ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.800-11A>G

gnomAD frequency: 0.81807  dbSNP: rs434273
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Total submissions: 9
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000037540 SCV000061198 benign not specified 2011-09-16 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000037540 SCV000308992 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001610329 SCV001159481 benign not provided 2023-11-29 criteria provided, single submitter clinical testing
GeneDx RCV001610329 SCV001836240 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV002054667 SCV002428246 benign Hypertrophic cardiomyopathy 14 2024-02-01 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000037540 SCV001742959 benign not specified no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000037540 SCV001925133 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000037540 SCV001955533 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000037540 SCV001964284 benign not specified no assertion criteria provided clinical testing

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