{{Rsnum
|rsid=12721054
|Gene=APOC1
|Chromosome=19
|position=44919330
|Orientation=plus
|GMAF=0.03122
|Gene_s=APOC1
|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 | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 81.0 | 19.0 | 0.0
| ASW | 66.7 | 31.6 | 1.8
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 70.9 | 28.2 | 0.9
| MEX | 96.6 | 3.4 | 0.0
| MKK | 83.3 | 16.7 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23726366
  |Trait=Triglycerides
  |Title=Genome-wide Characterization of Shared and Distinct Genetic Components that Influence Blood Lipid Levels in Ethnically Diverse Human Populations.
  |RiskAllele=G
  |Pval=3E-19
  |OR=.10
  |ORtxt=[NR] unit decrease
  |OA=1
}}

{{PMID Auto
|PMID=19668339
|Title=Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}