Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11465702
rs11465702
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE Similar patterns were observed at another correlated SNP (rs11465702, P = 0.005 and 0.006, respectively for associations with schizophrenia and HSV1 seropositivity). 18092318 2008
dbSNP: rs2272127
rs2272127
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0019348
Disease:
Herpes Simplex Infections 		0.010 GeneticVariation BEFREE Exploratory analysis revealed that rs2272127 was also associated with herpes simplex virus 1 (HSV1) seropositivity in cases (P = 0.04, OR for G allele 1.58, 95% CI: 1.04-2.39). 18092318 2008
dbSNP: rs2058660
rs2058660
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0010346
Disease:
Crohn Disease 		G 0.810 GeneticVariation GWASDB Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463 2010
dbSNP: rs2058660
rs2058660
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0010346
Disease:
Crohn Disease 		G 0.810 GeneticVariation GWASCAT Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463 2010
dbSNP: rs2310300
rs2310300
Entrez Id: 8807;100616157
Gene Symbol: IL18RAP;MIR4772
IL18RAP;MIR4772
CUI: C0004096
Disease:
Asthma 		0.700 GeneticVariation GWASDB A large-scale, consortium-based genomewide association study of asthma. 20860503 2010
dbSNP: rs3755266
rs3755266
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0004096
Disease:
Asthma 		0.700 GeneticVariation GWASDB A large-scale, consortium-based genomewide association study of asthma. 20860503 2010
dbSNP: rs13401597
rs13401597
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs2058660
rs2058660
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		0.010 GeneticVariation BEFREE Here, we conducted a multiple-stage genetic association study of 133 IBD susceptibility loci in multiple leprosy samples (totaling 4,971 leprosy cases and 5,503 controls) from a Chinese population and discovered two associations at rs2058660 on 2q12.1 (p = 4.57 × 10(-19); odds ratio [OR] = 1.30) and rs6871626 on 5q33.3 (p = 3.95 × 10(-18); OR = 0.75), implicating IL18RAP/IL18R1 and IL12B as susceptibility genes for leprosy. 23103228 2012
dbSNP: rs3771150
rs3771150
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0006287
Disease:
Bronchopulmonary Dysplasia 		0.010 GeneticVariation BEFREE Genotype analysis revealed, after multiple comparisons correction, two significant single-nucleotide polymorphism (SNPs), rs3771150 (IL-18RAP) and rs3771171 (IL-18R1), in African Americans (AAs) with BPD (vs. AAs without BPD; q < 0.05). 22289858 2012
dbSNP: rs10166330
rs10166330
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
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: rs10176820
rs10176820
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
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: rs17027166
rs17027166
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C1527304
Disease:
Allergic Reaction 		A 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs2075186
rs2075186
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
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: rs2272127
rs2272127
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
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: rs2293223
rs2293223
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
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: rs3771156
rs3771156
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
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: rs887971
rs887971
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
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: rs887972
rs887972
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C1527304
Disease:
Allergic Reaction 		A 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs2058660
rs2058660
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0010346
Disease:
Crohn Disease 		0.810 GeneticVariation BEFREE One of the strongest eQTL identified (rs2058660) is also the tagSNP of a linkage block reported to affect leprosy and Crohn's disease in opposite directions. 26259071 2015
dbSNP: rs6708413
rs6708413
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs6708413
rs6708413
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0010346
Disease:
Crohn Disease 		G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs1420106
rs1420106
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0238463
Disease:
Papillary thyroid carcinoma 		0.010 GeneticVariation BEFREE 3 SNPs of IL-18 (rs549908, rs360717, and rs187238) and one of IL-18R (rs1420106) examined in this study were significantly associated with the development of PTC. 26600055 2015
dbSNP: rs2058660
rs2058660
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0023343
Disease:
Leprosy 		0.010 GeneticVariation BEFREE One of the strongest eQTL identified (rs2058660) is also the tagSNP of a linkage block reported to affect leprosy and Crohn's disease in opposite directions. 26259071 2015
dbSNP: rs34020101
rs34020101
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0200641
Disease:
Blood basophil count (lab test) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs34020101
rs34020101
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0200638
Disease:
Eosinophil count procedure 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016