ClinVar Miner

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

dbSNP: rs774316050
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Total submissions: 2
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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
Arcensus RCV002466261 SCV002564551 likely pathogenic Hypertrophic cardiomyopathy 4 2013-02-01 criteria provided, single submitter clinical testing

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