C0007758[trait identifier] AND "MGZ Medical Genetics Center"[submitter - 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 693064	NC_012920.1(MT-ATP6):m.9049G>A	MT-ATP6	Single nucleotide variant	Leigh syndrome +4 more	GLikely pathogenic
Select item 805947	NC_012920.1(MT-TE):m.14724G>A	MT-TE	Single nucleotide variant	Mitochondrial disease +4 more	GPathogenic

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