{{Rsnum
|rsid=2972146
|Chromosome=2
|position=226235982
|Orientation=minus
|GMAF=0.2259
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 41.9 | 33.9 | 24.2
| HCB | 84.1 | 15.9 | 0.0
| JPT | 88.6 | 11.4 | 0.0
| YRI | 83.3 | 16.7 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 84.1 | 15.9 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20686565
|Trait=None
|Title=Biological, clinical and population relevance of 95 loci for blood lipids.
|RiskAllele=C
|Pval=2E-9
|OR=0.4600
|ORtxt=None
|OA=1
}}
{{PMID Auto
|PMID=23659870
|Title=Common variants in and near IRS1 and subclinical cardiovascular disease in the Framingham Heart Study
}}