ClinVar Miner

Submissions for variant NM_004992.3(MECP2):c.377+22C>G (rs2075597)

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
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000168680 SCV001159121 benign not specified 2018-10-18 criteria provided, single submitter clinical testing
RettBASE RCV000144101 SCV000189177 not provided not provided no assertion provided not provided
RettBASE RCV000168680 SCV000222406 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.