Dominant beta-thalassemia: genes and variants

Dominant beta-thalassemia is linked to 1 analyzed protein (HBB). 11 DNA variants are known to cause it; 4 more are uncertain, and 0 of those already look disease-causing on computable evidence.

Last updated 2026-09-30. Research information, not medical advice.

Genes linked to Dominant beta-thalassemia

Known disease-causing variants in Dominant beta-thalassemia

VariantPositionProtein partClinical label
HBB M1I1Disease-causing (★★)
HBB A116D116GlobinDisease-causing (★★)
HBB E7V7GlobinDisease-causing (★★)
HBB E7K7GlobinDisease-causing (★★)
HBB M1V1Disease-causing (★★)
HBB E27K27GlobinDisease-causing (★★)
HBB L69F69GlobinDisease-causing (★★)
HBB Y146N146GlobinDisease-causing (★★)
HBB E122K122GlobinDisease-causing (★★)
HBB A116P116GlobinDisease-causing (★)
HBB A54T54GlobinDisease-causing (★)

Which prediction tools work for Dominant beta-thalassemia

How often each tool ranks a disease-causing variant above a harmless one (AUROC × 100).

Same protein, different disease

Diseases related to Dominant beta-thalassemia

Frequently asked questions

Which genes are linked to Dominant beta-thalassemia?

In CATVariant, Dominant beta-thalassemia is linked to 1 analyzed protein: HBB (Hemoglobin subunit beta).

How many genetic variants are linked to Dominant beta-thalassemia?

19 variants: 11 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 4 are of uncertain significance or have conflicting reports.

Which uncertain variants in Dominant beta-thalassemia look disease-causing?

None of the uncertain variants currently reaches the likely-pathogenic range on computable evidence alone.

Which variant effect predictor works best for Dominant beta-thalassemia?

Among tools not trained on clinical labels, AlphaMissense separates this disease's known disease-causing variants from harmless ones best (AUROC 0.64, based on 11 disease-causing and 19 harmless variants).

About this data

Variant–disease links come from ClinVar, Open Targets and UniProt, pooled from the latest public CATVariant analysis of each human protein. Evidence scores use the ACMG/AMP Bayesian points scale with computable criteria only (position among known disease variants, rarity in gnomAD, calibrated predictors, deep mutational scanning); there is no family or patient data, so they prioritise variants for expert review and never classify them.

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