rs7914558, CNNM2

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.830 GeneticVariation BEFREE We investigated the 10q24.32 locus and discovered a 339-bp <i>Alu</i> insertion polymorphism (rs71389983) in complete linkage disequilibrium (LD) with the schizophrenia GWAS risk variant rs7914558. 31840948 2020
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.830 GeneticVariation BEFREE Although the biological role of CNNM2 in schizophrenia remains unknown, these data suggest that this CNNM2 risk variant rs7914558 may have an impact on neural systems relevant to social cognition. 24311551 2014
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.830 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.830 GeneticVariation BEFREE Recently, a new schizophrenia susceptibility locus 10q24.32-q24.33, containing two single-nucleotide polymorphisms (SNPs: rs7914558 and rs11191580), was identified in a genome-wide association study. 22520855 2012
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.830 GeneticVariation GWASCAT Genome-wide association study identifies five new schizophrenia loci. 21926974 2011
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.830 GeneticVariation GWASDB Genome-wide association study identifies five new schizophrenia loci. 21926974 2011