{{Rsnum
|rsid=12316150
|Gene=OLR1
|Chromosome=12
|position=10159692
|Orientation=plus
|GMAF=0.04821
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=OLR1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 95.2 | 4.8 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| 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
}}[[rs12316150]], a SNP also known as +1071, is located in the 3' untranslated region of the oxidized low density lipoprotein (lectin-like) receptor 1 [[OLR1]] gene, which is also known as the LOX-1 gene.

The [[rs12316150]] risk allele has been associated with increased risk for [[Alzheimer's disease]] in several studies of ~200 Southern Italian Alzheimer patients, but only within the context of a haplotype including one or both of neighboring SNPs [[rs1050283]] and [[rs669]].[PMID 15860461, PMID 18191876]
{{ neighbor
| rsid = 1050283
| distance = 2
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}