{{Rsnum
|rsid=2814944
|Chromosome=6
|position=34585020
|Orientation=plus
|GMAF=0.1382
|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 | 2.7 | 23.2 | 74.1
| HCB | 0.0 | 2.2 | 97.8
| JPT | 0.0 | 0.9 | 99.1
| YRI | 8.4 | 44.8 | 46.9
| ASW | 7.0 | 36.8 | 56.1
| CHB | 0.0 | 2.2 | 97.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 2.0 | 18.8 | 79.2
| LWK | 8.3 | 43.1 | 48.6
| MEX | 1.8 | 20.0 | 78.2
| MKK | 8.6 | 43.7 | 47.7
| TSI | 4.9 | 13.7 | 81.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20686565
|Trait=None
|Title=Biological, clinical and population relevance of 95 loci for blood lipids.
|RiskAllele=A
|Pval=4E-9
|OR=0.4900
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=18535201
|Title=A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}