{{Rsnum
|rsid=3006564
|Chromosome=10
|position=30177888
|Orientation=plus
|GMAF=0.4376
|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 | 39.8 | 47.8 | 12.4
| HCB | 12.4 | 42.3 | 45.3
| JPT | 27.4 | 43.4 | 29.2
| YRI | 57.1 | 36.1 | 6.8
| ASW | 56.1 | 38.6 | 5.3
| CHB | 12.4 | 42.3 | 45.3
| CHD | 17.4 | 35.8 | 46.8
| GIH | 19.8 | 51.5 | 28.7
| LWK | 50.9 | 38.2 | 10.9
| MEX | 32.8 | 50.0 | 17.2
| MKK | 42.3 | 43.6 | 14.1
| TSI | 22.5 | 51.0 | 26.5
| 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=0.000005
|OR=1.3200
|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}}