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.
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
CUI: C0342783
Disease: 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
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2000 2015
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
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2015 2020
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
End stage cardiac failure
CUI: C1868938
Disease: End stage cardiac failure
2 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2001 2001
Erythema Multiforme
CUI: C0014742
Disease: Erythema Multiforme
2 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2017 2017
Filarial Elephantiases
CUI: C0013884
Disease: Filarial Elephantiases
10 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2011 2011
Gastric ulcer
CUI: C0038358
Disease: Gastric ulcer
7 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2007 2007
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2019 2019
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2019 2019
Graft-vs-Host Disease
CUI: C0018133
Disease: Graft-vs-Host Disease
25 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2016 2016
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2014 2014
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2015 2015
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2003 2003
Hyperplastic Polyp
CUI: C0333983
Disease: Hyperplastic Polyp
22 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2004 2004
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2008 2008
Hypocalciuric hypercalcemia, familial, type 1
CUI: C0342637
Disease: Hypocalciuric hypercalcemia, familial, type 1
58 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2005 2005
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
63 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2018 2018
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2005 2005
Immune thrombocytopenic purpura
CUI: C0398650
Disease: Immune thrombocytopenic purpura
35 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1 2003 2003