| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs3727 | snp | C/T | 0.0279526 | 0.114869 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521013 | ATACAGTACTTCTTT[C/T]GAAAAAATACACAAT | 56929 |
| rs166281 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | FEM1C | GRCh38.p7 | 5:115529745 | GAAAGAGATCTTAGA[A/C]CACGTTAACACCAAT | 56929 |
| rs256938 | snp | A/C | 0.460589 | 0.13473 | intron-variant | FEM1C | GRCh38.p7 | 5:115532640 | TTATAATCAGTATAT[A/C]TATAACTGTTTCCTG | 56929 |
| rs256939 | snp | C/T | 0.48435 | 0.0870631 | intron-variant | FEM1C | GRCh38.p7 | 5:115532541 | ATGCCTTTTTTTTTT[C/T]CCCTCTGTTTTCTAA | 56929 |
| rs256940 | snp | A/G | 0.383053 | 0.211653 | intron-variant | FEM1C | GRCh38.p7 | 5:115530494 | aaaaccagtaaggat[A/G]aagatttgaacatta | 56929 |
| rs256956 | snp | G/T | 0.491936 | 0.0629843 | intron-variant | FEM1C | GRCh38.p7 | 5:115541325 | TTTTCCAGAGGAAGT[G/T]TAAAAATCCCACAAA | 56929 |
| rs256957 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FEM1C | GRCh38.p7 | 5:115542223 | AAATTATACACAATC[A/G]AAAACCGGAGCCCTT | 56929 |
| rs256958 | snp | A/G | 0.21695 | 0.247806 | intron-variant | FEM1C | GRCh38.p7 | 5:115542368 | TGCTATATTTAATGC[A/G]TGTTCTTATAAAAGG | 56929 |
| rs256959 | snp | C/T | 0.495016 | 0.0496707 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545833 | ATTTGATGCTAAAAC[C/T]TACGTTGCATTAAAC | 56929 |
| rs372702 | snp | A/G | 0.45946 | 0.136478 | intron-variant | FEM1C | GRCh38.p7 | 5:115526911 | CCTTCTGGGAGTCTA[A/G]AATTTTGGGTATGAG | 56929 |
| rs813761 | snp | A/G | 0.486855 | 0.0799975 | intron-variant | FEM1C | GRCh38.p7 | 5:115536030 | aacttaagacagaaa[A/G]gagattactggttgc | 56929 |
| rs2161346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115538561 | TATGTAGTAGAATGC[A/G]GTTAGATGTCACAGT | 56929 |
| rs3776801 | snp | A/G | 0.173965 | 0.238157 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523956 | TGTGAATTTTATACA[A/G]TTGAAAGTCTTTTTT | 56929 |
| rs3776802 | snp | C/G | 0.172028 | 0.23753 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523909 | AAAGTAGAAACAGGG[C/G]GGAAACTTGAGAAGA | 56929 |
| rs3984997 | snp | C/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523129 | AAGTTATCTTTAAAG[C/G]TATACATAAGCTTGA | 56929 |
| rs3984998 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523133 | TATCTTTAAAGGTAT[A/G]CATAAGCTTGAAGAA | 56929 |
| rs5870659 | in-del | -/A | 0 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115529253 | GACATACAACACAGC[-/A]AAACTGCTGAAAACT | 56929 |
| rs5870660 | in-del | -/A/AA | 0.431916 | 0.171483 | intron-variant | FEM1C | GRCh38.p7 | 5:115535284 | TAAAAAAAAAAAAAA[-/A/AA]CAAACACAGAATGAG | 56929 |
| rs6868540 | snp | C/G | 0.0471551 | 0.14613 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545076 | CCTCTCGGATTTTCG[C/G]GGTGCTCCCTTAGGG | 56929 |
| rs6871805 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528077 | TCGAAAAAATACAAA[A/G]TATATTTATTTTGAA | 56929 |
| rs6878790 | snp | C/T | 0.482831 | 0.0910472 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546504 | GACCTGTCTCTCTCA[C/T]CTAATTCAATAAGAT | 56929 |
| rs6893854 | snp | A/T | 0.457737 | 0.139088 | intron-variant | FEM1C | GRCh38.p7 | 5:115530224 | atgccctttgcaaaa[A/T]ctaaatattaagaag | 56929 |
| rs6894123 | snp | A/G | 0.457271 | 0.139781 | intron-variant | FEM1C | GRCh38.p7 | 5:115530179 | atatgggtagaaaat[A/G]atctttagaagtgaa | 56929 |
| rs7712026 | snp | A/G | 0.18134 | 0.240387 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520610 | AATAATATATTTATG[A/G]TATACTTCTGATCAC | 56929 |
| rs7730778 | snp | A/C/G | 0.0170251 | 0.090679 | intron-variant | FEM1C | GRCh38.p7 | 5:115542197 | TGCTTTTAGTTTATT[A/C/G]CAATCAACAAAAATT | 56929 |
| rs7736971 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | FEM1C | GRCh38.p7 | 5:115528564 | AGATCATCTCATTAT[A/T]GATTTGAAATAATCC | 56929 |
| rs10043328 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115543820 | CCACACACCCCCCCC[A/C]CCCCCAAAGAAAAGG | 56929 |
| rs10053572 | snp | C/G | 0.452965 | 0.145963 | intron-variant | FEM1C | GRCh38.p7 | 5:115541847 | GCATGCTTGTACATA[C/G]ACAAGTATGCTTGTA | 56929 |
| rs10077232 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530041 | tttaatttaaacatt[A/T]aaaagacagaaactg | 56929 |
| rs11330098 | in-del | -/A | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521092 | GCAAAAAAAAAAAAA[-/A]GAAAAAGAAAAAAAG | 56929 |
| rs11960440 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | FEM1C | GRCh38.p7 | 5:115530616 | aaatactgaccatat[G/T]cttggccgtaaggca | 56929 |
| rs12110084 | snp | C/G/T | 0.0187777 | 0.0950591 | intron-variant | FEM1C | GRCh38.p7 | 5:115527351 | TATTGAATCTTTCCA[C/G/T]AAGTTTATCCTGTTT | 56929 |
| rs12110088 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | FEM1C | GRCh38.p7 | 5:115527515 | CTGACTATCGATGTT[A/C]ATTTGTTTAAAATAA | 56929 |
| rs12187973 | snp | G/T | 0.480853 | 0.0959518 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522740 | TCACAGGTAAACTGA[G/T]TTTTTCTCAAATCAA | 56929 |
| rs13162494 | snp | A/G | 0.0693013 | 0.172766 | intron-variant, missense | FEM1C | GRCh38.p7 | 5:115529571 | aggaagatgaGCCAC[A/G]TGGAAGCCTGGAGAT | 56929 |
| rs13177180 | snp | A/G | 0.455621 | 0.142197 | upstream-variant-2KB, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544896 | TAggcgcggggcggg[A/G]cgtcgcggccggggt | 56929 |
| rs13356084 | snp | C/G | 0.469247 | 0.120128 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544270 | TCACCCCCCACCCCC[C/G]GCCAAGGGATGATCC | 56929 |
| rs13357862 | snp | C/T | 0.454061 | 0.144427 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546756 | ACACATGCACGCACA[C/T]GCACACACACACAAA | 56929 |
| rs17137954 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | FEM1C | GRCh38.p7 | 5:115527583 | AAACACTCTTTTGTA[C/T]TAAGGACCTCTACTA | 56929 |
| rs17137960 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115537456 | GAGGATTCACAGTTC[A/C]AAATCCAATCTCCAG | 56929 |
| rs17137963 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115540133 | GGAAAAATCCTCTCT[G/T]GCTGCTAAATCACAT | 56929 |
| rs17472710 | snp | A/T | 0.102726 | 0.202016 | intron-variant | FEM1C | GRCh38.p7 | 5:115532223 | TAATGCTACTGCTTC[A/T]CAAATAAGTTCTTAC | 56929 |
| rs17852534 | snp | A/G/T | 0.000115638 | 0.00760302 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525025 | TAATAAGCTGCTGGC[A/G/T]GTCATTGGGCTTAAA | 56929 |
| rs33910606 | in-del | -/C | 0.499515 | 0.0155675 | intron-variant | FEM1C | GRCh38.p7 | 5:115543812 | ACTCCATCCCACACA[-/C]CCCCCCCACCCCCAA | 56929 |
| rs34179881 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521332 | CTTTTCCCATATAAC[C/T]TAAACAATTTTCCCA | 56929 |
| rs34470526 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534343 | ATGTTCAACTGTGAA[-/A]GCTTAGGTGCCTAGG | 56929 |
| rs34984849 | in-del | -/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522872 | TACCTGAATCTTTTT[-/T]AGTACTTTTCACTTA | 56929 |
| rs35045234 | in-del | -/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533031 | GTATGAATTTTATTG[-/G]CATGTAAATAAGTCA | 56929 |
| rs36043124 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540498 | ATACTGATACTGGGG[-/A]AAAAAATGACTTAGA | 56929 |
| rs55797760 | snp | C/T | 0.297382 | 0.245469 | intron-variant | FEM1C | GRCh38.p7 | 5:115542283 | TAGCCAACAAATCCA[C/T]ATCTGTTTAATCTAG | 56929 |
| rs55820160 | snp | A/C | 0.173643 | 0.238054 | intron-variant | FEM1C | GRCh38.p7 | 5:115539429 | GCTCTGAGAAGGACT[A/C]ACCTAATCACTACAG | 56929 |
| rs55825428 | snp | C/T | 0.336245 | 0.234652 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544366 | GCCCCCTCCCAATCT[C/T]CTCCATCGACCACAA | 56929 |
| rs56001355 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531217 | ATGAATAAATTATAT[C/T]TAATATAAAACCAAA | 56929 |
| rs56087439 | in-del | -/A | 0.488057 | 0.0763479 | intron-variant | FEM1C | GRCh38.p7 | 5:115542564 | CTCCAAGGTTGTTCT[-/A]AAAAAAAAAAAAACA | 56929 |
| rs56110877 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544916 | GCGGCCGGGGTGGGG[C/T]GACGGGGAGGGGGCG | 56929 |
| rs56212105 | snp | A/G | 0.237303 | 0.249677 | intron-variant | FEM1C | GRCh38.p7 | 5:115530624 | ACCATATTCTTGGCC[A/G]TAAGGCAAGTCTCAA | 56929 |
| rs57829926 | snp | C/T | 0.0158469 | 0.0875917 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545221 | GCACTCAGAGTTCCA[C/T]GTGGCTGGGGAGGCC | 56929 |
| rs57948082 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FEM1C | GRCh38.p7 | 5:115538629 | ACAAACAAGCAAACA[A/G]ACAAACCACTCCAGT | 56929 |
| rs58132177 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534860 | GTGATACCTACGCTG[C/T]TGGTCCTTGAGTAGC | 56929 |
| rs58762176 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FEM1C | GRCh38.p7 | 5:115527685 | TTTTCTCTATTCAGA[A/G]TAGCACAAAATCAAG | 56929 |
| rs58897289 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528002 | AAAAAAAAAAAAAAA[-/A]GGTAGCAAAAGCCAA | 56929 |
| rs60413296 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539778 | TGCTCTTTGTATATC[C/T]TAAGTCTAACAGCCT | 56929 |
| rs60640600 | snp | A/C | 0.173643 | 0.238054 | intron-variant | FEM1C | GRCh38.p7 | 5:115539430 | CTCTGAGAAGGACTC[A/C]CCTAATCACTACAGA | 56929 |
| rs62371181 | snp | C/T | 0.5 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115533275 | CTTTATTTTCTTTTA[C/T]GCCATGTCTATGTTT | 56929 |
| rs72817107 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524118 | TTCACAAACAATATA[C/T]TATATGGTATATTTA | 56929 |
| rs72817110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537354 | TGAAACGTAACTTCT[A/G]TCTTAAGCTCATGTT | 56929 |
| rs72817112 | snp | C/G | 0.0471551 | 0.14613 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545602 | GAAATTTCAGAAAAT[C/G]TGATTAGTTTTGGAG | 56929 |
| rs72817114 | snp | A/G | 0.0123036 | 0.0774623 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545823 | AACCTCTGGAATTTG[A/G]TGCTAAAACCTACGT | 56929 |
| rs73251202 | snp | A/C | 0.0174175 | 0.0916809 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522472 | ATTTACCTTTTCTTA[A/C]TGGTGAAATCAAATT | 56929 |
| rs73253004 | snp | A/C | 0.0170251 | 0.090679 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523802 | TAAAGCACTTATGGT[A/C]ACTGCAAATGGTAAC | 56929 |
| rs73253005 | snp | A/G | 0.15207 | 0.230021 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524464 | CTTCTCATCCAGCAA[A/G]TCACTAGCAGTTTGT | 56929 |
| rs73253008 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | FEM1C | GRCh38.p7 | 5:115535602 | GAAGAAGAAGAAGAA[C/G]AAGTGTTGGAGAGGG | 56929 |
| rs73253009 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | FEM1C | GRCh38.p7 | 5:115535645 | GGAACTCTTCTTACA[A/T]TGCTGACAGGAATGT | 56929 |
| rs73253014 | snp | A/C | 0.127944 | 0.218179 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546768 | ACACGCACACACACA[A/C]AAAAAATTAGTCAGG | 56929 |
| rs73780315 | snp | A/G | 0.124144 | 0.21601 | intron-variant | FEM1C | GRCh38.p7 | 5:115535051 | TCCTCTTTACTCTAA[A/G]TTTAACCATATGCCA | 56929 |
| rs73780316 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | FEM1C | GRCh38.p7 | 5:115537981 | TGGGGAATTAAATAA[A/G]ATTTTTCTTTAGCAT | 56929 |
| rs73780317 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FEM1C | GRCh38.p7 | 5:115540004 | ATGTACTGACATTTT[A/C]TTTCCTCAGAACCAT | 56929 |
| rs74327648 | snp | G/T | 0.021333 | 0.101051 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524216 | TGATATCAATCAAGC[G/T]AAATGAATGCTGGTG | 56929 |
| rs74395157 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FEM1C | GRCh38.p7 | 5:115530795 | AAGCCCAATGAAAAT[C/G]AGAAAATTTTTTTAA | 56929 |
| rs74621288 | snp | A/C | 0.120326 | 0.21374 | intron-variant | FEM1C | GRCh38.p7 | 5:115540778 | CTCCAATAACATAGG[A/C]TTTTAAAACATATCC | 56929 |
| rs74713184 | in-del | -/AA | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542576 | TCTAAAAAAAAAAAA[-/AA]CAAAACAAAAAGCTA | 56929 |
| rs74858537 | snp | C/T | 0.0310518 | 0.120672 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523530 | GATCTGTTTCCCAAA[C/T]TTAGCACACAATAAT | 56929 |
| rs74863613 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FEM1C | GRCh38.p7 | 5:115538273 | GCTAGCAATCCTTGC[C/T]ACATGCCTACATGAA | 56929 |
| rs74911277 | in-del | -/AA | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531536 | ATGATTCACTGTGCA[-/AA]TCTAACTCAGGGACT | 56929 |
| rs75167304 | snp | C/T | 0.0494327 | 0.149241 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520628 | TACTTCTGATCACAG[C/T]AAACCAATTAAAAAA | 56929 |
| rs75209410 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | FEM1C | GRCh38.p7 | 5:115536372 | CAGTCCTCATCTCTC[C/T]TTCTTCAGCCTACTA | 56929 |
| rs75422580 | snp | A/G | 0.02016 | 0.0983543 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545711 | TGTAAAGTCAATGAG[A/G]TCAGGTTCTTGAGCT | 56929 |
| rs75479409 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | FEM1C | GRCh38.p7 | 5:115526169 | CCTGGCCAGACTGCT[C/G]TTTAATATATCTAAG | 56929 |
| rs75650190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538862 | CCACAGATCCACATC[C/G]CAATAAACTTTCTGC | 56929 |
| rs75667088 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523554 | CAATAATTTCAGTGG[A/T]TTAGAGAAAGAAACC | 56929 |
| rs75771482 | snp | A/G | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544709 | CACGCCCCGCCACCC[A/G]AGCTGCCTCCCGCCC | 56929 |
| rs75900621 | snp | C/T | 0.103082 | 0.202275 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520778 | ACATAGAAGTATTAA[C/T]AATAAATGCTATCTT | 56929 |
| rs76214589 | snp | C/T | 0 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115526039 | TGGTCTTTTTTTTTT[C/T]CTTTAGAGACCAGGT | 56929 |
| rs76237597 | snp | C/T | 0.109814 | 0.206997 | intron-variant | FEM1C | GRCh38.p7 | 5:115537501 | ATGGATATTTCCCTA[C/T]TGGACTCAATTTGCA | 56929 |
| rs76370883 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | FEM1C | GRCh38.p7 | 5:115526639 | TGCCGACCTCTGGTA[C/T]TTACATACAATGTTT | 56929 |
| rs76559752 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522633 | TACCTAATGTGACTG[C/T]TTGCATTGATGACTC | 56929 |
| rs76722274 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FEM1C | GRCh38.p7 | 5:115537155 | TTCATCTGGGTCTCT[C/T]CCTATCTCTTCCACT | 56929 |
| rs76767872 | snp | A/G | 0.5 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115528001 | TGAGACTTCGTCTCA[A/G]AAAAAAAAAAAAAAA | 56929 |
| rs76942975 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115536617 | GCACTAGAAGAAGGA[A/T]TCTCTGCTTAGAATG | 56929 |
| rs76956480 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546856 | GGCTATAGTGAGCCA[C/T]GATCACACCACTGTG | 56929 |
| rs76964152 | snp | A/T | 0.0111196 | 0.0737302 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545916 | GATGAGAAAACAGAA[A/T]TTTTGAAAATGGACC | 56929 |
| rs77143128 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522314 | ATTTCAAGATACTGA[C/T]ATTTGATATTTCTAG | 56929 |
| rs77240345 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534286 | TTAATTTTAAAGACA[A/C]CTGTAATCTTTTAAT | 56929 |
| rs77247486 | snp | C/G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546094 | AAAAAATCACAACTT[C/G/T]ATTTTTGTATATTGT | 56929 |
| rs77367467 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523159 | AAGAAAGAAAGAACA[C/T]TGTTACTGACCTTTG | 56929 |
| rs77852843 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FEM1C | GRCh38.p7 | 5:115531886 | CCGGAGACATGGTCT[G/T]CATCTCCCACACACA | 56929 |
| rs77857886 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522127 | AAGCCCTCCCACCCA[A/G]CCCCCAAAGAGGAGG | 56929 |
| rs77915408 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527199 | AGTACAGTTATATGG[C/T]GAGTTACTTCCAAAT | 56929 |
| rs77922884 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | FEM1C | GRCh38.p7 | 5:115541969 | TTATTCAAATGTAAA[C/G]CAACAATGTAAACCA | 56929 |
| rs78150244 | snp | A/G | 0.084728 | 0.187577 | intron-variant | FEM1C | GRCh38.p7 | 5:115539883 | CAATAGCCTGTTAAA[A/G]AGTAATGAAAAGAGG | 56929 |
| rs78164791 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | FEM1C | GRCh38.p7 | 5:115531368 | AAAGCACTATCTGTG[C/T]GGAGAGAGCAATGAG | 56929 |
| rs78212163 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115538930 | AAAATTCAAAGCCCT[G/T]TTTAACTTCTACTTT | 56929 |
| rs78582211 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FEM1C | GRCh38.p7 | 5:115532735 | TACACAGATTCTACA[G/T]AATCCTTCTTAATGG | 56929 |
| rs78716330 | snp | A/C | 0 | 0 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521079 | GTGACACATAAGGGC[A/C]AAAAAAAAAAAAAGA | 56929 |
| rs79062172 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | FEM1C | GRCh38.p7 | 5:115535517 | CAACGTCATTAGCGA[C/T]TGGAGAAATATAAAT | 56929 |
| rs79199527 | snp | G/T | | | missense | FEM1C | GRCh38.p7 | 5:115525032 | CTGCTGGCGGTCATT[G/T]GGCTTAAAGGATCCA | 56929 |
