{{Rsnum
|rsid=907092
|Gene=IKZF3
|Chromosome=17
|position=39766006
|Orientation=plus
|GMAF=0.3466
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=IKZF3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 22.1 | 53.1 | 24.8
| HCB | 11.7 | 42.3 | 46.0
| JPT | 10.6 | 47.8 | 41.6
| YRI | 0.7 | 12.9 | 86.4
| ASW | 8.8 | 38.6 | 52.6
| CHB | 11.7 | 42.3 | 46.0
| CHD | 7.3 | 41.3 | 51.4
| GIH | 13.9 | 43.6 | 42.6
| LWK | 0.0 | 20.9 | 79.1
| MEX | 19.0 | 39.7 | 41.4
| MKK | 1.3 | 16.0 | 82.7
| TSI | 19.6 | 49.0 | 31.4
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19458352
|Trait=Primary biliary cirrhosis
|Title=Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants
|RiskAllele=A
|Pval=0.000008
|OR=1.29
|ORtxt=[1.15-1.44]
|OA=1
}}

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

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs907092
|overall_frequency_n=3829
|overall_frequency_d=10758
|overall_frequency=0.355921
|n_genomes=26
|n_genomes_annotated=0
|n_haplomes=32
|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 | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}