ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.852-20C>A

dbSNP: rs371941585
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000625312 SCV000744864 benign Hypertrophic cardiomyopathy 4 2015-09-21 criteria provided, single submitter clinical testing
Invitae RCV002531918 SCV003265942 likely benign Hypertrophic cardiomyopathy 2024-01-22 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001700420 SCV001922032 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702821 SCV001928812 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001702821 SCV001956848 likely benign not provided no assertion criteria provided clinical testing

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