ClinVar for MedGen (Select 333240) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9733	m.3697G>A	MT-ND1	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 9715	NC_012920.1(MT-ND3):m.10197G>A	MT-ND3	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9710	NC_012920.1(MT-ND4):m.11696G>A	MT-ND4	Single nucleotide variant	Leigh syndrome	GBenign
Select item 9690	m.14596A>T	MT-ND6	Single nucleotide variant	Leber optic atrophy and dystonia	GPathogenic
Select item 9689	NC_012920.1(MT-ND6):m.14459G>A	MT-ND6	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database

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