Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397507531 | 0.752 | 0.320 | 12 | 112473040 | missense variant | T/C;G | snv | 18 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397507531 | 0.752 | 0.320 | 12 | 112473040 | missense variant | T/C;G | snv | 18 |