ClinVar Miner

List of variants in gene NAGLU reported as likely benign for Sanfilippo syndrome

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000263.3(NAGLU):c.-138A>G	rs76407245	0.06051
NM_000263.3(NAGLU):c.-200G>C	rs114904267	0.01366

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