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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000263.4(NAGLU):c.1562C>T (p.Pro521Leu)	rs104894595	0.00003
NM_000263.4(NAGLU):c.1877G>A (p.Arg626Gln)	rs376545731	0.00003
NM_000263.4(NAGLU):c.1000G>A (p.Val334Ile)	rs749140168	0.00002
NM_000263.4(NAGLU):c.1772T>C (p.Leu591Pro)	rs1215582852	0.00001
NM_000263.4(NAGLU):c.1843C>T (p.Arg615Cys)	rs199729746	0.00001
NM_000263.4(NAGLU):c.608G>A (p.Arg203Gln)	rs904118831	0.00001
NM_000263.4(NAGLU):c.874G>A (p.Gly292Arg)	rs1358994052	0.00001
NM_000263.4(NAGLU):c.934G>A (p.Asp312Asn)	rs1052471595	0.00001
NM_000263.4(NAGLU):c.1212G>C (p.Trp404Cys)	rs777670507
NM_000263.4(NAGLU):c.2113G>A (p.Glu705Lys)	rs1364203992
NM_000263.4(NAGLU):c.461T>G (p.Ile154Arg)	rs770684838
NM_000263.4(NAGLU):c.680A>C (p.His227Pro)	rs747155746

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