{{Rsnum
|rsid=1650123
|Gene=STAB2
|Chromosome=12
|position=103640541
|Orientation=plus
|GMAF=0.4132
|Gene_s=STAB2
|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 | 27.0 | 41.3 | 31.7
| HCB | 97.6 | 2.4 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 45.8 | 41.0 | 13.2
| ASW | 56.1 | 35.1 | 8.8
| CHB | 97.6 | 2.4 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 71.3 | 18.8 | 9.9
| LWK | 53.2 | 36.7 | 10.1
| MEX | 46.6 | 39.7 | 13.8
| MKK | 49.0 | 38.1 | 12.9
| TSI | 43.1 | 29.4 | 27.5
| 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=6E-6
  |OR=.15
  |ORtxt=[0.086-0.218] unit decrease
  |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}}