Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2151846 | 1.000 | 0.080 | 1 | 94122131 | upstream gene variant | T/G | snv | 0.41 | 1 | ||
| rs3789432 | 0.925 | 0.080 | 1 | 94109752 | intron variant | T/C | snv | 0.33 | 1 | ||
| rs3789451 | 1.000 | 0.080 | 1 | 94120772 | intron variant | C/G;T | snv | 1 | |||
| rs3789452 | 1.000 | 0.080 | 1 | 94121945 | upstream gene variant | T/A | snv | 0.26 | 1 | ||
| rs3827712 | 1.000 | 0.080 | 1 | 94109615 | intron variant | T/C;G | snv | 1 | |||
| rs4147811 | 1.000 | 0.080 | 1 | 94109500 | intron variant | C/T | snv | 0.33 | 1 | ||
| rs4147812 | 1.000 | 0.080 | 1 | 94109487 | intron variant | A/C;T | snv | 1 | |||
| rs4147816 | 1.000 | 0.080 | 1 | 94109224 | intron variant | C/T | snv | 0.33 | 1 | ||
| rs481931 | 0.882 | 0.120 | 1 | 94104460 | intron variant | G/T | snv | 0.32 | 1 | ||
| rs560426 | 0.851 | 0.200 | 1 | 94087882 | intron variant | C/T | snv | 0.53 | 1 | ||
| rs570926 | 1.000 | 0.080 | 1 | 94104662 | intron variant | T/C | snv | 0.39 | 1 | ||
| rs952499 | 1.000 | 0.080 | 1 | 94092869 | intron variant | T/C | snv | 0.45 | 1 |