Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13222905 0.882 0.160 7 150566901 upstream gene variant G/A snv 0.15 3
rs6965571 0.882 0.160 7 150737384 5 prime UTR variant G/A snv 0.18 3
rs2290400 0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs3117098 0.851 0.280 6 32390736 non coding transcript exon variant G/A snv 0.72 4
rs3134792 0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 4
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs9273349 0.827 0.200 6 32658092 upstream gene variant T/C;G snv 6
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
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
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs61839660 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1805011 0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 8
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs4505848 0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1701704 0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9