ClinVar Miner

List of variants in gene combination PEX10, PLCH2 reported as likely pathogenic for Peroxisome biogenesis disorder 6A; Peroxisome biogenesis disorder 6B

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
Download table as spreadsheet
HGVS dbSNP
NM_002617.3(PEX10):c.20del (p.Ser7fs) rs1553232926
NM_153818.1(PEX10):c.1A>G (p.Met1Val) rs886041314

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.