Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1137933
rs1137933
0.020 GeneticVariation BEFREE CT genotype of rs1137933C/T was significantly associated with increased risk of T2D (<i>P</i><0.0001). 30581791

2018

dbSNP: rs1137933
rs1137933
0.020 GeneticVariation BEFREE CT genotype and C allele of NOS2 rs1137933 C/T polymorphism were associated with a higher risk of T2D, and no association was observed between T allele of NOS2 rs2779248 T/C polymorphism and T2D while TC genotype of this SNP decreased the risk of T2D in the study participants. 30581791

2018

dbSNP: rs2779248
rs2779248
0.020 GeneticVariation BEFREE CT genotype and C allele of NOS2 rs1137933 C/T polymorphism were associated with a higher risk of T2D, and no association was observed between T allele of NOS2 rs2779248 T/C polymorphism and T2D while TC genotype of this SNP decreased the risk of T2D in the study participants. 30581791

2018

dbSNP: rs2779248
rs2779248
0.020 GeneticVariation BEFREE Nitric Oxide Synthase 2 Polymorphisms (rs2779248T/C and rs1137933C/T) and the Risk of Type 2 Diabetes in Zahedan, Southeastern Iran. 30581791

2018

dbSNP: rs1137933
rs1137933
0.020 GeneticVariation BEFREE These preliminary findings indicate that the NOS2 rs2779248, NOS2 rs1137933, and NOS3 rs3918188 genetic polymorphisms are potentially related to the susceptibility to T2DM, and the rs1800783 polymorphism might be considered as genetic risk factors for diabetic nephropathy, and family history of diabetes was closely associated with rs11771443 polymorphism in DN, and the genetic variants might be used as molecular markers for evaluating the risk of T2DM and diabetic nephropathy.© 2016 IUBMB Life, 68(7):516-525, 2016. 27192959

2016

dbSNP: rs2779248
rs2779248
0.020 GeneticVariation BEFREE These preliminary findings indicate that the NOS2 rs2779248, NOS2 rs1137933, and NOS3 rs3918188 genetic polymorphisms are potentially related to the susceptibility to T2DM, and the rs1800783 polymorphism might be considered as genetic risk factors for diabetic nephropathy, and family history of diabetes was closely associated with rs11771443 polymorphism in DN, and the genetic variants might be used as molecular markers for evaluating the risk of T2DM and diabetic nephropathy.© 2016 IUBMB Life, 68(7):516-525, 2016. 27192959

2016