Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5443
rs5443
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux
0.020 GeneticVariation BEFREE (2) TT genotype polymorphism rs5443 GNB3 gene may be a protective factor for the improved renal function in patients with primary vesicoureteral reflux in patients with genotype CC or CT. 27988909

2017

dbSNP: rs5443
rs5443
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
0.010 GeneticVariation BEFREE GERD is associated with GNB3 C825T.The results for GERD subgroups support the hypothesis that enhanced perception of reflux events, as a consequence of the increased signal transduction upon GPCR activation associated with the 825T allele, underlies this association. 19174793

2009

dbSNP: rs5443
rs5443
CUI: C0020175
Disease: Hunger
Hunger
0.010 GeneticVariation BEFREE Hunger and mood during extended fasting are dependent on the GNB3 C825T polymorphism. 19420911

2009

dbSNP: rs5443
rs5443
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.040 GeneticVariation BEFREE C825T polymorphism in the G protein beta3 subunit gene (GNB3) has been associated with arterial hypertension, coronary artery disease and myocardial infarction. 10704626

2000

dbSNP: rs5443
rs5443
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 GeneticVariation BEFREE C825T polymorphism in the G protein beta3 subunit gene (GNB3) has been associated with arterial hypertension, coronary artery disease and myocardial infarction. 10704626

2000

dbSNP: rs5443
rs5443
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE C825T polymorphism in the G protein beta3 subunit gene (GNB3) has been associated with arterial hypertension, coronary artery disease and myocardial infarction. 10704626

2000

dbSNP: rs5443
rs5443
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.070 GeneticVariation BEFREE C825T polymorphism in the G protein beta3 subunit gene (GNB3) has been associated with arterial hypertension, coronary artery disease and myocardial infarction. 10704626

2000

dbSNP: rs5443
rs5443
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.010 GeneticVariation BEFREE C825T polymorphism of the G-protein beta3 subunit gene and atrial fibrillation: association of the TT genotype with a reduced risk for atrial fibrillation. 15389246

2004

dbSNP: rs5443
rs5443
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.100 GeneticVariation BEFREE A C825T polymorphism of a gene encoding the beta3 subunit of heterotrimeric G proteins (GNB3) was reported to be associated with several pathological conditions, such as hypertension and depressive disorder. 12075862

2002

dbSNP: rs5443
rs5443
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.060 GeneticVariation BEFREE A C825T polymorphism of a gene encoding the beta3 subunit of heterotrimeric G proteins (GNB3) was reported to be associated with several pathological conditions, such as hypertension and depressive disorder. 12075862

2002

dbSNP: rs5443
rs5443
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.100 GeneticVariation BEFREE A C825T polymorphism was identified in the gene encoding the G-protein beta3 subunit (GNB3), and an association of the T-allele with hypertension was demonstrated in several studies. 15037876

2004

dbSNP: rs5443
rs5443
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.060 GeneticVariation BEFREE A case-control association study (225 healthy adults and 188 outpatients with depression) was performed to establish Risk-Combined Genotype (RCG) of the studied variants (OXTR rs53576 and the functional Gβ3 subunit rs5443). 28499211

2017

dbSNP: rs5443
rs5443
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.050 GeneticVariation BEFREE A case-control association study (225 healthy adults and 188 outpatients with depression) was performed to establish Risk-Combined Genotype (RCG) of the studied variants (OXTR rs53576 and the functional Gβ3 subunit rs5443). 28499211

2017

dbSNP: rs5443
rs5443
CUI: C0344315
Disease: Depressed mood
Depressed mood
0.050 GeneticVariation BEFREE A case-control association study (225 healthy adults and 188 outpatients with depression) was performed to establish Risk-Combined Genotype (RCG) of the studied variants (OXTR rs53576 and the functional Gβ3 subunit rs5443). 28499211

2017

dbSNP: rs5443
rs5443
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.040 GeneticVariation BEFREE A case-control association study of the C825T polymorphism with diabetes using multiple logistic regression analysis showed a significant association of the genotypes TT+TC with an odds ratio of 0.62 (p=0.008) independent of age, gender, and BMI. 18656447

2008

dbSNP: rs5443
rs5443
CUI: C0011847
Disease: Diabetes
Diabetes
0.020 GeneticVariation BEFREE A case-control association study of the C825T polymorphism with diabetes using multiple logistic regression analysis showed a significant association of the genotypes TT+TC with an odds ratio of 0.62 (p=0.008) independent of age, gender, and BMI. 18656447

2008

dbSNP: rs5443
rs5443
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.100 GeneticVariation BEFREE A common C825T polymorphism in the gene GNB3, which encodes the beta 3 subunit of heterotrimeric G proteins, was identified in cell lines from patients with hypertension. 15660499

2005

dbSNP: rs5443
rs5443
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.060 GeneticVariation BEFREE A common 825C>T polymorphism in exon 10 of the gene for the beta-3 subunit of heterotrimeric G-proteins, GNB3, has been associated in some studies with traits of the metabolic syndrome as well as coronary artery disease (CAD), but these associations were refuted by other studies. 16908025

2007

dbSNP: rs5443
rs5443
CUI: C0746556
Disease: metabolic disturbance
metabolic disturbance
0.010 GeneticVariation BEFREE A longitudinal study of the association between the GNB3 C825T polymorphism and metabolic disturbance in bipolar II patients treated with valproate. 26856249

2017

dbSNP: rs5443
rs5443
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.100 GeneticVariation BEFREE A polymorphism (C825T) in exon 10 of the gene encoding the beta 3 subunit of heterotrimeric G proteins (GN beta 3) has recently been described, and the T allele was found to be associated with late-onset hypertension. 10200987

1999

dbSNP: rs5443
rs5443
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.100 GeneticVariation BEFREE A polymorphism (C825T) in the gene encoding the G protein beta3 subunit (GNB3) has recently been associated with hypertension and obesity in several populations. 12109775

2002

dbSNP: rs5443
rs5443
CUI: C0028754
Disease: Obesity
Obesity
0.100 GeneticVariation BEFREE A polymorphism (C825T) in the gene encoding the G protein beta3 subunit (GNB3) has recently been associated with hypertension and obesity in several populations. 12109775

2002

dbSNP: rs5443
rs5443
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.100 GeneticVariation BEFREE A recent study has revealed that a novel variant (C825T) in exon 10 of the gene encoding the beta3 subunit of heterotrimetric G proteins (GNB3) is a genetic factor predisposing to hypertension in Caucasians. 10701813

2000

dbSNP: rs5443
rs5443
CUI: C0018801
Disease: Heart failure
Heart failure
0.020 GeneticVariation BEFREE A total of 350 subjects enrolled in the genetic substudy (GRAHF [Genetic Risk Assessment of Heart Failure in African Americans]) were genotyped for the C825T polymorphism. 25306451

2014

dbSNP: rs5443
rs5443
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.020 GeneticVariation BEFREE A total of 350 subjects enrolled in the genetic substudy (GRAHF [Genetic Risk Assessment of Heart Failure in African Americans]) were genotyped for the C825T polymorphism. 25306451

2014