{{Rsnum
|rsid=9308433
|Gene=SMYD2
|Chromosome=1
|position=214283666
|Orientation=plus
|GMAF=0.3237
|Gene_s=SMYD2
|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 | 14.2 | 47.8 | 38.1
| HCB | 0.0 | 11.8 | 88.2
| JPT | 0.0 | 9.0 | 91.0
| YRI | 35.6 | 54.8 | 9.6
| ASW | 33.9 | 58.9 | 7.1
| CHB | 0.0 | 11.8 | 88.2
| CHD | 0.9 | 11.9 | 87.2
| GIH | 16.0 | 49.0 | 35.0
| LWK | 26.6 | 53.2 | 20.2
| MEX | 8.8 | 36.8 | 54.4
| MKK | 20.0 | 47.1 | 32.9
| TSI | 12.9 | 49.5 | 37.6
| 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=4E-6
  |OR=.15
  |ORtxt=[0.084-0.207] unit decrease
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}