List of variants in gene MME reported as uncertain significance by Revvity Omics, Revvity

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.860C>T (p.Thr287Met)	rs202094946	0.00004
NM_007289.4(MME):c.1590G>A (p.Val530=)	rs1209332250	0.00001
NM_007289.4(MME):c.1033G>C (p.Val345Leu)
NM_007289.4(MME):c.1526A>G (p.Glu509Gly)

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