Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80338758 | 0.790 | 0.400 | X | 71127367 | missense variant | C/A;T | snv | 9 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80338758 | 0.790 | 0.400 | X | 71127367 | missense variant | C/A;T | snv | 9 |