rs10887800
This is a intron variant variant in the RNLS gene.
▶ClinVar annotation
▶Research that mentions this SNP (2)
▶Atorvastatin and losartan may upregulate renalase activity in hypertension but not coronary artery diseases: The role of gene polymorphismAssociationN=286Hamed Akbari et al.(2019)· Journal of Cellular Biochemistry
This case-control study in 286 Iranian subjects (60 hypertensive, 71 with CAD+hypertension, 61 with CAD, 69 controls) investigated the association between renalase rs10887800 polymorphism and cardiovascular disease risk, and examined how atorvastatin, losartan, and captopril therapy affect renalase activity. Higher renalase activity was observed in hypertensive patients (136.18±15.63) versus CAD patients (76.15±16.78; P<0.001), but renalase rs10887800 showed no significant association with hypertension or CAD risk in either recessive or dominant genetic models (P>0.05). Atorvastatin and losartan therapy increased renalase activity in hypertensive patients with AG/GG genotypes but had no effect in CAD+hypertension patients.
▶Renalase gene is a novel susceptibility gene for essential hypertension: a two-stage association study in northern Han Chinese populationAssociationN=2,586Qi Zhao et al.(2007)· Journal of Molecular Medicine
This two-stage case-control study investigated the renalase gene (C10orf59) as a susceptibility gene for essential hypertension in 2,586 northern Han Chinese subjects. Two SNPs showed significant associations: rs2576178 (OR=1.58, 95% CI 1.25-2.00, P=0.0002) and rs2296545 (OR=1.61, 95% CI 1.26-2.04, P=0.0002), with the latter encoding the Asp37Glu amino acid change. Risk-associated haplotypes further confirmed the gene's association with hypertension.
About RNLS
Enables several functions, including NADH binding activity; epinephrine binding activity; and monoamine oxidase activity. Involved in negative regulation of blood pressure and negative regulation of heart rate. Located in extracellular region. Implicated in essential hypertension and hypertension. Biomarker of end stage renal disease. [provided by Alliance of Genome Resources, Jul 2025]
View all RNLS variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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