{{Rsnum
|rsid=2545801
|Chromosome=5
|position=177414338
|Orientation=minus
|GMAF=0.483
|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 | 7.1 | 23.0 | 69.9
| HCB | 44.5 | 47.4 | 8.0
| JPT | 43.4 | 47.8 | 8.8
| YRI | 89.8 | 10.2 | 0.0
| ASW | 59.6 | 31.6 | 8.8
| CHB | 44.5 | 47.4 | 8.0
| CHD | 52.3 | 42.2 | 5.5
| GIH | 32.7 | 51.5 | 15.8
| LWK | 84.5 | 14.5 | 0.9
| MEX | 19.0 | 51.7 | 29.3
| MKK | 60.9 | 34.0 | 5.1
| TSI | 0.0 | 34.3 | 65.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22286219
|Trait=None
|Title=Genome-wide association study identifies multiple loci influencing human serum metabolite levels.
|RiskAllele=
|Pval=9E-11
|OR=0.1200
|ORtxt=None
|OA=1
}}

{{PMID Auto GWAS
|PMID=22703881
|Trait=None
|Title=Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease.
|RiskAllele=C
|Pval=6E-88
|OR=1.6800
|ORtxt=None
|OA=1
}}

{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}