Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505922 0.724 0.357 None NA snp 0.37 24
rs760469299 0.821 0.071 17 12995005 T/A snp 4.0E-06 5
rs8176704 0.923 0.071 None NA snp 6.2E-02 4
rs117576373 0.923 0.071 17 48743314 C/T snp 2.5E-02 2
rs762529914
ERG
0.923 0.071 21 38383716 T/C snp 4.0E-06 2
rs775220785 0.923 0.071 7 99772615 C/T snp 8.0E-06 2
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 74
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 59
rs1800795 0.580 0.607 7 22727026 intron variant C/G snp 0.68 58
rs2736100 0.596 0.571 5 1286401 intron variant C/A snp 0.53 52
rs2234693 0.590 0.571 6 151842200 intron variant T/C snp 0.47 50
rs9340799 0.611 0.607 6 151842246 intron variant A/G snp 0.31 37
rs2279744 0.647 0.393 12 68808800 intron variant T/G snp 0.31 30
rs1501299 0.647 0.536 3 186853334 intron variant G/C,T snp 6.4E-05; 0.30 28
rs7975232
VDR
0.652 0.500 12 47845054 intron variant C/A snp 0.51 0.54 26
rs7679673 0.699 0.321 4 105140377 intron variant C/A snp 0.51 21
rs12255372 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 20
rs10505477 0.744 0.179 8 127395198 intron variant A/G snp 0.41 12
rs7501939 0.769 0.179 17 37741165 intron variant C/T snp 0.60 12
rs4430796 0.784 0.179 17 37738049 intron variant A/G snp 0.51 11
rs2298881 0.744 0.250 19 45423658 intron variant C/A,T snp 0.13 10
rs4988235 0.821 0.250 2 135851076 intron variant G/A,C snp 0.42 10
rs1447295 0.801 0.107 8 127472793 intron variant A/C,T snp 0.82; 3.2E-05 9
rs182052 0.801 0.250 3 186842993 intron variant G/A snp 0.39 9
rs2670660 0.769 0.286 17 5615686 intron variant A/G snp 0.41 8