Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913492 | 0.790 | 0.160 | 9 | 77794572 | missense variant | T/A;C;G | snv | 11 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913492 | 0.790 | 0.160 | 9 | 77794572 | missense variant | T/A;C;G | snv | 11 |