Gene entry
CDH3
cadherin 3
- Chromosome
- 16
- Cytoband
- 16q22.1
- Variants (rsID)
- 15
CDH3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q22.1). Its official name is “cadherin 3”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs2296405Benignsingle nucleotide variantEEM syndrome|Congenital hypotrichosis with juvenile macular dystrophy
- rs35232945Benignsingle nucleotide variantEEM syndrome
- rs74026937Benignsingle nucleotide variantEEM syndrome
- rs34813787Conflicting interpretationssingle nucleotide variantEEM syndrome
- rs121434543Pathogenicsingle nucleotide variantEEM syndrome
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.