Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs730882025 | 0.724 | 0.360 | 17 | 7674885 | missense variant | C/A;G;T | snv | 21 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs730882025 | 0.724 | 0.360 | 17 | 7674885 | missense variant | C/A;G;T | snv | 21 |