rs4673, CYBA

N. diseases: 32
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.
Macroalbuminuric diabetic nephropathy
CUI: C2919365
Disease: Macroalbuminuric diabetic nephropathy
2 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2017 2017
Myocardial necrosis
CUI: C1442837
Disease: Myocardial necrosis
2 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2013 2013
Cardiac fibrosis
CUI: C1397307
Disease: Cardiac fibrosis
3 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2013 2013
Peroxisome Biogenesis Disorder, Complementation Group D
CUI: C1863999
Disease: Peroxisome Biogenesis Disorder, Complementation Group D
4 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2017 2017
Diabetic peripheral neuropathy
CUI: C0740447
Disease: Diabetic peripheral neuropathy
16 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2018 2018
Chronic granulomatous disease
CUI: C0018203
Disease: Chronic granulomatous disease
23 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2017 2017
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2013 2013
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2013 2013
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2012 2012
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2003 2003
Low Tension Glaucoma
CUI: C0152136
Disease: Low Tension Glaucoma
56 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2012 2012
Granulomatous Disease, Chronic, X-Linked
CUI: C1844376
Disease: Granulomatous Disease, Chronic, X-Linked
75 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2017 2017
Sleep Apnea, Obstructive
CUI: C0520679
Disease: Sleep Apnea, Obstructive
105 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2012 2012
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2004 2004
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2009 2009
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2003 2003
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2003 2003
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2012 2012
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2017 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2013 2013
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2018 2018
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2017 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2014 2014
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 0.010 1.000 1 2017 2017