Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519997 | 0.776 | 0.320 | 17 | 7676037 | missense variant | A/C;G;T | snv | 9 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519997 | 0.776 | 0.320 | 17 | 7676037 | missense variant | A/C;G;T | snv | 9 |