ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3983-12dup

dbSNP: rs368931913
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
PreventionGenetics, part of Exact Sciences RCV000251892 SCV000305355 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001689799 SCV001912665 benign not provided 2020-07-16 criteria provided, single submitter clinical testing
Invitae RCV002057397 SCV002482665 benign Werner syndrome 2024-01-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002057397 SCV002514996 benign Werner syndrome 2021-12-05 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.