{{Rsnum
|rsid=2270788
|Gene=ABCB9
|Chromosome=12
|position=122929802
|Orientation=minus
|GMAF=0.2567
|Gene_s=ABCB9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 80.5 | 17.7 | 1.8
| HCB | 57.4 | 33.8 | 8.8
| JPT | 69.0 | 24.8 | 6.2
| YRI | 11.0 | 42.8 | 46.2
| ASW | 15.8 | 50.9 | 33.3
| CHB | 57.4 | 33.8 | 8.8
| CHD | 60.4 | 35.8 | 3.8
| GIH | 75.2 | 24.8 | 0.0
| LWK | 8.3 | 38.9 | 52.8
| MEX | 75.9 | 20.7 | 3.4
| MKK | 18.5 | 40.4 | 41.1
| TSI | 83.3 | 15.7 | 1.0
| 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=C
  |Pval=7E-6
  |OR=.24
  |ORtxt=[0.13-0.34] unit increase
  |OA=1
}}

{{on chip | 23andMe v1}}
{{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}}