Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs548181
rs548181
Entrez Id: 3703;9638;105369550
Gene Symbol: STT3A;FEZ1;STT3A-AS1
STT3A;FEZ1;STT3A-AS1
CUI: C0036341
Disease:
Schizophrenia 		0.810 GeneticVariation BEFREE Finally, a meta-analysis was conducted comparing our data with data from the Schizophrenia Psychiatric Genome-Wide Association Study Consortium (PGC-SCZ) that supported rs548181 (p=1.39×10(-7)). 25579050 2015
dbSNP: rs548181
rs548181
Entrez Id: 3703;9638;105369550
Gene Symbol: STT3A;FEZ1;STT3A-AS1
STT3A;FEZ1;STT3A-AS1
CUI: C0036341
Disease:
Schizophrenia 		0.810 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs548181
rs548181
Entrez Id: 3703;9638;105369550
Gene Symbol: STT3A;FEZ1;STT3A-AS1
STT3A;FEZ1;STT3A-AS1
CUI: C0036341
Disease:
Schizophrenia 		G 0.810 GeneticVariation GWASDB Genome-wide association study identifies five new schizophrenia loci. 21926974 2011
dbSNP: rs548181
rs548181
Entrez Id: 3703;9638;105369550
Gene Symbol: STT3A;FEZ1;STT3A-AS1
STT3A;FEZ1;STT3A-AS1
CUI: C0036341
Disease:
Schizophrenia 		G 0.810 GeneticVariation GWASCAT Genome-wide association study identifies five new schizophrenia loci. 21926974 2011
dbSNP: rs548181
rs548181
Entrez Id: 3703;9638;105369550
Gene Symbol: STT3A;FEZ1;STT3A-AS1
STT3A;FEZ1;STT3A-AS1
CUI: C1263846
Disease:
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
dbSNP: rs548181
rs548181
Entrez Id: 3703;9638;105369550
Gene Symbol: STT3A;FEZ1;STT3A-AS1
STT3A;FEZ1;STT3A-AS1
CUI: C1263846
Disease:
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
dbSNP: rs587777216
rs587777216
Entrez Id: 3703
Gene Symbol: STT3A
STT3A
CUI: C3810062
Disease:
Congenital disorder of glycosylation type 1w 		0.800 GeneticVariation UNIPROT Mutations in STT3A and STT3B cause two congenital disorders of glycosylation. 23842455 2013
dbSNP: rs587777216
rs587777216
Entrez Id: 3703
Gene Symbol: STT3A
STT3A
CUI: C3810062
Disease:
Congenital disorder of glycosylation type 1w 		C 0.800 CausalMutation CLINVAR
dbSNP: rs548181
rs548181
Entrez Id: 3703;9638;105369550
Gene Symbol: STT3A;FEZ1;STT3A-AS1
STT3A;FEZ1;STT3A-AS1
CUI: C1269683
Disease:
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
dbSNP: rs548181
rs548181
Entrez Id: 3703;9638;105369550
Gene Symbol: STT3A;FEZ1;STT3A-AS1
STT3A;FEZ1;STT3A-AS1
CUI: C0005586
Disease:
Bipolar Disorder 		0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs548181
rs548181
Entrez Id: 3703;9638;105369550
Gene Symbol: STT3A;FEZ1;STT3A-AS1
STT3A;FEZ1;STT3A-AS1
CUI: C0008074
Disease:
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