ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.963G>C (p.Val321=)

dbSNP: rs1359648001
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001185916 SCV001352227 likely benign Cardiomyopathy 2019-11-12 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004008561 SCV004834697 likely benign Hypertrophic cardiomyopathy 2023-02-24 criteria provided, single submitter clinical testing

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