Gene entry
CHGB
chromogranin B
- Chromosome
- 20
- Cytoband
- 20p12.3
- Variants (rsID)
- 9
CHGB is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p12.3). Its official name is “chromogranin B”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
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.