{{Rsnum
|rsid=17776120
|Gene=ST6GAL1
|Chromosome=3
|position=187014891
|Orientation=plus
|GMAF=0.3416
|Gene_s=ST6GAL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 13.3 | 41.6 | 45.1
| HCB | 13.9 | 46.7 | 39.4
| JPT | 18.6 | 45.1 | 36.3
| YRI | 0.0 | 16.3 | 83.7
| ASW | 7.0 | 28.1 | 64.9
| CHB | 13.9 | 46.7 | 39.4
| CHD | 14.7 | 56.0 | 29.4
| GIH | 11.9 | 41.6 | 46.5
| LWK | 0.0 | 18.2 | 81.8
| MEX | 19.0 | 60.3 | 20.7
| MKK | 0.0 | 25.6 | 74.4
| TSI | 12.7 | 46.1 | 41.2
| 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=2E-6
  |OR=.17
  |ORtxt=[0.097-0.234] unit decrease
  |OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}