Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

MT-ND1

No public annotation

Chromosome
—
Cytoband
—
Variants (rsID)
160

MT-ND1 is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 160 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

13 reference-table entries with clinical significance.

  • rs199476120Benignsingle nucleotide variantParkinson disease, late-onset|Alzheimer disease|Leigh syndrome
  • rs28358582Benignsingle nucleotide variantCarcinoma of colon|SUDDEN INFANT DEATH SYNDROME|Leigh syndrome
  • rs28358585Benignsingle nucleotide variantLeigh syndrome
  • rs387906730Benignsingle nucleotide variantMitochondrial non-syndromic sensorineural hearing loss|Leigh syndrome
  • rs397515509Benignsingle nucleotide variantLeber optic atrophy|Leigh syndrome
  • rs41460449Conflicting interpretationssingle nucleotide variantLeber optic atrophy|Leigh syndrome
  • rs28357971Likely benignsingle nucleotide variant
  • rs374875201Likely benignsingle nucleotide variant
  • rs878853034Likely benignsingle nucleotide variant
  • rs397515507Likely pathogenicsingle nucleotide variantLeber optic atrophy|Mitochondrial disease
  • rs199476123Pathogenicsingle nucleotide variantJuvenile myopathy, encephalopathy, lactic acidosis AND stroke|Leigh syndrome|Leber optic atrophy
  • rs199476125Uncertain significancesingle nucleotide variantLeber optic atrophy|Mitochondrial disease
  • rs397515508Uncertain significancesingle nucleotide variantLeber optic atrophy|Optic neuropathy|Visual loss|Abnormal electroretinogram|Mitochondrial disease

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.