Variants in gene PMM2 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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	gnomAD frequency
NM_000303.3(PMM2):c.90C>G (p.Asp30Glu)	rs201556985	0.00019
NM_000303.3(PMM2):c.441C>T (p.Leu147=)	rs146990448	0.00010
NM_000303.3(PMM2):c.712C>T (p.Arg238Cys)	rs142459706	0.00003
NM_000303.3(PMM2):c.93C>T (p.Phe31=)	rs61730638

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