Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121909092 | 0.882 | 0.120 | 19 | 10793829 | missense variant | G/A | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121909092 | 0.882 | 0.120 | 19 | 10793829 | missense variant | G/A | snv | 4 |