| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs752080627 | snp | A/G | 1.65086e-05 | 0.00287298 | stop-gained | FEM1C | GRCh38.p7 | 5:115525057 | GATCCAAATTGCTCT[A/G]CTGCATATCCAAAGC | 56929 |
| rs752112976 | in-del | -/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532538 | AGCTTAGAAAACAGA[-/G]GGGAAAAAAAAAAGG | 56929 |
| rs752266267 | in-del | -/TT | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535688 | TGCTTTGAAAAACAG[-/TT]TTTAACGGTTCCTGT | 56929 |
| rs752294271 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536015 | TGTCCAGAACAGGCA[A/C]ACTTAAGACAGAAAA | 56929 |
| rs752349440 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534285 | GTTAATTTTAAAGAC[A/G]CCTGTAATCTTTTAA | 56929 |
| rs752355409 | snp | A/T | 4.94205e-05 | 0.0049707 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543050 | CAAGCACGTATGCCC[A/T]TGTCGGTTTGACACT | 56929 |
| rs752462614 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533321 | ATCTGGCTTTCTATG[C/T]ATAAGCACTTTATAA | 56929 |
| rs752921184 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539764 | CTATCTTGTCTTATT[A/G]CTCTTTGTATATCCT | 56929 |
| rs752925256 | snp | A/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523032 | AGCTAACTTCCAGTA[A/T]GGGAACAGGAAGCAC | 56929 |
| rs752932852 | snp | C/T | 1.65061e-05 | 0.00287277 | missense | FEM1C | GRCh38.p7 | 5:115525477 | TCAGAAAATCCACAA[C/T]ATTTGTGTGACCAGT | 56929 |
| rs752945818 | snp | A/G | 1.64958e-05 | 0.00287187 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525274 | TTCCTTGGCATAATC[A/G]TAAGCCATTATTAGT | 56929 |
| rs752977913 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540771 | CTCATCTCTCCAATA[A/T]CATAGGCTTTTAAAA | 56929 |
| rs753013890 | snp | A/T | 3.30409e-05 | 0.0040644 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543263 | CTCAATGGTTTCGCC[A/T]TCAAAATTGACGGAG | 56929 |
| rs753154812 | in-del | -/CACT | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540405 | TGGGTATAAAGTTGA[-/CACT]GGTTACGAGAAAACA | 56929 |
| rs753177422 | snp | A/G | 0.000182302 | 0.00954556 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524487 | CAGTTTGTTTGTGCA[A/G]GTTTGTGGCATCAAA | 56929 |
| rs753214998 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526817 | ATACTGATCTAAAAC[C/T]TTCCCTAAATGATAA | 56929 |
| rs753244780 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115543753 | ACACTTCTTAATTTC[C/T]ACTTCTGTGGGAAGA | 56929 |
| rs753269080 | snp | G/T | 1.68704e-05 | 0.00290429 | missense | FEM1C | GRCh38.p7 | 5:115524590 | GTTGTCATCCGAGTC[G/T]CTGACGTTCACATCA | 56929 |
| rs753300328 | in-del | -/ATAAC | 1.84213e-05 | 0.00303485 | intron-variant | FEM1C | GRCh38.p7 | 5:115525643 | GAGAGAAAAAAAGAA[-/ATAAC]ATACATTGAGGGACC | 56929 |
| rs753336652 | snp | C/G | 1.80589e-05 | 0.00300485 | missense | FEM1C | GRCh38.p7 | 5:115524778 | GCTTTTTGAAATGGT[C/G]TTGTTCTAGAGTACA | 56929 |
| rs753405581 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530753 | TTTGAATTTTTAATA[C/T]TCACTTGCTTCGTCG | 56929 |
| rs753428967 | snp | C/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522616 | GACTAAAGATGATGA[C/G]ATACCTAATGTGACT | 56929 |
| rs754039244 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526893 | ATGCTGAATGTCTGG[A/T]TTCCTTCTGGGAGTC | 56929 |
| rs754067589 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540791 | GGCTTTTAAAACATA[C/T]CCCAATTTGACTTAA | 56929 |
| rs754124488 | snp | G/T | 1.64999e-05 | 0.00287222 | missense | FEM1C | GRCh38.p7 | 5:115525098 | AGGTTGATGCATCGT[G/T]TGAAATTTCCAGAGT | 56929 |
| rs754180099 | snp | A/G | 4.66646e-05 | 0.00483013 | intron-variant | FEM1C | GRCh38.p7 | 5:115525666 | CATTGAGGGACCAAA[A/G]TATAATGTAATATAT | 56929 |
| rs754203372 | in-del | -/AGTC | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546777 | CACACACAAAAAATT[-/AGTC]AGGCATGGCATGCAG | 56929 |
| rs754263321 | in-del | -/AAATAGCTAA | 3.54541e-05 | 0.0042102 | frameshift-variant | FEM1C | GRCh38.p7 | 5:115524646 | AACTTGTAGAGATGG[-/AAATAGCTAA]AAATTTACAAACAGG | 56929 |
| rs754552202 | snp | C/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546240 | AATTTTTAAGTATAG[C/G]ATAGTATTTCCCTTA | 56929 |
| rs754571909 | snp | A/G | 4.97137e-05 | 0.00498542 | missense | FEM1C | GRCh38.p7 | 5:115524916 | CAAGGACGCTTTTGC[A/G]AAGTATGCCCATAAG | 56929 |
| rs754652651 | snp | C/T | 2.32415e-05 | 0.00340884 | intron-variant | FEM1C | GRCh38.p7 | 5:115525667 | ATTGAGGGACCAAAA[C/T]ATAATGTAATATATA | 56929 |
| rs754766480 | snp | C/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546665 | CGGAGGCTGAGACAG[C/G]CAGATTGCTTGAACC | 56929 |
| rs754983785 | snp | C/T | 1.80471e-05 | 0.00300387 | missense | FEM1C | GRCh38.p7 | 5:115524780 | TTTTTGAAATGGTCT[C/T]GTTCTAGAGTACAAG | 56929 |
| rs755085545 | snp | A/G | 3.29984e-05 | 0.00406179 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525121 | TCCAGAGTCTGCATA[A/G]ACAGCGCCTCTATAT | 56929 |
| rs755141551 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530283 | CTTTAATGCAAAATA[A/C]ATAATTAGTGAAAAA | 56929 |
| rs755247257 | snp | G/T | 3.4873e-05 | 0.00417556 | missense | FEM1C | GRCh38.p7 | 5:115524821 | TAACAAGCAAATTAA[G/T]TGCAAAATAATAGAA | 56929 |
| rs755272956 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540211 | ACCATTAACCCATAG[-/A]AAAAAAATCCAGAAC | 56929 |
| rs755337291 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523054 | AGGAAGCACTGCAAC[C/T]TTTCATGTTTAACTG | 56929 |
| rs755388263 | in-del | -/A | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545860 | AAACTAGGATGAAAA[-/A]GTTTAAATGTGTTTG | 56929 |
| rs755455847 | in-del | -/GTTT | 1.66015e-05 | 0.00288105 | frameshift-variant | FEM1C | GRCh38.p7 | 5:115524876 | TCAGCTGGACACTGA[-/GTTT]GTTTGATAGCTCGCT | 56929 |
| rs755467025 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536712 | AATTAAAAAAAAGAA[A/G]ATAAATTGTGCCAAG | 56929 |
| rs755500670 | snp | C/T | 1.6722e-05 | 0.00289149 | missense | FEM1C | GRCh38.p7 | 5:115524331 | GAAGGGAAACAAAAG[C/T]CTCTAGCTTTTCTGG | 56929 |
| rs755560748 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534407 | CCAAAAACATAGCTG[C/T]ATTTTGAGGAAGAAC | 56929 |
| rs755575242 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523961 | AGACTTTCAATTGTA[C/T]AAAATTCACAAACCA | 56929 |
| rs755693706 | snp | A/G | 1.7565e-05 | 0.00296347 | missense | FEM1C | GRCh38.p7 | 5:115524633 | ATCAGTATTGCAGTA[A/G]CTTGTAGAGATGGAA | 56929 |
| rs755817799 | snp | C/T | 5.42883e-05 | 0.00520972 | missense | FEM1C | GRCh38.p7 | 5:115524757 | TAAGAAACCTGTATA[C/T]AGTCTGCTTTTTGAA | 56929 |
| rs755922288 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542854 | CAAAACAGGTCTGTC[A/G]ATGCTGGTTTACTCA | 56929 |
| rs755965045 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528001 | GAGACTTCGTCTCAG[-/A]AAAAAAAAAAAAAAA | 56929 |
