ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.2335-8C>G

gnomAD frequency: 0.00001  dbSNP: rs561964101
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001191600 SCV001359474 likely benign Cardiomyopathy 2018-12-01 criteria provided, single submitter clinical testing
Invitae RCV001457879 SCV001661689 likely benign Arrhythmogenic right ventricular dysplasia 10 2023-11-24 criteria provided, single submitter clinical testing

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