{{Rsnum
|rsid=1329189
|Chromosome=10
|position=129998372
|Orientation=plus
|GMAF=0.3131
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 50.4 | 41.6 | 8.0
| HCB | 33.1 | 46.3 | 20.6
| JPT | 26.5 | 41.6 | 31.9
| YRI | 71.4 | 26.5 | 2.0
| ASW | 77.2 | 21.1 | 1.8
| CHB | 33.1 | 46.3 | 20.6
| CHD | 30.6 | 56.5 | 13.0
| GIH | 26.7 | 47.5 | 25.7
| LWK | 73.6 | 22.7 | 3.6
| MEX | 41.4 | 46.6 | 12.1
| MKK | 44.2 | 46.2 | 9.6
| TSI | 51.0 | 42.2 | 6.9
| 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=0.000005
|OR=1.3000
|ORtxt=None
|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}}