Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2296172 1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs340874 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 6
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs7570971 1.000 0.080 2 135080336 intron variant C/A snv 0.61 5
rs7578326 0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 3
rs7607980 1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 6
rs11709077 0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3
rs1470579 0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs1899951 0.851 0.160 3 12353341 intron variant C/T snv 0.26 2
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 4
rs2307111 0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs329122 1.000 0.080 5 134528909 intron variant G/A snv 0.45 2
rs4865796 1.000 0.080 5 53976834 intron variant G/A snv 0.72 3
rs2206734 0.882 0.160 6 20694653 intron variant C/T snv 0.20 4
rs2246012 1.000 0.080 6 131577068 intron variant T/A;C snv 2
rs35261542 1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs72892910 1.000 0.080 6 50849174 downstream gene variant G/T snv 0.17 2
rs9356744 0.882 0.120 6 20685255 intron variant T/C snv 0.42 5
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4