Gene entry
LRAT
lecithin retinol acyltransferase
- Chromosome
- 4
- Cytoband
- 4q32.1
- Variants (rsID)
- 4
LRAT is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q32.1). Its official name is “lecithin retinol acyltransferase”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs17032000Benignsingle nucleotide variantRetinitis pigmentosa|Leber congenital amaurosis|Leber congenital amaurosis 14
- rs75368761Benignsingle nucleotide variantRetinitis pigmentosa|Leber congenital amaurosis 14
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.