Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11191580
rs11191580
NT5C2
0.820 GeneticVariation BEFREE NT5C2 variant rs11191580 conferred susceptibility to SCZ and affected the clinical symptoms of SCZ in a South Chinese Han population. 27901213

2017
dbSNP: rs11191580
rs11191580
NT5C2
0.820 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013
dbSNP: rs11191580
rs11191580
NT5C2
0.820 GeneticVariation GWASDB Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. 22688191

2012
dbSNP: rs11191580
rs11191580
NT5C2
0.820 GeneticVariation GWASCAT Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. 22688191

2012
dbSNP: rs11191580
rs11191580
NT5C2
0.820 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
dbSNP: rs11191580
rs11191580
NT5C2
T 0.820 GeneticVariation GWASDB Genome-wide association study identifies five new schizophrenia loci. 21926974

2011
dbSNP: rs11191580
rs11191580
NT5C2
T 0.820 GeneticVariation GWASCAT Genome-wide association study identifies five new schizophrenia loci. 21926974

2011