Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17301608 | 0.925 | 0.080 | 16 | 55484698 | intron variant | C/A;G;T | snv | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17301608 | 0.925 | 0.080 | 16 | 55484698 | intron variant | C/A;G;T | snv | 2 |