Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5443
rs5443
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.010 GeneticVariation BEFREE The polymorphisms rs2241766 and rs5443 were found to potentially be associated with GDM; moreover, a positive interaction was demonstrated between rs2241766 and age, and a negative interaction was demonstrated with weight gain of ≥10 kg before 24-week gestation. 29519182

2019

dbSNP: rs5443
rs5443
CUI: C0232493
Disease: Epigastric pain
Epigastric pain
0.010 GeneticVariation BEFREE In a subgroup analysis, only minor allele (T) in GNB3 825C>T was associated with an increased susceptibility to the epigastric pain syndrome subtype (OR = 1.34, 95% CI 1.10-1.63, <i>P</i> = 0.003). 31178907

2019

dbSNP: rs5443
rs5443
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
0.010 GeneticVariation BEFREE Unique to our study is the establishment of an association between CRS in this patient population and GNB3 SNP rs5443, a variation in an established G protein component downstream of bitterant receptor signal transduction. 31137020

2019

dbSNP: rs5443
rs5443
CUI: C0265706
Disease: Gastroschisis
Gastroschisis
0.010 GeneticVariation BEFREE The rs4961 (ADD1), rs5443 (GNB3), rs1042713, and rs1042714 (ADRB2) were significantly associated with gastroschisis. 29550988

2018

dbSNP: rs5443
rs5443
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 GeneticVariation BEFREE The current meta-analysis suggested that the GNB3 C825T polymorphism may contribute to increased risk of cancer, especially of thyroid carcinoma. 25536621

2018

dbSNP: rs5443
rs5443
CUI: C1848533
Disease: Ataxia with vitamin E deficiency
Ataxia with vitamin E deficiency
0.010 GeneticVariation BEFREE No study has assessed the possible involvement of endothelial nitric oxide synthase (eNOS) T-786C and G894T and G-protein β3 subunit (GNB3) C825T polymorphisms with susceptibility to diabetic vasculogenic erectile dysfunction (VED) in North African subjects. 30101547

2018

dbSNP: rs5443
rs5443
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 GeneticVariation BEFREE The current meta-analysis suggested that the GNB3 C825T polymorphism may contribute to increased risk of cancer, especially of thyroid carcinoma. 25536621

2018

dbSNP: rs5443
rs5443
CUI: C0236788
Disease: Bipolar II disorder
Bipolar II disorder
0.010 GeneticVariation BEFREE At baseline, the GNB3 C825T polymorphisms were associated with the triglyceride level (P=0.032) in BP-II patients. 26856249

2017

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: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder
0.010 GeneticVariation BEFREE This study was conducted to explore the possibility of association between the single-nucleotide polymorphisms rs6264 of <i>BDNF</i>, rs5443 of <i>GNB3</i>, and rs1801133 of <i>MTHFR</i>; the <i>In/Del</i> polymorphism of <i>ACE</i>; and the <i>ε2</i> allele of <i>APOE</i> and major depressive disorder (MDD) and recurrent depressive disorder (RDD) in an East Slavic population. 27994504

2016

dbSNP: rs5443
rs5443
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.010 GeneticVariation BEFREE GNB3 C825T Polymorphism and Myocardial Recovery in Peripartum Cardiomyopathy: Results of the Multicenter Investigations of Pregnancy-Associated Cardiomyopathy Study. 26915373

2016

dbSNP: rs5443
rs5443
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms
0.010 GeneticVariation BEFREE The rs5443 polymorphism did not moderate depressive symptom trajectories, regardless of the measure used. 24882179

2014

dbSNP: rs5443
rs5443
CUI: C1696708
Disease: Prehypertension
Prehypertension
0.010 GeneticVariation BEFREE This study surveyed the frequencies of single nucleotide polymorphisms (SNPs) M235T AGT and C825T GNB3, and their association with insulin resistance, other biochemical markers and qualitative variables in subjects with high normal blood pressure and/or prehypertension in the Greek population. 24722130

2014

dbSNP: rs5443
rs5443
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.010 GeneticVariation BEFREE The pooled results of four studies fail to show associations of GNB3 C825T polymorphism with subtypes of IBS (constipation-dominant type, diarrhea-dominant type and mixed type). 24876757

2014

dbSNP: rs5443
rs5443
CUI: C0339510
Disease: Vitelliform Macular Dystrophy
Vitelliform Macular Dystrophy
0.010 GeneticVariation BEFREE The 3-locus MDR model comprising FTO rs8050136C/A and GNB3 rs1129649T/C and rs5443C/T emerged as the best disease conferring model. 23691120

2013

dbSNP: rs5443
rs5443
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE Using polymerase chain reaction and restriction fragment length polymorphism the allele frequency of the C825T polymorphism was investigated in 172 patients with prostate cancer. 22608746

2012

dbSNP: rs5443
rs5443
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 GeneticVariation BEFREE Using polymerase chain reaction and restriction fragment length polymorphism the allele frequency of the C825T polymorphism was investigated in 172 patients with prostate cancer. 22608746

2012

dbSNP: rs5443
rs5443
CUI: C0006145
Disease: Breast Diseases
Breast Diseases
0.010 GeneticVariation BEFREE To evaluate the prevalence of the C825T polymorphism in the GNB3 gene in women with and without breast cancer and its possible association with clinical or pathological features of breast disease. 22034052

2012

dbSNP: rs5443
rs5443
CUI: C2609247
Disease: Adrenal incidentaloma
Adrenal incidentaloma
0.010 GeneticVariation BEFREE Aim of the study was to assess the prevalence of C825T GNB3 gene polymorphism in patients with adrenal incidentaloma (AI) as well as its relation to the metabolic syndrome (MS) and cortisol status. 21979884

2011

dbSNP: rs5443
rs5443
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 GeneticVariation BEFREE Our aim in this study was to clarify any association of the GNB3 C825T polymorphism with gastric cancer risk in Japanese. 21198262

2010

dbSNP: rs5443
rs5443
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.010 GeneticVariation BEFREE The aim of the present observational study was to assess the value of the C825T polymorphism of the beta-3 subunit of G proteins (GNB3) as well as of variants in the SLC6A4 gene (5HTTLPR and STin2 VNTR) and DRD2 gene (TaqI A and NcoI) as predictive markers for consistency in headache response to triptans in migraine patients. 20488209

2010

dbSNP: rs5443
rs5443
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
0.010 GeneticVariation BEFREE The aim of the study was to examine the association between the G protein β3 subunit C825T polymorphism, associated with cardiovascular risk factors like hypertension (HT) and obesity and microalbuminuria (MA), reflecting the endothelial dysfunction in the atherosclerotic process. 20577224

2010

dbSNP: rs5443
rs5443
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 GeneticVariation BEFREE The Gly972Arg and C825T polymorphisms are associated neither with PCOS nor with metabolic syndrome in the Slovak female population. 20170352

2010

dbSNP: rs5443
rs5443
CUI: C3805278
Disease: Extrahepatic Cholangiocarcinoma
Extrahepatic Cholangiocarcinoma
0.010 GeneticVariation BEFREE Prognostic assessment of three single-nucleotide polymorphisms (GNB3 825C>T, BCL2-938C>A, MCL1-386C>G) in extrahepatic cholangiocarcinoma. 19968497

2010

dbSNP: rs5443
rs5443
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 GeneticVariation BEFREE Our aim in this study was to clarify any association of the GNB3 C825T polymorphism with gastric cancer risk in Japanese. 21198262

2010