{{Rsnum
|rsid=7914558
|Gene=CNNM2
|Chromosome=10
|position=104775908
|Orientation=plus
|GMAF=0.4293
|Gene_s=CNNM2
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 16.8 | 43.4 | 39.8
| HCB | 30.7 | 53.3 | 16.1
| JPT | 16.8 | 53.1 | 30.1
| YRI | 9.5 | 41.5 | 49.0
| ASW | 15.8 | 52.6 | 31.6
| CHB | 30.7 | 53.3 | 16.1
| CHD | 28.4 | 56.0 | 15.6
| GIH | 23.8 | 56.4 | 19.8
| LWK | 11.8 | 37.3 | 50.9
| MEX | 19.0 | 44.8 | 36.2
| MKK | 10.3 | 46.8 | 42.9
| TSI | 20.8 | 48.5 | 30.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21926974
|Trait=None
|Title=Genome-wide association study identifies five new schizophrenia loci.
|RiskAllele=G
|Pval=2E-8
|OR=1.2200
|ORtxt=[1.15-1.29]
|OA=1
}}

{{PMID Auto
|PMID=22520855
|Title=Association study of a new schizophrenia susceptibility locus of 10q24.32-33 in a Han Chinese population.
}}

{{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=2E-9
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{PMID Auto
|PMID=24160291
|Title=The impact of the genome-wide supported variant in the cyclin M2 gene on gray matter morphology in schizophrenia
|OA=1
}}

{{on chip | Illumina Human 1M}}