rs1982073, TGFB1

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.
Bone Diseases
CUI: C0005940
Disease: Bone Diseases
10 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2016 2016
Vesicoureteral Reflux 1
CUI: C4551858
Disease: Vesicoureteral Reflux 1
10 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2008 2008
Pneumonitis
CUI: C3714636
Disease: Pneumonitis
13 0.649 0.640 19 41353016 missense variant G/A;C snv 0.020 1.000 2 2009 2016
Vesico-Ureteral Reflux
CUI: C0042580
Disease: Vesico-Ureteral Reflux
23 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2008 2008
Rheumatic Heart Disease
CUI: C0035439
Disease: Rheumatic Heart Disease
33 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2016 2016
Squamous cell carcinoma of oropharynx
CUI: C0280313
Disease: Squamous cell carcinoma of oropharynx
33 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2018 2018
Osteoporotic Fractures
CUI: C0521170
Disease: Osteoporotic Fractures
40 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2016 2016
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2019 2019
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2019 2019
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2019 2019
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2013 2013
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2017 2017
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2013 2013
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2019 2019
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2019 2019
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2019 2019
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2010 2010
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2006 2006
Cystic Fibrosis
CUI: C0010674
Disease: Cystic Fibrosis
704 0.649 0.640 19 41353016 missense variant G/A;C snv 0.020 1.000 2 2007 2008
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.649 0.640 19 41353016 missense variant G/A;C snv 0.020 1.000 2 2009 2013
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.649 0.640 19 41353016 missense variant G/A;C snv 0.030 0.333 3 2004 2017
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.649 0.640 19 41353016 missense variant G/A;C snv 0.020 1.000 2 2016 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2009 2009
Obesity
CUI: C0028754
Disease: Obesity
1111 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2010 2010