{{Rsnum
|rsid=11910494
|Gene=HUNK
|Chromosome=21
|position=31923801
|Orientation=plus
|GMAF=0.371
|Gene_s=HUNK
|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 | 38.1 | 50.4 | 11.5
| HCB | 67.2 | 27.0 | 5.8
| JPT | 61.6 | 33.0 | 5.4
| YRI | 13.0 | 34.2 | 52.7
| ASW | 5.4 | 50.0 | 44.6
| CHB | 67.2 | 27.0 | 5.8
| CHD | 55.0 | 40.4 | 4.6
| GIH | 42.6 | 43.6 | 13.9
| LWK | 6.4 | 31.2 | 62.4
| MEX | 60.3 | 31.0 | 8.6
| MKK | 18.1 | 52.3 | 29.7
| TSI | 42.2 | 49.0 | 8.8
| 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=8E-6
  |OR=.15
  |ORtxt=[0.083-0.213] unit increase
  |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}}