Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80356959 | 0.851 | 0.200 | 17 | 43045761 | missense variant | A/C;G | snv | 3 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80356959 | 0.851 | 0.200 | 17 | 43045761 | missense variant | A/C;G | snv | 3 |