ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.381C>T (p.Asp127=)

dbSNP: rs1467938762
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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 RCV001479618 SCV001683923 likely benign Multiple endocrine neoplasia type 4 2022-03-05 criteria provided, single submitter clinical testing

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