Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs3130380 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs9261290 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs3099844 0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs12198173 0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs2247056 0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs13199524 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 8