ClinVar Miner

Submissions for variant NM_001110792.2(MECP2):c.414-3_419del (rs267608466)

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
RettBASE RCV000144116 SCV000189192 not provided not provided no assertion provided not provided
RettBASE RCV000170201 SCV000222530 pathogenic Severe neonatal-onset encephalopathy with microcephaly 2008-11-10 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.