Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2070106
rs2070106
CNP
0.050 GeneticVariation BEFREE Additionally, we found the loss-of-function allele of a myelin-specific gene (CNP rs2070106-AA) associated with catatonia in 2 independent schizophrenia cohorts and also associated with white matter hyperintensities in a general population sample. 29252214

2018

dbSNP: rs2070106
rs2070106
CNP
0.050 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: rs2070106
rs2070106
CNP
0.050 GeneticVariation BEFREE The A-allele of rs2070106 within the 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNP), an oligodendrocyte-related gene, was reported to show reduced expression compared with the G-allele, and proposed to be associated with schizophrenia. 18289148

2008

dbSNP: rs2070106
rs2070106
CNP
0.050 GeneticVariation BEFREE The CNP SNP (rs2070106) was potentially associated with schizophrenia (P=0.027). 18496213

2008

dbSNP: rs2070106
rs2070106
CNP
0.050 GeneticVariation BEFREE A synonymous genetic variation in the CNP gene, rs2070106, has recently been shown to be associated with schizophrenia in Caucasians. 17306456

2007