCAAATGTTGGCAG[A/G]TCATACTTGTTGAAG | 286053 |
rs531604125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190298 | GTAAATTTTGACTTA[C/T]ATCATTGCAGCTGAA | 286053 |
rs531611045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285100 | AGTATCAGTTGAACT[A/G]GATCTGAAGGAGCTT | 286053 |
rs531615377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107976 | GTGGCAGAGGTTGCA[A/G]TGAGCTGAGATCACA | 286053 |
rs531641201 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216146 | TATGTTGTAGCATGT[A/G]TTACTATTTCATTCT | 286053 |
rs531656474 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284197 | TAAACATTTAGAGAG[-/T]AAAAAAAAAAAAGAA | 286053 |
rs531657471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334359 | AATGGTCTCTGCCCT[C/T]GAGAACAGCGCTGAG | 286053 |
rs531663179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101268 | ACTACAATAGTAGTT[A/C]AGCTGTGAGATGAAG | 286053 |
rs531667784 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241498 | TCTGGGTCGTTTGTT[A/T]TCTGAAGAAGAAGGA | 286053 |
rs531672384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291010 | TTGGATGAACAGAAA[C/G]TAAGGTAAGCTCTGC | 286053 |
rs531686055 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201646 | TTAGGCTACACAGCG[C/T]TCAGGGACCCACTTG | 286053 |
rs531686207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194938 | ATATCTTCTACATTT[A/G]TTCTTTAATTCATTC | 286053 |
rs531693363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336144 | GATAGGAAGGACAGA[G/T]CATTGAGGCAGAATG | 286053 |
rs531699900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202470 | AATCTGAAATGAGAA[A/T]ATGTAAGTTCAGATA | 286053 |
rs531715241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247749 | AAAAAAGATTTGTTT[C/G]ACTAATGTAGCATTT | 286053 |
rs531730830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293600 | GTTTAGTCATCAAGC[A/G]TACTGATGAGTAGAG | 286053 |
rs531734372 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336947 | TTCTCCTCCAGCTAA[C/G]ACTGTGATTTGGTCA | 286053 |
rs531738974 | in-del | -/TGTGTGTGTGTGTGTGTG | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183646 | GTGGTGTGTGTGTGT[-/TGTGTGTGTGTGTGTGTG]GTGTGTGTGTGTGTG | 286053 |
rs531742406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103506 | TATGGATCTGTCAGC[C/T]TATAGTTTTTTGAAT | 286053 |
rs531744181 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141383 | ATTGATTTCTGTGTA[A/G]TAGTCCAGACACTGG | 286053 |
rs531746064 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177913 | AAAGTCTTACAGTTT[C/T]AGTGATTTGTGCTGC | 286053 |
rs531775338 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267134 | CTCAGCCTCCCAAGT[A/G]ACTGGATTATATATA | 286053 |
rs531777884 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343878 | GGACGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 286053 |
rs531778960 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254181 | AATAATTCAAACTCT[A/G]ATATCTCTATTGAAA | 286053 |
rs531783007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147205 | TTTTCCTATAGAAAA[A/G]TCACACTGAAAATAT | 286053 |
rs531784030 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233131 | TGCATGTTATCATGT[A/G]ATAGTGCTAAAACTT | 286053 |
rs531784889 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139447 | ATAAAGACATACCGG[A/C]GACTGGTAATTTATA | 286053 |
rs531788095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153325 | GGTCTCTGTTCTTTT[A/G]TAGGAAGAAAAAACA | 286053 |
rs531788232 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344611 | AGCCAGGAGTGGTGG[C/T]ATGCACCTGTAATCC | 286053 |
rs531802906 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313275 | AAGAAAAAAGAAAGG[A/G]TGAGAAGGCAGGTAT | 286053 |
rs531819612 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121597 | TGTCTCAATCAAGAA[C/T]CTGTGAATGTATTTT | 286053 |
rs531821279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364345 | TCCACAGATCAGGGC[C/T]AAGAAATACTTTCTT | 286053 |
rs531823501 | snp | A/G/T | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367510 | ACAGAGCAAGCCTCT[A/G/T]AAAAAAAAAAAAAAA | 286053 |
rs531856067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248333 | TGCAAGCATTCAGCA[A/G]AGCATAACATGGTTG | 286053 |
rs531873937 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235068 | CTGGCCAACATGGTG[-/A]AAACCCACCTCTACT | 286053 |
rs531891911 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192100 | TTGTGACTTATTTTA[-/AG]AGAGTATGATGCCAT | 286053 |
rs531893913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208930 | GAAGATTGCTGTCAA[C/T]GTTTTTTTCCTCTCC | 286053 |
rs531900221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116809 | AACAAAGCATAGTGC[C/G]TAATTATCACTATAT | 286053 |
rs531902689 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109757 | AACTTTCTAGCTTAT[G/T]TGAAATGATCACCTT | 286053 |
rs531904044 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340302 | GTGAAAATGCTACTC[A/G]ACTGTCATTGTGAAA | 286053 |
rs531904204 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139570 | GCATGGTGTCAGGTA[A/G]GAGAACCTGTGCAGG | 286053 |
rs531912260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299258 | TGAATCAAGAGGAGA[C/T]TCTTTGTCAGTGTGC | 286053 |
rs531913223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350723 | TGACTATCACAAGAA[C/T]AGCATGGGAAAGATC | 286053 |
rs531913402 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260742 | TGATTCTCATGCCTT[A/G]GCCTCCCGAGTAGCT | 286053 |
rs531934621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352408 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 286053 |
rs531950491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356706 | TAAATATAACCCACA[A/T]AGAAAAAGCTTAAAA | 286053 |
rs531954173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110393 | CAGTTACTATGGTCA[A/G]GCAGTTAATTGGGTA | 286053 |
rs531958141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266670 | ATAAGGTTCAGGCTT[G/T]CATGAGAATTTCAGA | 286053 |
rs531962910 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117436 | AAGTGTTCCTCCTTC[C/T]TAAGATACCATAATT | 286053 |
rs531986087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262490 | ACTTTCCTTTAGTTT[A/G]CCATTCATTCATTCA | 286053 |
rs532001912 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341482 | GCTTTGAAAATGCGA[A/T]GCAAGATCAACCAGT | 286053 |
rs532029442 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351229 | ACATCTTGGGGTCCA[A/G]TCAATGCCCTCATGA | 286053 |
rs532055569 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345199 | CTAAATACGTATGTG[A/G]AGTAGTTTATTTCTT | 286053 |
rs532062803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353057 | TCCCCACTCAGCCTT[C/G]CCTAGTGGTAGGCAT | 286053 |
rs532066379 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186962 | ATAACATCTTTGAAC[A/G]AAGAATTTTATCCTT | 286053 |
rs532075261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118312 | GAACCTGCCAGGAGG[A/C]AGAGGTTGCAGTGAG | 286053 |
rs532084141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216529 | CTGTAATCCCAGCTA[C/T]GTACTGAGGCAGGAG | 286053 |
rs532118839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255810 | AAATCCTTCTATCAG[C/G]AGTGGGGAAGGTGGA | 286053 |
rs532152337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322154 | GGAGAGTCGCTTGAG[C/G]CCAGGAGTTTGAGAC | 286053 |
rs532170483 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249333 | CACTTAATCTGCTTC[A/G]AGAGTAAGTTTGGAT | 286053 |
rs532181857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268621 | AAAATGAAATATTTA[C/G]AAATTGCATATCCAA | 286053 |
rs532182382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133126 | ATTAATTAGATTTTT[A/T]AAATCCATTTTAAAT | 286053 |
rs532191539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177405 | AGTATCTTTAGCACT[C/T]TCATTCCCATGATCT | 286053 |
rs532200402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233899 | GAAAAATCTCTGACC[A/G]GGCATGGTGGCTCAT | 286053 |
rs532229484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210828 | GGGGTTCAAGCGATT[C/G]TTATGCCTCAGCCTC | 286053 |
rs532233391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126261 | TGGTGGTGGGTGCCT[A/G]CTAAGGAGGCCGAGG | 286053 |
rs532247212 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171293 | TTCTCTTGACTGCTG[C/T]GTTCCCAGCTCCTGG | 286053 |
rs532252086 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181136 | AGCAAAGTGATAAGG[C/T]AGCAGCTTGACTATA | 286053 |
rs532258883 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315032 | AATTAGGCACAAAGA[A/C]TCACATAAGGCGAAA | 286053 |
rs532270830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301469 | CTCACTACATGGAGG[C/T]GGCGGTGGGGTGGTG | 286053 |
rs532313801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089923 | TCTAAAATTCTATAT[A/C]TAAACTTTATATTAA | 286053 |
rs532367629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261072 | CGATATTTACATTTC[A/G]GTGAAAAGGGGGAGA | 286053 |
rs532386044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307400 | CATAATGTGTTGTCA[A/G]ATCAGAAAGGGAATG | 286053 |
rs532386673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275825 | AAGTGACATAATGAG[C/T]TAGTAATTGTAAGAG | 286053 |
rs532406070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183173 | TACCTCGTGTCCTTA[C/T]ATGTGCTTAATGTAG | 286053 |
rs532414667 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358136 | TCAGGAGTTCAAGAC[C/T]AGCCTGGCCAACATG | 286053 |
rs532436403 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274825 | ATCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 286053 |
rs532436771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120214 | GTATTAGATAACAGC[A/C]CAGATATAGGTTATT | 286053 |
rs532454592 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309810 | CAAAAAGTTTTTAGT[A/G]GCTTCAGTAGGTCTG | 286053 |
rs532455477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140225 | ATGATTCAGTAGATA[C/G]TAGCTTAAGTGAAGA | 286053 |
rs532468270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270412 | GGAGGTTGCAGTGAG[C/T]CGAGATCGCACCACT | 286053 |
rs532468801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185585 | TGTTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 286053 |
rs532480735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360391 | GCATTCACCAGCAGA[A/G]AGCCAGCAAGGCAGG | 286053 |
rs532517920 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199546 | TGTGGTCTGAGAGTT[G/T]GTTGTGATTTCTCTT | 286053 |
rs532521570 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309620 | GTCCCAGCTACTTAG[A/G]AGGCTGAGGCAGGAG | 286053 |
rs532524591 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336180 | GCAAACACCTCTAGT[A/G]TCATGGAATCCAGGG | 286053 |
rs532526341 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324871 | GAGCCACCGCGCCCG[G/T]CCCATTTTGATAAAA | 286053 |
rs532529830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236263 | GTGGTAGCTGTACGG[A/G]ATAATTATTTTCTAA | 286053 |
rs532530402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178422 | GTAAGTATGGTACCT[A/C]CTATTTACTTCTCAG | 286053 |
rs532543975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366617 | CTGGCTCAGGTAGGG[A/T]CTCAGTGAATAAATG | 286053 |
rs532545291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249775 | GCAAAAATGTTTTTT[C/T]CCCAAAACCTGACAT | 286053 |
rs532550963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242710 | AAGAGGAGGGGGGAC[A/G]TATTTTGAAATGTCT | 286053 |
rs532556063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281805 | GGCTGTTGTCAAACT[C/T]CTGGCCTCAAGCAAT | 286053 |
rs532573964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127563 | GTTACATGGAAGATG[C/G]AGTTTTTGTTAGTTG | 286053 |
rs532588698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323952 | ATCTCTCAAAACTCA[A/G]TAAGAAGAAAGCACT | 286053 |
rs532595212 | snp | C/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129011 | CACAGCAGATAAGAA[C/G]ACGTTTTACAGAGGA | 286053 |
rs532605252 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091732 | TCCGCAGTCCCGGAC[C/T]TGGAGCGGGTCAGAC | 286053 |
rs532612981 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229346 | CTTTTTTTTAAATCA[-/C]ACATCCTTAATAGTA | 286053 |
rs532613571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141835 | TTTCTATAGGCAGTG[G/T]TAGCTGCCCGTTCTT | 286053 |
rs532615520 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249160 | TGGGTGACGGAGCAA[A/G]ACTCTGTCTCAAAAA | 286053 |
rs532615752 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346468 | GGGCGCTCCTTACCT[G/T]CTGATCTTTGCTTTC | 286053 |
rs532618490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219848 | ACTGTCAATATCAAG[C/T]AGGATTCATTAATTT | 286053 |
rs532665825 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316726 | TTTCCTTCTTTCTTT[A/C]CTTCTTTTCCTTCCT | 286053 |
rs532671382 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186315 | TTAGCAAAACTTACC[A/C/G]TATTTATTATCTGAC | 286053 |
rs532674524 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128051 | GCTCACCTTTATTAG[A/G]AATACAGCATTGACT | 286053 |
rs532687343 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222044 | TCTTTTTATTTATAT[A/G]TATACTCATTTGTCA | 286053 |
rs532699539 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148320 | TTGAACCAGCTTACT[A/G]TCTGGCTCAGGTCTT | 286053 |
rs532721922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098070 | AGTGGTCTTCAAAGT[G/T]TAATTCTTGGATCAG | 286053 |
rs532732470 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288638 | GTTGTTACTGTTGAC[A/G]TTTATTCATTCTTAT | 286053 |
rs532738371 | snp | A/G | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093456 | CACTTTGGGAGGCCA[A/G]GGCGGGCGGATCACT | 286053 |
rs532757313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098776 | AAGATGGGGCAGGTT[G/T]TAAAAGGAGTAGGTT | 286053 |
rs532765065 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192791 | CAGTTTCTGTCTCTG[C/G]ATCTCATGTCCTCAC | 286053 |
rs532767136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091213 | GCGAGCAGCAATGAC[C/T]TGCCCAAACTCACAG | 286053 |
rs532772143 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194717 | TTATTTATAAAATTT[A/T]AAAAAAAAGAAATGG | 286053 |
rs532817608 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347002 | TTCAGAGGAGTGTGT[C/T]GAAAGAGCCATGGAA | 286053 |
rs532826812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204675 | ACATTTACCAAAAGC[A/C]GAAAATTCCTACTGC | 286053 |
rs532837378 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198458 | AAGCATGTGGTTTTT[C/G]TCATTGGTTCTGTTT | 286053 |
rs532859524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156639 | TGATATGCTAACCTG[A/G]ACATTTTATATGCCT | 286053 |
rs532866261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277123 | AAGTGCTTTCTTCAT[C/T]TTTGTGTCCTCTGCC | 286053 |
rs532870017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105349 | TAGGCCTGGATAAAA[A/G]TCATAATAAAATCTT | 286053 |
rs532899562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192055 | GCAGCAAGTTTAAAC[A/G]CAAACTGTGAACTCT | 286053 |
rs532905352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198957 | CCATTTCTTCTAGAT[C/T]TTCTAGTTTATTTGT | 286053 |
rs532906649 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237406 | ATTAATGTCACTGTT[A/T]CGGTTCCTAACAAAG | 286053 |
rs532943348 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165837 | AGGAGAATTAGAAGG[C/G]AAAAGGCAATTTGAT | 286053 |
rs532946083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341329 | ATTTGGGATCTTTAT[A/G]TTTTCCTGTAGAGTT | 286053 |
rs532957454 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220223 | AGAATCTAAAACTAT[A/G]TATATGAGGATGGTT | 286053 |
rs532958445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257573 | GAGTCTCGCTCTGTC[G/T]CCCAGGCTGGAGTGC | 286053 |
rs532972826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302913 | CAACTCTGGGAATCC[A/G]GGACAAAGAATCTGA | 286053 |
rs532982747 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340684 | CACTGTGTGTCATCA[A/G]GTAACCTAATCTACT | 286053 |
rs533002459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199873 | GCCTGTGTTGGGTGC[A/T]TATATATTTAGAATG | 286053 |
rs533006774 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251431 | ATTTTTAAATGGGAG[A/C]GACTTGAATATGATT | 286053 |
rs533013963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263726 | CTGCACACCAGCCTC[C/T]GTGACAGAGCGAGAC | 286053 |
rs533016983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237986 | ATCTGATTGATTTTG[C/T]AAATTCCACACCTGT | 286053 |
rs533025286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283964 | GGAGACCATCCTGGC[C/T]AACATGGTGAAACCC | 286053 |
rs533028982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200416 | TGTAAAGGATTTTAT[G/T]TCTCCTTCACTTATG | 286053 |
rs533033736 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159511 | CTATAGAGCCCAGGA[A/G]TGTAGTAGGCTATTC | 286053 |
rs533074228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100141 | AGCTTGCAAAATTTC[C/T]ATTCTGACTGCTTCT | 286053 |
rs533081318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245401 | AATTTGAAATTTAAA[A/G]AAGAAACTTATCTAT | 286053 |
rs533091116 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356333 | TTTTTTGGTTTTTTT[-/G]TTTTTTTTTTTTTTG | 286053 |
rs533103779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354827 | CCTTTCCCTGCCCCT[C/T]AGTACAGCTTGAGCA | 286053 |
rs533110556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347441 | TTGTACAAAATGTAT[A/G]TATTTCACTGATCAC | 286053 |
rs533117675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115862 | AAAGGGAGCTGTCAT[A/G]GCCTACAATAGGCAA | 286053 |
rs533118721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213200 | TTTATTCTCTGTTGT[A/G]AGATTTTCCCCTTTG | 286053 |
rs533119354 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200292 | TTACAGTTTGGCATG[-/T]TTTTTGCGGTGGCTG | 286053 |
rs533123477 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285944 | TCAGGTTTGACCTGA[-/C]CAAAACTTGAGCCCT | 286053 |
rs533138440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310416 | AGAATGTTTGAAAGA[A/G]TACCTACCATATGAT | 286053 |
rs533138710 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333119 | CACTCCAGACCTGCC[A/G]AATCAGAATCTCCAA | 286053 |
rs533143601 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325820 | AACTGGGCATGGTGG[C/T]GGGCACCTGTCATCC | 286053 |
rs533174184 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206254 | GATCAGATCATATGT[A/G]TATGGGAGAAAAGAT | 286053 |
rs533185577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106514 | GAAACCCCATCTCTA[A/C]TAAAAATACAAAAAT | 286053 |
rs533200591 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354073 | AGTAGCTCAGGTTAT[A/G]GGCGCCCACCACCAC | 286053 |
rs533204122 | in-del | -/AC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358502 | AAATATATATAATAT[-/AC]ACACACACACATATA | 286053 |
rs533223130 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353940 | GCTGTCAATTTGTTG[-/T]TTTTTTTTTGAGACG | 286053 |
rs533228427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173891 | GGCAAGATGCTGAAC[G/T]ACTGCGAGCTGCCTA | 286053 |
rs533247077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286520 | GTGTTGCCATGTTGG[C/T]CAGGCTGGTCTCAAA | 286053 |
rs533253798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121015 | TTTTCATCACTATTT[A/C]ATTGTATTTCTTAAA | 286053 |
rs533255035 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233312 | GGTAAATCAGAACCA[-/T]TTTTTGTGATTAATT | 286053 |
rs533261143 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283282 | GGCTAGGCATGGTGG[C/T]TCATGCCTGTAATCC | 286053 |
rs533263959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123260 | TTCTCCTAGACTCAG[A/G]TGTGTTTATAATAAA | 286053 |
rs533264209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350515 | CATGCTGTTGATAAA[A/G]ACATACCTGAGACTG | 286053 |
rs533264243 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342184 | TCTGTGGTTCTACTT[C/G]TGCTCACTCGTAATT | 286053 |
rs533267337 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295542 | GTCGGAATTCTCTTC[A/G]TTGGGCTGCACACCC | 286053 |
rs533275150 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252240 | TGTAAAATAACACAC[A/C]CCTACCGGCCGGGCA | 286053 |
rs533281046 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347903 | ACCTGAGGTGGCAAT[A/G]AATGAAATGCTTACA | 286053 |
rs533283672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303526 | ACTGCTTATTTTGTG[C/T]GAAGTATAATACTGG | 286053 |
rs533313695 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191133 | CGCCTCGGCCTCCCA[A/G]AGCACTGGGATTACA | 286053 |
rs533348898 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317863 | CAGACCAGAATGCCA[C/G]TTAAATTTTTAAAAA | 286053 |
rs533350965 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301770 | TGGGTTCAAGCAATT[C/G]TCCTGCCGCAGCCTC | 286053 |
rs533353816 | snp | A/C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352982 | TCTTCCCCAGTCTCA[A/C/T]TTTTGTTACCTTTTT | 286053 |
rs533355897 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300561 | GTAAGTTGGCACTGT[C/T]CCATTCAACAGTCAT | 286053 |
rs533362974 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-5-prime, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091743 | GGACCTGGAGCGGGT[C/T]AGACCCCGACTTCCG | 286053 |
rs533391093 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192815 | TCCTCACATAGGGGA[A/G]AGGCTTCATCTGTAA | 286053 |
rs533398990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311854 | GAGGCCAAGGCGGGT[A/G]GATTACCTGAGGTTG | 286053 |
rs533402971 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105429 | GTTTTTTTCAGGATT[C/G]TTTTTGAAGATTCCT | 286053 |
rs533405774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152356 | GCTTTCAATTTCAGC[C/T]GAACCCTAGAACCAG | 286053 |
rs533411900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304383 | TAGCAGAGGAGTGAC[A/G]TGATCCATGTAGGTT | 286053 |
rs533425568 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166556 | ACAGGTGTGAGCCAC[C/T]GCGCCTGGCCCTAAA | 286053 |
rs533432351 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147861 | GAACAAAAAAGAATT[-/A]ACGAAAATCCTCTTA | 286053 |
rs533465156 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283297 | CTCATGCCTGTAATC[C/G]CAGCACTTTGGGAGG | 286053 |
rs533480206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252505 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 286053 |
rs533487033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167359 | TTTGTGTATTGAGAG[C/T]TGCATTAAAAGAATT | 286053 |
rs533489111 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117689 | CCCAGCTAATTTTTT[A/T]ATTATTTTTAGAGAC | 286053 |
rs533491589 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115912 | GTTGTGGAAATCACT[A/G]AAAGAGGTCAATATC | 286053 |
rs533493473 | snp | C/T | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090018 | GTAATCTGTTTTGCC[C/T]CATGAAGGGCACTTG | 286053 |
rs533504643 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204146 | TTAGTTCATGTGACC[-/T]TTTTTCCCCCATGGG | 286053 |
rs533519022 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356829 | GCAAAGCATACCACA[G/T]TCTTCATCTCTTTTA | 286053 |
rs533521729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125130038 | GTTGTCTGGGATCCA[A/G]TCCAGGATATCACAT | 286053 |
rs533524446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271673 | TGAATAGGTATGAAT[C/T]AGGTTTCATAGGCAG | 286053 |
rs533565727 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206653 | GGAAAATGGTGATAC[C/G]ATCAAAAAGTTGTAG | 286053 |
rs533566393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230338 | CCTTTCAATTTAACA[A/G]GGCCCTACAATTGTA | 286053 |
rs533570310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173182 | TCAGAATTGCTAGGT[G/T]GCAGTTTAAGCTTCC | 286053 |
rs533586870 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122437 | ACTTACAGAAGGTGC[A/G]TGATGTCACTGGCTA | 286053 |
rs533625437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299302 | AGAAAGGAGCACTCT[A/G]TTCGTTTCTTTTCAC | 286053 |
rs533629240 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176691 | CAGACAGGTGAGCGC[A/T]TTATTGCTTCATTTA | 286053 |
rs533631815 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350828 | GGACACAGCCAAACC[A/G]TATTAGGTTGTCAGG | 286053 |
rs533642550 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210960 | CTGGTCTTGGACCCC[G/T]GGCCTCAAGTGATTC | 286053 |
rs533651243 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162408 | AGAATTAAACCGTTT[C/T]GGCTTTATAATGTAA | 286053 |
rs533657465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362948 | AGGAAGTCCTCCCCA[C/T]CTCACTCTCCACTTC | 286053 |
rs533685751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305713 | ATACCTGCATACTCA[C/G]TTTAGGAGTTTAGAA | 286053 |
rs533701874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | NSMCE2 | GRCh38.p7 | 8:125130258 | GGCCCTTCTCATCAC[A/G]TCATATCAAAGCTAG | 286053 |
rs533710475 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327474 | GTTGTGGGTTTGTCC[C/T]AAATAACTAAAATAT | 286053 |
rs533716611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180618 | AACCAATATCAAGAA[C/T]TTTCTGTATCTAACT | 286053 |
rs533722845 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346057 | AGCTACTCAGGAGGC[C/T]GAGGCAGGAGAATCG | 286053 |
rs533736149 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208378 | ACTGGACTAGATGTA[C/T]AGGAATAGAGAAAAA | 286053 |
rs533737146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327407 | TTATTCATCTGAGTA[A/G]CTGCTGTCTTTTTAG | 286053 |
rs533772818 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178932 | GCCTTAATCCAATAT[G/T]ACTGATGTCCTTAAG | 286053 |
rs533781504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238249 | GCAGGGAACGAGGTT[A/G]TAGAAACTTTTTATT | 286053 |
rs533782094 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305109 | GATGTCTTTATGTTT[C/T]CCAGCTTCAGAGGTT | 286053 |
rs533785787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356243 | GTGTGTATGGGGGGG[C/G]GTGTTCTGGAAATAT | 286053 |
rs533801794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209059 | ACAGATGATCCCCTC[A/G]TCTCAGTCTCCTGAG | 286053 |
rs533804309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222975 | GCTGAGGTGGGAGGA[C/T]CGTTTGAGCCCTGAA | 286053 |
rs533809897 | in-del | -/GA | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243700 | AGCATCCAGATGTGT[-/GA]GAGTCAGGTAAGGTG | 286053 |
rs533815581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201926 | ACCGTCCCCCACCCC[A/G]TTCCCCCGCCTTCCT | 286053 |
rs533817083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272224 | TTTCATTGTGTTAGC[C/T]AGGATGGTCTCGATC | 286053 |
rs533826758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363292 | TGGATCACTTGAGCT[C/T]AGGAGTTCAGGACCA | 286053 |
rs533841318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137542 | GAACTTACTTGATAT[A/T]TTTGTTCTTGATCCC | 286053 |
rs533869939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362537 | TGAAGTGAACTCCCC[A/C]GTCCTTGACACACAT | 286053 |
rs533878307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271844 | TACTTAGCACTTTAT[A/G]TCTTCAAAGAATTCA | 286053 |
rs533885317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278557 | TCAAAGTGCTGACCT[A/G]TTGTTTTAGGTACTG | 286053 |
rs533898337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273073 | GACAGTTACTGCTTC[A/G]TAAATGGTTGCTGTT | 286053 |
rs533923570 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298704 | TTTTTTTTGTTTTTT[G/T]TTTTTTTTCCCCAGT | 286053 |
rs533941481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176276 | TAGTGACTCAAAAAT[C/G]TAATGCACACTTTTC | 286053 |
rs533954990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332591 | TTAGGTTAGTTCTTT[C/T]CTTGTTAAGATTTTC | 286053 |
rs533960285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318488 | TGCAATCTATATATG[A/G]GGAAGTAGCCACCTT | 286053 |
rs533968215 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329573 | GCCAGCAGATCTTAG[A/T]CCTCAGCAACACACC | 286053 |
rs533976930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320163 | TCTGGGCAACAGAGG[C/G]AGACTCCATCTCAAA | 286053 |
rs533978528 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155221 | ACCCAGGGGCAATAA[C/T]GTCTTCAGGGCAGGG | 286053 |
rs533986488 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306928 | TAATAAGTTAATACA[C/T]GTGAAATGCCTAGAA | 286053 |
rs533989682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217030 | CATCCATTTATTCCA[C/G]AAAGATTTATTAAGC | 286053 |
rs533996712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278164 | AGGAAGGAAGCATGG[A/G]TATTTTACATTATTA | 286053 |
rs534002765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173564 | CATTAGCATCATACC[A/G]TCATTGTACTCTTTC | 286053 |
rs534020895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214794 | GGTTTATGCTGTGTA[C/T]ATTTTTATGGGGTGG | 286053 |
rs534039828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312088 | ATTAAAAAAAAAAAA[A/G]AAAAAGAAAGAAAAG | 286053 |
rs534048443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313692 | GTATGTGTTATACAC[A/G]TCCTTAGAGTTTCCT | 286053 |
rs534056489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225322 | CCTTTCATCTTGTGG[C/T]TCTTTTAAGCTCTCT | 286053 |
rs534066463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183251 | TTAAATTGATGCTGA[C/G]ATCTCAAAAAATGAC | 286053 |
rs534068290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106131 | AAACTAACCAAGTGA[C/G]TATTCTGCATATAAT | 286053 |
rs534080011 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311340 | TTTGTAGAAATCTGT[-/A]AAAAAAAAATGCGTA | 286053 |
rs534086641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196562 | CTGCATAGTATTCCA[C/T]GGTGTATATGTGCCA | 286053 |
rs534104157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319016 | CCCAAGGCCAGGGAA[A/G]GAGCTATCTAATGGA | 286053 |
rs534108195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146148 | CTAACAGATTGCCAA[C/G]GGAGCTGAGCTGAGG | 286053 |
rs534116452 | snp | C/T | 0.000819504 | 0.0202257 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222242 | GATTTTTTAAAATTT[C/T]TTAATTGAGAAATAA | 286053 |
rs534136266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239392 | GGTGGGCAGATCACT[C/T]GAGGCCAGGATTTCG | 286053 |
rs534139414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189599 | GCTGCCTAGAAAAAG[A/C]GGGTCAGAACATAGT | 286053 |
rs534152144 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132485 | GACAATTTTTAAATT[A/T]AAAAAAAATTTTGGT | 286053 |
rs534159585 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338551 | CCTTTTCTGAATTTC[A/G]TTAGCAGTAGCAACA | 286053 |
rs534166474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124606 | CACCTCAGTCTCCTG[A/C]GTAGCTGGGACTATA | 286053 |
rs534174661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161116 | AAAAGTTCTTTCATT[G/T]TGCAGTGGAGCCAGT | 286053 |
rs534183988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224507 | TAACAGTCTAATTTC[A/T]TTCTTCTGCATGTGT | 286053 |
rs534204565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286638 | CTTTTATGTGCCATC[A/G]TACACATACATATAT | 286053 |
rs534208574 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256774 | ATTAAAAATACAAAA[A/T]ATCAGCTGGGCGTGG | 286053 |
rs534217437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272812 | ATATATATACACACA[C/T]GTATATATATACACA | 286053 |
rs534236357 | in-del | -/A | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363498 | GAATGAGACCCTGTC[-/A]AAAAAAAGAAAGAGG | 286053 |
rs534237775 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340476 | TATTCCCTTCTCATC[C/T]ATAAATCTGTTGTAA | 286053 |
rs534276300 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320112 | ACCCAGGAGGTGGAG[A/G]TTTCAATGAGCCGAG | 286053 |
rs534287918 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139617 | AAATCATCAGATCTC[A/T]TGAGATTTATTCACT | 286053 |
rs534301043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140508 | TCTCTACTGAAAATA[C/T]AAAAATTAGCTGGGC | 286053 |
rs534307660 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308116 | CACTCCTGTTTGTTT[C/T]CTAGTCTCGGAGGCA | 286053 |
rs534324114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364927 | TAGGTTAGCTTGACT[C/G]CAAACATTGGGCCTC | 286053 |
rs534328605 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228018 | ACATGCACTGGTTGT[C/G]TTTCAGTGGATAGCA | 286053 |
rs534345947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090242 | TATTTGGTAAATAGC[A/C]CCCTCGTTGGCTGAA | 286053 |
rs534356819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345870 | TGCTTAGAAGGCCAT[C/G]GTCAGCCAGGCATGG | 286053 |
rs534356969 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133792 | CAAAACAAAAAAAAA[A/G]AAAAAGAAAAAAGAA | 286053 |
rs534358864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337459 | TTGCTCAATTTACTT[A/G]ATATTGGTCATAGTG | 286053 |
rs534360369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247281 | AAGGCTGCAGTGAGC[C/T]GTGTTCATGCCACTG | 286053 |
rs534367122 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304347 | ATGTGTACTTTACCT[A/G]TGGGAGCCTGTGAAG | 286053 |
rs534410681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104474 | CTCTCTTGATTGCCC[C/T]GAGGGTTCAGTGCGA | 286053 |
rs534420287 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272912 | AAGGCTGTGTAATAC[A/G]GTGGAAAGAGAACTG | 286053 |
rs534431122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246579 | AAAGACTCCTCCCTC[C/T]CCCAAAATGCAAATT | 286053 |
rs534433416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138923 | TAGTTAACCTCTCTG[A/G]GCCTCAATTTCCTCA | 286053 |
rs534437688 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343298 | TATCCAAAAATAGAC[A/G]TCTTCAGAGGTTCTT | 286053 |
rs534454594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152833 | GAGGCCGAGGCAGGC[A/G]GATCACCTGAGGTCA | 286053 |
rs534471248 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110605 | AGGTCACAAAGTTAG[G/T]AAATGTTTGAGTAGG | 286053 |
rs534483607 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352125 | AAATAATGTATATGA[C/T]GTGCTTAGCACTGTA | 286053 |
rs534483858 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239999 | CTTTGTTTTCTCTTT[A/C]CTACTGTTGAGGGTC | 286053 |
rs534487303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279481 | GTTAAATAAGAGTAC[C/T]AATTAGAAGCAATTC | 286053 |
rs534507098 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240149 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 286053 |
rs534508612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307488 | AGACCCTAGTTGATA[C/T]ATCTCCTGAGCCCAT | 286053 |
rs534514143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336278 | AATTACTCAATTAAA[C/T]TCAATTCAATACTCA | 286053 |
rs534521052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358234 | GCTACTCGGGAGGCT[C/G]AGGCAGGATAATCTC | 286053 |
rs534522970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145392 | TGTGGGGTGGCAGTG[C/T]GGGGGGGATAGCTAG | 286053 |
rs534523803 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111664 | AATTAGCTGGGTGTG[A/G]TGGTGTGTGCCTATA | 286053 |
rs534524716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328748 | ACCTTTTCATTCATC[C/T]CTGTCATCTGGGTCT | 286053 |
rs534554441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191565 | CACTTGCATTTAGAG[A/G]TTAGGGAGTAGTAAT | 286053 |
rs534558000 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132385 | GCCTCTGTGCCTGAC[C/T]TGTTCATATTCTTCT | 286053 |
rs534562759 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275505 | CCACTGAGTTCTCTT[C/T]CTCTTACTGCCCTCT | 286053 |
rs534567154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330320 | AGCTGGAATTACAAG[C/T]GTGTGCCACCACACC | 286053 |
rs534579932 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282536 | ACCTCTGCTCCACTT[A/G]CTCCTTCGATTTAAG | 286053 |
rs534582570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249216 | GTGAAATTCAATCTT[A/G]TACCAGAGTCCACTT | 286053 |
rs534591621 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235585 | ATGGAGTTATATTTT[A/G]TACACATATACAATT | 286053 |
rs534606987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210253 | AGTGTCTTGGCACAC[A/G]GTAAATGTTATGTGT | 286053 |
rs534608748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287679 | AGAGAGAGATTGTCC[C/T]GTGTCTAGCTAATGC | 286053 |
rs534614702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184644 | GATCTGTATACCTTA[A/C]TTGCAAAATGTAATT | 286053 |
rs534648114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301034 | TATTTCTGTGTCACA[A/G]TCATTAACTATTTTT | 286053 |
rs534653685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141128 | TACTTTATTTCAAAC[A/C]GTATTTTGAATTATA | 286053 |
rs534657079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155361 | CTTATTTCTGATTGT[C/T]TTGATGTCAGCTTCA | 286053 |
rs534695748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157277 | TTCGAGCCAGAGGGG[A/T]AAGTACTAGGAGACT | 286053 |
rs534696643 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226076 | TCTGTTTGCAAAAAA[G/T]AATACATACAATTTT | 286053 |
rs534698879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247542 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 286053 |
rs534703640 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302430 | ATGAGTGAGGGAAAG[G/T]AAAGTAGGAGATGAG | 286053 |
rs534716160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353681 | CAAGGTCAGGAGTTC[A/G]AGACCAGCGTGGCCA | 286053 |
rs534735239 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353299 | TTACTCTTAAACACA[C/T]GATCAGAAATGGGAG | 286053 |
rs534750786 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142086 | CCTTTTGGTTCCAAA[-/G]GCAAAGTGCTTTCAG | 286053 |
rs534752896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288125 | GCCACCATACTGGCC[A/G]ATGTTTTAGGATTCT | 286053 |
rs534767539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262036 | CAGGAGGTGGAGGTT[A/G]CAGTGAATTGAGATT | 286053 |
rs534767908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118435 | CCTTGCCACTAGAGT[C/T]TCAGTAGGTCTCGAA | 286053 |
rs534769150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288962 | ACCACCATGCCCAGC[C/T]AATTTTTTGACTTTT | 286053 |
rs534783349 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270354 | CCTGTAAACCCAGCT[A/C]CTCGGGAGGCTAAGA | 286053 |
rs534796381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257626 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 286053 |
rs534799025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162873 | AGATTCACATTTACC[A/T]TTTGACTTTAGTCAT | 286053 |
rs534810227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300404 | CTGAACTCAAGTGAT[A/C]CTCTTGCTTCAGCCT | 286053 |
rs534812587 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225691 | TTATTTCTTGATATA[A/T]TTTATAAGAAAATGT | 286053 |
rs534814003 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217562 | TAATAGAGACAGGGT[G/T]TCACTGTGTTAGCCA | 286053 |
rs534834502 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271489 | ATACCTAGGTATTAA[G/T]GGTACATAGGACTGA | 286053 |
rs534843380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261174 | TTGTGGAATTGTTCA[A/G]AGTTTATTGTTTAAC | 286053 |
rs534843588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295651 | TTCATAATACATCAT[C/G]CCATGTTCTGCCTCA | 286053 |
rs534880607 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255712 | CCAGGTGAAGACATA[C/T]TGTGTACACACAGCT | 286053 |
rs534891988 | snp | C/T | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091491 | AAGCCCCTAAGCCCT[C/T]CATCCCGAGTCCCCC | 286053 |
rs534893658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127336 | TGGGGGAGTACATGA[C/T]AGTAAGGGCCATGTG | 286053 |
rs534908617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170921 | AAATCAGAGGTTTTT[A/G]CTACTCTGTGCAAAA | 286053 |
rs534912301 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366323 | AGGCGGGCGGATCAC[C/G]AGGTCAGGAGATCGA | 286053 |
rs534918227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127322 | ATGTGTGCTGAGGTT[C/G]GGGGAGTACATGATA | 286053 |
rs534926991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275364 | TATTCATTATAATTT[C/G]TGGTTAAAAACTATC | 286053 |
rs534933329 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135517 | ATTTTGTAGTTTTAG[A/G]TTTTGTATTTAAGTC | 286053 |
rs534943795 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279511 | CAGTAGACTGGGGTA[A/G]GTAAGGTCAAGTCTG | 286053 |
rs534954465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162083 | ACATGAAATACTAAA[C/T]AGGAACTTTAAGTGG | 286053 |
rs534956509 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093958 | CAAGCCACTATGTCT[C/G]TGTAAGTTTAAATTT | 286053 |
rs534961521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221079 | CATGGTCATACCCAC[C/T]CTCTACTGCTACATT | 286053 |
rs534988222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134250 | TATGAAGACTTCTGA[A/G]TCATTATGATGAGAT | 286053 |
rs534988801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354116 | TTTGTATTTTTAGTA[C/G]AGAAGGGGTTTCACC | 286053 |
rs535021950 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359279 | TCCAAAAAAAAAAAA[A/C]AAAGAGGGAGGATTC | 286053 |
rs535031647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218450 | AGAGTCTTGCTCTGT[C/T]GCTCAGACTGGAGTG | 286053 |
rs535048310 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251242 | AAGTTTCAGGGAGAC[A/G]CAGGGAACAGAATAA | 286053 |
rs535060820 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146357 | GCCTTGAGCAAGTTA[C/T]TTCAGTTTTCTCATA | 286053 |
rs535080719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171530 | TATTTGTTTGGGGGA[A/G]GGTTAAATAAAATAA | 286053 |
rs535092183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296071 | TTAATTAAAAAAAAT[A/T]GCTAGCACTTATTAA | 286053 |
rs535100504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347520 | TTCCTCTTTGTATCT[A/G]TACCTGGAATTTGGT | 286053 |
rs535103872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338939 | TAAATTCACGCTCTG[C/T]CCTAGATTTACAGTT | 286053 |
rs535106159 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191989 | AAATGACAGATAGCT[A/G]TAATTAAAGTTAGTG | 286053 |
rs535107987 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218451 | GAGTCTTGCTCTGTC[A/G]CTCAGACTGGAGTGC | 286053 |
rs535120321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270736 | AAGTTCAGCATCAAT[A/G]TGGTGACCCCTCAGG | 286053 |
rs535134070 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144148 | CTCTGGGTACCATGT[A/G]CTACCGGACCTGTTT | 286053 |
rs535134615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311396 | AAATCTCCAAAGAAG[A/G]AAATCTTATTTTTAC | 286053 |
rs535136773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303790 | GATGAATGATTCCCT[C/T]AGTTGCTCTCAGCTT | 286053 |
rs535145228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164564 | GTGGCGTGTGTTAGA[C/G]AGGGATTCTATTAGA | 286053 |
rs535147096 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300104 | GATTACAGGCATGAG[C/T]CACTACACCTGGACA | 286053 |
rs535148193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316903 | TGCACCTCAGCCCCC[C/T]GAGTAGCTGGCACTA | 286053 |
rs535151151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302935 | AGAATCTGAGCACAC[A/G]TCATGCACCACACAC | 286053 |
rs535152980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187642 | CTGTTACGTGACTAT[C/G]AGGCCCTGTAGATTT | 286053 |
rs535153015 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116935 | CTCTGTCACCCACTC[C/T]GGTGGGCAGTGGCAT | 286053 |
rs535177846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275865 | AAACCCAGAACGCTC[C/T]GCCTGCAAAACCCAA | 286053 |
rs535194933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310783 | TTTTTCCTCCATGCT[C/T]ATTTACCGAGGAGTA | 286053 |
rs535200797 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357091 | AGAAGAGTTTCTATG[C/T]ATCCAGTCCTTACAT | 286053 |
rs535203008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324048 | ACAGACACTTAAAAT[A/G]TATAGATGACAAGCA | 286053 |
rs535212172 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119503 | TTAGGTTTCAGTGGC[C/T]TAACAGGGTTTGAAA | 286053 |
rs535238296 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172326 | TCTTACTGCAGTGCA[A/G]TATCACTCCTAAAGT | 286053 |
rs535272063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211972 | ATGTACTTGTCAGAC[C/T]AGGTATCCTCATTTA | 286053 |
rs535280433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289403 | CTGTCTCTGCTCTCA[A/G]TCTGCCCAAGTCCTG | 286053 |
rs535285314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218951 | CTATATAAGGACTCC[A/G]TTTGGTCTCTGCAGA | 286053 |
rs535292393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309116 | GTTGGGCATGGTGGC[A/G]CATCCCTGTAATACC | 286053 |
rs535311459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185208 | GGGCAGGCCTAGGTA[C/T]ACTCTGCTGGCAGTG | 286053 |
rs535319056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269962 | ATGCAAGGCTGAACT[A/G]AAGGACAAGCACGGC | 286053 |
rs535328448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157953 | GATTAAAAGAATTTC[C/T]TTAAAGACTCCAAAG | 286053 |
rs535330065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243725 | TAAGGTGGAGTGAGG[A/G]AGGCGATAGTTATCT | 286053 |
rs535347359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283655 | AGATGAAATGCAATT[A/G]TGTATCAAGACACAT | 286053 |
rs535349792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227583 | ATTGCAAATGTATTG[C/T]AATTCATATTAAAAA | 286053 |
rs535361220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308720 | AAGCCATTTTCCTCC[C/G]CTTTTTCAAGCCACA | 286053 |
rs535371601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276692 | GGTGGATTTGGCACA[A/G]GTATTATACTATATA | 286053 |
rs535375037 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180167 | AGGATAGCTAGTCAC[C/T]GTGTATAATAGCTCT | 286053 |
rs535375115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193326 | ATCTTACAAAGAATA[C/T]AGTATATCCAGACTG | 286053 |
rs535382819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271282 | AAAAAAAAAGTATTA[C/T]TCTAGTGATGAGGTA | 286053 |
rs535383986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150163 | TGTTCTGCTTCATGG[C/T]CAAGGCTAACCTCCC | 286053 |
rs535392305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325718 | ACACTTTGGAAGACC[A/G]AGGCAGGAGGATCAC | 286053 |
rs535406841 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129200 | ATGACAAGAAGGCCC[A/G]GGCCAGTGTCCTTAG | 286053 |
rs535411580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121303 | CAAGACAAAGATTTG[C/T]GCTTCCTCTTCTTTT | 286053 |
rs535414713 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334597 | GGAATTGTTTTTCTC[A/T]CGGGTTGGAATGTAG | 286053 |
rs535418043 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091975 | TAGGGAAGAAGCGGG[A/G]GACGGCAATGGGGAG | 286053 |
rs535423071 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126493 | TGCATGTTAACTTCA[G/T]GTTGGGCCTTTCCAA | 286053 |
rs535429382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229407 | ATTTTTAATATTTTA[A/T]CCTCCTTTCCAGTGG | 286053 |
rs535433346 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238318 | ATAGCATTTCAAAGG[G/T]TTTCAAGTTCCATGT | 286053 |
rs535434309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172912 | TTTATCTGACAACAC[G/T]TTAGACTGTCATTCA | 286053 |
rs535455203 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277327 | AGTCACCTCTCTGAA[A/G]TCAAGGCCATGATAT | 286053 |
rs535466977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145088 | ACTCTAAAAAGAAAC[C/G]CCCTCCTTCAGTGAT | 286053 |
rs535472068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213772 | AGAGACCTGGAGGTC[G/T]CCAGGCTACCCATTC | 286053 |
rs535472572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121952 | CCTTACATATTCTCA[C/T]CCATCATCCTTTGTA | 286053 |
rs535491095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237575 | AAACTGCCTTTTCAA[A/G]GAGATAATTCACTAT | 286053 |
rs535499771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188871 | GGGAGCCCCCTCATC[C/G]AGATGCAGGTGAACA | 286053 |
rs535502214 | snp | A/G | 0.000186898 | 0.00966511 | intron-variant, synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125130317 | CAACCTTGATCACCT[A/G]GCCCTAGTAGTGTTT | 286053 |
rs535506706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231841 | TCTACCATGCACCTC[C/T]TGAAAGAAGGAACAC | 286053 |
rs535511698 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252587 | TTCTTGCATTTGACT[A/C]TCTCAAAAATTGGCA | 286053 |
rs535527680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138248 | TCTCTTTTAGAGACC[A/T]GGTCAATCTCTGTCA | 286053 |
rs535543894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362387 | GAAGTCTTCCCTGAG[A/C]CCTTATTCATGCTGG | 286053 |
rs535567886 | in-del | -/AA | 0.231225 | 0.249294 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247725 | CAAAATTCTGTCTCA[-/AA]AAAAAAAAAAAAAAG | 286053 |
rs535569317 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239310 | TATGTTACAAAAAAA[G/T]AGCATTTTAAAAATT | 286053 |
rs535575031 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147162 | GTTGTGTGATTTCTA[C/G]CCACCACTCCAGTGC | 286053 |
rs535576126 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293032 | GGGGGCCTGGTTTAG[A/G]TCTGATACCATATGC | 286053 |
rs535580712 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242547 | AAAACTTGGTTCCAG[C/T]AAGAACTGTTAGCTT | 286053 |
rs535586397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193857 | ACAGTGAGAAGCAGC[A/C]TCATAATTACCCTTT | 286053 |
rs535602444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332577 | AAACAAACAGGTTCT[C/T]AGGTTAGTTCTTTCC | 286053 |
rs535615972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207417 | CAAAGCTAGCAATTA[A/C]TTTTTATTTAGAAAT | 286053 |
rs535616407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244090 | TTAACAGAGTGGTGT[G/T]CCATAAAGCTAATGA | 286053 |
rs535617859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200812 | CTTTCAGCTACACCA[A/G]TCAAACGTAGGCTTG | 286053 |
rs535629017 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289208 | CTTCCTAGAGTAATC[A/C]GAACACATGAAAAGC | 286053 |
rs535635890 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328347 | TCCATTTAAGAATCA[A/G]TTTTCATGCCTGTCT | 286053 |
rs535642278 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284238 | AAGTTCTGCCACTTT[C/G]TTAAAAAAAATACCC | 286053 |
rs535642888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251953 | TTAGACTTTTTAACA[C/T]GCTGGATCTAAGAGA | 286053 |
rs535648803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304467 | CCCGGGGCAAGGAAA[C/T]GAGACAGCAAGTAGT | 286053 |
rs535659005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100880 | GCTGAATATTTCTAG[C/T]GCCTGGGATAGTGCC | 286053 |
rs535668992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297120 | TGAATTCGTAACATC[C/T]CTGTCATAATCACAC | 286053 |
rs535670297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328545 | CTGGTTTCAGAATTC[A/G]CTGCCAAGCCAGAGG | 286053 |
rs535677278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348438 | TCCGTCTGAATTCTG[C/T]GAAATGTCTTCACAT | 286053 |
rs535681725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250985 | ATGATCCTATTTTTA[C/T]AAAATATATTTTAAT | 286053 |
rs535688755 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108242 | AGAGAAAGCCAAGGG[C/T]AATCACTCCCACTGG | 286053 |
rs535693388 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339995 | ACCATAAGCCTCCGA[C/T]GTTGTAGTTTTTTTT | 286053 |
rs535696905 | in-del | -/AT | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272876 | TATACACACGTATAC[-/AT]GTGTGTGTATATATA | 286053 |
rs535699567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228777 | ATAATCAATTCATAC[A/G]TGCCTGGCTCTGTGC | 286053 |
rs535714231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315435 | TTCAAATCACACTGA[C/T]TTCTTGTATTAGCTG | 286053 |
rs535722372 | in-del | -/TAT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324049 | CAGACACTTAAAATA[-/TAT]AGATGACAAGCACAT | 286053 |
rs535725313 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106617 | TTGAACCTGGGAGGC[G/T]GAGGTTGCAGTGAGC | 286053 |
rs535734580 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265917 | CCTGTAAATGTGTAT[C/G]ATGAACCCTCTATTA | 286053 |
rs535746887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206666 | ACCATCAAAAAGTTG[C/T]AGACTGTCTCATGGA | 286053 |
rs535751312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351132 | AACTCGGTGGATGCT[A/G]ACTGAGAAGAGGAGA | 286053 |
rs535759324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157708 | TGCTAATAGGTGAAG[A/G]TATGTTATATTGAGA | 286053 |
rs535763472 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236841 | TTTTCTGATCTTGCT[C/G]CTTTGCTAGACTCTT | 286053 |
rs535776055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214516 | TACGTGAAAGAAAGG[A/G]GTTTGCCACAGACCA | 286053 |
rs535782031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099701 | TTGACAAGAGCAGTT[A/G]CAGTGGAGTGATAGA | 286053 |
rs535795779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188365 | TGTAGTATTACCATA[A/G]CACAGGTCCTTGATG | 286053 |
rs535799805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166625 | AAGAAAACAATTCAC[A/G]TTTTCCTGTCTTTCT | 286053 |
rs535830253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110689 | TCATAAAAAATGTAT[C/T]GTGCCAGCGTCATGG | 286053 |
rs535867023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181036 | ACAATAGAGAGTTTG[A/G]TGAGTTTTGCTTGGC | 286053 |
rs535916792 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286316 | AATACCTTTTATTTA[A/T]TTTTTTTTTTTTTTG | 286053 |
rs535937318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278684 | TTTGGTCAAGAGGGT[C/T]TTCTTTTTTCTTTCT | 286053 |
rs535938461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293223 | GCTGCCCCACCTTGC[A/C]CTCTCAGGGATCTTG | 286053 |
rs535948088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344052 | TTAAGATAATACATC[A/T]AGAAAATACAAGGGA | 286053 |
rs535961559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116988 | CACCTCCTGGGTTCA[A/G]ACAGTTTTCCTGCCT | 286053 |
rs535965216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327528 | ATTAAAGTAAGAGAG[C/T]GTTTTTTTTTAAGTC | 286053 |
rs536000656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107355 | CACACCACCATGCCC[A/G]GCTAATTTTTGTATC | 286053 |
rs536003304 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285502 | GTATATACCCAGATA[A/G]GAATAGGGTAGCCAT | 286053 |
rs536027498 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258900 | TCTGGCCTGCTCACA[A/G]AGCTTTGTTTTCTGT | 286053 |
rs536035073 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207446 | ATTTTACTTTAATCA[C/T]AATTTGATTTTTAAG | 286053 |
rs536039971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319936 | AATCTAGCACTTTGG[A/G]AGGCCAAGGCTGGCA | 286053 |
rs536042610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102032 | TTTAAGAACTGTGCT[A/G]TTGTTGACTTCTTCA | 286053 |
rs536058255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355508 | AGTTCAAGACCAGCC[C/T]GGCCAATATGGTGAA | 286053 |
rs536062585 | in-del | -/G | 0.0658909 | 0.169127 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356236 | ATGTCTGTGTGTATG[-/G]GGGGGGGGTGTTCTG | 286053 |
rs536076725 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094900 | GCTCTGTTGCCCAGG[A/C]TGGAGTGCAGTGGCG | 286053 |
rs536084406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264942 | TGTTAGTACTATACA[A/G]ATGAGAAATCTCAAA | 286053 |
rs536086445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258115 | GGGCAGTCTTTTGGG[A/G]TACAGTAAGTGTGGG | 286053 |
rs536086668 | in-del | -/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301671 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCCC | 286053 |
rs536107287 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294650 | CTGGATTGACTTTCT[A/G]AAACAAAACCATAGT | 286053 |
rs536111503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166145 | AGACTTACTATTTAT[C/T]AGAAAAGTCATGGCA | 286053 |
rs536129859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259889 | AGATCTTCTGACTTC[C/T]AGCTCTTTTCAGCTA | 286053 |
rs536135669 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142003 | GTGAGTTCAGTTTCA[A/C/T]GCTTTAGAAGTTAGT | 286053 |
rs536135835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357036 | GTTTCCTTATCAAAA[A/G]TAGTCAGAATGAGGT | 286053 |
rs536138754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114992 | ATTTTATGTTTCTTT[A/G]TGTGTCATATTTCCC | 286053 |
rs536147065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266809 | CTTAGTAAAGGAAGT[C/T]GGAGGCAAGGAAACT | 286053 |
rs536150128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130865 | AACTGGACTCCCACC[A/G]TCCACTGTACATTTG | 286053 |
rs536151068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252344 | CCAACCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 286053 |
rs536173049 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356328 | TTTTAATTTTTTGGT[G/T]TTTTTTTTTTTTTTT | 286053 |
rs536173645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312922 | GAGCACAGAGAAGAA[C/T]TCAGCAAATACACAG | 286053 |
rs536181690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297725 | CTGTAGTCATAGCTA[A/G]TTGGGAGGCTGAGGT | 286053 |
rs536189147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158713 | TGTCAATTTAACTTC[A/C]TTCCAACCTCACAAT | 286053 |
rs536207005 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197703 | CCATGTGAACTTTAA[A/C]GTAGTTTTTTCCAAT | 286053 |
rs536218244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343509 | CCAGGCGTGTTGGCA[C/T]GCACCTATAGTCCCA | 286053 |
rs536234832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299410 | ATAGCAGAAGGTAAA[A/G]AGCAAGCAAGGAATG | 286053 |
rs536255787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169715 | GCCCACGAGATCTTT[C/T]TAAAGTGAACATTTG | 286053 |
rs536267397 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196677 | ATGTGTGCATGTGTC[A/T]TTACGGTAGCATGAT | 286053 |
rs536271966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365425 | CCTGCAGGATCCCCC[A/G]TGCTATTTTCCCTGC | 286053 |
rs536278781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202690 | TTTTGAACTTATTAG[A/G]GGCATTTACTTTAAT | 286053 |
rs536286033 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210890 | TATGCCACTATGCCC[A/G/T]GCTAATTTTTTTTGT | 286053 |
rs536299798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308404 | CCTAATGGTCTTCTT[A/G]AGTCAGAGAAGTCTT | 286053 |
rs536301487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301177 | AGGATTGGCTGGGGA[A/G]TGTGCTAGAACCCCA | 286053 |
rs536316548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160474 | TGGGGGTGGCTTGGG[A/G]TATGGAAGTTAGTGC | 286053 |
rs536328048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176346 | ATCTCGAAATTCCTT[C/T]CTAAACTTTGTGGAT | 286053 |
rs536328182 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131962 | CAGAGTCTATGTTAA[C/T]AACATTGTAAAAGCT | 286053 |
rs536335574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262147 | ATAAATTGTATAGGC[C/T]GGGTGCGATGGCTCA | 286053 |
rs536345776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247454 | GTGACCAGTTAAGAT[A/T]TGGCTCACGCCTATA | 286053 |
rs536354991 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181832 | TTCCCTGGCAGTTAT[A/C/T]AGAAGACAACAAGTT | 286053 |
rs536365058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307645 | AAGAGGAAGCTACAG[C/G]GTTGTAGGCTTGATA | 286053 |
rs536373678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217620 | ATCCACCTGCCTTGG[C/T]CTCCCAAAGTGCTGG | 286053 |
rs536374167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292312 | GTAATCCCAGCACTT[C/T]GGGAAGCCAAGGTGG | 286053 |
rs536386869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300135 | ATTTTCGGCTTTCTT[A/G]TACTGGAAGTGGGTC | 286053 |
rs536388553 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135241 | ATTTTTTGGGGGACA[A/G]GCTCTCTCTATATTG | 286053 |
rs536399692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190756 | TCATAGGCATGCTTT[A/G]TATAATGCCTAGTAC | 286053 |
rs536419510 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166711 | GGACCCAGGGAAGAC[A/G]CTTCTGCTACCATCT | 286053 |
rs536456499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286713 | ACTTGCTTAAGCTTC[C/T]CTAAGCCTTGTTTAT | 286053 |
rs536465239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183359 | AGACTTTTGTTTTTA[A/C]TGTAGACTTAACCAG | 286053 |
rs536469755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272260 | ACCTCATGATCCGCC[C/T]GCCTCAGCCTCCCAA | 286053 |
rs536477596 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116314 | ACACAGGCTCATACA[C/G]TGCTCACCACAGGTC | 286053 |
rs536486693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208423 | AGTCTTTACTTTCAA[G/T]AAGTTTATATGCTTA | 286053 |
rs536489179 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247907 | TGGTGAACTAAAGTG[A/G]CCACTTTCCTTGTGA | 286053 |
rs536489521 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319162 | AGAAAAAAATTAACC[A/G]TAGATTAAACACCAC | 286053 |
rs536490991 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132548 | CCCAGGCTGGAGTAC[A/T]CTAGTGCAGTCTCAG | 286053 |
rs536505048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305863 | CCTCACAGAGCTTAT[A/G]GTCTAGTGGAGAGGC | 286053 |
rs536506344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146459 | CACATATGTTTATTG[C/T]GGCACTATTCACAGT | 286053 |
rs536508609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154259 | GAATTTATTATTTAA[A/G]TAGACATCTCTCTTC | 286053 |
rs536532845 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181591 | TAGCCTTGAACAGAA[A/C]CAGGGGGCACTTATT | 286053 |
rs536535975 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197296 | GTCCTGAATGGTATT[A/G]CCTAGGTTTTCTTCT | 286053 |
rs536565858 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305138 | TTGGATAAATGGAGA[C/T]ATTAAATTAACTGGT | 286053 |
rs536572787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146847 | CACATGTATACATAT[A/G]TAACAGACCTGCATG | 286053 |
rs536597812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280388 | TGTCCTTTCTAAAAC[A/T]TTTACCTAAAATGTT | 286053 |
rs536619414 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360408 | GCCAGCAAGGCAGGA[C/T]CCGCACCTCGCCTGT | 286053 |
rs536619519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117890 | TTGTGTTCTCTTAAT[A/G]CAAATATCTGGATCA | 286053 |
rs536624594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134302 | TAAATTATATAGTTA[A/C]ATGTACTTTTTTAGT | 286053 |
rs536637432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226244 | CTCATGGCCCAGTCA[C/T]TGTGTAGATTTGCTT | 286053 |
rs536664991 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091865 | AGAGCCCGCTCTCAC[C/T]TTTCAGCGGCAGGCG | 286053 |
rs536690832 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243019 | TATTGGTTACATGTA[G/T]ACTCTATCTGGGTAA | 286053 |
rs536695956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331118 | CATCCTGGCCAACAT[G/T]GTGAAACCCCGTCTC | 286053 |
rs536702325 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227679 | ATTCCTTTATATTCA[A/G]TCTGTTTCGAATTAC | 286053 |
rs536719505 | snp | G/T | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093778 | GTTTTCTCATGGTGG[G/T]AGCAGGATGAGGAAA | 286053 |
rs536723257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287835 | GAATATCTCCAGTGA[C/T]CTGCACATTGCCAGT | 286053 |
rs536729360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184245 | GTTATTATTCCACAA[A/G]GTAAAGGATGAAGAC | 286053 |
rs536732591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192340 | AAAGGTTTTTTTTTT[A/T]TTTTAAAGAAAGTTT | 286053 |
rs536733932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199211 | CTGAGTTATTTCTTG[A/C]CTTCTGCTAACTTTA | 286053 |
rs536739119 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359082 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGACT | 286053 |
rs536739916 | snp | C/T | 0.000643676 | 0.0179283 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125366876 | GAAAAGACATCGTCA[C/T]TCCGAGTAGGAAAAG | 286053 |
rs536742735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098386 | ATTGTCAGTTATTAC[A/G]AAGCTCTTTGGCCAT | 286053 |
rs536757251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097888 | TTTGGATACTGTGCT[A/G]ATTATGTTGAATTTT | 286053 |
rs536761398 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304808 | GATGAGAATCGCTTG[A/T]ACCCTGGAGGCAGAG | 286053 |
rs536765836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227179 | CCCATCCTCAAATTG[A/G]GGGGCAGCCTCCAGA | 286053 |
rs536766843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141174 | TTTATAGATATTAAC[A/G]TACATTCTAAGGATA | 286053 |
rs536780517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098835 | AATGTGGGCCTTCCA[C/T]GTTGGACGTTTTAAG | 286053 |
rs536782867 | in-del | -/A | 0.330249 | 0.23677 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154512 | AGTGCTCTGAAAGTT[-/A]AAAAAAAAAAAAAAA | 286053 |
rs536792373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185244 | GCTGTAAGTTAATCT[A/G]TCTGTGGCTCAGCAG | 286053 |
rs536795812 | snp | C/T | | | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125099473 | AGAAGAAAAAGAAGC[C/T]TGGATTCTGAACCTG | 286053 |
rs536811390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198254 | TGAGAGAGGGCAGCC[C/T]TATCTTGTGCCGGTT | 286053 |
rs536820224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345984 | AACATGGCAAAACCC[C/T]GTCTCTACTAAAAAT | 286053 |
rs536839752 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301545 | TCTTGTTAGTTGTTA[A/G]GAGACAGCGTCCCAG | 286053 |
rs536897729 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234050 | TACAAAAAATTAGTC[A/G]GGTATGGTGTCAGGC | 286053 |
rs536898061 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225472 | TCTAAGTTCCTGAGA[G/T]AGCTGCAAAAAGAGG | 286053 |
rs536900796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140433 | TTTGGGAGGCCAAGG[C/T]GGGAGAATTACTTGA | 286053 |
rs536905401 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307051 | ATGGGAGCCCAGCCC[A/G]TTGTAAATCACTCAC | 286053 |
rs536910517 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365038 | AGAGAAGACCACATC[A/G]AAGCAGAGCCGTGGC | 286053 |
rs536913261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288287 | TCTCTGACTGCTGGG[A/G]CGTAACAGGAGGCCC | 286053 |
rs536913716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170628 | GGCCAGGCTGGTCTC[G/T]AACTCCTGACCTCAG | 286053 |
rs536915276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162972 | CAGTTCAACAAGTGA[C/G]TGGTGTAGACTGGGC | 286053 |
rs536940367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103661 | AGTGGAACTTGATAG[A/G]TTTTTTCCAGTCTTT | 286053 |
rs536942044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189623 | ACATAGTTAAGGCAG[C/T]CTGATGATAAAAATC | 286053 |
rs536943287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111737 | CCCAGGAGGCAGAGG[C/T]TGCAGCGAGCCGAGA | 286053 |
rs536954785 | snp | A/G | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363127 | TTCAATGTCATGGAA[A/G]CCAAAGTTATGATAC | 286053 |
rs536956103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321438 | CAGGCAACTGGCTTC[A/G]TGGTGAATTCTACCA | 286053 |
rs536977405 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096415 | AGTTTGCTATTGCAT[G/T]TACTATAAGGATATT | 286053 |
rs536989883 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240655 | GGCAATTTTACCATA[A/G]GGCTTGATAGCATTA | 286053 |
rs536994920 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261073 | GATATTTACATTTCG[C/G]TGAAAAGGGGGAGAA | 286053 |
rs537011975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251119 | TTCTCTAGTAAAAGC[A/G]TAGTGGTTCCATAAT | 286053 |
rs537012660 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285039 | TGAAAAGGATTCTAA[A/G]TATAGTCTGAATTAG | 286053 |
rs537018905 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235983 | CAGATTTCTATTCCT[A/G]GAAATATGGCAGTTA | 286053 |
rs537025546 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340022 | TTTTTGTTTTTTTTT[G/T]TTTTTTTTTTGAGAC | 286053 |
rs537026623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142134 | CTTGCAGAATAGTTA[C/T]CTATTCTGTAATAAT | 286053 |
rs537031274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243528 | CCTCTAAATTTCTAA[C/T]GTGTATTGTCATTGA | 286053 |
rs537033139 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331173 | GACTTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 286053 |
rs537042445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150223 | TTTTGGTTCATCTTT[A/T]TACAAAGAGTTGGGA | 286053 |
rs537042458 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270797 | GGTGAACGGGCCCAG[G/T]TTGAAAATGGAGCAG | 286053 |
rs537045951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158478 | ATGGGCAGGAAACGC[A/G]TATGGACCTTTGAAG | 286053 |
rs537051991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288843 | AGTCTCGCCCTAGCT[A/G]GAGTGCAGTGGCTCG | 286053 |
rs537053156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177976 | CCACATTAAATATCT[G/T]GGAGGCATCATTACT | 286053 |
rs537059763 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185849 | GTCAATCTCTTCAAT[G/T]TTTGGCTTATTTAAA | 286053 |
rs537060349 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347664 | TTCCATTCACATGAA[A/G]CAACAGAATAAGAAA | 286053 |
rs537098588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338821 | GAAACTGAATGATTA[C/T]GGAAAAGGTTTCTTG | 286053 |
rs537115547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283255 | CACTGAACTTAGAAT[C/T]AGGAGATCTGGGGCT | 286053 |
rs537131633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228605 | GGCATTTGAGGCTGA[A/G]AGTATAGTACATTCA | 286053 |
rs537143314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114048 | ATTCTCAAGAAGTTA[C/T]CTATAAGCACATGAT | 286053 |
rs537151148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251664 | CACTTATTGGATGCC[C/T]GTTATGTCTTAGACA | 286053 |
rs537163406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149131 | ATTTTGTTAAACATA[C/T]ATTTAATTTGGGGAA | 286053 |
rs537181685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282316 | CCGGGGTTTCACCAT[C/G]TTGGCCAGGCTCGTC | 286053 |
rs537190946 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274247 | GAAAAATACAGAAAA[C/T]GAAACAAAAAAAAAC | 286053 |
rs537200716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263497 | GCTCATGCCTGTAAT[C/T]CCAATACTTTGGGAG | 286053 |
rs537207270 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356025 | GGTCAAAACTGTCTT[C/T]ATAATAATAGTATGA | 286053 |
rs537208021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112183 | CATTATAACTTAAAT[C/T]AGTGAAGATTATTAA | 286053 |
rs537217316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125127807 | ATTTACATATACATA[A/G]TGAGATACCTTGGGG | 286053 |
rs537221167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212433 | GAGGCAGTGAGAGCC[C/T]GGTATGTGCAGGAGG | 286053 |
rs537227706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309278 | AAAAAAAAGAATTGT[A/G]TTGTGAAACCACAGA | 286053 |
rs537236455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147921 | TGGACGTTCTCATGA[C/G]CTGTCTTTAAGATGC | 286053 |
rs537255779 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105075 | GGAGGCCATTGCAAG[A/G]CTTTTCCCAGTTTTC | 286053 |
rs537260932 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153035 | GCACTCCAGCCTGGG[A/C]GACAGAGCGAGACTC | 286053 |
rs537263585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345202 | AATACGTATGTGGAG[C/T]AGTTTATTTCTTCCA | 286053 |
rs537268896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255450 | TCATCATCAAGGAAG[A/C]CTCCCTCAATGAATG | 286053 |
rs537269721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360129 | TAATACTGTCATTTG[C/G]TCATTAGCCTCCAGA | 286053 |
rs537279593 | snp | G/T | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090870 | AGATAAATGCAAGCT[G/T]CATATATTTTCCAGA | 286053 |
rs537279805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113227 | TTGTGGTGGCTCACA[C/T]CTGTAATCCCAGTGC | 286053 |
rs537280050 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121166 | GTTGGAAAAGCTATA[C/T]ATACATGGTGAGAAG | 286053 |
rs537281883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205173 | CAAGTCCCTCCTTCT[A/G]CCTCAATGCAGAAAT | 286053 |
rs537303228 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277528 | TTTTTTTTTTTCGAG[A/G]TGAAGTCTCGCTTTG | 286053 |
rs537305077 | in-del | -/GAA | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140236 | GATACTAGCTTAAGT[-/GAA]GAAGAAGATTTGTAT | 286053 |
rs537316561 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216276 | GTGAGCATCAGTGTA[A/C]ATGTATCTGTTTGAG | 286053 |
rs537321866 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120051 | TATTTAAACAAATAT[A/G]TCTAAAATATTTTAA | 286053 |
rs537336586 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119302 | AAATAATTACTTGCT[C/G]TGTTCCCCTGTTTGC | 286053 |
rs537344471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249372 | CCCCACATCACAGCT[G/T]ACAGTCCATTTGGAG | 286053 |
rs537351025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211706 | CAACCCCATCAACAA[C/T]GTATGAGAGCCCATT | 286053 |
rs537375837 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303690 | CTCCACATACTCAAC[A/C]AAAATGGAGAGTAAA | 286053 |
rs537381627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163614 | ATGTTTTGACTACCC[C/G]CCTGCCCCACAAAAT | 286053 |
rs537382730 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245874 | CTACTAAAAATACAA[C/G]AACTAACTAGGTGTG | 286053 |
rs537382884 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353734 | CTAAAAATACAAAAA[G/T]TAGCTGGGCCTGGTG | 286053 |
rs537403895 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177023 | CTCTATTTTTTGCCC[A/T]AGTACTGGAATGGTT | 286053 |
rs537410380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363265 | CCCAGCACTTTGGGA[C/G]GCCAAGGCAGGTGGA | 286053 |
rs537411140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182644 | TGATTCTGGTTTTGC[C/T]TCTTTGGAGTAATAT | 286053 |
rs537442193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166773 | GGAAGACTGGTCTTC[C/G]TGGTTTAGAGTGCCT | 286053 |
rs537457606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099796 | TACAAATCTACAGAC[A/G]AGTTTTGCTCTAAGG | 286053 |
rs537466407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200578 | CCCTTTGTGGGTAAC[C/T]TGACTTTTCTCTCTG | 286053 |
rs537477563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215540 | AGCATGATTTATAGT[C/G]CTTTGGGTATATACC | 286053 |
rs537493952 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304997 | AGAGGGAGGGAGGGA[A/G]GGAAGGAAGGAAAGA | 286053 |
rs537517226 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172986 | ATATGGAGTTATTTC[C/T]ATCTTCCATTATCTT | 286053 |
rs537520860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165209 | GGCTGTGGCAAGGAT[C/T]AAATGAGATAACTTA | 286053 |
rs537529688 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146058 | TTAAGGAATTTGGAA[A/G]GAGCTTTCCAGAACC | 286053 |
rs537542973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265844 | TTCTCAGACTTGTAG[A/G]CCCCATTATTTGAGA | 286053 |
rs537551334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205806 | GTAAATACCAGTATC[A/G]TACTTAATAAAATAT | 286053 |
rs537555207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125130155 | CTTAGGTGTTTTGTA[A/G]AATGTCTCTCAGCTG | 286053 |
rs537558994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311939 | CAGGCATGGTGGCGC[A/G]TGCCTGTAATCCCAG | 286053 |
rs537562701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304495 | AGTTACAATGGTTTA[A/G]ACAAAGATGAGGGCC | 286053 |
rs537568568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296906 | AGAATAAAAAACAAC[A/T]GTGCTTATACTGATT | 286053 |
rs537575616 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325990 | TACCCGGGCGCGGTG[G/T]CTCATGCCTGTAATC | 286053 |
rs537589305 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114312 | CAGGGGTTTTTATCA[A/G]ATACCCTTACCCGCT | 286053 |
rs537594301 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148044 | GACGGCACTGCTTCC[A/G]GGTGTGCTGTGATCC | 286053 |
rs537603628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333759 | ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 286053 |
rs537630942 | snp | C/T | 0.110872 | 0.20771 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316773 | TCCTTCCTTCCTTCT[C/T]TCTCTCTCTTTCTTT | 286053 |
rs537659352 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218093 | ATTAGTGAAACCTAA[-/T]TTTTCTCCTTTTTAA | 286053 |
rs537686004 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212998 | GTTAAAAAAATCAAT[A/C/G]TGTAATAATATTTTC | 286053 |
rs537703859 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151024 | TTTTTTTTATTTTTT[A/T]TTTTTTTGAGGAGGT | 286053 |
rs537713670 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233283 | CCACTTAGAAGAAAA[G/T]AATTTTTAAAGCACG | 286053 |
rs537748041 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135833 | TAAATCTTGAAATAA[A/G]CTAGTGTTAGTCCTC | 286053 |
rs537752177 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252427 | AGCTACTCGGGAGGC[A/G]AGACAGGAGAATGGC | 286053 |
rs537760273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302523 | TTTACTTAGAGGTTA[A/T]TATGGGGTGAGAATT | 286053 |
rs537762985 | in-del | -/CAG | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138155 | TTAGATTGTAAAAGT[-/CAG]CAGCAGTACTAATAT | 286053 |
rs537769251 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238176 | ACAGTGAGAACTAAA[A/G]AAGATGGAAGACACA | 286053 |
rs537784185 | in-del | -/CTACTGCGAGCTGC | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173890 | GGGCAAGATGCTGAA[-/CTACTGCGAGCTGC]CTATTCCTCATATCT | 286053 |
rs537786256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277373 | GGCACAATGACTAAA[C/T]AATATGGTACTTTTC | 286053 |
rs537807584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355568 | AGCCAGGCATGGTGT[C/T]GTGCACCTATACTCC | 286053 |
rs537810750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319256 | TAACTGCATCCAAGA[A/G]CAAAACTCAAGAATG | 286053 |
rs537819374 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214561 | TGCTTAGAATTTTTT[A/T]AAATTAATAGACTTT | 286053 |
rs537836707 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342832 | GGCTCTGACCACTTT[C/G]TCAGGCCGTGGAGCT | 286053 |
rs537859165 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106697 | TCAAAAAAAAAAAAC[-/A]AAACAACTTTCATTT | 286053 |
rs537880526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207550 | AATTAGTATTGTGAC[A/G]CCATTTAAGTGTCCA | 286053 |
rs537901907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335393 | GTGCGTATGACAAAA[C/T]GCACTCAAGGTGATT | 286053 |
rs537918758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349256 | GAATTTCAAACTTGG[A/G]ATCAATGTGCTTTTG | 286053 |
rs537936311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196519 | CATCCATGTCCCTGC[A/G]GAGGACATGAACTCA | 286053 |
rs537939913 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205881 | TAAGATAATTATAAT[A/C]AATTGAATTTTAAAG | 286053 |
rs537977860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095441 | CTAAAAATTAAAAAA[A/G]AAAAATTGGCCAAGT | 286053 |
rs538010883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201868 | TTCAAGCTTCTCAGC[C/T]GCTTTGTTTACCTAC | 286053 |
rs538014135 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109111 | GGTAAAAAGGATTTG[A/T]TTTGTGTGCTATGTA | 286053 |
rs538024439 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253211 | ACACTTAAGGGAGCT[A/G]CCTGTTCCCTTCTCT | 286053 |
rs538025685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237614 | TAGAGTAATTCAGTT[A/G]TGCCCTATTCTGTTG | 286053 |
rs538026530 | in-del | -/AG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350643 | GATGCTGGCAGGCAA[-/AG]AGAGAGAGAGAGCTT | 286053 |
rs538027742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353074 | CTAGTGGTAGGCATT[A/G]CATTTGAGTTGTGCT | 286053 |
rs538043753 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107467 | AAAGTGCTGGGATTA[C/G]AGGCATGAGCCACCA | 286053 |
rs538048073 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290753 | TGCAAAGAGACAGTT[A/C]TCAGACAGGATGGGC | 286053 |
rs538050215 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152581 | TCTTGCTTTGACCCT[A/T]ACATTATGTGGCACT | 286053 |
rs538053047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180100 | GTCTGCTCTCAATTC[G/T]TCATGCTACAATTTT | 286053 |
rs538058604 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NSMCE2 | GRCh38.p7 | 8:125102145 | TGTGTTTGGTGGCCC[A/G]GGTGAGTGGCACAGT | 286053 |
rs538074096 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195703 | GCACTGACCATCAAC[A/C]CACTTTACAGTATTT | 286053 |
rs538087848 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349159 | CACAGGTGGGGTTAC[C/T]GGTAGCCCCAGCTAT | 286053 |
rs538092098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230866 | GCAGGGGGCAGCAGC[A/C]TGAGATACTAGTACA | 286053 |
rs538092197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221378 | AGACCTGAGTAGCTG[A/G]GATTACAGTTGTGTA | 286053 |
rs538094865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341634 | CTTCACAGTATCCTA[A/G]TGATACAGAGAAGAA | 286053 |
rs538112485 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133963 | CTCCAACCCCCAAGG[C/G]TTCAGATTCAGGCCT | 286053 |
rs538124774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194347 | AGGTAGAATTGTACA[C/G]TGTGTAGCCTTTTGA | 286053 |
rs538129017 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092916 | CAGGGTGAGGGCTGT[C/G]CTGTGTTTTGTAGGA | 286053 |
rs538141928 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343244 | GCACTAACAGATGTG[A/T]CAACTTATAACACAG | 286053 |
rs538149519 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146133 | AAGTGTTGTTTTATG[A/C]TAACAGATTGCCAAC | 286053 |
rs538153565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229629 | ATAAAATGACACCAA[A/G]CTTATGTTCTAGATG | 286053 |
rs538153751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208132 | CATCATTGACTGTAT[A/G]TGTGTGTGTGTTTCA | 286053 |
rs538170399 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093464 | GAGGCCAAGGCGGGC[A/G]GATCACTTGAGGTCG | 286053 |
rs538174919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160375 | AGTTTGGAGAGTAGA[G/T]TGGGCAGCAGGAAAC | 286053 |
rs538185998 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187814 | AAATTTTAAGTGTTA[A/C]TTTAATATGCAATAT | 286053 |
rs538192043 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289747 | AAGCTTAGGTTTTCT[G/T]TCTTGAGTAGGACCT | 286053 |
rs538200012 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344992 | TAAAAACAACAGTAA[C/T]TGAATGTCTGTCCCA | 286053 |
