{{Rsnum
|rsid=459482
|Gene=MX1
|Chromosome=21
|position=41421864
|Orientation=plus
|GMAF=0.4747
|Gene_s=MX1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 42.2 | 45.3 | 12.5
| HCB | 13.3 | 53.3 | 33.3
| JPT | 9.1 | 61.4 | 29.5
| YRI | 28.6 | 47.6 | 23.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 13.3 | 53.3 | 33.3
| 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=C
  |Pval=2E-6
  |OR=.15
  |ORtxt=[0.089-0.213] unit decrease
  |OA=1
}}