Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519043 | 0.851 | 0.120 | 10 | 121517391 | missense variant | C/A;G;T | snv | 3 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519043 | 0.851 | 0.120 | 10 | 121517391 | missense variant | C/A;G;T | snv | 3 |