Gene entry
MT-ND6
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 13
MT-ND6 is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs397515505Benignsingle nucleotide variantLeber optic atrophy|Leigh syndrome
- rs3135030Likely benignsingle nucleotide variant
- rs199476106Likely pathogenicsingle nucleotide variantLeber optic atrophy|Mitochondrial disease
- rs199476107Likely pathogenicsingle nucleotide variantJuvenile myopathy, encephalopathy, lactic acidosis AND stroke|Leigh syndrome|Mitochondrial disease
- rs397515506Likely pathogenicsingle nucleotide variantLeber optic atrophy|Mitochondrial disease
- rs199476104Pathogenicsingle nucleotide variantLeber optic atrophy|Leigh syndrome
- rs199476109Pathogenicsingle nucleotide variantLeigh syndrome due to mitochondrial complex I deficiency|Striatal necrosis, bilateral, with dystonia|Leigh syndrome|Leber optic atrophy
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.