{{Rsnum
|rsid=1884302
|Chromosome=20
|position=7125642
|Orientation=plus
|GMAF=0.4302
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.8 | 50.4 | 40.7
| HCB | 16.1 | 51.1 | 32.8
| JPT | 15.0 | 48.7 | 36.3
| YRI | 49.7 | 40.8 | 9.5
| ASW | 43.9 | 38.6 | 17.5
| CHB | 16.1 | 51.1 | 32.8
| CHD | 20.2 | 51.4 | 28.4
| GIH | 5.9 | 29.7 | 64.4
| LWK | 33.6 | 46.4 | 20.0
| MEX | 13.8 | 44.8 | 41.4
| MKK | 28.8 | 53.8 | 17.3
| TSI | 10.8 | 40.2 | 49.0
| 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=C
  |Pval=1E-39
  |OR=4.38
  |ORtxt=[3.51-5.45]
  |OA=1
}}

{{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}}