Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1883025 0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs3890182 0.925 0.120 9 104885374 intron variant G/A;T snv 4
rs4149268 1.000 0.040 9 104884939 intron variant C/T snv 0.46 4
rs2515629 1.000 0.040 9 104832083 intron variant A/G snv 0.16 3
rs3905000 0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 2
rs2066718 0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 2
rs9282541 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2