ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.1750G>T (p.Gly584Cys) (rs121913626)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute RCV000622746 SCV000740375 likely pathogenic Primary familial hypertrophic cardiomyopathy 2016-09-30 criteria provided, single submitter clinical testing

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