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Gene entry

AHSG

alpha 2-HS glycoprotein

Chromosome
3
Cytoband
3q27.3
Variants (rsID)
3

AHSG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q27.3). Its official name is “alpha 2-HS glycoprotein”. The reference table lists 3 variants (rsID) for this gene.

Clinically classified variants

1 reference-table entries with clinical significance.

  • rs4917Benignsingle nucleotide variantLeanness, susceptibility to|Alopecia-intellectual disability syndrome 1

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.