RNLS, renalase, FAD dependent amine oxidase, 55328

N. diseases: 32; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10887800
rs10887800
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C0032460
Disease:
Polycystic Ovary Syndrome
0.010 GeneticVariation BEFREE Similarly, Renalase rs10887800 AG/GG and G allele showed significant association with both infertility due to polycystic ovarian syndrome and unexplained infertility. 31579970 2019
dbSNP: rs2576178
rs2576178
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE Investigation of Renalase gene rs2576178 polymorphism in patients with coronary artery disease. 30181378 2018
dbSNP: rs10887800
rs10887800
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C0085207
Disease:
Gestational Diabetes
0.010 GeneticVariation BEFREE The variant rs10887800 showed an association with gestational diabetes mellitus and remained significant after multiple adjustments (p < 0.05), whereas rs2576178 showed weak association (p = 0.030) that was lost after multiple adjustments (p = 0.09). 27507673 2017
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0149721
Disease:
Left Ventricular Hypertrophy
0.010 GeneticVariation BEFREE The aim of this study was to test the association between a functional polymorphism Glu37Asp (rs2296545) of the renalase gene and left ventricular hypertrophy in a large cohort of patients with aortic stenosis. 29065134 2017
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0003507
Disease:
Aortic Valve Stenosis
0.010 GeneticVariation BEFREE In conclusion, we have found the association of the renalase Glu37Asp polymorphism with left ventricle hypertrophy in large group of females with aortic stenosis. 29065134 2017
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0149721
Disease:
Left Ventricular Hypertrophy
0.010 GeneticVariation BEFREE The aim of this study was to test the association between a functional polymorphism Glu37Asp (rs2296545) of the renalase gene and left ventricular hypertrophy in a large cohort of patients with aortic stenosis. 29065134 2017
dbSNP: rs2576178
rs2576178
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0085207
Disease:
Gestational Diabetes
0.010 GeneticVariation BEFREE The variant rs10887800 showed an association with gestational diabetes mellitus and remained significant after multiple adjustments (p < 0.05), whereas rs2576178 showed weak association (p = 0.030) that was lost after multiple adjustments (p = 0.09). 27507673 2017
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0264657
Disease:
Renal sclerosis with hypertension
0.010 GeneticVariation BEFREE Renalase gene (rs2296545) polymorphism was genotyped in 178 patients with CKD (83 normotensive and 95 hypertensive nephrosclerosis) and 178 normal healthy adults using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP). 25484193 2015
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C1561643
Disease:
Chronic Kidney Diseases
0.010 GeneticVariation BEFREE We found an association of renalase (rs2296545) CC genotype and C allele with CKD. 25484193 2015
dbSNP: rs10887800
rs10887800
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C0679403
Disease:
Vascular stenosis
0.010 GeneticVariation BEFREE The allele and the genotype of rs10887800 in the renalase gene were both associated with severe intracranial cerebral atherosclerotic vascular stenosis (p = 0.013 and p = 0.049, respectively). 24014100 2014
dbSNP: rs10887800
rs10887800
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C2316810
Disease:
Chronic kidney disease stage 5
0.010 GeneticVariation BEFREE Distribution of genotypes and frequencies of alleles of rs10887800 polymorphism were compared in the following subgroups of patients: ESRD HY + (n = 278) and ESRD HY - (n = 143). 21617193 2012
dbSNP: rs10887800
rs10887800
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.010 GeneticVariation BEFREE Distribution of genotypes and frequencies of alleles of rs10887800 polymorphism were compared in the following subgroups of patients: ESRD HY + (n = 278) and ESRD HY - (n = 143). 21617193 2012
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmö Diet and cancer study. 22812913 2012
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmö Diet and cancer study. 22812913 2012
dbSNP: rs2576178
rs2576178
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C2316810
Disease:
Chronic kidney disease stage 5
0.010 GeneticVariation BEFREE Genotype distribution and allele frequencies of rs2576178 polymorphism were compared in the following subgroups of patients: dialysed patients with hypertension: ESRD HY + (n = 200) and dialysed patients without hypertension: ESRD HY - (n = 169). 21617193 2012
dbSNP: rs2576178
rs2576178
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.010 GeneticVariation BEFREE Genotype distribution and allele frequencies of rs2576178 polymorphism were compared in the following subgroups of patients: dialysed patients with hypertension: ESRD HY + (n = 200) and dialysed patients without hypertension: ESRD HY - (n = 169). 21617193 2012
dbSNP: rs10887800
rs10887800
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C0011847
Disease:
Diabetes
0.010 GeneticVariation BEFREE The most interesting result is a strong association of the rs10887800 polymorphism with stroke in patients with and without diabetes. 21964580 2011
dbSNP: rs10887800
rs10887800
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C0011849
Disease:
Diabetes Mellitus
0.010 GeneticVariation BEFREE The most interesting result is a strong association of the rs10887800 polymorphism with stroke in patients with and without diabetes. 21964580 2011
dbSNP: rs10887800
rs10887800
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE The most interesting result is a strong association of the rs10887800 polymorphism with stroke in patients with and without diabetes. 21964580 2011
dbSNP: rs2114406
rs2114406
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C0085580
Disease:
Essential Hypertension
0.010 GeneticVariation BEFREE By single locus analyses, three SNPs, rs2576178, rs2296545, and rs2114406, showed significant associations with EH (P < 0.05). 17216203 2007
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0085580
Disease:
Essential Hypertension
0.010 GeneticVariation BEFREE After Bonferroni correction for multiple comparisons, the associations of rs2576178 and rs2296545 with EH were still significant in stage 2. 17216203 2007
dbSNP: rs2576178
rs2576178
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0085580
Disease:
Essential Hypertension
0.010 GeneticVariation BEFREE After Bonferroni correction for multiple comparisons, the associations of rs2576178 and rs2296545 with EH were still significant in stage 2. 17216203 2007
dbSNP: rs10887800
rs10887800
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C0020538
Disease:
Hypertensive disease
0.020 GeneticVariation BEFREE Furthermore, no significant differences were obtained in the risk or protective effects of renalase rs10887800 SNP against hypertension and/or CAD in both recessive and dominant genetic models (P > 0.05). 30548657 2019
dbSNP: rs10887800
rs10887800
Entrez Id: 55328;101929727
Gene Symbol: RNLS;LOC101929727
RNLS;LOC101929727
CUI: C1956346
Disease:
Coronary Artery Disease
0.020 GeneticVariation BEFREE Furthermore, no significant differences were obtained in the risk or protective effects of renalase rs10887800 SNP against hypertension and/or CAD in both recessive and dominant genetic models (P > 0.05). 30548657 2019
dbSNP: rs2576178
rs2576178
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C1956346
Disease:
Coronary Artery Disease
0.020 GeneticVariation BEFREE In summary, Renalase rs2576178 polymorphism is associated with increased risk of CAD, but this finding should be confirmed by larger studies with more diverse ethnic populations. 30181378 2018