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Gene entry

ITGA2

integrin subunit alpha 2

Chromosome
5
Cytoband
5q11.2
Variants (rsID)
29

ITGA2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q11.2). Its official name is “integrin subunit alpha 2”. The reference table lists 29 variants (rsID) for this gene.

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Clinically classified variants

9 reference-table entries with clinical significance.

  • rs1062535Benignsingle nucleotide variantPlatelet-type bleeding disorder 9
  • rs1109526Benignsingle nucleotide variantCombined molybdoflavoprotein enzyme deficiency|Platelet-type bleeding disorder 9
  • rs1126643Benignsingle nucleotide variantPlatelet-type bleeding disorder 9
  • rs116473481Benignsingle nucleotide variantPlatelet-type bleeding disorder 9
  • rs13173706Benignsingle nucleotide variantPlatelet-type bleeding disorder 9
  • rs1801106Benignsingle nucleotide variantPlatelet-type bleeding disorder 9
  • rs3212645Benignsingle nucleotide variantPlatelet-type bleeding disorder 9
  • rs3213805Benignsingle nucleotide variantPlatelet-type bleeding disorder 9
  • rs80331976Benignsingle nucleotide variantPlatelet-type bleeding disorder 9

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.