{{Rsnum
|rsid=4773460
|Chromosome=13
|position=86590602
|Orientation=plus
|GMAF=0.2167
|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 | 80.0 | 18.5 | 1.5
| HCB | 73.3 | 26.7 | 0.0
| JPT | 58.3 | 38.9 | 2.8
| YRI | 26.8 | 51.4 | 21.8
| ASW | 35.1 | 56.1 | 8.8
| CHB | 73.3 | 26.7 | 0.0
| CHD | 79.0 | 19.0 | 1.9
| GIH | 81.0 | 17.0 | 2.0
| LWK | 22.2 | 50.0 | 27.8
| MEX | 64.9 | 31.6 | 3.5
| MKK | 38.5 | 48.7 | 12.8
| TSI | 73.3 | 25.7 | 1.0
| 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=0.000002
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4773460
|overall_frequency_n=26
|overall_frequency_d=128
|overall_frequency=0.203125
|n_genomes=20
|n_genomes_annotated=0
|n_haplomes=22
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}