ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.2437C>A (p.His813Asn)

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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 RCV004012523 SCV004843153 uncertain significance Familial isolated arrhythmogenic right ventricular dysplasia 2023-11-30 criteria provided, single submitter clinical testing

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