{{Rsnum
|rsid=4586
|Gene=CCL2
|Chromosome=17
|position=34256250
|Orientation=plus
|GMAF=0.4541
|Gene_s=CCL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 11.5 | 48.7 | 39.8
| HCB | 38.7 | 46.7 | 14.6
| JPT | 39.3 | 50.9 | 9.8
| YRI | 59.2 | 35.4 | 5.4
| ASW | 36.8 | 47.4 | 15.8
| CHB | 38.7 | 46.7 | 14.6
| CHD | 33.0 | 44.0 | 22.9
| GIH | 15.8 | 50.5 | 33.7
| LWK | 43.5 | 50.9 | 5.6
| MEX | 31.0 | 48.3 | 20.7
| MKK | 39.1 | 48.1 | 12.8
| TSI | 10.8 | 50.0 | 39.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=22384203
|Title=MCP1 SNPs and Pulmonary Tuberculosis in Cohorts from West Africa, the USA and Argentina: Lack of Association or Epistasis with IL12B Polymorphisms
|OA=1
}}

{{PMID|15742444}} MCP-1 gene haplotype association in biopsy proven giant cell arteritis.

{{PMID|16672419|OA=1
}} 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|17065190}} Monocyte chemotactic protein-1 single nucleotide polymorphisms do not confer susceptibility for the development of adult onset polymyositis/dermatomyositis in UK Caucasians.

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

{{PMID|18172114|OA=1
}} Comprehensive analysis of the candidate genes CCL2, CCR2, and TLR4 in age-related macular degeneration.

{{PMID|18698231|OA=1
}} Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.

{{PMID|18940815|OA=1
}} MCP-1 promoter variant -362C associated with protection from pulmonary tuberculosis in Ghana, West Africa.

{{PMID|19506371|OA=1
}} Single nucleotide polymorphisms in monocyte chemoattractant protein-1 and its receptor act synergistically to increase the risk of carotid atherosclerosis.

{{PMID|20401335|OA=1
}} Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

{{PMID Auto
|PMID=24023637
|Title=Gender-Specific Effects of Genetic Variants within Th1 and Th17 Cell-Mediated Immune Response Genes on the Risk of Developing Rheumatoid Arthritis
|OA=1
}}

{{PMID Auto
|PMID=23848218
|Title=Predictive model for earlier diagnosis of suspected age-related macular degeneration patients.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}