Gene entry
MT-ND4
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 105
MT-ND4 is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 105 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs200145866Benignsingle nucleotide variantLeber optic atrophy|Leigh syndrome
- rs200873900Benignsingle nucleotide variantLeber optic atrophy and dystonia|Leber optic atrophy|Leigh syndrome
- rs200911567Benignsingle nucleotide variantLeigh syndrome
- rs2853493Conflicting interpretationssingle nucleotide variantMitochondrial disease
- rs28718242Likely benignsingle nucleotide variant
- rs377109096Likely benignsingle nucleotide variant
- rs878853103Likely benignsingle nucleotide variant
- rs199476112Pathogenicsingle nucleotide variantLeber optic atrophy|Leber optic atrophy, susceptibility to|Mitochondrial disease
Other listed variants
- rs2853489
- rs2853490
- rs2853496
- rs2853498
- rs2853499
- rs2857285
- rs2857286
- rs3087901
- rs3088053
- rs3134800
- rs28358284
- rs28358285
- rs28358286
- rs28359168
- rs28359169
- rs28359170
- rs28359172
- rs28397767
- rs28411793
- rs28415973
- rs28433448
- rs28439211
- rs28469108
- rs28471078
- rs28493891
- rs28508189
- rs28524151
- rs28529320
- rs28550734
- rs28588421
- rs28592011
- rs28608480
- rs28609979
- rs28639786
- rs28669780
- rs28709525
- rs28713729
- rs28722520
- rs28756874
- rs28759201
- rs41445245
- rs55944643
- rs75214962
- rs118203889
- rs121434462
- rs121434463
- rs121434464
- rs121434473
- rs121434474
- rs193302938
- rs193302950
- rs200656196
- rs201027657
- rs201300253
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.