| rs79206259 | snp | C/G | 0.02016 | 0.0983543 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546555 | TCTTCAAACTGAGCT[C/G]TGTATCCCTCATGGG | 56929 |
| rs79279851 | snp | C/T | 0.079617 | 0.182947 | intron-variant | FEM1C | GRCh38.p7 | 5:115540782 | AATAACATAGGCTTT[C/T]AAAACATATCCCAAT | 56929 |
| rs79558535 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FEM1C | GRCh38.p7 | 5:115530240 | CTAAATATTAAGAAG[C/T]TGTCTGATATTAAAA | 56929 |
| rs79577311 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | FEM1C | GRCh38.p7 | 5:115528699 | AATGCTTGGTATCCA[A/G]TCAAAAATAATGAAA | 56929 |
| rs79856776 | snp | C/T | 0.5 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115526040 | GGTCTTTTTTTTTTT[C/T]TTTAGAGACCAGGTC | 56929 |
| rs79860897 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115540301 | TTAATCTGCCCCCAA[C/T]ATTCATGAAGAATCA | 56929 |
| rs79949148 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546737 | ACTCCACACACACGC[A/C]CACACACATGCACGC | 56929 |
| rs80178268 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FEM1C | GRCh38.p7 | 5:115539647 | TCTAATAGAAGAAAG[C/T]ACTACTGTTGCACTT | 56929 |
| rs111415492 | snp | A/G | 0.5 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115540939 | AACATGGTTAGTTCA[A/G]CAGTAATTTGTTGTC | 56929 |
| rs111583986 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | FEM1C | GRCh38.p7 | 5:115530204 | AGTGAAAGTTTGGGA[A/G]AAAAATGCCCTTTGC | 56929 |
| rs111794209 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524143 | TATTTATATTAAATA[C/T]TGGGAAACCAATGTT | 56929 |
| rs112112169 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527676 | AGATGGCACTTTTCT[C/T]TATTCAGAGTAGCAC | 56929 |
| rs112495496 | snp | A/C | 0.5 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115526959 | ACATGACCAGCCCCC[A/C]GTAAAAACCTTGAGC | 56929 |
| rs112772052 | snp | G/T | 0.5 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115525803 | TATCTGATATTAAAC[G/T]TATTGAATAAATGAC | 56929 |
| rs112816676 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FEM1C | GRCh38.p7 | 5:115542891 | GTGCTTATAATGATG[C/T]ATCAAACTTCCTGAA | 56929 |
| rs112960438 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | FEM1C | GRCh38.p7 | 5:115543829 | CCCCCCACCCCCAAA[C/G]AAAAGGTGGTAAAGA | 56929 |
| rs112985826 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540752 | AACGGAAGTAATACC[A/C]GTTCTCATCTCTCCA | 56929 |
| rs113023710 | snp | A/G | 0.5 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115527635 | ATAGGCAATATAAGA[A/G]AAATCTGAATATAAA | 56929 |
| rs113344312 | snp | A/C | 0.084728 | 0.187577 | intron-variant | FEM1C | GRCh38.p7 | 5:115539542 | CTAAATATATCAAAG[A/C]TTTTCTCCCCTTTTG | 56929 |
| rs113379220 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FEM1C | GRCh38.p7 | 5:115529843 | ACTACTAAAATAATA[A/G]AGGGTATGCACATAA | 56929 |
| rs113763944 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | FEM1C | GRCh38.p7 | 5:115525677 | CAAAATATAATGTAA[C/T]ATATATATGCACTTT | 56929 |
| rs113814246 | in-del | -/CT | 0.5 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115539720 | CAATCAAACCATGAG[-/CT]CCTCAAGAGCAGGGA | 56929 |
| rs114167071 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | FEM1C | GRCh38.p7 | 5:115537983 | GGGAATTAAATAAGA[G/T]TTTTCTTTAGCATTT | 56929 |
| rs114373962 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | FEM1C | GRCh38.p7 | 5:115534211 | CTATGGTAAGTGCTC[A/G]TGCATTAAAGGGTGG | 56929 |
| rs114511614 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FEM1C | GRCh38.p7 | 5:115529042 | GAAAAGATGGAGACT[A/G]TAAGAGAAAGAGGGA | 56929 |
| rs114649496 | snp | A/C | 0.0310518 | 0.120672 | utr-variant-5-prime, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544637 | TGCTCCGCCTGCGGC[A/C]GCACAGCTCCTCCAT | 56929 |
| rs114789457 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115528345 | CCACAGTGGCCTCCA[A/C]CAATTCTGGAAGAGC | 56929 |
| rs114887040 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523435 | TGAAAGGTGGGTCAC[C/T]TTAAAAAGATTCTTC | 56929 |
| rs114919765 | snp | C/T | 0.0217236 | 0.101931 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523184 | CCTTTGATATTATGG[C/T]AGTAAATTGCATACT | 56929 |
| rs114955303 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543494 | TGTCTTTAGATCCAT[A/T]TATGTCCAGTTGAGA | 56929 |
| rs114980899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534777 | CTTCTCAAACTTTCA[C/T]GTATAAAATCACCAG | 56929 |
| rs114983196 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FEM1C | GRCh38.p7 | 5:115540037 | CCAGTGAATGACACA[C/T]AAAATGTCCTAAGGA | 56929 |
| rs115066776 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | FEM1C | GRCh38.p7 | 5:115534673 | GGACTGCAAAATATT[C/T]AACAAACACAGTAGA | 56929 |
| rs115082523 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115542235 | ATCAAAAACCGGAGC[C/T]CTTCTTCTGGACAAA | 56929 |
| rs115194484 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115531249 | CTCATAATAGAACTT[A/C]AACCAATCACATCAC | 56929 |
| rs115289236 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FEM1C | GRCh38.p7 | 5:115538608 | GTTAGATAAGTTTCT[C/T]TGAAAACAAACAAGC | 56929 |
| rs115407736 | snp | C/T | 0.0267878 | 0.112589 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546575 | TCCCTCATGGGATTG[C/T]TAAGGGATAGACGGA | 56929 |
| rs115854179 | snp | A/C | 0.0123036 | 0.0774623 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545740 | CTCTGAGTAATAAAT[A/C]GGGAACTAAAGCTTA | 56929 |
| rs116137739 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | FEM1C | GRCh38.p7 | 5:115526849 | GGTATCTCACTGTAC[C/G]TAAACTGTATGTAGA | 56929 |
| rs116175858 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544065 | CTTGCAACTGCAGGA[A/G]AGCTGGCCAAGGGCG | 56929 |
| rs116297996 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FEM1C | GRCh38.p7 | 5:115526594 | GTTTAATGATAAACA[C/T]TTTACTAATCGTCAA | 56929 |
| rs116518830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115529158 | AAGTCCAAGAATTTT[C/T]AGAAGCTGATGAAAG | 56929 |
| rs116701123 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115531614 | CTATAAGGTCTCTGT[A/T]GTAACCACTAAACTC | 56929 |
| rs116764222 | snp | C/T | 0.0138799 | 0.0821421 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546587 | TTGTTAAGGGATAGA[C/T]GGACACTTAGTTTAA | 56929 |
| rs117174094 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520596 | AAATTTGCATTCATA[A/G]TAATATATTTATGAT | 56929 |
| rs117293292 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115541210 | ATAACATTTATTAAG[C/T]TAAAAAACAGGTTAT | 56929 |
| rs117456018 | snp | A/G | 0.0123036 | 0.0774623 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546735 | CAACTCCACACACAC[A/G]CACACACACATGCAC | 56929 |
| rs117611256 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522763 | CAAATCAATAAGGAG[C/G]TTTTTATTGAGAACA | 56929 |
| rs117628490 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | FEM1C | GRCh38.p7 | 5:115528228 | AAACTGAAAAATTTA[A/T]TTTTAAAAATCTGCT | 56929 |
| rs118033702 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543595 | AACCAAAGTCCAATG[C/T]TAATTGCTGCACCCC | 56929 |
| rs137905967 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545884 | GTGTTTGGGAAATAA[C/T]GCCCATAATGAATCC | 56929 |
| rs137962013 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115534210 | ACTATGGTAAGTGCT[C/G]GTGCATTAAAGGGTG | 56929 |
| rs138090623 | snp | A/C | 1.80964e-05 | 0.00300797 | missense | FEM1C | GRCh38.p7 | 5:115524749 | ATGCAGCTTAAGAAA[A/C]CTGTATATAGTCTGC | 56929 |
| rs138341016 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523836 | TCCTTAAGGTTTGTA[C/T]AACCTAGTATGGGTC | 56929 |
| rs138382316 | in-del | -/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531683 | TTAATGGATATGGCT[-/G]GTTTCCCAACAAAAC | 56929 |
| rs138422563 | snp | C/T | 0.0174175 | 0.0916809 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545637 | TCAAACTGACTCTCT[C/T]TCTAAAGTAGCCTCT | 56929 |
| rs138504148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115539793 | CTAAGTCTAACAGCC[C/T]GGCACACTGCGGGAC | 56929 |
| rs138799892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527651 | AAATCTGAATATAAA[A/G]AAATGGCTTAGATGG | 56929 |
| rs138831562 | snp | A/G | 1.65616e-05 | 0.00287759 | missense | FEM1C | GRCh38.p7 | 5:115524942 | ATAAGATCATCAAAT[A/G]TAACAGTAGTACCCA | 56929 |
| rs138832944 | snp | C/T | 0.00914312 | 0.0669923 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522197 | TTATCCTCAAATTAT[C/T]GAGATCAACTAATGT | 56929 |
| rs139287818 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529609 | AAAACATCAACAAAA[A/G]GGGTAAATTTGTGAG | 56929 |
| rs139362179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540657 | TCAGGAGAAAATGCT[C/G]AAAAAATCTGAGCTA | 56929 |
| rs139430369 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115537549 | TTTATCCAACTAAGA[C/T]ACTAATTCTTCCCAA | 56929 |
| rs139480055 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FEM1C | GRCh38.p7 | 5:115535128 | CATGGAAAAGTTCCT[A/G]CATAGTAAATGGCAT | 56929 |
| rs139492029 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FEM1C | GRCh38.p7 | 5:115525876 | GAAATTCAAACTAAT[C/T]CATGGTCTCTTCGTA | 56929 |
| rs139575534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529830 | GCTATCTAGAATAAC[C/T]ACTAAAATAATAGAG | 56929 |
| rs139588472 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FEM1C | GRCh38.p7 | 5:115541760 | TGGAGTTGAATGACA[C/T]CCAAGGTTAGAAAAA | 56929 |
| rs139856245 | in-del | -/G/GG | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546399 | CCAAGAGGACTGGCT[-/G/GG]GTTTTATCCCCAGCA | 56929 |
| rs139901093 | in-del | -/A | 0.0205511 | 0.0992634 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545856 | CATTAAACTAGGATG[-/A]AAAAGTTTAAATGTG | 56929 |
| rs140001534 | snp | A/C/T | 9.89698e-05 | 0.00703393 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525286 | ATCATAAGCCATTAT[A/C/T]AGTGTCTGTGGCACT | 56929 |
| rs140337712 | snp | A/G | 6.72291e-05 | 0.00579742 | missense | FEM1C | GRCh38.p7 | 5:115524585 | GGACTGTTGTCATCC[A/G]AGTCTCTGACGTTCA | 56929 |
| rs140342926 | snp | A/G | 0.000232577 | 0.0107812 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525579 | TCTTCATGATGTCCA[A/G]ACTTCCAGATTCTGC | 56929 |
| rs140484229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528095 | TATTTATTTTGAATA[C/T]ACCCACATACCAGGA | 56929 |
| rs140554114 | in-del | -/CCACACACACGC | 0.208169 | 0.246476 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546724 | GGTGAAATCCCAACT[-/CCACACACACGC]CCACACACACGCACA | 56929 |
| rs140616688 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115531944 | TTATTCCATCCTAAG[A/T]ACTTCTCCCAGCACC | 56929 |
| rs140887361 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FEM1C | GRCh38.p7 | 5:115526582 | TATTTTAGCTAAGTT[C/T]AATGATAAACATTTT | 56929 |
| rs140951976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538879 | AATAAACTTTCTGCA[C/G]ATCTAAACCCCAACC | 56929 |
| rs141027164 | snp | A/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545492 | TTACCCTCACACACG[A/T]GAAGTCTCTCGGACT | 56929 |
| rs141134064 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FEM1C | GRCh38.p7 | 5:115540193 | ATTGGTTCCTGCTTT[C/T]GTTACCATTAACCCA | 56929 |
| rs141292170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527520 | TATCGATGTTCATTT[A/G]TTTAAAATAATTTCA | 56929 |
| rs141299251 | snp | A/C | 0.0115144 | 0.0749975 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521426 | TAACTTCAAATTCAT[A/C]ATGGGCACCAAATTA | 56929 |
| rs141435838 | snp | A/G | 0.0138799 | 0.0821421 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520696 | AACAAAAGTCTCCCC[A/G]TATCTTTAGCTTCTG | 56929 |
| rs141861349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115539562 | CTCCCCTTTTGGAAT[C/G]CCATGGGAAAAGAAG | 56929 |
| rs141933892 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524950 | ATCAAATGTAACAGT[A/G]GTACCCAGCAGGCCT | 56929 |
| rs141946137 | snp | C/G | 1.64988e-05 | 0.00287213 | missense | FEM1C | GRCh38.p7 | 5:115525164 | GAGGTATCAGGATGA[C/G]AAGGACCAAGAATAC | 56929 |
| rs142240969 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FEM1C | GRCh38.p7 | 5:115530595 | AGGGATACAGGGAGC[A/G]TATCCAAATACTGAC | 56929 |
| rs142649288 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546572 | GTATCCCTCATGGGA[C/T]TGTTAAGGGATAGAC | 56929 |
| rs142713039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115541493 | CTTTCTGAAAGGCAG[A/G]CACTATCACAACTGC | 56929 |
| rs142744025 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115529649 | ATAAATACTGATTTT[A/T]AAAATAATATCTTGT | 56929 |
| rs142892732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115538844 | AAAACTGCCAAAACC[C/T]TTCCACAGATCCACA | 56929 |
| rs143093254 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115540061 | CTAAGGAATTATTCT[A/G]ATTTAACTCTAGTCT | 56929 |
| rs143139481 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521209 | GTAAAAGAGTATGTC[A/G]TTATCTCATCCAGCC | 56929 |
| rs143173360 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | FEM1C | GRCh38.p7 | 5:115533595 | ATGCCAAGTACTATA[C/G]ATTTAGCTCAAGAAT | 56929 |
| rs143411451 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532979 | TAATAAATGCGTAGT[A/G]TATGTTTGTCAAAAA | 56929 |
| rs143665793 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528290 | TATGCAGGAGAAGAA[A/C]AAACTAGAGAGGTCA | 56929 |
| rs143873933 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | FEM1C | GRCh38.p7 | 5:115530506 | GATGAAGATTTGAAC[A/C]TTACAAACTTGATTT | 56929 |
| rs143932079 | in-del | -/A | 0.102726 | 0.202016 | intron-variant | FEM1C | GRCh38.p7 | 5:115530823 | TAACTGGGTGATCAT[-/A]AAAAGCACTAAATAA | 56929 |
| rs144077365 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | FEM1C | GRCh38.p7 | 5:115537910 | TCTATCTGAATACCA[A/G]CAGTTTTTAGTTTAC | 56929 |
| rs144110303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115531289 | CAAAAAACTTTCACA[A/G]TTTCTCTAAGGAAAA | 56929 |
| rs144190437 | snp | C/G | 0.000545576 | 0.0165073 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543404 | GATCAAGGAGGAAAC[C/G]TCCTCTTTGGATTTG | 56929 |
| rs144332148 | snp | C/T | 1.65625e-05 | 0.00287766 | missense | FEM1C | GRCh38.p7 | 5:115524477 | AAGTCACTAGCAGTT[C/T]GTTTGTGCAAGTTTG | 56929 |
| rs144343811 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524115 | TAATTCACAAACAAT[A/G]TATTATATGGTATAT | 56929 |
| rs144356594 | snp | C/T | 3.52684e-05 | 0.00419916 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524638 | TATTGCAGTAACTTG[C/T]AGAGATGGAAATTTA | 56929 |
| rs144572598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542693 | GTAACTCTGGGGAAC[C/G]CATTTCCCAAGAATT | 56929 |
| rs144957300 | snp | C/T | 1.6495e-05 | 0.0028718 | missense | FEM1C | GRCh38.p7 | 5:115525332 | TTAGTCCTATCACTG[C/T]ACCTCATGTTCATTG | 56929 |
| rs144981737 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521652 | ACTTACACATTAACT[C/G]CAGTCAATAACACCG | 56929 |
| rs145006222 | snp | A/G | 0.000116031 | 0.00761592 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524908 | CTCTATTTCAAGGAC[A/G]CTTTTGCAAAGTATG | 56929 |
| rs145051921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115525985 | TACTGACAAGTCACT[G/T]AACTTCCAGGTCAGT | 56929 |
| rs145071838 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115527555 | AACATGACTACTACA[C/G/T]CAAGTATATTTTAAA | 56929 |
| rs145220644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115532808 | CATAAACATTTCCCC[A/G]TTGATGGACATCTGC | 56929 |
| rs145233271 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115542391 | ATAAAAGGATTATCT[A/G]TTGACCACAAACAAA | 56929 |
| rs145241186 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545803 | TCTTCATATAGTAGT[C/T]GATAAACCTCTGGAA | 56929 |
| rs145311016 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FEM1C | GRCh38.p7 | 5:115533143 | CTACCAATGGGATTA[C/T]AAAAATTGTTTAAAG | 56929 |
| rs145696037 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543980 | CTTTGTTCTAGTTTT[C/G]CTTTGCACACGCCCA | 56929 |
| rs145996986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541590 | AAGCGTGAAAAGACA[C/T]ATTTTTGTTCAAGAA | 56929 |
| rs146263635 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FEM1C | GRCh38.p7 | 5:115536759 | CCTCCCTTCATTAAT[C/T]CTTTGTATAAGGCAC | 56929 |
| rs146346732 | snp | C/T | 6.61146e-05 | 0.00574917 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524995 | TAGCATAAAGGAGAA[C/T]AGTTCTGCAAAAGAT | 56929 |
| rs146408045 | in-del | -/TAAC | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532643 | TAATCAGTATATATA[-/TAAC]TGTTTCCTGCTTTTC | 56929 |
| rs146487783 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538445 | GGAGCTTATAATCTT[C/T]CCTCTCTTAAATCCA | 56929 |
| rs146807012 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | FEM1C | GRCh38.p7 | 5:115531840 | GGCTGGATTTGAACC[A/C]TGGGCCATAGTTTGC | 56929 |
