RNLS, renalase, FAD dependent amine oxidase, 55328

N. diseases: 32; N. variants: 12
Disease: Hypertensive disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0020538
Disease:
Hypertensive disease 		0.050 GeneticVariation BEFREE Renalase gene rs2296545 polymorphism is significantly associated with increased risk of HT, whereas rs2576178 polymorphism may not be associated with the susceptibility to HT. 27434211 2016
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0020538
Disease:
Hypertensive disease 		0.050 GeneticVariation BEFREE The allele C of rs2296545 may be a predisposing factor of hypertension and patients with CC genotype are susceptible to develop hypertension. 24821235 2014
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0020538
Disease:
Hypertensive disease 		0.050 GeneticVariation BEFREE The recessive model showed a strong association of rs2296545 with ischemic stroke patients in hypertension subgroups (OR = 1.927, 95 % CI = 1.012-3.669, p = 0.046). 23564542 2013
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0020538
Disease:
Hypertensive disease 		0.050 GeneticVariation BEFREE A significant interaction was found between the rs2296545 C > G and age with respect to BP/hypertension. 22812913 2012
dbSNP: rs2296545
rs2296545
Entrez Id: 55328;142910
Gene Symbol: RNLS;LIPJ
RNLS;LIPJ
CUI: C0020538
Disease:
Hypertensive disease 		0.050 GeneticVariation BEFREE The C allele of rs2296545 SNP was associated with hypertension (P < 0.01). 21964580 2011