rs28934575, TP53

N. diseases: 37
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.
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2002 2002
Glioma
CUI: C0017638
Disease: Glioma
353 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Liver and Intrahepatic Biliary Tract Carcinoma
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
73 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Microvascular Angina
CUI: C0206064
Disease: Microvascular Angina
10 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2012 2012
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Sarcoma of liver
CUI: C0345906
Disease: Sarcoma of liver
1 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 1997 1997
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Undifferentiated (Embryonal) Sarcoma
CUI: C0855073
Disease: Undifferentiated (Embryonal) Sarcoma
4 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 1997 1997