{{Rsnum
|rsid=11626056
|Chromosome=14
|position=51766558
|Orientation=plus
|GMAF=0.3292
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RP11-280K24.4
|Gene_s=RP11-280K24.4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 46.8 | 34.2 | 18.9
| HCB | 27.4 | 49.6 | 23.0
| JPT | 21.6 | 53.2 | 25.2
| YRI | 88.4 | 11.6 | 0.0
| ASW | 84.2 | 14.0 | 1.8
| CHB | 27.4 | 49.6 | 23.0
| CHD | 37.6 | 44.0 | 18.3
| GIH | 47.5 | 37.6 | 14.9
| LWK | 81.8 | 18.2 | 0.0
| MEX | 29.8 | 52.6 | 17.5
| MKK | 53.9 | 39.6 | 6.5
| TSI | 30.0 | 53.0 | 17.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19668339
|Trait=Hippocampal atrophy
|Title=Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
|RiskAllele=
|Pval=0.000001
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11626056
|overall_frequency_n=21
|overall_frequency_d=104
|overall_frequency=0.201923
|n_genomes=13
|n_genomes_annotated=0
|n_haplomes=17
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}