DisGeNET - a database of gene-disease associations

NOS1AP, nitric oxide synthase 1 adaptor protein, 9722

N. diseases: 85; N. variants: 60

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs10494366

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Genetic analyses of diverse populations improves discovery for complex traits.

31217584

2019

dbSNP:

rs12029454

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Genetic analyses of diverse populations improves discovery for complex traits.

31217584

2019

dbSNP:

rs16857031

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Genetic analyses of diverse populations improves discovery for complex traits.

31217584

2019

dbSNP:

rs3934467

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Genetic analyses of diverse populations improves discovery for complex traits.

31217584

2019

dbSNP:

rs4657175

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Genetic analyses of diverse populations improves discovery for complex traits.

31217584

2019

dbSNP:

rs4657178

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Genetic analyses of diverse populations improves discovery for complex traits.

31217584

2019

dbSNP:

rs3934467

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals.

29213071

2017

dbSNP:

rs16857031

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.

24952745

2014

dbSNP:

rs3934467

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.

24952745

2014

dbSNP:

rs12029454

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

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:

rs3934467

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

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

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

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:

rs4657175

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

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

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.

22726844

2012

dbSNP:

rs10494366

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Several common variants modulate heart rate, PR interval and QRS duration.

20062063

2010

dbSNP:

rs12029454

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASDB

Common variants at ten loci influence QT interval duration in the QTGEN Study.

19305408

2009

dbSNP:

rs12029454

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Common variants at ten loci influence QT interval duration in the QTGEN Study.

19305408

2009

dbSNP:

rs16857031

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASDB

Common variants at ten loci influence QT interval duration in the QTGEN Study.

19305408

2009

dbSNP:

rs16857031

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Common variants at ten loci influence QT interval duration in the QTGEN Study.

19305408

2009

dbSNP:

rs4657178

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

19305409

2009

dbSNP:

rs4657178

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASDB

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

19305409

2009

dbSNP:

rs10494366

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASDB

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.

16648850

2006

dbSNP:

rs10494366

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.800

GeneticVariation

GWASCAT

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.

16648850

2006

dbSNP:

rs1415259

Entrez Id:	9722;105371475
Gene Symbol:	NOS1AP;LOC105371475

NOS1AP;LOC105371475

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.700

GeneticVariation

GWASCAT

Genetic analyses of diverse populations improves discovery for complex traits.

31217584

2019

dbSNP:

rs4657172

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:

QT interval feature (observable entity)

0.700

GeneticVariation

GWASCAT

Genetic analyses of diverse populations improves discovery for complex traits.

31217584

2019