List of variants in gene NAGA reported as likely pathogenic for alpha-N-acetylgalactosaminidase deficiency type 2

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

Total variants: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000262.3(NAGA):c.973G>A (p.Glu325Lys)	rs121434529	0.00225
NM_000262.3(NAGA):c.986G>A (p.Arg329Gln)	rs121434533	0.00004
NM_000262.3(NAGA):c.1101+1G>A
NM_000262.3(NAGA):c.1113dup (p.Tyr372fs)
NM_000262.3(NAGA):c.606C>A (p.Tyr202Ter)	rs779423223
NM_000262.3(NAGA):c.759+1_759+8del	rs768761898

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.