Gene entry
MT-TI
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 6
MT-TI is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 6 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs121434465Benignsingle nucleotide variantCardiomyopathy, fatal infantile|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
- rs121434467Conflicting interpretationssingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Mitochondrial non-syndromic sensorineural hearing loss|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
- rs121434468Conflicting interpretationssingle nucleotide variantMultisystem disorder|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke|MERRF syndrome
- rs121434470Likely pathogenicsingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Primary dilated cardiomyopathy|Asymmetric septal hypertrophy|MERRF syndrome|Mitochondrial disease
- rs121434471Pathogenicsingle nucleotide variantHypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial
- rs121434469Uncertain significancesingle nucleotide variantEncephalopathy, familial progressive necrotizing|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.