Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10954213 0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs10954214 0.851 0.160 7 128949579 3 prime UTR variant C/T snv 0.64 4
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs2280714 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs12531711 0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs13238352 0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 5
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs5029924 0.851 0.200 6 137866361 intron variant C/T snv 0.13 4
rs5029937 0.882 0.160 6 137874014 intron variant G/T snv 0.13 4
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs77191406 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 4
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4958880 0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 5
rs4112788 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 4
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs3027898 0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs1059702 0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65