List of variants in gene NAGA reported as likely benign by GeneDx

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000262.3(NAGA):c.1101+144C>G	rs58802487	0.00826
NM_000262.3(NAGA):c.*170G>A	rs142863061	0.00626
NM_000262.3(NAGA):c.*161T>C	rs150991002	0.00559
NM_000262.3(NAGA):c.1102-55_1102-54dup	rs138095593

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