Disease: Allergic Reaction
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 3
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 3
rs7224129
GSDMB
0.925 0.160 17 39919173 non coding transcript exon variant G/A snv 0.52 3
rs7359623 0.925 0.160 17 39893336 intergenic variant C/T snv 0.44 3
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 3
rs8076131
ORMDL3
0.790 0.200 17 39924659 intron variant G/A;C snv 3
rs869402
GSDMB
0.925 0.160 17 39911790 intron variant T/A;C snv 3
rs907092
IKZF3
0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36 3
rs9901146 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 3
rs9907088 0.925 0.160 17 39878863 downstream gene variant G/A snv 0.39 3
rs9909593
IKZF3
0.925 0.160 17 39813896 intron variant A/G snv 0.38 3
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
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 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
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs13431828
IL1RL1 ; IL18R1
0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18 2
rs1362348
IL18R1
1.000 0.080 2 102368164 intron variant C/G snv 0.45 2