rs121912666, TP53

N. diseases: 13
Source: BEFREE ×
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.
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
37 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.820 1.000 2 1990 2018
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
769 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.710 1.000 1 2016 2019
Squamous cell carcinoma of the head and neck
171 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.710 1.000 1 2007 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1571 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.040 1.000 4 2005 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 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
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
238 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
236 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
67 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2014 2014