{{Rsnum
|rsid=6502557
|Gene=MPRIP
|Chromosome=17
|position=17057664
|Orientation=plus
|GMAF=0.1451
|Gene_s=MPRIP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.5 | 21.2 | 75.2
| HCB | 3.6 | 21.2 | 75.2
| JPT | 2.7 | 18.6 | 78.8
| YRI | 4.1 | 26.5 | 69.4
| ASW | 1.8 | 22.8 | 75.4
| CHB | 3.6 | 21.2 | 75.2
| CHD | 0.9 | 26.6 | 72.5
| GIH | 2.0 | 27.7 | 70.3
| LWK | 0.9 | 20.9 | 78.2
| MEX | 8.6 | 24.1 | 67.2
| MKK | 8.3 | 30.1 | 61.5
| TSI | 5.9 | 30.4 | 63.7
| 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=6E-6
  |OR=.22
  |ORtxt=[0.12-0.31] unit increase
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}