Submissions for variant NM_006073.4(TRDN):c.2051-19G>A

gnomAD frequency: 0.42872  dbSNP: rs7754205

Total submissions: 7

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
PreventionGenetics, part of Exact Sciences	RCV000253279	SCV000311375	benign	not specified		criteria provided, single submitter	clinical testing
GeneDx	RCV000253279	SCV000520321	benign	not specified	2016-09-21	criteria provided, single submitter	clinical testing	This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	RCV000253279	SCV001774664	benign	not specified	2021-07-08	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV001838582	SCV002098717	benign	Catecholaminergic polymorphic ventricular tachycardia 5	2021-09-10	criteria provided, single submitter	clinical testing
Labcorp Genetics (formerly Invitae), Labcorp	RCV002518636	SCV002464255	benign	Catecholaminergic polymorphic ventricular tachycardia 1	2025-02-04	criteria provided, single submitter	clinical testing
Clinical Genetics, Academic Medical Center	RCV000253279	SCV001922148	benign	not specified		no assertion criteria provided	clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV000253279	SCV001963568	benign	not specified		no assertion criteria provided	clinical testing