ClinVar Miner

Submissions for variant NM_000553.5(WRN):c.95A>G (p.Lys32Arg) (rs34477820)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000122279 SCV000227158 benign not specified 2015-04-24 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000344080 SCV000473309 uncertain significance Werner syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000857870 SCV000554390 benign not provided 2019-03-05 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000857870 SCV001155395 uncertain significance not provided 2017-04-01 criteria provided, single submitter clinical testing
ITMI RCV000122279 SCV000086504 not provided not specified 2013-09-19 no assertion provided reference population

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.