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.
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
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2019 2019
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2019 2019
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2019 2019
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.700 1.000 1 2018 2018
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
63 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2018 2018
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
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2017 2017
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
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2017 2017
Wheezing
CUI: C0043144
Disease: Wheezing
54 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2017 2017
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2016 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2016 2016
Deficiency of butyryl-CoA dehydrogenase
47 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2016 2016
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
Werner Syndrome
CUI: C0043119
Disease: Werner Syndrome
71 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2016 2016
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 0.500 2 2015 2017
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
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2015 2020
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 1.000 2 2015 2019
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 0.500 2 2015 2017
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.020 0.500 2 2015 2017
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2015 2015
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2015 2015
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2015 2015