ClinVar Miner

Submissions for variant NM_015404.4(WHRN):c.1486C>T (p.Leu496=)

gnomAD frequency: 0.00002  dbSNP: rs758197889
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001517740 SCV001726302 benign not provided 2023-11-24 criteria provided, single submitter clinical testing
GeneDx RCV001517740 SCV001828042 likely benign not provided 2019-02-01 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 20352026)

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