List of variants reported as likely pathogenic for Pettigrew syndrome

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: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001079872.2(CUL4B):c.2633G>A (p.Arg878Gln)	rs1556173896
NM_001272071.2(AP1S2):c.-1+1G>A	rs1934288587
NM_001272071.2(AP1S2):c.21del (p.Phe7fs)	rs2519929822
NM_001272071.2(AP1S2):c.321_334del (p.Glu107fs)	rs1933972061
NM_001272071.2(AP1S2):c.357del (p.Glu121fs)

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.