| rs147020932 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115520970 | ATATGATTTTCCATT[A/G]TGTGACAATTTATTA | 56929 |
| rs147087036 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FEM1C | GRCh38.p7 | 5:115539637 | TTTCCAAATATCTAA[C/T]AGAAGAAAGTACTAC | 56929 |
| rs147090462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115533788 | GAATCTGAGATGAAA[C/T]TAAGGATATGCAGCA | 56929 |
| rs147350117 | snp | A/C/G | 0.00311874 | 0.039366 | missense, synonymous-codon | FEM1C | GRCh38.p7 | 5:115524700 | TCTTGTCCACAGCCA[A/C/G]ATGAAGAGGGCTGAA | 56929 |
| rs147529913 | snp | C/T | 0.000214555 | 0.0103553 | missense | FEM1C | GRCh38.p7 | 5:115525440 | TTAATACGTTCTGTC[C/T]TGCTGGTCTGTGCAT | 56929 |
| rs147553193 | snp | C/T | 1.65389e-05 | 0.00287562 | missense | FEM1C | GRCh38.p7 | 5:115524445 | TTAAATTTTTAGCTA[C/T]TTCCTTCTCATCCAG | 56929 |
| rs147796545 | snp | C/T | 0.000503744 | 0.0158625 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524584 | GGGACTGTTGTCATC[C/T]GAGTCTCTGACGTTC | 56929 |
| rs147848857 | in-del | -/TA | 0.173965 | 0.238157 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521761 | TAACACAAATTTAAG[-/TA]TTTTATTATAATCCA | 56929 |
| rs147888948 | snp | A/C | 3.29712e-05 | 0.00406011 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543349 | GGTGCCCATACCTGG[A/C]GGCCATCAAGAGTGG | 56929 |
| rs147945978 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115539215 | CTACAGCGTTTTCTA[C/T]TGGTCTGTAGTACTG | 56929 |
| rs148102497 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521297 | GGTTTCTGTTGGGCA[A/G]TATGATTTTTAAAGA | 56929 |
| rs148102531 | snp | C/T | 9.90001e-05 | 0.00703493 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525094 | CCATAGGTTGATGCA[C/T]CGTTTGAAATTTCCA | 56929 |
| rs148156655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115528527 | AATAGACTAGCTATC[A/G]CAAAAACTTAAATCG | 56929 |
| rs148379759 | in-del | -/TTCTC | 0.0178098 | 0.0926698 | intron-variant | FEM1C | GRCh38.p7 | 5:115527672 | GCTTAGATGGCACTT[-/TTCTC]TATTCAGAGTAGCAC | 56929 |
| rs148689516 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115530584 | ATTTTGCCCCCAGGG[A/G]TACAGGGAGCATATC | 56929 |
| rs148746141 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | FEM1C | GRCh38.p7 | 5:115542630 | CATATTCCCAAGTAG[A/C]TTAAGCATAAGCCTA | 56929 |
| rs148852051 | snp | A/T | 0.0130921 | 0.0798413 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545728 | CAGGTTCTTGAGCTC[A/T]GAGTAATAAATCGGG | 56929 |
| rs149078223 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521160 | CTAACTCTAAAATGG[C/T]TAAAGTTCTAGGCAA | 56929 |
| rs149105245 | snp | C/G | 1.69381e-05 | 0.00291011 | missense | FEM1C | GRCh38.p7 | 5:115524840 | AAAATAATAGAAAGG[C/G]CCTTATTTAACTGTA | 56929 |
| rs149216093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115532973 | TACCTTTAATAAATG[C/T]GTAGTATATGTTTGT | 56929 |
| rs149317521 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115536197 | CATTGAATTGTATAC[A/C]CTTTAAGTGGTTTTG | 56929 |
| rs149606295 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523886 | TAGAAATGGTTAGGA[C/G]AAACAATAAAGTAGA | 56929 |
| rs149706495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115526681 | CAACAGTCAGTCATT[C/T]TAGGCATGTCTGTAG | 56929 |
| rs149785479 | in-del | -/C | 0.0126979 | 0.078662 | intron-variant | FEM1C | GRCh38.p7 | 5:115527596 | TATTAAGGACCTCTA[-/C]TATTCCCCATGTTTT | 56929 |
| rs149867472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529954 | GGCAGGACAAATAAA[A/T]ATCAGAAAAGTACCC | 56929 |
| rs150004013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541906 | ATAAAAAACTGTAAA[C/T]AGTGGTTGTCAGCGC | 56929 |
| rs150248691 | snp | C/G | 0.0248432 | 0.108648 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545576 | ACCTCAGAACACACA[C/G]GGAGGAAACTGAAAT | 56929 |
| rs150314818 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | FEM1C | GRCh38.p7 | 5:115532290 | TTTCTTATATCCCAG[-/A]AGCAACTAGCAACCT | 56929 |
| rs150339884 | snp | A/C | 0.000153988 | 0.00877328 | missense | FEM1C | GRCh38.p7 | 5:115524673 | CAGGGTACCGCCCTA[A/C]ACATGTAGTATTCTT | 56929 |
| rs150506568 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FEM1C | GRCh38.p7 | 5:115535105 | CAATTAGATTACAAA[A/G]TTTCATCCATGGAAA | 56929 |
| rs150659799 | snp | G/T | 0.000131989 | 0.00812264 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525186 | CAAGAATACGTTCTC[G/T]GATTAATAGTGCCTG | 56929 |
| rs150666542 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FEM1C | GRCh38.p7 | 5:115529030 | GGTAAAAGAACAGAA[A/G]AGATGGAGACTATAA | 56929 |
| rs150913161 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523293 | AACTAAAAGTGATTT[A/G]CAGTTCAATTACTGA | 56929 |
| rs151000895 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115526101 | CCTGGGCTCAAGCAA[C/T]GCTCCTGCCTTAGTC | 56929 |
| rs151073202 | in-del | -/A | 0.0310518 | 0.120672 | intron-variant | FEM1C | GRCh38.p7 | 5:115525756 | TGGTTTACAAACGAG[-/A]AAAAAAAAATTCCCC | 56929 |
| rs151190954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530829 | GGTGATCATAAAAAG[C/T]ACTAAATAATAAATT | 56929 |
| rs180829616 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115531432 | CAGTAAAGTTTAATA[C/G/T]TGGATATTCAAGGAT | 56929 |
| rs180835069 | snp | A/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522557 | AACCAAAAAGTCTAA[A/T]GTTCTCTTGTTTATT | 56929 |
| rs180866405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115541914 | CTGTAAATAGTGGTT[A/G]TCAGCGCATTAGAGA | 56929 |
| rs180963282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115537310 | AATGAACCAGTGAAG[A/G]AACTACATTGTACCC | 56929 |
| rs180984418 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545311 | ATCAGAGCCAAGGAA[A/G]AAGGGAAACCCCATA | 56929 |
| rs181022801 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526883 | AATGCAGTTTATGCT[A/G]AATGTCTGGTTTCCT | 56929 |
| rs181052508 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545861 | AACTAGGATGAAAAA[A/G]TTTAAATGTGTTTGG | 56929 |
| rs181061614 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115527717 | ATAAAATGTAGCAAA[A/C]GCTGGCCAGGCGCGG | 56929 |
| rs181147072 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536522 | CCAAGTATTTTATTC[C/T]CTGAATAACTAACAG | 56929 |
| rs181513317 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546429 | ATATGTCACAGTTCT[A/G]TACTCTCCCAGGGTA | 56929 |
| rs181632509 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FEM1C | GRCh38.p7 | 5:115532642 | ATAATCAGTATATAT[A/G]TAACTGTTTCCTGCT | 56929 |
| rs181806042 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115541252 | TAAAACTGCATACAT[A/G]TATCAGTATGCAAAA | 56929 |
| rs181818416 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521911 | TTTCAAAACCTCCCA[A/G]TGGCATTTGTGGAGA | 56929 |
| rs181839407 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536848 | AACGCTAAAAAATAT[C/G]TGCATCCAAAGAGGT | 56929 |
| rs181945699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115533697 | ATCTCCACATCATGT[C/T]TTCTTTTCGCATTCT | 56929 |
| rs182250984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534199 | AAGGTCAGGAAACTA[C/T]GGTAAGTGCTCGTGC | 56929 |
| rs182251841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115539584 | GAAAAGAAGAAAACC[A/G]TTGTCCCCTCAGGTT | 56929 |
| rs182496554 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115530434 | AAGCAAACAAATCTG[C/T]AAACATTAGTACATC | 56929 |
| rs182514893 | snp | A/G | 8.24926e-05 | 0.0064218 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525127 | GTCTGCATAGACAGC[A/G]CCTCTATATCTAATA | 56929 |
| rs182758751 | snp | C/G | 8.77955e-05 | 0.00662496 | intron-variant | FEM1C | GRCh38.p7 | 5:115542926 | AGTGGTAGACATTTA[C/G]AAAAACAAAGAAGCT | 56929 |
| rs182796826 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537421 | GATCTACTCATTCTC[A/T]CCAAACTGCTCAATT | 56929 |
| rs182845761 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520629 | ACTTCTGATCACAGC[A/T]AACCAATTAAAAAAC | 56929 |
| rs182862026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115528207 | CCCTCCCACTAACAA[C/T]TAAAAAAACTGAAAA | 56929 |
| rs182935907 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115529371 | GAACAACAGAAACTA[A/G]GAGACAGTAAATGAT | 56929 |
| rs182970295 | snp | A/C | 0.00398564 | 0.0444627 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523374 | TAAGCAAATTCTCTA[A/C]ACCTAATCACACCAT | 56929 |
| rs183067706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542521 | TAGAACAAACAAGAC[C/T]ATGACTCAATAAATA | 56929 |
| rs183076023 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524154 | AATATTGGGAAACCA[A/G]TGTTGTAAATTTGAT | 56929 |
| rs183531845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542083 | TTTGCTGTCGTATAA[A/G]TAGATTCGTGTAAGG | 56929 |
| rs183562953 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115536315 | GAAGCAGCAATTAGA[C/G]GGTCTTTTATTATAA | 56929 |
| rs183601168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538404 | TCCCTACAGAAAGGC[C/G]TATAAAACATAGTGC | 56929 |
| rs183675051 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115520969 | CATATGATTTTCCAT[C/T]GTGTGACAATTTATT | 56929 |
| rs183743088 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534696 | ACAGTAGATTCTGCC[A/G]TTTGTAAATTCCTCA | 56929 |
| rs184136967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115532035 | GCACTTCCTTCTTTA[A/C]CATTTTAACTTCTTG | 56929 |
| rs184441767 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540629 | AATCAAGTTAAATAC[C/T]GTTCACAGCTTCTCA | 56929 |
| rs184450041 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521865 | AGAAAATAAAATCAG[A/G]GACAATTTTGAGCTA | 56929 |
| rs184520516 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FEM1C | GRCh38.p7 | 5:115531101 | TACAAATAGAAAAGA[G/T]AATTTAGTGGGAAAA | 56929 |
| rs184577064 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543635 | ACACAACCACGAAGA[A/G]TATGTTCCGTCCTAC | 56929 |
| rs184589702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115525753 | TACTTGGTTTACAAA[C/T]GAGAAAAAAAAATTC | 56929 |
| rs184958389 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FEM1C | GRCh38.p7 | 5:115539926 | TTCAAATATCAACCG[C/T]CTGTTTAAAAGTAAT | 56929 |
| rs185077528 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521480 | TCAGATTTATGAATA[A/G]GAAAAATGACTATTT | 56929 |
| rs185085170 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545112 | TTCGGTCCCATCTCA[C/G]AGACCCCAGAAGGGA | 56929 |
| rs185095034 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115526313 | CCCCAAAAAGCTCTC[A/C/G]TAAGAAAAACAAATC | 56929 |
| rs185097843 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530759 | TTTTTAATACTCACT[C/T]GCTTCGTCGGTCAAA | 56929 |
| rs185186443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537332 | ATTGTACCCGAAGGC[A/C]AGTAAGTGAAACGTA | 56929 |
| rs185322245 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FEM1C | GRCh38.p7 | 5:115536556 | TAGGTTGATGGAGGA[A/G]GTAAGAAGGGATAAA | 56929 |
| rs185331158 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115541422 | ATAAAAGATCACACA[A/G]TCTACAGCAAATATG | 56929 |
| rs185734277 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FEM1C | GRCh38.p7 | 5:115542222 | AAAATTATACACAAT[C/T]AAAAACCGGAGCCCT | 56929 |
| rs185736515 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523817 | AACTGCAAATGGTAA[C/T]GAGTCCTTAAGGTTT | 56929 |
| rs185751561 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115535622 | GTTGGAGAGGGTGTG[A/C/G]AGAAACTGGAACTCT | 56929 |
| rs185852030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527145 | CTCATAATTCAGCTG[C/T]ATGTCCTTATGACAT | 56929 |
| rs185872853 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545978 | CACATAATTCCTTAG[C/T]ACCACTAGGAGAAAT | 56929 |
| rs185888978 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FEM1C | GRCh38.p7 | 5:115527726 | AGCAAAAGCTGGCCA[A/G]GCGCGGTAGCTCACG | 56929 |
| rs185976923 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545625 | TTTTGGAGGCTGTCA[A/T]ACTGACTCTCTTTCT | 56929 |
| rs186096410 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FEM1C | GRCh38.p7 | 5:115533784 | CCAGGAATCTGAGAT[G/T]AAATTAAGGATATGC | 56929 |
| rs186489708 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FEM1C | GRCh38.p7 | 5:115539590 | AAGAAAACCATTGTC[C/T]CCTCAGGTTATAAGT | 56929 |
| rs186497353 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FEM1C | GRCh38.p7 | 5:115542034 | ATGCTACTTTTAAAT[A/T]TTAATGGCTTTTAAA | 56929 |
| rs186552363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537773 | AAGTAGGTGTGCTGA[C/G]GTAACCAACAGCTGA | 56929 |
| rs186634945 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FEM1C | GRCh38.p7 | 5:115533212 | TTTTTAATTTATATT[A/G]CCTCTATTCCTTGGT | 56929 |
| rs186717530 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523231 | CCTAGATGCCTAGAT[A/C]TGGCTTGGCAAGCAT | 56929 |
| rs187136994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530544 | ATAAATAAAAGAACA[C/T]GGCACTCAACAACCA | 56929 |
| rs187293723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534354 | GTGAAGCTTAGGTGC[C/G]TAGGAATAGAATCAA | 56929 |
| rs187348515 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546615 | TAAAGGCTACCAATT[G/T]CTGCTGTGGCTCACA | 56929 |
| rs187374258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537008 | AAAAAACTCATCTAA[C/T]GACAGAAAACTTCAA | 56929 |
| rs187481478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529588 | GGAAGCCTGGAGATA[C/T]AGGCAAAAACATCAA | 56929 |
| rs187614420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528761 | TGGAAATAAAGAGCT[G/T]ACAGAAAAGCCCAAC | 56929 |
| rs187724755 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521066 | AACTAGTTGTTTAGT[A/G]ACACATAAGGGCAAA | 56929 |
| rs187729417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115536191 | AAAAGCCATTGAATT[A/G]TATACACTTTAAGTG | 56929 |
| rs187746279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542537 | ATGACTCAATAAATA[C/T]AGTAATTTCTACTCC | 56929 |
| rs187876153 | snp | G/T | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520737 | TAGAAAAAAAATTTA[G/T]AATAAACTGTACATA | 56929 |
| rs187973292 | snp | A/C/T | 0.00716266 | 0.059414 | intron-variant | FEM1C | GRCh38.p7 | 5:115531149 | CAACTGCCAATTCAG[A/C/T]GTACTACTCATTTCT | 56929 |
| rs188084095 | snp | C/T | 4.97047e-05 | 0.00498496 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543417 | ACCTCCTCTTTGGAT[C/T]TGCTTGCCAACAATT | 56929 |
| rs188219004 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115535183 | TTCCTAACAATTTTC[A/T]TGTTTAAGTAAGACA | 56929 |
| rs188373737 | snp | C/G | 0.00377278 | 0.0432684 | intron-variant | FEM1C | GRCh38.p7 | 5:115525640 | AGAGAGAGAAAAAAA[C/G]AAATAACATACATTG | 56929 |
| rs188633893 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FEM1C | GRCh38.p7 | 5:115536460 | GAGGTGGTCCACTTG[C/T]AAGATGAGGATAGGG | 56929 |
| rs188766600 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524188 | TATAATGCTTTAGCC[A/C]ATGAGAGCACAATGA | 56929 |
| rs188893310 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544421 | GGCCTCCAGCCCGCT[G/T]CCCGCCTTCGGCTCC | 56929 |
| rs188907633 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FEM1C | GRCh38.p7 | 5:115525821 | TTGAATAAATGACAT[A/G]ACCAAATTAGGTGTA | 56929 |
| rs189152933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530877 | TATTTTTTAAATAGC[C/T]AAGTTTCCATCTAAA | 56929 |
| rs189262987 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522196 | GTTATCCTCAAATTA[C/T]CGAGATCAACTAATG | 56929 |
| rs189371624 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FEM1C | GRCh38.p7 | 5:115541744 | AGGTAGCTATGTGTG[C/T]TGGAGTTGAATGACA | 56929 |
| rs189533278 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521523 | TCCATTTGTCTTTAT[A/G]AAGTAGACTGGCATC | 56929 |
| rs189542406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540795 | TTTAAAACATATCCC[A/G]ATTTGACTTAAATAT | 56929 |
| rs189545884 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521900 | ATTAACTGGTTTTTC[A/G]AAACCTCCCAATGGC | 56929 |
| rs189647578 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545702 | TAAGAGCAATGTAAA[A/G]TCAATGAGGTCAGGT | 56929 |
| rs189797930 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115539995 | CCAAGCACAATGTAC[C/T]GACATTTTCTTTCCT | 56929 |
| rs189802440 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FEM1C | GRCh38.p7 | 5:115536608 | ATCAAAGGAGCACTA[C/G]AAGAAGGATTCTCTG | 56929 |
| rs189918644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527255 | ACATAGCATGTGTAC[A/C]AGAAAGTATTTTAAA | 56929 |
| rs190023238 | snp | A/T | 0.031825 | 0.122064 | intron-variant | FEM1C | GRCh38.p7 | 5:115533955 | CATAAAAAAAAAAAA[A/T]TTCATGATTTCTCAA | 56929 |
| rs190149468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534432 | AAGAACTAGTTAGAG[C/G]CCTAAGAATTATCTG | 56929 |
