ClinVar Miner

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

dbSNP: rs41305509
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ClinVar version:
Total submissions: 2
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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
Genetic Services Laboratory, University of Chicago RCV000145508 SCV000192596 likely benign not specified no assertion criteria provided clinical testing

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