Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17498196 | 1.000 | 0.080 | 9 | 6237547 | intron variant | A/C;G | snv | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17498196 | 1.000 | 0.080 | 9 | 6237547 | intron variant | A/C;G | snv | 2 |