rs538218805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231927 | AGTATTCAGTATATG[C/T]TGGCATACTGAATAA | 286053 |
rs538222949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131024 | TTCAGTCAGAACACC[A/G]TTTCCAAGGTTACTT | 286053 |
rs538278869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239418 | TTTCGAGACTAGCCT[G/T]GCCAACATGATAAAG | 286053 |
rs538286074 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352032 | AATATATATACATAG[C/T]GGGGCTTAAATTTTC | 286053 |
rs538286814 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340831 | ACAAGGTCTTTCCAA[C/G]AATTAAAATTATCCT | 286053 |
rs538287850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344099 | GCCCCATCTTACCCA[A/T]ATTGAAATGTTGCAG | 286053 |
rs538305470 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109679 | TAGGGTGGTGATGTG[G/T]TTTATTTTGTTTCTT | 286053 |
rs538310764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161988 | TGCTGTTGGTACCAC[A/G]AAGCAAGTCCTCTCT | 286053 |
rs538319909 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272794 | ATATATATACACATG[C/T]GTATATATATACACA | 286053 |
rs538357201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248619 | GATCACACCACTGCA[C/T]TCCAGCCTGGGCGAC | 286053 |
rs538367596 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308379 | AAATCACAATTGGCA[A/G]TTATCCTCGCCTAAT | 286053 |
rs538400762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101540 | TAGCCCTCCCATCCC[C/T]TTAAAACTGTGAATT | 286053 |
rs538410483 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351085 | AGAAAAGGGAATAAC[C/G]AAGAATGATTCCAAA | 286053 |
rs538420808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116995 | TGGGTTCAAACAGTT[C/T]TCCTGCCTTAGCCTC | 286053 |
rs538436319 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263398 | AACTAGAAGGTTACT[A/T]CTAGCTTCATGTTAA | 286053 |
rs538438483 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291001 | CAGTAAATATTGGAT[C/G]AACAGAAACTAAGGT | 286053 |
rs538460571 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232115 | GCCTATAATCCCAGC[-/A]CTTTGGGAGGCTGAG | 286053 |
rs538460768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364804 | ACCTTGGGAAATAAG[A/G]GTTCTCTCCCCATTT | 286053 |
rs538460858 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169236 | TTCCTACCCGTTCTT[C/T]GATTTTCTTTCTCAC | 286053 |
rs538475448 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252399 | GGATGTGGTGGTGGG[C/T]GCCTGTAGTCCCAGC | 286053 |
rs538479708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117699 | TTTTTTATTATTTTT[A/G]GAGACAAGGTCTTGC | 286053 |
rs538480957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349785 | ACCACAAGACCATGT[C/G]TGGATTCTCCTTTGT | 286053 |
rs538483751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321183 | ACCATATCAGATACC[A/T]AGTGGAAACCTGGAT | 286053 |
rs538487715 | in-del | -/GCAACAGAGCGAGACTCCATCTCAAAAAAACAAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133707 | CGAGATCACGACTGG[lengthTooLong]GCAACAGAGCAAGAC | 286053 |
rs538490666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210208 | TGTTGTGGAGATTCA[A/G]TGAATTTATATATGA | 286053 |
rs538499413 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288758 | GCTAGGAGTTTTTTT[C/T]AGGACAAGTCTTTTC | 286053 |
rs538522437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351481 | CACCCTGGGCAGGGG[A/C]ATCTGGAGGTCAAGT | 286053 |
rs538529323 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108282 | GCAAGAACTTGTTAG[A/G]GGAGCAGTGTTAATG | 286053 |
rs538530447 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275173 | ACACCCCCCTTCCAT[A/G]TCCTTTTCCTGTCCA | 286053 |
rs538547953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151819 | CAGTTAAGGTGGGAA[C/G]ATAGCAACATCCTTT | 286053 |
rs538556133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291493 | AATCAAGTGCACAAT[A/G]GGAGATATACATTGG | 286053 |
rs538569144 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306712 | TTTATCTTGATATCC[A/T]GTCTTCATTTTGGTA | 286053 |
rs538574180 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284902 | ATAGCTAATGTGCTA[A/G]TTGCCTCAGAGATAA | 286053 |
rs538580089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336598 | TGATACTGCTGCAGA[A/G]TAGAAATGGGAGAAG | 286053 |
rs538583547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138501 | AAAGTGCTGGGATTA[A/C]AGATGTGAGCCACTG | 286053 |
rs538595917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197497 | AGGTTTATCAAAGAT[C/T]GGATGGTTGTAGATG | 286053 |
rs538600721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255201 | CAGGAGAGCTGCCCC[A/C]GTTAATGCTACATGA | 286053 |
rs538610633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155244 | GGGCAGGGAAGAATT[C/T]GGAGACTCCTTCTGG | 286053 |
rs538630830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293338 | TATTGTTATAACCAG[G/T]ACTGACGAAAATTTG | 286053 |
rs538631088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104365 | TAGGCTGATCCTTTC[C/T]AGGCTTATCGTTAAG | 286053 |
rs538659174 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198012 | TTGGTGTATAGGAAC[A/G]CTTGTGATTTTTGCA | 286053 |
rs538661542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190820 | AACAGCCGACATTGT[C/T]TGAGTGCTTACCTCT | 286053 |
rs538670560 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269096 | ACTTTGTTTTTTGTT[G/T]GTTTTTTTGAGACAG | 286053 |
rs538689256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204548 | CCCCGTACACAAAGT[A/G]TTAAGTTGACCATAC | 286053 |
rs538700640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294613 | ACTTTCTTATGCACG[G/T]AATAGAAACTGTCTC | 286053 |
rs538720982 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210568 | TTCAGCATCTGCACA[A/G]TGTTAGTCTCTTTCT | 286053 |
rs538735029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241197 | CGGATTTTGTATTTT[C/T]AGATTAAGGATACTG | 286053 |
rs538754643 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225046 | CTAAAGTCTGTGTTT[C/T]TAAAACAAAGTGCCT | 286053 |
rs538757074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286880 | AGAAAATCATATGTG[C/T]GTGGTGATTGTAATC | 286053 |
rs538769699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293937 | CAAAAAGAAATCCTG[A/T]ATAATCCTGTATCTG | 286053 |
rs538772184 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301742 | GTCTCGGCTCACTAC[A/G]ACCTCCGCTTACTGG | 286053 |
rs538785770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260542 | ACTTTCCTTCTCGGG[C/G]CCTGAGTTTCCTCAA | 286053 |
rs538796241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209190 | TATAAGGGAAATGCA[C/T]ATTTTGTTTTTATTG | 286053 |
rs538821897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133611 | TGAGGCATGGTGGCT[C/T]GCACCTGTAATCCCC | 286053 |
rs538832902 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357110 | CAGTCCTTACATGGG[A/G]GCCAACAGCAAATGC | 286053 |
rs538840835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234110 | AAGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCA | 286053 |
rs538850194 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273041 | TTGATGTATGTCAGC[C/T]GCCTATCATAGAACC | 286053 |
rs538851271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266912 | GGGAATATCACAGGA[C/G]AAAAACTTTATTTAT | 286053 |
rs538887946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125954 | CCAGATTTTTGTAAC[A/G]AGCAGTAAACTTCCC | 286053 |
rs538892055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134173 | TTATGTAAAAAATCT[A/G]TATTGATGAATGTTT | 286053 |
rs538894243 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228504 | GAATTTTGACCAGCA[C/G]AATCAAGGGAAGACT | 286053 |
rs538924540 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152161 | TAACTATAGTATTTG[-/A]ACTAACTTTAAGAAT | 286053 |
rs538924884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275200 | TCCATAGGAGAATGT[C/G]TTTCTCTCACTCCAT | 286053 |
rs538931595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268370 | TGGTCGTTTGAAGGA[A/G]AAAGAAGTTAAAAAA | 286053 |
rs538950155 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140465 | GTCAGGAGTTTGAGA[C/T]CAGCCTGGCCAACAT | 286053 |
rs538954495 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257755 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACTTCA | 286053 |
rs538955456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366267 | GCTCATAGGCTGGGC[A/G]CGGTGGCTCACGCCG | 286053 |
rs538967916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168346 | GGGAGGAGGATGGAA[A/G]AAAAGGAAGAAGACT | 286053 |
rs538991697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359915 | GTTACTCCAATAGCA[A/G]TGCAGAGATGGATTA | 286053 |
rs539004381 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224814 | GTTGAGCAATTTGCC[A/G]AACTTTATATTTACA | 286053 |
rs539004637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211838 | CTTTAGAATATTTCT[A/G]TCCCACCTCCCTTCA | 286053 |
rs539014315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184407 | TTTCCTCAGGCCACC[A/G]GTACACATTATTTGG | 286053 |
rs539028230 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221930 | GTGAAAGTCTTCACA[A/C]AGGGCCTAGCATAAA | 286053 |
rs539029110 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218410 | ATATTCTGAAAAATT[G/T]AGGGTTTTTTTTTTT | 286053 |
rs539073010 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111256 | GTCAGGGACATTTAC[C/T]GCCCTCATGAATAAC | 286053 |
rs539089499 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252578 | ATTTATATTTTCTTG[C/T]ATTTGACTATCTCAA | 286053 |
rs539093599 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177739 | CCCCAAAGGACAAGC[A/C/G]CTTCTCTAATGGAAA | 286053 |
rs539102202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351374 | AAAAAAAACATATTC[A/G]AGTTACCTAACTCTA | 286053 |
rs539103059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220419 | AATGGTTTGTATAGA[A/G]AGAGTTTTCCTGTGA | 286053 |
rs539107099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317138 | CAGAATACCCTCAAG[A/T]TGAGTCCATCCTGGG | 286053 |
rs539111554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353566 | CCCACAGCAAACATA[C/G]TATAATATGGTACCT | 286053 |
rs539120281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263273 | GCCATTTCCCAGGGA[A/T]CTATGTAGGTATGTC | 286053 |
rs539123430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118734 | GAGAACTATACGACT[A/G]TTAAGGTTAAATTTT | 286053 |
rs539134331 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091921 | TCTAGGCAGGGGAAA[C/T]TGGGGTGCCACCAGA | 286053 |
rs539134712 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122058 | CAGTGTAGATAGCTC[G/T]TTTGCAGAGCTCTGA | 286053 |
rs539148811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360774 | AGTATTTCTGGGTTC[A/G]CTTTGTTTAGAAATG | 286053 |
rs539171016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316811 | TCTTCTTTCCTCTTG[C/T]TCTGTTGCCAGGCTG | 286053 |
rs539175339 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124683 | AGGTCTTGCTATGTT[A/G]GATTGGCTGGTCATG | 286053 |
rs539183542 | snp | G/T | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090904 | GTTCTGAAATGAGGC[G/T]GAACCTGAAATCCTG | 286053 |
rs539187123 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092596 | GGGAAAAGCAATTGT[A/G]TGAGAAGGATTCAGA | 286053 |
rs539206898 | snp | A/C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334427 | AGGGGATCCATGAAC[A/C/G]TTGAATTCAGAGAGC | 286053 |
rs539210836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330686 | CTCGAATGTACGCTA[G/T]GTACTAAAGGAAACA | 286053 |
rs539213088 | snp | A/G | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362513 | CAGGGACTGGTGCAC[A/G]GCAGGACCTGAAGTG | 286053 |
rs539234063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185059 | CACTAACTTTATTAT[A/G]TAAGAACATAAATAC | 286053 |
rs539268532 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359662 | TTAGTTTCCTTATCC[A/G]TAAATGAATGACAAT | 286053 |
rs539275580 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102629 | TTTTATTCTACACAC[C/T]GCAGCAGGGTACTGA | 286053 |
rs539306021 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330858 | AGTGTGGGGTTTGGA[C/T]TAGGTGACCACAGCT | 286053 |
rs539307176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164472 | ATTTATGATTTTGTA[C/T]ATCTCTTATTGTAAA | 286053 |
rs539322205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282410 | TGAGCCACTGCACCC[A/G]GCAAGATCCCTTAAT | 286053 |
rs539322822 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218014 | TTGTTACTGTCATAT[G/T]AGCCTCCTGATAATT | 286053 |
rs539330098 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105219 | ACAGTTATTCATTTA[C/T]GGCTAACAGCAGGTG | 286053 |
rs539339198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234764 | AATCATCTCTCTCAA[C/T]GTAAACTTGGAGCTA | 286053 |
rs539340634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323291 | TTTTTTTGTAGATAT[C/T]GACGAGATTATTCTG | 286053 |
rs539357734 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293943 | GAAATCCTGTATAAT[A/C]CTGTATCTGTTAGCA | 286053 |
rs539364875 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314685 | CACACCTCTGGAAGT[A/G]GAGCTGTGATCCTGC | 286053 |
rs539368254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148616 | GCAGAATTTTGGAAA[A/C]GCAGTTTATACTGTT | 286053 |
rs539405019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333334 | GCCACCATGCCTGGG[C/T]AATTTTTTATTTTTT | 286053 |
rs539409054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201148 | GAAGTTTGTTATTAC[C/T]GACCTTCTGAAGCCT | 286053 |
rs539410256 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306572 | TTTTTTCCTGAACAC[A/G]TAATTGCTCTAGGAG | 286053 |
rs539412562 | in-del | -/AA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323368 | TGGAAAAAAAAGGAC[-/AA]AGTTAGAGAACTTAT | 286053 |
rs539429537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151629 | CATACAATTGAGACC[A/G]GGTTTAGTTACTCAT | 286053 |
rs539430621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179278 | GGAAGTTAAAGGCTA[C/T]AGTAAACTGTGATCA | 286053 |
rs539430630 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119644 | TAAGCAAAGATGACA[C/G]CTTATGGAAGAAGTA | 286053 |
rs539442065 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294983 | TGAACTTTTTCTCCT[A/C]TGTGATCCATCAGTC | 286053 |
rs539450010 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101354 | GGAAGGGCAGAAGGG[A/T]AGGCTCTAATGCTAA | 286053 |
rs539485587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244045 | AGTTTTTTTTTTAAG[C/T]AGCATAGAATTAATT | 286053 |
rs539492562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144363 | GTCTGTTAGCCATGC[C/T]CACCTGGATTTGGGA | 286053 |
rs539523060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270588 | TATATCCTGGGTAGG[A/G]TAAAAGATAGGCCTA | 286053 |
rs539537937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228662 | TCATATTTGAGAAAA[A/G]TGAATGTCCCAGAGA | 286053 |
rs539542465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142688 | TGGCTCACCACAACC[A/T]CCACCTCCCAGGTTC | 286053 |
rs539551749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245788 | CATGTAATCCCAGCA[C/T]TTTGGGAGGCCCAGG | 286053 |
rs539565823 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367613 | TTGGGAGGCATTTTC[C/T]ATGAGTATAGTAAAT | 286053 |
rs539571952 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274382 | CTGTCACCTCAGTGA[-/T]TTTTTTTTAGTTCAT | 286053 |
rs539578282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199294 | CGATTTTAGATCTTT[C/T]CTGCTTTCTCTTATG | 286053 |
rs539590123 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285231 | GTCCATTCCCACTTG[C/T]CAGATGGAGAGAAAG | 286053 |
rs539598229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121806 | GTAGGTATCATTACC[A/G]TTATACATATGAGTA | 286053 |
rs539598624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149221 | TTGAGATATTTGTGT[A/G]TTCTTTGCTGCCTGG | 286053 |
rs539603500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257725 | ATTTTTAGTAGAAAC[A/G]GGGTTTCATTGTGTT | 286053 |
rs539613235 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213544 | CCTCTCCTCTCCCCT[C/G]CACTCCCCTCCCCCT | 286053 |
rs539618306 | snp | A/T | 0.183568 | 0.241012 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250335 | ATGTTTTTCTTTTTA[A/T]AAAAAAAGCATCCTT | 286053 |
rs539634472 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274886 | AGTGAGCCAAGATCG[C/T]GCCATTGCACTCCAG | 286053 |
rs539635912 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252941 | TACTCCCTTAAGCCT[A/T]AATTTTCTTACCTAT | 286053 |
rs539639596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221113 | AAGGCATATAAATGA[A/G]TTTTTCATATGGCTT | 286053 |
rs539642240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303202 | CCCTCTGTGAACCTG[C/T]AGTTCAGCTTTGACT | 286053 |
rs539650602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354350 | TATCTTACCATACTG[A/G]GAAATTTTTATGAAG | 286053 |
rs539656349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257019 | TTAGTTAAAGGAGTC[C/T]GGGCCTGTAATCGCA | 286053 |
rs539667583 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125362009 | TGGGACCCCAAGACC[C/T]GGTTCCCTTTGCTCA | 286053 |
rs539687240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142272 | CTGTTATTGTACCCA[C/T]TATATATAAAAGGAA | 286053 |
rs539711173 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243123 | AAAAAGACATTGGCT[C/T]ACCCCTGAAAATGTA | 286053 |
rs539714556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204957 | GCAAGAGTCAAGTAG[G/T]GCATGGGCTTTCCAT | 286053 |
rs539723888 | in-del | -/AC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276383 | TCTTCCCACCCTAAA[-/AC]CCCTCTTCCTTACTC | 286053 |
rs539726109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348334 | TTCTAGTATTTTTGT[G/T]GAAATTTATGTTTGT | 286053 |
rs539732940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339741 | CTGTGCCTCCAGTCA[A/T]TTTAAGAAGTCCTTG | 286053 |
rs539735026 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328840 | TCACAGCTAGAAATA[A/C]TATCCAAGGTCATTA | 286053 |
rs539737198 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156992 | AATTTCTCCCTTAGA[A/C]AGCTAATAATTTATT | 286053 |
rs539744389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112816 | GAAAGAGTTCAAGAG[A/G]TCTATTGTATAATAT | 286053 |
rs539746599 | snp | A/G | | | missense | NSMCE2 | GRCh38.p7 | 8:125182248 | AGCTGAAAGAACTAA[A/G]GAAGCAATGTAAGTC | 286053 |
rs539748873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213087 | ATAAAATGAGAATAG[A/G]GAAAAAGAAAAAAAG | 286053 |
rs539769518 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152584 | TGCTTTGACCCTTAC[A/G]TTATGTGGCACTTAC | 286053 |
rs539797835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143885 | AGAAGTTTTGTAGAC[C/T]CATAAGGTATGAAGT | 286053 |
rs539810682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194718 | TATTTATAAAATTTT[A/T]AAAAAAAGAAATGGA | 286053 |
rs539836235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151975 | GTCTTGTATTTCTGG[C/T]TTCGTTATTTGCCTT | 286053 |
rs539836377 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295895 | GCATATCATGACCCA[A/G]TAATAACCGTTGCCC | 286053 |
rs539837548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290266 | ATGTCTTAGTCAAAA[C/T]GTGACTGAAAGGAAA | 286053 |
rs539846966 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298033 | TGGGAGGCTTAGGCA[G/T]GTGGACCACCTGAGA | 286053 |
rs539851775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251710 | TCATAATTAGCTGAC[A/T]TCATCTTTACCACCT | 286053 |
rs539869216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258966 | GTAGTGCAATGGCAC[A/G]ATCTCGGCTCACTGC | 286053 |
rs539895331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158532 | AGGTAGGTACTGAGG[C/T]GCCCAGTGTGATTAT | 286053 |
rs539912122 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136879 | AATGTCAATATAAGT[A/G]AGGAAAAAATAAAAA | 286053 |
rs539936095 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333795 | TGGGATTACAGGCGT[A/G]AGCCACCGCGCCCGG | 286053 |
rs539960225 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100824 | CTTCAGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 286053 |
rs539965185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159659 | TTAGGCATCTACTGG[C/G]GGTTTTGGAATGTAT | 286053 |
rs539986812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355071 | CCAAGATATTTCATC[A/G]TGCTTATGCAAATAT | 286053 |
rs540018947 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286503 | TTTTTAGTAGAGATG[C/G]GGTGTTGCCATGTTG | 286053 |
rs540020794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122254 | TATGAAGATACTTCA[A/G]CAAATCTCTAGATCC | 286053 |
rs540021680 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310595 | GTTACTTTAAGCCCC[C/T]TTTTTTTTTGTCTTC | 286053 |
rs540025641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361708 | TTGGGAGCGAAGAGC[A/G]CTAAACAAATAGCTG | 286053 |
rs540025833 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245721 | GGATTACTGAAAATT[G/T]AAACAAAATTAAGAT | 286053 |
rs540028185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158089 | TCTTCAGAACCCACT[C/T]TGGGAAGTGCTGCTG | 286053 |
rs540036349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166021 | CATAATCTTTATTGT[A/G]TTGGGTGAGATGTGA | 286053 |
rs540039943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221466 | CCAGGCTGGTCTTGA[A/G]CTCCTGGGCTCAAGC | 286053 |
rs540042484 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212421 | CCTCCTAGAGCTGAG[G/T]CAGTGAGAGCCCGGT | 286053 |
rs540047834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321452 | CGTGGTGAATTCTAC[C/G]AAGTATTTAAGGAAA | 286053 |
rs540059167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271111 | CTAAAAAACACAAAA[C/T]TTTGCCAGGCATGGT | 286053 |
rs540078687 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314964 | GTGGGGATCAAGGAG[A/G]ACCTCAGAGATGTAA | 286053 |
rs540097058 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272759 | TATATACACACGTAT[A/G]TATATATACACACAC | 286053 |
rs540098639 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113745 | TCAGCAGGATCCACC[A/G]TGTTCACATAGATGA | 286053 |
rs540109868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297018 | TCTTTCTCATTGCAA[A/G]CATTAAGTTATTCTT | 286053 |
rs540120317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257979 | AGAGATGGAAAATAC[A/G]TAAATACTTTTATGA | 286053 |
rs540133265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180221 | TTATATTGCCTTTCT[A/G]TCTTCTCTTTTCCAA | 286053 |
rs540133616 | in-del | -/GGA | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201236 | GAGCTGTGATCCGTT[-/GGA]GGAGAAGAGGCACTT | 286053 |
rs540141908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129665 | TACATGCAAGTTAAA[A/G]ATTGTTTATACTAAA | 286053 |
rs540149655 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230835 | TTCAAGATTTTGCCC[-/CT]GTCTTTCTTAGACAG | 286053 |
rs540172281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165409 | GGTATTTTCCAATGA[A/G]TGGTGCCTTCTTCAG | 286053 |
rs540173979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165898 | TCAGGGAGCCATATT[A/T]ATTATAGAGAAAGCA | 286053 |
rs540188607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108425 | GCTGATACTAAGGCA[A/G]CCAGTATCAGCACTT | 286053 |
rs540194978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245435 | ACAAGTCAAAGGCTA[C/T]GTCAAAACTATAGTT | 286053 |
rs540200793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341744 | CCGAAGTCCATTCTT[A/G]TATGAAACTACAGAA | 286053 |
rs540205322 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150999 | CATATGGTGAGGAGG[-/T]TTTTTTTTATTTTTT | 286053 |
rs540211216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216358 | TCAAATGATCTGTGG[G/T]TCCGGGCGCGATGGC | 286053 |
rs540230156 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224014 | GCTAATTTTTTTAAA[-/T]TTTTAGTAGAGAGGA | 286053 |
rs540230988 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116606 | TGCACACATGGGAGT[A/G]TCTGTGTTTTGAAAG | 286053 |
rs540234261 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093715 | GCGACAGAGCGAAAC[G/T]CTGTCTCAAAAAATA | 286053 |
rs540244484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252102 | AGCTGAGATTGCCCA[A/G]GAGAGTATAGTCAGC | 286053 |
rs540260355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110055 | AGTAGTTTTAGTAAG[C/T]GCTTTAGGTTTAGTT | 286053 |
rs540271872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209263 | ACAAATAATGTGTAT[C/G]TCTGCTGACGAAGAA | 286053 |
rs540274205 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312406 | TGAGGCGAGTGGATC[A/G]CAAGGTCAGGAGTTC | 286053 |
rs540317212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223343 | AGCCTGGGCAACAGA[A/G]CAAGACCCTGTCCCA | 286053 |
rs540325425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299654 | ATTAAGCACCCCTAA[A/G]GAAAATGTAACAACC | 286053 |
rs540327884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246106 | ACATATTTGAAAAGT[A/G]ATATTTTTAACTCTG | 286053 |
rs540335792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207664 | TAACCATTTATTTGG[C/T]TCGTGACTATTTGGC | 286053 |
rs540337307 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359962 | AAAAAAGTCAGTTAG[A/G]ATGCTTTTACAGTGG | 286053 |
rs540343190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215888 | AGGAGTTCAACACCA[A/G]CTTGGGCAACATAAC | 286053 |
rs540347424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174468 | TAAATAAATCATTCC[A/G]GTTGGTCATCGTATT | 286053 |
rs540370792 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360647 | GGTTCTGAAGGCCAG[G/T]TGCATTTGGGCAGCA | 286053 |
rs540370871 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137392 | TTCTGTTTTAAAGGA[G/T]GCTGACCCTATTCGT | 286053 |
rs540374715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123876 | ATTAGCTTTTTTATT[C/T]TTTTATTTGGTGACA | 286053 |
rs540390902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306240 | GAGGCTGAGGCGAGA[G/T]GATGGCTTGAGCCCA | 286053 |
rs540398614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318707 | CTGTGAAACAACCAC[A/G]GCACTCAAGGCATTG | 286053 |
rs540406119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214189 | TAAATACCAGGTTGG[C/T]AGGCAAAATTAGGGA | 286053 |
rs540411892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310996 | ATCTCACTTTTAATA[C/T]GTTAGATAATTACTC | 286053 |
rs540426885 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327923 | AATCTGGGAACTCCC[G/T]TTGAACCTTTTGAGG | 286053 |
rs540444498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125362066 | CTGCAGCGAAATGCT[C/T]TGCCCGGGTAGTGCC | 286053 |
rs540462198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115220 | ATGGAAATGGGCAAA[C/T]GTCACAAATTAGACC | 286053 |
rs540494474 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162488 | AAATTTAATTAATGA[-/T]TTTTTTTTTTCTGTG | 286053 |
rs540495948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172536 | CCCCTCCCCAAAAGG[A/G]GGAATGATACATCTT | 286053 |
rs540512473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258496 | GCTCCCCTGAGTGAG[A/G]GAGAATGGGCAAGCC | 286053 |
rs540512998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334734 | GGCAGACTATGTGTA[C/T]GAAGGATTGGGCCAA | 286053 |
rs540513622 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188621 | GTAACCTTTGCCTTT[A/T]CTTTCTCATAATATA | 286053 |
rs540516506 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167437 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCATGAGG | 286053 |
rs540526528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121616 | TGAATGTATTTTTAC[A/G]TTTTATGACCTAGCA | 286053 |
rs540532191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319449 | GGCATTAAAACAATT[A/T]TTGTGATTGCATTCC | 286053 |
rs540553661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272400 | TTTTTCACTTACTTA[C/T]TCAAAAATCTCAGCA | 286053 |
rs540555186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355201 | GGTGATGGCCCACAG[C/T]CATCAGTTCTATGGA | 286053 |
rs540555740 | snp | A/T | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128485 | ATACTCAAATTTCTG[A/T]CATACGCATCTATGT | 286053 |
rs540555779 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153769 | AGATAATGTATATCA[A/G]AATGCTTTGGCATTC | 286053 |
rs540568126 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094314 | TATATCAAAGAAGGT[A/G]CTGTTAGAGTCAGAG | 286053 |
rs540581944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232031 | CACCCACTGTATCTC[A/G]CAGTATCATCTTGAA | 286053 |
rs540587110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266953 | AATCTGAACATTTGG[A/T]TTGAGCATCAGGCAC | 286053 |
rs540596999 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333267 | TTTGACCTCCTGGGC[A/C]CAAGTAATCCTCCCC | 286053 |
rs540603337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305454 | GGAGTAGGGACAAGA[A/G]GCTGAAGAGAAGTCT | 286053 |
rs540603480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132876 | TAAAAGTACAGTAAC[A/G]TAGAACATGAGATAA | 286053 |
rs540612746 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309197 | AGGTTGCAATGAGCC[A/G]AGATCACGCCATTCA | 286053 |
rs540616452 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278911 | TCAAACCGAGAACCA[C/G]GATGGGATTGGAATT | 286053 |
rs540634117 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289844 | ACACTAGCTGATCAA[C/T]TACTGGTCTTAAATC | 286053 |
rs540642851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160631 | TGTCTATAACAATGA[A/G]AAAGATACCGCACCC | 286053 |
rs540647240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266411 | AATTCCTACAGACTT[C/T]ACTCTTTAGTGAAGT | 286053 |
rs540648433 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239960 | CCCTGCCCCTTCTTG[C/T]TCATTGCTGAGGCCA | 286053 |
rs540679713 | in-del | -/AAAAAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327281 | AAAAAAAAAAAAAAA[-/AAAAAA]GAGAGAGAAACCAAA | 286053 |
rs540681334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280553 | ACAGTGAGAAAAACT[A/G]CATATTCACTATCAT | 286053 |
rs540686587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365618 | CCCAGCACTTTGGGA[A/G]GCCGAGGCAGGTGGA | 286053 |
rs540690889 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117855 | CCATATATAAATGCG[G/T]TAGTAACTGGCTTTC | 286053 |
rs540703078 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267732 | CAGTGAGCCAAGATC[A/G]TGCCACTGCATTCTA | 286053 |
rs540741207 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299041 | ATAGTTGATGCTAGT[A/G]AAAAATAATGTTCTG | 286053 |
rs540748282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132075 | AGCAACTAAAAATAT[A/G]TGTGTATTCATATTC | 286053 |
rs540753650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350557 | AGGTTTAATGGACTT[A/G]ACGTTCCACATGGCT | 286053 |
rs540775141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365134 | GTGGCCCACTCAGTC[G/T]CTCTTCTAGGAGGGC | 286053 |
rs540794420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158577 | TCAGTGGCACCAGGC[C/T]ATCCTAGCAGCTAAT | 286053 |
rs540802044 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239513 | ACTCGGGTGGTTGAG[A/T]CATGAGAATTGCTTT | 286053 |
rs540808314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130602 | CCAAGATCTGGGCTC[C/T]AGATGTGCTTGCTGC | 286053 |
rs540829150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278307 | CCTTGAATGGCACCA[A/G]TAAGGCCCTTCAGAG | 286053 |
rs540835535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247554 | ACACGGTGAAACCCC[A/G]TCTCCACTGAAAATA | 286053 |
rs540837213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173917 | GCCTATTCCTCATAT[C/T]TGTGAAATTGGGATA | 286053 |
rs540843664 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137373 | AACTGTTCCTTCATT[A/G]ACTTTCTGTTTTAAA | 286053 |
rs540864058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327004 | GAGGTGGCTCACACC[C/T]GTAATCCCAGCACTT | 286053 |
rs540871370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131143 | ATTACAGGATCCCCT[C/G]ATTCCTGATTGTTGG | 286053 |
rs540875905 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256275 | GGACAGAGTGAGACT[A/C]CGTCTCAAAAAAAAA | 286053 |
rs540876619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096121 | TTCTCTATCATCAGC[A/G]TATAGCTTTACTAAG | 286053 |
rs540891672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363681 | GGGCGGGGAGGGAGG[A/G]AAGGAAGGAAGGCAG | 286053 |
rs540896949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253984 | GTTCAGGATGCTTCT[C/T]AAAAGGCCTAGAAGA | 286053 |
rs540909705 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336678 | GTGTGGCATTTTACT[A/T]CCTGGTATATGGAAG | 286053 |
rs540919785 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110808 | AATGTTATCTGATTT[A/T]TTTTTTTAAATACCC | 286053 |
rs540930167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240485 | ATAATGAAGCCAATC[G/T]TTCACATACTGGCAG | 286053 |
rs540939628 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281695 | TCTTACCCGCCTCAG[A/C]CTCCCAAAGTGCTGG | 286053 |
rs540945274 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311762 | CTAAATGGTGAAATA[C/G]AATCAAGAAATGATA | 286053 |
rs540963777 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272107 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 286053 |
rs540968539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202320 | CTGGGAGCTGCAGAC[C/T]GGAGCTGTTCCTATT | 286053 |
rs540995170 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253644 | TAAATCTTCATCTTG[C/G/T]TTTGTATTGTAAAGG | 286053 |
rs541024326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287936 | CATTACTCCCTTGTG[C/T]GGGATCCTTCTCAAC | 286053 |
rs541066441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140890 | TTAAATTCACAGTTT[A/C]TTTTCAGTCTACCAG | 286053 |
rs541075089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090945 | GTGAAGGACAATTAG[A/G]GAAGGTGTCCCTTGT | 286053 |
rs541082431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147014 | CTACAGCTATTATAT[A/G]TACATATATAATCAT | 286053 |
rs541086377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254469 | AGTTTAATTAGCTTT[A/G]ACTTGCTAAAAGAAA | 286053 |
rs541089904 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213193 | TTAAGCTTTTATTCT[C/T]TGTTGTGAGATTTTC | 286053 |
rs541091492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245981 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 286053 |
rs541099944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155560 | AGTAATGCAAGTCAT[A/G]GCAGTAGTTGATTTA | 286053 |
rs541104963 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274649 | AAGTAACTATTTGTG[A/G]CCAGGCACGGTGGCT | 286053 |
rs541114836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190901 | TTGAGATGGAGTTTC[A/G]CTCTTATTGCCCAGG | 286053 |
rs541117137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096583 | TCACTTTTTGTTTTG[A/G]TTGTGAGGAAGCTCA | 286053 |
rs541120598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182996 | TTTTTTCACATTAGC[A/T]TCTATTTAGTCCTGT | 286053 |
rs541126755 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192912 | GTATCATTCTAATAT[A/G]TTTTCTTTGGAATTC | 286053 |
rs541127589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322684 | TAAAATTTGCAGATA[A/G]CATGATCATCTGTGC | 286053 |
rs541135204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314078 | TAGCAAACGTGCAGA[A/G]ATGTGAATTGAATGA | 286053 |
rs541143692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140058 | CTGTCCCAAGAACCT[C/T]ACAGCAATGGTTGCC | 286053 |
rs541154728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153571 | CAGCTTGGGAGGGGC[C/T]GGGATAATATACTTG | 286053 |
rs541165124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288516 | AATTCCTTTTACCAG[A/G]GATATTTCTCAAATC | 286053 |
rs541180050 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120194 | ACATGTGAAAAGTGG[C/G]TACTGTATTAGATAA | 286053 |
rs541200115 | in-del | -/AAAAT | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223063 | TGAGACCCTGTCTCA[-/AAAAT]AAAATAAAATAAAAT | 286053 |
rs541207633 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298683 | ATATCAAATTCATCT[G/T]TGGGTTTTTTTTTGT | 286053 |
rs541227863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163133 | ACACTTTGGGAGGCC[A/G]AGGTGGGAGGATCGC | 286053 |
rs541234374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111570 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACTTGA | 286053 |
rs541246975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197562 | ATTGGTCTGTATATC[C/T]GTTTTGGTACCAGTA | 286053 |
rs541251402 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358547 | CCTTCCCCTTCTTCC[A/T]TGACCACGGAGGACC | 286053 |
rs541257907 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189936 | AATTGATGAAGTTTG[C/T]TGGCTCTTCTATGGT | 286053 |
rs541265465 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326938 | TCCAGCCTGGGTGAC[A/C]TGAGCAAAACTCCAT | 286053 |
rs541281766 | in-del | -/ATA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275000 | GACAATCTGAAGATG[-/ATA]ATAATAATAATAATA | 286053 |
rs541292517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279904 | GAATGACTTAGTAAC[C/T]CCAGCGCAGTCATCT | 286053 |
rs541300227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328979 | CCTGTCCCATCAGAC[A/T]GTCTGCAGACCAAGG | 286053 |
rs541305514 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355097 | AATATTTCAAAGTCC[A/G]AAATCCGAAACACTT | 286053 |
rs541307646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161524 | CAGTAAAGGCTGGGT[A/G]TGGTGGCTCACACCT | 286053 |
rs541320894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248088 | ACTATATGTTAAATC[G/T]AAAATTTATACTTTA | 286053 |
rs541323711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294269 | TGCTGCTGTGAACAT[C/T]TGTGTACAGTGGACA | 286053 |
rs541329956 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188304 | TGGTTTTTATGTTTT[C/G]CTTACTGCTGTATTC | 286053 |
rs541340172 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169389 | CTTAATGATAGATTT[C/G]ACATTCTCTACTTAA | 286053 |
rs541364829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118120 | TTTAGGAGGCCGAGG[C/T]GGGCGGATCACCTGA | 286053 |
rs541371904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162635 | AAATGAGATAACATT[A/G]TGTGAAAGTACTTGG | 286053 |
rs541373448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286448 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCGCCCAC | 286053 |
rs541377673 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111663 | AAATTAGCTGGGTGT[A/G]GTGGTGTGTGCCTAT | 286053 |
rs541378399 | in-del | -/ATT | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185800 | AAACATAAAGGAAAA[-/ATT]ATTGAGAAGAGTGGC | 286053 |
rs541381112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301337 | GTTTCCCTGGCCAAA[G/T]GTAATAGAATGCAGT | 286053 |
rs541384369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249540 | TTCTCTATTTACTCC[A/G]AAACAAATGAGTGGA | 286053 |
rs541388590 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123659 | CATGTCCCATGCCAG[C/T]CCTATTTGCCGTTAT | 286053 |
rs541393190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352334 | AATACAAAATTAGCC[A/G]AGGTGGTGGTGCATG | 286053 |
rs541398564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205470 | TCCATCAGTAAAATG[G/T]TCTGTATCTGCTGCT | 286053 |
rs541401742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242349 | GCTGAAGGGCATATT[C/G]GATGGGCTCCTGGTT | 286053 |
rs541402627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302694 | CCGAGAAAGGACCCT[A/G]AGACAGAGGGGTTGG | 286053 |
rs541406024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097882 | GAAAGCTTTGGATAC[C/T]GTGCTAATTATGTTG | 286053 |
rs541415373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148746 | ACAAAACAATACTTT[C/T]CTTTAACTAGGTAAG | 286053 |
rs541423127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346350 | AGATAAAGATGGAGA[A/G]TGGACAGGCTATACG | 286053 |
rs541436068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213149 | CTGTATGAAAAAGAA[A/G]TGTTGAACATTTGTA | 286053 |
rs541437375 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114760 | TGATACACACACTAA[C/T]GTATGCATACATACA | 286053 |
rs541439683 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149458 | AGATATATGAATGGA[A/G]AGTCTTTGAGTAGGT | 286053 |
rs541445004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098472 | TCTTACGTACATTTT[C/T]AAAGGTTTACTCTGG | 286053 |
rs541445027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337752 | ATACAAAAATTAGCC[G/T]GGCGTGGTGGCACAT | 286053 |
rs541464638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165579 | CTATTTGCAGACTTG[A/G]CCACACTGTAGTCTC | 286053 |
rs541465898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309598 | GGCGTGGTGGCACAT[A/G]CTTGCAGTCCCAGCT | 286053 |
rs541485254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353879 | CAAGGGCAAGACTCC[A/G]TCTCAAAAACTAAAA | 286053 |
rs541520334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104772 | CCGAGCATGGTGGCT[C/T]CTACCTGTAATCCCA | 286053 |
rs541522699 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117831 | TTTAATGCCTATTAG[A/G]TGTTGAATCCATATA | 286053 |
rs541538667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204619 | TAGTAGCTTGTTTAT[A/G]TACATTTTCCTCCTG | 286053 |
rs541575138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295884 | ATGAAACTGAAGCAT[A/G]TCATGACCCAATAAT | 286053 |
rs541580031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186072 | GCCTGCCTCCTGATT[A/T]TCTATGGCCTGCAAG | 286053 |
rs541580283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178156 | ATCATTTTTTTTAAA[C/T]TCTCATTATCACTTT | 286053 |
rs541582548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118856 | GATTGATGCAGATCC[G/T]TTCACAAAATAAAAA | 286053 |
rs541592527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315995 | GTTTTTTAGCAGAGA[C/T]GAGCTCTCACTGTGT | 286053 |
rs541592992 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170356 | ATATCCAGTCCATCA[A/G]TAAACCTTACTCTTT | 286053 |
rs541605295 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308412 | TCTTCTTGAGTCAGA[G/T]AAGTCTTTTTCCTTT | 286053 |
rs541624115 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174756 | AGTAGTGTATTACAA[C/T]ACCTTGGCAAACCGT | 286053 |
rs541634973 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227408 | GAGCAAGTCATGCCA[A/G]CCAGGGCCTTCCCCT | 286053 |
rs541639713 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178784 | CTGAGGCAGGAGAAT[C/G]GTGTGAACCCGGGAG | 286053 |
rs541668708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301824 | CCAACCAACCATGCC[C/T]GGCTAATTTTTGTAG | 286053 |
rs541676049 | in-del | -/G | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091569 | CAGCGGGGAGGGGAA[-/G]GGGGGCCATGCAAAA | 286053 |
rs541688935 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323679 | ATATGTAAAAATTAA[C/T]TCAAAGTGGATCATA | 286053 |
rs541712370 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213034 | CAAAAATTATATTGA[A/G]CAGTAAATGATGATT | 286053 |
rs541712543 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352507 | AAATTTGGGAGCAGA[A/G]GAGCTCCCAGAACCA | 286053 |
rs541714199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185449 | GTAGCTGGGATTATA[C/T]GTGCATGCCACCAAA | 286053 |
rs541739812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345413 | ACTATTTTCATCTTT[C/T]TATTGTGGTAAATTT | 286053 |
rs541762425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112298 | GTGTATTGTTGGTGC[A/G]AATGTAAATCAGTAC | 286053 |
rs541796971 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257444 | TCCTGTGTCAAATGT[A/G]AACAGTCAGTCCAGT | 286053 |
rs541799810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230107 | TTTTGAAAACCTTGC[A/G]GATTGTATGTAGTTC | 286053 |
rs541804091 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125129844 | TTTACCAAAGTTGTA[C/G]ATAGTGGAGTTCCCA | 286053 |
rs541856099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157688 | AGGTTTCGAAGTAAC[A/G]TAGCTGCTAATAGGT | 286053 |
rs541859497 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229127 | TGATGAGTCAGAAAA[A/C]AATGTTGCAGGAAGC | 286053 |
rs541865425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122328 | GATCATCTTTGTTTG[A/G]TTGTTTCTCTAGCCA | 286053 |
rs541866326 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360968 | TATTGTTGAGACTTT[A/T]GCCCCAGCCAAGCAC | 286053 |
rs541877790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362706 | ATTCTTGAGCCTGCA[A/G]TTCTGTCAGTAGGCC | 286053 |
rs541886044 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354872 | ATCCAAAACCCACAA[C/T]GCTCCAAAATCCAAA | 286053 |
rs541934565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271918 | TGGGGATTATTGCTC[C/T]GTTTTTCAGGTGGGA | 286053 |
rs541938104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257751 | GTGTTAGCCAGGATG[A/G]TCTCGATCTCCTGAC | 286053 |
rs541949652 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164762 | TAAAAATGAAATAAA[C/T]TTTTTTCTAGTTTTA | 286053 |
rs541952665 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093593 | TGGTGTGTCCTGGCA[C/T]ACACCTGTAATCCCA | 286053 |
rs541965702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362144 | CTGCACAGCGATGAT[G/T]CGGCAGCTGAAGATC | 286053 |
rs541983187 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136845 | TCAGTCAATTAAATT[C/G]AAAATAAAACATCTT | 286053 |
rs541990213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332907 | TAAGCTACCCTGCAA[C/T]GTGCTTGGAAATCAT | 286053 |
rs542023679 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236160 | AACTGAAACTTTTTG[C/T]GCTTAACGTAGAATT | 286053 |
rs542030152 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298575 | TTAAACCATCTCCAC[C/T]TTTGTTTCCTTATCT | 286053 |
rs542031737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135115 | TAGAGATGGGGTTTC[A/G]CTATGTTGTCCAGGC | 286053 |
rs542033396 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177556 | ACCCACATCATCTGA[A/G]CACCCACTGTGCAAC | 286053 |
rs542050407 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330275 | TCCATCTCCCGGTTC[A/G]AGCGATTCTCCTGCC | 286053 |
rs542068148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141463 | CATCATTTATTAACT[A/G]TGTCATCTGGGGCAA | 286053 |
rs542078481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101901 | GTTGGATAGTTTAAC[A/G]ATTACAGGTTTTCAA | 286053 |
rs542085386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194495 | TGTTTATTCATTTAC[C/T]AGTTGAAGAACATCT | 286053 |
rs542093055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127452 | TTTAGAAAAATTAGT[A/G]TGGGATTTCATTTCA | 286053 |
rs542098453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125099497 | GAACCTGGGACCCTA[C/T]AACATATGGAGCTCA | 286053 |
rs542101666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360299 | GGACTCAGAACTATC[A/G]ATGTGGATTGGGAGG | 286053 |
rs542102377 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333601 | CTCACTGCAAGCTCC[G/T]CCTCCCGGGTTCACG | 286053 |
rs542118760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237184 | CAGCAGGGACATGAA[A/C]TTACCCCCTGAAAAG | 286053 |
rs542119033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200288 | GGTCTTTACAGTTTG[C/G]CATGTTTTTGCGGTG | 286053 |
rs542149582 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325944 | GCAACAAGAGTGAAA[C/T]TCCGTCTCAAAATAA | 286053 |
rs542158810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227817 | TTTGTGGTTTCTTTT[A/G]GTCTTTTTTTTCTGT | 286053 |
rs542174085 | in-del | -/T | 0.133777 | 0.221342 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196203 | TAACTTTTTTTTTTC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs542223094 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198880 | CCCTGTTATTGGTCT[A/G]TTCAGAGATTCCACT | 286053 |
rs542233653 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261983 | ACACCTGTCATCTCA[A/C]TTACTCGGGAAGCTG | 286053 |
rs542234304 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299936 | TGATTCTCTTGCCTC[A/C]GCCTCCCAAGTAGTT | 286053 |
rs542240485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252958 | ATTTTCTTACCTATA[A/G]AACACAGATTAAAAG | 286053 |
rs542249463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291705 | GTTTTTCTGGAGTTA[C/T]ATTAGTATTTTTGTT | 286053 |
rs542257148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214373 | AACATCAGGTCCAAG[C/T]CTCTAAGACCAGGAA | 286053 |
rs542269938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342709 | AGGTTTTTGTGGGGT[A/G]TGTTTTCTGTTAGGC | 286053 |
rs542271619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136012 | GATACTAAGGTGGGC[A/G]TTTATATGGCTTACC | 286053 |
rs542277350 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258736 | GTAATGGAGAGAGGT[A/G]GGGGGGTTATGGGAG | 286053 |
rs542285669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152135 | AGTAAGCTTTTTTTA[A/G]TGGTTAGTATTTAAC | 286053 |
rs542286275 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166359 | GCAACCTCTGCCTCC[C/G]AGGTTCAAGAGATTC | 286053 |
rs542306528 | snp | C/G | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092831 | GATCCAAGAGAGATT[C/G]ATTTAAACCAGTTAT | 286053 |
rs542322905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221517 | CCAAAGTTCTGGGAT[C/T]ACAGGCATGAGCCAC | 286053 |
rs542344823 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144764 | CTCATTCATCATCTT[C/G]TATTCATTGAAGTCT | 286053 |
rs542348446 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311183 | ATCTGTGCACACACA[A/T]CTAGAAGCAGAAGCA | 286053 |
rs542386072 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258603 | CTGGAGGATGGCTTG[-/T]TTTGTTTTTTATAAT | 286053 |
rs542390952 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280969 | TTCCTGAATGGTAGC[A/C]CAGCTGCACAGACCA | 286053 |
rs542391711 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341080 | AGTCACCTCTCCATA[-/T]TTTTTTTTTCTTTTG | 286053 |
rs542393277 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136164 | TCTAGCCCCTGTTAA[C/T]GGCCAGTGGAAGTAT | 286053 |
rs542408526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143146 | TGCATGTATAGATGT[G/T]TGTTGCTAGAGATAG | 286053 |
rs542428579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258594 | TGTGTGCAACTGGAG[C/G]ATGGCTTGTTTTGTT | 286053 |
rs542441026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251267 | GAATAAATAAGCAAA[A/C]AAAAATTCCATTCTC | 286053 |
rs542455077 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365730 | GGCATGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 286053 |
rs542470926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187467 | CTAGACAATATGGAT[A/T]ATTTTCTCTTCTCCT | 286053 |
rs542503466 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237140 | GGCAAATGTGGAGTC[C/T]ACCATGTGGTGCCCC | 286053 |
rs542522455 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123046 | TAAGAATGGGTTAAA[A/T]TTTCATAAAATCAAA | 286053 |
rs542539589 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181305 | AGCCTGTGTAAAGGT[-/C]TCTTGAGAAAAGAGC | 286053 |
rs542559119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159032 | CAGTTCAAATAAATA[A/G]ATAGCACCTCATTCT | 286053 |
rs542567713 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124885 | CTGCAGCCTCCACCT[C/T]CTGGGTTCAAGCAAT | 286053 |
rs542568047 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188682 | TGAGAGACGGCAGCC[A/G]TTTAATTTACTGTTA | 286053 |
rs542576551 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283376 | AACATGACGAAACCC[C/T]GCATATACAAAAATT | 286053 |
rs542586236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202439 | GAGACTGTCTAAACC[A/G]TGGAAAGATAACTGG | 286053 |
rs542592635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307024 | TGCCAGTGGATAAAA[C/T]AGTGTGTTAAAATGG | 286053 |
rs542597610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167144 | AGTAGCTAACTGTTT[C/T]GATTCTAGTGCAAGA | 286053 |
rs542603299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137941 | CATAGTATGTGCTCA[A/G]TAGATGTTTGCTGTT | 286053 |
rs542612591 | snp | C/T | 0.000115318 | 0.00759249 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102377 | CAACTGGTTTCATCT[C/T]CTTCAGTGGTGTAGA | 286053 |
rs542618415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334901 | CTGGGACTACAGGAT[A/G]TACACCACCACACCC | 286053 |
rs542629410 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128078 | GACTAAAATAGACAT[A/G]GCCATTGTGCTTTGA | 286053 |
rs542647597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203037 | TGCTCTGATGAAAAC[A/G]TGAATATTTGTTATA | 286053 |
rs542649425 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095135 | GGATTATAGGCATGA[G/T]CCACCTTTCCAGCCA | 286053 |
rs542649721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196915 | GGCATGAGATGGTAT[C/T]TCATTGTGGTTTTGA | 286053 |
rs542655190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334316 | TGTAGCACAGCGCTC[C/T]AGGCTGTGCTAAGTG | 286053 |
rs542682581 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160900 | TATTAGTAACACTTA[C/T]TTGAAAAAGTAATTG | 286053 |
rs542705364 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195508 | CTAATGAATTAAATT[G/T]TACTTGGTGTCCTGG | 286053 |
rs542706205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293557 | AAGCTCCATGCTAAT[C/T]ATTGTAGGGAACACA | 286053 |
rs542724893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101885 | TTCAGTATGCATATA[C/T]GTTGGATAGTTTAAC | 286053 |
rs542731277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300504 | TAAGCCATATCAAAT[A/G]TGACAAGGCAAATTC | 286053 |
rs542732834 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133485 | TGGCTCATGCCTGCA[A/G]TCCTGACACTTTGGG | 286053 |
rs542736483 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095462 | TTGGCCAAGTGGTGG[C/T]GCGCGCCTGTGGTCC | 286053 |
rs542736491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168607 | CAAGATGGAATGAGC[A/G]AACAAGCTCTCTGGG | 286053 |
rs542741435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201943 | TCCCCCGCCTTCCTG[C/T]GAAGCTTCAGCCTCG | 286053 |
rs542752785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344369 | CTAGTGCAAATATGC[A/G]GTAGTTATGTCACCC | 286053 |
rs542766396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182588 | CAATGGTATCGTTCA[A/C]GTTTTAAACTGCTGT | 286053 |
rs542777201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107911 | TGGTGGTGCACACCT[G/T]TAGTCCCAGCTACTC | 286053 |
rs542794302 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191853 | GAAAAGTACAAGTTC[C/T]GTTTTTAGCAGACTG | 286053 |
rs542798030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161578 | TGAGGCGGTTGGATC[A/G]TCTGAGGCCAGGAGT | 286053 |
rs542818843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207721 | GGTGAGTCTTCTGCC[A/G]GTTAGGAGGGGCTTC | 286053 |
rs542822936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304756 | CAGCTGCTTGGGAGA[C/T]TGAGGCATCAAGTCT | 286053 |
rs542823734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279596 | CCTAAGTGGCAAAAT[A/G]CGAAAGATAGAAATG | 286053 |
rs542829740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175448 | AAAGCAAACTGCTTA[C/T]CACTAGTATGTGTCT | 286053 |
rs542839955 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154896 | CCTTGCTTTCTACGC[-/T]TTTTATTAAGTACAT | 286053 |
rs542858904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290983 | AGGCATTCAGTAAAT[A/G]TTCAGTAAATATTGG | 286053 |
rs542886240 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304072 | TAAGATATTAATTCA[C/T]TGTACTGACATATAT | 286053 |
rs542886532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311656 | TGTCAGCTGAAATCA[C/T]CAGGGATTTCCCCTT | 286053 |
rs542887422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166351 | AGCTTACTGCAACCT[C/T]TGCCTCCCAGGTTCA | 286053 |
rs542897006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181857 | CAAGTTAGTAGGATC[A/T]TTGAAGGGCCACTAG | 286053 |
rs542897281 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162637 | ATGAGATAACATTAT[C/G/T]TGAAAGTACTTGGGA | 286053 |
rs542900024 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308931 | TAACGTGGGGCCAGC[A/G]TGCAGCTGTCCATGA | 286053 |
rs542905388 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158791 | CCCACTAATTGGCAG[G/T]GGTGCTGAATGGGCT | 286053 |
rs542908033 | snp | A/G | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196276 | GTTACATAGGTATAC[A/G]TGTGCCATGTTGGTT | 286053 |
rs542917855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115356 | CTTTAAAAGTAACAA[A/G]GCCTATATATTGGAG | 286053 |
rs542957141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313146 | AGGAAGGAGAAAGAA[A/G]GAAGGAAGGAAGGAA | 286053 |
rs542958558 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174640 | ATTCAAACTAGACAA[A/G]TAACATTCTTACCCA | 286053 |
rs542962718 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365814 | GTGAGCTGAGATCAC[A/G]CCACTGCACCCCAGC | 286053 |
rs542975787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131356 | GAATGAAGCTGCAGT[C/T]AGATTTATAGGTCAG | 286053 |
rs542981352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210314 | TCATGTAGAATAGAT[A/G]ATTGCTTTCTGATAT | 286053 |
rs542991446 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139443 | GCTAATAAAGACATA[C/T]CGGAGACTGGTAATT | 286053 |
rs542994556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261240 | GGAGCAAGTTTATGC[A/G]AGCTAATCCCCTGCT | 286053 |
rs542995402 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275125 | GGTATGATAGTCATG[G/T]GTCAGCTGATATCAA | 286053 |
rs543000539 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272841 | CATATATATACACAC[A/G]TATATACACACACAC | 286053 |
rs543001388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126194 | TCGAGACCAGCTTGG[A/C]CAACTTGGTGAAGAC | 286053 |
rs543014350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162396 | CTCTCAGAATGTAGA[A/G]TTAAACCGTTTTGGC | 286053 |
rs543030464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351211 | CACAAAAATTGGGAA[C/T]TTACATCTTGGGGTC | 286053 |
rs543037164 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301129 | GAACAATCTATGTGA[C/T]CCATTTAGCCTGACC | 286053 |
rs543051767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153975 | TAGGATTAAGTATAG[A/G]CTACTTAAATTATTG | 286053 |
rs543056734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225824 | TTGTAGACAAATTAT[C/T]GTACTGTTTGATGAG | 286053 |
rs543060792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118928 | TAATGGATCTTGATT[G/T]TGTTATCGATTACAT | 286053 |
rs543076662 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358044 | CCACACCTTCAAAAC[A/G]GAATAAGGCCAGGCA | 286053 |
rs543097891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247615 | CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 286053 |
rs543103559 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352399 | GAGAATCGCTTGAAC[A/C]CGGGAGGCGGAGGTT | 286053 |
rs543105389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359376 | TTCCCTCTTTTTGCC[C/T]AGGCTGGAGTGCAAT | 286053 |
rs543135699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125410 | TCTATTATCACAGAG[C/T]GGGTATTGAAGGGTG | 286053 |
rs543138452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262381 | GTGAGCAGAGATCGC[A/G]CCACTGCATTCCAGC | 286053 |
rs543142107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358650 | CTTGTGCTCTTATCA[C/T]GGATTTGTTGCAGGA | 286053 |
rs543176385 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115538 | CACAGATCACCTGAA[A/G]TCAGGAGTTCAAGAC | 286053 |
rs543179218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096661 | TTTTTTTTTTCATAC[A/G]GAGTCTTTTTGTGAT | 286053 |
rs543187173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329975 | TCTCCAGCCCCCTCC[A/G]AAAGAACCATCATTA | 286053 |
rs543190812 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215934 | CAAGAATTGTGTGTT[C/G]GCACACACCTATTGT | 286053 |
rs543218223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097592 | ATTTCCGTGAAGCCT[A/G]TGTCTCCCCTGTTGT | 286053 |
rs543219176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241392 | TACAGAATACATTCA[A/G]TAATAGTGGAAGTAC | 286053 |
rs543220484 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232898 | TGAGTTATTCTCTGA[A/C]AGGAACTAGCAGGTA | 286053 |
rs543226098 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336886 | TCAGTCCTATTGGCA[A/G]CATAGGCATTCATCC | 286053 |
rs543228954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123934 | CCCATTTAAAATGTA[C/T]AATTTTGTGGTTTTC | 286053 |
rs543233741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319552 | GCAGTGGGGGTGTAT[A/G]TCTTTACATATGTAA | 286053 |
rs543241274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286998 | TGCCTCCTCTGTAGG[A/G]TGGTTTTACCACACA | 286053 |
rs543254267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116734 | CTTGAGCTTGCAAGG[C/T]TAGCTTTTCAGAGGT | 286053 |
rs543257824 | in-del | -/C | 0.0755793 | 0.179102 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284251 | TTGTTAAAAAAAATA[-/C]CCCTGAAAGACAGAG | 286053 |
rs543259570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125363853 | ATGCATACCTGGGCC[A/G]AATCACCCTGATCCT | 286053 |
rs543285833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232088 | GTGCTGATGCCGGGC[A/G]CAGTGGCTCATGCCT | 286053 |
rs543290145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328803 | TTATTTTTAGTGGCA[A/G]GGGAGTTATAATCTT | 286053 |
rs543311714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197623 | GTATAGTTCGAAGTC[A/T]GGTAGCCCACAGCTT | 286053 |
rs543315715 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233874 | TAGATCCCTATTGAT[C/T]ATTTATTTAGAAAAA | 286053 |
rs543356689 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258267 | ATTGATAGCTGTGTT[A/G]AAGACAGTGGTGAGT | 286053 |
rs543387901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364328 | ATGTAAAAACTCCTT[A/G]ATCCACAGATCAGGG | 286053 |
rs543394581 | snp | A/T | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089835 | AGAACATGAGGAGGA[A/T]AATAATAACCAAATA | 286053 |
rs543403670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281973 | CAAACTCTAACTCCT[A/G]CAGGGGCCAGGGAGG | 286053 |
rs543423276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235486 | ATGTGTCATTTTTCT[A/G]TGCATAAGCAAGAAT | 286053 |
rs543427773 | in-del | -/TGGCTTGTC | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135918 | TGTGAATTTTAGACT[-/TGGCTTGTC]AATTTCTACAGAGAA | 286053 |
rs543430319 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271992 | TACATTGACAACTGA[A/G]TATTGAATCTGCAGT | 286053 |
rs543438473 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250502 | TACTGTAAGTAAACA[C/T]TTATTAACTAAAAAC | 286053 |
rs543444625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274775 | TCTCTACTAAAAATA[C/T]AAAAATTAGCCAGGC | 286053 |
rs543466835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148867 | AATGTAACTAAGTAC[A/G]GTAAAATGCCTAAAT | 286053 |
rs543477037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276233 | AGTACATTCTCAATA[C/T]AGCCTTCCAGGAAGC | 286053 |
rs543487854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184738 | TTGTACCATGTCTAG[C/T]GGATTTTCTTTCTTT | 286053 |
rs543528101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176746 | TTGTCTTAAAAACCA[G/T]AAAAATGTCTCATAA | 286053 |
rs543532886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366385 | CTCTATTAAAAATAC[C/G]AAAAATTAGCCGGGC | 286053 |
rs543543894 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307877 | ACCCACAGATGTGTT[C/T]GGCTTGACCCACATA | 286053 |
rs543545646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192654 | TACTAATGACTTGCT[A/G]CATTTCATTTCAATT | 286053 |
rs543571026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256724 | AGGTCAGGAGATCGG[G/T]ACCATCCTGGCTAAC | 286053 |
rs543575703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337604 | TTGACTCTAGAAAAC[A/G]ACAGGTTTGGCCGGG | 286053 |
rs543589014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177316 | TGGATTCAGATCTGT[C/T]TGATCCCGAGCTCAA | 286053 |
rs543604791 | snp | C/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104939 | GAGGCAGGAGAATTG[C/G]CTGAACATGGGAGAA | 286053 |
rs543612006 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353040 | ACCTACAATTTTGAA[A/G]TTCCCCACTCAGCCT | 286053 |
rs543617975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346433 | TCTAAAATAAGAGAA[C/T]GTAAGAAGATGAGTG | 286053 |
rs543660497 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148662 | ACCAGCCTTACCCAC[-/T]TTTTTTGACCAGTTC | 286053 |
rs543689802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322121 | ACCTCAAACTGACCA[C/T]TTTGGGAAGCTAAAG | 286053 |
rs543700047 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248663 | ATCTCAAAAAAAAAA[A/T]GTCAACATCATTCCT | 286053 |
rs543704309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249697 | TTTGATTGAAGGACA[C/G]AAGATTCCTTCAAGC | 286053 |
rs543705770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273673 | CTACACTATGATAAC[A/G]ATTCACTGGATTATC | 286053 |
rs543712028 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146724 | TCACAGGAAGGGGAA[C/T]GTCACACACTGGGGC | 286053 |
rs543713167 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288595 | TAACACTGTTCTGTG[C/T]ATCTGAAACTCTTCT | 286053 |
rs543728039 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163345 | TATAATTAGTTAAAA[A/T]TAAAGTCTGAATAAG | 286053 |
rs543759175 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141005 | AGGTAGCCAAAGGGG[G/T]TCTGCGGATATGCTT | 286053 |
rs543762202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193387 | AACACACTTCTGTTT[A/G]AAAATTAGCAAAGGT | 286053 |
rs543762531 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246294 | GTTCAAGCAATTCTC[C/T]TGCCTCAGCCTCCTG | 286053 |
rs543781643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303868 | TAGTGTTTAAAGATA[C/T]ACATTGTTTGTATAA | 286053 |
rs543785529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296619 | CAGGCTGGTCTCAAA[C/T]TCCTGACCTCAAGTG | 286053 |
rs543803078 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091695 | GTTTCCACCCCTCCC[A/T]CAAGGCGGCGGTCCT | 286053 |
rs543805181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099233 | TTGAGGAAAGATAAA[A/G]CAGAAGCAGAAGGGT | 286053 |
rs543810713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339052 | CAAAACTGTTCTATG[C/T]TGGTAATTCACATGG | 286053 |
rs543818962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186260 | GGGTACTGTCACACT[A/G]TCATGGCAGGGTTGA | 286053 |
rs543819794 | in-del | -/TG | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238868 | TCTGCAGTAAGACAC[-/TG]TGGGGTTATTAGTAC | 286053 |
rs543827662 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340559 | TTTTGATCTCCTTAG[A/G]TGCTGAATTATATTT | 286053 |
rs543833674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206755 | AGGTGCTGGATTTTG[A/G]TATAAATCTTCAACA | 286053 |
rs543836328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200934 | GATCTTCAATCACTG[A/G]TATCATTTCTTCCAG | 286053 |
rs543838311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194211 | CAGTTCTATCAATCA[A/G]CCCCCAACAAAAAAT | 286053 |
rs543867442 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180979 | ATAAGCAATTGAATA[C/T]TCCTGGAGTGGTGGT | 286053 |
rs543875696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331463 | GATAATAAAAAGATT[A/G]TAAAGCACTGTGTAA | 286053 |
rs543912335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098567 | TTGGAGTAATTCAGG[C/T]AAGAGATGATGGTTT | 286053 |
rs543922229 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324823 | TCGTGATCCGCCCGC[C/T]TCGGCCTCCCAAAGT | 286053 |
rs543926087 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147022 | ATTATATATACATAT[A/G]TAATCATTGTCATTA | 286053 |
rs543929820 | in-del | -/A | 0.154661 | 0.231107 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232363 | GTGAAACTCCGTCTC[-/A]AAAAAAAAAAAGAAA | 286053 |
rs543935833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166240 | TTATCTTTTCAGTTA[C/G]TGTAGTCATACTAAA | 286053 |
rs543967814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112407 | TGGGTATGTATCCAA[A/G]GGATGTATGTCAAAG | 286053 |
rs543967935 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244629 | CCAGACAACAAACTA[A/G]AAAATTTGGGGTGCT | 286053 |
rs543980309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213916 | TTTATATCTGATCCA[C/T]TTCAACTGTCTTTCC | 286053 |
rs543988578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289755 | GTTTTCTTTCTTGAG[C/T]AGGACCTTAAAAGCC | 286053 |
rs544010281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172462 | TAGTGGCAGCAACAA[C/G]AAAATGTTTCCTCCT | 286053 |
rs544018168 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214426 | AGATCAGAATTGGCA[A/G]GCAAGGAGGCTGAGT | 286053 |
rs544035370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105279 | CCAAATGTTTTAACC[C/G]TACCCAGTCTGTTTT | 286053 |
rs544062552 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198856 | ATTAGTTACTGCCTC[A/C]ATTTCAGACCCTGTT | 286053 |
rs544063039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128428 | TGAAACTTGATGGTT[C/T]ATTGAATATGGAAAT | 286053 |
rs544068790 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301454 | TAATAATAATCGTAC[C/T]TCACTACATGGAGGT | 286053 |
rs544079227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295739 | GAATAGTTGGAGCTT[C/G]AATTTTGTCTCCTCC | 286053 |
rs544084072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178860 | ACAGAGTGAGACTCC[A/G]CCTCAAAAAAAAATG | 286053 |
rs544094224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346961 | TCATTTGGAGGAAAC[G/T]CTTCATTCAGTTTAC | 286053 |
rs544095132 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360338 | ATAGACGAGTCAACC[A/C/T]GCTCAACTACCGTCA | 286053 |
rs544098972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171014 | CTGCTTTGATTAATA[C/T]TACTGACCTCATCCC | 286053 |
rs544100013 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160762 | GTGTTTTCTTAGACA[-/T]TTTATTTAAATGAAG | 286053 |
rs544126652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163992 | CAAGTATGTTGGAGG[C/G]CTTAGCCCAGGTCTG | 286053 |
rs544128668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212590 | ACCGTTGGAAGTCAT[C/T]GCCAGAGTATTAATT | 286053 |
rs544148016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270824 | GCAGGTCAAAACTTC[C/T]GTGCTGATGAGTAAT | 286053 |
rs544161342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187202 | TCTCCCTTCAGATAC[C/T]GCCTATCTTAGATAC | 286053 |
rs544180917 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215190 | GTGCTATCCCTCCCC[C/G]CTCCCCCTACCCCAC | 286053 |
rs544190162 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316972 | TCGTTTTTTTTTTAA[A/G]AGATGGGGTTTTGCC | 286053 |
rs544190199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251389 | ACAATGGAAAATTAT[A/G]TCACGGGTCTTAATG | 286053 |
rs544192401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348538 | CTCATCTTGAATTGT[A/G]GCTCCCATAATTCCC | 286053 |
rs544200173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135868 | GTTGTCTTTTTCAAG[A/G]TTGTTTTGGCTATTC | 286053 |
rs544200581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115095 | CAGTGGACTTTGTAC[A/G]TTTTAGGTTCTCTTT | 286053 |
rs544218325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150694 | GCTGCTATCTTTGAT[C/T]GTTTTCATTAGGAAG | 286053 |
rs544219237 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326408 | ATATATATGTGTGTG[C/T]GTGTATTTGTAGATA | 286053 |
rs544223860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179535 | GATAATGAGTTGAAT[A/G]TTTTTAAATTTCATT | 286053 |
rs544230994 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355178 | AAACAAACACCTCAT[C/G]TGGCCTAGGTGATGG | 286053 |
rs544234700 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100096 | AGTGTATGAGAACTG[A/T]TGCTGATAGGTGGAG | 286053 |
rs544243521 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215752 | TCAGCTTTCTACATA[C/T]GGGTAGCCAGTTTTC | 286053 |
rs544244645 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123132 | CAAATATATATATAT[A/T]TTTTTCTGGCCAACT | 286053 |
rs544251325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290201 | CCATGTCTTATGCTA[C/T]GAAAATGAATGAGAT | 286053 |
rs544273833 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111487 | AGGGATAAGCATTTT[G/T]CTTAAACCTTTCATG | 286053 |
rs544293114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349610 | AAAAAGAAAGAAAAG[A/G]AAAGAAATGTTCCAG | 286053 |
rs544293129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356428 | CCAACTTCTGGGTTC[A/T]AGCGATTCTCCTGCC | 286053 |
rs544318953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366488 | GAGCTTGCAGTGAGC[C/T]AGGATCGTGCCACTG | 286053 |
rs544326536 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236466 | AATATATACATTTTA[C/T]ATAATAAGTATATAA | 286053 |
rs544350437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326540 | TGTTTCTGAGAATTG[A/G]CATTGTGGGATTGTG | 286053 |
rs544357984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316923 | AGCTGGCACTATAGG[C/T]GTGTGCCACCACACC | 286053 |
rs544364796 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093680 | GTGAGCCGAGATCAT[A/G]CCACTGCACTCCAGT | 286053 |
rs544365929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181122 | TGGAGAGCAGCTGCA[G/T]CAAAGTGATAAGGCA | 286053 |
rs544400540 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219776 | AGACACTTTGGGCTT[C/T]GCTGATTGAAAACAC | 286053 |
rs544404850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094135 | CTGAGATTAAGAATA[C/T]TGGGTATGAAGGGGA | 286053 |
rs544406378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120970 | CACATCTGCCATAAC[A/G]AAGGTTGATTGAAAA | 286053 |
rs544406447 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114514 | CATATCCATGTATAC[A/G]TACATACGTACATAT | 286053 |
rs544444556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325843 | TGTCATCCCAGCTAC[C/T]TGGTAGTCTGAAGCA | 286053 |
rs544466672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121490 | GCTAATAATTTTGTT[A/G]GCAGATAAGGCAAAT | 286053 |
rs544475885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233242 | CTACATTCTGGGATC[A/G]TAACATGTAATTTAG | 286053 |
rs544497191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310292 | CCTGTCAGATTTGGG[G/T]CAAGTTATTTAACCT | 286053 |
rs544498287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194607 | CTATTGAGTAAATAT[C/T]CAGGCATAAGATTGA | 286053 |
rs544500492 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133164 | TGCAGATATCCACTA[A/G]AGGATGATAATTTGT | 286053 |
rs544504448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188502 | GACCCACTGTTGCCA[A/G]ATCTTCAGGTTGTTT | 286053 |
rs544507574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354577 | GCTGGAAGCCCCGAG[G/T]CACTGCACCTTAATG | 286053 |
rs544525702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361082 | CTTTTTTTTTTTTTC[A/G]TTTCTTTTTTCTTTT | 286053 |
rs544525920 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346531 | AATTGTAGACCTTCT[C/G]AATGCTGGCTAATCA | 286053 |
rs544531831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334498 | TAGAGGACCGAAGTG[C/T]TGCAGCTCAGGTCAC | 286053 |
rs544534574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220824 | AAATTTTCCATGAAA[G/T]ATATGATGAATGCAA | 286053 |
rs544535330 | snp | A/G | 0.000399281 | 0.0141238 | missense | NSMCE2 | GRCh38.p7 | 8:125151261 | ATGTAAAGGCTGTTC[A/G]ATCTACAATAAATCA | 286053 |
rs544555676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101046 | ATATTTGAACTGACA[A/G]TGAGTTGTACTGTGG | 286053 |
rs544562126 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100634 | TGGCATGATCTTGGC[A/T]CACTGCAACCTCCGC | 286053 |
rs544576841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314590 | CCATTGTGCTTGGCC[A/G]AGCCTTGCATTTTTA | 286053 |
rs544580780 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311742 | TTGGAATAATTCATG[G/T]GAACCTAAATGGTGA | 286053 |
rs544585716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139135 | AAGCTTTGCCATCAC[A/G]CTAAGAGCCAAACAA | 286053 |
rs544586467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238541 | TGTATCAAATAAGTG[C/T]ACTGTTAGCTGGGAC | 286053 |
rs544599812 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283944 | AGATCACAAGGTCAG[G/T]AGATGGAGACCATCC | 286053 |
rs544607501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362775 | CTACCATCAGAGTCT[A/G]TCTCCTCAGTGAACT | 286053 |
rs544626073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174409 | TGTAAAATCAGTTTC[C/G]TTTCTTTTCCACCAG | 286053 |
rs544628136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167224 | TGTGTAGTAAAGCGA[C/G]GTTTATCTAAATATG | 286053 |
rs544636257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207896 | GAGCCGGAGCTGAAG[A/G]GCTCTTGAGGCCTGG | 286053 |
rs544641125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247523 | TGAGGTCAGCAGTTC[A/G]AGACCAGCCTGGCCA | 286053 |
rs544659564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145687 | CAAATGTGTGGCTAA[C/T]AAAAGTGACTTTTGA | 286053 |
rs544663493 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279957 | AAATAGTGTGAACCA[C/T]GTAACAATGTGCATG | 286053 |
rs544671698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272876 | ATATACACACGTATA[C/T]GTGTGTGTATATATA | 286053 |
rs544677185 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300327 | TGGGACTATACCTGG[A/C]TAATTTTTTTGTTTT | 286053 |
rs544719143 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335744 | CAGTGAGATAGAGGA[A/G]ATGAAGAATTTCCAA | 286053 |
rs544722763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146584 | AAAAATGATGAGTTC[A/G]TGTCCTTTGTAGGGA | 286053 |
rs544725022 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277903 | CCAGCTACCAAATAA[G/T]TTTTTTAAAAAGATG | 286053 |
rs544738090 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265519 | AGCCACTGCACCTAG[C/T]CTTTTGCATTAACTT | 286053 |
rs544745228 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214636 | CAGAGAGTTCCCAGA[A/T]ACCACCTTCTCCCCC | 286053 |
rs544752680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188172 | AGGATTCTCTGAAGG[A/G]TACTATTAAGTCTTC | 286053 |
rs544753730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095178 | TCAGTACACATGTGC[C/G]TAGTGCCTATCATAT | 286053 |
rs544757352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272279 | TCAGCCTCCCAAAGT[C/G]CTGGGATTACAGGCT | 286053 |
rs544758405 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199998 | ACTAGGATTGCAACC[A/C]CTGCTTTTCTTGCTT | 286053 |
rs544762304 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322261 | TAGGTCTAGCTACTC[A/G]GGAGGCTGAGGCAGG | 286053 |
rs544763443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237931 | AGAGAGTACTAAGCT[A/G]TGTTACCCCATGACA | 286053 |
rs544764403 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104818 | GAAGCAGGAGGATCT[C/T]CTGAGGTCAGGAGTT | 286053 |
rs544783571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283954 | GTCAGGAGATGGAGA[A/C]CATCCTGGCTAACAT | 286053 |
rs544804454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350485 | GAGCAGAGAGGTTGC[A/G]TATTAATCCATTTTC | 286053 |
rs544807539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279659 | TCTCTTTTTTGAATC[C/T]GAGTTGAATCATAAC | 286053 |
rs544815372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180388 | ACAAGAAGACAGTCC[A/G]TTCCTACACTAAAAT | 286053 |
rs544823047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252484 | TGAGCTGAGATCCCG[C/T]CACTGCACTCCAGCC | 286053 |
rs544827836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333664 | GGACTACAGGCGCCC[A/G]CCACTACGCCCGGCT | 286053 |
rs544829724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125129993 | AGCTCCAGACTTTAT[C/T]TGGATTTCACTGATA | 286053 |
rs544835537 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361142 | TGTCTCCCAGGCTGG[A/C]GTACAACCTCTGCCT | 286053 |
rs544847062 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201992 | CGCTAGCAGTGAGCA[A/G]GGCTCCGTCGGCATG | 286053 |
rs544867708 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153051 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 286053 |
rs544875275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143425 | CAGGCAATCCCTTGC[C/T]GCCTTTTCTTCCTTC | 286053 |
rs544898934 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259951 | CATTGGGCTCATGTA[A/G]TCCAACCTCTTCTCT | 286053 |
rs544902276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253927 | AAAAAAATTTTTTGG[C/T]AGTCATAGTCATCAT | 286053 |
rs544912722 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116541 | TGGATAGTTGCTTTT[A/T]TAATGTTAGAATTGG | 286053 |
rs544913716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305291 | CATTGCCATTTTACT[A/G]CTGTGAAAACCTAAA | 286053 |
rs544939794 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285727 | ATTTATTGAGCACCT[A/G]CAGTATGCTAAGAAT | 286053 |
rs544943403 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259499 | TTTCATCCAGAAACC[A/G]TCGTCGTGTCCTCCC | 286053 |
rs544949548 | in-del | -/A | 0.126564 | 0.217402 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263759 | ATCTCAAAAAAAAAC[-/A]AAAAAAAAAAAGAAG | 286053 |
rs544952769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095799 | AGGCAAGAGAATTGC[A/T]TGAACCTGGGAGGCG | 286053 |
rs544967703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197750 | TTGGTAGCTTGATGG[A/G]GATGGCATTGAATCT | 286053 |
rs544981493 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279077 | TTTATGTTATCTGCC[A/G]TCTCCAAAAGTTTAG | 286053 |
rs544986248 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182833 | TTTGACTTAAGAATT[A/G]GAGCAGGCAATGTAA | 286053 |
rs544998072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293622 | TGAGTAGAGGTAACA[A/G]GATTACCCTAAACAT | 286053 |
rs544998441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301261 | TCGGCATCCAGAAGG[A/G]GTTGAAAAACCAGCA | 286053 |
rs545007375 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226060 | AAATTCAACCTTTAT[A/G]TCTGTTTGCAAAAAA | 286053 |
rs545021705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239695 | TTTAAAAAGAAAAAT[C/T]ATACCACTTCCTTCA | 286053 |
rs545030391 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198297 | GCTTCCAGTTTTTGC[C/G]CATTCAGGATGATAT | 286053 |
rs545040451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364363 | GAAATACTTTCTTTC[A/G]TGTTGGACTGTTGGG | 286053 |
rs545042168 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153784 | AAATGCTTTGGCATT[C/T]ATCAAATTTGATGGG | 286053 |
rs545047608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104098 | CGGGTTCAAGCGATT[C/T]TCCTGCCTCAGCCTT | 286053 |
rs545054544 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280480 | TGTGCAAACTGCTTA[A/T]TTGAAGCAATAAAGC | 286053 |
rs545062262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328317 | GGGATGGAGCTAAGT[A/G]TAATAACTGTAGTCT | 286053 |
rs545063472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147220 | GTCACACTGAAAATA[C/T]AAAATAGGCAAGTGA | 286053 |
