SNP information rs2230500
Normal allele: GG
SNP 1425G/A in PRKCH is associated with ischaemic stroke and cerebral haemorrhage.
Polymorphism rs2230500 is related to topics like this:
Ischemic stroke has a multifactorial etiology, with genetic causes playing a significant role,...
Research and publications:
17206144 A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction.
18164711 Association between PRKCH gene polymorphisms and subcortical silent brain infarction.
19069168 [Genetic risk factors of ischemic stroke identified by a genome-wide association study].
19703523 Association of PRKCH gene with lacunar infarction in a local Chinese Han population.
20602195 PRKCH gene polymorphism is associated with the risk of severe gastric atrophy.
21358133 [Genome-wide association study for ischemic stroke based on the Hisayama study].
27796860 Genetic Risk Factors for Ischemic and Hemorrhagic Stroke.
28640647 Influence of PRKCH gene polymorphism on antihypertensive response to amlodipine and telmisartan.
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