Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 5
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 4
rs12130333 1.000 0.080 1 62726106 regulatory region variant C/T snv 0.16 4
rs12425791 0.882 0.120 12 674318 downstream gene variant G/A;C snv 4
rs13143308 0.882 0.120 4 110793263 upstream gene variant T/C;G snv 4
rs7193788 0.925 0.120 16 82622555 upstream gene variant A/G snv 0.16 4
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 4
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 3
rs2005108 1.000 0.080 11 102899623 downstream gene variant C/G;T snv 3
rs6825454 1.000 0.080 4 154580036 downstream gene variant T/C snv 0.25 3
rs6843082 0.925 0.120 4 110796911 non coding transcript exon variant G/A snv 0.71 3
rs708495 0.925 0.120 14 52302622 intergenic variant T/A snv 0.57 3
rs75021220 0.882 0.120 4 110737238 intergenic variant C/A;T snv 3
rs11196288 1.000 0.080 10 113297684 regulatory region variant A/G snv 5.5E-02 2
rs11265260 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 2
rs12122341 1.000 0.080 1 115113069 regulatory region variant C/G snv 0.19 2
rs12445022 1.000 0.080 16 87541726 intergenic variant G/A snv 0.27 2
rs1341665 1.000 0.080 1 159721769 intergenic variant G/A snv 0.32 2
rs2020918 0.925 0.080 8 42214920 intergenic variant A/G snv 0.71 2
rs238670 1.000 0.080 20 23508073 intron variant T/G snv 3.9E-02 2
rs2589998 1.000 0.080 7 138181624 intergenic variant C/T snv 0.25 2
rs2592902 1.000 0.080 1 159685936 intergenic variant G/A;T snv 0.35 2
rs2801231 1.000 0.080 X 122083259 intergenic variant T/A;C;G snv 2
rs3917639 0.925 0.120 1 94527220 downstream gene variant C/T snv 2
rs4932370 1.000 0.080 15 90861475 intergenic variant G/A;C snv 2