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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.

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.