ClinVar Miner

Submissions for variant NM_001792.5(CDH2):c.1159-1G>A

dbSNP: rs2510799501
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Lab, University of California San Francisco RCV004017191 SCV004847112 pathogenic Arrhythmogenic right ventricular dysplasia, familial, 14 2023-05-25 criteria provided, single submitter clinical testing

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