Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1059004
rs1059004
Entrez Id: 10215
Gene Symbol: OLIG2
OLIG2
CUI: C0036341
Disease:
Schizophrenia
0.020 GeneticVariation BEFREE This result suggests that rs1059004 polymorphism and SZ have synergistic effects on brain connections. 31785364 2020
dbSNP: rs1059004
rs1059004
Entrez Id: 10215
Gene Symbol: OLIG2
OLIG2
CUI: C0036341
Disease:
Schizophrenia
0.020 GeneticVariation BEFREE We found that genetic polymorphisms in CNP (rs2070106) and OLIG2 (rs1059004 and rs9653711), previously associated with schizophrenia, predicted low expression of these genes. 17964117 2008
dbSNP: rs762178
rs762178
Entrez Id: 10215
Gene Symbol: OLIG2
OLIG2
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE The results provide further evidence that the SNP rs762178 in OLIG2 seems to be a potential candidate in altering risk for schizophrenia in the Chinese Han population and worthy of further replication and functional study. 17934761 2008
dbSNP: rs9653711
rs9653711
Entrez Id: 10215;107985505
Gene Symbol: OLIG2;LOC107985505
OLIG2;LOC107985505
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE We found that genetic polymorphisms in CNP (rs2070106) and OLIG2 (rs1059004 and rs9653711), previously associated with schizophrenia, predicted low expression of these genes. 17964117 2008