ClinVar Miner

Submissions for variant NM_004572.3(PKP2):c.1034+10C>T (rs759397762)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000938476 SCV001084286 benign not provided 2019-02-25 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000610139 SCV000733167 likely benign Arrhythmogenic right ventricular cardiomyopathy, type 9 no assertion criteria provided clinical testing

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