{{Rsnum
|rsid=16952065
|Gene=ITGA11
|Chromosome=15
|position=68426648
|Orientation=plus
|GMAF=0.04086
|Gene_s=ITGA11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 86.7 | 11.5 | 1.8
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 84.4 | 15.0 | 0.7
| ASW | 80.7 | 19.3 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 94.1 | 5.9 | 0.0
| LWK | 92.7 | 7.3 | 0.0
| MEX | 96.6 | 1.7 | 1.7
| MKK | 89.7 | 9.6 | 0.6
| TSI | 89.2 | 10.8 | 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=C
  |Pval=1E-6
  |OR=.44
  |ORtxt=[0.26-0.62] unit decrease
  |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}}