{{Rsnum
|rsid=10503253
|Gene=CSMD1
|Chromosome=8
|position=4323322
|Orientation=plus
|GMAF=0.1942
|Gene_s=CSMD1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 2.7 | 32.7 | 64.6
| HCB | 11.1 | 45.9 | 43.0
| JPT | 4.4 | 38.9 | 56.6
| YRI | 0.7 | 13.6 | 85.7
| ASW | 1.8 | 24.6 | 73.7
| CHB | 11.1 | 45.9 | 43.0
| CHD | 9.3 | 44.4 | 46.3
| GIH | 11.9 | 48.5 | 39.6
| LWK | 0.0 | 13.6 | 86.4
| MEX | 0.0 | 10.3 | 89.7
| MKK | 0.0 | 16.7 | 83.3
| TSI | 2.0 | 31.4 | 66.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21926974
|Trait=None
|Title=Genome-wide association study identifies five new schizophrenia loci.
|RiskAllele=A
|Pval=2E-8
|OR=1.1600
|ORtxt=[1.11-1.21]
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23453885
  |Trait=Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
  |Title=Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
  |RiskAllele=
  |Pval=4E-8
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{PMID Auto
|PMID=23839771
|Title=Neural effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253
}}

{{PMID Auto
|PMID=23320435
|Title=Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}