Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 14 | |||
rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 9 | |||
rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 9 | |||
rs2545801 | 5 | 177414338 | intron variant | T/C | snv | 0.56 | 3 | ||||
rs2731672 | 5 | 177415473 | intron variant | T/C | snv | 0.66 | 3 | ||||
rs16860992 | 1.000 | 0.080 | 3 | 186676249 | intron variant | G/C;T | snv | 2 | |||
rs2050190 | 1.000 | 0.120 | 6 | 32371299 | intron variant | A/G | snv | 0.35 | 2 | ||
rs2287694 | 5 | 177433292 | intron variant | T/C | snv | 8.5E-02 | 2 | ||||
rs13177732 | 5 | 177429924 | intron variant | T/G | snv | 0.16 | 1 | ||||
rs1624230 | 3 | 186721146 | intron variant | C/A | snv | 0.42 | 1 | ||||
rs1624569 | 3 | 186732280 | intron variant | T/C | snv | 0.38 | 1 | ||||
rs2469184 | 15 | 86648746 | intron variant | A/G | snv | 0.54 | 1 | ||||
rs266723 | 3 | 186729258 | intron variant | A/C | snv | 0.44 | 1 | ||||
rs3856930 | 3 | 186740533 | intron variant | C/T | snv | 0.27 | 1 | ||||
rs4253304 | 4 | 186252417 | intron variant | G/C | snv | 0.36 | 1 | ||||
rs5030023 | 3 | 186726855 | intron variant | G/A | snv | 0.20 | 1 | ||||
rs5030028 | 3 | 186727965 | intron variant | C/T | snv | 0.23 | 1 | ||||
rs7381103 | 5 | 177411311 | intron variant | C/G | snv | 0.11 | 1 | ||||
rs2228243 | 1.000 | 0.080 | 3 | 186677324 | missense variant | A/G;T | snv | 0.20; 4.0E-06 | 2 | ||
rs9898 | 0.925 | 0.160 | 3 | 186672838 | missense variant | C/T | snv | 0.38 | 0.43 | 2 | |
rs1042445 | 3 | 186677647 | missense variant | C/A;T | snv | 0.27 | 1 | ||||
rs710446 | 0.925 | 0.120 | 3 | 186742138 | missense variant | T/C | snv | 0.42 | 0.44 | 1 | |
rs2289252 | 1.000 | 0.040 | 4 | 186286227 | non coding transcript exon variant | C/T | snv | 0.35 | 2 | ||
rs7447593 | 5 | 177397136 | non coding transcript exon variant | C/G;T | snv | 2 | |||||
rs1621816 | 3 | 186721384 | non coding transcript exon variant | T/C | snv | 0.32 | 1 |