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Gene entry

KLHL3

kelch like family member 3

Chromosome
5
Cytoband
5q31.2
Variants (rsID)
21

KLHL3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q31.2). Its official name is “kelch like family member 3”. The reference table lists 21 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs17171525Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1|Pseudohypoaldosteronism type 2D
  • rs2301708Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1|Pseudohypoaldosteronism type 2D
  • rs3813314Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1|Pseudohypoaldosteronism type 2D
  • rs3813315Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1|Pseudohypoaldosteronism type 2D
  • rs7444370Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1|Pseudohypoaldosteronism type 2D

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.