Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17824933 | 1.000 | 0.080 | 11 | 60993140 | intron variant | C/A;G | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17824933 | 1.000 | 0.080 | 11 | 60993140 | intron variant | C/A;G | snv | 1 |