Standards and Guidelines for Genetic Variant Interpretation (Q168961): Difference between revisions

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Revision as of 12:36, 8 September 2024

"Guidelines for understanding genetic variants and their impact on human health."
  • Genetic Variants
  • Sequence Interpretation
  • Clinical Genomics
  • Pathogenicity Prediction
  • Exome Sequencing
  • Mendelian Disorders
  • Functional Annotations
  • Variant Databases
  • Phenotype Analysis
  • ACMG Guidelines
Language Label Description Also known as
English
Standards and Guidelines for Genetic Variant Interpretation
"Guidelines for understanding genetic variants and their impact on human health."
  • Genetic Variants
  • Sequence Interpretation
  • Clinical Genomics
  • Pathogenicity Prediction
  • Exome Sequencing
  • Mendelian Disorders
  • Functional Annotations
  • Variant Databases
  • Phenotype Analysis
  • ACMG Guidelines

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