Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs879255280 | 0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv | 22 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs879255280 | 0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv | 22 |