{{Rsnum
|rsid=1010159
|Gene=SORL1
|Chromosome=11
|position=121612692
|Orientation=minus
|GMAF=0.4876
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SORL1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 44.6 | 42.9 | 12.5
| HCB | 21.2 | 43.1 | 35.8
| JPT | 24.8 | 54.0 | 21.2
| YRI | 13.6 | 46.3 | 40.1
| ASW | 22.8 | 56.1 | 21.1
| CHB | 21.2 | 43.1 | 35.8
| CHD | 17.4 | 49.5 | 33.0
| GIH | 10.9 | 50.5 | 38.6
| LWK | 15.5 | 43.6 | 40.9
| MEX | 22.4 | 46.6 | 31.0
| MKK | 12.2 | 52.6 | 35.3
| TSI | 47.1 | 44.1 | 8.8
| HapMapRevision=28
}}{{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=17903297
|Title=Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.
|OA=1
}}

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

{{PMID Auto
|PMID=18813964
|Title=Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid beta.
|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=19362127
|Title=Endophenotypes in normal brain morphology and Alzheimer's disease: a review.
|OA=1
}}

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

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

{{PMID Auto
|PMID=20061642
|Title=Use of genetic variation as biomarkers for mild cognitive impairment and progression of mild cognitive impairment to dementia.
|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 | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}