Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17465637 | 0.790 | 0.200 | 1 | 222650187 | intron variant | A/C;G;T | snv | 0.64; 6.4E-06 | 3 | ||
| rs17465982 | 1.000 | 0.040 | 1 | 222664597 | intron variant | G/A | snv | 0.57 | 1 | ||
| rs2133189 | 0.925 | 0.040 | 1 | 222641100 | intron variant | C/T | snv | 0.56 | 1 | ||
| rs35158675 | 1.000 | 0.040 | 1 | 222656208 | intron variant | G/A;C | snv | 1 | |||
| rs67180937 | 1.000 | 0.040 | 1 | 222650401 | intron variant | T/C;G | snv | 0.64 | 1 |