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

gnomAD frequency: 0.81807  dbSNP: rs434273

Total submissions: 10

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	2024-11-21	criteria provided, single submitter	clinical testing
GeneDx	RCV001610329	SCV001836240	benign	not provided	2015-03-03	criteria provided, single submitter	clinical testing
Labcorp Genetics (formerly Invitae), Labcorp	RCV002054667	SCV002428246	benign	Hypertrophic cardiomyopathy 14	2025-02-04	criteria provided, single submitter	clinical testing
Breakthrough Genomics, Breakthrough Genomics	RCV001610329	SCV005232875	benign	not provided		criteria provided, single submitter	not provided
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