Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267606670 | 0.790 | 0.320 | 19 | 41968837 | missense variant | C/A;T | snv | 17 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267606670 | 0.790 | 0.320 | 19 | 41968837 | missense variant | C/A;T | snv | 17 |