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.
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 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
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
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
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
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
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
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
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
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
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
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