ClinVar Miner

Submissions for variant NM_002230.4(JUP):c.2022G>A (p.Lys674=)

dbSNP: rs1914011102
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002189825 SCV002345783 likely benign Naxos disease; Arrhythmogenic right ventricular dysplasia 12 2022-07-11 criteria provided, single submitter clinical testing

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