{{Rsnum
|rsid=11228719
|Chromosome=11
|position=56672760
|Orientation=plus
|GMAF=0.377
|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 | 15.9 | 30.2 | 54.0
| HCB | 3.7 | 34.1 | 62.2
| JPT | 0.9 | 38.9 | 60.2
| YRI | 54.1 | 38.4 | 7.5
| ASW | 28.1 | 59.6 | 12.3
| CHB | 3.7 | 34.1 | 62.2
| CHD | 0.9 | 30.3 | 68.8
| GIH | 10.9 | 30.7 | 58.4
| LWK | 57.3 | 37.3 | 5.5
| MEX | 10.3 | 24.1 | 65.5
| MKK | 34.8 | 54.2 | 11.0
| TSI | 15.8 | 36.6 | 47.5
| 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=0.000004
|OR=1.6400
|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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}