Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397514698 | 0.667 | 0.400 | 9 | 77797577 | missense variant | C/T | snv | 41 | |||
rs1331463984 | 0.701 | 0.240 | 16 | 2176350 | missense variant | G/A | snv | 33 |