{{Rsnum
|rsid=9857275
|Gene=ZBTB38
|Chromosome=3
|position=141359346
|Orientation=plus
|GMAF=0.1951
|Gene_s=ZBTB38
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 10.6 | 36.3 | 53.1
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 6.8 | 29.9 | 63.3
| ASW | 5.3 | 47.4 | 47.4
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 5.0 | 28.7 | 66.3
| LWK | 3.6 | 30.0 | 66.4
| MEX | 5.2 | 27.6 | 67.2
| MKK | 2.6 | 30.8 | 66.7
| TSI | 3.9 | 36.3 | 59.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22210626
|Trait=None
|Title=Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
|RiskAllele=
|Pval=0.000002
|OR=1.2800
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}