|
rs151344517
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias.
|
20725928 |
2010 |
|
rs796053124
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.
|
20956790 |
2010 |
|
rs1163944538
|
|
GA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs121908216
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs121912683
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs1352010373
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs144948296
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1555735545
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs28937900
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs397507478
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs61755320
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs797045032
|
|
TC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1799971
|
|
|
0.020 |
GeneticVariation |
BEFREE |
OPRM1-A118G polymorphism (A > G) is associated with a reduced risk of postoperative vomiting, but not nausea, pruritus and dizziness.
|
30323865 |
2018 |
|
rs1799971
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Additionally, the combined genotype of CYP3A4*18B and OPRM1 A118G may affect fentanyl doses administered for pain control, but not postoperative nausea, vomiting and dizziness.
|
23313934 |
2013 |
|
rs7136446
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Patients carrying minor alleles of rs7136446 and rs972936 showed more dizziness and multiple neuropsychiatric symptoms after brain injury.
|
31787098 |
2019 |
|
rs77485247
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We selected one SNP, rs77485247 in HRH4 and conducted an exploratory investigation of its correlations with the symptoms of vertigo and proinflammatory cytokines levels in MD patients.
|
31133025 |
2019 |
|
rs972936
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Patients carrying minor alleles of rs7136446 and rs972936 showed more dizziness and multiple neuropsychiatric symptoms after brain injury.
|
31787098 |
2019 |
|
rs1048101
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Furthermore, the SNPs within ADRA1A [rs10</span>48101 (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 |
|
rs16148
|
|
|
0.010 |
GeneticVariation |
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 |
|
rs16476
|
|
|
0.010 |
GeneticVariation |
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 |
|
rs1783901
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our results suggest that the SNPs rs1939012 and rs1783901 may play a potential role of gene regulation and/or epistasis in a complex etiology of vertigo.
|
30300896 |
2018 |
|
rs1939012
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our results suggest that the SNPs rs1939012 and rs1783901 may play a potential role of gene regulation and/or epistasis in a complex etiology of vertigo.
|
30300896 |
2018 |
|
rs2053044
|
|
|
0.010 |
GeneticVariation |
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 |
|
rs28365031
|
|
|
0.010 |
GeneticVariation |
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 |
|
rs3802241
|
|
|
0.010 |
GeneticVariation |
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 |