| rs190278005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529965 | TAAAAATCAGAAAAG[G/T]ACCCAGGAGATGAAA | 56929 |
| rs190288630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537400 | ATGAACAGCAGTAGT[A/G]CTCAGGATCTACTCA | 56929 |
| rs190337620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115526385 | TAAAAGGAGATATCT[C/G]AAGTGTCCTTTCATA | 56929 |
| rs190575960 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545202 | AAAGATAAAAAGATT[C/T]AATGCACTCAGAGTT | 56929 |
| rs190682598 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546130 | TGTTCAGAAGTTTAT[A/G]TAGTTTTGCATAATT | 56929 |
| rs190688595 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | FEM1C | GRCh38.p7 | 5:115527926 | GAATCACTTGAACCT[C/G]GGAGGTGGAGGTTGC | 56929 |
| rs190925443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542520 | CTAGAACAAACAAGA[A/C]CATGACTCAATAAAT | 56929 |
| rs190935051 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524061 | AATGAATAAGCCTTT[C/G]GCAGACAATTTTAGA | 56929 |
| rs190962614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537090 | CTTCCCAAAGGGAGG[A/G]AAAAAAGAAGGAAGA | 56929 |
| rs191101915 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523301 | GTGATTTGCAGTTCA[A/G]TTACTGAGTATTTCA | 56929 |
| rs191336611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542042 | TTTAAATTTTAATGG[A/C]TTTTAAAAATTAGGT | 56929 |
| rs191418567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115536232 | TTTTATCTCAATAAG[G/T]CTGTTTTAAAAATCC | 56929 |
| rs191681924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115525685 | AATGTAATATATATA[C/T]GCACTTTAGAACCTA | 56929 |
| rs191753179 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FEM1C | GRCh38.p7 | 5:115538270 | AATGCTAGCAATCCT[C/T]GCCACATGCCTACAT | 56929 |
| rs191895893 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115529214 | TACAAACTCCAAGAA[C/G]GACAAATAAAAAGAA | 56929 |
| rs192187260 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546734 | CCAACTCCACACACA[C/T]GCACACACACATGCA | 56929 |
| rs192305766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530675 | TCACTGAGTATGTTC[C/T]AAGTCCACTTATGAA | 56929 |
| rs192358141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115533689 | GATTTTCCATCTCCA[C/T]ATCATGTCTTCTTTT | 56929 |
| rs192396082 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520842 | GTTTTTCTGAAACAG[C/G]AGTTTACTATCATTT | 56929 |
| rs192521990 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115526257 | ATTGCCAAGTTGAAT[G/T]TCAACTGTCTTAGCC | 56929 |
| rs192716165 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521211 | AAAAGAGTATGTCAT[C/T]ATCTCATCCAGCCTG | 56929 |
| rs192852871 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543630 | CGGATACACAACCAC[A/G]AAGAGTATGTTCCGT | 56929 |
| rs192918255 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FEM1C | GRCh38.p7 | 5:115539924 | TGTTCAAATATCAAC[C/T]GCCTGTTTAAAAGTA | 56929 |
| rs192965452 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115540513 | AAAAAAATGACTTAG[A/C]ATAAGTTTGGCCAAA | 56929 |
| rs193038859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115530927 | GTAAATTAAATTAGA[A/G]AAAGTAGAAGCAAAC | 56929 |
| rs193188232 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521700 | TAGTTAGACTCAAGA[C/G]TGTAATTGGTTCATT | 56929 |
| rs193259356 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FEM1C | GRCh38.p7 | 5:115535295 | AAGTTAAAAAAAAAA[A/C]AAACAAACACAGAAT | 56929 |
| rs199515754 | snp | A/G | 0.00199802 | 0.0315439 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543358 | ACCTGGCGGCCATCA[A/G]GAGTGGCGTGGCCCC | 56929 |
| rs199624849 | in-del | -/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539429 | GCTCTGAGAAGGACT[-/C]ACCTAATCACTACAG | 56929 |
| rs199678597 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531131 | ACATAAACTCCTGTC[C/T]CCCAACTGCCAATTC | 56929 |
| rs199819294 | snp | A/G | 0.000508643 | 0.0159393 | missense | FEM1C | GRCh38.p7 | 5:115524816 | TTCTCTAACAAGCAA[A/G]TTAAGTGCAAAATAA | 56929 |
| rs200520465 | in-del | -/ATATT | 0.0260105 | 0.111035 | intron-variant | FEM1C | GRCh38.p7 | 5:115533863 | GAGAAAAAGAAAAAC[-/ATATT]ATATTAAACAATTCT | 56929 |
| rs200831453 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115543820 | CCACACACCCCCCCC[-/A]CCCCCAAAGAAAAGG | 56929 |
| rs200916953 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542047 | ATTTTAATGGCTTTT[A/T]AAAATTAGGTAGTGA | 56929 |
| rs201013763 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522997 | AGTGAGAGAAAGAAA[C/T]GAAGAAAGAGAAAAG | 56929 |
| rs201100876 | snp | C/T | 5.21934e-05 | 0.00510823 | missense | FEM1C | GRCh38.p7 | 5:115524623 | ACCACATTCTATCAG[C/T]ATTGCAGTAACTTGT | 56929 |
| rs201126135 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543119 | TTCCAAATGGCCATC[A/G]AAACACGCAGCTCGA | 56929 |
| rs201184590 | in-del | -/GTGA | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522929 | GGCATTAGCAAATCT[-/GTGA]GTGAGTGAGTGAGAG | 56929 |
| rs201406557 | in-del | -/CAAA | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538623 | CTGAAAACAAACAAG[-/CAAA]CAAACAAACCACTCC | 56929 |
| rs201655348 | snp | A/T | 0.000348881 | 0.013203 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524365 | ATGCCCTTTATAATA[A/T]ATTCTATGATTCACT | 56929 |
| rs201684493 | in-del | -/A | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521092 | CAAAAAAAAAAAAAA[-/A]GAAAAAGAAAAAAAG | 56929 |
| rs201883849 | snp | A/G | 0.000527652 | 0.0162342 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543314 | ACTGCATTGCTCTAG[A/G]AGGAATTCCACCATG | 56929 |
| rs202030585 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520601 | TGCATTCATAATAAT[A/G]TATTTATGATATACT | 56929 |
| rs202173828 | in-del | -/G | 0.0785177 | 0.181917 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544973 | TGCGTGCAACGCGCT[-/G]GGGGGGCGGGGCGCT | 56929 |
| rs202175210 | snp | G/T | 0.000424678 | 0.0145657 | intron-variant | FEM1C | GRCh38.p7 | 5:115525654 | AGAAATAACATACAT[G/T]GAGGGACCAAAATAT | 56929 |
| rs207466347 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528917 | TAGAACTGAAAAACT[C/T]GGTGAGTGGCTTTAA | 56929 |
| rs207466348 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538263 | CCCTTTTAATGCTAG[C/G]AATCCTTGCCACATG | 56929 |
| rs367602859 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526664 | ATGTTTACATAAAAT[G/T]TCAACAGTCAGTCAT | 56929 |
| rs367977295 | snp | A/G | 7.55986e-05 | 0.00614765 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524275 | AACTGTTACCAATTC[A/G]TGCTTTAACAGTGCT | 56929 |
| rs367999662 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FEM1C | GRCh38.p7 | 5:115529661 | TTTAAAAATAATATC[C/T]TGTAGGGCTTGAAAT | 56929 |
| rs368046443 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537358 | ACGTAACTTCTATCT[C/T]AAGCTCATGTTACTG | 56929 |
| rs368104656 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543140 | CGCAGCTCGAAGAGG[A/G]GTTGAATTGGTTAAA | 56929 |
| rs368112992 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545885 | TGTTTGGGAAATAAC[A/G]CCCATAATGAATCCT | 56929 |
| rs368139137 | snp | A/G | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520560 | TTTTACAAATGAAAA[A/G]TGATGGAAAACAAAC | 56929 |
| rs368223708 | snp | C/T | 0.000212427 | 0.0103038 | intron-variant | FEM1C | GRCh38.p7 | 5:115542903 | ATGTATCAAACTTCC[C/T]GAAAATAAGTGGTAG | 56929 |
| rs368462835 | snp | A/G | 0.00016594 | 0.00910727 | intron-variant | FEM1C | GRCh38.p7 | 5:115525643 | GAGAGAAAAAAAGAA[A/G]TAACATACATTGAGG | 56929 |
| rs368512797 | snp | G/T | | | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544080 | GAGCTGGCCAAGGGC[G/T]CCAGGCTGGAAGGCC | 56929 |
| rs368718109 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529063 | GAAAGAGGGAACAAC[A/G]TCAGAATATTGTTAA | 56929 |
| rs368831061 | snp | C/T | 3.34046e-05 | 0.00408671 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524335 | GGAAACAAAAGTCTC[C/T]AGCTTTTCTGGGATA | 56929 |
| rs368946028 | in-del | -/G | 0.0205511 | 0.0992634 | intron-variant | FEM1C | GRCh38.p7 | 5:115535882 | ATGGAATATTATTCT[-/G]CAATAAAAAGAAAAG | 56929 |
| rs369239412 | snp | A/G | 3.54629e-05 | 0.00421072 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524291 | TGCTTTAACAGTGCT[A/G]AAATACAGTCAAGTT | 56929 |
| rs369935915 | snp | A/G | 3.39784e-05 | 0.00412165 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524596 | ATCCGAGTCTCTGAC[A/G]TTCACATCAGCACCA | 56929 |
| rs370152871 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527942 | GGAGGTGGAGGTTGC[A/G]GTAAGCAGAGATCAT | 56929 |
| rs370195584 | in-del | -/CA | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546758 | ACATGCACGCACACG[-/CA]CACACACACAAAAAA | 56929 |
| rs370292868 | snp | A/G | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520569 | TGAAAAGTGATGGAA[A/G]ACAAACGTATAAAAT | 56929 |
| rs370633109 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526811 | TTCTCTATACTGATC[C/T]AAAACTTTCCCTAAA | 56929 |
| rs370880624 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546751 | CACACACACATGCAC[A/G]CACACGCACACACAC | 56929 |
| rs371134496 | snp | C/T | | | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544095 | GCCAGGCTGGAAGGC[C/T]TGAGGCCGGGTTTCG | 56929 |
| rs371195487 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546770 | ACGCACACACACACA[A/C]AAAATTAGTCAGGCA | 56929 |
| rs371210908 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530972 | ATTAATGAAAAAAGG[A/G]ATACGTATGCGAATA | 56929 |
| rs371214945 | snp | C/T | 1.64955e-05 | 0.00287184 | missense | FEM1C | GRCh38.p7 | 5:115525258 | CTTCTGCACTGTTCA[C/T]TTCCTTGGCATAATC | 56929 |
| rs371237757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534226 | GTGCATTAAAGGGTG[G/T]TAGTATTCCTCAAGA | 56929 |
| rs371258411 | snp | C/T | 0.000313814 | 0.0125223 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543270 | GTTTCGCCATCAAAA[C/T]TGACGGAGCCCCCAA | 56929 |
| rs371309920 | snp | A/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546324 | GTAATTGCCACTGAG[A/T]AGAAAATATAAAAGA | 56929 |
| rs371559891 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541684 | AGACTAGATAAATTA[C/T]GTACATTCATACAAT | 56929 |
| rs371702693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540221 | CCATAGAAAAAAATC[A/C]AGAACCAATGAGAGA | 56929 |
| rs371843337 | snp | C/T | 0.00210015 | 0.0323368 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524279 | GTTACCAATTCGTGC[C/T]TTAACAGTGCTAAAA | 56929 |
| rs372057405 | snp | A/C | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522441 | CAAAAAGTTGGAGAT[A/C]GTTCATTTATATCCA | 56929 |
| rs372149129 | snp | C/T | 1.65411e-05 | 0.00287581 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543407 | CAAGGAGGAAACCTC[C/T]TCTTTGGATTTGCTT | 56929 |
| rs372166759 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538762 | CTAATATGCCTACTT[G/T]CCAATTCCTGGACCC | 56929 |
| rs372192640 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530128 | GAAGATACAAAGAAA[A/G]CTCAAGACACACTGC | 56929 |
| rs372388464 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529419 | AAAAGTAACTGCCAA[C/T]TTAGAAAAAATTCTA | 56929 |
| rs372520461 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537313 | GAACCAGTGAAGGAA[C/T]TACATTGTACCCGAA | 56929 |
| rs372819048 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535284 | CACCATCAAAAAAGT[A/T]AAAAAAAAAAAAAAC | 56929 |
| rs372974163 | in-del | -/GAAAGA | | | cds-indel | FEM1C | GRCh38.p7 | 5:115522973 | AGAGAAAGAGAAAGA[-/GAAAGA]AAGAGTGAGAGAAAG | 56929 |
| rs373137669 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523283 | CTCTTTTTGTAACTA[A/C]AAGTGATTTGCAGTT | 56929 |
| rs373172233 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115540105 | TACTTTTTGAATGGG[A/G]CTAAAAAAGTGGGGA | 56929 |
| rs373194794 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526554 | AACACATTAAGACAT[C/T]GGAAACACCAGGTAT | 56929 |
| rs373297692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115541397 | AAAAGATCACACTTG[C/T]ATCATTTTTATAAAA | 56929 |
| rs373455006 | in-del | -/GA | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522943 | TGTGAGTGAGTGAGT[-/GA]GAGAGAGAGAGAGAG | 56929 |
| rs373460859 | snp | A/C/T | 0.000114169 | 0.00755466 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524274 | CAACTGTTACCAATT[A/C/T]GTGCTTTAACAGTGC | 56929 |
| rs373603980 | snp | G/T | 1.74637e-05 | 0.00295492 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524626 | ACATTCTATCAGTAT[G/T]GCAGTAACTTGTAGA | 56929 |
| rs373605080 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528861 | AGTTTTTTAAAATTG[A/C]GAATTCAACAGAAAA | 56929 |
| rs373922634 | snp | G/T | 1.64738e-05 | 0.00286995 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543133 | CGAAACACGCAGCTC[G/T]AAGAGGAGTTGAATT | 56929 |
| rs374554703 | snp | A/G | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520504 | ACTAGAGCTTTTTGT[A/G]TTAGGCAAGTTAAAC | 56929 |
| rs374783016 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115542772 | AAGTCTTTTATCACA[A/C]TTTTTCAATCTATTA | 56929 |
| rs374955283 | snp | A/G | 3.36027e-05 | 0.00409881 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524320 | TTATCATCTATGAAG[A/G]GAAACAAAAGTCTCT | 56929 |
| rs375149224 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537038 | ACATTATAATTCCCT[G/T]TCCTCTAGTTCACAG | 56929 |
| rs375159711 | snp | A/G/T | 0.000153988 | 0.00877328 | missense | FEM1C | GRCh38.p7 | 5:115525432 | CTAGAGCATTAATAC[A/G/T]TTCTGTCTTGCTGGT | 56929 |
| rs375268276 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545333 | AACCCCATATAAAAC[A/T]ATCAGCTCTCCTGAG | 56929 |
| rs375318510 | in-del | -/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541709 | TACAATGAAATACTG[-/T]ATAGCCACAAAACAG | 56929 |
| rs375344357 | snp | C/T | 1.65699e-05 | 0.00287831 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524479 | GTCACTAGCAGTTTG[C/T]TTGTGCAAGTTTGTG | 56929 |
| rs375355155 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542090 | TCGTATAAATAGATT[C/G]GTGTAAGGGAAGTTA | 56929 |
| rs375592727 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526924 | TAGAATTTTGGGTAT[A/G]AGCTAGGCACAGGGT | 56929 |
| rs375756596 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544417 | CTGTGGCCTCCAGCC[C/T]GCTGCCCGCCTTCGG | 56929 |
| rs376013862 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522469 | CCAATTTACCTTTTC[C/T]TAATGGTGAAATCAA | 56929 |
| rs376068448 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540235 | CCAGAACCAATGAGA[A/G]AATGAGCAGTGAAGC | 56929 |
| rs376136595 | in-del | -/GGT | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546400 | CAAGAGGACTGGCTG[-/GGT]TTTTATCCCCAGCAT | 56929 |
| rs376144772 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545690 | AATGGTAAACCCTAA[A/G]AGCAATGTAAAGTCA | 56929 |
| rs376339394 | in-del | -/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522795 | CTTCATTAAGACATT[-/T]GCAGGGCAAATATGC | 56929 |
| rs376466531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115539482 | TAGGAACCAACTCCC[A/G]TCTCAAAACTCAATT | 56929 |
| rs376703006 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523813 | TGGTAACTGCAAATG[A/G]TAACGAGTCCTTAAG | 56929 |
| rs376730329 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539362 | CACAAACAAAAGAAC[C/G]AAAGGAGGCCAAAGA | 56929 |
| rs376743900 | snp | C/G | 1.65452e-05 | 0.00287616 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543409 | AGGAGGAAACCTCCT[C/G]TTTGGATTTGCTTGC | 56929 |
| rs376838268 | snp | C/T | 3.31735e-05 | 0.00407255 | missense | FEM1C | GRCh38.p7 | 5:115524891 | GTTTGTTTGATAGCT[C/T]GCTCTATTTCAAGGA | 56929 |
| rs376971329 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524052 | CAAAACCAGAATGAA[C/T]AAGCCTTTGGCAGAC | 56929 |
| rs377359271 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546746 | ACACGCACACACACA[C/T]GCACGCACACGCACA | 56929 |
| rs377462396 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533522 | AAGATCATTAAAATC[A/G]TATTTTCTTTTTTGC | 56929 |
| rs377496382 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530832 | GATCATAAAAAGCAC[C/T]AAATAATAAATTAGA | 56929 |
| rs377714654 | snp | C/T | 1.64961e-05 | 0.00287189 | missense | FEM1C | GRCh38.p7 | 5:115525210 | GTGCCTGCATTCTCA[C/T]CTCATCAGGATCAGC | 56929 |
| rs377746478 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541438 | TCTACAGCAAATATG[C/T]TCAGTAACTATATAG | 56929 |
| rs386691397 | multinucleotide-polymorphism | CA/TG | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542222 | AAAATTATACACAAT[CA/TG]AAAACCGGAGCCCTT | 56929 |
| rs397697922 | in-del | -/A | 0 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115535298 | TAAAAAAAAAAAAAA[-/A]CAAACACAGAATGAG | 56929 |
