List of variants reported as likely pathogenic for Peroxisome biogenesis disorder, complementation group 7

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002617.4(PEX10):c.932G>A (p.Arg311Gln)	rs724160001	0.00003
NM_002617.4(PEX10):c.113-1G>A	rs867305222	0.00002
NM_002617.4(PEX10):c.827G>T (p.Cys276Phe)	rs1414973726	0.00001
NM_002617.4(PEX10):c.113-1G>C
NM_002617.4(PEX10):c.601-61G>A
NM_002617.4(PEX10):c.773_776+17del
NM_002617.4(PEX10):c.776+1G>A
NM_002617.4(PEX10):c.776+1G>C	rs869312935
NM_002617.4(PEX10):c.830T>C (p.Leu277Pro)	rs724160000
NM_002617.4(PEX10):c.916del (p.Glu306fs)	rs2100419143

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.