SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs76555174 | snp | C/T | 0.0169612 | 0.0905146 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72902561 | ATCACTGTCACAAGG[C/T]TGGAACTGGAAGGGC | 9873 |
rs76569812 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047554 | CACTGCCAAGGATAA[C/T]GCAAAAAGAAATCCT | 9873 |
rs76579313 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903610 | TCATTGCATTTACAT[A/G]CCTTGGGAAAGAGTG | 9873 |
rs76581108 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954155 | ATGCAAAGATAATAA[A/T]GGTGGCTTAGATTAT | 9873 |
rs76608021 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046005 | TTTTTTTTTTTTTTT[A/T]TTAGAGACAGGGTCT | 9873 |
rs76615529 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039194 | GTAAGCAATTCCTTT[A/C]GGATTCCTCATAAAC | 9873 |
rs76640911 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130273 | TTTCTTAGAGATAGG[A/G]TCTTGCTAAGTTGCC | 9873 |
rs76641528 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936751 | TGTATTTTTAACTCC[A/G]GAATTTATATTTGAT | 9873 |
rs76645433 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000744 | AATTATGCCGAAAAG[A/C]GGTATTACTAAAAAG | 9873 |
rs76654236 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966897 | CTGGGATGTGAACCC[C/T]GATTATGAGTTAAGA | 9873 |
rs76727972 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867701 | CTCTCTTTCACTTCC[C/T]GCAATAATTTTAAAT | 9873 |
rs76735116 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038349 | CCTGTCTCTTTAAGA[A/G]AAAAAAAAAAAAAGG | 9873 |
rs76749858 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028124 | ACTGCCTACTGGAGG[C/G]GTGAGAAGAGAGCCA | 9873 |
rs76757350 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101742 | GCACCCCCCGCCCCC[A/G]AAAAAAACACAACAC | 9873 |
rs76760498 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884456 | AGGTAATATAAATTT[A/G]GAAATAATGTGATTA | 9873 |
rs76762469 | snp | A/C | 0.0528381 | 0.153711 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838329 | CCCTCCTTCTGTTTC[A/C]TTATGTAGCCAACAT | 9873 |
rs76790176 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991535 | AGTGGGCTTCATCCC[C/T]GGGATGCAAGGCTGG | 9873 |
rs76793740 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882369 | TCTCAAAAAAAAAAA[A/G]GTACAGAGTAGAATG | 9873 |
rs76793820 | snp | A/G | 0.235564 | 0.249583 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908815 | ATGCCACTATGCCCC[A/G]CTATAGTTTTGTACT | 9873 |
rs76815220 | in-del | -/T | 0.0955749 | 0.196603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957020 | CAAAGGACTCTAGTC[-/T]TTTTTTTTTTTTCTT | 9873 |
rs76821975 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951893 | GTCCTTACTCCCATA[A/C]AACTTAGGGAAAATC | 9873 |
rs76849542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963929 | GTGTCATGAATAGAT[C/T]TCACAGTTGAATAAC | 9873 |
rs76871630 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143611 | TTTTTTTTTTTTTTT[G/T]GAGTCACGGGGCTGT | 9873 |
rs76873900 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006911 | TGAAACCAAATGTGT[C/G]TGGCTCCCAAACCTC | 9873 |
rs76904120 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020033 | TGATGCATAATGCTG[A/G]TTTGATTTGCAATTC | 9873 |
rs76916550 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870342 | GCTCCTTTAAGACTC[A/G]AGCATTGACATTCAG | 9873 |
rs76936742 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114876 | AAGCTACAAGCTGTG[C/T]GCCCAAAACTGAGGG | 9873 |
rs76941532 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869302 | AAGTTCTTCCTAATC[A/G]ATTAATTACAACAAT | 9873 |
rs76949292 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865367 | CTTTATTTATATTAT[C/T]AGATCTTCCACAAAA | 9873 |
rs76951135 | snp | G/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914979 | TTTTTTTTTTTTTTT[G/T]TTTTGCAAACTAAGC | 9873 |
rs76953154 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851217 | TTGAAAAAACAACCT[G/T]TTCACTGAAATTAAA | 9873 |
rs76967156 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108206 | TGTCAATGACTTCTT[C/T]TGAAAAATGTCCACT | 9873 |
rs76982282 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057335 | ACAGAAGCTAAAGAA[C/T]CACAAGGAAGAAAAA | 9873 |
rs77004023 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011061 | AGTGGCAGGGGTGGG[C/T]AGAACCAACCTCAGG | 9873 |
rs77006715 | snp | C/G | 0.030278 | 0.119257 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098148 | TAGGGTATAAAGCTA[C/G]GTTGTTAACTTGAAA | 9873 |
rs77038197 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091905 | AATTAGCTGGTAGCG[C/T]GCACCTGTAATCCCA | 9873 |
rs77041803 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936974 | TCCCTGTGTATGGGC[C/T]ATATATTCCTGTTTC | 9873 |
rs77066090 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999735 | TATTCTGATATTGAG[C/T]AAGGTGGCAGTAATT | 9873 |
rs77146803 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861931 | AGCGAAACGCCGTCT[A/C]AAAAAAAAAAAAAAA | 9873 |
rs77154202 | snp | G/T | 0.145642 | 0.227177 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103535 | TGTCTTATTGCTAAC[G/T]ATATTACATTGAATA | 9873 |
rs77175480 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871057 | AAAAGTTCCTATTCT[C/T]CAAATTCAAGAAAGG | 9873 |
rs77175727 | snp | G/T | 0.0126467 | 0.0785075 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73000992 | ATAAAAACAATACCC[G/T]TTTTAGTTGCTGTTC | 9873 |
rs77188826 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914309 | TGTGAGTCAGGTGCC[C/T]AGCCTGCCCTAAGCA | 9873 |
rs77193680 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023135 | TCTCCTTGACCTTTG[C/G]TGAAAAGTTTTAACA | 9873 |
rs77203641 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109729 | GCTAGGACTTCCAGT[A/G]ATACACTGAGTAACA | 9873 |
rs77204389 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966202 | TCTCACTCTGTCGCC[A/C]AGGAAGGAGTGCAGT | 9873 |
rs77217967 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127495 | AAAAGCCAAGAACAC[A/G]AGCCAGACTTACAAA | 9873 |
rs77230680 | snp | C/T | 0.0441612 | 0.141882 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897374 | ACATGTACAGACTTT[C/T]TTTCTTTGTCTTATT | 9873 |
rs77247067 | snp | G/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924652 | GGAAGTCTTCCATTG[G/T]ATCTTATGTTTGGCT | 9873 |
rs77254773 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044272 | TCAATTAAAAAAAAA[C/T]TTATGAATATTTCCA | 9873 |
rs77263609 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046174 | TTTTTAATGTTTTGT[A/G]AAGACAGGGGTCTTG | 9873 |
rs77310163 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880881 | TCGAAAAAAAAAAAA[A/G]GAAAACAACAACAAC | 9873 |
rs77315987 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095911 | GACTGGCTGAGGATT[A/T]AAAAAAAAAAAAGTT | 9873 |
rs77322995 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974937 | TTAGGTGAATCAGAG[G/T]TACAAGAGCTAGAGA | 9873 |
rs77340504 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896788 | AAAAAAAAAAAAAAA[A/G]AAGAAAGAAATATGC | 9873 |
rs77351594 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924085 | TTCACTTTCTTGAAA[A/G]TTTCTTTTGATGTAC | 9873 |
rs77360270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965437 | TTCTACCAGGTGAGA[A/C]AAAATAAGTCTTAAC | 9873 |
rs77363202 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134546 | TGGGAATCTACAGTT[C/G]AGAGAAAGTAACATA | 9873 |
rs77363286 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935887 | TTTTTCTATAAAGCT[C/T]GTGTTATCCTCTTGC | 9873 |
rs77393561 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038420 | TATAATTTATCCAGT[C/T]GAATCCTCTCAGATC | 9873 |
rs77393660 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066714 | GAAGACATTTATGTA[A/G]CCAACAGACATGAAA | 9873 |
rs77396132 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076249 | TTAGGCAGCATTATA[C/T]CTAATAACCAAATTT | 9873 |
rs77403018 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895643 | GAGAAAGGTGACTAA[A/T]CCAGTAGAGGGCCTA | 9873 |
rs77424910 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048183 | CCCAAAGCATTTGAG[G/T]CATAGCTAGAGCAGC | 9873 |
rs77429641 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136416 | AACACAAAAATTAGC[C/T]GCGCACCTGGAGTCT | 9873 |
rs77447505 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846026 | TAATATCTTCCTCAT[A/G]GGGTTATTGAAGGGA | 9873 |
rs77487804 | snp | G/T | 0.0648419 | 0.167978 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035150 | TTTTAGTTTTTATTT[G/T]TATGTATGTATGTAT | 9873 |
rs77502656 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934330 | CTATGAAGAGCCATG[C/T]CTTTTTTTTTTTTTT | 9873 |
rs77512961 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106405 | AATGAGACTCTGTCT[A/C]CAAAAAAAAAAAAAA | 9873 |
rs77557631 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898343 | CTATATCTTACGTAA[A/C]TTTAGATAAAATATT | 9873 |
rs77570823 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069520 | TCACTAACAAAGCAA[G/T]GGATAAGATAAAACC | 9873 |
rs77576882 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941978 | TATGATCAAATACTA[C/T]GCAGTCATTAAAATC | 9873 |
rs77605839 | snp | A/G | 0.00831782 | 0.0639509 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72868021 | TTCAGCTTTCAATTT[A/G]ATTATCTAGAGAACC | 9873 |
rs77639079 | snp | C/T | 0.226188 | 0.248863 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899361 | TTTTACCAAAGAAGA[C/T]ATATGAGTGGCTAAT | 9873 |
rs77656109 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858134 | GAGAATCCAGATAAA[G/T]AATCTGGTAATACCT | 9873 |
rs77663794 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840002 | AAACGAGGCAAATGT[A/G]GAGAAGCACATCAGC | 9873 |
rs77705768 | snp | A/C | 0.0123036 | 0.0774623 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838607 | AGAAAATGACAACAA[A/C]AAAAAAAGGCACGAA | 9873 |
rs77715619 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013200 | CCAGTTAACCTCTAA[A/C]CCACATACTTCACAG | 9873 |
rs77717172 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887460 | ATGCCACAATTAGCT[G/T]CCACCTTACCTCTGC | 9873 |
rs77718624 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075006 | GAGACTTTAACAGGC[A/T]CTTAATAACACAAAA | 9873 |
rs77731311 | snp | A/C | 0.0919752 | 0.193722 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967707 | GTGATGGTTGTACAA[A/C]CTAGTAAATATAATA | 9873 |
rs77754605 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097388 | TTTATTTATTTATTT[A/T]TTTTTTTTGCATCTC | 9873 |
rs77757462 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848339 | ACTCTCATCACACTC[C/T]GTCTCTATACCTGCT | 9873 |
rs77780279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063720 | CTCTTCTTGTTGAAT[C/T]GATCCCTTTACCAAT | 9873 |
rs77781108 | snp | A/G | 0.031825 | 0.122064 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125136 | ACCAGAAATGCTGAA[A/G]GAAGTTCCTTAAGCT | 9873 |
rs77786657 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980977 | TAATTCAGAAAAATA[C/G]ATATTTCCTTAACAT | 9873 |
rs77796017 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861936 | AACGCCGTCTCAAAA[A/C]AAAAAAAAAAAAAGA | 9873 |
rs77800942 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985571 | AAGACTCTAACAATA[C/G]GCTCTATGAAGTCCT | 9873 |
rs77809521 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111464 | TATCTTTCTCCATCC[C/T]TTTTTTTTTTTTCAG | 9873 |
rs77836591 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970656 | AAAGTCCATCCCTGT[A/G]AAATGCCACTGTCTG | 9873 |
rs77847109 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009052 | ATTTAAAAAAAAAAA[A/G]GGTCCAAGAGAAAGT | 9873 |
rs77853902 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130843 | GCATGTTACCTTTTA[C/T]TAATTATAAAATCAG | 9873 |
rs77884652 | snp | A/C | 0.138546 | 0.223781 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859704 | AAATCTGCAGAGGGT[A/C]CTCCTCAAGACTTTG | 9873 |
rs77894281 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966166 | CTTCTTTGAACTGAG[C/T]CTTTTTTTTTTTTCA | 9873 |
rs77907627 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859131 | AGCAGTCTCCCCTTA[C/T]GTGTGGTTTGGCTTT | 9873 |
rs77910635 | snp | C/T | 0.0119091 | 0.0762411 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837365 | CATGGGGACATTTGG[C/T]GAGCATTTCAAGTTT | 9873 |
rs77960535 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051176 | TAAAAATTAGCAGGA[A/C]GTGGTGTCACACATG | 9873 |
rs77963674 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010231 | TCAATGAATTCTTCC[A/C]TTACAGAATTTCTGT | 9873 |
rs77971648 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929435 | TTCTGGTGGGTAAGA[C/T]AGCTGGAGGCCTTCT | 9873 |
rs77981438 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060244 | TTTAAACAAATGTCT[A/G]ATTGTACCATATTTT | 9873 |
rs77983294 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084961 | AGAGTAAGAAGGAGG[A/G]AAAAAAAAAAAAAAG | 9873 |
rs77986964 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091400 | AAACAACAAAAAAAA[A/T]TAGCCAGGTGTGGTG | 9873 |
rs78005959 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119302 | AGCGAGACTCTGCCT[A/C]AAAAAAAAAAAAAAG | 9873 |
rs78059239 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040877 | TCCCTTCAACCTTCC[C/T]ACAAACTGCTCCCCC | 9873 |
rs78060984 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094384 | ATAATTAAACTTACA[C/T]TTATTTTGATATAAC | 9873 |
rs78061964 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923520 | TTAGTGATTAGGAAC[A/G]GTATATCTTTGTAGT | 9873 |
rs78063789 | snp | A/T | 0.0513262 | 0.151752 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876975 | TAATATGATCACTTC[A/T]TTTTTTTTTTTTTTA | 9873 |
rs78082263 | snp | C/G | 0.143959 | 0.226396 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875391 | TTTATTTGACAGAGT[C/G]TCGCTCTGCTGCCCA | 9873 |
rs78088433 | snp | G/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046006 | TTTTTTTTTTTTTTT[G/T]TAGAGACAGGGTCTC | 9873 |
rs78103413 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096424 | GATGTGGTGGCGGGC[A/G]CCTGTAATTCCAGCT | 9873 |
rs78104946 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885582 | TAGGGTACCAGTCGG[C/T]GATACCATGCATGGG | 9873 |
rs78106592 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936116 | GGGAAGACACTGACC[A/G]TTCTTGAGCTTTCCA | 9873 |
rs78113905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946953 | CCCTCTTTGTGGGAC[C/T]AGTCTTTGCAGCCAT | 9873 |
rs78115530 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882976 | ACAGACATATAGACC[A/G]ATGGAACTGAATAAA | 9873 |
rs78124059 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844906 | GAAAAATAATATTGA[A/G]GAAAAAACCCCACTC | 9873 |
rs78125524 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982043 | TATGGAAAATATATG[C/T]AGAGTTTTCATCTGA | 9873 |
rs78139650 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870321 | GCCTGTTTGATATAA[C/T]TGGGGGCTCCTTTAA | 9873 |
rs78165696 | snp | A/G | 0.0452528 | 0.143452 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143759 | ACTTCCCAGATGACC[A/G]CATGACCAGAAATTG | 9873 |
rs78167218 | snp | G/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850075 | TTTTTTTTTTTTTTT[G/T]TTTTTGAGATGGAAT | 9873 |
rs78186456 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060063 | TTAAAAGCAGGTAGG[A/G]TACACTGCTATCAGA | 9873 |
rs78195769 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996663 | AGAAAATCTTTAAAA[A/G]AACATGAACTTTAAA | 9873 |
rs78197229 | snp | A/C/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048276 | CTCATGCCATGTACC[A/C/G]ACACACATATGGGAC | 9873 |
rs78201152 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065150 | TGATTGTGGTGGATA[A/C]GCTTTTTGATGTGCT | 9873 |
rs78216886 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872352 | AATTCAGTGGCTTAC[A/G]GTATATTCATAGTAC | 9873 |
rs78217242 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998189 | TGGAATTATCTTGCT[A/G]GAAGATTTTTATATT | 9873 |
rs78218814 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030921 | TATCTCTATACTTGC[A/G]CGTCCTGAATTTCTG | 9873 |
rs78242798 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063672 | TCTTTTTTTGATCTT[C/T]GTTGGTTTAAGGTCT | 9873 |
rs78246085 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034501 | AATTCGGTACCAGAG[A/G]CTGAGCCTGTACCAA | 9873 |
rs78281067 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063799 | ATAAAGCAACTTCTT[A/G]GAGACCTACAAAGAG | 9873 |
rs78285898 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070750 | AATTAAAAAAAAAAA[A/G]GAAATTGAACAAGTT | 9873 |
rs78295328 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968092 | CAAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAGA | 9873 |
rs78329834 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127196 | ACACTTTTCATAACA[C/T]CAGAAATAACATTTT | 9873 |
rs78338303 | snp | A/G | 0.046775 | 0.145601 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084557 | CACCACATCTGGTTA[A/G]TTTTTAAATACTTCT | 9873 |
rs78339540 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109556 | ACTGATTTCTGTATG[C/T]TAATTTCATATCCTG | 9873 |
rs78345869 | snp | C/G | 0.0338708 | 0.126327 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982832 | TAAATTCAGGATAAA[C/G]GTAATGAAATTTTTT | 9873 |
rs78355612 | snp | G/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952341 | TATCTTTTTTTTTTT[G/T]TGAGACAGGGTCTCA | 9873 |
rs78373710 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949222 | GGGAGGCCCATGGCG[G/T]GCAGATCACCTGAGG | 9873 |
rs78392861 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084884 | GTTTAAAGACTTTAC[C/T]GTTATGTGCCAGGAA | 9873 |
rs78394787 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049686 | ACTTAGAGTATAATA[A/T]AAAAAAAAAAAAAAA | 9873 |
rs78400285 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051603 | CGACTTTATACTATT[G/T]TACACAAAAGTATGA | 9873 |
rs78420754 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086245 | AAAACTCCGTCTCTA[C/G]TAAAAATACAAAAAT | 9873 |
rs78484827 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017452 | CAACTACCTGCTTGA[A/G]GCAAAAATTACTCAA | 9873 |
rs78496443 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897691 | CCCATGTTTTCTCCA[C/T]TGTACACCACCTGTA | 9873 |
rs78519750 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953813 | GAGTGAGGGAGTATC[A/G]AGTTCTGTGGCTCTC | 9873 |
rs78560506 | snp | G/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009054 | TTAAAAAAAAAAAAG[G/T]TCCAAGAGAAAGTAG | 9873 |
rs78560848 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121657 | TAATTGTTAAGGGCC[A/C]AAAAAAAAAAAAGTC | 9873 |
rs78600286 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837467 | TTTCTTAACCAAGGA[A/G]AAAAAAAAAAAACAA | 9873 |
rs78601302 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048804 | CTCAAGAGAAAGGGT[C/G]GGGAATGAATATTTG | 9873 |
rs78632327 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084879 | CCTGAGTTTAAAGAC[C/T]TTACCGTTATGTGCC | 9873 |
rs78642949 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957760 | GAGGCATTATGTTCA[C/T]GATTTGCTCTCAAAT | 9873 |
rs78654834 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056378 | CTGCTAGGGAATACC[A/G]GTATTAGTAAAGAAC | 9873 |
rs78659915 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939027 | CAGGATATTTTCAAA[C/T]TTTAATACAGTAGCC | 9873 |
rs78680390 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047247 | CTACCATTTTTTTTT[A/T]AATTAAAGAAAAAGA | 9873 |
rs78691374 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912939 | GTTTAATTGACCCAT[C/G]GTTCTGCAGGCTGTA | 9873 |
rs78691864 | snp | A/C | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893749 | GGAGACTCTGTCTCC[A/C]AAAAAAAAAAAAACT | 9873 |
rs78693033 | snp | A/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924699 | TTTTTTTTTTTTTAA[A/T]TACACAAATTCTGTC | 9873 |
rs78715889 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968090 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 9873 |
rs78724679 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020594 | ACTTTAAAAGTAATA[C/T]AGAATTTCACTCCCA | 9873 |
rs78753085 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895031 | CACATATTTCAAATA[C/T]GCCACACACCTTGAA | 9873 |
rs78766352 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875499 | CCACCACATCTAATG[C/T]TAAAGTTTTTTGTAG | 9873 |
rs78782831 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054382 | CAGACAGGGGGCTAG[A/G]AAAAAAAAAGAAATT | 9873 |
rs78807111 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911552 | TTGAAAGAGACTGCA[C/T]TGAATCTGTAGACTG | 9873 |
rs78835923 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121662 | GTTAAGGGCCAAAAA[A/G]AAAAAAAGTCTACAT | 9873 |
rs78838741 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933234 | CTTAAATTAGGTCAT[A/C]CCTGGGATAGAGGCT | 9873 |
rs78849193 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855989 | GTTTCTTGCCCGCTA[C/T]ACCCAAGCACTTATT | 9873 |
rs78852731 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980696 | ATATATATATATATA[A/T]AATGTATGTATGTAT | 9873 |
rs78856007 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855905 | TACTCTTTGAACTAT[C/T]AGAATATGCACGTTT | 9873 |
rs78861246 | snp | C/G | 0.142609 | 0.225759 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978687 | GATGGTTTAAAAGTG[C/G]CACTTCCCCCTTCGC | 9873 |
rs78873590 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051849 | ATAATAGACCTTCAG[C/G]ATGCTAACACGGTAT | 9873 |
rs78888296 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875575 | CTCAAACGATCCTTC[C/T]GCCCTCCTGCCCTGG | 9873 |
rs78927304 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039530 | TCCAAAAAAAAAAAG[A/G]AAGAAAGAAAAGAAA | 9873 |
rs78982391 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876142 | GCAGCCTGGGCAAAA[C/T]AGCAAGACCCTATCT | 9873 |
rs78984730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980551 | TGGTTAGGATAATGC[C/T]AAGGCAATATTAAGC | 9873 |
rs79059902 | snp | C/G | 0.46875 | 0.121031 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065169 | CCACCACGATCAAGT[C/G]AGCTTCATCCCTGGG | 9873 |
rs79063774 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000237 | AAAATATTATTTCCC[A/G]AAATAATTACTTTAA | 9873 |
rs79069192 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850662 | CTGGCCAGGACAGAG[A/T]TTTTTTTTAAATCAA | 9873 |
rs79070889 | snp | G/T | 0.375 | 0.216506 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063777 | TTGCTTTATGAATCT[G/T]GGTGCTCCTGTATTG | 9873 |
rs79078438 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097296 | TGCAGGCGTGTAATC[C/T]CACTTGGTCGTGGTG | 9873 |
rs79094432 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921355 | ACTTTTAAATGAAAC[A/G]ACTGCTGTCAAAGAA | 9873 |
rs79117587 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871343 | AAACCCTATATATCA[A/G]CTCTTGCTTTGTTCA | 9873 |
rs79158392 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002046 | TGAAATTCTGATAGA[C/T]TATAATATTCATCTC | 9873 |
rs79181259 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938798 | AAACTATTGAAAAAA[A/T]TCTTATCAAGCTAAC | 9873 |
rs79183144 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002575 | AACTATTAATTTATA[C/T]TTAAAATACATTTTA | 9873 |
rs79185012 | snp | A/C | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033289 | CGAGATTCCGACTCA[A/C]AAAAAAAAAAAAAGT | 9873 |
rs79208044 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057803 | ACAGCTATACAGGGA[A/T]TGAGTTCCCCTCAGT | 9873 |
rs79214015 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912710 | TTGGTATTAGTTATT[C/T]TTTAAATGTTTGATA | 9873 |
rs79227805 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010314 | TGTTTTTCTGATTTC[C/T]CTGTACTGTTTTTCA | 9873 |
rs79256301 | snp | C/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022177 | TACTTTTAATGGTGA[C/G]TGAATGCTTTTCCCT | 9873 |
rs79257384 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124755 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAGG | 9873 |
rs79280809 | snp | A/T | 0.0520825 | 0.152737 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889479 | GAAAGTACAGAAAAA[A/T]CACATATAATGCTTG | 9873 |
rs79297540 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116929 | ATTATATTTTTTCAT[A/G]TAAAACCTTTCCATT | 9873 |
rs79305492 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848815 | CGTTCAAGTAAATAT[A/T]ATGGGAGGTGGTATC | 9873 |
rs79329636 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955102 | CCTGGAGAGCGTCAG[A/G]TCTCACAGACTGCTA | 9873 |
rs79336645 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961010 | GGGTAAATAGAAAAT[A/G]GTGACCTAGGAATGG | 9873 |
rs79339967 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077818 | CAGATGTGTTCATTA[C/T]CTTGCTTGTGATGCT | 9873 |
rs79351640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959671 | AATAAATTGCTAAGA[C/T]AGACATTTCAACGCA | 9873 |
rs79378475 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052014 | TTTCCAATGACACCA[C/T]AGTCTGATGAATTCA | 9873 |
rs79426191 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090913 | AGACCCATTAAGTAA[C/T]CACGCTTCATTCCCC | 9873 |
rs79429231 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080318 | AAAAAAAAAAAAAAA[A/G]AGAAAGAAAGAAAAG | 9873 |
rs79443180 | snp | A/C | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063775 | CCCAGTACAGGAGCA[A/C]CCAGATTCATAAAGC | 9873 |
rs79469405 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029493 | TCCCTGGCCCATTGG[C/T]AGGCAGCCATGCATA | 9873 |
rs79483878 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072619 | ACAGAAAATAATACT[C/T]AATTTTGCCCTGGTG | 9873 |
rs79504019 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887189 | CCATTAATCTCTGTG[A/G]TTTATTATGTACCTT | 9873 |
rs79569799 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013756 | AATTAGGGTTTATAA[A/G]CTAGCCTAGGAGCAT | 9873 |
rs79596649 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850663 | TGGCCAGGACAGAGA[A/T]TTTTTTTAAATCAAG | 9873 |
rs79611522 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977425 | GTAAAAAATATTTGT[A/T]AATTATCCAGTTGAC | 9873 |
rs79634977 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961634 | GTGACTTGAAGACAG[A/C]AATTCCCTACCCTGT | 9873 |
rs79638730 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913832 | AAAAACCCAAAAAAA[A/C]AACAAAAAAAAAAAC | 9873 |
rs79661690 | snp | G/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093619 | ATTTCTTTTTTTTTT[G/T]AGACCGAGTTTCGCT | 9873 |
rs79668918 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047951 | TAAGTAATTTATGTA[C/G]AGTGATTATGTTAAC | 9873 |
rs79685996 | snp | G/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093618 | GATTTCTTTTTTTTT[G/T]GAGACCGAGTTTCGC | 9873 |
rs79690010 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894305 | ATCCCAGTGTTCTGG[C/T]AGGCCAAGGCAGAAA | 9873 |
rs79725269 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913821 | AAAAAACCAAAAAAA[A/C]CCCAAAAAAAAAACA | 9873 |
rs79727431 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965711 | CTCTTTCCCATTCTA[C/T]GTACACCCCTCACCC | 9873 |
rs79745265 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918809 | GAAGGCATTTCCTTA[G/T]GGAGACAAAAAGCAA | 9873 |
rs79746021 | snp | C/T | 0.143959 | 0.226396 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070790 | ATGGTGACCTTAGAG[C/T]GTCACCATTCACTTA | 9873 |
rs79813422 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893750 | GAGACTCTGTCTCCA[A/C]AAAAAAAAAAAACTC | 9873 |
rs79836775 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080467 | TATGTATTTAACAAA[A/G]AAAAGACCAAGTTTA | 9873 |
rs79856396 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886825 | TCTCCCTATCTAGAG[C/T]AGGGAGTATTAGCCT | 9873 |
rs79892128 | snp | C/T | 0.039522 | 0.134904 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888769 | GGGAAGATAGGTGTG[C/T]GCCCCCATGCCCGAC | 9873 |
rs79906268 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122302 | CAAGTACAAAAACTT[C/G]CCCGTATTAGAGACT | 9873 |
rs79929666 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885385 | AGACTTAAATACTTG[C/T]ATTAGAAGAGGTGAG | 9873 |
rs79947899 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094743 | ATTATCAGCAAATTG[A/G]TAATTGTTTAATAAA | 9873 |
rs79959847 | snp | C/G/T | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106714 | GCTGTGTTTTTTCTA[C/G/T]GTTCAGAATCACAAA | 9873 |
rs79982450 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006495 | TGCTAGACTTAAAAA[A/T]TACCATGGAATTTAA | 9873 |
rs79999406 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861932 | GCGAAACGCCGTCTC[A/C]AAAAAAAAAAAAAAA | 9873 |
rs80012052 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858031 | TAGCATAAAGATTAA[A/C]TGAAGTAAAATATTT | 9873 |
rs80012643 | snp | G/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882370 | CTCAAAAAAAAAAAA[G/T]TACAGAGTAGAATGA | 9873 |
rs80015550 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088548 | TTCCTTTACTTTCTT[C/G]TTTTGCTTTCCATAA | 9873 |
rs80033263 | snp | A/T | 0.0715223 | 0.175059 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938944 | AAAAATATAGTAAGG[A/T]TAGGGTCACAGAAGT | 9873 |
rs80057058 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866271 | TTTTTGTTTTGTTTT[G/T]TTTTTTTTGTTTTTT | 9873 |
rs80096155 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986625 | GTGTTTGGGGATATT[C/T]CCAGTTCTCCTTTTT | 9873 |
rs80113739 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051750 | CAACAAAAAAAATTT[A/G]AAATAAATAGTAGTG | 9873 |
rs80114378 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040800 | ACTAATCCGACTGTG[C/T]TATAAAATACTAAAA | 9873 |
rs80115797 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003276 | AGAAATAACAAAAAT[A/G]CCTGCACCACTTACC | 9873 |
rs80119927 | snp | A/G | 0.144969 | 0.226867 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047759 | TCAAAATGCTATAAA[A/G]TGTATTGACTTTTTT | 9873 |
rs80126159 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125862 | CTATTATATAAAACA[A/C]TTCTTTTAGTAAAAC | 9873 |
rs80146192 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106407 | TGAGACTCTGTCTCC[A/C]AAAAAAAAAAAAAAA | 9873 |
rs80174420 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959974 | AAGCACAGATATATA[A/G]GAAGAAACCTACACA | 9873 |
rs80194265 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065133 | GGCAAACCAAATCTA[C/G]CAGCACACCAAAAAG | 9873 |
rs80196167 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880445 | CATCCCAGAAATAAT[A/G]TACTTATAGCCAACC | 9873 |
rs80212858 | snp | G/T | 0.0168055 | 0.0901129 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880611 | AAAATGATTAAAGAC[G/T]TTAAAAATAAACCCA | 9873 |
rs80213802 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918184 | ATTATTTTCTTAACC[C/T]TCTTTTTGGATCATT | 9873 |
rs80262507 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134775 | CTGATCGACAGCTCA[A/G]TGTATCAAAAAATAA | 9873 |
rs80285823 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006571 | CTCACCTTATGCCTA[C/G]ATTACTGCAACAGTC | 9873 |
rs80298780 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888682 | GGAGTTCAGAGGCAT[G/T]ATCTTACCTCAATGT | 9873 |
rs80316970 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981113 | CTGTACTGCAGACTA[C/T]AGAATTAGCATGAGG | 9873 |
rs80319951 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099808 | GGCTAGAAAGAGTGC[A/G]AAGGGAAGCCAGGAG | 9873 |
rs80333510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065308 | ACAAAATTAAACAGC[A/G]CTTCATGCTAAAAAC | 9873 |
rs80333555 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014607 | AAGAAATCATCTGAT[G/T]TCAATCATCACTGAC | 9873 |
rs80354696 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128867 | GTCAGGCTATAATTT[A/C]TTTTTATTTTTATTT | 9873 |
rs80356403 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003032 | AATGTATTAACTATG[-/A]AGACTGTACAATAAA | 9873 |
rs111265747 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111054 | GCTATTATTTCAGGG[G/T]TTTTTTTTAATGTTT | 9873 |
rs111271662 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901988 | CAAGTGATTCTCCTG[C/T]TTTAGCCTCCTGAGT | 9873 |
rs111288078 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72989004 | GTACTGCATGAGCCA[C/T]CTGTTCAGTCTCAAA | 9873 |
rs111307075 | snp | A/C | 0.0425829 | 0.139564 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141695 | CGGAAAGGCAACTCA[A/C]ACGCGCGCCCCCCAC | 9873 |
rs111320541 | snp | C/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084521 | TCAGCCTCCTAAGTA[C/G]CTGGGACTACAGGTG | 9873 |
rs111327773 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104600 | TTGAGACAGACTCTC[A/G]CTCTGTCACCCAGGC | 9873 |
rs111335495 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022368 | ATGTAAGAAACCCTG[A/C]AGAATCTACCAAAAA | 9873 |
rs111344181 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013904 | AGGCATGAGCCACCA[C/T]GCCCAGCCTAACTAT | 9873 |
rs111374724 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064166 | TACATGGAAATTGAA[C/T]AACCTGTTCCTAAAT | 9873 |
rs111376558 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928848 | TTTAGCATTAGGTAT[A/T]TCTCCTAATGCTATC | 9873 |
rs111377330 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956533 | AATCAACAGCATTAA[C/T]TTCTCTTACTTCTGG | 9873 |
rs111386020 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925217 | GAAAAGAAAATCAAA[A/G]TTCTGCTGGTACTTC | 9873 |
rs111390711 | in-del | -/A | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068505 | TATACTCCTGAAGTT[-/A]AAAAAAAAGTTGAGA | 9873 |
rs111394825 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72887551 | TGATACAGCAGCTCC[A/G]TGACACTCCAGATCA | 9873 |
rs111425392 | in-del | -/A | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032585 | TTACCTTCCTAACTG[-/A]AAAAAAAAAAAGCAC | 9873 |
rs111426684 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909964 | GCCCAGCTGCCCATT[A/G]TCTGGGAGGTGAGGA | 9873 |
rs111427631 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890138 | CATAAAACCATTAAA[A/G]ACCATAAGCTTTTTG | 9873 |
rs111437116 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948074 | GTGCAGTGGTGCGAT[C/T]TCGGCTCACTGCAAC | 9873 |
rs111482231 | in-del | -/AAAA | 0.0275645 | 0.114116 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054223 | TCTGGTCCTTTGCAG[-/AAAA]AAAAAAAAAAGTTTG | 9873 |
rs111484239 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958584 | ATGTAAACACCACGG[A/G]ACAAAATCTAATAAG | 9873 |
rs111490917 | snp | C/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134347 | TGGTGGTGCATGCCT[C/G]TGGTCCCAGCTACTC | 9873 |
rs111536891 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128903 | TTGAGACAGAGTCTC[A/G]CTCTGTTGCCCAGGC | 9873 |
rs111553274 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954764 | GAAAGCCAGATTTAT[A/C]AATGGTAAGGAAGAT | 9873 |
rs111573314 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928145 | GCTGGATAATGAGTA[C/T]GTGGGGGTCATTATA | 9873 |
rs111577880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969552 | CACAAAGTGGAACTT[C/T]AGGCAAAATTATCCT | 9873 |
rs111599136 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885472 | TCTAGTTTGGCATAC[G/T]ATGGAAATAATAGGT | 9873 |
rs111602928 | in-del | -/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087720 | AAAAAAAAAAAAAAA[-/T]TTTTTAAAATAAATT | 9873 |
rs111611038 | snp | G/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030944 | AATTTCTGCTATTTT[G/T]TATCCTTTGACCTAA | 9873 |
rs111615035 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987142 | TCTTCCTTCTATGGT[C/G]TCTCCTAATGTGTGC | 9873 |
rs111616537 | snp | A/C/T | 0.0291435 | 0.117316 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065888 | AATATTCCATGCTTA[A/C/T]GGCTAGGAAGAATCA | 9873 |
rs111676821 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039386 | AGCTGGGCATGGTGG[C/G]GCGTGCCTGTAGTCC | 9873 |
rs111678355 | in-del | -/A | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961177 | AGCTGCTCTACAAGT[-/A]TATCAAATCCAGGTG | 9873 |
rs111686502 | in-del | -/G | 0.342134 | 0.232404 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039249 | TCTGCAGGGTGCAGT[-/G]GCTCACACCTGTAAG | 9873 |
rs111710083 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119648 | GAGATGGGATTTCAC[C/T]GTGTTGCCCAGGTTG | 9873 |
rs111749204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119541 | ACAATTATAGCTCAC[C/T]ATAACCTCAACCTCC | 9873 |
rs111762225 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096370 | ACATGTTGAAACCCT[A/G]CCTCTACAAAAAAAA | 9873 |
rs111777107 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056837 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG | 9873 |
rs111785565 | snp | C/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887938 | AACATTACATAAGTG[C/G]AACACTGAATTTGAG | 9873 |
rs111796479 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104586 | TTACTTATTTATTTT[C/T]GAGACAGACTCTCGC | 9873 |
rs111804015 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134102 | ATAAATAAAGCCTTA[A/T]AAAAAAAAACTCTAG | 9873 |
rs111857648 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999076 | ACCATCATTTGAACC[C/T]CTAGATCCACCCATG | 9873 |
rs111873122 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946703 | ACAGAGTAATAGCTA[A/C]CATTTACAGAATATC | 9873 |
rs111883118 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841011 | GTTGTTGAGCAATAA[A/T]GCTGATGCAAGGCTG | 9873 |
rs111890322 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098697 | CTTCAACAAATGGTG[C/G]CAAGACAAGATTTCT | 9873 |
rs111918239 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043113 | GAGTGGTGAAAGTGG[A/G]CATCCTTGTCTTACT | 9873 |
rs111941738 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113494 | CCACCTCAGCCTCCT[A/G]AGTAGCTGGGACTAC | 9873 |
rs111948912 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836971 | CTTCCAAAAAATATT[C/T]TAAAATACAACAAAA | 9873 |
rs111960308 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129726 | TCATCCCAAAACCAT[A/C]CCCCTGACCCCACCC | 9873 |
rs111962346 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125346 | AATAACTGTAATTAG[A/C]CCATTGTAAGGTCGT | 9873 |
rs111970625 | in-del | -/A | 0.0287454 | 0.116389 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002598 | ACATTTTAAAATAAT[-/A]AAAAAAATGAAAAAG | 9873 |
rs111971075 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003784 | AAAATTTTATTTCAC[C/T]AGGTTTCATATGAAG | 9873 |
rs111981480 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983714 | ATTCTGCCTAGCTTC[A/T]ATAATTTATTGAAAC | 9873 |
rs111992518 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081941 | GGCGCGGTGACTCAC[A/G]CCTGTAATCCCAGCA | 9873 |
rs112011198 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965078 | ACAGGCATGAGCCAC[C/T]GCGCCTGGCCAATCA | 9873 |
rs112027563 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917953 | AAGGCCATTGGAATT[C/T]TGATAGGGACTACAT | 9873 |
rs112033048 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897910 | TTTACTTTTTCTAGA[A/G]AGAGCTCTGGCTTTC | 9873 |
rs112040956 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865008 | TAGCATGATACAGAA[A/G]GCAGAGTTAATACCC | 9873 |
rs112074658 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854463 | TAGAGACAGGGTCTC[A/G]CTCTGCTGCCCAAGC | 9873 |
rs112110292 | in-del | -/T | 0.365646 | 0.221644 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143596 | CCATGCCCAGGGAGG[-/T]TTTTTTTTTTTTTTT | 9873 |
rs112118937 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845458 | AAAAAAAAAAAAAAA[A/C]AAACAACAACAAACA | 9873 |
rs112120710 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051238 | GAAAATCAGTTGAAC[C/T]CAGGGGATTGAGGCT | 9873 |
rs112137719 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936108 | ATCACTCTGGGAAGA[C/T]ACTGACCGTTCTTGA | 9873 |
rs112187663 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853054 | TACTAGGCTTAGTAC[A/C]TGGGTAGTGAAACAA | 9873 |
rs112195448 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905804 | TAGTATTCCATGGTG[C/T]ATATGTGCTATATTT | 9873 |
rs112202410 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883935 | AGACCGTGTCTCAAA[A/G]AAAAAAAAAAAAAAT | 9873 |
rs112204807 | in-del | -/T | 0.0279526 | 0.114869 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057328 | AAGCAAAACAGAAGC[-/T]AAAGAATCACAAGGA | 9873 |
rs112218116 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992696 | GTGCTGGGAATACTG[C/G]CTAGCCATATGTAGA | 9873 |
rs112222854 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924239 | CACCACTGCATCTGG[C/T]TTACAAGTTTTAAAT | 9873 |
rs112237652 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077109 | TCTCAAAAAAAAAAA[A/T]AAAAGAAAAAGAAAA | 9873 |
rs112268354 | in-del | -/A | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038348 | CCCTGTCTCTTTAAG[-/A]AAAAAAAAAAAAAAG | 9873 |
rs112278425 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872156 | ATTTTTGGCTTAGAG[A/G]CACTCCAATTGGTAA | 9873 |
rs112283538 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079351 | ACAGGTACCCGCCAC[A/G]ACGCCTGGCTAATTT | 9873 |
rs112314567 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926491 | GCAGAGACAACTTGC[C/T]AGCAGAGAGGGGAGC | 9873 |
rs112325687 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890293 | CATGCCAACCTACTA[C/T]GGTGATAAAATCATT | 9873 |
rs112402361 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100930 | CTTCTGTCTGACAAC[A/C]CTTTTCTCAGAGCTC | 9873 |
rs112406958 | snp | A/G | 0.281313 | 0.248031 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093665 | GGAGTGCAATGACGC[A/G]GTCTTGGCTCACCAC | 9873 |
rs112420782 | snp | C/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998963 | TTAAGATTTATAAAT[C/G]TGGCACATTGGGGGT | 9873 |
rs112443096 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914099 | AGCTCGCTGCAAACT[A/G]CGCTTCCTGGGTTCA | 9873 |
rs112475514 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093772 | ATGCCGAGCTAATTT[C/T]TTTTGTATTTTTAGT | 9873 |
rs112512641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958128 | CACATGAAAACCTCA[A/G]CAATAAGTGTTCCCA | 9873 |
rs112513234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044554 | TGCACTCCAGCCTGG[A/G]TGACAGAGTGAGACC | 9873 |
rs112539842 | in-del | -/A | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134100 | TATAAATAAAGCCTT[-/A]AAAAAAAAAAACTCT | 9873 |
rs112576724 | in-del | -/T | 0.0509478 | 0.151255 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054682 | CTTTTCCTGTTATAA[-/T]TTTTTTTTTTCAGAC | 9873 |
rs112582480 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940700 | GGATTCATGTTCACC[A/G]TGGTGGCAGAAAACG | 9873 |
rs112603695 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931545 | GCCAAGGCAGGTGGA[G/T]CACAAGGTCAGGAGT | 9873 |
rs112614182 | snp | C/G | 0.097727 | 0.198275 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120153 | ATTATCTCCCACCAG[C/G]TCCCTCCCACAACAC | 9873 |
rs112614512 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082206 | GCTGGGCGTGATGGC[A/G]TGTGCCTGTCATCCC | 9873 |
rs112633302 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905600 | CCTAGCCCCCCACCC[C/G]CCGACAGGTCCCAGT | 9873 |
rs112656518 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098538 | ATTGGGTGGAGTGTT[A/C]TATATACACCTGTTG | 9873 |
rs112657585 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909566 | CTAGACGGGGTGGCA[C/G]CTGGGCAGAGGCGCT | 9873 |
rs112680047 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978920 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 9873 |
rs112681233 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021513 | GCTAAATGATGAGAA[C/T]ACATGAACACATAGA | 9873 |
rs112706814 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141494 | CTAAACAATCACACA[C/T]GCACAAGGCTCTGCA | 9873 |
rs112721728 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947871 | CAAATTCAAGACTAT[A/G]TTTTACATATTATTT | 9873 |
rs112722227 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934981 | TCCAGGTAGCTATTA[A/G]GCCACACACTCCCTT | 9873 |
rs112731104 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882691 | AATAAAAAATTAAGA[A/G]GCCAAAAAAGGAAAC | 9873 |
rs112742843 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028399 | GGGCCTGTAGCCCCA[C/T]TGTTTTGGCCAATTT | 9873 |
rs112744819 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847955 | CCTCATTTTCCCAAA[A/G]TGTTGGGATTACAGG | 9873 |
rs112748940 | snp | A/G | 0.0111196 | 0.0737302 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142160 | CGGAGACGGCGAGGG[A/G]GCGGGGGCCCCAGGA | 9873 |
rs112752699 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977304 | GTAATACCCTGTAAG[A/C]ACAGGCAATCAAAGC | 9873 |
rs112759795 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907033 | TGGCCATTTGTTTGC[A/G]TCCTCTTTTATTTCG | 9873 |
rs112763936 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865590 | TCCCTTCCTTCACAA[C/T]GAGAACAGCCCTTCT | 9873 |
rs112778193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952578 | GATCTACCGGCCTCG[A/G]CCTCTCAAAGTGCTG | 9873 |
rs112803780 | in-del | -/CA | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082316 | CACTCTAGCCTGGAT[-/CA]CAGAGTGAGACTTGT | 9873 |
rs112806939 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086269 | CAAAAATTAGCTGGG[C/T]GTGGTGGTGCGTGCC | 9873 |
rs112820916 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132718 | AGTCCTAGCTACTCC[A/G]GAGGCTGGGGTGAGA | 9873 |
rs112825943 | in-del | -/TTAA | 0.097727 | 0.198275 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033938 | AAACATTCAATAATG[-/TTAA]TTGTTTTAAAGAAAT | 9873 |
rs112858988 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921267 | TTTAATCTATCAAAT[C/T]TTGAAGAAAAGTCAT | 9873 |
rs112897475 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114839 | TCTCCTCTTCTCAAG[C/T]GGAAGGAGGGGGTCT | 9873 |
rs112943178 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088776 | AAAATGAACTAGTTC[A/C]CACTTTCACCATTTA | 9873 |
rs112953894 | snp | C/G/T | 0.0283406 | 0.115616 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985179 | TCACAATAAAATTAC[C/G/T]AAATATATTATTAAA | 9873 |
rs112954419 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908845 | TTTTTGTAGAGATGG[A/G]GTTTCACCATGTTGC | 9873 |
rs112962977 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014154 | TTTTTTTTTGGGAGA[C/G]AGAGTCTCACTCTGT | 9873 |
rs112980303 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004128 | AAAAAAAAAAAAAAA[A/T]AAAAAAAAGGATATC | 9873 |
rs113065770 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138880 | GCCAAAGTGCTGGGA[C/T]TACAGGTGTCAGTGA | 9873 |
rs113101952 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077104 | CTCTGTCTCAAAAAA[A/T]AAAAAAAAAGAAAAA | 9873 |
rs113102552 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133972 | ACATTTTAAATTGGC[A/G]TGACGATTGTACAAT | 9873 |
rs113107956 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870856 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTACAG | 9873 |
rs113155918 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886546 | GGCATTCTTTATGCC[C/T]TTCTAACAAGAACCT | 9873 |
rs113159872 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058797 | GGTCTTGAACTTCTG[A/G]CCTCAGGTGATCCGC | 9873 |
rs113160782 | in-del | -/AC | 0.0640965 | 0.167152 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121174 | TATACACATACACAT[-/AC]ACACACACACACACA | 9873 |
rs113169066 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966929 | AGTGGCCGGGCGCGG[C/T]GGCTCACGCCTGTAA | 9873 |
rs113180330 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859824 | AACTCACACAGGTCT[C/G]AGAATAACTCCTGCT | 9873 |
rs113188552 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843738 | ACCATAACAAAAACT[C/G]AAGAAACTGAATCCT | 9873 |
rs113189295 | snp | A/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071269 | CGTGCATACACATGA[A/T]ATCTATAATGGAGGC | 9873 |
rs113195592 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118054 | AGGCCCAGTGGCTCA[A/C]ACCTGTAATCCCAGC | 9873 |
rs113196005 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056822 | GCGCGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 9873 |
rs113199051 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995764 | TGAGTATGACAGAGA[C/T]ACAATAATAAACTTG | 9873 |
rs113207050 | snp | G/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907599 | GAGATAATCACGTGG[G/T]TTTTTTTTTTTTTTT | 9873 |
rs113219882 | snp | C/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887906 | TATGGCATTAAGTTT[C/G]AGGTGGTTTGTTAAG | 9873 |
rs113229757 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853234 | AGGATGCCAAGACCA[C/T]TCAGTGGAGGAAAGG | 9873 |
rs113245631 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074319 | ATATCATAGAATAAA[A/G]CTCTGTATGTGCAAG | 9873 |
rs113246963 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133736 | AGGCGGAGGTTACAA[C/T]GAGCCGGCATCGCGC | 9873 |
rs113249286 | in-del | -/A | 0.0456336 | 0.143994 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878952 | CTCTACTAAAAATAC[-/A]AAAAAAAATTAGCTG | 9873 |
rs113274192 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896291 | GTGTATTCTCATTCC[A/G]ACTGGGAAACCTGAG | 9873 |
rs113275345 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971596 | GAGCACCTCTAGGAG[C/G]TGAGAATGACCCCAG | 9873 |
rs113285427 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883772 | CCCATCTCTACAAAA[A/C]AATAGAAAAATTAGC | 9873 |
rs113290402 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878570 | ACTAGGAAGAAAGTA[C/T]TCAAGGACTAACGGG | 9873 |
rs113292837 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940503 | GTAAGCCAAGATGGG[G/T]GCATACCCGCACATC | 9873 |
rs113309736 | in-del | -/A | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016303 | GTGAGGCTCTGTCTC[-/A]AAAAAAAAAAAAAAC | 9873 |
rs113313804 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105023 | ATAATCCCTGCTAGT[A/G]AAGTACTTCAAGTTT | 9873 |
rs113326682 | snp | A/G | 0.279991 | 0.248195 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986271 | TCGGAGTGCAGTGGC[A/G]TGATCTCTGCTCACT | 9873 |
rs113340414 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958292 | GAAGGCTGAGGCAGG[C/T]GGATCACTTGAGGTC | 9873 |
rs113340921 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890114 | AAGTTACCAGAAGAG[A/T]AAGATCAGCATAAAA | 9873 |
rs113346682 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099307 | AGAAAATAATAAGCA[C/T]TGGCCAGGATGTGAA | 9873 |
rs113355644 | snp | A/G | 0.225005 | 0.248747 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874348 | CATGCCACCATGCCT[A/G]GCTAATTTTTTAAAA | 9873 |
rs113357204 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905093 | TGTCCTAATTCCCAA[A/C]ACCTGTGAATGTTAC | 9873 |
rs113361290 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044898 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 9873 |
rs113414727 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992594 | AACAGAGCCCTCAGA[A/G]ATAATGCCACATATC | 9873 |
rs113420418 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012079 | ATACTTATGTTCATA[C/T]AGAACTTATTCACTG | 9873 |
rs113422490 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928992 | GTTTTTTGTCCTTGC[A/G/T]ATAGTTTGCTGAGAA | 9873 |
rs113426864 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977186 | CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 9873 |
rs113432199 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058770 | ATGGGGTTTTACCAT[A/G]TTGGCCAGGCTGGTC | 9873 |
rs113436162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916037 | CACATGGGAACAACG[C/T]ACACTAGGGCCTACC | 9873 |
rs113447165 | in-del | -/A | 0.5 | 0 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838605 | ATAGAAAATGACAAC[-/A]AAAAAAAAAGGCACG | 9873 |
rs113474461 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953357 | TTTCAAAAAATCTTT[A/C]ATCTCTAATTCTGCT | 9873 |
rs113495402 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081930 | ATTCAAGATCGGGCG[C/T]GGTGACTCACGCCTG | 9873 |
rs113501899 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076107 | GCCTGGGCAACAGAG[G/T]GAGAACCCATCTCAA | 9873 |
rs113511914 | in-del | -/AGTT | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050994 | AAGCAATTTGACATC[-/AGTT]AGTTTGTTATCTATA | 9873 |
rs113549727 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080296 | AGCAAGACCCTGTCT[C/T]AAAAAAAAAAAAAAA | 9873 |
rs113560473 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063765 | TATACATGCACCCAA[C/T]ACAGGAGCATCCAGA | 9873 |
rs113561444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999445 | CTGTCTCAGCCTCCC[A/G]AGTAGCTGGAACTAC | 9873 |
rs113569546 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989566 | TCTGAGTAGTCTGAC[C/T]TGGTAAGTCCAAGGT | 9873 |
rs113583431 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862919 | CAAGAAACAGACCCA[C/T]ACATATATGATTAAT | 9873 |
rs113593662 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003738 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 9873 |
rs113605367 | in-del | -/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916242 | AAAAAGGTTTATCAA[-/T]TTTTGTTAATCTTTT | 9873 |
rs113620730 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950571 | TTGTGCCAGTACAAT[C/T]TGTTGAAAGACTATT | 9873 |
rs113631395 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131009 | ATACTAATTGAGAAG[C/T]AACTATGATTGTTGA | 9873 |
rs113645062 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957031 | AGTCTTTTTTTTTTT[C/T]TCTTCTTTTTTTTTA | 9873 |
rs113655714 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986399 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 9873 |
rs113666130 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118571 | TTCACCCACATTGAT[A/G]TGTGTATCCATAATT | 9873 |
rs113673316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900655 | AATGTGAATAAGTCA[C/T]TGGCAAAAGCTGATT | 9873 |
rs113674515 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867625 | TGGTAGATAGGCATC[A/G]ATAACCCAAATAGTG | 9873 |
rs113694306 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917141 | AGGCACCCACCACCA[C/T]GCCCAGCCAATTTTT | 9873 |
rs113701028 | in-del | -/AA | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050845 | TAAGAAAAATAATAT[-/AA]GACTCAGAACACCCC | 9873 |
rs113704626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085835 | GTTACCACATTATTA[C/T]ATTCAAATCTCCAGT | 9873 |
rs113725147 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000813 | ACATTCATTTTTAGC[A/G]GTTAATAAAACATAG | 9873 |
rs113725323 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070572 | GGTATTACAGGCGCC[C/T]GCCACCATGTCTGGC | 9873 |
rs113726693 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954082 | CTATTACGCAGAGAA[C/T]AGACATAAAGGTAGG | 9873 |
rs113741656 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912903 | AACTACCTGAGACTG[A/G]GTAATTTATAAAGAA | 9873 |
rs113745103 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854398 | AATGTGGTATACATA[C/T]ATACGATGGAATATT | 9873 |
rs113786055 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134138 | ATTAGATTACCTCTA[A/G]GATCTCTTTCTAGAT | 9873 |
rs113807150 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073083 | AGCATTCTGCCAAAG[A/C]CTACAGGAAGTACTT | 9873 |
rs113807821 | snp | C/T | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015523 | ATTTGTGTTCCATTG[C/T]CACCTGCCTTCTTTA | 9873 |
rs113811560 | in-del | -/C | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021385 | TGCAGCCATAAAAAA[-/C]AATGAGATCATGTCC | 9873 |
rs113813070 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894650 | GTAAAAAGCATCTGG[A/G]TCTCTGTATTCCAAC | 9873 |
rs113820890 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091912 | TGGTAGCGTGCACCT[A/G]TAATCCCAGCTACTC | 9873 |
rs113840704 | in-del | -/A | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852662 | GAGCAAGATTGTCTT[-/A]AAAAAAAAAAAGACA | 9873 |
rs113841029 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098837 | CAGGGGCAATTCTTC[A/G]TGACCTTGGATTTTG | 9873 |
rs113852908 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044447 | TAGATGGGCATGGTG[A/G]CACACACCTATAGTC | 9873 |
rs113873443 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095150 | TCTTATTTCTTATTA[A/C]TTAGGTGACCTTGAG | 9873 |
rs113876218 | snp | A/C | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030575 | CTCTTACCTGATGAC[A/C]TTAACTTTGTAAAGA | 9873 |
rs113877361 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087574 | GCCAGGCATGGTGGC[A/G]TGTGCCTGTAGTCCC | 9873 |
rs113958825 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982286 | AAGGAAAGAACTTGC[A/C]GTTTCTGGCCAGAGT | 9873 |
rs113972769 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026757 | CCTGCTAGGAGGTGA[C/T]TGGATCACAGGGGCA | 9873 |
rs113974510 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081583 | CCAGGCTGGAGTCCA[A/G]TGGCACTATCTGAGC | 9873 |
rs113990312 | in-del | -/A | 0.5 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094877 | AAATATTTTTTAACG[-/A]GGCAAGCGGAACGAA | 9873 |
rs114000235 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854809 | GGAGTTATTGCTTAA[C/T]GGCCAGAAAGTTTTA | 9873 |
rs114002424 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840592 | TTTCACAATTAGCCC[A/G]CTTTAATGCTCATAA | 9873 |
rs114008928 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080993 | AATAAAATAAAGAAA[C/T]AGAAATAATCACCAG | 9873 |
rs114049775 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050582 | GAACCCAGGCCCCCA[C/T]AATGGTTTTTCAGTA | 9873 |
rs114054917 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921309 | TCTCTGCATACAATG[G/T]GACATGTCAGCAAAC | 9873 |
rs114173737 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964111 | ATATAGTTAATATTA[C/T]GGATGACACAATCAG | 9873 |
rs114176709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857140 | TCCCATGGAAGGCAG[A/T]AAGAAGGCTGCAGTG | 9873 |
rs114215734 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132314 | AATACCTACCATTCT[G/T]GGCATTTCACCTGTC | 9873 |
rs114220643 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995425 | CCAAAAACTGGGCCA[A/G]GTGCGGTGGCTCACA | 9873 |
rs114237301 | snp | A/G | 0.030665 | 0.119967 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890655 | GTGCAAGGTACTATG[A/G]AAAGTGCTTCATATA | 9873 |
rs114243110 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935879 | CAATGCTGTTTTTCT[A/G]TAAAGCTTGTGTTAT | 9873 |
rs114257207 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023735 | CTTCTGGCAGCTTTA[C/T]TGATAAACTTGGCAA | 9873 |
rs114258122 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143250 | GCCTTTCTAAAGGTT[A/G]CACAGCAGGACTAGA | 9873 |
rs114259149 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074979 | ATAAATCAATAAGAG[A/T]AAAGCCAACAAGAGA | 9873 |
rs114266847 | snp | G/T | 0.030665 | 0.119967 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877055 | CGGCTCAGTGCAGCC[G/T]CAACCTCCAGGCTGC | 9873 |
rs114296380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133289 | ATCCAAAAGAAAAAC[A/T]TATATCCATACAAAA | 9873 |
rs114301773 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916072 | GGTAGAGGGTGGAGG[G/T]TGGGAGGAGGGAGAG | 9873 |
rs114327330 | snp | A/G | 0.021333 | 0.101051 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072066 | AAACAACAAATGAGT[A/G]AAGACATACGCAGAC | 9873 |
rs114328398 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056416 | ATACCCCCAAAATGT[A/T]ATCTTTTTAAAAATT | 9873 |
rs114333094 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060987 | AGAACTGTTGATAAA[C/T]AGAAGCAAAAGAAAA | 9873 |
rs114340239 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886160 | CTTGTATTGGGTCCC[C/T]GAAAGATGCTTGCCC | 9873 |
rs114409985 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099603 | ATATACATACAACCG[A/G]GTATTATCCAGTCAC | 9873 |
rs114415082 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109986 | TGATACGATGTATCA[C/T]ACTGACTGATTTGCA | 9873 |
rs114420234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918430 | CAATGGTTAATAGCG[A/G]TGGTGAAAATGGGTA | 9873 |
rs114435156 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007856 | TGTACTACAGTTATG[C/T]AAGATATTACCACTG | 9873 |
rs114457721 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042212 | CTACAGGCATGCGCC[A/T]CTGCACCCGGCTGAG | 9873 |
rs114465769 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942167 | CACAGTAATGAGAGC[A/G]TTCTCACTCTATAAG | 9873 |
rs114472634 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112263 | TTTTCACCAGACATA[C/T]CACTCTAGGGTAAAA | 9873 |
rs114495105 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941030 | GGCTTGGAAAGGACC[G/T]TATGTTCCACCATGC | 9873 |
rs114499039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017045 | TGGAGTGCAGTGGCG[C/T]GATCATGGCTCAATG | 9873 |
rs114500143 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058201 | TATTCTTTAAAGGTA[C/T]TGGACCATTATTGTT | 9873 |
rs114582333 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923887 | GAGGTTGCAGTAAGC[C/T]GAGTTTGTGCTATTG | 9873 |
rs114626975 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041882 | ATGTCAGTAGTTTTA[C/T]AGTTTTGGGTCCTAG | 9873 |
rs114634336 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951875 | TTCAGTATAGCAGAG[A/G]AAGTCCTTACTCCCA | 9873 |
rs114667785 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999615 | GTGAGCCACCACACC[C/T]GGCCTTATCAAACAT | 9873 |
rs114668595 | snp | C/T | 0.029116 | 0.117091 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092431 | AGGCACAAGCCACCA[C/T]ACCTGGCCCGGCATC | 9873 |
rs114673292 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055008 | GGACTGTGGTTCCAC[A/G/T]TGGCTGGGGAGGCCT | 9873 |
rs114675965 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995780 | ACAATAATAAACTTG[C/T]TAATAACTTGAATAT | 9873 |
rs114690823 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051133 | CTAGTCTGGGCTAAC[A/G]AAGTGAGACCCTGTC | 9873 |
rs114705375 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994376 | CCTTGAAACGACTCT[A/T]TGAAAAAGGTAGTAG | 9873 |
rs114706437 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110496 | TGTTCATAGTACCCA[G/T]GAATAATCTTTTTAA | 9873 |
rs114735374 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024575 | CATGGGGGTAAATTA[C/G]AGTCACAGACATCAA | 9873 |
rs114739106 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926432 | ATAGCTGGAGACGAT[A/G]GGATGGCCAGCTGCA | 9873 |
rs114741122 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851045 | TGGAGACTAAGTGAG[A/C]CAAGAAAGATTGCAC | 9873 |
rs114764285 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106377 | CACCACTACACTCCA[C/T]CCTGGGTGACAGAAT | 9873 |
rs114764446 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093238 | CTCTCTTAGACCCTG[C/T]CCTGTACACCTCTTC | 9873 |
rs114766548 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138061 | TAGGATACTAGTATA[C/T]TGCAAGCAAAATGTG | 9873 |
rs114766719 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046035 | TCATTTTGTCACCTA[A/G]GCTGAAGTGCAGTGG | 9873 |
rs114769135 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873950 | AAAAAAGGATACTAC[C/T]GTGCCACTTTAACCA | 9873 |
rs114772218 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937424 | AAATATAAAGCCTTA[G/T]TGTTAATTCAGTAAA | 9873 |
rs114773324 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101202 | CATTTATTCATAAAA[A/G]GGCCACATAAAATAG | 9873 |
rs114844612 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078406 | ACCTTTGTTTAGAAG[A/C]CCTAGTCAAAAGTCA | 9873 |
rs114849157 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867575 | TCTATTACTTCCAGA[A/C]ACGAAGCATATTTAC | 9873 |
rs114865273 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931914 | AATGCCATTGTTTCA[C/T]TGTTGTTGTTTTAAA | 9873 |
rs114865497 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995472 | TTTGGGAGGCTGAGG[C/T]GGCCAGATATCTTGA | 9873 |
rs114875020 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949117 | CAAAGTTGTGCAACC[A/G]TCACCATTACCTAAT | 9873 |
rs114876231 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839837 | ATGGTTATCATAGCT[A/G]TGGAAGTAGATGAGG | 9873 |
rs114895480 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852741 | GAAGACATGAAATCA[A/G]CCTAAATACTAATCA | 9873 |
rs114905990 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024043 | AAGGGTGGTGAACTA[A/T]TATACATAGTATTGT | 9873 |
rs114942058 | snp | A/G | 0.00426843 | 0.0459999 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841540 | GGCTGGTCGTACAAC[A/G]GCAGTGGAGGCAGGG | 9873 |
rs114983577 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916714 | GATATGTGATGTGCA[A/G]ATATTTTCTCTCATC | 9873 |
rs115011804 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987560 | TGGCATTCCTTACTC[C/T]ATAGTTGAAAAGTTA | 9873 |
rs115044150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857094 | CTAAACATTCCTTTT[C/T]TCCTCCTTTATTTGG | 9873 |
rs115044314 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929494 | TAGAGTTAATGCAGG[A/G]GATACAAAAATTAAG | 9873 |
rs115089126 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008454 | TTGTTATTGGTAGTA[A/G]AAAGGGAGAATATCC | 9873 |
rs115091392 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049955 | TTTGCTCAAGATAAA[C/T]AGAAACTAACTATAA | 9873 |
rs115124293 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965520 | TCTAATTACATTTGT[A/C]CATACTGCCATTATA | 9873 |
rs115125910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114919 | AGTACTCCCTCGGAC[A/G]CCATGGCTGGTGTCT | 9873 |
rs115153113 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059079 | TCAATTCAACAAACA[C/T]GGATATAAATGTAAA | 9873 |
rs115160909 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927813 | TCCTGAATAGGGTCA[A/G]GAGCACCAATAGGTA | 9873 |
rs115167696 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919468 | CTAAAGAGAATATAG[C/T]AGAAGATCATGGAAA | 9873 |
rs115181409 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987565 | TTCCTTACTCTATAG[C/T]TGAAAAGTTAATATT | 9873 |
rs115202509 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142640 | GTGGCACGTTCCAGA[C/T]GCCTCCTGCCCTCCC | 9873 |
rs115306402 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923916 | TGAAATACAGCTCTG[C/T]GTGACAGAGCAAGAC | 9873 |
rs115313998 | snp | C/T | 0.0217236 | 0.101931 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836295 | TCACACAATTCATTA[C/T]TCCTTAGGGTGGAGG | 9873 |
rs115330229 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095143 | GAAGTGTTCTTATTT[C/T]TTATTAATTAGGTGA | 9873 |
rs115373005 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003127 | GCAGGGAAACATATC[C/T]TGAACACTGATATAC | 9873 |
rs115382841 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916410 | TTCCAATTCCTGGGC[A/T]CAAGTAATCCTCCCA | 9873 |
rs115402459 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867262 | ATTTTTCTGGTACTT[A/G]GATCTCCAACATGAA | 9873 |
rs115410165 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889727 | TCAAATAAAACAAAA[A/C]AACACATATAGGATA | 9873 |
rs115419800 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969837 | TGGATGAAGTTTAAA[C/G/T]ACACACATTGGTTAT | 9873 |
rs115426147 | snp | A/G/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017548 | TCTCAAGTTCCTCCC[A/G/T]AACTTGGCAACAATT | 9873 |
rs115430925 | snp | G/T | 0.0150695 | 0.0854849 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901872 | CTATTCTGGTTTTTT[G/T]TTTGTTTGTTTGTTT | 9873 |
rs115461335 | snp | C/G | 0.0232847 | 0.105357 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838171 | AATACGAAGGACACT[C/G]TTATTTTAAGTCTGT | 9873 |
rs115470194 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098891 | CAAAAGCACAAACAA[C/T]GAAGAAAAAACAGGT | 9873 |
rs115480895 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848358 | TCTATACCTGCTGTT[C/G]TCTTTGCTTAGAAGG | 9873 |
rs115503432 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090519 | CGTGAGCCACCGCGC[A/G]CGGCCTACAATACTT | 9873 |
rs115538474 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950457 | TCAAAGAGTTTTATA[C/T]AGTTTTAGCTCTTAA | 9873 |
rs115550866 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927420 | GTCAGTGTAGGTTCA[C/T]CAATTGCAACAAATG | 9873 |
rs115584766 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982504 | GTTTTGGGAAAACAG[C/G]AAAGAATGACAGATA | 9873 |
rs115665885 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929694 | ATAAATATTTATATA[C/G]ACTTTGATTAAAAAG | 9873 |
rs115666265 | snp | A/C/G | 0.00875309 | 0.0656392 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093054 | AGGCTAAGGCCAGCC[A/C/G]CATGAGTAGTAATCA | 9873 |
rs115677815 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997875 | CTGGCTAATTTTTAC[A/G]TTTTTTGTAGAGACG | 9873 |
rs115701249 | snp | A/G | 0.00494653 | 0.0494853 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840999 | CATTTTACTTGAGTT[A/G]TTGAGCAATAATGCT | 9873 |
rs115702074 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928677 | TTGAATCTTATTTAA[C/G]TAGGTGAGAGGAGGC | 9873 |
rs115705219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028719 | TTGTAATCCCCATGT[A/G]TCAGGGGAAAAACCT | 9873 |
rs115708254 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126738 | ATACACAAAAAAGAA[A/C]ATACAATAAAAAGCT | 9873 |
rs115718387 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006551 | CTACCCCGCTTTGAG[C/T]CACCCTCACCTTATG | 9873 |
rs115721591 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018771 | CTGAGATTATGACCA[A/G]GTGGCTTTAATATAA | 9873 |
rs115721767 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106210 | CCAAGGAGTTCGAGA[A/C]CAGCCTGGGAACATA | 9873 |
rs115726258 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937653 | TGGCCAAAATATTTT[C/T]TTAGAACCTACTCTG | 9873 |
rs115736450 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953669 | TCTTAAATGTTATGG[A/C]AGGTTGTAATAAATA | 9873 |
rs115780798 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965848 | GCTCTACCTCATGAC[C/T]AGGATTAATCCATGC | 9873 |
rs115888856 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932509 | TATTACACCTTCTCT[A/G]CAATGCAGTTTTTGG | 9873 |
rs115894057 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878681 | TTGATAATATACTAA[A/G]TAGATAAAAATCTAT | 9873 |
rs115902490 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108268 | TTAGATCTTTTCCTA[C/T]GAAGTTGTTTAAGCT | 9873 |
rs115907550 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878525 | TCTGGGCAGGAAAAA[A/T]ATAAGGTGAACACTG | 9873 |
rs115930873 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980151 | ATCGTCTCTGTAAAT[G/T]AGGAAGAAAACCCAC | 9873 |
rs115933650 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132307 | AATGCTAAATACCTA[A/C]CATTCTTGGCATTTC | 9873 |
rs115942451 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125173 | AAATGATAACAGATG[A/G]AAACTCAAACCTGTA | 9873 |
rs115967958 | snp | C/T | 0.000927558 | 0.0215155 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983792 | AGTCATTATTTTATT[C/T]CTTACATCACTCTTG | 9873 |
rs115976304 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103088 | AAAAGTAAATCAGCA[A/G]TTATTTGAGGCTGAA | 9873 |
rs116002987 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123792 | TTTCTCTAGTTACAG[A/G]TGCTGGCCAACTGAC | 9873 |
rs116062710 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949587 | CTTTCTACATTTCTG[C/G]ATTTGCCTATTCTGG | 9873 |
rs116084245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960046 | CTGCTGTAAAGGAAT[A/G]TGTAAGGCTGGGTAG | 9873 |
rs116085316 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916606 | AAGCGTGAGCCACTG[G/T]GCCCAGCCTCCTTTG | 9873 |
rs116113806 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135843 | TGGTCTCCTCCCCTC[A/G]AAATTCCAAAAGATA | 9873 |
rs116118214 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997462 | CCACAATGTCCAATA[C/T]TGTGAGTCATAATCA | 9873 |
rs116210010 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841288 | ATGAGCCGTGATCAT[A/G]CCACTGAACTCCAGC | 9873 |
rs116210869 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928679 | GAATCTTATTTAAGT[A/G]GGTGAGAGGAGGCCC | 9873 |
rs116215431 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115256 | ACTCTCCCTCCCTGA[C/T]ATGCAGAATCTCCAC | 9873 |
rs116229484 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057754 | AGTCCCTAACCCTTT[A/G]AATCAGAGCTTCCCA | 9873 |
rs116233754 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043512 | ATACAACTTTTATTG[C/T]TGTCTTTAAAAACTG | 9873 |
rs116240892 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001634 | ACATTGTCTTTCAAC[A/G]ACATCATTTTACTCT | 9873 |
rs116241211 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924713 | AATACACAAATTCTG[A/T]CCCAAAAGCACTGAG | 9873 |
rs116245253 | snp | C/G/T | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914053 | AAGGAGTCTCACTGT[C/G/T]GCCCAGGCTAGAGTG | 9873 |
rs116295237 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020359 | TTTCATCCCTCAGCA[C/T]ACAGAGAAACTAATA | 9873 |
rs116322355 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041907 | TCCTAGGTTTAAGTC[C/T]AATCCACTTTGAGAT | 9873 |
rs116323406 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969123 | CAGACTCCAGATGTC[C/T]CCTCCTCATTGTCAG | 9873 |
rs116351371 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111329 | TTTACAACTGTTATA[A/T]CTTCTTGCTAAATTG | 9873 |
rs116352467 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124991 | TCAGAAATAATGAAA[A/G]CCAGAAGACACTGGA | 9873 |
rs116356495 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028117 | CAGGGGCACTGCCTA[A/C]TGGAGGGGTGAGAAG | 9873 |
rs116394852 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872260 | GGTGACAAAGACCTT[C/T]TGGCACACAACTTTT | 9873 |
rs116412856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061378 | ACAAACCTGGGTGGC[C/T]ATTTGGGCAAACACC | 9873 |
rs116417616 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989601 | AAGAGAAGCACGAAA[C/G]CTGGGTACCACATAA | 9873 |
rs116437116 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894680 | CTACACGTTTGTACA[C/G]GTTCACAATCCCACA | 9873 |
rs116526311 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015536 | TGTCACCTGCCTTCT[G/T]TAAGTTTCAATTGGG | 9873 |
rs116529002 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869533 | AATACTTGCTTTTTT[C/T]TTTTTTTAATAAAAG | 9873 |
rs116539912 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042416 | CATCCCATTGTTCTA[A/T]GTGTCTGTATTTATA | 9873 |
rs116591754 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840521 | TTATTTCATCTTGGT[A/G]TTCCTCAAAGAGGCA | 9873 |
rs116597116 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041624 | TACTGAGTTGAGTTT[C/T]TTATATATTCTGGAT | 9873 |
rs116615223 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019639 | TTATTCAAGTTAGTT[C/G]ACAGAGGCAGGAATC | 9873 |
rs116625556 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896316 | CCTGAGGAAGTTTCC[A/G]TGTTTTTCCTGCCTG | 9873 |
rs116626069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885799 | CTACTTGGCCAGCAC[C/T]CTAAGATAGTGGTTT | 9873 |
rs116667893 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130532 | TGCCTTGGGCTGCAA[C/T]GGCTGTCCCATTCAG | 9873 |
rs116726729 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054831 | ACAGACATGTGGGCC[C/T]GGTGGCATGTGCCTG | 9873 |
rs116727324 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073149 | GAGTACTGCAAATGA[C/T]TTTACCAACACCTCA | 9873 |
rs116749689 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903985 | TGAATAAGACAAACA[A/G]ACAAGGTTAGTATCT | 9873 |
rs116752266 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950855 | CTTCCTGGGCACATG[C/T]TGTGGGACTACACTT | 9873 |
rs116818176 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894732 | TGAAAAAGAATAAGT[A/T]TTTTTTGGTAAGTTT | 9873 |
rs116831617 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106319 | GCTAAGGCAGGAGGA[C/T]TGCTTGAGCCCATGA | 9873 |
rs116842217 | snp | A/G | 0.030278 | 0.119257 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060710 | AAAATGGGCATGAAA[A/G]TAAGATAACTATTTC | 9873 |
rs116845993 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954970 | GCTTTTTCTACCCTC[A/G]CTCACCACTCAACAC | 9873 |
rs116878858 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137148 | AGGCAACTGAAGTTA[C/T]CATGAATACCAAGAG | 9873 |
rs116884791 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839858 | GTAGATGAGGTCATT[C/T]GGCAAGAGTGCGTTC | 9873 |
rs116885891 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997159 | TCCAGTAGAGAACTA[C/T]AGCCGAGAGGCCAAA | 9873 |
rs116923077 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966459 | ACCACCACACCCGGA[C/G]TAAACTGAGCATATT | 9873 |
rs117002492 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097145 | ATAGCTAGAACTACA[A/G]GTATGCACCACCAGG | 9873 |
rs117005908 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128128 | AGGAGAATCCTAAGA[A/G]GCCAAAATACAAAAA | 9873 |
rs117006866 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035336 | GCACCACTACTCCTG[C/G]CTTGTATTTTTTGTA | 9873 |
rs117008121 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093333 | CAGTGAGCTCTGAGA[A/G]TCCTGGCAAATTATT | 9873 |
rs117021568 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848000 | CCCGGCCAACTCTAA[C/T]CATTAAATATAGTTT | 9873 |
rs117023160 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035148 | GTTTTTAGTTTTTAT[G/T]TTTATGTATGTATGT | 9873 |
rs117024108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895750 | TAACTGTCAGTATTG[C/T]TAATTCTAAAACGCA | 9873 |
rs117054606 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979146 | TATGGGTGTAAGTCA[C/G]CATGCCCGGCCACAG | 9873 |
rs117085272 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915956 | CTATCCTTAGCAAAC[G/T]AATGTAGGAACAGAA | 9873 |
rs117127779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907143 | CATTATTTGGCTCTC[C/T]ATTACTGCTGGAATG | 9873 |
rs117167659 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058223 | ATTATTGTTTTATGT[C/T]ATAAAATCAGCCAGG | 9873 |
rs117174420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046793 | TCACCATGTTGCCCA[A/G]GCTGGTCTTGAACTC | 9873 |
rs117181194 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074494 | AAATGTGAAATATTA[A/C]ACAATAAAAATTCCA | 9873 |
rs117191547 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888712 | TAACCTCCACCTCCC[A/G]GGCTCAAGCAATTCT | 9873 |
rs117218917 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080397 | TGTAATTCCACTGTA[C/T]CTGCATACATTCATA | 9873 |
rs117276035 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925661 | ATAACTGACGCACGT[A/G]TCCCAGGGTCCACCA | 9873 |
rs117279208 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937466 | ATGCTGGCCAATTTG[A/G]GTATTCCTTACATTG | 9873 |
rs117280763 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883215 | CACAAAGAAAAGCTT[C/G]AACTATAACACTTCT | 9873 |
rs117288769 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926938 | TGAAAAAAATGGCGA[C/T]TTGGTGCACTAGTAG | 9873 |
rs117298868 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930521 | CTTTGGGATCAGGAG[A/G]ATCACCTGAGGACAA | 9873 |
rs117308472 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070199 | GGAAAGCAATCTCCA[A/G]AACAATATCCCTATA | 9873 |
rs117331368 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966857 | TATAGTTTGAGGAAG[C/G]ATTCCCTAAAGAAGT | 9873 |
rs117337119 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858947 | AGGACAGTGATCCCT[C/G]GGGGATGGGAAACAA | 9873 |
rs117374082 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089586 | TATATTTATATAATG[C/G]AATGTTATTCAGCCA | 9873 |
rs117377192 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020902 | TACATTGAGACAGGG[C/T]CTTGCTCTGTCACCC | 9873 |
rs117386734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060908 | CACTATAGTGAGATT[C/T]CCGTGTTCATGAAGG | 9873 |
rs117395638 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876305 | GTCCAGCCTGCGAGA[C/T]AGAGTGAGATGGTCT | 9873 |
rs117437316 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094609 | TGACCACTTCATTTT[C/T]GCTACGATACTTGAC | 9873 |
rs117438589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029616 | TTGTGGAGGTGCAGA[A/C]ACAGAGGTAGGAAGT | 9873 |
rs117442324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964300 | ACATCGAATCATGTA[C/T]TATTGTCTTTGCACT | 9873 |
rs117466269 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981945 | ATGTTCAAGCCACTG[C/G]ACTCTAGCCTGTTAT | 9873 |
rs117484624 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845224 | CCAGCAGTTTGAGAC[C/T]GGCCTGGGCAACATG | 9873 |
rs117495951 | snp | A/T | 0.0327778 | 0.123752 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110098 | TTTGCTAGTATTTTG[A/T]GGAGGATTTTTGCAT | 9873 |
rs117512134 | snp | A/G | 0.0360663 | 0.129354 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838300 | CTTGGGGAGGAGCCA[A/G]CCTCTCCTGAAATCC | 9873 |
rs117527774 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102427 | AGGACCCATACACAA[A/G]TGTGTACAAAATGTG | 9873 |
rs117545018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870054 | TGTTCCTCTGATCCA[A/T]CATGTGCTTGCGTGC | 9873 |
rs117559934 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987071 | CAGTGTTTCCCAGGC[C/T]CTTCAGAATAAACAT | 9873 |
rs117590031 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058852 | GGATTACACGTGTGA[A/G]CCATCCCACCTAGAC | 9873 |
rs117591835 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078832 | CACGTGATTCTCCTG[C/T]TTCAGTCTCCAAGTA | 9873 |
rs117594886 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991561 | GCTGGTTCAACATAC[A/G]CTGATCAAGTGGGCT | 9873 |
rs117610694 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070209 | CTCCAGAACAATATC[C/T]CTATAAGTGTAGTCT | 9873 |
rs117617770 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971878 | TTGTTACATAGCAAC[A/G]GAAATCAAATATAAC | 9873 |
rs117624063 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051320 | ACTCTAGCTCTAAAA[A/G]ATAAAAAAATAAAAA | 9873 |
rs117631429 | snp | A/T | 0.0360663 | 0.129354 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72844141 | GCCATTTTCTGGAGG[A/T]TGTGAGTCAATGTGG | 9873 |
rs117645057 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994230 | GTACTCTGTCCTTCT[C/T]AGTAAACCTCTTGTC | 9873 |
rs117651646 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875562 | TCAAACTCCTGGCCT[C/T]AAACGATCCTTCCGC | 9873 |
rs117664896 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062601 | AGAACATAAATGACC[C/T]GATGGAGCTGAAATA | 9873 |
rs117678186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900480 | AAAAGTGAGATGAGA[A/G]TCACTGTTATTCTGA | 9873 |
rs117705747 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042549 | TATTGAGGTCTTCTG[C/T]GGTTCCATACAATTT | 9873 |
rs117707243 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031988 | AATATCCACCAAGAG[A/G]AACTATTAACTAAAT | 9873 |
rs117733068 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904704 | TTCTTTTTTTTACAA[A/G]AAAGTTTTTCAAATC | 9873 |
rs117794201 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071905 | TGACACATGATCTTA[A/C]TATATGTTCTTTAAC | 9873 |
rs117801487 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036226 | TTTTAAAGGAAGAAA[A/G]ATATACAATTAGAAA | 9873 |
rs117824058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130721 | AGACCCTCTCAAACT[A/G]TATTTCCTTCTCTGC | 9873 |
rs117893776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032940 | CAGTGCCATTATCAG[A/C]CTAAAATGTGATTTA | 9873 |
rs117932352 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913951 | AACAAATGAAAAAAC[A/G]TACTATGCTCATGGA | 9873 |
rs117943137 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986995 | CCTCAAAGCGAGATC[C/T]TGAGGCCCAAATTCT | 9873 |
rs117946797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015267 | GATATTAACTAGCCA[C/T]GTCTAAATCTTTTGT | 9873 |
rs117962776 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933582 | ATAAATGATACCCAA[C/T]TTATATTAGCCATAT | 9873 |
rs117969824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040251 | CAACCCAGCTCTTTT[C/T]CCAGGAACAGGAGAA | 9873 |
rs117972485 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130984 | ACATTTTAAGTTCTA[A/C]TTTGAAAGAATACTA | 9873 |
rs117980813 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998206 | AAGATTTTTATATTG[C/T]TCATGAGGTAGTAAA | 9873 |
rs117984489 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095646 | GCTCCAAAACTCAAA[A/G]CGGGAGTACCTTTGT | 9873 |
rs118010414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040539 | CATTCTGTTGGTGAT[A/G]CCTTCCCTTGTCAAT | 9873 |
rs118051917 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836265 | ATCCACCCCTGGGAC[C/T]GAGAAAATCTCCTTT | 9873 |
rs118071307 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997345 | CTAAAACCAGAGATC[C/T]TAACAGAATCAAGGT | 9873 |
rs118077937 | snp | C/T | 0.143284 | 0.226079 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853121 | TATAACAAACCTGCA[C/T]ATGTACTCTTGCACT | 9873 |
rs118109338 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006287 | TCCAACTTGGATATT[C/T]AGTAGGCACCTTTAC | 9873 |
rs118125226 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088641 | ATTCATAAACATGTA[C/T]ACACACTTTTTTTAC | 9873 |
rs118141553 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877870 | AATTAGCTGGGTATG[G/T]TGGCACATGTCTGTA | 9873 |
rs118152894 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017097 | AAACAATCCTCCCAA[C/G]TCAGCCTCCCAAGTA | 9873 |
rs118185214 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898822 | GCAACCTCCACCTCC[C/T]GGGCTCAAGTGATCC | 9873 |
rs137862963 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907841 | CTCGTCATCTGCCCA[C/T]CTTGGCCTCCCAAAG | 9873 |
rs137935783 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010262 | TTGGTTCTTTTTTAT[A/C]TCTCTCTTTGGTAAA | 9873 |
rs137950141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102749 | ATAATGCATCAAGAG[C/G]TTCCTCACCAGATGC | 9873 |
rs137962254 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089834 | ATTTTTATTTAACTA[C/G]ATAAGCATTTTCATA | 9873 |
rs137966433 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048465 | ACAACTCAAAAAGTG[C/G]AAATGGATTAAAACA | 9873 |
rs137971113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853231 | ACAAGGATGCCAAGA[A/C]CACTCAGTGGAGGAA | 9873 |
rs137979422 | snp | A/C | 0.144969 | 0.226867 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991008 | GAATCAAACAGACGC[A/C]ATAAAAAATGATAAA | 9873 |
rs137998102 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125484 | CCAAAGAAGGGGGAC[A/T]GCTTGAGCTCCACAG | 9873 |
rs138009125 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950249 | AATATTAAATCCTTT[A/T]CAGATATGTAATTTG | 9873 |
rs138010437 | in-del | -/AT | 0.040671 | 0.13668 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938670 | GTCTGGAGAGGGTCA[-/AT]TTTCATCATTCTTTT | 9873 |
rs138014563 | in-del | -/AATATCTGTTA | 0.0437281 | 0.141251 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126608 | AATACGAACTTTTAT[-/AATATCTGTTA]AATATCTGTTATGCT | 9873 |
rs138023210 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895271 | TATACCCATTAAGGC[C/T]GGGGTGAAGAAATGA | 9873 |
rs138050533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000689 | CTAATACACATCAAA[C/T]TATACCGATATTGTG | 9873 |
rs138085044 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941848 | GCTTCAAAAAAAGAT[A/G]TCTTAAGGAAGTTAT | 9873 |
rs138085724 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094793 | TGGAATACAGTGGCT[-/G]GTTTGTAAAGGTATT | 9873 |
rs138086578 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902711 | TTATAAAGTTTAAGA[C/T]TTATTCTGCTATTTT | 9873 |
rs138088346 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927423 | AGTGTAGGTTCATCA[A/G]TTGCAACAAATGTGC | 9873 |
rs138094995 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029930 | AAAACAAAAGAAAAA[C/G]AAAAACAAAAACAAA | 9873 |
rs138123962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883361 | CCAATCTAGAAAATG[A/G]AAAGGTAAGCCAAAG | 9873 |
rs138191331 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882672 | TGTACAATTATTTTG[C/T]ATCAATAAAAAATTA | 9873 |
rs138193944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846871 | ATATTAGGACATAAG[C/G]GTTTCTTCTTATATA | 9873 |
rs138227849 | in-del | -/TG | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935887 | TTTTTCTATAAAGCT[-/TG]TGTTATCCTCTTGCA | 9873 |
rs138232413 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065689 | AATCAATGTGCAAAA[A/C]TCATAAGCATTCCTA | 9873 |
rs138243522 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058588 | GTTTTTTAGGTTTAT[G/T]TCATTTTCCTTTTTT | 9873 |
rs138253386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913394 | ACACCTCAGCCTCCC[A/G]AGCAGCTGGGATTTC | 9873 |
rs138317587 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857676 | GCTGGTCTTGAACTC[A/G]TGACCTCAGATGATC | 9873 |
rs138320954 | snp | A/G | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867899 | CTGGTCACTGCAGGA[A/G]GGCGGGCCCATCGCT | 9873 |
rs138330211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022397 | AAACCTCATGGAACT[A/G]ATAACTGAGTTTAGC | 9873 |
rs138356958 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118260 | GCAGGCAGAGACTGC[A/C/G]GTGAGCCGAGACTGT | 9873 |
rs138364507 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954879 | ATATCTATACATATA[C/T]ACACACACACACAGA | 9873 |
rs138389902 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029345 | CACTGCGGCAAGATC[A/G]GTTTGATGCAATTAT | 9873 |
rs138400377 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104442 | GCCTGGCTAATTTTT[A/G]GATTTTCAGTAGAGA | 9873 |
rs138400995 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868246 | AGCAAACTAAGGCAG[A/C/G]AACAGAAAACCAAAC | 9873 |
rs138416817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039405 | TGCCTGTAGTCCTAG[C/T]TACTCCAGAGGCAGA | 9873 |
rs138425398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131544 | AAAAAAAATAAAAAT[A/T]ACTACAAAAATTATC | 9873 |
rs138432563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902921 | GAAAGCAAGAAGATA[A/G]TTTTTACACAAAAAG | 9873 |
rs138434576 | in-del | -/AG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869443 | TGGGGGGAGGGAAGA[-/AG]AGAGAGAGAGAGACA | 9873 |
rs138442949 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016874 | TATAACAGGTGTCAG[A/G]GAGAGGTACAGGGAT | 9873 |
rs138446983 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107911 | CTGCAATCGACATGG[A/G]TATCTTTTGGATATA | 9873 |
rs138451046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976483 | CAAAGTCTCACTATG[C/T]TGCCCAGGCTGGTCT | 9873 |
rs138452684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873502 | TATCAGATACATGAT[G/T]TGCAAATATTTTCCC | 9873 |
rs138471526 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955018 | ATGTGTGGGGACTTT[C/T]CCACATGCCAAGCAA | 9873 |
rs138480712 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962173 | TCTGAGACCCTTTTA[A/G]GGGACCTGTGGGGTC | 9873 |
rs138484535 | in-del | -/ACACACACAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999867 | TTTCTGCACAATCAG[-/ACACACACAC]ACACACACACAAACA | 9873 |
rs138487138 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060072 | GGTAGGATACACTGC[A/T]ATCAGAGATGACTAA | 9873 |
rs138510554 | in-del | -/A | 0.385741 | 0.209939 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078649 | ATAAAAAAAAAAAAA[-/A]GTACTGGTTGCCATT | 9873 |
rs138526473 | in-del | -/TTTG | 0.109108 | 0.206518 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923157 | TCAGTTGTACCACAT[-/TTTG]TTTATTAATCAGGTG | 9873 |
rs138562468 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098914 | AAACAGGTAAAATGA[A/G]CTTCATCAAAATTTA | 9873 |
rs138622197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124819 | AAAGCATCAACCATT[A/G]AATGATGAACCCCAA | 9873 |
rs138634237 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141466 | CGGCTGGAGGGCTCA[A/G]AGCTGGTGCAGACTA | 9873 |
rs138638149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995229 | TTTATCTTGCAGAAC[A/G]AAAAGCTGTTTTCCC | 9873 |
rs138653886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083119 | TAAAGAAGAATAAAT[A/C]AACAAACTTGTAAAA | 9873 |
rs138656618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978435 | AGGTGCTCAATATCA[C/T]TGACCATCAGAGAAA | 9873 |
rs138657916 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074890 | GCACTCCAGCCTAGG[C/T]GACAGAGTGAGACCC | 9873 |
rs138664316 | in-del | -/TA/TATA | 0.118021 | 0.215066 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107035 | TTTTGTTAGAAAAGC[-/TA/TATA]TATATATATATATAT | 9873 |
rs138669194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839561 | GCGAGCTCTCTGCAA[G/T]GTATACCTGGCAGGA | 9873 |
rs138725034 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942535 | ATGCCTAGGAAAGAT[G/T]AGAAGGATATGCCAA | 9873 |
rs138728187 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034727 | ATTTGCACAAAATGA[C/T]CTGCAAATTTTAAAG | 9873 |
rs138758312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932982 | CAAGTTAAAGGAGTA[A/G]TTGATTTCATAAAAC | 9873 |
rs138765855 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876752 | TTCTATCAATTACTG[A/G]AAGAGGGATCCTAAA | 9873 |
rs138767346 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848070 | CTGGACTATAAGAAT[G/T]ATGATTAGGCTTAAA | 9873 |
rs138791840 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948231 | CAGGCTGGTCTTGAA[C/T]TCCTGGACTCAAGCA | 9873 |
rs138797316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852793 | ATGTGGTACATATAT[A/G]CCATGAAATACTAGG | 9873 |
rs138821268 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021452 | CTTAGCAAACTAATG[A/C]AAGAACAGAAAACTA | 9873 |
rs138825787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114285 | AGTGCTCTTCAGTCA[C/T]CTTGTGGTGAATTCT | 9873 |
rs138831216 | snp | A/G | 0.000164275 | 0.00906148 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867924 | ATCGCTCATTTTCCA[A/G]TTCTTCCATTACTTG | 9873 |
rs138847212 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881870 | GCTGGGGCCGGGTGC[A/G]GTGGCTCACGCCTGT | 9873 |
rs138856854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839004 | AAATGTTGTGAGCAC[A/G]TGCTTTCAACCTAGT | 9873 |
rs138878062 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863317 | AGGGACAAAGAACTC[G/T]GACTTATTCTGTTTA | 9873 |
rs138884204 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055452 | AGAGCTCTTTATCAG[A/G]AGAAGTATACAATGA | 9873 |
rs138909479 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963559 | AAAAAATGTGGATTG[G/T]ATCAGCAGCCCCCAA | 9873 |
rs138979720 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061124 | ACCTGGTTCATCTCA[C/T]TGGGACTGGTTGGAC | 9873 |
rs139013046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013127 | GCAAACTCTATACTG[C/T]GATATGTAAAGTCCT | 9873 |
rs139013123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908660 | GTACCTTTCCATATG[A/C]CTGTCTGCCACTTAT | 9873 |
rs139019742 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016352 | CAACCAACCAACCAA[A/C]CAAACAAAAAACAAT | 9873 |
rs139021724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912795 | TATTACAGCTTTGAT[C/G]TTGTTACTTGTTTTT | 9873 |
rs139024112 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078632 | AAAATAACAACTATT[C/T]TGATAAAAAAAAAAA | 9873 |
rs139052840 | snp | C/G/T | 0.000171153 | 0.00924944 | synonymous-codon, missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72902567 | GTCACAAGGCTGGAA[C/G/T]TGGAAGGGCTGGGGT | 9873 |
rs139075918 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971093 | GTATAGACTTGAAGG[C/T]AAACTAAATGCTGTT | 9873 |
rs139077318 | in-del | -/AT | 0.153 | 0.230415 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887076 | TATATATATATATAT[-/AT]GAATATATGTCTCCA | 9873 |
rs139080054 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066305 | GCCATATGCAGAAAA[C/T]TGAAACCGGATCCCT | 9873 |
rs139093689 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073821 | AATAATAAAAACTGT[A/G]CATGTGCAAGGATTT | 9873 |
rs139096262 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933149 | AACTTGCAGGGTAGG[C/T]AGATATGCAAGACAG | 9873 |
rs139096647 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116642 | AAATCCTGGGCACAA[C/G]CTCCCGCGTCAGCCT | 9873 |
rs139135376 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069934 | ATATGTAAAAAAACA[A/G]AGTCACAGAAAATTA | 9873 |
rs139154031 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917610 | CGAAGACTGGGCCGA[A/G]TGCAGTGGCTGACGC | 9873 |
rs139157139 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031080 | GTATGAATCTGGATG[A/G]GTTCATCCAGAATAT | 9873 |
rs139159296 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119952 | ATTGGACTTACAGTT[A/C]CACATGGCTGGGGAA | 9873 |
rs139161872 | snp | C/T | 8.4016e-05 | 0.00648081 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841539 | AGGCTGGTCGTACAA[C/T]GGCAGTGGAGGCAGG | 9873 |
rs139167869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018139 | CTCAAATTGTCACAT[C/G]TGTGGTCTGTCAGAG | 9873 |
rs139214762 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972351 | AGACCTCTATAAGAA[A/G]TTTGGTAGTTGGAAA | 9873 |
rs139241556 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109438 | TGCAGAGATCTTTCA[C/T]TTCATCAGTTAATTC | 9873 |
rs139242866 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082368 | AAAAAAAAAAGAAAA[A/G]AAAAAGCATTCAACA | 9873 |
rs139250745 | in-del | -/AA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133814 | AAAAAAAAAAAAAAA[-/AA]GTAACCATTATGCCA | 9873 |
rs139268471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959311 | CTCGGCTCACTGCAA[A/G]CTCCACCCCCCAGGT | 9873 |
rs139271142 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879148 | ACAAAAAAAAAGATA[C/T]TACAACTCTATCCAG | 9873 |
rs139273875 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056526 | CTTTGCTAAAATGAA[C/G/T]CAATTTAATCTTTCA | 9873 |
rs139282498 | in-del | -/ATA | 0.499 | 0.0223418 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890387 | TAAGAACAAAACAAT[-/ATA]ATAACAGCAACACAA | 9873 |
rs139290743 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133742 | AGGTTACAACGAGCC[A/G]GCATCGCGCCACTGC | 9873 |
rs139295729 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872287 | TTTTTTTTTCTTTTC[-/TT]TTTTTTTTTTTTTTT | 9873 |
rs139333874 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978960 | CTCTCAGGTTCAAGC[A/G]ATTCTCGTGCCTCAG | 9873 |
rs139386488 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997726 | TTTGTTTTGAGAAAG[G/T]GTCTCCCTCTGTCAT | 9873 |
rs139395844 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127468 | TGTGCCTAGATCCCT[A/C]ATTAGTTACTGAAAA | 9873 |
rs139404812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897504 | GTTATATGCAAATAT[A/T]ACATCATTTTATATA | 9873 |
rs139411354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841073 | TTTGGGATACTGAGG[C/T]GGGAGGATTACTTGA | 9873 |
rs139419717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980171 | AGAAAACCCACTTGC[A/T]AAGCATAAAAGAGAA | 9873 |
rs139451596 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031418 | GAGGTGGAGGCTGCA[C/T]TGAGTTGTGACTACT | 9873 |
rs139490055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884957 | AATAATGAGGACTCA[C/T]ATTTTATATAACCAG | 9873 |
rs139492265 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096870 | TCCATTCCTAGTTTT[C/T]TGAGTCTTTTTATCA | 9873 |
rs139508122 | snp | A/G | 0.0248432 | 0.108648 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144440 | GAATAGCGTGAACCC[A/G]GGAGGTGGAGCTTGC | 9873 |
rs139515863 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884286 | AAAGCCAGTATTGCA[A/G]AATATAATAGTTGAA | 9873 |
rs139520391 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096551 | GCAAAGGAAAGGAAA[G/T]GAAAGGAAAGGACAG | 9873 |
rs139525599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025574 | GTGATGCAATAATCT[G/T]TACCACAACCCCCGA | 9873 |
rs139527982 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983973 | TATATTCCAATGAGA[C/T]GCAACATAGCCTGGC | 9873 |
rs139557221 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889708 | ACAGAGCAAGCCTCT[G/T]GTCTCAAATAAAACA | 9873 |
rs139562774 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115978 | ACATAAAAGTAACCA[G/T]CACAGGGGCACAACT | 9873 |
rs139568627 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005310 | CAAATCAGACTTTAG[C/T]GTCTACCACTCTTCT | 9873 |
rs139588609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865134 | ATGTCTAACAGTAGT[A/G]TTAATCATGTTTTCC | 9873 |
rs139588810 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099735 | TGGGGCTGTCAAGCC[A/G]GACCAAAAAGGCTGT | 9873 |
rs139631736 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013773 | TAGCCTAGGAGCATA[C/G]CTTTTTAATCCTTAT | 9873 |
rs139638060 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945452 | ATAAAAACCCTAGAA[G/T]AAAAGCTAGGCAATA | 9873 |
rs139647968 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939639 | TTTTTTTTTTTTTGA[A/G]ACAGTGTCTCGCCCT | 9873 |
rs139661814 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854462 | TTAGAGACAGGGTCT[C/T]GCTCTGCTGCCCAAG | 9873 |
rs139669483 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110477 | CAATTTATTGGTATA[C/T]AGTTGTTCATAGTAC | 9873 |
rs139673303 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869430 | GGAAAGAGAGGGTTG[C/G]GGGGAGGGAAGAAGA | 9873 |
rs139679700 | in-del | -/AGG | 0.0134861 | 0.0810011 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882418 | GAAGGATTATGGGGA[-/AGG]AGAAGAAGAGAGATT | 9873 |
rs139693098 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138320 | TGACTGCAGTGTCCA[C/T]ATTCTTGACCATAAG | 9873 |
rs139716607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014349 | GCCCAGTCTAGTCTT[C/G]AACTACTTGCCTCAA | 9873 |
rs139718830 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104860 | ACCGTGCCTGGCCAA[C/T]TTTACTAATTGAAAG | 9873 |
rs139719199 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951400 | TGATAACACAGCAAA[C/T]GAGAGCGACAGATTA | 9873 |
rs139724091 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959737 | GGAGCAATAGAAGTA[C/T]TTAATATTAAATGTC | 9873 |
rs139731234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952208 | TTCTCTATCTTAATA[C/T]CAGAAAGATATATAT | 9873 |
rs139731860 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115489 | TGAAAACAATCTTAT[A/G]TATCTTTTCCAACTC | 9873 |
rs139732100 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057581 | ACATCTATATAAGGA[A/G]TATTCTACCTCCTTC | 9873 |
rs139791467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965896 | TAAAACAGAACACAA[C/T]ACTGGAGGGGAAATG | 9873 |
rs139836028 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071122 | TATTTTACAAGAACA[C/T]TTTTGGAAGACACAG | 9873 |
rs139843152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077170 | TCGTTCTACTTTCAC[A/G]TATGTTTGAAAACTT | 9873 |
rs139844164 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979823 | AAGACATATAGGAAG[A/C]TCTCAGGATAAATAC | 9873 |
rs139864836 | in-del | -/C | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114996 | CAGCACAAAGACTTG[-/C]CTAAGAATTGGAGTC | 9873 |
rs139877831 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921726 | AAATTTGTTCGTTAA[C/T]GCATTCTTCTAATAT | 9873 |
rs139904240 | in-del | -/A | 0.0912534 | 0.193131 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979493 | AACTTCTAAAAAAAG[-/A]AAAAAACAAACAATT | 9873 |
rs139907370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859778 | GCTAGGGCTAGAAGC[A/C]CTAAAAAGGATTAGG | 9873 |
rs139932333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099246 | ATGAGGTACTACTTC[C/T]TACCCACTAGGATGG | 9873 |
rs139942011 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030923 | TCTCTATACTTGCGC[A/G]TCCTGAATTTCTGCT | 9873 |
rs139946654 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045962 | AAAAAACATCTCTTG[C/T]TTATATTTCTACAAT | 9873 |
rs139952715 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085472 | GACTGAAATGACTTT[C/T]GGAGGATTTAAAGAA | 9873 |
rs139969359 | snp | G/T | 1.66308e-05 | 0.00288359 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840931 | TGATGCCTGTGAGAA[G/T]CCTGGTGACTCAGCA | 9873 |
rs139978371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944271 | AATAAACATAATCCA[A/G]CATATAAACAGAACC | 9873 |
rs139990700 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890543 | GCTAGATCAAATGAT[C/G]ACCAAGGGTTTCTTC | 9873 |
rs140047600 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047584 | TGAAATAAAGTATTA[A/T]CCTATCAAATAACAT | 9873 |
rs140054772 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050454 | TACTATAAACATATA[C/T]GGGACGGGTCACCTT | 9873 |
rs140058120 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144139 | TCCTCACTTGTAAAA[C/T]GGAGGTATAATGCTA | 9873 |
rs140087490 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899417 | TTAGTCATTAGGGAA[A/G]TGCAAACCAGAACCA | 9873 |
rs140088581 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998471 | CACCTGAGCCCAAGA[A/G]GCAGAGGTTGCTGTG | 9873 |
rs140101651 | in-del | -/GAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846092 | AGATAGATAGATAGA[-/GAT]TAAGTAGTTACGATT | 9873 |
rs140103402 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033856 | TTAACAACTAGTATA[C/T]TGTATTTACCTATTT | 9873 |
rs140132918 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090874 | CCTCTAATTTCAAAC[G/T]TTTTCATCACCCCAG | 9873 |
rs140144850 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095181 | CGAGTTAACTTTCCT[A/G]ACTGTGCTTCAGTTT | 9873 |
rs140145201 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934594 | TTGCCTCGGCCTCCC[A/C]AAGTGCTGGGATCAC | 9873 |
rs140145919 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906921 | GGCTCTTTTTCGGTT[A/C]CATATGAACTTTAAA | 9873 |
rs140146646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003926 | AGCCTGGCCAACACG[C/G]TGAAATCCCGTCTCT | 9873 |
rs140146837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036785 | GTCTTCCTCCACAAA[C/T]ATTGTGTTCACTCAT | 9873 |
rs140147424 | snp | C/G | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842427 | AAGATGGAGGTGTGG[C/G]AGGATGGCCACATTC | 9873 |
rs140147529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904015 | TGCAAAGAATTTATA[A/C]TCTGGGAACTGGGCG | 9873 |
rs140160021 | snp | A/G | 0.031825 | 0.122064 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009326 | ACATGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 9873 |
rs140178229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849617 | AGCCTAAACTCATCA[C/T]CATTCTGTTATGTTG | 9873 |
rs140212338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039722 | TTCATTATCAAGGAT[A/G]ACGAATGATGCAGGA | 9873 |
rs140212673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853122 | ATAACAAACCTGCAC[A/G]TGTACTCTTGCACTT | 9873 |
rs140213795 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939922 | CATGCCTGGCCTTGA[A/C]GGCTCTTTGTATAAC | 9873 |
rs140228039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019847 | AAAGGTTTACTTACA[C/T]AGAAAACAAAATCCA | 9873 |
rs140230474 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112807 | GCATACACTATCATG[C/T]CTGGCTAACATTTAT | 9873 |
rs140250816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862295 | CCAAATAGGAAAGGA[A/G]TAAGTAAAACTGTCT | 9873 |
rs140255342 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961474 | TTGCCCAGGCTGATA[C/T]TGAACTCCTGGCCTC | 9873 |
rs140260667 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026871 | CGCTCTCTCTCCTGC[A/G]ACCATGTAAGACATG | 9873 |
rs140262262 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969327 | TTTGGCTTTAAGTTA[C/T]TTATATCAGGAATAA | 9873 |
rs140264980 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836522 | TCCCATGGGAAAAGC[A/G]AAGACCGTAACCTAT | 9873 |
rs140272859 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090295 | CAGTGGCGGGATCTC[A/G]GCTCACTGCAAGCTC | 9873 |
rs140280382 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987222 | TTAACTTCCCCTTCC[-/C]TGATCTTCCTCCTTA | 9873 |
rs140283903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865769 | GGAGTGGGAATCTCA[C/G]AGTCTTTTAATCTTT | 9873 |
rs140324220 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933735 | TCTCAAAGCTTAAAG[C/T]AGACAATTTTTATGT | 9873 |
rs140378749 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840680 | CAGTGAAAAAAGTTC[C/T]AGTGTAGATTAAATG | 9873 |
rs140380444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038908 | ATAAATTATGACATG[C/T]CTCCCACTTTAGTGT | 9873 |
rs140380718 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097848 | ATATTTACTCTGTCT[A/G]TCTATTTTAGAGACA | 9873 |
rs140386400 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860129 | TGAGAATCTAATGCT[A/G]CCTGCTGGTCTGACA | 9873 |
rs140389692 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938766 | CACAATTTTCATTAA[C/T]AGAATAGTTCAGTTC | 9873 |
rs140393712 | snp | C/T | 0.000125276 | 0.00791343 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72889839 | CTTACCCGTTGTTGG[C/T]GAACAATGTTTTTAT | 9873 |
rs140405680 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845386 | GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG | 9873 |
rs140445702 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124518 | CCCAGCACTTTGGGA[A/G]GCCAAGGTAGGTGGA | 9873 |
rs140484268 | in-del | -/G | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989910 | AAGCTCAGCAAAGCA[-/G]GAGGAGACACTGGTG | 9873 |
rs140486256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994896 | AAGTATACAATTCAG[C/T]GGTGACAAGGTTGTT | 9873 |
rs140502810 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091943 | AGGAGGCTGAGGCAG[A/G]AGAATTGTTTGTACC | 9873 |
rs140511235 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886355 | CATAAGTCTGTGCTA[C/T]CCCCTTTTCTCTGAC | 9873 |
rs140545626 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118147 | AACATGGTAACACCC[C/T]ATCTCTACTAAAAAT | 9873 |
rs140551501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065613 | TTAGAAAACCCCATC[A/G]TCTCAGTCCAAAATC | 9873 |
rs140556226 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063364 | GAACATCAACACTAT[A/G]AAGAAACTGCATCAA | 9873 |
rs140557765 | snp | A/C/G | 0.000305991 | 0.0123655 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867866 | AAAAGAAATCGTACC[A/C/G]AGTGTAAAGTGCCAT | 9873 |
rs140561459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936068 | ACTTTCATTCAAATC[C/T]CAGTTCTACCACTTA | 9873 |
rs140568204 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014900 | CCAGGCTGGAGTGCA[C/G]TGACATGATTTCGGC | 9873 |
rs140570012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067702 | CACAGAGAAAATGAG[C/T]GGAATGAAAAAAAAC | 9873 |
rs140572677 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970197 | TTGAACAGATAATAC[A/G]TATACCACTTCCTTT | 9873 |
rs140633743 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017281 | ACCAAACCTGGCCAA[C/T]GTATTACTTTTGGAT | 9873 |
rs140695121 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062930 | TCAAATTCAGGAAAT[A/C]CATAGAACACCACAA | 9873 |
rs140697681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016656 | TGAAGTAGACAGATA[C/T]ATACTGGCATGTAAA | 9873 |
rs140718366 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107204 | GGATTACAGGCATGC[A/G]CCACCATACCCAGCT | 9873 |
rs140736128 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872180 | TTGGTAAATACTCTT[A/G]CAAAAATCTGCTTAT | 9873 |
rs140747098 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016132 | ACATGGTGAAAATCT[A/C]TCTCTACCAAAAATA | 9873 |
rs140752948 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954352 | TAGCTGGGACCACAG[A/G]TGCATGCCACCATGC | 9873 |
rs140771439 | in-del | -/A | 0.47726 | 0.104176 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897320 | TTTTTTAAAAAGAGT[-/A]AAAAAAAAAAAAAAA | 9873 |
rs140782014 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064787 | TCCTTGACACATACA[A/C]CCTCCGAAGTCTAAA | 9873 |
rs140783978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969453 | AAACACTGAGAGGGA[A/C]AGAGACAAAAAGATG | 9873 |
rs140817195 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914054 | AGGAGTCTCACTGTC[A/G]CCCAGGCTAGAGTGC | 9873 |
rs140830158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101389 | TAACTCTGTACTGAG[A/G]TGGGAACTACTGAGG | 9873 |
rs140848228 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912237 | AAATCTTAGAGGAAA[C/T]GCATTCAGTTTTTCT | 9873 |
rs140891884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894053 | TTTAACTCTGTAACT[A/G]AAATATAACCATTTC | 9873 |
rs140926660 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133367 | GTAGAAACAACCCAT[A/G]TCTCTGTCAACTGAT | 9873 |
rs140930483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081835 | AACATATATAAAATA[C/T]TCAGAGCATGGTACA | 9873 |
rs140940361 | in-del | -/TTG | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041593 | ATTTATGGAGTTTTT[-/TTG]TTTGTTTGTTTGCTA | 9873 |
rs140968315 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994436 | GTAGCAGTGATCCCA[C/T]TAAGATGAGAAAATA | 9873 |
rs140971021 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091419 | CCAGGTGTGGTGGTG[A/G]GTGCCTGTAATCCCA | 9873 |
rs140985202 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137163 | TCATGAATACCAAGA[A/G]GAGGCAAGTTTCAAC | 9873 |
rs140999225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935280 | TTTGATGTAATTTCC[C/T]CTAAAGTAAGAACTT | 9873 |
rs141005370 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068812 | TCATCTCTACAAAAA[A/G]TAAAAAAAAAAAAAA | 9873 |
rs141027363 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135256 | CACAGATACAGGGGA[C/G]AGTACAGTAGTATGG | 9873 |
rs141040331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073401 | CAACTTGAAAAAGTT[C/G]ACTGCTTGAATTCCT | 9873 |
rs141046332 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021085 | GTCTCGCTATGTTGC[C/T]CAGGTTGATCTGAAC | 9873 |
rs141105155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929384 | TTACCACCTCTGCAA[A/G]GCTGTGATACTCATT | 9873 |
rs141143422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895764 | GCTAATTCTAAAACG[C/T]AACACTCATGTCTTT | 9873 |
rs141144931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138726 | CAATTCTCTGCCTCA[A/G]CCTCCTGAGTAGCTA | 9873 |
rs141145006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087992 | TCAAGTGATCCTCTC[A/C]CCTCAGCCTCTTAAA | 9873 |
rs141187345 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044598 | AAAGTCACTCATAAA[A/T]CTTAATTCTATTAAT | 9873 |
rs141199608 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102488 | CTGAAAGCAATGAAA[C/T]GAAACATCCATCAAC | 9873 |
rs141200549 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941304 | TGAATTAATGAATGG[C/T]CTCAAATAAAAACCT | 9873 |
rs141204574 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042771 | TTGTAGGTCTTTCAT[C/T]TCCTTGGTTAAATTT | 9873 |
rs141223001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135880 | GGGGATTAAGGGGTG[C/T]GTTGCAGCAGTAGTG | 9873 |
rs141231810 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119781 | TATACAATATTTGAC[C/G]CATCAATTCTACTTC | 9873 |
rs141250039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888988 | TTGAGACAGAGTCTC[A/G]CTGTCGCCCAGGTTG | 9873 |
rs141266427 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068064 | ACTTATTCACTACCA[C/T]GAGAACAGTATGGAA | 9873 |
rs141275823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892536 | AATGTTCCAATACCA[A/C]CTTCACTATCAAAGA | 9873 |
rs141289190 | snp | A/G | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72989000 | TCTCGTACTGCATGA[A/G]CCATCTGTTCAGTCT | 9873 |
rs141309534 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838697 | TTTTGCTCTGTTCAA[A/G]AGTCATCATCATGCA | 9873 |
rs141315742 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106778 | TCAGTACAGTAACAT[G/T]CTGGACAGGTTTGTA | 9873 |
rs141317479 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948828 | CCGCCACTACGCCTG[A/G]CTAATTTTTTATATT | 9873 |
rs141380977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052493 | TTAAAGGCTAATGCA[A/G]TGTATTAGAGAGTAC | 9873 |
rs141383130 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953821 | GAGTATCGAGTTCTG[C/T]GGCTCTCTGGCATTA | 9873 |
rs141394612 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117312 | GTGGAGAACTAAGAA[C/T]TCACAATCAGGCAAT | 9873 |
rs141411173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034401 | ACAAACATGCAAAAA[C/T]GTTCCTCTTCCTGAA | 9873 |
rs141420513 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017069 | CTCAATGCAGCCTCA[A/C]CTTCCTGGGCTCAAA | 9873 |
rs141423275 | snp | A/G | 5.3934e-05 | 0.0051927 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73001122 | AAAAGATTTCCAAAC[A/G]GGATACATGCTCCTA | 9873 |
rs141441544 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874602 | TTAATTGCTGAAGCA[A/G]AAAAGAGAGAAGTAT | 9873 |
rs141531486 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104285 | ACTTATTTATTTATG[C/G]AGACAGAGTCTCACT | 9873 |
rs141551349 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913216 | TGATGAGATTTGGGT[A/G]GGGACACAAATCCAA | 9873 |
rs141562392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951379 | TATGACAAAACATCT[A/G]GCATATGATAACACA | 9873 |
rs141571649 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954222 | TTTTTTTTTTTTTTT[-/TT]GAGACAGGGTCTCAC | 9873 |
rs141591305 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048971 | GAGCTATGAAGAACA[A/G]TAAATATTTAAATAA | 9873 |
rs141617677 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943879 | GTAAACTACTACACT[A/G]AGAACGTATGAAGAT | 9873 |
rs141619117 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080696 | CACCTGTAATCTCAG[C/T]ACTTTCGGAGGCTGA | 9873 |
rs141677196 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083568 | AAAAGAAAAAAAAAA[A/C]AACAAGAAAGAAATA | 9873 |
rs141698014 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093476 | TTCTCGAACTTACAG[C/G]TGGTGTCAGAATTGA | 9873 |
rs141722119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937664 | TTTTTTTAGAACCTA[C/T]TCTGTGCCAAGAACT | 9873 |
rs141729582 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039238 | AGAACCTAACTTTCT[A/G]CAGGGTGCAGTGCTC | 9873 |
rs141731801 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076766 | AGCTATAAATGAACA[A/G]ATTTTGTAATGTATT | 9873 |
rs141731947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924898 | TATCAGGACATACTT[C/T]TCCTGAACTTGTTTA | 9873 |
rs141734054 | snp | A/C/G | 0.00795819 | 0.0626103 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028840 | AGCACTTCCCCTTTC[A/C/G]TTCTCTCCGTCTCTC | 9873 |
rs141746971 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030936 | GCGTCCTGAATTTCT[A/G]CTATTTTTTATCCTT | 9873 |
rs141759129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034743 | CTGCAAATTTTAAAG[C/T]AAAAGTAAATAGAGC | 9873 |
rs141791908 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933044 | AGTGGCATCCTTTTA[C/T]GTGGAATTCCAAGAC | 9873 |
rs141799406 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930262 | TGCCGAAACAATCTG[C/T]TGTGACTCTAAGACT | 9873 |
rs141804603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877587 | AAAGTCTCTTAGAGA[C/T]ATATTTATTCTACAT | 9873 |
rs141804665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936921 | AGTAAGTCCAATGTA[C/T]GGACTTCCTTGGAGA | 9873 |
rs141811726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873044 | ATTAATGTTACAAAT[A/C]TTAGGCCAGGCACGG | 9873 |
rs141828520 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983015 | AATAAAAGAAAGGGG[C/T]CGGGCGCGGTGGCTC | 9873 |
rs141849544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061951 | CCCAGCACTGTGTTC[A/G]AGCTCTGTGAAGGGT | 9873 |
rs141861044 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927137 | TAGGCAAAAAACCCT[C/G]TAAGCCTTTAAGGGT | 9873 |
rs141870443 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883111 | TGTATAGGAAAAAAC[A/G]AAACAAAACAACAAC | 9873 |
rs141878044 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909181 | GTCTGGGATTGCAGG[C/T]ACACGCCGCCACGCC | 9873 |
rs141914231 | snp | A/G | 2.15924e-05 | 0.00328569 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841549 | TACAACGGCAGTGGA[A/G]GCAGGGAGGCGTGTG | 9873 |
rs141942027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932561 | GCCTCTGAGCTTTCA[C/T]ACAGGCTTTTCTTCT | 9873 |
rs142022530 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098968 | CCTATAATCTCAACA[C/T]TTTGGGAGACTGAAG | 9873 |
rs142040552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126902 | AATTTGCCGAGCATC[A/G]TGTTGCACACCTGTA | 9873 |
rs142059365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036377 | TACAATATTTCACAA[C/T]GTTATATCGGTCTTT | 9873 |
rs142063236 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979950 | GTAAGAACAGAATGT[C/T]CAGGAAATACGAAAA | 9873 |
rs142064444 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880203 | AAAGAAATTGAAGAG[A/G]ACAAAAACGAATCCA | 9873 |
rs142066704 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055653 | ATGTTACAAATATAT[A/G]TATCACTTAAATTTT | 9873 |
rs142085324 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902728 | TATTCTGCTATTTTC[A/T]ATACAAATGAGAAAT | 9873 |
rs142104148 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112617 | TCCTCTTTAAGGTCA[A/G]TAACTCTTAGATTTG | 9873 |
rs142130423 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061270 | GCCTGAAGAACTCTG[A/G]AACAGATACTGTGCT | 9873 |
rs142135014 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059259 | CACTGTGTGAACTAC[A/G]GTTTATTTACCCTCC | 9873 |
rs142144574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013478 | CTAGCCTCTCTAATC[C/G]TAAGGTCTACTTTAA | 9873 |
rs142155723 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002331 | ATTTAGGCAGAGGTG[C/T]ATCACTATTCCTTTG | 9873 |
rs142166708 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971718 | CCCCAGAATCTCCAG[A/G]TAAGAATGCAGCCAA | 9873 |
rs142195604 | in-del | -/C | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856307 | CAGGATATGATGAGT[-/C]CAAAAGTACAGGCTG | 9873 |
rs142197813 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854280 | GATATTTGTAAACAA[A/G]TGTTCACAGCCACAT | 9873 |
rs142199416 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914556 | ATAGACCAATGAAAC[A/G]GAATAGAGAACCCAG | 9873 |
rs142233360 | in-del | -/GA | 0.115788 | 0.21092 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908343 | TGCTGCAATCAACAT[-/GA]GAGTGCAGATATCTC | 9873 |
rs142236923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051352 | TTTAAATCTGAGAAA[A/C]TGTAAGCATATTTTC | 9873 |
rs142241169 | snp | C/T | 0.000106061 | 0.00728145 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841458 | AGAACCCTTACCGTT[C/T]GCTGAAGGAGACCGG | 9873 |
rs142265247 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852502 | GAAACCTTGTCTCTA[C/T]TAAAAATACAAAAAT | 9873 |
rs142266887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947499 | GGAATTGACCACAAG[A/G]TCTTATTCTAAGCAA | 9873 |
rs142288080 | in-del | -/GT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088459 | TGATTGTATACATAC[-/GT]GTGTGTGTGTGCGTT | 9873 |
rs142302248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858964 | GGGATGGGAAACAAA[C/T]AAACTCCTACAACAT | 9873 |
rs142335433 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907887 | CGTGAGCCACCATGC[C/T]TGGCTGGTTTTGTTA | 9873 |
rs142372915 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096423 | AGATGTGGTGGCGGG[C/T]GCCTGTAATTCCAGC | 9873 |
rs142380262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041087 | ATGGCTAAATAGTAT[A/T]CCATTGTGTATATAA | 9873 |
rs142394697 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033301 | TCAAAAAAAAAAAAA[A/T]AGTAGTTAGACTACA | 9873 |
rs142402738 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940537 | GAGCTATGGAGAAAG[A/G/T]AGTAGTCTCATGTCA | 9873 |
rs142409479 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885567 | GAGGTTTCGTGGAGT[C/T]AGGGTACCAGTCGGT | 9873 |
rs142433632 | in-del | -/TATA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980676 | GTATGTGTGTGTGTG[-/TATA]TATATATATATATAT | 9873 |
rs142448157 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873599 | ATGATGTCTAATTTA[C/T]CTAGTTTTTCTTTTG | 9873 |
rs142464402 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124030 | GTCCATCAATGATAG[A/G]CTGGATTAAGAAAAT | 9873 |
rs142485523 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085096 | TAAGATCTTACTATA[C/G/T]TTGTTTTGAGTAAAT | 9873 |
rs142521777 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064237 | TGTTCTTTGAAACCA[A/T]TGAGAACAAAGACAC | 9873 |
rs142558696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131219 | AAATCCCATCTCTAT[A/G]AAAACTACAAAAATT | 9873 |
rs142558957 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979089 | TCTCAAACTCCTGAC[C/T]TCAGGTGATCTGCCC | 9873 |
rs142568333 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082730 | CATATTTTAAAATTT[G/T]TGCTACAAAGACAAC | 9873 |
rs142568897 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881146 | CAAGGGACTAATATA[A/C]GGAATATACACGGAA | 9873 |
rs142587978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981105 | GAGTTTTCCTGTACT[A/G]CAGACTATAGAATTA | 9873 |
rs142618697 | snp | A/C | 0.000148318 | 0.00861028 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72887556 | CAGCAGCTCCATGAC[A/C]CTCCAGATCATTTAG | 9873 |
rs142620764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024844 | AGGACATGAACAGAC[A/G]CTTTTCAAAAACAGA | 9873 |
rs142620849 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921261 | AAACATTTTAATCTA[A/T]CAAATCTTGAAGAAA | 9873 |
rs142624444 | snp | C/T | 0.000181376 | 0.0095213 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843194 | AACGAGTTCTGCTTC[C/T]GTGGAATTGCTGGAC | 9873 |
rs142629561 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989901 | GACTGGCAAAAGCTC[A/G]GCAAAGCAGGAGGAG | 9873 |
rs142637835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927449 | TGTGCCACTCTGATG[A/G]GGGATGTTGATAGTG | 9873 |
rs142660548 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864850 | ACAGGCTGATGGGGT[G/T]GCTGGCAGCAATCTA | 9873 |
rs142693354 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997470 | TCCAATATTGTGAGT[C/T]ATAATCAAACAGAAG | 9873 |
rs142695604 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094167 | AATGAGCCAAGACCA[C/T]GCCAATGCACTCCAG | 9873 |
rs142700060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002666 | GGAGATACCCTTCAT[C/T]CATGTTCTTCTCTCA | 9873 |
rs142702801 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939649 | TTTGAGACAGTGTCT[C/T]GCCCTGTCGCCCAGG | 9873 |
rs142724039 | snp | C/T | 0.000141794 | 0.00841883 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840843 | AATTTGGAAGAACTA[C/T]GCATTCGATAATCCT | 9873 |
rs142729788 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007387 | GCATTTTGGGAGGCT[A/G]AGGCAGAAGGATTGC | 9873 |
rs142730356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848513 | CTATAAATCTTTTCA[C/T]ACTTGTTCTATTTTC | 9873 |
rs142736469 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943054 | TGGAGTGCAATGGTG[C/T]GATCTTGGCTCACTA | 9873 |
rs142767971 | in-del | -/AA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851102 | CGTGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 9873 |
rs142861333 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059730 | TCTTTCTTTTTTTTT[C/T]TTTTTTTCCCCTAGC | 9873 |
rs142891668 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138096 | ATCAGCAATAATACA[A/C]ACTAAGCAACAGCAA | 9873 |
rs142899648 | snp | C/T | 0.000284542 | 0.0119243 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867911 | GGAGGGCGGGCCCAT[C/T]GCTCATTTTCCAGTT | 9873 |
rs142906284 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123533 | TGTAAAGTGCACAGG[C/T]GACTCTTGCTTTTAT | 9873 |
rs142916551 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854768 | GACAGAAAGCAGAAT[A/G]GTGATTGTCAGAGGC | 9873 |
rs142924895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934725 | TATAAATGTGAGTTA[A/G]TCTGGCAGTATGAAC | 9873 |
rs142927800 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837771 | AAATGTCAGGGTAGT[A/G]GGACCTGGAAGCTGC | 9873 |
rs142951785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108057 | GAGGGTCCCCTTTTC[A/T]CCACATCCTTGCCGG | 9873 |
rs142964299 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955042 | CAAGCAATTCCCTGG[A/C]AGATACCAGCTGGAC | 9873 |
rs142964390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054970 | ATACTTGAGACTGGG[C/T]AGTTTATAAAAAGAG | 9873 |
rs143009366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074188 | CAAAATATCACTTCA[A/G]TACAGTGCTGGAGTG | 9873 |
rs143029589 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903621 | ACATACCTTGGGAAA[C/G/T]AGTGGAAATCGGCAT | 9873 |
rs143031441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962259 | ACAAGTATGTGGTAT[A/G]GTTTTCTAGAGGCTG | 9873 |
rs143081503 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021504 | TAAATGGGAGCTAAA[C/T]GATGAGAACACATGA | 9873 |
rs143086970 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931271 | TTTTTTTTTTTTTTT[-/T]AGTAGAGATGAGGTT | 9873 |
rs143099261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960419 | TAGTCTGCTGCTCCT[C/T]TGGATTTAAATGGAT | 9873 |
rs143129014 | in-del | -/TTG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100335 | GCGCTTTACATGCTT[-/TTG]TTGTTGTTGTTGTTG | 9873 |
rs143131200 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906385 | TAGGGTGCCTGTTCA[C/T]TCTGATGATAGTTTC | 9873 |
rs143143356 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888134 | CAAGATAGCCAAGTA[C/T]AGGAATCTGAGAAAC | 9873 |
rs143180594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019545 | CAAAGCTAAACTGTA[C/T]TAAACTGAATGAGCC | 9873 |
rs143191185 | snp | C/T | 0.00769574 | 0.061552 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077705 | AATGAAATACTGATG[C/T]ACACAACAACATAAA | 9873 |
rs143215833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087513 | GAGTTTGAGACCAGT[C/G]TGCCAACATGGTGAA | 9873 |
rs143233093 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137424 | TAATTAAAGTGATCA[C/T]GTGAACCAAAGTATA | 9873 |
rs143233886 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922409 | GTGACAGAAAAAACA[C/T]AATAGAAATATTAAA | 9873 |
rs143247683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033612 | AAGCAACTACAAGCA[C/T]ATCCACACTCCCAAA | 9873 |
rs143255561 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007627 | AAGAAGAAAGAAAAA[-/AG]GGGGGAAAAAGAGAA | 9873 |
rs143283322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066254 | CAATGGGGAAAAGAT[G/T]ACCTATTTAATAAAT | 9873 |
rs143308827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874188 | CTAGCACCATTGTAG[C/T]ATGCTTTTGCTTTTT | 9873 |
rs143309417 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025732 | AATCTGTATACTTGT[A/G]ACTAAACTATATCTC | 9873 |
rs143353128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928544 | AACACAGGCAACTGA[C/T]ATTTACTAACGGCTT | 9873 |
rs143353518 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027710 | TCGCTGCACTCCCCG[C/T]CATCACAGGCCCAGG | 9873 |
rs143355152 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865213 | CCTCTAGAATGTGCA[C/T]TTCTGCTTCATGTTC | 9873 |
rs143382984 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117662 | GGGAATGGGAAGAAA[C/G]CTTCAACAGATTATT | 9873 |
rs143395790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103869 | CATGAACCAAGCAAA[C/T]TCTCCTCCAGAGAAG | 9873 |
rs143406067 | in-del | -/C | 0.0138799 | 0.0821421 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020679 | GTAAGATTAAAAAAA[-/C]AGTATATTATTTTAA | 9873 |
rs143407520 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969477 | AAAGATGAATCTTTG[A/T]CTTAATTTTTTGAGG | 9873 |
rs143408886 | snp | A/T | 1.64765e-05 | 0.00287019 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843514 | GTTCCTCAATGGTCA[A/T]CTCATCTGGTTGAGA | 9873 |
rs143410428 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867042 | AGAGAACCAGGAAGA[C/T]ATGGCAATTACATTC | 9873 |
rs143414149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011382 | GAACATGTGCACCAC[C/T]TAGGCTAGCAGGTGG | 9873 |
rs143430107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048497 | TAAATGCTAACTTCT[A/G]CTCATGAATCTGCAG | 9873 |
rs143430419 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991662 | CAACGACAAAAACCA[C/T]ATGATTATCTCAATA | 9873 |
rs143436453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73140990 | CAGACACGGGTGAGT[C/T]AGGCGTTAGGCAAAT | 9873 |
rs143461020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889736 | ACAAAACAACACATA[C/T]AGGATATTTTTCACA | 9873 |
rs143474930 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895536 | TCACAAGCTAGATAG[A/G]GGAACTTTCAGGCTC | 9873 |
rs143495237 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996612 | ATACAATTGTGTTTA[C/T]CTTCCAAGCATTATA | 9873 |
rs143501492 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140420 | CAAGCTCAATCCACG[G/T]CTAGGTCTTCCTACA | 9873 |
rs143514898 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911765 | TTTGTTGCCTAGGCT[A/G]GAGTGCACTGGCACA | 9873 |
rs143515808 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015688 | TTTTGAAATTATATC[C/T]GAAAACACAGCAGAG | 9873 |
rs143537137 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047680 | TGGGATTAGAACCCC[C/T]TTCTCTTTTCCTTTC | 9873 |
rs143543601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840467 | AATAATATATTCACC[C/T]GGAGAATAAACGCTC | 9873 |
rs143544414 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138381 | AAAATGGAGACAAAA[C/T]GCAATCAAGAAGTCT | 9873 |
rs143548146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855949 | AAAAACCTAATAAAG[A/G]AGAGACAAACAGCCT | 9873 |
rs143553457 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840119 | CCTATATCCTTTCTG[A/C]CACCCTCCATCCATC | 9873 |
rs143563717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937446 | TTCAGTAAACAATAT[C/T]TCTGATGCTGGCCAA | 9873 |
rs143606848 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994617 | AAAAATACAAAAAAA[C/T]TAGCTGGGTGTGGTG | 9873 |
rs143606909 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050666 | CCATATCCACATGGG[A/G]AGATAATGGGAACAT | 9873 |
rs143635163 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038445 | CAGATCAAGAAAAAT[A/G]GGCAGTGACTCAAGA | 9873 |
rs143652784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115514 | CAACTCTATACTTTC[A/G]TGTCGTTTTCATGTC | 9873 |
rs143654667 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009365 | AGCCAGGTGTGGTGG[-/C]CGTACACCTGTAATC | 9873 |
rs143658197 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847226 | TGGTCTCAAACTCCC[A/G]GCTTCAAGTGATCTT | 9873 |
rs143659152 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899521 | GAGGATCTTTTGAGC[C/T]CAGGAGTTCAAGGCC | 9873 |
rs143659400 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882482 | GATAAGTTCTGGTGT[G/T]TGATAGCTTAGCAGG | 9873 |
rs143659748 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844440 | AGACTGAGCTGATCC[A/G]TTTGCGTGCTACCGT | 9873 |
rs143663537 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982697 | AACTGTAATCTAATC[C/T]ATCTGCATTTCAGAG | 9873 |
rs143672859 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144258 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 9873 |
rs143701055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114943 | GGTGTCTCACTAGGT[C/T]ATGTGCCCCACCATG | 9873 |
rs143725899 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998837 | GATGTTGGCAAGGCT[A/G]TAGAGAAATTGGAGC | 9873 |
rs143760818 | snp | A/G | 0.000555104 | 0.0166506 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72921844 | TTGCTGGAGTTTTCT[A/G]ATAAAAACTGGAATG | 9873 |
rs143769564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118819 | CCATTTCTGTTTTAC[A/G]GATGAGAAAATTGAA | 9873 |
rs143776225 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904547 | CCACCCCTAATTATA[C/T]TGAAACAAGTTCCAG | 9873 |
rs143776544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975091 | TTCTGTTCCTGGCTT[A/C]TTTCACTTAACATAA | 9873 |
rs143787937 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115377 | TTTAGCAGAGATGGG[A/G]TTTCACTGTGTTAGC | 9873 |
rs143807686 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072247 | TTGGGGAGGAAAATA[A/C]TGGGGATCAGCATCA | 9873 |
rs143824289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022880 | GAGAGATCCCAGAAA[C/T]AGACCCATACAAATA | 9873 |
rs143837769 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917205 | GGCCAGGCTGGTCTT[C/G]AACTCCTGATCTCAT | 9873 |
rs143839705 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850124 | GCTGGACTGCAATGG[C/T]GTGATCTTGGCTCAC | 9873 |
rs143844192 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054741 | AGTGCAGTGGCACAA[C/T]CATGGCTCACTGCAG | 9873 |
rs143850216 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118387 | GTTTCCTCATGCCCC[A/G]TCTTAGTCAATTCCT | 9873 |
rs143851916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950821 | CTATTTGTTGTTGTC[C/T]GCCAAATGTTATCCC | 9873 |
rs143858039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090195 | AATGTTTACAAATAT[A/G]TATTTATGGTAATTA | 9873 |
rs143872333 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864107 | CATACTCTAAGTGAG[A/G]CTGTACAACAGAGTA | 9873 |
rs143899766 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970733 | ATGCGAATTCTTCTA[C/T]GAAGAAAAGACTTCC | 9873 |
rs143940649 | in-del | -/AG | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955621 | TTCAGGAGCCCACTA[-/AG]AGTTACTTCATTAAG | 9873 |
rs143942598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933536 | TTGGGTCATTGTTAT[C/T]TGCAATCAAAAGACT | 9873 |
rs143957676 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027033 | GGAAATGGAGTAATA[C/T]AGAAAATTGGTACCG | 9873 |
rs143959801 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116851 | CCATATCTCTTTTTT[C/T]AGTTATGAACTCAAA | 9873 |
rs143979928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879592 | ACCACATAGAACTTA[C/T]AGAGCTAAAAATATA | 9873 |
rs143999158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120008 | CAAGTCCCCTCTTAC[A/G]TGGATGGCAGAAGGC | 9873 |
rs143999802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969394 | ATTTAGGTTTTGCCA[C/T]CTCAGTTAATTTTTT | 9873 |
rs144001366 | in-del | -/C | 0.0235167 | 0.105855 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836507 | GTATTTCTTTTTTTT[-/C]CCCATGGGAAAAGCA | 9873 |
rs144027695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871538 | TCCACTTACTTAACC[G/T]AAGTAAAGTTCCACT | 9873 |
rs144064911 | in-del | -/A | 0.236724 | 0.249647 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099281 | AAAACAACACAAAAC[-/A]AAACAAAAACAGAAA | 9873 |
rs144136190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119508 | CTCACTCTGTCACCT[A/G]AACTGGAAGGCAGTG | 9873 |
rs144150140 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105665 | CATAAAGAACTCAAT[A/C]AATATTTATTATTAG | 9873 |
rs144157976 | in-del | -/AAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075426 | TCAGAAACAACAGAC[-/AAT]GACAGGTATTTGCTA | 9873 |
rs144182747 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097180 | GCTGATTTTTGTATT[C/T]TTTCGTAGAGATGGG | 9873 |
rs144183464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971294 | AGGAATAAATTTAAC[A/G]AAATACGTGAAGACT | 9873 |
rs144196683 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934146 | AAAAGAGCTATTTAA[A/G]GCTTACAACAAATCA | 9873 |
rs144200516 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842680 | AAAGTTCTTCCACTA[A/G]CACCGATGGGAAAAC | 9873 |
rs144205568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941109 | GTTCCACTGTTACCA[C/T]TAATATAAGTAAAGT | 9873 |
rs144291169 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143363 | CAGGAGAGGCCATAG[A/G]GGAAGCCCTTGTCTG | 9873 |
rs144311226 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016964 | AATGTATTATGTTTG[C/G/T]TTTTTTGCTTGTTTG | 9873 |
rs144320130 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998415 | GGTGTGGTGGCACAC[A/G]CCTGTAATCCCAGCC | 9873 |
rs144322316 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095972 | CTGTAAATTTGAAAG[A/C]CACAACCCTGAGCTA | 9873 |
rs144333124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047367 | GCATCTTATTCAAGG[C/T]TATAAGAAAAAAATA | 9873 |
rs144333577 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857883 | TGAGGTAGAAAGCAG[A/G]GTCTTGGGGTCTGGC | 9873 |
rs144344315 | snp | C/T | 0.000495878 | 0.0157383 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72902551 | CCCTTACAGTATCAC[C/T]GTCACAAGGCTGGAA | 9873 |
rs144381133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891995 | TTCCTAGGTTCTTAA[G/T]AGCCTAAACAATGAA | 9873 |
rs144393014 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951481 | GCACTTACTACAAGG[C/G/T]TTGGCATTTAGCTCA | 9873 |
rs144407351 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898046 | ATGAGACAGCTATTA[A/C]GTTACTACATAAGAA | 9873 |
rs144427542 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015069 | GGCTGGTCTTGAACT[C/T]CTGATCTCAGGTGAT | 9873 |
rs144435093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106050 | AACTGGGATGAACTT[C/T]AGAAATTATGTGGAG | 9873 |
rs144453070 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848538 | ATTTTCCAGTTTAAT[A/G]TTTAACCCTTCATAG | 9873 |
rs144457320 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131792 | GCTAAGAAAAAAATG[C/T]TGCCAATTAACACAA | 9873 |
rs144479618 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855554 | CTTAATGCCACTAAA[C/T]TTACACTTAAAGTGG | 9873 |
rs144488482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984381 | TTCATCACTACTAAG[C/G]AATGAAACAGTGACT | 9873 |
rs144510546 | in-del | -/T | 0.0629771 | 0.165899 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059720 | GTGAGGTTTTCTTTC[-/T]CTTTTTTTTTCTTTT | 9873 |
rs144520810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928566 | TAACGGCTTACTGAG[A/T]TCCAAGTGCTTTACA | 9873 |
rs144550444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109856 | AATGGCTTTTATTGT[A/G]TTGAGGTATGTTCCT | 9873 |
rs144552217 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953522 | ATCAATTTCAACCAC[A/T]TGAATTTATTGAACA | 9873 |
rs144561750 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016259 | AGTGAGCCGAGACTG[C/G]GCCTCAGCACTCCAG | 9873 |
rs144581326 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057880 | TGCCAATTCGGTATT[-/C]TTTTTTTTTTTTTTT | 9873 |
rs144605758 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856529 | AAAGGGAAAAGATTA[C/T]ACAGAATTGTGGAGA | 9873 |
rs144606913 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916004 | TCTCATTTGTAAGTG[A/G]GAGCTAAATTATGAG | 9873 |
rs144621421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057279 | TAGGACACAGTACAC[A/G]GGTTCGAAGCATGGG | 9873 |
rs144631789 | snp | A/G | 0.000370934 | 0.0136136 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72868025 | GCTTTCAATTTAATT[A/G]TCTAGAGAACCAAGA | 9873 |
rs144641029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861475 | AGACGAAATTCCATA[C/T]AATTCTACACAAGGC | 9873 |
rs144649889 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920967 | TACAAGAGGCATTCA[A/G]GATGAAGAGTCTGTG | 9873 |
rs144659156 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872281 | CACAACTTTTTTTTT[-/C]TTTTCTTTTTTTTTT | 9873 |
rs144749100 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135407 | AATAATTTTTCCATA[G/T]TATAGACCTCCTTAA | 9873 |
rs144756868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061276 | AGAACTCTGGAACAG[A/G]TACTGTGCTTGTCGC | 9873 |
rs144757924 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964325 | TGCACTGGCTCTTCC[C/G]TTTGCTTAAGATGTC | 9873 |
rs144765007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908912 | GCCCACCTTGGCCTC[C/G]TACAGTGCTGGGATT | 9873 |
rs144772331 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129226 | CAAATTACAGCTGGG[C/T]GCCATAATTTGTGAA | 9873 |
rs144772849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046759 | TTTGTTTATTGATTG[A/G]TTGATTAAGACAGGG | 9873 |
rs144784879 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133664 | AGCTGGGTACGGTGG[C/T]GGGCACCTATAATCC | 9873 |
rs144798246 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989940 | GAAGGACTATTGTGC[A/C]AGGGTGAATAGTGTG | 9873 |
rs144799677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137541 | ATAGCCAGTTACATT[C/T]GACAACAAGGGTATA | 9873 |
rs144832332 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993872 | TGTAACTAACCTGCA[C/T]GTTGTGCACATGTAC | 9873 |
rs144842254 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987380 | CACATTACTACTGCA[A/G]GTAAGTTATTAGTTA | 9873 |
rs144846314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085797 | CTGGTTCAAGTTGAT[A/G]TTTAAAAAAAAATGA | 9873 |
rs144867398 | in-del | -/TAACA | 0.0479149 | 0.147179 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106626 | GATAAATAAATACAG[-/TAACA]TAACATTTCCATAAA | 9873 |
rs144868637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088473 | CGTGTGTGTGTGTGC[A/G]TTTGTGTGTGTGTAC | 9873 |
rs144868987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866419 | GGATTATGGGCGTCT[A/G]CCACCATGCCTGGCT | 9873 |
rs144913712 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932732 | GTGATATTTGTTTGT[A/G]TGTCCCTCTTTTTGT | 9873 |
rs144917152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994953 | AACATTTTCCTACCC[C/T]AAAAAGAAACTCTGT | 9873 |
rs144933882 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092847 | CCCAAAGACAGGTCT[A/T]ACCTTTGTCTTTGGC | 9873 |
rs144939458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988672 | CATAGCAGTGACTTC[A/C]GGCTTTTGATAAGCT | 9873 |
rs144947548 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019095 | TCTGGTATTTTCTCA[A/G]ATCACATCTAAATGA | 9873 |
rs144952535 | snp | A/G | 0.000153988 | 0.00877327 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841544 | GGTCGTACAACGGCA[A/G]TGGAGGCAGGGAGGC | 9873 |
rs144955256 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993772 | GTGGGGTGAGGGGAG[C/G]GGGGAGGGATAGCAT | 9873 |
rs144955525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110677 | AATTTATTTCTGCTC[C/T]GATCTTTATTATTTC | 9873 |
rs144959029 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929785 | ACAAACTCCCCATCA[C/G]AGTATTTAAAACACT | 9873 |
rs144974943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860327 | AACAATAGCAAAATA[C/T]ACATTCTTTTTTTTA | 9873 |
rs144987216 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960011 | ACACATATTAATATA[A/G]GGTATTAATCTGTTC | 9873 |
rs144987798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892943 | ATATTAGCAGTGGTC[A/G]ATTCTAACAAAGAAA | 9873 |
rs144998272 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914982 | CTACAGAATGGGAAT[-/TT]TTTTTTTTTTTTTTT | 9873 |
rs145020567 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097943 | CCTCCAACTGGCTAG[C/G]ACTAGACTTGCATAG | 9873 |
rs145036173 | snp | C/G | 0.00239393 | 0.0345281 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839003 | GAAATGTTGTGAGCA[C/G]GTGCTTTCAACCTAG | 9873 |
rs145068964 | snp | C/T | 0.000444148 | 0.0148955 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72989037 | ATTTCTTTTTGCCTT[C/T]AGCTAAATCTTTCAC | 9873 |
rs145148955 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905726 | AGTTTGCTTAGAATA[C/T]TGGTTTCCAACTTCA | 9873 |
rs145150639 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060304 | ATCTTCATTTCTACC[C/T]ATTTATTATTATTAT | 9873 |
rs145182565 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065010 | TAACTCCTTTCATGA[A/G]GCCAGCATCATCCTG | 9873 |
rs145182795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106986 | CAGATATCCTGGACT[C/T]GACTTTTTAAAGCCC | 9873 |
rs145194022 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110624 | TCACAAAACCAACTT[C/T]TCATTTTGTTGGTCT | 9873 |
rs145197131 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961616 | TTGAGAAATGAATCT[A/G]AAGTGACTTGAAGAC | 9873 |
rs145240004 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959968 | TTTTAAAAGCACAGA[C/T]ATATAGGAAGAAACC | 9873 |
rs145240576 | in-del | -/TTGTTG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961406 | TTTTTAAGAAGTTTT[-/TTGTTG]TTGTTGTTGTTGTTG | 9873 |
rs145243066 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862365 | ATTTACAAAAAAGCT[A/G]CTAGAACTAATAAGT | 9873 |
rs145244617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087007 | TCCTACAGCTAACTG[C/T]AAAACAGCCTCAGGC | 9873 |
rs145245706 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988095 | TCTTGTGAATAAAAA[A/C]TGTATTAGAAAGATA | 9873 |
rs145253354 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866007 | CAAAGTTAGATGGTA[C/T]GTGCCTGCTCAGTTC | 9873 |
rs145279206 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966548 | TGCATAGCTTCACTG[C/G]AAGCTCCCTGCAAAG | 9873 |
rs145316351 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062933 | AATTCAGGAAATACA[C/T]AGAACACCACAAAGA | 9873 |
rs145337870 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859914 | AGTAAGGATACAGAA[C/T]AGCTGTCCCCAATCT | 9873 |
rs145346308 | in-del | -/TTTCTATTTT | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097672 | ACTTGTTATTGAGAA[-/TTTCTATTTT]TTTCTGTAATCAGTT | 9873 |
rs145360918 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842151 | GTGATGAACTAAGTC[G/T]AGGGTCACTTGAGTG | 9873 |
rs145393765 | in-del | -/AAGG | 0.281049 | 0.248064 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103219 | AAACTCTGTACACTT[-/AAGG]TAGATGGATTTTATT | 9873 |
rs145399490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940189 | CTTAGCCTTTTAAAC[G/T]CATCACTACTGAGAT | 9873 |
rs145405823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078994 | CAAGTGTTGGGATTA[C/T]AGGCGTGCGCTACCG | 9873 |
rs145412933 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027047 | ACAGAAAATTGGTAC[C/T]GAGAGACATGGCGTA | 9873 |
rs145457810 | in-del | -/ATA | 0.349452 | 0.229367 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039925 | TTAATATTCATGAGG[-/ATA]ATATCACAAAAGCAG | 9873 |
rs145484225 | in-del | -/GTTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016989 | TGTTTGTTTTCGTTC[-/GTTT]GTTTGTTTGAGACAA | 9873 |
rs145491476 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086829 | TGTCCCAGAAATGAA[C/T]AGATAAATACAATGT | 9873 |
rs145506517 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864130 | CAGAGTAGACTGGCA[-/G]GTTTGCCCTTGCACA | 9873 |
rs145516428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968276 | ATAAATAACACTGGT[A/G]CTCTGTCCTTAAGAC | 9873 |
rs145537418 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039166 | AGTCTAGTTCAAGAC[C/T]GTCTCACTGGGAGTA | 9873 |
rs145550076 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911279 | TTCTTGACAACTTTG[G/T]CAAAAATGAGTTCAC | 9873 |
rs145569785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036939 | ACGTTCATCTGTTAA[C/T]GCGGATCTGTAATTA | 9873 |
rs145578424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048209 | GCAGCAGGATATTTC[C/T]GTATATCCTGTTTAG | 9873 |
rs145586672 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139146 | TGAAACTAAAATCTT[C/T]GGGCTATAAACAGCA | 9873 |
rs145594238 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999311 | TTGAATCTTACCAAA[-/G]ATTCTTTTTTTTTTT | 9873 |
rs145603882 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042794 | TTAAATTTATTCCTA[A/G]GAATTTTACTTTTTT | 9873 |
rs145608151 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983017 | TAAAAGAAAGGGGCC[A/G]GGCGCGGTGGCTCAT | 9873 |
rs145608310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134198 | TCTCAGCACCATGCA[C/T]AGTGGCTCATGCCTG | 9873 |
rs145624750 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880510 | AAGGACACCCTCTTC[A/C]ATAAATGCTGCTGGG | 9873 |
rs145635734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839414 | AGGTAACAACTGGAG[A/G]AAGGATCAGAGGCAA | 9873 |
rs145687923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040134 | ATAATGTTACACAAA[A/G]GCTGAGTTCATTTGT | 9873 |
rs145694213 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953155 | CTAACAGTGCTGGAT[C/G/T]AGAAAGAAAAGGTAT | 9873 |
rs145694404 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050722 | TTTATATTGGTTGAA[C/T]GTTATGTCTCCATTC | 9873 |
rs145736647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73141056 | CACCCAGTGCCCAGA[A/G]TAGACATTCAGTATC | 9873 |
rs145750701 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935690 | AAATATCTTAATATG[C/T]AGTTGAATTTATCAG | 9873 |
rs145752852 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899623 | TCAGCTGTAGTCCCA[C/G]TTACTCGGGAAGCTG | 9873 |
rs145761048 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038002 | TCTGATGAAAAGATT[C/G]ACCAAGTCAAGCTTT | 9873 |
rs145788634 | in-del | -/A | 0.0482946 | 0.147699 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120031 | AGAAGGCAAAGAGGG[-/A]AATGAGGAAGATGCA | 9873 |
rs145823087 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890895 | TTGAGATAATTAGGA[A/G]TTTTTTTTAAAATAT | 9873 |
rs145851714 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053775 | ATGACAAAAAAGTTA[C/T]GACTATAGCAGCGAT | 9873 |
rs145860739 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031673 | TATTAACCAACACTG[C/T]TTATACCCAGGAATC | 9873 |
rs145880755 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837568 | ACAGTCAGCACCTGA[C/T]GTGGGGGCACCTGCT | 9873 |
rs145881197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016820 | GCCCACTTACTATTA[C/T]CTACACAACACAAAT | 9873 |
rs145885705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107397 | CAGGTGTATATATAG[A/T]TGAGGACATGAGATA | 9873 |
rs145886931 | snp | C/G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872743 | CTATTATGAATAATA[C/G/T]TGCTATAAACGTGTG | 9873 |
rs145901429 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902746 | ACAAATGAGAAATCA[C/T]CCAACACTGTGGTAA | 9873 |
rs145918758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020143 | ACTTTTAAAAAGCCA[G/T]CAGTGTCTGATGTTA | 9873 |
rs145919003 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954927 | CTGGCTGTATGTATA[C/T]GTAATAAAGATAGGA | 9873 |
rs145933818 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910386 | GTTTTGTCGAAAAGA[A/G]AAGGGGGAAATGTGG | 9873 |
rs145966742 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126016 | TGACATTAGGCAAGA[C/T]TCTATCTAATATGTT | 9873 |
rs145970097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077042 | ATGAACCCGGGAGGC[A/G]GAGCTTACAGTGAGA | 9873 |
rs145970411 | snp | A/T | 0.029116 | 0.117091 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131336 | TCCTGGCTAACACGG[A/T]GAAACCCCCTCTCTA | 9873 |
rs145971576 | in-del | -/AAATTAAA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024159 | ACTCTTAATATACGT[-/AAATTAAA]AAATTAAAAAAAATC | 9873 |
rs145974150 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956839 | GAAAAAAAAAAAAAA[A/C]CAACCCTAGAAGACA | 9873 |
rs145978076 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852752 | ATCAACCTAAATACT[A/G]ATCAATGACAAGTTG | 9873 |
rs145981476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979320 | AGAAGTCTCCCAAAA[A/C]GTACAACATAATGAC | 9873 |
rs145985107 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921552 | GTAGAATACAAAACT[A/G]TTTAAACCCTTCTCA | 9873 |
