Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.500 GeneticVariation GWASDB Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms. 23212062

2012
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.100 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.100 GeneticVariation GWASDB A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval. 22726844

2012
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.100 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479

2011
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.100 GeneticVariation GWASDB Common variants at ten loci modulate the QT interval duration in the QTSCD Study. 19305409

2009
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.100 GeneticVariation GWASDB Common variants at ten loci influence QT interval duration in the QTGEN Study. 19305408

2009
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.100 GeneticVariation GWASDB A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. 16648850

2006