ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.852-23A>G

gnomAD frequency: 0.00010  dbSNP: rs371692788
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001590181 SCV001825939 likely benign not provided 2020-08-19 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 30297972)
Invitae RCV002592489 SCV003301296 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2022-11-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446842 SCV004173719 likely benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446843 SCV004173721 likely benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446841 SCV004173722 likely benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing

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