ClinVar Miner

Submissions for variant NM_000297.3(PKD2):c.1359A>G (p.Pro453=) (rs17013754)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 6
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000712678 SCV000843197 benign not provided 2017-09-21 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000078579 SCV000592879 benign not specified criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000078579 SCV000110435 benign not specified 2015-12-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000233733 SCV000451554 likely benign Polycystic kidney disease, autosomal dominant 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000233733 SCV000284557 benign Polycystic kidney disease, autosomal dominant 2017-08-02 criteria provided, single submitter clinical testing
PreventionGenetics RCV000078579 SCV000303526 benign not specified criteria provided, single submitter clinical testing

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.