Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs116577908 | 3 | 17056907 | intron variant | A/G | snv | 7.1E-03 | 4 | ||||
| rs73146904 | 3 | 16891490 | intron variant | G/A | snv | 9.4E-02 | 3 | ||||
| rs1992381 | 3 | 16886567 | intron variant | T/A;C | snv | 1 | |||||
| rs144614991 | 3 | 16925189 | intron variant | C/T | snv | 3.9E-02 | 1 |