{{Rsnum
|rsid=17807815
|Gene=ATXN3
|Chromosome=14
|position=92089711
|Orientation=plus
|GMAF=0.07208
|Gene_s=ATXN3
|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 | 0.0 | 25.7 | 74.3
| HCB | 0.0 | 5.1 | 94.9
| JPT | 0.0 | 10.6 | 89.4
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 5.3 | 94.7
| CHB | 0.0 | 5.1 | 94.9
| CHD | 0.0 | 6.4 | 93.6
| GIH | 2.0 | 11.9 | 86.1
| LWK | 0.0 | 0.0 | 0.0
| MEX | 3.4 | 24.1 | 72.4
| MKK | 0.0 | 0.6 | 99.4
| TSI | 4.9 | 14.7 | 80.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22419666
|Trait=None
|Title=Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.
|RiskAllele=
|Pval=0.000006
|OR=2.3800
|ORtxt=None
|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 | Illumina Human 1M}}