Gene entry
CLDN19
claudin 19
- Chromosome
- 1
- Cytoband
- 1p34.2
- Variants (rsID)
- 7
CLDN19 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p34.2). Its official name is “claudin 19”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs116804195Benignsingle nucleotide variantRenal hypomagnesemia 5 with ocular involvement
- rs12065961Benignsingle nucleotide variantRenal hypomagnesemia 5 with ocular involvement
- rs4660658Benignsingle nucleotide variantRenal hypomagnesemia 5 with ocular involvement
- rs9660973Benignsingle nucleotide variantRenal hypomagnesemia 5 with ocular involvement
- rs140913043Uncertain significancesingle nucleotide variantRenal hypomagnesemia 5 with ocular involvement
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.