Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4240624 0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2294918 0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs626283 0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs3480 0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs2645424 0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs2854116 0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs738491 0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs2143571 0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs2896019 0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs12137855 0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 3
rs56225452 0.851 0.080 19 58513279 upstream gene variant C/T snv 0.18 5
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42