{{Rsnum
|rsid=3824968
|Gene=SORL1
|Chromosome=11
|position=121605213
|Orientation=plus
|ReferenceAllele=T
|GMAF=0.3733
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=SORL1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 12.5 | 37.5 | 50.0
| HCB | 40.0 | 31.1 | 28.9
| JPT | 22.7 | 47.7 | 29.5
| YRI | 3.2 | 20.6 | 76.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 40.0 | 31.1 | 28.9
| 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|18063222}}  [[Alzheimer's disease]] [[rs3824968]]

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

{{PMID Auto
|PMID=21997402
|Title=Impact of SORL1 single nucleotide polymorphisms on Alzheimer's disease cerebrospinal fluid markers
|OA=1
}}

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

{{PMID|18562096|OA=1
}} No association of SORL1 SNPs with Alzheimer's disease.

{{PMID|18713574|OA=1
}} The neuronal sortilin-related receptor gene SORL1 and late-onset Alzheimer's disease.

{{PMID|18830724|OA=1
}} Assessment of Alzheimer's disease case-control associations using family-based methods.

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

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

{{PMID|19362127|OA=1
}} Endophenotypes in normal brain morphology and Alzheimer's disease: a review.

{{PMID|19368828}} Association of SORL1 gene variants with Alzheimer's disease.

{{PMID|19906263|OA=1
}} Use of genetic variation as biomarkers for Alzheimer's disease.

{{PMID|20061642|OA=1
}} Use of genetic variation as biomarkers for mild cognitive impairment and progression of mild cognitive impairment to dementia.

{{PMID|20574532|OA=1
}} Intermediate phenotypes identify divergent pathways to Alzheimer's disease.

{{PMID|20625269}} Amyloid-beta-Related Genes SORL1 and ACE are Genetically Associated With Risk for Late-onset Alzheimer Disease in the Chinese Population.

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

{{PMID Auto
|PMID=24083537
|Title=SORL1 genetic variants modulate risk of amnestic mild cognitive impairment in northern Han Chinese
}}

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