{{Rsnum
|rsid=17138064
|Chromosome=17
|position=36831827
|Orientation=plus
|GMAF=0.08678
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 17.7 | 81.4
| HCB | 4.4 | 27.7 | 67.9
| JPT | 2.7 | 22.1 | 75.2
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 5.3 | 94.7
| CHB | 4.4 | 27.7 | 67.9
| CHD | 1.8 | 33.9 | 64.2
| GIH | 1.0 | 14.9 | 84.2
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 17.2 | 82.8
| MKK | 0.0 | 0.0 | 0.0
| TSI | 1.0 | 13.7 | 85.3
| 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=5E-7
|OR=1.9200
|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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}