Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912580 | 0.807 | 0.280 | 18 | 51067036 | missense variant | G/A;C;T | snv | 7 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912580 | 0.807 | 0.280 | 18 | 51067036 | missense variant | G/A;C;T | snv | 7 |