ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.711C>A (p.Tyr237Ter) (rs774316050)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Center for Human Genetics,University of Leuven	RCV000768465	SCV000886747	pathogenic	Hypertrophic cardiomyopathy	2018-10-31	criteria provided, single submitter	clinical testing

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