Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750306 | 0.701 | 0.320 | 14 | 73173663 | missense variant | A/C;G;T | snv | 16 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750306 | 0.701 | 0.320 | 14 | 73173663 | missense variant | A/C;G;T | snv | 16 |