{{Rsnum
|rsid=3843763
|Gene=PLTP
|Chromosome=20
|position=45919554
|Orientation=plus
|GMAF=0.3182
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Summary=lower HDL cholesterol
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}The (T) allele of [[rs3843763]] was associated with risk for lower high-density lipoprotein (HDL) [[cholesterol]] plasma levels in 3 independent population samples, including both Caucasians and African-Americans.{{PMID|17952847|OA=1
}}

{{omim
|id=172425
|desc=PHOSPHOLIPID TRANSFER PROTEIN; PLTP
|rsnum=3843763
}}

{{PharmGKB
|RSID=rs3843763
|Name_s=
|Gene_s=PLTP
|Feature=
|Evidence=PubMed ID:17952847
|Annotation=This SNP has been associated with small changes in HDL cholesterol levels. The T allele has been correlated with lower HDL.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Curated
|PharmGKB Accession ID=PA161613797
}}

{{omim
|id=172425
|rsnum=3843763
|variant=0001
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3843763
|overall_frequency_n=41
|overall_frequency_d=128
|overall_frequency=0.320312
|n_genomes=28
|n_genomes_annotated=0
|n_haplomes=35
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}