ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.851+11C>T

gnomAD frequency: 0.00001  dbSNP: rs747300127
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001595854 SCV001829029 benign not provided 2017-03-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002070464 SCV002398833 likely benign Hypertrophic cardiomyopathy 2024-11-11 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001701206 SCV001923730 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001595854 SCV001958483 likely benign not provided no assertion criteria provided clinical testing

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