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Gene entry

NF2

NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor

Chromosome
22
Cytoband
22q12.2
Variants (rsID)
51

NF2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q12.2). Its official name is “NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor”. The reference table lists 51 variants (rsID) for this gene.

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Clinically classified variants

28 reference-table entries with clinical significance.

  • rs41278851Benignsingle nucleotide variantNeurofibromatosis, type 2
  • rs141629512Conflicting interpretationssingle nucleotide variantNeurofibromatosis, type 2|Hereditary cancer-predisposing syndrome
  • rs145666157Conflicting interpretationssingle nucleotide variantNeurofibromatosis, type 2|Hereditary cancer-predisposing syndrome
  • rs1060503666Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs1060503667Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs1060503670Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs1064796632Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs121434259Pathogenicsingle nucleotide variantMeningioma|Neurofibromatosis, type 2
  • rs121434261Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs587776562Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs587776563PathogenicDeletionMeningioma
  • rs587776564PathogenicInsertionSchwannomatosis 1
  • rs587776565PathogenicDeletionSchwannomatosis 1
  • rs74315492Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs74315493Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs74315494Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs74315495Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs74315496Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs74315497Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs74315499Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs74315501Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs74315503Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs74315504Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs74315505Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs794728682Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs878853925Pathogenicsingle nucleotide variantNeurofibromatosis, type 2
  • rs1480040681Uncertain significancesingle nucleotide variantNeurofibromatosis, type 2
  • rs752963731Uncertain significancesingle nucleotide variantNeurofibromatosis, type 2

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.