Rs1024611

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Orientationminus
is asnp
is mentioned by
dbSNPrs1024611
PheGenIrs1024611
nextbiors1024611
hapmaprs1024611
1000 genomesrs1024611
hgdprs1024611
ensemblrs1024611
gopubmedrs1024611
geneviewrs1024611
scholarrs1024611
googlers1024611
pharmgkbrs1024611
gwascentralrs1024611
openSNPrs1024611
23andMers1024611
23andMe allrs1024611
SNP Nexus

SNPshotrs1024611
SNPdbers1024611
MSV3drs1024611
GeneCCL2
Chromosome17
Orientationminus
GMAF0.4054
Position32579788
ReferenceGRCh37 37.1/131
Max Magnitude2.2
Geno Mag Summary
(C;C) 2.2 increased risk of exercise induced ischemia, Increased CCL2 levels; increased rate of HIV progression
(C;T) 2 increased risk of exercise induced ischemia
(T;T) 0 normal risk
? (C;C) (C;T) (T;T) 28
rs1024611, also known as the -2578A>G SNP due to its position in the promoter of the monocyte chemoattractant protein-1 MCP-1 CCL2 gene, influences the production of its corresponding protein, a chemokine involved in inflammatory responses.

In a study focusing on 679 apparently healthy siblings of people with premature heart disease, investigators found that carriers of an rs1024611(C) allele - oriented as in dbSNP, not as published - independently predicted the risk of exercise induced ischemia in general. The odds ratio was reported to be 1.86 (CI: 1.14-3.04, p=0.014), regardless of race, age, sex and other factors. However, it is not clear if this risk carries over to individuals who lack siblings with heart disease.[PMID 16934270]

discussed in the 23andMe blog as being relevant to HIV

[PMID 19032966] rs1024611 is not associated with systemic sclerosis in a multicenter study of 345 European patients


[PMID 23166687] [The rs1024611 regulatory region polymorphism is associated with CCL2 allelic expression imbalance]

OMIM158105
DescCHEMOKINE, CC MOTIF, LIGAND 2; CCL2
Variant0003
Relatedalso
OMIM607948
DescMYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO
Variant
Relatedalso
tuberculosis


[PMID 22142522] Lack of Association between rs1024611 (-2581 A/G) Polymorphism in CC-chemokine Ligand 2 and Susceptibility to Pulmonary Tuberculosis in Zahedan, Southeast Iran


[PMID 22117412] [Association of polymorphic markers of CCL2 gene with essential hypertension]


[PMID 22384203OA-icon.png] MCP1 SNPs and Pulmonary Tuberculosis in Cohorts from West Africa, the USA and Argentina: Lack of Association or Epistasis with IL12B Polymorphisms


[PMID 22733495] Association of inflammatory chemokine gene CCL2I/D with bladder cancer risk in North Indian population

[PMID 16078996OA-icon.png] Association study of functional genetic variants of innate immunity related genes in celiac disease.

[PMID 16672419OA-icon.png] Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantation.

[PMID 16719905OA-icon.png] Association study of genetic variants of pro-inflammatory chemokine and cytokine genes in systemic lupus erythematosus.

[PMID 17062130OA-icon.png] Polymorphisms within inflammatory genes and colorectal cancer.

[PMID 17763208] Association of the -2510A/G chemokine (C-C motif) ligand 2 polymorphism with knee osteoarthritis in a Korean population.

[PMID 17848170OA-icon.png] The chemokine network. II. On how polymorphisms and alternative splicing increase the number of molecular species and configure intricate patterns of disease susceptibility.

[PMID 17903293OA-icon.png] Genome-wide association with select biomarker traits in the Framingham Heart Study.

[PMID 18464913OA-icon.png] A genome-wide association study identifies protein quantitative trait loci (pQTLs).

[PMID 18698231OA-icon.png] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.

[PMID 18940815OA-icon.png] MCP-1 promoter variant -362C associated with protection from pulmonary tuberculosis in Ghana, West Africa.

[PMID 19347053OA-icon.png] Analysis of inflammation- and atherosclerosis-related gene polymorphisms in branch retinal vein occlusion.

[PMID 19357773OA-icon.png] Common variants of inflammatory cytokine genes are associated with risk of nephropathy in type 2 diabetes among Asian Indians.

[PMID 19506371OA-icon.png] Single nucleotide polymorphisms in monocyte chemoattractant protein-1 and its receptor act synergistically to increase the risk of carotid atherosclerosis.

[PMID 20111728OA-icon.png] Joint effect of MCP-1 genotype GG and MMP-1 genotype 2G/2G increases the likelihood of developing pulmonary tuberculosis in BCG-vaccinated individuals.

[PMID 20111745OA-icon.png] Gene-gene interactions in the folate metabolic pathway and the risk of conotruncal heart defects.

[PMID 20125127] The -A2518G polymorphism of monocyte chemoattractant protein-1 is associated with Crohn's disease.

[PMID 20196868OA-icon.png] Polymorphisms in IL-1beta, vitamin D receptor Fok1, and Toll-like receptor 2 are associated with extrapulmonary tuberculosis.

[PMID 20339010] CCL2 and CCR2 polymorphisms are associated with markers of exercise-induced skeletal muscle damage.

[PMID 20622166OA-icon.png] Combined effect of inflammatory gene polymorphisms and the risk of ischemic stroke in a prospective cohort of subjects with type 2 diabetes: a Go-DARTS study.

[PMID 20725607OA-icon.png] CCL3 genotype and current depression increase risk of HIV-associated dementia.

[PMID 20811626OA-icon.png] Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.

[PMID 22425139] Monocyte chemoattractant protein-1 in schizophrenia: -2518A/G genetic variant and protein levels in Armenian population.


[PMID 23166687OA-icon.png] The rs1024611 Regulatory Region Polymorphism Is Associated with CCL2 Allelic Expression Imbalance


[PMID 23427179] Relationships of Single Nucleotide Polymorphisms of Monocyte Chemoattractant Protein 1 and Chemokine Receptor 2 With Susceptibility and Clinicopathologic Characteristics of Neoplasia of Uterine Cervix in Taiwan Women


[PMID 24023637OA-icon.png] Gender-Specific Effects of Genetic Variants within Th1 and Th17 Cell-Mediated Immune Response Genes on the Risk of Developing Rheumatoid Arthritis


[PMID 24083412] Functional Genetic Polymorphisms of Monocyte Chemoattractant Protein 1 and C-C Chemokine Receptor Type 2 in Ischemic Stroke


[PMID 24382482] Polymorphism of monocyte chemoattractant protein -1 (MCP-1 -2518 A/G) and responsiveness to hepatitis B vaccination in hemodialysis patients