{{Rsnum
|rsid=7209700
|Gene=ITGB3
|Chromosome=17
|position=47273752
|Orientation=plus
|GMAF=0.3503
|Gene_s=ITGB3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 42.3 | 48.6 | 9.0
| HCB | 42.1 | 45.9 | 12.0
| JPT | 45.4 | 41.7 | 13.0
| YRI | 25.9 | 47.6 | 26.6
| ASW | 42.9 | 44.6 | 12.5
| CHB | 42.1 | 45.9 | 12.0
| CHD | 34.3 | 46.7 | 19.0
| GIH | 37.6 | 51.5 | 10.9
| 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
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=G
  |Pval=4E-7
  |OR=.17
  |ORtxt=[0.1-0.23] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}