Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12137855 0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 3
rs1420472625 0.925 0.040 19 54178800 missense variant G/C snv 2
rs2290602 0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs2294918 0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs4240624 0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
rs738491 0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs74315468 0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
rs2143571 0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs56225452 0.851 0.080 19 58513279 upstream gene variant C/T snv 0.18 5
rs2070666 0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs2645424 0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs2896019 0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs3480 0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs626283 0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs2854116 0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs1800234 0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42