{{Rsnum
|rsid=11848070
|Gene=PCNX
|Chromosome=14
|position=71040884
|Orientation=plus
|GMAF=0.123
|Gene_s=PCNX
|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 | 53.6 | 39.3 | 7.1
| HCB | 94.1 | 5.9 | 0.0
| JPT | 93.8 | 6.2 | 0.0
| YRI | 89.7 | 10.3 | 0.0
| ASW | 86.0 | 14.0 | 0.0
| CHB | 94.1 | 5.9 | 0.0
| CHD | 94.5 | 5.5 | 0.0
| GIH | 83.0 | 17.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 84.5 | 13.8 | 1.7
| MKK | 98.7 | 1.3 | 0.0
| TSI | 61.8 | 34.3 | 3.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22881374
  |Trait=Alzheimer's disease (late onset)
  |Title=Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.
  |RiskAllele=C
  |Pval=6E-6
  |OR=NR
  |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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}