{{Rsnum
|rsid=4629710
|Gene=AKAP7
|Chromosome=6
|position=131242437
|Orientation=plus
|GMAF=0.09917
|Gene_s=AKAP7
|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 | 6.2 | 22.1 | 71.7
| HCB | 0.0 | 2.2 | 97.8
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 2.1 | 97.9
| ASW | 0.0 | 16.1 | 83.9
| CHB | 0.0 | 2.2 | 97.8
| CHD | 0.0 | 0.9 | 99.1
| GIH | 2.0 | 25.7 | 72.3
| LWK | 0.0 | 9.2 | 90.8
| MEX | 0.0 | 17.2 | 82.8
| MKK | 0.0 | 26.5 | 73.5
| TSI | 7.0 | 32.0 | 61.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23502783
  |Trait=Multiple myeloma (IgH translocation)
  |Title=The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
  |RiskAllele=A
  |Pval=6E-6
  |OR=1.60
  |ORtxt=[1.31-1.96]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}