ClinVar Miner

Submissions for variant NM_001005242.3(PKP2):c.1772G>T (p.Arg591Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ RCV003234873 SCV003932847 uncertain significance Arrhythmogenic right ventricular dysplasia 9 criteria provided, single submitter clinical testing

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