Variant (rsID / SNP)
rs4586
rs4586 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCL2. Location: chromosome 17, position 32,583,269. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- synonymous_variant
- Chromosome / position
- 17:32583269
- HGVS
- NM_002982.4,c.105T>C,p.Cys35Cys
- Allele change
- Synonymous_C35C
Associated conditions / phenotypes
Macular 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
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.