{{Rsnum
|rsid=7397814
|Chromosome=12
|position=9394366
|Orientation=plus
|GMAF=0.1056
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LOC101930452
|Gene_s=LOC101930452
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 57.8 | 36.7 | 5.5
| HCB | 90.2 | 9.8 | 0.0
| JPT | 85.2 | 14.8 | 0.0
| YRI | 92.1 | 7.9 | 0.0
| ASW | 96.4 | 3.6 | 0.0
| CHB | 90.2 | 9.8 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 71.4 | 24.5 | 4.1
| LWK | 95.3 | 3.8 | 0.9
| MEX | 63.0 | 37.0 | 0.0
| MKK | 55.0 | 45.0 | 0.0
| TSI | 67.3 | 30.6 | 2.0
| 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=4E-6
  |OR=.19
  |ORtxt=[0.11-0.27] unit increase
  |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}}