ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.1680A>C (p.Arg560Ser) (rs397508267)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CFTR2 RCV000576677 SCV000677623 pathogenic Cystic fibrosis 2017-03-17 reviewed by expert panel research
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000576677 SCV000679119 not provided Cystic fibrosis no assertion provided literature only
Counsyl RCV000576677 SCV000792066 likely pathogenic Cystic fibrosis 2017-06-07 no assertion criteria provided clinical testing
Natera, Inc. RCV000576677 SCV001460196 pathogenic Cystic fibrosis 2020-09-16 no assertion criteria provided 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.