ClinVar Miner

Submissions for variant NM_003392.7(WNT5A):c.*1953dup

dbSNP: rs78756487
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
Illumina Laboratory Services, Illumina RCV000312477 SCV000445617 benign Autosomal dominant Robinow syndrome 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000312477 SCV000445620 uncertain significance Autosomal dominant Robinow syndrome 1 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001691990 SCV001912654 benign not provided 2021-05-16 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.