Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs759191907
LOC105379841 ; ENG
0.776 0.360 9 127825225 splice region variant A/G snv 8.0E-06 25
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs6894249
IRF1-AS1
0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45 9
rs569108
MS4A2
0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 6
rs2158177
TH2LCRR
0.925 0.120 5 132648366 intron variant A/G snv 0.18 5
rs2303067
SPINK5
0.851 0.160 5 148101392 missense variant A/G snv 0.52 0.44 5
rs9357733
EFHC1
0.851 0.160 6 52427338 intron variant A/G snv 0.19 4
rs13277355 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 3
rs13360927
TMEM232
0.882 0.160 5 110700055 intron variant A/G snv 9.3E-02 3
rs7518129
TNFSF4
0.882 0.120 1 173194429 intron variant A/G snv 0.47 3
rs11204971
FLG-AS1
0.925 0.120 1 152286602 intron variant A/G snv 0.15 2
rs112111458 0.925 0.120 2 70872975 intergenic variant A/G snv 0.16 2
rs17718511
SPINK5
0.925 0.120 5 148072009 intron variant A/G snv 3.2E-02 2
rs2066446
IL12RB2
0.925 0.120 1 67315434 intron variant A/G snv 0.20 2
rs28441202
RPTN ; PUDPP2
0.925 0.120 1 152156387 missense variant A/G snv 2
rs3756094
IRF2
0.925 0.120 4 184429780 intron variant A/G snv 0.66 2
rs4580194
GSDMA
1.000 0.040 17 39970224 intron variant A/G snv 0.41 2
rs5029949
TNFAIP3
0.925 0.120 6 137876369 intron variant A/G snv 8.1E-02 2
rs10468514 1.000 0.040 17 45378874 intergenic variant A/G snv 0.38 1