Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104886028 | 1.000 | 0.080 | 12 | 25227308 | missense variant | C/T | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104886028 | 1.000 | 0.080 | 12 | 25227308 | missense variant | C/T | snv | 1 |