Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs35578035 | 17 | 33422168 | intron variant | T/C | snv | 0.53 | 1 | ||||
| rs4794977 | 17 | 33920566 | intron variant | C/G | snv | 0.49 | 1 | ||||
| rs3930349 | 17 | 33148527 | intron variant | C/A | snv | 0.22 | 1 | ||||
| rs73982435 | 17 | 33146437 | intron variant | C/A;T | snv | 1 |