Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs749415085 | 0.807 | 0.160 | 3 | 179198937 | missense variant | C/A;G;T | snv | 7 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs749415085 | 0.807 | 0.160 | 3 | 179198937 | missense variant | C/A;G;T | snv | 7 |