Disease A B C D E F G H I J K L M N O P Q R S T U V W X Y Z [0-9]
Gene A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

NOS3

Gene name: nitric oxide synthase 3 (endothelial cell)
OMIM ID: 163729
Chromosome location: 7q36.1

Polymorphisms

Disease/PhenotypeIschemic stroke, susceptibility to
Reference transcriptNM_000603.4
DNA Changec.894T>G
A.A. Changep.Asp298Glu
Exon/Intronexon 8
Variation Typesubstitution
Reference SNPrs1799983
Cases165
Controls182
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
G70.3%80.2%1
T29.7%19.8%1.71 (1.21-2.43) 0.003
GG50.3%64.3%1
GT40.0%31.9%1.60 (1.02-2.52)0.040
TT8.0%3.8%3.22 (1.27-8.18)0.014
GT + TT46.7%35.7%1.78 (1.16-2.73)0.009
ReferenceDiakite B, Hamzi K, Slassi I, El Yahyaoui M, El Alaoui MM, Habbal R, Sellama N; GMRAVC.G894T endothelial nitric oxide synthase polymorphism and ischemic stroke in Morocco.
Meta Gene. 2014 May 7;2:349-57.

Disease/PhenotypeIschemic stroke, susceptibility to
Reference transcriptNM_000603.4
DNA Changec.894T>G
A.A. Changep.Asp298Glu
Exon/Intronexon 8
Variation Typesubstitution
Reference SNPrs1799983
Cases118 MI patients
Controls184 healthy controls
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
T170 (72,03%)294 (79,89%)1
G66 (27,97%)74 (20,11%)1.54 (1.06-2.23)0.001
TT60 (50,85%)116 (63,04%)1
TG50 (42,37%)62 (33,69%)1,55 (0,97-2,48)0,02
GG8 (6,78%)6 (3,27%)2,57 (0,87-7,52)0,01
ReferenceHassani Idrissi H, Hmimech W, Diakite B, Korchi F, Baghdadi D, Habbal R, Nadifi S. Association of G894T eNOS, 4G/5G PAI and T1131C APOA5 polymorphisms with susceptibility to myocardial infarction in Morocco.
Meta Gene. 2016 Apr 3;9:56-61. doi: 10.1016/j.mgene.2016.03.004. eCollection 2016.