ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.373-8G>A

dbSNP: rs369244036
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000629123 SCV000750038 likely benign Hypertrophic cardiomyopathy 2022-11-15 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001176830 SCV001340890 likely benign Cardiomyopathy 2018-12-21 criteria provided, single submitter clinical testing

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