Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs57077886 | 0.776 | 0.240 | 1 | 156114947 | missense variant | C/T | snv | 9 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs57077886 | 0.776 | 0.240 | 1 | 156114947 | missense variant | C/T | snv | 9 |