rs1800470, TGFB1

N. diseases: 107
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.
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2012 2012
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2012 2012
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2010 2010
Adenomatous Polyps
CUI: C0206677
Disease: Adenomatous Polyps
20 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2004 2004
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1 2011 2011
Asthma
CUI: C0004096
Disease: Asthma
1536 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2007 2007
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2007 2007
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2015 2015
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2015 2015
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2015 2015
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2001 2001
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2012 2012
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2006 2006
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2009 2009
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2015 2015
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2005 2005
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2017 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2012 2012
Cystic Fibrosis
CUI: C0010674
Disease: Cystic Fibrosis
704 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2007 2007
Deficiency of butyryl-CoA dehydrogenase
47 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2016 2016
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
32 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2006 2006
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1 2001 2001
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2014 2014
Duodenal Ulcer
CUI: C0013295
Disease: Duodenal Ulcer
33 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2007 2007