ClinVar for MedGen (Select 433159) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 693604	NC_012920.1(MT-ND5):m.13763C>T	MT-ND5	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 693347	NC_012920.1(MT-ND4):m.11150G>A	MT-ND4	Single nucleotide variant	Leigh syndrome	GBenign
Select item 693041	NC_012920.1(MT-ATP6):m.8975T>C	MT-ATP6	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 585120	NC_012920.1(MT-ATP6):m.8686T>C	MT-ATP6	Single nucleotide variant	Leigh syndrome	GUncertain significance
Select item 9715	NC_012920.1(MT-ND3):m.10197G>A	MT-ND3	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9647	NC_012920.1(MT-ATP6):m.9185T>C	MT-ATP6	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database

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