Disease: Allergic Reaction
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10173081
IL1RL1 ; IL18R1
1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs10192157
IL18R1 ; IL1RL1
1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 2
rs10206753
IL18R1 ; IL1RL1
1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 2
rs1043828
WDR36
1.000 0.080 5 111128310 3 prime UTR variant T/C;G snv 2
rs11078927
GSDMB
0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 2
rs11674302 1.000 0.080 2 102270668 intergenic variant T/C snv 0.16 2
rs11692065 1.000 0.080 2 102267515 intergenic variant C/T snv 0.15 2
rs13408569
IL1RL1 ; IL18R1
1.000 0.080 2 102338596 intron variant G/C snv 0.18 2
rs13408661
IL1RL1 ; IL18R1
1.000 0.080 2 102338622 intron variant G/A snv 0.18 2
rs1362348
IL18R1
1.000 0.080 2 102368164 intron variant C/G snv 0.45 2
rs17498196
LOC107987046 ; IL33
1.000 0.080 9 6237547 intron variant A/C;G snv 2
rs2066362
IL33
1.000 0.080 9 6219176 intron variant G/C;T snv 2
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 2
rs3771166
IL18R1
1.000 0.080 2 102369762 intron variant G/A;T snv 2
rs3771180
IL18R1 ; IL1RL1
1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 2
rs4795400
GSDMB
0.925 0.080 17 39910767 intron variant C/T snv 0.36 3
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 3
rs871657
IL1R1
1.000 0.080 2 102154881 intron variant C/T snv 0.22 2
rs907092
IKZF3
0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36 3
rs9303280
GSDMB
1.000 0.080 17 39917778 non coding transcript exon variant T/A;C snv 2
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 2
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs3755276
IL18R1
0.925 0.120 2 102361999 intron variant C/T snv 0.45 2
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 2