ClinVar Miner

Submissions for variant NM_016203.4(PRKAG2):c.642G>A (p.Arg214=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004807793 SCV005429725 likely benign Hypertrophic cardiomyopathy 2024-02-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005105220 SCV005800240 likely benign Lethal congenital glycogen storage disease of heart 2024-07-17 criteria provided, single submitter clinical testing

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