ClinVar Miner

Submissions for variant NM_001079858.3(ADGRG2):c.1731_1839+373del

dbSNP: rs1601862802
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biology Pathology Center, Lille University Hospital RCV000852394 SCV000995078 pathogenic Congenital bilateral aplasia of vas deferens from CFTR mutation 2019-07-08 criteria provided, single submitter clinical testing

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