{{Rsnum
|rsid=4953023
|Gene=ABCG8
|Chromosome=2
|position=43846861
|Orientation=plus
|GMAF=0.073
|Gene_s=ABCG8
|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 | 0.9 | 13.4 | 85.7
| HCB | 0.0 | 2.9 | 97.1
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.7 | 13.6 | 85.7
| ASW | 1.8 | 14.3 | 83.9
| CHB | 0.0 | 2.9 | 97.1
| CHD | 0.0 | 4.6 | 95.4
| GIH | 0.0 | 5.0 | 95.0
| LWK | 0.0 | 22.7 | 77.3
| MEX | 0.0 | 27.6 | 72.4
| MKK | 0.0 | 17.9 | 82.1
| TSI | 1.0 | 10.8 | 88.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=22655090
|Title=ATP-Binding Cassette Transporter G5 and G8 Polymorphisms and Several Environmental Factors with Serum Lipid Levels
|OA=1
}}

{{PMID Auto
|PMID=19060906
|Title=Common variants at 30 loci contribute to polygenic dyslipidemia.
|OA=1
}}

{{PMID Auto
|PMID=20502693
|Title=Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.
|OA=1
}}

{{PMID Auto
|PMID=23707316
|Title=High intestinal cholesterol absorption is associated with cardiovascular disease and risk alleles in ABCG8 and ABO: evidence from the LURIC and YFS cohorts and from a meta-analysis
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}