ClinVar Miner

Submissions for variant NM_000492.4(CFTR):c.870-1G>C

dbSNP: rs1351058559
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
Counsyl RCV000670583 SCV000795452 likely pathogenic Cystic fibrosis 2017-11-08 criteria provided, single submitter clinical testing
Baylor Genetics RCV001004241 SCV001163117 pathogenic Cystic fibrosis; Congenital bilateral aplasia of vas deferens from CFTR mutation 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.