Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1209809979
rs1209809979
Entrez Id: 10327
Gene Symbol: AKR1A1
AKR1A1
CUI: C0683342
Disease:
hazardous drinking
0.010 GeneticVariation BEFREE This study investigated the association of 4 nonsynonymous SNPs in ADH genes (Arg48His and Arg370Cys in ADH1B gene; Arg272Gln and Ile350Val in ADH1C gene) with HD in people living with HIV-1. 28833276 2017
dbSNP: rs1209809979
rs1209809979
Entrez Id: 10327
Gene Symbol: AKR1A1
AKR1A1
CUI: C0346647
Disease:
Malignant neoplasm of pancreas
0.010 GeneticVariation BEFREE The impact of alcohol and polymorphisms in aldehyde dehydrogenase 2 (ALDH2) Glu504Lys, alcohol dehydrogenase (ADH) 1B His48Arg, and ADH1C Arg272Gln on PC risk was examined with multivariate analysis adjusted for potential confounders to estimate odds ratios (ORs) and 95% confidence intervals (CIs). 19068087 2009
dbSNP: rs1209809979
rs1209809979
Entrez Id: 10327
Gene Symbol: AKR1A1
AKR1A1
CUI: C0235974
Disease:
Pancreatic carcinoma
0.010 GeneticVariation BEFREE The impact of alcohol and polymorphisms in aldehyde dehydrogenase 2 (ALDH2) Glu504Lys, alcohol dehydrogenase (ADH) 1B His48Arg, and ADH1C Arg272Gln on PC risk was examined with multivariate analysis adjusted for potential confounders to estimate odds ratios (ORs) and 95% confidence intervals (CIs). 19068087 2009
dbSNP: rs61733010
rs61733010
Entrez Id: 10327
Gene Symbol: AKR1A1
AKR1A1
CUI: C0079772
Disease:
T-Cell Lymphoma
0.010 GeneticVariation BEFREE In addition, individuals variant homozygous for the CYBA (Ex4 + 11C > T) SNP had a 1.6-fold (95% CI = 1.1-2.4, P = 0.019) increased risk of NHL that was particularly pronounced for T-cell lymphoma (OR = 3.5, 95% CI = 1.3-9.6, P = 0.013), but was also associated with non-significant increased risks for each of the common B-cell histologies. 17149600 2007
dbSNP: rs61733010
rs61733010
Entrez Id: 10327
Gene Symbol: AKR1A1
AKR1A1
CUI: C0024305
Disease:
Lymphoma, Non-Hodgkin
0.010 GeneticVariation BEFREE In addition, individuals variant homozygous for the CYBA (Ex4 + 11C > T) SNP had a 1.6-fold (95% CI = 1.1-2.4, P = 0.019) increased risk of NHL that was particularly pronounced for T-cell lymphoma (OR = 3.5, 95% CI = 1.3-9.6, P = 0.013), but was also associated with non-significant increased risks for each of the common B-cell histologies. 17149600 2007
dbSNP: rs753056697
rs753056697
Entrez Id: 10327
Gene Symbol: AKR1A1
AKR1A1
CUI: C0027868
Disease:
Neuromuscular Diseases
0.010 GeneticVariation BEFREE Structure and properties of K141E mutant of small heat shock protein HSP22 (HspB8, H11) that is expressed in human neuromuscular disorders. 16949546 2006
dbSNP: rs753056697
rs753056697
Entrez Id: 10327
Gene Symbol: AKR1A1
AKR1A1
CUI: C0235025
Disease:
Peripheral motor neuropathy
0.010 GeneticVariation BEFREE Some properties of the K141E mutant of human HSP22 that is expressed in distal hereditary motor neuropathy were investigated. 16949546 2006