{{Rsnum
|rsid=2074404
|Gene=WNT3
|Chromosome=17
|position=46788073
|Orientation=plus
|GMAF=0.348
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=WNT3
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 2.7 | 39.8 | 57.5
| HCB | 21.9 | 52.6 | 25.5
| JPT | 41.6 | 46.9 | 11.5
| YRI | 6.1 | 38.8 | 55.1
| ASW | 12.3 | 36.8 | 50.9
| CHB | 21.9 | 52.6 | 25.5
| CHD | 21.1 | 54.1 | 24.8
| GIH | 4.0 | 28.7 | 67.3
| LWK | 5.5 | 35.5 | 59.1
| MEX | 32.8 | 36.2 | 31.0
| MKK | 3.8 | 48.1 | 48.1
| TSI | 11.8 | 44.1 | 44.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20190752
|Trait=Celiac disease
|Title=Multiple common variants for celiac disease influencing immune gene expression
|RiskAllele=
|Pval=0.000001
|OR=1.11
|ORtxt=[1.06-1.16]
|OA=1
}}

{{PMID Auto
|PMID=24871462
|Title=Coeliac disease-associated polymorphisms influence thymic gene expression
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}