{{Rsnum
|rsid=11610206
|Chromosome=12
|position=47245743
|Orientation=plus
|GMAF=0.1065
|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 | 1.8 | 19.5 | 78.8
| HCB | 1.5 | 26.3 | 72.3
| JPT | 0.0 | 12.4 | 87.6
| YRI | 0.7 | 21.1 | 78.2
| ASW | 1.8 | 22.8 | 75.4
| CHB | 1.5 | 26.3 | 72.3
| CHD | 2.8 | 26.9 | 70.4
| GIH | 1.0 | 15.8 | 83.2
| LWK | 0.0 | 15.5 | 84.5
| MEX | 0.0 | 10.3 | 89.7
| MKK | 0.0 | 19.4 | 80.6
| TSI | 0.0 | 21.6 | 78.4
| HapMapRevision=28
}}
[http://www.news-medical.net/?id=44594 news] [[Alzheimer's disease]]

{{PMID Auto GWAS
|PMID=19118814
|Trait=Alzheimer's disease
|Title=Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease
|RiskAllele=
|Pval=3E-7
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PharmGKB
|RSID=rs11610206
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19118814; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. (Initial Sample Size: 492 cases, 496 controls; Replication Sample Size: 238 cases, 220 controls); (Region: 12q13.11; Reported Gene(s): FAM113B; Risk Allele: rs11610206-?); (p-value= 0.0000003).This variant is associated with Alzheimer's disease.
|Drugs=
|Drug Classes=
|Diseases=Alzheimer Disease
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740091
}}

{{PMID Auto
|PMID=20883677
|Title=Genetic association of rs11610206 SNP on chromosome 12q13 with late-onset Alzheimer's disease in a Han Chinese population
}}

{{PharmGKB
|RSID=rs11610206
|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=PA162363825
}}

{{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=rs11610206
|overall_frequency_n=16
|overall_frequency_d=128
|overall_frequency=0.125
|n_genomes=9
|n_genomes_annotated=0
|n_haplomes=11
|n_articles=1
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}