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Determining the Pathogenicity of a Genomic Variant of Uncertain Significance Using CRISPR/Cas9 and Human Induced Pluripotent Stem Cells

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1. ClingenBaseline 02 Nov 2026
  
  in Baseline Annotations
  
  Determining the Pathogenicity of a Genomic Variant of Uncertain Significance Using CRISPR/Cas9 and Human Induced Pluripotent Stem Cells
  
  PMID: 29914921
  
  Gene: MYL3
  
  HGNC ID: 7584
  
  HGNC:758 Gene:MYL3 inferred_gene_hgnc:758 inferred_gene_source:hgnc_tag Cardiomyopathy Annotation
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inferred_gene_hgnc:758

Gene:MYL3

HGNC:758

inferred_gene_source:hgnc_tag

Cardiomyopathy Annotation

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ClingenBaseline

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pmc.ncbi.nlm.nih.gov/articles/PMC6298866/