List of variants in gene MME reported as uncertain significance for Charcot-Marie-Tooth disease

Minimum submission review status:		Collection method:
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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.1272del (p.Arg425fs)	rs1060499935
NM_000902.4(MME):c.1904G>A (p.Gly635Asp)	rs151302020
NM_000902.4(MME):c.769C>A (p.Arg257Ser)	rs145687755

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