{{Rsnum
|rsid=7781977
|Gene=IKZF1
|Chromosome=7
|position=50306538
|Orientation=plus
|GMAF=0.3535
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=IKZF1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 47.8 | 40.7 | 11.5
| HCB | 32.1 | 46.6 | 21.4
| JPT | 22.2 | 56.5 | 21.3
| YRI | 47.9 | 44.4 | 7.7
| ASW | 61.8 | 32.7 | 5.5
| CHB | 32.1 | 46.6 | 21.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 45.5 | 47.5 | 7.1
| LWK | 46.2 | 35.8 | 17.9
| MEX | 25.0 | 51.8 | 23.2
| MKK | 38.2 | 48.7 | 13.2
| TSI | 51.5 | 38.1 | 10.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=C
  |Pval=5E7
  |OR=.17
  |ORtxt=[0.1-0.23] unit increase
  |OA=1
}}

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