{{Rsnum
|rsid=5757676
|Chromosome=22
|position=39445695
|Orientation=plus
|GMAF=0.09826
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MGAT3
|Gene_s=MGAT3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 64.6 | 31.9 | 3.5
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 89.5 | 10.5 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 86.1 | 13.9 | 0.0
| LWK | 96.4 | 3.6 | 0.0
| MEX | 84.5 | 15.5 | 0.0
| MKK | 87.8 | 12.2 | 0.0
| TSI | 55.9 | 40.2 | 3.9
| 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=1E-7
  |OR=.20
  |ORtxt=[0.12-0.27] unit decrease
  |OA=1
}}

{{on chip | Illumina Human 1M}}