Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs199472833 | 1.000 | 0.120 | 7 | 150974926 | missense variant | A/C;G;T | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs199472833 | 1.000 | 0.120 | 7 | 150974926 | missense variant | A/C;G;T | snv | 1 |