Gene entry
HELB
DNA helicase B
- Chromosome
- 12
- Cytoband
- 12q14.3|12q
- Variants (rsID)
- 11
HELB is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q14.3|12q). Its official name is “DNA helicase B”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs4430553Not classifiedmissense_variant
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.
