rs121912666, TP53

N. diseases: 34
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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.030 1.000 3 2010 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.030 1.000 3 2010 2019
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2019 2019
Leukemia secondary
CUI: C0856053
Disease: Leukemia secondary
4 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2017 2017
Liver and Intrahepatic Biliary Tract Carcinoma
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
73 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2019 2019
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2019 2019
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2004 2004
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2004 2004
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2014 2014