{{Rsnum
|rsid=1873147
|Gene=IGKV2OR22-3
|Chromosome=15
|position=63020433
|Orientation=minus
|GMAF=0.4587
|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 | 4.4 | 33.6 | 61.9
| HCB | 75.2 | 22.6 | 2.2
| JPT | 71.7 | 27.4 | 0.9
| YRI | 19.7 | 51.7 | 28.6
| ASW | 14.0 | 52.6 | 33.3
| CHB | 75.2 | 22.6 | 2.2
| CHD | 78.0 | 19.3 | 2.8
| GIH | 25.7 | 51.5 | 22.8
| LWK | 16.5 | 54.1 | 29.4
| MEX | 10.3 | 46.6 | 43.1
| MKK | 14.7 | 57.7 | 27.6
| TSI | 5.9 | 33.3 | 60.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=23536526
|Title=Association and cumulative effects of GWAS-identified genetic variants for nonsyndromic orofacial clefts in a Chinese population
}}

{{PMID Auto GWAS
  |PMID=22863734
  |Trait=Orofacial clefts
  |Title=Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.
  |RiskAllele=C
  |Pval=8E-7
  |OR=1.43
  |ORtxt=[1.23-1.666]
  |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}}