rs548181
STT3A;FEZ1;STT3A-AS1
Schizophrenia
0.810
GeneticVariation
BEFREE
Finally, a meta-analysis was conducted comparing our data with data from the Schizophrenia Psychiatric Genome-Wide Association Study Cons ortium (PGC-SCZ) that supported rs548181 (p=1.39×10(-7)).
25579050
2015
rs587777216
×
Entrez Id:
3703
Gene Symbol:
STT3A
STT3A
Congenital disorder of glycosylation type 1w
C
0.800
CausalMutation
CLINVAR
rs548181
STT3A;FEZ1;STT3A-AS1
Schizophrenia
G
0.810
GeneticVariation
GWASCAT
Genome-wide association study identifies five new schizophrenia loci.
21926974
2011
rs548181
STT3A;FEZ1;STT3A-AS1
Schizophrenia
0.810
GeneticVariation
GWASCAT
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
23453885
2013
rs548181
STT3A;FEZ1;STT3A-AS1
Attention deficit hyperactivity disorder
0.800
GeneticVariation
GWASCAT
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
23453885
2013
rs548181
STT3A;FEZ1;STT3A-AS1
Major Depressive Disorder
0.700
GeneticVariation
GWASCAT
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
23453885
2013
rs548181
STT3A;FEZ1;STT3A-AS1
Bipolar Disorder
0.700
GeneticVariation
GWASCAT
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
23453885
2013
rs548181
STT3A;FEZ1;STT3A-AS1
Child Development Disorders, Pervasive
0.700
GeneticVariation
GWASCAT
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
23453885
2013
rs548181
STT3A;FEZ1;STT3A-AS1
Schizophrenia
G
0.810
GeneticVariation
GWASDB
Genome-wide association study identifies five new schizophrenia loci.
21926974
2011
rs548181
STT3A;FEZ1;STT3A-AS1
Attention deficit hyperactivity disorder
0.800
GeneticVariation
GWASDB
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
23453885
2013
rs587777216
×
Entrez Id:
3703
Gene Symbol:
STT3A
STT3A
Congenital disorder of glycosylation type 1w
0.800
GeneticVariation
UNIPROT
Mutations in STT3A and STT3B cause two congenital disorders of glycosylation.
23842455
2013