Hemoglobinopathy Panel
The hemoglobin genes and variants behind the most common inherited hemoglobin disorders, including the sickle cell variant (HbS) in HBB.
2 genes · 2 variants
HBBgene ↗
hemoglobin subunit beta
HBB is a human protein-coding gene.
HBA1gene ↗
hemoglobin subunit alpha 1
HBA1 is a human protein-coding gene.
rs334variant ↗
HBB · p.Glu7Val
rs334 is a genetic variant located in the HBB gene.
rs33930165variant ↗
HBB · p.Glu7Lys
rs33930165 is a genetic variant located in the HBB gene.
Educational information only — not medical advice, a diagnosis, or a clinical recommendation. This panel is a curated grouping of public-record gene and variant pages for reference; it does not reflect your own genome or personal risk. Consult a qualified genetics professional or genetic counselor for interpretation relevant to you.