Gene entry
KL
klotho
- Chromosome
- 13
- Cytoband
- 13q13.1
- Variants (rsID)
- 16
KL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q13.1). Its official name is “klotho”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs35328951Benignsingle nucleotide variantTumoral calcinosis, hyperphosphatemic, familial, 3
- rs3752472Benignsingle nucleotide variantTumoral calcinosis, hyperphosphatemic, familial, 3
- rs9536314Benignsingle nucleotide variantTumoral calcinosis, hyperphosphatemic, familial, 3
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.
