ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.631-10C>G

dbSNP: rs745848441
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001472531 SCV001676665 likely benign Arrhythmogenic right ventricular dysplasia 11 2024-10-10 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004808064 SCV005427501 likely benign Familial isolated arrhythmogenic right ventricular dysplasia 2024-07-20 criteria provided, single submitter clinical testing

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