Annotation Detail
Information
- Associated Genes
- HBB LOC106099062 LOC107133510
- Associated Variants
-
HBB p.Leu69Phe (p.L69F)
(
ENST00000335295.4,
ENST00000485743.1,
ENST00000647020.1 )
HBB p.Leu69Phe (p.L69F) ( ENST00000335295.4, ENST00000485743.1, ENST00000647020.1 ) - Associated Disease
- Erythrocytosis, familial, 6 Hb SS disease Beta-thalassemia HBB/LCRB Dominant beta-thalassemia Methemoglobinemia, beta-globin type alpha thalassemia Hereditary persistence of fetal hemoglobin Malaria, susceptibility to Heinz body anemia
- Source Database
- ClinVar
- Description
- NM_000518.5(HBB):c.205C>T (p.Leu69Phe) AND multiple conditions
- ClinVar Allele ID
- 30652
- ClinVar RefSeq Alternation Syntax
- NM_000518.5:c.205C>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2021-07-06
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002482878
- 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