| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs132630304 | 0.882 | 0.080 | X | 150598660 | missense variant | C/G;T | snv | 3 | |||
| rs587783752 | 0.925 | 0.080 | X | 150657854 | frameshift variant | AA/-;AAA | delins | 2 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs132630304 | 0.882 | 0.080 | X | 150598660 | missense variant | C/G;T | snv | 3 | |||
| rs587783752 | 0.925 | 0.080 | X | 150657854 | frameshift variant | AA/-;AAA | delins | 2 |