ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.41+6dup

dbSNP: rs1479180367
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001667003 SCV001885763 likely benign not provided 2019-03-14 criteria provided, single submitter clinical testing
Invitae RCV002073137 SCV002352663 likely benign Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 2022-10-24 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446860 SCV004173869 likely benign Dilated cardiomyopathy 1D 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446861 SCV004173870 likely benign Cardiomyopathy, familial restrictive, 3 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446859 SCV004173871 likely benign Hypertrophic cardiomyopathy 2 2023-04-11 criteria provided, single submitter clinical testing

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