{{Rsnum
|rsid=2239633
|Gene=CEBPE
|Chromosome=14
|position=23119848
|Orientation=minus
|GMAF=0.3848
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CEBPE
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 29.2 | 46.0 | 24.8
| HCB | 41.6 | 43.8 | 14.6
| JPT | 29.2 | 41.6 | 29.2
| YRI | 70.1 | 27.9 | 2.0
| ASW | 51.8 | 39.3 | 8.9
| CHB | 41.6 | 43.8 | 14.6
| CHD | 49.5 | 33.0 | 17.4
| GIH | 35.6 | 50.5 | 13.9
| LWK | 71.8 | 27.3 | 0.9
| MEX | 36.2 | 51.7 | 12.1
| MKK | 74.4 | 23.7 | 1.9
| TSI | 23.5 | 57.8 | 18.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19684604
|Trait=Acute lymphoblastic leukemia (childhood)
|Title=Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia
|RiskAllele=G
|Pval=3E-7
|OR=1.34
|ORtxt=[1.22-1.45]
}}

{{omim
|id=613065
|rsnum=2239633
}}

{{PMID Auto
|PMID=22422485
|Title=Genetic variants modify susceptibility to leukemia in infants: A Children's Oncology Group report
|OA=1
}}

{{PMID Auto
|PMID=20919861
|Title=Variation at 7p12.2 and 10q21.2 influences childhood acute lymphoblastic leukemia risk in the Thai population and may contribute to racial differences in leukemia incidence.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2239633
|overall_frequency_n=47
|overall_frequency_d=128
|overall_frequency=0.367188
|n_genomes=29
|n_genomes_annotated=0
|n_haplomes=35
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto
|PMID=24564228
|Title=ARID5B polymorphism confers an increased risk to acquire specific MLL rearrangements in early childhood leukemia
|OA=1
}}

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