Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1420106
rs1420106
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0391826
Disease:
Lhermitte-Duclos disease
0.010 GeneticVariation BEFREE Hence, this study was performed to understand the role of 2 IL18RAP (rs1420106 and rs917997) polymorphisms and IL18RAP plasma levels in lumbar disc degeneration (LDD) in Indian population. 31147177 2019
dbSNP: rs1420106
rs1420106
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0263874
Disease:
Degeneration of lumbar intervertebral disc
0.010 GeneticVariation BEFREE Hence, this study was performed to understand the role of 2 IL18RAP (rs1420106 and rs917997) polymorphisms and IL18RAP plasma levels in lumbar disc degeneration (LDD) in Indian population. 31147177 2019
dbSNP: rs1420106
rs1420106
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0221775
Disease:
Lumbar disc disease
0.010 GeneticVariation BEFREE Hence, this study was performed to understand the role of 2 IL18RAP (rs1420106 and rs917997) polymorphisms and IL18RAP plasma levels in lumbar disc degeneration (LDD) in Indian population. 31147177 2019
dbSNP: rs1420106
rs1420106
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C2985280
Disease:
Blood Protein Measurement
G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs11681718
rs11681718
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
C 0.700 GeneticVariation GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469 2017
dbSNP: rs12997015
rs12997015
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C4553157
Disease:
Interleukin 1 Receptor-Like 1 Measurement
G 0.700 GeneticVariation GWASCAT Connecting genetic risk to disease end points through the human blood plasma proteome. 28240269 2017
dbSNP: rs2272127
rs2272127
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE rs2293225, rs2272127 and rs7559479 showed the following associations: rs7559479 G allele correlated with a higher obesity risk (P=0.01; OR=1.82; 95% CI 1.15 to 2.87 for the VALCAR group; P=0.033; OR=1.35; 95% CI 1.03 to 1.79 for the Hortega population) and higher body mass index (BMI) values (P=0.0045; P=0.1 for VALCAR and Hortega, respectively); a significant association with obesity (P=0.0024, OR=1.44, 95% CI 1.14 to 1.82) and increased BMI values (P=0.008) was found when considering both populations together. rs2293225 T allele was associated with lower obesity risk (P=0.036; OR=0.60; 95% CI 0.35 to 0.96) and lower BMI values (P=0.0038; OR=1.41) while the rs2272127 G allele was associated with lower obesity risk (P=0.028; OR=0.66; 95% CI 0.44 to 0.97) only in the VALCAR population. 29146643 2017
dbSNP: rs2293225
rs2293225
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE rs2293225, rs2272127 and rs7559479 showed the following associations: rs7559479 G allele correlated with a higher obesity risk (P=0.01; OR=1.82; 95% CI 1.15 to 2.87 for the VALCAR group; P=0.033; OR=1.35; 95% CI 1.03 to 1.79 for the Hortega population) and higher body mass index (BMI) values (P=0.0045; P=0.1 for VALCAR and Hortega, respectively); a significant association with obesity (P=0.0024, OR=1.44, 95% CI 1.14 to 1.82) and increased BMI values (P=0.008) was found when considering both populations together. rs2293225 T allele was associated with lower obesity risk (P=0.036; OR=0.60; 95% CI 0.35 to 0.96) and lower BMI values (P=0.0038; OR=1.41) while the rs2272127 G allele was associated with lower obesity risk (P=0.028; OR=0.66; 95% CI 0.44 to 0.97) only in the VALCAR population. 29146643 2017
dbSNP: rs7559479
rs7559479
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE rs2293225, rs2272127 and rs7559479 showed the following associations: rs7559479 G allele correlated with a higher obesity risk (P=0.01; OR=1.82; 95% CI 1.15 to 2.87 for the VALCAR group; P=0.033; OR=1.35; 95% CI 1.03 to 1.79 for the Hortega population) and higher body mass index (BMI) values (P=0.0045; P=0.1 for VALCAR and Hortega, respectively); a significant association with obesity (P=0.0024, OR=1.44, 95% CI 1.14 to 1.82) and increased BMI values (P=0.008) was found when considering both populations together. rs2293225 T allele was associated with lower obesity risk (P=0.036; OR=0.60; 95% CI 0.35 to 0.96) and lower BMI values (P=0.0038; OR=1.41) while the rs2272127 G allele was associated with lower obesity risk (P=0.028; OR=0.66; 95% CI 0.44 to 0.97) only in the VALCAR population. 29146643 2017
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
dbSNP: rs2058660
rs2058660
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0004943
Disease:
Behcet Syndrome
0.010 GeneticVariation BEFREE AA genotype and A allele frequency of IL-18RAP/rs2058660 was significantly decreased in BD as compared to controls. 27775096 2016
dbSNP: rs2293225
rs2293225
Entrez Id: 8807
Gene Symbol: IL18RAP
IL18RAP
CUI: C0018213
Disease:
Graves Disease
0.010 GeneticVariation BEFREE Furthermore, the haplotype GAGCCCG from ST2-IL18R1-IL18RAP gene cluster (rs6543116, rs1041973, rs1035130, rs3732127, rs1035127, rs2293225, rs917997) was associated with increased susceptibility to GD with an OR of 2.03 (P = 0.022, 95% CI = 1.07-3.86). 26566691 2016
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: 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