Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1002424
rs1002424
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASDB Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. 22037555 2011
dbSNP: rs10074991
rs10074991
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASDB Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. 22037555 2011
dbSNP: rs13361707
rs13361707
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASDB Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. 22037555 2011
dbSNP: rs928784854
rs928784854
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.700 GeneticVariation UNIPROT
dbSNP: rs10074991
rs10074991
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.020 GeneticVariation BEFREE Haplotype analysis indicated A-G-C-T-C-G haplotype (rs6882903, rs10074991, rs13361707, rs3805490, rs154268 and rs461404) is associated with increased risk of g</span>astric cancer (OR = 1.29, 95%CI: 1.02-1.62, p = 0.035). 30253744 2018
dbSNP: rs13361707
rs13361707
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0006826
Disease:
Malignant Neoplasms
0.020 GeneticVariation BEFREE To sum up, PRKAA1 rs13361707 polymorphism is not participant with the increased risk of cancer, while the A allele of PRKAA1 rs10074991 revealed a significant decrease risk. 30340465 2018
dbSNP: rs13361707
rs13361707
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE To sum up, PRKAA1 rs13361707 polymorphism is not participant with the increased risk of cancer, while the A allele of PRKAA1 rs10074991 revealed a significant decrease risk. 30340465 2018
dbSNP: rs154268
rs154268
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.020 GeneticVariation BEFREE Furthermore, the rs154268 and rs461404 were also found associated with increased gastric cancer risk, which may be influenced by age, tumor type and differentiation, and tumor stage. 30253744 2018
dbSNP: rs154268
rs154268
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0699791
Disease:
Stomach Carcinoma
0.020 GeneticVariation BEFREE Furthermore, the rs154268 and rs461404 were also found associated with increased gastric cancer risk, which may be influenced by age, tumor type and differentiation, and tumor stage. 30253744 2018
dbSNP: rs6882903
rs6882903
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0699791
Disease:
Stomach Carcinoma
0.020 GeneticVariation BEFREE Haplotype analysis indicated A-G-C-T-C-G haplotype (rs6882903, rs10074991, rs13361707, rs3805490, rs154268 and rs461404) is associated with increased risk of gastric cancer (OR = 1.29, 95%CI: 1.02-1.62, p = 0.035). 30253744 2018
dbSNP: rs6882903
rs6882903
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.020 GeneticVariation BEFREE Haplotype analysis indicated A-G-C-T-C-G haplotype (rs6882903, rs10074991, rs13361707, rs3805490, rs154268 and rs461404) is associated with increased risk of gastric cancer (OR = 1.29, 95%CI: 1.02-1.62, p = 0.035). 30253744 2018
dbSNP: rs13361707
rs13361707
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0006826
Disease:
Malignant Neoplasms
0.020 GeneticVariation BEFREE Also those with a hereditary background including the risk alleles PLCE1 rs2274223 and PTGER4/PRKAA1 rs13361707 were 3 times more susceptible to cardia cancer than those without. 27127881 2016
dbSNP: rs13361707
rs13361707
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE Also those with a hereditary background including the risk alleles PLCE1 rs2274223 and PTGER4/PRKAA1 rs13361707 were 3 times more susceptible to cardia cancer than those without. 27127881 2016
dbSNP: rs10074991
rs10074991
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.020 GeneticVariation BEFREE Most notably, subjects with a homozygous minor allele in SNP rs10074991 showed 2.15 times the risk of gastric cancer</span> as subjects without a minor allele. 25024613 2014
dbSNP: rs154268
rs154268
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0699791
Disease:
Stomach Carcinoma
0.020 GeneticVariation BEFREE In the recessive model, SNPs rs154268 (OR = 1.66, 95%CI: 1.22-2.26), rs3805486 (OR = 0.63, 95%CI: 0.46-0.85), and rs10074991 (OR = 1.47, 95%CI: 1.15-1.88) were significant risk or protective factors for gastric cancer. 25024613 2014
dbSNP: rs154268
rs154268
