Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519753 0.763 0.120 1 64846664 missense variant C/A snv 9
rs10740055 0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913488 0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs775144154 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs121913502 0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs387906659 0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs2293157 0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs2308950 0.882 0.040 1 15507011 missense variant C/G;T snv 4.0E-06; 1.1E-02 3
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs121913459 0.672 0.160 9 130872896 missense variant C/T snv 25
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs2285053 0.752 0.320 16 55478465 intron variant C/T snv 0.12 15
rs2075686 0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02 13
rs10821936 0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs7727691 0.763 0.200 5 83075876 intron variant C/T snv 0.32 9