Variant (rsID / SNP)

rs1024611

rs1024611 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCL2. Location: chromosome 17, position 32,579,788. Clinical significance in the table: Pathogenic; risk factor.

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Reference-table entries

CCL2Pathogenic

Clinical significance (as recorded): Pathogenic; risk factor
Variant type: single nucleotide variant
Chromosome / position: 17:32579788
Cytoband: 17q12
HGVS: NG_012123.1:g.2493A>G

Associated conditions / phenotypes

Spina bifida, susceptibility to|Coronary artery disease, development of, in hiv|Coronary artery disease, modifier of|Mycobacterium tuberculosis, susceptibility to

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.