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.
