ClinVar Miner

Submissions for variant NM_001080414.4(CCDC88C):c.3320ACA[1] (p.Asn1108del)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein RCV002291135 SCV002583397 uncertain significance Spinocerebellar ataxia type 40 2022-02-01 no assertion criteria provided clinical testing

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