ClinVar Miner

Submissions for variant NM_001005242.3(PKP2):c.1520A>G (p.Asp507Gly)

dbSNP: rs1555144465
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000605535 SCV000734331 uncertain significance Arrhythmogenic right ventricular dysplasia 9 no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001701116 SCV001918198 uncertain significance not provided no assertion criteria provided clinical testing

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