rs1799983, NOS3

N. diseases: 246
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
0.020 GeneticVariation BEFREE The allele and genotype frequencies of the NOS3 polymorphism (rs1799983) were significantly different between subjects with de</span>ep vein thrombosis and control subjects. 23922896 2013
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
0.020 GeneticVariation BEFREE -922A/G shows both genotypic (P=0.0218; chi2=5.25; O.R=1.94) as well as allelic association (P=0.0014; chi2=10.19; O.R=2.0) while 894G/T shows only allelic (P=0.04; chi2=3.93; O.R=3.93) association with DVT. 20114041 2010