{{Rsnum
|rsid=10272438
|Gene=BBS9
|Chromosome=7
|position=33199222
|Orientation=plus
|GMAF=0.146
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=BBS9
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 53.6 | 37.5 | 8.9
| HCB | 96.3 | 3.7 | 0.0
| JPT | 84.8 | 14.3 | 0.9
| YRI | 100.0 | 0.0 | 0.0
| ASW | 91.2 | 8.8 | 0.0
| CHB | 96.3 | 3.7 | 0.0
| CHD | 98.2 | 1.8 | 0.0
| GIH | 85.0 | 14.0 | 1.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 63.8 | 27.6 | 8.6
| MKK | 87.8 | 11.5 | 0.6
| TSI | 61.4 | 32.7 | 5.9
| HapMapRevision=28
}}

{{PMID|18048322|OA=1
}} analysis of a published data set on [[age related macular degeneration]] revealed an unreported haplotype near [[rs10272438]] (P value = 0.0024).

{{PMID Auto
|PMID=15761122
|Title=Complement factor H polymorphism in age-related macular degeneration.
|OA=1
}}

{{PMID Auto
|PMID=18601744
|Title=Combining identity by descent and association in genetic case-control studies.
|OA=1
}}

{{PMID Auto
|PMID=19958499
|Title=A particle swarm based hybrid system for imbalanced medical data sampling.
|OA=1
}}

{{PMID Auto
|PMID=20181037
|Title=Incorporating prior knowledge to facilitate discoveries in a genome-wide association study on age-related macular degeneration.
|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 | Illumina Human 1M}}