Annotation Detail
Information
- Associated Genes
- CCL2 LOC126862536
- Associated Variants
-
NC_000017.11:g.34252769A>G
NC_000017.11:g.34252769A>G - Associated Disease
- CCL2-related disorder
- Source Database
- ClinVar
- Description
- NC_000017.11:g.34252769A>G AND CCL2-related disorder
- ClinVar Allele ID
- 29246
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2023-07-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003974826
- ClinVar Disease
- CCL2-related disorder
- Observed Origin Sample
- germline
Drugs