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Gene entry

DNM2

dynamin 2

Chromosome
19
Cytoband
19p13.2
Variants (rsID)
35

DNM2 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 “dynamin 2”. The reference table lists 35 variants (rsID) for this gene.

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Clinically classified variants

15 reference-table entries with clinical significance.

  • rs147579870Benignsingle nucleotide variantAutosomal dominant centronuclear myopathy|Charcot-Marie-Tooth disease dominant intermediate B
  • rs3745674Benignsingle nucleotide variantAutosomal dominant centronuclear myopathy|Charcot-Marie-Tooth disease dominant intermediate B
  • rs121909093Conflicting interpretationssingle nucleotide variantAutosomal dominant Charcot-Marie-Tooth disease type 2M|Charcot-Marie-Tooth disease
  • rs144250390Conflicting interpretationssingle nucleotide variantPeripheral neuropathy|Charcot-Marie-Tooth disease dominant intermediate B|Autosomal dominant centronuclear myopathy
  • rs147026993Conflicting interpretationssingle nucleotide variantCentronuclear myopathy|Autosomal dominant centronuclear myopathy|Charcot-Marie-Tooth disease dominant intermediate B
  • rs200191870Conflicting interpretationssingle nucleotide variantAutosomal dominant centronuclear myopathy|Charcot-Marie-Tooth disease dominant intermediate B
  • rs201575500Conflicting interpretationssingle nucleotide variantAutosomal dominant centronuclear myopathy|Charcot-Marie-Tooth disease dominant intermediate B
  • rs201763720Conflicting interpretationssingle nucleotide variantCentronuclear myopathy|Charcot-Marie-Tooth disease dominant intermediate B
  • rs121909089Pathogenicsingle nucleotide variantAutosomal dominant centronuclear myopathy|Centronuclear myopathy|Charcot-Marie-Tooth disease dominant intermediate B
  • rs121909090Pathogenicsingle nucleotide variantAutosomal dominant centronuclear myopathy|Centronuclear myopathy|Charcot-Marie-Tooth disease dominant intermediate B|Charcot-Marie-Tooth disease
  • rs121909091Pathogenicsingle nucleotide variantAutosomal dominant centronuclear myopathy|Centronuclear myopathy|Charcot-Marie-Tooth disease dominant intermediate B|Abnormality of the musculature
  • rs121909092Pathogenicsingle nucleotide variantAutosomal dominant centronuclear myopathy|Centronuclear myopathy|Myopathy|Charcot-Marie-Tooth disease dominant intermediate B
  • rs267606772Pathogenicsingle nucleotide variantAutosomal dominant Charcot-Marie-Tooth disease type 2M|Charcot-Marie-Tooth disease dominant intermediate B
  • rs587783595Pathogenicsingle nucleotide variantCentronuclear myopathy|Charcot-Marie-Tooth disease dominant intermediate B|Autosomal dominant centronuclear myopathy|See cases
  • rs200408053Uncertain significancesingle nucleotide variantCharcot-Marie-Tooth disease dominant intermediate B

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.