rs11540652, TP53

N. diseases: 57
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.
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
206 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.800 1.000 15 1991 2015
LI-FRAUMENI SYNDROME 1
CUI: C1835398
Disease: LI-FRAUMENI SYNDROME 1
39 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 12 1992 2013
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.770 1.000 9 2012 2020
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 7 2001 2017
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.710 1.000 5 2014 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.050 0.800 5 1993 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.040 1.000 4 2010 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 3 2004 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 3 1998 2016
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.020 1.000 2 2013 2017
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.020 1.000 2 2012 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.020 1.000 2 2015 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.020 0.500 2 1993 2019
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.020 1.000 2 2013 2017
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.720 1.000 2 2013 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.720 1.000 2 2012 2015
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.020 0.500 2 1993 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.020 0.500 2 1993 2019
Triple Negative Breast Neoplasms
CUI: C3539878
Disease: Triple Negative Breast Neoplasms
99 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.020 1.000 2 2015 2018
Triple-Negative Breast Carcinoma
CUI: C4722518
Disease: Triple-Negative Breast Carcinoma
96 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.020 1.000 2 2015 2018
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 1 2016 2016
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.010 1.000 1 2012 2012
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 1 2016 2016