Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11084033 | 0.882 | 0.120 | 19 | 50850699 | intron variant | C/A;T | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11084033 | 0.882 | 0.120 | 19 | 50850699 | intron variant | C/A;T | snv | 4 |