| rs755975089 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528493 | CAACTTTAACCCTAG[A/G]GAGTTAAAGTTAACT | 56929 |
| rs756055377 | snp | A/G | 1.65154e-05 | 0.00287358 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543285 | TTGACGGAGCCCCCA[A/G]CTTCTATGGAGGCAC | 56929 |
| rs756076689 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530623 | GACCATATTCTTGGC[A/C]GTAAGGCAAGTCTCA | 56929 |
| rs756167152 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538557 | AGACTATGTAGTAGA[A/G]TGCGGTTAGATGTCA | 56929 |
| rs756253538 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535376 | ATATAAACAACTCTT[-/A]ACAGTTCAGTAATAC | 56929 |
| rs756257363 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539875 | CAAAATGCCAATAGC[C/T]TGTTAAAAAGTAATG | 56929 |
| rs756315562 | snp | C/T | 1.7011e-05 | 0.00291637 | stop-lost | FEM1C | GRCh38.p7 | 5:115524308 | AATACAGTCAAGTTA[C/T]CATCTATGAAGGGAA | 56929 |
| rs756438799 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526834 | TCCCTAAATGATAAG[A/G]GTATCTCACTGTACC | 56929 |
| rs756496700 | snp | A/C | 3.31395e-05 | 0.00407046 | missense | FEM1C | GRCh38.p7 | 5:115524924 | CTTTTGCAAAGTATG[A/C]CCATAAGATCATCAA | 56929 |
| rs756771329 | in-del | -/AAG | 3.48967e-05 | 0.00417698 | intron-variant | FEM1C | GRCh38.p7 | 5:115542934 | ACATTTAGAAAAACA[-/AAG]AAGCTGAACTCACCT | 56929 |
| rs756778416 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536223 | TTTTGTGAATTTTAT[C/T]TCAATAAGGCTGTTT | 56929 |
| rs756842783 | in-del | -/TAG | | | cds-indel | FEM1C | GRCh38.p7 | 5:115521353 | AATTTTCCCAAATAA[-/TAG]TAGACTGGGGTCTCT | 56929 |
| rs756853646 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539922 | CATGTTCAAATATCA[A/G]CCGCCTGTTTAAAAG | 56929 |
| rs756875530 | snp | C/G | 1.6588e-05 | 0.00287988 | missense | FEM1C | GRCh38.p7 | 5:115524536 | AAGGAGATTCATGAT[C/G]TCTGGATGGTTGTTA | 56929 |
| rs756947858 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545739 | GCTCTGAGTAATAAA[C/T]CGGGAACTAAAGCTT | 56929 |
| rs757057166 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530451 | AACATTAGTACATCT[A/T]AACATATCTTTCTCA | 56929 |
| rs757085338 | snp | C/T | 1.65002e-05 | 0.00287225 | missense | FEM1C | GRCh38.p7 | 5:115525090 | ACTTCCATAGGTTGA[C/T]GCATCGTTTGAAATT | 56929 |
| rs757296307 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531449 | GGATATTCAAGGATA[C/T]GTATTTTAAAAGACT | 56929 |
| rs757319517 | snp | C/T | | | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544228 | CCGCCTGCCTTTTAG[C/T]CATTAACTTCGCCCG | 56929 |
| rs757329284 | snp | A/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546013 | TATTACAGTAGGCAG[A/T]CTGACCCTCAGCATA | 56929 |
| rs757782894 | snp | C/G | 1.64942e-05 | 0.00287173 | missense | FEM1C | GRCh38.p7 | 5:115525294 | CCATTATTAGTGTCT[C/G]TGGCACTGGTTTACT | 56929 |
| rs757799857 | snp | C/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545033 | CGGCCCGAGGCAGCT[C/G]GAGTTCTGAGATCTC | 56929 |
| rs757870961 | snp | C/T | 1.65067e-05 | 0.00287282 | missense | FEM1C | GRCh38.p7 | 5:115525495 | TTGTGTGACCAGTCA[C/T]ACTTGCTGAGAGAAG | 56929 |
| rs757893998 | snp | A/C | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522884 | TTTTAGTACTTTTCA[A/C]TTATCTTAAGTTAAA | 56929 |
| rs757991027 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543062 | CCCATGTCGGTTTGA[C/T]ACTTCCAAATCAGCT | 56929 |
| rs758175942 | snp | A/C | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523100 | GAGACCAAAGTAATC[A/C]AAGTAATTCATGCAA | 56929 |
| rs758274405 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531713 | CTTTTACTTTTGTAC[A/T]CTAAAATTTGATTTT | 56929 |
| rs758278400 | snp | A/G | 1.72573e-05 | 0.00293741 | missense | FEM1C | GRCh38.p7 | 5:115524828 | CAAATTAAGTGCAAA[A/G]TAATAGAAAGGGCCT | 56929 |
| rs758412785 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523932 | TGAGAAGAGAAGAAA[A/G]AAGCAAGAAAAAAAG | 56929 |
| rs758468709 | snp | C/T | 1.64953e-05 | 0.00287182 | missense | FEM1C | GRCh38.p7 | 5:115525285 | AATCATAAGCCATTA[C/T]TAGTGTCTGTGGCAC | 56929 |
| rs758530833 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527120 | CTACACTTCACCTGC[A/G]GCTTTACCCCTCATA | 56929 |
| rs758582155 | snp | G/T | 1.65072e-05 | 0.00287286 | missense | FEM1C | GRCh38.p7 | 5:115525479 | AGAAAATCCACAATA[G/T]TTGTGTGACCAGTCA | 56929 |
| rs758698634 | snp | C/T | | | missense | FEM1C | GRCh38.p7 | 5:115524588 | CTGTTGTCATCCGAG[C/T]CTCTGACGTTCACAT | 56929 |
| rs758779860 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536665 | TAGTCTATCATGAGA[A/G]ATACTCAAGAACAGA | 56929 |
| rs758799177 | in-del | -/GAGA | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522943 | TGTGAGTGAGTGAGT[-/GAGA]GAGAGAGAGAGAGAG | 56929 |
| rs758800000 | snp | C/T | 1.65811e-05 | 0.00287929 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524506 | TGTGGCATCAAAATG[C/T]GCACCTGATTTAATA | 56929 |
| rs758827457 | snp | A/G | | | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543998 | TTGCACACGCCCAGG[A/G]AGAGTACAACCGAAA | 56929 |
| rs758900211 | in-del | -/TCTC | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538178 | AGTGGTTCAATGTAT[-/TCTC]TCTGTGTAAGTTAGA | 56929 |
| rs759007567 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537880 | AACCTAGAATGACAT[A/C]AATCATTATCTTAGT | 56929 |
| rs759133318 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542041 | TTTTAAATTTTAATG[C/G]CTTTTAAAAATTAGG | 56929 |
| rs759169069 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526682 | AACAGTCAGTCATTT[G/T]AGGCATGTCTGTAGA | 56929 |
| rs759241388 | snp | A/C | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521170 | AATGGTTAAAGTTCT[A/C]GGCAATAATGCTGCT | 56929 |
| rs759247638 | snp | C/T | 1.65094e-05 | 0.00287305 | missense | FEM1C | GRCh38.p7 | 5:115525050 | CTTAAAGGATCCAAA[C/T]TGCTCTGCTGCATAT | 56929 |
| rs759257753 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535750 | ACTCCTAGGTATGTG[C/T]CTGAGAGAAATGAAA | 56929 |
| rs759344199 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539002 | CTATAGCATGGATTG[C/T]TTATACTATTCCTTC | 56929 |
| rs759444395 | snp | C/T | 3.51587e-05 | 0.00419262 | intron-variant | FEM1C | GRCh38.p7 | 5:115542924 | TAAGTGGTAGACATT[C/T]AGAAAAACAAAGAAG | 56929 |
| rs759463788 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531360 | TGATTCTCAAAGCAC[C/T]ATCTGTGTGGAGAGA | 56929 |
| rs759488668 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537199 | ACATACATTCCTGCT[G/T]CCTCAACAGCATAAA | 56929 |
| rs759515936 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535217 | TATAAGTGACACATA[A/C]ATTTCCTTAAAAATC | 56929 |
| rs759565937 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526283 | TAGCCAAAATTCTTG[G/T]TAACAAAGGACTTTC | 56929 |
