{{Rsnum
|rsid=9886428
|Gene=SGCZ
|Chromosome=8
|position=14256307
|Orientation=plus
|GMAF=0.3292
|Gene_s=SGCZ
|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 | 26.1 | 43.2 | 30.6
| HCB | 6.8 | 39.4 | 53.8
| JPT | 6.4 | 38.2 | 55.5
| YRI | 2.8 | 25.9 | 71.3
| ASW | 5.3 | 35.1 | 59.6
| CHB | 6.8 | 39.4 | 53.8
| CHD | 7.6 | 41.0 | 51.4
| GIH | 8.0 | 37.0 | 55.0
| LWK | 2.8 | 24.1 | 73.1
| MEX | 7.0 | 54.4 | 38.6
| MKK | 7.2 | 41.2 | 51.6
| TSI | 30.7 | 49.5 | 19.8
| 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=3E-6
  |OR=.14
  |ORtxt=[0.083-0.203] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}