Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519728 | 0.851 | 0.120 | 15 | 66435103 | missense variant | T/A;C;G | snv | 5 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519728 | 0.851 | 0.120 | 15 | 66435103 | missense variant | T/A;C;G | snv | 5 |