{{Rsnum
|rsid=7613868
|Chromosome=3
|position=124023182
|Orientation=plus
|GMAF=0.4949
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 54.0 | 43.4 | 2.7
| HCB | 29.9 | 48.2 | 21.9
| JPT | 35.4 | 46.0 | 18.6
| YRI | 0.7 | 19.7 | 79.6
| ASW | 3.5 | 26.3 | 70.2
| CHB | 29.9 | 48.2 | 21.9
| CHD | 32.1 | 43.1 | 24.8
| GIH | 45.5 | 41.6 | 12.9
| LWK | 0.9 | 13.6 | 85.5
| MEX | 46.6 | 43.1 | 10.3
| MKK | 4.5 | 39.1 | 56.4
| TSI | 44.1 | 44.1 | 11.8
| HapMapRevision=28
}}{{Report GE
|PubMed=17357071
|Source=OMIM
|AffyProbeset=SNP_A-8580439
|AffyOrientation=same
|AlleleA=C
|AlleleB=T
|onGW5=0
|rsid=7613868
|ancestral=T
|RiskPopulation=Caucasian
|RiskAllele=T
|CaseFreq=0.37
|ControlFreq=0.26
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.80
|Disease=Coronary artery disease
|DiseaseSymbol=CAD
|OA=1
}}

rs7613868 increases susceptibility to Atherosclerosis 2.60 times for carriers of the T allele {{PMID|17357071|OA=1
}}

rs7613868 increases susceptibility to Coronary artery disease 1.80 times for carriers of the T allele {{PMID|17357071|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}