Gene entry
KLHL7
kelch like family member 7
- Chromosome
- 7
- Cytoband
- 7p15.3
- Variants (rsID)
- 9
KLHL7 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7p15.3). Its official name is “kelch like family member 7”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs137853113Pathogenicsingle nucleotide variantRetinitis pigmentosa 42|Retinitis pigmentosa|Retinal dystrophy
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.