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rs2857656

From SNPedia

Orientationplus
Stabilizedplus
Make rs2857656(C;C)
Make rs2857656(C;G)
Make rs2857656(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position34254988
GeneCCL2
is asnp
is mentioned by
dbSNPrs2857656
ebirs2857656
HLIrs2857656
Exacrs2857656
Varsomers2857656
Maprs2857656
PheGenIrs2857656
hapmaprs2857656
1000 genomesrs2857656
hgdprs2857656
ensemblrs2857656
gopubmedrs2857656
geneviewrs2857656
scholarrs2857656
googlers2857656
pharmgkbrs2857656
gwascentralrs2857656
openSNPrs2857656
23andMers2857656
23andMe allrs2857656
SNP Nexus

SNPshotrs2857656
SNPdbers2857656
MSV3drs2857656
GWAS Ctlgrs2857656
GMAF0.4513
Max Magnitude
? (C;C) (C;G) (G;G) 28
[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 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 18940815OA-icon.png] MCP-1 promoter variant -362C associated with protection from pulmonary tuberculosis in Ghana, West Africa.

[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 23198952] Association of CXCL1 promoter polymorphism with ischaemic stroke in Korean population.