{{Rsnum
|rsid=4875857
|Gene=CSMD1
|Chromosome=8
|position=2962287
|Orientation=plus
|GMAF=0.3081
|Gene_s=CSMD1
|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 | 5.3 | 29.2 | 65.5
| HCB | 5.1 | 39.4 | 55.5
| JPT | 7.1 | 41.6 | 51.3
| YRI | 41.5 | 42.9 | 15.6
| ASW | 33.3 | 54.4 | 12.3
| CHB | 5.1 | 39.4 | 55.5
| CHD | 7.5 | 37.4 | 55.1
| GIH | 1.0 | 21.8 | 77.2
| LWK | 33.6 | 50.9 | 15.5
| MEX | 3.4 | 22.4 | 74.1
| MKK | 26.3 | 45.5 | 28.2
| TSI | 2.9 | 28.4 | 68.6
| 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=5E-6
  |OR=.18
  |ORtxt=[0.11-0.26] unit increase
  |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}}