Variants
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Description

The term 'not provided' is registered in MedGen to support identification of submissions to ClinVar for which no condition was named when assessing the variant. 'not provided' differs from 'not specified', which is used when a variant is asserted to be benign, likely benign, or of uncertain significance for conditions that have not been specified.

NCBI curation

  • Mode of Inheritance

    VARIANTS

    313,856

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    Genes

      External Links

      • OMIM
      • Orphanet
      • HPO
      • Medgen

        CN517202

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