ADORA2A, adenosine A2a receptor, 135

N. diseases: 213; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2298383
rs2298383
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0349217
Disease:
Depressive episode, unspecified
0.010 GeneticVariation BEFREE Here, we examined an association between a single nucleotide polymorphism in A<sub>2A</sub> receptor gene (ADORA2A, rs2298383 SNP) with current depressive episode and symptom profile. 30511252 2019
dbSNP: rs2298383
rs2298383
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0011570
Disease:
Mental Depression
0.010 GeneticVariation BEFREE Our data support an important role for ADORA2A rs2298383 SNP in clinical heterogeneity associated with depression. 30511252 2019
dbSNP: rs2298383
rs2298383
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.010 GeneticVariation BEFREE The combination of MTHFR 1298AA along with ADORA2A rs2298383 CC or CT genotypes occurring in one-third of RA patients showed a higher frequency of general nodules 15/59 (25.4%) as well as developing nodules during MTX treatment 13/59 (22.0%) in comparison with the overall studied group: 24/185 (13.0%) and 19/185 (10.3%), respectively. 27846189 2017
dbSNP: rs2298383
rs2298383
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0270612
Disease:
Leukoencephalopathy
0.010 GeneticVariation BEFREE ADORA2A rs2298383 and high cumulative dose of systemic MTX administration were significantly associated with MTX-related leukoencephalopathy. 27399166 2016
dbSNP: rs2298383
rs2298383
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0392156
Disease:
Akathisia
0.010 GeneticVariation BEFREE We found an association between ADORA1 rs3766566 and psychopathological symptoms (p = 0.006), in particular, with positive psychopathological symptoms (p = 0.010) and general psychopathological symptoms (p = 0.023), between ADORA2A rs2298383 and general psychopathological symptoms (p = 0.046), and between ADORA2A rs5751876 and akathisia (p = 0.015). 27195966 2016
dbSNP: rs5751876
rs5751876
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C1836438
Disease:
Familial neurocardiogenic syncope
0.010 GeneticVariation BEFREE Adenosine A(2A) receptor 1083 T > C polymorphism is not associated with the positivity of HUT and its proposed role in predisposition to VVS was not confirmed. 26710963 2016
dbSNP: rs5751876
rs5751876
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0392156
Disease:
Akathisia
0.010 GeneticVariation BEFREE We found an association between ADORA1 rs3766566 and psychopathological symptoms (p = 0.006), in particular, with positive psychopathological symptoms (p = 0.010) and general psychopathological symptoms (p = 0.023), between ADORA2A rs2298383 and general psychopathological symptoms (p = 0.046), and between ADORA2A rs5751876 and akathisia (p = 0.015). 27195966 2016
dbSNP: rs5751876
rs5751876
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0039070
Disease:
Syncope
0.010 GeneticVariation BEFREE One thousand and eighty-three T > C single nucleotide polymorphism in the adenosine A(2A) receptor gene (rs5751876) was evaluated in 347 patients with syncope and in 85 subjects without history of syncope (54 men, mean age 41.7 ± 16.3). 26710963 2016
dbSNP: rs4822489
rs4822489
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0018802
Disease:
Congestive heart failure
0.010 GeneticVariation BEFREE The findings of this study suggest that rs4822489 may contribute to the severity of CHF in the northern Chinese. 25629231 2015
dbSNP: rs5751876
rs5751876
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0040517
Disease:
Gilles de la Tourette syndrome
0.010 GeneticVariation BEFREE The minor allele T frequency of rs5751876 was lower in GTS patients with </span>co-morbid attention deficit hyperactivity disorder (p = 0.022), and TT+TC genotypes were less frequent in the non-OCD anxiety disorder group (p = 0.045). 26317759 2015
dbSNP: rs5751876
rs5751876
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0024530
Disease:
Malaria
0.010 GeneticVariation BEFREE Single-locus analysis showed significant association of 2 SNPs; rs5751876 (OR=3.2(2.0-5.2); p=0.0006) of ADORA2A and rs2230345 (OR=0.3(0.2-0.5); p=0.0006) of GRK5 with malaria. 26066465 2015
dbSNP: rs5751876
rs5751876
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.010 GeneticVariation BEFREE The minor allele T frequency of rs5751876 was lower in GTS patients with co-morbid attention deficit hyperactivity disorder (p = 0.022), and TT+TC genotypes were less frequent in the non-OCD anxiety disorder group (p = 0.045). 26317759 2015
dbSNP: rs9624472
rs9624472
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0024530
Disease:
