Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750579 | 0.742 | 0.280 | 21 | 25891856 | missense variant | C/G;T | snv | 13 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750579 | 0.742 | 0.280 | 21 | 25891856 | missense variant | C/G;T | snv | 13 |