Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs11234027 0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs12794714 0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs6742078 0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs7944926 0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2230808 0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140