ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.11390A>G (p.Tyr3797Cys)

dbSNP: rs138629093
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000788222 SCV000927264 likely pathogenic not provided 2017-05-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005021182 SCV005638794 likely pathogenic Polycystic kidney disease, adult type 2024-04-13 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.