"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[s - ClinVar - NCBI

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Items: 4

	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 523307	NC_012920.1(MT-CO3):m.9355A>T	MT-CO3	Single nucleotide variant	Exercise intolerance +12 more	GUncertain significance
Select item 693181	NC_012920.1(MT-CO3):m.9549C>T	MT-CO3	Single nucleotide variant	Leigh syndrome +1 more	GUncertain significance
Select item 9652	NC_012920.1(MT-CO3):m.9804G>A	MT-CO3	Single nucleotide variant	not specified +4 more	GConflicting classifications of pathogenicity

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