{{Rsnum
|rsid=10262453
|Gene=BBS9
|Chromosome=7
|position=33216427
|Orientation=plus
|GMAF=0.2075
|Gene_s=BBS9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 54.8 | 35.5 | 9.7
| HCB | 97.8 | 2.2 | 0.0
| JPT | 90.9 | 9.1 | 0.0
| YRI | 78.7 | 19.7 | 1.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 97.8 | 2.2 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23160099
  |Trait=Sagittal craniosynostosis
  |Title=A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.
  |RiskAllele=A
  |Pval=6E-20
  |OR=4.17
  |ORtxt=[3.13-5.88]
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}