Source: UNIPROT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs67120076 | 1.000 | 0.120 | X | 38408752 | missense variant | C/G;T | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs67120076 | 1.000 | 0.120 | X | 38408752 | missense variant | C/G;T | snv | 1 |