Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10889676 | 0.827 | 0.120 | 1 | 67256884 | intron variant | C/A;T | snv | 5 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10889676 | 0.827 | 0.120 | 1 | 67256884 | intron variant | C/A;T | snv | 5 |