Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113994087 | 0.827 | 0.120 | 2 | 29209798 | missense variant | C/A;T | snv | 8 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113994087 | 0.827 | 0.120 | 2 | 29209798 | missense variant | C/A;T | snv | 8 |