rs545064622 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103230 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 286053 |
rs545065101 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162527 | CTGAATAGCTGTGTG[A/G]CCATAAGCAATTTTC | 286053 |
rs545091031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255000 | TAGAATATGGCAGAA[A/G]TGACGCATTGTATCA | 286053 |
rs545092216 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236954 | AAAACTGAATGAGTA[A/C]ATGTACCTTAAGTAG | 286053 |
rs545118212 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163343 | GATATAATTAGTTAA[A/G]AATAAAGTCTGAATA | 286053 |
rs545122537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189199 | TTTACTTTCTGCAGA[A/C]AGGGTGCTCCACACA | 286053 |
rs545132086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294146 | TCACTATTTCATTCC[C/T]TTCTAGTGCTGAGTA | 286053 |
rs545143188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287828 | CTCTGCAGAATATCT[A/C]CAGTGACCTGCACAT | 286053 |
rs545151649 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337669 | GGAAGCCGAGGCTGG[C/T]GGATCACCTGAGGTC | 286053 |
rs545152134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342865 | GCTACATTTTGGGGA[C/T]TTCACCCACATTGTT | 286053 |
rs545158118 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336303 | TACTCAGTTAAATAC[A/T]CAGTCCTTACAGTAG | 286053 |
rs545178007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203109 | GGGCCTTTAATACAG[C/T]AGGGATTCCTTTATA | 286053 |
rs545179063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275860 | AATTCAAACCCAGAA[C/T]GCTCCGCCTGCAAAA | 286053 |
rs545197986 | in-del | -/TCTCTCTT | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213660 | CTCTTTCTCTGTTTC[-/TCTCTCTT]TCTCTCTTTCTCTCT | 286053 |
rs545201542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273320 | GCCTTCCAAAACATT[A/G]TAGTCATGTTACAGT | 286053 |
rs545202047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298973 | ACTTCCTTGCCCCCA[A/T]TTATTGCTGAAACAT | 286053 |
rs545203830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267147 | GTAACTGGATTATAT[A/G]TAGGCACGCACTGCC | 286053 |
rs545207801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169282 | TGAGAAATAGCATCT[A/G]TGCTCATAACTTGAA | 286053 |
rs545216820 | snp | A/G | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092260 | ACTCTCTGGACCTCA[A/G]TTTCCTCTTCAGTTA | 286053 |
rs545228275 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186729 | ACAGAAAGATTTTGA[A/G]GCTGGGTTCAGCCCC | 286053 |
rs545242328 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301984 | TTTTTTTTTGAGACC[A/G]AGTCTCACTCTCTTG | 286053 |
rs545254187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159992 | GTTCAGTTGGTGCCA[A/G]TAGTATGTTTAGTCC | 286053 |
rs545256948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300556 | TCTCAGTAAGTTGGC[A/G]CTGTTCCATTCAACA | 286053 |
rs545257461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196162 | GTGCTGGGATCACAG[C/G]CATCAGCCACCAAGT | 286053 |
rs545258097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313964 | AAAGCCCTGCATGAG[C/T]AACTTTAGGCTATCT | 286053 |
rs545264339 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174587 | CCTCATTCAGCTTCC[A/G]TCTGTTAGACAACTG | 286053 |
rs545264723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335042 | ATTACAGGCGTGAGC[C/T]GCAGTACCTGACCAG | 286053 |
rs545291523 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189947 | TTTGCTGGCTCTTCT[A/G/T]TGGTTTTACCATCTC | 286053 |
rs545294407 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167727 | GCTAGACTTGGGGGG[A/G]AAAATCAGTGGAATT | 286053 |
rs545308641 | in-del | -/TTTGT | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125363944 | GGCACTTTTTTTTTG[-/TTTGT]TTTGTTTTGTTTTGA | 286053 |
rs545319719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210537 | CTATAGAAGAACTGT[A/G]GAAAGGGAAGTAGCA | 286053 |
rs545337773 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291842 | AGGAGTTTCTATATA[A/G]ACAACTCCAAAACCC | 286053 |
rs545341169 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168664 | ATTAATGAGGGCTTT[A/G]CCCTCGTGCTCTAAT | 286053 |
rs545342979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255560 | TGTGATCACAAGCAG[A/T]GAGGAAGGAAACAAC | 286053 |
rs545353194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203835 | AGGGTTTTCCAAAGT[A/G]AACATAGTCAGGTTA | 286053 |
rs545361068 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355525 | GCCAATATGGTGAAA[-/C]CCCATCTCTACTAAA | 286053 |
rs545364692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175707 | TGAAACGATGGTTAT[A/G]AGGCAATAATGATAA | 286053 |
rs545373147 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150680 | AGTCACCACGCCCGG[C/T]TGCTATCTTTGATTG | 286053 |
rs545375161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155466 | AATGTTTATAGAATA[A/G]TTGAGTAACCTAAGA | 286053 |
rs545377620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124719 | CTGGGGTCAAGCGAT[C/T]CTCCTGCCTTGGCCT | 286053 |
rs545377967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218564 | TTACAGGCACCTGCC[A/G]CCATGCCTAGCTAAT | 286053 |
rs545382200 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101307 | AATGATGAGGATGGA[A/C]ATGCCAGAGATACTA | 286053 |
rs545397056 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104669 | TATCTGCATAGCTCC[C/T]TCACTCTCTTGCAAA | 286053 |
rs545399905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307081 | CAGATCAGCTCCCTG[C/T]TCACTTAACATGGAG | 286053 |
rs545404010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357885 | GAGGTGGCGTGTTCA[C/T]GCTAGAGGAAGAGGC | 286053 |
rs545426846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352299 | CCTGACCAACATGGA[A/G]AAACCCCGTCTCTAC | 286053 |
rs545434244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212502 | CAACAAGGTGAAAAG[A/G]GCAAAATGGGCAAGG | 286053 |
rs545440480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315890 | TCACGGCAGCTTCAA[C/T]CTCCTGGGCTCAAGC | 286053 |
rs545447382 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143718 | AGGACCAAATTTCAG[G/T]AAACAGCTTGGCCGT | 286053 |
rs545468050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308966 | ATTGTGTTATGAGGC[C/G]GGGCACGGTGGCTTA | 286053 |
rs545489547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210998 | TTGGCCTCCCAAAGT[G/T]CTAGGATTACAGGTG | 286053 |
rs545506396 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120728 | ACTGGCTTTCTCTCT[A/G]TGGGTGGGAGTTATG | 286053 |
rs545514754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219197 | AGACAGAAAGAGATG[G/T]AAGAAAAGCCTGAGT | 286053 |
rs545522584 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204698 | CCTACTGCAGAGATG[C/G]GTAAGAATTATGCCA | 286053 |
rs545553527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192521 | ATATTATATGTATAT[A/G]GTAGCAAATAGGGAA | 286053 |
rs545581415 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343256 | GTGACAACTTATAAC[A/G]CAGGTACTTCCTCCT | 286053 |
rs545584694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117446 | CCTTCCTAAGATACC[A/G]TAATTTGCCATGTCT | 286053 |
rs545597759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357413 | TTTGATTTCACTTAG[A/G]GAGTTAAGGAGGGAG | 286053 |
rs545599385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225514 | AAAATCATCAGCTCA[C/G]CCTGTTTGCATATCC | 286053 |
rs545601242 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216533 | AATCCCAGCTACGTA[C/T]TGAGGCAGGAGAATT | 286053 |
rs545604565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302037 | CAATCTCAGCTCACT[C/G]AAATTCTGCCTCCCA | 286053 |
rs545614657 | in-del | -/TT | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093971 | CTGTGTAAGTTTAAA[-/TT]TTTTTTTTTTTTGTA | 286053 |
rs545624829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262979 | TCTTGAACTAGATCT[A/G]TATGTTTATGCTGGT | 286053 |
rs545653425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234403 | GTGAAAACTAGGCAG[C/G]CTTTTTCAAATATAT | 286053 |
rs545661438 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261575 | CTTGAATTCTGGAAA[C/T]TTAATTAATATACTT | 286053 |
rs545682524 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097893 | ATACTGTGCTAATTA[C/T]GTTGAATTTTATTAT | 286053 |
rs545685611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132792 | GAGCCACCCACACCC[A/G]GCCCAATTTTTAAAT | 286053 |
rs545686337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281287 | TGCTTTAATATTGGA[A/G]ACATTCTAGTTTTGG | 286053 |
rs545694168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177444 | TCTTGTTCCTCCTTT[A/G]CCATCAAACTATATT | 286053 |
rs545709405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351778 | CACTTTGGGAGGCCA[A/G]GACAGGCAGATCACT | 286053 |
rs545720860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330396 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 286053 |
rs545727637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090703 | AATATTTCTTAAGGA[A/C]ATCGAATTGTCGTGG | 286053 |
rs545737120 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244031 | GAAGATATTGTAAGA[A/G]TTTTTTTTTTAAGTA | 286053 |
rs545766543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237002 | ACTCAGTAGTTATAC[A/G]TTTCCTCTGAGGCTC | 286053 |
rs545798768 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269193 | CCTGGGTTCCAGTGA[G/T]TCTCTTGCCTTAGCC | 286053 |
rs545806059 | in-del | -/TTAATGTACCTCAAAGATGTAAACTACATCT | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110105 | CCCTTCTCTAAAATG[lengthTooLong]TTGTAGTTTTCAAAG | 286053 |
rs545821357 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269484 | CAAAACCATGCCACT[A/G]TAAAATGACACTCCT | 286053 |
rs545825765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164208 | TCCCTTTAATAAGCA[C/T]AGTGACCTTACAAAG | 286053 |
rs545827331 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117178 | TAGCATTAGGGTAGC[C/T]GCTGCTTAATTTAAA | 286053 |
rs545829698 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125367080 | CATATTGTTTATTTT[A/T]AAGTGTTCTATAATG | 286053 |
rs545830116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244289 | CAAAGTTGAGCAGTA[A/G]CAGAGTAAAAATAGG | 286053 |
rs545830762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323959 | AAAACTCAATAAGAA[A/G]AAAGCACTCCCAAAA | 286053 |
rs545867831 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354423 | TATGTATTTTCGATT[A/C]CCGGATCAACAATTA | 286053 |
rs545869453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178112 | TCCCTCCCTCTCAGT[G/T]GTGTGTCCTCCAGGC | 286053 |
rs545870180 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237781 | AATACTACCTTGTGG[A/C]CATCTGTTGGCACAG | 286053 |
rs545873113 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270912 | ATCTCTTAGAAAAAA[A/G]AAAAAAAAGAATAAA | 286053 |
rs545888241 | in-del | -/T | 0.245346 | 0.249957 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183411 | AGTTTATTTTTGTTC[-/T]TTTTTTTTAACATCA | 286053 |
rs545893991 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349528 | CCAAGGTGGAAGGAT[C/T]CCTTGAGGCCAGGAG | 286053 |
rs545897034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263574 | TGCCAACATGGTGAA[A/G]CCCTGTCTCTACTAA | 286053 |
rs545905802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143097 | CCCAGTGTGGGTGCA[C/T]GCACACACACACACA | 286053 |
rs545908465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309584 | AAAATAATTAGCCAG[C/G]CGTGGTGGCACATGC | 286053 |
rs545922665 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187374 | ATTCTCACTAGCCCA[A/G]GTTGTGAAATGAAAC | 286053 |
rs545929461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150623 | CTGACCTCAAGTGAT[A/C]TGCCTGCCTCGGCCT | 286053 |
rs545937780 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361259 | TTTTAGTAGAGACAG[A/G]GTTTCACCATGTTGT | 286053 |
rs545948963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250555 | TTATATTCTCATGAA[C/T]TCAGATTTGTCTTAA | 286053 |
rs545955530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347723 | AGACAGTGGATATTA[C/T]GAGATTTCAATGAAA | 286053 |
rs545955564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339125 | GTTGGAGGAAGGGAC[A/T]CTGCTCTGCAGTGTC | 286053 |
rs545962282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277516 | CTTCTTCTTCTTTTT[C/T]TTTTTTTCGAGATGA | 286053 |
rs545966496 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270175 | TATGACTTACTAAAG[A/G]ATCTGAAAGGTCCAG | 286053 |
rs545968864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171109 | AGGTCTCTGGTTCAG[A/G]TGTCGTCTTTTCATT | 286053 |
rs545971206 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246071 | TATATAACCATAGAC[C/G]TGTTGGGAATTTTTA | 286053 |
rs545980448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099844 | GCTGGTAACCAGAGG[A/G]GTAAGTGGGAGGAAA | 286053 |
rs545989290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243118 | GAGTGAAAAAGACAT[C/T]GGCTCACCCCTGAAA | 286053 |
rs546001254 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141221 | CAAAGATGTCGTGGT[C/G/T]TCCATCACTCTGAGG | 286053 |
rs546001556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133881 | ATCATACATTAGAAC[C/T]GTGGATCTCAAATTT | 286053 |
rs546001773 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185301 | GCTCCCATTACATTT[A/T]AAATTTTTTTTTTTC | 286053 |
rs546046820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277513 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTCGAGA | 286053 |
rs546052123 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347673 | CATGAAACAACAGAA[A/T]AAGAAAGAAGTTTGA | 286053 |
rs546072408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366471 | TGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 286053 |
rs546074365 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271735 | AGGATGCATGCTTGA[-/T]TTTTATTGCTTTTGA | 286053 |
rs546077531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097803 | GGTTATATGAAATGT[A/G]TGATTTAAGTCTTGG | 286053 |
rs546085758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235133 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCGG | 286053 |
rs546088732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275509 | TGAGTTCTCTTCCTC[A/T]TACTGCCCTCTAACT | 286053 |
rs546108404 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281894 | AAGTGGGTGATTTAA[A/G]AATCTTAGAAGGCTC | 286053 |
rs546126749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365996 | GCACCAAGCTGGAAC[A/G]TCCTCAGCACTGCAC | 286053 |
rs546132995 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140664 | AAAAAAAAAAACATA[C/G/T]GAGATTTAAGCCTCA | 286053 |
rs546144464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156647 | TAACCTGAACATTTT[A/G]TATGCCTTTTAAAAC | 286053 |
rs546149292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325897 | GCGGAGGTTGCAGTG[A/G]GCCAAGATTGCGGCA | 286053 |
rs546158074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187633 | TTCATTTACCTGTTA[C/T]GTGACTATCAGGCCC | 286053 |
rs546160711 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332113 | CAAATCGACATCAAG[A/C]ACAGGAGTTGTACTC | 286053 |
rs546171792 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266685 | TCATGAGAATTTCAG[A/T]TCCAGTATACCTGTT | 286053 |
rs546171863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187295 | GATGACTAGGATAGT[A/G]ATGGTGGTGATAACT | 286053 |
rs546175163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251189 | ACAAAGCAGATAAAT[A/G]TCAATAGCTTTCTTA | 286053 |
rs546177421 | in-del | -/AGGT | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118315 | CCTGCCAGGAGGCAG[-/AGGT]TGCAGTGAGCCGAGA | 286053 |
rs546185903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283326 | GGCTTAAGTGGGTGA[C/T]CACTTGAGTCCAGGA | 286053 |
rs546190257 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205798 | TATAGGTTGTAAATA[C/T]CAGTATCGTACTTAA | 286053 |
rs546194073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179556 | AAATTTCATTTTGAT[A/G]GCTAGAGTACAGTCA | 286053 |
rs546246281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333703 | TAGTTTTAGTAGAGA[C/T]GGGGTTTCACCATTT | 286053 |
rs546250113 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093390 | TAAGATGTGGGCAGA[C/T]AGAAAACTGAAGAGA | 286053 |
rs546289986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194256 | TTGTAGTTGACTCCT[A/C]CCCCCATTCCCAGCC | 286053 |
rs546311146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193931 | GTTGATTTATTTGCC[A/G]GGTCCTTGTCACTTT | 286053 |
rs546324113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276848 | ACTGACCTGCCAAAT[A/G]CCATCTCTTCTGGAA | 286053 |
rs546346782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199701 | TTAGGTCTGCTTGGT[A/G]CAGAGCTGAGTTCAA | 286053 |
rs546352543 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150853 | TGGGAGAGGTGTAGT[A/G]ATTGATTTAAGATCA | 286053 |
rs546359812 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196767 | TTCTAGATCCTTGAG[A/G]AATTGCCCAACTGTC | 286053 |
rs546370231 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232371 | TCCGTCTCAAAAAAA[A/G]AAAGAAAGAAAGAAA | 286053 |
rs546375089 | snp | G/T | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362220 | ATGCCGAATGCTTAC[G/T]GAGACAGTTGTTTCT | 286053 |
rs546375892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296010 | GTATGAGTAGGAATT[A/G]CAGCTTACAGCTTAG | 286053 |
rs546387891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099356 | ACCTTAGAGAAGTAA[A/G]GGAATTGACCTAGTA | 286053 |
rs546415148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295847 | TGTTTTGAGCATTCT[A/G]TTGACTAAAATATTA | 286053 |
rs546419676 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142259 | TCTGAAGTAGTTACT[A/G]TTATTGTACCCATTA | 286053 |
rs546427276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193813 | GTGTGCCCCTTCAGT[C/G]TCTGCCTATCACTGA | 286053 |
rs546432227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257796 | TCTTCGGCCTCCCAA[A/G]GTCCTGGGATTACAG | 286053 |
rs546454738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206280 | AAGATTACAAGGGTA[A/G]GTTGGGACAGATTTA | 286053 |
rs546464225 | in-del | -/T | 0.00159776 | 0.0282193 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177012 | TTGCAGACTTCTCTA[-/T]TTTTTTGCCCTAGTA | 286053 |
rs546493097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164653 | AGAAAAACTTTTGAA[C/G]AGCCAGTATTATTTA | 286053 |
rs546497762 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156987 | GGAAGAATTTCTCCC[C/T]TAGAAAGCTAATAAT | 286053 |
rs546504411 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240386 | CCTTGGCCTCCCAAA[G/T]TGTTGGGATTCCAGG | 286053 |
rs546511846 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164240 | TAGGAAAGGTGGCTA[C/T]TGTTGACTCTGAGCC | 286053 |
rs546512323 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133729 | GCGAGACTCCATCTC[-/A]AAAAAAACAAAGCAA | 286053 |
rs546516016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200459 | GCTGGATATGAGATT[C/G]TGGGTTGAAAATTAT | 286053 |
rs546532874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134160 | TCTTTCATATTTGTT[A/G]TGTAAAAAATCTGTA | 286053 |
rs546545748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101395 | ACTGTATGCTATACC[A/G]TACCATGGTTATTCC | 286053 |
rs546547397 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339783 | TGGCCCCCTGAGCTT[A/G]CCTCTCTCCTGGTGC | 286053 |
rs546552059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289083 | GCATGTGCCACCACA[C/T]TTGGCCTTTTCCCCC | 286053 |
rs546557842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108729 | AAAGATGGATGAGTT[C/T]GGAAGTCTGTGTAAG | 286053 |
rs546569147 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251550 | GGAGTTTGAGTGAGA[A/G]CTAGAAAATAGATTT | 286053 |
rs546573117 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130684 | ATGTGTATGTAGGCT[A/G]ATGTATGTGTACATA | 286053 |
rs546573665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283600 | ACTGGAAACTGCTTA[A/G]TTAACCTCTGTGAAT | 286053 |
rs546598149 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347170 | TACCATTAGTATCTC[C/G]ATTTCATAGCTGAGA | 286053 |
rs546604521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179979 | CCTGAATGTCTTCCT[A/G]TAATGTTACCATTAA | 286053 |
rs546628691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125847 | TCACCTTGTTGTCCC[C/T]TCTGTCCCAAGTCCT | 286053 |
rs546632605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252627 | TTATCAATGAGGTCT[C/T]GTAATTGGCAGTACA | 286053 |
rs546641528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207358 | AGTGATATAAATGAG[A/G]TATACACATTTATTA | 286053 |
rs546647229 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142724 | ATTCTCCTGCCCCAG[A/G]CTCCCGAGTAGCTGG | 286053 |
rs546656894 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278422 | GCCCCAAGGGCAGTA[C/T]GCTAGTGCAGAGGAA | 286053 |
rs546657201 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105958 | GGGAAAAAAAGTGAA[C/T]TAAACAACTTAGACA | 286053 |
rs546659474 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092648 | GTTGAAAAAGGAGAG[A/G]CAGCTCTGGCTGACT | 286053 |
rs546676035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229306 | AGTGAAGGCAACCTA[A/T]GTTACATTAGATTCG | 286053 |
rs546678329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246404 | GGTCCAGCTGCTCTC[A/G]ATCTCCTGACCTTGT | 286053 |
rs546686449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343001 | TTTAAACGAGTATAT[C/T]GTGCCACTAGAAAGA | 286053 |
rs546694863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108205 | TGAATAGGAGGTAGA[C/T]GACATGAGAAGTCCT | 286053 |
rs546697035 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194104 | CTCTCCCATCTATTA[C/T]CTTATTTAATTTTCA | 286053 |
rs546702769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208036 | GGTAGAAAATACTGT[G/T]GCCAGATTGTCAGTC | 286053 |
rs546710503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277300 | GCTCCTGAGAAAGGT[A/G]TCTCCTCCTCAAGTC | 286053 |
rs546715905 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238015 | GTATGGATGAAGAGA[A/C]TATATATTGTAGATG | 286053 |
rs546718131 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195674 | GTCTCTATGCTCATG[G/T]AGCTTACATTCTGGC | 286053 |
rs546721339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342472 | TTTGCATGTGGGGAG[A/G]ATTTTAAAGGGATGG | 286053 |
rs546724399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304842 | ACAGTGAGCTGAGAT[C/T]GTGCCACCTCATTTC | 286053 |
rs546751679 | snp | C/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122046 | TAGGCCTGTGCTCAG[C/G/T]GTAGATAGCTCTTTT | 286053 |
rs546761525 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311340 | CTTTGTAGAAATCTG[A/T]AAAAAAAAATGCGTA | 286053 |
rs546782258 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227190 | ATTGGGGGGCAGCCT[C/T]CAGATCCACAAGACA | 286053 |
rs546784650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106561 | TGCGCACCTGTAATC[C/T]GAGCTACTCAGGACT | 286053 |
rs546785291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150085 | CAGGCTGCTGCAAAT[C/T]CAGGAGGACTGCCTT | 286053 |
rs546789267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257582 | TCTGTCGCCCAGGCT[A/G]GAGTGCAGTGGCGCG | 286053 |
rs546837945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347492 | TCTGTCTCTCCTACC[A/G]GACCCGATCTTATTC | 286053 |
rs546843749 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224390 | GCTCAGCCCAATGTC[A/G]TGGAGCTATTCCTAG | 286053 |
rs546845974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106997 | CAAAATTCTGTCTCA[A/G]AAAAAAAACAACAAA | 286053 |
rs546847373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348871 | AATACAGGAACCTAG[A/G]ATTCAGCTTCCTGCA | 286053 |
rs546853214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221803 | TGCATTTTGACTGCA[A/G]CTAGGTGTGGAATTT | 286053 |
rs546859189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122452 | ATGATGTCACTGGCT[A/G]TATCCCCTTATACTC | 286053 |
rs546868604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212805 | CACTAAGGAGGCAGA[A/G]GGTGACTAGATTTCA | 286053 |
rs546907173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244051 | TTTTTTAAGTAGCAT[A/G]GAATTAATTGTGACT | 286053 |
rs546911461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340709 | TCTACTTTTGGTAAC[A/G]AAAATAAAATTCTCT | 286053 |
rs546948155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339910 | GGAAAGTTGCATGAG[C/T]CATACCTTGGGCTCC | 286053 |
rs546950206 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203021 | ACCATGAACCTTCCT[A/G]TGCTCTGATGAAAAC | 286053 |
rs546972178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364523 | GATCACTGGGCCAGA[G/T]CTCTGTGTGGGCAGG | 286053 |
rs546972229 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124791 | CCTCCTCAGGATTTT[C/G]TTGTTGTTGTTGTTG | 286053 |
rs546990840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266743 | GGAGTTTGGGATTAG[A/G]AATAGAAGATAAAAG | 286053 |
rs547013606 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276670 | AGGAAGGAGAAAGGG[A/G]AGGAATGGTGGATTT | 286053 |
rs547016900 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301355 | AATAGAATGCAGTGG[C/T]TCATGGTATCCAGCA | 286053 |
rs547019753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297707 | AGGCATAATAGCGTG[C/T]GCCTGTAGTCATAGC | 286053 |
rs547059736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116849 | GCCATACTGAAGATA[C/T]ATCTCTTGATCCAGT | 286053 |
rs547075167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285263 | TTATACCAGAGCTTA[A/G]GAGAATAAAAATAAG | 286053 |
rs547077118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291983 | TTCTGTCCTCCCGCA[C/T]TCAATTCATTCAAGC | 286053 |
rs547086601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201194 | TCAAAGTCATTCTCC[A/G]TCCAGGTTTGTTCCA | 286053 |
rs547101438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159284 | AGGATAAAACATAGT[C/T]ATACAGTCATGAACC | 286053 |
rs547119838 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302448 | AGTAGGAGATGAGAT[C/G]AGAGAGCTAACAAGG | 286053 |
rs547130763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267164 | AGGCACGCACTGCCA[C/T]GCCCGGTTAATTTTT | 286053 |
rs547131626 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359419 | GCTTACCACAACCTC[C/G]GTCTCCCAGGTTCAA | 286053 |
rs547155200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239906 | AGTCAGAGAAAGATG[A/G]TCACCTGAGAAGTAA | 286053 |
rs547163083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160211 | TGATAATTTAGGTCA[A/C]AGAGTTTCATTAAGG | 286053 |
rs547174142 | snp | G/T | 0.000577423 | 0.0169817 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155951 | AACAAGTTCAGAGAT[G/T]ACTGTCATATATATT | 286053 |
rs547182798 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164299 | CACTTGGTTAGTCTC[-/AA]GAGGTGAGACTTGAA | 286053 |
rs547187802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138618 | GTCTTCGTTGTTTAA[C/T]TTATGGCTGTAATTA | 286053 |
rs547201902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362303 | CCTTTCTGCTTTAAA[A/G]ACTTGTGTTTATTGG | 286053 |
rs547210776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221134 | CATATGGCTTGAAAA[A/T]TAGCTCAACAAAGTT | 286053 |
rs547219895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271674 | GAATAGGTATGAATC[A/G]GGTTTCATAGGCAGG | 286053 |
rs547223406 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283950 | CAAGGTCAGGAGATG[A/G]AGACCATCCTGGCTA | 286053 |
rs547246061 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328413 | ATAAAAGCACATGGA[G/T]AGCTATGAACGTGCA | 286053 |
rs547264076 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172789 | TTCTGAATCCAAAGT[G/T]GGTATTTTTAATTCC | 286053 |
rs547280153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304431 | AGTGCCCCGTGATGT[A/T]TGTGCTAAAGTGTAG | 286053 |
rs547312307 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094085 | CTGGGATTATAGGCA[C/T]GAGCCACCACACCCA | 286053 |
rs547318902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355409 | TGTTTAGAAAGCTAC[G/T]GATCTTTTGGCTGGG | 286053 |
rs547323073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175999 | ACTTAGTTCCTAACA[G/T]TCAACTCATTGATTA | 286053 |
rs547324007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138158 | AGATTGTAAAAGTCA[A/G]CAGTACTAATATAGG | 286053 |
rs547333524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125130080 | ATCATCTTCGTAGAC[A/G]CTTCTTAGTTGGTTT | 286053 |
rs547334375 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206278 | AAAAGATTACAAGGG[C/T]AAGTTGGGACAGATT | 286053 |
rs547347110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272757 | TATATATACACACGT[A/G]TATATATATACACAC | 286053 |
rs547351151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356938 | AAGAGATCACCAGGT[C/T]GGTTCTCTGACTCTG | 286053 |
rs547355793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094774 | CTTCTTGGCTTGTAG[A/G]TGGCTGCCCTTTTTA | 286053 |
rs547366247 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096907 | GAGCCACCACACCTG[A/G]CCCTCTGTGTAGAAT | 286053 |
rs547379030 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217880 | GACCATCTAAATATG[-/A]AAAAAAAAAAAAACC | 286053 |
rs547384268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313453 | GGAAAACACTTTAAA[A/G]AAGGAAGGATCTGTA | 286053 |
rs547385612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168678 | TGCCCTCGTGCTCTA[A/G]TCTCTTCCCAGAGGC | 286053 |
rs547400167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320996 | AGAGAGAGGGGCTAC[A/G]CACTTTTCAACCACC | 286053 |
rs547404417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209071 | CTCGTCTCAGTCTCC[G/T]GAGTGGCTGGGACTA | 286053 |
rs547414283 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117548 | TTTTATTTTTATTTT[A/T]TTTTTTTAAGAGATG | 286053 |
rs547419411 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128460 | GAGGAAAAGGAAGAA[A/G]TCAATGGTGATACTC | 286053 |
rs547427686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322240 | AGGTGTGGTGGTGGG[C/T]ACCTCTAGGTCTAGC | 286053 |
rs547435962 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147315 | ATTTTAGTGAAAGTT[C/T]AATTTTCAGATTTAT | 286053 |
rs547447377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312840 | AAGAGTACGGGGCCG[A/G]TTGGAGAAGAGTCAT | 286053 |
rs547469516 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215382 | GAACTCATCATTTTT[C/T]ATGGCTGCATAGTAT | 286053 |
rs547480745 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137222 | CTCCCCACAAACTAC[-/T]TCTTATTTAGATGGA | 286053 |
rs547484206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330109 | GATTCGGGGCACGTC[A/G]CTTTCAGAAGGATGG | 286053 |
rs547507136 | in-del | -/TTG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124788 | AGCCTCCTCAGGATT[-/TTG]TTGTTGTTGTTGTTG | 286053 |
rs547520432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306667 | AGCCTTCATATTGCA[C/G]AGTGAATAACCCAGT | 286053 |
rs547523045 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281407 | ACACATTATACAGCA[A/T]GGTTGCCAGAGGAGA | 286053 |
rs547532812 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245411 | TTAAAAAAGAAACTT[A/G]TCTATAACACAAGTC | 286053 |
rs547536684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268214 | ACTCCAGCCTGGGCA[A/G]CAAAGCAAGATGCTG | 286053 |
rs547540107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095245 | AAGTTCTATTGGACA[A/G]TGCTGCTCTGGACAA | 286053 |
rs547540150 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184949 | GAGAGAGAGACTTGC[-/T]TCTAGATGCCTGTTT | 286053 |
rs547568338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278583 | TACTGATTATACAGC[A/G]AACATGTTGATGATA | 286053 |
rs547596101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154895 | TCCCTTGCTTTCTAC[A/G]CTTTTATTAAGTACA | 286053 |
rs547596626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246930 | AAAATACTTAAGATC[A/G]GCATTCTTAAGTATT | 286053 |
rs547613191 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285988 | GTACCTTGGAATCCC[A/G]TTTTTACAGCCTCCA | 286053 |
rs547640637 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328582 | AGTTCTCTCATGAGA[A/G]CCCAACTCAGGGATT | 286053 |
rs547645350 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287425 | TTCATGCCTGCTGCT[A/G]CTGTTCCTTTCCACA | 286053 |
rs547648706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197143 | ATTCTCCCATTCTGT[A/G]GGTTGCCTGTTCACT | 286053 |
rs547685832 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325685 | AGTTGGGTGCAGTGG[C/T]TCACACCTGTAATCC | 286053 |
rs547699800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286648 | CCATCATACACATAC[A/G]TATATTTAAATTAAG | 286053 |
rs547704536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145732 | CAGAAGTAATTCTGC[A/C]ACATGAAGCCTTCCA | 286053 |
rs547714987 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300089 | CTCCCAAAATGCTGG[G/T]ATTACAGGCATGAGC | 286053 |
rs547716397 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217718 | TAGGCTGGTTTGTGT[C/G]ACTGTCACTGTGCTC | 286053 |
rs547717042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096355 | CTGTCACAAGTGTTT[G/T]GTCCTTACCTGCCCT | 286053 |
rs547738148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098281 | AGGACTTGTTAAAAC[A/G]TAGATTGTTGGGGCC | 286053 |
rs547740858 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089988 | TATACTTTTACTGAA[A/G]TGAACTCACTGCTTG | 286053 |
rs547776327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233979 | CAGGAGATCGAGACC[A/G]TCCTGGCTAACATGG | 286053 |
rs547806411 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133374 | AGACTGAAATAATCC[A/T]GGGGTGTAAAATGGG | 286053 |
rs547837759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241806 | AGTAATTGAATTTAT[G/T]CCTTCCACAAATATT | 286053 |
rs547843483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147436 | CAAATGGATTAAAAT[C/G]TCTTTGGTGAAAGGA | 286053 |
rs547843582 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275052 | ATAGAATAATATCCT[A/G]GGTGGCTTCAGCACC | 286053 |
rs547861796 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323090 | ATATGAAATACCTAT[C/T]GATGTATCTGACTAA | 286053 |
rs547872295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191187 | ATTATGTGCATTATT[A/G]TTTCTTTCTTTCAGC | 286053 |
rs547879351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331684 | CCTTCAAAATCAGAC[C/T]ACATTGTTAGAAGTT | 286053 |
rs547892014 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249250 | TATACTGTTTCGAAC[A/T]TGGTTCTGAATTTTA | 286053 |
rs547913954 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284516 | GACCTTTCCCCTACC[C/G]TAAGATACTTAGACT | 286053 |
rs547916452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294447 | GTTCCAATTGCTCCG[C/T]GTCCTCACCAGCACA | 286053 |
rs547919833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365413 | TCTCTCCTGCACCCT[G/T]CAGGATCCCCCATGC | 286053 |
rs547920516 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287908 | TTTTGACTACTCGAC[A/G]CTCCCAGATACTCAT | 286053 |
rs547942629 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137475 | TAAGGCAGTTGCTAT[A/C]CACATGCAAGCTAAA | 286053 |
rs547951412 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270413 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 286053 |
rs547954902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300632 | GATGCGAAGAACATC[A/G]TCCCTGCACTGAAGT | 286053 |
rs547968100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103595 | TCTCCTCTCCTTCTG[C/T]GTGACTCACATTTCA | 286053 |
rs547974450 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260584 | TGGATCTAGGTGGCC[A/G]TCTTCTTTGTGGTTT | 286053 |
rs547986348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112640 | AAAATAAGCCAGTCA[A/C]AGAAAGATAAATAGT | 286053 |
rs547987461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203294 | CCTCATCTCCTGTCA[A/G]CCTGTTTGCCAGATT | 286053 |
rs547988733 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351921 | GGGAGACTGAGGCAC[A/G]AGAATCATTTGAACC | 286053 |
rs547992197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198512 | TTTGCGTGTGTTGAA[C/T]CAGCCTTGCATCCCA | 286053 |
rs548009890 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315292 | GGGCCTTAGGCTGTT[C/G]CTTTACCTCAAAGCC | 286053 |
rs548011379 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297129 | AACATCTCTGTCATA[A/G]TCACACACCCATTTT | 286053 |
rs548025137 | snp | C/G | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090654 | TCAAGAATAAGGCAT[C/G]ACATCCTTACACCAA | 286053 |
rs548030201 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212230 | TTAGCAAGGCGAACA[A/C]ATATTCATTTAAAGG | 286053 |
rs548034242 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238571 | CTTCATTAAACAGCA[-/T]TTTTTTTCCTTTCTT | 286053 |
rs548034534 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343982 | CTGCACACCAGCCTG[A/G]GGAACAGAGGGAGAC | 286053 |
rs548063210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248492 | ACCCCATCTCTACTA[A/G]AAATACAAAAATTAG | 286053 |
rs548069411 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144794 | TCATGAATTTTAAGT[A/T]GAATTTGATTATAAC | 286053 |
rs548070546 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108404 | TAGATGAAAGACTTG[C/T]AGAAGGCTGATACTA | 286053 |
rs548070703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177497 | TTAACCCCTTTTCTC[A/C]TCTCAACACAGTGTA | 286053 |
rs548092030 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293664 | TGAGACTTTTGAAGA[C/G]CATCCTGTAGGTCTT | 286053 |
rs548119589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250222 | CTAGAACTCCTGACC[C/T]TGGGTGATCCGCCTG | 286053 |
rs548124610 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217569 | GACAGGGTTTCACTG[G/T]GTTAGCCAGGATGGT | 286053 |
rs548140961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344572 | ACATGGTGAAACCCC[A/G]TCTCTACCAAAAATA | 286053 |
rs548141793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199127 | AATTTTGTTGATCTT[C/T]TCAAAAAACCTGGAT | 286053 |
rs548145927 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290157 | ATTTTTCATGACGTT[-/A]AAAAAAAACTCCACT | 286053 |
rs548146178 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295161 | CTTGTTTCCAGTAAA[A/T]GCACTGTGATTTTTA | 286053 |
rs548160639 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361287 | TGTCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 286053 |
rs548180677 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169667 | CACTGGCTGCACACA[A/G]TTGCTGTCTTCTCCT | 286053 |
rs548188655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263770 | AAAACAAAAAAAAAA[A/G]GAAGAGGCCTGATAT | 286053 |
rs548217976 | in-del | -/AAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239666 | GTTATGTGCTGATAC[-/AAA]AAAAAATTACAAATT | 286053 |
rs548237980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352589 | CATTGATTTATTAAA[C/T]TCCTGCATCACTTTG | 286053 |
rs548239069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127711 | GTTTGGAGTCTTGGC[C/T]GAAACTTAATAATAC | 286053 |
rs548244126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172583 | AGCTTGAAGTCCAAG[A/G]TATCTGAGCTGAGCT | 286053 |
rs548250746 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094450 | TCAATCTCAGTCTTA[A/C]TCTTTTCCCTACTCC | 286053 |
rs548259846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289152 | AGTACCTAAAACTTA[C/T]CACATCCTCAATAAA | 286053 |
rs548266742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220976 | CTAAAAATATCTCGA[A/G]GGTATTTTTTATGTT | 286053 |
rs548276571 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355871 | GTTGGGGGCCAATGG[A/G]ATGTAACTCAAAGAA | 286053 |
rs548289464 | snp | C/T | 0.000275976 | 0.0117436 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156017 | AGGTGTGGTGGCGCA[C/T]GCCTGTAGTTCCAGC | 286053 |
rs548299465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121142 | ATAAGTGAGGAGAAA[G/T]AAATGTTAGTTGGAA | 286053 |
rs548308842 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354123 | TTTTAGTAGAGAAGG[G/T]GTTTCACCATGTTGG | 286053 |
rs548312144 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315472 | CTTGCGTGTCAAAAC[A/C]TCAGTTTTCTCATTT | 286053 |
rs548317090 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251769 | TTTTAAATAAAGAAG[C/T]AGGCTTTTAAAGCAA | 286053 |
rs548320999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170578 | ATGCCCGACTAACTT[C/T]TGTGTTTTTAGAAGT | 286053 |
rs548321426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317072 | GGATTCCAGGCTGGC[C/T]CACCACTCCTGGCCT | 286053 |
rs548322125 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288790 | CCAGTCTTTATTTTT[A/T]AAATTTATTTATTTT | 286053 |
rs548323361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257658 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 286053 |
rs548343586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236474 | CATTTTACATAATAA[G/T]TATATAAATTTATGT | 286053 |
rs548354259 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300305 | TCACCTCCACCTCCT[-/G]AGTACCTGGGACTAT | 286053 |
rs548389163 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358973 | GAGTTAACAGTTGAA[A/G]TGTCAGATTTCGGCC | 286053 |
rs548406031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226852 | TTTCTGCTTTCTCCC[C/T]TAGTTTCCTCTTTTC | 286053 |
rs548426536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353191 | CATCCAGCAGATTTT[C/G]TGGTGAATTCTCTGG | 286053 |
rs548427642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360619 | CATGGGAACTTGTGG[G/T]CGGGGTGGGCAGGGT | 286053 |
rs548452405 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140426 | CCAGCACTTTGGGAG[C/G]CCAAGGCGGGAGAAT | 286053 |
rs548462196 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092345 | TTATGGCATTCTGTA[A/G]GTGACCGAGAAATGA | 286053 |
rs548479253 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264992 | AGGGTGAGAGTCCTC[A/C]CCTCAGGCACAAAAC | 286053 |
rs548482690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263047 | AGGGACCTCATAATG[A/C]GGTAGCTGGGGGAAT | 286053 |
rs548491288 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135562 | ACTGAAGTTTTGTAT[A/G]TGGAATAAGGTACGA | 286053 |
rs548527589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180723 | TTATTTGTGAAACTG[C/G]GGGGAGGAGATCAAG | 286053 |
rs548534878 | in-del | -/AAAAATACAA | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257122 | AGCCCCATCTCTACT[-/AAAAATACAA]AAATTAGTCAGGCGT | 286053 |
rs548540678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262522 | CCATTTATTAGTATT[C/T]ATCCATTTATTGTTC | 286053 |
rs548570681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310457 | TCAATTGTAGCTATT[A/G]CAATTATGTAAAAGA | 286053 |
rs548585264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205785 | AAATGGTTAGAATTA[C/T]AGGTTGTAAATACCA | 286053 |
rs548589547 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365061 | GCCGTGGCTTGTTTC[C/T]ACCCCTTTGTGGGTG | 286053 |
rs548590222 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181334 | GCCCGTTGAGAGGAA[A/G]GTTTGTTGTGAAGGA | 286053 |
rs548597198 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228467 | CAAGCTGGGTGCTGA[A/G]AAAACACAAAAGGAA | 286053 |
rs548598031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193582 | TTTCTATAAAGAGTC[C/T]ATATAGTTTTATAAT | 286053 |
rs548598543 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359083 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGACTC | 286053 |
rs548600910 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202174 | CCTTGCGCTTCCTTC[A/G]TGAGGCAATGCCCCG | 286053 |
rs548633196 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142661 | CCATGCTGGAGGACA[A/G]TGGTGCTATCTTGGC | 286053 |
rs548654463 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227836 | TTTTTTTTCTGTAAA[C/T]TATATATTCGCAAAA | 286053 |
rs548661705 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171879 | GCTCTGTCCAGAGTG[A/G]TGTGGTAGTCACTAG | 286053 |
rs548662924 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266568 | TGTTTTATACAATGT[A/G]TTATCAATTTGTCCT | 286053 |
rs548693841 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223872 | GCTGGAGTATAGTGG[C/T]GCAATCATAGCTCCA | 286053 |
rs548695712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278439 | CTAGTGCAGAGGAAG[A/C]GAAGGCAAGCCATTG | 286053 |
rs548707335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165098 | AGCCTCCTCCTTGTT[C/T]CTCCCTGGCCTAACA | 286053 |
rs548720444 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252122 | GTATAGTCAGCAAAA[A/C]GAGGATAGCACCAAT | 286053 |
rs548759567 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186455 | CAAGTACATTCAGAA[C/T]ACTTTGAGGATTCAC | 286053 |
rs548763719 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342190 | GTTCTACTTGTGCTC[A/G]CTCGTAATTGTCACC | 286053 |
rs548772598 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151428 | ATTTGGAAGTCTCAT[A/G]AAATTGGAATCCTAA | 286053 |
rs548775523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144215 | GGATTCTCTCCAGTG[A/C]ATGCCTTAGGCTACA | 286053 |
rs548777779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272153 | CGAGTAGCTGGGACT[A/G]CAGGCGCCCACCATC | 286053 |
rs548789070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282869 | AGTTCTGGACTCCAC[C/T]TGAAAATATTTTTAC | 286053 |
rs548793987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318830 | AGGCCATAGTACAGG[A/G]AAGGGGAACCTAGGC | 286053 |
rs548800043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188268 | TCTACTCAAAACCAC[A/G]GTGTAGTTGCACAAG | 286053 |
rs548814036 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101258 | TAATGGAGAAACTAC[-/A]ATAGTAGTTCAGCTG | 286053 |
rs548818820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284012 | CAAAAAAATTAGCTG[A/G]GCGTGGTGGCGGGCG | 286053 |
rs548838793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137300 | ATCTTATAATCTAAT[C/G]AACTTCTTGTCAGAT | 286053 |
rs548842612 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091832 | TGTGACCACTCGCCG[A/G]CGACGGCTGATGACG | 286053 |
rs548852864 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316769 | TCCTTCCTTCCTTCC[C/T]TCTCTCTCTCTCTTT | 286053 |
rs548870370 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336578 | ATATGGGTGGCTTTG[C/T]TGGGTGATACTGCTG | 286053 |
rs548880328 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283681 | CACATAAAGCAATGC[A/G]CAAATGAAAGGTATT | 286053 |
rs548889532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276517 | CACTGATTGTAGAAT[A/G]ATTAATAATGGAATA | 286053 |
rs548892905 | in-del | -/T | 0.411746 | 0.190626 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096634 | TACTGTGTGGAATCC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs548914336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318297 | GTCCCAGCTACTTAG[A/T]AGGGCTGAGGTGGGA | 286053 |
rs548917779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094845 | CTGGCGTCTCTTCCT[C/T]TTCTTTTCTTTTCTC | 286053 |
rs548919547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102901 | CCAGCAAAGGAAGGC[C/T]TCAACAAAAATGAGA | 286053 |
rs548929909 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335255 | GGGTTAAGGAAATCA[C/T]TGCCACCATTTTTAA | 286053 |
rs548935938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196391 | GTGGTGTGTGATGTT[C/G]CCCGCCCTGTGTCCA | 286053 |
rs548954201 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205731 | GATTGAAGCAGGGGA[A/G]TGGGGGAGGAGGACC | 286053 |
rs548968161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230649 | CTATTGTAAGCTAAT[C/T]GTATGCCAATGAGGA | 286053 |
rs548972343 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327122 | ATAAAAAAAAATTAG[C/G]CGGCGTGGTGGCGAG | 286053 |
rs548997027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125130100 | TTAGTTGGTTTCGCT[C/T]TTTTTTTTCTTGTAA | 286053 |
rs548998514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245596 | ACACAGCAATGCAAG[A/G]AAAAATCTAAAAAAA | 286053 |
rs549004886 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141703 | CTCTAATGTAGTCTC[-/TG]TGGAGAGGAGTGAGG | 286053 |
rs549005597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095399 | TTTGAGACCAGCTTG[A/G]GCAACACAGGGAGAT | 286053 |
rs549020822 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290363 | TAAGGAAAAAGGGGT[G/T]TCTCATGGGAAAAGG | 286053 |
rs549023298 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144735 | TGCTTTCATTCTTTC[A/C]TACTTGTTTGTGCCT | 286053 |
rs549027661 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238107 | CTCATCTCACTATCA[A/G]CATTGATCCTGGCAT | 286053 |
rs549040560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328533 | CACCAAGGCCTGCTG[G/T]TTTCAGAATTCGCTG | 286053 |
rs549043239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341413 | TCCTCTGTTTTGTCC[C/T]GCTTACAACTGCAGG | 286053 |
rs549046265 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149499 | ATGTGATGAAAGAAA[C/G]CTTTATTTTCTTTTC | 286053 |
rs549049703 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210013 | GCATTTGTTCTTTCA[A/G]GGTCTCTACAGAATA | 286053 |
rs549052195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363120 | GTTGCATTTCAATGT[A/C]ATGGAAGCCAAAGTT | 286053 |
rs549062078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172542 | CCCAAAAGGGGGAAT[A/G]ATACATCTTACCAGG | 286053 |
rs549064759 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336136 | GCTTTGAAGATAGGA[A/T]GGACAGAGCATTGAG | 286053 |
rs549067403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247096 | ACTTTGGGAGGCTGA[A/G]TGGGGCAGGATTGCT | 286053 |
rs549067866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222040 | TCTTTCTTTTTATTT[A/T]TATGTATACTCATTT | 286053 |
rs549073071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202088 | GCACAGTATTTTGGC[G/T]AGAGTGTCCTGTTTT | 286053 |
rs549078425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093883 | CTCACTGCAGCCTTG[A/G]ACTCCTGGACCCAAG | 286053 |
rs549085877 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302248 | AGGCATGAGCCACCA[C/T]GCCAGGTCCCAATTT | 286053 |
rs549088088 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292110 | ACCACACCTACCTAC[A/T]AGGAGGGCTGGACAA | 286053 |
rs549128398 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304896 | CTGAAAAAAAAAAAA[A/G]AGAGAGAAAGAAAGG | 286053 |
rs549130502 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151358 | AAAATCAAAATTCTT[C/T]TCTAATCTTTAATGT | 286053 |
rs549135518 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191818 | TCTTTACAACATCCA[C/T]ACGCAGGAAAGGAAT | 286053 |
rs549135554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194329 | TTTTCCAGAATGTTG[G/T]ATAGGTAGAATTGTA | 286053 |
rs549150584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208072 | TCCAGCTCATATTCA[C/T]TTGTTCATTTTGAAT | 286053 |
rs549152378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100510 | CAGGTTTATGTTTTA[C/T]CTCTGTCTCTCCTAC | 286053 |
rs549159047 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335271 | TGCCACCATTTTTAA[A/T]CAGCGATTATGTGCC | 286053 |
rs549174561 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201039 | CATTTAAGGTCTTCT[C/G]TATACTGTTTATTCT | 286053 |
rs549189671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303517 | TATAAATTAACTGCT[C/T]ATTTTGTGCGAAGTA | 286053 |
rs549191392 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118792 | TATACCTCTCACCTT[A/T]GCTGCTCTCCTTTTC | 286053 |
rs549209917 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201832 | AGTAGCCCTTGATGA[A/G]CTGTGGTGGGCTCCC | 286053 |
rs549223646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340820 | ATCTCTCCCTCACAA[G/T]GTCTTTCCAACAATT | 286053 |
rs549226973 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286069 | ACCCTCCAGTGCCTG[A/G]GAGAGTTAATTTGCA | 286053 |
rs549228265 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341080 | CAGTCACCTCTCCAT[A/T]TTTTTTTTTCTTTTG | 286053 |
rs549254939 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121706 | TAATAATAGCCAACT[G/T]GTGATGCTTTTTGTG | 286053 |
rs549260142 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307320 | AAGCATGGTGTATGG[A/C]GAGATGCCTAGTATA | 286053 |
rs549267155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305524 | GAAGGCAGCTGGAAA[A/G]TCAGACCTGTAGCTC | 286053 |
rs549279686 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276034 | CAGAGGTCTGCCCCC[C/G/T]GCACTGGGTCTTCTG | 286053 |
rs549299421 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159788 | AACATGGTAAAACCC[C/T]GTCTCTACTAAAAAT | 286053 |
rs549309609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200557 | CGCTGTTAGTCTGAT[A/G]GGCTTCCCTTTGTGG | 286053 |
rs549316812 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160294 | AAGGTTGCCTAGAAC[A/G]TTCTGTAAAGAACTC | 286053 |
rs549323135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265810 | GAACATCTATTGATC[C/G]TTAGTTGTTTTTTAA | 286053 |
rs549334674 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134868 | GAGTAGTTGGGACTA[C/T]AGGCGTATGCCACCA | 286053 |
rs549339245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311937 | GCCAGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 286053 |
rs549359704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108902 | TGGCCTATAATGTGA[C/T]GCTTTGCCAAGGAGT | 286053 |
rs549369419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154375 | AACTTACCAACAATC[C/T]CTGGGAAGTCCCTTT | 286053 |
rs549378833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246432 | TGTGATCCACCCGCC[G/T]CCTCCTCCCAAAGTG | 286053 |
rs549383255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358120 | GGCAGATCACCTGAG[A/G]TCAGGAGTTCAAGAC | 286053 |
rs549389981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146030 | AATAATTTTCTTTTT[G/T]TTATCAGATTTCTTA | 286053 |
rs549397067 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299631 | GTGGGGACACAAAGC[C/G]AAACCATATTAAGCA | 286053 |
rs549401290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291460 | TTATATAACAGTTCT[A/G]TGAGCTGGTCAATGA | 286053 |
rs549426179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124840 | TACTCTTTTGCCCAG[C/G]CTGGGGTGCAGTGGT | 286053 |
rs549432704 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215504 | CTGCAATAAACATAC[A/G]TGTGCATGGGTCTTT | 286053 |
rs549446585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129602 | TTTCATTGATATTCT[C/G]AATACTGAGAGCAAA | 286053 |
rs549452646 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255161 | CTGTATGAATGAGCC[A/G]TCTTGGAGGTGGATT | 286053 |
rs549455379 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119586 | GACTAGCACTTTATT[A/G]TATCTCTTTGATCAT | 286053 |
rs549457119 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167393 | AAGTCAAGGCCCGGC[A/C/G]TGGTGGTTTATGCCT | 286053 |
rs549491541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352018 | GACTCCATTTCAAAA[A/C]TATATATACATAGTG | 286053 |
rs549522462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261053 | ATTCTGAGAAAAGAA[A/G]CCTCGATATTTACAT | 286053 |
rs549527542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145109 | CTTCAGTGATAATCA[C/T]TCTTTGTTTTTCCAG | 286053 |
rs549529305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153251 | ACTTTTCAGCCCTAA[A/C]CTCACACTAGAATAG | 286053 |
rs549532236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233084 | TAAGGAATCTGAAGC[A/G]TGGCAGATCACTTTG | 286053 |
rs549537180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103708 | ATTTGAATAATTTCT[A/G]TTGCTAAGTTCATTC | 286053 |
rs549542175 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220868 | TTGGAATTTGAGTTG[C/T]TGCCAAGTCTTGTGT | 286053 |
rs549553625 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216657 | AAAAAAAAATGGTCT[A/G]TGGGTTTTGGGCAAA | 286053 |
rs549577367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329197 | TCAGTCCCCAGCAGC[A/G]GGCAATCCTTCCTTA | 286053 |
rs549585684 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223609 | CAATGTACCAGGGTT[A/G]CCTTTTCTCCACATC | 286053 |
rs549599399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208837 | GGTAATTATCTAATT[A/C]GAGTCTTTTCAAGTG | 286053 |
rs549609615 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106662 | TGCACTCCAGCCTGG[A/G]CGACAGAGCAAGACT | 286053 |
rs549611542 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214532 | GTTTGCCACAGACCA[A/C]CCCCTTTTGCCTCTG | 286053 |
rs549612723 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187684 | AGCAAAGGCAGAAAT[G/T]GAGGGCAGTTGTCAA | 286053 |
rs549622423 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246969 | ATCTCCAGTATACTA[C/T]ATAATATTGTTAACT | 286053 |
rs549631084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210187 | AGTTTACCCACTTCA[A/G]AGGATTGTTGTGGAG | 286053 |
rs549651636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161869 | TTGATTTCCAGACAT[G/T]CTGACTTGCTTGCTT | 286053 |
rs549659908 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321121 | CCCCACCTCCAGTAT[C/T]GGTGATTACATTTCA | 286053 |
rs549673031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115590 | ACCCCATCTCTGCCA[A/C]AAATACAAAAATTAG | 286053 |
rs549684707 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260253 | TACCTGGAAGAATCT[A/C]GTTCCTTAGGCTAAG | 286053 |
rs549730272 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217365 | TATTTATTTATTTTT[A/T]ATTTATTTATTTTGA | 286053 |
rs549730898 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345346 | ATCAGTAATTAACTC[A/C]AGGACCAAATTGTCT | 286053 |
rs549732373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210800 | CTCACTGCTCACTGC[A/G]ACCTCCACCTCTGGG | 286053 |
rs549745439 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259436 | CCCTATTGGTTGTGC[A/C]CTCCTTATGAAAATC | 286053 |
rs549754701 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162726 | CTTTCTCTTACCACA[A/G]AAACACCTACCACAG | 286053 |
rs549755416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275185 | CATATCCTTTTCCTG[C/T]CCATAGGAGAATGTC | 286053 |
rs549760621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267804 | CGGTACTTTATCTAA[C/T]AGGTCATGTTGAATT | 286053 |
rs549761976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300163 | GTCACTTCAAGGGCT[A/G]TGCCTCTTTTTTTTT | 286053 |
rs549762627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138710 | GTCAACTCGGTCAAA[A/G]GAATTTGATGATTGT | 286053 |
rs549773153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314213 | GCTTATGCAAATCCC[A/G]TAAATCAGTAATGTG | 286053 |
rs549778941 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267188 | AATTTTTGTATTTTT[A/T]GTAGAGACAGGGTTT | 286053 |
rs549786494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178348 | ACTGGATGAGTAAGC[A/G]GGTGGTACAGAAAAA | 286053 |
rs549787252 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183917 | GAACTATTCTATTTG[C/G]TGCTTAGTGAAAATA | 286053 |
rs549789994 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244676 | CAAAAGTATTATACT[A/G]TGCAACTTTATTATT | 286053 |
rs549797552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111589 | CGGATCACTTGAGGT[C/T]AGGAGTTCCAGATCA | 286053 |
rs549845385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203339 | ACCCATGGACCTTGC[A/G]TAACTAATATCTAGA | 286053 |
rs549849329 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269621 | TCATAGCTTTCTACA[A/C]GATCATTAAGATCCT | 286053 |
rs549850184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364657 | ATATGCAAGATAGAA[A/G]TAGATCCAGAACTTT | 286053 |
rs549855709 | in-del | -/TGTA | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183661 | GTGTGTGTGTGTGTG[-/TGTA]TATAGTATCTGGCAC | 286053 |
rs549883022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366169 | CTGCTTTGTTGCCCT[C/T]ATAGCCCATAAGGTG | 286053 |
rs549888363 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298573 | CTTAAACCATCTCCA[-/C]CTTTTGTTTCCTTAT | 286053 |
rs549904454 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300894 | ATGGAAGAACATTCC[A/G]CCTGGGCTCTGTAGC | 286053 |
rs549905961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183130 | ACACACATGGAGCAG[C/G]AGTGTTGTATGATAT | 286053 |
rs549916341 | in-del | -/ACGTGT | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272826 | CGTATATATATACAC[-/ACGTGT]ATATATATACACACG | 286053 |
rs549923211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249082 | AAGCTGAGGAACAAG[A/G]ATCTTTTGAACCAGA | 286053 |
rs549932162 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109723 | TCCTAATTCCTATAC[C/T]AGGTGTTTGTCCCTG | 286053 |
rs549946621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132105 | CTTCTTCTTCTTATG[A/G]GGAGTTGGTGGGTAC | 286053 |
rs549947556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169445 | GTGTCCCACAGTGAC[A/G]TTTTCCCCATGATTT | 286053 |
rs549955933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148284 | GCCCATTTCCTCCTT[C/T]GCAGGAAGGTCTCTT | 286053 |
rs549958697 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133537 | TTGAGCTCAGGAGTT[C/T]GAGATCAGCCTGGCC | 286053 |
rs549961186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319968 | ATCACCTGAGGTCAG[A/G]AGTTCCAGACCAGCC | 286053 |
rs549975680 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240722 | AATGGTTATTTTTTT[G/T]TTGTTAGTTTGTAAT | 286053 |
rs549978781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262618 | CTTACTATGTGCCAG[A/G]CACTTTGAAATTTGG | 286053 |
rs549989862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280089 | AGGACTCACTGCCAA[C/G]AAAGTGATGATTTTC | 286053 |
rs550017736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308409 | TGGTCTTCTTGAGTC[A/G]GAGAAGTCTTTTTCC | 286053 |
rs550072647 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214195 | CCAGGTTGGTAGGCA[A/G]AATTAGGGAACTGTA | 286053 |
rs550088612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147612 | ATATGTAGGATTTAA[C/T]TTGGTATATATTCTC | 286053 |
rs550098302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140445 | AGGCGGGAGAATTAC[C/T]TGAGGTCAGGAGTTT | 286053 |
rs550125172 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332405 | TGAAATATACCTGGG[C/T]TTGGCTAGCTCTGTG | 286053 |
rs550126328 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272975 | CCAAGAGGGAGCTGG[A/G]TGACACGGGGCAGGA | 286053 |
rs550133354 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285062 | TGAATTAGAGGCAAA[G/T]GTACTTTCATGCTGT | 286053 |
rs550169167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226914 | CTTGTTCTGGCAACC[C/T]TCTGCCTCATCTTTT | 286053 |
rs550173347 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323896 | AATGTTATTTTCAAA[C/T]CACAAATCTGATAAA | 286053 |
rs550182882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234760 | TTTCAATCATCTCTC[G/T]CAATGTAAACTTGGA | 286053 |
rs550210553 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318606 | AAAACTAGAAGCAAA[C/T]CTTAAGCTTCTGATC | 286053 |
rs550242157 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112559 | AATATTATTCAGTCT[C/T]AAAAAAAAAATGAAA | 286053 |
rs550246525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185030 | TTCTTTTATGAAAAT[A/G]ACCACCATGTCTTCA | 286053 |
rs550257545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099585 | AGAAAGTGCATCAGG[A/T]AGGGAGTGATTAACT | 286053 |
rs550259864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325420 | CAGTGGCACGATCTC[A/G]GCTCATTGCAACCTC | 286053 |
rs550260446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316114 | ACCTGGTCTAAACCT[C/T]ATTCTTATCAATGCA | 286053 |
rs550270808 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238281 | CATTTCCATCTGTCT[C/G]TCTTTCCTCACAACA | 286053 |
rs550288333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366554 | TTAGCTCATGATAAG[A/G]CAGGCACTACTCACA | 286053 |
rs550305474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227509 | ATTAAGGACAACTTT[C/T]ATTAGCATCTTTGTC | 286053 |
rs550324581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243555 | TTGAAAATTGAGGAG[A/T]GATTGTGTTGATAAA | 286053 |
rs550327367 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167820 | AATGCAAGCATTGGG[A/G]GAAGTTTTCTCAGTT | 286053 |
rs550346031 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264664 | TCAGGGTGGGCTGTT[C/G]TTGAAGCTACTTCAG | 286053 |
rs550346911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288844 | GTCTCGCCCTAGCTG[G/T]AGTGCAGTGGCTCGA | 286053 |
rs550361191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283507 | TCTGGGCAAGTGAGA[A/C]CTTGTGTCAAAAAAA | 286053 |
rs550366816 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198400 | TTTTTAGCATGAAAG[C/G]CTGTTGAATTTTGTC | 286053 |
rs550381639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333014 | GTGGAACACTGAGCT[A/G]TGAACCCAGTATCAT | 286053 |
rs550390276 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206119 | TAAATGTTAAAGCAG[-/T]TATAAATATTTATAT | 286053 |
rs550416728 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155106 | TCACCTCAGGATATG[C/G/T]GAAGTCCAGAACAGA | 286053 |
rs550445018 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345053 | AAAAAAACCTCCACA[G/T]TTTTGACAGCCGATT | 286053 |
rs550446110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171276 | ACAAGGGCAGGAACT[A/G]GTTCTCTTGACTGCT | 286053 |
rs550464781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302886 | TAGGAAGTTGGTGCC[C/T]GTGCCTCCAAACAAC | 286053 |
rs550464957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295261 | CCTAATCTGGTGACC[G/T]TTGTGTTTCTGTCAA | 286053 |
rs550487938 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235090 | ACCTCTACTAAAAAT[A/G]CAAAAATTGGTGTGT | 286053 |
rs550507516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243963 | AAGCAAAATTTATAA[A/G]GACATTCTGGAGCCA | 286053 |
rs550524216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115463 | ATGTTTCTATTAAAT[A/C]TTTCAGGCCGGGCTC | 286053 |
rs550529700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289233 | AAAAGCATTGGAAAC[A/G]GGAACTTTGGAGGAA | 286053 |
rs550547145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205587 | TTCCCCCATAACCCT[A/G]CTTCAAAAACTAGAA | 286053 |
rs550557498 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211758 | GTAGGTTATTAAACC[G/T]TTTGGTCTCTGCCAC | 286053 |
rs550579389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348255 | TATACAAAATAAGTA[A/C]CATATTGGATCCTTA | 286053 |
rs550583045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341561 | GGTTTTTGTTACTGC[A/G]TTGATTCATCTGTTA | 286053 |
rs550588764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142674 | CAGTGGTGCTATCTT[A/G]GCTCACCACAACCTC | 286053 |
rs550590142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338846 | TTCTTGACAAGGACC[A/G]AATTAGGCTATCATG | 286053 |
rs550592471 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101945 | TAAACTATTTTATTA[A/G]TATTTTTTTCTCTTT | 286053 |
rs550605711 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304810 | TGAGAATCGCTTGAA[C/T]CCTGGAGGCAGAGGT | 286053 |
rs550607087 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326977 | AAAAAAGAGAGAGAG[A/G]GAGGGCCAGGCGAGG | 286053 |
rs550619908 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250915 | GATTATAACATTAGT[A/G]TTAACCTACATTCAC | 286053 |
rs550626961 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346729 | ATTGGTTTGAAGTGG[A/T]TATTGTATGACCAAA | 286053 |
rs550642671 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252199 | ATGAGACTGGAAAGG[A/G]ATGACAGAAAGAAGA | 286053 |
rs550644086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236528 | GGGAATGGAAATGTT[G/T]GCATATGTGTGTTTC | 286053 |
rs550650595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276571 | TAAAGGCAGACGCAT[A/G]TGGTTATTATATCTG | 286053 |
rs550661256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114625 | GGATGCGGGGAGCAT[A/G]TGTGCCCTGGCCTCT | 286053 |
rs550664184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098858 | GTTTTAAGTTCTGGA[A/G]TGATCTTGCCAATGG | 286053 |
rs550665341 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164833 | CTTACCATAATAATA[G/T]CAAGCCTAGCTAACA | 286053 |
rs550668596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282954 | TTGTAGGAAGGTAGT[C/T]TAGCATAATTGTTGA | 286053 |
rs550679661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207132 | AGTAAGATTATGGGG[A/G]CAGAGGGATGGAATT | 286053 |
rs550692789 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348844 | TCTTTATTAGCAGCA[C/T]GAGAACGGACTAATA | 286053 |
rs550702176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159147 | TTTGAGAGCAAGAAA[C/G]ATTATATTCACATAA | 286053 |
rs550724128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108013 | TACTCCAGCCTGGGC[A/G]ACAGGGCCAGAGCCT | 286053 |
rs550725570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142144 | AGTTATCTATTCTGT[A/G]ATAATGATAATGACA | 286053 |
rs550732782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220304 | TGGAGTTGCCTAACA[A/G]TATAATTTCAAATGA | 286053 |
rs550733446 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204881 | AACTAGATCCGGCCA[C/G]TTTCTACCAGAATGA | 286053 |
rs550737079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121168 | TGGAAAAGCTATATA[C/T]ACATGGTGAGAAGTT | 286053 |
rs550738595 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197272 | CATGAAGTCCTTGCC[C/T]ATGCCTATGTCCTGA | 286053 |
rs550759847 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263205 | CTGTCTTCAAGCAGC[C/G]TAGACTTGGATTTGA | 286053 |
rs550782624 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112736 | GGTTACCAAGGGATT[G/T]GGGAAGGGAAGGGTG | 286053 |
rs550802355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121774 | CATTTAATCCTTACA[C/G]AAATACTGTCAGGTA | 286053 |
rs550807469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353472 | AGTCTAACTCTTGCA[C/T]TATGAATACCAAAGA | 286053 |
rs550837204 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093165 | CGGGGCCTGTTTCCT[A/G]GTTCATAGGTGGCTT | 286053 |
rs550841887 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347297 | ATGTTCCTAAATACT[A/G]TAATCCTCATTGTCT | 286053 |
rs550879636 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361700 | AAGCTCTTTTGGGAG[C/T]GAAGAGCGCTAAACA | 286053 |
rs550882231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250275 | CGCCCAGCAACACTA[C/T]TTTATATGTATTATT | 286053 |
rs550899251 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164328 | GAACCTCAGTGTTTT[C/G]ACATGTAATTCAAGG | 286053 |
rs550905438 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238929 | TGTATATTGTTACAG[A/G]GCTGTTCTTGTATAT | 286053 |
rs550915856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107087 | AGTTGCACAGGCTCA[C/T]TTTCTTCATTTTTGA | 286053 |
rs550922947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174077 | TGAGCACTGTTAAAA[A/G]GATTGCCTGTGAAAT | 286053 |
rs550926195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237337 | AAACACACTCACACA[A/G]TCTCCATCAGAATAG | 286053 |
rs550942937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362252 | CAGAGGAGGCATGCC[G/T]TGATTCAGCACTGTG | 286053 |
rs550943598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256921 | AAGCAAGACTCTGTG[A/T]CAAAAAAAAAAAAAA | 286053 |
rs550956340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151045 | TTGAGGAGGTTTTTT[A/T]AAAAAGATGTAATAG | 286053 |
rs550958825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257934 | AGAGAAGAACACAGG[A/G]GCATGAGAGGGTGGT | 286053 |
rs550962130 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235308 | TTCCTGCATTTTTTT[-/C]TTCTTGATTTCCATT | 286053 |
rs550972435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200594 | TGACTTTTCTCTCTG[C/G]CTGCCCTTAACATTT | 286053 |
rs550976668 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257055 | TTGGGAAACCTAAGC[A/G]GGCAGATCACTTGAG | 286053 |
rs550986285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167548 | GCTGAGGCACGAGAA[C/T]CACTTGAACCCAGGA | 286053 |
rs550989777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187539 | CAGTTTTAACATCAG[A/G]AGAACTTAATTAGAA | 286053 |
rs550998902 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152705 | AGAACGTTATGTTGA[-/T]TTTTTTTTCCCTATT | 286053 |
rs551001715 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100685 | TCCTGCCCAGCTTCC[C/T]GAGTAGCTGGGATTA | 286053 |
rs551008297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136206 | TTTGATAAACAGGAG[A/G]GTAACACCAGACTTG | 286053 |
rs551011636 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290437 | CAGACCATAAAATCT[C/T]TCATCTCTACTTCTT | 286053 |
rs551012281 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227423 | ACCAGGGCCTTCCCC[C/T]CCAGAGCCACTGCTT | 286053 |
rs551017122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138067 | AATTCAGAAAGACTT[C/T]CTTTTTACCTCCTGA | 286053 |
rs551017143 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281830 | AGCAATCCTCCCACT[G/T]CTGCCTCCCAAAGTG | 286053 |
rs551040992 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216300 | GTTTGAGTTTCTGCT[G/T]TCAGTTCTTTTTTGT | 286053 |
rs551042038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303664 | ATTCCAATTGCTGTA[C/G]AGAAATTCAACTCCA | 286053 |
rs551054349 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091464 | GAGCTGGATTACAGC[A/C]CCCGCCCCAGAAAGC | 286053 |
rs551060691 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309843 | ATTTCAGAGTATTGA[G/T]CAAGGCCTACACTGA | 286053 |
rs551080725 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165994 | AATAAACTGATGGAG[C/T]ATTAATAATTTCATA | 286053 |
rs551092365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272649 | TACTGCCACAATAAA[A/G]CAGTTATAGAAATTG | 286053 |
rs551093607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158498 | GACCTTTGAAGGGCC[A/G]GGCTGACCACAGCAC | 286053 |
rs551115676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297598 | TACTTTGGAAGGACC[A/G]GACAGAAAGATCAGT | 286053 |
rs551122715 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231651 | TATCATGCATAGGAA[A/G]AATACTGTTTCATGA | 286053 |
rs551128356 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317089 | ACCACTCCTGGCCTA[C/T]TGTTTCTGATTTCAC | 286053 |
rs551147195 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220226 | ATCTAAAACTATATA[G/T]ATGAGGATGGTTTTC | 286053 |
rs551154303 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364635 | TGGGTGCATGCCTGT[G/T]TGGGATATATGCAAG | 286053 |
rs551158270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172261 | CAGGCAAAGGACTGA[A/G]GTGGCATATCTGTAT | 286053 |
rs551169528 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095081 | TCTCGAACTCCTGGG[-/C]CTCAAGCCAACCTCC | 286053 |
rs551180423 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126721 | AACACAGCTCTGGCA[A/G]TTATTAGCATTGTGT | 286053 |
rs551186869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245719 | CTGGATTACTGAAAA[C/T]TGAAACAAAATTAAG | 286053 |
rs551191431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270545 | TTGAATTGCTTTAAA[C/T]AGAAGCAAGTTATGA | 286053 |
rs551198134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312660 | AAATAAATAAATGTG[C/T]TGCATCTGCAGTGCC | 286053 |
rs551227464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264355 | CTCTGTGGAGTCCCA[C/T]TCATGCCTGTCACTC | 286053 |
rs551251605 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334397 | ACATAAAGGTTATTC[A/T]CACAGCAACAGAACA | 286053 |
rs551253907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179232 | GATCTCTCCATCTCA[A/G]ATTTCTTTGAGGTAT | 286053 |
rs551261613 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306786 | ACTGTCTGGATTTGA[A/G]TTCTTGTTCCACCAA | 286053 |
rs551266201 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310575 | TAACTACATTTAAAT[C/T]CCCGGTTACTTTAAG | 286053 |
rs551270414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125127822 | ATGAGATACCTTGGG[A/G]ATGGGATCCAAGTCT | 286053 |
rs551275482 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144338 | CTGCTCTGGAATGAA[A/G]GTTTGATTGGTCTGT | 286053 |
rs551285529 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167720 | GTTTAGGCTAGACTT[-/G]GGGGGGAAAAATCAG | 286053 |
rs551289160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144234 | CCTTAGGCTACAGCT[A/G]TAGGGCAGCTGTGGT | 286053 |
rs551321087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188760 | GCGAACTAAGGCCAA[A/C]ATGTGCAGTTTGCTT | 286053 |
rs551326049 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109969 | GTTTTTGAGTTTATT[A/G]TGTACTTTTCTGCCA | 286053 |
rs551326121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190335 | ATCCCCATCTTCATG[A/G]TGAAGCAGCCTCAGA | 286053 |
rs551327689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232220 | ACAAAAAAATCAGCC[A/G]GATGTGGTGGTGCAT | 286053 |
rs551333829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363282 | CCAAGGCAGGTGGAT[C/T]ACTTGAGCTCAGGAG | 286053 |
rs551336888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272566 | ATGACATCATTTCCG[C/G]TAACAGACCAGTCAG | 286053 |
rs551341538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278489 | CAGAGCGTGTGCTTT[C/T]GTGAGGCATGAGGGA | 286053 |
rs551351533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151601 | CTTGTTTTTATTGTT[C/T]TATTTGCTTAAACAT | 286053 |
rs551363590 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193313 | TCACAAAACATGTAT[C/T]TTACAAAGAATATAG | 286053 |
rs551365210 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156554 | AGCAAGTAGGTGCTA[A/G]GTTGGTCCATTTGTA | 286053 |
rs551367363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222908 | TCCCTACAAAAGGAA[A/G]AGAAATAGCCAGGTG | 286053 |
rs551370240 | snp | A/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210650 | CTTTTTTTTCTCACC[A/G/T]ATCTGGCCTCAAGGG | 286053 |
rs551371667 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202072 | TAAGACCATGGGAAA[A/C]GCACAGTATTTTGGC | 286053 |
rs551380442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239106 | AGGATCCAGTTTTCA[C/T]CCCATTTGGCAAGGT | 286053 |
rs551384946 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122208 | AAATGCTGCCTATTA[C/T]ATGAAATGTACTATG | 286053 |
rs551387759 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215596 | GGTATTTCTAGTTCT[A/G]GATCCCTGAGGAATC | 286053 |
rs551389649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191060 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 286053 |
rs551425002 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170155 | AACTGTCTTCTCTTC[A/C]TTTTCACTTTATTTC | 286053 |
rs551426619 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159657 | TTTTAGGCATCTACT[A/G]GGGGTTTTGGAATGT | 286053 |
rs551427595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259652 | GAACAGCAACATCTT[A/G]CCCTGTGGCCTACTC | 286053 |
rs551430918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318934 | TAGAGAGATGCACAA[A/G]GAGAGAAATCTGGAG | 286053 |
rs551445685 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118124 | GGAGGCCGAGGCGGG[C/T]GGATCACCTGAGGTC | 286053 |
rs551448142 | snp | A/G | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090919 | TGAACCTGAAATCCT[A/G]GGAAAGGCAGGTGAA | 286053 |
rs551462888 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189466 | TGGGCCTGTCCAGAC[A/G]TGCCTAAATAAGCCA | 286053 |
rs551464674 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197111 | AGCCCTTTATCAGAT[A/G]GGTAGATTGCAAAAA | 286053 |
rs551466878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305017 | GGAAGGAAAGAAAGA[A/C]GGAAGGAAAGAAAGA | 286053 |
rs551488514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336265 | ATATTAAATAATCAA[C/T]TACTCAATTAAATTC | 286053 |
rs551495045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356226 | TCTCATTATGTATGT[C/T]TGTGTGTATGGGGGG | 286053 |
rs551527982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101904 | GGATAGTTTAACGAT[C/T]ACAGGTTTTCAAAAT | 286053 |
rs551528974 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182898 | TACCAGAAATAATAT[A/G]TCATTTCTGCACAGT | 286053 |
rs551529754 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344436 | TTCAATCTTTTTTCT[A/G]TATACCATTGTTTAA | 286053 |
rs551536887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122482 | CTATATACTCCAGTC[A/G]TGGAGCCTGGTTTAA | 286053 |
rs551547882 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256504 | ATGTCAGTGAGGCAG[C/T]TGGAAATACATGTCA | 286053 |
rs551548342 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284023 | GCTGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCTC | 286053 |
rs551557663 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301123 | TGAAATGAACAATCT[A/C/G]TGTGACCCATTTAGC | 286053 |
rs551557904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333765 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 286053 |
rs551561159 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159496 | GGAGTAATAGGCTTA[C/G/T]TATAGAGCCCAGGAG | 286053 |
rs551568738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326725 | CTTTGGGAGGCCGAG[A/G]CAGGTGGATCACCTG | 286053 |
rs551569138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095450 | AAAAAAGAAAAATTG[A/G]CCAAGTGGTGGCGCG | 286053 |
rs551597566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291091 | TAAAAAGATGTAATT[G/T]TGGTAAATATTAAGA | 286053 |
rs551623064 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140257 | GAAGATTTGTATTGG[G/T]AATATTGCAAAGTAC | 286053 |
rs551640819 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094651 | AGCTACCATAACAAA[A/G]TACCATAGACTGGGT | 286053 |
rs551643575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168121 | TCTATGAAAGATTTT[A/T]TTTTTTTTTGTGGAC | 286053 |
rs551650198 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145236 | AGTCCACAATGGTTT[A/G]GCATTGTGCTTGTGA | 286053 |
rs551650717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230968 | ACAATTTTTAGAGAC[C/T]CTGATAGAGGATTAA | 286053 |
rs551664179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202164 | TCCTCTGGCCCCTTG[C/T]GCTTCCTTCGTGAGG | 286053 |
rs551665334 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270554 | TTTAAATAGAAGCAA[A/G]TTATGATCAGCAGTG | 286053 |
rs551677541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292161 | GAAGAAGAGAGTATT[A/G]GTGACTGTTCTCAGT | 286053 |
rs551679192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327311 | ACCAAAATTGGGAAC[C/T]ATAATTGAAATATAA | 286053 |
rs551680391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152224 | CTTGTAAAATTTTGA[C/T]GTTTCTGGCTATTGT | 286053 |
rs551689082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260354 | ATCATCTGAATAGCA[G/T]TTCTCTACCAAGACA | 286053 |
rs551705566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194949 | ATTTATTCTTTAATT[C/T]ATTCCAGAAACACTA | 286053 |
rs551720970 | snp | A/T | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090229 | AATTTGGCTAGAGTA[A/T]TTGGTAAATAGCCCC | 286053 |
rs551737111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174718 | GGAAAGGTGTTTCCA[C/T]GTTTGGTTGGCTGCT | 286053 |
