ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.164-11G>A

gnomAD frequency: 0.00001  dbSNP: rs1410150306
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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 RCV001190117 SCV001357533 likely benign Cardiomyopathy 2020-02-09 criteria provided, single submitter clinical testing
Invitae RCV002069106 SCV002453957 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2023-10-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446643 SCV004173819 likely benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446644 SCV004173821 likely benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446642 SCV004173822 likely benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing

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