rs770306617

This variant is located in the NDUFS3 gene.

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ClinVar annotation

Conflicting Classifications
3 submitters1 publication

Mitochondrial complex I deficiency, nuclear type 1; Leigh syndrome; not specified; not provided

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About NDUFS3

This gene encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.[provided by RefSeq, Apr 2009]

View all NDUFS3 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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