Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 23
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 22
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 18
rs1789924 0.821 0.143 4 99353129 intergenic variant C/G,T snp 0.34 8
rs3782886 0.784 0.250 12 111672685 synonymous variant T/C snp 1.9E-02 1.4E-02 8
rs111576572 0.878 0.071 21 37617262 A/G snp 0.31 5
rs2835831 0.878 0.071 21 37614931 3 prime UTR variant T/C snp 0.30 5
rs2835833 0.878 0.071 21 37615595 3 prime UTR variant G/A snp 0.32 5
rs2835835 0.878 0.071 21 37616770 G/A snp 0.32 5
rs2835836 0.878 0.071 21 37616885 A/C snp 0.27 5
rs2835837 0.878 0.071 21 37618141 3 prime UTR variant G/A snp 0.30 5
rs2835838 0.878 0.071 21 37618692 3 prime UTR variant A/G snp 0.32 5
rs2835839 0.878 0.071 21 37618732 3 prime UTR variant T/C snp 0.26 5
rs2835840 0.878 0.071 21 37619019 3 prime UTR variant G/C snp 0.30 5
rs4816567 0.878 0.071 21 37615853 3 prime UTR variant T/C snp 0.32 5
rs4816568 0.878 0.071 21 37616044 3 prime UTR variant A/G,T snp 0.31 5
rs4817877 0.878 0.071 21 37616091 3 prime UTR variant G/C snp 0.32 5
rs702858 0.878 0.071 21 37622867 3 prime UTR variant A/G snp 0.72 5
rs73220488 0.878 0.071 21 37614723 3 prime UTR variant C/T snp 0.25; 8.2E-05 5
rs73220491 0.878 0.071 21 37616021 3 prime UTR variant T/G snp 0.31 5
rs73220494 0.878 0.071 21 37616974 3 prime UTR variant C/T snp 0.31 5
rs73220495 0.878 0.071 21 37617410 3 prime UTR variant G/A snp 0.30 5
rs75938265 0.878 0.071 21 37614737 snp 0.31 5
rs857980 0.878 0.071 21 37622840 3 prime UTR variant G/A snp 0.72 5
rs6265 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 5