Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
0.020 GeneticVariation phenotype BEFREE i) In the experimental mouse model, we observed that brain concentrations of cabergoline were tenfold higher in the mutant mice compared with their wild-type littermates, implying that cabergoline is indeed a substrate of the transporter P-gp at the blood-brain barrier level. ii) In the human study, we observed significant negative associations under cabergoline for the C-carriers and heterozygous CT individuals of SNP rs1045642 with two central side effects (frequency of fatigue and sleep disorders) and for the G-carriers of SNP rs2032582 with the enhancement of dizziness. 22672924 2012
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
0.020 GeneticVariation phenotype BEFREE CYP2D6 and ABCB1 polymorphisms were associated with the incidence of dizziness and prolonged corrected QT interval, respectively. 29061081 2017
Entrez Id: 1565
Gene Symbol: CYP2D6
CYP2D6
0.020 GeneticVariation phenotype BEFREE CYP2D6 and ABCB1 polymorphisms were associated with the incidence of dizziness and prolonged corrected QT interval, respectively. 29061081 2017
Entrez Id: 1565
Gene Symbol: CYP2D6
CYP2D6
0.020 GeneticVariation phenotype BEFREE Conventional dosage regimen led to toxic plasma concentration of NT and adverse effects such as dry mouth, constipation, and dizziness in this case with genotype CYP2D6*5/*10B. 15483356 2004
Entrez Id: 3553
Gene Symbol: IL1B
IL1B
0.010 GeneticVariation phenotype BEFREE Among the polymorphisms studied, only IL1β (-511C>T) was associated with dizziness, (p = 0.01), suggesting that IL1β may be related to hypotensive episodes and increased vascular permeability. 27228225 2018
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
0.010 GeneticVariation phenotype BEFREE Multiple SNPs in the putative promoter region of the CHRNB3 gene were nominally associated with "dizziness" experience from the first few cigarettes (P < 0.01). 19760673 2010
Entrez Id: 1139
Gene Symbol: CHRNA7
CHRNA7
0.010 GeneticVariation phenotype BEFREE The minor alleles of three SNPs in CHRNA6 (rs7812298, rs2304297, rs7828365) were associated with a decreased probability of dizziness (OR(95% CI)=0.54 (0.36, 0.81), 0.59 (0.40, 0.86) and 0.58 (0.36, 0.95), respectively), while one SNP in each of three other genes (rs3743077 (CHRNA3), rs755204 (CHRNA4), rs7178176 (CHRNA7)) was associated with an increased probability of dizziness (OR(95% CI)=1.40 (1.02, 1.90), 1.85 (1.05, 3.27) and 1.51 (1.06, 2.15), respectively). 24119711 2014
Entrez Id: 8973
Gene Symbol: CHRNA6
CHRNA6
0.010 GeneticVariation phenotype BEFREE The minor alleles of three SNPs in CHRNA6 (rs7812298, rs2304297, rs7828365) were associated with a decreased probability of dizziness (OR(95% CI)=0.54 (0.36, 0.81), 0.59 (0.40, 0.86) and 0.58 (0.36, 0.95), respectively), while one SNP in each of three other genes (rs3743077 (CHRNA3), rs755204 (CHRNA4), rs7178176 (CHRNA7)) was associated with an increased probability of dizziness (OR(95% CI)=1.40 (1.02, 1.90), 1.85 (1.05, 3.27) and 1.51 (1.06, 2.15), respectively). 24119711 2014
Entrez Id: 9211
Gene Symbol: LGI1
LGI1
0.010 GeneticVariation phenotype BEFREE Pain, peripheral manifestations, and stereotypic paroxysmal dizziness spells are common with LGI1-IgG. 28628235 2017
Entrez Id: 1136
Gene Symbol: CHRNA3
CHRNA3
0.010 GeneticVariation phenotype BEFREE The minor alleles of three SNPs in CHRNA6 (rs7812298, rs2304297, rs7828365) were associated with a decreased probability of dizziness (OR(95% CI)=0.54 (0.36, 0.81), 0.59 (0.40, 0.86) and 0.58 (0.36, 0.95), respectively), while one SNP in each of three other genes (rs3743077 (CHRNA3), rs755204 (CHRNA4), rs7178176 (CHRNA7)) was associated with an increased probability of dizziness (OR(95% CI)=1.40 (1.02, 1.90), 1.85 (1.05, 3.27) and 1.51 (1.06, 2.15), respectively). 24119711 2014
Entrez Id: 9311
Gene Symbol: ASIC3
ASIC3
0.010 GeneticVariation phenotype BEFREE However, whether the genetic variants of <i>ASIC3</i> are associated with people who suffer dizziness and balance impairment after mTBI remained unknown. 30804886 2019
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1
0.010 GeneticVariation phenotype BEFREE Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness. 25802247 2015
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
0.010 GeneticVariation phenotype BEFREE The aim of this meta-analysis is to identify the predictive strength in the current literature of OPRM1-A118G polymorphism to postoperative anesthetic reactions, including nausea, vomiting, pruritus and dizziness. 30323865 2018
