{{Rsnum
|rsid=4773144
|Gene=COL4A2
|Chromosome=13
|position=110308365
|Orientation=plus
|GMAF=0.4073
|Gene_s=COL4A1,COL4A2
|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 | 33.6 | 48.7 | 17.7
| HCB | 24.8 | 57.7 | 17.5
| JPT | 42.9 | 44.6 | 12.5
| YRI | 50.3 | 38.6 | 11.0
| ASW | 54.4 | 36.8 | 8.8
| CHB | 24.8 | 57.7 | 17.5
| CHD | 35.8 | 52.3 | 11.9
| GIH | 25.7 | 56.4 | 17.8
| LWK | 30.9 | 50.0 | 19.1
| MEX | 20.7 | 63.8 | 15.5
| MKK | 20.1 | 48.1 | 31.8
| TSI | 24.0 | 49.0 | 27.0
| HapMapRevision=28
}}

[[Coronary Heart Disease]]

{{PMID Auto
|PMID=4021556
|Title=Analysis of common and coding variants with cardiovascular disease in the diabetes heart study.
}}
{{PMID Auto |PMID=3584137
|Title=Improvement in Prediction of Coronary Heart Disease Risk over Conventional Risk Factors Using SNPs Identified in Genome-Wide Association Studies.
}}
{{PMID Auto
|PMID=3583714
|Title=Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study
}}
{{PMID Auto|PMID=3266236
|Title=Genetic Profiling Using Genome-Wide Significant Coronary Artery Disease Risk Variants Does Not Improve the Prediction of Subclinical Atherosclerosis: The Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey – A Meta-Analysis of Three Independent Studies
|OA=1
}}
{{PMID Auto
|PMID=3179381
|Title=Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.
}}
{{PMID Auto|PMID=3178591
|Title=Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease.
}}
{{PMID Auto
|PMID=24573017
|Title=Associations between the CDKN2A/B, ADTRP and PDGFD Polymorphisms and the Development of Coronary Atherosclerosis in Japanese Patients.
}}
{{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=G
  |Pval=2E-6
  |OR=1.08
  |ORtxt=[1.05-1.12]
  }}
{{PMID Auto GWAS
|PMID=21378990
|Trait=Coronary heart disease
|Title=Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
|RiskAllele=G
|Pval=4E-9
|OR=1.0700
|ORtxt=[1.05-1.09]
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}