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.
Osteoarthritis, Spine
CUI: C2350242
Disease: Osteoarthritis, Spine
2 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2000 2000
Renal Insufficiency
CUI: C1565489
Disease: Renal Insufficiency
42 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2000 2000
Spondylarthritis
CUI: C0949690
Disease: Spondylarthritis
23 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2000 2000
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2001 2001
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
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
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2001 2001
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2002 2002
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2002 2002
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
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
Obesity
CUI: C0028754
Disease: Obesity
1111 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2003 2003
Polycystic Kidney, Autosomal Dominant
CUI: C0085413
Disease: Polycystic Kidney, Autosomal Dominant
35 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1 2003 2003
Adenomatous Polyps
CUI: C0206677
Disease: Adenomatous Polyps
20 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2004 2004
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
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2004 2004
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2005 2005
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
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
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2003 2006
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
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