{{Rsnum
|rsid=7021663
|Gene=VAV2
|Chromosome=9
|position=133810892
|Orientation=plus
|GMAF=0.2328
|Gene_s=VAV2
|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 | 2.7 | 31.9 | 65.5
| HCB | 0.0 | 13.9 | 86.1
| JPT | 0.0 | 7.1 | 92.9
| YRI | 31.5 | 49.3 | 19.2
| ASW | 22.8 | 45.6 | 31.6
| CHB | 0.0 | 13.9 | 86.1
| CHD | 0.0 | 15.6 | 84.4
| GIH | 3.0 | 36.6 | 60.4
| LWK | 22.7 | 45.5 | 31.8
| MEX | 6.9 | 39.7 | 53.4
| MKK | 11.5 | 47.4 | 41.0
| TSI | 0.0 | 32.4 | 67.6
| 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=3E-6
  |OR=.18
  |ORtxt=[0.1-0.26] unit decrease
  |OA=1
}}

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