ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.3815-66C>T

gnomAD frequency: 0.28148  dbSNP: rs2290146
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001715367 SCV001941439 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001715367 SCV005320293 benign not provided criteria provided, single submitter not provided
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001724419 SCV001957255 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001724419 SCV001963666 benign not specified no assertion criteria provided clinical testing

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