{{Rsnum
|rsid=4845552
|Chromosome=1
|position=153507522
|Orientation=plus
|GMAF=0.1272
|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 | 68.1 | 26.5 | 5.3
| HCB | 74.5 | 23.4 | 2.2
| JPT | 81.4 | 17.7 | 0.9
| YRI | 74.1 | 25.9 | 0.0
| ASW | 63.2 | 31.6 | 5.3
| CHB | 74.5 | 23.4 | 2.2
| CHD | 84.4 | 15.6 | 0.0
| GIH | 84.2 | 15.8 | 0.0
| LWK | 76.4 | 22.7 | 0.9
| MEX | 84.5 | 15.5 | 0.0
| MKK | 73.1 | 25.0 | 1.9
| TSI | 72.5 | 25.5 | 2.0
| 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=0.000006
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4845552
|overall_frequency_n=115
|overall_frequency_d=128
|overall_frequency=0.898438
|n_genomes=55
|n_genomes_annotated=0
|n_haplomes=101
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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