ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.610-90G>A

gnomAD frequency: 0.03251  dbSNP: rs11810834
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000771103 SCV000902761 benign Cardiomyopathy 2018-03-09 criteria provided, single submitter clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute RCV001256828 SCV001433308 benign not specified 2020-04-18 criteria provided, single submitter clinical testing
GeneDx RCV001644803 SCV001859349 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446427 SCV004173759 benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446428 SCV004173760 benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446426 SCV004173761 benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing

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