{{Rsnum
|rsid=894177
|Gene=PBX2P1
|Chromosome=3
|position=143175569
|Orientation=plus
|GMAF=0.2452
|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 | 48.7 | 42.5 | 8.8
| HCB | 50.4 | 44.4 | 5.2
| JPT | 36.3 | 49.6 | 14.2
| YRI | 98.6 | 1.4 | 0.0
| ASW | 86.0 | 14.0 | 0.0
| CHB | 50.4 | 44.4 | 5.2
| CHD | 56.0 | 37.6 | 6.4
| GIH | 28.7 | 51.5 | 19.8
| LWK | 96.4 | 3.6 | 0.0
| MEX | 62.1 | 31.0 | 6.9
| MKK | 91.0 | 7.1 | 1.9
| TSI | 50.0 | 40.2 | 9.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20708005
|Trait=None
|Title=Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease
|RiskAllele=G
|Pval=0.000003
|OR=0.28
|ORtxt=[NR] unit decrease
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}