ClinVar Miner

Submissions for variant NM_000297.4(PKD2):c.1549-4T>C

gnomAD frequency: 0.00007  dbSNP: rs374450718
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000254194 SCV000303529 likely benign not specified criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000725986 SCV000341030 uncertain significance not provided 2016-04-04 criteria provided, single submitter clinical testing
Invitae RCV002057336 SCV002361693 likely benign Autosomal dominant polycystic kidney disease 2023-12-02 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.