| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1557036768 | 0.708 | 0.320 | X | 53647390 | missense variant | C/T | snv | 44 | |||
| rs1325394060 | 0.851 | 0.320 | X | 53534144 | missense variant | C/G;T | snv | 9.5E-06 | 9 | ||
| rs1556978515 | 0.851 | 0.280 | X | 53591113 | missense variant | T/C | snv | 7 |