{{Rsnum
|rsid=383830
|Chromosome=5
|position=100613278
|Orientation=minus
|GMAF=0.208
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 61.9 | 34.5 | 3.5
| HCB | 65.7 | 30.7 | 3.6
| JPT | 66.4 | 29.2 | 4.4
| YRI | 34.0 | 46.9 | 19.0
| ASW | 36.8 | 52.6 | 10.5
| CHB | 65.7 | 30.7 | 3.6
| CHD | 65.1 | 31.2 | 3.7
| GIH | 77.2 | 20.8 | 2.0
| LWK | 48.2 | 36.4 | 15.5
| MEX | 72.4 | 25.9 | 1.7
| MKK | 44.2 | 44.2 | 11.5
| TSI | 65.7 | 31.4 | 2.9
| HapMapRevision=28
}}
[[rs383830]] has been reported in a large study to be associated with [[heart disease]], in particular, [[coronary artery disease]].

The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with heterozygotes is 1.60 (CI 1.16-2.21), and for homozygotes, 1.92 (CI 1.40-2.63). {{PMID|17554300|OA=1
}}

{{PMID Auto
|PMID=19956433
|Title=Genetics of coronary artery disease: focus on genome-wide association studies.
|OA=1
}}

{{PMID Auto
|PMID=21804106
|Title=Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}