Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913235 | 0.925 | 0.080 | 4 | 54727437 | missense variant | T/A;C;G | snv | 3 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913235 | 0.925 | 0.080 | 4 | 54727437 | missense variant | T/A;C;G | snv | 3 |