"GeneReviews"[submitter] AND "MT-ND2"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9734	NC_012920.1(MT-ND1):m.3946G>A	MT-ATP6, MT-ATP8 +20 more	Single nucleotide variant	Leigh syndrome +2 more	GPathogenic/Likely pathogenic
Select item 9718	NC_012920.1(MT-ND2):m.4640C>A	MT-ND2	Single nucleotide variant	Leigh syndrome	GBenign
Select item 9721	NC_012920.1(MT-ND2):m.4681T>C	MT-ND2	Single nucleotide variant	Leigh syndrome due to mitochondrial complex I deficiency	GPathogenic
Select item 9717	m.5244G>A	MT-ND2	Single nucleotide variant	Mitochondrial disease	GUncertain significanceFDA Recognized database
Select item 9641	NC_012920.1(MT-ATP6):m.8993T>G	MT-ATP6, MT-ATP8 +24 more	Single nucleotide variant	Mitochondrial disease	GPathogenicFDA Recognized database

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