Variants in gene MPZ 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000530.8(MPZ):c.133C>T (p.Arg45Trp)	rs200151353	0.00051
NM_000530.8(MPZ):c.637G>C (p.Gly213Arg)	rs202176679	0.00005
NM_000530.8(MPZ):c.211G>A (p.Glu71Lys)	rs573007540	0.00004
NM_000530.8(MPZ):c.200G>A (p.Arg67His)	rs201720099	0.00001
NM_000530.8(MPZ):c.271G>A (p.Glu91Lys)	rs1383238492
NM_000530.8(MPZ):c.585-7_585-5del	rs770501358
NM_000530.8(MPZ):c.646-7C>G	rs377495735

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