Submissions for variant NM_001035.3(RYR2):c.10935+18C>T

gnomAD frequency: 0.98361  dbSNP: rs2797445

Total submissions: 10

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Eurofins Ntd Llc (ga)	RCV000180072	SCV000232437	benign	not specified	2014-09-15	criteria provided, single submitter	clinical testing
PreventionGenetics, part of Exact Sciences	RCV000180072	SCV000306019	benign	not specified		criteria provided, single submitter	clinical testing
GeneDx	RCV001675660	SCV001892928	benign	not provided	2015-03-03	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV001795300	SCV002033028	benign	Arrhythmogenic right ventricular dysplasia 2	2021-11-07	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV001842796	SCV002033030	benign	Cardiac arrhythmia	2021-11-07	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV001795301	SCV002033031	benign	Catecholaminergic polymorphic ventricular tachycardia 1	2021-11-07	criteria provided, single submitter	clinical testing
Labcorp Genetics (formerly Invitae), Labcorp	RCV001795301	SCV002409621	benign	Catecholaminergic polymorphic ventricular tachycardia 1	2025-02-04	criteria provided, single submitter	clinical testing
Breakthrough Genomics, Breakthrough Genomics	RCV001675660	SCV005280790	benign	not provided		criteria provided, single submitter	not provided
Clinical Genetics, Academic Medical Center	RCV000180072	SCV001921413	benign	not specified		no assertion criteria provided	clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV000180072	SCV001963284	benign	not specified		no assertion criteria provided	clinical testing