ClinVar Miner

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

dbSNP: 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 RCV005400730 SCV000740375 likely pathogenic Cardiovascular phenotype 2025-02-11 criteria provided, single submitter clinical testing

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