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Gene entry

DNMT1

DNA methyltransferase 1

Chromosome
19
Cytoband
19p13.2
Variants (rsID)
19

DNMT1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19p13.2). Its official name is “DNA methyltransferase 1”. The reference table lists 19 variants (rsID) for this gene.

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Clinically classified variants

12 reference-table entries with clinical significance.

  • rs150999369Benignsingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome
  • rs201213597Benignsingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome
  • rs2228611Benignsingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome|Autosomal dominant cerebellar ataxia, deafness and narcolepsy
  • rs369373339Benignsingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome
  • rs61750053Benignsingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome
  • rs138841970Conflicting interpretationssingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome|Beckwith-Wiedemann syndrome
  • rs146112081Conflicting interpretationssingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome
  • rs539948794Conflicting interpretationssingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome
  • rs62621089Conflicting interpretationssingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome
  • rs753248212Conflicting interpretationssingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome
  • rs769623856Conflicting interpretationssingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome
  • rs199473692Pathogenicsingle nucleotide variantHereditary sensory neuropathy-deafness-dementia syndrome

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.