Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs7096206 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs56061981 0.851 0.120 4 76023632 intron variant C/T snv 7.6E-02 5
rs4842407 0.882 0.200 12 78807293 intron variant A/G snv 0.35 4
rs11012476 0.925 0.120 10 21003994 intron variant C/T snv 3.5E-02 3
rs201565523 0.925 0.240 2 218390027 missense variant C/T snv 2.9E-04 7.7E-05 3