Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519913 | 0.925 | 0.120 | 1 | 11157172 | missense variant | G/C | snv | 3 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519913 | 0.925 | 0.120 | 1 | 11157172 | missense variant | G/C | snv | 3 |