Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs58072617 | 0.790 | 0.120 | 12 | 52517702 | missense variant | A/G;T | snv | 7 | |||
rs61027685 | 0.882 | 0.080 | 17 | 41586438 | missense variant | C/A;G;T | snv | 3 | |||
rs61222761 | 0.925 | 0.080 | 12 | 52519824 | missense variant | T/A | snv | 2 | |||
rs61263401 | 0.925 | 0.080 | 17 | 41586480 | missense variant | T/C | snv | 2 |