Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2070666 0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs2143571 0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs2290602 0.882 0.040 4 23824109 intron variant T/A;G snv 3
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
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
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1420472625 0.925 0.040 19 54178800 missense variant G/C snv 2
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800234 0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs2294918 0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42