{{Rsnum
|rsid=267196
|Gene=BMP6
|Chromosome=6
|position=7849102
|Orientation=plus
|GMAF=0.4555
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=BMP6
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 12.4 | 53.1 | 34.5
| HCB | 49.3 | 41.2 | 9.6
| JPT | 63.7 | 31.9 | 4.4
| YRI | 4.1 | 44.9 | 51.0
| ASW | 8.8 | 45.6 | 45.6
| CHB | 49.3 | 41.2 | 9.6
| CHD | 49.1 | 40.7 | 10.2
| GIH | 18.0 | 49.0 | 33.0
| LWK | 6.4 | 36.4 | 57.3
| MEX | 32.8 | 56.9 | 10.3
| MKK | 13.5 | 41.7 | 44.9
| TSI | 10.8 | 41.2 | 48.0
| HapMapRevision=28
}}

Part of a [[haplotype]] linked to [[stroke]] affecting perhaps 5% of [[sickle cell anemia]] patients

{{PMID Auto
|PMID=15784727
|Title=Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.
|OA=1
}}

{{PMID Auto
|PMID=18187665
|Title=Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.
|OA=1
}}

{{PMID Auto
|PMID=20401335
|Title=Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}