Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs3021097 0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs770460061 0.742 0.240 11 67585239 missense variant T/C;G snv 4.0E-06; 1.2E-05 14
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs758244932 0.827 0.120 1 225828842 missense variant C/T snv 1.3E-04 1.0E-04 5