Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267607002 | 1.000 | 0.040 | 10 | 110812303 | missense variant | C/A;T | snv | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267607002 | 1.000 | 0.040 | 10 | 110812303 | missense variant | C/A;T | snv | 2 |