{{Rsnum
|rsid=1878406
|Chromosome=4
|position=147472512
|Orientation=plus
|GMAF=0.1823
|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 | 73.5 | 25.7 | 0.9
| HCB | 65.7 | 27.0 | 7.3
| JPT | 49.6 | 39.8 | 10.6
| YRI | 68.0 | 30.6 | 1.4
| ASW | 59.6 | 35.1 | 5.3
| CHB | 65.7 | 27.0 | 7.3
| CHD | 58.3 | 38.0 | 3.7
| GIH | 65.3 | 31.7 | 3.0
| LWK | 61.8 | 32.7 | 5.5
| MEX | 65.5 | 29.3 | 5.2
| MKK | 63.9 | 32.9 | 3.2
| TSI | 66.3 | 28.7 | 5.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21909108
|Trait=None
|Title=Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.
|RiskAllele=T
|Pval=7E-12
|OR=0.1993
|ORtxt=[0.14-0.26] unit increase
|OA=1
}}

{{PMID Auto GWAS
  |PMID=24262325
  |Trait=Coronary artery disease
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=T
  |Pval=1E-6
  |OR=1.10
  |ORtxt=[1.06-1.14]
  }}
{{on chip | Illumina Human 1M}}