ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.285C>G (p.Pro95=)

dbSNP: rs780148172
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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 RCV001475406 SCV001679596 likely benign Multiple endocrine neoplasia type 4 2020-10-21 criteria provided, single submitter clinical testing

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