| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4911198 | 0.925 | 0.040 | 20 | 32139880 | intron variant | C/A;T | snv | 2 | |||
| rs6142618 | 20 | 32137845 | intron variant | A/G | snv | 0.69 | 1 | ||||
| rs6058526 | 1.000 | 0.040 | 20 | 32111829 | intron variant | A/G | snv | 0.14 | 1 | ||
| rs17093831 | 20 | 32111119 | intron variant | T/C | snv | 2.6E-02 | 1 |