| rs759743607 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545608 | TCAGAAAATGTGATT[A/G]GTTTTGGAGGCTGTC | 56929 |
| rs759917670 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543002 | AAGTAAATACTGAGC[A/G]ATCTCTTTATGTCCT | 56929 |
| rs759973236 | snp | A/G | 8.25035e-05 | 0.00642222 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543227 | TCCTGCTGCAGAAGC[A/G]GCCCATAAAGGGGGA | 56929 |
| rs759988974 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540740 | TTTGGAAAATATAAC[A/G]GAAGTAATACCAGTT | 56929 |
| rs760057122 | in-del | -/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529863 | ATGCACATAACTACA[-/T]TTTTCTCTAACATAT | 56929 |
| rs760269756 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529395 | AAATGATATTTAAAA[C/G]CACGAAAGAAAAGTA | 56929 |
| rs760411709 | snp | C/T | 1.65842e-05 | 0.00287955 | missense | FEM1C | GRCh38.p7 | 5:115524896 | TTTGATAGCTCGCTC[C/T]ATTTCAAGGACGCTT | 56929 |
| rs760463403 | snp | A/C | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522130 | CCCTCCCACCCAGCC[A/C]CCAAAGAGGAGGAGG | 56929 |
| rs760492394 | in-del | -/A | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537525 | ATTTGCACACCATCT[-/A]CAGCTTAGTTTATCC | 56929 |
| rs760550060 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534931 | TAGATACTTGCCACA[C/T]AGCTAATATATCTAA | 56929 |
| rs760616653 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523617 | CAAAAAAGCTTGAGC[C/T]ATAATAGCTAACCTG | 56929 |
| rs760660472 | snp | A/G | 1.73712e-05 | 0.00294708 | intron-variant | FEM1C | GRCh38.p7 | 5:115525622 | TGCAGTATTACCTTA[A/G]AGAGAGAGAGAAAAA | 56929 |
| rs760824099 | snp | C/T | 1.67144e-05 | 0.00289084 | missense | FEM1C | GRCh38.p7 | 5:115524576 | ATATGCAGGGGACTG[C/T]TGTCATCCGAGTCTC | 56929 |
| rs760835940 | in-del | -/ATAC | 5.28267e-05 | 0.00513912 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524294 | TTTAACAGTGCTAAA[-/ATAC]AGTCAAGTTATCATC | 56929 |
| rs760845242 | snp | A/C | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543154 | GAGTTGAATTGGTTA[A/C]AGTCGTGTTGTTGAC | 56929 |
| rs760889899 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532509 | TAATTATAGCCTAGA[A/G]CATTATTACTTACAG | 56929 |
| rs760951465 | snp | A/T | 6.62295e-05 | 0.00575416 | missense | FEM1C | GRCh38.p7 | 5:115524469 | CATCCAGCAAGTCAC[A/T]AGCAGTTTGTTTGTG | 56929 |
| rs760966496 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542096 | AAATAGATTCGTGTA[A/C]GGGAAGTTAAGGTTT | 56929 |
| rs761106385 | snp | C/T | 3.30126e-05 | 0.00406266 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115542981 | ATTAACATCTGCCCC[C/T]TTTTCAAGTAAATAC | 56929 |
| rs761166342 | snp | C/G/T | 6.6067e-05 | 0.00574715 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525031 | GCTGCTGGCGGTCAT[C/G/T]GGGCTTAAAGGATCC | 56929 |
| rs761396571 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538997 | AAATCCTATAGCATG[A/G]ATTGCTTATACTATT | 56929 |
| rs761547477 | snp | A/G | 1.90627e-05 | 0.00308723 | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543535 | TATTTATCTTTCAAA[A/G]CAGAGCTCCAGTTTA | 56929 |
| rs761551819 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523798 | AAGATAAAGCACTTA[C/T]GGTAACTGCAAATGG | 56929 |
| rs761732928 | snp | C/T | 1.64982e-05 | 0.00287208 | missense | FEM1C | GRCh38.p7 | 5:115525237 | CAGCAATAAGACCTT[C/T]TAGCTCTTCTGCACT | 56929 |
| rs761749339 | snp | C/T | 1.65015e-05 | 0.00287237 | missense | FEM1C | GRCh38.p7 | 5:115525396 | CTCTTTTTTTGTCTA[C/T]AAATGTAGCTCCCAG | 56929 |
| rs761848205 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535395 | GTTCAGTAATACAAA[A/G]ATAACCCAGTTATAA | 56929 |
| rs761981563 | snp | C/T | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520482 | AGCCAATTCATTTTC[C/T]GACTCAACTAGAGCT | 56929 |
| rs762120949 | snp | A/G | 1.73393e-05 | 0.00294437 | intron-variant | FEM1C | GRCh38.p7 | 5:115542938 | TTAGAAAAACAAAGA[A/G]GCTGAACTCACCTTT | 56929 |
| rs762131030 | snp | C/G | 1.78768e-05 | 0.00298966 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524289 | CGTGCTTTAACAGTG[C/G]TAAAATACAGTCAAG | 56929 |
| rs762215975 | snp | C/T | | | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543648 | GAGTATGTTCCGTCC[C/T]ACTGCTTTCCAACAT | 56929 |
| rs762224568 | snp | A/T | 1.65869e-05 | 0.00287979 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524890 | AGTTTGTTTGATAGC[A/T]CGCTCTATTTCAAGG | 56929 |
| rs762288808 | snp | C/T | 1.8082e-05 | 0.00300677 | missense | FEM1C | GRCh38.p7 | 5:115524735 | TTCTTTCCCCTTGGA[C/T]GCAGCTTAAGAAACC | 56929 |
| rs762317807 | in-del | -/CTT | | | intron-variant | FEM1C | GRCh38.p7 | 5:115543741 | GAAGAAGGCAAAACA[-/CTT]CTTAATTTCCACTTC | 56929 |
| rs762322061 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530873 | GGCTTATTTTTTAAA[C/T]AGCTAAGTTTCCATC | 56929 |
| rs762341261 | in-del | -/AAC | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535297 | GTTAAAAAAAAAAAA[-/AAC]AAACACAGAATGAGA | 56929 |
| rs762484840 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540456 | TTCTCATGTTATATG[C/T]AGTTTTTTTAAAGAC | 56929 |
| rs762602437 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539474 | TTCTTAAATAGGAAC[A/C]AACTCCCGTCTCAAA | 56929 |
| rs762788715 | snp | C/T | 1.65416e-05 | 0.00287586 | missense | FEM1C | GRCh38.p7 | 5:115524451 | TTTTAGCTATTTCCT[C/T]CTCATCCAGCAAGTC | 56929 |
| rs762985396 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521892 | GCTATTAAATTAACT[A/G]GTTTTTCAAAACCTC | 56929 |
| rs763108157 | snp | A/C | 1.81777e-05 | 0.00301472 | intron-variant | FEM1C | GRCh38.p7 | 5:115525639 | GAGAGAGAGAAAAAA[A/C]GAAATAACATACATT | 56929 |
| rs763120813 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531951 | ATCCTAAGTACTTCT[C/G]CCAGCACCAAGAACA | 56929 |
| rs763266665 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545502 | ACACGTGAAGTCTCT[C/T]GGACTAGTCTTCCGT | 56929 |
| rs763366126 | snp | C/T | 1.65636e-05 | 0.00287776 | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543523 | GAGGCTGTGCTTTAT[C/T]TATCTTTCAAAGCAG | 56929 |
| rs763426702 | snp | C/T | 1.65018e-05 | 0.00287239 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543383 | GGCCCCATTTGTTTT[C/T]TCAGAGATCAAGGAG | 56929 |
| rs763454624 | snp | A/G | 1.80673e-05 | 0.00300555 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524716 | ATGAAGAGGGCTGAA[A/G]TTATTCTTTCCCCTT | 56929 |
| rs763637316 | snp | A/C | 3.29935e-05 | 0.00406149 | missense | FEM1C | GRCh38.p7 | 5:115525226 | CTCATCAGGATCAGC[A/C]ATAAGACCTTCTAGC | 56929 |
| rs763726005 | snp | A/C | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520649 | AATTAAAAAACAAAA[A/C]TTAAAGGCATCCCTT | 56929 |
| rs763792735 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537367 | CTATCTTAAGCTCAT[A/G]TTACTGCCACGAACA | 56929 |
