Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs539699299 | 0.851 | 0.160 | 7 | 107661725 | missense variant | C/A;G | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs539699299 | 0.851 | 0.160 | 7 | 107661725 | missense variant | C/A;G | snv | 4 |