ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.1223+29G>A

gnomAD frequency: 0.08776  dbSNP: rs11570078
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000168767 SCV000303183 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001711341 SCV001940793 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001775659 SCV002014341 benign Left ventricular noncompaction 10 2021-09-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001775658 SCV002014343 benign Hypertrophic cardiomyopathy 4 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001711341 SCV005320306 benign not provided criteria provided, single submitter not provided
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000168767 SCV001957168 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000168767 SCV001970371 benign not specified no assertion criteria provided clinical testing

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