Standards and Guidelines for Genetic Variant Interpretation (Q168961)

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Revision as of 12:36, 8 September 2024 by Sky (talk | contribs) (‎Changed an Item: moved OpenAlex ID to its dedicated external ID datatype for consistency)
"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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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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