Gene entry
NDUFS2
NADH:ubiquinone oxidoreductase core subunit S2
- Chromosome
- 1
- Cytoband
- 1q23.3
- Variants (rsID)
- 16
NDUFS2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q23.3). Its official name is “NADH:ubiquinone oxidoreductase core subunit S2”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs11265565Benignsingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs121434429Conflicting interpretationssingle nucleotide variantMitochondrial complex 1 deficiency, nuclear type 6
- rs144937332Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs150667550Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency
- rs190184430Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs201554004Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs202121443Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs76309459Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs186476170Uncertain significancesingle nucleotide variant
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.