"PreventionGenetics, part of Exact Sciences"[submitter] AND "NAGA"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 717761	NM_000262.3(NAGA):c.1146T>C (p.Asp382=)	NAGA	Single nucleotide variant (synonymous variant)	NAGA-related disorder +1 more	GLikely benign
Select item 2905143	NM_000262.3(NAGA):c.958-7T>C	NAGA	Single nucleotide variant (intron variant)	Alpha-N-acetylgalactosaminidase deficiency type 1 +1 more	GLikely benign
Select item 900504	NM_000262.3(NAGA):c.324C>T (p.Tyr108=)	LOC126863160, NAGA	Single nucleotide variant (synonymous variant)	NAGA-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 341912	NM_000262.3(NAGA):c.280G>A (p.Asp94Asn)	LOC126863160, NAGA (D94N)	Single nucleotide variant (missense variant)	NAGA-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 341914	NM_000262.3(NAGA):c.25C>T (p.Leu9=)	LOC126863160, NAGA	Single nucleotide variant (synonymous variant)	NAGA-related disorder +3 more	GBenign/Likely benign
Select item 3041766	NM_000262.3(NAGA):c.17-268_17-247dup	NAGA	Duplication (intron variant)	NAGA-related disorder	GUncertain significance

ClinVar