ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.63G>A (p.Val21=)

dbSNP: rs2095900994
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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 RCV001177259 SCV001341435 likely benign Cardiomyopathy 2019-12-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002558847 SCV002948555 likely benign Hypertrophic cardiomyopathy 2022-01-05 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002558847 SCV005430110 likely benign Hypertrophic cardiomyopathy 2024-08-29 criteria provided, single submitter clinical testing

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