Annotation Detail
Information
- Associated Genes
- CCL2
- Associated Variants
-
CCL2 p.Cys35= (p.C35=)
(
ENST00000225831.4,
ENST00000580907.6 )
CCL2 p.Cys35= (p.C35=) ( ENST00000225831.4, ENST00000580907.6 ) - Associated Disease
- CCL2-related disorder
- Source Database
- ClinVar
- Description
- NM_002982.4(CCL2):c.105T>C (p.Cys35=) AND CCL2-related disorder
- ClinVar Allele ID
- 3196821
- ClinVar RefSeq Alternation Syntax
- NM_002982.4:c.105T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2019-10-17
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003979697
- ClinVar Disease
- CCL2-related disorder
- Observed Origin Sample
- germline
Drugs