ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.550-14T>C

gnomAD frequency: 0.00001  dbSNP: rs758992431
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001183017 SCV001348664 likely benign Cardiomyopathy 2019-09-09 criteria provided, single submitter clinical testing
GeneDx RCV001664737 SCV001872353 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV002068344 SCV002481084 likely benign Hypertrophic cardiomyopathy 2024-01-21 criteria provided, single submitter clinical testing

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