{{Rsnum
|rsid=7727656
|Chromosome=5
|position=25760570
|Orientation=plus
|GMAF=0.4206
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 5.3 | 38.9 | 55.8
| HCB | 26.5 | 50.7 | 22.8
| JPT | 20.5 | 50.0 | 29.5
| YRI | 42.2 | 49.0 | 8.8
| ASW | 35.1 | 57.9 | 7.0
| CHB | 26.5 | 50.7 | 22.8
| CHD | 30.3 | 44.0 | 25.7
| GIH | 11.9 | 39.6 | 48.5
| LWK | 52.7 | 38.2 | 9.1
| MEX | 8.6 | 36.2 | 55.2
| MKK | 42.9 | 42.3 | 14.7
| TSI | 6.9 | 38.2 | 54.9
| 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=0.000008
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7727656
|overall_frequency_n=70
|overall_frequency_d=128
|overall_frequency=0.546875
|n_genomes=42
|n_genomes_annotated=0
|n_haplomes=58
|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}}