Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs122460159 | 0.807 | 0.200 | X | 18564496 | missense variant | C/T | snv | 6 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs122460159 | 0.807 | 0.200 | X | 18564496 | missense variant | C/T | snv | 6 |