Gene entry
LRIT3
leucine rich repeat, Ig-like and transmembrane domains 3
- Chromosome
- 4
- Cytoband
- 4q25
- Variants (rsID)
- 8
LRIT3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q25). Its official name is “leucine rich repeat, Ig-like and transmembrane domains 3”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs17040904Benignsingle nucleotide variantCongenital Stationary Night Blindness, Recessive
- rs4698797Benignsingle nucleotide variantCongenital Stationary Night Blindness, Recessive|Congenital stationary night blindness 1F
- rs35997283Likely benignsingle nucleotide variant
- rs376610215Pathogenicsingle nucleotide variantCongenital stationary night blindness 1F
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.