{{Rsnum
|rsid=2503875
|Chromosome=10
|position=43814049
|Orientation=plus
|GMAF=0.286
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 10.6 | 42.5 | 46.9
| HCB | 23.5 | 41.7 | 34.8
| JPT | 22.0 | 54.1 | 23.9
| YRI | 0.0 | 1.4 | 98.6
| ASW | 1.8 | 8.8 | 89.5
| CHB | 23.5 | 41.7 | 34.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 21.0 | 52.0 | 27.0
| LWK | 0.0 | 8.3 | 91.7
| MEX | 8.6 | 51.7 | 39.7
| MKK | 0.6 | 14.2 | 85.2
| TSI | 11.9 | 39.6 | 48.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20598377
|Trait=Multiple sclerosis
|Title=Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis
|RiskAllele=A
|Pval=2E-7
|OR=1.66
|ORtxt=[1.37-2.00]
}}

{{PMID Auto
|PMID=20532249
|Title=Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}