ClinVar Miner

Submissions for variant NM_001039958.1(MESP2):c.547_582del36 (p.Gln194_Gly205del) (rs749710849)

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
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000514201 SCV000609895 likely benign not provided 2017-03-10 criteria provided, single submitter clinical testing
PreventionGenetics RCV000247765 SCV000306147 benign not specified 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.