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.
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
329 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Undifferentiated (Embryonal) Sarcoma
4 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.010 1.000 1 1997 1997
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.740 1.000 6 2006 2018
LI-FRAUMENI SYNDROME 1
CUI: C1835398
Disease: LI-FRAUMENI SYNDROME 1
39 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 19 1992 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 30 1990 2017
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
206 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.810 1.000 52 1990 2017