Normal allele: AA
The polymorphism is associated with increased plasma homocysteine and increased risk of hypertension.
Polymorphism rs17367504 is related to topics like this:
Research and publications:
19430479 Genome-wide association study of blood pressure and hypertension.
19430483 Genome-wide association study identifies eight loci associated with blood pressure.
19944404 Genomic dissection of population substructure of Han Chinese and its implication in association studies.
20224392 Blood pressure and human genetic variation in the general population.
20425154 Genome-wide association studies: contribution of genomics to understanding blood pressure and essential hypertension.
20852445 Common variants in or near FGF5, CYP17A1 and MTHFR genes are associated with blood pressure and hypertension in Chinese Hans.
20948529 Recent findings in the genetics of blood pressure and hypertension traits.
21060006 Genetic architecture of ambulatory blood pressure in the general population: insights from cardiovascular gene-centric array.
21129164 The genetics of blood pressure and hypertension: the role of rare variation.
21613384 Methylenetetrahydrofolate reductase (MTHFR) polymorphism A1298C (Glu429Ala) predicts decline in renal function over time in the African-American Study of Kidney Disease and Hypertension (AASK) Trial and Veterans Affairs Hypertension Cohort (VAHC
21860704 Implications of discoveries from genome-wide association studies in current cardiovascular practice.
21909115 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
22025373 Genetic variants and blood pressure in a population-based cohort: the Cardiovascular Risk in Young Finns study.
22100073 Blood pressure loci identified with a gene-centric array.
22504314 Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
22525200 Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
22856873 Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.
22959498 Recapitulation of four hypertension susceptibility genes (CSK, CYP17A1, MTHFR, and FGF5) in East Asians.
23049672 Top Three Pharmacogenomics and Personalized Medicine Applications at the Nexus of Renal Pathophysiology and Cardiovascular Medicine.
23133444 Genetic variation in CYP17A1 is associated with arterial stiffness in diabetic subjects.
23205182 A genome-wide association study of variations in maternal cardiometabolic genes and risk of placental abruption.
26658788 Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk.
27480026 Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension.
27736895 Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans.
27755385 The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia.
28425437 Are genetic polymorphisms in the renin-angiotensin-aldosterone system associated with essential hypertension? Evidence from genome-wide association studies.
28739976 Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.
29045471 Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.
30119983 The association between genetic risk score and blood pressure is modified by coffee consumption: Gene-diet interaction analysis in a population-based study.
31469255 A genome-wide association and replication study of blood pressure in Ugandan early adolescents.
35800018 Association Between MTHFR rs17367504 Polymorphism and Major Depressive Disorder in Taiwan: Evidence for Effect Modification by Exercise Habits.