ClinVar Miner

Submissions for variant NM_016203.4(PRKAG2):c.618G>T (p.Pro206=)

dbSNP: rs145827515
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Total submissions: 3
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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 RCV000038950 SCV000062628 likely benign not specified 2008-10-07 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001526074 SCV001736349 likely benign Cardiomyopathy 2020-12-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003617795 SCV004548445 likely benign Lethal congenital glycogen storage disease of heart 2024-01-05 criteria provided, single submitter clinical testing

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