ClinVar Miner

Submissions for variant NM_005691.3(ABCC9):c.817-14_817-4del (rs774857795)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000463218 SCV000561927 likely benign not provided 2018-11-08 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario RCV000769382 SCV000900773 uncertain significance Cardiomyopathy 2017-02-22 criteria provided, single submitter clinical testing

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