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SNP information rs4149601

RS4149601

Normal allele: GG

Genetic variation in NEDD4L is associated with transverse and longitudinal blood pressure. Increases the risk of hypertension and adverse cardiovascular outcomes in patients with arterial hypertension treated with thiazide diuretics. Associated with favourable response to treatment with beta-blockers and diuretics in patients with arterial hypertension.

Polymorphism rs4149601 is related to topics like this:

Genetics and high blood pressure

Abnormally high blood pressure in the arteries, which transport blood from the heart to the rest of...


Research and publications:

  16788695   24-h ambulatory blood pressure is linked to chromosome 18q21-22 and genetic variation of NEDD4L associates with cross-sectional and longitudinal blood pressure in Swedes.

  17487281   Polymorphism in NEDD4L is associated with increased salt sensitivity, reduced levels of P-renin and increased levels of Nt-proANP.

  18268134   Expression, transcription, and possible antagonistic interaction of the human Nedd4L gene variant: implications for essential hypertension.

  18293164   Two polymorphisms in NEDD4L gene and essential hypertension in Chinese Hans - a population-based case-control study.

  18591455   Physiological interaction between alpha-adducin and WNK1-NEDD4L pathways on sodium-related blood pressure regulation.

  19156173   Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population.

  19635985   A functional variant of NEDD4L is associated with hypertension, antihypertensive response, and orthostatic hypotension.

  20003179   Genetic variation of NEDD4L is associated with essential hypertension in female Kazakh general population: a case-control study.

  20038744   Human Nedd4L rs4149601 G allele generates evolutionary new isoform I with C2 domain.

  21052022   A functional variant of the NEDD4L gene is associated with beneficial treatment response with β-blockers and diuretics in hypertensive patients.

  21058046   Genetics of salt-sensitive hypertension.

  21060895   Identification of candidate genes for dyslexia susceptibility on chromosome 18.

  21154329   [Association of the rs4149601 polymorphism of NEDD4L gene with obesity in Xinjiang Kazakh population].

  21573014   Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension.

  22992668   Pharmacogenomics knowledge for personalized medicine.

  23353631   Association of variants in NEDD4L with blood pressure response and adverse cardiovascular outcomes in hypertensive patients treated with thiazide diuretics.

  23549273   A functional variant of NEDD4L is associated with obesity and related phenotypes in a Han population of Southern China.

  24284497   Genetic variation in NEDD4L, an epithelial sodium channel regulator, is associated with cardiovascular disease and cardiovascular death.

  25098785   Genetic variation in NEDD4L, salt sensitivity, and hypertension: human NEDD4L rs4149601 G allele generates evolutionary new isoform I with C2 domain.

  25098786   Genetic variation in NEDD4L, salt sensitivity, and hypertension: human NEDD4L rs4149601 G allele generates evolutionary new isoform I with C2 domain.

  27103841   Personalized medicine and treatment approaches in hypertension: current perspectives.

  31993646   A Variant in the NEDD4L Gene Associates With Hypertension in Chronic Kidney Disease in the Southeastern Han Chinese Population.

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