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.
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
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2005 2005
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2006 2014
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2006 2014
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2006 2014
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
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
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2006 2006
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.030 0.667 3 2007 2014
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.030 0.667 3 2007 2014
Squamous cell carcinoma of esophagus
329 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2007 2008
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
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
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
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
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2007 2007
Peptic Ulcer
CUI: C0030920
Disease: Peptic Ulcer
25 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2007 2007
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2007 2007
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
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2008 2008
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
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 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 Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.030 1.000 3 2010 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2010 2018