ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.9195G>C (p.Val3065=) (rs9935834)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000244619 SCV000305814 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000755599 SCV000604722 benign Polycystic kidney disease, adult type 2018-12-10 criteria provided, single submitter clinical testing
Molecular Genetics of Inherited Kidney Disorders Laboratory,Garvan Institute of Medical Research RCV001254264 SCV001430181 benign Polycystic kidney disease, autosomal dominant 2019-01-01 criteria provided, single submitter research

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