rs11191580, NT5C2

N. diseases: 13
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
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
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.820 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
0.820 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
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
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
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
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
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.820 GeneticVariation GWASDB Genome-wide association study identifies five new schizophrenia loci. 21926974 2011
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.820 GeneticVariation GWASCAT Genome-wide association study identifies five new schizophrenia loci. 21926974 2011