ClinVar Miner

Submissions for variant NM_001005242.3(PKP2):c.105G>A (p.Glu35=)

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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 RCV004015702 SCV004836279 likely benign Arrhythmogenic right ventricular cardiomyopathy 2024-02-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005103353 SCV005818085 likely benign Arrhythmogenic right ventricular dysplasia 9 2024-12-18 criteria provided, single submitter clinical testing

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