ClinVar Miner

Submissions for variant NM_000038.6(APC):c.271del (p.Met91fs)

dbSNP: rs1554069710
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
GeneDx RCV000657161 SCV000778877 pathogenic not provided 2014-12-23 criteria provided, single submitter clinical testing Updated: 06/26/2014
Baylor Genetics RCV003459555 SCV004207372 likely pathogenic Familial adenomatous polyposis 1 2022-11-04 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.