{{Rsnum
|rsid=3793039
|Gene=COL19A1
|Chromosome=6
|position=70031317
|Orientation=plus
|GMAF=0.2617
|Gene_s=COL19A1
|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 | 51.8 | 42.9 | 5.4
| HCB | 85.4 | 13.9 | 0.7
| JPT | 87.6 | 11.5 | 0.9
| YRI | 26.4 | 48.6 | 25.0
| ASW | 24.6 | 59.6 | 15.8
| CHB | 85.4 | 13.9 | 0.7
| CHD | 89.0 | 11.0 | 0.0
| GIH | 60.4 | 33.7 | 5.9
| LWK | 24.1 | 45.4 | 30.6
| MEX | 62.1 | 34.5 | 3.4
| MKK | 12.4 | 54.9 | 32.7
| TSI | 41.2 | 49.0 | 9.8
| 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=2E-6
  |OR=.24
  |ORtxt=[0.14-0.34] unit increase
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}