Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 175
rs6265 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 171
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs759834365 0.471 0.679 11 27658456 missense variant C/T snp 1.2E-05 157
rs1799945 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 152
rs4986790 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 146
rs1799983 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 138
rs11540654 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 117
rs1045642 0.520 0.714 7 87509329 synonymous variant A/G,T snp 0.50 0.56 108
rs1801133 0.533 0.714 1 11796321 missense variant G/A snp 0.31 0.26 86
rs2910164 0.525 0.750 5 160485411 mature miRNA variant C/G snp 0.71; 4.1E-06 0.71 82
rs4880 0.536 0.643 6 159692840 missense variant A/G snp 0.48 0.47 81
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 74
rs662 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 71
rs121913279 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 68
rs5443 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 65
rs671 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 61
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
rs854560 0.599 0.500 7 95316772 missense variant A/C,G,N,T snp 0.29 0.29 51
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 50
rs2234693 0.590 0.571 6 151842200 intron variant T/C snp 0.47 50
rs1800470 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 46
rs2070600 0.602 0.643 6 32183666 missense variant C/T snp 5.3E-02 4.4E-02 44
rs780094 0.699 0.286 2 27518370 intron variant T/C snp 0.67 44