Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121918494 | 0.790 | 0.160 | 10 | 121517363 | missense variant | G/C | snv | 24 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121918494 | 0.790 | 0.160 | 10 | 121517363 | missense variant | G/C | snv | 24 |