Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10873876 | 1.000 | 0.040 | 1 | 76306643 | intron variant | T/C | snv | 0.75 | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10873876 | 1.000 | 0.040 | 1 | 76306643 | intron variant | T/C | snv | 0.75 | 1 |