{{Rsnum
|rsid=11159647
|Chromosome=14
|position=84308865
|Orientation=plus
|GMAF=0.2759
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 31.5 | 33.3 | 35.1
| HCB | 5.8 | 39.4 | 54.7
| JPT | 3.5 | 39.8 | 56.6
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 17.5 | 82.5
| CHB | 5.8 | 39.4 | 54.7
| CHD | 5.5 | 32.1 | 62.4
| GIH | 17.8 | 47.5 | 34.7
| LWK | 0.0 | 2.7 | 97.3
| MEX | 6.9 | 50.0 | 43.1
| MKK | 1.3 | 24.4 | 74.4
| TSI | 19.6 | 46.1 | 34.3
| HapMapRevision=28
}}[http://www.genomeweb.com/issues/news/150344-1.html genomeweb] [[rs4420638]] [[rs11159647]] and [[rs3826656]] were also significantly associated with [[Alzheimer's disease]]

{{PMID Auto GWAS
|PMID=18976728
|Trait=Alzheimer's disease
|Title=Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE
|RiskAllele=
|Pval=0.000002
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PharmGKB
|RSID=rs11159647
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:18976728; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE. (Initial Sample Size: 941 affected individuals, 404 unaffected individuals; Replication Sample Size: 1,767 affected individuals, 838 unaffected individuals); (Region: 14q31.2; Reported Gene(s): Intergenic; Risk Allele: rs11159647-?); (p-value= 0.000002).This variant is associated with Alzheimer's disease.
|Drugs=
|Drug Classes=
|Diseases=Alzheimer Disease
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740768
}}

{{PharmGKB
|RSID=rs11159647
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:18976728
|Annotation=In a GWAS of Alzheimer Disease families of self-reported European ancestry, this SNP was found to be associated with Alzheimer Disease. This association was replicated in three other family samples and in an independent set of case-controls.
|Drugs=
|Drug Classes=
|Diseases=Alzheimer Disease
|Curation Level=Curated
|PharmGKB Accession ID=PA162356252
}}

{{PMID Auto
|PMID=19640594
|Title=Recent insights into the molecular genetics of dementia.
|OA=1
}}

{{PMID Auto
|PMID=20061627
|Title=Genome-wide scan of copy number variation in late-onset Alzheimer's disease.
|OA=1
}}

{{PMID Auto
|PMID=20574532
|Title=Intermediate phenotypes identify divergent pathways to Alzheimer's disease.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11159647
|overall_frequency_n=35
|overall_frequency_d=128
|overall_frequency=0.273438
|n_genomes=24
|n_genomes_annotated=0
|n_haplomes=31
|n_articles=1
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}