Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893856 | 0.827 | 0.080 | 4 | 41746162 | missense variant | C/T | snv | 6 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893856 | 0.827 | 0.080 | 4 | 41746162 | missense variant | C/T | snv | 6 |