rs145985507 | snp | A/G | 0.000357782 | 0.0133702 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983849 | TAACAAATGTTTGCC[A/G]CACCTAGGGAATAAT | 9873 |
rs145989160 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082967 | GTAAAATTAAAGAAG[A/G]AAATGCTTCAATTTC | 9873 |
rs145997556 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948200 | TTTAGTAGAGATGGG[A/G]TTTTGCCATGTTGGC | 9873 |
rs146004687 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928100 | CTTTAAAATCATCAA[A/T]GCATTGGCCACATAT | 9873 |
rs146015778 | snp | G/T | 8.31663e-05 | 0.00644796 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840888 | TTACAGGTCGCAGTT[G/T]GCCATATGAGGTCTC | 9873 |
rs146033070 | in-del | -/TACTT | 0.0486741 | 0.148216 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098409 | TATGGGTAAAGAAAA[-/TACTT]TATATGATTTTGATC | 9873 |
rs146053285 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939638 | TTTTTTTTTTTTTTG[A/G]GACAGTGTCTCGCCC | 9873 |
rs146056703 | snp | A/G | 0.000489345 | 0.0156344 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867923 | CATCGCTCATTTTCC[A/G]GTTCTTCCATTACTT | 9873 |
rs146072965 | in-del | -/A | 0.0444908 | 0.142359 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950010 | TTTACATTCTCACCC[-/A]AATTTCTCCATCTCC | 9873 |
rs146092192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108356 | CCCATTCTGTGGGTT[A/C]TCTCTTCACTTTGTT | 9873 |
rs146092450 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050040 | GTTGCCAGGCCTCTC[G/T]ATATAAGAAGTCAGT | 9873 |
rs146103224 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951987 | TCTACATATTGTTGG[C/T]ATTTTCAACAGGCAC | 9873 |
rs146107435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955250 | GTTTGCTATAGTGGG[C/T]CACAGAACCCAAGGA | 9873 |
rs146111778 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055424 | TGGCAGAGCTGCCAC[G/T]TTCTACCCATACAGA | 9873 |
rs146161580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908292 | ATCTGTTGATGGACA[C/T]TTAGGTTGCTTCTAA | 9873 |
rs146171949 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096402 | AAAAAAAAAAAAAAA[-/TT]AGCCAGATGTGGTGG | 9873 |
rs146214858 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031059 | TCCTGCTATTTGTCA[C/T]AACATGTATGAATCT | 9873 |
rs146233135 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034782 | TTACTTATTAAGGAT[C/T]AGGTGAATTTTGACC | 9873 |
rs146233722 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125288 | TTTAAAGAAAACTAA[C/G]ATTATATTACGAGGT | 9873 |
rs146250321 | snp | C/T | 0.143622 | 0.226238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878881 | GGAGGCCGAGGCGGG[C/T]AGATCACTTGAGGTC | 9873 |
rs146313546 | snp | A/C | 0.00835141 | 0.0640778 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144402 | TGCCTGTAGTCCCAG[A/C]TACTCAGGAGGCTGA | 9873 |
rs146335642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099366 | GAGAACATAAAATTA[C/T]GTACCTGCTACAGAA | 9873 |
rs146345787 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005132 | TGGAGCATTCTTATG[A/G]GCAAACATGCTATAA | 9873 |
rs146349986 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013700 | ACAGTGTCTGCCACA[C/T]AGTAAATATTTTGTA | 9873 |
rs146356678 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104287 | TTATTTATTTATGGA[C/G]ACAGAGTCTCACTCT | 9873 |
rs146370009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951387 | AACATCTGGCATATG[A/C]TAACACAGCAAACGA | 9873 |
rs146371430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854432 | CTCTGTCTGTCTACC[A/T]ATCTGTCTATCTGGT | 9873 |
rs146404333 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857542 | CTCTTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 9873 |
rs146412375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969433 | TGTCTGAGAAAGAAA[C/G]AGAAAAACACTGAGA | 9873 |
rs146431182 | snp | A/T | 0.030278 | 0.119257 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064301 | AGTCTGTAGAGGGAA[A/T]TTTATAGCACTAAAT | 9873 |
rs146447439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911819 | TCTCTTGAATTCAAG[C/T]GATTCTCCTGTCTCA | 9873 |
rs146465744 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915610 | GATCACCTGAGGTCA[C/G]GAGTTCAAAACCAGC | 9873 |
rs146482717 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846181 | CTCCTCCTTTTGCTC[-/T]CTTTTTTTTTTTTTT | 9873 |
rs146501539 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134796 | CAAAAAATAAGAAAA[C/T]AAATTATTCCCTGAT | 9873 |
rs146519853 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047866 | GAGCTAATGACTTTG[C/T]TATCTCATTTAAGCT | 9873 |
rs146523967 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138382 | AAATGGAGACAAAAC[A/G]CAATCAAGAAGTCTT | 9873 |
rs146525743 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124175 | ACAGAAAACCAAACA[C/T]CGCATGTTCTCACTC | 9873 |
rs146539536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941271 | CACATAGAATGACAG[G/T]AAATATTTGTTAAAT | 9873 |
rs146555109 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042070 | TAGCTGGGATTACAG[A/G]TGCCCACCATCACAC | 9873 |
rs146556084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100267 | CAAGAAAACCCTTCT[C/T]CTATTAACAACAACA | 9873 |
rs146569969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946848 | GCCTAGGGAAATTTT[C/T]CAAGCTTAAGTAAAC | 9873 |
rs146573248 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886429 | TTCTGTGTTACACCC[A/G/T]CAACAATCCCTCCCA | 9873 |
rs146574639 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047520 | GAACAAAAAATACTG[C/G]TCATTGACAGTACCT | 9873 |
rs146588900 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892322 | GACAGGTAACTAATG[C/T]CACTGATTGGAAGAT | 9873 |
rs146618245 | snp | A/G | 3.29669e-05 | 0.00405984 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72984177 | AATCATTCCTTGCGT[A/G]GGTAGCTTTGGAATT | 9873 |
rs146621880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113875 | GGTCTTGGTTAAGAT[A/C]CAGAAGAATTCTCTA | 9873 |
rs146639431 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116903 | TTCCTCTTTATTCTT[C/T]GGTAAGAGTAATTAT | 9873 |
rs146655632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073588 | TATTTTTCTTTTAGG[A/G]TGGCTCACCTGTATG | 9873 |
rs146656054 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019722 | TCAGACATACTCTGG[C/G]GCTATTACAGTAAAG | 9873 |
rs146674345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078099 | GTACTCTTCTCTGTA[C/T]GTATATGTCAATTTT | 9873 |
rs146675050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981294 | CAATGCTGATCAAAT[A/G]TATGCATAAAGACTT | 9873 |
rs146684346 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079691 | ATCAAAAAGAGAGGA[C/T]AGAAATATCTTTGTC | 9873 |
rs146684896 | in-del | -/TTTTATATTCCCCACTCTATTTTATAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941442 | TAAATTATGTTGGAT[-/TTTTATATTCCCCACTCTATTTTATAT]GTCAGTTTGCTTAGT | 9873 |
rs146685430 | in-del | -/TATTTATA | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903200 | ATTTATTTATTTATT[-/TATTTATA]TATTTATTTATTTAT | 9873 |
rs146690834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922800 | TAAAATTCACCCAAT[A/G]TAAGTCACCATTTTA | 9873 |
rs146691231 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861892 | GCTGAGATCATGCCA[C/T]TGCACTCCAGCCTGG | 9873 |
rs146710424 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865486 | CAGAGGATATGTATG[C/T]CTCTAGAGGAGTGAT | 9873 |
rs146714169 | snp | A/G | 0.030278 | 0.119257 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870849 | AGCTTTCAGTGAGCC[A/G]AGATTGCGCCACTGC | 9873 |
rs146742719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093049 | GCTGGAGGCTAAGGC[A/C]AGCCGCATGAGTAGT | 9873 |
rs146749547 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917592 | TGTAGTTCCATATTA[A/G]TTCGAAGACTGGGCC | 9873 |
rs146778682 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994790 | AACAAAAAAAAGATA[A/T]AGTGCAAACTGTATC | 9873 |
rs146810894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998846 | AAGGCTGTAGAGAAA[C/T]TGGAGCCCTTGTGCA | 9873 |
rs146822591 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870922 | AAAAAAAAAAAAAAA[A/G]AATTCCCCCTTTGAC | 9873 |
rs146829948 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940761 | GCCTGTTCATCATGG[G/T]GTTAATCAGCTAAAG | 9873 |
rs146830265 | snp | C/T | 6.63196e-05 | 0.00575807 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843575 | ATTAAAAAGGTTAGA[C/T]AAGGAGCAGATGTGA | 9873 |
rs146834357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850263 | AGAGATGGGGTTTCA[C/G]CATGTTGGCCAGGCT | 9873 |
rs146865639 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113708 | TTCCAGGCATTTGAA[A/G]AAACACCCATTTGTA | 9873 |
rs146877390 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948684 | TTCTTTTTTTTTTTT[G/T]AGAGGCAGTCTCGCT | 9873 |
rs146880819 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071430 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 9873 |
rs146920683 | in-del | -/AAAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880068 | ACCAAAACAAGACAA[-/AAAC]AAAACAAACAAACAA | 9873 |
rs146921791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098718 | CAAGATTTCTACATA[C/T]AAAAAATGAAAGTGG | 9873 |
rs146951208 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102492 | AAGCAATGAAACGAA[A/C]CATCCATCAACTGAT | 9873 |
rs146963849 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125064 | AAAGTGAGGGTGAAA[A/T]AAAGACATTTTCAGA | 9873 |
rs146964933 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950033 | CCATCTCCTCACCAA[A/C]ACTTGTTATTTTCTG | 9873 |
rs146967520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048380 | TAGGCATTTCAGAGA[A/T]AATTCCTGCAAAACA | 9873 |
rs146973546 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052683 | GTGTGAATTGGACAA[C/T]TGGATTTATTCATCT | 9873 |
rs146981432 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894954 | TCTAAAATCTGGAAA[A/G]TTCTGAATTTTGACA | 9873 |
rs146981531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953872 | TCACATGTGAAAGTC[C/G]AGAGGTGACAATGTG | 9873 |
rs146992571 | in-del | -/TTTGT | 0.0267878 | 0.112589 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892601 | GTTTTTGTGTTTTTG[-/TTTGT]TTTGTTTTTTGTTTT | 9873 |
rs147027575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074361 | GCAAGTATAAAATAT[A/G]TGCAAGCATATGTGC | 9873 |
rs147056310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080717 | CGGAGGCTGAGGTGG[A/G]CGGATGATCTGAGGT | 9873 |
rs147068944 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925805 | GCCAGTGGCTACAGA[C/G]CCCTGCCCCTTCTGA | 9873 |
rs147072797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028993 | TCAGGTAGTTCTTCA[C/T]AGCAGTGTGAAAACG | 9873 |
rs147075849 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032604 | AAAAAAAAGCACAAC[A/G]AAGAGGAAAAACTCA | 9873 |
rs147085844 | snp | G/T | | | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867887 | AAAGTGCCATTACTG[G/T]TCACTGCAGGAGGGC | 9873 |
rs147088353 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873345 | AAAAAAAAAAAAAAT[G/T]AATCTTTTCATGTGC | 9873 |
rs147120594 | in-del | -/ACAG | 0.0279526 | 0.114869 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089278 | GCTATAATAAAACAG[-/ACAG]TAACAAGTATTGGTA | 9873 |
rs147129619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890169 | TCTTACACTGCTGAA[C/T]ACAAAAGCATCATCT | 9873 |
rs147130311 | in-del | -/AGATA | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846090 | GATAGATAGATAGAT[-/AGATA]AGTAGTTACGATTAC | 9873 |
rs147131855 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991678 | ATGATTATCTCAATA[G/T]ATGTAGAAAAGGCCT | 9873 |
rs147146693 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895701 | AAGCCTTTTGTGAAA[C/T]GCTGAAGAAATTAGG | 9873 |
rs147161252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997052 | AGAAAGAGGGGTACT[A/G]CAGAAAAGCAAGTCC | 9873 |
rs147216671 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063321 | AACAACCGGTACCAG[C/G]CACTGCAAAAACATG | 9873 |
rs147220007 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067652 | TAGGAGCTGAAAAGG[A/G]ACAAGTGCAAAATCA | 9873 |
rs147233902 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864334 | GGGAGGCCAACGTGG[A/G]CGGACTGCTTGATCC | 9873 |
rs147250096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971021 | TCACATTTGAGTTTC[C/T]CTAGCTGATGTGAGT | 9873 |
rs147280772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913983 | AGGAAAAATCAATAT[C/T]ATAAAAATGGCCATA | 9873 |
rs147320980 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040403 | TGTGAGATGTATAAA[C/G/T]ACATACACACAGATA | 9873 |
rs147325868 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132861 | CAGGTGATTCTTCCA[C/T]AGAATGGGAAAAAAA | 9873 |
rs147327239 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045831 | CTAGATGATGAGTTA[C/G]TGGGTGCAGCCACCA | 9873 |
rs147342795 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039511 | AACAGAGAGAGACTC[C/T]GTCTCCAAAAAAAAA | 9873 |
rs147356248 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884465 | AAATTTGGAAATAAT[A/G]TGATTAGAAATATAT | 9873 |
rs147356363 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943078 | CTCACTACAACCTCC[A/G]CCTCCCGGGTTCAAG | 9873 |
rs147372030 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044631 | ACAATAATAGAATTC[A/C]AACTCTGTCCTTAAG | 9873 |
rs147418267 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068813 | CATCTCTACAAAAAG[A/T]AAAAAAAAAAAAAAA | 9873 |
rs147426973 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017575 | AATTTGGTTTCACTA[C/T]TTCTAAGTATTGTGT | 9873 |
rs147430682 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110338 | CTTGGCTTTGCTAGG[C/T]GATATTTTATTACGG | 9873 |
rs147433238 | in-del | -/AG | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896179 | AGCATCTAGAATAAC[-/AG]GGAAAGATCATACAT | 9873 |
rs147433955 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115385 | AGATGGGGTTTCACT[A/G]TGTTAGCTAGGATAG | 9873 |
rs147443220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022889 | CAGAAATAGACCCAT[A/G]CAAATATAGTAAACT | 9873 |
rs147444597 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914129 | AAGTGATTCTCCTGC[C/G]TCAGCCTCCCGAGCA | 9873 |
rs147446351 | in-del | -/CTT | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100197 | TCAGAATCCCACCTC[-/CTT]GTCACCAAAATGTAC | 9873 |
rs147448318 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017169 | TTGTATTTTTAGTAG[A/G]CACAGTGTTTCGCCA | 9873 |
rs147460968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918581 | TCACAAAAAAGTACT[C/G]AATTTTGTCAAATCT | 9873 |
rs147477108 | in-del | -/C | 0.0287284 | 0.116357 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130871 | AGGTAATCTTTTTTT[-/C]CCCTCTCTTAAAGAA | 9873 |
rs147533718 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090734 | CTATTTGAATGTAAA[C/G]TATGTGCATATATAT | 9873 |
rs147536321 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094291 | TATAGCAATGAGGAT[A/G]AAGGGCAATGGAACT | 9873 |
rs147593241 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052904 | CAGACTGGAGAGCAG[G/T]GGTGTGGTGTCAGCT | 9873 |
rs147623099 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058713 | CAATTCTCCTGCCTC[A/G]GCCTCCCGAGTACCT | 9873 |
rs147638036 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906004 | TTCTAGATCCTTGAG[A/G]AGTTGCCACACTGCC | 9873 |
rs147642368 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014859 | CAAATTCTTTTTTTT[C/T]TTGAGCTGGAGTCTC | 9873 |
rs147653683 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852277 | CACTGCTGGTGGGAG[C/T]ATAAATTAGTTCAGC | 9873 |
rs147665190 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880868 | CGAAAAAAAAAAAAA[-/A]GAAAACAACAACAAC | 9873 |
rs147676031 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910069 | GCACCTCTGCCCGGC[A/C]GCCCCATCTGGGAGG | 9873 |
rs147695446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033005 | TTAAGAGTACTTAGA[C/T]TGGCCGGGTGCGGTG | 9873 |
rs147699293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123718 | CTTCAAAACATCACA[A/G]AGGCTGGAGAGTATA | 9873 |
rs147711868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036941 | GTTCATCTGTTAACG[C/T]GGATCTGTAATTAGA | 9873 |
rs147729004 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127772 | TTTAGGCACTTCACT[A/G]ATGCCTTCACCTGAG | 9873 |
rs147740269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980918 | CCAACAAATCAAATA[C/T]CCTGCTTTTAAGCTA | 9873 |
rs147740939 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880965 | ATGCTTCTGGACATT[C/G]GTCAAGGGAGATTTT | 9873 |
rs147756694 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986443 | CTCAATCTCCTGACC[G/T]TGTAATCCACCCGCC | 9873 |
rs147757013 | in-del | -/C | 0.0283406 | 0.115616 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102183 | TGAGATACCACTGAA[-/C]CACCCACTAGAATGA | 9873 |
rs147759110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880398 | TGGTATTGTCACAAA[C/T]ACAGACACACAGACC | 9873 |
rs147782509 | snp | A/C/T | 6.5893e-05 | 0.0057396 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842703 | GGGAAAACTCCAATA[A/C/T]GCCCATTGAATTCCC | 9873 |
rs147800570 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009312 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACTCCAT | 9873 |
rs147801880 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102004 | TGCAGACCCAGATAA[A/G]ATCCAATGCTACAAT | 9873 |
rs147816704 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015497 | TGTGTTTCATCATAG[A/G]TCACTCAGCAATTTG | 9873 |
rs147819361 | in-del | -/CTT | 0.0520825 | 0.152737 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865601 | ACAACGAGAACAGCC[-/CTT]CTTCTTTATCTCCTG | 9873 |
rs147831158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106370 | GTGATGGCACCACTA[C/T]ACTCCACCCTGGGTG | 9873 |
rs147844628 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953733 | TGAAGAAAAGATGCC[A/G]CCTTATGTTGTGTAG | 9873 |
rs147845987 | in-del | -/AAAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925544 | AACAAACAAACAAAC[-/AAAT]AAATTTCTAAACACT | 9873 |
rs147846068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855783 | GTGATATAGTGAATA[A/T]AAATAATATTTATAT | 9873 |
rs147861164 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959726 | GTTTACTGAAAGGAG[C/G]AATAGAAGTATTTAA | 9873 |
rs147862583 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860048 | TCATCAGGTATTAGA[G/T]TCTCATAAGGAGGGT | 9873 |
rs147866201 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855005 | TAGGCCAGGCACGGT[A/G]GCTCACACCTGTAAT | 9873 |
rs147891651 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130038 | GGCACCCGCCACCAC[A/G]CCCAGCTAATTTTTT | 9873 |
rs147907021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133680 | GGGCACCTATAATCC[A/C]AGCTACTCAGGAGGC | 9873 |
rs147920406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987460 | CCTTAAATTCCTTGA[A/G]GGCACAAAGCTTACC | 9873 |
rs147937273 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086237 | AACATGGCAAAACTC[C/T]GTCTCTACTAAAAAT | 9873 |
rs147950266 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930133 | ACTAAATCAATTGAG[A/C/G]GGCCAGGAGGAAAAA | 9873 |
rs147983751 | in-del | -/AT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931052 | TCATGTGCCTCACAA[-/AT]ATATATATATATATA | 9873 |
rs147997347 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140468 | CTTCTATTTCTAAAA[A/C]AGATTCAAAGACATT | 9873 |
rs148012524 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996560 | ATGTAATAATTCTCA[C/T]AATCCTCATTATAAA | 9873 |
rs148013752 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093374 | TGGTCTTGGGACCCA[C/T]AAAATTGCAAGTCGT | 9873 |
rs148017817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856088 | GGACAGGCAGGATTG[C/G]CCTTCATAGGAGAGC | 9873 |
rs148027442 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840358 | AAATTGCAAAGTATC[C/T]GACTGGATTACCGTG | 9873 |
rs148042453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937527 | ATGGACATATGGGAC[A/C]ATTAATGGAAAGGCA | 9873 |
rs148095650 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982897 | CAAGCACAATGGCTC[A/G]CACCTGTAATCCCAG | 9873 |
rs148097422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115210 | CTTCGACAGAACAGC[A/G]CTGAGTTCAATGGAG | 9873 |
rs148100572 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061438 | TACCCCAGTGGCACC[A/G]GGAATACCAGTGAGA | 9873 |
rs148115745 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113579 | TCGCCATGTTGCCAA[A/G]ACTTGGCCTTGATGC | 9873 |
rs148154083 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054879 | GAGGCAGAGGTGGGA[A/G]GACTGCTTGAGACCA | 9873 |
rs148161779 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917314 | GCATGTGGCTATCCA[A/G]CTGTCCCAAAACCTT | 9873 |
rs148167254 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903618 | TTTACATACCTTGGG[A/C]AAGAGTGGAAATCGG | 9873 |
rs148171052 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003055 | ACAATAAAAAGACAA[A/C]TCCTTTCATTAAAAA | 9873 |
rs148177966 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862594 | AAGTCCTAAATAAAT[A/G]GAGAAGTATATTATG | 9873 |
rs148197824 | in-del | -/AAAG | 0.0437281 | 0.141251 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125787 | AAAAAGAAAAAGAAA[-/AAAG]AAAGAAAGAAAATGG | 9873 |
rs148222210 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906857 | TGAAGTCAGGTAGCA[C/T]GATGTCTCCAGCTTT | 9873 |
rs148237286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888973 | TCTTTTTTCTTTTTA[C/T]TGAGACAGAGTCTCG | 9873 |
rs148240882 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135526 | ACAATCCTAAGAAGA[A/G]AAGTACACAGACTCT | 9873 |
rs148277938 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130166 | GGTGTGAGCCACCGC[A/G]CCTGGCCCATAATCT | 9873 |
rs148305589 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033997 | ATCATGAAAATATAA[C/T]AGACAATTTTAATAC | 9873 |
rs148313080 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017046 | GGAGTGCAGTGGCGC[A/G]ATCATGGCTCAATGC | 9873 |
rs148344441 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72849782 | AACAACTTTGCAGGT[A/G]AGTGGATAATTTCTT | 9873 |
rs148345193 | in-del | -/CCC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913822 | AAAAACCAAAAAAAA[-/CCC]AAAAAAAAAACAAAA | 9873 |
rs148366306 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104053 | ACAGCTCCCAAGTAC[C/T]TGAATGTCAGCCATC | 9873 |
rs148370809 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867449 | ACTAAGCCCACGTAC[G/T]AAGAAGAACATTCCT | 9873 |
rs148377994 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951000 | CTTCTCCATGCTCTC[C/T]TTCCCCTATCCACTG | 9873 |
rs148383061 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048642 | TAAGTGCCGGAAGTA[C/T]GAAAAAGCTGGAAAT | 9873 |
rs148393710 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848611 | CATCCCCCCAGTGTA[G/T]CACATATTGGGCACT | 9873 |
rs148398905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132229 | ACGATAACTTCCTTT[G/T]GTACCTTGAATAAGA | 9873 |
rs148410888 | snp | C/T | 8.47997e-05 | 0.00651096 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72985067 | GAAAACTTACCTTTA[C/T]ACTTGCCTTCTGTAA | 9873 |
rs148416020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085042 | AAATCATTTAAATTC[A/C]CCAAATGACTTGATT | 9873 |
rs148444805 | snp | C/T | 8.23934e-05 | 0.00641794 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72887547 | GTTCTGATACAGCAG[C/T]TCCATGACACTCCAG | 9873 |
rs148461912 | in-del | -/TTC | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110145 | TACTGGTCTGTAGTT[-/TTC]TTCTTTTTTTTTTTG | 9873 |
rs148468971 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023031 | TTGACACATACCTCA[C/G]GAGTTACACAAAAAT | 9873 |
rs148479323 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921185 | ATTTAATTTATCAGA[C/T]AAAAAACATTTGCCA | 9873 |
rs148482066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864517 | CACCACTGCACTCCA[A/G]CCTGGGCGATAGAGG | 9873 |
rs148501569 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050915 | AACAAAGGTCCTCCA[A/G]CTGTTTGTTACTGAT | 9873 |
rs148512536 | in-del | -/TTTTG | 0.499801 | 0.00998203 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866257 | CAACTCTGTTCTGTT[-/TTTTG]TTTTGTTTTGTTTTT | 9873 |
rs148531899 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964462 | TTCCTTCCCCTTTGT[A/G]CTACTACCACACTGT | 9873 |
rs148535285 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908942 | TACAGGTGTGAGCCA[C/T]TGCATGTTGCCCTGT | 9873 |
rs148554472 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047098 | GTGAATATAATTCTA[C/T]TTTTTTATAAAGGAA | 9873 |
rs148555291 | snp | C/G/T | 0.00319074 | 0.0398324 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137840 | TGCATGGGCATGAAA[C/G/T]GGTAGTAACTAAGCC | 9873 |
rs148569492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891922 | ATGTTAAAGACCCAA[C/T]TGAAAATTACTTGAA | 9873 |
rs148570856 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993961 | AGGCTTTGGGCTTCT[A/G]TGAGTACGGTGTATC | 9873 |
rs148622322 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036107 | CTAAAGGCTAAGAGT[A/T]GACTGGCTTGGACAG | 9873 |
rs148631389 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111305 | GCTCCAGTATTGGGT[A/G]CATATATATTTACAA | 9873 |
rs148634930 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879948 | AGCTTGACGTGAGCC[A/C/G]AGATCGCGCCATCGC | 9873 |
rs148649236 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124270 | TATTGTGGGATGGGG[G/T]GACGGGGAAGGGATA | 9873 |
rs148677276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119662 | CTGTGTTGCCCAGGT[G/T]GGTCTCACTCCTGGC | 9873 |
rs148679298 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971563 | TTGGTAATGGAGAAT[C/T]ATGTACAAAGGACCT | 9873 |
rs148681476 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105938 | TACCTATAGAAGATA[C/T]CTGGCAGAAGCAAGG | 9873 |
rs148694719 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953339 | CCTTTTTCACAATTT[A/C]TTTTTCAAAAAATCT | 9873 |
rs148700453 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983483 | TAAAAAATTAAAATT[-/A]AAAAAAGCTTCATAA | 9873 |
rs148712178 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007045 | TAAGTCCTTTGTACA[C/T]ATCATCTACTATTTT | 9873 |
rs148713592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100784 | CTATTGGGTAGCTGA[C/G]TCTAAATCTGGTGCT | 9873 |
rs148717235 | in-del | -/ATG | 0.498813 | 0.0243321 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958993 | ACTCATCAGTAAGAT[-/ATG]TGTGTGTGTGTGTGT | 9873 |
rs148746554 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857931 | TTGACTATGTCACTT[A/G]CTTGTTGTGTGACCT | 9873 |
rs148766705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096014 | TATCCTAAAGTGCTA[C/T]AGAAAAAAACAAAAA | 9873 |
rs148778084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940246 | CTAAATGGGGCTTTG[C/T]GTGTTTATATTATGC | 9873 |
rs148783664 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040965 | CCCACATATCAGTGA[A/G]TGAGAACATGTGATA | 9873 |
rs148794915 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885494 | ATAATAGGTCATCTG[A/G]CCTAAATGAAGACTC | 9873 |
rs148853768 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911537 | AATGGCACTGGTATT[C/T]TGAAAGAGACTGCAT | 9873 |
rs148870698 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015579 | TATATAAAATATAAT[C/T]TTGGCTTATATAAGA | 9873 |
rs148876541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139209 | AGTTAATATTTTTCA[C/T]GAAACCAACACGAAG | 9873 |
rs148884154 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855868 | TAGAGGAAATGACTG[A/C]CTTGCTTTTTATATA | 9873 |
rs148888549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995428 | AAAACTGGGCCAGGT[A/G]CGGTGGCTCACACCT | 9873 |
rs148930931 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130064 | TTTTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 9873 |
rs148936091 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899675 | CCAGGAGGTTGAGGC[A/G]CAGTGAGCCGTGATT | 9873 |
rs148947133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981996 | CAAAAACTATATATA[C/T]TAAAACACCTAAACC | 9873 |
rs148968336 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72902631 | TGAAGATTGTAGTCC[C/T]GGACCACCTAAAGAG | 9873 |
rs148983701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122626 | TTAATGAGGGAAAAA[C/G]AAGGGGACAGTTTAT | 9873 |
rs149000225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072076 | TGAGTGAAGACATAC[A/G]CAGACCACTATGTCC | 9873 |
rs149006588 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837760 | TCCTTCCACGGAAAT[A/G]TCAGGGTAGTGGGAC | 9873 |
rs149032628 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103619 | CTTTATGCCAACACA[C/T]AGTTCAATTAAACTA | 9873 |
rs149048029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019462 | TATCTATTTTTTTAA[A/G]TTATGAAATTAATTT | 9873 |
rs149064144 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960127 | CACAGTGCCAGGATC[G/T]ATTTCTGGTGAGGCT | 9873 |
rs149064589 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860366 | TGTAACAGTTACCAA[C/G]ATATACGTTTATACT | 9873 |
rs149082689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098367 | TTTCTGTCCCCTTCT[A/G]TTAATTGATTTCTAG | 9873 |
rs149086193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043915 | AACCTCAAGATTAAA[A/G]GAGCCTGGATCATTG | 9873 |
rs149095791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941924 | CATTAAAAAAGTTTA[C/T]AAAAGCATAAAAAAG | 9873 |
rs149135783 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134174 | AGTCTCTGAGACACT[G/T]AAAAAAAGTCTCAGC | 9873 |
rs149138489 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087293 | TTTATACAGTTGTAC[A/G]ATATGTGTTTTAAGC | 9873 |
rs149148129 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851519 | GCCGAGGTGGGCGGA[A/T]CACAAGGACAGGAGA | 9873 |
rs149150087 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947103 | GTCACTCTGGTTTAA[C/G]AGCTGCATGCCCCAT | 9873 |
rs149150936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988212 | AGTCAGCACACTGAC[C/T]CTGAGTCTCAGCTCT | 9873 |
rs149152120 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931086 | CCTACTATATACCCA[C/T]AATAATTAAATTTTT | 9873 |
rs149192643 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079689 | CAATCAAAAAGAGAG[A/G]ATAGAAATATCTTTG | 9873 |
rs149208066 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924268 | ATTTTGATGCAGTCT[A/C]ATTTAGCTATTTTTC | 9873 |
rs149209481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027694 | GGCATTTCAGAGATG[G/T]TCGCTGCACTCCCCG | 9873 |
rs149242627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053908 | TAACTTGTTGTCTGT[A/G]ATCTAAAAATTTTAA | 9873 |
rs149251166 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131662 | TAAGCCAAGATCGCA[C/T]CACTGCACTCCGGTC | 9873 |
rs149262603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983999 | CTGGCTACTCTTTTA[C/T]AGATTCAATCCCATA | 9873 |
rs149301323 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124870 | ATACTAGTCACATTA[C/T]ACTCAAACTGTAGGA | 9873 |
rs149310362 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894875 | AAAATACTATGTTTG[G/T]TCACAGGTGCTTCCC | 9873 |
rs149313870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839789 | GAAGAGATCGGATTG[G/T]CAGTTATAAATCTGA | 9873 |
rs149314558 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978664 | GTGACTGAGTTCTCA[C/T]GATATCTGATGGTTT | 9873 |
rs149331331 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075758 | GGGCAGAGTTTGCAG[C/T]GAGCCAAGATCATAC | 9873 |
rs149345507 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971183 | GAACAGGTCAAAATA[C/T]AAAAATCAATCATAT | 9873 |
rs149346859 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869967 | AAATATCTTTCACAG[A/T]TTGGCTGAGTTATTT | 9873 |
rs149408946 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046375 | ATGAATGGCCAATAC[A/T]GCAAGAATGCATTGT | 9873 |
rs149453288 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010308 | CTGAATTGTTTTTCT[A/G]ATTTCTCTGTACTGT | 9873 |
rs149462015 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090194 | AAATGTTTACAAATA[C/T]ATATTTATGGTAATT | 9873 |
rs149469294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853445 | TTGGAGACAGAGTCT[C/T]GCTCTGTTGCCCAGG | 9873 |
rs149474328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933398 | TGAAGATGGGAATGG[C/T]GGGCAGAGGACAGGG | 9873 |
rs149491382 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035234 | GTCTCGCTCTGTCAC[C/G]CAGGTTGGAGCGCAG | 9873 |
rs149523444 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887947 | TAAGTGGAACACTGA[A/C]TTTGAGACACCTGTG | 9873 |
rs149528333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030135 | AGTTATAAAACTGCT[A/G]CATGATAGCAGTACC | 9873 |
rs149556223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920831 | ATAGGAAAACAGATA[C/T]ATGACAGGACTTCAA | 9873 |
rs149596681 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066036 | AACCAAAAAAGAGCC[C/T]GCATTGCCAAAACAA | 9873 |
rs149602034 | snp | A/G | 0.021333 | 0.101051 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73142938 | GGGCGCAGCATGCCT[A/G]TGGGATACGAGAATT | 9873 |
rs149611292 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913614 | TTTATTGGCATATAT[G/T]GTTCACAGTAGCCTC | 9873 |
rs149612773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016926 | GTTAAGAATTGATTT[C/T]AAACTGCTCATTCCA | 9873 |
rs149618147 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095814 | CAAACAAGCCACGCT[A/G]GCAGAAACTGAGTTG | 9873 |
rs149626850 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857827 | ATCTTCTTGTACTCA[C/T]TAAAAACACCTCTGA | 9873 |
rs149664177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973622 | GGAGATGTTTTGGGA[A/G]GGGTCACCTGGGAGA | 9873 |
rs149685109 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884312 | TTGAATCTAGATGTT[A/G]GGAAATACATGTTTA | 9873 |
rs149704195 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115992 | ATCACAGGGGCACAA[A/C]TGTGTTATCCACGAG | 9873 |
rs149707276 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063694 | GAAAGAGACAAAGAA[C/T]GGTATTACATATTGG | 9873 |
rs149708497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101974 | AGTCCAAAATCTGCA[A/G]GGTAGGCCAGAAGCT | 9873 |
rs149758898 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104929 | TTACAATATAGTTTT[A/T]CACGTTTAAATGAAT | 9873 |
rs149771427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014509 | TCAAGACACCTTCCA[C/T]GATATCAGTAGGCCA | 9873 |
rs149772506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952323 | GTGTTCACCAAGTTT[A/G]ACTATCTTTTTTTTT | 9873 |
rs149806975 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037463 | ATCCTCAACTTCTGG[C/T]AACTACTGATCTTTT | 9873 |
rs149828222 | snp | C/T | 0.281841 | 0.247964 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944315 | ATATGATTATCTCAA[C/T]AGATGCAGAAAAGGC | 9873 |
rs149843295 | snp | G/T | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72902587 | AGGGCTGGGGTTTGT[G/T]AAATACAGCGTTTTC | 9873 |
rs149845018 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890668 | TGGAAAGTGCTTCAT[A/G]TAACTTTTTTTTTTT | 9873 |
rs149856886 | in-del | -/TTGTTGTTG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961406 | TTTTTAAGAAGTTTT[-/TTGTTGTTG]TTGTTGTTGTTGTTG | 9873 |
rs149860774 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031657 | GACCAACAAAGGACC[A/C]TATTAACCAACACTG | 9873 |
rs149862249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121133 | AAAAGCAATTAAGCA[C/T]ACCCTTTGGGGTCTC | 9873 |
rs149878215 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924084 | TTTCACTTTCTTGAA[A/G]GTTTCTTTTGATGTA | 9873 |
rs149924832 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879500 | ACAAGAACTTTAAAA[C/T]TGCTGTTATAAATAT | 9873 |
rs149929919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019027 | GCAACATATGGGTTA[C/T]TGCCAAACAAGTGGC | 9873 |
rs149932797 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860148 | GCTGGTCTGACAGGA[C/T]GCAGAGCTCAAGCAG | 9873 |
rs149982029 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057032 | AGCTTGCAGTGAGCC[A/G]AGATCACACCACTGC | 9873 |
rs149985061 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005678 | ATAAGGTCTTGCTCT[G/T]CCACTCAGGTGGTAG | 9873 |
rs149989276 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041776 | TCAATTTTGTGTTTT[C/G]GTTTGTTCACAGTTT | 9873 |
rs149992039 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059279 | TTTACCCTCCGTGGG[-/T]TTTTTTTTTTAACCC | 9873 |
rs149998754 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077130 | AAAAAGAAAAAAAAG[-/A]AAAAAAAAAGTTTGT | 9873 |
rs150002719 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851080 | GCACTACAGCTGGGG[C/T]GACACAGCGTGACTC | 9873 |
rs150003161 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134064 | AGTCACATCATGTAA[C/T]TTACATGATATGTAC | 9873 |
rs150038311 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998065 | TGTTAAATATTCAGA[C/T]TGAAGTACACAGAGA | 9873 |
rs150052638 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940046 | GTGTTACAGCCTGTA[C/T]AGAAAATGCAAGCAA | 9873 |
rs150056236 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127681 | CAAGAGTAAATTGCC[A/T]ATCATCAATTATTAA | 9873 |
rs150073025 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078916 | ATAGAGATGGGGCCT[C/T]ATTATGTTGTCAGGC | 9873 |
rs150078842 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107249 | TAGTAGAGACAGGGT[C/T]TCACCATGTTGGCCA | 9873 |
rs150087439 | in-del | -/AAAC | 0.244643 | 0.249943 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868691 | GCAAGACTCTGTTAA[-/AAAC]AAACAAACAAACAAA | 9873 |
rs150094087 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954362 | CACAGGTGCATGCCA[C/T]CATGCCTGGCTAATT | 9873 |
rs150145659 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048138 | ACTTGACAATGTTAG[C/T]ATATCAAACTGCAAA | 9873 |
rs150148356 | in-del | -/CCCCC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123137 | TTTATAAACAAGCCA[-/CCCCC]AACCGCCACTCTCTT | 9873 |
rs150168360 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124640 | GTGTGCCTCTAATCC[C/G]AGCTACTCAGGAGGC | 9873 |
rs150169582 | in-del | -/T | 0.031825 | 0.122064 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971372 | TATAATCCCCTTTCC[-/T]TTTGAGTGTCAGTAG | 9873 |
rs150180023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034490 | ACTAATGTTAAAATT[C/T]GGTACCAGAGGCTGA | 9873 |
rs150181977 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029773 | TTGAAAATTAGGACA[C/T]TGAAGGGCAATTGCA | 9873 |
rs150228321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935476 | TAAATATCAAGATGA[C/T]GATAAATGTGAGTTG | 9873 |
rs150235624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114012 | GGGCCTCTGTCCTTC[C/G]CTTTAGGGTGGCAAT | 9873 |
rs150246305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863062 | TGAGTAGCTAGGACC[A/G]CAGGAATGTACCACA | 9873 |
rs150249064 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962501 | TGATATTCACTGTAA[A/G]AAGAACAGGAGTTTA | 9873 |
rs150286279 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059903 | ATTTGTTGTACCAAA[A/G]CTTTGCTTATATCTG | 9873 |
rs150302160 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907036 | CCATTTGTTTGCGTC[C/T]TCTTTTATTTCGTTG | 9873 |
rs150321791 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136386 | GTAACATGGTAAGAC[A/C]CCATGTCTACAAAAA | 9873 |
rs150332516 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853209 | ATACATGATTAAATG[A/G]TTTTCAACAAGGATG | 9873 |
rs150363993 | snp | A/G | 0.000219452 | 0.0104727 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73015858 | GCCAATCTCTCTTCA[A/G]GTATTGACTAGCCAA | 9873 |
rs150368027 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846203 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACAGTGT | 9873 |
rs150370971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097925 | GCGATCCTCCTGCCT[C/T]GGCCTCCAACTGGCT | 9873 |
rs150383005 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941821 | AATCTTTGTTTTTGA[C/T]CAGGGAATGTAGCTT | 9873 |
rs150417770 | snp | A/G | 2.01177e-05 | 0.0031715 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867872 | AATCGTACCGAGTGT[A/G]AAGTGCCATTACTGG | 9873 |
rs150420652 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886384 | ACTAATCAAATACTA[C/T]TCATCTGCCAGCATT | 9873 |
rs150430378 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118244 | AAATTGCTTGGACTC[A/G]GCAGGCAGAGACTGC | 9873 |
rs150436386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987958 | TACAATAAAACAAAT[C/T]AGAGAAATATTAAAT | 9873 |
rs150445293 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970613 | CCACTGGTTTCTTCT[C/G]TGCATTACTTTCACT | 9873 |
rs150447374 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065626 | TCGTCTCAGTCCAAA[A/G]TCTCCTTAAGCTGAT | 9873 |
rs150462084 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913257 | TAGGTTGCATGCATC[C/T]AGGAATTTATCCATT | 9873 |
rs150536129 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066614 | AGGGCTAATATCCAG[A/G]ATCTACAAAGAACTT | 9873 |
rs150552509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025527 | AGATAATGAGAAAAA[A/G]ATAACTAATGGGTAC | 9873 |
rs150604096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927172 | AAGATCCTTCAGATA[C/T]GAGCTGCCTTCCATT | 9873 |
rs150608202 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062756 | AAAGAATAAAAAGGA[C/T]GAACAAAGCTTCCAA | 9873 |
rs150620198 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869157 | GGTGATCCACCTGCT[G/T]CAGCCTCCCAAAGTG | 9873 |
rs150637500 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014217 | GCTCACTGCAGCCTT[C/G]AACTCCTGGGCTCAA | 9873 |
rs150690788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098980 | ACACTTTGGGAGACT[A/G]AAGCAGGAGGATCAC | 9873 |
rs150699430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849205 | AAGAGAAGATTCATG[C/T]ATTCACGCCTCCCTT | 9873 |
rs150705258 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944085 | ACCAAAGCCTGGCAG[A/T]GACACAACAAAAAAA | 9873 |
rs150747224 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119845 | TACCATAAATATACA[A/C]GGATGTAAATAAGAA | 9873 |
rs150761733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933075 | ATAAAATATATATAA[A/C]CTTGCATGCCTTCTT | 9873 |
rs150763783 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972307 | TTACCTCAAAAAACT[A/C]TAAAATTAAGATCAT | 9873 |
rs150763977 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068952 | TAAAGAAGGTCGAGG[C/T]TGCAGTGAGTCATGA | 9873 |
rs150767189 | snp | C/T | 0.000206872 | 0.0101683 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841499 | GGGAGCTCCTCTTAT[C/T]TGGGCTGGGGTAGGG | 9873 |
rs150817025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109402 | CTTCAATTTCTTTCA[C/T]CAATGTTTTATAGTT | 9873 |
rs150822952 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875566 | ACTCCTGGCCTCAAA[C/T]GATCCTTCCGCCCTC | 9873 |
rs150846197 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055850 | CAGAAAGTAGATTCA[A/G]GGGCTGTGGGAGGAG | 9873 |
rs150863314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905088 | GTTCATGTCCTAATT[C/T]CCAAAACCTGTGAAT | 9873 |
rs150900658 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049319 | CTCATACCCACAACA[A/C]TATTAAATTTGGTTC | 9873 |
rs150901635 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142057 | CGGACCCCAGCCAGA[A/G]AGCGAGTGTGAGGAG | 9873 |
rs150912808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896813 | ATATGCTTGCCTTGT[A/G]GATTTTTGTTTTGTT | 9873 |
rs150917575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997515 | AAATCAAGAAAAACC[G/T]CAGGCGGTTAAAAGA | 9873 |
rs150935795 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871881 | ACAGGTGTGAACTGC[G/T]GTGCCCAACAGGTAC | 9873 |
rs150945500 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107046 | AAAGCTATATATATA[C/T]ATATATTTTTAAATG | 9873 |
rs150954696 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015748 | TGTTACATTATCTAT[A/G]TGTAACATAGCTTTA | 9873 |
rs150967585 | in-del | -/C | 0.0410537 | 0.137264 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916466 | AACAGGTATGCAGCA[-/C]CATGTCTGGCTAATT | 9873 |
rs150989206 | in-del | -/AAAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864608 | TGTTTGTCAATTAAA[-/AAAT]AAATAAATAAGAGTA | 9873 |
rs151008705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101211 | ATAAAAAGGCCACAT[A/G]AAATAGCAGATAAAT | 9873 |
rs151062289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138127 | CAGGAGCAACAGACT[A/G]TATCAACTTAGCTTA | 9873 |
rs151064107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994303 | CTTCTAAAAAGACCC[C/T]TTGTGGGCACTGCAC | 9873 |
rs151065029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091277 | GGCATGGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 9873 |
rs151076964 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838634 | CGAAATATTCAAAAC[A/G]TGGGAGGAGTCTACC | 9873 |
rs151082202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934972 | CACGTCCTTTCCAGG[C/T]AGCTATTAGGCCACA | 9873 |
rs151099675 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073164 | TTTTACCAACACCTC[A/C]GTGGTTAGCTAATTG | 9873 |
rs151135971 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980015 | CAGGAGGGGATGAGA[A/T]ATAATCCAAAGCTGA | 9873 |
rs151152781 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112776 | GCCTCAGCCTCCTGA[A/G]TAGCTGGGGTTACAG | 9873 |
rs151167846 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960751 | TGTGGAGAAAGGGTA[C/T]GGGGCAAGGGACAGG | 9873 |
rs151168876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059610 | ATGGTAAGAGGAAAA[A/G]CAAAATTAGTCTATG | 9873 |
rs151217357 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914691 | GCCATATGCAGAAAA[C/T]TGAAACTGGACCCCT | 9873 |
rs151232993 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901105 | TTTAAACAATTGCCA[A/G]TTGGGGCCGGACATC | 9873 |
rs151239951 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893473 | GCATATGCCATCACA[C/T]GCAGATAATTTTTTT | 9873 |
rs151277201 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041249 | GATAAATATCCAGTA[A/G]TGAGATTGCTGGATC | 9873 |
rs151288942 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885763 | CCAGTGTTTCTTAGA[G/T]TAGATGAGGGCTTGC | 9873 |
rs151307612 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028531 | ACTTCCTTGTCTCAG[A/G]TGAGACTTTGGCCTT | 9873 |
rs151308853 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117697 | AATTTTTCAATCACA[C/T]TGTAAAGAATTTTAC | 9873 |
rs151320549 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049873 | GCACAAAAGGACCAT[-/A]AAAAAAAAATTGTTT | 9873 |
rs180682661 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850326 | CACTTCGGCTTCCCA[A/G]AGTGCTGGTATTACA | 9873 |
rs180775596 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974183 | TGGTTCATGGTTCTC[A/G]GGACTGGGAAGTCCA | 9873 |
rs180797947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932434 | TACAGACCACATTAT[C/T]TGAACTTGGCATACC | 9873 |
rs180798153 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031411 | AGGGCGGGAGGTGGA[A/G]GCTGCATTGAGTTGT | 9873 |
rs180803981 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012926 | TTCCCTACAACTTGA[C/T]TTCTGCTACAATTTC | 9873 |
rs180805587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952300 | TCCATACACTTTTTT[A/G]TTTGCTTGTGTTCAC | 9873 |
rs180805990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995109 | TCTCACTTCTTTCAC[C/T]TATCAAAACATTTTT | 9873 |
rs180816339 | snp | A/T | 0.0501905 | 0.150254 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878000 | ACTGTCTCAAAAAAA[A/T]TTTTTTTAAATATAT | 9873 |
rs180826664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869325 | ACAACAATCTTGATA[A/T]TCACTAGCAATTCTT | 9873 |
rs180829310 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914512 | AGGGCCACAGCAACC[A/C]AACAGCATGGTACTA | 9873 |
rs180829720 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885285 | AAATGCTACAGATAT[A/T]CAAAACTGAGAAAAC | 9873 |
rs180837744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840817 | CGGGGAAACATTAAT[C/T]CCTTACTTTCAATTT | 9873 |
rs180859719 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139801 | ACTAGTAAGACTTTT[A/T]AGGTCCTTGTTTTTT | 9873 |
rs180859870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121885 | CATTTTTAACAAGTT[C/T]CAGATGGTGTTGATA | 9873 |
rs180862222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895748 | CTTAACTGTCAGTAT[G/T]GCTAATTCTAAAACG | 9873 |
rs180881361 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836799 | TAAATACAAACTTTT[C/T]ACAGCCACTGTAAAG | 9873 |
rs180887054 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860810 | GTGACAGAGCAAGAC[C/T]CTGTTTGAAAAAAAA | 9873 |
rs180914478 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023608 | AATAGTATGGCCACT[C/T]TGAAAGACAGTTTTG | 9873 |
rs180916909 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079618 | CTATAGAAAGAATAT[A/G]CTAATTATTTCAGAG | 9873 |
rs180923953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099454 | ACCCCAAGGTATATA[A/C]TCGAGAGAAAACAAA | 9873 |
rs180937592 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051915 | CACACACACACACAC[A/C]CCCCACACACACTGA | 9873 |
rs180947828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131158 | AGCTTGAGGCAGGCA[A/G]ATCACTTGAGACCAG | 9873 |
rs180955809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086198 | TGGATCACTTGAGGC[C/T]AGGAGTTTAAGACAG | 9873 |
rs180956528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067839 | TGAGGTACCTGCATT[A/C]GTCCATTTTCACACT | 9873 |
rs180959279 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041480 | ATTTCCCTGATGATT[A/G]GTGATGCTGAGCATT | 9873 |
rs180968003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060075 | AGGATACACTGCTAT[C/G]AGAGATGACTAACAC | 9873 |
rs180977770 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006019 | CTCAAGTGGTCCTCC[C/T]GCCTCAGCCTCCCAA | 9873 |
rs180978966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875265 | AAAAAAGCTCCAAAC[A/G]GCTTTTATCATAGGT | 9873 |
rs180982227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854773 | AAAGCAGAATGGTGA[C/T]TGTCAGAGGCTGCAT | 9873 |
rs180984692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903136 | TTCTTGAGGAGGTTA[C/T]ACTCTAATTACCATC | 9873 |
rs180987795 | snp | C/G | 3.34286e-05 | 0.00408818 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849719 | ATCTTCAGAGTTAAT[C/G]AGAATTTAATAACAT | 9873 |
rs180997092 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108762 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCTTGTT | 9873 |
rs181009649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881046 | AGGACTACATTAAAT[C/T]AAAAACTCTATGCAG | 9873 |
rs181018773 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990108 | ATGGACAGATAAAAG[A/C]AAAATAACCACTCAT | 9873 |
rs181019062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864993 | TTACATTCTGTACTA[C/T]AGCATGATACAGAAG | 9873 |
rs181021437 | snp | A/G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926936 | AGTGAAAAAAATGGC[A/G/T]ACTTGGTGCACTAGT | 9873 |
rs181030563 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962602 | GAACTAAATTCCCCC[C/T]TTTTTTTTTAAACTA | 9873 |
rs181035671 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845862 | CTTTGAACCTCAGTT[G/T]TCTTTTTTCGTACTA | 9873 |
rs181064660 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864132 | AGAGTAGACTGGCAG[G/T]TTGCCCTTGCACATT | 9873 |
rs181082910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013508 | ACCGCTGACATGTAG[C/T]AGGTATTTCATATGT | 9873 |
rs181083352 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006085 | GCTATTTTTTTTTTT[A/T]AATAAAAATAGTATC | 9873 |
rs181089609 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907409 | GCATCCTTATCTTGT[A/G]CTGGTTTTCAAAGGG | 9873 |
rs181090307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004674 | CTACCTTGGTTAAAT[A/C]TAAAACTGTTTACAT | 9873 |
rs181091131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040804 | ATCCGACTGTGCTAT[A/T]AAATACTAAAACGTA | 9873 |
rs181092521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921616 | AAGCTACCTTGTATC[A/G]GCACCTCTCTTTTTG | 9873 |
rs181092522 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985290 | TTTATTTTACTACAG[C/G]AAGAATTTATTATCA | 9873 |
rs181097056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058752 | TTTGAATTTTTAGTC[A/G]AGATGGGGTTTTACC | 9873 |
rs181097667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941213 | TCCTTCAAGGGACCA[A/G]AGGCCACATGAGTCT | 9873 |
rs181099149 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964166 | GAAATGATGTAACAG[A/C]AATCAAGAGAATTAC | 9873 |
rs181104804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996009 | AAAAAATAATAAACA[C/T]AAAGGTTATGTAGAA | 9873 |
rs181110602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022554 | GGATCTGTATGTGGA[A/G]AAGTCCATAATACTA | 9873 |
rs181111662 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052415 | GTATAATTTTTTTTT[A/T]AAAAAAAGACACCTG | 9873 |
rs181112298 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098611 | TAGTCCAGGAAAAAA[A/C]AAACAAACATCTATG | 9873 |
rs181112902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974698 | ACAAGTACCAGTGGT[A/G]AAGGCACAAATATGA | 9873 |
rs181116107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068626 | TAACAAAATTAACAA[C/T]TGGAACACACATTTG | 9873 |
rs181125043 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031997 | CAAGAGGAACTATTA[A/T]CTAAATTATGGTCAT | 9873 |
rs181128661 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120685 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 9873 |
rs181136214 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077726 | ACAACATAAACTACA[A/G]AATAGTTAATGCTAA | 9873 |
rs181141546 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914836 | TGGGCAAAGATTTCA[C/T]GATGAAGATGCCAAA | 9873 |
rs181152218 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933337 | TGTAGTAGGAAAGAA[C/T]TAAACCAACTCACAG | 9873 |
rs181178523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896226 | AGCTTTTTGCTGTCA[C/T]GATCTGTGAAGATCT | 9873 |
rs181185749 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085827 | AGAGCAGAGTTACCA[C/T]ATTATTACATTCAAA | 9873 |
rs181214814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110111 | TGTGGAGGATTTTTG[C/T]ATCAGTATTCATCAG | 9873 |
rs181228674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881688 | ACACACAATGGAATA[C/T]TATTCAGTCATAAAA | 9873 |
rs181230154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865618 | TCTTCTTTATCTCCT[A/G]TTAAAATTCTTCAAA | 9873 |
rs181248924 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086454 | CAATCTCAAATCAAC[A/T]GCCTAACTTTACAAC | 9873 |
rs181251366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846616 | TTACCCCAACTAAAG[A/G]CAGTGAGCAGTAAAT | 9873 |
rs181263952 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138421 | ACAACCAACAGAAAT[C/T]ATTACAACTACTGAC | 9873 |
rs181265370 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903629 | TGGGAAAGAGTGGAA[A/G]TCGGCATCTGATGGG | 9873 |
rs181282423 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917087 | CCTTTCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 9873 |
rs181296282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956579 | AGATCAAGGCGCCAG[A/C]AGATTTGGTGTCTGG | 9873 |
rs181359503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115896 | AACATCCACAAAATG[A/C]CTTCATGGCAACATG | 9873 |
rs181363447 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064838 | TGAATAAACCAATAA[C/G]AAGTTCTGAAATTGA | 9873 |
rs181367368 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046654 | ATATAGATAGACTTC[A/G]CTTACAAGGAAGCCA | 9873 |
rs181380863 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936750 | TTGTATTTTTAACTC[A/C]AGAATTTATATTTGA | 9873 |
rs181395072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969184 | AGCCATGTCAAAATC[A/C]GTGTTAACAGTCTAC | 9873 |
rs181414633 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904081 | AGTGTGTAAAGGGTA[C/T]GAGAAGAGAACAAGG | 9873 |
rs181421003 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055241 | TGGGGATTATGGGAG[C/T]TACAATTCAAGATGA | 9873 |
rs181421111 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028206 | GGCACTCAATGGCAG[C/G]CTGTGAAAGTAGCTG | 9873 |
rs181422098 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104524 | ATCCAGCCTCCCAAA[A/G]TGTTGGGATTACAGG | 9873 |
rs181424075 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072012 | TTTTTTGATCAGCGG[C/T]CAGGGCAGGGGACTC | 9873 |
rs181424154 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010047 | TAATATGTGTATTTG[G/T]TCACTTTATGTTGTC | 9873 |
rs181426916 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947976 | ATAATTTTTATGACA[C/T]CGTTTGGGTATCATA | 9873 |
rs181427267 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034709 | TTCAACTTCAATAAA[C/T]TTATTTGCACAAAAT | 9873 |
rs181431934 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991485 | ACTGGCAAACCAAAT[A/C]CAGCAGCACACCAAA | 9873 |
rs181432454 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000713 | TATTGTGAAACTAAG[G/T]AGATCTATGTACTTG | 9873 |
rs181452832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958421 | TATTTGGGAGGCTGA[C/G]GCAGGAGAATCACTG | 9873 |
rs181454747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989743 | ACACACCGGGGCCAA[G/T]CAACACTGCCTCAGG | 9873 |
rs181477592 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045019 | AGGTTGCAGTGAGCC[A/G]AGATCGCTCCACTGC | 9873 |
rs181477925 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904790 | TCATATACTAGTTTC[G/T]TCATCTATCTCTCCT | 9873 |
rs181481128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918001 | TTGGGGAATATTACA[A/G]TATTAGCAACATGAA | 9873 |
rs181488848 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980785 | ATATACATCTCACTC[C/T]CTTCTACCATATTGA | 9873 |
rs181490441 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027435 | AGCAGCAAAGCATTC[A/C]AAATGTAACCTGGCT | 9873 |
rs181490623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937411 | AGCATTTAGCAAGAA[A/G]TATAAAGCCTTAGTG | 9873 |
rs181496436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132071 | TCTGGGATTTTCTTA[C/T]AAGATTGCTGATACC | 9873 |
rs181497343 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009220 | CATACTACAGGCTGG[A/G]TGTGGTGGCTCACGC | 9873 |
rs181502117 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865976 | GTTCATCTTCAGTTT[G/T]CCCAGGAAGTAAGTA | 9873 |
rs181505512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083463 | CTGACACAGGAGAAT[C/T]GCTTGAACCTGAGAG | 9873 |
rs181515227 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882030 | GGCGCCTGTAGTCCC[A/G]GCTAGTTGGGAGGCT | 9873 |
rs181527132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127207 | AACACCAGAAATAAC[A/G]TTTTCTTATTAAATT | 9873 |
rs181562425 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017731 | TTCATAATGCTCCCA[C/T]TGCATGAAAATATCT | 9873 |
rs181574020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978622 | CTGGATTATAGGAGC[G/T]ATTTCCCTGATGCTG | 9873 |
rs181590527 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063313 | TGGAAAGGAACAACC[A/G]GTACCAGCCACTGCA | 9873 |
rs181624383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869728 | AGAGATCAAGAGTGA[C/T]AAAGTCTGTTTCCTT | 9873 |
rs181640042 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885865 | TTCATTGTACACCCT[A/G]CCCTCCTCACTATGG | 9873 |
rs181660842 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010979 | TTGGTGGTGGCTGTG[A/G]GGGGGTGGGCAGCTC | 9873 |
rs181667824 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945890 | TCATTAGAAAGTCAG[G/T]AAACAACTGGTGCTG | 9873 |
rs181691094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909796 | AGGAGCACCTCTGCC[C/T]GGCCGCCCCGTCTGA | 9873 |
rs181717233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846783 | TCATACATGTTCATC[A/G]TAGAAAAGCTGGAAA | 9873 |
rs181721870 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874480 | CAGGTGCGAGCCACT[A/G]TGCCTGACCTCTAGT | 9873 |
rs181728041 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134456 | GCTTGGGTGACAGGG[C/T]GAGACCCTGTCTCAA | 9873 |
rs181759893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001533 | ACTGAGGCCCAGAGA[A/G]ATTTTAGAGTATCAC | 9873 |
rs181786694 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055737 | ACAATCTGTAGAGTA[C/G]AAAAGCAGAAATATC | 9873 |
rs181787878 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889253 | GGCGTGAGCCACCGC[A/G]CCCGGCTATAATTAT | 9873 |
rs181793089 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018257 | GTTCCTGGCCCAGAC[G/T]TGAAATAAGCTAGTT | 9873 |
rs181799148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092159 | TAGAGGTAGGGTCTT[G/T]CTCCATCACTAAGGC | 9873 |
rs181805737 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996792 | AACAAAATACATTTT[A/T]AAAAAACTGCCAGCA | 9873 |
rs181817308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925601 | TTTGTTGCCACGGTG[C/T]ATTTCACTTCAGCAA | 9873 |
rs181827318 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890232 | TGGACTTATCTTTCC[A/G/T]AGTGGGAAGGAAGCT | 9873 |
rs181831271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936091 | ACCACTTACTAGCAA[C/T]CATCACTCTGGGAAG | 9873 |
rs181836447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955477 | GCATAATTGGTTACA[C/T]CACTGGCTAATGGTG | 9873 |
rs181837297 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910435 | TGTTACTGTGTCTGT[A/G]TAGAAAGAAGTAGAC | 9873 |
rs181837962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854489 | CAAGCTGGAGTGCAA[C/T]GGTGCGATCATAGCT | 9873 |
rs181839815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926394 | GGCATGACCAGTTGC[A/T]GAGAGGAGTATTCTC | 9873 |
rs181841793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094740 | TTTATTATCAGCAAA[C/T]TGATAATTGTTTAAT | 9873 |
rs181847422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104016 | AATACAAATAAATGT[C/T]TTCTGTTATTAAACC | 9873 |
rs181855206 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074079 | AGTACTTAAAACAGT[G/T]TGATATCGGGAAAAA | 9873 |
rs181855299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126668 | TGTTTACCAATATTA[A/C]TGAATCATTAAATTT | 9873 |
rs181924570 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930840 | GTAGGGATGGCTAAT[C/G]GGTACAAAAAAATAG | 9873 |
rs181927956 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900675 | AAAAGCTGATTTGAT[A/T]AAAAAAAAAAAGCAC | 9873 |
rs181928289 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009514 | AAACAAAGTCATACT[A/G]GAAAAAATTAAATAT | 9873 |
rs181930369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950930 | TCTCTAATTCAGTGT[G/T]AACAGAAGTAACATT | 9873 |
rs181938995 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082484 | AATTAGTTCTGTCTA[C/G]CTTTCAAGGAATAGG | 9873 |
rs181948780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894671 | GTATTCCAACTACAC[A/G]TTTGTACAGGTTCAC | 9873 |
rs181951898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914248 | TTGAACTCCTGACCT[A/C]AAGTGATCTGCCCAC | 9873 |
rs181954327 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046037 | ATTTTGTCACCTAGG[C/T]TGAAGTGCAGTGGCA | 9873 |
rs181961231 | snp | A/G | 0.000165645 | 0.00909918 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838819 | ATTTCCACATCTTCA[A/G]TCTTCTCTGCTGGCC | 9873 |
rs181968071 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099021 | GAGTTCAAAGCCAGC[C/T]TGGCCCACATAGTAA | 9873 |
rs181974029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877337 | TTCAGGCCAGTAAGA[C/T]GGAGGTTCTGCTTAA | 9873 |
rs181975849 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059107 | AAACAAGAAAATGAG[A/T]CTACTTTCAGTGAGA | 9873 |
rs181976528 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859677 | AGAAGAGAGAGATGC[A/G]CAGAACTTAGGAAAT | 9873 |
rs181976872 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885242 | GGAAACCAAGTGAGA[G/T]TATTTTATGCTAACA | 9873 |
rs181978805 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079246 | CTGTTGCCCAGGCTG[G/T]AGTGTGGTGGCCTGA | 9873 |
rs181984515 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968648 | TGATTTCCAAAATGA[C/T]AGTGCTGGCATGGAA | 9873 |
rs182007133 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986085 | CCTCTTATTTTTCTA[A/G]CAAGAGAAAACATTC | 9873 |
rs182020883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040895 | AAACTGCTCCCCCCC[C/T]TCTTTGGTAACTATC | 9873 |
rs182034340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023252 | CAAAGAGAATAAAAA[G/T]ACAAGCTGCAGATTA | 9873 |
rs182039275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005465 | ACTTGGCTTCCAGGA[A/C]ATCACTCTCCCTTGG | 9873 |
rs182046529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035955 | CAATCTCTTGACCTT[A/G]TGATCCGCCTACCTC | 9873 |
rs182064182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117962 | ATATGCACACATATT[A/C]TATATACATTTTCTG | 9873 |
rs182067434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073024 | ATGTTTTCCTGCTCC[C/T]TCTCTCCAGCCACAG | 9873 |
rs182083298 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850514 | GCCCACCACCACGCC[C/T]GGCTAATTTTTTGTA | 9873 |
rs182092878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118595 | CATAATTCACTCATT[C/T]TTATTGCTGAATGGT | 9873 |
rs182094043 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066395 | AGGACCATAAAAATC[C/T]TAGAAGAAAACCTAG | 9873 |
rs182098294 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118861 | ACTTACCCAAGGTCA[C/T]ACAACTAGGGGAAAA | 9873 |
rs182102151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135868 | AAGATAAGAACTGGG[A/G]ATTAAGGGGTGCGTT | 9873 |
rs182145962 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922069 | TATTAATAATAAATG[C/G]ACAAAAGATACAGAT | 9873 |
rs182153195 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850758 | TACTGACTGACAAGG[C/G]CCTCTAAATTTTAAC | 9873 |
rs182166562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886615 | TGTCTACCTCCATAC[C/T]CCTTCACCACATTGC | 9873 |
rs182204251 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887154 | ATATCTAAATTGATA[C/T]ATATACATCATTTTT | 9873 |
rs182208123 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027649 | GAAGCCAAATGTTAA[C/T]AGCCAAAACAATGAA | 9873 |
rs182222664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070264 | GCCTCTTATATGGCA[C/T]AGGCCCTGTCTGCTC | 9873 |
rs182232673 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064117 | CAATCAAACTAGAAC[G/T]CAGGATTAAGACACT | 9873 |
rs182234585 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908602 | TGATATAATATCTTA[C/T]TGTAGTTTTGATTTG | 9873 |
rs182243265 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922594 | GATTAAGCTATGATG[A/T]GTACTGTCACCAAAA | 9873 |
rs182244532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946654 | TATTGTGGAAGTATC[C/T]AGCATATTTTACCTT | 9873 |
rs182249473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997783 | TCGACTTCCTGCAAT[C/T]TCTACCTCCTGTGCT | 9873 |
rs182253972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975325 | ATATATCCAGCAGTA[C/G]AGAGTAGATTGGTGG | 9873 |
rs182254359 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851588 | TATTAACAAAAAAAC[A/T]AAAAATTAGCCGGGC | 9873 |
rs182264940 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870761 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGTGCCT | 9873 |
rs182265472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990093 | TCTAGAAGATTCTGC[A/G]TGGACAGATAAAAGC | 9873 |
rs182266336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953398 | TCTACATTTGGAAAA[C/T]AAATTCTCTCTCTTA | 9873 |
rs182268551 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032756 | CTGTAACGAGAGGTG[A/G/T]GGTGCAAGTGGGAAC | 9873 |
rs182268826 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053787 | TTATGACTATAGCAG[C/T]GATTCTCTATATTAA | 9873 |
rs182272751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138992 | TTAAAATTGTAATTT[G/T]CAGTCAGAAAACAAC | 9873 |
rs182279750 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014932 | CAATGCAACCTCTGC[C/T]TCCCAGGTTCAAGCA | 9873 |
rs182284608 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967124 | AGAATGGCGTGAACC[C/T]GGGAGGCAGAGCTTG | 9873 |
rs182304489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964842 | TTGCCCAGGCTGGAG[C/T]GCACTGGCAGGATCT | 9873 |
rs182313755 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994716 | GCTTGCAGTGAGCCG[A/G]GATCATGCCACTGCA | 9873 |
rs182320430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102950 | ATACACAACATGGAT[A/G]AATCTCAAAAACATT | 9873 |
rs182331082 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124259 | ACACCAGGGCCTATT[A/G]TGGGATGGGGGGACG | 9873 |
rs182374528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135728 | TTAGTTGTCTTTTCA[C/T]CTCAAACTTCACTCC | 9873 |
rs182405550 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908311 | GGTTGCTTCTAAATC[A/T]TGGCTATTGTGAATA | 9873 |
rs182417969 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869363 | ACAGATGCTAATTTT[C/T]CACTTGAAGCAGGGC | 9873 |
rs182423745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107230 | CAGCTAAGTTTTGTA[G/T]TTTTAGTAGAGACAG | 9873 |
rs182424320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972540 | ATAACTTCCCTTTTA[C/T]CTGCTTTATATATAA | 9873 |
rs182429206 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861160 | AAACCTCTAGCAGAA[C/T]GATCAGAAGAGAGGA | 9873 |
rs182430195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878168 | GTTGTAGTCACAACT[A/G]TTTTGGAGGCTGAGG | 9873 |
rs182436006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870075 | GCTTGCGTGCCTGTG[A/T]GCGTGCCAGTCCCTC | 9873 |
rs182441899 | snp | C/T | 0.0437281 | 0.141251 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73142813 | CTGCCTGCCTTTGCG[C/T]GTGTGTGTGTGTGTG | 9873 |
rs182443796 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133536 | CCCAGCACTTTGGCA[G/T]GCCAAGGCAGGTGGA | 9873 |
rs182456524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112647 | GCCTTTTTGTTGTTG[G/T]TGGTGGTGTTGGTGT | 9873 |
rs182472858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943365 | TTCAACTATAGTTAG[A/G]ATTAACTGAGGACTA | 9873 |
rs182480660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915674 | AATACAAAAATTAGC[C/T]GGGCGCGGTGGTGGG | 9873 |
rs182498339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986740 | AATCCTAATATACTT[A/C]TTGTGTAGTATTAAG | 9873 |
rs182498829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965299 | TACTTGGAAAGTTCT[C/T]CATTTGCCTGTCTTC | 9873 |
rs182509033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843767 | CTCAAGAGGCAATGA[C/T]GTTCAATGAACAGAA | 9873 |
rs182512810 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088986 | CCTTGATGTGCATAT[C/G]AACTAATTTAAATAT | 9873 |
rs182518328 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053928 | AAAAATTTTAACCAT[A/G]TATTTTTTACTCATC | 9873 |
rs182519872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923342 | ATTGCTCGGTCATAT[A/G]ATAACTCTATGTTTA | 9873 |
rs182521085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024235 | ATCCAATTGTATTAC[A/C]AAATGTGAGACATAA | 9873 |
rs182522258 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070486 | TGGAGTGCAGTGGCA[C/T]GACCTTGGCTCACTG | 9873 |
rs182526176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878905 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 9873 |
rs182528664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943793 | TGATATTTTATTAGT[G/T]CATTAACTACAAGAA | 9873 |
rs182532144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120938 | ACATAGGCTCCCCAC[A/G]AAATCTAATCTGGCA | 9873 |
rs182533272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006972 | TCTCAGTAACAATGC[C/T]GAACATTAAAAAGGG | 9873 |
rs182538621 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988002 | ACATCAAGTCCTTCA[C/T]GAATACTCACTTACC | 9873 |
rs182553797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908892 | CTCCTGGGCTCAAGC[A/G]ATCTGCCCACCTTGG | 9873 |
rs182566801 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012659 | ACAATAGCACCACCA[G/T]CCTCTCAGTTGCCTA | 9873 |
rs182573882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088664 | TTTTTTACACTCATG[C/T]TGTTTTTCTAAAATT | 9873 |
rs182575915 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872286 | CTTTTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 9873 |
rs182580884 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942396 | TTATATTACCCAGCC[C/T]TGTGTATTTCTTTAA | 9873 |
rs182584771 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953628 | AGACACTGCATGGGG[A/G]AAAAAAAAAACACAA | 9873 |
rs182618666 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133132 | ATGCACTGGCCATGA[C/T]GTGGAGAAATAGGAC | 9873 |
rs182644421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074548 | GGTGGACTTTAGGAT[A/G]GCAATATACCCTTAA | 9873 |
rs182651788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050452 | ATTACTATAAACATA[C/T]ATGGGACGGGTCACC | 9873 |
rs182652041 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096356 | GACCAGCCTGGCCAA[C/T]ATGTTGAAACCCTGC | 9873 |
rs182661874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085237 | TTTTTTTTTAAATGT[C/T]TATTCAAAAAAAGTC | 9873 |
rs182679253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848556 | TAACCCTTCATAGAT[C/T]GTCCATTCCTAGAGG | 9873 |
rs182697946 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910812 | GAGAAACACCCAAGA[A/G]TGATCAATAAATACT | 9873 |
rs182699348 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867482 | CACTTAAGATTTTGT[A/G]CAAATCTCTGGATGT | 9873 |
rs182709180 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129906 | TTGAGACAGAGTCTC[A/G]CTCTGTCGCCCAGGC | 9873 |
rs182723977 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934214 | TGAAGATGCATCTGT[A/C]TCTTGTCTAGCATTT | 9873 |
rs182725545 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999876 | AATCAGACACACACA[C/G]ACACACACACAAACA | 9873 |
rs182736697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899519 | AGGAGGATCTTTTGA[A/G]CCCAGGAGTTCAAGG | 9873 |
rs182752486 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934418 | TCACTGCAACCTCCA[A/C]CTCCTGGGTTCAAGA | 9873 |
rs182761531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863208 | TTGGGATTACAGGCA[C/T]AAGCCACTGTGGCAG | 9873 |
rs182833308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927060 | TCCTAGTTTTTACTA[C/T]CTTAACAATTCACAA | 9873 |
rs182833359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883155 | ATGACCCTTAACTCA[C/T]ACCAGACCTCAACAA | 9873 |
rs182835402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905603 | AGCCCCCCACCCCCC[G/T]ACAGGTCCCAGTGCG | 9873 |
rs182862047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856121 | TTACATTAATTAATT[A/G]AAGTATCAAATATCT | 9873 |
rs182862834 | snp | A/C/G | 0.00119752 | 0.0244452 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111702 | TTCCTTTTAGTGAAG[A/C/G]TGATTTTCTCTGGTG | 9873 |
rs182866364 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872131 | TACGTCTTTATATAA[A/G]ACAATTGGAATTTTT | 9873 |
rs182903177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123679 | ATACGATCTTCTTAA[C/T]TGCATAACCATCCCC | 9873 |
rs182916806 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081127 | AATAATAAACATGTC[C/G]TATTTACTTGATTAA | 9873 |
rs182923281 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102102 | TTCATTAAAAACTTA[C/T]CCAAATAATTGGTAA | 9873 |
rs182954713 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080595 | TCTCATTTATTATAG[A/G]TAATCAAGTGATAAT | 9873 |
rs182963334 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015676 | AAATTTTGATAATTT[C/T]GAAATTATATCCGAA | 9873 |
rs182967548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920113 | TAAACTGTAAGACAG[C/T]AGAAATAATGAATAT | 9873 |
rs182969082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042221 | TGCGCCACTGCACCC[A/G]GCTGAGATTATTTTT | 9873 |
rs182971398 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122460 | TCCTGCACAAAGGTA[A/G]CACCACTTAACCATC | 9873 |
rs182991888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842452 | ACATTCCACAAGGGA[C/T]TGACTGACAAGTCTC | 9873 |
rs183007295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891018 | AACCTCCGGGCTCAA[C/G]TGACTCTCCCACTTC | 9873 |
rs183045873 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127824 | TGGGTGCAGTGGCTC[A/C]AGCTGTAATCCCAAC | 9873 |
rs183048980 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084306 | ACAAAACAATGTACA[A/C]GGCCACTACAAATTG | 9873 |
rs183051783 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855644 | ATGTAACACAAGGAG[A/G]ATAATTTTTTAACCC | 9873 |
rs183056692 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106361 | CAGTGAGCTGTGATG[A/G]CACCACTACACTCCA | 9873 |
rs183063407 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002070 | TCATCTCCTGAGATT[G/T]CCCTTTTGTGGGAAA | 9873 |
rs183070081 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981467 | CCAATAGAAAAAAAA[A/T]AGGATTTTATTTTTG | 9873 |
rs183079493 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983288 | GACAGAGCGAGACTC[C/G/T]GTCTCAAAAAAAAAA | 9873 |
rs183084863 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961676 | TTTCAGAGCAAGTTA[C/T]TAAATATACTAGCCT | 9873 |
rs183086221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912594 | GTTTTTATTTTTTGA[A/T]GTGTCTTTGTCTGAT | 9873 |
rs183087190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010398 | TTCCAGGATTTTGTA[A/T]ATTTGTTTTTTATTG | 9873 |
rs183089634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959150 | TCTGTCAATACTCTT[C/T]ACCCATTTTAGAAAT | 9873 |
rs183093778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037306 | CATCTGAAGTCCATG[A/G]TTTACACTAGGATTC | 9873 |
rs183096908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018938 | TATGAGGGTTCAATT[A/G]AGTCAAGATCTCAGA | 9873 |
rs183100428 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949389 | CTGGAGGCAGAGGTT[A/T]CAGTGAGCCGAGATC | 9873 |
rs183105172 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939295 | TGACAGTAATTCCCC[A/C]CTAAAAATTGTAACT | 9873 |
rs183106982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020217 | TTAACAAGTGAAGAA[A/G]CACAAAGAGAGCCAC | 9873 |
rs183107250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876856 | GCATTATTATTATAT[A/C]TACGTCCAGGATTTT | 9873 |
rs183108949 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065307 | GACAAAATTAAACAG[C/T]GCTTCATGCTAAAAA | 9873 |
rs183110218 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037677 | GTGGCCATTTAATCA[C/T]ATAAGTCAGATATAG | 9873 |
rs183114142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002890 | TAATTGTTTATTAAC[A/G]TCTGTCCCTCTCACT | 9873 |
rs183114198 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856708 | ATCATCAGTCAGTTC[A/G]GTGGCAAAACAGTCT | 9873 |
rs183117270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047528 | AATACTGGTCATTGA[C/T]AGTACCTAGCCACTG | 9873 |
rs183117431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028794 | GTCTCATGATAGTGA[C/G]TTCTCATGAGAGCTG | 9873 |
rs183123969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002576 | ACTATTAATTTATAC[A/T]TAAAATACATTTTAA | 9873 |
rs183129175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893474 | CATATGCCATCACAC[A/G]CAGATAATTTTTTTG | 9873 |
rs183129847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888124 | AATAAGAAAACAAGA[C/T]AGCCAAGTATAGGAA | 9873 |
rs183170315 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851825 | CTCAATATCACTAAA[A/G]AAATGCAAATCAAAA | 9873 |
rs183172658 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960352 | GATCACATTTCAACA[C/T]GCAATTTGGAAGAAA | 9873 |
rs183174428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843387 | TAGACAGGGCACAAC[A/G]AAGACCAAAACAAAC | 9873 |
rs183209096 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056405 | GAACACTGCTCATAC[A/C]CCCAAAATGTAATCT | 9873 |
rs183224290 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919253 | CTCTTCTGGTACTTG[A/G]AACAAAAGGGCACTA | 9873 |
rs183226014 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032920 | AATCAAGCTTGCGAG[A/C]AGTGCAGTGCCATTA | 9873 |
rs183242385 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061412 | CTAGCTGCAGGAATT[A/C]TTTTTTTCCATACCC | 9873 |
rs183244284 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861737 | GAGTTCAAGACCAAC[C/T]TGACCGACATAGAGA | 9873 |
rs183249206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878282 | GAAATATATTGAGAC[A/C]CTGTCTCTAAAAATA | 9873 |
rs183251833 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998697 | TAGTGGAGGAAAAAA[A/T]TGATAATAAAAAATA | 9873 |
rs183262581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898865 | TTCCTGAGTAGCAGG[A/G]ACTACAGGTGTGTGC | 9873 |
rs183266272 | snp | A/G | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140212 | TACATCTGTCAGAAT[A/G]TGTCTCTTGCTCGCC | 9873 |
rs183270202 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099836 | GAGAGGCGGCACCAC[A/C]ATTTTCTTCCCACCT | 9873 |
rs183283548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875583 | ATCCTTCCGCCCTCC[A/T]GCCCTGGCCTCCCAA | 9873 |
rs183300556 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129501 | ACTGCACATGCAAGG[C/G]ATCTAGGTTGCATGC | 9873 |
rs183317811 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73141150 | AGCGGGGAGACTGAT[A/G]ACAAGCCGGGTGCAT | 9873 |
rs183343329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948373 | TCAAAATTACTGAAT[A/G]TTTCATTTTTCAACA | 9873 |
rs183351214 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876443 | GCAGCAACAGATTAC[C/T]GTGTTTGAACAACAT | 9873 |
rs183373687 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911073 | CTTTGCCTAGTCCTA[C/T]GTCTTAGAGAGTTTC | 9873 |
rs183376673 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019465 | CTATTTTTTTAAATT[A/G]TGAAATTAATTTGTT | 9873 |
rs183420678 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938559 | TTTGCAAGGTGTCCT[C/T]TTCCTGACTGAATGA | 9873 |
rs183442868 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915158 | AAAACTCAACATCAC[C/T]GATCATTACAGAAAT | 9873 |
rs183444141 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982420 | GTGTGTGTTTGTTAG[A/T]CATTAAGAACAATAC | 9873 |
rs183446404 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933861 | TGCCTGCAATTTCAA[C/G]ACTTTTGGAGGCTTA | 9873 |
rs183448004 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975006 | AAGATGAGTTATATA[C/T]GCCTACATATGAATG | 9873 |
rs183453164 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057136 | CATAGGTTGACAATT[C/G]ATTTGCATCGTGAAG | 9873 |
rs183453698 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952782 | AGGCACTTACACATA[C/T]TTACAATTCATGAAA | 9873 |
rs183477087 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096631 | TCAAACACAAGAGAA[C/T]AGCAATGGTAAAAAG | 9873 |
rs183480670 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136247 | AATTCTATTTACAGT[C/T]TAATGTGCTGTAGAT | 9873 |
rs183496026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024687 | ATCAAAAGAAACTAT[C/G]AACAGAGTAAACAGA | 9873 |
rs183499592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991987 | TCCCTGTTTGTAGAT[A/G]ACATGATTGTTTATT | 9873 |
rs183503641 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007495 | AAGCATGGTGGTAGT[G/T]GTGGCTATGCAGGAG | 9873 |
rs183514223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061861 | CAGAGCACTTGGGGA[A/G]AGGGGCAGCTGTGGG | 9873 |
rs183523300 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043309 | ATCACTAAAAGGCTC[A/G]GTCAAGTAGTGAAGA | 9873 |
rs183547931 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853447 | GGAGACAGAGTCTCG[C/G]TCTGTTGCCCAGGCT | 9873 |
rs183560554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888914 | GGCGTGAGCCACTGC[A/G]CCCAGCCAAACATAT | 9873 |
rs183573794 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927995 | CATTTATAATTAGGG[A/C]AAGTGGGAGTACCAC | 9873 |
rs183602278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892067 | ATCTCAAAGAGAATG[A/G]ATTTGTAGGGAGTAG | 9873 |
rs183603895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137231 | GAAACCTAAACTCTT[A/G]TTTTAGTAGGTAATA | 9873 |
rs183666875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011422 | GCCCCAGCACCACTC[A/G]CTCCCCAGCAGCACT | 9873 |
rs183679967 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970328 | ACAATCCAGTGAGTA[A/G]AAATACTTACAATTC | 9873 |
rs183682027 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120590 | CAAAATTAGCCGGGC[G/T]TGGTGGTGCATGCCT | 9873 |
rs183684314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075083 | ATCATCAGGAAAGTG[C/T]AAATCAAACCCACAA | 9873 |
rs183686924 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909209 | GCCTGACTGGTTTTT[A/G]TATTTTTGGTGGAGA | 9873 |
rs183690873 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098426 | CTTTATATGATTTTG[A/G]TCTTTTAAAATTAAC | 9873 |
rs183692622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924524 | CCTGATCTCGTGATC[C/T]GCCCACCTTGGCCTC | 9873 |
rs183693329 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905481 | TCTAGGGTACATAGG[C/T]ACAACGTGCAGGTTT | 9873 |
rs183699941 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038579 | GCAACGATTATCCTA[A/G]GCAAACTAACACAGA | 9873 |
rs183703429 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944384 | TCAATAAATTAGGTA[C/T]TGATGGGACGTATCT | 9873 |
rs183714081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937819 | CCTAGACAAACATGA[A/G]GTTTAAAAATGATTT | 9873 |
rs183725018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119962 | CAGTTCCACATGGCT[A/G]GGGAAGCCTCACAAT | 9873 |
rs183746625 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969365 | ATTAGAACTGTGCAG[A/G]AAAGCTAGTTGGCAT | 9873 |
rs183749768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866910 | AGTTGGGAGGTTAGA[C/G]TTTTAGCTTTTAGTT | 9873 |
rs183778210 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017245 | TGTCCTCCCAAAGTT[C/T]TGGGATTACAAGTAT | 9873 |
rs183787235 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999663 | CAGTTAAATTCAGGT[C/T]TGAGATTACTTCATC | 9873 |
rs183792793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978359 | AAAATAAAAATGAGC[A/C]AAAAATCTGAATAGA | 9873 |
rs183812781 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925257 | CCTTACCATAATCAG[A/G]ATCATTTCTGATTAT | 9873 |
rs183818421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048315 | TACCTCTGATCTCCC[C/T]TAAGCCAAGGTTCAT | 9873 |
rs183821478 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944939 | TTCCATGCTCACGGG[A/T]AGGAAGAATCAATAT | 9873 |
rs183830121 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071560 | AAAAAAATTAGCTGG[A/G]CATGGTGGTGTGTGC | 9873 |
rs183834907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055058 | AAAAGGAGGAACAAA[A/G]GCTCATCCTACCTGG | 9873 |
rs183838938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034106 | TTATACTTTAAGTTC[C/T]GGGATACATGTGCAG | 9873 |
rs183875624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084683 | ACTGGCATGGGCCAA[C/T]GTGCTTAGCCAGTAC | 9873 |
rs183894886 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992508 | CCTGACTTCAAACTA[C/T]ACTACAAGGCTACGG | 9873 |
rs183914914 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918478 | ATGTTAGCAGAGGAA[G/T]ATTTCAGTCTTTCAT | 9873 |
rs183940938 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959220 | CATATATCCAGCAGT[C/T]TTTTTTTTTTTTTTT | 9873 |
rs183941106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847581 | AAAGCAGTACTATAT[A/G]AAAGGACATTTTTGT | 9873 |
rs183946797 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091367 | AACATGGTGAAACCC[A/C]ATCTCTACTAAAAAT | 9873 |
rs183947373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989448 | AAAGAATAAGGCAAT[A/T]CTGTATTTCCCCATA | 9873 |
rs183949153 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882238 | ATGAGGTCAGGAGTT[C/T]GAGACCAGCTTGGCC | 9873 |
rs183957437 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967882 | GGATCACGAGGTCAG[A/G]AGATTGAGACCATCC | 9873 |
rs183978829 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044847 | AGGCCGAGGCAGGTG[C/G]ATCACGAGGTCAGGA | 9873 |
rs183979932 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027060 | ACCGAGAGACATGGC[A/G]TATTTCTATAAAAAT | 9873 |
rs183983718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008971 | TAAGCTTACTTAAAA[A/G]TCATTAGAGAGCTGA | 9873 |
rs184004249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900518 | TGTGGAAAATAGCAA[C/T]GATAAAATAACATCA | 9873 |
rs184009962 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032397 | CCTGGTTAATTTTTT[A/T]AATTTTTTTATAGAG | 9873 |
rs184011946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065852 | CTCAAGGAAATAAGA[C/G]AGGACACAAACAAAT | 9873 |
rs184017080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029234 | GAAAACAAAAGATAC[A/G]GAAACCACTTACAAG | 9873 |
rs184017366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72844000 | GCAACAGAGCGAGAC[C/T]CTGTCTCTAAAAAAA | 9873 |
rs184030487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106476 | CTCTTAAATCAGTAT[A/T]CTGCTTGTTAAAGAA | 9873 |
rs184038970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879551 | ACATGAAGATAAATA[A/G]GAATGAACTAGAAGA | 9873 |
rs184039673 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863891 | GTTGATGTAATTGTA[A/C]AATGGTATAACCACT | 9873 |
rs184043683 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069352 | ACAAAATAACTATCC[A/G]AAGAGAAATTTAAAA | 9873 |
rs184050819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923776 | GAAACCCCGTCTCTA[A/C]TAAAAATACAAAAAT | 9873 |
rs184061634 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864611 | TTGTCAATTAAAAAA[A/T]AAATAAATAAGAGTA | 9873 |
rs184077037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965784 | TGCATGTTCTTAAGT[A/G]TATAAATAGAATCAC | 9873 |
rs184080953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996912 | TGTTTTTCCTTAGGG[C/T]ATTTGTTGAATCATG | 9873 |
rs184085547 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994333 | CAGGTGCTATGTTTC[A/G]TACTTTACAGGTATT | 9873 |
rs184090852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888535 | ATAGGTATCAATAAA[C/T]GAAACAGAAAAAAAG | 9873 |
rs184095645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971744 | GCCAAGGTGACATTT[C/G]GATTTTGGCCTTGTG | 9873 |
rs184100530 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116256 | CCCAATTTCATTATT[A/G]CTTAATTTTCTTATA | 9873 |
rs184105479 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949408 | TGAGCCGAGATCATG[A/C]CACTGCACTCTAGCC | 9873 |
rs184109355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921374 | GCTGTCAAAGAATGA[C/G]AGCATATAGATAGTA | 9873 |
rs184115010 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091904 | AAATTAGCTGGTAGC[A/G/T]TGCACCTGTAATCCC | 9873 |
rs184117614 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029986 | AATCTGATGTCCAGA[C/G]TCACCACCTTATTAG | 9873 |
rs184118909 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011847 | TTTCCTGTCACTTTT[A/C]TGTTGAATTCCAGTG | 9873 |
rs184135260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885302 | AAAACTGAGAAAACG[A/G]ATCTGCTACAATGGT | 9873 |
rs184135454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929584 | CCTGCCTTAAATTGC[A/G]ATTGTCTGAACCAAT | 9873 |
rs184138637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907342 | CTTTCTCTTGCCTGA[C/T]TGCCTTAGCCAGAAC | 9873 |
rs184154871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052728 | TTTTAATAATCTTCA[C/T]ACTTGTAAGAAAGGG | 9873 |
rs184156001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850367 | ACTGCACCAGGCCTA[A/G]GACAGAGATTTTTTT | 9873 |
rs184166241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988067 | ACAAGTTGCTTATAA[A/G]GTTGCTTACATTTCT | 9873 |
rs184170588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014800 | GGACAACTCCTGAGC[A/G]TAAAAGATAATAAAT | 9873 |
rs184171222 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040415 | AAACACATACACACA[C/G]ATACACATTTGTATG | 9873 |
rs184185068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126057 | AAGACAAAAGAATTC[C/T]ACGGCCAGGTGCGGT | 9873 |
rs184195207 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087719 | CAAAAAAAAAAAAAA[A/T]ATTTTTAAAATAAAT | 9873 |
rs184198940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077225 | TAAGAAACCAAACAA[C/T]CCAATTTAAAAAAAA | 9873 |
rs184212589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943916 | ACTATTAAATACTCA[C/G]ACTTTAATCATTATT | 9873 |
rs184213415 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045854 | AGCCACCAGCATGGC[A/T]CATGTATACATATGT | 9873 |
rs184216272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027574 | CCATGAGGTAGAAAA[G/T]AAAAACCAATTTTCT | 9873 |
rs184231701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134310 | ACCCTCTCTCTACAA[A/C]AAATACAAAATTAGC | 9873 |
rs184234438 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082164 | AACAGGGTGAAACCC[A/G]GTCTCTACTAAAAAT | 9873 |
rs184235898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872464 | GCCCCCTATTCCCTG[C/T]AGTCTTGACAATCAC | 9873 |
rs184237359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103174 | GTGTAGTAGTGTTTA[A/G]TCAACTACATATAAT | 9873 |
rs184243700 | snp | A/C/G | 0.00279242 | 0.0372774 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909059 | TCCCTTCCCCTCCCC[A/C/G]CTCCATCTCTCCGGT | 9873 |
rs184244757 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846244 | GGAGTGCAGTGGTGC[A/C]ATCTCGGCTCACTGC | 9873 |
rs184247422 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063386 | CTGCATCAACTAATG[A/G]TCAAAACAACCAGCT | 9873 |
rs184254412 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938183 | ATGAAGGAGTTTTTT[G/T]TTTTTTTTTTTTTTT | 9873 |
rs184306165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058390 | TGTGACATGGTATGG[C/T]TAGATGTCATCACAA | 9873 |
rs184314338 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021923 | AAATAATAAAAAAAA[A/T]TTTCCAGGCCTGGTG | 9873 |
rs184358381 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062611 | TGACCCGATGGAGCT[A/G]AAATACACAGCACGA | 9873 |
rs184367755 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040892 | CACAAACTGCTCCCC[C/G]CCCTCTTTGGTAACT | 9873 |
rs184371163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023192 | AAGAAAAATGATAAA[C/T]TGGACCTTATCAGAA | 9873 |
rs184373248 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025777 | CTTATGACTAAGAAT[G/T]TTTTTAAAGCTATAT | 9873 |
rs184374741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051256 | GGGGATTGAGGCTAC[A/G]GTGAGCCAAGATTGC | 9873 |
rs184379086 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066677 | AAAGTAGGCAAAGGA[C/T]ATGAACAGACAGTTC | 9873 |
rs184380496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865051 | TTCCTTCCTTATTCT[A/G]TAAGGGAGTAGTCTG | 9873 |
rs184399276 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916835 | TACTTGTGCTTTCAA[C/T]GTCAAATCTGAGAAT | 9873 |
rs184415678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956136 | TGGAGCAATTTGAGC[A/G]TAAAAATAAATAGTA | 9873 |
rs184431474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881564 | AGGAAAGGAAATCAG[C/T]GTATCAAAGTCATAC | 9873 |
rs184437641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883702 | TCTGGGCGGCCAAGG[C/T]AGGCAGATTGCTTGA | 9873 |
rs184438309 | snp | A/C | 0.000222796 | 0.0105522 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72989034 | AGTATTTCTTTTTGC[A/C]TTTAGCTAAATCTTT | 9873 |
rs184449954 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838272 | GTTTCACTTTCTCAG[C/T]CTGGGGACTAACCTT | 9873 |
rs184452452 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877076 | TCCAGGCTGCCTCCA[G/T]TGCAGCCTCATCCTC | 9873 |
rs184454535 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906148 | TGACATAGTATCTCA[C/T]TGTGGTTTTGATTTG | 9873 |
rs184457700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858841 | AAGATGGAGTATCAG[A/G]GATCAGATTTAACCT | 9873 |
rs184478726 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108137 | TATCTCATTGTAGTT[C/T]TGATATGCATTTCTC | 9873 |
rs184487789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130472 | ACCATCAAGTTCAGG[A/G]GAGTATCCTCTATTC | 9873 |
rs184515736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134127 | CTCTAGACCAGATTA[A/G]ATTACCTCTAAGATC | 9873 |
rs184516482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081306 | GGGCATGGTGGCACG[C/T]ACCTGTAGTCCCAGC | 9873 |
rs184536470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936335 | GCTCTAAGTCTGTTA[C/T]CTTATCTATAAAATA | 9873 |
rs184549370 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008799 | GAATTGTGAAAGAAA[C/T]CACATGCAAACAAGC | 9873 |
rs184552304 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934961 | CTTTAAGCAGCCACG[A/T]CCTTTCCAGGTAGCT | 9873 |
rs184558868 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909440 | TGCTAAGATTACAGC[C/T]TCTGCCCAGCCGCCA | 9873 |
rs184570692 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903371 | ACAGGCGCCCGCCAC[C/T]GCGCCCAGCTAATTT | 9873 |
rs184575778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967392 | TGGGTAAACAAAATA[C/T]GGTATATCCATATCA | 9873 |
rs184579057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977341 | GGACAAATGGGATCA[C/T]ATCAAGTTAAAAAAC | 9873 |
rs184593267 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874116 | AATTTAATGTGCCTA[A/C]GTTTATCTTTTAACA | 9873 |
rs184633554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115452 | TGAGCCACTGCGCCC[A/G]CCCTATCTCACTGTT | 9873 |
rs184668340 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082103 | AGCACTTTGGGAGGC[C/T]GAGGTAGGCGGATCA | 9873 |
rs184687037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124853 | AGATAATTACAGACA[C/T]TATACTAGTCACATT | 9873 |
rs184690454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954371 | ATGCCACCATGCCTG[A/G]CTAATTATTTTATTT | 9873 |
rs184717545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854051 | TTAGGATGCTGTTAT[A/G]TATATTTTTAAAAAC | 9873 |
rs184719227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915860 | AGAAAATGTGGTACA[C/T]ATACACCACAGAACA | 9873 |
rs184720749 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845478 | AACAACAAACAAACA[A/C]AAACCATGGAGGTCC | 9873 |
rs184723847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852175 | ATTATAGGAGTGAGC[C/T]ATCATGCCTGGCTGA | 9873 |
rs184727292 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889080 | CTGCCTCAACCTCCC[A/G]AGTAGCTGGGACTAC | 9873 |
rs184731307 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895424 | CGTCTAACACTTTTG[A/G]GAACATACCTAGAGG | 9873 |
rs184740279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914303 | TACAGGTGTGAGTCA[A/G]GTGCCCAGCCTGCCC | 9873 |
rs184802273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102988 | AAAAGCAAATTACAC[A/T]ATTAAGTAGAAAATG | 9873 |
rs184807794 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063092 | AACAGTGGATGTCTC[A/G]GCAGAAACCCTACAA | 9873 |
rs184814935 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144332 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 9873 |
rs184817678 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120397 | ATGTCTCATTTGGTA[A/G]CAAACATTTCTTCAG | 9873 |
rs184834026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097368 | GGTTTGTTTGTTTGG[C/T]TTATTTTATTTATTT | 9873 |
rs184856359 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899759 | AAAAAAAAAAAAAAA[A/G]ACTTTTTAAATGATT | 9873 |
rs184858202 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966179 | AGCCTTTTTTTTTTT[C/T]CAGTTGGTCTCACTC | 9873 |
rs184871103 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021261 | AAACAGGCACACATA[C/T]GTTCACTGCAGCCCC | 9873 |
rs184871339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973142 | GGAGGCCAAGGCAGG[C/T]GGATCACCTGAGGTC | 9873 |
rs184875062 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003370 | TAAATGAATACATAG[G/T]AACAGCAGCAGAATT | 9873 |
rs184884281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984288 | ATAGGAATCCTACTC[C/T]TAGTTTGCAATTAAT | 9873 |
rs184892323 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931272 | ACTAATTTTTGTGGG[G/T]TTTTTTTTTTTTTTA | 9873 |
rs184895297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057947 | TGCAGTGGCACGATC[C/T]TGGCTCACTGCAAGC | 9873 |
rs184898790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076696 | AATGGTATGTAAATT[A/T]AAAGTATACATAAAA | 9873 |
rs184900038 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837690 | TGTGCAGGGTGCGCA[A/G]TCCTTCAGTCCTTTC | 9873 |
rs184901859 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951408 | CAGCAAACGAGAGCG[A/G]CAGATTACGCAGCTC | 9873 |
rs184909189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994751 | AGCCTGGGTGACAGA[A/G]CGAGACTCCATCTCA | 9873 |
rs184913275 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038764 | TACCTGGGTGATAGA[C/T]TCATTCATACTCCAA | 9873 |
rs184924083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962988 | CACTTAACTGCTTAC[C/T]TGTGTGAGCTGGCAA | 9873 |
rs184924455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139972 | CCTGGGGCTTGGTAA[C/T]TCAAAGGTTCTTTGA | 9873 |
rs184927960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122233 | GTGATTCAAATTTTA[C/T]GTTTTCATCAAAGAA | 9873 |
rs184930770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893702 | GCAGTGAGCCAAGAT[C/T]GTGGCACTGCACTCC | 9873 |
rs184952171 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857989 | GACCTCGTCTCTCTA[A/G]TGAAGACAGTTACTT | 9873 |
rs184957157 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896763 | ATTAGGGGGAAAATA[A/C]TAAAAAAAAAAAAAA | 9873 |
rs185013639 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977964 | GTGGCATATACACCA[C/T]GGAATACTATGCAGT | 9873 |
rs185022919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984930 | CTGGGAGGGAAAGTT[C/T]CTCCCTGAGTCAGTG | 9873 |
rs185024886 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940626 | GGCTCCCCGCCCCAC[C/T]CAGCCTGATAAAGCG | 9873 |
rs185025525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071220 | TTCCTAGTTTTGCAC[C/T]TCAGAGTTACAAAAA | 9873 |
rs185045639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009291 | ACTTGAGATCAAAGA[A/G]TTTGAGACCAGCCTG | 9873 |
rs185045994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913694 | ACTTCTGATTTTATT[A/T]ATTTGGTTATTCTCT | 9873 |
rs185050390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955147 | TCCCCACTTCAGATG[C/T]TAATTGGAAGTCTCA | 9873 |
rs185058316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999291 | TTCACAGACATGAGC[A/G]TTTGTTGAATCTTAC | 9873 |
rs185064989 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880591 | CCATATATAAAAGTC[A/G]GCTCAAAATGATTAA | 9873 |
rs185066689 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113522 | TACAAGCATGTGCCA[C/G]CACGCCCAGCTAGTT | 9873 |
rs185079300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902737 | ATTTTCTATACAAAT[A/G]AGAAATCATCCAACA | 9873 |
rs185081423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916379 | CAGTAGTAGCATGAT[A/C]ATAGCCTGCTGCAGC | 9873 |
rs185081838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876876 | TCCAGGATTTTAATA[C/T]ATTCATGATGAAATG | 9873 |
rs185115877 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849056 | TTACCAAACACTGCC[A/G]CCTTTTGGCTACACA | 9873 |
rs185127415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086238 | ACATGGCAAAACTCC[A/G]TCTCTACTAAAAATA | 9873 |
rs185142470 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090514 | ACAGGCGTGAGCCAC[C/T]GCGCGCGGCCTACAA | 9873 |
rs185156277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054643 | GGGAAACAAACAGAG[C/G]GGGTGGAGGAAAGAG | 9873 |
rs185161814 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134029 | ACTTTAAATGGGATA[C/T]GTAATCATATATGAT | 9873 |
rs185174319 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135773 | CAAATGCCATTCGCA[A/G]AACAAATGAACTGAA | 9873 |
rs185174560 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965111 | TTACTTCTTAATTCA[A/G]AGGTCTTTGATAGAT | 9873 |
rs185174791 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013088 | GAAACATTTCAACAC[C/T]TCCATTACGTTCTGA | 9873 |
rs185180048 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030434 | ACATAAATGTATCCA[A/C]GTGAGTATATAGTTT | 9873 |
rs185180656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995248 | AGCTGTTTTCCCCCT[A/C]AATTGTAATAGTACT | 9873 |
rs185187404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118711 | AGAATATGATGATAC[C/T]ATAATGATGATGGCA | 9873 |
rs185191355 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068363 | GGTAGGGTGGGGTTG[C/G]GGGGGCGGAGAGAGA | 9873 |
rs185197764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943548 | TTAATGAAAGGGAAG[A/G]AAATTGAAGAGAATG | 9873 |
rs185203016 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058841 | CCAAAGTGCTGGGAT[G/T]ACACGTGTGAGCCAT | 9873 |
rs185209328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031463 | GTGACAGAACAAGAC[C/G]CTGTCTCCGAAAAAA | 9873 |
rs185211439 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051919 | CACACACACACACCC[C/T]ACACACACTGACATC | 9873 |
rs185227205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868329 | CATGAGTGGGGGAGA[A/C]CAACACACACTGGGG | 9873 |
rs185227959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950202 | TGGGTTATTTGTTTT[C/T]ATTGAATTGTAAAGC | 9873 |
rs185231884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037389 | ATTACAGTATCATAG[A/G]GAGTTATTTTCACTG | 9873 |
rs185232170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019058 | AAAATGTGATATAAG[C/T]ACCCAAATGAGGAAA | 9873 |
rs185242099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002092 | TGTGGGAAATCCATA[C/T]CGATTTTCAACCACA | 9873 |
rs185244449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126978 | GGGAGGCAGAGGTTG[C/T]AGTGAGCCGAGATTG | 9873 |
rs185253195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095575 | TGGACATATAAGGGA[A/G]TGATATGCTATAAGG | 9873 |
rs185260595 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914000 | TAAAAATGGCCATAC[C/T]GCCTTAAGCTATTTA | 9873 |
rs185261136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056417 | TACCCCCAAAATGTA[A/C]TCTTTTTAAAAATTA | 9873 |
rs185262735 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074177 | CTAATGTGCCACAAA[A/G]TATCACTTCAATACA | 9873 |
rs185280509 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865685 | TTTCTTCCCTATTCT[C/T]CTAGCTGATATTGAG | 9873 |
rs185284915 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881699 | AATACTATTCAGTCA[C/T]AAAAAAGAATGAAAT | 9873 |
rs185288665 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904141 | GAGATGAGGTGAGGA[C/G]TTGTCAGAATATGGT | 9873 |
rs185308055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846702 | GACAACCAGAGCTCC[A/G]TTTCCACCAGTATCT | 9873 |
rs185319571 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968709 | TTGGCAGGGTTAAAG[C/G]CTATAAACTATATAC | 9873 |
rs185339880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926428 | GCTAATAGCTGGAGA[C/T]GATGGGATGGCCAGC | 9873 |
rs185345917 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947051 | CCAGGTGAGATTCAG[A/C/G]TCCAAGAAAATGAGA | 9873 |
rs185346335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138744 | TCCTGAGTAGCTAGG[A/G]CTACAGGCGCACGCC | 9873 |
rs185359870 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894179 | GGTTGTTAGGCCAAT[A/G]GCATAACATTCTAGT | 9873 |
rs185369923 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972080 | AAGAGTTAATCTCTT[C/T]AAAATTTTCTTCTTA | 9873 |
rs185375011 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890274 | GCAAAGAAGAAAATG[C/T]ATTCATGCCAACCTA | 9873 |
rs185376843 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939763 | AGCTGGGATTACAGA[C/T]GCCCACCAAGACACT | 9873 |
rs185377466 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910666 | TCCCTAATCTCAAGT[A/G]CCCAGGGATACAAAC | 9873 |
rs185384171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930364 | GTTCTTTGTACATAC[C/T]GAAGATCACCCAATC | 9873 |
rs185398608 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869185 | GTGCTGGGATTACAG[C/G]CATGAGCCACCTCAC | 9873 |
rs185403435 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875365 | CTATCTATCTATCTA[G/T]CTAGCTATTATTTAT | 9873 |
rs185405508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854777 | CAGAATGGTGATTGT[C/T]AGAGGCTGCATGATG | 9873 |
rs185411176 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906904 | ATTGTCTTGGCTATG[C/T]GGGCTCTTTTTCGGT | 9873 |
rs185461789 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078823 | TCCTGGACTCACGTG[A/G]TTCTCCTGCTTCAGT | 9873 |
rs185463215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086044 | AAGAAAACTATGTGC[A/G]GGCAAAATGTAAATA | 9873 |
rs185471573 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051589 | GAAATAAAGACCAAC[A/G]ACTTTATACTATTTT | 9873 |
rs185475769 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120729 | AGCAAAATTGTGTCT[A/T]AAAAAATAATAATAA | 9873 |
rs185484148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130790 | CATAATATGGAAGTA[C/T]ATATTTACATTTAAA | 9873 |
rs185494271 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920836 | AAAACAGATACATGA[C/T]AGGACTTCAAAGCAC | 9873 |
rs185517797 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962334 | ACTTGGGCATTCTTG[C/T]GTCTCTAAATTTTCT | 9873 |
rs185521083 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884028 | GTGACTAGCACTTGG[C/T]AATTGCAAAGAGGAA | 9873 |
rs185540483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012840 | AACAAATTTGACAAA[C/G]ACAAAAAACAAAACT | 9873 |
rs185560266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849637 | CTGTTATGTTGCCCC[A/G]ATATTAACCTAATAA | 9873 |
rs185591246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067007 | CCAAAGGATTATAAA[C/T]CATTCTACTATAAAG | 9873 |
rs185599085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136921 | TGGTGGCAGCTACTA[C/G]GGAGGCTGAGGCAGG | 9873 |
rs185602991 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861950 | AAAAAAAAAAAAAAA[A/G]ATAATATATCATTAC | 9873 |
rs185610794 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028569 | TGGGATAATGTTGGC[A/G]TGAGTTAAGACTTTG | 9873 |
rs185612500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010332 | GTACTGTTTTTCAGA[A/T]TTTTCTTGTATCTCA | 9873 |
rs185622050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991536 | GTGGGCTTCATCCCC[A/G]GGATGCAAGGCTGGT | 9873 |
rs185632386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064973 | AACTATTCCAAACAA[C/T]AGAAAAAGAGGGAAT | 9873 |
rs185646571 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072452 | TTTAATGAAGTTTTT[A/T]AAAACTTAAAAATCA | 9873 |
rs185654100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047171 | TACCAAACATGACTG[C/T]AAATTTGAAAAAAAA | 9873 |
rs185663457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031044 | TAAAAAAAAGGGAGA[C/T]CCTGCTATTTGTCAC | 9873 |
rs185668357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948171 | TGCCACCAGACCTGG[C/T]AAATTTTTGTATTTT | 9873 |
rs185681239 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969193 | AAAATCAGTGTTAAC[A/C]GTCTACCTACTCCCT | 9873 |
rs185682464 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033262 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGCGAG | 9873 |
rs185689078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968143 | TATAAGGCCTTTGGA[A/G]TTATCTTGAGGTTTT | 9873 |
rs185722185 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001664 | TTATATAAACTGACG[C/T]GGCTGGAAAAATATA | 9873 |
rs185730415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980786 | TATACATCTCACTCT[C/G]TTCTACCATATTGAG | 9873 |
rs185741147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864230 | GCAATAAAAGAACAG[A/G]GTGGGCATAGTGGCT | 9873 |
rs185746541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958734 | GTTTTATCTATAGTC[A/C]CTTAAAAGTAATCAG | 9873 |
rs185755875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080077 | GCTGAGACAGGAGAA[C/T]TACTTGAACCCAGGA | 9873 |
rs185767575 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018529 | TGTCTTTTTTTTTTT[C/T]TTTTAATCATTATAT | 9873 |
rs185773315 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042029 | CTTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTTG | 9873 |
rs185777114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109112 | CTGTTTTTATGCCAG[C/T]ACCATGCTGTTTTGT | 9873 |
rs185798316 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887312 | ATGTACTGCCTTCCA[A/C]AGAGCAGGTACTCAA | 9873 |
rs185813870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952570 | CCTCAAGTGATCTAC[C/T]GGCCTCGGCCTCTCA | 9873 |
rs185815472 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908814 | TATGCCACTATGCCC[C/T]GCTATAGTTTTGTAC | 9873 |
rs185816183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989915 | CAGCAAAGCAGGAGG[A/G]GACACTGGTGAAGGA | 9873 |
rs185819478 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016434 | TGTCTCCATTTTTAG[C/G]AAAAGGGTGAGTATA | 9873 |
rs185820432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922769 | TCTTGCCAATCAGTA[A/G]AGGTAAAAATTGAGG | 9873 |
rs185824047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974270 | AGCAGAAGAGCAACA[A/G]AACACAAGAGGGAAA | 9873 |
rs185847604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006709 | GCTTACTGCTCTTAC[C/T]GCCAATTGGCATATA | 9873 |
rs185865193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844866 | AAAATCCAGATTCTG[A/G]ATGTTGCCATAGCTC | 9873 |
rs185868512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005175 | AAAAATCTCCATCAA[A/G]CCTCCATTTCTCACC | 9873 |
rs185879396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985454 | AGACTATTCTCAGTA[C/T]CATACAACTTCATAC | 9873 |
rs185886891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964639 | CAGCAGAATCTTCTG[C/T]GTTAACTTCCGAATC | 9873 |
rs185893609 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131314 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 9873 |
rs185907639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060898 | TGAAACCAGGCACTA[C/T]AGTGAGATTCCCGTG | 9873 |
rs185907791 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837460 | AATTTGATTTCTTAA[A/C]CAAGGAAAAAAAAAA | 9873 |
rs185914978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907739 | GGGACTACAGGCACC[C/T]GCCACCACGCCTGGC | 9873 |
rs185923414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878190 | AGGCTGAGGCAGGAG[A/G]ATCATTTGAGTCCAG | 9873 |
rs185923904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106387 | CTCCACCCTGGGTGA[C/G]AGAATGAGACTCTGT | 9873 |
rs185924623 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099610 | TACAACCGAGTATTA[A/C/T]CCAGTCACAAATGCA | 9873 |
rs185925219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861560 | TGTAACAAAACCAGA[A/C]AAGAATACTACAAGG | 9873 |
rs185930775 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128171 | CTGACATACTTAATT[C/T]AAAAGGAATTGGGAA | 9873 |
rs185931366 | snp | A/C | | | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72921940 | TGATCATACACATTT[A/C]CATCAAGAGCCTGTA | 9873 |
rs185937131 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084439 | TCTGTTGCCTAGGCT[C/T]GAGTGCGGCGGTGAG | 9873 |
rs185937757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941474 | TAAAATATAGACTCC[C/T]AACTCTATTAATATA | 9873 |
rs185938043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987321 | TCATTTATCATTAGG[C/T]AAAATTAACCTCTAT | 9873 |
rs185939617 | snp | A/C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896277 | AGGTAAAGGGGAAAG[A/C/T]GTATTCTCATTCCGA | 9873 |
rs185960628 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842466 | ACTGACTGACAAGTC[A/T]CTGGTTTCCCAAATG | 9873 |
rs185964058 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959206 | TTTCTTTTCCACTTC[A/T]TATATCCAGCAGTCT | 9873 |
rs185970980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023956 | TCTGGGAAAGACCAA[C/T]TGATAGAGAAAACAG | 9873 |
rs185981405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027966 | TGGAAACCTCTGCCT[A/G]GATTTCAGAGAATGT | 9873 |
rs186002943 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990747 | ACTAAATGCCCACAA[A/C/G]AGAAAGCAGGAAAGA | 9873 |
rs186118724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981634 | GTAAATGTGTTCTTT[A/G]AAACTGTTGGTCCTT | 9873 |
rs186122986 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064235 | GATGTTCTTTGAAAC[C/G]AATGAGAACAAAGAC | 9873 |
rs186126968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009867 | ATAGTTTGACTATAA[C/T]GTACCATGGAGAATG | 9873 |
rs186133124 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938451 | GATAGTTAAGGGTGT[A/T]CAAAGCAGTAGCCGG | 9873 |
rs186146076 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104183 | ATTAGTGAGAAACAC[G/T]ATGTACACTGCAACT | 9873 |
rs186160830 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040943 | CATGACAGCAACTTT[C/G/T]TTAGCTCCCACATAT | 9873 |
rs186167142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997670 | AAAAATCCTGGAACT[C/G]AAAAGTACATTAAGA | 9873 |
rs186173498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023409 | TCATCAAAGAAGATA[C/T]AAGAATGGCAAACAA | 9873 |
rs186186758 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079316 | ATTCTCCTGCCTCAG[A/C]CTCCTGAGTAGCTGG | 9873 |
rs186190641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099041 | CCACATAGTAAGACA[C/T]CATCTCTACAAAATA | 9873 |
rs186199066 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059124 | TACTTTCAGTGAGAA[C/T]GCACACTATAATTCA | 9873 |
rs186204721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014883 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 9873 |
rs186244449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082682 | CCATGTAGAAAATTT[A/G]CTGTATGTTAATTTT | 9873 |
rs186249879 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068907 | GTAGTCCCAGCTACT[G/T]GGGAGGCTGAGGTAG | 9873 |
rs186255263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046434 | GAATACCAATTTTCA[C/T]AGAAAGGAAACAAAA | 9873 |
rs186255333 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055593 | TTCATTAAGATTTTA[C/T]GCATATTTTATAATG | 9873 |
rs186267882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110166 | TTTTTTTTTTTGATG[C/T]GTCTTTGGTCTTTGG | 9873 |
rs186277858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131981 | AGTCACTGACATCCA[C/T]ATATTTCCACAAATT | 9873 |
rs186283532 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086479 | TACAACTTAAGGAAC[C/T]AGAAAAAGAACAAAT | 9873 |
rs186286239 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083544 | CAAAGCGAGACTCCA[C/T]CTCAGAAAAAAAGAA | 9873 |
rs186314162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860305 | ACATTTATAGAACAT[A/G]ACCCCTAACAATAGC | 9873 |
rs186315057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855916 | CTATTAGAATATGCA[C/T]GTTTTACTTTTTAAA | 9873 |
rs186330048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017834 | TAAACAATCACAAAT[A/G]TATATAGGAAAATGT | 9873 |
rs186333490 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875804 | CTTTGGCTAGTGGGG[A/C]ATTTGCCAATTTAAT | 9873 |
rs186336835 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121004 | TTGTTTAGACAAGAG[C/G]CAGAGAGCTACTAGT | 9873 |
rs186337358 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936922 | GTAAGTCCAATGTAT[A/G]GACTTCCTTGGAGAC | 9873 |
rs186340632 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979606 | GACTCCAATGTTTCA[A/G]TGAAAGAGTTTTCAA | 9873 |
rs186341497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139007 | TCAGTCAGAAAACAA[C/T]AATCTTGATATATCC | 9873 |
rs186347933 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910946 | CCATTCTGTGGGTTG[C/T]TGCTTCACTTTGTTG | 9873 |
rs186376600 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905041 | TTTACAAACAGCTGT[A/C]GTGGGCTGAATGGTA | 9873 |
rs186382560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918119 | CCTTTAACTCCTTTG[C/G]TTAAGTTTATTCCTA | 9873 |
rs186386691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937533 | ATATGGGACCATTAA[C/T]GGAAAGGCAAGGTCT | 9873 |
rs186399419 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127395 | TCCATAAATTACTCC[C/T]GATCAACACTGACAG | 9873 |
rs186425937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035358 | TTTTTTGTAGAGACG[A/G]GGGTCTCATCATGTT | 9873 |
rs186465880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053858 | ATTGTTTTCTTTTTC[C/T]CTATGTATGACCATT | 9873 |
rs186467771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927432 | TCATCAATTGCAACA[A/G]ATGTGCCACTCTGAT | 9873 |
rs186468882 | snp | A/G | 0.00205798 | 0.0320118 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989100 | ACTGGTCCACACACT[A/G]TAAAATACAAAAGTA | 9873 |
rs186469440 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032914 | ACAGGAAATCAAGCT[C/T]GCGAGCAGTGCAGTG | 9873 |
rs186477637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932649 | TCTCTTCACTTAATC[A/G]TCTACTTGGATATCT | 9873 |
rs186485521 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088861 | TTTCACAAAAGATAA[A/C]AGGAAATATTTAAAT | 9873 |
rs186498849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895911 | ACAACGCTATATGCA[A/G]TACAAAATTTCTACA | 9873 |
rs186507265 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885246 | ACCAAGTGAGATTAT[A/T]TTATGCTAACAGTAA | 9873 |
rs186514264 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860815 | AGAGCAAGACTCTGT[C/T]TGAAAAAAAAAAAAA | 9873 |
rs186520050 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070381 | TAGAACCTAGCATCA[C/T]GCCAGTCGTAAAGTA | 9873 |
rs186525797 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000851 | TGAGAACATGTTGAA[A/G]TCAGAAAATCCTAGT | 9873 |
rs186542221 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891839 | GTAGGTTATAATGAG[A/G]TCATATTTTAAACAT | 9873 |
rs186543732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118200 | GGCAGGTGCATATAA[C/T]CCCAGCAACTTGGGA | 9873 |
rs186547003 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073748 | GGCCATAATGCCATA[A/T]AAGTGGCTTTGAAGA | 9873 |
rs186552347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957857 | GTGAGGGAGAGGGAA[C/G]AAACAGAACAAAATG | 9873 |
rs186553136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998327 | GGCAGATCACTTGAG[G/T]TCAGGAGTTCAGGAC | 9873 |
rs186558808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854495 | GGAGTGCAATGGTGC[A/G]ATCATAGCTCATTGC | 9873 |
rs186563679 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957019 | TCAAAGGACTCTAGT[C/T]TTTTTTTTTTTTTCT | 9873 |
rs186564718 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874591 | ATGCAAGTCATTTAA[C/T]TGCTGAAGCAGAAAA | 9873 |
rs186608120 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033304 | AAAAAAAAAAAAAAG[A/T]AGTTAGACTACAGTC | 9873 |
rs186623151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112367 | CTGCTGGACATATTG[A/G]AGCTCCATTATGTGT | 9873 |
rs186625206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104909 | AAATGGTGAAAATCT[A/G]TATTTTACAATATAG | 9873 |
rs186632988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036381 | ATATTTCACAACGTT[A/G]TATCGGTCTTTGGAG | 9873 |
rs186657825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913162 | TGATTTAATTACCTC[C/T]CACTGGCCCCTCCTC | 9873 |
rs186665447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929538 | TCAAAGCACGGGAAG[C/T]GGATGATAACCCTAT | 9873 |
rs186678424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949398 | GAGGTTACAGTGAGC[C/T]GAGATCATGCCACTG | 9873 |
rs186686917 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036324 | ATAGGAAATAAAAGA[A/C]AAAAAAAAAAAACCC | 9873 |
rs186692169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876859 | TTATTATTATATATA[C/T]GTCCAGGATTTTAAT | 9873 |
rs186694868 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893504 | GATTTTTAGTAGAGA[C/T]GAGATCTCACTATGT | 9873 |
rs186698111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878096 | ATAAATAAATGTAAA[A/G]TCAAAGAAATCAAAT | 9873 |
rs186712321 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914592 | AGACCGCACACCTAA[A/G]ACCACCTGATCTTCA | 9873 |
rs186734312 | snp | A/C/G | 0.00057876 | 0.0170032 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840850 | AAGAACTATGCATTC[A/C/G]ATAATCCTGCAAGAT | 9873 |
rs186768935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092453 | CCCGGCATCTTCTAA[C/T]ATAGCATCTGCTTTA | 9873 |
rs186775977 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143204 | GAGGCCCCCGTTTCA[C/G]AGACGGGGAGGCAAG | 9873 |
rs186781004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914857 | AGATGCCAAAAGCAA[C/T]TGCAACAAAAGCAAA | 9873 |
rs186791855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993868 | CATATGTAACTAACC[C/T]GCACGTTGTGCACAT | 9873 |
rs186792195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996151 | ATAAACCTGTTTCAA[C/T]ATTAAGCTTTGTTTT | 9873 |
rs186797187 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134483 | TCAAAAAAAAAAAGT[C/T]TCAGAACATCCATAA | 9873 |
rs186800750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952623 | AGCCACCATGCCTGG[C/T]CTATAGTTAATTTTG | 9873 |
rs186802032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970347 | TACTTACAATTCTAA[C/T]GTATGAAAATTGTCT | 9873 |
rs186840540 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965085 | TGAGCCACCGCGCCT[A/G]GCCAATCATTTTACT | 9873 |
rs186851236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847818 | CTGCCTCAGCCTCCC[C/T]AGTAGCTGAGATTAC | 9873 |
rs186853803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055858 | AGATTCAGGGGCTGT[A/G]GGAGGAGACAAAGGG | 9873 |
rs186854312 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850545 | TTTTTAGTAGAGATG[C/G]GGTTTCACTGTGTTA | 9873 |
rs186867395 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885931 | GAGGTGGGGTTACTG[A/G]GGTTTCTCCAGCCCA | 9873 |
rs186890603 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140517 | GCAGAGTGTGGATGG[A/G]GGCTGGGAGCCTAAG | 9873 |
rs186891434 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057991 | TTCACGCCATCCTCC[C/T]GCCTCAGCTTCCCGA | 9873 |
rs186904033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039335 | CCAGCCTAGACAAAA[C/T]GGTGAAATCCCATCT | 9873 |
rs186918483 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120398 | TGTCTCATTTGGTAG[C/T]AAACATTTCTTCAGT | 9873 |
rs186929867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076834 | TGTTATGCTAGGCCC[A/G]GCGCAGTGCCTCACG | 9873 |
rs186931990 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097665 | TCCCTTCACTTGTTA[C/T]TGAGAATTTCTATTT | 9873 |
rs186942910 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994387 | CTCTATGAAAAAGGT[A/G]GTAGTAGTAGTAGCA | 9873 |
rs186948625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971871 | TGGTGATTTGTTACA[C/T]AGCAACGGAAATCAA | 9873 |
rs186953128 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032109 | GAAAAATGAATAGCA[C/T]GGTCCTATTTTAATT | 9873 |
rs186999450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014703 | CCCTGGATTCTCTGC[C/T]ATTGTTTGAAGGGTA | 9873 |
rs187001445 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870328 | TGATATAATTGGGGG[C/T]TCCTTTAAGACTCGA | 9873 |
rs187002736 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933527 | TACTTTGAGTTGGGT[A/C]ATTGTTATTTGCAAT | 9873 |
rs187003149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839650 | AGTAGGATGGGGGTT[C/G]CATTTACCAAGATAG | 9873 |
rs187006338 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890060 | CAAAACATGAGGCAC[C/G]CTCCACTACTGCTGG | 9873 |
rs187014051 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974809 | AGAAAGAGGGCATTA[A/T]AAAAAAAAGGATATA | 9873 |
rs187047564 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869747 | GTCTGTTTCCTTTTC[C/T]TGTTCATAATGCTAT | 9873 |
rs187068617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030197 | CTTAGTTCCTATGTA[C/T]ATGTATGCGTGTGTG | 9873 |
rs187070125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051204 | ATGGTGCTGCCAGTG[C/G]TGTTGCATGCTGAGG | 9873 |
rs187071463 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096500 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCTGCTGC | 9873 |
rs187073173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123435 | CAAATGAGAATCATA[C/T]GCTATGGCTTTTTAT | 9873 |
rs187080392 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011928 | TCTTCTTAGTGGAGG[A/C]GGTACGAAGTGCCCC | 9873 |
rs187084501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085315 | CAGCTTAGTAAACAC[C/G]AGGAATCTGACTCCC | 9873 |
rs187092924 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066513 | TCTAATTAAACTAAA[A/G]AGCTTTTGCACAGCA | 9873 |
rs187095780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938603 | CACAGCATCTCACCA[A/G]ATGGAGAAGCTTAGG | 9873 |
rs187097506 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136198 | GAAAAAAGAAGGGAC[A/G]TAATGGGGAAGAACT | 9873 |
rs187097697 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118984 | CTAATAAATAAATAA[A/T]TAATTTTTGTTTGAA | 9873 |
rs187118784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883220 | AGAAAAGCTTGAACT[A/G]TAACACTTCTAGAAG | 9873 |
rs187122703 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905924 | GTGTCTTTATAGCAG[A/C]ATGATTTATAATCCT | 9873 |
rs187127477 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052416 | TATAATTTTTTTTTT[A/T]AAAAAAGACACCTGT | 9873 |
rs187129479 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919276 | GGGCACTACATTATT[A/C]TTATTAAATTTTTAT | 9873 |
rs187130587 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053025 | CTAATTTTTGTATTT[G/T]TAGTAAGATGGGGTT | 9873 |
rs187137294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848723 | CAGAGGGAATGTTGA[A/G]TGAATGTGAACTGTT | 9873 |
rs187143815 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867778 | ATTATCTTTTTAAAA[A/G]ATTTTGGCTATTATT | 9873 |
rs187159861 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949999 | TGGCTGTTCCATTTT[A/T]CATTCTCACCCAATT | 9873 |
rs187165736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986120 | ATGAACACATATGCA[A/G]CCCAACTACTTCCCC | 9873 |
rs187171619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908371 | TCTCTTTGATATATT[G/T]ATTTCCTTTCTTTTG | 9873 |
rs187276589 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088307 | AGGTTTGTAGCCTAG[A/G]AGCAATAGGCTATAT | 9873 |
rs187290288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005567 | ACTGGAGTGCCCTCA[A/T]GTCAGACCCCAGGCT | 9873 |
rs187304287 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870774 | GCGTGGTGGCGGGTG[C/T]CTGTAGTCCCAGCTA | 9873 |
rs187307526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132272 | TGGACTTCAATTTTC[A/C]ACTAATAACAGTAGC | 9873 |
rs187308356 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851686 | AGGCAGAGGTTGCAG[C/T]GAGCCGAGATTGTGC | 9873 |
rs187331563 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032577 | AAATGTTTATTACCT[G/T]CCTAACTGAAAAAAA | 9873 |
rs187348808 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866086 | CTAGCTGAAGGAAAA[A/T]CATGGGTTTGATTGG | 9873 |
rs187348829 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889321 | TATTAATTCAACATA[A/T]GTCTCTTCCCCTGCC | 9873 |
rs187349271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020672 | TGATTATGTAAGATT[A/T]AAAAAACAGTATATT | 9873 |
rs187360828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925685 | TCCACCAGTAGACAC[A/G]ATTATCGAAATGGCT | 9873 |
rs187361149 | snp | G/T | 0.00504829 | 0.0499866 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867845 | AATCAACTTGTCATA[G/T]CCAAGAAAAGAAATC | 9873 |
rs187367473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002914 | TCTCACTATAGTGAA[A/G]GCTCCATGAAGGCAG | 9873 |
rs187370322 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886656 | ATAAAAGTGTGTGCA[C/T]AGGTCCTCCATAAAC | 9873 |
rs187371368 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047652 | CAAATATTTATGCTC[C/T]TTCTTTCAGAAATGG | 9873 |
rs187374852 | snp | A/T | 0.0629771 | 0.165899 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983305 | TCTCAAAAAAAAAAA[A/T]AAATAAATAAAAGAA | 9873 |
rs187376805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964980 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 9873 |
rs187378103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922082 | TGGACAAAAGATACA[A/G]ATTGTAAGTAAATAT | 9873 |
rs187390428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038651 | AGCTAAACATTGAAT[A/G]CAAATGGACATAAAC | 9873 |
rs187394491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920510 | CTTTGAGAGGCAAGG[C/T]GGGTGGACCACTTGA | 9873 |
rs187398822 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939317 | ATTGTAACTAAGCAT[A/T]TTTCCCCCAGTCGGT | 9873 |
rs187401962 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861396 | TATTTAAAAACTTCC[A/C]AAAAAAAAAAAAAAC | 9873 |
rs187414999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961896 | ATTTCAACTCGATGT[A/G]TAAATGCCACATTTC | 9873 |
rs187433664 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008832 | CTACTTAACATTTCA[A/G]ATATGAAGAGATCTA | 9873 |
rs187456826 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044710 | TGGGTAAATACTATA[G/T]AGAAAACAGTGCACA | 9873 |
rs187460323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111641 | ACTCCTGTTATTTTA[C/T]TTTTGGGTGTGTGGT | 9873 |
rs187466666 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069981 | AAGACCAGGTAGAAA[C/G]TTAGAATGCACATAC | 9873 |
rs187471323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090282 | CCAGGCTGGAGTGCA[A/G]TGGCGGGATCTCGGC | 9873 |
rs187481930 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133624 | GAGATGGCAAAACCC[C/T]ATCTCTACTAAAAAT | 9873 |
rs187491604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112744 | ACCTCTGCCTCCCAA[A/G]TTCAAGCAATTCTCC | 9873 |
rs187499384 | snp | A/G | 0.000121751 | 0.00780132 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900290 | CAGAGCACTGACAGG[A/G]GAGAGCTCAATATCC | 9873 |
rs187507922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975863 | TATTAAGAATTACTA[A/G]GCTTTTAAAAAATCT | 9873 |
rs187516175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923519 | ATTAGTGATTAGGAA[C/T]GGTATATCTTTGTAG | 9873 |
rs187517451 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934601 | GGCCTCCCAAAGTGC[C/T]GGGATCACAGGCATG | 9873 |
rs187519009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879955 | CGTGAGCCGAGATCG[C/T]GCCATCGCATTCCAG | 9873 |
rs187523959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900721 | AGGTTGTAATATAGA[A/G]GGAAATGCTGATTTC | 9873 |
rs187525312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943801 | TATTAGTTCATTAAC[A/T]ACAAGAAGTTTCAGT | 9873 |
rs187526925 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916041 | TGGGAACAACGCACA[C/G]TAGGGCCTACCAGAG | 9873 |
rs187551304 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864170 | GAAAGTGGCTGAAAA[C/T]GGGGAAGTGATGTTA | 9873 |
rs187566279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124554 | AGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 9873 |
rs187574150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081504 | ATTTTGTATTAAAAA[A/T]TTTTAAAGCATATCA | 9873 |
rs187577629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946088 | GCTGCTATAAAGACA[C/T]ATGCATACATATGTT | 9873 |
rs187591670 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021233 | AGATCAAACATAGAA[A/T]AAAAAAAAAAAAAAA | 9873 |
rs187609457 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847148 | ACGATAGGCATGTGC[C/T]ACCATGCTCAGCTAA | 9873 |
rs187614168 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882120 | ACTGCACTCCAGCCT[A/G]GGTGACAGCAAGACT | 9873 |
rs187625691 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856958 | ACAAAAATCAAAACA[A/C]AACACAACACCCATA | 9873 |
rs187625768 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918799 | TTATTAATTGGAAGG[C/T]ATTTCCTTATGGAGA | 9873 |
rs187642145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024365 | AGCTAGAAACTGTAC[A/G]ACTAAAGACAAAAAA | 9873 |
rs187652822 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007281 | AATATCATATAAGAT[A/G]TCTAGGAAAACCTAG | 9873 |
rs187656472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882591 | GTGATAGATATCTTA[A/G]TTACTCTAATTTGAT | 9873 |
rs187660527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988033 | AGCCCTTGATAAACC[A/G]CGGAGCCCCTGAATT | 9873 |
rs187669352 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061657 | ATTGCTGAGGCTTGA[A/G]TAGGGTGGTTTTATG | 9873 |
rs187682335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975066 | AGAAAAACCGAAAAA[A/G]AACTTGGCTTTCTGT | 9873 |
rs187682577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042268 | CAGGGGTCATTCTTC[C/T]GCATATGGATATTCA | 9873 |
rs187683215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106639 | AGTAACATAACATTT[C/T]CATAAAAAATGGACC | 9873 |
rs187693854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953223 | GAGAAAGCATGACAA[A/G]CATTAGAAACTAAGG | 9873 |
rs187695250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066052 | GCATTGCCAAAACAA[A/T]CCTGGGCAAGAAGAA | 9873 |
rs187708399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062655 | CATACACCGTTTCAA[C/T]AGCCAAATCGATCAA | 9873 |
rs187714139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872868 | TCTGGGGAAATACTA[A/G]ACTGTTTTTCAACGT | 9873 |
rs187726818 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026619 | CTTAATTGAGAACTA[C/T]ATATGATTAAAGATC | 9873 |
rs187728151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915320 | AAATTAGTTCAACCA[A/T]CGTGGAAGACAGGGT | 9873 |
rs187733491 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933883 | GGAGGCTTAGGTGGG[C/T]GTATCACTTGAGCCC | 9873 |
rs187734740 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953412 | ATAAATTCTCTCTCT[C/T]AAGGCCAGTTGAGAG | 9873 |
rs187750074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878501 | CTTGGAGAAACAGCT[A/G]ATTCTAAGTCTGGGC | 9873 |
rs187751465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137015 | CCTAGCCAACAGAGC[A/G]AGACTTTGTCTCAAA | 9873 |
rs187752211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852219 | TTAAAAAGTCAAAAA[A/G]TAACAGATGCTGGTG | 9873 |
rs187753457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898881 | ACTACAGGTGTGTGC[C/T]ACCATGCCCAGCTAG | 9873 |
rs187761486 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915779 | GCCGAGATCACGCCA[C/T]TGCTCTCCAGCCTGG | 9873 |
rs187774352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029354 | AAGATCGGTTTGATG[C/T]AATTATTTTAGAATT | 9873 |
rs187823181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102954 | ACAACATGGATGAAT[A/C]TCAAAAACATTACAC | 9873 |
rs187839590 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133161 | ACCCATCATGTATTA[C/T]TGCTGGTGGGAATAT | 9873 |
rs187856959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876609 | TGGTCTTGTTGAATG[C/T]TCTATGTGTACTTTA | 9873 |
rs187867615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892585 | TAGTATAGATAATTA[C/T]GTTTTTGTGTTTTTG | 9873 |
rs187886663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949476 | AAGAAAAGAAAAGAA[A/G]GGAAAGAAAAAGAAA | 9873 |
rs187886815 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982772 | TCTTTTGTTTGTCCC[A/G]TACGCAGCTCAAAAT | 9873 |
rs187892739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965554 | TTTTTTTAAAACTCA[A/G]TATTTTCATGTATTT | 9873 |
rs187896894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856407 | AAAACTGACTCTCCT[C/T]TTAACCACTGTTTGC | 9873 |
rs187901758 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905513 | TTACACAGGTATACA[C/T]GTGCCATGCTGGTTT | 9873 |
rs187904527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141417 | TAGAAACAAATCCCC[A/C]GCAAATTTGCAAACG | 9873 |
rs187911426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019742 | TTACAGTAAAGGTCC[C/T]AAATAATATTGCACA | 9873 |
rs187913161 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913812 | TGATATACAAAAAAA[A/C]CAAAAAAAACCCAAA | 9873 |
rs187938207 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867166 | GAGAGTAATGGGTGG[G/T]GAGGTGACAGTAGGA | 9873 |
rs187943531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062116 | TTCAGAGGAAAGATC[A/G]GCAGCAATCTTTGAT | 9873 |
rs187960053 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043345 | ATTATCAGTTTCCAT[A/T]AGCAAGTATTTATCA | 9873 |
rs187971549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967774 | TATGGTATGTGAATT[A/C]TATCTAATTTTTTTT | 9873 |
rs187975062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124139 | GCTGGAAACCATCAC[A/T]CTGAGCAAACTATTG | 9873 |
rs187986293 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084860 | GACAATTTACCTTGA[A/C]TATCCTGAGTTTAAA | 9873 |
rs187986695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081154 | TTAAAACTTTAAATC[A/G]ACCAGGCACTGTGGC | 9873 |
rs187990704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102179 | TAAAATGAGATACCA[C/T]TGAACACCCACTAGA | 9873 |
rs187999986 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129979 | TGCCTCCCGGGTTCA[C/T]GTCATTCTCCTGCCT | 9873 |
rs188003127 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909334 | AGTCTCGCTCACTCA[A/G]TGCTCAATGTTGCCC | 9873 |
rs188005617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129742 | CCCCTGACCCCACCC[A/G]CAGTCCATGGGAAAA | 9873 |
rs188013226 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924553 | TCCCAAAGTGCTGGG[A/T]TTACAGACATGAGCC | 9873 |
rs188019894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011687 | TATCTTAGTTTCAAG[G/T]CCCAGGAAGGTTGAA | 9873 |
rs188033301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873278 | AGGCTGCAGTGAACC[A/G]AGATCGCGCCACTGC | 9873 |
rs188035366 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853500 | ACTCACTGCAACCTC[C/T]GCCTGCCAGGTTCAA | 9873 |
rs188041954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048516 | ATGAATCTGCAGGTT[A/G]GCTAGAGCATCTCTG | 9873 |
rs188051439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846423 | CTGACCTCGCGATTC[A/G]CCCGCCTTGGCCCCG | 9873 |
rs188053410 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888931 | CCAGCCAAACATATA[C/T]TTTCATGAAATCTAT | 9873 |
rs188053870 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056859 | AGGCCAAGGTGGGTG[C/G]ATCACAGGGTCAGGA | 9873 |
rs188084098 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863288 | AAGGACAGTTAAAAA[A/C]AAAAGTTCAAAAAAG | 9873 |
rs188115229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017364 | AGAAATCATTAACAT[G/T]GAGATACTTATTTCT | 9873 |
rs188165197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869264 | AAAAAAGGAAATCAA[A/G]GCTTTTTTCCCTCAA | 9873 |
rs188194080 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038500 | TGGTACATATACAGC[A/G]TGGATACTATGCAGC | 9873 |
rs188194861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850249 | TTTGTATTTTTAGTA[A/G]AGATGGGGTTTCACC | 9873 |
rs188201864 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960649 | GCCATTCCCATTCCT[C/T]TAAAGTTACAAAGAT | 9873 |
rs188209915 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002748 | CTTCCAGTCTCAGTT[G/T]AAATGTAACTTCCTT | 9873 |
rs188210123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929987 | TGTAAGAGGGAAAGC[A/G]CCAAAGAAACATTTT | 9873 |
rs188211141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075247 | GAAAACCATTTCATG[A/G]TATTTCCTAAAGCTG | 9873 |
rs188214918 | snp | C/T | 0.201418 | 0.245234 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962601 | TGAACTAAATTCCCC[C/T]TTTTTTTTTTAAACT | 9873 |
rs188242564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055132 | CTTATAAAAACCATC[A/C]GATCTCGAAAGAACT | 9873 |
rs188244083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071764 | GAAATGGACAGAGTG[A/C]AACACAGGTTTCTTG | 9873 |
rs188253689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010576 | GATAGATCTATGGTG[C/T]TGTTTGGTAGGGCCC | 9873 |
rs188262611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034536 | ATAGAGATCAAAGTT[G/T]CCACTCTTGTGAAAA | 9873 |
rs188263615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928059 | AAGGTAAAGGATGTG[A/G]TATAATGTTAGTCTT | 9873 |
rs188263941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906683 | TTTATTAAACTGAAT[C/T]CTTTCCCCATTTCTT | 9873 |
rs188264695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115518 | TCTATACTTTCGTGT[C/T]GTTTTCATGTCTTCT | 9873 |
rs188273904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969457 | ACTGAGAGGGACAGA[A/G]ACAAAAAGATGAATC | 9873 |
rs188275736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134200 | TCAGCACCATGCACA[A/G]TGGCTCATGCCTGTA | 9873 |
rs188282848 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091694 | AGCAAATGTGGTCTT[C/T]TCCACTTGGAATTTC | 9873 |
rs188317584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074606 | AAAAGAAAAAAAATA[C/T]ATTTCCTTAAAATTA | 9873 |
rs188329649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120051 | AGGAAGATGCAAAAG[C/T]AGAAACCCCTGATAA | 9873 |
rs188349089 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107451 | TAATAATCACATTAG[A/C]GTAAATGGGGTATCC | 9873 |
rs188359255 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082386 | AAAGCATTCAACAGA[A/C]ATATTAAAACTGATG | 9873 |
rs188375631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843813 | AACACAGCGAGACCC[C/T]CATCTCTACCAATAA | 9873 |
rs188386442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879084 | CCACTGCACTCAAGC[C/T]TGTGCGACAGAGTGA | 9873 |
rs188389203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012865 | AAAACTCTGCCAAAT[C/G]ATTTGCAAGTCCTCT | 9873 |
rs188403376 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994836 | ATCTTAAAAGCTTTT[A/G/T]AAAAATTGACATATA | 9873 |
rs188410484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888131 | AAACAAGATAGCCAA[G/T]TATAGGAATCTGAGA | 9873 |
rs188436826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931728 | AGAGATCGCACCACT[A/G]CATTCTAGTCTGGGT | 9873 |
rs188443012 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951857 | GAGGAAATGAGGCTA[A/G]CGTTCAGTATAGCAG | 9873 |
rs188446950 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851966 | ATTGCAGTGTCAACC[C/T]CCTGGGCTCAAGCAA | 9873 |
rs188452241 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907348 | CTTGCCTGATTGCCT[C/T]AGCCAGAACTTCCAA | 9873 |
rs188457629 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021374 | ATGGAATACTATGCA[A/G]CCATAAAAAACAATG | 9873 |
rs188459369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973439 | TATATACAATGAAAT[A/G]CTATATAGCAAAGAT | 9873 |
rs188460456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921484 | TAGTACTCTTTGTAC[C/T]GACACATGACCTGTT | 9873 |
rs188461678 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895635 | CAGATCAGGAGAAAG[A/G]TGACTAAACCAGTAG | 9873 |
rs188464790 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941062 | ATTGGTGGTTCTTGC[C/T]GGGCAGCTTAGAGAA | 9873 |
rs188474062 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869503 | AAGAAAGGAATCAGG[G/T]TCTCCTAACAATGGA | 9873 |
rs188478537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914315 | TCAGGTGCCCAGCCT[G/T]CCCTAAGCAATTTAT | 9873 |
rs188481358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070749 | AAATTAAAAAAAAAA[A/G]AGAAATTGAACAAGT | 9873 |
rs188485147 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028919 | AGTTTCCTGAAGGCT[C/T]CCAAGCCACGTGAAA | 9873 |
rs188497795 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099924 | CCCGTCCCTATCCCC[C/T]ACTAATGAGGCCTTT | 9873 |
rs188507295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057539 | GACAGAAGGGAAGAA[A/G]AGAGGAAGGGAGGGA | 9873 |
rs188512724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850400 | ATTTTATTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 9873 |
rs188535705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117834 | ACCTTATTTTTGGTG[A/T]CTTTAAAGCAAATTG | 9873 |
rs188542700 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911610 | TATTTATTCTCCCAA[G/T]CCATCAACATGGAAT | 9873 |
rs188548999 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883825 | TATTCCCAGCTACTC[A/G]GGAGGCTGACATGGG | 9873 |
rs188552561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033063 | GGGGGCTGAGGCATG[C/T]GGATCATGAGGTCAG | 9873 |
rs188552972 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992298 | ACATTCCATGCTCAT[G/T]GGTAGAAAGAATCAA | 9873 |
rs188555206 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948619 | TTAACAAAATTTTAA[C/T]TTACCATTTTAATGG | 9873 |
rs188561646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954630 | TTGTCATTACTGAAA[C/T]TGGGAAGATCAAAAG | 9873 |
rs188562410 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134324 | AAAAATACAAAATTA[A/G]CCAGGCATGGTGGTG | 9873 |
rs188576890 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998895 | AATGATGCAGCTGCT[A/T]TGCAAAACAATTCTG | 9873 |
rs188595798 | snp | A/G | 0.000988419 | 0.0222088 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843416 | ACTCCTAAAAATGTC[A/G]CAAGAAAGGGCGATA | 9873 |
rs188616081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963347 | CTATCTCATTTAGAT[G/T]TCCTAAAGCAATCTG | 9873 |
rs188626890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136256 | TACAGTCTAATGTGC[C/T]GTAGATTTTTTTTTA | 9873 |
rs188627175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096657 | AAAAGGTGCATCCTT[A/G]TGTTCTTCCTGAACT | 9873 |
rs188686890 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068465 | CACAAAATTTACCTA[C/T]GTAACAAACCTGCAC | 9873 |
rs188692282 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872226 | TTTTTTTGGTAAAAC[G/T]TTATTGACATATAGC | 9873 |
rs188697008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052261 | CAATAAACATGATTT[C/G]AGTTTAAATTTTGTG | 9873 |
rs188697362 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031803 | AGGTAAGAGCTGGCA[C/T]AGCAGCCTTTTCGCC | 9873 |
rs188702916 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109311 | CTGTAGATTGCTATA[A/G/T]AAACTATGGACATTT | 9873 |
rs188706353 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908950 | TGAGCCATTGCATGT[G/T]GCCCTGTCTGCTATT | 9873 |
rs188707078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138130 | GAGCAACAGACTATA[C/T]CAACTTAGCTTAGAT | 9873 |
rs188710779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131674 | GCACCACTGCACTCC[C/G]GTCTAGGCAACAAAC | 9873 |
rs188717949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944159 | TCCTCAATAAAATAC[C/T]GGCAAACTGAATCGA | 9873 |
rs188718115 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988107 | AAACTGTATTAGAAA[C/G]ATAGCCCCCTCCTTA | 9873 |
rs188719078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086416 | CCATCTCAAAACAAA[C/T]AAACAAACAAAAAAC | 9873 |
rs188746994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909174 | GCTGAGTGTCTGGGA[C/T]TGCAGGCACACGCCG | 9873 |
rs188753750 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013191 | TCCACCACTCCAGTT[A/T]ACCTCTAACCCACAT | 9873 |
rs188769907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005205 | CAGCTGCCACCCTAA[C/T]GTCTGCTCTCTTTTA | 9873 |
rs188773854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054135 | ATTGTCTATGGCTGC[C/T]TACACTCTACAACAG | 9873 |
rs188776247 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985569 | GAAAGACTCTAACAA[C/T]AGGCTCTATGAAGTC | 9873 |
rs188786416 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964705 | CTTTATGGTAATAGC[C/T]TTACTGGTATTCTTG | 9873 |
rs188789967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090857 | TTGTACAACCACCAC[C/T]ACCTCTAATTTCAAA | 9873 |
rs188792690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942163 | TCCTCACAGTAATGA[C/G]AGCGTTCTCACTCTA | 9873 |
rs188813535 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977622 | TATGTGCTGCCGAAG[C/T]GAGCACGCTCTCACA | 9873 |
rs188833365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935709 | TGAATTTATCAGTTG[A/G]TATAAAGTAAAATCA | 9873 |
rs188839453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080832 | ACCTGTAATCCCAGC[A/T]ACTCAGGAAGCTGAG | 9873 |
rs188847554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025155 | ACATACCCAAAGGAA[C/T]ATAAATCATTCTATT | 9873 |
rs188849741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016290 | CCTGGGTGACAGAGT[A/G]AGGCTCTGTCTCAAA | 9873 |
rs188871989 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010924 | ACAGCAGTGGCAGTG[A/G]TGGGATAATCTTCTG | 9873 |
rs188894363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868801 | CTATCAGTCTTACAT[A/G]GCAAATATTCTCAAG | 9873 |
rs188900965 | snp | A/C/G | 0.00279242 | 0.0372774 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040894 | CAAACTGCTCCCCCC[A/C/G]CTCTTTGGTAACTAT | 9873 |
rs188902893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023204 | AAATTGGACCTTATC[A/G]GAATTAAACTCTTTC | 9873 |
rs188908941 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066828 | CATTAAAAAGTCAGG[A/G]AACAACAGATGCTGG | 9873 |
rs188925524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108376 | TTCACTTTGTTGATT[A/G]TTTCCTTTGCTGTAC | 9873 |
rs188929739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058936 | CAACCAGAAATATAA[C/T]TGCATATGAGTTTCC | 9873 |
rs188934820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894623 | TATTTATCCTCAAAA[C/G]GACTTCTTCAAGTAA | 9873 |
rs188935888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130529 | ACCTGCCTTGGGCTG[C/T]AATGGCTGTCCCATT | 9873 |
rs188936640 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914216 | GATGGGGTTTCACCA[C/T]GTTGGCCAGACTGAT | 9873 |
rs188956217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966469 | CCGGACTAAACTGAG[C/T]ATATTACTTTGTTAT | 9873 |
rs188958650 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838772 | TGATTGTAGCAGTAA[C/T]GGATGGGCAAGCCCA | 9873 |
rs188964925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877215 | TAATGATTAGTGTTT[A/G]TTCTCCTGTGATAAG | 9873 |
rs188969663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859594 | AAGGTTCGGTACTAT[C/T]TGTGACTTCAGGCAT | 9873 |
rs188987844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924299 | TTTCTTTTTTTTGAG[A/T]CAGAGTCTTGCTCTA | 9873 |
rs188989972 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007500 | TGGTGGTAGTGGTGG[C/T]TATGCAGGAGGTGAT | 9873 |
rs189020991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978618 | GTGACTGGATTATAG[A/G]AGCGATTTCCCTGAT | 9873 |
rs189021683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888596 | AGAGTTTAGTCTTCG[A/C]GATATATTTTCTTTC | 9873 |
rs189030245 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865596 | CCTTCACAACGAGAA[C/T]AGCCCTTCTTCTTTA | 9873 |
