| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913506 | 0.677 | 0.320 | 4 | 54733154 | missense variant | G/A;C;T | snv | 24 | |||
| rs1057519710 | 0.695 | 0.280 | 4 | 54733166 | missense variant | G/C;T | snv | 22 | |||
| rs755383 | 0.807 | 0.120 | 9 | 863635 | intron variant | C/T | snv | 0.54 | 7 |