Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
rs16139 0.657 0.500 7 24285260 missense variant T/A,C snp 4.0E-06; 3.0E-02 3.2E-02 27
rs1800796 0.647 0.571 7 22726627 non coding transcript exon variant G/C snp 0.10 26
rs237025 0.679 0.357 6 149400554 missense variant G/A snp 0.55 0.57 20
rs4402960 0.756 0.286 3 185793899 intron variant G/T snp 0.38 12
rs10811661 0.846 0.214 9 22134095 intergenic variant T/C snp 0.14 8
rs1800764 0.801 0.250 17 63473168 intergenic variant C/G,T snp 0.45 8
rs61758388 0.784 0.321 16 17470454 missense variant C/A,G snp 2.7E-02 1.6E-02 7
rs713041 0.821 0.286 19 1106616 stop gained T/A,C snp 4.2E-06; 0.58 0.61 7
rs281432 0.821 0.250 19 10279982 intron variant C/G snp 0.51 6
rs759853 0.821 0.286 7 134459206 non coding transcript exon variant G/A snp 0.33 5
rs316019 0.878 0.179 6 160249250 missense variant A/C snp 0.90 0.89 4
rs1326934 0.878 0.250 10 95524324 intron variant C/T snp 0.64 3
rs1567438 0.923 0.179 6 160458599 intron variant T/C snp 0.26 3
rs10770125 0.923 0.179 11 2147784 missense variant A/G snp 0.49 0.41 2
rs2457576 0.923 0.179 6 160444587 intron variant G/C snp 0.28 2
rs3820589 0.923 0.179 1 42960373 intron variant A/T snp 7.8E-02 2