{{Rsnum
|rsid=7652995
|Gene=ST6GAL1
|Chromosome=3
|position=187005156
|Orientation=plus
|GMAF=0.1313
|Gene_s=ST6GAL1
|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 | 69.9 | 30.1 | 0.0
| HCB | 74.3 | 25.0 | 0.7
| JPT | 73.2 | 25.0 | 1.8
| YRI | 76.9 | 23.1 | 0.0
| ASW | 77.2 | 21.1 | 1.8
| CHB | 74.3 | 25.0 | 0.7
| CHD | 87.2 | 11.9 | 0.9
| GIH | 63.4 | 29.7 | 6.9
| LWK | 68.2 | 30.0 | 1.8
| MEX | 84.5 | 12.1 | 3.4
| MKK | 88.5 | 10.9 | 0.6
| TSI | 78.4 | 21.6 | 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-17
  |OR=.37
  |ORtxt=[0.28-0.45] unit decrease
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}