{{Rsnum
|rsid=1699102
|Gene=SORL1
|Chromosome=11
|position=121586253
|Orientation=plus
|GMAF=0.4541
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SORL1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 10.7 | 40.2 | 49.1
| HCB | 82.1 | 17.2 | 0.7
| JPT | 54.0 | 40.7 | 5.3
| YRI | 25.2 | 53.1 | 21.8
| ASW | 26.3 | 59.6 | 14.0
| CHB | 82.1 | 17.2 | 0.7
| CHD | 81.3 | 17.8 | 0.9
| GIH | 51.0 | 41.0 | 8.0
| LWK | 31.2 | 45.0 | 23.9
| MEX | 31.0 | 41.4 | 27.6
| MKK | 16.7 | 57.1 | 26.3
| TSI | 8.8 | 43.1 | 48.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=18063222
|Title=SORL1 haplotypes modulate risk of Alzheimer's disease in Chinese
}}

{{PMID Auto
|PMID=19584446
|Title=A study of the SORL1 gene in Alzheimer's disease and cognitive function
}}

{{PMID Auto
|PMID=17826910
|Title=Association between genetic variants in sortilin-related receptor 1 (SORL1) and Alzheimer's disease in adults with Down syndrome.
|OA=1
}}

{{PMID Auto
|PMID=18938222
|Title=Allelic mRNA expression of sortilin-1 (SORL1) mRNA in Alzheimer's autopsy brain tissues.
|OA=1
}}

{{PMID Auto
|PMID=19064752
|Title=Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease.
|OA=1
}}

{{PMID Auto
|PMID=20667857
|Title=Genetic risk factors for cerebral small-vessel disease in hypertensive patients from a genetically isolated population.
}}

{{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}}