Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267606985 | 1.000 | 12 | 27963693 | missense variant | A/G | snv | 3 | ||||
rs267606986 | 1.000 | 12 | 27963741 | missense variant | A/G | snv | 1 | ||||
rs267606987 | 1.000 | 12 | 27958559 | stop lost | T/C | snv | 1 | ||||
rs267606988 | 1.000 | 12 | 27963514 | stop gained | T/A | snv | 1 |