Entrez Id: 1834
Gene Symbol: DSPP
DSPP
0.010 GeneticVariation phenotype BEFREE Of the incretin-based therapies, DPP-4Is had a lower risk of dizziness than GLP-1 RAs (OR: 0.76, 95% CI: 0.67 to 0.87; high quality). 31788342 2019
Entrez Id: 4311
Gene Symbol: MME
MME
0.010 GeneticVariation phenotype BEFREE The incidence of hypotension (OR 1.44; 95% CI 1.15-1.80; P < 0.05) and dizziness (OR 1.46; 95% CI 1.32-1.62; P < 0.05) was obviously increased in neprilysin-RAS inhibition compared with RAS inhibition. 31153654 2019
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.010 GeneticVariation phenotype BEFREE Conversely, LRRK2 G2019S carrier status significantly associated with reporting of milder daily symptoms of lightheadedness and several differences were observed at a false discovery rate < 0.1, including increased reporting of changes in walking as an initial symptom of disease, decreased reporting of lightheadedness upon standing, and milder symptoms related to daily functioning. 30154511 2018
Entrez Id: 348
Gene Symbol: APOE
APOE
0.010 GeneticVariation phenotype BEFREE Moreover, Symptoms like asthma (25%), cough (76.67%), dizziness (36.67%), eye irritation (88.33%), and shortness of breath (43.33%) were highly prevalent among biomass users than in LPG users. 29940511 2018
Entrez Id: 1312
Gene Symbol: COMT
COMT
0.010 GeneticVariation phenotype BEFREE In the ED in the hours after MVC, individuals with a COMT pain vulnerable genotype were more likely to report moderate-to-severe musculoskeletal neck pain (76 versus 41%, RR = 2.11 (1.33-3.37)), moderate or severe headache (61 versus 33%, RR = 3.15 (1.05-9.42)), and moderate or severe dizziness (26 versus 12%, RR = 1.97 (1.19-3.21)). 20688576 2011
Entrez Id: 1137
Gene Symbol: CHRNA4
CHRNA4
0.010 GeneticVariation phenotype BEFREE The minor alleles of three SNPs in CHRNA6 (rs7812298, rs2304297, rs7828365) were associated with a decreased probability of dizziness (OR(95% CI)=0.54 (0.36, 0.81), 0.59 (0.40, 0.86) and 0.58 (0.36, 0.95), respectively), while one SNP in each of three other genes (rs3743077 (CHRNA3), rs755204 (CHRNA4), rs7178176 (CHRNA7)) was associated with an increased probability of dizziness (OR(95% CI)=1.40 (1.02, 1.90), 1.85 (1.05, 3.27) and 1.51 (1.06, 2.15), respectively). 24119711 2014
Entrez Id: 5047
Gene Symbol: PAEP
PAEP
0.010 Biomarker phenotype BEFREE Pruritus, headache, nausea, rash, and dizziness were higher with TVR plus PEG-IFN-α2a-ribavirin during the first 12 weeks. 23685940 2013
Entrez Id: 2740
Gene Symbol: GLP1R
GLP1R
0.010 Biomarker phenotype BEFREE Ranking probability analysis indicated that GLP-1 RAs may have the greatest risk of both dizziness and headache among the nine treatments (22.5% and 23.4%, respectively), whereas DPP-4Is were in the middle (46.2% and 45.0%, respectively). 31788342 2019
Entrez Id: 3439
Gene Symbol: IFNA1
IFNA1
0.010 Biomarker phenotype BEFREE Pruritus, headache, nausea, rash, and dizziness were higher with TVR plus PEG-IFN-α2a-ribavirin during the first 12 weeks. 23685940 2013
Entrez Id: 79813
Gene Symbol: EHMT1
EHMT1
0.010 Biomarker phenotype BEFREE Ranking probability analysis indicated that GLP-1 RAs may have the greatest risk of both dizziness and headache among the nine treatments (22.5% and 23.4%, respectively), whereas DPP-4Is were in the middle (46.2% and 45.0%, respectively). 31788342 2019
Entrez Id: 64374
Gene Symbol: SIL1
SIL1
0.010 Biomarker phenotype BEFREE To study PNS vulnerability in MSS, intramuscular nerves fibres from MSS patients and from SIL1-deficient mice (woozy) as well as sciatic nerves and neuromuscular junctions (NMJ) from these mice have been investigated via transmission electron microscopic and immunofluorescence studies accompanied by transcript studies and unbiased proteomic profiling. 30468864 2019
Entrez Id: 26136
Gene Symbol: TES
TES
0.010 Biomarker phenotype BEFREE Low dose compared to standard doseThere was evidence of fewer adverse effects, measured as lower TESS scores, in the low-dose group in the short term (2 RCTs, n = 266, MD -3.99, 95% CI -5.75 to -2.24); and in one study there was evidence that the incidence of lethargy (RR 0.77, 95% CI 0.60 to 0.97), hypersalivation (RR 0.70, 95% CI 0.57 to 0.84), dizziness (RR 0.56, 95% CI 0.39 to 0.81) and tachycardia (RR 0.57, 95% CI 0.45 to 0.71) was less at low dose compared to standard dose. 28613395 2017