ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.234-10T>C

dbSNP: rs1342160801
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000934255 SCV001782053 likely benign not provided 2019-03-15 criteria provided, single submitter clinical testing
Invitae RCV002066134 SCV002369639 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2021-08-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446541 SCV004173806 likely benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446542 SCV004173807 likely benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446540 SCV004173808 likely benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004003262 SCV004827651 likely benign Cardiomyopathy 2023-05-16 criteria provided, single submitter clinical testing

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