ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.255G>A (p.Val85=)

gnomAD frequency: 0.00001  dbSNP: rs780115529
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000646074 SCV000767831 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2023-11-27 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001805778 SCV002052355 likely benign Cardiomyopathy 2021-05-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451537 SCV004177939 likely benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451538 SCV004177940 likely benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451536 SCV004177941 likely benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001805778 SCV004831405 likely benign Cardiomyopathy 2023-06-26 criteria provided, single submitter clinical testing

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