{{Rsnum
|rsid = 235330
|geno1 = (A;A)
|geno2 = (A;T)
|geno3 = (T;T)
|Gene = ITGB2
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=T
|Chromosome=21
|position=44894992
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ITGB2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=235330
|allele=A
|frequency=1
|uid=1103643132963
|type=homozygous_SNP
|hugo=ITGB2
|ensembl gene=ENSG00000160255
|ensembl transcript=ENST00000302347
|sift=
|disease=Defects in ITGB2 are the cause of leukocyte adhesion deficiency type I (LAD1) (MIM:116920). LAD1 patients have recurrent bacterial infections and their leukocytes are deficient in a wide range of adhesion-dependent functions.
}}

{{GET Evidence
|gene=ITGB2
|aa_change=Gln354His
|aa_change_short=Q354H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs235330
|overall_frequency_n=10757
|overall_frequency_d=10758
|overall_frequency=0.999907
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=112
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.543
|genetests_testable=Y
|nblosum100=-1
|autoscore=2
|n_web_uneval=1
}}
{{on chip | HumanOmni1Quad}}