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.
ADRENOCORTICAL CARCINOMA, HEREDITARY
CUI: C1859972
Disease: ADRENOCORTICAL CARCINOMA, HEREDITARY
7 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7
CUI: C3553606
Disease: BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7
7 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Choroid Plexus Papilloma
CUI: C0205770
Disease: Choroid Plexus Papilloma
17 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
GLIOMA SUSCEPTIBILITY 1
CUI: C2750850
Disease: GLIOMA SUSCEPTIBILITY 1
14 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Malignant neoplasm of large intestine
CUI: C0346629
Disease: Malignant neoplasm of large intestine
375 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Sarcoma
CUI: C1261473
Disease: Sarcoma
42 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
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
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
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
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
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
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
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
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
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
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
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
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
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