{{Rsnum
|rsid=1336472
|Gene=AK4
|Chromosome=1
|position=65230247
|Orientation=minus
|GMAF=0.3797
|Gene_s=AK4
|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 | 39.8 | 43.4 | 16.8
| HCB | 8.0 | 41.6 | 50.4
| JPT | 6.2 | 46.0 | 47.8
| YRI | 0.0 | 1.4 | 98.6
| ASW | 0.0 | 33.3 | 66.7
| CHB | 8.0 | 41.6 | 50.4
| CHD | 11.9 | 37.6 | 50.5
| GIH | 25.7 | 53.5 | 20.8
| LWK | 0.0 | 2.7 | 97.3
| MEX | 27.6 | 31.0 | 41.4
| MKK | 0.6 | 16.0 | 83.3
| TSI | 44.1 | 43.1 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=G
  |Pval=4E-10
  |OR=1.54
  |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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}