Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs29001566 | 0.807 | 0.080 | 3 | 129533711 | missense variant | C/A;G;T | snv | 10 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs29001566 | 0.807 | 0.080 | 3 | 129533711 | missense variant | C/A;G;T | snv | 10 |