{{Rsnum
|rsid=1122979
|Gene=ABCF2
|Chromosome=7
|position=151217985
|Orientation=plus
|GMAF=0.06107
|Gene_s=ABCF2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 77.9 | 20.4 | 1.8
| HCB | 99.3 | 0.7 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 95.8 | 4.2 | 0.0
| ASW | 82.1 | 17.9 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 87.9 | 12.1 | 0.0
| LWK | 89.9 | 9.2 | 0.9
| MEX | 87.7 | 12.3 | 0.0
| MKK | 83.9 | 14.1 | 2.0
| TSI | 86.1 | 13.9 | 0.0
| 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=G
  |Pval=7E-6
  |OR=.22
  |ORtxt=[0.12-0.32] unit decrease
  |OA=1
}}

{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}