Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799983
rs1799983
0.060 GeneticVariation BEFREE G894T and -786T/C polymorphisms were not associated with asthma susceptibility. 22966886

2012

dbSNP: rs1799983
rs1799983
0.060 GeneticVariation BEFREE We investigated the role of NOS1 -84 G-->A and NOS3 -786 T-->C, 894 G-->T and 27 base pair (bp) repeat polymorphisms in 125 patients suffering from asthma and/or rhinitis and monosensitized against Dermatophagoides pteronyssinus (Dpter) and 111 controls from Algeria. 18086269

2008

dbSNP: rs1799983
rs1799983
0.060 GeneticVariation BEFREE Two SNPs in the promoter (C-786T and C-691T), two variants in the introns (27-bp repeat in intron 4 and G11T in intron 23), and two others in the exons (C774T in exon 6 and G894T in exon 7) were genotyped in 610 subjects (asthma, n = 294; healthy controls, n = 316), and a case-control association study was conducted. 18486767

2008

dbSNP: rs1799983
rs1799983
0.060 GeneticVariation BEFREE NOS1 C5266T and NOS3 G894T were not associated with asthma, atopy or FeNO. 16238787

2005

dbSNP: rs1799983
rs1799983
0.060 GeneticVariation BEFREE We identified a strong association between a known functional NOS3 missense sequence variant in the endothelial nitric oxide gene (G894T) and FENO level in a cohort of subjects with asthma. 12738608

2003

dbSNP: rs1799983
rs1799983
0.060 GeneticVariation BEFREE The Glu298Asp variant was not associated with asthma and/or related atopic phenotypes in our study. 12190658

2002