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

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Genetic Variants
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Sequence Interpretation
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Clinical Genomics
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Pathogenicity Prediction
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Exome Sequencing
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Mendelian Disorders
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Functional Annotations
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Variant Databases
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Phenotype Analysis
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ACMG Guidelines
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This cluster of papers focuses on the standards, guidelines, and tools for interpreting genetic variants, particularly in the context of clinical genomics and Mendelian disorders
Guidelines for understanding genetic variants and their impact on human health.
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Latest revision as of 21:05, 21 September 2024

Guidelines for understanding genetic variants and their impact on human health.
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.

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    subclass of
    genetics
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    OpenAlex ID
    T11642
    0 references
     
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