ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.3339C>T (p.Phe1113=)

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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 RCV002571797 SCV002937902 likely benign Hypertrophic cardiomyopathy 2022-07-25 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002571797 SCV004825334 likely benign Hypertrophic cardiomyopathy 2023-05-16 criteria provided, single submitter clinical testing

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