{{Rsnum
|rsid=2068361
|Gene=BMP6
|Chromosome=6
|position=7736510
|Orientation=minus
|GMAF=0.241
|Gene_s=BMP6
|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 | 4.4 | 27.4 | 68.1
| HCB | 5.1 | 29.9 | 65.0
| JPT | 5.3 | 48.7 | 46.0
| YRI | 7.5 | 35.4 | 57.1
| ASW | 8.8 | 31.6 | 59.6
| CHB | 5.1 | 29.9 | 65.0
| CHD | 12.8 | 31.2 | 56.0
| GIH | 2.0 | 22.8 | 75.2
| LWK | 2.7 | 24.5 | 72.7
| MEX | 6.9 | 39.7 | 53.4
| MKK | 4.5 | 40.4 | 55.1
| TSI | 13.7 | 40.2 | 46.1
| 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=1.6400
|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}}