ClinVar Miner

Submissions for variant NM_001110792.2(MECP2):c.868G>A (p.Ala290Thr) (rs782086416)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostics Lab,Nemours Alfred I. duPont Hospital for Children RCV000445578 SCV000537178 likely benign Rett syndrome 2015-07-09 criteria provided, single submitter clinical testing
RettBASE RCV000170098 SCV000222418 benign not specified 2014-02-05 no assertion criteria provided curation

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.