rs551761468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240886 | ACTGCATGGTATTCA[G/T]GCACCCCTGGTATCT | 286053 |
rs551802803 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105016 | GAAGAGAGTGAGACT[C/G]TGTCTCAAAAACTCC | 286053 |
rs551808765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210846 | ATGCCTCAGCCTCCC[C/T]AGTAGCTAGGACTAC | 286053 |
rs551818843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247758 | TTGTTTCACTAATGT[A/T]GCATTTGTTCATCAT | 286053 |
rs551821945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280801 | ACTAATGGAGGAAAT[A/T]TTTTTATCACATAAG | 286053 |
rs551823921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364813 | AATAAGGGTTCTCTC[A/C]CCATTTTAACTCAGA | 286053 |
rs551826195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160925 | TAATTGGGAGAGAAA[A/T]ATGTGTTGGATTTAT | 286053 |
rs551834320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253481 | GGTGGAGTTTTGTTT[C/T]TATGTTTGTTTGTTT | 286053 |
rs551838306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103536 | TCAAATTTGGAAAAA[A/T]TTCTGCTACTATTTC | 286053 |
rs551839765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249173 | AAGACTCTGTCTCAA[A/G]AAAAAAAAAAAATAG | 286053 |
rs551845923 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346473 | CTCCTTACCTTCTGA[C/T]CTTTGCTTTCTTCAG | 286053 |
rs551846695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104374 | CCTTTCTAGGCTTAT[C/T]GTTAAGCTTTGTTAG | 286053 |
rs551852131 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350161 | GAAGAGAACGAGGGA[A/G]GGGGAGTGGAGAAGA | 286053 |
rs551861989 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178729 | CAAAAAATTAGCCGG[C/G]CATGGTGACGGGCAC | 286053 |
rs551870109 | in-del | -/TAAT | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239716 | ACTTCCTTCAATAAA[-/TAAT]TAATTAGAGGCTGAA | 286053 |
rs551871189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211417 | ATATTTTGAATATTC[C/T]ATATCAGTACATATA | 286053 |
rs551876273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273055 | CCGCCTATCATAGAA[C/T]CTGACAGTTACTGCT | 286053 |
rs551885435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287316 | CAGCCTGGGTGACAG[A/G]GTGAAACTCTGTCTC | 286053 |
rs551903119 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241716 | AGTAGTGGTGATTTT[A/T]ACAAAAGTACTCATA | 286053 |
rs551934843 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246887 | ATAATTACCATTTTC[-/T]TTTTTTTTCTTTTTC | 286053 |
rs551978938 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337898 | TCAAAAAAAAAAAAA[A/G]AAAAAAAGAAAGAAA | 286053 |
rs551983648 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147927 | TTCTCATGACCTGTC[C/T]TTAAGATGCTCTTGT | 286053 |
rs551986464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322193 | GCAACATAGCAAGAC[C/T]GTGTCTCTACAAAGA | 286053 |
rs551988063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313620 | AGACTGAAGCAAAGG[A/G]AAAGTGTCCTCAAAA | 286053 |
rs551991817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202488 | GTAAGTTCAGATAGT[A/G]GCACAACCAAGTAAT | 286053 |
rs552001395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203451 | CCATAGGTCTTTGAG[A/T]TATATACAGCCCATG | 286053 |
rs552031477 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111065 | ATTGATTGAATGATA[G/T]TCTGTTCTTTCATAC | 286053 |
rs552034459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155293 | TTCAAGTCAAATGAG[C/T]CTCAACATGGGAAAT | 286053 |
rs552044932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335421 | ATTAGGTAACTTGCT[C/T]AAAAACACAGAGGGA | 286053 |
rs552051499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089933 | TATATATAAACTTTA[C/T]ATTAAATTTTTAATG | 286053 |
rs552058116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216056 | GACTATATCTGTCTC[C/T]TAAAACAAACAAACA | 286053 |
rs552063747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217512 | ACTACGGGCACCTAC[C/T]GCCACACATGGCTAA | 286053 |
rs552063906 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315107 | TTTTCTCATTGACTA[A/G]AATCTTTTTTTTTTC | 286053 |
rs552072862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365330 | CCATCGGCAAGTCCT[A/G]TAGGTTCTATGGTCA | 286053 |
rs552086858 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247202 | GCTGGGAGTAGTATC[G/T]TGTACCTGTAGTCCC | 286053 |
rs552094827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260849 | GGCTGATCTTTAACT[C/T]CTGACCTCAGGTGAT | 286053 |
rs552096997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343933 | ATGGCATGAACCTGG[G/T]AGGCAGAGCTTGCAG | 286053 |
rs552122174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225314 | GTGGGTCTCCTTTCA[G/T]CTTGTGGCTCTTTTA | 286053 |
rs552129570 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204279 | ACTACACTCTTAAGC[A/C]CAAAGTGTGGCTGCC | 286053 |
rs552137133 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367408 | TAATCCTAGCTACTC[A/G]GGAGGCTGAGGCAGG | 286053 |
rs552142582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132299 | TACAGACAGGGTCTC[A/G]CTATGTTGGCCAGGC | 286053 |
rs552157447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269863 | TGTAACAAAGTAAGC[C/T]AAACATAACTTGTTA | 286053 |
rs552175487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176240 | AGCCTTTGCGCATAT[A/G]TCTGCTCTTGCTAGA | 286053 |
rs552195769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307409 | TTGTCAGATCAGAAA[A/G]GGAATGTGATTCTTT | 286053 |
rs552198864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307981 | ATTTCTTTTTTTTAA[C/G]TGCCAAATCTGACAA | 286053 |
rs552204688 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134753 | TTTTTTAAGAGTCGG[G/T]GTCTTGCTCTGTTGC | 286053 |
rs552206098 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124909 | AAGCAATTATCCTGC[C/T]TCAGCCTCCTGAGTA | 286053 |
rs552233246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263727 | TGCACACCAGCCTCC[A/G]TGACAGAGCGAGACT | 286053 |
rs552248230 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293966 | TGTTAGCATTTACTT[C/T]CTATTTTCTCCCAAG | 286053 |
rs552260406 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295042 | CACCTGAAACTACTT[A/G]AAATAGGTTGGACTT | 286053 |
rs552263266 | in-del | -/AGAA | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125099531 | AGATGGAGAGGAAAC[-/AGAA]AGGAGAATGAGAACA | 286053 |
rs552275356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359931 | TGCAGAGATGGATTA[A/C]GGAGGCATGAGGCAA | 286053 |
rs552288566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170467 | CTGGAGTGCAAATGG[C/T]GCTGTCTCGGCTCAC | 286053 |
rs552295368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255858 | TGAAGCATGAAGACC[A/G]GTCAGATGGCCGTTG | 286053 |
rs552296003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276406 | TCCTTACTCCAGACT[A/G]ACTGGAGGACTGATT | 286053 |
rs552296179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270414 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC | 286053 |
rs552301540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176868 | CCTGGGACTTGTACC[A/G]TTACTTCACACAGTC | 286053 |
rs552332758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121017 | TTCATCACTATTTCA[C/T]TGTATTTCTTAAACT | 286053 |
rs552340764 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225316 | GGGTCTCCTTTCATC[C/T]TGTGGCTCTTTTAAG | 286053 |
rs552343382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134194 | ATGAATGTTTTCATA[C/T]TTAACAGAAAAACTG | 286053 |
rs552350296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163471 | TCCATGTTCTACCAG[A/G]CTGTGACCTTGGACA | 286053 |
rs552352450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323373 | AAAAAAGGACAAAGT[C/T]AGAGAACTTATTCTA | 286053 |
rs552376129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242758 | CATAGGTACTAGAGA[A/G]CAGAGTCCCCCACTC | 286053 |
rs552401537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358695 | GTGACTAGTTCTCAA[C/T]TGACTTCTGATAACA | 286053 |
rs552407293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273838 | ACCTGTGAGTTTGGG[A/G]TGCTGTATAAATGTT | 286053 |
rs552437890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184091 | GTATTTTATTTGACT[A/C]TTTGGAGCCAGTACT | 286053 |
rs552465084 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242085 | TCTAATGGAAGTGTA[C/T]CTCTATGTAAACAAT | 286053 |
rs552467902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098797 | GGAGTAGGTTTGGGG[A/G]AGGGGTAGGGTGGGA | 286053 |
rs552469688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268645 | TATCCAAATTTAATG[C/T]TAATGTTTCAGCAGA | 286053 |
rs552478802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141053 | ATAGCCTGAGTTTCC[A/G]TAGTGTTTTTGATGG | 286053 |
rs552492556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281671 | TCTCGAACTCCTGGC[C/G]TCAAGCAATCTTACC | 286053 |
rs552507640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316822 | CTTGCTCTGTTGCCA[C/G]GCTGGAGTTGAAGTA | 286053 |
rs552518553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133254 | AATAGATGTGAGTAA[A/C]TGACTAGGATATTTA | 286053 |
rs552548839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268168 | GAGCCTGGGAGGTCG[A/G]GGCTGCGGTGAACCA | 286053 |
rs552573501 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172049 | TTAATTCATTTAATA[C/G]TCAAAGGTTAAGTAG | 286053 |
rs552582930 | snp | A/C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308124 | TTTGTTTCCTAGTCT[A/C/T]GGAGGCATGGGAGTT | 286053 |
rs552598532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354089 | GGCGCCCACCACCAC[A/G]CCCAGCTAATTTTTG | 286053 |
rs552601046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198997 | TTTATAGTATTCTCT[G/T]ATGGTAGTTTGTATT | 286053 |
rs552628255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178585 | TTAAAGAAGTCATTA[G/T]GTTGGCTGGGCGTGG | 286053 |
rs552634266 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141257 | CAATTTATTTAAGTC[A/C]ATCAGTCTCTCTTTC | 286053 |
rs552635967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324879 | GCGCCCGGCCCATTT[G/T]GATAAAATTCTTTAT | 286053 |
rs552641047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310121 | GGAAACTAATCGTTT[C/G]TGTAACTGGCAGGAT | 286053 |
rs552644949 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304796 | TTCTCATCAAGCGAT[C/G]AGAATCGCTTGAACC | 286053 |
rs552646185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112993 | AACAAAATGTATACC[A/G]TAAATATATTTAATT | 286053 |
rs552648821 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333775 | GCCTCGGCCTCCCAA[A/G]GTGCTGGGATTACAG | 286053 |
rs552656752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127129 | CATGAAAAATATGGA[C/T]ATTATCTCCTTTTCA | 286053 |
rs552657682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228680 | AATGTCCCAGAGAGT[A/C]TGGTGTGTTACATGC | 286053 |
rs552677137 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251155 | AGTTTAATAAGGGAA[C/T]AATATAGTCAGCTAT | 286053 |
rs552687313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360431 | TCGCCTGTGATCTCC[A/G]CAAGGCCAGAGCCCG | 286053 |
rs552688496 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360249 | CGTGGAAGTGTCCAG[C/G]AAGTGCAGCAAGTGT | 286053 |
rs552692474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276620 | CATAGAGTGTCTGAC[C/T]TATGGTAGAACCTCC | 286053 |
rs552705827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331617 | CAAAATAACCAGATT[A/C]TTTTTATACACTTTT | 286053 |
rs552711082 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325594 | TCAAGCAATCTGCCC[A/G]CCTCAGACTACCAAA | 286053 |
rs552711883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091232 | CCAAACTCACAGCCC[A/G]TGGCATAACTAGAAT | 286053 |
rs552715090 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111508 | ACCTTTCATGTTCAA[A/G]ATGTTTTGAGGCTGG | 286053 |
rs552726747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193239 | AAATTAAAACCTCCA[A/G]CTTATCACGACAGAC | 286053 |
rs552734837 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288865 | AGTGGCTCGATCTTG[G/T]CTCACTGCAGCCTCA | 286053 |
rs552789783 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186029 | CTAGGCCTGGGGTCA[G/T]TAAACTCTGGGCCAT | 286053 |
rs552795742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288471 | CTCTGAGCTATTTCT[G/T]TTGATTGATTGATTG | 286053 |
rs552797548 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295500 | GAGTGATCATCCTTT[C/G]TGACCCCCTGAGAGA | 286053 |
rs552820742 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098087 | AATTCTTGGATCAGC[A/C]AAATCTACATTACCT | 286053 |
rs552830142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185586 | GTTGGGATTACAGGC[A/G]TGAGCCACTGCACCT | 286053 |
rs552834358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157061 | ACCTATTATATATGA[A/C]CACTTACTGACTGAA | 286053 |
rs552843531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235194 | TGCAGTGAGCCAAGG[C/T]CGTGCCACTGCACTC | 286053 |
rs552848147 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200362 | GAGCTCTTGTAAGGC[A/C]GGCCTAGTGGTGACA | 286053 |
rs552849754 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106328 | TCAGAAAAGTCATAC[A/G]CTCTCAAATTTATAA | 286053 |
rs552849812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099020 | GGAGATACATAGTAT[C/T]ACATTCATTCCTTCT | 286053 |
rs552867248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282043 | GCTAGAGAGCAAATA[C/T]CCTGTGTAGTGTTGC | 286053 |
rs552878619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281907 | AAGAATCTTAGAAGG[C/T]TCCAATATACTTCCT | 286053 |
rs552900439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237721 | TGCATTCCTGAGTCC[A/G]GTCAGTGAGACCGGG | 286053 |
rs552909138 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250383 | TCTAGCCCTCTTACT[G/T]TAATTAATCCAAAAA | 286053 |
rs552909846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192126 | TGCCATCCACACTCA[C/G]AAAGTAGCCTGAATC | 286053 |
rs552911640 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202590 | TAACTAGCCCACAGA[A/G]TTGTTTATGGGTTAA | 286053 |
rs552929282 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218599 | GTATTTTTAGTAGAC[A/G]TGGGGTTTCGCCATG | 286053 |
rs552930995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189679 | AAGGAAGAGAAAAAT[A/G]GAGGACAAAAATTAG | 286053 |
rs552935774 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091924 | AGGCAGGGGAAATTG[A/G]GGTGCCACCAGACGG | 286053 |
rs552952127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283029 | TGTGCTTCTTGACAG[C/T]TGTGTGACCTTGGGT | 286053 |
rs552961178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227804 | CACATAATAACATTT[C/T]GTGGTTTCTTTTAGT | 286053 |
rs552967900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245022 | GCTCTGTGGCTCACA[C/T]CTGTAATCCCAACAC | 286053 |
rs552969749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341558 | TGTGGTTTTTGTTAC[C/T]GCGTTGATTCATCTG | 286053 |
rs552986940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332509 | CTATAAAATAGTTAG[C/T]GTAGAAGCTGGTGCA | 286053 |
rs552993533 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270177 | TGACTTACTAAAGAA[A/T]CTGAAAGGTCCAGGT | 286053 |
rs552999638 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125127977 | GTGGTGTCATGTCAG[C/T]GCTCAAAAAAGCTTT | 286053 |
rs553006397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354389 | GAAATAAATCCAGCC[C/T]TACATATTACTTCCA | 286053 |
rs553007253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199372 | CCCAGAGATTCTGGT[A/C]CGTTGTATCTTTGTT | 286053 |
rs553027460 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306909 | CTTAGCATTATGTGA[A/G]GAATAATAAGTTAAT | 286053 |
rs553032262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236738 | AAAGATTTGACTAAC[A/T]TCTCTGCCCACTGAT | 286053 |
rs553039312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238259 | AGGTTATAGAAACTT[C/T]TTATTCCATTTCCAT | 286053 |
rs553040783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360793 | TGTTTAGAAATGTCC[A/G]TGACACATTGTCTCA | 286053 |
rs553069205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263907 | TGCCTAGAACAATTC[C/G]TAACACCTGGTACTC | 286053 |
rs553075070 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241802 | ATTTAGTAATTGAAT[G/T]TATTCCTTCCACAAA | 286053 |
rs553091810 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091465 | AGCTGGATTACAGCC[C/T]CCGCCCCAGAAAGCC | 286053 |
rs553108814 | snp | A/G | | | missense | NSMCE2 | GRCh38.p7 | 8:125357248 | GACAGAGAAGCTGAC[A/G]GAACAGAAGGAGTGG | 286053 |
rs553130535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270649 | CAGCAACTCAGTAGG[C/T]TGAGATGGGAGGATC | 286053 |
rs553132210 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263581 | ATGGTGAAACCCTGT[C/G]TCTACTAAAATACAA | 286053 |
rs553135844 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247598 | GGTATGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 286053 |
rs553137488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347744 | TTCAATGAAAGGAGA[C/T]TGGCTATGGAGATTG | 286053 |
rs553137579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206598 | ACTTAGGAGAACAAG[C/G]AGTTGAAGTTGGCCA | 286053 |
rs553138782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135713 | TTTGTCTGTTTAGTT[G/T]TCCATGTAGGTATAT | 286053 |
rs553187277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326824 | AGCCGGTCGTGGTGG[C/T]GGGCACTTGTAATCC | 286053 |
rs553194186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276035 | AGAGGTCTGCCCCCC[A/G]CACTGGGTCTTCTGT | 286053 |
rs553194774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107273 | CTCACTGCAACCTCC[A/G]CCTCTTGGGTTCAAG | 286053 |
rs553199128 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157886 | AATCAGGATGTGAAT[A/G]AGTATAATAGGAAAA | 286053 |
rs553201438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194405 | TTTGACATTCATTAA[C/T]AGTATTGCTAGTTAT | 286053 |
rs553212468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324408 | CTGGAAACAAGCCCA[A/G]TATCCCGTAACTGAT | 286053 |
rs553213015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213127 | ATTTGGCTTTGAAAG[A/G]GTCGACCTGTATGAA | 286053 |
rs553223970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333803 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCTTCCTG | 286053 |
rs553226370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338887 | CATCTTAGCATCTCA[A/G]TTTAGGCCAAAGATT | 286053 |
rs553230984 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296375 | TTGGCTGTAGTCAAA[C/T]TGTTGTTGCCATGGT | 286053 |
rs553249032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225771 | GCTATCTGCAAGGAC[A/G]TTTTAGTTTTCACTT | 286053 |
rs553257476 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282453 | GCTATTGATTGAAAT[G/T]TGAAATGCAACGTTT | 286053 |
rs553265865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331796 | GTTTCAGCGTATAGC[A/G]TGGTCCACTTCTTGC | 286053 |
rs553265872 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101739 | TTATAGTGGATGTGC[A/T]GCCAGAAGACAAGTT | 286053 |
rs553270196 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221416 | GCCTGGCTAAGTTTT[G/T]TATTTTTTGTAGACA | 286053 |
rs553291880 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235981 | CACAGATTTCTATTC[A/C]TGGAAATATGGCAGT | 286053 |
rs553301111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348370 | TTTGCCATCCTGTGA[A/G]GTTGTAACATCTAGG | 286053 |
rs553305747 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272777 | TATATACACACACAC[A/G]TATATATATACACAT | 286053 |
rs553308939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195179 | GAGGTGCTCACCCAT[C/T]CCTAGGCGTCAATAT | 286053 |
rs553309341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160450 | AGGGCCTCTTTCCTC[A/G]GAAGGGGTTGGGGGT | 286053 |
rs553321345 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114963 | GTTGATAGCATTCCT[C/T]GTGTTTCCCTTATAT | 286053 |
rs553332459 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281090 | GTGACAGTTATAAGC[C/T]GATTAAGATAGCTTT | 286053 |
rs553335935 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342839 | ACCACTTTGTCAGGC[C/T]GTGGAGCTGAGCTAC | 286053 |
rs553343420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144367 | GTTAGCCATGCCCAC[C/T]TGGATTTGGGAAAGC | 286053 |
rs553348757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121216 | TAGATGAAGAAGGGA[A/C]AGAGAATATTTATAA | 286053 |
rs553354446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259753 | TTTATGTTTATTAAA[C/T]GTTGGTTTCAACAAC | 286053 |
rs553372716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152911 | AAAATACAAAAATTA[G/T]CCAGGTGTAGTGGCA | 286053 |
rs553376277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153674 | CCTGGTCAAGAAACC[A/T]AACCTCTTGAAAACT | 286053 |
rs553384645 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117002 | AAACAGTTTTCCTGC[C/G]TTAGCCTCCCAAGTA | 286053 |
rs553408611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114127 | TGAAATTTAGAATTG[C/T]AGCATGTCCTTCATC | 286053 |
rs553408760 | in-del | -/ACATGGTGAAATCCCATCTGTACAAAAAATACAAAAAAATTAGCCAG | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223170 | AGACCAACCTGAGCA[lengthTooLong]ACATGGTGGTACACA | 286053 |
rs553421208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229795 | GTTTTATTATTTGAT[A/G]GATGATAAATGATGA | 286053 |
rs553439569 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246026 | AAGACTCCATCTCAA[A/G]GAAAATATGAAATTA | 286053 |
rs553446063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159720 | TGCTTATTAGTCTCA[A/G]ATTGCTCAGTTGGTG | 286053 |
rs553451082 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351160 | AGAACCAAAGGCAGA[A/G]CTGCTTGGCTCTTCC | 286053 |
rs553456059 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277567 | GCTGGAGTGCAGTGG[C/T]GCGATCTCAGCTCAC | 286053 |
rs553457233 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298706 | TTTTTTGTTTTTTTT[G/T]TTTTTTCCCCAGTTT | 286053 |
rs553473681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201929 | GTCCCCCACCCCATT[C/T]CCCCGCCTTCCTGCG | 286053 |
rs553511075 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285293 | GTCACATCGACACAA[G/T]AAAGTGACTTTTTAC | 286053 |
rs553513338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114767 | CACACTAATGTATGC[A/G]TACATACATACATAT | 286053 |
rs553517317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200128 | TTGACTCTTTATCCA[A/G]TTTGCCAGTCTGTGT | 286053 |
rs553518616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305123 | TTCCAGCTTCAGAGG[C/T]TGGATAAATGGAGAT | 286053 |
rs553533308 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257726 | TTTTTAGTAGAAACG[A/G]GGTTTCATTGTGTTA | 286053 |
rs553535133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195860 | TTATGTTAGTCATTA[C/T]ATTCTTTTTCCTGAA | 286053 |
rs553548198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362612 | CCTTCATGTTCTTAA[A/G]GGGAAAAACTGAGGC | 286053 |
rs553551947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150633 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTAC | 286053 |
rs553557210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166083 | GGATTGCCCTCATTC[C/T]GGGCTGTGGACATGT | 286053 |
rs553563315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158128 | ACCCCCTAATTTTAC[A/G]AAGGAGGCTGTGAGA | 286053 |
rs553606231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264467 | GCTGGAATGCAATGG[C/T]GCGAGCTCGGCTTAC | 286053 |
rs553619772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129723 | TCATGTAAACTTTTT[A/T]AAATGCAACTTCATC | 286053 |
rs553624140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137583 | TCCTGCTCCTTTTTT[C/T]ACTGGTGTGGTTTCT | 286053 |
rs553634953 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107319 | GCCTCCTGAGTCCTG[-/A]AGTAGCTCGGATTAC | 286053 |
rs553650484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222284 | ATTTATGGAATACAG[C/T]GTGTTTTGATATATG | 286053 |
rs553654567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173604 | TCTTGAGTGAGATAC[C/T]ATGGTGATGAATGAG | 286053 |
rs553675569 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265377 | CAGGCATGCACCACT[A/G]TGCCCGGCTGATTTT | 286053 |
rs553679249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122953 | AACAAATGGATGTGA[C/T]TTGAATAGTAGTGGG | 286053 |
rs553679279 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266168 | GCGATCTCCGCTCAC[C/T]GCAACCTCCGCCTCC | 286053 |
rs553690446 | in-del | -/AAATC | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262107 | TCTCAAAATAAAATA[-/AAATC]AAATAAAATAAAATA | 286053 |
rs553694921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165524 | CTGGAAACAGTGGTT[G/T]AATGATATTATCTTA | 286053 |
rs553704381 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313710 | CTTAGAGTTTCCTTG[C/T]TCCCCATACTCTTCC | 286053 |
rs553705114 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289653 | TTAAATGTTTGATGA[A/G]TAATGAAGGAATATA | 286053 |
rs553711804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231160 | TTACAGTCCTAGAAA[A/G]AAGCATTAATTATAT | 286053 |
rs553714004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167111 | AAGGCAGACTTCTTT[C/G]ACTTTCACTGTGCCT | 286053 |
rs553753020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356258 | GGTGTTCTGGAAATA[C/T]AATTTTAACTTTTAA | 286053 |
rs553765297 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313115 | TGGAAAAAAAAAAAA[A/G]GGAAAGAAGGAAGGA | 286053 |
rs553785031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109249 | CTCCAATTTGCCTCA[A/G]GTTTCCTATTTATAA | 286053 |
rs553786693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123638 | TGTGCATCTTGTGTA[A/G]ATCAACATGTCCCAT | 286053 |
rs553791573 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184453 | TTATGTATATTTATA[C/T]TGAAAGAAATACTTC | 286053 |
rs553797472 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245339 | CACATTCTCTCACCA[-/T]TAATGCTGACAAATA | 286053 |
rs553833892 | snp | C/G | 3.3117e-05 | 0.00406908 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102307 | TGTTTCATTGTGTTT[C/G]AAAACTTAGGTACTA | 286053 |
rs553835508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299305 | AAGGAGCACTCTATT[C/T]GTTTCTTTTCACACT | 286053 |
rs553839337 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345910 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG | 286053 |
rs553845253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183292 | GCCTCACTTTTGTCT[A/G]TTTTACAAATAACTT | 286053 |
rs553862649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207703 | TTGGATGGGGTTTAG[C/T]TGGGTGAGTCTTCTG | 286053 |
rs553864450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215666 | GGTTTTTATGGTTTT[A/G]GGTCTAACGTTTAAG | 286053 |
rs553877525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117256 | AGACAGAGTCTTGCT[C/T]TGTCACCCAGGCTGG | 286053 |
rs553907288 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289283 | AAGTATCACTCATGC[A/G]GCTGTTGCAGGACAA | 286053 |
rs553913409 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280368 | GTGTTTCTAAACTAA[-/T]GAAATGTCCTTTCTA | 286053 |
rs553925923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108427 | TGATACTAAGGCAGC[A/C]AGTATCAGCACTTAA | 286053 |
rs553931993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208389 | TGTATAGGAATAGAG[A/G]AAAAGAAACATGGGA | 286053 |
rs553942139 | in-del | -/T | 0.000272524 | 0.0116699 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151154 | AAATAATAATTGCAA[-/T]TTTTTTTTTCTTTCA | 286053 |
rs553953096 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179536 | ATAATGAGTTGAATG[A/T]TTTTAAATTTCATTT | 286053 |
rs553962938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311547 | TGCTTTATTCGTGGT[A/G]TGTTGTGCAATATGT | 286053 |
rs553962975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319022 | GCCAGGGAAAGAGCT[A/G]TCTAATGGATTAGAG | 286053 |
rs553968667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175300 | TATTTGTTGAATGAA[C/T]GTTCTAGGATCAGTT | 286053 |
rs553975164 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300171 | AAGGGCTGTGCCTCT[G/T]TTTTTTTTTTTATTT | 286053 |
rs553986168 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285864 | AGATGAGGTAACTGA[A/T]GCTTGGTGAGGTTGA | 286053 |
rs553995924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280301 | AAACAGACCCAAATA[A/C]ATCCTCAGAGAGAGA | 286053 |
rs554007068 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156385 | CTTCACTTTCCTCTA[A/G]TACCCTCTTTTATGC | 286053 |
rs554028561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153668 | ATGATCCCTGGTCAA[A/G]AAACCTAACCTCTTG | 286053 |
rs554028978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304610 | ACCTGTAATCCTAGC[A/G]CTTTGGGAGGCTGAG | 286053 |
rs554037312 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223033 | TGCCAGTGCACTCCA[C/G]CCTGGGCAACAGAGT | 286053 |
rs554043496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355737 | AGCTATTGATCTTTA[A/G]CTTCTGTGCAAAATT | 286053 |
rs554043590 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146466 | GTTTATTGCGGCACT[A/G]TTCACAGTAGCAAAG | 286053 |
rs554044342 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297833 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAATTATT | 286053 |
rs554051421 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189112 | ATAAGGTATAACTGT[G/T]GTTAGAAATAGATAA | 286053 |
rs554065674 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287431 | CCTGCTGCTACTGTT[-/C]CTTTCCACAGATGCC | 286053 |
rs554071993 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272236 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 286053 |
rs554102831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225360 | TCTTTCTGTCCTTTC[A/G]ACTCCATTCACCTCA | 286053 |
rs554107882 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142123 | GACTAATTACACTTG[C/T]AGAATAGTTATCTAT | 286053 |
rs554113343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180912 | GGCACTGGTAATACC[A/G]TGATAAATCAGACAT | 286053 |
rs554122698 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232603 | AGAAGGAAATTATGA[G/T]GGAAAATTTCAAACA | 286053 |
rs554148594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320299 | GGAAGGAAGGAAGGA[A/T]GGAAGGAAGGGAAGG | 286053 |
rs554149714 | snp | A/G | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362181 | TGCCACACTGAACTC[A/G]CTCACCAAGATGTCG | 286053 |
rs554151414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254627 | TTTTTTAATAAAGGA[C/G]TATAATTTGATTGGC | 286053 |
rs554161321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242112 | CAATAACTGGGGGGG[A/G]AGTTTGAGAACCACT | 286053 |
rs554167604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330321 | GCTGGAATTACAAGC[A/G]TGTGCCACCACACCC | 286053 |
rs554185930 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261205 | ACTTATTGACAATCA[C/G]TATTATGCTGGATAC | 286053 |
rs554190394 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203743 | CTAGTCTCTTGAGAT[A/T]ACAAGGTCCTAGAAA | 286053 |
rs554203688 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364969 | AATTTGGTTCACTTT[A/G]AGAACCAGATTCTTT | 286053 |
rs554207741 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267002 | CTTTTCTTTTTTCTT[G/T]CTTTTTTTTTTTTTT | 286053 |
rs554210471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366337 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 286053 |
rs554239084 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272945 | TTGGGAGCTAGGCCA[C/G]GGTTGAAACCCCTCC | 286053 |
rs554243666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217045 | CAAAGATTTATTAAG[C/T]ACCTATACTATATGC | 286053 |
rs554251139 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201011 | TGTGCCTTGGTTTTC[A/G]GCTCTATCAATTCAT | 286053 |
rs554259739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097520 | GAACAGCTCTCCCTG[A/G]TAATTTAGACCTTTC | 286053 |
rs554272786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261212 | GACAATCACTATTAT[A/G]CTGGATACTATGGGA | 286053 |
rs554277391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141129 | ACTTTATTTCAAACA[A/G]TATTTTGAATTATAC | 286053 |
rs554280044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331050 | CTCACACCTGTAATC[C/T]CAGCACTTTGGGAGG | 286053 |
rs554283137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131823 | AAGTTTGAGAGCCCT[A/G]TCCCCTCACTTTGAA | 286053 |
rs554296501 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343219 | CATTACAATCTGAGG[A/G]CAGCGCTGAGCACTA | 286053 |
rs554298820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095466 | CCAAGTGGTGGCGCG[C/T]GCCTGTGGTCCCAGC | 286053 |
rs554314276 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170161 | CTTCTCTTCATTTTC[A/T]CTTTATTTCATTCTC | 286053 |
rs554328946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203555 | TAAGAACAGTTTTAA[C/G]TTCATAGCAAAATTG | 286053 |
rs554332460 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267369 | TGAGACAAATATGTG[C/T]AAAGGCTTTCGTTTG | 286053 |
rs554344287 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124626 | CTGGGACTATAGGCT[G/T]GCACCACCACACCTG | 286053 |
rs554344566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132499 | TAAAAAAAAATTTTG[G/T]TTTTTTTTTTTGAGA | 286053 |
rs554350247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138940 | CCTCAATTTCCTCAA[C/T]CATATGAAGCAGAAA | 286053 |
rs554358190 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247282 | AGGCTGCAGTGAGCC[A/G]TGTTCATGCCACTGC | 286053 |
rs554373923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307590 | CACTGAGCACTTCCC[C/G]TAGCTTGCCCTAGAG | 286053 |
rs554381957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274703 | GGGAGGCCAAGGCAG[A/G]CAGATGACCTGAGGT | 286053 |
rs554385512 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242548 | AAACTTGGTTCCAGC[A/G]AGAACTGTTAGCTTA | 286053 |
rs554444205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329599 | ACACCTGTCTAGCTT[A/G]TTCCGATATACTGGG | 286053 |
rs554451481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111669 | GCTGGGTGTGGTGGT[A/G]TGTGCCTATAATCCC | 286053 |
rs554453556 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197573 | TATCTGTTTTGGTAC[C/G]AGTATCATGCTGTTT | 286053 |
rs554455065 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133102 | CTCTATGAAATGATT[-/A]AAAAATTTATTAATT | 286053 |
rs554458567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196628 | TGGGTTGGTTCCAAG[C/T]CTTTGCTATTGTGAA | 286053 |
rs554465921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210870 | GGACTACAGGTATGT[A/G]CCAATATGCCACTAT | 286053 |
rs554472202 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186025 | AGATCTAGGCCTGGG[C/G]TCAGTAAACTCTGGG | 286053 |
rs554488123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147031 | ACATATATAATCATT[A/G]TCATTACTTTCCATG | 286053 |
rs554493345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146149 | TAACAGATTGCCAAC[A/G]GAGCTGAGCTGAGGC | 286053 |
rs554498017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232873 | TGAGACTAAAGGACT[A/G]TTATGTGAATGAGTT | 286053 |
rs554504033 | snp | A/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110701 | TATTGTGCCAGCGTC[A/G/T]TGGCCTGTGCAGTCA | 286053 |
rs554522525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103050 | AGGCCGGCAGATCAC[A/G]AGGTCAGGAGTTTGA | 286053 |
rs554575458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184677 | AGTGCAGTATTATTA[A/C]TATAATACTTGTATT | 286053 |
rs554581375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288176 | CTTTCTACTGACTTT[C/T]CTTTTGTCATTTCAT | 286053 |
rs554612108 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320125 | AGGTTTCAATGAGCC[A/G]AGATCACACCACCAC | 286053 |
rs554623584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156508 | TCCTACTAGAAGCCT[G/T]GTGAGGGAGAATATT | 286053 |
rs554632368 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147864 | ACAAAAAAGAATTAC[G/T]AAAATCCTCTTAAAA | 286053 |
rs554637295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177233 | GTCTTCACAGCACTG[A/C]AGTGGGTGTTCCTGA | 286053 |
rs554654547 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285514 | ATAAGAATAGGGTAG[C/G]CATAGTTTCTGCTCT | 286053 |
rs554660599 | snp | A/C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172971 | TTGGTGGTCCTGCCT[A/C/G]TATGGAGTTATTTCT | 286053 |
rs554660905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191569 | TGCATTTAGAGATTA[A/G]GGAGTAGTAATGATA | 286053 |
rs554686955 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157303 | AGACTCACCTCTTCT[C/G]TACTCGCTGCATATG | 286053 |
rs554695400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140519 | AATACAAAAATTAGC[A/T]GGGCGTGGTAGTGGG | 286053 |
rs554717992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301090 | CAAAAAAAACTTTGA[A/G]CCATGCCTTTTTGTC | 286053 |
rs554743225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251031 | CAGAAAAATTATATA[A/G]CAGCTGTTAAAAGTA | 286053 |
rs554747366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164565 | TGGCGTGTGTTAGAG[A/G]GGGATTCTATTAGAA | 286053 |
rs554762016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162898 | AGTCATCTTTTTCAT[A/G]AAGGTTTATTCCTGT | 286053 |
rs554765704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296211 | AGGTAAATTTAGTGT[G/T]GTCATGTGCAGTTTG | 286053 |
rs554770773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227098 | TTAGAATTAACCTTT[A/G]CTAACAGGTTTAACC | 286053 |
rs554789849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113101 | AATATGAAAAATCCA[A/G]CTTTGAAAAACTCAG | 286053 |
rs554792329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347579 | ATAAATGCAAGTCTA[A/G]TTGAGTTAGCTTCAC | 286053 |
rs554799575 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198207 | CTGATTGCCCTGGCC[A/G]GAACTTCCAACACTA | 286053 |
rs554805051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262056 | GAATTGAGATTGCAC[C/T]GCTGCACTCCAGCCT | 286053 |
rs554811810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134259 | TTCTGAGTCATTATG[A/G]TGAGATTTCATTATA | 286053 |
rs554813827 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126180 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCTTGGCC | 286053 |
rs554818088 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140937 | ACAAGAAAGATGTGG[-/A]AAAAAAGATAAGTCA | 286053 |
rs554818528 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316214 | TAATTTGAGGTAGTT[C/T]CTACACAGTTTTCTT | 286053 |
rs554832954 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283220 | GCCACTTCTGCTGCT[A/G]TTGTTTTTAATTAAG | 286053 |
rs554849081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293999 | CCCCAGCTCTAGGCA[A/G]CCACTAAATCTACTT | 286053 |
rs554879111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126793 | AAAATAGCAGTTAAC[A/G]TCTAATAAGTATTTA | 286053 |
rs554883293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360081 | GAAAGGAAGAAGCAG[C/T]GAGGGGTGGCTGACA | 286053 |
rs554894329 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311563 | TGTTGTGCAATATGT[C/G]AGCATTTCCCCTTTC | 286053 |
rs554895441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310815 | AATGTTTGCATCATA[C/T]CTGCTGTTGAATTAC | 286053 |
rs554901693 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172917 | CTGACAACACTTTAG[A/G]CTGTCATTCACAGGG | 286053 |
rs554923598 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165266 | AAAGATGAGGCCTCA[C/T]GTAGCAGGCATTCAG | 286053 |
rs554942765 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255394 | CAGTGATATTTACTA[C/T]GTATCACAGGAACAC | 286053 |
rs554957877 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213158 | AAAGAAATGTTGAAC[A/G]TTTGTACCCTTTTTT | 286053 |
rs554962465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346923 | TGATAACATGAAAGG[G/T]TATATCTTACTAAAA | 286053 |
rs554968862 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331216 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 286053 |
rs554992927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193373 | TAATAATAAGAGACA[A/G]CACACTTCTGTTTAA | 286053 |
rs555000056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270010 | ACTAGTCTCTTTACA[A/G]ATAATGAGAATTTCA | 286053 |
rs555008601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112318 | TAAATCAGTACAGTC[A/G]TTATGGAAAACAGTA | 286053 |
rs555018027 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360506 | CCTCAAAAAACACTT[C/T]GTTGACCAATGAGAG | 286053 |
rs555026598 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303708 | AATGGAGAGTAAAAC[-/A]GAGAGGAAATTTAAA | 286053 |
rs555028249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302518 | TGGCTTTTACTTAGA[A/G]GTTAATATGGGGTGA | 286053 |
rs555028742 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091254 | AACTAGAATGCAAAT[C/T]CACGTCTGTCAGCCT | 286053 |
rs555030400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099064 | TGTTGAATGGCCACT[A/C]ATGTGCCATGCGTTG | 286053 |
rs555038154 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180007 | TAACATCTTAGGTGG[A/C]TGTGAGTCCATTTTA | 286053 |
rs555040150 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172419 | AACCTCTGTGTACAC[C/T]TTTTTCCAAGACTTA | 286053 |
rs555049392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199959 | CTCTTGATCTTTGTT[C/G]GTTTAAAGTCTGTTT | 286053 |
rs555050228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288987 | ACTTTTTATAGAGAT[A/G]GTCAGTGTTGACCAG | 286053 |
rs555060691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204621 | GTAGCTTGTTTATGT[A/G]CATTTTCCTCCTGCT | 286053 |
rs555061155 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340019 | TTTTTTTTGTTTTTT[G/T]TTTTTTTTTTTTTGA | 286053 |
rs555062179 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213874 | TGTGCCTTTCTATTA[C/G]TCACTATTCTGACCA | 286053 |
rs555066036 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271390 | AAATTTGAAAGATAT[G/T]TGGAATGTTGTGGTA | 286053 |
rs555090389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166147 | ACTTACTATTTATTA[A/G]AAAAGTCATGGCACT | 286053 |
rs555102061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105257 | TAATCTTTTTAGTGG[G/T]TGGCCTCCAAATGTT | 286053 |
rs555111641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218474 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 286053 |
rs555126497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338947 | CGCTCTGCCCTAGAT[A/T]TACAGTTGACATGAA | 286053 |
rs555142111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119591 | GCACTTTATTATATC[G/T]CTTTGATCATTGGAA | 286053 |
rs555150866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308735 | CCTTTTTCAAGCCAC[A/G]TGGCCAACCCACTCC | 286053 |
rs555166564 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135770 | TGTTGATCTCTTTTT[C/T]CATCTTCATGCCAAT | 286053 |
rs555175777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179486 | GAAACCATTAAAAAA[C/T]AGTTAGTGCCCATTT | 286053 |
rs555184119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282607 | AATTTTCAAACGGCT[A/G]TAACCTGGAGAAAGG | 286053 |
rs555240022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187082 | CTCTGCTAGCTCTAA[A/G]AGCTTTAGATTTAAG | 286053 |
rs555255407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186111 | GATTTTTATGTTTTT[A/T]AACTGTTGGAGAAAA | 286053 |
rs555281068 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226587 | TGATCCACTCGGATT[A/G]GTGTTGTCTGGGGTT | 286053 |
rs555298172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177934 | TTTGTGCTGCTTTCC[C/T]CAAGACAATAGCATT | 286053 |
rs555305269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327577 | ATCTACCATTTTGTA[A/G]TATGTGAGAGCTATA | 286053 |
rs555311012 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289420 | CTGCCCAAGTCCTGC[G/T]TATTCTCTTGGACTC | 286053 |
rs555340367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264079 | TGGCCCTCTGAATTT[G/T]CTCCAACGAACATAG | 286053 |
rs555351931 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112100 | AAAAATAACAATAAC[C/T]CTAAGAAGCCAATGT | 286053 |
rs555369700 | in-del | -/TTTC | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125129750 | CATCTCTTTTTGCAG[-/TTTC]TTTCACCTCATTTTG | 286053 |
rs555391793 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348439 | CCGTCTGAATTCTGC[A/G]AAATGTCTTCACATA | 286053 |
rs555400108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122018 | ATAAGTTCTTACCTA[C/T]GCATTATTGACCTAG | 286053 |
rs555436053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222518 | CTCCACATTTTCCCA[A/G]CCCCTTCCCCCTTCC | 286053 |
rs555466103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130417 | GTAGCTCGCTGTATC[C/T]ACACTCAAGGGGACA | 286053 |
rs555470656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213157 | AAAAGAAATGTTGAA[C/T]ATTTGTACCCTTTTT | 286053 |
rs555473979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128364 | GAAAGGTGGTAAGGG[A/G]TTGATGAGAAGTAGA | 286053 |
rs555481689 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147307 | CAATTTATATTTTAG[C/T]GAAAGTTTAATTTTC | 286053 |
rs555481941 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191409 | CCATTCATTTCTTGG[-/A]AAAAAAAAAATTGAC | 286053 |
rs555491791 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355001 | CTTCAGGCTATGTGT[A/G]TAAGCTTTATATGAA | 286053 |
rs555523149 | in-del | -/A | 0.174288 | 0.23826 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220643 | TTAACATCATTATTT[-/A]AAAAAAAAAAAAAGT | 286053 |
rs555529259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100933 | AAATTAGAATAACAA[A/G]ATAATTCTTTAAAAG | 286053 |
rs555536713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121310 | AAGATTTGCGCTTCC[A/T]CTTCTTTTGGGCAGG | 286053 |
rs555536718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129523 | TTCATTTTGAAGATA[A/G]TGTTAGGAAAAGATT | 286053 |
rs555543037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355129 | TGGTCCCAAGCATTT[C/T]GGATAAGGGATACTC | 286053 |
rs555555124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236877 | GAACAAGACCTGTCA[C/T]GTTTATTTTTCTTGT | 286053 |
rs555555198 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092871 | ATGCACTATTGACAT[A/T]TTAGGCCAGATAATT | 286053 |
rs555565883 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093594 | GGTGTGTCCTGGCAC[A/G]CACCTGTAATCCCAG | 286053 |
rs555566025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304468 | CCGGGGCAAGGAAAC[A/G]AGACAGCAAGTAGTT | 286053 |
rs555575159 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279428 | GACTTTTCTCACAAG[G/T]AAATGTATAATGGGG | 286053 |
rs555590873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188371 | ATTACCATAGCACAG[A/G]TCCTTGATGGTCACA | 286053 |
rs555596636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206727 | TTCATTAATGTCAAG[C/T]GTACTGAATTTAAGG | 286053 |
rs555609380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137649 | ATAAATCTTAAGAGC[A/G]AATTTGACAAAGTCT | 286053 |
rs555610143 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318416 | CTGACTCAAAAAGTA[A/T]AATAATGTTTACCTA | 286053 |
rs555611861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316916 | CCCGAGTAGCTGGCA[C/T]TATAGGCGTGTGCCA | 286053 |
rs555622325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236163 | TGAAACTTTTTGCGC[A/T]TAACGTAGAATTCAG | 286053 |
rs555629020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333998 | TTTTTTTCCACTACT[C/T]CTTCATGCTCCTGGG | 286053 |
rs555632353 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113361 | GGTGTGGTGGCATGC[A/G]CCTGTAGTCCTAGCT | 286053 |
rs555636743 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120059 | CAAATATGTCTAAAA[C/T]ATTTTAACATATAAT | 286053 |
rs555640757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252864 | GAGCGCAAGCTCCGG[A/G]AAGAGCCAAGGTTAT | 286053 |
rs555648659 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091983 | AAGCGGGGGACGGCA[A/G]TGGGGAGGGTGGCAG | 286053 |
rs555653635 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247201 | AGCTGGGAGTAGTAT[C/T]GTGTACCTGTAGTCC | 286053 |
rs555661855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207476 | GGTATTTTAAAATAA[A/G]TATTAAACATAAAAG | 286053 |
rs555662848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135207 | ACAGTTGTAACCTGC[C/T]GTGCCTGGCCTAAAA | 286053 |
rs555669352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361022 | ATATATCTGTTAACA[A/G]TAAGCCTATTTATTC | 286053 |
rs555692143 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210696 | ACCTAGCCATCTCTT[-/C]CCCAGGTTGATTTCT | 286053 |
rs555694987 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239302 | AACATCTTATGTTAC[-/A]AAAAAAATAGCATTT | 286053 |
rs555695564 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351774 | TCAGCACTTTGGGAG[A/G]CCAAGACAGGCAGAT | 286053 |
rs555697237 | in-del | -/AAAAAA | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367542 | AAAAAAAAAAAAAAA[-/AAAAAA]GAATGTCTTTCAAGT | 286053 |
rs555701767 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122896 | GTGTTGCACTACTCA[A/G]CTCTGCCATTTTCAC | 286053 |
rs555708121 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188911 | TAGAGAAGACTAGTG[A/T]TTGGAAAGGTATGTG | 286053 |
rs555715991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099766 | ATGGAAGGAGAGGAT[C/T]TGGAGACAAATGTAT | 286053 |
rs555717358 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142779 | CTGGCTAATTTTGTA[G/T]TTTTAGTAGAGACGG | 286053 |
rs555725840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306635 | TTTCCACTGACCATC[A/G]GAACAGAGAATTCCC | 286053 |
rs555734534 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126719 | CAAACACAGCTCTGG[A/C]AATTATTAGCATTGT | 286053 |
rs555735376 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218234 | CCAAAATACTAACCA[C/G]CATGTCTACTGTAGC | 286053 |
rs555744345 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146502 | GAACCAACCCAAATG[C/T]CCAACAATGATAGAC | 286053 |
rs555747469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114999 | GTTTCTTTATGTGTC[A/G]TATTTCCCTCACTGG | 286053 |
rs555778817 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146075 | AGCTTTCCAGAACCA[C/T]GTCTGATAGCCTCTG | 286053 |
rs555779274 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285547 | TAGGGTTTTGAAGAC[G/T]GACATAACAGATGTT | 286053 |
rs555780063 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185517 | TGCCATGTTGGCCAG[G/T]CCGGTCTTGAACTCC | 286053 |
rs555790786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290674 | TCCAGTGTGGTCCAG[A/G]CAACTGTGATCAAGG | 286053 |
rs555801376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116989 | ACCTCCTGGGTTCAA[A/G]CAGTTTTCCTGCCTT | 286053 |
rs555808758 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097173 | ATTTTTTCTTTTTTG[A/G]TGTGGAACTGTAAAG | 286053 |
rs555809276 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107381 | GTATCTTTAGTGGAG[A/G]CGGGGTTTCACCATG | 286053 |
rs555813266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341562 | GTTTTTGTTACTGCG[A/T]TGATTCATCTGTTAG | 286053 |
rs555832698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173769 | GTTTTCATAAAATTA[A/G]ATCTATTCTGTGTTG | 286053 |
rs555838702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284405 | CTAGCGGAGTCACAT[A/G]GGGGTTTGAGACTGA | 286053 |
rs555853263 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292337 | AGGTGGGTGGATCAC[C/T]TGAGGTCAGGAGTTC | 286053 |
rs555863254 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144409 | ATCTTCTGCTCTCCT[A/T]TCTGCTGTTGCTTTT | 286053 |
rs555894924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290158 | ATTTTTCATGACGTT[A/G]AAAAAAACTCCACTT | 286053 |
rs555911449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194513 | TTGAAGAACATCTCA[A/G]TTGTTTCCAGCTGGT | 286053 |
rs555914319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278742 | TTCATTCTGTAGTAT[A/G]AATTGCAGTCCCAGA | 286053 |
rs555915823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356351 | TTTTTTTTTTTTGAG[A/G]CAGAGTCTCGCTCTG | 286053 |
rs555915869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116380 | ATTTTTAAAAATGAG[A/G]TCAAAGATTTTCTTC | 286053 |
rs555993261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123071 | ATCAAAATATAAAGT[C/G]ATACCTGAAAAGGGA | 286053 |
rs556010740 | snp | C/T | 0.000576431 | 0.0169671 | synonymous-codon, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102399 | TGGTGTAGAGTCTGC[C/T]CTCTCCTCCTTGAAA | 286053 |
rs556012707 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323944 | AGTAAAAGATCTCTC[-/A]AAACTCAATAAGAAG | 286053 |
rs556045414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167687 | CTATGGAAGAAATTA[C/T]GCTAAAGGGATGGGA | 286053 |
rs556070939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245098 | ACCAGCCCGACCAAC[A/G]TGGTAAAACCCTATC | 286053 |
rs556082185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266210 | GATTCTCCTGCCTCG[A/G]CCTCCCGAGTAGTTG | 286053 |
rs556099110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169880 | TACACTAGCTCTTTG[A/G]ATGTTCTCTTGCCTC | 286053 |
rs556112038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103107 | CCCGTCTCTACTAAA[A/G]ATACAAAACCAACAT | 286053 |
rs556143245 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252355 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 286053 |
rs556151267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346607 | AGAAATAGAATGTGT[G/T]CATTAGATTTTCTGC | 286053 |
rs556175090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307035 | AAAACAGTGTGTTAA[A/G]ATGGGAGCCCAGCCC | 286053 |
rs556189577 | in-del | -/TTTCTCTTTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257517 | CTGGACAAAACCAAA[-/TTTCTCTTTT]TTTTTTTTTTTTTTT | 286053 |
rs556191373 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181958 | CTAGAACATGTCCCA[A/G]CCTCTCTGGTGCTTT | 286053 |
rs556202148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161201 | CTCACAGCATCAAGT[C/T]TCTGGTAATGGTGGC | 286053 |
rs556215286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215708 | TCTTGAATTGATTTT[C/T]GTATAAGGTGTAAGG | 286053 |
rs556230141 | snp | A/G | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367550 | AAAAAAAAAAAAAGA[A/G]TGTCTTTCAAGTGAT | 286053 |
rs556248725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301218 | CTGGTGGGAAAGGGG[C/G]CCTGAGGAAAATCAC | 286053 |
rs556249277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110719 | GCCTGTGCAGTCAAA[C/T]GACATTTAGCGACGT | 286053 |
rs556249561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344080 | GGATTGAAATGGTGT[C/T]ATAGCCCCATCTTAC | 286053 |
rs556273252 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209241 | TATTGATTGAAAAAA[A/G]ATAGAAACAAATAAT | 286053 |
rs556276849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261515 | AACTAAATTCTCTCA[C/T]TGGAGATTCAGCACA | 286053 |
rs556283785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328816 | CAGGGGAGTTATAAT[C/T]TTAAAATGTCACAGC | 286053 |
rs556293492 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172145 | CAAGGCAGAACTGGG[A/G]TTTAAAGGTTAAAGA | 286053 |
rs556309412 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314625 | CTCGATCACTCCCTG[A/G]AAACAACCAAGCCAG | 286053 |
rs556317167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216254 | ACCTTTTGGATATAA[C/T]GCTGCTGTGAGCATC | 286053 |
rs556320024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280409 | CTAAAATGTTCTATG[A/G]TTGCAACATCTGCTA | 286053 |
rs556327330 | in-del | -/TG | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101548 | CCATCCCTTTAAAAC[-/TG]TGAATTCTCCCCACT | 286053 |
rs556339725 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345235 | AATGTGACCTCCGTC[A/G]TCTTTCTTTTTGGTA | 286053 |
rs556345383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168254 | TGCTGAGATGTGCTT[A/C]AATAGATTCCATTGA | 286053 |
rs556353749 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323273 | TCAGAATCCCAGCAG[A/G]GGTTTTTTTGTAGAT | 286053 |
rs556394192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274251 | AATACAGAAAATGAA[A/C]CAAAAAAAAACTTTT | 286053 |
rs556456605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273223 | GAGACATTTTGGTAT[C/T]GAGTCAACCAGATAC | 286053 |
rs556464257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350421 | CTTGGCATGTTCCAG[A/C]AACAGAAAAGGCCAG | 286053 |
rs556489745 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349223 | GGCACAGATACATAC[C/T]CACATGCTATAACTA | 286053 |
rs556490893 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217646 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 286053 |
rs556494560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307713 | CCTCTAAAACCCCAC[A/G]AAGTAGAGGTATAAA | 286053 |
rs556495671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174303 | CCACATGTGGTAGAT[A/G]TTCAGTAAATATTTA | 286053 |
rs556499179 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324300 | TAGGCATCCCACTTC[A/G]AGATATTTATTCAAG | 286053 |
rs556513410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210945 | ACCATGTTGGCCAGG[C/G]TGGTCTTGGACCCCT | 286053 |
rs556513541 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258395 | TATGGTCTTATACTA[A/G]TAATCTGCACAGTTT | 286053 |
rs556542195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331761 | AACTTACTTTCTTTC[A/G]AATTTCAGTCAACGG | 286053 |
rs556556822 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289875 | AAAGCATTTATTATC[A/G]AAGCCTTTTTGTTTA | 286053 |
rs556558154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314612 | GCATTTTTAGACACT[A/C]GATCACTCCCTGAAA | 286053 |
rs556560788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323528 | TTTTCTACTCACATG[C/G]AAAGACAGTTCCATG | 286053 |
rs556573286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118627 | CACAGTTTAGGATTA[C/T]ATAAAAGATACAATC | 286053 |
rs556573490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358296 | CGAGATTGTGCCACT[A/G]CATTCCAACCTGGGC | 286053 |
rs556582211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365085 | GTGGGTGACTCACTG[A/T]TGTCTTTAGCTGCAG | 286053 |
rs556589358 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100829 | GCCTCCCAAAGTGCT[G/T]GGATTACAGGTGTGA | 286053 |
rs556590196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182623 | TGCTTTAAAATAACC[A/G]TACTTTGATTCTGGT | 286053 |
rs556623240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091390 | ACCAAGCAGCTGAAC[C/G]GTGCTTCCTAAAGCG | 286053 |
rs556626238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226309 | ATTTTAGAAATTCAC[C/G]AGGAAAGGAAGGTGA | 286053 |
rs556633472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227765 | AAATAAAAATCACCT[A/G]TAATCCCGTTACCCA | 286053 |
rs556641177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235921 | TAGTAGGTAAGAGTC[C/T]ACATTTTACATATAA | 286053 |
rs556642908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315839 | TCAGGGTTTCACTCC[A/G]TCACCCAGGCTGTTG | 286053 |
rs556644716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125099 | GCTAGGATTTTCTGC[A/G]TACAAGATCATGTCA | 286053 |
rs556650581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352728 | ATATTTTCTCTCCCA[C/T]CTTCCTTTTACCAGA | 286053 |
rs556676512 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277196 | TGCTGGTTTACTGAG[-/T]TTGAGGCTCTGTGAC | 286053 |
rs556677991 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109721 | ATTCCTAATTCCTAT[A/G]CCAGGTGTTTGTCCC | 286053 |
rs556681654 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366401 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGTGCCT | 286053 |
rs556694505 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365423 | ACCCTGCAGGATCCC[C/T]CATGCTATTTTCCCT | 286053 |
rs556705511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132633 | CAAGTAGCTGGGACT[A/G]CAGATACACGCTACC | 286053 |
rs556709905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125874 | TCCTACATTGGTGAG[A/G]AAGGGCCCAGGGTGA | 286053 |
rs556717149 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198548 | GAAGCCTACTTGATC[A/G]TGGTGGATAAGTTTT | 286053 |
rs556721232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294590 | TAGGGCTAAACTTGC[A/G]ATCGTATACTTTCTT | 286053 |
rs556738372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352231 | CACGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 286053 |
rs556755879 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364053 | GATTCAAGTGATTTT[A/C]CTGCCTCAGCCTCAC | 286053 |
rs556758324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286838 | AAACCTGGGACTTCA[A/G]CTCAGCTCTGGTTCC | 286053 |
rs556771116 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169291 | GCATCTATGCTCATA[A/G]CTTGAATTGCTGTCT | 286053 |
rs556771347 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265625 | CCTCTCAGGCAGGTG[A/G]CCGCCTTACTTTACC | 286053 |
rs556784566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301666 | CATTTTTTTTTTTTT[A/T]TTTTTTGAGACAGAG | 286053 |
rs556786507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098400 | CGAAGCTCTTTGGCC[A/G]TTACTCCCGGTGAGT | 286053 |
rs556792860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203706 | AAGTAATTGATGTCT[A/T]GGAGGTGAGAAGAAA | 286053 |
rs556816150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232972 | AACTGCATTGCAAAA[A/G]AATGGTCACATTCCA | 286053 |
rs556819646 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288991 | TTTATAGAGATGGTC[A/G]GTGTTGACCAGGCTG | 286053 |
rs556834386 | in-del | -/CT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135988 | CTTGCAGCCTGGAGG[-/CT]CTCTCAGGATACTAA | 286053 |
rs556834531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263535 | TGGGCAGATCACCTG[A/C]GGTCAGGAGTTTGAG | 286053 |
rs556836545 | snp | C/G/T | 0.00279258 | 0.0372817 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172278 | TGGCATATCTGTATT[C/G/T]TTGCTGCAGGGAAAG | 286053 |
rs556841069 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105079 | GCCATTGCAAGACTT[G/T]TCCCAGTTTTCCCTT | 286053 |
rs556849810 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260533 | GAACCTTTCACTTTC[C/G]TTCTCGGGGCCTGAG | 286053 |
rs556857540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191797 | CACATACATCATCTC[A/G]CGTAATCTTTACAAC | 286053 |
rs556868313 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276185 | ATAGCACCCCAGCCC[C/T]TGTACTGCCCAGGGC | 286053 |
rs556894065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322339 | TGCCACTGCACTGCA[A/G]TCTGAGAGTGAGTGA | 286053 |
rs556894234 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337654 | AATCCCAGCATGTTG[A/G]GAAGCCGAGGCTGGC | 286053 |
rs556905398 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241023 | TACCTGGGACCAGAA[C/G]TGTTTTGGATTTCAG | 286053 |
rs556939630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142930 | TAATTTTGCCACACT[A/G]ATATCTATGTGGAGG | 286053 |
rs556944187 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251130 | AAGCATAGTGGTTCC[A/G]TAATTTAAAAGTTTA | 286053 |
rs556961251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178045 | CTTCTAAAACAGCAT[C/T]CCAGTTGCCAGCCCC | 286053 |
rs556983809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360178 | CACTCTTATTGGAGG[A/G]TTGTGATAGACTCAG | 286053 |
rs556992517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204536 | GCATTAATTTTTCCC[C/T]GTACACAAAGTATTA | 286053 |
rs556994817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276776 | CCTGTTACAGACAAG[C/G]AAATGGAATCTCATA | 286053 |
rs557014904 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156322 | GTATATTGTTCTTTT[G/T]GTATGTGCTGCTTCT | 286053 |
rs557032890 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200845 | CTTGTCACATAGTCC[C/T]ATATTTCTTGGAGGC | 286053 |
rs557033530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099806 | CAGACGAGTTTTGCT[C/T]TAAGGCTGAGTAGAG | 286053 |
rs557045059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134374 | GAAAATATGGGATCT[A/G]TGTGTGGAGTATATT | 286053 |
rs557052233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270129 | ATGAAGTTGGAGACA[A/G]TATACAGGAGATAGA | 286053 |
rs557105838 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165973 | AGGTAAAGGATAAAG[A/C]GCATTAATAAACTGA | 286053 |
rs557110220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275959 | TTAGCCAATGTCTTA[A/G]AGTAGTCACTGGCAC | 286053 |
rs557124681 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222226 | GCCTTAAAGTAGGAA[C/T]GATTTTTTAAAATTT | 286053 |
rs557151750 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098971 | GCATACCACCTATAC[G/T]ACAGTTTTGGAGACA | 286053 |
rs557166616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219135 | TTTAAATGAACCATT[A/G]ATAATATACTCCACA | 286053 |
rs557167543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333306 | TCCCAAGTAGCTGGG[A/C]CTGCAGGCACATGCC | 286053 |
rs557176006 | snp | C/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125127892 | GAAGGTAATTTTATA[C/G]AACATTTTAAGTAAT | 286053 |
rs557184156 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252665 | GTAGTACATAAATGG[A/G]ACATCTTATAACTGA | 286053 |
rs557185387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347707 | AAAAGAGTGTGGGTA[C/T]AGACAGTGGATATTA | 286053 |
rs557187202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119697 | TTTTTGAGACATCAG[A/G]TTCCTTTTTAAAAGA | 286053 |
rs557194048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140564 | GCTACTCAGGAGGCT[A/G]AGGTTCAATCGCATG | 286053 |
rs557200046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248863 | TGCCCTAGGGCACTC[A/G]GGTATAATAATTGGC | 286053 |
rs557200192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256371 | AGGTGAAAGCTAGAT[G/T]CCAGTGCCACCAGAA | 286053 |
rs557209108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243044 | GGGTAAGCAATGTGG[A/G]AAAAAAATCACCAGA | 286053 |
rs557212508 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150437 | CTTTCTTTTTTTTTT[C/T]TTTTTTTTTTTTTTG | 286053 |
rs557239163 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308609 | GAGGGGAAATAAGTT[A/G]CCTGTTTAACTTCCA | 286053 |
rs557242096 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288288 | CTCTGACTGCTGGGA[C/T]GTAACAGGAGGCCCT | 286053 |
rs557246248 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120648 | TAGTTGCTATAAACA[A/G/T]TTAGGCCTGTCAGCA | 286053 |
rs557246444 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192400 | TGTGTTATTGTGTGT[A/G]TAGCAAGTAGACATG | 286053 |
rs557252013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338207 | TTCTGGTGCCCTTTC[C/T]ACCAAAGCACCATTT | 286053 |
rs557273122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354211 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 286053 |
rs557281467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166835 | CTATTCCATCTCCAT[G/T]CTCCTCCGAAGTCTT | 286053 |
rs557300603 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334445 | GAATTCAGAGAGCCT[A/G]GAAGGAGCATGGGGA | 286053 |
rs557321724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127353 | GTAAGGGCCATGTGT[A/G]TTTCTGTGTGGGGGG | 286053 |
rs557330769 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147956 | GTGGGAGTCCCTTCT[A/G]GTTCTCATCGTAGGT | 286053 |
rs557336963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249387 | GACAGTCCATTTGGA[G/T]CTTATAAGAATCCCT | 286053 |
rs557343556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340140 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 286053 |
rs557346930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357982 | GAAAAACAATACATG[A/G]GGGAAAAATTAGTAA | 286053 |
rs557364020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187222 | ATCTTAGATACTTCT[A/G]ATTCTTGGAGTCATA | 286053 |
rs557371877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193915 | CCATTAACTGTATGT[C/T]GTTGATTTATTTGCC | 286053 |
rs557400806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263851 | TCAGCTCTAGCGTGT[A/G]AAGAGAGATTTTTGT | 286053 |
rs557437540 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119675 | GATAGAACAGACTTT[A/G]GGATTATTTTTGAGA | 286053 |
rs557438552 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092989 | ACAAAGTCTACAGAT[A/G]CTGCTAAATGTCCCC | 286053 |
rs557439447 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304523 | GCCTGCCTGAAGGCA[A/G]TGGAGGTGCAGAGGA | 286053 |
rs557450341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283269 | TCAGGAGATCTGGGG[A/C]TAGGCATGGTGGCTC | 286053 |
rs557450380 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099276 | GGGTGGAGATTGGGA[A/G]GGCTTGCCGTTGTAT | 286053 |
rs557458589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332681 | AGAATGCTTTGTACA[C/T]TGCTATAGCAAGCTT | 286053 |
rs557473397 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325849 | CCCAGCTACTTGGTA[G/T]TCTGAAGCAAGAGAA | 286053 |
rs557508237 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200101 | CTCCTGAATACAGCA[C/T]ATTGTTGGGACTTGA | 286053 |
rs557524938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277387 | ATAATATGGTACTTT[C/T]CAGGACCTAAACAAT | 286053 |
rs557557031 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172988 | ATGGAGTTATTTCTA[G/T]CTTCCATTATCTTTC | 286053 |
rs557568506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309337 | TCAGTGTATAAAAAT[G/T]CATTAAGCACTTTAG | 286053 |
rs557572432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106133 | ACTAACCAAGTGACT[A/G]TTCTGCATATAATTC | 286053 |
rs557594070 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143874 | TGTAAAGGTAAAGAA[G/T]TTTTGTAGACCCATA | 286053 |
rs557599976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271783 | GCTTTTTAATGACTC[C/T]GTAATCATGTGTATG | 286053 |
rs557605724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234761 | TTCAATCATCTCTCT[C/T]AATGTAAACTTGGAG | 286053 |
rs557610573 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258936 | AGACAGAGTTTTGCT[C/G/T]TTGTTGCCCAGGCTG | 286053 |
rs557627373 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229655 | AGATGAAATTCAGTC[C/T]TATTCTCAAAATAGA | 286053 |
rs557633393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180153 | TTATGTAGAGGTAGA[A/G]GATAGCTAGTCACCG | 286053 |
rs557642382 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252455 | GGCGTGAACCCAGGA[A/G]GCGGAGCTCGCAGTG | 286053 |
rs557657079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136726 | TCACTCAACAAAGAG[G/T]TTTTTTGAGGCTTCT | 286053 |
rs557660007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129597 | GTGTGTTTCATTGAT[A/G]TTCTGAATACTGAGA | 286053 |
rs557662884 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091029 | GGAGCTCCATGCGCT[C/T]GCAATCAGGAGACCC | 286053 |
rs557668639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257227 | AGGCAGAGGTTGCAG[C/T]GAGCTGAGATTGTGT | 286053 |
rs557685538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171684 | CTCTTCTACCAGATT[C/T]TGTCTGGCTACATCT | 286053 |
rs557687917 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320078 | CTGCTCAGGAGGCTG[C/T]GGCAGGAAAATCGCT | 286053 |
rs557692643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237649 | CTGTGAATTAATAAA[A/G]TCACATTCTTTTTTT | 286053 |
rs557693876 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223281 | GAGGATTGCTTGAAC[A/C]CCAGAAGCAGAGGTT | 286053 |
rs557697251 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158903 | AATGCATTTTTCAGC[A/G]TGGAGTTGAAAGCAC | 286053 |
rs557704341 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268719 | AAGAGAAAGAGATGC[C/G]CTGGGAGGAATGGCC | 286053 |
rs557708296 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289809 | CAAATTCTGGTGTCT[C/T]CAGTTAGCAGTTGTT | 286053 |
rs557715378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107655 | TGCACCATTAGTACA[A/G]ACATTCAACATTTGT | 286053 |
rs557730915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215769 | GGTAGCCAGTTTTCC[C/G]AGCACCATTTATTAA | 286053 |
rs557735639 | in-del | -/AATT | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113015 | TATTTAATTTTTGTC[-/AATT]AAAAATAAATTTAAA | 286053 |
rs557746841 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298142 | GTACACACCTGTAGT[-/C]CCAGCTACTAGGGAG | 286053 |
rs557749194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319303 | AAATAAACAGCACCC[A/G]CAATGTCTAGATTCC | 286053 |
rs557765278 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115667 | GAGGCAGGAGAATTG[A/C]TAGAACCAGGTGGGT | 286053 |
rs557767917 | in-del | -/AAA | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359990 | TGGTTTAAGTTATAG[-/AAA]ATTAGAGTATAGAGA | 286053 |
rs557770535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187862 | TAAATGCTAAGCTTA[A/T]AGGAGAACGTATCAT | 286053 |
rs557771307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355632 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 286053 |
rs557810154 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107484 | GGCATGAGCCACCAG[A/G]CCTGGCCTATCAAGG | 286053 |
rs557817259 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351727 | AAAAATATTGTGGGG[C/T]TGGCCGGGCATGGTG | 286053 |
rs557820574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222217 | GATGTCATTGCCTTA[A/C]AGTAGGAACGATTTT | 286053 |
rs557828295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108368 | TTTAAGGAAATTGGA[A/G]GGTAGATCAGCCTGT | 286053 |
rs557829088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224133 | AAGCCACCATGCCCA[A/G]TCCTTTGCCCATTTT | 286053 |
rs557831921 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174418 | AGTTTCGTTTCTTTT[C/T]CACCAGTACGGGAAT | 286053 |
rs557840705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349808 | TCCTTTGTAATTACC[A/G]CACAGCCTACTGTAA | 286053 |
rs557844455 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332064 | ATATGAAGCCCACAG[C/T]CAGATATGAAAACTG | 286053 |
rs557851066 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213963 | TGTAATTCTTACTTT[A/C]TATCTGGATACTCTG | 286053 |
rs557851898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122793 | ATACTTTAGCATAAG[A/G]TATTCTCACCACTAG | 286053 |
rs557858761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123821 | TTTCACCTTGTTTTT[A/T]AAAAAAATTCCTCTC | 286053 |
rs557912685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188533 | TAGAAAACTCAGAAA[A/T]CTAAGTTACTAGATT | 286053 |
rs557912686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195745 | TATTTCTTTATAACT[C/G]TAAAACAAATATGCC | 286053 |
rs557930896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349297 | TGACCCCCAAATTTT[C/T]CAAGCACCAGCTCAG | 286053 |
rs557943198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317322 | CTCTCCCCAGCCTCC[A/G]AATAGCTGGGACTAC | 286053 |
rs557945364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357131 | CAGCAAATGCTCCCC[C/G]AGAAACTCTTCACCT | 286053 |
rs557956886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228911 | GAGTGATTCCCTCTA[A/C]GTTACAAAGCTTATA | 286053 |
rs557961292 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303002 | GTCCATGCTGCAGCT[C/G]CACACTCCCCGCATC | 286053 |
rs557964044 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312988 | AGTGAATTTGATGAT[C/T]AAGAGACAGTGAGTA | 286053 |
rs557964101 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323060 | GAGACTCTGTCTCAG[-/A]AAAAATATATGTATA | 286053 |
rs557966722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189022 | AAACATATTGAGTGC[A/G]TTTAAACTGGGCAAA | 286053 |
rs557972023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181730 | GTTGAGCATGAAGGA[C/T]GGAATAACCACTTGT | 286053 |
rs557978746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290786 | TCATGAGTTAGACAG[A/T]CAACTCCTACCACCA | 286053 |
rs557984424 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364141 | TAAAGATAGGGTTTC[G/T]CCATGTTGGCCAGGC | 286053 |
rs557995815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135900 | AGGTCCTTTGCATTT[C/T]CATGTGAATTTTAGA | 286053 |
rs557996388 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355104 | CAAAGTCCGAAATCC[A/G]AAACACTTCTGGTCC | 286053 |
rs558001490 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264551 | ACCTGGGACCATCTG[C/T]GCGCACCACCACGCC | 286053 |
rs558002174 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134213 | ACAGAAAAACTGTAA[C/T]GAGGACACCCAGACA | 286053 |
rs558005503 | in-del | -/T | 0.0741063 | 0.177655 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207154 | GATGGAATTCACCAG[-/T]TTTTTTTTTTCTCTG | 286053 |
rs558021888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327866 | GGGTTTACAGAGATT[C/G]TTGACATCTCTAAAT | 286053 |
rs558023360 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298279 | TAAATAAATAAAATA[A/G]TGCTGACTACATGCC | 286053 |
rs558025332 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148853 | AATCAATTTACTGAA[A/G]TGTAACTAAGTACAG | 286053 |
rs558026459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094147 | ATATTGGGTATGAAG[G/T]GGAGAAGGAAACAGG | 286053 |
rs558037129 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117334 | TCAAGCAATTCTCAC[A/G]CCTCAGCCTCCCAAA | 286053 |
rs558039798 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151631 | TACAATTGAGACCAG[A/G]TTTAGTTACTCATTC | 286053 |
rs558041281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361889 | ATAGACCTTCTGTCT[A/G]TAGCTTGTAGACTAA | 286053 |
rs558042296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195375 | CTAGGCGCTCTAAAC[A/G]ATACAAATCTGACAC | 286053 |
rs558052842 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215787 | CACCATTTATTAAAT[C/T]GGGTTCTATCTCTAT | 286053 |
rs558057764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355186 | ACCTCATCTGGCCTA[A/G]GTGATGGCCCACAGT | 286053 |
rs558080470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318397 | TGGGCGACACAGTGA[C/G]ACCCTGACTCAAAAA | 286053 |
rs558083172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248652 | AGCAAGACTCCATCT[C/G]AAAAAAAAAAAGTCA | 286053 |
rs558085487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342558 | TGTTCTACGATGCTG[A/G]CTCAGTGATGCCTTC | 286053 |
rs558086763 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152658 | AATAGCACAGTGTAT[A/G]TTACAGATAAGAAAA | 286053 |
rs558094383 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232650 | AGTAGAATGTTCTGC[A/G]TACTCATCCCCACCT | 286053 |
rs558097613 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113820 | GTAATCTCTCATGAA[C/T]GCTTTTGCCCATTGG | 286053 |
rs558109360 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271610 | ATCTTTGAAACCAGT[A/G]ATGAAATGGCTTTTG | 286053 |
rs558109760 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206831 | GAGGGGGAGAAAGGC[G/T]TTTCACTTGCTTCCA | 286053 |
rs558120047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201339 | TTTGATGTTGGTGAC[C/T]TACAGATGGGGTTTT | 286053 |
rs558131117 | snp | A/G | 0.0349115 | 0.127424 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363563 | GAGAGAGAGAGAGAG[A/G]GAGGGAGGGGGAGGA | 286053 |
rs558146382 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248008 | GTATGTTAGATTTTC[A/G]AATCTGTAGAGAAAA | 286053 |
rs558154804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151869 | TAAGAAATGAGCAAT[A/G]CGATTGCAGTCATGT | 286053 |
rs558170921 | in-del | -/TTTG | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231422 | AAGCATCTGAAGACC[-/TTTG]TTTGAGTTCTGCCAC | 286053 |
rs558211253 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167771 | TTGTAAGATTTTTTT[A/T]TTTTATTTTAGGAAA | 286053 |
rs558220107 | snp | C/G | 0.000891663 | 0.0210959 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242106 | TGTAAACAATAACTG[C/G]GGGGGGAGTTTGAGA | 286053 |
rs558243175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198056 | TCCTGAGACTTTGCC[A/G]AAGTTGCTTATCAGC | 286053 |
rs558250121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266934 | TTTATTTATAAATAA[A/C]GGTAATCTGAACATT | 286053 |
rs558287729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336647 | ACATGGTTGGGTTCA[C/T]AGTTTCATCTGCCAT | 286053 |
rs558290506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102185 | TCTTCTCTATAGGAT[A/T]TACAGAATAGTGTGG | 286053 |
rs558295423 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244811 | TGCTGCAATTTGGAC[-/T]TTTTTTTTCAGAGTA | 286053 |
rs558296449 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145392 | GTGGGGTGGCAGTGC[-/G]GGGGGGGATAGCTAG | 286053 |
rs558309752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117724 | TCTTGCTATGTTGCC[C/T]AGGCTAGTCACAAAC | 286053 |
rs558310065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110732 | AATGACATTTAGCGA[C/T]GTTTTGCTTAGATAA | 286053 |
rs558311152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138818 | CTGGAAGAGACTTGA[C/G]ACTTTCTGTTTGACC | 286053 |
rs558311518 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266308 | GTTGGTCAGGCTGAG[A/G]TCTATTTTTTAAACC | 286053 |
rs558312464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140400 | AGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 286053 |
rs558313702 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351122 | GGCTTTGAGCAACTC[A/G]GTGGATGCTGACTGA | 286053 |
rs558317373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272804 | ACATGTGTATATATA[C/T]ACACACACGTATATA | 286053 |
rs558329187 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203951 | TCAGTTTACTTTCCT[A/G]TGGGATTCCCTAGTC | 286053 |
rs558350246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334049 | AACAGACAAAGTTGT[A/C]TGTGTCTGTACTTTC | 286053 |
rs558373560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111267 | TTACTGCCCTCATGA[A/G]TAACTGACCTTTTAC | 286053 |
rs558378608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094915 | CTGGAGTGCAGTGGC[A/G]TGATCATGGCTTACT | 286053 |
rs558379132 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233004 | GGTTGTAACTAGTTC[A/G/T]GGAGGCTTAGTTACG | 286053 |
rs558386153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116571 | GTTGCTCTGTGTGTG[C/T]GTGTGTGTGTGCGTA | 286053 |
rs558386416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145346 | TTTATAATGTAAATC[A/G]GGGATTATCTGTGCC | 286053 |
rs558392732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252841 | TAGATGGGTAGTTCC[A/G]GAGTTAAGAGCGCAA | 286053 |
rs558394296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216354 | TGAATCAAATGATCT[G/T]TGGGTCCGGGCGCGA | 286053 |
rs558402289 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224228 | GCTCATTATCACATG[C/T]ATGCTTCGCAAATTT | 286053 |
rs558430473 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159493 | CTAGGAGTAATAGGC[-/T]TACTATAGAGCCCAG | 286053 |
rs558445611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117089 | GAGCTTCATCAGATT[C/T]GCTTTTTTCTTGATT | 286053 |
rs558463156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202304 | TTCTGCGTCGATCAC[G/T]CTGGGAGCTGCAGAC | 286053 |
