Annotation Detail
Information
- Associated Genes
- CCL11
- Associated Variants
-
CCL11 p.Ala23Thr (p.A23T)
(
ENST00000305869.4 )
CCL11 p.Ala23Thr (p.A23T) ( ENST00000305869.4 ) - Associated Disease
- CCL11-related disorder
- Source Database
- ClinVar
- Description
- NM_002986.3(CCL11):c.67G>A (p.Ala23Thr) AND CCL11-related disorder
- ClinVar Allele ID
- 3193540
- ClinVar RefSeq Alternation Syntax
- NM_002986.3:c.67G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2019-10-25
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003974708
- ClinVar Disease
- CCL11-related disorder
- Observed Origin Sample
- germline
Drugs