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
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
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
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs2395029 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12