rs1982073, TGFB1

N. diseases: 32
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.
Rheumatic Heart Disease
CUI: C0035439
Disease: Rheumatic Heart Disease
33 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2016 2016
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2013 2013
Squamous cell carcinoma of oropharynx
CUI: C0280313
Disease: Squamous cell carcinoma of oropharynx
33 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2018 2018
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2010 2010
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2013 2013
Vesico-Ureteral Reflux
CUI: C0042580
Disease: Vesico-Ureteral Reflux
23 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2008 2008
Vesicoureteral Reflux 1
CUI: C4551858
Disease: Vesicoureteral Reflux 1
10 0.649 0.640 19 41353016 missense variant G/A;C snv 0.010 1.000 1 2008 2008