Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10187911 | 0.882 | 0.080 | 2 | 50420809 | intron variant | C/A;G;T | snv | 3 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10187911 | 0.882 | 0.080 | 2 | 50420809 | intron variant | C/A;G;T | snv | 3 |