Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1565868973 | 1.000 | 0.120 | 12 | 109796650 | missense variant | A/T | snv | 6 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1565868973 | 1.000 | 0.120 | 12 | 109796650 | missense variant | A/T | snv | 6 |