{{Rsnum
|rsid=1792124
|Gene=SORL1
|Chromosome=11
|position=121570811
|Orientation=plus
|GMAF=0.06061
|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 | 0.0 | 4.4 | 95.6
| HCB | 0.0 | 6.6 | 93.4
| JPT | 1.8 | 29.2 | 69.0
| YRI | 4.1 | 17.0 | 78.9
| ASW | 1.8 | 26.3 | 71.9
| CHB | 0.0 | 6.6 | 93.4
| CHD | 0.9 | 9.2 | 89.9
| GIH | 0.0 | 5.0 | 95.0
| LWK | 1.8 | 24.5 | 73.6
| MEX | 0.0 | 6.9 | 93.1
| MKK | 0.6 | 20.5 | 78.8
| TSI | 1.0 | 2.9 | 96.1
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs1792124
|Name_s=
|Gene_s=SORL1
|Feature=
|Evidence=PubMed ID:17553421; PubMed ID:19118814
|Annotation=This variant is nominally associated with late-onset Alzheimer disease (LOAD) in 2 GWAS studies.
|Drugs=
|Drug Classes=
|Diseases=Alzheimer Disease
|Curation Level=Curated
|PharmGKB Accession ID=PA162363858
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1792124
|overall_frequency_n=112
|overall_frequency_d=128
|overall_frequency=0.875
|n_genomes=54
|n_genomes_annotated=0
|n_haplomes=96
|n_articles=0
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}