ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.42-6T>C

dbSNP: rs1660720268
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001190755 SCV001358338 likely benign Cardiomyopathy 2018-11-21 criteria provided, single submitter clinical testing
Invitae RCV002069129 SCV002474801 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2024-01-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446646 SCV004173862 likely benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446647 SCV004173863 likely benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446645 SCV004173865 likely benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702886 SCV001931625 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001702886 SCV001951276 likely benign not provided no assertion criteria provided clinical testing

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