Genetics University — Research, Education, Medical Genetics
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Gene entry

ENAM

enamelin

Chromosome
4
Cytoband
4q13.3
Variants (rsID)
8

ENAM is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q13.3). Its official name is “enamelin”. The reference table lists 8 variants (rsID) for this gene.

Clinically classified variants

3 reference-table entries with clinical significance.

  • rs3796704Benignsingle nucleotide variantAmelogenesis imperfecta
  • rs7671281Benignsingle nucleotide variantAmelogenesis imperfecta
  • rs143129444Uncertain significancesingle nucleotide variantAmelogenesis imperfecta

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.