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.
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
Heart Failure, Diastolic
CUI: C1135196
Disease: Heart Failure, Diastolic
9 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2017 2017
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2019 2019
Hypocalciuric hypercalcemia, familial, type 1
CUI: C0342637
Disease: Hypocalciuric hypercalcemia, familial, type 1
58 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2005 2005
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2008 2008
Immune thrombocytopenic purpura
CUI: C0398650
Disease: Immune thrombocytopenic purpura
35 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1 2003 2003
Kidney Failure, Acute
CUI: C0022660
Disease: Kidney Failure, Acute
32 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2014 2014
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2005 2005
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2007 2007