Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction: genes and variants

Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction is linked to 1 analyzed protein (ACTN2). 2 DNA variants are known to cause it; 0 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 Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction

Known disease-causing variants in Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction

VariantPositionProtein partClinical label
ACTN2 E628G628Disease-causing
ACTN2 R759T759EF-hand 1Disease-causing

Diseases related to Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction

Frequently asked questions

Which genes are linked to Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction?

In CATVariant, Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction is linked to 1 analyzed protein: ACTN2 (Alpha-actinin-2).

How many genetic variants are linked to Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction?

5 variants: 2 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 0 are of uncertain significance or have conflicting reports.

Which uncertain variants in Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction look disease-causing?

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

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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