{{Rsnum
|rsid=11188352
|Gene=SORBS1
|Chromosome=10
|position=97301004
|Orientation=plus
|GMAF=0.09137
|Gene_s=SORBS1
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.0 | 8.1 | 91.9
| HCB | 0.0 | 9.3 | 90.7
| JPT | 0.0 | 13.2 | 86.8
| YRI | 9.8 | 27.9 | 62.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 9.3 | 90.7
| 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=3E-6
  |OR=.44
  |ORtxt=[0.25-0.62] unit increase
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}