Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs316019 0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs75444904 0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 4
rs841853 0.882 0.200 1 42935767 intron variant A/C snv 0.66 4
rs2120243 0.925 0.200 3 157429779 intron variant A/C snv 0.59 3
rs2234694 0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02 3
rs9942471 0.925 0.160 6 89238513 intergenic variant A/C snv 0.37 2
rs1866813 1.000 0.120 3 137083096 intergenic variant A/C snv 0.14 1
rs304029 1.000 0.120 3 4504140 intron variant A/C snv 0.35 1
rs953239 1.000 0.120 3 142727363 intron variant A/C snv 0.46 1
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1252906 1.000 0.120 14 59192073 intron variant A/C;G snv 1
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70