rs189031415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863015 | GTAACCTTGAACTTC[C/T]GGGTTCAAGATACCT | 9873 |
rs189035949 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044863 | ATCACGAGGTCAGGA[A/G]ATCGAGACCATCCTG | 9873 |
rs189046555 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903508 | ACAGGCGTGAGCTAC[C/T]GCGCCCGGCCTGGAA | 9873 |
rs189050305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027293 | GAACTTATTGAGAAC[C/T]AGAGCAAAGGTCACT | 9873 |
rs189054347 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009217 | AATCATACTACAGGC[G/T]GGGTGTGGTGGCTCA | 9873 |
rs189060222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958343 | GCCAATGTGGTGAAA[C/T]TCTGTCTCTATCAAA | 9873 |
rs189072826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063187 | CATATCCAGCCTAAC[C/T]AAGCTTCATAAGCAA | 9873 |
rs189075039 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127157 | TATACTCCAACTTGT[G/T]TCTGTGGAACCACAG | 9873 |
rs189078294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113705 | GTTTTCCAGGCATTT[A/G]AAGAAACACCCATTT | 9873 |
rs189081339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082119 | GAGGTAGGCGGATCA[C/G]GTGGTCAAGAGATTG | 9873 |
rs189097888 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844690 | AAGCTTTCCCCAAGT[C/T]CCAAGATGGGTTAAA | 9873 |
rs189115800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989671 | ATACACATATACATT[C/T]GAGGAGAAGGGATGG | 9873 |
rs189123668 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967959 | AGCCGGGTATGGTGG[C/T]GGGCACCTGTAGTCC | 9873 |
rs189160479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082716 | TTCTAACAATCTCCC[A/G]TATTTTAAAATTTTT | 9873 |
rs189176430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849217 | ATGTATTCACGCCTC[C/T]CTTCCAACATTCATG | 9873 |
rs189186394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860515 | AAATTCAGTAACACA[C/T]TTTTAATTACCCATC | 9873 |
rs189192090 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884442 | AGTAACAGGCCCAGA[A/G]GTAATATAAATTTGG | 9873 |
rs189210868 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838038 | TCAGATCCGGAAGTT[A/C]CATTTCTGCTTTAGC | 9873 |
rs189226497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139269 | GATGAGGCTTACAGA[C/G]CCAATTCCAATTTGA | 9873 |
rs189275882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031116 | GTGAAATAAGCCAGA[C/T]AGAAAGAAGACGACT | 9873 |
rs189283796 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917048 | GGAGTGCAGTGGTAC[A/G]ATCTCAGCTCACTGC | 9873 |
rs189293763 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000571 | TAGTCAAAATGTGTT[A/C]ATTTCCTTTAAATTA | 9873 |
rs189302338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956466 | CTGATACAAGAAATA[C/T]CATAAACTGTGACTT | 9873 |
rs189302446 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067453 | CTGCGCGTTCTGCAC[A/T]TGTATCCCAGAACTT | 9873 |
rs189315874 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881635 | AGATGTGGAATCAAC[C/G]TAAGTGTCCATCAGT | 9873 |
rs189325569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082323 | GCCTGGATCACAGAG[C/T]GAGACTTGTCCCAAA | 9873 |
rs189325945 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962417 | AAAGCTCTTTGATTC[C/T]TCAATAATTTTTAAG | 9873 |
rs189346026 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063854 | TGGGAGACTTTAACA[A/C]CCCACTGTCAATATT | 9873 |
rs189351914 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920934 | AGAGCTCTGGTACAG[G/T]GAAAACAAGAATATA | 9873 |
rs189361588 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103861 | AAAAGTCCCATGAAC[A/C]AAGCAAACTCTCCTC | 9873 |
rs189370237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126641 | GTTATGCTTAACAGA[C/T]ATGCAATAAAATGTT | 9873 |
rs189370769 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889516 | GGAGTTTGAGACCAG[C/T]CTGGGAAACATGGCA | 9873 |
rs189373071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104220 | ATTAAATAGCACATA[C/T]AGTATCATTTACTTT | 9873 |
rs189376734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935993 | GTGGGCTAAAACCAC[A/G]TAATATTTAGGTTGC | 9873 |
rs189383138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955294 | TACTTACTCATTTAT[C/T]ATAAAACATTATTAC | 9873 |
rs189393181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978261 | ACATGTATACATATG[C/T]AACAAACCTGCACAT | 9873 |
rs189396762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854715 | AAAATACTCTGATTC[C/T]ACTTATTTGAGGTAT | 9873 |
rs189406604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875218 | AATAATGGTAGATAA[C/T]AGTATTTGCTACTCC | 9873 |
rs189410587 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903103 | CCAAATAGTGTTTGT[A/G]GAGTATTTCTCAGCA | 9873 |
rs189416999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916528 | CTATGTTGCCTAGGC[A/T]GCTCTTGAACTCCTC | 9873 |
rs189438652 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072860 | CTTCTTGTATAGTAT[A/G]CCCAAGTCTTCATAA | 9873 |
rs189462062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840332 | AAAGCTAATAGGGGT[C/T]AAGGAAAATAAAATT | 9873 |
rs189480763 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906982 | GTGGTAGCTTGATGG[G/T]GACAGCATTGAATCC | 9873 |
rs189526697 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016936 | GATTTTAAACTGCTC[A/G]TTCCAATTATACAAT | 9873 |
rs189529446 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837729 | AGCTGGTTTCCTCCA[C/T]GAGCCACCAGGTTCT | 9873 |
rs189532103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999374 | ACCCAGGCTGGAGGG[C/T]AGTGGCACGATCTCA | 9873 |
rs189546279 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876889 | TATATTCATGATGAA[A/C]TGTCTTTAAAAAATC | 9873 |
rs189558195 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033275 | CCTGGGCAACAGAGC[A/G]AGATTCCGACTCAAA | 9873 |
rs189573466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098610 | ATAGTCCAGGAAAAA[A/G]AAAACAAACATCTAT | 9873 |
rs189590133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086157 | TCACGCCTGTAATCC[C/T]AGCACTTTTGAGAGA | 9873 |
rs189604263 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051668 | TGCAGAGATGTACTG[A/G]CTATGCAACAATAAA | 9873 |
rs189624868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096278 | GGGAACAGTGGCTCA[C/T]GTCTGTAATCCCAGC | 9873 |
rs189631801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056693 | GAGAGCATAACAGAA[C/T]AATAAGTCATATGAC | 9873 |
rs189634855 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877899 | TAGCCCCAGCTATTC[A/G]GGAAATGGAGGTGGG | 9873 |
rs189637821 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074518 | AATTCCAGAACATTG[C/T]ATAACACACCTCAAG | 9873 |
rs189643707 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985136 | AATAAAAATAGAAAA[G/T]TATGTTTAATAAAAT | 9873 |
rs189644324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939836 | GTTTGTCAGGCTGGT[C/G]TTGAACTCCTGACCT | 9873 |
rs189648566 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984322 | TCCCCAACAAGAATA[A/G]AGGTAACCACGTGCG | 9873 |
rs189651189 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926890 | GAATGTCAGCCAGAA[C/T]TATACAGATGTGCAT | 9873 |
rs189657617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118716 | ATGATGATACTATAA[A/T]GATGATGGCAAACAC | 9873 |
rs189661661 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947546 | AGTCACTGAGTCTAG[A/C]AAGAAATGGGTATAT | 9873 |
rs189666268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135848 | TCCTCCCCTCGAAAT[C/T]CCAAAAGATAAGAAC | 9873 |
rs189678401 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848551 | ATATTTAACCCTTCA[C/T]AGATTGTCCATTCCT | 9873 |
rs189681274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022467 | GCTCTCCTACATACA[C/T]GCAATGAACAACTGG | 9873 |
rs189683307 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968878 | ATAGTAACATTAAAA[G/T]ATATTTCTATAAATT | 9873 |
rs189683434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875520 | TTTTTTGTAGAGATG[A/G]GGTCTTGCTATGCTG | 9873 |
rs189685855 | snp | A/C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890659 | AAGGTACTATGGAAA[A/C/G]TGCTTCATATAACTT | 9873 |
rs189690609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910735 | AGAGACCTTTGTTCA[C/T]GTGTTTATCTGCTGA | 9873 |
rs189691958 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037648 | TTAGGGCCCATACTG[A/G]TTATGTTATGAATGT | 9873 |
rs189699139 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867402 | TATGTGAGGAGAATA[C/T]GAAAGCTGTCAAGAA | 9873 |
rs189719184 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092150 | CTTCTTTTTTAGAGG[A/T]AGGGTCTTGCTCCAT | 9873 |
rs189775324 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893778 | CTCTAGTCCCTTTAG[A/C]ATAAAATATTACAAT | 9873 |
rs189800067 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858155 | GGTAATACCTAATAC[A/G]GAGGAAGACAGCTCC | 9873 |
rs189800427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972278 | ACCATGTTTTGATTT[A/G]TATTTTTATGAGTTT | 9873 |
rs189814170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009954 | TAAATCTCGTTAGAC[C/T]TGGGAAGTTTTTGTC | 9873 |
rs189815053 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953278 | GATCTCCAGAAACCT[A/C/G]CTGCTGGTGATGAGT | 9873 |
rs189818767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908273 | ACATTTTCTCTATCC[A/G]TTCATCTGTTGATGG | 9873 |
rs189822186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990917 | AAAAATCAATGAATC[C/T]AGGAGCTGGTTTTTT | 9873 |
rs189840762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040964 | TCCCACATATCAGTG[A/C]GTGAGAACATGTGAT | 9873 |
rs189840977 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997723 | TGTTTTGTTTTGAGA[A/T]AGGGTCTCCCTCTGT | 9873 |
rs189844708 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915446 | AAAGACATATGCCTG[C/T]TTATGTTCATTGCAG | 9873 |
rs189850804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975073 | CCGAAAAAGAACTTG[A/G]CTTTCTGTTCCTGGC | 9873 |
rs189853247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933930 | CTTGGGCAACACAGC[A/G]AGACTCCATCTCTAC | 9873 |
rs189855355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120661 | TTCATCTTGGAAGGC[A/G]GAGGCTGCAGTGAGC | 9873 |
rs189859425 | snp | C/T | 0.000903138 | 0.021231 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077653 | GGATAAACTGTGGTA[C/T]ATCCATACAATGGAA | 9873 |
rs189863288 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930690 | GGAGGCTACAGTAAG[C/T]CAAAATCGTGCCACT | 9873 |
rs189898793 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003872 | AGCACTCTGGGAGGC[A/C]AAGGTGGGCAGACTG | 9873 |
rs189899316 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038369 | AAAAAAAAAGGAAAA[A/G]AAATTCTGATGACTG | 9873 |
rs189903723 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120797 | AAGACAGTCTTGCTC[C/T]GAAAAAGCTCACAGT | 9873 |
rs189910850 | snp | C/G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871605 | CAAGTTGGAGCTGGT[C/G/T]CAGTGGCTTGTACCT | 9873 |
rs189930079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136204 | AGAAGGGACGTAATG[A/G]GGAAGAACTAGACAA | 9873 |
rs189939143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040448 | TCTGGTGTATATTTC[C/T]CAAACACCATACAGT | 9873 |
rs189953401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051268 | TACGGTGAGCCAAGA[C/T]TGCATTATTGCACTT | 9873 |
rs189982556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078998 | TGTTGGGATTACAGG[C/T]GTGCGCTACCGCACC | 9873 |
rs189990903 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854434 | CTGTCTGTCTACCTA[C/T]CTGTCTATCTGGTTA | 9873 |
rs190000462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887080 | TAAGCTCTGAAAATA[C/T]ATATATATATATGAA | 9873 |
rs190026566 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851527 | GGGCGGATCACAAGG[A/G]CAGGAGATCGAGATC | 9873 |
rs190046133 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870744 | TCTCTACTAAAAATA[C/T]AAAAAATTAGCTGGG | 9873 |
rs190050244 | snp | A/T | 0.000433695 | 0.0147194 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840937 | CTGTGAGAATCCTGG[A/T]GACTCAGCATGAAGG | 9873 |
rs190068660 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024507 | TGGCAGAGGGTAAAA[C/G]CTCAGTGTTGGAGTG | 9873 |
rs190075895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950516 | ATATATGCTGTGAGG[C/T]AGAGGTCCAACTTCA | 9873 |
rs190076755 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934135 | AAAAAAAAAAAAAAA[A/G]AGCTATTTAAAGCTT | 9873 |
rs190079731 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030868 | GCAAAAAATCCTGAA[A/T]ACAATATTATTAACT | 9873 |
rs190081817 | snp | A/G | 0.0016993 | 0.0290992 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921955 | CCATCAAGAGCCTGT[A/G]ATAGAGGAGTAAATA | 9873 |
rs190090868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994658 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 9873 |
rs190096243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001303 | AAGCAACATGGCATA[C/T]ACTCTATTCTTCTTA | 9873 |
rs190097592 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065157 | CAAAAAGCTTATCCA[C/T]CATGATCAAATCAGC | 9873 |
rs190116108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028763 | TGGATCATGAGGGCA[G/T]ATTTTCCTCATGCTG | 9873 |
rs190118694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103033 | ATCTACTGTATGATT[C/T]CATTTATATGAAATT | 9873 |
rs190129213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035443 | CGAAGTGCTGGGATT[A/G]CAGGCATGAGCCACT | 9873 |
rs190139090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083672 | AAGTATACCTAGAAT[A/G]GGACCTCCAATTTCA | 9873 |
rs190143877 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138753 | GCTAGGACTACAGGC[A/G]CACGCCACCATGCCT | 9873 |
rs190145498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105588 | TTACATCTACAAAAT[A/G]TACTTACTAGGCAGT | 9873 |
rs190163953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871963 | CAATTTATGTTCTGA[A/C]TTGTATCACTGGGCT | 9873 |
rs190180922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925587 | CATTCAAGAAGGAAT[C/T]TGTTGCCACGGTGTA | 9873 |
rs190220177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098825 | TAAAGGAAAACACAG[G/T]GGCAATTCTTCATGA | 9873 |
rs190254836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108745 | GGCTAATTTTTTTTT[A/G]TATTTTTAGTAGAGA | 9873 |
rs190261433 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874359 | GCCTGGCTAATTTTT[A/T]AAAATTTTTTGTAGA | 9873 |
rs190267731 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987457 | AGGCCTTAAATTCCT[C/T]GAGGGCACAAAGCTT | 9873 |
rs190286665 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885237 | TAAGTGGAAACCAAG[A/T]GAGATTATTTTATGC | 9873 |
rs190293960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112553 | GTTTGGGAAGTTCTC[C/T]GTTGTTATCCCCGTG | 9873 |
rs190301716 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910296 | CGCCTTTGTCCGGCC[A/G]CCCCGTCTGGGAGGT | 9873 |
rs190302225 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133245 | CATAGAGTTACCATA[C/T]GACCCAGACATTCCA | 9873 |
rs190302628 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943678 | TTAAAATATAAAATT[A/C]TATTGGCTGTTTTGT | 9873 |
rs190306157 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915146 | AATCATATGAAAAAA[A/T]CTCAACATCACTGAT | 9873 |
rs190311907 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880687 | TTGGGAGGCTGAGGC[A/G]GGTGGATCCCTTGAG | 9873 |
rs190317672 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933623 | TCTTTTGGTTGCATT[A/G/T]TAAGGAAAAAAAGTT | 9873 |
rs190328057 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965151 | CTGTAGAACAATTCT[G/T]AACAGTGGATACAAC | 9873 |
rs190330340 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887985 | GAAAAGAAGATGTCA[A/C]AACAGGCAAGAGATT | 9873 |
rs190332287 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995590 | GCACCTGTAGTCCCA[A/C]CTACTTGGGAGGCTG | 9873 |
rs190332454 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908885 | TCTCTAACTCCTGGG[A/C]TCAAGCGATCTGCCC | 9873 |
rs190337763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861644 | TCAATATATAGAAAG[A/G]ATAGGCCGGGCGCGC | 9873 |
rs190340712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923070 | TGGTGCCTGGCTTCT[C/G]TTGCCCAGCATAATA | 9873 |
rs190346058 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878221 | GAGTTCAAGGCTATA[C/G]TACACTATGATTGTG | 9873 |
rs190350193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896401 | CCATCCCAGCTTCGC[G/T]TTGTCCTTTTTCACA | 9873 |
rs190354399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980384 | CTGCTTAGATACAGA[C/T]TATCCAGTTATGGGG | 9873 |
rs190357383 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845086 | TGTGACAGCAAACCA[C/G]GGAGGTAGTACACTT | 9873 |
rs190364265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055616 | TTATAATGTATACAA[C/T]ATATTAGTACAGAGT | 9873 |
rs190366587 | snp | A/T | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842969 | AGTTGTAATTTTTTT[A/T]CTCACTGATGAATGA | 9873 |
rs190383163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017906 | AGTATAATAGCTATT[A/C]TTTCTATATTTATTA | 9873 |
rs190387640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945781 | ATTTATGCAGCCAAA[C/T]GATACATGAAAAAAT | 9873 |
rs190421568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909530 | GCCCCTCTGCCCGGC[C/T]GCCCTGTCTGGGAAG | 9873 |
rs190438558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990069 | GAAAGGACTACAGGG[A/G]ATGAGACATCTAGAA | 9873 |
rs190471915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027588 | AGAAAAACCAATTTT[C/G]TGAAGAGAAATTCAA | 9873 |
rs190483440 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054957 | GCTAAATAAAGACAT[A/C]CTTGAGACTGGGTAG | 9873 |
rs190490512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131046 | TTTTAAATACCTGAG[C/T]CCAGTACCTGATCTG | 9873 |
rs190518528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846706 | ACCAGAGCTCCGTTT[C/T]CACCAGTATCTCTCC | 9873 |
rs190541369 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110351 | GGCGATATTTTATTA[C/T]GGCTTCAATCCTGTT | 9873 |
rs190546070 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081124 | TTAAATAATAAACAT[C/G]TCCTATTTACTTGAT | 9873 |
rs190548890 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856157 | ATGTAGAAAACTACG[C/T]TAGCCTCTTTGATGG | 9873 |
rs190552398 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042355 | CACCTTTGTCAAAAA[C/T]CAGTTGGCAGTAAAA | 9873 |
rs190559953 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926165 | GTTCCCAGTAAGGCC[C/T]CACCTTCAGGCCAGG | 9873 |
rs190575648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131995 | ATATATTTCCACAAA[C/T]TACCATCCTCCATGC | 9873 |
rs190581085 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100959 | TCTCCTCACACAGAC[C/T]CTTGTTTTTTACCAA | 9873 |
rs190596897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905602 | TAGCCCCCCACCCCC[C/T]GACAGGTCCCAGTGC | 9873 |
rs190600427 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014124 | AAATCTGTGTGGTTT[C/T]TTTTTTTTTTTTTTT | 9873 |
rs190601612 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864427 | GCATGAGCCTGTAGT[C/T]CCAGCTACTCAGGAG | 9873 |
rs190616605 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024657 | GGATCTAATTAAACT[C/G]AAGAGCTTCTGCACA | 9873 |
rs190618626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007460 | ACCTCATCTCTACAA[A/G]AAAAATTTTAAAATT | 9873 |
rs190633612 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988044 | AACCGCGGAGCCCCT[A/G]AATTTTCACAAGTTG | 9873 |
rs190655223 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917345 | TTTCTGAAGAGAATA[A/T]TCTTTCTCTATTGAA | 9873 |
rs190665296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937356 | TTTAAATAGTCTCTT[C/T]TGTGTGCATTTTTGA | 9873 |
rs190673415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865759 | GTGGGGGTGGGGAGT[C/G]GGAATCTCAGAGTCT | 9873 |
rs190688332 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881745 | AATATAAATGGAACT[A/G]GAGGTCATTATGTTA | 9873 |
rs190695859 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968503 | GATTCCAATACATAG[C/G]ATCAGAATAACTGTG | 9873 |
rs190714429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071462 | CTTGAGAGGTCGAGG[C/T]GGGCAGATCACGAGG | 9873 |
rs190716684 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045974 | TTGCTTATATTTCTA[C/T]AATAATTTCAGTAAT | 9873 |
rs190717521 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982005 | TATATACTAAAACAC[C/T]TAAACCTCTAGGTCT | 9873 |
rs190726646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009367 | CCAGGTGTGGTGGCG[C/T]ACACCTGTAATCCCA | 9873 |
rs190756842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099333 | GTGAAGAAATTAGAA[C/T]CCTCATGCATTGCTG | 9873 |
rs190758003 | snp | G/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938511 | CCTTGCTGGTGTCTA[G/T]GTGTGCCCACAGCCA | 9873 |
rs190758987 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059754 | CCCTAGCTGTGAACA[A/C]TTCCAGAATTCTGGC | 9873 |
rs190762991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032709 | AAGGCTTCCCCAAAG[G/T]AAATGAAAATTGACA | 9873 |
rs190769348 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014886 | TCTCACTCTGTCGCC[C/G]AGGCTGGAGTGCAGT | 9873 |
rs190770993 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010349 | TTTCTTGTATCTCAT[C/T]GAGCTTCTTTAATAT | 9873 |
rs190774583 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019234 | AAAGCAGAATGACAG[C/T]ACTCTAAATTTATGT | 9873 |
rs190778787 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991610 | GCTGGTTCAACATAC[G/T]CAAATCAATAAACAT | 9873 |
rs190780372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046563 | AGAAATATAAATTGG[C/T]GTAGCATTTTAAATT | 9873 |
rs190789717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121840 | TCAGAGTTCCTGATG[A/C]AGGAGATTAGGGATA | 9873 |
rs190852823 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919231 | ACATGGCATAAAACT[C/T]GTAGGCCTCTTCTGG | 9873 |
rs190880695 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883061 | AATGGGAAAAGCATA[A/C]TCTTTAAAATATGAT | 9873 |
rs190899543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056361 | ACAGGAGTTATTTTT[C/T]ACTGCTAGGGAATAC | 9873 |
rs190899721 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036386 | TCACAACGTTATATC[A/G]GTCTTTGGAGTCAAA | 9873 |
rs190907527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899434 | GCAAACCAGAACCAC[A/G]AGATACTATTTCATA | 9873 |
rs190911109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855401 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC | 9873 |
rs190914713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018549 | AATCATTATATCCCC[A/G]GCTATAGCAGATCAC | 9873 |
rs190923921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005600 | TTCTCTTCTCTAACT[A/G]CATTCACTCTGTTGA | 9873 |
rs190944507 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959036 | GTGTGTACATCCATG[A/C]GTGCATGGGACACAC | 9873 |
rs190948531 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922374 | TTATACATTGGTATA[G/T]GTATATTTACTGAAC | 9873 |
rs190950850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928604 | CTCAACTAGCTCTTC[C/T]TTAGCGTTTTCACAA | 9873 |
rs190965840 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001946 | ATGCCTTAGTCAATT[A/C]TAGCATGCTCCTACA | 9873 |
rs190974896 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980957 | GGGCATTATCACCTT[A/T]ACATTAATTCAGAAA | 9873 |
rs190984914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028188 | GTACCTGGAAAAGCC[A/G]CAGGCACTCAATGGC | 9873 |
rs190984973 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998133 | AGACATGAACAGAGT[A/C]AAAAGGTCTAACAGC | 9873 |
rs190986362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937795 | ATACAGGGTGCTAGA[A/G]GAGAGGCACCTAGAC | 9873 |
rs191003486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119660 | CACTGTGTTGCCCAG[C/G]TTGGTCTCACTCCTG | 9873 |
rs191010171 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064456 | CAGAACTGAAGGAGA[C/T]AGAAACAAGAAAAAC | 9873 |
rs191014379 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960114 | ACTGTACAAAAAGCA[C/T]AGTGCCAGGATCTAT | 9873 |
rs191015771 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999315 | ATCTTACCAAAGATT[C/T]TTTTTTTTTTTTTTT | 9873 |
rs191029087 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002161 | GTGGTCAACAGATGA[C/T]AGTGTAGAAGCAAGA | 9873 |
rs191057746 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075046 | GCCCAATCAAGATAT[G/T]AAAAGTTCCTCTAAT | 9873 |
rs191091455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878141 | CCCTCTGGCTGGGCA[C/T]AGTGGCATGCAGTTG | 9873 |
rs191098015 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851700 | GTGAGCCGAGATTGT[A/G]CCACTGCACTCCGGC | 9873 |
rs191133172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986668 | CCCAAATAGGCTGAG[C/T]TGCATGTAGATCTTC | 9873 |
rs191155895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943095 | CTCCCGGGTTCAAGT[A/G]ATTCTCCTTCCTTGG | 9873 |
rs191161055 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023460 | CATCACTTGTCATTA[C/T]GGAAATGCAAACTAA | 9873 |
rs191183511 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908585 | AGCCACCTGAACTAG[C/G]ATGATATAATATCTT | 9873 |
rs191184885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106417 | TCTCCAAAAAAAAAA[A/G]AAAAAGAAAAAGAAA | 9873 |
rs191189848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878852 | TGGCTCATGCTTGTA[A/G]TCCCAGCACTTTGGG | 9873 |
rs191191035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024111 | CAAAGAACTTTGACA[A/G]TACCCACAGAACTTT | 9873 |
rs191195099 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129025 | TACAGGCATGTGCCA[C/T]CGTGCCTGGCTAATT | 9873 |
rs191197672 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029810 | AGAGAAATTAGTAAG[A/T]CACCACAATATACAG | 9873 |
rs191203349 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011727 | CATGGCCAGCACTAC[A/T]GAAGTCTACAGTGGG | 9873 |
rs191203925 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084635 | TGGCCTCAAAGCAAT[C/T]CTCCTGCCTTGGCCT | 9873 |
rs191230535 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061285 | GAACAGATACTGTGC[A/T]TGTCGCATGGTTTTC | 9873 |
rs191233090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949399 | AGGTTACAGTGAGCC[A/G]AGATCATGCCACTGC | 9873 |
rs191237251 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892908 | CGTGCGTGGCTGGTA[A/T]TTTTTTTTTTAAGAC | 9873 |
rs191241979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096517 | GATTGTGCTGCTGCA[C/T]TCCAGCCTGGGTGGC | 9873 |
rs191262507 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914760 | AAAGACTTAAATGTA[A/C]AACCCGAAACTATAA | 9873 |
rs191265796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994193 | ATGCTAGATGCTTCC[C/T]TACTGGCAAATTGTG | 9873 |
rs191267726 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913453 | TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCGCC | 9873 |
rs191272653 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971693 | TGAATGACCCTGGAA[A/G]GAGATTCTTCCCCAG | 9873 |
rs191274601 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929548 | GGAAGTGGATGATAA[C/G]CCTATGATTTGCTCC | 9873 |
rs191276265 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952575 | AGTGATCTACCGGCC[C/T]CGGCCTCTCAAAGTG | 9873 |
rs191276485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907195 | TTTTGTATCCTGAGA[C/G]TTTGCTGAAGTTGCT | 9873 |
rs191306923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127647 | CTCCTCAGATAAACA[C/G]CTTCAGACTTGATAC | 9873 |
rs191321953 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057078 | ACAGAGCAAGACTCC[A/G]ACTCAAAAACTAAAA | 9873 |
rs191338603 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896207 | ACATCAGAAATTTAG[G/T]GTCAGCTTTTTGCTG | 9873 |
rs191346354 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099686 | AGGCTTAGCGGCGCT[C/T]ACCACCCTGGTTCTT | 9873 |
rs191350191 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73140034 | CTATAGCCTTACCTC[A/G]TATCTTCAAGCAAAT | 9873 |
rs191351993 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058273 | GCATTAACACTTGAG[G/T]TTATTACAGCACAGA | 9873 |
rs191366525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861078 | TCAAGAAAATAGAAA[A/G]GAGAAAAACGAGGGA | 9873 |
rs191384737 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909194 | GGCACACGCCGCCAC[A/G]CCTGACTGGTTTTTG | 9873 |
rs191408308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873087 | ATAATCCCAGCACTT[C/T]GGGAGGCTGAGGCGG | 9873 |
rs191420783 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888693 | GCATGATCTTACCTC[A/G]ATGTAACCTCCACCT | 9873 |
rs191432676 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006819 | CACTGTTGTATGTTC[A/G]GCACAGGGTATGGCA | 9873 |
rs191446100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852772 | ATGACAAGTTGAATA[A/C]AGAAAATGTGGTACA | 9873 |
rs191451802 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869875 | GACCTCATCATGTTG[C/T]TCCCCAGTTTAAAAA | 9873 |
rs191465767 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042209 | GGACTACAGGCATGC[A/G]CCACTGCACCCGGCT | 9873 |
rs191478698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085785 | AAATCTGGTATTCTG[G/T]TTCAAGTTGATGTTT | 9873 |
rs191483241 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120589 | ACAAAATTAGCCGGG[C/G]GTGGTGGTGCATGCC | 9873 |
rs191488916 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107935 | GGATATATACCCAGC[A/G]CTGTGATTGATGGAT | 9873 |
rs191494064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077094 | CAGCCTGAGACTCTG[C/T]CTCAAAAAAAAAAAA | 9873 |
rs191499485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097970 | ATAGCCCATGGTGCC[C/T]AGCTCTTCTTCTAAT | 9873 |
rs191500216 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086978 | AAATATTGTATGATT[A/C]CAATTATATGAGGTC | 9873 |
rs191500976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066557 | TCAGAGTGAACAGGC[A/C]ACCTACAGAATGGGA | 9873 |
rs191503604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932786 | CAGGTCTGTCTGTTT[A/G]CCATTCCATCTTCTG | 9873 |
rs191509868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137098 | TCATTCCACTTACTA[A/G]GGCAGACAAGAGAAG | 9873 |
rs191521488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974423 | AAAAGTCCCACTTCT[C/T]AGTATTGTTGCATTG | 9873 |
rs191522557 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130091 | ATGTTAGCCAGGATG[A/G]TCTCAATCTCCTGAT | 9873 |
rs191533302 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014715 | TGCTATTGTTTGAAG[A/G]GTATTTGGTCATAAT | 9873 |
rs191540603 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036336 | AGACAAAAAAAAAAA[A/C]CCCAAGCTTCATAAT | 9873 |
rs191547534 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974840 | AAGCAAGAGAAGCAG[A/G]GATTTAACAGAATTA | 9873 |
rs191560483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051213 | CCAGTGGTGTTGCAT[A/G]CTGAGGAGGGAAAAT | 9873 |
rs191562122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030408 | TGAATATACAAAACT[C/T]AATTTACCATACATA | 9873 |
rs191573725 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011934 | TAGTGGAGGAGGTAC[C/G]AAGTGCCCCTAGTCA | 9873 |
rs191597009 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122344 | AAGAAACATCAAGAC[A/G]TAGACTCTGCTGCAG | 9873 |
rs191650364 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952678 | TAAGAGCTTATTGGT[A/T]GAGATGAGACATTAA | 9873 |
rs191692914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969243 | CGGAGCTGCATTCCA[A/G]TGTTTATTATCTTCA | 9873 |
rs191693431 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850722 | ATATTTATCAGTATC[C/T]TTTCACTTTTCACTG | 9873 |
rs191705546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886166 | TTGGGTCCCTGAAAG[A/C]TGCTTGCCCAGAATC | 9873 |
rs191708354 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909408 | ACCTCCCAGCTGCCT[G/T]CCTTGGCCTCCAAAA | 9873 |
rs191710517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008964 | ATATAAATAAGCTTA[A/C]TTAAAAGTCATTAGA | 9873 |
rs191718941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989225 | TCAGTACGTTCAGTG[C/T]CCTTCAAATTGCAGA | 9873 |
rs191719006 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032919 | AAATCAAGCTTGCGA[A/G]CAGTGCAGTGCCATT | 9873 |
rs191721065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015420 | ATATTTAGAATTTAT[G/T]TCAAAAGTATCAGTG | 9873 |
rs191721309 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924696 | TTTTTTTTTTTTTTT[A/T]AAATACACAAATTCT | 9873 |
rs191723184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927796 | GGCAGAGAAGCCTAC[C/T]ATCCTGAATAGGGTC | 9873 |
rs191726173 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967789 | ATATCTAATTTTTTT[A/T]AAAAAGAAGTGGGCA | 9873 |
rs191732342 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944935 | AACATTCCATGCTCA[C/G]GGGTAGGAAGAATCA | 9873 |
rs191753097 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069085 | GGAAGCCAAGGTGGG[C/T]TAATCACCTGAGGTC | 9873 |
rs191753262 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891942 | AATTACTTGAAACAA[A/C]AATTTTCTTATTACT | 9873 |
rs191756586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889065 | GTTCATGCCATTCTC[C/T]TGCCTCAACCTCCCG | 9873 |
rs191775254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855955 | CTAATAAAGAAGAGA[C/G]AAACAGCCTCAAATA | 9873 |
rs191800010 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996232 | CCCACTCTGTTATTT[A/C]CTACCTAAGTCTCTT | 9873 |
rs191829901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032162 | ACTCTAGAATACATA[C/T]GAACTTGGAAATGAG | 9873 |
rs191841276 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088936 | AATAAGGACATTCAC[A/G]TGAAGTCCACAAGAA | 9873 |
rs191851035 | snp | C/T | | | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843922 | CTGAGGTGGGAGGAT[C/T]GCTTGAGCCTGGGAG | 9873 |
rs191853918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053881 | TGACCATTTAAATTA[C/T]AGATTGAAATGTAAC | 9873 |
rs191855649 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070394 | CACGCCAGTCGTAAA[A/G]TAGATACTTGATAAA | 9873 |
rs191857841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863534 | AAAAATTTGTGCTCT[C/T]TGAAAGGTATTAAGG | 9873 |
rs191868874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111684 | CTTTCCTTCCTTCCT[A/G]TCTTCCTTTTAGTGA | 9873 |
rs191872423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070093 | GTAAAAAAGGAAACT[A/T]ATCAGTAACAAGAAT | 9873 |
rs191888101 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847417 | ACTAATGACCTACTA[A/C/T]GTGCTGGGCATTGTC | 9873 |
rs191903064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882124 | CACTCCAGCCTGGGT[A/G]ACAGCAAGACTCCGT | 9873 |
rs191940194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140545 | AAGAGTGCCTGATAC[C/T]CAATGACCAATATTT | 9873 |
rs191959813 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844828 | ATCAATTTCCCATTT[C/T]ATGAACATTAAAACA | 9873 |
rs191974030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992394 | CAATGACTTTCTTCA[C/T]AGAATTGGAAAAGAC | 9873 |
rs191979902 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864221 | AAAATGTAAGCAATA[A/G]AAGAACAGGGTGGGC | 9873 |
rs191989417 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093046 | GAGGCTGGAGGCTAA[A/G]GCCAGCCGCATGAGT | 9873 |
rs191991072 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065396 | CAAACCCACAGCCAA[C/T]ATCATACTGAATGGG | 9873 |
rs192004615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029092 | CCAGAAAGGGCACCA[C/T]AAATATAATGGTGTA | 9873 |
rs192020347 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948851 | TTTATATTTTTAGTA[C/G]AGATGGGGTTTCACC | 9873 |
rs192022594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948250 | TGGACTCAAGCAATC[C/T]ACCCACCTCAGCCTC | 9873 |
rs192032705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918412 | TGTCTAGGACTTCCA[A/G]TACAATGGTTAATAG | 9873 |
rs192046403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876065 | TGGCTGACACCTGTG[A/G]TCCCCACATTTTGGA | 9873 |
rs192058290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911046 | GCCTGTGCTTGCAGG[A/G]TATTACTCAATCTTT | 9873 |
rs192090261 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135144 | CAGGCATAAGCCACC[A/G]CACCCAGCCTCCTGA | 9873 |
rs192105075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132959 | AAATGGGCAAAGTAC[C/T]TGAATAGACATTTCT | 9873 |
rs192110798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965720 | ATTCTATGTACACCC[C/T]TCACCCAAGATAACC | 9873 |
rs192112753 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935822 | AGGAAACAAATAAGG[A/G]AGTTTATGTCTGTAA | 9873 |
rs192120707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954682 | AAATCAAAGGCTGAG[C/T]AGGTAACCAGGCTGG | 9873 |
rs192137030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880500 | ACATTGGGGAAAGGA[C/T]ACCCTCTTCAATAAA | 9873 |
rs192139113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900778 | AGAGCTACTTAAAGT[A/G]TAAGAAAAGTAATGA | 9873 |
rs192149361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133725 | ATGAACCCAGGAGGC[A/G]GAGGTTACAACGAGC | 9873 |
rs192149530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082128 | GGATCACGTGGTCAA[A/G]AGATTGAGACCATCC | 9873 |
rs192154379 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916232 | ATTAAAGGGAAAAAA[A/T]GGTTTATCAATTTTG | 9873 |
rs192157021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876860 | TATTATTATATATAC[G/T]TCCAGGATTTTAATA | 9873 |
rs192158918 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103160 | GTTCTATATATTGAG[G/T]GTAGTAGTGTTTAGT | 9873 |
rs192162330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088500 | GTACTAAAATAGTAA[G/T]GAAAGTTTTCTCTGG | 9873 |
rs192191951 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866276 | GTTTTGTTTTGTTTT[G/T]TTTGTTTTTTGAGAC | 9873 |
rs192192296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125419 | ATTAAGAATGCATGG[C/T]GTAGATCGAGTGTGG | 9873 |
rs192234537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050258 | GTTTGCCAGCCTCTA[C/T]ATTAAAAAGAGGGCT | 9873 |
rs192236942 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984336 | AAAGGTAACCACGTG[A/C]GGAAAACATTTATAC | 9873 |
rs192263780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085137 | TTTCAAAATAACAAA[C/T]GGAAGAAGTTTCACC | 9873 |
rs192263892 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021727 | AACTTAAAAAAAAAG[C/T]TCATTCATGACAGAA | 9873 |
rs192265166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938986 | CATTTAATAAAAGTG[A/G]CCTCTGAGCTACTAA | 9873 |
rs192274627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961030 | CCTAGGAATGGGGAG[C/G]TAACACACATGTGAG | 9873 |
rs192281172 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940195 | CTTTTAAACTCATCA[C/T]TACTGAGATTCTAAA | 9873 |
rs192286311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883506 | AATACTTTACTAAGG[G/T]GGATATATGAAGGGC | 9873 |
rs192286560 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982825 | TTACCCATAAATTCA[C/G]GATAAACGTAATGAA | 9873 |
rs192289484 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838207 | GTGGAAGAGATGTGC[A/G]TTAATGCAATTGGTG | 9873 |
rs192292988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010670 | AGTGTCAGTGGTGTT[C/T]GTAATTTATTCAGTG | 9873 |
rs192298962 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906052 | TAATTTACACTCCCA[C/T]CAACAGTGTAAAAGT | 9873 |
rs192305686 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919472 | AGAGAATATAGTAGA[A/T]GATCATGGAAAGCAC | 9873 |
rs192309940 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848919 | TTTTCAAAAGATTAT[A/C]AAAACGATTTACATT | 9873 |
rs192313668 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969773 | CAGCAAACTCCACAC[C/T]ATGTTATTTGTGATA | 9873 |
rs192322684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047883 | ATCTCATTTAAGCTT[A/G]GCAACAACTGTGAGT | 9873 |
rs192329800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118210 | TATAATCCCAGCAAC[A/T]TGGGAGGCTGAGGCA | 9873 |
rs192342195 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073986 | AACTGATTCTAAAAT[G/T]TATAAGAAAATATAA | 9873 |
rs192348382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102569 | CTCCTCTAAAACTCA[C/T]GTTGAAGTTTAATTG | 9873 |
rs192353971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124202 | ACTCATGGATGGGAA[C/T]TGAACAATGAGAACA | 9873 |
rs192356667 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071555 | AAAAAAAAAAAATTA[G/T]CTGGGCATGGTGGTG | 9873 |
rs192358457 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081159 | ACTTTAAATCGACCA[A/G]GCACTGTGGCTCATG | 9873 |
rs192368433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055001 | GTTTAATGGACTGTG[A/G]TTCCACGTGGCTGGG | 9873 |
rs192368532 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033499 | ACTCTGACCCCTCAC[A/G]TTTTAGATCTACTAG | 9873 |
rs192372894 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905358 | CAGGACTACAATGTG[C/T]AATAATCATATCAAG | 9873 |
rs192385240 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846094 | GATAGATAGATAGAT[A/T]AGTAGTTACGATTAC | 9873 |
rs192385945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129809 | GGTTGGGGACCACTG[C/G]TGTAAACTAGCACTT | 9873 |
rs192398642 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842881 | CTGGTAAGATAATTA[A/C]CAGCCGGTTGCTTTT | 9873 |
rs192426140 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924503 | TAGCCAGGATGGTCT[C/T]GATCTCCTGATCTCG | 9873 |
rs192428711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017099 | ACAATCCTCCCAACT[C/T]AGCCTCCCAAGTACC | 9873 |
rs192430829 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999444 | CCTGTCTCAGCCTCC[C/G/T]GAGTAGCTGGAACTA | 9873 |
rs192439617 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978292 | TGTGCACATGTACCC[C/T]AGAACTTAAAGTATA | 9873 |
rs192472611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863026 | CTTCTGGGTTCAAGA[C/T]ACCTTCTTGCTTTAG | 9873 |
rs192523772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962155 | GGACCACTGGGGGGA[A/G]TCTCTGAGACCCTTT | 9873 |
rs192537114 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893646 | TCTTTTAAAAATGTA[C/T]TTGATACAAAAATTA | 9873 |
rs192538959 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021074 | GTAGAGATGGGGTCT[C/T]GCTATGTTGCCCAGG | 9873 |
rs192550766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002925 | TGAAAGCTCCATGAA[A/G]GCAGGGGTGTATGTC | 9873 |
rs192556299 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912224 | CTTGTCATGTTCCAA[A/G]TCTTAGAGGAAACGC | 9873 |
rs192556824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983595 | AATAGAAATATTCTT[C/T]TGCATAAAACTTTTC | 9873 |
rs192575341 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038576 | CTGGCAACGATTATC[C/T]TAAGCAAACTAACAC | 9873 |
rs192581474 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876757 | TCAATTACTGAAAGA[C/G]GGATCCTAAAGACTC | 9873 |
rs192582257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971969 | TTATGATAGTGACAA[C/T]ATGGTTATACATATT | 9873 |
rs192585468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002857 | AGCACTTTTCTTTTA[A/G]TTATAAATATTTTAA | 9873 |
rs192587919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856488 | TCCCATAAATATGTA[C/T]AAATATTATGTGTCA | 9873 |
rs192603746 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892850 | ACCTCGTGATCCACC[A/C]GCCTCGGCCTCCCAA | 9873 |
rs192605891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130648 | AGGTATTACCAAAAC[C/T]CTAATTCTTTCAATT | 9873 |
rs192624511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108533 | TAGCAGTTTCATAGA[C/T]TGAGATTTTAGATTT | 9873 |
rs192639454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003728 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 9873 |
rs192644353 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057918 | AGAGTCTCGCTCTGT[A/C]GCCCAGGCTGGAGTG | 9873 |
rs192658767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076413 | TAAGAACCTCAAAAA[C/T]ATCTGCTAAGCGAAA | 9873 |
rs192663545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106875 | ATTCTATGATGTTGA[C/T]ACAAGGATGAAATTA | 9873 |
rs192667505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039906 | TTAAATTTTCATATC[C/T]CTAATTAATATTCAT | 9873 |
rs192670225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038670 | ATGGACATAAACATG[A/G]GAATAATAAACACTA | 9873 |
rs192670960 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066239 | CCTGACACAAACAAG[C/T]AATGGGGAAAAGATT | 9873 |
rs192685910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921255 | ACTGCAAAACATTTT[A/C]ATCTATCAAATCTTG | 9873 |
rs192702404 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962680 | GATTTCCTATCAAAT[C/T]CTGGAAAAGATGGTT | 9873 |
rs192707079 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998674 | GGATTTAAAAAGTAA[C/G]AAGCTAATAGTGGAG | 9873 |
rs192727732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953526 | ATTTCAACCACATGA[A/C]TTTATTGAACATGAA | 9873 |
rs192736109 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853829 | GTTATGTATCTTAAA[A/G]GGGACTAATATCCAG | 9873 |
rs192739088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915832 | CAAAAACAAAAAACA[A/C]AAAGAAAAGAAAAGA | 9873 |
rs192752692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879319 | CAAAACAAAACTCAA[C/T]AGTCTTTATAAGAAG | 9873 |
rs192756400 | snp | A/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143982 | CAAGGGGACAGGTGG[A/T]TGGAGGCCCAGGGCC | 9873 |
rs192787151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026903 | CTTGCTTTCCCTTTG[C/T]CTTCTACCATGATTT | 9873 |
rs192793408 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102980 | TACACTAAAAAAGCA[A/T]ATTACACTATTAAGT | 9873 |
rs192794725 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843644 | TGATTTTGAGAAACA[A/T]GTTGAACATAAAAAT | 9873 |
rs192800451 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062668 | AATAGCCAAATCGAT[A/C]AAGAGGAAGAAAGGA | 9873 |
rs192808587 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872275 | TTGGCACACAACTTT[A/T]TTTTTCTTTTCTTTT | 9873 |
rs192816074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909020 | CCCCATTTTTAAATC[A/G]AATTATTAAATTTTT | 9873 |
rs192839956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994591 | ACTCACGGTGAAACC[A/C]CGTCTCTACTAAAAA | 9873 |
rs192844531 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019770 | ACATTTCTGAAAGCA[C/T]TCTATGCTTAAATTA | 9873 |
rs192853753 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949792 | TGATGGACATTTGGG[A/T]TGTTTCCACCTTTGG | 9873 |
rs192858401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016313 | GTCTCAAAAAAAAAA[A/C]AAAACAAAACCCAAT | 9873 |
rs192871727 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090375 | GGACTACAGACGCCC[A/G]CCACTACGCCCAGCT | 9873 |
rs192872573 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054180 | TTGACAGAGACCATA[C/T]GGCCCTCAAAGCATA | 9873 |
rs192892249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977771 | GATTCCTCAAGGATC[C/T]AGAACTAGAAATACC | 9873 |
rs192897489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943828 | CAGTTAGCACATCTA[C/T]AATTAAATATTTGTT | 9873 |
rs192938520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900452 | AAGATTTAGGGCTGC[A/G]GTTGGGCTGGGAAAA | 9873 |
rs192947505 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873679 | GACTTACCCCTGTGG[G/T]TTTTTTTGTAAGTTT | 9873 |
rs192948695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934636 | GCTGTGCTTGGCCAT[A/G]AATTTCTTAATCAAT | 9873 |
rs192954128 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893872 | CATTCCAATATTCTT[C/G]ATATATTAGTCTTTA | 9873 |
rs192962601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930037 | AGGCATTTATCTTAA[C/T]TGGGTCACCTTTATT | 9873 |
rs192966461 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967623 | GGAGTAGGGAGAACA[A/C]AAAATGACAGCCAAT | 9873 |
rs192967860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858534 | AGAAGACCAAATACC[A/G]CAAATTCTCATTTGT | 9873 |
rs192969098 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124578 | CTGGCCAACATGGTG[A/G]AACCCCGCCTCTACT | 9873 |
rs192991765 | snp | A/G | 0.00835973 | 0.0641091 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044831 | ATCCCAGTACTTTGG[A/G]AGGCCGAGGCAGGTG | 9873 |
rs193011273 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081931 | TTCAAGATCGGGCGC[A/G]GTGACTCACGCCTGT | 9873 |
rs193015275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888370 | CACAGACATCATTGG[C/T]GATTTTGGTAAGCTT | 9873 |
rs193026056 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016503 | CTTTTAACTATTTGA[C/T]TAGCCATAAAAACAA | 9873 |
rs193026093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114840 | CTCCTCTTCTCAAGC[A/G]GAAGGAGGGGGTCTT | 9873 |
rs193028483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007710 | GAAGAGGTCACACAA[A/G]GCTACAAATGTGGTA | 9873 |
rs193030796 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852001 | CCTGCCTCAGCCTCC[C/T]AAATAGATGGGACTA | 9873 |
rs193038651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966545 | GCCTGCATAGCTTCA[C/T]TGCAAGCTCCCTGCA | 9873 |
rs193048075 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044459 | GTGGCACACACCTAT[A/T]GTCCTAGCTACTCAG | 9873 |
rs193061979 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033245 | GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC | 9873 |
rs193069365 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998906 | TGCTATGCAAAACAA[C/T]TCTGGTCATTTGGGA | 9873 |
rs193074617 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070752 | TTAAAAAAAAAAAAG[A/C]AATTGAACAAGTTAT | 9873 |
rs193104091 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920678 | TTTTCCCCCAACATT[A/C]TTTTCTGAAAAATTC | 9873 |
rs193113592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883886 | GCAGTGAGTTGAGAT[C/T]GTGCCACTGCACTCC | 9873 |
rs193124741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849502 | TAAGAAGGAACTATT[C/T]GAGCTGAGCTTCAAT | 9873 |
rs193128718 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923635 | CCTACTCAAGTCCTT[A/C]ACTCATTTTTAAATT | 9873 |
rs193138368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030920 | ATATCTCTATACTTG[C/T]GCGTCCTGAATTTCT | 9873 |
rs193150069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136392 | TGGTAAGACCCCATG[A/T]CTACAAAAAACACAA | 9873 |
rs193150356 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097185 | TTTTTGTATTTTTTC[A/G]TAGAGATGGGGTTTC | 9873 |
rs193151549 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066922 | TTGTGGAAGACAGTG[C/T]AGCGATTCCTCAAGG | 9873 |
rs193171980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112962 | TGAGCCACTGCCCTC[A/G]GCCAGATATGCCCTT | 9873 |
rs193181761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913925 | TGCTCAAATAAATTA[C/G]AGATGATACAAACAA | 9873 |
rs193183004 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898738 | TTTCTATTTTTTTTT[A/T]TTTTTTTTAAAGACA | 9873 |
rs193212315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134118 | AAAAAAAAACTCTAG[A/C]CCAGATTAGATTACC | 9873 |
rs193214932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090959 | TGTCAACTACTAATC[C/T]AATTTTTTGTCTCTA | 9873 |
rs193219671 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988237 | AGCTCTCCTTCTCAC[A/G]GATGTCTTCAGAGTC | 9873 |
rs193225680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062548 | GAACCTTGAAAAAAC[A/G]TTAGACGAATTGCTA | 9873 |
rs193227612 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025283 | GAAAATGTGGTATAT[A/G]TATACCATGGAGTAC | 9873 |
rs193262030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939383 | CTTTCTAAGGAATGG[C/T]TTTTAAATTATTAAA | 9873 |
rs193267770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869067 | GTGTACCACCACACC[C/T]GGCTAATTTTTGTAT | 9873 |
rs193269410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906827 | TTTTGGTTACTGTAG[C/T]CTTGTAGTATAGTTT | 9873 |
rs193297324 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120282 | GAAGATTACATATTA[C/G/T]AATGTAGCATATGGT | 9873 |
rs193299512 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085973 | TACTAAACAAAGATA[C/G]TAAAACAATGGTTTT | 9873 |
rs193300514 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051323 | CTAGCTCTAAAAAAT[A/G]AAAAAATAAAAAATT | 9873 |
rs199509377 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111834 | TTTTAAACTGATGAC[-/A]AACACTGATTGCATA | 9873 |
rs199515499 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907496 | AACTCTTATTATTTT[C/G]AGATATGTTCCAACA | 9873 |
rs199515890 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956825 | ATGATTTCATAGTGG[A/G]AAAAAAAAAAAAACC | 9873 |
rs199517517 | in-del | -/AGGAGG | 0.0359534 | 0.129167 | cds-indel, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73141927 | GCGTTAGCAAGGACC[-/AGGAGG]AGGAGGAGGGCCGGA | 9873 |
rs199528205 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011057 | TTGTAGTGGCAGGGG[A/C]GGGTAGAACCAACCT | 9873 |
rs199534784 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950637 | ACAATCAGCTACTGA[C/T]GTATGATTAGTAGTC | 9873 |
rs199550363 | in-del | -/TATTTATTTATA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903196 | AGGAATTTATTTATT[-/TATTTATTTATA]TATTTATTTATTTAT | 9873 |
rs199550489 | snp | A/C | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143612 | TTTTTTTTTTTTTTT[A/C]AGTCACGGGGCTGTG | 9873 |
rs199617683 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049434 | TGAACTAAATAAACT[-/A]ACAAATTTTTATGAT | 9873 |
rs199617864 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039930 | TATTCATGAGGATAT[A/G]ACAAAAGCAGTTATA | 9873 |
rs199623106 | snp | A/G | 2.11584e-05 | 0.0032525 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841462 | CCCTTACCGTTTGCT[A/G]AAGGAGACCGGGGAA | 9873 |
rs199623642 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116952 | TTTCCATTTTTCCCC[A/C]AAAAAAATCACTATT | 9873 |
rs199632936 | in-del | -/AATAT | 0.0228947 | 0.104514 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033990 | AATAGAAATCATGAA[-/AATAT]AATAGACAATTTTAA | 9873 |
rs199660269 | snp | C/T | 0.000711385 | 0.0188464 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984258 | AGTGCAAACTGATAT[C/T]GTACTGCAAAACACA | 9873 |
rs199682597 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866257 | CAACTCTGTTCTGTT[C/T]TTTGTTTTGTTTTGT | 9873 |
rs199698613 | in-del | -/AAAT | 0.0528381 | 0.153711 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846046 | TATTGAAGGGATTAC[-/AAAT]AAATAGATAGATAGA | 9873 |
rs199723808 | snp | C/T | 5.7468e-05 | 0.0053601 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73000999 | CAATACCCTTTTTAG[C/T]TGCTGTTCTTTTAAG | 9873 |
rs199757942 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864608 | TGTTTGTCAATTAAA[A/T]AATAAATAAATAAGA | 9873 |
rs199788957 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957020 | CAAAGGACTCTAGTC[-/TT]TTTTTTTTTTTCTTC | 9873 |
rs199797068 | in-del | -/TTA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097382 | GTTTATTTTATTTAT[-/TTA]TTTTTTTTTTTTGCA | 9873 |
rs199797090 | in-del | -/TTTG | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866268 | TGTTTTTTGTTTTGT[-/TTTG]TTTTTTTTGTTTTTT | 9873 |
rs199841948 | in-del | -/T | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073833 | GTACATGTGCAAGGA[-/T]TTTTTTTTTCTTTTT | 9873 |
rs199843128 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916123 | GGTACTAGGCTTAAT[-/A]ACGTGGGTGATAAAA | 9873 |
rs199857250 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082637 | CATTATTTATAATGA[A/G]AATAAAAACAGTAGC | 9873 |
rs199859279 | in-del | -/TATAATA/TATAATATA/TATAATATACTGAATGCT/TATAATATACTGAATGCTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907441 | TGCTTCCAGTTTTTG[lengthTooLong]CCCATTCAGTATAAT | 9873 |
rs199874957 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069019 | CCATCTCCAAAAAAC[-/A]AAAAAAAAAGGCCAG | 9873 |
rs199878479 | in-del | -/GA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956824 | GATGATTTCATAGTG[-/GA]AAAAAAAAAAAAACC | 9873 |
rs199882651 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039927 | AATATTCATGAGGAT[-/A]ATCACAAAAGCAGTT | 9873 |
rs199886576 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898746 | TTTTTTTTTTTTTTT[A/T]AAAGACAGGGTCTTG | 9873 |
rs199889884 | in-del | -/AAGCAGAG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917004 | TTTTTTTTTTTTTTG[-/AAGCAGAG]TGTTGCTCTGTCGCC | 9873 |
rs199892054 | snp | A/G | 3.54497e-05 | 0.00420994 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73001104 | CTGCATTGTTCCCTC[A/G]AGAAAAGATTTCCAA | 9873 |
rs199959976 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023582 | CTCCTTCAACGGTGG[G/T]GGGAATGCAAAATAG | 9873 |
rs199961304 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896947 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 9873 |
rs199969266 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045521 | TTGGAACCAACCCAG[A/C]TGTCCAACAATGATA | 9873 |
rs199986930 | in-del | -/GGC | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972751 | CATAAGCCCCTTGTG[-/GGC]GGCACCAGAGAATAA | 9873 |
rs200023715 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843195 | ACGAGTTCTGCTTCC[A/G]TGGAATTGCTGGACG | 9873 |
rs200038057 | in-del | -/AGTTGTC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923961 | TAAATAAATAAATAA[-/AGTTGTC]TTTTTGTTGTTGGGT | 9873 |
rs200056109 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083570 | AGAAAAAAAAAAAAA[-/A]CAAGAAAGAAATAAC | 9873 |
rs200071474 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030103 | AATGCCATTAGTTTG[-/A]AAATATTTTTGCCTA | 9873 |
rs200093798 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099280 | TAAAACAACACAAAA[A/C]AAAACAAAAACAGAA | 9873 |
rs200106413 | in-del | -/T/TT/TTT | 0.406641 | 0.194842 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914963 | TTTTTTTTTTTTTTT[-/T/TT/TTT]GCAAACTAAGCATCT | 9873 |
rs200107454 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883854 | GGAGAATCGCTTGAG[-/C]CCAGGAGGTTCGGGC | 9873 |
rs200108232 | in-del | -/AAAAAAAAAAAAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845450 | CTCAAAAAAAAAAAA[-/AAAAAAAAAAAAC]AACAACAAACAAACA | 9873 |
rs200133588 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946547 | CTTAAAGTATAATTT[-/A]AAAAAAAACTAGACA | 9873 |
rs200153578 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851499 | TAATCCCAGCACTTT[C/G]GGAGGCCGAGGTGGG | 9873 |
rs200159157 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097615 | TTTTTTTTTTTTTTT[-/T]CTAATTACTGATTCA | 9873 |
rs200173029 | in-del | -/CA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871525 | GGTTAAGTAAGGTTC[-/CA]CTTACTTAACCTAAG | 9873 |
rs200198004 | in-del | -/ATA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890385 | AGTAAGAACAAAACA[-/ATA]TAATAACAGCAACAC | 9873 |
rs200234136 | in-del | -/TTA | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090761 | ATATAATGCATGTTT[-/TTA]TTGAGATGAAATTCA | 9873 |
rs200241574 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132824 | AATGAAACGGTAACA[A/G]AAAAAAAAAAAAAAA | 9873 |
rs200250879 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109396 | TGTCCTCTTCAATTT[A/C]TTTCATCAATGTTTT | 9873 |
rs200261651 | in-del | -/CTGT | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108082 | TGCCGGTGTTTGTTA[-/CTGT]CTGTCTTTTGGATAA | 9873 |
rs200269084 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978216 | ACCTAATGTAAATGA[C/T]GAGTTAATGGGTACA | 9873 |
rs200272080 | snp | A/T | 1.68071e-05 | 0.00289884 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72984133 | GTAGCGATCCTGATG[A/T]GCATTTGCTGCCGCT | 9873 |
rs200337344 | snp | A/C | 2.44807e-05 | 0.00349854 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838842 | TGCTGGCCTTCGGTG[A/C]TTCTGTGTAGGTGGA | 9873 |
rs200346955 | snp | C/T | 0.000129738 | 0.00805309 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921957 | ATCAAGAGCCTGTAA[C/T]AGAGGAGTAAATAAA | 9873 |
rs200370813 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067120 | CTGGATAAAGAAAAT[A/G]TGGCACATATACACC | 9873 |
rs200377316 | snp | C/T | 0.00299557 | 0.0385851 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842777 | ACGGATTATTGCTCC[C/T]TCAGGAAAAGATAAC | 9873 |
rs200382288 | in-del | -/AA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861396 | TATTTAAAAACTTCC[-/AA]AAAAAAAAAAAAACT | 9873 |
rs200382897 | in-del | -/AG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129703 | CAATAAATGTAATGC[-/AG]ACTTGAATCATCCCA | 9873 |
rs200391084 | snp | C/T | 0.000115318 | 0.00759249 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842750 | ATCATCTTGGTTTTC[C/T]TTGTTCAAGATACGG | 9873 |
rs200395290 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026837 | AATGGTTTAAAAGTT[C/T]GGCACTTCCCCCTTT | 9873 |
rs200419528 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106423 | AAAAAAAAAAAAAAA[C/T]AAAAAGAAAAAAGAA | 9873 |
rs200439027 | in-del | -/TGTA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035204 | GTATGTATGTATGTA[-/TGTA]CGTACTAAGACAAGG | 9873 |
rs200462571 | in-del | -/GAGA | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985678 | TATTCTGAACTTACT[-/GAGA]AAGTCCTGGGACTCT | 9873 |
rs200464991 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935353 | TCTTCAGCAATAAAG[A/T]TTTGCTGAAATCTCT | 9873 |
rs200475196 | snp | C/T | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143772 | CCACATGACCAGAAA[C/T]TGAAAAGGTGGAACT | 9873 |
rs200477185 | in-del | -/TATG | 0.129873 | 0.219248 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025993 | TATAGAGATTCATTT[-/TATG]TATGTATGTATGTAT | 9873 |
rs200499779 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891427 | GCAAAATAATCAATA[C/T]TCAAACTTAACCATC | 9873 |
rs200508014 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941468 | TTAGTATAAAATATA[-/G]ACTCCCAACTCTATT | 9873 |
rs200510857 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890391 | AACAAAACAATATAA[-/T]AACAGCAACACAATC | 9873 |
rs200513826 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024164 | TAATATACGTAAATT[-/A]AAAAAAAATCTACCA | 9873 |
rs200538165 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907602 | TAATCACGTGGGTTT[-/G]TTTTTTTTTTTTTTT | 9873 |
rs200561815 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979902 | CAAAAGACAGTCATA[A/G]TGAGGGTTGTTATCA | 9873 |
rs200567071 | in-del | -/GCA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910066 | GAGCACCTCTGCCCG[-/GCA]GCCGCCCCATCTGGG | 9873 |
rs200571034 | in-del | -/CA | 0.0225045 | 0.103662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035692 | CAGTACTGAAATGTT[-/CA]GTTTTTATTTATTTA | 9873 |
rs200584717 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014880 | CTGGAGTCTCACTCT[G/T]TCGCCCAGGCTGGAG | 9873 |
rs200589229 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950593 | AGACTATTCTTTCCT[-/C]CCACTGAATTGTTTT | 9873 |
rs200590736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886084 | CTCAAAACCTCTGGA[A/G]TTCTAAGGGGGTGTT | 9873 |
rs200623024 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866259 | ACTCTGTTCTGTTTT[G/T]TGTTTTGTTTTGTTT | 9873 |
rs200625859 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923160 | GTTGTACCACATTTT[A/G]TTTATTAATCAGGTG | 9873 |
rs200661196 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901865 | TTAATTCTATTCTGG[-/T]TTTTTTTTTTGTTTG | 9873 |
rs200661604 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907497 | ACTCTTATTATTTTG[A/C]GATATGTTCCAACAA | 9873 |
rs200684861 | snp | C/T | 0.00178316 | 0.0298061 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843114 | ACAGTTTAGGTCAAA[C/T]GTGACCAAATAAAGA | 9873 |
rs200687115 | snp | C/T | 0.00028187 | 0.0118683 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840916 | CTCAGGAGTATGCCT[C/T]GATGCCTGTGAGAAT | 9873 |
rs200720258 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968387 | TTTGTTCAGAAACGG[C/T]TACTCCTCTCCAGAG | 9873 |
rs200725859 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906201 | GATGAGCATTTTTTC[A/G]TGTCTGTTGGCTGCA | 9873 |
rs200728959 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110011 | TTTGCATATGTTGAA[A/C]CATCCTTGCATCCCT | 9873 |
rs200735136 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064487 | CTTCAAAAAAAAAAA[-/A]TCAATGAATCCAGGA | 9873 |
rs200737760 | in-del | -/T | 0.0170251 | 0.090679 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097510 | TTCCCTTTTCTTCTG[-/T]TTTTTTTGGAATAGT | 9873 |
rs200753128 | snp | A/G | 0.000131955 | 0.00812157 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72988978 | CTTTGCCTCGATGTC[A/G]GCTTTCTCTCGTACT | 9873 |
rs200761582 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057880 | TGCCAATTCGGTATT[C/T]TTTTTTTTTTTTTTT | 9873 |
rs200768834 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087719 | AAAAAAAAAAAAAAA[-/T]ATTTTTAAAATAAAT | 9873 |
rs200774518 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853505 | CTGCAACCTCCGCCT[C/G]CCAGGTTCAAGCAAT | 9873 |
rs200783836 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837813 | TAGCAGTTGGTCTGG[A/C]CCAGCCACAGCCTGG | 9873 |
rs200788964 | in-del | -/T/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907598 | GAGATAATCACGTGG[-/T/TT]GTTTTTTTTTTTTTT | 9873 |
rs200809431 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925058 | AGGCATCATGAGCTC[-/A]AAAAAAAAATAAGGC | 9873 |
rs200814557 | in-del | -/AA | 0.0119091 | 0.0762411 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086207 | TGAGGCCAGGAGTTT[-/AA]GACAGGCCTGGCCAA | 9873 |
rs200837586 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873329 | GTGAGACTCTGTTTC[-/A]AAAAAAAAAAAAAAT | 9873 |
rs200855476 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924680 | GCTGTTCCATTAAAC[-/T]TTTTTTTTTTTTTTT | 9873 |
rs200902127 | snp | C/T | 0.00299544 | 0.0385843 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843222 | GACGTGTGTGACCGA[C/T]TGTCCAAAGCGGCCA | 9873 |
rs200915587 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006057 | GGCCTACAGGCATGA[C/G]CCACTGCATGTGGCT | 9873 |
rs200960351 | in-del | -/ACTC | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033654 | CTATGTTAATTAAAT[-/ACTC]AAACTATGGAATTCT | 9873 |
rs200962772 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926195 | GGAGGGCCTGAAGAC[A/C]GGGGGCTGGACTGCC | 9873 |
rs200980735 | in-del | -/A | 0.0232847 | 0.105357 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142589 | AGGTGTAGAAACGCC[-/A]AGCGCCACGCGAAAA | 9873 |
rs201009553 | snp | A/C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105438 | TCTTTATTTGGTAAC[A/C/T]TTACTTTCCTAGGGA | 9873 |
rs201018083 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962612 | CCCCCTTTTTTTTTT[A/T]AACTAAGAATGTTCT | 9873 |
rs201055524 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085718 | AACTTTTTAACTATT[-/A]AAAAAAAAAATCCCT | 9873 |
rs201063455 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890391 | AACAAAACAATATAA[C/T]AACAGCAACACAATC | 9873 |
rs201093762 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947326 | GGCCCACATCTGGCC[-/A]AGAGGAGCAGAACTG | 9873 |
rs201145516 | in-del | -/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841383 | ATGCAGTTTTTTTTT[-/T]GCCCTTCAGGCGAAT | 9873 |
rs201157171 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109405 | CAATTTCTTTCATCA[A/G]TGTTTTATAGTTTTC | 9873 |
rs201158355 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003665 | CTAATTTTTTGTATT[C/T]TTAGTAGAGACGGGG | 9873 |
rs201229145 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995536 | TGAAACCTCATCTCT[-/A]AAAAAAAAAGTACAA | 9873 |
rs201245908 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992099 | TGCAAAAAATCACAA[A/G]CATTCTTATACACCA | 9873 |
rs201269620 | snp | A/G | 0.000341785 | 0.0130681 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841455 | AGGAGAACCCTTACC[A/G]TTTGCTGAAGGAGAC | 9873 |
rs201284616 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72984116 | ACTAAATCTGTTTGA[C/T]AGTAGCGATCCTGAT | 9873 |
rs201292605 | in-del | -/TTTTTTGTATC | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885208 | ATTTTACTTAGGCTA[-/TTTTTTGTATC]TGTTAAGTGGAAACC | 9873 |
rs201295990 | in-del | -/GAA | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900031 | TCCAGCACACCTGTT[-/GAA]GAAGATTAAGGTGCT | 9873 |
rs201296902 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065388 | ATTTATGACAAACCC[A/C]CAGCCAATATCATAC | 9873 |
rs201298041 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965048 | CCCGCCTTGGCCTCC[A/C]AAAGTGCTGGGATTA | 9873 |
rs201300387 | in-del | -/TTTA | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097373 | GTTTGTTTGGTTTAT[-/TTTA]TTTATTTATTTTTTT | 9873 |
rs201315056 | snp | A/G | 0.000224052 | 0.0105819 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72902570 | ACAAGGCTGGAACTG[A/G]AAGGGCTGGGGTTTG | 9873 |
rs201318726 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117149 | ATAAGCTGGTACTTA[C/T]AACAAATACATTCTA | 9873 |
rs201339205 | in-del | -/GGC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975759 | TGCCATACAGAAAGA[-/GGC]TGTTTATCTTTTATT | 9873 |
rs201356134 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100877 | GATTTTTTTTTTTTT[C/T]CTTAATGCTGTTTAG | 9873 |
rs201357306 | in-del | -/T | 0.0232847 | 0.105357 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041587 | GGATAATTTATGGAG[-/T]TTTTTTTGTTTGTTT | 9873 |
rs201364368 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080320 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA | 9873 |
rs201371746 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921085 | GACAAAAAAAAAAAA[-/A]TTGAACTGGATCTTT | 9873 |
rs201374616 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920068 | TATAGGATCTAAATA[A/G]AAAAAGAAGCTTGAG | 9873 |
rs201376447 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016149 | CTCTACCAAAAATAC[-/A]AAAATTAGCCGGGTG | 9873 |
rs201405233 | in-del | -/TTTG | 0.0391387 | 0.134304 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041604 | TTTTTTGTTTGTTTG[-/TTTG]CTACTGAGTTGAGTT | 9873 |
rs201459401 | in-del | -/TTTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035695 | TACTGAAATGTTCAG[-/TTTT]TATTTATTTATTTAT | 9873 |
rs201464402 | in-del | -/AA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908338 | AATAGTGCTGCAATC[-/AA]CATGAGAGTGCAGAT | 9873 |
rs201465503 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989418 | ACTGTTGGAGATATC[-/A]ATGATAATAAAATCA | 9873 |
rs201473940 | in-del | -/CG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049726 | GAAAGAGAGACACCT[-/CG]GAAGAGTTGGATAAT | 9873 |
rs201512091 | in-del | -/CAAA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855314 | AAACAAACAAACAAA[-/CAAA]AAAGACCAAAAAGTT | 9873 |
rs201515010 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902068 | TTAGTAGAGACAGGG[-/TT]TTGTCATGTTGGCCA | 9873 |
rs201565404 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906832 | GTTACTGTAGCCTTG[C/T]AGTATAGTTTGAAGT | 9873 |
rs201579323 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116960 | TTTCCCCAAAAAAAA[-/T]CACTATTGTTATATC | 9873 |
rs201596756 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866261 | TCTGTTCTGTTTTTT[G/T]TTTTGTTTTGTTTTT | 9873 |
rs201598501 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985609 | ATTATTTCCACCATT[A/G]AAAGTACTTCTTGTT | 9873 |
rs201613221 | snp | A/G | 0.000321982 | 0.0126841 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842846 | CACAAAACATACTAG[A/G]GAGCAAGAGAAAAAC | 9873 |
rs201618443 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866744 | CCTTTTTAAATGTGC[-/A]AGTGTATTCTCATTA | 9873 |
rs201620143 | snp | A/G | 0.000229183 | 0.0107023 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000965 | GATATTAAAATGCAT[A/G]TAAGAACAGAAATAA | 9873 |
rs201627189 | snp | C/T | 8.50593e-05 | 0.00652092 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985050 | TGTGAAATACACTTA[C/T]TGAAAACTTACCTTT | 9873 |
rs201639046 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913821 | AAAAACCAAAAAAAA[-/C]CCCAAAAAAAAAACA | 9873 |
rs201655074 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992384 | ATCAAGCTACCAATG[A/C]CTTTCTTCACAGAAT | 9873 |
rs201660154 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924696 | TTTTTTTTTTTTTTT[-/T]AAATACACAAATTCT | 9873 |
rs201676944 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109378 | TATCTTTCCATTTGT[C/T]TGTGTCCTCTTCAAT | 9873 |
rs201682261 | snp | C/T | 1.65803e-05 | 0.00287922 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840911 | GAGGTCTCAGGAGTA[C/T]GCCTTGATGCCTGTG | 9873 |
rs201721901 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900687 | GATTAAAAAAAAAAA[C/T]CACTACTATAAAGGG | 9873 |
rs201725751 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991338 | ATCAATAGAAAAAGA[C/G]GGAATCCTCCCTAAC | 9873 |
rs201734419 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109343 | AACAATATTGATTCT[C/T]CCAATCCATGAACAT | 9873 |
rs201739186 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016168 | ATTAGCCGGGTGTGG[G/T]AGCATGCGCCTGTAG | 9873 |
rs201755122 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967698 | GAGATAGTGGTGATG[A/G/T]TTGTACAACCTAGTA | 9873 |
rs201756436 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120820 | CTCACAGTCTGGAGG[G/T]GAAGATATACCAAAA | 9873 |
rs201765729 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103222 | CTCTGTACACTTAAG[C/T]TAGATGGATTTTATT | 9873 |
rs201774717 | in-del | -/ATTTCT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097671 | CACTTGTTATTGAGA[-/ATTTCT]ATTTTTTTCTGTAAT | 9873 |
rs201775859 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071535 | TTTCTACTAAAAATA[-/C]AAAAAAAAAAAAAAA | 9873 |
rs201783308 | in-del | -/A | 0.281313 | 0.248031 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928841 | TCGTCATTTAGCATT[-/A]AGGTATATCTCCTAA | 9873 |
rs201791287 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960572 | CATAATACTTCTTGG[C/T]CCAGTGTTCCATGCA | 9873 |
rs201795040 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892622 | TGTTTTTTGTTTTTT[-/T]GAGACAGAGTCTCAC | 9873 |
rs201818849 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097396 | TTATTTTTTTTTTTT[-/T]GCATCTCTCTTCACA | 9873 |
rs201841322 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082151 | GACCATCCTGGCCAA[A/C]AGGGTGAAACCCAGT | 9873 |
rs201858110 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896614 | TGGAATAAGTAGAAC[A/G]AAAGTCCCAAGGGAC | 9873 |
rs201864880 | snp | A/C/G | 0.00819378 | 0.0634803 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947756 | AAAACATAATTTTCT[A/C/G]ATAAAGAAAATTAAA | 9873 |
rs201865960 | snp | C/G | 0.000214145 | 0.0103454 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72849810 | CTTAAGGTGCCAGAA[C/G]GGCTGGAACTGCTGT | 9873 |
rs201894941 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943830 | GTTAGCACATCTATA[A/C]TTAAATATTTGTTCT | 9873 |
rs201895006 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883949 | AAAAAAAAAAAAAAA[A/T]TTTTTTTTAATGAGG | 9873 |
rs201906618 | in-del | -/TA | 0.0448719 | 0.142907 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025277 | ATAAAGAAAATGTGG[-/TA]TATATATATACCATG | 9873 |
rs201914151 | in-del | -/TAAA | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882715 | AGGAAACAGAGTGCC[-/TAAA]TAAATAGAGAGACAC | 9873 |
rs201946674 | snp | C/T | 2.78765e-05 | 0.00373329 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015915 | ATATTTTTTCTAAAA[C/T]AAATATTATGCCATA | 9873 |
rs201952781 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086263 | AAAATACAAAAATTA[G/T]CTGGGCGTGGTGGTG | 9873 |
rs201956100 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978176 | TGGGGTGGGGGGAGC[A/G]GGGAGGGATAGCGTT | 9873 |
rs201970337 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946041 | CCCAGCCATTCCATT[A/T]CCGAGTATATACTCA | 9873 |
rs201980141 | in-del | -/GTATGTAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035198 | TATGTATGTATGTAT[-/GTATGTAC]GTACTAAGACAAGGT | 9873 |
rs201980904 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907620 | TTTTTTTTTTTTTTT[C/T]TTGAGACGGAGTCTG | 9873 |
rs202001987 | in-del | -/TGAATGCTT | 0.0341408 | 0.126114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907442 | GCTTCCAGTTTTTGC[-/TGAATGCTT]CCATTCAGTATAATA | 9873 |
rs202043775 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973218 | ACTAAAAATACAAAA[G/T]TAGCTGGGTGTGGTG | 9873 |
rs202050835 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975897 | ATTAAATTGACGTTT[C/G]TTCTCTTTTCTACTA | 9873 |
rs202075634 | in-del | -/AA | 0.0356815 | 0.128715 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873074 | GTGGCTCATGCCTAT[-/AA]TCCCAGCACTTCGGG | 9873 |
rs202083118 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941481 | AGACTCCCAACTCTA[-/T]TTAATATATTACTTA | 9873 |
rs202108873 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116948 | AACCTTTCCATTTTT[-/C]CCCAAAAAAAATCAC | 9873 |
rs202109035 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017277 | AGTCACCAAACCTGG[-/C]CAACGTATTACTTTT | 9873 |
rs202112144 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100876 | GATTTTTTTTTTTTT[-/T]CCTTAATGCTGTTTA | 9873 |
rs202119912 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063047 | CAGAGAGAAAGGTCA[G/T]GTTACCCACAAAGGG | 9873 |
rs202144556 | snp | C/T | 4.98194e-05 | 0.00499071 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849910 | AAAAATTAGAAACCA[C/T]TGGCTAGTTTCCTTA | 9873 |
rs202178689 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840890 | ACAGGTCGCAGTTTG[C/T]CATATGAGGTCTCAG | 9873 |
rs202179623 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126336 | CAGGGCAAGATTCCA[A/T]CTTAAAAAAAAAAAA | 9873 |
rs202185212 | snp | C/T | 8.86486e-05 | 0.00665706 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902658 | AGAGAAAATAAAATA[C/T]CTTTAGGTCTTTAAT | 9873 |
rs202202871 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085914 | ATTCAAAGGGGAAAA[A/C]AAGCCAATACAAATT | 9873 |
rs202226782 | in-del | -/TTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851878 | ATCAGTCAGAGTGGC[-/TTT]TTTTTTTTTTTTTTG | 9873 |
rs207472005 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032357 | CCTCGGCTTCCCAAG[A/G]AACTAATATTACAGG | 9873 |
rs367550753 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066911 | TACTTCAACCATTGT[A/G]GAAGACAGTGTAGCG | 9873 |
rs367582930 | in-del | -/AGA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900036 | CACACCTGTTGAAGA[-/AGA]TTAAGGTGCTTCACA | 9873 |
rs367632709 | in-del | -/A/AA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132824 | ATGAAACGGTAACAG[-/A/AA]AAAAAAAAAAAAAAA | 9873 |
rs367639909 | snp | C/T | 3.48693e-05 | 0.00417534 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72889941 | TCTGATTCTAACTGT[C/T]GGCTCTACAATACAA | 9873 |
rs367666447 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992251 | CAAACCACTGCTCAA[G/T]GAAATAAAAGAGGAT | 9873 |
rs367683290 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924744 | TAATAAAGCTGCACC[G/T]TCTATAGTGCTTACA | 9873 |
rs367685476 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090110 | TTGTGTTGGGATAAC[C/T]TGATAGGAAGATCTA | 9873 |
rs367685737 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002431 | AACGAATGCTCTCCA[C/T]GGCCTCACTGCATGA | 9873 |
rs367689342 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112725 | ATGATCTCAGCTCAC[C/T]ACAACCTCTGCCTCC | 9873 |
rs367695555 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029090 | GACCAGAAAGGGCAC[C/G]ATAAATATAATGGTG | 9873 |
rs367695760 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000745 | ATTATGCCGAAAAGC[A/G]GTATTACTAAAAAGT | 9873 |
rs367699025 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130379 | CAAGGACTACAGGCA[C/T]GTGCTATGGTGCCAG | 9873 |
rs367701194 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099145 | CACCGAGCCCAGGCG[C/T]TCCAGGTTGCAGTAA | 9873 |
rs367734791 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123380 | ACAATGCATATTAAA[C/T]GGTGGTAACTCCTGG | 9873 |
rs367734833 | in-del | -/CCTTCTCATTC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096049 | AACAAAACAAAAAAA[-/CCTTCTCATTC]AAAAATAAACCACCA | 9873 |
rs367745075 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091715 | TTGGAATTTCCTCCC[A/G]TTATTTGGCCTAACT | 9873 |
rs367771000 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062318 | AAGGTACACAAATCC[A/G]CAAAGATGGGGAGAA | 9873 |
rs367780229 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917694 | AGTTCAAGACTAGCC[C/T]GGCTAACATGACGAA | 9873 |
rs367780871 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932064 | AGTTCCTCAGTGTGT[A/G]ATGCCACTATTCACT | 9873 |
rs367784456 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960768 | GGGCAAGGGACAGGG[A/C]ATAATAAAGAACCCC | 9873 |
rs367786674 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996235 | ACTCTGTTATTTACT[A/G]CCTAAGTCTCTTTAA | 9873 |
rs367801051 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017320 | ATGTGGTCCCCTAAC[A/G]CTATAACAGGGCCTA | 9873 |
rs367811851 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006187 | TCTGGGATTACATAC[A/G]TGAACCACTACTCTC | 9873 |
rs367816005 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956232 | AACAAGCACATAAAT[A/G]GCAGAGAATAGAAAC | 9873 |
rs367825165 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928393 | TGTTCTCTGCATTAT[A/G]CTCTACTTCCCAACT | 9873 |
rs367837031 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897124 | AGGCGTGAGCCACCA[C/T]GCCCGGCCGTCCTGT | 9873 |
rs367867112 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070557 | GCCTCCTGAGTAGCT[A/G]GTATTACAGGCGCCT | 9873 |
rs367872795 | in-del | -/TTCT | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111370 | CATTATACAATGACC[-/TTCT]TTGTCTCTTCTAAAA | 9873 |
rs367876577 | in-del | -/G | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143002 | CTACTCTCCCTACCA[-/G]CTAGATGTGCGCGAG | 9873 |
rs367886976 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870078 | TGCGTGCCTGTGTGC[A/G]TGCCAGTCCCTCTGT | 9873 |
rs367895469 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847771 | GATCTTGGCTCACTG[C/G]AACCTCCTCCTCCTG | 9873 |
rs367901975 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109731 | TAGGACTTCCAGTAA[C/T]ACACTGAGTAACAGT | 9873 |
rs367903852 | in-del | -/TG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931113 | TTTTTTTTTTTTTTT[-/TG]AAAAGGAGTCGCGCT | 9873 |
rs367905842 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934804 | ATATACTTAAAAAAA[C/T]AGCCAAACTTTTTGA | 9873 |
rs367915822 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917917 | AAAAAATTGAGGACC[A/G]GCTTTTCCATTTCTG | 9873 |
rs367926797 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861473 | GAAGACGAAATTCCA[C/T]ACAATTCTACACAAG | 9873 |
rs367927694 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947760 | CATAATTTTCTCATA[A/T]AGAAAATTAAATACA | 9873 |
rs367928077 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011345 | CTACCTTCTGAGCTG[-/G]AAGCCTAGGCTAGCA | 9873 |
rs367939016 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991142 | TCCTCGACACATACA[C/T]CCTCCCAAGACTAAA | 9873 |
rs367943180 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950715 | CTTTTAGGATATTTT[A/C]ATTTTTCATTTATAA | 9873 |
rs367964796 | in-del | -/C | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143967 | AGGGAAGGCCTGGGG[-/C]AAGGGGACAGGTGGA | 9873 |
rs368003593 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903845 | AGTAGTAGGTGTATA[C/T]TGCATTTTGTTTACC | 9873 |
rs368008403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870508 | TGCCATTCAATGATA[C/T]TGAGTTATAAACTAC | 9873 |
rs368008664 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943552 | TGAAAGGGAAGGAAA[C/T]TGAAGAGAATGACAG | 9873 |
rs368010371 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900316 | TATCCACCAGTTGGG[C/T]GGCTTTTAAACTCTG | 9873 |
rs368024554 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965475 | CTACTTCTATAAAGC[C/G]TTTTGTGACTTTCCT | 9873 |
rs368035510 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896398 | TTCCCATCCCAGCTT[C/T]GCTTTGTCCTTTTTC | 9873 |
rs368050578 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994688 | GGAGAATGGCTTGAA[C/T]CCAGGAGGTAGAGCT | 9873 |
rs368051476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001677 | CGCGGCTGGAAAAAT[A/G]TATCATGAACAACTG | 9873 |
rs368062555 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959811 | ATGCTGATGAGCAGA[A/G]GTAGAACTATACTTC | 9873 |
rs368085784 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944336 | CAGAAAAGGCCTTTG[A/G]CAAAATTCAACAACG | 9873 |
rs368106300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082607 | AAAGCCTAAAAGAGT[C/T]ATGCCCCAATCTCTC | 9873 |
rs368123466 | in-del | -/GA | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842252 | GCTCTGACAGTGAGG[-/GA]GAGAGAGAGCCAGCT | 9873 |
rs368134636 | snp | C/T | 0.000154888 | 0.00879886 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840858 | TGCATTCGATAATCC[C/T]GCAAGATCAGAGACT | 9873 |
rs368161429 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033904 | TTGAAACATGATGGT[A/G]AACAACGCTTATGAC | 9873 |
rs368191101 | in-del | -/TTTA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035697 | CTGAAATGTTCAGTT[-/TTTA]TTTATTTATTTATTT | 9873 |
rs368232959 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057277 | CCTAGGACACAGTAC[A/G]CAGGTTCGAAGCATG | 9873 |
rs368243277 | in-del | -/GC | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841365 | AAAAAAAAAAAAAAA[-/GC]AAATGCAGTTTTTTT | 9873 |
rs368246136 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973239 | GGGTGTGGTGGCATG[C/T]GCCTGTAATCCCAGC | 9873 |
rs368265647 | snp | C/T | 3.62457e-05 | 0.00425694 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843124 | TCAAACGTGACCAAA[C/T]AAAGAGTGCCTTGTT | 9873 |
rs368267125 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992785 | AAGACTTAAATGTTA[-/G]ACCTAAAACCATAAA | 9873 |
rs368271488 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107261 | GGTTTCACCATGTTG[C/G]CCAGGATAGTCGATC | 9873 |
rs368273321 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006656 | TTACAGCAATTGCTG[C/T]GCAATCACTTCTTGG | 9873 |
rs368296357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861817 | ATGCCTATAATCCCA[A/G]CTACTTGGGAGGCTG | 9873 |
rs368324915 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131256 | GGCGCAGTGGTTCAC[A/G]CCTGTAATCCCAGCA | 9873 |
rs368332938 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016147 | ATCTCTACCAAAAAT[A/G]CAAAAATTAGCCGGG | 9873 |
rs368333075 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877348 | AAGATGGAGGTTCTG[C/T]TTAAATTCTGGTTGT | 9873 |
rs368367894 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969600 | AATACAAGAAGCATC[A/G]AAGATATAAAAAACA | 9873 |
rs368402914 | snp | A/C | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143969 | GGAAGGCCTGGGGCA[A/C]GGGGACAGGTGGATG | 9873 |
rs368406708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084446 | CCTAGGCTTGAGTGC[A/G]GCGGTGAGGTCCTAG | 9873 |
rs368407877 | snp | G/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72887567 | TGACACTCCAGATCA[G/T]TTAGAACCTATTAAA | 9873 |
rs368418620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905849 | ATCATTGATGGACAT[C/T]TGGGTTGGCTCCAAG | 9873 |
rs368439520 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870867 | ATTGCGCCACTGCAC[A/T]ACAGCCTGGGTGACA | 9873 |
rs368443132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910300 | TTTGTCCGGCCGCCC[C/T]GTCTGGGAGGTGTAC | 9873 |
rs368448051 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988346 | TTGCTTTATATCACC[C/T]TCTATTACCAGTTGC | 9873 |
rs368454241 | snp | A/G | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840234 | TCATTTGGGATAAAG[A/G]CTCAAGTCCTTAAGA | 9873 |
rs368461314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057423 | TTACTGTGGTAATTA[C/T]GGGGGTTCCCAGCTT | 9873 |
rs368461885 | snp | A/C | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143495 | GCACCCCACCACCAC[A/C]CATGAACCTTCCTGC | 9873 |
rs368461952 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978425 | GCATATAAAAAGGTG[C/T]TCAATATCATTGACC | 9873 |
rs368463095 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898485 | TTCAAACTATAAAAT[A/T]CAAAATAAAAGAACA | 9873 |
rs368466459 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069858 | TTCATAAATGATACA[C/T]TGGTCTCATTCCACA | 9873 |
rs368475839 | in-del | -/AC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871526 | TTAAGTAAGGTTCCA[-/AC]CTTACTTAACCTAAG | 9873 |
rs368488720 | snp | A/G | 0.0015437 | 0.0277393 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868075 | CTTTTATTATTCACA[A/G]TAGCAAAGATAAGGA | 9873 |
rs368503360 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917185 | AGATGAGGTTTCACC[A/G]TATTGGCCAGGCTGG | 9873 |
rs368517276 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113327 | GGTACCTTAGTTTGG[C/T]TGATCATCATGCTTC | 9873 |
rs368528340 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868857 | TTGCACAACTGTATT[A/C]TTGGTGGCAATGCAG | 9873 |
rs368530743 | in-del | -/GTCTCAG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134481 | TCTCAAAAAAAAAAA[-/GTCTCAG]AACATCCATAAACAG | 9873 |
rs368541963 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123303 | TCCTGCAGTATCTCC[C/T]AGCCAAGCCAGTATT | 9873 |
rs368544385 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896890 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 9873 |
rs368549352 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931550 | GCAGGTGGATCACAA[-/C]GGTCAGGAGTTCAAG | 9873 |
rs368558079 | snp | C/T | 0.000167986 | 0.00916323 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985014 | CAATTCTCTGTTTTA[C/T]AAGCTAAGAGGTTTC | 9873 |
rs368565080 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962844 | AGATTACAGAACTGC[C/G]ACAAAAGTTAAATAT | 9873 |
rs368604322 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853375 | TAAGCCTATGAAACT[G/T]TAAAAGAAAACACAG | 9873 |
rs368608709 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984909 | GGGTGCAAAACCCCC[-/C]ATGAACTGGGAGGGA | 9873 |
rs368613716 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949345 | ATCACAGCTACTCAG[C/G]AGGCTGAGACAGGAG | 9873 |
rs368644886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108662 | CAAGCTCCGCTTCCC[A/G]GGTTCACGCCATTCT | 9873 |
rs368647135 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889542 | TGGCAAGACCCTATC[C/T]CTACAAAAAATCTAA | 9873 |
rs368659761 | snp | A/G | | | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72849840 | TCATCGAAAACATCC[A/G]TGTTATCTTCAAACT | 9873 |
rs368669408 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989689 | GGAGAAGGGATGGAC[A/C]TAACAACTAAAACAA | 9873 |
rs368677495 | snp | A/G | 4.99671e-05 | 0.00499811 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72889895 | TTTTCGAGCTTCCTT[A/G]TTTAGACTGTGCTCC | 9873 |
rs368696879 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997216 | GCAGCTACACGATGT[C/T]GAGAAGACAAAGGTT | 9873 |
rs368726413 | in-del | -/CC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004436 | CCTCCTGATTCTACT[-/CC]CAAACCCTTTAGAAT | 9873 |
rs368736333 | snp | A/G | 0.000199727 | 0.00999118 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841416 | GTAGGTTTCTGAAGT[A/G]AAAATGCATTTAGAC | 9873 |
rs368745203 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911114 | CTTTTAGTAGTTTCA[C/T]AGTTTGAGGTCTTAG | 9873 |
rs368746768 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929072 | ATTTTTTATGGCTGG[A/G]TAGTATTCCATGGTG | 9873 |
rs368763998 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132122 | TGAAGAGGCAATGAC[A/G]ACTGCATCACAGCCT | 9873 |
rs368765590 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119684 | ACTCCTGGCTTCAAG[C/T]GATCCTCCCACCTTG | 9873 |
rs368775478 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102438 | ACAAATGTGTACAAA[A/G]TGTGTACAGCAGCAT | 9873 |
rs368795801 | in-del | -/AGGA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966203 | TCACTCTGTCGCCCA[-/AGGA]GGAAGGAGTGCAGTG | 9873 |
rs368803817 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094473 | ACAAAAATATTTATA[A/C]CATCTTTAGTCATAA | 9873 |
rs368859921 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968299 | CTTAAGACTGATAGA[C/T]CTTTGCCTTTTAATT | 9873 |
rs368864043 | in-del | -/AA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076958 | CTCTACTAAAAATAC[-/AA]AAAAAATTAGCCAGG | 9873 |
rs368880489 | snp | A/C/T | 0.000356943 | 0.0133553 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73001048 | GGCTCAGAAATGAAG[A/C/T]TTTTATAGTTTTCAC | 9873 |
rs368911084 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054382 | CAGACAGGGGGCTAG[-/A]AAAAAAAAAGAAATT | 9873 |
rs368911938 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907540 | TGAGAGTTTTTAGCA[C/T]GAAGGGCTGCTAAAT | 9873 |
rs368915774 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885470 | AGTCTAGTTTGGCAT[A/G]CTATGGAAATAATAG | 9873 |
rs368915914 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077444 | AGCACCTAGAACTCA[A/C]ATACACAGCTGGTGG | 9873 |
rs368935748 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938815 | CTTATCAAGCTAACC[C/T]AAGACTAATTTATCA | 9873 |
rs368938666 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096419 | AGCCAGATGTGGTGG[C/T]GGGCGCCTGTAATTC | 9873 |
rs368967084 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874742 | TTAGACTGCAGTCCC[A/G]GAATTAAACACTGCT | 9873 |
rs368981030 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873202 | GACACGGTGGCGGGT[A/G]CCTGTAATCCCAGCT | 9873 |
rs368983956 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966615 | TGATGCAAACAGATT[C/G]CTGCATGAATACATT | 9873 |
rs368984181 | in-del | -/GA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885240 | TGGAAACCAAGWGAG[-/GA]AKTATTTTATGCTAA | 9873 |
rs368989172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006330 | CAAAACTAAATTCTT[C/G]ATTTCCCTAAAATCT | 9873 |
rs368995456 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929298 | CTGAGGAATAGAAGC[C/T]ACTTTCAATGGAGAT | 9873 |
rs369015175 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029817 | TTAGTAAGTCACCAC[A/T]ATATACAGAGAAAGG | 9873 |
rs369020177 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879906 | TGAGAGACTGAGGCC[A/G]AACAATCGGTTGAAC | 9873 |
rs369020667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078512 | AACTACTACTACATG[C/T]AACAACATGCATGAA | 9873 |
rs369023201 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043274 | TGAAGGAATTTTTAC[-/T]TCTCTTCATCACAGA | 9873 |
rs369024565 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884354 | TTCTGTATGTTTGAA[A/C]ATTTTCAGTAAAAAA | 9873 |
rs369032350 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854854 | AAAGAATACTAGAAA[C/T]GGGCCAGGCACGGTG | 9873 |
rs369033136 | in-del | -/ATG | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118701 | ATGTGATCAGAGAAT[-/ATG]ATGATACTATAATGA | 9873 |
rs369033928 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907814 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 9873 |
rs369035653 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894269 | ATATACTGGGGCTGG[A/G]CACAGTAGCTCACAC | 9873 |
rs369038418 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981061 | TCAATGGTGGAAATT[C/T]ACTAAGTAGCTAACA | 9873 |
rs369044485 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030571 | AGGTCTCTTACCTGA[C/T]GACCTTAACTTTGTA | 9873 |
rs369046018 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998868 | CCTTGTGCACTGTTG[A/G]TGGGAATGCCAAATG | 9873 |
rs369049901 | in-del | -/TCTTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888650 | GGAGACAGGGTCTTT[-/TCTTT]CTCTGTCACCCAGTC | 9873 |
rs369060852 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992603 | CTCAGAAATAATGCC[A/G]CATATCTACAACTAT | 9873 |
rs369071419 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132234 | AACTTCCTTTTGTAC[A/C]TTGAATAAGACAACA | 9873 |
rs369077477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050532 | AATAGTTCCTTTCGT[A/G]GGACAACATTGGAGT | 9873 |
rs369082709 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931749 | TAGTCTGGGTGACAG[A/G]GCAAGACCCTGTCTC | 9873 |
rs369095699 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873023 | TTTGCATTTTCCTGG[A/G]TAACTATTAATGTTA | 9873 |
rs369095812 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864785 | TTGTCATCTTGGTAT[A/G]GCTTTTGAATAAGAG | 9873 |
rs369135921 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035246 | CACCCAGGTTGGAGC[A/G]CAGTGGCGCGATCTT | 9873 |
rs369144556 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048970 | AGAGCTATGAAGAAC[A/G]GTAAATATTTAAATA | 9873 |
rs369175013 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108818 | CCTCATGATCCACCC[A/G]CTTCGGCCTCCCAAA | 9873 |
rs369185909 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043335 | GAAGATAAATATTAT[A/C]AGTTTCCATAAGCAA | 9873 |
rs369207284 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906138 | CATTCTGTTGTGACA[C/T]AGTATCTCATTGTGG | 9873 |
rs369215343 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036862 | ACAATTTTCTGTAAT[A/G]CACATATTCTGCTTA | 9873 |
rs369215706 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039249 | TTCTGCAGGGTGCAG[G/T]GCTCACACCTGTAAG | 9873 |
rs369219061 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871888 | TGAACTGCTGTGCCC[A/C]ACAGGTACATAATTT | 9873 |
rs369263755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901083 | TCAAGGACGATTACT[C/G]TATGCTTTTAAACAA | 9873 |
rs369274428 | in-del | -/TTAAGTAAGGTTCC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871512 | TAAGCTAATTTTAGG[-/TTAAGTAAGGTTCC]ACTTACTTAACCTAA | 9873 |
rs369285667 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004439 | TCCTGATTCTACTCA[A/G]ACCCTTTAGAATTCT | 9873 |
rs369289700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930442 | AGAGATTCATCTCTA[C/T]ATTTTCTTTGACTTC | 9873 |
rs369295273 | snp | C/T | 4.63639e-05 | 0.00481454 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72921877 | TTCTGCACAGCTTGG[C/T]ATGTTTCTAGCTCAG | 9873 |
rs369300695 | snp | C/T | 8.24205e-05 | 0.00641899 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843376 | CACACACAATTTAGA[C/T]AGGGCACAACAAAGA | 9873 |
rs369303085 | snp | C/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842367 | GTATGTCACATATAA[C/T]TTGGCATTTTGGTTA | 9873 |
rs369305227 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004182 | TCTACATATCACATG[A/G]TAAGTACTACGTTAT | 9873 |
rs369313444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858148 | AGAATCTGGTAATAC[C/T]TAATACAGAGGAAGA | 9873 |
rs369313931 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006196 | ACATACATGAACCAC[C/T]ACTCTCAGCCCAATT | 9873 |
rs369315223 | snp | A/T | 0.000268276 | 0.0115787 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841497 | CAGGGAGCTCCTCTT[A/T]TCTGGGCTGGGGTAG | 9873 |
rs369316091 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051856 | ACCTTCAGGATGCTA[A/C]CACGGTATATAAACA | 9873 |
rs369322682 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016396 | ACACTACAACCTTTT[C/T]TCATTATTGTCCAGT | 9873 |
rs369344558 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983085 | GGATCACGAGGTCAG[C/G]AGATCGAGACCATCC | 9873 |
rs369363765 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937388 | ATCAAAGTATTGAAC[C/T]GACAGAAAGCATTTA | 9873 |
rs369393504 | snp | A/C | 0.000629822 | 0.0177346 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902498 | GTTACTTAAGCACAA[A/C]CACAACTGAACAACA | 9873 |
rs369415482 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118365 | AATGGCACTATCATC[C/G]CAAAAAGTTTCCTCA | 9873 |
rs369441390 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997507 | ATAACCAAAAATCAA[C/G]AAAAACCGCAGGCGG | 9873 |
rs369449969 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937748 | AGAACCTGGGCAAGC[A/G]TTGGAAACAAACAAA | 9873 |
rs369458748 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071566 | ATTAGCTGGGCATGG[G/T]GGTGTGTGCCCGTAG | 9873 |
rs369468492 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843427 | TGTCACAAGAAAGGG[C/T]GATATGAGCAAAGGA | 9873 |
rs369497265 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079354 | GGTACCCGCCACGAC[A/G]CCTGGCTAATTTTTT | 9873 |
rs369507203 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044053 | AAACAATTAGCCTAT[C/G]CAAATGAACACAGTA | 9873 |
rs369513274 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010746 | AGGACTGGGGCACCA[A/G]GTAGGCCAGTCTTTG | 9873 |
rs369537734 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019115 | CATCTAAATGACATG[A/G]TAGTGACTTTTTCAG | 9873 |
rs369546889 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73141935 | AAGGACCAGGAGGAG[A/G]AGGAGGGCCGGAGAG | 9873 |
rs369552692 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899950 | TACCGTATGACTCTG[A/G]ACAAGTCTCCCTTAC | 9873 |
rs369559627 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040758 | ATGTATTCTAATTAT[G/T]TTGAAAGACATATTG | 9873 |
rs369562211 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124193 | CATGTTCTCACTCAT[A/G]GATGGGAATTGAACA | 9873 |
rs369593900 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096730 | ACTGTGAGCTTGTCA[C/T]ATGTGCCCTTTAACA | 9873 |
rs369608429 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052142 | TTTCCTTTGGTATAT[A/C]TGTGATCTGAACATG | 9873 |
rs369614111 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101365 | ATCTAAGTTCAGAGA[A/G]AGGAGTGATAACTCT | 9873 |
rs369617685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908530 | CCCTTTTCTCCACAT[C/T]CTCACCAGCATCTGT | 9873 |
rs369620863 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069169 | TACAAAAATTAGCCA[G/T]GCGTGGTGGCATGCA | 9873 |
rs369627062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019730 | ACTCTGGGGCTATTA[C/T]AGTAAAGGTCCTAAA | 9873 |
rs369636857 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072302 | TACGAGATGTGCTAC[C/T]GAATAGCCATGAAAA | 9873 |
rs369639708 | in-del | -/AT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887077 | TCCTAAGCTCTGAAA[-/AT]ATATATATATATATG | 9873 |
rs369649475 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992479 | AAAAGAACAAAGCTG[C/G]AGGCATCACACTACC | 9873 |
rs369674043 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901291 | GGCCCCAGCTAATCG[G/T]GAGGCTGATGTGGGA | 9873 |
rs369695601 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945659 | TACTCATCTGACAAA[C/G]GGCTAATATCTAGAA | 9873 |
rs369700486 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066821 | TGGCGATCATTAAAA[A/G]GTCAGGAAACAACAG | 9873 |
rs369705103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949567 | GCCTGGCAACCACTA[A/G]TCTACTTTCTACATT | 9873 |
rs369711968 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104480 | TCACCATGTTGGCCA[C/G]GGTGGTCTCAAACTC | 9873 |
rs369713004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124177 | AGAAAACCAAACACC[A/G]CATGTTCTCACTCAT | 9873 |
rs369718040 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017958 | ATCCCTCATGAACTA[C/T]CTGGTTATATTGAGA | 9873 |
rs369720865 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065539 | AAGAAATAAAAGGTA[C/T]TCAAATAGGAAGAGA | 9873 |
rs369749417 | in-del | -/AACAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106632 | TAAATACAGTAACAT[-/AACAT]TTCCATAAAAAATGG | 9873 |
rs369765858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914514 | GGCCACAGCAACCAA[A/G]CAGCATGGTACTAGT | 9873 |
rs369766908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028502 | TTGATTTTACAGGCT[C/T]ACAGGCAGAAGGGAC | 9873 |
rs369773160 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915277 | TTGTGGAGAAAAAGG[A/C]ACACTTTTACACTGT | 9873 |
rs369794395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116996 | TTCATTTTTAGCATA[C/T]TGATTTTTATTACTC | 9873 |
rs369813919 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855348 | GGGTGTGGTGGCAGG[G/T]GCCTGTAATCCCAGC | 9873 |
rs369816755 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855475 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAGAGTT | 9873 |
rs369827007 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094177 | GACCACGCCAATGCA[C/T]TCCAGCCTGGGCTAC | 9873 |
rs369829973 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893748 | GGAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAC | 9873 |
rs369839004 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029924 | TAATCAAAAACAAAA[C/G]AAAAACAAAAACAAA | 9873 |
rs369841182 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048020 | CTATATTGTTTCTTT[-/T]AAGTAGTACATACTG | 9873 |
rs369861585 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892663 | AGGCTGGAGTGCAGT[A/G]GCATGATCTCAGCTC | 9873 |
rs369874613 | in-del | -/TATATATAAGATCATATATATAGTTTA | 0.0138799 | 0.0821421 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884531 | TAATCATACATAGTT[-/TATATATAAGATCATATATATAGTTTA]TATATATGATGATAT | 9873 |
rs369887017 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954079 | TGGCTATTACGCAGA[A/G]AATAGACATAAAGGT | 9873 |
rs369899455 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986187 | TTTTTTACCTTGTCA[C/T]AGTCATATTTCATAA | 9873 |
rs369930628 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866149 | AAGTGGGCCTGGAAT[G/T]TGCTGTCATCAAAAA | 9873 |
rs369934177 | snp | A/G | 1.93646e-05 | 0.00311158 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73001053 | AGAAATGAAGTTTTT[A/G]TAGTTTTCACATATA | 9873 |
rs369941149 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973913 | CTATTTATTATCTGT[C/T]CCTTTACAAGAAATG | 9873 |
rs369948122 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074090 | CAGTGTGATATCGGG[-/A]AAAAAATATTTCAAA | 9873 |
rs369961395 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069310 | GCAAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 9873 |
rs369975719 | snp | A/C/G | 3.29491e-05 | 0.00405877 | missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843247 | CGGCCAGGGACTGCA[A/C/G]CATGCTCAGGAGGCT | 9873 |
rs369985163 | in-del | -/TG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958994 | CTCATCAGTAAGATA[-/TG]TGTGTGTGTGTGTGT | 9873 |
rs370003615 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886485 | CTTCAACTATACTTA[A/G]TGCACCACTCCTCGG | 9873 |
rs370014040 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125024 | GACCAACTCAGAATT[C/G]TATATCCAGCAAAAA | 9873 |
rs370021960 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029408 | ACTCCCAGAGAAAGA[C/T]TTGGAGAGTAAATTA | 9873 |
rs370022558 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043069 | TTGACTGATGCTCTG[G/T]CTAGAACTTCTGCCA | 9873 |
rs370065778 | snp | C/T | 0.000131898 | 0.00811982 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842612 | TCAACTGTCTCCCCT[C/T]TCAGGTACCTGAATC | 9873 |
rs370068827 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875394 | ATTTGACAGAGTCTC[A/G]CTCTGCTGCCCAGGC | 9873 |
rs370091016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005993 | GCTTACTACAGCCTC[A/G]AACCCCTGGACTCAA | 9873 |
rs370098964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098394 | CTAGCTTCATTCCTC[C/T]ATGGGTAAAGAAAAT | 9873 |
rs370113610 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888603 | AGTCTTCGAGATATA[C/T]TTTCTTTCTTTCTTT | 9873 |
rs370119525 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861754 | GACCGACATAGAGAA[A/C]CCCTATCTCTACTAA | 9873 |
rs370143460 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956602 | GTGTCTGGTGAGGGC[C/T]CACTTCCTGGATCAT | 9873 |
rs370152940 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089196 | ATAATCTCCATGTAA[C/G]ATGAAAAGGCATTTG | 9873 |
rs370154472 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118757 | CTTACCACGTGTAAT[A/G]CATTGTTCTGAATGC | 9873 |
rs370191845 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936878 | TCTTTGAAATATATT[A/T]AAAATAGGCGATTTA | 9873 |
rs370218294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943440 | AAGGATTAGTGAGAC[A/G]CTGAATCAGGAAAAA | 9873 |
rs370218807 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001961 | CTAGCATGCTCCTAC[A/G]CTATTTATAAACACA | 9873 |
rs370226557 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909841 | CTCTGCCCGGCAGCC[A/G]CCCCATCTGGGAAGT | 9873 |
rs370246364 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088289 | TACAGTAACATGTTG[C/T]ACAGGTTTGTAGCCT | 9873 |
rs370251087 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076454 | AAGAAAGGAGACATA[C/G]CATATGATTACATTT | 9873 |
rs370251322 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977479 | TAAGGAGCTCAAACA[A/G]CTCTATAGGAAAAAA | 9873 |
rs370262297 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128534 | AATTTCTGGTAAAAA[-/A]TTTCTTCCCTGGTGG | 9873 |
rs370271176 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067312 | TAGGGAGGGGAATAT[A/C]ACACACCAGGGCCTG | 9873 |
rs370273285 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934224 | TCTGTATCTTGTCTA[G/T]CATTTTACATTTAAA | 9873 |
rs370276042 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881626 | CAGTGGCCAAGATGT[A/G]GAATCAACCTAAGTG | 9873 |
rs370292311 | in-del | -/ACACACACACAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051869 | TAACACGGTATATAA[-/ACACACACACAC]ACACACACACACACA | 9873 |
rs370292718 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142046 | CGGGCGGCAGGCGGA[C/T]CCCAGCCAGAGAGCG | 9873 |
rs370311064 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013288 | GGGTTATTTTCACTT[A/C]GAATTTCTTTTACCA | 9873 |
rs370324130 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896399 | TCCCATCCCAGCTTC[A/G]CTTTGTCCTTTTTCA | 9873 |
rs370333227 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992816 | AACCCTAGAAGAAAA[C/G]CTAGGCAATACCATT | 9873 |
rs370339159 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054969 | CATACTTGAGACTGG[A/G]TAGTTTATAAAAAGA | 9873 |
rs370342500 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948370 | ACTTCAAAATTACTG[A/G]ATGTTTCATTTTTCA | 9873 |
rs370345537 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038660 | TTGAATACAAATGGA[C/G]ATAAACATGGGAATA | 9873 |
rs370352416 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916027 | ATTATGAGAACACAT[A/G]GGAACAACGCACACT | 9873 |
rs370353231 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082075 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 9873 |
rs370357373 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866472 | ACAGCGTTTCACCAT[C/G]TTGGCCAGGCTGGTC | 9873 |
rs370364523 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093466 | GTATTAGGGATTCTC[A/G]AACTTACAGCTGGTG | 9873 |
rs370375451 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976416 | CCCACTTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 9873 |
rs370380429 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022579 | ATACTAATGAAAGAA[A/G]GAAAAGAATAAAAGA | 9873 |
rs370381174 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852237 | ACAGATGCTGGTGAC[A/G]TTATGGAAAAAAGGG | 9873 |
rs370382406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986683 | TTGCATGTAGATCTT[A/C]CAATATAAGGTTTTA | 9873 |
rs370402231 | in-del | -/GT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081783 | AAGGGCATCATAACT[-/GT]TGCTATTTCACAGGT | 9873 |
rs370413143 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857282 | TGTTACACTGTTTTC[C/T]TGACCCAGCATTTCT | 9873 |
rs370426539 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097017 | TTTTTTTTTTTTTTT[G/T]ATGAGACAGGGTCTC | 9873 |
rs370437908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987319 | TTTCATTTATCATTA[C/G]GCAAAATTAACCTCT | 9873 |
rs370473294 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967337 | TAGGCTGGTAACAGC[C/T]GAAAAGTGGAAACAA | 9873 |
rs370485215 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903928 | TATTGAGAGAGTTTA[C/T]CAGGTCCAACATGAA | 9873 |
rs370490694 | in-del | -/GTTTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892609 | GTTTTTGTTTGTTTT[-/GTTTT]TTGTTTTTTGAGACA | 9873 |
rs370494051 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874102 | CTCAAATAAAAAAAA[-/A]TTTAATGTGCCTAAG | 9873 |
rs370517191 | in-del | -/TATG/TATGTATG | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025992 | TATAGAGATTCATTT[-/TATG/TATGTATG]TATGTATGTATGTAT | 9873 |
rs370564816 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861215 | GTGATATCTCTACTA[A/G]TTTTCCAGATAATCA | 9873 |
rs370567817 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995082 | GAATCAAATAATATG[C/T]GGCCTTATGTTTCTC | 9873 |
rs370570752 | in-del | -/CAAAGAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084936 | CACCAGTGCAAAGAC[-/CAAAGAC]ATAAGAGTAAGAAGG | 9873 |
rs370571733 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959813 | GCTGATGAGCAGAGG[C/T]AGAACTATACTTCAA | 9873 |
rs370575074 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838271 | GGTTTCACTTTCTCA[A/G]TCTGGGGACTAACCT | 9873 |
rs370577358 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881132 | AATTATTCATGCAAC[A/T]AGGGACTAATATACG | 9873 |
rs370584105 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120899 | AGCACTGGATGTTAT[A/G]GGAACACACAGGCAG | 9873 |
rs370588594 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036378 | ACAATATTTCACAAC[A/G]TTATATCGGTCTTTG | 9873 |
rs370592445 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137922 | AGTGTTTGACCTTTA[C/T]CCAGAAGGCCACAGA | 9873 |
rs370594630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081305 | AGGGCATGGTGGCAC[A/G]CACCTGTAGTCCCAG | 9873 |
rs370601705 | in-del | -/TA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980675 | GTATGTGTGTGTGTG[-/TA]TATATATATATATAT | 9873 |
rs370604763 | in-del | -/TA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107036 | TTTTGTTAGAAAAGC[-/TA]TATATATATATATAT | 9873 |
rs370615702 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053329 | CTATTCATTGAGAGA[C/T]AATTTAAATTTAACT | 9873 |
rs370616838 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922890 | TTCCATTATCTAATT[C/T]CAGAACATTTCCACC | 9873 |
rs370633105 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080296 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 9873 |
rs370643448 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021882 | TCACTTGAGCCCAGG[A/C]AACACAAGGAGACCC | 9873 |
rs370661533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953672 | TAAATGTTATGGCAG[G/T]TTGTAATAAATACAA | 9873 |
rs370681950 | snp | A/C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999398 | GATCTCAGCTCACTG[A/C/T]AATCTCCACCTCCCG | 9873 |
rs370687106 | snp | C/T | 3.31175e-05 | 0.00406911 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984263 | AAACTGATATTGTAC[C/T]GCAAAACACATAGGA | 9873 |
rs370689006 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109152 | TGAAGTCAGGTAATG[A/T]GATTCCTCCAATTTT | 9873 |
rs370691571 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088779 | ATGAACTAGTTCACA[C/T]TTTCACCATTTAAAA | 9873 |
rs370700420 | in-del | -/CCTATTGT | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099090 | AGGTAGTGGTACATG[-/CCTATTGT]CCCAGCTACTCAGGA | 9873 |
rs370701482 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044911 | CCATCTCTACTAAAA[A/T]TACAAAAAATTAGCC | 9873 |
rs370751936 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026856 | ACTTCCCCCTTTGCT[C/T]GCTCTCTCTCCTGCG | 9873 |
rs370759240 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037636 | TTTCCTAAAAACTTA[A/G]GGCCCATACTGATTA | 9873 |
rs370799159 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867128 | CTGTAATAAATACCA[C/T]TGAGGAAATAAACAG | 9873 |
rs370817258 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078858 | AAGTAGTTACGACTA[A/G]AGGCATGCGTCACCT | 9873 |
rs370830651 | snp | A/G | | | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836574 | AGGATATTACACCTA[A/G]CACATGGGGGCTTCA | 9873 |
rs370859529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889268 | GCCCGGCTATAATTA[C/T]GTCTTTTAAAAAATA | 9873 |
rs370861205 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994371 | TTAGTCCTTGAAACG[A/G]CTCTATGAAAAAGGT | 9873 |
rs370871782 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954074 | CACTTTGGCTATTAC[A/G]CAGAGAATAGACATA | 9873 |
rs370899725 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873381 | TATGGGTCATTCATA[A/C]ATCTTCTTTGGAGAA | 9873 |
rs370908059 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112656 | TTGTTGGTGGTGGTG[G/T]TGGTGTTGTTGAGAC | 9873 |
rs370915712 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913825 | AACCAAAAAAAACCC[-/A]AAAAAAAAACAAAAA | 9873 |
rs370915900 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084187 | TGGACTTAACCAATG[G/T]AAGAGGGAACTAATG | 9873 |
rs370925163 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097508 | ACATTCCCTTTTCTT[C/T]TGTTTTTTTGGAATA | 9873 |
rs370929444 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841004 | TACTTGAGTTGTTGA[A/G]CAATAATGCTGATGC | 9873 |
rs370930426 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065180 | AAATCAGCTTCATAC[C/T]TGGGATGTAAGGCTG | 9873 |
rs370979720 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057015 | GTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 9873 |
rs370995018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110317 | GCAAAGCCATTAGGT[A/C]TTGGACTTGGCTTTG | 9873 |
rs371020243 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980343 | ATGAATCTGCTCCGT[C/T]GAAACTTTTCTTCAG | 9873 |
rs371024327 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070383 | GAACCTAGCATCACG[C/T]CAGTCGTAAAGTAGA | 9873 |
rs371074155 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917396 | CAAATCAATTGACCA[C/T]AGATGTTCAGGTTTA | 9873 |
rs371076366 | in-del | -/G | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140782 | CCACTTCAAACAGCG[-/G]AGAACAGCAAATGCC | 9873 |
rs371134360 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999315 | ATCTTACCAAAGATT[-/C]TTTTTTTTTTTTTTT | 9873 |
rs371136794 | in-del | -/GTTGTTGTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961426 | GTTGTTGTTGTTGTT[-/GTTGTTGTT]TTTAATAGATGGGGT | 9873 |
rs371168620 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977895 | ACTATTCAAAATAGC[A/G]AAGACTTGGAACCAA | 9873 |
rs371204300 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082802 | CCCCACATATAAAGT[A/C]ATTGCTTAAAGGGTC | 9873 |
rs371210131 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954822 | AGGCTACAAAGAATC[C/T]TGAAGTATTGAACCT | 9873 |
rs371222056 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945338 | TGCTGGGAATACTGG[C/T]TAGCCATATGTAGAA | 9873 |
rs371235112 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121843 | GAGTTCCTGATGCAG[A/G]AGATTAGGGATAAGC | 9873 |
rs371242867 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091472 | GAGAATCACTTGAAC[A/C]CGGGAGGCAGAGGTT | 9873 |
rs371254431 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058243 | AATCAGCCAGGCTGA[C/T]GCTACAGCAACCTGG | 9873 |
rs371260996 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024923 | CATTAGAAAAATGCA[A/T]ATCAAAATCACAATG | 9873 |
rs371262804 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914281 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT | 9873 |
rs371268181 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034672 | ACTACATCGCCTACA[C/T]TGTTGAAGTTTCCCA | 9873 |
rs371277740 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890015 | TACTGCTTTGTAGAT[A/G]GATCAGAAGGCCTTC | 9873 |
rs371282008 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004440 | CCTGATTCTACTCAA[A/T]CCCTTTAGAATTCTG | 9873 |
rs371294708 | snp | C/T | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72989048 | CCTTTAGCTAAATCT[C/T]TCACTGTCTCTTGTA | 9873 |
rs371306830 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038178 | GAGATCTGTCTCTAT[G/T]AAAAAATTTAAAAAT | 9873 |
rs371311109 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103661 | TGTAAAACCTACACA[A/T]AAAATACAGATATTA | 9873 |
rs371313184 | snp | A/T | 1.8592e-05 | 0.00304888 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001147 | CTCCTAAATTCAAAG[A/T]GGGATAGAAAAGCAT | 9873 |
rs371330272 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992047 | CTCCTTAAGCTGATA[A/G]GCAACTTCAGCAAAG | 9873 |
rs371332699 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950933 | CTAATTCAGTGTGAA[A/C]AGAAGTAACATTTGC | 9873 |
rs371339065 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120521 | GATCACCTGAGGTCA[C/G]GGGTTCGAGACCAGC | 9873 |
rs371381983 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918132 | TGGTTAAGTTTATTC[C/T]TAGATAGTTTATTCT | 9873 |
rs371394729 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025023 | CGTGGAGAAAAAGAA[C/T]GCTTATACACTGTTT | 9873 |
rs371403865 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937570 | TAGATGTTTCCATCT[C/T]CTGACCTCATGATCT | 9873 |
rs371405339 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988227 | CCTGAGTCTCAGCTC[A/T]CCTTCTCACAGATGT | 9873 |
rs371420183 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101901 | GAATATATTGTGTCT[-/A]TGTATGAAAACAGAT | 9873 |
rs371424307 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012161 | ACAAAAGTATAGTTC[A/G]TCAATACTATGGCAC | 9873 |
rs371437419 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068759 | AGGACTGCTTGAGCC[C/T]AGGAGTTCAAAACCA | 9873 |
rs371444969 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051671 | AGAGATGTACTGGCT[A/G]TGCAACAATAAAACC | 9873 |
rs371448419 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127699 | CATCAATTATTAAGG[C/G]GCAAATTATTCAGCT | 9873 |
rs371486749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123874 | ACTATAAATCAAAAC[A/T]AGGTGGTCAAACTGA | 9873 |
rs371551490 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965098 | CTGGCCAATCATTTT[A/C]CTTCTTAATTCAAAG | 9873 |
rs371566450 | snp | A/G | 5.52257e-05 | 0.0052545 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72902573 | AGGCTGGAACTGGAA[A/G]GGCTGGGGTTTGTGA | 9873 |
rs371582743 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058963 | TTCCACAGTCCTTAC[A/G]TTGATAGGCTAGCCT | 9873 |
rs371632308 | in-del | -/GG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114851 | TCTCAAGCGGAAGGA[-/GG]GGGGGTCTTTTTTGA | 9873 |
rs371645598 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863614 | TCTGATAAAGGATTT[C/G]TATTCAGAGTATAAA | 9873 |
rs371655675 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917802 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 9873 |
rs371674049 | snp | A/C/G | 4.94224e-05 | 0.00497083 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843269 | CAGGAGGCTGTTCGA[A/C/G]GTGGGAAACTGTAGG | 9873 |
rs371713208 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974158 | TAATTATAAACAACA[G/T]ACGTTTATTTGGTTC | 9873 |
rs371718185 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842789 | TCCCTCAGGAAAAGA[C/T]AACTCATCATCTGTC | 9873 |
rs371758125 | snp | A/T | 3.49583e-05 | 0.00418066 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000980 | ATAAGAACAGAAATA[A/T]AAACAATACCCTTTT | 9873 |
rs371765543 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129359 | ACAGGAGGTGAGTGG[C/T]GGGCAAGCAGGCCAA | 9873 |
rs371785507 | in-del | A/GAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940405 | AATATTAAAGGAAAT[A/GAT]ATATATGTAATGAGG | 9873 |
rs371791504 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060247 | AAACAAATGTCTAAT[C/T]GTACCATATTTTGGC | 9873 |
rs371799308 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001523 | TAATAAGGTAACTGA[A/C/G]GCCCAGAGAGATTTT | 9873 |
rs371819619 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110678 | ATTTATTTCTGCTCC[A/G]ATCTTTATTATTTCT | 9873 |
rs371820427 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912238 | AATCTTAGAGGAAAC[A/G]CATTCAGTTTTTCTC | 9873 |
rs371827007 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971820 | CTACAGAACTGTGAG[A/G]TAATAAATGGAGGTA | 9873 |
rs371845004 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980399 | TTATCCAGTTATGGG[C/G]GCTCATCAGAGTTAC | 9873 |
rs371869960 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860703 | TACAAAATTTAGCTG[A/G]GCGTGGTGGTGCTGG | 9873 |
rs371886568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943934 | TTTAATCATTATTCA[C/T]TGTGATGCTGCCAAC | 9873 |
rs371901947 | in-del | -/ATTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850385 | CAGAGATTTTTTTTT[-/ATTT]TATTTTTGAGACGGA | 9873 |
rs371922660 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068481 | GTAACAAACCTGCAC[A/G]TCTTGCATATATACT | 9873 |
rs371969922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026827 | CATGAGATCTAATGG[C/T]TTAAAAGTTTGGCAC | 9873 |
rs371995664 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971259 | AATGTTACAGTAACA[C/T]TGAGAAATATGAAAT | 9873 |
rs372015593 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905834 | TTCTTAATCCAGTCT[A/G]TCATTGATGGACATT | 9873 |
rs372047817 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862017 | ATATCTGAATAATCA[C/T]CAATGCAATTACACC | 9873 |
rs372054931 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944301 | CAACGACAAAAACCA[C/T]ATGATTATCTCAATA | 9873 |
rs372109238 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913833 | AAACCCAAAAAAAAA[-/C]ACAAAAAAAAAAACC | 9873 |
rs372120877 | snp | C/T | | | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72849773 | GTAGGAATAAACAAC[C/T]TTGCAGGTGAGTGGA | 9873 |
rs372155918 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997989 | TGAACTACCACTCCC[A/G]TCCCCAAAAGATGAG | 9873 |
rs372160233 | in-del | -/CCCAAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863659 | TAAAAATAAAACAAA[-/CCCAAT]AAAAATTAAACAAAG | 9873 |
rs372170666 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113521 | CTACAAGCATGTGCC[A/C]CCACGCCCAGCTAGT | 9873 |
rs372183073 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050106 | TTGGCTCTGCAGGCC[A/G]TAAGATCTCCAGGGC | 9873 |
rs372187815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083129 | TAAATCAACAAACTT[C/G]TAAAAAGTATTATTA | 9873 |
rs372206901 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103463 | TCAGAAATCATTACC[C/T]GAATCCCTAGGGTGA | 9873 |
rs372250808 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981679 | CTATGTAATACCTAA[C/T]ACGATACTAAAACCA | 9873 |
rs372258795 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838754 | AAACTCCAAGCCTGG[C/T]CTTGATTGTAGCAGT | 9873 |
rs372271675 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048323 | ATCTCCCTTAAGCCA[A/C]GGTTCATGATAGTCT | 9873 |
rs372280505 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003573 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG | 9873 |
rs372280601 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969862 | GGTTATGCTAGGTAC[A/T]ACACGACCAAATACA | 9873 |
rs372284799 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131307 | TGGATCACAAGGTCA[A/G]GAGATCGAGACCATC | 9873 |
rs372287081 | snp | A/G | 0.000149314 | 0.00863915 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887603 | TGGGACAATAATGAT[A/G]ACTGTTTTTTACTTT | 9873 |
rs372299821 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093977 | ATACTTTGGAAGGCC[A/G]AGTCAGGCGGACAAC | 9873 |
rs372301561 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121553 | TCTTGGGTTGCTAAG[A/C]TTTAAATGAAATAAT | 9873 |
rs372311035 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930684 | GGGAGGGAGGCTACA[-/A]GTAAGCCAAAATCGT | 9873 |
rs372311189 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910488 | GTAATAAGAAAAATT[A/C]TTCTGCCTTGGGATG | 9873 |
rs372311715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114612 | AGGTATTGCTGCTGG[C/T]TCCTCAGGGCCCAAG | 9873 |
rs372313536 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029257 | CTTACAAGACTATTG[C/T]AGGAGCAAATTCTGA | 9873 |
rs372332271 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840975 | CTAAGGGAGAAAACC[A/G]AAGAAGCTCATTTTA | 9873 |
rs372366696 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034027 | CCGATAGCAAATATA[A/T]CATCTTTTTTTAAGA | 9873 |
rs372391210 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963328 | AGTGAGCATTTACTA[C/T]GCACTATCTCATTTA | 9873 |
rs372401086 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878587 | CAAGGACTAACGGGG[A/G]TAATGTCAAAAGTAC | 9873 |
rs372425489 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862710 | TCCTGATAGGCTTTT[C/T]GGGGTAGAAAACCAA | 9873 |
rs372436241 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992327 | AATATCGTGAAAATG[A/G]CCATACTGCCCAAGG | 9873 |
rs372441212 | snp | A/G | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840359 | AATTGCAAAGTATCC[A/G]ACTGGATTACCGTGC | 9873 |
rs372465008 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039315 | TTGAGGTCAGGAGTT[A/G]GAGACCAGCCTAGAC | 9873 |
rs372481151 | snp | A/G | 3.39012e-05 | 0.00411697 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843143 | GAGTGCCTTGTTTCA[A/G]TCTTTACCACTGGCA | 9873 |
rs372521605 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895221 | CTGAGCCTTGGGACA[A/G]TTCTGGAAAACTCTG | 9873 |
rs372565576 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131274 | TGTAATCCCAGCACT[G/T]TGGGAGGCCGAGGCA | 9873 |
rs372572079 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101621 | TTTGTATTTTTTGTA[C/G]AGACAGGATCTTACT | 9873 |
rs372573511 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850427 | CTGTTGCCAGGCTTG[A/G]GTGTAGTGGCGTGAT | 9873 |
rs372581330 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069428 | AACTGAAAAAAAACT[G/T]GTATAAGAACATATA | 9873 |
rs372620540 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902378 | TGAGTTTCTTGGCCA[C/T]AATTCAGAAAAAAAA | 9873 |
rs372620576 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878933 | CCAACATGGTGAAAC[C/T]CCGTCTCTACTAAAA | 9873 |
rs372631550 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966719 | TCATGAAGTTTATAG[C/T]ACACTAAAGGTAGGA | 9873 |
rs372641793 | in-del | -/A | 0.24019 | 0.249807 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077097 | CTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 9873 |
rs372658067 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013739 | TTGCAATACTTTTTT[-/T]AAATTAGGGTTTATA | 9873 |
rs372669164 | in-del | -/AGA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935220 | CTTGTTTGAAGAAGA[-/AGA]TTATGATGAATTAGG | 9873 |
rs372678020 | in-del | -/AGTA | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980612 | CCACAGTCCTCCAGC[-/AGTA]AGTGATTTCCATCAC | 9873 |
rs372685355 | snp | A/G/T | 0.000165551 | 0.00909679 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841611 | GAAGCGAGGTTACCC[A/G/T]GTGCTCCCCTCCAGG | 9873 |
rs372687487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078999 | GTTGGGATTACAGGC[A/G]TGCGCTACCGCACCT | 9873 |
rs372687874 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102494 | GCAATGAAACGAAAC[A/G]TCCATCAACTGATGA | 9873 |
rs372694728 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035784 | GGAGTACAGTGGCGC[A/G]ATCTTGGCTCACTGC | 9873 |
rs372699005 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043968 | ATTCACCAATTTTGG[C/T]AACAAACTATTAGGT | 9873 |
rs372733176 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947725 | GTGATAAAATCATTA[G/T]TTAAAAAAAATATTG | 9873 |
rs372765515 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123341 | ATCCCTGAGGTCAGG[A/G]AAAGTATCTGAAATG | 9873 |
rs372779512 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097615 | TTCTTGTGAGGTGTT[-/C]TTTTTTTTTTTTTTT | 9873 |
rs372805734 | in-del | -/GTTC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873444 | TGAGTATTTTTGCCT[-/GTTC]TTTTATTATTATGAG | 9873 |
rs372808884 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937521 | CATGTCATGGACATA[C/T]GGGACCATTAATGGA | 9873 |
rs372841337 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843400 | ACAAAGACCAAAACA[A/G]ACTCCTAAAAATGTC | 9873 |
rs372850671 | snp | C/T | 0.000241687 | 0.0109902 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921806 | TTGGATAACACTACA[C/T]GTTGCACTAAAGGTA | 9873 |
rs372852511 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983074 | CTGAGGCGGGCGGAT[A/C]ACGAGGTCAGGAGAT | 9873 |
rs372858683 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097546 | TAGGATTGGTGTTAA[C/T]TCATCATTAACTGTT | 9873 |
rs372895283 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133855 | AGTCGCAAGATTCCA[C/T]TTCTATAGAGACAGA | 9873 |
rs372899478 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085530 | TTTCTCTTTTTCCCC[C/T]TTTGAGAGCCAGATC | 9873 |
rs372903933 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052223 | GATTTCTAAACTGTA[C/T]AAATCTATGAAAAAT | 9873 |
rs372905938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892073 | AAGAGAATGAATTTG[C/T]AGGGAGTAGCTAGAT | 9873 |
rs372923584 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953253 | GTAGTGAGGTAAACT[A/C]CAGATCTTAGATCTC | 9873 |
rs372925366 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967136 | ACCCGGGAGGCAGAG[C/T]TTGCAGTGAGCTGAG | 9873 |
rs372930452 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004630 | TACCCTTGCCTCTTT[C/T]TCTTTCCACCTTTAT | 9873 |
rs372934014 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017210 | GGCTCAACTCCTGGG[A/C]TCAAGCAAGCCACCT | 9873 |
rs372934826 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002723 | TTCTCCTAGTTAATA[A/G]CTGTTTGCCCTTCCA | 9873 |
rs372941463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984759 | ACGAAATAGATTTTG[C/T]AGAGCTTTCCAAAGC | 9873 |
rs372950360 | snp | C/T | 6.65059e-05 | 0.00576616 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849918 | GAAACCATTGGCTAG[C/T]TTCCTTACTTCAAGA | 9873 |
rs372956797 | snp | C/T | 4.25288e-05 | 0.00461114 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867983 | ACAGAAACACCAATC[C/T]GCTTTAGCAGGTCCA | 9873 |
rs372956857 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066885 | CTTACACTGTTGGTG[A/G]GAGTGTAAATTACTT | 9873 |
rs372961576 | in-del | -/ACACAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051869 | TAACACGGTATATAA[-/ACACAC]ACACACACACACACA | 9873 |
rs372970893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872063 | AAACATTACATAAAA[C/T]TTACTATCTGCACCA | 9873 |
rs372985899 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097059 | CCAAGCTGGAGTATA[A/G]TGGCACAATCTCAGC | 9873 |
rs372987116 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124689 | TGAACCAAGGGGGCG[A/G]AGGTTGCAGTGAGCT | 9873 |
rs372987922 | snp | A/T | 2.34277e-05 | 0.00342247 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72921879 | CTGCACAGCTTGGCA[A/T]GTTTCTAGCTCAGTC | 9873 |
rs372990461 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023248 | ACTACAAAGAGAATA[A/C]AAAGACAAGCTGCAG | 9873 |
rs372990609 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999590 | CATCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 9873 |
rs372996021 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918213 | TTCATTGATGGAATA[C/T]AGAGATGCAACTGAT | 9873 |
rs372996239 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009640 | AATTTACTTCTCCTT[C/T]ATTTATGAAGGATAA | 9873 |
rs373005159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068045 | AACCATCAGATCTCG[C/T]GAGACTTATTCACTA | 9873 |
rs373012061 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135071 | GTTGGCCAGGCTGGT[A/C/G]TCGAACTCCTGACCT | 9873 |
rs373024382 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987826 | TAAAAACGACTATGA[C/T]AGTATATTCCCAATG | 9873 |
rs373037782 | in-del | -/ACAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051868 | TAACACGGTATATAA[-/ACAC]ACACACACACACACA | 9873 |
rs373040966 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909186 | GGATTGCAGGCACAC[A/G]CCGCCACGCCTGACT | 9873 |
rs373042591 | snp | A/C | 0.000153988 | 0.00877327 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921963 | AGCCTGTAATAGAGG[A/C]GTAAATAAAAGAAAA | 9873 |
rs373046545 | snp | A/C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107286 | TCGATCTGACCTTGT[A/C/G]ATCTGCCCAGCTCGG | 9873 |
rs373047862 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954443 | ACTCCTGGGCTCAAG[C/T]GATCCTTCCCCTTCA | 9873 |
rs373054301 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886623 | TCCATACCCCTTCAC[C/T]ACATTGCTGCTGAGT | 9873 |
rs373075007 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865587 | CATTCCCTTCCTTCA[C/T]AACGAGAACAGCCCT | 9873 |
rs373087879 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948371 | CTTCAAAATTACTGA[A/C]TGTTTCATTTTTCAA | 9873 |
rs373101435 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003832 | AAAAGTATCAGCCAG[C/T]GTGGTGGCTCAAGCC | 9873 |
rs373133591 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846013 | ATGGGGTGTTTGATA[A/G]TATCTTCCTCATAGG | 9873 |
rs373137786 | snp | A/G | 0.00152016 | 0.0275276 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984246 | AATAAAATAATCAGT[A/G]CAAACTGATATTGTA | 9873 |
rs373143205 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851644 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATTGC | 9873 |
rs373171773 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945670 | CAAAGGGCTAATATC[C/T]AGAATCTACAATGAA | 9873 |
rs373184299 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052947 | CGCCTCCTAGGTTCA[A/G]GTGATTCTCCTGCCT | 9873 |
rs373197019 | snp | A/G | 3.29935e-05 | 0.00406149 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843543 | GAAGCCTGCAGTGTA[A/G]GATGGTCATGGACAA | 9873 |
rs373226801 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080044 | AGCTCATGCCTCTAA[A/T]CCCCAGTGCTTTGAG | 9873 |
rs373277761 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924474 | TTTTCAGTAGAGACG[A/G]GGTTTCACCGTGTTA | 9873 |
rs373288395 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914868 | GCAATTGCAACAAAA[A/G]CAAAAATTGACAAAT | 9873 |
rs373289650 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055300 | ATTAGCCATGATCAC[C/G]CCACTGGACTCCAGC | 9873 |
rs373295551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139109 | TAGTGCCTAAATATA[A/G]GAGAGGAAAAAAGGA | 9873 |
rs373334602 | snp | C/T | 2.18233e-05 | 0.00330321 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841433 | AAATGCATTTAGACC[C/T]ATGCCCAGGAGAACC | 9873 |
rs373338294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963900 | TTGGGGACCCTGGAT[G/T]AGATGACAACTCTGT | 9873 |
rs373377265 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873096 | GCACTTCGGGAGGCT[A/G]AGGCGGGCAGATCAC | 9873 |
rs373396483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106374 | TGGCACCACTACACT[C/T]CACCCTGGGTGACAG | 9873 |
rs373406058 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104702 | GCCTCCCAAGTAGCT[A/G]GGACCACAGGCACGT | 9873 |
rs373410364 | snp | G/T | 2.43028e-05 | 0.0034858 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72984090 | AAAGCTGTATTACCT[G/T]CATAATGTTAACTAA | 9873 |
rs373414387 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136440 | GGAGTCTCAGCTACC[A/C]TGGAGGATGAGATGG | 9873 |
rs373416543 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065706 | CATAAGCATTCCTAT[A/G]CATCAATAACAGACA | 9873 |
rs373424848 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087070 | TTGTATCATAGGAGA[C/T]GACAGCTCCATGCAT | 9873 |
rs373482789 | snp | C/T | | | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72844035 | CAAAAAAAGAGAGCA[C/T]TTCCTGGAAGTAGAG | 9873 |
rs373483930 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900829 | TTTCTATTAAACTGA[C/T]ACCATTAAACTCTGG | 9873 |
rs373494327 | snp | A/G | 2.06503e-05 | 0.00321321 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841511 | TATCTGGGCTGGGGT[A/G]GGGGCTGCTGGGAGG | 9873 |
rs373495264 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925786 | GGGTTGCACACTCCA[C/T]GGAGCCAGTGGCTAC | 9873 |
rs373510520 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866766 | TTCTCATTAGAAAAT[C/T]AGAATGCTATGTGAA | 9873 |
rs373522120 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050793 | CAGCAAATGAAAACT[A/G]TAATTAAGTTTTACC | 9873 |
rs373525177 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992839 | ATACCATTCAGGACA[C/T]AGGCATAGGCAAGGA | 9873 |
rs373530005 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974092 | GCGGGATGGAAGAAA[A/T]CAAAGTTTTGGTCCA | 9873 |
rs373531357 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907599 | AGATAATCACGTGGG[-/TT]TTTTTTTTTTTTTTT | 9873 |
rs373552324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913427 | GCATGTGCCACCACA[C/T]TTGGATAATTTTTGT | 9873 |
rs373554640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120819 | GCTCACAGTCTGGAG[A/G]TGAAGATATACCAAA | 9873 |
rs373565219 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992543 | CAAAACAGCATGGTA[C/G]TGGTACCAAAACAGA | 9873 |
rs373572752 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077114 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAAAAAG | 9873 |
rs373572906 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907567 | AAATTTTGTTGAAGG[A/C]CTTTTCTGCATCTAT | 9873 |
rs373579244 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879626 | TTTGAAATAAAAATT[C/T]ACAAGATGGCCTTAA | 9873 |
rs373583526 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045753 | AAGGGGAACATCACA[A/C]TCTGGGGACTGTTGT | 9873 |
rs373590228 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858594 | CACATAGAGGGGATC[A/G]ACAGACACTGGGGCC | 9873 |
rs373653514 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983273 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 9873 |
rs373665021 | multinucleotide-polymorphism | AA/TG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030366 | ATTATACTAAATAAA[AA/TG]AAACAAAAGGAGATA | 9873 |
rs373666755 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914765 | CTTAAATGTAAAACC[C/T]GAAACTATAAAAACC | 9873 |
rs373692654 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031368 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGTGG | 9873 |
rs373708559 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992691 | AAATGGTGCTGGGAA[A/T]ACTGGCTAGCCATAT | 9873 |
rs373719529 | in-del | -/TCTG | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034867 | AACCAAGACTGTCAA[-/TCTG]TCTGTCAACAACACA | 9873 |
rs373737720 | snp | A/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant, intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842634 | ACCTGAATCTCTCTC[A/G]TCCATGGAGTGTCAC | 9873 |
rs373756132 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118725 | CTATAATGATGATGG[C/T]AAACACTAACTGAGC | 9873 |
rs373764522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038674 | ACATAAACATGGGAA[C/T]AATAAACACTAGGGA | 9873 |
rs373805762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130106 | GTCTCAATCTCCTGA[C/T]CTCGTGATCCGCCCG | 9873 |
rs373842790 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083677 | TACCTAGAATGGGAC[C/T]TCCAATTTCAAGCTT | 9873 |
rs373855802 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840093 | ATGCTGCTCCAGCCT[C/T]CTAATCGCTCCCTAT | 9873 |
rs373901992 | snp | C/T | 0.000542959 | 0.0164677 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867892 | GCCATTACTGGTCAC[C/T]GCAGGAGGGCGGGCC | 9873 |
rs373902675 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915570 | GCTCATGCCTGTAAC[C/T]CCAGCACTTTGGCCA | 9873 |
rs373907491 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043087 | AGAACTTCTGCCACA[A/G]CGCTGAATAGGAGTG | 9873 |
rs373921854 | snp | C/T | 0.00058987 | 0.0171635 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838893 | AGCAGGAAACAATTA[C/T]GTAGTTTGTCAGTCA | 9873 |
rs373926714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128707 | ACTATCCAGCAATCA[C/T]GAGGAGAATCATTAC | 9873 |
rs373946798 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896643 | ACTTTTAGTGATCAA[G/T]CCAATAAGGGAGTTG | 9873 |
rs373949133 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121568 | ATTTAAATGAAATAA[C/T]AGATGTTTAACATTT | 9873 |
rs373949284 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067210 | GAAGCTGGAAACCAT[C/G]ATTCTCAGCAAACTA | 9873 |
rs373949897 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036576 | CCCTGATAAATTATA[A/G]TCATGATTACTGTGA | 9873 |
rs373952785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110339 | TTGGCTTTGCTAGGC[A/G]ATATTTTATTACGGC | 9873 |
rs373954970 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943077 | GCTCACTACAACCTC[C/T]GCCTCCCGGGTTCAA | 9873 |
rs373955787 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887911 | CATTAAGTTTGAGGT[A/G]GTTTGTTAAGCAACA | 9873 |
rs373969244 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930398 | CCCAAAATGCAATTC[C/T]TGTTTTCCAAATAAA | 9873 |
rs373976094 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011515 | TCTTGTGGTTTAGCC[C/G]TAGTGATGCTGGACC | 9873 |
rs374005398 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995937 | GTAGACTTAAGGGTA[A/G]TGTCCAAACCCAGTT | 9873 |
rs374006179 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894754 | GGTAAGTTTGGAGCC[A/T]AAACTCACTTGAGCC | 9873 |
rs374025849 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032003 | GAACTATTAACTAAA[C/T]TATGGTCATCAGTAT | 9873 |
rs374044633 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923233 | ATGCTGCAAAGTTAA[A/T]AAATAAATAAATAAT | 9873 |
rs374049137 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088888 | AAATTATGTATTTTT[G/T]ACCCTTTTAAGTTTA | 9873 |
rs374051157 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893250 | CAAGTGATCCACCTG[C/T]TCTTGGCCTCCCAAA | 9873 |
rs374051654 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128333 | AACTGGAAATGGGTC[C/T]CTGCAGCAAATCAGG | 9873 |
rs374054070 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852206 | GAATGGCTATTATTT[-/AA]AAAGTCAAAAAATAA | 9873 |
rs374054551 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070466 | TCTCGTTCTGTCGCC[C/T]AGGCTGGAGTGCAGT | 9873 |
rs374057481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950704 | TTTCCTTATTTCTTT[C/T]AGGATATTTTAATTT | 9873 |
rs374057500 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045051 | CTCCAGCCTGGGCGA[C/T]AGAGCAAGACTCCAT | 9873 |
rs374067751 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874948 | CTTTAAAGAGACAGA[A/G]CTTTTAAAAATAGTA | 9873 |
rs374080134 | in-del | -/TTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954197 | CAGTAGATGTGGGGA[-/TTT]TTTTTTTTTTTTTTT | 9873 |
rs374084325 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917608 | TTCGAAGACTGGGCC[A/G]AGTGCAGTGGCTGAC | 9873 |
rs374092549 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933638 | GTAAGGAAAAAAAGT[C/T]GATTCACATGGACAA | 9873 |
rs374093062 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890473 | ATCAACTTGCCACCA[A/C]ACCTCAAAAGCCAGC | 9873 |
rs374100201 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860850 | AATTAGAAAATATTT[C/T]GAACTGGATAAAAAT | 9873 |
rs374125531 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934491 | GCATACCACCATACC[C/T]GGGTAATTTTTGTAT | 9873 |
rs374142987 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911747 | TAGTTACATATGTTC[A/C/G]CTTTTGTTGCCTAGG | 9873 |
rs374145363 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959708 | CCCAATAGCTTTCTA[C/T]GTGTTTACTGAAAGG | 9873 |
rs374192684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853822 | TTTGCAAGTTATGTA[C/T]CTTAAAAGGGACTAA | 9873 |
rs374195299 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927853 | TAGATGGATCAGCAG[C/T]TGTTTTCAACGGGGA | 9873 |
rs374234294 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132486 | CTACCTTCAAAGCTC[-/TT]GTTTCCATTACCAGT | 9873 |
rs374276600 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865963 | GAGACCAAGTTTTGT[C/T]CATCTTCAGTTTGCC | 9873 |
rs374321817 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910810 | CCGAGAAACACCCAA[A/G]AATGATCAATAAATA | 9873 |
rs374321963 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031481 | GTCTCCGAAAAAAAA[-/A]GAGAGACAGAGAGAG | 9873 |
rs374334004 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999413 | CAATCTCCACCTCCC[A/G]GGTTCAAGCAATTCT | 9873 |
rs374368422 | in-del | -/CT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113214 | TTCTGAAGTCCTTCT[-/CT]GTGTTATCTCGAATT | 9873 |
rs374372834 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031110 | TGTTAAGTGAAATAA[A/G]CCAGATAGAAAGAAG | 9873 |
rs374388715 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840854 | ACTATGCATTCGATA[A/G]TCCTGCAAGATCAGA | 9873 |
rs374410891 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006006 | TCGAACCCCTGGACT[C/G]AAGTGGTCCTCCCGC | 9873 |
rs374415879 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859647 | TCCCCCACAGATAAG[C/G]GGGGACTGTAATGAA | 9873 |
rs374427786 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074375 | TGTGCAAGCATATGT[C/G]CAAGCATAAAATATG | 9873 |
rs374432808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005330 | ACCACTCTTCTGAAA[C/T]TGCTTGCCAAAGTCA | 9873 |
rs374486468 | in-del | -/A | 0.00952359 | 0.0683454 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897337 | AAAAAAAAAAAAAAA[-/A]GGATAGTTGTGTCTG | 9873 |
rs374494257 | in-del | -/CA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954892 | ACACACACACACACA[-/CA]GATATATACAGAAAC | 9873 |
rs374496379 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924456 | CTTTTTTTTTTTTTT[G/T]TATTTTCAGTAGAGA | 9873 |
rs374517176 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119932 | TTACAAAAGAAAGAA[G/T]TTTAATTGGACTTAC | 9873 |
rs374519488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106224 | ACCAGCCTGGGAACA[C/T]AGTGAGAACCCATCT | 9873 |
rs374522181 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862228 | GGCAAGGATTTCTGT[C/T]GACTCTCACCACTTC | 9873 |
rs374530016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094207 | CAGAGCAAGACTCTT[A/G]TCTCCCTGCACCAAA | 9873 |
rs374530499 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889436 | TCCAACATGAGTAGA[C/G/T]AGCTGACAGCACACT | 9873 |
rs374532248 | in-del | CTTTC/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912145 | GCTCTTTCTTTCTTT[CTTTC/T]GTCTGACTGCTGTAG | 9873 |
rs374537477 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062166 | TGATACCCAGGCAAA[C/T]AGGGTCAGGAGTGGA | 9873 |
rs374539465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093387 | CACAAAATTGCAAGT[C/T]GTGTCAGAAGTAAAG | 9873 |
rs374557443 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032794 | CTTCAAGAAACTTCA[C/T]ACAAGCTGGCATGGA | 9873 |
rs374563514 | snp | C/T | | | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72889829 | TTCTCTTACACTTAC[C/T]CGTTGTTGGTGAACA | 9873 |
rs374569447 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025545 | AACTAATGGGTACTA[G/T]GCTTAATACCTGGGT | 9873 |
rs374571969 | in-del | -/CT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896763 | ATTAGGGGGAAAATA[-/CT]AAAAAAAAAAAAAAA | 9873 |
rs374572551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998701 | GGAGGAAAAAATTGA[C/T]AATAAAAAATATTAG | 9873 |
rs374576330 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933133 | CCTGATCTCAGGGGT[A/G]AACTTGCAGGGTAGG | 9873 |
rs374587260 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949188 | GCGTGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 9873 |
rs374587409 | in-del | -/A | 0.0020032 | 0.0315846 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044832 | TCCCAGTACTTTGGG[-/A]GGCCGAGGCAGGTGG | 9873 |
rs374631580 | in-del | -/CTTTA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098411 | TGGGTAAAGAAAATA[-/CTTTA]TATGATTTTGATCTT | 9873 |
rs374643152 | in-del | -/AC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066875 | TAGGAACGCTCTTAC[-/AC]TGTTGGTGGGAGTGT | 9873 |
rs374653615 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992163 | AACTCCCATTCACAA[C/T]TGCTTCAAAGAGAAT | 9873 |
rs374657135 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907149 | TTGGCTCTCTATTAC[G/T]GCTGGAATGCCTGTG | 9873 |
rs374660835 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878941 | GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 9873 |
rs374661276 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083158 | TATTCATACTTGTAA[A/C]TACTTTACAAATATA | 9873 |
rs374663881 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918874 | TACCTTCAGAGTTAC[C/T]ATCCTAGAGAAAATA | 9873 |
rs374677204 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142396 | CACCACTCAGGCCGC[A/G]GGAATTTCCGGCCTC | 9873 |
rs374683303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058465 | TTTGAATACTACTAG[C/T]ATAACACATGATAGA | 9873 |
rs374688945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025024 | GTGGAGAAAAAGAAC[A/G]CTTATACACTGTTTA | 9873 |
rs374694171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937038 | CATTTAAATAGCAGA[C/T]TTCTGCTCATCAACC | 9873 |
rs374707465 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138499 | CCTGAACTGCTTCTG[-/A]AAATGTATTACTTTC | 9873 |
rs374737492 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876635 | CTTTAAAAGAACATA[C/T]ATTCTACTCATATGC | 9873 |
rs374744169 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916372 | TACAGTACAGTAGTA[A/G]CATGATCATAGCCTG | 9873 |
rs374746074 | snp | C/G | 1.69192e-05 | 0.00290849 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73015828 | AATCATTCCGATCAT[C/G]AGCTTTTACTCCAGG | 9873 |
rs374752473 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889227 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 9873 |
rs374777469 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861655 | AAAGGATAGGCCGGG[C/T]GCGCTGGCTCATGCC | 9873 |
rs374790939 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907627 | TTTTTTTTCTTGAGA[C/T]GGAGTCTGGCTTTGT | 9873 |
rs374815420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108610 | TCTGTCGCCCAGGCC[A/G]GACTGCGGACTGCAG | 9873 |
rs374821033 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112171 | CATTTCTTATAGGAC[A/C]GGTCTGGTGTTGATG | 9873 |
rs374821525 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027697 | ATTTCAGAGATGTTC[A/C/G]CTGCACTCCCCGCCA | 9873 |
rs374825143 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029045 | ATACAGCAATGAAAG[C/T]AGAAAGTTAGTCAAG | 9873 |
rs374829444 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043230 | GAGGTATGTTCTTTC[C/T]ATGCCCAGTCTGTTG | 9873 |
rs374865039 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903823 | GGATAATTGAGGAGA[C/T]GCAAAAAGTAGTAGG | 9873 |
rs374868216 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983065 | TTTGGGAGGCTGAGG[C/G]GGGCGGATCACGAGG | 9873 |
