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Gene entry

ITGB3

integrin subunit beta 3

Chromosome
17
Cytoband
17q21.32
Variants (rsID)
34

ITGB3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q21.32). Its official name is “integrin subunit beta 3”. The reference table lists 34 variants (rsID) for this gene.

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Clinically classified variants

9 reference-table entries with clinical significance.

  • rs17225109Benignsingle nucleotide variantGlanzmann thrombasthenia
  • rs2317676Benignsingle nucleotide variantGlanzmann thrombasthenia
  • rs4642Benignsingle nucleotide variantGlanzmann thrombasthenia
  • rs5918Benignsingle nucleotide variantPL(A1)/(A2) ALLOANTIGEN POLYMORPHISM|Glanzmann thrombasthenia|Myocardial infarction, susceptibility to
  • rs5919Benignsingle nucleotide variantGlanzmann thrombasthenia
  • rs121918446Likely pathogenicsingle nucleotide variantGlanzmann thrombasthenia 2|Glanzmann thrombasthenia|Glanzmann thrombasthenia 1
  • rs121918452Likely pathogenicsingle nucleotide variantGlanzmann thrombasthenia 2|Glanzmann thrombasthenia
  • rs121918448Uncertain significancesingle nucleotide variantMo ALLOANTIGEN POLYMORPHISM
  • rs138729147Uncertain significancesingle nucleotide variantGlanzmann thrombasthenia

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.