ClinVar Miner

Submissions for variant NM_001005242.3(PKP2):c.784C>T (p.Leu262=)

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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 RCV004010074 SCV004816401 likely benign Arrhythmogenic right ventricular cardiomyopathy 2024-08-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005103220 SCV005813991 likely benign Arrhythmogenic right ventricular dysplasia 9 2024-06-30 criteria provided, single submitter clinical testing

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