ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.1882G>A (p.Gly628Arg) (rs397508316)

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 RCV000577750 SCV000924274 pathogenic Cystic fibrosis 2019-03-11 reviewed by expert panel research
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000577750 SCV000678972 not provided Cystic fibrosis no assertion provided literature only
Clinical Molecular Genetics Laboratory,Johns Hopkins All Children's Hospital RCV000577750 SCV000692324 likely pathogenic Cystic fibrosis 2015-04-23 no assertion criteria provided clinical testing
Natera, Inc. RCV000577750 SCV001460205 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.