Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs527236119 | 0.925 | 0.200 | 1 | 215782779 | missense variant | T/C;G | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs527236119 | 0.925 | 0.200 | 1 | 215782779 | missense variant | T/C;G | snv | 1 |