CCR3, C-C motif chemokine receptor 3, 1232

N. diseases: 149; N. variants: 16
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7616215
rs7616215
Entrez Id: 1232;105377067
Gene Symbol: CCR3;LOC105377067
CCR3;LOC105377067
CUI: C0004943
Disease:
Behcet Syndrome 		0.810 GeneticVariation BEFREE Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ). 26097239 2015
dbSNP: rs7616215
rs7616215
Entrez Id: 1232;105377067
Gene Symbol: CCR3;LOC105377067
CCR3;LOC105377067
CUI: C0004943
Disease:
Behcet Syndrome 		C 0.810 GeneticVariation GWASCAT Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587 2013
dbSNP: rs7616215
rs7616215
Entrez Id: 1232;105377067
Gene Symbol: CCR3;LOC105377067
CCR3;LOC105377067
CUI: C0004943
Disease:
Behcet Syndrome 		C 0.810 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587 2013
dbSNP: rs13096142
rs13096142
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0007570
Disease:
Celiac Disease 		0.800 GeneticVariation GWASDB Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. 24999842 2014
dbSNP: rs13096142
rs13096142
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0007570
Disease:
Celiac Disease 		0.800 GeneticVariation GWASCAT Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. 24999842 2014
dbSNP: rs79893749
rs79893749
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C3898105
Disease:
Oligoarticular Juvenile Idiopathic Arthritis 		0.800 GeneticVariation GWASCAT Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. 23603761 2013
dbSNP: rs79893749
rs79893749
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C3898105
Disease:
Oligoarticular Juvenile Idiopathic Arthritis 		0.800 GeneticVariation GWASDB Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. 23603761 2013
dbSNP: rs7616215
rs7616215
Entrez Id: 1232;105377067
Gene Symbol: CCR3;LOC105377067
CCR3;LOC105377067
CUI: C0007570
Disease:
Celiac Disease 		C 0.800 GeneticVariation GWASCAT Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. 22057235 2011
dbSNP: rs7616215
rs7616215
Entrez Id: 1232;105377067
Gene Symbol: CCR3;LOC105377067
CCR3;LOC105377067
CUI: C0007570
Disease:
Celiac Disease 		0.800 GeneticVariation GWASDB Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. 22057235 2011
dbSNP: rs13098911
rs13098911
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0007570
Disease:
Celiac Disease 		A 0.800 GeneticVariation GWASCAT Multiple common variants for celiac disease influencing immune gene expression. 20190752 2010
dbSNP: rs13098911
rs13098911
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0007570
Disease:
Celiac Disease 		A 0.800 GeneticVariation GWASDB Multiple common variants for celiac disease influencing immune gene expression. 20190752 2010
dbSNP: rs34611049
rs34611049
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs75526024
rs75526024
Entrez Id: 1230;1232
Gene Symbol: CCR1;CCR3
CCR1;CCR3
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13325613
rs13325613
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0200637
Disease:
Monocyte 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: rs13325613
rs13325613
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0750880
Disease:
Monocyte count result 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3181077
rs3181077
Entrez Id: 1230;1232
Gene Symbol: CCR1;CCR3
CCR1;CCR3
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: rs67676925
rs67676925
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0007570
Disease:
Celiac Disease 		0.700 GeneticVariation GWASCAT Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis. 26546613 2016
dbSNP: rs67676925
rs67676925
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASCAT Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis. 26546613 2016
dbSNP: rs79893749
rs79893749
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C1858558
Disease:
Rheumatoid Arthritis, Systemic Juvenile 		0.700 GeneticVariation GWASCAT Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. 23603761 2013
dbSNP: rs79893749
rs79893749
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C2931171
Disease:
Juvenile pauciarticular chronic arthritis 		0.700 GeneticVariation GWASCAT Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. 23603761 2013
dbSNP: rs79893749
rs79893749
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C3890205
Disease:
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative 		0.700 GeneticVariation GWASCAT Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. 23603761 2013
dbSNP: rs79893749
rs79893749
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0087031
Disease:
Juvenile-Onset Still Disease 		0.700 GeneticVariation GWASCAT Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. 23603761 2013
dbSNP: rs79893749
rs79893749
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C1384600
Disease:
Systemic onset juvenile chronic arthritis 		0.700 GeneticVariation GWASCAT Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. 23603761 2013
dbSNP: rs12636651
rs12636651
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0162701
Disease:
Polysomnography 		G 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs7652290
rs7652290
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0162701
Disease:
Polysomnography 		0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012