{{Rsnum
|rsid=4076555
|Gene=SYT9
|Chromosome=11
|position=7443141
|Orientation=minus
|GMAF=0.3889
|Gene_s=RPL35AP29,SYT9
|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 | 52.2 | 39.8 | 8.0
| HCB | 56.6 | 36.8 | 6.6
| JPT | 68.1 | 28.3 | 3.5
| YRI | 6.8 | 28.6 | 64.6
| ASW | 12.3 | 49.1 | 38.6
| CHB | 56.6 | 36.8 | 6.6
| CHD | 56.1 | 35.5 | 8.4
| GIH | 62.4 | 31.7 | 5.9
| LWK | 5.5 | 27.3 | 67.3
| MEX | 58.6 | 36.2 | 5.2
| MKK | 13.5 | 48.7 | 37.8
| TSI | 46.5 | 46.5 | 6.9
| 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=C
  |Pval=7E-6
  |OR=.16
  |ORtxt=[0.09-0.229] unit decrease
  |OA=1
}}

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