ClinVar Miner

Submissions for variant NM_016203.4(PRKAG2):c.320C>G (p.Pro107Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002290199 SCV002579363 uncertain significance Hypertrophic cardiomyopathy 6 2021-10-22 criteria provided, single submitter clinical testing

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