{{Rsnum
|rsid=1480090
|Chromosome=15
|position=98172432
|Orientation=minus
|GMAF=0.3994
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 24.8 | 48.7 | 26.5
| HCB | 14.0 | 40.4 | 45.6
| JPT | 7.1 | 32.1 | 60.7
| YRI | 23.3 | 47.9 | 28.8
| ASW | 14.0 | 43.9 | 42.1
| CHB | 14.0 | 40.4 | 45.6
| CHD | 17.4 | 46.8 | 35.8
| GIH | 23.8 | 50.5 | 25.7
| LWK | 12.8 | 40.4 | 46.8
| MEX | 13.8 | 39.7 | 46.6
| MKK | 12.3 | 51.6 | 36.1
| TSI | 18.6 | 50.0 | 31.4
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs1480090
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19118814
|Annotation=This variant is significantly associated with late-onset Alzheimer disease (LOAD) in a GWAS study with 492 LOAD cases and 498 cognitive controls using Illumina's HumanHap550 beadchip.
|Drugs=
|Drug Classes=
|Diseases=Alzheimer Disease
|Curation Level=Curated
|PharmGKB Accession ID=PA162363831
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1480090
|overall_frequency_n=74
|overall_frequency_d=128
|overall_frequency=0.578125
|n_genomes=47
|n_genomes_annotated=0
|n_haplomes=68
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{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}}