Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121434594 | 0.827 | 0.160 | 3 | 12604189 | missense variant | G/A;C;T | snv | 5 | |||
rs397516830 | 0.827 | 0.160 | 3 | 12604182 | missense variant | A/C;G;T | snv | 5 | |||
rs80338796 | 0.667 | 0.480 | 3 | 12604200 | missense variant | G/A;C | snv | 4.0E-06 | 37 | ||
rs80338797 | 0.827 | 0.160 | 3 | 12584624 | missense variant | G/C;T | snv | 7 | |||
rs886039607 | 0.925 | 0.160 | 3 | 12608842 | missense variant | C/G | snv | 2 |