Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16948627 | 0.882 | 0.040 | 17 | 50063432 | intron variant | C/A;T | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16948627 | 0.882 | 0.040 | 17 | 50063432 | intron variant | C/A;T | snv | 4 |