Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587782529 | 0.851 | 0.200 | 17 | 7670700 | missense variant | G/A;C | snv | 3 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587782529 | 0.851 | 0.200 | 17 | 7670700 | missense variant | G/A;C | snv | 3 |