ClinVar Miner

Submissions for variant NM_002230.4(JUP):c.855G>C (p.Leu285=)

dbSNP: rs1392149768
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001494766 SCV001699430 likely benign Naxos disease; Arrhythmogenic right ventricular dysplasia 12 2023-03-17 criteria provided, single submitter clinical testing

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