{{Rsnum
|rsid=11557467
|Gene=ZPBP2
|Chromosome=17
|position=39872381
|Orientation=plus
|GMAF=0.4068
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=ZPBP2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 21.4 | 55.4 | 23.2
| HCB | 44.9 | 45.6 | 9.6
| JPT | 52.7 | 39.3 | 8.0
| YRI | 58.3 | 31.7 | 10.0
| ASW | 44.6 | 33.9 | 21.4
| CHB | 44.9 | 45.6 | 9.6
| CHD | 53.7 | 39.8 | 6.5
| GIH | 41.6 | 43.6 | 14.9
| LWK | 60.6 | 29.4 | 10.1
| MEX | 34.5 | 48.3 | 17.2
| MKK | 66.7 | 30.8 | 2.6
| TSI | 25.5 | 53.9 | 20.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=21985515
|Title=Association of genetic variants in chromosome 17q21 and adult-onset asthma in a Chinese Han population
|OA=1
}}

{{PMID|19426955|OA=1
}} Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene.

{{PMID|19714205|OA=1
}} Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children.

{{PMID|19732864|OA=1
}} Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.

{{PMID|20639879|OA=1
}} Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis.

{{PMID|21506939}} Replicated association of 17q12-21 with susceptibility of primary biliary cirrhosis in a Japanese cohort.

{{GET Evidence
|gene=ZPBP2
|aa_change=Ser173Ile
|aa_change_short=S173I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11557467
|overall_frequency_n=4644
|overall_frequency_d=10758
|overall_frequency=0.431679
|n_genomes=28
|n_genomes_annotated=0
|n_haplomes=37
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.688
|nblosum100=5
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}