Disease: Dermatitis, Atopic
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
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
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs555743307
IL4R
0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs569108
MS4A2
0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs11584340
FLG ; FLG-AS1
0.827 0.200 1 152313454 missense variant G/A snv 0.27 0.19 5
rs4982958 0.851 0.200 14 24518659 intergenic variant C/T snv 0.50 4
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 4
rs360721
IL18
0.882 0.200 11 112155193 intron variant G/A;C snv 3
rs438421
IL12RB1
0.882 0.200 19 18065276 intron variant A/G;T snv 3