{{Rsnum
|rsid=1373549
|Chromosome=12
|position=46092055
|Orientation=minus
|GMAF=0.3058
|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 | 29.2 | 54.0 | 16.8
| HCB | 58.4 | 35.0 | 6.6
| JPT | 56.6 | 41.6 | 1.8
| YRI | 61.0 | 37.0 | 2.1
| ASW | 52.6 | 40.4 | 7.0
| CHB | 58.4 | 35.0 | 6.6
| CHD | 56.9 | 36.7 | 6.4
| GIH | 40.6 | 44.6 | 14.9
| LWK | 61.8 | 36.4 | 1.8
| MEX | 53.4 | 43.1 | 3.4
| MKK | 62.8 | 32.1 | 5.1
| TSI | 37.3 | 41.2 | 21.6
| 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=rs1373549
|overall_frequency_n=85
|overall_frequency_d=128
|overall_frequency=0.664062
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=75
|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}}