ClinVar Miner

Submissions for variant NM_001005242.3(PKP2):c.657A>G (p.Arg219=)

dbSNP: rs750880081
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002139993 SCV002460870 likely benign Arrhythmogenic right ventricular dysplasia 9 2024-05-22 criteria provided, single submitter clinical testing

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