Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs193922613 | 0.925 | 0.160 | 3 | 10149847 | missense variant | A/G;T | snv | 3 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs193922613 | 0.925 | 0.160 | 3 | 10149847 | missense variant | A/G;T | snv | 3 |