ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.5696T>C (p.Val1899Ala)

dbSNP: rs727504384
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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 RCV000154543 SCV000204216 uncertain significance not specified 2013-02-14 no assertion criteria provided clinical testing proposed classification - variant undergoing re-assessment, contact laboratory

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