Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs886039469 | 0.701 | 0.560 | 10 | 76891709 | missense variant | T/C | snv | 35 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs886039469 | 0.701 | 0.560 | 10 | 76891709 | missense variant | T/C | snv | 35 |