ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.720-6_720-3del

dbSNP: rs1658597866
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001170986 SCV001333652 uncertain significance Cardiomyopathy 2017-11-03 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001170986 SCV004843085 uncertain significance Cardiomyopathy 2023-11-30 criteria provided, single submitter clinical testing

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