Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234694 0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02 3
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs281432 0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs11651270 0.882 0.240 17 5521757 missense variant T/C snv 0.45 0.47 4
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs61758388 0.851 0.360 16 17470454 missense variant C/A;G snv 2.7E-02 4
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs10770125 0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
rs1326934 0.925 0.200 10 95524324 intron variant C/T snv 0.63 2
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157