ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.12133A>G (p.Ile4045Val) (rs10960)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000244151 SCV000305688 benign not specified criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000244151 SCV000592860 benign not specified 2016-04-26 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000576448 SCV000604687 benign Polycystic kidney disease, adult type 2018-07-11 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000576448 SCV000677393 benign Polycystic kidney disease, adult type 2017-05-02 criteria provided, single submitter clinical testing
Molecular Genetics of Inherited Kidney Disorders Laboratory,Garvan Institute of Medical Research RCV001254261 SCV001430178 benign Polycystic kidney disease, autosomal dominant 2019-01-01 criteria provided, single submitter research

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.