{{Rsnum
|rsid=974819
|Chromosome=11
|position=103789839
|Orientation=minus
|GMAF=0.4183
|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 | 7.3 | 29.4 | 63.3
| HCB | 36.3 | 49.6 | 14.1
| JPT | 31.5 | 54.1 | 14.4
| YRI | 28.3 | 53.8 | 17.9
| ASW | 24.6 | 56.1 | 19.3
| CHB | 36.3 | 49.6 | 14.1
| CHD | 38.3 | 53.3 | 8.4
| GIH | 11.0 | 41.0 | 48.0
| LWK | 40.4 | 48.6 | 11.0
| MEX | 6.9 | 37.9 | 55.2
| MKK | 21.9 | 52.3 | 25.8
| TSI | 11.0 | 47.0 | 42.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21378988
|Trait=Coronary heart disease
|Title=A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
|RiskAllele=T
|Pval=2E-9
|OR=1.0700
|ORtxt=[1.04-1.09]
}}

{{PMID Auto
|PMID=22704460
|Title=A case-control study provides evidence of association for a common SNP rs974819 in PDGFD to coronary heart disease and suggests a sex-dependent effect
}}

{{PMID Auto
|PMID=23364394
|Title=A genome-wide association study of a coronary artery disease risk variant
}}

{{PMID Auto
|PMID=24573017
|Title=Associations between the CDKN2A/B, ADTRP and PDGFD Polymorphisms and the Development of Coronary Atherosclerosis in Japanese Patients
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}