ClinVar Miner

Submissions for variant NM_005691.3(ABCC9):c.420T>C (p.Tyr140=) (rs397517189)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario RCV000769384 SCV000900776 likely benign Cardiomyopathy 2017-09-14 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000038616 SCV000062294 likely benign not specified 2010-02-10 criteria provided, single submitter clinical testing

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