Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

ITGA2B

integrin subunit alpha 2b

Chromosome
17
Cytoband
17q21.31
Variants (rsID)
4

ITGA2B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q21.31). Its official name is “integrin subunit alpha 2b”. The reference table lists 4 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs143967758Benignsingle nucleotide variantGlanzmann thrombasthenia
  • rs76811038Uncertain significancesingle nucleotide variantGlanzmann thrombasthenia|Glanzmann thrombasthenia 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.