ClinVar Miner

Submissions for variant NM_004281.3(BAG3):c.836C>A (p.Ser279Ter) (rs751261054)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute RCV000490546 SCV000577978 likely pathogenic Familial dilated cardiomyopathy 2016-07-28 criteria provided, single submitter clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute RCV000623524 SCV000740453 likely pathogenic not provided 2016-07-28 criteria provided, single submitter clinical testing

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