{{Rsnum
|rsid=3851357
|Gene=PLCH1
|Chromosome=3
|position=155549651
|Orientation=minus
|GMAF=0.1042
|Gene_s=PLCH1
|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 | 62.8 | 31.9 | 5.3
| HCB | 86.9 | 13.1 | 0.0
| JPT | 94.7 | 5.3 | 0.0
| YRI | 96.6 | 3.4 | 0.0
| ASW | 93.0 | 7.0 | 0.0
| CHB | 86.9 | 13.1 | 0.0
| CHD | 94.5 | 5.5 | 0.0
| GIH | 73.3 | 24.8 | 2.0
| LWK | 97.3 | 2.7 | 0.0
| MEX | 74.1 | 24.1 | 1.7
| MKK | 92.2 | 7.8 | 0.0
| TSI | 67.6 | 26.5 | 5.9
| 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=9E-6
  |OR=.18
  |ORtxt=[0.1-0.26] 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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}