{{Rsnum
|rsid=5764106
|Gene=PARVB
|Chromosome=22
|position=44165407
|Orientation=plus
|GMAF=0.4348
|Gene_s=PARVB
|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 | 31.9 | 64.6
| HCB | 46.7 | 41.6 | 11.7
| JPT | 65.5 | 31.0 | 3.5
| YRI | 19.0 | 59.9 | 21.1
| ASW | 19.3 | 42.1 | 38.6
| CHB | 46.7 | 41.6 | 11.7
| CHD | 56.0 | 36.7 | 7.3
| GIH | 10.9 | 37.6 | 51.5
| LWK | 34.5 | 52.7 | 12.7
| MEX | 8.6 | 36.2 | 55.2
| MKK | 33.5 | 47.1 | 19.4
| TSI | 1.0 | 35.3 | 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=C
  |Pval=5E-6
  |OR=.19
  |ORtxt=[0.11-0.27] 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}}