List of variants in gene MME reported as likely benign for cerebellar ataxia

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_007289.4(MME):c.2133G>A (p.Val711=)	rs61760409	0.00518
NM_007289.4(MME):c.1255A>C (p.Met419Leu)	rs34931605	0.00459

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