ClinVar Miner

Submissions for variant NM_002471.3(MYH6):c.4047C>T (p.Tyr1349=) (rs570555040)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000242060 SCV000319719 likely benign Cardiovascular phenotype 2015-05-21 criteria provided, single submitter clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute RCV001256808 SCV001433263 likely benign not specified 2019-04-30 criteria provided, single submitter clinical testing

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