Annotation Detail
Information
- Associated Genes
- HBB LOC107133510 LOC110006319
- Associated Variants
-
HBB c.*110T>C
(
ENST00000335295.4,
ENST00000647020.1 )
HBB c.*110T>C ( ENST00000335295.4, ENST00000647020.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000518.5(HBB):c.*110T>C AND not provided
- ClinVar Allele ID
- 44996
- ClinVar RefSeq Alternation Syntax
- NM_000518.5:c.*110T>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-12-12
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000506540
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs