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.
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
Erythema Multiforme
CUI: C0014742
Disease: Erythema Multiforme
2 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2017 2017
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
Nephrogenic Systemic Fibrosis
CUI: C3888044
Disease: Nephrogenic Systemic Fibrosis
3 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2013 2013
Silent myocardial ischemia
CUI: C0340291
Disease: Silent myocardial ischemia
4 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2014 2014
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
Rotator cuff syndrome
CUI: C0263912
Disease: Rotator cuff syndrome
8 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2020 2020
Filarial Elephantiases
CUI: C0013884
Disease: Filarial Elephantiases
10 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2011 2011
Sarcopenia
CUI: C0872084
Disease: Sarcopenia
10 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2012 2012
Severe periodontitis
CUI: C4025886
Disease: Severe periodontitis
12 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2015 2015
Keloid
CUI: C0022548
Disease: Keloid
15 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2012 2012
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
Osteoarthritis of the hand
CUI: C0263746
Disease: Osteoarthritis of the hand
21 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2014 2014
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
Periodontal Diseases
CUI: C0031090
Disease: Periodontal Diseases
22 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2014 2014
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
Graft-vs-Host Disease
CUI: C0018133
Disease: Graft-vs-Host Disease
25 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2016 2016
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
Pulmonary Fibrosis
CUI: C0034069
Disease: Pulmonary Fibrosis
25 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1 2018 2018
Congenital Dysplasia Of The Hip
CUI: C4551649
Disease: Congenital Dysplasia Of The Hip
27 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2015 2017
Metastatic malignant neoplasm to brain
28 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1 2015 2015
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1 2011 2011
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
Kidney Failure, Acute
CUI: C0022660
Disease: Kidney Failure, Acute
32 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2014 2014
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