Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10033825 | 0.925 | 0.120 | 4 | 10495168 | intron variant | C/T | snv | 0.28 | 3 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10033825 | 0.925 | 0.120 | 4 | 10495168 | intron variant | C/T | snv | 0.28 | 3 |