Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs863224900 | 0.807 | 0.160 | 14 | 23428534 | missense variant | A/C;G;T | snv | 6 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs863224900 | 0.807 | 0.160 | 14 | 23428534 | missense variant | A/C;G;T | snv | 6 |