C0342289[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9589	NC_012920.1:m.3243A>G	MT-TL1	Single nucleotide variant	Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1 +12 more	GPathogenic/Likely pathogenic
Select item 9584	m.8296A>G	MT-TK	Single nucleotide variant	Juvenile myopathy, encephalopathy, lactic acidosis AND stroke	GBenign
Select item 267298	NC_012920.1:m.14692A>G	MT-TE	Single nucleotide variant	Mitochondrial disease	GPathogenic
Select item 9617	m.14709T>C	MT-TE	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database

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