ClinVar Miner

Submissions for variant NM_016203.4(PRKAG2):c.1285G>C (p.Gly429Arg)

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Total submissions: 1
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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 RCV004016875 SCV004834462 uncertain significance Hypertrophic cardiomyopathy 2024-01-11 criteria provided, single submitter clinical testing

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