rs558466392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343811 | CCATCCTGGCTAATT[C/T]GGTGAAACCCCGTCT | 286053 |
rs558468294 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351530 | CATTGGTCACAAGTT[G/T]GACAGCCGGCATATG | 286053 |
rs558475143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163729 | ACTTCCTGATTCTAC[C/T]AACAAGAATGGGAAG | 286053 |
rs558486879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096457 | TTTTTTTCAGTGTAA[C/T]CCATTATCTCATATA | 286053 |
rs558492453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109215 | TCTTATCTTTGTGAC[C/T]TTGGGCAAATTCTCT | 286053 |
rs558494762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153858 | AACCCCTTAGAGAGA[C/T]GGAACAAAATCTTCT | 286053 |
rs558503957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103296 | GGACAACAGAGCAAG[A/G]CTCTGTCTCAAAAAA | 286053 |
rs558532361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262707 | CTAGTTTTTTTTTCT[A/G]AAAACTCACTGGTAG | 286053 |
rs558555765 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343658 | TTAAAAAAAAAAATT[A/G]AAGTATGACATATAA | 286053 |
rs558575080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202981 | TAGGAAGACAGAAAC[A/T]GAAGTGTCAGGAATT | 286053 |
rs558606997 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154440 | TGTCTCTCAAGAAAA[C/G]AGGGCTACTATACTC | 286053 |
rs558616655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163104 | AGGCTTGGTGGCTCA[C/T]ACTTGTAATCCCAAC | 286053 |
rs558621700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253951 | TCATCATGACTTCTC[C/T]TATAAGATTATCCTA | 286053 |
rs558623210 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142425 | TCTCTTCTGTGTCAC[A/G]ATGATGAGGGAATTG | 286053 |
rs558624041 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191420 | CTTGGAAAAAAAAAA[A/T]TGACTTTTAATAGGA | 286053 |
rs558629081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262999 | TTTATGCTGGTCAGT[C/G]TTACCATTTCCTCCA | 286053 |
rs558634389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293422 | TGTGGTGCTGACCAG[C/T]TTTCCCCATATAGAG | 286053 |
rs558636436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196732 | AGTAATGGGATCGCT[A/G]GGTCAAATGGTATTT | 286053 |
rs558639698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103810 | TAATTGTTGAAGACA[C/T]AACAAAGAATTAAGT | 286053 |
rs558647551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253199 | GGAAGTTTATATACA[C/T]TTAAGGGAGCTACCT | 286053 |
rs558666162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146954 | GCCCTGAGATTTGAT[A/G]TAAGTTTGATGTGCT | 286053 |
rs558688304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306754 | GTAATGGTTAAAAGT[A/G]CAGGTCCTGGAGCTG | 286053 |
rs558715181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301299 | GACAGCAAACAGCGT[C/G]CCAAGTAGTCATCTA | 286053 |
rs558718540 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171304 | GCTGTGTTCCCAGCT[-/C]CTGGAGCAGTGTGTG | 286053 |
rs558721646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365584 | TCCAAGTCCAGGCAC[A/G]GTGGCTCATGCCTGT | 286053 |
rs558736572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168848 | AAACAGAAGATATGT[A/G]GTAATAAGAATGAAG | 286053 |
rs558746617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161304 | GGACTTCCTTTTTTA[A/T]AAAAAAAGTCTAATA | 286053 |
rs558754648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170113 | CTGTAACCTAGTCCT[C/T]TCTCCAAAACCACAT | 286053 |
rs558755139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299598 | CATGTGGGGACTACA[A/G]TTTGAGATGAGATTT | 286053 |
rs558769929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124553 | GGGTGATCAACAGCT[C/T]ACTGTAGCCTCAACC | 286053 |
rs558772318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170798 | TCCATGCCATCATCA[A/C]TTTTTACCTGGATGC | 286053 |
rs558797549 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140468 | AGGAGTTTGAGACCA[G/T]CCTGGCCAACATGGT | 286053 |
rs558809341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203882 | ATAACTTGTTAGCTT[A/G]AAAGTAGGAGAAAAA | 286053 |
rs558811966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161997 | TACCACGAAGCAAGT[C/T]CTCTCTACCCATCAG | 286053 |
rs558834862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366276 | CTGGGCGCGGTGGCT[C/T]ACGCCGGTAATCCCA | 286053 |
rs558850046 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268374 | CGTTTGAAGGAGAAA[A/G]AAGTTAAAAAAAAGA | 286053 |
rs558855591 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261096 | GGGGAGAAAATTACT[G/T]TTTTGCGAATCAACC | 286053 |
rs558856354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133751 | ACAAAGCAACAGAGC[A/G]AGACTCCATCTCAAA | 286053 |
rs558883999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301816 | TATAGGCACCAACCA[A/G]CCATGCCCGGCTAAT | 286053 |
rs558901993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292371 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 286053 |
rs558926821 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211215 | AGGTGATACATGCAC[A/G]TAGTACAAACTTCAC | 286053 |
rs558933059 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156445 | TAAAGCATTTATATT[A/G]GATTACAGCTACATA | 286053 |
rs558954269 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311869 | AGATTACCTGAGGTT[A/G]AGAGTTCGAGACCAG | 286053 |
rs558967884 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118760 | ATTTTTAGATCAACT[A/C]TTCCAGGAATGAGGA | 286053 |
rs558990884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249512 | CACTTTGAAAAAATT[C/T]TGGGCAAAACATTTC | 286053 |
rs558991373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176529 | TTTCCATTAAAATCC[A/C]TACACTGGTTGCTCC | 286053 |
rs558991524 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132420 | TCAGCTCTCTAGGAA[A/G]CAGTGTGATAGCAGT | 286053 |
rs558996191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211423 | TGAATATTCCATATC[A/C]GTACATATAGCACTG | 286053 |
rs559016217 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183459 | CTAATGTATTTTTCA[C/G]TCTTCCCTCAAATGA | 286053 |
rs559023445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105220 | CAGTTATTCATTTAC[A/G]GCTAACAGCAGGTGT | 286053 |
rs559032039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346500 | TCAGACTTTACTGAG[G/T]ATGTAAATAATGGAA | 286053 |
rs559071737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226358 | ATAAATTCTAATCAT[A/G]GGACATTCGCGTGGG | 286053 |
rs559075701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177141 | TAAAGTCTCTATGCT[A/G]AAGTTAGAAGGAAAA | 286053 |
rs559104399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274568 | TTTATTTGCCTATTT[A/C]GGTCATTATTTTCTA | 286053 |
rs559119783 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250011 | TATTTATTTTTGAGA[C/T]GGAGTTTCGCTCTTG | 286053 |
rs559125868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322995 | ACCCAGGTTTCGGAG[A/G]TTGCAGTGAGCCAAG | 286053 |
rs559175055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191821 | TTACAACATCCACAC[A/G]CAGGAAAGGAATGCA | 286053 |
rs559175485 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302636 | CTTCTTAATCAGATA[C/G]AACAAGAAGATTAGA | 286053 |
rs559178714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359213 | CGGAGCTTGCAGTGA[A/G]CCGAGATCATGCCAC | 286053 |
rs559189644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171126 | GTCGTCTTTTCATTG[A/C]AGCCTGCCTTGACCG | 286053 |
rs559202012 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159418 | TAGATACATAAATAG[C/T]TGTCATGTTACAGTT | 286053 |
rs559213036 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322475 | AGAAGGGAACTTCTT[A/G]AATCTACTAATGAGC | 286053 |
rs559276259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090158 | CTAGACCTCCTAACC[C/T]GGACTAGTTATATTT | 286053 |
rs559288315 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314396 | CCAGATTCAAGCGAT[C/T]CTCCTGCCTCAGCCT | 286053 |
rs559293907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217735 | CTGTCACTGTGCTCA[A/G]TCCTGTTATTACAGC | 286053 |
rs559294744 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280321 | TCAGAGAGAGATTCC[A/T]TAAATTCAGCAACTG | 286053 |
rs559299125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353182 | TCTGTTATTCATCCA[A/G]CAGATTTTCTGGTGA | 286053 |
rs559308060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270430 | AGATCGCACCACTGC[A/G]CTCTGGCCTGGGTGA | 286053 |
rs559318851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308983 | GGCACGGTGGCTTAC[A/G]CCTGTAATCCCAGCA | 286053 |
rs559325799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178121 | CTCAGTTGTGTGTCC[A/T]CCAGGCATTAACAAT | 286053 |
rs559334483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128491 | AAATTTCTGACATAC[A/G]CATCTATGTTAATGG | 286053 |
rs559350239 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367419 | ACTCGGGAGGCTGAG[A/G]CAGGAGAATCACTTG | 286053 |
rs559350314 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354520 | TTTTGAAGCCAACCA[A/G]TGGTTTTTAAGGTCT | 286053 |
rs559359088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164243 | GAAAGGTGGCTATTG[C/T]TGACTCTGAGCCTCA | 286053 |
rs559363674 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249816 | TTGGGATGATGGTGA[C/T]CATTATTATTATTAT | 286053 |
rs559369867 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119155 | CTGCTGTTCACCTCA[C/T]CTCACCTCCTGTTAC | 286053 |
rs559382602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264236 | TTGACATTTCTTTTT[C/T]AATCTTAGCATTTCT | 286053 |
rs559382950 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191124 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGCACT | 286053 |
rs559408958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090891 | ATTTTCCAGAAAAGT[C/T]CTGAAATGAGGCTGA | 286053 |
rs559423678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156709 | TACTTGATGTATGCT[A/G]TTGAAACCAAAGCAA | 286053 |
rs559426573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256788 | AAATCAGCTGGGCGT[A/G]GTGGCACATGCCTGT | 286053 |
rs559429623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323596 | AGGACAGCCTTTGCA[A/G]CAAATGGTTCTGTAA | 286053 |
rs559448966 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199453 | CCCAGTAGTCATTCA[-/G]GAGCAAGTTGTTCAG | 286053 |
rs559450987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226747 | GGTAGAAGCAGGGAA[A/G]TAAGCATGAATAAAG | 286053 |
rs559459890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179657 | TGCTTTACAGCAGTT[C/T]TCTAAAAGTTCTGGT | 286053 |
rs559462429 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276857 | CCAAATGCCATCTCT[C/T]CTGGAAAGCCTTTTA | 286053 |
rs559469775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127625 | CAGAGTTCTTGGGTC[C/G]TTCTGGAGTTTGTTG | 286053 |
rs559473555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262057 | AATTGAGATTGCACC[A/G]CTGCACTCCAGCCTG | 286053 |
rs559477836 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301585 | AAGGGGACCCAGGCA[C/T]GGTGTCAGGACCTCT | 286053 |
rs559479203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295062 | AGGTTGGACTTTCTT[A/G]AATGTCGTGTTGCTG | 286053 |
rs559479379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177453 | TCCTTTGCCATCAAA[C/G]TATATTCATTGGTTC | 286053 |
rs559487498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274884 | GCAGTGAGCCAAGAT[C/T]GCGCCATTGCACTCC | 286053 |
rs559495634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163508 | GTAACTTCTGTATTT[C/T]AGCTTCCTCATTTCT | 286053 |
rs559506288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126283 | AGGCCGAGGCAGGAG[A/C]ATCACTTCAACCCAG | 286053 |
rs559514057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234474 | TCTGAATCTTTCTTG[C/G]TCTGTAATACATTTC | 286053 |
rs559541116 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170468 | TGGAGTGCAAATGGC[A/G]CTGTCTCGGCTCACT | 286053 |
rs559541725 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362665 | CAGAGTGACACAGCC[-/A]GGGGGTTTAAGCCCA | 286053 |
rs559543049 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326792 | AAAACACCATCTCTA[C/T]TAAAAACACAAAAAT | 286053 |
rs559545527 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329844 | CACACAGTGTTCACT[A/C]AGTTCAAGGCCTGGT | 286053 |
rs559547976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366004 | CTGGAACGTCCTCAG[C/T]ACTGCACTTGCTACT | 286053 |
rs559576009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113414 | AAGCCCAGGAGTTCA[A/G]GGCTACAGCAAGATA | 286053 |
rs559583788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220958 | ACTTGGGCCCTGTGT[A/G]TGCTAAAAATATCTC | 286053 |
rs559598329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244406 | TTCTTAACCTATATG[A/G]CTAAGGGAGGGGGAA | 286053 |
rs559600004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134483 | ATATGCAATGGTATC[G/T]TATAGTGGTTTTAAT | 286053 |
rs559600506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236353 | TTAAATGTAAAAGGA[C/T]GAGTTGCAAAACTAT | 286053 |
rs559606603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326965 | CCATTTCAAAAAAAA[A/G]AAGAGAGAGAGAGAG | 286053 |
rs559615095 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271016 | CCTATAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 286053 |
rs559638001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269510 | CTCCTCTGTATTCTG[C/G]TCACTGCTTGATCAA | 286053 |
rs559638404 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186008 | CTCACTTTGACAACT[C/G/T]TAGATCTAGGCCTGG | 286053 |
rs559640419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106249 | CATATTAAAATACTA[A/C]AACAATGAGAAAACA | 286053 |
rs559653403 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219954 | AGGCATACAACGTAG[C/T]CTGCCTTATGGTTAA | 286053 |
rs559662810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243890 | AAGAGCAACAGGAAG[A/T]TCATCTTTGTCACTG | 286053 |
rs559672364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140759 | CTGTTTCTTAAGCCT[C/T]TTGGGTTTCCAAGTC | 286053 |
rs559675079 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187655 | ATCAGGCCCTGTAGA[C/T]TTTAGTGTACATCAG | 286053 |
rs559683664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099357 | CCTTAGAGAAGTAAG[A/G]GAATTGACCTAGTAG | 286053 |
rs559684723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283970 | CATCCTGGCTAACAT[A/G]GTGAAACCCCGTCTC | 286053 |
rs559698174 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268675 | AAACAAAAGAGAGAG[C/G]TGAGATGCACATACA | 286053 |
rs559704488 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350032 | ACTCCTGCCTTGTTG[A/G]ATGAGGCACTTTGCT | 286053 |
rs559712628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228362 | AGAAAAGTATGCTTT[C/T]TGCCTTCTAGAAGCT | 286053 |
rs559715821 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142589 | TTTCTAGTGGGCGGC[A/G]GTTATAAAATGTGTA | 286053 |
rs559723785 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295849 | TTTTGAGCATTCTAT[C/T]GACTAAAATATTATT | 286053 |
rs559727401 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092153 | ATCCTTTCGCCTCAA[A/G]TGTGTAGGGGCAAGA | 286053 |
rs559743481 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290314 | AGCGGTAGCAAAAAA[A/C]AATTAATAAATAGAA | 286053 |
rs559748262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271571 | AAAGGCTGATTCAGT[C/G]CCTGACATGACTCCT | 286053 |
rs559760271 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338950 | TCTGCCCTAGATTTA[A/C]AGTTGACATGAAGGT | 286053 |
rs559764219 | in-del | -/AATA | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093534 | CTCTACTAAAAATAC[-/AATA]AATAAATAAATAAAT | 286053 |
rs559764885 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272565 | TATGACATCATTTCC[A/G]CTAACAGACCAGTCA | 286053 |
rs559781300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143118 | CACACACACACACAC[A/G]CACAGAGGTAGGTGC | 286053 |
rs559818201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199719 | GAGCTGAGTTCAAGT[C/G]CTGGATATCCTTGTT | 286053 |
rs559823597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283329 | TTAAGTGGGTGATCA[C/G]TTGAGTCCAGGAGTT | 286053 |
rs559840607 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352576 | AAATAGAACAACACA[C/T]TGATTTATTAAATTC | 286053 |
rs559855230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272184 | ATGCCTGTCGAATTT[G/T]TTTGTATTTTTAGTA | 286053 |
rs559904605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264610 | TGGGGTGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 286053 |
rs559947616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241999 | AGACCAAAGATCCCT[A/C]GATGTGAGAACTGCT | 286053 |
rs559947622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158971 | TTTCAGTTATCTGTG[A/G]CCATCTCTGGTCCAA | 286053 |
rs559954100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327049 | AGGTGGATCACCTGA[A/G]GTCAGGAGTTCCACA | 286053 |
rs559969038 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237408 | TAATGTCACTGTTAC[A/G]GTTCCTAACAAAGCA | 286053 |
rs559972975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193487 | ATTCATAGAATAAAC[A/G]CTGCTGGTTGTAGCA | 286053 |
rs559995324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282843 | TAACACAGTGTACAG[C/T]CCTACTGGGCAGTTC | 286053 |
rs560008553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165902 | GGAGCCATATTAATT[A/T]TAGAGAAAGCAGTGC | 286053 |
rs560011742 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317866 | ACCAGAATGCCAGTT[A/T]AATTTTTAAAAAGTT | 286053 |
rs560013384 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147509 | GATATCAAGAGTGTA[C/T]GTGTTAAGGCAAATT | 286053 |
rs560042265 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258529 | CATAGGAAAGCAGCC[G/T]CAGCCTGGACAAAAG | 286053 |
rs560043472 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332130 | CAGGAGTTGTACTCT[A/G]AATTTTATTTATTAT | 286053 |
rs560044466 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276771 | TTATTCCTGTTACAG[A/G]CAAGCAAATGGAATC | 286053 |
rs560045366 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303965 | TAAAAGAAATCCTGG[C/T]TGTGTTTGACCTTTC | 286053 |
rs560051788 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293778 | CTATCTGATGTGCTA[A/C]TATTCTTCTTTATAA | 286053 |
rs560084463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157518 | ATTAACTTCTATTTC[A/G]GTGGTTTAGAACTCC | 286053 |
rs560111901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192935 | TGGAATTCCATACTT[G/T]AAGGAGATGTTCTGA | 286053 |
rs560116002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144585 | CTCTTAGTCACAAAG[A/G]ACCTGGAATTGGTCT | 286053 |
rs560122512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094363 | TTGTACTTAGCTGTA[C/T]TTATTGGGAGAGATT | 286053 |
rs560127406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305485 | TAGTTCTGGAAGCGT[A/T]AAACTGTCAGGCAGA | 286053 |
rs560135303 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143167 | CTAGAGATAGTTGGA[A/G]CTATAGTTTCAGAGA | 286053 |
rs560159051 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258959 | CCAGGCTGTAGTGCA[A/G]TGGCACGATCTCGGC | 286053 |
rs560161301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121649 | CTGATTCTGTATCCC[A/G]TAGGCATACATCTTT | 286053 |
rs560177132 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333704 | AGTTTTAGTAGAGAC[A/G]GGGTTTCACCATTTT | 286053 |
rs560183073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101747 | GATGTGCTGCCAGAA[A/G]ACAAGTTTATACAGA | 286053 |
rs560213960 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320995 | AAGAGAGAGGGGCTA[C/T]GCACTTTTCAACCAC | 286053 |
rs560216662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201486 | AGACCTTGTTTGCCT[G/T]GGTATCACCAGCGGA | 286053 |
rs560223516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114563 | GATTTTGCCCTCCAG[A/G]GTTCCTTTGGCAGTG | 286053 |
rs560238603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299130 | TAAACCTTTGAAGTA[C/T]TTTTATAGCATCACC | 286053 |
rs560242562 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326666 | TGGTTAAAAAGATAA[A/T]AAAGGCGGGCCAGGC | 286053 |
rs560249954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107775 | CTGGTGGCTGACACC[C/T]ATAATCCCAGCACTT | 286053 |
rs560250904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296806 | AACTCAAGGCTGGGC[A/C]TTCCTGCAGGAAAAT | 286053 |
rs560254188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343078 | ATGCATGTAAAAAGG[A/G]AAAACAAGCATGTTT | 286053 |
rs560256782 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340160 | GCTGGGACTACAGGC[G/T]CCCGCCATCACGCCC | 286053 |
rs560263330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166327 | GCTGGAGTGCAGTGG[C/T]GCGATCTCAGCTTAC | 286053 |
rs560276242 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347498 | TCTCCTACCAGACCC[A/G]ATCTTATTCCTCTTT | 286053 |
rs560277872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141178 | TAGATATTAACATAC[A/G]TTCTAAGGATATATC | 286053 |
rs560292612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101193 | TGACATGGTAGGTAC[C/T]CAATACTTATGAGTG | 286053 |
rs560293884 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257823 | ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCAGACA | 286053 |
rs560297343 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118071 | AGCTTGCTGGGCCAG[G/T]CATGGAGAAGGGTCA | 286053 |
rs560308374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303537 | TGTGCGAAGTATAAT[A/G]CTGGGTGCCAAGAAC | 286053 |
rs560339468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334260 | GCCTCACTGGAGGTG[A/C]TTTGATCATTGTCAT | 286053 |
rs560358404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115948 | CCTCACTCCACAGAA[A/G]GGGAAATTAGGCTCA | 286053 |
rs560375020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291991 | TCCCGCACTCAATTC[A/C]TTCAAGCTGGTCCAT | 286053 |
rs560386511 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107003 | TCTGTCTCAAAAAAA[A/C]AACAACAAAAAAAAA | 286053 |
rs560386679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206988 | AAAGGGAGAAAGTTT[G/T]TCTTCTTAGTATCAT | 286053 |
rs560392039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312508 | CACACGCCTGTAGTC[A/C]CAGGTACTTGGGAGG | 286053 |
rs560415895 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253218 | AGGGAGCTACCTGTT[C/T]CCTTCTCTTGAAGGA | 286053 |
rs560436245 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222764 | TTTAAATCTGTTCAT[A/C]GATGAGAGACTCTTA | 286053 |
rs560451337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311925 | AATACAAAATTAGCC[A/G]GGCATGGTGGCGCAT | 286053 |
rs560452570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173925 | CTCATATCTGTGAAA[C/T]TGGGATAATGATATT | 286053 |
rs560458987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341346 | TTTCCTGTAGAGTTC[A/G]TAAAGCAAGTTCTGA | 286053 |
rs560473939 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206293 | TAAGTTGGGACAGAT[G/T]TATGGAGTTACTTGT | 286053 |
rs560474153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214220 | ACTGTATCAAGGTTT[A/G]GAATACCAAGGGTCA | 286053 |
rs560482776 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233912 | CCGGGCATGGTGGCT[C/T]ATGCCTGTAATCCCA | 286053 |
rs560488861 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202344 | TCCTATTCAGCCATC[-/T]TGGAACGGACCAGCC | 286053 |
rs560495079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153184 | AACAACATTTCTTTC[A/G]TCTTGAGGTTTCATC | 286053 |
rs560516691 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107931 | CCCAGCTACTCAGAA[G/T]GCTGAGATGGGAGGA | 286053 |
rs560517761 | snp | C/T | 1.64866e-05 | 0.00287106 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125357244 | AGCTGACAGAGAAGC[C/T]GACGGAACAGAAGGA | 286053 |
rs560519321 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242775 | AGAGTCCCCCACTCA[A/C]AGCACAAACGCATAC | 286053 |
rs560529810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123307 | CCTCCTTTCCAAAAG[C/T]CCTTTACATTTTCTG | 286053 |
rs560536426 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268691 | TGAGATGCACATACA[-/C]CCATTGCCTAGAAAG | 286053 |
rs560536536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110115 | AAATGTTAATGTACC[A/T]CAAAGATGTAAACTA | 286053 |
rs560555487 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226724 | AGGCAGAGGGGATGT[A/G]GAAAAGAGGTAGAAG | 286053 |
rs560561819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125318 | CTCCCTTCCTCCTGC[A/T]GTGGCCTTCTAACGC | 286053 |
rs560568278 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262031 | GAACCCAGGAGGTGG[A/G]GGTTGCAGTGAATTG | 286053 |
rs560591596 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228678 | TGAATGTCCCAGAGA[A/G]TCTGGTGTGTTACAT | 286053 |
rs560604823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260598 | CGTCTTCTTTGTGGT[C/T]TAATTCCCTAATTTC | 286053 |
rs560609965 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261766 | AAAAAAAACAAAAAC[A/G]AAACAGCTTAGAAGC | 286053 |
rs560615772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132098 | TCATATTCTTCTTCT[C/T]CTTATGGGGAGTTGG | 286053 |
rs560621774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232032 | ACCCACTGTATCTCA[C/G]AGTATCATCTTGAAC | 286053 |
rs560622802 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299703 | ATTGGGAGGTTGGCA[A/G]TTCATTTCACTGAGA | 286053 |
rs560629865 | in-del | -/GATTT | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117085 | AGCAGAGCTTCATCA[-/GATTT]GCTTTTTTCTTGATT | 286053 |
rs560630599 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137456 | GTGTAGAGATATGCT[A/G]ATCTAAGGCAGTTGC | 286053 |
rs560630758 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167838 | AGTTTTCTCAGTTCC[A/G]CATGCTGTGATGTCT | 286053 |
rs560630972 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286368 | CCCAGGCTGGAGTGC[A/G]ATGGTGCAGTCTCGG | 286053 |
rs560645842 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181776 | TGAGCAGACTTGGGT[-/G]GGTGATGCTCAGGTC | 286053 |
rs560655485 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174769 | AACACCTTGGCAAAC[C/T]GTGAAGTCCACTTGA | 286053 |
rs560661893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363018 | AGGCCTTTGCTGGGT[A/G]GAATGGAAGAGACCA | 286053 |
rs560675936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351188 | TCCCTGAGTCATAAC[C/T]GACAAGCCACAAAAA | 286053 |
rs560677250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124822 | TTTTTTGAGACAGAG[A/T]CTTACTCTTTTGCCC | 286053 |
rs560678553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131193 | TATTATTTTTGGATA[C/T]ATTATAATTCTTTGT | 286053 |
rs560686517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231552 | TGGTCATTCCTACCA[C/T]AGCACTTTTGCACAC | 286053 |
rs560697572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132964 | TCTCTCTTAAAAGTA[A/G]GGAAACTGAGCACCA | 286053 |
rs560708131 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314767 | ATTCAATCTCTTTTC[A/G]TTCATTCATTGTGCA | 286053 |
rs560734071 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361989 | CAAGGTTCCCCACAG[C/G]TCTGTGGGACCCCAA | 286053 |
rs560761023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328014 | ATTATGGGTGAGGTT[G/T]TCTAGCACAAGGAAA | 286053 |
rs560762461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336105 | CCACTCCTGGTAGAA[A/G]GGAACCATTGATATG | 286053 |
rs560769010 | in-del | -/AAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313227 | AAGAAAAGAAAGAAA[-/AAG]AAGAAAGAAAGAAAG | 286053 |
rs560769244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174635 | GGTCTATTCAAACTA[G/T]ACAAATAACATTCTT | 286053 |
rs560782207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268454 | CATTAACAACAACAA[C/T]AACAAGCAAAAAGAA | 286053 |
rs560803760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140068 | AACCTCACAGCAATG[G/T]TTGCCTCTAAGGAGA | 286053 |
rs560807112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202321 | TGGGAGCTGCAGACC[A/G]GAGCTGTTCCTATTC | 286053 |
rs560814834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130629 | CTGCTACCAGAAAGT[A/G]ACTGCCTCTAAGCCC | 286053 |
rs560815076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102758 | CCCAAGGAGCATACA[A/G]TCTAAAGTATTTGAC | 286053 |
rs560820542 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302839 | TTAGCCTCCACTTGA[C/G]CACTCTGCAAGACCA | 286053 |
rs560830816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223421 | CCATATCTTGACTAT[C/T]GCGAATAATGCTGCA | 286053 |
rs560832961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233073 | TTACGGAAAAGTAAG[A/G]AATCTGAAGCGTGGC | 286053 |
rs560844874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356081 | TCTTTTCATGAGTGA[A/T]TTTTCCCAGAGACTA | 286053 |
rs560853281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272412 | TTATTCAAAAATCTC[A/G]GCATTTAGATCTAGA | 286053 |
rs560869585 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154003 | TTGCACAAGGTGTTC[A/G]TGGCCTCTGAAATGA | 286053 |
rs560878724 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283980 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 286053 |
rs560879873 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319524 | TACATGGAAGGTAGG[G/T]GTGTGTGTGTGGGCA | 286053 |
rs560894666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240503 | CACATACTGGCAGCA[C/T]AGGGACCTTGTATAA | 286053 |
rs560896022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225791 | AGTTTTCACTTCAAG[C/T]ATCATTGCTTTTGGC | 286053 |
rs560914984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281409 | ACATTATACAGCAAG[A/G]TTGCCAGAGGAGATC | 286053 |
rs560940498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314924 | TGTTGGGTGGAATGG[A/G]AGCAACTAATTCCAG | 286053 |
rs560942464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307175 | GATTTAGTGGGTAGT[C/T]AATTTCAAGCCCCAT | 286053 |
rs560973559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169415 | CTTAAATGTGCTATA[A/G]GCTCCTTAAATTCAG | 286053 |
rs560974832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190995 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 286053 |
rs560982430 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096089 | ATGTAGGGCCTTGAG[C/T]TCCTTCCATGCAGTA | 286053 |
rs560983005 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196394 | GTGTGTGATGTTCCC[C/T]GCCCTGTGTCCAAGT | 286053 |
rs560983048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196218 | CTTTTTTTTTTTTTT[A/T]ATACTTTAAGTTCTA | 286053 |
rs560984496 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110895 | TGGGGGGAAGGAGCT[A/G]GGACCTTTCAGGGCC | 286053 |
rs561002995 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145766 | TTCTCCCTTCACCTT[A/G]AACATTTCTCTCCTG | 286053 |
rs561003941 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314159 | TTAATGCTTAAGTGG[A/T]TATCTAAGCAGCAGG | 286053 |
rs561009045 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220898 | TGTAATATATAGTTC[C/T]TTATTCTGTGGTTAA | 286053 |
rs561012830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321055 | CAGCACCAGGGGGAC[A/G]GTGCTAAACTGTTAG | 286053 |
rs561025687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148159 | TGTTCTTCAGCAGCT[C/T]GTCCCAACATTCTTG | 286053 |
rs561027539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095355 | AGCACTTGAGAGGCC[A/G]AGTTGGGAGGATCAC | 286053 |
rs561032017 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286452 | CAAGTAGCTGGGATT[A/C]CAGGCGCCCACCACC | 286053 |
rs561044943 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163999 | GTTGGAGGCCTTAGC[A/C]CAGGTCTGGATAAGA | 286053 |
rs561050488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281949 | ATGCTCTGTCTAGCT[C/T]GTAGCTTGCAAACTC | 286053 |
rs561059756 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267790 | CAAAAAATAGTAATC[A/G]GTACTTTATCTAATA | 286053 |
rs561080714 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305764 | AGTGTAATTTTTTCT[C/G]ACCAAAGTATAGCCT | 286053 |
rs561100515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155007 | CTCAAATAAATCTTT[G/T]AATAAATATTTACTG | 286053 |
rs561108189 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192638 | TTACACATTCAAATA[A/G/T]TACTAATGACTTGCT | 286053 |
rs561114767 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256078 | CACAAGGTCAAGAGA[A/T]CAAGACCATCCTGGC | 286053 |
rs561139909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139385 | TCTTTTTTTGTTTTT[A/G]ATATAGTATGTGTTG | 286053 |
rs561146036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247591 | TTAGCTGGGTATGGT[A/G]GCAGGCACCTGTAAT | 286053 |
rs561146540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153964 | CAAGAGTCATATAGG[A/G]TTAAGTATAGGCTAC | 286053 |
rs561155206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294741 | AATGACATGGAGTTA[A/C]GATTACACACTCATC | 286053 |
rs561163583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155570 | GTCATGGCAGTAGTT[G/T]ATTTAAGAATTATTT | 286053 |
rs561168746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286982 | CGATCTCACTGTAAC[A/G]TGCCTCCTCTGTAGG | 286053 |
rs561170942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279919 | CCCAGCGCAGTCATC[C/T]ATCCTCTCTATCAAT | 286053 |
rs561190596 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121813 | TCATTACCATTATAC[A/G]TATGAGTAAACTGAA | 286053 |
rs561199039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329967 | ATCACTTCTCTCCAG[C/G]CCCCTCCGAAAGAAC | 286053 |
rs561281396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330644 | TCCAGATTTCATTCC[A/G]TGCCTAATTACGTTT | 286053 |
rs561283717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163146 | CCGAGGTGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 286053 |
rs561298226 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170415 | TTTTTTTTTTTTTTT[A/T]AAGACAGAGTCTCGC | 286053 |
rs561322408 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111871 | ACCTGATATTTTCAG[G/T]GCTTGATTTTTTAGA | 286053 |
rs561326560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, splice-donor-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091001 | CCCTCACTACGCCTC[A/C]CCTATGTTTGAGGGA | 286053 |
rs561336915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134150 | AAAGCTGGTTTCTTT[C/T]ATATTTGTTATGTAA | 286053 |
rs561338190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300657 | TGAAGTTTACAGTCT[A/G]TGGGCAGTGGAGTAG | 286053 |
rs561342449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242447 | AGTTGTATCACCTCT[A/G]AAGTGTCCAAATGAA | 286053 |
rs561342971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206075 | TATCTATAAAATGAC[A/G]TGTTCAGAAAATGTT | 286053 |
rs561352285 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235434 | TATTTGAAAGTGAAA[A/C]GATAACTCCTCTGAC | 286053 |
rs561370366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308997 | CGCCTGTAATCCCAG[C/G]ACTTTGGGAGGCCGA | 286053 |
rs561376175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346396 | CTGTCTTGAGTACCT[G/T]CACAGGTGGTACTTA | 286053 |
rs561381820 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302715 | GAGGGGTTGGGGAGC[A/G]TGCAGGGGCAGTATT | 286053 |
rs561383854 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125099511 | ACAACATATGGAGCT[C/G]AAGGAGATGGAGAGG | 286053 |
rs561391925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198364 | TGAGATATGTTGCAT[C/T]GATACCTAGTTTATT | 286053 |
rs561415675 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278393 | GAATGTAGGAAGTTG[G/T]GGGTGGCACAGAAGC | 286053 |
rs561419926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170306 | TTAGACCAAAATCCA[A/G]AGTTGTCCTTTGTTC | 286053 |
rs561443182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104178 | TAATTTTAGTAGAGA[C/T]GGAGTTTCTTCATGT | 286053 |
rs561454867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191877 | CAGACTGAACACCAT[A/G]TAATAAGAATCTTGG | 286053 |
rs561461093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204005 | CTAGAATGTCATTGC[A/G]GTGAGACAGATGCTT | 286053 |
rs561476116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205495 | GCTGCTTTTGGTGAT[A/G]GTGCATCCCAGGAGA | 286053 |
rs561502034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106422 | TGGTGGCTCATGTCT[A/G]TAATCCCAGCACTTT | 286053 |
rs561517478 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192847 | GCTGCCTGCCAGATG[A/G]TGATAGATGATGATG | 286053 |
rs561518129 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337755 | CAAAAATTAGCCGGG[C/G/T]GTGGTGGCACATGGC | 286053 |
rs561542920 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189824 | TTTACAATGATATGT[C/T]GGCACAAACATATAG | 286053 |
rs561558382 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280777 | ATAGGAGTCAATAAC[A/G]ATTCACTGACTAATG | 286053 |
rs561559035 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272099 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 286053 |
rs561596202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212578 | GTTCAGTACCAAACC[A/G]TTGGAAGTCATTGCC | 286053 |
rs561617265 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308988 | GGTGGCTTACGCCTG[C/T]AATCCCAGCACTTTG | 286053 |
rs561620706 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298639 | TGGAATACCATTGAA[C/T]GTGACCAGTGGTTCT | 286053 |
rs561642804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354540 | TTTTAAGGTCTCAGA[C/T]GTTTGTTTAGCTCTC | 286053 |
rs561646347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309655 | GCTTGAGCTGGGGAG[A/G]TCAAGGCTACAGTGA | 286053 |
rs561649489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191020 | GGATTACAGGCACCC[A/G]CCACGCCACCTAGCT | 286053 |
rs561663733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345445 | TACATGACAGTATTC[A/G]AAGCATTCTCTTACT | 286053 |
rs561682955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158166 | AGCACTTTGTGGCAG[A/G]GTTTCTTGTGGCATC | 286053 |
rs561692928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316615 | CCTTCTTTCCTTTCT[C/T]TATTTCCTTCTTTCC | 286053 |
rs561693549 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275508 | CTGAGTTCTCTTCCT[C/T]TTACTGCCCTCTAAC | 286053 |
rs561705809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347226 | AATTTGCCCAAGAGC[A/T]CCCTGCTGATAATGA | 286053 |
rs561721834 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367370 | AAATCCAGAAATTAT[C/T]CAGGTGTGGTGGTGC | 286053 |
rs561735035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122357 | CATAACCAAAGCATC[G/T]GGCATTTGCTTCCCG | 286053 |
rs561736802 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099285 | TTGGGAGGGCTTGCC[A/G/T]TTGTATATCAGATGG | 286053 |
rs561737064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362145 | TGCACAGCGATGATG[C/T]GGCAGCTGAAGATCG | 286053 |
rs561744072 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103069 | TCAGGAGTTTGAGAC[C/T]AGCCTGGCCAATATG | 286053 |
rs561757953 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269951 | GTATGTACTTTATGC[A/G]AGGCTGAACTAAAGG | 286053 |
rs561766727 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353246 | GCATCAGTTCAGAAT[-/A]AATGGTGTACAAAAT | 286053 |
rs561768888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171817 | GTATTCTCTAAGTCA[A/G]CACTTCCCAGTGCCT | 286053 |
rs561773320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112653 | CACAGAAAGATAAAT[A/C]GTGCTTGATCTCACT | 286053 |
rs561786370 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243704 | TCCAGATGTGTGAGA[C/G]TCAGGTAAGGTGGAG | 286053 |
rs561792302 | in-del | -/TATACT | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149298 | AGATAGTCTATGAAA[-/TATACT]TATAAGTAACTATTA | 286053 |
rs561801445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134512 | ATTTGATTTTTCTAA[C/T]GATCATTAAAATTGA | 286053 |
rs561804834 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258629 | ATAATGGCATGAGGG[G/T]TCTAGAAAGTAAAAT | 286053 |
rs561809158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357607 | GTAATTATGTAAAGC[C/G]ATGAGAATGGGAAGT | 286053 |
rs561811055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355928 | CTGTTCAAAGCCAGT[C/G]CTGTCACTATCACTC | 286053 |
rs561822890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227884 | TCATTTTTTTAGTCA[A/G]TATAGTGTGAGCTCA | 286053 |
rs561828306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219483 | GCTGCTGCTGCTATA[A/C]TGCCTAGAGCTTGAC | 286053 |
rs561848135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241320 | AAGACATTGGCTCAC[C/T]CATGAAAATGTATAA | 286053 |
rs561853296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359720 | GAAATTTAAATAAGA[C/T]ACATGCAAAGTACTT | 286053 |
rs561853514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250864 | AATCCTGATCTTTAC[A/G]CAGGAAGATTTATGT | 286053 |
rs561856214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270321 | AATACAAAACTTAGC[A/G]GGGCATGGTGGCAGG | 286053 |
rs561872877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121748 | TTATAAATGCCTTAT[A/G]TGTATTCATTCATTT | 286053 |
rs561872968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125129880 | CCATACCCTCACACA[G/T]TTCCCTCAGTTGTTA | 286053 |
rs561883761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227456 | CTGCCTTACCGAATA[A/G]CGAATCAAATGTTTC | 286053 |
rs561893049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171180 | TTTCCACTCTGCTCA[A/G]TTGTTCTCCATGGCA | 286053 |
rs561905058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269649 | CCTTGTTTTATGCTT[C/T]GAGTATTTGCCTCTT | 286053 |
rs561914992 | in-del | -/GAAAGA | 0.0755793 | 0.179102 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284256 | AAAAAAAATACCCCT[-/GAAAGA]CAGAGTATGTCTTCG | 286053 |
rs561919797 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181149 | GGCAGCAGCTTGACT[A/G]TAGTGGCTAAAGCTG | 286053 |
rs561933969 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093126 | GGTAGCTTATGAACA[A/G]CAGAAATTTATTTCT | 286053 |
rs561943258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316063 | CCTCCCATCTCAGCC[C/T]CCCAAAGTGGTGGGA | 286053 |
rs561960839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275706 | GAGTCACCTAATGTG[C/T]TTTCGATGCCGTATG | 286053 |
rs561963938 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360307 | AACTATCGATGTGGA[A/T]TGGGAGGTTATCAGT | 286053 |
rs561967867 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249371 | TCCCCACATCACAGC[C/T]GACAGTCCATTTGGA | 286053 |
rs562037557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173134 | CCAATTCTGTCACCT[C/G]CCTTTTTGTCCCTGT | 286053 |
rs562045623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099946 | GGGAAAATTTAATGA[C/T]GCAGGAAAGCAGGGA | 286053 |
rs562045916 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092458 | AATATGTCAGGGTTC[G/T]AGTTTAAGGAGGTGT | 286053 |
rs562060272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264677 | TTCTTGAAGCTACTT[C/T]AGAACCGTGTAAGAG | 286053 |
rs562071934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333605 | CTGCAAGCTCCGCCT[C/T]CCGGGTTCACGCCAT | 286053 |
rs562083903 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348123 | GCTCCCTGAAGGCAA[G/T]GATTATTTTTCACCA | 286053 |
rs562088452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237304 | TTACTATAACCTAAT[C/T]GAGGGCATTGACATC | 286053 |
rs562107541 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277611 | TCCCAGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 286053 |
rs562111718 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147028 | TATACATATATAATC[A/G]TTGTCATTACTTTCC | 286053 |
rs562125166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278471 | CAGGTGCTGCCAGCA[A/G]AGCAGAGCGTGTGCT | 286053 |
rs562126687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187485 | TTTCTCTTCTCCTTG[C/G]CTTAAACTGCCTTCA | 286053 |
rs562149238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244501 | CCATGCAGTGACTAC[C/T]CTATGTTGTTAAAAG | 286053 |
rs562154755 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281465 | TTTTTTTCTAGAGAG[A/G]GTCTTGCTCTGTTGC | 286053 |
rs562157622 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271059 | GAGGTCAGGAGTTCA[A/G]GACCAGCCTGAACAA | 286053 |
rs562171798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265471 | GGTGATCCACCCATG[G/T]CGGCCTCCAAAAGTG | 286053 |
rs562173192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180254 | TGAGCTTTATTCGTT[A/C]TTTAGCCATACAGTA | 286053 |
rs562175182 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115673 | GGAGAATTGCTAGAA[C/T]CAGGTGGGTGGAGGT | 286053 |
rs562175255 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172668 | TTATTTTTATAAAAC[A/T]TTAGGAGAAAAAGAG | 286053 |
rs562179970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136898 | AAAAAATAAAAATTA[C/T]CTTCTAAAATGTGAG | 286053 |
rs562180114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348764 | ATTGTAAGGCCTCTC[C/T]AGCCACGTGGAACTG | 286053 |
rs562186896 | in-del | -/A | 0.0364509 | 0.129988 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161302 | TGGACTTCCTTTTTT[-/A]AAAAAAAAAGTCTAA | 286053 |
rs562191658 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299966 | TGGGACTACAGGTGC[A/G]CGCCATCATGCTTGG | 286053 |
rs562210963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311690 | TATTTTGGAAGAAAT[C/T]TGAAGAATGTAATGT | 286053 |
rs562278226 | in-del | -/AGCG | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259349 | GGTGAGCAGCCCACA[-/AGCG]AGCATTACCACCTGA | 286053 |
rs562281971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145514 | CATGTATTTATTGGC[G/T]TGTAAATGAATGTTC | 286053 |
rs562305958 | in-del | -/TTTCTTTTTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267000 | AACTTTTCTTTTTTC[-/TTTCTTTTTT]TTTTTTTTTTTTTGA | 286053 |
rs562317088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179691 | GGGGGGAAAGCACAG[G/T]GAATCACTAAAAATT | 286053 |
rs562337177 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259029 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 286053 |
rs562337277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252181 | GTAAAGAGAAGCTAA[C/T]GTATGAGACTGGAAA | 286053 |
rs562347833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150662 | ACTAGGATTACAGAC[A/G]TTAGTCACCACGCCC | 286053 |
rs562355046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238959 | TTGATGTTTAATGAT[A/G]TGGGGCCGAATTGTT | 286053 |
rs562357672 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152163 | AACTATAGTATTTGA[A/C]TAACTTTAAGAATAT | 286053 |
rs562362885 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315308 | CTTTACCTCAAAGCC[A/C]CAGCTTCCACATCAG | 286053 |
rs562368778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106829 | GACGAAAACCTGTCT[C/G]TACTAAAAATACAAA | 286053 |
rs562373975 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283908 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG | 286053 |
rs562376977 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203193 | GTTTAGTTAGCCTTT[-/A]AAAAAAAAAAAAATC | 286053 |
rs562387024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142665 | GCTGGAGGACAGTGG[C/T]GCTATCTTGGCTCAC | 286053 |
rs562426727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319571 | TTACATATGTAAAGA[C/T]CCAATAAGATGAAAC | 286053 |
rs562428087 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178119 | CTCTCAGTTGTGTGT[C/T]CTCCAGGCATTAACA | 286053 |
rs562429134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095148 | GAGCCACCTTTCCAG[C/T]CAGGTTTTAGATAAT | 286053 |
rs562459078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188736 | GAATGGTTTTGCTTT[C/G]AGGATACTGCGAACT | 286053 |
rs562474747 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252480 | GCAGTGAGCTGAGAT[A/C/T]CCGCCACTGCACTCC | 286053 |
rs562482119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138042 | TAGCTGATGAATTAG[A/G]TAAGATTGAAATTCA | 286053 |
rs562483110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189161 | GTCAGCACAGAGACA[A/G]AGGACCTCTCAGCAA | 286053 |
rs562483809 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327181 | TGAGGCAGGAGAATC[A/G/T]CTTGAACCTGGGAGG | 286053 |
rs562483967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334909 | ACAGGATGTACACCA[C/G]CACACCCGGCTAATC | 286053 |
rs562487362 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285916 | GTCTCAGTGACTGTG[C/T]CAGGATTTGAATTCA | 286053 |
rs562523458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195520 | ATTGTACTTGGTGTC[C/G]TGGTTTTAAATATAA | 286053 |
rs562533736 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159348 | CATATGATGGTGGTG[A/C]CATAAGATTATAATA | 286053 |
rs562535641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196986 | ATGCGTCTGTTGGCC[A/G]CATAAATGTCTTCTT | 286053 |
rs562545180 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341843 | CAACTTGAAGCCACC[A/G]AGGACCCTTTAGGAT | 286053 |
rs562558081 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164321 | GAGACTTGAACCTCA[G/T]TGTTTTGACATGTAA | 286053 |
rs562558759 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193214 | CATTTATGTAAAGTA[C/G]ACTTCATCAAAATTA | 286053 |
rs562567445 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293291 | AGTTTATCAAGGGAG[A/G]TACAAACTTGGCAGT | 286053 |
rs562576929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096189 | AAATGTGGCTTTTTG[C/T]AGATTAGGCCTGGAA | 286053 |
rs562580564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299867 | TCTGTCACTCAGGCT[A/G]GAGTGCAGTGGCAGA | 286053 |
rs562593622 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115365 | TAACAAAGCCTATAT[A/G]TTGGAGGAGCTTCAG | 286053 |
rs562600084 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328148 | CAAAGACTTCTCACT[A/G]GCCTTTTTTTTTTTT | 286053 |
rs562602165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214454 | AGTCATGGGGGCTCA[C/T]GGTCTCAACAAGGAA | 286053 |
rs562629782 | in-del | -/AA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108042 | CTGTCTCAAAAAAAA[-/AA]TAAAAAAAATTATGA | 286053 |
rs562651575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239581 | GCCACTGCACTCTAG[C/T]CTGGGCGACAGAGCA | 286053 |
rs562654348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107975 | GGTGGCAGAGGTTGC[A/G]ATGAGCTGAGATCAC | 286053 |
rs562655375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159746 | TGGTGGATCACTTGC[A/G]GTCAGGAGTTCGAGA | 286053 |
rs562663299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201644 | AGTTAGGCTACACAG[C/T]GCTCAGGGACCCACT | 286053 |
rs562672521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202447 | CTAAACCATGGAAAG[A/G]TAACTGGAATCTGAA | 286053 |
rs562673473 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169622 | ACCTACCTCCATTCC[C/G]ATGTTCACAGTCTTC | 286053 |
rs562704858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305532 | CTGGAAAATCAGACC[C/T]GTAGCTCAGGGGTGC | 286053 |
rs562705903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297523 | TTCCTTCTGGAATGA[A/G]ACACAGTAAAAACTA | 286053 |
rs562707867 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304761 | GCTTGGGAGACTGAG[A/G]CATCAAGTCTCATCA | 286053 |
rs562709848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101900 | TGTTGGATAGTTTAA[C/T]GATTACAGGTTTTCA | 286053 |
rs562717145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175454 | AACTGCTTATCACTA[G/T]TATGTGTCTGTGATA | 286053 |
rs562748390 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341922 | AAAAAAAAAAAAAAA[A/C]CCTGTCTCTGCCCAT | 286053 |
rs562769077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215131 | GTGCCATGCTGGTGC[A/G]CTGCACCCACTAACT | 286053 |
rs562779553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168623 | AACAAGCTCTCTGGG[A/G]CCTCTTTTATGATGG | 286053 |
rs562794079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110379 | GGGCAGAAAGATTAC[A/G]GTTACTATGGTCAGG | 286053 |
rs562799101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201041 | TTTAAGGTCTTCTCT[A/G]TACTGTTTATTCTAG | 286053 |
rs562799611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167164 | CTAGTGCAAGATGGC[G/T]CTTTACCACCAGATA | 286053 |
rs562802186 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199679 | TGGAGAGTTTTGTAG[A/G]TGTCTATTAGGTCTG | 286053 |
rs562814475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240749 | TAATGCACTTAGCAT[A/T]TTCCTGTCTAATCAA | 286053 |
rs562815368 | in-del | -/TATTA | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089933 | TATATATAAACTTTA[-/TATTA]AATTTTTAATGCAAA | 286053 |
rs562831035 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120336 | ACTCAAATCAAACCA[A/G]TCGGTAAAACGAGTT | 286053 |
rs562832215 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207795 | CTTCAGCTGTGACAG[C/T]TGATCCCTGCTCCAT | 286053 |
rs562833419 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367464 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC | 286053 |
rs562835983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259651 | GGAACAGCAACATCT[C/T]ACCCTGTGGCCTACT | 286053 |
rs562841309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306494 | CCACACAGTGAAGAG[A/G]TATGATGCAGCTCCA | 286053 |
rs562849044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286538 | GGCTGGTCTCAAACT[C/T]CTGACCTCAAGTGAT | 286053 |
rs562849639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351733 | ATTGTGGGGTTGGCC[A/G]GGCATGGTGGCTCAC | 286053 |
rs562850832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154002 | ATTGCACAAGGTGTT[C/G]ATGGCCTCTGAAATG | 286053 |
rs562869261 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139538 | CAGAAGGCAAAGGAG[A/T]AGCAGAGTCATGTCT | 286053 |
rs562885186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336140 | TGAAGATAGGAAGGA[C/G]AGAGCATTGAGGCAG | 286053 |
rs562895919 | snp | C/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283949 | ACAAGGTCAGGAGAT[C/G/T]GAGACCATCCTGGCT | 286053 |
rs562899507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103500 | GAGATTTATGGATCT[A/G]TCAGCTTATAGTTTT | 286053 |
rs562922599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117396 | CCAGCCTTCAGTCTC[G/T]TTGGCTTTTTGTGTG | 286053 |
rs562923434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266603 | TATAGTTGGAGAGAA[C/T]AGAATGCTGTCTCCA | 286053 |
rs562932434 | in-del | -/T | 0.346033 | 0.230819 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254606 | CTGTTTACCTCAGAT[-/T]TTTTTTTTTTTAATA | 286053 |
rs562941680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358666 | GGATTTGTTGCAGGA[A/G]TGGAATTGCAGGTGT | 286053 |
rs562944267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208848 | AATTAGAGTCTTTTC[A/G]AGTGGCAAGTATTAA | 286053 |
rs562959534 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282300 | TGTATTTTTAGTAGA[C/G]CCGGGGTTTCACCAT | 286053 |
rs562966297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226611 | TGGGGTTCTCACTTT[C/G]TGACTCCTGGAGGAC | 286053 |
rs562966369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160812 | AAAATGTATTTCTCT[C/G]TGTGTACGAGTACAC | 286053 |
rs562966783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125363876 | CTGATCCTCTTTCAT[A/G]TAATTGCCTTTCTGT | 286053 |
rs562967233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209523 | TAATTGAATAGTACC[A/G]TATTTAAACTTATAC | 286053 |
rs562968152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217409 | TGTGTCACCCAGGCT[A/G]AAGTGCAGTGGCATG | 286053 |
rs562987750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161589 | GATCATCTGAGGCCA[A/G]GAGTTCGAGACCAGC | 286053 |
rs562987797 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312865 | AGTCATTAGAAAAAG[C/T]CTCTCTGAGGAAGTG | 286053 |
rs563007436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293580 | GGAACACAAACAGGA[A/G]GAAGGTTTAGTCATC | 286053 |
rs563015506 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110992 | CTAAGCAACAGCTCT[C/G]ATGTTTGCTCTTCTT | 286053 |
rs563029333 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095341 | ATGCCTATAATCCCA[-/G]CACTTGAGAGGCCGA | 286053 |
rs563048618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133372 | AAAGACTGAAATAAT[C/T]CAGGGGTGTAAAATG | 286053 |
rs563052888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352401 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 286053 |
rs563059934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313180 | AAGGAAGGAAAGAAG[A/G]AAGGAGAAAGAAAGA | 286053 |
rs563060430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260256 | CTGGAAGAATCTAGT[C/T]CCTTAGGCTAAGTCA | 286053 |
rs563060834 | in-del | -/T | 0.188104 | 0.242216 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265160 | CCTGGCTTTATTTAA[-/T]TTTTTTTTGGTAGTT | 286053 |
rs563063620 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356616 | AAAGGCGTGAGCCAC[C/T]GCAACCGGCCTTATT | 286053 |
rs563074851 | in-del | -/TT | 0.0103295 | 0.0711199 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188219 | ACCTTCGCTTTACTA[-/TT]TTTAGTTGGTGGCTT | 286053 |
rs563098763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223474 | CTCTTTGACATACCA[A/G]TTTCATTTCATTTGT | 286053 |
rs563101790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216475 | AGAAACCCGCTTTCT[A/C]CTAAAAATACAAACT | 286053 |
rs563136797 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100761 | AGACAGGGTTTTGCC[A/G]TGTTGGCCATGCTGG | 286053 |
rs563143830 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248585 | CTGAACCAGGGAGGC[A/G]GAGGTTGCAGTGAGC | 286053 |
rs563155018 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260646 | ATTTTCTTTTTTGAG[A/G/T]TGGAGTCTTGCTCTG | 286053 |
rs563174328 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223484 | TACCAATTTCATTTC[A/G]TTTGTATGTATACCC | 286053 |
rs563175274 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261901 | CAGGAGTTCAAGACC[A/G]TCCTCGCCAACACAG | 286053 |
rs563177375 | snp | A/G | 8.24559e-05 | 0.00642037 | missense | NSMCE2 | GRCh38.p7 | 8:125357311 | AACTTCACCTGCCCC[A/G]TTACAAAGGTACCGC | 286053 |
rs563198936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197717 | AAGTAGTTTTTTCCA[A/G]TTCTTTGAAGAAAGT | 286053 |
rs563201135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123935 | CCATTTAAAATGTAC[A/C]ATTTTGTGGTTTTCA | 286053 |
rs563205552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262927 | ATTTCAGTGCCTCCG[C/T]GAAAAAAGGTTGAAG | 286053 |
rs563211863 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180895 | CTACCTACTGTGTGC[C/T]GGGCACTGGTAATAC | 286053 |
rs563214685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267087 | TTGGCCTACTGCAAC[C/G]TGTACCTCCTGGGTT | 286053 |
rs563231108 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260477 | CCCCACTAGATCTGG[G/T]TTCTAGCCCTCCCTG | 286053 |
rs563232247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308925 | GCTTGATAACGTGGG[C/G]CCAGCGTGCAGCTGT | 286053 |
rs563239797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170444 | GCTCTCTTGGCCTCT[C/T]GGGCAGGCTGGAGTG | 286053 |
rs563248658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359487 | TACAGGCATGCACCA[C/T]CACGCCCAGCTAATT | 286053 |
rs563254050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307901 | CCACATAGTTGTATA[C/T]GCATATGTCAGTTTG | 286053 |
rs563265165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096713 | CCTCCAGGATTCAAG[C/T]GATTCTTCTGCCTCA | 286053 |
rs563269072 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226257 | CATTGTGTAGATTTG[C/T]TTTTAAACATGTCCA | 286053 |
rs563270132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126247 | AAATTAAGCTGGCAT[C/G]GTGGTGGGTGCCTAC | 286053 |
rs563273535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330386 | TCACCACGTTGGCCA[A/G]GCTGGTCTCGAACTC | 286053 |
rs563281614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125195994 | TGGGTTCAAGCAATT[C/T]TGCTGCCTCCCAAGT | 286053 |
rs563288002 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268571 | TTAGGTTGTTGGGGA[G/T]GCAGACCTGGAATCA | 286053 |
rs563289224 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309875 | CTAGAGCATGATCTA[A/T]TAAGATTGGACTGTC | 286053 |
rs563289455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322146 | CTAAAGTGGGAGAGT[C/T]GCTTGAGCCCAGGAG | 286053 |
rs563330929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365909 | GCCCCATTGGCGCAC[G/T]GACCTCACTTCCAAC | 286053 |
rs563355227 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336497 | GGAAGGAGGATTGGT[A/T]ATATGCAGAGTCAGA | 286053 |
rs563363838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125411 | CTATTATCACAGAGC[A/G]GGTATTGAAGGGTGA | 286053 |
rs563374142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169527 | TCCTATCAGAAATCT[C/G]TTGTCGTCCTTACTT | 286053 |
rs563376746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184755 | GATTTTCTTTCTTTA[C/G]ATTTAACACTGTTGT | 286053 |
rs563386802 | snp | A/C | | | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125129966 | CATTCCTGTTGACTA[A/C]ACTAAATAGTAAGCT | 286053 |
rs563387215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190104 | GGCTGGATTGCATCC[G/T]GAGAGCTTATGTTCA | 286053 |
rs563395932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270358 | TAAACCCAGCTACTC[C/G]GGAGGCTAAGACATG | 286053 |
rs563423222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234303 | AGAAGAAATGAACAA[A/G]TACATTTTGGCCATA | 286053 |
rs563458443 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193536 | TCTTTATCTACCTTC[A/G]TTTTTTAAAATGTAT | 286053 |
rs563463093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276258 | GGAAGCCCTTAGCCA[A/G]TCAAACAGAATGGAA | 286053 |
rs563475921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184027 | TCAATCTTGAAAAAA[A/C]AAAGATGCTAATGAA | 286053 |
rs563480999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142498 | CTTGAGGATTTCTCC[C/T]ATATTCACTGTGTTT | 286053 |
rs563502420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148286 | CCATTTCCTCCTTTG[C/T]AGGAAGGTCTCTTTG | 286053 |
rs563502664 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250475 | CATAGCATTAAACAA[C/T]TACTGTTTCCTTACT | 286053 |
rs563504722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277955 | TTTGGGCAGAAAGTT[A/G]TTTTTAATTGGGTAT | 286053 |
rs563520051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346456 | GATGAGTGCAAAGGG[C/T]GCTCCTTACCTTCTG | 286053 |
rs563529615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187400 | GAAACAATATGATTC[A/G]GTTTAAGGCAGACAT | 286053 |
rs563532311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274803 | GGCATGGTGGCGCAC[A/G]CCTGTAATCCCAGCT | 286053 |
rs563543283 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243810 | AATAATGGAGCATCC[A/G]TCACCTTAGGCATTA | 286053 |
rs563544035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249139 | TCATGCCACTGTACT[C/G]CAGCCTGGGTGACGG | 286053 |
rs563544159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256743 | ATCCTGGCTAACATG[A/G]TGAAACCCTGTCTCT | 286053 |
rs563552710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147177 | CCCACCACTCCAGTG[C/T]TGGTGCCATCTCTTT | 286053 |
rs563557894 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346799 | GGGTTTTGATTATTT[C/T]AAACCTAATATTTGG | 286053 |
rs563570241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178867 | GAGACTCCGCCTCAA[A/G]AAAAAATGATAATAA | 286053 |
rs563572006 | snp | G/T | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090101 | AAGAAGTTAAAACAA[G/T]ATTAGCTGAAAGAAG | 286053 |
rs563578105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289066 | AGTGCTGGGATTTAC[A/G]GGCATGTGCCACCAC | 286053 |
rs563590910 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150729 | GTCCAAATAATCTAG[C/T]TCTGTGTTATTAAAA | 286053 |
rs563591233 | in-del | -/CTC | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190174 | TGAGTATTTGCCTCT[-/CTC]CTCTTTCCTCCTCTC | 286053 |
rs563593077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112108 | CAATAACCCTAAGAA[A/G]CCAATGTTTGTATGC | 286053 |
rs563595494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273768 | TATGGCCCTGTTCCT[C/G]ACTCATATTGCAGAT | 286053 |
rs563616684 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191024 | TACAGGCACCCGCCA[C/T]GCCACCTAGCTAATT | 286053 |
rs563634014 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092041 | ACGGGGACTCCGAGC[C/T]GGGGGTCCGTCTACC | 286053 |
rs563654385 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154716 | TGATATTTTCAGTCA[A/T]AAGACCAACATGTCA | 286053 |
rs563654651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112409 | GGTATGTATCCAAAG[A/G]ATGTATGTCAAAGAG | 286053 |
rs563677192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178350 | TGGATGAGTAAGCGG[A/G]TGGTACAGAAAAATC | 286053 |
rs563678631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323948 | AAAGATCTCTCAAAA[C/T]TCAATAAGAAGAAAG | 286053 |
rs563688738 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355607 | CAGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC | 286053 |
rs563712099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235490 | GTCATTTTTCTGTGC[A/G]TAAGCAAGAATATGC | 286053 |
rs563718395 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327791 | TATGTATACAATTGT[C/T]TTAGGATTTAAAGGC | 286053 |
rs563727141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105329 | CATAATTTAGCTTTG[A/G]TAGATAGGCCTGGAT | 286053 |
rs563727957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194238 | AAATTCTCCTGTGCC[A/G]CTTTGTAGTTGACTC | 286053 |
rs563760021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228180 | AGATTAAATAAAATT[A/G]TGGTATATTTTTCAG | 286053 |
rs563775064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296645 | AAGTGATCCACCCAC[C/T]TTGGCCTCCCAAAGT | 286053 |
rs563784404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339064 | ATGTTGGTAATTCAC[A/C]TGGGGAGAGGATACA | 286053 |
rs563791282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193439 | AGATAAACAAATGGC[C/T]AATAAACATATGAAA | 286053 |
rs563795659 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091731 | ATCCGCAGTCCCGGA[C/T]CTGGAGCGGGTCAGA | 286053 |
rs563804145 | snp | A/G | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092930 | TCCTGTGTTTTGTAG[A/G]ATGCTTAAGAGCATC | 286053 |
rs563816351 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164145 | GAAATTCTGAAACCA[A/G]CATTCTTTCCCTCAG | 286053 |
rs563822365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227514 | GGACAACTTTTATTA[A/G]CATCTTTGTCTAAGC | 286053 |
rs563829250 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367392 | TGGTGGTGCGCACCT[A/G]TAATCCTAGCTACTC | 286053 |
rs563845149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134750 | TTTTTTTTTAAGAGT[C/T]GGGGTCTTGCTCTGT | 286053 |
rs563849461 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276393 | CTAAAACCCCTCTTC[C/T]TTACTCCAGACTAAC | 286053 |
rs563865802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198931 | GAGGGCATATGTGTC[C/T]AGGAATTTATCCATT | 286053 |
rs563896994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302903 | TGCCTCCAAACAACT[C/G]TGGGAATCCGGGACA | 286053 |
rs563902308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097988 | GTCTTATTAGCAAGC[C/T]CAAAGACCTTAAGGT | 286053 |
rs563903340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164882 | TGAGCCAGGCAGTAT[G/T]CAGTTATCTCCGGTT | 286053 |
rs563904636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302021 | CTGGAGTGCAGTGGC[A/C]CAATCTCAGCTCACT | 286053 |
rs563927427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331542 | AAACTTAGCATGGGA[A/T]AGATGAAAACTATAG | 286053 |
rs563967898 | in-del | -/T | 0.472241 | 0.114494 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272014 | TCTGCAGTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs563983127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333670 | CAGGCGCCCGCCACT[A/G]CGCCCGGCTATTTTT | 286053 |
rs564008186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155742 | AAACTGTGGGCTTCA[A/G]ATTGCTCAGGGTAGG | 286053 |
rs564031552 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269385 | GCCACTGCACCCAGC[C/T]GACTCTTTAACTGAG | 286053 |
rs564052864 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338563 | TTCGTTAGCAGTAGC[A/T]ACAAACATTTCATCA | 286053 |
rs564100144 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216860 | AGTGAAATCAGTGAT[C/T]AAGGGAAAGTAAGAT | 286053 |
rs564126327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361109 | TTTTCCTTTTTTTTT[C/T]GAGACAGAGTCTCAC | 286053 |
rs564128584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213196 | AGCTTTTATTCTCTG[A/T]TGTGAGATTTTCCCC | 286053 |
rs564133068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115854 | GGTGAAGAAAAGGGA[G/T]CTGTCATAGCCTACA | 286053 |
rs564149517 | in-del | -/T/TT | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281446 | GTATCGAGAGGGTGA[-/T/TT]TTTTTTTTTTCTAGA | 286053 |
rs564163431 | in-del | -/TG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246120 | TAATATTTTTAACTC[-/TG]TGACAATTCAGTTTT | 286053 |
rs564163896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222592 | TTAGCCTGTTTTAGA[G/T]TCCACGTGTAAGTGA | 286053 |
rs564217711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283554 | AGATCTTGGTTTGGG[C/T]ACCCATTTTGCCTCT | 286053 |
rs564235324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220867 | TTTGGAATTTGAGTT[A/G]CTGCCAAGTCTTGTG | 286053 |
rs564250966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333049 | ATTGATTGTTGCCAG[C/T]GAGCTTCGTTCCAAA | 286053 |
rs564266248 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113717 | ATTTCCCCCGTCATC[A/C]TCTCCTTTCTCATCA | 286053 |
rs564272878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115472 | TTAAATCTTTCAGGC[C/T]GGGCTCAGTGGCTCA | 286053 |
rs564278717 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215262 | TGTTCTCATTGTTCA[A/G]TTCCCACCTATGAGT | 286053 |
rs564281947 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304820 | TTGAACCCTGGAGGC[A/G]GAGGTTACAGTGAGC | 286053 |
rs564292662 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316926 | TGGCACTATAGGCGT[A/G]TGCCACCACACCCAG | 286053 |
rs564297593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263719 | CATGGCACTGCACAC[C/T]AGCCTCCGTGACAGA | 286053 |
rs564325054 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300415 | TGATCCTCTTGCTTC[A/G]GCCTCCCAAAGTGCA | 286053 |
rs564326563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309781 | GTTTCACATGAGGCC[A/G]TGGACTTCTCAATCA | 286053 |
rs564327400 | in-del | -/AAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345042 | CTTAAAAAAAAAAAA[-/AAA]CCTCCACATTTTTGA | 286053 |
rs564343348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311850 | TTGGGAGGCCAAGGC[A/G]GGTAGATTACCTGAG | 286053 |
rs564343897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347883 | GAACATTGATCAGAA[C/T]GTTGACCTGAGGTGG | 286053 |
rs564371033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239445 | AAAGCCCCATCTCTA[C/T]TAAAACTACAAAAAT | 286053 |
rs564401573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120999 | AAATGCTACACAGTG[A/T]TTTTCATCACTATTT | 286053 |
rs564421559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318689 | AAAAAAAGAAAACAA[A/C]ATCTGTGAAACAACC | 286053 |
rs564427562 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221661 | ATACATAATGAAATA[C/T]ATTAGGGATAAGACC | 286053 |
rs564436159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257565 | CTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 286053 |
rs564438803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167242 | TTATCTAAATATGTA[C/G]AAGAAAGTTGAGATT | 286053 |
rs564453510 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259135 | TTGAACTCCCGACTC[A/T]GGTGATCCGCCCACT | 286053 |
rs564460373 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093691 | TCATGCCACTGCACT[C/G]CAGTTTGGGCGACAG | 286053 |
rs564463364 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209303 | AGACAAAAGTAAGGA[A/G]ACCCCCATTGAGTGA | 286053 |
rs564465298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265559 | AATTATTGCGTTAAA[A/G]TGCTGCTATCTTTAT | 286053 |
rs564483488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317847 | TCAAAGCAAAAATTA[C/T]CAGACCAGAATGCCA | 286053 |
rs564491328 | in-del | -/TAACATGAGCTGAG | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225138 | ATATGTGCTAATCCC[-/TAACATGAGCTGAG]TTTGAGAACTTAATG | 286053 |
rs564521605 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153512 | TTGAAGCTAAGGATA[C/G]TGCTATCTTATTGCT | 286053 |
rs564523295 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177874 | TTTAAATGTTTCTAG[C/T]TTCGTACTAGGTAAC | 286053 |
rs564524788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272741 | TATACACACACACAC[A/G]TATATATACACACGT | 286053 |
rs564547186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132005 | ATTCATGTCATGCAT[C/T]CTTAGAGTTTCTCAG | 286053 |
rs564553442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240439 | ACAGCTTTCAGAATT[A/G]CATTACTGTCTTCAG | 286053 |
rs564563849 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104836 | GAGGTCAGGAGTTCC[A/G]GGCCAACCTGACGAA | 286053 |
rs564568167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298321 | CAAGTACTTTGTTTA[A/C]GTTAACTCATTGATC | 286053 |
rs564570584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130548 | AGCTATTTTTCCAAG[A/G]GCCCTGGTTCTTTTT | 286053 |
rs564593159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330269 | GCAGCCTCCATCTCC[C/T]GGTTCGAGCGATTCT | 286053 |
rs564600853 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114681 | CTTCAGTGAATGGGA[C/T]AGCCCCTGCACAGCA | 286053 |
rs564602969 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135279 | TGGTCTCAAATTCCT[-/G]GCCTTAGGTGATCCT | 286053 |
rs564624626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138576 | TGTGTGATCAGGTAG[G/T]ACAAATGTAATAGTA | 286053 |
rs564633888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123258 | AGTTCTCCTAGACTC[A/G]GGTGTGTTTATAATA | 286053 |
rs564644131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188216 | AACACCTTCGCTTTA[C/G]TATTTTTAGTTGGTG | 286053 |
rs564678174 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223667 | TGCTAATAGCCATTC[C/T]AACAGATGTGAAGTG | 286053 |
rs564681186 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149106 | TGACCTGAGCCTTTT[C/T]TCACGCACCATTTTG | 286053 |
rs564686575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139170 | CAGATAGTTATATCA[C/G]GGCTTTTTAGGAAAT | 286053 |
rs564711633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173158 | TCCCTGTTCTGTGTC[A/G]TGAGGAGTTCAGAAT | 286053 |
rs564719031 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347750 | GAAAGGAGATTGGCT[A/G]TGGAGATTGTGTTGG | 286053 |
rs564723757 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272036 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 286053 |
rs564729427 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199520 | AATCCTGAGTTCTAA[-/T]TTGATTGCACTGTGG | 286053 |
rs564732874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124049 | AGCTATTGCCTTCCT[A/G]TTTTCCCATTCTCAC | 286053 |
rs564735923 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340023 | TTTTGTTTTTTTTTT[G/T]TTTTTTTTTGAGACG | 286053 |
rs564738231 | in-del | -/GAAGGG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320310 | AGGAAGGAAGGAAGG[-/GAAGGG]AAGGAAGGGAAGGAA | 286053 |
rs564754847 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144045 | GGACGTGATAGGGAA[A/C]AGAGGGGGGGAAAGT | 286053 |
rs564757142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187595 | TTCTTCAAGTCATCA[A/G]GCAATCTTTCTGGCG | 286053 |
rs564787754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231387 | GTAAAATAGCAGTTA[C/T]TGCAAGAACAAAGGG | 286053 |
rs564794355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108691 | GAACTTAGAAGAAGG[G/T]CCTGTGATGTGAAGA | 286053 |
rs564799126 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364432 | CTTTCTTTCCTTCTG[A/G]TTTGCATCTTTACTG | 286053 |
rs564812912 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239741 | GAGGCTGAACATAAC[A/C]TTTGTAAAAATATAC | 286053 |
rs564817375 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137086 | TCATGAAATCAAAAT[A/T]TTTTTTTTACTTTCC | 286053 |
rs564826333 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237117 | AAACAACACTTTGTG[A/G]AACTGTAGGCAAATG | 286053 |
rs564834434 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107139 | AAACCTGAATAACCA[C/T]AGTTTGTCTGTGAAT | 286053 |
rs564853652 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109960 | TTTTTTCAGGTTTTT[G/T]AGTTTATTATGTACT | 286053 |
rs564874211 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246892 | TTACCATTTTCTTTT[C/T]TTTCTTTTTCTCTTG | 286053 |
rs564875522 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131553 | AACTTATGCACACCT[C/T]GCCCAGCCAACAGGT | 286053 |
rs564878669 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182684 | TTTCTCTCAGAAGAC[C/G]ACTTTATCTTCTCAA | 286053 |
rs564878708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136772 | TTATGAATTATTACT[A/G]TTTTTCAATAGGAAG | 286053 |
rs564882828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279705 | ATAATCAAGTGTGTC[A/G]TCTTGATTATTAGGA | 286053 |
rs564907288 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216720 | GTTTCACTGTCTGAA[A/G]AATCTCCTGCTTCAA | 286053 |
rs564915219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328931 | AGAACTCCTGGCCCC[C/T]AGTTCAGCACCTTCT | 286053 |
rs564922111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191118 | CTCAGGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 286053 |
rs564926759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094657 | CATAACAAAATACCA[C/T]AGACTGGGTGGCTTA | 286053 |
rs564936399 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115665 | CTGAGGCAGGAGAAT[C/T]GCTAGAACCAGGTGG | 286053 |
rs564937525 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105136 | CCTTTGTCCTACTGT[C/T]CCACAGCTATTGTTT | 286053 |
rs564938928 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128352 | TGACTTGGACTAGAA[A/G]GGTGGTAAGGGATTG | 286053 |
rs564947435 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307467 | CCTGTTGAGCTGCCA[A/G]TTGGAAGACCCTAGT | 286053 |
rs564954570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313383 | GGGAGAAAAAGTTAA[C/T]AGTTGAGTTAATTTA | 286053 |
rs564984942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184131 | TGGCAGACTTAGCAT[C/T]CAATCACAATTCCTG | 286053 |
rs564990902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328335 | ATAACTGTAGTCTCC[A/G]TTTAAGAATCAATTT | 286053 |
rs565039980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101926 | TTTCAAAATAGTTTA[A/C]TAATAAACTATTTTA | 286053 |
rs565043226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285961 | AAAACTTGAGCCCTT[A/G]GCCATTAGGATGTAC | 286053 |
rs565049660 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134650 | GTTCTTTGTATACTC[A/G]GAATAAAAATTCTTT | 286053 |
rs565062449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196170 | ATCACAGGCATCAGC[C/T]ACCAAGTGCAGCCCT | 286053 |
rs565084856 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132921 | ACCCTTAGGCCTGAA[A/G]TGCACTTTACAGGTC | 286053 |
rs565103009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169365 | TCATCTTAGAACCAC[A/G]CACATAAACTTAATG | 286053 |
rs565109838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299013 | TGCATACCCAAGGTA[A/G]CACATTTCAGGAATA | 286053 |
rs565111158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291166 | AGCAGAAACTTTCAG[A/G]GGTAGGTGATGGTGT | 286053 |
rs565120373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095189 | GTGCCTAGTGCCTAT[C/T]ATATTGGACAGTGCA | 286053 |
rs565120816 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337048 | TGAAATTATGGGTTT[G/T]CATGAATTGCAACTA | 286053 |
rs565125022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198330 | GCTGTGGGTTTGTCA[C/T]AAATAGCTCTTATTA | 286053 |
rs565146472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141047 | ATTCCCATAGCCTGA[A/G]TTTCCATAGTGTTTT | 286053 |
rs565150065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208645 | ACAAATGATTGAGTG[C/T]CAGCGTAAGTGTTTC | 286053 |
rs565171494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162598 | TATCTGCCCCTCCTA[G/T]CTAGTGATTTCTTGA | 286053 |
rs565177021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160589 | TGGCCAGCTGCATTT[A/G]AACTTCCCTGATAGT | 286053 |
rs565180692 | snp | A/T | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093450 | TCCCAGCACTTTGGG[A/T]GGCCAAGGCGGGCGG | 286053 |
rs565202640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103571 | AATATATTTTTTTAA[C/T]TCCTCTGCTCTCCTC | 286053 |
rs565229734 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169048 | AGAGAATATTGTTCA[A/G]TTGTTCTCTTATTTG | 286053 |
rs565240644 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147386 | CTATAATTCTTTGTT[A/G]GATCCTAAGAACACT | 286053 |
rs565262321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345297 | TGAACAATGGTATGA[C/T]CTACACGGTATAATG | 286053 |
rs565272844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104685 | TCACTCTCTTGCAAA[A/C]CCTGCTGGCTGCCTC | 286053 |
rs565279130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248417 | GCAAAATTAATATCA[G/T]CAGGCTAAGGCAGGC | 286053 |
rs565283771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330099 | TAGCTTTACAGATTC[A/G]GGGCACGTCGCTTTC | 286053 |
rs565290172 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164566 | GGCGTGTGTTAGAGA[-/G]GGATTCTATTAGAAT | 286053 |
rs565290221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299969 | GACTACAGGTGCACG[C/T]CATCATGCTTGGCTA | 286053 |
rs565299625 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140385 | AATCATATAAAGGCC[A/G]GGCACAGTGGCTCAC | 286053 |
rs565315292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105032 | TGTCTCAAAAACTCC[C/T]TTGGATTCCTCCTCC | 286053 |
rs565316461 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125866 | GTCCCAAGTCCTACA[C/T]TGGTGAGGAAGGGCC | 286053 |
rs565327114 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260867 | GACCTCAGGTGATCC[A/C]CCTGCCTTGGCCTCT | 286053 |
rs565334770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111501 | TGCTTAAACCTTTCA[C/T]GTTCAAAATGTTTTG | 286053 |
rs565335601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337443 | TGGGCAATTATCTCT[C/G]TTGCTCAATTTACTT | 286053 |
rs565340008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330526 | GTGGAAATCTCCTGC[C/T]CTCTTGCCAATCCCC | 286053 |
rs565353634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306659 | AATTCCCAAGCCTTC[A/G]TATTGCACAGTGAAT | 286053 |
rs565365067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306236 | TCGGGAGGCTGAGGC[A/G]AGAGGATGGCTTGAG | 286053 |
rs565370457 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140486 | TGGCCAACATGGTGA[A/C]ACCCCATCTCTACTG | 286053 |
