Submissions for variant NM_001276345.2(TNNT2):c.610-81C>T

gnomAD frequency: 0.00831  dbSNP: rs28730745

Total submissions: 8

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	RCV001595063	SCV001159094	benign	not provided	2023-08-31	criteria provided, single submitter	clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute	RCV001001624	SCV001433307	benign	not specified	2019-08-06	criteria provided, single submitter	clinical testing
GeneDx	RCV001595063	SCV001828625	benign	not provided	2015-03-03	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV003446582	SCV004173756	benign	Dilated cardiomyopathy 1D	2023-04-11	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV003446583	SCV004173757	benign	Cardiomyopathy, familial restrictive, 3	2023-04-11	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV003446581	SCV004173758	benign	Hypertrophic cardiomyopathy 2	2023-04-11	criteria provided, single submitter	clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht	RCV001001624	SCV001930829	benign	not specified		no assertion criteria provided	clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+	RCV001001624	SCV001954210	benign	not specified		no assertion criteria provided	clinical testing