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.020 GeneticVariation BEFREE In the recessive model, SNPs rs154268 (OR = 1.66, 95%CI: 1.22-2.26), rs3805486 (OR = 0.63, 95%CI: 0.46-0.85), and rs10074991 (OR = 1.47, 95%CI: 1.15-1.88) were significant risk or protective factors for gastric cancer. 25024613 2014
dbSNP: rs6882903
rs6882903
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.020 GeneticVariation BEFREE In the dominant model, SNPs rs13361707 [odds ratio (OR) = 1.51, 95%CI: 1.07-2.11)], rs154268 (OR = 1.65, 95%CI: 1.22-2.22), rs6882903 (OR = 1.48, 95%CI: 1.09-2.00), and rs10074991 (OR = 1.53, 95%CI: 1.09-2.16) were significantly associated with an increased risk of gastric cancer. 25024613 2014
dbSNP: rs6882903
rs6882903
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0699791
Disease:
Stomach Carcinoma
0.020 GeneticVariation BEFREE In the dominant model, SNPs rs13361707 [odds ratio (OR) = 1.51, 95%CI: 1.07-2.11)], rs154268 (OR = 1.65, 95%CI: 1.22-2.22), rs6882903 (OR = 1.48, 95%CI: 1.09-2.00), and rs10074991 (OR = 1.53, 95%CI: 1.09-2.16) were significantly associated with an increased risk of gastric cancer. 25024613 2014
dbSNP: rs10074991
rs10074991
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE Our meta-analysis showed that AMPK pathway had significant associations with progression-free survival (PFS; p < 0.001) and overall survival (OS; p < 0.001), but not with tumor response (TR; p = 0.220): PRKAA1 rs13361707 was significantly associated with favorable PFS (log HR = -0.219, SE = 0.073, p = 0.003), as well as PRKAA1 rs10074991 (log HR = -0.215, SE = 0.073, p = 0.003), and there were suggestive associations of PRKAG1 rs1138908 with unfavorable OS (log HR = 0.170, SE = 0.083, p = 0.041), and of UBE2O rs3803739 with unfavorable PFS (log HR = 0.137, SE = 0.068, p = 0.042) and OS (log HR = 0.210, SE = 0.077, p = 0.006), although these results were not significant after false discovery rate adjustment. 30856283 2019
dbSNP: rs13361707
rs13361707
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE Our meta-analysis showed that AMPK pathway had significant associations with progression-free survival (PFS; p < 0.001) and overall survival (OS; p < 0.001), but not with tumor response (TR; p = 0.220): PRKAA1 rs13361707 was significantly associated with favorable PFS (log HR = -0.219, SE = 0.073, p = 0.003), as well as PRKAA1 rs10074991 (log HR = -0.215, SE = 0.073, p = 0.003), and there were suggestive associations of PRKAG1 rs1138908 with unfavorable OS (log HR = 0.170, SE = 0.083, p = 0.041), and of UBE2O rs3803739 with unfavorable PFS (log HR = 0.137, SE = 0.068, p = 0.042) and OS (log HR = 0.210, SE = 0.077, p = 0.006), although these results were not significant after false discovery rate adjustment. 30856283 2019
dbSNP: rs10074991
rs10074991
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE To sum up, PRKAA1 rs13361707 polymorphism is not participant with the increased risk of cancer, while the A allele of PRKAA1 rs10074991 revealed a significant decrease risk. 30340465 2018
dbSNP: rs10074991
rs10074991
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE To sum up, PRKAA1 rs13361707 polymorphism is not participant with the increased risk of cancer, while the A allele of PRKAA1 rs10074991 revealed a significant decrease risk. 30340465 2018
dbSNP: rs154268
rs154268
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE Furthermore, the rs154268 and rs461404 were also found associated with increased gastric cancer risk, which may be influenced by age, tumor type and differentiation, and tumor stage. 30253744 2018
dbSNP: rs3805490
rs3805490
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.010 GeneticVariation BEFREE Haplotype analysis indicated A-G-C-T-C-G haplotype (rs6882903, rs10074991, rs13361707, rs3805490, rs154268 and rs461404) is associated with increased risk of gastric cancer (OR = 1.29, 95%CI: 1.02-1.62, p = 0.035). 30253744 2018
dbSNP: rs3805490
rs3805490
Entrez Id: 5562
Gene Symbol: PRKAA1
PRKAA1
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE Haplotype analysis indicated A-G-C-T-C-G haplotype (rs6882903, rs10074991, rs13361707, rs3805490, rs154268 and rs461404) is associated with increased risk of gastric cancer (OR = 1.29, 95%CI: 1.02-1.62, p = 0.035). 30253744 2018