Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6422324
rs6422324
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs61361928
rs61361928
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0948089
Disease:
Acute Coronary Syndrome
T 0.700 GeneticVariation GWASCAT Effect of genetic variations on ticagrelor plasma levels and clinical outcomes. 25935875 2015
dbSNP: rs4356975
rs4356975
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0162701
Disease:
Polysomnography
A 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0009402
Disease:
Colorectal Carcinoma
0.020 GeneticVariation BEFREE This meta-analysis confirmed the association of UGT2B7 rs7439366 with colorectal cancer risk, which may be a potential promising biomarker for prediction of colorectal cancer risk. 31082503 2019
dbSNP: rs7441774
rs7441774
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.020 GeneticVariation BEFREE In addition, the rs7441774 was found to be associated with breast cancer risk and significantly reduced papillary thyroid cancer risk in rs3924194 was also observed. 31082503 2019
dbSNP: rs7441774
rs7441774
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0678222
Disease:
Breast Carcinoma
0.020 GeneticVariation BEFREE In addition, the rs7441774 was found to be associated with breast cancer risk and significantly reduced papillary thyroid cancer risk in rs3924194 was also observed. 31082503 2019
dbSNP: rs7435335
rs7435335
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0678222
Disease:
Breast Carcinoma
0.020 GeneticVariation BEFREE A total of 190 patients with breast cancer treated with NAC were enrolled to detect the rs7435335 SNP by sequenom. 30552707 2018
dbSNP: rs7435335
rs7435335
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.020 GeneticVariation BEFREE A total of 190 patients with breast cancer treated with NAC were enrolled to detect the rs7435335 SNP by sequenom. 30552707 2018
dbSNP: rs7435335
rs7435335
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0678222
Disease:
Breast Carcinoma
0.020 GeneticVariation BEFREE This retrospective study was performed to evaluate the association between the UGT2B7 tagSNPs (rs12233719, rs4356975, rs7435335 and rs7441774) and breast cancer in Chinese females. 29272031 2018
dbSNP: rs7435335
rs7435335
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.020 GeneticVariation BEFREE This retrospective study was performed to evaluate the association between the UGT2B7 tagSNPs (rs12233719, rs4356975, rs7435335 and rs7441774) and breast cancer in Chinese females. 29272031 2018
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0014544
Disease:
Epilepsy
0.020 GeneticVariation BEFREE Single nucleotide polymorphisms UGT1A4 142T > G, L48V (*3), UGT1A4 70C > A, P24T (*2) and UGT2B7 802C > T, H268Y (*2) were determined in 40 women (47 pregnancies) with epilepsy treated with LTG. 29395496 2018
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0030193
Disease:
Pain
0.020 GeneticVariation BEFREE Conclusions Fentanyl sensitivity for cold pressor-induced pain was associated with the rs7439366, rs4587017, and rs1002849 SNPs of the UGT2B7 gene. 28256933 2018
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0030193
Disease:
Pain
0.020 GeneticVariation BEFREE The impact of UGT2B7 C802T and CYP3A4*1G polymorphisms on pain relief in cancer patients receiving oxycontin. 29502154 2018
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE The impact of UGT2B7 C802T and CYP3A4*1G polymorphisms on pain relief in cancer patients receiving oxycontin. 29502154 2018
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0006826
Disease:
Malignant Neoplasms
0.020 GeneticVariation BEFREE The impact of UGT2B7 C802T and CYP3A4*1G polymorphisms on pain relief in cancer patients receiving oxycontin. 29502154 2018
dbSNP: rs7441774
rs7441774
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0678222
Disease:
Breast Carcinoma
0.020 GeneticVariation BEFREE The frequency of rs7441774 G allele in the breast cancer cases was statistically significantly higher than in the controls (0.412 vs 0.358, P = .006; odds ratio [OR] = 1.27, 95% CI = 1.08-1.48). 29272031 2018
dbSNP: rs7441774
rs7441774
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.020 GeneticVariation BEFREE The frequency of rs7441774 G allele in the breast cancer cases was statistically significantly higher than in the controls (0.412 vs 0.358, P = .006; odds ratio [OR] = 1.27, 95% CI = 1.08-1.48). 29272031 2018
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0014544
Disease:
Epilepsy
0.020 GeneticVariation BEFREE These results suggested that ABCB1 rs1045642 and UGT2B7 rs7439366 may affect OXC pharmacokinetics and therapeutic efficacy in Han Chinese patients with epilepsy. 28837897 2017
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0009402
Disease:
Colorectal Carcinoma
0.020 GeneticVariation BEFREE To determine whether a genetic polymorphism in the detoxification enzyme UDP-glucuronosyltransferase 2B7 (UGT2B7) predisposes to CRC, 411 Caucasian patients with sporadic CRC and 600 Caucasian controls recruited from the same geographic area were genotyped for the functional UGT2B7 H268Y polymorphism. 19408577 2009
dbSNP: rs386675647
rs386675647
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0699885
Disease:
Carcinoma of bladder
0.020 GeneticVariation BEFREE UDP-glucuronosyltransferase 2B7 C802T (His268Tyr) polymorphism in bladder cancer cases. 18569595 2008
dbSNP: rs386675647
rs386675647
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0005684
Disease:
Malignant neoplasm of urinary bladder
0.020 GeneticVariation BEFREE UDP-glucuronosyltransferase 2B7 C802T (His268Tyr) polymorphism in bladder cancer cases. 18569595 2008
dbSNP: rs386675647
rs386675647
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0005695
Disease:
Bladder Neoplasm
0.020 GeneticVariation BEFREE UDP-glucuronosyltransferase 2B7 C802T (His268Tyr) polymorphism in bladder cancer cases. 18569595 2008
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0005695
Disease:
Bladder Neoplasm
0.020 GeneticVariation BEFREE UDP-glucuronosyltransferase 2B7 C802T (His268Tyr) polymorphism in bladder cancer cases. 18569595 2008
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0005684
Disease:
Malignant neoplasm of urinary bladder
0.020 GeneticVariation BEFREE UDP-glucuronosyltransferase 2B7 C802T (His268Tyr) polymorphism in bladder cancer cases. 18569595 2008
dbSNP: rs7439366
rs7439366
Entrez Id: 7364
Gene Symbol: UGT2B7
UGT2B7
CUI: C0699885
Disease:
Carcinoma of bladder
0.020 GeneticVariation BEFREE UDP-glucuronosyltransferase 2B7 C802T (His268Tyr) polymorphism in bladder cancer cases. 18569595 2008