Gene entry
RTN2
reticulon 2
- Chromosome
- 19
- Cytoband
- 19q13.32
- Variants (rsID)
- 4
RTN2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.32). Its official name is “reticulon 2”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs143937661Benignsingle nucleotide variantSpastic paraplegia, autosomal dominant|Spastic paraplegia|Hereditary spastic paraplegia
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.