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
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
rs4986791 0.501 0.714 9 117713324 missense variant C/T snp 5.7E-02 5.1E-02 108
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
rs1801282 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 77
rs1805192 0.545 0.679 3 12379739 missense variant C/G snp 75
rs5443 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 65
rs1800795 0.580 0.607 7 22727026 intron variant C/G snp 0.68 58
rs5498 0.570 0.679 19 10285007 missense variant A/G snp 0.44 0.36 53
rs4420638 0.724 0.321 19 44919689 intergenic variant A/G snp 0.19 32
rs6280 0.652 0.357 3 114171968 missense variant C/T snp 0.63 0.56 31
rs11549465 0.662 0.357 14 61740839 missense variant C/T snp 8.8E-02 7.0E-02 27
rs16139 0.657 0.500 7 24285260 missense variant T/A,C snp 4.0E-06; 3.0E-02 3.2E-02 27
rs1049353 0.657 0.464 6 88143916 synonymous variant C/T snp 0.21 0.20 26
rs1800796 0.647 0.571 7 22726627 non coding transcript exon variant G/C snp 0.10 26
rs696217 0.685 0.536 3 10289773 missense variant G/T snp 8.8E-02 7.2E-02 24
rs2241766 0.679 0.393 3 186853103 synonymous variant T/C,G snp 8.0E-06; 0.13 9.0E-02 23
rs11887534 0.685 0.357 2 43839108 missense variant G/A,C snp 6.4E-06; 6.7E-02 6.4E-02 20
rs237025 0.679 0.357 6 149400554 missense variant G/A snp 0.55 0.57 20
rs80356814 0.724 0.321 1 156138697 synonymous variant C/T snp 8.0E-06 3.2E-05 16
rs14259 0.734 0.321 12 121915890 missense variant A/C,G snp 4.0E-06; 0.32 0.26 15