Gene entry
CLDN16
claudin 16
- Chromosome
- 3
- Cytoband
- 3q28
- Variants (rsID)
- 31
CLDN16 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q28). Its official name is “claudin 16”. The reference table lists 31 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs35041121Benignsingle nucleotide variantPrimary hypomagnesemia
- rs104893721Pathogenicsingle nucleotide variantPrimary hypomagnesemia
- rs104893729Pathogenicsingle nucleotide variantPrimary hypomagnesemia
- rs104893731Pathogenicsingle nucleotide variantPrimary hypomagnesemia
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.
