ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.505+39dup

dbSNP: rs747036965
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001723436 SCV001954187 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001727996 SCV001971177 benign not specified no assertion criteria provided clinical testing

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