ClinVar Miner

Submissions for variant NM_004064.5(CDKN1B):c.537A>C (p.Pro179=)

dbSNP: rs2136357383
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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 RCV001442334 SCV001645283 likely benign Multiple endocrine neoplasia type 4 2019-07-23 criteria provided, single submitter clinical testing

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