Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 |