Annotation Detail
Information
- Associated Genes
- HBB LOC106099062 LOC107133510
- Associated Variants
-
HBB p.Val24del (p.V24del)
(
ENST00000485743.1,
ENST00000335295.4,
ENST00000647020.1 )
HBB p.Val24del (p.V24del) ( ENST00000335295.4, ENST00000485743.1, ENST00000647020.1 ) - Associated Disease
- hemoglobinopathy
- Source Database
- ClinVar
- Description
- NM_000518.5(HBB):c.71_73del (p.Val24del) AND Hemoglobinopathy
- ClinVar Allele ID
- 30205
- ClinVar RefSeq Alternation Syntax
- NM_000518.5:c.71_73del
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 1988-06-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000016337
- ClinVar Disease
- Hemoglobinopathy
- Observed Origin Sample
- germline
- Pubmed
- 5919752
- Pubmed
- 3391614
Drugs