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
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs4680 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 155
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
rs25487 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 119
rs11540654 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 117
rs1695 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 100
rs1799782 0.523 0.607 19 43553422 stop gained G/A snp 9.5E-02 7.1E-02 84
rs13181 0.525 0.536 19 45351661 stop gained T/A,G snp 4.0E-06; 0.32 0.32 82
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
rs1052133 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 77
rs1801282 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 77
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
rs1805192 0.545 0.679 3 12379739 missense variant C/G snp 75
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
rs1800629
TNF
0.549 0.786 6 31575254 intergenic variant G/A snp 0.12 0.15 69
rs5443 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 65
rs861539 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 60
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
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 56