ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.-8G>A

gnomAD frequency: 0.00003  dbSNP: rs773513015
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001175666 SCV001339355 likely benign Cardiomyopathy 2019-07-11 criteria provided, single submitter clinical testing
GeneDx RCV001712868 SCV001939223 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001175666 SCV002042740 uncertain significance Cardiomyopathy 2020-01-23 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004000289 SCV004828887 likely benign Hypertrophic cardiomyopathy 2024-07-23 criteria provided, single submitter clinical testing

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