{{Rsnum
|rsid=1888414
|Chromosome=21
|position=20405418
|Orientation=plus
|GMAF=0.3641
|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 | 35.4 | 49.6 | 15.0
| HCB | 54.7 | 32.8 | 12.4
| JPT | 64.6 | 28.3 | 7.1
| YRI | 36.3 | 52.1 | 11.6
| ASW | 45.6 | 38.6 | 15.8
| CHB | 54.7 | 32.8 | 12.4
| CHD | 60.6 | 35.8 | 3.7
| GIH | 55.4 | 38.6 | 5.9
| LWK | 46.8 | 41.3 | 11.9
| MEX | 17.5 | 40.4 | 42.1
| MKK | 38.1 | 49.7 | 12.3
| TSI | 44.6 | 44.6 | 10.9
| 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=2E-7
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1888414
|overall_frequency_n=77
|overall_frequency_d=128
|overall_frequency=0.601562
|n_genomes=45
|n_genomes_annotated=0
|n_haplomes=67
|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}}