{{Rsnum
|rsid=2860223
|Chromosome=8
|position=133656434
|Orientation=plus
|GMAF=0.3274
|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 | 45.1 | 43.4 | 11.5
| HCB | 31.4 | 49.6 | 19.0
| JPT | 36.3 | 50.4 | 13.3
| YRI | 55.8 | 40.1 | 4.1
| ASW | 54.4 | 36.8 | 8.8
| CHB | 31.4 | 49.6 | 19.0
| CHD | 30.8 | 48.6 | 20.6
| GIH | 25.7 | 52.5 | 21.8
| LWK | 64.5 | 33.6 | 1.8
| MEX | 29.3 | 51.7 | 19.0
| MKK | 61.9 | 33.5 | 4.5
| TSI | 52.0 | 37.3 | 10.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382809
  |Trait=Schizophrenia (negative symptoms)
  |Title=BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies.
  |RiskAllele=C
  |Pval=2E-6
  |OR=1.26
  |ORtxt=[NR]
  |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}}