Variants in gene MPZ 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000530.8(MPZ):c.684C>T (p.Ser228=)	rs34307129	0.01960
NM_000530.8(MPZ):c.24C>T (p.Ser8=)	rs144841836	0.00037
NM_000530.8(MPZ):c.51G>A (p.Leu17=)	rs149637045	0.00019

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