C0162671[trait identifier] AND "Kids Research, The Children's Hospital - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9589	NC_012920.1(MT-TL1):m.3243A>G	MT-TL1	Single nucleotide variant	Cerebral palsy +12 more	GPathogenic/Likely pathogenic
Select item 9617	NC_012920.1(MT-TE):m.14709T>C	MT-TE	Single nucleotide variant	Mitochondrial disease	GLikely pathogenic FDA Recognized database