| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1131692040 | 0.882 | 0.160 | X | 154399844 | missense variant | A/G | snv | 4 | |||
| rs727505397 | 0.882 | 0.240 | X | 41553782 | missense variant | C/T | snv | 3 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1131692040 | 0.882 | 0.160 | X | 154399844 | missense variant | A/G | snv | 4 | |||
| rs727505397 | 0.882 | 0.240 | X | 41553782 | missense variant | C/T | snv | 3 |