{{Rsnum
|rsid=1747683
|Gene=SEPHS1
|Chromosome=10
|position=13361976
|Orientation=minus
|GMAF=0.4201
|Gene_s=SEPHS1
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 23.1 | 40.0 | 36.9
| HCB | 4.4 | 35.6 | 60.0
| JPT | 9.1 | 36.4 | 54.5
| YRI | 30.6 | 58.1 | 11.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 4.4 | 35.6 | 60.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 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=4E-7
  |OR=.16
  |ORtxt=[0.099-0.224] unit decrease
  |OA=1
}}