ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.162G>A (p.Glu54=)

dbSNP: rs1592280855
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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 RCV001394501 SCV001596188 likely benign Multiple endocrine neoplasia type 4 2018-05-02 criteria provided, single submitter clinical testing

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