{{Rsnum
|rsid=17724206
|Gene=BBS9
|Chromosome=7
|position=33384149
|Orientation=plus
|GMAF=0.1653
|Gene_s=BBS9
|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 | 8.0 | 41.6 | 50.4
| HCB | 0.0 | 3.6 | 96.4
| JPT | 0.9 | 15.9 | 83.2
| YRI | 0.0 | 14.3 | 85.7
| ASW | 0.0 | 14.0 | 86.0
| CHB | 0.0 | 3.6 | 96.4
| CHD | 0.0 | 2.8 | 97.2
| GIH | 1.0 | 22.8 | 76.2
| LWK | 0.0 | 12.7 | 87.3
| MEX | 12.1 | 36.2 | 51.7
| MKK | 1.9 | 24.4 | 73.7
| TSI | 6.9 | 38.2 | 54.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=23160099
|Title=A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}