| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs281874674 | 0.827 | 0.280 | X | 108597479 | missense variant | G/C;T | snv | 8 | |||
| rs1175052474 | 1.000 | 2 | 227295295 | inframe insertion | -/AGG | delins | 7.0E-06 | 5 | |||
| rs1569492161 | 0.882 | 0.280 | X | 108586729 | missense variant | G/C | snv | 4 | |||
| rs1556446493 | X | 108668328 | missense variant | G/T | snv | 3 |