{{Rsnum
|rsid=10781380
|Gene=PRUNE2
|Chromosome=9
|position=76793228
|Orientation=plus
|GMAF=0.3269
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PRUNE2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.9 | 38.4 | 52.7
| HCB | 5.1 | 44.1 | 50.7
| JPT | 5.4 | 33.0 | 61.6
| YRI | 24.7 | 60.3 | 15.1
| ASW | 26.3 | 56.1 | 17.5
| CHB | 5.1 | 44.1 | 50.7
| CHD | 11.9 | 49.5 | 38.5
| GIH | 12.9 | 47.5 | 39.6
| LWK | 31.8 | 53.6 | 14.5
| MEX | 8.6 | 31.0 | 60.3
| MKK | 23.7 | 48.1 | 28.2
| TSI | 6.9 | 45.1 | 48.0
| 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=7E-7
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10781380
|overall_frequency_n=44
|overall_frequency_d=128
|overall_frequency=0.34375
|n_genomes=31
|n_genomes_annotated=0
|n_haplomes=40
|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}}