{{Rsnum
|rsid=17079928
|Chromosome=13
|position=24080089
|Orientation=plus
|GMAF=0.2576
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SPATA13
|Gene_s=SPATA13
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 6.2 | 47.3 | 46.4
| HCB | 0.7 | 25.5 | 73.7
| JPT | 0.0 | 27.4 | 72.6
| YRI | 4.8 | 35.4 | 59.9
| ASW | 15.8 | 35.1 | 49.1
| CHB | 0.7 | 25.5 | 73.7
| CHD | 0.0 | 17.0 | 83.0
| GIH | 0.0 | 18.8 | 81.2
| LWK | 10.2 | 39.8 | 50.0
| MEX | 3.5 | 52.6 | 43.9
| MKK | 12.3 | 40.6 | 47.1
| TSI | 9.3 | 46.4 | 44.3
| 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=1.3300
|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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}