ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.610-10C>T

dbSNP: rs375547142
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000646075 SCV000767832 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2023-12-27 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV000768717 SCV000900087 uncertain significance Cardiomyopathy 2015-11-09 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000768717 SCV001351159 likely benign Cardiomyopathy 2019-12-10 criteria provided, single submitter clinical testing

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