List of variants in gene MPZ reported as likely benign for Charcot-Marie-Tooth disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000530.8(MPZ):c.504G>A (p.Val168=)	rs145592910	0.00074
NM_000530.8(MPZ):c.24C>T (p.Ser8=)	rs144841836	0.00037
NM_000530.8(MPZ):c.*1C>T	rs751066172	0.00001
NM_000530.8(MPZ):c.174C>T (p.Val58=)	rs753575261	0.00001
NM_000530.8(MPZ):c.531C>T (p.Tyr177=)	rs779159258	0.00001
NM_000530.8(MPZ):c.42G>A (p.Leu14=)	rs1670359930
NM_000530.8(MPZ):c.645+10A>G	rs1670232533

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