Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs782598150 | 1.000 | 0.160 | X | 101398021 | missense variant | C/A;G | snv | 5.5E-06 | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs782598150 | 1.000 | 0.160 | X | 101398021 | missense variant | C/A;G | snv | 5.5E-06 | 1 |