DisGeNET - a database of gene-disease associations

Variant: rs10127719 ×

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:

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.

2012