ClinVar Miner

Submissions for variant NM_004992.3(MECP2):c.377+28A>G (rs185036026)

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
Molecular Genetics Laboratory,Children's Mercy Hospital and Clinics RCV000172865 SCV000223851 benign Rett syndrome criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000168681 SCV001158762 benign not specified 2018-10-22 criteria provided, single submitter clinical testing
RettBASE RCV000144104 SCV000189180 not provided not provided no assertion provided not provided
RettBASE RCV000168681 SCV000222408 benign not specified 2013-12-05 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.