ClinVar Miner

Submissions for variant NM_002230.4(JUP):c.1925-17C>T

dbSNP: rs1555598762
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001715460 SCV001941650 benign not provided 2015-08-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073335 SCV002344185 likely benign Naxos disease; Arrhythmogenic right ventricular dysplasia 12 2024-01-13 criteria provided, single submitter clinical testing

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