Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10090787 | 1.000 | 0.080 | 8 | 120798309 | intron variant | C/T | snv | 0.34 | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10090787 | 1.000 | 0.080 | 8 | 120798309 | intron variant | C/T | snv | 0.34 | 2 |