| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057518960 | 0.882 | 0.160 | 6 | 121447333 | missense variant | G/C | snv | 7 | |||
| rs1556009247 | 0.882 | X | 72490973 | missense variant | A/C;T | snv | 7 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057518960 | 0.882 | 0.160 | 6 | 121447333 | missense variant | G/C | snv | 7 | |||
| rs1556009247 | 0.882 | X | 72490973 | missense variant | A/C;T | snv | 7 |