{{Rsnum
|rsid=7841189
|Chromosome=8
|position=19987865
|Orientation=plus
|GMAF=0.1488
|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 | 76.1 | 20.4 | 3.5
| HCB | 81.8 | 17.5 | 0.7
| JPT | 81.4 | 17.7 | 0.9
| YRI | 58.5 | 36.1 | 5.4
| ASW | 56.1 | 42.1 | 1.8
| CHB | 81.8 | 17.5 | 0.7
| CHD | 77.1 | 22.0 | 0.9
| GIH | 79.2 | 20.8 | 0.0
| LWK | 68.2 | 26.4 | 5.5
| MEX | 81.0 | 19.0 | 0.0
| MKK | 76.3 | 22.4 | 1.3
| TSI | 63.7 | 31.4 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22399527
|Trait=None
|Title=Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.
|RiskAllele=C
|Pval=1E-14
|OR=0.1800
|ORtxt=None
|OA=1
}}

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