ClinVar for MedGen (Select 1648371) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9715	m.10197G>A	MT-ND3	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9714	m.10158T>C	MT-ND3	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9712	m.10191T>C	MT-ND3	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database

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