C0917796[trait identifier] AND "Institute for Medical Genetics and Hum - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9641	NC_012920.1(MT-ATP6):m.8993T>G	MT-ATP6, MT-ATP8 +24 more	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9708	NC_012920.1(MT-ND4):m.11778G>A	MT-ND4	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 693767	NC_012920.1(MT-CYB):m.14795T>C	MT-CYB	Single nucleotide variant	Leber optic atrophy +1 more	GUncertain significance

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