ClinVar Miner

Submissions for variant NM_004655.4(AXIN2):c.-116-13del

dbSNP: rs530658215
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000159784 SCV000209806 benign Hereditary cancer-predisposing syndrome 2014-01-13 criteria provided, single submitter clinical testing The variant is found in HEREDICANCER,COLO-HEREDIC panel(s).
Illumina Laboratory Services, Illumina RCV000382850 SCV000405756 likely benign Oligodontia-cancer predisposition syndrome 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498794 SCV002811791 likely benign Oligodontia-cancer predisposition syndrome; Colorectal cancer 2022-05-31 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.