{{Rsnum
|rsid=6881634
|Chromosome=5
|position=78335030
|Orientation=plus
|GMAF=0.3705
|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 | 30.1 | 54.9 | 15.0
| HCB | 1.5 | 8.1 | 90.4
| JPT | 0.9 | 14.2 | 85.0
| YRI | 3.4 | 34.7 | 61.9
| ASW | 10.5 | 45.6 | 43.9
| CHB | 1.5 | 8.1 | 90.4
| CHD | 0.9 | 14.8 | 84.3
| GIH | 18.8 | 52.5 | 28.7
| LWK | 4.5 | 41.8 | 53.6
| MEX | 12.1 | 37.9 | 50.0
| MKK | 16.0 | 41.0 | 42.9
| TSI | 47.1 | 41.2 | 11.8
| 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=rs6881634
|overall_frequency_n=51
|overall_frequency_d=128
|overall_frequency=0.398438
|n_genomes=31
|n_genomes_annotated=0
|n_haplomes=41
|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}}