Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894201 | 0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv | 12 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894201 | 0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv | 12 |