{{Rsnum
|rsid=10105606
|Chromosome=8
|position=19970337
|Orientation=plus
|GMAF=0.3788
|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 | 11.5 | 38.9 | 49.6
| HCB | 2.9 | 30.7 | 66.4
| JPT | 6.2 | 27.7 | 66.1
| YRI | 58.3 | 34.0 | 7.6
| ASW | 25.0 | 64.3 | 10.7
| CHB | 2.9 | 30.7 | 66.4
| CHD | 5.5 | 33.0 | 61.5
| GIH | 3.0 | 38.0 | 59.0
| LWK | 55.0 | 37.6 | 7.3
| MEX | 16.1 | 33.9 | 50.0
| MKK | 40.4 | 50.0 | 9.6
| TSI | 18.8 | 36.6 | 44.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20864672
|Trait=None
|Title=Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
|RiskAllele=C
|Pval=4E-26
|OR=0.07
|ORtxt=[0.06-0.08] increase
|OA=1
}}

{{PMID Auto
|PMID=19041386
|Title=Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.
|OA=1
}}

{{PMID Auto
|PMID=19148283
|Title=Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study.
|OA=1
}}

{{PMID Auto
|PMID=23832694
|Title=Common genetic variants associated with lipid profiles in a Chinese pediatric population.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}