Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs77316810 | 0.776 | 0.200 | 10 | 43113654 | missense variant | T/A;C;G | snv | 10 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs77316810 | 0.776 | 0.200 | 10 | 43113654 | missense variant | T/A;C;G | snv | 10 |