Disease: QT interval feature (observable entity) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10127719
rs10127719
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0429028
Disease:
QT interval feature (observable entity) 		0.700 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209 2012