| rs397809788 | in-del | -/A | 0 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115529256 | ATACAACACAGCAAA[-/A]CTGCTGAAAACTAAG | 56929 |
| rs397975633 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528020 | AAAAAAAAAAAAAAA[-/A]GGTAGCAAAAGCCAA | 56929 |
| rs397999045 | in-del | -/T | 0 | 0 | intron-variant | FEM1C | GRCh38.p7 | 5:115542577 | TAGCTTTTTGTTTTG[-/T]TTTTTTTTTTTTTAG | 56929 |
| rs527566606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528835 | AATAACTATGCTTAG[A/C]ATATTCGAGGAGTTT | 56929 |
| rs527593680 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | FEM1C | GRCh38.p7 | 5:115530775 | GCTTCGTCGGTCAAA[C/G]AAGCAAGCCCAATGA | 56929 |
| rs527628551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529722 | ATACCACGAAATTAT[A/G]GAGGGTAATTGGTGT | 56929 |
| rs527650552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528148 | ACAAACAATAAGGAA[A/G]ACTTTCACATCCAGT | 56929 |
| rs527661874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537154 | TTTCATCTGGGTCTC[A/T]CCCTATCTCTTCCAC | 56929 |
| rs527736301 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544272 | ACCCCCCACCCCCCG[A/C]CAAGGGATGATCCGC | 56929 |
| rs527825294 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544944 | GCGGGGCCTGAACTA[C/T]TGGGAGGACGTGCCT | 56929 |
| rs528045607 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FEM1C | GRCh38.p7 | 5:115533235 | TCCTTGGTAAATAGA[A/G]TATTTTCTCATATCT | 56929 |
| rs528144800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540735 | GAAGCTTTGGAAAAT[A/G]TAACGGAAGTAATAC | 56929 |
| rs528198471 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115532462 | TAACCACCACACTTT[C/T]CTGCCCTGGAAGGCC | 56929 |
| rs528237132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115541468 | GTGCCCCATAATTGT[A/G]TGGTTTAACCTTTCT | 56929 |
| rs528579871 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522985 | AGAGAAAGAAAGAGT[A/G]AGAGAAAGAAAGGAA | 56929 |
| rs528644471 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523486 | AAGATGACAGACCTA[A/C]ATTTCAACTGGGTTA | 56929 |
| rs528701829 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523806 | GCACTTATGGTAACT[A/G]CAAATGGTAACGAGT | 56929 |
| rs528733241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538193 | TCTCTCTGTGTAAGT[C/T]AGAAAATTTCCATAA | 56929 |
| rs528748229 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545912 | TCCTGATGAGAAAAC[A/G]GAATTTTTGAAAATG | 56929 |
| rs528992074 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546414 | TGTTTTATCCCCAGC[A/G]TATGTCACAGTTCTA | 56929 |
| rs529016884 | in-del | -/TATG | 0.00199481 | 0.0315187 | intron-variant | FEM1C | GRCh38.p7 | 5:115527017 | TAGAAACATGACACA[-/TATG]TATTTACATTACTGG | 56929 |
| rs529043183 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520411 | TATTAACAATTCAAA[A/C]GGGAAAAACCCATAA | 56929 |
| rs529048945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527469 | TTTAACAATGAGTAA[A/G]CTAACCAAGCACTGA | 56929 |
| rs529064035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115536055 | GGTTGCCTAAGACTA[C/G]TGCAGTTTCAGGGGA | 56929 |
| rs529108074 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543269 | GGTTTCGCCATCAAA[A/G]TTGACGGAGCCCCCA | 56929 |
| rs529545977 | snp | C/T | 1.64961e-05 | 0.00287189 | missense | FEM1C | GRCh38.p7 | 5:115525345 | TGTACCTCATGTTCA[C/T]TGCCTTTTTCCAGTA | 56929 |
| rs529661252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115539396 | CTATAACCATGAAGC[A/G]CTGAGATCACTGTGA | 56929 |
| rs529773448 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546220 | TATGTTTTTACAGTC[G/T]TAATAATTTTTAAGT | 56929 |
| rs529927938 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531517 | TCTCATTATCTCTGG[A/T]ATGAATGATTCACTG | 56929 |
| rs529966133 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534415 | ATAGCTGTATTTTGA[C/G]GAAGAACTAGTTAGA | 56929 |
| rs529984449 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521706 | GACTCAAGAGTGTAA[A/T]TGGTTCATTATTAAA | 56929 |
| rs529989076 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522730 | CTCATTGAACTCACA[A/G]GTAAACTGAGTTTTT | 56929 |
| rs530074187 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115529759 | GTTCTAAGATCTCTT[G/T]CTTGTAAAGACATAA | 56929 |
| rs530143832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528965 | GCTGAATAGAGAATT[A/T]GTAACTGGAAGGTAA | 56929 |
| rs530174656 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115537214 | GCCTCAACAGCATAA[A/G]TCTATGTAATGCCCT | 56929 |
| rs530262007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537927 | AGTTTTTAGTTTACA[A/G]GAGAGATTTTCTCAT | 56929 |
| rs530588530 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535167 | TAAATTCTGCAGTCT[A/C]TTCCTAACAATTTTC | 56929 |
| rs530612328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115533593 | ATATGCCAAGTACTA[C/T]AGATTTAGCTCAAGA | 56929 |
| rs530634568 | snp | C/G | 1.78074e-05 | 0.00298385 | intron-variant | FEM1C | GRCh38.p7 | 5:115525630 | TACCTTAAAGAGAGA[C/G]AGAAAAAAAGAAATA | 56929 |
| rs530976668 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115532126 | CAATTTTATCATTGT[G/T]AGAATGCCTGGTGAA | 56929 |
| rs531101378 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523629 | AGCTATAATAGCTAA[A/C]CTGCAGCTCTAAAAA | 56929 |
| rs531234579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115527731 | AAGCTGGCCAGGCGC[A/G]GTAGCTCACGCCTGT | 56929 |
| rs531268889 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543074 | TGACACTTCCAAATC[A/G]GCTTTGTGTTCTACA | 56929 |
| rs531344055 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FEM1C | GRCh38.p7 | 5:115528024 | AAAAAAAAAAAAGGT[A/G]GCAAAAGCCAATTAA | 56929 |
| rs531516417 | snp | C/G | | | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543671 | TCCAACATCTGACAA[C/G]CAGGGCACCAAACTA | 56929 |
| rs531619228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115535306 | AAAAAAAACAAACAC[A/G]GAATGAGAGAAAATA | 56929 |
| rs531746802 | snp | C/T | 1.65581e-05 | 0.00287728 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543411 | GAGGAAACCTCCTCT[C/T]TGGATTTGCTTGCCA | 56929 |
| rs531753784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544260 | CCCATTTCGATCACC[C/T]CCCACCCCCCGCCAA | 56929 |
| rs532185263 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546759 | CATGCACGCACACGC[A/T]CACACACACAAAAAA | 56929 |
| rs532502326 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522814 | GGGCAAATATGCCAT[C/T]ATAAATTTTATTCTG | 56929 |
| rs532669516 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539605 | CCCTCAGGTTATAAG[C/T]TGTTGGGGATAAAGC | 56929 |
| rs532777320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538017 | TGACTAAAATACATC[C/T]ATATTCTAAATGCCC | 56929 |
| rs532878172 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545675 | ATAAAGGCTACGAGG[A/C]ATGGTAAACCCTAAG | 56929 |
| rs533110269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115527368 | AGTTTATCCTGTTTC[A/G]TCTTCTATGATATCT | 56929 |
| rs533330727 | snp | C/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521206 | AGTGTAAAAGAGTAT[C/G]TCATTATCTCATCCA | 56929 |
| rs533434708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115532293 | CTTATATCCCAGAAG[C/T]AACTAGCAACCTGCT | 56929 |
| rs533458350 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536573 | TAAGAAGGGATAAAG[A/G]GAAAAAAACAACTTA | 56929 |
| rs533681497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115536729 | TAAATTGTGCCAAGA[C/G]TACTTACTATGTGCC | 56929 |
| rs533728603 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530945 | GTAGAAGCAAACAGT[-/A]AAAAAAAAAAAATTA | 56929 |
| rs534025009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527060 | TGCTCTATGTGACCC[C/G]TCACAAGAGGAACAA | 56929 |
| rs534038684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527629 | TAAGAAATAGGCAAT[A/T]TAAGAGAAATCTGAA | 56929 |
| rs534062237 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526191 | ATATCTAAGATTCTT[A/C]ATTTTGACTCTAATA | 56929 |
| rs534144908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534651 | AAAAACAAAAATGTC[C/T]TCCTAAGGACTGCAA | 56929 |
| rs534219290 | in-del | -/AAT | 0.00636936 | 0.0560724 | intron-variant | FEM1C | GRCh38.p7 | 5:115530834 | TCATAAAAAGCACTA[-/AAT]AATAAATTAGATAAA | 56929 |
| rs534290490 | snp | C/T | 1.8812e-05 | 0.00306686 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524276 | ACTGTTACCAATTCG[C/T]GCTTTAACAGTGCTA | 56929 |
| rs534397247 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538337 | GTGCTACTCATTTTT[C/G]TCCAACTACTGTCTT | 56929 |
| rs534408636 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523282 | GCTCTTTTTGTAACT[A/G]AAAGTGATTTGCAGT | 56929 |
| rs534414430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115531619 | AGGTCTCTGTTGTAA[A/C]CACTAAACTCCGCCA | 56929 |
| rs534730890 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540919 | TTCAAACCATTCCCA[A/G]TATTAACATGGTTAG | 56929 |
| rs535024954 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545840 | GCTAAAACCTACGTT[A/G]CATTAAACTAGGATG | 56929 |
| rs535030204 | snp | C/T | 0.000230612 | 0.0107356 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543041 | TGAAATCATCAAGCA[C/T]GTATGCCCATGTCGG | 56929 |
| rs535042358 | in-del | -/A | 0.021333 | 0.101051 | intron-variant | FEM1C | GRCh38.p7 | 5:115541337 | TTACACTTCCTCTGG[-/A]AAAAAAAATTCAGAA | 56929 |
| rs535251036 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531234 | AATATAAAACCAAAC[C/G]TCATAATAGAACTTC | 56929 |
| rs535323008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | FEM1C | GRCh38.p7 | 5:115529537 | AGATCTAAATACTAT[A/G]TGGTGTTCTTTAGGC | 56929 |
| rs535347898 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521282 | GTAAATTCAGCCTAA[C/G]GTTTCTGTTGGGCAA | 56929 |
| rs535378220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115525687 | TGTAATATATATATG[C/T]ACTTTAGAACCTAAA | 56929 |
| rs535456704 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115538821 | CTTATGCCATTTCCT[A/C]AACCTTCAAAACTGC | 56929 |
| rs535548936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541295 | TTTGGAAGTATTATC[C/G]CTGAGTACTGGGATT | 56929 |
| rs535585534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541869 | ATGCTTGTATTTGCA[C/T]AGACCAACTCTAAAA | 56929 |
| rs535748019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115526632 | ATTATCATGCCGACC[G/T]CTGGTATTTACATAC | 56929 |
| rs535940595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537637 | TTACAGGAGTAACTT[C/T]ATAATTTGGGATTAA | 56929 |
| rs536011102 | snp | C/T | | | intron-variant, synonymous-codon | FEM1C | GRCh38.p7 | 5:115529570 | AAGGAAGATGAGCCA[C/T]GTGGAAGCCTGGAGA | 56929 |
| rs536052695 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545497 | CTCACACACGTGAAG[A/T]CTCTCGGACTAGTCT | 56929 |
| rs536221183 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521123 | AAAATGATGATGACC[A/G]ATTAGTTTGTTTCCT | 56929 |
| rs536273573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530021 | AAATGTAAGTAAACT[A/G]AATGTTTAATTTAAA | 56929 |
| rs536474939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527695 | TCAGAGTAGCACAAA[A/G]TCAAGAATAAAATGT | 56929 |
| rs536508304 | in-del | -/CTTAT | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522884 | TTTTAGTACTTTTCA[-/CTTAT]CTTAAGTTAAAAGAG | 56929 |
| rs536576612 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FEM1C | GRCh38.p7 | 5:115535706 | TAACGGTTCCTGTTA[A/G]AAGAGTTACCATACA | 56929 |
| rs536857987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115536493 | TGTGGTTCAATTGCA[C/T]AATAATGCTGATTCC | 56929 |
| rs536977307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544374 | CCAATCTCCTCCATC[A/G]ACCACAACCCCCTCC | 56929 |
| rs536983180 | in-del | -/AC | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536348 | CATTTATTTGGAAAG[-/AC]ACAAAAACAGTCCTC | 56929 |
| rs537340603 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FEM1C | GRCh38.p7 | 5:115540238 | GAACCAATGAGAGAA[C/T]GAGCAGTGAAGCTTC | 56929 |
| rs537357053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115531825 | TACTGAAATGGGGTG[A/G]GCTGGATTTGAACCC | 56929 |
| rs537427726 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546583 | GGGATTGTTAAGGGA[C/T]AGACGGACACTTAGT | 56929 |
| rs537570699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115543808 | CACTACTCCATCCCA[C/T]ACACCCCCCCCACCC | 56929 |
| rs537698210 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538380 | CAAGTCTTCATGCAT[A/G]TATTTATTTCCCTAC | 56929 |
| rs537877766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115526692 | CATTTTAGGCATGTC[C/T]GTAGAAAAGAGGTAG | 56929 |
| rs537899575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115533759 | ACACAAAGTTCAAAA[A/G]TAAATATTACCAGGA | 56929 |
| rs537985210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534563 | ATTTAGATAAAATTA[C/T]CAAGATTCACCAGGA | 56929 |
| rs538061980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541920 | ATAGTGGTTGTCAGC[A/G]CATTAGAGATCTAGA | 56929 |
| rs538174588 | snp | A/C | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522350 | TGGTCTAAATCATAA[A/C]GTATTCTTAATATAT | 56929 |
| rs538220624 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523218 | ATACCTTAATTATCC[C/T]AGATGCCTAGATCTG | 56929 |
| rs538468653 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546353 | GAATAGAGTATAAAG[A/G]ATAAGATTGACCATC | 56929 |
| rs538841133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538434 | CTTGCCATCAAGGAG[C/T]TTATAATCTTTCCTC | 56929 |
| rs538887813 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520761 | GTACATAAATCATAC[C/T]TACATAGAAGTATTA | 56929 |
| rs538975008 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532367 | AAAGTAATTCAATCT[C/T]AGCTTTTGCAGACAA | 56929 |
| rs539016751 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546524 | TTCAATAAGATGTAA[A/G]CATTCACATCAGCCA | 56929 |
| rs539354581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528418 | TAGAGGGGAAAAGTG[A/G]AGCCTACAGCCTACT | 56929 |
| rs539464115 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541204 | TTAAAGATAACATTT[A/C]TTAAGCTAAAAAACA | 56929 |
| rs539488501 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532500 | TAAGTTTTTTAATTA[C/T]AGCCTAGAGCATTAT | 56929 |
| rs539618373 | snp | A/G | 1.99846e-05 | 0.003161 | intron-variant | FEM1C | GRCh38.p7 | 5:115525659 | TAACATACATTGAGG[A/G]ACCAAAATATAATGT | 56929 |
| rs539730529 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523665 | ATGCTACAGAGTACT[G/T]TCAAAAAATTAAGTT | 56929 |
| rs539742299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115532748 | CATAATCCTTCTTAA[C/T]GGTTTTATGGTGAAA | 56929 |
| rs539753880 | snp | A/G | 1.76157e-05 | 0.00296775 | stop-gained | FEM1C | GRCh38.p7 | 5:115524637 | GTATTGCAGTAACTT[A/G]TAGAGATGGAAATTT | 56929 |
| rs539755776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115533597 | GCCAAGTACTATAGA[A/T]TTAGCTCAAGAATTT | 56929 |
| rs539950128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540354 | TGAAAAGGTAAAAAT[C/T]CTGCACATGAAGTGA | 56929 |
| rs540022843 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543082 | CCAAATCAGCTTTGT[G/T]TTCTACAAGGTACTT | 56929 |
| rs540060468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115535115 | ACAAAGTTTCATCCA[C/T]GGAAAAGTTCCTGCA | 56929 |
| rs540316158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115536011 | TAAATGTCCAGAACA[A/G]GCAAACTTAAGACAG | 56929 |
| rs540326863 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523327 | TTTCAATGTGACTCA[C/T]TAAGCTGTGTGATGA | 56929 |
| rs540349003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527827 | CCAACATGGTAAAAC[C/T]TTGTCTCTACTAAAA | 56929 |
| rs540481081 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546845 | GGGGAGATCAAGGCT[A/G]TAGTGAGCCATGATC | 56929 |
| rs540544424 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525232 | AGGATCAGCAATAAG[A/G]CCTTCTAGCTCTTCT | 56929 |
| rs540941643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115533832 | AATTTACCTTTGGCT[A/G]AAGAAAAAAAAGGAA | 56929 |
| rs540990989 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531293 | AAACTTTCACAATTT[A/C]TCTAAGGAAAAGCAG | 56929 |
| rs541060251 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534048 | AATTCTGTTAAAGCA[C/T]TTCTCTAGAAAGCTA | 56929 |
| rs541275185 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115529733 | TTATGGAGGGTAATT[A/G]GTGTTAACGTGTTCT | 56929 |
| rs541423271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537901 | TTATCTTAGTCTATC[C/T]GAATACCAACAGTTT | 56929 |
| rs541520237 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544956 | CTACTGGGAGGACGT[A/G]CCTGCGTGCAACGCG | 56929 |
| rs541739751 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520892 | CAAGTATTGAGTTAA[C/T]AAGAATACACTTAAA | 56929 |