rs374876270 | snp | A/G | 2.01375e-05 | 0.00317307 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921810 | ATAACACTACACGTT[A/G]CACTAAAGGTAACTT | 9873 |
rs374881802 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881345 | AATCAGATATCATCT[C/T]ACCCCAGTTAGAATC | 9873 |
rs374900099 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846249 | GCAGTGGTGCCATCT[C/T]GGCTCACTGCAACCT | 9873 |
rs374906780 | in-del | -/AGAA | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954107 | GGTAGGGGTGGGAGT[-/AGAA]AGCCAATTAGAAGAA | 9873 |
rs374910065 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115594 | GAATAGGGAAGAGAG[A/T]AAACACGAGAGAGAA | 9873 |
rs374911982 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987376 | TTTTCACATTACTAC[A/T]GCAAGTAAGTTATTA | 9873 |
rs374946138 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854494 | TGGAGTGCAATGGTG[C/T]GATCATAGCTCATTG | 9873 |
rs374946704 | snp | C/T | 4.94262e-05 | 0.00497098 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843324 | TGGCCAACTTTATTT[C/T]GAGCCTGGGTAAAAG | 9873 |
rs375006222 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057823 | TTCCCCTCAGTTCTT[-/G]AGGGATCTAAGAGGA | 9873 |
rs375050705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043980 | TGGCAACAAACTATT[A/G]GGTGAGTGAGAAATA | 9873 |
rs375077629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971877 | TTTGTTACATAGCAA[C/T]GGAAATCAAATATAA | 9873 |
rs375091855 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132215 | ATAATTCATGAAACA[C/T]GATAACTTCCTTTTG | 9873 |
rs375101155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049290 | GGAAAAAATTAAAAC[A/G]TGACAGAAACTGTCT | 9873 |
rs375114793 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925588 | ATTCAAGAAGGAATT[G/T]GTTGCCACGGTGTAT | 9873 |
rs375183560 | snp | C/T | 3.42214e-05 | 0.00413637 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984067 | GAAGTAAAATTACCA[C/T]AGATATGAAAGCTGT | 9873 |
rs375211663 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103477 | CTGAATCCCTAGGGT[A/G]AACCAAATATCTGCC | 9873 |
rs375234198 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112022 | TCTACTTAAGAATAA[C/T]TTATACATCACAATT | 9873 |
rs375234960 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110151 | TCTGTAGTTTTCTTC[-/T]TTTTTTTTTTGATGT | 9873 |
rs375255208 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910153 | GCCCGGCTGCCCCAT[A/C]TGGGAAGTGAGGAGC | 9873 |
rs375264770 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066810 | GCCAGTTAGAATGGC[G/T]ATCATTAAAAAGTCA | 9873 |
rs375268428 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104848 | CAGGCCTGAGTCACC[A/G]TGCCTGGCCAACTTT | 9873 |
rs375284836 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107222 | ACCATACCCAGCTAA[G/T]TTTTGTATTTTTAGT | 9873 |
rs375294254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039299 | GAGGTGGGCGGATCA[C/T]TTGAGGTCAGGAGTT | 9873 |
rs375295493 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065007 | CCCTAACTCCTTTCA[C/T]GAGGCCAGCATCATC | 9873 |
rs375307992 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096656 | AAAAAGGTGCATCCT[C/T]GTGTTCTTCCTGAAC | 9873 |
rs375368255 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877212 | TTTTAATGATTAGTG[C/T]TTGTTCTCCTGTGAT | 9873 |
rs375373670 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893195 | TAGTAGAGATGGGGG[C/T]TTTGCTATGTTGGCC | 9873 |
rs375376049 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115371 | TGTATTTTTAGCAGA[A/G]ATGGGGTTTCACTGT | 9873 |
rs375393711 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972547 | CCCTTTTATCTGCTT[C/T]ATATATAAAGATTCC | 9873 |
rs375406196 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006432 | GCCCTGGAATCATCA[C/T]TGATTCCTCATTTGT | 9873 |
rs375411975 | snp | C/T | 9.77613e-05 | 0.00699079 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988934 | CATTTATTTGCATAA[C/T]AATTTTCTCAGAAAT | 9873 |
rs375435105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017817 | ACTTAAATTTCCTAA[C/T]GTAAACAATCACAAA | 9873 |
rs375464183 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934110 | AAGACACTGTCTCAG[-/A]AAAAAAAAAAAAAAA | 9873 |
rs375476948 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871179 | TGCTGCTTTGCTCCA[A/C]CAGCCATGCCTCTGA | 9873 |
rs375480927 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131092 | ATCACATCTAAAACA[C/T]CACTGAGGGCTGGGC | 9873 |
rs375482336 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845527 | TGCAGCACTAGTTGT[C/T]CAATGTAAGCAGACA | 9873 |
rs375488152 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015171 | ATTCTAAACAAACAT[A/G]TACTTTTAAGATATC | 9873 |
rs375490957 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945428 | GACTTAAATGTTAGA[C/T]CTAAAACCATAAAAA | 9873 |
rs375518533 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988316 | TTGTCACTGCAAAAA[C/T]CTCTATTATATTGCT | 9873 |
rs375537394 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122365 | TCTGCTGCAGCTGAA[C/T]GCACCCTGATAGCCC | 9873 |
rs375543755 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981681 | ATGTAATACCTAATA[C/T]GATACTAAAACCAGC | 9873 |
rs375550096 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084312 | CAATGTACAAGGCCA[C/G]TACAAATTGTGGTAT | 9873 |
rs375595227 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098676 | TAAACTGAGAAAGAA[A/C/T]AGTCTCTTCAACAAA | 9873 |
rs375601859 | in-del | -/GT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133816 | AAAAAAAAAAAAAAA[-/GT]AACCATTATGCCAAA | 9873 |
rs375617608 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978031 | ATGGATGAAGCTGGA[A/C]ACCACCATTCTGAGC | 9873 |
rs375628821 | in-del | -/ATATTTAT | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903207 | TATTTATTTATTTAT[-/ATATTTAT]TTATTTATTTATTTA | 9873 |
rs375656465 | in-del | -/TAA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890391 | AACAAAACAATATAA[-/TAA]CAGCAACACAATCTT | 9873 |
rs375668527 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040135 | TAATGTTACACAAAG[A/G]CTGAGTTCATTTGTT | 9873 |
rs375686070 | in-del | -/AGT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927487 | TGTATGTAGGGGAAG[-/AGT]GGAGTGTAAGGGAAA | 9873 |
rs375687642 | snp | C/T | 0.00018128 | 0.00951879 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72887473 | CTGCCACCTTACCTC[C/T]GCTTTACGAATATTT | 9873 |
rs375707210 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033287 | GCGAGATTCCGACTC[-/A]AAAAAAAAAAAAAAA | 9873 |
rs375709248 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890926 | AAATTACCCAAAGAG[A/G]CTTTTAATATAGAAA | 9873 |
rs375755254 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078285 | GGAAAACTGGCTGTA[C/T]CTACTAAAGTAGAAC | 9873 |
rs375788859 | in-del | -/GT/GTGT/GTGTGT | 0.496778 | 0.0400063 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959853 | TTTTAAGTTTCTAGG[-/GT/GTGT/GTGTGT]GTGTGTGTGTGTGTG | 9873 |
rs375791768 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124482 | AATAATGGGCCAGGC[A/G/T]CAGTGGCTCACACCT | 9873 |
rs375834190 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128964 | GCAACCTCCATCTCC[C/T]GGGTTCAAGCGATTC | 9873 |
rs375839124 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892140 | GTTACTGAGCAGCAT[C/T]TTAGGAATAGGTAAA | 9873 |
rs375843071 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102006 | CAGACCCAGATAAAA[C/T]CCAATGCTACAATTG | 9873 |
rs375875859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015104 | CTGCCTTGGCCTCCC[A/C]AAGTGCTGGGATTAC | 9873 |
rs375890603 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001598 | GATACAAGACGAAGA[C/T]TGGGTACCTGTATAT | 9873 |
rs375894869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045312 | GGAACACTTTTACAC[C/T]GTTGGTGGGACTGTA | 9873 |
rs375904291 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929030 | TTCCAGCTTCATCCA[C/T]GTCCCTACAAAGGAC | 9873 |
rs375942657 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956320 | AACCACCATTTGGCA[-/A]CCATCATAAAGGTGG | 9873 |
rs375954074 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870731 | CAGTGAAACCCTGTC[A/T]CTACTAAAAATACAA | 9873 |
rs375957423 | snp | C/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840448 | TGAGGAGAGGTAACT[C/T]TGCAATAATATATTC | 9873 |
rs375976990 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095751 | GAGGAAGCTTTCCTG[C/T]TCATAGTTTGAAGAA | 9873 |
rs375978223 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858051 | GTAAAATATTTAAAA[C/T]CCCTAACACATGTTT | 9873 |
rs375999717 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966104 | TATAACTACCAGCGT[A/G]ATGGATACATCTACA | 9873 |
rs376027855 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108978 | TTTCCAGCACCATTT[-/A]ATTGAAGAGACTGTC | 9873 |
rs376037263 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068961 | TCGAGGCTGCAGTGA[A/G]TCATGACTTCGCCAC | 9873 |
rs376047908 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931496 | TTCTGGCCAGGCATG[A/G]TGGCTCACGCCTGTA | 9873 |
rs376055737 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004434 | ACACCTCCTGATTCT[-/A]CTCAAACCCTTTAGA | 9873 |
rs376058381 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872725 | GTTGTTTCTATTTCT[C/T]GGCTATTATGAATAA | 9873 |
rs376069834 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061839 | TAAAACCCCCATCTC[C/G]CTGGGACAGAGCACT | 9873 |
rs376083184 | snp | A/G | 0.000163987 | 0.00905354 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868049 | ACCAAGAAAATGGTC[A/G]GAAATCAAGGCTTTT | 9873 |
rs376089245 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908178 | TAACATAATGACCTC[C/T]AGTTTTATCTATGTT | 9873 |
rs376098610 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969487 | CTTTGTCTTAATTTT[C/T]TGAGGGTAGAGAGTA | 9873 |
rs376103014 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935452 | AGACTTTGGTAAAAG[C/T]CAAGGATATAAATAT | 9873 |
rs376103099 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976994 | GCAGTGGCATGATCT[C/T]GGCACACTGTGACCT | 9873 |
rs376131197 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037341 | TGCTGTACAGTCTAT[C/G]TGTCTGGACAAACAT | 9873 |
rs376134705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058986 | GCTAGCCTCTATAAC[A/G]TAAGGTGAAATAGAC | 9873 |
rs376148389 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004441 | CTGATTCTACTCAAA[C/T]CCTTTAGAATTCTGA | 9873 |
rs376171133 | snp | C/T | 0.000407028 | 0.01426 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867816 | ACTACAGAGTCAAAG[C/T]ATGCTTCAGTGAAAA | 9873 |
rs376176748 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903256 | GAGTCTCGCTCTGTC[A/G]CCTGGGCTGGAGTAC | 9873 |
rs376183252 | in-del | -/GAAA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125798 | GAAAAAAGAAAGAAA[-/GAAA]ATGGAATACTAACAA | 9873 |
rs376186984 | snp | G/T | 0.00017584 | 0.00937491 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889802 | TGGCTTAAGGTGAAT[G/T]TAACTAGGACTTTCT | 9873 |
rs376190842 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014587 | AGCTTCATTGCCACA[C/T]TCTTAAGAAATCATC | 9873 |
rs376202576 | in-del | -/GA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885238 | AGTGGAAACCAAGTG[-/GA]AGATTATTTTATGCT | 9873 |
rs376204027 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135124 | CTCCCAAAGTGCTGG[G/T]ATCACAGGCATAAGC | 9873 |
rs376225949 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876627 | TATGTGTACTTTAAA[-/A]GAACATATATTCTAC | 9873 |
rs376230330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850168 | TCCCAGGTTCAAGAA[C/T]TCTCGTGCCTCAGTC | 9873 |
rs376244623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909526 | AGGAGCCCCTCTGCC[C/T]GGCCGCCCTGTCTGG | 9873 |
rs376254108 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941029 | GGGCTTGGAAAGGAC[C/T]GTATGTTCCACCATG | 9873 |
rs376264013 | snp | A/C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097112 | GGCTCAAGCAATCCT[A/C/T]CCACCTCAGCCTCCC | 9873 |
rs376268111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917818 | GCTTGAACCTGGGAG[A/G]TGGAGGTTGCAGTGA | 9873 |
rs376276570 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088501 | TACTAAAATAGTAAT[G/T]AAAGTTTTCTCTGGG | 9873 |
rs376277937 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943509 | ATGTGAACTTCATAT[C/T]ACCTTGGTTATTTAT | 9873 |
rs376279878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909880 | CCTCTGCCCGGCAGC[C/T]GCCCCATCTGGGAAG | 9873 |
rs376289743 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068858 | AAAAAATTAAAAAAA[A/C]AAAAAAATCAGCCAG | 9873 |
rs376293661 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124179 | AAAACCAAACACCGC[A/G]TGTTCTCACTCATGG | 9873 |
rs376310150 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925327 | TAGAAGTATATTACA[A/T]ATCAGGAATTATACA | 9873 |
rs376321678 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000136 | TTGGCAAACGGAAAA[C/T]TGGGGGGTTTTTGGT | 9873 |
rs376325787 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965806 | TAGAATCACACAGTA[C/T]GTCATCTCTTGTGAT | 9873 |
rs376326430 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932983 | AAGTTAAAGGAGTAA[C/T]TGATTTCATAAAACT | 9873 |
rs376337070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085757 | AGGGGAATCTGATTA[G/T]CAGAGTTACCACAAA | 9873 |
rs376355033 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017759 | TCTTCTAACCACTCC[C/T]ATTCCTACTTGCTAA | 9873 |
rs376370110 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051091 | GAGGCCAAGGTGGGA[C/G]GATCGCTTGAATCCA | 9873 |
rs376380363 | snp | G/T | 7.46714e-05 | 0.00610984 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838909 | GTAGTTTGTCAGTCA[G/T]TTCCTGACTCAGTAT | 9873 |
rs376386856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907747 | AGGCACCCGCCACCA[C/T]GCCTGGCTGCTAATT | 9873 |
rs376390504 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880226 | CGAATCCATGTGCAA[C/T]TGCTATCAAAATCAA | 9873 |
rs376390897 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966563 | CAAGCTCCCTGCAAA[C/G]AGACTGGTTTTTCAT | 9873 |
rs376396139 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003833 | AAAGTATCAGCCAGC[A/G]TGGTGGCTCAAGCCT | 9873 |
rs376398152 | in-del | -/AA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899735 | GTAAGACCCTATCTT[-/AA]AAAAAAAAAAAAAAA | 9873 |
rs376409633 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866836 | TCAGTTTCGCTAGCA[A/G]GCCTGCCTGATATCT | 9873 |
rs376421601 | in-del | -/AAAATAAAATAAAAT | 0.0225401 | 0.10374 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080961 | CTCAAAAAAACAACA[-/AAAATAAAATAAAAT]AAAATAAAATAAAGA | 9873 |
rs376431604 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071456 | CAGCACCTTGAGAGG[C/T]CGAGGCGGGCAGATC | 9873 |
rs376485432 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873347 | AAAAAAAAAAAATGA[A/C]TCTTTTCATGTGCTT | 9873 |
rs376486887 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872477 | TGCAGTCTTGACAAT[C/G]ACTATTCTACTTTCT | 9873 |
rs376508779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137370 | CACCAACAATCTCTG[C/T]CTTTACATATTATAT | 9873 |
rs376515630 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963945 | TCACAGTTGAATAAC[A/C]ATGGCTAATTAATAG | 9873 |
rs376521432 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106230 | CTGGGAACATAGTGA[C/G]AACCCATCTCTACAA | 9873 |
rs376604544 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018952 | TAAGTCAAGATCTCA[C/G]AATTCAAATAACTCA | 9873 |
rs376612008 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094843 | TAGCACTAAAATGAT[A/G]ACCTGAGAATACAAA | 9873 |
rs376635765 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120257 | ATCCTTGTATATTTA[C/T]TGAACTATGGAAGAT | 9873 |
rs376681390 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919953 | AGAAAAAAATAGATA[C/T]AAAACAAAAGCCCTA | 9873 |
rs376683085 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072010 | TATTTTTTGATCAGC[A/G]GTCAGGGCAGGGGAC | 9873 |
rs376721409 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850019 | CATAGAAATGACTAT[C/T]TTTCGCACTTACATT | 9873 |
rs376729911 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114359 | GGCCCAGGGCAGGTC[C/G]AGAAACGCTGTCCAA | 9873 |
rs376735962 | snp | C/T | 0.0010855 | 0.0232716 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841587 | GGAAGGAGAGATCTG[C/T]AGCAAAGGGAAGCGA | 9873 |
rs376751741 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085175 | TAAAGACTCATGCTT[A/C]TTCAAGAGTGCTTCA | 9873 |
rs376757976 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116542 | CTTCTTTCGTTTTTG[-/T]TTTTTTTTTCTTTGA | 9873 |
rs376758400 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124409 | GAACTTAAAGTATAA[C/T]AATAATAATTTTAAA | 9873 |
rs376772375 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855234 | GCTGAGATCGTGCCA[C/T]TGTACTCCAGCTTGC | 9873 |
rs376782235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126963 | GAATTGCTGGAACAC[A/G]GGAGGCAGAGGTTGC | 9873 |
rs376783595 | in-del | -/AG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057905 | TTTTTTTTGAGACAG[-/AG]TCTCGCTCTGTCGCC | 9873 |
rs376786680 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988720 | AATGTTCATTTACCT[C/T]CTTTTTCAAAATTCA | 9873 |
rs376799687 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127656 | TAAACAGCTTCAGAC[C/T]TGATACTCTCAAGAG | 9873 |
rs376799869 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040955 | TTTTTTAGCTCCCAC[A/G]TATCAGTGAGTGAGA | 9873 |
rs376801969 | in-del | -/CAA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920598 | TAACAACAACAACAA[-/CAA]AATTGTTCACTCAAA | 9873 |
rs376804937 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998858 | AAATTGGAGCCCTTG[G/T]GCACTGTTGGTGGGA | 9873 |
rs376826385 | snp | C/T | 2.25966e-05 | 0.00336122 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889779 | AGTTCCTTAAACTGT[C/T]TGACATTTGGCTTAA | 9873 |
rs376826474 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067478 | AACTTAAAGTATAAT[-/A]AAAAAAAAAAGAAAG | 9873 |
rs376843544 | snp | A/T | 0.000390016 | 0.0139591 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141846 | CCAAAGCCCCCCAGC[A/T]GCGCCCTTACCTTCC | 9873 |
rs376844755 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003529 | TCTTGCTCTGTCGCC[C/T]AGGCTGGAGTGCAGT | 9873 |
rs376854635 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992577 | ATAGACCAATGGAAC[A/C]GAACAGAGCCCTCAG | 9873 |
rs376873819 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881037 | CAGACAAATAGGACT[A/G]CATTAAATTAAAAAC | 9873 |
rs376886418 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958704 | TCAGAGAAAGGTCTC[C/T]TATCTCCTTCCCAAG | 9873 |
rs376887668 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120114 | CACCAAGAACAGCAC[A/G]GTGGAAACCACCCCC | 9873 |
rs376893943 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004019 | GGAGACTGAGGCAGG[A/C]GACTCGCTTGAACTG | 9873 |
rs376897053 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048587 | CTTTCATTCTGGGAC[A/C]CCATCTGAAGTAGTT | 9873 |
rs376900869 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080151 | AAAATAAAAATACTA[C/G]ACGGGTATGGTGGCA | 9873 |
rs376904269 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893371 | CCCAGGCTGGAGTGC[A/G]GTGGTGCAATCATGG | 9873 |
rs376912275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011048 | CAGCTGTGATTGTAG[G/T]GGCAGGGGTGGGTAG | 9873 |
rs376918746 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851720 | TGCACTCCGGCCTGG[C/T]GACAGAGCGAGACTC | 9873 |
rs376924376 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896014 | ACTTTTATAGACAAG[G/T]GAAATTTTTGCCAAA | 9873 |
rs376933062 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080333 | AAGAAAGAAAGAAAA[A/G]AAATTTTTCAAGGGT | 9873 |
rs376961182 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999641 | AACATTCTTTGCCCA[A/G]GAATGTCAGTTAAAT | 9873 |
rs376962688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904590 | GTTTATAAATATTTC[A/C]GTATGACATCTAAAA | 9873 |
rs376963310 | in-del | -/CTCT | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867380 | TAAAACTCACCTACA[-/CTCT]CTCTATGTGAGGAGA | 9873 |
rs376971494 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889364 | TCACAATTTTCTTTG[C/T]TAATTTTATGGTAAA | 9873 |
rs376981337 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963391 | CAGCCTCATATTACA[C/G]ATGAGCTAAGTGAGG | 9873 |
rs376985315 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086116 | ATACTTACATTATTT[A/T]ACAAGATGAGGCTGG | 9873 |
rs376985892 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842303 | TTAACCACAGAGCAA[C/T]GCCTTCCCTCTTCGG | 9873 |
rs377006140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931917 | GCCATTGTTTCATTG[C/T]TGTTGTTTTAAATTT | 9873 |
rs377012657 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034528 | CCAAGGAAATAGAGA[C/T]CAAAGTTTCCACTCT | 9873 |
rs377015764 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973232 | ATTAGCTGGGTGTGG[A/T]GGCATGTGCCTGTAA | 9873 |
rs377029329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002987 | TGGTTACAATAATAT[A/G]TGTTGAAGGAGTAAA | 9873 |
rs377049362 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097877 | CAGAGTCTTGCTATG[C/T]TATCCCAGTTGGGCT | 9873 |
rs377056635 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038456 | AAATGGGCAGTGACT[C/G]AAGATCACTCACCAC | 9873 |
rs377062818 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086740 | ATAGAAGTAAAAAGA[C/T]TGTACAGAGTATTAT | 9873 |
rs377080868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894362 | CCAGCCTGGGCAACA[C/T]AGCTAGACCCCAGCT | 9873 |
rs377101234 | in-del | -/GTTTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866271 | TTTTTGTTTTGTTTT[-/GTTTT]TTTTGTTTTTTGAGA | 9873 |
rs377109230 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870857 | GTGAGCCGAGATTGC[A/G]CCACTGCACTACAGC | 9873 |
rs377115275 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901249 | AAAATACAAAGAAAA[C/T]AGCCAGGCACAGTGG | 9873 |
rs377117989 | snp | A/C/T | 4.35713e-05 | 0.00466735 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841437 | GCATTTAGACCCATG[A/C/T]CCAGGAGAACCCTTA | 9873 |
rs377119952 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966847 | AGGAATATGATATAG[C/T]TTGAGGAAGGATTCC | 9873 |
rs377120511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965585 | ATTTCTGAAACTTTT[A/T]GTTAAAGTATAACAT | 9873 |
rs377121227 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933676 | CAAGTAATAATAATT[C/T]AATTGCTTTCCTTAC | 9873 |
rs377136825 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102840 | TTATAAATTATCCAG[C/T]CTCAGGTATTCTGTT | 9873 |
rs377145831 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997745 | TCCCTCTGTCATCCA[A/G]GCTGGAGTGCAGTGG | 9873 |
rs377168813 | in-del | -/TTAA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130700 | ACAAAAAAAGTTTAA[-/TTAA]ACAGACCCTCTCAAA | 9873 |
rs377175988 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976025 | TATGAAAAAGGAACA[A/T]GTGAGGAACAAATTA | 9873 |
rs377180154 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958868 | CATAAAAGGACATTC[C/T]AGTCTGCCAAAACAA | 9873 |
rs377182532 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998095 | AAAAAAGGGTGGAAA[A/C]CAAAATGCTGAAAAA | 9873 |
rs377184982 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909262 | GGCTGGTCTCCAGCT[C/T]TTGACCTCGAGTGAT | 9873 |
rs377212987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029321 | GTCTCCCAACCTAGA[C/T]AACAATCACACTGCG | 9873 |
rs377214009 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107629 | TCCAGTAAACTTCCT[C/T]CTACTCTCGAGTTCC | 9873 |
rs377216154 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077028 | GGCAGGAGAATGGCA[A/T]GAACCCGGGAGGCGG | 9873 |
rs377219319 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041337 | CTATACTAATTTACA[C/T]TCCTACCAACAATGT | 9873 |
rs377234825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848632 | ATTGGGCACTCTATA[C/T]GTTTATTCAATGATT | 9873 |
rs377235232 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992794 | ATGTTAGACCTAAAA[C/T]CATAAAAACCCTAGA | 9873 |
rs377235812 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905010 | ACGTTTACTTCCATC[A/C]GGAAGCTTGCTTCTT | 9873 |
rs377239317 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035108 | CTCAGGTTTAACTCC[C/T]GGACCTTGACAAGTT | 9873 |
rs377243961 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064001 | CACTCTTCTTAGCAC[C/T]ACATCACACTTATTC | 9873 |
rs377254910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922090 | AGATACAGATTGTAA[C/G]TAAATATGAACAGTT | 9873 |
rs377281883 | snp | C/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840105 | CCTCCTAATCGCTCC[C/T]TATATCCTTTCTGCC | 9873 |
rs377311663 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101785 | CAAAAATAAAAACAC[C/T]GATACCTATTCCAAC | 9873 |
rs377320397 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120713 | CAGCCTGGGCAACAA[C/T]AGCAAAATTGTGTCT | 9873 |
rs377330061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124712 | AGTGAGCTGAGATTA[C/T]GCCACTGCACTCCAG | 9873 |
rs377335309 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094317 | GAACTCTAACATGCC[A/G]TTGGTGGGAATGTAA | 9873 |
rs377337117 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062242 | AGGAAAACTAACAAA[C/T]AGAAAGGAATAGCAT | 9873 |
rs377341114 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029640 | AGGAAGTCATTGCAG[C/T]ACCCTTTCCCTATTG | 9873 |
rs377374757 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942521 | TGTATATGTAATACA[C/T]GCCTAGGAAAGATTA | 9873 |
rs377434750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088625 | TTTAAAAAAAATGCA[C/T]ATTCATAAACATGTA | 9873 |
rs377439592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993883 | TGCACGTTGTGCACA[C/T]GTACCCTAAAACTTA | 9873 |
rs377444126 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075553 | AACAGTTTGATCATT[C/T]GTTAAAAAGTTAAAC | 9873 |
rs377446138 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977809 | CGAGCAATCCCATTA[C/T]TGGGTATATACCCAA | 9873 |
rs377461624 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044783 | ATCATCTAACACTAA[A/G]GATGGGGCTGGGCAC | 9873 |
rs377472581 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992753 | ACCTTATACAAAAAT[C/T]AATTCAAGATGGATT | 9873 |
rs377475495 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909825 | GAGAAGTGAGGAGCA[A/C]CTCTGCCCGGCAGCC | 9873 |
rs377484374 | snp | C/T | 0.0036988 | 0.0428453 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984252 | ATAATCAGTGCAAAC[C/T]GATATTGTACTGCAA | 9873 |
rs377502346 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043061 | TCTTTCTCTTGACTG[A/T]TGCTCTGGCTAGAAC | 9873 |
rs377504447 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965235 | GTACATTATACTGTA[A/G]AAATATTGAACTACT | 9873 |
rs377509184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987297 | AACATCACTTCTTCT[A/G]TAAAGCTTTCATTTA | 9873 |
rs377510266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005375 | ATGGCTAGTCCAAAT[A/C]GTTCAAGTCTTGATT | 9873 |
rs377519029 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021803 | CGGATATATACAAAA[A/G]ACTGGCTGGGCGTGG | 9873 |
rs377532751 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902166 | AAGCGTGAGCCACAG[C/T]GCACGGCCTACTCTG | 9873 |
rs377534328 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915691 | GGCGCGGTGGTGGGC[A/G]CCTATAATCCCAGCT | 9873 |
rs377537934 | snp | A/C/G | 0.000149055 | 0.00863188 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72984146 | TGTGCATTTGCTGCC[A/C/G]CTAGGGTAAGAAGAT | 9873 |
rs377558770 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897316 | AATATTTTTTAAAAA[-/G]AGTAAAAAAAAAAAA | 9873 |
rs377561905 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118084 | CACTTTGGGAGGCCA[A/G]GGTGGGCAGATCACT | 9873 |
rs377583611 | in-del | -/A | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837465 | ATTTCTTAACCAAGG[-/A]AAAAAAAAAAAAAAC | 9873 |
rs377728144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986309 | CTGCCTCCTGGGTTC[A/G]TGCCATTCTCCTGCC | 9873 |
rs377728258 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948879 | ACCACGTTAGCTAGG[A/G]TGGTCTGGATCTCCT | 9873 |
rs377732924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023634 | TTTTGAAATTTCTTA[C/T]GAACAGAGACTTCCA | 9873 |
rs377733683 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068245 | AAAAATATGCCATTA[A/T]GTGCATGTTCTCGCT | 9873 |
rs377737266 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988209 | ATCAGTCAGCACACT[A/G]ACCCTGAGTCTCAGC | 9873 |
rs377759935 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859988 | GGACTGGACCCTTGG[C/G]GTACCATGAGGGAAG | 9873 |
rs377764706 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021138 | CACCTCTGCCTCCCA[A/G]AGGGCTGGGATTAAA | 9873 |
rs386374144 | in-del | -/AA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900676 | AAGCTGATTTGATTA[-/AA]AAAAAAAAAAGCACT | 9873 |
rs386374145 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907600 | GATAATCACGTGGGT[-/TT]TTTTTTTTTTTTTTT | 9873 |
rs386374146 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907618 | TTTTTTTTTTTTTTT[-/TT]TCTTGAGACGGAGTC | 9873 |
rs386374148 | in-del | -/AGGA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966207 | TCTGTCGCCCAGGAA[-/AGGA]GGAGTGCAGTGGTGC | 9873 |
rs386374149 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039250 | CTGCAGGGTGCAGTG[-/G]CTCACACCTGTAAGC | 9873 |
rs386754897 | multinucleotide-polymorphism | GTT/TTC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851217 | TTGAAAAAACAACCT[GTT/TTC]CACTGAAATTAAAAA | 9873 |
rs386754898 | in-del | G/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885242 | GGAAACCAAGTGAGA[G/TT]ATTTTATGCTAACAG | 9873 |
rs386754899 | in-del | CTC/GAGA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889462 | ACACTGCTGAGTGTT[CTC/GAGA]AAGTACAGAAAAAAC | 9873 |
rs386754900 | in-del | AT/TTA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928510 | CTTCCACTTAAATAC[AT/TTA]AATGATAATGATGGT | 9873 |
rs386754901 | multinucleotide-polymorphism | CTG/GTA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928677 | TTGAATCTTATTTAA[CTG/GTA]GGTGAGAGGAGGCCC | 9873 |
rs386754902 | multinucleotide-polymorphism | CT/TC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988385 | TCTTTTCCTACTTAT[CT/TC]TTAAAAAAAGGTCTT | 9873 |
rs386754903 | multinucleotide-polymorphism | AA/GC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023467 | TGTCATTACGGAAAT[AA/GC]AAACTAAAATAATGT | 9873 |
rs386754904 | in-del | AAAC/GTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042237 | GCTGAGATTATTTTT[AAAC/GTT]TCTGGTGAAAGACAG | 9873 |
rs386754905 | multinucleotide-polymorphism | CTG/TGT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062204 | CAAACTTCAGCAGAC[CTG/TGT]CAGCAGAGGGGCCTG | 9873 |
rs386754906 | multinucleotide-polymorphism | CGT/TGG | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140418 | CACAAGCTCAATCCA[CGT/TGG]CTAGGTCTTCCTACA | 9873 |
rs397727172 | in-del | -/GA | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885241 | GGAAACCAAGTGAGA[-/GA]TTATTTTATGCTAAC | 9873 |
rs397743939 | in-del | -/TCCT | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966210 | ATCGCACCACTGCAC[-/TCCT]TCCTTCCTGGGCGAC | 9873 |
rs397743943 | in-del | -/A | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861949 | AAAAAAAAAAAAAAA[-/A]GATAATATATCATTA | 9873 |
rs397747922 | in-del | -/CT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985695 | AAAGTCCTGGGACTC[-/CT]TGCCCTGTATGATGT | 9873 |
rs397748520 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132842 | AAAAAAAAAAAAAAA[-/A]CCTCAGGTGATTCTT | 9873 |
rs397748721 | in-del | -/CT | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985696 | AAGTCCTGGGACTCT[-/CT]GCCCTGTATGATGTA | 9873 |
rs397752452 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953638 | GGGGGAAAAAAAAAA[-/A]CACAAAAACTCTTGC | 9873 |
rs397757720 | in-del | -/AA | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900686 | GATTAAAAAAAAAAA[-/AA]GCACTACTATAAAGG | 9873 |
rs397766521 | in-del | -/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898746 | TTTTTTTTTTTTTTT[-/T]AAAGACAGGGTCTTG | 9873 |
rs397793205 | in-del | -/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962611 | CCCCCTTTTTTTTTT[-/T]AAACTAAGAATGTTC | 9873 |
rs397820243 | in-del | -/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892918 | GGTAATTTTTTTTTT[-/T]AAGACAGTGATATTA | 9873 |
rs397848524 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111476 | TCCTTTTTTTTTTTT[-/T]CAGTCTATGTGTGTC | 9873 |
rs397848553 | in-del | -/AC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121191 | CACACACACACACAC[-/AC]GCATGCACGCACACA | 9873 |
rs397849002 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108562 | TTAAGTTTTTTTTTT[-/T]GTTTGTTTTTTGTTT | 9873 |
rs397849055 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861410 | CAAAAAAAAAAAAAA[-/A]CTCCAGGACCAGATA | 9873 |
rs397849152 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046007 | TTTTTTTTTTTTTTT[-/T]AGAGACAGGGTCTCA | 9873 |
rs398016628 | in-del | -/AAA | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938198 | GCAAAACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 9873 |
rs398016629 | in-del | -/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956838 | GTCTTCTAGGGTTGG[-/T]TTTTTTTTTTTTTCC | 9873 |
rs398016630 | in-del | -/A | 0 | 0 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143611 | ACAGCCCCGTGACTC[-/A]AAAAAAAAAAAAAAA | 9873 |
rs398055242 | in-del | -/TTTTTTTTTTTTTTTTTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916985 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTT]GAAGCAGAGTGTTGC | 9873 |
rs398076031 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898745 | TTTTTTTTTTTTTTT[-/T]TAAAGACAGGGTCTT | 9873 |
rs398076032 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956837 | TGGAAAAAAAAAAAA[-/A]ACCAACCCTAGAAGA | 9873 |
rs398076033 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957031 | AGTCTTTTTTTTTTT[-/T]TCTTCTTTTTTTTTA | 9873 |
rs398076034 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116958 | TTTTTCCCCAAAAAA[-/A]ATCACTATTGTTATA | 9873 |
rs398115498 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039528 | CTCCAAAAAAAAAAA[-/A]GAAAGAAAGAAAAGA | 9873 |
rs527254458 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044823 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 9873 |
rs527281722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944661 | AAACCCCATTGTCTC[A/G]GCTCAAAATCTCCTT | 9873 |
rs527286541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845797 | CTTAGATTACTGTGG[A/G]TTTAAGTCCAGCTTC | 9873 |
rs527297703 | in-del | -/A | 0.000322619 | 0.0126967 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842848 | CAAAACATACTAGGG[-/A]GCAAGAGAAAAACAA | 9873 |
rs527300183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093307 | AATCATAACCTTACT[C/G]AGTAAACTTTCAGTG | 9873 |
rs527300920 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838217 | TGTGCGTTAATGCAA[C/T]TGGTGCTAAATTCAG | 9873 |
rs527306373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101251 | GTTGCACAGAAAATA[C/G]ATTGCATAAGAGCAA | 9873 |
rs527309727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945415 | AAGATGGGTTAAAGA[C/T]TTAAATGTTAGATCT | 9873 |
rs527319341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937538 | GGACCATTAATGGAA[A/C]GGCAAGGTCTGATCT | 9873 |
rs527322784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038089 | AAACAAAACCATCTA[C/T]CACTAAAAAATTCTT | 9873 |
rs527327047 | in-del | -/TAAA | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985179 | TCACAATAAAATTAC[-/TAAA]TATATTATTAAAATT | 9873 |
rs527337922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893316 | CCTAGATCATTCTTT[C/T]AACATTTTTCTTTTT | 9873 |
rs527349596 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992673 | AACGATTCCCTATTT[A/C]ATAAATGGTGCTGGG | 9873 |
rs527355810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884713 | AGGATCAAGCCTCTG[C/T]CTCCCAAGTAGCTGA | 9873 |
rs527386964 | in-del | -/TC | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968334 | ACTATAATTTATCAT[-/TC]TGTTTCCTAGAAAAT | 9873 |
rs527400247 | snp | G/T | 0.029116 | 0.117091 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938186 | AAGGAGTTTTTTTTT[G/T]TTTTTTTTTTTTTTG | 9873 |
rs527402881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930161 | AAAGCACTTAGGGCA[C/T]ATAATGTTGCTCCAT | 9873 |
rs527405468 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070423 | AATGTCAGGGTTTTT[C/T]ATTTTTATTTTTATT | 9873 |
rs527405487 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129465 | CAGCATTAGATTCTC[A/G]TGGCACGAACCCTAT | 9873 |
rs527415730 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074089 | CAGTGTGATATCGGG[-/A]AAAAAAATATTTCAA | 9873 |
rs527427328 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885511 | CTAAATGAAGACTCT[A/G]TGTGCCTGATACCTA | 9873 |
rs527428549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122517 | ACAGGAATGGCTACT[A/T]GTAAGAAATGGCCTG | 9873 |
rs527429814 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877509 | TTTTAATATTTTTAC[A/C]CCAGATTAATATTGT | 9873 |
rs527436715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086080 | AGAAAGCAGTGCTAC[A/G]GGGGAAATTTATAGC | 9873 |
rs527438146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930850 | CTAATGGGTACAAAA[A/C]AATAGAATAAGACCT | 9873 |
rs527441740 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123636 | GTCATCACACTATAA[A/T]GGCAATATTCAGGAA | 9873 |
rs527442516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941155 | CTCATAATTTAGGAC[A/G]GTCAAAAAAATAAAT | 9873 |
rs527459024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031549 | GTAATGCCAACATTT[G/T]TACTGGGTGTTACAC | 9873 |
rs527465850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878222 | AGTTCAAGGCTATAG[C/T]ACACTATGATTGTGC | 9873 |
rs527485065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086524 | GCAGAAAGAAGGAAA[C/T]ATTAATAATAAAGAT | 9873 |
rs527485142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077409 | TAAGAAGACTATATC[C/T]AGTGTTGAGGAAGAC | 9873 |
rs527557482 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871306 | TTGAAAATCTGCCAA[A/T]CCCTGACATTCAAGC | 9873 |
rs527563693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968139 | AGCATATAAGGCCTT[C/T]GGAATTATCTTGAGG | 9873 |
rs527569749 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974458 | TTAGGTTTCCAACAC[A/C]TGAACTTTAGAGGAC | 9873 |
rs527575711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914839 | GCAAAGATTTCATGA[C/T]GAAGATGCCAAAAGC | 9873 |
rs527583999 | in-del | -/ATG | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028659 | TGGGCCAGGGGTGGA[-/ATG]ATATGGTTTGGCTCT | 9873 |
rs527588334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870682 | GAGGGGGGCAGATCA[C/T]GAGGTCAGGAGATCG | 9873 |
rs527591234 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897214 | TAAATGCTTAGTATC[C/T]TATTTAATTTTCAAA | 9873 |
rs527595471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960413 | ATGCTCTAGTCTGCT[A/G]CTCCTTTGGATTTAA | 9873 |
rs527610222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070170 | GCCTTCATATAATGG[C/T]CTATTAATGACATGG | 9873 |
rs527622272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047627 | AAAACTGTTCCATGA[C/T]TTCTAACGGCAAATA | 9873 |
rs527631637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862171 | AACTTCATACTTAAT[A/G]GTGAAAGACTGAATG | 9873 |
rs527636874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017096 | CAAACAATCCTCCCA[A/G]CTCAGCCTCCCAAGT | 9873 |
rs527638917 | snp | C/G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969855 | ACACATTGGTTATGC[C/G/T]AGGTACAACACGACC | 9873 |
rs527639303 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929362 | CCCAGAATTCCCTGA[A/G]TTTTAATTACCACCT | 9873 |
rs527639565 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862886 | GGACAAACAGATCAA[C/T]AGAACAGAACAAAAT | 9873 |
rs527645855 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144009 | GGCCCTGACAGCTGC[A/G]GGGTGGCAGCTAGAG | 9873 |
rs527655535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908954 | CCATTGCATGTTGCC[C/T]TGTCTGCTATTTATA | 9873 |
rs527673570 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062216 | GACCTGCAGCAGAGG[A/G]GCCTGTCAGAAGGAA | 9873 |
rs527674163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136747 | TAAAAACCCAAGTTC[A/G]GGCCAGGCGCAGTGG | 9873 |
rs527684488 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961244 | AGTACTTTTTGTTTG[A/T]TTTTTGAGACAGAGT | 9873 |
rs527692452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909245 | TTTCGCCCTGTTGAC[C/T]GGGCTGGTCTCCAGC | 9873 |
rs527700181 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967181 | CTCCAGCCTGGGCGA[C/T]AGAGCAAGACTCTGT | 9873 |
rs527702324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854945 | GAGTTCGAGACCAGC[C/T]TGGCCAACATGGTGA | 9873 |
rs527702414 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135886 | TAAGGGGTGCGTTGC[-/A]GCAGTAGTGGCTCAT | 9873 |
rs527706491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008139 | AGGCCAGGAGTTTGC[A/G]ACCAGCCTGGCCAAC | 9873 |
rs527721273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953519 | TAAATCAATTTCAAC[C/G]ACATGAATTTATTGA | 9873 |
rs527729071 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144033 | GCTAGAGCCCAGGCC[A/G]TAGGTAGCGTAGGCT | 9873 |
rs527734343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054839 | GTGGGCCTGGTGGCA[C/T]GTGCCTGTAATCTCA | 9873 |
rs527735907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062701 | CCAGTGATTGAAGAT[A/C]AACTTAATGAAATAA | 9873 |
rs527746800 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965358 | TGAATTTTTACTGAG[C/T]GCTCTTCTATGCACT | 9873 |
rs527760608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010281 | CTCTTTGGTAAATTT[C/T]TCATTCATATCCTGA | 9873 |
rs527764167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001296 | ACATAACAAGCAACA[C/T]GGCATATACTCTATT | 9873 |
rs527768471 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003233 | TAGCACACTTCACTA[C/T]ACTTTCATTTCCTCA | 9873 |
rs527775949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102485 | AAACTGAAAGCAATG[A/T]AACGAAACATCCATC | 9873 |
rs527804106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946054 | TTACCGAGTATATAC[C/T]CAAAGGATTATAAAT | 9873 |
rs527810701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055336 | CAACAGAGTGAGACC[C/T]TGTCTCGAAAAAAAA | 9873 |
rs527817955 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894655 | AAGCATCTGGATCTC[C/T]GTATTCCAACTACAC | 9873 |
rs527822837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994091 | TCTCACTCCCTTGTC[C/T]TAGACCTGTCACTTG | 9873 |
rs527826739 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038103 | ATCACTAAAAAATTC[G/T]TATGACGAGGTGGGA | 9873 |
rs527839040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939375 | TCAAAAACCTTTCTA[A/G]GGAATGGTTTTTAAA | 9873 |
rs527842311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103279 | AGAAAAAATAAAACA[A/T]AATAAAAGTTGTAAA | 9873 |
rs527860429 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903646 | GGCATCTGATGGGGC[-/A]AAAAAACCCCACTTT | 9873 |
rs527863709 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107101 | CAGTGCAGTGGCGCA[A/G]TATCGGCTCACTGCA | 9873 |
rs527877908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839869 | CATTCGGCAAGAGTG[C/T]GTTCAACAACTTCAA | 9873 |
rs527879790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848313 | AATTTAACATTTCCT[A/G]AACACCCCACACTCT | 9873 |
rs527887207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113712 | AGGCATTTGAAGAAA[C/T]ACCCATTTGTACCCA | 9873 |
rs527889471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994568 | CCATGTTTTAAGATA[C/T]AGTGTAAACTCACGG | 9873 |
rs527897973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840550 | CAAATAGAGGCCTGG[A/G]AAATTAAATGCTTAC | 9873 |
rs527903420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886428 | CTTCTGTGTTACACC[C/T]GCAACAATCCCTCCC | 9873 |
rs527908992 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932756 | TTTTTGTTTAAGTTC[C/T]ATAAAGGGAGGCATC | 9873 |
rs527919105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040371 | AGTGTTTTCATTAAG[A/G]GCACTATTACAATAC | 9873 |
rs527937884 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962855 | CTGCCACAAAAGTTA[A/G]ATATCTTGATTTCAG | 9873 |
rs527947916 | snp | A/G | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144352 | AACCCCGTCTCTACT[A/G]AAAATACAAAAAATT | 9873 |
rs527948536 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986917 | TAATGTTCCTTGGGG[C/T]TCCAAACTCAACTTC | 9873 |
rs527959956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087757 | AGCCTAAGTGTATAG[C/T]GTAATAAATAAACAG | 9873 |
rs527976883 | in-del | -/TGTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932781 | GGCATCAGGTCTGTC[-/TGTT]TACCATTCCATCTTC | 9873 |
rs527996022 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932704 | CCTGATCATAGCATA[A/C/G]AACCTCATACTGGTG | 9873 |
rs528006420 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958384 | TTAGCTGGGCATGGT[A/G]GTGCTGACCTGTAGT | 9873 |
rs528013212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079755 | GGAGAACATTAAAGA[A/G]TAAGAAGAACTCAGA | 9873 |
rs528022687 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119906 | TAAAGACATACCTAA[C/G]ACTGGGCAATTTACA | 9873 |
rs528032944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866381 | TTCAAGCGATTCTTC[C/T]GTCTCAGTCTCCTGA | 9873 |
rs528033852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879761 | TGTGGAATGAGCTTT[A/G]CATATGACATGTAGG | 9873 |
rs528038861 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987693 | CTTCTCAGAAACGCC[A/C]CTCCACTGTGCTCAT | 9873 |
rs528044878 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101522 | ATGGCTCACTGCAGT[-/C]TCCATCTCCTGGGCT | 9873 |
rs528049254 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890111 | AGAAAGTTACCAGAA[A/G]AGTAAGATCAGCATA | 9873 |
rs528052095 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911258 | TTGTCCTTTCTCCAA[G/T]GTATGTTCTTGACAA | 9873 |
rs528056235 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861109 | AAAATCAATAAAATC[A/G]AAAGCTGATTCTTCA | 9873 |
rs528057618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134938 | CAACCTCCACCTCCC[A/G]GGTTCAAGTGATTCT | 9873 |
rs528078531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133346 | CATTATTAATAATAG[C/T]AAAAAGTAGAAACAA | 9873 |
rs528089606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013097 | CAACACCTCCATTAC[A/G]TTCTGAATAAAAAAG | 9873 |
rs528118235 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856894 | CTTAGAAGACATTGC[C/T]TTCATATTCTAGGAA | 9873 |
rs528121165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73141011 | TTAGGCAAATGTTTG[C/T]CCACGAGGGGAGGAC | 9873 |
rs528134078 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838103 | AAGATGTGGCTACTA[A/G]TTCAGCCCCTCCATA | 9873 |
rs528146605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096601 | TATACCACTTCCAGA[C/T]AGAATTATAGAATGT | 9873 |
rs528149022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058207 | TTAAAGGTATTGGAC[C/G]ATTATTGTTTTATGT | 9873 |
rs528152151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013870 | CTCCCATCTTAGCCT[C/T]CTAAAGCACTGGGAT | 9873 |
rs528161283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956656 | GAAAGGGCAAGAGGT[C/T]TCTCTGGGACTTCTT | 9873 |
rs528164962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004681 | GGTTAAATCTAAAAC[G/T]GTTTACATCACATCA | 9873 |
rs528171013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905791 | TTTTATGGCTGCATA[C/G]TATTCCATGGTGTAT | 9873 |
rs528194906 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963965 | CTAATTAATAGATGG[C/G]TAAACTTGGAAGTAG | 9873 |
rs528196435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949431 | CTCTAGCCTGGGCAC[C/G]AAAGAGCAAAACTCC | 9873 |
rs528199377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957511 | AAAAAAACTGAGGAA[C/T]TCTTCTAGATTGAAG | 9873 |
rs528207473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906439 | GTTTAATTAGATACT[A/G]TTTGTCTATTTTGGT | 9873 |
rs528223492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897987 | TTTAGAAATCAGTAA[C/T]TCTCTTATGGAAATA | 9873 |
rs528226975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850827 | GTGTGTGGTGGCTCA[C/T]GCCTGTAATCCAAGC | 9873 |
rs528268435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950438 | CTTGCATTTTTTTTT[C/T]CCCTCAAAGAGTTTT | 9873 |
rs528280028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942549 | TTAGAAGGATATGCC[A/C]AGATGACAGTAAGAG | 9873 |
rs528290418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851501 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGCG | 9873 |
rs528290577 | snp | A/G | 4.94393e-05 | 0.00497164 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843210 | GTGGAATTGCTGGAC[A/G]TGTGTGACCGACTGT | 9873 |
rs528302859 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72844137 | TCCTGCCATTTTCTG[A/G]AGGATGTGAGTCAAT | 9873 |
rs528303581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943241 | CATGTGATCTGCCCA[C/T]CTCTACCTCCCAAAG | 9873 |
rs528310257 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043221 | TATTTTGCTGAGGTA[G/T]GTTCTTTCTATGCCC | 9873 |
rs528313197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098856 | CCTTGGATTTTGCAA[C/T]GCATTCCTAGATGGG | 9873 |
rs528322645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071446 | CCTGTAATCCCAGCA[C/T]CTTGAGAGGTCGAGG | 9873 |
rs528335100 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859925 | AGAACAGCTGTCCCC[A/T]ATCTTTTAGGCACCA | 9873 |
rs528356293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990323 | ACCCTGGTAGGCAAA[C/T]TGCATCAATTTGGGA | 9873 |
rs528373245 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043986 | CAAACTATTAGGTGA[C/G]TGAGAAATAAATTTC | 9873 |
rs528385735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936030 | AAAACATCATGGGCA[A/G]CAGAAAACCTTGAAC | 9873 |
rs528410608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117135 | AGAAGCTGGTATTTA[C/T]AAGCTGGTACTTATA | 9873 |
rs528414941 | in-del | -/TTTC | 0.00244848 | 0.0349033 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897375 | CATGTACAGACTTTT[-/TTTC]TTTGTCTTATTTCCT | 9873 |
rs528417004 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092261 | GCCTCCCAAGTAGCT[G/T]GGACTATAGGTGTAC | 9873 |
rs528428539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928268 | ACAAAATTTTTTTCA[A/G]TGGCTCCCACTGTAT | 9873 |
rs528440829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882964 | ACTGGCATAAGTACA[G/T]ACATATAGACCAATG | 9873 |
rs528451507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029101 | GCACCATAAATATAA[C/T]GGTGTAGTACACTAA | 9873 |
rs528465730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124340 | GGTGCAGCACACTAA[C/T]ATGGCACATGTATAC | 9873 |
rs528468743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883471 | AAGACCAATCTAAAT[C/T]TGGGCAAAAGATATT | 9873 |
rs528532744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919590 | TCATGGGATTCAAGA[C/T]ATATCCCATGCTAAA | 9873 |
rs528538343 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075303 | AATTCCATTCCTTAG[A/G]TAAATACCCAATAGA | 9873 |
rs528541458 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849093 | TGGCGGAGGAGTGAA[C/T]CTGGTGCATGACAGG | 9873 |
rs528561336 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920718 | TACATTAAAATCAAA[A/C]AAATTATACAGTAAA | 9873 |
rs528576961 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981641 | TGTTCTTTGAAACTG[C/T]TGGTCCTTGTAAGTC | 9873 |
rs528586277 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043366 | GTATTTATCATCCTA[A/T]CCACTTTTCTGGGCA | 9873 |
rs528588470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131445 | GAGGCAGGAGAATGG[C/T]GTGAAACCAGAAGGC | 9873 |
rs528590123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022884 | GATCCCAGAAATAGA[A/C]CCATACAAATATAGT | 9873 |
rs528598150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076046 | ATCACCTGAGCCCCC[A/G]GGAGGTCGAGGCTGC | 9873 |
rs528604944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846418 | AACTCCTGACCTCGC[A/G]ATTCGCCCGCCTTGG | 9873 |
rs528610576 | snp | A/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139539 | TAACCTCAATAATAA[A/T]ATAAAATATGATAAA | 9873 |
rs528622406 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102440 | AAATGTGTACAAAAT[A/G]TGTACAGCAGCATTA | 9873 |
rs528629275 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047238 | TTGTTAAAACTACCA[-/T]TTTTTTTTTAATTAA | 9873 |
rs528646565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014953 | GGTTCAAGCAATCCT[C/T]CTGCCTCAGCCTCCT | 9873 |
rs528651503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913626 | TATTGTTCACAGTAG[C/G]CTCTAATGGTCCTTT | 9873 |
rs528663898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138757 | GGACTACAGGCGCAC[A/G]CCACCATGCCTGGTT | 9873 |
rs528680792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852279 | CTGCTGGTGGGAGTA[C/T]AAATTAGTTCAGCCA | 9873 |
rs528683330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060125 | ACCTCTGTGACTCTG[C/T]TACTGTATAAGGAGT | 9873 |
rs528705342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860943 | AGCACTTAATGCCAA[C/T]ATTCAAAAAGAAGAA | 9873 |
rs528708131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907432 | TCAAAGGGAATGCTT[C/G]CAGTTTTTGCCCATT | 9873 |
rs528725437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959391 | CCCGCCACCATGCCC[A/G]GCTATTTTTTTTTTT | 9873 |
rs528741358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061033 | GGCAAGATGGCCAAA[C/T]AGGAACAGCTCTGGT | 9873 |
rs528764503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951870 | TAGCGTTCAGTATAG[A/C]AGAGAAAGTCCTTAC | 9873 |
rs528777655 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990870 | GACCAGAACAGAACT[A/G]AACGAAATAGAGACA | 9873 |
rs528789724 | snp | C/T | 0.000128016 | 0.00799949 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900225 | AACCCACACTTCCCA[C/T]CCCTCCCGCCCTTGA | 9873 |
rs528793043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845071 | CCAGACGTTAATGTA[C/T]GTGACAGCAAACCAG | 9873 |
rs528805420 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061290 | GATACTGTGCTTGTC[A/G]CATGGTTTTCGCAAA | 9873 |
rs528809365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939956 | GTAGTAAAGTTCCAG[A/G]GAGTTTCTTCGAGAA | 9873 |
rs528814150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853143 | TCTTGCACTTAAAAG[C/T]TTTTTTAAAAATTGA | 9873 |
rs528826706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900696 | AAAAAAGCACTACTA[C/T]AAAGGGCAAAGGTTG | 9873 |
rs528828070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028599 | GGTGGACTGTTGAGA[C/T]GGCATGATTGTGTTT | 9873 |
rs528847471 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860143 | GCCTGCTGGTCTGAC[-/A]AGGACGCAGAGCTCA | 9873 |
rs528850475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040293 | AGAAGCTGTAATTGT[C/T]TCGCAGTCATGTGGA | 9873 |
rs528866332 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087721 | AAAAAAAAAAAAAAA[A/T]TTTTAAAATAAATTT | 9873 |
rs528868877 | in-del | -/TTG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101431 | GTACTCTTGTTGTTA[-/TTG]TTGTTGTTGTTGTTG | 9873 |
rs528876081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878936 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 9873 |
rs528878659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139858 | CCCCCACTGAAGGAA[A/G]AAGTTTGTATTGTGT | 9873 |
rs528905318 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908192 | CCAGTTTTATCTATG[C/T]TGTTGTAAATGACAG | 9873 |
rs528910007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856661 | CAGCTGAGTGAGGAA[A/G]TCCTGTGCTATCTCT | 9873 |
rs528911937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033171 | CGGGCACCTGTAGTT[C/G]CAGCTACTCGGGAGG | 9873 |
rs528922558 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894571 | TCTTTATGAAGTATA[A/T]TAATATATGGTTAAT | 9873 |
rs528927999 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138541 | ATTTCTTAGTTTGCT[C/T]AATAAGTTAAAAAAA | 9873 |
rs528963940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879635 | AAAATTCACAAGATG[A/G]CCTTAACAGTAGTTT | 9873 |
rs528968552 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136019 | TTTAAAATAAGCCAG[C/G]CATGGTGGCACGTGC | 9873 |
rs528969720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924484 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 9873 |
rs528987693 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928750 | ATTATACTTTAAGTT[G/T]TAGGGTACATGTGCA | 9873 |
rs528988481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871925 | CCCTCCGAATTCTCT[G/T]CTTGGGGAGTTGATA | 9873 |
rs528989747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025999 | GATTCATTTTATGTA[C/T]GTATGTATGTATGTA | 9873 |
rs528992350 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969799 | TGATAAAGAAGCAAA[A/T]TTCTTAGGCTTAAGT | 9873 |
rs529030676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970611 | AGCCACTGGTTTCTT[C/T]TGTGCATTACTTTCA | 9873 |
rs529042770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863679 | TAAAAATTAAACAAA[C/G]ATTTGAACAGACACT | 9873 |
rs529074152 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855886 | TGCTTTTTATATACA[A/G/T]CTATACTCTTTGAAC | 9873 |
rs529098976 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864238 | AGAACAGGGTGGGCA[C/T]AGTGGCTCATAAATA | 9873 |
rs529107078 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116990 | CTCTGTTTCATTTTT[A/G]GCATATTGATTTTTA | 9873 |
rs529116316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963151 | TGTTTTTAAAAAAAT[A/G]TTGTCTTTGTTTCAC | 9873 |
rs529117284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018944 | GGTTCAATTAAGTCA[A/G]GATCTCAGAATTCAA | 9873 |
rs529120593 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023785 | GTGAATGGATAAACA[A/C]ACTGTGGTACATAAT | 9873 |
rs529144875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954311 | ACACCTGGGCTCATG[A/C]AATTCTCTCAACTCA | 9873 |
rs529145343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111188 | ACTACCAGGTCCATT[C/T]GGTCTATAGTACAGA | 9873 |
rs529148049 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063721 | TTGGTAAAGTGATCA[A/G]TGCAGCAAGAAGAGC | 9873 |
rs529152265 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072999 | CAAGGAGCCGCCCTT[A/G]AAGTCCACAATGTTT | 9873 |
rs529164342 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010951 | TCTGGGTCTTGAGCA[C/G]TGTATGCTGGTGTTG | 9873 |
rs529164686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084725 | GTATTAACATTTATG[A/T]TACTGGAATGCATCT | 9873 |
rs529168014 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038624 | TACCACATGTTCTCA[C/T]ATCTAAGTGGGAGCT | 9873 |
rs529171919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116521 | GCATTATCAAAAGTC[A/G]TAATTCCTTCTTTCG | 9873 |
rs529200649 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910103 | GGAGCCCCTCTGCCC[A/G]GCCACCCATCGTCTG | 9873 |
rs529201226 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070325 | CTGATAACATTCCAG[A/C]ACTAAACAGCCTATA | 9873 |
rs529203529 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123667 | TTTGAATAAACTATA[C/T]GATCTTCTTAATTGC | 9873 |
rs529205894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104370 | CTCCCAGGTTCAAGC[A/G]CTTCTCTTGCCTCAG | 9873 |
rs529214660 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989417 | ACTGTTGGAGATATC[-/A]ATGATAATAAAATCA | 9873 |
rs529226200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002752 | CAGTCTCAGTTTAAA[C/T]GTAACTTCCTTTGGG | 9873 |
rs529244356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849203 | GCAAGAGAAGATTCA[C/T]GTATTCACGCCTCCC | 9873 |
rs529250453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995176 | ATTCCTTTTTATCGC[C/G]GAATAGTATTTTGTT | 9873 |
rs529255697 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032551 | ACTTAATTGCTCAGT[A/G]TTTTTAAAGCAAATG | 9873 |
rs529267866 | snp | G/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104853 | CTGAGTCACCGTGCC[G/T]GGCCAACTTTACTAA | 9873 |
rs529295576 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841287 | TATGAGCCGTGATCA[C/T]GCCACTGAACTCCAG | 9873 |
rs529296970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948377 | AATTACTGAATGTTT[A/C]ATTTTTCAACATTTT | 9873 |
rs529312933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041169 | ATAACTTGGCTACTA[G/T]GAATAGTGCTGCAAC | 9873 |
rs529313012 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042921 | ATCCTGCAATTCTAC[A/T]GAATTCATTTTTCAG | 9873 |
rs529322293 | in-del | -/TTC | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044747 | TGCAATAATTTAACA[-/TTC]TTCTAGCATGTTATA | 9873 |
rs529322977 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896983 | AGGTGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 9873 |
rs529331809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940891 | TACAAATTTTTTGAG[G/T]TTATCCTCATTGATC | 9873 |
rs529335034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987898 | GTTCACTGACTCTAT[A/G]AAAGTACAGGAAATA | 9873 |
rs529343015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842014 | GGGTCACAATCACCA[A/C]GCAAACAAGATCGGC | 9873 |
rs529372004 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988386 | CTTTTCCTACTTATT[C/T]TTAAAAAAAGGTCTT | 9873 |
rs529381459 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852163 | CAAATTGCTAAGATT[A/G]TAGGAGTGAGCCATC | 9873 |
rs529390176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880549 | ATATCCACCTGCCAA[A/G]GAATGAAACTAGATC | 9873 |
rs529412122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041922 | TAATCCACTTTGAGA[C/T]TATTATTATTTATTT | 9873 |
rs529420680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941466 | GCTTAGTATAAAATA[C/T]AGACTCCCAACTCTA | 9873 |
rs529422389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933494 | CTTAGCCAACAAATT[C/T]CTCTGTTTTGCCTAA | 9873 |
rs529427160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881417 | GATGCAGAAAAAAGG[C/G]AACTGTTATACACTG | 9873 |
rs529459283 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924779 | TAGATGACACCATTG[A/C]GCACTTCAAATTTAG | 9873 |
rs529475500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027746 | TAGGAAGGAAAAATG[A/G]TTTTGTAGCCCAGGA | 9873 |
rs529494488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035223 | ACTAAGACAAGGTCT[C/T]GCTCTGTCACCCAGG | 9873 |
rs529504221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980436 | ATTTCATTTGAAGAA[A/G]GGCAAAGATAAGAAT | 9873 |
rs529520714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081826 | AAACCAGATAACATA[C/T]ATAAAATACTCAGAG | 9873 |
rs529546956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874719 | ACATGGTATTTGCCA[A/G]CTCAGATTTAGACTG | 9873 |
rs529554223 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028245 | GTACCCTGCAGAGCC[A/T]CAAGGACAGAGATGC | 9873 |
rs529559659 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007519 | GCAGGAGGTGATGTG[A/G]AAGGATCACTTGGAT | 9873 |
rs529565771 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961560 | CATACCTGGCCTACT[A/G]TTGTTTTAAATGCGG | 9873 |
rs529568216 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032717 | CCCAAAGGAAATGAA[A/C]ATTGACATCTAAAAA | 9873 |
rs529597447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927353 | ACTGAGAATGTACAA[C/T]ACAAAGAATGAGCCC | 9873 |
rs529600275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972054 | TTGTACCTCAATAAA[A/G]TTGATTTAAAAAGAG | 9873 |
rs529601805 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107296 | CTTGTGATCTGCCCA[A/G]CTCGGCCTCCCAAAG | 9873 |
rs529620398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006452 | TCCTCATTTGTCTAT[A/C]ATATCTGCTCCATCA | 9873 |
rs529648284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951311 | AGTGGCAGAGTTGTA[A/C]GCAGTGATGAAACAG | 9873 |
rs529649812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073497 | GTAATACAAGTTTAC[C/T]TTGCATGTGCTTGAG | 9873 |
rs529655128 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950582 | CAATTTGTTGAAAGA[C/G]TATTCTTTCCTCCAC | 9873 |
rs529661388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108239 | GATCTTTTGCCCATT[C/T]CTTAATCAGATTATT | 9873 |
rs529670615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107650 | CTCGAGTTCCATGAG[C/T]TCAAATGTTTTCATT | 9873 |
rs529674731 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989652 | CCCCTGCCCAACTCC[A/G]TGGATACACATATAC | 9873 |
rs529674886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900165 | TATACATGTATATAC[A/G]TAACTTTCATCCCAA | 9873 |
rs529696717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051997 | CTGCAATAAAGAACC[A/C]ATTTCCAATGACACC | 9873 |
rs529698035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135410 | AATTTTTCCATATTA[C/T]AGACCTCCTTAAACT | 9873 |
rs529714697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099682 | CGTTAGGCTTAGCGG[C/T]GCTCACCACCCTGGT | 9873 |
rs529720916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951792 | AGGTTTACCCTTTCA[A/C]AATCTCTTTATAAAT | 9873 |
rs529725070 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837477 | AAGGAAAAAAAAAAA[A/C]AACAAACCACAACCG | 9873 |
rs529726555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991086 | ATACTATAAACACCT[C/T]TACGCAAATAAACTA | 9873 |
rs529736368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044241 | ATTATTGCCTCACTT[A/G]TTAACGCTGAATTCC | 9873 |
rs529757456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134846 | GGGAGTTTGTTTTTT[C/G]GTTTTTGGTTTTTTT | 9873 |
rs529758452 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052660 | AGTTTGGTCCTAATG[A/T]TTTAAAGGTGTGAAT | 9873 |
rs529768098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845658 | CTGTGGGCCTCTTGA[C/T]GCTTTGGCCCCTGCA | 9873 |
rs529775204 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73142901 | GACGACGCTCGCAGG[A/G]AAACGTTTGCAGTGG | 9873 |
rs529812643 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886138 | ACCTAAACCAGTGCA[A/G]GGATTCCTTGTATTG | 9873 |
rs529817944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037957 | AACTTATTTTATTTT[C/T]ATATGAAATATGTGA | 9873 |
rs529827925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936923 | TAAGTCCAATGTATG[A/G]ACTTCCTTGGAGACA | 9873 |
rs529829545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944578 | GAGAAGGAAATAAAG[A/G]GTATTTAATTAGGAA | 9873 |
rs529837591 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024184 | AAAATCTACCAGTGG[C/T]TGGGGGAACCGAAGA | 9873 |
rs529839579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892229 | TTATACCTTCTTATT[G/T]AGTATTCACTGTGCT | 9873 |
rs529865650 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937513 | TTAATAAACATGTCA[C/T]GGACATATGGGACCA | 9873 |
rs529881500 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898728 | ATTGCTTTTCTTTCT[-/A]TTTTTTTTTTTTTTT | 9873 |
rs529885578 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142154 | AGGAGGCGGAGACGG[C/T]GAGGGGGCGGGGGCC | 9873 |
rs529889493 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092784 | CAAGCATTTTGTGTA[C/T]ATCAAATCAAGGAGG | 9873 |
rs529898819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975798 | AAATTATCAACTAGT[A/C]AATGTATGTTTGGCT | 9873 |
rs529905272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877237 | TGTGATAAGCAACAG[C/G]TAAAATTTCTCCTGG | 9873 |
rs529910197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093694 | ACAACCTCCGCCTCC[C/T]GGGTTCAAGCGATTC | 9873 |
rs529920921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085285 | TAAGCAATGAGAGAG[G/T]ATTCTGGGAGATGGC | 9873 |
rs529921261 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138162 | TGTGCCACATCTCAT[A/G]TGTATTGTCATTTGA | 9873 |
rs529927877 | snp | C/G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915188 | TGCAAATCAAAACCA[C/G/T]CATGAGATACCATCT | 9873 |
rs529940416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878187 | TGGAGGCTGAGGCAG[A/G]AGGATCATTTGAGTC | 9873 |
rs529948606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865650 | ACTATCTCAAATGAC[A/G]TATCCTCCATGGGGC | 9873 |
rs529953102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984746 | GGTCTAAATCTAAAC[G/T]AAATAGATTTTGTAG | 9873 |
rs529957400 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847018 | ATTTATTTTTTAGAG[A/G]CAGGGTCTCACTCTG | 9873 |
rs529959601 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985897 | GACCAGTGATTTTTT[C/T]TTTAAAGCTGCAATG | 9873 |
rs529966875 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036324 | TAGGAAATAAAAGAC[-/A]AAAAAAAAAAAACCC | 9873 |
rs529972572 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128965 | CAACCTCCATCTCCC[A/G]GGTTCAAGCGATTCT | 9873 |
rs529979603 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112072 | TTTCTGTGTACTTAC[G/T]ATTACCAGTGAGTTT | 9873 |
rs529990484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076442 | AAGAAGACAGACAAG[A/G]AAGGAGACATACCAT | 9873 |
rs529991049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869404 | GAAAGGGAGGGGAGA[C/T]AGTGAAGAAGGGAAA | 9873 |
rs530008100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024359 | TATTTTAGCTAGAAA[C/G]TGTACGACTAAAGAC | 9873 |
rs530010230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914140 | CTGCCTCAGCCTCCC[A/G]AGCAGCTGGGACTAC | 9873 |
rs530045089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976630 | AGAAAACTGGAGGAA[C/T]CACATTACCTAACTT | 9873 |
rs530059669 | in-del | -/GGGGCGC | 0.0232847 | 0.105357 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73142874 | GTGTGTGTGTGTCGG[-/GGGGCGC]GGGGCGCGGGGGACG | 9873 |
rs530073736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016400 | TACAACCTTTTTTCA[C/T]TATTGTCCAGTCCTC | 9873 |
rs530074571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861437 | GATAACAGCCCTGGT[A/G]AATTCCACTAAACAT | 9873 |
rs530075772 | in-del | -/TAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872667 | TCTATTGTATGGATA[-/TAC]ATTAGAATGTTTATC | 9873 |
rs530080204 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875874 | CTTCTTGAAATATGC[G/T]GCCACCATGCTGGGG | 9873 |
rs530089767 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956316 | AGAAAACCACCATTT[A/G]GCAACCATCATAAAG | 9873 |
rs530090539 | in-del | -/T | 0.148661 | 0.22854 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959395 | CACCATGCCCGGCTA[-/T]TTTTTTTTTTTTTGT | 9873 |
rs530097851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061518 | GTGGTATGGGTCTGC[A/G]GGTCCCACCCCCACG | 9873 |
rs530130353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862036 | TGCAATTACACCATA[A/T]TAGCAGACTAAAAAA | 9873 |
rs530135705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008760 | AAAGATATAAAGATA[C/T]AGTTTGTGTCATTAT | 9873 |
rs530137764 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952637 | GCCTATAGTTAATTT[G/T]GGTAAGAAAATTTGG | 9873 |
rs530161988 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909200 | CGCCGCCACGCCTGA[A/C]TGGTTTTTGTATTTT | 9873 |
rs530185133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960172 | GTCATAGTGGAAGGC[A/G]AAGGCAGAGCAGGCA | 9873 |
rs530209355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017034 | AATGCCCAGGCTGGA[A/G]TGCAGTGGCGCGATC | 9873 |
rs530212518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108911 | GATTTGGTTTTTATA[C/T]ATGGCAAGAGACATG | 9873 |
rs530214819 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944719 | TCAGGATACAAAATC[A/G]ATGTGCAAAAATCAC | 9873 |
rs530215148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054733 | CAGGCTGAAGTGCAG[C/T]GGCACAATCATGGCT | 9873 |
rs530216552 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906733 | AAGATCAGATGGTTG[C/T]AGGTGTGTGGTGTTA | 9873 |
rs530219838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945506 | AAGGACTTCATGTCT[A/G]AAACACCAAAAGCAA | 9873 |
rs530222774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961038 | TGGGGAGGTAACACA[A/C]ATGTGAGGCTGCCTT | 9873 |
rs530224098 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927831 | GCACCAATAGGTACT[G/T]TTACTGTAGATGGAT | 9873 |
rs530234408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062154 | AGCCTCTGCTGATGA[C/T]ACCCAGGCAAACAGG | 9873 |
rs530273102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045877 | ACATATGTAACTAAC[C/T]TGCACAATGTGCACA | 9873 |
rs530278538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000485 | GTCCATTTGAAAACA[C/T]TTACTCATGTGTAAC | 9873 |
rs530297332 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088397 | ACAATGACGAAATTG[C/T]CTAACAATGCACTTC | 9873 |
rs530313484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133971 | AACATTTTAAATTGG[C/T]GTGACGATTGTACAA | 9873 |
rs530318057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854898 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGCAGGCA | 9873 |
rs530318094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846593 | TTAGGGACTACATTT[C/G]TTCTCACTTACCCCA | 9873 |
rs530323095 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054793 | TGATCCCCCCCACCT[C/T]GGCCTCTAGAGTAGC | 9873 |
rs530329603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847452 | GGGCTGAAGACACAC[A/G]GACAAGGTAAACATA | 9873 |
rs530341485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939303 | ATTCCCCCCTAAAAA[C/T]TGTAACTAAGCATTT | 9873 |
rs530342350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945989 | GGAAGTCAGTGTGGC[A/G]ATTCCTCAGGGATCT | 9873 |
rs530360358 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060893 | TAGCTTGAAACCAGG[C/T]ACTATAGTGAGATTC | 9873 |
rs530371545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087043 | CTTCAGGAGGTATAC[A/C]AGAAAAAGGCATTGT | 9873 |
rs530372220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894581 | GTATATTAATATATG[A/G]TTAATTATTTCAATA | 9873 |
rs530381501 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883854 | GGAGAATCGCTTGAG[A/C]CCAGGAGGTTCGGGC | 9873 |
rs530389554 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916817 | ATCTATGTTTTCTTT[A/C/T]GTTACTTGTGCTTTC | 9873 |
rs530390817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926725 | CAGGACAAGAACTTG[C/G]GCAAAGGCACCATGG | 9873 |
rs530393612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027708 | GTTCGCTGCACTCCC[C/T]GCCATCACAGGCCCA | 9873 |
rs530402079 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103157 | AATGTTCTATATATT[G/T]AGTGTAGTAGTGTTT | 9873 |
rs530404099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993946 | TCGGATAGAAAAGCC[A/C]GGCTTTGGGCTTCTG | 9873 |
rs530412936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873696 | TTTTTTGTAAGTTTA[C/T]TAGCTTTCGCTGTTA | 9873 |
rs530418260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126069 | TTCCACGGCCAGGTG[A/C]GGTGGCTCACACCTG | 9873 |
rs530425832 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917340 | ACCTTTTTCTGAAGA[G/T]AATATTCTTTCTCTA | 9873 |
rs530437541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140913 | TGGGGGTACATGTTC[G/T]AAAGAAAAGGACTCA | 9873 |
rs530445753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085998 | GGTTTTAAAGATGTT[C/G]AAAGAATTAAAGGGC | 9873 |
rs530468271 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095856 | AAAAGATAGTGAGAG[A/T]GCCTACACTATGAAC | 9873 |
rs530473700 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142069 | AGAGAGCGAGTGTGA[A/G]GAGACGAGGGAGGAG | 9873 |
rs530477130 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862633 | TTGGAAAACTGAATA[C/T]TGTTAACATGGCAAT | 9873 |
rs530478897 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930683 | TGGGAGGGAGGCTAC[-/A]AGTAAGCCAAAATCG | 9873 |
rs530479221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864617 | ATTAAAAAATAAATA[A/C]ATAAGAGTAAGGAAA | 9873 |
rs530496726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129472 | AGATTCTCATGGCAC[A/G]AACCCTATTGTGAAC | 9873 |
rs530498461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971440 | CAAAAGGGAGATTAT[C/T]TGCGATTACCTAATC | 9873 |
rs530520998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134718 | AAGTGTCTTTGACTT[C/T]GGTGAAACTCACGTT | 9873 |
rs530523085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072394 | TTCTTTAATGAAGTT[C/T]AAAAACTTAATTAAA | 9873 |
rs530531293 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070706 | GCTGGTATTACAGGC[A/G]TGAGCCACCATACCC | 9873 |
rs530544861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915681 | AAATTAGCCGGGCGC[A/G]GTGGTGGGCGCCTAT | 9873 |
rs530549362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065564 | AAGAGAGGAAGTCAA[A/G]TTGTCTCTGTTTGCA | 9873 |
rs530558686 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880869 | GATACCCTGTCTCGA[-/A]AAAAAAAAAAAAGAA | 9873 |
rs530565055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019901 | ATAAACCTATGTCTT[A/G]CAATTTTTTAAAGTT | 9873 |
rs530567340 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867768 | CTAGCAAACTATTAT[C/G]TTTTTAAAAAATTTT | 9873 |
rs530600536 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038509 | TACAGCGTGGATACT[A/G]TGCAGCCATGAAAAG | 9873 |
rs530609119 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948740 | GCACAATCTCGGCTC[A/C]CTGCAAGCTCCATCT | 9873 |
rs530612461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058149 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 9873 |
rs530631090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964915 | CTGCCTCAGCCTCCC[A/G]AGTAGCGGGGACTAC | 9873 |
rs530632717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955882 | ATATTACAGTGCATA[C/T]ATACATATATTTCCT | 9873 |
rs530633398 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850707 | TCAAATATGTAAGAA[A/T]TATTTATCAGTATCC | 9873 |
rs530655072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905316 | AGTAGGTATTTATAT[A/T]TATGGGGTACATAAG | 9873 |
rs530659981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857406 | ATACTAACGTTTACC[C/T]TTTCTTAGATGTTGT | 9873 |
rs530661826 | in-del | -/TAA | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923950 | TCTCAGAAAATAAAT[-/TAA]AAATAAATAAAGTTG | 9873 |
rs530667443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897917 | TTTCTAGAAAGAGCT[A/C]TGGCTTTCTGGTATC | 9873 |
rs530729838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850107 | TCGCTCTTGTCACCC[C/T]GGCTGGACTGCAATG | 9873 |
rs530741137 | snp | A/G | 3.3012e-05 | 0.00406262 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843180 | TTGAGGCTGCCTGAA[A/G]CGAGTTCTGCTTCCG | 9873 |
rs530746943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004492 | TATAAGAACCCACAA[C/T]CCATTTGGTCCTACC | 9873 |
rs530751770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118428 | ACCAGAGGAAACCAC[C/T]GTACTGACTTCTCCA | 9873 |
rs530752410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897187 | TCTGACTCAATGTGC[C/T]AGGCATTGAGTTAAA | 9873 |
rs530753029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980577 | TAAGCAATAAAAAAG[A/T]TAGCTATTATTATTA | 9873 |
rs530754918 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105749 | AATAAATTCAAATTA[C/T]ACTAATTATTTTTAA | 9873 |
rs530776593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943119 | TCCTTGGCCTCCTGA[A/G]TAGCTAGGATTACAG | 9873 |
rs530794585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043117 | GGTGAAAGTGGGCAT[A/C]CTTGTCTTACTCCAC | 9873 |
rs530818805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098341 | TGTTTAATTTCTACA[C/T]ATTTGCATATTTTCT | 9873 |
rs530825350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091563 | CAAAAAAAAGAAAAA[A/T]GAAAAGAAAGCAAAT | 9873 |
rs530828158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990248 | CTAGATCTGTGTTTC[A/G]ATAGAAACCTGATGA | 9873 |
rs530840345 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843054 | ATTATAGGACAGGAG[C/G]AAAGTTGTGCTTTTT | 9873 |
rs530853904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042420 | CCATTGTTCTATGTG[C/T]CTGTATTTATATCAA | 9873 |
rs530854343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036016 | GAGCCACCACTCCTC[A/G]CCCAGTTTTTATTAA | 9873 |
rs530861672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935922 | CTACTAGCATGCAAG[A/G]TAAGTCAGATGTCTG | 9873 |
rs530862263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982092 | TGTCTCTATATTTTC[C/T]AACCTGTATTCTAAT | 9873 |
rs530865223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889484 | TACAGAAAAAACACA[G/T]ATAATGCTTGAGCAA | 9873 |
rs530866888 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131594 | CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 9873 |
rs530873021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997794 | CAATCTCTACCTCCT[A/G]TGCTCAAGTGATCCT | 9873 |
rs530875272 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928908 | CCCCGATGTGTGATG[C/T]TCCCCTTCCTGTGTC | 9873 |
rs530875318 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996891 | TAAGTCTTAAATTCA[A/G]CTTAATGTTTTTCCT | 9873 |
rs530879197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117161 | TTATAACAAATACAT[C/T]CTACATGTACTAACA | 9873 |
rs530901674 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846291 | TTCAAGAAATTCTCC[-/T]TGCCTCAGCCTCCCA | 9873 |
rs530918101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035356 | TATTTTTTGTAGAGA[C/T]GGGGGTCTCATCATG | 9873 |
rs530920354 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064477 | CAAGAAAAACCCTTC[-/A]AAAAAAAAAATCAAT | 9873 |
rs530939542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124438 | AAAAAAGAAGAGAGA[A/G]AATGGGGCAGAAAAA | 9873 |
rs530947906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084308 | AAAACAATGTACAAG[A/G]CCACTACAAATTGTG | 9873 |
rs530949651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120612 | TGCATGCCTATAATC[C/T]CAGCTACTCAGGAGG | 9873 |
rs530952024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981318 | AAGACTTCAAAGTAA[A/G]TTCGAGAACATATAT | 9873 |
rs530955365 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973552 | CAGGGCATGATACTA[C/T]CTAAGACAACACTAT | 9873 |
rs530958424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880353 | AAGCTGGAGGTAATA[C/T]ACTACCTGACTTTAG | 9873 |
rs530984556 | in-del | -/TAAAATAAAATAAAA | 0.00322906 | 0.0401001 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080973 | CAAAAATAAAATAAA[-/TAAAATAAAATAAAA]ATAAAATAAAATAAA | 9873 |
rs530991529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882727 | GCCTAAATAAATAGA[A/G]AGACACATCATGTTC | 9873 |
rs531000753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875174 | ATGTATTACTATTTA[C/G]GACAGTGGTTTACTT | 9873 |
rs531008117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075237 | AATCACCTGAGAAAA[C/G]CATTTCATGATATTT | 9873 |
rs531019705 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911563 | TGCATTGAATCTGTA[A/G]ACTGCTTTGGGTAGT | 9873 |
rs531031385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859126 | AGTATAGCAGTCTCC[C/G]CTTATGTGTGGTTTG | 9873 |
rs531051039 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048270 | CCTCAGCTCATGCCA[C/G/T]GTACCGACACACATA | 9873 |
rs531060082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133018 | GCACATGAAAAAATG[C/T]TCACCATCATAAGTT | 9873 |
rs531069723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067032 | ATAAAGACACATGCA[C/T]ACGTATGTTTATTCC | 9873 |
rs531076341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966253 | CAACCTCTGCCTCCC[A/G]GGTTCATGCAATTCT | 9873 |
rs531095681 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029468 | GCTCAGCTGTGGCTA[A/C]CCATCTTTATCCCTG | 9873 |
rs531097502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021796 | CTAATAACGGATATA[C/T]ACAAAAAACTGGCTG | 9873 |
rs531112625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958622 | TTCAATATTTTCCTA[G/T]ACTGATCCATCAGTT | 9873 |
rs531128109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066542 | CAAAAGAAACTATCA[C/T]CAGAGTGAACAGGCA | 9873 |
rs531129217 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028467 | ACCCCCATTGTATCT[G/T]GGAAGTAACTAACTT | 9873 |
rs531131571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912996 | GGACACTTACAATCA[C/T]GGCAGAAGGCAAAGG | 9873 |
rs531136975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920643 | CATAGAAGGAACAAA[A/G]ATAAGATTTTTTCAT | 9873 |
rs531145710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851624 | GGCATGCGCCTGTAG[A/T]CCCAGCTACTTGGGA | 9873 |
rs531157990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868134 | CTGGATAAAGAAAAT[A/G]TGGTACATATACACC | 9873 |
rs531161448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022618 | GGATGGAGAGACATT[C/T]CATGTTAATGACTTG | 9873 |
rs531170510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014264 | AGCCTCCTGAGTAGC[C/T]GGGACTACATGCACG | 9873 |
rs531200165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957840 | AAGCACATAAATATA[C/T]AGTGAGGGAGAGGGA | 9873 |
rs531211425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114887 | TGTGCGCCCAAAACT[A/G]AGGGAGGGGTGGCAC | 9873 |
rs531216742 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024737 | AAATACTGCAAACTA[C/T]GCATCCCACAAAGGT | 9873 |
rs531218833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913477 | TTTCGCCATGTTGGC[C/G]AGGCTGATCGCGAAC | 9873 |
rs531221546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094735 | GTGCTTTTATTATCA[G/T]CAAATTGATAATTGT | 9873 |
rs531225841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906689 | AAACTGAATCCTTTC[C/T]CCATTTCTTGTTTTT | 9873 |
rs531250629 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103346 | ACTACTTCAGAACCC[A/G]CAAAACACTGAAATA | 9873 |
rs531254495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138872 | CTCAGCCTGCCAAAG[A/T]GCTGGGATTACAGGT | 9873 |
rs531255201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930894 | ACAATAGGGTGACTA[C/T]AGTCAATAATAATTG | 9873 |
rs531269701 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047971 | ATTATGTTAACAAAT[A/G]GTGGAGCCATAATTA | 9873 |
rs531275192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121529 | CCTATACAAATAATG[A/G]TATCTGCCTCTTGGG | 9873 |
rs531286618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055139 | AAACCATCAGATCTC[A/G]AAAGAACTCACTATC | 9873 |
rs531288624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102229 | TTAACAATTCCAAGT[A/G]CTGATAAGGATTTGG | 9873 |
rs531320337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118117 | AGGTCACGCATTCCC[A/G]AGACCAGCCTGGCCA | 9873 |
rs531321332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045783 | TGGGGTGGGGGGAGC[A/G]GGGAGGGATAGCATT | 9873 |
rs531337730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129802 | CAAAAAGGGTTGGGG[A/G]CCACTGCTGTAAACT | 9873 |
rs531344404 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087666 | GCCGAGATCACACCA[A/C]TGCACTCCAGCCTGG | 9873 |
rs531347471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078782 | GAAGCACAGTGGTGC[A/G]ATCACAGCTCACTGC | 9873 |
rs531350393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977680 | TCAGGAAACAACAGG[C/T]GCTGGAGAGGATGTG | 9873 |
rs531371695 | in-del | -/TATG | 0.23482 | 0.249539 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025996 | GAGATTCATTTTATG[-/TATG]TATGTATGTATGTAT | 9873 |
rs531376554 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068123 | CCACCAGGTCCCTCG[A/C]ACAACACATGGGAAT | 9873 |
rs531379271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025231 | TAGAAAAGACATGGA[A/G]TCAACCTAAACGCCC | 9873 |
rs531379983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031728 | GCCAGTCCACACTCC[C/T]GTTATTCTATTTCTC | 9873 |
rs531382728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939047 | ATACAGTAGCCAAAC[C/T]GTACTTTTTTGGGGG | 9873 |
rs531385725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969228 | AAACCTTATGAGAGA[C/T]GGAGCTGCATTCCAA | 9873 |
rs531393131 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986165 | TGGGTTTAAAAGATT[C/T]CTGTTATTTTTTACC | 9873 |
rs531411596 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070235 | AGTCTATTTCATAAG[G/T]CTATTTCTAACAAGC | 9873 |
rs531437758 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017123 | AAGTACCTGGGACTA[A/C]AGGCACATGCCACTG | 9873 |
rs531438698 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837377 | TGGCGAGCATTTCAA[A/G]TTTTTTAAGATTCTT | 9873 |
rs531445690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032518 | GGTGTGAGCCACCAT[G/T]CTTGGCCTATTTCTA | 9873 |
rs531461546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082065 | AAAATCGGCTGGGCG[C/T]GGTGGCTCATGCCTG | 9873 |
rs531473381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969677 | GTATGTTTTGACTAG[A/T]TAATTTAATAAGAAA | 9873 |
rs531478343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862996 | AGCACAATCATAGTT[C/T]GCTGTAACCTTGAAC | 9873 |
rs531478548 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961405 | ATTTTTAAGAAGTTT[G/T]TTGTTGTTGTTGTTG | 9873 |
rs531500657 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923977 | GTTGTCTTTTTGTTG[A/T]TGGGTTGTAAGAATC | 9873 |
rs531524554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129122 | TTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 9873 |
rs531527807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137207 | TCTTTGAAAAAAAAA[A/C]GCAAATCAGAAACCT | 9873 |
rs531537505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079389 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 9873 |
rs531538206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915679 | AAAAATTAGCCGGGC[A/G]CGGTGGTGGGCGCCT | 9873 |
rs531538252 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924408 | GCAGCCTCCCGAGTA[A/G]CTGGGACTACAGGTG | 9873 |
rs531538936 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020457 | TACTATACCATTTTG[G/T]CATGAAATTCCCGGC | 9873 |
rs531539126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863560 | TAAGGAAATAAAAAA[A/C]TAAGCCACAGACTAG | 9873 |
rs531539287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855013 | GCACGGTGGCTCACA[C/T]CTGTAATCCCTGCAC | 9873 |
rs531550134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855733 | GAGTGTAAAAAATGA[C/G]TTAGATCCACAGGCA | 9873 |
rs531567343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110380 | TTATTTGTTATTGCT[C/G]TGTTCAGGTTTTGGA | 9873 |
rs531599373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923075 | CCTGGCTTCTGTTGC[A/C]CAGCATAATATTTTC | 9873 |
rs531603698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062251 | AACAAACAGAAAGGA[A/G]TAGCATGTGCACTCA | 9873 |
rs531610909 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982229 | CCTTCAACACTCTTG[-/T]TTTTGCCTGAAGGTC | 9873 |
rs531617918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002174 | GACAGTGTAGAAGCA[A/G]GAAAAAGAAAAATTG | 9873 |
rs531618304 | snp | A/G | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841760 | AAGCTCCAATTTTGC[A/G]TTGCACTTCACTTTT | 9873 |
rs531629959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010843 | TGGCTTACTCAGATG[C/T]TGGTAGTGGCAGCAG | 9873 |
rs531630236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103426 | TAAGATTTAATTAGA[C/T]TTAGTTTAGGTATCC | 9873 |
rs531644993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895575 | AGCACATAACTAATG[C/T]GTCTATGCAAAGATC | 9873 |
rs531646161 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954921 | ACAGATCTGGCTGTA[C/T]GTATATGTAATAAAG | 9873 |
rs531663490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909724 | CGCCTCTGCCTGGCC[A/G]CCACCCCGTCTGGTA | 9873 |
rs531667401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062868 | GAAAACACACTTCAG[C/T]GTATTATCCAGGAGA | 9873 |
rs531667620 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904070 | ATACACCACGGAGTG[C/T]GTAAAGGGTACGAGA | 9873 |
rs531692671 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130626 | ACCAAGAGTCACCAA[C/T]AGGAAGAGGTATTAC | 9873 |
rs531715447 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143131 | GCACTCTACTGCAGG[A/G]CATTCAAGTCAAACA | 9873 |
rs531727802 | snp | A/C/G | 0.00677183 | 0.0578675 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063695 | AAAGAGACAAAGAAC[A/C/G]GTATTACATATTGGT | 9873 |
rs531728829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887416 | AGATGTATATCACAG[C/T]TGTGACAGTGTCATT | 9873 |
rs531729233 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954267 | CTGGAGTGCAGTGGC[A/G]CAGCATGGCGGCTCA | 9873 |
rs531738325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848932 | ATCAAAACGATTTAC[A/T]TTGGAAAAAAATGCT | 9873 |
rs531745747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848341 | TCTCATCACACTCTG[A/T]CTCTATACCTGCTGT | 9873 |
rs531749373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903472 | GATCCACCGGCCTCG[A/G]CCTCCTAAAGTGCTG | 9873 |
rs531749650 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973109 | CGCGGTGGCTCATGC[C/T]TATAATCCCAGCACC | 9873 |
rs531766735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888205 | AAAAATCTAGGTATG[A/G]CCAGAAAGGCAGAAG | 9873 |
rs531774543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946836 | GTTAAGTATAATGCC[C/T]AGGGAAATTTTTCAA | 9873 |
rs531778294 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975655 | TTATTATGTATCAAT[A/T]TTAGAAAGGATTTGT | 9873 |
rs531799864 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078164 | TATATACTCACCAAA[A/C]TGTCAGTCTTTTTAA | 9873 |
rs531815455 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003807 | ATATGAAGCAATTGT[C/G]AAGGATAAGAAAAGT | 9873 |
rs531823151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097086 | CAGCTCACTGCAGCC[G/T]CGACCTCCCAGGCTC | 9873 |
rs531827881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096105 | CGAGGTATCTAAACA[C/G]ACGTAAAATTTTTAA | 9873 |
rs531853027 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047646 | TAACGGCAAATATTT[A/T]TGCTCTTTCTTTCAG | 9873 |
rs531854590 | in-del | -/AAACAAAC | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868691 | GCAAGACTCTGTTAA[-/AAACAAAC]AAACAAACAAACAAA | 9873 |
rs531857195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041836 | AAATTTTTGCCTAGG[C/T]CAATGTCCTGGAGTA | 9873 |
rs531859118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840601 | TAGCCCGCTTTAATG[C/T]TCATAAAGTTTGTTC | 9873 |
rs531866943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988376 | CCAGTTCCTTCTTTT[C/T]CTACTTATTCTTAAA | 9873 |
rs531872755 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904028 | TAATCTGGGAACTGG[A/G]CGAACCAAACAGACT | 9873 |
rs531873030 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015694 | AATTATATCCGAAAA[C/T]ACAGCAGAGGAAAGA | 9873 |
rs531875192 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127547 | AGATCACCCCTGAAG[A/G]CTGATACCAACAACA | 9873 |
rs531877770 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995102 | TTATGTTTCTCACTT[C/G]TTTCACTTATCAAAA | 9873 |
rs531880028 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008757 | TACAAAGATATAAAG[-/A]TATAGTTTGTGTCAT | 9873 |
rs531881463 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096559 | AAGGAAAGGAAAGGA[A/C]AGGACAGGACAGGAT | 9873 |
rs531881973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112845 | CTTATTTAGTATTTT[C/T]AGTAGAGATGGGGTT | 9873 |
rs531882740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080756 | CAAAACCAGCCTGGA[C/T]AACATTGTGAAACCC | 9873 |
rs531886856 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110806 | GATGTAGGTACTTAT[A/C]GCTATGAACTTCCCA | 9873 |
rs531890579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034724 | CTTATTTGCACAAAA[C/T]GACCTGCAAATTTTA | 9873 |
rs531890724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027226 | ACCATTGATCACTGA[C/T]AGTGATATGGGCAAT | 9873 |
rs531900607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940702 | ATTCATGTTCACCGT[G/T]GTGGCAGAAAACGCC | 9873 |
rs531913648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881203 | ATGTAATCTTATTAA[A/G]AATTGGGCAATGGAT | 9873 |
rs531918603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041068 | CAGAATTTCATTCTT[C/T]TTTATGGCTAAATAG | 9873 |
rs531920668 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114929 | CGGACGCCATGGCTG[C/G]TGTCTCACTAGGTCA | 9873 |
rs531944254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119753 | TACCTGGCCTAGACA[A/G]CCATTTAAAGAGTAT | 9873 |
rs531946103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112249 | ATGTTTGAAGGATAT[C/T]TTCACCAGACATACC | 9873 |
rs531982335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912771 | GCTTTTCCTTGCTGA[C/G]AGACTTTCTATTACA | 9873 |
rs531998128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979866 | CAGAGGGCAACTAGT[A/C]CAGATTAGAAGAATG | 9873 |
rs532002504 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952394 | CAGTGGCACTATTTC[A/G]GCTCACTGCAACTTC | 9873 |
rs532008935 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119296 | CAACAGAGCGAGACT[C/T]TGCCTCAAAAAAAAA | 9873 |
rs532015360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089326 | TCAGAACTCTCATAG[C/T]GTTAGTGGAAAAGTA | 9873 |
rs532019916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906495 | TTAGTCATGAAGTCT[C/T]TGCCCATGCCTATGT | 9873 |
rs532036057 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023698 | AAAACTTAGGTTCAC[-/A]AAAAAAACCTGAGCA | 9873 |
rs532038989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129058 | TTGTATTTTTAGTAG[A/C]GACGAGATTTCACCA | 9873 |
rs532041123 | snp | A/C | 0.000633692 | 0.0177889 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842583 | GGAGCAATTTTCTTT[A/C]AACATCTTTTAATTC | 9873 |
rs532056725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006337 | AAATTCTTGATTTCC[C/T]TAAAATCTGTTCTGG | 9873 |
rs532075125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898901 | TGCCCAGCTAGTTTT[C/G]TGTATTATTATTATT | 9873 |
rs532084552 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970811 | ATTTTGGGGTTAGGT[A/T]TACAAAATGGGACAA | 9873 |
rs532111771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899693 | GTGAGCCGTGATTAT[A/G]CCATTGCACTTCAGT | 9873 |
rs532123067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051842 | TTTTTATATAATAGA[C/T]CTTCAGGATGCTAAC | 9873 |
rs532131127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136321 | TCTCAAGCTGGGCAC[A/G]GTGGCCTGACGGTAG | 9873 |
rs532134813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059065 | TTGTTGAACTGTACT[A/C]AATTCAACAAACATG | 9873 |
rs532151718 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998662 | TAAAAGAATATAGGA[C/T]TTAAAAAGTAAGAAG | 9873 |
rs532156469 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124093 | CCATAAAAAAGGATG[C/T]GTTCACGTCCTTTGT | 9873 |
rs532164440 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099713 | TCTTCTGCACCCTCG[G/T]TCTGGTTGGGGCTGT | 9873 |
rs532185611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051231 | GAGGAGGGAAAATCA[A/G]TTGAACCCAGGGGAT | 9873 |
rs532189122 | in-del | -/TT | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121159 | GTCTCACTCTCTCTC[-/TT]ATACACATACACATA | 9873 |
rs532197272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890936 | AAGAGGCTTTTAATA[C/T]AGAAAGCAGCAAAAT | 9873 |
rs532201423 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131978 | ATCAGTCACTGACAT[C/G]CATATATTTCCACAA | 9873 |
rs532212130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991005 | GAAGAATCAAACAGA[C/T]GCAATAAAAAATGAT | 9873 |
rs532215122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998056 | TAATAAACTTGTTAA[A/T]TATTCAGATTGAAGT | 9873 |
rs532216436 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048294 | ACACATATGGGACCC[-/A]AAAGTTACCTCTGAT | 9873 |
rs532221007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037189 | ACAGAGAGTTCCCAT[C/G]TATCACTTGCCCCCA | 9873 |
rs532229523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907310 | TTACTCTTTTCCTAA[C/T]TGAATACCCTTTATT | 9873 |
rs532252822 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936919 | CTAGTAAGTCCAATG[C/T]ATGGACTTCCTTGGA | 9873 |
rs532254077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943360 | CTTAATTCAACTATA[A/G]TTAGGATTAACTGAG | 9873 |
rs532255997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043305 | TTAAATCACTAAAAG[G/T]CTCGGTCAAGTAGTG | 9873 |
rs532264528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951053 | GACACAGGTTTAGCC[A/G]GGCCATGAGAGAAAG | 9873 |
rs532267928 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949800 | ATTTGGGTTGTTTCC[A/G]CCTTTGGATTGTTAT | 9873 |
rs532279197 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051534 | TGTCTCTGAATGAGG[C/T]AGAGGTAGTAAACCA | 9873 |
rs532284655 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929184 | GCCGCTATAAACATA[C/T]GTGTGCGTGTGTCTT | 9873 |
rs532286163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029752 | CCACCTTTTGAGAAC[C/T]ACACATTGAAAATTA | 9873 |
rs532286213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037784 | TAGGAGTCCTCATTA[C/T]CTTGTAACCCTCCAA | 9873 |
rs532300823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909805 | TCTGCCCGGCCGCCC[C/T]GTCTGAGAAGTGAGG | 9873 |
rs532321028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928463 | TCCCAAATAAGTTAT[A/T]CTCTTGGCCTAGAAT | 9873 |
rs532321128 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142190 | AGCAGGGGCGCGAGG[A/G]TCTCAGCCGGCCGGG | 9873 |
rs532324640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135624 | AAGAAAGTAGACTCT[A/G]CTTGTCTACTGCTGA | 9873 |
rs532326716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844777 | AACTCCAAGTTACAC[A/G]AACAAAAATAAGGCA | 9873 |
rs532339581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920876 | GATTTTTGTATTTCC[A/G]TATCAACCTAGCATT | 9873 |
rs532348821 | snp | G/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837323 | AAAAATTTCTTCAGT[G/T]ATCACCTTACTTTTG | 9873 |
rs532360674 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883057 | AGGTAATGGGAAAAG[C/T]ATACTCTTTAAAATA | 9873 |
rs532363635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092288 | GTACACCACCACACC[C/T]GGCTAATTTTTTAAG | 9873 |
rs532369397 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911726 | ACATGTGCACAATGT[G/T]CAGGTTAGTTACATA | 9873 |
rs532403832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869896 | AGTTTAAAAACTTTC[A/G]TAACTCCTGACTGTC | 9873 |
rs532405717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983020 | AAGAAAGGGGCCGGG[C/T]GCGGTGGCTCATGCC | 9873 |
rs532432702 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904512 | CAATATTCTTTCATC[C/T]TTAAGCCCACCTACC | 9873 |
rs532436870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023552 | ATGCTAGTGAGGACG[C/G]AGAGTTACAGAGTAC | 9873 |
rs532468809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967462 | ATTACTAATATATGC[C/T]ACAACATGAATGAAC | 9873 |
rs532479174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075470 | GAACTAGAACCTTCA[G/T]GCATTGCAAAACGAG | 9873 |
rs532483588 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884321 | GATGTTAGGAAATAC[A/T]TGTTTATTCTTCATA | 9873 |
rs532495339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015703 | CGAAAACACAGCAGA[A/G]GAAAGAAGTAATTCT | 9873 |
rs532504465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929953 | GAAGGGTCTGAGCTA[C/T]AAAAGCAGACTCCAG | 9873 |
rs532510595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023010 | ACAACAAAACAACAA[A/G]AACCCTTGACACATA | 9873 |
rs532523149 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877185 | AGAGATGGGGTTTTG[C/T]CACTTCAGTTTTTTT | 9873 |
rs532530828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112302 | CTTTGGCACTTTAAA[C/T]ATGTCATGTCACTCT | 9873 |
rs532534938 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975600 | CCTTACACATTGTAC[A/G]CATGCATCAAAATAT | 9873 |
rs532544135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913761 | TTTCAACAGTCAAGC[C/T]GAGAGCCAAATTACT | 9873 |
rs532548262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853326 | AAATCTCACCTTATA[C/T]GATACACAGAAAAAA | 9873 |
rs532549331 | snp | A/G | 0.000475384 | 0.0154099 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841601 | GCAGCAAAGGGAAGC[A/G]AGGTTACCCGGTGCT | 9873 |
rs532559076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061460 | CCAGTGAGACAGAAC[A/G]ATTCACTTCCCCTGG | 9873 |
rs532565385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951959 | TCTTTCACTTACAAG[A/G]TAACTTTCAGAATCT | 9873 |
rs532576441 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898683 | TTCTGGCTCTAATGC[C/T]TATTAGCTGAGTGAC | 9873 |
rs532594097 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889252 | AGGCGTGAGCCACCG[C/T]GCCCGGCTATAATTA | 9873 |
rs532595495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118682 | TGATTTCTATTTTCA[C/T]TGCATGTGATCAGAG | 9873 |
rs532605776 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048588 | TTTCATTCTGGGACC[C/T]CATCTGAAGTAGTTA | 9873 |
rs532605809 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944869 | GACCTCTTCAAGGAG[A/C]ACTACAAACCACTGC | 9873 |
rs532611203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900850 | TAAACTCTGGAACTA[C/T]ATCATAAACTCCCTT | 9873 |
rs532636253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024179 | TAAAAAAAATCTACC[A/G]GTGGTTGGGGGAACC | 9873 |
rs532646530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967893 | TCAGGAGATTGAGAC[C/T]ATCCTGGCTAACGCG | 9873 |
rs532681104 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101491 | GTCACCTAGGCTGGA[C/G]TGCAGTGGTATGATC | 9873 |
rs532688795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119218 | GAAGAGGGAAGATTG[C/T]TTTGAGTCTGGGAGG | 9873 |
rs532690060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945468 | AAAAGCTAGGCAATA[C/T]CATTCAGGACATAGG | 9873 |
rs532693093 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861087 | TAGAAAAGAGAAAAA[C/T]GAGGGAAAAATCAAT | 9873 |
rs532701254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108374 | TCTTCACTTTGTTGA[C/T]TGTTTCCTTTGCTGT | 9873 |
rs532704645 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861989 | GGTTTACCAGGAATG[G/T]GAAGCTGGTTTAATA | 9873 |
rs532712637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007745 | TGCACAGAACTCAAT[A/G]TGCACACACATACAC | 9873 |
rs532715976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045175 | TGAAAAAATGCTCAT[C/G]ATCACTGGCCATCAG | 9873 |
rs532716225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093806 | GACAGGGTTCTTCCA[C/T]GTTGGTCAGGCTGAT | 9873 |
rs532731599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052901 | GCCCAGACTGGAGAG[C/T]AGTGGTGTGGTGTCA | 9873 |
rs532737797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992907 | GCCAAAATTGACAAA[A/T]AGGATCTAATTAAAC | 9873 |
rs532750173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126855 | CCAGCCTGACCAACA[G/T]GGCAAAACCCTATCT | 9873 |
rs532751127 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866271 | TTTTGTTTTGTTTTG[-/T]TTTTTTTTGTTTTTT | 9873 |
rs532757633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026301 | TAAATGAAATATTCT[G/T]TATGAGGACTATAGT | 9873 |
rs532762898 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085581 | ACGCAACCACATTTA[A/C]GGGAGAAATTGAAAA | 9873 |
rs532773028 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999468 | GGAACTACAGGTGCA[C/T]GCCACCACACCTGGC | 9873 |
rs532775042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008497 | ACAGAAATAAAGACA[A/G]GGAAAAAGACTGCTT | 9873 |
rs532777737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969903 | ACCTGACCCTCATTA[C/T]TACAGGAATAGGGGA | 9873 |
rs532793153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901602 | CAGTGCACAGCACTG[C/G]AAATGTAGTAAGTGA | 9873 |
rs532808642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925500 | CACTGCACCCCAGCC[C/T]GGGCAACAGAGCGAG | 9873 |
rs532816971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125934 | AACTACATTTCACAA[C/T]AGAAACAATGTTTTA | 9873 |
rs532833994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916133 | CTTAATACGTGGGTG[A/G]TAAAATAATGTGTAC | 9873 |
rs532837551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000309 | ACTTCCACAAGAAAA[C/T]TTTAATTACTTATTA | 9873 |
rs532855468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054566 | AATCTGGAAGACCCT[A/G]AAGAATCCCAGACAC | 9873 |
rs532863624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134055 | ATGATATACAGTCAC[A/T]TCATGTAACTTACAT | 9873 |
rs532865645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846426 | ACCTCGCGATTCGCC[C/T]GCCTTGGCCCCGCAA | 9873 |
rs532878992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061494 | GGGGTGCTGAAGCCA[A/G]GGAGCCAAGTGGTAT | 9873 |
rs532891586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072350 | AATCTATGTCCCCAA[A/G]AGTACTAACATTTAA | 9873 |
rs532897471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116393 | GGCATCACAGTTATA[A/C]AAGATTAATAAAATG | 9873 |
rs532906827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033797 | GTATTCTTGGATAAG[A/G]CACCAAGCTAACTAG | 9873 |
rs532938778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019790 | TGCTTAAATTAACTG[A/G]TTTCCTCTATACTTT | 9873 |
rs532947045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111274 | TAGCTCTAATATTTG[C/T]TTTACATATCTGGGT | 9873 |
rs532949265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064654 | TTATATCAGTGGTGA[C/T]ATCCTGTGGGATATT | 9873 |
rs532986924 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864854 | GCTGATGGGGTTGCT[C/G]GCAGCAATCTAACAG | 9873 |
rs532986931 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035254 | TTGGAGCGCAGTGGC[A/G]CGATCTTGGCTCACT | 9873 |
rs532993695 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955660 | TCTCCTATGACCCAG[A/G]AAACTCCAAGGGATT | 9873 |
rs532999070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002887 | ATGTAATTGTTTATT[A/G]ACATCTGTCCCTCTC | 9873 |
rs533016520 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070467 | CTCGTTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 9873 |
rs533020945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970687 | CTGCCACAGCCTGCC[A/G]ACATCCCACTCACAT | 9873 |
rs533025944 | in-del | -/ATTAA | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972191 | TCTCCAGCCCAAGAC[-/ATTAA]ATTAAACTCTGAAAT | 9873 |
rs533028967 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916711 | TCAGATATGTGATGT[A/G]CAAATATTTTCTCTC | 9873 |
rs533039155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898596 | AAAACTCAAAAATAA[A/C]ACCTGGTTGCATCCC | 9873 |
rs533066975 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861030 | AATCCAAATTGAACA[A/G]AAGAAAAGAAATAAT | 9873 |
rs533079572 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948687 | TTTTTTTTTTTTGAG[A/C]GGCAGTCTCGCTCTG | 9873 |
rs533087423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841395 | TTTTGCCCTTCAGGC[A/G]AATATGTAGGTTTCT | 9873 |
rs533103598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856443 | ACAATTCTATAGCAC[C/T]GTATACATGTATCAA | 9873 |
rs533104700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850026 | ATGACTATCTTTCGC[A/G]CTTACATTTTTCATG | 9873 |
rs533109433 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097384 | TTATTTTATTTATTT[A/T]TTTTTTTTTTTTGCA | 9873 |
rs533112709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011218 | TCTCAACAATATGTG[C/T]AGGTGCCAGCCATGG | 9873 |
rs533115476 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964882 | GCAAGTTCTGCCTCC[C/T]GGGTTCACGCCATTC | 9873 |
rs533122051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910142 | GGAGCACCTCTGCCC[A/G]GCTGCCCCATCTGGG | 9873 |
rs533136889 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095648 | TCCAAAACTCAAAGC[A/G]GGAGTACCTTTGTAC | 9873 |
rs533147842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842133 | TTTAAAGGCTGTTTC[C/T]CTGTGATGAACTAAG | 9873 |
rs533159367 | snp | A/G | 0.0011165 | 0.0236009 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843101 | ACTCCAGGGCAATAC[A/G]GTTTAGGTCAAACGT | 9873 |
rs533160856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049581 | GGAGATATACCTAAT[A/G]CTAGATGACACGTTA | 9873 |
rs533162646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115658 | ATTTATTTTAAGAAA[C/T]TGGTTCATGCAATTG | 9873 |
rs533170314 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849235 | TCCAACATTCATGTA[A/G]TCATCCCACAATTAT | 9873 |
rs533171004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904341 | TTGTCCTCAAAACTA[C/T]TAACCTTTTTGTTTT | 9873 |
rs533175797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988659 | GATATTCAGACACCA[C/T]AGCAGTGACTTCAGG | 9873 |
rs533176736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997306 | AACTCTAGGAGTAAG[C/T]GAAACAGAATAGCCC | 9873 |
rs533184686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089714 | TAGAATTTCATTTAT[A/T]CAAAGTGTCTAGAAT | 9873 |
rs533185742 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970955 | GAAGGTCTGAGTCAA[C/T]AGGCAGCATTAATGA | 9873 |
rs533185785 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012065 | CAGTGTACAAAAATA[C/T]ACTTATGTTCATACA | 9873 |
rs533215358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942252 | CCATCTCTCACCATA[C/T]GACATGCAGGCTTCC | 9873 |
rs533225974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122748 | GAAAAAAAGTCTCTA[C/T]TGGACTCTGTGAAAT | 9873 |
rs533230588 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889464 | ACTGCTGAGTGTTGA[G/T]AAAGTACAGAAAAAA | 9873 |
rs533233667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003367 | TTTTAAATGAATACA[C/T]AGTAACAGCAGCAGA | 9873 |
rs533253568 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042237 | GCTGAGATTATTTTT[-/A]AACTCTGGTGAAAGA | 9873 |
rs533255933 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130517 | TAAACTATCTTCACC[C/T]GCCTTGGGCTGCAAT | 9873 |
rs533259600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905251 | CCTGTGCCTGTGTCC[C/T]GCTCTCCTTTTTTTC | 9873 |
rs533264556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896586 | AAGAAGGCCGTTGAT[A/G]AGATCCTCTTTGTGG | 9873 |
rs533296766 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981191 | CTCATTTTTAAGGGG[A/C]AGGAGGGACCAACCC | 9873 |
rs533298815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874052 | ACCCTGAACTGCATA[C/T]GATCTGGTGCTGCCC | 9873 |
rs533301644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897092 | CAGCTCTCAGCCTCC[C/T]AAAGTGCTGGGATTA | 9873 |
rs533312460 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882069 | AGAATGGCATGAAGC[C/T]GGGAGGAGGAGCTTG | 9873 |
rs533314341 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065453 | AACCGGCACAAGACA[A/C]GGATGCCCTCTCTCA | 9873 |
rs533315283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941718 | ACAAGGGTGCAAGGA[C/T]AGGCACTTTCATACA | 9873 |
rs533329136 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139340 | TTGCTTCACCATGCA[A/G]ATCATCTTCCATTCT | 9873 |
rs533349413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130037 | AGGCACCCGCCACCA[C/T]GCCCAGCTAATTTTT | 9873 |
rs533351942 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041988 | TTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT | 9873 |
rs533367930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083293 | CAGTGGCTCATGCCT[A/G]TAATCCCAACACTTT | 9873 |
rs533389359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897888 | CATTTCAGCAAAAAA[A/G]ATGTATTTTACTTTT | 9873 |
rs533398139 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850479 | CCTCCTCAGCCTCCC[G/T]AGTAGCTGGGACTAC | 9873 |
rs533416955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137498 | GTATACAGTATCTCA[C/T]CCAAGAAAAAATAAG | 9873 |
rs533424594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866471 | GACAGCGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 9873 |
rs533425274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881565 | GGAAAGGAAATCAGT[C/G]TATCAAAGTCATACC | 9873 |
rs533432399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114751 | AGGGCCTGATGACTC[C/T]GCCCAGTGCCCTATC | 9873 |
rs533442972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966969 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACGAGG | 9873 |
rs533448684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021722 | AATAAAACTTAAAAA[A/G]AAAGCTCATTCATGA | 9873 |
rs533474976 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035256 | GGAGCGCAGTGGCGC[C/G]ATCTTGGCTCACTTG | 9873 |
rs533505105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082602 | CTGACAAAGCCTAAA[A/T]GAGTCATGCCCCAAT | 9873 |
rs533510785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092496 | GTCTATGAATTGACT[A/G]TGGAGCTCCTTGAGA | 9873 |
rs533542578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028294 | ACATCTTGCAACAGC[A/G]TGCCCTGGATGTGAG | 9873 |
rs533570910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918398 | TTACCGAATTGCCCT[C/G]TCTAGGACTTCCAGT | 9873 |
rs533571332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084684 | CTGGCATGGGCCAAC[C/G]TGCTTAGCCAGTACA | 9873 |
rs533582961 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953040 | CTGAAAGTGCAAAGA[A/G]TAAGAGATATTTATG | 9873 |
rs533609416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020922 | CTCTGTCACCCAGGC[G/T]GGAAGGCAGTGGCAT | 9873 |
rs533610344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928039 | CATAGTGAAGATAAA[A/G]GATAAAGGTAAAGGA | 9873 |
rs533610814 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042415 | CCATCCCATTGTTCT[A/G]TGTGTCTGTATTTAT | 9873 |
rs533613078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974956 | AAGAGCTAGAGACGA[C/T]AGAGAAACCAGAAGA | 9873 |
rs533619595 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006004 | CCTCGAACCCCTGGA[A/C]TCAAGTGGTCCTCCC | 9873 |
rs533635586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065793 | TAGGAATCCAACTTA[C/T]AAGGGATGTGAAGGA | 9873 |
rs533635857 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062837 | TGAAAGGGACAAGGA[C/G]AATGGAACCCAGTTG | 9873 |
rs533645490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965084 | ATGAGCCACCGCGCC[C/T]GGCCAATCATTTTAC | 9873 |
rs533646222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868888 | CTTAGCTTTTACTTT[G/T]TAAGTTACCTTTTTT | 9873 |
rs533647628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875399 | ACAGAGTCTCGCTCT[A/G]CTGCCCAGGCTAGAG | 9873 |
rs533671263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921208 | ATTTGCCAACCACAG[A/G]AACAATTTATCTTCC | 9873 |
rs533674142 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925265 | TAATCAGGATCATTT[A/C]TGATTATAGATATTT | 9873 |
rs533679357 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956784 | GGAAACTTCAGACCA[C/T]AGCACTATTGCATAG | 9873 |
rs533679504 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039286 | ACTTTGGGAAGCAGA[C/G]GTGGGCGGATCACTT | 9873 |
rs533693584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066410 | CTAGAAGAAAACCTA[A/G]GCAATACCATTCAGG | 9873 |
rs533698299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966906 | GAACCCTGATTATGA[C/G]TTAAGAAAGTGGCCG | 9873 |
rs533699668 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866348 | GATTTTGGCTCCCTG[A/C]AACCTCTGCCTCCCG | 9873 |
rs533708487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905860 | ACATTTGGGTTGGCT[C/T]CAAGTCTTTGCTATT | 9873 |
rs533715107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860699 | AATATACAAAATTTA[C/G]CTGGGCGTGGTGGTG | 9873 |
rs533718393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113847 | TGAAAACTTGTAGTG[G/T]TACTGCCTTAGTGGT | 9873 |
rs533720545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858166 | ATACAGAGGAAGACA[A/G]CTCCTCAATATTTAC | 9873 |
rs533744758 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037347 | ACAGTCTATGTGTCT[A/G]GACAAACATATAGTG | 9873 |
rs533746944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108452 | GGTTGCCTGTGCTTG[C/T]GTAGTATTACTCAAG | 9873 |
rs533767455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015938 | ATGCCATAAAGGAAG[A/C]TCTTTTCCTTAAAAT | 9873 |
rs533774418 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968891 | AAGATATTTCTATAA[A/G]TTGGTAAACAAAACA | 9873 |
rs533786150 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009243 | GCTCACGCCTGTAAT[A/C]CCAGCAGTTTGGGAG | 9873 |
rs533810677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061251 | GGAAGCCATGAGGGA[C/T]TGAGCCTGAAGAACT | 9873 |
rs533825702 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144343 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 9873 |
rs533826868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008202 | AAATTAGCAGGGCAT[A/G]GTGATGCACACCTGT | 9873 |
rs533832822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118911 | CCTCTCTTAGACACA[C/T]ACTACACAACATGTA | 9873 |
rs533846255 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108559 | GATTTAAGTTTTTTT[G/T]TTTGTTTGTTTTTTG | 9873 |
rs533847674 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075726 | AGACTGACGCATGAG[A/T]ATTTCTTGAACCCAG | 9873 |
rs533869258 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114589 | CCAAGACCCACAGCG[C/T]ACTAACTAGGTATTG | 9873 |
rs533889960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008919 | AATATATTATTATTA[C/T]CAGTTCATAGTCAAG | 9873 |
rs533896582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999699 | AAGAGAAAAGCACCA[G/T]AGGTAGTTAAACTCT | 9873 |
rs533902588 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892077 | GAATGAATTTGTAGG[A/G]AGTAGCTAGATGAGA | 9873 |
rs533906106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901130 | GACATCGTGGCTCAC[A/G]TCCGTAATGCCAGCA | 9873 |
rs533913568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067588 | CCCCAATATCATCAT[A/G]TTCAAGATCCCTGAA | 9873 |
rs533913668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076671 | ACATACTTAAGATTG[A/G]TGAATCATTAATGGT | 9873 |
rs533930190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045024 | GCAGTGAGCCGAGAT[C/T]GCTCCACTGCACTCC | 9873 |
rs533930803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922071 | TTAATAATAAATGGA[C/T]AAAAGATACAGATTG | 9873 |
rs533935060 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944978 | TGGCCATACTGCCCA[A/G]GGTAAATTATAGATT | 9873 |
rs533936062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976126 | GCAATAGTTTTTTGT[C/T]TGTTTGTTTTAGTTT | 9873 |
rs533937035 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136784 | CCTGTAATCCTAGCA[A/C/T]TTTGGGAGGCCGAGG | 9873 |
rs533939719 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901865 | ATTAATTCTATTCTG[G/T]TTTTTTTTTTGTTTG | 9873 |
rs533952669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023709 | TTCACAAAAAAACCT[A/G]AGCACAAATGCTTCT | 9873 |
rs533976227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967655 | GGGTATAGAGCTTTT[C/T]TGGGGGATAACAGAA | 9873 |
rs533990020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045323 | ACACTGTTGGTGGGA[A/C]TGTAAACTAGTTCAA | 9873 |
rs533992897 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937419 | GCAAGAAATATAAAG[A/C]CTTAGTGTTAATTCA | 9873 |
rs534013800 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965118 | TTAATTCAAAGGTCT[C/T]TGATAGATCCCCATT | 9873 |
rs534034368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885314 | ACGGATCTGCTACAA[A/T]GGTTTTAGCATACTA | 9873 |
rs534042465 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143243 | GAGGGAAGCCTTTCT[A/G]AAGGTTACACAGCAG | 9873 |
rs534052492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039100 | TATTTTTATCTGCAA[C/T]CAGTTTCAAACTGGA | 9873 |
rs534073045 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861626 | CTAGCAAACCAGTTC[C/T]AATCAATATATAGAA | 9873 |
rs534084759 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931125 | TTTTGAAAAGGAGTC[A/G]CGCTGTGTCACCTAG | 9873 |
rs534112908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039790 | TTTGATGACTTTAAG[C/T]GTTTAATTATTCCAC | 9873 |
rs534115663 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032015 | AAATTATGGTCATCA[A/G]TATGCTGCAATGTTA | 9873 |
rs534118928 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070919 | GAATTTAGTTTGATT[C/T]AGAAGTAAAACCTAG | 9873 |
rs534119326 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907442 | TGCTTCCAGTTTTTG[C/T]CCATTCAGTATAATA | 9873 |
rs534120556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061638 | GTGGGGAGAGACGTC[C/T]GCCATTGCTGAGGCT | 9873 |
rs534138795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853488 | GGCGCAATCTTGACT[C/T]ACTGCAACCTCCGCC | 9873 |
rs534146231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100943 | ACCCTTTTCTCAGAG[A/C]TCTCCTCACACAGAC | 9873 |
rs534167204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931948 | TTATCAGACTGACTT[A/G]TATTTTGACCAGACA | 9873 |
rs534172212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128206 | GAATACAAATAATTT[A/C]TATGGAGTCTCTAAT | 9873 |
rs534175803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024730 | TGGGAGAAAATACTG[C/T]AAACTACGCATCCCA | 9873 |
rs534176646 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068135 | TCGCACAACACATGG[G/T]AATTATGGGAACTAC | 9873 |
rs534180467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952866 | AGATATATAATAAAG[A/C]AATAAAAGCCTACTC | 9873 |
rs534183315 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879639 | TTCACAAGATGGCCT[A/T]AACAGTAGTTTATAC | 9873 |
rs534183485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968673 | ATGGAATTTCAGAAG[C/T]CCTGCAAACTTTCTC | 9873 |
rs534187544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879008 | CCAGCTACTTGGGAA[A/G]CTGAGGCAGGGGAAC | 9873 |
rs534187953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053977 | GTATTTTACAAAAAT[A/G]TCCATCTACAAATTT | 9873 |
rs534201542 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992110 | ACAAGCATTCTTATA[A/C]ACCAATAACAGACAA | 9873 |
rs534202395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924167 | GCTGGACTCAAACTT[C/T]TGGGTTCCAGTAATC | 9873 |
rs534207807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915295 | ACTTTTACACTGTTG[G/T]TAGGAGTGTAAATTA | 9873 |
rs534213450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101901 | GAATATATTGTGTCT[A/C]TGTATGAAAACAGAT | 9873 |
rs534227638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862503 | TAGCACCAAAATTAT[A/G]AAATAGGGGTAAGTC | 9873 |
rs534232169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945643 | GAATATTTTTGCAAT[C/T]TACTCATCTGACAAA | 9873 |
rs534264524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070395 | ACGCCAGTCGTAAAG[A/T]AGATACTTGATAAAT | 9873 |
rs534273525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012435 | TGGAAGATGCTTGGG[A/C]AATGATATTCTTTAT | 9873 |
rs534275616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094103 | GTAATCCCAGCTACC[C/T]GGGAGGCTGAGGCAA | 9873 |
rs534279141 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993484 | TTGTGGCACTATTCA[A/C]AATAGGAAAGACTTG | 9873 |
rs534283861 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079842 | TCTATAAATGGGCTC[A/G]ATTTTCCCAAGCAGA | 9873 |
rs534321714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057739 | CTATTAATCAAGCTC[A/C]GTCCCTAACCCTTTA | 9873 |
rs534329053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905412 | AAGCATTTATCCTTA[C/T]TTTGTATTACAAAAA | 9873 |
rs534336500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885929 | TGGAGGTGGGGTTAC[C/T]GGGGTTTCTCCAGCC | 9873 |
rs534341308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094885 | TTTAACGAGGCAAGC[A/G]GAACGAACAACTGAA | 9873 |
rs534349038 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999031 | CAGAAAAGCAGAGCT[A/C]ATGGATGGAAAGAAA | 9873 |
rs534350789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850847 | GTAATCCAAGCACTT[C/T]GGGAGGCCAAGGTAG | 9873 |
rs534370356 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851780 | CAAAACAAGAAAAAA[A/G]ATAAAGTTCGTGAAG | 9873 |
rs534374468 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142342 | CGCCCCCGCCCGCCC[A/G]GGAGGAGGAAGGTGG | 9873 |
rs534386716 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948901 | GGATCTCCTGACCTC[A/G]TGATCTGCCCACCTC | 9873 |
rs534414596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897269 | ATATCTGTGGGTTCT[A/G]TATCTGTGGATTCAA | 9873 |
rs534415870 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986354 | AGCTGGGACTACAGG[C/T]GCCTGCCACCACGCC | 9873 |
rs534416537 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884429 | AGTGAAACCTCACAG[C/T]AACAGGCCCAGAGGT | 9873 |
rs534417652 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087235 | AAAAAAATAAAAATT[A/T]GTAAAAATAGTCAAA | 9873 |
rs534424408 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941863 | ATCTTAAGGAAGTTA[A/T]CAAAGAGGTGTATTA | 9873 |
rs534424731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042171 | ACTTCAGGTGATCCA[C/T]CCACCTCAGCCTCCC | 9873 |
rs534428882 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845173 | CGTCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 9873 |
rs534451930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978012 | TCATGTCCTTTGTAG[G/T]GACATGGATGAAGCT | 9873 |
rs534479343 | in-del | -/ACACACAC | 0.301932 | 0.244547 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051869 | TAACACGGTATATAA[-/ACACACAC]ACACACACACACACA | 9873 |
rs534486427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870387 | TATGTGTTCAGTAAC[C/G]TTTTTTGAATAAATA | 9873 |
rs534487215 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078932 | ATTATGTTGTCAGGC[A/C/T]GGTCTGAAACTCCTG | 9873 |
rs534487895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042624 | TTGATAGAGACTGCA[C/T]TGAATCTGTTGATTG | 9873 |
rs534502446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934249 | TTTAAATGAGCAAAA[C/T]ACAAGAATGTTCTTT | 9873 |
rs534513157 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044971 | GTTACTCAGCAGGCT[A/G]AGGCAAGAGAATCAC | 9873 |
rs534518504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025457 | GAACACATGCACACA[A/T]AGAGGGGAACAACAG | 9873 |
rs534521263 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995798 | ATAACTTGAATATAA[G/T]AATACAAATAAAAGT | 9873 |
rs534525978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081990 | GGCGGATCACCTAAG[A/G]TCAGCAGTTCGAGAC | 9873 |
rs534533658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090926 | AATCACGCTTCATTC[C/T]CCTTTCTTCTCCTCC | 9873 |
rs534546160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871087 | GGAATAACTGCTTAT[C/T]CTTTAGCCCTTGTTC | 9873 |
rs534553396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035388 | TGCCCGGCTGTTCTC[A/G]AACTCCTAAGCTCAA | 9873 |
rs534554069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969331 | GCTTTAAGTTATTTA[C/T]ATCAGGAATAAAAAT | 9873 |
rs534557131 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849594 | GCAAGTGAAAGACGT[C/G]AAGTCAGAGCCTAAA | 9873 |
rs534580226 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033061 | TGGGGGGCTGAGGCA[G/T]GCGGATCATGAGGTC | 9873 |
rs534583845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082855 | TTATCTTTGTACATG[A/G]AAGAATAGTTATTAA | 9873 |
rs534590867 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948196 | TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCATGT | 9873 |
rs534593494 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060152 | GAGTTAGTCACCCAA[C/T]AGATTCATTGAATGA | 9873 |
rs534614813 | in-del | -/A | 0.212122 | 0.247114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087705 | GCGAGGCTTTGTCTC[-/A]AAAAAAAAAAAAAAA | 9873 |
rs534616987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995559 | AAGTACAAAAATCAG[C/G]CAGGTGTGGTGGCAA | 9873 |
rs534618293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896759 | AGCAATTAGGGGGAA[A/G]ATACTAAAAAAAAAA | 9873 |
rs534623034 | snp | A/G | 2.20053e-05 | 0.00331695 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841557 | CAGTGGAGGCAGGGA[A/G]GCGTGTGGCTTGGGG | 9873 |
rs534623152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850187 | CGTGCCTCAGTCTCC[C/T]GAATAGCTGGGATTA | 9873 |
rs534657681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972487 | TAGGGAGTGGGGAAA[A/C]CACACAAAGAGGAAA | 9873 |
rs534661050 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093787 | TTTTTGTATTTTTAG[C/T]AGAGACAGGGTTCTT | 9873 |
rs534669883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918736 | AACATTGTTATTTTC[C/T]GAATTCTTTTTTTAA | 9873 |
rs534683844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965183 | CCATTCATATAACTT[C/T]CTAGAATCCAGCCTC | 9873 |
rs534717818 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024866 | AAAAACAGACATACA[C/T]GCAGCCAACAATCAA | 9873 |
rs534725172 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090683 | AAACTGGCAGTATTA[A/G]TAGAAGAAAGACCTT | 9873 |
rs534730845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73140007 | GACAAACAGAAGTCC[G/T]TGAACTATTTACTAT | 9873 |
rs534742598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842525 | CCGGTGAGGGTAAGG[A/C]AGAGACTGCAGCCCA | 9873 |
rs534744630 | snp | G/T | 2.41882e-05 | 0.00347757 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988937 | TTATTTGCATAATAA[G/T]TTTCTCAGAAATGTT | 9873 |
rs534758975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066654 | TACAAGAAAAAAAAA[A/C]CCATCAAAAAGTAGG | 9873 |
rs534765147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957039 | TTTTTTTTTCTTCTT[C/T]TTTTTTATTATACTT | 9873 |
rs534770188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115848 | TTGAGGGTAGCCTCC[C/T]TTACTTAAAGTCAAC | 9873 |
rs534781809 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889462 | ACACTGCTGAGTGTT[-/G]AGAAAGTACAGAAAA | 9873 |
rs534802178 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958006 | TGATAAATGTATACA[A/G]TATCTGAATCTACAG | 9873 |
rs534817448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123094 | AATTAACATGAACTA[C/T]ATATACATTAAAGAA | 9873 |
rs534834300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059422 | AAAACATTGTGTCAG[A/G]TAAGTGTTAGCCATC | 9873 |
rs534844100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851685 | GAGGCAGAGGTTGCA[C/G]TGAGCCGAGATTGTG | 9873 |
rs534844135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843746 | AAAAACTCAAGAAAC[C/T]GAATCCTCAAGAGGC | 9873 |
rs534850132 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038083 | TATTAAAAACAAAAC[C/T]ATCTATCACTAAAAA | 9873 |
rs534850451 | in-del | -/GTAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035206 | TATGTATGTATGTAC[-/GTAC]TAAGACAAGGTCTCG | 9873 |
rs534857599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028094 | GGAGCCCCCACACAG[A/G]ATGCTCACAGGGGCA | 9873 |
rs534871459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882214 | TTGGGAGGCCAAGGC[A/G]GGTGGATCATGAGGT | 9873 |
rs534872513 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020315 | TAGAAGGGTGCTCTA[C/T]GGCTCTAGCACAGGT | 9873 |
rs534874131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122185 | TAAAAGGCAAAAAAA[A/G]AAAATGTAGCTCAAA | 9873 |
rs534880533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971865 | AGTTTGTGGTGATTT[G/T]TTACATAGCAACGGA | 9873 |
rs534885275 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992811 | ATAAAAACCCTAGAA[G/T]AAAAGCTAGGCAATA | 9873 |
rs534914343 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099170 | CAGTAAGCTATGACT[A/G]TGCCACTGCACTCCA | 9873 |
rs534922304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866026 | CCTGCTCAGTTCAAA[C/G]TCAGATGGTATATGG | 9873 |
rs534933902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130109 | TCAATCTCCTGATCT[C/T]GTGATCCGCCCGCCT | 9873 |
rs534936697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917881 | TGACAGAGTGAGACC[C/T]TGTCTCAAATTAAAA | 9873 |
rs534946475 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062861 | CCAGTTGGAAAACAC[A/T]CTTCAGCGTATTATC | 9873 |
rs534982356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990703 | CTCTGGGACACATTC[A/G]AAGCAGTGTGTACAG | 9873 |
rs534983873 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021316 | TCGACCTAAATGGCC[A/G]TCAATGGTAAAGTGG | 9873 |
rs534984287 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097550 | ATTGGTGTTAATTCA[A/T]CATTAACTGTTTGGT | 9873 |
rs534985286 | in-del | -/TAT | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030873 | AAATCCTGAATACAA[-/TAT]TATTAACTATAGTCC | 9873 |
rs535008647 | snp | A/G | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141445 | ACGGGCGGGGCTGGC[A/G]ACAAGCGGCTGGAGG | 9873 |
rs535016278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116647 | CTGGGCACAAGCTCC[C/T]GCGTCAGCCTCCCAA | 9873 |
rs535017455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137758 | ACACAGGGGCATGAA[C/T]GTAGAGTGCACAGTT | 9873 |
rs535020118 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093659 | CAGGCTGGAGTGCAA[C/T]GACGCGGTCTTGGCT | 9873 |
rs535024364 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991134 | TGATAAATTCCTCGA[A/C]ACATACACCCTCCCA | 9873 |
rs535045704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848682 | CATAGTCTATTTAAC[A/G]CAGGGATGTGCCTGG | 9873 |
rs535049150 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996432 | ATAAATGTGAAAGAT[-/A]ACGGACAAAAGTATG | 9873 |
rs535049164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013456 | CAAAGGACAGACAAC[A/G]TATCTTCTAGCCTCT | 9873 |
rs535061023 | in-del | -/AG | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069933 | AATATGTAAAAAAAC[-/AG]AGTCACAGAAAATTA | 9873 |
rs535073098 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107051 | TATATATATATATAT[A/T]TTTTTAAATGGAGTC | 9873 |
rs535080657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058721 | CTGCCTCAGCCTCCC[A/G]AGTACCTGGCTAATT | 9873 |
rs535100226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913097 | AACAACCAGATCTCA[G/T]GAGGACTCACTCACT | 9873 |
rs535114734 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978382 | GAATAGACATTTCTC[-/A]AAAAAAAGTCATATA | 9873 |
rs535128494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969320 | AATTTAATTTGGCTT[C/T]AAGTTATTTATATCA | 9873 |
rs535130383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960740 | TTGGGAGTTGATGTG[G/T]AGAAAGGGTATGGGG | 9873 |
rs535137763 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983581 | AAAAATATATTTTTA[A/G]TAGAAATATTCTTTT | 9873 |
rs535148509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844281 | CAAAGAACTATGTAC[A/G]TGAATTTGATGATAG | 9873 |
rs535151290 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052282 | AAATTTTGTGTAACG[G/T]TATATTCTGATGGTG | 9873 |
rs535175487 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061726 | GGTGGAGCCCACTGC[A/C]GCTCAGCAAGGCTGC | 9873 |
rs535181135 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881885 | GGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG | 9873 |
rs535190236 | in-del | -/AG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853438 | GATTTTTTTGGAGAC[-/AG]AGTCTCGCTCTGTTG | 9873 |
rs535198563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906869 | GCACGATGTCTCCAG[C/T]TTTGTTCTTTTTGCT | 9873 |
rs535216386 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126040 | ATATGTTTGCTTGTT[G/T]CAAGACAAAAGAATT | 9873 |
rs535219087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051473 | TTACACCTAATTTAC[A/G]AACAGAAAAAGTTTA | 9873 |
rs535232139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855119 | TCTCTACTAAAAATA[C/T]AAAATTAGCCGGGTG | 9873 |
rs535238260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953197 | AGGAACATTCTTTGA[G/T]AAATGGTCTTGAGAA | 9873 |
rs535239364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109929 | AATTTTATTAAATGC[C/T]TTTTGAGCATCAATT | 9873 |
rs535255634 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955367 | AAGGTATGGAAGAAG[A/G]CATGTGAGGCTTCCA | 9873 |
rs535268681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902172 | GAGCCACAGCGCACG[A/G]CCTACTCTGGTTAAA | 9873 |
rs535287057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847838 | GCTGAGATTACAGGC[A/G]CCCGCCACCACGCCC | 9873 |
rs535287684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052122 | AATGCAAAGATAGTA[C/T]GGCATTTCCTTTGGT | 9873 |
rs535297459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110453 | ATTATGCATTCCTTC[C/T]AGATTTTTCAATTTA | 9873 |
rs535298276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043424 | TTTCTATTTGCTTAA[G/T]TGTTCTTTTCCATTT | 9873 |
rs535300892 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960414 | TGCTCTAGTCTGCTG[C/T]TCCTTTGGATTTAAA | 9873 |
rs535321413 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952743 | AAAGATAAATGAATA[C/T]TTACAGAACACCTAC | 9873 |
rs535331284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943937 | AATCATTATTCATTG[G/T]GATGCTGCCAACTTT | 9873 |
rs535352958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044290 | ATGAATATTTCCAAA[G/T]TCAGAGGCTGAGTGT | 9873 |
rs535360805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891211 | TGTTCAAATTAGAGG[C/G]ATGAGCCAGTACACC | 9873 |
rs535363287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002298 | CCAGATGAATCGGTT[C/T]AGATGGAAATAGTCA | 9873 |
rs535380527 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018151 | CATCTGTGGTCTGTC[A/G]GAGCCCCTCCAAGTT | 9873 |
rs535390549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946934 | ACAAGGCAGCACCAG[A/G]TGCCCCTCTTTGTGG | 9873 |
rs535393290 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886650 | GAGTAGATAAAAGTG[C/T]GTGCACAGGTCCTCC | 9873 |
rs535395266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986493 | GGATTACAGGCGTGA[A/G]CCACCGTGCCCGGCC | 9873 |
rs535397222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994642 | GTGGTGGTGGGCGCC[C/T]GTAGTCCCAGCTACT | 9873 |
rs535427955 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941753 | TTTCAGAAGTATATA[C/T]TGATATAATCTTTTC | 9873 |
rs535431281 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066664 | AAAAAACCATCAAAA[A/G]GTAGGCAAAGGATAT | 9873 |
rs535448576 | in-del | -/AA | 0.0202498 | 0.0985639 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049874 | CACAAAAGGACCATA[-/AA]AAAAAAATTGTTTTC | 9873 |
rs535472673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025265 | AGTGATAGACTGGAT[A/T]AAGAAAATGTGGTAT | 9873 |
rs535475838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879209 | CGGCATTAGTATAGG[G/T]CTAATTTCTAATTTA | 9873 |
rs535481608 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991545 | ATCCCCGGGATGCAA[C/G]GCTGGTTCAACATAC | 9873 |
rs535490507 | snp | G/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839719 | ACTCATTTTTGCTGA[G/T]TTTTGGGGATCTGGG | 9873 |
rs535501981 | snp | A/G | 1.67346e-05 | 0.00289258 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887621 | TGTTTTTTACTTTTC[A/G]TCTTCCTTAAGTGAT | 9873 |
rs535509399 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070314 | ACTCTGTTTTACTGA[A/T]AACATTCCAGCACTA | 9873 |
rs535515722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862327 | TATTTGCAGGTGACA[C/T]GGTTATATAGAAAAT | 9873 |
rs535520766 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029103 | ACCATAAATATAATG[A/G]TGTAGTACACTAAAA | 9873 |
rs535530613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909137 | CCTGCCTTGGGCTCC[C/T]GTGATTCTCCTGCCT | 9873 |
rs535536608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121860 | GATTAGGGATAAGCC[C/T]ACAAAACTGCATTTT | 9873 |
rs535550142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138494 | GCCTTCCTGAACTGC[C/T]TCTGAAAATGTATTA | 9873 |
rs535554819 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026545 | AATATATAAAACAGA[G/T]ATACAGTGCTCTAAA | 9873 |
rs535571105 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971065 | GTTATCCCTACTGAC[C/T]CCCCTGCCCAAAGTA | 9873 |
rs535571815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062371 | TTCCAAAAGCCAAAA[C/T]GCCTCTTCTCCTCCA | 9873 |
rs535579271 | snp | C/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843266 | GCTCAGGAGGCTGTT[C/T]GAGGTGGGAAACTGT | 9873 |
rs535579437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025703 | ATCTCCTTGGAATTA[A/G]TTTGTAGAATTATAA | 9873 |
rs535585082 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031709 | CAAGCCTTCTGACTC[C/G]AAGGCCAGTCCACAC | 9873 |
rs535590195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009937 | TCCAGTATCTGGATG[A/T]CTAAATCTCGTTAGA | 9873 |
rs535601571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979961 | ATGTCCAGGAAATAC[A/G]AAAAGAACATAAAAT | 9873 |
rs535609622 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092651 | TTTTCAGACTCTTCA[C/T]AAATTTGATTAATAG | 9873 |
rs535621824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027333 | CTTTAACAGAGAGAC[G/T]GGCAGCATTTTGCCC | 9873 |
rs535634212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873277 | GAGGCTGCAGTGAAC[A/C]GAGATCGCGCCACTG | 9873 |
rs535634634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925655 | GAGATAATAACTGAC[A/G]CACGTATCCCAGGGT | 9873 |
rs535638082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137610 | CTTCATCTGAGGGAG[A/G]ATGCCAGAACCATGT | 9873 |
rs535643735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054975 | TGAGACTGGGTAGTT[C/T]ATAAAAAGAGGTTTA | 9873 |
rs535657685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902926 | CAAGAAGATAGTTTT[A/T]ACACAAAAAGCTATT | 9873 |
rs535678446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019319 | AGGCTTTGTTATCAC[C/T]ACAGAGAAATTGGAC | 9873 |
rs535696086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909913 | AGGAGCACCTCTGCC[C/T]GGCTGCCCATCATCT | 9873 |
rs535699650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046322 | GAAAAGCCTTATGAA[A/C]TGATTTTAAAAAGAA | 9873 |
rs535707780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055542 | ATGATAGCAGAAAGT[A/C]ATCAAAAGATACTGA | 9873 |
rs535709425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946235 | AAAATGATGAGTTCA[C/T]GTCCTTTGTAAGGAC | 9873 |
rs535724003 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916932 | TTTTGAGTTAATTTT[G/T]TGAGGTAAGGGTTCA | 9873 |
rs535733540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910344 | AGAGACAGCGACCAT[C/T]GAGAACGGGCCATGA | 9873 |
rs535753859 | in-del | -/T | 0.499968 | 0.00399348 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138605 | TATCTTGCACAGGAA[-/T]TTTTTTTTTTTTTTT | 9873 |
rs535756388 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144311 | ACAAGGTCAAGAGAT[C/G/T]GAGGCCATCCTGGCT | 9873 |
rs535767304 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996550 | ATTTTGAAAAATGTA[A/G]TAATTCTCATAATCC | 9873 |
rs535774961 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139453 | CATCCCTCTAGTAAG[A/G]AAGATACTGATTTTC | 9873 |
rs535775957 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035845 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGACTA | 9873 |
rs535777373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840100 | TCCAGCCTCCTAATC[A/G]CTCCCTATATCCTTT | 9873 |
rs535779758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115785 | CTTCCAGATACCTCA[A/G]TTTTGTTCCTAAGGC | 9873 |
rs535795725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096229 | ATTTAAAATGAATTT[G/T]TAAACTTCTTGTATT | 9873 |
rs535814433 | in-del | -/ATAA | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975628 | TATCACACATACACT[-/ATAA]ATATATAGTTATTAT | 9873 |
rs535816248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956376 | TATGCTAAGGCTGGT[C/G]AGTGGAGGTCTGACA | 9873 |
rs535818127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856788 | AGAATCACAGACTTA[C/T]GATTCTATTGTTTTC | 9873 |
rs535818573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040793 | TGATTACACTAATCC[A/G]ACTGTGCTATAAAAT | 9873 |
rs535830314 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044692 | TTAAAATTAGGCAAA[C/T]GCTGGGTAAATACTA | 9873 |
rs535837470 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122868 | TTTACAAAGAATCTA[C/G]AAGATATGCAGATTA | 9873 |
rs535852400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043346 | TTATCAGTTTCCATA[A/C]GCAAGTATTTATCAT | 9873 |
rs535858494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088078 | ATTCCTTGCTATGTT[C/T]CCTAGGCTGGTCCTG | 9873 |
rs535863561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882398 | TGATGGTTATCAGAA[A/G]CTGGGAAGGATTATG | 9873 |
rs535868114 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119401 | AAATCTATATACTTT[A/G]AAATTTTTATGTGCT | 9873 |
rs535872334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990543 | AACTAGAACTCAGGA[C/T]TAAGAAACTCACTCA | 9873 |
rs535875216 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977081 | AGGTGCCCACCACCA[C/T]ACCTGGCTAATTTTT | 9873 |
rs535880493 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932868 | ACAAATAATAACACC[A/T]ATCAGAATTCGCATG | 9873 |
rs535881950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033403 | AGATGTAAATGGGAC[A/T]AGTTTTAGTGCAAAG | 9873 |
rs535904708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979003 | GCTGGGACTACAAGT[A/G]CATGCCTCCACACAC | 9873 |
rs535912198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036383 | ATTTCACAACGTTAT[A/G]TCGGTCTTTGGAGTC | 9873 |
rs535918457 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946982 | ATCTATGCAATAGCT[C/T]ACCCAGCTACCCAAG | 9873 |
rs535918546 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908857 | TGGGGTTTCACCATG[A/T]TGCCCAGGCTGGTCT | 9873 |
rs535931002 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080153 | AATAAAAATACTAGA[C/T]GGGTATGGTGGCATG | 9873 |
rs535967235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924876 | TTAAGTCTGAATAAA[C/T]TTCCTGTATCAGGAC | 9873 |
rs535979353 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943559 | GAAGGAAATTGAAGA[G/T]AATGACAGGTGAGAC | 9873 |
rs535987753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928524 | CTTAAATGATAATGA[C/T]GGTTAACACAGGCAA | 9873 |
rs535992534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970338 | GAGTAAAAATACTTA[A/C]AATTCTAATGTATGA | 9873 |
rs535998585 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851250 | CTAAACATACCATTG[A/G]TCTAGCAATTCCGCT | 9873 |
rs536002745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916381 | GTAGTAGCATGATCA[G/T]AGCCTGCTGCAGCTT | 9873 |
rs536004401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876028 | AAACCAGCAAAAGAA[A/G]TGACTAGTTGGCTTG | 9873 |
rs536006242 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983077 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 9873 |
rs536016137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025930 | TACTGATATGCTCCA[C/T]GTTTTGACTAAAAAA | 9873 |
rs536028861 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056618 | CATTCATTCATTCAT[C/T]AAATAAACATTCACC | 9873 |
rs536070044 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921067 | GCCAGTTCTCACTCT[A/C]CCTGACAAAAAAAAA | 9873 |
rs536071071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023083 | CCTCAATATAAAGCA[C/T]AAAACTATGAAACAT | 9873 |
rs536083947 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846460 | GCTGGGATTACAGGC[A/G]TGAGCTACCGTGCCC | 9873 |
rs536091438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133703 | CAGGAGGCTGAGGCA[A/G]AATTGCATGAACCCA | 9873 |
rs536091703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141736 | CGGCAAGTCGGTGAC[A/T]AGCCCAAGACGAGGG | 9873 |
rs536108895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963581 | AGCCCCCAACCTTTT[C/T]GGCACCAGGGACCAG | 9873 |
rs536110246 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090248 | TTTTTTTTTTTGAGA[C/G]GGAGTCTCGCTCTGT | 9873 |
rs536126017 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913822 | AAAAACCAAAAAAAA[A/C]CCAAAAAAAAAACAA | 9873 |
rs536130827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067444 | GTAACAAAACTGCGC[A/G]TTCTGCACATGTATC | 9873 |
rs536134703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011421 | TGCCCCAGCACCACT[C/T]GCTCCCCAGCAGCAC | 9873 |
rs536143368 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881126 | CTTGCAAATTATTCA[A/T]GCAACAAGGGACTAA | 9873 |
rs536152620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73141169 | AGCCGGGTGCATCCG[C/T]CACTCCCACCCTGGT | 9873 |
rs536165787 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124489 | GGCCAGGCGCAGTGG[C/T]TCACACCTGTAATCC | 9873 |
rs536183104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056940 | ACAAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 9873 |
rs536188863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060316 | ACCTATTTATTATTA[C/T]TATCTGTCACCAGCA | 9873 |
rs536195235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955229 | CACCTTTCTTAGGGT[C/T]GATTAGTTTGCTATA | 9873 |
rs536196576 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878380 | TATCCCTAGCTCTAA[C/T]AACAAAGAAAAGATA | 9873 |
rs536204985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006909 | TTTGAAACCAAATGT[A/G]TCTGGCTCCCAAACC | 9873 |
rs536218703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907815 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 9873 |
rs536231730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951496 | CTTGGCATTTAGCTC[A/G]ATAAATGTTTGCTCT | 9873 |
rs536242589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935508 | CTTAAAATTAAATCA[C/T]GAAATTCTACAGTCT | 9873 |
rs536243062 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121411 | GGAGGATACCAGAAA[A/C]GGCCTCATAAAGCAT | 9873 |
rs536248653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908472 | AACTGTTTTCCATAG[C/T]GGTTGTACTAATTTA | 9873 |
rs536252962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836370 | CCAGTGGTCACATCC[A/G]GCAAGGGGACTTCAG | 9873 |
rs536259680 | snp | A/G | 0.00207507 | 0.0321439 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900317 | ATCCACCAGTTGGGC[A/G]GCTTTTAAACTCTGC | 9873 |
rs536269781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845225 | CAGCAGTTTGAGACC[A/G]GCCTGGGCAACATGG | 9873 |
rs536278733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936234 | AGAGAATTTCATCTA[A/T]CTCCCTTGTAAGCCT | 9873 |
rs536305754 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052937 | CTGCAACCACCGCCT[C/T]CTAGGTTCAGGTGAT | 9873 |
rs536318914 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903464 | GACCTCGTGATCCAC[C/T]GGCCTCGGCCTCCTA | 9873 |
rs536326793 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092389 | CAGTGATTCTTCCAC[C/G]TCAGCCTCCCAAAGT | 9873 |
rs536335769 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083822 | ACACCTTCAAATACT[G/T]CCTGGTTAAGATATG | 9873 |
rs536343102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891781 | TCTGAGTCGTAGCTA[C/T]ATCTGAAAACTAGTG | 9873 |
