Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10739221 | 0.851 | 0.080 | 9 | 106298549 | intron variant | T/C;G | snv | 5 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10739221 | 0.851 | 0.080 | 9 | 106298549 | intron variant | T/C;G | snv | 5 |