Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397508272 | 1.000 | 0.120 | 7 | 117509038 | missense variant | T/C;G | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397508272 | 1.000 | 0.120 | 7 | 117509038 | missense variant | T/C;G | snv | 1 |