ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.1798C>T (p.Pro600Ser)

dbSNP: rs397516123
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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, Mass General Brigham Personalized Medicine RCV000035749 SCV000059400 likely pathogenic Primary dilated cardiomyopathy 2014-01-03 criteria provided, single submitter clinical testing proposed classification - variant undergoing re-assessment, contact laboratory

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