rs1198588, None

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.810 GeneticVariation BEFREE Excitatory neurons derived from hiPSCs with CRISPR/Cas9-edited rs1198588 or a rare proximally located SZ risk variant showed altered MIR137 expression, dendrite arborization, and synapse maturation. 28803920 2017
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.810 GeneticVariation GWASCAT Genome-wide association analysis identifies 13 new risk loci for schizophrenia. 23974872 2013
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.810 GeneticVariation GWASDB Genome-wide association analysis identifies 13 new risk loci for schizophrenia. 23974872 2013
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.810 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
0.810 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
Psychotic symptom
CUI: C0871189
Disease: Psychotic symptom
0.010 GeneticVariation BEFREE Based on extant data linking MIR 137 gene with structural brain anomalies and functional brain activations in schizophrenia, we hypothesized that MIR137 risk variants rs1625579 and rs1198588 would be associated with reduced fractional anisotropy in frontostriatal brain regions, impaired neurocognitive functioning and worse psychotic symptoms in schizophrenia patients compared with healthy controls. 25921703 2015