ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.1014+7A>G

gnomAD frequency: 0.00002  dbSNP: rs756562276
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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 RCV002082919 SCV002326915 likely benign Arrhythmogenic right ventricular dysplasia 10 2022-09-28 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory - Cardiogenetics, CHU de Nantes RCV002260409 SCV002540067 uncertain significance Arrhythmogenic right ventricular cardiomyopathy 2022-06-01 criteria provided, single submitter curation

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