ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.3853+27T>A

gnomAD frequency: 0.42245  dbSNP: rs2277475
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000247868 SCV000303227 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001668423 SCV001888457 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000247868 SCV001956745 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000247868 SCV001973029 benign not specified no assertion criteria provided clinical testing

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