ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.720-13C>G

gnomAD frequency: 0.00003  dbSNP: rs377714587
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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 RCV000773321 SCV000907013 likely benign Cardiomyopathy 2018-06-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002534056 SCV003462060 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2024-10-31 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446430 SCV004173746 likely benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446431 SCV004173747 likely benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446429 SCV004173748 likely benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000773321 SCV004818000 likely benign Cardiomyopathy 2024-07-20 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005056517 SCV005726050 likely benign not specified 2024-11-21 criteria provided, single submitter clinical testing

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