rs1800472, TGFB1

N. diseases: 11
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.
Otosclerosis
CUI: C0029899
Disease: Otosclerosis
11 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.040 1.000 4 2007 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.020 1.000 2 2006 2006
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.010 1.000 1 2019 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.010 1.000 1 2006 2006
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.010 1.000 1 2013 2013
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.010 1.000 1 2017 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.010 1.000 1 2012 2012
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.010 1.000 1 2018 2018
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.010 1.000 1 2011 2011
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.010 1.000 1 2019 2019
Thyroid Nodule
CUI: C0040137
Disease: Thyroid Nodule
17 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 0.010 1.000 1 2009 2009