|
Asthma
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
But, we observed that the A-384G polymorphism of Eotaxin 1 gene and T51C polymorphism of CCR3 gene are not associated with asthma.
|
17845580 |
2007 |
|
Asthma
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
In conclusion, a significant association between asthma and CCR3 T51C polymorphism localized on chromosome 3p21 was found.
|
11307756 |
2001 |
|
Asthma
|
0.400 |
GeneticVariation
|
disease |
GWASDB |
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.
|
21150878 |
2011 |
|
Asthma
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Although polymorphisms in CCR3 were not associated with asthma susceptibility, the CCR3 haplotype ht2 showed a negative gene dose effect on the eosinophil count (P = .003-.009).
|
17983872 |
2007 |
|
Asthma
|
0.400 |
GeneticVariation
|
disease |
LHGDN |
But, we observed that the A-384G polymorphism of Eotaxin 1 gene and T51C polymorphism of CCR3 gene are not associated with asthma.
|
17845580 |
2007 |
|
HIV Infections
|
0.320 |
GeneticVariation
|
group |
BEFREE |
Further study will be of interest to test whether CCR3-C218S variation or any of the CCR4 variations has a significant role in rendering susceptibility to immunological diseases or resistance to HIV infection.
|
11196669 |
1999 |
|
HIV Infections
|
0.320 |
GeneticVariation
|
group |
BEFREE |
The CCR3 rs3091250 [TT, adjusted odds ratio (AOR): 2.147, 95% confidence interval (CI) 1.076-4.287, P = 0.030], CCR8 rs2853699 (GC/CC, AOR: 1.577, 95% CI 1.049-2.371, P = 0.029), CXCL10 rs56061981 (CT/TT, AOR: 1.819, 95% CI 1.074-3.081, P = 0.026) and CCL22 rs4359426 (CA/AA, AOR: 1.887, 95% CI 1.021-3.487, P = 0.043) polymorphisms were associated with susceptibility to HIV infection.
|
28358741 |
2017 |
|
Rheumatoid Arthritis
|
0.140 |
GeneticVariation
|
disease |
GWASCAT |
Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis.
|
26546613 |
2016 |
|
Autoimmune Diseases
|
0.130 |
GeneticVariation
|
group |
BEFREE |
In this study, variation screening of the entire coding regions of CCR3 and CCR4 was performed, and possible association with several autoimmune diseases was tested, using the genomic DNA from 304 Japanese healthy individuals and 272 Japanese patients with rheumatic diseases.
|
11196669 |
1999 |
|
Autoimmune Diseases
|
0.130 |
GeneticVariation
|
group |
BEFREE |
Children with multiple autoimmune diseases showed nominal association with RGS1 (rs2816316), and children coming from an autoimmune family with rs11711054 (CCR3-CCR5).
|
29182645 |
2017 |
|
Autoimmune Diseases
|
0.130 |
GeneticVariation
|
group |
GWASDB |
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.
|
21383967 |
2011 |
|
Celiac Disease
|
0.130 |
GeneticVariation
|
disease |
GWASDB |
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
|
22057235 |
2011 |
|
Celiac Disease
|
0.130 |
GeneticVariation
|
disease |
GWASDB |
Multiple common variants for celiac disease influencing immune gene expression.
|
20190752 |
2010 |
|
Celiac Disease
|
0.130 |
GeneticVariation
|
disease |
GWASCAT |
Multiple common variants for celiac disease influencing immune gene expression.
|
20190752 |
2010 |
|
Celiac Disease
|
0.130 |
GeneticVariation
|
disease |
GWASCAT |
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
|
22057235 |
2011 |
|
Celiac Disease
|
0.130 |
GeneticVariation
|
disease |
GWASCAT |
Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis.
|
26546613 |
2016 |
|
Celiac Disease
|
0.130 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.
|
24999842 |
2014 |
|
Celiac Disease
|
0.130 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.
|
24999842 |
2014 |
|
Celiac Disease
|
0.130 |
GeneticVariation
|
disease |
BEFREE |
This meta-analysis provides robust estimates that IL18RAP rs917997 and CCR3 rs6441961 are potential risk factors for celiac disease in European populations.
|
26289103 |
2015 |
|
Multiple Sclerosis
|
0.130 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
|
22190364 |
2011 |
|
Behcet Syndrome
|
0.120 |
GeneticVariation
|
disease |
BEFREE |
First stage analysis showed that ten SNPs, located in 3'UTR, 5'UTR in CCR1 or 5'UTR in CCR3, were significantly associated with Behçet's disease (P(c) = 0.018 to 1.3 × 10(-3)).
|
22829007 |
2012 |
|
Behcet Syndrome
|
0.120 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.
|
23291587 |
2013 |
|
Behcet Syndrome
|
0.120 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.
|
23291587 |
2013 |
|
Immune System Diseases
|
0.110 |
GeneticVariation
|
group |
BEFREE |
Further study will be of interest to test whether CCR3-C218S variation or any of the CCR4 variations has a significant role in rendering susceptibility to immunological diseases or resistance to HIV infection.
|
11196669 |
1999 |
|
Immune System Diseases
|
0.110 |
GeneticVariation
|
group |
GWASDB |
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.
|
21383967 |
2011 |