{{Rsnum
|rsid=2040862
|Gene=WNT8A
|Chromosome=5
|position=138084300
|Orientation=plus
|GMAF=0.08127
|Gene_s=WNT8A
|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 | 71.7 | 25.7 | 2.7
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 89.1 | 10.9 | 0.0
| ASW | 89.5 | 10.5 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 83.2 | 15.8 | 1.0
| LWK | 94.5 | 5.5 | 0.0
| MEX | 86.2 | 13.8 | 0.0
| MKK | 87.8 | 12.2 | 0.0
| TSI | 74.5 | 20.6 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22544366
|Trait=None
|Title=Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
|RiskAllele=T
|Pval=3E-7
|OR=1.1200
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=18413325
|Title=Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}