ClinVar Miner

Submissions for variant NM_001005242.3(PKP2):c.1379-2011G>C

dbSNP: rs140301552
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000866961 SCV001008134 likely benign Arrhythmogenic right ventricular dysplasia 9 2024-06-11 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004002988 SCV004825399 likely benign Arrhythmogenic right ventricular cardiomyopathy 2024-05-14 criteria provided, single submitter clinical testing

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