{{Rsnum
|rsid=4703822
|Gene=RASGRF2
|Chromosome=5
|position=81115402
|Orientation=plus
|GMAF=0.2635
|Gene_s=RASGRF2
|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 | 11.5 | 46.9 | 41.6
| HCB | 4.4 | 38.7 | 56.9
| JPT | 15.0 | 55.8 | 29.2
| YRI | 1.4 | 25.9 | 72.8
| ASW | 1.8 | 19.3 | 78.9
| CHB | 4.4 | 38.7 | 56.9
| CHD | 3.7 | 38.5 | 57.8
| GIH | 4.0 | 49.5 | 46.5
| LWK | 0.0 | 30.0 | 70.0
| MEX | 5.2 | 37.9 | 56.9
| MKK | 9.6 | 44.2 | 46.2
| TSI | 13.7 | 47.1 | 39.2
| 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=1.5900
|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}}
{{on chip | NatGeo2}}