rs565375004 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154823 | CTGTTTTCTCAGTTT[C/G]ATATTGAGAACAGAA | 286053 |
rs565383846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104115 | CCTGCCTCAGCCTTC[A/G]GAGTAGCTGGGGTTA | 286053 |
rs565421591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360899 | TGCCTGAATTTTACT[A/G]TGCAAGCTTCAGGCC | 286053 |
rs565422364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248944 | AGAGGCTGAGGCAGG[C/T]GGATTACTTGTGGTC | 286053 |
rs565430950 | in-del | -/CAGT | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253927 | AAAAAAATTTTTTGG[-/CAGT]CATAGTCATCATGAC | 286053 |
rs565449081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337923 | AAGAAAGAAAACAAC[A/G]GGTTTGCCTGGAGAT | 286053 |
rs565464919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254233 | TTGAAGATGTCTAAA[A/G]ACAAAAGTCTTTTGC | 286053 |
rs565470406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357886 | AGGTGGCGTGTTCAC[G/T]CTAGAGGAAGAGGCA | 286053 |
rs565472980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125128 | CATCTGTGAATGGAG[A/G]TAGTTTTATTTTTTC | 286053 |
rs565477900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104468 | TGGAGTCTCTCTTGA[G/T]TGCCCCGAGGGTTCA | 286053 |
rs565491775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217523 | CTACCGCCACACATG[C/G]CTAATTTTGTTTTTT | 286053 |
rs565515032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128742 | CTAGCCATCTTCCAT[A/C]TTCAAACCTGGCAAT | 286053 |
rs565532168 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152479 | CAAGGGTGAAAACCA[A/C]TGACTTAAAAGAACA | 286053 |
rs565538469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198476 | ATTGGTTCTGTTTAT[A/G]TGATGGATTACATTT | 286053 |
rs565539747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314481 | ATTTTTAGTAGAGAC[A/G]GGGTTTTGCCATGTT | 286053 |
rs565544957 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124770 | GACATGAGCCACTGC[A/C]CCCAGCCTCCTCAGG | 286053 |
rs565552200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344472 | ATCATGGCCGGTCAC[A/G]GTAGCTCACACCTGT | 286053 |
rs565555632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217013 | GATGCAGTTATATAT[C/T]GCATCCATTTATTCC | 286053 |
rs565558748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301511 | GTGAACTTATTCACC[A/G]AAAGTACTTGGAAGA | 286053 |
rs565571395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148414 | TTTTGTAGCATTTTG[A/G]ATATCTTAGGCACAT | 286053 |
rs565576740 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283676 | CAAGACACATAAAGC[A/C]ATGCACAAATGAAAG | 286053 |
rs565593006 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170402 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTT]AAGACAGAGTCTCGC | 286053 |
rs565614302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209742 | TGTCTAACTTAATTG[C/T]TACCATGTGGTGAAT | 286053 |
rs565630399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294398 | TTTCCAAAAGGACTG[C/T]GCCATTTTACATTCC | 286053 |
rs565648755 | snp | C/T | 0.00173863 | 0.0294328 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155959 | CAGAGATTACTGTCA[C/T]ATATATTTAGCAATT | 286053 |
rs565666092 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249183 | CTCAAAAAAAAAAAA[A/T]AATAGGCAGAGCCAT | 286053 |
rs565669060 | in-del | -/TTAAC | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274266 | ACAAAAAAAAACTTT[-/TTAAC]TTATTTACTAAACAT | 286053 |
rs565673770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204307 | GCCTGTTTGTTGGAG[A/G]TGTTCCCAGACTTCC | 286053 |
rs565690099 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125351 | TTATTGAGAAAGCTT[-/CA]CACATCATTCTCACT | 286053 |
rs565691946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293963 | ATCTGTTAGCATTTA[C/T]TTCCTATTTTCTCCC | 286053 |
rs565706678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169625 | TACCTCCATTCCCAT[A/G]TTCACAGTCTTCAGT | 286053 |
rs565747171 | snp | A/C | 0.000847458 | 0.0205672 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118405 | AACAAACACACACAC[A/C]CAGAGATTGCTGGAC | 286053 |
rs565753199 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226140 | TTGATCTTTTTCTTG[G/T]CATATTAAACTGACA | 286053 |
rs565759970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155331 | CTGTGTAACTTTTGC[A/G]TGAAATGGAAGCATC | 286053 |
rs565765358 | snp | A/C | 8.2411e-05 | 0.00641862 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125357729 | GGAAATGAAGAAGCC[A/C]GTGAAAAATAAAGTG | 286053 |
rs565768546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164972 | AAGTAGTGAGGGATA[A/C]GTCTCCATGATAGAA | 286053 |
rs565769080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288105 | CACTGGGATTGTAGG[C/T]GTGAGCCACCATACT | 286053 |
rs565777294 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215454 | CATTGTTGGACATTT[A/G]GGTTGGTTCCAAGTC | 286053 |
rs565844912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176912 | ATTGGCCTGCACTTA[C/T]TGTGAGTTTCCTCAT | 286053 |
rs565884340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125619 | GACATTAATGATGAG[C/T]AGGCATTCCCTAGAG | 286053 |
rs565889753 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330800 | TTGCCTCCCACAAGC[A/T]CGTGGCCTGGAGCAC | 286053 |
rs565891524 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300208 | AAGTCTAGCTTGGTC[A/G]CCCAGGCTAGAGTGC | 286053 |
rs565912401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365351 | TCTATGGTCAAGCAT[A/G]TCCTGAAGCTGATCG | 286053 |
rs565912780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162855 | GGAAGGAAAAAGTGT[A/G]TAAGATTCACATTTA | 286053 |
rs565936906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356223 | TCTTCTCATTATGTA[C/T]GTCTGTGTGTATGGG | 286053 |
rs565939325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300983 | GTCCTGTCTGACTCA[C/G]TGACGTTCCATCCTA | 286053 |
rs565945723 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184740 | GTACCATGTCTAGTG[A/G]ATTTTCTTTCTTTAG | 286053 |
rs565951774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328754 | TCATTCATCCCTGTC[A/G]TCTGGGTCTCCACTT | 286053 |
rs565967652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352089 | AGTTATTCTTCATGG[A/G]TATTTTGTTAGGAGT | 286053 |
rs565986168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168901 | TCTAACACTGTTTGA[A/G]GTGCTTTATACACAT | 286053 |
rs565999619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257619 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 286053 |
rs566003081 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307429 | TGTGATTCTTTTCTC[C/T]GTGGCTGAACTTTTC | 286053 |
rs566004370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261981 | GCACACCTGTCATCT[C/G]AATTACTCGGGAAGC | 286053 |
rs566008685 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188340 | ACTCCAGCATGAGGC[A/C]TAGGTACAGTGTAGT | 286053 |
rs566009619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348870 | TAATACAGGAACCTA[C/G]GATTCAGCTTCCTGC | 286053 |
rs566018086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302931 | ACAAAGAATCTGAGC[A/G]CACATCATGCACCAC | 286053 |
rs566020721 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297132 | ATCTCTGTCATAATC[A/G]CACACCCATTTTTAA | 286053 |
rs566028534 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251219 | ATATACTACCCATAC[A/C]CATTAGAAAGTTTCA | 286053 |
rs566033724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172091 | AGAAATTGATTGTCT[A/G]AGTGGTGAAGAAACT | 286053 |
rs566049137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171513 | ATTCTTACCTATAAT[G/T]TTATTTGTTTGGGGG | 286053 |
rs566051376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366668 | GATTTTGACACTTTT[A/C]CTTTTTCAGTAAAAT | 286053 |
rs566054239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353610 | TCGTTTTAGGACGGG[C/T]GCAGTGGCTCACGCC | 286053 |
rs566058753 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115855 | GTGAAGAAAAGGGAG[A/C]TGTCATAGCCTACAA | 286053 |
rs566072151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235778 | TCCTCAAGAGCAGGA[A/G]TGGTTACATACTCAT | 286053 |
rs566079347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309108 | AAAATTTAGTTGGGC[A/G]TGGTGGCGCATCCCT | 286053 |
rs566080279 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294855 | TTACTGGATAATCCA[C/G]ACAGCACTTTGGTTA | 286053 |
rs566090464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235887 | ATGCTTGCCTTCTAA[C/T]CCCTAAGGAGTTATG | 286053 |
rs566101995 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245412 | TAAAAAAGAAACTTA[C/T]CTATAACACAAGTCA | 286053 |
rs566106221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282051 | GCAAATACCCTGTGT[A/G]GTGTTGCATCTTCCA | 286053 |
rs566109475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225731 | ACATGAGAGCAAATT[A/G]TACTTATTTGCTGAA | 286053 |
rs566121682 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309956 | TAAAGCTCTGCTGTG[A/G]GAAACTCAAGATCAT | 286053 |
rs566124097 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269611 | CATTCAATGATCATA[A/G]CTTTCTACAAGATCA | 286053 |
rs566125684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250413 | AAGATGTGTTATAGC[A/C]TATTAAGGTTAGACT | 286053 |
rs566129087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331620 | AATAACCAGATTCTT[C/T]TTATACACTTTTCTC | 286053 |
rs566144521 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347500 | TCCTACCAGACCCGA[C/T]CTTATTCCTCTTTGT | 286053 |
rs566145838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295524 | TGAGAGAATAACACA[C/T]AGGTCGGAATTCTCT | 286053 |
rs566166066 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270420 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCTG | 286053 |
rs566175717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180675 | GTTGGATGTAGAAGA[A/T]AAGTCATTTGACTTC | 286053 |
rs566186346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178606 | CTGGGCGTGGTGGCT[C/G]ACGCCTGTAATCCCA | 286053 |
rs566194257 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310627 | GCATACCTGCAAGTA[C/G]CTCATCCATTCTTCC | 286053 |
rs566199078 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345923 | CACTTTGGGAGGCCA[A/T]GGCAGGCAGATCACC | 286053 |
rs566203226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302399 | ATTCCAGGAGTGACA[A/G]GGAGGTTCCCATGGA | 286053 |
rs566209034 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098104 | AATCTACATTACCTG[C/G]AAATTTGTTAGAAAT | 286053 |
rs566216119 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309868 | CACTGAGCTAGAGCA[C/T]GATCTAATAAGATTG | 286053 |
rs566223180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227574 | ATCATCTTAATTGCA[A/G]ATGTATTGCAATTCA | 286053 |
rs566255691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187637 | TTTACCTGTTACGTG[A/T]CTATCAGGCCCTGTA | 286053 |
rs566257315 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142344 | TAGCATGTAATTTCA[C/T]AAAGCCTAGATTTGA | 286053 |
rs566285361 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126730 | CTGGCAATTATTAGC[A/C]TTGTGTAAGTTTTGG | 286053 |
rs566286362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289348 | CATCTTTGCGTTTGA[A/G]CATGTATTGCTAAGT | 286053 |
rs566289725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281733 | GACATGAGCCACCGT[C/G]CACGGCCGTAACTTT | 286053 |
rs566310018 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170857 | CTTCTGCTCCTCCTC[A/C/G]CCTAAAGTGGTTCTC | 286053 |
rs566310342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277317 | CTCCTCCTCAAGTCA[C/T]CTCTCTGAAGTCAAG | 286053 |
rs566330538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090188 | TTCCATGTAACAAAT[A/G]GAATTTCCATAATTT | 286053 |
rs566332837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326060 | CAGGAGATCGAGACC[A/G]TCCTGGATAACATGG | 286053 |
rs566340146 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316172 | AAACAAGTGAATAGC[A/T]TGTCTTCTTTTTCAA | 286053 |
rs566342953 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218432 | TTTTTTTTTTTTTGA[A/G]ACAGAGTCTTGCTCT | 286053 |
rs566364120 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290267 | TGTCTTAGTCAAAAC[A/G]TGACTGAAAGGAAAA | 286053 |
rs566390863 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172908 | GACGTTTATCTGACA[A/G/T]CACTTTAGACTGTCA | 286053 |
rs566392802 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125885 | TGAGGAAGGGCCCAG[C/G]GTGATACTGTGGAGG | 286053 |
rs566393268 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113714 | TTCATTTCCCCCGTC[A/G]TCCTCTCCTTTCTCA | 286053 |
rs566401554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315462 | GCTGAGTCATCTTGC[A/G]TGTCAAAACCTCAGT | 286053 |
rs566406290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227080 | GGCCACTCAGGGTCT[A/G]TATTAGAATTAACCT | 286053 |
rs566421030 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283097 | CAGTAAGTGGAAAGA[C/G]TAATAATATCTACAT | 286053 |
rs566425587 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221157 | ACAAAGTTTAAATAA[A/C]CAACCATGTCAGGTT | 286053 |
rs566434318 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348705 | TCTCTCTTGCCTGCC[A/G]CCATGTAAGACGTCC | 286053 |
rs566454105 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271154 | TAATCCCAGCTACTC[A/G]GGAGGCTAAGGCAGG | 286053 |
rs566469759 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228687 | CAGAGAGTCTGGTGT[C/G]TTACATGCCATATGG | 286053 |
rs566503856 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342483 | GGAGGATTTTAAAGG[A/G]ATGGAAAGTGGACAA | 286053 |
rs566505141 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101961 | TATTTTTTTCTCTTT[A/G]GAAAATTGCATCATA | 286053 |
rs566507105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333821 | CCCGGCCTTCCTGGT[A/G]GTTCTGATACCACCA | 286053 |
rs566518988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194261 | GTTGACTCCTCCCCC[C/G]ATTCCCAGCCCCTGG | 286053 |
rs566547601 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143933 | AGATTAGGGAGGATT[C/T]TGGAAAAGGACCTTG | 286053 |
rs566551005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135731 | CATGTAGGTATATAT[C/G]CATTTCTGGACACAA | 286053 |
rs566563979 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093421 | GGCCCTGGCACAGTG[A/G]CTTATGCCTGTAATC | 286053 |
rs566567475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142735 | CCAGGCTCCCGAGTA[A/G]CTGGAATTACAGGCA | 286053 |
rs566595830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208037 | GTAGAAAATACTGTG[G/T]CCAGATTGTCAGTCA | 286053 |
rs566597794 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239237 | GTCAAGCCTATCACC[A/G]TATTTGAGAAGAAAC | 286053 |
rs566647033 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339965 | TTCTTTAAATTTTGC[C/T]CCTGATCCTGGGAAA | 286053 |
rs566649106 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099697 | GACCTTGACAAGAGC[A/G]GTTGCAGTGGAGTGA | 286053 |
rs566654165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200486 | TTATTTTCTTTAAGA[A/C]TGTTGAATATCGGCC | 286053 |
rs566656810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238294 | CTCTCTTTCCTCACA[A/G]CAGTCCCAATAGCAT | 286053 |
rs566661031 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108857 | GAAATAAGACATATA[A/C]TTGTTATTCAATCAT | 286053 |
rs566676102 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150891 | AAGGGCACAGCCTGG[A/C]ACTCCTTAATACAAG | 286053 |
rs566724841 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311354 | GTAAAAAAAAATGCG[C/T]AAATTGTATAGTTTC | 286053 |
rs566725754 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157118 | GCATTGTGAATCATT[A/G]ACAAAAGAAGAAGGA | 286053 |
rs566728670 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094003 | GAGTTGGGGTCTTGC[C/T]GTGTTGCCCAGGCTG | 286053 |
rs566729277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207398 | TTAAAAAATCAGTTC[A/G]TCCCAAAGCTAGCAA | 286053 |
rs566729397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199485 | TTCCATGTAGTTGTG[C/T]GGTTTTAAATGAGTT | 286053 |
rs566731591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113930 | TGACAACTACTTTTA[G/T]GAATTTGATAGGATT | 286053 |
rs566740329 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205109 | ACTTTCACTCTTGCT[C/G]ATCTCTTCATGGACT | 286053 |
rs566744474 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205772 | GAGGGTTGAGAAAAA[A/G]TGGTTAGAATTATAG | 286053 |
rs566746496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106033 | GTATATGAATACATG[C/T]GTGTGTGTGTGCATA | 286053 |
rs566752255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149248 | CTGGATAGTAAAAGC[C/T]GAAGGGTCTTCTACC | 286053 |
rs566804584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327479 | GGGTTTGTCCCAAAT[A/G]ACTAAAATATTTTAC | 286053 |
rs566805313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213707 | TCTCTTTCCCTCCCT[C/T]CCTTCCTTCCTTCCT | 286053 |
rs566807819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106570 | GTAATCCGAGCTACT[C/G]AGGACTCAGGAGGCT | 286053 |
rs566809019 | snp | A/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171997 | TTAATGACCATGTTG[A/G/T]CTACTGTATTTTAAA | 286053 |
rs566814242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291353 | AAGAACTATATAAAA[C/T]TTTAATAAATTTAAT | 286053 |
rs566832901 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106006 | AGCCTGGACTTCTTA[G/T]GAACTCAATATGTAT | 286053 |
rs566847494 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260177 | TTTCAAATCAAGAAA[C/T]GTGGGAGGACATATC | 286053 |
rs566851083 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168583 | TGGCACCTTCTGGCT[A/G]TATCCTCACAAGATG | 286053 |
rs566853784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195677 | TCTATGCTCATGGAG[C/T]TTACATTCTGGCACT | 286053 |
rs566857949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252669 | TACATAAATGGGACA[C/T]CTTATAACTGAAGGA | 286053 |
rs566872288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298527 | CCAGTGCTGATGCTG[C/T]GCCTCATTAGCAGGA | 286053 |
rs566872727 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137804 | GTTCAAGGTACTTAA[C/T]CTCTCTGAGCCTGTA | 286053 |
rs566874272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145058 | TTTTGTATTATGTAA[A/G]TATTAGAGCACTTCA | 286053 |
rs566887977 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161148 | CCCAGTGAACTGTCC[C/T]TGGGAGAATGGAGAG | 286053 |
rs566911504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357525 | GGATCCGGGACTAAA[A/G]TCATGGCCTACAGGC | 286053 |
rs566945237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355471 | CTGGGAGGCCAAGGC[A/G]GGCAGATCACCTGAG | 286053 |
rs566966466 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227955 | ATTTCATGTTATGCA[C/T]GTGCCATTGATTTAT | 286053 |
rs566988468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246426 | TGACCTTGTGATCCA[C/T]CCGCCTCCTCCTCCC | 286053 |
rs566998522 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284133 | CACTCCAGCCTGGGC[A/C]ACAGAGCGAGACTCC | 286053 |
rs567013018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272870 | ACATATATATACACA[C/T]GTATACGTGTGTGTA | 286053 |
rs567020998 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198074 | GTTGCTTATCAGCTT[A/G]AGGAGATTTTGGGCT | 286053 |
rs567025486 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166591 | TTTTTTAAAATGGAT[A/G]CTTAGCAAGAACAGA | 286053 |
rs567032980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297708 | GGCATAATAGCGTGC[A/G]CCTGTAGTCATAGCT | 286053 |
rs567039403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094585 | GTTTGGTAGATACTT[G/T]CCATTTATACTGGAT | 286053 |
rs567045019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261002 | ATGCCATACATAAGT[A/G]TATTGGATGAAGCTG | 286053 |
rs567053250 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348959 | TCCCATGAGGAAACT[A/G]AGGTACAAAGCTGGA | 286053 |
rs567057847 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357031 | CCTCAGTTTCCTTAT[C/T]AAAAATAGTCAGAAT | 286053 |
rs567066435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115580 | ACACAGTGAAACCCC[A/G]TCTCTGCCAAAAATA | 286053 |
rs567081439 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342517 | GGGGTGGGTGAGAGG[-/A]AAGGAAGGCTTAGAG | 286053 |
rs567099270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362363 | TTCCAGCATCAACCT[C/T]GCCTCCAGGAAGTCT | 286053 |
rs567100780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271682 | ATGAATCAGGTTTCA[C/T]AGGCAGGAGCTCCTG | 286053 |
rs567101376 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114892 | CTTTAGGTAAATAAT[A/G]CTTGGACCTTTATTG | 286053 |
rs567107780 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216625 | GGCAACAAGAGCGAG[A/G]CTGTGTGTCAAAAAA | 286053 |
rs567111798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299379 | AGGCTGGGGAGGCCT[C/T]AGGAAACTTAAAATC | 286053 |
rs567117550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264468 | CTGGAATGCAATGGC[C/G]CGAGCTCGGCTTACT | 286053 |
rs567124024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168679 | GCCCTCGTGCTCTAA[C/T]CTCTTCCCAGAGGCC | 286053 |
rs567126645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123679 | TTTGCCGTTATATGT[A/C]GAGCTATTAAGTTTG | 286053 |
rs567126699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131613 | CTAACGTGGAAAAAA[A/G]AAATGCTTGGAGATT | 286053 |
rs567131900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259322 | TGTTAGGAACTGGGC[C/T]GCACAGCAGGAGGTG | 286053 |
rs567144677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350840 | ACCATATTAGGTTGT[A/C]AGGGACAGAGTCACA | 286053 |
rs567155457 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125130096 | CTTCTTAGTTGGTTT[C/T]GCTTTTTTTTTTCTT | 286053 |
rs567161971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173216 | TCAGTGGAGGTATTG[C/T]TGAGTCCCTTGGTGA | 286053 |
rs567178775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161812 | AAAAAAAAAAATCGG[A/G]AACGGTAACCAGAAA | 286053 |
rs567196079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258848 | CCTTGGTACAAGACA[C/T]TGTGGTCACACAACT | 286053 |
rs567202234 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199955 | TTGTCTCTTGATCTT[C/T]GTTGGTTTAAAGTCT | 286053 |
rs567206073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310022 | TTCTACTATGATGGG[A/G]GGACCCTCATCCTAG | 286053 |
rs567231116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306701 | AATTTATGGACTTTA[C/T]CTTGATATCCAGTCT | 286053 |
rs567232397 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266181 | ACCGCAACCTCCGCC[G/T]CCCAGGTTCAAGAGA | 286053 |
rs567236612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364060 | GTGATTTTCCTGCCT[C/T]AGCCTCACGAGTAGC | 286053 |
rs567251639 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215376 | GACATGAACTCATCA[-/T]TTTTTTATGGCTGCA | 286053 |
rs567267262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232336 | CCATTGCATTCCAGC[C/G]TGGGCAACAAGAGTG | 286053 |
rs567268938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253743 | TTAAAATGAAGTCGT[A/G]TAGGCAGCCTGATTT | 286053 |
rs567269744 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142057 | GAGCTAGGAAGATGA[-/T]TTTTCACTTGCTACC | 286053 |
rs567275646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202228 | GGGCTGCACCAGCTG[C/T]CCAACCAGTCCCAGT | 286053 |
rs567277852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209842 | ATAATAGCTCTTATC[A/G]TTTCATGTATTTTAA | 286053 |
rs567306248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176925 | TATTGTGAGTTTCCT[C/T]ATATCCTTGCTGGTC | 286053 |
rs567313229 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180934 | ATCAGACATCTTTCA[A/G]GGAGTTTATTAGGGG | 286053 |
rs567315362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272255 | TCCTGACCTCATGAT[C/T]CGCCCGCCTCAGCCT | 286053 |
rs567317958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343983 | TGCACACCAGCCTGG[A/G]GAACAGAGGGAGACT | 286053 |
rs567329831 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359139 | GGGCGTGGTGGCAGG[A/C]GCCTACAGTCCCAGC | 286053 |
rs567332205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300092 | CCAAAATGCTGGGAT[C/T]ACAGGCATGAGCCAC | 286053 |
rs567353522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280856 | TCATTATAAACTGGT[A/G]TAGTTAATCTGTAAC | 286053 |
rs567360236 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319122 | TCCATAATTCAGAGA[C/G]ATTGGTTACTTTTGC | 286053 |
rs567372085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177623 | CTGAGAGAAGCTTCA[C/T]GGAGCCATAATTCCA | 286053 |
rs567378417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278596 | GCGAACATGTTGATG[A/G]TATGGTAGAGGTGTT | 286053 |
rs567381104 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116909 | TTTTTTTTTTTTGAG[A/G]TGGAGCCTCTCTCTG | 286053 |
rs567382354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183344 | TTTGCAATCATGATG[A/C]GACTTTTGTTTTTAC | 286053 |
rs567408877 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307606 | TAGCTTGCCCTAGAG[A/T]TCTCAGAATACCTCC | 286053 |
rs567411623 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257577 | CTCGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 286053 |
rs567429753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279507 | AATTCAGTAGACTGG[A/G]GTAAGTAAGGTCAAG | 286053 |
rs567445298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184162 | AGTTTTAAGTAATTT[A/T]ATAATACAGGTTGAA | 286053 |
rs567456911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206658 | ATGGTGATACCATCA[A/G]AAAGTTGTAGACTGT | 286053 |
rs567473165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189417 | AAAGAAGGAGAGGAA[A/G]TTGCTTATGAAAGGT | 286053 |
rs567487478 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223901 | CACTATGCAGCCTTG[A/T]TGCAGAAATCATGCA | 286053 |
rs567494097 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307758 | GCAAGTGTCGTTTGC[C/T]CCCTGGAGGATGTGT | 286053 |
rs567498127 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166663 | TAGTTCTTTGATTCT[G/T]AAGATCCTCTAGTTG | 286053 |
rs567501246 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174721 | AAGGTGTTTCCATGT[G/T]TGGTTGGCTGCTACT | 286053 |
rs567508587 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159791 | ATGGTAAAACCCCGT[C/T]TCTACTAAAAATACA | 286053 |
rs567529146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188814 | AACCTGTTGGGTTCT[A/G]TTGAAAAAGCAGATG | 286053 |
rs567530594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138179 | CTAATATAGGAAGGG[A/G]GAGATCTGGCTTAAT | 286053 |
rs567537213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147470 | AAATGCAGATAAGAA[A/G]GGAAAGATTGGTGGT | 286053 |
rs567553887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312861 | GAAGAGTCATTAGAA[A/G]AAGCCTCTCTGAGGA | 286053 |
rs567559983 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211154 | TAATAACATTATTAT[A/G]TATGTATATTCTCTG | 286053 |
rs567589865 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181558 | ATTGGGGATGGAGGA[G/T]AACATGGGTTGAGAA | 286053 |
rs567605416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276489 | TTTTCTACTTGGCCT[A/G]CCTTCCTCCTATCAC | 286053 |
rs567611464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287448 | TTTCCACAGATGCCT[A/G]TCCTTGGGACATACA | 286053 |
rs567611536 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154199 | AATTTTCACATAGTC[A/G]TAGAAAGTTGATTTA | 286053 |
rs567613430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191260 | CAAAGAGATGTAATA[C/T]AAGTTGCCTAAAATC | 286053 |
rs567614565 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312170 | AATGAACTCTCTGAG[A/C]CATTTAATAAACTTT | 286053 |
rs567618436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274167 | GGAAGCTTAACCCGT[A/G]CTGCTTGGCAGATTG | 286053 |
rs567638235 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300062 | GACCTCAGGTGATTC[A/C]TCTGCCTTGGCCTCC | 286053 |
rs567671659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233993 | CATCCTGGCTAACAT[A/G]GTGAAACCCTGTCTC | 286053 |
rs567701770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323091 | TATGAAATACCTATC[A/G]ATGTATCTGACTAAA | 286053 |
rs567702394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169692 | TCTCCTATATTTCTT[A/C]TCTGGTAGCCCACGA | 286053 |
rs567717249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098809 | GGGGAGGGGTAGGGT[A/G]GGAGAGAAGGAATGT | 286053 |
rs567725927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097053 | TTGTATTTATATTGT[G/T]TAAAATGTCTCAACT | 286053 |
rs567731775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217594 | GATGGTCTGTATCTC[C/T]TGACCTCGTGATCCA | 286053 |
rs567738262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132547 | GCCCAGGCTGGAGTA[C/T]ACTAGTGCAGTCTCA | 286053 |
rs567753402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197937 | GATTCCTAGGTATTT[A/T]ATTCTTTTTGTAGCA | 286053 |
rs567753620 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091859 | GACGCAAGAGCCCGC[G/T]CTCACTTTTCAGCGG | 286053 |
rs567756427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268230 | CAAAGCAAGATGCTG[C/T]CTCAAGGAAGAAAAA | 286053 |
rs567775932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358281 | GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCACTG | 286053 |
rs567782660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198518 | TGTGTTGAACCAGCC[C/T]TGCATCCCAGGGATG | 286053 |
rs567790741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235905 | CTAAGGAGTTATGAC[C/G]TAGTAGGTAAGAGTC | 286053 |
rs567791006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285655 | ATAACAGCAACATGT[A/G]AAGACAGTACAAGAA | 286053 |
rs567795456 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314525 | TCGAACTCCTGACTT[C/G]GTGATCCACCCGCCT | 286053 |
rs567806865 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226236 | TAAATATTCTCATGG[A/C]CCAGTCATTGTGTAG | 286053 |
rs567807000 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328215 | CAGTCAGAATCATGT[C/T]CACAAGAAACAATAT | 286053 |
rs567835643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096397 | TCAAGAAACAGTCCT[A/G]GAAGTTTGCTATTGC | 286053 |
rs567836731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321407 | TACTGTTTTAAGGCT[C/T]TTACACTATAGAGCC | 286053 |
rs567837469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336509 | GGTTATATGCAGAGT[A/C]AGAAGCTATGAGAGG | 286053 |
rs567844207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199146 | AAAAACCTGGATTCA[C/T]TGATTTTTTGAAGGG | 286053 |
rs567864916 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293196 | ATTATACTCATGTCC[A/G]GGAAATAGGATGCTG | 286053 |
rs567874394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301521 | TCACCGAAAGTACTT[A/G]GAAGACTTTCTTGTT | 286053 |
rs567886951 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302325 | GTTAAAAGCATTGGG[A/G]ATAAATCAGAGGAAT | 286053 |
rs567900597 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147624 | TAATTTGGTATATAT[C/T]CTCAAAAAGGGCTTT | 286053 |
rs567901339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248497 | ATCTCTACTAAAAAT[A/G]CAAAAATTAGCTGGG | 286053 |
rs567930936 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214823 | GGGTGTTCGTGTATT[A/C]ACATTTATATTACAT | 286053 |
rs567934861 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288825 | TTTTGAGACAGGGTT[G/T]GCAGTCTCGCCCTAG | 286053 |
rs567935755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308388 | TTGGCAATTATCCTC[A/G]CCTAATGGTCTTCTT | 286053 |
rs567953709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193138 | ATAAATGCTTATGCT[A/G]TTAAGAGTTAACAGG | 286053 |
rs567954682 | snp | A/G | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090365 | TTAAGACTCAGCTAA[A/G]TCTTAAAAAACCACT | 286053 |
rs567957591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250251 | TGCCTTGGCTTCCCA[A/G]AGCCACCACGCCCAG | 286053 |
rs567959585 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184021 | AATTTTTCAATCTTG[-/A]AAAAAAAAAGATGCT | 286053 |
rs567981018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241073 | TATTGGCACTATTCT[C/T]ACGGGTTGAATATCC | 286053 |
rs567983005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197232 | CTATTTTGGCTTTTG[C/T]TTCCATTGCTTTTGG | 286053 |
rs567997845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103634 | AGATGGGTTGATATT[A/G]TCCCATAAATCAGTG | 286053 |
rs567998336 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295241 | TCTCTTTACCTTCTG[A/G]GGCCCCTAATCTGGT | 286053 |
rs567999977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337131 | TATATTAGGTTTCTG[C/T]AGTCTTGAGGTACGG | 286053 |
rs568011259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302103 | CTGGGATTACAGGTG[C/T]GTGGTACCACACCCA | 286053 |
rs568047405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243018 | ATATTGGTTACATGT[A/G]GACTCTATCTGGGTA | 286053 |
rs568078104 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212194 | TCAAACTCAGGCTCT[C/T]TGCTACCGACTTTTA | 286053 |
rs568082024 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288281 | ACTGCTTCTCTGACT[G/T]CTGGGACGTAACAGG | 286053 |
rs568096241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257677 | TAGCTGGGACTACAG[A/G]CGCTCACCACCATGC | 286053 |
rs568099742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243518 | AAAAAAAAAACCTCT[A/G]AATTTCTAATGTGTA | 286053 |
rs568104085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355006 | GGCTATGTGTGTAAG[A/C]TTTATATGAAACATA | 286053 |
rs568119052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324189 | AAAACTGATCATACC[A/G]TGTGTTGGCAAGTCT | 286053 |
rs568135726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163582 | CAATTGTAGATAAAA[C/T]GAGATTGTAGATAGG | 286053 |
rs568150329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112164 | AACTATACCAGCAAA[A/T]TAGCATTATAACTTA | 286053 |
rs568161346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105605 | GTTGGCAAAGTTTTT[C/T]TATAAAGGGCCAGAT | 286053 |
rs568177635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192231 | GAGTTATAATTCCTG[A/C]AGTTAGAATGATTTA | 286053 |
rs568183162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218270 | TTATTCTACAGATAA[C/T]GCTGAGGATTCTGAC | 286053 |
rs568191567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352207 | AATTTGGGGCTGGGC[A/G]TGGTGGCTCACGCCT | 286053 |
rs568237347 | in-del | -/AGG | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121525 | ATCCATGCAAAGATC[-/AGG]AGAACTACATGGTAG | 286053 |
rs568238197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352626 | ACCTACACTTTCTTT[G/T]TATCTCAATTGTCTC | 286053 |
rs568245330 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262582 | ACACTAGGGTAGCAA[A/G]AATAAATAAGACAGT | 286053 |
rs568273602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170609 | GATGGGGTTTCACCA[A/T]GTTGGCCAGGCTGGT | 286053 |
rs568302880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249358 | TTGGATGATAGCATC[C/G]CCACATCACAGCTGA | 286053 |
rs568306264 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211694 | TTTATTAATCTACAA[A/C]CCCATCAACAATGTA | 286053 |
rs568307099 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240568 | TATTCTGCCTTTCTG[A/C]ATTCTTTTTCTGCAT | 286053 |
rs568309394 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301965 | CCGCACCTGCCCCAA[-/T]TTTTTTTTTTTTGAG | 286053 |
rs568318928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256895 | GCCACTGCACTCCAG[C/T]CTGGGCGACAAAGCA | 286053 |
rs568320549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120587 | TACGATATTGGGCAA[A/G]CCAGAGGTTAAGCCT | 286053 |
rs568326651 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227591 | TGTATTGCAATTCAT[A/C/G]TTAAAAATCAGGAAG | 286053 |
rs568326893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126385 | CAAAAAAAAAAAAAC[A/G]AGGGGGACAGTTATT | 286053 |
rs568370077 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111694 | AATCCCAGCTACTTG[A/G]GAGGCTAAGGCACAA | 286053 |
rs568372343 | in-del | -/GGTGAAACCAGCCTGGTGA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106486 | GTTTGAGACCAGCCT[-/GGTGAAACCAGCCTGGTGA]GACCAACTTGGTGAA | 286053 |
rs568376031 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180009 | ACATCTTAGGTGGAT[G/T]TGAGTCCATTTTATT | 286053 |
rs568388953 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119233 | TTTTCTTTCCTCCAC[C/T]GACTGTAACAACCTG | 286053 |
rs568399920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296217 | ATTTAGTGTTGTCAT[G/T]TGCAGTTTGCACCCT | 286053 |
rs568406817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263798 | TATGACCTAGAATAA[A/G]TTTAATCTGGGACTA | 286053 |
rs568416891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165914 | ATTATAGAGAAAGCA[A/G]TGCCAGAGAATTTGA | 286053 |
rs568430088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360641 | GGGCAGGGTTCTGAA[G/T]GCCAGGTGCATTTGG | 286053 |
rs568430623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340828 | CTCACAAGGTCTTTC[C/T]AACAATTAAAATTAT | 286053 |
rs568431846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252266 | GGGCACAGTGGCTCA[C/T]GCCTATAATCCCAGC | 286053 |
rs568433135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114616 | ACAACTCGGGGATGC[C/G]GGGAGCATGTGTGCC | 286053 |
rs568433492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347630 | CTCAAAGAGCTTTCA[A/G]TGTATCAGGAAAAGA | 286053 |
rs568468027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158475 | AGAATGGGCAGGAAA[C/T]GCATATGGACCTTTG | 286053 |
rs568470391 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267043 | AGAGTCTTGCTCTGT[C/T]TCCCAGGCAGTAGTG | 286053 |
rs568470426 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199982 | GTCTGTTTTATCCGA[A/G]ACTAGGATTGCAACC | 286053 |
rs568473743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165182 | TAAAAAGAGAACAGT[C/G]ATACCTCATAGGGCT | 286053 |
rs568487576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113979 | AACCAAAAGAAGTAA[A/G]TTCCCAGTTATTAAG | 286053 |
rs568491123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310519 | TCAATATGGTTTTCA[A/C]AATAAAGACCAATAT | 286053 |
rs568551323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173974 | TGAACCACTCAGACG[A/G]AAGGTGCTGTGTAAG | 286053 |
rs568557456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277872 | AATCATAGAAAACTG[C/T]AAATTAAATGAATAA | 286053 |
rs568563360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180069 | CTTTTCTAAGAACCA[A/G]CAATTTATTTTCTAG | 286053 |
rs568570604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325323 | AATAAAATAAAATAA[A/G]GTAAAATAAAATAAA | 286053 |
rs568582435 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213323 | TCACATTATTAATTG[C/G]ATTCTCTCTTGGCCA | 286053 |
rs568593674 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304486 | ACAGCAAGTAGTTAC[A/G]ATGGTTTAGACAAAG | 286053 |
rs568612206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205803 | GTTGTAAATACCAGT[A/C]TCGTACTTAATAAAA | 286053 |
rs568613281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185838 | TTTACATTTTTGTCA[A/G]TCTCTTCAATTTTTG | 286053 |
rs568614914 | in-del | -/TAATAATAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275028 | TAATAATAATAATAA[-/TAATAATAA]ATAGAATAATATCCT | 286053 |
rs568620587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270073 | TAAGGAGCTATAAGA[A/G]GAGAGAGAGTGTAGC | 286053 |
rs568643906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220054 | GAAAGGCAGACCAAA[C/T]CCACCCATGGGATTT | 286053 |
rs568646311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171613 | AGCTGCTGCTACTAA[C/T]ACTGCTGCTAATTCT | 286053 |
rs568663494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143836 | ACACATACACACACA[C/G]ACACACATCCACGTG | 286053 |
rs568682300 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283754 | GCCCTCATGACACAG[C/G]ACAGTCAACATGTAG | 286053 |
rs568707272 | snp | C/T | 0.115088 | 0.210473 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316772 | TTCCTTCCTTCCTTC[C/T]CTCTCTCTCTTTCTT | 286053 |
rs568713917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275915 | TCCAATAACTCTGTT[A/G]TGTCTTTAGCCCGAC | 286053 |
rs568728079 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138880 | GAGGACCAGAATTTA[C/T]AGCCTGCTTCTGATA | 286053 |
rs568739511 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235340 | TCATATCTATTTGCC[C/T]TTGAGCATATATTTC | 286053 |
rs568756358 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310017 | CTCATTTCTACTATG[A/T]TGGGGGGACCCTCAT | 286053 |
rs568793249 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141913 | CAATAAGCATTTGCC[A/G/T]GGCAAATGAGTTTCT | 286053 |
rs568822229 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210220 | TCAATGAATTTATAT[A/G]TGAAAGTCATTTGCA | 286053 |
rs568837673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144819 | TATAACACAAAATCA[C/T]CCATTTCTGTTTAAT | 286053 |
rs568838877 | snp | C/G | 0.0310518 | 0.120672 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129574 | TGTGTGTGTGTGTGT[C/G]TGTGTCTGTGTGTTT | 286053 |
rs568876310 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173411 | GAGAAACAATGTTTT[C/G]TATTATTCACTGGTT | 286053 |
rs568887314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188273 | TCAAAACCACAGTGT[A/G]GTTGCACAAGGGTAG | 286053 |
rs568900564 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311413 | AATCTTATTTTTACC[C/T]TGGACTTTCAAAAAC | 286053 |
rs568914919 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154777 | CACAGATACACACTT[C/T]TTTTTAATCACTATT | 286053 |
rs568917745 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311938 | CCAGGCATGGTGGCG[C/G]ATGCCTGTAATCCCA | 286053 |
rs568926082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258924 | TTTCTGTTTTTGAGA[C/T]AGAGTTTTGCTCTTG | 286053 |
rs568946536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187757 | CTTTCAAAATATAAG[A/G]GCTTTGCTTTATGTT | 286053 |
rs568947941 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252875 | CCGGAAAGAGCCAAG[G/T]TTATTTAAAGTGTCC | 286053 |
rs568957870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363172 | CACAAAAGTGTCTGT[A/G]TCCTCTTCATGATCT | 286053 |
rs568968095 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203344 | TGGACCTTGCATAAC[A/T]AATATCTAGAAAGAG | 286053 |
rs568969907 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164846 | TAGCAAGCCTAGCTA[A/G]CATGTCTCCAGTGCT | 286053 |
rs568971031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136496 | TGGTTCTGTTTGGTT[A/G]CAGAGACTAGGTGCC | 286053 |
rs568973804 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195702 | GGCACTGACCATCAA[A/C]CCACTTTACAGTATT | 286053 |
rs568975125 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236350 | GGATTAAATGTAAAA[-/G]GACGAGTTGCAAAAC | 286053 |
rs568976531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125130136 | ACAGTTTTGAGGAAT[A/C]CTGCTTAGGTGTTTT | 286053 |
rs568979839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320036 | TAAAAATTAGCTGGA[C/T]GTGGTGGCATGCACT | 286053 |
rs568980563 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318840 | ACAGGGAAGGGGAAC[A/C]TAGGCAGATCCTTGT | 286053 |
rs568986891 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137785 | TTATTACTATATGAC[-/T]TTAGTTCAAGGTACT | 286053 |
rs568996011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355566 | TTAGCCAGGCATGGT[A/G]TCGTGCACCTATACT | 286053 |
rs569005105 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290409 | TCTAAAAGGAGGCCC[C/T]TTTGGTCTTTCTCAG | 286053 |
rs569012409 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340168 | TACAGGCGCCCGCCA[C/T]CACGCCCGGCTAATT | 286053 |
rs569015207 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341424 | GTCCCGCTTACAACT[G/T]CAGGTAGTATGTACA | 286053 |
rs569020635 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222192 | GCTTTTTAAAAAGAT[A/T]AGGTATAAGGATGTC | 286053 |
rs569035009 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131931 | TTCCAGAATTCAAAT[C/G]TGGGCAGCCTGTCTC | 286053 |
rs569048530 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232219 | TACAAAAAAATCAGC[C/G]GGATGTGGTGGTGCA | 286053 |
rs569065599 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298643 | ATACCATTGAACGTG[A/T]CCAGTGGTTCTTAAC | 286053 |
rs569070174 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093461 | TGGGAGGCCAAGGCG[A/G]GCGGATCACTTGAGG | 286053 |
rs569077710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303584 | TCTGCACCCCCTCTC[A/G]CTGTTTAGGAAAAGG | 286053 |
rs569080932 | snp | A/C | | | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102024 | TGTAGGCTTTTAAGA[A/C]CTGTGCTATTGTTGA | 286053 |
rs569087242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194334 | CAGAATGTTGTATAG[A/G]TAGAATTGTACAGTG | 286053 |
rs569107519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238146 | AGTCCCCTCCTAACC[C/T]GGGTCTCTCTTGAGA | 286053 |
rs569108537 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106955 | GAGCCGAGATCACGC[C/T]ACTGCACTCCAGCCT | 286053 |
rs569110160 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201840 | TTGATGAGCTGTGGT[A/G]GGCTCCCCCAAGTTC | 286053 |
rs569110652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093894 | CTTGGACTCCTGGAC[C/T]CAAGGAGTCCTCCCA | 286053 |
rs569112820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352700 | AAACTTCTGTGATTC[C/T]AGTAGATGATCAATA | 286053 |
rs569128671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304991 | AAGGAAAGAGGGAGG[C/G]AGGGAAGGAAGGAAG | 286053 |
rs569141544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200577 | TCCCTTTGTGGGTAA[A/C]CTGACTTTTCTCTCT | 286053 |
rs569147805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229574 | CGACATTTGAAGATG[C/T]TTCATACAAAGTTGG | 286053 |
rs569160772 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239394 | TGGGCAGATCACTTG[A/T]GGCCAGGATTTCGAG | 286053 |
rs569177904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334600 | ATTGTTTTTCTCACG[A/G]GTTGGAATGTAGCAA | 286053 |
rs569185040 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225263 | ATGCCAAGAAACAAA[C/T]TAGCTAAAAGTAAGG | 286053 |
rs569199673 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227434 | CCCCTCCAGAGCCAC[A/T]GCTTTGCTGCCTTAC | 286053 |
rs569203895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286085 | GAGAGTTAATTTGCA[C/T]ACCACTGTCAATACC | 286053 |
rs569207050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326120 | AAATTAGCTGGGTGC[A/G]GTGGCAGGCGCCTGT | 286053 |
rs569209340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299204 | TGAGGTTATCAATAG[C/T]CTAGTTGATACAGGA | 286053 |
rs569214841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333756 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 286053 |
rs569224166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189449 | TAAGGCTAAAACTTG[C/G]CTGGGCCTGTCCAGA | 286053 |
rs569249282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138733 | ATGATTGTTATTTAT[C/G]CTGGGAAGCAAAGAT | 286053 |
rs569265726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292115 | ACCTACCTACAAGGA[A/G]GGCTGGACAAAGGTA | 286053 |
rs569270880 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154203 | TTCACATAGTCATAG[-/A]AAGTTGATTTAAAAA | 286053 |
rs569271027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247107 | CTGAGTGGGGCAGGA[C/T]TGCTTGAGCCCAGGA | 286053 |
rs569283658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188933 | AGGTATGTGTGAGTT[C/T]TGAAACTTGGAAGAA | 286053 |
rs569301552 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111597 | TTGAGGTCAGGAGTT[C/T]CAGATCAGCCTGGCC | 286053 |
rs569305518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352022 | CCATTTCAAAAATAT[A/G]TATACATAGTGGGGC | 286053 |
rs569306363 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | NSMCE2 | GRCh38.p7 | 8:125102114 | ACACTTACCTTCCCC[A/G]TATATTGAGTCCAGC | 286053 |
rs569309846 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356704 | GATAAATATAACCCA[C/T]ATAGAAAAAGCTTAA | 286053 |
rs569319873 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134904 | AGCTAATGAAAAATA[A/C]ATTTTGTTTTGTTTT | 286053 |
rs569343493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351413 | CATCCCTCATGGGTG[C/T]GCTGTAAATGTTAGT | 286053 |
rs569347300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358130 | CTGAGGTCAGGAGTT[C/G]AAGACCAGCCTGGCC | 286053 |
rs569349406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146902 | AAAGTATAAAAAAAA[A/C]AAAACAAAAAAAAAC | 286053 |
rs569374207 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354834 | CTGCCCCTCAGTACA[G/T]CTTGAGCATCCCTAA | 286053 |
rs569378687 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248597 | GGCGGAGGTTGCAGT[A/G]AGCTGAGATCACACC | 286053 |
rs569381248 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235359 | AGCATATATTTCTTA[-/AT]ATGTTTTCTTCCTAA | 286053 |
rs569381355 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279199 | TGATAGATGTGGTTC[A/C]GTGCACCTGGGAGCT | 286053 |
rs569386751 | snp | A/G | | | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125129859 | GATAGTGGAGTTCCC[A/G]TATACCCATACCCTC | 286053 |
rs569402063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096714 | CTCCAGGATTCAAGC[C/G]ATTCTTCTGCCTCAG | 286053 |
rs569408196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160298 | TTGCCTAGAACGTTC[G/T]GTAAAGAACTCATTT | 286053 |
rs569424828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109047 | GAGGAGATTATGTCA[A/G]TAGCTCAAGTGAAAA | 286053 |
rs569427770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207512 | TTTTCAGTGGCTGTA[A/G]TTCAAAACTGCTGTG | 286053 |
rs569458408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342543 | TAGAGGCAAGGACTT[C/T]GTTCTACGATGCTGA | 286053 |
rs569462301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159421 | ATACATAAATAGTTG[C/T]CATGTTACAGTTGCC | 286053 |
rs569476406 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364959 | AATCTACCAAAATTT[C/G]GTTCACTTTGAGAAC | 286053 |
rs569477040 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223844 | TGAGTCAGGGTCTTG[C/T]GCTGTCACGCAGGCT | 286053 |
rs569478982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108274 | GTAATTCAGCAAGAA[C/T]TTGTTAGGGGAGCAG | 286053 |
rs569500773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343224 | CAATCTGAGGACAGC[A/G]CTGAGCACTAACAGA | 286053 |
rs569509769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152526 | AGAAAGTCAAGTGTT[C/T]ACTGCCAAAGATTAG | 286053 |
rs569520636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116992 | TCCTGGGTTCAAACA[A/G]TTTTCCTGCCTTAGC | 286053 |
rs569523880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162750 | ACCACAGGCTGATTT[A/G]AATTGGTGAACTCCT | 286053 |
rs569530402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253420 | GCAATCTTTGTGGAT[C/G]GGTGTTTGGGGAATT | 286053 |
rs569533565 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167517 | TAAAAATACAAAAAT[A/T]AGCTGGGTTCGGGAG | 286053 |
rs569535790 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122404 | ACCTTCTACAACTAT[A/T]TTAAACCCTTGAGCA | 286053 |
rs569538354 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115610 | ACAAAAATTAGCCAG[A/G]CATGGTGGCAGATGT | 286053 |
rs569544241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344085 | GAAATGGTGTCATAG[C/T]CCCATCTTACCCAAA | 286053 |
rs569544977 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274802 | AGGCATGGTGGCGCA[C/T]GCCTGTAATCCCAGC | 286053 |
rs569552593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203345 | GGACCTTGCATAACT[A/G]ATATCTAGAAAGAGG | 286053 |
rs569570541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307375 | CAGCCAGCCATCGTG[C/T]TGTCTGTTTCATAAT | 286053 |
rs569574107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208097 | TTGAATACTCAAATA[C/T]GAGTTTTTAACTGCT | 286053 |
rs569575260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350652 | CAGGCAAAGAGAGAG[A/C]GAGCTTGTGCAGGGA | 286053 |
rs569587224 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155120 | GCGAAGTCCAGAACA[G/T]AAGACAAATATTTTA | 286053 |
rs569601063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216659 | AAAAAAATGGTCTAT[A/G]GGTTTTGGGCAAATG | 286053 |
rs569606390 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154401 | CCTTTGGCAATTAGC[A/G]GAAGTTCTCAGGTTA | 286053 |
rs569628479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300945 | ATCCTACCTAACCAG[C/T]GGTCATCTCAGTTCC | 286053 |
rs569630596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293246 | GGATCTTGTCCATTA[A/G]TCCACACTGGAAGTT | 286053 |
rs569656784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124469 | GTGGATTCCTCAGGA[G/T]TTCTCTCTCTCTCTC | 286053 |
rs569664454 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355157 | TCAACCTGTAGTGCC[-/T]TTTGCAAACAAACAC | 286053 |
rs569666618 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299554 | CAGCCCCCATGACCC[A/G]GTTACCTCCCACCAG | 286053 |
rs569666655 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270788 | CTAAGGAGGGGTGAA[C/T]GGGCCCAGGTTGAAA | 286053 |
rs569689948 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210804 | CTGCTCACTGCAACC[A/T]CCACCTCTGGGGTTC | 286053 |
rs569693639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170768 | CTCTCACTGTTTCTC[C/T]TACTGTCACCCTAAT | 286053 |
rs569699793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216272 | TGCTGTGAGCATCAG[G/T]GTACATGTATCTGTT | 286053 |
rs569701168 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200865 | TTCTTGGAGGCTTTG[-/T]TTCTTTTTACTCTTT | 286053 |
rs569702710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337282 | TGACTTGCAACCCTA[C/T]ACCCCCTCTAAGTCT | 286053 |
rs569728006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297169 | GTATTTCATATTTTC[A/G]TGCTTTTTAGTCAAG | 286053 |
rs569732919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220557 | CATAAATTGTGTTTC[A/G]TATTACAACTTGTTC | 286053 |
rs569739774 | in-del | -/ATGTAG | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276523 | TGTAGAATAATTAAT[-/ATGTAG]AATGGAATAGCCTCA | 286053 |
rs569754769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171368 | CTAGGGTTAGTAGTA[G/T]GTCATGGACTTAGCG | 286053 |
rs569756587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163642 | AATTGAAAGGTGGTT[A/G]TATAGTTACCACATA | 286053 |
rs569758263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312948 | CACAGAAAGCACATA[C/T]CACATGCAAAGGCCC | 286053 |
rs569793592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301676 | TTTTTTTTTTTTGAG[A/G]CAGAGTCTCCCTCTG | 286053 |
rs569793644 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209305 | ACAAAAGTAAGGAAA[C/G]CCCCATTGAGTGATG | 286053 |
rs569794146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364678 | CCAGAACTTTAAAAC[C/T]TCTTGGAAGAATGAT | 286053 |
rs569799244 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364120 | GGCTAATTTTTGTAT[C/T]TTTAGTAAAGATAGG | 286053 |
rs569823040 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278903 | GATTCAACTCAAACC[A/G]AGAACCAGGATGGGA | 286053 |
rs569830508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269744 | TGCAGAGGATAACTT[A/G]CTTCACATGAATCTC | 286053 |
rs569851282 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306975 | TAGAGTAAGCAATTT[A/T]TAAAGGTTCAATGTT | 286053 |
rs569864200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183164 | ACATAAATTTACCTC[A/G]TGTCCTTATATGTGC | 286053 |
rs569870156 | in-del | -/TTTA | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140166 | TTTTTAGTCATATGC[-/TTTA]TTAATTTTAAAAACA | 286053 |
rs569875470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140452 | AGAATTACTTGAGGT[C/G]AGGAGTTTGAGACCA | 286053 |
rs569883159 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277413 | ACAATTTTAGAGATC[G/T]CAAAAGAAAATGGCT | 286053 |
rs569885950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261059 | AGAAAAGAAGCCTCG[A/G]TATTTACATTTCGGT | 286053 |
rs569903890 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147986 | TCTCTGGTCTCTCAG[C/T]CCCCTGCTACAGCTG | 286053 |
rs569905492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168740 | AGGATTTCATCATAT[G/T]AATTTGGAGGGCACA | 286053 |
rs569911248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131639 | AGATTGTAAGTACTT[A/G]AGAGGAGAGATTATG | 286053 |
rs569912547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366583 | CATATCGCTTGTGTC[C/G]CCAGCACCCAGACAG | 286053 |
rs569912951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280093 | CTCACTGCCAAGAAA[A/G]TGATGATTTTCTTTA | 286053 |
rs569917543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306709 | GACTTTATCTTGATA[C/T]CCAGTCTTCATTTTG | 286053 |
rs569927689 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152672 | TATTACAGATAAGAA[A/G]ACAAGATTTTGGAGT | 286053 |
rs569950385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267259 | TTGATCTGCCTGCCT[C/T]GGCCTTCCAAATGCT | 286053 |
rs570007079 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263251 | GAATATAAATCATTA[C/T]CTAATTGCCATTTCC | 286053 |
rs570009623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185039 | GAAAATAACCACCAT[A/G]TCTTCACTAACTTTA | 286053 |
rs570012116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147728 | ATCAGTACCTCCACA[A/G]CCACCCCAACCCCCA | 286053 |
rs570022622 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217894 | TGAAAAAAAAAAAAA[-/C]CAAAACAAAAACCGT | 286053 |
rs570024548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274485 | CAGTTAACTCCATGT[A/C]ACCTACCAGTTTTCA | 286053 |
rs570035089 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309034 | TGGATCACCTGAGGT[C/G]AAGAGTTCAAGACCA | 286053 |
rs570035331 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134170 | TTGTTATGTAAAAAA[C/T]CTGTATTGATGAATG | 286053 |
rs570069062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177727 | TTGCATCATTTTCCC[C/T]AAAGGACAAGCACTT | 286053 |
rs570078378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227004 | CCAGCCCCCTTTGCC[G/T]AGGGACTCACCAGTG | 286053 |
rs570092458 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304754 | CCCAGCTGCTTGGGA[A/G]ACTGAGGCATCAAGT | 286053 |
rs570107359 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092562 | GTGCATGTGATAGGG[A/G]TAATGGTAGCATGAG | 286053 |
rs570125051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288014 | TTTTTCTTGTGGAGA[C/G]AGGGTCTCGGTATGT | 286053 |
rs570148309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262653 | CAATGCTTTTAGCTC[C/T]ACAATCTGGTGTCAT | 286053 |
rs570151503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218672 | CCGCCTCAGCCTTCC[A/G]AAGTGCTAGGATTAT | 286053 |
rs570174667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308440 | TTTGACCTTTTCCAT[A/G]GTAGCATTTTACGCT | 286053 |
rs570177923 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199864 | TCTGGGTGCGCCTGT[A/G]TTGGGTGCATATATA | 286053 |
rs570179678 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316783 | CTTCTCTCTCTCTCT[C/T]TCTTTCTTTCTTTCT | 286053 |
rs570179965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325980 | TAAATAAAAATACCC[A/G]GGCGCGGTGGCTCAT | 286053 |
rs570188424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352804 | GATATTTATTGCCAG[A/G]TGTGACCTTTTGTTA | 286053 |
rs570196124 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110630 | AGTAGGGATTTGATT[A/G]TAAGCAGTCTGACTT | 286053 |
rs570205902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116198 | TGTAATATGAATTCT[A/G]TTTTACAAATGACAA | 286053 |
rs570223830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184320 | TATAATTCAAAAAAA[A/T]GATAAATGTTGAAAT | 286053 |
rs570235804 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145316 | CACTGGCATACTTAC[A/G]GAAACAGCTAGAATT | 286053 |
rs570237821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183038 | CTTTTAGGATTGAGA[C/T]GCTTGTATTTCTTAA | 286053 |
rs570239659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193715 | AACAAAACAAAAAGC[A/G]TATTTCTTCTTCTAA | 286053 |
rs570252264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133599 | ACACAAAATTAGTGA[A/G]GCATGGTGGCTCGCA | 286053 |
rs570257892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090127 | AGAAGGAAATCACTT[A/G]GTTACATTTTATGTA | 286053 |
rs570263381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281552 | TCAACCGATTCTCTT[A/G]CCTCAGCCTCCTGAG | 286053 |
rs570278971 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221664 | CATAATGAAATATAT[C/T]AGGGATAAGACCCAA | 286053 |
rs570294018 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091140 | GAACTTTTTTTTTTT[C/T]CCCCAAATGCAAAGG | 286053 |
rs570315571 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199287 | AGGGTGTCGATTTTA[C/G]ATCTTTCCTGCTTTC | 286053 |
rs570327874 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197993 | TTTGGGTCTCTGTCT[A/G]TTATTGGTGTATAGG | 286053 |
rs570328354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282959 | GGAAGGTAGTCTAGC[A/C]TAATTGTTGAAAGAG | 286053 |
rs570333838 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302339 | GGATAAATCAGAGGA[A/C]TCAGTCCTTGCAAAG | 286053 |
rs570333975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323270 | CAATCAGAATCCCAG[C/T]AGGGGTTTTTTTGTA | 286053 |
rs570336611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332457 | GTGAATAATATAGTA[C/T]TCGCATCAGAGTTGT | 286053 |
rs570345254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186819 | AGTATTTACCATCCC[C/T]AGAATACAAACCTAA | 286053 |
rs570367077 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234105 | GGCTGAAGCAGGAGA[A/G]TGGCGTGAACCCAGG | 286053 |
rs570372625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097308 | TTGAAAATACATAGA[A/G]CTCAAATTTCCATGA | 286053 |
rs570388605 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191390 | TTTCTCTCAATTCAA[A/G]CATACCATTCATTTC | 286053 |
rs570394278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322376 | AAGAAGGAAAATCAT[A/G]TGATCATCTCAATAG | 286053 |
rs570400991 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306438 | CCAATTTAAATTTCT[C/G]TATCTCTCTCTCTCT | 286053 |
rs570421052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098860 | TTTAAGTTCTGGAGT[A/G]ATCTTGCCAATGGTA | 286053 |
rs570424623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142678 | GGTGCTATCTTGGCT[C/T]ACCACAACCTCCACC | 286053 |
rs570430979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228631 | ATTCAGAGCCAAAGA[C/G]GGCTGAGAGCATATG | 286053 |
rs570447233 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327607 | AGACAAGAGAGAGGG[G/T]AGGTACAGAACTAAG | 286053 |
rs570454186 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239842 | CAAGATTCCTGCTAA[C/T]AGAAAAGTATATAAC | 286053 |
rs570477378 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322991 | TGAACCCAGGTTTCG[-/T]GAGGTTGCAGTGAGC | 286053 |
rs570491998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236531 | AATGGAAATGTTTGC[A/G]TATGTGTGTTTCATA | 286053 |
rs570500989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251699 | AATAGTTATTTTCAT[A/C]ATTAGCTGACTTCAT | 286053 |
rs570511550 | snp | G/T | 0.00159617 | 0.0282053 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367551 | AAAAAAAAAAAAGAA[G/T]GTCTTTCAAGTGATA | 286053 |
rs570512838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348868 | ACTAATACAGGAACC[A/T]AGGATTCAGCTTCCT | 286053 |
rs570513471 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346886 | ACATGTCTGCAACAA[C/T]AGTAGATAAATTATA | 286053 |
rs570547398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348273 | TATTGGATCCTTATT[A/G]TGTTCTAGCCATTTT | 286053 |
rs570548146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105879 | TGGATTAATTTTACA[A/G]CAAATACTTGATTTT | 286053 |
rs570580466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245759 | AAATATGAAGGCCAG[C/T]TCTGTGGCTCACGCA | 286053 |
rs570588693 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126370 | GTGAGACTCTGTTTC[-/A]AAAAAAAAAAAAACG | 286053 |
rs570627760 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278776 | TGAAATTCACTTCCA[C/T]CTGTTCAAAAATTGC | 286053 |
rs570631882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212273 | TTTATGACCTGTTTT[C/G]TGGTAGCCCAGGATA | 286053 |
rs570641446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244961 | ATAAGATTTATACTG[G/T]CCACAAAGTGAATTT | 286053 |
rs570643559 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107144 | TGAATAACCATAGTT[A/T]GTCTGTGAATTGTTC | 286053 |
rs570656007 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346734 | TTTGAAGTGGATATT[A/G]TATGACCAAATCTTA | 286053 |
rs570656453 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211373 | TAGCATATTGGATAC[G/T]CTGTTCTACTTTGCT | 286053 |
rs570659758 | in-del | -/ACAG | 0.0236746 | 0.106192 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218292 | GATTCTGACATACAA[-/ACAG]ACAGGTAGGTTTAAT | 286053 |
rs570692246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353513 | GAAGCATGAAAACCC[A/G]TCATAGCCATGAGCA | 286053 |
rs570693030 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204886 | GATCCGGCCAGTTTC[C/T]ACCAGAATGATCATT | 286053 |
rs570717359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317091 | CACTCCTGGCCTATT[A/G]TTTCTGATTTCACAT | 286053 |
rs570722441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243583 | AAAATCAAGAATCAT[A/G]TCTCAATGTTATTAA | 286053 |
rs570723338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213470 | ATTAAATGGTAGTCT[A/G]CCTAAGGCACCCATG | 286053 |
rs570723903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288857 | TGGAGTGCAGTGGCT[C/T]GATCTTGGCTCACTG | 286053 |
rs570725635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220413 | AATTTTAATGGTTTG[C/T]ATAGAAAGAGTTTTC | 286053 |
rs570726650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250925 | TTAGTATTAACCTAC[A/T]TTCACTAAATCTTTA | 286053 |
rs570729044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151062 | AAAAGATGTAATAGC[G/T]CTACAAAATTATTTA | 286053 |
rs570760054 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207308 | AAGCAGGAAACACAC[-/T]TGTGTAGTTTAAAAA | 286053 |
rs570765724 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347401 | ACCTTGACTCTTCCC[C/G]TACCTCCAGAGATAC | 286053 |
rs570768969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105148 | TGTCCCACAGCTATT[A/G]TTTCATATATTTTGT | 286053 |
rs570789670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281854 | CAAAGTGCTGGATCA[C/T]AGGCATGAGCAACCA | 286053 |
rs570814007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258742 | GAGAGAGGTGGGGGG[G/T]TTATGGGAGTGGCAA | 286053 |
rs570824115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201140 | AGCTTGGAGAAGTTT[A/G]TTATTACTGACCTTC | 286053 |
rs570831165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333789 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCGC | 286053 |
rs570840758 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304382 | TTAGCAGAGGAGTGA[C/T]GTGATCCATGTAGGT | 286053 |
rs570857031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194354 | ATTGTACAGTGTGTA[C/G]CCTTTTGAGTGGCTT | 286053 |
rs570861772 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282692 | AGGACAGTTACTCCC[C/T]GTTGTCTGTGTATAA | 286053 |
rs570862900 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091568 | CCCAGCGGGGAGGGG[A/G]AGGGGGCCATGCAAA | 286053 |
rs570864292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158519 | ACCACAGCACTCCAG[A/G]TAGGTACTGAGGCGC | 286053 |
rs570868151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341480 | AGGCTTTGAAAATGC[A/G]AAGCAAGATCAACCA | 286053 |
rs570870272 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109395 | TGACCGGTGGGTGTG[C/T]TGGACAACAGAGAAT | 286053 |
rs570873392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296978 | TAGAAAATATAGAGT[A/G]TACTTAGAAATTCAG | 286053 |
rs570884813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233958 | GAGGCAGGCGGATCA[C/T]GAAGTCAGGAGATCG | 286053 |
rs570886309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265982 | GAATTGTCTCTCAAG[A/G]GCACACTTCAAAATA | 286053 |
rs570890917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200618 | AACATTTTTTCCTCC[A/G]TTTCAACCTTGGTTA | 286053 |
rs570892035 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167567 | TTGAACCCAGGAGGC[A/G]TAGGTTGCAGTGAGC | 286053 |
rs570926831 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310784 | TTTTCCTCCATGCTC[A/G]TTTACCGAGGAGTAT | 286053 |
rs570949224 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272204 | TATTTTTAGTAGAGA[C/T]GGGGTTTCATTGTGT | 286053 |
rs570953777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160443 | TGAAGGAAGGGCCTC[C/T]TTCCTCGGAAGGGGT | 286053 |
rs570960832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207248 | AATTGGTATTTAAAG[C/G]AATAAAGAGTAAAGG | 286053 |
rs570999776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263865 | TAAAGAGAGATTTTT[G/T]TGTTTTACTCACTGC | 286053 |
rs571011046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179274 | CCAAGGAAGTTAAAG[A/G]CTACAGTAAACTGTG | 286053 |
rs571034072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121801 | GGTAGGTAGGTATCA[C/T]TACCATTATACATAT | 286053 |
rs571035791 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344751 | CATCTCAAAAAAAAA[-/G]AAAAGAAAAGAAAAT | 286053 |
rs571038143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229243 | AAGAGAGATGCAAGA[A/G]ACTGGGAGAAATAAT | 286053 |
rs571039204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125127868 | TTATGTTTCATATAC[A/G]CATAGCCTGAAGGTA | 286053 |
rs571056835 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200430 | TTTCTCCTTCACTTA[C/T]GAAGCTTAGTTTGGC | 286053 |
rs571065935 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137465 | TATGCTAATCTAAGG[C/T]AGTTGCTATCCACAT | 286053 |
rs571071544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360773 | GAGTATTTCTGGGTT[C/T]GCTTTGTTTAGAAAT | 286053 |
rs571094557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270558 | AATAGAAGCAAGTTA[C/T]GATCAGCAGTGTGTT | 286053 |
rs571102236 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316022 | GTGTTGCCCGGGCTG[A/G]TCTCAAATTCCTGGG | 286053 |
rs571116321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356238 | TGTCTGTGTGTATGG[C/G]GGGGGGTGTTCTGGA | 286053 |
rs571122697 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168680 | CCCTCGTGCTCTAAT[C/T]TCTTCCCAGAGGCCT | 286053 |
rs571129643 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091045 | GCAATCAGGAGACCC[A/G]GTTTTATGGCTCTGT | 286053 |
rs571133130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138078 | ACTTTCTTTTTACCT[C/T]CTGAATGAAATAAAA | 286053 |
rs571136567 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101329 | GAGATACTACACAGT[A/T]CCCCACTTAGGAAGG | 286053 |
rs571144191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272758 | ATATATACACACGTA[C/T]ATATATATACACACA | 286053 |
rs571158645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312030 | CAGAGATCAGGTCAT[A/T]ATTGCACTCCAGCCT | 286053 |
rs571166486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208232 | ATTCATCTGTTTGAT[G/T]AAAGACATGTTTGTT | 286053 |
rs571168995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128867 | CACCCAGATAAGCCT[A/G]GATTCTCTCCCCACT | 286053 |
rs571181515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364038 | AACCCCCACCTCCTG[A/G]ATTCAAGTGATTTTC | 286053 |
rs571194176 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284830 | TCAAAACAGTGAAAA[C/T]CCTGTCCCCTTTTCT | 286053 |
rs571202523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144357 | TGATTGGTCTGTTAG[C/G]CATGCCCACCTGGAT | 286053 |
rs571206907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252858 | AGTTAAGAGCGCAAG[C/T]TCCGGAAAGAGCCAA | 286053 |
rs571220303 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271786 | TTTTAATGACTCTGT[A/G]ATCATGTGTATGTTT | 286053 |
rs571237203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122842 | ACCAGTTAATAATAT[A/C]CTGTTTCCCAGCCAA | 286053 |
rs571247773 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118808 | GCTGCTCTCCTTTTC[A/G]GTTGTGTGGGTTAAT | 286053 |
rs571269107 | in-del | -/CTC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221467 | CAGGCTGGTCTTGAA[-/CTC]CTGGGCTCAAGCAGT | 286053 |
rs571269786 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259705 | TTTAACAGTAGTAAT[A/C]ATAATATAAACAATA | 286053 |
rs571278658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222916 | AAAGGAAAAGAAATA[A/G]CCAGGTGTGGTGGTG | 286053 |
rs571296125 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334297 | GCATGCGTTAAGTAC[G/T]ATCTGTAGCACAGCG | 286053 |
rs571301081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305702 | TAGAAACTCGTATAC[C/T]TGCATACTCAGTTTA | 286053 |
rs571302868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130791 | CTAATCTAGTGCTGC[A/G]TGGTTAAATTCTTTT | 286053 |
rs571335107 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286609 | TGAGCCACTGCGCCC[A/G]GCCCAAATAACATCT | 286053 |
rs571336898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174156 | ATTTCCTTCCCAACA[A/C]TTTTTATAGTTTGCA | 286053 |
rs571344390 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337906 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAACAA | 286053 |
rs571365251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189593 | AGATAAGCTGCCTAG[A/G]AAAAGAGGGTCAGAA | 286053 |
rs571371984 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194192 | CACAATCAGTTGTCC[C/T]GCACAGTTCTATCAA | 286053 |
rs571382853 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231576 | TGCACACTATAGATT[A/G]CAACCCACAGTATTT | 286053 |
rs571387362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349929 | TGGCTAAAACCTATA[A/G]AATCATCATTGTGTG | 286053 |
rs571406865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312736 | CAGGGCAAAAGGCAA[A/G]AGATCTGTTTCAAGT | 286053 |
rs571434814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321340 | TTTGTATCATATGTA[A/G]AAGTAAAATGTGTAA | 286053 |
rs571478014 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123447 | GTTATTTTTCTCTCT[G/T]AACAATCCTATGAAA | 286053 |
rs571496485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231705 | AGTTGTATATACTGG[G/T]TTATGATAAAAATAT | 286053 |
rs571500845 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178824 | GCAGTGAGCCGAGAT[C/T]GTGCCACTACAGCCT | 286053 |
rs571506056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196526 | GTCCCTGCAGAGGAC[A/G]TGAACTCATCCCTTT | 286053 |
rs571523325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093955 | GTGCAAGCCACTATG[C/T]CTGTGTAAGTTTAAA | 286053 |
rs571529410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278534 | TTGCCCTTCACACTC[A/G]GGGTGACTCAAAGTG | 286053 |
rs571539030 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256653 | GAGGACTGTTGGGTG[C/T]GGTGGCTCACGCCTG | 286053 |
rs571554419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232688 | TGGGCAACTCATAGC[A/C]AATTTTGTTTCATTT | 286053 |
rs571555705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239115 | TTTTCATCCCATTTG[A/G]CAAGGTTGGTTTCAT | 286053 |
rs571563723 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327340 | AATTACTGAATGAAT[C/G]TAGTATAATTACCAA | 286053 |
rs571575613 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252520 | GACAGAGCGAGACTC[G/T]GTCTCAAAAAAAAGA | 286053 |
rs571576128 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254629 | TTTTAATAAAGGACT[A/G]TAATTTGATTGGCTT | 286053 |
rs571577491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279390 | TTCTTATTTAAGAAT[C/G]ATAATGATAATGACC | 286053 |
rs571593253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318426 | AAGTAAAATAATGTT[C/T]ACCTATCAAATTGGA | 286053 |
rs571600139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183217 | GAAATAGGCTTTCTT[G/T]TAAATATAAGCATTT | 286053 |
rs571611212 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197112 | GCCCTTTATCAGATA[A/G]GTAGATTGCAAAAAT | 286053 |
rs571616059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160956 | GCCTCTGATGTATCA[C/T]ATGCAGGTTGTCAGC | 286053 |
rs571635488 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276975 | GTGTGGTTGGTGGCC[G/T]TGGTAATAACTTGTT | 286053 |
rs571658905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176242 | CCTTTGCGCATATGT[A/C]TGCTCTTGCTAGAGT | 286053 |
rs571673907 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240966 | AAAATTAGCAGCTTC[C/G]ATGGTCACTGGTGGT | 286053 |
rs571692419 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132366 | GTTGGGATTACAGGC[A/C]TGAGCCTCTGTGCCT | 286053 |
rs571699886 | in-del | -/AATA | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093535 | CTCTACTAAAAATAC[-/AATA]AATAAATAAATAAAT | 286053 |
rs571704307 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241236 | TTTGGAAATACATTT[A/C]TTCATCAGATACTCA | 286053 |
rs571723324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132818 | TAAATTGTTAAAAAT[A/G]GATACAATACTTAAG | 286053 |
rs571763671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138824 | GAGACTTGAGACTTT[C/T]TGTTTGACCCAGGAG | 286053 |
rs571784470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365127 | AGTCCCAGTGGCCCA[C/T]TCAGTCTCTCTTCTA | 286053 |
rs571791232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103040 | TGGGAGGCCGAGGCC[A/G]GCAGATCACGAGGTC | 286053 |
rs571822060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328719 | TCATCGGTGTTTCAT[C/G]AGAAACAGTAGCAAC | 286053 |
rs571839775 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301546 | CTTGTTAGTTGTTAG[C/G]AGACAGCGTCCCAGT | 286053 |
rs571854284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152823 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 286053 |
rs571882387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336268 | TTAAATAATCAATTA[C/T]TCAATTAAATTCAAT | 286053 |
rs571882494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208952 | TTCCTCTCCAATGGT[A/G]CCAAGGCTTAATTTT | 286053 |
rs571889069 | snp | C/G/T | 9.96983e-05 | 0.00705976 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102285 | TATTATTCTGACTTA[C/G/T]GAATCTTGTTTCATT | 286053 |
rs571900375 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343812 | CATCCTGGCTAATTC[A/G]GTGAAACCCCGTCTC | 286053 |
rs571924767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103354 | CTTTGGAGTAGAATC[A/G]TTTTTATTTTATTTT | 286053 |
rs571932829 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247832 | GAAAGCCATTTTCAG[C/T]CATTATTACTAAGAC | 286053 |
rs571942603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116837 | TATGGGCCAATGGCC[A/G]TACTGAAGATATATC | 286053 |
rs571945758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202182 | TTCCTTCGTGAGGCA[A/G]TGCCCCGCCCTACTT | 286053 |
rs571969849 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248023 | AAATCTGTAGAGAAA[A/G]GTTGGCTCATTCAAT | 286053 |
rs571981704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343955 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 286053 |
rs571982776 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329913 | AGGTGGTGGTGGTGA[A/T]ACCATGTAGTAAGAC | 286053 |
rs571996304 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109978 | TTTATTATGTACTTT[G/T]CTGCCATCTTACACA | 286053 |
rs571997284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322623 | GTTCAAACAAGTACA[A/G]TAAGGTAAGAAAAAG | 286053 |
rs571997784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247262 | TACCTGAGCCCAGGA[C/G]GTCAAGGCTGCAGTG | 286053 |
rs572004058 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110562 | CATGAGAAAAATTGA[A/G]GCTTAGTGAAGTTAC | 286053 |
rs572013274 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234187 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 286053 |
rs572015568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197559 | TCCATTGGTCTGTAT[A/G]TCTGTTTTGGTACCA | 286053 |
rs572038351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146963 | TTTGATGTAAGTTTG[A/T]TGTGCTGGCACATAA | 286053 |
rs572048098 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239334 | AAAAATTGGGTGGGG[C/T]ACTGTGGATCACTCC | 286053 |
rs572067202 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253467 | GATGCAGAGTTTCGG[A/G]TGGAGTTTTGTTTTT | 286053 |
rs572076083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156453 | TTATATTGGATTACA[G/T]CTACATATTTGTTTT | 286053 |
rs572084957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096492 | GATCCATACTTGCCT[C/T]GATTGCCATGGAAAG | 286053 |
rs572086070 | in-del | -/AAT | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280371 | TTTCTAAACTAATGA[-/AAT]GTCCTTTCTAAAACA | 286053 |
rs572088605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286950 | CTTCAGTAGACGCCA[A/G]TTGGGAGGTGAACTC | 286053 |
rs572097790 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273422 | GTAACTATGGTAACA[A/G]TTATTTGATCTCACA | 286053 |
rs572111828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294240 | TCTTTCTGTCTTTTG[G/T]CTATTATGGATAGTG | 286053 |
rs572137984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351541 | AGTTGGACAGCCGGC[A/G]TATGCTTCTAACAAC | 286053 |
rs572145165 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314050 | TTTTTCAAAGACCGG[C/T]AATCAAATAGGATAG | 286053 |
rs572176905 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154505 | CTATTTTAGTGCTCT[A/G]AAAGTTAAAAAAAAA | 286053 |
rs572177525 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319181 | ATTAAACACCACTCT[C/G]GTCATCCTGAGCACA | 286053 |
rs572186392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137095 | CAAAATTTTTTTTTT[A/G]CTTTCCAACAATAAT | 286053 |
rs572190574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253978 | CCTAGTGTTCAGGAT[A/G]CTTCTCAAAAGGCCT | 286053 |
rs572208495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190900 | TTTGAGATGGAGTTT[C/T]GCTCTTATTGCCCAG | 286053 |
rs572213182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196786 | TGCCCAACTGTCTTC[C/T]ACAGTGGTTGAACTA | 286053 |
rs572233763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146637 | CATTCTCAGCAAACT[A/G]TCGCAAGGACAGAAA | 286053 |
rs572270641 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180487 | ATTAAGCAAAAGAAG[A/G]TTATGTCTTTTCTCT | 286053 |
rs572276988 | in-del | -/CAGT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115130 | GCTTTTTGAGTGAAC[-/CAGT]CAGTCAACCAAGTAA | 286053 |
rs572278078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268410 | GGATCCCAAGGTTTT[A/G]TCATGGGCTGCCTAG | 286053 |
rs572287491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300391 | TGGTCTCGAACTCCT[A/G]AACTCAAGTGATCCT | 286053 |
