ClinVar Miner

Submissions for variant NM_018249.6(CDK5RAP2):c.879+26G>T

dbSNP: rs41305509
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001650992 SCV001867987 benign not provided 2018-07-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001650992 SCV005321082 benign not provided criteria provided, single submitter not provided
Genetic Services Laboratory, University of Chicago RCV000145508 SCV000192596 likely benign not specified no assertion criteria provided clinical testing

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