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.
