{{Rsnum
|rsid=11994937
|Gene=NSMAF
|Chromosome=8
|position=58596021
|Orientation=plus
|GMAF=0.0427
|Gene_s=NSMAF
|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 | 92.7 | 7.3 | 0.0
| HCB | 81.8 | 18.2 | 0.0
| JPT | 91.8 | 8.2 | 0.0
| YRI | 86.6 | 13.4 | 0.0
| ASW | 83.9 | 16.1 | 0.0
| CHB | 81.8 | 18.2 | 0.0
| CHD | 74.1 | 25.0 | 0.9
| GIH | 94.9 | 5.1 | 0.0
| LWK | 82.6 | 17.4 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 89.6 | 10.4 | 0.0
| TSI | 99.0 | 1.0 | 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=C
  |Pval=5E-6
  |OR=.50
  |ORtxt=[0.29-0.72] 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}}