ClinVar Miner

Submissions for variant NM_018249.6(CDK5RAP2):c.3537C>T (p.Tyr1179=)

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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 RCV003121992 SCV003789208 likely benign not provided 2024-09-03 criteria provided, single submitter clinical testing

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