{{Rsnum
|rsid=2298814
|Gene=SORL1
|Chromosome=11
|position=121554173
|Orientation=minus
|GMAF=0.04775
|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 | 95.6 | 4.4 | 0.0
| HCB | 90.5 | 9.5 | 0.0
| JPT | 74.3 | 24.8 | 0.9
| YRI | 90.5 | 9.5 | 0.0
| ASW | 82.5 | 15.8 | 1.8
| CHB | 90.5 | 9.5 | 0.0
| CHD | 86.2 | 12.8 | 0.9
| GIH | 95.0 | 5.0 | 0.0
| LWK | 80.0 | 20.0 | 0.0
| MEX | 93.1 | 6.9 | 0.0
| MKK | 86.5 | 12.8 | 0.6
| TSI | 97.1 | 2.0 | 1.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs2298814
|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=PA162363859
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2298814
|overall_frequency_n=9
|overall_frequency_d=128
|overall_frequency=0.0703125
|n_genomes=9
|n_genomes_annotated=0
|n_haplomes=9
|n_articles=0
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=2
|webscore=N
|n_web_uneval=6
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}