Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3130215 | 0.882 | 0.240 | 6 | 33107186 | intron variant | A/G | snv | 0.69 | 3 | ||
rs2064478 | 0.925 | 0.200 | 6 | 33104489 | intron variant | C/T | snv | 0.28 | 2 | ||
rs2064476 | 0.925 | 0.200 | 6 | 33105545 | intron variant | A/G | snv | 0.37 | 2 | ||
rs4282438 | 0.807 | 0.280 | 6 | 33104395 | intron variant | T/G | snv | 3.1E-02 | 2 | ||
rs3117231 | 1.000 | 0.120 | 6 | 33107131 | intron variant | A/G | snv | 0.31 | 1 | ||
rs3128927 | 1.000 | 0.120 | 6 | 33106511 | intron variant | C/G;T | snv | 1 |