Related gene-specific medical variations for Gene (Select 84693) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3247278	NC_000002.11:g.(?_71351316)_(71351693_?)dup	MCEE	Duplication	Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency	GLikely pathogenic
Select item 2689408	NM_032601.4(MCEE):c.275G>A (p.Gly92Glu)	MCEE (G92E)	Single nucleotide variant (missense variant)	Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency	GUncertain significance