Submissions for variant NM_007078.3(LDB3):c.896+6669TC[11]

dbSNP: rs71019410

Total submissions: 7

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	RCV000036852	SCV000060507	likely benign	not specified	2011-10-20	criteria provided, single submitter	clinical testing
Genetic Services Laboratory, University of Chicago	RCV000036852	SCV000595566	likely benign	not specified	2016-04-29	criteria provided, single submitter	clinical testing
GeneDx	RCV001610321	SCV001839993	benign	not provided	2019-08-18	criteria provided, single submitter	clinical testing
Invitae	RCV003502512	SCV004282911	benign	Myofibrillar myopathy 4	2023-04-18	criteria provided, single submitter	clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV000036852	SCV001743060	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics, Academic Medical Center	RCV000036852	SCV001923879	benign	not specified		no assertion criteria provided	clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+	RCV001610321	SCV001957495	likely benign	not provided		no assertion criteria provided	clinical testing