{{Rsnum
|rsid=13213247
|Chromosome=6
|position=80806319
|Orientation=plus
|GMAF=0.09229
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 89.2 | 9.9 | 0.9
| HCB | 70.1 | 25.5 | 4.4
| JPT | 65.5 | 33.6 | 0.9
| YRI | 80.8 | 18.5 | 0.7
| ASW | 82.5 | 17.5 | 0.0
| CHB | 70.1 | 25.5 | 4.4
| CHD | 61.3 | 33.0 | 5.7
| GIH | 72.4 | 27.6 | 0.0
| LWK | 81.7 | 18.3 | 0.0
| MEX | 87.5 | 12.5 | 0.0
| MKK | 88.1 | 11.9 | 0.0
| TSI | 86.3 | 13.7 | 0.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs13213247
|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=PA162363843
}}

{{PMID|19756043|OA=1
}} A simple and efficient algorithm for genome-wide homozygosity analysis in disease.

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs13213247
|overall_frequency_n=5
|overall_frequency_d=122
|overall_frequency=0.0409836
|n_genomes=4
|n_genomes_annotated=0
|n_haplomes=4
|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}}