List of variants in gene HGSNAT reported as uncertain significance 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)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_152419.3(HGSNAT):c.1237C>T (p.Pro413Ser)	rs201346206	0.00038
NM_152419.3(HGSNAT):c.1100_1103del	rs886062959
NM_152419.3(HGSNAT):c.*3044dup	rs886062965

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