Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs63750447 0.716 0.200 3 37025749 missense variant T/A snv 2.7E-03 7.5E-04 17
rs140693 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 10
rs386656364 0.807 0.160 2 233682328 missense variant CG/AA mnv 8
rs1131341 0.925 0.160 16 69714966 missense variant G/A;C snv 3.2E-02 2.6E-02 4
rs587778964 0.882 0.160 3 37048604 missense variant A/C;T snv 4
rs17224367 0.882 0.160 2 47429833 missense variant C/G;T snv 1.5E-03 3
rs63750070 0.882 0.160 2 47410245 missense variant T/C;G snv 3
rs17868323 0.925 0.160 2 233682324 missense variant T/A;G snv 0.59 2
rs63750228 1.000 0.080 2 47429926 missense variant C/A;G snv 4.0E-06 1
rs876661188 1.000 0.080 3 37050573 missense variant C/T snv 1
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs2839698 0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25
rs2043556 0.716 0.440 10 51299646 non coding transcript exon variant T/C snv 0.25 0.24 17
rs4135385 0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105