{{Rsnum
|rsid=2228467
|Gene=CCBP2
|Chromosome=3
|position=42864624
|Orientation=plus
|GMAF=0.02984
|Gene_s=CCBP2
|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 | 0.0 | 12.4 | 87.6
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 1.8 | 98.2
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 2.0 | 98.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 3.4 | 96.6
| MKK | 0.0 | 7.1 | 92.9
| TSI | 0.0 | 9.8 | 90.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23314186
  |Trait=Monocyte count
  |Title=Genetic variation associated with circulating monocyte count in the eMERGE Network.
  |RiskAllele=G
  |Pval=2E-7
  |OR=.30
  |ORtxt=unit increase
  |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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}