List of variants in gene NAGLU reported as pathogenic by Centogene AG - the Rare Disease Company

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_000263.4(NAGLU):c.1336G>A (p.Glu446Lys)	rs114625063
NM_000263.4(NAGLU):c.291T>G (p.Cys97Trp)	rs2092906798
NM_000263.4(NAGLU):c.701G>C (p.Arg234Pro)	rs886042073

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