"GeneReviews"[submitter] AND "MT-ND6"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 65516	m.14279G>A	MT-ND6	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 65512	m.14325T>C	MT-ND6	Single nucleotide variant	Leigh syndrome	GBenign
Select item 9692	m.14453G>A	MT-ND6	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 9689	m.14459G>A	MT-ND6	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 65513	m.14482C>G	MT-ND6	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 9693	m.14482C>A	MT-ND6	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 9688	NC_012920.1:m.14484T>C	MT-ND6	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9694	m.14487T>C	MT-ND6	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9691	m.14495A>G	MT-ND6	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 65514	m.14498T>C	MT-ND6	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 65515	m.14568C>T	MT-ND6	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 9690	m.14596A>T	MT-ND6	Single nucleotide variant	Leber optic atrophy and dystonia	GPathogenic