{{Rsnum
|rsid=12146962
|Chromosome=14
|position=32911892
|Orientation=plus
|GMAF=0.4252
|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 | 9.1 | 52.7 | 38.2
| HCB | 14.7 | 54.4 | 30.9
| JPT | 14.5 | 45.5 | 40.0
| YRI | 4.8 | 47.6 | 47.6
| ASW | 7.0 | 49.1 | 43.9
| CHB | 14.7 | 54.4 | 30.9
| CHD | 15.1 | 58.5 | 26.4
| GIH | 17.8 | 45.5 | 36.6
| LWK | 19.1 | 46.4 | 34.5
| MEX | 10.3 | 34.5 | 55.2
| MKK | 32.5 | 52.3 | 15.2
| TSI | 31.0 | 48.0 | 21.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs12146962
|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=PA162363829
}}

{{PMID Auto GWAS
|PMID=22138694
|Trait=None
|Title=A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis.
|RiskAllele=
|Pval=0.000009
|OR=1.1400
|ORtxt=None
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12146962
|overall_frequency_n=55
|overall_frequency_d=128
|overall_frequency=0.429688
|n_genomes=38
|n_genomes_annotated=0
|n_haplomes=47
|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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}