rs536351777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037248 | TCCCCCACCACAGTG[C/G]TACATTTACAATGGA | 9873 |
rs536366192 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126147 | AAGTTCGAGACCAGG[C/T]TGGCCAACATGGTGA | 9873 |
rs536368812 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873350 | AAAAAAAAATGAATC[C/T]TTTCATGTGCTTATT | 9873 |
rs536378676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973988 | AGTGCAAATGAAGGA[A/G]CAATTAATTGTGAAA | 9873 |
rs536383328 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837767 | ACGGAAATGTCAGGG[G/T]AGTGGGACCTGGAAG | 9873 |
rs536394849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074947 | TGGGGAGGGAGGGAG[A/G]CAGGGAAAGAAAGAC | 9873 |
rs536408751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929246 | TATACCCAGTAATGG[C/G]ATGGCTAGGTCAAAT | 9873 |
rs536424453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038412 | AGGGACCTTATAATT[C/T]ATCCAGTCGAATCCT | 9873 |
rs536427759 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045245 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 9873 |
rs536440846 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857637 | TTTTTTTAGTAGAGA[C/T]GGGGGTTTCACTATG | 9873 |
rs536446936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984329 | CAAGAATAAAGGTAA[A/C]CACGTGCGGAAAACA | 9873 |
rs536462267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075590 | GGAGGCCAAGGAGGA[C/T]GGATCACTTGAGGTC | 9873 |
rs536469445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085639 | CAGGTTCACAAAAGA[A/C]TTCAGAAGACCTGAT | 9873 |
rs536473040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930389 | CCAATCTGTCCCAAA[A/G]TGCAATTCTTGTTTT | 9873 |
rs536475536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938665 | GGTTTGTCTGGAGAG[A/G]GTCAATTTTCATCAT | 9873 |
rs536489058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031089 | TGGATGGGTTCATCC[A/G]GAATATGTTAAGTGA | 9873 |
rs536495707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921013 | TTTGGACACTGTCAT[G/T]TGAAAATGGATATCC | 9873 |
rs536502829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966641 | ACATTCAACAGATAT[A/G]TATGTCAGTTACTGT | 9873 |
rs536503422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116829 | GGCATGAGCCACAGC[A/G]CCTGGCCCATATCTC | 9873 |
rs536513005 | in-del | -/T | 0.475702 | 0.107512 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924441 | GCCACCACACCCGGC[-/T]TTTTTTTTTTTTTTG | 9873 |
rs536526506 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096156 | GAAAAACATGGTAGC[-/AGA]AGGACACCCATGAGC | 9873 |
rs536530708 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868723 | AACAAACAAACAAAC[A/C]AAGAAACTATATAAC | 9873 |
rs536531555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086235 | CCAACATGGCAAAAC[C/T]CCGTCTCTACTAAAA | 9873 |
rs536534070 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976355 | GGAGTGCTGTGGCAG[A/G]ATCATAGCTCACTGT | 9873 |
rs536534966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859744 | TGGTCAGTACATATA[G/T]GTGAAGAAATTACCC | 9873 |
rs536536678 | snp | A/G | | | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72844233 | TGGAACTGCTACCAG[A/G]GGGCTCCCATGGACA | 9873 |
rs536537665 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005601 | TCTCTTCTCTAACTA[-/C]ATTCACTCTGTTGAA | 9873 |
rs536541581 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923738 | AGAGATCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 9873 |
rs536552479 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077232 | CAAACAACCCAATTT[-/A]AAAAAAAAATCAATA | 9873 |
rs536564510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124137 | AAGCTGGAAACCATC[A/T]CTCTGAGCAAACTAT | 9873 |
rs536566298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922386 | ATATGTATATTTACT[C/G]AACAGCAGTGACAGA | 9873 |
rs536570292 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014913 | CAGTGACATGATTTC[G/T]GCTCAATGCAACCTC | 9873 |
rs536584411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067992 | TGGTGACAGACACGA[C/G]AGAATAAGAACCAAG | 9873 |
rs536596095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077768 | AGCTGGGAGAGAGGG[A/T]TTATAAGGACACACA | 9873 |
rs536605873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852726 | ACTATTTATACTAGC[A/G]AAGACATGAAATCAA | 9873 |
rs536621200 | snp | A/G | 3.40379e-05 | 0.00412526 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73015822 | ACCTGTAATCATTCC[A/G]ATCATCAGCTTTTAC | 9873 |
rs536622414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963412 | CTAAGTGAGGCATAC[A/C]GAAGGGAAATAATTT | 9873 |
rs536629149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959673 | TAAATTGCTAAGATA[G/T]ACATTTCAACGCACC | 9873 |
rs536639343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083534 | AGCCTCGCAACAAAG[C/T]GAGACTCCATCTCAG | 9873 |
rs536644451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064055 | GTAAAACACTCCTCA[C/G]CAAATGCAAAAGAAT | 9873 |
rs536645992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061174 | AGGCGAGCCGAAGCA[C/G]GGTGGGGGGTCACCT | 9873 |
rs536650004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910281 | CTGGGAAGTGAGGAG[C/T]GCCTTTGTCCGGCCG | 9873 |
rs536659622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999011 | TGTTAGTGAGTGAAG[C/T]CATTCAGAAAAGCAG | 9873 |
rs536682583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104013 | AAAAATACAAATAAA[C/T]GTTTTCTGTTATTAA | 9873 |
rs536685531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007923 | ATTTATTATTTCTGA[C/T]GACTATGTGTGGCTA | 9873 |
rs536706211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056794 | AATAAAATCCATAGA[C/T]TGACAAGGCCGGGCG | 9873 |
rs536711612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955143 | CTGCTCCCCACTTCA[A/G]ATGCTAATTGGAAGT | 9873 |
rs536714040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952112 | ACAGGAAGAGCACCC[A/G]TGAGTTTAATGCTTG | 9873 |
rs536741543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900977 | CGTGCCTTCTCATTT[C/T]GCAGAAGTTAAATTT | 9873 |
rs536742322 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912555 | GATTTTTGCATTAAT[G/T]TTCATCAGGGATACT | 9873 |
rs536743175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999616 | TGAGCCACCACACCC[A/G]GCCTTATCAAACATT | 9873 |
rs536760081 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112497 | AATCTGCTTGGTGTT[C/T]TATATGCTTCTTATA | 9873 |
rs536764701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124608 | TGAAAATACAAAAAT[C/T]AGCTGGGCATGATGG | 9873 |
rs536777655 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896637 | CAAGGGACTTTTAGT[C/G]ATCAATCCAATAAGG | 9873 |
rs536781522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892832 | GATGGTCTCGATCTC[C/T]TGACCTCGTGATCCA | 9873 |
rs536789665 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846131 | CTTGAGACTGAGCGC[A/G]TATGTTTTCCCAGAC | 9873 |
rs536804504 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105072 | CTTATCCTACCTGAC[G/T]TGACAATAACTCTAT | 9873 |
rs536810542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101664 | GTAGTCTGGAACTCC[C/T]GACTTCAAACGATCC | 9873 |
rs536823220 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962596 | GATATGAACTAAATT[-/C]CCCCCTTTTTTTTTT | 9873 |
rs536830004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73141117 | GCCTCGGCCCCTGGG[A/G]AAGCTGGGGAAGGGC | 9873 |
rs536847464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117386 | TGATTTATATTTTAT[C/T]ATTTTTCCATCCTAT | 9873 |
rs536855795 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885256 | ATTATTTTATGCTAA[C/T]AGTAAAATTAATTAA | 9873 |
rs536862038 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993414 | CCATTACTGGGTATA[C/T]ACCCAAAGGATTATA | 9873 |
rs536870937 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097616 | TCTTGTGAGGTGTTC[C/T]TTTTTTTTTTTTTTT | 9873 |
rs536872746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093921 | ATGAATGTTAAGAAT[A/G]AAGATAGGACTGGGT | 9873 |
rs536873250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941809 | AAAGTATTAACCAAT[A/C]TTTGTTTTTGACCAG | 9873 |
rs536882780 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876855 | AGCATTATTATTATA[C/T]ATACGTCCAGGATTT | 9873 |
rs536885732 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018843 | ACTATTTTAAGAGAA[A/G]TATGTGTGGGTATTC | 9873 |
rs536891878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042119 | TTTAGTAGAGACAGG[G/T]TTTCACTGTGTTGGC | 9873 |
rs536902106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877887 | GGCACATGTCTGTAG[C/G]CCCAGCTATTCGGGA | 9873 |
rs536919270 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017385 | ACTTATTTCTATACA[C/T]GTAACTAAAAAGAAC | 9873 |
rs536920803 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059342 | TTGTTTCCTTTTTAA[A/C]AAAGGAATTTTAAAA | 9873 |
rs536922238 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026297 | CAGATAAATGAAATA[A/T]TCTGTATGAGGACTA | 9873 |
rs536934717 | snp | G/T | 0.00399679 | 0.0445244 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089971 | GTAATTAAAATAGCT[G/T]GGTAATGGAACATAA | 9873 |
rs536937294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988849 | CACATGTAGGTCAAA[C/T]GAAACCACCACTACC | 9873 |
rs536945774 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988961 | AAATGTTAAAACACA[C/T]ACTTTGCCTCGATGT | 9873 |
rs536958271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031899 | TAGATGCTGGGGGAA[C/T]AGCAATAAACATTAT | 9873 |
rs536966927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132286 | CCACTAATAACAGTA[C/G]CTACCAATGCTAAAT | 9873 |
rs536970723 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049105 | GGATGGTGAAGATCT[A/G]ATTTAATAGCAAGAT | 9873 |
rs536975494 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980706 | ATATATAATGTATGT[A/G]TGTATATATATGTAT | 9873 |
rs536996122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927082 | AATTCACAAGCACAA[A/C]ACAAATGTATTTCAG | 9873 |
rs537014460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110761 | GGTACATCATTAGGT[A/T]ATCTAGCTGAAGATT | 9873 |
rs537025108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010578 | TAGATCTATGGTGTT[A/G]TTTGGTAGGGCCCTT | 9873 |
rs537027346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954458 | CGATCCTTCCCCTTC[A/G]GCCTCCCAAAGTGTT | 9873 |
rs537035053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118225 | TTGGGAGGCTGAGGC[A/G]GGAAAATTGCTTGGA | 9873 |
rs537046022 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087749 | TTTAGTGCAGCCTAA[A/G]TGTATAGTGTAATAA | 9873 |
rs537047640 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090436 | TTCACCGTTTTAGCC[A/G]GGATGGTCTCGATCT | 9873 |
rs537051749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903893 | CTACTGCTTCCCTCC[C/T]CCTCACTCCACCAAC | 9873 |
rs537077957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002462 | CAACCAATGGAACTT[A/G]CAATGTAAACTCACC | 9873 |
rs537099358 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956826 | TGATTTCATAGTGGA[-/A]AAAAAAAAAAAACCA | 9873 |
rs537102526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972399 | TTCTTTCCAAACTAT[A/G]TTTCAAGGTGCCCTA | 9873 |
rs537108060 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125464 | AATCCCAGCACTTTG[C/G]GAGGCCAAAGAAGGG | 9873 |
rs537111698 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865591 | CCCTTCCTTCACAAC[A/G]AGAACAGCCCTTCTT | 9873 |
rs537119549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073803 | GAAGACCACATAAAA[G/T]CAAATAATAAAAACT | 9873 |
rs537133734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865953 | TATGAGGAGGGAGAC[C/G]AAGTTTTGTTCATCT | 9873 |
rs537140801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994845 | GCTTTTAAAAAATTG[A/G]CATATAATTCACATA | 9873 |
rs537146791 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121804 | AGTGATTATTAAAAC[A/C]TGGATTGCTGGGCTC | 9873 |
rs537169920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922012 | TGACATATGATATCT[A/T]CTGCCTATGAGAAAA | 9873 |
rs537185229 | snp | G/T | 3.32049e-05 | 0.00407448 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840895 | TCGCAGTTTGCCATA[G/T]GAGGTCTCAGGAGTA | 9873 |
rs537208541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858415 | AATGTGGTACATATA[C/T]ACCATGGAATACTAT | 9873 |
rs537219545 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013303 | AGAATTTCTTTTACC[A/C]AACTGTCTGCCTGGA | 9873 |
rs537230922 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041473 | GATTTTCATTTCCCT[G/T]ATGATTAGTGATGCT | 9873 |
rs537238949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123807 | GTGCTGGCCAACTGA[C/T]TCTTACTTAAAAGGG | 9873 |
rs537249544 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998193 | ATTATCTTGCTAGAA[G/T]ATTTTTATATTGTTC | 9873 |
rs537249981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905902 | CGCAATAAACATATG[C/T]GTGCATGTGTCTTTA | 9873 |
rs537253580 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988063 | TTTCACAAGTTGCTT[A/G]TAAGGTTGCTTACAT | 9873 |
rs537265037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996546 | AATAATTTTGAAAAA[C/T]GTAATAATTCTCATA | 9873 |
rs537272117 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851088 | GCTGGGGCGACACAG[C/T]GTGACTCTGTCTCAA | 9873 |
rs537284292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004952 | TTCCCACCACATTTG[C/T]CAAACTCCTTGTCTC | 9873 |
rs537284682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034402 | CAAACATGCAAAAAC[A/G]TTCCTCTTCCTGAAA | 9873 |
rs537296963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880942 | TAGTACAAGAAAACA[C/T]AGGGGAAATGCTTCT | 9873 |
rs537297128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889183 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT | 9873 |
rs537302481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123299 | CCTCTCCTGCAGTAT[C/T]TCCTAGCCAAGCCAG | 9873 |
rs537335584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898472 | TCAAAATTCCTAATT[A/C]AAACTATAAAATTCA | 9873 |
rs537343867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106789 | ACATGCTGGACAGGT[C/T]TGTAGCCTAGGAACA | 9873 |
rs537345941 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977654 | CAGTTAGAATGGCAA[A/T]CACTAAAAAGTCAGG | 9873 |
rs537347926 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997538 | TTAAAAGAGACCTAC[A/G]GTAATTCAGATAGTG | 9873 |
rs537367065 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969923 | GGAATAGGGGACTGG[G/T]CTCAGAAAAAGACTT | 9873 |
rs537375965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926024 | GTCCCTGCTGGCTTG[A/G]GGATATCTGTTCCCG | 9873 |
rs537392309 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873418 | ATTCAGACCCTTTTC[C/G]CATTTTTAAGTTGAG | 9873 |
rs537422359 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143430 | GCTCCTTAACAGGCT[A/G]GGTGAGCTCGGCTTC | 9873 |
rs537425530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028026 | TCTGCTGCAGGGGCA[C/G]AGCCCTCATGGAGAA | 9873 |
rs537446855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935409 | AAACAAACTCTTCTT[C/T]TCTGAGAGCAACGGG | 9873 |
rs537450960 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076736 | AAAGTAACCAGCAAG[G/T]GATAGCAGGTGGGAA | 9873 |
rs537459780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072854 | CACTAACTTCTTGTA[C/T]AGTATGCCCAAGTCT | 9873 |
rs537466573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976185 | TACAGACAGAGAAAG[A/T]TATATTCAGTATCTG | 9873 |
rs537483012 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913309 | AGTCTCAGTCTGTTG[C/T]CCAGGATGAAGTGCA | 9873 |
rs537487715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023819 | AATGGAATAGTACTT[A/G]GCAATTAAAAGAAAC | 9873 |
rs537490047 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103942 | CTTTTCTTTTGCAAT[G/T]TCTGAAACAAGGTGC | 9873 |
rs537500297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020254 | GTAGACACTAGGAAA[C/T]GGACTGATGGCTTAA | 9873 |
rs537502928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977068 | TAGCTGGGACTACAG[C/G]TGCCCACCACCACAC | 9873 |
rs537509961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971905 | TAACTGCAAAGGAAC[A/G]AGAGATAAAAGTTTG | 9873 |
rs537514329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068199 | AAACCATATCAGTAC[A/C]CCAAATAAATGAAGA | 9873 |
rs537515240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113890 | CCAGAAGAATTCTCT[A/G]TATTACTAGGCAGAG | 9873 |
rs537519645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918508 | TTATTGAATATGACA[C/T]TGGTTGATGCTATCA | 9873 |
rs537533765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869589 | GTCATCCTTGCATAG[C/G]GGCCATGCTAATCTT | 9873 |
rs537545331 | snp | C/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839382 | TAAGCAATATCAGAT[C/T]TGCGAAAAGATGACT | 9873 |
rs537580103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113260 | CAAAATAGCTATTTC[A/G]AATTATCTGTCTGAA | 9873 |
rs537585168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959925 | ATATTTCAATGCACT[C/G]ACCTCAGTCTAACTT | 9873 |
rs537587675 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084036 | ACAGTACTCACCTCA[C/T]AGGGATATTATAAAA | 9873 |
rs537589734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956230 | TAAACAAGCACATAA[A/G]TGGCAGAGAATAGAA | 9873 |
rs537590518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968230 | GTAGATGCTCCAAAA[C/T]TACTTTCTGAACAAA | 9873 |
rs537596679 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009687 | ACCCTTGGTTGGTAG[-/T]TTTTTTTTTCTTTCA | 9873 |
rs537598409 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861651 | ATAGAAAGGATAGGC[C/T]GGGCGCGCTGGCTCA | 9873 |
rs537599820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866748 | TTTAAATGTGCAAGT[A/G]TATTCTCATTAGAAA | 9873 |
rs537603785 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853691 | TTTAAATATGATACC[A/G]AGAGCATAGGCAACA | 9873 |
rs537605924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908623 | TTTTGATTTGCATTT[C/T]TCTGATGATTAATGA | 9873 |
rs537622292 | in-del | -/A | 0.00121507 | 0.0246182 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002598 | CATTTTAAAATAATA[-/A]AAAAAAATGAAAAAG | 9873 |
rs537623671 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008275 | ACCCAGGAGGCAGAC[A/T]TTGCAGTGGGCCAAG | 9873 |
rs537627435 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117542 | AAGTTTGTTTATATA[A/G]GGCATTCATTTTCAT | 9873 |
rs537642501 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081286 | TAAAAATACAAAAAT[C/T]AGAAGGGCATGGTGG | 9873 |
rs537643947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112658 | GTTGGTGGTGGTGTT[C/G]GTGTTGTTGAGACGG | 9873 |
rs537673525 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947931 | TGTTAACATTTTTCA[C/T]GGCACTATAATGGTA | 9873 |
rs537679341 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109197 | GGATAGCTTTGGCTA[A/G]CTATTCTGGGTCTTT | 9873 |
rs537683980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106284 | TGGTGACATAAACCT[A/G]TATCCCCAGCATTCG | 9873 |
rs537686683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009009 | TTGAGAAGCATTTAC[A/G]TAGAAAGGAATGAAA | 9873 |
rs537691420 | in-del | -/GGCCCGGGC | 0.00318978 | 0.0398085 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142100 | ACCGGGAAGGCTTGG[-/GGCCCGGGC]GGCCCGGGCGGCCCG | 9873 |
rs537699167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059180 | AAAAGTCAACCATTT[G/T]GGATGAAAGCAAAAT | 9873 |
rs537701998 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119571 | CTGGGTGCAGCCTCC[C/G]AAGTAGCTGGGACTA | 9873 |
rs537704135 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128088 | TTTCTCCAAATTATC[A/C]GAAGACTGAAGTGGT | 9873 |
rs537704909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131623 | GCACAAGGATCGCTT[C/G]AGTCTGGAAGGCAGA | 9873 |
rs537725873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983655 | CAATCTAACAAAAAT[C/T]ATGCTAAAATGTCTT | 9873 |
rs537742357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942867 | GTTCGCAGCTTCAAA[C/G]TCTTGGACTTCAGAA | 9873 |
rs537743658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098583 | ACAGTATGGTTAGTT[A/G]GAATAGAATTGATAG | 9873 |
rs537748543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101976 | TCCAAAATCTGCAGG[A/G]TAGGCCAGAAGCTGC | 9873 |
rs537749674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005879 | TGGCTTTAAAGAGTA[A/T]CAATATCCTGACTAT | 9873 |
rs537749854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950580 | TACAATTTGTTGAAA[G/T]ACTATTCTTTCCTCC | 9873 |
rs537759209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953561 | TAAAAAGTCACTCAA[C/T]AAAATATTTATCAAG | 9873 |
rs537759820 | in-del | -/CAGGGAGG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845084 | TATGTGACAGCAAAC[-/CAGGGAGG]TAGTACACTTTTAAA | 9873 |
rs537778361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899151 | TATAGGTAATGCCAT[C/T]AGAAAAATGTCTAGC | 9873 |
rs537783281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045522 | TGGAACCAACCCAGA[C/T]GTCCAACAATGATAG | 9873 |
rs537789001 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021892 | CCAGGCAACACAAGG[A/G]GACCCCTGTCTCTGT | 9873 |
rs537789217 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981305 | AAATATATGCATAAA[G/T]ACTTCAAAGTAAGTT | 9873 |
rs537805965 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862150 | ATCTACAAAAACCCT[A/G]CTGCTAACTTCATAC | 9873 |
rs537806473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001415 | TATAAAAATTAGTGA[A/C]TATTTCAGACTCTCC | 9873 |
rs537808986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930310 | ACCAATCACAGCTTG[A/C]CAGCTCCTCAAAACT | 9873 |
rs537810098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993612 | TGTCCTTTGTAGGGA[C/T]ATGGATGAAGCTGGA | 9873 |
rs537850121 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975095 | GTTCCTGGCTTATTT[C/T]ACTTAACATAATGTC | 9873 |
rs537850944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938873 | AATTCATTAGGTTTT[A/C]AAATGGTTTTTGAGT | 9873 |
rs537855130 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985715 | CTGTATGATGTAATC[G/T]TCTCCCACTCTTGGG | 9873 |
rs537862811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886003 | GGCTGTACCAAAAAC[A/G]TGCTCATATTCTCTA | 9873 |
rs537864910 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896311 | GGAAACCTGAGGAAG[C/T]TTCCGTGTTTTTCCT | 9873 |
rs537869148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840069 | ATCTTGCCACCACTT[C/G]TTTCTTGGATGCTGC | 9873 |
rs537871461 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111714 | AAGGTGATTTTCTCT[-/G]GTGGGGTGTTTTAAT | 9873 |
rs537917130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923168 | ACATTTTGTTTATTA[A/C]TCAGGTGATATAAAT | 9873 |
rs537928274 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929567 | ATGATTTGCTCCAGC[C/T]CCCTGCCTTAAATTG | 9873 |
rs537952296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024542 | TTAGAAATAAGAAGG[G/T]GAAATGAGAATGAAT | 9873 |
rs537983805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987087 | CTTCAGAATAAACAT[A/T]TCCAAAATGAAATTC | 9873 |
rs537994225 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873310 | CTCCAGCCCAGGCAA[C/T]GGTGTGAGACTCTGT | 9873 |
rs538002426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914933 | AAAATAAACTATCAA[C/T]GGAATAAAAAGGCAT | 9873 |
rs538016060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932803 | CATTCCATCTTCTGT[C/G]TTGAGCATAGGGTTT | 9873 |
rs538023579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960695 | ATCCATTCTGTTAGC[A/C]ACCAGAAAGTTCTCT | 9873 |
rs538033126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061711 | GGGAAGTTCGAACTG[A/G]GTGGAGCCCACTGCA | 9873 |
rs538033149 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025518 | GGAGGAGGGAGATAA[C/T]GAGAAAAAAATAACT | 9873 |
rs538060085 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043028 | ACTTTCTCTTTTCCT[A/T]TTTAGATGCCTTGAA | 9873 |
rs538103092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017386 | CTTATTTCTATACAC[A/G]TAACTAAAAAGAACA | 9873 |
rs538106429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054062 | GCAAATTCTAGCCTG[C/T]TGTCTGTTTCACTAA | 9873 |
rs538108245 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953028 | AAAATTTTGTTACTG[A/C]AAGTGCAAAGAATAA | 9873 |
rs538111179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961793 | TATTTTATAGAATTA[C/T]GTAACTTAGTTTATA | 9873 |
rs538121894 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936786 | TTTTATAATTTGTAT[C/T]AAAGATGATATTCTT | 9873 |
rs538124036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916286 | TTTAATTTCATTGAC[C/G]TTTTGGTACACAACT | 9873 |
rs538140660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109763 | GTGACAGTGGGCATC[C/G]TTGCCATGTTCCAGA | 9873 |
rs538149213 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945668 | GACAAAGGGCTAATA[A/T]CTAGAATCTACAATG | 9873 |
rs538172606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054939 | TTAGTCCATTCTCAC[A/G]CTGCTAAATAAAGAC | 9873 |
rs538179410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063236 | TACAGACAAGCAAAT[G/T]CTGAGGGATTTTGTC | 9873 |
rs538180041 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846811 | AAAATATGCATAATT[A/G]AGCTCTTACGGTACA | 9873 |
rs538194429 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071788 | TTTCTTGTCTTGGTG[C/T]CCACAATTATAAAAT | 9873 |
rs538195524 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839216 | TTTCAGTGTGTCTTG[G/T]GTAGAGAGTTACAAA | 9873 |
rs538204236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004823 | CTACATTTCCTTAAT[C/T]CATTCTTCACCCACC | 9873 |
rs538219218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106110 | GAGGCCAAAAGTAAA[C/T]AATTAATTTTACAAA | 9873 |
rs538247381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050460 | AAACATATATGGGAC[A/G]GGTCACCTTTATCAC | 9873 |
rs538255842 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113058 | GTGCATTTCCAAAGA[A/G]TTTATCTTCAAGCTC | 9873 |
rs538260106 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994181 | TTATTTCCATTAATG[A/C]TAGATGCTTCCCTAC | 9873 |
rs538263220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898320 | TAAAAGTCCTATAAC[C/T]TTCCTAACTATATCT | 9873 |
rs538266907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095137 | AAATTAGAAGTGTTC[C/T]TATTTCTTATTAATT | 9873 |
rs538274291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997520 | AAGAAAAACCGCAGG[C/T]GGTTAAAAGAGACCT | 9873 |
rs538279078 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939542 | TTTCTTGGTTAGAAT[G/T]TGATCACTGAGAAAA | 9873 |
rs538289411 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142233 | CGCAGCCGCGTTGTC[C/G]GCGCTCCCGGTCGGC | 9873 |
rs538292265 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942680 | TACTTTATTAAAATT[A/T]AAAAGTATTGACAAA | 9873 |
rs538299952 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889574 | AAAATTTAGCCAGGC[A/G]TAGTGGCATGTGCCT | 9873 |
rs538306150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042747 | TCATCAGTGTTTTGC[A/G]GTTTTTTGTTGTAGG | 9873 |
rs538328376 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087317 | TTTAAGCTAAATGCT[A/G]TTTCAAAAGTCAAAA | 9873 |
rs538329554 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986400 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 9873 |
rs538332936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938953 | GTAAGGATAGGGTCA[C/T]AGAAGTTTTGGTCTT | 9873 |
rs538342739 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137136 | ACCTCCTTCCTCAGG[C/T]AACTGAAGTTATCAT | 9873 |
rs538349567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989783 | AGTATCCAAAGGAGA[C/T]TGACCCCACTTTGAA | 9873 |
rs538352718 | snp | A/G | 0.000681962 | 0.0184531 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73141908 | TCAATCCTCCCCGAC[A/G]GCAGCGTTAGCAAGG | 9873 |
rs538360465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932205 | CAAACCCAACCCCTC[C/G]TCCTGATCTCCACAG | 9873 |
rs538371021 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978167 | GGCCTGTCATGGGGT[C/G]GGGGGAGCGGGGAGG | 9873 |
rs538376760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879100 | TGTGCGACAGAGTGA[A/G]ACTTTGTCTCAAAAA | 9873 |
rs538391516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087869 | CTAAGCTCCATTCAT[A/G]GCAAGTGCCCTACAC | 9873 |
rs538394421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882239 | TGAGGTCAGGAGTTC[A/G]AGACCAGCTTGGCCA | 9873 |
rs538400112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927717 | CACAGTTACTTTAGC[C/T]GACTAGGTTGAGCAT | 9873 |
rs538411213 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871221 | TCTGTGACAGCTTCT[A/G]CTTCTACTAGTCCTC | 9873 |
rs538429743 | snp | A/C/G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105192 | TAGCTCTGGTTAGGT[A/C/G/T]GGGGGAAGACTTAGG | 9873 |
rs538431746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875352 | AATATTATAAACTCT[A/G]TCTATCTATCTAGCT | 9873 |
rs538432771 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036337 | GACAAAAAAAAAAAA[A/C]CCAAGCTTCATAATC | 9873 |
rs538437034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127155 | TATATACTCCAACTT[C/G]TTTCTGTGGAACCAC | 9873 |
rs538457053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978967 | GTTCAAGCGATTCTC[A/G]TGCCTCAGCCTCCCT | 9873 |
rs538459213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969402 | TTTGCCACCTCAGTT[A/C]ATTTTTTAGAGTATG | 9873 |
rs538470774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083654 | CCTTAAGCCACGGAA[A/G]AGAAGTATACCTAGA | 9873 |
rs538490626 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877471 | GCTTTGGGTCATTTT[A/C]CAGCTCTATTAAATA | 9873 |
rs538495859 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081815 | TTGAAAGGATCAAAC[C/T]AGATAACATATATAA | 9873 |
rs538495899 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126317 | TGCACTCCAGCCTGG[C/G]CAACAGGGCAAGATT | 9873 |
rs538501968 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084879 | CCTGAGTTTAAAGAC[-/TT]TACCGTTATGTGCCA | 9873 |
rs538504727 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074602 | ATATAAAAGAAAAAA[A/T]ATATATTTCCTTAAA | 9873 |
rs538509520 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134992 | TAGAGTAGCTAGGAT[C/T]ATAGGTGTGCGCCAC | 9873 |
rs538514148 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121193 | CACACACACACACAC[A/G]CATGCACGCACACAC | 9873 |
rs538524654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919873 | ATAAAAATGTCACCC[A/T]ACCACATATTCCAAC | 9873 |
rs538541911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018501 | CTCTATAAGCTCCAT[C/T]AGGTACAGATCTTGT | 9873 |
rs538553497 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118222 | AACTTGGGAGGCTGA[A/G]GCAGGAAAATTGCTT | 9873 |
rs538561328 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943311 | ACTTTTATATTTACT[A/G]TCTACATTTAACACT | 9873 |
rs538572341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962555 | AGTGATTTTTGAGAT[A/G]TTTTTCTTCAACCAT | 9873 |
rs538585938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863866 | GGAACAACTGAAACA[C/G]TAGTACCCCGTTGAT | 9873 |
rs538586369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996754 | CAGACTACCTTTCTC[C/T]AGACTGGAAAGTGTA | 9873 |
rs538589370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066712 | AAGAAGACATTTATG[C/T]AGCCAACAGACATGA | 9873 |
rs538600133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097885 | TGCTATGTTATCCCA[C/G]TTGGGCTTAAACTCC | 9873 |
rs538602078 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989790 | AAAGGAGATTGACCC[C/T]ACTTTGAAACAAACC | 9873 |
rs538603053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965785 | GCATGTTCTTAAGTA[C/T]ATAAATAGAATCACA | 9873 |
rs538623642 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913141 | CAAGGGGGAACTCCA[A/T]CCCCGTGATTTAATT | 9873 |
rs538625295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941967 | TGGCATATTAATATG[A/C]TCAAATACTATGCAG | 9873 |
rs538633517 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72989095 | TGTCAACTGGTCCAC[A/G]CACTGTAAAATACAA | 9873 |
rs538636207 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925747 | TGCTGCCATCATGCC[-/G]GCTAGAGCAGGGAAG | 9873 |
rs538637090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949477 | AGAAAAGAAAAGAAA[A/G]GAAAGAAAAAGAAAA | 9873 |
rs538642314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958150 | GTGTTCCCACTATTT[C/T]ACAAAGGGGAAAGAT | 9873 |
rs538650356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067297 | GAGAACTCATGGACA[C/T]AGGGAGGGGAATATC | 9873 |
rs538662232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906930 | TCGGTTCCATATGAA[C/T]TTTAAAGTAGTTTTT | 9873 |
rs538680533 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866027 | CTGCTCAGTTCAAAG[G/T]CAGATGGTATATGGC | 9873 |
rs538695229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141330 | TTTTCCCTTGGGGTG[G/T]GGAGGCGGTGACTAT | 9873 |
rs538715150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060225 | TAACACCCATTCAAG[A/G]AAGTTTAAACAAATG | 9873 |
rs538719176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950781 | AGATATTTAGAGGCA[A/G]CACAGGTAGTAGTTG | 9873 |
rs538721895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091119 | TTTATGGCTGAATAA[C/T]GTTCCATTCTATGAG | 9873 |
rs538754145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107522 | ATTGTCACCCTGTTG[C/T]GCTATCAAATACTAC | 9873 |
rs538758722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943595 | TGAAGGGCACAGAAA[C/T]GGAAGTGAGAATTCC | 9873 |
rs538773321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082941 | TAATCTGGACTCCAC[G/T]AAAGGTCTAAGTAAA | 9873 |
rs538775805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044848 | GGCCGAGGCAGGTGG[A/G]TCACGAGGTCAGGAG | 9873 |
rs538786680 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052243 | CTATGAAAAATTATA[A/G]GTCAATAAACATGAT | 9873 |
rs538796613 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844502 | CCTGACAGCAGCAAT[A/C/T]CACCAGCATCAGCCA | 9873 |
rs538801990 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836821 | ACTGTAAAGAAAGCA[C/T]ATCTGCACAGAGGCT | 9873 |
rs538852904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044347 | CTTTGGGAAGCCAAG[A/G]TAGGAGTATCGCTTG | 9873 |
rs538864187 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837737 | TCCTCCACGAGCCAC[C/G]AGGTTCTTCCTTCCA | 9873 |
rs538868612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092724 | ATCTACATCCACATG[A/G]ACCAATCAAGTTTCT | 9873 |
rs538870730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021420 | CAGGGGCGTGGATGG[C/T]GCTGGAGGCTATTAA | 9873 |
rs538881241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991328 | AACTATTCCAATCAA[C/T]AGAAAAAGAGGGAAT | 9873 |
rs538884743 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965359 | GAATTTTTACTGAGC[A/G]CTCTTCTATGCACTA | 9873 |
rs538888695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875604 | GGCCTCCCAAAATGC[C/T]GGAATTAGAGGTGTC | 9873 |
rs538904335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912506 | TAATCTTTTTAATGC[A/G]TTGTTGAATTCAGTT | 9873 |
rs538935248 | snp | A/G | 4.36157e-05 | 0.00466969 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867842 | GAAAATCAACTTGTC[A/G]TATCCAAGAAAAGAA | 9873 |
rs538935439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858703 | TGAAATAATCTGTAC[A/G]ACCCCCCCATGACAC | 9873 |
rs538938176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134287 | ACCAGCTGGGGCAAC[A/T]TAGTGAAACCCTCTC | 9873 |
rs538939875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983535 | GCCAAAATTGTAGTT[A/G]ATAAAAAATTCAGGC | 9873 |
rs538951833 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865334 | TCCTCATTAAGCTAT[C/T]TTGTGCCTATGTCTC | 9873 |
rs538963585 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930480 | TAATTGGCTGGGTGC[A/G]GTGGCTCACACCTGT | 9873 |
rs538975169 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119471 | CTATGATGACAGATT[G/T]GTTTTTTAATACATA | 9873 |
rs538978545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975060 | TTAGCCAGAAAAACC[A/G]AAAAAGAACTTGGCT | 9873 |
rs538989859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117458 | AGATGAACCCACTAC[C/T]TTTCAATCTGTCCTA | 9873 |
rs538995051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085532 | TCTCTTTTTCCCCTT[C/T]TGAGAGCCAGATCTT | 9873 |
rs539003681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141802 | AGCGGTCGCCCCAGC[C/T]GCGTTCCGCGTACGC | 9873 |
rs539005121 | in-del | -/GTAC | 0.31357 | 0.241783 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035202 | TATGTATGTATGTAT[-/GTAC]GTACTAAGACAAGGT | 9873 |
rs539025049 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872865 | CCATCTGGGGAAATA[C/T]TAGACTGTTTTTCAA | 9873 |
rs539029487 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074921 | TGTCCCAAGGATGGA[C/T]GGACAGACAGTGGGG | 9873 |
rs539050431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062582 | AGAATAACCAGTGTA[A/G]AGGAGAACATAAATG | 9873 |
rs539067960 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006097 | TTTAAATAAAAATAG[A/C/T]ATCTCACTTTGTTGC | 9873 |
rs539088891 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854059 | CTGTTATATATATTT[C/T]TAAAAACCCAGAAAA | 9873 |
rs539095837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959034 | GTGTGTGTACATCCA[C/T]GCGTGCATGGGACAC | 9873 |
rs539098510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110068 | AATTTTCCTTTAATG[C/T]ATTATTGAGTTCAGT | 9873 |
rs539103385 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107860 | TGCTGATGGACACTC[-/A]AGGTTGCTTCCAAAT | 9873 |
rs539118011 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901771 | AATATTCTAAGAAAT[A/C]TGAAAGGAATTATAA | 9873 |
rs539120144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998414 | AGGTGTGGTGGCACA[C/T]GCCTGTAATCCCAGC | 9873 |
rs539129341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006730 | TTGGCATATATGTTT[A/G]ATTATTCACTTGTTT | 9873 |
rs539141703 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104919 | AATCTATATTTTACA[A/G]TATAGTTTTACACGT | 9873 |
rs539142897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909806 | CTGCCCGGCCGCCCC[A/G]TCTGAGAAGTGAGGA | 9873 |
rs539158499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946298 | GACTATCGCAAGGAC[A/T]AAAAACCAAACACCA | 9873 |
rs539160383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890665 | CTATGGAAAGTGCTT[C/T]ATATAACTTTTTTTT | 9873 |
rs539163722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852586 | CGAGAATTGCTTGAA[A/C]CTGGGAGGTGAAGGT | 9873 |
rs539175784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845193 | TGGGAGGCCAAGGTG[G/T]GTGGATCACTTGAGG | 9873 |
rs539210139 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012830 | TTTGTCTCAGAACAA[A/C]TTTGACAAACACAAA | 9873 |
rs539228777 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014389 | CCACCTCGGCCTCCC[A/G]AAGTGCTAGGATTAC | 9873 |
rs539233813 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112566 | TCTGTTGTTATCCCC[A/G]TGAATAAACTTTCTA | 9873 |
rs539243151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947020 | CTCCTTGTGTCCCAG[C/G]CTGCTTTCCCAGGCC | 9873 |
rs539246298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100513 | GGATTACAGGCATGC[A/G]CCACCACGCCTGGCT | 9873 |
rs539248194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891690 | AATAGGTTTTTGAGT[C/T]AGATAGACTTAGTTT | 9873 |
rs539250065 | snp | C/G | 0.02016 | 0.0983543 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143170 | TCCGCTGAGAGGGAG[C/G]CAAGAGAACGTTAAG | 9873 |
rs539273806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104458 | GATTTTCAGTAGAGA[C/T]GGGGTTTCACCATGT | 9873 |
rs539275786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096338 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 9873 |
rs539291451 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949058 | CACACACCATTAAGT[C/T]AATCATTTTAAAGTA | 9873 |
rs539291750 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045945 | AAAAATGGAAGGAAA[A/G]CAAAAAACATCTCTT | 9873 |
rs539298585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037406 | AGTTATTTTCACTGC[C/T]CTAAAAATCCCCTGT | 9873 |
rs539302097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991939 | GAGAAGGAAATAAAG[A/G]GTATTCAATTAGGAA | 9873 |
rs539315785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047917 | TTATTAATCCCAATA[C/T]GCAGAGGGGGAAATG | 9873 |
rs539333853 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995357 | ATAATGCTGTGTTTG[C/T]AGGTGTGAAGAGCTA | 9873 |
rs539338110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096658 | AAAGGTGCATCCTTG[G/T]GTTCTTCCTGAACTT | 9873 |
rs539341086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937634 | AGGCGTGAGCCACCG[C/T]GCCTGGCCAAAATAT | 9873 |
rs539342205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987354 | TTTCTAGGCTTTCCT[A/G]AAAGTGTTTTCACAT | 9873 |
rs539351744 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071100 | TACTAAAAGATGGTC[C/T]ACCAATTATTTTACA | 9873 |
rs539360588 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065020 | CATGAGGCCAGCATC[A/G]TCCTGATACCAAAGC | 9873 |
rs539362833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038122 | GACGAGGTGGGAAGA[C/T]TGCTTGAGGCCAGGA | 9873 |
rs539372352 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940960 | TGGATCACCAAAGCA[A/C/G]TCTATAAGCACAGGG | 9873 |
rs539375031 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079259 | TGGAGTGTGGTGGCC[A/T]GATCTTGGCTCCCTG | 9873 |
rs539380841 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979128 | CTCCCAAGGTGCTGG[A/G]ATTATGGGTGTAAGT | 9873 |
rs539386184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915732 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 9873 |
rs539386411 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888457 | GGAGGTGAGATTCTA[C/T]AGATAATAAGCATAG | 9873 |
rs539400449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961536 | GCTATGATTACAGGC[A/G]TGAGCCACCATACCT | 9873 |
rs539409174 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922218 | TTAGAGACAAAATGC[G/T]TGGGTTCTGATCTTT | 9873 |
rs539412430 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017323 | TGGTCCCCTAACACT[A/G]TAACAGGGCCTAATG | 9873 |
rs539422421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909451 | CAGCCTCTGCCCAGC[C/T]GCCACCCCATCTAGG | 9873 |
rs539433107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013832 | AAATAAACTTGGAAT[A/G]TAACTCCTGGCCTCA | 9873 |
rs539447303 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999900 | ACAAACACACACACA[C/T]ACACACTTTCTTCCA | 9873 |
rs539462885 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050580 | AGGAACCCAGGCCCC[C/T]ACAATGGTTTTTCAG | 9873 |
rs539466911 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980061 | TTTAGACAGGAACAA[C/G]TGCTACTGAGACTCT | 9873 |
rs539467502 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018372 | GTCTTTTTCTAAAAC[A/G]CCTTTTCTAATCACT | 9873 |
rs539470227 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962016 | AAGCATTGTTATTGA[A/C]ACCTAAGAATTCCAT | 9873 |
rs539474210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880786 | GTGGGAGGATCACCT[C/G]AGCCTGGGGAGGCCA | 9873 |
rs539491704 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989672 | TACACATATACATTC[A/G]AGGAGAAGGGATGGA | 9873 |
rs539496497 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855320 | AACAAACAAAAAAGA[A/C]CAAAAAGTTGCTGGG | 9873 |
rs539509495 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873344 | AAAAAAAAAAAAAAA[C/T]GAATCTTTTCATGTG | 9873 |
rs539528816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081924 | AAAAGCATTCAAGAT[C/T]GGGCGCGGTGACTCA | 9873 |
rs539530614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903012 | TCCCAGCTCTAAAAT[C/T]GTATGGGCCTCTTAA | 9873 |
rs539532537 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010531 | CTTCCAGTTTTTTGA[A/T]TTTGCTTCTGTAGGG | 9873 |
rs539533057 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994759 | TGACAGAGCGAGACT[C/G]CATCTCAAAAAACAA | 9873 |
rs539560771 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027796 | TGCAGCCTTGGGACA[C/T]GGTGCCCTGCACCCC | 9873 |
rs539567932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894959 | AATCTGGAAAATTCT[G/T]AATTTTGACATGTAT | 9873 |
rs539593531 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991959 | TCAATTAGGAAAAGA[G/T]GAAGTCAAATTGTCC | 9873 |
rs539613510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011470 | AGTGTTAACCCACAG[C/T]TTGGCCCCAAGGGCA | 9873 |
rs539614568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903685 | CTACCATATCGCTTA[A/C]CCCTTACTTGTCTTT | 9873 |
rs539616130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020182 | TTGTTTTACCTCTCA[A/G]TAACACTTGCTGTAT | 9873 |
rs539623543 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099326 | CCAGGATGTGAAGAA[A/C]TTAGAACCCTCATGC | 9873 |
rs539625488 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144248 | AGGCCAGGCGCGGTG[C/G]CTCACGCCTGTAATC | 9873 |
rs539636312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141282 | CTCGCCCCTCAGCCG[C/G]GGACGAGGCAGGACC | 9873 |
rs539638875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994753 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTCAAA | 9873 |
rs539648781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911416 | GAAGTCACACAATAT[C/G]ATTCCTTGAGTTCTT | 9873 |
rs539652286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940463 | AAATAAGCTATTTTC[C/T]TTTCTGTCTGGCAGT | 9873 |
rs539709326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115134 | CCCTCTGACTATGGC[G/T]GGCCTAAATGCTCCC | 9873 |
rs539718449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887740 | TATAGACTTACTAGT[A/C]ACAAACTTACTACAG | 9873 |
rs539723035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857638 | TTTTTTAGTAGAGAC[A/G]GGGGTTTCACTATGT | 9873 |
rs539732032 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967863 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 9873 |
rs539748684 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133353 | AATAATAGTAAAAAG[G/T]AGAAACAACCCATAT | 9873 |
rs539749155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114258 | CTACTGCCAATGTTC[A/C]CTTCAGGCTCAAGTG | 9873 |
rs539757430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880055 | GCTACCCAAACCAAA[C/T]CAAAACAAGACAAAA | 9873 |
rs539766303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041354 | CCTACCAACAATGTA[C/T]AAGAGTTACCTTTTA | 9873 |
rs539771295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897432 | TAGCATAGCATTTAC[A/T]TTGTATTAGGGATTA | 9873 |
rs539772183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121816 | AACATGGATTGCTGG[A/G]CTCCACTCTCAGAGT | 9873 |
rs539773691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088796 | TTCACCATTTAAAAA[A/C]CTCTAAAAAGCCTAT | 9873 |
rs539782166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850264 | GAGATGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 9873 |
rs539792834 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004342 | ATAGCACCTCCATGG[C/T]CATAACCTAGATTCT | 9873 |
rs539792940 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966225 | AGTGCAGTGGTGCGA[C/T]GTCGGCTCACTGCAA | 9873 |
rs539796980 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925037 | TGAGTTCAGCAAATG[A/G]TAATACAGGCATCAT | 9873 |
rs539823846 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838513 | CATATAAAAACAGAC[C/T]ACTGTTAGGCATGAG | 9873 |
rs539825660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021530 | CATGAACACATAGAG[A/G]AGAACAACAGACACT | 9873 |
rs539830431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034276 | ATATATTTACAGATA[C/T]GTTAAAGTGGAATTT | 9873 |
rs539870164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027464 | CTTTTTCTGAAAGCA[C/T]ACAGTCATATCCAGT | 9873 |
rs539870271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867437 | AGTCACCTTCAGACT[A/T]AGCCCACGTACTAAG | 9873 |
rs539883238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925692 | GTAGACACGATTATC[A/G]AAATGGCTGCCAAAG | 9873 |
rs539888308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022438 | AATACAACGTCAATA[C/T]TCCAAAGTTAATTGC | 9873 |
rs539904169 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957247 | GTCCATGTGATCTCA[C/T]TGTTCAATTCCCACC | 9873 |
rs539918488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906473 | TGTTGCCATTGCTTT[C/T]GGTGTTTTAGTCATG | 9873 |
rs539918962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917024 | GAGTGTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 9873 |
rs539926652 | in-del | -/TTAA | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130696 | TGTGACAAAAAAAGT[-/TTAA]TTAAACAGACCCTCT | 9873 |
rs539930198 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019478 | TTATGAAATTAATTT[G/T]TTAACTTTGTGCATT | 9873 |
rs539938822 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025687 | TTTAAAAATTTTTTA[A/T]ATCTCCTTGGAATTA | 9873 |
rs539944349 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014843 | ACCTCAAAAAAGAAA[A/C/T]CAAATTCTTTTTTTT | 9873 |
rs539955833 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937143 | ATAGCTGGAGGAAGA[C/T]AGAGCTAGAGGACCA | 9873 |
rs539955932 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143599 | TGCCCAGGGAGGTTT[G/T]TTTTTTTTTTTTGAG | 9873 |
rs539974737 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081213 | GGCCGAGGCAGGTGG[A/C]TCACAAGGTCAAGAG | 9873 |
rs539976455 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131506 | TGCACTCCAGCCTGG[A/G]TGACAGAGTGAGACT | 9873 |
rs539991232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910392 | TCGAAAAGAAAAGGG[A/G]GAAATGTGGGGAAAA | 9873 |
rs539993940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059803 | CTCATCCCAAGACAA[C/T]GAAAACCCACGGTTA | 9873 |
rs540005083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135965 | CCCAGGAGTTCAAGA[C/T]GAGCCTGGGCAACAA | 9873 |
rs540007823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917623 | GAGTGCAGTGGCTGA[C/T]GCCTGTAATCCCAGC | 9873 |
rs540007880 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857407 | TACTAACGTTTACCC[C/T]TTCTTAGATGTTGTA | 9873 |
rs540020710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006311 | CCTTTACACCTAACA[C/T]GTACAAAACTAAATT | 9873 |
rs540024386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955278 | GGAAACATTTTATTT[A/G]TACTTACTCATTTAT | 9873 |
rs540027946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904888 | GGGAAGAAATGACAA[A/T]CATGTAATTTTTATT | 9873 |
rs540061134 | in-del | -/AAAAAAAAAAAAAAAAAA | 0.381308 | 0.21274 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126340 | GCAAGATTCCATCTT[-/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAATT | 9873 |
rs540062237 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143272 | AGGACTAGAATCTGC[G/T]TCAGGAAGTGTTCTA | 9873 |
rs540071635 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854183 | CATGTTTCTTCAATA[A/C]ATTAAACACAGAATT | 9873 |
rs540083734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998544 | AGACTCTGTCTCAAA[A/G]AAAAAAAGTTAATTT | 9873 |
rs540084868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899672 | AGCCCAGGAGGTTGA[A/G]GCGCAGTGAGCCGTG | 9873 |
rs540092774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057783 | CAAACAATGTATTGC[A/G]CCCCACAGCTATACA | 9873 |
rs540116730 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132649 | ACAACATGGCAAAAC[C/T]CCATCTCTACAAAAA | 9873 |
rs540121267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900454 | GATTTAGGGCTGCAG[C/T]TGGGCTGGGAAAAAG | 9873 |
rs540124388 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105404 | ATAAGACACCACCAT[A/G]CCCCAGAATCTACCA | 9873 |
rs540126967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943768 | AATAAGATACATAAA[C/T]ATTGTATTTTGATAT | 9873 |
rs540141432 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890903 | ATTAGGAATTTTTTT[A/T]AAAATATAAATTACC | 9873 |
rs540148569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949082 | TAAAGTATACAATGC[A/G]GTGGCTTTTAGTATA | 9873 |
rs540159314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049136 | ATGTAAAAAGACGTA[A/G]TGGTTTTTGAGTTTG | 9873 |
rs540167154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936800 | TCAAAGATGATATTC[C/T]TTATTTGCTGAGATA | 9873 |
rs540169878 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054706 | TTCAGACAGAGTCTT[A/G]GCTTTGTCACCCAGG | 9873 |
rs540171881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044619 | TTCTATTAATCTACA[A/G]TAATAGAATTCAAAC | 9873 |
rs540176923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084054 | GGATATTATAAAATT[C/T]AGTTACTTGAAATAC | 9873 |
rs540181666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101166 | CCTGAGGTTTAGTTC[C/T]GACCTGAAGGAGAAA | 9873 |
rs540192638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074212 | TGGAGTGCAGTCAGG[A/G]GGAATAAACTTTTCA | 9873 |
rs540197933 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888987 | ATTGAGACAGAGTCT[C/T]GCTGTCGCCCAGGTT | 9873 |
rs540210590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029367 | TGCAATTATTTTAGA[A/C]TTCTAGAAGCCACTG | 9873 |
rs540211056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061301 | TGTCGCATGGTTTTC[A/G]CAAACTGCAGACCAG | 9873 |
rs540227605 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955920 | CCCACTACGGACTCA[A/C]AGTAATAGCACACAG | 9873 |
rs540233680 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928537 | GATGGTTAACACAGG[A/C]AACTGACATTTACTA | 9873 |
rs540236258 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861357 | CCTTAATAACCCTGT[A/G]TCTACTAAAGAAATG | 9873 |
rs540244274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974074 | GACAGGTAAGGGCGG[A/G]GGGCGGGATGGAAGA | 9873 |
rs540251415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066313 | CAGAAAATTGAAACC[A/G]GATCCCTTCCTTACA | 9873 |
rs540251468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075010 | CTTTAACAGGCACTT[A/C]ATAACACAAAATATT | 9873 |
rs540260318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929921 | TAATAAATGATTATT[A/G]AAATGAATCAAACTG | 9873 |
rs540266730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920262 | GGCACACACAATATT[A/T]AAAACAAAAACAGAG | 9873 |
rs540270234 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095146 | GTGTTCTTATTTCTT[A/T]TTAATTAGGTGACCT | 9873 |
rs540279475 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966157 | TTTATTATTCTTCTT[G/T]GAACTGAGCCTTTTT | 9873 |
rs540293011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957601 | AGAAATAAAAAAGAT[A/G]TTTTTGGAACATCTC | 9873 |
rs540294849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966456 | TGAACCACCACACCC[A/G]GACTAAACTGAGCAT | 9873 |
rs540294924 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924287 | AGCTATTTTTCTTTC[-/T]TTTTTTTTGAGACAG | 9873 |
rs540303537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913393 | CACACCTCAGCCTCC[C/T]GAGCAGCTGGGATTT | 9873 |
rs540331289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030669 | ACCAACAAAGAAAAA[C/T]ATATTAATAGTACTG | 9873 |
rs540331771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851507 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 9873 |
rs540345138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921521 | CCCATGTGAGCAGAG[A/T]GCATTTAAACTCTGA | 9873 |
rs540348279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930563 | CAGCCTCACCAACAA[C/G]GTGAAACCCCGTCTC | 9873 |
rs540350042 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014611 | AATCATCTGATGTCA[A/G]TCATCACTGACAATT | 9873 |
rs540377480 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038347 | CCCTGTCTCTTTAAG[-/A]AAAAAAAAAAAAAAA | 9873 |
rs540382562 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076978 | AGCCAGGCATGGTGG[C/T]GGGCACCTGTAGTCC | 9873 |
rs540382645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922585 | TTGAGGAATGATTAA[A/G]CTATGATGTGTACTG | 9873 |
rs540389848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852031 | ATAGGTGTGCACCAC[C/T]ACACCTGGCTAATTT | 9873 |
rs540394990 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131255 | GGGCGCAGTGGTTCA[C/T]GCCTGTAATCCCAGC | 9873 |
rs540406396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967390 | AATGGGTAAACAAAA[C/T]ATGGTATATCCATAT | 9873 |
rs540423917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060513 | AGAAAGTTTTCCAGG[C/G]GAAATAATCAATAGT | 9873 |
rs540427139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914089 | GCATAATCTCAGCTC[A/G]CTGCAAACTGCGCTT | 9873 |
rs540436049 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863493 | TCCATAAAAGAAAAA[C/T]TGGTAGGTTGGACTT | 9873 |
rs540445327 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068595 | TGGTTTAAAGTTTTA[A/T]CAGTTTTTATACAGT | 9873 |
rs540456984 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105559 | AGTATCTTTACTACT[A/C]TAAGCCTCAATTTTT | 9873 |
rs540463608 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997553 | AGTAATTCAGATAGT[A/G]AAATTATATAATAGA | 9873 |
rs540472315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099595 | AATGTGGTATATACA[C/T]ACAACCGAGTATTAT | 9873 |
rs540495878 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897226 | ATCCTATTTAATTTT[C/T]AAACAAATAAGGTAT | 9873 |
rs540496251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861007 | ACAAATTAGAAAGGA[G/T]AAAATTAAATCCAAA | 9873 |
rs540498193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994849 | TTAAAAAATTGACAT[A/G]TAATTCACATACAAC | 9873 |
rs540504509 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73141993 | TGTGTGAAAGGAGCG[C/T]TTAAGAAGCAAGACT | 9873 |
rs540505708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069769 | TTCTTTCCAGAATTG[A/G]AGAAAAGCAAGAGAC | 9873 |
rs540525093 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033779 | GCTGTGAATTAGTTA[C/T]GAGTATTCTTGGATA | 9873 |
rs540533792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099980 | ATGTGCCGTTTGTCA[C/T]AGAAGCACTCACAGC | 9873 |
rs540534412 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922957 | CTCCATCCCTTCCTT[-/C]CCCCCAGCCCCTGGC | 9873 |
rs540569057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960803 | TGTGAAATACACTCT[C/G]ATAATAAGAATACAG | 9873 |
rs540570583 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837146 | ATCTTAAAAAAACCA[C/G]CCTTTTAATTTCTTT | 9873 |
rs540570757 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931085 | ACCTACTATATACCC[A/T]CAATAATTAAATTTT | 9873 |
rs540571959 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854865 | GAAATGGGCCAGGCA[C/T]GGTGGCTCATGCCTG | 9873 |
rs540576660 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845302 | GGCACGTGCCTGTAA[G/T]CCCAGCTACTTGGGA | 9873 |
rs540581669 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108792 | TAGCCAGGATGGTCT[C/G]GATCTCCTGACCTCA | 9873 |
rs540584639 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837968 | AGAAGAGTATATGCT[C/G]TAAAAATTAAGATGA | 9873 |
rs540592595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891941 | AAATTACTTGAAACA[A/C]AAATTTTCTTATTAC | 9873 |
rs540609142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112087 | TATTACCAGTGAGTT[C/T]TGTACCTTTAGATAA | 9873 |
rs540612343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053803 | GATTCTCTATATTAA[C/T]AGAAGATATCTTCAA | 9873 |
rs540619866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940555 | TAGTCTCATGTCATG[A/C]GCTTTCTTCTGAGAG | 9873 |
rs540629081 | in-del | -/ATAAA | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870554 | ATAATAATTTTTAAT[-/ATAAA]AGAACTTCTCTCTAA | 9873 |
rs540637100 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083361 | CGAGACCATCCCGGC[A/C]AACATGGTGAAACCC | 9873 |
rs540657686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933160 | TAGGCAGATATGCAA[C/G]ACAGAACCTCAAACC | 9873 |
rs540659261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093506 | AGAGCTGTCTTAGAA[A/G]AGCTGTAATGCACCC | 9873 |
rs540663119 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027285 | GAGAAGAGGAACTTA[C/T]TGAGAACTAGAGCAA | 9873 |
rs540672682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119177 | CATAGTGGCACATGC[C/T]TGTAGTCCCAGCTAC | 9873 |
rs540681526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888112 | ATGAGGGTAAAGAAT[A/G]AGAAAACAAGATAGC | 9873 |
rs540699963 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096843 | AAACAAAAAAAAAAA[A/C]GGAAATTTCCTTCCA | 9873 |
rs540719439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116326 | TTTTTACTTATGCTC[C/T]TAAGGCAGACTGGCA | 9873 |
rs540723895 | in-del | -/A | 0.39214 | 0.205661 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985358 | ATATCCAGAATGACC[-/A]AAAAAAAAAAAAAAA | 9873 |
rs540728577 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877080 | GGCTGCCTCCAGTGC[A/T]GCCTCATCCTCCTAC | 9873 |
rs540732231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933682 | ATAATAATTCAATTG[C/T]TTTCCTTACTATTCC | 9873 |
rs540743343 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031200 | TAGAGAATAAAGGCC[A/G]GGCACGGTGGCTCAC | 9873 |
rs540744643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869287 | TCCCTCAAATTAATT[A/C]AGTTCTTCCTAATCG | 9873 |
rs540755433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976462 | TTTTAAATTTTTTTG[C/T]AGAGACAAAGTCTCA | 9873 |
rs540761391 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010096 | TTGTTAATTCTTTCT[C/T]ATTTTTCTTCTTTTT | 9873 |
rs540801960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134457 | CTTGGGTGACAGGGC[A/G]AGACCCTGTCTCAAA | 9873 |
rs540806789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024048 | TGGTGAACTAATATA[C/T]ATAGTATTGTAGTAG | 9873 |
rs540817431 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134923 | TATCTCAGCTCACTG[C/T]AACCTCCACCTCCCA | 9873 |
rs540821692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926386 | GAGAGGATGGCATGA[A/C]CAGTTGCAGAGAGGA | 9873 |
rs540830015 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914476 | AGAGGCATCACGCTA[C/T]CCAACTTCAAACTAT | 9873 |
rs540840504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072260 | TAATGGGGATCAGCA[C/T]CAACAATGATTTCCT | 9873 |
rs540875362 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016289 | GCCTGGGTGACAGAG[G/T]GAGGCTCTGTCTCAA | 9873 |
rs540884388 | in-del | -/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100339 | TTACATGCTTTTGTT[-/G]GTTGTTGTTGTTGTT | 9873 |
rs540889168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963906 | ACCCTGGATTAGATG[A/G]CAACTCTGTGTCATG | 9873 |
rs540891469 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954710 | TGGTCAGGAGATGAG[C/T]AGTGTACAAAGAGAT | 9873 |
rs540918860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141430 | CCCGCAAATTTGCAA[A/G]CGGGCGGGGCTGGCG | 9873 |
rs540921205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854111 | TGGAAAAATTGGAAC[C/T]TTTATACACTGCTGG | 9873 |
rs540928209 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894726 | ATGCTCTGAAAAAGA[A/G]TAAGTATTTTTTGGT | 9873 |
rs540936769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016904 | TTTGAATTGAGAAGA[A/C]CATTTTGTTAAGAAT | 9873 |
rs540937053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008427 | GGTGTTTTAATAAAT[G/T]TTCATACATGGTTGT | 9873 |
rs540958348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865326 | AATATAGGTCCTCAT[C/T]AAGCTATTTTGTGCC | 9873 |
rs540971360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955556 | GCTAAAAGTTCCAAC[C/T]CTTTAATCATGTTTG | 9873 |
rs540986237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096480 | CACCTGAACACAGGA[A/G]GCAGAGGTTGCAGTG | 9873 |
rs540995727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849949 | AAATGGTTGAAAGCC[A/G]GAAAAACACTTAAAA | 9873 |
rs540997249 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989234 | TCAGTGTCCTTCAAA[C/T]TGCAGATTAAAATCC | 9873 |
rs541051900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088516 | GAAAGTTTTCTCTGG[A/G]TCATGGTATTATAGG | 9873 |
rs541097494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004167 | ACGGTACTTTGCCAT[C/T]CTACATATCACATGG | 9873 |
rs541107949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850446 | TAGTGGCGTGATCTC[A/G]GCTCACTGCAAGCTC | 9873 |
rs541125018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988211 | CAGTCAGCACACTGA[A/C]CCTGAGTCTCAGCTC | 9873 |
rs541127576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925373 | AAATCCTACTTTAAA[A/T]ATTCCAGCTGGGTAC | 9873 |
rs541128610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106341 | AGCCCATGAAGTCAA[A/G]GCTGCAGTGAGCTGT | 9873 |
rs541130524 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097999 | ATCTAAGGTTTGCCA[A/G]TAAGTTATCTTTTCA | 9873 |
rs541145153 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054472 | TAGTCTCTGTCTCTT[A/G]GTATCCTAAAATTCC | 9873 |
rs541158516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997176 | GCCGAGAGGCCAAAG[A/G]GTGAGCAGAGATCAG | 9873 |
rs541169568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843023 | AGGACAAACGTGACC[A/G]TATAAAGAAAAGCAT | 9873 |
rs541180653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128779 | TGGTGAAAGATTCTG[C/T]AGCATCACTGGAGCA | 9873 |
rs541197477 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989327 | CCTAACAACCATACA[C/T]TGAGAAATAACCCGA | 9873 |
rs541216278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916615 | CCACTGTGCCCAGCC[C/T]CCTTTGTTCACTTTT | 9873 |
rs541233996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990062 | GTGTTAAGAAAGGAC[C/T]ACAGGGGATGAGACA | 9873 |
rs541235869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882014 | GCTGGGTGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 9873 |
rs541249477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873521 | AAATATTTTCCCCCA[C/T]TCTGTGGGCTGTCTT | 9873 |
rs541251360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842029 | CGCAAACAAGATCGG[C/T]AAACACGTTCCTTCT | 9873 |
rs541258861 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138637 | TTTTTGAGACAGGGT[C/T]TCACTCTGTTGCCCA | 9873 |
rs541288968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879873 | GCTCAGTGGCTCATG[A/C]CTGTAATCCCAGCTA | 9873 |
rs541296056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064641 | AGTGGTGATATCCTT[A/G]TATCAGTGGTGATAT | 9873 |
rs541297165 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122752 | AAAAGTCTCTATTGG[A/C]CTCTGTGAAATTCAT | 9873 |
rs541313673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121171 | CTCTTATACACATAC[A/T]CATACACACACACAC | 9873 |
rs541323444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874783 | TAGGATTTCAGTTGC[G/T]TATAAGTTAAAAATT | 9873 |
rs541338210 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966638 | AATACATTCAACAGA[C/T]ATATATGTCAGTTAC | 9873 |
rs541339746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129579 | ACCCCAGATGGGACC[A/G]TCCAGTTGCAGAAAA | 9873 |
rs541347220 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910363 | AACGGGCCATGATGA[C/T]GATGGCGGTTTTGTC | 9873 |
rs541358903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910634 | AAGGCAGCATGCTCG[C/T]TAAGAGTCATCACCA | 9873 |
rs541363687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026493 | TGCAATAAAATTTAT[C/T]TTAAAATAAAAGAAA | 9873 |
rs541382416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857862 | CTCAGCTTCATGGCA[C/T]AATCATGAGGTAGAA | 9873 |
rs541384549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003300 | ACTTACCTCACAGGG[C/T]TATTTTAAAAATTAA | 9873 |
rs541384964 | in-del | -/A | 0.390277 | 0.206936 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880000 | GTGAAATTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 9873 |
rs541393169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973293 | AATCACTTGAACCCA[A/G]GAGGCAGAGGTTGTG | 9873 |
rs541395657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905191 | GGTAATTATTGTCGG[C/G]TTGTAGTTGGCCACC | 9873 |
rs541397006 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948383 | TGAATGTTTCATTTT[G/T]CAACATTTTAGTTGC | 9873 |
rs541403855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012910 | AAATATCTCTGAAAT[C/G]TTCCCTACAACTTGA | 9873 |
rs541404256 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108266 | TATTAGATCTTTTCC[C/T]ATGAAGTTGTTTAAG | 9873 |
rs541428078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007470 | TACAAAAAAAATTTT[A/T]AAATTAGCCAAGCAT | 9873 |
rs541431846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861747 | CCAACCTGACCGACA[C/T]AGAGAAACCCTATCT | 9873 |
rs541438935 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944563 | AGGGCAATCAGGCAG[C/G]AGAAGGAAATAAAGA | 9873 |
rs541444357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951822 | TTCTTAATATCTAAC[C/T]GAGATCAATCATGCT | 9873 |
rs541464083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896987 | GCCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 9873 |
rs541465767 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108742 | CCCGGCTAATTTTTT[G/T]TTGTATTTTTAGTAG | 9873 |
rs541483596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905659 | TGTTCTCATTGTTCA[A/G]CTCCCATCTATGAGT | 9873 |
rs541503976 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981672 | TGAAGCACTATGTAA[C/T]ACCTAATACGATACT | 9873 |
rs541505432 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900664 | AAGTCATTGGCAAAA[C/G]CTGATTTGATTAAAA | 9873 |
rs541508594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845740 | TATAGGTGTTCTTCC[A/G]TCCATCAGGCTCTGT | 9873 |
rs541509569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122467 | CAAAGGTAACACCAC[C/T]TAACCATCTTCTTTC | 9873 |
rs541512046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049379 | TGACAAGAAACAAGA[C/T]AGGTAAAAGGTTTAA | 9873 |
rs541513023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000073 | TAACATTTTACATAA[A/G]GACACATATACATCT | 9873 |
rs541519758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917014 | TTTTGAAGCAGAGTG[C/T]TGCTCTGTCGCCCAG | 9873 |
rs541529150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109302 | GCATTGAATCTGTAG[A/G]TTGCTATAGAAACTA | 9873 |
rs541538838 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850205 | ATAGCTGGGATTACA[A/G]GCACCCACCACCACA | 9873 |
rs541539263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115384 | GAGATGGGGTTTCAC[C/T]GTGTTAGCTAGGATA | 9873 |
rs541540547 | in-del | -/A | 0.499424 | 0.0169631 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039517 | AGAGACTCCGTCTCC[-/A]AAAAAAAAAAAGAAA | 9873 |
rs541563560 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050712 | TTAAAGTCCCTTTAT[A/G]TTGGTTGAACGTTAT | 9873 |
rs541568066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997761 | GCTGGAGTGCAGTGG[C/T]ACGATCTCGACTTCC | 9873 |
rs541571275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130172 | AGCCACCGCGCCTGG[A/C]CCATAATCTCTTATA | 9873 |
rs541571862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846331 | GATTACAGGTGCACA[A/C]CACCATGCCTGGCTA | 9873 |
rs541575554 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042239 | TGAGATTATTTTTAA[A/T]CTCTGGTGAAAGACA | 9873 |
rs541576359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992505 | CTACCTGACTTCAAA[A/C]TATACTACAAGGCTA | 9873 |
rs541576845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090477 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 9873 |
rs541609609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035239 | GCTCTGTCACCCAGG[A/T]TGGAGCGCAGTGGCG | 9873 |
rs541612099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000826 | GCAGTTAATAAAACA[C/T]AGTACTTAATGAGAA | 9873 |
rs541616682 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088103 | GTCCTGAACTCCTGG[C/G]CTCAAGCAATCCTTC | 9873 |
rs541618649 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060775 | TGAAGTTAGAAATAC[A/G]CAAAACTCTAGGTTA | 9873 |
rs541625697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889772 | AAAACTCAGTTCCTT[A/C]AACTGTTTGACATTT | 9873 |
rs541628263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093742 | AAGTAGCTGGGATTA[C/T]AGGCATGCACCACCA | 9873 |
rs541637150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945755 | TGAACAGACACTTCT[C/T]AAAAGAAGACATTTA | 9873 |
rs541642565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042894 | CTACTGATTTTTGTA[C/T]GGTGATTTTGTATCC | 9873 |
rs541662887 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090030 | GTAATCAGGAATATA[C/T]CTAAATATATCTACA | 9873 |
rs541666894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893931 | GCTCTCTCAAGATAT[C/G]ATTTTGTTTTATTTT | 9873 |
rs541672478 | in-del | -/TATG | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883055 | AAGGTAATGGGAAAA[-/TATG]GCATACTCTTTAAAA | 9873 |
rs541676121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927403 | GGGGTGATGATGATG[C/G]TGTCAGTGTAGGTTC | 9873 |
rs541686542 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085586 | ACCACATTTAAGGGA[A/G]AAATTGAAAAGTCAC | 9873 |
rs541715991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886094 | CTGGAGTTCTAAGGG[A/G]GTGTTAGAAAACCAT | 9873 |
rs541728684 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883192 | TAGAAATGTTTAGGA[C/T]CACAGTCCACAAAGA | 9873 |
rs541749339 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909234 | TGGAGACGGGGTTTC[A/G]CCCTGTTGACCGGGC | 9873 |
rs541755217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878698 | AGATAAAAATCTATA[A/G]TAAGTTGAAATGATG | 9873 |
rs541764264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927964 | TTTACTTACTTTATC[A/T]TGTTAATGATTTTCT | 9873 |
rs541792498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123400 | GTAACTCCTGGAAAA[A/G]TAGCGCTCATCCTTA | 9873 |
rs541803180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908217 | TGACAGGATCTCATT[C/G]TTTTTCATGGCTGAA | 9873 |
rs541813622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087447 | TGTGGTGGCTCACCC[C/T]GTAATCCCAGCATTT | 9873 |
rs541834112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032926 | GCTTGCGAGCAGTGC[A/G]GTGCCATTATCAGAC | 9873 |
rs541835306 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008392 | GAATAATTTATATAA[A/T]AACTAGTAACAAGAA | 9873 |
rs541862051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952481 | AGGCATGTGTCACCA[C/T]GCCCAGCTAATTTTT | 9873 |
rs541873159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070102 | GAAACTTATCAGTAA[C/G]AAGAATTTCATTGTC | 9873 |
rs541890553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901278 | GGTGCGTGCCTGTGG[C/T]CCCAGCTAATCGGGA | 9873 |
rs541892771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131014 | AATTGAGAAGCAACT[A/G]TGATTGTTGAATGAA | 9873 |
rs541896944 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908789 | CTCCCATCTCAGCCT[A/C]CTACAGACATATGCC | 9873 |
rs541915920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871390 | TGTCATTCTCTTTTG[C/T]TTAGCAAGTAAAACA | 9873 |
rs541926175 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949207 | TAATCCCAGCACTTT[A/G]GGAGGCCCATGGCGG | 9873 |
rs541949784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945274 | TCTGATCTTTGACAA[A/C]CCTGACAAAAACAAG | 9873 |
rs541960262 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060388 | GACATTTTGTATAAT[C/T]TCATTTCAAACATTC | 9873 |
rs541963001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863429 | GGAGAAAATCTTTAT[C/G]ACCTTGGTTTTAGGC | 9873 |
rs541970878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045081 | TCTCAAAAAAAAAAA[A/G]AAAGAATGGGGTAAA | 9873 |
rs541979431 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915946 | CTGGAGGCCACTATC[C/G]TTAGCAAACTAATGT | 9873 |
rs541981055 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028102 | CACACAGAATGCTCA[C/G]AGGGGCACTGCCTAC | 9873 |
rs541985238 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984854 | GAAACTTATCCCTAA[C/T]GCAGTCTTGAGAAGC | 9873 |
rs542019926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137886 | CAGCTGGGTTGCAGA[A/G]AACCATATATACTAT | 9873 |
rs542025111 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894188 | GCCAATGGCATAACA[A/T]TCTAGTTAACCCTCA | 9873 |
rs542025743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938076 | CCAGGTAGGGAAATA[C/T]ATCCCCAGCACCCTC | 9873 |
rs542034053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045662 | TCTCAGTAAACTATC[A/G]CAAGAACAAAAAACC | 9873 |
rs542039410 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094519 | CCAGTTGTCCATCAA[C/T]GGGATCATGGATAAA | 9873 |
rs542040866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120352 | AACAATGTACATTTT[A/G]AAAGTCTATTAAGTA | 9873 |
rs542063523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903308 | TGCAAGCTCCGCCTC[C/G]CGGGTTCATGCCATT | 9873 |
rs542073071 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131419 | CTGTAGTCCCACCTA[C/T]TCAGGAGGCTGAGGC | 9873 |
rs542074305 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963641 | GGTAGGGTGGGGTGG[-/T]TTTGGGATGAAACTG | 9873 |
rs542087817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010650 | CGATTTCTTTGGCTA[G/T]GAACAGTGTCAGTGG | 9873 |
rs542098553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903971 | GGGGGATATATAGAT[A/G]AATAAGACAAACAAA | 9873 |
rs542101962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128928 | CCAGGCTGGAGTGTA[C/G]TGGTGTGATCTCAGC | 9873 |
rs542105093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985977 | ATGTGTTGGCAGCTG[C/T]GCCTCATGAAGTAAA | 9873 |
rs542113645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930729 | GCCTGGGTGACAGGG[C/T]GAGACTCTGTCTCAA | 9873 |
rs542120337 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091238 | TCATGTATAAATCTG[C/T]ATGTAAAGACACGTT | 9873 |
rs542120558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056318 | ATCTTTAAAATCTCT[C/T]TGATGCAAACAAATT | 9873 |
rs542123212 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032215 | TTTTTATTCTTTATA[A/C]CACTGGATTGTTCAA | 9873 |
rs542124989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939984 | GAACATCTGTGGACT[A/G]CTTGTACAGTCCCCT | 9873 |
rs542125004 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136166 | CTCTTGTCTCTTAAG[A/G]AAAAAAAAAAAAGAA | 9873 |
rs542141853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977617 | TAGTATATGTGCTGC[C/T]GAAGCGAGCACGCTC | 9873 |
rs542153249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047526 | AAAATACTGGTCATT[C/G]ACAGTACCTAGCCAC | 9873 |
rs542159670 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126255 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 9873 |
rs542167738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947200 | GTTAAGGGCTTTAAA[C/T]CAAGTGGAAGACCTA | 9873 |
rs542186952 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961082 | CCTAATGCTTTCCAT[C/G]GCCAACATTGTGACT | 9873 |
rs542192116 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047687 | AGAACCCCCTTCTCT[G/T]TTCCTTTCATTTGGC | 9873 |
rs542194969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123452 | CTATGGCTTTTTATA[C/T]ATGCGCAGGCCTCTC | 9873 |
rs542201239 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923822 | CGTCTGCCTGTAATC[C/G]CAGCTACTTGGCAGG | 9873 |
rs542241603 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095075 | TCATTTGAATACAGT[A/G]TAAACAGATGATGCC | 9873 |
rs542250198 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910893 | TATATTCTCATTATT[A/G]ATCCTCTGTCAGATG | 9873 |
rs542255702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927323 | GTGGATACATATCAT[C/T]ATACATTTGTCTAAA | 9873 |
rs542268497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969062 | TTTTCTTTGAAATCA[A/T]TTTAAAATAGTATAC | 9873 |
rs542272239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875046 | TAACACAACATTTAA[C/T]ATAAACACATATAAG | 9873 |
rs542284297 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950178 | AATCCTTGCCCTTTT[-/A]AAAAAAACTGGGTTA | 9873 |
rs542294380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918167 | GTATTATTGTAGTTG[A/G]AATTATTTTCTTAAC | 9873 |
rs542300319 | snp | C/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841781 | CTTCACTTTTTCCTC[C/T]TACAGATCTCATCAC | 9873 |
rs542301105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114365 | GGGCAGGTCCAGAAA[C/T]GCTGTCCAAGGGCCA | 9873 |
rs542302276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862859 | AAGTCAGTGCAATAC[C/T]GGCATCAAGCTGGAC | 9873 |
rs542303509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961090 | TTTCCATCGCCAACA[C/T]TGTGACTTTTCACCC | 9873 |
rs542321534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070739 | CCTAAATGTCAAATT[A/T]AAAAAAAAAAAGAAA | 9873 |
rs542337339 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975394 | GAGAGGTTGGTTAAT[A/G]GGTATAAAATTACAG | 9873 |
rs542343605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074115 | TTCAAAGATAGGTCA[A/G]TTGACTAGAATAAAA | 9873 |
rs542346268 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854903 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 9873 |
rs542348141 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901645 | CTCACACTTTAACTA[C/T]GGTTAAAAATGGTAA | 9873 |
rs542352851 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905682 | CTATGAGTGAGAACA[A/T]GCAGTGTTTGGTTTT | 9873 |
rs542372671 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945502 | GGGCAAGGACTTCAT[A/G]TCTAAAACACCAAAA | 9873 |
rs542375577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912621 | TGATTTTGGTATCAG[C/G]GTAATGCTGGCCTTA | 9873 |
rs542391002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961957 | TGTATTTGTTTCATC[G/T]CTGCATCCCTGAAAG | 9873 |
rs542392276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954039 | GAAATGACATAATCT[C/G]ACTTAGGTTATAAAA | 9873 |
rs542403930 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022705 | AATCTCAATCAATAG[C/T]CCAGAAAGATAAAGG | 9873 |
rs542409693 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962518 | AGAACAGGAGTTTAC[A/C]AAATATACTTTATAT | 9873 |
rs542426219 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058811 | GACCTCAGGTGATCC[A/G]CCTGCCTCAGCATCC | 9873 |
rs542440304 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057799 | CCCCACAGCTATACA[C/G]GGAATGAGTTCCCCT | 9873 |
rs542463124 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906273 | CCACTTTTTGATGGC[A/G]TTGTTTTTTTCTTGT | 9873 |
rs542474376 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957349 | TCATCCATGTCCCTA[C/T]AAAGGACATGAACTC | 9873 |
rs542480135 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946548 | CTTAAAGTATAATTT[A/T]AAAAAAACTAGACAA | 9873 |
rs542484785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005416 | ACCTATCAGCAACAC[C/T]GACCTAGTTTATCCT | 9873 |
rs542485760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059719 | CTGTGAGGTTTTCTT[C/T]CTTTTTTTTTCTTTT | 9873 |
rs542511208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950260 | CTTTTCAGATATGTA[A/T]TTTGCAAATATTTTC | 9873 |
rs542511976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954662 | GTAGCAAGTTTGGGA[A/G]GGAAAAATCAAAGGC | 9873 |
rs542516914 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127563 | CTGATACCAACAACA[C/T]AGAATGGCATCTGTG | 9873 |
rs542522066 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957933 | CAAGTTTGGAATTAT[A/G]TAAACATAAATTATT | 9873 |
rs542533275 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088541 | TATAGGCTTCCTTTA[C/T]TTTCTTCTTTTGCTT | 9873 |
rs542539915 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898790 | GATGGAATGCAGTGG[G/T]GTGATCACGGCTCAT | 9873 |
rs542542028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104120 | TCATATAGTTGCTGG[C/T]GGCTAACAGTGTAAT | 9873 |
rs542549052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051746 | AAAACAACAAAAAAA[A/T]TTTGAAATAAATAGT | 9873 |
rs542551570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840497 | CTTTAAGGCCATGAA[A/G]TTAGCTTATTATTTC | 9873 |
rs542557136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943157 | CCACCATGCCCAGCT[A/C]ATTTTTTGTATTTTT | 9873 |
rs542567047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124273 | TGTGGGATGGGGGGA[C/T]GGGGAAGGGATAACA | 9873 |
rs542577977 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978998 | GAGTAGCTGGGACTA[C/T]AAGTGCATGCCTCCA | 9873 |
rs542582427 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110235 | ATATTCCCTCCTCCT[C/T]TATTTTTCAGAATAG | 9873 |
rs542584199 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047052 | TGATAAAAAATACTA[C/T]TAAATATAAAAGACA | 9873 |
rs542586783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035886 | CCACCACACCCAGCT[A/T]ATTTTTGTATTTTTA | 9873 |
rs542590498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943640 | TTGACTTTTGAACAT[A/G]TATGTTTCAGTGTTT | 9873 |
rs542593788 | in-del | -/CAG | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080421 | ATTCATATTTACACA[-/CAG]ATACACAGCATAAAT | 9873 |
rs542604257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091337 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 9873 |
rs542609154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981839 | TTAAGAAATTAGCTG[A/G]GTATGGTGGCAGGCA | 9873 |
rs542629670 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119286 | CCAGCCTGCACAACA[A/G]AGCGAGACTCTGCCT | 9873 |
rs542629814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073313 | TTACTTCTGGAGAAT[C/T]ACAAAGTGAACTTCA | 9873 |
rs542647837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139313 | CAAGGGAAATAAGAA[C/T]TGCAGCCACTCTTGC | 9873 |
rs542662466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875370 | TATCTATCTAGCTAG[C/T]TATTATTTATTTGAC | 9873 |
rs542665551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083070 | ATGCGTGATGAAAAA[C/T]TAACCTTTCATAAAC | 9873 |
rs542684931 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871462 | TGTTTCACATATGCA[A/G]GTGGTGATCTCTTCC | 9873 |
rs542693047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065577 | AAATTGTCTCTGTTT[A/G]CAGATGACATGATTG | 9873 |
rs542704750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084420 | TTTAGAGATAGGGTC[G/T]TGTTCTGTTGCCTAG | 9873 |
rs542705938 | in-del | -/TAATT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008380 | TTCATAACCTAAGAA[-/TAATT]TATATAATAACTAGT | 9873 |
rs542707943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036900 | TTCAAAGTTAGTGTT[C/T]CCTACCATCAAAATC | 9873 |
rs542715395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937166 | GAGGACCAAAGGCTT[A/G]ATGAAGGAACTCTTA | 9873 |
rs542715478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867269 | TGGTACTTAGATCTC[C/T]AACATGAAAAACTAA | 9873 |
rs542729908 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919133 | ATAAAATAAAAAAAA[A/T]CTAAAAAGTGTCAAA | 9873 |
rs542735020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964979 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 9873 |
rs542751474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858066 | CCCCTAACACATGTT[C/T]GGTGCATAGGAGGTA | 9873 |
rs542754998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982959 | TGAAGCCAGGAGTTT[C/G]AGGCCAGCCTGGTCA | 9873 |
rs542763315 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928892 | CCCACCCCACAACAG[G/T]CCCCGATGTGTGATG | 9873 |
rs542771652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965432 | TTACATTCTACCAGG[C/T]GAGACAAAATAAGTC | 9873 |
rs542812943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858748 | AACAAACCTGCAATT[A/G]TATCCCTGAACTTAA | 9873 |
rs542814803 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094315 | TGGAACTCTAACATG[A/C]CATTGGTGGGAATGT | 9873 |
rs542827667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075934 | GACCAGCCTGGGCAA[C/T]GTGGCAAAACCTCAT | 9873 |
rs542849202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920644 | ATAGAAGGAACAAAG[A/G]TAAGATTTTTTCATA | 9873 |
rs542853495 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090707 | AGACCTTTTACTACA[C/T]TCCTGTTTGTACTAT | 9873 |
rs542862724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958199 | TCAGAGGAAAACCTT[C/T]GGAGCTAAGGACTAG | 9873 |
rs542874383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966955 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGTG | 9873 |
rs542881940 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851879 | TCAGTCAGAGTGGCT[-/TT]TTTTTTTTTTTTTTG | 9873 |
rs542882012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868240 | ATCCTCAGCAAACTA[A/C]GGCAGGAACAGAAAA | 9873 |
rs542898894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076836 | TTATGCTAGGCCCGG[C/T]GCAGTGCCTCACGCC | 9873 |
rs542927247 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851458 | AAAAATAAAGGTTGC[C/T]GGCCGGGTGAGGTGG | 9873 |
rs542934294 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043118 | GTGAAAGTGGGCATC[C/T]TTGTCTTACTCCACT | 9873 |
rs542940225 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967803 | TTAAAAAGAAGTGGG[A/C/G]AGAGAGGCTGGGTGC | 9873 |
rs542947726 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107053 | TATATATATATATAT[A/T]TTTAAATGGAGTCTC | 9873 |
rs542957383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015668 | AAACATTAAAATTTT[G/T]ATAATTTTGAAATTA | 9873 |
rs542960640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959378 | GGGACTACAGGCGCC[C/T]GCCACCATGCCCGGC | 9873 |
rs542990058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060969 | AGGAACAAGAACTTA[C/T]ATAGAACTGTTGATA | 9873 |
rs542990882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946375 | CATAGGAAGGGGAAC[A/G]TCACACACCAGGGCC | 9873 |
rs542991125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939166 | ATTCTAAAGTCAATT[C/T]CAGCAAAAACTTGTG | 9873 |
rs542997548 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010522 | TAGTCACTTCTTCCA[A/G]TTTTTTGAATTTGCT | 9873 |
rs543008156 | in-del | -/TAAGC | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059028 | TCCCATTTTAGTTTT[-/TAAGC]TAAGCTAAGAAATAC | 9873 |
rs543017989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890726 | ATCATTTTATAGAAA[A/G]GAAAACAGAGGCTCA | 9873 |
rs543024992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993933 | AAATAAATAAATATC[A/G]GATAGAAAAGCCAGG | 9873 |
rs543032403 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836962 | TTAGCAGCTCTTCCA[A/G]AAAATATTTTAAAAT | 9873 |
rs543038619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099894 | CTCCGAGGGGACTTT[C/T]GGCACTTGCCTCTGC | 9873 |
rs543047095 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053971 | TTTATTGTATTTTAC[-/A]AAAATGTCCATCTAC | 9873 |
rs543057831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990863 | TAACTAAGACCAGAA[C/T]AGAACTGAACGAAAT | 9873 |
rs543060962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044508 | CTTGTGCCCAGGAGT[C/T]TGAGGCTGCAGCGAG | 9873 |
rs543078969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939902 | GGATTACAGGCATGA[A/G]CCACCATGCCTGGCC | 9873 |
rs543096840 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043943 | TTGAATCATCATCCC[C/T]TGGAAGGCCATTCAC | 9873 |
rs543099743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092839 | TAACCCTACCCAAAG[A/G]CAGGTCTTACCTTTG | 9873 |
rs543108864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087618 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCGGGA | 9873 |
rs543109739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087691 | GCCTGGGCAACAGAG[C/T]GAGGCTTTGTCTCAA | 9873 |
rs543113931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940505 | AAGCCAAGATGGGTG[A/C]ATACCCGCACATCCA | 9873 |
rs543118927 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991475 | TCAATAAAATACTGG[A/C]AAACCAAATCCAGCA | 9873 |
rs543122281 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037555 | CTCTGGTATAGAATG[A/C]ATTCTTTCTCCATAT | 9873 |
rs543144853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983571 | GATACACTATAAAAA[C/T]ATATTTTTAATAGAA | 9873 |
rs543159156 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040895 | AACTGCTCCCCCCCC[-/T]TCTTTGGTAACTATC | 9873 |
rs543175766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884191 | TTTCTGCCTAAAACA[C/T]TAACCTGCCTCTAAT | 9873 |
rs543176931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978659 | TGATTGTGACTGAGT[C/T]CTCACGATATCTGAT | 9873 |
rs543212968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079425 | GGCTGGTCTCGAACT[C/T]CTGATGTCGTGATCC | 9873 |
rs543215946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969693 | TAATTTAATAAGAAA[A/G]CAAATAAAATGGCTT | 9873 |
rs543219061 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73140963 | ATTAGGAAAGAGAGA[A/C]AGCAGCGGCAGCAGA | 9873 |
rs543220395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030420 | ACTCAATTTACCATA[C/T]ATAAATGTATCCAAG | 9873 |
rs543225958 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988416 | TATAATTCACATATA[G/T]TGAATTCATACAATT | 9873 |
rs543238205 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080316 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 9873 |
rs543239742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921388 | ACAGCATATAGATAG[C/T]AGGGCTTAATTTGAA | 9873 |
rs543255735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979188 | AAGCAGTGTGAAAAC[A/G]AACTAATACAACAGG | 9873 |
rs543268216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880222 | AAAACGAATCCATGT[A/G]CAATTGCTATCAAAA | 9873 |
rs543282827 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985549 | AAACTTTCAGGGCTG[C/T]GTGTGAAAGACTCTA | 9873 |
rs543288498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925258 | CTTACCATAATCAGG[A/G]TCATTTCTGATTATA | 9873 |
rs543306817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872507 | TGTCTATAAAGATTT[A/G]CCTATTCCAGACATT | 9873 |
rs543321527 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864224 | ATGTAAGCAATAAAA[C/G]AACAGGGTGGGCATA | 9873 |
rs543330651 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973090 | TGGGTAAGTTATGGC[A/C]GGGCGCGGTGGCTCA | 9873 |
rs543338214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971172 | ATAAGTAACTGGAAC[A/G]GGTCAAAATATAAAA | 9873 |
rs543344445 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023109 | AACATTTAGAAGAAC[-/A]GAGAAGAAAATCTCC | 9873 |
rs543383159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856300 | GAGAAGTCAGGATAT[A/G]ATGAGTCCAAAAGTA | 9873 |
rs543393033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111116 | TATGCTTGAGAATGA[C/T]CCATGTGCTGAGGAA | 9873 |
rs543398352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046651 | TAAATATAGATAGAC[C/T]TCGCTTACAAGGAAG | 9873 |
rs543401010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072236 | AAACAGAAGGTTTGG[G/T]GAGGAAAATAATGGG | 9873 |
rs543418138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001967 | TGCTCCTACACTATT[C/T]ATAAACACAATCGAT | 9873 |
rs543421259 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100234 | GACCATTCCTCTTCG[C/T]GTCCCTTCCTCCCTT | 9873 |
rs543424095 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963832 | GGCTCACCTCCTGCT[C/G]TGCGGCCTGGTTCCT | 9873 |
rs543437999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002732 | TTAATAGCTGTTTGC[C/T]CTTCCAGTCTCAGTT | 9873 |
rs543439310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095678 | CAAGCATACTTCCTG[A/G]GGTAGTAAACTTAAA | 9873 |
rs543441316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994398 | AGGTAGTAGTAGTAG[C/T]AGCAGCAGCAGCAGT | 9873 |
rs543446783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886295 | CATCTCCTTCTTTCC[C/T]ACCTTCATCTTTTGG | 9873 |
rs543446885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895098 | AACTTATTCTGACTA[C/T]GCTAGGATAGCAGAA | 9873 |
rs543464099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064343 | AAAGCAGGAAAGATC[C/T]AAAATTGATACCCTA | 9873 |
rs543479941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011643 | CCCTTCTTGGTGTAG[C/T]GCCATCACACAATCT | 9873 |
rs543498847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117516 | AAATTTCCTTTTGAA[C/T]CATACCCTACAAGTT | 9873 |
rs543499714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003213 | TTTAACAAAATAATC[A/G]TAAGTAGCACACTTC | 9873 |
rs543508614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955420 | CTCCAGGAGGCTCCC[C/T]GAACCCTGTCCTGGG | 9873 |
rs543534344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887056 | ACCTTCCATATGGGG[A/G]AGATTTCCTAAGCTC | 9873 |
rs543560585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033116 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 9873 |
rs543560594 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116931 | TATATTTTTTCATGT[A/G]AAACCTTTCCATTTT | 9873 |
rs543560850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996014 | ATAATAAACATAAAG[G/T]TTATGTAGAAACATG | 9873 |
rs543566870 | in-del | -/TCTA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875348 | GTCAATATTATAAAC[-/TCTA]TCTATCTATCTATCT | 9873 |
rs543583427 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003975 | AGCCAGGCGTTGTGG[C/T]TGGCACCTGTAACCC | 9873 |
rs543583728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124226 | GAGAACACCTGGACA[C/G]AGGATGGGGAACATC | 9873 |
rs543596392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948372 | TTCAAAATTACTGAA[C/T]GTTTCATTTTTCAAC | 9873 |
rs543596845 | snp | A/G | 6.60469e-05 | 0.00574622 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72849875 | GCCTTCTTCTCTTTC[A/G]GTATCTGCATTAAGC | 9873 |
rs543602079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924465 | TTTTTTGTATTTTCA[A/G]TAGAGACGGGGTTTC | 9873 |
rs543606453 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136072 | GGCTGAGGCAGAAGG[A/C]TCACCTGAACCCAGG | 9873 |
rs543608961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841856 | CTCTCTAGGGTTCTA[C/T]TGAAAATGTACCAAA | 9873 |
rs543616331 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949495 | AAGAAAAAGAAAAGA[A/G]AAGAAAAGAAAAGAA | 9873 |
rs543620596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871915 | ATTTTGATTTCCCTC[C/T]GAATTCTCTGCTTGG | 9873 |
rs543621015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033667 | ATACTCAAACTATGG[A/C]ATTCTATACAAATTT | 9873 |
rs543622299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105430 | TACCAGGCTCTTTAT[C/T]TGGTAACATTACTTT | 9873 |
rs543623054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025931 | ACTGATATGCTCCAC[A/G]TTTTGACTAAAAAAC | 9873 |
rs543624383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896952 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 9873 |
rs543629920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872126 | TCATATACGTCTTTA[C/T]ATAAGACAATTGGAA | 9873 |
rs543644444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131961 | TCTTCTCATTTTTTT[G/T]AATCAGTCACTGACA | 9873 |
rs543673941 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028484 | GAAGTAACTAACTTG[C/G]TTTTGATTTTACAGG | 9873 |
rs543676485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916036 | ACACATGGGAACAAC[A/G]CACACTAGGGCCTAC | 9873 |
rs543684419 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026870 | TCGCTCTCTCTCCTG[A/C/T]GACCATGTAAGACAT | 9873 |
rs543686243 | in-del | -/CAAAT | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980907 | GTATGATTAAACCAA[-/CAAAT]CAAATACCCTGCTTT | 9873 |
rs543689279 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906049 | AACTAATTTACACTC[C/T]CACCAACAGTGTAAA | 9873 |
rs543689537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071539 | TACTAAAAATACAAA[A/T]AAAAAAAAAAAATTA | 9873 |
rs543702093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955907 | TTTCCTAGTTCTGCC[A/C]ACTACGGACTCAAAG | 9873 |
rs543702278 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881245 | TTTCTCAAAAGAAGA[A/C]ATAATGGCCAACAGG | 9873 |
rs543703438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018880 | AGTTTTTAAAAATAA[C/T]AGAAGTTTATTCCAT | 9873 |
rs543734023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989162 | AGAAAATGACTTCAT[A/C]CTAAGGACTATACAC | 9873 |
rs543736937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881925 | GGGGGGCGAATCATG[A/G]GGTCAGGAGATTGAG | 9873 |
rs543742186 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944069 | CCAGCATCATCCTGA[C/T]ACCAAAGCCTGGCAG | 9873 |
rs543764470 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010871 | CAGTGAGCTGGGTGG[A/G]TGGGCAGATTCTTGG | 9873 |
rs543775333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135393 | CCTGACTAAAATTCA[A/G]TAATTTTTCCATATT | 9873 |
rs543785302 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042446 | ATCAATACCATGCTG[-/T]TTTGGTTACAATAGC | 9873 |
rs543798939 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910065 | AGGAGCACCTCTGCC[C/T]GGCCGCCCCATCTGG | 9873 |
rs543803411 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888432 | AATGTAATGGGCTAA[A/T]AAGTAAGTGGGAGGT | 9873 |
rs543810781 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978453 | ACCATCAGAGAAACA[A/T]AAATCAAAACTATAA | 9873 |
rs543848982 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056425 | AAATGTAATCTTTTT[A/T]AAAATTATTTTTTGT | 9873 |
rs543851955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006393 | CAGCAACTCAAACCT[C/T]CTAGTAGTTGGCTCA | 9873 |
rs543856534 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056115 | CTTACTATCTTTGAC[A/C]TACAACCTTGCTTCC | 9873 |
rs543865713 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864284 | TAAAAATATGGACTG[A/G]GTGTGGTGGCTCATG | 9873 |
rs543878691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958450 | TGGAACCCAGGAGGC[A/G]GAGGCTGCAGAGAGC | 9873 |
rs543881033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848937 | AACGATTTACATTGG[A/G]AAAAAATGCTAACAC | 9873 |
rs543885922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910530 | TAACCTTACCCCCAA[C/G]CCCATGCTCTTTGAA | 9873 |
rs543890545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860726 | GGTGCTGGGAGGCTG[A/G]GGCATAAGAATCACC | 9873 |
rs543893360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947594 | AGCCACACCACTATA[A/T]TGCTGGTCCTAATGG | 9873 |
rs543897983 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142105 | GGAAGGCTTGGGGCC[C/T]GGGCGGCCCGGGCGG | 9873 |
rs543899306 | in-del | -/T | 0.349699 | 0.22926 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018518 | GGTACAGATCTTGTC[-/T]TTTTTTTTTTTTTTT | 9873 |
rs543904018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104825 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCCTG | 9873 |
rs543908213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057106 | AAAAATAAAATAAAA[G/T]AAATAAATAAAATCC | 9873 |
rs543910309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016029 | AATGATAGGCTGCAC[A/G]TGGTGGCTTACACCT | 9873 |
rs543911195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907318 | TTCCTAATTGAATAC[C/T]CTTTATTTCTTTCTC | 9873 |
rs543951776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899938 | ATGTCATTAATTTAC[C/T]GTATGACTCTGGACA | 9873 |
rs543959935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852208 | ATGGCTATTATTTAA[A/G]AAGTCAAAAAATAAC | 9873 |
rs543969381 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011789 | CTGACTAATCCCACC[G/T]GAACAGGCTACCTTG | 9873 |
rs543971757 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949165 | ACCACAAAAAGAAAC[C/G]TGGCCGGGCGTGGTG | 9873 |
rs543974920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999241 | AATTGCTTAGATGTA[A/G]CATAGATCATCAGCA | 9873 |
rs543980503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108129 | TGGGGTAATATCTCA[C/T]TGTAGTTTTGATATG | 9873 |
rs543999183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897608 | CAACTGTTGTCATTT[C/T]ACACATGAGGAAGCT | 9873 |
rs544007335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988384 | TTCTTTTCCTACTTA[C/T]TCTTAAAAAAAGGTC | 9873 |
rs544008847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052604 | AACACTGTCGAAAAT[A/C]AACAATGAAACAAAT | 9873 |
rs544010720 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941384 | TAAAAACTATACTTA[A/T]ATTATAATTTATATA | 9873 |
rs544025794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844786 | TTACACAAACAAAAA[C/T]AAGGCAAAAAAGGGG | 9873 |
rs544037279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999824 | AAGTTATACTAGTAT[A/T]AATTCTCTGCCCCTA | 9873 |
rs544048651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100101 | ACAGTGGCTGTGACA[A/C]CCCGCTAATCCTCAC | 9873 |
rs544057484 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037824 | CACTTGTTATGCATA[C/G]AGCAGAACCTCAAAC | 9873 |
rs544058634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089401 | GGTTAAACACATCAT[G/T]AGCATATGATCCAAC | 9873 |
rs544060193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933915 | GGAGTTCAAGACTAA[C/T]TTGGGCAACACAGCA | 9873 |
rs544069295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044708 | GCTGGGTAAATACTA[C/T]ATAGAAAACAGTGCA | 9873 |
rs544091900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884391 | GTGATTAGTCAAGAG[G/T]TCTGCTAACATAGCA | 9873 |
rs544093765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893189 | TATTTTTAGTAGAGA[C/T]GGGGGTTTTGCTATG | 9873 |
rs544094637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942061 | CTCAAAATCTCATGT[C/T]GAAATGTGATCTCCA | 9873 |
rs544097569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846230 | GTGTTGCCCAGGCTG[A/G]AGTGCAGTGGTGCCA | 9873 |
rs544102705 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907793 | AGAGACAGGGTTTCA[C/T]CATGTTAGCCAGGAT | 9873 |
rs544117461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038533 | TGAAAAGAATGAAAT[C/T]TTGTCCTTTGTAGCA | 9873 |
rs544119502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119076 | GGAGGCCAAGGCAGA[C/T]GGATAGCTCAAGCTT | 9873 |
rs544129558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885393 | ATACTTGCATTAGAA[A/G]AGGTGAGACATCGTG | 9873 |
rs544157594 | in-del | -/ATG | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884563 | ATATAGTTTATATAT[-/ATG]ATGATATATATAAAA | 9873 |
rs544166742 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122177 | GCTAACTTAAAAGGC[-/A]AAAAAAAAAAAATGT | 9873 |
rs544178976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023268 | ACAAGCTGCAGATTA[A/G]GAAAAAATACTTGCA | 9873 |
rs544180312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913432 | TGCCACCACACTTGG[A/G]TAATTTTTGTATTTT | 9873 |
rs544180482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031407 | CTTGAGGGCGGGAGG[C/T]GGAGGCTGCATTGAG | 9873 |
rs544182850 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118472 | GTTCTGCCTGTTTTA[C/G]AACTTTTCAGTATAT | 9873 |
rs544184510 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864192 | GTGATGTTAACATTG[C/T]GGGCTATAGTTTGAA | 9873 |
rs544199323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034012 | TAGACAATTTTAATA[A/C]CGATAGCAAATATAT | 9873 |
rs544209367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877205 | TCAGTTTTTTTAATG[A/G]TTAGTGTTTGTTCTC | 9873 |
rs544228025 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875072 | ATAAGTGTAAAGCTA[C/T]AGTTGAATTTCAAGT | 9873 |
rs544236164 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059912 | ACCAAAACTTTGCTT[A/G]TATCTGCAGAAATTC | 9873 |
rs544236272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067629 | GACCTGGTTCTACAT[C/T]AAAGACTTAGGAGCT | 9873 |
rs544263128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126604 | AACTAATACGAACTT[C/T]TATAATATCTGTTAA | 9873 |
rs544271643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908039 | ATCTGACTACCCTTC[C/T]CAGACTCTGGTAAAC | 9873 |
rs544276031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951098 | GCTATCTGAGTCTCT[A/G]AATAACTTCATGAGG | 9873 |
rs544279752 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931520 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCAAG | 9873 |
rs544320838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024190 | TACCAGTGGTTGGGG[A/G]AACCGAAGATAGAAT | 9873 |
rs544321051 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931126 | TTTGAAAAGGAGTCG[C/T]GCTGTGTCACCTAGG | 9873 |
rs544332923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878675 | CTGGAATTGATAATA[C/T]ACTAAATAGATAAAA | 9873 |
rs544333499 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925540 | TTAAAACAAACAAAC[A/C]AACAAATAAATTTCT | 9873 |
rs544340785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852919 | CTGCATGTTCTCACT[A/C]ATAAGTGGGAGCTAA | 9873 |
rs544340863 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969372 | CTGTGCAGAAAAGCT[A/C]GTTGGCATTTAGGTT | 9873 |
rs544342448 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889494 | ACACATATAATGCTT[A/G]AGCAAAGGAGTTTGA | 9873 |
rs544355849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845387 | AGGTTGCAGTGAGCC[A/G]AGATCACACCACTGC | 9873 |
rs544359133 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855476 | GTGAGACTCCATCTC[-/A]AAAAAAAAAGAGTTC | 9873 |
rs544362242 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900548 | AAATTAGTCATAATT[A/T]TAAGACAAGCTTGAC | 9873 |
rs544362933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951776 | TTTTCCCATTGATTT[A/G]AGGTTTACCCTTTCA | 9873 |
rs544365801 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068735 | AACACTTTGGGAGGC[A/C/T]GAGGCAAGAGGACTG | 9873 |
rs544389608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870468 | ACCAATTCTTTCAAG[A/T]TTGGCTCTACCAATC | 9873 |
rs544389994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053389 | GACTACTAATGAAAG[A/G]TAGAAAATGAATTCT | 9873 |
rs544396200 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944502 | CACAAGACAGGGATG[A/C]CCTCTCTCACCACTC | 9873 |
rs544402062 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098361 | GCATATTTTCTGTCC[C/G]CTTCTATTAATTGAT | 9873 |
rs544411012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062039 | CCCAGTAGGGGCCAA[C/T]AGACACCTCATACAG | 9873 |
rs544413122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006657 | TACAGCAATTGCTGC[A/G]CAATCACTTCTTGGC | 9873 |
rs544439461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908894 | CCTGGGCTCAAGCGA[G/T]CTGCCCACCTTGGCC | 9873 |
rs544449320 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133065 | TCAAAGCCACTTACA[A/G]TATCACTTCACATCC | 9873 |
rs544450501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093088 | CTAAGTGACTGAACC[A/G]CAATAAAAACTGCAT | 9873 |
rs544451849 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045048 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 9873 |
rs544455898 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077052 | GAGGCGGAGCTTACA[A/G]TGAGACAAGATTATG | 9873 |
rs544483195 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945121 | AAAAGAACAAAGCTG[C/G]AGGCATCACACTACC | 9873 |
rs544486926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046141 | GACTAAAGACACACA[C/T]CATGATGCCATGCTG | 9873 |
rs544488155 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966907 | AACCCTGATTATGAG[G/T]TAAGAAAGTGGCCGG | 9873 |
rs544491019 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891083 | ACCATACTCAGCTCA[-/T]TTTTTTTTTTTCCTT | 9873 |
rs544492827 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992367 | GATTCAATGCCATCC[C/T]CATCAAGCTACCAAT | 9873 |
rs544497767 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866905 | GGGAAGTTGGGAGGT[-/TA]TAGAGTTTTAGCTTT | 9873 |
rs544498822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108862 | AGGCGTGAGCCACCG[C/T]GCCCAGCCTAGATTT | 9873 |
rs544499820 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980616 | AGTCCTCCAGCAGTA[A/C]GTGATTTCCATCACT | 9873 |
rs544513637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093631 | TTTGAGACCGAGTTT[C/G]GCTCTTGTTGCCCAG | 9873 |
rs544523212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109440 | CAGAGATCTTTCACT[A/T]CATCAGTTAATTCAT | 9873 |
rs544552512 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838538 | CATGAGGGCTGCCCC[C/T]CTCTTTGCTCCTAGG | 9873 |
rs544555948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909478 | TAGGAAGTGAGGAGC[A/G]TCTCTGCCTGGCCGC | 9873 |
rs544560374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984676 | TCAGGCATTCCACAG[C/T]GTGAAGTTTCCGAAG | 9873 |
rs544582730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930622 | TGGTGGTGCCCATCC[A/G]TAGTCCCAATTATTT | 9873 |
rs544586336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102291 | GAATGCTAAATAATA[C/T]AGATAGACTCTGGGG | 9873 |
rs544588514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010182 | GCTTGATCTAGTCTA[C/T]TGTTGAAGCTTTCAA | 9873 |
rs544593149 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069343 | AAAAAGACTACAAAA[G/T]AACTATCCAAAGAGA | 9873 |
rs544609862 | in-del | -/TGTATAATATACTGAA | 0.0341408 | 0.126114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907439 | AATGCTTCCAGTTTT[-/TGTATAATATACTGAA]TGCCCATTCAGTATA | 9873 |
rs544620004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976492 | ACTATGCTGCCCAGG[C/T]TGGTCTCAAACGCTT | 9873 |
rs544636773 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923349 | GGTCATATGATAACT[C/T]TATGTTTAATTTTGA | 9873 |
rs544638146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125668 | CATGACCGCACCACT[A/G]TAACCTAGCCCAGAC | 9873 |
rs544658265 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100322 | GGCACTGACCTAAGC[A/G]CTTTACATGCTTTTG | 9873 |
rs544661598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035179 | ATGTATGTATGTATG[C/T]ATGTATGTATGTATG | 9873 |
rs544674781 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077966 | AGTAAGAGTGAGGGC[A/G]GTAATGGCAGGGAAC | 9873 |
rs544676383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933742 | GCTTAAAGTAGACAA[C/T]TTTTATGTCAAAGCT | 9873 |
rs544701489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133916 | AGGGTTATGGGGAGC[A/G]ACTGCTAATGGGTAC | 9873 |
rs544706234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967947 | ATACAAAAAATTAGC[C/T]GGGTATGGTGGCGGG | 9873 |
rs544713892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024955 | GATACTATCTAACAC[A/C]AGTCCAAATGGCTAT | 9873 |
rs544718837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927180 | TCAGATACGAGCTGC[C/T]TTCCATTTTCTAAGG | 9873 |
rs544726479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862016 | AATATCTGAATAATC[A/G]TCAATGCAATTACAC | 9873 |
rs544748739 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968824 | CCCAAGGTTCATCCT[C/T]TGACCAACACTTCTC | 9873 |
rs544753757 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917405 | TGACCATAGATGTTC[A/G]GGTTTATTTCTGAAC | 9873 |
rs544760096 | in-del | -/TTTTTTTTTTTTTTTTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916986 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTT]GAAGCAGAGTGTTGC | 9873 |
rs544786891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854338 | ATGTCCATTGAGAGA[G/T]GAATGGATAAGTAAA | 9873 |
rs544787011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141391 | AAGCAGGCCAAACCC[C/T]AAGGCTAGGCTAGAA | 9873 |
rs544801818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111654 | TATTTTTGGGTGTGT[A/G]GTCATCTCTTCCTTC | 9873 |
rs544824453 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898805 | TGTGATCACGGCTCA[C/T]TGCAACCTCCACCTC | 9873 |
rs544826330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111603 | AATCCATTTACATTC[A/C]ATGTTGTTACTGATA | 9873 |
rs544829734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909193 | AGGCACACGCCGCCA[C/T]GCCTGACTGGTTTTT | 9873 |
rs544852572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140612 | AATTACTCCATAATG[A/G]CTGCGAAAAAGCACA | 9873 |
rs544855637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118373 | TATCATCCCAAAAAG[A/T]TTCCTCATGCCCCAT | 9873 |
rs544863380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020496 | AGTGATCTTTTAACA[A/T]TGAACAAGTTCACTG | 9873 |
rs544872267 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058037 | GGCGCCCACGACCAC[A/G]CCTGGCTAATTTTTT | 9873 |
rs544882465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066095 | CATCACGCTACCTGA[C/G]TTCAAACTAGGGCTA | 9873 |
rs544913461 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911721 | AGGGTACATGTGCAC[A/T]ATGTGCAGGTTAGTT | 9873 |
rs544916755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125588 | CACACATCTGTAGTC[C/T]GAGCTACTCAGGAGG | 9873 |
rs544916792 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117820 | CCATTAATTAATCCA[A/C]CTTATTTTTGGTGTC | 9873 |
rs544918826 | in-del | -/ATGTAGTGTAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081736 | ATTTTATAAATATAT[-/ATGTAGTGTAC]ATGTATGAAAGTGTA | 9873 |
rs544929183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110188 | GGTCTTTGGTATCAG[C/G]GTACTGCTGGCCTCA | 9873 |
rs544941248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949373 | GAGAATCACTTGAAC[C/T]CTGGAGGCAGAGGTT | 9873 |
rs544950236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905710 | TTTCTGTCCTTGTGA[C/T]AGTTTGCTTAGAATA | 9873 |
rs544968267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855415 | CGGGAGGCGGAGGTT[A/G]CAGTGAGCCAAGATC | 9873 |
rs544972325 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873329 | TGAGACTCTGTTTCA[-/A]AAAAAAAAAAAAAAT | 9873 |
rs544978013 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942316 | AGGCCTCACCAGAAG[C/G]AGATGCCAGCAGCAT | 9873 |
rs544980557 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870527 | GTTATAAACTACTGT[C/G]TCTCTTTAATAATAA | 9873 |
rs544982271 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089263 | ATGATATTAATGGAT[A/G]CTATAATAAAACAGA | 9873 |
rs544987923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949804 | GGGTTGTTTCCACCT[C/T]TGGATTGTTATGAAT | 9873 |
rs545022936 | in-del | -/C | 0.000816493 | 0.0201886 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097634 | TTTTTTTTTTTTTTT[-/C]TAATTACTGATTCAA | 9873 |
rs545044023 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067910 | AAAAGAGGATTAATG[A/G]ACTGATAGTTCCATG | 9873 |
rs545046140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027696 | CATTTCAGAGATGTT[C/T]GCTGCACTCCCCGCC | 9873 |
rs545072411 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903471 | TGATCCACCGGCCTC[A/G]GCCTCCTAAAGTGCT | 9873 |
rs545074194 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873654 | TAAGAAACTAATCCA[A/C]GGCCACAAAGACTTA | 9873 |
rs545097204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099265 | CCACTAGGATGGCTG[G/T]AAAACAACACAAAAC | 9873 |
rs545097529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091522 | CCACTGCACTCCAGC[C/T]TGGGCCACAGAGTGA | 9873 |
rs545106599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997770 | CAGTGGCACGATCTC[A/G]ACTTCCTGCAATCTC | 9873 |
rs545116211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971392 | AGTGTCAGTAGAACA[C/T]AATCACTCTTGTGAT | 9873 |
rs545117588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964089 | ATGGATGATACAAAC[A/C]TGGATAATATAGTTA | 9873 |
rs545138076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910778 | TATTATCCTATGACC[C/T]TGCCACATCCCCCTC | 9873 |
rs545141367 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043033 | CTCTTTTCCTATTTA[G/T]ATGCCTTGAATTTCT | 9873 |
rs545160649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092076 | TATGATCTCATCTGA[A/G]AAGCCTTCCTGAATT | 9873 |
rs545162435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857238 | AGAATAATTTCTTCC[C/T]TTTTCCTCTTCCACT | 9873 |
rs545173776 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040235 | TTATGCAAATGCCAA[C/T]CAACCCAGCTCTTTT | 9873 |
rs545190229 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069724 | GATACAAATAATGTT[A/G]AAGAAGCAATATTTA | 9873 |
rs545198293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866148 | CAAGTGGGCCTGGAA[C/T]TTGCTGTCATCAAAA | 9873 |
rs545205614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972160 | TCTGCTTCAGTACCC[C/T]TCATCTATTGTTGAT | 9873 |
rs545237433 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107152 | TTGATTCTCAAGACT[C/G]TCCGCAATTCTTGAG | 9873 |
rs545239664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139565 | ATAAACACACTTCTC[A/G]CTAAATTTGGCACTC | 9873 |
rs545267298 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969628 | ACATTAAAAGACTAG[A/G]AAAAAGCCCAAATGT | 9873 |
rs545271827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012963 | TCAAATATGAGATGA[C/T]GAGGAATTAAATTCC | 9873 |
rs545276787 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099882 | GCCTCTCGGTCACTC[C/T]GAGGGGACTTTCGGC | 9873 |
rs545282278 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932270 | TATTGCAGCAATCTT[C/T]TGTTGCCCTGCATCC | 9873 |
rs545288450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875434 | GTGGTGCAATAATAG[C/T]TCACTGTAACCTTGG | 9873 |
rs545289682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974175 | CGTTTATTTGGTTCA[C/T]GGTTCTCGGGACTGG | 9873 |
rs545296770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084221 | ACAATGTGAAAATCA[A/G]ATTTTGATTGGCTTC | 9873 |
rs545297143 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105619 | TCTGAAGATTAAGTA[A/T]AATAAATGGATATAA | 9873 |
rs545310469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857919 | TGGGTTTGAATGTTG[A/G]CTATGTCACTTACTT | 9873 |
rs545310548 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035678 | TTTTAAGTACTGAAC[A/G]GTACTGAAATGTTCA | 9873 |
rs545329404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013688 | TGAGTTCTTAGCACA[A/G]TGTCTGCCACATAGT | 9873 |
rs545333321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004338 | GGAAATAGCACCTCC[A/G]TGGTCATAACCTAGA | 9873 |
rs545354934 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906183 | TCTCTGATGACCAGT[C/G]ATGATGAGCATTTTT | 9873 |
rs545390126 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897891 | TTCAGCAAAAAAGAT[G/T]TATTTTACTTTTTCT | 9873 |
rs545392085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005318 | ACTTTAGTGTCTACC[A/G]CTCTTCTGAAATTGC | 9873 |
rs545407997 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966217 | CAGGAAGGAGTGCAG[A/T]GGTGCGATGTCGGCT | 9873 |
rs545425143 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889465 | CTGCTGAGTGTTGAG[A/C]AAGTACAGAAAAAAC | 9873 |
rs545440808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072355 | ATGTCCCCAAGAGTA[C/G]TAACATTTAATTATA | 9873 |
rs545451536 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000236 | TAAAATATTATTTCC[C/G]GAAATAATTACTTTA | 9873 |
rs545472967 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838727 | AAAGGTGCCTAAAAA[A/T]CAAGACTGGCCAAAC | 9873 |
rs545507178 | snp | C/T | 2.35691e-05 | 0.00343278 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889991 | TATTGCTATCCTTAT[C/T]GTAACCACTACTGCT | 9873 |
rs545517758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043744 | TTAAGAGATATGATA[C/T]GTGTTACATTCAGTT | 9873 |
rs545537336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839475 | AGACTTTTGTAATCC[C/T]CTGAATGAGAGTTGA | 9873 |
rs545539659 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140827 | CTCGCCCGCCAGGCC[-/G]GGGGCCCCAGGGTTC | 9873 |
rs545546372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083448 | CAGCTACTCAGGAGG[C/G]TGACACAGGAGAATC | 9873 |
rs545550408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035963 | TGACCTTGTGATCCG[C/T]CTACCTCAGCCTCCC | 9873 |
rs545550551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990754 | GCCCACAAGAGAAAG[A/C]AGGAAAGATCTAAAA | 9873 |
rs545581545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936533 | TACTCCCAGCACTTT[G/T]GAAGGCCAAGATGGG | 9873 |
rs545600639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986504 | GTGAGCCACCGTGCC[C/T]GGCCCCAATTATTTT | 9873 |
rs545614494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046424 | GAATATGTCTGAATA[C/T]CAATTTTCATAGAAA | 9873 |
rs545634626 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876235 | TTCGGGAGGCTGAGG[C/T]GGGAGGATTGCTTGA | 9873 |
rs545644187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919361 | GGAGTGAGATACTCA[C/T]ATGAGTGAATGCAGA | 9873 |
rs545676699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029421 | GATTTGGAGAGTAAA[C/T]TACAGTTAATTTAGG | 9873 |
rs545677053 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092827 | ACAGTAAAGGATTAA[A/C]CCTACCCAAAGACAG | 9873 |
rs545685562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866541 | TCCCAAAGTGCTGGG[A/G]TTACAGGTGTGAATC | 9873 |
rs545703127 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999815 | CTGGTTGGGAAGTTA[C/T]ACTAGTATTAATTCT | 9873 |
rs545748808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120583 | AAAAATACAAAATTA[A/G]CCGGGCGTGGTGGTG | 9873 |
rs545760547 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067015 | TTATAAATCATTCTA[A/C]TATAAAGACACATGC | 9873 |
rs545765176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130164 | CAGGTGTGAGCCACC[A/G]CGCCTGGCCCATAAT | 9873 |
rs545768586 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021458 | AAACTAATGCAAGAA[C/G]AGAAAACTAAATAAT | 9873 |
rs545774371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017744 | CATTGCATGAAAATA[C/T]CTTCTAACCACTCCT | 9873 |
rs545774448 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091837 | TTGAGGTCAGAAGTT[C/T]GTGACTAGCCTGGCC | 9873 |
rs545778144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879403 | AAAAACTTAGTAGGT[A/C]TTTGAAAAGCAGAAA | 9873 |
rs545779382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901478 | TACAGACAGAAAGTA[G/T]ATTAATGATGTCAGG | 9873 |
rs545784873 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130961 | AATTCTCCCTCTCAA[G/T]ATTTACAACATTTTA | 9873 |
rs545787717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054448 | GATGGGCATGTAAAC[C/T]CTTCAATGTAGTCTC | 9873 |
rs545817371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893333 | ACATTTTTCTTTTTG[A/G]AAGACAGGTTCTCAC | 9873 |
rs545819752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863530 | AATTAAAAATTTGTG[A/C]TCTTTGAAAGGTATT | 9873 |
rs545825638 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963899 | GTTGGGGACCCTGGA[A/T]TAGATGACAACTCTG | 9873 |
rs545829110 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924184 | GGGTTCCAGTAATCC[A/G]CCTGTCTCAGCCTCC | 9873 |
rs545833265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080248 | ATTACACTAAGCTAT[A/G]ATTGTGCCACTGCAA | 9873 |
rs545868115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113610 | TTGTGGATATTTGTC[A/G]GTGTCCAGGCATTGA | 9873 |
rs545881438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864178 | CTGAAAACGGGGAAG[C/T]GATGTTAACATTGTG | 9873 |
rs545886724 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045761 | CATCACACTCTGGGG[A/C]CTGTTGTGGGGTGGG | 9873 |
rs545888765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959513 | GTGCTGGGATAACAG[C/G]CGTGAGCCACCACGC | 9873 |
rs545894055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939010 | CTACTAAACATGTAA[C/T]GCAGGATATTTTCAA | 9873 |
rs545898853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970357 | TCTAATGTATGAAAA[C/T]TGTCTTTTATCTAAA | 9873 |
rs545899648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010709 | TGCAGTTATTAGTGG[A/G]GCCTGTGGTAAAGTT | 9873 |
rs545914739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033414 | GGACAAGTTTTAGTG[C/T]AAAGAATTTTAGAAT | 9873 |
rs545932522 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002900 | TTAACATCTGTCCCT[C/G]TCACTATAGTGAAAG | 9873 |
rs545935555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962828 | AGCAATTAGAGTCAA[C/T]AGATTACAGAACTGC | 9873 |
rs545954415 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994126 | ACCAAACAGAATAAC[C/T]GGTCAGCTATGTGGA | 9873 |
rs545959286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002652 | AGAAAGAGAGGAAGG[C/G]AGATACCCTTCATCC | 9873 |
rs545962088 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909996 | CACCTCTGCCCGGCC[A/G]CCCCATCTAGGAAGT | 9873 |
rs545982504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856103 | GCCTTCATAGGAGAG[A/C]CATTACATTAATTAA | 9873 |
rs545993573 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878878 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACTTGAG | 9873 |
rs545997545 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922262 | GGTGTAGGAGTTAAG[A/T]GAAATAATAAACGTG | 9873 |
rs546015473 | snp | A/C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100476 | TCAAGCGATTCTCCC[A/C/G]CCTCAGCCTCCCAAG | 9873 |
rs546017847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931626 | AAAAATTAGCCGGGC[A/G]CAGTGGCAGGCATCT | 9873 |
rs546018019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040151 | CTGAGTTCATTTGTT[C/T]TGGACAGGTGGCCAG | 9873 |
rs546018892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003095 | AAAAGAGACCTTTAG[A/G]GTTTAGCAGATTTAT | 9873 |
rs546025217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954276 | AGTGGCACAGCATGG[C/T]GGCTCACTGCAAGCC | 9873 |
rs546034005 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953844 | TGGCATTAAGAGCTT[A/G]CTTGAGGAAACATCA | 9873 |
rs546045887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848808 | TCTGGGACGTTCAAG[C/T]AAATATAATGGGAGG | 9873 |
rs546048421 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143945 | CACCAGAATCCTTAA[G/T]CAAATCAGGGAAGGC | 9873 |
rs546052592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137363 | CTTGGAGCACCAACA[A/G]TCTCTGTCTTTACAT | 9873 |
rs546054576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932389 | ACTGGCTACTCATCA[A/C]ATTTAGGAAAAGGCT | 9873 |
rs546057521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041016 | TTATTTCGCTTAACA[C/T]AATGACCTCCAGTTC | 9873 |
rs546062898 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098473 | TCTAACATATGATCT[A/G]TCCTGGAAAATGTTT | 9873 |
rs546065257 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928257 | AAAAAAATTCCACAA[A/T]ATTTTTTTCAATGGC | 9873 |
rs546077162 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031471 | ACAAGACCCTGTCTC[C/T]GAAAAAAAAAGAGAG | 9873 |
rs546077998 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896889 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 9873 |
rs546080755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033010 | AGTACTTAGATTGGC[C/T]GGGTGCGGTGGCTCA | 9873 |
rs546085146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057038 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCTA | 9873 |
rs546117842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104773 | GGGGTTTCACCACCA[A/G]GCCAGGCTGGTCTCA | 9873 |
rs546122866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041710 | TCTCTTCACTATGTT[A/G]ACTGTTTCTTTGATG | 9873 |
rs546124094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135368 | AAATGAACAAACATG[A/G]TAATATCCACCTGAC | 9873 |
rs546136533 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060798 | CTAGGTTAAGAAGAA[C/G]GCAATGGAGAGTTTG | 9873 |
rs546143883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905422 | CCTTACTTTGTATTA[C/T]AAAAAATCCAATTAT | 9873 |
rs546175105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995673 | CATGCCACTGCACTC[C/T]AGCAGGGGTGACAGA | 9873 |
rs546178343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848710 | TGGGATATGCCAACA[A/G]AGGGAATGTTGAATG | 9873 |
rs546181131 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142528 | GGCACGGGGCTTCGT[A/T]CCGCGGCAGGGGAAG | 9873 |
rs546207620 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127358 | CTAACAAAATGAAAT[G/T]AACAAAAATACCAGC | 9873 |
rs546221975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909673 | TGGGAAGTGGGGAGC[A/G]CCTCTGCCTGGCCGC | 9873 |
rs546241357 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883095 | GGAACAACTGGCTAT[C/T]TGTATAGGAAAAAAC | 9873 |
rs546260203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916449 | TCCCGAGTAGTTGGG[A/G]CAACAGGTATGCAGC | 9873 |
rs546272149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120253 | TTACATCCTTGTATA[C/T]TTATTGAACTATGGA | 9873 |
rs546280300 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954102 | ATAAAGGTAGGGGTG[G/T]GAGTAGAAAGCCAAT | 9873 |
rs546281242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848320 | CATTTCCTGAACACC[C/T]CACACTCTCATCACA | 9873 |
rs546282962 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852847 | TTCTGTAGGAACATG[G/T]ATGGAACTGGAGCCC | 9873 |
rs546289491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110973 | TTCCATGTGGTTATA[G/T]AGTTTCCAAAATTAT | 9873 |
rs546290042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127002 | GAGATTGCACCACTG[C/T]GCTCCAGCCTGGGAT | 9873 |
rs546300665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063449 | AACAATATTAACCTT[A/C]AATGTAAATGGGCTA | 9873 |
rs546317190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962065 | ATCTTCAATTTTAGT[A/C]TTAGAGTTTCTTCTA | 9873 |
rs546322049 | in-del | -/AAAC | 0.088267 | 0.190637 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868694 | GACTCTGTTAAAAAC[-/AAAC]AAACAAACAAACAAA | 9873 |
rs546323657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004727 | TGTGGCTGGAGAAAA[A/G]GATAATTACGTTGCC | 9873 |
rs546326626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911580 | CTGCTTTGGGTAGTA[C/T]TGACATTTTAAGAAT | 9873 |
rs546335273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042668 | GGTCATGTTAACAAT[A/G]TTCATTCTTCCAGTC | 9873 |
rs546340346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949448 | AAGAGCAAAACTCCA[C/T]CTCAAAGAAAGAAAG | 9873 |
rs546346166 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887684 | GACTAGTAGCCATAA[-/T]TTTTTTTCATTTATT | 9873 |
rs546350851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104243 | TTTACTTTGCTTCTC[C/T]TAAACAGAAAAGATG | 9873 |
rs546355293 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074250 | TAGAAAAATAAACTT[C/T]TCTATATGGATTTTC | 9873 |
rs546375758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935300 | AGTAAGAACTTTAAA[C/T]AGTCCCCTCCTTATT | 9873 |
rs546390177 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098541 | GGGTGGAGTGTTCTA[C/T]ATACACCTGTTGGGT | 9873 |
rs546391236 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132283 | TTTCCACTAATAACA[A/G]TAGCTACCAATGCTA | 9873 |
rs546392775 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015103 | CCTGCCTTGGCCTCC[C/G]CAAGTGCTGGGATTA | 9873 |
rs546398465 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043236 | TGTTCTTTCTATGCC[A/C]AGTCTGTTGAGAGAT | 9873 |
rs546404971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947492 | TCACATAGGAATTGA[A/C]CACAAGATCTTATTC | 9873 |
rs546410257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995090 | TAATATGTGGCCTTA[C/T]GTTTCTCACTTCTTT | 9873 |
rs546425945 | snp | A/C | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942625 | TTTCTGTACTTTTCA[A/C]ATTTTCTTCTGGTAC | 9873 |
rs546442634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889543 | GGCAAGACCCTATCT[C/T]TACAAAAAATCTAAA | 9873 |
rs546451244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940682 | AAGGTTACATTATAT[A/G]TAGGATTCATGTTCA | 9873 |
rs546456313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096522 | TGCTGCTGCACTCCA[G/T]CCTGGGTGGCAGAGC | 9873 |
rs546456548 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999176 | AGGTTTCTTTCATTT[A/G]CTATCTCAGAGTCCT | 9873 |
rs546459933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036245 | TACAATTAGAAACAT[C/T]AAAGTATTGGAGCCA | 9873 |
rs546462501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126858 | GCCTGACCAACATGG[A/C]AAAACCCTATCTTTA | 9873 |
rs546479001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882216 | GGGAGGCCAAGGCGG[A/G]TGGATCATGAGGTCA | 9873 |
rs546487702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933285 | GCCTATCCTTCCCAC[A/C]AAAGTTATTCTTCCT | 9873 |
rs546493264 | in-del | -/A | 0.0193772 | 0.0965046 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901690 | GTATTCTGCTACCAT[-/A]AAAAAAATGGCAGAG | 9873 |
rs546496104 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058005 | CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGACTAC | 9873 |
rs546496996 | snp | C/T | 3.6632e-05 | 0.00427957 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841000 | ATTTTACTTGAGTTG[C/T]TGAGCAATAATGCTG | 9873 |
rs546499177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987710 | TCCACTGTGCTCATG[C/T]TCATCCTGTGGGCTG | 9873 |
rs546513744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091673 | AGGCTCATGCTTTCA[C/T]GTTCTAGCAAATGTG | 9873 |
rs546515511 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851557 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 9873 |
rs546517331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096941 | TACTGAGATAATCAT[A/G]TGGTTCTGTCCTTCC | 9873 |
rs546525271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036942 | TTCATCTGTTAACGC[A/G]GATCTGTAATTAGAT | 9873 |
rs546528777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912011 | ATTTTGTATCCTGCA[A/G]CTTTACTAAAGGTGT | 9873 |
rs546538806 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099073 | AAAAATTAATTAGTC[A/G]GAGGTAGTGGTACAT | 9873 |
rs546547862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074842 | ACTTGAGCTCAGGAG[G/T]TCGAGGCTGTAGTGA | 9873 |
rs546605506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062923 | CCAATATTCAAATTC[A/C]GGAAATACATAGAAC | 9873 |
rs546610095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029120 | GTAGTACACTAAAAA[C/T]GATAAAATGCCATTG | 9873 |
rs546617260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075308 | CATTCCTTAGGTAAA[C/T]ACCCAATAGAACACA | 9873 |
rs546619086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920758 | ACATACTACATAGAT[A/T]CCTCAATTAATGTTT | 9873 |
rs546624649 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135311 | CTTCAACAATATAAT[A/T]CACTTCATTTCACTG | 9873 |
rs546629435 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058393 | GACATGGTATGGCTA[G/T]ATGTCATCACAATTT | 9873 |
rs546642365 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956765 | CTCAACATATGAATT[C/T]TGGGGAAACTTCAGA | 9873 |
rs546642390 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107706 | CGTGCAAATTTATCT[C/T]TTCTGTGTCTGGCTT | 9873 |
rs546664284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883804 | AGGCATGGTGGAGTG[C/T]GCCTGTATTCCCAGC | 9873 |
rs546667366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919654 | TTAGCTATCTGTTAC[A/G]ACTATAATGTTTCCT | 9873 |
rs546668634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096609 | TTCCAGATAGAATTA[C/T]AGAATGTCAAACACA | 9873 |
rs546680568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067240 | ATCACAACAGAAAAC[A/G]AAACACTGCATGTTC | 9873 |
rs546690559 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056145 | CCTAAGTGTCTTACT[C/T]ATCTGGACCAGCAGA | 9873 |
rs546690774 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092174 | GCTCCATCACTAAGG[C/G]TGGAGTACATTGGTG | 9873 |
rs546704088 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913118 | CTCACTCACTACCAA[C/G]AGAACAGCAAGGGGG | 9873 |
rs546723654 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958847 | ACAAAATTCAGACTC[C/T]TGTTTCATAAAAGGA | 9873 |
rs546730125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098469 | ATAATCTAACATATG[A/C]TCTATCCTGGAAAAT | 9873 |
rs546743019 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997902 | GACGGGATTTCACCA[C/T]GTTGGCCAGGCTGAT | 9873 |
rs546745223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067855 | GTCCATTTTCACACT[A/G]CTGATAAAGACATAC | 9873 |
rs546758851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943246 | GATCTGCCCACCTCT[A/G]CCTCCCAAAGTGCTG | 9873 |
rs546766351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950455 | CCTCAAAGAGTTTTA[C/T]ATAGTTTTAGCTCTT | 9873 |
rs546777640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859373 | TCTCGGTTATCCCAA[C/T]TGACTGTCACCATAT | 9873 |
rs546790116 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118673 | CTTCATTACTGATTT[A/C]TATTTTCATTGCATG | 9873 |
rs546790890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098871 | TGCATTCCTAGATGG[C/G]AAACCAAAAGCACAA | 9873 |
rs546810885 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959473 | ATCTCCTGACCTCAT[A/G]ATCCGCCCGCCTCGG | 9873 |
rs546818710 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942289 | CCTTCTGCCATGATT[A/G]TAAGTTTCCTGAGGC | 9873 |
rs546860339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990325 | CCTGGTAGGCAAACT[A/G]CATCAATTTGGGATA | 9873 |
rs546866893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141739 | CAAGTCGGTGACAAG[A/C]CCAAGACGAGGGCGG | 9873 |
rs546875266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092268 | AAGTAGCTGGGACTA[C/T]AGGTGTACACCACCA | 9873 |
rs546892677 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837700 | GCGCAATCCTTCAGT[C/T]CTTTCTCATAGAAAG | 9873 |
rs546896239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052159 | GTGATCTGAACATGA[A/T]GGTGCTGTGAAGGAA | 9873 |
rs546897172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982186 | AAAACGTTTTTGCAA[C/T]AGGATACTTCTTAGT | 9873 |
rs546898764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100275 | CCCTTCTCCTATTAA[C/T]AACAACAATTAACAG | 9873 |
rs546920649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908296 | GTTGATGGACACTTA[A/G]GTTGCTTCTAAATCT | 9873 |
rs546939221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943962 | AACTTTAACTTCTAT[C/T]GCATGACATGGAGGT | 9873 |
rs546955215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891294 | TAGAAATTGATAAAC[C/T]GGATTTTAAAAATTA | 9873 |
rs546956177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078865 | TACGACTAGAGGCAT[A/G]CGTCACCTCGCCTGG | 9873 |
rs546971436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029620 | GGAGGTGCAGACACA[A/G]AGGTAGGAAGTCATT | 9873 |
rs546976490 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946711 | ATAGCTACCATTTAC[A/C]GAATATCTATTATAT | 9873 |
rs546981442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974655 | CAGAATTTTAAAATG[C/T]ATTTATTTTTAGTTA | 9873 |
rs546982761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932567 | GAGCTTTCACACAGG[C/T]TTTTCTTCTGCCTTG | 9873 |
rs546992185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990896 | AGACACAAAAAAACC[C/T]TTCACAAAAATCAAT | 9873 |
rs547004494 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085801 | TTCAAGTTGATGTTT[-/A]AAAAAAAATGAGAGC | 9873 |
rs547010245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021966 | GGTCTTAGCTACTTT[C/T]GTGTATGGCAGGAGA | 9873 |
rs547013467 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025070 | GCTCAGGCATTGTGG[A/G]AGACTGTCATGATTC | 9873 |
rs547020105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871432 | TTGCTTAGCAAGTAA[C/T]GCATTCAGCTTCATT | 9873 |
rs547028531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876650 | TATTCTACTCATATG[C/T]AGTGGAGTTCGATGA | 9873 |
rs547053247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867782 | TCTTTTTAAAAAATT[C/T]TGGCTATTATTAAGT | 9873 |
rs547066789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868268 | AAACCAAACACTCCA[C/T]GTTCTCACTTGTAAG | 9873 |
rs547075919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033223 | AACCCGGGAGGCGGA[A/G]GTTGCAGTGAGCTGA | 9873 |
rs547078315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008686 | TTAAATTTATCCCAT[C/T]GGCAAGGAAAAACAA | 9873 |
rs547081894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071160 | CATTCTGGAGCTGCT[C/T]TAACTAGCTAATACC | 9873 |
rs547086209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978779 | TGTAAGTTTCCTGAG[A/G]CCTCCCCAGCCATGC | 9873 |
rs547088835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913683 | TCTCCTTTTTCACTT[C/G]TGATTTTATTTATTT | 9873 |
rs547091456 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850006 | CCTTTTAACTCTGCA[C/T]AGAAATGACTATCTT | 9873 |
rs547122485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962377 | CAAATACATTAAATA[C/T]CAATAAGTATAACCT | 9873 |
rs547134476 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014998 | ACAGGTGCCCGCCAC[A/C]ACACCTGGCTAATTT | 9873 |
rs547147296 | in-del | -/ATC | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970402 | AGGTAATGGAAAAAT[-/ATC]ATGTGTTATAGAAAA | 9873 |
rs547164723 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142257 | GGTCGGCCGCCTGCG[C/T]CGCCGCTCCCGGCGG | 9873 |
rs547171209 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907504 | TTATTTTGAGATATG[G/T]TCCAACAATACCTAG | 9873 |
rs547186685 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997631 | TGTACCAGAAATATG[G/T]AATGTAGTATTTAAA | 9873 |
rs547189216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061070 | CTCCCAGCAAGATCC[C/T]CGCAGAAGGCAGATG | 9873 |
rs547189536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125869 | ATAAAACACTTCTTT[G/T]AGTAAAACAGAGCAA | 9873 |
rs547190580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863716 | AAGAAAATATACAGA[C/T]GCAAATAAACATATG | 9873 |
rs547197774 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006682 | CTTGGCCCTCTGTAT[G/T]CTCCCTACTATGCTT | 9873 |
rs547199252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852485 | GGTGGTGCCAAAATG[A/G]CGAAACCTTGTCTCT | 9873 |
rs547203557 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862682 | ATGCAGTCATCATAA[-/T]TCCTAATAAAAATCC | 9873 |
rs547209700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961503 | TCAAGTGATTCTCCC[A/G]TCTTGGCCTCCTAAA | 9873 |
rs547214419 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963152 | GTTTTTAAAAAAATA[C/T]TGTCTTTGTTTCACT | 9873 |
rs547219290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108296 | GCTCATTACATATTC[C/T]AGTTACTAATCCCTG | 9873 |
rs547245435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954985 | ACTCACCACTCAACA[A/C]AATACTTCTGACTTC | 9873 |
rs547251944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052804 | GATGCTAATAGCATG[A/G]AAAGATCAGTTTCTA | 9873 |
rs547252482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115070 | CAATTTAGCCTGCAG[C/T]GGCAAGGCGTGCTGA | 9873 |
rs547271105 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955981 | TAAATATCATCCTCC[A/G]CTAAAAGGAAACAGG | 9873 |
rs547275684 | in-del | -/GTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100376 | GTTGTTGTTGTTGTT[-/GTT]TTGAGATGGAGTTTC | 9873 |
rs547276147 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123766 | CAAATGCAGTCTAAA[C/T]AGAGCTGCCTTTTCT | 9873 |
rs547276478 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880710 | CCCTTGAGCCCAGGA[A/G]TTCGAGACCAGTCTG | 9873 |
rs547288674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063739 | CAGCAAGAAGAGCTA[A/T]CTATCCTAAATATAC | 9873 |
rs547289366 | snp | C/T | 0 | 0 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840699 | GTAGATTAAATGTCC[C/T]GAGATGAGTTGATTT | 9873 |
rs547302453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855897 | TACATCTATACTCTT[G/T]GAACTATTAGAATAT | 9873 |
rs547302943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104414 | AGCTGGGATTACAGA[C/T]GCACACCACCATGCC | 9873 |
rs547314712 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950387 | GTGTTTTTGGTGATA[C/T]CTGAGAAACTGTTGC | 9873 |
rs547317270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944736 | TGTGCAAAAATCACA[A/G]GCATTCTTATATACC | 9873 |
rs547325925 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119040 | GGCGCGGTGACTCAC[A/G]TCTGTAATCCTACCA | 9873 |
rs547326220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111195 | GGTCCATTCGGTCTA[C/T]AGTACAGATTAAGAG | 9873 |
rs547333004 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986080 | AGCAGCCTCTTATTT[C/T]TCTAACAAGAGAAAA | 9873 |
rs547341194 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977812 | GCAATCCCATTACTG[G/T]GTATATACCCAAAGG | 9873 |
rs547342347 | in-del | -/CA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845462 | AAAAAAAAAAAAAAA[-/CA]ACAACAAACAAACAA | 9873 |
rs547361381 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924096 | GAAAGTTTCTTTTGA[C/T]GTACAAAAGTTTTAC | 9873 |
rs547388303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986770 | GGTAGGTATTAGTGA[C/T]AGATAGAATAAAATA | 9873 |
rs547388444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878962 | AAATACAAAAAAAAT[C/T]AGCTGGTTTTGGTGG | 9873 |
rs547414706 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025276 | GGATAAAGAAAATGT[C/G]GTATATATATACCAT | 9873 |
rs547419584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947887 | TTTTACATATTATTT[A/G]TGATTCTCATTTTAA | 9873 |
rs547426990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871018 | TTATGATGTGGCTGG[C/T]AGAAATAGCAGAGAT | 9873 |
rs547427070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879690 | AGGTTTTAATAGACA[A/C]TAATAATAACTCATC | 9873 |
rs547433969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896502 | TACATAGGGCAGAGA[A/T]GTTGAAAAGTACAAG | 9873 |
rs547457366 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940940 | GAAGAAATCCTGACA[A/C]CCAATGGATCACCAA | 9873 |
rs547468426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988473 | ATATATACACTAGAT[C/T]TTTGTGTAAAAGAAA | 9873 |
rs547472452 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880590 | ACCATATATAAAAGT[C/T]GGCTCAAAATGATTA | 9873 |
rs547475472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026131 | GGTGTGTGCCACTGC[A/C]CCCAGCTCATTTTTT | 9873 |
rs547476261 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906274 | CACTTTTTGATGGCG[C/T]TGTTTTTTTCTTGTA | 9873 |
rs547483419 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115616 | GAGAGAGAAGGCAGA[G/T]AGCTAGACACAGACA | 9873 |
rs547504717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136748 | AAAAACCCAAGTTCG[C/G]GCCAGGCGCAGTGGC | 9873 |
rs547521724 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888440 | GGGCTAAAAAGTAAG[C/T]GGGAGGTGAGATTCT | 9873 |
rs547560553 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144074 | CTCAGCTCCACCACC[A/T]ATTTATTGTGAAGCG | 9873 |
rs547569192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909803 | CCTCTGCCCGGCCGC[C/T]CCGTCTGAGAAGTGA | 9873 |
rs547586322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055581 | AATAATATTTATTTC[A/G]TTAAGATTTTATGCA | 9873 |
rs547591820 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122579 | TTAAATTTCCTTTGT[C/T]AAATCAAATAGGCAA | 9873 |
rs547612539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034806 | TTTGACCAGAACTTC[A/G]AAGCAGCAAAAGAAA | 9873 |
rs547644779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980506 | TAACGAGGATAACAA[A/C]GAAAATGAGAAAGGA | 9873 |
rs547646169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910118 | GGCCACCCATCGTCT[A/G]GGAAGTGAGGAGCAC | 9873 |
rs547652239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121732 | TGCCACTGTAAACAA[C/T]AGCTATAATTTATAA | 9873 |
rs547654980 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051547 | GGCAGAGGTAGTAAA[A/C]CAAACAACAATGAAA | 9873 |
rs547657920 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121355 | AGTCCATTATTCCCA[C/T]TCTACACAGATGAAG | 9873 |
rs547662138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856415 | CTCTCCTCTTAACCA[C/T]TGTTTGCCTAATACA | 9873 |
rs547672561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027769 | GCCCAGGACCAGGGC[G/T]GTGCTGCTCTGTGCA | 9873 |
rs547696275 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909912 | GAGGAGCACCTCTGC[C/T]CGGCTGCCCATCATC | 9873 |
rs547715206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129949 | GTGTGATCTCAGCTC[A/G]CTCACTGCAAGCTCT | 9873 |
rs547725094 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865731 | TTCAAAGAATCATGA[C/G]ATTCTGGAGTTGGTG | 9873 |
rs547735822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904311 | CTAAGAGGATCACCT[C/T]TCTAGTTGCCAAACT | 9873 |
rs547769705 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870006 | TGTTTCTTTCCACAC[A/C]CCCCTATGCTCCCAC | 9873 |
rs547776300 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091441 | GTAATCCCAGCTACA[C/T]GGGAGGCTGAGGCAG | 9873 |
rs547777477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079434 | CGAACTCCTGATGTC[A/G]TGATCCGCCCGCTTC | 9873 |
rs547779801 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129306 | CCCAGGCCACGGACC[A/G]CTAACGGTCTGTGGC | 9873 |
rs547787051 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857562 | TCCTGCCTCAGCCTC[C/T]GGAGTAGCTGGGACT | 9873 |
rs547788844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112985 | ATGCCCTTTTGCAGC[A/T]ACTTTCTAGATCTGG | 9873 |
rs547793044 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911263 | CTTTCTCCAATGTAT[C/G/T]TTCTTGACAACTTTG | 9873 |
rs547810415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991099 | CTCTACGCAAATAAA[A/C]TAGAAAATCTAGAAG | 9873 |
rs547814946 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872193 | TTGCAAAAATCTGCT[C/T]ATTCTTTTCATAATT | 9873 |
rs547822299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048605 | ATCTGAAGTAGTTAC[C/T]TGGGGCAAGTTCTTC | 9873 |
rs547822347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041233 | TGATTTCCTTTCTTT[G/T]GATAAATATCCAGTA | 9873 |
rs547828865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114916 | ACAAGTACTCCCTCG[A/G]ACGCCATGGCTGGTG | 9873 |
rs547843586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034143 | GAGGTTTGTTACATA[C/T]GTATACATGTGCCGT | 9873 |
rs547851905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980005 | CCTAAGAAGGCAGGA[A/G]GGGATGAGATATAAT | 9873 |
rs547866977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883761 | CATGGTGAAACCCCA[C/T]CTCTACAAAAAAATA | 9873 |
rs547884777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041954 | TGTTTTTGAGACAGA[C/G]TCTCACTCGTCACCC | 9873 |
rs547891735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113899 | TTCTCTATATTACTA[A/G]GCAGAGATTCTTGTT | 9873 |
rs547919718 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934072 | CATGATCGCGCCACT[A/C]CACTCCAGCCTGGGC | 9873 |
rs547931074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944619 | CAAATTGTCCCTGTT[G/T]GTAGATGACATGATT | 9873 |
rs547948361 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950918 | CGTGACTAATTCTCT[C/G]TAATTCAGTGTGAAC | 9873 |
rs547952731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884483 | ATTAGAAATATATAT[A/G]TATCTGTGTGTATGT | 9873 |
rs547965712 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118750 | CTGAGCCCTTACCAC[A/G]TGTAATGCATTGTTC | 9873 |
rs547965752 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059240 | GGCTGAAGACTTTAC[A/G]TTACACTGTGTGAAC | 9873 |
rs548001939 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926920 | TTATTTAACATAAAA[A/G]AGTGAAAAAAATGGC | 9873 |
rs548003355 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113854 | TTGTAGTGGTACTGC[C/T]TTAGTGGTCTTGGTT | 9873 |
