{{Rsnum
|rsid=12190287
|Gene=TCF21
|Chromosome=6
|position=133893387
|Orientation=plus
|GMAF=0.3485
|Gene_s=LOC100288120,TCF21
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 35.4 | 48.7 | 15.9
| HCB | 42.3 | 43.8 | 13.9
| JPT | 34.5 | 46.9 | 18.6
| YRI | 91.2 | 8.8 | 0.0
| ASW | 82.5 | 15.8 | 1.8
| CHB | 42.3 | 43.8 | 13.9
| CHD | 35.8 | 45.9 | 18.3
| GIH | 20.8 | 50.5 | 28.7
| LWK | 98.2 | 1.8 | 0.0
| MEX | 39.7 | 32.8 | 27.6
| MKK | 66.0 | 32.1 | 1.9
| TSI | 39.2 | 44.1 | 16.7
| HapMapRevision=28
}}
{{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
|PMID=20403199
|Title=High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.
|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=G
  |Pval=2E-9
  |OR=1.11
  |ORtxt=[1.08-1.15]
  }}
{{PMID Auto GWAS
|PMID=21378990
|Trait=Coronary artery disease
|Title=Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
|RiskAllele=C
|Pval=1E-12
|OR=1.0800
|ORtxt=[1.06-1.10]
|OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}