List of variants in gene MME reported as risk factor for Charcot-Marie-Tooth disease, axonal, type 2T

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: 3

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HGVS	dbSNP
NM_000902.4(MME):c.1265C>A (p.Ala422Asp)	rs777476150
NM_000902.4(MME):c.467del (p.Pro156fs)	rs749320057
NM_000902.4(MME):c.71G>A (p.Trp24Ter)	rs886039755

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