{{Rsnum
|rsid=3764628
|Gene=KLHL26
|Chromosome=19
|position=18636795
|Orientation=minus
|GMAF=0.09275
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=KLHL26
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 2.7 | 26.5 | 70.8
| HCB | 1.5 | 17.6 | 80.9
| JPT | 0.0 | 10.6 | 89.4
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 7.0 | 93.0
| CHB | 1.5 | 17.6 | 80.9
| CHD | 2.8 | 23.1 | 74.1
| GIH | 0.0 | 3.0 | 97.0
| LWK | 0.0 | 1.8 | 98.2
| MEX | 0.0 | 13.8 | 86.2
| MKK | 0.0 | 1.3 | 98.7
| TSI | 1.0 | 25.7 | 73.3
| 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=0.000004
|OR=1.8900
|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}}