Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398124146 | 0.742 | 0.360 | 16 | 3738617 | missense variant | G/A;C | snv | 12 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398124146 | 0.742 | 0.360 | 16 | 3738617 | missense variant | G/A;C | snv | 12 |