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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000303.3(PMM2):c.590A>C (p.Glu197Ala)	rs34258285	0.02088
NM_000303.3(PMM2):c.324G>A (p.Ala108=)	rs62031146	0.01239
NM_000303.3(PMM2):c.*17G>A	rs9936097	0.00905
NM_000303.3(PMM2):c.347+40G>A	rs142123453	0.00385
NM_000303.3(PMM2):c.110A>T (p.Gln37Leu)	rs2304472	0.00035
NM_000303.3(PMM2):c.366C>T (p.Phe122=)	rs145714866	0.00027
NM_000303.3(PMM2):c.90C>G (p.Asp30Glu)	rs201556985	0.00019
NM_000303.3(PMM2):c.634A>G (p.Met212Val)	rs3743808	0.00014
NM_000303.3(PMM2):c.712C>T (p.Arg238Cys)	rs142459706	0.00003
NM_000303.3(PMM2):c.640-28C>G	rs181837170

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