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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.