Submissions for variant NM_000257.4(MYH7):c.2923-18G>A

gnomAD frequency: 0.04825  dbSNP: rs7157087

Total submissions: 9

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
PreventionGenetics, part of Exact Sciences	RCV000168881	SCV000303218	benign	not specified		criteria provided, single submitter	clinical testing
GeneDx	RCV001711451	SCV001940822	benign	not provided	2015-03-03	criteria provided, single submitter	clinical testing
Invitae	RCV002054008	SCV002444781	benign	Hypertrophic cardiomyopathy	2024-02-01	criteria provided, single submitter	clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV000168881	SCV001743022	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics, Academic Medical Center	RCV000168881	SCV001923350	benign	not specified		no assertion criteria provided	clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+	RCV000168881	SCV001954881	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center	RCV000168881	SCV001968962	benign	not specified		no assertion criteria provided	clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC)	RCV001711451	SCV002036996	likely benign	not provided		no assertion criteria provided	clinical testing
Cohesion Phenomics	RCV003126563	SCV003803022	benign	Cardiomyopathy	2022-10-10	no assertion criteria provided	clinical testing