Variants
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not specified

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Description

The term 'not specified' was created for use in ClinVar so that submitters can convey the concept that a variant is benign, likely benign, or of uncertain significance for an unspecified set of disorders. This usage was introduced in 2014 to replace AllHighlyPenetrant.

NCBI curation

  • Mode of Inheritance

    VARIANTS

    95,424

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    Genes

      External Links

      • OMIM
      • Orphanet
      • HPO
      • Medgen

        CN169374

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