ClinVar Miner

Submissions for variant NM_001005242.3(PKP2):c.2152C>T (p.Leu718=)

dbSNP: rs1592729512
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001490972 SCV001695550 likely benign Arrhythmogenic right ventricular dysplasia 9 2018-01-06 criteria provided, single submitter clinical testing

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