{{Rsnum
|rsid=715948
|Gene=LRP1
|Chromosome=12
|position=57139199
|Orientation=minus
|GMAF=0.3384
|Gene_s=LRP1
|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 | 9.7 | 49.6 | 40.7
| HCB | 25.5 | 45.3 | 29.2
| JPT | 39.8 | 45.1 | 15.0
| YRI | 3.4 | 28.6 | 68.0
| ASW | 3.5 | 21.1 | 75.4
| CHB | 25.5 | 45.3 | 29.2
| CHD | 26.6 | 50.5 | 22.9
| GIH | 10.9 | 33.7 | 55.4
| LWK | 6.4 | 36.4 | 57.3
| MEX | 15.5 | 43.1 | 41.4
| MKK | 7.1 | 46.2 | 46.8
| TSI | 6.9 | 40.2 | 52.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=22347399
|Title=Preliminary Evidence for an Association between LRP-1 Genotype and Body Mass Index in Humans
|OA=1
}}

{{PMID Auto
|PMID=19503741
|Title=Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
|OA=1
}}

{{PMID Auto
|PMID=19753309
|Title=SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
|OA=1
}}

{{PMID Auto
|PMID=20157514
|Title=Positive association of common variants in CD36 with neovascular age-related macular degeneration.
|OA=1
}}

{{PMID Auto
|PMID=21741043
|Title=Genetic variability within the cholesterol lowering pathway and the effectiveness of statins in reducing the risk of MI.
|OA=1
}}

{{PMID Auto
|PMID=22819221
|Title=LRP1 gene polymorphisms are associated with premature risk of cardiovascular disease in patients with familial hypercholesterolemia.
}}

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