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1 Matching Annotations
  1. Oct 2026
  2. journals.plos.org journals.plos.org
    Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy
    1
    1. ClingenBaseline 24 Oct 2026
      in Baseline Annotations

      Supplementary Data: S2 Table

      Case 100: Spanish, 81yo, Male

      DiseaseAssertion: Hypertrophic Cardiomyopathy

      CasePreviousTesting: Full Testing (MYBPC3, TNNT2, TNNI3, MYL2, MYL3, TPM1, ACTC1), additional testing listed in supplementary data table S1

      CaseGenotypingMethod: genomic DNA obtained from blood or saliva, Next-gen sequencing panels of 55 or 78 genes

      Variant: NM_000257.3:c.1580C>T

      CAID: CA389050265, http://reg.clinicalgenome.org/redmine/projects/registry/genboree_registry/by_caid?caid=CA389050265

      gnomAD: n/a

      Individual CaseInfo HCM FullPreviousTesting AdditionalPreviousTesting NoInheritanceAssertion CA389050265 SupplementalData inferred_gene_hgnc:7577 inferred_gene_source:CAID Cardiomyopathy Annotation
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    Tags

    • FullPreviousTesting
    • HCM
    • inferred_gene_hgnc:7577
    • Individual
    • inferred_gene_source:CAID
    • NoInheritanceAssertion
    • AdditionalPreviousTesting
    • SupplementalData
    • Cardiomyopathy Annotation
    • CaseInfo
    • CA389050265

    Annotators

    • ClingenBaseline

    URL

    journals.plos.org/plosone/article
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