ClinVar Miner

Submissions for variant NM_018249.6(CDK5RAP2):c.4605-11G>C

gnomAD frequency: 0.00101  dbSNP: rs193196156
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001566202 SCV001789685 likely benign not provided 2019-08-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001566202 SCV002407209 benign not provided 2024-01-13 criteria provided, single submitter clinical testing

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