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  2. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Hypertrophic cardiomyopathy clinical phenotype is independent of gene mutation and mutation dosage
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    1. ClingenBaseline 24 Oct 2026

      CasePT-111: United States

      CasePresentingHPOs: HP:0001639 (Hypertrophic cardiomyopathy)

      HPOsFreeText: N/A

      CaseNotHPOs: HP:0001650, HP:0001658 (Aortic valve stenosis, Myocardial infarction)

      NotHPOsFreeText: N/A

      CaseAddInfo:

      CaseGenotypingMethod: DNA was collected from the participants using blood samples. 18 genes suspected on contributing to HCM were targeted and sequenced. The variants were then located and filtered for pathogenicity.

      Variant: NM_000257.3:c.563C>A (p.Thr188Asn)

      CAID: CA016314 https://reg.clinicalgenome.org/redmine/projects/registry/genboree_registry/allele?hgvs=NM_000257.3%3Ac.563C%3EA

      gnomAD: Not in gnomAD

      Individual CaseInfo Variant GenotypingMethod AdditionalPreviousTesting AutosomalDominant HCM FullPreviousTesting SupplementalData CA016314 inferred_gene_hgnc:7577 inferred_gene_source:CAID Cardiomyopathy Annotation
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    ncbi.nlm.nih.gov/pmc/articles/PMC5679632/