ClinVar Miner

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

Included ClinVar conditions (3):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000262.3(NAGA):c.*555C>T	rs141688392	0.00168
NM_000262.3(NAGA):c.*1311T>C	rs185586436	0.00142

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