{{Rsnum
|rsid=2073145
|Gene=ZBP1
|Chromosome=20
|position=57615578
|Orientation=minus
|GMAF=0.4233
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ZBP1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 52.2 | 38.1 | 9.7
| HCB | 56.2 | 37.2 | 6.6
| JPT | 50.4 | 39.8 | 9.7
| YRI | 0.7 | 28.6 | 70.7
| ASW | 3.5 | 36.8 | 59.6
| CHB | 56.2 | 37.2 | 6.6
| CHD | 59.6 | 30.3 | 10.1
| GIH | 77.2 | 19.8 | 3.0
| LWK | 5.5 | 29.1 | 65.5
| MEX | 46.6 | 43.1 | 10.3
| MKK | 19.2 | 48.1 | 32.7
| TSI | 35.3 | 55.9 | 8.8
| 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
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}