ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.369T>C (p.Ala123=)

dbSNP: rs2136356303
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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 RCV002203334 SCV002488200 likely benign Multiple endocrine neoplasia type 4 2022-08-31 criteria provided, single submitter clinical testing

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