Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10494366
rs10494366
NOS1AP ; LOC105371475
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 GeneticVariation GWASDB A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. 16648850

2006
dbSNP: rs12029454
rs12029454
NOS1AP ; LOC105371475
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
dbSNP: rs12029454
rs12029454
NOS1AP ; LOC105371475
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		A 0.800 GeneticVariation GWASDB Common variants at ten loci influence QT interval duration in the QTGEN Study. 19305408

2009
dbSNP: rs16857031
rs16857031
NOS1AP ; LOC105371475
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		G 0.800 GeneticVariation GWASDB Common variants at ten loci influence QT interval duration in the QTGEN Study. 19305408

2009
dbSNP: rs3934467
rs3934467
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
dbSNP: rs4657175
rs4657175
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
dbSNP: rs4657175
rs4657175
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 GeneticVariation GWASDB A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval. 22726844

2012
dbSNP: rs4657178
rs4657178
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		T 0.800 GeneticVariation GWASDB Common variants at ten loci modulate the QT interval duration in the QTSCD Study. 19305409

2009
dbSNP: rs10127719
rs10127719
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
dbSNP: rs10800352
rs10800352
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
dbSNP: rs10918602
rs10918602
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
dbSNP: rs10918796
rs10918796
NOS1AP ; LOC105371475
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 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
dbSNP: rs10919021
rs10919021
NOS1AP
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
dbSNP: rs11805598
rs11805598
NOS1AP ; LOC105371475
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 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
dbSNP: rs12027785
rs12027785
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
dbSNP: rs12116744
rs12116744
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
dbSNP: rs12123267
rs12123267
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
dbSNP: rs12135795
rs12135795
NOS1AP
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 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
dbSNP: rs12567315
rs12567315
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209

2012
dbSNP: rs12724220
rs12724220
NOS1AP
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 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
dbSNP: rs12734991
rs12734991
NOS1AP
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 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
dbSNP: rs1337068
rs1337068
NOS1AP ; LOC105371475
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
dbSNP: rs1510291
rs1510291
NOS1AP
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
dbSNP: rs1510291
rs1510291
NOS1AP
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
dbSNP: rs16860953
rs16860953
NOS1AP
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012