rs572311706 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212846 | TAATCACCGAGGCAT[A/G]TACCTGGTATGCCTG | 286053 |
rs572339227 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267717 | AGGAGGTTGAGGCTG[A/C]AGTGAGCCAAGATCG | 286053 |
rs572347478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365608 | TGCCTGTAATCCCAG[C/G]ACTTTGGGAGGCCGA | 286053 |
rs572348489 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297978 | AAATAATGCTGACTG[A/G]GCCAGGCACAGTGGT | 286053 |
rs572349555 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202316 | CACGCTGGGAGCTGC[A/G]GACCGGAGCTGTTCC | 286053 |
rs572350806 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286400 | TCACTGCAACCTCCG[A/C]CTCCTGGGTTCAAGT | 286053 |
rs572351024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163119 | CACTTGTAATCCCAA[C/G]ACTTTGGGAGGCCGA | 286053 |
rs572352458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293470 | ATTTTTATTTACTGA[C/T]TCCAGTGGGTTAATT | 286053 |
rs572358315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198649 | TTGGTCTAAAATTCT[C/G]TTTTTTTGTTGTGTC | 286053 |
rs572375323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161483 | ATATTCAGAAAGATC[A/G]AGTCAGTATTACTTA | 286053 |
rs572391956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248945 | GAGGCTGAGGCAGGC[A/G]GATTACTTGTGGTCA | 286053 |
rs572402447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133759 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAACAAAA | 286053 |
rs572410745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296519 | CCTGCCTCAGCCTCC[C/T]TAGTAGCTGGGATTA | 286053 |
rs572459755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346325 | AAATGAAGAGGAGGA[A/G]ACAGACTCAAGATAA | 286053 |
rs572475594 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289369 | ATTGCTAAGTGCCCC[G/T]CTCTCAGCCAATCTG | 286053 |
rs572485272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203939 | TAGATATATTAGTCA[A/G]TTTACTTTCCTATGG | 286053 |
rs572486171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105226 | TTCATTTACGGCTAA[C/T]AGCAGGTGTCACTCA | 286053 |
rs572507609 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126040 | GGAGGCACAACCTCA[A/G]TCTTCCAGGGTTTTG | 286053 |
rs572508984 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204145 | CTTAGTTCATGTGAC[C/G]TTTTTTCCCCCATGG | 286053 |
rs572517071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316880 | ACCTCTCAGACTCAA[A/G]GAATTCTTGCACCTC | 286053 |
rs572527664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232646 | GCCCAGTAGAATGTT[C/T]TGCGTACTCATCCCC | 286053 |
rs572529152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243204 | ATACATTCAATAATA[A/G]TGGACGTATATATAC | 286053 |
rs572530228 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170158 | TGTCTTCTCTTCATT[G/T]TCACTTTATTTCATT | 286053 |
rs572535150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338935 | AAACTAAATTCACGC[G/T]CTGCCCTAGATTTAC | 286053 |
rs572542675 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177737 | TTCCCCAAAGGACAA[A/G]CACTTCTCTAATGGA | 286053 |
rs572547621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198354 | CTTATTATTTTGAGA[C/T]ATGTTGCATCGATAC | 286053 |
rs572554359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211942 | TTCTAGTTTCTGATA[C/T]TCTGTTCCATTGGCA | 286053 |
rs572575169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118769 | TCAACTCTTCCAGGA[A/G]TGAGGACTATACCTC | 286053 |
rs572575763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338351 | ATATAGTGAGATGAA[C/T]AGAATGCAAAAGTTT | 286053 |
rs572580871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274613 | ATCTTCAGTTTCACT[A/G]ACAAGGAATAGAATT | 286053 |
rs572588631 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229175 | CACAACAGAAGTCCA[A/G]GCAAGACATGGAGAA | 286053 |
rs572621320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112285 | AAGGGAAACCCTTGT[A/G]TATTGTTGGTGCGAA | 286053 |
rs572622937 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243061 | AAAAAATCACCAGAC[A/G]TGGAAATGTCTGTGC | 286053 |
rs572637119 | in-del | -/GA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240175 | CTGTCTCCCAGGCTG[-/GA]GTGCAGTGGCAGATC | 286053 |
rs572660288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176594 | TAGACCTGTGTATTC[A/C]GCAACACTGGAGATA | 286053 |
rs572670053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177173 | AATAAAAGTTTTTGA[A/T]CATTTACTATGGGCC | 286053 |
rs572676640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125159 | CTTTCCAATCTGGAT[A/G]CCCTTTATTTCTTTT | 286053 |
rs572696572 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263760 | ATCTCAAAAAAAAAC[-/A]AAAAAAAAAAGAAGA | 286053 |
rs572697361 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266573 | TATACAATGTATTAT[C/T]AATTTGTCCTGCTAT | 286053 |
rs572697946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211130 | TTATACATTTTATAT[A/G]TGTATGTATAATAAC | 286053 |
rs572700941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186030 | TAGGCCTGGGGTCAG[C/T]AAACTCTGGGCCATG | 286053 |
rs572711106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352333 | AAATACAAAATTAGC[C/T]GAGGTGGTGGTGCAT | 286053 |
rs572721085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169387 | AACTTAATGATAGAT[G/T]TGACATTCTCTACTT | 286053 |
rs572722887 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184806 | GGCTCCCACAGTATT[C/T]GTGTAGCCAGGTCAA | 286053 |
rs572725380 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307817 | GAGTTAAAAACGATT[A/G]CTGTGGTCTCAGAGG | 286053 |
rs572726730 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151979 | TGTATTTCTGGTTTC[A/G]TTATTTGCCTTTTCT | 286053 |
rs572737444 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118091 | GAGAAGGGTCACAAC[A/T]GTAATCTTAGCACTT | 286053 |
rs572753746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353861 | GCACTCCAGCCTGGG[C/T]GACAAGGGCAAGACT | 286053 |
rs572760744 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341232 | ACCTACTGCAAGACC[C/T]AGATGTCATTCACAT | 286053 |
rs572763837 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111849 | ATTGGATATGTCAAT[A/G]CAACTGACCTGATAT | 286053 |
rs572777051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316596 | TCTTTTCTTTTCTTT[A/C]TTTCCTTCTTTCCTT | 286053 |
rs572782594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172302 | GGGAAAGCTGAGAGA[A/T]TTTCTGGTTCTTACT | 286053 |
rs572783909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270195 | GAAAGGTCCAGGTGC[A/G]GTGACTCATGCCTGT | 286053 |
rs572798384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121294 | ATTTTACTCCAAGAC[A/G]AAGATTTGCGCTTCC | 286053 |
rs572813061 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178761 | TGTAGTCCCAGCTAC[A/T]TGGGAGGCTGAGGCA | 286053 |
rs572819746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217753 | CTGTTATTACAGCTG[G/T]GCTGAGGTACTTAGT | 286053 |
rs572843246 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165536 | GTTTAATGATATTAT[C/T]TTACAGTGCAACATG | 286053 |
rs572848301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263602 | TAAAATACAAAAAAT[A/T]AGCTGGGCATGGTAG | 286053 |
rs572863486 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136391 | CTGACTTTAGCAGGC[A/G]GAATAGATAGACATT | 286053 |
rs572870259 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354441 | GGATCAACAATTAAT[A/G]AAGTTAACTTCACAT | 286053 |
rs572874223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171793 | TGAGTGCTTACCAAG[C/T]ACTAGAGAGTATTCT | 286053 |
rs572893684 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132288 | AAAATGTTTTGTACA[C/G]ACAGGGTCTCACTAT | 286053 |
rs572893800 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096124 | TCTATCATCAGCATA[C/T]AGCTTTACTAAGGTC | 286053 |
rs572900629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257404 | CTCAGAAACCAAAGT[C/T]AGAGAGTTGAAAAAG | 286053 |
rs572900944 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285574 | TGTTTTACTTTAAAC[A/G]TGTACATTTAGGTAA | 286053 |
rs572914295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125129781 | TTGCAATCTCTCTCT[A/G]TCCTTTTTATTTTTT | 286053 |
rs572915631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157585 | AACATTTTGCCTAAT[A/G]AACAGAGACAGAGAC | 286053 |
rs572928084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331801 | AGCGTATAGCATGGT[C/G]CACTTCTTGCAATCA | 286053 |
rs572941272 | snp | A/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258781 | GCTTCTTATTTAGTC[A/G/T]CCAGAGGTTAGTTGA | 286053 |
rs572947344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142360 | AAAGCCTAGATTTGA[A/G]TGAAGTCTAATTCCA | 286053 |
rs572948667 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343225 | AATCTGAGGACAGCG[C/G]TGAGCACTAACAGAT | 286053 |
rs572952885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100835 | CAAAGTGCTGGGATT[A/T]CAGGTGTGAGCCATT | 286053 |
rs572981601 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156278 | AATTTTCAAAAAGAT[-/A]AAAAAAAAAGAATTT | 286053 |
rs572995859 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297071 | TTACAATCACTTCAC[C/T]GGGCCATTTTACTGT | 286053 |
rs573004227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098468 | ATGATCTTACGTACA[C/T]TTTCAAAGGTTTACT | 286053 |
rs573012023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281912 | TCTTAGAAGGCTCCA[A/G]TATACTTCCTAATCT | 286053 |
rs573029326 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134502 | AGTGGTTTTAATTTG[A/T]TTTTTCTAATGATCA | 286053 |
rs573032598 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101779 | ATTCTGCTTTCACTG[A/T]CTCTGGGATCTCACC | 286053 |
rs573045248 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276104 | GAGATTCTTCCAGAA[G/T]TGGCTTTTTACAAAG | 286053 |
rs573047253 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141462 | CCATCATTTATTAAC[C/T]ATGTCATCTGGGGCA | 286053 |
rs573071195 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312029 | GCAGAGATCAGGTCA[C/T]TATTGCACTCCAGCC | 286053 |
rs573088942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099894 | ATGGGAGAAGTAATG[A/G]TGTATTTGTTTGCTG | 286053 |
rs573090287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324437 | ATAAATGAATAGACA[C/T]TGTATGTCATATCCA | 286053 |
rs573090789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135114 | GTAGAGATGGGGTTT[C/T]ACTATGTTGTCCAGG | 286053 |
rs573093212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340208 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 286053 |
rs573095929 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091520 | CCATCCAGGCTGCAC[A/C/G]CGACTCTGCAGACCT | 286053 |
rs573110614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277583 | GCGATCTCAGCTCAC[A/T]GCAAGCTCCGCCTCC | 286053 |
rs573125705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227326 | CCATCAGTCCTTCAG[A/T]TAGCAGTGAGAAGAT | 286053 |
rs573146424 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136813 | TGGAAAAACAATCTT[A/G]GAAGTCACTGATGAT | 286053 |
rs573153252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326281 | TAAAATAAATAATAA[A/G]AATAAAAATCAAGTC | 286053 |
rs573174321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137598 | TACTGGTGTGGTTTC[C/T]CTGGCACAGTAGGCA | 286053 |
rs573202398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341052 | AGAGAGAGGCTTTCC[C/T]AATCACTTTAACCAG | 286053 |
rs573208314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236127 | TGAAGGCAAGTGAAA[A/C]TTCAGAAAGAAGTGG | 286053 |
rs573225323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142331 | AAAACTACATAGCTA[A/G]CATGTAATTTCATAA | 286053 |
rs573226770 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106812 | ACCAGCCTGGCTAAC[A/G]TGACGAAAACCTGTC | 286053 |
rs573231239 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128145 | TGGTAGTAGGCTCTT[A/G]TAAGTCAAATTAAGA | 286053 |
rs573260835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318550 | TAGACCCAAAAGTAT[A/G]TATACAGTGATGTTA | 286053 |
rs573267615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152972 | TGAGGCAGGAGAACC[A/G]CTTGGACCCAGGAGG | 286053 |
rs573269602 | snp | A/C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334994 | CTCCTGGCCTCAAGC[A/C/T]GTCCTCCCACCTCAG | 286053 |
rs573273301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180250 | AAATTGAGCTTTATT[C/T]GTTCTTTAGCCATAC | 286053 |
rs573287304 | in-del | -/A | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367547 | AAAAAAAAAAAAAAA[-/A]GAATGTCTTTCAAGT | 286053 |
rs573292346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317598 | TGTCTTCCATGTTTT[A/G]TTAATCAAAGACAGT | 286053 |
rs573346009 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259819 | GGTCAGAAAGCCTGA[A/G]TCTCAGAGGGTAAGG | 286053 |
rs573349494 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311100 | ACTGTGTTTGTGTAA[C/T]CTGGGGAAAGATTTT | 286053 |
rs573359542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194022 | GTTGAAAGAGGAGGA[A/G]GAATGCTTGCAAAAT | 286053 |
rs573373152 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348375 | CATCCTGTGAGGTTG[C/T]AACATCTAGGGAATC | 286053 |
rs573379554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296474 | ATCTCAGCTCACTGC[A/G]ACCTCCAACTCCCAG | 286053 |
rs573397511 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283296 | GCTCATGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 286053 |
rs573398559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285879 | AGCTTGGTGAGGTTG[A/C]GTTGTCCAAGGTCAC | 286053 |
rs573402613 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152083 | TTTTAAATCATGTTT[A/C]ATACCTAAGCCAATG | 286053 |
rs573404566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160463 | TCGGAAGGGGTTGGG[A/G]GTGGCTTGGGGTATG | 286053 |
rs573432956 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281160 | AAAACACATGAGAAA[G/T]TTATAGCTAGCTCTT | 286053 |
rs573433819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289684 | CTTTAAAAGTAGCAG[A/T]TGTTTGTGGGTGTGC | 286053 |
rs573440488 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245034 | ACACCTGTAATCCCA[A/G]CACTTCAGGAGGCCA | 286053 |
rs573448896 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162092 | ACTAAATAGGAACTT[G/T]AAGTGGAATAAATTC | 286053 |
rs573470348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265382 | ATGCACCACTGTGCC[C/T]GGCTGATTTTATATT | 286053 |
rs573489583 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165652 | TCTCTAATCACTGAG[A/C]ATCAAAATTATATAC | 286053 |
rs573505384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251791 | TTAAAGCAAAGTTAA[A/G]TCATTTGCTCAAGGT | 286053 |
rs573523625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257730 | TAGTAGAAACGGGGT[C/T]TCATTGTGTTAGCCA | 286053 |
rs573533067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264642 | TCAAACTCCTGACCT[C/T]AGGTGATCAGGGTGG | 286053 |
rs573538734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291655 | CAGTGATCTTAGTGA[C/T]GGTAAAGATAGAGGA | 286053 |
rs573541000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362639 | AGGCACAGAGAATTT[A/G]GTCACTTACCCAGAG | 286053 |
rs573541318 | in-del | -/GAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175735 | TAATTGGAAGAGGAG[-/GAG]ACTTTGACTTTGCCC | 286053 |
rs573552276 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311671 | TCAGGGATTTCCCCT[G/T]AACTATTTTGGAAGA | 286053 |
rs573556690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290075 | ACTAGTGAGGAAAAT[A/G]GGGAACTTCTAGACA | 286053 |
rs573564285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252885 | CCAAGGTTATTTAAA[A/G]TGTCCTCACCTACCA | 286053 |
rs573567722 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275554 | CATTTGTATTTCCTC[A/G]TTGGCTGCCCAGCCC | 286053 |
rs573580938 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158143 | GAAGGAGGCTGTGAG[A/T]TAGGTCCAGCACTTT | 286053 |
rs573586611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125195913 | TTTTTTTGAGATGGA[G/T]TCTCATTCTGTCACC | 286053 |
rs573587196 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306373 | TTAAAAAAAAAAAAC[C/T]GAGCAACAGCTGTTT | 286053 |
rs573601844 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252467 | GGAGGCGGAGCTCGC[A/G]GTGAGCTGAGATCCC | 286053 |
rs573604609 | snp | C/T | 0.040671 | 0.13668 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298712 | GTTTTTTTTTTTTTT[C/T]CCCCAGTTTAGGTCT | 286053 |
rs573606787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145448 | TTTCTTAATTGACGT[A/G]TCAGGTGACAGGTCT | 286053 |
rs573607582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258972 | CAATGGCACGATCTC[A/G]GCTCACTGCAACCTC | 286053 |
rs573610928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350231 | GTGGAGAACAAGAGT[A/G]ATGTGATAGAGAAAG | 286053 |
rs573612145 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247340 | ATTGTCTCCAAAAAA[A/T]AAAGTTAAGGACACT | 286053 |
rs573618194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116279 | TGGCAGAACATTTGA[A/C]CTTGGCAAGGCAGTA | 286053 |
rs573628860 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301471 | CACTACATGGAGGTG[A/G]CGGTGGGGTGGTGGT | 286053 |
rs573636165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123032 | ATGTCTTTAAAGGCT[A/C]AGAATGGGTTAAAAT | 286053 |
rs573645423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108428 | GATACTAAGGCAGCC[A/G]GTATCAGCACTTAAG | 286053 |
rs573651061 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209352 | TACAAGTATATCTGG[C/T]TTTATTTAGGGACTA | 286053 |
rs573653304 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364623 | TTAATGCATGAATGG[A/G]TGCATGCCTGTGTGG | 286053 |
rs573653916 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191917 | ATTTACCCAGTGTCT[-/CA]CAGTCAAGAGGCCAC | 286053 |
rs573672556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342701 | CAGTCAGCAGGTTTT[C/T]GTGGGGTATGTTTTC | 286053 |
rs573681217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109270 | CTATTTATAAAAGGC[A/G]TTATTGTGGGGATTA | 286053 |
rs573686062 | in-del | -/ACTTTGGAATCATCTGTGGTATTATTCTTCAGAGTAGA | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149377 | TTACATTATTTCATT[lengthTooLong]AAAGAAAAACTGACA | 286053 |
rs573695556 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192864 | GATAGATGATGATGA[C/T]GCGCTCTACTGCTAA | 286053 |
rs573706052 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306394 | ACAGCTGTTTTCACC[A/T]CTCATTGTCCCATCT | 286053 |
rs573707417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341857 | CAAGGACCCTTTAGG[A/G]TCGAGAGTCCATGTG | 286053 |
rs573716513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245972 | GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 286053 |
rs573735260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214926 | ATCACCATTAGCCAC[C/G]TCCAGAACTTTTTCA | 286053 |
rs573741399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239531 | TGAGAATTGCTTTAA[C/T]CCGGGAGGCAGAGGT | 286053 |
rs573745640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335571 | TTTCCATTATTGTCT[A/T]TAAACAAACAAAGGA | 286053 |
rs573749137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175417 | ATACTTAGAGTACTA[G/T]TACTAAGCAGAACAC | 286053 |
rs573760913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201584 | TCCCAGAGGGGCACC[C/T]GCCTGTATGAGTTGT | 286053 |
rs573766190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167118 | ACTTCTTTCACTTTC[A/G]CTGTGCCTTTAGTAG | 286053 |
rs573770904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215674 | TGGTTTTAGGTCTAA[C/T]GTTTAAGTCTTTAAT | 286053 |
rs573783861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334832 | CTGTCACCCAGGCTG[C/G]AGTGCAGTGACCTCC | 286053 |
rs573788506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222444 | ATTTTCGTGCTGTGC[A/G]ATAGATCACTAAAAC | 286053 |
rs573828807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101756 | CCAGAAGACAAGTTT[A/G]TACAGAAATTCTGCT | 286053 |
rs573829943 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122297 | TAAGTCTTGATTACC[A/G]TGAATTGACTTCTTG | 286053 |
rs573839183 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225499 | GAGGTTGAAGAAGTG[A/G]AAATCATCAGCTCAC | 286053 |
rs573844810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307008 | TGCTACTACTGAATT[A/G]TGCCAGTGGATAAAA | 286053 |
rs573853873 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303478 | AAATAAAAGGTCAGG[C/G]GTATCCATTTTTTCC | 286053 |
rs573865376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279520 | GGGGTAAGTAAGGTC[A/G]AGTCTGCTTAACTTT | 286053 |
rs573871830 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120082 | CATATAATCAATATG[A/G]AAGTTACTAATATTA | 286053 |
rs573876663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166328 | CTGGAGTGCAGTGGC[A/G]CGATCTCAGCTTACT | 286053 |
rs573883758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174639 | TATTCAAACTAGACA[A/G]ATAACATTCTTACCC | 286053 |
rs573897039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207720 | GGGTGAGTCTTCTGC[C/T]GGTTAGGAGGGGCTT | 286053 |
rs573902894 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222598 | TGTTTTAGATTCCAC[A/G]TGTAAGTGAGATCAT | 286053 |
rs573919738 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213322 | GTCACATTATTAATT[A/G]CATTCTCTCTTGGCC | 286053 |
rs573920458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267380 | TGTGTAAAGGCTTTC[A/G]TTTGTATGTATTTTT | 286053 |
rs573933427 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162516 | GTGCCTGCCCACTGA[A/G]TAGCTGTGTGGCCAT | 286053 |
rs573941055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181003 | TGGTGGTAGAAGTCC[A/G]TCTAAAGTGTATGGG | 286053 |
rs573952926 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352307 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 286053 |
rs573956557 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185730 | ATATGAAAAATAAGC[C/T]TATTACATGTTAATA | 286053 |
rs573960471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313736 | CTTCCGTGGACAAAG[C/T]GTGACACTGTTCAGT | 286053 |
rs573965813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161569 | TTGGGAGGCTGAGGC[A/G]GTTGGATCATCTGAG | 286053 |
rs573982247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110917 | TTCAGGGCCTTTGTA[C/T]TGACCCTAGACTGTC | 286053 |
rs573988395 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162344 | TAGGTGAAACTGAAC[A/T]TGTTATACTACATGT | 286053 |
rs573988541 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137790 | ACTATATGACTTTAG[G/T]TCAAGGTACTTAACC | 286053 |
rs573999130 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213112 | AAAAAGAAATTAAGT[A/G]TTTGGCTTTGAAAGA | 286053 |
rs574018887 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149300 | ATAGTCTATGAAATA[A/T]ACTTATAAGTAACTA | 286053 |
rs574021678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267027 | TTTTTTTTTTTGAGA[C/T]AGAGTCTTGCTCTGT | 286053 |
rs574022165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181833 | TCCCTGGCAGTTATC[A/G]GAAGACAACAAGTTA | 286053 |
rs574045305 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256723 | GAGGTCAGGAGATCG[A/G]GACCATCCTGGCTAA | 286053 |
rs574049895 | in-del | -/ACA | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211689 | GGATTTTATTAATCT[-/ACA]ACAACCCCATCAACA | 286053 |
rs574056222 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156957 | GAAGTTACCATTTTA[A/G]TTAAACCAAATTTGG | 286053 |
rs574062686 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271239 | GCACTGCAGACTGGG[A/C]GACCAAGTGAGACTC | 286053 |
rs574088254 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146098 | AGCCTCTGAGTGGCA[C/T]TGTCTAGTGTCCTCC | 286053 |
rs574092023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234265 | TGATTTTTGTCAACA[G/T]TCATCTAGACTAATA | 286053 |
rs574093061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168542 | CATGTTCAGCATCTG[C/G]TGAGGGCCTAGTTTC | 286053 |
rs574094592 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269032 | TGAACTCATGCATAG[C/T]TATCTTTGCTTATTA | 286053 |
rs574095333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351610 | TTGTTTTTCTACTTA[C/T]AGTTAGGAAAATTTT | 286053 |
rs574096772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217047 | AAGATTTATTAAGCA[C/T]CTATACTATATGCCA | 286053 |
rs574133444 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273345 | TACAGTAAACTTTTT[A/G]TATTTGTTGCATCAC | 286053 |
rs574153938 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114454 | TCATATATACCCACA[C/T]CCATGTTCATGGATT | 286053 |
rs574168023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097526 | CTCTCCCTGATAATT[G/T]AGACCTTTCCAAATC | 286053 |
rs574213767 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117706 | TTATTTTTAGAGACA[A/G]GGTCTTGCTATGTTG | 286053 |
rs574228776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234927 | CTGCCAGTCCTACAG[A/G]GCCCATTTCAAGTCC | 286053 |
rs574239409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189127 | TGTTAGAAATAGATA[A/G]TCAGTGTCACGAAGA | 286053 |
rs574282158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272828 | GTATATATATACACA[C/T]ATATATACACACGTA | 286053 |
rs574282550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232087 | AGTGCTGATGCCGGG[C/T]GCAGTGGCTCATGCC | 286053 |
rs574284647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240249 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 286053 |
rs574285691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336766 | CAAATTCTTTGCAAG[C/T]ACTTCTAGTCTACAT | 286053 |
rs574303163 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131854 | TGGTGAGGTGCCTTG[A/C]ACAAGTAGGTGCACC | 286053 |
rs574336750 | in-del | -/A | 0.274309 | 0.248815 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247725 | GCAAAATTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 286053 |
rs574345578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274728 | TGAGGTCAGCAGTTC[A/G]AGACCAGCCTGGCCA | 286053 |
rs574349747 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365833 | CTGCACCCCAGCCTG[C/G]GTGAAAGAGTGAGAC | 286053 |
rs574357944 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330336 | GTGTGCCACCACACC[C/T]GGCTAATTTTTGTAT | 286053 |
rs574362400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095121 | CTCCCAAAGTGCTGG[A/G]ATTATAGGCATGAGC | 286053 |
rs574363085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185233 | GCAGTGCACCAGCTG[G/T]AAGTTAATCTATCTG | 286053 |
rs574373515 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146902 | AAAGTATAAAAAAAA[-/C]AAAACAAAAAAAAAC | 286053 |
rs574387135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134285 | TTATATTAAATGTGG[C/T]TTAAATTATATAGTT | 286053 |
rs574397754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337579 | AAGTTTGACTTGCAA[A/G]TACTGTATGTTGACT | 286053 |
rs574398038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095488 | GGTCCCAGCTACTTG[A/G]GAGGCTAATGTGGGA | 286053 |
rs574417052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191658 | AGAATACAGTGCCTA[A/G]GAATTATGTTTCTGG | 286053 |
rs574421195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315627 | TAATAGAACCTTGCT[A/G]AAGGTTAGTTCCTTT | 286053 |
rs574422195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232877 | ACTAAAGGACTGTTA[C/T]GTGAATGAGTTATTC | 286053 |
rs574432907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203563 | GTTTTAAGTTCATAG[A/C]AAAATTGAGCATAAG | 286053 |
rs574433608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366384 | ACTCTATTAAAAATA[A/C]CAAAAATTAGCCGGG | 286053 |
rs574438871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140539 | GTGGTAGTGGGTGCC[C/T]GTAATCCCAGCTACT | 286053 |
rs574439616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104033 | TTTGCTCTTGTTGCC[A/C]AGGCTGGAGTGCAAT | 286053 |
rs574448287 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089892 | ATGGGTCTTTATTAC[C/G]TAGGTAAATCACCTT | 286053 |
rs574454887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281819 | TCCTGGCCTCAAGCA[A/G]TCCTCCCACTTCTGC | 286053 |
rs574472777 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177304 | TTCAACCCAGAGTGG[A/T]TTCAGATCTGTCTGA | 286053 |
rs574479445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268476 | CAAAAAGAACTATTT[A/G]GAGAATAAAGGAAAA | 286053 |
rs574481870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323475 | CAGTGGAATGGAATA[C/G]AGTCCAGAAATAGAT | 286053 |
rs574484809 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346671 | CTTTTCTTATAAGAG[A/G]TATTAAATGCAGGTG | 286053 |
rs574504506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294007 | CTAGGCAACCACTAA[A/C]TCTACTTTCTATCTC | 286053 |
rs574537388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345192 | AGGTGATCTAAATAC[A/G]TATGTGGAGTAGTTT | 286053 |
rs574553432 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207895 | AGAGCCGGAGCTGAA[C/G]AGCTCTTGAGGCCTG | 286053 |
rs574554401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307853 | CACCAGCACTGTGAG[C/T]TGGATCTCACCCACA | 286053 |
rs574559069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248161 | AAATTGAAACTAAAG[C/T]GTGAAAAGAAACAGT | 286053 |
rs574581468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191019 | GGGATTACAGGCACC[C/T]GCCACGCCACCTAGC | 286053 |
rs574604976 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148777 | GCTGGTGTGAAACCA[A/G]TAGTCTATTTTTCAT | 286053 |
rs574605092 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157347 | ATAGACAACTCTTAA[C/T]ATGTTTCTTATCAAA | 286053 |
rs574610001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184712 | TAATACAAGTTGATA[C/T]AAGTATAAACTTGTA | 286053 |
rs574627732 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341009 | TACGTGTTCCCTCAC[C/G/T]GGGCATGTGGTCGGG | 286053 |
rs574639202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287785 | TAACATTGGCAGCCC[A/G]ATCTCTTCCACCATT | 286053 |
rs574650532 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147080 | ACTTCCCTAATGCCA[C/G]ACTTGCAGAAGTGTT | 286053 |
rs574663652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248813 | GATAGGGTTTTACAG[A/G]GAAGGATATGGAGAC | 286053 |
rs574698596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241321 | AGACATTGGCTCACC[C/T]ATGAAAATGTATAAT | 286053 |
rs574704279 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289027 | AAACTCCTGAGCTCA[A/G]GCAATCCTGCCTTAA | 286053 |
rs574731775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254673 | ATTTCTAACATGCTA[G/T]AAGACTTTAAGCCTA | 286053 |
rs574758038 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323275 | GAATCCCAGCAGGGG[-/T]TTTTTTTGTAGATAT | 286053 |
rs574770668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118893 | TTTCATATGAATCAT[A/G]AGTATTTATTCTTCC | 286053 |
rs574773363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346925 | ATAACATGAAAGGGT[A/G]TATCTTACTAAAATG | 286053 |
rs574775387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142424 | CTCTCTTCTGTGTCA[C/T]GATGATGAGGGAATT | 286053 |
rs574780628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280601 | CCATCTGTTCAGAAA[C/T]GATCCTATTAATTTA | 286053 |
rs574803914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236235 | TGCTCAGAAGTTTCT[A/C]GTTATAGACCTGGTG | 286053 |
rs574808231 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338528 | AAGTGGAATAGAAAA[C/G]CAATGGTCCTTTTCT | 286053 |
rs574808685 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256721 | ATGAGGTCAGGAGAT[C/T]GGGACCATCCTGGCT | 286053 |
rs574814666 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353712 | ACATGGCGAAACCAC[A/G]TCTCCACTAAAAATA | 286053 |
rs574822441 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349303 | CCAAATTTTCCAAGC[A/T]CCAGCTCAGCCTTTC | 286053 |
rs574836142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244151 | CAGACTAATAGCAGG[A/G]ATCTACAATTATAGA | 286053 |
rs574846483 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314631 | CACTCCCTGAAAACA[A/G]CCAAGCCAGGTGATG | 286053 |
rs574863735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243784 | ATTACCTAATAGTCC[C/T]GCATGCTAAAAATAA | 286053 |
rs574871037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289427 | AGTCCTGCTTATTCT[C/G]TTGGACTCAGCTGTT | 286053 |
rs574881156 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340021 | TTTTTTGTTTTTTTT[G/T]TTTTTTTTTTTGAGA | 286053 |
rs574888072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212020 | TCTGTAAACGTTTAT[A/G]GATTGATTAGCCTAA | 286053 |
rs574911358 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258526 | CTCCATAGGAAAGCA[A/G]CCTCAGCCTGGACAA | 286053 |
rs574916629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262862 | TTTGGAAGTCCCAGG[A/T]GTTATATAAAGCAAG | 286053 |
rs574947197 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173875 | ACTCACTATGACCTT[A/G]GGCAAGATGCTGAAC | 286053 |
rs574963329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205099 | TTACCTGTAGACTTT[C/T]ACTCTTGCTGATCTC | 286053 |
rs574975507 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255848 | GTATGAATTCTGAAG[A/C]ATGAAGACCAGTCAG | 286053 |
rs574976051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269256 | CCACACTTGGCTAAT[A/T]TTTGTATTTTTAGTA | 286053 |
rs575026003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199643 | GGTGCTGAGAAGAAT[A/G]TATATTCTGTTGATT | 286053 |
rs575031152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249654 | GCAATCAGCCTGGCC[C/T]ACTTTGAGTTCTCTT | 286053 |
rs575032272 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098529 | AGGCAAGACTGAGAG[C/G]AGGGAGACCAGGTAG | 286053 |
rs575034676 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277903 | CCAGCTACCAAATAA[-/T]TTTTTTAAAAAGATG | 286053 |
rs575035275 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104059 | GCAATGGTGCGATCT[C/T]GGCTCACTGCAACCT | 286053 |
rs575037917 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280555 | GTGAGAAAAACTACA[-/T]TATTCACTATCATCA | 286053 |
rs575041537 | in-del | -/T | 0.457485 | 0.139462 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265160 | CTGGCTTTATTTAAT[-/T]TTTTTTTTGGTAGTT | 286053 |
rs575043329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170994 | CATCTGTCCCACTTC[A/G]CACCCTGCTTTGATT | 286053 |
rs575050533 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353362 | ATCCAAGGGAAAGAC[A/G]GCTCCTAGCCTTCTC | 286053 |
rs575063925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294765 | ACTCATCTGGGAAAT[C/T]TGTTTTGCGCTATGA | 286053 |
rs575067212 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276732 | TTTTGTTTGTTTCAT[C/G]CTAATAACCCAATGA | 286053 |
rs575074857 | in-del | -/CTTT | 0.00400639 | 0.0445774 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181304 | GAGCCTGTGTAAAGG[-/CTTT]TTCTTGAGAAAAGAG | 286053 |
rs575075843 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289017 | GGCTGGTCTCAAACT[C/T]CTGAGCTCAAGCAAT | 286053 |
rs575080101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206077 | TCTATAAAATGACGT[G/T]TTCAGAAAATGTTTT | 286053 |
rs575080802 | in-del | -/GTATCT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136079 | GCATGATGATGTCCA[-/GTATCT]TATAAACCTTTTTTA | 286053 |
rs575083676 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179488 | AACCATTAAAAAATA[A/G]TTAGTGCCCATTTGT | 286053 |
rs575096067 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338897 | TCTCAGTTTAGGCCA[A/G]AGATTTCTAAAGGAT | 286053 |
rs575097941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346420 | GTACTTACAACTCTC[C/T]AAAATAAGAGAATGT | 286053 |
rs575100973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204624 | GCTTGTTTATGTACA[A/T]TTTCCTCCTGCTGTA | 286053 |
rs575128455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213892 | ACTATTCTGACCATT[C/T]CCTTTTGTTTTATAT | 286053 |
rs575129513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213237 | CTGAAAGCAAAATGA[A/G]TCGTGCCATTGGAAA | 286053 |
rs575130799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276230 | ATGAGTACATTCTCA[A/G]TATAGCCTTCCAGGA | 286053 |
rs575132502 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228530 | AGACTTCCTGGAAGA[A/G]CTGACATTTGAGCTG | 286053 |
rs575139493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177965 | TGACTAGCTGTCCAC[A/G]TTAAATATCTTGGAG | 286053 |
rs575156819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264517 | GTTGAAACAATTCTC[A/G]TTCCTCGGCCTCCTG | 286053 |
rs575166374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230474 | ATTGATGTTCAAAGC[A/G]TGAACATCCCTTGGG | 286053 |
rs575168267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302519 | GGCTTTTACTTAGAG[G/T]TTAATATGGGGTGAG | 286053 |
rs575168382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263620 | CTGGGCATGGTAGCA[C/T]GCGCCTATAATCCCA | 286053 |
rs575187439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178859 | AACAGAGTGAGACTC[C/T]GCCTCAAAAAAAAAT | 286053 |
rs575204151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310845 | CCATGTAACGATTAA[C/T]GAGATATGTTTATTA | 286053 |
rs575216574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327784 | CAAAATATATGTATA[A/C]AATTGTTTTAGGATT | 286053 |
rs575232949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161650 | TAAAATATAAAAATT[A/G]GCCAGGTGTGGTGGT | 286053 |
rs575236844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271434 | AAGAGATAGGTGGAA[A/G]TAAGAGACAGAGTAG | 286053 |
rs575256145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301890 | ACTGGTCTCGAACTC[C/T]TGACCTCAGGTGATC | 286053 |
rs575257493 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123102 | TTATAGGGAAGATAA[C/G]AGAAATGGTTCTTGC | 286053 |
rs575272512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355130 | GGTCCCAAGCATTTC[A/G]GATAAGGGATACTCA | 286053 |
rs575289734 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114508 | CCCATCCATATCCAT[A/G]TATACATACATACGT | 286053 |
rs575295244 | snp | C/T | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125127969 | TTCCACTTGTGGTGT[C/T]ATGTCAGCGCTCAAA | 286053 |
rs575309990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223192 | GAAATCCCATCTGTA[C/G]AAAAAATACAAAAAA | 286053 |
rs575317502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115007 | ATGTGTCATATTTCC[C/G]TCACTGGACTGTATG | 286053 |
rs575323590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221349 | TTCCCTCACTCAGGT[A/G]ATCCTCCCACCTCAG | 286053 |
rs575349273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135845 | TAAGCTAGTGTTAGT[C/T]CTCCATTGTTGTCTT | 286053 |
rs575359623 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361812 | AGGGGTTGTAAGATA[A/G]AATTACTGTCTGTGT | 286053 |
rs575371870 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152872 | AGACCAGCCTGGCCA[A/G]CATAGTGAAACCCTG | 286053 |
rs575371964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222540 | CCCCCTTCCCCCAAC[C/T]TCTGGTAACCACCAT | 286053 |
rs575372292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231883 | CTCTTTCTTTTTAAC[A/G]CTTAAGACAGGTCTG | 286053 |
rs575390008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121324 | CTCTTCTTTTGGGCA[A/G]GTAATTTTGGACAAG | 286053 |
rs575393834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236886 | CTGTCACGTTTATTT[C/T]TCTTGTACCTACTAA | 286053 |
rs575416840 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093618 | ATCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 286053 |
rs575419719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310277 | ATTCCCAGCCCACCA[C/T]CTGTCAGATTTGGGG | 286053 |
rs575427019 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333628 | CACGCCATTCTCCTG[C/G]CTCAGCCTCCCAAGT | 286053 |
rs575445547 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169951 | TTTCATTTCCAAATA[A/G]CTGACTCTTTCTTAC | 286053 |
rs575446262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135210 | GTTGTAACCTGCTGT[A/G]CCTGGCCTAAAAAAG | 286053 |
rs575452583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270789 | TAAGGAGGGGTGAAC[A/G]GGCCCAGGTTGAAAA | 286053 |
rs575457360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297733 | ATAGCTAGTTGGGAG[A/G]CTGAGGTAGAAGGAT | 286053 |
rs575462295 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321793 | AAAAAGAAAAATCAG[G/T]CCAGGCACAGTGGCT | 286053 |
rs575463822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127511 | ATAGACTAAAATAGG[C/T]GTTTAAACCAGTTAA | 286053 |
rs575465180 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317286 | CACTGCAGCCTCAAC[C/G]TCCTGGGCTTAAGTG | 286053 |
rs575477682 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294824 | TCTGAGCTACTCAAG[C/T]ACTACTATGTGACAT | 286053 |
rs575503359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326875 | TCAGGAGAATCACTT[C/G]AACCCAGGAGGCAGA | 286053 |
rs575508244 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228025 | CTGGTTGTCTTTCAG[A/T]GGATAGCAGTTGATA | 286053 |
rs575511007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200923 | TTCATTAATTTGATC[G/T]TCAATCACTGATATC | 286053 |
rs575519556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362736 | CATCCAGCTCCCCTT[A/G]GGAGGGCTATTTGGT | 286053 |
rs575539652 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333999 | TTTTTTCCACTACTC[C/T]TTCATGCTCCTGGGT | 286053 |
rs575543316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318586 | AACATCTATTGTATC[A/G]GCCAAAAACTAGAAG | 286053 |
rs575551134 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113889 | TTAGCAGGTTCTAGG[A/T]TTGGGTAGAGGGTAG | 286053 |
rs575554334 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130488 | AATTATTTGAAATTC[G/T]GTAAAGAGTTTTGTT | 286053 |
rs575566179 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158276 | CAGGCCCTTTCTCCA[C/T]TGCATTACTCCAACA | 286053 |
rs575570533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201280 | ATTTTCAGCTGTTCT[G/T]CTCTGGTTTCTCCCC | 286053 |
rs575579837 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091994 | GGCAATGGGGAGGGT[A/G]GCAGGAGTTTCGCCA | 286053 |
rs575583968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220754 | AAGATTGAAATCCAC[C/T]TATTCATTTATGCTG | 286053 |
rs575589879 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132815 | TTTTAAATTGTTAAA[A/G]ATGGATACAATACTT | 286053 |
rs575597952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361026 | ATCTGTTAACAATAA[A/G]CCTATTTATTCTCTT | 286053 |
rs575601060 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306700 | CAATTTATGGACTTT[A/G]TCTTGATATCCAGTC | 286053 |
rs575607159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146576 | CAGCCATAAAAAATG[A/T]TGAGTTCATGTCCTT | 286053 |
rs575625597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247496 | TGGGGAGCCCAAGGC[C/T]GGTGGATTACCTGAG | 286053 |
rs575629398 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364068 | CCTGCCTCAGCCTCA[C/T]GAGTAGCTGGGATTA | 286053 |
rs575660961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312262 | AAACATTAACATTTC[A/G]GATGCTTAGAAAATG | 286053 |
rs575661039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188490 | TGAGTGGGTGTGGAC[C/T]CACTGTTGCCAGATC | 286053 |
rs575668451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139111 | AATGGAACTGTTCAG[C/T]GGTGGAACAAGCTTT | 286053 |
rs575680071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311699 | AGAAATCTGAAGAAT[A/G]TAATGTGTTGCTTGG | 286053 |
rs575681991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278821 | CTTTTACTAACTATG[C/T]ATAATATTGATATGC | 286053 |
rs575684809 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222317 | TACCTTGCAGAATAA[C/T]TAAATCAAGTTAATT | 286053 |
rs575691084 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137670 | GACAAAGTCTTATGA[C/T]ATAGAAATGTTTATG | 286053 |
rs575708240 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358029 | CTGAGGGAACTTCAA[C/T]CACACCTTCAAAACA | 286053 |
rs575708894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283936 | AGGTGGGCAGATCAC[A/G]AGGTCAGGAGATGGA | 286053 |
rs575717743 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095002 | GGCTGCAGGCCCGCA[C/T]CACCACATCCAGCTA | 286053 |
rs575723557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181118 | CTGATGGAGAGCAGC[C/T]GCAGCAAAGTGATAA | 286053 |
rs575723690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319190 | CACTCTGGTCATCCT[C/G]AGCACAACTTTAAAA | 286053 |
rs575743293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145565 | TTTGATTAACGAAAG[C/G]AAGGGCTGGCTGTAA | 286053 |
rs575744712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278267 | GTGCCACATTCCTGC[A/G]GAGATATTGAGCAAT | 286053 |
rs575756815 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290722 | ACAAATATGGTTGCC[A/G]TGGCACATGTCTGAA | 286053 |
rs575774076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290171 | TTAAAAAAAACTCCA[C/T]TTTCTGGTAGTAGCC | 286053 |
rs575782205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341143 | TGTAGTTAGAGTAAC[C/T]GGAGAGCTGCAATCC | 286053 |
rs575788772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350435 | GAAACAGAAAAGGCC[A/G]GTGTGCCTTGAGCAC | 286053 |
rs575817796 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272275 | CGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 286053 |
rs575823871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300191 | TTTTTTTATTTTGAG[A/G]CAAGTCTAGCTTGGT | 286053 |
rs575859772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238492 | TCCATTATAACTCTT[A/G]AGCAAATCCTGGAAT | 286053 |
rs575865926 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192463 | CAAATGAAATGTTTC[A/C]AGTTAATATTGTAAT | 286053 |
rs575875642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237917 | TGCACATTCCAGTTA[A/G]AGAGTACTAAGCTAT | 286053 |
rs575876952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356416 | CCACTGCAACCTCCA[A/G]CTTCTGGGTTCAAGC | 286053 |
rs575880352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144032 | GATAAATGTGTGTGG[A/G]CGTGATAGGGAAAAG | 286053 |
rs575882477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151812 | CATAAGGCAGTTAAG[A/G]TGGGAACATAGCAAC | 286053 |
rs575883057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246781 | TTGAAAAATAAAAAC[A/G]TTATGTACAAGTCTA | 286053 |
rs575883618 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332209 | TATTTTGCCAGTCAC[C/T]GATGCTAAGTCAAAA | 286053 |
rs575900991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252391 | AATTAGCTGGATGTG[G/T]TGGTGGGTGCCTGTA | 286053 |
rs575914814 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123743 | GCAATTTTGCTGTAA[C/T]GAAATTCATTTCAGC | 286053 |
rs575920149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245916 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 286053 |
rs575949790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351066 | GATTGGATGTGAGGA[A/G]TGAAGAAAAGGGAAT | 286053 |
rs575975573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116424 | AATTATTATTATTTC[C/T]ATTTTACTTGACCCA | 286053 |
rs575987204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335704 | GGTTCCTTATTTGAC[A/C]GATCATTGACATGGT | 286053 |
rs575988227 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166504 | ACTCCTGACTTCAAG[C/T]GATCTCCCCGCTTTG | 286053 |
rs576010736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292349 | CACTTGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 286053 |
rs576014502 | in-del | -/TA | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194001 | AGTGTTGCCTCTTTG[-/TA]TATATGTTGAAAGAG | 286053 |
rs576017741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241147 | CCTTTGAGCACGAGG[A/T]CAGTCCTCAAAAAGC | 286053 |
rs576018060 | snp | A/G | 1.64811e-05 | 0.00287059 | missense | NSMCE2 | GRCh38.p7 | 8:125151243 | ATCGGCAACTAAACC[A/G]TTATGTAAAGGCTGT | 286053 |
rs576020914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343723 | AACTGCTGCCGGGCA[C/T]AGTGGCTTATGCCTG | 286053 |
rs576034039 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360038 | GGAGGTACAGTTAAC[A/G]ACATTTGACGACTGA | 286053 |
rs576042479 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268780 | AGTGCATGAGCCAAG[A/T]GAGGAAGTAATTTTA | 286053 |
rs576051654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232982 | CAAAAGAATGGTCAC[A/G]TTCCAGGGTTGTAAC | 286053 |
rs576053336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286860 | TCTGGTTCCTTTGCA[C/T]CCTAAGAAAATCATA | 286053 |
rs576069142 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182346 | TGATTTTATAAAGTT[A/T]GCTTATCTGCTTGGC | 286053 |
rs576070435 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323991 | GGAAAAAAGATTTTG[-/A]AAAAGATACTGAAAT | 286053 |
rs576081627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169229 | CCTGCTATTCCTACC[C/T]GTTCTTCGATTTTCT | 286053 |
rs576104293 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295556 | CATTGGGCTGCACAC[C/G]CCTGTCTCTGCTTAG | 286053 |
rs576110218 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219161 | CCACATATTTGCTAT[C/T]TGGGGTCTGGGGAGG | 286053 |
rs576143509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169999 | TAGCTCCTTTCTTAC[A/G]GCCTGCTCTGATATC | 286053 |
rs576160711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320649 | ATACCCAGCAAAATA[C/T]ATTTTTTAAAAAAAG | 286053 |
rs576170044 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160527 | AAAGGATTGTTCAGA[A/G]TCAGGGGAACTGGGC | 286053 |
rs576172480 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293019 | TAAATCTGTCCCAGG[A/G]GGCCTGGTTTAGGTC | 286053 |
rs576176947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329742 | GCCAGTTTACCTCTC[C/T]GGACCTCGGTTTCCT | 286053 |
rs576178525 | in-del | -/CT | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353166 | TTCACATCAGCTGAA[-/CT]CTGTTATTCATCCAG | 286053 |
rs576215852 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126281 | GGAGGCCGAGGCAGG[A/G]GAATCACTTCAACCC | 286053 |
rs576219322 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223759 | CCATATATTTCTTGG[C/T]CACTTATGTGTCTTT | 286053 |
rs576228964 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214503 | CAGTACAGGACCCTA[C/T]GTGAAAGAAAGGAGT | 286053 |
rs576242430 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291831 | GAGTAACTAACAGGA[G/T]TTTCTATATAAACAA | 286053 |
rs576245426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196689 | GTCTTTACGGTAGCA[A/T]GATTTATAATCCTTT | 286053 |
rs576249624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095159 | CCAGCCAGGTTTTAG[A/G]TAATCAGTACACATG | 286053 |
rs576259659 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252719 | GATGGTTTAAAAATC[A/C]ATCATGCTTATCCAT | 286053 |
rs576266328 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280464 | CAGTTTTACTGTCCT[C/G]TGTGCAAACTGCTTA | 286053 |
rs576273560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215751 | TTCAGCTTTCTACAT[A/G]TGGGTAGCCAGTTTT | 286053 |
rs576289132 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167398 | AAGGCCCGGCATGGT[C/G]GTTTATGCCTGTAAT | 286053 |
rs576301265 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148997 | AGCAACATATATATG[C/T]TGGTACCAAGCCATA | 286053 |
rs576310034 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243395 | CCTTAAGCTGAAAGA[C/T]GTTCCAAAAGGAAGA | 286053 |
rs576313208 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305237 | TTTAATACATTATTT[G/T]ATTTAGTCATCATGA | 286053 |
rs576319751 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247962 | ACAGTAAACAGACAA[C/T]TATTATAATAAGTGC | 286053 |
rs576327373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139863 | CTTTTCCTTCTGTTC[A/G]CCTACACTTACTGAA | 286053 |
rs576328796 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300620 | ATGGGGTACAAAGAT[A/G]CGAAGAACATCGTCC | 286053 |
rs576335965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262154 | GTATAGGCCGGGTGC[A/G]ATGGCTCACACCTGT | 286053 |
rs576337451 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146025 | GGAAAAATAATTTTC[-/T]TTTTGTTATCAGATT | 286053 |
rs576337829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163068 | AGAAAGAATGTTAAA[A/C]AGTTTATACTTTCTA | 286053 |
rs576358741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167221 | AGTTGTGTAGTAAAG[C/T]GAGGTTTATCTAAAT | 286053 |
rs576358973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174318 | GTTCAGTAAATATTT[A/G]CTGAATGAATAAATG | 286053 |
rs576362554 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307740 | TAAAGGGGTTTTGAC[A/C/T]AAGCAAGTGTCGTTT | 286053 |
rs576400026 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241179 | TTGAATTTTATGGCA[G/T]TTCGGATTTTGTATT | 286053 |
rs576401701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104092 | GCCTCCCGGGTTCAA[A/G]CGATTCTCCTGCCTC | 286053 |
rs576404705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358327 | AACAGAGCTAGACTC[C/T]GTCTCAAAAAAAAAA | 286053 |
rs576404779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155404 | CAATCCAAAGACTTA[C/T]TGTGAAAATTAGGCC | 286053 |
rs576414550 | in-del | -/TCTT | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231869 | CACATTTTCTTTATC[-/TCTT]TCTTTTTAACACTTA | 286053 |
rs576420933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324365 | ACTACACAAATGTTC[A/G]TAGCAGCTTTATTTC | 286053 |
rs576423772 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261537 | TTCAGCACACTTCAG[A/G]CATTTTAATAAAACT | 286053 |
rs576450673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305917 | TAACAATCAGTTGTA[A/G]TACAGGCTAAATGTT | 286053 |
rs576451037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298891 | TATTGATGGGATTAA[C/G]TTTGGGGTGATATTA | 286053 |
rs576451157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119717 | TTTTTAAAAGACATA[A/G]AATTTTACGTCTTCT | 286053 |
rs576467662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352246 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCA | 286053 |
rs576475432 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101197 | ATGGTAGGTACTCAA[G/T]ACTTATGAGTGAAAT | 286053 |
rs576480239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254881 | CACGTAAAGGAATAT[A/G]GTTGTTTTACAACAT | 286053 |
rs576489896 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142522 | TGTGTTTGTAAAGAA[A/C]CCCTGACACTTACTA | 286053 |
rs576500069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091438 | ATGATTTCCCCCTAA[A/G]CGGAGACGAAGAGCT | 286053 |
rs576501514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162505 | TTTTTTTTTCTGTGC[C/T]TGCCCACTGAATAGC | 286053 |
rs576509145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210982 | AAGTGATTCACCTGC[C/T]TTGGCCTCCCAAAGT | 286053 |
rs576530134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203083 | GCTGCAGCTATCACT[A/G]TGTACTCTGTGGGCC | 286053 |
rs576536325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124716 | CTCCTGGGGTCAAGC[A/G]ATCCTCCTGCCTTGG | 286053 |
rs576548621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365086 | TGGGTGACTCACTGA[C/T]GTCTTTAGCTGCAGC | 286053 |
rs576571264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218530 | AATTCTCATGCCTCA[A/G]CCTCCCGAGTAGCTG | 286053 |
rs576578143 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180910 | TGGGCACTGGTAATA[C/T]CGTGATAAATCAGAC | 286053 |
rs576582673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125104 | GATTTTCTGCATACA[A/G]GATCATGTCATCTGT | 286053 |
rs576582785 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258460 | CCATTCACCCCCGCT[-/C]CCCCCCACCCCACTT | 286053 |
rs576610718 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102249 | GTTTACAGCAGTTTT[A/G]TTAATATTTTCCTGT | 286053 |
rs576623747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255520 | AGAATAAAGGGTGGC[A/G]TGTTCTAGGCAGAGG | 286053 |
rs576630821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192518 | TGAATATTATATGTA[C/T]ATGGTAGCAAATAGG | 286053 |
rs576633878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345269 | TGCTTTTGTACAGAA[A/G]TGGAACAGAGAATGA | 286053 |
rs576642870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307050 | AATGGGAGCCCAGCC[C/T]ATTGTAAATCACTCA | 286053 |
rs576643592 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365497 | AGAGTAACATTTTCC[A/C]GATGTAAACCAAACA | 286053 |
rs576653999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212560 | TGGAGGGTTCAGGTA[C/T]GTGTTCAGTACCAAA | 286053 |
rs576672979 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097760 | GGCAGAAAGGAGTTA[C/T]GTTTATTCTGGAATA | 286053 |
rs576679525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323545 | AAGACAGTTCCATGG[C/T]TTTCCACAAACATGC | 286053 |
rs576693903 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183416 | TATTTTTGTTCTTTT[G/T]TTTAACATCACAGCT | 286053 |
rs576699809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198265 | AGCCTTATCTTGTGC[C/T]GGTTTTCAAAGGGAA | 286053 |
rs576699843 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204398 | CTCTTTCCCGAGAGG[A/G]CACTATACTGTGACT | 286053 |
rs576705814 | in-del | -/AA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341921 | AAAAAAAAAAAAAAA[-/AA]CCTGTCTCTGCCCAT | 286053 |
rs576713105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224866 | CTGCAGAGTCCATGC[C/T]CTTTACTATTACGTA | 286053 |
rs576720769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126851 | TTCTCACTTTATTTA[A/G]GATTGATGTGAGAAT | 286053 |
rs576734159 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291959 | ACCCAGGCTCTTTCC[A/T]TCTTGTGGTTCTGTC | 286053 |
rs576735039 | snp | C/T | 3.33946e-05 | 0.00408609 | utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125366925 | ACCAGCAGCCTACCT[C/T]CTACCCCAGCTGTCT | 286053 |
rs576744205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359562 | GGTCTCAAACTCCCG[A/G]GCTCAGGTGATCTGC | 286053 |
rs576761815 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198550 | AGCCTACTTGATCGT[C/G]GTGGATAAGTTTTTT | 286053 |
rs576770605 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140524 | AAAAATTAGCTGGGC[A/G]TGGTAGTGGGTGCCT | 286053 |
rs576780984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366463 | GAGAATGGTGTGAAC[C/T]CGGGAGGCGGAGCTT | 286053 |
rs576791263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127359 | GCCATGTGTGTTTCT[G/T]TGTGGGGGGAGATTG | 286053 |
rs576792068 | snp | A/G | 1.7412e-05 | 0.00295055 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357856 | GTGGAGCCTTCCCTA[A/G]TGGTAGTTACTCAGA | 286053 |
rs576795267 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212113 | TTTTTATTAGTTTCT[G/T]CCTTTGTGTTAATTA | 286053 |
rs576833976 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107406 | ACCATGTTGTCCAGG[A/G]TGGTCTTGAACTCCT | 286053 |
rs576848276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360234 | CCAGCAATACAGCCC[C/T]GTGGAAGTGTCCAGG | 286053 |
rs576858587 | in-del | -/T | 0.116138 | 0.211142 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247019 | TGATTAAATTCTGTA[-/T]TTTTTTTTTTTCTTA | 286053 |
rs576870990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269479 | TGGAGCAAAACCATG[C/G]CACTATAAAATGACA | 286053 |
rs576894164 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178053 | ACAGCATCCCAGTTG[C/T]CAGCCCCTCTGCCAT | 286053 |
rs576900666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308960 | GAAAGAATTGTGTTA[C/T]GAGGCCGGGCACGGT | 286053 |
rs576901347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171098 | TCATTTTCTTTAGGT[C/T]TCTGGTTCAGATGTC | 286053 |
rs576916022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288311 | GAGGCCCTCAGCCTC[A/G]AGATAATTTTTTTCT | 286053 |
rs576921903 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281278 | TTGTGGTAGTGCTTT[A/C]ATATTGGAGACATTC | 286053 |
rs576933772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142539 | CCTGACACTTACTAG[C/T]TTGTATCATGTACTG | 286053 |
rs576963288 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338309 | AAAAAGCTGCCTTTT[A/T]TATAGAAGTTCTTGG | 286053 |
rs576965413 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319668 | CACTGCAGAAGAGAA[G/T]ACTAGTGAACTGGAC | 286053 |
rs576984224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347069 | GTGCTGTGTCAGCTA[C/T]CTACAGCTTGCTATT | 286053 |
rs576984516 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354282 | TTTGCTTTGGAAATA[C/G]GTTGGCTACCAGTAA | 286053 |
rs577001374 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168121 | CTATGAAAGATTTTA[-/T]TTTTTTTTTGTGGAC | 286053 |
rs577004441 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133852 | AAAACGCCGTTTATG[A/G]TTTTTAACTTTGTAT | 286053 |
rs577013578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270164 | GAACATCCTTATATG[A/T]CTTACTAAAGAATCT | 286053 |
rs577020088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104661 | GAGCTCTTTATCTGC[A/G]TAGCTCCCTCACTCT | 286053 |
rs577027764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235100 | AAAATACAAAAATTG[A/G]TGTGTTGGCACACGC | 286053 |
rs577027771 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346268 | TTTTTCAGTAATCCA[A/T]ATTGGAAATGTTGGG | 286053 |
rs577070711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353821 | CCGGGAGGCAGAGGT[G/T]GCAATGAGCCAAGAT | 286053 |
rs577073997 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160052 | TACACAAATAGCTAC[-/A]AAAAAAATTTTAACG | 286053 |
rs577088087 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143517 | TATATGAGTCATGTT[A/G]AATTGGAGTCAGCAA | 286053 |
rs577088364 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276401 | CCTCTTCCTTACTCC[A/G]GACTAACTGGAGGAC | 286053 |
rs577099236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234386 | TCTGTATTTTTCAGA[C/T]TGTGAAAACTAGGCA | 286053 |
rs577103167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120660 | ACAATTAGGCCTGTC[A/G]GCAATTGACCTTGGA | 286053 |
rs577104570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097783 | CTGGAATATCAAATA[A/G]TTAAGGTTATATGAA | 286053 |
rs577107164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212496 | CTTGAACAACAAGGT[A/G]AAAAGAGCAAAATGG | 286053 |
rs577134131 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250552 | CACTTATATTCTCAT[G/T]AATTCAGATTTGTCT | 286053 |
rs577142702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347715 | GTGGGTATAGACAGT[A/G]GATATTATGAGATTT | 286053 |
rs577166397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332717 | ATTTTTCTTTCCCCT[A/G]TCCCCTTCAGGGTTC | 286053 |
rs577199872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159546 | TAGGTTTGTGTAAGT[A/G]CACTCCGTGATGTTC | 286053 |
rs577225351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297408 | GACCTCCTGGGACAG[A/G]CAGCTCATTCCATTT | 286053 |
rs577226692 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183335 | TTGGAATGTTTTGCA[A/G]TCATGATGAGACTTT | 286053 |
rs577234089 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279750 | TTTAAAATGTTGACT[A/G]TTCATACTTGCCTAT | 286053 |
rs577236373 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338597 | CCTCAGAAGCAATAC[A/C]GAGAAGAAAAGAAAA | 286053 |
rs577236551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243056 | TGGAAAAAAAATCAC[C/T]AGACATGGAAATGTC | 286053 |
rs577256702 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283797 | CCCAGGGCCCATTTT[A/G]CCTCTTTGTTTCAAC | 286053 |
rs577276763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150520 | CTCACTGCAACCTTC[A/T]TGTCCTGGGTTCAAG | 286053 |
rs577276835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333321 | ACTGCAGGCACATGC[C/T]ACCATGCCTGGGTAA | 286053 |
rs577295391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290819 | AAAAACCCAAGGAAG[C/T]ATAAAGTAAAAAGGA | 286053 |
rs577295624 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308139 | CGGAGGCATGGGAGT[C/T]TATATAACCTTCTCT | 286053 |
rs577296776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236999 | GGCACTCAGTAGTTA[C/T]ACATTTCCTCTGAGG | 286053 |
rs577306307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187290 | GACAAGATGACTAGG[A/G]TAGTGATGGTGGTGA | 286053 |
rs577311227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099843 | GGCTGGTAACCAGAG[A/G]GGTAAGTGGGAGGAA | 286053 |
rs577324351 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158933 | CAGTAGTCACTGGTT[A/G]TCTACAGTTTCACTT | 286053 |
rs577324765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289584 | GAGCTCATTTAGAAC[A/G]GAGACCAAGTCGTGC | 286053 |
rs577357260 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136742 | TTTTTTGAGGCTTCT[G/T]GTAGGTTTAGGTGTT | 286053 |
rs577402396 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263566 | ACCAGCGTTGCCAAC[A/G]TGGTGAAACCCTGTC | 286053 |
rs577412249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158060 | GAACATCTCTCTGGA[A/G]GAGGGACTGATATTC | 286053 |
rs577446840 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356240 | TCTGTGTGTATGGGG[A/G]GGGGTGTTCTGGAAA | 286053 |
rs577454648 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092052 | GAGCCGGGGGTCCGT[C/G]TACCCGGATTATGGT | 286053 |
rs577474795 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236926 | CATAGTAGAGGGTCT[A/G]TAAATACTAGTGAAA | 286053 |
rs577482341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257724 | TATTTTTAGTAGAAA[C/T]GGGGTTTCATTGTGT | 286053 |
rs577490751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339077 | ACATGGGGAGAGGAT[A/G]CATTTTAAAAAGCTC | 286053 |
rs577494610 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100574 | TTTTTTTATTTTTAT[G/T]TTTTTGAGACCGCGT | 286053 |
rs577495240 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135608 | TCAGTATTTTCCTTC[-/T]TTTTTTTTTCTTTGC | 286053 |
rs577495823 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263364 | TGCTGGCTCATGGAA[-/C]CAGGTGTTCTTAGGA | 286053 |
rs577508771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303198 | GCCTCCCTCTGTGAA[C/T]CTGCAGTTCAGCTTT | 286053 |
rs577516939 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255774 | GGATTGAAGCTGTCT[A/G]ATCAGGTTTGTGTTT | 286053 |
rs577526392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199685 | GTTTTGTAGATGTCT[A/G]TTAGGTCTGCTTGGT | 286053 |
rs577533605 | snp | A/G | 3.29859e-05 | 0.00406102 | missense | NSMCE2 | GRCh38.p7 | 8:125151276 | AATCTACAATAAATC[A/G]TGTAAGTTTATACCA | 286053 |
rs577550204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252101 | TAGCTGAGATTGCCC[A/G]GGAGAGTATAGTCAG | 286053 |
rs577561188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252797 | TATTTAAGCAGTGCA[C/T]AGATTAGATTAAATG | 286053 |
rs577577989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201361 | TGGGGTTTTGGTGTG[A/G]ATGTCCTTTTTGTTG | 286053 |
rs577587518 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285698 | GTAATAGCAGACCCA[A/G]TATAATAGCTAGCAT | 286053 |
rs577587531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289072 | GGGATTTACAGGCAT[A/G]TGCCACCACACTTGG | 286053 |
rs577603905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320146 | ACACCACCACACTCC[A/G]GTCTGGGCAACAGAG | 286053 |
rs577614691 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355656 | AGTGAGCCAAGATCG[C/T]GCCATTGCACTCCAG | 286053 |
rs577625156 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162220 | TCTCAGGAAGTTGGT[A/T]AAAAAAATTTTAATT | 286053 |
rs577629845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164622 | ACTGTTATATGTAAC[A/G]GTTATATTAAAAATA | 286053 |
rs577656432 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254199 | ATCTCTATTGAAACA[-/CT]CTGTGTTTCAGTCGT | 286053 |
rs577702915 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216558 | AGAATTGCTTGAACC[G/T]GGGAGGCGGAGGTTG | 286053 |
rs577718690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125362038 | CAGCAGTCACCTTTG[G/T]GTTTGCCCTGTGCTG | 286053 |
rs577722156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108393 | GCCTGTAACAGTAGA[C/T]GAAAGACTTGTAGAA | 286053 |
rs577726783 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121615 | GTGAATGTATTTTTA[C/T]ATTTTATGACCTAGC | 286053 |
rs577741619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348558 | CCATAATTCCCACGT[A/G]TTGTGAGAGGGCCCC | 286053 |
rs577743062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313016 | GTAGAGGATGGGTCA[A/G]TAGGTGTGCAGCAAA | 286053 |
rs577750484 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361032 | TAACAATAAGCCTAT[G/T]TATTCTCTTAAAAAT | 286053 |
rs577751227 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172989 | TGGAGTTATTTCTAT[C/G]TTCCATTATCTTTCA | 286053 |
rs577771544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229692 | TTTCCCCAGTTCTAC[C/T]TTGTGTATAAGGATA | 286053 |
rs577779881 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107498 | GGCCTGGCCTATCAA[A/G]GACATTCTTAAATGA | 286053 |
rs577787930 | snp | A/T | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195603 | ACTTAGCATTCATTC[A/T]TTCAACAGATGTTCA | 286053 |
rs577791870 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122223 | TATGAAATGTACTAT[A/G]CTAGAAATACAAAGA | 286053 |
rs577798135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214722 | ATGATATATTTGTTG[C/G]AATTGATGAACCAAT | 286053 |
rs577804958 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153495 | TACATCACTTTATGT[A/G]CTTGAAGCTAAGGAT | 286053 |
rs577823447 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303901 | TGTCCCTAAGATGCA[G/T]GTCACCTACTTCTTG | 286053 |
rs577855982 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298762 | ATTTAAATACTATGT[A/G]GTTTGTTGTCACCAG | 286053 |
rs577857083 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225795 | TTCACTTCAAGCATC[A/G]TTGCTTTTGGCAATT | 286053 |
rs577874225 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125136239 | CTTGAGAAAGAGAAT[G/T]GGCAACATCATGGAA | 286053 |
rs577876416 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355193 | CTGGCCTAGGTGATG[G/T]CCCACAGTCATCAGT | 286053 |
rs577891735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195443 | AGGATCCATACAAAC[A/G]TATCTTAGCATAGTC | 286053 |
rs577913533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356453 | CCTGCCCTAGCCTCC[C/T]AAATAGCTGGGACTA | 286053 |
rs577916750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220900 | TAATATATAGTTCTT[C/T]ATTCTGTGGTTAAAG | 286053 |
rs577953780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195819 | GTACTGTCTTTCAGA[A/G]TTATTTGCCTTGTAT | 286053 |
rs577958469 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153972 | ATATAGGATTAAGTA[C/T]AGGCTACTTAAATTA | 286053 |
rs577962848 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094463 | TAATCTTTTCCCTAC[G/T]CCAGAATTACAGAAG | 286053 |
rs577984097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333214 | TCGCTCTGTCGCCAA[A/G]GCTGAAATACAGTGG | 286053 |
rs577989556 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116586 | CGTGTGTGTGTGCGT[A/G]TATGTGCACACATGG | 286053 |
rs577992893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363646 | AGGAAGAAGAGAGGA[A/G]GAGGAAGGAGAAGAG | 286053 |
rs578008431 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120746 | GGTGGGAGTTATGAA[A/C]CTAGTTTGGAGGAGA | 286053 |
rs578029445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221422 | CTAAGTTTTGTATTT[A/T]TTGTAGACACAGGGT | 286053 |
rs578041011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259997 | CGAGGCAGCAGCCTG[A/G]TGAAACAAAAAGAAA | 286053 |
rs578044909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272811 | TATATATATACACAC[A/G]CGTATATATATACAC | 286053 |
rs578062807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358555 | TTCTTCCATGACCAC[A/G]GAGGACCATGCTCTG | 286053 |
rs578064317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174467 | GTAAATAAATCATTC[C/T]GGTTGGTCATCGTAT | 286053 |
rs578067422 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124119 | GATTTGCCTATTTCC[A/G]GCATCTCATATAAAT | 286053 |
rs578073066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246060 | ATAAAAAGAGGTATA[C/T]AACCATAGACGTGTT | 286053 |
rs578075989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278291 | GAGCAATCTTTGGGG[C/T]CCTTGAATGGCACCA | 286053 |
rs578089681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145357 | AATCAGGGATTATCT[A/G]TGCCCTTTGGACTTG | 286053 |
rs578090715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272362 | CTAGAAGTTTAATGT[C/G]CATCTTATTATGTCA | 286053 |
rs578094515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094989 | CCTGAGGAGCTGGGG[C/T]TGCAGGCCCGCACCA | 286053 |
rs578106749 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181198 | AGAGTGGCTCCTTTT[C/T]TCCCCCAAGGAGGTG | 286053 |
rs578137198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334097 | ATAATAACTCCTGAC[C/T]TTAAAGGGCCATTGT | 286053 |
rs578141912 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203969 | GGATTCCCTAGTCCT[C/T]ATCGTGTAATTTACA | 286053 |
rs578143118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131124 | TTGTCATAGTCTGGA[C/T]TCTATTACAGGATCC | 286053 |
rs578153709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266936 | TATTTATAAATAAAG[A/G]TAATCTGAACATTTG | 286053 |
rs578196243 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137722 | AGGTAGTTAGGCGAA[C/T]GGACTCTGTTATTTA | 286053 |
rs578202785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144551 | AAGGACCGTATTGCT[A/G]CAGGCTTACTGCCTA | 286053 |
rs578226711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094237 | AGCACTTGCTGTTTG[G/T]GAAGCACTGCTAACA | 286053 |
rs578257045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239494 | CACGCCTGTAGTACC[A/G]GCCACTCGGGTGGTT | 286053 |
rs745313180 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281396 | CTAAAATTTCAACAC[A/G]TTATACAGCAAGGTT | 286053 |
rs745319054 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125360448 | AAGGCCAGAGCCCGA[C/T]TTCGTTCTGCTCACT | 286053 |
rs745330578 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267498 | TACGCTAAGAAATCA[A/G]TACTTTGCCAGGCAT | 286053 |
rs745353564 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327265 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs745360542 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232465 | TGAGCAAATAAGCTT[C/T]AGGTGCTTTTAGAAT | 286053 |
rs745369547 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262466 | ATTTTGTGAAAGTAT[A/G]TGAGTCAAACTTTCC | 286053 |
rs745371791 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346835 | ATTTAATAGCTGGAG[A/G]CAAATTAATAACATG | 286053 |
rs745375838 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218802 | TCGCAACAACATGAA[C/T]AAACTTGACACTAAT | 286053 |
rs745380113 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091767 | ACTTCCGCCCCTGAC[G/T]CCCCAGGCGGTCACA | 286053 |
rs745380171 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289969 | CCACAAAAGCTGGTG[C/T]ACACATGTGATAGTG | 286053 |
rs745410079 | snp | A/G | 1.64925e-05 | 0.00287158 | utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102329 | TAGGTACTAATTTCA[A/G]GATGCCAGGACGTTC | 286053 |
rs745414727 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312576 | GTTGCAGTGAGCCAA[G/T]ATCACGCCACTGCAT | 286053 |
rs745428944 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184425 | ACACATTATTTGGAT[A/G]GACAGTCAAACCTTA | 286053 |
rs745432142 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170932 | TTTTACTACTCTGTG[C/T]AAAACCTTCACACAT | 286053 |
rs745440282 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361820 | TAAGATAGAATTACT[A/G]TCTGTGTTGAGGTAT | 286053 |
rs745446571 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171469 | CGCTCCTCAGCTTCA[G/T]TTCCTAATCAATAGC | 286053 |
rs745462191 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203348 | CCTTGCATAACTAAT[A/G]TCTAGAAAGAGGAAG | 286053 |
rs745484391 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126210 | AACTTGGTGAAGACT[-/C]CCATCTCTTCTAAAA | 286053 |
rs745489033 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268359 | GGCACTTCTGTTGGT[C/T]GTTTGAAGGAGAAAG | 286053 |
rs745506177 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300382 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGAACTCA | 286053 |
rs745526695 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110633 | AGGGATTTGATTATA[A/G]GCAGTCTGACTTCAT | 286053 |
rs745543452 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301306 | AACAGCGTCCCAAGT[A/C]GTCATCTAACCCGAG | 286053 |
rs745573164 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235775 | AAGTCCTCAAGAGCA[G/T]GAATGGTTACATACT | 286053 |
rs745576907 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254574 | TGACCCACATGGGTT[A/C]TTTGCTTTTTCTTTT | 286053 |
rs745598940 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115015 | TATTTCCCTCACTGG[A/T]CTGTATGTCCTTGAG | 286053 |
rs745626468 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352748 | CTTTTACCAGACTTA[G/T]CACAAAGTTTTGTCT | 286053 |
rs745632715 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175189 | TACCCTGTGCATGAC[A/G]AATTGGGTTGGTGGT | 286053 |
rs745636789 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303788 | GGGATGAATGATTCC[C/T]TCAGTTGCTCTCAGC | 286053 |
rs745646658 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223716 | TAATTTGCATTTCCC[A/G]GGTGTCTGGAGAAGT | 286053 |
rs745662897 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166958 | AGGATGCAGGGAGTT[-/A]ATAAAGGTGCCACTG | 286053 |
rs745663644 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331566 | ACTATAGATTTTCTC[C/T]TCCCTGAAGTTTAAA | 286053 |
rs745665139 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210270 | TAAATGTTATGTGTT[A/C]GCTATTCATTACTGT | 286053 |
rs745680372 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300621 | TGGGGTACAAAGATG[C/T]GAAGAACATCGTCCC | 286053 |
rs745682864 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244581 | AAAGGTACATCTTTA[A/G]AAATATCATAATGGA | 286053 |
rs745695917 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238570 | CTTCATTAAACAGCA[-/T]TTTTTTTTCCTTTCT | 286053 |
rs745701407 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304908 | AAAGAGAGAGAAAGA[A/G]AGGAAAGAGAGAAAG | 286053 |
rs745710878 | snp | A/G | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090876 | ATGCAAGCTGCATAT[A/G]TTTTCCAGAAAAGTT | 286053 |
rs745714248 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127161 | GTTCCTGGTTTGATG[-/A]AAACAGTTACATGCT | 286053 |
rs745744973 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339476 | AAGCTTCTGTATAGC[C/T]TACATTTCAGGAGAC | 286053 |
rs745750681 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151080 | ACAAAATTATTTAGA[C/T]CATTGACTGATGTAG | 286053 |
rs745768361 | snp | A/C | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195606 | TAGCATTCATTCATT[A/C]AACAGATGTTCATTT | 286053 |
rs745799518 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100807 | CTCAGGTGACCCTCC[C/T]GCTTCAGCCTCCCAA | 286053 |
rs745800868 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293175 | CATTCTAAGAATGCT[A/G]TTACTATTATACTCA | 286053 |
rs745808084 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137648 | CATAAATCTTAAGAG[C/T]GAATTTGACAAAGTC | 286053 |
rs745812211 | snp | C/T | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093561 | AAATAAATAAATAAG[C/T]AAATAAATAACATAA | 286053 |
rs745819381 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280194 | AGAACGTGGATAATA[C/T]GAGCTAGTTAGAAGA | 286053 |
rs745836991 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152499 | TTAAAAGAACAAGGC[A/T]GACTTTATAGAAGAA | 286053 |
rs745844527 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245534 | TTATCAAAATTAGAG[A/G]AAAATTGTTGCCTTA | 286053 |
rs745855830 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175317 | TCTAGGATCAGTTGA[-/G]GGCAATTCCCTCTGG | 286053 |
rs745857608 | in-del | -/CTTTTGA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162872 | AAGATTCACATTTAC[-/CTTTTGA]CTTTAGTCATCTTTT | 286053 |
rs745889719 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118776 | TTCCAGGAATGAGGA[C/T]TATACCTCTCACCTT | 286053 |
rs745908694 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125151223 | GGTTGAATTTGCTAC[A/G]TTGGATCGGCAACTA | 286053 |
rs745917404 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142829 | TGGTCTCGAACTCCT[-/G]GACCTCAGGTGATCC | 286053 |
rs745918001 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342524 | GGTGAGAGGAAGGAA[A/G]GCTTAGAGGCAAGGA | 286053 |
rs745959531 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199113 | GCTAGTGGTCTGTCA[A/G]TTTTGTTGATCTTTT | 286053 |
rs745969481 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282263 | GGATTACAGGCGCAT[A/G]CCACTACACCCAGCA | 286053 |
rs745970838 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234384 | TATCTGTATTTTTCA[C/G]ATTGTGAAAACTAGG | 286053 |
rs745984376 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249038 | TAGCCGAGTATGGTG[A/G]CACATGCCTTTAATC | 286053 |
rs746002802 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296099 | TAAACATTTACTACA[C/T]GCTAGGCATTATAAT | 286053 |
rs746006378 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154827 | TTTCTCAGTTTCATA[G/T]TGAGAACAGAATGAT | 286053 |
rs746019398 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348302 | TTTCTGATTACATTA[C/T]ATTAATTCAACCTGT | 286053 |
rs746026180 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328044 | AATCATTTTTTAAAA[C/T]TGTTTGCTTTAGTGA | 286053 |
rs746029626 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168109 | ATGGGTTTAATTTCT[A/G]TGAAAGATTTTATTT | 286053 |
rs746040470 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211773 | TTTTGGTCTCTGCCA[-/C]TTGTATATCCCAGAT | 286053 |
rs746047576 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156253 | TTTAAGACATTTTAC[C/G]TCTTAAAAGAATTTT | 286053 |
rs746050171 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293437 | CTTTCCCCATATAGA[G/T]CTAATTATTCTTTGT | 286053 |
rs746079528 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113890 | TAGCAGGTTCTAGGA[G/T]TGGGTAGAGGGTAGA | 286053 |
rs746084293 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284369 | GCTAAGGCTGCCATC[C/T]ACTTCAGAGAAGGAG | 286053 |
rs746093950 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269597 | CTGATGAATGTGAAC[A/G]TTCAATGATCATAGC | 286053 |
rs746126840 | in-del | -/AAGG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304940 | AGAAGGAAAGAAAGG[-/AAGG]AAGGAAGGAAGGAAG | 286053 |
rs746134658 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106870 | GCGTGGTGGTGGGCG[C/T]CTATAATCCCGGCTA | 286053 |
rs746137811 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227069 | GAAACACCTGAGGCC[A/T]CTCAGGGTCTGTATT | 286053 |
rs746163860 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097386 | TGTCTACACTATATT[C/G]CCAAAGAATGAAATC | 286053 |
