ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.373-13C>T

gnomAD frequency: 0.00003  dbSNP: rs771031464
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002180759 SCV002360029 likely benign Hypertrophic cardiomyopathy 2023-08-09 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003533102 SCV004359901 likely benign Cardiomyopathy 2022-12-13 criteria provided, single submitter clinical testing

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