| rs541740676 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538477 | CATGTCCACTCAACA[A/G]GCTCATTTAGGGCCA | 56929 |
| rs541817391 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542092 | GTATAAATAGATTCG[A/T]GTAAGGGAAGTTAAG | 56929 |
| rs541831154 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527740 | AGGCGCGGTAGCTCA[C/G]GCCTGTAATCCCAGC | 56929 |
| rs541854208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542822 | TCAACAAAGTCATAC[C/T]GGAAGACTTACCTAA | 56929 |
| rs541913713 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FEM1C | GRCh38.p7 | 5:115531996 | CTTCCACCTCTATGC[C/G]TCTGTTCTTGATTTT | 56929 |
| rs541977098 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524099 | ATGTTACATTTCTCA[A/G]TAATTCACAAACAAT | 56929 |
| rs542100601 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546699 | GAGGTCGAGACCAGC[C/G]TGGACAACATGGTGA | 56929 |
| rs542239144 | snp | A/G | 3.61912e-05 | 0.00425374 | missense | FEM1C | GRCh38.p7 | 5:115524756 | TTAAGAAACCTGTAT[A/G]TAGTCTGCTTTTTGA | 56929 |
| rs542284539 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521429 | CTTCAAATTCATAAT[C/G]GGCACCAAATTATCT | 56929 |
| rs542313858 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542723 | TTTAAGTTACTCCAA[A/G]TAAGAGAGAAAATAC | 56929 |
| rs542326800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115532927 | AGGAGAGGGGTTTAA[A/T]GCAAAGGAGCATGAA | 56929 |
| rs542372481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529611 | AACATCAACAAAAAG[A/G]GTAAATTTGTGAGTA | 56929 |
| rs542379952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115539900 | GTAATGAAAAGAGGT[A/T]AAATAACATGTTCAA | 56929 |
| rs542385584 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544778 | CGACGGATGGTGTAA[C/T]GGGCTGCGAGCCGGG | 56929 |
| rs542385817 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FEM1C | GRCh38.p7 | 5:115536058 | TGCCTAAGACTAGTG[C/T]AGTTTCAGGGGAATG | 56929 |
| rs542424169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115536899 | GAGGGAGATGAAGAA[C/T]TGCATTTGAAATGAG | 56929 |
| rs542451416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115531193 | AAATGCCAGTCATAT[C/T]AAACCTCAATGAATA | 56929 |
| rs542498075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544091 | GGGCGCCAGGCTGGA[A/G]GGCCTGAGGCCGGGT | 56929 |
| rs542660448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528620 | AGCCAGAAGCAAATA[C/T]AAATACTATTTAGAG | 56929 |
| rs542721752 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115520945 | TAAACCTTACAATGA[A/G]TGTTGTGGCATATGA | 56929 |
| rs542763781 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527819 | CATCTTGGCCAACAT[A/G]GTAAAACCTTGTCTC | 56929 |
| rs543204417 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530444 | ATCTGCAAACATTAG[G/T]ACATCTAAACATATC | 56929 |
| rs543301953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534911 | TTATTTTCTTGTTTG[C/T]TATATAGATACTTGC | 56929 |
| rs543322075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527181 | TAATAAATCTTACCT[A/G]TGAGTACAGTTATAT | 56929 |
| rs543813220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538724 | AATGTCCTTTAAAAT[G/T]CAGCCCTGAGTGCCT | 56929 |
| rs543834689 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522055 | ACTTTACACAGGAGT[G/T]GCACAATTCAAATTC | 56929 |
| rs544079008 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545644 | GACTCTCTTTCTAAA[G/T]TAGCCTCTAAAAAGC | 56929 |
| rs544201964 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528542 | GCAAAAACTTAAATC[A/G]AATTTAAGATCATCT | 56929 |
| rs544240292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115535861 | AAAAGTGATATATCT[A/G]TTTCAATGGAATATT | 56929 |
| rs544261801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527331 | AAACAAGTTATTATA[A/C]GAAATATTGAATCTT | 56929 |
| rs544331017 | snp | C/T | 6.63548e-05 | 0.0057596 | missense | FEM1C | GRCh38.p7 | 5:115524886 | ACTGAGTTTGTTTGA[C/T]AGCTCGCTCTATTTC | 56929 |
| rs544349970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115535037 | TAAAATTGTATCATT[C/G]CTCTTTACTCTAAGT | 56929 |
| rs544440852 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115533030 | AAGTATGAATTTTAT[A/T]GCATGTAAATAAGTC | 56929 |
| rs544491783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540598 | AGGGAACATTGTTTT[A/G]AAAGAGCTCAAAGGT | 56929 |
| rs544520556 | in-del | -/A | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523905 | CAATAAAGTAGAAAC[-/A]GGGGGGAAACTTGAG | 56929 |
| rs544528690 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115532195 | TCTACTATTATAATA[C/T]CTTACACTAGTATAA | 56929 |
| rs544714934 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522409 | TCCCACAGTGAGAGA[C/T]AGTAAAACCTCTTCA | 56929 |
| rs544839431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529667 | AATAATATCTTGTAG[G/T]GCTTGAAATACATAC | 56929 |
| rs544964812 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545560 | CCAAGCTCGTAATTA[C/G]ACCTCAGAACACACA | 56929 |
| rs545387406 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544883 | GCCAGCAACAGCCTA[A/G]GCGCGGGGCGGGGCG | 56929 |
| rs545487624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541442 | CAGCAAATATGCTCA[A/G]TAACTATATAGTGCC | 56929 |
| rs545531509 | snp | A/C | 0.0138799 | 0.0821421 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523190 | ATATTATGGCAGTAA[A/C]TTGCATACTAAAATA | 56929 |
| rs545759692 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541950 | AAATCAGGAATAAGA[C/T]TTTTTATTCAAATGT | 56929 |
| rs545972364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115539775 | TATTGCTCTTTGTAT[A/T]TCCTAAGTCTAACAG | 56929 |
| rs546022141 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539427 | TAGCTCTGAGAAGGA[C/G]TCACCTAATCACTAC | 56929 |
| rs546085138 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546651 | AATCCCAGAACTTTC[A/G]GAGGCTGAGACAGGC | 56929 |
| rs546117427 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523988 | ACCAGTAAAGTATAA[A/G]GACACCATGGAGAAA | 56929 |
| rs546218697 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536094 | GGATAGGAGGGAGTG[A/C]CTCTTAATGGATATG | 56929 |
| rs546253963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115531871 | CAAACCTGCTCTAAC[C/T]CGGAGACATGGTCTG | 56929 |
| rs546291691 | snp | C/T | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520521 | TAGGCAAGTTAAACA[C/T]AAAAAAAACAAGGAC | 56929 |
| rs546341654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115531064 | TAACTTTGCAAGGTA[A/G]AGATGATAAACTCAT | 56929 |
| rs546344763 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545995 | CCACTAGGAGAAATA[C/G]AATATTACAGTAGGC | 56929 |
| rs546546415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FEM1C | GRCh38.p7 | 5:115533662 | CATAATACAGCGATC[A/G]TACTTCCCAAAGATT | 56929 |
| rs546675023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527431 | TTCAATGGTCTACAA[C/T]GAAATAGTGTTTGAT | 56929 |
| rs546743075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534390 | TTTTCAAATTAGGTA[A/C]CCCAAAAACATAGCT | 56929 |
| rs546835351 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546041 | ATATGTAATCCATAA[C/T]GTTATGTTAGAAGTC | 56929 |
| rs546856602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542261 | ACAAAGGTGTTTACA[C/T]TGTTGCTAGCCAACA | 56929 |
| rs546949667 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545713 | TAAAGTCAATGAGGT[C/T]AGGTTCTTGAGCTCT | 56929 |
| rs547245272 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521070 | AGTTGTTTAGTGACA[C/T]ATAAGGGCAAAAAAA | 56929 |
| rs547324407 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115525888 | AATCCATGGTCTCTT[C/T]GTATTTTTCATTAAT | 56929 |
| rs547517404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528884 | ACAGAAAACTGGAAA[C/T]TAATCAAGTAGACAT | 56929 |
| rs547569206 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | FEM1C | GRCh38.p7 | 5:115533363 | GTTTGTTAAATTTAC[C/T]GTAAATATTTTGCTA | 56929 |
| rs547654160 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529141 | TATTTAAGAAAAGAT[-/A]AAAGTCCAAGAATTT | 56929 |
| rs547749140 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115528186 | GAGATACCTGTAACA[G/T]GATCACCCTCCCACT | 56929 |
| rs547819386 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536038 | ACAGAAAAGAGATTA[C/T]TGGTTGCCTAAGACT | 56929 |
| rs547969572 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543572 | TCGACACAGGCAAGA[A/G]TCACAGGAACCAAAG | 56929 |
| rs548026247 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531630 | GTAACCACTAAACTC[C/T]GCCAAGTACCATGAA | 56929 |
| rs548056793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544347 | CCTGTTCCAGACAAC[A/G]GCAGCCCCCTCCCAA | 56929 |
| rs548146243 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FEM1C | GRCh38.p7 | 5:115533327 | CTTTCTATGTATAAG[C/G]ACTTTATAAAATGAT | 56929 |
| rs548208267 | snp | C/T | 4.95193e-05 | 0.00497566 | missense | FEM1C | GRCh38.p7 | 5:115525431 | TCTAGAGCATTAATA[C/T]GTTCTGTCTTGCTGG | 56929 |
| rs548757043 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520506 | TAGAGCTTTTTGTAT[C/T]AGGCAAGTTAAACAT | 56929 |
| rs548828352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529961 | CAAATAAAAATCAGA[A/G]AAGTACCCAGGAGAT | 56929 |
| rs548841991 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523108 | AGTAATCAAAGTAAT[C/T]CATGCAAGTTATCTT | 56929 |
| rs548851808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115535233 | ATTTCCTTAAAAATC[A/C]GTTTGTAAAATAAAA | 56929 |
| rs549043923 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521667 | CCAGTCAATAACACC[A/G]TGCTACAGTGTACAG | 56929 |
| rs549157590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534461 | TGGGTCCAAACCAAA[C/T]GTTTTGAGTTTGATA | 56929 |
| rs549588355 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546263 | TTCCCTTAGGTAGTC[A/C]GTATCAGACTACACT | 56929 |
| rs549713664 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546750 | GCACACACACATGCA[C/T]GCACACGCACACACA | 56929 |
| rs549845332 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528063 | TATTTCTGTATTTAT[C/T]GAAAAAATACAAAAT | 56929 |
| rs549882818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529761 | TCTAAGATCTCTTTC[C/T]TGTAAAGACATAAAA | 56929 |
| rs549946214 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521771 | TTAAGTATTTTATTA[A/T]AATCCATCTCATAAT | 56929 |
| rs550042560 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537605 | TACAAGAGGGAAAAG[A/C]ATGAACACAGAGCAA | 56929 |
| rs550272733 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521126 | ATGATGATGACCAAT[C/T]AGTTTGTTTCCTTAG | 56929 |
| rs550373347 | snp | C/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546461 | AGATAACAGTGTACA[C/G]TGTCCCAACCAAGGC | 56929 |
| rs550397562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537242 | CCTGGGTTTCCTGAA[C/T]TTTATTTCAAACAAA | 56929 |
| rs550470310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544383 | TCCATCGACCACAAC[C/G]CCCTCCCGATGGGCC | 56929 |
| rs550716839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541706 | TCATACAATGAAATA[C/G]TGTATAGCCACAAAA | 56929 |
| rs550841714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115533594 | TATGCCAAGTACTAT[A/G]GATTTAGCTCAAGAA | 56929 |
| rs550872102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540982 | TTCTTCAAAAGAATG[A/G]TAATTGTTTGGAGAA | 56929 |
| rs551016197 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523631 | CTATAATAGCTAACC[G/T]GCAGCTCTAAAAATT | 56929 |
| rs551312875 | snp | C/G | | | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543672 | CCAACATCTGACAAC[C/G]AGGGCACCAAACTAG | 56929 |
| rs551328180 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115535347 | ATATATCTGATAAAA[A/G]ACATACATAAGAATA | 56929 |
| rs551453577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544264 | TTTCGATCACCCCCC[A/G]CCCCCCGCCAAGGGA | 56929 |
| rs551737315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115531536 | AATGATTCACTGTGC[A/G]TCTAACTCAGGGACT | 56929 |
| rs551800682 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115532324 | AAAGCTAAGGTAGAT[G/T]CTAAATTTTTAATAT | 56929 |
| rs552119224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540721 | CACAAGTACATAAAG[A/C]AGCTTTGGAAAATAT | 56929 |
| rs552462237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115538098 | ATAGAAAACAAAAGG[A/G]AAGTAGAAACTTTTT | 56929 |
| rs552559996 | snp | C/T | 1.88959e-05 | 0.00307369 | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543527 | CTGTGCTTTATTTAT[C/T]TTTCAAAGCAGAGCT | 56929 |
| rs552576288 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545685 | CGAGGAATGGTAAAC[C/T]CTAAGAGCAATGTAA | 56929 |
| rs552583126 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538440 | ATCAAGGAGCTTATA[A/C]TCTTTCCTCTCTTAA | 56929 |
| rs552620164 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541213 | ACATTTATTAAGCTA[A/C]AAAACAGGTTATAGA | 56929 |
| rs552725805 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522938 | AAATCTGTGAGTGAG[C/T]GAGTGAGAGAGAGAG | 56929 |
| rs552850201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529874 | CTACATTTTCTCTAA[C/T]ATATAGAAAAAAATG | 56929 |
| rs553213578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540360 | GGTAAAAATTCTGCA[A/C]ATGAAGTGACAATAT | 56929 |
| rs553337114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115532758 | CTTAATGGTTTTATG[A/G]TGAAAGTTCAAGCAA | 56929 |
| rs553472771 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545488 | AGTATTACCCTCACA[C/T]ACGTGAAGTCTCTCG | 56929 |
| rs553587316 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544663 | TCCATGCTCCGCGCC[C/G]CAAAGGAATGAATCC | 56929 |
| rs553718926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115528554 | ATCGAATTTAAGATC[A/G]TCTCATTATTGATTT | 56929 |
| rs553947571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527119 | TCTACACTTCACCTG[C/T]GGCTTTACCCCTCAT | 56929 |
| rs554179710 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532383 | AGCTTTTGCAGACAA[A/C]ATAAGTTCAAAAAGT | 56929 |
| rs554455591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530801 | AATGAAAATCAGAAA[A/T]TTTTTTTAACTGGGT | 56929 |
| rs554561544 | in-del | -/ATG | 0.00119737 | 0.0244387 | cds-indel | FEM1C | GRCh38.p7 | 5:115524200 | GCCAATGAGAGCACA[-/ATG]ATATCAATCAAGCTA | 56929 |
| rs554750697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115531631 | TAACCACTAAACTCC[A/G]CCAAGTACCATGAAA | 56929 |
| rs555040318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538650 | CCACTCCAGTTAGTC[C/T]CCTGCTGAAAAACTT | 56929 |
| rs555193840 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115530465 | TAAACATATCTTTCT[C/G]AGTTTAGAAGACCAA | 56929 |
| rs555232475 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533043 | ATTGCATGTAAATAA[C/G]TCAATAAACAAATGA | 56929 |
| rs555355191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542886 | CACCAGTGCTTATAA[A/T]GATGTATCAAACTTC | 56929 |
| rs555409256 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526604 | AAACATTTTACTAAT[A/C]GTCAAAATAGGAATT | 56929 |
| rs555441276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534915 | TTTCTTGTTTGCTAT[A/G]TAGATACTTGCCACA | 56929 |
| rs555553879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115532971 | CTTACCTTTAATAAA[G/T]GCGTAGTATATGTTT | 56929 |
| rs555725679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530120 | GTCAGACTGAAGATA[C/G]AAAGAAAACTCAAGA | 56929 |
| rs555739129 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539881 | GCCAATAGCCTGTTA[A/G]AAAGTAATGAAAAGA | 56929 |
| rs555817531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115538416 | GGCCTATAAAACATA[A/G]TGCTTGCCATCAAGG | 56929 |
| rs555981123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537713 | CAAAATAAATATAGA[C/T]ATATTAGAATAAGTC | 56929 |
| rs556037405 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545503 | CACGTGAAGTCTCTC[A/G]GACTAGTCTTCCGTC | 56929 |
| rs556056295 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544793 | TGGGCTGCGAGCCGG[A/G]GGCCGGACAAGCCTG | 56929 |
| rs556109913 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521447 | CACCAAATTATCTTT[G/T]ATTTGGGTTTATGCC | 56929 |
| rs556311116 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529876 | ACATTTTCTCTAACA[C/T]ATAGAAAAAAATGAA | 56929 |
| rs556344086 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520733 | CTACTAGAAAAAAAA[A/T]TTAGAATAAACTGTA | 56929 |
| rs556362114 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545769 | TAAAAGGTTATATAT[A/G]TGAATGAAAAGAATT | 56929 |
| rs556461051 | in-del | -/CTC | 0.00358779 | 0.0422022 | cds-indel | FEM1C | GRCh38.p7 | 5:115522578 | CTTGTTTATTTACTA[-/CTC]CTCATTACAAGGTTT | 56929 |
| rs556511005 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526916 | TGGGAGTCTAGAATT[C/T]TGGGTATGAGCTAGG | 56929 |
