{{Rsnum
|rsid=2933343
|Gene=ARHGAP11A
|Chromosome=3
|position=128939649
|Orientation=plus
|GMAF=0.3278
|Gene_s=ARHGAP11A
|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 | 4.6 | 24.6 | 70.8
| HCB | 24.4 | 55.6 | 20.0
| JPT | 25.0 | 50.0 | 25.0
| YRI | 4.8 | 49.2 | 46.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 24.4 | 55.6 | 20.0
| 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
}}{{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=8E-6
  |OR=.16
  |ORtxt=[0.091-0.232] unit decrease
  |OA=1
}}