| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894927 | 0.882 | 0.080 | X | 46853731 | stop gained | C/T | snv | 4 | |||
| rs62642057 | 0.882 | 0.080 | X | 38304746 | missense variant | C/T | snv | 3 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894927 | 0.882 | 0.080 | X | 46853731 | stop gained | C/T | snv | 4 | |||
| rs62642057 | 0.882 | 0.080 | X | 38304746 | missense variant | C/T | snv | 3 |