ClinVar Miner

Submissions for variant NM_001127649.3(PEX26):c.48G>T (p.Gly16=)

gnomAD frequency: 0.00001  dbSNP: rs764244307
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
Eurofins Ntd Llc (ga) RCV000728127 SCV000855661 uncertain significance not provided 2017-07-10 criteria provided, single submitter clinical testing
Invitae RCV002060968 SCV002475774 likely benign Peroxisome biogenesis disorder 7A (Zellweger); Peroxisome biogenesis disorder 7B 2023-11-21 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.