ClinVar Miner

List of variants in gene combination LOC130060902, NAGLU reported as uncertain significance for Sanfilippo syndrome

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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.-271A>G	rs369458319	0.00038
NM_000263.3(NAGLU):c.-275T>C	rs567758523	0.00033

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