| rs763849167 | snp | C/T | 1.65296e-05 | 0.00287481 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543274 | CGCCATCAAAATTGA[C/T]GGAGCCCCCAACTTC | 56929 |
| rs763888918 | snp | C/G | 1.6504e-05 | 0.00287258 | missense | FEM1C | GRCh38.p7 | 5:115525071 | TGCTGCATATCCAAA[C/G]CATACTTCCATAGGT | 56929 |
| rs764121190 | snp | C/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545671 | AAGCATAAAGGCTAC[C/G]AGGAATGGTAAACCC | 56929 |
| rs764135964 | in-del | -/AA | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520684 | CATGCAGTTGACAAC[-/AA]AAGTCTCCCCATATC | 56929 |
| rs764276443 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533706 | TCATGTCTTCTTTTC[A/G]CATTCTCAGAATGAG | 56929 |
| rs764284851 | snp | A/T | 1.65086e-05 | 0.00287298 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525487 | CACAATATTTGTGTG[A/T]CCAGTCACACTTGCT | 56929 |
| rs764353295 | snp | C/G | 1.65089e-05 | 0.00287301 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543387 | CCATTTGTTTTTTCA[C/G]AGATCAAGGAGGAAA | 56929 |
| rs764375708 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526867 | AACTGTATGTAGAAA[C/T]AATGCAGTTTATGCT | 56929 |
| rs764455988 | snp | A/G | 6.82722e-05 | 0.00584221 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524602 | GTCTCTGACGTTCAC[A/G]TCAGCACCACATTCT | 56929 |
| rs764475594 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527606 | CTCTACTATTCCCCA[C/T]GTTTTTCTAAGAAAT | 56929 |
| rs764545750 | snp | C/G | 1.80683e-05 | 0.00300563 | missense | FEM1C | GRCh38.p7 | 5:115524722 | AGGGCTGAAGTTATT[C/G]TTTCCCCTTGGATGC | 56929 |
| rs764670170 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537529 | GCACACCATCTACAG[A/C]TTAGTTTATCCAACT | 56929 |
| rs764766674 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539161 | CTGACTGATGAATGA[C/G]GACAGAATGTCTTCT | 56929 |
| rs764815308 | snp | C/T | 4.95258e-05 | 0.00497599 | missense | FEM1C | GRCh38.p7 | 5:115525053 | AAAGGATCCAAATTG[C/T]TCTGCTGCATATCCA | 56929 |
| rs764999142 | snp | A/G/T | 3.59004e-05 | 0.00423664 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524288 | TCGTGCTTTAACAGT[A/G/T]CTAAAATACAGTCAA | 56929 |
| rs765131954 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546708 | ACCAGCCTGGACAAC[A/G]TGGTGAAATCCCAAC | 56929 |
| rs765168856 | in-del | -/CACACACACACG | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546735 | AACTCCACACACACG[-/CACACACACACG]CACACACACATGCAC | 56929 |
| rs765255704 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532572 | GATCTTAAAGCAATT[A/C]TAACTTTTGTGTCAT | 56929 |
| rs765332480 | snp | C/T | 1.6495e-05 | 0.0028718 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525259 | TTCTGCACTGTTCAC[C/T]TCCTTGGCATAATCA | 56929 |
| rs765363662 | snp | G/T | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520562 | TTACAAATGAAAAGT[G/T]ATGGAAAACAAACGT | 56929 |
| rs765364944 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115543687 | CAGGGCACCAAACTA[C/G]AGAAAGAAAAAAAAA | 56929 |
| rs765430181 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527724 | GTAGCAAAAGCTGGC[C/T]AGGCGCGGTAGCTCA | 56929 |
| rs765485564 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542240 | AAACCGGAGCCCTTC[C/T]TCTGGACAAAGGTGT | 56929 |
| rs765602133 | snp | A/G | 1.65146e-05 | 0.0028735 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543252 | GGGGGAGCCCCCTCA[A/G]TGGTTTCGCCATCAA | 56929 |
| rs765696265 | snp | C/T | 3.29755e-05 | 0.00406038 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543356 | ATACCTGGCGGCCAT[C/T]AAGAGTGGCGTGGCC | 56929 |
| rs765723730 | snp | C/T | 1.65704e-05 | 0.00287836 | missense | FEM1C | GRCh38.p7 | 5:115524483 | CTAGCAGTTTGTTTG[C/T]GCAAGTTTGTGGCAT | 56929 |
| rs765838006 | in-del | -/T | 1.65079e-05 | 0.00287292 | frameshift-variant | FEM1C | GRCh38.p7 | 5:115525433 | TAGAGCATTAATACG[-/T]TCTGTCTTGCTGGTC | 56929 |
| rs765949546 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526514 | CTGACAACAGGCACT[G/T]GCACATTAGTAAAAG | 56929 |
| rs766004856 | snp | C/T | 1.80615e-05 | 0.00300506 | missense | FEM1C | GRCh38.p7 | 5:115524777 | TGCTTTTTGAAATGG[C/T]CTTGTTCTAGAGTAC | 56929 |
| rs766015701 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546830 | CACCTGAGCTGAGCT[A/G]GGGAGATCAAGGCTA | 56929 |
| rs766039249 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535016 | CTGTTTTACACCATA[G/T]AGAAATAAAATTGTA | 56929 |
| rs766049234 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533919 | TTCATTTGGAGAAAA[A/T]AAATATTCTGGCACT | 56929 |
| rs766075601 | snp | C/T | 3.31565e-05 | 0.0040715 | missense | FEM1C | GRCh38.p7 | 5:115524907 | GCTCTATTTCAAGGA[C/T]GCTTTTGCAAAGTAT | 56929 |
| rs766094540 | snp | A/G | 1.75465e-05 | 0.00296191 | intron-variant | FEM1C | GRCh38.p7 | 5:115525625 | AGTATTACCTTAAAG[A/G]GAGAGAGAAAAAAAG | 56929 |
| rs766094779 | in-del | -/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530486 | GAAGACCAAAACCAG[-/T]TAAGGATGAAGATTT | 56929 |
| rs766210034 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532724 | GTTTCTGTAACTACA[C/T]AGATTCTACATAATC | 56929 |
| rs766343685 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543161 | ATTGGTTAAAGTCGT[A/G]TTGTTGACAGATGCT | 56929 |
| rs766431531 | snp | A/G | 1.65638e-05 | 0.00287778 | missense | FEM1C | GRCh38.p7 | 5:115524474 | AGCAAGTCACTAGCA[A/G]TTTGTTTGTGCAAGT | 56929 |
| rs766454849 | snp | C/T | 1.6941e-05 | 0.00291036 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524311 | ACAGTCAAGTTATCA[C/T]CTATGAAGGGAAACA | 56929 |
| rs766495406 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531213 | CTCAATGAATAAATT[A/C]TATCTAATATAAAAC | 56929 |
| rs766635540 | in-del | -/TAAA | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522651 | GCATTGATGACTCCT[-/TAAA]TAGTGTAACATCAAC | 56929 |
| rs766696213 | in-del | -/TGTAGAGA | 1.7585e-05 | 0.00296517 | frameshift-variant | FEM1C | GRCh38.p7 | 5:115524636 | AGTATTGCAGTAACT[-/TGTAGAGA]TGGAAATTTACAAAC | 56929 |
| rs766753521 | in-del | -/CACACACACG | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546726 | GTGAAATCCCAACTC[-/CACACACACG]CACACACACATGCAC | 56929 |
| rs766823962 | snp | A/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522942 | CTGTGAGTGAGTGAG[A/T]GAGAGAGAGAGAGAG | 56929 |
| rs766866060 | snp | A/G | 1.64827e-05 | 0.00287073 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115542999 | TTCAAGTAAATACTG[A/G]GCAATCTCTTTATGT | 56929 |
| rs766944261 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527561 | ACTACTACACCAAGT[A/C]TATTTTAAACACTCT | 56929 |
| rs766988016 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539507 | TCAATTGCTATGACT[A/G]TTAAACTGAAGAGGT | 56929 |
