ClinVar Miner

List of variants reported as uncertain significance for Peroxisome biogenesis disorder 9B by Clinical Genetics laboratory, University of Goettingen

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
Download table as spreadsheet
NM_000288.4(PEX7):c.534G>C (p.Gln178His) rs746010906

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.