rs548009223 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048635 | CTTACAGTAAGTGCC[A/G]GAAGTACGAAAAAGC | 9873 |
rs548014987 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986268 | AGGTCGGAGTGCAGT[C/G]GCGTGATCTCTGCTC | 9873 |
rs548019605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113750 | TGGGAAAGTTTGTCA[A/G]GTATCTGAAGAAACT | 9873 |
rs548034236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023654 | AGAGACTTCCACAAT[C/T]ATGTTCTAGGTATTT | 9873 |
rs548038848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072581 | AACAGTAAGATTTTA[A/C]AAAGTAATTTACAAA | 9873 |
rs548053186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120655 | AATCATTTCATCTTG[C/G]AAGGCGGAGGCTGCA | 9873 |
rs548061512 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868517 | CCTGCACACGTATCC[A/G]GGAACTTAAAAGTTG | 9873 |
rs548062516 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883710 | GCCAAGGCAGGCAGA[C/T]TGCTTGACCCACGAG | 9873 |
rs548063214 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064866 | TGAGGCAGTAATTAA[C/T]AGCCTACCAACTAAA | 9873 |
rs548063357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972058 | ACCTCAATAAAATTG[A/G]TTTAAAAAGAGTTAA | 9873 |
rs548087861 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918274 | TTTATTAGCTCTATT[A/C]GTTTTTTTAATGGGC | 9873 |
rs548095412 | snp | C/T | 2.39043e-05 | 0.0034571 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015905 | TAAAAAATACATATT[C/T]TTTCTAAAATAAATA | 9873 |
rs548102549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073509 | TACTTTGCATGTGCT[C/T]GAGATAAAATTTTCC | 9873 |
rs548104170 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850516 | CCACCACCACGCCCG[C/G]CTAATTTTTTGTATT | 9873 |
rs548104928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964344 | GCTTAAGATGTCATT[A/G]TAACTCTTCTTTGAT | 9873 |
rs548112813 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083356 | GAGATCGAGACCATC[C/T]CGGCCAACATGGTGA | 9873 |
rs548122420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129153 | TGGGATTACAGGCAT[A/G]AGCCACCGCGCCTGG | 9873 |
rs548123507 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124526 | TTTGGGAGGCCAAGG[C/T]AGGTGGATCACCAGA | 9873 |
rs548129955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900175 | TATACATAACTTTCA[C/T]CCCAACACCAGGTCC | 9873 |
rs548130978 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092933 | GTCTACCTGGGGACC[C/T]TGTGCCACACCAAAT | 9873 |
rs548134043 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844927 | AACCCCACTCATTTA[A/C]CCTTGATAGCTTTTC | 9873 |
rs548144995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956123 | TATCAGTCAAGTATG[G/T]AGCAATTTGAGCGTA | 9873 |
rs548147258 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033555 | TAGGGCGCTACACAA[C/G]ACATCTTCCACAAGA | 9873 |
rs548158733 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016488 | TTGATATGCCTTTCA[C/T]TTTTAACTATTTGAC | 9873 |
rs548174229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908473 | ACTGTTTTCCATAGC[A/G]GTTGTACTAATTTAC | 9873 |
rs548176656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067998 | CAGACACGAGAGAAT[A/G]AGAACCAAGTGAAAG | 9873 |
rs548185018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976683 | GTAACCAAAACAGTA[C/T]GGTACTGGCATAAAA | 9873 |
rs548195704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923008 | CCTCTATGGATTTGC[C/T]TACTCTGGATATTTC | 9873 |
rs548203922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128978 | CCGGGTTCAAGCGAT[C/T]CTCCTGCCTTAGCCT | 9873 |
rs548211131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908944 | CAGGTGTGAGCCATT[G/T]CATGTTGCCCTGTCT | 9873 |
rs548216744 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891048 | CAGCCTCCTGAGTAG[C/G]TGGAACTACAGGTGT | 9873 |
rs548219793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044246 | TGCCTCACTTATTAA[C/T]GCTGAATTCCTCAAT | 9873 |
rs548240268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061190 | GGTGGGGGGTCACCT[C/T]ACCTGGGAAGCACAA | 9873 |
rs548244847 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837531 | TATTGTGCTCCCTAC[A/C]TTCTACAGGAGCGGA | 9873 |
rs548270288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044738 | ACATAGTACATGCAA[C/T]AATTTAACATTCTAG | 9873 |
rs548272593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093253 | CCCTGTACACCTCTT[C/T]CCTTGGCTGATTTTA | 9873 |
rs548275819 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086175 | CACTTTTGAGAGATA[A/G]AGGTGGGTGGATCAC | 9873 |
rs548276498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936933 | GTATGGACTTCCTTG[A/G]AGACAGTTTCTCTTG | 9873 |
rs548277054 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121554 | CTTGGGTTGCTAAGA[G/T]TTAAATGAAATAATA | 9873 |
rs548281094 | in-del | -/TAAAT | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125401 | CTAAGTAGACAGTGA[-/TAAAT]TAAGAATGCATGGTG | 9873 |
rs548297236 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901849 | GTTCATTATTCCATT[G/T]ATTAATTCTATTCTG | 9873 |
rs548298616 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876061 | ACAGTGGCTGACACC[A/T]GTGATCCCCACATTT | 9873 |
rs548306068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084675 | TTGGGATTACTGGCA[A/T]GGGCCAACGTGCTTA | 9873 |
rs548323250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045295 | GAGGATGTGGAGAAA[C/T]AGGAACACTTTTACA | 9873 |
rs548351278 | in-del | -/AAAAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096027 | TATAGAAAAAAACAA[-/AAAAC]AAAACAAAACAAAAA | 9873 |
rs548356077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030922 | ATCTCTATACTTGCG[C/T]GTCCTGAATTTCTGC | 9873 |
rs548369659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062203 | GCAAACTTCAGCAGA[C/T]CTGCAGCAGAGGGGC | 9873 |
rs548387112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930071 | ATGAAAAAAATAATA[C/T]GTTGTGAAAGTTGAT | 9873 |
rs548398323 | snp | A/G | | | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836703 | GGGCCTTTTGGAAAG[A/G]TCTGTTTACCCAAAC | 9873 |
rs548418438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869427 | AAGGGAAAGAGAGGG[C/T]TGGGGGGAGGGAAGA | 9873 |
rs548430279 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076528 | TGATGGTTACTTTGG[G/T]CTCAGGATAAAAGTA | 9873 |
rs548435517 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927965 | TTACTTACTTTATCA[A/T]GTTAATGATTTTCTC | 9873 |
rs548443348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939315 | AAATTGTAACTAAGC[A/G]TTTTTCCCCCAGTCG | 9873 |
rs548460319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001201 | GTTGGCTAACCTTTT[G/T]CTCACAGGGCAGCAC | 9873 |
rs548463172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128126 | GGAGGAGAATCCTAA[A/G]AGGCCAAAATACAAA | 9873 |
rs548473508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094012 | GGTCAGGAGTTCAAG[A/C]CCAGCCTGGCCAACA | 9873 |
rs548479615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946035 | ATTTGACCCAGCCAT[C/T]CCATTACCGAGTATA | 9873 |
rs548491010 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133993 | ATTGTACAATCCTAT[-/A]AAAAAAAAGTTGAAT | 9873 |
rs548502233 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967616 | GAACTAGGGAGTAGG[A/G]AGAACACAAAATGAC | 9873 |
rs548505405 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847103 | CTGGGCTCCAGTGAT[C/T]CTCCTGCCTGAGCCT | 9873 |
rs548537887 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851313 | CAAGGTGTAAGACTA[C/T]GTATTTTAAGATGTT | 9873 |
rs548540521 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959696 | AACGCACCTGCTCCC[A/C]ATAGCTTTCTATGTG | 9873 |
rs548547922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894603 | ATTTCAATAAAGTTA[C/T]TAATTATTTATCCTC | 9873 |
rs548569590 | snp | C/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839139 | ACTAAGATCCTAGCA[C/T]ATCCTCCAAAGCAAA | 9873 |
rs548580255 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061547 | CGGAGCCCAGCAAAC[A/T]AAGATCCACTGGCTT | 9873 |
rs548601877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095876 | ACACTATGAACAGCC[A/C]TGCAGCAGCAATCTT | 9873 |
rs548610416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119300 | AGAGCGAGACTCTGC[C/T]TCAAAAAAAAAAAAA | 9873 |
rs548623052 | in-del | -/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144036 | AGAGCCCAGGCCATA[-/G]GTAGCGTAGGCTGGG | 9873 |
rs548625848 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130744 | TTCTCTGCCTAGTTA[A/G]CATCTCCTTTTTCTC | 9873 |
rs548626109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960186 | CGAAGGCAGAGCAGG[A/C]ATGTCACAAGGGAGC | 9873 |
rs548628649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045049 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 9873 |
rs548632227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853477 | TGGAGTGTAGTGGCG[C/T]AATCTTGACTCACTG | 9873 |
rs548637226 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040295 | AAGCTGTAATTGTTT[C/T]GCAGTCATGTGGAAA | 9873 |
rs548648906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908515 | CAGTATACAAGGGCT[C/T]CCTTTTCTCCACATC | 9873 |
rs548652610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108951 | TCATTCTTCTGCATA[C/T]GGATATTCAGTTTTT | 9873 |
rs548662208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072400 | AATGAAGTTTAAAAA[C/T]TTAATTAAATTTTTA | 9873 |
rs548668632 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909387 | TCTCGGCTCGCTACA[A/G]CCTCCACCTCCCAGC | 9873 |
rs548669638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000518 | ATATAATTAAAGTTT[A/G]GAGTCCATCAGGTTT | 9873 |
rs548676661 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019920 | TTTTTTAAAGTTTTT[A/T]AAAAAATTTTTTTCA | 9873 |
rs548706214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048819 | GGGGAATGAATATTT[C/G]CTGAGCAATAATTCA | 9873 |
rs548707383 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945513 | TCATGTCTAAAACAC[C/G]AAAAGCAATGGCAAC | 9873 |
rs548710358 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903814 | TGGGAAAAGGGATAA[C/T]TGAGGAGACGCAAAA | 9873 |
rs548713481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101741 | TGCACCCCCCGCCCC[C/T]GAAAAAAACACAACA | 9873 |
rs548715335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109605 | TGGTTTTTTAGTGGG[C/G]TCTTTATGTTTCCCC | 9873 |
rs548718362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058187 | CCTGGCCAATTCTGT[A/G]TTCTTTAAAGGTATT | 9873 |
rs548723485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893614 | GCCACTATGCCCAGC[C/G]CAATATTTTTCCTTT | 9873 |
rs548726152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064816 | AACCAGAAAGAAGTC[A/G]AATCCTTGAATAAAC | 9873 |
rs548729084 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906821 | ATGCTGTTTTGGTTA[A/C]TGTAGCCTTGTAGTA | 9873 |
rs548742695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012057 | TACACTTTCAGTGTA[C/T]AAAAATATACTTATG | 9873 |
rs548763299 | in-del | -/C | 0.0185938 | 0.0946107 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009364 | AGCCAGGTGTGGTGG[-/C]CGTACACCTGTAATC | 9873 |
rs548766118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847464 | CACAGACAAGGTAAA[C/T]ATACAGAGACAAAAC | 9873 |
rs548767845 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993417 | TTACTGGGTATATAC[C/T]CAAAGGATTATAAAT | 9873 |
rs548769087 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905302 | CTCTGTGGGTATATA[C/G]TAGGTATTTATATTT | 9873 |
rs548777974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102374 | CAATTACACTCCTAA[A/G]TACTTATCCAAGAGA | 9873 |
rs548784630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112881 | ATGTTAGCCAAGCTC[A/G]TCTTGAACTCCTGAC | 9873 |
rs548801687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094835 | TACTGCAATAGCACT[A/G]AAATGATGACCTGAG | 9873 |
rs548813860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885856 | AAATGACTATTCATT[G/T]TACACCCTGCCCTCC | 9873 |
rs548821112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942432 | TGTAAATGGGCTAAC[A/T]CAGGCAGGAATAGCT | 9873 |
rs548834753 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948791 | CTGCCTCAGTCTCCC[A/G]AGTAGCTGGGACTAC | 9873 |
rs548838430 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039576 | TGTAAGTTTGTCACA[A/G]GTGAATTTTAAAAAT | 9873 |
rs548847090 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868533 | GGAACTTAAAAGTTG[-/A]AAAAAAAATTAGCTA | 9873 |
rs548861592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897252 | GGTATAGTTGTCCTT[C/T]CATATCTGTGGGTTC | 9873 |
rs548864891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087062 | AAAAGGCATTGTATC[A/G]TAGGAGATGACAGCT | 9873 |
rs548883044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986305 | ACCTCTGCCTCCTGG[A/G]TTCATGCCATTCTCC | 9873 |
rs548888457 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844992 | TGCCTTGAATATGCC[-/A]AGCAAAAGGCATTTT | 9873 |
rs548899667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032668 | GAAAGTATATGGGAA[C/T]ATAAAGCAGAGAGAT | 9873 |
rs548909263 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935006 | TCCCTTACACATTAC[C/T]TCTGCCCTCTTTATT | 9873 |
rs548910289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038937 | GTTCTTTTTCCAGTA[C/T]ATTTTTTTGGCTTGA | 9873 |
rs548915910 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064102 | TCTCAGGCCACAGTG[A/C]AATCAAACTAGAACT | 9873 |
rs548939910 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952483 | GCATGTGTCACCACG[C/T]CCAGCTAATTTTTAT | 9873 |
rs548944467 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935939 | AAGTCAGATGTCTGA[A/C]AAAGGTCTGCTGTAC | 9873 |
rs548944535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011395 | ACCTAGGCTAGCAGG[C/T]GGGGAATACTTGCCC | 9873 |
rs548956591 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929460 | CCTTCTGGCCTGGGT[A/G]GATTATTGCTAGTGT | 9873 |
rs548959432 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979556 | GCTTTGGATTCTCAA[C/T]ACTTACACAGTAAAG | 9873 |
rs548964330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132292 | ATAACAGTAGCTACC[A/G]ATGCTAAATACCTAC | 9873 |
rs548973502 | in-del | -/CC | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072993 | TTAAGCAAGGAGCCG[-/CC]CCCTTAAAGTCCACA | 9873 |
rs548977116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972416 | TTCAAGGTGCCCTAG[A/T]ATTCAGCCTGATGCC | 9873 |
rs548992252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989659 | CCAACTCCGTGGATA[A/C]ACATATACATTCGAG | 9873 |
rs548994050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904628 | TTTAAGAAAATATAT[A/C]CATATTACAATTTAC | 9873 |
rs548995394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083506 | GTGAGCCAAGATTGC[A/G]CCACTGTACTCCAGC | 9873 |
rs549001315 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131368 | TAAAAGTACAAAAAA[A/C]AAAAAAAAAAATTAG | 9873 |
rs549025670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139868 | AGGAAAAAGTTTGTA[A/T]TGTGTTAGTTCCAGT | 9873 |
rs549029605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856573 | AAATTATATATTTTT[C/T]CTGACATATTTATTG | 9873 |
rs549059424 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139933 | TTAAAGCAGGAAATC[C/G]AAAAGGAAATTCCAT | 9873 |
rs549063034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138752 | AGCTAGGACTACAGG[C/T]GCACGCCACCATGCC | 9873 |
rs549075748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104623 | ACCCAGGCTGGAGTG[C/T]AGTACCGCAATCTCA | 9873 |
rs549078184 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105121 | TATTCCCATTCCATA[A/C]ATGAGGAAAGTACAA | 9873 |
rs549079776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981350 | AATCTGTGAGCTGGC[C/T]AGGCCCTTTAACTTC | 9873 |
rs549083542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115824 | TAATTGTGAGACATA[C/T]CCACATTATTGAGGG | 9873 |
rs549090482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956568 | TGAGAAATCCAAGAT[C/G]AAGGCGCCAGCAGAT | 9873 |
rs549091095 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849527 | TTCAATGAGGAGCAG[A/G]GGACAACCAACTGAG | 9873 |
rs549094870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857478 | AGTTTCACTCTTGTC[A/G]CCCAGGCTGGAGTGC | 9873 |
rs549101212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003688 | AGACGGGGTTTCACC[A/G]TTTTAGCCGGGATGG | 9873 |
rs549102924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070748 | CAAATTAAAAAAAAA[A/G]AAGAAATTGAACAAG | 9873 |
rs549113684 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102188 | ATACCACTGAACACC[C/G]ACTAGAATGACTAAA | 9873 |
rs549115079 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027979 | CTAGATTTCAGAGAA[A/T]GTATGGAAACACCTG | 9873 |
rs549116689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875198 | TTTACTTGTAGAATA[C/G]AATCAATAATGGTAG | 9873 |
rs549123297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905773 | GGACATGAACTCACC[C/T]CTTTTTATGGCTGCA | 9873 |
rs549124526 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977097 | ACCTGGCTAATTTTT[C/G]TATTTTTAGTAGAGA | 9873 |
rs549126055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138278 | TACAAGTCAGCACAG[A/T]TATCAGGACACAAAC | 9873 |
rs549127097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004616 | ATGTATGCCCTTTTT[A/G]CCCTTGCCTCTTTCT | 9873 |
rs549141327 | snp | C/T | 0.0433635 | 0.140717 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097633 | TTTTTTTTTTTTTTT[C/T]CTAATTACTGATTCA | 9873 |
rs549145077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122871 | ACAAAGAATCTACAA[G/T]ATATGCAGATTAAGT | 9873 |
rs549152619 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074436 | ATCCTCACCCCAATA[C/T]AATATCACATACGAA | 9873 |
rs549161982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042135 | TTTCACTGTGTTGGC[C/T]AGGCTGGTCTTCAAC | 9873 |
rs549178765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105890 | TGTATTTCAGGTCTC[C/T]AATAAATCTGACAAA | 9873 |
rs549187515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966263 | CTCCCGGGTTCATGC[A/G]ATTCTCCTGTCTCAG | 9873 |
rs549189500 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093315 | CCTTACTGAGTAAAC[A/T]TTCAGTGAGCTCTGA | 9873 |
rs549193468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137744 | AAAGACAACAGCATA[C/T]ACAGGGGCATGAATG | 9873 |
rs549204940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897936 | CTTTCTGGTATCATC[A/T]GAGAAATGATAATTG | 9873 |
rs549207005 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988892 | CATGCTCACTACTAA[C/T]AGAGAACAAACTATT | 9873 |
rs549207381 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904798 | TAGTTTCTTCATCTA[G/T]CTCTCCTTTCCTCCC | 9873 |
rs549217934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106816 | AACAACAGACCAGAG[C/T]CTCCATGTGCAGTAG | 9873 |
rs549224325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958673 | TCCACTTTCTCCTTT[C/T]ATTAAAAATCTACCT | 9873 |
rs549225814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997431 | AACATCTTCCCAGAG[C/T]CTCTACAGTTTTTAT | 9873 |
rs549243569 | snp | A/G | 1.64991e-05 | 0.00287215 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843184 | GGCTGCCTGAAACGA[A/G]TTCTGCTTCCGTGGA | 9873 |
rs549244242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889193 | GTCTCGATCTCCTGA[A/C]CTTGTGATCCACCCA | 9873 |
rs549256890 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851658 | TGAGGCAGGAGAATT[G/T]CTTGAACCTGGGAGG | 9873 |
rs549259384 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037589 | CACAATATTCTTGTC[A/G]TCTTTAGATATTCTA | 9873 |
rs549263625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066550 | ACTATCATCAGAGTG[A/G]ACAGGCAACCTACAG | 9873 |
rs549270391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116589 | TCTGCCACCCATGCT[A/G]GAGTGCAGTTGTGTG | 9873 |
rs549271057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998265 | TTAATTTGGACCAGG[C/T]GAGGTGGCTCATGCC | 9873 |
rs549281553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107299 | GTGATCTGCCCAGCT[C/T]GGCCTCCCAAAGTGC | 9873 |
rs549286687 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018361 | TTACTATTTGTGTCT[C/T]TTTCTAAAACGCCTT | 9873 |
rs549292990 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974801 | TCTCTCCAAGAAAGA[A/G]GGCATTAAAAAAAAA | 9873 |
rs549325439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091564 | AAAAAAAAGAAAAAA[G/T]AAAAGAAAGCAAATA | 9873 |
rs549336915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086200 | GATCACTTGAGGCCA[A/G]GAGTTTAAGACAGGC | 9873 |
rs549346185 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084883 | AGTTTAAAGACTTTA[C/T]CGTTATGTGCCAGGA | 9873 |
rs549349834 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036106 | ACTAAAGGCTAAGAG[C/T]AGACTGGCTTGGACA | 9873 |
rs549364413 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139025 | TCTTGATATATCCAG[A/G]TTGGATGAGAATAGA | 9873 |
rs549369053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882152 | CGTCTCAAAAAAAAA[C/G]AGAGCAGAGGCTGGG | 9873 |
rs549370117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950619 | GTTTTAGTACCTTTG[C/T]TGACAATCAGCTACT | 9873 |
rs549370403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982100 | TATTTTCTAACCTGT[A/G]TTCTAATAAGCAGAA | 9873 |
rs549371115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990250 | AGATCTGTGTTTCAA[C/T]AGAAACCTGATGAGA | 9873 |
rs549380023 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861743 | AAGACCAACCTGACC[A/G]ACATAGAGAAACCCT | 9873 |
rs549384770 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073811 | CATAAAATCAAATAA[A/T]AAAAACTGTACATGT | 9873 |
rs549404359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882867 | GGCAATGAGAATAGT[C/T]CAAATAATTCTAAAA | 9873 |
rs549404584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860235 | CATGGACCGGTAAAA[C/G]GTTCGTTCCAGTCTA | 9873 |
rs549409373 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967185 | AGCCTGGGCGACAGA[C/G]CAAGACTCTGTCTCA | 9873 |
rs549416700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844380 | AAGGAAATGATTGAG[A/G]TCAGTCATGGTTTGG | 9873 |
rs549434845 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899322 | CAATCCAATAAAAAA[A/G]TAGAAACAAGGTTTG | 9873 |
rs549442263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977706 | ATGTGAAGAAACAGG[A/G]ACACTTTTACACTGT | 9873 |
rs549442512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968255 | AACAAATGAAAATAA[C/T]TACAGATAAATAACA | 9873 |
rs549449667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029017 | GAAAACGGACTAACA[C/G]AGGAAGCATGACATA | 9873 |
rs549453627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021084 | GGTCTCGCTATGTTG[C/T]CCAGGTTGATCTGAA | 9873 |
rs549466266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919548 | GTCCAATTTCCTCCA[C/T]ATAAAATGAACATGG | 9873 |
rs549470844 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003263 | AACTGGCAAATGGAG[A/T]AATAACAAAAATACC | 9873 |
rs549474438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867767 | ACTAGCAAACTATTA[G/T]CTTTTTAAAAAATTT | 9873 |
rs549487298 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013814 | ACCTGAATCCTGAAT[C/T]TTAAATAAACTTGGA | 9873 |
rs549511801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023195 | AAAAATGATAAATTG[C/G]ACCTTATCAGAATTA | 9873 |
rs549512977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021890 | GCCCAGGCAACACAA[A/G]GAGACCCCTGTCTCT | 9873 |
rs549549271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986228 | TTATTTATTTATTTA[A/G]AGACGGAGTCTCGCT | 9873 |
rs549558305 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865569 | TACTAGGCACAGCTC[C/T]TTCATTCCCTTCCTT | 9873 |
rs549574408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022869 | GTGGAACAAAAGAGA[A/G]ATCCCAGAAATAGAC | 9873 |
rs549576009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931782 | AAACACAAAAAACTC[C/T]TCTTACATCTTGCAT | 9873 |
rs549592705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913024 | AGGGGAAGCAGCTTT[A/G]TCTTACGTGGCAGGA | 9873 |
rs549597815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863006 | TAGTTCGCTGTAACC[C/T]TGAACTTCTGGGTTC | 9873 |
rs549602631 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878922 | GACCAGCCTGGCCAA[C/G]ATGGTGAAACCCCGT | 9873 |
rs549620705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924051 | TGCAAATATTTTCTC[A/C]CATTTTGTGGGCTGT | 9873 |
rs549631301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913565 | TGAGCCATCACACCC[A/G]GCCCTATTTATCCAT | 9873 |
rs549656632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006543 | CACTGTGACTACCCC[A/G]CTTTGAGCCACCCTC | 9873 |
rs549659237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863583 | CAGACTAGAAGAAAA[C/T]TGCATAAATCAAATA | 9873 |
rs549661132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855086 | CGAAACCAGTCTGAC[C/T]AACATGGAGAAACCC | 9873 |
rs549681651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110385 | TGTTATTGCTCTGTT[C/G]AGGTTTTGGATTTCT | 9873 |
rs549695587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951323 | GTAAGCAGTGATGAA[A/G]CAGATGCTGCAGATT | 9873 |
rs549696152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982253 | GAAGGTCCCGAGAAC[G/T]GTCCCATCTCTACTT | 9873 |
rs549717343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907406 | AGAGCATCCTTATCT[C/T]GTGCTGGTTTTCAAA | 9873 |
rs549721036 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909477 | CTAGGAAGTGAGGAG[C/T]GTCTCTGCCTGGCCG | 9873 |
rs549728217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930924 | GTACATTTTAAAATA[C/T]CTTAAGAGTGTAATT | 9873 |
rs549728409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002224 | TAGAAGTAAAGGAAA[A/C]AACTTGATAAACTAT | 9873 |
rs549731850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070887 | CTGGAAGTGAAATAA[C/T]GTGGTCTGAAAACTA | 9873 |
rs549731920 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986141 | TACTTCCCCATTGTT[-/A]AAAAAAATTGGGTTT | 9873 |
rs549753812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138898 | CAGGTGTCAGTGACT[A/G]CGCACGGCCTCGCAT | 9873 |
rs549756497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878387 | AGCTCTAACAACAAA[A/G]AAAAGATAAAAAAGA | 9873 |
rs549771342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885713 | CATCTAGAGTGCGGA[C/G]AAACAAACAACAGGA | 9873 |
rs549780882 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946290 | TCTCAGCAGACTATC[A/G]CAAGGACAAAAAACC | 9873 |
rs549795982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031816 | CACAGCAGCCTTTTC[A/G]CCTGGAAAAGGCATA | 9873 |
rs549809554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010339 | TTTTCAGAATTTTCT[C/T]GTATCTCATTGAGCT | 9873 |
rs549820205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923334 | GGAATGGAATTGCTC[A/G]GTCATATGATAACTC | 9873 |
rs549846535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078807 | CACTGCAGCCTTGAA[A/G]TCCTGGACTCACGTG | 9873 |
rs549857389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032556 | ATTGCTCAGTATTTT[C/T]AAAGCAAATGTTTAT | 9873 |
rs549857656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024567 | ATGAATTACATGGGG[A/G]TAAATTAGAGTCACA | 9873 |
rs549908018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070257 | CTAACAAGCCTCTTA[C/T]ATGGCATAGGCCCTG | 9873 |
rs549912734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915031 | CAGCATCTATAAGGA[A/C]CTTAAACAAGTTTAC | 9873 |
rs549920566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025237 | AGACATGGAATCAAC[C/G]TAAACGCCCATCAGT | 9873 |
rs549924307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017143 | ACATGCCACTGAGCC[C/T]AGCTAACTTTTTGTA | 9873 |
rs549925932 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030874 | AATCCTGAATACAAT[A/G]TTATTAACTATAGTC | 9873 |
rs549931489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879940 | GGAGGCGGAGCTTGA[C/T]GTGAGCCGAGATCGC | 9873 |
rs549950601 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104290 | TTTATTTATGGAGAC[A/C]GAGTCTCACTCTGTT | 9873 |
rs549950812 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961408 | TTTAAGAAGTTTTTT[G/T]TTGTTGTTGTTGTTG | 9873 |
rs549952686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895576 | GCACATAACTAATGC[A/G]TCTATGCAAAGATCT | 9873 |
rs549983991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116420 | AATGAGCTGGGTGTT[C/T]TTCTCATTCTGTGAA | 9873 |
rs549986337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009776 | CTGCTAGTAGTCTCA[C/T]AGCAGTTCCTTGACA | 9873 |
rs549989403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840635 | TCTAAATCACTTTCA[A/T]AGCCATCATCTTGCA | 9873 |
rs550024701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062255 | AACAGAAAGGAATAG[C/T]ATGTGCACTCAAACA | 9873 |
rs550038627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909341 | CTCACTCAATGCTCA[A/T]TGTTGCCCAGGCTGG | 9873 |
rs550041814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953608 | GACATTATTCCAGGT[A/C]CTGGAGACACTGCAT | 9873 |
rs550044829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115697 | GACAAGTCCAAAATC[C/T]GTAGGGCAGGCCATC | 9873 |
rs550058038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847794 | TCCTCCTGAGTTCAA[C/G]TGATTCTCCTGCCTC | 9873 |
rs550064861 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838126 | CCTCCATATTAGCTC[G/T]GCTAATTCTAAATGA | 9873 |
rs550070051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916818 | TCTATGTTTTCTTTC[A/G]TTACTTGTGCTTTCA | 9873 |
rs550072693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902881 | TAGATCAGATTTGGG[A/G]ACTGGACAATATATA | 9873 |
rs550081261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987788 | TGTTCTAGGATCTCT[A/G]AAAGTTTAAGAAAAC | 9873 |
rs550085316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933342 | TAGGAAAGAATTAAA[C/T]CAACTCACAGAGAAA | 9873 |
rs550087716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062908 | ACCTAGCAAGACAGG[C/T]CAATATTCAAATTCA | 9873 |
rs550089321 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082071 | GGCTGGGCGCGGTGG[C/T]TCATGCCTGTAATCC | 9873 |
rs550092834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071418 | TGTCCAGGACTGGGC[A/G]CAGTGGCTCACGCCT | 9873 |
rs550105836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122835 | ACAATAGCTTTATAG[C/T]GTGGCTGTTCTACTA | 9873 |
rs550106820 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865773 | TGGGAATCTCAGAGT[A/C]TTTTAATCTTTCTTT | 9873 |
rs550107126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894802 | AATAAGAGGTTATTT[A/G]TAGTTTTTTCTTTCA | 9873 |
rs550121365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130518 | AAACTATCTTCACCT[A/G]CCTTGGGCTGCAATG | 9873 |
rs550124059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909732 | CCTGGCCGCCACCCC[A/G]TCTGGTAGGTGAGGA | 9873 |
rs550128242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946117 | TTTATTGTGGCACTA[C/T]TCAAAATAGGAAAGA | 9873 |
rs550129689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103428 | AGATTTAATTAGACT[C/T]AGTTTAGGTATCCTC | 9873 |
rs550150395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047071 | ATATAAAAGACAAGA[C/T]GCAGAATAAATGTGA | 9873 |
rs550154234 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095720 | CAACAACAAAAGCAG[A/G]GAACATGGGCTGGCA | 9873 |
rs550168953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121827 | CTGGGCTCCACTCTC[A/T]GAGTTCCTGATGCAG | 9873 |
rs550182757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138156 | TAGATGTGTGCCACA[C/T]CTCATATGTATTGTC | 9873 |
rs550189207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096133 | TAAGAGAAGAAGAAA[C/T]AGAACAGGAAAAACA | 9873 |
rs550200531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873169 | CCCATCTCTACTAAA[A/C]ATACAAAAAATTAGC | 9873 |
rs550202718 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898945 | AGAAAGGGTTTCGCC[A/G]TGTTGCCCAGGCTGG | 9873 |
rs550213607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040617 | TACATAATAATTGTA[C/T]ACATTTAAGGGGCAC | 9873 |
rs550214640 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72844216 | ACGAGAAGGCACTGA[A/C]TTGGAACTGCTACCA | 9873 |
rs550217761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933621 | TGTCTTTTGGTTGCA[C/T]TGTAAGGAAAAAAAG | 9873 |
rs550231972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896364 | TAAGTTTTGTGGACA[C/T]GCATGTTTCCCATAT | 9873 |
rs550239710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890283 | AAAATGTATTCATGC[C/T]AACCTACTATGGTGA | 9873 |
rs550253328 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977500 | TAGGAAAAAAAAATC[A/T]AATAATCTGATTTTT | 9873 |
rs550276611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138633 | TTTTTTTTTGAGACA[A/G]GGTCTCACTCTGTTG | 9873 |
rs550277848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126904 | TTTGCCGAGCATCGT[A/G]TTGCACACCTGTAAT | 9873 |
rs550282039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843610 | ATCATGACAAAAACT[A/G]GGGATCAAAATATTG | 9873 |
rs550292151 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932813 | TCTGTGTTGAGCATA[A/G]GGTTTGGCATACTGG | 9873 |
rs550317500 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141699 | AAGGCAACTCACACG[C/T]GCGCCCCCCACCTGG | 9873 |
rs550324800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978994 | CCCTGAGTAGCTGGG[A/C]CTACAAGTGCATGCC | 9873 |
rs550327474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890945 | TTAATATAGAAAGCA[A/G]CAAAATTGTAGAATG | 9873 |
rs550331048 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045546 | ATGATAGAATGGATT[A/C]AGAAAATGTGGCACA | 9873 |
rs550333086 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004218 | TTACATTTATCATAT[A/C]ATTTAATCCTCATCG | 9873 |
rs550338449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940721 | GCAGAAAACGCCCAG[C/T]TCCTAAGGGTGCAAC | 9873 |
rs550351068 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066684 | GCAAAGGATATGAAC[A/T]GACAGTTCTCAAAAG | 9873 |
rs550352044 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037194 | GAGTTCCCATGTATC[A/T]CTTGCCCCCACACAT | 9873 |
rs550362944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088638 | CACATTCATAAACAT[A/G]TACACACACTTTTTT | 9873 |
rs550368186 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883588 | TAGCCAAATGCAATT[C/T]AAAACCACAGTGAGA | 9873 |
rs550371555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043306 | TAAATCACTAAAAGG[C/T]TCGGTCAAGTAGTGA | 9873 |
rs550384765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73141147 | CGCAGCGGGGAGACT[C/G]ATGACAAGCCGGGTG | 9873 |
rs550385021 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846462 | TGGGATTACAGGCGT[A/G]AGCTACCGTGCCCAG | 9873 |
rs550394575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078235 | TGGAACTCTCATACA[C/T]TGCTGGTGAGAATGT | 9873 |
rs550412259 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099256 | ACTTCCTACCCACTA[A/G]GATGGCTGTAAAACA | 9873 |
rs550458050 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926826 | ACTGAACTTTTGTTG[A/G]TAGTTTTGAATTTAG | 9873 |
rs550477293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030894 | TAACTATAGTCCTCA[C/T]GATACACATTATATC | 9873 |
rs550481058 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873873 | GTAAAACAAAACTGA[A/C]GCTTAACCAATCAAA | 9873 |
rs550487828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928439 | GGAAAATGACATTCA[C/T]TTTCATGTTCCCAAA | 9873 |
rs550488055 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132667 | ATCTCTACAAAAAAA[C/T]ACAAAAATTAGCTGG | 9873 |
rs550496289 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967795 | AATTTTTTTTAAAAA[G/T]AAGTGGGCAGAGAGG | 9873 |
rs550503278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906640 | ATTTAAGCTTTCTAC[A/G]TATAGCTAGCCAGTT | 9873 |
rs550513157 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111409 | TGTCTGATATATGCA[G/T]AGCTACTCCTGTTCT | 9873 |
rs550529441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963516 | CTTCTTTAGCCATTA[C/T]GCTGTGTGTGATTAA | 9873 |
rs550558821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913762 | TTCAACAGTCAAGCC[A/G]AGAGCCAAATTACTA | 9873 |
rs550568010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118731 | TGATGATGGCAAACA[A/C]TAACTGAGCCCTTAC | 9873 |
rs550579142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102333 | AGTTTCTTTTAAATT[A/T]AACACACATTTGTCA | 9873 |
rs550587176 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126074 | CGGCCAGGTGCGGTG[C/G]CTCACACCTGTAATC | 9873 |
rs550595965 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914103 | CGCTGCAAACTGCGC[C/T]TCCTGGGTTCAAGTG | 9873 |
rs550600291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075504 | GCAAACACAATGCAA[A/G]GCAGAAATGCAAAAT | 9873 |
rs550609119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950557 | ATGTGGATATTCAGT[C/T]GTGCCAGTACAATTT | 9873 |
rs550622423 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032590 | CTTCCTAACTGAAAA[A/G]AAAAAAGCACAACAA | 9873 |
rs550646804 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061167 | CCATGGAAGGCGAGC[C/T]GAAGCAGGGTGGGGG | 9873 |
rs550663559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067385 | ACCTAACATAGGTGA[C/T]GGGTTGTTGGGTGCA | 9873 |
rs550669185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117164 | TAACAAATACATTCT[A/G]CATGTACTAACATAT | 9873 |
rs550677449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015123 | TGCTGGGATTACAGG[C/T]GTAAGCCACTGCCCC | 9873 |
rs550680004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044165 | ACCTTTGTATAAATC[A/C]AACAAAGAGACCATT | 9873 |
rs550704957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091796 | TGTAATCCCAGTACT[C/T]TGGGAGGCCGAGGCA | 9873 |
rs550710205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061485 | CCCTGGAAAGGGGTG[C/G]TGAAGCCAGGGAGCC | 9873 |
rs550716143 | in-del | -/ACAG | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065715 | TCCTATACATCAATA[-/ACAG]ACAGAGAAAAATCAT | 9873 |
rs550716631 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987543 | AATAAATGAAGATAA[A/C]GTGGCATTCCTTACT | 9873 |
rs550718318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136260 | GTCTAATGTGCTGTA[A/G]ATTTTTTTTTAACTT | 9873 |
rs550741952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890917 | TTAAAATATAAATTA[C/T]CCAAAGAGGCTTTTA | 9873 |
rs550766553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092289 | TACACCACCACACCC[A/G]GCTAATTTTTTAAGT | 9873 |
rs550767576 | in-del | -/C | 0.0825414 | 0.185628 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082332 | CAGAGTGAGACTTGT[-/C]CCCAAAAAAAAAAAA | 9873 |
rs550771642 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053864 | TTCTTTTTCCCTATG[C/T]ATGACCATTTAAATT | 9873 |
rs550779839 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944892 | ACCACTGCTCAATGA[A/C]ATAAAAAAGGATACA | 9873 |
rs550790410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983120 | TAAAACGGTGAAACC[C/T]CGTCTCTACTAAAAA | 9873 |
rs550791279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852635 | TGCCAGTGCATTGCA[A/G]CCTGGGCAACAGAGC | 9873 |
rs550816570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937640 | GAGCCACCGCGCCTG[C/G]CCAAAATATTTTTTT | 9873 |
rs550816652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945483 | CCATTCAGGACATAG[A/G]CATGGGCAAGGACTT | 9873 |
rs550827205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084653 | CCTGCCTTGGCCTCC[C/G]AAAGCATTGGGATTA | 9873 |
rs550830977 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067755 | AGGCTTTAAACCAAT[-/A]ATTCCAGCAATTGAA | 9873 |
rs550849396 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838286 | GTCTGGGGACTAACC[C/T]TGGGGAGGAGCCAGC | 9873 |
rs550851944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041591 | TAATTTATGGAGTTT[C/T]TTTGTTTGTTTGTTT | 9873 |
rs550871505 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093832 | CTGATCTCGAACTCC[C/T]GACCTCAGGTGATCT | 9873 |
rs550872274 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974749 | AGACAGATTTGAGAA[A/T]CATATGGTATTTATG | 9873 |
rs550878237 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914368 | AACTACCATTGACAT[A/T]CTTTGCAGAACTAGA | 9873 |
rs550888726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085230 | ACTAAGATTTTTTTT[A/T]AAATGTTTATTCAAA | 9873 |
rs550897337 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100433 | CAATGGTGCAATCTC[A/G]GTTCACCGCAACCTC | 9873 |
rs550897647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044852 | GAGGCAGGTGGATCA[C/T]GAGGTCAGGAGATCG | 9873 |
rs550915059 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868337 | GGGGAGAACAACACA[C/T]ACTGGGGCCTGTCAG | 9873 |
rs550918501 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991958 | TTCAATTAGGAAAAG[A/T]GGAAGTCAAATTGTC | 9873 |
rs550920574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071256 | CAAATTCAATTCACG[C/T]GCATACACATGAAAT | 9873 |
rs550931938 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023574 | ACAGAGTACTCCTTC[A/T]ACGGTGGTGGGAATG | 9873 |
rs550943246 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900533 | TGATAAAATAACATC[-/A]AATTAGTCATAATTT | 9873 |
rs550951287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916165 | AAACCCTCCATGACA[C/T]AAGTTTACCTACATA | 9873 |
rs550959945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975628 | TATCACACATACACT[A/G]TAAATATATAGTTAT | 9873 |
rs550973572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846443 | CCTTGGCCCCGCAAC[A/G]TGCTGGGATTACAGG | 9873 |
rs550976279 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898917 | TGTATTATTATTATT[A/T]TTTTTTTTTTAGAGA | 9873 |
rs550977142 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067954 | CTCACAATCATGGCA[G/T]AAGGCTAAAGCCATG | 9873 |
rs550982044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071744 | GTAGATTATTTGAAG[A/G]GAGGGAAATGGACAG | 9873 |
rs550985909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131659 | CAGTAAGCCAAGATC[G/T]CACCACTGCACTCCG | 9873 |
rs550994795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967542 | TGTATGATTCCATTT[A/C]TATGAAATGACCATT | 9873 |
rs551004542 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073988 | CTGATTCTAAAATTT[A/G]TAAGAAAATATAAAG | 9873 |
rs551022538 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961598 | GTTCAGAAATGGATA[A/C]TTTTGAGAAATGAAT | 9873 |
rs551029405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860370 | ACAGTTACCAAGATA[C/T]ACGTTTATACTGGGT | 9873 |
rs551034950 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044170 | TGTATAAATCAAACA[A/G]AGAGACCATTTTAAT | 9873 |
rs551040655 | snp | G/T | 3.36672e-05 | 0.00410274 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838802 | ATCATCACACCAGTG[G/T]GATTTCCACATCTTC | 9873 |
rs551042342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959578 | GTCTACTCTGAGACC[A/G]TCAATTTAGGGTTGC | 9873 |
rs551045657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063883 | TTAAACAGATTAATG[A/G]GACAGAAAATTAACA | 9873 |
rs551046050 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861930 | AAGCGAAACGCCGTC[-/T]CAAAAAAAAAAAAAA | 9873 |
rs551075314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908410 | CCTAGCAGTGAGATT[A/G]CTGAATCATAAGGCA | 9873 |
rs551082311 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107009 | TAAAGCCCACTTCAC[A/G]TCTCTATTATTTTTT | 9873 |
rs551085317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952024 | GGGCATTTTTATTTT[C/T]GGCAAGAATCAAAAA | 9873 |
rs551085906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027122 | GGTAGCAGGCAGAGG[C/T]TGGAACAGTTTGGAG | 9873 |
rs551088241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955061 | TACCAGCTGGACATC[C/T]TCCAGTCCAATTCTG | 9873 |
rs551097134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007758 | ATATGCACACACATA[C/T]ACACAAATGAATGTG | 9873 |
rs551101442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853422 | CACTGGATTTGGCAA[A/T]GATTTTTTTGGAGAC | 9873 |
rs551104942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064709 | AAATACAAACTACCA[C/T]CAGAGAATACTTTAA | 9873 |
rs551112126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900904 | AATACTTTATGAATA[C/T]AATTTGATTTTCCTT | 9873 |
rs551116605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141645 | CTGGGGGTCTCCTGC[C/G]TTAGAGGACGGACGA | 9873 |
rs551126021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124443 | AGAAGAGAGAGAATG[A/G]GGCAGAAAAAAAATA | 9873 |
rs551141869 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874504 | CTCTAGTATTCATTT[C/T]AAAACAATGAAATGT | 9873 |
rs551151159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019035 | TGGGTTACTGCCAAA[C/T]AAGTGGCAAAATGTG | 9873 |
rs551160316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008508 | GACAAGGAAAAAGAC[C/T]GCTTTCAGTCCAGTG | 9873 |
rs551168331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057401 | AAAGCATTCCACCAG[A/G]ATTTCCTTACTGTGG | 9873 |
rs551174287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948056 | TCTGTCACCCAGGCT[A/G]GAGTGCAGTGGTGCG | 9873 |
rs551176790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955779 | TATAGGAACAAAAGA[G/T]TCTCTTAGTGCCCCT | 9873 |
rs551196476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856471 | CAAAATGTCCTTCTG[C/T]ATCCCATAAATATGT | 9873 |
rs551198672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101527 | TCACTGCAGTCTCCA[C/T]CTCCTGGGCTCAAGA | 9873 |
rs551202523 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910219 | GCGCCTCTGCCTGGC[G/T]GCCCATCATCTGGGA | 9873 |
rs551221482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045191 | ATCACTGGCCATCAG[A/G]GAAATGCAAATTAAA | 9873 |
rs551222305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000351 | AATCTCAATTTTTGT[A/G]ACTCTATTTCCAAAA | 9873 |
rs551227157 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964648 | CTTCTGCGTTAACTT[C/G]CGAATCTACCTCTTT | 9873 |
rs551240894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892644 | GAGTCTCACTCTGTT[C/G]GCCAGGCTGGAGTGC | 9873 |
rs551248230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841400 | CCCTTCAGGCGAATA[C/T]GTAGGTTTCTGAAGT | 9873 |
rs551259589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909071 | CCCCCTCCATCTCTC[C/T]GGTCTCCCTCTGTTG | 9873 |
rs551261597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849306 | TGAAGACACACAGAC[A/G]AGGTACACATACACA | 9873 |
rs551265112 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921073 | CTCACTCTCCCTGAC[-/A]AAAAAAAAAAAATTG | 9873 |
rs551268425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992924 | GGATCTAATTAAACT[A/T]AAGAGCTTCTGCACA | 9873 |
rs551270948 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097386 | ATTTTATTTATTTAT[A/T]TTTTTTTTTTGCATC | 9873 |
rs551277654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885024 | AGTATCGATAAAAAC[A/G]AAAAACCACTGCAAA | 9873 |
rs551286565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038845 | CCTGATTCTAAAATA[A/G]AAGTTGAAAAAAAAG | 9873 |
rs551289957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139806 | TAAGACTTTTAAGGT[C/T]CTTGTTTTTTCTGAA | 9873 |
rs551321847 | in-del | -/ATAG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948450 | TAGACAAATATCATA[-/ATAG]ATATTTATTATATCC | 9873 |
rs551330313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089887 | TAGCCATAAAAATTC[C/T]GAGAAAGAGTAATAT | 9873 |
rs551332309 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098239 | CACAGCGTAAGTTTT[A/G]GTATTGTATATTTTT | 9873 |
rs551335665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042220 | ATGCGCCACTGCACC[A/C]GGCTGAGATTATTTT | 9873 |
rs551353852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048653 | AGTACGAAAAAGCTG[C/G]AAATAACTTGCCATG | 9873 |
rs551354341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018396 | AATCACTGTATGCAA[A/C]GTATCTTCGCCTCTG | 9873 |
rs551361546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979711 | CCCATGCCCACTTTC[C/G]CAAGAAGGTACTGGA | 9873 |
rs551362190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962474 | CGTTTGAGAACCTCT[C/G]GTATAAGCGATTGAT | 9873 |
rs551363470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125252 | TTTTTTCCTTCTCTT[A/C]ATCTTTTTAAAAGAT | 9873 |
rs551383828 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038135 | GATTGCTTGAGGCCA[A/G]GAGTTCAAGCCAAGC | 9873 |
rs551396748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996435 | AAATGTGAAAGATAC[A/G]GACAAAAGTATGGTT | 9873 |
rs551401535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980613 | CACAGTCCTCCAGCA[C/G]TAAGTGATTTCCATC | 9873 |
rs551403717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124353 | AATATGGCACATGTA[C/T]ACATATATAACAAAC | 9873 |
rs551404461 | in-del | -/AG | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101620 | TTTTGTATTTTTTGT[-/AG]AGACAGGATCTTACT | 9873 |
rs551410481 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873050 | GTTACAAATCTTAGG[C/T]CAGGCACGGTGGCTC | 9873 |
rs551425033 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941723 | GGTGCAAGGATAGGC[A/C]CTTTCATACACTGCT | 9873 |
rs551430778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863761 | ATTATCAGAGAAATG[A/G]AAATTAAAATGACAA | 9873 |
rs551438572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981207 | AGGAGGGACCAACCC[C/T]TGCCTCTATTTTTAA | 9873 |
rs551448074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73141048 | GCCTCATCCACCCAG[G/T]GCCCAGAGTAGACAT | 9873 |
rs551460965 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055345 | GAGACCCTGTCTCGA[-/A]AAAAAAAAAAAATTC | 9873 |
rs551462151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934196 | TGAGAAGGGCACGTA[C/T]GATGAAGATGCATCT | 9873 |
rs551464559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123729 | CACAGAGGCTGGAGA[A/G]TATATCACCTCTCAG | 9873 |
rs551465891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132147 | CAGCCTAAAAGAGCC[A/G]TAAGATGCATCTTGA | 9873 |
rs551475957 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995333 | CATAAAGAAGTGCTA[A/T]ACATTCTAATAATGC | 9873 |
rs551488452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881627 | AGTGGCCAAGATGTG[A/G]AATCAACCTAAGTGT | 9873 |
rs551489387 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864969 | CTCTGGGATTCCTTT[C/T]TTCCAATCTTACATT | 9873 |
rs551499475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056725 | GAAACAAAAGGTACT[A/T]CAGGAGAGCACATGA | 9873 |
rs551499677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864549 | AGACCATCTCCAAAC[A/C]AACAAAAATACACAT | 9873 |
rs551506563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981986 | GACCCTGTCTCAAAA[A/G]CTATATATACTAAAA | 9873 |
rs551508544 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061178 | GAGCCGAAGCAGGGT[-/G]GGGGGTCACCTCACC | 9873 |
rs551518676 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103040 | GTATGATTCCATTTA[C/T]ATGAAATTCTAGGAA | 9873 |
rs551524100 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011278 | CTGGCAGAATGCTCA[C/G]GTGGGAGGCAGTAGT | 9873 |
rs551524815 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043856 | GAGGCCCTAAAGGAT[C/G]TAGAAATCTCAAGAT | 9873 |
rs551527156 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116649 | GGGCACAAGCTCCCG[C/T]GTCAGCCTCCCAAGT | 9873 |
rs551528767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131485 | AGTGAGCCAAGATAG[C/T]GCCACTGCACTCCAG | 9873 |
rs551549069 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014922 | GATTTCGGCTCAATG[A/C]AACCTCTGCCTCCCA | 9873 |
rs551558016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048058 | ATGAGTTATTTCTAA[A/C]AAGGCAGGAAGTTAA | 9873 |
rs551589206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011866 | TGAATTCCAGTGTTC[C/T]CTTGGATGATCTAGT | 9873 |
rs551590435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905252 | CTGTGCCTGTGTCCC[A/G]CTCTCCTTTTTTTCA | 9873 |
rs551593498 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973867 | ATGGCTGCACTGCAA[C/G]AGCTGAACTGAGTAA | 9873 |
rs551600353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995387 | AAAAGCAGGCTCCAT[G/T]GCTACAATTTTGATA | 9873 |
rs551602568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940998 | TGGGCTGACATCTAC[A/G]GGCCGAAAGAGCCAT | 9873 |
rs551618779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013301 | TTAGAATTTCTTTTA[C/G]CAAACTGTCTGCCTG | 9873 |
rs551638133 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850047 | ATTTTTCATGTTATG[A/G]AAGAATAGAGTTTTT | 9873 |
rs551643095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896619 | TAAGTAGAACAAAAG[C/T]CCCAAGGGACTTTTA | 9873 |
rs551643468 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136484 | GCCCGAGAGGAGAGG[C/T]TGCAGTAAGCAGAGA | 9873 |
rs551657222 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970972 | GGCAGCATTAATGAG[A/G]AACGTGAGATAGCAA | 9873 |
rs551660457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021013 | TCCAGAGTAGCTGGG[A/G]CTGCAGGTGCATGCC | 9873 |
rs551667621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858979 | CAAACTCCTACAACA[C/T]ACTGTATGAAGAAAG | 9873 |
rs551681233 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897123 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCGTCCTG | 9873 |
rs551681522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004834 | TAATCCATTCTTCAC[A/C]CACCCTTCTACACAA | 9873 |
rs551691933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967042 | TCTCTACTAAAAAAA[C/T]ACAAAAAATTAGCCG | 9873 |
rs551723862 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912165 | GACTGCTGTAGCTAG[C/G]ACTTCCAGTACTATG | 9873 |
rs551729443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101282 | CTTTGGGCAAATCAG[A/G]TAAGTGCTAGATTTG | 9873 |
rs551737193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113848 | GAAAACTTGTAGTGG[G/T]ACTGCCTTAGTGGTC | 9873 |
rs551767868 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884031 | ACTAGCACTTGGTAA[C/T]TGCAAAGAGGAAAGA | 9873 |
rs551775128 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956843 | AAAAAAAAAAACCAA[A/C]CCTAGAAGACACCAA | 9873 |
rs551789126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081929 | CATTCAAGATCGGGC[A/G]CGGTGACTCACGCCT | 9873 |
rs551793062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989456 | AGGCAATTCTGTATT[C/T]CCCCATAATCTTAAC | 9873 |
rs551798874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113107 | TTGATAAATTCTGCT[A/G]TTAAGAAATTATGAT | 9873 |
rs551802011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905876 | CAAGTCTTTGCTATT[A/G]TGAATAGTGCCGCAA | 9873 |
rs551815589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934959 | GCCTTTAAGCAGCCA[C/T]GTCCTTTCCAGGTAG | 9873 |
rs551833617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976157 | AGAGTTTAAAGAAAT[A/C]TGCCTAATAATATAC | 9873 |
rs551844220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882102 | GTGAGCCGAAATCGC[A/G]CCACTGCACTCCAGC | 9873 |
rs551845687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877571 | CTATTACAAGAAGCA[A/G]AAAGTCTCTTAGAGA | 9873 |
rs551853463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035308 | TCAAGAGAGTAGCTG[G/T]CACTACAGGCACGCA | 9873 |
rs551869333 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034935 | AAAAAGGTCACTCCA[A/C]AGGCAGCTAAAGTAC | 9873 |
rs551879454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875056 | TTTAACATAAACACA[C/T]ATAAGTGTAAAGCTA | 9873 |
rs551890980 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117325 | AATTCACAATCAGGC[A/T]ATCTGGTTCAAGAGT | 9873 |
rs551892714 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997112 | TAACAGATGACTTCT[-/A]AAAAGCAGGTGTTGG | 9873 |
rs551915453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917673 | GGCGGATCACTTGAC[A/G]TCAGGAGTTCAAGAC | 9873 |
rs551918013 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992800 | GACCTAAAACCATAA[A/C]AACCCTAGAAGAAAA | 9873 |
rs551921054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976777 | AACTCATTTTCAACA[A/G]TGGTGCTAAGAACAT | 9873 |
rs551921330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028368 | TAACTGCCCTGTTAC[A/G]TTTCAGACTTGCATG | 9873 |
rs551921979 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085387 | CATTTTGGAACTAGG[A/G]GTCAACTGAAAGAGA | 9873 |
rs551953059 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102463 | CAGCATTATTTATAA[C/T]AGCCAAAAACTGAAA | 9873 |
rs551956828 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031001 | CACACACACATTGAC[A/G]CACACCTCCAGAAAT | 9873 |
rs551958597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938320 | CCAAGATTTATACTT[C/G]AATTTAATGTCAGCC | 9873 |
rs551961444 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896028 | GGGAAATTTTTGCCA[A/C]ATATTTTTTTAATAG | 9873 |
rs551969629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074453 | ATATCACATACGAAA[A/G]TTTACTTCAGAAAGA | 9873 |
rs551974811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885559 | GATGGCGGGAGGTTT[C/T]GTGGAGTTAGGGTAC | 9873 |
rs551981479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138764 | AGGCGCACGCCACCA[C/T]GCCTGGTTAATTTTT | 9873 |
rs551997748 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139651 | GGGTTGACTGGCTCA[-/C]CCCCAGATATTAACC | 9873 |
rs552012039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878248 | TGTGCCTGTGAATAG[C/T]CACTGCATTCTAGCC | 9873 |
rs552014767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016712 | TCCATATTATTAATT[C/T]TCAAGACAGATTTTA | 9873 |
rs552039255 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852657 | CAACAGAGCAAGATT[C/G]TCTTAAAAAAAAAAA | 9873 |
rs552044913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965561 | AAAACTCAATATTTT[A/C]ATGTATTTATTTCTG | 9873 |
rs552053555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862238 | TCTGTTGACTCTCAC[C/T]ACTTCTATTCAGCAA | 9873 |
rs552075437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014234 | ACTCCTGGGCTCAAG[C/G]GATCGTCCTGCCTTA | 9873 |
rs552077555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957733 | ATAAATTCTGGAGTA[C/T]TGAGAGGTGAGGAGG | 9873 |
rs552084988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066442 | CATAGGCATGGGCAA[A/G]GACTTCATGTCTAAA | 9873 |
rs552086914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058405 | CTAGATGTCATCACA[A/G]TTTGCCCATCAATTA | 9873 |
rs552100155 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887085 | TCTGAAAATATATAT[A/G]TATATATGAATATAT | 9873 |
rs552102071 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850746 | TTCACTGTTAAGTAC[C/T]GACTGACAAGGGCCT | 9873 |
rs552121237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991784 | TAAGAACTATCTATG[A/G]CAAACTCACAGCCAA | 9873 |
rs552129654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949566 | TGCCTGGCAACCACT[A/C]ATCTACTTTCTACAT | 9873 |
rs552130394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062625 | TGAAATACACAGCAC[A/G]AGAACTTCATGAAGC | 9873 |
rs552137553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937561 | TCTGATCTCTAGATG[C/T]TTCCATCTCCTGACC | 9873 |
rs552139056 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009634 | GGAAAGAATTTACTT[C/T]TCCTTCATTTATGAA | 9873 |
rs552153744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884767 | CCCAGCTAATTTATT[C/T]TCATTTGTAACAGAG | 9873 |
rs552160142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919137 | AATAAAAAAAATCTA[A/G]AAAGTGTCAAACTTC | 9873 |
rs552160250 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131599 | ATCCCAGCTACTCGG[A/G]AGGCTGAGGCACAAG | 9873 |
rs552160511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997846 | GCTGGGACTGCAGGC[A/G]TGAACCACCACACCT | 9873 |
rs552164773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892557 | CTATCAAAGATCAAT[A/G]TAAATCAGGATCTAG | 9873 |
rs552185602 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877627 | ATTATAAAGAAATCT[A/G]AAACTTTCAATAGTT | 9873 |
rs552202053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915645 | CCAACAAGGCAAAAC[C/T]CCAGCTCTACAAAAA | 9873 |
rs552211340 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045154 | TTTATGCAGCCAAAA[A/G]ACACATGAAAAAATG | 9873 |
rs552216337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961307 | TAGCTCACTATAGCC[A/T]CGAACTCCTGGGCTC | 9873 |
rs552240482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909284 | TCGAGTGATCTGCCC[A/G]CCTCGGCCTCCTGAG | 9873 |
rs552266600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930196 | GTAATTCTCTGCAAG[A/C]CCGCTGCTGAAACTG | 9873 |
rs552272111 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124013 | CATATGGCAACCCAA[A/C]TGTCCATCAATGATA | 9873 |
rs552273010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038656 | AACATTGAATACAAA[C/T]GGACATAAACATGGG | 9873 |
rs552280569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031640 | GTATCCTATTAGAAT[A/C]TGACCAACAAAGGAC | 9873 |
rs552283956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039864 | AATTTATAGAATAAC[A/G]AATGCAAATCATTTT | 9873 |
rs552289497 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112880 | CATGTTAGCCAAGCT[C/T]GTCTTGAACTCCTGA | 9873 |
rs552307637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077558 | AATGAAACCACTTAT[C/T]CATACACAAATGTTT | 9873 |
rs552311424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930853 | ATGGGTACAAAAAAA[C/T]AGAATAAGACCTACT | 9873 |
rs552314835 | in-del | -/GTG | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962915 | TGACAGTATTACACA[-/GTG]GTGGTTAAGAGAAGG | 9873 |
rs552316608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895530 | CTATAATCACAAGCT[A/T]GATAGGGGAACTTTC | 9873 |
rs552328278 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065500 | TAGTATTGGAAGTTC[C/T]GGCCAGAGCAATCAA | 9873 |
rs552332693 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088883 | TATTTAAATTATGTA[G/T]TTTTTACCCTTTTAA | 9873 |
rs552337370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933260 | AGGCTGAAAGATTAA[C/T]CCAAAAATGGCCTAT | 9873 |
rs552344261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024379 | CGACTAAAGACAAAA[A/C]ACTGTATATAAACAT | 9873 |
rs552371487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055341 | GAGTGAGACCCTGTC[G/T]CGAAAAAAAAAAAAA | 9873 |
rs552375481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847597 | AAAGGACATTTTTGT[G/T]TCCAAAACTTTTCTA | 9873 |
rs552376358 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970527 | AATTCTTTCCTCAAG[C/G]TCAAATTTTTTTCAA | 9873 |
rs552422352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069116 | AGGAGTTTGAGACCA[A/G]TCTGGCCAAAATGGT | 9873 |
rs552434999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046919 | TAAATCAATAGGATG[C/T]AGATCAAAATATGTG | 9873 |
rs552443561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135012 | GTGTGCGCCACCATG[A/C]ACACCTAATTTTTGT | 9873 |
rs552454745 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943709 | TCACTGAGGCACTCA[-/G]AATGATACCTCACAC | 9873 |
rs552482245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940119 | TCAGGTCTAATTCCA[C/T]AGAAGCAGGACAAAT | 9873 |
rs552485194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033871 | CTGTATTTACCTATT[C/T]GATGACGTGACTTGA | 9873 |
rs552496403 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143123 | AAACGGCGGCACTCT[A/G]CTGCAGGGCATTCAA | 9873 |
rs552504467 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096435 | GGGCGCCTGTAATTC[C/T]AGCTACCGGTAAGGC | 9873 |
rs552526733 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952915 | GATAGAATTATCTGC[G/T]TTTCCTCAAGGTCAG | 9873 |
rs552544982 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897915 | TTTTTCTAGAAAGAG[C/T]TCTGGCTTTCTGGTA | 9873 |
rs552550708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062225 | CAGAGGGGCCTGTCA[C/G]AAGGAAAACTAACAA | 9873 |
rs552565207 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142203 | GGGTCTCAGCCGGCC[A/G]GGCGGCGGGTTAGCC | 9873 |
rs552569019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049077 | TAAAAAGTCCTGCCA[C/T]GGGTTCAGCGTAGGA | 9873 |
rs552583954 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052044 | AGGAACTGGTTAATG[A/G]CATGGAAGACCAATT | 9873 |
rs552612182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933734 | ATCTCAAAGCTTAAA[G/T]TAGACAATTTTTATG | 9873 |
rs552625457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846323 | GTAGCTGGGATTACA[C/G]GTGCACACCACCATG | 9873 |
rs552632603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042187 | CCACCTCAGCCTCCC[A/C]GTGTTGGGACTACAG | 9873 |
rs552646398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086322 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGAG | 9873 |
rs552656070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946060 | AGTATATACTCAAAG[G/T]ATTATAAATCATGCT | 9873 |
rs552677918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995568 | AATCAGCCAGGTGTG[A/G]TGGCAAGCACCTGTA | 9873 |
rs552679966 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030799 | ATCCATCATTTCACA[C/T]TGTTATCCCTTTTTG | 9873 |
rs552688952 | in-del | -/TA | 0.00037779 | 0.0137387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843359 | GTGACAAAACAAGTT[-/TA]CACACACAATTTAGA | 9873 |
rs552689086 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880404 | TGTCACAAATACAGA[C/G]ACACAGACCAATGGA | 9873 |
rs552698124 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934354 | TTTTTTTTTTGAGAC[A/G]GAGTCTTACTCTGTT | 9873 |
rs552713783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932020 | CCTCTTAGACTGAAT[C/T]ATTCTCTTTTCCATC | 9873 |
rs552717171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979110 | TGATCTGCCCACCTC[A/G]GCCTCCCAAGGTGCT | 9873 |
rs552726736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927142 | AAAAAACCCTGTAAG[C/T]CTTTAAGGGTAAGGA | 9873 |
rs552728610 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962941 | GAAGGCACACTGGAG[C/T]CAGACTGGTTGAGTT | 9873 |
rs552734470 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952059 | CTGAAGCTTCATGGT[A/G]GGTCTGCATATGTCT | 9873 |
rs552740804 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879023 | GCTGAGGCAGGGGAA[A/C]TGCTTGAACCCAGGA | 9873 |
rs552752243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946694 | ATGGTATAAACAGAG[C/T]AATAGCTACCATTTA | 9873 |
rs552752346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877034 | TGCAGTGCAGTGGTA[C/T]GATCACGGCTCAGTG | 9873 |
rs552756529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986360 | GACTACAGGCGCCTG[A/C]CACCACGCCCAGCTA | 9873 |
rs552768830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840568 | ATTAAATGCTTACTG[A/C]AAAAAGTGTTTCACA | 9873 |
rs552773883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087798 | TATACATTAGTTTCC[C/T]AGGCCTTTACATTCA | 9873 |
rs552776834 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951919 | AAATCCTATTTGACA[A/G]GAATACTGTAACAGC | 9873 |
rs552778655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096005 | AACATCTAATATCCT[A/G]AAGTGCTATAGAAAA | 9873 |
rs552781591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072912 | AAATAGCAAAAAATT[C/T]TAGGTGCAACAGTAT | 9873 |
rs552782931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119270 | ATCATGCCATTGCAT[A/T]CCAGCCTGCACAACA | 9873 |
rs552799415 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990458 | ACATAGTTGGAAGTA[A/C]AGCACTCCTCAGCAA | 9873 |
rs552813843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927675 | TTGCCACTGGCCTGG[C/G]ACCATACTTTGAAAA | 9873 |
rs552821379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848189 | ATCTAAGGATCTTCC[A/T]AGCCAGGATAAAAAC | 9873 |
rs552829078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079762 | ATTAAAGAGTAAGAA[A/G]AACTCAGAAGGATCA | 9873 |
rs552840851 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133716 | CAGAATTGCATGAAC[A/C]CAGGAGGCGGAGGTT | 9873 |
rs552844877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073905 | ATATCAGTTCCCCCT[A/C]AATTGACTTAAAGAT | 9873 |
rs552862630 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986645 | TTCTCCTTTTTTTAC[A/G]GTCATTACCCAAATA | 9873 |
rs552866030 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081995 | ATCACCTAAGGTCAG[C/G]AGTTCGAGACCAGCC | 9873 |
rs552876093 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048082 | AAGTTAAAAAAAAAA[C/T]ACAGGAGGAACAAGA | 9873 |
rs552903485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088585 | GTGTTTTAGTAAACA[C/T]ATAATGTTTGAAAAA | 9873 |
rs552904458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132900 | ATATTTGCAAATCAT[A/G]TATGTTATAAAGAAC | 9873 |
rs552910164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112304 | TTGGCACTTTAAACA[C/T]GTCATGTCACTCTTT | 9873 |
rs552924123 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024822 | AATCCCATTAAGAAA[C/T]GGGCAAAGGACATGA | 9873 |
rs552925540 | in-del | -/TTCT | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901024 | AAATTAGCATTTTTG[-/TTCT]TTTTTAAAAATTTAA | 9873 |
rs552932020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872128 | ATATACGTCTTTATA[C/T]AAGACAATTGGAATT | 9873 |
rs552951628 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957045 | TTTCTTCTTTTTTTT[A/C/T]ATTATACTTTAAGTT | 9873 |
rs552955200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948956 | AGGCATGAGCCACAG[A/C]ACCCAGCATAATTTT | 9873 |
rs552957965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917916 | AAAAAAATTGAGGAC[C/T]GGCTTTTCCATTTCT | 9873 |
rs552969922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066655 | ACAAGAAAAAAAAAA[A/C]CATCAAAAAGTAGGC | 9873 |
rs552989438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105377 | TTCCACTGTCTACAG[C/T]ACACCCTCTATATAA | 9873 |
rs552991370 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096875 | TCCTAGTTTTCTGAG[C/T]CTTTTTATCATGAAA | 9873 |
rs552995729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941868 | AAGGAAGTTATCAAA[C/G]AGGTGTATTAAGATT | 9873 |
rs553008216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889256 | GTGAGCCACCGCGCC[C/T]GGCTATAATTATGTC | 9873 |
rs553015169 | in-del | -/AAAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993067 | AAATTTACAAGAAAA[-/AAAC]AAACAACCCCATCAA | 9873 |
rs553039331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949787 | CTAGTTGATGGACAT[C/T]TGGGTTGTTTCCACC | 9873 |
rs553041254 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958121 | TTCATTTCACATGAA[A/C]ACCTCAGCAATAAGT | 9873 |
rs553050739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097688 | TTCTATTTTTTTCTG[C/T]AATCAGTTTTAGTAA | 9873 |
rs553052709 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060287 | ATTGAAGCATTATTC[A/G]TATCTTCATTTCTAC | 9873 |
rs553060071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843763 | AATCCTCAAGAGGCA[A/G]TGACGTTCAATGAAC | 9873 |
rs553061287 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884492 | ATATATATATCTGTG[C/T]GTATGTTATATATAT | 9873 |
rs553073926 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106899 | GAAATTACCTAATGA[C/T]GCATTTCTCAGAATA | 9873 |
rs553076874 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851361 | TAGTGACAAACGCCT[C/T]GACACAATCTATATG | 9873 |
rs553093577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842534 | GTAAGGCAGAGACTG[C/T]AGCCCACTTTTGTGT | 9873 |
rs553096004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881753 | TGGAACTGGAGGTCA[C/T]TATGTTAAGTGAAAT | 9873 |
rs553098045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118268 | AGACTGCGGTGAGCC[A/G]AGACTGTGCCACTGC | 9873 |
rs553104338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090947 | CTTCTCCTCCCCTGT[C/T]AACTACTAATCTAAT | 9873 |
rs553113296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058740 | ACCTGGCTAATTTTT[G/T]AATTTTTAGTCGAGA | 9873 |
rs553115973 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093858 | GATCTGCCCACCTCG[A/G]CCTCCCAAAGTGTTG | 9873 |
rs553116041 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057599 | TTCTACCTCCTTCTA[C/G]GTGGCCATCAGGACT | 9873 |
rs553139178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035405 | ACTCCTAAGCTCAAG[A/C]AATCCACCCACCTTT | 9873 |
rs553142636 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104613 | TCGCTCTGTCACCCA[A/G]GCTGGAGTGCAGTAC | 9873 |
rs553152401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005229 | TCTTTTATAGAAAAA[A/C]TCCTTGAAAGAATTG | 9873 |
rs553159192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980855 | CTTCCCAAAGCCTAA[C/T]TCAGTAGTTAGCATG | 9873 |
rs553167696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082890 | TATACAACCATAAAA[A/T]GATACATCAACATAA | 9873 |
rs553178414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844446 | AGCTGATCCATTTGC[A/G]TGCTACCGTACAAGC | 9873 |
rs553179311 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099343 | TAGAACCCTCATGCA[C/T]TGCTGGTGAGAACAT | 9873 |
rs553192291 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996344 | CTATAATGGATATGG[C/T]AGCAGTTTGCAAACT | 9873 |
rs553198852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099718 | TGCACCCTCGGTCTG[G/T]TTGGGGCTGTCAAGC | 9873 |
rs553213657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997763 | TGGAGTGCAGTGGCA[C/T]GATCTCGACTTCCTG | 9873 |
rs553217623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943090 | TCCGCCTCCCGGGTT[C/G]AAGTGATTCTCCTTC | 9873 |
rs553237440 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866185 | CAACAGTCTGAAGTA[A/G]ATGAGCATTATGACT | 9873 |
rs553241964 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836716 | AGGTCTGTTTACCCA[A/C]ACCTTTCTATATTAA | 9873 |
rs553247110 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981565 | AATAGTAGACATATA[C/T]AGAATATAGTGAATT | 9873 |
rs553255569 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033140 | AAAAATATAAAAAAT[C/T]AGCTGGGCATGGTGG | 9873 |
rs553260250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991247 | CCAAAAACAGTCCAG[A/G]ACCAGATGGATTCAC | 9873 |
rs553264153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092549 | TTAGTATTTATATGT[C/T]TGGCACAGTGACTGA | 9873 |
rs553268346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982735 | CAGAGGACAGACATC[G/T]TCATATAGCTACTGA | 9873 |
rs553277635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020392 | TAAATTTTACTAAGG[G/T]TTTGCCATTAGATGG | 9873 |
rs553293642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875224 | GGTAGATAATAGTAT[G/T]TGCTACTCCATCTTT | 9873 |
rs553298311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965233 | CTGTACATTATACTG[C/T]AGAAATATTGAACTA | 9873 |
rs553303785 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930441 | TAGAGATTCATCTCT[A/G]TATTTTCTTTGACTT | 9873 |
rs553308765 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987054 | TCCAAACATATTCAC[A/C]CCAGTGTTTCCCAGG | 9873 |
rs553317597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069534 | ATGGATAAGATAAAA[C/T]CCTCAAATAGACACA | 9873 |
rs553320727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912391 | GCTTTTTCAGTATCA[A/G]TTGAAATGATCATAT | 9873 |
rs553329952 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126183 | CATCTCTACTAAAAA[A/T]ACAAAAATTAGCCAG | 9873 |
rs553330081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117406 | TTCCATCCTATTAGG[C/T]TTTTAGGCATATTTT | 9873 |
rs553340210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091961 | AATTGTTTGTACCGG[G/T]GAGACAGAGGTTGCA | 9873 |
rs553368147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858570 | GAAGCTAAATGATTA[C/G]AACATGGACACATAG | 9873 |
rs553383134 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949156 | ATTTTTATCACCACA[A/G]AAAGAAACCTGGCCG | 9873 |
rs553389124 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114326 | GGACTAACCCTTCAG[C/T]GCAGTAGGCTCCCAT | 9873 |
rs553402407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084130 | AATGTTGGCTACTGT[C/T]ATAAGAATAGCTACT | 9873 |
rs553407327 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942856 | GTATGATCATAGTTC[A/G]CAGCTTCAAACTCTT | 9873 |
rs553407536 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140781 | TCCACTTCAAACAGC[-/G]GAGAACAGCAAATGC | 9873 |
rs553414789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059460 | ACTTCAAAGAGTTCA[C/T]AAATCATAAACATAA | 9873 |
rs553431131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851222 | AAAACAACCTGTTCA[A/C]TGAAATTAAAAACTA | 9873 |
rs553435137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029396 | TGTGGACTTGCAACT[A/C]CCAGAGAAAGATTTG | 9873 |
rs553455870 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006084 | GGCTATTTTTTTTTT[A/T]AAATAAAAATAGTAT | 9873 |
rs553461272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968537 | CATGTATCTTAATGG[A/G]GAGCCCTGAAGAGGA | 9873 |
rs553464441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847000 | AATTTAAATTTTTTT[A/T]AAATTTATTTTTTAG | 9873 |
rs553474931 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102127 | TGGTAACAGTGAAAA[G/T]ATGCTTAACATCACT | 9873 |
rs553481779 | in-del | -/ATA | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908591 | CTGAACTAGGATGAT[-/ATA]ATATCTTACTGTAGT | 9873 |
rs553488428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051600 | CAACGACTTTATACT[A/G]TTTTACACAAAAGTA | 9873 |
rs553504403 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137082 | GTGAATTTTTAAAAA[A/G]TCATTCCACTTACTA | 9873 |
rs553515271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998330 | AGATCACTTGAGGTC[A/C]GGAGTTCAGGACCAG | 9873 |
rs553515442 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052506 | CAGTGTATTAGAGAG[C/T]ACTCTCTTCACTGAG | 9873 |
rs553515748 | in-del | -/TGGGGTATAGAGCTTTTT | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967638 | CAAAATGACAGCCAA[-/TGGGGTATAGAGCTTTTT]TGGGGGATAACAGAA | 9873 |
rs553522228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898621 | CATCCCACTTTCATC[A/C]TCAAGTCTACTTGCT | 9873 |
rs553538137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102766 | TCCTCACCAGATGCT[A/G]GTGCCTTGATTTTGG | 9873 |
rs553552240 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064776 | AATGGATAAATTCCT[C/T]GACACATACACCCTC | 9873 |
rs553554192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943556 | AGGGAAGGAAATTGA[A/G]GAGAATGACAGGTGA | 9873 |
rs553570206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890639 | ATAGCTAACTTCTAT[C/T]GTGCAAGGTACTATG | 9873 |
rs553576844 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086739 | TATAGAAGTAAAAAG[A/G]CTGTACAGAGTATTA | 9873 |
rs553577016 | in-del | -/AT | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050378 | GACGTATTTAGATTG[-/AT]ATAGAGACATATCAT | 9873 |
rs553577068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847850 | GGCGCCCGCCACCAC[A/G]CCCAGCTAATTTTTG | 9873 |
rs553577884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062503 | CTCCAAGCTAAAGGA[A/G]CATGTTCTAACCCAA | 9873 |
rs553579402 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091599 | TTCCAGACAGAATTA[C/T]AGAATGTCAAACCAC | 9873 |
rs553592776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936463 | TTGCCTGGGAATTAT[A/C]AGTGTGATTTTATCA | 9873 |
rs553595364 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994287 | GTCTGAATGCTTATT[A/G]CTTCTAAAAAGACCC | 9873 |
rs553599387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103645 | AACTAAAATGAACCT[A/C]TGTAAAACCTACACA | 9873 |
rs553606079 | in-del | -/A/AAA | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968090 | GCAAGACTCTGTCTC[-/A/AAA]AAAAAAAAAAAAAAA | 9873 |
rs553612932 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948198 | TTTTTAGTAGAGATG[C/G]GGTTTTGCCATGTTG | 9873 |
rs553614222 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107638 | CTTCCTTCTACTCTC[A/G]AGTTCCATGAGTTCA | 9873 |
rs553631233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116848 | GGCCCATATCTCTTT[C/T]TTTAGTTATGAACTC | 9873 |
rs553636129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948697 | TTGAGAGGCAGTCTC[A/G]CTCTGTCGCCCAGGC | 9873 |
rs553640436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054983 | GGTAGTTTATAAAAA[C/G]AGGTTTAATGGACTG | 9873 |
rs553646655 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006770 | CTTCCCTCATTAGAA[C/T]GTAGGCTCCATGCAG | 9873 |
rs553669344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986498 | ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCCCAAT | 9873 |
rs553677978 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923880 | GGAGGTGGAGGTTGC[A/G]GTAAGCCGAGTTTGT | 9873 |
rs553682474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137775 | TAGAGTGCACAGTTA[C/G]ACAACCTGACGTCCC | 9873 |
rs553684730 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044304 | AGTCAGAGGCTGAGT[A/G]TGGTGTCTTATATCT | 9873 |
rs553685033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036565 | ATACTGCAAGTCCCT[C/G]ATAAATTATAATCAT | 9873 |
rs553704556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861767 | AAACCCTATCTCTAC[C/T]AAAAAAATATAAAAT | 9873 |
rs553709622 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946246 | TTCATGTCCTTTGTA[A/G]GGACATGGATGAAGC | 9873 |
rs553711157 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848692 | TAACGCAGGGATGTG[-/C]CCTGGGATATGCCAA | 9873 |
rs553719572 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952776 | TGTGCCAGGCACTTA[C/T]ACATATTTACAATTC | 9873 |
rs553721111 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870985 | ACTAACAGTAATGTC[A/T]TTGCTTTTAAACTAC | 9873 |
rs553723946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894949 | ACTTTTCTAAAATCT[A/G]GAAAATTCTGAATTT | 9873 |
rs553740176 | in-del | -/ATC | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085397 | TAGGAGTCAACTGAA[-/ATC]AGAGAGGGGATGACC | 9873 |
rs553740180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928610 | TAGCTCTTCCTTAGC[A/G]TTTTCACAATATTCT | 9873 |
rs553747964 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037386 | ATCATTACAGTATCA[C/T]AGGGAGTTATTTTCA | 9873 |
rs553751162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879962 | CGAGATCGCGCCATC[A/G]CATTCCAGCCTGGGC | 9873 |
rs553759669 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020851 | TTTTATTTAAATTAA[A/G]TATATATAAGAAATA | 9873 |
rs553776653 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892035 | AAGATTGAAGATATA[C/T]TGAAAGATTAAGGCA | 9873 |
rs553785647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113538 | CACGCCCAGCTAGTT[C/T]CTCTATTTTTAGTAG | 9873 |
rs553790360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009126 | AAATGCTGCATGTAT[C/T]ATCAGATAGGCAAAC | 9873 |
rs553814604 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866142 | CCAAATCAAGTGGGC[A/C]TGGAATTTGCTGTCA | 9873 |
rs553821059 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917308 | TCTTTTGCATGTGGC[G/T]ATCCAGCTGTCCCAA | 9873 |
rs553823253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054370 | CATTCCAACACGCAG[A/G]CAGGGGGCTAGAAAA | 9873 |
rs553831218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953210 | GAGAAATGGTCTTGA[C/G]AAAGCATGACAAGCA | 9873 |
rs553833981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909138 | CTGCCTTGGGCTCCC[A/G]TGATTCTCCTGCCTT | 9873 |
rs553842453 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961738 | TGTCATTTTTGTTTA[C/T]AGTTAATCACATGTC | 9873 |
rs553847569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855227 | GCTGTGAGCTGAGAT[C/T]GTGCCATTGTACTCC | 9873 |
rs553848617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120178 | CAACACGTGGGAATT[A/T]TGGGAATTCAGGATG | 9873 |
rs553851737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000837 | AACATAGTACTTAAT[A/G]AGAACATGTTGAAAT | 9873 |
rs553853057 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088188 | TTTTTTAATCTTTCA[A/T]ACCATATTTTTGTTG | 9873 |
rs553870165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945767 | TCTCAAAAGAAGACA[C/T]TTATGCAGCCAAACG | 9873 |
rs553876170 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863013 | CTGTAACCTTGAACT[C/T]CTGGGTTCAAGATAC | 9873 |
rs553884637 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893974 | AAGGCATAGAAGGCT[C/T]AGATATCTGAGCAGA | 9873 |
rs553896429 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019599 | CATGAAATAGACAAA[A/C]AATGAGATCTTTAGA | 9873 |
rs553921920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902213 | TGATTTCTGTGGAGG[A/G]GTACAACATAAAAAA | 9873 |
rs553939494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019329 | ATCACCACAGAGAAA[C/T]TGGACATTAAAAGCA | 9873 |
rs553941149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010656 | CTTTGGCTATGAACA[A/G]TGTCAGTGGTGTTTG | 9873 |
rs553962963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902940 | TTACACAAAAAGCTA[C/T]TCTGTGTAACACAGA | 9873 |
rs553968688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045669 | AAACTATCGCAAGAA[C/T]AAAAAACCAAACACC | 9873 |
rs553973672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114009 | GCTGGGCCTCTGTCC[C/T]TCCCTTTAGGGTGGC | 9873 |
rs554030195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046324 | AAAGCCTTATGAACT[G/T]ATTTTAAAAAGAAAA | 9873 |
rs554045325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087512 | GGAGTTTGAGACCAG[C/T]CTGCCAACATGGTGA | 9873 |
rs554048231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864126 | TACAACAGAGTAGAC[C/T]GGCAGTTTGCCCTTG | 9873 |
rs554061630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904749 | GCCCCCACAGTGCAA[C/T]TGCACGATGCTGTTT | 9873 |
rs554065078 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909914 | GGAGCACCTCTGCCC[G/T]GCTGCCCATCATCTG | 9873 |
rs554085555 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142361 | GGAGGAAGGTGGCGC[A/C]GCTCTCCCCGCTAGG | 9873 |
rs554091199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040058 | ATGTTTCCTAAATAA[G/T]AGTTTCATATTATTT | 9873 |
rs554098740 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043688 | CCAGCCTCCTTTAAA[A/G]TTAGATGTGACTATG | 9873 |
rs554101731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064175 | ATTGAACAACCTGTT[C/T]CTAAATGACTACCGG | 9873 |
rs554106361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882449 | TTGGGGAATAGAAGC[A/G]AACAGTTAGATAGAT | 9873 |
rs554110022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856079 | ACAAAGAATGGACAG[A/G]CAGGATTGGCCTTCA | 9873 |
rs554130476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111605 | TCCATTTACATTCAA[C/T]GTTGTTACTGATAAA | 9873 |
rs554153530 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028839 | TAGCACTTCCCCTTT[C/T]GTTCTCTCCGTCTCT | 9873 |
rs554156415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932356 | TTGTGTATTTTACTT[C/G]ACTGCTCTACACTGT | 9873 |
rs554161290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057027 | GGCGGAGCTTGCAGT[C/G]AGCCGAGATCACACC | 9873 |
rs554180777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079095 | TTATCAAACAGTGTA[C/T]TAAGGACTTGTCCAT | 9873 |
rs554189781 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003039 | TAACTATGAAGACTG[C/T]ACAATAAAAAGACAA | 9873 |
rs554192121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883125 | CAAAACAAAACAACA[A/G]CAAAAAAACCAAACA | 9873 |
rs554192391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875385 | CTATTATTTATTTGA[A/C]AGAGTCTCGCTCTGC | 9873 |
rs554193286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932909 | ATGAATAAACCTATA[C/T]TTGAGCCCCATGACT | 9873 |
rs554214941 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910086 | CCCCATCTGGGAGGT[A/G]AGGAGCCCCTCTGCC | 9873 |
rs554224529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981847 | TTAGCTGGGTATGGT[A/G]GCAGGCACCTGTGGT | 9873 |
rs554234107 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075602 | GGACGGATCACTTGA[A/G]GTCAGGAGTTCGAGA | 9873 |
rs554238596 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087274 | AAGATATAAAGAAAA[C/T]ATTTTTATACAGTTG | 9873 |
rs554242305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080167 | ACGGGTATGGTGGCA[C/T]GCACCTGTAGTCCCA | 9873 |
rs554246989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927887 | ACGCTCTACTTTAGA[C/T]GCAAGACAGGAATGA | 9873 |
rs554271660 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134826 | AATATACTGTTTTCT[-/G]GGGGGGGAGTTTGTT | 9873 |
rs554278555 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027382 | GAACTTTGAACTTGA[A/G]AGAGATGATTTAGGG | 9873 |
rs554293617 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108157 | ATGCATTTCTCTGAT[C/G]ATCAATGATGTTGCA | 9873 |
rs554310243 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121428 | GCCTCATAAAGCATT[A/G]TAAATATATAACTTT | 9873 |
rs554311730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081088 | TCACTTTTCATAAAA[C/T]TTAATGTAGTATTTT | 9873 |
rs554311797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071433 | GCAGTGGCTCACGCC[C/T]GTAATCCCAGCACCT | 9873 |
rs554316996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113403 | AGACAAGGTCTCACT[C/T]TGTCACCTAGATTGG | 9873 |
rs554325142 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025977 | GTTTTGACTAAAGAA[G/T]TATAGAGATTCATTT | 9873 |
rs554332729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867319 | AGAGTAGAAAAAGCC[A/C]TGGACTTGAAGTAAG | 9873 |
rs554341708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110837 | CTTCGTACTGCTGTC[A/G]TTGTATCTCATGGGT | 9873 |
rs554342381 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014642 | CAACAGCTTGATTTC[A/G]TATTCAGACTCTAAA | 9873 |
rs554362852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135262 | TACAGGGGAGAGTAC[A/T]GTAGTATGGAAATCA | 9873 |
rs554371980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907079 | CCCTTGTAAGTTGGA[C/T]TCCTAGGTATTTTAT | 9873 |
rs554372238 | snp | A/C | 0.0850919 | 0.187897 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913826 | ACCAAAAAAAACCCA[A/C]AAAAAAAACAAAAAA | 9873 |
rs554374634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910350 | AGCGACCATCGAGAA[C/T]GGGCCATGATGACGA | 9873 |
rs554379072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962703 | AGATGGTTAAACAAA[C/T]AGCTTTGTAATTTAA | 9873 |
rs554380239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112675 | TGTTGTTGAGACGGT[C/G]TCTCGCTCTGTCGCC | 9873 |
rs554382791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864889 | AGCTGCATGCAGGCT[C/T]CAGACACCTGCAACT | 9873 |
rs554385457 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072878 | CAAGTCTTCATAATT[G/T]TATTTCTTAAAAGAG | 9873 |
rs554388293 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022986 | AGAACAATTGAATGA[C/T]CATAAACAACAACAA | 9873 |
rs554388603 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056991 | GGGAAACTGAGGCAG[A/G]AGAATGGCGTGAACC | 9873 |
rs554403566 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114901 | TGAGGGAGGGGTGGC[-/A]CAAGTACTCCCTCGG | 9873 |
rs554415957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963600 | ACCAGGGACCAGTTT[C/T]GTGGAAGATAATTTT | 9873 |
rs554423637 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142013 | GAAGCAAGACTTGCC[A/C]CGGAGGGAGCAGGCC | 9873 |
rs554451821 | in-del | -/AGCCTCCCAA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053097 | TGATCTGCCCACCTC[-/AGCCTCCCAA]AGCCTCCCAAAGTGC | 9873 |
rs554459709 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921120 | GTAGCAGTTATGAAA[C/T]GCGTATTTTTAAAAA | 9873 |
rs554496698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052442 | CCTGTCTAAACAGTA[C/T]GTTTAGTGACAATTA | 9873 |
rs554503489 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144312 | CAAGGTCAAGAGATC[A/G]AGGCCATCCTGGCTA | 9873 |
rs554503723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955248 | TAGTTTGCTATAGTG[A/G]GTCACAGAACCCAAG | 9873 |
rs554520620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860666 | CGTGGGCAACATAGT[A/G]AGACCCCATCTCTAC | 9873 |
rs554526642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104730 | CGTGCCACCGCACCC[A/G]GCTAATTTTTGTATT | 9873 |
rs554558189 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052997 | GATTACAGATGCCCG[C/T]CACCACACCTAGCTA | 9873 |
rs554558413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841074 | TTGGGATACTGAGGC[A/G]GGAGGATTACTTGAG | 9873 |
rs554560901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036385 | TTCACAACGTTATAT[C/T]GGTCTTTGGAGTCAA | 9873 |
rs554565870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950858 | CCTGGGCACATGCTG[C/T]GGGACTACACTTCCT | 9873 |
rs554565894 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119614 | ACCATACCTGGCTAA[A/T]TTTTTTTATTTTTTT | 9873 |
rs554582326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899660 | AAGGACTGCTCGAGC[C/T]CAGGAGGTTGAGGCG | 9873 |
rs554595579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982615 | TCTTCTCTTTATTTC[A/G]GTGAAAGTTAAAGAC | 9873 |
rs554602939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937173 | AAAGGCTTGATGAAG[A/G]AACTCTTAAGGCTTT | 9873 |
rs554621742 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875247 | CATCTTTGGTACCTT[-/A]AAAAAAAAGCTCCAA | 9873 |
rs554627256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127301 | CCAAAAAGATCAAAT[A/G]GAATGTTAAAACAAA | 9873 |
rs554630388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974042 | ACTGGGAAAAATGAC[C/T]AGCAGAGTTGATAAC | 9873 |
rs554643529 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083859 | AAAGGACAATATTTT[A/G]TTCATCTTTATGTGC | 9873 |
rs554645169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008051 | AAGACAACTCAGGAC[A/G]ATGTGATTAAGGGCT | 9873 |
rs554654880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920165 | AGACACAACACTGAG[A/G]AGCAGAATAAAGGTC | 9873 |
rs554683129 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947110 | TGGTTTAACAGCTGC[A/T]TGCCCCATGGGGCCA | 9873 |
rs554684669 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929802 | GTATTTAAAACACTA[C/T]ATTGAAACCATTTAT | 9873 |
rs554685637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952157 | ACTTTAACTTATATT[G/T]GTCTTGCTTGGTCAC | 9873 |
rs554722760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944955 | AGGAAGAATCAATAT[C/T]GTGAAAATGGCCATA | 9873 |
rs554726294 | snp | A/G | 4.19992e-05 | 0.00458234 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867904 | CACTGCAGGAGGGCG[A/G]GCCCATCGCTCATTT | 9873 |
rs554727505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930433 | TTTTAATTTAGAGAT[G/T]CATCTCTATATTTTC | 9873 |
rs554731523 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931694 | TGCTTGGACCCGGGA[A/G]GTGGAGGTTGCAGTG | 9873 |
rs554740294 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994192 | AATGCTAGATGCTTC[C/T]CTACTGGCAAATTGT | 9873 |
rs554765755 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838369 | AATTCTCAATCAGAT[A/G]AGCAAAAGCCACTTG | 9873 |
rs554771205 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052708 | TCATCTTATATATTC[A/G]GTATTTTTAATAATC | 9873 |
rs554772383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075613 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 9873 |
rs554774469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965956 | GATACAATCTCAAAA[A/T]TATAAACATCGGCAG | 9873 |
rs554784810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076852 | GCAGTGCCTCACGCC[G/T]GTAATCCCAACACTT | 9873 |
rs554788262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892893 | ACAGGTGTGAGCCAC[C/T]GTGCGTGGCTGGTAA | 9873 |
rs554799226 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939916 | AGCCACCATGCCTGG[C/T]CTTGACGGCTCTTTG | 9873 |
rs554813415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931038 | TGTATCAAAACATCT[C/T]ATGTGCCTCACAAAT | 9873 |
rs554815346 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958290 | TGGAAGGCTGAGGCA[A/G]GCGGATCACTTGAGG | 9873 |
rs554826097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967848 | TGTAATCTCAGCACT[G/T]TGGGAGGCCGAGGCG | 9873 |
rs554827121 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878302 | CTCTAAAAATAAGTA[A/G]AATCCCTCTAATTGT | 9873 |
rs554840583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060394 | TTGTATAATTTCATT[C/T]CAAACATTCTAATAC | 9873 |
rs554855887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851969 | GCAGTGTCAACCTCC[C/T]GGGCTCAAGCAATCT | 9873 |
rs554857121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090428 | GACGGGGTTTCACCG[C/T]TTTAGCCGGGATGGT | 9873 |
rs554885498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951505 | TAGCTCAATAAATGT[C/T]TGCTCTGGTGTTATT | 9873 |
rs554902205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959105 | GAGACAAGCCACTTG[A/C]GATTCACAGGCTTAG | 9873 |
rs554903394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900396 | TTAAGGCAAACAAGG[A/T]CACAACACCTAAGAA | 9873 |
rs554918012 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082286 | AAGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC | 9873 |
rs554926830 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981286 | GACCTACCCAATGCT[A/G]ATCAAATATATGCAT | 9873 |
rs554935696 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015440 | AAGTATCAGTGAAGA[C/T]GGCAGAACATATACA | 9873 |
rs554942283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140213 | ACATCTGTCAGAATA[C/T]GTCTCTTGCTCGCCT | 9873 |
rs554945608 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977222 | CCACTACACCCAGCC[A/C]AAAACTATTAAAATA | 9873 |
rs554967903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068445 | TACAGTAAACCACCA[C/T]GGCACACAAAATTTA | 9873 |
rs554967991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923460 | CCTTGCCAACACTTA[C/T]TCTTTTGTATTTTGG | 9873 |
rs554971816 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944289 | TATAAACAGAACCAA[C/T]GACAAAAACCATATG | 9873 |
rs554985167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999062 | GTCTGAATTCTAATA[A/C]CATCATTTGAACCCC | 9873 |
rs554991313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108518 | CCTAATGTTTTCTTT[C/T]AGCAGTTTCATAGAT | 9873 |
rs555000641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940536 | GGAGCTATGGAGAAA[C/G]AAGTAGTCTCATGTC | 9873 |
rs555008867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065761 | ATTCACAATCGCTAC[A/G]AAGATAATAAAATAC | 9873 |
rs555052593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100857 | TTTTAGATGCTTCTA[C/T]GTGGGATTTTTTTTT | 9873 |
rs555060784 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125293 | AGAAAACTAACATTA[C/T]ATTACGAGGTTTATA | 9873 |
rs555085263 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142248 | CGCGCTCCCGGTCGG[A/C]CGCCTGCGCCGCCGC | 9873 |
rs555091405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134382 | GGCTGAGGTAGAAGG[A/T]TCACTTAAGTCTGAG | 9873 |
rs555093798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846149 | TGTTTTCCCAGACTA[C/T]TCATGATGAGTAAGC | 9873 |
rs555096855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848681 | TCATAGTCTATTTAA[C/T]GCAGGGATGTGCCTG | 9873 |
rs555104995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895947 | AAAGAGCCACCCATA[A/G]CAAAGAGAATTTTCA | 9873 |
rs555105982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992024 | ACCCCATCGTCTCAG[C/T]CCAAAATCTCCTTAA | 9873 |
rs555109778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044006 | AAATAAATTTCTTTT[C/T]ATAAGCCTCAGTGAT | 9873 |
rs555118712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088968 | AAGGAATAGCTTTTG[A/T]ACCCTTGATGTGCAT | 9873 |
rs555121342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104662 | CAACCTTCACCTCCC[A/G]GGTTCAAGCCATTCT | 9873 |
rs555121955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085697 | AGACTACCTACAACA[C/T]TTAAAAACTTTTTAA | 9873 |
rs555124371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884269 | CAATCTAACAAACAC[A/G]TAAAGCCAGTATTGC | 9873 |
rs555141767 | in-del | -/A | 0.319855 | 0.240042 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049875 | ACAAAAGGACCATAA[-/A]AAAAAAATTGTTTTC | 9873 |
rs555154787 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73141929 | GTTAGCAAGGACCAG[A/G]AGGAGGAGGAGGGCC | 9873 |
rs555184511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096781 | TTCCCCAGCCTAGAC[C/T]GTGTCACTACACTCT | 9873 |
rs555185906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090095 | TGAATTATCAGTAAA[C/T]TGTGTTGGGATAACT | 9873 |
rs555186143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081260 | CCACTATGGTGAAAC[C/T]CCAACTCTACTAAAA | 9873 |
rs555207661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869817 | TCTAACCCATTTCCT[A/G]GACTTTTTCTCCTCT | 9873 |
rs555211645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922444 | GAAAAGTGACTCAGA[C/G]ATACTGCTTTGGGGA | 9873 |
rs555219984 | in-del | -/A | 0.0952156 | 0.196321 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967200 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 9873 |
rs555223600 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112857 | TTTTAGTAGAGATGG[A/G]GTTTCACCATGTTAG | 9873 |
rs555224908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971173 | TAAGTAACTGGAACA[A/G]GTCAAAATATAAAAA | 9873 |
rs555246879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985476 | ACTTCATACACTTTA[A/G]TTCCTGCAAAGGTTA | 9873 |
rs555251238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877888 | GCACATGTCTGTAGC[C/G]CCAGCTATTCGGGAA | 9873 |
rs555269153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858327 | GCACATGCATGTTCA[C/T]TGCAGCACTATTCAC | 9873 |
rs555275588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023960 | GGAAAGACCAATTGA[C/T]AGAGAAAACAGATCA | 9873 |
rs555282918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034409 | GCAAAAACGTTCCTC[G/T]TCCTGAAAGAAGCAA | 9873 |
rs555287938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878542 | TAAGGTGAACACTGT[C/G]ATAGCTTGTTTTACT | 9873 |
rs555311297 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963869 | CCATGGACTGCTGAG[A/G]TCCAAGGCCCTGGGG | 9873 |
rs555315584 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971781 | TAAGCAGAGAACCTG[G/T]CTAAGCCTACTTGGA | 9873 |
rs555326549 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017858 | AAAATGTGAAAAGCG[C/T]CATTGCCTAGGTACT | 9873 |
rs555341544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926143 | AGTCCTGGGCAGAAG[A/T]GGGTGGGTTCCCAGT | 9873 |
rs555381610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002472 | AACTTGCAATGTAAA[C/T]TCACCACAGGCTCTC | 9873 |
rs555383091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857126 | GTTGATTTTTGGATT[C/T]CCATGGAAGGCAGTA | 9873 |
rs555391633 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096461 | AAGGCTGAGGCAGGA[A/G]AATCACCTGAACACA | 9873 |
rs555392168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111496 | CTATGTGTGTCTTTA[C/T]AGGTGAAGTGTGTTT | 9873 |
rs555396927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857778 | TTATTGCAGAGGCAG[A/G]AAAGATGATCTTTTT | 9873 |
rs555405013 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999135 | AAGCAGATACATTCC[C/T]TTCTTGGCTTAAAGC | 9873 |
rs555439571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072879 | AAGTCTTCATAATTT[C/T]ATTTCTTAAAAGAGT | 9873 |
rs555444484 | snp | C/T | 0.000400105 | 0.0141383 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841471 | TTTGCTGAAGGAGAC[C/T]GGGGAAAGTACAGGG | 9873 |
rs555453840 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865229 | TTCTGCTTCATGTTC[C/G]TCAGCCAGCTAGCTG | 9873 |
rs555456978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858477 | TTGGAGGGACATGGA[C/T]AGAGCTGGAGGCCAT | 9873 |
rs555460382 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987509 | ACCATATCCAATATA[A/G]AGTATTCAACAAACT | 9873 |
rs555466998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105446 | TGGTAACATTACTTT[C/T]CTAGGGAAGAACTCC | 9873 |
rs555505004 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065232 | AAATGTAATCTATCA[A/C]GTAAACAGAATCAAT | 9873 |
rs555505279 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019389 | GTAACTAGTTAGGTG[C/T]GAGCTAGAATCCAAA | 9873 |
rs555512999 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098035 | CCAACTTTAGTTTCA[C/T]TGATTCTCTTCATCA | 9873 |
rs555520894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997074 | AGCAAGTCCAAAAAT[A/C]TGTATGCAATTTCCC | 9873 |
rs555533636 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889249 | TACAGGCGTGAGCCA[C/T]CGCGCCCGGCTATAA | 9873 |
rs555551111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138558 | ATAAGTTAAAAAAAC[C/T]TTACATTTTTAACCA | 9873 |
rs555552351 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960787 | ATAAAGAACCCCAGG[G/T]TGTGAAATACACTCT | 9873 |
rs555561038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880238 | CAATTGCTATCAAAA[C/T]CAATGACATTCTTCA | 9873 |
rs555561397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888649 | TTGGAGACAGGGTCT[C/T]TCTCTGTCACCCAGT | 9873 |
rs555568428 | snp | G/T | 0.021333 | 0.101051 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056439 | TAAAAATTATTTTTT[G/T]TCTCCCTAGATTCTA | 9873 |
rs555571840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851137 | AAAGGTTGCTAAGTG[A/C]TACCAAGGATGTGGA | 9873 |
rs555573324 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076786 | TGTAATGTATTGATA[C/G]TACTAGAAGCTGGGT | 9873 |
rs555590276 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036778 | TCAAGAAGTCTTCCT[C/T]CACAAATATTGTGTT | 9873 |
rs555597220 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004041 | CTTGAACTGGAAGGC[A/G]GAGGTTGCAGTGAGC | 9873 |
rs555601421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035110 | CAGGTTTAACTCCTG[A/G]ACCTTGACAAGTTAT | 9873 |
rs555613182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949221 | TGGGAGGCCCATGGC[A/G]GGCAGATCACCTGAG | 9873 |
rs555629366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136959 | CTTGTACCCAGGAGG[C/T]GGAGGTTGCAGTAAG | 9873 |
rs555651592 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068827 | GTAAAAAAAAAAAAA[A/G]AAAAAGAAAAAGAAA | 9873 |
rs555660055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989942 | AGGACTATTGTGCAA[C/G]GGTGAATAGTGTGGA | 9873 |
rs555668392 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000846 | CTTAATGAGAACATG[-/T]TGAAATCAGAAAATC | 9873 |
rs555671569 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902467 | CTTTTTCTGTCTGTC[A/T]ATGCCAAGGGTAACT | 9873 |
rs555673502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027605 | GAAGAGAAATTCAAG[C/T]TGGCTGCAGAAATTT | 9873 |
rs555678942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897665 | ATAAACTGCTAGTTT[A/G]GACACCCAAACCCAT | 9873 |
rs555683353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881690 | ACACAATGGAATACT[A/G]TTCAGTCATAAAAAA | 9873 |
rs555704222 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874271 | AGCTCACTGCAGCCT[A/C]GAACTGCTGGGCTCA | 9873 |
rs555710924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129569 | TCTCCCACCAACCCC[A/G]GATGGGACCGTCCAG | 9873 |
rs555711610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966936 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 9873 |
rs555713603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976246 | AGTATTTCTTGGGGA[A/C]TCTGTCCAAATACTT | 9873 |
rs555714737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917849 | GCTGAGCTCATGCCA[C/T]TGCACTCTAGCCTGG | 9873 |
rs555714802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843003 | ACTTTAGGGTTCTAC[C/T]GTGCAGGACAAACGT | 9873 |
rs555724944 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892113 | GGCAACTGATAGAGA[C/T]ATTTAATTTTTGTTA | 9873 |
rs555732594 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935285 | TGTAATTTCCCCTAA[A/G]GTAAGAACTTTAAAC | 9873 |
rs555733574 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098605 | AATTGATAGTCCAGG[A/G]AAAAAAAAACAAACA | 9873 |
rs555750349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967776 | TGGTATGTGAATTAT[A/G]TCTAATTTTTTTTAA | 9873 |
rs555769646 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115310 | TGGAAGAGGGGTGGC[A/G]TTGGCAATTCAAGAC | 9873 |
rs555770234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042813 | TTTTACTTTTTTCTA[A/G]CTATTATAAATTTGA | 9873 |
rs555771851 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136801 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACTTGAG | 9873 |
rs555783161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860755 | CCTGGGAGGAGGAGG[C/T]TGCCGTCAGCTGAGA | 9873 |
rs555789587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020258 | ACACTAGGAAATGGA[C/T]TGATGGCTTAACCTT | 9873 |
rs555791293 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031029 | ATACTATTCAGCCTT[-/A]AAAAAAAAGGGAGAT | 9873 |
rs555795310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861658 | GGATAGGCCGGGCGC[G/T]CTGGCTCATGCCTGT | 9873 |
rs555799181 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976208 | AGTATCTGCTCTAGT[A/G]ACTACTGGCATAAGA | 9873 |
rs555802084 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975963 | ACAAAGAAAATATTT[-/C]ACAAGCTTCTAAAAA | 9873 |
rs555813976 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911863 | TTTCATTTTAAGAGA[A/C]CTTTCACTTCTTTGG | 9873 |
rs555818730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065889 | ATATTCCATGCTTAC[A/G]GCTAGGAAGAATCAA | 9873 |
rs555833081 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035921 | AGACAGGGTTTCACC[A/T]TGTTGGCCAAGATGG | 9873 |
rs555845895 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013376 | GTTTTCTTCTATGGC[C/T]CCAGTGCCCCTCTCC | 9873 |
rs555853456 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916361 | GTCACCCAGGCTACA[C/G]TACAGTAGTAGCATG | 9873 |
rs555855479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877764 | ATAATCTCAACACTT[A/T]GGAGGCTGAGGCATG | 9873 |
rs555855927 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972896 | AACAATGCTGAAAGG[C/T]ACAATAAAAGGATTG | 9873 |
rs555856751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853736 | ATAAATTGAACCTTA[A/T]CAAAATAAAAAATAT | 9873 |
rs555858376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008293 | GCAGTGGGCCAAGAC[C/T]GTACCACTGCACTCC | 9873 |
rs555860059 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088613 | AAAAAAGTCCTTTTT[A/T]AAAAAAATGCACATT | 9873 |
rs555862220 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956929 | CACTTCTTCATGTGA[A/T]ACATAGAGAAGACAC | 9873 |
rs555868653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108703 | CCTCCCGAGTAGCTG[A/G]GACTACAGGCGCCCG | 9873 |
rs555884322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938677 | GAGGGTCAATTTTCA[C/T]CATTCTTTTACTCGT | 9873 |
rs555898022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114515 | AGTTTCTCACTGTAG[C/T]CACCATAGCTGGAAA | 9873 |
rs555909277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005007 | TCCTATTACTTGCAC[A/G]AACTACCTGTGCTCT | 9873 |
rs555917295 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032044 | TACACAATTATTAAA[A/G]AGAATGTGCTATATA | 9873 |
rs555929156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869647 | GTGATGCTGAAGTGA[A/G]CACATACTTGCATTT | 9873 |
rs555930397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109212 | GCTATTCTGGGTCTT[C/T]TGTGGTTCCATATAT | 9873 |
rs555946234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949632 | ATCATACAATATATA[C/T]GCTTTTGTGTCTGGC | 9873 |
rs555957261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049294 | AAAATTAAAACATGA[C/G]AGAAACTGTCTCATA | 9873 |
rs555973174 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854526 | AGCTTTGAACTCCTG[A/G]ATGCAAGGGATCCTC | 9873 |
rs555977069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893205 | GGGGGTTTTGCTATG[A/T]TGGCCAGGCTGGTCT | 9873 |
rs555982518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069455 | TATATACATACATAC[A/G]TATATACACACATCT | 9873 |
rs556010446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050665 | TCCATATCCACATGG[A/G]GAGATAATGGGAACA | 9873 |
rs556017617 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843653 | GAAACATGTTGAACA[C/T]AAAAATTTAAATGCT | 9873 |
rs556018354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942062 | TCAAAATCTCATGTC[A/G]AAATGTGATCTCCAA | 9873 |
rs556022297 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113649 | GTATTTATTGTAGTC[A/G]TCATAGTCTGGGCTT | 9873 |
rs556031439 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893150 | ATTACAGGGCATGTA[A/C]CACCATGCCCAGTTA | 9873 |
rs556039979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099072 | AAAAAATTAATTAGT[C/T]GGAGGTAGTGGTACA | 9873 |
rs556042463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993653 | CTCAGCAGACTATCG[A/C]AAGGACAAAAAACCA | 9873 |
rs556049930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960725 | TCTGCTTTGATAATG[C/T]TGGGAGTTGATGTGG | 9873 |
rs556053624 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084443 | TTGCCTAGGCTTGAG[A/T]GCGGCGGTGAGGTCC | 9873 |
rs556054959 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858801 | ATGCTAAAAATATCA[C/G]GAAAATGGATTTGTG | 9873 |
rs556055311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942945 | TCCCAAAGTGCTGGG[A/G]TTATAGGTGTGAGCC | 9873 |
rs556061897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009091 | AAAAGTCTAATGCAA[A/T]TTGAGGTTTTAATGA | 9873 |
rs556070649 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007861 | TACAGTTATGCAAGA[C/T]ATTACCACTGGGAGA | 9873 |
rs556088546 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953073 | GTTATTGTGCTCCAA[C/T]AGAAAATAAAATAAA | 9873 |
rs556105691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869135 | TGGTGTCGAACTCCT[A/G]ACCTCAGGTGATCCA | 9873 |
rs556115407 | in-del | -/AATG | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884246 | TTATACAACACAGTT[-/AATG]AATGGGTCAATCTAA | 9873 |
rs556121411 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902154 | TGCTGAGATTACAAG[C/T]GTGAGCCACAGCGCA | 9873 |
rs556132527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937878 | CAGTTATTATGCTAG[A/G]CACCATGGGAAATAC | 9873 |
rs556139353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943501 | AACAGTAAATGTGAA[C/T]TTCATATTACCTTGG | 9873 |
rs556140271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032146 | ACATGTAAGCATATA[C/T]ACTCTAGAATACATA | 9873 |
rs556141257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935597 | GAAGACCCCAAGCTA[C/T]GCCTAATCAGGTTAC | 9873 |
rs556179572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016110 | GAGTTTGAGACCAGC[C/T]TGGCCAACATGGTGA | 9873 |
rs556180687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846820 | ATAATTGAGCTCTTA[C/T]GGTACATACAATTTG | 9873 |
rs556183038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886582 | TTTAATGGCTGGATG[A/G]TGTCAGTCTTTTATA | 9873 |
rs556183669 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935502 | AGTTGTCTTAAAATT[A/C]AATCATGAAATTCTA | 9873 |
rs556183871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023911 | CAAATTAAAAAGGTT[A/G]CACACTGTATTATTC | 9873 |
rs556194744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839243 | CAAAAGAGAAGGCTA[G/T]AAAGGTAGGCTAGGG | 9873 |
rs556200743 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102635 | AGATGATTAGGCCAT[C/G]AGGGCTCTGCCCTCA | 9873 |
rs556211938 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859397 | ACCATATCACGGTGC[C/T]TGTGTTCAAGTAGCC | 9873 |
rs556219303 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905282 | AAAAAGTTTTAACTT[C/T]TAATCTCTGTGGGTA | 9873 |
rs556223311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046144 | TAAAGACACACACCA[C/T]GATGCCATGCTGATT | 9873 |
rs556245422 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972050 | TTAATTGTACCTCAA[C/T]AAAATTGATTTAAAA | 9873 |
rs556273261 | in-del | -/TTTG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892606 | TGTGTTTTTGTTTGT[-/TTTG]TTTTTTGTTTTTTGA | 9873 |
rs556279890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137847 | GCATGAAACGGTAGT[A/G]ACTAAGCCAGGAAAG | 9873 |
rs556281855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061289 | AGATACTGTGCTTGT[C/T]GCATGGTTTTCGCAA | 9873 |
rs556282348 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888156 | CTGAGAAACTGAATA[G/T]TTCATTGTGGGATGG | 9873 |
rs556284610 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039927 | TAATATTCATGAGGA[C/T]ATCACAAAAGCAGTT | 9873 |
rs556290235 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046816 | TTGAACTCCTGGCCA[A/G]AAACGATCCTCCTAC | 9873 |
rs556322105 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009764 | CTGCTGAGAAATCTG[C/T]TAGTAGTCTCATAGC | 9873 |
rs556323221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901275 | AGTGGTGCGTGCCTG[C/T]GGCCCCAGCTAATCG | 9873 |
rs556335296 | snp | C/G | | | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836342 | GGCATCCAGAATGCC[C/G]GCTTCCTGGAAGCCA | 9873 |
rs556337846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932210 | CCAACCCCTCCTCCT[A/G]ATCTCCACAGCTACT | 9873 |
rs556344952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053398 | TGAAAGATAGAAAAT[A/G]AATTCTGAAAAAAAT | 9873 |
rs556355312 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061712 | GGAAGTTCGAACTGG[A/G]TGGAGCCCACTGCAG | 9873 |
rs556364589 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100441 | CAATCTCGGTTCACC[A/G]CAACCTCCACCTCCT | 9873 |
rs556366629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978174 | CATGGGGTGGGGGGA[A/G]CGGGGAGGGATAGCG | 9873 |
rs556378271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101987 | CAGGGTAGGCCAGAA[A/G]CTGCAGACCCAGATA | 9873 |
rs556381705 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006763 | TGTTTGTCTTCCCTC[A/G]TTAGAATGTAGGCTC | 9873 |
rs556398636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045532 | CCAGATGTCCAACAA[C/T]GATAGAATGGATTAA | 9873 |
rs556412342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916359 | CTGTCACCCAGGCTA[C/T]AGTACAGTAGTAGCA | 9873 |
rs556413217 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838539 | ATGAGGGCTGCCCCC[C/T]TCTTTGCTCCTAGGG | 9873 |
rs556414063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945204 | ACCAAAACAGAGATA[C/T]AGACCAATGGAACAG | 9873 |
rs556427544 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143359 | GAGGCAGGAGAGGCC[A/G]TAGAGGAAGCCCTTG | 9873 |
rs556439493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094447 | GAAAACGTGTCCACA[A/G]AAACACTTTTACAAA | 9873 |
rs556444314 | snp | C/G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039724 | CATTATCAAGGATAA[C/G/T]GAATGATGCAGGACT | 9873 |
rs556446174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909881 | CTCTGCCCGGCAGCC[A/G]CCCCATCTGGGAAGT | 9873 |
rs556453953 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000221 | ACACTGGATGGCTTC[C/T]AAAATATTATTTCCC | 9873 |
rs556471418 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870252 | AAGCACTCTATATAG[A/T]TCTAATTACAATGTG | 9873 |
rs556480640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985719 | ATGATGTAATCTTCT[A/C]CCACTCTTGGGTTCT | 9873 |
rs556490456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071594 | TAGTCCCAACTACTC[A/G]GGGGGCTGAGGCAGG | 9873 |
rs556497422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889294 | AAATATGTCTTGAGG[A/G]ATGAAAACTTATATT | 9873 |
rs556500228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136015 | AATCTTTAAAATAAG[C/T]CAGGCATGGTGGCAC | 9873 |
rs556528301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938894 | GTTTTTGAGTTGCAC[C/T]CTAAAGCTGATTTAA | 9873 |
rs556539640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931412 | ATGCCCAGCCTTAAA[A/T]TTTTTTTTTAAATAA | 9873 |
rs556540316 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035189 | GTATGTATGTATGTA[C/T]GTATGTATGTATGTA | 9873 |
rs556579377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086342 | TGAACCCAGAGGTGG[A/G]GGTAGCAGTGAACCA | 9873 |
rs556580983 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889690 | TGCCCTTCAACCTGG[G/T]TGACAGAGCAAGCCT | 9873 |
rs556598276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010626 | GCTTGCAGTGGTACG[G/T]TATCTGTACGATTTC | 9873 |
rs556611020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954610 | GAGTAATTCCAAGAA[C/T]ATAGTTGTCATTACT | 9873 |
rs556614838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129493 | TATTGTGAACTGCAC[A/G]TGCAAGGGATCTAGG | 9873 |
rs556615317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939570 | AAATTCTCTGGCTTA[C/T]AGGAAATCTATGAAG | 9873 |
rs556628402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120747 | AAAATAATAATAATA[A/G]AACAAAAATTAAAAA | 9873 |
rs556638237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087412 | TTTATTACTGAAGAA[A/G]GAAAAGTTTTTGGGC | 9873 |
rs556642562 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977404 | GCAGAGACAGCCCAT[G/T]GAATGGTAAAAAATA | 9873 |
rs556668263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028747 | CCTGGTGGGAGGAGA[G/T]TGGATCATGAGGGCA | 9873 |
rs556680839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070580 | AGGCGCCTGCCACCA[A/T]GTCTGGCTAATTTTT | 9873 |
rs556709403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017400 | CGTAACTAAAAAGAA[C/T]ACAATGCTGAAATGA | 9873 |
rs556726727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881866 | AGAGGCTGGGGCCGG[A/G]TGCGGTGGCTCACGC | 9873 |
rs556731400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029246 | TACGGAAACCACTTA[C/T]AAGACTATTGTAGGA | 9873 |
rs556741002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927304 | TCTGTATGATACTAC[A/C]ATGGTGGATACATAT | 9873 |
rs556759118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080105 | GGAGTTCGAGACCAG[C/T]CTGGGCAACATAGTA | 9873 |
rs556770556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010184 | TTGATCTAGTCTATT[A/G]TTGAAGCTTTCAAAT | 9873 |
rs556772498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066218 | AACCAACTGATCTTT[A/G]ACAAACCTGACACAA | 9873 |
rs556789445 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138549 | TTTGCTTAATAAGTT[-/A]AAAAAAACCTTACAT | 9873 |
rs556805983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970273 | TTAACCAACAATAAA[C/T]ATTACAGAATCTAAG | 9873 |
rs556809238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919998 | CAGTTCAAGCAGAAA[C/G]ACACTTTTTTAAAAG | 9873 |
rs556815627 | in-del | -/CTGATTATAAAATACATG | 0.0573587 | 0.15934 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947753 | TGAAAACATAATTTT[-/CTGATTATAAAATACATG]CTCATAAAGAAAATT | 9873 |
rs556823954 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903168 | TACAGCATACCAAGA[A/C]GACAGGCTAGAAAGG | 9873 |
rs556834130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848038 | CTCACCAGATTATTC[A/G]AGGCCTCCTTTTTGG | 9873 |
rs556835437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066804 | TCTCACGCCAGTTAG[A/C]ATGGCGATCATTAAA | 9873 |
rs556848974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855420 | GGCGGAGGTTGCAGT[A/G]AGCCAAGATCATGCC | 9873 |
rs556851235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074055 | CAAGATTTATTGTTA[C/T]AAAGACAAAGTACTT | 9873 |
rs556898982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059620 | GAAAAGCAAAATTAG[G/T]CTATGAAAATTCAAG | 9873 |
rs556903565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997521 | AGAAAAACCGCAGGC[A/G]GTTAAAAGAGACCTA | 9873 |
rs556906927 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127161 | CTCCAACTTGTTTCT[A/G]TGGAACCACAGACAT | 9873 |
rs556916901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965382 | ATGCACTAAAACACA[A/G]TAGGAAACAATACAC | 9873 |
rs556919977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042770 | GTTGTAGGTCTTTCA[C/T]CTCCTTGGTTAAATT | 9873 |
rs556924298 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110811 | AGGTACTTATAGCTA[C/T]GAACTTCCCACTTCG | 9873 |
rs556953889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957329 | GAGAATGATGGTTTC[C/T]AGTTTCATCCATGTC | 9873 |
rs556969208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935436 | CGGGCATTTCTAAAA[C/T]AGACTTTGGTAAAAG | 9873 |
rs556975204 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090351 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 9873 |
rs556977277 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035846 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGAGACTAC | 9873 |
rs556979079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098574 | AGTTTGTTTACAGTA[C/T]GGTTAGTTGGAATAG | 9873 |
rs556988228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906184 | CTCTGATGACCAGTG[A/G]TGATGAGCATTTTTT | 9873 |
rs556994723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851381 | CAATCTATATGTCCA[C/T]CAACAGGGGAATGTT | 9873 |
rs556998221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882244 | TCAGGAGTTCGAGAC[C/T]AGCTTGGCCAACATG | 9873 |
rs556998443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963690 | GGCATTAGATTCTCA[C/T]AGGGAGTGTGCAACT | 9873 |
rs557027961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951453 | TCAACCTTGGCACTG[A/G]CTTATACGTAAAGCA | 9873 |
rs557027988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943601 | GCACAGAAATGGAAG[C/T]GAGAATTCCCTGGGT | 9873 |
rs557040792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091210 | GTATTATGGATAATG[A/C]TGCTATCCACATTCA | 9873 |
rs557046230 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836823 | TGTAAAGAAAGCACA[A/T]CTGCACAGAGGCTCC | 9873 |
rs557064001 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853635 | GCCCAGGCTGGTCTC[A/G]AACTCCTGAGCTCAG | 9873 |
rs557086635 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875361 | AACTCTATCTATCTA[G/T]CTAGCTAGCTATTAT | 9873 |
rs557091776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117625 | GTGGTTTTGTTTGTT[C/T]TTAGTTTGCAAGCAC | 9873 |
rs557100380 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051672 | GAGATGTACTGGCTA[C/T]GCAACAATAAAACCC | 9873 |
rs557103636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116806 | CCTCTCAAAGTGCAC[A/G]GATTACAGGCATGAG | 9873 |
rs557107292 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837754 | GGTTCTTCCTTCCAC[A/G]GAAATGTCAGGGTAG | 9873 |
rs557108951 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090952 | CCTCCCCTGTCAACT[-/A]CTAATCTAATTTTTT | 9873 |
rs557111516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092805 | ATCAAGGAGGGCATC[A/G]GAGTATACAGTAAAG | 9873 |
rs557141819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132763 | CAGAAGGTGGAGATT[G/T]CAGTGAGCCATGACC | 9873 |
rs557144908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972834 | ATCACCAAGTGCCTA[A/T]CACCTAGTACAAACT | 9873 |
rs557151442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043835 | TAGAGGATCCATTGA[A/G]GACTTGAGGCCCTAA | 9873 |
rs557155966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074899 | CCTAGGCGACAGAGT[A/G]AGACCCTGTCCCAAG | 9873 |
rs557166942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115951 | TGGGTACTACAGCAT[A/G]AGCAAGTTGATACAT | 9873 |
rs557176293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022266 | AAGCCCTACTTAGTA[C/T]AATAAGGCAAGAAAA | 9873 |
rs557182064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845212 | GATCACTTGAGGCCA[A/G]CAGTTTGAGACCGGC | 9873 |
rs557194577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900291 | AGAGCACTGACAGGG[G/T]AGAGCTCAATATCCA | 9873 |
rs557198292 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990776 | GATCTAAAATTGACA[A/C]CCTAACATGACAAGG | 9873 |
rs557205080 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852461 | CCAGCACTTTGGAAG[A/G]CTAAAGTGGGTGGTG | 9873 |
rs557232816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973906 | CAGAAGCCTATTTAT[C/T]ATCTGTCCCTTTACA | 9873 |
rs557235777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014663 | AGACTCTAAACCATG[C/T]GCTTCAATACTAAGT | 9873 |
rs557236139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085584 | CAACCACATTTAAGG[A/G]AGAAATTGAAAAGTC | 9873 |
rs557236950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867253 | ATCAACCGAATTTTT[C/T]TGGTACTTAGATCTC | 9873 |
rs557243350 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060678 | TAAAAAATAAAAAGG[-/A]AAAAAACTATAAGAC | 9873 |
rs557245207 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143957 | TAATCAAATCAGGGA[A/G]GGCCTGGGGCAAGGG | 9873 |
rs557260895 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977749 | AAACTAGTTCAACCA[C/T]TGGGGCGATTCCTCA | 9873 |
rs557262661 | in-del | -/A | 0.0209421 | 0.100162 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049684 | AACTTAGAGTATAAT[-/A]AAAAAAAAAAAAAAA | 9873 |
rs557290748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958172 | GGGAAAGATGGCTTG[A/C]TTTAAATCAAGTCAG | 9873 |
rs557323089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906934 | TTCCATATGAACTTT[A/G]AAGTAGTTTTTTCCA | 9873 |
rs557335921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038154 | TTCAAGCCAAGCCTA[A/G]GCAACAAGGAGATCT | 9873 |
rs557338750 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910260 | GCCTCTGCCCGGCCA[C/T]CCCATCTGGGAAGTG | 9873 |
rs557372589 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075899 | CAACGCAGTCGGATC[A/G]CTTGAGTCCAGGAGT | 9873 |
rs557380608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107567 | GTTTATACCCATTAA[C/T]CATCCTCACTTCCCA | 9873 |
rs557391974 | in-del | -/TATT | 0.0341408 | 0.126114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914009 | CATACTGCCTTAAGC[-/TATT]TATTTATTTATTTAT | 9873 |
rs557394856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023301 | TCATGTATCTGATAA[A/G]GGAAGTCCAAATATA | 9873 |
rs557410814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930333 | TCAAAACTTTACTAG[C/T]GCCAACCTTCTCTTT | 9873 |
rs557412841 | in-del | -/AGACT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846143 | CGCATATGTTTTCCC[-/AGACT]ACTCATGATGAGTAA | 9873 |
rs557420634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954441 | AAACTCCTGGGCTCA[A/G]GCGATCCTTCCCCTT | 9873 |
rs557423798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844503 | CTGACAGCAGCAATC[C/T]ACCAGCATCAGCCAC | 9873 |
rs557432250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006731 | TGGCATATATGTTTA[A/T]TTATTCACTTGTTTA | 9873 |
rs557446435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099817 | GAGTGCGAAGGGAAG[C/T]CAGGAGAGGCGGCAC | 9873 |
rs557455660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947047 | GGCCCCAGGTGAGAT[C/T]CAGGTCCAAGAAAAT | 9873 |
rs557458068 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909452 | AGCCTCTGCCCAGCC[A/G]CCACCCCATCTAGGA | 9873 |
rs557468751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044395 | CCAGCCTGGGCAACA[C/G]AGTGAGGCCCTCTAT | 9873 |
rs557470631 | snp | C/G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865871 | TGCTACACAGTAGTC[C/G/T]AGTCATACACTGCCA | 9873 |
rs557493393 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991353 | GGGAATCCTCCCTAA[C/T]TCATTTTATGAGGCC | 9873 |
rs557504794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855400 | AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 9873 |
rs557521446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140472 | TATTTCTAAAAAAGA[G/T]TCAAAGACATTAACC | 9873 |
rs557525477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110687 | TGCTCCGATCTTTAT[A/T]ATTTCTTTTATTCTA | 9873 |
rs557546958 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937085 | AAGAGGAGTTCTTCC[C/T]TAGCTGTGGTCCTGA | 9873 |
rs557548505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891704 | TCAGATAGACTTAGT[C/T]TGAATCCATTGTATG | 9873 |
rs557559673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132391 | TTCACACATACAAAA[C/T]ACTGAAGCTCAGAAA | 9873 |
rs557575429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096698 | GTGTTCAGTCTTTCA[A/C]CACTGAGTACGATGT | 9873 |
rs557580827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983550 | AATAAAAAATTCAGG[A/C]TAAGAGATACACTAT | 9873 |
rs557586495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104003 | ATACTAATACAAAAA[C/T]ACAAATAAATGTTTT | 9873 |
rs557590907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929660 | TCTCAACATGGTTTG[C/T]GATTAGAAGGCAGAT | 9873 |
rs557591358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037439 | TCTGCTATTTGTCCC[G/T]TCCCCTTCATCCTCA | 9873 |
rs557595664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854510 | GATCATAGCTCATTG[C/T]AGCTTTGAACTCCTG | 9873 |
rs557597426 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888127 | AAGAAAACAAGATAG[C/G]CAAGTATAGGAATCT | 9873 |
rs557608941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047301 | ATATCTGGTAGAAGC[C/T]ACATACCTAAATGAT | 9873 |
rs557613540 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957023 | AGGACTCTAGTCTTT[-/T]TTTTTTTTTCTTCTT | 9873 |
rs557615504 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877004 | TAGACAGGGTCTGGA[C/G]TTTGTTGTCTACGCT | 9873 |
rs557621100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140182 | ATTTAACCCAAAAAA[A/C]TTGCTTCAGGAAAAT | 9873 |
rs557628106 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889546 | AGACCCTATCTCTAC[-/A]AAAAAATCTAAAAAA | 9873 |
rs557631885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123315 | TCCTAGCCAAGCCAG[C/T]ATTTCCTGGAATCCC | 9873 |
rs557650650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030399 | TTTCACAACTGAATA[C/T]ACAAAACTCAATTTA | 9873 |
rs557658681 | in-del | -/CT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885106 | TAATTCCTTTGAAGA[-/CT]CTCATGGTCTAGTCC | 9873 |
rs557668574 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113239 | TCGAATTTCTTAGAG[A/T]TTCCTCAAAATAGCT | 9873 |
rs557683640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970367 | GAAAATTGTCTTTTA[A/T]CTAAAAGCCCTACAA | 9873 |
rs557683699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980084 | GAGACTCTGGAAGAG[A/T]CTTCAACACAGATGA | 9873 |
rs557684185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940491 | AGTAGCCATCAGGTA[A/G]GCCAAGATGGGTGCA | 9873 |
rs557698165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872500 | TACTTTCTGTCTATA[A/C]AGATTTGCCTATTCC | 9873 |
rs557700115 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054147 | TGCTTACACTCTACA[A/G]CAGCAATGTTGGGAA | 9873 |
rs557715470 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093664 | TGGAGTGCAATGACG[C/G]GGTCTTGGCTCACCA | 9873 |
rs557719330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932985 | GTTAAAGGAGTAATT[A/G]ATTTCATAAAACTCT | 9873 |
rs557737022 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085966 | GCAGATCTACTAAAC[A/T]AAGATACTAAAACAA | 9873 |
rs557748468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880059 | CCCAAACCAAACCAA[A/G]ACAAGACAAAAACAA | 9873 |
rs557754938 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117500 | ATTCATTAAGAGCTA[C/T]AAATTTCCTTTTGAA | 9873 |
rs557767089 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004457 | CCTTTAGAATTCTGA[A/C]TCTAACAGTTACTCA | 9873 |
rs557767380 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966230 | AGTGGTGCGATGTCG[A/G]CTCACTGCAACCTCT | 9873 |
rs557767739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971102 | TGAAGGCAAACTAAA[C/T]GCTGTTGTTTTAAGC | 9873 |
rs557775663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864204 | TTGTGGGCTATAGTT[C/T]GAAAATGTAAGCAAT | 9873 |
rs557785507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009998 | AATAGATTTTTCTAA[C/T]CTTCCCTTCCCTCTT | 9873 |
rs557788262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865052 | TCCTTCCTTATTCTA[C/T]AAGGGAGTAGTCTGT | 9873 |
rs557843444 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957714 | GTAATCTTGCATGGC[A/G]GATATAAATTCTGGA | 9873 |
rs557845417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011524 | TTAGCCCTAGTGATG[C/G]TGGACCCCAGGACAG | 9873 |
rs557846856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010567 | TTTCCTGAAGATAGA[A/T]CTATGGTGTTGTTTG | 9873 |
rs557849726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903736 | CCATTAGCACCTCTG[A/C]TAGAAGATGGGCAGA | 9873 |
rs557858278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994377 | CTTGAAACGACTCTA[C/T]GAAAAAGGTAGTAGT | 9873 |
rs557858658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027565 | GCAGCCTGACCATGA[C/G]GTAGAAAAGAAAAAC | 9873 |
rs557860424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939872 | GATCTGCCCACCTTG[A/G]CCTCCCAAGTGTTGG | 9873 |
rs557888795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886869 | TCTAAACACTACACA[A/G]AATGTACATTTTTGT | 9873 |
rs557896566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123141 | ATAAACAAGCCAAAC[C/T]GCCACTCTCTTTATC | 9873 |
rs557906747 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003116 | GCAGATTTATAGCAG[C/G]GAAACATATCCTGAA | 9873 |
rs557908623 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012651 | TCTTTTTCACAATAG[C/G]ACCACCATCCTCTCA | 9873 |
rs557917166 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917338 | AAACCTTTTTCTGAA[A/G]AGAATATTCTTTCTC | 9873 |
rs557942678 | snp | G/T | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141515 | AGGCTCTGCAAAGCT[G/T]CAGGGGCGTCCCCGC | 9873 |
rs557947380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963697 | GATTCTCATAGGGAG[G/T]GTGCAACTTAGATTC | 9873 |
rs557955088 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954706 | AGGCTGGTCAGGAGA[C/T]GAGTAGTGTACAAAG | 9873 |
rs557962501 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896896 | CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCCC | 9873 |
rs557962577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857674 | AGGCTGGTCTTGAAC[A/T]CGTGACCTCAGATGA | 9873 |
rs557976694 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099334 | TGAAGAAATTAGAAC[C/T]CTCATGCATTGCTGG | 9873 |
rs557983097 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930641 | TCCCAATTATTTGGG[A/G]GCCTGAGGCATAAGA | 9873 |
rs557991810 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990148 | GCACTTAATAAGTGT[C/T]AGGCTGTGAAGGAAA | 9873 |
rs558021425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130120 | ATCTCGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 9873 |
rs558025248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887847 | TAAGCTGAGACCATC[C/T]AATACTCAGATTAGT | 9873 |
rs558026250 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912146 | CTCTTTCTTTCTTTT[A/G]TCTGACTGCTGTAGC | 9873 |
rs558032326 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033746 | TCAACACTTGAGTTT[C/G]AGTACTGTACTGCCT | 9873 |
rs558036622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955285 | TTTTATTTATACTTA[C/T]TCATTTATTATAAAA | 9873 |
rs558043171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080278 | ATCCAGTCTGGGTGA[C/T]AGAGCAAGACCCTGT | 9873 |
rs558047144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988041 | ATAAACCGCGGAGCC[C/T]CTGAATTTTCACAAG | 9873 |
rs558051946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041415 | TGTTCTTTTTAATAA[A/T]CACCATTCTGACTGA | 9873 |
rs558064364 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033542 | AATGGAGGAATTATA[C/G]GGCGCTACACAAGAC | 9873 |
rs558067009 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904982 | TTTATTTATTTATTT[A/T]CTTGGGAAGGTAACG | 9873 |
rs558079954 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965525 | TTACATTTGTACATA[C/T]TGCCATTATAGTATT | 9873 |
rs558085027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983344 | GGCATGGTAGCATGC[A/C]CCTGGATCCCAGCTA | 9873 |
rs558095243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876187 | AATAAAATATTAGCT[A/G]GGTTTGGTGGTACAT | 9873 |
rs558095989 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063825 | AAGAGACTTAGACTC[C/T]CACACAATAATAATG | 9873 |
rs558098471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880869 | TGATACCCTGTCTCG[A/G]AAAAAAAAAAAAGAA | 9873 |
rs558099885 | snp | C/T | 1.66305e-05 | 0.00288357 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849734 | CAGAATTTAATAACA[C/T]TATGTTGGAGAAATA | 9873 |
rs558112889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034381 | TGATTTGACTTTGGT[A/G]GCACACAAACATGCA | 9873 |
rs558122899 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922230 | TGCGTGGGTTCTGAT[C/T]TTTGCTCATCTGCTT | 9873 |
rs558124282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105420 | CCCCAGAATCTACCA[A/G]GCTCTTTATTTGGTA | 9873 |
rs558131730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925250 | TTTTTGACCTTACCA[A/T]AATCAGGATCATTTC | 9873 |
rs558131993 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876965 | TGTCTAACAGTAATA[G/T]GATCACTTCATTTTT | 9873 |
rs558140383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881009 | TTAAGGCCACAGGCA[A/G]CAAAACAAAAAACAG | 9873 |
rs558144943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049274 | CATAGTAAAACTTTA[A/C]GGAAAAAATTAAAAC | 9873 |
rs558167408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996815 | TGCCAGCATTAAAGA[A/C]CACCACCACACACTG | 9873 |
rs558168291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916482 | CATGTCTGGCTAATT[A/T]AAAAAATTTTTTTGT | 9873 |
rs558177096 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867955 | GTTCATGGCACTCTT[C/T]AGCCATGTGTCCACA | 9873 |
rs558191190 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868907 | GTTACCTTTTTTTTT[A/T]AAATTTTTTATTTTT | 9873 |
rs558205382 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881864 | GTAGAGGCTGGGGCC[A/G]GGTGCGGTGGCTCAC | 9873 |
rs558231079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072699 | AAGATTGGCAGAAAG[A/G]AAAGCTCCAAATATA | 9873 |
rs558232612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883807 | CATGGTGGAGTGCGC[C/T]TGTATTCCCAGCTAC | 9873 |
rs558234788 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057259 | TAAGTGACCGGCATA[A/G]TACCTAGGACACAGT | 9873 |
rs558280662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064255 | AGAACAAAGACACAA[C/T]GTGCCAGAATCTCTG | 9873 |
rs558294398 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964536 | AGGGCAAGGGCTGTG[G/T]TTTTGTTGCCTTTTC | 9873 |
rs558296373 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067182 | AGTTCATGTCCTTTG[A/C]AGGGACATGGATGAA | 9873 |
rs558301508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119536 | GTGGCACAATTATAG[A/C]TCACTATAACCTCAA | 9873 |
rs558311681 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992016 | TTTAGAAAACCCCAT[C/T]GTCTCAGCCCAAAAT | 9873 |
rs558327491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911503 | AAATTTTAGGATTGC[C/T]TTTTCTATCTCTGTG | 9873 |
rs558328216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007381 | ATCCCAGCATTTTGG[G/T]AGGCTGAGGCAGAAG | 9873 |
rs558330130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015974 | ACTTAGAAAATCTCA[C/T]TTTTCCAAATGTAAA | 9873 |
rs558343715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057075 | GCGACAGAGCAAGAC[C/T]CCGACTCAAAAACTA | 9873 |
rs558361211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119039 | AGGCGCGGTGACTCA[C/T]GTCTGTAATCCTACC | 9873 |
rs558364765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905557 | ACTCATCATTTACGT[C/T]AGGTATTTCTCCCAA | 9873 |
rs558373929 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988695 | GATAAGCTTTCAAGT[A/C]TGTAAATACAATGTT | 9873 |
rs558393956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008223 | GCACACCTGTAATCC[A/C]AGCTACTCAGGAGGC | 9873 |
rs558425425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126443 | TGTGCTACAACCAAC[A/T]GGAAACCAATCACTT | 9873 |
rs558426506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060646 | CATCCCACTGAAAAC[A/G]CTTATGAATGAGAGA | 9873 |
rs558444318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901133 | ATCGTGGCTCACGTC[C/T]GTAATGCCAGCACTT | 9873 |
rs558449480 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888515 | AGGCAAAGAATGAGA[C/T]GGATATAGGTATCAA | 9873 |
rs558453984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107970 | TGGCAAGTGTATCTT[C/T]AGTTTTCTGAGTGAA | 9873 |
rs558459271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914252 | ACTCCTGACCTAAAG[C/T]GATCTGCCCACCGTG | 9873 |
rs558466117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045025 | CAGTGAGCCGAGATC[A/G]CTCCACTGCACTCCA | 9873 |
rs558479068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892989 | CTTTTTAAAATGCTG[A/G]CAAATTTATTTTTAT | 9873 |
rs558486927 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930784 | TATTCAGACTGACAT[A/G]ATTTTTTAATTTTTA | 9873 |
rs558496622 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908537 | CTCCACATCCTCACC[A/G]GCATCTGTGTTACTG | 9873 |
rs558504717 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097921 | TCAAGCGATCCTCCT[A/G]CCTCGGCCTCCAACT | 9873 |
rs558534324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038510 | ACAGCGTGGATACTA[C/T]GCAGCCATGAAAAGA | 9873 |
rs558563726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920390 | TCCAGGAAAATGTAA[A/G]TTACCCAAATATACT | 9873 |
rs558571052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853613 | AGAGATGGGGTTTTA[C/T]CGTGTTGCCCAGGCT | 9873 |
rs558572300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893679 | TAGGCGTGGTGGCGC[C/T]GGAGGTTGCAGTGAG | 9873 |
rs558578718 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930595 | ACCAAAAATACAAAA[A/T]TTAGCTGGGCGTGGT | 9873 |
rs558594086 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039136 | CGTGTATTCCAAATC[A/C]TATCTATTCCTAAGA | 9873 |
rs558599129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109117 | TTTATGCCAGTACCA[C/T]GCTGTTTTGTAGTAT | 9873 |
rs558602447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966921 | GTTAAGAAAGTGGCC[A/G]GGCGCGGTGGCTCAC | 9873 |
rs558607596 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993873 | GTAACTAACCTGCAC[A/G]TTGTGCACATGTACC | 9873 |
rs558618112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075834 | AAAATCATTAAACAC[A/G]GGGGCCAGGCATGGT | 9873 |
rs558622902 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913838 | CCAAAAAAAAAACAA[A/C]AAAAAAAACCCTAGA | 9873 |
rs558623543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054015 | AAAGGGGGGAAGAGT[C/T]CTCACAACAGATAGT | 9873 |
rs558641437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860714 | GCTGGGCGTGGTGGT[A/G]CTGGGAGGCTGAGGC | 9873 |
rs558653893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913146 | GGGAACTCCATCCCC[A/G]TGATTTAATTACCTC | 9873 |
rs558655428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032024 | TCATCAGTATGCTGC[A/G]ATGTTACACAATTAT | 9873 |
rs558660572 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065084 | GGCCAATATCCCTGA[G/T]GAACATCAATGCGAA | 9873 |
rs558665279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931205 | GTTCAAGTGATTCTC[C/T]TGGCTCAGCCTCCTG | 9873 |
rs558666358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000597 | AATTATTATACAAAA[C/T]GGGTCAAGTTGAAAG | 9873 |
rs558670908 | in-del | -/TGT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100332 | AAGCGCTTTACATGC[-/TGT]TTTTGTTGTTGTTGT | 9873 |
rs558677026 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088036 | AGGCACATGCCACCA[C/T]ATGTGGCTAATTATT | 9873 |
rs558686937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045360 | TGGAAGTCAGTGTGG[C/T]GATTCCTCAGGGATC | 9873 |
rs558698663 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119472 | TATGATGACAGATTT[A/G]TTTTTTAATACATAT | 9873 |
rs558704725 | snp | C/G | 9.82946e-05 | 0.00700982 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141824 | CGCGTACGCATCTCT[C/G]CGAACCCCAAAGCCC | 9873 |
rs558706522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907933 | TAAACTATTGCTGAC[A/G]TGGTCACCTTATTGT | 9873 |
rs558729368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993519 | CAACCCAAATGTCCA[A/G]CAATGATAGACTGGA | 9873 |
rs558732342 | in-del | -/A | 0.113334 | 0.209338 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983294 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAT | 9873 |
rs558733522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938789 | TTCAGTTCTAAACTA[C/T]TGAAAAAAATCTTAT | 9873 |
rs558744636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068121 | TCCCACCAGGTCCCT[C/T]GCACAACACATGGGA | 9873 |
rs558752961 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959183 | CAATCCTGGTTTCCC[C/T]GTTATTCTTTCTTTT | 9873 |
rs558759741 | in-del | -/AAC | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030020 | AAATGGCCAGTTTTT[-/AAC]AACAACAACAACAAC | 9873 |
rs558762565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069841 | CAAATAAAACATCTA[A/G]ATTCATAAATGATAC | 9873 |
rs558765297 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045883 | GTAACTAACCTGCAC[A/G]ATGTGCACATGTACC | 9873 |
rs558788656 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050190 | CAAATAGGTATGTCC[A/G]TGGTCTAACAAAACT | 9873 |
rs558789170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924175 | CAAACTTCTGGGTTC[C/T]AGTAATCCGCCTGTC | 9873 |
rs558818983 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070463 | CAGTCTCGTTCTGTC[A/G]CCCAGGCTGGAGTGC | 9873 |
rs558841621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944996 | TAAATTATAGATTCA[A/G]TGCCATCCTCATCAA | 9873 |
rs558872397 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908533 | TTTTCTCCACATCCT[C/T]ACCAGCATCTGTGTT | 9873 |
rs558881527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952223 | CCAGAAAGATATATA[C/T]GGCCTATGAAGGAAA | 9873 |
rs558896624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992114 | GCATTCTTATACACC[A/T]ATAACAGACAAACAG | 9873 |
rs558901959 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846175 | TAAGCTGCTCCTCCT[C/T]TTGCTCTTTTTTTTT | 9873 |
rs558928869 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060144 | TGTATAAGGAGTTAG[C/T]CACCCAATAGATTCA | 9873 |
rs558948624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933215 | GGTGGAGGTGGTCCC[C/T]TGACTTAAATTAGGT | 9873 |
rs558951503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885375 | TTGAGAATGTAGACT[C/T]AAATACTTGCATTAG | 9873 |
rs558957367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025462 | CATGCACACATAGAG[G/T]GGAACAACAGGCACT | 9873 |
rs558969458 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880401 | TATTGTCACAAATAC[A/G]GACACACAGACCAAT | 9873 |
rs558970325 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981613 | CTGTGCTAAAAATCA[C/T]CTTTAGTAAATGTGT | 9873 |
rs558973232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925484 | TGATCTATGATCGTG[C/T]CACTGCACCCCAGCC | 9873 |
rs558973976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093519 | AAGAGCTGTAATGCA[C/T]CCATTTAAATTCATC | 9873 |
rs558975973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101912 | GTCTATGTATGAAAA[C/T]AGATTTGCTTTCAAG | 9873 |
rs558988953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878023 | AAATATATAAAGCAA[A/C]TAAAATATTAGATAA | 9873 |
rs558991287 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141357 | CTATTCCAACTTCTT[C/T]TCGGCCGCCCCGTGG | 9873 |
rs559006881 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945646 | TATTTTTGCAATCTA[C/T]TCATCTGACAAAGGG | 9873 |
rs559015565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086270 | AAAAATTAGCTGGGC[A/G]TGGTGGTGCGTGCCT | 9873 |
rs559019164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984469 | CTTTGTAGATAACTT[A/T]AAAATATTTTGCCCA | 9873 |
rs559021788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017335 | ACTATAACAGGGCCT[A/G]ATGTAATGGTTATAG | 9873 |
rs559029921 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071650 | AGGCTGCAGTGAGCC[A/G]AGATCATGTCACTGC | 9873 |
rs559034253 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018705 | TGAATAAAAACTTCT[C/G/T]TGGTTCCTAATTTTC | 9873 |
rs559077590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839062 | GTTGTTCTCAATGAA[A/G]TATCAAGCCCACAAA | 9873 |
rs559078359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963319 | TGGCAAAGTAGTGAG[C/T]ATTTACTACGCACTA | 9873 |
rs559080403 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092714 | CAAGATCACAATCTA[C/G]ATCCACATGGACCAA | 9873 |
rs559082008 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077882 | TCAAATTATAAATTG[A/T]GTGGCTTATTGTGTA | 9873 |
rs559090808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072317 | CGAATAGCCATGAAA[A/C]AGTGAAACTTACTAG | 9873 |
rs559107823 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033787 | TTAGTTATGAGTATT[C/T]TTGGATAAGACACCA | 9873 |
rs559115604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979620 | AATGAAAGAGTTTTC[A/C]ACCTTTAATTCTATA | 9873 |
rs559117300 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918331 | TGTCATCTGCAAAGA[C/G]AGGTAATTTTAATTC | 9873 |
rs559133725 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986103 | AGAGAAAACATTCAG[A/G]GATGAACACATATGC | 9873 |
rs559148196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977338 | AATGGACAAATGGGA[C/T]CACATCAAGTTAAAA | 9873 |
rs559156587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064648 | ATATCCTTATATCAG[C/T]GGTGATATCCTGTGG | 9873 |
rs559166424 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121817 | ACATGGATTGCTGGG[C/G]TCCACTCTCAGAGTT | 9873 |
rs559199319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955586 | GGATCCCTTGGCAAC[C/T]AGCCCCCATCCTGAC | 9873 |
rs559219442 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862934 | TACATATATGATTAA[-/T]TTTTTTTTTAAAGAG | 9873 |
rs559226570 | in-del | -/AAC | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852965 | GGACACAAAGAGGGG[-/AAC]AACAGACACTGGGGC | 9873 |
rs559237194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978084 | CCAAACACCACATGT[A/T]CTCACTCATAGGTGG | 9873 |
rs559241386 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870415 | ATATCCTATATAACT[A/G]TGCTTCTACTTTTCC | 9873 |
rs559243105 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954865 | CTCAATGTGAATTGA[C/T]ATCTATACATATACA | 9873 |
rs559253461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862534 | TGACAAAGGATATGC[A/G]AGATCTATCTACTGA | 9873 |
rs559259050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910141 | AGGAGCACCTCTGCC[C/T]GGCTGCCCCATCTGG | 9873 |
rs559284359 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871123 | ACCATAAACAAGTAA[A/C]CACAGAACTAGTTTT | 9873 |
rs559286766 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989597 | GAACAAGAGAAGCAC[A/G]AAACCTGGGTACCAC | 9873 |
rs559287439 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128813 | TATCTTTGAGATTAA[C/T]TTCACGTTTCAACCC | 9873 |
rs559290845 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978891 | AGATGAAGTCTCACT[C/T]TGTCACCCAGGCTGG | 9873 |
rs559308407 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983963 | CAATAACAAGTATAT[G/T]CCAATGAGATGCAAC | 9873 |
rs559309566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73140997 | GGGTGAGTTAGGCGT[C/T]AGGCAAATGTTTGCC | 9873 |
rs559312868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117714 | GTAAAGAATTTTACA[A/G]CTAACATCCATATAG | 9873 |
