ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.105G>A (p.Arg35=)

dbSNP: rs2142869770
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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 RCV002120122 SCV002402089 likely benign Hypertrophic cardiomyopathy 2021-11-10 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002120122 SCV005430108 likely benign Hypertrophic cardiomyopathy 2024-05-30 criteria provided, single submitter clinical testing

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