Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057518950 | 0.851 | 0.280 | 2 | 1484815 | missense variant | C/T | snv | 7 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057518950 | 0.851 | 0.280 | 2 | 1484815 | missense variant | C/T | snv | 7 |