Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs281875324 | 1.000 | 0.120 | 18 | 51065456 | missense variant | A/C;G | snv | 3 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs281875324 | 1.000 | 0.120 | 18 | 51065456 | missense variant | A/C;G | snv | 3 |