Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10485505 | 1.000 | 0.080 | 20 | 34437762 | intron variant | C/G;T | snv | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10485505 | 1.000 | 0.080 | 20 | 34437762 | intron variant | C/G;T | snv | 2 |