Gene entry
MT-ND2
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 5
MT-ND2 is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 5 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs28357980Benignsingle nucleotide variantLeber optic atrophy|Leigh syndrome
- rs3021086Benignsingle nucleotide variantMitochondrial disease
- rs3902405Benignsingle nucleotide variant
- rs878853072Likely benignsingle nucleotide variant
- rs267606888Pathogenicsingle nucleotide variantMitochondrial complex I deficiency
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.