{{Rsnum
|rsid=6065904
|Gene=PLTP
|Chromosome=20
|position=45906012
|Orientation=plus
|GMAF=0.27
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PLTP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 5.3 | 31.9 | 62.8
| HCB | 7.3 | 41.6 | 51.1
| JPT | 15.0 | 47.8 | 37.2
| YRI | 4.1 | 30.6 | 65.3
| ASW | 1.8 | 28.1 | 70.2
| CHB | 7.3 | 41.6 | 51.1
| CHD | 8.3 | 43.5 | 48.1
| GIH | 15.8 | 41.6 | 42.6
| LWK | 5.5 | 29.4 | 65.1
| MEX | 22.4 | 50.0 | 27.6
| MKK | 8.3 | 42.3 | 49.4
| TSI | 2.9 | 31.4 | 65.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=19965587
|Title=Genetic and nongenetic sources of variation in phospholipid transfer protein activity
|OA=1
}}

{{PMID Auto GWAS
|PMID=22286219
|Trait=None
|Title=Genome-wide association study identifies multiple loci influencing human serum metabolite levels.
|RiskAllele=
|Pval=2E-31
|OR=0.2200
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=21347282
|Title=Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}