ClinVar Miner

Submissions for variant NM_000553.4(WRN):c.3422C>T (p.Ser1141Leu) (rs139323683)

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
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000724001 SCV000228696 uncertain significance not provided 2016-04-22 criteria provided, single submitter clinical testing
ITMI RCV000122288 SCV000086515 not provided not specified 2013-09-19 no assertion provided reference population
Invitae RCV000229491 SCV000285560 benign Werner syndrome 2018-01-03 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.