CYBA, cytochrome b-245 alpha chain, 1535

N. diseases: 177; N. variants: 23
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7195830
rs7195830
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE The CYBA Gene (⁎)49A>G Polymorphism (rs7195830) Is Associated with Hypertension in Patients with Coronary Artery Disease. 27314008 2016
dbSNP: rs7195830
rs7195830
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE The CYBA Gene (⁎)49A>G Polymorphism (rs7195830) Is Associated with Hypertension in Patients with Coronary Artery Disease. 27314008 2016
dbSNP: rs7195830
rs7195830
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C0010068
Disease:
Coronary heart disease
0.010 GeneticVariation BEFREE The CYBA Gene (⁎)49A>G Polymorphism (rs7195830) Is Associated with Hypertension in Patients with Coronary Artery Disease. 27314008 2016
dbSNP: rs7195830
rs7195830
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE The CYBA Gene (⁎)49A>G Polymorphism (rs7195830) Is Associated with Hypertension in Patients with Coronary Artery Disease. 27314008 2016
dbSNP: rs1049255
rs1049255
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C2316810
Disease:
Chronic kidney disease stage 5
0.010 GeneticVariation BEFREE Our results suggested that rs1049255 polymorphism of CYBA modified the risk of ESRD (p  =  0.019; OR  =  0.625; 95%CI  =  0.424-0.921). 26627442 2016
dbSNP: rs1049255
rs1049255
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.010 GeneticVariation BEFREE Our results suggested that rs1049255 polymorphism of CYBA modified the risk of ESRD (p  =  0.019; OR  =  0.625; 95%CI  =  0.424-0.921). 26627442 2016
dbSNP: rs546127665
rs546127665
Entrez Id: 1535;4597
Gene Symbol: CYBA;MVD
CYBA;MVD
CUI: C3553549
Disease:
POROKERATOSIS 7, MULTIPLE TYPES
0.700 GeneticVariation UNIPROT Genomic variations of the mevalonate pathway in porokeratosis. 26202976 2015
dbSNP: rs9932581
rs9932581
Entrez Id: 1535;4597
Gene Symbol: CYBA;MVD
CYBA;MVD
CUI: C0022658
Disease:
Kidney Diseases
0.010 GeneticVariation BEFREE The major G-allele of rs9932581 was associated with the incidence of renal events defined as new cases of microalbuminuria or the progression to a more severe stage of nephropathy during follow-up (HR 1.59, 95% CI 1.17-2.18, P=0.003) in SURGENE. 25862415 2015
dbSNP: rs4673
rs4673
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.020 GeneticVariation BEFREE A number of epidemiological studies have explored the association between NAD(P)H oxidase P22 phox gene C242T (rs4673) polymorphism and susceptibility to type 2 diabetes mellitus (T2DM), but the results are still debatable. 24156725 2014
dbSNP: rs7195830
rs7195830
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1561643
Disease:
Chronic Kidney Diseases
0.010 GeneticVariation BEFREE The AA genotype of rs7195830 is independently associated with lower estimated glomerular filtration rate and is significantly associated with CKD. 24033955 2013
dbSNP: rs104894510
rs104894510
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1856255
Disease:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
0.800 GeneticVariation UNIPROT Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. 23910690 2013
dbSNP: rs104894513
rs104894513
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1856255
Disease:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
0.800 GeneticVariation UNIPROT Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. 23910690 2013
dbSNP: rs104894514
rs104894514
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1856255
Disease:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
0.800 GeneticVariation UNIPROT Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. 23910690 2013
dbSNP: rs104894515
rs104894515
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1856255
Disease:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
0.800 GeneticVariation UNIPROT Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. 23910690 2013
dbSNP: rs179363892
rs179363892
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1856255
Disease:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
0.800 GeneticVariation UNIPROT Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. 23910690 2013
dbSNP: rs28941476
rs28941476
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1856255
Disease:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
0.800 GeneticVariation UNIPROT Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. 23910690 2013
dbSNP: rs179363890
rs179363890
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1856255
Disease:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
0.700 GeneticVariation UNIPROT Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. 23910690 2013
dbSNP: rs179363891
rs179363891
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1856255
Disease:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
0.700 GeneticVariation UNIPROT Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. 23910690 2013
dbSNP: rs179363893
rs179363893
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1856255
Disease:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
0.700 GeneticVariation UNIPROT Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. 23910690 2013
dbSNP: rs179363894
rs179363894
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1856255
Disease:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
0.700 GeneticVariation UNIPROT Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. 23910690 2013
dbSNP: rs4673
rs4673
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.020 GeneticVariation BEFREE According to the results of cross-sectional study, the tested polymorphism of the NADPH oxidase P22phox gene (rs4673) was found to be associated with the development of AH, indicating that the oxidative stress gene NADPH oxidase might be implicated in the pathogenesis of AH in subjects with type 2 diabetes. 23701472 2014
dbSNP: rs4673
rs4673
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE According to the results of cross-sectional study, the tested polymorphism of the NADPH oxidase P22phox gene (rs4673) was found to be associated with the development of AH, indicating that the oxidative stress gene NADPH oxidase might be implicated in the pathogenesis of AH in subjects with type 2 diabetes. 23701472 2014
dbSNP: rs4673
rs4673
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE Using a retrospective case-control design, we evaluated cardiac histological lesions and NADPH genotype (polymorphisms rs1883112, rs4673, and rs13058338) in 97 consecutive decedents with a cancer diagnosis (48 treated with anthracyclines). 23576480 2013
dbSNP: rs4673
rs4673
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1397307
Disease:
Cardiac fibrosis
0.010 GeneticVariation BEFREE In patients receiving anthracyclines, NADPH oxidase polymorphism rs4673 protected against focal myocardial necrosis (odds ratio [OR], 0.11; 95% confidence interval [CI], 0.20-0.63) whereas rs1883112 was strongly associated with cardiac fibrosis (OR, 5.11; 95% CI, 1.59-16.43), which was present in all homozygotes. 23576480 2013
dbSNP: rs4673
rs4673
Entrez Id: 1535
Gene Symbol: CYBA
CYBA
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE Using a retrospective case-control design, we evaluated cardiac histological lesions and NADPH genotype (polymorphisms rs1883112, rs4673, and rs13058338) in 97 consecutive decedents with a cancer diagnosis (48 treated with anthracyclines). 23576480 2013