Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs73146904 | 3 | 16891490 | intron variant | G/A | snv | 9.4E-02 | 3 | ||||
| rs9821630 | 3 | 16929446 | intron variant | A/G | snv | 0.24 | 2 | ||||
| rs200726463 | 3 | 16992491 | intron variant | -/AG | delins | 7.1E-03 | 1 | ||||
| rs79638618 | 3 | 16890061 | intron variant | C/T | snv | 3.7E-02 | 1 |