rs559314663 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863104 | GTTGAAATTTTTTTT[A/C/T]TTCTTTTTTTAGAGA | 9873 |
rs559317989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105574 | CTAAGCCTCAATTTT[C/T]ACATCTACAAAATAT | 9873 |
rs559324258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949360 | GAGGCTGAGACAGGA[C/G]AATCACTTGAACCCT | 9873 |
rs559331945 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856429 | ACTGTTTGCCTAATA[A/C]AATTCTATAGCACTG | 9873 |
rs559347584 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028001 | AAACACCTGGATGTC[C/T]AGGCAGAAGTCTGCT | 9873 |
rs559349562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089117 | TTCACATAATAAATA[C/T]TTGGAAATCTATTCA | 9873 |
rs559374414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043259 | TGAGAGATTTTATCA[C/T]GAAGGAATTTTTACT | 9873 |
rs559380418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098111 | TTTCCTTTTGGGTTT[A/G]GCATGCTCTTTTCCT | 9873 |
rs559381126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987676 | ACCCTATCAAATCCC[C/T]ACTTCTCAGAAACGC | 9873 |
rs559383402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034517 | CTGAGCCTGTACCAA[C/G]GAAATAGAGATCAAA | 9873 |
rs559400311 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131441 | GGCTGAGGCAGGAGA[A/C]TGGCGTGAAACCAGA | 9873 |
rs559418791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843083 | TTATCCTACTGAAGG[C/G]TTACTCCAGGGCAAT | 9873 |
rs559422905 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989361 | CTGCTGATGACTGAC[A/G]TTAAGGTAAGACATG | 9873 |
rs559425460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003341 | TATGAAAATTCATGA[C/T]ACACAGATTCTTTTA | 9873 |
rs559430022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880376 | GACTTTAGTAACCAA[A/G]ACAGCATGGTATTGT | 9873 |
rs559436457 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975415 | AAAATTACAGTCAGA[A/T]AGAAGGAATACATTC | 9873 |
rs559441974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048634 | TCTTACAGTAAGTGC[C/T]GGAAGTACGAAAAAG | 9873 |
rs559444754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027693 | GGGCATTTCAGAGAT[A/G]TTCGCTGCACTCCCC | 9873 |
rs559451820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948582 | TATCAATTTACATTA[C/T]CAATAATAGAATATG | 9873 |
rs559454177 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892616 | TTGTTTTGTTTTTTG[-/T]TTTTTTGAGACAGAG | 9873 |
rs559468163 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909289 | TGATCTGCCCGCCTC[A/G]GCCTCCTGAGGTGCT | 9873 |
rs559468769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872898 | TGGCTTTATCATTTG[A/G]TCCCACCAGTAGGGT | 9873 |
rs559475396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917191 | GGTTTCACCATATTG[C/G]CCAGGCTGGTCTTGA | 9873 |
rs559477062 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863096 | CCTGGCTAGTTGAAA[-/T]TTTTTTTTTTCTTTT | 9873 |
rs559486754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996301 | TAATACTTAAATACT[A/G]TCAGGGTTGTGTAAA | 9873 |
rs559490789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941507 | ACTTATTATTACTTT[A/G]TCATTAACTGTTTTG | 9873 |
rs559510801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990064 | GTTAAGAAAGGACTA[A/C]AGGGGATGAGACATC | 9873 |
rs559510810 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981160 | GTACAGTACATGAAA[A/G]CTGAAAGTATGTTTT | 9873 |
rs559513005 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845331 | GAGGCTGAGGTGGGA[C/G]GATCACTTGAATCAG | 9873 |
rs559517131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889020 | AGTGCAGTGGCGTGA[C/T]CTCAGCTCACTGCAA | 9873 |
rs559523374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850493 | CGAGTAGCTGGGACT[A/G]CAGGTGCCCACCACC | 9873 |
rs559538179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018975 | ATAACTCATTATCTG[C/T]AGAGAAGAATAACAA | 9873 |
rs559546315 | in-del | -/AAG | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059383 | AGGTTTTCTAGGATT[-/AAG]AAGTTGTAGGACGGG | 9873 |
rs559562008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874901 | AACTTGATGGCATTC[C/T]AGATACTACTTGACC | 9873 |
rs559573440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139423 | GTGGTATTTCTTTCA[G/T]TAAAATAAGTCATCC | 9873 |
rs559590856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117096 | TATTTTTGTTTTCCA[C/T]TCATCTTTCTACTTA | 9873 |
rs559598772 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019751 | AGGTCCTAAATAATA[C/T]TGCACATTTCTGAAA | 9873 |
rs559653304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124337 | ATGGGTGCAGCACAC[C/T]AATATGGCACATGTA | 9873 |
rs559657264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058004 | CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGACTA | 9873 |
rs559658569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011773 | GGGTCTCTCTTGGCT[C/G]CTGACTAATCCCACC | 9873 |
rs559690928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959988 | AGGAAGAAACCTACA[C/T]ACTTCAAACACATAT | 9873 |
rs559693369 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081872 | GGATTCAATAAATGT[A/C]AGCTATCATTACTAG | 9873 |
rs559695752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004192 | ACATGGTAAGTACTA[C/T]GTTATGTATTTTACA | 9873 |
rs559696351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028275 | CTTAAGGCCTTGGGA[A/G]CCCACATCTTGCAAC | 9873 |
rs559697641 | in-del | -/AAAATAAAAT | 0.00914312 | 0.0669923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080960 | CTCAAAAAAACAACA[-/AAAATAAAAT]AAAATAAAATAAAAT | 9873 |
rs559709560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935796 | TCAGGTTACTTCATG[A/T]TCTGTGAAAGAGGAA | 9873 |
rs559714644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049467 | GAAAGACTGGGAATG[A/G]GATGTAGACTACTAG | 9873 |
rs559716011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100254 | CTTCCTCCCTTCTCA[A/G]GAAAACCCTTCTCCT | 9873 |
rs559721202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012932 | ACAACTTGATTTCTG[C/T]TACAATTTCCTTGGT | 9873 |
rs559737261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882578 | ATAAATGTCTGAGGT[C/G]ATAGATATCTTAATT | 9873 |
rs559737476 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129027 | CAGGCATGTGCCACC[A/G]TGCCTGGCTAATTTT | 9873 |
rs559756589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854025 | CACAATGAGATACCA[C/T]TTCACACCCATTAGG | 9873 |
rs559756707 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845770 | TTCCCTCTTTCCTAT[A/C]TGATGAGCAGACTTA | 9873 |
rs559756810 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906476 | TGCCATTGCTTTCGG[C/T]GTTTTAGTCATGAAG | 9873 |
rs559757743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918395 | TTCTTACCGAATTGC[C/T]CTGTCTAGGACTTCC | 9873 |
rs559768272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846347 | CACCATGCCTGGCTA[A/C]TTTTTTGTATTTTTA | 9873 |
rs559771047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905660 | GTTCTCATTGTTCAA[C/T]TCCCATCTATGAGTG | 9873 |
rs559774641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991682 | TTATCTCAATAGATG[C/T]AGAAAAGGCCTTTGA | 9873 |
rs559792850 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109699 | GCTCTTTCTTTCTCT[C/T]GTCTGACTGCTCTTG | 9873 |
rs559815778 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889463 | CACTGCTGAGTGTTG[A/C]GAAAGTACAGAAAAA | 9873 |
rs559827873 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944584 | GAAATAAAGAGTATT[C/T]AATTAGGAAAAGAGG | 9873 |
rs559866459 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042240 | GAGATTATTTTTAAA[C/T]TCTGGTGAAAGACAG | 9873 |
rs559879763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091471 | GGAGAATCACTTGAA[A/C]CCGGGAGGCAGAGGT | 9873 |
rs559884681 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117309 | GAAGTGGAGAACTAA[A/G]AATTCACAATCAGGC | 9873 |
rs559887012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008395 | TAATTTATATAATAA[C/T]TAGTAACAAGAAGAA | 9873 |
rs559898467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993833 | TTACTGGGTGCAGCA[C/T]ACCAACATGGCACTG | 9873 |
rs559903312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952565 | CCTGACCTCAAGTGA[C/T]CTACCGGCCTCGGCC | 9873 |
rs559906939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984915 | CAAAACCCCCATGAA[C/T]TGGGAGGGAAAGTTC | 9873 |
rs559907706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941059 | GCTATTGGTGGTTCT[C/T]GCCGGGCAGCTTAGA | 9873 |
rs559930173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042987 | CTATATATGAGGTCA[C/T]GTCATCTGCAAAGAA | 9873 |
rs559940860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083172 | AATACTTTACAAATA[C/T]AGTAAATAATGTCTC | 9873 |
rs559945689 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986038 | AGCAGTTAGTCTTTG[A/C]AAAGCCAGTGTGAAG | 9873 |
rs559946068 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867495 | GTGCAAATCTCTGGA[C/T]GTTTATTTTCATTTT | 9873 |
rs559952060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000208 | AATTAGAATCAAAAC[A/G]CTGGATGGCTTCTAA | 9873 |
rs559953086 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879911 | GACTGAGGCCGAACA[A/G]TCGGTTGAACCCAGG | 9873 |
rs559958964 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054754 | AATCATGGCTCACTG[A/C]AGCCTTGACCTCCTG | 9873 |
rs559963437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028848 | CCCTTTCGTTCTCTC[C/T]GTCTCTCCTGCCACC | 9873 |
rs559973588 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123227 | CTGACATTTTTGACC[C/T]ATGACAAATTCAATG | 9873 |
rs559988151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870066 | CCATCATGTGCTTGC[A/G]TGCCTGTGTGCGTGC | 9873 |
rs559988585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945407 | ATTAATTCAAGATGG[A/G]TTAAAGACTTAAATG | 9873 |
rs559993622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035959 | CTCTTGACCTTGTGA[C/T]CCGCCTACCTCAGCC | 9873 |
rs560004633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893295 | AGCATGAGCCTCCAC[A/G]CCTGGCCTAGATCAT | 9873 |
rs560009035 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903535 | GGAATTTCTATAAAA[C/G]GAGAATTCTGATAAG | 9873 |
rs560009367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973310 | AGGCAGAGGTTGTGG[C/T]GAGACGAGATCGTGC | 9873 |
rs560012099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927415 | ATGGTGTCAGTGTAG[C/G]TTCATCAATTGCAAC | 9873 |
rs560023098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021620 | GGTACTAGGCTTAAT[A/C]CCTGGGTAACGAAAT | 9873 |
rs560024145 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088205 | CCATATTTTTGTTGT[A/G]TCTTTCCTACATTTA | 9873 |
rs560035104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135558 | GTATGTAGAAACTTA[C/T]TGTAAGTGGTCTTAA | 9873 |
rs560042934 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896581 | CTGCCAAGAAGGCCG[C/T]TGATGAGATCCTCTT | 9873 |
rs560060676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025046 | CACTGTTTATGGAAG[C/T]GTAAATTAGCTCAGG | 9873 |
rs560073516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094521 | AGTTGTCCATCAATG[A/G]GATCATGGATAAACA | 9873 |
rs560081132 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967127 | ATGGCGTGAACCCGG[A/G]AGGCAGAGCTTGCAG | 9873 |
rs560086430 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085608 | AAAAGTCACCACACA[A/G]ACCCACGGGAAGGTG | 9873 |
rs560086840 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035233 | GGTCTCGCTCTGTCA[C/T]CCAGGTTGGAGCGCA | 9873 |
rs560088509 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001592 | TACTGAGATACAAGA[C/T]GAAGATTGGGTACCT | 9873 |
rs560089565 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999383 | GGAGGGCAGTGGCAC[G/T]ATCTCAGCTCACTGC | 9873 |
rs560100346 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143026 | GCGCGAGAGAGGCGA[A/G]CAAGGACAAGTCGCT | 9873 |
rs560101000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870672 | TTGGGAAGCCGAGGG[A/G]GGCAGATCACGAGGT | 9873 |
rs560101355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074277 | TTTCAGTTGAGGAAG[A/C]ACAAAATATGCTTGC | 9873 |
rs560110869 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933042 | GTAGTGGCATCCTTT[C/T]ATGTGGAATTCCAAG | 9873 |
rs560120347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892508 | GCCCAGGCTATTAAA[C/T]AATACACAGAGAAAT | 9873 |
rs560124503 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112518 | GCTTCTTATACTTGA[A/C]TACTGATAGCTTTCC | 9873 |
rs560126005 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062506 | CAAGCTAAAGGAGCA[C/T]GTTCTAACCCAATGC | 9873 |
rs560158842 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052717 | ATATTCGGTATTTTT[A/T]ATAATCTTCATACTT | 9873 |
rs560169547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032356 | ACCTCGGCTTCCCAA[G/T]AAACTAATATTACAG | 9873 |
rs560176571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909233 | GTGGAGACGGGGTTT[C/T]GCCCTGTTGACCGGG | 9873 |
rs560208078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884501 | TCTGTGTGTATGTTA[C/T]ATATATCATATATAT | 9873 |
rs560210523 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865121 | AGTTGCACTATTAAT[G/T]TCTAACAGTAGTATT | 9873 |
rs560216114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901288 | TGTGGCCCCAGCTAA[C/T]CGGGAGGCTGATGTG | 9873 |
rs560218397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093753 | ATTACAGGCATGCAC[A/C]ACCATGCCGAGCTAA | 9873 |
rs560222069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044759 | AACATTCTAGCATGT[C/T]ATATAAAAATCATCT | 9873 |
rs560223559 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995831 | CCTGGGCCAACACAT[C/T]GAAGTCCTACAAATG | 9873 |
rs560252742 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007573 | GCCACTTCACTCCAG[C/T]TTGGGTGCAAAAGTG | 9873 |
rs560264936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915607 | GTGGATCACCTGAGG[C/T]CAGGAGTTCAAAACC | 9873 |
rs560276943 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107034 | TTTTTTGTTAGAAAA[G/T]CTATATATATATATA | 9873 |
rs560281769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086045 | AGAAAACTATGTGCG[A/G]GCAAAATGTAAATAT | 9873 |
rs560284450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045147 | GAAGACATTTATGCA[A/G]CCAAAAAACACATGA | 9873 |
rs560301779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903310 | CAAGCTCCGCCTCCC[A/G]GGTTCATGCCATTCT | 9873 |
rs560305262 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888994 | CAGAGTCTCGCTGTC[A/G]CCCAGGTTGGAGTGC | 9873 |
rs560315460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112149 | CTGATTAAAGAACTC[C/T]CTTTAGCATTTCTTA | 9873 |
rs560324591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976700 | GTACTGGCATAAAAA[C/T]AGACTCACAGACCAA | 9873 |
rs560327115 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938110 | GGCAGAATTTAGTTA[A/C]CTGAGGTAAATAAAT | 9873 |
rs560332442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046775 | TTGATTAAGACAGGG[A/G]TTTCACCATGTTGCC | 9873 |
rs560334038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862866 | TGCAATACCGGCATC[A/C]AGCTGGACAAACAGA | 9873 |
rs560335201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886108 | GGGTGTTAGAAAACC[A/G]TTAGTTTAGTTTAAA | 9873 |
rs560344203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854943 | AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGT | 9873 |
rs560346601 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923037 | TCATATAAATCAAAT[A/C]ATATAATATATGACT | 9873 |
rs560355657 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932507 | CGTATTACACCTTCT[C/G]TACAATGCAGTTTTT | 9873 |
rs560374168 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979249 | AAACAGAACTCTCAT[A/G]CATTAAAACTACTAT | 9873 |
rs560376787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119194 | GTAGTCCCAGCTACT[C/T]GGGAGACTGAAGAGG | 9873 |
rs560377115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062664 | TTTCAATAGCCAAAT[C/T]GATCAAGAGGAAGAA | 9873 |
rs560413081 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869708 | AATATAACTTGTGAA[A/G]AGGAAGAGATCAAGA | 9873 |
rs560413103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930808 | ATTTTTAAAGGGTAG[C/T]AGGGGTTGAGGAGGA | 9873 |
rs560414374 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968070 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCT | 9873 |
rs560414917 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969739 | CAGAAATTATAAAGC[C/T]ATGTCTGAAAATAGA | 9873 |
rs560415930 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963113 | TTAGATCAGTGCCTA[A/G]CATATACTCAGTACT | 9873 |
rs560432308 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870009 | TTCTTTCCACACCCC[C/G]CTATGCTCCCACCCC | 9873 |
rs560433670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077387 | CATCTATCACAATAT[C/T]AAAAATTAAGAAGAC | 9873 |
rs560434676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914766 | TTAAATGTAAAACCC[A/G]AAACTATAAAAACCC | 9873 |
rs560438182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055312 | CACCCCACTGGACTC[C/T]AGCCTGGGCAACAGA | 9873 |
rs560449733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931544 | GGCCAAGGCAGGTGG[A/T]TCACAAGGTCAGGAG | 9873 |
rs560467603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078287 | AAAACTGGCTGTATC[C/T]ACTAAAGTAGAACAT | 9873 |
rs560472705 | snp | C/T | | | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836626 | GGATTAATTTACTTT[C/T]TCCTCTCTCTGTCTG | 9873 |
rs560483366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070156 | CAAAGATGTTCCTAG[A/C]CTTCATATAATGGTC | 9873 |
rs560499436 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894828 | TTTCATATATACATA[A/T]ATGAATGAAAATATT | 9873 |
rs560505551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112752 | CTCCCAAGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 9873 |
rs560512458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961198 | AATCCAGGTGTTTCT[A/C]GGTCATTTTGAATTG | 9873 |
rs560518729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002058 | AGATTATAATATTCA[C/T]CTCCTGAGATTTCCC | 9873 |
rs560544711 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025680 | ATAGAATTTTAAAAA[A/T]TTTTTAAATCTCCTT | 9873 |
rs560546086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953480 | AATTTACAGCTATAT[A/G]AAAGATACTGCTAAT | 9873 |
rs560547166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962026 | ATTGAAACCTAAGAA[C/T]TCCATTGAAATATTC | 9873 |
rs560552838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895402 | CAAAAATGGCATAAA[A/T]ACCTTGCGTCTAACA | 9873 |
rs560557945 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020639 | TTTAAAATATTCTTC[A/G]TTGTTCTGTGTGGTA | 9873 |
rs560558127 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956026 | TAGTTGATTCCAGAA[C/T]TGGGGCAAAGAAAGT | 9873 |
rs560562232 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002690 | TCTCTCAGTGTAACA[A/C]CCTCTTCTCTTTATC | 9873 |
rs560566532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062206 | AACTTCAGCAGACCT[G/T]CAGCAGAGGGGCCTG | 9873 |
rs560592321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847492 | AACTTCTCCCTTCAT[A/G]GACCTTTAGCGGGGA | 9873 |
rs560596203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863474 | TACCACACCAAAAAT[A/G]TGATCCATAAAAGAA | 9873 |
rs560611476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940045 | AGTGTTACAGCCTGT[A/G]TAGAAAATGCAAGCA | 9873 |
rs560617999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911899 | TCCTATGTATTTTAA[C/T]GTATTTGTAGCTATT | 9873 |
rs560621840 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126787 | TCACGTCTGTAATCC[C/G]AGCACTTTGGGAGGC | 9873 |
rs560624496 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037850 | CAAACATAGTGGACA[A/G]CTTTAGGAAAAGAAG | 9873 |
rs560641392 | in-del | -/T | 0.26326 | 0.249648 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100863 | TGCTTCTACGTGGGA[-/T]TTTTTTTTTTTTTCC | 9873 |
rs560652970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912683 | CTATTTTTTGGAATT[A/G]GTTGAGTAAAATTGG | 9873 |
rs560654777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905789 | CTTTTTATGGCTGCA[G/T]AGTATTCCATGGTGT | 9873 |
rs560659458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855594 | ATATTTTACCATACA[C/T]ACGAACAAACGTGAA | 9873 |
rs560672684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127631 | CCATCAACTTACAGG[C/G]CTCCTCAGATAAACA | 9873 |
rs560674816 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121178 | ACACATACACATACA[C/T]ACACACACACACACG | 9873 |
rs560684304 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066776 | TGCAAATCAAAACCA[A/C]AATGAGATATTATCT | 9873 |
rs560686309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125897 | CAAACCATTCTTCCA[C/T]GGAGAGAGCTGGCTA | 9873 |
rs560693556 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142152 | GAAGGAGGCGGAGAC[A/G]GCGAGGGGGCGGGGG | 9873 |
rs560700574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946045 | GCCATTCCATTACCG[A/G]GTATATACTCAAAGG | 9873 |
rs560702953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848240 | CCAAGGCCCTTTACT[A/G]TCTGACAACAAACAC | 9873 |
rs560721700 | in-del | -/TTTGGGTTGGG | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127842 | CTGTAATCCCAACAC[-/TTTGGGTTGGG]GGGCGGGGGTGGGAA | 9873 |
rs560727350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994503 | GCAAGGATGTGATGA[C/T]ACCATTTACTATGGA | 9873 |
rs560733171 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943011 | GACTTTTTCTTTTGA[A/G]ACAGAGTTTTGCTCT | 9873 |
rs560739399 | snp | C/T | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144088 | CAATTTATTGTGAAG[C/T]GTTGAGCTAGTCAAT | 9873 |
rs560747602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134048 | ATCATATATGATATA[C/G]AGTCACATCATGTAA | 9873 |
rs560767483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056343 | CAAATTGCTAATTGA[G/T]GTACAGGAGTTATTT | 9873 |
rs560770261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986855 | CAAACACTACACAAA[C/T]AATGAACTATACCGC | 9873 |
rs560777228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051140 | GGGCTAACAAAGTGA[A/G]ACCCTGTCTCTACCA | 9873 |
rs560782632 | snp | A/G | 1.7894e-05 | 0.0029911 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840990 | AAAGAAGCTCATTTT[A/G]CTTGAGTTGTTGAGC | 9873 |
rs560790418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013096 | TCAACACCTCCATTA[C/T]GTTCTGAATAAAAAA | 9873 |
rs560792460 | in-del | -/AAAC | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837231 | GTTAAGAAGTGTAAA[-/AAAC]AACAACGAAAAAAAA | 9873 |
rs560795871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095916 | GCTGAGGATTAAAAA[A/C]AAAAAAAGTTATGCA | 9873 |
rs560838602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947253 | AAACTTCCCCTGGGT[A/G]AGAAATGCTGTGTGT | 9873 |
rs560841195 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051747 | AAACAACAAAAAAAA[A/T]TTGAAATAAATAGTA | 9873 |
rs560845342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043217 | CCTTTATTTTGCTGA[C/G]GTATGTTCTTTCTAT | 9873 |
rs560857746 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020235 | CAAAGAGAGCCACTG[C/T]TGAGTAGACACTAGG | 9873 |
rs560859392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087736 | TTTTTAAAATAAATT[G/T]AGTGCAGCCTAAGTG | 9873 |
rs560883549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033243 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 9873 |
rs560900003 | snp | A/C | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972003 | CAAAACTCAACCAAC[A/C]CTATTTTAAAATAGA | 9873 |
rs560901784 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874684 | AAGATTTTGTCAGTA[A/T]TTTATCAAACAACAG | 9873 |
rs560907900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074141 | TAAAAAGTCCAGAAA[C/T]AGACTTACATACACA | 9873 |
rs560915326 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897985 | ACTTTAGAAATCAGT[A/T]ACTCTCTTATGGAAA | 9873 |
rs560928361 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858125 | CGAGGAAGGGAGAAT[C/G]CAGATAAAGAATCTG | 9873 |
rs560940923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866362 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC | 9873 |
rs560995084 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084445 | GCCTAGGCTTGAGTG[C/T]GGCGGTGAGGTCCTA | 9873 |
rs561037621 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957394 | CTGCATAGTATTCCA[C/T]GGTGTATATGTGCCA | 9873 |
rs561053497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927334 | TCATTATACATTTGT[C/T]TAAACTGAGAATGTA | 9873 |
rs561053900 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096189 | AAAAAAATGCTGTCA[C/T]GAAAGAGATAATATG | 9873 |
rs561054838 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894380 | TAGACCCCAGCTCTT[-/A]AAAAAAAATTAGCAC | 9873 |
rs561056335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075292 | TATGACACAACAATT[A/C]CATTCCTTAGGTAAA | 9873 |
rs561062913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106475 | GCTCTTAAATCAGTA[C/T]TCTGCTTGTTAAAGA | 9873 |
rs561080298 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890788 | GTTAAATGTTACAAC[C/G/T]TTAATTGACCGATTC | 9873 |
rs561100237 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966265 | CCCGGGTTCATGCAA[G/T]TCTCCTGTCTCAGCC | 9873 |
rs561105350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851492 | ATTCCTGTAATCCCA[C/G]CACTTTGGGAGGCCG | 9873 |
rs561108011 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973096 | AGTTATGGCCGGGCG[C/T]GGTGGCTCATGCCTA | 9873 |
rs561120127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982150 | AAAGGGGATTTCAGG[C/T]AGTGAACAAAAAGGA | 9873 |
rs561124983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075974 | AAACACAAAAATTAG[C/T]CAGGCATGGTGGTGC | 9873 |
rs561148169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950383 | GCTTGTGTTTTTGGT[A/G]ATATCTGAGAAACTG | 9873 |
rs561156974 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837009 | AATAACCCTTTGAGG[C/T]TGTGGAAAACCCAAA | 9873 |
rs561164090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898798 | GCAGTGGTGTGATCA[C/T]GGCTCATTGCAACCT | 9873 |
rs561171172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990291 | TCAGCTGTGTTATTA[A/G]GCAACATTGCTTACA | 9873 |
rs561179258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844588 | GGGGCTGGAAAGTCC[A/G]TGTGGCTTTGCTTCC | 9873 |
rs561187303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998489 | AGAGGTTGCTGTGAG[C/T]GAGATCATGCCACTG | 9873 |
rs561188677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72844017 | TGTCTCTAAAAAAAC[A/G]AACAAAAAAAGAGAG | 9873 |
rs561189731 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000856 | ACATGTTGAAATCAG[A/G]AAATCCTAGTAAAAT | 9873 |
rs561201174 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021234 | ATCAAACATAGAATA[-/A]AAAAAAAAAAAAAAC | 9873 |
rs561214313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125827 | AACAATTTCAATTGA[A/T]TCAATGTAACTAAGA | 9873 |
rs561217899 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882923 | CTATCTGATTTCAAG[A/T]CTTACAATGTCATTA | 9873 |
rs561229973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959379 | GGACTACAGGCGCCC[A/G]CCACCATGCCCGGCT | 9873 |
rs561233301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943205 | CCCATGTTAGCCAGG[A/C]TGGTCTCGAACTCCT | 9873 |
rs561245359 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979907 | GACAGTCATAATGAG[A/G]GTTGTTATCACCAAG | 9873 |
rs561248575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990874 | AGAACAGAACTGAAC[A/G]AAATAGAGACACAAA | 9873 |
rs561251597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890132 | GATCAGCATAAAACC[A/C]TTAAAGACCATAAGC | 9873 |
rs561259922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099384 | ACCTGCTACAGAAAA[A/C]AGCTTGGCAGTTCCT | 9873 |
rs561270621 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936493 | AAACTCAAGAATCTC[A/G]ACCAGGTGCCATGGC | 9873 |
rs561282060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975261 | CTTAGCTATTGTGAA[C/T]AGTGCTATAAGACAT | 9873 |
rs561293871 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114877 | AGCTACAAGCTGTGC[A/G]CCCAAAACTGAGGGA | 9873 |
rs561295928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067168 | CATAAAAAAGGATGA[C/G]TTCATGTCCTTTGCA | 9873 |
rs561308972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046653 | AATATAGATAGACTT[C/T]GCTTACAAGGAAGCC | 9873 |
rs561320817 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092191 | GGAGTACATTGGTGC[A/G]ATCATAGCTCACAGC | 9873 |
rs561323609 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060754 | AAGCAAAGCTGTGGG[C/G]AAGATTGAAGTTAGA | 9873 |
rs561323820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869246 | TTGTTTATATCCCTA[A/T]CAAAAAAAGGAAATC | 9873 |
rs561344003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876575 | TAAACTTATTGAAAC[A/C]GGTTTATGGTCCAGT | 9873 |
rs561355327 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984818 | CTAAAGACAACAGGC[-/T]GCCTAAGCAGGTAAG | 9873 |
rs561364903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982978 | CCAGCCTGGTCAACA[C/T]AGCAAGACTCTTGTT | 9873 |
rs561379194 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970162 | AGAAAACTCACTAAA[A/G]CCACAAATGGCTAAG | 9873 |
rs561384579 | in-del | -/CAAAGAC | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084929 | ATCACTGCACCAGTG[-/CAAAGAC]CAAAGACATAAGAGT | 9873 |
rs561386570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860939 | GTTTAGCACTTAATG[C/T]CAATATTCAAAAAGA | 9873 |
rs561398103 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070107 | TTATCAGTAACAAGA[A/C]TTTCATTGTCCCAAG | 9873 |
rs561413558 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837874 | AAAATAATGCCGGGG[C/T]GTCCCCAGTAGAGAA | 9873 |
rs561416295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029552 | ATGGGAGCCAGGATG[A/G]GCAAATGGGACCCTA | 9873 |
rs561429507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877075 | CTCCAGGCTGCCTCC[A/G]GTGCAGCCTCATCCT | 9873 |
rs561440629 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008600 | GGATGAAAGCAGAAA[C/T]GGCCAGAGGTAAGTA | 9873 |
rs561450860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974477 | ACTTTAGAGGACACA[C/T]TCAAACCATAACAAG | 9873 |
rs561463756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079432 | CTCGAACTCCTGATG[A/T]CGTGATCCGCCCGCT | 9873 |
rs561481608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141415 | GCTAGAAACAAATCC[C/G]CCGCAAATTTGCAAA | 9873 |
rs561482772 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124915 | AGAAAAAAGCTATTA[A/G]AGCAAGGGAAAGCAC | 9873 |
rs561489019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077944 | AGTCAGTATAGTAGA[C/T]TCCTTGAGTAAGAGT | 9873 |
rs561491163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116161 | TGAATCTTTACTGAG[A/G]TGATCTTATGGTTCT | 9873 |
rs561526540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080370 | GACTTTAACTTTGAC[C/T]ACTCTGTAAAATGTA | 9873 |
rs561527066 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016236 | TGAATCCAGGAGGCG[A/G]AGGCTGCAGTGAGCC | 9873 |
rs561529845 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868555 | AATTAGCTAGGCATG[A/G]TATCATGGGCCTGTA | 9873 |
rs561537565 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110622 | TTTCACAAAACCAAC[C/T]TTTCATTTTGTTGGT | 9873 |
rs561541889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140831 | GCCCGCCAGGCCGGG[G/T]CCCCAGGGTTCGAAG | 9873 |
rs561553137 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919125 | ATAATAATATAAAAT[-/A]AAAAAAATCTAAAAA | 9873 |
rs561553907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040277 | GAGAAGCCCTCCTAC[C/T]AGAAGCTGTAATTGT | 9873 |
rs561571912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067797 | TTTCACATGAAATCA[C/T]TGAGAACAGTCTTAC | 9873 |
rs561577707 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860288 | CCAACCTGACTTAAT[A/T]GACATTTATAGAACA | 9873 |
rs561586379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932527 | ATGCAGTTTTTGGCT[C/T]CTCCAATACTCCTTT | 9873 |
rs561591740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970559 | CTCACTTAAAAACTA[C/T]TGCTAGCACTCTCAT | 9873 |
rs561593891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962309 | CGCTCTGACAGCTAA[C/T]GAAATCTGTACTTGG | 9873 |
rs561622547 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135593 | CAAAGAGAAAAAAAT[A/G]TAATAATAAACTAAA | 9873 |
rs561630032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963143 | TTTACGTGTGTTTTT[A/T]AAAAAATATTGTCTT | 9873 |
rs561646856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994413 | TAGCAGCAGCAGCAG[C/T]AGTAGTAGTAGCAGT | 9873 |
rs561674518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924472 | TATTTTCAGTAGAGA[C/T]GGGGTTTCACCGTGT | 9873 |
rs561675633 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888746 | CAACCTTAGCCTCCC[A/G]AATAGGTGGGAAGAT | 9873 |
rs561684116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111179 | TGTTCTGTAACTACC[A/G]GGTCCATTCGGTCTA | 9873 |
rs561685406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039443 | GACTCGCTTGAACCC[A/G]GGAGATGGAGGTAGC | 9873 |
rs561686408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121625 | CTTAAGACAATAAAG[G/T]CTTAACAAAGAATCA | 9873 |
rs561691917 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101197 | CATGACATTTATTCA[C/T]AAAAAGGCCACATAA | 9873 |
rs561692717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871921 | ATTTCCCTCCGAATT[C/T]TCTGCTTGGGGAGTT | 9873 |
rs561703510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878932 | GCCAACATGGTGAAA[C/T]CCCGTCTCTACTAAA | 9873 |
rs561716891 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032476 | AGTGATTCTCCCGAC[C/T]TGGCATCCCAAGGTG | 9873 |
rs561720119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986240 | TTAGAGACGGAGTCT[C/T]GCTCTGTTGCCCAGG | 9873 |
rs561723274 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928733 | TTTTTTATTTTATTA[C/T]TATTATACTTTAAGT | 9873 |
rs561724159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895211 | CTGGTGTGGACTGAG[C/T]CTTGGGACAATTCTG | 9873 |
rs561730331 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138432 | AAATTATTACAACTA[C/T]TGACCACCCATACCC | 9873 |
rs561732240 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031473 | AAGACCCTGTCTCCG[-/A]AAAAAAAAGAGAGAC | 9873 |
rs561735930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863620 | AAAGGATTTGTATTC[A/G]GAGTATAAACTCTTA | 9873 |
rs561744824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931825 | CAAACATCTGTCAAA[C/T]AGAATTGCACAGACA | 9873 |
rs561745461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104302 | GACAGAGTCTCACTC[C/T]GTTGCCCAGGCTGGA | 9873 |
rs561751818 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033138 | CTAAAAATATAAAAA[A/G]TTAGCTGGGCATGGT | 9873 |
rs561780008 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061600 | CAGCAGTCTGAGATC[A/G]ACCTGGGACGCTCGA | 9873 |
rs561786714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924574 | GACATGAGCCACCAC[A/G]CCCCACCCAGCTATT | 9873 |
rs561800757 | snp | A/C/G | 4.98694e-05 | 0.00499326 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849917 | AGAAACCATTGGCTA[A/C/G]TTTCCTTACTTCAAG | 9873 |
rs561802600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995173 | TTCATTCCTTTTTAT[C/T]GCCGAATAGTATTTT | 9873 |
rs561810419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122498 | TTGATCTGCTCTTCA[A/G]AACACAGGAATGGCT | 9873 |
rs561812960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025952 | ACTAAAAAACACAGA[C/T]ATGCTCCATGTTTTG | 9873 |
rs561816780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130178 | CGCGCCTGGCCCATA[A/G]TCTCTTATATTTATA | 9873 |
rs561837221 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041035 | GACCTCCAGTTCCAT[A/C]CATGTTGCTATAAAT | 9873 |
rs561860830 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888407 | GGGAAGGAAAGGACA[C/G]GAAAGCTCAAATGTA | 9873 |
rs561866636 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010937 | TGATGGGATAATCTT[C/T]TGGGTCTTGAGCAGT | 9873 |
rs561870324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033676 | CTATGGAATTCTATA[C/T]AAATTTATATAATTT | 9873 |
rs561873753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026887 | ACCATGTAAGACATG[C/G]CTTGCTTTCCCTTTG | 9873 |
rs561877607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137930 | ACCTTTATCCAGAAG[G/T]CCACAGAGGAGTGAT | 9873 |
rs561880510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979232 | TGGTAAGGATGTGGA[A/G]AAAACAGAACTCTCA | 9873 |
rs561881772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129884 | AATCTTTTTTTTTTT[C/T]TTTTTTTTGAGACAG | 9873 |
rs561897864 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072909 | TAAAAATAGCAAAAA[A/G]TTTTAGGTGCAACAG | 9873 |
rs561901278 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071103 | TAAAAGATGGTCTAC[C/G]AATTATTTTACAAGA | 9873 |
rs561901396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925261 | ACCATAATCAGGATC[A/C]TTTCTGATTATAGAT | 9873 |
rs561909510 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954951 | GATAGGAAAAAACTG[A/C]AGTGCTTTTTCTACC | 9873 |
rs561927506 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904118 | TTAATCCAGGCCGAT[A/G]ATGGGGTGAGATGAG | 9873 |
rs561930730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909788 | GGGAACTGAGGAGCA[C/T]CTCTGCCCGGCCGCC | 9873 |
rs561932617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916594 | TATTGGGATTACAAG[C/T]GTGAGCCACTGTGCC | 9873 |
rs561936599 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144010 | GCCCTGACAGCTGCG[C/G]GGTGGCAGCTAGAGC | 9873 |
rs561939918 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988385 | TCTTTTCCTACTTAT[C/T]CTTAAAAAAAGGTCT | 9873 |
rs561944189 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137325 | AAGAACACACTAACT[C/G]CTTTAAAAAAAACCT | 9873 |
rs561951069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947637 | TCCCATCCTCCAGCA[C/T]ATTCTGTTGGAACAG | 9873 |
rs561964692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872549 | AAACAATATAATACA[C/T]GGTCTTTTATGACTA | 9873 |
rs561977608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989211 | ATCCAGGGGAAAAGT[C/G]AGTACGTTCAGTGTC | 9873 |
rs561981817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881259 | ACATAATGGCCAACA[A/G]GTATATGAAAAAATA | 9873 |
rs562009294 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956205 | CCATGGACATAATGA[A/T]ATAAATAAATAAACA | 9873 |
rs562067844 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097166 | CACCACCAGGCCTGG[C/G]TGATTTTTGTATTTT | 9873 |
rs562070132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881948 | AGATTGAGACCATCC[A/T]GACTAACACGGTGAA | 9873 |
rs562091358 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136565 | TAATAATAATAAAAA[A/G]AATTATCTACTACTA | 9873 |
rs562102142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041887 | AGTAGTTTTATAGTT[C/T]TGGGTCCTAGGTTTA | 9873 |
rs562104398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122413 | CCAGGAAAGCAGGTA[C/T]ACAGGCATCCCCTCA | 9873 |
rs562105186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011659 | GCCATCACACAATCT[C/T]CTGGCAGCTCCCTAT | 9873 |
rs562116565 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109066 | TGGATTTGCTTTTGG[A/G]TTCTCTATTCTGTTC | 9873 |
rs562132699 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089431 | CAATTCTATTCCTAG[C/G]TGTATATCCATGAAA | 9873 |
rs562137374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006446 | ATTGATTCCTCATTT[A/G]TCTATCATATCTGCT | 9873 |
rs562154037 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106766 | TGCTTAAAGTATTCA[C/G]TACAGTAACATGCTG | 9873 |
rs562166562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121360 | ATTATTCCCACTCTA[C/T]ACAGATGAAGGACAC | 9873 |
rs562167760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003261 | TCAACTGGCAAATGG[A/C]GAAATAACAAAAATA | 9873 |
rs562184062 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905175 | TTTAATTTCTTCTGA[C/T]GGTAATTATTGTCGG | 9873 |
rs562197387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941452 | TTGGATGTCAGTTTG[C/T]TTAGTATAAAATATA | 9873 |
rs562197947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926837 | GTTGATAGTTTTGAA[A/T]TTAGATGTAGAAGCA | 9873 |
rs562198853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853004 | GAAGGCAGAAGGTGG[A/G]AGGAGGGAGAGGATT | 9873 |
rs562198855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998686 | TAAGAAGCTAATAGT[A/G]GAGGAAAAAATTGAT | 9873 |
rs562199319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007399 | GCTGAGGCAGAAGGA[C/T]TGCTTGAGGCCAGGA | 9873 |
rs562208746 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095340 | TAAGTGACAATATCA[C/T]ATTCCACAGCTTATA | 9873 |
rs562221153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896981 | ACAGGTGCCCGCCAC[C/T]ACGCCCGGCTAATTT | 9873 |
rs562229425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841979 | CTGACTTCCCCAGGT[A/T]TTGTGCATGTTAGGC | 9873 |
rs562237297 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865376 | TATTATTAGATCTTC[A/C]ACAAAATGTAATCTC | 9873 |
rs562241608 | in-del | -/TCTGTTCAGACCA | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143511 | CATGAACCTTCCTGC[-/TCTGTTCAGACCA]TCTACGGGGGAGTTT | 9873 |
rs562242563 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886109 | GGTGTTAGAAAACCA[C/T]TAGTTTAGTTTAAAC | 9873 |
rs562255277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891005 | TCACTGCAGCCTCAA[C/T]CTCCGGGCTCAAGTG | 9873 |
rs562257730 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007275 | TTTATGAATATCATA[C/T]AAGATATCTAGGAAA | 9873 |
rs562259109 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032447 | CCAAGGTTGGTCTCA[A/C]ACTCCTGGCCTTAAG | 9873 |
rs562259604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999244 | TGCTTAGATGTAACA[C/T]AGATCATCAGCAATA | 9873 |
rs562269939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873898 | ATCAAAAACTGCCAA[C/T]TACCTTCTAACTAGA | 9873 |
rs562271861 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889327 | TTCAACATATGTCTC[C/T]TCCCCTGCCCATAAT | 9873 |
rs562286444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917384 | GCACCTTTGTTGCAA[A/G]TCAATTGACCATAGA | 9873 |
rs562294337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112893 | CTCGTCTTGAACTCC[A/T]GACCTCAAATAATCC | 9873 |
rs562309312 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962763 | CAGGTTAAAATAAAA[A/T]AAAAAATCACACCAA | 9873 |
rs562332145 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120369 | AAGTCTATTAAGTAT[A/T]AATTGGCCAACAATG | 9873 |
rs562346779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107258 | CAGGGTTTCACCATG[C/T]TGGCCAGGATAGTCG | 9873 |
rs562354880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959293 | GGAGTGCAGTGGCCC[A/G]ATCTCGGCTCACTGC | 9873 |
rs562356630 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997787 | CTTCCTGCAATCTCT[A/G]CCTCCTGTGCTCAAG | 9873 |
rs562360473 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090454 | ATGGTCTCGATCTGC[C/T]GACCTCGTGATCCGC | 9873 |
rs562377488 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120900 | GCACTGGATGTTATG[A/G]GAACACACAGGCAGA | 9873 |
rs562389466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971531 | ACATGAACAGGACTG[A/G]ACACACTACTGCTGG | 9873 |
rs562393211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035206 | TATGTATGTATGTAC[A/G]TACTAAGACAAGGTC | 9873 |
rs562397118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128937 | AGTGTAGTGGTGTGA[C/T]CTCAGCTCACTGCAA | 9873 |
rs562414145 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908136 | GAACATGTGAAATTT[A/G]TCTTTCTGTGCCTAG | 9873 |
rs562438789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951784 | TTGATTTGAGGTTTA[C/T]CCTTTCACAATCTCT | 9873 |
rs562442277 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021466 | GCAAGAACAGAAAAC[G/T]AAATAATATATGTTC | 9873 |
rs562455093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900625 | CCAGGCTTCAAAGAA[G/T]TCAAATCACAGGAGA | 9873 |
rs562461078 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845543 | CAATGTAAGCAGACA[C/T]TAGCTTGATCATCCC | 9873 |
rs562466244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885457 | AACTAACAAACACAG[C/T]CTAGTTTGGCATACT | 9873 |
rs562492150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129078 | AGATTTCACCATGTT[A/T]GCCAGGATGGTCTCG | 9873 |
rs562502229 | in-del | -/AAGG | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883058 | GTAATGGGAAAAGCA[-/AAGG]TACTCTTTAAAATAT | 9873 |
rs562509853 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998086 | TACACAGAGAAAAAA[C/G]GGTGGAAAACAAAAT | 9873 |
rs562511782 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037373 | TAGTGACATATCCAT[C/T]ATTACAGTATCATAG | 9873 |
rs562513301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951145 | ACTCCAAACCATTGC[A/G]TTAGAAATAATTAAC | 9873 |
rs562519702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898564 | GAGTATATAGTTCTC[C/T]ATTTACCATCATATA | 9873 |
rs562532450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101167 | CTGAGGTTTAGTTCC[C/G]ACCTGAAGGAGAAAC | 9873 |
rs562557852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844793 | AACAAAAATAAGGCA[A/G]AAAAGGGGTCATTTT | 9873 |
rs562558807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052627 | AAACAAATTCTTAGT[G/T]TTTCTGCAAGATAAA | 9873 |
rs562569534 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838109 | TGGCTACTAGTTCAG[C/G]CCCTCCATATTAGCT | 9873 |
rs562577359 | in-del | -/GTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041595 | TTATGGAGTTTTTTT[-/GTT]TGTTTGTTTGCTACT | 9873 |
rs562578024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900160 | CCTCTTATACATGTA[C/T]ATACATAACTTTCAT | 9873 |
rs562588493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129763 | CATGGGAAAACTGTC[C/T]TCCAGGAAACTGGTC | 9873 |
rs562601174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914617 | TCTTCAACAAACCTG[A/T]CAAAAAGCAATGGGG | 9873 |
rs562604126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944519 | CTCTCTCACCACTCC[C/T]ATTCAACATAGTGTT | 9873 |
rs562608719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025008 | AGAAGTTGGCAAGGT[C/T]GTGGAGAAAAAGAAC | 9873 |
rs562627602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038543 | GAAATCTTGTCCTTT[C/G]TAGCAACATGAATGT | 9873 |
rs562629065 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100138 | CATGTGCTGCCCCCA[A/C]CACTCTTCTCACTCC | 9873 |
rs562631823 | in-del | -/AT | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077170 | TCGTTCTACTTTCAC[-/AT]ATGTTTGAAAACTTT | 9873 |
rs562642395 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011994 | AACATTTTAAATATA[C/T]AAACCCTTTGATCCA | 9873 |
rs562651284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137198 | TCAATATTGTCTTTG[A/G]AAAAAAAAAGCAAAT | 9873 |
rs562661192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093163 | TACTGTCACACATCA[C/T]TGCAGAAGAAGTGAA | 9873 |
rs562662362 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984707 | GAAAAACTCACTCAC[A/C]TCTGGCCCAGAATAT | 9873 |
rs562670921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930645 | AATTATTTGGGAGCC[C/T]GAGGCATAAGAATTG | 9873 |
rs562680219 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855689 | TTACCCATCATAGCT[A/G]AAAGGCATTTATTAA | 9873 |
rs562691192 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924324 | GCTCTATTGCCCAGG[C/T]TGGAGTGCAGTGGCA | 9873 |
rs562726992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037858 | GTGGACAACTTTAGG[A/C]AAAGAAGAAGGCAGT | 9873 |
rs562728689 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937979 | TCTGAATGGTAAGGG[A/C]AACAACAGAATAATG | 9873 |
rs562757336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930031 | AGAATGAGGCATTTA[C/T]CTTAATTGGGTCACC | 9873 |
rs562759773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922804 | ATTCACCCAATATAA[A/G]TCACCATTTTAATAA | 9873 |
rs562772118 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069466 | ATACATATATACACA[C/T]ATCTCTAAAAAGAAC | 9873 |
rs562793401 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041839 | TTTTTGCCTAGGCCA[A/G]TGTCCTGGAGTATTT | 9873 |
rs562819792 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137939 | CAGAAGGCCACAGAG[A/G]AGTGATCTATAATAA | 9873 |
rs562837216 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945951 | ACACTGTTGGTGGGA[A/C]TGTAAACTAGTTCAA | 9873 |
rs562842709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070031 | TGAATTTCCAGGTGG[C/T]GAAAGTAAAAAGGGA | 9873 |
rs562856542 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841666 | ACTGCTCTGTACTCA[C/T]GCCTTTTCTCTAAAG | 9873 |
rs562871397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017014 | TTGAGACAAGGCCTC[A/G]TTCCAATGCCCAGGC | 9873 |
rs562873366 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895176 | TGCCTGGCCTCTCAG[C/G]AGAGCACACTGGAGA | 9873 |
rs562875002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946415 | GTGGGGGAGGGGGGA[A/G]GGATAGCATTTGGAG | 9873 |
rs562876635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077152 | AAAGTTTGTTACGCT[A/C]ATTCGTTCTACTTTC | 9873 |
rs562904275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113662 | TCGTCATAGTCTGGG[A/C]TTGTTTGTACCCGTC | 9873 |
rs562908353 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73078008 | CTGGGATGCTGTTAA[C/T]GTGTTTCTTTACCTG | 9873 |
rs562936980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862028 | ATCATCAATGCAATT[A/G]CACCATATTAGCAGA | 9873 |
rs562937285 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973999 | AGGAGCAATTAATTG[C/T]GAAATAATCAAATAT | 9873 |
rs562940411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068736 | ACACTTTGGGAGGCC[A/G]AGGCAAGAGGACTGC | 9873 |
rs562948220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953381 | TTCTGCTTTCTGAAA[C/T]ATCTACATTTGGAAA | 9873 |
rs562957319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969018 | TGATATACACACATA[A/T]ATACATATGCTACTA | 9873 |
rs562965943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926604 | GAACACTCCAAGGGA[C/T]GATATGCCTACAGAG | 9873 |
rs562967617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112809 | ATACACTATCATGCC[C/T]GGCTAACATTTATTT | 9873 |
rs562987496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960147 | CTGGTGAGGCTTCTG[A/G]AAGCTTACAGTCATA | 9873 |
rs562995711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847432 | CGTGCTGGGCATTGT[C/T]CTAGGGGCTGAAGAC | 9873 |
rs563026577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126895 | ATAAAAAAATTTGCC[A/G]AGCATCGTGTTGCAC | 9873 |
rs563031596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119710 | CCTTGGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 9873 |
rs563050440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894575 | TATGAAGTATATTAA[C/T]ATATGGTTAATTATT | 9873 |
rs563052633 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839688 | GGGAGAAGGAACATG[C/T]CTGGAAGGGAACATA | 9873 |
rs563068159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952627 | ACCATGCCTGGCCTA[C/T]AGTTAATTTTGGTAA | 9873 |
rs563074975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109531 | TTCACTGTTGGCATA[C/T]AGAAATCTTACTGAT | 9873 |
rs563078798 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952275 | CTAGTATTTTTAGAG[A/C]AAAAACAATTCCATA | 9873 |
rs563082282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901663 | TTAAAAATGGTAATT[C/T]TTGTGTTATGTGTAT | 9873 |
rs563086769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134598 | GAGGTCTCTAGACCA[C/T]CAGGTGTCTGCAAAG | 9873 |
rs563089138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918054 | ATTATATGCATTTAT[C/T]TATATCTTTTATTTC | 9873 |
rs563098953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119289 | GCCTGCACAACAGAG[C/T]GAGACTCTGCCTCAA | 9873 |
rs563114888 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081603 | ACTATCTGAGCTCAC[A/T]GCAATCTCCGGCTCC | 9873 |
rs563132107 | snp | A/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73000997 | AACAATACCCTTTTT[A/T]GTTGCTGTTCTTTTA | 9873 |
rs563136950 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966926 | GAAAGTGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 9873 |
rs563140222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110201 | AGGGTACTGCTGGCC[C/T]CACAGAATGAGTTTA | 9873 |
rs563142324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010368 | CTTCTTTAATATCAA[A/C]ATTTTGAATTCTTTT | 9873 |
rs563159377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102303 | ATATAGATAGACTCT[A/G]GGGAAATTTTTGGCA | 9873 |
rs563168518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058083 | ACAGGGTTTCACCGT[C/G]TTAGCCAGGATGGTC | 9873 |
rs563176081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072365 | GAGTACTAACATTTA[A/G]TTATAGCCACCATTT | 9873 |
rs563183798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135389 | TCCACCTGACTAAAA[C/T]TCAATAATTTTTCCA | 9873 |
rs563193470 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993936 | TAAATAAATATCGGA[A/T]AGAAAAGCCAGGCTT | 9873 |
rs563193561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001978 | TATTTATAAACACAA[C/T]CGATAATTTATAACA | 9873 |
rs563205721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019878 | GCCTAATTAATTTGC[C/T]AAGGAAAATAAACCT | 9873 |
rs563241373 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058779 | TACCATGTTGGCCAG[G/T]CTGGTCTTGAACTTC | 9873 |
rs563246812 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989761 | ACACTGCCTCAGGAC[C/T]TTTCTGAGTATCCAA | 9873 |
rs563249980 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070313 | CACTCTGTTTTACTG[A/G]TAACATTCCAGCACT | 9873 |
rs563284749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910793 | CTGCCACATCCCCCT[C/G]TCCGAGAAACACCCA | 9873 |
rs563309694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942327 | GAAGCAGATGCCAGC[A/G]GCATGCTCCCTGTAC | 9873 |
rs563310095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955855 | GAGACCAAACATGTA[C/T]TTCAAATTATAATAT | 9873 |
rs563320275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905312 | ATATAGTAGGTATTT[A/G]TATTTATGGGGTACA | 9873 |
rs563320999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971416 | TTGTGATTATGCTAC[A/G]TTAAATGGCAAAAGG | 9873 |
rs563321299 | in-del | -/CGCTCCCGGTCGGCCGCCTGCGCCGC | 0.0244538 | 0.107838 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142235 | CAGCCGCGTTGTCCG[-/CGCTCCCGGTCGGCCGCCTGCGCCGC]CGCTCCCGGCGGACG | 9873 |
rs563330558 | in-del | -/TGATGCTAGAACAAT | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022964 | GTCTCAATCAACAAG[-/TGATGCTAGAACAAT]TGAATGACCATAAAC | 9873 |
rs563336705 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852375 | CCCATTACTGGACAC[A/G]TACCCAAAGGTACAT | 9873 |
rs563348156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943107 | AGTGATTCTCCTTCC[C/T]TGGCCTCCTGAGTAG | 9873 |
rs563352250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138730 | TCTCTGCCTCAGCCT[C/T]CTGAGTAGCTAGGAC | 9873 |
rs563361656 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027644 | AAAAAGAAGCCAAAT[A/G]TTAATAGCCAAAACA | 9873 |
rs563397957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091558 | CATCTCAAAAAAAAG[A/G]AAAAAGAAAAGAAAG | 9873 |
rs563423343 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049698 | ATAAAAAAAAAAAAA[A/G]AAAGAAAAAGGGGGA | 9873 |
rs563428955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020508 | ACAATGAACAAGTTC[A/G]CTGCATAAGCTGGAT | 9873 |
rs563434210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116979 | TATTGTTATATCTCT[A/G]TTTCATTTTTAGCAT | 9873 |
rs563452718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857365 | GTCACTTGACAGAAC[C/T]TCAATCAAAACTATT | 9873 |
rs563454394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866229 | ATAGTAGGAGATATT[C/T]CATGAGATGGAGCAA | 9873 |
rs563461015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092086 | TCTGAGAAGCCTTCC[C/T]GAATTCCTCTTGTGA | 9873 |
rs563464328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098240 | ACAGCGTAAGTTTTG[A/G]TATTGTATATTTTTG | 9873 |
rs563470065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964883 | CAAGTTCTGCCTCCC[A/G]GGTTCACGCCATTCT | 9873 |
rs563490563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013017 | CTTCCTCACACCCCT[A/C]GAATCCACCTTTACA | 9873 |
rs563498037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116427 | TGGGTGTTTTTCTCA[C/T]TCTGTGAAACATTCC | 9873 |
rs563502477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973547 | TATCACAGGGCATGA[C/T]ACTATCTAAGACAAC | 9873 |
rs563506449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956527 | ACTTATAATCAACAG[A/C]ATTAATTTCTCTTAC | 9873 |
rs563509998 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FCHSD2 | GRCh38.p7 | 11:73141051 | TCATCCACCCAGTGC[A/C]CAGAGTAGACATTCA | 9873 |
rs563526271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004474 | CTAACAGTTACTCAG[G/T]CCTATAAGAACCCAC | 9873 |
rs563527274 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898755 | TTTTTTTAAAGACAG[C/G]GTCTTGCTCTGTCAC | 9873 |
rs563529432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989499 | TATGTTTGGGTAACC[A/G]ACAGTGCAAAGGGTA | 9873 |
rs563544130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867624 | TTGGTAGATAGGCAT[C/T]GATAACCCAAATAGT | 9873 |
rs563553208 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986635 | TATTCCCAGTTCTCC[-/T]TTTTTTTACAGTCAT | 9873 |
rs563566111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843858 | AAATAAATAAATAAA[A/G]TTAGTCAGGCATGGT | 9873 |
rs563570925 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131528 | GTGAGACTTCGTCTC[-/A]AAAAAAAATAAAAAT | 9873 |
rs563585834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123596 | TATGTTTAATTCTGG[A/G]AATTCAAAATATTTC | 9873 |
rs563589682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997383 | TAGCATTCTATCCAC[C/T]TGCCAGAAGAAAGCT | 9873 |
rs563591349 | in-del | -/AATA | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055671 | TCACTTAAATTTTTT[-/AATA]GATAAAACATACCAT | 9873 |
rs563605341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859011 | TTTTAGGTTATGACA[C/T]AGGGAGAAGAAACCC | 9873 |
rs563621415 | snp | A/C/G | 0.000462897 | 0.0152069 | missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843170 | GGCATCTCCGTTGAG[A/C/G]CTGCCTGAAACGAGT | 9873 |
rs563624490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966252 | GCAACCTCTGCCTCC[C/T]GGGTTCATGCAATTC | 9873 |
rs563638326 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115512 | TCCAACTCTATACTT[A/T]CGTGTCGTTTTCATG | 9873 |
rs563661765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051082 | ACATTTTGGGAGGCC[A/G]AGGTGGGAGGATCGC | 9873 |
rs563670251 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880123 | AACAAAAAACCCCAA[C/T]CCCAGGAATAAATTT | 9873 |
rs563705177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890027 | GATGGATCAGAAGGC[C/G]TTCACTTAATCAGCA | 9873 |
rs563732024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102223 | AGAAAATTAACAATT[C/G]CAAGTGCTGATAAGG | 9873 |
rs563733061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021771 | AGATGCAGAAGAATA[A/C]GTCCTTAACCTAATA | 9873 |
rs563733835 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911246 | TTATTGAAGAGATTG[C/T]CCTTTCTCCAATGTA | 9873 |
rs563744279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945802 | ATGAAAAAATGCTCA[C/T]CATCAATGGACATCA | 9873 |
rs563748006 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035985 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAAGCGT | 9873 |
rs563775873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876238 | GGGAGGCTGAGGTGG[C/G]AGGATTGCTTGAGGC | 9873 |
rs563793101 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083650 | CTGTCCTTAAGCCAC[A/G]GAAAAGAAGTATACC | 9873 |
rs563796409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868116 | ATGCCCATCAATGAT[C/T]GACTGGATAAAGAAA | 9873 |
rs563813641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028937 | AAGCCACGTGAAACT[A/G]TGAGTCCATGAAACC | 9873 |
rs563819935 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093762 | ATGCACCACCATGCC[A/G]AGCTAATTTTTTTTG | 9873 |
rs563837415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928085 | GTCTTTCTTGCCTTG[A/C]TTTAAAATCATCAAT | 9873 |
rs563837940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839485 | AATCCTCTGAATGAG[A/C]GTTGACAATAGCCCA | 9873 |
rs563862635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986159 | AAAAATTGGGTTTAA[A/G]AGATTCCTGTTATTT | 9873 |
rs563862794 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846169 | GATGAGTAAGCTGCT[C/G]CTCCTTTTGCTCTTT | 9873 |
rs563863558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875482 | GGGACCAGAAGCATA[C/T]GCCACCACATCTAAT | 9873 |
rs563874327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029461 | GCTCTTAGCTCAGCT[A/G]TGGCTACCCATCTTT | 9873 |
rs563899349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977667 | AATCACTAAAAAGTC[A/G]GGAAACAACAGGTGC | 9873 |
rs563900933 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024518 | AAAAGCTCAGTGTTG[C/G]AGTGGGACTTAGAAA | 9873 |
rs563901925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000894 | AGAAACATATGGGAC[C/T]ATATAGTTTTAAATA | 9873 |
rs563924067 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087648 | AGGCAGAGGTTGCAG[C/T]GGGCCGAGATCACAC | 9873 |
rs563926430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986505 | TGAGCCACCGTGCCC[A/G]GCCCCAATTATTTTA | 9873 |
rs563929243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920527 | GGTGGACCACTTGAG[A/G]CCAGGACTTCAAGAC | 9873 |
rs563937033 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057822 | GTTCCCCTCAGTTCT[C/T]GAGGGATCTAAGAGG | 9873 |
rs563941863 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045774 | GGACTGTTGTGGGGT[C/G]GGGGGAGCGGGGAGG | 9873 |
rs563945308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075227 | AAATTGCAATAATCA[C/T]CTGAGAAAACCATTT | 9873 |
rs563965617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978621 | ACTGGATTATAGGAG[C/T]GATTTCCCTGATGCT | 9873 |
rs563968857 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919561 | CATATAAAATGAACA[C/T]GGTAATGGCGACCTC | 9873 |
rs563983811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870769 | GCTGGGCGTGGTGGC[A/G]GGTGCCTGTAGTCCC | 9873 |
rs564008667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862937 | ATATATGATTAATTT[G/T]TTTTTTAAAGAGACT | 9873 |
rs564012068 | snp | A/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067017 | ATAAATCATTCTACT[A/G]TAAAGACACATGCAC | 9873 |
rs564020678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871738 | CACTCCAGTGACAAA[C/T]ACCTTTGGTACATAA | 9873 |
rs564054547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931689 | AGAATTGCTTGGACC[C/T]GGGAGGTGGAGGTTG | 9873 |
rs564061360 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045159 | GCAGCCAAAAAACAC[A/G]TGAAAAAATGCTCAT | 9873 |
rs564068271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893357 | TTCTCACTCTATTGC[C/T]CAGGCTGGAGTGCGG | 9873 |
rs564068384 | snp | A/C | 0.000155328 | 0.00881134 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902511 | AAACACAACTGAACA[A/C]CACATGAAATGAAAA | 9873 |
rs564102953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116923 | AGAGTAATTATATTT[C/T]TTCATGTAAAACCTT | 9873 |
rs564113323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963921 | ACAACTCTGTGTCAT[A/G]AATAGATTTCACAGT | 9873 |
rs564171013 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997400 | GCCAGAAGAAAGCTT[A/C]ACCCTCTTTGGAAAT | 9873 |
rs564177692 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893465 | AGACCACAGCATATG[A/C/T]CATCACACGCAGATA | 9873 |
rs564193619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025856 | ACCAACTCAGTAACA[C/T]CCTTCTGGTCTCCCG | 9873 |
rs564203322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116362 | TTTGATTGCTTGTAC[A/T]GTCCTGTTAGATTGT | 9873 |
rs564207897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138660 | GTTGCCCAGGCTGGA[A/G]AGCAGTGGTGCCATC | 9873 |
rs564208734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032496 | ATCCCAAGGTGCTAG[C/G]ATTACAGGTGTGAGC | 9873 |
rs564211100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040173 | GGTGGCCAGTCTGCA[C/G]CTCTGTGTCAGCAGC | 9873 |
rs564224963 | snp | A/C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069843 | AATAAAACATCTAGA[A/C/T]TCATAAATGATACAT | 9873 |
rs564236016 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003733 | CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 9873 |
rs564237149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969599 | GAATACAAGAAGCAT[C/T]GAAGATATAAAAAAC | 9873 |
rs564239887 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127967 | CCAGGCGTTGTGAGA[G/T]CACACCACTGTACTC | 9873 |
rs564249103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017785 | GCTAAATTCTCACCC[C/G]TCCCTTTTAATCTGA | 9873 |
rs564274824 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025506 | GGGTGGAGGGTGGGA[A/G]GAGGGAGATAATGAG | 9873 |
rs564277024 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124027 | AATGTCCATCAATGA[C/T]AGACTGGATTAAGAA | 9873 |
rs564278477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033017 | AGATTGGCCGGGTGC[A/G]GTGGCTCACACCTGT | 9873 |
rs564294699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923917 | GAAATACAGCTCTGC[A/G]TGACAGAGCAAGACT | 9873 |
rs564294829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131244 | AAAATTAGGCCGGGC[A/G]CAGTGGTTCACGCCT | 9873 |
rs564308740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909723 | GCGCCTCTGCCTGGC[C/T]GCCACCCCGTCTGGT | 9873 |
rs564311992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025199 | CACACATATGTTCAC[G/T]GCAACACTATTCACA | 9873 |
rs564333289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924393 | TGCCATTCTCCTGCC[A/G]CAGCCTCCCGAGTAG | 9873 |
rs564334274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896310 | GGGAAACCTGAGGAA[A/G]TTTCCGTGTTTTTCC | 9873 |
rs564348751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879475 | ATGACAGAGATGATG[C/G]AATGAGTAGACAAGA | 9873 |
rs564354199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130420 | CTATTCTTAACCCTA[A/G]AGATAAGTAACTTTC | 9873 |
rs564354708 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041065 | TGACAGAATTTCATT[C/G]TTTTTTATGGCTAAA | 9873 |
rs564368847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855682 | AGGTATATTACCCAT[C/G]ATAGCTAAAAGGCAT | 9873 |
rs564369591 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898600 | CTCAAAAATAACACC[A/T]GGTTGCATCCCACTT | 9873 |
rs564370520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888203 | GAAAAAATCTAGGTA[C/T]GGCCAGAAAGGCAGA | 9873 |
rs564388282 | in-del | -/TCAAGA | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032781 | GGGAACATAGCCCCT[-/TCAAGA]AACTTCATACAAGCT | 9873 |
rs564391399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111011 | ATTGATTTCTAGTTT[C/T]ATTCCATTGTGATCA | 9873 |
rs564393493 | snp | C/T | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144431 | GAGGCAGGAGAATAG[C/T]GTGAACCCGGGAGGT | 9873 |
rs564398752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903470 | GTGATCCACCGGCCT[C/T]GGCCTCCTAAAGTGC | 9873 |
rs564405351 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922855 | TGGCTTTTAGTACAC[C/T]GACAAAGTTGTTTAA | 9873 |
rs564420075 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916025 | AAATTATGAGAACAC[A/G]TGGGAACAACGCACA | 9873 |
rs564422477 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890050 | AATCAGCACTCAAAA[C/G]ATGAGGCACGCTCCA | 9873 |
rs564431834 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121176 | ATACACATACACATA[C/T]ACACACACACACACA | 9873 |
rs564463191 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848981 | GAAGTATTATGAATT[C/T]AAATATAAAATGAAA | 9873 |
rs564473242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925537 | TCTTTAAAACAAACA[A/G]ACAAACAAATAAATT | 9873 |
rs564479053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034712 | AACTTCAATAAACTT[A/G]TTTGCACAAAATGAC | 9873 |
rs564494233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018827 | AAATTTGACCATCTT[A/C]ACTATTTTAAGAGAA | 9873 |
rs564498808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995092 | ATATGTGGCCTTATG[A/T]TTCTCACTTCTTTCA | 9873 |
rs564503709 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982280 | ACTTTCAAGGAAAGA[A/C]CTTGCAGTTTCTGGC | 9873 |
rs564510184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110354 | GATATTTTATTACGG[C/T]TTCAATCCTGTTATT | 9873 |
rs564513640 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861919 | CTGGGCAACAAAAGC[A/G]AAACGCCGTCTCAAA | 9873 |
rs564528720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014061 | AGAATTTCATCTCTC[C/T]TCTCTTCCTCCTTAG | 9873 |
rs564540235 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055378 | ATAAAGAAACACTGA[A/C]GTAAATACTAATAAT | 9873 |
rs564546925 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142059 | GACCCCAGCCAGAGA[A/G]CGAGTGTGAGGAGAC | 9873 |
rs564551523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946797 | CATTTTCATTTTACA[A/G]AGCAGGAAACTGAGT | 9873 |
rs564551627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954909 | ATATATACAGAAACA[C/G]ATCTGGCTGTATGTA | 9873 |
rs564560959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987730 | CCTGTGGGCTGTGGC[C/T]AAATTATTTGTTTAT | 9873 |
rs564565518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020699 | TATTATTTTAAATTA[C/T]ATAATAAATTGTCTT | 9873 |
rs564578813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910017 | TCTAGGAAGTGAGGA[A/G]CGCCTCTGCCCGGCC | 9873 |
rs564586411 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880426 | ACCAATGGAACAGAA[C/G]AGACATCCCAGAAAT | 9873 |
rs564615732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904030 | ATCTGGGAACTGGGC[G/T]AACCAAACAGACTAC | 9873 |
rs564617030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933302 | AAGTTATTCTTCCTA[C/T]CAAGCAGATAGTGCC | 9873 |
rs564619126 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113836 | GCTATGTTTCTTGAA[A/C]ACTTGTAGTGGTACT | 9873 |
rs564633049 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131850 | CTTATTAAAAGAGTT[A/C]TTTTAAACTTATTTA | 9873 |
rs564634419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994155 | GACCGAGACATACAA[C/T]AGTGGGAGAATTATT | 9873 |
rs564644417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880440 | ACAGACATCCCAGAA[A/G]TAATGTACTTATAGC | 9873 |
rs564670288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840293 | ATGAAGCCAAAAGAA[A/G]CCAGTGGTAAAGGAA | 9873 |
rs564694943 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099270 | AGGATGGCTGTAAAA[C/T]AACACAAAACAAAAC | 9873 |
rs564696286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104809 | CTGACCTCAGTGATC[C/T]GGCCTCCCAAAGTGC | 9873 |
rs564713464 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954323 | ATGCAATTCTCTCAA[C/T]TCAGCCTCCTGAGTA | 9873 |
rs564723888 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097079 | ACAATCTCAGCTCAC[G/T]GCAGCCTCGACCTCC | 9873 |
rs564723974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088587 | GTTTTAGTAAACATA[C/T]AATGTTTGAAAAAAA | 9873 |
rs564727193 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031891 | CACTGTATTAGATGC[C/T]GGGGGAATAGCAATA | 9873 |
rs564737496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022450 | ATATTCCAAAGTTAA[C/T]TGCTCTCCTACATAC | 9873 |
rs564753573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044133 | ACTGATACATCCAAG[A/G]CCTGCTACTATATGT | 9873 |
rs564760860 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941286 | TAAATATTTGTTAAA[A/T]TATGAATTAATGAAT | 9873 |
rs564764106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059030 | CCATTTTAGTTTTTA[A/T]GCTAAGCTAAGAAAT | 9873 |
rs564772243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966183 | TTTTTTTTTTTTCAG[C/T]TGGTCTCACTCTGTC | 9873 |
rs564787214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089322 | GAAATCAGAACTCTC[A/G]TAGCGTTAGTGGAAA | 9873 |
rs564791775 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061087 | GCAGAAGGCAGATGA[C/T]TTCTGCATGTCCAAC | 9873 |
rs564795664 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851599 | AAACAAAAAATTAGC[C/T]GGGCATGGTGGCATG | 9873 |
rs564816913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037010 | TAGGGACTGCCAAAT[A/G]CTGATATCAATTCAA | 9873 |
rs564824825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988301 | TTATCTTTCCTCAAA[C/T]TGTCACTGCAAAAAT | 9873 |
rs564832304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907274 | TACAATCATGTCATC[G/T]GCAAAAAGACACAAT | 9873 |
rs564848859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965533 | GTACATACTGCCATT[A/G]TAGTATTTTTTTAAA | 9873 |
rs564851276 | in-del | -/TTTTT | 0.00875682 | 0.0655876 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110151 | TCTGTAGTTTTCTTC[-/TTTTT]TTTTTTGATGTGTCT | 9873 |
rs564866255 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023314 | AAAGGAAGTCCAAAT[A/C]TATAAAGAATTCCTA | 9873 |
rs564879535 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879134 | ACAAAACAAAAAAAC[-/A]AAAAAAAAAGATATT | 9873 |
rs564883005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912770 | GGCTTTTCCTTGCTG[A/G]GAGACTTTCTATTAC | 9873 |
rs564894734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125621 | GAGGCAAGAGGACTG[A/T]TTGAGCTCAAGGGGT | 9873 |
rs564905930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066925 | TGGAAGACAGTGTAG[C/T]GATTCCTCAAGGATC | 9873 |
rs564923052 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054066 | ATTCTAGCCTGCTGT[C/G]TGTTTCACTAAATAA | 9873 |
rs564926936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108026 | GTACTAATTTACATT[C/T]CCACCAACACTGTCT | 9873 |
rs564930348 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933973 | AATTAGCCAGGTGTG[A/G]TGGTATGTGGCTGTA | 9873 |
rs564930448 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000129 | ATCATCTTTGGCAAA[C/T]GGAAAATTGGGGGGT | 9873 |
rs564950089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958363 | TCTCTATCAAAAACA[G/T]AAAAATTAGCTGGGC | 9873 |
rs564953874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052553 | AATTGTACACTACTG[G/T]TACTACATACTGAAG | 9873 |
rs564960284 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124844 | CCCCAAACAAGATAA[A/T]TACAGACACTATACT | 9873 |
rs564965258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906483 | GCTTTCGGTGTTTTA[C/G]TCATGAAGTCTTTGC | 9873 |
rs564987727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059866 | ACAATCCTTGACTAA[C/T]AGAAGACTTGATAAA | 9873 |
rs564994910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999143 | ACATTCCCTTCTTGG[C/T]TTAAAGCAGTTTGAA | 9873 |
rs565023485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944444 | TCACAGCCAATATCA[C/T]ACTGAATGGGCAAAA | 9873 |
rs565023936 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917697 | TCAAGACTAGCCTGG[C/T]TAACATGACGAAACC | 9873 |
rs565048747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067868 | CTGCTGATAAAGACA[C/T]ACTCAAGACTGGGTA | 9873 |
rs565057112 | in-del | -/AAAAT | 0.0019996 | 0.0315563 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080965 | AAAAACAACAAAAAT[-/AAAAT]AAAATAAAATAAAAT | 9873 |
rs565057427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991554 | ATGCAAGGCTGGTTC[A/T]ACATACGCTGATCAA | 9873 |
rs565078733 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976453 | CGTGCTAATTTTTAA[A/G]TTTTTTTGTAGAGAC | 9873 |
rs565088259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998569 | TAATTTGGAACAAGG[A/C]TTGGGGAATAGTAAG | 9873 |
rs565089668 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884318 | CTAGATGTTAGGAAA[C/T]ACATGTTTATTCTTC | 9873 |
rs565095242 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040303 | ATTGTTTCGCAGTCA[A/T]GTGGAAAAACAAAAA | 9873 |
rs565111729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068603 | AGTTTTATCAGTTTT[C/T]ATACAGTTAACAAAA | 9873 |
rs565113329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844756 | ACAATCTCAAAATGT[A/G]AAATTAACTCCAAGT | 9873 |
rs565117899 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063368 | ATCAACACTATGAAG[-/A]AACTGCATCAACTAA | 9873 |
rs565132893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100032 | CGCTGCCTTCCCTGA[C/T]GCACCCCGGAAGGCG | 9873 |
rs565134858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092271 | TAGCTGGGACTATAG[A/G]TGTACACCACCACAC | 9873 |
rs565148324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990979 | GCAAGACTAATAAAG[A/G]AGAAAAGAGAGAAGA | 9873 |
rs565171678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061454 | GGAATACCAGTGAGA[C/T]AGAACGATTCACTTC | 9873 |
rs565173024 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837265 | CCCCAAATCATGGAG[A/G]AGATTCATTAATGGG | 9873 |
rs565175823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936888 | ATATTAAAAATAGGC[G/T]ATTTAAAATCTTTGT | 9873 |
rs565185548 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838069 | CACAGCCTCCTTTCT[A/G]TTAGTCTATGTGATG | 9873 |
rs565192277 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056258 | GGCTTACGAGCCAAG[A/G]TAGGGGTCCTGTGCA | 9873 |
rs565202395 | snp | C/G | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883519 | GGGGGATATATGAAG[C/G]GCTAAAAACTTATAA | 9873 |
rs565217183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132995 | GAAGATATACAAATG[A/G]CCAATAAGCACATGA | 9873 |
rs565235587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062005 | CCTGACCCCTGTTCC[C/T]CCTGACTGGGAGACA | 9873 |
rs565240327 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876663 | TGCAGTGGAGTTCGA[C/T]GAATGCCAATTAGGT | 9873 |
rs565242262 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901216 | GGCAACATGGTGAGA[-/C]CCCCCCCATCTCTAT | 9873 |
rs565245370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076980 | CCAGGCATGGTGGCG[A/G]GCACCTGTAGTCCCA | 9873 |
rs565265243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085151 | ACGGAAGAAGTTTCA[C/T]CTTAAACCTAAAGAC | 9873 |
rs565268454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983738 | TTGAAACCATGACAT[A/G]AGTCTCATAAAATAG | 9873 |
rs565287095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030849 | CCTAAAGCCTACTCT[C/T]TCAGCAAAAAATCCT | 9873 |
rs565289889 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085519 | CTCCCTTAATTTTTC[C/T]CTTTTTCCCCTTTTG | 9873 |
rs565304144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975599 | TCCTTACACATTGTA[C/T]GCATGCATCAAAATA | 9873 |
rs565319093 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910019 | TAGGAAGTGAGGAGC[A/G]CCTCTGCCCGGCCAC | 9873 |
rs565320514 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978597 | GGGGGAGGGTCCCTG[C/T]GGGAGGTGACTGGAT | 9873 |
rs565324719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914547 | AACAGACACATAGAC[C/G]AATGAAACAGAATAG | 9873 |
rs565328033 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076230 | ATAAAGACTAATATG[G/T]TTATTAGGCAGCATT | 9873 |
rs565348220 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023510 | ACATGTATTAGAATG[C/T]TAAATCCAAAAAATT | 9873 |
rs565353750 | in-del | -/TTGAT | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911933 | AATGACATTACTTTC[-/TTGAT]TTATTTTTCAGAATG | 9873 |
rs565362249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961535 | TGCTATGATTACAGG[C/T]GTGAGCCACCATACC | 9873 |
rs565377850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960053 | AAAGGAATATGTAAG[C/G]CTGGGTAGTCTATAA | 9873 |
rs565382465 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946762 | ACTCTACTTTTTACA[A/T]CCACCTTTAAGGTAG | 9873 |
rs565383764 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973179 | TCAAGACCAGCCTGA[C/T]CAACATGGAGAAACC | 9873 |
rs565383827 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016075 | TGGGAGGCCAAGGTA[C/G]ACAGATCACTTGAGG | 9873 |
rs565386542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071169 | GCTGCTCTAACTAGC[C/T]AATACCTTCTGTCAT | 9873 |
rs565393826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976468 | ATTTTTTTGTAGAGA[C/T]AAAGTCTCACTATGC | 9873 |
rs565396381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854264 | AGCACAGACTTGAAC[A/C]GATATTTGTAAACAA | 9873 |
rs565404153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015701 | TCCGAAAACACAGCA[A/G]AGGAAAGAAGTAATT | 9873 |
rs565427402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132177 | ATTTCAGAAATGTAA[G/T]AATGTAAAACAATGT | 9873 |
rs565429550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959487 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 9873 |
rs565450938 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962400 | TATAACCTACATCAA[C/T]AAAAGCTCTTTGATT | 9873 |
rs565454670 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906120 | TTCCTTTTTAATGAT[C/T]GCCATTCTGTTGTGA | 9873 |
rs565456986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953712 | ACAAAGAAAAGAAAT[A/C]GAGAATGAAGAAAAG | 9873 |
rs565461897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869905 | ACTTTCATAACTCCT[C/G]ACTGTCTACTGAGTA | 9873 |
rs565488161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139624 | AACCCAGTGAGAGCA[C/T]ATAACCATCTGGGGT | 9873 |
rs565489340 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119271 | TCATGCCATTGCATT[C/T]CAGCCTGCACAACAG | 9873 |
rs565526567 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909096 | CTGTTGCCGATACTG[C/T]CGTGATCTCAGCTCG | 9873 |
rs565527812 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969329 | TGGCTTTAAGTTATT[G/T]ATATCAGGAATAAAA | 9873 |
rs565537448 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903918 | ACCAACCATTTATTG[A/T]GAGAGTTTACCAGGT | 9873 |
rs565541067 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108793 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 9873 |
rs565563165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915712 | AATCCCAGCTACTCG[A/G]GAGGCTGAGGCAGGA | 9873 |
rs565569863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053857 | AATTGTTTTCTTTTT[C/T]CCTATGTATGACCAT | 9873 |
rs565576568 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116055 | AAATATGATGACTGC[A/G]GATTTTTAAATAAAT | 9873 |
rs565585231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901590 | ACCAAGTTATGACAG[C/T]GCACAGCACTGGAAA | 9873 |
rs565585372 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073635 | ACGCTCAATCTTTTT[-/A]AGTCAATCAATCCTT | 9873 |
rs565609111 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096294 | GTCTGTAATCCCAGC[A/G]CTTAGGGAGGCCAAG | 9873 |
rs565609619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855273 | CAAGAGCAAAACTCC[A/G]TCTCAAAAACAAACA | 9873 |
rs565621229 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086774 | CAACTGTACACCAGC[A/C]AATTAGATAAATTAA | 9873 |
rs565632744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871058 | AAAGTTCCTATTCTC[C/T]AAATTCAAGAAAGGG | 9873 |
rs565636660 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013302 | TAGAATTTCTTTTAC[C/T]AAACTGTCTGCCTGG | 9873 |
rs565645939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062971 | CAAGAAGAGCAACCC[C/T]AAGACACATAATCGT | 9873 |
rs565657372 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911955 | ATTTTTCAGAATGCT[C/T]ACTGTTCACATATAG | 9873 |
rs565661698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841394 | TTTTTGCCCTTCAGG[C/T]GAATATGTAGGTTTC | 9873 |
rs565681788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017311 | TAGGAATATATGTGG[G/T]CCCCTAACACTATAA | 9873 |
rs565713250 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987976 | AGAAATATTAAATGT[A/G]TTTTCCTGTAACATC | 9873 |
rs565730132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916114 | ATAACTAATGGGTAC[C/T]AGGCTTAATACGTGG | 9873 |
rs565740221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863754 | GATCAACATTATCAG[A/G]GAAATGGAAATTAAA | 9873 |
rs565746256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009947 | GGATGTCTAAATCTC[G/T]TTAGACTTGGGAAGT | 9873 |
rs565746385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018355 | TGGGTCTTACTATTT[A/G]TGTCTTTTTCTAAAA | 9873 |
rs565748781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002373 | TGTGTTGCACCAGCA[A/G]AAACTGTCAGCATAA | 9873 |
rs565775561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946977 | CAGCCATCTATGCAA[C/T]AGCTCACCCAGCTAC | 9873 |
rs565780006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983016 | ATAAAAGAAAGGGGC[C/T]GGGCGCGGTGGCTCA | 9873 |
rs565794161 | snp | C/T | | | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72844198 | TTTGGGAAGCAAAGG[C/T]AAACGAGAAGGCACT | 9873 |
rs565799572 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988843 | ATATAACACATGTAG[C/G]TCAAATGAAACCACC | 9873 |
rs565808062 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961045 | GTAACACACATGTGA[G/T]GCTGCCTTAGCACTG | 9873 |
rs565809219 | in-del | -/GAG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904366 | TGTTTTGTTCCTCTT[-/GAG]GAGGAGATTTCAACC | 9873 |
rs565814250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940452 | CAATAAATAGTAAAT[A/C]AGCTATTTTCCTTTC | 9873 |
rs565828083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902980 | AGATAAGGAAACACA[C/T]TGGTCTTTGCCATCT | 9873 |
rs565853751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855901 | TCTATACTCTTTGAA[C/T]TATTAGAATATGCAC | 9873 |
rs565855051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873293 | GAGATCGCGCCACTG[A/C]ACTCCAGCCCAGGCA | 9873 |
rs565861632 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846438 | GCCCGCCTTGGCCCC[A/G]CAACGTGCTGGGATT | 9873 |
rs565865774 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121374 | ACACAGATGAAGGAC[A/G]CTTAAAAAGGAAAAA | 9873 |
rs565873855 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111222 | AGAGTGATGTTTCTT[C/T]GCTGATTTTCTGTTT | 9873 |
rs565877440 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130650 | GTATTACCAAAACCC[C/T]AATTCTTTCAATTTC | 9873 |
rs565889221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873955 | AGGATACTACCGTGC[C/T]ACTTTAACCAATCAA | 9873 |
rs565901673 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056683 | AGGTAGAGAAGAGAG[A/C]ATAACAGAACAATAA | 9873 |
rs565910593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047222 | ACCCATATTATTTGA[A/G]TTGTTAAAACTACCA | 9873 |
rs565926075 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880912 | AACAACAAACAAACA[A/C]CCACACTATAGAACT | 9873 |
rs565935959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088786 | AGTTCACACTTTCAC[C/T]ATTTAAAAACCTCTA | 9873 |
rs565936733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138301 | ACACAAACTCAGGAC[G/T]GTCTGACTGCAGTGT | 9873 |
rs565940864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865743 | TGAGATTCTGGAGTT[C/G]GTGGGGGTGGGGAGT | 9873 |
rs565941079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947955 | AATGGTATAATCTTA[C/T]ACAACATAATTTTTA | 9873 |
rs565945731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904318 | GATCACCTCTCTAGT[C/T]GCCAAACTTGTCCTC | 9873 |
rs565957471 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124382 | ACCTGCACATTGTGC[A/C]CATGTACCCTAGAAC | 9873 |
rs565958524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034248 | CTCCCTCCCCTTTAA[A/G]GTTTTTCTTTAAATA | 9873 |
rs565977644 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033050 | TCCCAGCACTTTGGG[A/G]GGCTGAGGCATGCGG | 9873 |
rs565997531 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870050 | TTGCTGTTCCTCTGA[C/T]CCATCATGTGCTTGC | 9873 |
rs565999722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137752 | CAGCATACACAGGGG[C/T]ATGAATGTAGAGTGC | 9873 |
rs566001330 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081113 | TATTTTACATTTTAA[A/G]TAATAAACATGTCCT | 9873 |
rs566001700 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093381 | GGGACCCACAAAATT[G/T]CAAGTCGTGTCAGAA | 9873 |
rs566029766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940944 | AAATCCTGACACCCA[A/G]TGGATCACCAAAGCA | 9873 |
rs566032492 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112464 | ATTAAATGCCTTAAG[A/G]TAGTCTTCTTTGGGC | 9873 |
rs566038300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083500 | GTTGCAGTGAGCCAA[G/T]ATTGCGCCACTGTAC | 9873 |
rs566042940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971060 | GATAAGTTATCCCTA[C/T]TGACCCCCCTGCCCA | 9873 |
rs566044513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932951 | TGATGTTACATAACA[C/T]TTATAAAATCGTATA | 9873 |
rs566056230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888452 | AAGTGGGAGGTGAGA[C/T]TCTATAGATAATAAG | 9873 |
rs566068447 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116750 | GCCATGTTGCCCAGG[C/G]TAGTCTCGAACTCCT | 9873 |
rs566079071 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990168 | GTGAAGGAAAAGGTT[-/A]AAAAAAACACAAAAT | 9873 |
rs566080150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905445 | CCAATTATACTTTTT[A/T]ATTTTTATTATACTT | 9873 |
rs566082682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115847 | ATTGAGGGTAGCCTC[C/T]TTTACTTAAAGTCAA | 9873 |
rs566095515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041962 | AGACAGAGTCTCACT[C/G]GTCACCCAGGTTGGA | 9873 |
rs566101422 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079959 | TACATTATTATATAG[C/G]ATTGTATAAACAAAA | 9873 |
rs566123665 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089602 | AATGTTATTCAGCCA[A/T]AAGAAAGAATGAAGT | 9873 |
rs566128530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991132 | ACTGATAAATTCCTC[A/G]ACACATACACCCTCC | 9873 |
rs566131241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963618 | GGAAGATAATTTTTC[C/T]ACAGATGGGTAGGGT | 9873 |
rs566137681 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977132 | ATTTCACCATATTGG[A/C]CAGGTGGTCTTGAAC | 9873 |
rs566140375 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977488 | AAACAACTCTATAGG[-/A]AAAAAAAAATCTAAT | 9873 |
rs566146045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123026 | TCCCATCAAAAAAAA[A/C]CACAAAATAATTAAT | 9873 |
rs566146128 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034884 | TGTCTGTCAACAACA[A/C]AACTGAAAATCCTCT | 9873 |
rs566149347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119959 | TTACAGTTCCACATG[A/G]CTGGGGAAGCCTCAC | 9873 |
rs566168842 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934095 | GCCTGGGCAACAGAG[G/T]AAGACACTGTCTCAG | 9873 |
rs566188784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081845 | AAATACTCAGAGCAT[A/G]GTACAAAGTAAGGAT | 9873 |
rs566199903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072058 | GACCAGGTAAACAAC[A/C]AATGAGTGAAGACAT | 9873 |
rs566205567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027786 | TGCTGCTCTGTGCAG[C/T]CTTGGGACACGGTGC | 9873 |
rs566213888 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926934 | AGAGTGAAAAAAATG[A/G]CGACTTGGTGCACTA | 9873 |
rs566251767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971597 | AGCACCTCTAGGAGC[C/T]GAGAATGACCCCAGC | 9873 |
rs566254652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057766 | TTTAAATCAGAGCTT[C/T]CCAAACAATGTATTG | 9873 |
rs566257098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965069 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 9873 |
rs566264426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072611 | AACAGGACACAGAAA[A/G]TAATACTCAATTTTG | 9873 |
rs566269176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003775 | ACAGGCGTAAAAATT[C/T]TATTTCACCAGGTTT | 9873 |
rs566278179 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127121 | TTATCACTAAAATAC[A/C]ATCAGGAGACATATA | 9873 |
rs566284323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72877407 | AATGGAAATATCACT[A/G]AGTATAGTCTTGTTC | 9873 |
rs566323890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064877 | TTAATAGCCTACCAA[C/T]TAAAAAAAGTCCAGG | 9873 |
rs566325813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073580 | CTTCACAATATTTTT[C/T]TTTTAGGATGGCTCA | 9873 |
rs566351352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023664 | ACAATCATGTTCTAG[A/G]TATTTGGCCAACTGA | 9873 |
rs566372738 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048783 | AGGGATGTATGTATA[A/G]TTCACCTCAAGAGAA | 9873 |
rs566393403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956135 | ATGGAGCAATTTGAG[C/G]GTAAAAATAAATAGT | 9873 |
rs566406976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093295 | TTAGCTATAATAAAT[A/C]ATAACCTTACTGAGT | 9873 |
rs566418113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105387 | TACAGTACACCCTCT[A/G]TATAAGACACCACCA | 9873 |
rs566420416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113000 | TACTTTCTAGATCTG[A/G]TAGGCGTGCTTCATT | 9873 |
rs566431974 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044273 | CAATTAAAAAAAAAC[C/T]TATGAATATTTCCAA | 9873 |
rs566438305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936313 | TATGTACTTGAGCAG[C/T]AGAACTGCTCTAAGT | 9873 |
rs566468563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085329 | CCAGGAATCTGACTC[C/T]CAGGCTAGGTAACAA | 9873 |
rs566478037 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016610 | GCAGCCAAACTCTCA[A/T]ATACCAGGAAAGAGA | 9873 |
rs566499344 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005608 | TCTAACTACATTCAC[G/T]CTGTTGAAAATTGTT | 9873 |
rs566507392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901106 | TTAAACAATTGCCAA[C/T]TGGGGCCGGACATCG | 9873 |
rs566540582 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107847 | TTTATCCATTTATCT[A/G]CTGATGGACACTCAG | 9873 |
rs566558413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030082 | TAGGTAAGAAATACC[C/T]AAGGGAATGCCATTA | 9873 |
rs566573282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965036 | CCTCATGATCCGCCC[A/G]CCTTGGCCTCCAAAA | 9873 |
rs566579881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967642 | ATGACAGCCAATGGG[C/G]TATAGAGCTTTTTTG | 9873 |
rs566591143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075688 | GGAGTGGTGGTGCGT[C/G]CCTGTAATCCCAGCT | 9873 |
rs566591431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901855 | TATTCCATTTATTAA[C/T]TCTATTCTGGTTTTT | 9873 |
rs566602321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914244 | GATCTTGAACTCCTG[A/G]CCTAAAGTGATCTGC | 9873 |
rs566634366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962296 | GTGATGATGCAATCG[C/T]TCTGACAGCTAATGA | 9873 |
rs566643733 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902028 | TACAGGGGCCCACGA[C/G]CAAGCCCAGCTAATT | 9873 |
rs566651688 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847733 | AGTCTCGCTCTGTCA[C/T]CCAGGCTGGAGCGCA | 9873 |
rs566653074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076580 | CAGGAGATGAACTGG[A/T]ATAATGGCAATGTTC | 9873 |
rs566654419 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937074 | ATCCAATAGCAAAGA[A/G]GAGTTCTTCCTTAGC | 9873 |
rs566656215 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868821 | ATATTCTCAAGGCTT[A/T]GTCCACATGCAGACA | 9873 |
rs566667686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134979 | CCTCCCAAGTAGCTA[C/G]AGTAGCTAGGATTAT | 9873 |
rs566669736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860688 | CATCTCTACTAAATA[C/T]ACAAAATTTAGCTGG | 9873 |
rs566679120 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045995 | TTTCAGTAATTTTTT[C/T]TTTTTTTTTTTTAGA | 9873 |
rs566680872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039082 | AATTGCAGAATCACT[A/G]TTTATTTTTATCTGC | 9873 |
rs566689812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141789 | GGGGAAGGGGCGCAG[A/C]GGTCGCCCCAGCCGC | 9873 |
rs566718093 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934822 | CCAAACTTTTTGACT[A/G]TTGGACACAAATTTC | 9873 |
rs566719135 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879930 | GTTGAACCCAGGAGG[C/T]GGAGCTTGACGTGAG | 9873 |
rs566724549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061562 | TAAGATCCACTGGCT[G/T]GAAATTCTCACTGCC | 9873 |
rs566725245 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103151 | GATGGAAATGTTCTA[C/T]ATATTGAGTGTAGTA | 9873 |
rs566733545 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142161 | GGAGACGGCGAGGGG[A/G]CGGGGGCCCCAGGAG | 9873 |
rs566767993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061203 | CTCACCTGGGAAGCA[C/T]AAAGGGTCAGGGAAT | 9873 |
rs566779153 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068980 | TGACTTCGCCACTGC[A/C]CTCTAGCCTGATGAC | 9873 |
rs566786272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053944 | TATTTTTTACTCATC[C/T]AATAATTCACTTTTA | 9873 |
rs566827853 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929340 | TATCTTTTTCAGCTA[C/T]CCAACACCCAGAATT | 9873 |
rs566827994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960223 | GGAGGGGAGATGCCA[C/T]GGCCAGTCTCATGTG | 9873 |
rs566829487 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945549 | CCAAAATTGACAAAT[A/G]GGATCTAATTAAACT | 9873 |
rs566843134 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862131 | CTTTAACATGATAAA[C/G]GGCATCTACAAAAAC | 9873 |
rs566857310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893615 | CCACTATGCCCAGCC[A/C]AATATTTTTCCTTTA | 9873 |
rs566870342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999670 | ATTCAGGTCTGAGAT[C/T]ACTTCATCAATGGAA | 9873 |
rs566896594 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944956 | GGAAGAATCAATATC[A/G]TGAAAATGGCCATAC | 9873 |
rs566906653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854441 | TCTACCTATCTGTCT[A/G]TCTGGTTAGAGACAG | 9873 |
rs566913373 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905520 | GGTATACATGTGCCA[C/T]GCTGGTTTGCTGCAC | 9873 |
rs566914526 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838406 | GATGAGAATCTTTGC[C/T]ACATCCTTGTGGTCA | 9873 |
rs566915416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938698 | TTTTACTCGTATTCT[A/G]CACAAACAGTAGAGA | 9873 |
rs566919751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846154 | TCCCAGACTACTCAT[A/G]ATGAGTAAGCTGCTC | 9873 |
rs566922829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892898 | TGTGAGCCACCGTGC[A/G]TGGCTGGTAATTTTT | 9873 |
rs566932580 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861635 | CAGTTCCAATCAATA[C/T]ATAGAAAGGATAGGC | 9873 |
rs566947150 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094876 | AAAATATTTTTTAAC[A/G]AGGCAAGCGGAACGA | 9873 |
rs566955209 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930670 | GAATTGCTAGAACCT[A/G]GGAGGGAGGCTACAG | 9873 |
rs566966443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057634 | CATTAGGCTCCATTT[C/T]CCTTTCAACATCAGT | 9873 |
rs566986544 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884100 | TTAAGAGACCACTCT[C/T]AGTATCATTAATAGC | 9873 |
rs567007364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993455 | CTATAGAGACACATG[C/T]ACACATATGTTTATT | 9873 |
rs567014258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009604 | TGATGAATTCCCTAA[C/T]CTTTTGCTTGTCTGG | 9873 |
rs567018117 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045469 | AAGACACATGCACAC[G/T]TATGTTTATTGTGGC | 9873 |
rs567023060 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997753 | TCATCCAGGCTGGAG[G/T]GCAGTGGCACGATCT | 9873 |
rs567028729 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048941 | CTCATTGCTATCAAA[A/T]TCTCACATGACAAAG | 9873 |
rs567043121 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139715 | GTGTAAAACCGTTAA[A/G]GTCAATAAAATGATT | 9873 |
rs567048318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985534 | GAGGCAAGCGTCAGC[A/C]AACTTTCAGGGCTGT | 9873 |
rs567054922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977926 | CCCAAATGCCCATCA[A/G]TGATAGACTGGATTA | 9873 |
rs567064875 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085632 | AAGGTGCAGGTTCAC[-/A]AAAAGACTTCAGAAG | 9873 |
rs567068757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993973 | TCTGTGAGTACGGTG[C/T]ATCCGGACATGTCCC | 9873 |
rs567084267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886402 | ATCTGCCAGCATTCA[C/T]CTTAAGTCTTCTTCT | 9873 |
rs567093725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025392 | ACGAATGCAGGAAAA[G/T]AAAACCAAATACCAC | 9873 |
rs567103811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955152 | ACTTCAGATGCTAAT[C/T]GGAAGTCTCAGGTTG | 9873 |
rs567119080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977236 | CCAAAACTATTAAAA[C/T]AAAGCATTGGGGGAA | 9873 |
rs567124578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141714 | CGCGCCCCCCACCTG[C/G]AGCCGGCGGCAAGTC | 9873 |
rs567135380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117430 | ATATTTTGGGTTTTT[C/T]CCTAATTTATTGAGA | 9873 |
rs567136720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934231 | CTTGTCTAGCATTTT[A/G]CATTTAAATGAGCAA | 9873 |
rs567153505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923488 | TGGTATTTTTTTTTT[A/T]AATTATGAAAGCCAT | 9873 |
rs567154980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042550 | ATTGAGGTCTTCTGC[A/G]GTTCCATACAATTTT | 9873 |
rs567158003 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891944 | TTACTTGAAACAAAA[A/G]TTTTCTTATTACTGT | 9873 |
rs567158451 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002926 | GAAAGCTCCATGAAG[A/G]CAGGGGTGTATGTCT | 9873 |
rs567166673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118798 | AACTCTGAGAGACCA[C/T]TATTACCATTTCTGT | 9873 |
rs567182418 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136511 | GAGATCACACCACTG[A/C]ATTCCAGCCTGGGCA | 9873 |
rs567187743 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878980 | CTGGTTTTGGTGGCG[G/T]GCACCTGTAATCCCA | 9873 |
rs567222266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935245 | GAATTAGGAGGGAAA[A/G]TGGGTCATTTTCCTA | 9873 |
rs567226003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070821 | ATAACTAACCAACAC[C/T]TCAGTGGTTAGTTAA | 9873 |
rs567229865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126116 | GGAGGCCGAGGTGGG[C/T]GGATCACAAGGTCAG | 9873 |
rs567230833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964270 | GGTTGATGGTTCCAA[C/T]CTTATGTTCTCATCA | 9873 |
rs567259543 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107583 | CATCCTCACTTCCCA[C/G]AAACACACACCCTCA | 9873 |
rs567261887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012256 | ACTCCTTAAGTGTGT[C/G]GGCGGGGAGCAAGGG | 9873 |
rs567271702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857526 | TCATTGCAACCTCTG[C/T]CTCTTGGGTTCAAGC | 9873 |
rs567272649 | in-del | -/T | 0.299487 | 0.245053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110155 | TAGTTTTCTTCTTTT[-/T]TTTTTTGATGTGTCT | 9873 |
rs567285006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097662 | CAATCCCTTCACTTG[C/T]TATTGAGAATTTCTA | 9873 |
rs567301100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956017 | TTGGGGAAATAGTTG[A/G]TTCCAGAATTGGGGC | 9873 |
rs567306163 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896248 | TGAAGATCTTGTTAT[C/T]TGCTGTTCAAAGAAG | 9873 |
rs567318659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849557 | GATTTGGGGAAAAAA[A/G]GAGTTCTAGGCAGAC | 9873 |
rs567319292 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042138 | CACTGTGTTGGCCAG[G/T]CTGGTCTTCAACTCC | 9873 |
rs567338214 | in-del | -/C | 0.00018615 | 0.00964575 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902669 | ATATCTTTAGGTCTT[-/C]TAATGAGGTTAAAAT | 9873 |
rs567349751 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090172 | TGTAAACCATCTTTT[C/T]ATATAAAAATGTTTA | 9873 |
rs567374565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889501 | TAATGCTTGAGCAAA[A/G]GAGTTTGAGACCAGC | 9873 |
rs567382720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035118 | ACTCCTGGACCTTGA[C/G]AAGTTATTTAACTTG | 9873 |
rs567394774 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096016 | CCTAAAGTGCTATAG[-/A]AAAAAAACAAAAAAC | 9873 |
rs567403889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996603 | ATAATTGTAATACAA[C/T]TGTGTTTATCTTCCA | 9873 |
rs567404209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105929 | TAAATAAGATACCTA[C/T]AGAAGATACCTGGCA | 9873 |
rs567410686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117977 | ATATATACATTTTCT[A/G]AGTTTTGACAAATGT | 9873 |
rs567413586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980771 | ATGTGTATGTATATA[C/T]ATACATCTCACTCTC | 9873 |
rs567415775 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039545 | AAAGAAAGAAAAGAA[A/G]TATTAATATGTCACA | 9873 |
rs567435333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957015 | AGAATCAAAGGACTC[C/T]AGTCTTTTTTTTTTT | 9873 |
rs567437698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927135 | GGTAGGCAAAAAACC[A/C]TGTAAGCCTTTAAGG | 9873 |
rs567439167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965688 | CATTTCCAACACCTC[A/G]GAAGGCACTCTTTCC | 9873 |
rs567442668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889228 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 9873 |
rs567447118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988906 | ATAGAGAACAAACTA[C/T]TAGCAACAATAACAT | 9873 |
rs567455114 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870230 | AATTCCTTTTTCTCT[A/G]CTCCTAAAGCACTCT | 9873 |
rs567455954 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873258 | CGCTTGAACCTGGGA[A/G]GTGGAGGCTGCAGTG | 9873 |
rs567473434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117356 | CCACACTCTTAAATA[C/T]TACATAATAATGCAT | 9873 |
rs567473486 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957939 | TGGAATTATATAAAC[A/T]TAAATTATTTTAAAA | 9873 |
rs567474713 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113290 | AAGGTCACATAGCTC[C/T]GTTTCTCCAGGACTG | 9873 |
rs567479069 | in-del | -/T/TTTTT | 0.481396 | 0.0946345 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959220 | ATATATCCAGCAGTC[-/T/TTTTT]TTTTTTTTTTTTTTT | 9873 |
rs567515127 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905009 | AACGTTTACTTCCAT[C/T]AGGAAGCTTGCTTCT | 9873 |
rs567533197 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914540 | CTAGTACAACAGACA[C/T]ATAGACCAATGAAAC | 9873 |
rs567548673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035377 | TCTCATCATGTTGCC[C/T]GGCTGTTCTCGAACT | 9873 |
rs567555025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981371 | CTTTAACTTCCTCTT[C/T]GCTTTAGGCAGAGAG | 9873 |
rs567568513 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851669 | AATTGCTTGAACCTG[A/G]GAGGCAGAGGTTGCA | 9873 |
rs567576985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927491 | ATGTAGGGGAAGGGA[A/G]TGTAAGGGAAATCTC | 9873 |
rs567580206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844436 | GTGGAGACTGAGCTG[A/C]TCCATTTGCGTGCTA | 9873 |
rs567581964 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973574 | CAACACTATCTATTG[G/T]CAGAGTGGTAGTTAC | 9873 |
rs567590743 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107320 | CCCAAAGTGCTGAGA[C/T]TACAGGCATGAGCTA | 9873 |
rs567590868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998314 | GGAGGCTGAGGCAGG[C/G]AGATCACTTGAGGTC | 9873 |
rs567600269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065967 | CTATCCCCATCAAGC[C/T]ACCACTGACTTTCTT | 9873 |
rs567606445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919552 | AATTTCCTCCATATA[A/C]AATGAACATGGTAAT | 9873 |
rs567616666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875216 | TCAATAATGGTAGAT[A/G]ATAGTATTTGCTACT | 9873 |
rs567624753 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139192 | TTTATCATTAACACC[A/G]GAGTTAATATTTTTC | 9873 |
rs567640456 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73013435 | TGGCTATCTCCTGTA[G/T]GCTTACAAAGGACAG | 9873 |
rs567641221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845051 | CCTAAAAAGTATCAA[C/T]ACGACCAGACGTTAA | 9873 |
rs567644795 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972459 | GGAAAGTAGAGGATG[A/T]CACAGGCAGGTATAG | 9873 |
rs567659452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990693 | ATACCAGAATCTCTG[C/G]GACACATTCAAAGCA | 9873 |
rs567661276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866828 | AATTTTCGTCAGTTT[C/T]GCTAGCAAGCCTGCC | 9873 |
rs567665031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918717 | TTTCAAATAAATGTA[A/G]AATAACATTGTTATT | 9873 |
rs567683460 | snp | A/G | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140402 | GTCATTCCATTTCAT[A/G]CACAAGCTCAATCCA | 9873 |
rs567687572 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021165 | TAAAGGTGCAGGCCA[A/C]TGTGTCTGGCCTATC | 9873 |
rs567707252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087017 | AACTGTAAAACAGCC[A/T]CAGGCAGTTCCTTCA | 9873 |
rs567709290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077747 | TTAATGCTAAATGAA[A/G]AAGCCAGCTGGGAGA | 9873 |
rs567723950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858533 | CAGAAGACCAAATAC[C/T]GCAAATTCTCATTTG | 9873 |
rs567746821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859361 | ATTTAGTGGCCATCT[C/T]GGTTATCCCAATTGA | 9873 |
rs567772902 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106289 | ACATAAACCTATATC[C/T]CCAGCATTCGGGAGG | 9873 |
rs567798628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913030 | AGCAGCTTTGTCTTA[C/T]GTGGCAGGAGCAGGA | 9873 |
rs567808812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014371 | TTGCCTCAAGTGATC[C/T]TTCCACCTCGGCCTC | 9873 |
rs567814300 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048982 | AACAGTAAATATTTA[A/T]ATAACAGAATCAAGA | 9873 |
rs567816148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059322 | AGGATTTTTACACTA[C/T]AAAGTTGTTTCCTTT | 9873 |
rs567817244 | in-del | -/AAACAAAC | 0.00239568 | 0.0345268 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855280 | AAAACTCCGTCTCAA[-/AAACAAAC]AAACAAACAAACAAA | 9873 |
rs567836027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960736 | AATGTTGGGAGTTGA[G/T]GTGGAGAAAGGGTAT | 9873 |
rs567836053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969284 | TTCTCCCTCTTGGAT[C/T]ATGTTAGAATGGTTT | 9873 |
rs567840977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951330 | GTGATGAAACAGATG[C/T]TGCAGATTGGGAAGC | 9873 |
rs567841954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862299 | ATAGGAAAGGAATAA[A/G]TAAAACTGTCTTTAT | 9873 |
rs567857546 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107239 | TTTGTATTTTTAGTA[A/G]AGACAGGGTTTCACC | 9873 |
rs567870649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900209 | CCTTCATTAACATGC[A/C]AACCCACACTTCCCA | 9873 |
rs567872270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961463 | GTCTCACTATGTTGC[C/T]CAGGCTGATATTGAA | 9873 |
rs567889543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950693 | AATTTGTAGTTTTTC[C/T]TTATTTCTTTTAGGA | 9873 |
rs567899426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998718 | ATAAAAAATATTAGA[C/T]TGCTTAATATCACCA | 9873 |
rs567899906 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075796 | AGACTGTCTCAAAAG[-/A]AAAAAAAAAAATCAA | 9873 |
rs567901134 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959396 | ACCATGCCCGGCTAT[-/T]TTTTTTTTTTTTGTA | 9873 |
rs567904713 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854564 | AGCCCCCCGAGTAGC[C/T]GGGACTACAGGAACA | 9873 |
rs567917668 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855112 | AACCCTGTCTCTACT[A/G]AAAATACAAAATTAG | 9873 |
rs567924014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943537 | TATTAATAGCTTTAA[C/T]GAAAGGGAAGGAAAT | 9873 |
rs567925198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109861 | CTTTTATTGTGTTGA[A/G]GTATGTTCCTTCTAT | 9873 |
rs567953165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043391 | TGGGCAACCTGTCAA[C/G]TAATGTATAATTTAA | 9873 |
rs567954294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890507 | TGCTCTTTCTCCAGG[C/T]TTCATATGAAAGATA | 9873 |
rs567954753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052075 | CACAGAACAAAGAAA[G/T]TTAGTGACATGTTTT | 9873 |
rs567957759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977128 | CAGCATTTCACCATA[C/T]TGGCCAGGTGGTCTT | 9873 |
rs567970972 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069822 | ACTCTGGGTACCAGC[-/A]AGGCAAATAAAACAT | 9873 |
rs567976151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870275 | ACAATGTGATAGGCA[C/T]GAAATTATACTTAGC | 9873 |
rs567983893 | snp | A/C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099134 | GGTAGAAGAATCACC[A/C/G]AGCCCAGGCGTTCCA | 9873 |
rs567987376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131660 | AGTAAGCCAAGATCG[C/T]ACCACTGCACTCCGG | 9873 |
rs567988608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110417 | CAAGGTTCAATCTTG[A/G]TAAGTTGTATGTGTC | 9873 |
rs567991949 | snp | A/G | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144432 | AGGCAGGAGAATAGC[A/G]TGAACCCGGGAGGTG | 9873 |
rs567997984 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139818 | GGTCCTTGTTTTTTC[A/T]GAATACTATGTGTGC | 9873 |
rs568002697 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940412 | AAGGAAATAATATAT[C/G]TAATGAGGTTAGTAT | 9873 |
rs568016320 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066548 | AAACTATCATCAGAG[C/T]GAACAGGCAACCTAC | 9873 |
rs568018249 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033207 | GCAGGAGAATGGCAT[-/A]AACCCGGGAGGCGGA | 9873 |
rs568020525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031826 | TTTTCGCCTGGAAAA[A/G]GCATATGCATTGCTT | 9873 |
rs568045108 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002294 | TATACCAGATGAATC[A/G]GTTTAGATGGAAATA | 9873 |
rs568080041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977738 | GGTGGGACTGTAAAC[C/T]AGTTCAACCATTGGG | 9873 |
rs568082796 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062978 | AGCAACCCTAAGACA[C/G]ATAATCGTCAGATTC | 9873 |
rs568102557 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069517 | TGATCACTAACAAAG[A/C]AATGGATAAGATAAA | 9873 |
rs568117260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915059 | TACAAGAAAGAAACA[A/G]ACAACTTCATTCAAA | 9873 |
rs568129260 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096885 | CTGAGTCTTTTTATC[A/T]TGAAAGAGTGTTAAA | 9873 |
rs568129286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016858 | AAACAGAATGTTTAT[A/C]TATAACAGGTGTCAG | 9873 |
rs568143852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062327 | AAATCCACAAAGATG[A/G]GGAGAAAGCAGTGCA | 9873 |
rs568144352 | snp | A/T | 9.88468e-05 | 0.00702948 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72887505 | CTCTAGCTTCATCTA[A/T]TTTCTGTTCTAGCTC | 9873 |
rs568147690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025242 | TGGAATCAACCTAAA[C/T]GCCCATCAGTGATAG | 9873 |
rs568171656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870967 | TGACTAACTTGTTTG[C/T]TGACTAACAGTAATG | 9873 |
rs568177923 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132460 | AGCAGAGCTGGGTTT[A/C]AATCTACGGCCTACC | 9873 |
rs568202185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113960 | CTCTTTGCTCAAGGG[C/T]CTAGGGCTCTACAAT | 9873 |
rs568202674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915684 | TTAGCCGGGCGCGGT[C/G]GTGGGCGCCTATAAT | 9873 |
rs568203042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909088 | GTCTCCCTCTGTTGC[C/T]GATACTGCCGTGATC | 9873 |
rs568211674 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953618 | CAGGTACTGGAGACA[C/T]TGCATGGGGGAAAAA | 9873 |
rs568248911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946141 | GGAAAGACTTGGAAC[C/T]AACCCAAATGTCCAA | 9873 |
rs568262463 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120660 | TTTCATCTTGGAAGG[C/T]GGAGGCTGCAGTGAG | 9873 |
rs568272351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026510 | TAAAATAAAAGAAAC[C/T]GAGTATAAAAATAAT | 9873 |
rs568278979 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999390 | AGTGGCACGATCTCA[A/G]CTCACTGCAATCTCC | 9873 |
rs568317151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010347 | ATTTTCTTGTATCTC[A/C]TTGAGCTTCTTTAAT | 9873 |
rs568317288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102742 | CCATGTGATAATGCA[G/T]CAAGAGCTTCCTCAC | 9873 |
rs568331375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954304 | GCCTCAAACACCTGG[A/G]CTCATGCAATTCTCT | 9873 |
rs568334904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027332 | GCTTTAACAGAGAGA[C/T]TGGCAGCATTTTGCC | 9873 |
rs568342491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840099 | CTCCAGCCTCCTAAT[C/T]GCTCCCTATATCCTT | 9873 |
rs568343620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129201 | TAAATTGATGTTCTC[A/G]ATTACAAAACAAATT | 9873 |
rs568347660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903514 | GTGAGCTACCGCGCC[C/T]GGCCTGGAATTTCTA | 9873 |
rs568348214 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018423 | TCTGGCCCTCTCACA[C/T]AACTCTATTTATGCA | 9873 |
rs568358276 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035782 | CTGGAGTACAGTGGC[A/G]CGATCTTGGCTCACT | 9873 |
rs568367513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055506 | AATAAGACAAAGTTT[C/T]AAACCTTGAGATACA | 9873 |
rs568396475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040742 | GGAAATATTTCAAAT[C/T]ATGTATTCTAATTAT | 9873 |
rs568401680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019116 | ATCTAAATGACATGA[C/T]AGTGACTTTTTCAGT | 9873 |
rs568416964 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946906 | GATGTAGGACAAAAA[C/T]GACTGCCTGCCAACA | 9873 |
rs568428887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987167 | GTGTGCATCTCCACA[C/T]CATCTATCAAATCAT | 9873 |
rs568435769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047072 | TATAAAAGACAAGAT[A/G]CAGAATAAATGTGAA | 9873 |
rs568439706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939587 | GGAAATCTATGAAGA[C/T]GGTTGATGGCTCTTT | 9873 |
rs568455477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025149 | CTGGGTACATACCCA[A/G]AGGAATATAAATCAT | 9873 |
rs568457091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033348 | GGAGGCTACCACTCT[A/G]GTCCTGTCCAAAGAT | 9873 |
rs568458888 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019926 | AAAGTTTTTAAAAAA[A/T]TTTTTTTCAAATCAT | 9873 |
rs568468753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135856 | TCGAAATTCCAAAAG[A/G]TAAGAACTGGGGATT | 9873 |
rs568474173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940238 | CACAATATCTAAATG[C/G]GGCTTTGTGTGTTTA | 9873 |
rs568480826 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840651 | AGCCATCATCTTGCA[A/T]TCTCACTGTGGCTCA | 9873 |
rs568498330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889703 | GGGTGACAGAGCAAG[A/C]CTCTTGTCTCAAATA | 9873 |
rs568508727 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843138 | ATAAAGAGTGCCTTG[A/T]TTCAGTCTTTACCAC | 9873 |
rs568533480 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130787 | GACCATAATATGGAA[G/T]TATATATTTACATTT | 9873 |
rs568537387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041101 | TTCCATTGTGTATAT[A/G]AACCATATTTTCTTT | 9873 |
rs568546650 | in-del | -/ATATATATAAAAGATCATATAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884569 | TTTATATATATGATG[-/ATATATATAAAAGATCATATAT]ATATATATAAAAGAT | 9873 |
rs568565328 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932866 | CAACAAATAATAACA[A/C]CAATCAGAATTCGCA | 9873 |
rs568571374 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125427 | TGCATGGTGTAGATC[A/G]AGTGTGGTGGCTCAT | 9873 |
rs568572903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863908 | ATGGTATAACCACTT[C/T]GGAAAACAGTTTGTC | 9873 |
rs568579159 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130165 | AGGTGTGAGCCACCG[C/T]GCCTGGCCCATAATC | 9873 |
rs568583775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890363 | GAGTAAAGAATCATT[A/G]AAGAGAAGTAAGAAC | 9873 |
rs568590032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080131 | TAGTAAGACCCTGTC[C/T]CTACAAAATAAAAAT | 9873 |
rs568598083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113146 | CAACTCCAGAATTTC[C/T]GCTTGATTTTTTGTA | 9873 |
rs568598657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034013 | AGACAATTTTAATAC[C/T]GATAGCAAATATATC | 9873 |
rs568609871 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102600 | CCATTATAACAGTAT[C/T]ACAAGCTGAGACTTT | 9873 |
rs568631298 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979960 | AATGTCCAGGAAATA[C/T]GAAAAGAACATAAAA | 9873 |
rs568652478 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920240 | GTCTGGTCAAAATAA[A/G]ACAGAGGGCACACAC | 9873 |
rs568653574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925629 | CAATAAAACATATAT[C/T]ATCTCATCATGAGAT | 9873 |
rs568659374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120030 | GCAGAAGGCAAAGAG[A/G]GAATGAGGAAGATGC | 9873 |
rs568665491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846510 | AAAGGCTCTCTGAGC[A/G]TCCCCATAACACTGA | 9873 |
rs568673291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029260 | ACAAGACTATTGTAG[A/G]AGCAAATTCTGAGAA | 9873 |
rs568708635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883693 | TCCCAGCACTCTGGG[C/T]GGCCAAGGCAGGCAG | 9873 |
rs568710473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864793 | TTGGTATGGCTTTTG[A/C]ATAAGAGAAGCAGGA | 9873 |
rs568711460 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039093 | CACTGTTTATTTTTA[C/T]CTGCAACCAGTTTCA | 9873 |
rs568714503 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980305 | TGAAACTGCTGCACT[A/G]GTTTCTCTATTAATT | 9873 |
rs568719740 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916948 | TGAGGTAAGGGTTCA[C/G]AACTTCATTGAACTT | 9873 |
rs568720079 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961524 | GCCTCCTAAAGTGCT[A/T]TGATTACAGGCGTGA | 9873 |
rs568727293 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920066 | AATATAGGATCTAAA[C/T]AGAAAAAGAAGCTTG | 9873 |
rs568760307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112289 | TAAAAGATTTCCCCT[C/T]TGGCACTTTAAACAT | 9873 |
rs568775607 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070382 | AGAACCTAGCATCAC[A/G]CCAGTCGTAAAGTAG | 9873 |
rs568782674 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956161 | ATAGTAAGAGTAACA[A/C]ATTTCAATCCATTGA | 9873 |
rs568786982 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072427 | TTTAATGAAGTTTTT[A/T]AAAACTTCCTTTAAT | 9873 |
rs568796700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023047 | GAGTTACACAAAAAT[C/T]GGCTCAAAATGATTC | 9873 |
rs568802203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844270 | CAGTGAAAATGCAAA[G/T]AACTATGTACGTGAA | 9873 |
rs568805338 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890436 | CTGCCCCAAGGCAGA[C/T]GGAACTCTTTAGAGG | 9873 |
rs568817586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111588 | TTGATTGAAGAGTTT[A/C]ATCCATTTACATTCA | 9873 |
rs568824813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099667 | CCCTGAGCAGTCAGG[C/T]GTTAGGCTTAGCGGC | 9873 |
rs568832686 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058114 | TCGATCTCCTGACCT[C/G]GTGCTCCGCCTGCCT | 9873 |
rs568841510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942708 | AAACATGCTATAGAA[C/T]GTTATGGTATATGCT | 9873 |
rs568847706 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936607 | TAGCAAGACTCCATC[A/T]CTAATTTAGAAAAGA | 9873 |
rs568859249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044174 | TAAATCAAACAAAGA[G/T]ACCATTTTAATAGAT | 9873 |
rs568875975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991029 | AAATGATAAAGGGGA[C/T]ATCACCACCAATCCC | 9873 |
rs568878613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943427 | GGTTTGAGTAGGAAA[A/G]GATTAGTGAGACACT | 9873 |
rs568882636 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035932 | CACCATGTTGGCCAA[C/G]ATGGTCTCAATCTCT | 9873 |
rs568905202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990420 | CTTCTCAGCACCACA[C/T]TGCACTTATTCCAAA | 9873 |
rs568912121 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998240 | CTAATTCAAGGTAGA[C/T]TGTAGTAAGTTAATT | 9873 |
rs568920425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037195 | AGTTCCCATGTATCA[C/T]TTGCCCCCACACATG | 9873 |
rs568923835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836297 | ACACAATTCATTACT[C/G]CTTAGGGTGGAGGTT | 9873 |
rs568929519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936194 | TTATTAAAATAATAG[G/T]GCTTAACCATTTCTA | 9873 |
rs568939818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982497 | TGTTTGGGTTTTGGG[A/G]AAACAGGAAAGAATG | 9873 |
rs568941095 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994660 | AGTCCCAGCTACTCG[A/G]GAGGCTGAGGCAGGA | 9873 |
rs568951636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061168 | CATGGAAGGCGAGCC[A/G]AAGCAGGGTGGGGGG | 9873 |
rs568954296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983131 | AACCCCGTCTCTACT[A/G]AAAATACAAAAAATT | 9873 |
rs568974951 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929191 | TAAACATACGTGTGC[A/G]TGTGTCTTTATAGCA | 9873 |
rs568976088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908422 | ATTGCTGAATCATAA[C/G]GCAGTTCTATTTTTA | 9873 |
rs568998199 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092310 | TTTTTTAAGTTTTTG[G/T]TTTTTTTTTTGTAGA | 9873 |
rs568999995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083805 | AATGTAAATCTATCA[A/G]CACACCTTCAAATAC | 9873 |
rs569001228 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929817 | TATTGAAACCATTTA[C/T]ATACATGTCAGATTT | 9873 |
rs569004335 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032685 | TAAAGCAGAGAGATC[A/G]AGTCAGGGAAGGCTT | 9873 |
rs569004417 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991609 | GGCTGGTTCAACATA[C/T]GCAAATCAATAAACA | 9873 |
rs569012854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052932 | GCTCACTGCAACCAC[C/T]GCCTCCTAGGTTCAG | 9873 |
rs569033485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875971 | GCCCAGCCCTCTGGC[C/T]AGTCCTCTAGCTGAA | 9873 |
rs569036480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100659 | TGAGCCACCGTGATC[A/G]GCCTACATACATTTT | 9873 |
rs569041078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970814 | TTGGGGTTAGGTATA[C/T]AAAATGGGACAAAAC | 9873 |
rs569043960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127856 | CTTTGGGTTGGGGGG[C/T]GGGGGTGGGAATCAC | 9873 |
rs569047846 | snp | C/T | 0.000166324 | 0.00911779 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867860 | TCCAAGAAAAGAAAT[C/T]GTACCGAGTGTAAAG | 9873 |
rs569058383 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967844 | TGCCTGTAATCTCAG[C/T]ACTTTGGGAGGCCGA | 9873 |
rs569061803 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084662 | GCCTCCCAAAGCATT[G/T]GGATTACTGGCATGG | 9873 |
rs569075316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076418 | ACCTCAAAAATATCT[A/G]CTAAGCGAAAGAAGA | 9873 |
rs569083537 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868372 | CGATGGGTGGGGAAG[C/G]AGAGCATTAAAAAGA | 9873 |
rs569088779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075532 | AATGATACAGTCAAT[C/T]TGGAAAACAGTTTGA | 9873 |
rs569097479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135015 | TGCGCCACCATGCAC[A/G]CCTAATTTTTGTATT | 9873 |
rs569102737 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008830 | AGCTACTTAACATTT[C/T]AGATATGAAGAGATC | 9873 |
rs569105420 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135830 | ACTGTATCATAATTG[A/C/G]TCTCCTCCCCTCGAA | 9873 |
rs569106780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974811 | AAAGAGGGCATTAAA[A/C]AAAAAAGGATATAAA | 9873 |
rs569116388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945487 | TCAGGACATAGGCAT[A/G]GGCAAGGACTTCATG | 9873 |
rs569138379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067989 | ACATGGTGACAGACA[C/T]GAGAGAATAAGAACC | 9873 |
rs569150467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067442 | ATGTAACAAAACTGC[A/G]CGTTCTGCACATGTA | 9873 |
rs569167163 | snp | C/T | 0.000153498 | 0.00875932 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73015821 | TACCTGTAATCATTC[C/T]GATCATCAGCTTTTA | 9873 |
rs569178338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015124 | GCTGGGATTACAGGC[A/G]TAAGCCACTGCCCCT | 9873 |
rs569183561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957232 | TATTCCCCTTCCTGT[A/G]TCCATGTGATCTCAT | 9873 |
rs569194244 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966627 | ATTCCTGCATGAATA[C/T]ATTCAACAGATATAT | 9873 |
rs569195085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959049 | TGCGTGCATGGGACA[C/T]ACATCTCCTTACATA | 9873 |
rs569197266 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961757 | TAATCACATGTCAAG[A/G]GAATCATCAATAGTC | 9873 |
rs569208960 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143127 | GGCGGCACTCTACTG[A/C]AGGGCATTCAAGTCA | 9873 |
rs569228882 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875393 | TATTTGACAGAGTCT[C/T]GCTCTGCTGCCCAGG | 9873 |
rs569232219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967581 | AATTCAGAGACAGAA[A/G]GCAGATTAGTGGTTG | 9873 |
rs569236777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086214 | AGGAGTTTAAGACAG[G/T]CCTGGCCAACATGGC | 9873 |
rs569237649 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934388 | AGGCTGGTGTGCAGC[-/G]GGCACTATCTCGGCT | 9873 |
rs569239313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952078 | CTGCATATGTCTTAC[C/T]AAATGAAGACAAGAT | 9873 |
rs569264935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860388 | GTTTATACTGGGTTA[C/G]AAAACAAAGCTCAAA | 9873 |
rs569275023 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852704 | GCACGTGTATATTCA[C/T]TGCAGCACTATTTAT | 9873 |
rs569276374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861148 | CATATAATTAATAAA[C/T]CTCTAGCAGAATGAT | 9873 |
rs569278371 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142218 | GGGCGGCGGGTTAGC[C/T]GCAGCCGCGTTGTCC | 9873 |
rs569288975 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063198 | TAACTAAGCTTCATA[A/C]GCAAAGGAGAAATAA | 9873 |
rs569297352 | in-del | -/AAA | 0.00451692 | 0.0473081 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049873 | GCACAAAAGGACCAT[-/AAA]AAAAAAATTGTTTTC | 9873 |
rs569298600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900307 | AGAGCTCAATATCCA[C/T]CAGTTGGGCGGCTTT | 9873 |
rs569311623 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903465 | ACCTCGTGATCCACC[A/G]GCCTCGGCCTCCTAA | 9873 |
rs569328449 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846085 | AGATAGATAGATAGA[C/T]AGATAGATAAGTAGT | 9873 |
rs569346616 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902834 | TGTCCTATTTTCTCA[A/C]AAATAAATTTGGAAA | 9873 |
rs569348568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108411 | GCTTTTTCACTTCAT[A/G]TAATCCTATTTGTTC | 9873 |
rs569349502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064050 | TGAAAGTAAAACACT[C/T]CTCAGCAAATGCAAA | 9873 |
rs569351360 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912457 | TTGAACCATCCCTGC[A/G]TTCTTGGGATACATT | 9873 |
rs569352243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101592 | ACAGATGCACATACC[A/G]TGCCCAGCTAATTTT | 9873 |
rs569369595 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100750 | CGCAGCTTGGATGTG[G/T]TAATGTTGAAATTCG | 9873 |
rs569386078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045214 | AAATTAAAACCACAA[C/T]GAGATACCATCTCAC | 9873 |
rs569412648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108881 | CAGCCTAGATTTAAG[G/T]TTTTAACACAATTTG | 9873 |
rs569413279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056736 | TACTACAGGAGAGCA[C/G]ATGAGAGCCATCAAA | 9873 |
rs569413623 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910282 | TGGGAAGTGAGGAGC[A/G]CCTTTGTCCGGCCGC | 9873 |
rs569432631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093465 | GGTATTAGGGATTCT[C/T]GAACTTACAGCTGGT | 9873 |
rs569433531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112214 | TTTTGTTTGTCTGGA[A/G]AAGCCTTTATTTTTC | 9873 |
rs569449605 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891490 | TTGGGGTTATCAGAA[A/G]TTTGGGAATGAACTT | 9873 |
rs569451567 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853770 | TGCATCAAAGAACAA[C/T]AGAGTGAAAAGACAA | 9873 |
rs569452200 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964875 | GCTCACTGCAAGTTC[C/T]GCCTCCCGGGTTCAC | 9873 |
rs569456432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985264 | AAAACCAAGAGTAAT[C/G]ATTATTTTCCTTTAT | 9873 |
rs569463830 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892681 | ATGATCTCAGCTCAG[C/G/T]GCAACCTCCACCTCC | 9873 |
rs569466177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000478 | AAAATATGTCCATTT[A/G]AAAACATTTACTCAT | 9873 |
rs569467213 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029845 | AGGCACAGGCTCAGA[A/G]AATTCCTGAGAAGAC | 9873 |
rs569467634 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038168 | AGGCAACAAGGAGAT[C/G]TGTCTCTATTAAAAA | 9873 |
rs569485095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948077 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 9873 |
rs569499559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885189 | CCCTCATATTTGCTG[A/G]CTAATTTTACTTAGG | 9873 |
rs569512149 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888132 | AACAAGATAGCCAAG[C/T]ATAGGAATCTGAGAA | 9873 |
rs569514783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096709 | TTCACCACTGAGTAC[A/G]ATGTTACTGTGAGCT | 9873 |
rs569522789 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948727 | CTGGAGTGCAGTGGC[A/C]CAATCTCGGCTCACT | 9873 |
rs569528182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992979 | AACAGGCAACCTACA[C/G]AATGGGAGAACATTT | 9873 |
rs569533678 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921729 | TTTGTTCGTTAATGC[A/T]TTCTTCTAATATCAC | 9873 |
rs569538658 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943136 | AGCTAGGATTACAGG[C/T]GCGTGCCACCATGCC | 9873 |
rs569570999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909876 | AGTGCCTCTGCCCGG[C/T]AGCCGCCCCATCTGG | 9873 |
rs569607790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903762 | GCAGAAGAAAAAAAA[A/G]GTTCAAAGTAACTCT | 9873 |
rs569609253 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941743 | CATACACTGCTTTCA[C/G]AAGTATATACTGATA | 9873 |
rs569610791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071763 | GGAAATGGACAGAGT[A/G]AAACACAGGTTTCTT | 9873 |
rs569618032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848615 | CCCCCAGTGTATCAC[A/G]TATTGGGCACTCTAT | 9873 |
rs569620162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118224 | CTTGGGAGGCTGAGG[A/C]AGGAAAATTGCTTGG | 9873 |
rs569627918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111326 | ATATTTACAACTGTT[A/G]TATCTTCTTGCTAAA | 9873 |
rs569630454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970753 | AAAAGACTTCCATGA[A/G]GAAAGGCCGCTGAAC | 9873 |
rs569639019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019047 | AAACAAGTGGCAAAA[G/T]GTGATATAAGTACCC | 9873 |
rs569670246 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138900 | GGTGTCAGTGACTGC[A/G]CACGGCCTCGCATAG | 9873 |
rs569674491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864607 | TTGTTTGTCAATTAA[A/G]AAATAAATAAATAAG | 9873 |
rs569675250 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885214 | TTAGGCTATTTTTTG[-/T]TATCTGTTAAGTGGA | 9873 |
rs569681964 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963408 | TGAGCTAAGTGAGGC[A/C]TACAGAAGGGAAATA | 9873 |
rs569690360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910254 | AGGAGAGCCTCTGCC[C/T]GGCCACCCCATCTGG | 9873 |
rs569707734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090751 | ATGTGCATATATATA[A/G]TGCATGTTTTTATTG | 9873 |
rs569735489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011381 | GGAACATGTGCACCA[C/T]CTAGGCTAGCAGGTG | 9873 |
rs569749918 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017044 | CTGGAGTGCAGTGGC[A/G]CGATCATGGCTCAAT | 9873 |
rs569770576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082623 | ATGCCCCAATCTCTC[A/G]TTATTTATAATGAGA | 9873 |
rs569786279 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038400 | ATTGATTCTTAAAGG[G/T]ACCTTATAATTTATC | 9873 |
rs569787141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041468 | GTTTTGATTTTCATT[C/T]CCCTGATGATTAGTG | 9873 |
rs569805158 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842282 | CTAAGAGTTTTACTA[C/T]GTAAATTAACCACAG | 9873 |
rs569812244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849396 | AAGATTAAGTTTGGC[G/T]GAGCAGAAGTGCTAT | 9873 |
rs569827877 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057064 | CTCTAGCCTGGGCGA[A/C]AGAGCAAGACTCCGA | 9873 |
rs569842094 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865866 | AAGTGTGCTACACAG[C/T]AGTCCAGTCATACAC | 9873 |
rs569847493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72933588 | GATACCCAACTTATA[C/T]TAGCCATATCCAAAT | 9873 |
rs569852212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896629 | AAAAGTCCCAAGGGA[C/G]TTTTAGTGATCAATC | 9873 |
rs569854738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137552 | CATTCGACAACAAGG[A/G]TATAAAGATACAAAA | 9873 |
rs569858287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003384 | GTAACAGCAGCAGAA[C/T]TGTAACAAATAGAAG | 9873 |
rs569861872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880940 | ACTAGTACAAGAAAA[C/G]ATAGGGGAAATGCTT | 9873 |
rs569864300 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846900 | TAGAAAAACTCTTGA[C/T]GAAAATTTCAGTAAG | 9873 |
rs569868031 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973418 | GGTAAGTTATTTATG[-/AT]ATATATATATACAAT | 9873 |
rs569885893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996486 | AAAAGCCTTAAGTTA[C/T]TGTAGCTCTCATTCT | 9873 |
rs569892558 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090435 | TTTCACCGTTTTAGC[C/T]GGGATGGTCTCGATC | 9873 |
rs569894186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850643 | CAGGTGTGAGCCACC[A/G]TGCCTGGCCAGGACA | 9873 |
rs569902323 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122846 | ATAGTGTGGCTGTTC[C/T]ACTACATTTACAAAG | 9873 |
rs569906138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866626 | ACCCCAAAGTCAAGT[A/G]GGTGATGTTTCTTTT | 9873 |
rs569911157 | snp | C/G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093431 | CCTCCAACCTTGAAG[C/G/T]TGGTGTCAAAGTGAA | 9873 |
rs569916280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136898 | TTAGCCGGGCGTGGT[G/T]GCAGGTGTGGTGGCA | 9873 |
rs569920150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858409 | AAAGAAAATGTGGTA[C/T]ATATACACCATGGAA | 9873 |
rs569931955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042100 | CCCAGCTAATTTTTT[A/T]ATTTTTAGTAGAGAC | 9873 |
rs569939928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888594 | TTAGAGTTTAGTCTT[C/T]GAGATATATTTTCTT | 9873 |
rs569954067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115741 | GAGATAGGAGTTGAT[G/T]CTGCAGTCTTGAGGC | 9873 |
rs569965203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934205 | CACGTATGATGAAGA[C/T]GCATCTGTATCTTGT | 9873 |
rs569982563 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144269 | GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCCGAG | 9873 |
rs569982656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004910 | TTTCAGCCAACAGTG[A/G]CACTATCAGAAGGCA | 9873 |
rs570007396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072815 | GAAATTCACCAAAAA[A/G]GAACCCCCACCACAT | 9873 |
rs570015619 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839367 | GTTTTTGGTGGATTT[G/T]AAGCAATATCAGATC | 9873 |
rs570020991 | in-del | -/GT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051815 | TTCAAATAAGTATTA[-/GT]GTTTTCAGGCTTTTT | 9873 |
rs570027904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035044 | GATTCTGATATGCAG[C/T]CACTATTGGGAACAA | 9873 |
rs570031248 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083860 | AAGGACAATATTTTA[G/T]TCATCTTTATGTGCT | 9873 |
rs570031472 | snp | C/G | | | missense, synonymous-codon, nc-transcript-variant, intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842629 | CAGGTACCTGAATCT[C/G]TCTCATCCATGGAGT | 9873 |
rs570041727 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977028 | CTTCCCGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 9873 |
rs570044903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005857 | GTTTTAAAGCCATCC[A/G]GTCTCATGGCTTTAA | 9873 |
rs570044940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997523 | AAAAACCGCAGGCGG[A/T]TAAAAGAGACCTACA | 9873 |
rs570046413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927424 | GTGTAGGTTCATCAA[C/T]TGCAACAAATGTGCC | 9873 |
rs570066566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874182 | CTTGCCCTAGCACCA[C/T]TGTAGTATGCTTTTG | 9873 |
rs570070647 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087726 | AAAAAAAAAATTTTT[A/T]AAATAAATTTAGTGC | 9873 |
rs570073197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875156 | GGACAAGGACTGTGT[A/G]TAATGTATTACTATT | 9873 |
rs570085312 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116966 | CAAAAAAAATCACTA[C/T]TGTTATATCTCTGTT | 9873 |
rs570093633 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850828 | TGTGTGGTGGCTCAC[A/G]CCTGTAATCCAAGCA | 9873 |
rs570105252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093779 | GCTAATTTTTTTTGT[A/G]TTTTTAGTAGAGACA | 9873 |
rs570112067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130040 | CACCCGCCACCACGC[C/G]CAGCTAATTTTTTTT | 9873 |
rs570114906 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947911 | ATTTTAATCAGTTAA[C/T]ACAGTGTTAACATTT | 9873 |
rs570142990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028457 | AAATGCCTGTACCCC[C/T]ATTGTATCTTGGAAG | 9873 |
rs570150839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976168 | AAATCTGCCTAATAA[C/T]ATACAGACAGAGAAA | 9873 |
rs570172851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021034 | GGTGCATGCCACTGC[A/G]ACCAGCTAAGTTTTA | 9873 |
rs570188515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873101 | TCGGGAGGCTGAGGC[A/G]GGCAGATCACCAGGT | 9873 |
rs570193344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965096 | GCCTGGCCAATCATT[C/T]TACTTCTTAATTCAA | 9873 |
rs570205072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911525 | ATCTCTGTGAAGAAT[A/G]GCACTGGTATTTTGA | 9873 |
rs570220088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014238 | CTGGGCTCAAGCGAT[C/T]GTCCTGCCTTAGCCT | 9873 |
rs570237505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976798 | CTAAGAACATACACT[A/G]GGGGAAAAGTGCTGG | 9873 |
rs570243606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869573 | CTTCACGAATTTGTG[C/T]GTCATCCTTGCATAG | 9873 |
rs570274903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956845 | AAAAAAAAACCAACC[C/T]TAGAAGACACCAAAT | 9873 |
rs570283915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912174 | AGCTAGGACTTCCAG[C/T]ACTATGTTGAACAAC | 9873 |
rs570285547 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995671 | TTCATGCCACTGCAC[G/T]CTAGCAGGGGTGACA | 9873 |
rs570289293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905888 | ATTGTGAATAGTGCC[A/G]CAATAAACATATGTG | 9873 |
rs570293033 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012703 | GGGAGTCATTGTATA[A/C]TTCTTCATCTCTCTC | 9873 |
rs570301976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058424 | GCCCATCAATTATCT[A/G]AACAACAAACTGACT | 9873 |
rs570305770 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870129 | TTGATGCCTGGTGAG[G/T]GCTTATCTTTTGACG | 9873 |
rs570317878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862246 | CTCTCACCACTTCTA[C/T]TCAGCAATTTTATAG | 9873 |
rs570318515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937616 | CCAAAGTGCTGGGAA[C/T]ATAGGCGTGAGCCAC | 9873 |
rs570330823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887128 | ATTGATATATAAGGA[A/G]ATATATATATATATC | 9873 |
rs570354361 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021753 | CAGAATTCTAAAAAA[A/T]CTAGATGCAGAAGAA | 9873 |
rs570361654 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892804 | AGAGACGGGGTTTCA[A/C]CATGTTGGCCAGGAT | 9873 |
rs570375055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898391 | TGTAAGGCAAGGGCA[C/T]ATGCAAAGTATATGT | 9873 |
rs570382455 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064822 | AAAGAAGTCGAATCC[C/T]TGAATAAACCAATAA | 9873 |
rs570404938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086167 | AATCCCAGCACTTTT[A/G]AGAGATAGAGGTGGG | 9873 |
rs570416248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038110 | AAAAATTCTTATGAC[A/G]AGGTGGGAAGATTGC | 9873 |
rs570434062 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958904 | CCATTTCCATCTATG[A/G]AAACAGAAGCACTGG | 9873 |
rs570441726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000654 | CAAGAACTAGTGGGA[C/T]TAATAACCTTGTAAC | 9873 |
rs570475349 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031042 | CTTAAAAAAAAGGGA[C/G]ATCCTGCTATTTGTC | 9873 |
rs570480630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076701 | TATGTAAATTAAAAG[C/T]ATACATAAAAGTATT | 9873 |
rs570502752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001347 | GGGAGTTCTGATTCA[C/T]TAGTTATTCTTAATA | 9873 |
rs570503484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023743 | AGCTTTATTGATAAA[C/G]TTGGCAACAAAGATG | 9873 |
rs570510605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115641 | CAGACAGACATAAAG[A/G]TATTTATTTTAAGAA | 9873 |
rs570514493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968224 | TACAATGTAGATGCT[C/T]CAAAATTACTTTCTG | 9873 |
rs570518971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930870 | GAATAAGACCTACTA[C/T]TTGATAGCACAATAG | 9873 |
rs570527802 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034995 | ACTCTAGAGGTGGGG[C/T]TGAGACACTGATAGT | 9873 |
rs570538667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031677 | AACCAACACTGCTTA[C/T]ACCCAGGAATCCAAC | 9873 |
rs570558210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914275 | CCACCGTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 9873 |
rs570560561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016730 | AAGACAGATTTTAAG[A/G]GTCTTTTCTTTTTAA | 9873 |
rs570586868 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089066 | AATTTCCTGTTTTAA[A/G]GCAAAAGACAAATCT | 9873 |
rs570589661 | in-del | -/AT | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836470 | CCTCCCTTCTAGCAC[-/AT]GTCCCACAGTACTGT | 9873 |
rs570595382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923132 | ATTCCTTTTTACAGC[G/T]TAATAATATTCAGTT | 9873 |
rs570600806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039887 | ATCATTTTGAAGTTT[A/C]TTTTTAAATTTTCAT | 9873 |
rs570602438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960593 | GTTCCATGCAGCTGC[C/T]ATTAATTTCTTACAA | 9873 |
rs570619426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886466 | TTTCTGTGGCCTCTG[G/T]GTTCTTCAACTATAC | 9873 |
rs570637642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069172 | AAAAATTAGCCAGGC[A/G]TGGTGGCATGCACCT | 9873 |
rs570646905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115079 | CTGCAGTGGCAAGGC[A/G]TGCTGAAATTCAAGT | 9873 |
rs570661186 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033011 | GTACTTAGATTGGCC[A/G]GGTGCGGTGGCTCAC | 9873 |
rs570663796 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032808 | ATACAAGCTGGCATG[C/G]AGCTTGTAAAAGGGA | 9873 |
rs570665815 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974953 | TACAAGAGCTAGAGA[A/C/T]GACAGAGAAACCAGA | 9873 |
rs570680269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914889 | ATTGACAAATGGGAT[C/T]TAATAAAACTTAAGA | 9873 |
rs570698651 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061705 | GCCTCTGGGAAGTTC[A/G/T]AACTGGGTGGAGCCC | 9873 |
rs570700674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901920 | CACTCTGTCATCCAG[A/G]CTGGAGTGCAGTGGT | 9873 |
rs570717496 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924220 | AGCTGGGACCACAGG[A/C]ACTCACCACTGCATC | 9873 |
rs570724350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054028 | GTCCTCACAACAGAT[A/G]GTTTGAGTGCACAGG | 9873 |
rs570725742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033266 | GCACTCCAGCCTGGG[C/T]AACAGAGCGAGATTC | 9873 |
rs570731317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054892 | GAGGACTGCTTGAGA[C/T]CAAGAGGTTGAAGCT | 9873 |
rs570735377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846810 | GAAAATATGCATAAT[G/T]GAGCTCTTACGGTAC | 9873 |
rs570739886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961308 | AGCTCACTATAGCCT[C/T]GAACTCCTGGGCTCA | 9873 |
rs570743155 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953015 | ACTTTGACTTGAAAA[A/G]ATTTTGTTACTGAAA | 9873 |
rs570743168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121751 | TATAATTTATAACAG[C/T]GGTCCACAAACTTTA | 9873 |
rs570771448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062232 | GCCTGTCAGAAGGAA[A/T]ACTAACAAACAGAAA | 9873 |
rs570773406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909301 | CTCGGCCTCCTGAGG[C/T]GCTGGGATTGCAGAT | 9873 |
rs570777213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024843 | AAGGACATGAACAGA[C/T]GCTTTTCAAAAACAG | 9873 |
rs570782310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046101 | ACTCAAGGGATACTG[C/T]GGCCTCAGCCTCTGA | 9873 |
rs570788898 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912739 | TAAAATTCAGCAGCA[A/C]AGCCACCCAGTCCCA | 9873 |
rs570790346 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091604 | GACAGAATTATAGAA[C/T]GTCAAACCACATTCA | 9873 |
rs570792588 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021982 | GTGTATGGCAGGAGA[A/G]GGAGAGGAGAATGAG | 9873 |
rs570806242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120721 | GCAACAACAGCAAAA[C/T]TGTGTCTAAAAAAAT | 9873 |
rs570812123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902822 | TTATTATTTATCTGT[C/T]CTATTTTCTCAAAAA | 9873 |
rs570827628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934823 | CAAACTTTTTGACTA[C/T]TGGACACAAATTTCT | 9873 |
rs570830672 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945653 | GCAATCTACTCATCT[G/T]ACAAAGGGCTAATAT | 9873 |
rs570837587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939485 | GAGTTATAGAGATTT[A/C]TTCAGATGTTAAAAG | 9873 |
rs570855982 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052111 | GAAACTTAATAAATG[C/T]AAAGATAGTATGGCA | 9873 |
rs570864224 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081175 | GCACTGTGGCTCATG[C/T]CTGAAATCCCAACAC | 9873 |
rs570866353 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986386 | AGCTAATTTTTTGTA[G/T]TTTTAGTAGAGACGG | 9873 |
rs570866991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129463 | AGCAGCATTAGATTC[C/T]CATGGCACGAACCCT | 9873 |
rs570869962 | in-del | -/TTTG | 0.00120651 | 0.0245316 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901872 | TATTCTGGTTTTTTT[-/TTTG]TTTGTTTGTTTGTTT | 9873 |
rs570870808 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847709 | TTTTTTTTTTTTTTT[C/T]TGAGACAGAGTCTCG | 9873 |
rs570890950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73103411 | CTGCTTCCATTTTTA[C/T]AAGATTTAATTAGAC | 9873 |
rs570894222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897422 | GGACCATTATTAGCA[C/T]AGCATTTACATTGTA | 9873 |
rs570894555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135894 | GCGTTGCAGCAGTAG[C/T]GGCTCATTTCTGTAA | 9873 |
rs570898083 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839132 | TCCTATGACTAAGAT[C/G/T]CTAGCACATCCTCCA | 9873 |
rs570900044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946070 | CAAAGGATTATAAAT[C/T]ATGCTGCTATAAAGA | 9873 |
rs570900072 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025666 | TAAAAATTAAATAAA[C/T]AGAATTTTAAAAATT | 9873 |
rs570910303 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846417 | GAACTCCTGACCTCG[C/T]GATTCGCCCGCCTTG | 9873 |
rs570913494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046984 | TGATGCTGTCAATAA[A/T]ATGAGGTCTTTCTGT | 9873 |
rs570925420 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932155 | ACATACTGTTAATTA[C/G]CAAATCTTATTGATT | 9873 |
rs570926266 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094976 | TCTAACATCCATTGA[A/C]TATCTTCTGGATTTC | 9873 |
rs570933947 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138713 | TACTAGGTTCAAGCA[A/G]TTCTCTGCCTCAGCC | 9873 |
rs570937079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980341 | TCATGAATCTGCTCC[A/G]TCGAAACTTTTCTTC | 9873 |
rs570938375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994582 | ATAGTGTAAACTCAC[A/G]GTGAAACCCCGTCTC | 9873 |
rs570951848 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143253 | TTTCTAAAGGTTACA[C/T]AGCAGGACTAGAATC | 9873 |
rs570990869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871164 | CGATCAGAAAGTAAC[C/T]GCTGCTTTGCTCCAA | 9873 |
rs570993357 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940127 | AATTCCATAGAAGCA[A/G]GACAAATAAAATTTA | 9873 |
rs570998273 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017067 | GGCTCAATGCAGCCT[C/T]AACTTCCTGGGCTCA | 9873 |
rs570998702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042746 | TTCATCAGTGTTTTG[C/T]GGTTTTTTGTTGTAG | 9873 |
rs570998727 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976230 | GGCATAAGAAATAAA[C/T]AGTATTTCTTGGGGA | 9873 |
rs571009000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079864 | CCAAGCAGAGACACA[C/T]TGGAGTATTTTAATT | 9873 |
rs571024610 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955223 | CTATGACACCTTTCT[C/T]AGGGTCGATTAGTTT | 9873 |
rs571033774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026370 | ATTACAGTTGCTCTT[A/G]CCACTGGGAGCAAAA | 9873 |
rs571049281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087857 | ACTTCCAGTCTCCTA[A/G]GCTCCATTCATGGCA | 9873 |
rs571055176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978103 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA | 9873 |
rs571059348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879891 | GTAATCCCAGCTACT[C/T]GAGAGACTGAGGCCG | 9873 |
rs571060441 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035429 | CACCTTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 9873 |
