Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs266723 | 3 | 186729258 | intron variant | A/C | snv | 0.44 | 1 | ||||
| rs5030062 | 3 | 186736391 | non coding transcript exon variant | A/C | snv | 0.35 | 1 | ||||
| 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 | |||
| rs1801020 | 1.000 | 0.040 | 5 | 177409531 | 5 prime UTR variant | A/G | snv | 0.65 | 0.67 | 3 | |
| rs2050190 | 1.000 | 0.120 | 6 | 32371299 | intron variant | A/G | snv | 0.35 | 2 | ||
| rs2469184 | 15 | 86648746 | intron variant | A/G | snv | 0.54 | 1 | ||||
| rs2228243 | 1.000 | 0.080 | 3 | 186677324 | missense variant | A/G;T | snv | 0.20; 4.0E-06 | 2 | ||
| rs1624230 | 3 | 186721146 | intron variant | C/A | snv | 0.42 | 1 | ||||
| rs1042445 | 3 | 186677647 | missense variant | C/A;T | snv | 0.27 | 1 | ||||
| rs7381103 | 5 | 177411311 | intron variant | C/G | snv | 0.11 | 1 | ||||
| rs7447593 | 5 | 177397136 | non coding transcript exon variant | C/G;T | snv | 2 | |||||
| rs2289252 | 1.000 | 0.040 | 4 | 186286227 | non coding transcript exon variant | C/T | snv | 0.35 | 2 | ||
| rs9898 | 0.925 | 0.160 | 3 | 186672838 | missense variant | C/T | snv | 0.38 | 0.43 | 2 | |
| rs3856930 | 3 | 186740533 | intron variant | C/T | snv | 0.27 | 1 | ||||
| rs5030028 | 3 | 186727965 | intron variant | C/T | snv | 0.23 | 1 | ||||
| rs12644950 | 4 | 154616169 | upstream gene variant | G/A | snv | 0.25 | 2 | ||||
| rs2304595 | 1.000 | 0.040 | 4 | 186251126 | non coding transcript exon variant | G/A | snv | 0.36 | 1 | ||
| rs5030023 | 3 | 186726855 | intron variant | G/A | snv | 0.20 | 1 | ||||
| rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 9 | |||
| rs17876032 | 5 | 177403626 | non coding transcript exon variant | G/A;C;T | snv | 0.52; 6.2E-04; 1.8E-04 | 1 | ||||
| rs4253304 | 4 | 186252417 | intron variant | G/C | snv | 0.36 | 1 | ||||
| rs16860992 | 1.000 | 0.080 | 3 | 186676249 | intron variant | G/C;T | snv | 2 | |||
| rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 11 | |||
| rs1593 | 4 | 186274397 | 3 prime UTR variant | T/A;G | snv | 3 |