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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000303.3(PMM2):c.*368C>G	rs72766379	0.00580
NM_000303.3(PMM2):c.713G>A (p.Arg238His)	rs151319324	0.00035
NM_000303.3(PMM2):c.90C>G (p.Asp30Glu)	rs201556985	0.00019
NM_000303.3(PMM2):c.*10G>A	rs200930493	0.00015
NM_000303.3(PMM2):c.634A>G (p.Met212Val)	rs3743808	0.00014
NM_000303.3(PMM2):c.441C>T (p.Leu147=)	rs146990448	0.00010
NM_000303.3(PMM2):c.640-12G>A	rs375325546	0.00006
NM_000303.3(PMM2):c.738C>G (p.Ser246=)	rs373888957	0.00005
NM_000303.3(PMM2):c.639+10G>A	rs200593954	0.00004
NM_000303.3(PMM2):c.597C>T (p.Asp199=)	rs376412367	0.00003
NM_000303.3(PMM2):c.712C>T (p.Arg238Cys)	rs142459706	0.00003
NM_000303.3(PMM2):c.126A>G (p.Gly42=)	rs766984518	0.00001
NM_000303.3(PMM2):c.129G>A (p.Val43=)	rs777608895
NM_000303.3(PMM2):c.347+15A>C	rs751222355
NM_000303.3(PMM2):c.552T>C (p.Pro184=)	rs560182098

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