| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9313548 | 0.925 | 0.120 | 5 | 171534296 | TF binding site variant | C/T | snv | 0.56 | 1 | ||
| rs133885 | 1.000 | 0.120 | 22 | 25763322 | missense variant | G/A;C | snv | 0.55 | 1 | ||
| rs11855415 | 1.000 | 0.120 | 15 | 101334918 | intron variant | A/T | snv | 0.80 | 1 |