ClinVar Miner

List of variants in gene LOC130060903, NAGLU studied 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
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000263.3(NAGLU):c.-81C>T	rs189515084	0.00202
NM_000263.3(NAGLU):c.-78C>G	rs886052951
NM_000263.3(NAGLU):c.-82T>C	rs886052950

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