ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.926+1_926+5del

dbSNP: rs1555122811
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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 RCV000605059 SCV000711790 uncertain significance not specified 2019-08-13 criteria provided, single submitter clinical testing proposed classification - variant undergoing re-assessment, contact laboratory

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