| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121434612 | 1.000 | 0.080 | X | 111142119 | missense variant | C/T | snv | 1 | |||
| rs121434613 | 0.882 | 0.240 | X | 111194402 | missense variant | C/A | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121434612 | 1.000 | 0.080 | X | 111142119 | missense variant | C/T | snv | 1 | |||
| rs121434613 | 0.882 | 0.240 | X | 111194402 | missense variant | C/A | snv | 1 |