{{Rsnum
|rsid=2072183
|Gene=NPC1L1
|Chromosome=7
|position=44539581
|Orientation=minus
|GMAF=0.2723
|Gene_s=NPC1L1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 52.3 | 43.1 | 4.6
| HCB | 46.7 | 35.6 | 17.8
| JPT | 37.8 | 53.3 | 8.9
| YRI | 61.9 | 34.9 | 3.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 46.7 | 35.6 | 17.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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-11
|OR=1.1700
|ORtxt=None
|OA=1
}}
{{PMID Auto
|PMID=22646906
|Title=Association of rs2072183 SNP and serum lipid levels in the Mulao and Han populations
|OA=1
}}

{{PMID Auto
|PMID=23482652
|Title=Novel gene-by-environment interactions: APOB and NPC1L1 variants affect the relationship between dietary and total plasma cholesterol
|OA=1
}}

{{PMID Auto
|PMID=24861377
|Title=Gene polymorphism and frequencies of the NPC1L1 Gene (rs2072183, rs217434 and rs217428) in Japanese patients with dyslipidemia
}}
{{on chip | HumanOmni1Quad}}