ClinVar Miner

Submissions for variant NM_018249.6(CDK5RAP2):c.4909C>T (p.Leu1637=)

dbSNP: rs1588249600
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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 RCV000937792 SCV001083585 likely benign not provided 2018-07-19 criteria provided, single submitter clinical testing

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