Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs5743618 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs5743810 0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs352139 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs1800451 0.776 0.240 10 52771466 missense variant C/T snv 3.2E-02 7.9E-02 9
rs3750920 0.807 0.120 11 1288726 synonymous variant C/T snv 0.40 0.38 7