Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28929485 | 0.807 | 0.320 | 13 | 20189532 | missense variant | G/A;C | snv | 7 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28929485 | 0.807 | 0.320 | 13 | 20189532 | missense variant | G/A;C | snv | 7 |