Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12601991 | 0.708 | 0.280 | 17 | 37741642 | intron variant | T/A;G | snv | 17 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12601991 | 0.708 | 0.280 | 17 | 37741642 | intron variant | T/A;G | snv | 17 |