Annotation Detail
Information
- Associated Genes
- CCL2 LOC126862536
- Associated Variants
-
NC_000017.11:g.34252769A>G
NC_000017.11:g.34252769A>G - Associated Disease
- Coronary artery disease, modifier of
- Source Database
- ClinVar
- Description
- NC_000017.11:g.34252769A>G AND Coronary artery disease, modifier of
- ClinVar Allele ID
- 29246
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2009-01-15
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000015272
- ClinVar Disease
- Coronary artery disease, modifier of
- Observed Origin Sample
- germline
- Pubmed
- 16596675
- Pubmed
- 18940815
- Pubmed
- 16352737
- Pubmed
- 15466648
- Pubmed
- 11500196
Drugs