rs1800471, TGFB1

N. diseases: 48
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
2793 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.030 1.000 3 2013 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.030 1.000 3 2013 2019
Brucellosis
CUI: C0006309
Disease: Brucellosis
30 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.020 0.500 2 2015 2020
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.020 0.500 2 2012 2019
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.020 1.000 2 2002 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.020 1.000 2 2006 2006
Renal Insufficiency
CUI: C1565489
Disease: Renal Insufficiency
42 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.020 1.000 2 2000 2015
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.020 0.500 2 2012 2012
Alcoholic Liver Diseases
CUI: C0023896
Disease: Alcoholic Liver Diseases
20 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2008 2008
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2016 2016
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2013 2013
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2007 2007
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2015 2015
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2015 2015
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2006 2006
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2009 2009
Chronic interstitial nephritis
CUI: C0238304
Disease: Chronic interstitial nephritis
1 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2015 2015
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2015 2015
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2005 2005
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2019 2019
Duodenal Ulcer
CUI: C0013295
Disease: Duodenal Ulcer
33 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2007 2007
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2015 2015
Focal glomerulosclerosis
CUI: C0017668
Disease: Focal glomerulosclerosis
50 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2004 2004
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2014 2014
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2015 2015