Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398123317 | 0.790 | 0.160 | 10 | 87925550 | missense variant | T/A;C;G | snv | 8 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398123317 | 0.790 | 0.160 | 10 | 87925550 | missense variant | T/A;C;G | snv | 8 |