| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs80356537 | 0.752 | 0.320 | 19 | 41970405 | missense variant | C/A;G;T | snv | 17 | |||
| rs387907281 | 0.752 | 0.280 | 19 | 41970284 | missense variant | C/T | snv | 13 | |||
| rs879255368 | 19 | 41984953 | missense variant | C/G;T | snv | 5 |