ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2541C>T (p.Tyr847=)

dbSNP: rs397515974
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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 RCV001179208 SCV001343819 likely benign Cardiomyopathy 2019-07-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001487022 SCV001691505 likely benign Hypertrophic cardiomyopathy 2022-08-16 criteria provided, single submitter clinical testing

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