APLN, apelin, 8862

N. diseases: 226; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56204867
rs56204867
Entrez Id: 8862
Gene Symbol: APLN
APLN
CUI: C0020538
Disease:
Hypertensive disease
0.020 GeneticVariation BEFREE This meta-analysis revealed that there was no correlation between apelin polymorphisms, rs3761581 and rs56204867, and the prevalence of hypertension. 30755060 2019
dbSNP: rs5975126
rs5975126
Entrez Id: 8862
Gene Symbol: APLN
APLN
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE All participants including 645 hypertensive patients and 362 normotensive controls were genotyped for 4 gene polymorphisms associated with hypertension susceptibility including Apelin (rs909656, rs5975126) and APJ (rs10501367, rs11544374). 29800734 2018
dbSNP: rs755559514
rs755559514
Entrez Id: 8862
Gene Symbol: APLN
APLN
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Although the functional role of the G212A polymorphism has not yet been identified, it is possible to hypothesize that the presence of the A allele may cause a gain in function of the apelin/APJ system associated with a lower risk of hypertension. 22109355 2012
dbSNP: rs909656
rs909656
Entrez Id: 8862
Gene Symbol: APLN
APLN
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE All participants including 645 hypertensive patients and 362 normotensive controls were genotyped for 4 gene polymorphisms associated with hypertension susceptibility including Apelin (rs909656, rs5975126) and APJ (rs10501367, rs11544374). 29800734 2018
dbSNP: rs3115757
rs3115757
Entrez Id: 8862
Gene Symbol: APLN
APLN
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Genotype screening of APLN rs3115757 variant in Egyptian women population reveals an association with obesity and insulin resistance. 26025696 2015