{{Rsnum
|rsid=6575353
|Gene=PRIMA1
|Chromosome=14
|position=93738999
|Orientation=plus
|GMAF=0.2502
|Gene_s=PRIMA1
|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 | 82.3 | 17.7 | 0.0
| HCB | 18.2 | 61.3 | 20.4
| JPT | 24.8 | 54.9 | 20.4
| YRI | 55.8 | 38.1 | 6.1
| ASW | 36.8 | 56.1 | 7.0
| CHB | 18.2 | 61.3 | 20.4
| CHD | 22.9 | 48.6 | 28.4
| GIH | 61.4 | 31.7 | 6.9
| LWK | 48.2 | 47.3 | 4.5
| MEX | 65.5 | 32.8 | 1.7
| MKK | 51.3 | 40.4 | 8.3
| TSI | 81.4 | 17.6 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22754043
  |Trait=Insomnia (caffeine-induced)
  |Title=A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.
  |RiskAllele=
  |Pval=1E-6
  |OR=1.47
  |ORtxt=[1.12-1.89]
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}