Gene entry
MT-ND5
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 24
MT-ND5 is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
14 reference-table entries with clinical significance.
- rs201863060Benignsingle nucleotide variantLeber optic atrophy|Leigh syndrome
- rs28359185Benignsingle nucleotide variantLeigh syndrome
- rs386829190Benignsingle nucleotide variant
- rs386829198Benignsingle nucleotide variantLeigh syndrome
- rs879100848Benignsingle nucleotide variant
- rs199974018Conflicting interpretationssingle nucleotide variantLeber optic atrophy|Leigh syndrome
- rs2853499Conflicting interpretationssingle nucleotide variantMitochondrial disease
- rs55882959Conflicting interpretationssingle nucleotide variantLeigh syndrome
- rs28357668Likely benignsingle nucleotide variant
- rs28359176Likely benignsingle nucleotide variant
- rs57180882Likely benignsingle nucleotide variant
- rs267606898Likely pathogenicsingle nucleotide variantJuvenile myopathy, encephalopathy, lactic acidosis AND stroke|MERRF syndrome|Leigh syndrome due to mitochondrial complex I deficiency|Leber optic atrophy|Mitochondrial disease
- rs267606897Pathogenicsingle nucleotide variantLeigh syndrome due to mitochondrial complex I deficiency|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke|Leigh syndrome|Mitochondrial disease
- rs267606899Pathogenicsingle nucleotide variantLeber 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.