ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.174C>A (p.Arg58=)

gnomAD frequency: 0.00002  dbSNP: rs757517265
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002096559 SCV002390953 likely benign Multiple endocrine neoplasia type 4 2023-11-02 criteria provided, single submitter clinical testing

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