Gene entry
ITGB2
integrin subunit beta 2
- Chromosome
- 21
- Cytoband
- 21q22.3
- Variants (rsID)
- 34
ITGB2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 21 (region 21q22.3). Its official name is “integrin subunit beta 2”. The reference table lists 34 variants (rsID) for this gene.
Clinically classified variants
13 reference-table entries with clinical significance.
- rs11088969Benignsingle nucleotide variantLeukocyte adhesion deficiency 1
- rs2230531Benignsingle nucleotide variantLeukocyte adhesion deficiency 1
- rs235330Benignsingle nucleotide variantLeukocyte adhesion deficiency 1
- rs5030670Benignsingle nucleotide variantLeukocyte adhesion deficiency 1
- rs5030672Benignsingle nucleotide variantLeukocyte adhesion deficiency 1
- rs9983887Benignsingle nucleotide variantLeukocyte adhesion deficiency 1
- rs137959302Conflicting interpretationssingle nucleotide variantLeukocyte adhesion deficiency 1
- rs138682103Conflicting interpretationssingle nucleotide variantLeukocyte adhesion deficiency 1
- rs137852614Pathogenicsingle nucleotide variantLeukocyte adhesion deficiency 1
- rs137852616Pathogenicsingle nucleotide variantLeukocyte adhesion deficiency 1|Inborn genetic diseases
- rs137852618Pathogenicsingle nucleotide variantLeukocyte adhesion deficiency 1
- rs201752283Pathogenicsingle nucleotide variantLeukocyte adhesion deficiency 1
- rs148031841Uncertain significancesingle nucleotide variantLeukocyte adhesion deficiency 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.