rs571071138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071327 | CATTTTCCCAAAAAG[C/T]ATGATTTCCAACCCC | 9873 |
rs571072019 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086453 | TCAATCTCAAATCAA[A/C]AGCCTAACTTTACAA | 9873 |
rs571082990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990670 | ACCAATGAGAACAAA[C/G]ACACAACATACCAGA | 9873 |
rs571084851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952160 | TTAACTTATATTGGT[C/G]TTGCTTGGTCACTCA | 9873 |
rs571091069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978966 | GGTTCAAGCGATTCT[C/T]GTGCCTCAGCCTCCC | 9873 |
rs571098883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018458 | CATCATACACTGTTA[C/G]TGTCTGGTTTAAATA | 9873 |
rs571117273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927716 | GCACAGTTACTTTAG[C/T]TGACTAGGTTGAGCA | 9873 |
rs571124047 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941963 | TTAATGGCATATTAA[C/T]ATGATCAAATACTAT | 9873 |
rs571137650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080750 | GCAGTTCAAAACCAG[C/T]CTGGACAACATTGTG | 9873 |
rs571144644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72996752 | ATCAGACTACCTTTC[C/T]CTAGACTGGAAAGTG | 9873 |
rs571150248 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986684 | TGCATGTAGATCTTC[C/T]AATATAAGGTTTTAA | 9873 |
rs571161180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027163 | AAGAGAGGAGGATGT[A/C]GGAAAGTTTGGAACT | 9873 |
rs571187501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970070 | AGAATACCAGTAAAA[A/T]GAACCCAACTTGCTG | 9873 |
rs571192189 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048903 | AACGACCACACAAAC[A/G]TAGCAAGATGTTGAT | 9873 |
rs571195619 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837888 | GCGTCCCCAGTAGAG[A/C]AGCTCAACAATGCAG | 9873 |
rs571196435 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118137 | CAGCCTGGCCAACAT[-/G]GTAACACCCCATCTC | 9873 |
rs571204644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928368 | TCTCATTAGCACCAT[A/C]TCTCATCACTGTTCT | 9873 |
rs571211406 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004767 | TTTAAATTGATGTCA[A/C]ATAAATGCTAGTAAC | 9873 |
rs571218605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956781 | TGGGGAAACTTCAGA[C/T]CATAGCACTATTGCA | 9873 |
rs571222857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106501 | AAAGAACCCTGAAGT[A/G]CAAACTGTTACAGGA | 9873 |
rs571228015 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106051 | ACTGGGATGAACTTT[A/G]GAAATTATGTGGAGA | 9873 |
rs571230289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077791 | GACACACAGGAAAAC[C/T]CTGGGGGCTTACAGA | 9873 |
rs571242828 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919822 | ATTAGAATAAATGTC[A/G]TTGGATTAAAAATAC | 9873 |
rs571267844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997991 | AACTACCACTCCCGT[C/G]CCCAAAAGATGAGTT | 9873 |
rs571276243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125270 | CTTTTTAAAAGATAC[C/T]TGTTTAAAGAAAACT | 9873 |
rs571298552 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952329 | CCAAGTTTGACTATC[-/T]TTTTTTTTTTTTTGA | 9873 |
rs571299177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942629 | TGTACTTTTCAAATT[C/T]TCTTCTGGTACTTTG | 9873 |
rs571321824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943290 | GACCTACTTTGCCCA[A/G]CCCTGACTTTTATAT | 9873 |
rs571328364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889544 | GCAAGACCCTATCTC[C/T]ACAAAAAATCTAAAA | 9873 |
rs571329020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117159 | ACTTATAACAAATAC[A/G]TTCTACATGTACTAA | 9873 |
rs571329958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990340 | GCATCAATTTGGGAT[A/T]AACTAAAAATTAACT | 9873 |
rs571333497 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098491 | CTGGAAAATGTTTTA[C/T]GTGTACTTGAGAAAA | 9873 |
rs571344661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082893 | ACAACCATAAAATGA[C/T]ACATCAACATAATTT | 9873 |
rs571355456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067269 | TCTCACTCATAAGTG[A/G]GAGTTGAACAATGAG | 9873 |
rs571366013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028703 | CAATTCTCAACTGGA[A/G]TTGTAATCCCCATGT | 9873 |
rs571368758 | in-del | -/G | 0.00558655 | 0.0525553 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089972 | TAATTAAAATAGCTT[-/G]GTAATGGAACATAAG | 9873 |
rs571383553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883033 | TAGTTGTTTTCAATA[C/T]GGGTGCAAAGGTAAT | 9873 |
rs571390495 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124436 | TAAAAAAAGAAGAGA[A/G]AGAATGGGGCAGAAA | 9873 |
rs571417047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140202 | TTCAGGAAAATACAT[C/G]TGTCAGAATATGTCT | 9873 |
rs571420558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060215 | CTCAGGAAAGTAACA[A/C]CCATTCAAGGAAGTT | 9873 |
rs571461946 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909800 | GCACCTCTGCCCGGC[C/T]GCCCCGTCTGAGAAG | 9873 |
rs571462996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091711 | CCACTTGGAATTTCC[C/T]CCCGTTATTTGGCCT | 9873 |
rs571465192 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981615 | GTGCTAAAAATCATC[C/T]TTAGTAAATGTGTTC | 9873 |
rs571472672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084583 | CTTCTTGTAGAGATG[G/T]AGTCTTGATATGTTT | 9873 |
rs571479975 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061071 | TCCCAGCAAGATCCT[C/T]GCAGAAGGCAGATGA | 9873 |
rs571493242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029712 | ACTTAAAGGGACAGC[A/G]TCCTTTTTCCCTGTC | 9873 |
rs571498872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029233 | GGAAAACAAAAGATA[C/T]GGAAACCACTTACAA | 9873 |
rs571516408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123255 | ATGTTGACTATCCAA[C/T]TGATAATTTTATACA | 9873 |
rs571519430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973647 | GGGAGATTTCCACTG[C/T]ACTGAGAGTGTTTCA | 9873 |
rs571530842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982246 | TTTGCCTGAAGGTCC[C/T]GAGAACTGTCCCATC | 9873 |
rs571536265 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075448 | GGTATTTGCTAGGAC[A/T]TTACTAGAACTAGAA | 9873 |
rs571539839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074854 | GAGTTCGAGGCTGTA[A/G]TGAACTAGGATCACG | 9873 |
rs571550090 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048778 | AGACAGGGATGTATG[-/TA]TATAGTTCACCTCAA | 9873 |
rs571550384 | in-del | -/TTTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850077 | TTTTTTTTTTTTTTT[-/TTTT]GAGATGGAATTTCGC | 9873 |
rs571553947 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845140 | AAAAGCTATGGAGAG[A/G]CTGAGTGAGGTGGCT | 9873 |
rs571556488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022978 | GTGATGCTAGAACAA[C/T]TGAATGACCATAAAC | 9873 |
rs571561446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022190 | GAGTGAATGCTTTTC[C/T]CTTAAGATAGAGATA | 9873 |
rs571576486 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092683 | TCAGTAGGTTAGCTC[A/C]TGAGACACACAGAAC | 9873 |
rs571576591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100321 | AGGCACTGACCTAAG[C/T]GCTTTACATGCTTTT | 9873 |
rs571579266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966465 | ACACCCGGACTAAAC[C/T]GAGCATATTACTTTG | 9873 |
rs571590529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944853 | TACAAGGGATGTGAA[A/G]GACCTCTTCAAGGAG | 9873 |
rs571599669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059520 | GGAATGCTCCCTACC[C/T]TTCACTCTAACTTCT | 9873 |
rs571608740 | in-del | -/GTAC | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035181 | TATGTATGTATGTAT[-/GTAC]GTATGTATGTATGTA | 9873 |
rs571619432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860352 | TTTTTAAGAACACAT[A/G]TAACAGTTACCAAGA | 9873 |
rs571621850 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865513 | TGATTTCTCTGGACA[C/G]GTCTCAAAAATACTC | 9873 |
rs571622135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859410 | GCTTGTGTTCAAGTA[A/G]CCCTTATTTTACTTA | 9873 |
rs571628838 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872157 | TTTTTGGCTTAGAGG[C/T]ACTCCAATTGGTAAA | 9873 |
rs571630857 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838278 | CTTTCTCAGTCTGGG[A/G]ACTAACCTTGGGGAG | 9873 |
rs571636690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093343 | TGAGAGTCCTGGCAA[A/G]TTATTGAATCTAAGG | 9873 |
rs571638384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913130 | CAAGAGAACAGCAAG[A/G]GGGAACTCCATCCCC | 9873 |
rs571642260 | in-del | -/AAAC | 0.0532157 | 0.154195 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855279 | AAAACTCCGTCTCAA[-/AAAC]AAACAAACAAACAAA | 9873 |
rs571650252 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934048 | TGGGAGGTTGAGGCT[A/C/G]CAGTGAGCCATGATC | 9873 |
rs571657898 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974684 | TACTTTCAGTATTCA[A/C]AAGTACCAGTGGTAA | 9873 |
rs571661940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867786 | TTTAAAAAATTTTGG[C/T]TATTATTAAGTTTGA | 9873 |
rs571666453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959008 | ATGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 9873 |
rs571669745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014511 | AAGACACCTTCCATG[A/G]TATCAGTAGGCCACT | 9873 |
rs571676003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868308 | AACAATGAGAACATA[C/T]GGACACATGAGTGGG | 9873 |
rs571696188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960784 | ATAATAAAGAACCCC[A/G]GGGTGTGAAATACAC | 9873 |
rs571698907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907594 | CTATTGAGATAATCA[C/T]GTGGGTTTTTTTTTT | 9873 |
rs571699933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952567 | TGACCTCAAGTGATC[C/T]ACCGGCCTCGGCCTC | 9873 |
rs571714234 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081928 | GCATTCAAGATCGGG[C/T]GCGGTGACTCACGCC | 9873 |
rs571716936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846371 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 9873 |
rs571751649 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082559 | CTACAAAATTAACTA[C/T]AATGAAATCAGAATT | 9873 |
rs571753112 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143121 | GGAAACGGCGGCACT[A/C]TACTGCAGGGCATTC | 9873 |
rs571760828 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045881 | ATGTAACTAACCTGC[A/C]CAATGTGCACATGTA | 9873 |
rs571766372 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048348 | TAGTCTAGTACTGGC[G/T]TGTTATTTACAGGTA | 9873 |
rs571778302 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847082 | GCTCACTGCAGCCTC[C/G]ATCTCCTGGGCTCCA | 9873 |
rs571783502 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052811 | ATAGCATGAAAAGAT[A/C]AGTTTCTACAGATAT | 9873 |
rs571786801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052240 | AATCTATGAAAAATT[A/G]TAAGTCAATAAACAT | 9873 |
rs571788739 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102129 | GTAACAGTGAAAAGA[A/T]GCTTAACATCACTAC | 9873 |
rs571790162 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852238 | CAGATGCTGGTGACG[C/T]TATGGAAAAAAGGGA | 9873 |
rs571795945 | snp | A/G | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140843 | GGGGCCCCAGGGTTC[A/G]AAGTTAACGGTCAGT | 9873 |
rs571799573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999463 | TAGCTGGAACTACAG[A/G]TGCACGCCACCACAC | 9873 |
rs571818291 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102523 | GAATGAATAAACAAA[C/T]TGCAGTTGTACTCTG | 9873 |
rs571822356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138814 | GGTTTTATCATGTTG[C/G]CCAGGCTGGTCTCGA | 9873 |
rs571824222 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079062 | GATAATAGTTTACAT[A/G]AGTGTGTTCACAAAA | 9873 |
rs571833639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993863 | GTATACATATGTAAC[A/T]AACCTGCACGTTGTG | 9873 |
rs571850676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094531 | CAATGGGATCATGGA[C/T]AAACAGTAACATATT | 9873 |
rs571851017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102792 | TTTGGACTTCCCAGC[C/G]TCCAGAACTATAAGC | 9873 |
rs571851553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900253 | TGACCCACACCCCAT[A/C]TACCTCAGCTATGGT | 9873 |
rs571853877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944040 | GGGAATCCTCCCTAA[C/T]TCATTTTATGAGGCC | 9873 |
rs571860733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991874 | GATGCCCTCTCTCAC[C/T]ACTCCTATTCAACAT | 9873 |
rs571862127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991267 | GATGGATTCACAGCC[A/G]AATTCTACCAGAGGT | 9873 |
rs571892018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847898 | GGGTTTCACCATGTT[C/G]GTTGGGCCAGTCTTG | 9873 |
rs571896257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986055 | AAGCCAGTGTGAAGA[A/G]GATAGGAAAAGCAGC | 9873 |
rs571896294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839459 | AAGAAGGCAACTTAG[A/G]AGACTTTTGTAATCC | 9873 |
rs571914629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095552 | AATAAAACTAGGAAA[C/T]ATATGTATGGACATA | 9873 |
rs571928916 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052995 | GGGATTACAGATGCC[C/T]GCCACCACACCTAGC | 9873 |
rs571938865 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891485 | CATTTTTGGGGTTAT[C/G]AGAAGTTTGGGAATG | 9873 |
rs571959634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840262 | AGAAGGCACTCAATA[C/T]ATATTTGCTGAATGA | 9873 |
rs571964629 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109332 | ATGGACATTTTAACA[A/G]TATTGATTCTCCCAA | 9873 |
rs571979419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892558 | TATCAAAGATCAATA[C/T]AAATCAGGATCTAGT | 9873 |
rs571984091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986499 | CAGGCGTGAGCCACC[A/G]TGCCCGGCCCCAATT | 9873 |
rs571989353 | snp | C/T | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140409 | CATTTCATGCACAAG[C/T]TCAATCCACGTCTAG | 9873 |
rs571990935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874635 | ACTACATTCTATTTT[C/T]TCAAAGCAGTTATTC | 9873 |
rs571995302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054427 | GTATTTCCTGTGATA[A/G]GGAATGATGGGCATG | 9873 |
rs572016828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879328 | ACTCAATAGTCTTTA[C/T]AAGAAGAAAATAGAA | 9873 |
rs572022112 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887304 | TTTGTTATATGTACT[-/G]CCTTCCACAGAGCAG | 9873 |
rs572025673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118275 | GGTGAGCCGAGACTG[C/T]GCCACTGCACTCCAG | 9873 |
rs572051889 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084882 | GAGTTTAAAGACTTT[A/G]CCGTTATGTGCCAGG | 9873 |
rs572055260 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837061 | TAAAGACAGAATACA[A/G]GACTGGGTGGCAAGA | 9873 |
rs572064960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945778 | GACATTTATGCAGCC[A/G]AACGATACATGAAAA | 9873 |
rs572090745 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901442 | AAGTAAAAATAAAAA[A/C]AAAAATTGCCAGTTG | 9873 |
rs572094376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909165 | CCTTGGCCTGCTGAG[G/T]GTCTGGGATTGCAGG | 9873 |
rs572099225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939006 | TGAGCTACTAAACAT[A/G]TAATGCAGGATATTT | 9873 |
rs572105193 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981988 | CCCTGTCTCAAAAAC[C/T]ATATATACTAAAACA | 9873 |
rs572126291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017702 | GTACGGTAGTTTTTC[A/C]CCTCTGCACCTTGTT | 9873 |
rs572131133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902222 | TGGAGGGGTACAACA[C/T]AAAAAATTTCAGGGA | 9873 |
rs572131776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886151 | CAGGGATTCCTTGTA[C/T]TGGGTCCCTGAAAGA | 9873 |
rs572138563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872380 | TACATGCAACCATCA[C/T]CACAGTCAAATTTAG | 9873 |
rs572142986 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131731 | AAATTAAAAAATTTA[A/C]AAAATAAGAACACCA | 9873 |
rs572143108 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123417 | AGCGCTCATCCTTAA[A/T]TACAAATGAGAATCA | 9873 |
rs572153041 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021031 | GCAGGTGCATGCCAC[C/T]GCGACCAGCTAAGTT | 9873 |
rs572153390 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951669 | TTACATTTATCTTTA[A/T]CAAACCTATAACTTA | 9873 |
rs572164226 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022534 | AATCCCACAAAATGT[C/T]TGCAGGATCTGTATG | 9873 |
rs572183490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018729 | AATTTTCATGTACTC[A/T]AATTTTTTAATAACT | 9873 |
rs572193296 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917682 | CTTGACGTCAGGAGT[C/T]CAAGACTAGCCTGGC | 9873 |
rs572211986 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002885 | TAATGTAATTGTTTA[C/T]TAACATCTGTCCCTC | 9873 |
rs572275441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886817 | TCCCAACCTCTCCCT[A/G]TCTAGAGCAGGGAGT | 9873 |
rs572280189 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939743 | TATGCCTCAGCCTCC[C/T]GAGCAGCTGGGATTA | 9873 |
rs572301410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025681 | TAGAATTTTAAAAAT[G/T]TTTTAAATCTCCTTG | 9873 |
rs572311350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931563 | CAAGGTCAGGAGTTC[A/C]AGACCAGCCTGGCCA | 9873 |
rs572338854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088235 | AGATATGTTTTGATA[C/T]ATAAATACCATCATG | 9873 |
rs572342014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880014 | CAAAAAAAAAAAAAA[A/G]AAAAAAAGTAATCCT | 9873 |
rs572347904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969493 | CTTAATTTTTTGAGG[G/T]TAGAGAGTATTTGTC | 9873 |
rs572348665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932377 | TCTACACTGTTCACT[A/G]GCTACTCATCACATT | 9873 |
rs572356421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915964 | AGCAAACTAATGTAG[A/G]AACAGAAAAGCAAAT | 9873 |
rs572370600 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043827 | GCTAGATGTAGAGGA[C/T]CCATTGAGGACTTGA | 9873 |
rs572376555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129578 | AACCCCAGATGGGAC[C/T]GTCCAGTTGCAGAAA | 9873 |
rs572400334 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973054 | TAAAACAATAAACAA[C/T]TAAAATTTCCATTAA | 9873 |
rs572401778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080195 | CCAGCCACTCAGTAG[C/G]CTGAGGCAGAAGGAT | 9873 |
rs572410425 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088024 | AGCTAGGACTACAGG[C/T]ACATGCCACCACATG | 9873 |
rs572417732 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911975 | TTCACATATAGAAAT[A/G]CTACTTATTTTTGTA | 9873 |
rs572422383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026710 | ACCCAAATCTCATCT[C/T]GAATTGTAATCCCCA | 9873 |
rs572439007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128958 | CTCACTGCAACCTCC[A/G]TCTCCCGGGTTCAAG | 9873 |
rs572443912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924317 | GAGTCTTGCTCTATT[A/G]CCCAGGCTGGAGTGC | 9873 |
rs572450378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896827 | TGGATTTTTGTTTTG[C/T]TTTGTTTTGTTTTGT | 9873 |
rs572467569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970350 | TTACAATTCTAATGT[A/G]TGAAAATTGTCTTTT | 9873 |
rs572477396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855600 | TACCATACACACGAA[C/G]AAACGTGAAAAGCAC | 9873 |
rs572480655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925004 | ATTACATTTTGGCAG[A/G]AAACCATTGGAGTAT | 9873 |
rs572489305 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122149 | CTTTAATACCAGAGT[G/T]TTTTGTTGTTGTTGC | 9873 |
rs572496946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875389 | TATTTATTTGACAGA[A/G]TCTCGCTCTGCTGCC | 9873 |
rs572499885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916437 | CCCACTTGGGCCTCC[C/T]GAGTAGTTGGGACAA | 9873 |
rs572501328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110868 | TGTTGGTATGTCATG[C/T]TTCCATTATCATTTG | 9873 |
rs572504169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962786 | CACACCAAAATGATA[C/T]CACAAAGGTCCCTCC | 9873 |
rs572519422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021529 | ACATGAACACATAGA[A/G]GAGAACAACAGACAC | 9873 |
rs572533645 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876106 | GGGAGGATTGCTGAG[A/C]CCAGGAATTCGAGGT | 9873 |
rs572538612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909983 | GGGAGGTGAGGAGCA[C/T]CTCTGCCCGGCCGCC | 9873 |
rs572544301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848801 | TTTTAGTTCTGGGAC[A/G]TTCAAGTAAATATAA | 9873 |
rs572546206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114565 | AGCCAGCACATCACA[A/G]AAGCTCACCCAAGAC | 9873 |
rs572559177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856885 | TTATATATACTTAGA[A/G]GACATTGCCTTCATA | 9873 |
rs572577020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910389 | TTGTCGAAAAGAAAA[A/G]GGGGAAATGTGGGGA | 9873 |
rs572581136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947447 | AAGTTGTCTGACTAG[A/C]ACTAAAGCCAAAGTC | 9873 |
rs572582477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022436 | ACAATACAACGTCAA[C/T]ATTCCAAAGTTAATT | 9873 |
rs572596770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063448 | TAACAATATTAACCT[C/T]AAATGTAAATGGGCT | 9873 |
rs572609940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125449 | GTGGCTCATGCCTAT[A/T]ATCCCAGCACTTTGG | 9873 |
rs572616365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995081 | GGAATCAAATAATAT[C/G]TGGCCTTATGTTTCT | 9873 |
rs572617267 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072794 | TTTTTAAGTTTCTAT[A/G]CAGATGAAATTCACC | 9873 |
rs572642286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014832 | CTTCCAAATTGACCT[A/C]AAAAAAGAAATCAAA | 9873 |
rs572643776 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966492 | TTTGTTATACTAATA[C/T]GGGAATTACAGCATT | 9873 |
rs572656288 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026388 | ACTGGGAGCAAAATG[A/G]CTGACTGAGACAATG | 9873 |
rs572669768 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021525 | GAACACATGAACACA[C/T]AGAGGAGAACAACAG | 9873 |
rs572700540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048286 | GTACCGACACACATA[C/T]GGGACCCAAAAGTTA | 9873 |
rs572705624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036508 | ACTGTAAAATGGGCA[C/T]AATAATGAAACCTAA | 9873 |
rs572725381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995603 | CAACTACTTGGGAGG[C/G]TGGGGTGGAAGGATC | 9873 |
rs572726848 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982660 | ATAAACAGGGAAATG[A/C]TAGATCAAGTTTGGG | 9873 |
rs572732884 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923891 | TTGCAGTAAGCCGAG[A/T]TTGTGCTATTGAAAT | 9873 |
rs572748689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051748 | AACAACAAAAAAAAT[A/T]TGAAATAAATAGTAG | 9873 |
rs572754660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907872 | TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC | 9873 |
rs572756181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104738 | CGCACCCGGCTAATT[C/T]TTGTATTTTTAGTAG | 9873 |
rs572760901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899671 | GAGCCCAGGAGGTTG[A/G]GGCGCAGTGAGCCGT | 9873 |
rs572771423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125489 | GAAGGGGGACTGCTT[G/T]AGCTCCACAGTTCAA | 9873 |
rs572772395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973175 | GAGTTCAAGACCAGC[C/T]TGACCAACATGGAGA | 9873 |
rs572794747 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983853 | AAATGTTTGCCGCAC[C/T]TAGGGAATAATATAA | 9873 |
rs572796897 | in-del | -/GTTGTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961429 | GTTGTTGTTGTTGTT[-/GTTGTT]TTTAATAGATGGGGT | 9873 |
rs572808524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919143 | AAAAATCTAAAAAGT[G/T]TCAAACTTCCCTTTA | 9873 |
rs572810117 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73052483 | TGTGAATTACTTAAA[A/G]GCTAATGCAGTGTAT | 9873 |
rs572815010 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974055 | ACCAGCAGAGTTGAT[A/T]ACAGACAGGTAAGGG | 9873 |
rs572816824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867330 | AGCCCTGGACTTGAA[A/G]TAAGGAGACTTAAGC | 9873 |
rs572819762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096904 | AAGAGTGTTAAATTA[C/T]GTGAAATGCTTTTTC | 9873 |
rs572836793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124713 | GTGAGCTGAGATTAC[A/G]CCACTGCACTCCAGC | 9873 |
rs572846375 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928453 | ACTTTCATGTTCCCA[A/C]ATAAGTTATTCTCTT | 9873 |
rs572850025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920226 | AAATAGACTGGCAAG[C/T]CTGGTCAAAATAAGA | 9873 |
rs572850276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927888 | CGCTCTACTTTAGAT[C/G]CAAGACAGGAATGAC | 9873 |
rs572850394 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968625 | TATCCATAAATGGGG[G/T]GTTATTCTGATTTCC | 9873 |
rs572870755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083920 | CAGTCAGAGGATCTA[C/T]ATTCAAACCCCAGCT | 9873 |
rs572900150 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132912 | CATATATGTTATAAA[A/G]AACTCTTAAAATTCA | 9873 |
rs572907596 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966353 | TTAGTAGAGACAGGG[C/T]TTCGTCATGTTGGCC | 9873 |
rs572910160 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094890 | CGAGGCAAGCGGAAC[A/G]AACAACTGAAGCTAT | 9873 |
rs572919145 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066851 | GATGCTGGAGAGGAT[A/G]TGGAGAAATAGGAAC | 9873 |
rs572927269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858808 | AAATATCAGGAAAAT[C/G]GATTTGTGCTTCCAG | 9873 |
rs572930774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044940 | CCGGGTGTGGTGACA[C/T]GTGCCTGTAATCCTG | 9873 |
rs572931672 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976928 | CTCAAACTATGAAAC[-/A]TTTTTTTTTTTTTTT | 9873 |
rs572936057 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863069 | CTAGGACCGCAGGAA[C/T]GTACCACAATGCCTG | 9873 |
rs572939568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965474 | GCTACTTCTATAAAG[C/G]CTTTTGTGACTTTCC | 9873 |
rs572942649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937287 | AAACAAAAAAATTCT[C/T]GGCATTTCAGTTTAG | 9873 |
rs572974790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965972 | TATAAACATCGGCAG[A/G]AAACATGATTCTATT | 9873 |
rs572978810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059800 | ATTCTCATCCCAAGA[A/C]AATGAAAACCCACGG | 9873 |
rs572979179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937781 | GGATAATTTCAATTA[C/T]ACAGGGTGCTAGAAG | 9873 |
rs572981968 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040031 | CAAAATGGAGGACTT[A/G]CGTTGAACACAATGT | 9873 |
rs572987103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72929845 | TTTTCCCAAAAGACC[C/T]TTAATTCCTTGAGAA | 9873 |
rs572994427 | in-del | -/ATT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864026 | CTTATCTCCAACATC[-/ATT]ATTAAGCATGGTTCT | 9873 |
rs572998014 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897063 | AATCTCCTGACCTCA[C/T]GATCCGCCCATCTCA | 9873 |
rs573000031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060496 | AGGAACACATTACAG[C/T]GAGAAAGTTTTCCAG | 9873 |
rs573010256 | snp | A/C | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141585 | GGCAGCATTGCCATG[A/C]GCGCGCACACACACA | 9873 |
rs573056708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998528 | CCTGGGTGACAGAGC[A/G]AGACTCTGTCTCAAA | 9873 |
rs573057789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067534 | TGAATAAAAAACAAT[C/T]TGAACTTCCCCTCTG | 9873 |
rs573068103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958293 | AAGGCTGAGGCAGGC[A/G]GATCACTTGAGGTCA | 9873 |
rs573092524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105260 | CACAATAATGTGCTA[C/T]AAAAGGTGGTGATAA | 9873 |
rs573092594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107211 | AGGCATGCGCCACCA[A/T]ACCCAGCTAAGTTTT | 9873 |
rs573098949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959140 | TCTGTATGATTCTGT[C/T]AATACTCTTTACCCA | 9873 |
rs573099296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076937 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 9873 |
rs573104242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999070 | TCTAATACCATCATT[G/T]GAACCCCTAGATCCA | 9873 |
rs573109802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943717 | GCACTCAGAATGATA[C/T]CTCACACTTAGTATT | 9873 |
rs573120099 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099608 | CATACAACCGAGTAT[C/T]ATCCAGTCACAAATG | 9873 |
rs573123412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067201 | GACATGGATGAAGCT[A/G]GAAACCATCATTCTC | 9873 |
rs573134037 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138101 | CAATAATACAAACTA[A/T]GCAACAGCAACAGGA | 9873 |
rs573137985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890829 | GCTATTAAACACAAA[A/G]CTATTTTAATTCTCT | 9873 |
rs573144638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844608 | GCTTTGCTTCCTAAC[A/T]GTCTTGCCTGTCATG | 9873 |
rs573160220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068582 | CTTTATATATTTTTG[G/T]TTTAAAGTTTTATCA | 9873 |
rs573183989 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064326 | CTAAATGCCCACAAA[A/C]GAAAGCAGGAAAGAT | 9873 |
rs573184962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141320 | CCTTAATTTGTTTTC[C/T]CTTGGGGTGGGGAGG | 9873 |
rs573186732 | in-del | -/AAAAT | 0.00478562 | 0.0486817 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080961 | CTCAAAAAAACAACA[-/AAAAT]AAAATAAAATAAAAT | 9873 |
rs573200937 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837839 | CCTGGCTGTCTGGGC[C/T]GGTCTGCTGGCTTGG | 9873 |
rs573201152 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922808 | ACCCAATATAAGTCA[A/C]CATTTTAATAATTTT | 9873 |
rs573217959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037666 | ATGTTATGAATGTGG[C/T]CATTTAATCATATAA | 9873 |
rs573219212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140490 | AAAGACATTAACCAC[C/G]AGGAGAGGTGAGCAG | 9873 |
rs573220087 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099942 | TAATGAGGCCTTTCC[A/C/T]GAGCTCTAAGTTTCC | 9873 |
rs573225008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069738 | TGAAGAAGCAATATT[C/T]ACAGAAATGACTAAA | 9873 |
rs573227726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093493 | GGTGTCAGAATTGAG[A/C]GCTGTCTTAGAAGAG | 9873 |
rs573233980 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115081 | GCAGTGGCAAGGCGT[A/G]CTGAAATTCAAGTTC | 9873 |
rs573247480 | snp | A/C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097960 | CTAGACTTGCATAGC[A/C/T]CATGGTGCCCAGCTC | 9873 |
rs573257117 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851618 | CATGGTGGCATGCGC[A/C]TGTAGTCCCAGCTAC | 9873 |
rs573261273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845287 | ATTGGTGGGTGTGGT[G/T]GCACGTGCCTGTAAT | 9873 |
rs573270284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047525 | AAAAATACTGGTCAT[C/T]GACAGTACCTAGCCA | 9873 |
rs573280940 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030589 | CCTTAACTTTGTAAA[C/G]ATGGTGGTGGTCAAT | 9873 |
rs573286658 | snp | A/T | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73142704 | GCGCGCTTTCCCGCC[A/T]GCTCGCCCCGGCGCG | 9873 |
rs573312840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031150 | ATTTGATCTGTTATA[C/T]ATGGAATCTAAAAAA | 9873 |
rs573318709 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036496 | TTAGTTTCCTCAACT[A/G]TAAAATGGGCATAAT | 9873 |
rs573333024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976442 | GACTACAAGCACGTG[C/T]TAATTTTTAAATTTT | 9873 |
rs573349448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992108 | TCACAAGCATTCTTA[C/T]ACACCAATAACAGAC | 9873 |
rs573358915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921518 | TCCCCCATGTGAGCA[G/T]AGTGCATTTAAACTC | 9873 |
rs573367558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922523 | CTTAAACATTTTGTA[A/G]CAGGGATCTTTGAAA | 9873 |
rs573422878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967857 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 9873 |
rs573439255 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859563 | ATGTATGTATAGGGA[A/C]AAACACAGTATACAT | 9873 |
rs573462914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73024704 | ACAGAGTAAACAGAC[A/G]CCCTACCGAATGGGA | 9873 |
rs573482746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968646 | TCTGATTTCCAAAAT[G/T]ATAGTGCTGGCATGG | 9873 |
rs573494410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081304 | AAGGGCATGGTGGCA[C/T]GCACCTGTAGTCCCA | 9873 |
rs573501174 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879597 | ATAGAACTTATAGAG[C/G]TAAAAATATAACATT | 9873 |
rs573518260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915201 | CACCATGAGATACCA[C/T]CTCACACCAATAAGA | 9873 |
rs573518433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008416 | ACAAGAAGAATGGTG[C/T]TTTAATAAATGTTCA | 9873 |
rs573532712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72947194 | TTCTTAGTTAAGGGC[C/T]TTAAACCAAGTGGAA | 9873 |
rs573541908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840483 | GGAGAATAAACGCTC[C/T]TTAAGGCCATGAAGT | 9873 |
rs573556982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072258 | AATAATGGGGATCAG[C/T]ATCAACAATGATTTC | 9873 |
rs573561114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081978 | GAGGCTGAGGTGGGC[A/G]GATCACCTAAGGTCA | 9873 |
rs573563616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096465 | CTGAGGCAGGAGAAT[C/T]ACCTGAACACAGGAG | 9873 |
rs573567289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132794 | ATGCCCCCTGCACTC[C/T]AGTCTGGGTGACAGA | 9873 |
rs573570967 | in-del | -/AAACAAAC | 0.0019972 | 0.0315375 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855287 | GTCTCAAAAACAAAC[-/AAACAAAC]AAACAAACAAACAAA | 9873 |
rs573586129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040900 | GCTCCCCCCCCTCTT[G/T]GGTAACTATCATTCT | 9873 |
rs573598395 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854749 | GAGTAGTCAAATTCA[C/T]AGAGACAGAAAGCAG | 9873 |
rs573617798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072900 | TTAAAAGAGTAAAAA[C/T]AGCAAAAAATTTTAG | 9873 |
rs573619373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016895 | GTACAGGGATTTGAA[C/T]TGAGAAGACCATTTT | 9873 |
rs573624409 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088502 | ACTAAAATAGTAATG[A/G]AAGTTTTCTCTGGGT | 9873 |
rs573644186 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935293 | CCCCTAAAGTAAGAA[C/T]TTTAAACAGTCCCCT | 9873 |
rs573653718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73096782 | TCCCCAGCCTAGACC[A/G]TGTCACTACACTCTG | 9873 |
rs573685994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955537 | AGTAGGTGGGTGGGG[A/T]GGAGCTAAAAGTTCC | 9873 |
rs573688174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041532 | TGTATATGTCTTTTT[G/T]TGAGAAATGTCTATT | 9873 |
rs573688949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994859 | GACATATAATTCACA[C/T]ACAACAAAATTCACC | 9873 |
rs573690027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964694 | CAGCCCCAGGTCTTT[A/G]TGGTAATAGCCTTAC | 9873 |
rs573707067 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931311 | GAGGTTTCACCATGT[C/T]GGTCAGGCTGGTCTC | 9873 |
rs573708461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849948 | AAAATGGTTGAAAGC[C/T]GGAAAAACACTTAAA | 9873 |
rs573717143 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088970 | GGAATAGCTTTTGTA[A/C]CCTTGATGTGCATAT | 9873 |
rs573722787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956336 | CCATCATAAAGGTGG[C/T]TGATTCAGGAGGGTT | 9873 |
rs573728481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925358 | TTCACTCAGCTTCTT[A/G]AATCCTACTTTAAAA | 9873 |
rs573745789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887992 | AGATGTCAAAACAGG[C/G]AAGAGATTATATGGA | 9873 |
rs573746448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872661 | TAACATTCTATTGTA[A/T]GGATATACATTAGAA | 9873 |
rs573747204 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892290 | TGTCTACTAAGACTT[A/G]GGAGTCCAATGATCA | 9873 |
rs573750280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995500 | TGAGCCCTGGAGTTC[A/G]AGACCACCCTGGGCA | 9873 |
rs573758154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980178 | CCACTTGCTAAGCAT[A/G]AAAGAGAAGGGGTAA | 9873 |
rs573758241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124663 | CAGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC | 9873 |
rs573771308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850408 | TTTGAGACGGAGTCT[C/T]GCTCTGTTGCCAGGC | 9873 |
rs573779321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105490 | CTTGGGAAGTGAAAA[G/T]GGAATAGAGAAGAAA | 9873 |
rs573780452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926225 | CAGTCCAGCAGACTA[A/G]AGTGGGGACTGGTGG | 9873 |
rs573784137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880295 | TTTGTATGGAACCAC[A/G]AAAGTCCCTGAATAG | 9873 |
rs573793051 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866690 | GAAAATAAAGCTTCA[A/G]TAGATTGTTTTTCCT | 9873 |
rs573819613 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853061 | CTTAGTACCTGGGTA[G/T]TGAAACAATTTGTAA | 9873 |
rs573874221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064581 | GAAGAATCAAACAGA[C/T]GCAATAAAAAATGAT | 9873 |
rs573874559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019956 | TTCTCCAAGCCCACA[A/G]CACTACTATCTAAAA | 9873 |
rs573878399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917857 | CATGCCATTGCACTC[C/T]AGCCTGGGTGACAGA | 9873 |
rs573883375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843016 | ACTGTGCAGGACAAA[C/T]GTGACCATATAAAGA | 9873 |
rs573913766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865265 | ATGAAGAGATACAAC[C/T]CCCTCTAAATAATTT | 9873 |
rs573947659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990025 | TATGACATACAGGCT[A/C]GACTTTCCCAGAAGC | 9873 |
rs573961890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065233 | AATGTAATCTATCAC[A/G]TAAACAGAATCAATC | 9873 |
rs573963414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881966 | CTAACACGGTGAAAC[C/T]CCATCTCTACTAAAA | 9873 |
rs573969667 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916820 | TATGTTTTCTTTCGT[C/T]ACTTGTGCTTTCAAC | 9873 |
rs573972316 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100235 | ACCATTCCTCTTCGC[A/G]TCCCTTCCTCCCTTC | 9873 |
rs573975765 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036795 | ACAAATATTGTGTTC[A/C/T]CTCATAATTTTTTCC | 9873 |
rs573979045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028076 | GAGGGGAAATGTGGG[C/G]TTGGAGCCCCCACAC | 9873 |
rs573985763 | snp | A/C | 0.000235544 | 0.0108497 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902504 | TAAGCACAAACACAA[A/C]TGAACAACACATGAA | 9873 |
rs573997646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882469 | GTTAGATAGATGGGA[G/T]AAGTTCTGGTGTTTG | 9873 |
rs574010385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910628 | TGCCTGAAGGCAGCA[A/T]GCTCGTTAAGAGTCA | 9873 |
rs574029546 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855141 | AGCCGGGTGTGGTGG[C/T]GCATGCCTATAACCC | 9873 |
rs574036838 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068829 | AAAAAAAAAAAAAAA[-/G]AAAGAAAAAGAAAAA | 9873 |
rs574037277 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088846 | TTGGATTTTTTTATA[C/T]TTCACAAAAGATAAA | 9873 |
rs574066565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004072 | CGAGATAGTGCCACT[A/G]CACTCCGGCCTGGGC | 9873 |
rs574092906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949225 | AGGCCCATGGCGGGC[A/G]GATCACCTGAGGTCA | 9873 |
rs574097778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905177 | TAATTTCTTCTGACG[A/G]TAATTATTGTCGGCT | 9873 |
rs574103004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949720 | CTACATTCAATTTTA[C/T]GGTTGATAATATTCC | 9873 |
rs574104573 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853033 | TTAGAAAAAATAACT[A/C/G]TTGGGTACTAGGCTT | 9873 |
rs574104692 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006544 | ACTGTGACTACCCCG[C/G]TTTGAGCCACCCTCA | 9873 |
rs574108431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861719 | TGGAGCAACTGAGGT[C/T]GGGAGTTCAAGACCA | 9873 |
rs574121111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897676 | GTTTAGACACCCAAA[A/C]CCATGTTTTCTCCAT | 9873 |
rs574134099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905652 | GTCCATGTGTTCTCA[C/T]TGTTCAACTCCCATC | 9873 |
rs574155598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889397 | GGTAAATTAATGTAT[C/T]GCTGATGGAGGGCTT | 9873 |
rs574177764 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850375 | GGCCTAGGACAGAGA[-/T]TTTTTTTTTATTTTA | 9873 |
rs574179220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108718 | GGACTACAGGCGCCC[A/G]CCACCGCGCCCGGCT | 9873 |
rs574194476 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001207 | TAACCTTTTGCTCAC[A/G]GGGCAGCACTGACAG | 9873 |
rs574223082 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060622 | TCATGCTTTGATGGA[C/T]TGTCCACTCATCCCA | 9873 |
rs574233006 | in-del | -/T | 0.191461 | 0.24305 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003489 | TAGGTCATAGAGTGA[-/T]TTTTTTTTTTTTTTT | 9873 |
rs574238748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999925 | CTTCCAACTCAAAAT[C/T]ACTGGCCAGTGATCA | 9873 |
rs574240837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109300 | TTGCATTGAATCTGT[A/G]GATTGCTATAGAAAC | 9873 |
rs574250747 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042238 | CTGAGATTATTTTTA[A/G]ACTCTGGTGAAAGAC | 9873 |
rs574283459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091930 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAGGAG | 9873 |
rs574291902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123379 | AACAATGCATATTAA[A/G]CGGTGGTAACTCCTG | 9873 |
rs574301584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992419 | AAAGACTAAAGTTCA[C/T]ATGGAACCAAAAAAG | 9873 |
rs574315182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042838 | ATTTGAGGCTTTCTT[G/T]ATTTCTTTTTCTGCT | 9873 |
rs574319820 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918391 | CTTTTTCTTACCGAA[C/T]TGCCCTGTCTAGGAC | 9873 |
rs574322320 | in-del | -/ACAG | 0.00269875 | 0.0366345 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139989 | CAAAGGTTCTTTGAA[-/ACAG]ACAAACAGAAGTCCT | 9873 |
rs574323643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934637 | CTGTGCTTGGCCATA[A/C]ATTTCTTAATCAATG | 9873 |
rs574329180 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993853 | ACATGGCACTGTATA[C/G]ATATGTAACTAACCT | 9873 |
rs574337361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015617 | ATGATCTATTTTATA[C/T]AGATTACAATCTATT | 9873 |
rs574342633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068251 | ATGCCATTATGTGCA[C/T]GTTCTCGCTTGTGAG | 9873 |
rs574355590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885471 | GTCTAGTTTGGCATA[C/T]TATGGAAATAATAGG | 9873 |
rs574361740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993675 | AAAAAACCAAACACC[A/G]CATGTTCTCACTCAT | 9873 |
rs574367772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016119 | ACCAGCTTGGCCAAC[A/G]TGGTGAAAATCTATC | 9873 |
rs574370270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112698 | CTGTCGCCCAGGCTG[A/G]AGTGCAGTGGCATGA | 9873 |
rs574370665 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839543 | AGAGAAGTGGAAAGA[-/T]TTGCGAGCTCTCTGC | 9873 |
rs574391775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886092 | CTCTGGAGTTCTAAG[A/G]GGGTGTTAGAAAACC | 9873 |
rs574395734 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109791 | AGATCTTAGAGGAAA[C/G]GCTTTCAGTCTTCCC | 9873 |
rs574431510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008357 | AAAGAAAAGAAAATG[C/T]GATTAAGTTCATAAC | 9873 |
rs574433509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889489 | AAAAAACACATATAA[C/T]GCTTGAGCAAAGGAG | 9873 |
rs574435761 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143584 | AATACCTCTTCCCCA[A/T]GCCCAGGGAGGTTTT | 9873 |
rs574448643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023919 | AAAGGTTACACACTG[C/T]ATTATTCCATTCATA | 9873 |
rs574469971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952393 | GCAGTGGCACTATTT[C/T]GGCTCACTGCAACTT | 9873 |
rs574482312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878682 | TGATAATATACTAAA[C/T]AGATAAAAATCTATA | 9873 |
rs574485988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901276 | GTGGTGCGTGCCTGT[A/G]GCCCCAGCTAATCGG | 9873 |
rs574490402 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093980 | CTTTGGAAGGCCGAG[C/T]CAGGCGGACAACTTG | 9873 |
rs574497396 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881157 | TATACGGAATATACA[C/T]GGAACTCAAACAACT | 9873 |
rs574497491 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908166 | GTTTATTTCACTTAA[C/T]ATAATGACCTCCAGT | 9873 |
rs574497907 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916624 | CCAGCCTCCTTTGTT[C/T]ACTTTTATATTGGGT | 9873 |
rs574519084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879150 | AAAAAAAAAGATATT[A/G]CAACTCTATCCAGCC | 9873 |
rs574520294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009092 | AAAGTCTAATGCAAA[C/T]TGAGGTTTTAATGAC | 9873 |
rs574522559 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101187 | GAAGGAGAAACATGA[A/C]ATTTATTCATAAAAA | 9873 |
rs574522832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893222 | GGCCAGGCTGGTCTC[A/G]AACTCCTGTCCTCAA | 9873 |
rs574525593 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025009 | GAAGTTGGCAAGGTC[A/G]TGGAGAAAAAGAACG | 9873 |
rs574537110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846324 | TAGCTGGGATTACAG[C/G]TGCACACCACCATGC | 9873 |
rs574540233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061300 | TTGTCGCATGGTTTT[C/T]GCAAACTGCAGACCA | 9873 |
rs574540338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908697 | CATTATTTTTTGAGA[C/G]AGAGTCTCACCCAGG | 9873 |
rs574549620 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838544 | GGCTGCCCCCCTCTT[G/T]GCTCCTAGGGTCCGC | 9873 |
rs574555233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902167 | AGCGTGAGCCACAGC[A/G]CACGGCCTACTCTGG | 9873 |
rs574555742 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73102041 | TTGAAGGCCATCAGG[C/T]TGAAGACCATATTTT | 9873 |
rs574557158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045055 | AGCCTGGGCGACAGA[A/G]CAAGACTCCATCTCA | 9873 |
rs574562461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028052 | GAGAACCTCTTCTAG[A/G]GCACTACAGAGGGGA | 9873 |
rs574580306 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963334 | CATTTACTACGCACT[A/G]TCTCATTTAGATTTC | 9873 |
rs574580536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915544 | AATGTGGTACATGGT[C/T]GGGCGTGGTGGCTCA | 9873 |
rs574586863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025560 | GGCTTAATACCTGGG[C/T]GATGCAATAATCTGT | 9873 |
rs574604113 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053427 | ATCACTTGCTTCACC[C/T]TGGAAAAAAGTTAGA | 9873 |
rs574619151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094518 | TCCAGTTGTCCATCA[A/G]TGGGATCATGGATAA | 9873 |
rs574621249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915903 | AAAAAAGAATGAGAT[C/T]GTGTCCTTTGCAGGA | 9873 |
rs574628252 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057688 | CCAGTTTATTCATCA[C/T]CAACAAAACCCTTAT | 9873 |
rs574636731 | in-del | -/A | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143775 | CATGACCAGAAATTG[-/A]AAAGGTGGAACTTCA | 9873 |
rs574639068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893886 | TGATATATTAGTCTT[C/T]AAGTCATCTTAACTA | 9873 |
rs574642742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839338 | CTGTGCTTTATTCTG[C/T]AGGCAAAAGAGGAGT | 9873 |
rs574646457 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945213 | GAGATATAGACCAAT[A/G]GAACAGAACAGAGCC | 9873 |
rs574651100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039210 | GGATTCCTCATAAAC[C/T]TACCTCCATAACAGA | 9873 |
rs574680163 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046545 | TTACTATAAATTATT[C/G]GTAGAAATATAAATT | 9873 |
rs574685759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985792 | TCTAACAATAGGTAG[C/T]ACAAACATGTTGATT | 9873 |
rs574705317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909527 | GGAGCCCCTCTGCCC[A/G]GCCGCCCTGTCTGGG | 9873 |
rs574716034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931449 | AATTTTAAAAATTAA[C/T]TTAAAAAATAATTTC | 9873 |
rs574717403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018548 | TAATCATTATATCCC[C/T]GGCTATAGCAGATCA | 9873 |
rs574719295 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119621 | CTGGCTAATTTTTTT[A/C/T]ATTTTTTTGTAGAGA | 9873 |
rs574731624 | snp | A/C | 0.030665 | 0.119967 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045591 | TACTATGCAGCCATA[A/C]AAAATGATGAGTTCA | 9873 |
rs574733763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945677 | CTAATATCTAGAATC[C/T]ACAATGAACTCAAAC | 9873 |
rs574734100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938019 | GTCTCTAAGGAGTAT[A/G]TCTAAGAAGTATGAC | 9873 |
rs574743441 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909902 | TCTGGGAAGTGAGGA[C/G]CACCTCTGCCCGGCT | 9873 |
rs574746607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119138 | GAGATCCTGTCTCTA[C/T]ATAAAATACAAAAAT | 9873 |
rs574747344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039966 | ATACCAAAGATGATA[C/T]GGAAATACATAGTTG | 9873 |
rs574755611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986464 | TCCACCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 9873 |
rs574759419 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72955490 | CACCACTGGCTAATG[C/G]TGATCAAGTCACCCT | 9873 |
rs574763137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870507 | CTGCCATTCAATGAT[A/G]TTGAGTTATAAACTA | 9873 |
rs574779987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127321 | GTTAAAACAAAGCAC[A/G]ATCAAGGAATATTGA | 9873 |
rs574787373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950731 | ATTTTTCATTTATAA[A/G]AATACTTAACTCCCA | 9873 |
rs574799201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056201 | GCGTCTTGTTAGTTT[C/T]ATCAGGACATGTCTT | 9873 |
rs574845460 | in-del | -/GG | 0.00676609 | 0.0577691 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73114846 | TCTCAAGCGGAAGGA[-/GG]GGGGGTCTTTTTTGA | 9873 |
rs574857509 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070720 | CGTGAGCCACCATAC[A/C]CGGCCTAAATGTCAA | 9873 |
rs574868104 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035201 | GTATGTATGTATGTA[C/T]GTACGTACTAAGACA | 9873 |
rs574871653 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862761 | GCAAAGGACCTAGAA[A/C/T]ACCCAAAACAACTTT | 9873 |
rs574872788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984372 | TAAAAATTATTCATC[A/C]CTACTAAGGAATGAA | 9873 |
rs574883792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73087417 | TACTGAAGAAAGAAA[A/T]GTTTTTGGGCCAGGT | 9873 |
rs574886901 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142661 | CTGCCCTCCCTCCCC[A/C]ACGCTGGGAGCCAGC | 9873 |
rs574896162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932287 | GTTGCCCTGCATCCA[A/G]CTCTCCCTCTCACCA | 9873 |
rs574916787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062635 | AGCACGAGAACTTCA[C/T]GAAGCATACACCGTT | 9873 |
rs574922301 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949171 | AAAAGAAACCTGGCC[A/G]GGCGTGGTGGCTCAC | 9873 |
rs574930318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035783 | TGGAGTACAGTGGCG[C/T]GATCTTGGCTCACTG | 9873 |
rs574930360 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028187 | TGTACCTGGAAAAGC[C/T]GCAGGCACTCAATGG | 9873 |
rs574944851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079048 | TATACCTTAATCTGG[A/G]TAATAGTTTACATGA | 9873 |
rs574953197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135253 | AAACACAGATACAGG[G/T]GAGAGTACAGTAGTA | 9873 |
rs574961579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953909 | GTGGAATAGTAAAAG[C/G]CCAATATGATTAAAT | 9873 |
rs574962366 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848270 | CCTTTATGCACAGCC[C/G]CTCTGTTCTCCCACT | 9873 |
rs574969304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882260 | AGCTTGGCCAACATG[A/G]TAAAACCCTGTCTTT | 9873 |
rs574982688 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091132 | AATGTTCCATTCTAT[A/G]AGTATACCACAATTT | 9873 |
rs574984428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903302 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAT | 9873 |
rs574991279 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065778 | AGATAATAAAATACC[G/T]AGGAATCCAACTTAC | 9873 |
rs575023805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919125 | ATAATAATATAAAAT[A/T]AAAAAAATCTAAAAA | 9873 |
rs575035243 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126245 | CTTGGGAGGCTGAGG[C/T]AGGAGAATCGCTTGA | 9873 |
rs575046982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946456 | TGTTAAATGATGAGT[C/T]ACTGGGTGCAGCACA | 9873 |
rs575063849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010643 | ATCTGTACGATTTCT[C/T]TGGCTATGAACAGTG | 9873 |
rs575073502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895269 | AATATACCCATTAAG[C/G]CTGGGGTGAAGAAAT | 9873 |
rs575075919 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123423 | CATCCTTAATTACAA[A/G]TGAGAATCATATGCT | 9873 |
rs575078748 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961906 | GATGTGTAAATGCCA[C/G/T]ATTTCGTAACAAGAA | 9873 |
rs575098660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855475 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAGAGTT | 9873 |
rs575106397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110209 | GCTGGCCTCACAGAA[A/T]GAGTTTAGGAATATT | 9873 |
rs575114490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962675 | AATGTGATTTCCTAT[C/G]AAATTCTGGAAAAGA | 9873 |
rs575115143 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912618 | GTCTGATTTTGGTAT[A/C]AGGGTAATGCTGGCC | 9873 |
rs575124541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002509 | AAGCAGTCCCAACAA[C/T]TGATTTTCTTGAAGA | 9873 |
rs575124792 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889680 | TTCACACCACTGCCC[G/T]TCAACCTGGGTGACA | 9873 |
rs575132365 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72963828 | CCTCGGCTCACCTCC[C/T]GCTGTGCGGCCTGGT | 9873 |
rs575151546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058810 | TGACCTCAGGTGATC[C/T]GCCTGCCTCAGCATC | 9873 |
rs575155020 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006073 | CACTGCATGTGGCTA[-/T]TTTTTTTTTTTAAAT | 9873 |
rs575160106 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856046 | TACAAAAGCACCAAT[A/G]TTTACACATTTAAGG | 9873 |
rs575170202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110826 | TGAACTTCCCACTTC[A/G]TACTGCTGTCGTTGT | 9873 |
rs575172105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002019 | TTTATTTTTTAAAAT[A/G]AGTCCTTAAAGTGAA | 9873 |
rs575185008 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059641 | AAAATTCAAGTTTTA[C/T]GTATCCTGGTACCAA | 9873 |
rs575198579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927313 | TACTACAATGGTGGA[C/T]ACATATCATTATACA | 9873 |
rs575214556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051738 | AGACATTCAAAACAA[A/C]AAAAAAAATTTGAAA | 9873 |
rs575222386 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093985 | GAAGGCCGAGTCAGG[C/T]GGACAACTTGAGGTC | 9873 |
rs575240365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927805 | GCCTACCATCCTGAA[C/T]AGGGTCAAGAGCACC | 9873 |
rs575281329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943612 | GAAGTGAGAATTCCC[C/T]GGGTCAGTCTATTTG | 9873 |
rs575308818 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051961 | CCACCAAAGATGTTT[A/G]CTTGGAAATATTCAG | 9873 |
rs575320038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72936741 | CTTCAGTTATTGTAT[G/T]TTTAACTCCAGAATT | 9873 |
rs575335420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866250 | GATGGAGCAACTCTG[C/T]TCTGTTTTTTGTTTT | 9873 |
rs575337035 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074922 | GTCCCAAGGATGGAC[A/G]GACAGACAGTGGGGA | 9873 |
rs575363270 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993874 | TAACTAACCTGCACG[A/T]TGTGCACATGTACCC | 9873 |
rs575372641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022321 | AAAGGAAGAAATAAA[A/G]CTATCTTTATTCATA | 9873 |
rs575375751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083058 | AATGAGAACTAAATG[C/T]GTGATGAAAAATTAA | 9873 |
rs575381751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971911 | CAAAGGAACGAGAGA[G/T]AAAAGTTTGGGAGGA | 9873 |
rs575387478 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066231 | TTGACAAACCTGACA[A/C]AAACAAGCAATGGGG | 9873 |
rs575387943 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993885 | CACGTTGTGCACATG[C/T]ACCCTAAAACTTAAA | 9873 |
rs575405114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937132 | AACACAATTATATAG[C/G]TGGAGGAAGACAGAG | 9873 |
rs575419409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972914 | AATAAAAGGATTGTA[A/G]GCTGGCACTCTTTTG | 9873 |
rs575430585 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957346 | GTTTCATCCATGTCC[C/T]TATAAAGGACATGAA | 9873 |
rs575472834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958176 | AAGATGGCTTGCTTT[A/G]AATCAAGTCAGAGGA | 9873 |
rs575486566 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948593 | ATTATCAATAATAGA[-/AT]ATGAGTGTATTAACA | 9873 |
rs575487368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924122 | TTTACTTTTTTAAAA[A/G]AAGTGATAAGGTCTT | 9873 |
rs575493204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085599 | GAGAAATTGAAAAGT[A/C]ACCACACAAACCCAC | 9873 |
rs575505875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965385 | CACTAAAACACAGTA[A/G]GAAACAATACACAGT | 9873 |
rs575510812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950838 | CCAAATGTTATCCCT[C/T]TCTTCCTGGGCACAT | 9873 |
rs575522547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858713 | TGTACAACCCCCCCA[A/T]GACACAAGTTTACCT | 9873 |
rs575524326 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137256 | GTAATACGGTATCCT[A/G]TTTACAACTCTATGG | 9873 |
rs575527401 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899587 | AAAATAAAAATAAAA[A/T]AAAACAAAATAAAAT | 9873 |
rs575533966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898777 | CTCTGTCACCCAGGA[C/T]GGAATGCAGTGGTGT | 9873 |
rs575534322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73126597 | TAGCATCAACTAATA[C/T]GAACTTTTATAATAT | 9873 |
rs575534429 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868839 | CCACATGCAGACATA[-/T]TTTTGCACAACTGTA | 9873 |
rs575537624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966937 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 9873 |
rs575537716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976343 | GTCACCCAGGCTGGA[C/G]TGCTGTGGCAGGATC | 9873 |
rs575549555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125659 | GCAGTGAGCCATGAC[C/T]GCACCACTATAACCT | 9873 |
rs575551347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844507 | CAGCAGCAATCCACC[A/G]GCATCAGCCACCCAC | 9873 |
rs575582594 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130906 | TATTTAAGTGTAGCC[C/T]TACTTGATCTTTTTT | 9873 |
rs575585093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843935 | ATCGCTTGAGCCTGG[C/G]AGGTTGAGGCTGCAG | 9873 |
rs575609504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055095 | GCAAGAGAATGAGTG[C/G]CAGGAGGGAAAATGC | 9873 |
rs575614788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133908 | GGCTGGAGAGGGTTA[C/T]GGGGAGCGACTGCTA | 9873 |
rs575615047 | in-del | -/AGACT | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926219 | GACTGCCAGTCCAGC[-/AGACT]AGAGTGGGGACTGGT | 9873 |
rs575616958 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836932 | GTTTTCACAACTTTG[C/T]TTTTTAAAATAAAAT | 9873 |
rs575635717 | in-del | -/ATAAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050838 | TCTACTCTAAGAAAA[-/ATAAT]ATAAGACTCAGAACA | 9873 |
rs575648714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990862 | ATAACTAAGACCAGA[A/C]CAGAACTGAACGAAA | 9873 |
rs575651421 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115612 | ACACGAGAGAGAAGG[C/G]AGATAGCTAGACACA | 9873 |
rs575657192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006233 | TTTTTAATTCCTGCC[C/T]AGACACCTTCCCTAA | 9873 |
rs575677214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946317 | AACCAAACACCACAT[A/G]TTCTCACTCATAGGT | 9873 |
rs575680488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991462 | GATGCAAAAATCCTC[A/C]ATAAAATACTGGCAA | 9873 |
rs575695550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840334 | AGCTAATAGGGGTCA[A/G]GGAAAATAAAATTGC | 9873 |
rs575697957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72851903 | TTTTTTTGAGATAGG[G/T]TCTTGCTCTGTTATC | 9873 |
rs575703037 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036799 | ATATTGTGTTCACTC[A/G]TAATTTTTTCCTCAA | 9873 |
rs575709880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095650 | CAAAACTCAAAGCGG[A/G]AGTACCTTTGTACAA | 9873 |
rs575716506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998467 | GGATCACCTGAGCCC[A/C]AGAGGCAGAGGTTGC | 9873 |
rs575731166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983566 | TAAGAGATACACTAT[A/G]AAAATATATTTTTAA | 9873 |
rs575758887 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928867 | CCTAATGCTATCCCT[C/T]CCCCCGTCCCCCACC | 9873 |
rs575773036 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72890673 | AGTGCTTCATATAAC[C/T]TTTTTTTTTTTTAAC | 9873 |
rs575782584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988134 | CTTACTGGTCTGTTT[C/G]TACAGGTGTTCAAAG | 9873 |
rs575811555 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891713 | CTTAGTTTGAATCCA[C/T]TGTATGCCATTTTAT | 9873 |
rs575813937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119099 | TCAAGCTTGGGAGTT[C/T]GGGGCTATCCTGGGC | 9873 |
rs575833800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088378 | TGTACTCCATGATGT[C/T]CACACAATGACGAAA | 9873 |
rs575834303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73141378 | CGCCCCGTGGGAAAA[G/T]CAGGCCAAACCCTAA | 9873 |
rs575845630 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72985469 | CCATACAACTTCATA[C/T]ACTTTAGTTCCTGCA | 9873 |
rs575845861 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026267 | ACAGGCATAAGCCAC[C/T]GTACCCAGCCTATAC | 9873 |
rs575853666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075916 | TTGAGTCCAGGAGTT[C/T]GAGACCAGCCTGGGC | 9873 |
rs575883281 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949187 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 9873 |
rs575895017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884133 | GACAACTTGATATTA[A/T]GATTCTTTATGTGAT | 9873 |
rs575895018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140593 | TGCCTGAATCGACTA[C/G]ATAAATTACTCCATA | 9873 |
rs575900591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72979187 | AAAGCAGTGTGAAAA[C/T]GAACTAATACAACAG | 9873 |
rs575908483 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023040 | ACCTCACGAGTTACA[C/T]AAAAATTGGCTCAAA | 9873 |
rs575914492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067668 | ACAAGTGCAAAATCA[C/T]CAGACAGAGAAGGAT | 9873 |
rs575920168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922384 | GTATATGTATATTTA[A/C]TGAACAGCAGTGACA | 9873 |
rs575937539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970496 | AAAAATCAAAGCTAC[G/T]TTAGTGGCATTTTAG | 9873 |
rs575941234 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847413 | ATTTACTAATGACCT[A/G]CTACGTGCTGGGCAT | 9873 |
rs575941740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980128 | GAAGCTGTCTTCCAA[A/C]GGTTTCTATCGTCTC | 9873 |
rs575949132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857223 | AAAGCATGTCATCTC[A/G]GAATAATTTCTTCCT | 9873 |
rs575992720 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847988 | TGAGCCACCATTCCC[A/C/G]GCCAACTCTAACCAT | 9873 |
rs575993117 | snp | C/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841159 | GGTGACAGAATAATA[C/T]CCTTTGTCCAGAAAA | 9873 |
rs576002545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73110693 | GATCTTTATTATTTC[C/T]TTTATTCTACTAATT | 9873 |
rs576003551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023351 | AACAGTAAGAAAAAA[A/G]TCAACACATTTTTAA | 9873 |
rs576020584 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73085221 | AAACGAAGACTAAGA[-/T]TTTTTTTTTAAATGT | 9873 |
rs576022177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971153 | TGTCATGCAGAGTAA[C/T]ACTATAAGTAACTGG | 9873 |
rs576040979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939900 | TGGGATTACAGGCAT[A/G]AGCCACCATGCCTGG | 9873 |
rs576063958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104004 | TACTAATACAAAAAT[A/G]CAAATAAATGTTTTC | 9873 |
rs576065710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040246 | CCAACCAACCCAGCT[A/C]TTTTCCCAGGAACAG | 9873 |
rs576110390 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883052 | TGCAAAGGTAATGGG[-/A]AAAGCATACTCTTTA | 9873 |
rs576112122 | in-del | -/AAAAG | 0.0111196 | 0.0737302 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949483 | AAAAGAAAGGAAAGA[-/AAAAG]AAAAGAAAAGAAAAG | 9873 |
rs576128246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932439 | ACCACATTATCTGAA[C/T]TTGGCATACCTCTTC | 9873 |
rs576163823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893674 | TTAGCTAGGCGTGGT[A/G]GCGCCGGAGGTTGCA | 9873 |
rs576166566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895059 | GAAGAGGAGTGGAAC[A/G]GTGCCTCTTAAGAGA | 9873 |
rs576174262 | in-del | -/GG | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879973 | ATCGCATTCCAGCCT[-/GG]GGGCAACAAGAGTGA | 9873 |
rs576174859 | snp | C/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138465 | CACGGGATCTTCACT[C/T]ACACACTAATTCTGC | 9873 |
rs576174911 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002438 | GCTCTCCATGGCCTC[A/C]CTGCATGACAACCAA | 9873 |
rs576193202 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909047 | TTTTTCCACCTCTCC[C/G]TTCCCCTCCCCCCTC | 9873 |
rs576224675 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080314 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAGAAAGA | 9873 |
rs576235341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137866 | AAGCCAGGAAAGGAA[G/T]CTTGCAGCTGGGTTG | 9873 |
rs576237610 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003967 | CAAAAATTAGCCAGG[C/T]GTTGTGGCTGGCACC | 9873 |
rs576251762 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887005 | CCAAATCTTCCCTAT[A/T]CTTAAAAGCCCAGCT | 9873 |
rs576253426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895905 | TATGAGACAACGCTA[C/T]ATGCAATACAAAATT | 9873 |
rs576253610 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118723 | TACTATAATGATGAT[A/G]GCAAACACTAACTGA | 9873 |
rs576289180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925989 | TCCTGGGGGAGGGCC[A/G]GGAAGGGCCCCCTGC | 9873 |
rs576289344 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071473 | GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATTG | 9873 |
rs576292668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72888811 | TTTTTTGTAGACACC[A/G]GGTTTTTTGCCATGT | 9873 |
rs576296226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872501 | ACTTTCTGTCTATAA[A/C]GATTTGCCTATTCCA | 9873 |
rs576316160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018865 | TGGGTATTCCAAAGC[A/T]GTTTTTAAAAATAAT | 9873 |
rs576326599 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053486 | CTTTTAAATCTAAAT[C/G]TCTTCAGTTCACAGC | 9873 |
rs576342445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033622 | AAGCATATCCACACT[A/C]CCAAACCAGGATAAA | 9873 |
rs576346878 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994204 | TTCCCTACTGGCAAA[C/T]TGTGTTTCCTGTACT | 9873 |
rs576354205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962950 | CTGGAGCCAGACTGG[C/T]TGAGTTCAAACTCCA | 9873 |
rs576374900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910047 | CACCCCGTCTGGGAA[G/T]TGAGGAGCACCTCTG | 9873 |
rs576376412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889306 | AGGGATGAAAACTTA[C/T]ATTAATTCAACATAT | 9873 |
rs576379602 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072234 | AGAAACAGAAGGTTT[G/T]GGGAGGAAAATAATG | 9873 |
rs576404050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019605 | ATAGACAAACAATGA[G/T]ATCTTTAGATGAAAG | 9873 |
rs576405474 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954887 | ACATATACACACACA[C/T]ACACAGATATATACA | 9873 |
rs576427059 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72975013 | GTTATATACGCCTAC[A/T]TATGAATGAGGAAGA | 9873 |
rs576436877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72916489 | GGCTAATTTAAAAAA[A/T]TTTTTTGTAGAGATA | 9873 |
rs576447405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014863 | TTCTTTTTTTTTTTG[A/G]GCTGGAGTCTCACTC | 9873 |
rs576447410 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72868908 | TTACCTTTTTTTTTT[A/T]AATTTTTTATTTTTT | 9873 |
rs576448096 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026850 | TTTGGCACTTCCCCC[C/T]TTGCTCGCTCTCTCT | 9873 |
rs576460160 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055007 | TGGACTGTGGTTCCA[C/T]GTGGCTGGGGAGGCC | 9873 |
rs576464772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011605 | CTTAGTTCTCAGAGC[A/G]TGTGTGGGACCCAGC | 9873 |
rs576473191 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847427 | TACTACGTGCTGGGC[A/G]TTGTCCTAGGGGCTG | 9873 |
rs576473215 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885974 | GCCTGTTCTGATTCA[G/T]ATCACTTCCATGGGG | 9873 |
rs576498751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129500 | AACTGCACATGCAAG[A/G]GATCTAGGTTGCATG | 9873 |
rs576506958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012707 | GTCATTGTATAATTC[G/T]TCATCTCTCTCCCCC | 9873 |
rs576509146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104819 | TGATCCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 9873 |
rs576523348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956167 | AGAGTAACAAATTTC[A/G]ATCCATTGAATAAAA | 9873 |
rs576524214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917078 | CAACCTCCACCTTTC[A/G]GGTTCAAGCGATTCT | 9873 |
rs576536572 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863794 | ATTTACAACATCACA[A/C]CTATTAGAATGTCTA | 9873 |
rs576536593 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72845208 | GGTGGATCACTTGAG[C/G]CCAGCAGTTTGAGAC | 9873 |
rs576543509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048426 | CTGTGTATGGACCAG[C/T]TATTGCTGAATCAAT | 9873 |
rs576556843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72896951 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 9873 |
rs576559024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860718 | GGCGTGGTGGTGCTG[A/G]GAGGCTGAGGCATAA | 9873 |
rs576559561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910461 | TAGACATAGGAGACT[C/G]CATTTTGTTCTGTAA | 9873 |
rs576568698 | snp | C/T | 8.23771e-05 | 0.0064173 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72849829 | TGGAACTGCTGTCAT[C/T]GAAAACATCCATGTT | 9873 |
rs576571316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007382 | TCCCAGCATTTTGGG[A/T]GGCTGAGGCAGAAGG | 9873 |
rs576578276 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901491 | TAGATTAATGATGTC[A/G]GGGGCTGAGGTGAGG | 9873 |
rs576579319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128902 | TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCCAGG | 9873 |
rs576579386 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841815 | ACTGATTTTAGTTTA[A/T]CTTAAACAGTTATCA | 9873 |
rs576582329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113676 | GCTTGTTTGTACCCG[C/T]CCTTCTTGGGAAAGT | 9873 |
rs576584432 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046464 | ATTAGATATCATTTT[C/T]GGCCCAGGATGGCAA | 9873 |
rs576586250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011442 | CCAGCAGCACTTACA[A/C]TGCTAACCTAACAGT | 9873 |
rs576590259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73105429 | CTACCAGGCTCTTTA[A/T]TTGGTAACATTACTT | 9873 |
rs576598640 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958214 | TGGAGCTAAGGACTA[C/G]AGTGCAAAAGTGACA | 9873 |
rs576622316 | snp | C/T | 5.63037e-05 | 0.00530553 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842886 | AAGATAATTAACAGC[C/T]GGTTGCTTTTGCAAC | 9873 |
rs576623240 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049276 | TAGTAAAACTTTAAG[A/G]AAAAAATTAAAACAT | 9873 |
rs576625989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897591 | CCATGGAAACCAAGG[A/G]ACAACTGTTGTCATT | 9873 |
rs576632519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008236 | CCCAGCTACTCAGGA[C/G]GCTGAGGCACAAGAA | 9873 |
rs576649525 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73044139 | ACATCCAAGGCCTGC[C/T]ACTATATGTCACCTT | 9873 |
rs576649832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120294 | TTATAATGTAGCATA[C/T]GGTCTTTATGTAAAC | 9873 |
rs576651463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097924 | AGCGATCCTCCTGCC[C/T]CGGCCTCCAACTGGC | 9873 |
rs576660667 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954426 | GCCCAGGATGATCAC[-/A]AACTCCTGGGCTCAA | 9873 |
rs576662910 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72992443 | AAAAAAGAGCCCGCA[C/T]TGCCAAGTCAATCCT | 9873 |
rs576665379 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73074326 | AGAATAAAACTCTGT[A/G]TGTGCAAGGACTTAT | 9873 |
rs576687650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901148 | CGTAATGCCAGCACT[G/T]TGGGAGACTAAAGTG | 9873 |
rs576688613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057801 | CCACAGCTATACAGG[A/G]AATGAGTTCCCCTCA | 9873 |
rs576690046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135391 | CACCTGACTAAAATT[C/T]AATAATTTTTCCATA | 9873 |
rs576696627 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962507 | TCACTGTAAAAAGAA[A/C]AGGAGTTTACAAAAT | 9873 |
rs576702377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098578 | TGTTTACAGTATGGT[C/T]AGTTGGAATAGAATT | 9873 |
rs576716654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030205 | CTATGTATATGTATG[C/T]GTGTGTGGGTAATCA | 9873 |
rs576717520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989130 | ACAATCATTATGATT[A/T]TAGTTTTCAGGCTTA | 9873 |
rs576724440 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72988932 | AACATTTATTTGCAT[A/C]ATAATTTTCTCAGAA | 9873 |
rs576725696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022453 | TTCCAAAGTTAATTG[C/T]TCTCCTACATACATG | 9873 |
rs576734182 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027150 | GAGGGCTCAGAAGAA[C/G]AGAGGAGGATGTCGG | 9873 |
rs576750981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075875 | TGTAATCCCATCACA[A/G]TGGGAGGCCAACGCA | 9873 |
rs576759862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949160 | TTATCACCACAAAAA[A/G]AAACCTGGCCGGGCG | 9873 |
rs576772842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966199 | TGGTCTCACTCTGTC[A/G]CCCAGGAAGGAGTGC | 9873 |
rs576777702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893153 | ACAGGGCATGTACCA[C/T]CATGCCCAGTTAACT | 9873 |
rs576794416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942019 | GTAACATGTAAAGGC[A/G]GTGATACAGTTTGAA | 9873 |
rs576795170 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057306 | TGGGCACTGAGGCCA[C/T]TAGGAGAAGCAAAAC | 9873 |
rs576801694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038522 | CTATGCAGCCATGAA[A/G]AGAATGAAATCTTGT | 9873 |
rs576840078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887725 | ACATTTTGAAATAAT[G/T]ATAGACTTACTAGTA | 9873 |
rs576850362 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054327 | AGTAAGCAAAGACAG[G/T]ACTGCCCAGACCCTT | 9873 |
rs576861419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913891 | AAGGACCTCTAAAAG[A/G]AGAACTACAAATCAC | 9873 |
rs576861824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031350 | GTGTGGTGGTGTGTG[C/T]CTGTAGTCCCAGCTA | 9873 |
rs576861927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039155 | CTATTCCTAAGAGTC[C/T]AGTTCAAGACTGTCT | 9873 |
rs576878862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920478 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 9873 |
rs576887988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959189 | TGGTTTCCCTGTTAT[C/T]CTTTCTTTTCCACTT | 9873 |
rs576892488 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144433 | GGCAGGAGAATAGCG[G/T]GAACCCGGGAGGTGG | 9873 |
rs576898220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908020 | CCATCCTGGCTCCCC[C/T]CACATCTGACTACCC | 9873 |
rs576912979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016013 | AGAAGTGAAAAAAAA[C/T]AATGATAGGCTGCAC | 9873 |
rs576913973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921301 | ATTTATTTTCTCTGC[A/G]TACAATGTGACATGT | 9873 |
rs576923864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032058 | AGAGAATGTGCTATA[C/T]AGTCTCAAATATTTA | 9873 |
rs576929292 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72959836 | TACTTCAAATTTCCC[C/T]GATTTTAAGTTTCTA | 9873 |
rs576949020 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948718 | TCGCCCAGGCTGGAG[A/T]GCAGTGGCACAATCT | 9873 |
rs576954355 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143911 | GTCTTGCTTTTTCTG[G/T]CTTCAAAAGTTAGCC | 9873 |
rs576955529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923621 | TCTTTGGTGAAAAGC[C/T]TACTCAAGTCCTTAA | 9873 |
rs576956499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852899 | CAGGAAGAGAAAACC[A/G]AATACTGCATGTTCT | 9873 |
rs576962560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73067619 | GCATTTATAAGACCT[A/G]GTTCTACATTAAAGA | 9873 |
rs576971136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853615 | AGATGGGGTTTTACC[A/G]TGTTGCCCAGGCTGG | 9873 |
rs577001990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053305 | AAAAGAAATGTGTGG[A/C]TCTACAACCTATTCA | 9873 |
rs577028778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068175 | TGAGATTTGGGTGGG[A/G]GCACAGGCAAACCAT | 9873 |
rs577040188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915322 | ATTAGTTCAACCATC[A/G]TGGAAGACAGGGTGG | 9873 |
rs577040324 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125852 | CTAAGAAAAACTATT[A/G]TATAAAACACTTCTT | 9873 |
rs577041443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101157 | TCAAAGAACCCTGAG[G/T]TTTAGTTCCGACCTG | 9873 |
rs577059117 | in-del | -/TTG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088050 | ACATGTGGCTAATTA[-/TTG]TTGTTGTTCCATTCC | 9873 |
rs577060083 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030057 | AAAAATCACAAAGCA[A/T]ACAAAGAAATAGGTA | 9873 |
rs577069314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72951769 | TCTGTTATTTTCCCA[C/T]TGATTTGAGGTTTAC | 9873 |
rs577074362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045041 | CTCCACTGCACTCCA[G/T]CCTGGGCGACAGAGC | 9873 |
rs577074844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062029 | GGAGACACCTCCCAG[A/T]AGGGGCCAACAGACA | 9873 |
rs577115071 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113570 | AACGGGGTTTCGCCA[C/T]GTTGCCAAGACTTGG | 9873 |
rs577116546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915801 | CCAGCCTGGGTGACA[A/G]AGCAAGACTCTGCCT | 9873 |
rs577127299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100040 | TCCCTGACGCACCCC[A/G]GAAGGCGTGTTCTTG | 9873 |
rs577133039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937839 | AAAAATGATTTTCTA[C/T]AGGAAATCATGTCTG | 9873 |
rs577134188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73062604 | ACATAAATGACCCGA[C/T]GGAGCTGAAATACAC | 9873 |
rs577138971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953337 | TTCCTTTTTCACAAT[C/T]TCTTTTTCAAAAAAT | 9873 |
rs577144109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045434 | TATATACCCAAAGGA[C/T]TATAAATCATGCTGC | 9873 |
rs577144670 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930591 | CTCTACCAAAAATAC[-/A]AAAATTAGCTGGGCG | 9873 |
rs577153417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72944500 | GGCACAAGACAGGGA[A/T]GCCCTCTCTCACCAC | 9873 |
rs577155394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952231 | ATATATATGGCCTAT[A/G]AAGGAAAACACTAAT | 9873 |
rs577160481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993522 | CCCAAATGTCCAACA[A/G]TGATAGACTGGATTA | 9873 |
rs577174857 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838075 | CTCCTTTCTATTAGT[C/T]TATGTGATGAACAAG | 9873 |
rs577175883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930610 | ATTAGCTGGGCGTGG[C/T]GGTGCCCATCCGTAG | 9873 |
rs577176316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938814 | TCTTATCAAGCTAAC[C/G]CAAGACTAATTTATC | 9873 |
rs577181480 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041630 | GTTGAGTTTCTTATA[A/T]ATTCTGGATATTAGT | 9873 |
rs577193472 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72945118 | GCCAAAAGAACAAAG[C/G]TGGAGGCATCACACT | 9873 |
rs577209182 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961891 | ACTCTATTTCAACTC[A/G]ATGTGTAAATGCCAC | 9873 |
rs577234184 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109647 | CAAATCATCTGCAAA[C/T]AAGCATAATTTGACT | 9873 |
rs577242230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885995 | TTCCATGGGGCTGTA[A/C]CAAAAACATGCTCAT | 9873 |
rs577246115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73042194 | AGCCTCCCAGTGTTG[A/G]GACTACAGGCATGCG | 9873 |
rs577248812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73093561 | CAAAATCCCTAAGAA[C/T]GTTCAAATTACCAAT | 9873 |
rs577266853 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018883 | TTTTAAAAATAATAG[-/A]AGTTTATTCCATACC | 9873 |
rs577278520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878582 | GTATTCAAGGACTAA[C/T]GGGGGTAATGTCAAA | 9873 |
rs577287749 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838534 | TAGGCATGAGGGCTG[C/T]CCCCCTCTTTGCTCC | 9873 |
rs577293793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984609 | TGTGCCAGATGAACT[A/G]CATGCTAGTTTGAAG | 9873 |
rs577306022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035166 | TATGTATGTATGTAT[G/T]TATGTATGTATGTAT | 9873 |
rs577335896 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879577 | GAAGATAAAAGAAGA[A/G]CCACATAGAACTTAT | 9873 |
rs577360999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968735 | TATACCCCATGAGCA[C/T]AAGGCCTGCTTACAG | 9873 |
rs577366815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73135314 | CAACAATATAATTCA[C/T]TTCATTTCACTGTGC | 9873 |
rs577373995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73086312 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 9873 |
rs577384747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025507 | GGTGGAGGGTGGGAG[A/G]AGGGAGATAATGAGA | 9873 |
rs577386367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73128483 | GCATATGACGCAAAC[A/G]CAGATAATGAAATAT | 9873 |
rs577396434 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72910360 | GAGAACGGGCCATGA[C/T]GACGATGGCGGTTTT | 9873 |
rs577402285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960996 | GTGGTTGCAGAGTAG[A/G]GTAAATAGAAAATGG | 9873 |
rs577404829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072992 | CTTTAAGCAAGGAGC[C/T]GCCCTTAAAGTCCAC | 9873 |
rs577423911 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142481 | CGGGGTTCGAGGGGC[C/T]GGTCCGGGCTGCCAG | 9873 |
rs577426379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134501 | AGAACATCCATAAAC[A/T]GACCTTGGAATCCAA | 9873 |
rs577449708 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127303 | AAAAAGATCAAATGG[A/T]ATGTTAAAACAAAGC | 9873 |
rs577450556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127406 | CTCCCGATCAACACT[A/G]ACAGAACATCTGCAG | 9873 |
rs577463372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72909185 | GGGATTGCAGGCACA[A/C]GCCGCCACGCCTGAC | 9873 |
rs577466780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72870440 | TTTTCCAAGAAAAGA[C/T]TGAATAGGCTCTACC | 9873 |
rs577467829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073930 | AAAGATTCAAACCAA[G/T]TCCAATCAAAATATC | 9873 |
rs577487802 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73142018 | AAGACTTGCCCCGGA[C/G]GGAGCAGGCCAGCGG | 9873 |
rs577522803 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72941242 | CTTGTTCACTATGTG[A/T]CCCCAGTAAATGACA | 9873 |
rs577528461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72862547 | GCAAGATCTATCTAC[C/T]GAAAACTACAAAACA | 9873 |
rs577528498 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122342 | AGAAGAAACATCAAG[A/G]CATAGACTCTGCTGC | 9873 |
rs577530253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066069 | CTGGGCAAGAAGAAC[A/G]AAGCTGGAGGCATCA | 9873 |
rs577536496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956500 | ATCAACAGGTTATTA[C/T]AATCAACTTTGACTT | 9873 |
rs577542402 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113681 | TTTGTACCCGTCCTT[C/T]TTGGGAAAGTTTTCC | 9873 |
rs577570736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73089145 | TCATTATAATGTATC[A/G]TATATATATCAAGAG | 9873 |
rs577575003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72957105 | AATTACATATGTATA[C/T]ATGTGCCATGCTGGT | 9873 |
rs577575028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949366 | GAGACAGGAGAATCA[C/T]TTGAACCCTGGAGGC | 9873 |
rs577591618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73009233 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 9873 |
rs577597121 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066794 | TGAGATATTATCTCA[A/C]GCCAGTTAGAATGGC | 9873 |
rs577603257 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948394 | TTTTTCAACATTTTA[G/T]TTGCTTTCCATTTTT | 9873 |
rs577636492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889257 | TGAGCCACCGCGCCC[A/G]GCTATAATTATGTCT | 9873 |
rs577639281 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881066 | ACTCTATGCAGCAAA[C/G]GAAACAAAAGAGTTA | 9873 |
rs577644520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934413 | TCGGCTCACTGCAAC[A/C]TCCACCTCCTGGGTT | 9873 |
rs577668910 | in-del | -/TTT | 0.00257532 | 0.0357915 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018518 | GTACAGATCTTGTCT[-/TTT]TTTTTTTTTTTTTTT | 9873 |
rs577671110 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72881812 | ATGTTCTCACTCATG[C/T]GTGGGAGCTAAAAAA | 9873 |
rs577677140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72971317 | TGAAGACTGCTGAAG[C/T]AGACAGAACTATAAA | 9873 |
rs577690532 | snp | C/T | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140841 | CCGGGGCCCCAGGGT[C/T]CGAAGTTAACGGTCA | 9873 |
rs577702522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132449 | AGCTAATAAGCAGCA[A/G]AGCTGGGTTTCAATC | 9873 |
rs577718262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028115 | CACAGGGGCACTGCC[G/T]ACTGGAGGGGTGAGA | 9873 |
rs577719179 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859618 | CAGGCATGCACTGGA[A/G]GTCTTGAAATATATC | 9873 |
rs577724524 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73117505 | TTAAGAGCTATAAAT[C/T]TCCTTTTGAATCATA | 9873 |
rs577731692 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950749 | TACTTAACTCCCACA[A/T]TATCATTTGGCTTCT | 9873 |
rs577753969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091484 | AACCCGGGAGGCAGA[C/G]GTTGCAGTGAGCCGA | 9873 |
rs577764138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115910 | GCCTTCATGGCAACA[G/T]GTAGATTAACATTTG | 9873 |
rs577784320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980232 | AAAGTTGAAATAACT[A/G]TTAAAAATAGTAGGA | 9873 |
rs577785694 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73020409 | TTGCCATTAGATGGC[C/T]CTTTAAAATTTTTGG | 9873 |
rs577786257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124584 | AACATGGTGAAACCC[C/T]GCCTCTACTGAAAAT | 9873 |
rs577787034 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047055 | TAAAAAATACTATTA[A/C]ATATAAAAGACAAGA | 9873 |
rs577797281 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72972566 | TATAAAGATTCCATG[C/T]AGGAGTTTGTTTTAA | 9873 |
rs577803952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964729 | ATTCTTGCTATTAGT[A/G]TCTGCCTTTCATATT | 9873 |
rs577821689 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092034 | AATGAGACTCACTCT[A/C]AAAAAAAAACAAAAC | 9873 |
rs577825018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980892 | GAGGCTCTTAAATGT[A/G]TATGATTAAACCAAC | 9873 |
rs577827269 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72904520 | TTTCATCTTTAAGCC[C/T]ACCTACCTCTTCCAC | 9873 |
rs577831994 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969607 | GAAGCATCGAAGATA[C/T]AAAAAACATTAAAAG | 9873 |
rs577846045 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081716 | TATCACAGACTTTCA[C/T]CTCAATTTTATAAAT | 9873 |
rs577863266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911659 | GTCCTCTTCAATTTA[C/T]TCCTTCCTTCCTTTT | 9873 |
rs577864620 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836732 | ACCTTTCTATATTAA[A/C]ACTTAGAAAACATAA | 9873 |
rs577866082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72865414 | AAAGATGCAGGCTCC[A/G]TAAGAGTGATGAGGG | 9873 |
rs577869126 | in-del | -/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837841 | GGCTGTCTGGGCCGG[-/T]TCTGCTGGCTTGGGA | 9873 |
rs577872080 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73016348 | CAACCAACCAACCAA[A/C]CAAACAAACAAAAAA | 9873 |
rs577877994 | in-del | -/AA | 0.0429648 | 0.14013 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73076954 | CTCTACTAAAAATAC[-/AA]AAAAAATTAGCCAGG | 9873 |
rs577879890 | in-del | -/ATAGATAAG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846088 | TAGATAGATAGATAG[-/ATAGATAAG]TAGTTACGATTACTT | 9873 |
rs577889963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982739 | GGACAGACATCTTCA[C/T]ATAGCTACTGAACAT | 9873 |
rs577890569 | snp | A/C | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839707 | GAAGGGAACATAACT[A/C]ATTTTTGCTGAGTTT | 9873 |
rs577892758 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912482 | TACATTCCACTTGGT[A/C]ATGATGAATAATCTT | 9873 |
rs577894014 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73007283 | TATCATATAAGATAT[A/C]TAGGAAAACCTAGAA | 9873 |
rs577895665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138678 | CAGTGGTGCCATCTC[A/G]GCTCACTGCAACCTC | 9873 |
rs577899514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72857905 | GGGTCTGGCCAACTT[A/G]GGTTTGAATGTTGAC | 9873 |
rs577901486 | snp | G/T | 0 | 0 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72905696 | ATGCAGTGTTTGGTT[G/T]TCTGTCCTTGTGATA | 9873 |
rs577917798 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077284 | ACCACAGAATATATA[C/G]AGATGGCAAATAAAC | 9873 |
rs577926829 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983527 | TAGTTGTGGCCAAAA[C/T]TGTAGTTAATAAAAA | 9873 |
rs577928643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974163 | ATAAACAACAGACGT[G/T]TATTTGGTTCATGGT | 9873 |
rs577950281 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858590 | TGGACACATAGAGGG[A/G/T]ATCAACAGACACTGG | 9873 |
rs577955608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73121234 | AGAAGATTATTTGCT[C/T]CTGCTTATTCCTCTC | 9873 |
rs577958549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071679 | GCACTCCAGCCTGGC[A/G]ACAGAATGAGACTCC | 9873 |
rs577984504 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012938 | TGATTTCTGCTACAA[G/T]TTCCTTGGTTCAAAT | 9873 |
rs577998859 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050749 | ATTCACTAACATGAG[A/G]AAAAAACCGTCTCAC | 9873 |
rs578010128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859367 | TGGCCATCTCGGTTA[C/T]CCCAATTGACTGTCA | 9873 |
rs578014184 | in-del | -/TTT | 0.0821764 | 0.185298 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850058 | TATGAAAGAATAGAG[-/TTT]TTTTTTTTTTTTTTT | 9873 |
rs578017680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106980 | TACCACCAGATATCC[C/T]GGACTCGACTTTTTA | 9873 |
rs578020336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997769 | GCAGTGGCACGATCT[A/C]GACTTCCTGCAATCT | 9873 |
rs578039780 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069633 | AAAGAATTAAAAATA[C/T]GTGAAAAAACCAAGA | 9873 |
rs578054597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998376 | GAAACCCTGTCTCTA[C/G]TAAAAATACAATAAA | 9873 |
rs578077615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943584 | TGAGACGGAGATGAA[A/G]GGCACAGAAATGGAA | 9873 |
rs578088788 | in-del | -/TTCT | 0.0023933 | 0.0345097 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932175 | TCTTATTGATTCCAC[-/TTCT]TAAATATTTACCAAA | 9873 |
rs578099122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72990753 | TGCCCACAAGAGAAA[A/G]CAGGAAAGATCTAAA | 9873 |
rs578101036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935831 | ATAAGGAAGTTTATG[C/T]CTGTAAATTACAAAA | 9873 |
rs578116833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898680 | CTTTTCTGGCTCTAA[C/T]GCTTATTAGCTGAGT | 9873 |
rs578135426 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104715 | CTGGGACCACAGGCA[A/C/T]GTGCCACCGCACCCG | 9873 |
rs578153226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912325 | TATGTTCCCTCTATA[C/T]CCAGTTTATTGAGGG | 9873 |
rs578162307 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100467 | CTCCTGGGTTCAAGC[A/G]ATTCTCCCGCCTCAG | 9873 |
rs578173534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084178 | GATGTTTACTGGACT[C/T]AACCAATGTAAGAGG | 9873 |
rs578176228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899441 | AGAACCACGAGATAC[G/T]ATTTCATATCCACTA | 9873 |
rs578179442 | snp | A/T | 1.69522e-05 | 0.00291132 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72889930 | TGGTCCCAGTTTCTG[A/T]TTCTAACTGTCGGCT | 9873 |
rs578188928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73029412 | CCAGAGAAAGATTTG[A/G]AGAGTAAATTACAGT | 9873 |
rs578190058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043662 | CAAGGCATATACATA[A/G]AAGAAATTTTCCAGC | 9873 |
rs578191374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035961 | CTTGACCTTGTGATC[C/T]GCCTACCTCAGCCTC | 9873 |
rs578194087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876222 | GTAGTCCCAGCTATT[C/T]GGGAGGCTGAGGTGG | 9873 |
rs578209399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73084819 | CAAACATAGGCATTG[G/T]AGAGTCAACAAAATG | 9873 |
rs578212525 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130121 | TCTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 9873 |
rs578215301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075057 | ATATGAAAAGTTCCT[C/G]TAATTCATTAATCAT | 9873 |
rs578235393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108952 | CATTCTTCTGCATAC[A/G]GATATTCAGTTTTTC | 9873 |
rs578245548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928640 | TTCTATGTGCTGTAT[A/G]GGTATTATTGCCAAT | 9873 |
rs578250873 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092816 | CATCGGAGTATACAG[G/T]AAAGGATTAACCCTA | 9873 |
rs745308193 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928254 | GGAAAAAAAATTCCA[C/G]AAAATTTTTTTCAAT | 9873 |
rs745310383 | snp | C/G/T | 0.000162995 | 0.00902633 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838917 | TCAGTCAGTTCCTGA[C/G/T]TCAGTATCTGAAGCA | 9873 |
rs745313133 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903240 | ATTTATTTTTTGAGA[C/T]GAGTCTCGCTCTGTC | 9873 |
rs745314714 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138997 | ATTGTAATTTTCAGT[C/T]AGAAAACAACAATCT | 9873 |
rs745317990 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73090957 | CCTGTCAACTACTAA[A/T]CTAATTTTTTGTCTC | 9873 |
rs745334765 | in-del | -/TTTATTTA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035696 | CTGAAATGTTCAGTT[-/TTTATTTA]TTTATTTATTTATTT | 9873 |
rs745341056 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100829 | CTCTTTCCCAAATAC[G/T]GGGCATTCCTTTTTT | 9873 |
rs745341664 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892266 | AGAGCTTTTCCCTTA[C/T]TTTTTATGTGTCTAC | 9873 |
rs745343426 | in-del | -/TTTG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72892597 | TTATGTTTTTGTGTT[-/TTTG]TTTGTTTTGTTTTTT | 9873 |
rs745343898 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848159 | CTTCTTAAAAGTCCA[A/G]TCTGATTTCAGGCCA | 9873 |
rs745363284 | snp | C/T | 5.66524e-05 | 0.00532194 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867945 | CCATTACTTGGTTCA[C/T]GGCACTCTTTAGCCA | 9873 |
rs745373823 | in-del | -/AT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884585 | TATATATAAAAGATC[-/AT]ATATATATATATAAA | 9873 |
rs745394107 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073825 | ATAAAAACTGTACAT[A/G]TGCAAGGATTTTTTT | 9873 |
rs745395795 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879594 | CACATAGAACTTATA[A/G]AGCTAAAAATATAAC | 9873 |
rs745404124 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022619 | GATGGAGAGACATTC[C/T]ATGTTAATGACTTGG | 9873 |
rs745413421 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125593 | ATCTGTAGTCTGAGC[C/T]ACTCAGGAGGCTGAG | 9873 |
rs745415736 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72969441 | AAAGAAAGAGAAAAA[C/T]ACTGAGAGGGACAGA | 9873 |
rs745422990 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930140 | CAATTGAGGGGCCAG[A/G]AGGAAAAAGCACTTA | 9873 |
rs745428864 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132221 | CATGAAACACGATAA[C/T]TTCCTTTTGTACCTT | 9873 |
rs745450412 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859312 | CCCCTTTGTCGAGTA[C/T]ATGCAAGCTATGTAA | 9873 |
rs745474324 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999706 | AAGCACCAGAGGTAG[G/T]TAAACTCTCTAAATA | 9873 |
rs745477329 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104386 | CTTCTCTTGCCTCAG[A/C]CTCCTCCAGAGTAGC | 9873 |
rs745485009 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72891002 | GGCTCACTGCAGCCT[A/C]AACCTCCGGGCTCAA | 9873 |
rs745505072 | snp | A/G | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841765 | CCAATTTTGCATTGC[A/G]CTTCACTTTTTCCTC | 9873 |
rs745518805 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72874279 | GCAGCCTCGAACTGC[G/T]GGGCTCAAGTGATCC | 9873 |
rs745524855 | snp | C/T | 1.6585e-05 | 0.00287962 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840903 | TGCCATATGAGGTCT[C/T]AGGAGTATGCCTTGA | 9873 |
rs745533675 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72981155 | TTAATGTACAGTACA[C/T]GAAAACTGAAAGTAT | 9873 |
rs745543789 | snp | A/G | 1.78551e-05 | 0.00298784 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73001083 | ATTCATCCGAGACTG[A/G]GCTACCTGCATTGTT | 9873 |
rs745549602 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73001982 | TATAAACACAATCGA[C/T]AATTTATAACAATGG | 9873 |
rs745563864 | snp | C/G | 0.000131852 | 0.00811842 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72887472 | GCTGCCACCTTACCT[C/G]TGCTTTACGAATATT | 9873 |
rs745582841 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051239 | AAAATCAGTTGAACC[C/T]AGGGGATTGAGGCTA | 9873 |
rs745593354 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965080 | AGGCATGAGCCACCG[C/T]GCCTGGCCAATCATT | 9873 |
rs745599806 | in-del | -/TTC | 6.55759e-05 | 0.0057257 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72983898 | TTGTCTGTAAACATT[-/TTC]TTAACTAAAAATTAA | 9873 |
rs745606453 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850993 | AGTCCCAGCTACTGC[A/G]AAGGCTGAGGCAAGA | 9873 |
rs745609042 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73097798 | TTTTAGTTTCTGTAA[A/G]GTAGTAGTATCCCCA | 9873 |
rs745614790 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954787 | AGGAAGATATTTACA[A/T]ACAAACATAGAAAGG | 9873 |
rs745622574 | in-del | -/CCC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051910 | CACACACACACACAC[-/CCC]ACACACCCCACACAC | 9873 |
rs745641459 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994468 | ACTCAGATGTTAAAT[A/G]ATTTACTCTGAGTCA | 9873 |
rs745645162 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048337 | AAGGTTCATGATAGT[C/G]TAGTACTGGCTTGTT | 9873 |
rs745660353 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72901773 | TATTCTAAGAAATCT[A/G]AAAGGAATTATAAAA | 9873 |
rs745661517 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081925 | AAAGCATTCAAGATC[A/G]GGCGCGGTGACTCAC | 9873 |
rs745663713 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72980098 | GTCTTCAACACAGAT[-/G]AAGTGGACAATATTG | 9873 |
rs745674562 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72886061 | CCCCACAACCAGTGA[A/C]GCACTTCCTCAAAAC | 9873 |
rs745677352 | in-del | -/TTC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115762 | GTCTTGAGGCAAAAT[-/TTC]TTCTTCTTCCAGATA | 9873 |
rs745683935 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999567 | TCAGGTGATCCACCC[A/G]GCTTGGCCATCCAAA | 9873 |
rs745685749 | snp | A/C | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839572 | GCAAGGTATACCTGG[A/C]AGGATTTGGGAATGA | 9873 |
rs745696727 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083505 | AGTGAGCCAAGATTG[A/C]GCCACTGTACTCCAG | 9873 |
rs745708763 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72855040 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGTTCAC | 9873 |
rs745718172 | snp | C/T | 0.000291146 | 0.0120619 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72902562 | TCACTGTCACAAGGC[C/T]GGAACTGGAAGGGCT | 9873 |
rs745730403 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133737 | GGCGGAGGTTACAAC[A/G]AGCCGGCATCGCGCC | 9873 |
rs745741726 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938085 | GAAATACATCCCCAG[C/T]ACCCTCAATGGCAGA | 9873 |
rs745755939 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73130331 | AGTACTATCATAGCT[A/C]ACTGTGGGCTCAAGC | 9873 |
rs745765804 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058482 | TAACACATGATAGAA[A/T]GATACATAGTTAAAT | 9873 |
rs745771397 | snp | A/G | 6.59609e-05 | 0.00574248 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72902632 | GAAGATTGTAGTCCC[A/G]GACCACCTAAAGAGA | 9873 |
rs745774006 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914694 | ATATGCAGAAAATTG[A/C]AACTGGACCCCTTCC | 9873 |
rs745787298 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112174 | TTCTTATAGGACAGG[G/T]CTGGTGTTGATGAAA | 9873 |
rs745820838 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953740 | AAGATGCCGCCTTAT[A/G]TTGTGTAGTCAGGGA | 9873 |
rs745828267 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72970305 | ACACTACCAAAACCT[A/G]ACAGTCTACAATCCA | 9873 |
rs745830695 | snp | C/T | 3.29652e-05 | 0.00405974 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843405 | GACCAAAACAAACTC[C/T]TAAAAATGTCACAAG | 9873 |
rs745841542 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72854291 | ACAAATGTTCACAGC[C/T]ACATTATTCACAAAA | 9873 |
rs745853043 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867630 | GATAGGCATCGATAA[C/T]CCAAATAGTGATAAC | 9873 |
rs745861138 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73011037 | CAGGTAGGTGTCAGC[A/T]GTGATTGTAGTGGCA | 9873 |
rs745862596 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041944 | TATTTATTTATGTTT[C/T]TGAGACAGAGTCTCA | 9873 |
rs745866223 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050977 | AGCATTTAGAAAGTT[G/T]TAAGCAATTTGACAT | 9873 |
rs745875391 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967790 | TATCTAATTTTTTTT[A/T]AAAAGAAGTGGGCAG | 9873 |
rs745880447 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73059684 | GAAACCGGCTAATAA[C/T]GAATTTTACTAAAAA | 9873 |
rs745896076 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72895875 | CACAAATTCTATCAC[A/G]GCCTTTTTCACATTT | 9873 |
rs745896145 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912284 | TCATTGTGGGTCTGT[C/T]ATACATGGCTTTTAT | 9873 |
rs745901140 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72946146 | GACTTGGAACCAACC[C/T]AAATGTCCAACAATG | 9873 |
rs745915996 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008221 | ATGCACACCTGTAAT[A/C]CCAGCTACTCAGGAG | 9873 |
rs745919391 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73107914 | CAATCGACATGGGTA[A/T]CTTTTGGATATATAC | 9873 |
rs745922317 | snp | C/T | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143494 | TGCACCCCACCACCA[C/T]ACATGAACCTTCCTG | 9873 |
rs745926550 | snp | A/G | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73144173 | TCATAGGCTTACTGT[A/G]TTAAATAGAATTTCT | 9873 |
rs745959500 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063699 | AGACAAAGAACGGTA[C/T]TACATATTGGTAAAG | 9873 |
rs745959636 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031416 | GGGAGGTGGAGGCTG[A/C]ATTGAGTTGTGACTA | 9873 |
rs745962873 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942667 | AATGGAAAATACATA[C/T]TTTATTAAAATTAAA | 9873 |
rs745966128 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056805 | TAGATTGACAAGGCC[A/G]GGCGCGGTGGCTCAC | 9873 |
rs745971826 | in-del | -/GTA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72994384 | GACTCTATGAAAAAG[-/GTA]GTAGTAGTAGTAGTA | 9873 |
rs745976958 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038958 | TTTGGCTTGACTTCT[A/G]TAATGACCCCCAGCC | 9873 |
rs746009828 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72934192 | AGTTTGAGAAGGGCA[C/T]GTATGATGAAGATGC | 9873 |
rs746010900 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094382 | ACATAATTAAACTTA[C/T]ATTTATTTTGATATA | 9873 |
rs746012468 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033357 | CACTCTAGTCCTGTC[C/T]AAAGATGATATGCAC | 9873 |
rs746052176 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73112863 | TAGAGATGGGGTTTC[A/G]CCATGTTAGCCAAGC | 9873 |
rs746054674 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911308 | ACTGCAGATAGGTAG[A/G]TTTGATTCTGGGTTC | 9873 |
rs746058811 | snp | A/C | 1.66018e-05 | 0.00288108 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849907 | AAGAAAAATTAGAAA[A/C]CATTGGCTAGTTTCC | 9873 |
rs746059344 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926401 | CCAGTTGCAGAGAGG[A/T]GTATTCTCTCTGCTA | 9873 |
rs746061284 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882573 | AAATTATAAATGTCT[A/G]AGGTGATAGATATCT | 9873 |
rs746081521 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72876739 | TTCTATATTCTTGTT[C/T]TATCAATTACTGAAA | 9873 |
rs746082711 | in-del | -/TTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872287 | TTTTTTTTTCTTTTC[-/TTT]TTTTTTTTTTTTTTT | 9873 |
rs746101129 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863032 | GGTTCAAGATACCTT[C/T]TTGCTTTAGCCTCCT | 9873 |
rs746103407 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122506 | CTCTTCAGAACACAG[C/G]AATGGCTACTTGTAA | 9873 |
rs746107271 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966008 | AAAGTAACAATGAGG[C/T]AAGAGAAGAAGATAA | 9873 |
rs746112798 | snp | A/C | 2.09028e-05 | 0.00323279 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867857 | ATATCCAAGAAAAGA[A/C]ATCGTACCGAGTGTA | 9873 |
rs746129435 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034613 | CAGCAAATTTATACT[A/C]ATAGTAAAGAAAAAG | 9873 |
rs746151468 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021564 | GCCTTTTGGAGGATG[A/G]AAGCTAGAAGGAAGG | 9873 |
rs746153399 | in-del | -/TTTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73035698 | GAAATGTTCAGTTTT[-/TTTT]TATTTATTTATTTAT | 9873 |
rs746153612 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006797 | GCAGCAGAAGCTCTG[C/T]TTCATTCACTGTTGT | 9873 |
rs746180524 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73116355 | CATATAATTTGATTG[C/T]TTGTACTGTCCTGTT | 9873 |
rs746184838 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72927093 | ACAAAACAAATGTAT[C/T]TCAGTCTTGCCCTCT | 9873 |
rs746187247 | snp | A/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant, intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842625 | CTCTCAGGTACCTGA[A/T]TCTCTCTCATCCATG | 9873 |
rs746194343 | snp | A/G | | | intron-variant, synonymous-codon | FCHSD2 | GRCh38.p7 | 11:73016545 | CATGTCACAGGGAAC[A/G]CAGCTGTCCATCTCC | 9873 |
rs746202780 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974631 | AATATGGCTACTGGG[A/G]CTGAGAAACAGAATT | 9873 |
rs746222333 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010761 | GGTAGGCCAGTCTTT[A/G]AGCCCCAGTAGAGGC | 9873 |
rs746238777 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73008326 | CCTGGGCGACAGACC[A/G]AGACTGTCTCAAAAC | 9873 |
rs746258410 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858210 | CAACTCCACTGGACA[A/G]AGAAGTAATCACAGT | 9873 |
rs746266455 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064901 | GTCCAGGACCAGACC[A/G]ATTCACAGCCAAATT | 9873 |
rs746271376 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960812 | CACTCTGATAATAAG[A/C]ATACAGGTAAAGAAA | 9873 |
rs746280031 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101417 | AGGGAGGTAAAGGCT[A/G]TACTCTTGTTGTTAT | 9873 |
rs746301927 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123630 | GACAATGTCATCACA[C/T]TATAATGGCAATATT | 9873 |
rs746316730 | snp | A/G | | | intron-variant, downstream-variant-500B | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72836515 | TTTTTTTTCCCATGG[A/G]AAAAGCAAAGACCGT | 9873 |
rs746324977 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040290 | ACTAGAAGCTGTAAT[G/T]GTTTCGCAGTCATGT | 9873 |
rs746340521 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987948 | AAACAATAAATACAA[A/T]AAAACAAATTAGAGA | 9873 |
rs746350196 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72917945 | CTGCAAAAAAGGCCA[C/T]TGGAATTTTGATAGG | 9873 |
rs746351724 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72863043 | CCTTCTTGCTTTAGC[A/C]TCCTGAGTAGCTAGG | 9873 |
rs746365924 | snp | G/T | 2.79045e-05 | 0.00373517 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72921904 | TCAGTCCGGCTGAAG[G/T]CTATTAAATAATCCT | 9873 |
rs746368005 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989323 | TTTGCCTAACAACCA[C/T]ACATTGAGAAATAAC | 9873 |
rs746373190 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72883353 | AAAAGTTTCCAATCT[A/C]GAAAATGAAAAGGTA | 9873 |
rs746389436 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973589 | TCAGAGTGGTAGTTA[C/T]AATCTGTTGAACATA | 9873 |
rs746400679 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960077 | TCTATAAAGAAAAAA[-/G]GTTTGGCTCACAGTT | 9873 |
rs746447650 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72991089 | CTATAAACACCTCTA[C/T]GCAAATAAACTAGAA | 9873 |
rs746447753 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843220 | TGGACGTGTGTGACC[A/G]ACTGTCCAAAGCGGC | 9873 |
rs746453333 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932141 | CTGCCTTGTCCCCCA[C/T]ATACTGTTAATTACC | 9873 |
rs746454215 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127697 | ATCATCAATTATTAA[A/G]GGGCAAATTATTCAG | 9873 |
rs746456952 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837875 | AAATAATGCCGGGGC[A/G]TCCCCAGTAGAGAAG | 9873 |
rs746465457 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72914815 | ATACCATTCAGGACA[C/T]AGGCATGGGCAAAGA | 9873 |
rs746470535 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73073833 | TGTACATGTGCAAGG[A/T]TTTTTTTTTCTTTTT | 9873 |
rs746480369 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025532 | ATGAGAAAAAAATAA[C/T]TAATGGGTACTAGGC | 9873 |
rs746488064 | in-del | -/TTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938178 | AGATTATGAAGGAGT[-/TTT]TTTTTTTTTTTTTTT | 9873 |
rs746524095 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858252 | CAAATACAACATGAG[C/T]AAGTTATCAAAGATG | 9873 |
rs746529474 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064641 | GTGGTGATATCCTTA[-/T]TATCAGTGGTGATAT | 9873 |
rs746539896 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73113226 | TCTCTGTGTTATCTC[A/G]AATTTCTTAGAGTTT | 9873 |
rs746555667 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73060015 | TATATATTCCTCTAA[A/C]GTATACCTCCTATCC | 9873 |
rs746558175 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104629 | GCTGGAGTGCAGTAC[C/T]GCAATCTCATCTCAC | 9873 |
rs746564626 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72915995 | ACCACATGTTCTCAT[C/T]TGTAAGTGGGAGCTA | 9873 |
rs746582575 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72848352 | TCTGTCTCTATACCT[A/G]CTGTTCTCTTTGCTT | 9873 |
rs746594006 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72900118 | AATTCTTAATTTATA[A/G]GAGAAAACACAGCTG | 9873 |
rs746595141 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72982402 | CAATTCGACTACAGC[A/G]ATGTGTGTGTTTGTT | 9873 |
rs746612703 | in-del | -/AC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999875 | CAATCAGACACACAC[-/AC]ACACACACACAAACA | 9873 |
rs746616980 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041657 | TAGTCCTTTATTAAA[C/G]GAATACTTGCAAATA | 9873 |
rs746626503 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73077245 | TTTAAAAAAAAATCA[A/G]TAAAATATTTGAACA | 9873 |
rs746626524 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73004867 | ATTTCCCAAGTTCTC[C/T]CTTCTCAAACCTCTA | 9873 |
rs746649659 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72893195 | TAGTAGAGATGGGGG[-/T]TTTGCTATGTTGGCC | 9873 |
rs746658418 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844934 | CTCATTTACCCTTGA[C/T]AGCTTTTCCAATGGA | 9873 |
rs746666197 | snp | C/G | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140486 | ATTCAAAGACATTAA[C/G]CACCAGGAGAGGTGA | 9873 |
rs746671526 | snp | C/T | 1.704e-05 | 0.00291885 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843365 | AAACAAGTTTACACA[C/T]ACAATTTAGACAGGG | 9873 |
rs746671914 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846919 | AATTTCAGTAAGTTT[-/C]ATAATATTATATGTT | 9873 |
rs746677663 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73125922 | TGGCTAATGCAAAAC[C/T]ACATTTCACAACAGA | 9873 |
rs746690584 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72930251 | TATCTAATAGCTGCC[A/G]AAACAATCTGTTGTG | 9873 |
rs746708450 | snp | A/C | 1.88386e-05 | 0.00306903 | synonymous-codon, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72988999 | CTCTCGTACTGCATG[A/C]GCCATCTGTTCAGTC | 9873 |
rs746712636 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880576 | GATCCCTATCTCTCA[A/C]CATATATAAAAGTCG | 9873 |
rs746716199 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956204 | TCCATGGACATAATG[A/T]TATAAATAAATAAAC | 9873 |
rs746724931 | snp | A/G | 1.67301e-05 | 0.00289219 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838905 | TTACGTAGTTTGTCA[A/G]TCAGTTCCTGACTCA | 9873 |
rs746736841 | snp | A/G | 6.30524e-05 | 0.00561446 | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841472 | TTGCTGAAGGAGACC[A/G]GGGAAAGTACAGGGA | 9873 |
rs746760902 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887824 | TGAGAGACCCCAAGG[C/G]AAACTGCTAAGCTGA | 9873 |
rs746763642 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939817 | AGAGATGGGGTTTCA[C/T]CATGTTTGTCAGGCT | 9873 |
rs746780734 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134869 | GTTTTTTTTGAGACA[G/T]AGTCTAGCTCTGTCA | 9873 |
rs746803382 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968048 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 9873 |
rs746804866 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72997755 | ATCCAGGCTGGAGTG[C/T]AGTGGCACGATCTCG | 9873 |
rs746812226 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72920040 | TTACTTAAAAACAAG[-/A]AAAGACTGAAAATAT | 9873 |
rs746812270 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72875592 | CCCTCCTGCCCTGGC[C/T]TCCCAAAATGCTGGA | 9873 |
rs746819034 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73054822 | GCTAGGACTACAGAC[A/G]TGTGGGCCTGGTGGC | 9873 |
rs746839937 | in-del | -/AC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134047 | AATCATATATGATAT[-/AC]AGTCACATCATGTAA | 9873 |
rs746843050 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72856117 | GCCATTACATTAATT[A/T]ATTAAAGTATCAAAT | 9873 |
rs746843392 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069205 | AGTCCCAGCCACTCG[A/G]GAGGCTGAGGCAGGA | 9873 |
rs746843587 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73032291 | TGGAGTACAACAGCA[C/G]AATCATTGTTCACTG | 9873 |
rs746858855 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72869256 | CCCTATCAAAAAAAG[A/G]AAATCAAGGCTTTTT | 9873 |
rs746866405 | snp | C/T | 3.3873e-05 | 0.00411526 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73015863 | TCTCTCTTCAGGTAT[C/T]GACTAGCCAACTTCT | 9873 |
rs746868656 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136199 | AAAAAAGAAGGGACG[C/T]AATGGGGAAGAACTA | 9873 |
rs746885224 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012712 | TGTATAATTCTTCAT[C/T]TCTCTCCCCCTGCTT | 9873 |
rs746892598 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924776 | CACTAGATGACACCA[C/T]TGAGCACTTCAAATT | 9873 |
rs746894251 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73055496 | TCTGATAAGAAATAA[C/G]ACAAAGTTTTAAACC | 9873 |
rs746899622 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043376 | TCCTATCCACTTTTC[G/T]GGGCAACCTGTCAAG | 9873 |
rs746919408 | snp | A/T | 1.64936e-05 | 0.00287168 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889979 | CAGAGATAAAAATAT[A/T]GCTATCCTTATTGTA | 9873 |
rs746923631 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871896 | TGTGCCCAACAGGTA[C/T]ATAATTTTGATTTCC | 9873 |
rs746925121 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73101134 | AAACATCTGAGATAA[C/T]TGGGGTTTCAAAGAA | 9873 |
rs746925497 | snp | A/G | 9.08884e-05 | 0.00674062 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73083659 | AGCCACGGAAAAGAA[A/G]TATACCTAGAATGGG | 9873 |
rs746925641 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73061235 | TTTCCCCCTACCCAG[A/G]GGAAGCCATGAGGGA | 9873 |
rs746931270 | in-del | -/T | 2.72676e-05 | 0.0036923 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984084 | GATATGAAAGCTGTA[-/T]TACCTTCATAATGTT | 9873 |
rs746932644 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098838 | AGGGGCAATTCTTCA[C/T]GACCTTGGATTTTGC | 9873 |
rs746975893 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956094 | GTGCTCAGAGAACAA[G/T]GGGGACATACTCCTA | 9873 |
rs746980300 | snp | A/G | 7.21267e-05 | 0.00600484 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902530 | ATGAAATGAAAATCT[A/G]TAATTCCCTTACAGT | 9873 |
rs747005831 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72935721 | TTGATATAAAGTAAA[A/G]TCAGAAACATATCAT | 9873 |
rs747011718 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73079060 | TGGATAATAGTTTAC[-/A]TGAGTGTGTTCACAA | 9873 |
rs747017439 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023269 | AAGCTGCAGATTAGG[-/A]AAAAAATACTTGCAA | 9873 |
rs747018165 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898579 | CATTTACCATCATAT[A/T]TAAAACTCAAAAATA | 9873 |
rs747029278 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095529 | ACATAACTGGAAATA[C/T]GATCTCCAATAAAAC | 9873 |
rs747033485 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953330 | TTCAAAATTCCTTTT[C/T]CACAATTTCTTTTTC | 9873 |
rs747035903 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72938669 | TGTCTGGAGAGGGTC[A/G]ATTTTCATCATTCTT | 9873 |
rs747059598 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73131059 | AGTCCAGTACCTGAT[C/G]TGCTACTTCCAGTTT | 9873 |
rs747075817 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037514 | CAAAATTATTTTTTG[-/C]CTCTGAGTTTTTGAT | 9873 |
rs747079073 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72954195 | GCAGTAGATGTGGGG[-/A]ATTTTTTTTTTTTTT | 9873 |
rs747082091 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989472 | CCCCATAATCTTAAC[A/T]AAGTCTCTCTTTATG | 9873 |
rs747102767 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72884449 | GGCCCAGAGGTAATA[C/T]AAATTTGGAAATAAT | 9873 |
rs747138187 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081392 | TGAGCCAAGATGGCG[C/T]CACTGGACTCCAGCC | 9873 |
rs747141256 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919707 | TCTCCAGTCCAACTT[A/G]TTCTTGGAAAAAAAC | 9873 |
rs747157317 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73118659 | GAGGATGTTTATCTC[C/T]TCATTACTGATTTCT | 9873 |
rs747161380 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022390 | TACCAAAAAACCTCA[G/T]GGAACTAATAACTGA | 9873 |
rs747177379 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73056956 | GGCATGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 9873 |
rs747177420 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913466 | TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGC | 9873 |
rs747227530 | in-del | -/ACACACA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73051909 | CACACACACACACAC[-/ACACACA]CCCCACACACACTGA | 9873 |
rs747232164 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72897597 | AAACCAAGGGACAAC[A/T]GTTGTCATTTTACAC | 9873 |
rs747257782 | snp | C/T | 7.61731e-05 | 0.00617096 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984040 | CCAACTTAAGTTGTT[C/T]TTGTTTTCAATGAAG | 9873 |
rs747261290 | in-del | -/TT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138606 | ATCTTGCACAGGAAT[-/TT]TTTTTTTTTTTTTTT | 9873 |
rs747276308 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002573 | GTAACTATTAATTTA[C/T]ACTTAAAATACATTT | 9873 |
rs747279943 | snp | C/T | 1.65888e-05 | 0.00287996 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72989146 | TAGTTTTCAGGCTTA[C/T]AGAAAATGACTTCAT | 9873 |
rs747280691 | in-del | -/TTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73045989 | CAATAATTTCAGTAA[-/TTT]TTTTTTTTTTTTTTT | 9873 |
rs747306146 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73002232 | AAGGAAAAAACTTGA[C/T]AAACTATGGTTTTCA | 9873 |
rs747313583 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72942642 | TTTTCTTCTGGTACT[C/T]TGGTAATCAAATGGA | 9873 |
rs747315735 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72977782 | GATCTAGAACTAGAA[A/G]TACCATTTGACCGAG | 9873 |
rs747317511 | snp | C/T | 1.65894e-05 | 0.00288 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867975 | ATGTGTCCACAGAAA[C/T]ACCAATCTGCTTTAG | 9873 |
rs747322191 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058045 | CGACCACGCCTGGCT[A/G]ATTTTTTGTATTTTT | 9873 |
rs747324551 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72962466 | GACAAAAACGTTTGA[A/G]AACCTCTGGTATAAG | 9873 |
rs747327330 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72906807 | TTGGTACCAGTGCCA[C/T]GCTGTTTTGGTTACT | 9873 |
rs747337739 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72898480 | CCTAATTCAAACTAT[A/G]AAATTCAAAATAAAA | 9873 |
rs747347756 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73064078 | AAAAGAATGGAAATC[A/C]TAACAGTCTCTCAGG | 9873 |
rs747361345 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72860372 | AGTTACCAAGATATA[C/T]GTTTATACTGGGTTA | 9873 |
rs747382501 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908343 | TGCTGCAATCAACAT[A/G]AGAGTGCAGATATCT | 9873 |
rs747406635 | in-del | -/ATGAG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73026813 | AGCAAGTGAGTTCTC[-/ATGAG]ATCTAATGGTTTAAA | 9873 |
rs747417682 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72943460 | ATCAGGAAAAAGACA[G/T]CACAGAACAATATGG | 9873 |
rs747418406 | in-del | -/CT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038831 | TGTACATGTATTCCC[-/CT]GATTCTAAAATAAAA | 9873 |
rs747429087 | in-del | -/CAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065799 | CCAACTTACAAGGGA[-/CAT]TGTGAAGGACCTCTT | 9873 |
rs747434588 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847366 | ATTCATTTGTTCATG[C/G]CTTCCATCATTCAAG | 9873 |
rs747441529 | snp | A/C | 1.65474e-05 | 0.00287636 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887441 | GTCATTAGACCTGGG[A/C]AAAATGCCACAATTA | 9873 |
rs747445193 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912604 | TTTGATGTGTCTTTG[C/T]CTGATTTTGGTATCA | 9873 |
rs747462611 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139063 | GCCTTAGTCATAAAC[C/T]CTGAAGACAGGTATA | 9873 |
rs747465670 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72837758 | CTTCCTTCCACGGAA[A/G]TGTCAGGGTAGTGGG | 9873 |
rs747466755 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73095173 | ACCTTGAGCGAGTTA[A/T]CTTTCCTGACTGTGC | 9873 |
rs747476149 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976062 | CACAAACCAGCTGAG[C/T]TGATTTCTGTAGATT | 9873 |
rs747483752 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72949950 | GTTTGAGAAACCACC[-/A]AATGCTAATGTTCAC | 9873 |
rs747486123 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867836 | TTCAGTGAAAATCAA[C/G]TTGTCATATCCAAGA | 9873 |
rs747497341 | snp | G/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839206 | AAATGAAACATTTCA[G/T]TGTGTCTTGGGTAGA | 9873 |
rs747506216 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72872656 | CCAAATAACATTCTA[C/T]TGTATGGATATACAT | 9873 |
rs747510209 | snp | A/T | 7.97099e-05 | 0.00631257 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841588 | GAAGGAGAGATCTGC[A/T]GCAAAGGGAAGCGAG | 9873 |
rs747521904 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73065033 | TCATCCTGATACCAA[A/G]GCCTGACAGAGACAC | 9873 |
rs747530320 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921459 | CGCTCCTTTTCCCTT[C/G]GTGCTCTTTTAGTAC | 9873 |
rs747538666 | snp | C/T | 1.64963e-05 | 0.00287192 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842609 | AATTCAACTGTCTCC[C/T]CTCTCAGGTACCTGA | 9873 |
rs747553851 | in-del | -/A | 2.4551e-05 | 0.00350356 | frameshift-variant, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838840 | CTGCTGGCCTTCGGT[-/A]GATTCTGTGTAGGTG | 9873 |
rs747555740 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72961292 | GCTGGAGTGGGATCA[C/T]AGCTCACTATAGCCT | 9873 |
rs747555867 | snp | C/T | 1.96845e-05 | 0.00313717 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889964 | CAATACAAGAGAGAA[C/T]AGAGATAAAAATATT | 9873 |
rs747567451 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873959 | TACTACCGTGCCACT[C/T]TAACCAATCAAATAT | 9873 |
rs747578526 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73050413 | CAGACATATATGTAC[A/C]TTTATAAACCATATA | 9873 |
rs747581257 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960945 | CATACCTCTCACTTA[A/C]TATGTTTTCCTACTT | 9873 |
rs747603871 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72859553 | TATGATAGATATGTA[G/T]GTATAGGGAAAAACA | 9873 |
rs747605545 | in-del | -/AC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72925387 | AAATTCCAGCTGGGT[-/AC]AGTGACTTGTGCCTA | 9873 |
rs747616519 | in-del | -/AGAGTATAATAAAAAAAAAAAAAAA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049675 | TGTACCCTAAAACTT[-/AGAGTATAATAAAAAAAAAAAAAAA]AAGAAAAAGGGGGAA | 9873 |
rs747631217 | in-del | -/CACACACAAACACACAC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999880 | AGACACACACACACA[-/CACACACAAACACACAC]ACACACACACTTTCT | 9873 |
rs747637868 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014507 | TCTCAAGACACCTTC[A/C]ATGATATCAGTAGGC | 9873 |
rs747655994 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958595 | ACGGAACAAAATCTA[A/T]TAAGTGAGTATTTCA | 9873 |
rs747659581 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73046208 | TCTTGCCCAGGCTAC[A/G]ATCGAATTCCTGTGC | 9873 |
rs747660564 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73080875 | CTTGAACCCAGGAGG[C/T]GGAAGTTGCAGTGAG | 9873 |
rs747666159 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134939 | AACCTCCACCTCCCA[A/G]GTTCAAGTGATTCTC | 9873 |
rs747681384 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956285 | AACTAAGAAAAGTAG[A/C]AGAAATGATGAAAAT | 9873 |
rs747688258 | in-del | -/ATA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73082630 | AATCTCTCATTATTT[-/ATA]ATGAGAATAAAAACA | 9873 |
rs747697773 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72847273 | AAAGTGTTGGGATTA[C/T]AGGCATGAGCCATTG | 9873 |
rs747704903 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940031 | GTGTTTTATGCGGCA[C/G]TGTTACAGCCTGTAT | 9873 |
rs747725923 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956443 | CTATTTGTCTCAATC[C/T]GTTGAGGCTGATACA | 9873 |
rs747730534 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127043 | TCTGTCTCAAAAGCA[A/G]ACAACAAAAAGAGTC | 9873 |
rs747748872 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72986130 | ATGCAGCCCAACTAC[G/T]TCCCCATTGTTAAAA | 9873 |
rs747774745 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73038731 | GCAAGGGTTGAAAAA[A/G]TAATTAGGCATGCTC | 9873 |
rs747796955 | snp | C/G | 1.70362e-05 | 0.00291853 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843141 | AAGAGTGCCTTGTTT[C/G]AGTCTTTACCACTGG | 9873 |
rs747802828 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882035 | CTGTAGTCCCGGCTA[C/G]TTGGGAGGCTGAGGC | 9873 |
rs747806521 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73010858 | CTGGTAGTGGCAGCA[A/G]TGAGCTGGGTGGGTG | 9873 |
rs747810192 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129082 | TTCACCATGTTAGCC[A/G]GGATGGTCTCGATCT | 9873 |
rs747886740 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72926722 | ACACAGGACAAGAAC[C/T]TGGGCAAAGGCACCA | 9873 |
rs747891045 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070964 | AAGTTGCAAACTGGC[A/G]TCCTTCAGATGGGAA | 9873 |
rs747893694 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012870 | TCTGCCAAATCATTT[C/G]CAAGTCCTCTGGCTT | 9873 |
rs747899089 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882180 | GGGCATGGTGGCTCA[-/T]GCCTGTAATCCCAGC | 9873 |
rs747924316 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73123053 | TAATTTTAAAAGATA[C/T]ATAGGTGAAGGATAA | 9873 |
rs747932275 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73104980 | TATCAACAGACCAAG[C/T]CACAGAGGCTGTCAT | 9873 |
rs747933553 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72966302 | GTAGCTGGGATTACA[A/G]GTGCCCGCCACCACA | 9873 |
rs747943617 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73023793 | ATAAACAAACTGTGG[A/T]ACATAATTATAATGG | 9873 |
rs747949146 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73138632 | TTTTTTTTTTGAGAC[A/T]GGGTCTCACTCTGTT | 9873 |
rs747957375 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021631 | TAATACCTGGGTAAC[A/G]AAATAATCTGTACAA | 9873 |
rs747974370 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73108070 | TCTCCACATCCTTGC[C/T]GGTGTTTGTTACTGT | 9873 |
rs747975143 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864373 | TGAGACTAGCCTGGG[A/C]AACATGGTGAAAAAT | 9873 |
rs747983595 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73071888 | GTGCTTAGAACAGTG[C/G]CTGACACATGATCTT | 9873 |
rs747986422 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72967671 | TGGGGGATAACAGAA[A/G]TGTTCTGGAATGAGA | 9873 |
rs748000242 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878036 | AAATAAAATATTAGA[C/T]AATATGATTAGGAAT | 9873 |
rs748017056 | snp | C/T | 0.000131802 | 0.00811688 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842763 | TCTTTGTTCAAGATA[C/T]GGATTATTGCTCCCT | 9873 |
rs748024059 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72889155 | GAGATGGGGTTTCAC[C/T]GTAACACATGTTAGC | 9873 |
rs748027354 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048020 | TCTATATTGTTTCTT[A/T]AAGTAGTACATACTG | 9873 |
rs748040988 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72912416 | TCATATAGTTTTTGC[C/T]CTTCACACAGAGTGA | 9873 |
rs748068558 | snp | C/T | 1.68315e-05 | 0.00290094 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:73015849 | TTACTCCAGGCCAAT[C/T]TCTCTTCAGGTATTG | 9873 |
rs748090882 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030955 | TTTTTTATCCTTTGA[C/T]CTAAGAAACTGTAGT | 9873 |
rs748109834 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72921578 | TCTCAAAGGCAATGC[A/G]CATGGCAATGGGCCA | 9873 |
rs748116610 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73100952 | TCAGAGCTCTCCTCA[C/T]ACAGACCCTTGTTTT | 9873 |
rs748118469 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72940641 | CCAGCCTGATAAAGC[A/G]CGCCGACCAGGCTGC | 9873 |
rs748120938 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73136383 | TGAGTAACATGGTAA[G/T]ACCCCATGTCTACAA | 9873 |
rs748122196 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72924863 | GACACTGCTGGTGTT[A/G]AGTCTGAATAAATTT | 9873 |
rs748124902 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908547 | TCACCAGCATCTGTG[C/T]TACTGCCTATCTTTT | 9873 |
rs748127248 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72999206 | TGACAGGTATACCCA[A/G]TATGTACTGAATATT | 9873 |
rs748134526 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922257 | GCTTAGGTGTAGGAG[-/T]TAAGTGAAATAATAA | 9873 |
rs748149969 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844798 | AAATAAGGCAAAAAA[A/G]GGGTCATTTTCAAGA | 9873 |
rs748153726 | in-del | -/CTT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73012245 | TTCTAAAATAGACTC[-/CTT]AAGTGTGTGGGCGGG | 9873 |
rs748156748 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73017396 | TACACGTAACTAAAA[A/T]GAACACAATGCTGAA | 9873 |
rs748157496 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72993799 | GCATTTGGAGATATA[C/T]CTAATGTTAAATGAC | 9873 |
rs748158131 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72937894 | CACCATGGGAAATAC[A/C]GAACATAAGATCAAA | 9873 |
rs748186428 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033469 | GTAATCTCTAAGGTC[A/T]CCGCTTATAAACATA | 9873 |
rs748188568 | snp | C/G | 4.70267e-05 | 0.00484883 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841569 | GGAGGCGTGTGGCTT[C/G]GGGGAAGGAGAGATC | 9873 |
rs748212723 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73133653 | ATTGAAAAATTAGCT[A/G]GGTACGGTGGCGGGC | 9873 |
rs748231538 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088200 | TCATACCATATTTTT[-/G]TTGTATCTTTCCTAC | 9873 |
rs748233824 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911695 | TTATTATTATTATAC[-/T]TTTAAGTTTTAGGGT | 9873 |
rs748242433 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72907031 | TATGGCCATTTGTTT[C/G]CGTCCTCTTTTATTT | 9873 |
rs748269627 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73003250 | CTTTCATTTCCTCAA[C/G]TGGCAAATGGAGAAA | 9873 |
rs748278333 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73031133 | GAAAGAAGACGACTA[C/T]TATTTGATCTGTTAT | 9873 |
rs748286462 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73066676 | AAAAGTAGGCAAAGG[A/G]TATGAACAGACAGTT | 9873 |
rs748286547 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73040711 | TCATCTCAAACATTT[A/G]TCATTTCTTCATGTT | 9873 |
rs748302390 | snp | C/T | 9.55795e-05 | 0.00691235 | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140137 | CTTTCACCTAAAATA[C/T]ACCATATATTTATGA | 9873 |
rs748303731 | snp | A/C | 1.66957e-05 | 0.00288922 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842584 | GAGCAATTTTCTTTA[A/C]ACATCTTTTAATTCA | 9873 |
rs748305830 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72899939 | TGTCATTAATTTACC[A/G]TATGACTCTGGACAA | 9873 |
rs748313207 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73119195 | TAGTCCCAGCTACTC[A/G]GGAGACTGAAGAGGG | 9873 |
rs748317204 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72922431 | AATATTAAAAAAAGA[A/G]AAGTGACTCAGAGAT | 9873 |
rs748320406 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132224 | GAAACACGATAACTT[C/T]CTTTTGTACCTTGAA | 9873 |
rs748341902 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72853875 | CCTAAAACTGACCAT[C/G]AACAACAAATAATCC | 9873 |
rs748352981 | snp | G/T | 1.97556e-05 | 0.00314284 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72902676 | TTAGGTCTTTAATGA[G/T]GTTAAAATGTCCAAT | 9873 |
rs748362949 | in-del | -/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72968246 | ACTTTCTGAACAAAT[-/G]GAAAATAATTACAGA | 9873 |
rs748389618 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73030102 | GAATGCCATTAGTTT[G/T]AAAATATTTTTGCCT | 9873 |
rs748389860 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73092366 | GCTGATCTCAAACTC[A/C]TGGCTTCCAGTGATT | 9873 |
rs748396336 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72974983 | AAGAGCCACAACTCA[A/G]AATAAAAAAGATGAG | 9873 |
rs748404241 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948446 | CATGTAGACAAATAT[A/C]ATAATAGATATTTAT | 9873 |
rs748445392 | snp | C/T | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72839342 | GCTTTATTCTGTAGG[C/T]AAAAGAGGAGTTTTT | 9873 |
rs748452986 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73069920 | AAAACAATAACTAAA[C/T]ATGTAAAAAAACAGA | 9873 |
rs748453353 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73043088 | GAACTTCTGCCACAA[C/T]GCTGAATAGGAGTGG | 9873 |
rs748456874 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72950465 | TTTTATATAGTTTTA[A/G]CTCTTAAGTCTTTGA | 9873 |
rs748459634 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73106756 | GTATCACAATTGCTT[A/C]AAGTATTCAGTACAG | 9873 |
rs748467138 | in-del | -/TTTAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948514 | AGACAAAGAATATAG[-/TTTAT]TTTAAAGCATTTGAT | 9873 |
rs748471116 | in-del | -/TATTTATA | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903199 | ATTTATTTATTTATT[-/TATTTATA]TATTTATATATTTAT | 9873 |
rs748481080 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73006327 | GTACAAAACTAAATT[A/C]TTGATTTCCCTAAAA | 9873 |
rs748481456 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73075584 | ATGGTGGGAGGCCAA[C/G]GAGGACGGATCACTT | 9873 |
rs748484057 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871242 | ACTAGTCCTCCAAAC[G/T]CTAAAAACCAAGGCT | 9873 |
rs748484166 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72838174 | ACGAAGGACACTGTT[A/G]TTTTAAGTCTGTTAG | 9873 |
rs748484486 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894564 | ATCTTATTCTTTATG[A/G]AGTATATTAATATAT | 9873 |
rs748489534 | snp | C/T | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140560 | CCAATGACCAATATT[C/T]ACACAATCATGATAA | 9873 |
rs748528598 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72932555 | TTTTTTGCCTCTGAG[C/T]TTTCACACAGGCTTT | 9873 |
rs748530013 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73099731 | TGGTTGGGGCTGTCA[A/G]GCCGGACCAAAAAGG | 9873 |
rs748539414 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72880967 | GCTTCTGGACATTGG[A/T]CAAGGGAGATTTTTA | 9873 |
rs748549568 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73037500 | CTCATAATTATGCCC[A/C]AAATTATTTTTTGCC | 9873 |
rs748572936 | snp | G/T | 1.65326e-05 | 0.00287507 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72984244 | AAAATAAAATAATCA[G/T]TGCAAACTGATATTG | 9873 |
rs748577324 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73127900 | CAAGAGTTTGAGACC[A/G]GCCTGGCCAACATAG | 9873 |
rs748581735 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72885342 | CTATATTCAACATTT[G/T]TGATAAGAAAACTAT | 9873 |
rs748587201 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72861183 | AGAGAGGAGACATGA[A/C]CAATATCAGGAATGA | 9873 |
rs748617827 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73018743 | CAAATTTTTTAATAA[C/T]TGTATCAGATTTCTG | 9873 |
rs748626464 | snp | C/T | 3.80069e-05 | 0.00435913 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72988974 | CATACTTTGCCTCGA[C/T]GTCAGCTTTCTCTCG | 9873 |
rs748628419 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068173 | GATGAGATTTGGGTG[C/G]GGGCACAGGCAAACC | 9873 |
rs748651242 | in-del | -/AG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73122558 | GCATGGCTAAGGAAT[-/AG]AGACTTAAATTTCCT | 9873 |
rs748665720 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053574 | GTAGTATACAAATAC[A/G]TTATCTCTTGTGAGT | 9873 |
rs748666776 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908489 | GTTGTACTAATTTAC[A/C]TTCCCAGCAACAGTA | 9873 |
rs748678642 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841514 | CTGGGCTGGGGTAGG[A/G]GCTGCTGGGAGGCTG | 9873 |
rs748685313 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139380 | TCTTTGTTGAACTGT[C/T]AGTCTGTATTACAAG | 9873 |
rs748686088 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72960535 | ACTGATAATGGATTA[C/T]GGCACTTGAGCCTAG | 9873 |
rs748700554 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72931159 | GGAGTGTAGTGGTGC[A/G]ATCAGGCTCACTGCA | 9873 |
rs748704300 | in-del | -/TG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72873531 | CCCCATTCTGTGGGC[-/TG]TCTTTCATTTTCTTG | 9873 |
rs748707251 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73036472 | TAATTTCATTAGTCA[C/G]TTTGAGCTTTAGTTT | 9873 |
rs748710085 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73005006 | CTCCTATTACTTGCA[C/T]GAACTACCTGTGCTC | 9873 |
rs748724466 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952471 | CTGGGATTACAGGCA[A/T]GTGTCACCACGCCCA | 9873 |
rs748755228 | snp | C/G | 1.85197e-05 | 0.00304295 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841002 | TTTACTTGAGTTGTT[C/G]AGCAATAATGCTGAT | 9873 |
rs748757363 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73049873 | GCACAAAAGGACCAT[A/T]AAAAAAAAATTGTTT | 9873 |
rs748769706 | in-del | -/TAAAGAGAAAATAAAA | 7.15999e-05 | 0.00598288 | splice-acceptor-variant | FCHSD2 | GRCh38.p7 | 11:72902640 | TAGTCCCGGACCACC[-/TAAAGAGAAAATAAAA]TATCTTTAGGTCTTT | 9873 |
rs748785977 | in-del | -/AGGAAACTTATCAGTAACAAGAATTTCATTGTCCCAAGAAGAAAAT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73070085 | TGGCAAAAGTAAAAA[lengthTooLong]ATAGGGTAAACAAAG | 9873 |
rs748809019 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047863 | GGTGAGCTAATGACT[C/T]TGTTATCTCATTTAA | 9873 |
rs748814318 | in-del | -/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73025007 | CAGAAGTTGGCAAGG[-/T]CGTGGAGAAAAAGAA | 9873 |
rs748824328 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73033545 | GGAGGAATTATAGGG[C/T]GCTACACAAGACATC | 9873 |
rs748876562 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73137816 | AGCAGGGGGAAGAAA[C/G]AGGAAGGATGCATGG | 9873 |
rs748882724 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73014679 | GCTTCAATACTAAGT[A/T]CTCAATTACCCTGGA | 9873 |
rs748882925 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72871027 | GGCTGGCAGAAATAG[C/T]AGAGATTGAGAATAA | 9873 |
rs748902180 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73132092 | TGCTGATACCCATCC[A/C]GCAAGTTCTATGCAT | 9873 |
rs748903589 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028453 | TATCAAATGCCTGTA[C/G]CCCCATTGTATCTTG | 9873 |
rs748915265 | snp | C/T | 3.32298e-05 | 0.004076 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72887609 | AATAATGATGACTGT[C/T]TTTTACTTTTCATCT | 9873 |
rs748918413 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72903894 | TACTGCTTCCCTCCC[C/G]CTCACTCCACCAACC | 9873 |
rs748926730 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73115765 | TTGAGGCAAAATTTC[C/T]TCTTCTTCCAGATAC | 9873 |
rs748931317 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978635 | GCGATTTCCCTGATG[C/G]TGTTCTCATGATTGT | 9873 |
rs748938354 | in-del | -/AAG | 1.75007e-05 | 0.00295805 | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840976 | TAAGGGAGAAAACCA[-/AAG]AAGCTCATTTTACTT | 9873 |
rs748938816 | in-del | -/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73015373 | TACATTAGAAAGTTT[-/C]CCCCCTAGTCTCACA | 9873 |
rs748950790 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919164 | CTTCCCTTTAGGTTG[A/C]TTTCAGCAGCATAGC | 9873 |
rs748966822 | snp | C/T | 0.000164788 | 0.00907562 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72842792 | CTCAGGAAAAGATAA[C/T]TCATCATCTGTCTGG | 9873 |
rs748974353 | snp | A/G | 3.29576e-05 | 0.00405928 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843431 | ACAAGAAAGGGCGAT[A/G]TGAGCAAAGGAATAT | 9873 |
rs748986412 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879540 | TTTAAAGAAAAACAT[A/G]AAGATAAATAGGAAT | 9873 |
rs748991921 | in-del | -/TTGT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73098313 | TCTTTGATCTACTCG[-/TTGT]TTAAGAATATGTTTA | 9873 |
rs748999134 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72858076 | ATGTTTGGTGCATAG[A/G]AGGTACTTAATAAAG | 9873 |
rs749003948 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72958746 | GTCACTTAAAAGTAA[C/T]CAGATTTAAGAAAAA | 9873 |
rs749005398 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72998155 | TCTAACAGCCAAAAA[A/G]TCATAAATGAGAGTT | 9873 |
rs749030704 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73048158 | CAAACTGCAAAAAGT[A/G]AAAATCTGACCCAAA | 9873 |
rs749038308 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911889 | TTTGGTTAATTCCTA[C/T]GTATTTTAATGTATT | 9873 |
rs749044301 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72913660 | TTTCTGTGGTATTGG[C/T]TGTAATGTCTCCTTT | 9873 |
rs749056876 | snp | C/T | 2.26078e-05 | 0.00336205 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72921872 | ATGTGTTCTGCACAG[C/T]TTGGCATGTTTCTAG | 9873 |
rs749069973 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72952482 | GGCATGTGTCACCAC[A/G]CCCAGCTAATTTTTA | 9873 |
rs749073358 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73109911 | TATCATGAAGGAATA[C/T]TAAATTTTATTAAAT | 9873 |
rs749080820 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111764 | GTGTATCTGTTATAT[G/T]ATTTTTGATTTGAGG | 9873 |
rs749089733 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73111720 | ATTTTCTCTGGTGGG[A/G]TGTTTTAATTTCTTG | 9873 |
rs749124128 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72953586 | ATCAAGAGTCTACTA[C/T]TTGTCAGACATTATT | 9873 |
rs749124405 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72846732 | TCTCCAAATTTCCTG[C/T]ATTTCTTTTAAAACA | 9873 |
rs749126909 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72852718 | ATTGCAGCACTATTT[A/G]TACTAGCGAAGACAT | 9873 |
rs749138038 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72866415 | GCTGGGATTATGGGC[A/G]TCTGCCACCATGCCT | 9873 |
rs749149007 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73072537 | TTTCTAAACACTGTT[A/G]TAAGATAAGGAAAAA | 9873 |
rs749162724 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73034810 | ACCAGAACTTCGAAG[C/G]AGCAAAAGAAAATAA | 9873 |
rs749162889 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73021728 | ACTTAAAAAAAAAGC[C/T]CATTCATGACAGAAT | 9873 |
rs749169818 | snp | C/T | | | upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73143489 | AGCAGTGCACCCCAC[C/T]ACCACACATGAACCT | 9873 |
rs749180350 | in-del | -/CT | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73047831 | AATATTTGCTAATGA[-/CT]GTATATACAAATGAT | 9873 |
rs749180515 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72878370 | TAAAAAAAGTTATCC[A/C]TAGCTCTAACAACAA | 9873 |
rs749185922 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73081509 | GTATTAAAAATTTTT[A/T]AAGCATATCATAGAC | 9873 |
rs749195782 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72964921 | CAGCCTCCCGAGTAG[C/T]GGGGACTACAGGCGC | 9873 |
rs749221039 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72928479 | CTCTTGGCCTAGAAT[A/G]TCCTTCCCCCCTTCT | 9873 |
rs749225080 | in-del | -/AG | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72882724 | AGTGCCTAAATAAAT[-/AG]AGAGACACATCATGT | 9873 |
rs749233608 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850648 | GTGAGCCACCGTGCC[C/T]GGCCAGGACAGAGAT | 9873 |
rs749239138 | snp | A/C | 6.78288e-05 | 0.00582321 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73000984 | GAACAGAAATAAAAA[A/C]AATACCCTTTTTAGT | 9873 |
rs749241529 | snp | C/T | 1.67203e-05 | 0.00289134 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72849705 | ATACAGTCATGTGTA[C/T]CTTCAGAGTTAATCA | 9873 |
rs749265906 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73124108 | CGTTCACGTCCTTTG[C/T]AGGGACATGGATGAA | 9873 |
rs749273168 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72879383 | TCACTATGTCTAGAT[G/T]CAGTAAAAACTTAGT | 9873 |
rs749285691 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73022571 | AGTCCATAATACTAA[C/T]GAAAGAAAGAAAAGA | 9873 |
rs749292142 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73057057 | CACTGCACTCTAGCC[C/T]GGGCGACAGAGCAAG | 9873 |
rs749310257 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73068989 | CACTGCACTCTAGCC[G/T]GATGACAGAGCAAAA | 9873 |
rs749320299 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908605 | TATAATATCTTACTG[C/T]AGTTTTGATTTGCAT | 9873 |
rs749326905 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72939396 | GGTTTTTAAATTATT[A/C]AACAAAAATTAAGTT | 9873 |
rs749327485 | snp | A/C/G | 0.000165817 | 0.00910418 | intron-variant | FCHSD2 | GRCh38.p7 | 11:72867861 | CCAAGAAAAGAAATC[A/C/G]TACCGAGTGTAAAGT | 9873 |
rs749336301 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72894769 | AAAACTCACTTGAGC[C/T]AAAATGTGATTTGAA | 9873 |
rs749348800 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73120445 | CAGAAACATATGAAG[A/T]TAGGCCAGGAGCAGT | 9873 |
rs749376981 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72911002 | TTTTTAACTTGATGT[C/G]ATCCCACTTGTCCAT | 9873 |
rs749379374 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73058918 | CTTTTTTGGATCACT[G/T]ACCAACCAGAAATAT | 9873 |
rs749390574 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73091700 | TGTGGTCTTTTCCAC[G/T]TGGAATTTCCTCCCG | 9873 |
rs749405496 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73053961 | ATAATTCACTTTTAT[C/T]GTATTTTACAAAAAT | 9873 |
rs749406715 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73139750 | CAATTCCGTGGAAAG[A/G]TTATTTAAACAAGAA | 9873 |
rs749417568 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72948877 | TCACCACGTTAGCTA[A/G]GATGGTCTGGATCTC | 9873 |
rs749420617 | snp | G/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72965709 | CACTCTTTCCCATTC[G/T]ATGTACACCCCTCAC | 9873 |
rs749443033 | snp | C/T | | | intron-variant, upstream-variant-2KB | FCHSD2 | GRCh38.p7 | 11:73140796 | GGAGAACAGCAAATG[C/T]CTGCTGGCCAGAGAG | 9873 |
rs749466926 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72995897 | ATTTATCCTAAGAAA[A/C]AAATTTAAAAAGTTA | 9873 |
rs749469386 | snp | A/G | | | intron-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72840700 | TAGATTAAATGTCCC[A/G]AGATGAGTTGATTTC | 9873 |
rs749471907 | snp | C/T | 2.43579e-05 | 0.00348975 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72867929 | TCATTTTCCAGTTCT[C/T]CCATTACTTGGTTCA | 9873 |
rs749472013 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72978259 | GCACATGTATACATA[C/T]GTAACAAACCTGCAC | 9873 |
rs749472014 | snp | C/T | 0.000101942 | 0.00713867 | intron-variant | FCHSD2 | GRCh38.p7 | 11:73140022 | TTGAACTATTTACTA[C/T]AGCCTTACCTCATAT | 9873 |
rs749481772 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72976695 | GTATGGTACTGGCAT[A/G]AAAATAGACTCACAG | 9873 |
rs749487064 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72908870 | TGTTGCCCAGGCTGG[C/T]CTCTAACTCCTGGGC | 9873 |
rs749487380 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72923076 | CTGGCTTCTGTTGCC[C/T]AGCATAATATTTTCA | 9873 |
rs749504440 | in-del | -/TTATC | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72918239 | CTGATTTTTGTGTTT[-/TTATC]TTATATGTTGCTAAA | 9873 |
rs749518810 | snp | A/G | 0.000156928 | 0.00885659 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841560 | TGGAGGCAGGGAGGC[A/G]TGTGGCTTGGGGGAA | 9873 |
rs749521135 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73063544 | GTATTCAGGAGACCC[A/T]TCTCATGTGCAAAGA | 9873 |
rs749521440 | snp | C/T | 2.07303e-05 | 0.00321943 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72841494 | GTACAGGGAGCTCCT[C/T]TTATCTGGGCTGGGG | 9873 |
rs749530121 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73134730 | CTTTGGTGAAACTCA[C/T]GTTAACGGTTTGAAA | 9873 |
rs749539444 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73019080 | ATGAGGAAAAGATCA[A/T]CTGGTATTTTCTCAA | 9873 |
rs749556858 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73028546 | ATGAGACTTTGGCCT[C/T]GGACTTTTGGGATAA | 9873 |
rs749567911 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73129392 | TTCGTCCATACTTAC[A/T]GCCGCCCCCGCATTG | 9873 |
rs749593246 | snp | A/G | 1.90391e-05 | 0.00308532 | intron-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD2, ATG16L2 | GRCh38.p7 | 11:72843115 | CAGTTTAGGTCAAAC[A/G]TGACCAAATAAAGAG | 9873 |
rs749606299 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72919628 | AGAAATTGTTAAGTG[C/T]GTGTAAAATATTAGC | 9873 |
rs749607211 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73094190 | CACTCCAGCCTGGGC[C/T]ACAGAGCAAGACTCT | 9873 |
rs749633750 | snp | A/C | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73027438 | AGCAAAGCATTCAAA[A/C]TGTAACCTGGCTTTT | 9873 |
rs749638461 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73041103 | CCATTGTGTATATAA[A/T]CCATATTTTCTTTAT | 9873 |
rs749644671 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72987818 | CAAGTTTCTAAAAAC[A/G]ACTATGACAGTATAT | 9873 |
rs749657024 | snp | A/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73039077 | ATAATAATTGCAGAA[A/T]CACTGTTTATTTTTA | 9873 |
rs749666335 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72956923 | ATCATGCACTTCTTC[A/G]TGTGATACATAGAGA | 9873 |
rs749705988 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72973379 | TCTCAAAAAAAAAAG[A/G]AAGAAAAGAAAAGAA | 9873 |
rs749706606 | snp | C/T | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72844402 | ATGGTTTGGATTTCT[C/T]ATGCTCCAACTTAAC | 9873 |
rs749715322 | in-del | -/A | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:73088595 | AACATATAATGTTTG[-/A]AAAAAAAAGTCCTTT | 9873 |
rs749730627 | snp | A/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72850188 | GTGCCTCAGTCTCCC[A/G]AATAGCTGGGATTAC | 9873 |
rs749733650 | snp | C/T | 2.32275e-05 | 0.00340781 | missense, nc-transcript-variant | FCHSD2 | GRCh38.p7 | 11:72984093 | GCTGTATTACCTTCA[C/T]AATGTTAACTAAATC | 9873 |
rs749738163 | snp | C/G | | | intron-variant | FCHSD2 | GRCh38.p7 | 11:72864016 | TTATCTTACCCTTAT[C/G]TCCAACATCATTATT | 9873 |