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Gene entry

CCL2

C-C motif chemokine ligand 2

Chromosome
17
Cytoband
17q12
Variants (rsID)
3

CCL2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q12). Its official name is “C-C motif chemokine ligand 2”. The reference table lists 3 variants (rsID) for this gene.

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Clinically classified variants

2 reference-table entries with clinical significance.

  • rs1024611Pathogenicsingle nucleotide variantSpina bifida, susceptibility to|Coronary artery disease, development of, in hiv|Coronary artery disease, modifier of|Mycobacterium tuberculosis, susceptibility to
  • rs4586Not classifiedsynonymous_variantMacular Degeneration, Age-Related, 1|Osteoarthritis|Chronic Pain|Plica Syndrome|Pulmonary Disease, Chronic Obstructive|Synovitis|Glucose Intolerance|Gestational Diabetes|Schizophrenia|Diabetes Mellitus|Gastric Cancer|Colorectal Cancer|Tuberculous Meningitis|Dermatomyositis|Polymyositis|End Stage Renal Disease|Pulmonary Tuberculosis|Myopathy

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.