Variants in gene NAGLU with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP
NM_000263.4(NAGLU):c.1900G>A (p.Glu634Lys)	rs147036053
NM_000263.4(NAGLU):c.274T>C (p.Tyr92His)	rs1555621454
NM_000263.4(NAGLU):c.874G>A (p.Gly292Arg)	rs1358994052
NM_000263.4(NAGLU):c.934G>A (p.Asp312Asn)	rs1052471595

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