Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587782177 | 0.763 | 0.200 | 17 | 7674887 | missense variant | C/A;G;T | snv | 11 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587782177 | 0.763 | 0.200 | 17 | 7674887 | missense variant | C/A;G;T | snv | 11 |