{{Rsnum
|rsid=1320900
|Gene=CPNE4
|Chromosome=3
|position=131994722
|Orientation=minus
|GMAF=0.314
|Gene_s=CPNE4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 9.7 | 50.4 | 39.8
| HCB | 10.4 | 51.9 | 37.8
| JPT | 13.6 | 49.1 | 37.3
| YRI | 0.7 | 19.7 | 79.6
| ASW | 0.0 | 22.8 | 77.2
| CHB | 10.4 | 51.9 | 37.8
| CHD | 13.9 | 42.6 | 43.5
| GIH | 15.8 | 45.5 | 38.6
| LWK | 2.8 | 29.6 | 67.6
| MEX | 15.5 | 58.6 | 25.9
| MKK | 8.5 | 49.7 | 41.8
| TSI | 14.9 | 42.6 | 42.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22959728
  |Trait=Amyotrophic lateral sclerosis
  |Title=Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
  |RiskAllele=
  |Pval=7E-6
  |OR=1.19
  |ORtxt=[1.09-1.3]
  |OA=1
}}

{{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}}