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.
20224392 Blood pressure and human genetic variation in the general population.
20948529 Recent findings in the genetics of blood pressure and hypertension traits.
21045733 Discovery and replication of new genetic loci for blood pressure in the Women's Genome Health Study.
21129164 The genetics of blood pressure and hypertension: the role of rare variation.
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.
22100073 Blood pressure loci identified with a gene-centric array.
22856873 Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.
23133444 Genetic variation in CYP17A1 is associated with arterial stiffness in diabetic subjects.
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.
31469255 A genome-wide association and replication study of blood pressure in Ugandan early adolescents.