Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61749715 | 0.851 | 0.120 | X | 154031154 | missense variant | G/A;C | snv | 8 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61749715 | 0.851 | 0.120 | X | 154031154 | missense variant | G/A;C | snv | 8 |