Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs4074 0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs5743314 0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs10433937 0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs1879026 1.000 0.080 4 186079167 intron variant G/C;T snv 3
rs111200466 1.000 0.080 4 153684312 5 prime UTR variant CGGCTGCTCGGCGTTCTCTCAGG/- delins 0.17 2
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs1281032650 5 96979168 missense variant A/G snv 1
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs762623 1.000 0.160 6 36677689 non coding transcript exon variant G/A snv 0.12 2
rs1325863623 6 2953175 missense variant C/T snv 4.0E-06 1
rs2071025 6 33175979 intron variant A/G snv 0.28 0.29 1
rs3116996 6 33130187 downstream gene variant T/A snv 0.13 1
rs61750420 0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 52
rs75961395 0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 10
rs1051861187 0.827 0.080 7 87409385 missense variant A/G snv 6
rs751703423 7 6023410 missense variant G/A;C snv 1
rs1420111973 1.000 0.080 9 117712527 synonymous variant T/C snv 7.0E-06 2
rs7096206 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs1316569885 10 95399139 missense variant C/T snv 4.0E-06 7.0E-06 1