Gene entry
RANBP2
RAN binding protein 2
- Chromosome
- 2
- Cytoband
- 2q13
- Variants (rsID)
- 7
RANBP2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q13). Its official name is “RAN binding protein 2”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs140280672Benignsingle nucleotide variantFamilial acute necrotizing encephalopathy
- rs145886643Benignsingle nucleotide variantFamilial acute necrotizing encephalopathy
- rs112835359Conflicting interpretationssingle nucleotide variantFamilial acute necrotizing encephalopathy
- rs142231499Likely benignsingle nucleotide variantFamilial acute necrotizing encephalopathy
- rs200328905Uncertain significancesingle nucleotide variantFamilial acute necrotizing encephalopathy
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.