ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.3605G>A (p.Cys1202Tyr) (rs727503170)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000211729 SCV000198803 likely pathogenic Hypertrophic cardiomyopathy 2013-01-23 no assertion criteria provided clinical testing proposed classification - variant undergoing re-assessment, contact laboratory

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