{{Rsnum
|rsid=12530
|Gene=RTCB
|Chromosome=22
|position=32387917
|Orientation=plus
|GMAF=0.07117
|Gene_s=RTCB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 3.5 | 30.1 | 66.4
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 1.8 | 14.0 | 84.2
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 1.0 | 13.9 | 85.1
| LWK | 0.0 | 0.0 | 0.0
| MEX | 1.7 | 12.1 | 86.2
| MKK | 0.0 | 4.6 | 95.4
| TSI | 3.9 | 19.6 | 76.5
| 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=3E-6
  |OR=.18
  |ORtxt=[0.11-0.26] unit increase
  |OA=1
}}

{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}