Source: ALL
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 CYP2D6 and ABCB1 polymorphisms were associated with the incidence of dizziness and prolonged corrected QT interval, respectively. 29061081 2017
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: 43
Gene Symbol: ACHE
ACHE
0.010 AlteredExpression phenotype BEFREE Abnormal serum AChE levels associated with pesticide exposure are associated with AChE levels and symptoms such as coughing, being tired, dizziness, and dry skin and irritation. 30047860 2018
Entrez Id: 49
Gene Symbol: ACR
ACR
0.010 Biomarker phenotype BEFREE ACR Appropriateness Criteria<sup>®</sup> Hearing Loss and/or Vertigo. 30392601 2018
Entrez Id: 51816
Gene Symbol: ADA2
ADA2
0.100 Biomarker phenotype HPO
Entrez Id: 111
Gene Symbol: ADCY5
ADCY5
0.010 Biomarker phenotype BEFREE Sixty-eight patients with AC/V-P shunts had a higher incidence of head trauma (P = 0.014), younger age at onset (P < 0.001), and lower incidence of dizziness (P = 0.013) than did those without AC/V-P shunts. 30797913 2019
Entrez Id: 148
Gene Symbol: ADRA1A
ADRA1A
0.010 GeneticVariation phenotype BEFREE Furthermore, the SNPs within ADRA1A [rs1048101 (T>C)], NPY [rs16476 (A>C), rs16148 (T>C)], as well as ADRB1 [rs28365031 (A>G)] all appeared to predict the prognosis of cervical vertigo in a relatively accurate way (all P < .05). 29197114 2018
Entrez Id: 153
Gene Symbol: ADRB1
ADRB1
0.010 GeneticVariation phenotype BEFREE Furthermore, the SNPs within ADRA1A [rs1048101 (T>C)], NPY [rs16476 (A>C), rs16148 (T>C)], as well as ADRB1 [rs28365031 (A>G)] all appeared to predict the prognosis of cervical vertigo in a relatively accurate way (all P < .05). 29197114 2018
Entrez Id: 154
Gene Symbol: ADRB2
ADRB2
0.010 GeneticVariation phenotype BEFREE Finally, the severity of cervical vertigo was classified according to the JOA scoring, and the recovery rate (RR) of cervical vertigo was calculated in light of the formula as: [Formula: see text] RESULTS: The SNPs within ADRA1A [rs1048101 (T>C) and rs3802241 (C>T)], NPY [rs16476 (A>C), rs16148 (T>C), and rs5574 (C>T)], ADRB1 [rs28365031 (A>G)] and ADRB2 [rs2053044 (A>G)] were all significantly associated with regulated risk of cervical vertigo (all P < .05). 29197114 2018
Entrez Id: 10939
Gene Symbol: AFG3L2
AFG3L2
0.100 CausalMutation phenotype CLINVAR Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias. 20725928 2010
Entrez Id: 9049
Gene Symbol: AIP
AIP
0.100 Biomarker phenotype HPO
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: 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: 477
Gene Symbol: ATP1A2
ATP1A2
0.100 Biomarker phenotype HPO
Entrez Id: 551
Gene Symbol: AVP
AVP
0.010 Biomarker phenotype BEFREE We evaluated whether copeptin and S100b protein (PS100b) assessment, alone or in combination, could rule out stroke in patients visiting EDs for dizziness. 31387626 2019
Entrez Id: 567
Gene Symbol: B2M
B2M
0.100 Biomarker phenotype HPO
Entrez Id: 54880
Gene Symbol: BCOR
BCOR
0.100 Biomarker phenotype HPO
Entrez Id: 673
Gene Symbol: BRAF
BRAF
0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 673
Gene Symbol: BRAF
BRAF
0.100 Biomarker phenotype HPO
Entrez Id: 720
Gene Symbol: C4A
C4A
0.100 Biomarker phenotype HPO
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A
0.130 Biomarker phenotype HPO
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A
0.130 GeneticVariation phenotype BEFREE The present authors studied a 55-year-old-patient homozygous for the SCA6 gene who experienced frequent attacks of positional vertigo at 37 years of age with subsequent staggering gait and night blindness. 12081723 2002
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A
0.130 GeneticVariation phenotype CLINVAR
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A
0.130 GeneticVariation phenotype BEFREE Mutations in CACNA1A are not common in families with migraine headaches and episodic vertigo. 9741473 1998
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A
0.130 GeneticVariation phenotype BEFREE Episodic ataxia type 2 is a prototypical episodic vertigo and ataxia syndrome that is caused by mutations in the calcium channel gene CACNA1A. 11796946 2002