rs1800470, TGFB1

N. diseases: 46
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.100 0.933 15 2004 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1365 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.100 0.933 15 2004 2014
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
408 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.020 1.000 2 2010 2010
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
91 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2012 2012
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
428 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2010 2010
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
33 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1 2011 2011
Benign neoplasm of breast
CUI: C0346156
Disease: Benign neoplasm of breast
1 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2011 2011
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
142 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2016 2016
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
165 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2016 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
197 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2012 2012
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
331 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2006 2006
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
103 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2016 2016
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
33 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2014 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2012 2012
Cystic Fibrosis
CUI: C0010674
Disease: Cystic Fibrosis
489 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2007 2007
Deficiency of butyryl-CoA dehydrogenase
36 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2016 2016
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
15 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2006 2006
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2016 2016
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
115 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2014 2014
Duodenal Ulcer
CUI: C0013295
Disease: Duodenal Ulcer
29 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2007 2007
Gastric ulcer
CUI: C0038358
Disease: Gastric ulcer
7 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2007 2007
Gingival Diseases
CUI: C0017563
Disease: Gingival Diseases
9 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2014 2014
Graft-vs-Host Disease
CUI: C0018133
Disease: Graft-vs-Host Disease
8 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2016 2016
Graves Disease
CUI: C0018213
Disease: Graves Disease
213 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2015 2015
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
44 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1 2016 2016