ClinVar Miner

Submissions for variant NM_001271208.2(NEB):c.21856C>G (p.Gln7286Glu) (rs373946758)

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
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000724081 SCV000225728 uncertain significance not provided 2014-08-06 criteria provided, single submitter clinical testing
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia RCV000238962 SCV000297090 uncertain significance not specified 2015-11-08 criteria provided, single submitter clinical testing
Invitae RCV000724081 SCV000763029 benign not provided 2019-03-04 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000724081 SCV001152436 uncertain significance not provided 2018-07-01 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.