rs746187267 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239923 | CACCTGAGAAGTAAG[A/T]AAGTGTGTCGCCCAC | 286053 |
rs746191620 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199760 | CTTGTTTATCAGTCT[A/G]ATATTGACAGTGGGG | 286053 |
rs746192805 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288776 | GACAAGTCTTTTCCC[C/T]AGTCTTTATTTTTTA | 286053 |
rs746205792 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274185 | GCTTGGCAGATTGGA[A/G]ATCCCAAGCACAAAA | 286053 |
rs746229050 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268469 | CAACAAGCAAAAAGA[A/G]CTATTTGGAGAATAA | 286053 |
rs746240046 | in-del | -/TA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217361 | ATTTATTTATTTATT[-/TA]TTTTATTTATTTATT | 286053 |
rs746253814 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125357262 | CGGAACAGAAGGAGT[A/G]GATGAAGATATAATT | 286053 |
rs746285873 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319163 | GAAAAAAATTAACCA[C/T]AGATTAAACACCACT | 286053 |
rs746287230 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145395 | GGGGTGGCAGTGCGG[A/G]GGGGATAGCTAGTTA | 286053 |
rs746288034 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176922 | ACTTATTGTGAGTTT[C/T]CTCATATCCTTGCTG | 286053 |
rs746302482 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320627 | AAAACTTTCAGACTA[A/G]AATTCCATACCCAGC | 286053 |
rs746305420 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365037 | CAGAGAAGACCACAT[C/T]GAAGCAGAGCCGTGG | 286053 |
rs746316996 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355812 | TCCCATCATCCCATT[C/G]AAATGTTGTCTATCA | 286053 |
rs746332504 | in-del | -/TTGT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340679 | AGGCCACTGTGTGTC[-/TTGT]ATCAAGTAACCTAAT | 286053 |
rs746334529 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309071 | CCAACATGGAGAAAC[C/G]CTGTCTCTACTAAAA | 286053 |
rs746349612 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147786 | TTCTGTGTTTATCCC[A/T]TTTTCCCCCTCCAAA | 286053 |
rs746354142 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275928 | TTATGTCTTTAGCCC[A/G]ACCTAAATTCCAGCC | 286053 |
rs746362978 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132457 | GAATCCTAAGGAGAG[C/G]CATGTATCTTAAGAC | 286053 |
rs746380622 | in-del | -/AT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330972 | ACCTCTTTCACACAC[-/AT]ATGATGTGAAAAAGG | 286053 |
rs746390786 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134094 | GAGAAAGCAAATTAT[A/G]GTACAAAGCAATCAT | 286053 |
rs746394099 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125308260 | TAAATACTGAGTCTC[A/G]GGCCTTTGCTCTTTG | 286053 |
rs746396874 | in-del | -/ATTG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331687 | TCAAAATCAGACCAC[-/ATTG]TTAGAAGTTATTTCA | 286053 |
rs746404683 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117640 | CCAACTCAGCCTCCC[A/G]AAGTAGCTGGGACCA | 286053 |
rs746415153 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227157 | ATGAACCCCTGCCTT[A/G]ACCTTGCCCATCCTC | 286053 |
rs746427815 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212049 | AAGTGGGCAAAGTCC[A/C]TCTGTCTCTATAATT | 286053 |
rs746432532 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244992 | TAAGGGATTTTAAAC[A/C]TTGAAATTGGCCAAG | 286053 |
rs746445100 | in-del | -/AGA | 4.94531e-05 | 0.00497234 | cds-indel | NSMCE2 | GRCh38.p7 | 8:125357253 | AGAAGCTGACGGAAC[-/AGA]AGGAGTGGATGAAGA | 286053 |
rs746454191 | snp | A/T | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363352 | TACCAAAAATTTTTT[A/T]AAAATTAGCCAGGCG | 286053 |
rs746495437 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347873 | AAAGGAGGAAGAACA[C/T]TGATCAGAATGTTGA | 286053 |
rs746545242 | snp | G/T | 1.64857e-05 | 0.00287099 | missense | NSMCE2 | GRCh38.p7 | 8:125357769 | ACCTATGAAGAGGAC[G/T]CCATTGTTCGCATGA | 286053 |
rs746549371 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239975 | CTCATTGCTGAGGCC[A/G]CTGTCAGCCTTTGTT | 286053 |
rs746552708 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213372 | AATGTGATTTCACTG[C/T]CCATATTGCTCATAT | 286053 |
rs746564569 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172417 | TCAACCTCTGTGTAC[A/G]CTTTTTTCCAAGACT | 286053 |
rs746583295 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332647 | CTAATCCAGATATAT[G/T]ACAAGTTTTCTTTTA | 286053 |
rs746584602 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160714 | CAGACAACAAGTAAA[C/T]ATTCACAGTTTTTAA | 286053 |
rs746594029 | in-del | -/AT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330973 | ACCTCTTTCACACAC[-/AT]GATGTGAAAAAGGTG | 286053 |
rs746595104 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191945 | CCACAAGGATAGCAA[A/G]TACGTTCACAAGGAA | 286053 |
rs746598158 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159808 | CTACTAAAAATACAA[A/G]AATCGGCTGGGTGTG | 286053 |
rs746603568 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145590 | CTGTAATAAATAAAC[C/G]CTCACAGAATGGCTT | 286053 |
rs746603896 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334987 | TCTCAAACTCCTGGC[A/C]TCAAGCAGTCCTCCC | 286053 |
rs746625563 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288858 | GGAGTGCAGTGGCTC[A/G]ATCTTGGCTCACTGC | 286053 |
rs746632615 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183366 | GTTTTTACTGTAGAC[-/T]TTAACCAGTAAGCAT | 286053 |
rs746637435 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256415 | AATATAAGGAGGAGG[A/G]TAATGCAGGGGCAAA | 286053 |
rs746644993 | in-del | -/TG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203233 | TTATCGTAAATGTTG[-/TG]TGTGTGTGTGTGTGT | 286053 |
rs746659217 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302381 | GGAGTTGGCCTGGCA[C/G]ACATTCCAGGAGTGA | 286053 |
rs746663269 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276346 | AGTTTTCCTGCCCTT[C/G]TTTGTTGGTCTTACC | 286053 |
rs746692960 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098698 | TGAGGGGAGGAGGAG[A/G]AGGATCAAGTATGAA | 286053 |
rs746711505 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235441 | AAGTGAAAAGATAAC[G/T]CCTCTGACCCCAATC | 286053 |
rs746714633 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288266 | CATAATCCTGTCCTT[A/G]CTGCTTCTCTGACTG | 286053 |
rs746714914 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112657 | GAAAGATAAATAGTG[C/G]TTGATCTCACTCGTA | 286053 |
rs746715873 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117453 | AAGATACCATAATTT[G/T]CCATGTCTCGATATC | 286053 |
rs746719213 | snp | A/G | 1.65551e-05 | 0.00287702 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102308 | GTTTCATTGTGTTTG[A/G]AAACTTAGGTACTAA | 286053 |
rs746722404 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186838 | ATACAAACCTAACAG[A/G]TATACTACACTCATT | 286053 |
rs746727335 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241541 | AAGTTAAGAGAGTTA[C/T]AGATTTATGTGTCAT | 286053 |
rs746738000 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155845 | GAGGTAACAAATCCA[A/G]CCACTATCATGGGGG | 286053 |
rs746740384 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280368 | GTGTTTCTAAACTAA[C/T]GAAATGTCCTTTCTA | 286053 |
rs746752207 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340329 | GAAACTAGGTTAAAA[C/T]TTCAAAGCCAATGCT | 286053 |
rs746760936 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294470 | CCAGCACATGTTATT[G/T]TCTCTTTTTTATTGT | 286053 |
rs746773112 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211887 | ATCTTAGATAATCTT[A/C]TATTTTCATTGACTT | 286053 |
rs746800746 | snp | G/T | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195746 | ATTTCTTTATAACTC[G/T]AAAACAAATATGCCT | 286053 |
rs746819706 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152615 | TTGATAAGCCTTTCT[A/G]TCTTTAACTTTCATA | 286053 |
rs746823323 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182855 | GCAATGTAATTTTTT[A/G]TACCAAAAAAATTTT | 286053 |
rs746825643 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262061 | GAGATTGCACCGCTG[C/T]ACTCCAGCCTGGGTG | 286053 |
rs746839549 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246614 | ACATATTTATCACTC[A/G]ATACTGTCAAACTTT | 286053 |
rs746842231 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357537 | AAAGTCATGGCCTAC[A/G]GGCCAAGTGACAGTA | 286053 |
rs746849544 | snp | C/G | 1.64825e-05 | 0.00287071 | missense | NSMCE2 | GRCh38.p7 | 8:125151209 | ATGGACAAGGCAATG[C/G]TTGAATTTGCTACAT | 286053 |
rs746886782 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312682 | TGCAGTGCCACTAGA[A/G]CAAGGATAGCAGACT | 286053 |
rs746899476 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138825 | AGACTTGAGACTTTC[C/T]GTTTGACCCAGGAGG | 286053 |
rs746900222 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300203 | GAGACAAGTCTAGCT[C/T]GGTCGCCCAGGCTAG | 286053 |
rs746912832 | in-del | -/AATT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220372 | ACATGATTAAAAAAA[-/AATT]AAGGCATTATCATTT | 286053 |
rs746928600 | snp | C/G | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090967 | GTCCCTTGTAGTGCA[C/G]AAAGACAGTAAAACT | 286053 |
rs746935308 | snp | A/G | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362120 | CTGCGAGGCCTGAAG[A/G]GCTGACTCCTGCACA | 286053 |
rs746951573 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154439 | TTGTCTCTCAAGAAA[A/T]CAGGGCTACTATACT | 286053 |
rs746974185 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313838 | CAAAATGAAAAATCA[A/G]AGGGACCCAAAATGA | 286053 |
rs746981221 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203701 | TAAGTAAGTAATTGA[C/T]GTCTTGGAGGTGAGA | 286053 |
rs746981853 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218912 | TTGGTGATTTATCCC[C/T]TGTAACCAATATTTT | 286053 |
rs746982046 | snp | C/T | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092020 | CGCCACCCTCAGGGA[C/T]ACTCCACGGGGACTC | 286053 |
rs746999748 | in-del | -/TTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121677 | TTTTGTAGACTCTAA[-/TTT]AATAGGCAACTTAAT | 286053 |
rs746999984 | in-del | -/ATAATA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275003 | AATCTGAAGATGATA[-/ATAATA]ATAATAATAATAATA | 286053 |
rs747003444 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233771 | TCTAGGTTGGTTTCT[C/G]TCAGAGACATCACCA | 286053 |
rs747031945 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268461 | AACAACAACAACAAG[C/G]AAAAAGAACTATTTG | 286053 |
rs747056689 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251484 | ACTTAGAGTTTACAT[A/G]CAACAGAAGGAATAG | 286053 |
rs747072516 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345420 | TCATCTTTTTATTGT[A/G]GTAAATTTGTACATG | 286053 |
rs747080024 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201228 | CTGGCGAGGAGCTGT[C/G]ATCCGTTGGAGGAGA | 286053 |
rs747124436 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141845 | CAGTGTTAGCTGCCC[A/G]TTCTTCTTGCTTTGA | 286053 |
rs747131853 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157484 | ACTTGGAATGTGTCT[A/G]TTTCTGTGATTACTG | 286053 |
rs747162248 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272310 | TGAGCCACCGCGCCC[A/G]GCAAATCTGCAGTTT | 286053 |
rs747169066 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329608 | TAGCTTGTTCCGATA[C/T]ACTGGGACAAACCTT | 286053 |
rs747196736 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188747 | CTTTCAGGATACTGC[C/G]AACTAAGGCCAAAAT | 286053 |
rs747200219 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTTTCTGAATAACTTT | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125195881 | TTTCCTGAATAACTT[lengthTooLong]TTTTTTTTTTTTTTT | 286053 |
rs747209265 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285849 | ATTACCCCAGTTTAC[A/G]GATGAGGTAACTGAA | 286053 |
rs747215854 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174353 | AATAAATAATGCATG[G/T]TTCTGTGAATTTCTG | 286053 |
rs747232304 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142681 | GCTATCTTGGCTCAC[A/C]ACAACCTCCACCTCC | 286053 |
rs747237342 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140971 | GAAAGACACCTGGCC[A/G]TGAAGATTTGGAGGC | 286053 |
rs747274464 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095538 | GGTTGAGGCTGTAGC[A/G]AGCATGATCATGTCA | 286053 |
rs747278715 | in-del | -/AACC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221155 | CAACAAAGTTTAAAT[-/AACC]AACCATGTCAGGTTG | 286053 |
rs747282790 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222604 | AGATTCCACGTGTAA[A/G]TGAGATCATACAGTA | 286053 |
rs747285394 | snp | A/T | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128846 | GCCTTGTGATTACAT[A/T]AGGTCCACCCAGATA | 286053 |
rs747343849 | snp | A/G | 0.000233684 | 0.0108068 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182284 | GCTTTGCTTTGGTTC[A/G]GCTTTTTGAAATTAG | 286053 |
rs747361114 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099386 | AGATATCTAGGGGAC[C/T]AGTATCATGGCAGAG | 286053 |
rs747361455 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228874 | GGCCACTCACAGACG[C/G]AAGTAGAAACTCAGA | 286053 |
rs747371290 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192924 | TATGTTTTCTTTGGA[A/G]TTCCATACTTTAAGG | 286053 |
rs747381638 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293107 | GATTCTGCAAATTTA[A/T]TTATACAACAATAAT | 286053 |
rs747401844 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320338 | GGAAGGAAGGCAGGC[G/T]GAAAATTTTCCAAAT | 286053 |
rs747423002 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343653 | AAAAATTAAAAAAAA[A/C]AATTAAAGTATGACA | 286053 |
rs747430528 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213130 | TGGCTTTGAAAGAGT[C/T]GACCTGTATGAAAAA | 286053 |
rs747442256 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356801 | TTGATTATTGCTTTG[C/T]ACCATGAGCTGTGCA | 286053 |
rs747450486 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168217 | GTAGTGAATGGCAGC[A/G]AAACACTGTTCTTTG | 286053 |
rs747468822 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178845 | ACTACAGCCTGGGCA[A/G]CAGAGTGAGACTCCG | 286053 |
rs747521895 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118969 | CTTTTAAAAGACTTA[C/T]ACATATTGTGCGCAT | 286053 |
rs747528323 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127338 | GGGGAGTACATGATA[A/G]TAAGGGCCATGTGTG | 286053 |
rs747538846 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156511 | TACTAGAAGCCTGGT[A/G]AGGGAGAATATTTTT | 286053 |
rs747538863 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168972 | CATTTTTGTGTAGAT[A/G]AGGAAGCTAGGGCTT | 286053 |
rs747555914 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258132 | ACAGTAAGTGTGGGT[A/G]TAGATGTAAATAGTT | 286053 |
rs747594039 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155612 | TCCTACTTCTTAAAC[-/A]GGGGTTATCTCTCTT | 286053 |
rs747621104 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335343 | CAGAACAGCCCTACC[A/G]GACAGGTATTTTCAT | 286053 |
rs747622116 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160084 | TGAAATAGTTTGACA[-/G]AGACAATAAAAACGT | 286053 |
rs747624353 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241739 | TACTCATAGTGTAAG[G/T]TGAAAAGAAGTGAAT | 286053 |
rs747631519 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242691 | AACTACAGAGTAGTT[A/G]TGGAAGAGGAGGGGG | 286053 |
rs747647875 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163144 | GGCCGAGGTGGGAGG[A/G]TCGCTTGAGCCCAGG | 286053 |
rs747660498 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206556 | AGTAGTATCTATAGG[A/C]TTTGTCAAATATTTC | 286053 |
rs747663199 | snp | A/G | 3.2963e-05 | 0.00405961 | missense | NSMCE2 | GRCh38.p7 | 8:125357291 | TTGTGACCCAAAGTC[A/G]GACCAACTTCACCTG | 286053 |
rs747670713 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193169 | GTATAAAGTTGAGTA[G/T]TCAGTATGATTACAA | 286053 |
rs747675814 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227393 | TGACTGCAGCTCAGA[A/G]AGCAAGTCATGCCAA | 286053 |
rs747704595 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261378 | GAGATCCAATATCAG[-/A]AAGCCTTTATTATTT | 286053 |
rs747723212 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336389 | GGTGGTCATTTTCCC[A/G]AGATCAAATAGCTAG | 286053 |
rs747732055 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148413 | CTTTTGTAGCATTTT[A/G]AATATCTTAGGCACA | 286053 |
rs747737568 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322074 | TTTTTTGGATTTTGA[G/T]TTTTAAGAGATCTTT | 286053 |
rs747745308 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278093 | CATAGCCCGTGAAAT[A/G]TTTGCTGGATTTTAA | 286053 |
rs747754516 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146891 | CCCTAAAACTTAAAG[-/T]ATAAAAAAAACAAAA | 286053 |
rs747760020 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194302 | TTTGTTTTTTCTATA[C/T]ATAATTTTAATTTTT | 286053 |
rs747763841 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264152 | GTAAGCCCTAAAAGC[A/T]GTAGATGTGCTTGTT | 286053 |
rs747767334 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357057 | AGAATGAGGTACCCC[A/G]TAGTGTTCTCTGAAA | 286053 |
rs747785735 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291227 | TTATTCATCCGAAGA[G/T]ACTGGAGGTGGTAAT | 286053 |
rs747814821 | snp | A/C | 1.64879e-05 | 0.00287118 | missense | NSMCE2 | GRCh38.p7 | 8:125357724 | CAGGAGGAAATGAAG[A/C]AGCCAGTGAAAAATA | 286053 |
rs747827360 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323263 | GAAACCACAATCAGA[A/G]TCCCAGCAGGGGTTT | 286053 |
rs747831086 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105727 | GGGCATGGCTGTGGT[C/G]TTATAAAACTTTATT | 286053 |
rs747839325 | snp | A/G | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362331 | TGGAGACGAAGGAGA[A/G]ACAAGGTCCTTCCCA | 286053 |
rs747846989 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100482 | GCAGTAACTCCCATG[C/T]TGCTTTAATTATCAG | 286053 |
rs747860360 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309544 | GCTGGACAACATAGC[A/G]AGACCCCTGTCTCTA | 286053 |
rs747884264 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356326 | CTTTTAATTTTTTGG[-/T]TTTTTTTTTTTTTTT | 286053 |
rs747888615 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260115 | GCCACAGTCAGTGTC[A/G]AAGCCAGAGCTGGAA | 286053 |
rs747902305 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184969 | GATGCCTGTTTTGAC[A/G]GAGTAAAGGCTGAAG | 286053 |
rs747911635 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282722 | ATATACTGTGCTTGG[A/G]CACCAGTAATAATGC | 286053 |
rs747911764 | snp | A/T | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092123 | TTACCCTCCTGTCCG[A/T]GACGCCATCTCTCCA | 286053 |
rs747915329 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268590 | GACCTGGAATCAGAG[A/G]GAAAAATCAGGGCTA | 286053 |
rs747919765 | snp | A/G | 1.65296e-05 | 0.00287481 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102528 | TGTCTACTTTGAGGT[A/G]ACACTGTGTGGTGGT | 286053 |
rs747936592 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324169 | AAGTTTTTAAAAACA[C/G]GACAAAAACTGATCA | 286053 |
rs747947600 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284811 | CCAAATGAAAATAGA[C/T]TAATCAAAACAGTGA | 286053 |
rs747974779 | in-del | -/TT | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125362695 | AGGTCTTTCTCATTC[-/TT]GAGCCTGCAATTCTG | 286053 |
rs747987782 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102423 | CTTGAAAAACTTCCA[A/G]GCCTGTATCAACTCT | 286053 |
rs747992485 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171873 | ATATCTGCTCTGTCC[A/G]GAGTGGTGTGGTAGT | 286053 |
rs747992498 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185913 | CATTTGGTCTATTTT[A/G]TTGACGTACACAAAG | 286053 |
rs747995998 | snp | A/C | 3.34571e-05 | 0.00408992 | utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125366931 | AGCCTACCTCCTACC[A/C]CAGCTGTCTGTTGAG | 286053 |
rs748003328 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288120 | CGTGAGCCACCATAC[C/T]GGCCGATGTTTTAGG | 286053 |
rs748007391 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126172 | CAGATCACTTGAGGT[C/G]AGGAGTTCGAGACCA | 286053 |
rs748021524 | snp | C/T | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093150 | TATTTCTCACAGTTC[C/T]GGGGCCTGTTTCCTG | 286053 |
rs748026811 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327815 | TAAAGGCATGACTGT[A/G]TTAGGTAACTAATTA | 286053 |
rs748041172 | snp | A/G | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363435 | TGCTTGAGCCTCAGA[A/G]GCAGAGGTCACAGTA | 286053 |
rs748064325 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117222 | TCAGCTTCTTTGGCT[A/T]TTTATTTTTTTTTCT | 286053 |
rs748072484 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301479 | GGAGGTGGCGGTGGG[A/G]TGGTGGTGAGGATTA | 286053 |
rs748079621 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269338 | GTGATCACCTTCCTC[C/T]GCCTCCCAAAGTGCT | 286053 |
rs748084441 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152776 | AAGAATTGAACTCTT[G/T]GCTGGGCGCGGTAGC | 286053 |
rs748084464 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114346 | ATTGCCTATAGGTAC[A/G]TGATACACAGTAAGC | 286053 |
rs748084953 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231561 | CTACCATAGCACTTT[C/T]GCACACTATAGATTG | 286053 |
rs748107216 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111974 | GAGTCTAGTTGAGTC[A/G]GGGAGATTTCTTTTT | 286053 |
rs748117916 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222741 | TTGTATATGTATATA[C/G]CACATTTTTTAAATC | 286053 |
rs748136453 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095740 | TCTCTACTAAAAATA[C/T]AAAAATTAGCCTGGC | 286053 |
rs748139155 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160854 | TTATTAAACTATCTT[C/G]CTTACATCTTTAAGT | 286053 |
rs748140956 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204813 | TCTGCCCCCACTACT[A/G]TTGCTGCTCTACTTC | 286053 |
rs748145468 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127307 | GGAATGGCACTGAGA[A/T]TGTGTGCTGAGGTTG | 286053 |
rs748148697 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188956 | TGGAAGAAGACAGAT[A/G]AGAAGTAAACCAAGG | 286053 |
rs748160628 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299522 | CACTCACTATGATAG[C/G]AACAGCATGGGGGAA | 286053 |
rs748163563 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270538 | GCATGTGTTGAATTG[A/C]TTTAAATAGAAGCAA | 286053 |
rs748163772 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220943 | GCAGGGCTTTCTCTA[A/G]CTTGGGCCCTGTGTG | 286053 |
rs748174509 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272336 | AGTTTCTTCATTTTA[G/T]CACACTTACACTAGA | 286053 |
rs748179839 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238297 | TCTTTCCTCACAACA[C/G]TCCCAATAGCATTTC | 286053 |
rs748181949 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203288 | TAGTACCCTCATCTC[C/T]TGTCAACCTGTTTGC | 286053 |
rs748186209 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256835 | GGAGGCTGAGGCAGG[C/T]GAATTGCTTGAACCT | 286053 |
rs748220890 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287772 | TCCATTTACTCCTTA[A/T]CATTGGCAGCCCGAT | 286053 |
rs748234465 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129228 | TAGGGTTTGGGTAAA[A/G]TTGCAGGTAGTGAGA | 286053 |
rs748263990 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353168 | CACATCAGCTGAACT[C/G]TGTTATTCATCCAGC | 286053 |
rs748287112 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144039 | GTGTGTGGACGTGAT[A/G]GGGAAAAGAGGGGGG | 286053 |
rs748298385 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175698 | CCCTCCCAGTGAAAC[G/T]ATGGTTATAAGGCAA | 286053 |
rs748299842 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137407 | GGCTGACCCTATTCG[C/T]ATCTTTTTCTTGGTA | 286053 |
rs748313145 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190062 | TGCTAAAAATCTTAA[A/G]TGTCACAACCAAGAT | 286053 |
rs748324674 | snp | A/G | 1.64925e-05 | 0.00287158 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125366867 | CCATAACAAGAAAAG[A/G]CATCGTCATTCCGAG | 286053 |
rs748350505 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273406 | TGGAAAACAGTGTGC[A/G]GTAACTATGGTAACA | 286053 |
rs748351832 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338005 | CTCAGGATAAAATGT[A/T]GATAATGATTGAAAG | 286053 |
rs748374377 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130388 | TCCCTCTACATACTG[C/T]TTTTTGGAAGCAAGT | 286053 |
rs748379743 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305261 | ATCATGATAACCCTA[C/T]GGAGTAAGTAGTATC | 286053 |
rs748396226 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306397 | GCTGTTTTCACCACT[C/T]ATTGTCCCATCTTGG | 286053 |
rs748425399 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116250 | ATTTTTGGACCAAGG[G/T]CACAGCTAACAAATG | 286053 |
rs748436884 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168363 | AAAGGAAGAAGACTG[A/T]CTAGAGTCTTTTCTG | 286053 |
rs748444426 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220181 | AGGATCAGTTGATCT[C/T]ATTTGGGCAGGAGTC | 286053 |
rs748447938 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210526 | AGAAATACATACTAT[A/G]GAAGAACTGTAGAAA | 286053 |
rs748462530 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358498 | CTTTAAATATATATA[A/G]TATACACACACACAC | 286053 |
rs748469780 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125121193 | GAAGTTATAGGTAGC[A/G]TGCTCAGTAGATGAA | 286053 |
rs748469980 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137406 | AGGCTGACCCTATTC[A/G]TATCTTTTTCTTGGT | 286053 |
rs748497590 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230749 | CACAAACTGGGCAAA[A/G]TAGATTTGCAAAACA | 286053 |
rs748506989 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140617 | TCATGCCACTGCACT[C/G]CAGCCTGGGTGATGG | 286053 |
rs748519394 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180329 | CTCTCCATGTTTTCT[A/G]AAACTCTCTTTAATG | 286053 |
rs748529315 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314897 | AATAGCAGAGAAGTA[A/C]ACAAAGCGAGATGTT | 286053 |
rs748535853 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317232 | AGACAGGGTCTCACT[C/G]TATCACCCAGGCTGG | 286053 |
rs748549359 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202295 | TCACCAGTCTTCTGC[A/G]TCGATCACGCTGGGA | 286053 |
rs748563885 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310965 | TCGCAAGGGGGAAAA[C/G]CCAGTGCTAATGATG | 286053 |
rs748573859 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192824 | AGGGGAAAGGCTTCA[C/T]CTGTAAGGCTGCCTG | 286053 |
rs748575269 | in-del | -/AC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272805 | CATGTGTATATATAT[-/AC]ACACACGTATATATA | 286053 |
rs748589932 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298613 | CAGGCAGAGTTGTTA[C/T]AGTAATTAAATGGAA | 286053 |
rs748593816 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157567 | ATTAAGGTTGTGTTC[A/G]GTAACATTTTGCCTA | 286053 |
rs748611571 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169220 | TCAGTAAAGCCTGCT[A/G]TTCCTACCCGTTCTT | 286053 |
rs748612673 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171748 | GTGACCATAAGAATA[C/T]CAGTAATAATAATAG | 286053 |
rs748629612 | snp | A/G | 6.6949e-05 | 0.00578533 | missense | NSMCE2 | GRCh38.p7 | 8:125182116 | AGGTGAAAGAAGAAC[A/G]TCCAGAAAAAATACC | 286053 |
rs748637273 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316461 | GGCAGTACGTGCATT[A/G]GTCAGAAGCTGGAAT | 286053 |
rs748640559 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284864 | CTTATGAAAAGAGAA[A/C]CTAATTAGTAGGCAT | 286053 |
rs748653394 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108834 | TGAGTTGTTTACAGT[C/G]TAGGTAGGAAATAAG | 286053 |
rs748657066 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285942 | ATTCAGGTTTGACCT[A/G]ACCAAAACTTGAGCC | 286053 |
rs748663883 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122389 | AAAATGGTAGTTATT[A/T]CCTTCTACAACTATT | 286053 |
rs748683687 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158777 | GGTTTAGGCCTTTCC[C/G]CACTAATTGGCAGTG | 286053 |
rs748684886 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107517 | ATTCTTAAATGAAAC[A/T]AGCATTTGTTTTACT | 286053 |
rs748698360 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159620 | CAGTGCATGACTATA[C/T]AGGGTTTGGTACTAT | 286053 |
rs748699304 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265055 | AATATTTTATGTAGT[A/G]TCTTAAAAATTAAAG | 286053 |
rs748703699 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108368 | TTTAAGGAAATTGGA[-/G]GGTAGATCAGCCTGT | 286053 |
rs748709064 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290184 | CACTTTCTGGTAGTA[A/G]CCCATGTCTTATGCT | 286053 |
rs748712851 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337617 | ACAACAGGTTTGGCC[A/G]GGCGTGGTGGCTCAA | 286053 |
rs748725357 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252752 | CTAAATTATTTTAGA[A/G]TGAAAGCATACCTTT | 286053 |
rs748727474 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237521 | CTACATAATTAACTC[C/G]ACTTGCTGTGCTTCC | 286053 |
rs748762825 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100689 | GCCCAGCTTCCCGAG[C/T]AGCTGGGATTACAGG | 286053 |
rs748771860 | in-del | -/T | 1.66424e-05 | 0.0028846 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357357 | CTGAAAGAAACACGA[-/T]TCACTTCACAGAGGC | 286053 |
rs748776788 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229292 | GATGAACTGAAAGCA[G/T]TGAAGGCAACCTATG | 286053 |
rs748782022 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230877 | CAGCATGAGATACTA[C/G]TACAGGTGGACAGGT | 286053 |
rs748799348 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322373 | AGAAAGAAGGAAAAT[A/C]ATATGATCATCTCAA | 286053 |
rs748799388 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194352 | GAATTGTACAGTGTG[G/T]AGCCTTTTGAGTGGC | 286053 |
rs748840790 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150913 | TAATACAAGTCTTTT[C/T]TTCTTTCCAACCTAC | 286053 |
rs748845662 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345576 | GTAGGGAAGATAGAG[A/C]AGTAAACAAATGATT | 286053 |
rs748855120 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361455 | AATAAAATGAAATTG[A/C]ATAGAAATGGGTCAT | 286053 |
rs748866003 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137441 | ATGTGTTTAAAATAA[A/G]TGTAGAGATATGCTA | 286053 |
rs748870186 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265508 | TTACAAGCATGAGCC[A/G]CTGCACCTAGTCTTT | 286053 |
rs748880855 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311063 | GGGGTCAAAGTTACA[C/T]CGCAGTAATTACTGC | 286053 |
rs748912986 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157904 | TATAATAGGAAAATA[A/G]GATTTTGTGGTCAAA | 286053 |
rs748921051 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122705 | GTTTGTTGTACATTC[G/T]TCCATCTAAACAGCA | 286053 |
rs748932468 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303871 | TGTTTAAAGATATAC[A/C]TTGTTTGTATAACGT | 286053 |
rs748936070 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130542 | AGGATCAGCTATTTT[C/T]CCAAGGGCCCTGGTT | 286053 |
rs748968563 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170608 | TGATGGGGTTTCACC[A/C]TGTTGGCCAGGCTGG | 286053 |
rs748972747 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298797 | AGACTCATGTCAACA[A/T]TGGTTCAGAATAAGC | 286053 |
rs748983931 | snp | C/T | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090557 | ATTTTCTTTTACAAG[C/T]GCCGGTAACTTCATT | 286053 |
rs749013324 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187425 | AGACATAACCAGACT[C/T]TCTTGGGTGAAATAA | 286053 |
rs749033004 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166434 | ACCACACCTGGCTAA[-/T]TTTTATATTTTTAGT | 286053 |
rs749038566 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267332 | TTTCTAAATATATGT[C/T]CTCTTTATTGGTTTA | 286053 |
rs749043953 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207073 | TAAATAAAATTATTC[A/G]TACTTTTCATATTCA | 286053 |
rs749044265 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270664 | TTGAGATGGGAGGAT[C/T]GCTTGAGGCCGGCAA | 286053 |
rs749053918 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307206 | AGCTAGAGACAAGGA[A/C]ATTTTTTTTTCTTTA | 286053 |
rs749064735 | snp | A/C/G | 3.29789e-05 | 0.00406061 | missense, synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125366864 | GAACCATAACAAGAA[A/C/G]AGACATCGTCATTCC | 286053 |
rs749088618 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259939 | GCTGGAAACTGCATT[-/G]GGGCTCATGTAATCC | 286053 |
rs749103986 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190559 | AAAGATTAATTCAAA[C/T]TAAAGGATTGATTCC | 286053 |
rs749121029 | snp | G/T | 3.32817e-05 | 0.00407919 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366727 | AAGTTTCTGCTTAAG[G/T]CAGTAAAGGGGACTG | 286053 |
rs749149164 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113560 | TTCTGGGGGAGGAGA[C/T]TAAAGTGTACTAATA | 286053 |
rs749152512 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350818 | ATTTGGGTGGGGACA[C/T]AGCCAAACCATATTA | 286053 |
rs749171044 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352278 | CTGAGGTCAGTTCGC[A/G]ACCAGCCTGACCAAC | 286053 |
rs749202599 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208757 | CTTTGAAGAAGAGGT[A/G]GAATTTGAATAAGTG | 286053 |
rs749203443 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099707 | AGAGCAGTTGCAGTG[G/T]AGTGATAGAGATGGA | 286053 |
rs749206283 | snp | A/C | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128625 | ATCTTAACTGGGCTA[A/C]AAGCAAAGTGTGGCA | 286053 |
rs749214302 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275011 | GATGATAATAATAAT[A/G]ATAATAATAATAATA | 286053 |
rs749240397 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291337 | CTAAAAGGTTGCTGT[A/G]AAGAACTATATAAAA | 286053 |
rs749243938 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102409 | TCTGCTCTCTCCTCC[C/T]TGAAAAACTTCCAAG | 286053 |
rs749248704 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164353 | TCAAGGCTGTTTTCA[C/T]GACAGTTCTGTTTCA | 286053 |
rs749250606 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149627 | AAACAGTTTAAAAGC[A/C]CTTGTAACAACATTA | 286053 |
rs749254142 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143112 | CGCACACACACACAC[A/G]CACACACACAGAGGT | 286053 |
rs749255680 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122156 | ATGATTGACTTAGAA[-/G]GTTCTCTGGCTGAGC | 286053 |
rs749291740 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181724 | AAAAATGTTGAGCAT[A/G]AAGGATGGAATAACC | 286053 |
rs749295085 | in-del | -/TTATA | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089929 | TTCTATATATAAACT[-/TTATA]TTATATTAAATTTTT | 286053 |
rs749296122 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259352 | GAGCAGCCCACAAGC[A/G]AGCATTACCACCTGA | 286053 |
rs749310086 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116545 | TAGTTGCTTTTATAA[C/T]GTTAGAATTGGTTGC | 286053 |
rs749311675 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210700 | AGCCATCTCTTCCCC[A/C]GGTTGATTTCTTTAT | 286053 |
rs749315078 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243053 | ATGTGGAAAAAAAAT[C/T]ACCAGACATGGAAAT | 286053 |
rs749318407 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260747 | CTCATGCCTTAGCCT[C/G]CCGAGTAGCTGGGAT | 286053 |
rs749352742 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114093 | AACATAAATATTTTG[C/T]CCGGTATGTCTAGGC | 286053 |
rs749359880 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354828 | CTTTCCCTGCCCCTC[A/G]GTACAGCTTGAGCAT | 286053 |
rs749403392 | snp | A/G | 0.000141313 | 0.00840455 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155960 | AGAGATTACTGTCAT[A/G]TATATTTAGCAATTG | 286053 |
rs749404696 | snp | C/G | | | utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125367065 | CAACAGAAATGCAAT[C/G]ATATTGTTTATTTTT | 286053 |
rs749413028 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259502 | CATCCAGAAACCATC[A/G]TCGTGTCCTCCCTAC | 286053 |
rs749421807 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123504 | GAGCTAAAGCTCGAA[-/G]GGTTAAGTGACTTAT | 286053 |
rs749423968 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132250 | CTACAAGCGTACACC[A/C]TTGCACCTGGATAAT | 286053 |
rs749441867 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166299 | TTGAGACAGAGTCTC[A/G]CTCTGTCACCAGGCT | 286053 |
rs749449835 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355412 | TTAGAAAGCTACTGA[A/T]CTTTTGGCTGGGCCC | 286053 |
rs749465374 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166922 | TAGTCCTAGCTACTC[A/G]TGAGGCCAAGGCAGG | 286053 |
rs749466259 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342340 | GTCATGAAGGAGGAA[C/G]TTTGAAAAGTGTGAT | 286053 |
rs749479263 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117556 | TTATTTTATTTTTTT[A/G]AGAGATGGGGTCTTA | 286053 |
rs749481685 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197989 | ATGATTTGGGTCTCT[C/G]TCTGTTATTGGTGTA | 286053 |
rs749530372 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118730 | ACCAGAGAACTATAC[G/T]ACTATTAAGGTTAAA | 286053 |
rs749548273 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154751 | AGTGTTTTTAGAGCT[A/G]TAAGACAGTACACAG | 286053 |
rs749607165 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109069 | AAGTGAAAAAGAAAA[C/T]AACTTTGACTAAGGT | 286053 |
rs749611333 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134363 | ATGGCAAGTCTGAAA[A/G]TATGGGATCTATGTG | 286053 |
rs749637423 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346713 | AGTATTTCCAGTATT[G/T]ATTGGTTTGAAGTGG | 286053 |
rs749639983 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245236 | TGCAGTGAGCAGATA[G/T]TGCACCACTGCACTC | 286053 |
rs749651057 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202393 | TCATTTATTTAGTCA[C/T]CTATATATGTTGATA | 286053 |
rs749674739 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189263 | GGAAAAGCAGACATG[C/T]TTATCCCTTATGCAT | 286053 |
rs749692209 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238430 | TCAATAAATTATTAA[C/T]AGCAATCCCTTGCCA | 286053 |
rs749699285 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158841 | GGAAATAGACTGAAC[G/T]GGGACTGGGGAATGG | 286053 |
rs749717158 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190451 | TTGGAGAGAAGTGTA[A/G]CTACTCTCTCTCTTC | 286053 |
rs749719981 | in-del | -/CTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103589 | CTCTGCTCTCCTCTC[-/CTT]CTGTGTGACTCACAT | 286053 |
rs749729388 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219665 | ATTATTTTTCTTGGG[C/G]TTTCTGGAAAAGCTA | 286053 |
rs749734863 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332368 | GTAAGACCATGCTAA[C/T]AGTATTGTATGGTTT | 286053 |
rs749740736 | snp | A/T | 3.29598e-05 | 0.00405941 | missense | NSMCE2 | GRCh38.p7 | 8:125151229 | ATTTGCTACATTGGA[A/T]CGGCAACTAAACCAT | 286053 |
rs749764216 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273792 | TGCAGATTGGGGTCA[A/G]CAGGTGTCCTTCTTA | 286053 |
rs749782495 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305438 | CTGGAAGAGGAGAAA[C/T]GGAGTAGGGACAAGA | 286053 |
rs749825372 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318859 | GCAGATCCTTGTGAT[C/T]TCCCTGAATGGAGGA | 286053 |
rs749851454 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224300 | TTACTATGCAGAAGC[A/G]TTTTAGTTTGATGCA | 286053 |
rs749853135 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239502 | TAGTACCAGCCACTC[A/G]GGTGGTTGAGACATG | 286053 |
rs749862361 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217172 | CCTTTGATAGTTGTT[C/T]CCTAGGAGGCATGTG | 286053 |
rs749867652 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125197083 | TTTAAGTTCTTTGTA[A/G]ATTCTGGATATTAGC | 286053 |
rs749879589 | in-del | -/CTGT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266475 | CAAACACAATTAACA[-/CTGT]CTGTATTCACCTTCT | 286053 |
rs749897949 | in-del | -/AATA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115743 | ATAAAAAAAAATAAT[-/AATA]AATAAATAAATCTTT | 286053 |
rs749899045 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295377 | CAAAAGGGCCATTTG[A/T]TAATAAAATTAAAAA | 286053 |
rs749899392 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222382 | GAAAACTTTTGAAAT[C/G]TCCTCTAAGTAATTT | 286053 |
rs749901514 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212568 | TCAGGTACGTGTTCA[A/G]TACCAAACCGTTGGA | 286053 |
rs749915221 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103376 | TTTTATTTTACACAT[A/G]GAGCCAGAGGAGCAG | 286053 |
rs749951240 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154250 | AGAGCATTTGAATTT[A/G]TTATTTAAATAGACA | 286053 |
rs749956102 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347419 | CCTCCAGAGATACTT[C/T]TGTACTTTGTACAAA | 286053 |
rs749968036 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105068 | GCAGGGAGGAGGCCA[C/T]TGCAAGACTTTTCCC | 286053 |
rs749977593 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107573 | AATGATCTATTAGAG[G/T]GCAACAGTTTGGTGC | 286053 |
rs749980661 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233369 | AATTTTATGTTCTGG[G/T]TCTCATAAGAACAAA | 286053 |
rs749982954 | snp | A/G | 1.648e-05 | 0.0028705 | missense | NSMCE2 | GRCh38.p7 | 8:125366827 | ATCTTATCCAGGATG[A/G]AGCACTTAGAAGGGC | 286053 |
rs750005941 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351647 | TCTTTACTAAAGATT[-/A]AACTGATTTAATCCA | 286053 |
rs750046948 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140254 | GAAGAAGATTTGTAT[C/T]GGGAATATTGCAAAG | 286053 |
rs750054479 | in-del | -/TCT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279373 | CCTTATGAGAAATGA[-/TCT]TCTTATTTAAGAATG | 286053 |
rs750055130 | in-del | -/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298690 | ATTCATCTGTGGGTT[-/TT]TTTTTGTTTTTTTTT | 286053 |
rs750061679 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314591 | CATTGTGCTTGGCCG[A/G]GCCTTGCATTTTTAG | 286053 |
rs750069370 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186649 | AATGTGGGACCTAAG[C/T]GAGGAGAGTCAAAAC | 286053 |
rs750075771 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327542 | GTGTTTTTTTTTAAG[G/T]CTTTAATTTGAGCTA | 286053 |
rs750080546 | snp | A/G | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363078 | GGTTATGTTTTAAGG[A/G]AGGGTCATCCCAGCA | 286053 |
rs750085340 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155731 | CCTATAGTTCCAAAC[C/T]GTGGGCTTCAAATTG | 286053 |
rs750099993 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283620 | CCTCTGTGAATATCA[A/G]TAAGATCAGGATAAC | 286053 |
rs750100378 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125471 | ACTGGCACAGAACAT[G/T]AATAAGCAAGTGGAA | 286053 |
rs750112395 | snp | C/T | 1.65113e-05 | 0.00287322 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102510 | AAATTAAAACCTCTT[C/T]TGTGTCTACTTTGAG | 286053 |
rs750138147 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219777 | GACACTTTGGGCTTC[A/G]CTGATTGAAAACACC | 286053 |
rs750147835 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235055 | GTTCGAGACCAGCCT[G/T]GCCAACATGGTGAAA | 286053 |
rs750158770 | snp | A/T | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092836 | AAGAGAGATTGATTT[A/T]AACCAGTTATTCTCA | 286053 |
rs750159647 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288456 | TTTCAATTATTTTGC[C/T]TCTGAGCTATTTCTG | 286053 |
rs750162004 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241790 | GGAAATCACAGAATT[C/T]AGTAATTGAATTTAT | 286053 |
rs750170199 | snp | A/G | 3.32596e-05 | 0.00407783 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125182231 | TGTACAGTTTAAACA[A/G]CAGCTGAAAGAACTA | 286053 |
rs750171106 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273206 | CTATTAAAGACGCCA[A/G]TGAGACATTTTGGTA | 286053 |
rs750171897 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096862 | GTGATCAACTGCCTC[A/G]GCCTCCCAAAGTGCT | 286053 |
rs750174761 | in-del | -/GT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143086 | CCCAGGACACCCCCA[-/GT]GTGGGTGCACGCACA | 286053 |
rs750175380 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144756 | GTTTGTGCCTCATTC[A/G]TCATCTTCTATTCAT | 286053 |
rs750177614 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150120 | CCAGTTTTTCTGAAA[-/A]CAAGTTTGTTTTCTC | 286053 |
rs750177921 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151798 | TCACAGGAACAACAC[A/G]TAAGGCAGTTAAGGT | 286053 |
rs750185503 | snp | A/G | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367306 | GATCACTTGAGGTCA[A/G]GAGTTCAAGACCAGC | 286053 |
rs750216198 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239010 | TTCCTGATTATTTAG[A/T]TGCTGATTAACTAGT | 286053 |
rs750216628 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266855 | TACTCCAGTGTCTGT[C/T]AAAGAGGAAGAAGGA | 286053 |
rs750223308 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097915 | TTTTATTATATAGGC[A/G]GGAGGGAGTTAGGAC | 286053 |
rs750223814 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189840 | GGCACAAACATATAG[A/T]ATATACAGCAATACA | 286053 |
rs750227179 | snp | A/C/T | 0.000170659 | 0.00923591 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182094 | AGGTAATTTTGTTGT[A/C/T]TCCCTTAGGTGAAAG | 286053 |
rs750269747 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355220 | CAGTTCTATGGAACC[A/G]AAAGGTATGCCACAC | 286053 |
rs750297948 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354348 | ATTATCTTACCATAC[C/T]GGGAAATTTTTATGA | 286053 |
rs750311063 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211496 | AACCAGTCACCTGAT[A/G]GTGGGCTTAGTAGTT | 286053 |
rs750313503 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176474 | CTTTTTTTTGTTTCT[A/G]TTTATCCAGTCTCCT | 286053 |
rs750318312 | in-del | -/TTTTTA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315814 | TTTTTTTCCCTCTCT[-/TTTTTA]TTTTTAAAGTCAGGG | 286053 |
rs750331806 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177238 | CACAGCACTGAAGTG[G/T]GTGTTCCTGATTCCT | 286053 |
rs750351297 | in-del | -/ACAC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272805 | CATGTGTATATATAT[-/ACAC]ACACGTATATATATA | 286053 |
rs750366594 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358333 | GCTAGACTCTGTCTC[-/A]AAAAAAAAAAAAGGT | 286053 |
rs750371196 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131729 | GTATATTTTAAAAAT[A/G]CAAAATTGGAGCTTC | 286053 |
rs750372096 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261597 | AATATACTTACACTT[C/T]GAATTTTTTCTTGCC | 286053 |
rs750373076 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319679 | AGAAGACTAGTGAAC[C/T]GGACAACACAGCAGT | 286053 |
rs750373566 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096097 | CCTTGAGCTCCTTCC[A/G]TGCAGTAATTCTCTA | 286053 |
rs750376730 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306290 | AGCCATGATTGCCCC[A/G]CTGCACTCTAACCTG | 286053 |
rs750380010 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133294 | GTTTGTTTTAAAACA[A/G]ACATTTTTATGGAAT | 286053 |
rs750385338 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132852 | TAATTTGGCAATGTC[A/G]TATGAATGTAAAAGT | 286053 |
rs750390751 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341841 | ACCAACTTGAAGCCA[C/T]CAAGGACCCTTTAGG | 286053 |
rs750391546 | snp | A/G | | | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125130131 | TCCTGACAGTTTTGA[A/G]GAATCCTGCTTAGGT | 286053 |
rs750393106 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307502 | ACATCTCCTGAGCCC[A/G]TTTGTCTGGAGTGGC | 286053 |
rs750409523 | in-del | -/GTATTG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151099 | TGACTGATGTAGATT[-/GTATTG]ATGCAACTTTTTCCA | 286053 |
rs750414445 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125306383 | AAAACTGAGCAACAG[C/T]TGTTTTCACCACTCA | 286053 |
rs750442180 | in-del | -/A | 3.36112e-05 | 0.00409932 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151144 | TTTTAAATGGAAAAT[-/A]ATAATTGCAATTTTT | 286053 |
rs750459180 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135393 | TTTTTAATTTCTGTG[A/T]CATCCAGTTTACCAA | 286053 |
rs750470400 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100048 | CCTTATCTAGGAGCA[A/C]CAGTTTATTCATTTT | 286053 |
rs750471465 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229822 | ATGACTTATCATTTG[A/G]TAAATTTTTAAAATG | 286053 |
rs750481176 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150318 | TTATTCTAGATTTTG[C/T]CCTGGTTATTTCTTA | 286053 |
rs750482243 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193990 | GTTCTTGTGGAGAGT[A/G]TTGCCTCTTTGTATA | 286053 |
rs750493874 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310313 | TATTTAACCTTTTTT[C/G]CTCCTCAGTTTTTTT | 286053 |
rs750496256 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264780 | GAGTTTTCTTATACC[A/G]TCTTGCAGCCTCATT | 286053 |
rs750512172 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323100 | CCTATCGATGTATCT[C/G]ACTAAAGGTGTGCAA | 286053 |
rs750515224 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228547 | TGACATTTGAGCTGA[G/T]CCTTGAAGCATGGAT | 286053 |
rs750539285 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309431 | CTTTACCATAGAAGT[A/G]TTTTATTAAGATCAG | 286053 |
rs750546378 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216140 | TTCACCTATGTTGTA[G/T]CATGTATTACTATTT | 286053 |
rs750553317 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168769 | CACAGGCTTTCAGAC[G/T]ATAGGTATAGTTTGG | 286053 |
rs750569968 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180058 | CGCCTATAATCCTTT[C/T]CTAAGAACCAGCAAT | 286053 |
rs750620822 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147506 | AAGATATCAAGAGTG[-/T]TATGTGTTAAGGCAA | 286053 |
rs750629957 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230225 | TATCTTTACAAAAGG[C/T]TCATGCTTTTCAGTA | 286053 |
rs750633626 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310451 | GCCCAATCAATTGTA[A/G]CTATTGCAATTATGT | 286053 |
rs750643356 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298212 | TTGCAGTGAGCTGAG[A/G]TTGTGCCACTGCACT | 286053 |
rs750644115 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125157332 | TGGCATTCTACAGTG[A/G]TAGACAACTCTTAAC | 286053 |
rs750644500 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261176 | GTGGAATTGTTCAAA[A/G]TTTATTGTTTAACAC | 286053 |
rs750647638 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152122 | ATTATATAGTTAGAG[G/T]AAGCTTTTTTTAATG | 286053 |
rs750654292 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250677 | TTTTTAAGAGATGGA[A/C]TCTTGTTCTTTCACT | 286053 |
rs750690683 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169943 | TTTTTTTTTTTCATT[A/T]CCAAATAGCTGACTC | 286053 |
rs750705923 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329502 | TGAGGGTTAGGTGTT[C/T]ATGTTGATGTTTTAG | 286053 |
rs750709833 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302320 | GCACTGTTAAAAGCA[C/T]TGGGGATAAATCAGA | 286053 |
rs750720049 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348607 | CATGGGGGCGGTGTC[C/T]TCCCTACTTTTCTCA | 286053 |
rs750736473 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259146 | ACTCAGGTGATCCGC[C/G]CACTTCATGCTGGGA | 286053 |
rs750748286 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220625 | TCAGAAGGATCTGGT[A/G]AGTTAACATCATTAT | 286053 |
rs750778637 | snp | C/T | 1.65886e-05 | 0.00287993 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357672 | CTACTGGAAGTTGAT[C/T]ATTATCATTCCTGAA | 286053 |
rs750797355 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173242 | GGTGAAATCATTCTT[A/C]ACTTGGGTGCTGAGA | 286053 |
rs750820414 | in-del | -/AAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302640 | TTAATCAGATAGAAC[-/AAG]AAGATTAGAACAATG | 286053 |
rs750829356 | in-del | -/AC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125130654 | AAGCCCTTTCAGCAG[-/AC]AGAGCTAGGAAATAT | 286053 |
rs750861394 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116396 | TCAAAGATTTTCTTC[C/T]TTATGTTAAAAAAAT | 286053 |
rs750875496 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349751 | GGCTGTGTGTGGCCA[C/G]TACCAAATGTATTTT | 286053 |
rs750890619 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192706 | GTGGTATCACAAAAA[G/T]GGCACAATAATGGAA | 286053 |
rs750901250 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208264 | ATTCAGATATTAAAA[C/G]AACTTGAAAAGAGAG | 286053 |
rs750921901 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302991 | GGTAACGCAGTGTCC[A/G]TGCTGCAGCTCCACA | 286053 |
rs750927823 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205238 | AAGTGCATGTCTACA[A/G]TGTGAGACCTTTAAA | 286053 |
rs750933164 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289514 | TACTTATCAGAGGGC[A/T]TTCTTGTTATCAAAG | 286053 |
rs750936082 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099201 | AAATACAAGAATGTC[A/G]TTTGGCAATACCTGC | 286053 |
rs750938518 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173227 | ATTGTTGAGTCCCTT[-/G]GTGAAATCATTCTTC | 286053 |
rs750946046 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149089 | CAATTTTACCTGGAG[C/T]ATGACCTGAGCCTTT | 286053 |
rs750954873 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162195 | TGTTTTGAAAAGCTG[C/T]AGCAATACTTCTCAG | 286053 |
rs750977629 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141216 | ATAATCAAAGATGTC[A/G]TGGTCTCCATCACTC | 286053 |
rs750992687 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242387 | TTGACCTGAGCTTAC[A/G]TATGAGACACCACAT | 286053 |
rs750993446 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119569 | CAATCAGATTAAAAT[G/T]AGACTAGCACTTTAT | 286053 |
rs751005532 | in-del | -/AGTG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238163 | GGTCTCTCTTGAGAC[-/AGTG]AGAACTAAAGAAGAT | 286053 |
rs751020102 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235177 | ACCTGGGAGGCAGAG[C/G]TTGCAGTGAGCCAAG | 286053 |
rs751027126 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251562 | AGAGCTAGAAAATAG[A/G]TTTTTTTCAAAACCT | 286053 |
rs751034206 | snp | C/G | 1.73288e-05 | 0.00294348 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357852 | GGAAGTGGAGCCTTC[C/G]CTAGTGGTAGTTACT | 286053 |
rs751035410 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290678 | GTGTGGTCCAGGCAA[C/G]TGTGATCAAGGAGAC | 286053 |
rs751050469 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200564 | AGTCTGATGGGCTTC[C/G]CTTTGTGGGTAACCT | 286053 |
rs751065540 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249963 | AAACATTGGGAAACA[G/T]TATTTTATTATTTAT | 286053 |
rs751080131 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174708 | GCTCGAAGGAGGAAA[A/G]GTGTTTCCATGTTTG | 286053 |
rs751111215 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343590 | GCTACAGCAAGCCCA[C/G]ATTGTTCCATTGCAC | 286053 |
rs751111696 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314710 | TCCTGCCAGTAGCTT[G/T]CTTTCTTGATGTAAA | 286053 |
rs751115258 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220839 | TATATGATGAATGCA[A/G]GAAAAACTAACATTT | 286053 |
rs751127509 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094041 | ACTCCTGGCCTCAAG[C/G]AATCTTCCTGCCTTG | 286053 |
rs751129710 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341832 | GTGGGCAGAACCAAC[C/T]TGAAGCCACCAAGGA | 286053 |
rs751132288 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187088 | TAGCTCTAAAAGCTT[C/T]AGATTTAAGTTATTG | 286053 |
rs751156968 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193143 | TGCTTATGCTATTAA[A/G]AGTTAACAGGGTATA | 286053 |
rs751157618 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365537 | CCCATCTCAAAACCT[G/T]CCAGTGTTTTGTCTT | 286053 |
rs751175718 | in-del | -/AGAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350239 | CAAGAGTGATGTGAT[-/AGAG]AAAGTCTGTGTGGCT | 286053 |
rs751176383 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303138 | GTTCAGTTTCCTGTT[A/G]CTGACCACAGTAGAC | 286053 |
rs751196003 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270487 | AAAACAAAACAAGAC[A/G]AAAAACAGAATCTGA | 286053 |
rs751205261 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221589 | GTTGCGTATCACTTA[C/T]GTGAAATGCTTGAAA | 286053 |
rs751212041 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125127147 | TATCTCCTTTTCATG[A/G]TTCCTGGTTTGATGA | 286053 |
rs751224487 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142069 | ATGATTTTCACTTGC[C/T]ACCTTTTGGTTCCAA | 286053 |
rs751232492 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139516 | TGGGGAGGCCTCACA[A/G]TCATGGCAGAAGGCA | 286053 |
rs751236132 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221971 | ATAAAAAAGCTCATT[-/A]AAATCAGAATTTATA | 286053 |
rs751241441 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253293 | ATGTAGATTCTGAGC[C/T]TTTTTTGTGCTCAGC | 286053 |
rs751249200 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185091 | GGGATTACATTTGAC[-/A]AAAATCAGGATCTAA | 286053 |
rs751267149 | snp | A/G | 0.000115387 | 0.00759474 | synonymous-codon | NSMCE2 | GRCh38.p7 | 8:125366795 | TGGCTGTAGCCACAC[A/G]GATATAAGAAAGTCA | 286053 |
rs751290899 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336266 | TATTAAATAATCAAT[C/T]ACTCAATTAAATTCA | 286053 |
rs751297029 | in-del | -/AA/AAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312075 | AACTCCATCTCAATT[-/AA/AAA]AAAAAAAAAAAAAAA | 286053 |
rs751297789 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276944 | GATGACAGTGTGAAT[A/G]GCTCCCCCTGGAGTT | 286053 |
rs751299892 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261753 | AAAGAAGTAAAAAAA[A/C]AAAAACAAAAACAAA | 286053 |
rs751306229 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133527 | GGTGATTCACTTGAG[C/T]TCAGGAGTTCGAGAT | 286053 |
rs751331740 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289813 | TTCTGGTGTCTCCAG[A/T]TAGCAGTTGTTAATC | 286053 |
rs751339338 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355349 | AAAAGAGTAGAGAAG[A/G]GAAAGGGAAAGGAGA | 286053 |
rs751380031 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212766 | ACAGTTGCACAGTTT[A/G]TTATGTACTACATAA | 286053 |
rs751387876 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263018 | CCATTTCCTCCACTT[C/G]CTGTGCAGGCGACAG | 286053 |
rs751390555 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343103 | ATGTTTCATTAATAC[C/T]AAGATTCCAGGGCAT | 286053 |
rs751394095 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114684 | CAGTGAATGGGACAG[-/C]CCCTGCACAGCAAAG | 286053 |
rs751409510 | in-del | -/T/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266085 | GCGGGGCAGGTCAAA[-/T/TT]TTTTTTCTTTTTTTT | 286053 |
rs751440202 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178229 | TCAGGTCTCAGTTCT[A/G]TAACCTGGCCTCCAG | 286053 |
rs751452344 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155773 | TTTGGAGAGTGAACA[A/C]CAGTTTAGTTCAGGG | 286053 |
rs751480637 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133615 | GCATGGTGGCTCGCA[-/C]CTGTAATCCCCCCAG | 286053 |
rs751488246 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302420 | TTCCCATGGAATGAG[A/T]GAGGGAAAGGAAAGT | 286053 |
rs751490708 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248431 | ATCAGGCTAAGGCAG[A/G]CAGATCACTTGAGGT | 286053 |
rs751495482 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331179 | GTGGCAGGCGCCTGT[A/C]GTCCCAGCTACTCGG | 286053 |
rs751504535 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125118239 | TAGTCCCAGCTACTC[A/G]GGAGGCTAAGGTGGG | 286053 |
rs751506788 | in-del | -/ACTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126539 | TATTATAGCTTCAGC[-/ACTT]ACTTACTACCTCAAG | 286053 |
rs751520035 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295908 | CAATAATAACCGTTG[C/T]CCCTACTGAAGATCT | 286053 |
rs751529087 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158594 | TCCTAGCAGCTAATT[C/G]TTTGAATTACCCAAA | 286053 |
rs751541728 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344239 | TCCACCCTCATTGCC[A/G]TCAGTCCTACTTACC | 286053 |
rs751584934 | snp | C/T | 1.74345e-05 | 0.00295245 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182078 | TATTAACATTTAACT[C/T]AGGTAATTTTGTTGT | 286053 |
rs751591111 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122246 | TACAAAGATATGAAG[A/C]TACTTCAACAAATCT | 286053 |
rs751596846 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298429 | CTTGCCCAAAGTCAC[C/G]CAGCCAGTAAACGTG | 286053 |
rs751624985 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137937 | GGCACATAGTATGTG[C/T]TCAATAGATGTTTGC | 286053 |
rs751626301 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252550 | AGAAAAACCCTGTTT[C/T]ATCAGTATTAAGATT | 286053 |
rs751633709 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231768 | GGAATTTGGGAAAAC[A/G]CTTAACTGTAGCATG | 286053 |
rs751636768 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125128356 | TTGGACTAGAAAGGT[A/G]GTAAGGGATTGATGA | 286053 |
rs751648927 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346365 | ATGGACAGGCTATAC[A/G]AACAACTTGCATGTA | 286053 |
rs751670715 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125202092 | AGTATTTTGGCGAGA[A/G]TGTCCTGTTTTTCCA | 286053 |
rs751676513 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170011 | TACAGCCTGCTCTGA[C/T]ATCATCCCATCTCTG | 286053 |
rs751696383 | snp | A/C | 1.67536e-05 | 0.00289423 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357365 | AACACGATTCACTTC[A/C]CAGAGGCAGAAAGGT | 286053 |
rs751700650 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303331 | ACTGCAGTGCAGAAC[A/C]TGAAGAACAGACAGA | 286053 |
rs751720583 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125123574 | TATCTTCTGCAGTGC[C/T]AACCCACATGTGTAC | 286053 |
rs751740090 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347471 | CACAGGATATAAATA[C/T]TCATATCTGTCTCTC | 286053 |
rs751756361 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299538 | AACAGCATGGGGGAA[A/G]CAGCCCCCATGACCC | 286053 |
rs751765472 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238206 | AATGATTTCAACAAG[A/T]TTAAGGATAAGGATG | 286053 |
rs751769567 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109612 | TGCCCTGACATTTTC[C/G]TGTTGTTGTATTATT | 286053 |
rs751807386 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094998 | CTGGGGCTGCAGGCC[C/T]GCACCACCACATCCA | 286053 |
rs751808110 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259004 | GCCTCTTGGGTTCAA[A/G]CGATTCTCCTGCCTC | 286053 |
rs751809574 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211941 | GTTCTAGTTTCTGAT[A/C]TTCTGTTCCATTGGC | 286053 |
rs751820734 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291112 | AATATTAAGAAAGTT[A/G]AAAGGGGGAGAGGGG | 286053 |
rs751830332 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331775 | CAAATTTCAGTCAAC[A/G]GTAAAGTTTCAGCGT | 286053 |
rs751856586 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281588 | GTAATTACAGGAGTG[C/T]GCCATCACACCCAGC | 286053 |
rs751860389 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226141 | TGATCTTTTTCTTGG[C/T]ATATTAAACTGACAT | 286053 |
rs751860624 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242540 | GCTTAACAAAACTTG[A/G]TTCCAGCAAGAACTG | 286053 |
rs751882821 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114377 | ACTCAATAAATGAAA[G/T]AATGTGTTTAAAACC | 286053 |
rs751918272 | in-del | -/TTAACTCAGGTAATTTTGTTG | 1.75164e-05 | 0.00295937 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182071 | TATTATTATTAACAT[-/TTAACTCAGGTAATTTTGTTG]TTAACTCAGGTAATT | 286053 |
rs751929618 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194134 | ACAACAACTTAGTGT[A/G]GTAGGTAGATAGTAT | 286053 |
rs751937186 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208595 | GAGAGAAATATAAAC[C/T]GAGTGCTGTTGAATT | 286053 |
rs751955303 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364965 | CCAAAATTTGGTTCA[-/C]TTTGAGAACCAGATT | 286053 |
rs752004743 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283965 | GAGACCATCCTGGCT[A/G]ACATGGTGAAACCCC | 286053 |
rs752011501 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125145388 | ATTTTGTGGGGTGGC[A/G]GTGCGGGGGGGATAG | 286053 |
rs752020647 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336999 | ACATCTGATCCTCTT[G/T]CCTTTTTCAGTGACA | 286053 |
rs752033927 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125194838 | AATAAGTATGTAGTG[A/T]TATCTCATTGTGGTT | 286053 |
rs752036544 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199140 | TTTTCAAAAAACCTG[G/T]ATTCATTGATTTTTT | 286053 |
rs752038710 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340012 | TGTAGTTTTTTTTTG[-/T]TTTTTTTTTTTTTTT | 286053 |
rs752043703 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294706 | GGGGTTAGAATTATA[C/T]GTGAAAAAACATAAA | 286053 |
rs752105898 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323226 | GATGCCAATTCTCAC[C/T]GAATTGATCTGTTGA | 286053 |
rs752106072 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230157 | TTTGGAACATTCAGA[A/G]TTATCAAGCCTAAAC | 286053 |
rs752123967 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125310631 | ACCTGCAAGTACCTC[A/C]TCCATTCTTCCGTAA | 286053 |
rs752131191 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151763 | CCAGAAGCCAAACTT[A/G]TCTTTGTTGACTCCA | 286053 |
rs752133250 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113413 | GAAGCCCAGGAGTTC[A/G]AGGCTACAGCAAGAT | 286053 |
rs752135503 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137055 | TAAATTTTAAAGGAT[A/T]GATTTGCTATTATTT | 286053 |
rs752146714 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101256 | AATAATGGAGAAACT[A/G]CAATAGTAGTTCAGC | 286053 |
rs752147933 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221798 | TTGACTGCATTTTGA[C/T]TGCAACTAGGTGTGG | 286053 |
rs752155731 | in-del | -/TCTTTGTTTCAGAAATGAGGAAACAGAACCAGAGAGGTTCTAT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284433 | TGACCAACCCATTGG[lengthTooLong]CCTTATCGAGGATTG | 286053 |
rs752159165 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365786 | TGCTTGAACCCAGGA[A/G]GCGGAAGTTGCAGTG | 286053 |
rs752159552 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201998 | CAGTGAGCAAGGCTC[C/T]GTCGGCATGGGACCT | 286053 |
rs752184394 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271977 | AAGGCTATTTAGCCT[C/T]ACATTGACAACTGAA | 286053 |
rs752194426 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143667 | ACATGGCTTTGTAGA[A/T]TAAAAAACATCTGAT | 286053 |
rs752209719 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167853 | ACATGCTGTGATGTC[-/T]TTGAGGAGGTGAGGA | 286053 |
rs752212701 | snp | A/C | 1.64795e-05 | 0.00287045 | missense | NSMCE2 | GRCh38.p7 | 8:125366814 | ATAAGAAAGTCAGAT[A/C]TTATCCAGGATGAAG | 286053 |
rs752243246 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303354 | CAGACAGAATTCTTT[A/G]GAATTCTGATTCATT | 286053 |
rs752246000 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341479 | TAGGCTTTGAAAATG[C/T]GAAGCAAGATCAACC | 286053 |
rs752265161 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223349 | GGCAACAGAGCAAGA[A/C]CCTGTCCCAACAAAA | 286053 |
rs752273448 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296869 | ATCAGAGAATTTGCT[A/T]ATTTTTTTCTCTTAA | 286053 |
rs752283575 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259128 | GCTGGTCTTGAACTC[A/C]CGACTCAGGTGATCC | 286053 |
rs752286895 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114735 | CATTAGTGCTGAGGC[A/T]GAGAAACTCTGATAC | 286053 |
rs752312383 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366465 | GAATGGTGTGAACCC[A/G]GGAGGCGGAGCTTGC | 286053 |
rs752314059 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352147 | AGCACTGTAGCTGCT[A/G]TATAACATTCAGTAA | 286053 |
rs752320026 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338881 | TTCTGACATCTTAGC[A/G]TCTCAGTTTAGGCCA | 286053 |
rs752325581 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129546 | AAAGATTTGGCTCTG[-/TG]TGTGTGTGTGTGTGT | 286053 |
rs752331102 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304711 | AAAATACAAAAATTA[G/T]CCAGGCATGGTAGCA | 286053 |
rs752353315 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292859 | AGTTGCCCATCAAAG[C/T]TTATAATCATCTCCT | 286053 |
rs752355752 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170429 | TTAAGACAGAGTCTC[A/G]CTCTCTTGGCCTCTT | 286053 |
rs752360272 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210043 | AGTCACAGTTCATAG[C/T]TTAGACTCTAGATCC | 286053 |
rs752364095 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250796 | GCTGGGATAACAAGC[A/G]TGAGCCACCACACCC | 286053 |
rs752374067 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239608 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs752380320 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165745 | TGTTCTAATTTTTCT[A/G]TAATACAGCAGTTTT | 286053 |
rs752395877 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150685 | CCACGCCCGGCTGCT[A/G]TCTTTGATTGTTTTC | 286053 |
rs752406309 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133526 | AGGTGATTCACTTGA[C/G]CTCAGGAGTTCGAGA | 286053 |
rs752422887 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125119792 | TAAACCAACTTGATT[A/T]TTCTAGAGAAGATTA | 286053 |
rs752431295 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248754 | TCAAGTGTATTCTAT[A/G]TATTACCTCATGTAG | 286053 |
rs752432973 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244103 | GTGCCATAAAGCTAA[C/T]GATAAATGATTCCTC | 286053 |
rs752454118 | in-del | -/GAT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274995 | TCAGGACAATCTGAA[-/GAT]GATGATAATAATAAT | 286053 |
rs752483818 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219149 | TAATAATATACTCCA[A/C]ATATTTGCTATTTGG | 286053 |
rs752500173 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297081 | TTCACTGGGCCATTT[A/T]ACTGTGAGATATCCT | 286053 |
rs752507705 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329199 | AGTCCCCAGCAGCGG[A/G]CAATCCTTCCTTACC | 286053 |
rs752509599 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215995 | AGGTCTTGGCTGCAG[C/T]GAGCCATGATTGTGC | 286053 |
rs752511915 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201882 | CCGCTTTGTTTACCT[A/T]CTCAAGCCTTAGCAA | 286053 |
rs752521060 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250121 | CAGCCTCCCAAGTAG[C/G]TGGTACTACAGTCAT | 286053 |
rs752550586 | in-del | -/AGAA | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363526 | GGAAAGAGGAGAGAA[-/AGAA]AGAAAGAAAGAAAGA | 286053 |
rs752558691 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298090 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 286053 |
rs752579911 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168702 | CAGAGGCCTCACCTC[C/T]TAATACCATCACCTT | 286053 |
rs752597472 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216795 | TTCTTTTTGTAGACA[C/T]TTAAATACTGTTTAT | 286053 |
rs752597604 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316108 | CACTACACCTGGTCT[A/C]AACCTCATTCTTATC | 286053 |
rs752612274 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108149 | ACCCCCTGAAATGGC[A/T]CAGAAGACCACACTG | 286053 |
rs752619364 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155195 | AATAAAGCATTCAGG[C/G]AGAGTTAATAACCCA | 286053 |
rs752658914 | in-del | -/CAGGGTAAATACTAC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237759 | GTCTGCAAGGCTTAT[-/CAGGGTAAATACTAC]CTTGTGGCCATCTGT | 286053 |
rs752663621 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106790 | CACCTGAGTTCAGGA[A/G]TTGGAGACCAGCCTG | 286053 |
rs752672766 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156962 | TACCATTTTAGTTAA[A/G]CCAAATTTGGGAAGA | 286053 |
rs752681347 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301027 | GCTCAGTTATTTCTG[C/T]GTCACAATCATTAAC | 286053 |
rs752709549 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142233 | ATCTCATTTAGTCCT[C/T]ATATCAGCTTTCTGA | 286053 |
rs752717098 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094171 | AAACAGGAGAGCTAT[C/G]AATCTGACTGAAGCA | 286053 |
rs752728698 | in-del | -/T | 3.32077e-05 | 0.00407465 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151165 | TGCAATTTTTTTTTC[-/T]TTCAGCTGAAGTGAG | 286053 |
rs752738212 | snp | C/T | 1.6516e-05 | 0.00287362 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125151177 | TTCTTTCAGCTGAAG[C/T]GAGTAGTGAATATAG | 286053 |
rs752750958 | snp | C/T | 3.33222e-05 | 0.00408167 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182268 | CAATGTAAGTCAACA[C/T]GCTTTGCTTTGGTTC | 286053 |
rs752754506 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125114 | ATACAAGATCATGTC[A/G]TCTGTGAATGGAGAT | 286053 |
rs752756732 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109919 | TGTTACATTAGGAGA[C/T]TTTTTTTGAGATTAC | 286053 |
rs752758988 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254154 | TTCTCTTTTGACTCC[A/C]ATATTACATTTAATA | 286053 |
rs752773361 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332016 | CACAACATCCCTGCC[A/G]TGTAAGTAGCTGCTA | 286053 |
rs752779888 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204222 | ATAAAAGATAGGTCA[A/G]GGCCCTTTTTGCGAA | 286053 |
rs752792124 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191547 | GAGAGAATCTTTTTC[A/G]GTCACTTGCATTTAG | 286053 |
rs752794493 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203071 | AAATGAAATGGAGCT[A/G]CAGCTATCACTATGT | 286053 |
rs752826634 | in-del | -/TTTGT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253489 | TTGTTTTTATGTTTG[-/TTTGT]TTTGTTTTGTTTTGT | 286053 |
rs752840136 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333721 | GGTTTCACCATTTTA[C/G]CCGGGATGGTCTCGA | 286053 |
rs752840513 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359798 | TCTTCAAACTTGAGC[A/C]ACTATCAACATCCTC | 286053 |
rs752855342 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160227 | AGAGTTTCATTAAGG[A/T]TGAAAGTGATAGCAT | 286053 |
rs752896784 | snp | G/T | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125092548 | TGTGTTGTGTACATG[G/T]GCATGTGATAGGGAT | 286053 |
rs752900514 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098147 | GTCCCTTCCCAGACA[C/T]ACTGAATTAGAAATT | 286053 |
rs752913759 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334168 | TTTACTCAGAGTCTG[C/T]TCTTTAGACAACTGA | 286053 |
rs752933140 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280417 | TTCTATGGTTGCAAC[A/G]TCTGCTAAGCCTATT | 286053 |
rs752949084 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174181 | TTTGCAATAATCTGC[C/T]TGATTATTTGAATAT | 286053 |
rs752954735 | snp | C/G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111202 | TACTTCAGAGTTCAT[C/G/T]ATGAGTAAAAAACAA | 286053 |
rs752957798 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133782 | AACAAAAACCAAAAC[-/A]AAAAAAAAAGAAAAA | 286053 |
rs752990470 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245332 | GGACTTGCCACATTC[C/T]CTCACCATAATGCTG | 286053 |
rs753007613 | snp | A/T | 1.64741e-05 | 0.00286998 | synonymous-codon, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102456 | TATGGACACAGCTTC[A/T]AGTGTTGCTTTGGAT | 286053 |
rs753016267 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241077 | GGCACTATTCTTACG[A/G]GTTGAATATCCCTAA | 286053 |
rs753018029 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101380 | GCTAATTAATTGTGT[A/G]CTGTATGCTATACCA | 286053 |
rs753025647 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240753 | GCACTTAGCATATTC[C/T]TGTCTAATCAAGTAA | 286053 |
rs753030110 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189398 | GGTAAGTGCAACGAA[A/G]AACAAAGAAGGAGAG | 286053 |
rs753055784 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125152046 | TTTTACAAGATCAGT[C/G]ATTACTCAGTAGAAG | 286053 |
rs753062537 | snp | A/T | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125102392 | CCTTCAGTGGTGTAG[A/T]GTCTGCTCTCTCCTC | 286053 |
rs753062775 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359853 | ATAGGCATGGGAGAC[A/G]AGGACAGTTTTAAAG | 286053 |
rs753066031 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181743 | GATGGAATAACCACT[A/T]GTGAGTGTGAGAGAG | 286053 |
rs753066704 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232167 | GGAGTTCGAGGCTAG[C/T]CTGACCAACATGGAG | 286053 |
rs753070897 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102861 | TTGATTAACCAGTAG[A/G]TAGACTAAGCTTATG | 286053 |
rs753075296 | snp | G/T | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090469 | AGGGATCAAGAACAC[G/T]TGAAGATCAGTTTTC | 286053 |
rs753110612 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138253 | TTTAGAGACCTGGTC[A/G]ATCTCTGTCACTCAG | 286053 |
rs753116967 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267189 | ATTTTTGTATTTTTA[A/G]TAGAGACAGGGTTTC | 286053 |
rs753141425 | in-del | -/CT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110969 | CAGGAAAAGAAACCC[-/CT]GTTTGGCTAAGCAAC | 286053 |
rs753159432 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325501 | ACCACAAGCACATAC[C/T]ACCACACCTGGCTAA | 286053 |
rs753159701 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141949 | TGGGGGAGGGGTATG[C/G]TGTTTACAGTGCTTC | 286053 |
rs753169232 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225604 | GCCTCTCCAGGGAGA[C/T]TCCCAATAGCTTGTT | 286053 |
rs753188884 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183616 | TTTACCTTTTATCCA[C/T]GATATTTATTACTCA | 286053 |
rs753219903 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281152 | TCTTCCTTAAAACAC[A/G]TGAGAAAGTTATAGC | 286053 |
rs753236508 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347510 | CCCGATCTTATTCCT[C/G]TTTGTATCTATACCT | 286053 |
rs753239462 | snp | C/T | 1.67756e-05 | 0.00289612 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151146 | TTAAATGGAAAATAA[C/T]AATTGCAATTTTTTT | 286053 |
rs753251108 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326325 | CAATAGGAAATGATC[C/T]CCCAAATAAATTATT | 286053 |
rs753251182 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311816 | AGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 286053 |
rs753258087 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210163 | TGTCTGTTAAAATGA[C/T]ATAATAATAGTTTAC | 286053 |
rs753266560 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139684 | ATTCAATTACCTCCC[A/G]CTGGGTCTTTCACAT | 286053 |
rs753272123 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170098 | CATAGCATTTGTAGC[-/T]TGTAACCTAGTCCTC | 286053 |
rs753277151 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171341 | AATAGGCTCTAAGTA[A/C]ATAGTTGAAGTCTAG | 286053 |
rs753293609 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228979 | ACTATACCAGATTGA[A/G]GTAAGATGATAGCCT | 286053 |
rs753330650 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131481 | AGAGAATGAGGCAGA[C/T]CTCAAATATAAGGCC | 286053 |
rs753330656 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260341 | AATTAAAGATGAAAT[A/C]ATCTGAATAGCAGTT | 286053 |
rs753342102 | snp | C/T | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195489 | TAAGTCACTTAGTAA[C/T]TACCTAATGAATTAA | 286053 |
rs753364359 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341257 | TCACATGCCAGGCTG[G/T]AGATTATGCTAGTGA | 286053 |
rs753384406 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242133 | GAGAACCACTGTTAC[-/A]GGTGACAGTTGAAGC | 286053 |
rs753397654 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322347 | CACTGCAGTCTGAGA[C/G]TGAGTGAAGCAGAAA | 286053 |
rs753418294 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261555 | TTTTAATAAAACTCT[A/G]GTATCTTGAATTCTG | 286053 |
rs753423529 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166330 | GGAGTGCAGTGGCGC[A/G]ATCTCAGCTTACTGC | 286053 |
rs753424485 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292723 | ACAAACCACATGTGA[-/T]TCCCTGGTTCTGTCA | 286053 |
rs753432648 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245432 | AACACAAGTCAAAGG[C/T]TACGTCAAAACTATA | 286053 |
rs753436309 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113157 | TTCCTAGGACTGTGT[G/T]TATTCATTCATTTTA | 286053 |
rs753451926 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326466 | GTATATATAGTTTGT[A/G]TATATACACTGTGTG | 286053 |
rs753476166 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166513 | TTCAAGCGATCTCCC[C/G]GCTTTGGCCTCCCAA | 286053 |
rs753497098 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295111 | GCTGCAGAAAGGAAA[A/G]AACCTTTTTATAACT | 286053 |
rs753552502 | in-del | -/AAAAAAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327266 | GCAAGACTCCATCTC[-/AAAAAAA]AAAAAAAAAAAAAAG | 286053 |
rs753553250 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281208 | CACTGCAAACAACAG[A/C]ATGGGTTATTCATCT | 286053 |
rs753570364 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103072 | GGAGTTTGAGACCAG[C/G]CTGGCCAATATGGTG | 286053 |
rs753576490 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232255 | GTAATCGCAGCTACT[C/T]GGGAGGCTGAGGCAG | 286053 |
rs753577111 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299160 | CTACACATAATTTGT[A/C]TTTTTAAATCTGTAT | 286053 |
rs753592176 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269974 | ACTAAAGGACAAGCA[C/T]GGCCCTTATGGTTCT | 286053 |
rs753596320 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246409 | AGCTGCTCTCGATCT[C/G]CTGACCTTGTGATCC | 286053 |
rs753620027 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237046 | TAATATTCTTCTGTA[C/G]CTGGCACAGCAGTGA | 286053 |
rs753632040 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338482 | TTTGTCCTGACAGCA[C/G]AGTGCAAGCATCTAT | 286053 |
rs753633865 | snp | A/T | 0.000134345 | 0.00819479 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357196 | AGACCAGAGAGGCTT[A/T]TCAACTCTCCATTTT | 286053 |
rs753637937 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125237995 | ATTTTGCAAATTCCA[C/T]ACCTGTATGGATGAA | 286053 |
rs753651414 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125109497 | TTTTCCTTAGTTTTA[C/T]GAGATTGTTGACTTT | 286053 |
rs753652191 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189653 | CCTTTTCCTCTCAAT[A/T]CATCATCAGTAAGGA | 286053 |
rs753654373 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201978 | TTCTCAGGCTGCTGC[A/G]CTAGCAGTGAGCAAG | 286053 |
rs753659227 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252395 | AGCTGGATGTGGTGG[C/T]GGGTGCCTGTAGTCC | 286053 |
rs753669349 | in-del | -/AC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349013 | ATCTCAAAGCAAAAC[-/AC]ACACACACACACACA | 286053 |
rs753683775 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095370 | GAGTTGGGAGGATCA[C/T]TTGAGCTCAGGAGTT | 286053 |
rs753704507 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366064 | TCCCACGCTTCATTC[C/T]GGGTCCTGCCCTAGA | 286053 |
rs753713112 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317040 | CAGTCCACCTGCCTT[C/G]GCCTCCCAAAGTGCT | 286053 |
rs753718321 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158447 | GAAGAGGCAGGAGAC[A/G]CACAGGAGCAGCAGA | 286053 |