| rs767099781 | in-del | -/TT | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522564 | AAGTCTAATGTTCTC[-/TT]GTTTATTTACTACTC | 56929 |
| rs767151134 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534224 | TCGTGCATTAAAGGG[A/T]GGTAGTATTCCTCAA | 56929 |
| rs767302186 | snp | C/G | 1.64963e-05 | 0.00287192 | missense | FEM1C | GRCh38.p7 | 5:115525240 | CAATAAGACCTTCTA[C/G]CTCTTCTGCACTGTT | 56929 |
| rs767386814 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542865 | TGTCAATGCTGGTTT[A/T]CTCAACACCAGTGCT | 56929 |
| rs767498039 | snp | A/G | 1.66319e-05 | 0.00288369 | synonymous-codon, missense | FEM1C | GRCh38.p7 | 5:115542966 | TTTGACACTTTTTCT[A/G]TTAACATCTGCCCCC | 56929 |
| rs767660533 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532322 | CTAAAGCTAAGGTAG[A/T]TTCTAAATTTTTAAT | 56929 |
| rs767670692 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546049 | TCCATAACGTTATGT[C/T]AGAAGTCATGCAGCA | 56929 |
| rs767691140 | snp | C/T | 1.85441e-05 | 0.00304495 | intron-variant | FEM1C | GRCh38.p7 | 5:115525644 | AGAGAAAAAAAGAAA[C/T]AACATACATTGAGGG | 56929 |
| rs767794210 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539751 | AATCAAGGACTGGCT[A/G]TCTTGTCTTATTGCT | 56929 |
| rs767878165 | snp | A/C | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522082 | ATTCTGCTGCAAAAC[A/C]GTGAGATGTGCCTCA | 56929 |
| rs768080272 | in-del | -/TTTG | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545941 | TGGACCTTCAATCAC[-/TTTG]TTTGAGGGAACTTAA | 56929 |
| rs768115858 | snp | C/T | 1.65015e-05 | 0.00287237 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525376 | TTTCAAAGCCCCAAG[C/T]AGATCTCTTTTTTTG | 56929 |
| rs768127246 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526773 | ACCTTTGGCTGGTAG[C/G]TGGGAACTTGGCTGG | 56929 |
| rs768276616 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542132 | TATCAAAATTATGCT[A/G]TCAAGGCAGTTGCTT | 56929 |
| rs768301943 | snp | A/G | 1.64925e-05 | 0.00287158 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543316 | TGCATTGCTCTAGGA[A/G]GAATTCCACCATGTC | 56929 |
| rs768342880 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538973 | TTCCTAGTCAGTACA[C/G]CCGCTCTAAAATCCT | 56929 |
| rs768344285 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528842 | ATGCTTAGCATATTC[A/G]AGGAGTTTTTTAAAA | 56929 |
| rs768388175 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523674 | AGTACTTTCAAAAAA[C/T]TAAGTTTGTAACAAA | 56929 |
| rs768430763 | in-del | -/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529009 | ATACAGAAAGAAGCA[-/G]GGAGTGGTAAAAGAA | 56929 |
| rs768641716 | snp | A/G | 8.3158e-05 | 0.00644764 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524560 | GTTGTTAAGAGCAGC[A/G]ATATGCAGGGGACTG | 56929 |
| rs768701493 | snp | A/C | 1.66263e-05 | 0.00288321 | missense | FEM1C | GRCh38.p7 | 5:115524865 | ACTGTAATGGGTCAG[A/C]TGGACACTGAGTTTG | 56929 |
| rs768760637 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534408 | CAAAAACATAGCTGT[A/G]TTTTGAGGAAGAACT | 56929 |
| rs768793278 | snp | C/T | 3.30562e-05 | 0.00406534 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525001 | AAAGGAGAATAGTTC[C/T]GCAAAAGATAATAAG | 56929 |
| rs768892127 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536977 | GGATGAGGACTAAAA[G/T]CAACTAATTATGTGT | 56929 |
| rs769130537 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545244 | GGGAGGCCTCACAAT[C/T]AAGCCAGAAGGGGAA | 56929 |
| rs769282944 | snp | G/T | 1.64982e-05 | 0.00287208 | missense | FEM1C | GRCh38.p7 | 5:115525221 | CTCATCTCATCAGGA[G/T]CAGCAATAAGACCTT | 56929 |
| rs769583032 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527204 | AGTTATATGGTGAGT[C/T]ACTTCCAAATTTGGG | 56929 |
| rs769705660 | snp | A/G | 0.00112631 | 0.0237042 | missense | FEM1C | GRCh38.p7 | 5:115524429 | TGATTTATAGGCTGG[A/G]TTAAATTTTTAGCTA | 56929 |
| rs769777618 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543116 | TATTTCCAAATGGCC[A/G]TCGAAACACGCAGCT | 56929 |
| rs769844540 | snp | A/G | 5.15548e-05 | 0.00507688 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543467 | GCCATCCCGAGCTGC[A/G]TTAAATACTGCTGTC | 56929 |
| rs769936124 | snp | A/G | 1.6964e-05 | 0.00291233 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524839 | CAAAATAATAGAAAG[A/G]GCCTTATTTAACTGT | 56929 |
| rs770029446 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523182 | GACCTTTGATATTAT[A/G]GCAGTAAATTGCATA | 56929 |
| rs770104121 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530911 | GTTACAAGAAAAAAC[A/T]GTAAATTAAATTAGA | 56929 |
| rs770164336 | snp | C/T | 1.64947e-05 | 0.00287177 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525334 | AGTCCTATCACTGTA[C/T]CTCATGTTCATTGCC | 56929 |
| rs770193731 | in-del | -/CAGT | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526669 | TACATAAAATTTCAA[-/CAGT]CAGTCATTTTAGGCA | 56929 |
| rs770201011 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545350 | TCAGCTCTCCTGAGA[C/T]GTACTCACTACCACC | 56929 |
| rs770263343 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531955 | TAAGTACTTCTCCCA[C/G]CACCAAGAACAAACA | 56929 |
| rs770317382 | snp | C/T | 8.23635e-05 | 0.00641677 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543086 | ATCAGCTTTGTGTTC[C/T]ACAAGGTACTTCACT | 56929 |
| rs770346486 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531537 | ATGATTCACTGTGCA[A/T]CTAACTCAGGGACTG | 56929 |
| rs770413502 | snp | A/G | 1.65381e-05 | 0.00287555 | missense | FEM1C | GRCh38.p7 | 5:115524411 | AGACACTGCAATGTG[A/G]TATGATTTATAGGCT | 56929 |
| rs770524546 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541919 | AATAGTGGTTGTCAG[C/T]GCATTAGAGATCTAG | 56929 |
| rs770682222 | snp | A/T | | | missense | FEM1C | GRCh38.p7 | 5:115542968 | TGACACTTTTTCTAT[A/T]AACATCTGCCCCCTT | 56929 |
| rs770686402 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527425 | CAAGATTTCAATGGT[C/G]TACAATGAAATAGTG | 56929 |
| rs770761053 | in-del | -/C | | | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544215 | CTCTCAGGAAATCCG[-/C]CCTGCCTTTTAGTCA | 56929 |
| rs770855189 | snp | A/G | 3.53832e-05 | 0.00420599 | intron-variant | FEM1C | GRCh38.p7 | 5:115542908 | TCAAACTTCCTGAAA[A/G]TAAGTGGTAGACATT | 56929 |
| rs770887791 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535571 | ACACACTTCCTAAAA[C/T]GGCTATATTAAAAAA | 56929 |
| rs770919300 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528618 | AAAGCCAGAAGCAAA[C/T]ATAAATACTATTTAG | 56929 |
| rs770935968 | snp | A/C | 1.65261e-05 | 0.0028745 | missense | FEM1C | GRCh38.p7 | 5:115525541 | ACCATCCTTTTCCAT[A/C]TTGGCACAATACATA | 56929 |
| rs770987634 | snp | A/C | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523471 | ACTGCATGATATATT[A/C]AGATGACAGACCTAA | 56929 |
