List of variants in gene MME reported as uncertain significance by Kariminejad - Najmabadi Pathology & Genetics Center

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	gnomAD frequency
NM_007289.4(MME):c.2242C>T (p.Arg748Trp)	rs141665432	0.00010
NM_007289.4(MME):c.1877A>G (p.Tyr626Cys)
NM_007289.4(MME):c.23T>G (p.Met8Arg)

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