ClinVar Miner

Submissions for variant NM_001005242.3(PKP2):c.2167+8G>A

gnomAD frequency: 0.00002  dbSNP: rs371564682
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000872789 SCV001014658 likely benign Arrhythmogenic right ventricular dysplasia 9 2023-12-11 criteria provided, single submitter clinical testing

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