Genetics University — Research, Education, Medical Genetics
Knowledge Hub

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.