{{Rsnum
|rsid=4684059
|Gene=HRH1
|Chromosome=3
|position=11191093
|Orientation=plus
|GMAF=0.3489
|Gene_s=HRH1
|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 | 14.2 | 49.6 | 36.3
| HCB | 19.0 | 58.4 | 22.6
| JPT | 15.9 | 55.8 | 28.3
| YRI | 2.0 | 32.0 | 66.0
| ASW | 8.8 | 28.1 | 63.2
| CHB | 19.0 | 58.4 | 22.6
| CHD | 15.6 | 43.1 | 41.3
| GIH | 8.9 | 33.7 | 57.4
| LWK | 10.0 | 40.0 | 50.0
| MEX | 6.9 | 25.9 | 67.2
| MKK | 5.8 | 34.6 | 59.6
| TSI | 11.8 | 39.2 | 49.0
| 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=8E-6
  |OR=.17
  |ORtxt=[0.095-0.243] unit increase
  |OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA}}