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Gene entry

NGF

nerve growth factor

Chromosome
1
Cytoband
1p13.2
Variants (rsID)
31

NGF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p13.2). Its official name is “nerve growth factor”. The reference table lists 31 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs11102930Benignsingle nucleotide variant
  • rs11466110Benignsingle nucleotide variantCongenital sensory neuropathy with selective loss of small myelinated fibers
  • rs11466111Benignsingle nucleotide variantCongenital sensory neuropathy with selective loss of small myelinated fibers
  • rs6330Benignsingle nucleotide variantCongenital sensory neuropathy with selective loss of small myelinated fibers
  • rs11466112Pathogenicsingle nucleotide variantCongenital sensory neuropathy with selective loss of small myelinated fibers

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.