ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.52+13G>A

gnomAD frequency: 0.00004  dbSNP: rs376820377
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001699617 SCV001939233 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV002073266 SCV002361581 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2023-09-28 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446870 SCV004173859 benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446871 SCV004173860 benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446869 SCV004173861 benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001701234 SCV001919184 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001699617 SCV001926354 likely benign not provided no assertion criteria provided clinical testing

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