ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.2347C>G (p.Arg783Gly)

dbSNP: rs727503258
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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 RCV000151274 SCV000199200 likely pathogenic Primary dilated cardiomyopathy 2018-11-02 criteria provided, single submitter clinical testing proposed classification - variant undergoing re-assessment, contact laboratory

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