ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.834C>T (p.Ile278=)

dbSNP: rs1278830616
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001805719 SCV002051904 likely benign Cardiomyopathy 2021-04-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002077258 SCV002473764 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2021-10-27 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451952 SCV004180516 likely benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451953 SCV004180517 likely benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003451951 SCV004180518 likely benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing

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