Gene entry
LCA5
lebercilin LCA5
- Chromosome
- 6
- Cytoband
- 6q14.1
- Variants (rsID)
- 13
LCA5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q14.1). Its official name is “lebercilin LCA5”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs2655655Benignsingle nucleotide variantLeber congenital amaurosis 5|Leber congenital amaurosis 1
- rs121918165Pathogenicsingle nucleotide variantLeber congenital amaurosis 5|Inborn genetic diseases|Leber congenital amaurosis|Retinal dystrophy
- rs9343917Uncertain significancesingle nucleotide variantLeber congenital amaurosis 5
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.