C0162672[trait identifier] AND "GeneReviews"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9574	m.611G>A	MT-TF	Single nucleotide variant	MERRF syndrome	GPathogenic
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 9591	m.3256C>T	MT-TL1	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 9590	m.3271T>C	MT-TL1	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9579	m.8344A>G	MT-TK	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9580	m.8356T>C	MT-TK	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 9585	m.8361G>A	MT-TK	Single nucleotide variant	MERRF syndrome	GPathogenic
Select item 9581	m.8363G>A	MT-TK	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database
Select item 9703	m.13042G>A	MT-ND5	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database

ClinVar