Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs745756308 | 1.000 | 2 | 138013874 | missense variant | T/C | snv | 4.0E-06 | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs745756308 | 1.000 | 2 | 138013874 | missense variant | T/C | snv | 4.0E-06 | 2 |