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.
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.050 1.000 5 2000 2013
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2000 2015
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
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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.100 0.727 22 2003 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.100 0.727 22 2003 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2003 2008
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
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
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
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2005 2015
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
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