Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398122887 | 0.790 | 0.280 | 19 | 41967744 | missense variant | C/G;T | snv | 5 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398122887 | 0.790 | 0.280 | 19 | 41967744 | missense variant | C/G;T | snv | 5 |