{{Rsnum
|rsid=1425967
|Chromosome=4
|position=137367736
|Orientation=minus
|GMAF=0.4564
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 17.9 | 51.8 | 30.4
| HCB | 27.0 | 46.7 | 26.3
| JPT | 23.0 | 54.0 | 23.0
| YRI | 52.4 | 44.2 | 3.4
| ASW | 56.1 | 38.6 | 5.3
| CHB | 27.0 | 46.7 | 26.3
| CHD | 20.2 | 53.2 | 26.6
| GIH | 2.0 | 49.0 | 49.0
| LWK | 45.5 | 44.5 | 10.0
| MEX | 43.9 | 43.9 | 12.3
| MKK | 41.7 | 50.6 | 7.7
| TSI | 16.7 | 52.0 | 31.4
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs1425967
|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=PA162363841
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1425967
|overall_frequency_n=74
|overall_frequency_d=128
|overall_frequency=0.578125
|n_genomes=47
|n_genomes_annotated=0
|n_haplomes=67
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}