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Gene entry

KLHL41

kelch like family member 41

Chromosome
2
Cytoband
2q31.1
Variants (rsID)
12

KLHL41 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q31.1). Its official name is “kelch like family member 41”. The reference table lists 12 variants (rsID) for this gene.

Clinically classified variants

5 reference-table entries with clinical significance.

  • rs139415849Benignsingle nucleotide variantNemaline myopathy 9
  • rs147527225Benignsingle nucleotide variantNemaline myopathy 9
  • rs28730867Benignsingle nucleotide variantNemaline myopathy 9
  • rs28763868Benignsingle nucleotide variantNemaline myopathy 9
  • rs34623017Benignsingle nucleotide variantNemaline myopathy 9

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.