ClinVar Miner

List of variants reported as likely benign for Peroxisome biogenesis disorder 7A by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP
NM_001127649.3(PEX26):c.*114C>T rs45500699
NM_001127649.3(PEX26):c.*1740C>G rs139987168
NM_001127649.3(PEX26):c.*2162G>A rs45489191
NM_001127649.3(PEX26):c.*2311G>T rs74714634
NM_001127649.3(PEX26):c.*2703G>A rs0
NM_001127649.3(PEX26):c.*279G>A rs0
NM_001127649.3(PEX26):c.*566T>C rs0
NM_001127649.3(PEX26):c.*925A>G rs115277831
NM_001127649.3(PEX26):c.-363G>C rs138787474
NM_001127649.3(PEX26):c.130C>T (p.Leu44Phe) rs150895887
NM_001127649.3(PEX26):c.457C>G (p.Leu153Val) rs12484657
NM_001127649.3(PEX26):c.815-13C>T rs139370593

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.