Annotation Detail
Information
- Associated Genes
- HBB LOC106099062 LOC107133510
- Associated Variants
-
HBB p.Phe42LeufsTer19 (p.F42Lfs*19)
(
ENST00000647020.1,
ENST00000335295.4,
ENST00000485743.1 )
HBB p.Phe42LeufsTer19 (p.F42Lfs*19) ( ENST00000335295.4, ENST00000485743.1, ENST00000647020.1 ) - Associated Disease
- Malaria, susceptibility to Hereditary persistence of fetal hemoglobin Erythrocytosis, familial, 6 alpha thalassemia Hb SS disease Heinz body anemia Dominant beta-thalassemia Methemoglobinemia, beta-globin type Beta-thalassemia HBB/LCRB
- Source Database
- ClinVar
- Description
- NM_000518.5(HBB):c.126_129del (p.Phe42fs) AND multiple conditions
- ClinVar Allele ID
- 30456
- ClinVar RefSeq Alternation Syntax
- NM_000518.5:c.126_129del
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-03-08
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002496380
- ClinVar Disease
- Hereditary persistence of fetal hemoglobin
- ClinVar Disease
- Beta-thalassemia HBB/LCRB
- ClinVar Disease
- Hb SS disease
- ClinVar Disease
- alpha Thalassemia
- ClinVar Disease
- Malaria, susceptibility to
- ClinVar Disease
- Erythrocytosis, familial, 6
- ClinVar Disease
- Dominant beta-thalassemia
- ClinVar Disease
- Heinz body anemia
- ClinVar Disease
- Methemoglobinemia, beta-globin type
- Observed Origin Sample
- unknown
Drugs