Gene entry
MT-ND3
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 38
MT-ND3 is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 38 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs193302928Benignsingle nucleotide variantLeigh syndrome
- rs2853826Benignsingle nucleotide variantParkinson disease, resistance to|Leigh syndrome
- rs41487950Benignsingle nucleotide variantLeigh syndrome
- rs199476117Pathogenicsingle nucleotide variantMitochondrial complex 1 deficiency, mitochondrial type 1|Leigh syndrome|Mitochondrial disease
- rs267606890Pathogenicsingle nucleotide variantMitochondrial complex 1 deficiency, mitochondrial type 1|Leigh syndrome|Mitochondrial complex I deficiency|Mitochondrial disease
- rs267606891Pathogenicsingle nucleotide variantLeber optic atrophy and dystonia|Mitochondrial complex 1 deficiency, mitochondrial type 1|Leigh syndrome|Mitochondrial DNA-Associated Leigh Syndrome and NARP|Mitochondrial disease
Other listed variants
- rs2853487
- rs2853488
- rs28358280
- rs28358281
- rs28358283
- rs28437034
- rs28488153
- rs28520241
- rs28532736
- rs28645634
- rs28709356
- rs28735641
- rs193302933
- rs199688733
- rs200487531
- rs370873805
- rs372025447
- rs372297272
- rs375360074
- rs386419955
- rs386419971
- rs386829102
- rs386829103
- rs386829104
- rs386829109
- rs386829110
- rs386829113
- rs869087443
- rs869201226
- rs879012922
- rs879015842
- rs879139020
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.