Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67 22
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 13
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 10
rs1799945 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 8
rs2736100 0.596 0.571 5 1286401 intron variant C/A snp 0.53 7
rs3094054 0.821 0.214 6 30365728 intergenic variant G/A,T snp 2.7E-03; 7.8E-02 5
rs17817449
FTO
0.769 0.321 16 53779455 intron variant T/A,G snp 0.39 5
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 5
rs6265 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 4
rs10505477 0.744 0.179 8 127395198 intron variant A/G snp 0.41 4
rs9257809 0.801 0.286 6 29388554 intron variant A/G snp 6.3E-02 4
rs10069690 0.699 0.321 5 1279675 intron variant C/T snp 0.35 4
rs2046210 0.734 0.143 6 151627231 intergenic variant G/A snp 0.39 3
rs2363956 0.821 0.143 19 17283315 missense variant T/G snp 0.48 0.51 3
rs8170 0.801 0.143 19 17278895 synonymous variant G/A snp 0.15 0.19 3
rs6983267 0.667 0.214 8 127401060 non coding transcript exon variant G/T snp 0.38 3
rs4810485 0.784 0.321 20 46119308 intron variant T/A,G snp 0.79 3
rs10811650 0.878 0.143 9 22067594 intron variant A/G snp 0.37 3
rs6025
F5
0.756 0.250 1 169549811 missense variant C/T snp 0.98 0.98 3
rs1801131 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 3
rs1801133 0.533 0.714 1 11796321 missense variant G/A snp 0.31 0.26 3
rs1053872 0.923 0.071 9 4860643 3 prime UTR variant G/C,T snp 0.31 3
rs1154865 1.000 0.071 12 73596057 intergenic variant C/G snp 0.22 2
rs16886165 0.923 0.071 5 56727256 intergenic variant T/G snp 0.22 2
rs2494251 0.923 0.071 1 159311361 intergenic variant G/A,C snp 0.35 2