rs4673, CYBA

N. diseases: 21
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.020 1.000 2 2004 2018
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
121 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2004 2004
Asthma
CUI: C0004096
Disease: Asthma
729 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2009 2009
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
131 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2004 2004
Cardiac fibrosis
CUI: C1397307
Disease: Cardiac fibrosis
4 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2013 2013
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
19 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2004 2004
Chronic granulomatous disease
CUI: C0018203
Disease: Chronic granulomatous disease
12 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2017 2017
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
29 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2012 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
189 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2018 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2014 2014
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
71 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2009 2009
Granulomatous Disease, Chronic, X-Linked
65 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2017 2017
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
63 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2004 2004
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
121 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2012 2012
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
20 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2014 2014
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2013 2013
Myocardial necrosis
CUI: C1442837
Disease: Myocardial necrosis
2 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2013 2013
Peroxisome Biogenesis Disorder, Complementation Group D
4 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2017 2017
Sleep Apnea, Obstructive
CUI: C0520679
Disease: Sleep Apnea, Obstructive
36 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2012 2012
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
16 0.679 0.429 16 88646828 missense variant A/G,T snp 0.70 0.67 0.010 1.000 1 2014 2014