Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587781525 | 0.689 | 0.480 | 17 | 7673778 | missense variant | T/A;C;G | snv | 20 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587781525 | 0.689 | 0.480 | 17 | 7673778 | missense variant | T/A;C;G | snv | 20 |