"GeneReviews"[submitter] AND "MT-ND3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 430680	NC_012920.1(MT-TS2):m.8483_13459del	MT-ATP6, MT-ATP8 +10 more	Deletion	Mitochondrial disease	GPathogenic
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 9714	NC_012920.1(MT-ND3):m.10158T>C	MT-ND3	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9712	NC_012920.1(MT-ND3):m.10191T>C	MT-ND3	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 9715	NC_012920.1(MT-ND3):m.10197G>A	MT-ND3	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 65508	NC_012920.1(MT-ND3):m.10237T>C	MT-ND3	Single nucleotide variant	Leigh syndrome	GBenign
Select item 155887	NC_012920.1(MT-ND3):m.10254G>A	MT-ND3	Single nucleotide variant	Leigh syndrome	Gnot provided

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