List of variants in gene MME reported as uncertain significance for cerebellar disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_007289.4(MME):c.1040A>G (p.Tyr347Cys)	rs138218277	0.00064
NM_007289.4(MME):c.1706A>C (p.Gln569Pro)	rs1326179984	0.00001
NM_007289.4(MME):c.1735G>A (p.Gly579Ser)	rs767928746	0.00001
NM_007289.4(MME):c.1946T>G (p.Ile649Ser)	rs184666602

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