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.
Uterine Carcinosarcoma
CUI: C0280630
Disease: Uterine Carcinosarcoma
80 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
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
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
158 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
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
Serous cystadenocarcinoma ovary
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
99 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
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
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
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 0
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
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
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
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
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
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
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
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
Li-Fraumeni-Like Syndrome
CUI: C2675080
Disease: Li-Fraumeni-Like Syndrome
8 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 0
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
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
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
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016