| rs771012328 | snp | C/G | 5.02063e-05 | 0.00501005 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543446 | TTTGGTGAGAAGCCG[C/G]AGTTTGCCATCCCGA | 56929 |
| rs771051449 | snp | C/T | 3.29696e-05 | 0.00406001 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543342 | ATGTCAAGGTGCCCA[C/T]ACCTGGCGGCCATCA | 56929 |
| rs771071231 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540792 | GCTTTTAAAACATAT[A/C]CCAATTTGACTTAAA | 56929 |
| rs771139601 | snp | A/C | 1.67486e-05 | 0.00289379 | missense | FEM1C | GRCh38.p7 | 5:115524580 | GCAGGGGACTGTTGT[A/C]ATCCGAGTCTCTGAC | 56929 |
| rs771329351 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532081 | TAGAAATTTCAACTG[A/C]TTAAAGAGGTTTTCC | 56929 |
| rs771473009 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531000 | ATACAGCATTTTTTT[A/G]TATTCCCACATTTTA | 56929 |
| rs771491592 | snp | C/T | 1.64999e-05 | 0.00287222 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525193 | ACGTTCTCTGATTAA[C/T]AGTGCCTGCATTCTC | 56929 |
| rs771535142 | snp | C/T | 1.68775e-05 | 0.0029049 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525607 | TGCACAATCATGCAA[C/T]GCAGTATTACCTTAA | 56929 |
| rs771558231 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529007 | ATATACAGAAAGAAG[A/C]AGGGAGTGGTAAAAG | 56929 |
| rs771566494 | snp | A/C | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545117 | TCCCATCTCAGAGAC[A/C]CCAGAAGGGAAGTGT | 56929 |
| rs771619711 | snp | C/T | | | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543180 | TTGACAGATGCTCCA[C/T]GATTTAACAAGGACT | 56929 |
| rs771641302 | snp | C/T | 1.92391e-05 | 0.00310148 | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115524262 | TCATTTATGAAACAA[C/T]TGTTACCAATTCGTG | 56929 |
| rs771739705 | snp | A/G | 1.79648e-05 | 0.00299701 | missense | FEM1C | GRCh38.p7 | 5:115524667 | TACAAACAGGGTACC[A/G]CCCTACACATGTAGT | 56929 |
| rs771811063 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537271 | AACATATTTTATCAA[C/G]CAATCAATGAAAATC | 56929 |
| rs771972169 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538671 | TGAAAAACTTTTACT[A/G]GCATGAAAAATAAAA | 56929 |
| rs772047714 | in-del | -/GA | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522945 | TGAGTGAGTGAGTGA[-/GA]GAGAGAGAGAGAGAG | 56929 |
| rs772286001 | snp | A/T | 1.64738e-05 | 0.00286995 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543134 | GAAACACGCAGCTCG[A/T]AGAGGAGTTGAATTG | 56929 |
| rs772299303 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534700 | TAGATTCTGCCGTTT[A/G]TAAATTCCTCATGTA | 56929 |
| rs772367242 | snp | A/T | | | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524632 | TATCAGTATTGCAGT[A/T]ACTTGTAGAGATGGA | 56929 |
| rs772440586 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542056 | GCTTTTAAAAATTAG[A/G]TAGTGAATTATTTTG | 56929 |
| rs772818451 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539194 | AGCCAGTCTCCAAAT[A/C]TGAGCCTACAGCGTT | 56929 |
| rs772863992 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526308 | ACTTTCCCCAAAAAG[C/T]TCTCGTAAGAAAAAC | 56929 |
| rs772901223 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545343 | AAAACAATCAGCTCT[C/T]CTGAGACGTACTCAC | 56929 |
| rs772913411 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527247 | GATGCTCAACATAGC[A/G]TGTGTACCAGAAAGT | 56929 |
| rs772957782 | in-del | -/TAT | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536262 | CAATTAAAATAAAAA[-/TAT]TATATTTTTGGTGAA | 56929 |
| rs772966774 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533737 | AAAGACAATGAACAA[C/T]AAAACAACACAAAGT | 56929 |
| rs773064587 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540402 | TGTATGGGTATAAAG[C/T]TGAGGTTACGAGAAA | 56929 |
| rs773085413 | snp | A/G | 1.69735e-05 | 0.00291315 | missense | FEM1C | GRCh38.p7 | 5:115525611 | CAATCATGCAATGCA[A/G]TATTACCTTAAAGAG | 56929 |
| rs773244724 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534856 | CCAAGTGATACCTAC[A/G]CTGCTGGTCCTTGAG | 56929 |
| rs773257095 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115545378 | ACCAGAGCAGCATGG[A/G]GGAAACAGCCTTCTT | 56929 |
| rs773374439 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115521713 | GAGTGTAATTGGTTC[A/G]TTATTAAATTTACTC | 56929 |
| rs773394527 | snp | C/G | 3.31697e-05 | 0.00407231 | missense | FEM1C | GRCh38.p7 | 5:115524895 | GTTTGATAGCTCGCT[C/G]TATTTCAAGGACGCT | 56929 |
| rs773505437 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538361 | CTGTCTTACTTTGTT[A/C]CTTCAAGTCTTCATG | 56929 |
| rs773527909 | snp | A/C | 6.59522e-05 | 0.0057421 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543326 | TAGGAGGAATTCCAC[A/C]ATGTCAAGGTGCCCA | 56929 |
| rs773534468 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531033 | TAACTGTTGCCCCCT[C/T]TTAATCTTATATTAA | 56929 |
| rs773550467 | snp | A/G | | | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543901 | CAGGCAGTCTCCTCC[A/G]TGTGCGGAAAATTTA | 56929 |
| rs773610714 | snp | C/T | 4.96759e-05 | 0.00498352 | missense | FEM1C | GRCh38.p7 | 5:115524468 | TCATCCAGCAAGTCA[C/T]TAGCAGTTTGTTTGT | 56929 |
| rs773645686 | snp | C/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522099 | TGAGATGTGCCTCAC[C/T]ATAAGAGCATGTAAG | 56929 |
| rs773660894 | snp | C/T | 1.65162e-05 | 0.00287365 | missense | FEM1C | GRCh38.p7 | 5:115525030 | AGCTGCTGGCGGTCA[C/T]TGGGCTTAAAGGATC | 56929 |
| rs773710658 | snp | A/G | 8.2826e-05 | 0.00643476 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524929 | GCAAAGTATGCCCAT[A/G]AGATCATCAAATGTA | 56929 |
| rs773781743 | snp | A/T | 1.65007e-05 | 0.00287229 | missense | FEM1C | GRCh38.p7 | 5:115525379 | CAAAGCCCCAAGCAG[A/T]TCTCTTTTTTTGTCT | 56929 |
| rs773869893 | snp | C/T | 0.000116425 | 0.00762883 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525583 | CATGATGTCCAAACT[C/T]CCAGATTCTGCACAA | 56929 |
| rs773970244 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526605 | AACATTTTACTAATC[A/G]TCAAAATAGGAATTA | 56929 |
| rs774278781 | snp | A/G | 0.000865988 | 0.0207905 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524569 | AGCAGCGATATGCAG[A/G]GGACTGTTGTCATCC | 56929 |
| rs774284847 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537100 | GGAGGAAAAAAAGAA[A/G]GAAGACATGTTCTGA | 56929 |
| rs774521706 | snp | C/T | 1.8941e-05 | 0.00307736 | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543529 | GTGCTTTATTTATCT[C/T]TCAAAGCAGAGCTCC | 56929 |
| rs774601570 | snp | G/T | 1.80824e-05 | 0.0030068 | missense | FEM1C | GRCh38.p7 | 5:115524733 | TATTCTTTCCCCTTG[G/T]ATGCAGCTTAAGAAA | 56929 |
| rs774602449 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532134 | TCATTGTGAGAATGC[C/G]TGGTGAATAAATATA | 56929 |
| rs774771673 | snp | C/G | 1.74906e-05 | 0.0029572 | intron-variant | FEM1C | GRCh38.p7 | 5:115542932 | AGACATTTAGAAAAA[C/G]AAAGAAGCTGAACTC | 56929 |
| rs774775896 | snp | A/G | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546581 | ATGGGATTGTTAAGG[A/G]ATAGACGGACACTTA | 56929 |
| rs774805368 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533431 | TAAATGTAATTTTTT[A/G]TGAAAAAGTATAACA | 56929 |
| rs774889840 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115529237 | AAAAAGAAAAACACA[C/T]TGACATACAACACAG | 56929 |
| rs774949243 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540560 | CCCTCACATATAAGG[A/C]TAAAAGATGATAGTG | 56929 |
| rs775024503 | snp | C/T | | | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524368 | CCCTTTATAATATAT[C/T]CTATGATTCACTATG | 56929 |
| rs775053257 | snp | G/T | 1.64953e-05 | 0.00287182 | missense | FEM1C | GRCh38.p7 | 5:115525342 | CACTGTACCTCATGT[G/T]CATTGCCTTTTTCCA | 56929 |
| rs775097440 | snp | A/C/T | 3.30007e-05 | 0.00406195 | missense | FEM1C | GRCh38.p7 | 5:115525222 | TCATCTCATCAGGAT[A/C/T]AGCAATAAGACCTTC | 56929 |
| rs775230056 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537274 | ATATTTTATCAACCA[A/G]TCAATGAAAATCTGA | 56929 |
| rs775467577 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522090 | GCAAAACAGTGAGAT[A/G]TGCCTCACTATAAGA | 56929 |
| rs775467643 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538771 | CTACTTTCCAATTCC[C/T]GGACCCTCCAAGCAT | 56929 |
| rs775489971 | snp | C/T | 1.80673e-05 | 0.00300555 | missense | FEM1C | GRCh38.p7 | 5:115524712 | CCAGATGAAGAGGGC[C/T]GAAGTTATTCTTTCC | 56929 |
| rs775791314 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531679 | TTAAATTAATGGATA[C/T]GGCTGTTTCCCAACA | 56929 |
| rs775807693 | snp | A/G | | | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543225 | TGTCCTGCTGCAGAA[A/G]CGGCCCATAAAGGGG | 56929 |
| rs775945994 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543357 | TACCTGGCGGCCATC[A/G]AGAGTGGCGTGGCCC | 56929 |
| rs776011788 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527577 | TATTTTAAACACTCT[A/T]TTGTATTAAGGACCT | 56929 |
| rs776035759 | snp | C/T | 3.47319e-05 | 0.0041671 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543476 | AGCTGCGTTAAATAC[C/T]GCTGTCTTTAGATCC | 56929 |
| rs776128253 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542089 | GTCGTATAAATAGAT[C/T]CGTGTAAGGGAAGTT | 56929 |
| rs776191455 | snp | C/G/T | 6.61469e-05 | 0.00575064 | missense | FEM1C | GRCh38.p7 | 5:115524421 | ATGTGGTATGATTTA[C/G/T]AGGCTGGATTAAATT | 56929 |
| rs776217302 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537487 | GGACAAAGGACCACA[C/T]GGATATTTCCCTACT | 56929 |
| rs776274651 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538995 | TAAAATCCTATAGCA[G/T]GGATTGCTTATACTA | 56929 |
| rs776323442 | snp | A/G | 1.75984e-05 | 0.00296629 | intron-variant | FEM1C | GRCh38.p7 | 5:115542921 | AAATAAGTGGTAGAC[A/G]TTTAGAAAAACAAAG | 56929 |
| rs776323450 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540131 | GGGGAAAAATCCTCT[C/T]TTGCTGCTAAATCAC | 56929 |
| rs776356856 | in-del | -/TAA | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537658 | TTGGGATTAAAGTGT[-/TAA]TGACTTCAACTAGTA | 56929 |
| rs776438630 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523752 | AAAATATGCTAACAT[A/G]CAACAGTCAAGTTTA | 56929 |
| rs776490208 | snp | C/G | 1.65165e-05 | 0.00287367 | missense | FEM1C | GRCh38.p7 | 5:115525033 | TGCTGGCGGTCATTG[C/G]GCTTAAAGGATCCAA | 56929 |
| rs776638321 | snp | C/T | 0.000115391 | 0.00759487 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543344 | GTCAAGGTGCCCATA[C/T]CTGGCGGCCATCAAG | 56929 |
| rs776712528 | in-del | -/AAG | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535587 | GCTATATTAAAAAAG[-/AAG]AAGAAGAAGAAGAAC | 56929 |
| rs776726264 | snp | A/G | 1.68969e-05 | 0.00290657 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543455 | AAGCCGGAGTTTGCC[A/G]TCCCGAGCTGCGTTA | 56929 |
| rs776949203 | snp | G/T | 1.8011e-05 | 0.00300087 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524677 | GTACCGCCCTACACA[G/T]GTAGTATTCTTGTCC | 56929 |
| rs776951353 | snp | A/G | | | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543628 | AACGGATACACAACC[A/G]CGAAGAGTATGTTCC | 56929 |
| rs777057672 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530797 | GCCCAATGAAAATCA[C/G]AAAATTTTTTTAACT | 56929 |
| rs777071083 | snp | C/T | 1.64991e-05 | 0.00287215 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525196 | TTCTCTGATTAATAG[C/T]GCCTGCATTCTCATC | 56929 |
| rs777135740 | snp | G/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523358 | ACTTTGAAGTTAAAT[G/T]TAAGCAAATTCTCTA | 56929 |
| rs777192773 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543215 | CACCTTCAGATGTCC[C/T]GCTGCAGAAGCGGCC | 56929 |
| rs777449732 | snp | A/G | 1.66029e-05 | 0.00288117 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524371 | TTTATAATATATTCT[A/G]TGATTCACTATGACA | 56929 |
| rs777510410 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541578 | TTATTCTCACACAAG[C/T]GTGAAAAGACACATT | 56929 |
| rs777564760 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530375 | TTTCACCTAATAACA[C/T]AGAATTAAGTTACGT | 56929 |
| rs777628437 | snp | C/G | 1.6557e-05 | 0.00287719 | missense | FEM1C | GRCh38.p7 | 5:115524948 | TCATCAAATGTAACA[C/G]TAGTACCCAGCAGGC | 56929 |
| rs777816866 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528541 | CGCAAAAACTTAAAT[C/T]GAATTTAAGATCATC | 56929 |
| rs777860355 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115538560 | CTATGTAGTAGAATG[C/T]GGTTAGATGTCACAG | 56929 |
| rs778014759 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539878 | AATGCCAATAGCCTG[C/T]TAAAAAGTAATGAAA | 56929 |
| rs778104972 | snp | A/T | 1.65836e-05 | 0.0028795 | missense | FEM1C | GRCh38.p7 | 5:115524520 | GTGCACCTGATTTAA[A/T]AAGGAGATTCATGAT | 56929 |
| rs778167447 | snp | G/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546549 | CAGCCATCTTCAAAC[G/T]GAGCTCTGTATCCCT | 56929 |
| rs778283675 | snp | G/T | | | intron-variant, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115544028 | AGAGGCAGGAGACTC[G/T]GGTTCAGAAATGTTT | 56929 |
| rs778371792 | in-del | -/AG | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523905 | CAATAAAGTAGAAAC[-/AG]GGGGGAAACTTGAGA | 56929 |
| rs778476474 | snp | C/T | 4.94972e-05 | 0.00497455 | missense | FEM1C | GRCh38.p7 | 5:115525179 | GAAGGACCAAGAATA[C/T]GTTCTCTGATTAATA | 56929 |
| rs778496365 | snp | A/G | | | downstream-variant-500B | FEM1C | GRCh38.p7 | 5:115520891 | TCAAGTATTGAGTTA[A/G]TAAGAATACACTTAA | 56929 |
| rs778509931 | snp | A/G | 1.66532e-05 | 0.00288554 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543434 | GCTTGCCAACAATTT[A/G]GTGAGAAGCCGGAGT | 56929 |
| rs778572835 | snp | C/G/T | 2.31158e-05 | 0.00339961 | intron-variant | FEM1C | GRCh38.p7 | 5:115525669 | TGAGGGACCAAAATA[C/G/T]AATGTAATATATATA | 56929 |
| rs778645899 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115528636 | AAATACTATTTAGAG[G/T]AAGATATTATCATAT | 56929 |
| rs778680402 | snp | A/C | 3.29582e-05 | 0.00405931 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543005 | TAAATACTGAGCAAT[A/C]TCTTTATGTCCTTTG | 56929 |
| rs778847500 | snp | C/T | 1.65239e-05 | 0.00287431 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525013 | TTCTGCAAAAGATAA[C/T]AAGCTGCTGGCGGTC | 56929 |
| rs778878838 | snp | A/G | 1.77621e-05 | 0.00298006 | missense | FEM1C | GRCh38.p7 | 5:115524649 | CTTGTAGAGATGGAA[A/G]TTTACAAACAGGGTA | 56929 |
| rs778989836 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541141 | CATAAAACTCCATCA[A/G]TAGAAGAGTATGCAG | 56929 |
| rs779038214 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531574 | TTTTCCGGTAAAAGG[C/T]CAGGTAGCATTTTAG | 56929 |
| rs779143838 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115526984 | TTGAGCACTGGGTCT[A/G]TCATGGGTTTTCCTT | 56929 |
| rs779249877 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543044 | AATCATCAAGCACGT[A/G]TGCCCATGTCGGTTT | 56929 |
| rs779342361 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534769 | AAGCTGTGCTTCTCA[A/C]ACTTTCATGTATAAA | 56929 |
| rs779431394 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115540388 | TATCTATATGCATGT[A/G]TATGGGTATAAAGTT | 56929 |
| rs779473332 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536544 | AACTAACAGGTGTAG[A/G]TTGATGGAGGAGGTA | 56929 |
| rs779570095 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531821 | GCAGTACTGAAATGG[A/G]GTGGGCTGGATTTGA | 56929 |
| rs779623075 | snp | C/T | | | upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115546020 | GTAGGCAGTCTGACC[C/T]TCAGCATATGTAATC | 56929 |
| rs779710253 | snp | C/T | 1.76008e-05 | 0.0029665 | missense | FEM1C | GRCh38.p7 | 5:115524636 | AGTATTGCAGTAACT[C/T]GTAGAGATGGAAATT | 56929 |
| rs779988284 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544613 | TCCCCACCGCCGCCC[C/G]GGCCGCCCTGCTCCG | 56929 |
| rs780016776 | snp | C/T | 4.94907e-05 | 0.00497422 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543309 | GAGGCACTGCATTGC[C/T]CTAGGAGGAATTCCA | 56929 |
| rs780020074 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527880 | GTGGCACGCGCCTGT[A/G]GTCCCAGCTACTTGG | 56929 |
| rs780191349 | snp | A/C | 4.98608e-05 | 0.00499279 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115524557 | ATGGTTGTTAAGAGC[A/C]GCGATATGCAGGGGA | 56929 |
| rs780247083 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536508 | CAATAATGCTGATTC[C/T]AAGTATTTTATTCCC | 56929 |
| rs780305055 | snp | C/T | 1.65556e-05 | 0.00287707 | missense | FEM1C | GRCh38.p7 | 5:115524954 | AATGTAACAGTAGTA[C/T]CCAGCAGGCCTTTAG | 56929 |
| rs780358992 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534862 | GATACCTACGCTGCT[A/G]GTCCTTGAGTAGCAA | 56929 |
| rs780460207 | snp | A/T | 1.65408e-05 | 0.00287578 | missense | FEM1C | GRCh38.p7 | 5:115525552 | CCATCTTGGCACAAT[A/T]CATAAGAAGCATCTT | 56929 |
| rs780561900 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543278 | ATCAAAATTGACGGA[A/G]CCCCCAACTTCTATG | 56929 |
| rs780572054 | snp | C/G | 1.65899e-05 | 0.00288005 | missense | FEM1C | GRCh38.p7 | 5:115524538 | GGAGATTCATGATGT[C/G]TGGATGGTTGTTAAG | 56929 |
| rs780589757 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115536836 | ACAACAAAGTTAAAC[A/G]CTAAAAAATATCTGC | 56929 |
| rs780592221 | in-del | -/CCAG | 1.91459e-05 | 0.00309396 | utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543543 | TTTCAAAGCAGAGCT[-/CCAG]TTTAACTCTATCGAC | 56929 |
| rs780629576 | snp | A/C | | | intron-variant | FEM1C | GRCh38.p7 | 5:115534061 | CATTTCTCTAGAAAG[A/C]TAAAACAGTATGATA | 56929 |
| rs780693950 | snp | C/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115522989 | AAAGAAAGAGTGAGA[C/G]AAAGAAAGGAAGAAA | 56929 |
| rs780703564 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531842 | CTGGATTTGAACCCT[A/G]GGCCATAGTTTGCCA | 56929 |
| rs780850356 | snp | C/T | 1.74634e-05 | 0.0029549 | missense | FEM1C | GRCh38.p7 | 5:115524625 | CACATTCTATCAGTA[C/T]TGCAGTAACTTGTAG | 56929 |
| rs780988831 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115542758 | TAACAGAGTAACAGA[A/G]GTCTTTTATCACACT | 56929 |
| rs781047193 | snp | C/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523970 | ATTGTATAAAATTCA[C/G]AAACCAGTAAAGTAT | 56929 |
| rs781134954 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115527873 | GGGCATGGTGGCACG[C/T]GCCTGTAGTCCCAGC | 56929 |
| rs781239378 | snp | C/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541373 | ACAATGATCTTGTAT[C/G]ATTTTTATAAAAGAT | 56929 |
| rs781241182 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime | FEM1C | GRCh38.p7 | 5:115543088 | CAGCTTTGTGTTCTA[C/T]AAGGTACTTCACTAT | 56929 |
| rs781327148 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115537014 | CTCATCTAATGACAG[A/G]AAACTTCAACATTAT | 56929 |
| rs781495567 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115541150 | CCATCAGTAGAAGAG[C/T]ATGCAGCTATTGAAA | 56929 |
| rs781685553 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115531344 | CAAAATTCTACATCA[C/T]TGATTCTCAAAGCAC | 56929 |
| rs781708327 | snp | C/T | 1.64939e-05 | 0.0028717 | synonymous-codon | FEM1C | GRCh38.p7 | 5:115525304 | TGTCTGTGGCACTGG[C/T]TTACTAATAATATTA | 56929 |
| rs781708362 | snp | A/G | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523112 | ATCAAAGTAATTCAT[A/G]CAAGTTATCTTTAAA | 56929 |
| rs781774629 | snp | C/T | 1.65203e-05 | 0.002874 | missense | FEM1C | GRCh38.p7 | 5:115525528 | GAGTCATTCCATAAC[C/T]ATCCTTTTCCATCTT | 56929 |
| rs796195382 | snp | A/C | | | intron-variant, upstream-variant-2KB | FEM1C | GRCh38.p7 | 5:115544263 | ATTTCGATCACCCCC[A/C]ACCCCCCGCCAAGGG | 56929 |
| rs796196356 | snp | G/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115530293 | AAATACATAATTAGT[G/T]AAAAAAGGAAATATT | 56929 |
| rs796285234 | snp | A/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115533586 | TAACGATATATGCCA[A/T]GTACTATAGATTTAG | 56929 |
| rs796340730 | in-del | -/T | | | utr-variant-3-prime | FEM1C | GRCh38.p7 | 5:115523068 | CCTTTCATGTTTAAC[-/T]GGGGTGACAAATAAT | 56929 |
| rs796844016 | snp | C/T | | | intron-variant | FEM1C | GRCh38.p7 | 5:115535505 | TGAAAAAATGCTCAA[C/T]GTCATTAGCGATTGG | 56929 |
| rs796970203 | multinucleotide-polymorphism | AC/CA | | | intron-variant | FEM1C | GRCh38.p7 | 5:115539429 | CTCTGAGAAGGACTC[AC/CA]CTAATCACTACAGAT | 56929 |
| rs796983042 | snp | A/G | | | intron-variant | FEM1C | GRCh38.p7 | 5:115532844 | TTCAGAATTTTTACT[A/G]TTAAAATTAATGCTT | 56929 |