Malaria
0.010 GeneticVariation BEFREE The mean of the serum creatinine levels were significantly higher in patients with variant GG (p=0.006) of rs9624472 in ADORA2A gene compared to AA and AG genotypes in complicated Pf malaria cases, with the G allele also showing increased risk for malaria (OR=1.3(1.1-1.6); p=0.017). 26066465 2015
dbSNP: rs35320474
rs35320474
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0003578
Disease:
Apnea
0.010 GeneticVariation BEFREE Logistic regression analysis showed a significant correlation between rs35320474-C/T and T/T genotypes and apnoea and BPD development. 22462821 2012
dbSNP: rs35320474
rs35320474
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0006287
Disease:
Bronchopulmonary Dysplasia
0.010 GeneticVariation BEFREE Logistic regression analysis showed a significant correlation between rs35320474-C/T and T/T genotypes and apnoea and BPD development. 22462821 2012
dbSNP: rs2236624
rs2236624
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C1845050
Disease:
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
0.010 GeneticVariation BEFREE A significant association was observed between SNP rs2236624 and PDR in the recessive genetic model. 21088442 2011
dbSNP: rs4822489
rs4822489
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C1845050
Disease:
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
0.010 GeneticVariation BEFREE Similarly, for SNP rs4822489, an association between PDR and T allele homozygosity was observed following covariate adjustment (OR = 0.55; 95% CI: 0.31-0.92; p = 0.04). 21088442 2011
dbSNP: rs5751876
rs5751876
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0271183
Disease:
Severe myopia
0.010 GeneticVariation BEFREE The reduced frequency of the heterozygote rs5751876 genotype in subjects suggests a possible association of A(2A)R with high myopia in a Chinese population. 22740769 2011
dbSNP: rs5996696
rs5996696
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE Two ADORA2A polymorphisms were inversely associated with PD risk - rs71651683, a 5' variant (adjusted allelic OR = 0.51, 95% CI 0.33-0.80, permutation-adjusted P = 0.015) and rs5996696, a promoter region variant (adjusted OR for AC and CC genotypes compared with the AA wild-type genotype were 0.76 (95% CI 0.57-1.02) and 0.37 (95% CI 0.13-1.01), respectively (permutation-adjusted P for trend = 0.04). 21281405 2011
dbSNP: rs71651683
rs71651683
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE Two ADORA2A polymorphisms were inversely associated with PD risk - rs71651683, a 5' variant (adjusted allelic OR = 0.51, 95% CI 0.33-0.80, permutation-adjusted P = 0.015) and rs5996696, a promoter region variant (adjusted OR for AC and CC genotypes compared with the AA wild-type genotype were 0.76 (95% CI 0.57-1.02) and 0.37 (95% CI 0.13-1.01), respectively (permutation-adjusted P for trend = 0.04). 21281405 2011
dbSNP: rs2236624
rs2236624
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.010 GeneticVariation BEFREE Nominal association with the disorder was observed for rs2236624-CC, and phenotypic variability in ASD symptoms was influenced by rs3761422, rs5751876 and rs35320474. 19565319 2010
dbSNP: rs3761422
rs3761422
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0236734
Disease:
Caffeine related disorders
0.010 GeneticVariation BEFREE Apart from the almost completely linked ADORA2A SNP rs3761422, no other of eight ADORA2A and seven ADORA1 SNPs studied were found to be clearly associated with effects of caffeine on anxiety, alertness, or headache. 20520601 2010
dbSNP: rs3761422
rs3761422
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0003467
Disease:
Anxiety
0.010 GeneticVariation BEFREE Apart from the almost completely linked ADORA2A SNP rs3761422, no other of eight ADORA2A and seven ADORA1 SNPs studied were found to be clearly associated with effects of caffeine on anxiety, alertness, or headache. 20520601 2010
dbSNP: rs3761422
rs3761422
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0018681
Disease:
Headache
0.010 GeneticVariation BEFREE Apart from the almost completely linked ADORA2A SNP rs3761422, no other of eight ADORA2A and seven ADORA1 SNPs studied were found to be clearly associated with effects of caffeine on anxiety, alertness, or headache. 20520601 2010
dbSNP: rs3761422
rs3761422
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0003469
Disease:
Anxiety Disorders
0.010 GeneticVariation BEFREE Apart from the almost completely linked ADORA2A SNP rs3761422, no other of eight ADORA2A and seven ADORA1 SNPs studied were found to be clearly associated with effects of caffeine on anxiety, alertness, or headache. 20520601 2010