Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs138707712 | 1.000 | 0.040 | 1 | 36447523 | intron variant | T/C | snv | 1.1E-02 | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs138707712 | 1.000 | 0.040 | 1 | 36447523 | intron variant | T/C | snv | 1.1E-02 | 1 |