{{Rsnum
|rsid=2317385
|Gene=ITGB3
|Chromosome=17
|position=47252316
|Orientation=minus
|GMAF=0.303
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ITGB3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 66.4 | 30.1 | 3.5
| HCB | 23.4 | 56.9 | 19.7
| JPT | 39.8 | 49.6 | 10.6
| YRI | 31.5 | 50.7 | 17.8
| ASW | 45.6 | 47.4 | 7.0
| CHB | 23.4 | 56.9 | 19.7
| CHD | 22.2 | 51.9 | 25.9
| GIH | 52.5 | 39.6 | 7.9
| LWK | 34.9 | 47.7 | 17.4
| MEX | 70.7 | 25.9 | 3.4
| MKK | 36.8 | 45.2 | 18.1
| TSI | 55.9 | 37.3 | 6.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=21102624
|Title=Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes
|OA=1
}}

{{PMID Auto
|PMID=17827388
|Title=Genetic variation in 1253 immune and inflammation genes and risk of non-Hodgkin lymphoma.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}