{{Rsnum
|rsid=2186369
|Gene=SMARCB1
|Chromosome=22
|position=23828809
|Orientation=plus
|GMAF=0.1465
|Gene_s=SMARCB1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.0 | 33.9 | 66.1
| HCB | 0.0 | 2.3 | 97.7
| JPT | 0.0 | 6.8 | 93.2
| YRI | 0.0 | 58.3 | 41.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 2.3 | 97.7
| 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-13
  |OR=.30
  |ORtxt=[0.22-0.39] unit decrease
  |OA=1
}}