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

SERPINE1

Gene name: serpin family E member 1
OMIM ID: 173360
Chromosome location: 7q22.1

Polymorphisms

Disease/PhenotypeIschemic stroke, susceptibility to
Reference transcriptNM_000602.4
DNA Changec.-820_-817G(4_5)
A.A. Change
Exon/Intron5' of the ATG codon
Variation Typeindel
Reference SNPrs587776796
Cases118 MI patients
Controls184 healthy controls
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
5G86 (36,45%)195 (52,98%)1
4G150 (63,55%)173 (47,02%)1,96 (1,4-2,72)0.03
5G/5G9 (7,64%)73 (39,68%)1
4G/5G68 (57,62%)49 (26,63%)11,2 (8,3-15,08)< 0.001
4G/4G41 (34,74%)62 (33,69%)5,36 (3,8-7,2)< 0.001
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.