| rs556529201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528333 | GAGGCAGCTTTCCCA[C/G]AGTGGCCTCCACCAA | 56929 |
| rs556568974 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544755 | TGCAGCGGCTGCAGC[A/G]ACTGCTGCGACGGAT | 56929 |
| rs556824466 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | FEM1C | GRCh38.p7 | 5:115535334 | TATTTGCAAATGATA[-/T]TATCTGATAAAAGAC | 56929 |
| rs556871638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115535733 | TACAACCCAATAATG[C/T]CACTCCTAGGTATGT | 56929 |
| rs557177550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115532700 | ATGTGTTATTACATC[A/G]TCTGCATAGTTTCTG | 56929 |
| rs557425114 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544431 | CCGCTGCCCGCCTTC[G/T]GCTCCCCCGGCGCCC | 56929 |
| rs557432415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540281 | GAGGAGGATGAACAT[A/G]TACTTTAATCTGCCC | 56929 |
| rs557740133 | snp | A/C/T | 0.00319106 | 0.0398404 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544998 | GGCGCTGCGAGGGGG[A/C/T]GGATCTGTGCCCATC | 56929 |
| rs557742699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115535878 | TTCAATGGAATATTA[C/T]TCTGCAATAAAAAGA | 56929 |
| rs557772719 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532312 | TAGCAACCTGCTAAA[C/G]CTAAGGTAGATTCTA | 56929 |
| rs557810417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534600 | CAGTTTCTAAACCAC[A/C]CTCACGGAGTAGACA | 56929 |
| rs557830520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115536610 | CAAAGGAGCACTAGA[A/G]GAAGGATTCTCTGCT | 56929 |
| rs557856356 | in-del | -/CTTGTATCATTTTTATAAAAGATCACA | 0.00279162 | 0.0372561 | intron-variant | FEM1C | GRCh38.p7 | 5:115541366 | AAAAATCACAATGAT[-/CTTGTATCATTTTTATAAAAGATCACA]CTTGTATCATTTTTA | 56929 |
| rs557919191 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545577 | CCTCAGAACACACAC[A/G]GAGGAAACTGAAATT | 56929 |
| rs557945536 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520592 | TATAAAATTTGCATT[C/G]ATAATAATATATTTA | 56929 |
| rs558197689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530779 | CGTCGGTCAAAGAAG[C/G]AAGCCCAATGAAAAT | 56929 |
| rs558199348 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522465 | ATATCCAATTTACCT[C/T]TTCTTAATGGTGAAA | 56929 |
| rs558244314 | in-del | -/AAAT | 0.0023933 | 0.0345097 | intron-variant | FEM1C | GRCh38.p7 | 5:115541773 | CATCCAAGGTTAGAA[-/AAAT]AAATAAAGATAAAAA | 56929 |
| rs558379467 | in-del | -/TTTA | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537743 | CCCTCCCTTCCCCCT[-/TTTA]TTTTTCTCTGTAAGT | 56929 |
| rs558594373 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533575 | GTTTTGGTGCATAAC[A/G]ATATATGCCAAGTAC | 56929 |
| rs558761350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115539503 | AAACTCAATTGCTAT[C/G]ACTGTTAAACTGAAG | 56929 |
| rs558919755 | in-del | -/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534391 | TTTCAAATTAGGTAA[-/C]CCAAAAACATAGCTG | 56929 |
| rs559194072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540734 | AGAAGCTTTGGAAAA[C/T]ATAACGGAAGTAATA | 56929 |
| rs559263774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528422 | GGGGAAAAGTGGAGC[C/T]TACAGCCTACTAAGA | 56929 |
| rs559299107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115541457 | GTAACTATATAGTGC[C/T]CCATAATTGTGTGGT | 56929 |
| rs559518965 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546689 | TTGAACCCAAGAGGT[C/T]GAGACCAGCCTGGAC | 56929 |
| rs559774948 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523451 | TTAAAAAGATTCTTC[C/G]TTTTACTGCATGATA | 56929 |
| rs559859288 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523801 | ATAAAGCACTTATGG[C/T]AACTGCAAATGGTAA | 56929 |
| rs559915158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543992 | TTTGCTTTGCACACG[C/T]CCAGGGAGAGTACAA | 56929 |
| rs559936129 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529847 | CTAAAATAATAGAGG[G/T]TATGCACATAACTAC | 56929 |
| rs560016536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527877 | ATGGTGGCACGCGCC[C/T]GTAGTCCCAGCTACT | 56929 |
| rs560192921 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520902 | GTTAATAAGAATACA[C/G]TTAAATTTGGTGCAA | 56929 |
| rs560303627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115526026 | ATAAACAAGGAATTG[A/G]TCTTTTTTTTTTTCT | 56929 |
| rs560308360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115527468 | TTTTAACAATGAGTA[A/G]GCTAACCAAGCACTG | 56929 |
| rs560441200 | snp | A/C | 6.59794e-05 | 0.00574329 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525256 | CTCTTCTGCACTGTT[A/C]ACTTCCTTGGCATAA | 56929 |
| rs560537161 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546199 | TTCTATACTCTAAAC[A/G]TTTCTTATGTTTTTA | 56929 |
| rs560733194 | in-del | -/ATA | | | cds-indel | FEM1C | GRCh38.p7 | 5:115524174 | GTAAATTTGATGCTT[-/ATA]ATGCTTTAGCCAATG | 56929 |
| rs560738420 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522635 | CCTAATGTGACTGTT[G/T]GCATTGATGACTCCT | 56929 |
| rs560881253 | snp | C/T | 1.67756e-05 | 0.00289612 | missense | FEM1C | GRCh38.p7 | 5:115524582 | AGGGGACTGTTGTCA[C/T]CCGAGTCTCTGACGT | 56929 |
| rs560920227 | in-del | -/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527943 | AGGTGGAGGTTGCAG[-/T]TAAGCAGAGATCATG | 56929 |
| rs561261737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530312 | AAAGGAAATATTTTA[C/T]AATGTTAAAAAATTC | 56929 |
| rs561446932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537176 | CTCTTCCACTTCTAT[C/T]TTCCATCACATACAT | 56929 |
| rs561620230 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FEM1C | GRCh38.p7 | 5:115534208 | AAACTATGGTAAGTG[C/T]TCGTGCATTAAAGGG | 56929 |
| rs561780653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542135 | CAAAATTATGCTATC[A/C]AGGCAGTTGCTTTTA | 56929 |
| rs561801360 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115527904 | TACTTGGGAGGCTGA[C/G]GCAGGAGAATCACTT | 56929 |
| rs561892206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541557 | ACACAGGTATTTATA[C/T]TACAGTTATTCTCAC | 56929 |
| rs561897585 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FEM1C | GRCh38.p7 | 5:115540568 | TATAAGGCTAAAAGA[C/T]GATAGTGGTGATAAA | 56929 |
| rs562228455 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533969 | ATTTCATGATTTCTC[A/G]AAAGACATGTTTGTT | 56929 |
| rs562414211 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115520950 | CTTACAATGAATGTT[A/G]TGGCATATGATTTTC | 56929 |
| rs562458408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115536120 | ATATGAGATTTTTTC[C/T]GGGGGTGATGAAAAG | 56929 |
| rs562487465 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523911 | AGTAGAAACAGGGGG[G/T]AAACTTGAGAAGAGA | 56929 |
| rs562550947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528655 | ATATTATCATATTAG[A/G]GTTCAAATTATTTAT | 56929 |
| rs562570690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544254 | GCCCGCCCCATTTCG[A/G]TCACCCCCCACCCCC | 56929 |
| rs562698430 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FEM1C | GRCh38.p7 | 5:115528022 | AAAAAAAAAAAAAAG[C/G]TAGCAAAAGCCAATT | 56929 |
| rs562712484 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520537 | AAAAAAAACAAGGAC[G/T]ACTTAGATTTTACAA | 56929 |
| rs562777532 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521049 | CTGACAAAAGGGAGA[A/G]AAACTAGTTGTTTAG | 56929 |
| rs563156069 | in-del | -/TACTC | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535043 | TGTATCATTCCTCTT[-/TACTC]TAAGTTTAACCATAT | 56929 |
| rs563327088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115540610 | TTTGAAAGAGCTCAA[A/G]GGTAATCAAGTTAAA | 56929 |
| rs563511183 | snp | A/C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542840 | AAGACTTACCTAATC[A/C/G]AAACAGGTCTGTCAA | 56929 |
| rs563571405 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523363 | GAAGTTAAATTTAAG[C/T]AAATTCTCTACACCT | 56929 |
| rs563609143 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522116 | TAAGAGCATGTAAGC[C/T]CTCCCACCCAGCCCC | 56929 |
| rs563668176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115530446 | CTGCAAACATTAGTA[C/T]ATCTAAACATATCTT | 56929 |
| rs563791182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538805 | CTTCAAAGTGCCTTT[C/T]CTTATGCCATTTCCT | 56929 |
| rs564064425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527361 | TTCCACAAGTTTATC[C/T]TGTTTCGTCTTCTAT | 56929 |
| rs564076519 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115527750 | GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 56929 |
| rs564157293 | snp | A/C | 1.77084e-05 | 0.00297554 | intron-variant | FEM1C | GRCh38.p7 | 5:115542901 | TGATGTATCAAACTT[A/C]CTGAAAATAAGTGGT | 56929 |
| rs564348258 | snp | A/G | 1.65037e-05 | 0.00287256 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525069 | TCTGCTGCATATCCA[A/G]AGCATACTTCCATAG | 56929 |
| rs564519516 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524171 | GTTGTAAATTTGATG[C/G]TTATAATGCTTTAGC | 56929 |
| rs564644205 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115541420 | TTATAAAAGATCACA[A/C]AATCTACAGCAAATA | 56929 |
| rs564743433 | snp | A/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521489 | TGAATAAGAAAAATG[A/T]CTATTTTTAAGTCTA | 56929 |
| rs564865837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528803 | ATAATGCAGTTTATC[A/T]ACACAGATTTTCAAA | 56929 |
| rs565168855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115537138 | TGCATCCAACTGACT[C/T]TTTCATCTGGGTCTC | 56929 |
| rs565206166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537784 | CTGAGGTAACCAACA[G/T]CTGAGAAGAGTTTTC | 56929 |
| rs565491033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115532444 | TCTAACAGGTTAAGT[A/G]TATAACCACCACACT | 56929 |
| rs565845827 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115525988 | TGACAAGTCACTTAA[C/T]TTCCAGGTCAGTTTC | 56929 |
| rs566060716 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536102 | GGGAGTGACTCTTAA[C/T]GGATATGAGATTTTT | 56929 |
| rs566192634 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540149 | GCTGCTAAATCACAT[A/C]CTTCTCCAGTGTCCC | 56929 |
| rs566204005 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522975 | AGAAAGAGAAAGAGA[A/C]AGAAAGAGTGAGAGA | 56929 |
| rs566230208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115529907 | ATAATAATCCAAAAG[C/T]GGCAAAAAAGAAGAC | 56929 |
| rs566266204 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531092 | CATTCTACATACAAA[C/T]AGAAAAGAGAATTTA | 56929 |
| rs566291308 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522012 | ATCTATTTTTACTGG[A/T]GCAAAAATGCTATTT | 56929 |
| rs566373410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538149 | TAATTGTTGAAGTAA[A/G]ATGATGAATACATAG | 56929 |
| rs566403078 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521370 | GTAGACTGGGGTCTC[C/T]ATACACATTAAGGTA | 56929 |
| rs566665942 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534420 | TGTATTTTGAGGAAG[A/T]ACTAGTTAGAGGCCT | 56929 |
| rs566672325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115526628 | AGGAATTATCATGCC[A/G]ACCTCTGGTATTTAC | 56929 |
| rs566847203 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FEM1C | GRCh38.p7 | 5:115541855 | GTACATAGACAAGTA[C/T]GCTTGTATTTGCATA | 56929 |
| rs566882459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115533677 | GTACTTCCCAAAGAT[C/T]TTCCATCTCCACATC | 56929 |
| rs567335036 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521115 | AAAAAAAGAAAATGA[G/T]GATGACCAATTAGTT | 56929 |
| rs567459913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115529713 | TTGACAGCAATACCA[C/T]GAAATTATGGAGGGT | 56929 |
| rs567649108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528948 | AAGTGGATTTACACA[C/T]AGCTGAATAGAGAAT | 56929 |
| rs567959573 | snp | A/T | 3.30104e-05 | 0.00406252 | missense | FEM1C | GRCh38.p7 | 5:115525438 | CATTAATACGTTCTG[A/T]CTTGCTGGTCTGTGC | 56929 |
| rs568120176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115531646 | GCCAAGTACCATGAA[A/G]TATGCTATGGTAGTA | 56929 |
| rs568294823 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546128 | GTTGTTCAGAAGTTT[A/G]TGTAGTTTTGCATAA | 56929 |
| rs568729368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115531414 | TTCAGAAAACATTAT[A/G]TGCAGTAAAGTTTAA | 56929 |
| rs568904752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534478 | TTTTGAGTTTGATAA[A/G]GGCAAGTGATTGTTA | 56929 |
| rs569281649 | snp | C/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546424 | CCAGCATATGTCACA[C/G]TTCTATACTCTCCCA | 56929 |
| rs569382826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538427 | CATAGTGCTTGCCAT[C/T]AAGGAGCTTATAATC | 56929 |
| rs569491240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115531841 | GCTGGATTTGAACCC[C/T]GGGCCATAGTTTGCC | 56929 |
| rs569702571 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546319 | TTAAGGTAATTGCCA[C/G]TGAGAAGAAAATATA | 56929 |
| rs569735816 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545801 | CTTCTTCATATAGTA[A/G]TTGATAAACCTCTGG | 56929 |
| rs570013491 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538329 | TTCTACCTGTGCTAC[C/T]CATTTTTGTCCAACT | 56929 |
| rs570027446 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521774 | AGTATTTTATTATAA[G/T]CCATCTCATAATTGT | 56929 |
| rs570325783 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540542 | AAAGAGAGAACAGAC[A/G]TACCCTCACATATAA | 56929 |
| rs570370582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115536594 | AAACAACTTAGGGTA[C/T]CAAAGGAGCACTAGA | 56929 |
| rs570591315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115526473 | TGTTCTAACACTGTC[C/T]TTTTCTTCCCACACA | 56929 |
| rs570697934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541020 | AAGCCATGCTGTCAT[C/T]TGATCTACCAAGCCA | 56929 |
| rs570706444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115533747 | AACAATAAAACAACA[A/C]AAAGTTCAAAAATAA | 56929 |
| rs570941580 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540824 | ATGAGTTTATCAATA[A/G]TATCTACATCAAGCT | 56929 |
| rs571046554 | snp | C/T | | | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543655 | TTCCGTCCTACTGCT[C/T]TCCAACATCTGACAA | 56929 |
| rs571153322 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523656 | AAAATTGTCATGCTA[C/T]AGAGTACTTTCAAAA | 56929 |
| rs571259357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115527617 | CCCATGTTTTTCTAA[C/G]AAATAGGCAATATAA | 56929 |
| rs571323144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528103 | TTGAATACACCCACA[C/T]ACCAGGAGAAAAAAA | 56929 |
| rs571439323 | snp | A/G | | | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544152 | CAAACCCCGGCTAAG[A/G]CCAAAACTGTGCCCC | 56929 |
| rs571443612 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522650 | TGCATTGATGACTCC[C/T]TAAATAGTGTAACAT | 56929 |
| rs571571474 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532323 | TAAAGCTAAGGTAGA[G/T]TCTAAATTTTTAATA | 56929 |
| rs571623496 | snp | G/T | 0.000183039 | 0.00956483 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543433 | TGCTTGCCAACAATT[G/T]GGTGAGAAGCCGGAG | 56929 |
| rs571672816 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535771 | AGAAATGAAAACATA[G/T]ATCCACAGAAGAATT | 56929 |
| rs571797109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542551 | ATAGTAATTTCTACT[A/C]CAAGGTTGTTCTAAA | 56929 |
| rs571846989 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523278 | TTTAGCTCTTTTTGT[A/G]ACTAAAAGTGATTTG | 56929 |
| rs572021992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530781 | TCGGTCAAAGAAGCA[A/C]GCCCAATGAAAATCA | 56929 |
| rs572211441 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115537817 | AGTCAAGAAGGAAAA[C/G]AGAACTTCAGCTTTC | 56929 |
| rs572623254 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521220 | TGTCATTATCTCATC[C/T]AGCCTGCACAATTCT | 56929 |
| rs572752509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115528467 | ATTCCCCACACTTTG[G/T]GTTAAACCTCCAACT | 56929 |
| rs572997659 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545006 | GAGGGGGCGGATCTG[C/T]GCCCATCGAAGCGGC | 56929 |
| rs573042391 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | FEM1C | GRCh38.p7 | 5:115530202 | AAGTGAAAGTTTGGG[-/A]AAAAAAATGCCCTTT | 56929 |
| rs573234640 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524080 | GACAATTTTAGAAAT[C/T]TGAATGTTACATTTC | 56929 |
| rs573241055 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546690 | TGAACCCAAGAGGTC[A/G]AGACCAGCCTGGACA | 56929 |
| rs573252625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540496 | AGATACTGATACTGG[A/G]GAAAAAAATGACTTA | 56929 |
| rs573287722 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540059 | TCCTAAGGAATTATT[C/G]TAATTTAACTCTAGT | 56929 |
| rs573300423 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523226 | ATTATCCTAGATGCC[C/T]AGATCTGGCTTGGCA | 56929 |
