{{Rsnum
|rsid=8060686
|Gene=EDC4
|Chromosome=16
|position=67877614
|Orientation=plus
|GMAF=0.2929
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=EDC4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 23.0 | 75.2
| HCB | 1.5 | 10.2 | 88.3
| JPT | 0.9 | 15.0 | 84.1
| YRI | 61.2 | 35.4 | 3.4
| ASW | 45.6 | 36.8 | 17.5
| CHB | 1.5 | 10.2 | 88.3
| CHD | 0.0 | 23.1 | 76.9
| GIH | 4.0 | 32.7 | 63.4
| LWK | 57.3 | 37.3 | 5.5
| MEX | 7.0 | 40.4 | 52.6
| MKK | 47.4 | 44.9 | 7.7
| TSI | 4.9 | 28.4 | 66.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21347282
|Trait=None
|Title=Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
|RiskAllele=T
|Pval=0.000008
|OR=0.0715
|ORtxt=[0.04-0.10] SD decrease
|OA=1
}}

{{PMID Auto GWAS
|PMID=22399527
|Trait=None
|Title=Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.
|RiskAllele=T
|Pval=2E-10
|OR=0.1100
|ORtxt=None
|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}}