{{Rsnum
|rsid=3763558
|Gene=CPQ
|Chromosome=8
|position=96784503
|Orientation=plus
|GMAF=0.1474
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CPQ
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.9 | 23.9 | 75.2
| HCB | 0.0 | 12.4 | 87.6
| JPT | 0.9 | 18.6 | 80.5
| YRI | 13.7 | 52.1 | 34.2
| ASW | 5.3 | 38.6 | 56.1
| CHB | 0.0 | 12.4 | 87.6
| CHD | 0.0 | 7.3 | 92.7
| GIH | 0.0 | 21.8 | 78.2
| LWK | 9.3 | 45.4 | 45.4
| MEX | 1.8 | 7.0 | 91.2
| MKK | 6.5 | 35.1 | 58.4
| TSI | 1.0 | 18.6 | 80.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23725790
  |Trait=DNA methylation (variation)
  |Title=GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
  |RiskAllele=A
  |Pval=1E-6
  |OR=NR
  |ORtxt=NR
  }}

{{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}}