ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.348G>C (p.Ala116=)

dbSNP: rs1365789536
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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 RCV001415852 SCV001618021 likely benign Multiple endocrine neoplasia type 4 2020-09-16 criteria provided, single submitter clinical testing

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