{{Rsnum
|rsid=137699
|Gene=SYNGR1
|Chromosome=22
|position=39352849
|Orientation=plus
|GMAF=0.3701
|Gene_s=SYNGR1
|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 | 4.6 | 41.5 | 53.8
| HCB | 4.4 | 26.7 | 68.9
| JPT | 0.0 | 16.3 | 83.7
| YRI | 81.0 | 19.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 4.4 | 26.7 | 68.9
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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=G
  |Pval=8E-6
  |OR=.16
  |ORtxt=[0.088-0.225] unit decrease
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}