| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111033632 | 0.925 | 0.120 | 1 | 119967555 | missense variant | C/T | snv | 2 | |||
| rs312262798 | 0.925 | 0.120 | 1 | 119917763 | splice acceptor variant | C/T | snv | 2 | |||
| rs1557804111 | 1.000 | 0.120 | 1 | 119920277 | stop gained | G/A | snv | 1 |