ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.68-5del

dbSNP: rs2102295381
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001596766 SCV001832119 benign not provided 2015-03-03 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 25351510)
Clinical Genetics, Academic Medical Center RCV001596766 SCV001918574 likely benign not provided no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001596766 SCV001963383 likely benign not provided no assertion criteria provided clinical testing

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