Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
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
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs2243248
IL4
0.763 0.240 5 132672952 upstream gene variant T/A;C;G snv 9
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs11747270 0.790 0.240 5 150879305 intron variant A/G snv 0.21 7
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs1027009063 0.925 0.040 2 8802974 stop gained G/A snv 2
rs3811463 0.752 0.400 1 26427451 3 prime UTR variant T/A;C snv 14
rs2521634 0.882 0.040 7 24338421 intron variant G/A;C snv 3
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47