ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.336C>T (p.Ser112=)

dbSNP: rs756740369
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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 RCV003619348 SCV004478022 likely benign Multiple endocrine neoplasia type 4 2023-04-29 criteria provided, single submitter clinical testing

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