Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397507514 | 0.790 | 0.240 | 12 | 112450408 | missense variant | G/C;T | snv | 9 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397507514 | 0.790 | 0.240 | 12 | 112450408 | missense variant | G/C;T | snv | 9 |