Annotation Detail
Information
- Associated Genes
- HBB LOC106099062 LOC107133510
- Associated Variants
-
HBB c.-137C>A
(
ENST00000647020.1 )
HBB c.-137C>A ( ENST00000647020.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000518.5(HBB):c.-137C>A AND not provided
- ClinVar Allele ID
- 44949
- ClinVar RefSeq Alternation Syntax
- NM_000518.5:c.-137C>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2024-01-02
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000506877
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs