| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
| rs821577 | 0.882 | 0.160 | 1 | 231931311 | intron variant | T/C;G | snv | 3 | |||
| rs1538979 | 0.882 | 0.160 | 1 | 231761122 | intron variant | C/T | snv | 0.19 | 3 | ||
| rs821633 | 0.882 | 0.160 | 1 | 232013187 | intron variant | T/C | snv | 0.37 | 3 |