Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7914558
rs7914558
CNNM2
CUI: C0036341
Disease: Schizophrenia
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
dbSNP: rs7914558
rs7914558
CNNM2
CUI: C0036341
Disease: Schizophrenia
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
dbSNP: rs7914558
rs7914558
CNNM2
CUI: C0036341
Disease: Schizophrenia
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