IL33, interleukin 33, 90865

N. diseases: 487; N. variants: 29
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs928413
rs928413
Entrez Id: 90865
Gene Symbol: IL33
IL33
CUI: C0741260
Disease:
Adult onset asthma
G 0.700 GeneticVariation GWASCAT Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. 31036433 2019
dbSNP: rs928413
rs928413
Entrez Id: 90865
Gene Symbol: IL33
IL33
CUI: C0155877
Disease:
Allergic asthma
0.010 GeneticVariation BEFREE This study aimed to investigate whether the genetic polymorphisms of CDHR3 (rs6967330), GSDMB (rs2305480), IL33 rs928413, RAD50 (rs6871536) and IL1RL1 (rs1558641) are associated with the development of atopic asthma in Chinese population. 26493291 2015
dbSNP: rs12339348
rs12339348
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C1527304
Disease:
Allergic Reaction
T 0.800 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs12339348
rs12339348
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C1527304
Disease:
Allergic Reaction
0.800 GeneticVariation GWASCAT A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. 29785011 2018
dbSNP: rs10815393
rs10815393
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C1527304
Disease:
Allergic Reaction
C 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs10975488
rs10975488
Entrez Id: 90865
Gene Symbol: IL33
IL33
CUI: C1527304
Disease:
Allergic Reaction
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs10975507
rs10975507
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C1527304
Disease:
Allergic Reaction
T 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs17498196
rs17498196
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C1527304
Disease:
Allergic Reaction
C 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs17582919
rs17582919
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C1527304
Disease:
Allergic Reaction
C 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs2066362
rs2066362
Entrez Id: 90865
Gene Symbol: IL33
IL33
CUI: C1527304
Disease:
Allergic Reaction
T 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs7019575
rs7019575
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C1527304
Disease:
Allergic Reaction
C 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs7848215
rs7848215
Entrez Id: 90865
Gene Symbol: IL33
IL33
CUI: C1527304
Disease:
Allergic Reaction
T 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs928413
rs928413
Entrez Id: 90865
Gene Symbol: IL33
IL33
CUI: C1527304
Disease:
Allergic Reaction
G 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs4742170
rs4742170
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C3662483
Disease:
Allergic sensitization
0.010 GeneticVariation BEFREE This mechanism may explain the negative effect of the rs4742170 (T) risk allele on the development of wheezing phenotype that strongly correlates with allergic sensitization in childhood. 30544846 2018
dbSNP: rs11792633
rs11792633
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C0494463
Disease:
Alzheimer Disease, Late Onset
0.010 GeneticVariation BEFREE The results showed that IL-33 rs11792633 polymorphism had statistically significant correlation with a decreased risk of LOAD in heterozygous comparison model (OR =0.64, 95% CI =0.48-0.83), homozygote comparison model (OR =0.83, 95% CI =0.74-0.93), dominant model (OR =0.78, 95% CI =0.67-0.91), recessive model (OR =0.70, 95% CI =0.59-0.84), and allelic model (OR =0.79, 95% CI =0.69-0.91), which were also validated by stratified subgroup analysis. 28919759 2017
dbSNP: rs7044343
rs7044343
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C0494463
Disease:
Alzheimer Disease, Late Onset
0.010 GeneticVariation BEFREE Additionally, there was an apparent association between the IL-33 rs7044343 variant and LOAD ri</span>sk under four genetic models for overall population (heterozygous comparison model: OR =0.75, 95% CI =0.63-0.89; dominant model: OR =0.83, 95% CI =0.70-0.98; recessive model: OR =0.80, 95% CI =0.68-0.94; allelic model: OR =0.86, 95% CI =0.79-0.94) as well as Caucasian subgroup. 28919759 2017
dbSNP: rs11792633
rs11792633
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE Three intronic rs1157505, rs11792633, and rs7044343 single nucleotide polymorphisms (SNPs) within IL-33 have recently been reported to be associated with risk of AD in Caucasian populations. 20708824 2012
dbSNP: rs7044343
rs7044343
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE Three intronic rs1157505, rs11792633, and rs7044343 single nucleotide polymorphisms (SNPs) within IL-33 have recently been reported to be associated with risk of AD in Caucasian populations. 20708824 2012
dbSNP: rs1048274
rs1048274
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C0038013
Disease:
Ankylosing spondylitis
0.010 GeneticVariation BEFREE Eight SNPs in the IL-33 gene (rs1891385, rs16924144, rs2210463, rs16924159, rs10118795, rs1929992, rs10975519, and rs1048274) were genotyped by the improved multiplex ligase detection reaction (iMLDR) method in 400 patients with AS and 395 geographically and ethnically matched healthy controls. 24825247 2014
dbSNP: rs928413
rs928413
Entrez Id: 90865
Gene Symbol: IL33
IL33
CUI: C0004096
Disease:
Asthma
G 0.800 GeneticVariation GWASCAT Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. 31036433 2019
dbSNP: rs928413
rs928413
Entrez Id: 90865
Gene Symbol: IL33
IL33
CUI: C0004096
Disease:
Asthma
0.800 GeneticVariation GWASDB A large-scale, consortium-based genomewide association study of asthma. 20860503 2010
dbSNP: rs928413
rs928413
Entrez Id: 90865
Gene Symbol: IL33
IL33
CUI: C0004096
Disease:
Asthma
G 0.800 GeneticVariation GWASCAT Identification of a new locus at 16q12 associated with time to asthma onset. 27130862 2016
dbSNP: rs146597587
rs146597587
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C0004096
Disease:
Asthma
G 0.720 GeneticVariation GWASCAT Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis. 31619474 2019
dbSNP: rs146597587
rs146597587
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C0004096
Disease:
Asthma
0.720 GeneticVariation BEFREE Together these data demonstrate that rs146597587-C is a loss of function mutation and support the hypothesis that IL-33 haploinsufficiency protects against asthma. 28273074 2017
dbSNP: rs146597587
rs146597587
Entrez Id: 90865;107987046
Gene Symbol: IL33;LOC107987046
IL33;LOC107987046
CUI: C0004096
Disease:
Asthma
0.720 GeneticVariation BEFREE This includes a rare splice acceptor variant (rs146597587, MAF = 0.5%) in interleukin 33 (IL33) associated with reduced eosinophil count (P = 2.4x10-23), and lower risk of asthma (P = 2.6x10-7, odds ratio [95% confidence interval] = 0.56 [0.45-0.70]) and allergic rhinitis (P = 4.2x10-4, odds ratio = 0.55 [0.39-0.76]). 28787443 2017