| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs755991142 | 1.000 | 0.080 | X | 109475908 | missense variant | C/G;T | snv | 1.1E-05 | 1 | ||
| rs779221554 | 1.000 | 0.040 | X | 109430395 | missense variant | C/A;T | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs755991142 | 1.000 | 0.080 | X | 109475908 | missense variant | C/G;T | snv | 1.1E-05 | 1 | ||
| rs779221554 | 1.000 | 0.040 | X | 109430395 | missense variant | C/A;T | snv | 1 |