| rs573399403 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FEM1C | GRCh38.p7 | 5:115533084 | AACGCCTACCTAAAA[C/T]AGAATCACAAATGTG | 56929 |
| rs573480378 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544706 | CGCCACGCCCCGCCA[C/G]CCGAGCTGCCTCCCG | 56929 |
| rs573622248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115536862 | TCTGCATCCAAAGAG[A/G]TAAGATGCATTCTTA | 56929 |
| rs573637951 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115520943 | ATTAAACCTTACAAT[A/G]AATGTTGTGGCATAT | 56929 |
| rs573720512 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526754 | GACCTTCTTGCAAGG[C/T]TGGACCTTTGGCTGG | 56929 |
| rs574059598 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538443 | AAGGAGCTTATAATC[C/T]TTCCTCTCTTAAATC | 56929 |
| rs574254101 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FEM1C | GRCh38.p7 | 5:115534899 | AGAGAAGGATTCTTA[A/T]TTTCTTGTTTGCTAT | 56929 |
| rs574259657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534141 | GAAAATCTGGAAGAA[C/T]GAAAAGTGCCATTTT | 56929 |
| rs574627027 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FEM1C | GRCh38.p7 | 5:115530401 | TACGTAAAGTAAAAA[G/T]CGACAGAACTACTAG | 56929 |
| rs574867251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115538712 | GTACCTAGATTAAAT[C/G]TCCTTTAAAATTCAG | 56929 |
| rs575013767 | in-del | -/AG | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545566 | TCGTAATTACACCTC[-/AG]AACACACACGGAGGA | 56929 |
| rs575188037 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528366 | CTGGAAGAGCTAGCT[C/G]AAACACTGAGCAGAA | 56929 |
| rs575293524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115543693 | ACCAAACTAGAGAAA[A/G]AAAAAAAAAGTAGCA | 56929 |
| rs575295380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115535011 | CAGCCCTGTTTTACA[C/G]CATATAGAAATAAAA | 56929 |
| rs575356388 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538990 | CGCTCTAAAATCCTA[C/T]AGCATGGATTGCTTA | 56929 |
| rs575414725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115541378 | GATCTTGTATCATTT[C/T]TATAAAAGATCACAC | 56929 |
| rs575457846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542887 | ACCAGTGCTTATAAT[A/G]ATGTATCAAACTTCC | 56929 |
| rs575506738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115525787 | CAGTACCTAAAACTA[G/T]TATCTGATATTAAAC | 56929 |
| rs575578374 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115540595 | TAAAGGGAACATTGT[A/T]TTGAAAGAGCTCAAA | 56929 |
| rs575736010 | snp | A/C/G | 3.39716e-05 | 0.00412127 | missense | FEM1C | GRCh38.p7 | 5:115524838 | GCAAAATAATAGAAA[A/C/G]GGCCTTATTTAACTG | 56929 |
| rs575773878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115530129 | AAGATACAAAGAAAA[C/T]TCAAGACACACTGCC | 56929 |
| rs575817081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537748 | CCTTCCCCCTTTTAT[G/T]TTTCTCTGTAAGTAG | 56929 |
| rs575946515 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522368 | ATTCTTAATATATGT[A/G]ACAGTTCAAATATTT | 56929 |
| rs575977008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115537024 | GACAGAAAACTTCAA[A/C]ATTATAATTCCCTGT | 56929 |
| rs576097742 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521478 | TGTCAGATTTATGAA[C/T]AAGAAAAATGACTAT | 56929 |
| rs576218324 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544861 | CCGGGGGAGGGCGGC[A/G]GCCGCGGCCAGCAAC | 56929 |
| rs576330997 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545518 | GGACTAGTCTTCCGT[A/C]CTTACTTTGGTGGGC | 56929 |
| rs576525097 | snp | A/T | 0.0138799 | 0.0821421 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523142 | AGGTATACATAAGCT[A/T]GAAGAAAGAAAGAAC | 56929 |
| rs576593633 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520741 | AAAAAAATTTAGAAT[A/G]AACTGTACATAAATC | 56929 |
| rs576654100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115527318 | TAAAGTTAGAAAAAA[A/G]CAAGTTATTATAAGA | 56929 |
| rs576767113 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533651 | AAAAACATTCCCATA[A/G]TACAGCGATCGTACT | 56929 |
| rs576780364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115535770 | GAGAAATGAAAACAT[A/C]TATCCACAGAAGAAT | 56929 |
| rs577167023 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532371 | TAATTCAATCTTAGC[G/T]TTTGCAGACAAAATA | 56929 |
| rs577249204 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523974 | TATAAAATTCACAAA[C/G]CAGTAAAGTATAAAG | 56929 |
| rs577275505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115531031 | TTTAACTGTTGCCCC[C/T]TTTTAATCTTATATT | 56929 |
| rs577315333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115539752 | ATCAAGGACTGGCTA[C/T]CTTGTCTTATTGCTC | 56929 |
| rs577626335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FEM1C | GRCh38.p7 | 5:115543864 | TACAGAAGGATACAC[A/G]GAGACCCAAATGTTC | 56929 |
| rs577674812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FEM1C | GRCh38.p7 | 5:115527817 | ACCATCTTGGCCAAC[A/G]TGGTAAAACCTTGTC | 56929 |
| rs577688189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115534606 | CTAAACCACCCTCAC[A/G]GAGTAGACAGAATTT | 56929 |
| rs577694474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115525937 | TATTATCTAAAAATC[A/G]GTAGAATACAAATAA | 56929 |
| rs577714034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115536002 | CATTTAAATTAAATG[G/T]CCAGAACAGGCAAAC | 56929 |
| rs577716551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544453 | CCGGCGCCCTCCTTC[C/T]CGCCCAGGCCTTCCG | 56929 |
| rs577850427 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545666 | CTAAAAAGCATAAAG[A/G]CTACGAGGAATGGTA | 56929 |
| rs577918319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115533115 | TGATGGCTTAATAGA[A/C]ATCTTCAATTCACTA | 56929 |
| rs577952492 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529960 | ACAAATAAAAATCAG[A/G]AAAGTACCCAGGAGA | 56929 |
| rs578220467 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527109 | CAAAGATTTCTCTAC[A/G]CTTCACCTGCGGCTT | 56929 |
| rs578262482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FEM1C | GRCh38.p7 | 5:115542015 | TTTTTTTTAACATGT[C/T]TATATGCTACTTTTA | 56929 |
| rs745343643 | snp | C/G/T | 3.32095e-05 | 0.00407478 | missense | FEM1C | GRCh38.p7 | 5:115524550 | TGTCTGGATGGTTGT[C/G/T]AAGAGCAGCGATATG | 56929 |
| rs745689067 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541283 | TTCAGAAATATCTTT[C/G]GAAGTATTATCCCTG | 56929 |
| rs745787359 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543095 | GTGTTCTACAAGGTA[C/T]TTCACTATTTCCAAA | 56929 |
| rs745805350 | snp | C/T | 1.65184e-05 | 0.00287384 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543281 | AAAATTGACGGAGCC[C/T]CCAACTTCTATGGAG | 56929 |
| rs745989066 | snp | G/T | 1.70211e-05 | 0.00291724 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543460 | GGAGTTTGCCATCCC[G/T]AGCTGCGTTAAATAC | 56929 |
| rs746234339 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534798 | AAATCACCAGAGAAT[A/C]ATAATAAAATGCAGA | 56929 |
| rs746246735 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533655 | ACATTCCCATAATAC[A/G]GCGATCGTACTTCCC | 56929 |
| rs746308889 | snp | A/C | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115520934 | TTTAATTTTATTAAA[A/C]CTTACAATGAATGTT | 56929 |
| rs746363142 | snp | C/T | 1.65211e-05 | 0.00287407 | missense | FEM1C | GRCh38.p7 | 5:115525533 | ATTCCATAACCATCC[C/T]TTTCCATCTTGGCAC | 56929 |
| rs746489902 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543083 | CAAATCAGCTTTGTG[G/T]TCTACAAGGTACTTC | 56929 |
| rs746490628 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530767 | ACTCACTTGCTTCGT[C/T]GGTCAAAGAAGCAAG | 56929 |
| rs746508895 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546212 | ACGTTTCTTATGTTT[C/T]TACAGTCTTAATAAT | 56929 |
| rs746631310 | snp | C/T | 1.66018e-05 | 0.00288108 | missense | FEM1C | GRCh38.p7 | 5:115524372 | TTATAATATATTCTA[C/T]GATTCACTATGACAC | 56929 |
| rs746647172 | in-del | -/TA | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521760 | TAACACAAATTTAAG[-/TA]TATTTTATTATAATC | 56929 |
| rs746807073 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538861 | TCCACAGATCCACAT[C/G]CCAATAAACTTTCTG | 56929 |
| rs746927478 | in-del | -/TC | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520664 | ATTAAAGGCATCCCT[-/TC]TCTCATGCAGTTGAC | 56929 |
| rs746936290 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540035 | TTCCAGTGAATGACA[C/T]ACAAAATGTCCTAAG | 56929 |
| rs746936297 | snp | C/G | 1.77065e-05 | 0.00297539 | intron-variant | FEM1C | GRCh38.p7 | 5:115542904 | TGTATCAAACTTCCT[C/G]AAAATAAGTGGTAGA | 56929 |
| rs747181731 | snp | A/C | 1.64863e-05 | 0.00287104 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543332 | GAATTCCACCATGTC[A/C]AGGTGCCCATACCTG | 56929 |
| rs747194671 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536949 | TTTCAAGGCTAAGAG[C/T]ACTGGAGCTAAGGGA | 56929 |
| rs747273097 | snp | A/C | 1.67273e-05 | 0.00289195 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543443 | CAATTTGGTGAGAAG[A/C]CGGAGTTTGCCATCC | 56929 |
| rs747614347 | snp | A/G | 1.68775e-05 | 0.0029049 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525606 | CTGCACAATCATGCA[A/G]TGCAGTATTACCTTA | 56929 |
| rs747695868 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531848 | TTGAACCCTGGGCCA[C/T]AGTTTGCCAAACCTG | 56929 |
| rs747756012 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530977 | TGAAAAAAGGGATAC[G/T]TATGCGAATACAGCA | 56929 |
| rs747882478 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541409 | TTGTATCATTTTTAT[A/G]AAAGATCACACAATC | 56929 |
| rs747924343 | snp | C/T | 3.59105e-05 | 0.00423721 | missense | FEM1C | GRCh38.p7 | 5:115524666 | TTACAAACAGGGTAC[C/T]GCCCTACACATGTAG | 56929 |
| rs747961425 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115525834 | ATGACCAAATTAGGT[A/G]TAAAAAGACATCCAA | 56929 |
| rs748016874 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540261 | GAAGCTTCAGGATCA[C/G]AGTGGAGGAGGATGA | 56929 |
| rs748040166 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527200 | GTACAGTTATATGGT[C/G]AGTTACTTCCAAATT | 56929 |
| rs748079871 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528160 | GAAGACTTTCACATC[A/C]AGTAATGGCAGAGAT | 56929 |
| rs748124000 | snp | A/G | 1.64985e-05 | 0.0028721 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525160 | GTAAGAGGTATCAGG[A/G]TGAGAAGGACCAAGA | 56929 |
| rs748234089 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537689 | TAAGTTATTTAAACA[C/T]TACTCAATCAAAATA | 56929 |
| rs748255560 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537040 | ATTATAATTCCCTGT[C/T]CTCTAGTTCACAGAC | 56929 |
| rs748264726 | in-del | -/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542578 | TAAAAAAAAAAAAAA[-/C]AAAACAAAAAGCTAA | 56929 |
| rs748330480 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538524 | CATGGGGTAAAAACA[C/T]TAGGTCTTTAGCCTC | 56929 |
| rs748396145 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521544 | GACTGGCATCTAAGT[A/G]AAATGACCATTTCTT | 56929 |
| rs748429947 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534641 | CTCTTTATAAAAAAA[C/T]AAAAATGTCCTCCTA | 56929 |
| rs748468773 | snp | A/G | 1.66471e-05 | 0.00288501 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524350 | TAGCTTTTCTGGGAT[A/G]TGCCCTTTATAATAT | 56929 |
| rs748509761 | snp | G/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545346 | ACAATCAGCTCTCCT[G/T]AGACGTACTCACTAC | 56929 |
| rs748705585 | snp | C/T | 6.60829e-05 | 0.00574779 | missense | FEM1C | GRCh38.p7 | 5:115525024 | ATAATAAGCTGCTGG[C/T]GGTCATTGGGCTTAA | 56929 |
| rs748896415 | snp | A/T | 1.65734e-05 | 0.00287862 | missense | FEM1C | GRCh38.p7 | 5:115525566 | TACATAAGAAGCATC[A/T]TCATGATGTCCAAAC | 56929 |
| rs749045602 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546612 | GTTTAAAGGCTACCA[A/G]TTTCTGCTGTGGCTC | 56929 |
| rs749084121 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528595 | AGGATGACTAGTATA[C/T]AGAATTAAAAGCCAG | 56929 |
| rs749208562 | snp | A/C | 1.66272e-05 | 0.00288328 | missense | FEM1C | GRCh38.p7 | 5:115524559 | GGTTGTTAAGAGCAG[A/C]GATATGCAGGGGACT | 56929 |
| rs749212249 | snp | A/C | 1.65971e-05 | 0.00288067 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543424 | CTTTGGATTTGCTTG[A/C]CAACAATTTGGTGAG | 56929 |
| rs749270892 | in-del | -/AAG | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535585 | ATGGCTATATTAAAA[-/AAG]AAGAAGAAGAAGAAC | 56929 |
| rs749318196 | snp | C/G | 1.66474e-05 | 0.00288503 | missense | FEM1C | GRCh38.p7 | 5:115524860 | ATTTAACTGTAATGG[C/G]TCAGCTGGACACTGA | 56929 |
| rs749480301 | snp | C/T | | | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525289 | ATAAGCCATTATTAG[C/T]GTCTGTGGCACTGGT | 56929 |
| rs749609128 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532065 | GTCCTTCAAATCTCA[C/T]TAGAAATTTCAACTG | 56929 |
| rs749662260 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546553 | CATCTTCAAACTGAG[C/T]TCTGTATCCCTCATG | 56929 |
| rs749862912 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536607 | TATCAAAGGAGCACT[A/G]GAAGAAGGATTCTCT | 56929 |
| rs750100068 | snp | C/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523843 | GGTTTGTACAACCTA[C/G]TATGGGTCCATAAGG | 56929 |
| rs750370035 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530547 | AATAAAAGAACATGG[C/T]ACTCAACAACCATAG | 56929 |
| rs750457312 | snp | G/T | 1.65375e-05 | 0.0028755 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115542975 | TTTTCTATTAACATC[G/T]GCCCCCTTTTCAAGT | 56929 |
| rs750554819 | snp | C/T | 1.75118e-05 | 0.00295898 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524295 | TTAACAGTGCTAAAA[C/T]ACAGTCAAGTTATCA | 56929 |
| rs750738638 | in-del | -/TACTC | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546189 | TGCTTTTCCTTTCTA[-/TACTC]TAAACGTTTCTTATG | 56929 |
| rs750912554 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537692 | GTTATTTAAACATTA[C/T]TCAATCAAAATAAAT | 56929 |
| rs750957427 | snp | C/G | 1.87071e-05 | 0.0030583 | intron-variant | FEM1C | GRCh38.p7 | 5:115525647 | GAAAAAAAGAAATAA[C/G]ATACATTGAGGGACC | 56929 |
| rs750973170 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536645 | ATGTTTCCCTTCCCC[A/G]TGTGTAGTCTATCAT | 56929 |
| rs751119116 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536085 | AATGAGGAGGGATAG[A/G]AGGGAGTGACTCTTA | 56929 |
| rs751124842 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532785 | GCAAGGGAGCAAGTC[A/T]TACATTACATAAACA | 56929 |
| rs751149775 | snp | A/G/T | 9.91533e-05 | 0.00704049 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543275 | GCCATCAAAATTGAC[A/G/T]GAGCCCCCAACTTCT | 56929 |
| rs751269380 | snp | C/T | 1.65858e-05 | 0.00287969 | missense | FEM1C | GRCh38.p7 | 5:115524532 | TAATAAGGAGATTCA[C/T]GATGTCTGGATGGTT | 56929 |
| rs751294019 | snp | C/T | 1.65362e-05 | 0.00287538 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543403 | AGATCAAGGAGGAAA[C/T]CTCCTCTTTGGATTT | 56929 |
| rs751301224 | in-del | -/A | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521079 | GTGACACATAAGGGC[-/A]AAAAAAAAAAAAAGA | 56929 |
| rs751315990 | snp | C/G/T | 9.93368e-05 | 0.00704695 | missense | FEM1C | GRCh38.p7 | 5:115524949 | CATCAAATGTAACAG[C/G/T]AGTACCCAGCAGGCC | 56929 |
| rs751347260 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534045 | ATTAATTCTGTTAAA[A/G]CATTTCTCTAGAAAG | 56929 |
| rs751365424 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527728 | CAAAAGCTGGCCAGG[A/C]GCGGTAGCTCACGCC | 56929 |
| rs751476010 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541250 | TATAAAACTGCATAC[A/G]TATATCAGTATGCAA | 56929 |
| rs751477549 | snp | C/T | 3.30011e-05 | 0.00406195 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525082 | CAAAGCATACTTCCA[C/T]AGGTTGATGCATCGT | 56929 |
| rs751555170 | snp | A/T | 3.2994e-05 | 0.00406152 | missense | FEM1C | GRCh38.p7 | 5:115525227 | TCATCAGGATCAGCA[A/T]TAAGACCTTCTAGCT | 56929 |
| rs751593649 | snp | A/G | | | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544208 | ACTCACGGCTCTCAG[A/G]AAATCCGCCTGCCTT | 56929 |
| rs751643044 | snp | C/T | 1.65075e-05 | 0.00287289 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525493 | ATTTGTGTGACCAGT[C/T]ACACTTGCTGAGAGA | 56929 |
| rs751800876 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115525642 | AGAGAGAAAAAAAGA[A/C]ATAACATACATTGAG | 56929 |
| rs751873088 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531297 | TTTCACAATTTCTCT[A/G]AGGAAAAGCAGACAA | 56929 |
| rs751885318 | snp | C/T | 1.73087e-05 | 0.00294177 | missense | FEM1C | GRCh38.p7 | 5:115524617 | ATCAGCACCACATTC[C/T]ATCAGTATTGCAGTA | 56929 |
| rs751959345 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538084 | TGCTTTAAACTACTA[C/T]AGAAAACAAAAGGAA | 56929 |