Gene entry
MT-TW
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 3
MT-TW is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs199474673Likely pathogenicsingle nucleotide variantInborn mitochondrial myopathy|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke|Mitochondrial disease
- rs199474671Pathogenicsingle nucleotide variantMitochondrial encephalopathy
- rs199474674Pathogenicsingle nucleotide variantNeurogastrointestinal syndrome, mitochondrial|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.