{{Rsnum
|rsid=415430
|Gene=WNT3
|Chromosome=17
|position=46781778
|Orientation=minus
|GMAF=0.1253
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=WNT3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 62.8 | 36.3 | 0.9
| HCB | 100.0 | 0.0 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 79.6 | 20.4 | 0.0
| ASW | 73.7 | 22.8 | 3.5
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 84.2 | 13.9 | 2.0
| LWK | 85.5 | 13.6 | 0.9
| MEX | 74.1 | 20.7 | 5.2
| MKK | 76.9 | 20.5 | 2.6
| TSI | 52.9 | 36.3 | 10.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=21789800
|Title=[Analysis of single nucleotide polymorphism rs415430 in the WNT3 gene in the Russian population with the Parkinson disease]
}}

{{PMID Auto GWAS
|PMID=21812969
|Trait=None
|Title=Genome-Wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
|RiskAllele=T
|Pval=7E-7
|OR=None
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}