ClinVar Miner

List of variants reported as pathogenic for alpha-N-acetylgalactosaminidase deficiency type 3 by OMIM

Included ClinVar conditions (4):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000262.3(NAGA):c.973G>A (p.Glu325Lys)	rs121434529	0.00219
NM_000262.3(NAGA):c.479C>G (p.Ser160Cys)	rs121434532	0.00049

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