{{Rsnum
|rsid=12750249
|Gene=TMEM161B
|Chromosome=1
|position=94256104
|Orientation=plus
|GMAF=0.2236
|Gene_s=TMEM161B
|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 | 8.0 | 40.7 | 51.3
| HCB | 7.3 | 41.6 | 51.1
| JPT | 14.2 | 49.6 | 36.3
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 17.5 | 82.5
| CHB | 7.3 | 41.6 | 51.1
| CHD | 8.3 | 43.1 | 48.6
| GIH | 4.0 | 23.8 | 72.3
| LWK | 0.0 | 1.8 | 98.2
| MEX | 6.9 | 44.8 | 48.3
| MKK | 0.0 | 1.3 | 98.7
| TSI | 2.0 | 41.2 | 56.9
| 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=4E-6
  |OR=.17
  |ORtxt=[0.095-0.235] 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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}